Page 332 - Engineering Plastics Handbook
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290   Engineering Plastics

        It was produced by using the aromatic nucleophilic polycondensation reac-
        tion of bisphenol A with 4,4′-dichlorodiphenylsulfone, a process still used
        today by the commercial producers of this polymer. This polymer, known
        as polysulfone (PSF), has a glass transition temperature of about 185°C.
        It is the oldest and most widely utilized member of the family of sulfone
        polymers. Polysulfone and all the commercially available sulfone poly-
        mers are completely amorphous and transparent in their natural state.
        They have high glass transition temperatures T ranging from 185 to
                                                     g
        265°C. The high heat resistance derived from the high T ’s, along with the
                                                          g
        high thermal oxidative resistance derived from the aromatic backbone
        structure, allows use of these polymers in demanding high-performance
        applications where high temperatures are encountered for long durations.
        In addition to the high-temperature capability, the sulfone polymers boast
        outstanding hydrolytic stability as another of their chief performance fea-
        tures. In the early 1980s, the second of the commercially important sul-
        fone polymers,  polyethersulfone (PES), was introduced by Imperial
        Chemical Industries in the United Kingdom. This polymer has the fol-
        lowing repeat unit structure:
                                      O
                                      S         O
                                      O
        which is sometimes also depicted in the form

                                O                   O
                     O          S         O         S
                                O                   O
        to reflect the polymer’s chemical synthesis from the polycondensation of
        4,4′-dichlorodiphenylsulfone and 4,4′-dihydroxydiphenylsulfone. This poly-
        mer extended the temperature capability of sulfone polymers by offering
        a glass transition temperature of 220°C.
          In 1990, Amoco Performance Products, Inc., introduced an even
        higher-performance sulfone polymer derived from the condensation
        polymerization of 4,4′-dichlorodiphenylsulfone with 4,4′-dihydroxy-
        diphenyl (also known as biphenol). This polymer, which came to be
        known as polyphenylsulfone (PPSF) and which was introduced com-
                                           ®
        mercially under the trade name Radel R, has the following repeat unit
        structure:
                                                   O
                      O                  O         S
                                                   O
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