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

IF 15.7 1区 化学 Q1 CHEMISTRY, APPLIED Chinese Journal of Catalysis Pub Date : 2024-11-01 DOI:10.1016/S1872-2067(24)60134-8
Zheng Li , Yuanyuan Dong , Ying Zeng , Mo Zhang , Hongjin Lv , Guo-Yu Yang
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Abstract

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.
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癸钨酸盐催化剂高选择性氧化对二甲苯至对苯二甲酸的连续流光催化系统
由于对苯二甲酸(TPA)的工业应用,对二甲苯(PX)选择性氧化为对苯二甲酸(TPA)越来越受到关注。然而,由于 PX 的 C(sp3)-H 键具有较高的键解离能,其氧化仍然是一个主要挑战。在此,研究人员使用癸钨酸四丁基铵(TBADT)光催化剂,以大气中的氧气为氧化剂,在 365 纳米 LED 光照射下,开发了一种将 PX 氧化为 TPA 的高效光催化系统。光催化 19 小时后,在 CH3CN(37.5% 1 mol L-1 HCl)溶剂中,通过简单的过滤处理,很容易从反应后溶液中分离出 TPA 产物,收率为 93.4%。由于 TPA 易于分离,且 TBADT 具有优异的回收稳定性,因此成功设计出了一种连续流光反应器,具有潜在的工业应用前景。机理研究阐明,盐酸添加剂的存在有利于[W10O32]4-阴离子结构的完整性以及激发态[W10O32]4-*向wO活性物种的转变,从而提高光氧化性能。
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来源期刊
Chinese Journal of Catalysis
Chinese Journal of Catalysis 工程技术-工程:化工
CiteScore
25.80
自引率
10.30%
发文量
235
审稿时长
1.2 months
期刊介绍: The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.
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