Role of MgAl2O4 and γ-Al2O3 Supports in Modulating Oxygen Activity of LaFeO3 for Methane Oxidation

IF 2.3 4区 化学 Q3 CHEMISTRY, PHYSICAL
Minsu Park, Hyemin An, Siwon Lee
{"title":"Role of MgAl2O4 and γ-Al2O3 Supports in Modulating Oxygen Activity of LaFeO3 for Methane Oxidation","authors":"Minsu Park,&nbsp;Hyemin An,&nbsp;Siwon Lee","doi":"10.1007/s10562-025-05091-9","DOIUrl":null,"url":null,"abstract":"<div><p>Developing advanced methane conversion catalysts is essential for reducing methane emissions and enhancing gas turbine performance. In this study, LaFeO<sub>3</sub> perovskite catalysts supported on high-surface-area γ-Al<sub>2</sub>O<sub>3</sub> and MgAl<sub>2</sub>O<sub>4</sub> were synthesized via the sol-gel method and evaluated for methane oxidation. Structural and compositional analyses confirmed the successful incorporation of LaFeO<sub>3</sub> on MgAl<sub>2</sub>O<sub>4</sub>, whereas its formation on γ-Al<sub>2</sub>O<sub>3</sub> was limited by interactions with underlying support, leading to secondary phase formation. Quantitative modeling based on rate equations revealed the contributions of two oxygen species (i.e., surface oxygen and lattice oxygen) to the reaction, elucidating catalyst-specific reaction pathways. The MgAl<sub>2</sub>O<sub>4</sub>-supported LaFeO<sub>3</sub> exhibited enhanced methane oxidation performance compared to conventional LaFeO<sub>3</sub> due to the increased participation of both lattice and surface oxygen species in the reaction. In contrast, the γ-Al<sub>2</sub>O<sub>3</sub>-supported LaFeO<sub>3</sub> catalyst performed similarly to bulk LaFeO<sub>3</sub>, likely due to Al-induced secondary phases that suppressed oxygen availability. These findings offer novel insights into optimizing methane oxidation catalysts through rational material design.</p><h3>Graphical Abstract</h3><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":508,"journal":{"name":"Catalysis Letters","volume":"155 8","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Letters","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10562-025-05091-9","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Developing advanced methane conversion catalysts is essential for reducing methane emissions and enhancing gas turbine performance. In this study, LaFeO3 perovskite catalysts supported on high-surface-area γ-Al2O3 and MgAl2O4 were synthesized via the sol-gel method and evaluated for methane oxidation. Structural and compositional analyses confirmed the successful incorporation of LaFeO3 on MgAl2O4, whereas its formation on γ-Al2O3 was limited by interactions with underlying support, leading to secondary phase formation. Quantitative modeling based on rate equations revealed the contributions of two oxygen species (i.e., surface oxygen and lattice oxygen) to the reaction, elucidating catalyst-specific reaction pathways. The MgAl2O4-supported LaFeO3 exhibited enhanced methane oxidation performance compared to conventional LaFeO3 due to the increased participation of both lattice and surface oxygen species in the reaction. In contrast, the γ-Al2O3-supported LaFeO3 catalyst performed similarly to bulk LaFeO3, likely due to Al-induced secondary phases that suppressed oxygen availability. These findings offer novel insights into optimizing methane oxidation catalysts through rational material design.

Graphical Abstract

MgAl2O4和γ-Al2O3载体在调节LaFeO3氧化甲烷氧活性中的作用
开发先进的甲烷转化催化剂对于减少甲烷排放和提高燃气轮机性能至关重要。本研究采用溶胶-凝胶法合成了高表面积γ-Al2O3和MgAl2O4负载的LaFeO3钙钛矿催化剂,并对其甲烷氧化性能进行了评价。结构和成分分析证实了LaFeO3在MgAl2O4上的成功结合,而其在γ-Al2O3上的形成受到了与底层支撑物相互作用的限制,导致了二次相的形成。基于速率方程的定量建模揭示了两种氧(即表面氧和晶格氧)对反应的贡献,阐明了催化剂特异性反应途径。与传统的LaFeO3相比,mgal2o4负载的LaFeO3表现出更强的甲烷氧化性能,这是由于在反应中增加了晶格和表面氧的参与。相比之下,γ- al2o3负载的LaFeO3催化剂的性能与本体LaFeO3相似,可能是由于al诱导的二次相抑制了氧的可用性。这些发现为通过合理的材料设计优化甲烷氧化催化剂提供了新的见解。图形抽象
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 求助全文
来源期刊
Catalysis Letters
Catalysis Letters 化学-物理化学
CiteScore
5.70
自引率
3.60%
发文量
327
审稿时长
1 months
期刊介绍: Catalysis Letters aim is the rapid publication of outstanding and high-impact original research articles in catalysis. The scope of the journal covers a broad range of topics in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis. The high-quality original research articles published in Catalysis Letters are subject to rigorous peer review. Accepted papers are published online first and subsequently in print issues. All contributions must include a graphical abstract. Manuscripts should be written in English and the responsibility lies with the authors to ensure that they are grammatically and linguistically correct. Authors for whom English is not the working language are encouraged to consider using a professional language-editing service before submitting their manuscripts.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信