Lai Bo-Xin, Bhattacharjee Saurav, Huang Yi-Hao, Duh An-Bang, Wang Ping-Chieh, Tan Chung-Sung
Department of Chemical Engineering, National Tsing Hua University, No. 101, Section 2, Guangfu Road, East District, Hsinchu City 30013, Taiwan.
Chang Chun Plastics Co., Ltd., No.8, Zhonghua Road, Hsinchu Industrial Park, Hukou Township, Hsinchu County 30352, Taiwan.
Polymers (Basel). 2020 Oct 28;12(11):2513. doi: 10.3390/polym12112513.
A functional greener solvent mixture containing water, isopropyl alcohol (IPA) and ethyl acetate with the ratio 10:20:70 (wt%) was found to accelerate hydrogenation of bisphenol A type epoxy resin BE503 with a molecular weight of 1500 through an on-water mechanism, and led to an increased H availability, due to high solubility of H in IPA. Different carbon-based supports were tested and VulcanXC72 was found as the best support among the tested carbon-based ones as it possessed the highest amount of electron deficient promoter, RhO. The catalyst, Rh/VulcanXC72-polyol, synthesized by the microwave assisted polyol method, yielded a 100% hydrogenation of aromatic rings with an epoxy ring opening below 20.0% at 50 °C and a H pressure of 1000 psi in 2.25 h. Intrinsic activation energies for the hydrogenation of aromatic rings and epoxy ring opening were experimentally estimated and a mechanism for the hydrogenation of BE503 was proposed, wherein the hydrogenation of aromatic rings and epoxy ring opening in BE503 proceeded simultaneously in parallel and in-series with parallel being the major pathway.
一种由水、异丙醇(IPA)和乙酸乙酯按10:20:70(wt%)比例组成的功能性绿色溶剂混合物,通过水相机制加速了分子量为1500的双酚A型环氧树脂BE503的氢化反应,并且由于氢在IPA中的高溶解度,提高了氢的可利用性。测试了不同的碳基载体,发现VulcanXC72是测试的碳基载体中最佳的,因为它具有最高含量的缺电子促进剂RhO。通过微波辅助多元醇法合成的催化剂Rh/VulcanXC72-多元醇,在50℃和1000 psi氢气压力下,2.25小时内使芳香环的氢化率达到100%,环氧环开环率低于20.0%。通过实验估算了芳香环氢化和环氧环开环的本征活化能,并提出了BE503氢化反应的机理,其中BE503中芳香环的氢化和环氧环的开环同时以平行和串联方式进行,且平行方式是主要途径。