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 Encyclopedia of Physical Science and Technology  EN008C-602  July 25, 2001  20:31







              Macromolecules, Structure                                                                   863

              TABLE II  Trade Names of Selected Polymers
              ABS         Acrylonitrile–butadiene–styrene graft copolymers
              Acrylic     Poly(acrylonitrile)
              Amberlite   Ion-exchange resins
              Bakelite    Phenol-formaldehyde
              Buna N      Butadiene–acrylonitrile copolymer
              Buna S (SBR)  Butadiene–styrene copolymer
              Butyl rubber  Poly(isobutylene)  + ∼1% isoprene
              Carbowax    Poly(ethylene glycol)
              Cellophane  Cellulose hydrate
              Celluloid   Cellulose nitrate
              Cycolac     ABS
              Dacron      Poly(ethylene terephthalate) fiber
                                                                FIGURE  2  Examination  of  the  chemical  details  in  branched
              Delrin      Poly(oxymethylene)
                                                                polyethylene. Within the magnifying glass, the large balls repre-
              Dynel       Vinyl chloride–acrylonitrile copolymer  sent carbon atoms and the small ones are the hydrogen atoms.
              Epon        Epoxy resin                           The four-carbon segment is a butyl branch.
              Estane      Polyurethane
              HIPS        High-impact polystyrene—copolymer of styrene  C.  Formation of Macromolecules
                           and butadiene
              Hytrel      Poly(butylene terephthalate)–poly(butylene glycol)  As  an  introduction  to  the  understanding  of  structure,
                           copolymer                            we must first consider the formation of macromolecules.
              Kapton      Polyimide                             Polymer formation involves either chain or step reactions,
              Kel-F       Poly(chlorotrifluoroethylene)          or living polymerization. Earlier, the terms addition and
              Kevlar      Polyaramide fiber                      condensation, respectively, were used to describe chain
              Lexan       Polycarbonate                         and step growth polymerization. One important difference
              Lucite      Poly(methyl methacrylate)             between the mechanisms is shown in Fig. 3, which shows
              Marlex      Polyethylene                          a plot of the polymer molecular weight versus monomer
              Mylar       Polyester film                         consumption. In step polymerization, once the chain is ini-
              Neoprene    Poly(chloroprene)                     tiated monomer molecules add in rapid succession to the
              Orlon       Poly(acrylonitrile)                   reactive end group of the growing polymer chain until it
              Plexiglas   Poly(methyl methacrylate)             terminates and becomes unreactive. In the growth or prop-
              PPO         Poly(2,6-dimethyl phenylene oxide)    agation step, several thousand monomer units add one at
              PVC         Poly(vinyl chloride)                  a time to each growing chain in a time interval of less than
              Rayon       Fibers from regenerated cellulose     1 sec. Thus, at any stage of a chain polymerization, the re-
              Ryton       Polyphenylene sulfide                  acting system in effect consists of two species: monomers
              SBR         (See Buna S)                          and very large molecular weight polymers. The forma-
              Silicone    Dialkyl siloxanes                     tion of polystyrene from styrene is an example of chain
              Spandex     Fibers from elastic polyurethanes     polymerization.
              Styrofoam   Polystyrene
              Teflon       Poly(tetrafluoroethylene)
              Viton       Vinylidene fluoride–hexafluoropropylene copolymer




              composed of two or more monomer units and can occur
              in random, alternating, block or graft copolymers.
                Figure  2  schematically  illustrates  the  next  level  of
              detail—the chemical structure of the monomer unit. The
              polymer in this drawing is polyethylene, composed mainly
              of  repeating  (CH 2 )  units.  The  main  chain  and  a  butyl
              branch  are  shown  under  the  magnifying  glass.  (Butyl
                                                                FIGURE 3 The dependence of molecular weight on monomer
              branches occur at the level of approximately 1 per 100 CH 2  conversion for (A) chain polymerization, (B) step polymerization,
              groups.)                                          and (C) living polymerization.
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