Selective synthesis of glyceryl monolaurate intensified by boric acid based deep eutectic solvent

被引:18
|
作者
Shen, Zilong [1 ]
Chen, Lifang [1 ]
Cheng, Hongye [1 ]
Qi, Zhiwen [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
Esterification; Lauric acid; Glycerol; Monolaurate; Deep eutectic solvents; COSMO; -RS; IONIC LIQUIDS; LAURIC ACID; FATTY-ACIDS; COSMO-RS; ESTERIFICATION KINETICS; CATALYTIC PERFORMANCE; CHOLINE CHLORIDE; BORONIC ACIDS; OXIDATION; OIL;
D O I
10.1016/j.cattod.2021.05.018
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Glyceryl monolaurate (GML), as one of widely used industrial chemicals, can be synthesized via Fischer ester-ification of lauric acid (LA) and glycerol (GL). In this work, we screened boric acid-based deep eutectic solvent (DES) formed from tetrapropylammonium bromide (TPAB) and boric acid to intensify the selective Fischer esterification through conductor-like screening model for realistic solvents (COSMO-RS) theory. The solid liquid equilibrium (SLE) phase behavior, hydrogen bond formation process, and thermal stability of the DES were characterized by differential scanning calorimetry (DSC), Fourier transform infrared spectrometry (FT-IR), and thermogravimetric analyzer (TGA). The results verified that equimolar TPAB and boric acid formed DES [TPAB:B (OH)3] with the lowest freezing point and very good thermal stability could efficiently intensify the Fischer esterification of GL and LA to GML. The hydrogen bond accepter TPAB of the DES made the esterification system homogeneous, which promoted the selective esterification process. In addition, the hydrogen bond donor B(OH)3 of the [TPAB:B(OH)3] combined with diol unit of GL to cyclic boric esters and led to a special selective space effect, which also improved the selectivity to GML. Thus, the esterification intensified of GL and LA by 20 wt% DES achieved GML selectivity of 85.7 % and yield of 76.4 % under the optimal reaction conditions. The ester-ification kinetics suggested the reaction followed pseudo-second-order model and the reaction activation energy was 33.98 kJ mol-1, similar to and/or lower than those reported works. Furthermore, DES and unreacted glycerol were readily recovered and reused through temperature controlled gravity-based separation due to the ability of homogeneity under reaction conditions and splitting phase behavior during the DES recovery. The results can expand the boric acid-based DESs for other potential intensification applications.
引用
收藏
页码:291 / 300
页数:10
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