Poly(ether sulfones)




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Poly(ether sulfones) PES for short, are high performance polymers. The most popular is one made by Union Carbide called UdelTM. That's the one you see in the picture at the top of the page. Poly(ether sulfones) act a lot like polycarbonates, but they're a lot more heat resistant.

Poly(ether sulfones) also can stand up well to water and steam, so they're used to make things like cookware and medical products that need to be sterilized between uses.

Poly(ether sulfones get their name because they have ether groups and sulfone groups in their backbone chains. PES polymers have high glass transition temperatures, or Tg's, because the sulfone groups are so stiff. In fact, poly(phenyl sulfone) is so stiff that it doesn't have a glass transition temperature! It stays hard as a rock right up until it decomposes at around 500 oC.

This is bad. This means that it can't be processed. In order to make it processable, we have to make that chain a little more flexible so the polymer will soften at a reasonable temperature. We do this by putting flexible groups in the backbone chain, namely ether linkages.

UdelTM uses a bisphenol A derived linkage to make the chain flexible. You'll notice that this polymer has two ether linkages in the repeat unit. For this reason UdelTM is more properly called a poly(ether ether sulfone).

We call this a bisphenol A linkage because it's based on the monomer bisphenol A, but more about that later.

This brings the Tg down to 190oC. By playing around and using different kinds of flexible groups we can alter the Tg further. If we use a less flexible linkage, the Tg jumps to 230 oC.

This PES is made by Imperial Chemical Industries (ICI), and they call it by the romantic name of Polyether Sulfone 200 PTM. You'll notice that unlike UdelTM, this polymer has only one ether linkage between sulfone groups. This makes the chain stiffer and the Tg higher.

But you ask, "How do we make a wonderful poly(ether sulfone)?" Like this: One reacts the sodium salt of bisphenol A (remember bisphenol A?) and reacts it with di-para-fluorophenylsulfone in a solvent like dimethylsulfoxide (DMSO) at between 130 and 160 oC and that gets us a poly(ether sulfone)!

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