## Abstract Functional macroporous polymers have been synthesized from copolymers of trimethylolpropane trimethacrylate (TRIM) and glycidyl methacrylate (GMA). The accessibility of the epoxy groups has been investigated by reaction with dialkylamines and diamines of different chain lengths. The obt
Gelation in the copolymerization of methyl methacrylate with trimethylolpropane trimethacrylate
โ Scribed by Akira Matsumoto; Hiroyuki Ando; Masayashi Oiwa
- Book ID
- 103076219
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 343 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0014-3057
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โฆ Synopsis
Three-dimensional network formation in the copolymerization of methyl methacrylate with trimethylolpropane trimethacrylate (TMPMA) is discussed. In order to clarify structural features of the copolymer, the cyclization constant of TMPMA was estimated to be K c = 4.2 mol/l and thus, the TMPMA units incorporated into the primary chain consisted of 18% noncyclic and 82% monocyclic structures for a typical copolymer. The gel points obtained under various polymerization conditions depended more significantly on dilution than on the amount of crosslinker. The molecular weight and intrinsic viscosity data suggest the occurrence of intramolecular cyclization leading to the formation of loop structures which was confirmed by GPC-LALLS measurement. Solution properties of the resulting copolymers are discussed in connection with the occurrence of intramolecular crosslinking which becomes more significant with the progress of polymerization.
๐ SIMILAR VOLUMES
Methyl methacrylate was radically copolymerized with oligoglycol dimethacrylate using dioxane or n-butyl acetate as good and poor solvents, respectively. The delay between actual gel point and the theoretical one was much larger in a good solvent. The primary chain length, closely related to gelatio
Copolymerizations of methyl methacrylate with the Li, Na and K salts of methacrylic acid have been studied in methanol solution at 60 ยฐ . Reactivity ratios have been calculated by the methods due to Mayo and Lewis, Fineman and Ross and Peckham. The rate of copolymerization decreases as the size of t