Polymerization of bismaleimide by Michaeladdition using barbituric acid as nucleophile
碩士 === 國立臺北科技大學 === 有機高分子研究所 === 97 === In this study, bismaleimide (BMI) and barbituric acid (BTA) were used as monomer to synthesize a new type of polymeric material. Traditional 1H and 13C nuclear magnetic resonance and two dimensional techniques, and so COSY, HSQC, HMBC were employed to analyze...
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ndltd-TW-097TIT053101022019-08-16T03:39:28Z http://ndltd.ncl.edu.tw/handle/z23mb2 Polymerization of bismaleimide by Michaeladdition using barbituric acid as nucleophile 研究利用巴比妥酸當親核劑與雙馬來醯亞胺進行麥克加成聚合反應 Jia-Wei Shiu 徐嘉偉 碩士 國立臺北科技大學 有機高分子研究所 97 In this study, bismaleimide (BMI) and barbituric acid (BTA) were used as monomer to synthesize a new type of polymeric material. Traditional 1H and 13C nuclear magnetic resonance and two dimensional techniques, and so COSY, HSQC, HMBC were employed to analyze the chemical structure of the thus-synthesized polymer products. Meanwhile, dependence of molecular weight on the reaction time was investigate via gel permeation chromatography (GPC). Basically, it increased with reaction time linearly and the final product had a molecular weight around ten thousands with a polydispersity index (PDI) of 2 ~ 4. Additionally, the MALDI-TOF mass spectrum clearly indicated a molecular mass of 476 dalton for the repeat unit in the polymer, suggest both BMI and BTA were monomer and the polymerization were carried out by the Michael addition using BTA as nucleophile. Furthermore the data from evolved gas analysis (EGA) and thermalgravimetric analyzer (TGA) both BMI and BTA were the constitute of the final polymer. Syang-Peng Rwei 芮祥鵬 2009 學位論文 ; thesis 80 zh-TW |
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碩士 === 國立臺北科技大學 === 有機高分子研究所 === 97 === In this study, bismaleimide (BMI) and barbituric acid (BTA) were used as monomer to synthesize a new type of polymeric material. Traditional 1H and 13C nuclear magnetic resonance and two dimensional techniques, and so COSY, HSQC, HMBC were employed to analyze the chemical structure of the thus-synthesized polymer products. Meanwhile, dependence of molecular weight on the reaction time was investigate via gel permeation chromatography (GPC). Basically, it increased
with reaction time linearly and the final product had a molecular weight around ten thousands with a polydispersity index (PDI) of 2 ~ 4. Additionally, the MALDI-TOF mass spectrum clearly indicated a molecular mass of 476 dalton for the repeat unit in the polymer, suggest both BMI and BTA were monomer and the polymerization were carried out by the Michael addition using BTA as nucleophile. Furthermore the data from evolved gas analysis (EGA) and thermalgravimetric analyzer (TGA) both BMI and BTA were the constitute of the final polymer.
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author2 |
Syang-Peng Rwei |
author_facet |
Syang-Peng Rwei Jia-Wei Shiu 徐嘉偉 |
author |
Jia-Wei Shiu 徐嘉偉 |
spellingShingle |
Jia-Wei Shiu 徐嘉偉 Polymerization of bismaleimide by Michaeladdition using barbituric acid as nucleophile |
author_sort |
Jia-Wei Shiu |
title |
Polymerization of bismaleimide by Michaeladdition using barbituric acid as nucleophile |
title_short |
Polymerization of bismaleimide by Michaeladdition using barbituric acid as nucleophile |
title_full |
Polymerization of bismaleimide by Michaeladdition using barbituric acid as nucleophile |
title_fullStr |
Polymerization of bismaleimide by Michaeladdition using barbituric acid as nucleophile |
title_full_unstemmed |
Polymerization of bismaleimide by Michaeladdition using barbituric acid as nucleophile |
title_sort |
polymerization of bismaleimide by michaeladdition using barbituric acid as nucleophile |
publishDate |
2009 |
url |
http://ndltd.ncl.edu.tw/handle/z23mb2 |
work_keys_str_mv |
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