2000Journal of Applied Polymer ScienceRequires access

Tacticity of methacrylic copolymers and their crosslinked polymers studied by pyrolysis-gas chromatography

Masaaki Kiura, Jun-Ichiro Atarashi, Kiyoshi Ichimura, Hajime Ito, Hajime Ohtani, Shin Tsuge

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Abstract

Diad tacticity of methyl methacrylate (MMA) sequences in the copolymers of MMA and various acrylates and their crosslinked polymers was characterized by pyrolysis–gas chromatography (Py-GC) based on the relative peak intensities of the diastereomeric MMA tetramers in the pyrograms. The diad tacticity in the copolymers synthesized at a given temperature proved to be almost consistent with that of corresponding MMA homopolymers (PMMA) prepared under the same conditions. Furthermore, the diad tacticity of PMMAs was also consistent with that of the corresponding crosslinked polymers. These results suggest that the tacticity of MMA sequences in the polymer chains would be dominated by polymerization temperature, independent of the copolymerization and crosslinking. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 2140–2144, 2000

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Diad tacticity of methyl methacrylate (MMA) sequences in the copolymers of MMA and various acrylates and their crosslinked polymers was characterized by pyrolysis–gas chromatography (Py-GC) based on the relative peak intensities of the diastereomeric MMA tetramers in the pyrograms. The diad tacticity in the copolymers synthesized at a given temperature proved to be almost consistent with that of corresponding MMA homopolymers (PMMA) prepared under the same conditions. Furthermore, the diad tacticity of PMMAs was also consistent with that of the corresponding crosslinked polymers. These results suggest that the tacticity of MMA sequences in the polymer chains would be dominated by polymerization temperature, independent of the copolymerization and crosslinking. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 2140–2144, 2000

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Available abstract

Diad tacticity of methyl methacrylate (MMA) sequences in the copolymers of MMA and various acrylates and their crosslinked polymers was characterized by pyrolysis–gas chromatography (Py-GC) based on the relative peak intensities of the diastereomeric MMA tetramers in the pyrograms. The diad tacticity in the copolymers synthesized at a given temperature proved to be almost consistent with that of corresponding MMA homopolymers (PMMA) prepared under the same conditions. Furthermore, the diad tacticity of PMMAs was also consistent with that of the corresponding crosslinked polymers. These results suggest that the tacticity of MMA sequences in the polymer chains would be dominated by polymerization temperature, independent of the copolymerization and crosslinking. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 2140–2144, 2000

Key concepts: Diad, Tacticity, Copolymer, Polymer chemistry, Polymer, Materials science, Methyl methacrylate, Polymerization

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