Page 101 - Handbook of Adhesion Promoters
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94                                    Polymer Modification to Improve Adhesion





















            Figure 6.1. Carboxylic group interactions (a) at acidic pH where there are hydrogen bonds between dimers
            created by COOH, and (b) at basic pH, where there are polar ionomeric domains. [Adapted, by permission, from
            Gurney, RS; Morse, A; Siband, E; Dupin, D; Armes, SP; Keddie, JL, J. Colloid Interface Sci., 448, 8-16, 2015.]
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           located on the neighboring latex particles are minimized.  At high pH, the presence of Na +
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           cations leads to the formation of polar ionomeric domains (Figure 6.1b).  The ionomer
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           domains act as weak physical crosslinkers.
                The  methacrylated  β-cyclodextrins,  having  several  polymerizable  methacrylate
           groups and hydrophilic hydroxyl groups, may promote bonding of dental composites to
                 5
           dentin.  The study indicated that nonacidic methacrylated β-cyclodextrin monomers can
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           be used as adhesion-promoting comonomers.
                Halloysite  nanotubes  were  used  in  nanocomposites  via in situ  polymerization. 6
           Methyl methacrylate was the main monomer copolymerized with a small quantity of ionic
           comonomer  2-(methacryloyloxy)ethyltrimethylammonium  chloride  (MTC)  and  2-acryl-
                                                  6
           amido-2-methylpropane sulfonic acid (AMPS).  Halloysite was added during the polym-
                           6
           erization  process.  The noncovalent interactions between  halloysite  and  ionic
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           comonomers are key factors of successful preparation of nanocomposites.  The nanocom-
           posites demonstrated excellent mechanical performance due to a strong interfacial adhe-
           sion ameliorated by noncovalent interactions enhanced by electrostatic attraction between
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           the positively charged matrix of the ionic copolymer and negatively charged halloysite.
                The monomer 2-acetoacetoxy ethyl methacrylate was used as a complexing unit to
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           produce copper(II) complexes in the coating’s upper surface layer.  The copper(II) com-
           plexes were stable against washing out and provided biofouling protection to glass and
                        7
           metal  surfaces.   The  copper-loaded  complexes  reduced  the  growth  of  Achnanthidium
                                      7
           spec. and Staphylococcus aureus.
                Because of the polarity of comonomers, the ethylene copolymers, such as Lupolen V
           and Lucalen, can be welded and bonded more readily by adhesives than the homopoly-
                8
           mers.  The low adhesion of polyethylene requires surface pretreatment or copolymeriza-
           tion  of  ethylene  with  small  amounts  of  polar  comonomers  which  act  as  adhesion
                    9
           promoters.  The ethylene copolymers with 10-undecenoic acid and with 5,7-dimethylocta-
                                   9
           1,6-diene  were  synthesized.   Both  exhibit  higher  adhesion  strengths  with  increasing
                             9
           comonomer contents.  The 10-undecenoic acid/ethylene copolymers are more effective in
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           improving adhesion because of their higher polarity.  Propylene was copolymerized with
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