Zheng Li , Yuanyuan Dong , Ying Zeng , Mo Zhang , Hongjin Lv , Guo-Yu Yang
{"title":"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","authors":"Zheng Li , Yuanyuan Dong , Ying Zeng , Mo Zhang , Hongjin Lv , Guo-Yu Yang","doi":"10.1016/S1872-2067(24)60134-8","DOIUrl":null,"url":null,"abstract":"<div><div>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(<em>sp</em><sup>3</sup>)‒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 CH<sub>3</sub>CN (37.5% 1 mol L<sup>−1</sup> 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 [W<sub>10</sub>O<sub>32</sub>]<sup>4−</sup> anions and the transition from excited states [W<sub>10</sub>O<sub>32</sub>]<sup>4−</sup>* to wO active species, leading to enhanced photooxidation performance.</div></div>","PeriodicalId":9832,"journal":{"name":"Chinese Journal of Catalysis","volume":"66 ","pages":"Pages 282-291"},"PeriodicalIF":15.7000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A continuous-flow photocatalytic system for highly selective oxidation of p-xylene to terephthalic acid by decatungstate catalyst\",\"authors\":\"Zheng Li , Yuanyuan Dong , Ying Zeng , Mo Zhang , Hongjin Lv , Guo-Yu Yang\",\"doi\":\"10.1016/S1872-2067(24)60134-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>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(<em>sp</em><sup>3</sup>)‒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 CH<sub>3</sub>CN (37.5% 1 mol L<sup>−1</sup> 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 [W<sub>10</sub>O<sub>32</sub>]<sup>4−</sup> anions and the transition from excited states [W<sub>10</sub>O<sub>32</sub>]<sup>4−</sup>* to wO active species, leading to enhanced photooxidation performance.</div></div>\",\"PeriodicalId\":9832,\"journal\":{\"name\":\"Chinese Journal of Catalysis\",\"volume\":\"66 \",\"pages\":\"Pages 282-291\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2024-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Journal of Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1872206724601348\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1872206724601348","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
A continuous-flow photocatalytic system for highly selective oxidation of p-xylene to terephthalic acid by decatungstate catalyst
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.
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.