کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1397001 | 984208 | 2006 | 6 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Kinetics of copolymerization and degradation of poly[acrylonitrile-co-(amino ethyl-2-methyl propenoate)]
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی آلی
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: Kinetics of copolymerization and degradation of poly[acrylonitrile-co-(amino ethyl-2-methyl propenoate)] Kinetics of copolymerization and degradation of poly[acrylonitrile-co-(amino ethyl-2-methyl propenoate)]](/preview/png/1397001.png)
چکیده انگلیسی
Amino ethyl-2-methyl propenoate was firstly used to successfully copolymerize with acrylonitrile in a H2O/dimethylsulfoxide (DMSO) mixture between 50 °C and 70 °C under N2 atmosphere. This was achieved by using azobisisobutyronitrile as the initiator. Kinetics of copolymerization of acrylonitrile with amino ethyl-2-methyl propenoate was investigated. The kinetic equation of copolymerization was obtained and the apparent activation energy of degradation of poly[acrylonitrile-co-(amino ethyl-2-methyl propenoate)] was determined. Increasing DMSO concentration in the solvent mixture leads to a rapid increase in the degradation apparent activation energy. The apparent activation energy decreases quickly with an increase in the comononer amino ethyl-2-methyl propenoate concentration, and such a change becomes less prominent as the molar ratio of amino ethyl-2-methyl propenoate/acrylonitrile goes beyond 2/100. The apparent activation energy also increases along with the copolymerization temperature. The resultant fibers prepared from poly[acrylonitrile-co-(amino ethyl-2-methyl propenoate)] were obtained with the fineness at 1.03 dtex and the tenacity at 6.18cN dtexâ1.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: European Polymer Journal - Volume 42, Issue 5, May 2006, Pages 1093-1098
Journal: European Polymer Journal - Volume 42, Issue 5, May 2006, Pages 1093-1098
نویسندگان
Chen Hou, Chunnuan Ji, Rongjun Qu, Chunhua Wang, Chengguo Wang,