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改性纳米纤维素/单体浇铸尼龙复合材料的结晶动力学

Crystallization Kinetics of Modified Nanocellulose/Monomer Casting Nylon Composites.

作者信息

He Xiaofeng, Guo Fuqiang, Tang Kaihong, Ge Tiejun

机构信息

Department of Polymer Science and Engineering, Shenyang University of Chemical Technology, Shenyang 110142, China.

Liaoning Polymer Materials Engineering and Technology Research Center, Shenyang 110142, China.

出版信息

Polymers (Basel). 2023 Jan 31;15(3):719. doi: 10.3390/polym15030719.

Abstract

Polyisocyanate and caprolactone were used to chemically functionalize nanocellulose (CNF). Composites of CNF, caprolactone-modified nanocellulose (CNF-CL) and polyisocyanate-modified nanocellulose (CNF-JQ)/MC nylon were fabricated by anionic ring-opening polymerization. The effects of the crystal structure, crystal morphology and crystallization process of MC nylon composites have been characterized by wide-angle X-ray diffraction (WAXD), polarized optical microscopy(POM) and differential scanning calorimetry (DSC). Isothermal crystallization kinetics were analyzed using the Avrami equation, and the crystallization rate, half-time, and Avrami exponent were calculated. The results show that the nucleation effects of CNF-JQ/MC nylon composites is increased with the CNF-JQ increase, and it is best compared with MC nylon, CNF/MC nylon and CNF-CL/MC nylon composites, so CNF-JQ can play the role of effective nucleating agent in MC nylon. We also discussed the non-isothermal crystallization of the composites. Analysis of the Jeziorny and Mo model demonstrates that the Zc values of CNF, CNF-CL, CNF-JQ/MC nylon composites increase, and the F(T) values decrease in order. This indicates that CNF-JQ can better promote the crystallization rate of non-isothermal crystallization of MC nylon. The results of this work demonstrate that CNF-JQ can be an effective nucleation agent and increase the crystallization rate of MC nylon compared with CNF-CL. The activation energy of the composites was studied using the kissing method, and the results showed that CNF-CL decreased the activation energy of MC nylon, and CNF and CNF-JQ increased the activation energy of MC nylon.

摘要

采用多异氰酸酯和己内酯对纳米纤维素(CNF)进行化学功能化处理。通过阴离子开环聚合制备了CNF、己内酯改性纳米纤维素(CNF-CL)和多异氰酸酯改性纳米纤维素(CNF-JQ)/MC尼龙复合材料。利用广角X射线衍射(WAXD)、偏光显微镜(POM)和差示扫描量热法(DSC)对MC尼龙复合材料的晶体结构、晶体形态和结晶过程进行了表征。使用Avrami方程分析等温结晶动力学,并计算结晶速率、半衰期和Avrami指数。结果表明,随着CNF-JQ含量的增加,CNF-JQ/MC尼龙复合材料的成核效果增强,与MC尼龙、CNF/MC尼龙和CNF-CL/MC尼龙复合材料相比效果最佳,因此CNF-JQ在MC尼龙中可起到有效成核剂的作用。我们还讨论了复合材料的非等温结晶。对Jeziorny和Mo模型的分析表明,CNF、CNF-CL、CNF-JQ/MC尼龙复合材料的Zc值增大,F(T)值依次减小。这表明CNF-JQ能更好地促进MC尼龙非等温结晶的速率。这项工作的结果表明,与CNF-CL相比,CNF-JQ可作为有效的成核剂并提高MC尼龙的结晶速率。采用“接吻法”研究了复合材料的活化能,结果表明CNF-CL降低了MC尼龙的活化能,而CNF和CNF-JQ提高了MC尼龙的活化能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821a/9920481/a97d0c1144f5/polymers-15-00719-g001.jpg

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