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A chain geometry prediction of polystyrene and polyarylate block copolymer by a kinetic simulation model
Author(s) -
Ohishi Hiroshi,
Nishi Toshio
Publication year - 2000
Publication title -
journal of polymer science part a: polymer chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.768
H-Index - 152
eISSN - 1099-0518
pISSN - 0887-624X
DOI - 10.1002/(sici)1099-0518(20000115)38:2<299::aid-pola4>3.0.co;2-x
Subject(s) - copolymer , polystyrene , polymer chemistry , materials science , kinetics , polymerization , block (permutation group theory) , chemistry , geometry , composite material , polymer , mathematics , physics , quantum mechanics
The chain geometry of polystyrene (PS) and polyarylate (PAr) block copolymer was predicted by the simulation of the kinetics of the block‐copolymerization route. The simulation model consisted of a combination of two models. In the first model, the kinetics of the free‐radical polymerization of carboxyl‐terminated telechelic PS (COOH‐PS‐COOH) was simulated for the determination of the molecular weight distribution. In the second model, the kinetics of the PS and PAr block copolymerization with COOH‐PS‐COOH was simulated by a Monte Carlo computation, with each reacting functional group assigned by an integer. The number‐average and weight‐average molecular weights and the composition of the PS‐PAr block copolymer, as calculated by the simulation models, were in good agreement with the experimental data. From this agreement, plausible predictions for the chain geometry (i.e., the type of block copolymer and length of each segment) were obtained that were practically impossible to analyze experimentally. The simulation results showed that more than 80 wt % of the block copolymer synthesized by this method was a composite of various types of multiblock copolymers and that the length of the PAr segment was almost the same as that of the homo‐PAr obtained as a by‐product. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 299–309, 2000

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