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High-molecular-weight polyacrylonitrile by atom transfer radical polymerization

✍ Scribed by Chen Hou; Rongjun Qu; Junshen Liu; Liang Ying; Chengguo Wang


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
81 KB
Volume
100
Category
Article
ISSN
0021-8995

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✦ Synopsis


Abstract

A single‐pot atom transfer radical polymerization was used for the first time to successfully synthesize polyacrylonitrile with a molecular weight higher than 80,000 and a narrow polydispersity as low as 1.18. This was achieved with CuBr/isophthalic acid as the catalyst, 2‐bromopropionitrile as the initiator, and N,N‐dimethylformamide as the solvent. The effects of the solvent on the polymerization of acrylonitrile were also investigated. The induction period was shorter in N,N‐dimethylformamide than in propylene carbonate and toluene, and the rate of the polymerization in N,N‐dimethylformamide was fastest. The molecular weight of polyacrylonitrile agreed reasonably well with the theoretical molecular weight in N,N‐dimethylformamide. When chlorine was used in either the initiator or the catalyst, the rate of polymerization showed a trend of decreasing, and the molecular weight deviated from the theoretical predication significantly. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3372–3376, 2006


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A kinetic model has been developed for atom transfer radical polymerization processes using the method of moments. This model predicts monomer conversion, number-average molecular weight and polydispersity of molecular weight distribution. It takes into account the effects of side reactions includin