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Polysulfone

Introduction:

Polysulfones are a family of high performance thermoplastics. These polymers are known for their toughness and stability at
high temperatures. Technically used polysulfones contain an aryl-SO2-aryl subunit. Due to the high cost of raw materials and
processing, polysulfones are used in specialty applications and often are a superior replacement for polycarbonates.

Three polysulfones are used industrially, these are polysulfone (PSU), polyethersulfone (PES) and polyphenylene sulfone (PPSU).
They can be used in the temperature range from -100 to +200 °C and are used for electrical equipment, in vehicle construction
and medical technology.[1] They are composed of para-linked aromatics, sulfonyl groups and ether groups and partly also alkyl
groups. Polysulfones have outstanding resistance to heat and oxidation, hydrolysis resistance to aqueous and alkaline media
and good electrical properties.[2]

Nomenclature

The term "polysulfone" is normally used for polyarylethersulfones (PAES), since only aromatic polysulfones are used
commercially. Furthermore, since ether groups are always present in these polysulfones, PAESs are also referred to as
polyether sulfones (PES), poly(arylene sulfone)s or simply polysulfone (PSU).

Production

Historical

The simplest polysulfone poly(phenylene sulfone), known as early as 1960, is produced in a Friedel-Crafts reaction from
benzenesulfonyl chloride:[3]

n C6H5SO2Cl → (C6H4SO2)n + n HCl

With a melting point over 500 °C, the product is difficult to process. It exhibits attractive heat resistance, but its mechanical
properties are rather poor. Polyarylether sulphones (PAES) represent a suitable alternative. Appropriate synthetic routes to
PAES were developed almost simultaneously, and yet independently, from 3M Corporation,[4] Union Carbide Corporation in
the United States,[5] and ICI's Plastics Division[6] in the United Kingdom. The polymers found at that time are still used today,
but produced by a different synthesis process.

The original synthesis of PAES involved electrophilic aromatic substitution of an diaryl ether with the bis (sulfonyl chloride) of
benzene. Reactions typically use a Friedel-Crafts catalyst, such as ferric chloride or antimony pentachloride:

n O(C6H5)2 + n SO2Cl2 → ,*O(C6H4)2+SO2-n + 2n HCl

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This route is complicated by the formation of isomers arising from both para- and ortho- substitution. Furthermore, cross-
linking was observed, which strongly affects the mechanical properties of the polymer.[7][4] This method has been abandoned.

Contemporary production methods

PAES are currently prepared by a polycondensation reaction of diphenoxide and bis(4-chlorophenyl)sulfone (DCDPS). The
sulfone group activates the chloride groups toward substitution. The required diphenoxide is produced in situ from a diphenol
and sodium hydroxide. The cogenerated water is removed by azeotropic distillation using toluene or chlorobenzene). The
polymerization is carried out at 130–160 °C under inert conditions in a polar, aprotic solvent, e.g. dimethyl sulfoxide, forming a
polyether concomitant with elimination of sodium chloride:

Bis(4-fluorophenyl)sulfone can be used in place of bis(4-chlorophenyl)sulfone. The difluoride is more reactive than the
dichloride but more expensive. Through chain terminators (e.g. methyl chloride), the chain length can be controlled for melt-
processing.

The diphenol is typically bisphenol-A or 1,4-dihydroxybenzene. Such step polymerizations require highly pure monomer and
precise stoichiometry to ensure high molecular weight products.[8]

DCDPS is the precursor to polymers known as Udel (from bisphenol A), PES, and Radel R. Udel is a high-performance
amorphous sulfone polymer that can molded into a variety of different shapes. It is both rigid and temperature-resistant, and
has applications in everything from plumbing pipes, to printer cartridges, to automobile fuses. DCDPS also reacts with bisphenol
S to form PES. Like Udel, PES is a rigid and thermally-resistant material with numerous applications.

Properties

Polysulfones are rigid, high-strength and transparent. They are also characterized by high strength and stiffness, retaining these
properties between −100 °C and 150 °C. The glass transition temperature of polysulfones is between 190 and 230 °C.[9] They
have a high dimensional stability, the size change when exposed to boiling water or 150 °C air or steam generally falls below
0.1%.[10] Polysulfone is highly resistant to mineral acids, alkali, and electrolytes, in pH ranging from 2 to 13. It is resistant to
oxidizing agents (although PES will degrade over time[11]), therefore it can be cleaned by bleaches. It is also resistant to
surfactants and hydrocarbon oils. It is not resistant to low-polar organic solvents (e.g. ketones and chlorinated hydrocarbons)
and aromatic hydrocarbons. Mechanically, polysulfone has high compaction resistance, recommending its use under high
pressures. It is also stable in aqueous acids and bases and many non-polar solvents; however, it is soluble in dichloromethane
and methylpyrrolidone.[8] Polysulfones are counted among the high performance plastics. They can be processed by injection
molding, extrusion or hot forming.

Structure-property relationship
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Poly(aryl ether sulfone)s are composed of aromatic groups, ether groups and sulfonyl groups. For a comparison of the
properties of individual constituents poly(phenylene sulfone) can serve as an example, which consists of sulfonyl and phenyl
groups only. Since both groups are thermally very stable, poly(phenylene sulfone) has an extremely high melting temperature
(520 °C). However, the polymer chains are also so rigid that poly(phenylene sulfone) (PAS) decomposes before melting and can
thus not be thermoplastically processed. Therefore, flexible elements must be incorporated into the chains, this is done in the
form of ether groups. Ether groups allow a free rotation of the polymer chains. This leads to a significantly reduced melting
point and also improves the mechanical properties by an increased impact strength.[7] The alkyl groups in bisphenol A act also
as a flexible element.

The stability of the polymer can also be attributed to individual structural elements: The sulfonyl group (in which sulfur is in the
highest possible oxidation state) attracts electrons from neighboring benzene rings, causing electron deficiency. The polymer
therefore opposes further electron loss, thus substantiating the high oxidation resistance. The sulfonyl group is also linked to
the aromatic system by mesomerism and the bond therefore strengthened by mesomeric energy. As a result, larger amounts of
energy from heat or radiation can be absorbed by the molecular structure without causing any reactions (decomposition). The
result of the mesomerism is that the configuration is particularly rigid. Based on the biphenylsulfonyl group, the polymer is thus
durable heat resistant, oxidation resistant and still has a high stiffness even at elevated temperatures. The ether bond provides
(as opposed to esters) hydrolysis resistance as well as some flexibility, which leads to impact strength. In addition, the ether
bond leads to good heat resistance and better flow of the melt.[12]

Applications

Polysulfone has one of the highest service temperatures among all melt-processable thermoplastics. Its resistance to high
temperatures gives it a role of a flame retardant, without compromising its strength that usually results from addition of flame
retardants. Its high hydrolysis stability allows its use in medical applications requiring autoclave and steam sterilization.
However, it has low resistance to some solvents and undergoes weathering; this weathering instability can be offset by adding
other materials into the polymer.

Membranes

Polysulfone allows easy manufacturing of membranes, with reproducible properties and controllable size of pores down to 40
nanometers. Such membranes can be used in applications like hemodialysis, waste water recovery, food and beverage
processing, and gas separation. These polymers are also used in the automotive and electronic industries. Filter cartridges
made from polysulfone membranes offer extremely high flow rates at very low differential pressures when compared with
nylon or polypropylene media.

Polysulfone can be used as filtration media in filter sterilization.

Materials

Polysulfone can be reinforced with glass fibers. The resulting composite material has twice the tensile strength and three time
increase of its Young's modulus.

Fuel cells

Polysulfone is often used as a copolymer. Recently, sulfonated polyethersulfones (SPES) have been studied as a promising
material candidate among many other aromatic hydrocarbon-based polymers for highly durable proton-exchange membranes
in fuel cells.[13] Several reviews have reported progress on durability from many reports on this work.[14] The biggest
challenge for SPES application in fuel cells is improving its chemical durability. Under oxidative environment, SPES can undergo
sulfonic group detachment and main chain scission. However the latter is more dominant; midpoint scission and unzip
mechanism have been proposed as the degradation mechanism depending on the strength of the polymer backbone.[15]

Industrially relevant polysulfones

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Some industrially relevant polysulfones are listed in the following table:

References

^ Kaiser, Wolfgang (2011). Kunststoffchemie für Ingenieure von der Synthese bis zur Anwendung [Plastics chemistry for
engineers from synthesis to application] (in German) (3rd ed.). München: Hanser. p. 461. ISBN 9783446430471. record.

^ Fink, Johannes Karl (2008). High performance polymers. Norwich, NY: William Andrew. pp. 453–481. ISBN 9780815515807.
record.

^ Makromolekulare Chemie : ein Lehrbuch für Chemiker, Physiker, Materialwissenschaftler und Verfahrenstechniker. Lechner,
Manfred D., Gehrke, K., Nordmeier, Eckhard. (4., überarb. und erw. Aufl ed.). Basel [u.a.]: Birkhäuser. 2010. p. 134. ISBN
9783764388904. OCLC 643841472.

^ a b GB, H.A. Vogel, "Polyarylsulphone polymers"

^ GB, Alford G. Farnham, Robert N. Johnson, "Polyarylene Polyethers"

^ GB, Barr Dennis Arthur; Rose John Brewster, "Production of Aromatic Polymers and Intermediates therefor"

^ a b Rose, J. B. (July 1974). "Preparation and properties of poly(arylene ether sulphones)". Polymer. 15 (7): 456–465.
doi:10.1016/0032-3861(74)90111-6.

^ a b David Parker, Jan Bussink, Hendrik T. van de Grampel, Gary W. Wheatley, Ernst-Ulrich Dorf, Edgar Ostlinning, Klaus
Reinking, "Polymers, High-Temperature" in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH: Weinheim.
doi:10.1002/14356007.a21_449