Page 80 - Handbook of Adhesion Promoters
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4.2 Surface treatment                                                 73

































            Figure 4.22. The reaction scheme of the chemical modifications in step 1 and 2. Additional wavenumbers are
            depicted for the most important characteristic infrared bands. [Adapted, by permission, from Schaubroeck, D;
            De Baets, J; Desmet, T; Van Vlierberghe, S; Schacht, E; Van Calster, A, Appl. Surf. Coat., 255, 21, 8780-7, 2009.]


            rimethoxysilane,  MPTMS,  and  poly(diallyldimethylammonium)  chloride,  PDDA,
            improve adhesion of hydrogen silsesquioxane to gold, the 3-aminopropyltriethoxysilane,
            APTES,  enhances  its  adhesion  on  Mo  substrates  with  polydiallyldimethylammonium
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            chloride and it improves adhesion to Si, Cr, Cu and ITO (Figure 4.21).  This is one of the
            typical uses of adhesion promoters discussed throughout this book.
                Cellulose fibers from sugar cane were modified using octadecanoyl and dodecanoyl
                        55
            chloride  acids.   The  surface  chemical  modification  of  cellulose  fibers  resulted in
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            improved interfacial adhesion with the polyethylene matrix and higher dispersion level.
                Treatment of polyvinylfluoride and polyvinylidenefluoride with hot aqueous solu-
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            tions of potassium hydroxide resulted in a large increase in adhesion.  Elimination reac-
                                                                         56
            tions  occurred  in  PVDF,  since  C  C =    and  C  C ≡    bonds  were  present.   Substantial
            chemical modification of PVF did not result in a large increase in adhesion which is attrib-
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            uted to the chemical modification of a weak boundary layer without its removal.
                The introduction of amine groups on the surface of dielectric resins improves the
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            adhesion with electrochemically deposited metals.  The etched epoxy resin surfaces were
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            modified with aliphatic amines via a two step chemical reaction (Figure 4.22).  Cyanuric
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            chloride is introduced on the surface, followed by reaction with aliphatic polyamine.
                Wet-chemical modification reactions with nucleophilic reactants (thiophenol or pyri-
            dine groups introduced) were employed to introduce groups of different chemical nature
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            onto the PVC surface resulting in a reduction of bacterial adhesion to PVC.
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