Xiaohui Wang , Zhuang Li , Peng Zhao , Chao Yao , Jie Meng , Shixiang Zuo , Wei Zhu , Jingwei Liu , Fengqin Wu
{"title":"Construction of a catalyst using activated manganese ore and Co3O4 for efficient catalytic combustion of ethane†","authors":"Xiaohui Wang , Zhuang Li , Peng Zhao , Chao Yao , Jie Meng , Shixiang Zuo , Wei Zhu , Jingwei Liu , Fengqin Wu","doi":"10.1039/d4cy01224k","DOIUrl":null,"url":null,"abstract":"<div><div>Natural manganese ore (NMO) has received extensive attention on account of its inherent stability, abundant reserves, and low cost. The higher specific surface area and abundant active sites are considered crucial for catalytic combustion. However, owing to the limited specific surface area inherent to natural manganese ore, we employed an acid etching activation treatment to enlarge the specific surface area of NMO (from 17.8 m<sup>2</sup> g<sup>−1</sup> to 48.9 m<sup>2</sup> g<sup>−1</sup>). Herein, we successfully fabricated composite catalysts consisting of activated natural manganese ore (HNMO) and Co<sub>3</sub>O<sub>4</sub> using the ethylene glycol sol–gel method and then evaluated them for the catalytic combustion of ethane. Results showed that the catalytic performance of the composite catalysts for ethane could not be enhanced monotonically by increasing the introduction of Co indiscriminately. Among them, the Co<sub>2</sub>-HNMO catalyst exhibited a higher specific surface area, increased Mn<sup>4+</sup> and Co<sup>3+</sup> contents and higher oxygen mobility, which were attributed to the significant interaction between Co<sub>3</sub>O<sub>4</sub> and HNMO. The <em>T</em><sub>90</sub> of the corresponding Co<sub>2</sub>-HNMO catalyst was 294 °C under a space velocity of 40 000 mL g<sup>−1</sup> h<sup>−1</sup>. This work presents new insights into the design and synthesis of efficient composite catalysts based on natural minerals.</div></div>","PeriodicalId":66,"journal":{"name":"Catalysis Science & Technology","volume":"15 5","pages":"Pages 1664-1675"},"PeriodicalIF":4.2000,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Science & Technology","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2044475325000437","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Natural manganese ore (NMO) has received extensive attention on account of its inherent stability, abundant reserves, and low cost. The higher specific surface area and abundant active sites are considered crucial for catalytic combustion. However, owing to the limited specific surface area inherent to natural manganese ore, we employed an acid etching activation treatment to enlarge the specific surface area of NMO (from 17.8 m2 g−1 to 48.9 m2 g−1). Herein, we successfully fabricated composite catalysts consisting of activated natural manganese ore (HNMO) and Co3O4 using the ethylene glycol sol–gel method and then evaluated them for the catalytic combustion of ethane. Results showed that the catalytic performance of the composite catalysts for ethane could not be enhanced monotonically by increasing the introduction of Co indiscriminately. Among them, the Co2-HNMO catalyst exhibited a higher specific surface area, increased Mn4+ and Co3+ contents and higher oxygen mobility, which were attributed to the significant interaction between Co3O4 and HNMO. The T90 of the corresponding Co2-HNMO catalyst was 294 °C under a space velocity of 40 000 mL g−1 h−1. This work presents new insights into the design and synthesis of efficient composite catalysts based on natural minerals.
期刊介绍:
A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis.
Editor-in-chief: Bert Weckhuysen
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