Mastering the Foreign Ionic Radius in CeO2 Supports of Ni-Based Catalysts for Efficient CO2 Methanation

IF 3.8 3区 工程技术 Q2 ENGINEERING, CHEMICAL Industrial & Engineering Chemistry Research Pub Date : 2024-09-28 DOI:10.1021/acs.iecr.4c02490
Hao Lou, Jie Ren, Nuo Xu, Inam Ullah, Syed Musab Ahmed, Zeeshan Abbasi, Wenlong Wu, Zhandong Wang
{"title":"Mastering the Foreign Ionic Radius in CeO2 Supports of Ni-Based Catalysts for Efficient CO2 Methanation","authors":"Hao Lou, Jie Ren, Nuo Xu, Inam Ullah, Syed Musab Ahmed, Zeeshan Abbasi, Wenlong Wu, Zhandong Wang","doi":"10.1021/acs.iecr.4c02490","DOIUrl":null,"url":null,"abstract":"A Ni-based catalyst is a common non-noble-metal system for CO<sub>2</sub> methanation, and metal modification for the support is an effective method to further improve its activity. Doping metals with various ionic radii already exhibited different effects on the methanation performance, but the promotion mechanism remains indistinct. Herein, we report a universal doping strategy to fabricate Ni-based catalysts by tailoring foreign ions (Al<sup>3+</sup>, Zr<sup>4+</sup>, Y<sup>3+</sup>, and Sm<sup>4+</sup>) with different radii in CeO<sub>2</sub>. Among them, Ni/Ce<sub>0.9</sub>Al<sub>0.1</sub>O<sub><i>x</i></sub> exhibited the highest catalytic performance (72.4% of CO<sub>2</sub> conversion at 300 °C) compared with other catalysts at all temperatures and with the lowest kinetic temperature range. Furthermore, the change in the foreign ionic radius had a variety of effects on the structure of the catalysts, in which the specific surface area and oxygen vacancy concentration were the main factors. According to mechanical measurements, the doping of foreign ions reduced the temperature of the started methanation and inhibited CO formation, resulting in enhanced catalytic activity CO<sub>2</sub> conversion and increased CH<sub>4</sub> selectivity. The hydroxyl groups derived from the oxygen vacancy facilitated the transformation of CO<sub>2</sub> to CH<sub>4</sub> via the HCOO* path. This work contributes to developing a promising approach to controlling the performance of CO<sub>2</sub> methanation by regulating the foreign ionic radius.","PeriodicalId":39,"journal":{"name":"Industrial & Engineering Chemistry Research","volume":null,"pages":null},"PeriodicalIF":3.8000,"publicationDate":"2024-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Industrial & Engineering Chemistry Research","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1021/acs.iecr.4c02490","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0

Abstract

A Ni-based catalyst is a common non-noble-metal system for CO2 methanation, and metal modification for the support is an effective method to further improve its activity. Doping metals with various ionic radii already exhibited different effects on the methanation performance, but the promotion mechanism remains indistinct. Herein, we report a universal doping strategy to fabricate Ni-based catalysts by tailoring foreign ions (Al3+, Zr4+, Y3+, and Sm4+) with different radii in CeO2. Among them, Ni/Ce0.9Al0.1Ox exhibited the highest catalytic performance (72.4% of CO2 conversion at 300 °C) compared with other catalysts at all temperatures and with the lowest kinetic temperature range. Furthermore, the change in the foreign ionic radius had a variety of effects on the structure of the catalysts, in which the specific surface area and oxygen vacancy concentration were the main factors. According to mechanical measurements, the doping of foreign ions reduced the temperature of the started methanation and inhibited CO formation, resulting in enhanced catalytic activity CO2 conversion and increased CH4 selectivity. The hydroxyl groups derived from the oxygen vacancy facilitated the transformation of CO2 to CH4 via the HCOO* path. This work contributes to developing a promising approach to controlling the performance of CO2 methanation by regulating the foreign ionic radius.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
掌握镍基催化剂 CeO2 载体中的外来离子半径以实现高效 CO2 甲烷化
镍基催化剂是一种常见的二氧化碳甲烷化非贵金属体系,而对载体进行金属改性是进一步提高其活性的有效方法。掺杂不同离子半径的金属已对甲烷化性能产生了不同的影响,但其促进机制仍不明确。在此,我们报告了一种通用的掺杂策略,通过在 CeO2 中定制不同半径的外来离子(Al3+、Zr4+、Y3+ 和 Sm4+)来制造 Ni 基催化剂。其中,与其他催化剂相比,Ni/Ce0.9Al0.1Ox 在所有温度下均表现出最高的催化性能(300 ℃ 时二氧化碳转化率为 72.4%),且动力学温度范围最低。此外,外来离子半径的变化对催化剂的结构产生了多种影响,其中比表面积和氧空位浓度是主要因素。根据力学测量,外来离子的掺杂降低了开始甲烷化的温度,抑制了 CO 的形成,从而提高了催化活性 CO2 转化率,增加了 CH4 选择性。氧空位产生的羟基促进了 CO2 通过 HCOO* 途径转化为 CH4。这项工作有助于开发出一种通过调节外来离子半径来控制 CO2 甲烷化性能的可行方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Industrial & Engineering Chemistry Research
Industrial & Engineering Chemistry Research 工程技术-工程:化工
CiteScore
7.40
自引率
7.10%
发文量
1467
审稿时长
2.8 months
期刊介绍: ndustrial & Engineering Chemistry, with variations in title and format, has been published since 1909 by the American Chemical Society. Industrial & Engineering Chemistry Research is a weekly publication that reports industrial and academic research in the broad fields of applied chemistry and chemical engineering with special focus on fundamentals, processes, and products.
期刊最新文献
Mastering the Foreign Ionic Radius in CeO2 Supports of Ni-Based Catalysts for Efficient CO2 Methanation Assessment of Nylon-6 Depolymerization for Circular Economy: Kinetic Modeling, Purification, Sustainable Process Design, and Industrial Practice NH3-SCR-DeNOx Activity of Cu-Containing Commercial Zeolite Y CoNi Alloy Modified Separators for High-Capacity and Long Cycle Lithium–Sulfur Batteries 2023 in Retrospective: Trends in Chemical Engineering
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1