Recent Advances on Nitrous Oxide (N2O) Decomposition over Non-Noble-Metal Oxide Catalysts: Catalytic Performance, Mechanistic Considerations, and Surface Chemistry Aspects

催化作用 贵金属 氧化物 环境修复 一氧化二氮 化学 分解 纳米技术 材料科学 无机化学 有机化学 生态学 生物 污染
作者
Michalis Konsolakis
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:5 (11): 6397-6421 被引量:437
标识
DOI:10.1021/acscatal.5b01605
摘要

Nitrous oxide (N2O) is the largest stratospheric-ozone-depleting substance, being concomitantly the third most potent greenhouse gas. The direct catalytic decomposition of N2O (deN2O process) is one of the most promising remediation technologies for N2O emissions abatement. Although noble metals (NMs)-based catalysts demonstrate satisfactory deN2O performance, their high cost and sensitivity to various effluent stream components (e.g., water vapor, oxygen) limit their widespread industrial applications. Hence, the development of NMs-free catalysts of low cost and satisfactory deN2O performance is of paramount importance. This survey appraises the recent advances, which have been reported since 2000, on N2O decomposition over non-noble-metal oxidic catalysts. Initially, a brief overview of N2O sources, environmental consequences, and remediation technologies is provided. The literature related to the deN2O process over NMs-free metal oxides (MOs) is categorized and critically discussed, as follows: (i) bare oxides, (ii) hexaaluminates, (iii) hydrotalcites, (iv) spinels, (v) perovskites, and (iv) mixed metal oxides not belonging in the above categories. This review covers several aspects with respect to the reaction mechanisms, the structure–activity correlations, the role of various inhibitors (e.g., O2, NO, H2O) as well as the strategies followed to adjust the local surface structure of MOs. Fundamental insights toward fine-tuning of surface chemistry of MOs by means of advanced preparation routes and/or electronic promotion are also provided, paving the way for real-life energy and environmental applications, beyond the deN2O process.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
JamesPei应助六六采纳,获得30
刚刚
小马甲应助Hey采纳,获得10
1秒前
hkh发布了新的文献求助10
1秒前
可乐不加冰完成签到,获得积分10
1秒前
含蓄含烟完成签到,获得积分10
1秒前
printzhao完成签到,获得积分10
1秒前
MYMELODY完成签到,获得积分10
2秒前
锋回露转123完成签到,获得积分10
2秒前
开心的谷兰完成签到,获得积分10
2秒前
yao发布了新的文献求助10
2秒前
姜jiang完成签到,获得积分10
2秒前
余长青完成签到 ,获得积分10
3秒前
3秒前
Ligin发布了新的文献求助10
3秒前
粗心的妙芹完成签到,获得积分10
3秒前
gggggs完成签到,获得积分10
3秒前
uu应助追寻紫安采纳,获得10
3秒前
leezhen完成签到,获得积分10
4秒前
Dylan完成签到,获得积分10
4秒前
土豆完成签到,获得积分10
4秒前
FFFFFF完成签到 ,获得积分10
4秒前
余任游完成签到,获得积分10
4秒前
live完成签到 ,获得积分10
4秒前
方雪冰发布了新的文献求助10
5秒前
脑洞疼应助科研通管家采纳,获得10
5秒前
老福贵儿应助科研通管家采纳,获得10
5秒前
科目三应助科研通管家采纳,获得10
5秒前
5秒前
团团完成签到,获得积分10
5秒前
项芯涵完成签到,获得积分10
5秒前
CodeCraft应助可爱的妙海采纳,获得10
5秒前
陈砍砍完成签到 ,获得积分10
6秒前
Math4396完成签到 ,获得积分10
6秒前
科研通AI6.1应助yuquan采纳,获得10
6秒前
调皮老头完成签到,获得积分10
7秒前
刘逸飞完成签到,获得积分10
7秒前
务实水池完成签到,获得积分10
7秒前
gege完成签到,获得积分10
8秒前
MQhhh完成签到,获得积分10
8秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
PowerCascade: A Synthetic Dataset for Cascading Failure Analysis in Power Systems 2000
Picture this! Including first nations fiction picture books in school library collections 1500
Signals, Systems, and Signal Processing 610
Unlocking Chemical Thinking: Reimagining Chemistry Teaching and Learning 555
CLSI M100 Performance Standards for Antimicrobial Susceptibility Testing 36th edition 400
Cancer Targets: Novel Therapies and Emerging Research Directions (Part 1) 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6362519
求助须知:如何正确求助?哪些是违规求助? 8176319
关于积分的说明 17226937
捐赠科研通 5417279
什么是DOI,文献DOI怎么找? 2866743
邀请新用户注册赠送积分活动 1843899
关于科研通互助平台的介绍 1691640