Degradation of polycarbonate to produce bisphenol A catalyzed by imidazolium-based DESs under metal-and solvent-free conditions

被引:25
作者
Huang, Wenwen [1 ]
Wang, Hui [2 ]
Hu, Weiyue [1 ]
Yang, Daoshan [1 ]
Yu, Shitao [3 ]
Liu, Fusheng [3 ]
Song, Xiuyan [1 ]
机构
[1] Qingdao Univ Sci & Technol, State Key Lab Base Ecochem Engn, Coll Chem & Mol Engn, Qingdao 266042, Peoples R China
[2] Qingdao Agr Univ, Coll Chem & Pharmaceut Sci, Qingdao 266109, Peoples R China
[3] Qingdao Univ Sci & Technol, Coll Chem Engn, Qingdao 266042, Peoples R China
基金
中国国家自然科学基金;
关键词
DEEP-EUTECTIC SOLVENTS; IONIC LIQUIDS; POLYETHYLENE TEREPHTHALATE; ALKALINE-HYDROLYSIS; ALCOHOLYSIS; WASTES; POLY(BISPHENOL; CARBONATE); EXTRACTION; POLYMERS;
D O I
10.1039/d0ra09215k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bisphenol A (BPA) is an important chemical raw material, but the traditional preparation process of BPA is costly and complicated, so it is necessary to find an efficient and environmentally friendly method for the production of BPA. Deep eutectic solvents (DESs) have attracted widespread attention due to their low cost, low toxicity, low melting point, non-volatilization, easy preparation, recyclablility and biodegradability. In this work, a series of imidazolium-based DESs were synthesized and used for the degradation of polycarbonate (PC), and BPA was obtained from the methanolysis of PC catalyzed by DESs under metal- and solvent-free conditions. It was found that imidazolium-based DES [EmimOH]Cl-2Urea showed excellent catalytic activity and reusability. Under the optimized reaction conditions (the mass ratio of DES to PC is 0.1 : 1, the molar ratio of CH3OH to PC is 5 : 1, 120 degrees C, reaction time 2 h), the PC conversion and BPA yield were almost 100% and 98%, respectively. Moreover, the kinetics of methanolysis catalyzed by [EmimOH]Cl-2Urea was investigated in the temperature range 100-120 degrees C, and the results indicated that it is a pseudo-first order reaction with an activation energy of 133.59 kJ mol(-1). In addition, a possible catalytic mechanism of PC methanolysis is proposed.
引用
收藏
页码:1595 / 1604
页数:10
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