Monomer reactivity ratios for acrylonitrile-methyl acrylate free-radical copolymerization

被引:47
|
作者
Wiles, KB
Bhanu, VA
Pasquale, AJ
Long, TE
McGrath, JE
机构
[1] Virginia Polytech Inst & State Univ, Dept Chem, Blacksburg, VA 24061 USA
[2] Virginia Polytech Inst & State Univ, Coll Sci, Mat Res Inst, Blacksburg, VA 24061 USA
关键词
reactivity ratios; acrylonitrile; methyl acrylate; in situ FT-IR; nonlinear analysis;
D O I
10.1002/pola.20149
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Nonlinear monomer reactivity ratios for the homogeneous free-radical co-polymerization of acrylonitrile and methyl acrylate were determined from H-1 NMR and real-time Fourier transform infrared (FTIR) analyses. All H-1 NMR data were obtained on polymers isolated at low conversions (<10%), whereas the FTIR data were collected in situ. The copolymerizations were conducted in N,N-dimethylformamide at 62 degreesC and were initiated with azobisisobutyronitrile. The real-time FTIR technique allowed for many data points to be collected for each feed composition, which enabled the calculation of copolymer compositions (dM(1)/dM(2)) with better accuracy. Monomer reactivity ratios were estimated with the Mayo-Lewis method and then were refined via a nonlinear least-squares analysis first suggested by Mortimer and Tidwell. Thus, monomer reactivity ratios at the 95% confidence level were determined to be 1.29 +/- 0.2 and 0.96 +/- 0.2 for acrylonitrile and methyl acrylate, respectively, which were valid under the specific system conditions (i.e., solvent and temperature) studied. The results are useful for the development of acrylonitrile (<90%) and methyl acrylate, melt-processable copolymer fibers and films, including precursors for carbon fibers. (C) 2004 Wiley Periodicals, Inc.
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页码:2994 / 3001
页数:8
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