Page 30 - Handbook of Adhesion Promoters
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2.7 Crystalline properties                                            23

























           Figure 2.20. Schematic illustration of the interphase formation between PP and GF. [Adapted, by permission,
           from Luo, G; Li, W; Liang, W; Liu, G; Ma, Y; Niu, Y; Li, G, Compos. Part B: Eng., 111, 190-9, 2017.]
                                                    40
            transfer  between  the  glass  fiber  and  the  matrix.   A  schematic  mechanism  including
                                                                         40
            molecular interaction and polymer chain motion is illustrated in Figure 2.20.  When poly-
            propylene is melted, the compatibilizer (maleic anhydride) chains move to the surface of
            glass fiber because they have shorter relaxation time and diffuse much faster than the lon-
                     40
            ger chains.  The diffusion of the shorter chains also drives the movement of the longer
                                                      40
                                                 chains.   The  nucleating  agent  increases
                                                 crystallization and contributes to the forma-
                                                                         40
                                                 tion  of  transcrystalline  layer.  The  diffu-
                                                 sivity of polymer chains and the interaction
                                                 between matrix and glass fiber are key fac-
                                                 tors  for  the  formation  of  the  interface,
                                                 which  has  dominating  effects  on  the
                                                                                 40
                                                 mechanical properties of the composite.
                                                     Polyamide-66, an aliphatic semicrys-
                                                 talline  polyamide,  was  reinforced  with  E-
                                                 glass  fibers  and  high-modulus  carbon
                                                      41
                                                 fibers.   An  interphase  was  composed  of
            Figure 2.21. The transcrystalline interphase in a high-  transcrystallinity developed due to the high
            modulus carbon-fiber-reinforced polyamide-66 com-  nucleation  density  of  the  polymer  on  the
            posite (unsized carbon fiber embedded in a polyamide-  fiber  surface  (Figure  2.21).   Composites
                                                                        41
            66 matrix melt-crystallized at 235°C). [Adapted, by per-
            mission, from Clark, RL; Kander, RG; Sauer, BB, Com-  containing  transcrystallinity  have  higher
            pos. Part A: Appl. Sci. Manufact., 30, 1, 27-36, 1999.]  interfacial shear strength values than those
                                                                            41
                                                 that do not contain this interphase.
                Short glass fiber was coated with electrically conducting polyaniline by in situ chem-
                            42
            ical polymerization.  The coated fiber was melt-compounded with isotactic polypropyl-
                                                                  42
            ene  grafted  with  maleic  anhydride  as  an  adhesion  promoter.   Scanning  electron
            microscopy showed the improvement in wetting and dispersion of the fibers when the
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