Superior catalytic combustion of methane over Pd supported on oxygen vacancy-rich NiAl2O4

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL Catalysis Science & Technology Pub Date : 2024-08-26 DOI:10.1039/d4cy00620h
Sha Li, Jie Li, Zirui He, Yao Sheng, Wen Liu
{"title":"Superior catalytic combustion of methane over Pd supported on oxygen vacancy-rich NiAl2O4","authors":"Sha Li, Jie Li, Zirui He, Yao Sheng, Wen Liu","doi":"10.1039/d4cy00620h","DOIUrl":null,"url":null,"abstract":"Catalytic combustion of methane is an effective solution to reducing the greenhouse gas emission from natural gas-fueled engines. However, existing methane combustion catalysts suffer from insufficient low-temperature activity and poor hydrothermal stability. In this study, we demonstrate that PdO nanoparticles supported on oxygen vacancy-rich NiAl<small><sub>2</sub></small>O<small><sub>4</sub></small> spinel, prepared by a simple and affordable procedure, render a remarkable enhancement in catalytic methane combustion below 400 °C. The calcination temperature was used as a robust means to tune the concentration of oxygen vacancies in the NiAl<small><sub>2</sub></small>O<small><sub>4</sub></small> spinel. The particle size of PdO can be effectively controlled by adjusting the temperature of the subsequent calcination of the Pd-loaded spinel catalyst. The optimized catalyst, Pd/NiAl<small><sub>2</sub></small>O<small><sub>4</sub></small>-900–550, <em>i.e.</em> NiAl<small><sub>2</sub></small>O<small><sub>4</sub></small> calcined at 900 °C, impregnated with Pd, and subsequently calcined at 550 °C, achieved a <em>T</em><small><sub>50</sub></small> as low as 325 °C, whilst exhibiting excellent stability. After continuous treatment in 10% H<small><sub>2</sub></small>O at 750 °C for 10 h, <em>T</em><small><sub>50</sub></small> remains at below 396 °C. The characterization of the catalyst before, after and <em>in situ</em> methane combustion confirms that the high oxygen vacancy concentration and stable PdO nanoparticles both contribute to its excellent activity and stability. The present study introduces a new paradigm for preparing cost-effective and scalable redox catalysts supported on NiAl<small><sub>2</sub></small>O<small><sub>4</sub></small> spinel with rich and tunable oxygen vacancies.","PeriodicalId":66,"journal":{"name":"Catalysis Science & Technology","volume":null,"pages":null},"PeriodicalIF":4.4000,"publicationDate":"2024-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Science & Technology","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4cy00620h","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

Catalytic combustion of methane is an effective solution to reducing the greenhouse gas emission from natural gas-fueled engines. However, existing methane combustion catalysts suffer from insufficient low-temperature activity and poor hydrothermal stability. In this study, we demonstrate that PdO nanoparticles supported on oxygen vacancy-rich NiAl2O4 spinel, prepared by a simple and affordable procedure, render a remarkable enhancement in catalytic methane combustion below 400 °C. The calcination temperature was used as a robust means to tune the concentration of oxygen vacancies in the NiAl2O4 spinel. The particle size of PdO can be effectively controlled by adjusting the temperature of the subsequent calcination of the Pd-loaded spinel catalyst. The optimized catalyst, Pd/NiAl2O4-900–550, i.e. NiAl2O4 calcined at 900 °C, impregnated with Pd, and subsequently calcined at 550 °C, achieved a T50 as low as 325 °C, whilst exhibiting excellent stability. After continuous treatment in 10% H2O at 750 °C for 10 h, T50 remains at below 396 °C. The characterization of the catalyst before, after and in situ methane combustion confirms that the high oxygen vacancy concentration and stable PdO nanoparticles both contribute to its excellent activity and stability. The present study introduces a new paradigm for preparing cost-effective and scalable redox catalysts supported on NiAl2O4 spinel with rich and tunable oxygen vacancies.

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
富氧空位 NiAl2O4 支持的钯催化甲烷燃烧性能优越
甲烷催化燃烧是减少天然气燃料发动机温室气体排放的有效解决方案。然而,现有的甲烷燃烧催化剂存在低温活性不足、水热稳定性差等问题。在本研究中,我们证明了在富含氧空位的 NiAl2O4 尖晶石上支撑的 PdO 纳米粒子,通过简单而经济的方法制备,可显著提高 400 °C 以下甲烷燃烧的催化活性。煅烧温度是调节 NiAl2O4 尖晶石中氧空位浓度的有力手段。通过调整钯负载尖晶石催化剂的后续煅烧温度,可有效控制钯氧化物的粒径。优化后的催化剂 Pd/NiAl2O4-900-550(即在 900 °C 下煅烧 NiAl2O4,浸渍 Pd,然后在 550 °C 下煅烧)的 T50 低至 325 °C,同时表现出极佳的稳定性。在 750 °C、10% H2O 条件下连续处理 10 小时后,T50 仍低于 396 °C。催化剂在甲烷燃烧前后和原位燃烧时的表征证实,高氧空位浓度和稳定的氧化钯纳米颗粒都有助于提高催化剂的活性和稳定性。本研究为制备以具有丰富和可调氧空位的 NiAl2O4 尖晶石为支撑的具有成本效益和可扩展的氧化还原催化剂提供了一种新的范例。
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
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
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 Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
期刊最新文献
Hydrolysis of ammonia borane for green hydrogen production over a Pd/C3N4 nanocatalyst synthesized by electron beam irradiation Back cover Single-step in situ synthesis of bimetallic catalysts via a gas-phase route: the case of PdZn–ZnO The effect of polyunsaturation – insights into the hydroformylation of oleochemicals Exploring the impact of abnormal coordination in macrocyclic N-heterocyclic carbene ligands on bio-inspired iron epoxidation catalysis
×
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