光引发剂
材料科学
碳纤维
纳米技术
聚合物
复合材料
复合数
单体
作者
Ruiping Li,Hongda Guo,Xiongfei Luo,Qunying Wang,Yulian Pang,Shujun Li,Shouxin Liu,Jian Li,Bernd Strehmel,Zhijun Chen
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-04-29
卷期号:63 (29): e202404454-e202404454
被引量:17
标识
DOI:10.1002/anie.202404454
摘要
Sustainable carbon dots comprising surficial oxime ester groups following homolytic bond cleavage exhibit potential as photoinitiators for traditional free radical photopolymerization. Carbon dots were made following a solvothermal procedure from sustainable furfural available from lignocellulose. Surficial aldehyde moieties reacted with hydroxylamine to the respective oxime while reaction with benzoyl chloride resulted in a biobased Type I photoinitiator comprising sustainable carbon dot (CD-PI). Photoinitiating ability was compared with the traditional photoinitiator (PI) ethyl (2,4,6-trimethyl benzoyl) phenyl phosphinate (TPO-L) by real-time FTIR with UV exposure at 365 nm. Photopolymer composition based on a mixture of urethane dimethacrylate (UDMA) and tripropylene glycol diacrylate (TPGDA) resulted in a similar final conversion of about 70 % using either CD-PI or TPO-L. Nevertheless, it appeared homogeneous in the case of compositions processed with CD-PI, while those made with TPO-L were heterogeneous as shown by two glass transition temperatures. Moreover, the migration rate of CD-PI in the cured samples was lower in comparison with those samples using TPO-L as PI.
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