Delayed Thiol-Epoxy Photopolymerization: A General and Effective Strategy to Prepare Thick Composites

被引:30
作者
Chen, Li [1 ,3 ]
Zheng, Yuanjian [1 ]
Meng, Xiaoyan [1 ,2 ]
Wei, Guo [1 ,3 ]
Dietliker, Kurt [2 ,4 ]
Li, Zhiquan [1 ,2 ]
机构
[1] Jiangnan Univ, Key Lab Synthet & Biol Colloids, Minist Educ, Sch Chem & Mat Engn, Wuxi 214122, Jiangsu, Peoples R China
[2] Jiangnan Univ, Int Res Ctr Photorespons Mol & Mat, Wuxi 214122, Jiangsu, Peoples R China
[3] Jiangsu Kailin Ruiyang Chem Co Ltd, Changzhou Radiat Curing Mat Engn Technol Res Ctr, Liyang 213364, Peoples R China
[4] Swiss Fed Inst Technol, Dept Chem & Appl Biosci, Lab Inorgan Chem, CH-8093 Zurich, Switzerland
关键词
POLYMERIZATION; BASE; PHOTOCATALYST; SYSTEMS; ACID;
D O I
10.1021/acsomega.0c01170
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photoinduced thiol-epoxy click polymerization possesses both the characteristics and advantages of photo-polymerization and click reactions. However, the photopolymerization of pigmented or highly filled thiol-epoxy thick composites still remains a great challenge due to the light screening effect derived from the competitive absorption, reflection, and scattering of the pigments or functional fillers. In this article, we present a simple and versatile strategy to prepare thick composites via delayed thiol-epoxy photopolymerization. The irradiation of a small area with a light-emitting diode (LED) point light source at room temperature leads to the decomposition of a photobase generator and the released active basic species can uniformly disperse throughout the whole system, including unirradiated areas, via mechanical stirring. No polymerization was observed at room temperature and therefore the liquid formulations can be further processed with molds of arbitrary size and desired shapes. It is only by increasing the temperature that base-catalyzed thiol-epoxy polymerization occurs and controllable preparation of thick thiol-epoxy materials can be achieved. The formed networks display excellent uniformity in different radii and depths with comparable functionality conversions, similar T-g values, and thermal decomposition temperatures. The presented strategy can be applied to prepare thick composites with glass fibers possessing improved mechanical properties and dark composites containing 2 wt % carbon nanotubes.
引用
收藏
页码:15192 / 15201
页数:10
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