Stabilizing Supported Ni Catalysts for Dry Reforming of Methane by Combined La Doping and Al Overcoating Using Atomic Layer Deposition

甲烷 催化作用 图层(电子) 兴奋剂 沉积(地质) 原子层沉积 诱导期 金属 化学工程 铝酸盐 材料科学 二氧化碳重整 相(物质) 化学 无机化学 纳米技术 冶金 合成气 有机化学 工程类 光电子学 古生物学 生物 水泥 沉积物
作者
Sol Ahn,Patrick Littlewood,Yiqi Liu,Tobin J. Marks,Peter C. Stair
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:12 (17): 10522-10530 被引量:32
标识
DOI:10.1021/acscatal.2c02599
摘要

Deposition of La2O3 and Al2O3 on Al2O3-supported Ni catalysts was performed to study their effects on heterogeneous catalysts for the dry reforming of methane (DRM) reaction. An alumina-supported Ni catalyst (Ni/Al2O3, 2 wt % of Ni), synthesized via incipient wetness impregnation, loses ∼87% of its initial activity within 45 h under DRM conditions. While overcoating of Al2O3 on this catalyst via atomic layer deposition (ALD) helps stabilize the catalytic activity in long time-on-stream (TOS) tests, this overcoated catalyst is ca. 40 times less active than the uncoated catalyst at peak activity. This Al2O3-overcoated Ni/Al2O3 catalyst also exhibits a long induction period (∼20 h) due to the slow reduction of Ni2+ within the catalytically inactive nickel aluminate (NiAl2O4) phase, formed by the interaction of metallic Ni with the Al2O3 overcoat during pre-DRM treatment at the 700 °C reaction temperature. Here, we report that, while doping small amounts of La (∼0.03 wt %) into the Ni/Al2O3 catalyst does not significantly affect the catalytic activity or stability by itself, the addition of ALD-Al2O3 on top of the La2O3-promoted Ni catalysts significantly suppresses the long TOS deactivation, helps recover the peak activity of uncoated Ni/Al2O3, and eliminates the DRM induction period. This strategy obtains the stabilization benefits of Al2O3 overcoating on Ni/Al2O3 while, at the same time, avoiding the formation of undesirable NiAl2O4 species.
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
仙贝发布了新的文献求助10
刚刚
panpan发布了新的文献求助10
刚刚
1秒前
1秒前
君无邪发布了新的文献求助10
2秒前
2秒前
领导范儿应助失眠洋葱采纳,获得10
2秒前
星辰于我关注了科研通微信公众号
2秒前
心碎小漏完成签到,获得积分20
2秒前
喜悦灯泡发布了新的文献求助10
2秒前
2秒前
2秒前
开朗天菱发布了新的文献求助10
3秒前
xuxxx完成签到,获得积分10
3秒前
大意的画板完成签到,获得积分10
3秒前
盘菜应助科研通管家采纳,获得10
4秒前
太叔开山发布了新的文献求助10
4秒前
完美世界应助科研通管家采纳,获得10
4秒前
NexusExplorer应助科研通管家采纳,获得10
4秒前
4秒前
无花果应助科研通管家采纳,获得10
4秒前
科研通AI2S应助科研通管家采纳,获得10
4秒前
852应助科研通管家采纳,获得10
4秒前
今后应助科研通管家采纳,获得10
5秒前
Curiosity应助科研通管家采纳,获得10
5秒前
慕青应助科研通管家采纳,获得10
5秒前
慕青应助科研通管家采纳,获得30
5秒前
深情安青应助科研通管家采纳,获得10
5秒前
小梅姐应助科研通管家采纳,获得10
6秒前
摇摆小狗发布了新的文献求助10
6秒前
FashionBoy应助科研通管家采纳,获得10
6秒前
why发布了新的文献求助10
6秒前
Mic应助科研通管家采纳,获得10
6秒前
研友_VZG7GZ应助mengdewen采纳,获得50
6秒前
深情安青应助科研通管家采纳,获得10
6秒前
小梅姐应助科研通管家采纳,获得10
6秒前
追寻微笑应助科研通管家采纳,获得10
6秒前
田様应助科研通管家采纳,获得100
7秒前
7秒前
Hello应助科研通管家采纳,获得10
7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
An Introduction to Foreign Language Learning and Teaching 750
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
What is the Future of Psychotherapy in Digital Age? Technology, AI Bots, and Psychotherapy after Covid 444
Synthesis of P-Chiral Phosphine Ligands and Their Applications in Asymmetric Catalysis 400
Management and the Arts 310
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 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7630098
求助须知:如何正确求助?哪些是违规求助? 9204738
关于积分的说明 19738683
捐赠科研通 7199749
什么是DOI,文献DOI怎么找? 3274425
关于科研通互助平台的介绍 2436516
邀请新用户注册赠送积分活动 2270663