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UiO-66衍生的ZrOx负载的非晶态锰-铬催化剂上氯苯的催化氧化

Catalytic Oxidation of Chlorobenzene over Amorphous Manganese-Chromium Catalysts Supported by UiO-66-Derived ZrOx.

作者信息

Zhu Pengfei, Yuan Qiaosen, Li Na, Hu Zhaoxia, Chen Shouwen

机构信息

School of Biological and Environmental Engineering, Nanjing University of Science & Technology, Nanjing 210094, China.

出版信息

Materials (Basel). 2024 Apr 29;17(9):2103. doi: 10.3390/ma17092103.

Abstract

The development of efficient catalysts with longevity to remove chlorobenzene is challenging due to Cl poisoning. Herein, a series of Mn-Cr/ZrO catalysts supported by Zr-based metal-organic framework (UiO-66)-derived ZrO was prepared and investigated for chlorobenzene (CB) catalytic oxidation. MnCr/ZrO-M prepared via a wet impregnation method presented an amorphous structure, indicating the homogeneous dispersion of Cr and Mn, which improved acid and redox properties. 40Mn7Cr3/ZrO-M exhibited the best catalytic activity for chlorobenzene oxidation with T of 293 °C, which is mainly due to the strong interaction between manganese and chromium promoted by the large specific surface area of the ZrO support. Furthermore, 40Mn7Cr3/ZrO-M presented excellent stability for chlorobenzene oxidation.

摘要

由于氯中毒,开发具有长寿命的高效催化剂以去除氯苯具有挑战性。在此,制备了一系列由锆基金属有机框架(UiO-66)衍生的ZrO负载的Mn-Cr/ZrO催化剂,并对其进行氯苯(CB)催化氧化研究。通过湿浸渍法制备的MnCr/ZrO-M呈现非晶态结构,表明Cr和Mn均匀分散,这改善了酸性和氧化还原性能。40Mn7Cr3/ZrO-M对氯苯氧化表现出最佳催化活性,T为293℃,这主要归因于ZrO载体大比表面积促进的锰与铬之间的强相互作用。此外,40Mn7Cr3/ZrO-M对氯苯氧化表现出优异的稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c35/11084826/30697eb3fe83/materials-17-02103-g001.jpg

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