Preparation of Co-MnOx/GAC catalyst by high-gravity technology and its mechanism for synergistic catalytic ozone degradation of phenol

IF 3.7 3区 工程技术 Q2 ENGINEERING, CHEMICAL
Cibin Wang , Kangrui Nie , Zhiwei Zhao , Yan Xue , Tong Zhao , Fuming Miao , Youzhi Liu , Weizhou Jiao
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引用次数: 0

Abstract

The impregnation method for preparing catalysts often faces challenges such as prolonged preparation times and poor dispersion of active components due to the limited mobility of the impregnation liquid. The rotating packed bed (RPB) can break the precursor solution into fine droplets, enabling dynamic impregnation of active components onto the surface of activated carbon. This approach facilitates the uniform distribution of active components on the carrier and enhances the stability and performance of the catalyst. In this study, activated carbon catalysts were prepared using high-gravity technology. It was found that the preparation time for Co-MnOx/GAC using the RPB method was reduced by 98%, the catalytic activity increased by 6.62%, and the loadings of active components increased by 13% and 17%, the catalytic activity remained stable after five cycles, with a significantly lower rate of metal dissolution. A suite of complementary analytical techniques demonstrates that Co-MnOx/GAC(RPB) has higher homogeneity and dispersion. X-ray photoelectron spectroscopy (XPS) results indicate that Co(II) and Mn(IV)/Mn(III) are the primary active sites during the catalytic decomposition of ozone, elucidating the mechanism of synergistic catalytic ozonation by dual-active components. Finally, electron paramagnetic resonance (EPR) confirmed that hydroxyl radicals (·OH) were the predominant reactive species in the reaction.
高重力技术制备Co-MnOx/GAC催化剂及其协同催化臭氧降解苯酚的机理
由于浸渍液的流动性有限,制备催化剂的浸渍方法常常面临制备时间长、活性组分分散差等挑战。旋转填充床(RPB)可以将前驱体溶液分解成细小的液滴,使活性成分动态浸渍在活性炭表面。这种方法有利于活性组分在载体上的均匀分布,提高了催化剂的稳定性和性能。本研究采用超重力法制备了活性炭催化剂。结果表明,采用RPB法制备Co-MnOx/GAC的时间缩短了98%,催化活性提高了6.62%,活性组分的负载分别提高了13%和17%,5个循环后催化活性保持稳定,金属溶解率明显降低。一套互补分析技术表明,Co-MnOx/GAC(RPB)具有较高的均匀性和分散性。x射线光电子能谱(XPS)结果表明,Co(II)和Mn(IV)/Mn(III)是臭氧催化分解过程中的主要活性位点,阐明了双活性组分协同催化臭氧化的机理。最后,电子顺磁共振(EPR)证实了在反应中羟基自由基(·OH)是主要的反应物质。
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来源期刊
Chinese Journal of Chemical Engineering
Chinese Journal of Chemical Engineering 工程技术-工程:化工
CiteScore
6.60
自引率
5.30%
发文量
4309
审稿时长
31 days
期刊介绍: The Chinese Journal of Chemical Engineering (Monthly, started in 1982) is the official journal of the Chemical Industry and Engineering Society of China and published by the Chemical Industry Press Co. Ltd. The aim of the journal is to develop the international exchange of scientific and technical information in the field of chemical engineering. It publishes original research papers that cover the major advancements and achievements in chemical engineering in China as well as some articles from overseas contributors. The topics of journal include chemical engineering, chemical technology, biochemical engineering, energy and environmental engineering and other relevant fields. Papers are published on the basis of their relevance to theoretical research, practical application or potential uses in the industry as Research Papers, Communications, Reviews and Perspectives. Prominent domestic and overseas chemical experts and scholars have been invited to form an International Advisory Board and the Editorial Committee. It enjoys recognition among Chinese academia and industry as a reliable source of information of what is going on in chemical engineering research, both domestic and abroad.
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