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叔胺作为催化剂对苯并恶嗪开环聚合的影响。

The Effect of Tertiary Amines as Catalysts on the Ring-Opening Polymerization of Benzoxazines.

作者信息

Liu Fanghui, Wu Ximeng, Chen Kun, Yao Junbo, Ran Qichao

机构信息

Sinopec Key Laboratory of Drilling Completion and Fracturing of Shale Oil and Gas, Beijing 102206, China.

College of Polymer Science and Engineering, Sichuan University, Chengdu 610065, China.

出版信息

Polymers (Basel). 2025 May 22;17(11):1431. doi: 10.3390/polym17111431.

Abstract

Benzoxazines are a kind of high-performance thermosetting resin that can undergo ring-opening polymerization to generate cross-linking structures. Here, two benzoxazine monomers, bisphenol A/aniline type (BA-a) and bisphenol A/tert-butylamine type (BA-tb), were synthesized and mixed with three tertiary amine catalysts like 2-methylimidazole (2MI), 1,2-dimethylimidazole (12MI), 4-dimethylaminopyridine (DMAP). Differential scanning calorimetry (DSC) was performed to study the curing behaviors and the curing kinetics of two benzoxazine/catalyst systems. The results indicated that all amines had a catalytic effect on the polymerization of both benzoxazines, and the BA-a/catalyst systems showed relatively higher activity. In addition, Fourier transform infrared (FTIR) and nuclear magnetic resonance (NMR) spectra were procured to analyze structural changes in the benzoxazine/catalyst systems during the curing process. The presence of the catalysts promoted the progress of the ring-opening reactions and the formation of the phenolic units in the cross-linking structures, and these evolutions were more obvious for the BA-a/catalyst system than the BA-tb/catalyst system. Furthermore, a thermogravimetric analysis (TGA) was conducted to analyze the thermal stability of the cured systems. Finally, possible curing reaction mechanisms were proposed for these benzoxazine/amine systems.

摘要

苯并恶嗪是一种高性能热固性树脂,可通过开环聚合生成交联结构。在此,合成了两种苯并恶嗪单体,双酚A/苯胺型(BA-a)和双酚A/叔丁胺型(BA-tb),并将它们与三种叔胺催化剂如2-甲基咪唑(2MI)、1,2-二甲基咪唑(12MI)、4-二甲基氨基吡啶(DMAP)混合。采用差示扫描量热法(DSC)研究了两种苯并恶嗪/催化剂体系的固化行为和固化动力学。结果表明,所有胺类对两种苯并恶嗪的聚合均有催化作用,且BA-a/催化剂体系表现出相对较高的活性。此外,还获得了傅里叶变换红外光谱(FTIR)和核磁共振光谱(NMR),以分析苯并恶嗪/催化剂体系在固化过程中的结构变化。催化剂的存在促进了开环反应的进行以及交联结构中酚单元的形成,并且这些变化在BA-a/催化剂体系中比在BA-tb/催化剂体系中更为明显。此外,进行了热重分析(TGA)以分析固化体系的热稳定性。最后,提出了这些苯并恶嗪/胺体系可能的固化反应机理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d718/12157157/3bc4df3cd337/polymers-17-01431-g001.jpg

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