Promoting distribution of surface-active sites by regulates interfacial binding of TiO2 and Pt using organic acid: stable Cl-VOCs catalytic properties

IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2025-04-05 DOI:10.1016/j.mcat.2025.115077
Esimoneze Emmanuel Chinedu , Dilong Qiang , Xueqian Wu , Wei Liu , Haizhou Cao , Zhaolian Ye , Zhen Li , Songjian Zhao
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Abstract

The Pt-based catalyst for purifying chlorinated volatile organic compounds (Cl-VOCs) has the advantages of high catalytic efficiency and low ignition temperature, but the problem of poor resistance to chlorine and water poisoning has not been effectively solved. A series of 0.5 Pt-Ti catalysts were prepared for chlorobenzene (CB) catalytic oxidation by adjusting the interfacial stability and dispersibility of the TiO2 and Pt through the organic acid strategy in this study. The introduction of tartaric acid (TA) effectively enhanced the surface reduction performance of 0.5Pt-Ti-TA and the proportion of Pt4+ on the surface. In addition, TA can strongly coordinate with Ti center to form stable titanium-containing complexes, improve the dispersion of Pt, prevent particles from agglomerating, and make the distribution of active sites more uniform. The designed 0.5Pt-Ti-TA exhibits excellent chlorine and water resistance at 300℃ (5 %H2O, 500 ppm CB), and has a higher potential of application.

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利用有机酸调节TiO2和Pt的界面结合,促进表面活性位点的分布:稳定的Cl-VOCs催化性能
用于净化氯化挥发性有机化合物(Cl-VOCs)的铂基催化剂具有催化效率高、着火温度低等优点,但其抗氯气和水毒性差的问题一直未得到有效解决。本研究通过有机酸策略调节 TiO2 和 Pt 的界面稳定性和分散性,制备了一系列 0.5 Pt-Ti 催化剂,用于氯苯(CB)催化氧化。酒石酸(TA)的引入有效提高了 0.5Pt-Ti-TA 的表面还原性能和表面 Pt4+ 的比例。此外,TA 能与 Ti 中心强配位,形成稳定的含钛络合物,改善铂的分散性,防止颗粒团聚,使活性位点分布更均匀。所设计的 0.5Pt-Ti-TA 在 300℃(5%H2O,500 ppm CB)条件下表现出优异的耐氯性和耐水性,具有更高的应用潜力。
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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