New insights into improved SO2＆H2O resistance over MoCrCeOx catalyst by CTAB for medium-low temperatures NH3-SCR: Regulation of surface acid and oxygen species

IF 5.6 2区工程技术 Q2 ENERGY & FUELS Journal of The Energy Institute Pub Date : 2024-08-15 DOI:10.1016/j.joei.2024.101793

Junge Yun , Hanbing Zhang , Xiaomei Hu , Cheng Zhao , Ninghan Wei , Xueying Jiang , Zhangfa Tong , Zhihang Chen

{"title":"New insights into improved SO2＆H2O resistance over MoCrCeOx catalyst by CTAB for medium-low temperatures NH3-SCR: Regulation of surface acid and oxygen species","authors":"Junge Yun , Hanbing Zhang , Xiaomei Hu , Cheng Zhao , Ninghan Wei , Xueying Jiang , Zhangfa Tong , Zhihang Chen","doi":"10.1016/j.joei.2024.101793","DOIUrl":null,"url":null,"abstract":"<div><div>Selective catalytic reduction (NH3-SCR) of NH3 is the most efficient NOx removal technology. Improving the SO2/H2O resistance of SCR catalyst is of great importance for its industrial application. The Mo(0.3)-CrCeOx catalysts synthesized by the citric acid method exhibited excellent high concentration SO2 resistance but poor H2O tolerance. In this work, cetyltrimethylammonium bromide (CTAB) was used to improve SO2＆H2O resistance over Mo(0.3)-CrCeOx catalyst at medium-low temperatures. The mechanism of CTAB modification and the discrepancy to citric acid (CA) method were investigated. The results indicated that the CTAB catalyst had a large specific surface area, and was conducive to forming a specific structural strength. The enhancement of surface acidity of CTAB is the reason for the further enhancement of SCR activity. The regulation of hydroxyl oxygen to promote the activation of Brønsted acid sites is the key factor to SO2＆H2O resistance. In addition, the in-situ DRIFTS results revealed the different mechanisms of the two catalysts. This paper raised the deactivation reason of sol-gel catalyst caused by SO2＆H2O and presented an effective modification strategy.</div></div>","PeriodicalId":17287,"journal":{"name":"Journal of The Energy Institute","volume":"118 ","pages":"Article 101793"},"PeriodicalIF":5.6000,"publicationDate":"2024-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Energy Institute","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S174396712400271X","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}

引用次数: 0

Abstract

Selective catalytic reduction (NH₃-SCR) of NH₃ is the most efficient NO_x removal technology. Improving the SO₂/H₂O resistance of SCR catalyst is of great importance for its industrial application. The Mo(0.3)-CrCeO_x catalysts synthesized by the citric acid method exhibited excellent high concentration SO₂ resistance but poor H₂O tolerance. In this work, cetyltrimethylammonium bromide (CTAB) was used to improve SO₂＆H₂O resistance over Mo(0.3)-CrCeO_x catalyst at medium-low temperatures. The mechanism of CTAB modification and the discrepancy to citric acid (CA) method were investigated. The results indicated that the CTAB catalyst had a large specific surface area, and was conducive to forming a specific structural strength. The enhancement of surface acidity of CTAB is the reason for the further enhancement of SCR activity. The regulation of hydroxyl oxygen to promote the activation of Brønsted acid sites is the key factor to SO₂＆H₂O resistance. In addition, the in-situ DRIFTS results revealed the different mechanisms of the two catalysts. This paper raised the deactivation reason of sol-gel catalyst caused by SO₂＆H₂O and presented an effective modification strategy.

Abstract Image

查看原文

微信好友朋友圈 QQ好友复制链接

本刊更多论文

中低温 NH3-SCR 用 CTAB 改善 MoCrCeOx 催化剂抗 SO2&H2O 性能的新见解：表面酸和氧物种的调控

氮氧化物的选择性催化还原（NH3-SCR）是最有效的氮氧化物去除技术。提高 SCR 催化剂的抗 SO2/H2O 性能对其工业应用具有重要意义。用柠檬酸法合成的 Mo(0.3)-CrCeOx 催化剂具有优异的耐高浓度 SO2 性能，但耐 H2O 性能较差。本研究采用十六烷基三甲基溴化铵（CTAB）改善了 Mo(0.3)-CrCeOx 催化剂在中低温下的耐 SO2&H2O 性能。研究了 CTAB 改性的机理以及与柠檬酸（CA）法的差异。结果表明，CTAB 催化剂具有较大的比表面积，有利于形成特定的结构强度。CTAB 表面酸性的增强是进一步提高 SCR 活性的原因。调节羟基氧以促进布氏酸位点的活化是抗 SO2＆H2O 的关键因素。此外，原位 DRIFTS 结果还揭示了两种催化剂的不同机理。本文提出了溶胶-凝胶催化剂因 SO2＆H2O 而失活的原因，并提出了有效的改性策略。

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

Journal of The Energy Institute 工程技术-能源与燃料

CiteScore

10.60

自引率

5.30%

发文量

166

审稿时长

16 days

期刊介绍： The Journal of the Energy Institute provides peer reviewed coverage of original high quality research on energy, engineering and technology.The coverage is broad and the main areas of interest include: Combustion engineering and associated technologies; process heating; power generation; engines and propulsion; emissions and environmental pollution control; clean coal technologies; carbon abatement technologies Emissions and environmental pollution control; safety and hazards; Clean coal technologies; carbon abatement technologies, including carbon capture and storage, CCS; Petroleum engineering and fuel quality, including storage and transport Alternative energy sources; biomass utilisation and biomass conversion technologies; energy from waste, incineration and recycling Energy conversion, energy recovery and energy efficiency; space heating, fuel cells, heat pumps and cooling systems Energy storage The journal''s coverage reflects changes in energy technology that result from the transition to more efficient energy production and end use together with reduced carbon emission.