IF 4.1 2区 化学 Q2 POLYMER SCIENCE
F. Pieringer, Y. Catel, R. Liska, P. Knaack
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引用次数: 0

摘要

许多聚合物材料(如粘合剂)的应用都需要在室温和环境气氛下进行聚合。在这种情况下,基于氧化还原引发的双组分(2K)体系因其可靠的性能而真正脱颖而出。在此,我们深入探讨了一种新开发的引发体系的聚合动力学,该体系基于铜催化二硼烷化合物的裂解,然后通过流变学与近红外进行耦合。通过对不同二硼烷的分析,我们进一步研究了二硼烷的浓度依赖性以及对凝胶时间的影响。此外,研究还表明,二硼烷/铜体系在高双键转化率下可产生高分子量的聚合物。此外,还介绍了二硼烷/铜引发自由基聚合的前景,因为各种不同类别的单体都表现出了极佳的聚合反应性,使这种引发体系在聚合物化学的各种应用中具有巨大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Insights into the bulk kinetics of a 2K radical polymerization system based on the copper catalyzed cleavage of diboranes and its perspectives

Insights into the bulk kinetics of a 2K radical polymerization system based on the copper catalyzed cleavage of diboranes and its perspectives
Many applications of polymer materials, such as adhesives, require a polymerization process at room temperature and ambient atmosphere. In those cases, two-component (2K) systems based on redox initiation truly stand out due to their reliable performance. Herein, we present a deep insight into the polymerization kinetics of a newly developed initiation system based on the copper catalyzed cleavage of diborane compounds, followed by rheology coupled with NIR. The analysis of different diboranes led us to further investigate the diborane concentration dependency and the effects on gel time that can be observed. Furthermore, it is shown that the diborane/Cu system yields polymers with high molecular weight at high double bond conversions. In addition, the perspectives of diborane/Cu initiation for radical polymerization are presented, as various different monomer classes showed excellent reactivity towards polymerization, enabling the great potential of this initiation system for various applications in polymer chemistry.
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来源期刊
Polymer Chemistry
Polymer Chemistry POLYMER SCIENCE-
CiteScore
8.60
自引率
8.70%
发文量
535
审稿时长
1.7 months
期刊介绍: Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.
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