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Understanding some of the basic properties of the polymers used in coatings is essen‐
tial for the formulator while developing a high-performance product. Many of the basic
properties of polymers are predictable based on their structural features i.e. linear,
branched, rigid, or flexible.
One such property of resins that holds key importance is “Glass Transition
Temperature”. Each coating’s glass transition temperature (Tg) is a net result of the ef‐
fects of its constituents as well as the composition and ratio of the resin used.
For any coating chemist, the glass transition temperature is an important thermal prop‐
erty of coatings which contributes to determining their application area and service life
properties.
Let's review the basics of glass transition temperature and the factors that govern it.
Glass Transition Temperature, Tg, is defined as a temperature at which resin changes from a rigid glassy
material to a soft material. It is not a melting point but involves the material becoming “softer”. This tem‐
perature (measured in °C or °F) depends on the chemical structure of the resin and can therefore be used
to select the right resin depending upon the end-use of coatings.
Physically, the glass transition temperature is the point at which polymer chains gain enough energy to
increase their mobility within the polymer matrix. The transition from the glass to the rubber-like state is
an important feature of polymer behavior, marking a region of dramatic changes in the physical proper‐
ties, such as hardness and elasticity of the coating.
The Tg is a very intricate concept and is not represented by a single value, even though it is an excellent
starting point for understanding coating dynamics.
The glass transition temperature of a polymer can be understood in terms of the Free Volume Theory.
The free volume is a measure of the internal space available within a polymer matrix. When the free vol‐
ume increases, so do the freedom of movement of polymer chains.
A polymer chain that can move around easily will have an extremely low Tg, while one that doesn't
move so well will have a high one.
A polymer at Tg or below its Tg has no free volume for the polymer chains to move. Heating a poly‐
mer above its Tg increases the free volume and makes the mobility of the polymer chains possible.
The free volume theory states that a consistent value of 2.5% free volume is required to achieve segmen‐
tal motion.
Free Volume Theory: Volume Changes in Polymers as Temperature Increases
(Source: Research Gate)
There are several factors that govern the glass transition temperature of coating. It is imperative to be
aware of these factors to find out how coatings perform in a given service conditions and how Tg can
vary with changes in formulation, application, cure and crosslinking, and environmental parameters.
The most common factors that determines Tg of coating is the resin use. Resins are broadly classified
into three groups – thermoplastics, thermosets, and elastomers. They can be further divided into two
types according to their molecular arrangements i.e. amorphous and crystalline.
Amorphous polymers have a random molecular structure that does not have a sharp melting point.
Instead, amorphous material softens gradually as temperature rises. Amorphous polymers only ex‐
hibit a Tg.
Crystalline or Semi-crystalline polymers have a highly ordered molecular structure. These do not
soften as the temperature rises but have a defined and narrow melting point. Crystalline polymers
exhibit a Tm (melt temperature) and typically a Tg since there is usually an amorphous portion as
well (“semi”-crystalline).
A Heat Versus Temperature Plot for a Crystalline Polymer (L) and Amorphous Polymer (R)
A Heat Versus Temperature Plot for a Crystalline Polymer (L) and Amorphous Polymer (R)
(Source: PSLC)
KEY FACTS
Typical thermoset polymer will exhibit high Tg due to restricted molecular mobility driven by higher den‐
sity and higher quantity of crosslinks (e.g. multifunctional epoxies). While thermoplastic polymer chains
are capable of a wider range of movement in terms of flow or translational motion. But thermoplastics
with rigid backbone structures tend to have higher Tg because of:
Bulky side groups that restrict/hinder rotation around the primary chain, and
Intermolecular interactions
For example, linear aliphatic amorphous polymers are more likely to have low Tg (such as high-density
polyethylene, Tg = -120 to -130°C), in contrast to polymers with more rigid backbone structures, e.g.,
poly(benzimidazole), with a Tg of ~ 490-500°C.
The chemical building blocks of a polymer, i.e., backbone, side chains, and chain-to-chain interactions,
and how all the chemistry is connected plays a distinctively significant role in finding the glass transition
temperature.
Other factors that have a significant impact on glass transition temperature are:
Branching
Alkyl chain length
Bond interaction
Flexibility of polymer chain
Film thickness, etc.
When focused on coatings, we also need to consider the polymer’s interactions with pigments, additives,
plasticizers, residual solvents, the substrate, and the influence of environmental conditions.
Pigments and extenders are important Pigments for Paints, Coatings and Inks
constituents of coatings and their physical properties play a key role in defining the final properties of
coatings. Pigment Volume Concentration, PVC, indicates the volumetric concentration of extenders (or
pigments) in the coating.
CPVC (Critical Pigment Volume Concentration) stands for PVC corresponding to the random tightest
possible packing of the extender (or pigment) particles and the minimum amount of binder necessary to
fill the interstices between extender particles. Pigment volume concentration (PVC) influences mechani‐
cal behavior of the coatings, thus influences glass transition temperature of coatings.
Addition of Plasticizers
Addition of plasticizer increases the free volume in polymer structure. Plasticizers not only increase elas‐
ticity but also lower the glass transition temperature, which adversely affects blocking stability and can
lead to sticky surfaces.
This results in polymer chains sliding past each other more easily. As a result, the polymer chains can
move around at lower temperatures resulting in decrease in Tg of a polymer.
» Get Tips to Select the Right Plasticizer for Your Coatings Application!
Coalescing Agents
Coalescing agents function as temporary plasticizers for the polymer particle and thereby reduce the
minimum film forming temperature* (MFFT). The MFFT of the emulsion relates directly to the glass-tran‐
sition temperature (Tg) of the polymer.
Coalescing agents allow the formation of polymeric films at ambient temperature conditions of film ap‐
plication, even of polymers showing a MFFT of above these temperature conditions. Coalescing agents
typically lowers Tg of the polymer.
*The minimum film-forming temperature is the lowest temperature required to coalesce a polymer and ap‐
plied to a substrate into a thin film.
Increase in moisture content leads formation of hydrogen bonds with polymeric chains increasing the
distance between polymeric chains. And, hence increases the free volume and decreases Tg.
The value of entropy for amorphous material is higher and low for crystalline material. If value of entropy
is high, then value of Tg is also high.
Increase in pressure of surrounding leads to decrease in free volume and ultimately high Tg. Overall, it is
the resin’s structure, molecular weight, crosslinking, functional groups, interaction with other components
of the formulation and application conditions, all have direct impact on glass transition temperature.
It is also important to note that Tg is an important property while studying viscosity at a given tempera‐
ture, physical and chemical properties of the coating formulation.
Glass Transition Temperature for Specific Applications
Now we are aware that understanding the glass transition temperature can be critical for determining
coating suitability for specific applications. Tg is an especially important consideration in the selection
of the proper resin for a for desired coating performance.
Here are the few examples (not an exhaustive list yet) explaining:
Compared to conventional coatings, the UV vari‐ The corrosion coating must have a glass transi‐
ants are comprised of lower molecular weight tion temperature, Tg, above the operating temper‐
materials that react to make denser, highly cross- ature of the pipeline to prevent damage from pipe
linked networks. They also often have higher Tg movement.
and make harder films with good abrasion and
chemical resistance.
Multifunctional epoxy resins have commonly been Industrial paints and coatings need a higher Tg
used to produce highly crosslinked coatings with because high hardness and the lack of tack are
high glass transition temperatures. The Tg of an requirements at the service temperatures, mean‐
epoxy is affected not only by the choice of epoxy, ing the coating will be more rigid and less sus‐
curing agent and filler used, but also by the curing ceptible to dirt pick-up.
conditions. Epoxies demonstrate a wide range of
Tg, from as low as 50°C to upwards of 250°C. In
addition to improving its performance properties,
adding heat while curing the epoxy helps improve
its glass transition temperature (Tg).
Several methods are available to measure glass transition temperature that typically provide a range of
values with subtle to significant differences. These test methods include:
Among these methods, DSC, DTA and DMA are by far the most dominant techniques used for glass tran‐
sition temperature measurements.
Differential Scanning Calorimetry (DSC) is a thermo-analytical technique used to study the thermal prop‐
erties of the polymer using a differential scanning calorimeter. It is widely used to determine the glass
transition temperatures of resins. This test method applies to amorphous materials or to partially crys‐
talline materials containing amorphous regions, that are stable and do not undergo decomposition or
sublimation in the glass transition region.
In this method, a differential scanning calorimeter measures the difference in heat flow to a sample and
to a reference against time or temperature while the temperature change of the sample, in a specified at‐
mosphere, is programmed.
Glass Transition Temp. Measurements of Different Polymers Using DSC
Glass Transition Temp. Measurements of Different Polymers Using DSC
(Source: Mettler-Toledo Analytical)
The test standards used to find Glass Transition Temperature of resins via DSC include:
ASTM E1356-08 (2014) – Standard Test Method for Assignment of the Glass Transition
Temperatures by Differential Scanning Calorimetry
ISO 16805:2003 – Binders for paints and varnishes — Determination of glass transition
temperature
ASTM D3418-15 – Standard Test Method for Transition Temperatures and Enthalpies of Fusion and
Crystallization of Polymers by Differential Scanning Calorimetry
ASTM D6604-00(2017) – Standard Practice for Glass Transition Temperatures of Hydrocarbon
Resins by Differential Scanning Calorimetry
ISO 11357-1:2016 – Plastics — Differential scanning calorimetry (DSC)
Part 1: General principles
Part 2: Determination of glass transition temperature and step height
Differential Thermal Analysis (DTA) is a popular thermal analysis technique and is often employed for
measuring Tg of the material. In principle, differential thermal analysis is a technique which is similar to
differential scanning calorimetry (DSC).
The test standards used to determine Glass Transition Temperature of resins via DTA include:
ASTM E794 - 06(2018) – Standard Test Method for Melting and Crystallization Temperatures by
Thermal Analysis
Dynamic Mechanical Analyzer measures the stiffness of materials as a function of temperature, humid‐
ity, dissolution media or frequency.
In this technique, a mechanical stress is applied to the sample and the resultant strain is measured by
the instrument. These parameters are used to evaluate glass transitions, degree of crystallinity and stiff‐
ness behavior of the sample.
When dealing with films and coatings, DMA is applied in 3 different options:
Application of DMA
Application of DMA
The test standards used to determine Glass Transition Temperature of resins via DMA include:
ASTM E1640 - 13 – Standard Test Method for Assignment of the Glass Transition Temperature by
Dynamic Mechanical Analysis
Note: It is imperative to understand when, how, and why coatings perform as they do from varying applica‐
tion methods, differing cure profiles, and a wide array of environmental conditions.
Get Inspired: DMA Practical Interpretation with Case studies for Polymer Development
Good
Great article for those of us who barely knows about Tg & MFFT although we would like
to learn more about DSC technics and how modifications on coatings formulation could
affect directly to Tg properties
Very nice article for those of us who are just learning about coating formulation and fail‐
ure analysis.
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