Chemo-enzymatic phenol polymerisation via in-situ H2O2 synthesis

IF 5.3 2区 化学 Q1 CHEMISTRY, APPLIED Catalysis Today Pub Date : 2025-06-15 Epub Date: 2025-03-24 DOI:10.1016/j.cattod.2025.115292
Liwei Zhang , Richard J. Lewis , Joseph Brehm , Wencong Liu , David J. Morgan , Thomas E. Davies , Yong Wang , Graham J. Hutchings
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Abstract

Within this contribution, the combination of supported AuPd nanoalloys with horseradish peroxidase is demonstrated to offer high efficacy towards the one-pot oxidative polymerisation of the model wastewater contaminant phenol, via the chemo-catalytic supply of in-situ generated H2O2. Notably, the utilisation of AuPd alloyed formulations offered considerably improved cascade efficiencies, compared to that observed over monometallic analogues, with the optimal 0.5%Au-0.5%Pd/TiO2 catalyst achieving total conversion of phenol within 15 minutes when used in conjunction with the enzyme. Importantly, the in-situ chemo-enzymatic system was shown to offer good stability over successive reactions, and outperforms analogous approaches reliant on the use of preformed H2O2, while also avoiding the proprietary stabilising agents present in the commercial oxidant.
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原位H2O2合成化学酶催化苯酚聚合
在这项贡献中,负载型AuPd纳米合金与辣根过氧化物酶的组合被证明可以通过原位生成H2O2的化学催化供应,对模型废水污染物苯酚的一锅氧化聚合提供高效率。值得注意的是,与单金属类似物相比,使用AuPd合金配方可以显著提高级联效率,当与酶结合使用时,最佳的0.5%Au-0.5%Pd/TiO2催化剂可以在15分钟内实现苯酚的完全转化。重要的是,原位化学酶系统在连续反应中具有良好的稳定性,并且优于依赖于使用预成型H2O2的类似方法,同时也避免了商用氧化剂中存在的专有稳定剂。
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来源期刊
Catalysis Today
Catalysis Today 化学-工程:化工
CiteScore
11.50
自引率
3.80%
发文量
573
审稿时长
2.9 months
期刊介绍: Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues. Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.
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