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Kinetics of diffusion in polyacrylonitrile fiber formation
Author(s) -
Hou Chen,
Qu Rongjun,
Liang Ying,
Wang Chengguo
Publication year - 2005
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.21526
Subject(s) - polyacrylonitrile , acrylonitrile , diffusion , dimethyl sulfoxide , polymer chemistry , polymerization , solvent , materials science , chemistry , aqueous solution , chemical engineering , copolymer , polymer , organic chemistry , thermodynamics , physics , engineering
Abstract A H 2 O/dimethyl sulfoxide (DMSO) mixture was used as the coagulation bath of the wet‐spun process for polyacrylonitrile fibers. Diffusion behaviors of coagulate and solvent of the protofibers were studied. Diffusion coefficients of H 2 O and DMSO of the protofibers, prepared by acrylonitrile (AN) homopolymers, were also determined. It was found that diffusion coefficients of H 2 O and DMSO in the protofibers prepared by AN homopolymers, synthesized by DMSO solution polymerization, are highest compared with those of AN homopolymers synthesized by H 2 O/DMSO mixture suspension polymerization and aqueous suspension polymerization. With increasing polyacrylonitrile concentration in the dope, diffusion coefficients of H 2 O and DMSO decreased continuously. Diffusion coefficients of H 2 O and DMSO increased concomitantly with increasing bath temperature, but the changes of diffusion coefficient values were less prominent when the temperature increased beyond 60°C. When DMSO concentration in the coagulation bath was 55 wt %, the values of diffusion coefficients of H 2 O and DMSO were minimal. Diffusion coefficients increased with increasing jet stretch minus ratio. When the protofiber radius was increased, there was a corresponding increase of diffusion coefficients of H 2 O and DMSO. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1529–1533, 2005