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The Big TEGO

Products Services Data Sheets


The Big TEGO
The ultimate reference for the paint
and coatings industry

4th revised edition 2014


Content

Editorial4 Technical Background 42


Conversion Tables 44
Portrait8 TEGO Product Groups 48
TEGO Brand within Evonik 10 Additives
TEGO and Environment Defoamers 50
TEGO Regulatory Product Finder 12 Deaerators 60
REACH on Track 13 Slip and Flow Additives,
Resource Efficiency 14 Radiation-Curing Additives 68
TEGO Tools 18 Substrate Wetting Additives 76
Global Networking 20 Wetting and Dispersing Additives 84
Your Contact Partners Worldwide 22 Rheological Additves 96
Imprint 23 Hydrophobing Agents 106
Co-Binders 124
Competences24 Specialty Binders
Adding Advantages 26 Silicone Resins 134
Shaping Technological Change 30 Nanoresins
Competence in Synthesis 34 Silica-Nanocomposites 146
Webinars on TEGO Products 37
Analytics at Evonik 38
Product Group Co-Binders  40

page 2 The Big TEGO_Content


Straight to the point

Technical Background

Application Fields

Application Fields 156 Technical Data Sheets 218


Highlights
Architectural Coatings 158 Trademarks220
Printing Inks and Varnishes 165
Wood, Furniture and Parquet Copy & Fax Order Forms 221
Coatings 174
Industrial Coatings 182
Pigment Concentrates192
Co-Binders 196
Technical Data Sheets
Selection Tables
Architectural Coatings 198
Printing Inks and Varnishes 202
Pigment Concentrates205
Wood, Furniture and Parquet
Coatings 207
Industrial Coatings 211
Leather Coatings 213
TEGO, ADDID, SILIKOFTAL, SILIKOPHEN, SILIKOPON,
Silicone Resins 214 SILIKOPUR, NANOCRYL, NANOPOL, NANOPOX,
Co-Binders 215 ALBIDUR, ALBIFLEX, SIPERNAT, AEROSIL, VESTANAT,
DYNASYLAN are registered trade marks of Evonik Industries AG
Silica-Nanocomposites 216 or one of its subsidiary companies and they are written in capital letters.

The Big TEGO_Content page 3


page 4 The Big TEGO_Editorial
Dear Reader,

The old adage goes: Great oaks from little acorns grow and youve surely
experienced the truth of this and can recall plenty of examples. It is often the
small things, the things you barely notice or perceive, that make the difference.

For example, spices improve the flavor of The coatings and printing ink industries
our food and greatly contribute to our are important target markets for Evonik.
enjoyment of it. Similar remarks apply to Always on top of technological advances,
many of Evonik's TEGO products in the Evonik can help customers develop
coatings and printing ink industries. scratch-resistant coatings for cars, wood
Added to paints, coatings, and printing flooring, and even cell phones or wall
inks, often only in small quantities, they paints that do not soil easily or contain
substantially improve the quality and per- self-cleaning mechanisms. There are even
formance characteristics of coating films. products with strong anti-graffiti effects
That's the meaning of our motto: Adding which prevent adhesion of spray paint or
Advantages, which youve been seeing on help remove it easily.
all our communications since early 2011.

The Big TEGO_Editorial page 5


In the area of coating materials, Evonik is Evonik products. Our additives also help TEGO co-binders are distinguished by a
represented in almost all product classes. protect the environment by effectively particularly wide property spectrum. In
Our leading market positions are secured reducing the use of solvents or allowing many coatings and printing inks, they
through our research and development. replacement of solvents with water, as in improve drying behavior, flexibility, and
We demand and promote a lively the case of defoamers and deaerators. adhesive strength in addition to increasing
exchange of information between special- Many of today's waterborne coatings film hardness and gloss.
ists of the individual business lines that would not exist without the use of our
supply the coatings industry. Time and additives. With last years introduction of silica-
again, this has allowed joint projects with nanocomposites, Evonik brought a new
customers to develop solutions that a unit In the area of specialty binders such as product group to its portfolio. This line is
working in isolation would have struggled silicone resins, Evonik has once again distinguished primarily by improved abra-
to achieve. This is one of Evonik's great attracted attention through its innova- sion resistance combined with high trans-
strengths. tions. While the focus was initially on parency in applications such as wood and
heat-resistant coatings for bakeware, plastic coatings.
As previously mentioned, TEGO products today's applications go far beyond the
are often used in very small quantities, kitchen. Silicone resins are now also used But it isn't just our innovative products
usually in proportions of less than one as waterproofing agents in exterior wall that you can rely on: our employees in
percent, as in the case of TEGO additives. paints and as corrosion protection coat- sales and application technology also
Despite their small presence in formula- ings. The use of specialty silicone hybrid offer outstanding customer service. Our
tions, their action is usually crucial. Many resins allows production of many indus- experts would be happy to help answer
advanced coating techniques would be trial coatings of particularly low solvent your questions about products and formu-
inconceivable without the use of these content. lations. We are prepared to develop or

page 6 The Big TEGO_Editorial


optimize coating formulations jointly with Please continue to place your trust in us.
you in any of our 11 applied technology Give us your feedback on our products
service centers around the world. Innova- and services. In this way we can continue
tion and service are what Evonik's been to improve and exceed your expectations.
offering under the TEGO brand name for
27 years. The 4th edition of the TEGO Journal, with
the new title The Big TEGO, that you're
We are convinced that innovative power now reading collects the most important
and creativity will continue to remain the information on TEGO products. The
cornerstones of our future partnerships mechanisms of action of our additives,
with you, our customers. Our investment specialty binders, co-binders, and of the
in a new laboratory building in Essen and silica-nanocomposites are explained
the initiation of R&D activities in Asia with detailed technical information. Our
underscore this belief. In conjunction product highlights showcase the most
with you, we're always on the search for important products in individual fields of
future-oriented solutions. And in this application, while the product recommen-
endeavor, we focus primarily on that dation tables simplify your search for the
which matters the most to people: envi- optimal active agent for your systems. In
ronmental compatibility and conservation addition, a selection of technical data
of resources such as energy and raw sheets affords an overview of the techni-
materials. cal properties of our products. You'll also
find contributions on the subject of
Communicating with you in depth is resource efficiency and various articles
important to us; this correspondence presenting our spectrum of expertise.
allows us to understand market needs,
customer motivations, and innovation I hope you find The Big TEGO to be a
projects. It makes us think actively about great resource. Ideally, it will make your
what markets and consumers expect for work easier and provide valuable sugges-
the future and how we can support our tions to help you meet the challenges you
customers today in developing their face. And, of course, that TEGO products
technologies of tomorrow. will continue to be your number one
choice in the future.
I would like to thank all those who have
given us the opportunity for open dia-
logue. Their readiness to enter into a Yours sincerely
trusting working relationship with us has
greatly contributed to our mutual growth.
We have been happy to take up their sug-
gestions for product development and have Dr. Dietmar Schaefer
implemented these wherever possible. Managing Director

The Big TEGO_Editorial page 7


page 8 The Big TEGO_Portrait
Portrait

The Big TEGO_Portrait page 9


The TEGO Brand within Evonik
Evonik Industries, one of the worlds leading specialty chemical companies, is active
in more than 100 countries. Creativity, specialization, continuous self renewal and
reliability are the hallmarks of the companys performance.

In the specialty chemicals sector, Evonik In 2010, Evonik generated 80% of its
concentrates on high-growth megatrends sales from leading market positions. The
especially health, nutrition, resource operational activities are divided into
efficiency, and globalization and on three segments: Consumer Health &
entering attractive future-oriented mar- Nutrition, Specialty Materials and
kets. Chemical products from Evonik are Resource Efficiency. Two business units
used in the most diverse products and which act as entrepreneurs in the enter-
industries. prise are attached to each segment.

page 10 Portrait_TEGO brand within Evonik


The Consumer, Health & Nutrition seg- With its wide product range, the Coatings As one of the four business lines within
ment serves customers from the con- & Additives business unit serves compa- the Coatings & Additives business unit,
sumer products, animal feed and pharma nies in the coatings, printing inks, adhe- Coating Additives and its TEGO brand
industries and produces specialty chemi- sives and sealants industries. Further- name stand for additives, specialty- and
cals for selected industrial markets. The more, the business unit develops co-binders as well as nanoresins. In the
segment comprises the Consumer Spe- customized functional polymers for oil Coating Additives business line, Evonik
cialties as well as the Health & Nutrition additives and binders. In the Coatings & offers the coatings and printing inks
business unit. Product-based activities Additives Business Unit, Evonik is active industry a unique range of products
relating to polymeric materials and their world-wide in 24 production and tech- the result of over 27 years of experience
precursors as well as additives are con- nology facilities. The business unit has during which the unit researched and
centrated in the Specialty Materials 4 business lines, each occupying a leading developed optimum solutions together
segment. The segment contains the Per- position in g
lobal markets: Crosslinkers, with and for its customers. With over
formance Polymers and Advanced Inter- Coating Additives, Coating & Adhesive 200 products, the range now comprises
mediates business units. Resins and Oil Additives. With its supe- not only deaerators and defoamers but
rior products, innovations, applicational also wetting and dispersing additives,
The third segment, Resource Efficiency, expertise and global distribution network, flow additives, radiation-curing additives,
offers solutions for efficient utilization of Coatings & Additives offers its customers substrate wetting additives, rheological
natural resources. Both the Inorganic all over the world a highly attractive additives and hydrophobing agents as
Materials and Coatings & Additives busi- package. well as co-binders, specialty binders and
ness units are attached to this segment. nanoresins for use in waterborne, UV
and solventborne coatings.

Portrait_TEGO brand within Evonik page 11


TEGO and Environment

TEGO Regulatory Product Finder the TEGO helps to get an overview:


search engine for products which con-
form to guidelines You will find the TEGO Regulatory Prod-
uct Finder at www.tego.de. This search
Consumer and environmental protection engine offers quick and easy access to the
are increasingly important. To meet this recommendations for additives and prod-
challenge various governments have ucts according to the current guidelines.
issued regulations and guidelines. Many
consumer-oriented companies have also Of course our experts in product safety
formulated their own standards. will be pleased to help you further with
problems concerning "TEGO Additives/
As the regulations are not harmonized, Resins and Guidelines".
manufacturers of coatings and printing
inks must take care to conform to the
guidelines appropriate to their market.

page 12 Portrait_TEGO Regulatory Product Finder


REACH on track

For the many problems which can be c onditions for continued marketing of
solved by additives, there are suitable our products. We can now concentrate
TEGO products. The implementation of on registration within the legally defined
REACH regulations, therefore, poses a time limits. As partners with our custom-
particular challenge for Evonik. ers, it is also our aim to ensure reliable
delivery of our products.
Considerable staff time and effort has
enabled us to introduce the necessary
measures early, to our customers satisfac-
tion. With the successful conclusion of
pre-registration, we have created the

Portrait_REACH on track page 13


In recent years, there have been various aim: environmentally responsible use of
attempts by the coatings industry to find raw materials, production processes, and
a response to the general trend towards applications right through to disposal
ecological responsibility. There has been without compromising technological
a general consensus with regards to the advancements or product quality.

Resource Efficiency

Various paths have been explored by the The comprehensive term Resource
coatings industry to achieve ecological Efficiency covers many aspects, and the
responsibility. For example, using renew- theme is of major importance at Evonik.
able raw materials and testing product So much so that it is reflected in the title
biodegradability has proven useful. of one of the three reporting units of the
Evoniks strategy of Resource Efficiency Evonik Group. The Evonik business lines
is an additional way of dealing with this in the coatings field are part of this
issue in the coatings field. reporting unit. A further description of
how we contribute to Resource Efficiency
is discussed in the following section.

page 14 Portrait_Resource Efficiency


Coatings have two important functions:
to produce a visual impression and to pro-
tect substrates. In both cases, the more
efficiently these functions can be achieved
the less paint is necessary, thus lowering
the consumption of resources. The term
Resource Efficiency comprises more than
that. For instance, the better the coating,
the more efficiently the object will be
protected which prolongs its life. In this
case, the complete view encompasses
more than the raw materials used in the
manufacture and application of the paint.
TEGO Airex fewer pinholes, less which would otherwise not be viable
The resources used in manufacturing the corrosion industrially. Many slow-maturing hard-
coated object must also be considered. woods naturally have a fine grain with
For example, a few hundred micrometers Microfoam and pinholes are not just few pores.
thicker corrosion protection significantly blemishes on a coat of paint. The thinner
extends the life of an extremely heavy film at these weak points also drastically To coat these without defects is state of
steel bridge. Therefore, the raw materials reduces the protection. Often, on coated the art nowadays. With demand increas-
and energy expended in manufacturing metal showing no sign of obvious dam- ing rapidly all over the world, it has for
the bridge are more efficiently used. age, the first rust originates from these many years been necessary to resort to
deaerating defects which are only a few faster-growing species of wood which
The aim of Evonik products in the TEGO tenths of a millimeter in size. often have large surface pores. Optimally
brand is to enable our customers to for- formulated coatings are essential to effec-
mulate outstanding paints and coatings. The field of corrosion protection shows tively wet such woods so that windows or
Thus our additives, specialty- and co- more clearly than any other the effect of doors manufactured from them are of
binders help modern coating systems to perfectly matched additives on the func- high quality and durability. TEGO addi-
protect natural resources. The following tion of the entire coating and therefore on tives contribute to formulating these
examples illustrate this. the protection and life of valuable objects. coatings.

TEGO Airex products extend the choice


of usable substrates. Together with very
effective and quick substrate wetting
additives from the TEGO Wet range,
they enable species of wood to be coated

Portrait_Resource Efficiency page 15


TEGO Wet only where a paint wets TEGO Foamex - combats foam ble time and energy during the dispersion
can it also protect and makes waterborne formulations process. The TEGO brand offers a par-
possible ticularly broad range of dispersing addi-
When a paint whether waterborne or tives for waterborne coating systems and
solventborne is applied to a substrate, In the change to waterborne formulations, thereby supports the trend from solvent
the interfacial surface tension determines a further difficulty must often be over- to waterborne formulations.
if it contracts or if it forms a continuous come the occurrence of foam. The
film. TEGO Wet products help to ensure TEGO Foamex range assists in prevent-
the outcome is to our customers advan- ing foam both during manufacture and TEGO Rad for emission-free, long-
tage. Here too, the effect on the protec- application of the paint. The change from lasting UV curing systems
tive action of the coating can be seen. A solventborne to waterborne formulations
coating can only effectively protect if it was first made possible by the use of Radiation-curing systems are a prime
dries without imperfections or wetting these TEGO products. Avoiding foam example of resource efficiency. TEGO
defects. during paint manufacture makes more Rad products are exactly right for formu-
efficient use of the dispersion energy and lations without solvents or water. TEGO
The contribution of TEGO Wet additives guarantees defect-free paint films on Rad products contain only materials
to conserving resources goes much fur- application. which will form the finished coating after
ther. Water, the ecologically-friendly sol- application. The improvements they pro-
vent, has a much higher surface tension duce include increased surface slip and
than organic solvents and this means that TEGO Dispers high color strength better substrate wetting. Additionally, as
wetting problems frequently occur when with low energy expenditure they are chemically incorporated during
changing from solventborne to the more curing, they remain effective long-term.
ecologically-friendly waterborne formula- The TEGO Dispers range enables color
tions. TEGO Wet additives lower the pigments (which are often expensive) to
surface tension sufficiently to permit the be used as efficiently as possible. Because
change to waterborne systems without they can produce rapid pigment wetting,
compromising the quality of the coating. TEGO Dispers products also save valua-

page 16 Portrait_Resource Efficiency


TEGO Phobe reliable protection of Specialty Binders Silicone resins for In conclusion, it can be said of all
valuable buildings high solids systems exposed to severe resources: the lower the consumption,
conditions the better for the environment. With each
Coatings incorporating TEGO Phobe new generation of products, our develop-
products protect buildings from attack by Coatings based on silicone resins protect ment work aims to reduce the amounts
moisture in the form of rain and dew. The objects under conditions where other for- required. Highly efficient additives,
combination of permeability to water mulations fail. They combine low-solvent specialty binders and co-binders even in
vapor and impermeability to water drop- formulation with great resistance to high the smallest amounts contribute in their
lets protects the building from damage. temperatures, chemicals and weathering. respective areas of application to the
TEGO Phobe products also reduce the Evonik silicone resins are a reliable, low- formulation of the best possible coating.
tendency of architectural coatings to pick solvent base for modern high solids for-
up dirt. Faades therefore remain visually mulations whether for corrosion protec- TEGO is contributing in a multitude of
attractive for longer and do not need to tion in a maritime environment or coating ways to resource efficiency in the coat-
be re-painted as often. This also saves automobile parts which must withstand ings field.
resources. temperatures of several hundred degrees
Celsius.

Co-Binders ensuring adhesion of the


protective coating Silica-Nanocomposites small partic-
les, big effect
Excellent adhesion to the substrate is
essential if a coating is to effectively fulfill Liquid silica-nanocomposites improve the
its protective function. Co-binders of the scratch and abrasion resistance as well as
TEGO AddBond and TEGO VariPlus the barrier properties of coatings. At the
ranges improve adhesion on numerous same time, they reduce the shrinkage of
surfaces and thereby anchor the protec- the coating. These characteristics contribute
tive coating to the substrate. to a markedly longer life for the coating.

Portrait_Resource Efficiency page 17


TEGO Tools
The Big TEGO The Little TEGO App
The Big TEGO is among the most impor- The mobile version of our concise refer-
tant TEGO tools available. With more ence work contains amongst others an
than 300 pages, it provides comprehen- integrated collection of formulas which
sive information on the various TEGO enable important parameters and data
products and a detailed insight into their to be calculated immediately. Detailed
background and function. Now available photos show common coatings defects.
in eight languages, it also offers selection Advice on hazards and safety rounds off
tables and technical information sheets as this attractive source of information.
well as a number of interesting reports The App is available free of charge from
and contributions on various topics. the iTunes Store and Android Market.

The Little Tego Brochures and other general descrip-


Our small, compact reference work fits tive material, flyers
comfortably into the pocket of your lab The various general brochures and flyers
coat and so is always at hand. It offers an provide an overview of the TEGO product
extensive collection of information to range. They present the highlights of
support you in your daily work. In addi- TEGO products and offer information on
tion to various formulas, conversions, and their diverse areas of application.
standards, you will find information on
topics such as paints and color, raw mate- Product Overview
rials, and typical coating defects. The Lit- The TEGO Product Overview offers a
tle Tego also includes a coatings glossary detailed survey of the different product
in five languages. groups and individual products. You'll
also find information here on the use of
the products in various fields of applica-
tion.

page 18 Portrait_TEGO Tools


Brochures for specific application areas TEGO Talk and TEGO Mail Smart Formulating Journal
These various brochures give selective The TEGO Talk and TEGO Mail newslet- The Smart Formulating Journal gives
information on TEGO additives for the ters bring you regular information on new you an excellent overview of all Evonik's
specific application areas of printing inks products and technical developments, activities in the paints and coatings mar-
and coatings as well as building protection summarizing for you the latest news of ket. The content is not restricted to the
coatings. the TEGO product range. These newslet- TEGO product range, but extends also to
ters also inform you about our trade show all other Evonik Group products in the
Internet exhibits. In this way, you're always kept area of paints and coatings. Twice a year,
On the TEGO internet website, you'll find a right up to date on the various TEGO for example, the Journal reports on cur-
wide variety of options for obtaining com- products. rent developments in Evonik's Coatings
prehensive information on all TEGO prod- unit, covering all coating components.
ucts. Apart from detailed product over- Not yet subscribed to TEGO Talk or The Smart Formulating Journal is also
views and other texts highlighting various TEGO Mail? You can order the news available on the internet at
aspects, the website offers you the oppor- letters via the Products menu item in the www.smartformulating.com.
tunity to order samples and download tech- download area at www.tego.de. And of
nical data sheets, safety data sheets and course you're always welcome to contact TEGO Sample Rack
suggested formulations. The product finder TEGO Sales Support. The TEGO Sample Rack displays TEGO
quickly directs you to the latest product rec- sample bottles to best effect. Every
ommendations. You'll also find useful infor- TEGO Tip sample bottle has its own place on this
mation on the company and discover the With every sample dispatch we include a practical rack and is readily located. The
varied application areas of TEGO products. TEGO Tip. Every month, this flyer fea- custom designed rack is easily installed
Visit us at www.tego.de. We're looking tures a different product and gives you and an attractive eye-catcher in every
forward to seeing you there! useful information on its properties and workplace. Lists of the most important
uses. samples for every application area are
Further information on Evonik products available for the rack.
specifically for the paints and coatings
market is available at www.smartformu-
lating.com.

Portrait_TEGO Tools page 19


Global networking a foundation for
success
Successful people usually have a large, Of the most importance to us are the net-
intensive network of social relationships. works with our customers and raw-mate-
Networking is a methodical, systematic rial suppliers which allow us to collect and
procedure for forming contacts, cultivat- understand information about customer
ing relationships and maintaining them requirements and changes in the market.
long-term. The aim includes the inter- Partnerships are important particularly in
change and mutual promotion of inter- the innovation process so that new, open
ests. and creative solutions can be found.

People with an effective network Here, networking of TEGO with Evonik's


achieve their goals more quickly in research resources plays a decisive role.
both their professional and private life. Access to the Evonik Chemicals Business
This is also true for us. Area's key technologies and know-how
provides an ideal basis for a quick
A comprehensive, focused worldwide response to market demands for innova-
network of contacts is the foundation for tive products and concepts.
the long-term success of TEGO. The
interface with our customers plays a cru- Effective networks are not measured by
cial role. Thus in the "Contacts" section of size alone but also by their structure. The
this "Big TEGO" alone there are some 80 network of relationships should not be
contacts that is 80 opportunities to dis- too complex at the crucial points. Along-
cuss your concerns with experts. side tailor-made courses for customers,
our philosophy includes close cooperation
Networking also plays a remarkable role with agents, distributors and the end-
in innovation. We are always fine-tuning users. Of course, this involves joint cus-
our internal networks to encourage crea- tomer visits and a mutual exchange of
tive innovation. Instilling a corporate cul- information and knowledge.
ture which encourages a willingness to
learn and the shortening of paths by
which information is circulated are impor-
tant factors.

Seite 20 Portrait_Global Networking


Our Sales Support Department rounds printing inks, our communication
out customer and partner relations man- network is also multidimensional.
agement. A team of international, multi- Involvement of customers so that they
lingual colleagues guarantees effective feel an integral part of the partnership
communication with our customers. is key to us.

Just as three-dimensional networks of Become part of our network


binder molecules are often the basis for it is worth it!
the unique properties of coatings and

Portrait_Global Networking Seite 21


Your Contact Partners Worldwide
Europe Liane Lauer Andrew Gent Valerio Restelli
Phone +49 511 2133596 Phone +44 7980172415 Phone +39 3483663774
Austria fax +49 511 2133828 fax +44 1642279503 valerio.restelli@evonik.com
Eric Godden liane.lauer@evonik.com andrew.gent@evonik.com
Phone +32 3 8257344 Turkey
fax +32 3 8283944 Martin Spahn Poland Ebru Pilavc
eric.godden@evonik.com Phone +49 6051 9779747 Robert Styrzynski Phone +90 216 395-9961
fax +49 6051 9779747 Phone +48 42 71536-10 fax +90 216 395-9650
Belarus martin.spahn@evonik.com fax +48 42 71536-05 ebru.pilavci@evonik.com
COOO Tecom-Chemie robert.styrzynski@evonik.com
Phone +375 172 984-214 Burghard Wunderlich Begm Erel
fax +375 172 984-215 Phone +49 2151 564084 Remigiusz Debczak Phone +90 216 395-9961
o.petrashko@hsh-chemie.com fax +49 2151 564085 Phone +48 42 7151168 fax +90 216 395-9650
burghard.wunderlich@evonik.com remigiusz.debczak@evonik.com begum.erel@evonik.com
Belgium
Eric Godden Great Britain Portugal Ukraine
Phone +32 38257344 Neil Cordwell Horquim-Representaes, Lda. Tecom ltd.
fax +32 38283944 Phone +44 161 7629773 Phone +351 22 967-0496 Phone +380 44 248-1225
eric.godden@evonik.com fax +44 161 7629773 fax +351 22 967-3287 fax +380 44 248-1226
neil.cordwell@evonik.com horquim@horquim.pt s.kostrov@hsh-chemie.com
Dirk Werckx
Phone +32 11271744 Andrew Gent Romania
fax +32 11851844 Phone +44 7980172415 HSH Chemie SRL NAFTA
dirk.werckx@evonik.com fax +44 1642279503 Phone +40 21 313-7778
andrew.gent@evonik.com fax +40 21 315-7864 Canada
Bosnia and Herzegovina v.zamfir@hsh-chemie.com Evonik Goldschmidt Corporation
Parka distribucija d.o.o. Dr. Benjamin Stiefvater-Thomas Phone +1 905 319-4186
Phone +385 14612-095 Telefon +44 1772 432 395 Russia fax +1 905 633-7553
fax +386 14612-098 Telefax +49 6921 868 005 Evgeny Averin asktego@evonik.com
info.hr@parkagroup.com benjamin.thomas@evonik.com Phone +7 495 72128-62
fax +7 495 72128-52 Mexico
Bulgaria Hungary evgeny.averin@evonik.com Evonik Degussa Mxico, S.A. de C.V.
HSH Chemie EOOD HSH Chemie Kft. Phone +52 555 483-1004
Phone +359 2808-8285 Phone +36 1 450-3229 Republic of Serbia fax +52 555 673-6649
fax +359 2808-8260 fax +36 1 450-3229 Parka d.o.o. asktego@evonik.com
m.shivarova@hsh-chemie.com m.nemeth@hsh-chemie.com Phone +381 1122 87560
fax +381 1122 72790 USA
Croatia Italy nenad.stojmenovic@parkagroup.com Evonik Corporation
Parka distribucija d.o.o. Gianmarco Brugnoli Phone +1 800 446-1809
Phone +386 45022-810 Phone +39 3386895278 Slovakia fax +1 804 541-6290
fax +386 45022-819 gianmarco.brugnoli@evonik.com HSH Chemie s.r.o. asktego@evonik.com
djuro.nenadovic@parkagroup.com Phone +420 261 223555-9
Massimo Cova fax +420 261 225971
Czech Republic Phone +39 3483663775 k.lukastikova@hsh-chemie.com Asia
HSH Chemie s.r.o. massimo.cova@evonik.com
Phone +420 2 612-23555 Slovenia Australia (Sydney)
Valerio Restelli Parka d.o.o.
fax +420 2 612-25971 Brenntag Australia Pty. Ltd.
Phone +39 3483663774 Phone + 386 4 502-2810
k.lukastikova@hsh-chemie.com Phone +61 2 9504-2400
valerio.restelli@evonik.com fax + 386 4 502-2819 fax +61 2 9580-8045
Denmark irena.oman@parkagroup.com snairn@brenntag-asia.com
Montenegro
Martin Spahn
Parka d.o.o. Spain
Phone +49 6051 9779747 Hong Kong
Phone +381 112287560 Ramon Garriga
fax +49 6051 9779747 Evonik Hong Kong Ltd.
fax +381 112272790 Phone +34 93 362 621 591
martin.spahn@evonik.com Phone +852 2249-6100
nenad.stojmenovic@parkagroup.com fax +34 93 362 621 592 fax +852 2249-6179
Finland ramon.garriga@evonik.com sharon.ma@evonik.com
FYR Macedonia
Neil Cordwell
Parka d.o.o. Sweden
Phone +44 161 7629773 India
Phone +381 112287560 Neil Cordwell
fax +44 161 7629773 Evonik India Pvt. Ltd.
fax +381 112272790 Phone +44 161 7629773
neil.cordwell@evonik.com Phone +91 22 6723-8800
nenad.stojmenovic@parkagroup.com fax +44 161 7629773 fax +91 22 6723-8811
Andrew Gent neil.cordwell@evonik.com biju.nair@evonik.com
Netherlands
Phone +44 7980172415
Eric Godden
fax +44 1642279503 Andrew Gent Indonesia
Phone +32 3 8257344
andrew.gent@evonik.com Phone +44 7980172415 PT. DKSH Indonesia
fax +32 3 8283944 fax +44 1642279503 Phone +62 21 5297-1570
France eric.godden@evonik.com andrew.gent@evonik.com fax +62 21 5297-1571
Sylvie Baert setya.herdiany@dksh.com
Dirk Werckx
Phone +33 160823779 Switzerland
Phone +32 11 271744
sylvie.baert@evonik.com Liane Lauer PT. Evonik Indonesia
fax +32 11 851844 Phone +49 511 2133596 Phone +62 21 520-0393
Christian Cte dirk.werckx@evonik.com fax +49 511 2133828 fax +62 21 520-0392
Phone +33 474576052 liane.lauer@evonik.com mila.tandjung@evonik.com
Norway
christian.cote@evonik.com
Neil Cordwell Martin Spahn Japan (Osaka)
Germany Phone +44 161 7629773 Phone +49 6051 9779747 Evonik Japan Co., Ltd.
Evonik Industries AG fax +44 161 7629773 fax +49 6051 9779747 Phone +81 6 6644-1575
Phone +49 201 173-2222 neil.cordwell@evonik.com martin.spahn@evonik.com fax +81 6 6644-1578
fax +49 201 173-1939 katsuhiko.ishii@evonik.com
info-tego@evonik.com

page 22 Portrait_Contact Partners Worldwide


Japan (Tokyo) Egypt Greece UAE
Evonik Japan Co., Ltd. Egyptian Promoters Center Goldchem EPE Petrochem Middle East FZE
Phone +81 3 5323-7418 Phone +202 2291-8272 Phone +30 210 68-25802 Phone +971 4 417-9326
fax +81 3 5323-7397 fax +202 2415-5023 fax +30 210 68-34537 fax +971 4 417-9393
katsumi.hazama@evonik.com e.talaat@epcegypt.com goldchem@otenet.gr suresh@petrocheme.com

Korea Morocco Guatemala Uruguay


Evonik Korea Ltd. Sylvie Baert J. C. Niemann Mayerhofer Argentina S.A.
Phone +82 2 320-4761 Phone +33 160823779 Phone +502 24208989 Phone +54 11 4555-4003
fax +82 2 783-2520/30 sylvie.baert@evonik.com fax +502 23347453 fax +54 11 4554-3915
hyungwook.kim@evonik.com ksundfeld@jcniemann.com alejandro.degasperi@mayerhofer.com.ar
South Africa
Malaysia Evonik Africa (Pty) Ltd. Honduras Venezuela
Evonik Malaysia Sdn Bhd Phone +27 31 765-1658 J. C. Niemann Cenco-Zotti S.A.
Phone +60 3 2268-7908 fax +27 31 765-1658 Phone +502 24208989 Phone +58 21 2903 5250
fax +60 3 2268-7999 les.message@evonik.com fax +502 23347453 fax +58 21 2903 5302
ethan.chong@evonik.com ksundfeld@jcniemann.com nbracho@cenco-zotti.com
Sub-Saharan Africa
New Zealand Evonik Africa (Pty) Ltd. Israel
Brenntag New Zealand Ltd. Phone +27 31 765-1658 Wm. Rosenstein Ltd.
Phone +64 9 275-0745 fax +27 31 765-1658 Phone +972 9 971-8831
fax +64 9 275-0746 les.message@evonik.com fax +972 9 971-8830
kmasefield@brenntag-asia.com miri@wrl-ltd.com
Tunisie
P.R. China (Guangzhou) SAC - Socit Adly Chimic Jordan
Evonik Degussa (China) Co. Ltd., Phone +212 71 827-488 Evonik Industries Regional Office
Guangzhou Branch fax +212 71 827-466 Phone +962 6 554-9395
Phone +86 20 8215-6200 maya.bentekaya@planet.tn fax +962 6 554-9394
fax +86 20 3229-0900 neveen.kanaan@evonik.com
xuefang.chen@evonik.com
South America and Kuweit
P.R. China (Shanghai)
Other Countries Petrochem Middle East FZE Imprint
Evonik Degussa Specialty Chemicals Phone +971 4 417-9326
(Shanghai) Co., Ltd. Argentina fax +971 4 417-9393 Editor
Phone +86 21 6119-1368 Mayerhofer Argentina S.A. suresh@petrocheme.com Evonik Industries AG
fax +86 21 6119-1149 Phone +54 11 4555-4003 Goldschmidtstrae 100, 45127 Essen,
huibin.zhao@evonik.com Lebanon
fax +54 11 4554-3915 Germany
SLID S.A.L.
alejandro.degasperi@mayerhofer.com.ar
Philippines Phone +96 19 214-507 Editor in Chief
Jebsen & Jessen Chemicals (P) Inc. Bahrain fax +96 19 214-508 Wernfried Heilen
Phone +63 2 786-7700 Petrochem Middle East FZE mego.torossian@sild-sal.com Authors
fax +63 2 786-7716 Phone +971 4 417-9326 Portrait: Dr. Patrick Glckner, Wernfried
lynn_polintan@jjsea.com Oman
fax +971 4 417-9393 Heilen, Christiane Hg, Thomas Ries,
Petrochem Middle East FZE
suresh@petrocheme.com Dr. Dietmar Schaefer, Dr. Michael Schwan,
Singapore Phone +971 4 417-9326
Dr. Hans Gnther Wey
Evonik (SEA) Pte. Ltd. Brasil fax +971 4 417-9393
Phone +65 6809-6666 Evonik Degussa Brasil Ltda. suresh@petrocheme.com Competences: Marcus Freyer,
fax +65 6809-6866 Phone +55 11 3146-4124 Dr. Patrick Glckner, Wernfried Heilen,
lia.marahusin@evonik.com Pakistan Dr. Ibrahim Jussofie, Dr. Mario Lbbus,
fax +55 11 3146-4140
Dyechem Enterprises Susanne Struck
Taiwan Chile Phone +92 21 244-2180
Technical Background: Karl Bechtold,
Evonik Degussa Taiwan Ltd. CONINTER LTDA. fax +92 21 244-8701
Marcus Freyer, Dr. Sascha Herrwerth,
Phone +886 2 2717-1242 Phone +56 2 621-3859 imranbaig@dyechementerprises.com
Dirk Hinzmann, Marco Heuer,
fax +886 2 2717-2106 fax +56 2 621-1759
Peru Jrgen Kirchner, Frank Kleinsteinberg,
jeff-ct.chen@evonik.com fgonzalez@coninter.cl
IVER S.A. Kirstin Schulz, Heike Semmler
Thailand Colombia Phone +511 616-0100 Application Fields: Marcus Freyer,
DKSH (Thailand) Ltd. INCOPACK S.A. fax +511 616-0111 Dr. Sascha Herrwerth, Dirk Hinzmann,
Phone +66 2 332 4000 Phone +57 4 313-0164 gflores@iver.com.pe Frank Kleinsteinberg, Kirstin Schulz,
fax +66 2 730 3195 fax +57 4 313-4988 Heike Semmler, Kai Steenweg
jaruwan.k@dksh.com Qatar
sebastian.jimenez@incopack.com.co
Petrochem Middle East FZE Photos
Vietnam Phone +971 4 417-9326 Andreas Hirsch, Harald Reusmann
Costa Rica
Viet Hoa Sinh Co., Ltd. J. C. Niemann fax +971 4 417-9393 Illustrations
Phone +84 8 3512-8128 Phone 502 24208989 suresh@petrocheme.com MERZ Werbeagentur GmbH, Dsseldorf
fax +84 8 3512-7127 fax +502 23347453
Saudi Arabia Concept
ngoclien@biochem.com.vn ksundfeld@jcniemann.com
Petrochem Middle East FZE Evonik Industries AG
Ecuador Phone +971 4 417-9326 Design
Africas Minerva S.A. fax +971 4 417-9393 MERZ Werbeagentur GmbH, Dsseldorf
Phone +593 2 247-9329 suresh@petrocheme.com
Translation
Algrie fax +593 2 247-8115
Sri Lanka John Haim and David Hyatt
Evonik Industries AG, pdelarosa@minerva.com.ec
Bureau de Liaison Finchem (Pvt.) Ltd. Copyright
Phone +213 21 74-9212 El Salvador Phone +94 11 255-9723 All texts, photos, graphics and other
fax +213 21 64-9212 J. C. Niemann fax +94 11 2581861 material may not be published, broadcast,
said.djadel@evonik.com Phone +502 2420 8989 finchem@sltnet.lk rewritten or redistributed without
fax +502 2334 7453 permission.
ksundfeld@jcniemann.com

Portrait_Contact Partners Worldwide_Imprint page 23


page 24 The Big TEGO_Competences
Competences

The Big TEGO_Competences page 25


Adding Advantages
Additional benefits and special effects with TEGO products

For over 27 years, Tego has been a relia- benefits which are not always immedi-
ble partner with innovative solutions. ately obvious. Since these effects are as
We aim to develop with our customers different as they are diverse, we will limit
eco-friendly products for new areas of ourselves at this point to describing the
application. The TEGO portfolio comprises characteristics generated by our TEGO
various product groups which generate Glide additives.
different effects to improve the properties
of coatings for widely differing uses in the It is generally accepted that the use of
coatings industry. surface-active additives in coatings is nec-
essary to smooth out all the irregularities
Our additives, such as hydrophobing caused by the topography of the substrate
agents, specialty binders and co-binders or by the application process.
can provide our customers with additional

page 26 Competences_Adding Advantages


Surface active additives include modified depend on whether the side chains are by the formation of surface tension gradi-
siloxanes derived from low molecular statistically distributed along the polysi- ents which frequently hinder the genera-
weight polydimethyl siloxanes in which loxane chain (comb-like structure), tion of a smooth surface. One cause is
individual methyl groups are replaced by whether a block structure is present or evaporation of the solvent used in paints.
a variety of organic side chains such as the polysiloxane chain is only terminally
polyethers. Usually they are products with modified. The way the polyether side The term smooth can be used in two
a molecular weight range between 1,000 chain is attached to the basic polysiloxane ways when referring to paint surfaces.
and 15,000 g/mol. In principle, the prop- framework is also important. On the one hand, it can describe a surface
erty profile of modified siloxanes is which is texture (pitting) free. Smooth
dependent on their silicone content, the Silicone additives are often mentioned in can also describe the slip characteristics
structure of the siloxane backbone and the paint industry and many formulators and is then a measure of the frictional
the side chains. associate these with cratering which can resistance or sliding resistance of the
be caused by silicone oils. Although poly- surface.
Polyethers are generally made up of eth- ether siloxanes differ considerably from
ylene oxide units (EO) and propylene silicone oils, the use of this product group To obtain a smooth surface, free of tex-
oxide units (PO). Polyethylene oxide is is frequently avoided. Modification by our ture which also exhibits a low frictional
very hydrophilic (polar), polypropylene polyether chemistry is, however, the key resistance, surface flow control additives
oxide, in contrast, is hydrophobic (non- factor to rule out such cratering. are used in both waterborne and solvent-
polar). The polarity can thus be adjusted borne paints.
via the EO/PO ratio. Besides the EO/PO Insufficient flow in the applied paint film,
ratio of the polyether and the number of particularly in the interval between appli-
polyether chains, properties essentially cation and curing is thought to be caused

Competences_Adding Advantages page 27


These surface-active additives can Thus products which improve substrate Air-draught sensitivity, which occurs fre-
improve more properties than is initially wetting have an amphiphilic structure, quently especially when applying wood
apparent, including: i.e. the molecule contains hydrophilic and coatings using curtain coating equipment,
inadequate substrate wetting hydrophobic parts, giving them the ability can be avoided by using alkyl-modified
cratering caused by spray mist or dust to orient themselves to the interface. siloxanes. Such products are also helpful
inclusion with regard to a more uniform orientation
air-draught sensitivity These surface-active additives have up to of the matting agent used.
ghosting seven siloxane units; the higher the pro-
Bnard cells portion of Si in the molecule, the greater The phenomenon of ghosting cannot
is its interfacial activity. always be totally eliminated but poly-
These additional benefits are achieved by ethersiloxanes with a high PO content can
modifying the silicone skeleton to suit the Prevention of cratering stems from the reduce this effect drastically.
application and also varying the chain capacity of this class of products to reduce
length. static surface tension which permits wet-
ting and coating of impurities. Spray mist
absorption is also improved.

page 28 Competences_Adding Advantages


An important relevant effect is the occur- In matted clear coats, the matting agent
rence of Bnard cells. During evaporation can play the role of the less mobile pig-
of the solvent, relatively solvent-rich (low ment. This also leads to a honeycomb
viscosity) paint with a lower density flows structure or to silking in the case of verti-
from deeper paint layers to the surface cal surfaces. With unpigmented systems,
where it spreads and the solvent evapo- irregular finishes result. Besides these
rates. As a result, the paint in the upper- differences in surface tension occurring in
most layer of the coating has a greater the paint itself, defects can also be caused
density than underlying layers and subse- by differences in surface tension between
quently sinks. substrate and coating.

During these flows, vortices occur which All these phenomena can be counteracted
may entrain pigments of differing density. with surface-active additives (TEGO
Since the viscosity of the paint increases Glide) since they maintain the surface
as the solvent evaporates, these flows tension at a uniformly low level during
come to a halt as the paint dries. In the the entire film-forming and curing
ideal case, a more or less regular hexago- process.
nal honeycomb structure forms on hori-
zontal surfaces, the so-called Bnard cells.
On vertical surfaces these cells merge into
stripes (silking).

Competences_Adding Advantages page 29


Shaping Technological Change with TEGO

As leading manufacturers of eco-friendly coatings and printing inks, we are


actively shaping technological change to meet the demand for eco-friendly
technologies which combine maximum performance, highest quality and
cost-effectiveness.

Our own commitment, as well as environ- However, not only waterborne and radia-
mental requirements, has resulted in tion-curing formulations are experiencing
many traditional solventborne formula- high growth rates. At present, the highest
tions being modified to incorporate relative growth rates are found with sol-
modern technologies. ventborne, high solids coatings.

page 30 Competences_Technological Change


Global figures give only a limited picture Even though ecological aspects are often The raw materials industry has been
as trends differ significantly from region the main concern, technological change is closely involved in implementing and
to region and which "new technology" also being driven by other demands. even initiating these changes. No matter
ultimately prevails depends strongly on whether developing solventborne high
the end use. Thus, in architectural coat- Heightened user awareness of product solids, waterborne or radiation-curing
ings, waterborne paints and coatings con- performance, quality and customization is formulations, TEGO is the right partner
tinue to be the norm with increasingly less affecting the choice of high performance to have at your side.
dependence on organic co-solvents. Up to products. Many innovations in coatings
now, radiation-curing formulations have development show that such demands With our know-how and broad portfolio
been mainly used in wood finishes and need not be inconsistent with cost effec- of innovative functional additives, co-
printing inks. tiveness. binders and specialty binders for solvent-
borne high solids, waterborne or radia-
Alongside this, growth in pigmented For example, traditional batch processes tion-curing formulations we provide you
formulations has been disproportionately are being increasingly replaced by semi- with support in the development of
high. In corrosion protection and with finished product manufacture. In coatings, modern coatings and printing inks. We
many industrial coatings, formulators are pigment concentrates allow rapid produc- contribute the critical difference which
frequently reducing VOC emissions by tion of color tints. However, pigment con- makes your formulations even more
increasing the solids content in high solids centrates are also being used in decorative successful.
and ultra high solids formulations. coatings so that end-users can individually
set "their" color tint.

Competences_Technological Change page 31


Flow and deaerating problems are TEGO has a particularly comprehensive
increasingly important when formulating portfolio of additives for waterborne
high solids coating systems. At the same coatings and printing inks. Alongside
time high pigment and filler loads pose a high-performance defoamers and deaera-
challenge to maintaining application char- tors, TEGO can offer the right products
acteristics. The lower the solvent content for the most varying demands: highly
of the formulation, the more important effective substrate wetting and anti-cra-
are powerful additives to ensure problem- tering additives improve critical wetting
free application and optimum properties behavior of waterborne formulations,
of the coating. Evonik is at the forefront in tailored flow and slip additives ensure the
this respect with its tailor-made deaera- perfect finish and modern breathable
tors, anti-crater-, flow-, wetting- and dis- faade coatings obtain their water repel-
persing additives and its continually lency from TEGO hydrophobing agents.
expanding product range.
Of course, we also have the perfect solu-
TEGO co-binders improve adhesion to tion for pigment wetting and stabilization
many metal and plastic substrates and the in the form of TEGO Dispers: no matter
mechanical properties of the coating. whether for direct grind or pigment con-
Many of these products are themselves centrates or used for industrial coatings,
"high solids" and thus solvent-free or low architectural coatings or printing inks.
in solvent thereby contributing to reduc- The portfolio is completed by tailored
tion in VOC. Evonik even has a sole co-binders, which improve the adhesion
binder, Silikopon EF, for ultra high solids and mechanical properties of waterborne
anti-corrosion coatings. coatings and allow formulation of
pigment concentrates for coatings with
maximum durability.

With TEGO, waterborne really does mean


solvent-free. We offer all these products
as concentrates, waterborne solutions or
emulsions. TEGO additives make possible
the formulation of completely solvent-
free waterborne coatings and printing
inks.

The trend to completely solvent-free


products is also apparent with radiation-
curing coatings and printing inks. The use
of solvents has either been eliminated or
reduced to a minimum even in areas of
application where they have traditionally
been used. The challenges associated with
this show up in the areas of manufacture
and above all application.

page 32 Competences_Technological Change


Rheological problems increase dramati- low-migration wetting and flow and some
cally and it becomes increasingly difficult grades also produce slip and release prop-
to ensure good substrate wetting, erties. Please enquire about our powerful,
defoaming and flow. naturally solvent-free, wetting and
dispersing additives for radiation-curing
For many years, TEGOs portfolio has formulations. Finally, a broad portfolio of
included special solvent-free additives for defoamers and deaerators eliminates foam
radiation-curing formulations and this problems in coatings ranging from
range is continuously increasing. We offer sprayed UV clear-coats to pigmented
a complete range of tailor-made radically screen printing inks.
crosslinkable surface-active additives for
radiation-curing under the TEGO Rad
brand. These ensure highly effective,

Competences_Technological Change page 33


Competence in Synthesis

We are indebted to our predecessors as their ground-breaking work and


innovations in the field of organo-modified silicones laid the foundation for
the subsequent success of Evonik Industries in the coatings and printing
inks sector.

However, we have continued to move The origins of many of our current prod-
forward and our innovations have set new ucts can be traced back to the broad
benchmarks for the development of eco- technological foundations of the former
friendly coatings systems. Here we would Goldschmidt-Chemie. Today, as part of
like to give you an understanding of the the modern specialty chemicals company
extraordinarily broad range of technologies Evonik, TEGO can draw on a vastly
on which our innovative products are greater range of chemical knowledge
based. and processes.

page 34 Competences_in synthesis


We are now experts in new methods of cone additives, offers numerous possible universal pigment pastes. Finally, new
polymerization as in the synthesis and use solutions particularly for satisfying the polyether catalysis technologies are
of ionic liquids in special applications or requirements of low-migration coatings expected to lead to numerous innovative
modern, highly selective enzyme technol- systems. products which have been inaccessible via
ogies. conventional technologies up to now.
Another key resource in the field of
As can be seen from the illustration, a key organo-modified silicones is polyether Another mainstay in our technology port-
factor is silicone technology which is used technology. This enables customized folio are functional, organic polymers
in a complex, flexible and powerful sili- polyethers to be manufactured from a used in high quality dispersing additives,
cone-composite structure in manufactur- wide range of monomers using various deaerators and flow and leveling agents.
ing and various research platforms. This production processes depending on the The intelligent linking of pigment-affinic
has permitted numerous structure, topol- subsequent application. Special allyl poly- groups (the functional groups) with a
ogy and functionalization possibilities for ethers, for example, are used as important suitable polymer architecture and the
the ever growing group of organo-modi- building blocks in the manufacture of widest possible range of polarity charac-
fied silicone products. silicone polyethers. Besides the choice terizes modern high-performance dis-
of suitable alkylene oxides, the ability to persing additives.
Expertise in manufacturing, defined build up the monomers block by block
branched siloxane structures, and control- is a decisive criterion for application Besides the traditional chemical technolo-
ling production processes is one of the properties. gies for dispersing additives, which are all
most important prerequisites for being used at Evonik, we also use modern, con-
able to manufacture high performance However, tailor-made polyethers are also trolled polymerization technologies. An
coatings additives. For example, new, used in various areas of modern additives. understanding of interfacial interactions,
innovative silicone multi-functional sur- Certain special polyethers with longer, such as the molecular adsorption processes
factants with very compact structures non-polar head groups have proved excel- on pigment surfaces, is crucial for synthe-
result in properties for substrate wetting lent organic surfactants, even under sis design, a task implemented efficiently
additives unobtainable with conventional dynamic conditions. Ionic and non-ionic at Evonik using statistical test plans.
structures. Furthermore, radiation-curing, styrene oxide polyethers, on the other
which allows chemical incorporation of hand, can be processed into high-per-
multi-functional, organo-modified sili- formance dispersing additives for use in

Competences_in synthesis page 35


Our innovative silicone resin hybrid bind- We hope that this short overview of our
ers can play an important role in the technology portfolio will show you that
search for new, modern, low-VOC, high we are one of the most versatile manufac-
solids coatings systems. Water-based pri- turers of coatings additives. New technol-
mary or secondary silicone-resin emul- ogies and resulting innovations will con-
sions are also important for our customers tinue to be an important factor.
eco-friendly coatings.

Since it is often advantageous to use addi-


tives as formulated products or multi-sub-
stance mixtures, specialist formulation
know-how is a core competence of our
research and development chemists.
Thanks to our knowledge of physical,
chemical and interfacial interactions, we
can increase the effect of defoamer con-
centrates using hydrophobic, micro-scale
solids or stabilized emulsions. Besides
commercially-available emulsifiers, we
also have our own emulsifier portfolio.

page 36 Competences_in synthesis


Webinars on TEGO Products

For many years now, we've been training tial overview of our online training offers
customers in the use of our TEGO prod- and register for our web-based training.
ucts, mainly through personal contact. Following successful registration and
However, your daily routine doesn't login, further information on individual
always leave time for seminars at which training modules will be provided.
you can be physically present.
Webinars will allow our customers
Therefore, we will be offering web-based located anywhere in the world to partici-
seminars, or webinars, enabling our cus- pate in our training modules for newly
tomers to p
articipate in online training for launched products.
newly introduced products. On our Inter-
net website www.tego.de, you will find a
webinars area, where you can get an ini-

Competences_Webinars page 37
Analytics at Evonik
The international success of a company in the chemical industry is reliant on the quality of its
products. The high demands made by customers on chemical products and product mixtures
relate mainly to purity and reproducibility in the production process. The synthesis of a new
product right through to its final stage requires reliable, modern instrumental methods of analy-
sis which can continuously monitor purity both qualitatively and quantitatively.

Evonik uses the following modern instrumental analytical methods

1. NMR: Nuclear Magnetic Resonance 2. IR: Infrared Spectroscopy 3. HPLC-NMR: High Performance
Spectroscopy This method allows several specific inves- Liquid Chromatography and NMR
This method is used to carry out structural tigations of structure: soluble and insolu- Spectroscopy
characterization of soluble organic com- ble organic compounds, special investiga- The combination of HPLC with NMR
pounds for the following: product moni- tions of fillers, qualitative and quantitative Spectroscopy allows mixtures to be
toring, batch analysis, purity (qualitative investigations of products with a detec- separated into pure fractions followed by
and quantitative), determination of end- tion limit of approx. 0.1%, surface inves- exact structural investigations using
groups, determination of chain length or tigations of a coating, investigation of cra- NMR.
degree of polymerization, determination tering on a coating, and determination of
of polymer identities and quantities in inhomogeneity of a polymer compound. 4. GC-MS: Gas Chromatography and
co-polymers, detection of silicone oil in Mass Spectroscopy
coatings, characterization and differentia- All volatile components of a mixture can
tion of a silicone oil or a polyethersiloxane be characterized using this combined
to trace levels, reaction optimization by method. Evaluation involves the use of
kinetic NMR measurements, investigation extensive software.
of products down to a detection limit of
approx. 1 ppm.

page 38 Competences_Analytics
5. LC-MS: Liquid Chromatography and 7. MALDI: Matrix Assisted Desorption 8. Organic wet chemistry
Mass Spectroscopy Ionization Effective methods for rapid determination
This method is a combination of liquid MALDI is a method for characterization of characteristic values are important.
chromatography with mass spectrometry. of biomolecules and synthetic polymers. Parameters such as hydroxyl value, acid
The chromatography separates compo- The principle involves ionization pro- value, iodine value, amine value, color
nents and mass spectrometry is used to duced using a UV laser. The polymer index, betaine concentration, and anionic-
identify and/or quantify the individual under investigation is incorporated in a and cationic-surfactant concentrations can
components. UV-active matrix. Molecular cations are be rapidly determined by wet chemical
formed. The matrix prevents molecular methods.
6. GPC: Gel Permeation fragmentation.
Chromatography The combination of all the analytical
GPC characterization of polymer samples methods which are available to us at
encompasses determination of the Evonik enables investigation of all
molecular mass distribution and average relevant chemical materials and product
molecular mass with a RI (Refractive mixtures and thus allows us to satisfy
Index) detector. Peak position calibration the demands of our customers.
is carried out using commercially availa-
ble, linear-structure standards.

Competences_ Analytics page 39


Product Group Co-Binders

TEGO VariPlus for a brilliant With the help of TEGO VariPlus, the Consequently, they are used as resins for
appearance solids content in paints can be increased. pigment pastes in coatings formulations
The hyper-branched polymer structures which cure at moderate baking tempera-
With TEGO VariPlus, Evonik offers a result in low solution viscosities which tures. Pigment loading can be increased
comprehensive range of special purpose can lead to significantly lower solvent and even at high pigment content, excel-
resins for customizing the properties of content in paints formulated with them. lent gloss can be obtained.
coatings and printing inks. Furthermore, film hardness, adhesion to
various substrates, gloss and film build TEGO VariPlus products can be used in
TEGO VariPlus are film-forming co- can be modified. solventborne formulations with low VOC
binders based on modified ketone-alde- content, waterborne or radiation-curing
hyde resins. These are widely compatible Since TEGO VariPlus products are unsa- systems.
with the most diverse binder systems and ponifiable, corrosion protection is also
solvents. improved. Some of the products are very
resistant to, for example, heat, acids and
alkali solutions and can thus improve
resistance to yellowing and chemicals.
The customized incorporation of func-
tional groups makes TEGO VariPlus well
suited for high color intensity pigment
pastes.

page 40 Competences_TEGO VariPlus


TEGO AddBond for maximum that they are also highly recommended curing or heat-curing. Broad compatibility
adhesion for use in multi-coat systems. In special is guaranteed in various binder systems
effect coatings, they improve cohesion and solvents. The product portfolio also
Under the TEGO AddBond brand name, within the film. The adhesion properties includes high solids binders enabling VOC
Evonik markets high performance pro and excellent resistance to hydrolysis of content to be lowered in paint
ducts for use as adhesion promoters in TEGO AddBond products lead to signifi- formulations.
coatings and printing inks. TEGO Add- cantly improved corrosion protection by
Bond products are based on special pur- the coating. The flexibility and hardness
pose polyesters which, because of their of the coating can also be adjusted by the
polymer structure and functional groups, various products to meet individual
are effective on different substrates. requirements.

Improved adhesion is achieved on numer- The TEGO AddBond range comprises


ous substrates (metals, minerals and plas- polyester resins for use in solventborne,
tics) and TEGO AddBond products are waterborne and radiation-curing coatings
thus frequently used in primers. Further- and printing inks. These systems can be
more, they improve intercoat adhesion so physically or oxidatively drying, radiation-

Competences_TEGO AddBond page 41


page 42 The Big TEGO_Technical Background
Technical Background

The Big TEGO_Technical Background page 43


Comparison of viscosity measurements
Dynamic viscosity

Pa s
at density 1000 kg/m3 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1

Poise 1 2 3 4 5 6 7 8 9 10

Krebs units 40 50 60 62 64 65 68 70 72 74 76 78 80 82 84 86

Kinematic viscosity

Stokes 0 1 2 3 4 5 6 7 8 9 10

A2
Gardner-Holdt A3 A1 A B C D E F G H I J K L MN O P Q R S T U V

ISO cup 25 50 75 100 125 150 175 200 225 250 275 300

BS cup B4 20 30 40 50 60 70 80 90 100 110 120 130 140 150 160 170 180 190 200

Coupe 4-NFT 20 30 40 50 60 70 80 90 100 110 120 130 140 150 160 170 180 190 200

Ford no. 4 ASTM 10 20 30 40 50 60 70 80 90 100 110 120 130 140 150 160 170 180 190 200

DIN 4 mm 53211 20 30 40 50 60 70 80 90 100 110 120 130 140 150 160 170 180 190 200

DIN 6 mm 53211 10 15 20 25 30 35 40 45 50 55 60

Zahn cup no. 2 20 40 60 80

Zahn cup no. 3 10 20 30 40 50 60

Zahn cup no. 4 10 20 30 40 50 60 70

Kinematic viscosities are only valid for liquids


with Newtonian flow and the above information
must therefore be regarded only as approximate.

page 44 Technical Background_Conversion Tables


Units
Comparison of anglo-american and metric units

Units of length Units of area

in ft yd mm m in2 ft2 yd2 cm2 m2

1 in 1 0.0833 0.0278 25.4 0.0254 1 in 2


1 6.944x10 -3
0.772x10 -3
6.4516 0.645x10-3

1 ft 12 1 0.33333 304.8 0.3048 1 ft2 144 1 0.1111 929.03 0.0929

1 yd 36 3 1 914.4 0.9144 1 yd 2
1,296 9 1 8,361.27 0.8361

1 mm 0.0394 3.281x10-3 1.094x10-3 1 1.000x10-3 1 cm2 0.155 1.076x10-3 0.120x10-3 1 0.10x10-3

1m 39.3701 3.2808 1.0936 1,000 1 1m 2


1,550 10.7639 1.1960 10,000 1

Units of volume Other units

in3 ft3 yd3 cm3 dm3 m3 1 mil = 10-3 in = 0.0254 mm

1in 3
1 0.579x10 -3
21.433x10 -6
16.3871 0.0164 16.387x10 -6
1 sq mil = 10 sq in
-6
= 645.16 m2

1ft3 1,728 1 0.037 28,317 28.3169 0.0283 1 English mile = 1,609 m

1yd 3
46,656 27 1 764,555 764.555 0.7646 1 Imp. gallon (Imperial gallon) = 4.546 l

1cm3 0.061 35.315x10-6 1.308x10-6 1 1.000x10-3 1.0x10-6 1 US gallon (United States gallon) = 3.785 l

1dm 3
61.0237 0.0353 1.308x10 -3
1,000 1 1.0x10 -3
1 stone (GB) = 14 Ib = 6.35 kg

1m 3
61,023.7 35.3147 1.3080 1,000,000 1,000 1 1 short quarter (US) = 11.34 kg

1 long quarter (GB, US) = 12.70 kg

1 short ton (US) = 0.90718 t

Units of weight

oz lb g kg t
Dispersion and grinding fineness
1 oz 1 0.0625 28.3495 0.0283 28.350x10-6

1 lb 16 1 453.592 0.4536 0.454x10-3 Hegman & NS Mils Microns

1g 0.0353 2.205x10-3 1 1.0x10-3 1.0x10-6 0 4.0 100

1 kg 35.2740 2.2046 1,000 1 1.0x10 -3


1 3.5 88.9

1t 35,274.0 2,204.62 1,000,000 1,000 1 2 3.0 76.2

3 2.5 63.5

4 2.0 50.8

5 1.5 38.1

6 1.0 25.4

7 0.5 12.7

8 0 0

Technical Background_Conversion Tables page 45


Formulary
Important formulas for the coatings formulator

PVC (Pigment volume concentration) Epoxide amine curing


VPigments + VFillers
PVC = 100% EP value x (NH) equivalent mass = g hardener per 100 g EP resin
VPigments + VFillers + VBinders

Spreading rate Mix ratio isocyanates

[= kg ]
Spreading m2 solid body [%]
NCO components proportional weight NCO components x 17 x % NCO
rate =
[ m ] x film density [m] x 100
kg OH components proportional weight OH components x 42 x % OH
dry film density 3

Isocyanates Conversion of OH-number to OH-% content:

42 OH-% content = OH-number [mg/g] x 0.0303


equivalent weight NCO components [g] = x 100
% NCO OH-% content: Weight of OH-groups in 100 g binder

17 OH-number: The weight of KOH in mg, which contains the same amount
equivalent weight OH components [g] = x 100
% OH of hydroxyl groups as 1 g of the substance. Units are [mg/g].

Epoxide isocyanate curing

Hydroxyl value EP x isocyanate-equivalent mass


= g isocyanate per 100 g EP resin

page 46 Technical Background_Conversion Tables


Temperature
Temperature Conversion Formulas

Celsius Fahrenheit Raumur

Celsius 1 1.8x + 32 0.8 x

Fahrenheit 0.56x 17.78 1 0.44x 14.22

Raumur 1.25 x 2.25x + 32 1

Conversion Table from C to F

C F C F C F C F C F C F

-40 -40 +5 41 50 122 95 203 140 284 185 365

-35 -31 10 50 55 131 100 212 145 293 190 374

-30 -22 15 59 60 140 105 221 150 302 195 383

-25 -13 20 68 65 149 110 230 155 311 200 392

-20 -4 25 77 70 158 115 239 160 320 205 401

-15 +5 30 86 75 167 120 248 165 329 210 410

-10 14 35 95 80 176 125 257 170 338

-5 23 40 104 85 185 130 266 175 347

0 32 45 113 90 194 135 275 180 356

MESH Conversion Table


Sieve fineness

Micrometre Milimetre Inch Micrometre Milimetre Inch


[m] [mm] U.S. MESH [in] [m] [mm] U.S. MESH [in]

20 0.020 635 0.0008 177 0.177 80 0.0070

37 0.037 400 0.0015 210 0.210 70 0.0083

44 0.044 325 0.0017 250 0.250 60 0.0098

53 0.053 270 0.0021 297 0.297 50 0.0117

62 0.062 230 0.0024 350 0.350 45 0.0138

74 0.074 200 0.0029 590 0.590 30 0.0232

88 0.088 170 0.0035 840 0.840 20 0.0331

105 0.105 140 0.0041 2000 2.000 10 0.0787

125 0.125 120 0.0049 4000 4.000 5 0.1570

149 0.149 100 0.0059

Technical Background_Conversion Tables page 47


TEGO Product Groups

Additives prevents defects in the coating such as All TEGO ViscoPlus products are liquid
crater formation, poor leveling or inade- and free of organic solvents and alkylphe-
Defoamers quate adhesion of the coating film. nolethoxylates. Furthermore, they are
TEGO Foamex manufactured without the addition of
Defoamers prevent formation of foam Wetting and dispersing additives organo-tin compounds.
during manufacture and application of TEGO Dispers
coatings and printing inks. Foam already Wetting and dispersing additives prevent Radiation-curing additives
formed is destroyed and air occlusions floating, flooding and sedimentation of TEGO Rad
prevented. pigments in paints, lacquers and pigment These crosslinkable additives for radia-
concentrates. They improve color tion-curing formulations increase slip and
Deaerators strength development, transparency and scratch resistance, improve flow and addi-
TEGO Airex gloss. All TEGO Dispers products are tionally prevent formation of foam.
Deaerators prevent development of air free of alkylphenolethoxylates.
occlusions and pinholes. This is particu- Multi-functional surfactants
larly important in high-viscosity and high Hydrophobing agents TEGO Twin
solids formulations and indispensable for TEGO Phobe The unique technology of the TEGO
airless-/airmix applications. Hydrophobing agents reduce the water Twin range produces excellent substrate
uptake of mineral substrates, plasters and wetting even on critical substrates and
Slip and flow additives paints. The ability of the substrate to simultaneously suppresses foam forma-
TEGO Glide & Flow breathe (water vapor permeability) is tion, particularly in waterborne formula-
Surface additives improve flow, slip and minimally affected. tions.
scratch resistance of coatings. They also
prevent crater formation and flooding of Rheological additives Anti-graffiti additives
pigments. TEGO ViscoPlus TEGO Protect
Rheological additives adjust the viscosity TEGO Protect provides anti-graffiti and
Substrate wetting additives of paints and coatings in a targeted man- easy-to-clean properties in 2-pack poly-
TEGO Wet ner. The TEGO ViscoPlus product line urethane coatings. The TEGO Protect
Substrate wetting additives make possible consists of associative polyurethane thick- range is used as a crosslinkable co-binder
uniform wetting by coatings and printing eners which satisfy the latest require- in solventborne or waterborne, pig-
inks even on low-energy surfaces. This ments of the industry. mented or colorless coatings.

Miscellaneous
ADDID
This product line includes silane adhesion
promoters and polybutadienes. Silane
adhesion promoters form a permanent
chemical link between the coating and
substrate leading to a marked improve-
ment in adhesion. Polybutadienes are
used both to reduce viscosity and achieve
faster drying of offset printing inks.

Hammer effect additives


TEGO Hammer
Additive for producing a hammer effect
finish. The strength of the hammer effect
can be changed by adjusting the amount.

page 48 Technical Background_TEGO Product Groups


Co-Binders Specialty Binders Nanoresins
Synthetic resins Silicone resins Silica-nanocomposites
TEGO VariPlus SILIKOPHEN NANOCRYL, NANOPOX and
TEGO VariPlus resins are non-film-form- The SILIKOPHEN range is based on NANOPOL
ing co-binders based on modified ketone- methyl-phenyl silicone resins. Depending Silica-nanocomposites are preferred
aldehyde resins. These special resins on the formulation, it offers corrosion where high scratch and abrasion resis-
allow targeted adjustment of the proper- protection up to 650C and is used, for tance is needed at the same time as trans-
ties of paints, coatings, printing inks and example, in car exhaust systems or com- parency. The NANOCRYL range consists
other inks. TEGO VariPlus resins can bustion chambers. SILIKOPHEN P resins of silica-nanocomposites in different com-
raise the solids content in paints, the can be cold mixed with organic binders mon UV-curable acrylate monomers.
hardness of coatings and the color (alkyd or acrylic) and are suitable for They are intended for use in radically
strength of pigmented systems. manufacturing coatings with a variety of cured UV paints. NANOPOX materials
properties are based on epoxide resins and corre-
Adhesive resins sponding reactive thinners. The
TEGO AddBond Silicone polyester resins NANOPOL range can be used in sol-
The TEGO AddBond range consists of SILIKOFTAL ventborne products and is almost univer-
powerful adhesion-promoting compo- SILIKOFTAL resins are suitable for heat sally applicable. In spite of the high
nents for paints and printing inks. Adhe- resistant coatings with long-term heat degree of filling (50% silica nanoparti-
sion is promoted on a wide variety of sub- resistance up to 250C. This product cles), they remain crystal clear.
strates. The TEGO AddBond range group combines the properties of the sili-
includes polyester resins for use both in cone resin with those of the polyester and
solventborne, waterborne or radiation- is therefore particularly suitable for deco-
curing paints and printing inks. rative coatings such as cookware, bake-
ware, electrical household appliances and
industrial equipment.

Silicone epoxy resins


SILIKOPON
SILIKOPON resins are the basis for
isocyanate-free, air drying, 2-pack, anti-
corrosion coatings. Coatings made from
SILIKOPON are strongly resistant to
chemicals and have a high color stability
while retaining excellent gloss.

Technical Background_TEGO Product Groups page 49


Defoamers
TEGO Foamex
Foam is a phenomenon which frequently
occurs during the manufacture and appli-
mechanical introduction of air during
applications such as rolling, spraying,
What is foam?
cation of coatings and printing inks. The printing
formation of foam interrupts, for exam- displacement of air when coating A stable dispersion of gas in a liquid is
ple, production processes, reduces the porous substrates called foam. If a stream of air is intro-
effective volumes in the production plant chemical reaction such as the secondary duced into a liquid, the bubbles produced
and leads to unnecessary downtimes. reaction of isocyanates with water assume a spherical shape. Since they are
Foam also interferes with the application lighter than the liquid, the bubbles rise.
process. In printing, foam can cause the Stabilization of the liberated air to form A gas bubble, which has penetrated a sur-
ink reservoirs to overflow and impairs ink foam occurs as a result of surface-active factant-free liquid, has only limited stabil-
transfer from the printing cylinder to the substances (surfactants) present in coat- ity and bursts spontaneously. Air from the
substrate. Dried foam leaves surface ings and printing ink formulations where bubbles escapes and the liquid previously
defects in the paint film. they are essential for stabilizing, dispers- surrounding the air flows back. There-
ing and wetting the formulation. fore, stable foam does not form in pure,
The cause of foam is the introduction of surfactant-free liquids (fig. 1).
gas into the liquid material. The occurrence of foam must therefore
be considered as an undesirable but In liquids such as paints containing surfac-
This can occur by: unavoidable phenomenon in coatings tants, the gas bubbles are stabilized by the
mechanical introduction of air during and printing inks. To prevent foam and surfactants. A surfactant film forms
manufacture by stirring and mixing destroy any foam present, defoamers around the gas bubble. If these bubbles
displacement of air during wetting of have to be added to the formulation. reach the surface, which is also coated
pigments and fillers with surfactants, a surfactant-stabilized
double layer or duplex film is formed
(fig. 2).

macro-foam

micro-foam

Figure 1: Rise and bursting of air bubbles in surfactant-free liquids Figure 2: Rise and stabilization of air bubbles in a liquid containing surfactant

Technical Background_Defoamers page 51


Once the macro-foam bubbles have
penetrated the surface, they initially
become spherical. In this phase, the vol-
gas liquid gas
~10... 100nm ume of the liquid in the foam is greater
than the volume of the air in the foam
foam lamella

macro-foam bubbles. Therefore, this foam is termed


wet foam. The foam bubbles are still
defoamer foam lamella spherical and are stabilized by thick foam
lamellas. The bubbles from the liquid
cause a continuous rise in the foam head.
amphiphilic molecule
The liquid flows out of the foam lamella
gas liquid hydrophobic under gravity. During this so-called drain-
deaerator hydrophilic age process, the proportion of air in the
micro-foam foam increases. The spherical foam is now
forced to take on a more stable polyhedral
water with foam stabilising interfacial region ~ 1nm shape. The polyhedral foam is termed dry
substances
foam because the volume content of
liquid is small. Polyhedral foam consists
Figure 3: Structure of foam and stabilization of the lamella by surfactants
of very thin (approx. 100 nm) but very
elastic foam lamellas, which are stabilized
by the surfactant molecules coating the
surface. The varying structure of foam is
Duplex films can occasionally be fractions summarized in fig. 3.
of a millimeter thick. Despite their very
small film thickness, they can form very
stable foams which are extremely difficult
to destroy. Foam stabilization
One can distinguish between two types Drainage would be expected to com-
of foam: macro- and micro-foam. Macro- pletely remove the water from foam
foam is the foam visible on the surface. lamellas which would then collapse on
Foam bubbles generally have a diameter their own accord. In practice, drainage
of more than 50 m and are stabilized by comes to a halt when loss of liquid in the
a duplex film. Very fine foam bubbles, lamellas causes the surfactant concentra-
which are entrapped in the matrix of the tion to be so high that steric or electro-
coating film, are called micro-foam. To static repulsion forces between the sur-
eliminate macro-foam, defoamers are factant molecules prevent further
used; to eliminate micro-foam, deaerators retraction of the lamella walls. The foam
are used. (see Technical Background lamella attains a thermodynamically stable
Deaerators). state of equilibrium between drainage and

page 52 Technical Background_Defoamers


surfactant repulsion. Highly thinned foam deduce the requirements a compound or As already described, defoamers work
lamellas are therefore very stable and very formulation must meet to be effective as by penetrating and destroying the foam
elastic. The elasticity of the lamellas can be a defoamer. lamellas. It is a prerequisite that the
explained in terms of the Gibbs-Marangoni defoamer is in a position to penetrate the
elasticity. An increase in the lamella surface Requirements for defoamers: surface of the foam lamella. The first
caused by deformation of the foam lamella insoluble in the formulation to be barrier to be overcome when penetrating
leads to a locally reduced concentration of defoamed is the pseudoemulsion film. This is a
surfactant and, with it, an increase in the low surface tension thin liquid lamella between the rising
surface tension of the lamella. The resul- positive penetration coefficient (E) defoamer droplet and the liquid surface.
tant imbalance results in strong restoring positive spreading coefficient (S) or If the pseudoemulsion film is too stable, a
forces towards the energetically more positive bridging coefficient and defoamer droplet cannot penetrate the
favorable unstretched state of the foam dewetting characteristics surface and defoaming is not possible.
lamella (fig. 4).
Fundamentally, a defoamer must be insol- Once the defoamer droplet has overcome
uble in the formulation to be defoamed the pseudoemulsion film and penetrated

How do defoamers where it should be present in the form of


finely divided droplets. Furthermore, it is
the lamella, its further behavior can be
described using the penetration coeffi-
work? necessary for it to be sufficiently compati- cient which can be calculated from the
ble with the medium to be defoamed not interfacial tensions between the three
Whether defoamers or deaerators are to cause surface defects such as craters. phases: the liquid to be defoamed,
used depends on the type of foam, i.e The choice of defoamer is therefore always defoamer and air. It describes the force
macro- or micro-foam. To eliminate a compromise between defoaming perfor- equilibrium between the three phases.
macro-foam on the surface, prevent large mance and compatibility/insolubility.
air occlusions and for rapid foam collapse
in waterborne formulations, defoamers
are preferred. If finely dispersed air needs
to be removed from the system, deaerators
are preferred. In practice, it is usually not
possible to differentiate clearly between
defoamers and deaerators. Most defoam-
ers are also effective to some degree as Figure 4: Gibbs-Marangoni elasticity

deaerators and the reverse is true. The with surfactants to saturated interface
region to lower surface tension
mechanisms of deaeration are described Gibbs-Marangoni elasticity
in the section on deaerators.

Defoamers work by penetrating the foam


lamella, destabilizing it and making it
burst. Investigations using model systems retraction
have resulted in various mechanisms of
defoaming being discussed in the litera- elongation
ture. From the models, it is possible to

readjust power to equilibrate


surface tension

with surfactants to un-saturated interface


region to increased surface tension

Technical Background_Defoamers page 53


Only if the penetration coefficient
remains positive, does the defoamer S =gw/agw/ogo/a = gw/a(gw/o+go/a)
remain permanently on the lamella
spreading coefficients formula
surface. If the penetration coefficient is
negative, the defoamer drop can migrate
back to the liquid phase.

are impaired and it may collapse. The Defoamers with insufficient spreading
E =gw/a+gw/ogo/a spreading process leads to flow of the power may defoam through another
lamella liquid along the direction of mechanism called bridging. The basic
gw/a= surface tension of the foaming spreading. This phenomenon, also known prerequisite is that the defoamer is
liquid as Marangoni flow, causes a local thinning capable of penetrating the foam lamella
gw/o= interfacial tension between of the lamella at the location of the and has a positive penetration coefficient.
the defoamer and the foaming spreading defoamer droplet and leads to Defoaming by bridging requires that a
liquid further destabilization of the lamella. The defoamer droplet which has penetrated
go/a= surface tension of the defoamer penetration and spreading of a defoamer the lamella surface must also be capable
droplet is illustrated in fig. 5. of penetrating the opposite lamella side.
Frequently, this is only possible once
The spreading behavior can be described the lamella has been sufficiently thinned
If one assumes the interfacial tension of via the spreading coefficients as the equi- by continued drainage. In some cases,
the foaming medium gw/a is constant, the librium of the surface tensions of the defoamer droplets become sufficiently
equation shows that a positive spreading three phases with each other. Only large by coalescing with other defoamer
coefficient can only be achieved if the defoamer droplets with positive spreading droplets for the bridging mechanism to
surface tension of the defoamer go/a is coefficients can spread on the surface of occur. If the defoamer droplet has pene-
sufficiently small. the medium to be defoamed. trated both sides of the lamella, a subse-
quent dewetting or stretching mechanism
The defoamer droplet may spread after The equation for spreading coefficients can lead to rupture of the lamella.
penetrating the lamella. If a defoamer can shows that defoamers can only spread
spread on the surface, it forms a defoamer if the sum of their interfacial tensions to
lens at the lamella surface and displaces air and to the medium to be defoamed is
the surfactants at this location. As a result, smaller than the surface tension of the
the stability and flexibility of the lamella foaming liquid.

Figure 5: Penetration and spreading of the active ingredient of the defoamer

page 54 Technical Background_Defoamers


B =(gw/a)2+(gw/o)2(go/a)2
bridging coefficients formula

A basic condition for both mechanisms is If defoaming takes place via a stretching
for the bridging coefficient of the mechanism, the bridging defoamer drop-
defoamer to be positive. let marks the weakest point in the lamella.
If the lamella stretches, it ruptures at even
Calculation of the bridging coefficients very low stretching forces on the
involves the square of the interfacial ten- defoamer droplet (fig. 7).
sions. The bridging coefficient can only
be positive if the interfacial tension
between the defoamer and air is suffi-
ciently small.

In the case of the dewetting mechanism,


the foaming liquid is not capable of wet-
ting the surface of the defoamer droplet.
Consequently, dewetting of the defoamer
droplet occurs and the foam bubble col-
lapses. Solid defoaming agents can also
Figure 6: Film bridging during defoaming
act via a dewetting mechanism (fig. 6).

Figure 7: Dewetting during defoaming

Technical Background_Defoamers page 55


individual coatings formulations. Polysi-
loxane defoamers have very high spread-
ing characteristics and are highly effec-
tive. They are used particularly frequently
in modern waterborne coatings and print-
ing inks where high demands are made
on defoaming characteristics and surface
finish. Applications include pigmented
and unpigmented wood, architectural and
industrial coatings and printing inks. They
do not impair gloss and are distinguished
by good compatibility. Modified poly
siloxanes are synthesized by forming a

Which classes of substance have a Si-O-C or a Si-C link between the


siloxane block and the organic modi
defoaming effect in waterborne coatings? fication (fig. 8).

Typical active substances for formulating Silicone defoamers (polysiloxanes) Mineral oil defoamers
defoamers for waterborne coatings are:
polysiloxanes (silicones), mineral-, vege- Polysiloxanes and modified polysiloxanes Mineral oils, with their high spreading
table-oils and/or polymers. Particularly belong to the most widely used group of power and high incompatibility, have long
effective defoamers tailored to specific defoaming substances. An enormous been used as defoaming agents. Nowa-
applications can be formulated by com- range of defoaming agents is accessible days, aliphatic mineral oils are used in
bining the substances with each other and via modification with polyethers or other defoamer formulations. Aromatic oils are
also by adding fine-particle hydrophobic polymers. The compatibility and effec- increasingly rare because of environmen-
solids such as silicas. tiveness of these can be adjusted to suit tal and physiological considerations. Min-
eral oils are frequently used in the archi-
tectural paints and printing inks sectors.
When used in waterborne formulations,
where high demands are made on the
Figure 8: Typical polyether siloxane structures gloss of the finish, mineral oils frequently
ABA block copolymer comb-shaped copolymer reach their limits since they tend to impair
ABA block copolymer comb-shaped copolymer
gloss or cause other surface defects.

branched
copolymer branched
copolymer
A(BA)n block copolymer

A(BA)n block copolymer


n-1

n-1

Me
Si O and similar hydrophobic polyether
Me

Me
Si O and similar hydrophobic polyether
Polyether polysiloxane copolymer structures Me

Polyether polysiloxane copolymer structures


page 56 Technical Background_Defoamers
Vegetable oil-based defoamers
How are defoamers incorporated?
As renewable raw materials, vegetable
oils are increasingly important in the for- Choosing the method of incorporating a defoamer emulsions, the defoamer drop-
mulation of defoamers. They exhibit high defoamer is largely dependent on the lets which provide the defoaming effect
incompatibility and have very similar form in which it is supplied. Common in the finished coatings formulation must
properties to those of mineral oils. They forms are defoamer emulsions or concen- first be generated. This is typically done
are used mainly in architectural paints but trates. during incorporation of the concentrate
are increasingly important in other sec- by finely dispersing the defoamer in the
tors. In defoamer emulsions, the active sub- coating using sufficiently high shear
stance is already finely distributed in an forces. It is therefore recommended that
emulsified form. Defoamer emulsions can the defoamer concentrate be added to the
Polymer-based defoamers therefore be incorporated in the formula- millbase. The incorporation conditions
tion using low stirring intensity. They are can directly influence the effectiveness of
Examples of polymer-based defoamers also suitable for subsequent addition in the defoamer. Dispersing which is too
include modified fatty acids, polyethers the ready-to-use formulation. Typical weak results in defoamer droplets which
or modified amides. The polarity of the examples of Evoniks defoamer emulsions are too large and causes surface defects.
defoamers can be adjusted via the com- for waterborne coatings and printing inks If the defoamer is too strongly dispersed,
position of the polymers. The effective- are TEGO Foamex 805 N, 815 N, 822, the defoamer droplets are too small and
ness of polymeric defoamers is frequently 825 or 1488. cannot develop their full effectiveness
inferior to that of other substances. (fig. 9). Defoamer concentrates from the
However, the wide choice of polymeric Defoamer concentrates consist mainly of TEGO product range are TEGO Foamex
defoamers enables the effectiveness and the active defoamer substance. They are 3062, 810, 883 and 8050.
compatibility of the defoamer to be pre- water- and solvent-free. In contrast to
cisely adjusted for very critical coatings
systems. Therefore, polymeric defoamers
are frequently used in formulations
where other defoamer technologies are
too incompatible.
Figure 9: Effectiveness as a function of droplet size

compatible optimum incompatible


good
defoaming efficiency

defoamer/
deaerator
bad

droplet size of defoamer

Technical Background_Defoamers page 57


Which tests are recommended for evaluating defoamers?

Decisive criteria for choosing a defoamer ing characteristics are strongly influenced olume of a control sample without
v
are the formulation and application by the conditions during manufacturing defoamer is checked before and after
method. Different formulations require and application of the paint, it is recom- the stir test.
different defoamers. Important parame- mended that the test method permits
ters affecting the formulation include pig- evaluation under conditions close to
ment loading or the chemical nature of those in practice. The method should Flow test
the binder. The type of application also include an assessment of possible
method also affects the incorporation of surface defects that could be caused by In this test, air is stirred into the formula-
foam in the coating material and thus the the defoamer. tion with a fast running stirrer. The freshly
choice of defoamer. Defoamer recom- foamed sample is poured onto a surface.
mendations from Evonik take into account The activity of the defoamer can be
suitability for particular formulations and Stir tests assessed from the fresh pour-down. After
application methods. Nevertheless, it is the pour-down dries, the film can be visu-
recommended that defoamers are tested A frequently used method for low to ally assessed for foam and surface defects.
in the laboratory before using them in medium viscosity formulations is the stir The flow test frequently complements the
production. test in which air is stirred into the formu- stir test and is similarly suitable for low to
lation with a fast running stirrer. The medium viscosity paints.
When choosing a defoamer for a formula- effectiveness of different defoamers can
tion, its effectiveness should first be be compared via the volume of foamed
checked in the laboratory. Since defoam- material. It is recommended that the

page 58 Technical Background_Defoamers


Roller test

The roller test is used for testing paints


which are applied with rollers and simu-
lates real application conditions. The paint
is applied with a roller to a substrate and
foaming during application is assessed.
Surface defects caused by foam, incom-
patibilities or air occlusions in the coating
can be assessed on the dried paint film.

All procedures are shown in videos on our


homepage.

FAQs:
We use TEGO Foamex 810 in a pig- indirectly via other raw materials for What types of pumps are suitable for
mented UV wood finish and sometimes which the defoamer is suited. Therefore, conveying defoamer emulsions?
have isolated craters on the application there cannot be a universal defoamer Defoamer emulsions should, in principle,
unit. Unfortunately, we cannot repro- which always functions in all formula- be conveyed with low-shear pumps.
duce this defect in the laboratory. What tions. However, empirical experience has Continuous stirring or pumping should
can we do? shown that certain defoamers are well be avoided as this can cause changes in or
One way of eliminating craters is by add- suited for individual areas of application. destabilization of the defoamer emulsion.
ing a wetting agent such as TEGO Wet TEGO Foamex 1488 or TEGO Foamex
270 or TEGO Twin 4100 in amounts of 855 or TEGO Foamex K 8, for example,
0.1% to 0.4%. perform well over a wide spectrum in the
PVC range between 50 to 80% and in
We manufacture various interior paints. typical binders for this range of PVC
The PVC ranges from 50% to 80%. We such as styrene acrylic or vinyl acetate
also use various binders in these paints. copolymers.
At the moment, we are also using a vari-
ety of defoamers. Is there a defoamer Can defoamer emulsions be diluted with
which is effective in all paints? glycols to mix the defoamer into coatings
Foam formation and stabilization are without compatibility problems?
usually caused by a mix of emulsifiers and We basically recommend adding
stabilizers from the binder and other sur- defoamer emulsions in the form supplied.
face active substances added directly or Diluting with solvents can destabilize the
emulsion and cause it to break.

Technical Background_Defoamers page 59


Deaerators
TEGO Airex
Figure 1: Surfactants orient
themselves at the liquid/air
interface

Foam a well-known problem

Foam is one of the most common prob- Not all foams are the same orient themselves in this interface and
lems which a formulator must consider encapsulate the micro-foam bubble
when developing coatings and printing There are two types of foam: micro-foam (fig. 1).
inks. It is particularly important in water- and macro-foam. However, it is fre-
borne, radiation-curing, solvent-free and quently difficult to distinguish easily The TEGO Foamex range of coatings
high solids formulations. between these foam types as they often additives from Evonik eliminates primarily
occur together as a foam problem. macro-foam particularly in waterborne
Foam is a stable distribution of small gas formulations. However, depending on the
(usually air) bubbles in a liquid. Pure liq- In principle, it is possible to classify structure of the additive, they are also
uids, however, do not foam. A stable macro- and micro-foam. The former is effective against micro-foam. These prod-
foam can only occur when substances found in, for example, the coating film ucts are fully described in the Technical
with a surfactant structure are present in surface, the latter is found within the Background Defoamers.
the liquid. coating film. Both types of foam can be
distinguished in the liquid coatings mate- TEGO Airex additives are predominantly
Surfactants, with their hydrophilic and rial and in the dried/cured coating film. effective against micro-foam although
hydrophobic regions, orient themselves they show positive effects when tackling
preferentially at the liquid/air interfaces. Macro-foam bubbles in liquid paint are macro-foam. The mode of operation of
A liquid with included or incorporated air generally air bubbles surrounded by a the TEGO Airex family is described
has such interfaces. Surfactants orient duplex film of a surfactant double layer. below.
themselves at this interface and thus sta- Two liquid/air interfaces exist here.
bilize the air bubbles producing stable Micro-foam bubbles can be described as
foam. air inclusions which only exhibit one
liquid/air interface. The surfactants also

Technical Background_Deaerators page 61


Figure 2: Waterborne wood coating, airless application

Micro-foam is usually only recognized


at second glance

Many coating problems are not thought How is micro-foam formed?


of as being associated directly with micro-
foam. Furthermore, entrapped air is often Micro-foam consists of small air or gas
only recognized with the help of visual bubbles in the coating. When present,
aids such as a magnifying glass or micro- surfactants orient themselves at the air/
scope. liquid interface, i.e. the air or gas bubble,
and stabilize it (fig. 1).
Turbidity effects or a reduction in gloss in
a coating can be caused by micro-foam Air or gas can be incorporated in the coat-
bubbles, an undesirable effect in, for ing film by:
example, high gloss finishes (fig. 2). stirring/mixing/dispersing during
manufacture of the coating
Premature corrosion can be caused by mixing when adding curing agents in
micro-foam bubbles since they reduce the 2-pack systems
effective film thickness of the coating. application processes such as rolling,
Micro-foam bubbles can also cause small dipping, spraying and, most impor-
pinholes as the coating dries. These are tantly, airless-/airmix-spraying
small channels which can reach right release of gas by chemicaI processes
down to the metallic substrate. The pro- during curing of the coating (e.g.
tective function of the coating is compro- release of CO2 through reaction of iso-
mised and corrosion can progress more cyanate with moisture)
rapidly. application on porous substrates such
as wood or stone (air entrapped in
pores rises in the coating)

page 62 Technical Background_Deaerators


Besides the surfactants, two further fac- This means that if the coating viscosity Fig. 4 shows the rising velocity of an air/
tors play a key role in the formation of is relatively high, the rate of rise of the gas bubble at constant velocity as a func-
micro-foam: air/gas bubble is relatively small. Air/gas tion of its radius, i.e. its size based on
the viscosity of the coating bubbles, particularly in formulations with Stokes Law.
the size of the air or gas bubbles a relatively high viscosity (e.g. high solids
or UV formulations, floor coatings, high The rising velocity of very large air/gas
build glazes, anti-corrosion coatings), bubbles increases exponentially. These
Micro-foam relationship between rise slowly to the coating surface. The reach the surface during curing or drying
viscosity of the coating and the bubble viscosity of the coating increases as dry- of the coating where they form macro-
size ing/curing progresses. As a consequence, foam and can be eliminated with the aid
the bubbles remain in the coating film of defoamers (see Technical Background
The factors mentioned are closely related and result in the well-known problem of Defoamers).
by Stokes Law which, in simplified form, is: micro-foam.
This raises the question: What happens
v ~ r / 2 However another important relationship
is indicated by Stokes Law: the size of
with small air/gas bubbles, known as the
micro-foam? An answer is given in the
the air bubble has a far more marked next section.
where effect on the rising velocity than the vis-
v = velocity of rise of the foam bubble cosity of the coating because the radius of
r = radius of the foam bubble the bubble appears to the power of 2 in
= viscosity of the coating the equation.
(fig. 3).

Figure 3: Rising speed depends on viscosity of the paint and size of the bubble Figure 4: Rising speed depending on the radius of the bubble
rising speed (v)

V Rising speed

foam bubble radius (r)

Technical Background_Deaerators page 63


Figure 5: View through a micro-
scope: dissolving of micro-bubbles
with time lapse, waterborne on
glass, airless application
Micro-foam immediately after application Micro-foam after 10 min Micro-foam after 20 min

Can micro-foam bubbles dissolve of At first, there is a mixture of micro-bub- equation, which relates the internal pres-
their own accord? bles of different sizes. As drying pro- sure of a micro-foam bubble to the exter-
ceeds, the picture alters. Relatively nal pressure of the surrounding medium.
Micro-foam bubbles can disappear of large micro-bubbles slowly become The smaller the micro-foam bubble, the
their own accord. They continuously larger while small micro-bubbles rapidly greater the rise in the internal pressure
shrink until they disappear. This phenom- become even smaller. They literally compared to the external pressure. This
enon can be easily observed using a shrink until they disappear. pressure difference causes air from the
microscope during, for example, the dry- micro-bubble to diffuse into the sur-
ing phase of an airless-applied coating. The driving force for the shrinkage of the rounding medium and dissolve there.
One can easily track how the micro-foam small micro-bubbles is the Laplace pres- Diffusion, and with it, shrinking of the
bubbles change during this time (fig. 5). sure of the foam bubble. The Laplace micro-foam bubble continues faster and
pressure is given by the Young-Laplace faster as the bubble becomes smaller.

Young-Laplace equation
How do deaerators
work?
Effective deaerators exhibit a partial or
targeted insolubility in the medium to be
treated and, ideally, a certain surface
activity. The deaerators concentrate pref-
interfacial
tension erentially at the liquid/air interface and
form, in the ideal case, an additive film
The internal pressure of an air bubble is Laplace Pressure around the micro-foam bubble. They thus
greater than the external pressure as the Derived from the Young-Laplace prevent stabilization of the bubble by sur-
effect of interfacial tension must be over- equation with Pi = Pa + 2s/r. factants. In addition, the partially insolu-
come. The ratio of the interfacial tension Pi = internal pressure of air bubble ble active deaerating substances promote
to the radius of the bubble 2s/r is greater Pa = external pressure of air bubble diffusion of air from the micro-foam bub-
the smaller the air bubble. This leads to an s = interfacial tension ble into the surrounding medium.
increase in the internal pressure Pi. For r = radius of the air bubble
small air bubbles between 10 and 20 m
diameter, the internal pressure can be 10
to 15% higher than the external pressure.

page 64 Technical Background_Deaerators


Partial or targeted incompatibility of the
deaerator means that there is an optimum
balance between the effectiveness of the
deaerator and the coatings formulation.
On the one hand, if the deaerator is too
compatible it would not be effective. On
the other hand, if it is too incompatible,
defects such as craters, fish-eyes or tur- Figure 6: Solventborne clearcoat with different deaerators added: from left to right, completely soluble/
bidity would occur (fig 6). insoluble/partially or targeted insoluble/incompatible

What substances are effective Is there a universal deaerator? Combinations of additives are helpful
deaerators?
A deaerator is effective against micro- In cases where deaerators are highly
There is a wide range of chemical com- foam and, at the same time, sufficiently effective but cause surface defects such
pounds which are potentially suitable for compatible with the paint, lacquer or as craters, a combination with substrate
use as deaerators in coatings including: printing ink formulation. This means that wetting agents or surface active additives
organic polymers such as polyethers or the deaerator prevents/eliminates micro- is recommended (see Technical Back-
polyacrylates foam but does not give rise to, for exam- ground Slip, Flow and Radiation-curing
dimethylpolysiloxanes (silicone oils) ple, flow problems, fisheyes, craters or Additives, and Substrate Wetting Addi-
organically modified polysiloxanes, turbidity. tives).
such as aryl-alkyl modified polysiloxanes
fluorosilicones This balance is dependent on the coating
formulation. Changes, particularly in Storage stability tests are necessary
These are frequently used for formulating binder or solvent, strongly influence
deaerators. Such deaerators are supplied the effectiveness and compatibility of a High storage stability is expected from
in the following variants: deaerator. Therefore, there is no universal many coatings systems. The ideal deaera-
as concentrates with 100% active deaerator for all coatings systems. Rather, tor should therefore be effective and
ingredient content not only the effectiveness but also the compatible even after extended storage.
as solutions in organic solvents compatibility of the deaerator with the Tests under specified conditions are
as aqueous emulsions, specially for coatings system must be checked. The essential (e.g. four weeks at room tem-
use in waterborne formulations choice and amount of deaerator used in perature, 40C and 4C). In many cases
the formulation as well as the method a combination of several deaerators or a
The effect of deaerator formulations is of application play important roles. Pre- deaerator and defoamer is the best
further enhanced by the addition of liminary tests are certainly helpful in choice.
hydrophobic solids to the above men- choosing possible deaerators.
tioned active substances. Hydrophobic
solids used include silicas, ureas or metal- It is essential to confirm the choice of
lic soaps. deaerators by evaluation under end-appli-
cation conditions.

Technical Background_Deaerators page 65


Which test methods for preliminary selection of deaerators
have proven themselves?

Test method for low to medium visco- application. After drying/curing, the In the case of high-build application, the
sity coatings formulations micro bubble is examined using a magni- freshly foamed coatings material can sim-
fying glass or microscope. It can be help- ply be filled into a lid (e.g. of a metal
50 g of the coating is stirred for 1 minute ful to document the results using photos. paint can or poly beaker) and taken out
at a high speed (3,000 rpm) on a dis- for assessment after curing (see also video
solver with a disc. This causes air to be Evaluation of pigmented coatings can Deaerating of floor coatings)
incorporated and finely distributed in the often be difficult because of their poor
coating. Immediately after stirring, the transparency. In this case, differences in
coating is poured down on a transparent gloss can be used as a criteria: the more Testing of the finest micro-foam
polyester film fixed on a glass panel micro bubbles, the lower the gloss.
inclined at 25 to the perpendicular. Micro-foam can occur in such a fine form
During drying, the coating can deaerate. that it is not visible to the unaided eye and
After drying, the film is assessed visually Testing of high viscosity coatings com- examination through a microscope or
for bubbles, pinholes (effectiveness) and pounds magnifying glass, etc., is required. How-
for possible defects such as craters, fish- ever, there are other methods of render-
eyes, turbidity or flow problems (compat- For coating compounds (e.g. 2-pack floor ing visible or measuring the very fine
ibility) (fig. 7). coatings) the flow test on inclined sur- pores which can result from micro-foam
faces is unsuitable. For such formulations, bubbles in the coating:
casting of defined film thicknesses (e.g. 3
Test method for medium to high visco- mm) has proved satisfactory. In this test,
sity coatings formulations the coating material is sheared for 2 min- Copper sulphate test
utes at 2,000 rpm to incorporate air.
It is difficult to find the ideal deaerator Directly afterwards, the material is The coating is applied in a realistic thick-
by means of simple preliminary tests, poured onto a PE film. After 10 minutes, ness to a sand-blasted steel panel. After
particularly for formulations applied in one third of the surface is screeded and, completely drying or curing, about 4 ml
thick layers by airless/airmix methods. after drying/curing, visually assessed for of 10% copper sulphate solution is
It is more meaningful to carry out a spray foam bubbles or surface defects. (fig. 8) poured into a small watch glass. The
panel is placed coated-surface down on
the filled watch glass and the apparatus
inverted so that the copper sulphate solu-
tion can react. After 24 hours, the coating
Figure 7: Test foil from the flowout test, left with deaerator, right without additives surface is rinsed with water. If there are
fine pores in the coating, they show up as
red dots. These red marks are elemental
copper deposited from the copper
sulphate solution while iron has been
dissolved from the panel.

page 66 Technical Background_Deaerators


Pinhole detector

This method is based on the fact that all


electrically insulating coatings materials
have a higher dielectric strength than air.
Pores are detected by arcing between the
test electrode and conductive substrate
where there is a defect. The presence of
pores is shown optically and acoustically.
However, the detector can only be used
for coatings on conductive substrates.
Figure 8: Specimen of a floor coating

Assessment of entrapped air in coatings


for wooden frames or panels

This method is used to assess entrapped How important is the method of applica- should be engineered to minimize the
air in coating films (after drying/curing) tion when choosing the deaerator? entrapment of air in the coatings material.
which are applied to wood substrates. The method by which the coating is However, parameters such as raw materi-
Defined cross-sections of the coating applied plays a very important role. There als, manufacturing regulations and appli-
film/wood substrate are produced and are deaerators which, because of their cation are usually specified and the room
examined microscopically to assess the strong incompatibility produce, for exam- for maneuver is thus significantly
number and size of micro-foam bubbles. ple, a break of curtain at the curtain restricted. The addition of coatings addi-
This method is particularly well suited for coater machine. In this case, only rela- tives is the simplest way of preventing and
pigmented formulations. tively compatible deaerators should be eliminating micro-foam.
used.

With airless and airmix application, micro-


FAQ: bubble formation is very strong. This
requires especially effective and, there-
At what stage in a coatings formulation fore, more incompatible deaerators and a
should the deaerator be added? good balance between effectiveness and
Deaerators can be added to the millbase compatibility must be found.
or the let-down. This depends primarily
on the incompatibility of the deaerator What fundamental ways are there of
with the coating system. It is generally preventing micro-foam?
true that the greater the incompatibility, There are various possibilities of counter-
the more shear force is required. Some acting micro-foam in coatings and print-
deaerators are excellent as millbase ing inks. The choice of low-foam raw
deaerators while others can be used in the materials or optimally adjusting the coat-
let-down or in clear coats. For the ideal ing viscosity can significantly reduce
point of addition, please see the product micro-foam problems in a formulation.
data sheets. Production and application of the coating

Technical Background_Deaerators page 67


Slip and Flow Additives
Radiation-Curing Additives
TEGO Glide TEGO Flow TEGO Rad
The customer's wish: the perfect finish

Diverse demands are made on paints and they improve substrate wetting, promote
varnishes. On the one hand, the require- flow and impart slip. Thus slip and flow
ment is for brilliant, smooth coatings. On additives significantly reduce the suscepti-
the other hand, the desire is for func- bility to defects, resulting in a high-qual-
tional, continuous coating films which ity appearance and markedly improved
ensure chemical and mechanical resis- scratch resistance, especially with freshly
tance, adequate slip, haptic properties and applied coatings.
also a certain antiblocking/release effect.

A coating has a large interfacial area for Eliminating unevenness:


its volume. There are actually two inter- flow or leveling
faces, one with the substrate and another
with the surrounding air. Slip and flow The term "leveling" indicates the
additives are active at these interfaces intrinsic property of coatings to even
where, depending on their structure, out imperfections which arise from spray
mist, brush strokes, etc. (DIN 55945).

Figure 1: Defect-free surface


The leveling of a coating material is
strongly dependent on its flow properties,
surface tension, application parameters
and drying conditions. If the flow is
inadequate, surface defects such as
pronounced texture, voids and craters
in the coating surface occur. In contrast,
coatings with good flow, when applied
on a suitable substrate, produce smooth
surfaces of exceptional optical brilliance.

Technical Background_Slip and Flow Additives_Radiation-curing Additives page 69


Producing a uniform surface tension:
low surface tension high surface tension
polyethersiloxanes

Polyethersiloxane-based additives adjust


the surface tension of drying coatings to
a uniform, low level and thereby even out
differences in surface tension. This mini-
mizes flow of material from regions of
low surface tension to regions of high
surface tension and thus suppresses eddy
formation. The solvent evaporates evenly
Figure 2: Bnard cells
from the whole surface so that the film
dries very homogeneously and shows
much better leveling.

Bnard cells: differences in surface


tension Orientation of matting agents

To achieve good flow, the surface tension rying layer, a phenomenon known as
d Bnard cells are a particular problem in
must remain uniform over the complete the formation of Bnard cells. The surface mixed-pigment formulations. The differ-
surface of the coating layer while it is tension is higher at the edges of the cells ent particle sizes and densities of the vari-
drying. During the drying of a solvent- than at their centers and coating material ous pigments lead to separation of the
borne coating film, the solvent on the flows from regions of lower surface ten- previously homogeneously distributed
surface evaporates causing differences in sion to regions of higher surface tension. pigments. In the resulting eddies, pig-
temperature, surface tension, solvent The resulting unevenness in the surface ments of different densities are dragged
concentration and density within the film. dries into the coating film. This produces along to various extents. Smaller pigment
To balance the thermodynamic non-equi- an irregular surface as the coating shows particles are transported further than
librium, currents occur in the coating film. marked texture (fig. 3). larger ones and accumulate at the edges
These currents produce eddies in the of the eddies. The different pigments are
partially de-mixed and later a honeycomb
structure appears in the drying film (see
also "Technical Background Wetting and
Figure 3: Surface texture with and without flow additive Dispersing Additives"). In matte clear
coats, the large particles mainly remain in
the center of the cells. A higher degree of
gloss is visible at the edges of the cells than
in the centers. When applied to a vertical
surface the cells become deformed and
streaks become visible (fig. 4).

page 70 Technical Background_Slip and Flow Additives_Radiation-curing Additives


These effects are also suppressed by addi-
tives based on organo-modified siloxanes.
Exactly as in the improvement of leveling,
the effect is due to an equalization of the
surface tension. For this reason some
wetting and dispersing additives such as
TEGO Dispers 610 S, contain small
Figure 4: Matte clear-coat without additive (left) and with modified siloxane (right)
amounts of modified siloxanes in addition
to their actual active agent.

Exceptionally good overcoatability:


polyacrylates

Unlike polyethersiloxanes, polyacrylates


rarely alter the surface tension. Polyacry-
lates have limited compatibility in the
coating formulation and accumulate at the
interfaces during the drying process. The
viscous acrylate polymers slow down the
Figure 5: Craters which can be eliminated with polysiloxane
process of evaporation. Because of their
high molecular weight between 5,000
and 10,000 g/mol, polyacrylates are rela-
tively immobile at the interface. They act Resistance to slip depends on unevenness can be achieved by slip additives. The
as a barrier to the flow of material caused in the surface of the coating and the body scraping object slips off rather than pene-
by the difference in surface tension so sliding on it as well as the interaction trating into the coating film. Smooth sur-
that texture cannot develop in the surface. between them. Resistance to slip is par- faces exhibit markedly reduced scratch
The surfaces are already very smooth ticularly low if the interactions within a susceptibility.
immediately after the coating is applied lubricating film and between the surfaces
and, as the surface energy of the dried sliding on each other are small. Slip addi- Scratch resistance is improved signifi-
coating is not reduced, the wetting prop- tives are used to ensure particularly slip- cantly only if slip additives are formed
erties of a subsequent layer are not critical. pery surfaces. from segments which interact weakly
with each other. Organo-modified
siloxanes, with a high proportion of
Matte or slippery? Smooth surfaces are not susceptible polydimethylsiloxane segments, exhibit
to scratching particularly weak interactions both with
Some customers want matte surfaces, for each other and with other materials.
example to lower the danger of slipping Scratches are visible as linear damage to This makes them ideal as slip additives.
when used as floor coatings. Other cus- the surface. They arise when a harder Organo-modified siloxanes minimize
tomers want smooth surfaces to increase object scrapes over the coating film and unevenness in the surface and help the
the slip of printed items or packaging. irreversibly distorts or even penetrates coating to form particularly smooth sur-
High-quality furnishings and cars are also the surface. Such damage is markedly faces. During the drying process, the
protected against scratching by more slip- lowered by increased surface slip which organo-modified siloxanes continually
pery surfaces.

Technical Background_Slip and Flow Additives_Radiation-curing Additives page 71


accumulate at the surface. A film is pro- Durable release effects Formulation counts
duced which makes it possible for a solid
body to slide. Hydrodynamic lubrication In contrast to conventional flow and slip During drying or curing of the paint film,
occurs and the slip resistance is signifi- additives, TEGO Rad products can be the solubility of the slip additive in the
cantly reduced. incorporated into radiation-curing formu- film decreases continuously. Therefore, it
lations. Here additives should chemically accumulates at the surface. In general, the
cross-link with the radiation-curing binder efficacy of the additive is significantly
Avoiding craters matrix. Acrylate groups form a network higher in strongly crosslinked formula-
with the binder on radiation-curing and tions than in those which are less cross-
Craters are small depressions in coating this minimizes the tendency of the addi- linked or dry physically.
films, sometimes extending right down to tive to migrate. In this way longer-lasting
the substrate. Their origin can be traced surface effects and sometimes extreme Slip additives are particularly effective in
back to poor wetting by the liquid coating anti-blocking/release effects can be solventborne formulations where they
(see also Technical Background Substrate achieved. Targeted modification allows are transported with the solvent to the
Wetting Additives). Craters are either substrate wetting or deaeration. surface during the drying process. After
formed on low energy substrates such as drying, they ensure a low friction inter-
plastics or occur due to contamination of TEGO Rad products offer, depending on face.
the freshly applied coating. The liquid the structure, different combinations of
coating does not fully wet the contamina- effects. TEGO Rad 2100 combines com- For most physically drying and water-
tion, and this reduces the contact area patibility with flow promoting properties. borne coatings, markedly higher additive
resulting in a crater. Reduction of the sur- TEGO Rad 2010 combines very good concentrations are necessary. This is
face tension by polyethersiloxanes facili- substrate wetting with low surface because there are many more interfaces
tates wetting of a contaminated or an smoothness. Whereas, TEGO Rad 2700 present in emulsions and dispersions to
inadequately cleaned substrate so that exhibits excellent anti-blocking/release which surface active additives orient than
no craters are formed. In extreme cases, and also has a degassing function. is the case in a homogeneous resin solu-
substrate wetting additives, such as spe- Because of the desired incompatibility, tion. Additionally, the surfactants or
cially formulated silicone oils like TEGO products such as TEGO Rad 2700 have emulsifiers interact with the additives.
Flow ATF 2, are recommended as anti- to be incorporated using high shear. Here again their effectiveness in cross-
crater additives. linking formulations is greater than in
those which dry physically.

When the addition is not made in the


Figure 6: Release effect form of a solution, care must be taken to
ensure adequate stirring to incorporate
the additive homogeneously. This applies
particularly to waterborne and radiation-
curing coatings in which the additives
disperse more slowly than they do in
organic solvents.

page 72 Technical Background_Slip and Flow Additives_Radiation-curing Additives


Chemistry of surface active additives

Eliminating the defects described above


depends largely on the surface activity of
the additives. Substances are said to be
surface active if they reduce the surface
Figure 7: UV crosslinked coatings on CDs
tension of a liquid by concentrating at the
interface to form a new but less energetic
boundary surface. Further explanations of
surface tension are given in the Technical
Background Substrate Wetting Additives.

In solventborne formulations, which by


nature exhibit low surface tension, sili-
cone oils and modified siloxanes are sur-
face active.

Modified siloxanes are a particularly ver-


Figure 8: Clear coat with silicone oil (left) and with polyethersiloxane (right)
satile group of substances and are found
in diverse forms in the TEGO range of
products. Modified siloxanes are derived
from low molecular weight polydimethyl-
siloxanes by replacing individual methyl of modified siloxanes depends on the sili- The use of surfactants:
groups with very diverse organic side cone content, the structure of the siloxane improves substrate wetting
chains. These increase compatibility with backbone and the organic side chains. improves flow
binders. The organic side chains are fre- Modified siloxanes are used successfully generates a uniformly textured surface
quently polyethers, or, less commonly, as slip and flow additives. prevents floating of pigments and mat-
long chain alkyl groups. Modified silox- ting agents
anes are considerably more soluble and The crosslinkability of TEGO Rad prod- reduces sliding resistance
binder-compatible than polydimethyl ucts and the durability of their surface improves scratch resistance
siloxanes. effects are based on incorporating reac-
tive acrylic groups in the modified silox- There is no clear delineation between slip
The most important type of modification ane. During radiation-curing the additive and flow additives and their effects are
is with polyethers. As a rule, polyethers is polymerized into the molecule and thus therefore considered together. Usually they
are manufactured from ethylene oxide cannot migrate. This technique achieves are modified polysiloxanes with a wide
and/or propylene oxide. The higher the extreme release effects but overcoatabil- range of molecular weights from 1,000 to
ethylene oxide content, the more hydro- ity and overprintability are impaired. The 15,000 g/mol. To be effective in a given
philic the resulting product is. Even water- mobility of the slip and flow additives is a system, they must be compatible in the sol-
soluble siloxane compounds can be prerequisite for overcoatability and unim- vent (in waterborne formulations, water)
obtained. Basically, the property profile paired adhesion in multicoat finishes. but still develop their surface activity.

Technical Background_Slip and Flow Additives_Radiation-curing Additives page 73


Recommended additives

Non-turbid flow, particularly in clear


coats, is achieved with the highly compa
tible TEGO Flow 370 which is especially
effective in smoothing the surface during
spray application. The same additive pro-
motes flow in coil coatings without stabi-
lizing air. TEGO Glide 410 achieves the
greatest reduction in sliding resistance in
solventborne formulations. The addition
of just 0.1% on the total formulation
Figure 9: Measurement of slip properties (schematic)
lowers the coefficient of sliding friction
by 90%. TEGO Glide 482 has been
specially developed to optimize the slid-
ing resistance of waterborne coatings.
The slip additive emulsion is much more
They must also exhibit sufficient compati- The best slip additives are therefore, effective here than homogeneously
bility in the binder, otherwise cloudiness polyethersiloxanes with high levels of soluble slip additives.
or flow defects can occur in the liquid polydimethylsiloxane segments, such as
coating and/or dried film. TEGO Glide 410. If, however, a slip effect combined with
intercoat adhesion is required; TEGO
Glide 450 is recommended. This poly-
Measurement of slip properties Measurement of release effect ether siloxane has been successfully used
in delicate clear coats. TEGO Glide 432
A test in which frictional force is mea- The release characteristics of siloxane shows its strengths in radiation-curing
sured has proved suitable for measuring containing additives are measured by coatings and printing inks. Its combination
slip properties. The Measurement of slip applying standardized adhesive strips to of substrate wetting, improvement of
properties video on our homepage the coating surface. The prepared test scratch resistance and low-foam is
shows the procedure. A 500 g weight is specimen is aged, partly with a weight impressive. TEGO Rad products, which
drawn uniformly on a felt substrate over applied. The adhesive strips are then are reacted into the coating, achieve a
the coating surface by a tensile testing linked to a sensor and pulled off the sur- significantly greater slip effect in radia-
machine. The force required is measured face at constant speed. The force required tion-curing systems. TEGO Rad 2300 is
by a transducer. The friction between two to remove the adhesive strips is measured particularly suitable for use in clear coats
coated/printed surfaces can be deter- and used to calculate the release value. and combines substrate wetting, slip,
mined by varying the geometry slightly. The lower the pull-off force, then the compatibility and low-foam characteris-
This test is conducted at constant speed stronger the release effect. Non-reactive tics, etc. In contrast, TEGO Rad 2600
and permits highly accurate and repro release additives may migrate into the combines deaerating characteristics and a
ducible measurements. The sliding resis- adhesive either over a period of time or strong release effect.
tance is particularly low if the interactions because of the effect of temperature
within the lubricant film and between so that the release effect disappears.
the film and sliding body are small.

page 74 Technical Background_Slip and Flow Additives_Radiation-curing Additives


What affects friction?

If an object is pulled over and parallel to a


substrate, a certain force must be over-
come at the start. This initial force is
termed static friction. This adhesive force
prevents two touching objects moving in
relation to each other.

To maintain movement, the sliding fric-


tional force must be overcome. The slid-
ing frictional force required (FR) is pro-
Figure 10: Measurement of release effect (schematic)
portional to the normal force (FN) of the
object. The various material properties
involved affect the dimensionless coeffi-
cient of friction (G).

FR = G FN What is the effect of being able to


chemically incorporate TEGO Rad
What is the effect of polyether
modification?
products? Polyether modification of flow and slip
There is thus a coefficient of static friction The release effect becomes more durable additives primarily increases the compati-
(H) and a coefficient of sliding friction by crosslinking into the binder matrix. bility of the additives with coating sys-
(G); the former is the greater. The mate- The surface effects of additives which tems. The siloxane component of the
rial properties of the substrate and of the cannot be chemically bound decrease on additive is responsible for the extreme
object to be moved are reflected in the aging. surface activity. The modification mini-
coefficients of friction. The chemical mizes the tendency of cloudiness and pre-
composition and the interactions arising Why are crosslinkable slip additives dif- vents undesirable side effects which are
from it as well as the surface morphology ficult to overcoat/overprint? known to occur with pure silicone oils.
(roughness) play a role. Upon curing, reactive additives are chemi-
cally incorporated in the binder matrix What are the advantages of acrylates
which impairs intercoat adhesion during over polyethersiloxanes as flow
overpainting/overprinting. Unimpaired additives?
adhesion requires mobility of the addi- The acrylates barely influence the surface
FAQs tives. A fresh coating applied to a film, tension. Primers containing polyacrylates
treated with additive, must be able to dis- can be rewetted because the polyacry-
How can additives improve scratch solve the additive from the lower layer to lates do not reduce the surface energy
resistance? allow problem-free adhesion. If the addi- even in cured coatings formulations.
Improving the coating's slip and smooth- tive is chemically anchored, this is not
ness enables objects to slide past the possible.
surface. Scratches are avoided since the
offending object slides away instead of
penetrating the surface. The crosslinking
density is not affected.

Technical Background_Slip and Flow Additives_Radiation-curing Additives page 75


Substrate Wetting Additives
TEGO Wet TEGO Twin
How well a paint wets the substrate is a The interfacial tension of a liquid/air
determining factor in the quality of a interface is termed surface tension.
coating. How can wetting during applica-
tion be improved? Which is the best addi- To bring a molecule from inside a liquid
tive for a particular problem? What is the to the air interface requires energy. The
mechanism behind it? We are often asked surface of the liquid is enlarged. Attrac-
these and similar questions which reflect tive forces act between the molecules of
the importance manufacturers of coatings the liquid. Inside the liquid, these forces
and printing inks attach to the subject of cancel each other out as they act uni-
wetting. Hardly a surprise, as a homoge- formly in all directions. At the interface,
nous, continuous film cannot form if the situation is different. The resulting
wetting is inadequate during application force is oriented towards the interior of
or drying. the liquid; the liquid tries to reduce its
surface area. Ideally, the liquid adopts a
There is no categorical answer to the spherical shape because this gives the
questions raised above; possible defects lowest surface or interfacial area for a
must be considered individually. A more particular volume. In general, the force
detailed approach requires the properties acting on the surface of a liquid phase
of the substrate and the coatings to be (interfacial tension) causes liquids to
considered. strive for the minimum surface area.

Figure 1: Water skater supported by surface Figure 2: Wetting on a low energy substrate as displayed on the left with substrate wetting additive
tension

Technical Background_Substrate Wetting Additives page 77


A B C

F1 > F2
F1 F2
Figure 3: Interactive forces at the water/air interface or water/air/surfactant interface.
(A) - Inside the liquid, the attraction forces between the molecules cancel each other out. (B) - At the surface the resulting force (surface
tension) is directed towards the interior of the liquid. (C) - A surfactant reduces this force (surface tension).

The work required to increase an interfa- The SI unit for the surface tension is N/m 73 mN/m. The surface tension of ready-
cial area A by unit amount is termed inter- and is the result of the conversion of to-use coatings naturally depends not
facial energy W. It is proportional to the Joules as follows: only on the solvent used but also on the
size of the additional unit and can be for- other constituents. Nonetheless, the sur-
mulated as a differential: J Nm N face tension is an important parameter.
1 m2 = 1 m2 = 1m
=dA
dW
The surface tension of liquids can be
determined directly. The surface tensions
The measuring tech-
The quotient is defined as surface ten- of solvents typically used in coatings nique
sion. It has the dimensions of energy per range from 20 to 70 mN/m. Highly vola-
unit area (J/m2) and is therefore the work tile, lower aliphatic test spirits exhibit the In the best known technique for measur-
required to obtain a new surface. lowest values, that of pure water is ing surface tensions of liquids, the du
Noy Ring Method, a platinum-iridium
ring is placed into the liquid so that the
surface is completely wet. Upon slowly
Surface tension of various liquids
withdrawing it, a lamella is formed which
Liquid Surface tension (mN/m) constitutes an increase in the surface of
the liquid. The maximum force required
Water 73
to pull this lamella is a direct measure of
Alkyd resins 33 60 the static surface tension as it corresponds
Butyl glycol 30 to the energy necessary to increase the
Toluene 29 surface of the liquid (lamella). This mea-
suring technique is shown on our homep-
Isopropanol 22
age (video Measurement of static surface
n-Octane 21 tension).
Octamethyltrisiloxane 17

Hexamethylsiloxane 16

Isopentane 14

page 78 Technical Background_Substrate Wetting Additives


Figure 4: Measurement of
dynamic surface tension
with the bubble pressure
tensiometer
Figure 5: Measurement of static surface tension by the du Noy method

This method is suitable for investigating introduced into the liquid under investiga- the new interfaces which are formed very
aqueous solutions containing surfactants tion via a capillary. In this process, the rapidly. That is why measuring surface
or of waterborne or solventborne pressure required to generate the new tension under these dynamic conditions is
clearcoats. Pigmented systems do not give interface of the liquid passes through a also useful.
reliable data as the presence of pigments maximum which is directly related to the
impairs lamella stability so that the values dynamic surface tension. This method Unfortunately, the results from pure
of surface tension appear to be too low. evaluates the mobility of the surfactant in aqueous solutions of surfactants cannot
Insoluble additives, such as defoamers, the medium since the surfactants must be transferred directly to coatings sys-
can also cause misleading results. orient as quickly as possible at the newly tems. It is therefore advisable to check the
formed interface to maintain the surface effect of wetting agents in the coating or,
The dynamic surface tension can be tension at a constant low level. When at least, relevant binders.
determined using a bubble pressure applying coatings, during printing pro-
tensiometer in which gas bubbles are cesses for example, substrate wetting
generated at a defined pressure and agents must be able to orient quickly to

Laws governing wetting of the sur-


faces of solids
In contrast to the surface energy of the
S LS liquid phase of the paint, that of the sub-
L strate cannot be measured directly. A
L
number of indirect methods have been
S LS developed; one of the most important
being measurement of the contact angle
of various test liquids on the substrate.

Figure 6: Relationship between the surface tension of a liquid droplet on a


substrate and the measured contact angle

Technical Background_Substrate Wetting Additives page 79


Surface energy of substrate surfaces How to improve wetting

Substrate Surface energy (mN/m) Wetting can be influenced by the sub-


Steel ~ 50 strate surface and via the formulation of
Aluminum ~ 40 the coating. In principle, a solid surface
always wets out well if the surface ten-
Polyester 43 45
sion of the liquid is low compared to the
Polyethylene/LD 36 free surface energy of the substrate.
Polyethylene/HD 32 Substrates with low surface energies
Polypropylene 30 34 include polyethylene, polypropylene and
Teflon; examples of high energy surfaces
Paraffin wax 26
are metals, metallic oxides and glass.
PTFE (Teflon) 20 Cleaning of metallic substrates removes
grease and increases their surface energy.
Corona treatment of the surface of plas-
tics has a similar effect: a more energetic
surface zone is generated by oxidation.
Not only the material, but also its surface
Wetting of solids by liquids is influenced basis for a qualitative description of all texture plays a role and this can be uti-
by the surface tension of the components wetting phenomena. In general, the fol- lized in some cases.
involved. Thomas Young established a lowing rules, confirmed in practice,
formula in 1805 which characterizes the apply: The most widely used method for
surface tension at the three phase contact a substrate with high surface energy is improving wetting is the addition of
of a droplet on a solid. easily wet out substrate wetting additives to the liquid
a liquid with a low surface energy is phase. These surface active compounds
Youngs equation assumes all forces are in good at wetting attach themselves preferentially to the
equilibrium and, strictly speaking, only wetting is ideal if the surface energy of phase boundary where they reach a
applies to the case of thermodynamic the liquid is significantly less than the higher concentration than in the bulk
equilibrium. Nevertheless, it forms the surface energy of the substrate phase.

Evonik offers substrate wetting additives


which, when used in even minimal
amounts, substantially lower the surface
tension of the liquid coating so that even
difficult substrates can be wet out.
spreading no wetting

Contact angle

The contact angle between a liquid and a


solid is widely used as a criteria to evalu-
ate the wettability. The term wetting is
1 2 3 4 5
considered to mean the formation of a liq-
uid/solid interface in place of the original
Figure 7: Relationship between contact angle and wetting characteristics
solid surface/gas interface.

page 80 Technical Background_Substrate Wetting Additives


Composition and mode of action of The differences in molecular structure are
reflected in product recommendations:
substrate wetting additives TEGO Wet 240particularly suitable for
waterborne formula-
tions, fine atomization
during spray application
TEGO Wet 270outstanding anti-crater-
The task of all substrate wetting additives How do silicone surfactants behave in ing effect, additional
is to reduce the surface tension of the liq- waterborne, solventborne and uv-cu- flow promotion
uid phase. As surfactants, their interfacial ring coatings?
concentration is increased by at least a In completely waterborne systems, the
factor of 100 compared to that of the vol- Short chain polyether siloxanes are used effectiveness of short-chain siloxanes is
ume phase. The reason for this strong primarily to reduce surface tension in completely sufficient; whereas in solvent-
adsorption is their chemical structure. As waterborne coatings. The reason is the borne and uv coatings, a longer siloxane
amphiphilic substances, surfactant mole- high surface tension of water which is the chain is advantageous.
cules combine at least a hydrophilic and a main solvent in such systems.
hydrophobic part.
The structure of a siloxane surfactant is Siloxane-Gemini surfactants
This structure is also responsible for their shown schematically in fig. 9. The poly-
preferential orientation at the interfaces: ether modification substantially influences Gemini surfactants are distinguished
the hydrophobic part is forced out of the the compatibility and tendency to foam of chemically by a combination of two
volume phase. The hydrophilic part points surfactants. The length of the silicone hydrophobic side chains and two ionic or
towards the water phase. This arrange- chain determines the interfacial activity of polar chains separated by a spacer. Gemini
ment of the surfactant molecules forms a the substrate wetting additive. The higher surfactants are interesting because of
new low energy coating surface which the siloxane content in the molecule, the their particularly high surface activity and
can easily wet the low energy surface of stronger the reduction in surface tension. their different aggregation characteristics
the substrate. compared to classic surfactants.

air
O O O
Si Si Si Si

n m surfactant

O (EO )0 CH3
Figure 9: Schematic structure of a polyether siloxane

water

Figure 8: Orientation of surfactants at the interface

Technical Background_Substrate Wetting Additives page 81


Reduction in surface tension of a waterborne binder Spreading of 0.05 ml of a 0.1% aqueous solution on
by surfactants a PVC sheet

Surfactant Surfactant surface tension (mN/m) Surfactant Wetted area (cm2)

High molecular silicone High molecular silicone surfactant 5


surfactant 31
Organic wetting agent 20
TEGO Wet KL 245 21
TEGO Wet KL 245 160

Using this clever combination, researchers


at Evonik have succeeded in linking Gem-
Typical applications of For all these classes of substances, there
are specific areas of application.
ini surfactant chemistry with silicone individual products
chemistry. The advantages are the charac- Short chain, polyether-modified siloxanes
teristics of Gemini technology combined The optimum surface active substrate are similarly effective in reducing static
with the performance and low surface wetting additive for a particular applica- surface tension. They are almost universal
tension of siloxanes. tion is decided, in the final analysis, by the aids for difficult to wet and contaminated
requirements of the users of coatings and substrates in diverse areas of application
With siloxane-based multi-functional sur- printing inks. Basic research, user experi- (see also Contamination test video). On
factants, Evonik has opened a new door ence and practical testing have played capillary substrates, such as wood, they
to substrate wetting without foam. their part in developing additives which, greatly improve pore wetting by the coat-
because of their special characteristics, ing. Their particular advantage is the abil-
The effect of these products is particularly provide the right solution to many chal- ity to customize properties such as com-
advantageous in waterborne formulations. lenges. patibility, low foam and anti-cratering
TEGO Twin products have also proved to effects via polyether modification and
have interesting and beneficial effects in The products currently offered by Evonik siloxane chain length.
solventborne systems. comprise the following classes of chemi-
cal substances: Low molecular weight polyether-modi-
TEGO Twin 4000 and TEGO Twin polyether-modified siloxanes fied siloxanes, such as TEGO Wet 270
4100 are two powerful products with siloxane multi-functional surfactants and TEGO Wet 240 reduce the surface
very different application properties. alkoxylates (silicone-free) tension in waterborne systems more
strongly than hydrocarbon-based surfac-
tants or higher molecular weight poly-
ether siloxanes. This makes them ideal
substrate wetting additives for coating
many critical substrates. TEGO Wet 270,
with its relatively high silicone content,
has excellent anti-cratering properties and
is outstanding at improving wetting of
wood substrates. TEGO Wet 240, spe-
cially developed for spray paints, provides
optimum atomization during application
without affecting the slip characteristics
of the dried finish.

Figure 10: Waterborne


clearcoat on a critical
substrate, optimized
with Tego Twin 4100

page 82 Technical Background_Substrate Wetting Additives


Substrate wetting additives occasionally At the end of the day, however, the spe- Which additive achieves the best result
lead to the incorporation of foam since cific use of the coating defines which with spray application?
the more effective a surfactant is at reduc- additive is best for solving problems. Tego Wet 240 has been specifically
ing surface tension, the greater the ten- developed for particularly fine mist and
dency to foam. With Evoniks proprietary outstanding atomization. The small drop-
know-how, our researchers have been
able to extend the existing range of Tego
Outlook lets substantially improve substrate wet-
ting.
products with the addition of the multi-
functional surfactants TEGO Twin 4000 The importance of substrate wetting Which substrate additive is the preferred
and 4100. This new type of product pro- additives is growing and goes hand in choice for reducing dynamic surface ten-
vides a combination of outstanding reduc- hand with the development of eco- sion?
tion in surface tension and pronounced friendly coatings formulations based on TEGO Wet 500 is the additive of choice
defoaming properties. Tego Twin 4100 new raw materials and application con- for reducing dynamic surface tension in
is a highly compatible, foam inhibiting cepts. Additives with optimized perfor- dynamic processes such as printing. Fur-
multi-functional surfactant imparting mance tailored to solve specific problems thermore, the product does not stabilize
good recoat properties. are being developed to make application foam.
more secure and broaden the application
The TEGO Wet 500 series, a silicone- window. How can defoaming be combined with
and solvent-free class of surfactants offers wetting?
advantages particularly in printing inks TEGO Twin 4100 based on the unique
since they reduce dynamic surface tension
significantly. The TEGO Wet 500 range
FAQ: siloxane multi-functional technology
combines wetting properties with foam
of products is also foam inhibiting and inhibition as required in low-VOC coat-
degassing in waterborne coatings and Which additives remove craters in ings. Despite high activity, recoatability is
printing inks. TEGO Wet 505 is the most waterborne coatings? good.
hydrophobic surfactant in this class of TEGO Twin 4100 and TEGO Wet 270
products. It acts as a deaerator and wets are particularly suited to reduce surface
pigments. Within this group, the hydro- tension and eliminate craters. They are
philic TEGO Wet 510 is the most effec- also highly capable in completely wetting
tive as far as substrate wetting and pro- inhomogeneous substrates such as wood.
moting flow are concerned.

Characteristics of substrate wetting additives

Reduction in static surface Reduction in dynamic surface


Substrate wetting additive tension tension Low foam

TEGO Wet 500 series, si-free satisfactory very good very good

TEGO Wet 240, contains si very good satisfactory satisfactory

TEGO Twin 4100 very good satisfactory very good

Technical Background_Substrate Wetting Additives page 83


Wetting and Dispersing Additives
TEGO Dispers

Seite 84 Technischer Hintergrund_Netz- und Dispergieradditive


Optimal dispersion and stabilization of sible. Only then can color intensity, gloss,
pigment particles is a significant factor in hiding power, lightfastness and weather-
determining the end properties of lac- ing resistance be maximized. Pigment dis-
quers, paints or printing inks. The pig- persion and stabilization, which requires
ments and fillers of the formulation must time and energy, is hardly possible with-
be ground to small-sized particles, wetted out suitable wetting and dispersing addi-
and uniformly distributed as stably as pos- tives.

What occurs during dispersion?

Pigment dispersion can be broken down where


into three steps which occur partly con-
secutively and partly concurrently: wet-
s : free surface energy of the solid
ting, dispersion and stabilization. sl : Interfacial energy solid/liquid
l : Surface tension of the liquid
Wetting : Contact angle solid/liquid

Wetting the pigment particles is essential With spontaneous wetting or spreading,


for them to be finely distributed in a liq- the contact angle is zero so that the cosine
uid. Air entrapped in the pigment powder term is 1. This occurs when:
must be fully removed and the pigment
particle completely surrounded by the liq- s sl = l
uid medium. The processes involved in
wetting a solid are approximately
described by the Young equation:
For the liquid to wet the solid, the surface
tension of the liquid must be lower than
s = sl + l cos that of the solid. A liquid with lower sur-
face tension wets pigments better than
or one with higher surface tension. An addi-
s sl = cos tive which promotes wetting must there-
fore primarily reduce the surface tension
l of the liquid.

Technical Background_Wetting and Dispersing Additives page 85


However, wetting and dispersing addi- lowers the viscosity of the millbase. This Every dispersion process to break up
tives do not only lower the surface ten- allows higher pigment loadings to be aggregates and agglomerates requires
sion of the liquid. As their pigment affinic achieved, which is particularly important energy. The work needed is given by:
groups cause them to be adsorbed onto for the mechanical dispersion process.
the pigment surface, they also alter the Millbase formulations which have been dW = dA
boundary surface. The surface tension is optimized in this manner are suitable for
no longer that between pigment and liq- all modern grinding equipment such as where
uid but between additive and liquid. dissolvers, bead mills and three-roll mills. W: interfacial surface energy
: surface tension
Wetting and dispersing additives lower In the dispersion process itself, the pig- A: interface area
the surface tension of the liquid and the ment agglomerates are broken up into
interfacial tension between pigment and primary particles and smaller pigment This equation indicates that, for an
liquid so that wetting is promoted in two aggregates. Usually aggregates cannot increase of the surface dA during disper-
ways. be broken up. The primary particles in sion (by breaking up agglomerates), an
aggregates are so strongly bound surface energy input dW is needed which is pro-
to surface that it is practically impossible portional to the surface tension . The
Dispersion to break them apart. Account is taken of smaller the surface tension, the greater
this in pigment manufacture and the the increase in surface area for a particular
The pigment particles are now wetted by proportion of aggregates specifically amount of energy applied. Equally, for a
the surrounding binder solution and their controlled. Their amount can affect the particular change in surface area in the
surface coated with the surface-active color tone of a pigment. presence of a dispersing additive (that is
additive. The additive reduces the interac- at reduced surface tension) less dispersion
tions between the pigment particles and energy is needed.

page 86 Technical Background_Wetting and Dispersing Additives


Stabilization Dissociation of the adsorbed additive with pigment-affinitive groups are used.
molecules into bound anions and freely These groups attach themselves to the
In the dispersion process, the aggregates moving cations forms an electrochemical pigment surface and thus ensure adsorp-
(fig. 1a) are broken up into primary parti- double layer around the pigment parti- tion of the additive. The polymer seg-
cles and smaller agglomerates. Formation cles. Each pigment particle is situated in a ments are responsible for compatibility in
of primary particles results in an increase solution of oppositely charged ions which organic systems. They also stabilize the
of the boundary area with the liquid are relatively firmly bound to the pigment. dispersion by protruding into the solvent.
medium (fig. 1b). The higher the interfa- Both attractive and repulsive forces If the pigment particles come too close,
cial tension, the more strongly will a solid depend on the interparticle separation. the polymer segments interpenetrate and
attempt to reduce the interfacial area. The With a strongly pronounced double layer, their mobility is reduced, thus lowering
particles, therefore, reagglomerate to repulsion predominates and the disper- the entropy. The pigment particles sur-
form so-called flocculates (fig. 1c). The sion is stable. If the electrochemical dou- rounded by the polymers move away
term flocculate indicates an agglomerate ble layer is disrupted, for example by from each other to balance this entropy
occurring in suspension. Dispersing addi- addition of an electrolyte, attractive forces loss.
tives suppress the formation of floccu- dominate and the dispersion breaks up.
lates. Electrostatic interactions can be quantita- With the complex demands made of wet-
tively described by the zeta potential, , ting and dispersing additives, it is useful
To stabilize the fine distribution of parti- which is a measure of the potential at the to combine electrostatic and steric effects.
cles, the additive molecules must be shear layer of a moving particle in a dis- This is often known as electrosteric stabi-
firmly adsorbed onto the pigment surface. persion. As approaches zero, the ten- lization.
This means that the additive molecules dency of the particles to agglomerate
require groups or segments which can increases Modern wetting and dispersing additives
interact strongly with the pigment surface for waterborne application use elec-
by ionic bonding, dipole interactions or Solventborne paint systems cannot be trosteric stabilization. Only such additives
hydrogen bridges. Depending on whether stabilized electrostatically. Particle floccu- can fulfill the high demands made on sta-
the formulation is water- or solventborne, lation is instead preferably prevented by bilization and durability.
various mechanisms are possible. steric stabilization. Polymeric additives

In waterborne coatings, electrostatic


repulsion is traditionally the most impor-
tant stabilizing factor. Interactions within
the formulation can be described by the a b c
DLVO-theory (named after Derjagin,
Landau, Verwey and Overbeek). In inter-
preting the stability of waterborne disper- air
sions, the interplay between attractive
and repulsive forces is considered.

liquid liquid liquid

Figure 1: Schematic representation, (a) agglomerated, (b) dispersed, (c) flocculated pigments

Technical Background_Wetting and Dispersing Additives page 87


electrostatic stabilization steric stabilization electrosteric stabilization

dispersed dispersed dispersed


particle particle particle

Figure 2: Stabilization
of dispersed particles:
(a) electrostatic
(b) steric
(c) electrosteric

A further possibility of preventing pig- change in the rheological properties: at


ment particles approaching each other rest, the viscosity is very high so that the
and thereby flocculating is controlled pigments can no longer easily precipitate.
flocculation. In this, the structure of the The different mobility of the pigments,
additives allows them to mutually interact. which is also partly responsible for flood-
The individual additive molecules adsorb ing and floating, is prevented by pigments
onto the pigment surface and by interac- binding to flocculates of the same color
tion with each other form a three-dimen- (fig. 3).
sional network. This network causes a
However, the three-dimensional network
can compromise the flow of the coating
and thus reduce gloss. Controlled floccu-
Figure 3: Simplified diagram (not to scale) of controlled flocculation lation is therefore mainly used in solvent-
by crosslinking of the additive molecules borne primers and fillers. This method is
Network formed by secondary valences not used for waterborne coatings; a simi-
lar effect can be achieved there with asso-
ciative thickeners.

organic pigment inorganic pigment

page 88 Technical Background_Wetting and Dispersing Additives


Structure of wetting and dispersing desired multifunctionality necessitates
deliberate combinations of different wet-
additives ting agent components.

In principle, every wetting agent has one


Wetting and dispersing additives are wetting agents are of low molecular or more adhesion groups which can
amphiphilic compounds, i.e. they are both weight and dispersing additives are of dock with the pigment and a more-or-less
hydrophilic and lipophilic. Their special high molecular weight. Because of the long segment which can be solvated. This
molecular structure allows them to enable complexity of amphiphilic substances, general principle is shown in the follow-
or facilitate dispersion of pigments and which contain unique functional groups, ing simplified schematic diagram:
fillers in the solvent. In addition, they it is not easy to develop a simple model.
should stabilize the dispersion. The boundaries are not fixed as the

Wetting and dispersing additives can be


classified in different ways. In the litera-
interfacial active compounds
ture, there are assignments according to
chemical structure or separation into ionic
anionic [R - (CnH2n) - COO] -K+
and non-ionic products. Other classifica-
tions are made by field of application,
cationic [R - N - (CH3)3]+Cl-
waterborne or non waterborne, or by pig-
ment type, organic or inorganic. A classi-
amphoteric R3 - N+- CH2 - COO-
fication by molecular size is also possible:

non-ionic R - O - (CH2 - CH2- O)n - H

Figure 4: Schematic diagram of the structure of surfactant compounds with various types of head groups

Technical Background_Wetting and Dispersing Additives page 89


The number of adhesion groups is among long-term stabilization of dispersions. Oligomeric and polymeric dispersing
those properties important for the effec- Inorganic pigments can also be split into additives are particularly suited for steric
tiveness of a wetting and dispersing addi- chemical classes. With a few exceptions stabilization. It has been found that block-
tive. Adhesion groups are functional these are oxides, oxyhydroxides, sul- and graft-copolymers are better than
groups which have a special affinity for phides, silicates, sulphates or carbonates3. homo- or copolymers with a random
pigment surfaces. If there is only one These pigments are characterized by polar statistical distribution. Pigment affinic
adhesion group per molecule of dispers- molecular structures so that their interac- groups are incorporated in the additive
ing additive, replacement by a solvent tion with acid groups, such as carboxy, depending on the type of pigment and the
molecule leads immediately to complete phosphate or sulphate, are particularly application (fig. 5).
removal of the additive molecule from the strong.
surface. This leads to flocculation of the Modern high performance polymeric
pigment. Additives with several functional Carbon blacks are a special case. The sur- wetting and dispersing additives suitable
groups cannot so easily be removed and face area of these pigments is many times for all types of pigments have multiple
therefore show especially high perfor- greater than that of organic or inorganic occurrences of all types of adhesion
mance. pigments. On the one hand, a much larger groups, e.g. TEGO Dispers 755 W.
amount of dispersing additive is needed
The type of adhesion group depends on to cover the surface effectively. On the
AB block copolymer
the particular pigment surface: other hand, carbon black has neither a
Organic pigments usually contain aro- classic organic/aromatic nor an inor-
matic groups so that dispersing additives, ganic/crystalline structure. Experience pigment affinic very soluble

which contain, for example, phenyl or has shown that nitrogen-containing dis-
napthyl units, are particularly suitable for persing additives are the most successful.

BAB block copolymer

very soluble pigment affinic very soluble

AB block copolymer

AB block copolymer graft copolymer


pigment affinic very soluble
very
soluble
pigment affinic very soluble

BAB block copolymer


pigment affinic

BAB block copolymer


very soluble pigment affinic very soluble
Figure 5: Copolymers for
steric stabilization
very soluble pigment affinic very soluble

graft copolymer

very
graft copolymer soluble

very
soluble

pigment affinic

pigment affinic

page 90 Technical Background_Wetting and Dispersing Additives


The function of wetting and dispersing on the scattering power of the pigment
and the refractive index of the pigment
additives with the surrounding medium (usually
the film forming agent). In a coating with
strong hiding power, the pigment parti-
Wetting and dispersing additives lower the pigment. The smaller the pigment cles scatter the light so strongly that it
the viscosity of a coating formulation. particles, the greater their effective sur- hardly reaches the substrate. If residual
However, that is not their only effect. face area and consequently the higher light is reflected from the substrate, it is
This class of additives has a marked effect their absorbing power. A higher absorb- so strongly scattered that it does not reach
on a whole series of different, essential ing power is associated with higher color the eye. For a coating to scatter the light
characteristics of the formulation. intensity. To ensure that the small pig- optimally, an even, fine distribution of the
ment particles remain finely distributed pigment stabilized by dispersing additives
and do not clump together to form larger is essential.
Color intensity flocculates, they must be stabilized. Dis-
persing additives are necessary for this.
The color intensity is a measure of the Flocculation
ability of a pigment to absorb incident
light and impart color to a medium. It has Hiding power Flocculation is the reagglomeration of
practical importance in coloring white already dispersed particles. In the disper-
base paints: the stronger the color of a The hiding power of a coating is its ability sion process, energy is taken in to break
tinting agent, the more economical it is. to cover the color or the color difference up the pigments and form new surfaces.
The color intensity of such a preparation with the substrate.1 How well the sub- This is, however, an unstable state and floc-
depends significantly on the absorbing strate is hidden depends on the coating culation can occur at any time during man-
power and the average particle size of thickness, the color of the substrate and ufacturing, storing and applying a paint.

Technical Background_Wetting and Dispersing Additives page 91


Pigments also tend to flocculate after the affect leveling. Poor leveling decreases This vertical flooding, also known as
paint has been applied to a surface car- the gloss further. Since wetting and dis- floating, causes the film to appear more
bon black with its high surface area is persing additives inhibit flocculation, they colored than desired. Flooding can be
particularly susceptible. If this occurs, increase the gloss of a coating. made visible by rub-up tests.
a substrate cannot be evenly coated in
black. Dispersing additives inhibit floccu- Horizontal flooding occurs by separation
lation of the pigment particles. Flooding and floating of the color pigments in the drying film
and originates from solvent flows: parti-
These phenomena occur with mixed pig- cles with lower density are entrained with
Gloss ments when the density and/or the parti- the solvent flow and islands with different
cle sizes of the pigments are markedly dif- pigmentation result. These so-called
Light falling on a surface can be reflected ferent. Bnard cells are clearly visible.
directly (specular reflection) or diffusely.
High gloss is obtained when the surface With its high density, titanium dioxide This unwelcome separation of pigment
is very smooth and the diffuse component tends to concentrate at the bottom of the particles can be prevented if they are
of the reflection is small. Pigment parti- drying paint film. Organic colored pig- associated with each other in a controlled
cles or flocculates which protrude from ments have significantly lower density manner by suitable dispersing additives
the surface interfere with the specular than titanium dioxide and, therefore, con- which induce controlled flocculation.
reflection. Flocculated pigments also centrate in the upper part of the film.

page 92 Technical Background_Wetting and Dispersing Additives


Evaluation of particle size in the grind guage

Evaluation of wetting and dispersing additives

Particle size With a little practice, the grind guage


allows quick and simple measurement of
The primary criterion which decides the the maximum particle size. However, the
quality of a dispersion is the particle size particle size distribution cannot be mea-
distribution. By measuring the particle sured in this way. The grindometer is of
size or the size of the largest particle, the no use for binder-free dispersions which
endpoint of a dispersion process can be dry very quickly or for particle sizes less
very well established. The grindometer is than 5 m.
the simplest method of measuring the
maximum particle size of inorganic pig- Very small particles and particle size dis-
ments. A sample of the millbase is tributions can be studied with more
brushed onto a grindometer. Large parti- sophisticated measuring methods such as
cles are moved by the doctor blade and laser diffraction or ultrasound. However,
produce stripes in the draw down. The because of their high cost, these methods
size of the largest particles can be read are generally unsuitable for routine use in
directly from a scale. the laboratory.

Technical Background_Wetting and Dispersing Additives page 93


Whether or not the desired particle size very time-consuming but delivers mean- Color intensity according to Kubelka-
has been reached can be easily deter- ingful comparative data and is used mainly Munck:
mined using secondary indices. Thus, by pigment manufacturers.
with organic pigments, the color intensity
K (1R)2
is dependent on the particle size. By mea- An absolute value can be obtained by a FS = =
suring the color intensity at various times method based on a theory by Kubelka- S 2R
during dispersion, changes in color inten- Munck, involving the ratio of reflectance
sity can be followed and the end point of and transmission. The sum of the reflec- with
the dispersion determined. tance values over the complete wave FS: Color intensity
range gives a value for the color intensity. K: Absorption coefficient
S: Scattering coefficient
Color intensity In practice, however, this method has a R: Reflection at infinite film thickness
systematic error as it is based on the (no change in the degree of reflec-
To determine the color intensity, a sample assumption of an infinite film thickness tion)
of the millbase is let down in a suitable and a constant degree of reflection. It is
paint formulation. Assessment is made by not suitable for qualitative assessment of
comparison with the same amount of a a pigment batch. Rub-Up
standard millbase optically or using a
spectrophotometer. The amount of mill- The Rub-Up test is used to test the stabili-
base is adjusted until both samples have zation of pigment particles. It allows the
the same optical properties. The relative compatibility of pigment concentrates,
color intensity of the sample as a percent- tendency to flocculation of pigment parti-
age of the standard is calculated from the cles and flooding phenomena to be deter-
various amounts used. This method is mined. A part of the wet, but already

page 94 Technical Background_Wetting and Dispersing Additives


rying, film is rubbed with a finger or
d important indicator of the stability of a If problems still occur
brush. If the pigment particles have pigment concentrate. If it alters during
demixed or are strongly flocculated, the storage, the pigments are usually inade- In spite of innovative and high perfor-
mechanical rubbing re-establishes a quately stabilized. mance wetting and dispersing additives,
homogeneous distribution. In a drying pigment dispersion is not easy. Unex-
film, the viscosity has already increased The dynamic viscosity of a millbase can pected problems often occur especially
strongly and the re-established homoge- be quickly and simply determined using a with waterborne formulations. We will be
neous distribution of the pigment parti- Brookfield viscometer. This method can, happy to give help and advice to enable
cles is thereby stabilized. The extent of however, only be used for quality control. you to utilize the full effectiveness of our
pigment separation or flocculation is Millbases show pseudoplastic flow behav- additives.
obtained from the color difference ior. Changes in their viscosity are depen-
between the rubbed and non-rubbed dent on the applied shear energy. To
film. The color difference is usually obtain an exact picture of the rheological
quoted as the separation of the color behavior of a millbase, a complete flow
chromaticity, E, which is dimensionless. curve must be obtained using a rotational
If E is less than 0.5, no color difference viscometer which can measure the viscos-
is visible, between 0.5 und 1.0 the color ity of the millbase at different shear rates.
difference is only slightly visible, but a E
larger than 1 is not acceptable. Such a flow curve provides information
about the rheological behavior of the
material from manufacture through trans-
Viscosity port to application. Interactions in the dis-
persion can also be quickly detected.
Literature:
The viscosity of a millbase must be suit- 1
DIN 55987: 1981-02
able for the dispersion unit. If the millbase Detailed information about the theoretical 2
W. Herbst, K. Hunger, Industrial Organic
Pigments, VCH Verlagsgesellschaft mbH,
viscosity is too high, the unit can be dam- basis of viscosity and rheological behavior Weinhein, Germany, 1993, p. 4ff
aged. If it is too low, insufficient shear can be found in Technical Background: G. Buxbaum, Industrial Inorganic Pigments,
3

VCH Verlagsgesellschaft mbH, Weinhein,


force will be transferred to break up the Rheological Additives. Germany, 1993, p. 9
pigment agglomerates. Viscosity is also an

Technical Background_Wetting and Dispersing Additives page 95


Rheological Additives
TEGO ViscoPlus

Seite 96 Technischer Hintergrund_Rheologieadditive


Panta Rhei Greek for everything flows
certainly applies to paints and coatings.
Rheology
From manufacture through storage and
processing to drying or curing after appli- Rheology (Greek: rheos = flow or Energy must be supplied continuously to
cation, many different demands are made streaming, logos = word/science) is the maintain the flow of a liquid. Viscosity ,
on a coating or printing ink, related to its study of deformation and flow of sub- the most frequently used rheological
flow properties. Characteristics which are stances. Flow is the continuous deforma- parameter, is calculated from the shear
affected include: tion of a material under the influence of rate and the shear stress t. Basic rheo-
settling/sedimentation (important for external forces. Various rheological mea- logical parameters are explained in terms
storage stability) suring methods can be used to characte of the two-plate model (fig. 1).
brushing resistance rize coatings.
spattering The upper plate of area A is movable and
sprayability The quantities measured in rheological the lower plate stationary. The plates are
sagging investigations are forces, deflections and separated by a distance h which is filled
flow velocities. Viscosity is the resistance of a with liquid. When a certain force F is
liquid to forced, irreversible change of applied the upper plate reaches a velocity
In solventborne formulations, the flow position of its volume elements. v which is related to the shear stress.
properties can be completely regulated
via the molecular weight of the dissolved
binder. In waterborne formulations, the
binder is in the form of dispersed polymer
particles so that regulation of the flow
behavior by changing the molecular
v
weight is not possible. Rheological addi-
tives (thickeners) must therefore be used F
to adjust the flow properties of water-
borne coatings and printing inks. v (h)  (h)

Figure 1: Flow in the gap between two horizontal parallel plates moving relative to each
other.

Technical Background_Rheological Additives page 97


The two characteristic values, shear Shear rate for selected, technical coatings demands
stress, t, and shear rate, , can be derived
from the two-plate model. The shear
stress has the dimensions of pressure and
is defined as the shear force F [N] per
shear area A [m] where the force is par- settling
allel to the surface. The unit is the Pascal
leveling
(Pa) which is the same as N/m2. dripping
dipping
sagging

viscosity [Pas]
mixing brushing
F N
Shear stress (t): = = Pa spraying
grinding
A m2
spattering printing

The shear rate () or velocity gradient is 103 102 101 100 101 102 103 104 105
obtained from the velocity v [m/s] and shear rate [1/s]
the plate separation h [m]. The units are
second-1. Figure 2: Effect of shear rate on applicational properties

.
Shear rate () =
v -1
[s ]
h
surface it should assume a high viscosity If the viscosity of a substance is constant
to prevent sagging on vertical substrates. at different shear rates, it is said to exhibit
Although the term viscosity is often used The flow behavior of paints under typical ideal or Newtonian behavior. Newtonian
in connection with coatings, the term processing conditions can be ordered flow is generally found only with low
flow behavior would surely be better. according to shear rate. molecular weight liquids such as water,
Usually coatings show a flow behavior in solvents and mineral oils. In practice,
which they become thinner, that is to say, Viscosity describes the frictional forces in most shearable systems have flow proper-
the viscosity value drops under the influ- a system and thus the resistance of a ties which depend on the shear rate.
ence of shear forces. This phenomenon, liquid to flow. The viscosity is a measure
known as pseudoplasticity, will be dealt of the viscous flow of a liquid. The larger If the viscosity decreases with increasing
with in more detail later. the viscosity, the less flowable the liquid. shear stress, the flow behavior is said to
The (shear) viscosity (dynamic viscosity) be intrinsically viscous, shear thinning or
Applicational properties of coatings are is obtained as the ratio of shear stress t to pseudoplastic. Most coatings and polymer
associated with different shear rates (fig. shear rate . The units are Pa s-1. solutions show pseudoplastic behavior.
2). When stirring (dispersing), low vis-
cosities are necessary but storage should Bingham fluids are viscoplastic but their
preferably take place at high viscosity so Viscosity flow properties are linear. After a mini-
that the pigments are prevented from mum shear stress, they reach the yield
settling out. For spray application, the point, tf , and begin to flow. Below this
paint should have as low a viscosity as point they behave as an elastic body.
possible but as soon as the paint is on the Examples are ketchup and certain wall

page 98 Technical Background_Rheological Additives


Flow curve Viscosity curve
a) Newtonian behavior
c b) pseudoplastic (non-Newto-
d d nian) behavior
c) Bingham behavior with yield
f
point tf
a c d) dilatant behavior

a
b
b

. .

Figure 3 Figure 4

paints. These liquids only begin to flow Flow behavior can be shown diagramma Examples of organic thickeners for sol-
when a particular stress is reached. This tically in two ways: as a flow curve or a ventborne or waterborne systems
occurs, for example, if a loaded paint viscosity curve.A flow curve shows the include:
roller is pressed against a wall and rolled. dependence of shear force t on shear polyureas
At that moment, the shear force is suffi- rate (fig. 3) and a viscosity curve shows cellulose derivatives
cient for the paint to become liquid and how the viscosity depends on the shear polyamides
wet the wall. As long as the paint is on rate (fig. 4).
the roller without any force applied it Examples of organic thickeners for water-
behaves like an elastic solid and does not Rheological additives can be roughly borne coatings include:
drip from the roller. separated into inorganic and organic associative thickeners
thickeners or thickeners for solventborne non-associative thickeners
Materials whose viscosity increases with or waterborne coatings.
increasing shear stress are shear-thicken- This list is not intended to be comprehen-
ing or dilatant. Dilatant behavior is shown Examples of modified inorganic thicken- sive.
by, for example, dispersions with high ers for solventborne and waterborne sys-
solids content or high polymer concentra- tems include: Associative thickening involves non-spe-
tions. Shear-thickening behavior is not bentonite cific interactions of hydrophobic end-
usually found in paints and coatings as it synthetic lattice-layer silicate groups of a thickener molecule both with
can lead to problems with processes pyrogenic silica (sometimes organically themselves and with components of the
involving pumping or stirring. modified) coating. The thickener produces a rever
sible, dynamic network of thickener mole-
cules and other components of the coat-
ing. The thickening effect is caused by
interactions of the hydrophobic end
groups of the thickener with other com-
ponents of the formulation.

Technical Background_Rheological Additives page 99


Non-associative thickening is thickening Associative thickening can produce rheo Polyurethane thickeners belong to the
by an entanglement of water-soluble, logy ranging from Newtonian to pseudo- associative category. The molecular
high molecular weight polymer chains. plastic. Associative thickeners are often weight of polyurethane thickeners is from
The effectiveness of a thickener is mainly used to adjust application properties such one to several powers of 10 lower than
determined by the molecular weight of as spattering or brushing resistance. For- that of non-associative thickeners. Non-
the polymer. Formulations thickened non- mulations with associative thickeners associative thickening can therefore be
associatively have pseudoplastic rheology often exhibit high gloss and good leveling. ignored.
with highly elastic properties. This pro-
duces good stabilization against settling
out and low sagging even with high build
coatings. Non-associatively thickened sys-
tems often have limited flowability. The
high molecular weight of the thickeners
can sometimes lead to compatibility prob-
lems such as depletion flocculation Chemistry of polyurethane thickeners
Associative thickeners also consist of
hydrophilic water-soluble or water-emul- Polyurethane thickeners are water-soluble or water-emulsifiable
sifiable polymer components and can polymers with a segmented structure. The middle section con-
simultaneously act in a non-associative sists of one or more hydrophilic segments while the end-groups
manner. Both thickening modes are are hydrophobic. Linking of the middle segments with each
exhibited by associative thickeners, albeit other and with the end-groups occurs mainly via free hydroxyl
to different extents. Table 1 shows thick- groups of the segments with mono- or poly-isocyanates forming
eners commonly used for waterborne the urethane structures which give their name to this class of
coatings and the way in which the thick- products. The molecular weights of typical polyurethane thick-
ening is produced. eners lie between 15,000 and 100,000 g/mol.

Overview of different classes of thickener and the method by which they thicken

Thickener Associative thickening Non-associative thickening

Polyurethane thickeners HEUR yes negligible

Polyacrylate thickeners no yes

Hydrophobically-modified polyacrylate thickeners HASE yes yes

Hydrophobically-modified polyether thickeners HMPE yes

Cellulose ethers no yes

Hydrophobically-modified cellulose ethers HMHEC yes yes

HEUR: Hydrophobically modified Ethylenoxide Urethane Rheology modifier Table 1


HASE: Hydrophobically modified Alkali Swellable Emulsion
HMPE: Hydrophobically Modified PolyEther
HMHEC: Hydrophobically Modified Hydroxy Ethyl Cellulose

page 100 Technical Background_Rheological Additives


Polyurethane chemistry opens up many the applicational properties of the thick- Although the simplified model in fig. 5 is
possibilities for synthesizing thickeners ener. A suitable choice of emulsifier helpful in explaining associative thicken-
with differing property profiles. allows the property profile of the thick- ing clearly, the actual mechanisms of
ener to be adjusted. thickening by polyurethane thickeners
This can be achieved by, for example, are more complex.
varying:
the type of hydrophobic end group Mode of action of polyurethane Investigations on solutions of polyur
the molecular weight of the thickener thickeners ethane thickeners in water show that the
the hydrophilic character of the middle thickener molecules are present in mono-
section by the choice of isocyanate and The associative thickening action of poly- molecular form only in highly diluted
the molecular weight of the poly urethane thickeners can be explained as solutions. With increasing concentration,
ethylene glycol follows: interactions of the thickener mole- the thickener molecules associate with
the middle section with hydrophobic cules with each other and with the surface each other to form loop micelles. The
dialcohols of dispersion and pigment particles pro- block-like structure of the thickener
the branching of the thickener mole- duce a network (fig. 5). favors this phenomenon:
cule by reaction with polyisocyanates
or polyalcohols
the branching of the middle section by
reaction with alkyl epoxides during
manufacture of the polyethylene glycol

Further variations are possible during the


formulation of the thickener as a water-
borne preparation. Substances high in
hydrophobic components require emulsi-
fiers or solvents as formulation aids. The
structure of the emulsifier co-determines
Figure 5: Mode of
action of polyur
ethane thickeners

Technical Background_Rheological Additives page 101


Figure 6: Bridging

emulsion particle hydrophobic


endgroup
monomolecular
flower-micelle dissolved thickener hydrophilic
middle segment

Figure 7: Entanglement Figure 8: Associative thickening via thickener gel

the hydrophobic components of the mole- In paints, polyurethane thickeners are The strength of the network and the
cule orient towards the interior of the usually used at concentrations at which resultant rheological properties of the
micelle, the hydrophilic middle segments two-phase systems have been observed in system can be controlled via the hydro-
form the outer loop-shaped sheath. aqueous solutions. It is therefore probable phobicity of the end groups. Long hydro-
that the polyurethane thickener is also phobic end groups exert strong interac-
At even higher concentrations, mutual present in paints as a two-phase system. tions and ensure efficient thickening. To
interaction of the loop micelles results in The thickener gel interacts via the hydro- achieve comparable thickening with
two phase systems consisting of a free- phobic groups with the surfaces of the shorter end groups, significantly higher
flowing phase with low thickener content pigments and binders. A refined model of concentrations are required.
and a thickener gel. In the free flowing the mechanism of associative thickening
phase, the thickener molecules are dis- by polyurethane thickeners is shown in The length of the hydrophobic group
solved individually or are present as loop fig. 8. influences not only the strength of the
micelles. The thickener gel consists of associative effect but also the kinetics of
associates of thickener molecules. The Polyurethane thickeners form a temporary exchange and thus the rate at which the
cohesion of the gels is thought to stem network. The linkage points of the net- associative linkage points break and
from bridging and entanglement mecha- work consist of thickener molecules and reform. When shear stress is applied to
nisms by the micelles (fig. 6 and 7). thickener micelles adsorbed on the pig- paints, the associative linkage points are
ment or binder surfaces. It is characteristic broken. If the thickener is unable to
If the concentration of thickener in aque- that the linkage points of the network are reestablish the disrupted linkage points
ous solution is raised still further, the two constantly breaking and reforming. The immediately, the associative network is
phase system changes into a single phase system is thus highly fluid which explains weakened. There is then a shear-rate-
thickener gel. the good flow and leveling characteristics dependent loss in viscosity.
of associatively-thickened paints.

page 102 Technical Background_Rheological Additives


Figure 9: Example for an absolute viscometer and various measuring cells

Long hydrophobic end groups possess a Measuring viscosity with the relative Leveling
slow rate of exchange; i.e. the viscosity of viscometer
thickeners with long hydrophobic end Leveling, the flow behavior in a horizontal
groups diminishes slowly under shear The volume of the sample is unknown; position, is determined with a leveling
stress. The formulation becomes pseudo- shear rate and shear stress cannot be doctor blade. In this method, the coating
plastic. Short hydrophobic end groups quantified. Relative viscometers are suit- is applied as five double lines with
exhibit a fast rate of exchange so that able for comparative measurements of increasing film thickness from 100 to
thickeners with such groups are effective systems with similar rheology. In the coat- 1000 m on a Leneta sheet. The propor-
even at high shear rates and result in for- ings industry, relative viscometers of the tion of lines which have coalesced is
mulations with Newtonian rheology. Brookfield or Stormer spindle type are quoted according to a scale of 0 (no level-
commonly used, usually at constant shear ing) to 10 (very good leveling). It is also
force. common practice to visually compare a

Test methods dried paint film with a standard (fig. 10).


The paint is usually applied in a manner
resembling subsequent application condi-
Measuring viscosity with the absolute tions.
viscometer

In absolute viscometers, the geometry of


the measuring cell is known and the shear
surface and plate separation are therefore
also known. The shear stress, shear rate,
and thus the viscosity can be calculated
from the shear force and speed. The abso-
lute viscometer is usually used to take
measurements over a range of shear rates.
The results are presented in flow curves
or viscosity curves. Typical absolute vis-
cometers are cone and plate or two-plate
rotational viscometers (fig. 9).

Figure 10: Bad and good flow after brush application

Technical Background_Rheological Additives page 103


Sagging Spattering characteristics areas of application are architectural
coatings, wood finishes, printing inks
Sagging, the flow behavior in a vertical The spattering characteristics can be and leather coatings.
position, is determined with a sagging determined by applying a specified
doctor blade. Ten stripes of the paint are amount of paint uniformly on a previously Can all TEGO ViscoPlus types be com-
applied using the doctor blade in thick- conditioned roller and rolled several times bined with each other?
nesses of 75 to 300 m on a Leneta over a grid. The paint spray thrown from All TEGO ViscoPlus types can be com-
sheet. Immediately after application, the the roller is collected on a black card bined with each other. If the required
card is lifted into a vertical position so that under the grid. The test card is compared rheology cannot be achieved with one
the stripes lie parallel to the horizontal. with a standard tested at the same time. thickener, a combination of types with
The stripes with the lowest film thickness differing rheology profiles is recom-
are at the top. After drying, the stripe at These test methods are shown in a video mended.
which the paint starts to sag is given on a on our Homepage entitled Various meth-
scale of 0 to 10: 0 meaning that all stripes ods for measuring viscosity. How can a rheology profile be finely
sagged and 10 meaning that no stripes adjusted?
sagged (fig. 11). If the required rheology profile cannot
be achieved with one thickener, several
Alternatively, it is possible to determine thickeners can be combined. All TEGO
at which film thickness sagging starts to
occur by applying the paint, in various
FAQs ViscoPlus types can be combined with
each other. The rheology of the combina-
thicknesses or as a wedge, to a vertical tion always lies between the profiles of
surface. For which paint formulations is TEGO the types used.
ViscoPlus suitable?
TEGO ViscoPlus is only recommended Can I combine TEGO ViscoPlus with
Brushing resistance for thickening waterborne coatings. The thickeners which have a different chemi-
thickening effect is based on the interac- cal composition?
Brushing resistance is determined by tions of the additive with pigment and Basically, combinations with the polyacry-
applying a specified amount of paint to a binder particles. Thus, TEGO ViscoPlus late or cellulose ether thickeners com-
test surface and assessing the resistance can basically be used in all waterborne monly used in waterborne paints are pos-
felt on distributing the paint with a brush. emulsion paint formulations. The main sible. However it is recommended that

Figure 11:
Sagging test

page 104 Technical Background_Rheological Additives


the compatibility of the thickener in the What is the procedure if the rheology of Can a paint be made thixotropic using
formulation is checked. a paint needs to be set using a combina- TEGO ViscoPlus?
tion of thickeners with differing rheo At high shear, the static viscosity of the
How do the various TEGO ViscoPlus logy profiles? pseudoplastic TEGO ViscoPlus 3030
types differ? With a pseudoplastic thickener, the rheo and 3060 falls. After the shear force is
The thickeners differ in the rheology they logy should initially be adjusted to a speci- removed, the viscosity prior to shear is
produce in the application system: fied target value using low to medium spontaneously reinstated. Thixotropy, in
shear rates. A Newtonian thickener is the sense of time-delayed increase in
TEGO ViscoPlus Rheology then added until the desired viscosity is static viscosity, cannot be obtained with
TEGO ViscoPlus 3000 Newtonian achieved at high shear rates. The Newto- TEGO ViscoPlus.
TEGO ViscoPlus 3010 Newtonian with nian thickener can also affect the viscosity
high thickening at low to medium shear rates which What are the ecological advantages of
at high shear should therefore be rechecked. If neces- TEGO ViscoPlus?
rates sary the dosage of pseudoplastic thickener All grades are free of volatile organic
TEGO ViscoPlus 3030 pseudoplastic must be further adjusted. compounds (VOC) and of alkylphenol
TEGO ViscoPlus 3060 strongly pseu- ethoxylates (APE). No organotin catalysts
doplastic Which types of binder can best be are used in their manufacture.
thickened with TEGO ViscoPlus?
What are the advantages of combining For a thickener network to form, the
TEGO ViscoPlus with polyacrylate thickener must associate with hydropho-
thickeners? bic surfaces. Effective thickening can be
Combination with polyacrylate thickeners obtained with emulsifier-stabilized emul-
enables the elastic viscosity of the paint to sions based on acrylates and styrene acry-
be increased. This leads to improved sta- lates. Thickening with hydrophilic vinyl-
bility against settling and better sagging acetate copolymers is less pronounced.
characteristics. Leveling is, however, fre-
quently impaired. Why does the PVC influence the thick-
ening effect of TEGO ViscoPlus?
What are the advantages of combining For a network to form, the thickener must
TEGO ViscoPlus with cellulose ethers? associate with the hydrophobic surface of Literature:
Edward J. Schaller, Peter R. Sperry
Combinations of cellulose ethers with the binder particles. In paints with a high Associative thickeners
Handbook of Coatings Additives, Vol. 2,
polyurethane thickeners are usually PVC, too few binder particles are avail- edited by Leonard J. Calbo, pp. 105-164
encountered in architectural coatings able to form a strong thickener network.
Johan Bieleman PUR-Verdicker
with a high PVC. The cellulose ether Johan Bieleman, Lackadditive, Wiley-VCH,
imparts water retention to the paint and How does the pH-value affect the thick- pp. 51-59

thus a sufficiently long open time. In addi- ening performance of TEGO ViscoPlus? Holger Reimann, Betina Joos-Mller,
Klaus Dirnberger und Claus D. Eisenbach
tion the elastic viscosity of the paint is In the typical range of pH for emulsion Assoziativverdickern auf der Spur
increased. Stability to settling and sagging paints, the pH does not affect the thicken- Farbe & Lack, 5/2002, pp. 44-55

characteristics are also improved. In many ing performance of TEGO ViscoPlus. Markus Schmidtchen, Thadeus Schauer,
cases, however leveling and gloss are Rolf Nothhelfer, Claus D. Eisenbach
Dem Netzwerk auf der Spur
impaired by the cellulose ether. Farbe & Lack, 2/2005, pp. 34-39

Technical Background_Rheological Additives page 105


Hydrophobing Agents
TEGO Phobe

Seite 106 Technischer Hintergrund_Hydrophobierungsmittel


Because of their pore and capillary struc-
ture, mineral building materials absorb
moisture on contact with water. This
often leads to visible and invisible damage
caused either by the water itself or by
processes in the walls which are initiated
or enhanced by water.

Examples of facade damage caused by


water are:
growth of algae, fungi or spores
Figure 1: Damage to facades caused by inadequate water vapor permeability
salt efflorescence
frost damage
loss of insulating effect
flaking off of coatings Hydrophobicity
An effective method of protecting walls Hydrophobic means water-hating. A sur- It can be determined by applying water
which are exposed to weathering is by face is described as hydrophobic if it is not droplets to the surface (fig. 2) and using
treating the surfaces with materials which or is not fully wetted by water droplets. contact-angle measuring equipment
are impenetrable to water or are water A parameter characterizing the hydropho- which measures the tangent at the sub-
repellent (hydrophobic materials). bicity of a surface is the contact angle. strate/liquid/air boundary. The result is
quoted as the interior angle of the liquid
droplet with the substrate. Surfaces with
contact angle greater than 90 degrees are
classified as hydrophobic. If the contact
angle is less than 90 degrees, they are said
Figure 2: Contact angle to be hydrophilic. A video Measurement
of contact angle can be found on our
air
homepage.
water-droplet

substrate
Contact angle of a water-droplet
on a hydrophobic surface

Technical Background_Hydrophobing Agents page 107


Chemistry of hydrophobing agents

Silicone-based hydrophobing agents Silicones have a very high spreadability;


they attach very readily to surfaces. The
Chemistry of silicone products hydrophobic effect involves orientation to
The fundamental building blocks of sili- the wetted surface. The oxygen atoms of
cones are chlorosilanes, produced by the the siloxane chain orient themselves to
Rochow synthesis method, which are the surface while the alkyl (usually
condensed to higher siloxanes by hydroly- methyl) groups point away from the sur-
sis or alcoholysis. The number of chlorine face thus producing a hydrophobic sur-
substituents gives the number of valences face (fig. 3). The ability of silicones to
available for condensation. Chlorosilanes bond via Si-O-Si links to siliceous sur-
are classified into four types depending faces gives a system which is long-lasting.
on their degree of chlorination.

Designation Abbreviation Reactivity Siliconates


Monochlorosilane M 1
Dichlorosilane D 2 Siliconates are highly alkaline solutions.
Trichlorosilane T 3 After application, they initially react with
Quatrochlorosilane Q 4 atmospheric carbon dioxide (CO2) to form
silanols which then react together to pro-
Different types of silicone hydrophobing duce a silicone resin. Methyl- or propyl-
agents are obtained depending on the potassium silicates are used almost exclu-
types of units reacting together. sively. Reaction with CO2 also produces
potassium carbonate as a by-product
which is deposited as a salt on the surface.
Because the potassium carbonate formed
Figure 3: Activity of silicones on mineral substrates is water soluble, siliconates are used for
interior use, e.g. for hydrophobing plas-
CH3 CH3 CH3 CH3 CH3 CH3 CH3 CH3 CH3 CH3 terboard.

Si Si Si Si Si

O O O O
substrate

page 108 Technical Background_Hydrophobing Agents


Silanes Silanes are mainly used for hydrophobing Polydimethylsiloxanes
mineral building materials. A distinction
Silanes are used for hydrophobing mineral is made between internal hydrophobing Polydimethylsiloxanes are higher molecu-
materials. Silanes are manufactured by in which the silane is added to the build- lar weight linear condensation products
reacting chlorosilanes with alcohol, usu- ing material, e.g. concrete, and external of D- and M-units. They have a lower
ally methanol or ethanol. The low molec- hydrophobing in which it is applied in a penetrating power than oligomeric silox-
ular weight of silanes is both an advantage subsequent step by impregnation. anes. Polydimethylsiloxanes are mainly
and a disadvantage. Compared with used as hydrophobing agents in coatings
higher molecular weight silicones, they and plasters, for example in silicate paints,
are much smaller and can therefore pene- Oligomeric Siloxanes siloxane-modified coatings. Amino-modi-
trate noticeably better. The disadvantage fied polysiloxanes in these formulations
is their high volatility and the associated Self condensation of chlorosilanes pro- produce good hydrophobing combined
possible loss during application. duces reactive low-molecular weight with a high water-beading effect.
(oligomeric) siloxanes which are used for
Upon curing, a silane reacts first with hydrophobing mineral surfaces. As with
moisture from the air or the building silanes, oligomeric siloxanes have a high Silicone resins
material to give a silanol which, in a sub- penetrating power. However, compared
sequent condensation step, crosslinks with the silanes, they have the advantage The use of hydrophobing agents based
with itself and the substrate. The speed of a low vapor pressure and, therefore, do on silicone resins gives rise to the names
of the condensation reaction of silanes is not evaporate. Analogously to the silanes, silicone resin paints and silicone resin
strongly affected by the temperature and oligomeric siloxanes can be further cross- plasters. Compared with organic resin
alkalinity of the substrate. Higher temper- linked by condensation reactions. They binders silicone resins have a relatively
atures and high pH favor the condensation are mainly used as internal or external low molecular weight of between 2,000
reaction. Among the alkoxysilanes, types hydrophobing agents for mineral building and 3,000 g/mol. The residual reactivity
with methyl groups have the highest reac- materials. in the resin enables the resin to crosslink
tivity. As methanol is formed as a by- by a condensation reaction. The water
product of the reaction, the more inert repellant effect is already fully developed
ethoxysilanes are increasingly used. The immediately after drying. Silicone resins
reaction of the silane can be accelerated are also used as hydrophobing agents in
by suitable catalysis. silicone-silicate formulations.

Technical Background_Hydrophobing Agents page 109


Waxes Formulation concepts for exterior coatings
Waxes both as dispersions in organic sol-
vents and as aqueous emulsions have lim-
ited penetrating power. Hydrophobing Facade protection theory 1.Protection of the facade from direct
with waxes is therefore mainly a surface ingress of water through the facade
effect. As a result of this, hydrophobing The protection of a facade against mois- surface (Permeability for water to
with waxes is of limited durability as the ture by appropriate treatment is a very DIN EN 1062-3).
wax layer is eroded by the effects of important factor for maintaining a build- 2.Maintenance of the porous structure
water and weathering. Additionally, the ing. At first sight, sealing the facade with of the facade thus allowing a moist or
thermoplasticity of the waxes leads to a a waterproof coating seems to be the best wet wall to dry. (Water vapor trans-
higher dirt uptake by the surfaces. solution to protect surfaces against mois- mission rate to EN ISO 7783).
ture. On closer consideration, however, it
is apparent that there are numerous ori-
Polyfluorocarbon compounds gins of water in a facade. Water permeability, w-value
(EN ISO 1062-3)
Surfaces treated with polyfluorocarbon For example, cracks or other defects in
compounds are particularly hydrophobic the coating of the facade, rising moisture, The water permeability, often called cap-
and also have oil repelling (oleophobic) damage in roof drainage or dampness illary water absorption, describes the
properties. The high cost of these prod- from the interior contribute to entry of amount of water which can be absorbed
ucts and their poor biodegradability limits moisture and transport of salts into the by capillary suction by a square meter of
their use to special niche applications. masonry. It is important for a facade to building material within a certain time
have functioning moisture management. interval. In EN ISO 1062-1, there are
This involves two parameters which can three classes of capillary water uptake.
be measured by standardized methods: Building materials in the best (class 3)
have a maximum of 0.490 kg capillary
water uptake on one square meter in 24
hours.

page 110 Technical Background_Hydrophobing Agents


Water permeability classes, w-value, Water vapor transmission rate, sd-value
(EN ISO 1062-1) (EN ISO 1062-1)

Class Water uptake w-value Class Water vapor diffusion sd-value

III low < 0.1 I high < 0.14

II medium 0.1 0.5 II medium 0.14 1.40

I high > 0.5 III low > 1.40

Water vapor transmission rate (perme- w-value and sd-value is at the most other. The yellow area shows the region
ability) (V-value or sd-value) 0.1 kg/(m h). Ideally formulated paints in which the product of w- and sd-values
have a low capillary water uptake (class 3) is 0.1 kg/(m h) or smaller. The extent
The water vapor transmission rate is and very high water vapor transmission to which individual facade coating sys-
determined by EN ISO 7783. The V-value rate, characterized by a low sd-value in tems fulfill this condition is shown by the
describes the amount of water vapor in class 1. Figure 4 shows quantitatively the colored areas.
grams which can diffuse in one day from a relationship of w- and sd-values to each
coating area of one square meter. More
often than the water vapor transmission
rate, the diffusion equivalent thickness
of air (sd-value) is given. The sd-value, Figure 4: Facade protection theory according to Knzel

which can be calculated from the V-value, class 3 class 2 class 1


describes the thickness of an imaginary
Sd-value
layer of still air which has the same resis- in m
tance to water vapor diffusion as the coat- solventborne paints
ing. EN 1062-1 divides the sd-value into 2
three classes. Coatings with an sd-value
less than 0.14 m are assigned to the best emulsion paints class 3
class (class 1) and have very good water
silicone resin paints
vapor transmission.
1
silicate emulsion paints
The relationship of these parameters to class 2
each other is given in Knzels facade the- silicate paints
ory. Optimally formulated facade coatings
have coordinated w- and sd-values and
class 1
will lose water as water vapor can be 0
0 0.1 0.2 0.3 0.4 0.5
taken up faster than rain. This property is w-value in kg/m 2 x h
fulfilled by paints where the product of

Technical Background_Hydrophobing Agents page 111


Formulation of paints which satisfy the requirements of
Knzels facade protection theory

The most important parameter affecting called formulations with low PVC or
w- and sd-values is the pigment volume strongly bound formulations. Clear
concentration (PVC). The pigment vol- coats have, according to the formula, a
ume concentration describes the volume PVC of zero and theoretically a paint
ratio of the powder-form pigments and formulated with no binder has a PVC of
filler to the total including the binder in 100%. In practice, paints are found with
the dried coating film. It is calculated from extremely low amounts of binder up to
the following formula. a PVC of 90 to 95%.

VPigments + VFillers If the PVC of a formulation is altered step-


PVC = 100% wise over the complete PVC range, a PVC
VPigments + VFillers + VBinders
range is reached in which the film has a
high tension. This can lead to cracks in
The PVC for a formulation with a small the coating. That point is known as the
amount of binder and thus a correspond- critical PVC, and in this region the paint
ingly large proportion of pigments and undergoes a change between a binder
fillers is a high value. Such formulations excess at low PVC to binder deficiency at
are indicated by the terms formulations high PVC. Paints with binder excess at
with high PVC or (because of the small low PVC are termed sub-critically formu-
amount of binder) weakly bound formu- lated. This means that the formulation
lations. Conversely, formulations with a contains an excess of binder which will fill
high proportion of binder and low all cavities between pigments and fillers.
amounts of pigments and fillers are

page 112 Technical Background_Hydrophobing Agents


In contrast, super-critically formulated Neither super-critical formulation nor
paints with high PVC are binder-deficient. sub-critical formulation can give low
That means that in super-critically formu- water uptake and high water vapor trans-
lated paints, the pigments and fillers are mission. Only formulations with hydro-
not completely wet out by the binder and phobing agents simultaneously offer very
cavities are formed. Super-critically for- good water permeability and water vapor
mulated paints are therefore often termed transmission rates. The various formula-
open pored. tion concepts and coating types are
described below.
Sub-critical formulations have very good
water permeability characteristics
(w-value). The binder excess and corre-
sponding continuous film provides pro-
tection against water penetration. How-
ever the film strongly reduces the water
Formulation concepts for facade
vapor transmission rate which leads to paints and plasters
high sd-values. In practice, too low a
water vapor transmission rate can allow
the evaporating moisture from the walls Silicone resin paints and plasters
to produce a water vapor pressure under
the coating which can cause defects in the The best protection for facades is offered by paints with low water
coating such as blistering. uptake and good water vapor transmission. For this, silicone resin
paints and plasters offer advantages over emulsion paints and plas-
In contrast, super-critically formulated, ters, as they satisfy both requirements. Silicone resin paints and plas-
open-pore coatings have very good water ters are super-critically formulated, i.e. with high PVC. The resulting
vapor transmission rates. However, their open microporous structure produces excellent water vapor transmis-
porosity leads at the same time to high sion allowing wet walls to dry out. This avoids damage to buildings
capillary water uptake which means that such as loss of insulating effect, attack by mold or damage to the
super-critical formulations do not offer paint by blistering or flaking. Dry masonry is also an effective con-
adequate protection from the moisture. tributor to a healthy and pleasant indoor environment.

Technical Background_Hydrophobing Agents page 113


Guiding formulation for silicone resin paint

Item Component Amount by weight Ingredient/Effect

1 Water 28.75

2 Walocel XM 6000 PV 0.30 Cellulose thickener TEGO Phobe 1650 effectively prevent
capillary water uptake by the coated
3 TEGO Foamex 855 0.20 Defoamer
masonry. Further advantages of TEGO
4 ActicidE MBS 0.15 Biocide Phobe 1650 include its high effectiveness
5 Calgon N new 0.05 Wetting and dispersing additive in small amounts, excellent early water
6 TEGO Dispers 715 W 0.30 Wetting and dispersing additive resistance and low dirt pick-up by the
coating. Addition of the polysiloxane
7 AMP90 0.10 Neutralizing agent
TEGO Phobe 1401 or TEGO Phobe
8 Kronos 2310 12.50 Titanium dioxide 1505 produces an additional water bead-
9 Socal P 3 10.00 Calcium carbonate, precipitated ing effect. For this, an added quantity of
10 Omyacarb 5 15.00 Calcium carbonate 1 to 2% is recommended.

11 Omyacarb 2 10.00 Calcium carbonate


According to European Standard (EN
12 Aica TG 3.00 Mica 1062-1),+ facade coatings are grouped
13 Sipernat 820 A 2.00 Aluminum silicate according to their w-values (EN 1062-3)
14 TEGO Phobe 1650 4.00 Hydrophobing additive and sd-values (EN ISO 7783-2) each into
three classes. With silicone resin paints,
15 Dowanol DPnB 1.00 Coalescing agent
the highest demands can be achieved with
16 Acronal S 790 12.00 Styrene acrylate binder w-value in class 3 (lowest water uptake)
17 TEGO ViscoPlus 3000 0.65 Polyurethane thickener and sd-value in class 1 (highest water
100.00 vapor permeability).

Exterior coatings based on nanohybrid


binders

The addition of silicone resin emulsions Hybrid binders of an acrylate dispersion


produces protection against water, for and an amorphous silica are relatively new
example, driving rain. The silicone resin commercial products. These binders allow
coats the open pores without closing paints to be formulated which, despite
them. Thus water vapor transmission is having a high binder content, are more
preserved but the hydrophobic coating open to water vapor transmission than
efficiently prevents water from penetrat- similar coatings based on pure polymer
ing into the pores. binders, that is with lower PVC. Com-
pared with conventional dispersions,
Silicone resin coatings offer the most nanohybrid binders have the advantage
effective protection for buildings. TEGO that the amorphous silica imparts thermo-
Phobe 1650 is one of the newest genera- plasticity to the coating film and makes it
tions of silicone resin hydrophobing addi- less susceptible to dirt pick up. Formulat-
tives. Formulations incorporating the ing silicone resin paints with nanohybrid
waterborne silicone resin emulsion dispersions combines the low dirt pick-up

page 114 Technical Background_Hydrophobing Agents


Guiding formulation for a silicone resin paint based on nanohybrid dispersion

Item Component Amount by weight Ingredient/Effect

1 Water 14.8
of the latter with the good properties of 2 Tylose MH 30000 YP2 0.2 Cellulose thickener
the former. A three-fold combination of a
3 TEGO Foamex 855 0.3 Defoamer
conventional binder with a nanohybrid
dispersion and the silicone resin TEGO 4 ActicidE MBS 0.4 Biocide

Phobe 1650 has proved particularly 5 Dowanol DPnB 3.2 Coalescing agent
effective. 6 TEGO Dispers 755 W 1.3 Wetting and dispersing additive

7 AMP90 0.4 Neutralizing agent

Siloxane facade paint with water- 8 Kronos 2190 22.5 Titanium dioxide

beading effect 9 Omyacarb 5 GU 6.0 Calcium carbonate

10 Omyacarb 2 GU 6.0 Calcium carbonate


Since the end of the 1990s, facade paints
11 AICA TG 4.0 Mica
with marked water beading effect have
become established. Such coatings are 12 Sipernat 820 A 3.2 Aluminum silicate

characterized by a very strong water- 13 TEGO Phobe 1650 7.5 Hydrophobing additive
beading effect with a contact angle 14 Col.9 DS 1200 X 15.0 Nanohybrid binder
between water/coating of more than
15 Acronal A 684 10.5 Acrylate binder
140. This is often associated with a low
16 Collacral LR 8990 2.7 Polyurethane thickener
dirt pick-up as well as a self-cleaning (1:1 in Water)
effect. Experience in various regions of
17 TEGO Foamex 855 0.4 Defoamer
the world has shown that environmental
influences such as air pollution, climate or 18 ActicidE MKB 1.6 Film preserving agent

type and frequency of rain have a decisive 100.00


effect on self-cleaning ability.

The water-beading effect is obtained by


Guiding formulation for a siloxane coating with water-beading effect
using a special hydrophobing additive,
TEGO Phobe 1505, and a special surface Item Component Amount by weight Ingredient/Effect
texture of the coating. This desired
1 Water 29.70
micropimple structure is obtained by
using highly crystalline quartz or calcium 2 TEGO Foamex 825 0.10 Defoamer

carbonate filler with a particle size 3 Surfynol E 104 0.25 Wetting and dispersing additive
between 15 and 20 micrometers and a 4 Walocel XM 6000 PV 0.30 Cellulose thickener
narrow particle size distribution. Surface-
5 ActicidE MBS 0.10 Biocide
active water-soluble materials in the coat-
ing reduce the water-beading effect and, 6 Kronos 2044 20.00 Titanium dioxide

in choosing raw materials, care must be Sibelite M 3000 or 32.00 Quartz


taken to ensure that they are low in sur- 7 Calcimatt Calcium carbonate

factant. As with silicone resin paints, 8 Ammonia 25 % 0.15 Neutralizing agent


siloxane paints have very low water 9 TEGO Phobe 1505 2.40 Hydrophobing additive
uptake and excellent water vapor trans-
10 Acronal S 790 15.00 Styrene acrylate binder
mission.
100.00

Technical Background_Hydrophobing Agents page 115


Guiding formulation for a dispersion silicate paint Silicate paints and plasters

Item Component Amount by weight Ingredient/Effect Silicate paints and plasters contain water
1 Water 22.30 glass, usually in combination with poly-
2 Betolin V 30 0.10 Thickener mer dispersions as binders. The ability of
water glass to react with silicate sub-
3 TEGO Dispers 735 W 0.30 Wetting and dispersing additive
strates and form a strong chemical bond
4 Betolin Q 40 0.30 Stabilizer makes silicate systems very attractive for
5 TEGO Foamex 825 0.20 Defoamer coating the most common mineral sub-
6 Natrosol 250 HHR 0.30 Cellulose thickener strates found outdoors. This property,
known as silicification, makes silicate
7 Kronos 2310 10.00 Titanium dioxide
paints very durable. The high proportion
8 Omyacarb 5 30.00 Calcium carbonate of inorganic components gives the silici-
9 Plastorit 000 5.00 Talc fied coating a mineral appearance and
10 TEGO Phobe 1401 4.00 Hydrophobing additive excellent water vapor transmission. A
disadvantage however is the high capillary
11 Acronal S 559 6.00 Styrene acrylic binder
water uptake of such formulations. This
12 White spirit 1.50 Coalescing agent can be reduced by using hydrophobing
13 Betolin K 28 20.00 Potassium water glass binder agents specially suited to silicate paints,
100.00 for example TEGO Phobe 1505 or 1401.

Silicone-silicate paints
Guiding formulation for a silicone-silicate paint
These are a variant of silicate paints in
Item Component Amount by weight Ingredient/Effect which the binder is a three-fold combina-
1 Water 22.30 tion of emulsion, silicone resin and water
2 Betolin V 30 0.10 Thickener glass. In terms of values for capillary
water uptake and water vapor diffusion,
3 TEGO Dispers 715 W 0.30 Wetting and dispersing additive
they are similar to other silicate paints
4 Betolin Q 40 0.30 Stabilizer but have the advantage of lower dirt
5 TEGO Foamex 825 0.20 Defoamer pick-up.
6 Natrosol 250 HHR 0.30 Cellulose thickener

7 Kronos 2310 10.00 Titanium dioxide

8 Omyacarb 5 30.00 Calcium carbonate

9 Plastorit 000 5.00 Talc

10 TEGO Phobe 1650 4.00 Hydrophobing additive

11 Acronal S 559 6.00 Styrene acrylic binder

12 White spirit 1.50 Coalescing agent

13 Betolin K 28 20.00 Potassium water glass binder

100.00

page 116 Technical Background_Hydrophobing Agents


Emulsion paints with silicate character Guiding formulation for a dispersion paint with silicate character

Because of their formulation with quartz Item Component Amount by weight Ingredient/Effect

flour or other mineral fillers, emulsion 1 Water 14.70


paints with silicate character are particu- 2 Tylose MHB 10.000 YP2 0.20 Cellulose thickener
larly open-pored or capillary active and
3 TEGO Dispers 715 W 0.30 Wetting and dispersing additive
thus permeable to water vapor.
4 TEGO Foamex 825 0.30 Defoamer

5 Kronos 2310 12.00 Titanium dioxide


Emulsion paints and plasters 6 Omyacarb 5 10.00 Calcium carbonate

7 Talkum AT 1 1.50 Talc


Using polymer dispersions as binders in
emulsion paints and plasters prevents 8 Sikron Feinstmehl SF 3000 35.00 Quartz

water uptake by the coating. If water 9 ActicidE MBS 0.20 Biocide


beading is needed, this can be achieved 10 TEGO Phobe 1401 2.50 Hydrophobing additive
by adding TEGO Phobe 1401 and
11 White spirit 0.80 Coalescing agent
TEGO Phobe 1500 N.
12 Dowanol DPnB 0.80 Coalescing agent

13 Desavin 0.70 Plasticizer

14 Acronal S 559 21.00 Styrene acrylate binder

100.00

Technical Background_Hydrophobing Agents page 117


Hydrophobing additive for impregnation
and primers

Impregnation is performed on building Primers are used to reduce the absor-


materials when it is not intended to coat bency and consolidate the substrate. For
them further. The aim of impregnation is this, the primer must be able to penetrate
to reduce the water uptake of a building the substrate adequately. Otherwise, too
material without otherwise altering its much material would remain on the sur-
characteristics such as porosity or appear- face and consolidation of the substrate
ance. The impregnating agent must not would not be sufficient. Adhesion prob-
impair water vapor and carbon dioxide lems might arise with subsequent coats.
permeability. Impregnation with siloxane The right primer can have a decisive influ-
products can be achieved with TEGO ence on the durability of the complete
Phobe 6010 for solvent-based impregna- coating system.
tion or TEGO Phobe 6510 and 6600 for
water-based impregnation. Impregnation Effective priming protects the coating
should not be used for materials which from infiltration of salts and water which
have little or no absorbency. can damage the building. If the top coat is
damaged, the primer must additionally
protect the building material from further
damage by water penetration.

With siloxanes of the TEGO Phobe 6xxx


Figure 5: Measuring of water absorption series, Evonik offers products for formu-
lating solvent- and water-borne primers.

Test blocks Water Test methods


PU-foam Bath
Determination of water vapor permea-
bility by the wet cup method

Evonik uses a gravimetric method from


EN ISO 7783-2 to determine the water
vapor permeability by comparison with an
inert carrier material. The substrates are
polyethylene frits with a diameter of 60
mm. The coating material is applied to the
frit with a flat brush in the amount per

page 118 Technical Background_Hydrophobing Agents


unit area recommended for use in prac-
tice. If details of the amount to be applied
for a given area are not available, Evonik
applies the paint in two coats using 400
ml/m in total. The coating is dried
overnight in a standard climate (23C, Wet-Cup Dry-Cup
50% relative humidity) followed by 24
hours at 50C.

A weighing dish with a diameter of 61 Coating


mm and height of 30 mm is filled with 20 Glass frit
100% relative 0% relative
ml of distilled water. A small sponge is humidity humidity
placed in the dish to stop the underside of
the frit coming into contact with liquid water Balance
glass
P2O5
which could otherwise invalidate the Climatic chamber: 23C / 50% relative humidity
measurement. The dish is closed with the
Figure 6: Wet-cup method
coated frit and the joint between the frit
and the weighing glass sealed with hot
melt adhesive. The whole is then weighed
accurately using an analytical balance to
0.1 mg and kept for five days in a cli-
mate chamber at 23C and 50% relative
humidity. After this, it is weighed again. and the glass is then kept in a standard cli- The correct amount of coating is then
By comparison with a non-coated speci- mate of 23C and 50% relative humidity. poured onto the block and distributed
men, the amount of water diffused is The water vapor diffusion is thus in the with a flat brush ensuring that the sides
determined from the weight loss of the opposite direction. are coated as well. The amount of coating
sample (fig. 6). The performance of the material is based on the recommended
test can be seen on our internet site under Comparison of wet- and dry-cup methods amount used in practice. If there are no
Measurement of water vapor permeabil- has shown that the wet-cup method is recommendations as to the amount to be
ity (sd-value). more accurate. used for a given area, Evonik uses a total
of 400 ml/m applied in two coats. Care
must be taken to ensure that all the pores
Determination of water vapor permea- Measurement of capillary water uptake of the block are closed. The coated block
bility by the dry cup method is kept overnight in a standard climate
The capillary water uptake is measured (23C, 50% relative humidity) followed
The dry-cup method is another way of by Evonik from EN 1062-3. The test by drying for 24 hours at 50C.
measuring the water vapor permeability. specimens are calcium sandstone blocks
Preparation of the sample is the same as with an area of 115 x 70 mm = 0.008 m2
that for the wet-cup method. However, in and a thickness of 20 mm. The blocks are
the dry cup method the weighing dish is prepared by scrubbing them free of dirt
filled with phosphorous pentoxide (P2O5) with water and then drying for 24 hours
to produce an internal humidity of 0% at 50C.

Technical Background_Hydrophobing Agents page 119


The test samples are placed on foam in a Determination of the contact angle
water-filled tray (fig. 5). The level of the
water must reach the underside of the The contact angle describes the wettabil-
samples and from time to time the water ity of a substrate by a liquid, predomi-
level is checked and water replenished if nantly water in the case of exterior paints.
necessary. After 24 hours, the blocks are To determine the contact angle, a water
removed from the water bath, placed on droplet with a specified volume is placed
paper, blotted and weighed. DIN EN on the coating. Using an optical method,
1062-3 specifies a fourfold watering of the angle of the tangent of the drop to the
the block. In the first watering, water-sol- substrate is measured. High contact
uble components of the coating are angles indicate poor wetting and conse-
washed out. For classification of EN ISO quently good water beading. In contrast,
1063-1, the result of the fourth watering low contact angles indicate good wetting
is taken and specified as the w24-value, and poor water beading. The contact
e.g. w24 = 0.5 kg/(m2 h) angle can change during the course of the
measurement. In particular, with fresh
The method of measuring the capillary paints which have not been exposed to
water uptake can also be seen on our water or weathering, the contact angle
internet site. decreases during the course of the mea-

page 120 Technical Background_Hydrophobing Agents


surement. The reason for this is that Dirt pick-up tains both organic and inorganic matter
emulsifiers and other water-soluble com- such as would typically be found in highly
ponents are dissolved out of the paint film In addition to the technical properties of a polluted urban or industrial areas. The
and these lower the interfacial tension of coating, it is also important that it retains results of the soiling test are specified as
the water droplet. If the coating is irri- its appearance over a long period of use. delta L of the sample before and after the
gated for 24 hours prior to the measure- One obvious visible aspect of an exterior test. Experience shows that this soiling
ment, higher and more stable values of coating is its soiling characteristics. This test produces results which would other-
the contact angle are obtained. When can be tested in several years of outdoor wise only be obtained by several years of
comparing results of contact angle mea- weathering but the tendency of an exter- outdoor weathering tests.
surements, it is therefore always neces- nal coating to soil can be simulated in a
sary to know details of the pre-treatment. fast test developed by Evonik. Using a
converted washing machine, test samples
No statements about the capillary water of coatings are sprayed with a dirt disper-
uptake can be made from the contact sion and then dried. This is repeated sev-
angle of a coating. eral times. The dirt dispersion used con-

Determination of the contact angle using an optical method.

Technical Background_Hydrophobing Agents page 121


FAQs

Vertical tracks which differ from the We have found that our silicone resin
original color are caused by rain. How paints show a strong increase in viscosity
can this sensitivity to sudden rain of a after storing for 5 to 6 months. How can
recently applied silicone resin paint be we prevent this?
improved? The order of addition during the manu-
We offer TEGO Phobe 1650, a silicone facture of the paint plays an important
resin with early water resistance. That role. After manufacturing the millbase,
means that the hydrophobic effect of the silicone resin emulsion should be
TEGO Phobe 1650 develops very added first and the binder dispersion
quickly after application. According to the only added after further stirring.
method for determination of capillary
water uptake, EN 1062-1, coatings must How much silicone resin do I need to
reach their full effectiveness after the formulate a silicone resin paint?
fourth exposure to water. TEGO Phobe There is no clear rule as to how much sili-
1650 actually achieves this after only two cone resin a formulation must contain.
exposures. More important than the quantity used is
that the formulation must fulfill the physi-
Does the silicone resin in silicone facade cal demands made on it, such that it
paints affect the sd value and is the PVC achieves class 3 in permeability of water
of the coating altered? and class 1 in water vapor transmission
The amount of silicone resin has practi- rate. Older formulations contain up to
cally no effect on the sd-value. Investiga- 10% silicone resin emulsion to satisfy
tions have shown that silicone resins do these demands. With the newest genera-
not behave like binders in their effect on tion of silicone resin emulsions, similar
wet abrasion resistance or sd-value. In cal- properties can be reached with only
culating the PVC, silicone resins should 4 to7%.
therefore not be incorporated into the
calculation as binders.

page 122 Technical Background_Hydrophobing Agents


In choosing the silicone resin, it should be (The abbreviations M-, D-, T- and Can I improve the wet abrasion resis-
noted that, by definition, silicone resin Q-units are explained in the section tance of a coating by using silicone
paints must be made hydrophobic with a Chemistry of silicone products in this hydrophobing additives?
silicone resin. Even if linear polysiloxanes chapter.) Investigations have shown that silicone
can produce a similar hydrophobing effect hydrophobing materials have only a slight
they cannot, by definition, be used to How is a silicone resin defined? effect on wet abrasion resistance.
hydrophobe silicone resin coatings. Silicone resins are silicone structures that
contain branching T- and/or Q-units. Can I impart especially good cleaning
How do silicone resin paints behave with They can also contain linear components properties to a matte interior paint by
respect to dirt pick-up? of D- and M-units. Depending on the adding silicone resins?
The claim that silicone-containing coat- amount of linear components, customized Producing a hydrophobic paint surface by
ings with a high water-beading effect are resins with high or low hardness can be adding silicone resin is not sufficient to
self-cleaning has not been shown in prac- formulated. impart good cleaning properties to a coat-
tice. On the contrary, silicones in coatings ing. Whether or not a coating can be
tend to promote soiling of the surface. As Should silicone resin hydrophobing addi- cleaned easily is determined by the overall
silicones are necessary to reduce the cap- tives be regarded as binders? formulation. A silicone hydrophobing
illary water uptake, it is necessary to find Silicone resin paints are formulated with additive can nevertheless contribute to
the best compromise amount. With the an organic binder dispersion and a sili- the cleanability of the coating.
most recent generation of silicone resins, cone resin. Often the amount of binder
between 4-7% produces a good balance dispersion is in the region of 8 to 20% Can I make deductions about the capil-
between dirt pick-up and capillary water and that of the silicone resin between 4 lary water uptake of a paint from the
uptake. and 10%. If the amount of silicone resin contact angle?
in the formulation is altered and coating The contact angle and the capillary water
What is the difference between a sili- properties such as water vapor transmis- uptake refer to two fundamentally differ-
cone resin and a silicone oil? sion or wet abrasion resistance compared ent things. The contact angle describes
In terms of chemical structure, silicone with a formulation in which the organic the wettability of a coating surface by
resins and silicone oils differ in the way binder has been altered by a similar water. High contact angles indicate poor
the molecules are branched. Silicone oils amount, it is noticeable that both formu- wettability and a concomitant water
(also known as polysiloxanes) have a lations do not change in the same way. beading effect. The capillary water uptake
linear structure composed of M- and Raising the amount of organic binder describes the capillary hydrophobicity of a
D-units. Silicone resins are branched and leads to a higher water vapor diffusion coating. It is quite possible for a coating to
contain T- and/or Q-units. Silicone resins resistance and a higher wet abrasion have high (and consequently unfavorable)
which contain only T- and Q- units have resistance; whereas these two properties capillary water uptake even though the
a very closely meshed resin network and remain virtually unchanged for changes in beading effect is very strong.
high hardness. If they also contain D- silicone resin. This indicates that the sili-
and/or M-units, the resin forms a more cone resin is not behaving as a binder. It is
open network with lower hardness. The therefore questionable if the silicone resin
real physical difference between a silicone should to be included as a binder when
oil and a silicone resin is the film forming calculating the PVC.
properties. Silicone oils do not form films;
that is to say that from an emulsion or
solution they dry to an oily layer. In con-
trast, silicone resins form a non-tacky soft
to hard silicone resin film.

Technical Background_Hydrophobing Agents page 123


Co-Binders
TEGO AddBond TEGO VariPlus
TEGO AddBond
Polyester resins as co-binders
Adhesion is a key topic in coatings sys- range of polyester resins which improve
tems. The demands made on adhesion- adhesion of solventborne, waterborne
promoting products are highly sophisti- and radiation-curing coatings and printing
cated. Besides excellent compatibility inks regardless of the way they dry or
with other formulation components, such cure. The resins can be used in physically
resins must be able to optimize adhesion drying, oxidatively drying, heat-curing
on all types of substrates. TEGO Add- and radiation-curing systems.
Bond products provide formulators with a

O O O O O O
(2n1) H2O
n HO R1 OH + n HO R2 OH HO R1 O R2 O H HO R1 O R2 O H
n COO NR
-
4
+ n
Figure 1: General reaction (schematic) for the manufacture of TEGO AddBond resins Figure 2: Structure of an aqueous dispersion of a
TEGO AddBond resin

How are polyester resins manufactu- boxyl groups with amines (fig. 2). Such
red? solvent-free dispersions have a good stor-
age life. The TEGO AddBond resins are
TEGO AddBond resins are polyester resistant to hydrolysis. They always con-
resins with a special structure. They are tain free carboxyl and hydroxyl groups.
manufactured by the polycondensation of Their hydrophilic and hydrophobic char-
special-purpose carboxylic acids and poly- acteristics are designed to make a maxi-
ols (fig. 1). Aqueous secondary disper- mum contribution to improving adhesion
sions are obtained by neutralizing car- and enhancing corrosion protection.

Technical Background_Co-Binders page 125


Some properties of TEGO AddBond products

Viscosity Softening Acid value Hydroxyl value


Product Supply form (23C, mPas) temperature (C) (mg KOH/g) (mg KOH/g)

TEGO AddBond LTH solid 600 15001 90 102 12 20 ~ 252

TEGO AddBond LTW 60 % in xylene 350 650 soft resin 20 30 ~ 302

TEGO AddBond LTW-B 60 % in n-butyl acetate 350 650 soft resin 20 30 ~ 302

TEGO AddBond 2220 ND 60 % in Solvesso 150 1500 2700 soft resin 18 22 ~ 302

TEGO AddBond 2325 60 % in n-butyl acetate 300 700 ~ 60 ~ 18 ~ 162

TEGO VariPlus 3350 UV 50 % in TPGDA ~ 8000 ~ 60 ~ 18 ~ 162

TEGO AddBond 1270 70 % in sec-butanol 4000 9000 soft resin 56 65 ~ 252

TEGO AddBond DS 1300 45 % in water ~ 150 ~ 55 ~ 602

TEGO AddBond HS 75 % in n-butyl acetate 1500 - 2500 soft resin 20 - 30 ~ 1002

1
60% in xylene 2
solid resin Table 1

What do polyester resins achieve? sion which does not contain any organic for use in multicoat finishes. In effect-
solvents. All other products are dissolved finishes, they improve cohesion within
With the exception of TEGO AddBond in an organic solvent. the film. The adhesion promoting proper-
LTH, which is a solid resin, all other prod- ties of TEGO AddBond products, com-
ucts in the TEGO AddBond range are TEGO AddBond resins contribute to plemented by excellent resistance to
supplied as solutions (table 1). Since improved adhesion on numerous sub- hydrolysis, significantly improve the anti-
TEGO VariPlus 3350 UV is also a poly- strates. They are effective on metals, min- corrosion performance of coatings.
ester resin, it is listed here. This resin is erals and various plastics and are thus TEGO AddBond resins help to enhance
dissolved in tripropyleneglycol diacrylate, often used in primers or one-coat fin- gloss, flexibility and hardness.
a UV-reactive solvent. TEGO AddBond ishes. They also improve intercoat adhe-
DS 1300 is an aqueous secondary disper- sion so they are highly recommended

Figure 3: Use of
TEGO AddBond LTW
in coil coatings

page 126 Technical Background_Co-Binders


Areas of application of TEGO AddBond resins

LTW/ VariPlus
HS LTH LTW-B 2220 ND 2325 1270 DS 1300 3350 UV

Can Coating + + + o

Coil Coating + + + o

Automotive OEM finishes + o + +

Container lacquers + o + o + o

Floor coatings +

Metal finishes + + + + + + +

Can coating lacquers + + + + o +

Finishes for plastics + + + + + + + + (UV)

Anti-corrosion paints + + + + + +

Primers (air-drying) + o +

Primers (baking systems) + o + + o o +

Printing inks + + (UV)

Road marking paints + + + + +

Waterborne coatings + +

Adhesives + + + o o + o (UV)

Hot embossing foils + +

UV coatings + +

+ recommended use o possible use limited use

TEGO AddBond resins are used as co- An additional important area of applica-
binders in numerous paints and lacquers tion is automotive OEM or refinish coat-
such as can coatings and coil coatings, ings. TEGO AddBond LTW and LTW-B
automotive OEM or refinish coatings, are widely used in solventborne finishes.
industrial coatings, anti-corrosion paints, TEGO AddBond 1270 is used in brake
road marking paints, printing inks, adhe- disc lacquers. TEGO AddBond DS 1300
sives, hot embossing foils and UV coat- is used, for example, to improve the adhe-
ings. sion of waterborne paints on plastic fend-
ers (fig. 4).
Figs. 3 to 7 show typical examples of
applications. TEGO AddBond LTW and TEGO AddBond products are also used
LTW-B improve adhesion of can coatings in anti-corrosion paints, TEGO AddBond
and coil coatings (fig. 3). These resins LTH and LTW in solventborne coatings,
exhibit a flexibilizing effect and enhance and TEGO AddBond DS 1300 in water-
the coatings processing properties. borne coatings (fig. 5).

Technical Background_Co-Binders page 127


Figure 4: Use of TEGO AddBond DS 1300 in automotive Figure 5: Use of TEGO AddBond LTH in anti-corrosion paints
finishes

TEGO AddBond products improve adhe- 1300 and 1270 for waterborne finishes acrylic resins and reactive thinners,
sion in numerous paints and lacquers for and TEGO AddBond LTH and TEGO TEGO VariPlus 3350 UV is recom-
plastics substrates such as polyamide, VariPlus 3350 UV for radiation-curing mended for use in radiation-curing coat-
polyvinylchloride, polycarbonate, ABS, coatings. The flexible TEGO AddBond ings, printing inks and adhesives (fig. 7).
ABS/polycarbonate, Noryl or HIPS. The LTW ensures good substrate wetting, TEGO AddBond LTH is also used in
TEGO AddBond products LTH, LTW, improved adhesion and excellent cohesion some UV formulations. Both resins
LTW-B, 2325 and 1270 are recom- of effect pigment finishes (fig. 6). enhance not only adhesion but also
mended for solventborne finishes, DS Because of its high compatibility with reduce volume shrinkage during curing.

Figure 6: Use of TEGO AddBond LTW in plastic coatings Figure 7: Use of TEGO VariPlus 3350 UV in UV printing inks

page 128 Technical Background_Co-Binders


TEGO VariPlus
Ketone-aldehyde resins and special resins derived from them

Numerous coatings and printing inks are good solubility in the solvents commonly stantially on the ketone used. If acetophe-
available commercially. Physically-drying used in these systems make them highly none or trimethylcyclohexanone are used,
coatings, air-drying paints, stoving enam- versatile. resins with exclusively keto groups are
els and radiation-curing systems are used obtained (fig. 1). It is possible to manu-
in diverse fields and applied to very dif- facture ketone resins containing hydroxyl
ferent substrates. TEGO VariPlus resins How are ketone-aldehyde resins and groups by using suitable reaction condi-
are frequently used to enhance the prop- the special resins derived from them tions and cyclohexanone.
erty profile of such systems. These non- manufactured?
saponifiable, neutral, hard resins have a
low molecular weight, low inherent color Ketone-aldehyde resins are manufactured
and exhibit good light and heat resistance. by an aldol condensation of a ketone with
Their outstanding compatibility with the an aldehyde. The resulting chemical struc-
most important main binders and their tures and their properties depend sub-

O O

n
HO
O
n n
Figure 1: Typical structures of
TEGO VariPlus resins based on TEGO VariPlus AP TEGO VariPlus TC TEGO VariPlus CA
ketone-aldehyde chemistry

Technical Background_Co-Binders page 129


O
n n n
R
OH O N N O

H H
Figure 2: Typical structures of
TEGO VariPlus SK TEGO VariPlus 1201 TF TEGO VariPlus resins based on
modified ketone-aldehyde resins

Another possibility for obtaining alcohol Another method ensures water-compati- hyde resins are also substantially improved.
groups is by hydrogenating the keto bility by incorporating polyether chains. The solubility of TEGO VariPlus resins in
group. In this way, the ketone-aldehyde This enables TEGO VariPlus UC to be organic solvents is very good. The polar-
resin TEGO VariPlus AP is made into the used to manufacture a water-soluble poly- ity determines the solubility in very polar
polyol resin TEGO VariPlus SK (fig. 2). etherketone resin which is also soluble in (alcohols) or very non-polar (aromatic-
The polyurethane-polyol resin TEGO organic solvents. free white spirit) solvents. With one
VariPlus 1201 TF is manufactured by exception, all TEGO VariPlus resins are
reacting the hydroxyl groups of TEGO hard solids. The glass transition tempera-
VariPlus SK with a special light-resistant How do ketone-aldehyde resins and ture ranges from -47C to +130C.
polyisocyanate using an organotin-free special resins derived from them per- While most resins are supplied as solids,
catalyst. form? TEGO VariPlus 1201 TF is supplied in an
organic solvent. As an aqueous secondary
Resins for waterborne applications can be As a result of their chemical structure and dispersion with excellent stability, TEGO
manufactured by various means. Water- the production process, the ketone-alde- VariPlus DS 50 is free from organic sol-
insoluble resins, for example, are ren- hyde resins are very light in color and vents. TEGO VariPlus UC is the only
dered water-dispersible by neutralization transparent compared with natural resins. solvent-free, liquid resin with a low glass
of the carboxyl groups. These polyure- The inherent color and resistance to light transition temperature of -47C.
thane-polyol dispersions are resistant to and heat of the special resins obtained by
hydrolysis (fig. 3). chemical modification of the ketone-alde-

n n
PIC PIC
O O O O
- +
COO NR 4

Figure 3: Structure of
TEGO VariPlus DS 50 the water-dispersible
TEGO VariPlus DS 50

page 130 Technical Background_Co-Binders


Physical properties of TEGO VariPlus resins

Color value Softening temp./ Tg OH-value


Product Supply form Gardner Melting temp. (C) (C) (mg KOH/g)

TEGO VariPlus AP solid 3 ~ 75 ~ 50 ~5

TEGO VariPlus TC solid 3 ~ 65 ~ 40 ~ 10

TEGO VariPlus CA solid 2 ~ 102 ~ 75 ~ 200

TEGO VariPlus SK solid 1 ~ 115 ~ 90 ~ 325

TEGO VariPlus 1201 TF 49% in EA 2 ~ 163 1


~ 130 1
~ 2001

TEGO VariPlus DS 50 33% in water ~ 1501 ~ 120 ~ 190

TEGO VariPlus UC liquid <7 ~ 47 ~ 40

TEGO VariPlus UC W 40 40% in water ~ 47 ~ 40

solid resin
1

As a result of the optimized process, the faster drying and set times better mechanical resistance
formaldehyde content of products based lower VOC content better corrosion protection
on acetophenone is below the limits of higher hardness better block resistance
detectability. higher gloss higher pigment loading and higher
improved adhesion color intensities through improved pig-
Because of their low molecular weights improves ability to be used in primers ment wetting
and high softening or melting tempera- better heat resistance lower pigment paste viscosities
tures, resins in the TEGO VariPlus range better chemical resistance
are not film-forming. They are thus com-
bined with other binders to improve the
properties of coatings.

TEGO VariPlus resins influence in all


sorts of ways the properties of solvent-
borne, waterborne and radiation-curing
coatings, printing and other inks as well
as of adhesives:

Figure 4: Use of
TEGO VariPlus 1201 TF
in printing inks

Technical Background_Co-Binders page 131


Areas of application of TEGO VariPlus resins
+ recommended use
UC/UC o possible use
AP SK 1201 TF CA TC DS 50 W 40 limited use

Wood finishes + + + o +

Coatings for plastics o + + + + +

Anti-corrosion coatings + + + o o

Concrete coatings + + o

Road marking paints + + + o

Industrial finishes + + + o + o

Paper coatings + + + +

Writing inks + o +

Adhesives + o + + o

Pigment pastes o o + o + + +

Printing inks + + + +

Hot embossing foils + + +

UV coatings + + o o o o

Besides their widespread use in printing marking paints, industrial finishes, pack- gloss, and good block resistance during
inks (rotogravure, flexographic, screen aging coatings, paper coatings, writing rapid drying. Because of its very good
printing, uv and specialist printing pro- inks, pigment pastes, liquid adhesives and pigment wetting, it is also used in pig-
cesses) and hot embossing foils, TEGO hot melt adhesives. ment pastes to achieve high color inten-
VariPlus resins are proven co-binders in sity and good transparency.
coatings and adhesives. They are used in Figures 4 to 7 show typical applications.
wood finishes, coatings for plastics, anti- TEGO VariPlus 1201 TF imparts printing
corrosion paints, concrete paints, road inks with very good adhesion, excellent

Ballpoint pen pastes owe their special


rheological properties to the unique
structure of TEGO VariPlus SK. This
resin prevents drying out and leakage of
the ink while ensuring rapid setting after
writing.

Figure 5: Use of TEGO VariPlus SK in ballpoint pen pastes

page 132 Technical Background_Co-Binders


Figure 6: Use of TEGO VariPlus DS 50 in coatings for plastics

Used as a resin in the top coat of hot plastics to water, solvents and chemicals oped specifically for solventborne,
embossing foils, TEGO VariPlus CA has as well as their film hardness and gloss. extremely high-solids pigment concen-
a positive influence on a range of proper- Substrate adhesion is also optimized. trates with high pigment loadings. TEGO
ties such as gloss, flexibility and fastness. VariPlus UC W 40 makes this resin acces-
It is also used in the adhesive film of these TEGO VariPlus TC has proved itself as a sible for use in waterborne (including uni-
coated foils because it enhances adhesion. grind paste resin in pigment concentrates versal) pigment preparations.
because of its universal solubility in
Because of its high glass transition tem- organic solvents, compatibility with bind-
perature and special chemical structure, ers and excellent pigment wetting.
TEGO VariPlus DS 50 improves the TEGO VariPlus UC represents a new
resistance of waterborne coatings for generation of pigment paste resins devel-

Figure 7: Use of TEGO


VariPlus TC in pigment
pastes for coatings

Technical Background_Co-Binders page 133


Silicone Resins
SILIKOPHEN SILIKOFTAL SILIKOPON
Silicone resins and silicone combination resins

An important reason for the wide applica- These properties make silicone resins and
tion and commercial success of silicone silicone combination resins widely appli-
resins are properties such as: cable in areas such as impregnation of
thermal stability concrete, high-temperature resistant coat-
weathering resistance ings or weather resistant exterior coat-
maintaining elasticity at low tempera- ings. These binders are used in the form
tures of solutions, liquid resins and emulsions.
low surface tension
hydrophobicity, surface activity
release and lubricating properties

General introduction and manufacture (Si-O-Si), also found in silicates, is


ca. 280C of silicone resins responsible for the inorganic character.
catalyst
Si+R-CI RxSiCI4-x The organic properties arise from the
Silicones are organic silicon compounds direct link between silicon and carbon.
Figure 1: Mller-Rochow synthesis
known as polyorganosiloxanes. This prod-
uct group can be defined simply as fol- The starting point for manufacturing sili-
lows: cone resins are the chlorosilanes which
they are polymers are obtained on a large scale by the Ml-
silicon is directly bonded to carbon ler-Rochow synthesis. In this, very pure
there is at least one oxygen atom con- silicon (>98%) is reacted at 280C in the
nected to the silicon presence of catalysts and promoters with
chemicals such as methyl chloride or phe-
The silicones occupy a hybrid position nyl chloride in a fluidized bed reactor
between inorganic and organic com- (fig. 1).
pounds, specifically between silicates and
organic polymers. The siloxane link

Technical Background_Silicone Resins page 135


Structural units for forming polymeric siloxanes (R: methyl or phenyl groups)

Basis monomer Functionality in terms of hydrolyzable groups Structural unit in the polymer Symbol

SiX4 tetrafunctional (form spatial structures) SiO4/2 Q

R-SiX3 trifunctional (form spatial structures) RSiO3/2 T

R2-SiX2 difunctional (form chains) R2SiO2/2 D

R3-SiX monofunctional (chain breaking or terminating) R3SiO1/2 M

Table 1

The composition and number of the struc- etwork of three-dimensional and cyclic
n Varying the resin intermediates and poly-
tural units and the functional groups on structures is formed. Because of this com- ols enables the following series of prod-
the silicon atom determine the structure, plexity, precise chemical structural formu- ucts to be manufactured:
processing, and complex properties of the las cannot be given. In general, silicones "pure" phenyl methyl silicone resins
silicone resins. Table 1 shows the struc- are described in terms of their different (SILIKOPHEN) with silicone content
tural elements for forming polyorganosi- substituents and reactive groups (fig. 3). of approximately 95%, both solvent-
loxanes. based and as aqueous emulsions
Various techniques have been developed silicone polyester (SILIKOFTAL) with
for further modification of the resin inter- silicone content of 30 to 80%
Silicone resin manufacture by Evonik mediates. All Evonik silicone resins are silicone-epoxide hybrid binders
manufactured using a common reaction (SILIKOPON) with silicone content of
Chlorosilanes, the starting materials for scheme. First, resin intermediates with 50%
silicone resins, are generally reacted with well-defined molecular weight and con- silicone-modified, aqueous polyure-
water or alcohols (methanol or ethanol) taining almost exclusively SiOR- rather thane dispersions (SILIKOPUR)
to produce resin intermediates with than SiOH-reactive groups are produced.
molecular weights (MW) between 1,000 These are crosslinked further with polyols Because they also contain only a small
and 3,000 g/mol. These have many OH- to produce single phase products with a amount of an organic component,
and/or OR- end-groups and no longer long shelf life. SILIKOPHEN resins exhibit excellent
contain chlorine. During hydrolysis/alco- heat resistance. Figure 4 describes
holysis of the silane mixture, a dense SILIKOPHEN and SILIKOFTAL resin
manufacture at Evonik.

Crosslinking of SILIKOPHEN and SILIKOFTAL


silicone resins

Chemical Reactions Equations (1) and (2) describe the reac- manufacture and also during curing.
tion of chlorosilanes with water and alco- Reactions (4) to (6) are particularly
In general, only a few chemical reactions hol. They occur only during the manufac- important during manufacture as they
are important in the manufacture and cur- ture of the resin intermediate. Reactions lead to an increase in molecular weight.
ing of silicone resins (fig. 2). (3) to (6) take place both during resin

page 136 Technical Background_Silicone Resins


(1) SiCl + H2O > SiOH + HCL 
(2) SiCl + ROH > SiOR + HCL   
(3) SiOR + H2O > SiOH + ROH  
(4) SiOH + SiOH > SiOSi + H2O   
   
(5) SiOH + SiOR > Si-O-Si + ROH      
(6) SiOR + ROH > SiOR + ROH    

     
R = polyol residue R = CH3, C2H5      
Figure 2: Chemical reactions        
   
  


    

 

  
 
 
 
The silicone intermediates and organic 
 
components such as polyols are not com-
Figure 3: Structure of a silicone resin (idealized, R: methyl or phenyl groups)
patible with each other at the beginning
of the modification process. They only
become compatible and homogenizable
as a result of the chemical reactions. The
reaction is stopped when the desired
molecular weight is reached. Product group SILIKOPHEN
Polyol
Phenyl-
The partially completed modifying reac- methyl silicone
resin
tion (6) is resumed during curing. This
involves further reaction of the remaining
Methyl/Phenyl
functional groups in a system which is
Silane Resin Intermediate Resins
already strongly crosslinked and for
SILIKOPHEN and SILIKOFTAL can only
occur at high temperatures. Stoving tem- Product group SILIKOFTAL

peratures of at least 200C are necessary Polyester


to ensure complete curing. Silicone-
polyester

Methyl/Phenyl
Crosslinking of silicone resins in the
Silane Resin Intermediate Resins
coating
Figure 4: Resin manufacture at Evonik

In general, various catalysts only have a


limited effect on accelerating the curing
reactions of SILIKOPHEN and
SILIKOFTAL resins. The use of large
   
amounts of catalyst to reduce burn-off
temperatures is restricted as problems           
such as low storage stability, gelling or     
increased tendency to yellowing can
occur. For complete curing without addi- Figure 5: Crosslinking reaction of silicone resins
tion of catalyst, we recommend stoving
for 30 minutes at an object temperature
of 250C (figure 5 shows the crosslinking
reaction of the silicone resins).

Technical Background_Silicone Resins page 137


Applications of silicone resins and Phenylmethyl silicone resins
SILIKOPHEN P resins
silicone combination resins
Evonik offers a range of phenyl methyl
silicone resins under the trade name
SILIKOPHEN. The high phenyl group
Guiding formulation for a coating based on SILIKOPHEN P 80/X content ensures excellent heat resistance
with temperature resistance to 500C as well as good compatibility with other
organic resins. As with all phenylmethyl
Component Amount by weight Ingredient
silicone resin coatings, those based on
SILIKOPHEN P80/X 42.5 Silicone resin
SILIKOPHEN P resins are thermoplastic.
TEGO Dispers 670 1.0 Dispersing additive

Bentone 38 0.3 Rheological additive Illustration 1 gives an overview of the


temperature stability achievable. This
Isobutanol 0.5 Alcohol
depends strongly on the formulation,
Butylglycol acetate 1.2 Glycol ester
particularly on the pigmentation. While
TEGO Airex 900 0.5 Deaerator silicone resins with ethyl or propyl groups
Heucodur 9-100 6.0 Black pigment have low temperature stability, the heat
resistance is distinctly raised if phenyl or
Heucophos ZPO 6.0 Corrosion protection pigment
methyl groups are incorporated resulting
Mica TM 17.0 Mica
in resins with extraordinary heat resis-
Aerosil 200 0.5 Pyrogenic silica tance up to 350C.
Xylene 24.5 Solvent
Such coatings are used mainly in corro-
Total 100.0
sion protection at high temperatures such
Table 2 as car exhausts, smoke stacks, industrial
kilns and combustion chambers (fig. 6).
The property profile of coatings based
on SILIKOPHEN P resins is strongly
Maximum service temperatures of binders
dependent on the formulation. For heat
Temperature Silicone- Methyl- Phenylmethyl- resistance up to 350C, formulations
in C Polyester polyester silicone silicone with heat resistant inorganic colored
700 pigments and titanium dioxide are used.
The guiding formulations in tables 2 and
600
3 give examples for long-term tempera-
500 ture levels of 500 and 600C.
400

300

200

100

Illustration 1 heat resistance as a function of pigmentation continuous heat resistance

page 138 Technical Background_Silicone Resins


SILIKOPHEN P resins are characterized
by very good pigment wetting. The
films remain fully functional even after
extended exposure to temperatures of
350C but may gradually lose their gloss.
The maximum thickness of such coatings
should (depending on their pigmentation)
be less than 25 (5) m, otherwise sol-
vent blistering can be caused by alcohol
liberated on stoving.
Figure 6: Application of SILIKOPHEN resins

In addition to this, too high a cured coat-


ing thickness looses flexibility when
exposed to long-term temperatures over
300C. Flexibility of such high tempera-
ture coatings is obtained by using lamellar Coatings resistant to temperatures in High solid silicone resin SILIKOPHEN P
fillers such as mica or aluminum flakes. excess of 700C can be manufactured 80/X or silicone resin emulsion SILIKO-
Care must still be taken to ensure the using ceramic powders. However, the PHEN P 40/W can satisfy demands for a
same dry coating thickness as above. entire coated surface must be heated reduction in solvent emission. Table 4
above the melting point of the frit. Only gives a guiding formulation for a water-
Primers formulated with zinc dust can be then are permanently bonded, enamel- borne application based on the silicone
used for corrosion-resistant coatings up to like coatings produced by sintering with resin SILIKOPHEN P 40/W which can
450C. Coatings which maintain their the siloxane backbone. withstand continuous use at temperatures
protective effect up to 600C are formu- up to 500C.
lated using flake inorganic or metallic pig-
ments such as aluminum and mica (table 3).

At temperatures above 350C, the


organic components of the resin are Guiding formulation for a coating based on SILIKOPHEN P 80/X
almost completely burned off. Aided by with temperature resistance to 600C
sintering, inorganic composites are
Component Amount by weight Ingredient
formed which are very hard and com-
pletely chemically inert but at the same SILIKOPHEN P80/X 52.0 Silicone resin

time very brittle. Burning off organic TEGO Airex 900 0.5 Deaerator
groups, especially the phenyl substituents Blanc fixe N 15.0 Filler
of SILlKOPHEN P resins, leaves micro-
Aerosil 200 0.5 Pyrogenic silica
scopically small voids. The resulting
matrix system is so flexible that coatings Stapa 4 20.0 Aluminum

at a temperature of 600C can be Xylene 12.0 Solvent


quenched repeatedly with cold water Total 100.0
without cracking.
Table 3

Technical Background_Silicone Resins page 139


Guiding formulation for a high-temperature resistant coating based on
SILIKOPHEN P 40/W with temperature resistance to 500C

Component Amount by weight Ingredient

Water 26.1

TEGO Dispers 750 W 1.5 Dispersing additive


Metals such as tin can leach out of metal TEGO Foamex K 3 0.2 Defoamer
cans and lead to formation of gel parti-
Ammonium hydroxide 25% 0.2 Base
cles. Therefore, manufactured paints
should not be stored or packaged in this Heucodur Schwarz 9-100 8.0 Black pigment

type of container. Heucosil CTF 5.0 Corrosion protection pigment

Mica TM 14.0 Mica

SILIKOPHEN P40/W 45.0 Silicone resin


Silicone-polyester resins/
SILIKOFTAL HT grades Total 100.0

Table 4
Silicone-polyester resins combine the
good properties of silicone resins (tem-
perature resistance, weathering resistance
and low surface tension) with those of
polyesters (low thermoplasticity, high
flexibility and good pigment wetting). greater than 50%, the silicone component ent properties. Evonik offers a wide range
stabilizes the organic component so that of SILIKOFTAL HT silicone-polyester
By using thermally-stable polyesters, no noticeable yellowing occurs. The prob- grades which are customized for specific
binders can be produced with a continu- able reason for this is that the higher sili- requirements.
ous high temperature resistance of cone content increases the inorganic con-
250C. tent in the whole polymer thereby The polyester content ensures good
decreasing thermal oxidation. pigment wetting. Thus, for example,
With silicone content below 50%, expo- white coatings can be produced with
sure to a temperature of 300C for three By varying the polyesters and silicone gloss values greater than 90 (20 angle).
hours produces strong yellowing, typical resin intermediates, it is possible to pro- Because of the resistance to yellowing,
of an organic resin. With silicone content duce silicone-polyester resins with differ- very light colors can also be formulated.

page 140 Technical Background_Silicone Resins


Figure 7: Toaster Figure 8: Frying pan bottom

A further characteristic of coatings based The properties of SILIKOFTAL HT washer without damage using surfactant-
on SILIKOFTAL is their low thermoplas- grades are particularly advantageous in containing, strongly-aIkaline cleaning
ticity. As both the silicone and polyester decorative coatings of thermally stressed agents. Resistance of a coating to deter-
portions are strongly crosslinked, the appliances such as toasters, tanning beds, gents is generally determined by the for-
hardness is maintained even at tempera- fan heaters and cookers as well as the mulation, particularly the binder used. It is
tures around 150C. outer coatings of deep fryers, pots and an important criteria for the quality of sili-
pans (figs. 7 and 8). cone polyesters.
This is important in applications in which
the hot coatings are mechanically stressed Coatings of some household items must The most important properties of differ-
but must be scratch-resistant. be resistant to detergents so that they can ent SILIKOFTAL HT grades are shown in
withstand frequent cleaning in a dish- table 5.

SILIKOFTAL grades

Product Silicone
Siliconecontent
content Properties
Properties

retains hardness
retains from
hardness room
from roomtemperature
temperature to 150C; long-term
to 150C; long-termheat resistance
heat to 250C;
resistance to 250C;
Silikoftal HTT 80% goodgood detergent
detergentresistance. Currently
resistance. listed FDA
Listed under under175.300
FDA 175.300 insolvent-free
in cured cured solvent-free
resins. resins;
Silikoftal HTT 80% conforms to BfR.*
very good resistance to yellowing up to 220C. Listed under FDA 175.300 in cured
Silikoftal HTS 70% very good resistance
solvent-free resins.to yellowing up to 220C. Currently listed under FDA 175.300 in
Silikoftal HTS 70% cured solvent-free resins; conforms to BfR.*
flexible and therefore to a limited extent may be deep drawn. Listed under
Silikoftal HTF 50% flexible and therefore
FDA 175.300 to a solvent-free
in cured limited extent may be
resins; deep drawn.
conforms to BfR.Currently listed under
Silikoftal HTF 50% FDA 175.300 in cured solvent-free resins; conforms to BfR.*
high gloss and low thermoplasticity. Listed under
Silikoftal HTL 50% high FDAgloss and low
175.300 inthermoplasticity.
cured solvent-free Currently
resins. listed under FDA 175.300 in cured solvent-free
Silikoftal HTL 50% resins; conforms to BfR.*
high gloss, low thermoplasticity, good detergent resistance. Listed under FDA 175.300
Silikoftal HTL 2 50% high in gloss,
cured low thermoplasticity,
solvent-free resins. good detergent resistance. Currently listed under
Silikoftal HTL 2 50% FDA 175.300 in cured solvent-free resins; conforms to BfR.*
very good yellowing resistance up to 200C, very good boiling water resistance.
Silikoftal HTL 3 30% very goodunder
Listed yellowing resistanceinupcured
FDA 175.300 to 200C, very good
solvent-free boiling
resins; waterto
conforms resistance.
BfR. Currently
Silikoftal HTL 3 30% listed under FDA 175.300 in cured solvent-free resins; conforms to BfR.*

Table 5
*Please note that the evaluation regarding suitability for food contact may change, you can find the latest status on our website www.tego.de

Table 5

Technical Background_Silicone Resins page 141


Suitable solvents for silicone-polyester OH content Silicone epoxide combination resins/
resins SILIKOPON E grades
The free OH-content of SILIKOFTAL
In unbaked form, silicone-polyesters still resins is not specified. When manufactur- The SILIKOPON range combines the
have a high OH-content. These polar ing these products, the emphasis is on properties of the widely applicable epox-
groups interact strongly with the ester clarity and viscosity rather than constant ide resins with those of silicone resins.
groups. In the manufacture of the resin, OH-value. SILIKOPON EW and SILIKOPON EC
polar solvents are therefore used to are for high-temperature use. Compared
inhibit association and thus maintain a with pure silicone resins (SILIKOPHEN),
stable viscosity. If interactions occur, such Stoving conditions and catalysts these silicone/epoxy hybrids offer better
as during cooling, these associations only adhesion to metals as well as better corro-
break up slowly upon warming. In general, the curing reactions of sion protection and chemical resistance.
SILIKOFTAL resins are accelerated by A typical application is in vehicle exhaust
There is a time delay in physical proper- various catalysts. The use of large amounts coatings where SILIKOPON EW or
ties such as viscosity and conductivity of catalyst to significantly reduce stoving SILIKOPON EC is used in primers and a
reaching their final value. When formu- temperatures is not recommended as it SILIKOPHEN resin in top coats. Such
lating coatings, polar solvents such as can lead to problems such as poor storage two-coat systems are temperature resis-
ketones and esters are preferred to avoid stability, gelling, brittleness and increased tant to 550C and have excellent corro-
clouding. The use of aliphatic solvents is tendency to yellowing. sion resistance.
not recommended.
To achieve full curing without addition of Alongside silicone/epoxy hybrid resins
catalysts, the following conditions are rec- for use at high temperatures, SILIKO-
ommended: PON EF is a further hybrid for use in
60 minutes at 220C topcoats in general industrial and mari-
30 minutes at 250C time applications.
15 minutes at 280C

page 142 Technical Background_Silicone Resins


Dynasylan
SILIKOPON (3-aminopropyl)-triethoxy-silane

Aliphatic Epoxy
H2O H2N
SILIKOPON EF is used as a binder for O
ultra high solids applications in corrosion
CH CH3
protection coatings for steel, coatings for R4
wood and concrete and maritime applica-
tions such as biocide-free, easy-to-clean
Alkoxy Silicone resin
coatings particularly above the water line. -ROH RO Si OR
R1

The special feature of the chemical cross- R2 Si OR4 OR


linking of SILIKOPON EF lies in the dual-
R3 R = Me or Et
cure mechanism at room temperature: the
nucleophilic opening of the epoxide ring
Figure 9: The Dual-Cure Mechanism
(by the amine) and the hydrolysis/con-
densation reaction of the alkoxy groups.
Both reactions occur in situ. The curing
agents are aminosilanes whose amine
groups react with the epoxide groups. The hydrolysis/condensation reaction isocyanate-free, 2-pack formulations with
The three alkoxy groups react in the pres- described in figure 9 can be strongly VOC content less than 250 g/l. In the
ence of water or moisture with the free accelerated by catalysts. These can be tin case of, for example, wood clear coats,
alkoxy group of the silicone resin by compounds or Lewis acids and illustration the VOC can be less than 100 g/l.
hydrolysis/condensation. This double 2 shows the reduction in drying time The silicone/epoxy resin combination
crosslinking allows the positive proper- achieved by a tin compound (DOTL) and allows two-coat corrosion protection
ties of organic and inorganic polymers to a Lewis acid (borontrifluoride/ethylamine coatings to be manufactured with SILIKO-
be combined in a new class of binders. complex). PON EF which can replace the classic
Because of the high crosslink density (see three-coat systems (fig. 10).
fig. 9), these coatings have a high dirt- This binder is suitable for ultra high sol-
repelling effect and are thus very effec- ids, eco-friendly coatings. The particular
tive against graffiti. advantage is that it permits production of

Effect of catalysts on the drying of SILIKOPON EF

Drying time/hours 0 1 2 3 4 5 6 7 9

SILIKOPON EF

EF + tin catalyst

EF + Lewis acid

Illustration 2 Touch drying Complete drying

Technical Background_Silicone Resins page 143


HO OH + HO OH + OCN NCO

1. Polyaddition COOH

PU

OCN NCO
COOH
175m
2. Neutralization + NHR3
Curing Agent
SILIKOPON

Epoxy

100m OCN NCO


- +
COO NHR3
1)
H2O
2)
polyamine
Primer Primer
3. Emulsification - +
COO NHR3
and crosslinking

Steel Steel + +
COO NHR3 COO NHR3
n

Figure 10: Coating structure Figure 11: Synthesis of polyurethane dispersions (schematic)

In addition to the reduced coat thickness The special properties are as follows: In contrast to this commonly-used synthe-
and hence less material needed, cost sav- quick drying in air sis, Evonik largely replaces the polyester-
ings also accrue because of the reduced non-stick effect polyol with a silicone base unit, a dihy-
time required for coating. Further advan- special haptics droxyalkylpolydimethyl siloxane with two
tages arising from the high inorganic con- hydrophobic terminal OH groups (fig. 12).
tent are good char resistance and high high flexibility even at low tempera-
abrasion resistance. The high crosslinking tures (-30C)
CH3
density of coatings based on SILIKOPON high elasticity of 300-400%
EF allows this binder to be used in the good adhesion to flexible substrates HO Si O OH
flooring and industrial plant sectors. improved abrasion resistance
CH3
n
Figure 12: Dihydroxyalkylpolydimethyl siloxane
Waterborne silicone-modified polyure- Manufacture of SILIKOPUR 8080
thane dispersions
The synthesis of polyurethane dispersions Applications of SILIKOPUR 8080
Under the name SILIKOPUR 8080, usually occurs as the series of consecutive
Evonik offers a waterborne, N-methylpyr- steps shown in figure 12. A diol, dimethy- An application of SILIKOPUR 8080 is
rolidone-free (NMP-free), silicone-modi- lolpropionic acid and excess isocyanate the coating of leather in, for example,
fied, 1-pack polyurethane dispersion. This are reacted together to form an isocya- shoes, clothing or vehicles. The polyure-
dispersion air-dries at room temperature. nate-terminated prepolymer. After neu- thane formulation increases the slip effect
tralization and chain extension, it is emul- and decreases creaking and squeaking of
sified in water. leather over the long-term.

page 144 Technical Background_Silicone Resins


non-silicone-modified polyurethane dispersion SILIKOPUR 8080

Test 1 to 1

sample number
1
load (N)

load (N)
path traversed (mm) path traversed (mm)

Figure 13: Slip properties

Figure 13 compares the slip properties Solid and non-volatile components


with those of a usual waterborne polyure-
thane dispersion.
As with all condensed binders, the amount of solids in
Because of the silicone modification and SILIKOPHEN, SILIKOPON and SILIKOFTAL is not exactly
the anti-stick properties and high flexibil- the same as the amount of non-volatiles. Solids contain low
ity resulting from it, SILIKOPUR 8080 is molecular resin components and condensed groups which
used in release coatings for EPDM. Fur- are not present in the non-volatile residue after drying.
thermore, the dispersion has good sub-
strate adhesion properties on many other Therefore, the solids content is often a few percent higher
plastics (ABS, GFP, Nornyl, PA, PMMA, than the non-volatiles as determined by DIN 53216. In our
PVC, PC). data sheets, only the amount of non-volatiles is given as this
is the parameter which is important for the user. In contrast,
Illustration 3 shows that a 30% addition the material safety data sheets give the solids content which
of SILIKOPUR 8080 as co-binder to an is what is important for hazardous goods classification.
acrylic dispersion can improve abrasion
resistance of wood finishes.

Abrasion resistance (CS-17 wheel, 1 kg)

Abrasion (mg) 10 20 30 40

200

150

100

50

Amount of SILIKOPUR 8080 (%)

Illustration 3 500 abrasion cycles 1,000 abrasion cycles

Technical Background_Silicone Resins page 145


Silica-Nanocomposites
NANOCRYL NANOPOX NANOPOL
Because of their special properties, nano- They:
composites are mainly used in coatings improve scratch and abrasion resistance
whose characteristics cannot be produced improve barrier properties
by conventional means or can only be improve total transparency of the
achieved by multiple coats. Silica-nano- coating
composites are preferred where high have no effect on the degree of gloss
scratch and abrasion resistance is needed reduce shrinkage during curing
at the same time as transparency. reduce tension stress during curing
improve adhesion on substrates with
Silicon dioxide nanoparticles can be used hydroxyl functions
in the form of liquid composites in many
organic matrices in coating materials. It follows from the above properties that
silica nanoparticles are favored in applica-
tions which require transparency and/or
high abrasion resistance such as high per-
formance coatings or off-shore topcoats.

Manufacture of silica-nanocomposites Starting from water glass (aqueous


sodium silicate solution), spherical silica
Composites can be manufactured from nanoparticles of ca. 20 nm diameter can
silica nanoparticles and organic resins be cultured in an aqueous environment
using a modified sol-gel process. Despite and their growth stopped by wet-chemi-
being 50% w/w filled, they are crystal cal means. These particles then have their
clear. surfaces modified to permit stable trans-
fer into an organic matrix.

Technical Background_Silica-Nanocomposites page 147


Depending on the matrix which will sur- dency to form agglomerates of m size Use of silica-nanocomposites to
round it, this modification is performed which cannot be re-dispersed. This would improve properties
with various agents and can lead to differ- lead to the loss of all the desirable proper-
ent results according to the polarity of the ties of the silica-nanocomposites, such as In addition to the main property of scratch
matrix and silica-nanoparticles. transparency and scratch and abrasion and abrasion resistance while maintaining
resistance. transparency, secondary properties such
In the first purification step, practically all as barrier effects or reduced shrinkage
free ions are removed. In a second step, In principle, a large range of different par- during curing can also be found in impor-
after surface modification with a process- ticle sizes can be produced. An average tant applications.
ing matrix, water is separated. In the third particle diameter of ca. 20 nm has how-
step, the processing matrix is replaced by ever proved optimum for: The particles in the cured film are statisti-
the final matrix. optical clarity in coating materials cally distributed. The distribution is, on
core/shell ratio average, identical at the surface, in the
Silica-nanoparticles obtained in this way, high amount of silica nanoparticles in middle and at the bottom.
contain, depending on the matrix, up to the liquid composite
50% silica in nanoparticulate form and storage stability
are stable for at least six months. These
products are crystal clear, completely Particle size distribution is very narrow as
transparent and show no sedimentation. a result of process optimization.
Particle size distribution

Free silica-nanoparticles cannot be pre-


pared by this process as, in the absence of
a surrounding matrix, they have a ten-

Silica phase
Route to silica-nanocomposites

Aqueous
Silicate Solution Agglomeration,
gelation, flocculation
particle density

H
Si O
Si
H O

Silica Sol
Surface SNC
modification Low viscosity,
waterclear, 0 20 40 60 80 100
no sedimentation
Matrix exchange particle size [nm]

The silica phase consists of discrete nanospheres ( 20 nm) with an


extremely narrow particle size distribution

page 148 Technical Background_Silica-Nanocomposites


Silica-nanocomposites provides steel wool resistance

TEM photo of nanoparticles Microscopic images of cured PPTTA (left) and Nanocryl C 165 (50% SiO2, right) after steel wool scratching

This is quite different from surface active additive. Both coatings were subjected to Addition of inorganic nanoparticles can
products such as waxes or silicone oils rubbing with commercial steel wool and alleviate shrinkage during curing. This is
which are only effective at the paint/air then viewed microscopically. The left important for coating substrates which
interface. Therefore, they only have a sample, which contains no nanoparticles, should not undergo any dimensional
temporary effect on the scratch and abra- has sustained heavy damage. In contrast, change during crosslinking (e.g., warping
sion resistance and provide protection the sample on the right containing silica- or distortion of panels, foil or filigrain
only over a few load cycles. Current rec- nanoparticles remains undamaged. components).
ommendations are for added amounts in
the region of 0.5%, as higher quantities
can lead to surface defects and incompati-
bilities.
Relationship pbw nanosilica/pencil hardness
In contrast, silica-nanocomposites offer
permanent protection because they are 6
firmly bound into the cured film matrix.
Pencil Hardness in H-Units

5
Because they are distributed throughout
the whole film, the initial recommenda- 4
tion is 5 to 10% w/w relative to the sol-
3
ids of the paint formulation. This amount
greatly improves hardness, scratch and 2
abrasion resistance in many applications.
1

The resistance to abrasion with steel wool 0


is shown for two PPTTA-based coatings 0 5 10 15 20
the coating on the right contains 50% pbw nanosilica particles
nanoparticles and that on the left has no

Technical Background_Silica-Nanocomposites page 149


The correct choice of low-shrinkage bind- incorporation of 50% w/w nanosilica and abrasion resistance and chemical
ers on the one hand and addition of nano- leads to a viscosity only four times higher resistance of print in the cosmetics sector
silica on the other is crucial for successful than with the original resin. or on bottles for high quality spirits have
formulation of clear coats. During curing, grown enormously, so that the use of
the nanoparticles achieve an even distri- The reason for this low increase in vis- silica-nanoparticles can be advantageous.
bution of forces. Furthermore, introduc- cosity lies in the monodispersed silica-
tion of inorganic components in amounts nanoparticles which, with their special Silica-nanoparticles are also suitable for
related to that of the shrinkable organic surface modification, show different applications where a barrier effect is
resins leads to smaller effects at the same behavior to, e.g., milled silicon dioxide required especially where transparency
film thickness. or fumed silica. The latter gives rise to an is also essential. The barrier effect in an
almost exponential increase in viscosity organic transparent coating is increased
Similarly, the so-called bending or curling at higher amounts which, at these levels, by the inorganic silica particles. Diffusion
effect which can occur with foils or end- would lead to a solid mass. of oxygen and water vapor is thus signifi-
less products is significantly reduced by cantly lower than in an unmodified
silica-nanoparticles. On substrates, such as glass and aluminum, clearcoat.
the glassy nanoparticles facilitate adhe-
As a result of the special surface modifica- sion since similar substances adhere well The addition of silica-nanoparticles also
tion of the nanosilica particles, the silica- to each other. This effect is exploited in, generates a barrier effect in the cured film
nanocomposites only produce a relatively for example, printing on high quality glass against solvents and can increase resis-
small increase in viscosity. In general, bottles. The demands made on scratch tance by up to 400%.

Relationship pbw nanosilica/loss of weight Relationship pbw nanosilica/haze

35 70

30 60
loss of weight in mg

25 50
delta haze

20 40

15 30

10 20

5 10

0 0
0 5 10 15 20 0 5 10 15 20

pbw nanosilica particles pbw nanosilica particles

page 150 Technical Background_Silica-Nanocomposites


In filler formulations containing In the cured, filled coating, the nanopar- The slight increase in viscosity caused by
microscale fillers or pigments, the ticles can position themselves in the gaps the nanoparticles also plays a part. The
nanoparticles can reduce settling of the between the filler and the pigment per- reduction of emissions by adding the par-
fillers. This can be attributed to the loos- mitting, on the one hand, a marked ticles as an extender in formulations is
ening effect of the nanoparticles which increase in the absolute filler content (of also worth mentioning.
position themselves between the mic- particular interest for high solids coat-
roparticles and prevent close particle ings) and, on the other, denser packing
packing. of all inorganic components.

Viscosity build-up of different SiO2 particles in PPTTA

25000

surface modified
Viscosity [mPas]

20000 fumed silica

15000

10000
monodisperse
5000 nanosilica

0
0 10 20 30 40 50
SiO2 content [wt%]

Technical Background_Silica-Nanocomposites page 151


Solvent migration via ERA (evaporation rate analysis)

TEMPEOTA

TEMPEOTA
PEA + SiO2
EPA + SiO2
AMPA

AMPA
+ SiO2

+ SiO2

+ SiO2
GPTA

GPTA
PEA
EPA
M-Value

1000

800

600

400

The degree of gloss of the formulation is film. Increased hardness, scratch and
not affected by the silica-nanoparticles. abrasion resistance can thus be achieved
Unlike surface waxes or pyrogenic silicas, in coatings of all degrees of gloss.
which are added as matting agents, the
nanoparticles do not settle out on the sur-
face but are, as already described, distrib- Use of silica-nanocomposites
uted statistically throughout the entire
Incorporation of the liquid composites is
easy. Like standard binders, the products
are thoroughly stirred together with the
main binder at the start of the production
process. Dispersing or bead milling is
unnecessary. Non-polar resins, solvents
or additives are especially unsuitable as
they cause the silica-nanoparticles to
agglomerate or precipitate.

In general, aromatic polyisocyanates


(TDI-based) are unsuitable as they rapidly
lead to agglomeration, even when used in
small amounts or in blends with aliphatic
or cycloaliphatic polyisocyanates. Suitable
alternatives are aliphatic and cycloaliphatic
polyisocyanates such as VESTANAT
T1890.

page 152 Technical Background_Silica-Nanocomposites


Permeabilities of N2 and O2 (DIN 53380) Water vapor permeability (DIN EN ISO 7783-2)

70 400
gas permeation [ml/m2hbar]

60 350

50 300

WVP [g/(m2d)]
40 250

30 200

20 150

10 100

0 50
0% 28% 50%
0
nano silica content 0% SiO2 20% SiO2 30% SiO2 50% SiO2

Nitrogen Oxygen
PPTTA-Film (20 m) on PET-Foil (75 m) PPTTA-Film (45 m) on cardboard

Amino-functional resins, such as amine Since the times at which such events These lists give reliable recommendations
synergists for radical-curing UV coatings manifest themselves may be very differ- for the compatibility of additives with the
or aminoplastics for 1-pack stoving enam- ent, storage tests at raised temperature, silica-nanocomposites in terms of short-
els, are mostly unsuitable. Compatibility e.g. 50C are recommended: and long-term shelf-life.
should, of course, always be checked in
the laboratory. to simulate storage at elevated For markedly improved scratch and
temperature abrasion resistance, approx 5 to 10%
Moderately polar solvents such as xylene nanoparticles by weight of the solids in
or toluene should not be used alone in to specify a shelf-life (using the a formulation are required this corre-
formulations. These solvents are, how- Arrhenius principle that reaction rates sponds to 20% NANOCRYL and
ever, in general very compatible when roughly double for a 10C increase in NANOPOL or 25% NANOPOX
used in blends with popular solvents such temperature). because the silica nanoparticle content
as esters, ketones and alcohols. differs depending on the form supplied.
To save laboratory time when developing
Certain additives can result in incompati- coatings with silica-nanocomposites,
bilities with silica-nanocomposites. These compatibility lists are available on request
manifest themselves in, for example, for the additives most commonly used
agglomeration, flocculation or increased with NANOCRYL, NANOPOX and
viscosity of the coating formulation. NANOPOL.

Technical Background_Silica-Nanocomposites page 153


Nanocryl: products for UV-coatings

SiO2 content Dyn. viscosity,


Type Monomer Characterization [wt%] 25C

Nanocryl C 130 CTFA Trimethylol propane formalacrylate 50 275 mPas

Nanocryl C 140 HDDA Hexanediol diacrylate 50 175 mPas

Nanocryl C 145 TPGDA Tripropylen glycol diacrylate 50 200 mPas

Nanocryl C 150 TMPTA Trimethylol propane triacrylate 50 3,3 Pas

Nanocryl C 153 TMPEOTA Ethox. Trimethylol propane triacrylate 50 1,0 Pas

Nanocryl C 155 GPTA Propox. Glycerine triacrylate 50 1,75 Pas

Nanocryl C 165 PPTTA Alkox. Pentaerythritol tetraacrylate 50 2,5 Pas

Nanopox: products for coatings

SiO2 content EEW Dyn. viscosity,


Type [wt%] Base resin [g/equiv.] 25C [mPas] Characterization

Nanopox C 450 40 DGEBA 295 60,000 aromatic

DGEBA/DGEBF aromatic,
Nanopox C 460 40 290 45,000 cristallizationfree

Nanopox: product for UV-coatings

SiO2 content Dyn. viscosity,


Type Monomer Characterization [wt%] 25C

Cycloaliphatic epoxy resin for


Nanopox C 620 EEC cationic curing 40 4,0 Pas

Nanopol: products for coatings

SiO2 content Dyn. viscosity,


Type Solvent Characterization [wt%] 25C

Nanopol C 764 MPA Methoxypropylacetate 50 20 mPas

Nanopol C 784 n-BA N-Butylacetate 50 20 mPas

page 154 Technical Background_Silica-Nanocomposites


Silica-nanocomposites for various coa- NANOCRYL, a range of silica-nanocom- NANOPOL is a solvent-based product
tings systems posites in various commonly used UV- which is almost universally applicable. It is
curable acrylate monomers, has been equally suited for use in 1-pack stoving
Customized silica-nanocomposites for specially developed for radical-curing UV enamels and in 2-pack PUR or UV coat-
each resin matrix have been developed for coatings. ings.
the different curing mechanisms in coat-
ings. NANOPOX materials are manufactured Other modified products are available on
from epoxide resins and suitable reactive request.
All products are characterized by trans- diluents. Some products can be heat-
parency, low viscosity and easy incorpora- cured anhydrously or room-temperature
tion to the formulation. cured with amines or force cured and
some are suitable for cationic UV curing.

Technical Background_Silica-Nanocomposites page 155


Copyright Airplane: Airbus

page 156 The Big TEGO_Application Fields


Application Fields
Highlights
Selection Tables

The Big TEGO_Application Fields page 157


Architectural Coatings

Alkyd paints (waterborne)

TEGO Dispers 653* TEGO Foamex 883


Solvent-free wetting and dispersing addi- Defoamer concentrate with good compat-
tive. Particularly good wetting and stabili- ibility and excellent long-term effective-
zation of inorganic pigments and fillers. ness in waterborne alkyd paints. Excellent
Also recommended for organic pigments. gloss retention.

TEGO Dispers 656* TEGO VariPlus DS 50


Solvent-free wetting and dispersing addi- Co-binder based on a polyurethane-
tive. Particularly good wetting and stabili- polyol used to improve paint properties.
zation of inorganic pigments and fillers TEGO VariPlus DS 50 improves adhesion
especially titanium dioxide. Good reduc- of waterborne alkyd paints to various
tion of the grinding viscosity. substrates such as plastic or metal. In this
application, it also prevents formation of
flash rust. Increases hardness without
affecting flexibility.

All our wetting and dispersing additives are APE free.


*

page 158 Highlights_Architectural Coatings


Emulsion-based coatings (silk to matte)

TEGO Dispers 715 W* TEGO Foamex K 7 ior during roller application or increase
Universal wetting and dispersing additive Silicone-free defoamer concentrate based brush resistance. Little effect on wet
for inorganic pigments and fillers for the on mineral oil and free of aromatics. abrasion resistance.
production of waterborne coatings. Effective defoamer for paints with PVCs
Strong reduction of grinding viscosity and in the range 30 - 80%. Suitable for emul- TEGO ViscoPlus 3010**
utmost viscosity stability of the resulting sion, silicone resin and silicate paints. Polyurethane thickener with Newtonian
coatings. properties and very high efficiency in the
TEGO Foamex K 8 high shear region. Especially suitable for
TEGO Foamex 1488 Defoamer concentrate based on renewa- adjusting the ICI viscosity. Particularly
Highly efficient defoamer emulsion with ble raw material as an alternative to min- recommended as co-thickener to reduce
good compatibility in many binders over eral oil defoamers. Combines high effi- spattering behavior during roller applica-
a wide range of PVCs. Ideal for use in the ciency with the best possible compatibility tion or to increase brush resistance. Little
letdown. over a wide range of PVCs. Suitable for effect on wet abrasion resistance.
use in paint formulations based on the
TEGO Foamex 8050 commonly-used binders and especially in TEGO ViscoPlus 3030**
Highly effective defoamer concentrate for styrene/acrylic based emulsion paints. Polyurethane thickener with pseudoplas-
waterborne paint systems based on a tic rheology. Recommended as co-thick-
wide variety of binders such as styrene/ TEGO ViscoPlus 3000** ener to reduce spattering behavior during
acrylic, acrylic and terpolymers. Also, Polyurethane thickener with Newtonian roller application or increase brush resist-
excellent for defoaming pigment concen- properties. Particularly recommended as ance. Little effect on wet abrasion resist-
trates. TEGO Foamex 8050 is formu- co-thickener to reduce spattering behav- ance.
lated so it is highly effective and has good
compatibility.

TEGO Foamex 855


Highly effective defoamer emulsion.
Eliminates foam during manufacture and
application. Especially recommended for
styrene acrylic and vinyl acetate based
systems in the PVC ranges of 40 to 80%.

TEGO Foamex 883


Highly effective defoamer concentrate
with excellent long-term effectiveness.
Offers very efficient defoaming for paints
based on vinyl acetate copolymers over a
wide range of PVCs. Recommended for
the mid- to high-PVC range in styrene/
acrylic and acrylic systems.

All our TEGO ViscoPlus products are VOC and APE free.
**

Manfactured without addition fo organotin compounds.

Highlights_Architectural Coatings page 159


Emulsion-based coatings

TEGO Dispers 715 W* TEGO Foamex 8050 the millbase. The defoaming and the
Universal wetting and dispersing additive Highly effective defoamer concentrate for deaerating effect can be optimized by the
for inorganic pigments and fillers for the waterborne coating systems based on var- use of TEGO Foamex 810 in the mill-
production of waterborne coatings. ious binders such as styrene/acrylic, base.
Strong reduction of grinding viscosity and acrylic and terpolymers. Also excellent for
utmost viscosity stability of the resulting defoaming pigment concentrates. TEGO TEGO Foamex 823
coatings. Foamex 8050 is highly effective while Universally suitable and highly effective
still maintaining good compatibility. defoamer emulsion with good compatibil-
TEGO Dispers 755 W* ity. Easy to incorporate in the let-down.
Highly effective pigment wetting and dis- TEGO Foamex 810 Very good long-term effect.
persing additive for inorganic and organic Highly compatible defoamer concentrate
pigments. Very good color and storage with good effectiveness. Especially rec- TEGO VariPlus DS 50
stability. Good compatibility with pigment ommended as a millbase defoamer for Co-binder based on a polyurethane-
pastes. Little effect on water resistance or sensitive paint formulations. Can also be polyol for improving coating properties.
wet abrasion resistance of the coating. added to clear coats and to the letdown. TEGO VariPlus DS 50 improves adhesion
on various substrates such as plastic or
TEGO Foamex 1488 TEGO Foamex 815 N metal. It also prevents formation of flash
Defoamer emulsion with very high effi- Defoamer emulsion with good effective- rust, and increases hardness and block
ciency and good compatibility without ness and excellent compatibility without resistance.
impairing gloss. Universal defoamer for impairing gloss. Easy to incorporate at the
use in the millbase and letdown. letdown stage but also suitable for use in

All our wetting and dispersing additives are APE free.


*

page 160 Highlights_Architectural Coatings


TEGO ViscoPlus 3000** TEGO ViscoPlus 3030** TEGO ViscoPlus 3060**
Polyurethane thickener with Newtonian Polyurethane thickener with pseudoplas- Polyurethane thickener with strong pseu-
properties. Recommended for adjusting tic rheology. Recommended for adjusting doplastic rheology. Especially suitable for
application viscosity. Reduces roller spat- in-can viscosity. Prevents sedimentation applying thick coats in spray application.
ter and increases brush resistance. Good and syneresis. Good compatibility with Positive effect on leveling and gloss.
color acceptance and improves flow and pigment pastes and enhances leveling
gloss. Free from emulsifiers. and gloss.

TEGO ViscoPlus 3010**


Polyurethane thickener with very high
efficiency at high-shear. Especially
suitable for adjustment of ICI viscosity.
Improves spattering, brush resistance
and leveling. Good compatibility with
pigment pastes.

Flooring
(solventborne and solvent-free)
ADDID 230 TEGO Airex 900
Solvent-free antistatic additive based on a Highly effective deaerator concentrate for
quaternary ammonium compound. In solventborne and solvent-free coatings
larger quantities very effectively increases based on 2-pack epoxies. Added to the
the conductivity of coatings, even without epoxy resin component. Very effective at
addition of conducting fillers or carbon preventing air inclusions and pinholes.
fibers. No effect on color and therefore
suitable for clear coats. 100 % active sub- TEGO Airex 910
stance. Highly compatible deaerator for solvent-
borne and solvent-free coatings based on
ADDID 240 2-pack epoxies. Easy to incorporate and
Solvent-free antistatic additive based on minimizes tendency of cloudiness in clear
quaternary ammonium compounds. Very coats. Silicone-free.
effective increase in conductivity of coat-
ings when used in conjunction with con-
ductive fillers or carbon fibers. No effect
on color and therefore suitable for clear
coats. 100% active substance.

All our TEGO ViscoPlus products are VOC and APE free.
**

Manfactured without addition fo organotin compounds.

Highlights_Architectural Coatings page 161


TEGO Airex 922 TEGO Airex 990 TEGO Dispers 652*
Highly effective silicone- and solvent-free Universal deaerator for two-pack poly- Wetting and dispersing additive for inor-
deaerator for epoxy floor coatings with urethane and epoxy floor coatings. Sol- ganic pigments and titanium dioxide in
very good compatibility. Also suitable for vent-free and suitable for use in coatings solventborne and solvent-free epoxy floor
use in clear epoxy sealants. Satisfies the conforming to AgBB scheme***. coatings. Reduces millbase viscosity and
requirements for coatings conforming to prevents settling of pigments and fillers.
AgBB scheme***. TEGO Dispers 650* Especially suitable for glossy coatings.
Wetting and dispersing additive for
TEGO Airex 940 organic pigments and carbon blacks in TEGO Glide B 1484
Deaerator for solventborne and solvent- solventborne and solvent-free epoxy floor Flow and slip additive with deaerating
free coatings based on 2-pack poly- coatings. Reduces millbase viscosity and properties and good compatibility for sol-
urethanes and epoxies. Excellent prevents settling of pigments and fillers. ventborne and solvent-free 2-pack epoxy-
deaeration, easy incorporation, good Promotes leveling. and polyurethane coatings.
compatibility and excellent overcoata
bility.

TEGO Airex 944


Highly effective, solvent-free deaerator
concentrate with low odor for use in
solventborne and solvent-free 2-pack Flooring (waterborne)
polyurethane and epoxy floor coatings.
Conforms to AgBB scheme***. Good over-
coatability. TEGO Airex 901 W TEGO Airex 902 W
Highly effective deaerator concentrate for Highly compatible deaerator emulsion for
pigmented waterborne coatings based on waterborne coatings based on 2-pack
2-pack polyurethanes and epoxies. Pre- polyurethanes and epoxies. Prevents
vents micro- and macro-foam. Incorpora- micro- and macro-foam. Suitable for pig-
tion requires high shear. mented or non-pigmented systems. Easy
to incorporate.

AgBB: German Committee for Health related Evaluation of


***

Building Products All our wetting and dispersing additives are APE free.
*

page 162 Highlights_Architectural Coatings


TEGO Dispers 650* Hydrophobing
Wetting and dispersing additive for
organic pigments and carbon blacks in
waterborne epoxy floor coatings. Reduces TEGO Phobe 1401 tional water-beading effect. Use in com-
millbase viscosity and prevents settling of Universally applicable hydrophobing bination with special fillers enables paints
pigments and fillers. Promotes leveling. agent for various coating formulations. with a particularly strong water-beading
Outstanding compatibility with commonly effect to be formulated. Further proper-
TEGO Dispers 652* used binders. It produces a noticeable ties of TEGO Phobe 1505 are low VOC.
Wetting and dispersing additive for inor- water-beading effect. When used in sili-
ganic pigments and titanium dioxide in cate paints, the storage stability of the
waterborne epoxy floor coatings. Reduces paints is also improved.
millbase viscosity and prevents settling of
pigments and fillers. Particularly suitable TEGO Phobe 1505
for glossy coatings. Highly concentrated hydrophobing agent
for formulating waterborne exterior
TEGO Wet 240 paints and plasters with water-beading
Substrate wetting additive for improving effect. TEGO Phobe 1505 can also be
substrate wetting of waterborne floor used in combination with a silicone resin
coatings. Leveling is improved particularly to formulate waterborne silicone resin
for 2-pack epoxy formulations. paints and plasters to produce an addi-

Highlights_Architectural Coatings page 163


TEGO Phobe 1650
TEGO Phobe 1650 is a silicone resin
Solventborne architectural paints
emulsion for formulating waterborne sili-
cone resin paints and plasters. Formula-
tions with TEGO Phobe 1650 offer Lipotin DB TEGO Airex 940
excellent protection of the faade from Wetting and dispersing additive for inor- Highly effective deaerator solution for
rain and water. TEGO Phobe 1650 ganic and organic pigments which is also solventborne alkyd paints. Suitable for
offers good protection immediately after suitable for binder-free pastes. Good addition to the millbase or let-down.
the first exposure to rain. Silicone resin compatibility even in low-polarity paint
paints based on TEGO Phobe 1650 are formulations. TEGO Glide 410
very durable and characterized by low dirt Highly active slip and flow agent for sub-
uptake. TEGO Phobe 1650 is cost effec- TEGO Airex 944 strate wetting and prevention of craters.
tive and therefore offers advantages over Highly effective deaerator concentrate for In solventborne paints, very low concen-
established commercial products. high solids, solventborne alkyd paints for trations suffice to achieve excellent slip
addition to the millbase. Incorporation properties.
requires high shear.
TEGO VariPlus TC
TEGO Airex 931 Synthetic resin for improving paint prop-
Universal deaerator for high solids, sol- erties such as good pigment wetting.
ventborne alkyd and acrylic paints with Additionally, TEGO VariPlus TC improves
good compatibility. Suitable for adding to adhesion of solventborne paints on sub-
the let-down and for use in clear coats. strates such as plastics and metals. Espe-
cially good at increasing the hardness
without reducing the flexibility. TEGO
VariPlus TC can prolong the drying time
of alkyd paints.

page 164 Highlights_Architectural Coatings


Printing Inks

Solventborne inks and varnishes TEGO Glide 410


Very strong slip additive. Especially
recommended for pigmented inks.
TEGO Airex 900 TEGO Dispers 670*
Highly effective deaerator concentrate for High performance dispersing additive for TEGO Glide 450
solventborne flexo and gravure printing solventborne formulations. The millbase Universal flow and slip additive. Despite
inks. Effectively prevents micro- and viscosity is strongly reduced making pos- maximum effectiveness, very good
macro-foam and destroys existing foam. sible a high pigment loading during grind- reprintability and thus suitable for print-
Solvent-free. ing. TEGO Dispers 670 is suitable for ing inks and overprinting varnishes.
numerous organic, inorganic and carbon Solvent-free.
TEGO Airex 931 black pigments and leads in particular to
Deaerator for slightly to highly polar coat- high color strength development and TEGO Glide A 115
ings. Very high effectiveness and thus transparency. Highly effective slip and anti-scratch addi-
used at low addition levels. tive. Excellent flow and synergistic effects
TEGO Foamex N with waxes. Ideal for cellulose nitrate and
Extremely effective deaerator concentrate polyamide-based formulations.
for solventborne and radiation-curing pig-
mented printing inks. Ensures extremely
rapid deaeration and breaks foam bub-
bles. Especially recommended for screen
printing application. Solvent-free.
All our wetting and dispersing additives are APE free.
*

Highlights_Printing Inks page 165


TEGO VariPlus SK Solventborne Litho(offset) and
Co-binder to achieve better adhesion of
printing inks on difficult substrates. This
inkjet inks letterpress printing inks
hard resin is based on a special polyol. It
improves the mechanical and chemical
resistance while also improving the gloss TEGO Dispers 670* TEGO Glide A 115
and lowering the viscosity. TEGO High performance dispersing additive for Highly effective slip, antiblocking and
VariPlus SK increases the color strength solventborne formulations. The millbase anti-scratch additive. Provides synergistic
and shows broad solubility and compati- viscosity is strongly reduced making pos- effects with waxes.
bility in solventborne printing inks. sible a high pigment loading during grind-
Contains no solvents. ing. TEGO Dispers 670 is suitable for
numerous organic, inorganic and carbon
TEGO VariPlus TC black pigments and leads in particular to
Special synthetic resin to improve the pig- high color strength development and
ment wetting and stabilization. When transparency.
used in the grinding stage, the benefits
are strongly improved pigment wetting TEGO Glide 410
and higher gloss of the finished ink. This Surface active multifunctional additive,
product is recommended for various sys- which modifies and improves the droplet
tems including nitrocellulose-based print- formation, substrate wetting and mechan-
ing inks. Broad solubility in different sol- ical resistance. TEGO Glide 410 can be
vents, TEGO VariPlus TC is solvent-free. used in standard and eco-solvent ink jet
formulations.

All our wetting and dispersing additives are APE free.


*

page 166 Highlights_Printing Inks


Radiation-curing overprint varnishes

TEGO Airex 920 TEGO Glide 432 TEGO Rad 2500


Highly compatible deaerator for UV over- Extremely effective slip, flow and sub- Radical cross-linkable, highly effective
print varnishes and pigmented printing strate wetting additive. Can be used slip additive. Improves scratch-resistance
inks. Effectively eliminates micro-foam almost universally. Ideally suited for and deaeration. Solvent-free. Particularly
without creating surface defects or creat- radiation-curing overprint varnishes on suitable for matt and high-viscosity over-
ing overprint problems. Recoatable, sili- fresh offset inks. Solvent-free. print varnishes.
cone- and solvent-free.
TEGO Rad 2010 TEGO Wet 270
TEGO Dispers 652* Novel, radical cross-linkable slip- and Reprintable and glueable substrate wet-
Wetting and dispersing additive for inor- substrate wetting additive with excellent ting additive. Excellent reduction of static
ganic pigments and matting agents. Very price performance ratio. TEGO Rad surface tension, prevention of craters.
suitable for radiation-curing printing inks 2010 is low foaming to defoaming and Solvent-free.
and varnishes. Solvent-free. improves the leveling. Solvent-free.

TEGO Flow 370 TEGO Rad 2011


Silicone-free flow and leveling additive Novel, radical cross-linkable leveling and
based on polyacrylate chemistry. The sur- substrate wetting additive with excellent
face remains heat-sealable, bondable and price performance ratio. TEGO Rad
overprintable. The surface tension is not 2011 is defoaming, highly compatible and
affected by TEGO Flow 370. reprintable. Solvent-free.

Highlights_Printing Inks page 167


Radiation-curing flexo, silk screen and
offset inks

TEGO Airex 900 TEGO Flow 370


Highly effective deaerator concentrate. Silicone-free flow and leveling additive
Ensures rapid deaeration and good flow. based on polyacrylate chemistry. The sur-
Especially for pigmented silk screen inks. face remains heat-sealable, bondable and
overprintable. The surface tension is not
TEGO Airex 920 affected by TEGO Flow 370.
Highly compatible deaerator for UV over-
print varnishes and pigmented printing TEGO Foamex N
inks. Effectively eliminates micro-foam Defoamer concentrate for extremely
without affecting the surface or causing powerful defoaming and deaeration of
overprint problems. Glueable, silicone- pigmented, radiation-curing printing inks.
and solvent-free.
TEGO Glide 435
TEGO Dispers 656* Low-foam slip and flow additive with
Wetting and dispersing additive for inor- excellent substrate wetting. Highly effec-
ganic pigments and fillers, especially for tive and solvent-free.
titanium dioxide. Effectively reduces the
viscosity of the grind and the ink. Can
also be used as combination additive to
reduce viscosity with critical organic pig-
ments. Solvent-free.

All our wetting and dispersing additives are APE free.


*

page 168 Highlights_Printing Inks


TEGO Rad 2010 Radiation-curing inkjet inks
Novel, radical cross-linkable slip- and
substrate wetting additive with excellent
price performance ratio. TEGO Rad TEGO Airex 920 TEGO Rad 2200 N
2010 is low foaming to defoaming and Silicone-free deaerator for compatible Highly compatible, radically crosslinkable
improves the leveling. Solvent-free. defoaming in the production or in the additive. Modifies drop formation,
printing process. 100% active matter reduces surface tension and increases
TEGO Rad 2011 scratch resistance.
Novel, radical cross-linkable leveling and
substrate wetting additive with excellent
price performance ratio. TEGO Rad
2011 is defoaming, highly compatible and
reprintable. Solvent-free.

TEGO Rad 2500


Radiation-curing additive with a unique
set of properties: slip effect, scratch-
resistance and deaeration. Solvent-free.

TEGO Rad 2700


Radiation-curing release additive with
excellent release effect, TEGO Rad 2700
simultaneously increases scratch resist-
ance and promotes deaeration. Limited
suitability for clears.

TEGO VariPlus AP
Polyol-based co-binder works as combi-
nation partner with radiation-curing for-
mulations. TEGO VariPlus AP improves
adhesion, pigment wetting and increases
the curing speed.

Highlights_Printing Inks page 169


Waterborne overprint varnishes

TEGO Airex 902 W TEGO Foamex 842


Deaerator-emulsion, combines high Highly effective defoamer solution.
effectiveness against micro and macro- Easy to incorporate, high gloss retention.
foam with very good compatibility. When the defoamer-containing varnish is
Very good long-term stability. stored, the defoaming effect is maintained
for a long time.
TEGO Foamex 805 N
Solid-particle-free defoamer emulsion TEGO Foamex 845
with excellent compatibility. Ideal for Highly effective defoamer emulsion with
effectively defoaming coating formula- very good long-term effectiveness. Highly
tions susceptible to surface defects. effective at preventing foam formation,
destroys existing foam. Defoams even
TEGO Foamex 831 overprint varnishes with high surfactant
Silicone-, solvent- and mineral oil-free content without affecting the gloss.
defoamer with long lasting effect for use
in the grind or the let-down. In compli- TEGO Glide 410
ance with all relevant European food Excellent slip and flow additive. TEGO
regulatory ordinances. Glide 410 increases scratch-resistance,
mar-resistance and improves flow without
any negative effects on the gloss.
Solvent-free.

page 170 Highlights_Printing Inks


TEGO Glide 482 Waterborne flexo and gravure inks
Highly effective slip and anti-blocking
additive. Increases scratch resistance and
improves slip characteristics in clear and
matte formulations. TEGO Airex 901 W TEGO Dispers 760 W*
Deaerator concentrate with high effi- Highly effective wetting and dispersing
TEGO Twin 4000 ciency against micro-foam. Highly suita- additive particularly for grinds with bind-
Siloxane gemini surfactant with distinct ble as defoamer for the grind. Easy to ers for waterborne flexo and gravure inks.
defoaming properties and powerful sur- combine with defoamer emulsions in the Gives high gloss and color strength and
face tension reduction. This unique prod- let-down. Solvent-free. allows high pigment contents without
uct distinguishes itself by outstanding thixotropy. Ideal for carbon blacks and
substrate wetting, foam inhibition and TEGO Dispers 653* organic pigments.
fast foam collapsing. Even suitable for Very versatile wetting and dispersing
wetting on fresh litho offset prints. additive for grinds with or without bind- TEGO Dispers 765 W*
Solvent-free. ers for waterborne flexo and gravure inks. Polymeric high-performance wetting and
Highly compatible with various let-down dispersing additive for waterborne print-
TEGO Wet 510 vehicles. Suitable for all types of pig- ing inks. Especially recommended for the
Dynamic substrate wetting additive with ments, ideal for phthalocyanine and inor- formulation of binder-free pigment con-
excellent flow-promoting properties. ganic pigments. centrates. Suitable also for binder con-
Improves gloss and is easy to incorporate. taining grinds. Excellent reduction of vis-
Silicone- and solvent-free. cosity, outstanding stabilization of organic
and inorganic pigments and very good
color development.

All our wetting and dispersing additives are APE free.


*

Highlights_Printing Inks page 171


TEGO Foamex 810 TEGO Foamex 842 TEGO Glide 482
Highly effective defoamer concentrate Highly effective defoamer solution. Can Highly effective slip and anti-blocking
with minimal risk of surface defects. be used in the grind and/or the let-down. additive. Increases scratch resistance and
Excellent for multi-use pigment grinds, as Easy to incorporate. When used as grind- improves slip characteristics in clear and
a grind defoamer and also in the let-down ing stage defoamer TEGO Foamex 842 matte formulations.
of many flexo and gravure inks. can ideally be combined with defoamer
Solvent-free. emulsions (e.g. TEGO Foamex 845) at TEGO Twin 4100
the let-down stage. When the defoamer- Siloxane gemini surfactant with effective
TEGO Foamex 822 containing ink is stored, the defoaming surface tension reduction and defoaming
High compatible defoamer emulsion. effect is maintained for a long time. properties. This unique product distin-
Unique in that it is highly effective while guishes itself by outstanding substrate
also very compatible with long-lasting TEGO Foamex 843 wetting on various print stocks, excellent
effect. Ideal for use in the let-down and Defoamer compound for a fast foam compatibility and fast foam collapsing.
for subsequent addition to the ink. knock-down and foam inhibition. Very Solvent-free.
high effectiveness, combined with excel-
TEGO Foamex 831 lent compatibility. Ideal for addition at the TEGO ViscoPlus 3000
Silicone-, solvent- and mineral oil-free let-down stage. Superior long-term effec- Polyurethane thickener with newtonian
defoamer with long lasting effect for use tive. Especially designed for low viscous rheology for adjustment of rheology for
in the grind or the let down. In compli- formulations based on acrylics and sty- the printing process. High color develop-
ance with all relevant European food reg- rene acrylics. ment. Reduced penetration in strong
ulatory ordinances. absorbent substrates. Free of emulsifiers,
TEGO Foamex 845 solvents and APE. Produced without use
Highly effective defoamer emulsion with of tin-organic substances.
very good long term effectiveness. Espe-
cially recommended for use in the let-
down. Effectively prevents foam forma-
tion and destroys existing foam.

page 172 Highlights_Printing Inks


TEGO Wet 500 TEGO Wet 505
Foam inhibiting wetting agent with good Dynamic substrate wetting additive with
dynamic properties. Improves wetting of significant degassing effect. Improves pig-
a wide variety of different substrates and ment wetting and remains highly reprint-
pigment surfaces, without side-effects. able. Ideal for use in the grind. Silicone
Silicone and solvent-free. and solvent-free.

Waterborne inkjet inks

TEGO Dispers 755 W* TEGO Foamex 805 N TEGO Wet KL 245


High-performance wetting and dispersing High-perfomance defoamer with good Fully water soluble surfactant based on
additive for stabilization of organic pig- compatibility. Well suited for use in the polyethersiloxane technology. Achieves
ments and carbon blacks. Strongly production process and in circulation good substrate wetting on difficult sub-
reduces the viscosity and leads to more inkjet systems. strates like films. It can also be used to
Newtonian flow behavior. support the wetting of pigments in the
TEGO Glide 440 grinding stage.
TEGO Dispers 760 W* Positively Influences the droplet forma-
Reduction of viscosity and improvement tion and substrate wetting of waterborne
of color strength are special properties of inkjet inks. Improves the mechanical
TEGO Dispers 760 W. It is well suited resistance.
for carbon black and organic pigments.

All our wetting and dispersing additives are APE free.


*

Highlights_Printing Inks page 173


Wood, Furniture and
Parquet Coatings

Solventborne wood and furniture coatings

TEGO Airex 910 TEGO Airex 936


Highly compatible deaerator for coatings Highly effective, silicone-free deaerator
based on unsaturated polyesters. Also for top coats and primers. Especially suit-
suitable for curtain coater application. able for 2-pack polyurethane and acid-
curing coatings as well as coatings based
TEGO Airex 931 on nitrocellulose. Recommended for
Effective deaerator with good compatibil- spray and roller application.
ity. Ideally suitable for spray applied,
2-pack polyurethane coating formula- TEGO Airex 990
tions. Suitable for high gloss, matte, pig- Efficient deaerator with very good com-
mented and non pigmented wood and patibility. Excellently suited for use in
furniture coatings. conventional, solventborne and high sol-
ids 2-pack PU formulations. Universally
applicable for all application processes.
Solvent-free.

page 174 Highlights_Wood, Furniture and Parquet Coatings


TEGO Dispers 610* TEGO Flow 425 TEGO VariPlus CA
Controlled flocculating wetting and dis- Highly effective and compatible flow con- Co-binder used to enhance gloss, hard-
persing additive especially for inorganic trol additive. Recoatable, thus recom- ness and body especially in solventborne
pigments and fillers. Excellent for formu- mended not only for top coats but also for NC coatings. The 100% pure ketone-
lating primers, fillers and top coats. Suita- primers and fillers. aldehyde synthetic resin is free of solvent
ble for a very wide range of binders. and tin.
TEGO Glide 406
TEGO Dispers 656* Universal slip additive for top coats and TEGO VariPlus SK
Wetting and dispersing additive for inor- primers. Good recoatability and flow pro- Co-binder to increase gloss and body of
ganic pigments especially transparent iron motion. solventborne 2-pack PU and NC coatings.
oxide pigments. Improves wetting, stabili- The hard resin, based on a special polyol,
zation and transparency of the pigments TEGO Glide 410 also improves the dry time in 2-pack PU
in solventborne coating formulations. Ide- Extremely effective slip additive. High coatings. Free of solvents and tin.
ally suitable for the production of binder- surface slip and scratch resistance and
containing, aromatic-free pigment con- anti-blocking characteristics at very low
centrates. concentrations. In matte coatings, it also
ensures optimum orientation of the mat-
TEGO Dispers 710* ting agent.
Polymeric wetting and dispersing additive
especially suitable for organic pigments
and carbon blacks. Very good pigment
stabilization and color development. Usa-
ble in high to medium polarity formula-
tions and also recommended for inorganic
pigments.

Tego Dispers 670*


High performance dispersing additive for
solventborne formulations. The millbase
viscosity is strongly reduced making pos-
sible a high pigment loading during grind-
ing. TEGO Dispers 670 is suitable for
numerous organic, inorganic and carbon
black pigments and leads in particular to
high color strength development and
transparency.

All our wetting and dispersing additives are APE free.


*

Highlights_Wood, Furniture and Parquet Coatings page 175


Solventborne wood parquet Radiation-curing wood
and floor coatings and furniture coatings

TEGO Airex 931 TEGO Flow 425 TEGO Airex 900


Effective deaerator with good compatibil- Highly effective and compatible flow con- Highly effective deaerator concentrate for
ity. Ideal for use in 1-pack alkyd/urethane trol additive. Recoatable, thus recom- coatings based on acrylate oligomers.
formulations. mended not only for top coats but also for Recommended for roller application.
primers. Incorporation at high-shear is recom-
TEGO Airex 936 mended.
Highly effective, silicone-free deaerator TEGO Glide 100
for top coats, base coats and primers. Combines very good flow properties and TEGO Airex 910
Highly suitable for 2-pack polyurethane-, surface smoothness. Does not impair Highly compatible deaerator for coatings
acid catalysed or nitrocellulose coatings. recoatability. based on unsaturated polyesters and
Recommended for spray and roller appli- acrylic oligomers. Highly suitable for cur-
cation. TEGO VariPlus SK tain coater and vacumat application.
Co-binder to improve gloss and body of
TEGO Airex 990 solventborne 2-pack PU and NC coatings. TEGO Airex 920
Efficient deaerator with very good com- The hard resin, based on a special polyol, Highly compatible universal deaerator for
patibility. Excellently suited for use in also improves the dry time in 2-pack PU top coats and primers based on acrylate
conventional, solventborne and high sol- coatings. Free of solvent and tin. oligomers. Silicone-free. Suitable for cur-
ids 2-pack PU formulations. Universally tain coating, roller application and spray
applicable for all application processes. application.
Solvent-free.
TEGO Dispers 688*
Ideal wetting and dispersing additive for
wetting the surface of matting agents thus
lowering the viscosity of highly filled for-
mulations. Yield point and thixotropy are
reduced which results in improved flow
and easier degassing of the coating.

All our wetting and dispersing additives are APE free.


*

page 176 Highlights_Wood, Furniture and Parquet Coatings


TEGO Dispers 656* TEGO Glide 440 TEGO Rad 2200 N
Wetting and dispersing additive for inor- Highly effective slip additive with minimal Radically crosslinkable, highly compatible,
ganic pigments and fillers, especially for tendency to cause turbidity. Particularly slip additive for increasing the surface
titanium dioxide. Effectively reduces the suitable for glossy top coats. Improves smoothness and the scratch resistance of
grinding viscosity. 100 % active matter, substrate wetting, scratch resistance and top coats. Substrate wetting, scratch
solvent-free. leveling. resistance and flow are all improved.

TEGO Glide 100 TEGO Rad 2010 TEGO Rad 2500


Highly effective and compatible flow con- New type of radically cross-linking slip Radically crosslinkable slip additive and
trol additive. Recoatable, thus recom- and substrate-wetting additive with excel- deaerator. In addition to the deaerating
mended not only for top coats but also for lent price/performance ratio. It destroys effect, surface smoothness, scratch resist-
primers and fillers. foam and promotes flow. ance and block resistance of the coating
are improved.
TEGO Glide 435 TEGO Rad 2011
Low foaming slip and flow additive with New type of radically cross-linking flow
excellent substrate wetting. Promotes ori- additive with excellent price/perform-
entation of matting agents. Ideally suited ance ratio. Highly compatible and recoat-
to formulating matte top coats. able and therefore well suited for primers
and fillers. In top-coat formulations it is
an ideal partner for TEGO Rad 2200 N
and TEGO Rad 2500.

Highlights_Wood, Furniture and Parquet Coatings page 177


Radiation-curing wood parquet and Waterborne wood and
floor coatings furniture coatings
TEGO Airex 900 TEGO Rad 2500 TEGO Airex 901 W
Highly effective deaerator concentrate for Radically crosslinkable slip additive and Highly effective deaerator concentrate for
coatings based on acrylate oligomers. deaerator. In addition to the deaerating combating micro-foam. Particularly suited
Especially for roller application. High- effect, surface smoothness, scratch resist- for airless/airmix application coatings
shear incorporation is recommended. ance and block resistance of the coating based on acrylate emulsions. Outstand-
are improved. ingly effective in high build coatings.
TEGO Airex 920
Highly compatible deaerator for top coats TEGO Wet 270 TEGO Airex 902 W
and primers based on acrylate oligomers. Highly effective anti-crater additive. Universal, compatible deaerator emulsion
Silicone-free. Suitable for curtain coater Recoatable, thus also suitable for primers for removing micro- and macro-foam.
and roller application. and fillers. Also for waterborne 2-pack polyurethane,
radiation curing and alkyd resin emulsion
TEGO Rad 2011 TEGO Dispers 688* based formulations. Suitable for airless/
New type of radically cross-linkable flow Ideal wetting and dispersing additive for airmix application. Also for curtain coat-
additive with excellent price/perform- wetting the surface of matting agents thus ing application.
ance ratio. Highly compatible and recoat- lowering the viscosity of highly filled for-
able and thus well suited for primers. In mulations. Yield point and thixotropy are TEGO Airex 904 W
top coats it forms an ideal partner for reduced which results in improved flow Efficient deaerator concentrate for effec-
TEGO Rad 2500. and easier degassing of the coating. tive elimination of microfoam. High per-
formance combined with excellent com-
patibility. Especially recommended for
airless/airmix application. Also effective
in waterborne radiation-curing and
2-pack polyurethane formulations.

All our wetting and dispersing additives are APE free.


*

page 178 Highlights_Wood, Furniture and Parquet Coatings


TEGO Dispers 752 W* TEGO Foamex 810 TEGO Foamex 843
Wetting and dispersing additive highly Defoamer concentrate with high effec- Defoamer compound for rapid defoaming
recommended for transparent iron oxide tiveness, even against micro-foam, with and effective foam break-down and inhi-
pigments. Suitable for pigment concen- minimal risk of defects. Outstanding bition especially in low-viscosity formula-
trate production and direct grinding. Com- millbase defoamer. Can be used alone or tions. Good long-term effectiveness.
patible with a broad range of binders. in combination with defoamer emulsions.
Also suitable for curtain coating. TEGO Glide 110
TEGO Dispers 755 W* Excellent anti-cratering additive that also
Universal wetting and dispersing additive TEGO Foamex 825 improves flow and surface smoothness.
for organic and inorganic pigments. Universal defoamer emulsion for use in Very compatible and universally applic
Highly suitable for direct grind in the let down and clear coats. Can be used able in waterborne, solventborne and
binder. Particularly suited for manufactur- alone or in combination with TEGO radiation-curing wood and furniture
ing binder-free or binder-containing pig- Foamex 810. Suitable for curtain coater finishes.
ment concentrates. application.
TEGO Glide 410
TEGO Foamex 805 N TEGO Foamex 845 Extremely effective slip additive. High
Defoamer emulsion. Good effectiveness Effective defoamer emulsion with an surface slip and scratch resistance and
with minimal risk of defects. Well suited excellent foam break-down. Also ideal in anti-blocking properties at low concen
to very low viscosity and defect suscepti- combination with TEGO Airex 901 W or trations. In matte coatings, it also ensures
ble formulations. Ideal as a defoamer for TEGO Airex 902 W to combat macro- optimum orientation of the matting agent.
adding to the curtain coating machine. foam.
TEGO Glide 482
Highly effective anti-blocking additive.
Improves scratch resistance and slip in top
coats.

Highlights_Wood, Furniture and Parquet Coatings page 179


TEGO Twin 4100 Good compatibility with pigment pastes. TEGO ViscoPlus 3060**
Siloxane, multi-functional additive for Enhances flow and gloss. Free from emul- Polyurethane thickener with strong pseu-
effective reduction of surface tension. sifiers. doplastic rheology. Performance inde-
Very good substrate wetting and flow pendent of pH. Highly recommended for
promotion with high compatibility. Ideal TEGO ViscoPlus 3010** vertical application of thick films by spray-
for use as an anti-crater additive while Polyurethane thickener with very high ing (e.g. window frames). Promotes lev-
providing a foam neutral to defoaming efficiency in the high-shear region and a eling and gloss. Good storage stability.
environment. Suitable for combination property profile independent of pH.
with defoamers and deaerators. Especially suitable for adjusting the ICI TEGO Wet 270
Solvent-free. viscosity. Additionally has good compati- Highly effective anti-cratering additive.
bility with pigment pastes. Enhances flow Promotes flow and assists pore wetting.
TEGO VariPlus DS 50 and gloss. Recoatable, thus also suitable for primers
Co-binder for improving various coating and fillers.
properties. This aqueous dispersion of a TEGO ViscoPlus 3030**
polyurethane-polyol improves mechanical Polyurethane thickener with pseudoplas- TEGO Wet 505
properties such as hardness and block tic rheology. Performance independent of Silicone-free, highly compatible wetting
resistance in waterborne coating systems. pH. Recommended for reducing sedimen- additive for wetting wood substrates and
Shortens dry time and at the same time tation and syneresis. Good compatibility pigments. Provides degassing effect or
improves gloss. Solvent-free. with pigment pastes and positive effect minimal foam stabilization. High dosing
on leveling and gloss. Good storage sta- tolerance as no undesirable side effects
TEGO ViscoPlus 3000** bility. occur. Can be added at the curtain coater.
Polyurethane thickener with Newtonian
properties and property profile which is
independent of pH. Recommended for
adjusting the application viscosity.

All our TEGO ViscoPlus products are VOC and APE free.
**

Manfactured without addition fo organotin compounds.

page 180 Highlights_Wood, Furniture and Parquet Coatings


Waterborne wood parquet and floor coatings

TEGO Foamex 822 TEGO VariPlus DS 50 TEGO ViscoPlus 3030**


Effective and easy-to-incorporate Co-binder for improving several paint Polyurethane thickener with pseudoplas-
defoamer emulsion for clear coats based properties. This aqueous dispersion of a tic rheology. Performance is independent
on acrylate/polyurethane-copolymer polyurethane-polyol improves mechanical of pH value. Recommended to avoid sep-
emulsions or mixtures of acrylate and properties such as hardness and block aration of waxes and matting agents. High
polyurethane emulsions. Also suitable for resistance in waterborne coating systems. compatibility. Promoting leveling and
waterborne 2-pack PU coatings. High Shortens dry time and improves gloss. gloss.
long-term effectiveness. Solvent-free.
TEGO Wet 270
TEGO Foamex 825 TEGO ViscoPlus 3000** Highly effective anti-cratering additive.
Highly effective defoamer emulsion for Polyurethane thickener with newtonian Promotes flow and assists pore wetting.
clear coats based on acrylate/poly- rheology. Performance is independent of
urethane copolymer emulsion or mixtures pH value. Recommended for adjustment
of acrylate and polyurethane emulsions. of application viscosity. High compatibil-
Can be used alone or in combination with ity. Promoting leveling and gloss. Free of
TEGO Foamex 810. emulsifiers.

TEGO Twin 4100 TEGO ViscoPlus 3010**


Siloxane, multi-functional additive for Polyurethane thickener with very high
effective reduction of surface tension. efficiency in the high-shear region and
Very good substrate wetting and flow performance independent of pH. Particu-
promotion with high compatibility. Ideal larly suitable for adjusting the ICI viscos-
for use as an anti-crater additive while ity. Also good compatibility and improves
providing a foam neutral to defoaming flow and gloss.
environment. Suitable for combination
with defoamers and deaerators.
Solvent-free.

Highlights_Wood, Furniture and Parquet Coatings page 181


Industrial Coatings

Waterborne/thin film

TEGO Airex 902 W Concentrates exhibit excellent color


Highly effective and compatible deaerator intensity and broad compatibility. Espe-
emulsion for eliminating micro- and cially suitable for high-quality applica-
macro-foam in low and medium viscosity tions.
systems based on 2-pack polyurethane
formulations. Suitable for airless/airmix TEGO Dispers 653*
application. Particularly good at stabilizing inorganic
pigments but also suitable for organic pig-
TEGO Dispers 755 W* ments. Pastes exhibit very good compati-
Polymeric solvent-free wetting and dis- bility with waterborne and solventborne
persing additive. Very suitable for inor- formulations. Suitable for aqueous and
ganic and organic pigments as well as glycol-containing pigment pastes. Recom-
fillers and carbon blacks. Outstanding mended for highly pigmented inorganic
reduction in viscosity especially with pigment pastes in combination with
problematical organic pigments. TEGO Dispers 652.

All our wetting and dispersing additives are APE free.


*

page 182 Highlights_Industrial Coatings


TEGO Dispers 656* TEGO Foamex 822 TEGO Flow 425
Universal wetting and dispersing additive Defoamer emulsion combining good Highly effective flow additive with good
for waterborne and solventborne formu- effectiveness with outstanding compati- compatibility. Overcoatable and therefore
lations. Suitable for numerous pigments bility. Particularly suitable for coatings recommended not only for top coats but
and fillers. Particularly suitable for inor- formulations susceptible to defects such particularly for primers and fillers.
ganic pigments, transparent pigments and as those based on polyurethane disper-
aluminum pigments. Promotes gloss and sions. TEGO Glide 450
compatibility in solvent-based formula- Universal flow and slip additive. Despite
tions. TEGO Foamex 843 maximum effectiveness, very good
Defoamer compound for rapid foam col- recoatability and thus suitable for primers
TEGO Dispers 752 W* lapse and effective foam inhibition. Com- and top coats. Solvent-free.
Wetting and dispersing additive well bines excellent effectiveness with good
suited for transparent iron oxide pig- compatibility. Ideal for use in the letdown. TEGO Glide 482
ments. Can be used for manufacture of Outstanding long-term persistence. Par- Highly effective antiblocking additive.
pigment concentrates and direct grind. ticularly suitable for low viscosity acrylic- Increases scratch resistance and slip char-
Compatible with numerous binder sys- and styrene-acrylic-formulations. acteristics in clear and matte formulations.
tems.
TEGO Foamex 810 TEGO Wet 240
TEGO Dispers 741 W* Defoamer concentrate with low tendency Polyethersiloxane affects fine atomization
Economical wetting and dispersing addi- to cause surface defects. Highly effective and defect-free films in waterborne,
tive for direct grind and for water-based, even against micro-foam. Outstandingly spray-applied coating systems even at
binder-free pigment concentrates. Partic- suitable as a millbase defoamer for prim- minimal film thickness. The effectiveness
ularly suitable for organic and inorganic ers, top coats and pigment concentrates. of TEGO 240 is independent of co-sol-
pigments but can also be used for stabiliz- vent content. Solvent-free. Problem-free
ing carbon blacks. The product is manu- recoatable. Optimizes wetting on critical
factured from renewable raw materials. substrates.

TEGO Foamex 805 N


Silica-free, highly compatible defoamer
emulsion, which is very effective but has
minimal tendency to cause defects. Pre-
ferred use in low-viscosity and sensitive
waterborne coating systems such as those
based on polyurethane dispersions.

Highlights_Industrial Coatings page 183


TEGO Wet 500 TEGO VariPlus DS 50
Foam inhibiting wetting additive. Pro- Co-binder based on a polyurethane-
motes the wetting of a wide range of sub- polyol for improving coating properties.
strates and pigments without undesirable Improves adhesion on various substrates
side effects. Highly compatible, recoata- such as plastic or metal. Can increase
ble without any problem and therefore hardness and block resistance.
ideally suited for the use in, e. g. primers,
clear coats and electrodeposition coatings. TEGO AddBond DS 1300
Silicone and solvent-free. Polyester-based co-binder for improving
coating properties. Improves adhesion
TEGO Wet 260 on various substrates such as plastics or
Highly effective substrate wetting addi- metals.
tive for waterborne coating systems. Out-
standingly suited for wetting plastic sub-
strates.

page 184 Highlights_Industrial Coatings


Waterborne/high-build

TEGO Airex 901 W bility with waterborne and solventborne TEGO Dispers 741 W*
Highly effective deaerator concentrate for formulations. Suitable for aqueous and Economical wetting and dispersing addi-
preventing micro-foam. Particularly suita- glycol-containing pigment pastes Recom- tive for direct grind and for water-based,
ble for airless/airmix application. Recom- mended in combination with TEGO binder-free pigment concentrates. Partic-
mended for use in millbase. Dispers 652 for highly pigmented inor- ularly suitable for organic and inorganic
ganic pigment pastes. pigments but can also be used for stabiliz-
TEGO Airex 904 W ing carbon blacks. The product is manu-
Effective deaerator concentrate for elimi- TEGO Dispers 652* factured from renewable raw materials.
nating microfoam. Combines good effec- Co-dispersing additive. Combined with
tiveness with outstanding compatibility. TEGO Dispers 651 improves the rheol- TEGO Dispers 750 W*
Recommended particularly for airless/air- ogy of highly-pigmented inorganic pig- Polymeric, solvent-free wetting and dis-
mix application. Particularly suitable for ment pastes and also improves compatibil- persing additive. Outstanding wetting and
high and medium-low viscosity formula- ity particularly in solventborne coatings. stabilization of inorganic and organic pig-
tions based on acrylic and acrylic/poly- ments as well as fillers. Very good color
urethane dispersions. Also effective in TEGO Dispers 656* strength development and color stability.
waterborne radiation-curing formulations Universal wetting and dispersing additive Concentrates have broad compatibility
as well as 2-pack polyurethane formula- for waterborne and solventborne formu- with a wide variety of aqueous binders.
tions. lations. Suitable for many pigments and Particularly suitable for high-quality appli-
fillers. Particularly suitable for inorganic cations.
TEGO Dispers 653* pigments, transparent pigments and alu-
Particularly good at stabilizing inorganic minum pigments. Promotes gloss and
pigments but also suitable for organic pig- compatibility in solvent-based formula-
ments. Pastes exhibit very good compati- tions.

All our wetting and dispersing additives are APE free.


*

Highlights_Industrial Coatings page 185


TEGO Foamex 810 TEGO Flow 425 TEGO Twin 4100
Defoamer concentrate with low tendency Highly effective flow additive with good Siloxane, multi-functional additive for
to cause surface defects, highly effective compatibility. Overcoatable and therefore effective reduction of surface tension.
even against micro-foam. Outstandingly recommended not only for top coats but Very good substrate wetting and flow
suitable as millbase defoamer for primers, particularly for primers and fillers. promotion with high compatibility. Ideal
top coat and pigment concentrates. for use as an anti-crater additive while
TEGO Glide 450 providing a foam neutral to defoaming
TEGO Foamex 843 Universal flow and slip additive. Despite environment. Suitable for combination
Defoamer compound for rapid foam col- maximum effectiveness, very good with defoamers and deaerators.
lapse and effective foam inhibition. Com- recoatability and thus suitable for primers Solvent-free.
bines excellent effectiveness with good and top coats. Solvent-free.
compatibility. Ideal for use in the let-down. TEGO Wet 270
Outstanding long-term persistence. Par- TEGO Glide 110 Highly effective substrate wetting addi-
ticularly suitable for low viscosity acrylic- Outstanding anti-crater effect and high tive with outstanding anti-crater effect.
and styrene-acrylic formulations. compatibility in waterborne coatings. Promotes flow and is recoatable.
Suitable for pigmented and clear formula-
TEGO Foamex 3062 tions. Promotes good flow, low foaming TEGO Wet 500
Extremely effective defoaming concen- and free of solvents. Foam inhibiting wetting additive. Pro-
trate for the millbase. motes the wetting of a wide range of sub-
TEGO Glide 482 strates and pigments without undesirable
TEGO Foamex K 8 Highly effective antiblocking additive. side effects. Highly compatible, recoata-
Defoamer concentrate based on renewa- Increases scratch resistance and slip char- ble without any problem and therefore
ble raw materials as an alternative to min- acteristics in clear and matte formulations. ideally suited for the use in, e. g. primers,
eral-oil defoamers. Combines high effec- clear coats and electrodeposition coatings.
tiveness with maximum compatibility over Silicone and solvent-free.
a wide range of PVC.
TEGO VariPlus DS 50
Co-binder based on a polyurethane-
polyol for improving coating properties.
Improves adhesion on various substrates
such as plastic or metal. Can increase
hardness and block resistance.

TEGO AddBond DS 1300


Polyester-based co-binder for improving
coating properties. Improves adhesion on
various substrates such as plastics and
metals.

page 186 Highlights_Industrial Coatings


Solventborne/thin film

TEGO Airex 931 TEGO Airex 962 TEGO Dispers 670*


Deaerator for low to high polarity coat- Universal deaerator with good compati- High performance dispersing additive for
ings formulations. Very effective and bility. solventborne formulations. Strongly
therefore only small quantities required. reduces millbase viscosity which permits
Particularly suitable for high solids alkyd TEGO Airex 990 high pigment loading during the grinding
clear coats. Compatible deaerator for conventional process. TEGO Dispers 670 is suitable
clear coats and high-gloss, high solids sys- for numerous organic, inorganic and car-
TEGO Airex 936 tems. Effective against micro- and macro- bon black pigments and leads in particular
Highly effective, silicone-free deaerator foam. Suitable for all spray application to high color strength development and
for top coats and primers. methods. transparency.

TEGO Airex 945 TEGO Dispers 656* TEGO Dispers 710*


Very compatible deaerator for high solids Universal wetting and dispersing additive Polymeric wetting and dispersing additive
clear coats. Additionally promotes flow. for solventborne formulations. Suitable for organic and inorganic pigments. Very
for numerous pigments and fillers. Partic- good development of color intensity and
TEGO Airex 950 ularly suitable for inorganic pigments, good pigment stabilization. Particularly
Highly compatible deaerator for polar, transparent pigments and aluminum pig- effective in high to moderate polarity for-
high solids clear coats. ments. Promotes gloss and compatibility mulations such as 2-pack polyurethane
in solvent-based formulations. coatings. Also suitable for manufacturing
pigment concentrates.

All our wetting and dispersing additives are APE free.


*

Highlights_Industrial Coatings page 187


TEGO Flow 300 TEGO Glide 450 TEGO Twin 4000
Highly compatible polyacrylate with low Universal flow and slip additive. Despite Siloxane multi-functional additive. Highly
tendency to turbidity in solventborne maximum effectiveness, very good effective in reducing surface tension and
coatings, especially in clears. The applied recoatability and thus suitable for primers promoting flow in highly polar systems.
coatings show good flow and high gloss. and top coats. Solvent-free. Solvent-free.
A combination with TEGO Glide 415 or
TEGO Glide 100 promotes brilliant sur- TEGO Wet KL 245 ADDID 900
faces. Additive for improved wetting on con- Amine-modified siloxane for optimizing
taminated substrates. Highly effective adhesion of coatings particularly on
TEGO Flow 370 even at low concentrations. Very good metallic substrates. Especially suitable for
Polyacrylate-based silicone-free flow recoatability and very easy to incorporate. primers.
additive. Produces smooth flow and is
very compatible in solventborne coatings. TEGO Wet 270 TEGO Hammer 501
Particularly suitable for 1-pack and Universal, highly effective substrate wet- High molecular weight polydimethylsi-
2-pack coatings and coil coatings which ting additive with outstanding anti-crater loxane for generating hammertone effects
must satisfy the highest demands with effect. Promotes flow. Solvent-free and particularly in alkyds. Is highly effective
regards to appearance. recoatable. and is used in combination with TEGO
Wet 270 or TEGO Glide 110 to regulate
TEGO Glide 100 TEGO Wet 280 surface texture.
Particularly compatible flow and slip addi- Universal substrate wetting additive with
tive for solventborne and waterborne for- outstanding wetting properties. Particu- TEGO AddBond LTW
mulations. TEGO Glide 100 effectively larly suitable for spray application. Pro- Co-binder for improving adhesion of sol-
prevents contamination craters in solvent- motes flow in high solids coatings. Good ventborne coatings. Soft, flexible polyes-
borne coatings. recoatability and is solvent-free. ter resin.

page 188 Highlights_Industrial Coatings


TEGO VariPlus SK
Co-binder for increasing gloss and body
Solventborne/high-build
of solventborne 2-pack PU and NC coat-
ings. Solvent- and tin-free. TEGO Airex 940 TEGO Airex 991
Deaerator for pigmented, solventborne High performance deaerator for pig-
TEGO VariPlus CA and solvent-free coatings based on 2-pack mented high solids and conventional
Co-binder for increasing gloss, hardness polyurethanes. Also suitable for epoxy coatings. Outstanding effectiveness
and body particularly in solventborne NC systems and high solids alkyds. Easily against micro- and macro-foam even in
lacquers. The 100% ketone-aldehyde incorporated, good compatibility and high-build coatings. Especially suitable
based synthetic resin is solvent- and tin- excellent overcoatability. with airless, airmix and roller application.
free.
TEGO Airex 944 TEGO Foamex N
Deaerator for pigmented, solventborne Extremely effective deaerator concentrate
and solvent-free coatings based on 2-pack for solventborne and solvent-free coat-
polyurethanes, epoxies and high solids ings. Particularly effective in high viscos-
alkyds. Excellent deaeration, easily incor- ity millbase formulations.
porated, good compatibility and excellent
overcoatability. Solvent-free. TEGO Dispers 610*
Co-flocculating wetting and dispersing
TEGO Airex 962 additive for inorganic pigments and fillers.
Universal deaerator with good compati-
bility. TEGO Dispers 700*
Wetting and dispersing additive especially
TEGO Airex 990 for inorganic pigments. Very good pig-
Compatible deaerator for conventional ment wetting and lowering of millbase
clear coats and high gloss, high solids viscosity. Also suitable for manufacturing
systems. Effective against micro- and bentone pastes.
macro-foam. Suitable for all spray appli-
All our wetting and dispersing additives are APE free.
*
cation methods.

Highlights_Industrial Coatings page 189


TEGO Dispers 670* TEGO Flow 425
High performance dispersing additive for Highly compatible polyethersiloxane for
solventborne formulations. Strongly flow promotion. Recoatable.
reduces millbase viscosity which permits
high pigment loading during the grinding TEGO Glide 100
process. TEGO Dispers 670 is suitable for Particularly compatible flow and slip addi-
numerous organic, inorganic and carbon tive for solventborne and waterborne for-
black pigments and leads in particular to mulations. TEGO Glide 100 effectively
high color strength development and prevents contamination craters in solvent-
transparency. borne coatings.

TEGO Dispers 656* TEGO Glide 410


Universal wetting and dispersing additive Additive for improving surface smooth-
for radiation-curing formulations. Suitable ness/slip with substrate wetting proper-
for numerous inorganic pigments and fill- ties. Anti-crater effect.
ers. Reduces viscosity efficiently.
TEGO Glide 450
TEGO Flow 370 Universal flow and slip additive. Despite
Polyacrylate-based silicone-free flow maximum effectiveness, very good
additive. Produces smooth flow and is recoatability and thus suitable for primers
very compatible in solventborne coatings. and top coats. Solvent-free.
Particularly suitable for 1-pack and
2-pack coatings and coil coatings which TEGO Glide B 1484
must satisfy the highest demands with Compatible slip and flow additive with
regards to appearance. deaerating properties for solventborne
and solvent-free 2-pack epoxy and polyu-
rethane coatings.

All our wetting and dispersing additives are APE free.


*

page 190 Highlights_Industrial Coatings


ADDID 900
Amine-modified siloxane for optimizing
UV
adhesion of coatings particularly on
metallic substrates. Especially suitable for TEGO Rad 2010 TEGO Flow 425
primers. New type of radically crosslinkable slip Highly-effective flow additive with high
and substrate wetting additive with excel- compatibility. Overcoatable and therefore
TEGO Hammer 501 lent price/performance ratio. Destroys recommended not only for top coats but
High molecular weight polydimethylsi- foam and promotes flow. Solvent-free. particularly for primers and fillers.
loxane for generating hammertone effects
particularly in alkyds. Is highly effective TEGO Rad 2011 TEGO Glide 432
and is used in combination with TEGO New type of radically crosslinkable flow Universal, highly effective slip, flow and
Wet 270 or TEGO Glide 110 to regulate and wetting additive with excellent price/ substrate wetting additive. Solvent-free.
surface texture. performance ratio. Inhibits foam, very
compatible and overprintable. Solvent- TEGO Airex 920
TEGO AddBond LTW free. Highly compatible deaerator. Eliminates
Co-binder for improving adhesion of sol- micro-foam efficiently without causing
ventborne coatings. Soft, flexible polyes- TEGO Rad 2500 surface defects or problems. Silicone- and
ter resin. Radically crosslinkable, highly effective solvent-free.
slip additive. Improves scratch resistance
TEGO VariPlus SK and is deaerating. Solvent-free. Particu-
Co-binder for increasing gloss and body larly suitable for matte and high-viscosity
of solventborne 2-pack PU and NC coat- coatings.
ings. Solvent- and tin-free.

TEGO VariPlus CA
Co-binder for increasing gloss, hardness
and body particularly in solventborne NC
lacquers. The 100% ketone-aldehyde
based synthetic resin is solvent- and tin-
free.

Highlights_Industrial Coatings page 191


Pigment
Concentrates

Solventborne pigment concentrates

COLOROL F* minium pigments. Improves gloss and


Wetting and dispersing additive for inor- compatibility in solventborne formula-
ganic and organic pigments. Also suitable tions.
for binder-free pigment concentrates and
bentone pastes. Concentrates also have TEGO Dispers 670*
good compatibility with low-polarity High performance dispersing additive for
coatings formulations. solventborne formulations. The millbase
viscosity is strongly reduced making pos-
TEGO Dispers 656* sible a high pigment loading during grind-
Universal wetting and dispersing additive ing. TEGO Dispers 670 is suitable for
for solventborne formulations. Suitable numerous organic, inorganic and carbon
for a wide range of pigments and fillers. black pigments and leads in particular to
Especially recommended for inorganic high color strength development and
pigments, transparent pigments and alu- transparency.

All our wetting and dispersing additives are APE free.


*

page 192 Highlights_Pigment Concentrates


TEGO Dispers 700* Pigment concentrates for UV coatings
Wetting and dispersing additive especially
for inorganic pigments. Very good pig-
ment wetting and reduction of millbase TEGO Dispers 656*
viscosity. Also suitable for the manufac- Universal wetting and dispersing additive
ture of bentone pastes. for radiation-curing formulations. Suita-
ble for a wide range of inorganic pig-
TEGO Dispers 710* ments and fillers. Reduces effectively
Polymeric wetting and dispersing addi- the viscosity. Solvent-free.
tive. Particularly suitable for organic pig-
ments and pigment blacks. Very good
pigment stabilization and development of
color strength. Suitable for medium to
high polarity formulations. Also recom-
mended for inorganic pigments.
Universal concentrates (for solventborne and
waterborne architectural coatings)
TEGO VariPlus TC
Special-purpose ketone-aldehyde con-
densation resin with universal solubility TEGO Dispers 650* TEGO Dispers 653*
and compatibility. Excellent pigment wet- Outstanding stabilization of organic pig- Particularly good stabilization of inorganic
ting when used as a grinding resin for sol- ments. Good color strength and compati- pigments, but also suitable for organic
ventborne coatings. bility of the pigment pastes in waterborne pigments. Very good compatibility of
and solventborne formulations. Recom- concentrates with water and solventborne
mended for aqueous and glycol-based formulations. Suitable for water and gly-
pigment pastes. col-based pigment concentrates. Recom-
mended for highly-pigmented inorganic
pigment concentrates in combination with
TEGO Dispers 652.

Highlights_Pigment Concentrates page 193


TEGO Dispers 652* TEGO Dispers 660 C*
Co-dispersing agent. Combined with Very effective compatibilizer for water-
TEGO Dispers 653, improves rheological borne formulations. Improves the compat-
properties of highly-pigmented inorganic ibility of pigment concentrates in base
pigment concentrates while also improv- paints to reach higher color acceptance
ing compatibility, particularly in solvent- and reduced rub-out value. Also Improves
borne coatings. as co-dispersant the storage stability of
pigment concentrates. Solvent-free.
TEGO Dispers 656*
Universal wetting and dispersing additive TEGO Dispers 662 C*
for solventborne formulations. Suitable Universal compatibilizer for solventborne
for a wide range of pigments and fillers. formulations. Improves the compatibility
Especially recommended for inorganic of pigment concentrates in base paints to
pigments, transparent pigments and reach higher color acceptance and reduced
aluminium pigments. Improves gloss and rub-out value.
compatibility in solventborne formula-
tions.

All our wetting and dispersing additives are APE free.


*

page 194 Highlights_Pigment Concentrates


Waterborne pigment concentrates
TEGO Dispers 650* viscosity especially with problematic which are difficult to wet. In combination
Outstanding stabilization of organic pig- organic pigments. The concentrates have with TEGO Dispers 750 W the best pos-
ments. Very good development of color excellent color strength and broad com- sible depth of color (Jetness) is achievable
strength and compatibility of pigment patibility particularly in high-quality appli- with carbon blacks. Solvent-free.
concentrates. Suitable also for binder- cations such as automotive finishes.
containing pigment concentrates. TEGO VariPlus DS 50
Solvent-free. TEGO Dispers 760 W* Aqueous resin dispersion for the manu-
Recommended for pigment grinding with facture of binder-containing pigment con-
TEGO Dispers 653* binders. Very effective reduction of mill- centrates. Improves gloss, hardness, pig-
Solvent-free wetting and dispersing addi- base viscosity even with high pigment ment wetting, chemical and corrosion
tive. Particularly good wetting and stabili- loading. Especially suitable for pigments resistance of waterborne coatings.
zation of inorganic pigments and fillers.
Also recommended for organic pigments.

TEGO Dispers 741 W*


Economical wetting and dispersing addi-
tive for aqueous, binder-free pigment
concentrates. Particularly suitable for
organic and inorganic pigments but can
also be used for stabilizing carbon blacks.
Based on renewable raw materials.

TEGO Dispers 752 W*


Ideally suitable for transparent iron oxides
and transparent titanium dioxides. Very
high pigment concentrate achievable with
low viscosity. Good storage stability of
the pigment concentrates and excellent
clarity in wood, automotive and industrial
coatings. Solvent-free.

TEGO Dispers 755 W*


Polymeric, solvent-free wetting and dis-
persing additive. Well suited for inorganic
and organic pigments as well as fillers and
carbon blacks. Outstanding reduction in

Highlights_Pigment Concentrates page 195


Co-Binders

Highlights Co-Binders

TEGO VariPlus SK
Hydroxyl-containing, formaldehyde-free
co-binder based on a hydrogenated
ketone-aldehyde resin. The hard resin
character enables hardness, gloss, block
resistance and a faster touch-dry. The
hyper-branched polymer structure lowers
viscosity thus permitting a reduction in
VOC.

page 196 Highlights_Co-Binders


TEGO VariPlus DS 50 Good compatibility with numerous bind-
Aqueous dispersion of a hydroxyl-con- ers. Improves intercoat adhesion in multi-
taining, formaldehyde-free, di-isocyanate coat systems, cohesion in special effect
crosslinked co-binder based on a hydro- coatings, flexibility and gloss.
genated ketone-aldehyde resin. The hard
resin character enables the coatings hard- TEGO AddBond DS 1300
ness, gloss, adhesion, resistance to water Aqueous dispersion of a widely-compati-
and chemicals as well as block resistance ble soft special polyester co-binder used
to be increased. as an adhesion-promoting component for
waterborne formulations on metal and
TEGO AddBond HS plastic substrates. TEGO AddBond DS
Soft, special polyester co-binder used as 1300 improves the flexibility of the
an adhesion-promoting component for a coating.
diverse range of solventborne coatings
and printing inks on numerous substrates
(e.g. metals, plastics and minerals). Well-
suited for use in high solids systems.

Highlights_Co-Binders page 197


Selection Tables

Architectural Coatings, Defoaming


Waterborne formulations

PVC > 40% Addition to the grinding stage Addition to the let-down stage

TEGO Foamex 883 TEGO Foamex 825


TEGO Foamex K 8 TEGO Foamex 845
Styrene acrylics TEGO Foamex 8050 TEGO Foamex 823

TEGO Airex 901 W TEGO Foamex 8030


TEGO Foamex 883 TEGO Foamex 845
Pure acrylics TEGO Foamex 810 TEGO Foamex 825

TEGO Foamex 8050 TEGO Foamex 855


TEGO Foamex 883 TEGO Foamex 1488
Terpolymers/vinyl acetate TEGO Foamex K 8 TEGO Foamex 825

TEGO Foamex 810 TEGO Foamex 815 N


Hybrid systems TEGO Foamex 8050 TEGO Foamex 825

TEGO Foamex 815 N


TEGO Airex 901 W TEGO Foamex 845
2-pack epoxy TEGO Foamex 810 TEGO Airex 902 W

Waterborne formulations

PVC 40% Addition to the grinding stage Addition to the let-down stage

TEGO Foamex 8050 TEGO Foamex 855


TEGO Foamex 810 TEGO Foamex 8030
Styrene acrylics TEGO Foamex K 8 TEGO Foamex 823

TEGO Foamex 825


TEGO Foamex 810 TEGO Foamex 823
TEGO Foamex 883 TEGO Foamex 1488
Pure acrylics TEGO Foamex K 8 TEGO Foamex 815 N

TEGO Foamex 883 TEGO Airex 902 W


TEGO Foamex 8050 TEGO Foamex 825
Terpolymers/vinyl acetate TEGO Foamex K 8 TEGO Foamex 1488

TEGO Airex 904 W TEGO Foamex 822


TEGO Foamex 843 TEGO Foamex 1488
Acrylics-polyurethanes TEGO Foamex 883 TEGO Airex 902 W

TEGO Airex 904 W TEGO Foamex 825


TEGO Foamex 843 TEGO Airex 902 W
Polyurethanes TEGO Foamex 883 TEGO Foamex 822

TEGO Foamex 883 TEGO Foamex 805 N


TEGO Foamex 810 TEGO Foamex 800
Alkyds TEGO Foamex 843 TEGO Foamex 823

TEGO Foamex 815 N TEGO Airex 902 W


2-pack epoxy TEGO Foamex 810 TEGO Foamex 815 N

TEGO Foamex 1488


TEGO Foamex K 3
Bitumen TEGO Foamex K 7

page 198 Selection Tables_Architectural Coatings


Solventborne and solvent-free formulations

Clear and low pigmented Highly pigmented

TEGO Airex 922


TEGO Airex 922 TEGO Airex 900
TEGO Airex 931 TEGO Airex 944
2-pack epoxy, solvent-free TEGO Airex 910 TEGO Airex 940

TEGO Airex 944


TEGO Airex 940 TEGO Airex 940
2-pack PU, solvent-free TEGO Airex 931 TEGO Airex 990

TEGO Airex 931


Acrylics (thermoplastic) TEGO Flow ZFS 460 n.a.

TEGO Airex 944


TEGO Airex 936
Alkyds TEGO Airex 940 n.a.

TEGO Airex 910 TEGO Airex 900


TEGO Airex 940 TEGO Airex 940
2-pack epoxy, solventborne TEGO Glide B 1484 TEGO Foamex N

TEGO Glide B 1484 TEGO Airex 940


TEGO Airex 910 TEGO Foamex 840
2-pack PU, solvenborne TEGO Airex 940 TEGO Airex 990

Selection Tables_Architectural Coatings page 199


Architectural Coatings, Hydrophobing/Primers/
Impregnation

Hydrophobing/Primers/Impregnation

Hydrophobing

Primers/impregnation, solventborne TEGO Phobe 6010

TEGO Phobe 6510


Primers/impregnation, waterborne TEGO Phobe 6600

TEGO Phobe 1401


TEGO Phobe 1500 N
TEGO Phobe 1505
Emulsion paints/plasters TEGO Phobe 1650

TEGO Phobe 1401


TEGO Phobe 1500 N
Emulsion paints/plasters with silicate character TEGO Phobe 1505

TEGO Phobe 1401


TEGO Phobe 1500 N
Silicate emulsion paints TEGO Phobe 1505

TEGO Phobe 1650


Silicone resin paints/plasters TEGO Phobe 1000 S

TEGO Phobe 1401


TEGO Phobe 1500 N
Other coating formulations, waterborne TEGO Phobe 1505

page 200 Selection Tables_Architectural Coatings


Architectural Coatings, Others

Others

Solventborne/-free Waterborne
formulations formulations

Dispersion in the direct grind TEGO Dispers 670 TEGO Dispers 715 W
inorganic pigments TEGO Dispers 656 TEGO Dispers 755 W

TEGO Dispers 670 TEGO Dispers 741 W


organic pigments TEGO Dispers 650 TEGO Dispers 755 W

TEGO Wet KL 245


TEGO Wet 270
Substrate wetting/craters/ TEGO Glide 410 TEGO Wet 500
contaminated substrates TEGO Flow ATF 2 TEGO Wet 265

TEGO Glide 410 TEGO Glide 410


TEGO Glide 450 TEGO Glide 440
Slip/scratch resistance TEGO Glide B 1484 TEGO Glide ZG 400

TEGO ViscoPlus 3000


TEGO ViscoPlus 3030
Leveling/orange peel effect/ TEGO Flow 300 TEGO Wet KL 245
brush marks TEGO Glide 415 TEGO Wet 280

TEGO Glide 410


TEGO Glide B 1484 TEGO Dispers 741 W
Floating/Bnard cells TEGO Flow ATF 2 TEGO Glide 410

TEGO Dispers 662 C TEGO Dispers 660 C


Floating/rub-up/ TEGO Dispers 656 TEGO Dispers 741 W
color stability TEGO Dispers 670 TEGO Dispers 715 W

Addid 230 Addid 230


Antistatic additives Addid 240 Addid 240

Selection Tables_Architectural Coatings page 201


Waterborne Flexo- and Gravure Inks, (Overprint) Varnishes,
Defoaming

Waterborne formulations

Pigmented
Addition to the grinding stage Addition to the let-down stage Varnishes

TEGO Foamex 810 TEGO Foamex 843 TEGO Airex 902 W


TEGO Foamex 842 TEGO Foamex 845 TEGO Foamex 845
Styrene acrylic resin solutions and hybrids TEGO Foamex 831* TEGO Foamex 1488 TEGO Foamex 805 N

TEGO Foamex 810 TEGO Foamex 843 TEGO Foamex 842


TEGO Foamex 831* TEGO Foamex 845 TEGO Airex 902 W
Acrylic resin solutions and hybrids TEGO Foamex 842 TEGO Foamex 810 TEGO Foamex 805 N

TEGO Foamex 3062 TEGO Foamex 1488 TEGO Foamex 1488


TEGO Foamex 8050 TEGO Foamex 845 TEGO Foamex 822
Casein/maleics TEGO Foamex 831* TEGO Foamex 800 TEGO Foamex 815 N

TEGO Foamex 831* TEGO Foamex 843 TEGO Airex 902 W


TEGO Foamex 8050 TEGO Foamex 815 N TEGO Foamex 815 N
Acrylic/styrene-acrylic emulsions TEGO Airex 901 W TEGO Foamex 805 N TEGO Foamex 805 N

TEGO Foamex 842 TEGO Foamex 815 N TEGO Foamex 822


Polyurethane/polyurethane- TEGO Foamex 810 TEGO Foamex 800 TEGO Foamex 805 N
acrylic emulsions TEGO Foamex 830* TEGO Foamex 822 TEGO Airex 902 W

*
silicone-free

page 202 Selection Tables_Printing Inks


Printing Inks and Varnishes, Others

Others

Waterborne Solventfree Radiation-curing


formulations formulations formulations

TEGO Twin 4100 TEGO Glide 432


TEGO Wet KL 245 TEGO Wet 270 TEGO Rad 2010
Rewopol SB DO 75 TEGO Glide 410 TEGO Wet 270
Substrate wetting/craters TEGO Wet 510 TEGO Twin 4100 TEGO Rad 2200 N

TEGO Wet 510 TEGO Rad 2011


TEGO Flow 425 TEGO Flow 425
TEGO Glide 440 TEGO Glide A 115 TEGO Wet 500
Leveling TEGO Wet 270 TEGO Glide 440 TEGO Glide 432

TEGO Glide 482 TEGO Rad 2010


TEGO Glide 410 TEGO Glide 410 TEGO Glide 432
TEGO Glide 440 TEGO Glide 440 TEGO Rad 2250
Slip/scratch resistance, clear TEGO Glide 100 TEGO Glide A 115 TEGO Glide 435

TEGO Glide 482 TEGO Glide 410 TEGO Rad 2500


TEGO Glide 410 TEGO Glide 450 TEGO Glide 435
Slip/scratch resistance, pigmented TEGO Glide 450 TEGO Glide A 115 TEGO Rad 2010

TEGO Glide 482 TEGO Glide 410 TEGO Rad 2010


TEGO Glide 410 TEGO Glide 440 TEGO Rad 2500
Release effect/anti-blocking effect, clear TEGO Phobe 1401 TEGO Glide A 115 TEGO Rad 2700

TEGO Glide 482 TEGO Glide 410 TEGO Rad 2700


Release effect/anti-blocking effect, TEGO Phobe 1650 TEGO Glide 435 TEGO Rad 2500
pigmented TEGO Phobe 1401 TEGO Glide A 115 TEGO Rad 2010

TEGO Dispers 760 W


TEGO Dispers 765 W TEGO Dispers 710
Color strength development/settling TEGO Dispers 755 W TEGO Dispers 670 TEGO Dispers 656

TEGO Glide 482 TEGO Rad 2500


Hydrophobing/beading effect TEGO Phobe 1401 TEGO Phobe 1505 TEGO Rad 2700

TEGO Airex 931


TEGO Foamex N TEGO Airex 920
Defoaming, clear see separate table TEGO Airex 900 TEGO Airex 900

TEGO Airex 900


TEGO Airex 900 TEGO Foamex N
TEGO Foamex N TEGO Rad 2500
Defoaming, pigmented see separate table TEGO Airex 931 TEGO Airex 920

Selection Tables_Printing Inks page 203


Silk Screen Inks, Defoaming, Deaeration

Waterborne formulations, pigmented

Addition to the grinding stage Addition to the let-down stage Varnishes

TEGO Foamex 810 TEGO Airex 901 W TEGO Foamex 822


TEGO Foamex 8050 TEGO Foamex 845 TEGO Airex 902 W
Acrylics/styrene-acrylics TEGO Airex 901 W TEGO Foamex 822 TEGO Foamex 810

TEGO Foamex 810 TEGO Foamex 810 TEGO Foamex 822


TEGO Foamex 830* TEGO Foamex 822 TEGO Foamex 805 N
2-pack polyurethane, polyurethane TEGO Airex 901 W TEGO Foamex 800 TEGO Airex 902 W

TEGO Foamex 810 TEGO Foamex 822 TEGO Foamex 815 N


TEGO Foamex 840 TEGO Foamex 810 TEGO Airex 902 W
Alkyds/epoxies TEGO Foamex 831* TEGO Airex 902 W TEGO Foamex 810

*
silicone-free

Radiation-curing formulations

Varnishes Pigmented

TEGO Airex 900


TEGO Airex 920 TEGO Foamex N
TEGO Rad 2500 TEGO Airex 920

Solventborne formulations

Varnishes Pigmented

TEGO Glide B 1484 TEGO Airex 900


TEGO Flow ZFS 460 TEGO Foamex N
Epoxies TEGO Airex 900 TEGO Foamex 840

TEGO Foamex N
Polyurethanes TEGO Airex 931 TEGO Airex 962

Melamine-crosslinking acrylics, TEGO Airex 935 TEGO Airex 935


polyesters and alkyds TEGO Airex 931 TEGO Foamex N

TEGO Airex 931


TEGO Airex 931 TEGO Airex 935
Alkyds, acrylics, PVC TEGO Airex 935 TEGO Foamex N

page 204 Selection Tables_Printing Inks


Pigment Concentrates

Aqueous, binder-free

Transparent
Organic pigments Inorganic pigments Carbon blacks inorganic pigments

TEGO Dispers 755 W TEGO Dispers 755 W TEGO Dispers 755 W TEGO Dispers 752 W
Stabilization TEGO Dispers 741 W TEGO Dispers 653 TEGO Dispers 760 W TEGO Dispers 755 W

TEGO Dispers 760 W TEGO Dispers 660 C


Increase color strength TEGO Dispers 650 TEGO Dispers 741 W TEGO Dispers 760 W

TEGO Dispers 755 W TEGO Dispers 755 W TEGO Dispers 760 W


Reduce viscosity TEGO Dispers 741 W TEGO Dispers 653 TEGO Dispers 755 W

Improve colorant acceptance TEGO Dispers 660 C TEGO Dispers 660 C TEGO Dispers 660 C

Defoaming TEGO Foamex 810 TEGO Foamex 810 TEGO Foamex 810 TEGO Foamex 810

Reduce in-can drying-out TEGO Humectant 7000 TEGO Humectant 7000

Aqueous, binder-containing

Transparent
Organic pigments Inorganic pigments Carbon blacks inorganic pigments

TEGO Dispers 755 W TEGO Dispers 755 W TEGO Dispers 755 W


Stabilization TEGO Dispers 741 W TEGO Dispers 653 TEGO Dispers 760 W TEGO Dispers 755 W

TEGO Dispers 760 W TEGO Dispers 741 W TEGO Dispers 760 W


Increase color strength TEGO Dispers 650 TEGO Dispers 653 TEGO Dispers 650

TEGO Dispers 760 W TEGO Dispers 755 W TEGO Dispers 760 W


Reduce viscosity TEGO Dispers 741 W TEGO Dispers 653 TEGO Dispers 755 W

Improve colorant acceptance TEGO Dispers 660 C TEGO Dispers 660 C TEGO Dispers 660 C

Defoaming TEGO Foamex 810 TEGO Foamex 810 TEGO Foamex 810 TEGO Foamex 810

Selection Tables_Pigment Concentrates page 205


Solventborne

Transparent
Organic pigments Inorganic pigments Carbon blacks inorganic pigments

TEGO Dispers 670


Stabilization TEGO Dispers 670 TEGO Dispers 653 TEGO Dispers 710 TEGO Dispers 670

TEGO Dispers 670


Increase color strength TEGO Dispers 650 TEGO Dispers 656 TEGO Dispers 650

TEGO Dispers 670 TEGO Dispers 670


Reduce viscosity TEGO Dispers 656 TEGO Dispers 656 TEGO Dispers 670

Improve colorant acceptance TEGO Dispers 656 TEGO Dispers 656 TEGO Dispers 656

Reduce VOC TEGO VariPlus UC TEGO VariPlus UC TEGO VariPlus UC TEGO VariPlus UC

Universal pastes

Transparent
Organic pigments Inorganic pigments Carbon blacks inorganic pigments

TEGO Dispers 650 TEGO Dispers 653 TEGO Dispers 656


Stabilization TEGO Dispers 653 TEGO Dispers 653 TEGO Dispers 650 TEGO Dispers 653

Increase color strength TEGO Dispers 650 TEGO Dispers 660 C TEGO Dispers 650

TEGO Dispers 652


Reduce viscosity TEGO Dispers 656 TEGO Dispers 656 TEGO Dispers 653

TEGO Dispers 662 C TEGO Dispers 662 C TEGO Dispers 662 C TEGO Dispers 662 C
Improve colorant acceptance TEGO Dispers 656 TEGO Dispers 656 TEGO Dispers 656 TEGO Dispers 656

Defoaming TEGO Foamex 8050 TEGO Foamex 8050 TEGO Foamex 8050 TEGO Foamex 8050

Reduce in-can drying-out TEGO Humectant 7000 TEGO Humectant 7000

page 206 Selection Tables_Pigment Concentrates


Wood Coatings, Defoaming/Deaeration
by application method

Waterborne formulations

Curtain coatings

Addition to the grinding stage Addition to the let-down stage Clear

TEGO Foamex 810 TEGO Foamex 822 TEGO Airex 902 W


Acrylics TEGO Airex 902 W TEGO Foamex 800 TEGO Foamex 825

TEGO Foamex 822


TEGO Airex 902W TEGO Foamex 822 TEGO Foamex 800
Polyurethane acrylics/polyurethane TEGO Foamex 810 TEGO Foamex 805 N TEGO Airex 902 W

TEGO Airex 902 W TEGO Airex 902 W


2-pack polyurethane TEGO Foamex 800 TEGO Foamex 805 N TEGO Foamex 805 N

TEGO Airex 902 W


TEGO Airex 902 W TEGO Foamex 822
Alkyds, air-drying TEGO Foamex 822 TEGO Foamex 805 N TEGO Foamex 800

TEGO Airex 902 W TEGO Foamex 810


Acrylics/melamine TEGO Foamex 810 TEGO Foamex 825 TEGO Foamex 822

Spray, roller application, brushing

Addition to the grinding stage Addition to the let-down stage Clear

TEGO Airex 904 W TEGO Airex 902 W TEGO Foamex 810


TEGO Airex 901 W TEGO Foamex 845 TEGO Airex 904 W
Acrylics TEGO Foamex 810 TEGO Foamex 825 TEGO Foamex 825

TEGO Airex 902 W TEGO Foamex 822 TEGO Airex 902 W


TEGO Airex 904 W TEGO Foamex 800 TEGO Foamex 825
Polyurethane acrylics/polyurethane TEGO Foamex 810 TEGO Foamex 825 TEGO Foamex 822

TEGO Airex 902 W


TEGO Airex 902 W TEGO Foamex 805 N TEGO Foamex 822
2-pack polyurethane TEGO Foamex 822 TEGO Foamex 800 TEGO Foamex 800

TEGO Airex 902 W TEGO Airex 902 W


TEGO Airex 904 W TEGO Foamex 822 TEGO Foamex 822
Alkyds, air-drying TEGO Foamex 810 TEGO Foamex 805 N TEGO Foamex 810

TEGO Airex 902 W TEGO Foamex 810


TEGO Foamex 810 TEGO Foamex 825 TEGO Airex 902 W
Acrylics/melamine TEGO Airex 904 W TEGO Foamex 800 TEGO Foamex 825

Selection Tables_Wood Coatings page 207


Airless application

Addition to the grinding stage Addition to the let-down stage Clear

TEGO Foamex 845 TEGO Airex 902 W


TEGO Airex 901 W TEGO Foamex 825 TEGO AIrex 904 W
Acrylics TEGO Airex 904 W TEGO Foamex 823 TEGO Airex 901 W

TEGO Airex 902 W


TEGO Airex 902 W TEGO Foamex 822 TEGO Foamex 810
Polyurethane acrylics/polyurethane TEGO Airex 901 W TEGO Foamex 800 TEGO Foamex 825

TEGO Foamex 800 TEGO Airex 902 W


2-pack polyurethane TEGO Airex 902 W TEGO Foamex 822 TEGO Foamex 825

TEGO Airex 902 W TEGO Foamex 800 TEGO Airex 902 W


Alkyds, air-drying TEGO Airex 904 W TEGO Foamex 822 TEGO Foamex 810

TEGO Airex 901 W TEGO Foamex 825 TEGO Airex 902 W


Acrylics/melamine TEGO Airex 904 W TEGO Foamex 845 TEGO Airex 904 W

Solventborne/radiation-curing formulations

Spray, roller application, brushing etc Curtain coating

TEGO Airex 931 TEGO Airex 962


TEGO Airex 936 Polyurethane TEGO Airex 990
Polyurethane TEGO Airex 990
Cellulose nitrate/Cellulose nitrate combinations TEGO Airex 936
TEGO Airex 936
Cellulose nitrate/Cellulose nitrate combinations TEGO Airex 931 Alkyds, air-drying TEGO Airex 962

TEGO Airex 936 Acid-curing TEGO Airex 936


TEGO Airex 931 TEGO Airex 910
Alkyds, air-drying TEGO Airex 940 Unsaturated polyesters TEGO Airex 962
TEGO Airex 936 TEGO Airex 920
Acrylics/melamine TEGO Airex 931 Radiation-curing TEGO Airex 910
TEGO Airex 940
TEGO Airex 910
Unsaturated polyesters TEGO Airex 990

TEGO Airex 920


TEGO Airex 900
Radiation-curing TEGO Airex 962

page 208 Selection Tables_Wood Coatings


Wood Coatings, Others
Waterborne formulations

TEGO Wet 270


TEGO Twin 4100
TEGO Wet 280
Substrate wetting/anti-crater TEGO Glide 110*

TEGO Glide 410*


Slip/scratch resistance TEGO Glide 482*

TEGO Glide 410*


Anti-blocking TEGO Glide 482*

TEGO Wet 250


TEGO Twin 4100
TEGO Flow 425
TEGO Glide 100
Leveling/orange peel effect TEGO Wet 500

TEGO Dispers 755 W


TEGO Dispers 752 W
Floating/rub-up TEGO Dispers 650
Floating/settling TEGO Dispers 653

TEGO Phobe 1401


Hydrophobing TEGO Phobe 1500 N

*
only top coat

Radiation-curing (non waterborne) formulations

TEGO Glide 432*


TEGO Wet 270
TEGO Rad 2250*
Substrate wetting/anti-crater TEGO Wet 280

TEGO Glide 440*


TEGO Rad 2250*
Glossy formulations Slip/scratch resistance/anti-blocking/air-draught sensitivity TEGO Rad 2200 N*

TEGO Glide 432*


TEGO Rad 2500*
TEGO Glide 410*
Matte formulations Slip/scratch resistance/anti-blocking/air-draught sensitivity TEGO Rad 2300*

TEGO Flow 370


TEGO Flow 425
TEGO Glide 100
Leveling/orange peel effect TEGO Rad 2011

TEGO Dispers 610 S


Floating/rub-up TEGO Dispers 656
Floating/settling TEGO Dispers 670

Wetting matting agent TEGO Dispers 688

*
only top coat

Selection Tables_Wood Coatings page 209


Solventborne formulations

TEGO Glide 410*


TEGO Glide 110*
Substrate wetting/anti-crater TEGO Glide 406

TEGO Glide 410


Glossy formulations Slip/scratch resistance/air-draught sensitivity TEGO Glide 450

Slip/scratch resistance/air-draught sensitivity/ TEGO Glide 410


Matte formulations orientation of matting agents TEGO Glide A 115

TEGO Glide 410


Anti-blocking TEGO Glide A 115

TEGO Glide 100


TEGO Flow 370
Leveling/orange peel effect TEGO Flow 425

TEGO Glide 410*


TEGO Glide 406
Floating/Bnard-cells TEGO Dispers 610 S

TEGO Dispers 670


TEGO Dispers 656
TEGO Dispers 700
Floating/rub-up TEGO Dispers 710

TEGO Dispers 630


Sagging/settling TEGO Dispers 610

*
only top coat

page 210 Selection Tables_Wood Coatings


Industrial Coatings, Defoamer/Deaerator

Waterborne formulations

Addition to the grinding stage Addition to the let-down stage

TEGO Foamex 810 TEGO Foamex 825


TEGO Foamex 830 TEGO Foamex 822
Acrylics/PU-acrylics TEGO Airex 901 W TEGO Airex 902 W

TEGO Foamex 810 TEGO Airex 902 W


TEGO Foamex 830 TEGO Foamex 822
2-pack polyurethane/polyurethane TEGO Airex 901 W TEGO Foamex 805 N

TEGO Foamex 810 TEGO Foamex 815 N


TEGO Foamex 840 TEGO Foamex 822
Epoxies TEGO Foamex 883 TEGO Foamex 8030

TEGO Foamex 8050 TEGO Foamex 843


TEGO Foamex 810 TEGO Foamex 1488
Styrene acrylics TEGO Airex 901 W TEGO Foamex 902

TEGO Airex 901 W TEGO Foamex 822


TEGO Foamex 810 TEGO Foamex 805 N
Stoving systems TEGO Wet 505 TEGO Foamex 843

TEGO Foamex 810 TEGO Foamex 822


TEGO Foamex 830 TEGO Foamex 805 N
Alkyds TEGO Wet 505 TEGO Foamex 815 N

Solventborne systems

Primer Top coat

TEGO Glide B 1484 TEGO Airex 900


TEGO Flow ZFS 460 TEGO Glide B 1484
Epoxies TEGO Airex 944 TEGO Airex 944

TEGO Airex 944 TEGO Airex 990


TEGO Airex 990 TEGO Airex 931
Polyurethane TEGO Airex 991 TEGO Airex 945

TEGO Airex 962


Melamine-crosslinking acrylics, TEGO Airex 931 TEGO Airex 931
polyesters and alkyds TEGO Airex 990 TEGO Airex 990

TEGO Airex 931 TEGO Airex 931


TEGO Airex 944 TEGO Flow 370
Alkyds, polyesters, PVC TEGO Airex 990 TEGO Airex 990

TEGO Airex 931 TEGO Airex 931


TEGO Flow 370 TEGO Airex 990
Thermoplastic acrylics TEGO Airex 990 TEGO Flow 370

TEGO Airex 931


Cellulose nitrate TEGO Airex 931 TEGO Airex 962

Selection Tables_Industrial Coatings page 211


Industrial Coatings, Others

Waterborne formulations

Electrodeposition Primer Top coat

TEGO Wet 270 TEGO Wet 270


Substrate wetting/craters/ TEGO Wet 500 TEGO Twin 4100 TEGO Twin 4100
contaminated substrates TEGO Wet 270 TEGO Wet 280 TEGO Wet 280

TEGO Glide 482


TEGO Glide 100 TEGO Glide 410
Slip/scratch resistance n.a. TEGO Glide 450 TEGO Glide 450

TEGO Wet 270 TEGO Wet 270


TEGO Wet 500 TEGO Twin 4100 TEGO Twin 4100
Leveling/orange peel effect TEGO Wet 505 TEGO Flow 425 TEGO Flow 425

TEGO Dispers 750 W TEGO Dispers 651 TEGO Dispers 755 W


TEGO Dispers 651 TEGO Dispers 750 W TEGO Dispers 741 W
Floating/rub-up/settling TEGO Dispers 741 W TEGO Dispers 741 W TEGO Dispers 650

TEGO Dispers 650 TEGO Dispers 651 TEGO Dispers 755 W


Color strength development/ TEGO Dispers 750 W TEGO Dispers 750 W TEGO Dispers 741 W
color stability TEGO Dispers 741 TEGO Dispers 741 W TEGO Dispers 650

Solventborne systems

Primer Top coat

TEGO Wet 270 TEGO Wet 270


Substrate wetting/craters/ TEGO Wet KL 245 TEGO Glide 410
contaminated substrates TEGO Glide 415 TEGO Glide 450

TEGO Glide 410


TEGO Glide 415 TEGO Glide 450
Slip/scratch resistance TEGO Glide 450 TEGO Glide 415

TEGO Flow 425 TEGO Flow 425


TEGO Glide 100 TEGO Glide 100
Leveling/orange peel effect TEGO Flow 300 TEGO Flow 370

TEGO Dispers 610 S TEGO Dispers 710


TEGO Glide B 1484 TEGO Glide 415
Floating/Bnard cells TEGO Dispers 630 TEGO Glide 100

TEGO Dispers 670 TEGO Dispers 670


Floating/rub-up TEGO Dispers 656 TEGO Dispers 710

TEGO Dispers 630


TEGO Dispers 630 TEGO Dispers 610
Sagging/settling TEGO Dispers 610 TEGO Dispers 650

Color strength development/ TEGO Dispers 670 TEGO Dispers 670


color stability TEGO Dispers 656 TEGO Dispers 710

page 212 Selection Tables_Industrial Coatings


Leather Coatings

Leather coatings

Waterborne Solventborne
formulations formulations

TEGO Airex 901 W


TEGO Foamex 825
TEGO Foamex 822
Defoaming/deaeration varnish TEGO Foamex 800 TEGO Flow ZFS 460

TEGO Airex 901 W


Defoaming/deaeration, TEGO Foamex 810
addition to the grinding stage TEGO Foamex 8050 TEGO Airex 900

TEGO Foamex 825


Defoaming/deaeration, TEGO Foamex 822
addition to the let-down stage TEGO Foamex 800 TEGO Flow ZFS 460

TEGO Wet 250


TEGO Wet KL 245 TEGO Glide 410
Substrate wetting/craters TEGO Wet 265 TEGO Wet 270

TEGO Glide 410


TEGO Glide 440 TEGO Glide ZG 400
Leveling TEGO Glide 450 TEGO Glide 410

TEGO Glide L 404


TEGO Glide L 401 TEGO Glide 410
TEGO Glide 410 TEGO Glide ZG 400
Touch and handle modification TEGO Glide 482 TEGO Glide 450

TEGO Glide 482 TEGO Glide 410


Anti-blocking effect TEGO Glide 410 TEGO Glide 100

Water resistance/beading-effect TEGO Phobe 1401 TEGO Phobe 1500 N

TEGO Dispers 750 W


TEGO Dispers 760 W
Color strength development/ TEGO Dispers 752 W TEGO Dispers 710
hiding power TEGO Dispers 755 W TEGO Dispers 670

TEGO Dispers 610


TEGO Dispers 735 W TEGO Dispers 670
Pigment settling TEGO Dispers 760 W TEGO Dispers 710

Binder/Co-Binder Silikopur 8080

Selection Tables_Leather Coatings page 213


Silicone Resins, High Temperature Resistant Coatings
Applications from 250C up to 600C depending on the binder and the formulation

Ovens, chimneys, Exhaust pipes, Electric and


oven inserts mufflers gas heaters Barbecue grills

SILIKOPHEN P 40/W **

SILIKOPHEN P 50/X

SILIKOPHEN P 80/X

SILIKOFTAL HTF

SILIKOFTAL HTL

SILIKOFTAL HTL 2

SILIKOFTAL HTL 3

SILIKOFTAL HTS

SILIKOFTAL HTT

SILIKOPON EW

SILIKOPON EC

SILIKOFTAL non-stick 60

Applications up to 250C depending on the binder and the formulation

Toaster,
electric Slide coatings,
Bakeware Bakeware household Iron soles, Cookware, Barbecue garden shears,
exterior interior appliances waffle irons egg cookers grills screws

SILIKOFTAL HTF

SILIKOFTAL HTL

SILIKOFTAL HTL 2

SILIKOFTAL HTL 3

SILIKOFTAL HTS

SILIKOFTAL HTT

SILIKOPON EW

SILIKOPON EC

SILIKOFTAL non-stick 60

recommended well recommended especially recommended depending on the formulation


*
water-thinnable
**

page 214 Selection Tables_Silicone Resins


Silicone Resins, Industrial Coatings
High Solids 2-pack isocyanate-free

Maintenance
Metal/concrete Coil Coating Marine Coating General Industry Anti-Graffiti

SILIKOPON EF

SILIKOFTAL ED

Waterborne silicone modified polyurethane emulsion

Leather Coatings Wood Coatings Textile Coatings Plastic Coatings

SILIKOPUR 8080**

recommended well recommended especially recommended **


water-thinnable

Co-Binders
Application areas TEGO AddBond

LTW/
HS LTH LTW-B 2220 ND 2325 1270 DS 1300

Can Coating + + + o

Coil Coating + + + o

Automobil OEM coatings + o + +

Container paints + o + o + o

Floor coatings +

Metal paints + + + + + + +

Paints for packaging + + + + o +

Paints for plastics + + + + + + +

Anti-corrosion coatings + + + + + +

Primer (air-drying) + o +

Primer (stoving) + o + + o o +

Printing Inks +

Roadmarking paints + + + + +

Waterborne coatings + +

Adhesives + + + o o +

Hot stamping foils + +

UV curing coatings +

+ recommended application o possible application limited application

Selection Tables_Silicone Resins_Co-Binders page 215


Application areas TEGO VariPlus

UC/ UC
AP SK 1201 TF CA TC DS 50 W 40 3350 UV

Wood coatings + + + o +

Plastic coatings o + + + + + + (UV)

Anti-corrosion paints + + + o o

Paints for concrete + + o

Roadmarking paints + + + o

Industrial coatings + + + o + o

Lacquer for papers + + + +

Ball point pen pastes + o +

Adhesives + o + + o o (UV)

Pigment preparations o o + o + + +

Printing inks + + + + + (UV)

Hot stamping foils + + +

UV curing coatings + + o o o o +

+ recommended application o possible application limited application

Silica-Nanocomposites
Application areas Nanocryl

Plastics Plastics Textile/ Paper/


Substrates Wood (rigid) (flexible) Metal Glass Leather Cardboard

Automotive

Furniture

Construction

Wood flooring

Industrial coatings (non-automotive)

CD/DVD

Optical/Lenses

Coil

Consumer goods

Print/Packaging

Miscellaneous

page 216 Selection Tables_Co-Binders_Silica-Nanocomposites


Application areas Nanopol

Plastics Plastics Textile/ Paper/


Substrates Wood (rigid) (flexible) Metal Glass Leather Cardboard

Automotive

Furniture

Construction

Wood flooring

Industrial coatings (non-automotive)

Optical/Lenses

Coil

Consumer goods

Print/Packaging

Electronics, wire

Miscellaneous

Application areas Nanopox

Plastics Plastics Textile/


Substrates Wood (rigid) (flexible) Metal Leather

Automotive

Furniture

Construction

Wood flooring

Industrial coatings (non-automotive)

Coil

Consumer goods

Print/Packaging

Electronics, wire

Miscellaneous

Selection Tables_Silica-Nanocomposites page 217


page 218 The Big Tego_Technical Data Sheets
Technical Data Sheets
Please click here, to access the most current technical data sheets.

The Big Tego_Technical Data Sheets page 219


Trademarks
Some of the products mentioned in this brochure are registered trademarks
of third companies.

The holders of the trademarks at the time of publication of The Big TEGO
can be found in the list below:

Holders of the trademarks

Mentioned trademarks Registered trademark of

ACRONAL BASF SE

ACTICIDE Thor GmbH

AICA AICA Kogyo Co

AMP-90 The Dow Chemical Company or an affiliated company of Dow

BENTONE Elementis Specialties Inc.

BETOLIN Wllner GmbH & Co. KG

BLANC FIXE Sachtleben Chemie GmbH

CALCIMATT OMYA AG

CALGON Reckitt Benckiser N.V.

COL.9 BASF SE

COLLACRAL BASF SE

DESAVIN Bayer AG

DOWANOL The Dow Chemical Company or an affiliated company of Dow

HEUCODUR Dr. Hans Heubach GmbH & Co. KG

HEUCOPHOS Dr. Hans Heubach GmbH & Co. KG

KRONOS Kronos Titan GmbH

NATROSOL Hercules Incorporated

OMYACARB Omya AG

PLASTORIT Imerys Talc Austria GmbH

SIBELITE SCR Sibelco Naamloze Vennootschap

SIKRON Quarzwerke GmbH

SOCAL Solvay (Socit Anonyme)

STAPA Eckart GmbH

SURFYNOL AIR PRODUCTS AND CHEMICALS INC.

TYLOSE SE Tylose GmbH & Co. KG

WALOCEL Dow Wolff Cellulosics GmbH

page 220 Trademarks


Copy & Fax Order Form  Sales Support Fax: +49 201 173-1939
name postal code/city

company phone

street fax

country e-mail

I would like to receive:


Please mark as indicated and state the desired product number.

Product information & samples


data sheet sample product group product name product number

Defoamers TEGO Foamex

Deaerators TEGO Airex

TEGO Glide

Glide and Flow Additives TEGO Flow

Radiation-Curing Additives TEGO Rad

TEGO Wet

Substrate Wetting Additives TEGO Twin

Wetting and Dispersing Additives TEGO Dispers

Hydrophobing Agents TEGO Phobe

Rheological Additives TEGO ViscoPlus

Anti-Graffiti Resins TEGO Protect

TEGO AddBond

Co-Binders TEGO VariPlus

SILIKOPHEN

SILIKOFTAL

SILIKOPON

Specialty Binders SILIKOPUR

NANOCRYL

NANOPOL

Silica-Nanocomposites NANOPOX

Others

General information Brochures for application field (if available)

Product Overview Architectural Coatings


The Big TEGO Printing Inks and Varnishes
The Little Tego High Solids

Guiding formulations Plastic Coatings


for manufacturing silicone paints for heat resistance TEGO AddBond
or pigment concentrates
Publications regarding the following subjects: TEGO VariPlus

For your order please choose a language


English
German

Further information you can find under www.tego.de


TEGO Hotline +49 201 173-2222
This information and all further technical advice are
based on our present knowledge and experience.
However, it implies no liability or other legal respon-
sibility on our part, including with regard to existing
third party intellectual property rights, especially
patent rights. In particular, no warranty, whether ex-
press or implied, or guarantee of product properties
in the legal sense is intended or implied. We reserve
the right to make any changes according to techno-
logical progress or further developments. The cus-
tomer is not released from the obligation to conduct
careful inspection and testing of incoming goods.
Performance of the product described herein should
be verified by testing, which should be carried out
only by qualified experts in the sole responsibility of
a customer. Reference to trade names used by other
companies is neither a recommendation, nor does it
imply that similar products could not be used.

Evonik Industries AG
Goldschmidtstrae 100
45127 Essen
Germany
phone +49 201 173-2222
fax +49 201 173-1939
www.tego.de
www.evonik.com

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