A continuous-flow photocatalytic system for highly selective oxidation of p-xylene to terephthalic acid by decatungstate catalyst

被引:0
|
作者
Li, Zheng [1 ]
Dong, Yuanyuan [1 ]
Zeng, Ying [1 ]
Zhang, Mo [1 ]
Lv, Hongjin [1 ,2 ]
Yang, Guo-Yu [1 ]
机构
[1] Beijing Inst Technol, Sch Chem & Chem Engn, MOE Key Lab Cluster Sci, Beijing Key Lab Photoelect Electrophoton Convers M, Beijing 102488, Peoples R China
[2] Beijing Inst Technol, Tangshan Res Inst, Tangshan 063000, Hebei, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Photocatalysis; Decatungstate; Aerobic oxidation; Continuous-flow catalysis; Self-separation of product; MOLECULAR-OXYGEN; WATER; CYCLOHEXANE; ANION; STATE; REACTIVITY; CONVERSION; ARYLATION; HAT;
D O I
10.1016/S1872-2067(24)60134-8
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The selective oxidation of para-xylene (PX) to terephthalic acid (TPA) has received increasing attention due to the industrial applications of TPA. However, the oxidation of the C(sp3)-H bond of PX is still a main challenge because of the higher bond dissociation energy. Herein, an efficient photocatalytic system for the oxidation of PX to TPA was developed by using tetrabutylammonium decatungstate (TBADT) photocatalyst using atmospheric oxygen as oxidant and 365 nm LED light irradiation. The resulting TPA product was easily separated from the post-reaction solution through simple filtration treatment with a 93.4% yield in CH3CN (37.5% 1 mol L-1 HCl) solvent after 19-h photocatalysis. Given the easy separation of TPA and the excellent recycling stability of TBADT, a continuous-flow photoreactor was successfully designed with promising prospect for potential industrial application. Mechanistic studies elucidated that the presence of HCl additive benefits the structural integrity of [W10O32]4- anions and the transition from excited states [W10O32]4-* to wO active species, leading to enhanced photooxidation performance. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:282 / 291
页数:10
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