期刊文献+
共找到2篇文章
< 1 >
每页显示 20 50 100
Thermal Degradation Kinetics of Structurally Diverse Poly(bispropargyl ethers-bismaleimide) Blends 被引量:1
1
作者 Jeyaraj Pandiyan Dhanalakshmi Mahendran Arunjunai Raj Chinnaswamy Thangavel Vijayakumar 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2016年第3期253-253,254-267,共15页
Structurally diverse bispropargyl ethers using resorcinol,quinol,4,4¢-dihydroxy biphenyl,bisphenol-A,4,4¢-dihydroxy diphenyl ketone,4,4¢-dihydroxy diphenylsulphone,trimethyl indane bisphenol and tetramethyl spirobi... Structurally diverse bispropargyl ethers using resorcinol,quinol,4,4¢-dihydroxy biphenyl,bisphenol-A,4,4¢-dihydroxy diphenyl ketone,4,4¢-dihydroxy diphenylsulphone,trimethyl indane bisphenol and tetramethyl spirobiindane bisphenol were prepared by using phase transfer catalyst.Synthesized materials were separately blended with 4,4¢-bismaleimido diphenyl methane(BMIM)in mole ratios(0.5:0.5).The materials were thermally cured and the structural characterisation and the thermal properties of these cross-linked materials are investigated using Fourier-transform infrared(FTIR)spectrophotometer and thermogravimetric analyzer(TGA).Among the different materials investigated poly MRPE,poly MBPEBPA and poly MSPE show higher onset degradation temperature of 300°C indicating higher thermal stability.The degradation kinetics is investigated using Flynn-Wall-Ozawa(FWO),Vyazovkin(VYZ)and Friedman(FRD)methods.Amongst the various cured materials investigated,the activation energy(Ea-D)values obtained for poly MRPE and poly MKPE were observed to increase continuously froma=0.2 to 0.8 and the values range from 199 kJ/mol to 245 k J/mol and 153 k J/mol to 295 k J/mol respectively.The crosslinked materials resulting from these bispropargyl monomers definitely need more energy for bond cleavage due to the presence of more aromatic units.The volatile products obtained during the thermal degradation of the polymers were analyzed using thermogravimetric-Fourier transform infrared analyses(TG-FTIR).The phenols,substituted phenols,carbon monoxide,carbon dioxide and small amount of aniline were found to be the major products during thermal degradation of these cured blends. 展开更多
关键词 bispropargyl ethers Bismaleimide TG Degradation kinetics TG-FTIR
原文传递
双酚A二炔丙基醚与4,4′-联苯二苄叠氮的合成及聚合反应研究 被引量:11
2
作者 扈艳红 罗永红 +3 位作者 万里强 齐会民 黄发荣 杜磊 《高分子学报》 SCIE CAS CSCD 北大核心 2005年第4期560-565,共6页
合成了两种单体双酚A二炔丙基醚与4,4′联苯二苄叠氮,研究了一种新的低温聚合体系———双酚A二炔丙基醚与4,4′联苯二苄叠氮在烘箱中的本体聚合行为.通过红外、核磁共振以及质谱、元素分析等表征了单体的结构.利用傅立叶红外技术(FTIR... 合成了两种单体双酚A二炔丙基醚与4,4′联苯二苄叠氮,研究了一种新的低温聚合体系———双酚A二炔丙基醚与4,4′联苯二苄叠氮在烘箱中的本体聚合行为.通过红外、核磁共振以及质谱、元素分析等表征了单体的结构.利用傅立叶红外技术(FTIR)跟踪了聚合反应过程中特征基团的变化,采用差示扫描量热技术(DSC)研究了聚合反应工艺及其动力学,热失重分析(TGA)考察了聚合产物的热稳定性能.通过Kissinger法和0zawa法获得了反应的一些动力学参数.结果表明,双酚A二炔丙基醚与4,4′联苯二苄叠氮易发生1,3偶极环加成聚合反应,在聚合物结构中形成三唑五元环,它们的聚合起始温度在70℃左右,聚合反应的主反应是一级反应,表观活化能ΔE=84.6kJmol,指前因子A=4.865×1010min-1.同时发现,聚合物具有较好的热稳定性能. 展开更多
关键词 双酚A二炔丙基醚 叠氮化合物 1 3-偶极环加成反应 三唑 低温固化 聚合体系 反应研究 炔丙基 双酚A 叠氮
在线阅读 下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部