Page 581 - Handbook of Thermal Analysis of Construction Materials
P. 581

Section 2.0 - Adhesives and Sealants                         551



                                             —  —  CH 2  –  CCH 3  –  CH 2  –  CH  —  —
                                                                            
                                                         |            |     
                                                  RO  – C =  O  RO  – C = O  n 

                                                          acrylic copolymer

                              where R = –CH , –CH –CH ,  –CH –(CH ) .
                                                             2
                                                                   3 2
                                            3
                                                       3
                                                  2
                                     The adhesive properties of polymers produced by solvent polymer-
                              ization are better than those produced from emulsion polymerization.
                              Acrylic sealants set by solvent evaporation, have good adhesion, excellent
                              flexibility, good heat and chemical and ozone resistance. [23]  However, they
                              shrink upon evaporation of the solvent and upon aging. Acrylic sealants are
                              not recommended for joints exposed to contraction and expansion.
                                     Polychloroprenes. The structure of the polychloroprene chain can
                              be represented as shown below: [23]


                                         (–CH –CCl=CH–CH –) –
                                                              n
                                                            2
                                              2
                                     Polychloroprene is commercially produced by emulsion poly-
                              merization and exists as a one- and two-component system. The one-
                              component polychloroprene sets to touch in 4–6 hours and cures slowly (3–
                              7 days). [23]  The two-component system is a solvent-free, non-shrinking,
                                                                               [3]
                              slump resistant sealant which sets quickly, but cures slowly.  Polychloroprene
                              sealants have poor color retention (usually are pigmented with black
                              pigments), and high shrinkage.
                                     Polyisobutene and Butyl Rubber.  Polyisobutene, referred to
                              sometimes as polyisobutylene, is considered the precursor of butyl rubber
                              and is processed by low temperature cationic polymerization of isobuty-
                              lene. The chemical structure can be represented as: [3]

                                                                                   ⋅⋅⋅⋅⋅
                                     ⋅⋅⋅⋅⋅  2     3 2    2      3  2 n    2      3 2 ⋅⋅⋅⋅⋅
                                     ⋅⋅⋅⋅⋅
                                     ⋅⋅⋅⋅⋅
                                                                                   ⋅⋅⋅⋅⋅
                                                                                   ⋅⋅⋅⋅⋅
                                     ⋅⋅⋅⋅⋅
                                     ⋅⋅⋅⋅⋅CH –C(CH ) –[CH –C(CH –) ] –CH –C(CH ) ⋅⋅⋅⋅⋅
                                     Since this polymer is 100% saturated, it cannot be converted to a
                              practical elastomer nor vulcanized by normal means. To overcome the lack
                              of unsaturation, isobutene is copolymerized with a small amount of a diene
                              monomer. The resulting polymer is vulcanized by sulfur-based systems.
                                     ⋅⋅⋅⋅⋅–[–CH –C(CH ) –] –CH –CCH =CH–CH –⋅⋅⋅⋅⋅
                                                     3 2
                                                                              2
                                                              2
                                              2
                                                                    3
                                                         n
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