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Epoxy resin/acrylic composite latexes: reactivity and stability of epoxy groups with carboxyl groups
Affiliation:1. POLYMAT, Kimika Aplikatua saila, Kimika Fakultatea, University of the Basque Country UPV/EHU, Joxe Mari Korta Zentroa, Tolosa Hiribidea 72, 20018 Donostia-San Sebastián, Spain;2. CIDETEC, Parque Científico y Tecnológico de Gipuzkoa, Po. Miramón 196, 20014 Donostia-San Sebastian, Spain;3. POLYMAT, Polymer Science and Technology Department, Faculty of Chemistry, University of the Basque Country (UPV/EHU), 20018 Donostia-San Sebastian, Spain;1. School of Chemical and Environmental Engineering, Wuhan Polytechnic University, Wuhan, Hubei, China;2. Department of Physics, M. V. Lomonosov Moscow State University, Leninskie gory 1/2, 119991 Moscow, Russia;3. Oil Crops Research Institute, Chinese Academy of Agricultural Sciences, Key Laboratory of Oilseeds Processing, Ministry of Agriculture, Hubei Key Laboratory of Lipid Chemistry and Nutrition, Wuhan, Hubei, China
Abstract:Epoxy resin (Ep850)/acrylic composite latex was prepared by the miniemulsion polymerization method. Epoxy-functionalized latex made by the miniemulsion polymerization process with Ep850 was compared with that made by the conventional emulsion polymerization process with glycidyl methacrylate (GMA). The reactivity and stability of epoxy groups were investigated in the latexes and films, and quantified by Fourier transform-IR spectrometry. The solvent resistance of films strongly correlated with the residual epoxy groups in latex. The epoxy groups originating from Ep850 in the miniemulsion process were less reactive than those from GMA in the conventional process. Almost all epoxy groups originating from Ep850 in the miniemulsion method were remained even after its polymerization, whereas about 25% of the epoxy groups originating from GMA were lost during the polymerization. When the storage temperature was kept at 50° C, almost all of the epoxy groups in both methods were lost quickly. Most of the epoxy groups in the miniemulsion method were gradually lost at 5° C by cross-linking with carboxyl groups during storage, whereas most of the epoxy groups obtained in the conventional method were gradually lost by hydrolysis. Their differences in reactivity or stability were considered to be due to the difference in hydrophilicity, molecular weight or polymerization method.
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