Ni Particle Morphology and Support Effect in the Catalytic Decomposition of Methane: Into the Design of Novel, High Yield Catalyst for Catalytic Decomposition of Methane

IF 6.2 Q2 ENERGY & FUELS
Jose A. Hernandez Gaitan, Xinyu Li, Kazuya Tamura, Koji Miyake, Yoshiaki Uchida, Norikazu Nishiyama
{"title":"Ni Particle Morphology and Support Effect in the Catalytic Decomposition of Methane: Into the Design of Novel, High Yield Catalyst for Catalytic Decomposition of Methane","authors":"Jose A. Hernandez Gaitan,&nbsp;Xinyu Li,&nbsp;Kazuya Tamura,&nbsp;Koji Miyake,&nbsp;Yoshiaki Uchida,&nbsp;Norikazu Nishiyama","doi":"10.1002/aesr.202400096","DOIUrl":null,"url":null,"abstract":"<p>Research on high-surface-area supports and synergic promoters has been made, however, there is still much room for improvement on the catalytic-particles morphology and interaction with the support. A first approach for designing nanoplate supports to improve CDM catalysts was made. Amorphous aluminosilicates nanoplates (a-AS.np) with an average particle size of 23.4 nm and an average height of 2.8 nm, and α-Ni(OH)<sub>2</sub> nanoplates (Ni.np) with an average particle size of 23.2 nm and an average thickness of 8.4 nm, were successfully synthesized, using a two-dimensional reactor in amphiphilic phases (TRAP). Nickel loaded in a-AS materials with different morphologies and promotion effects of lantana (La<sup>3+</sup>) &amp; chromium (Cr<sup>3+</sup>) species were studied. La-Cr promoted a-AS support showed an average increase of 13% on H<sub>2</sub> yield in severe conditions due to improved crystallization of Ni particles on mesoporous support and the electron promotion of La to Ni species. Furthermore, we evaluate the Ni.np as novel morphology support for La<sup>3+</sup> &amp; copper (Cu<sup>2+</sup>) species in the methane decomposition reaction. La-Cu Ni.np showed outstanding performance and stability, a max H<sub>2</sub> yield of 15.9% (at 700 °C), and more than 400 min of H<sub>2</sub> generation (at 550 °C) compared to its a-AS support counterparts.</p>","PeriodicalId":29794,"journal":{"name":"Advanced Energy and Sustainability Research","volume":"5 9","pages":""},"PeriodicalIF":6.2000,"publicationDate":"2024-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aesr.202400096","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Energy and Sustainability Research","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/aesr.202400096","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0

Abstract

Research on high-surface-area supports and synergic promoters has been made, however, there is still much room for improvement on the catalytic-particles morphology and interaction with the support. A first approach for designing nanoplate supports to improve CDM catalysts was made. Amorphous aluminosilicates nanoplates (a-AS.np) with an average particle size of 23.4 nm and an average height of 2.8 nm, and α-Ni(OH)2 nanoplates (Ni.np) with an average particle size of 23.2 nm and an average thickness of 8.4 nm, were successfully synthesized, using a two-dimensional reactor in amphiphilic phases (TRAP). Nickel loaded in a-AS materials with different morphologies and promotion effects of lantana (La3+) & chromium (Cr3+) species were studied. La-Cr promoted a-AS support showed an average increase of 13% on H2 yield in severe conditions due to improved crystallization of Ni particles on mesoporous support and the electron promotion of La to Ni species. Furthermore, we evaluate the Ni.np as novel morphology support for La3+ & copper (Cu2+) species in the methane decomposition reaction. La-Cu Ni.np showed outstanding performance and stability, a max H2 yield of 15.9% (at 700 °C), and more than 400 min of H2 generation (at 550 °C) compared to its a-AS support counterparts.

Abstract Image

甲烷催化分解过程中的镍颗粒形态和支撑效应:新型高产甲烷催化分解催化剂的设计初探
对高表面积载体和协同促进剂的研究已经取得了一些成果,但催化颗粒的形态以及与载体的相互作用仍有很大的改进空间。为改进清洁发展机制催化剂而设计纳米平板支撑物的方法初见端倪。利用两亲相二维反应器(TRAP)成功合成了平均粒径为 23.4 纳米、平均高度为 2.8 纳米的无定形铝硅酸盐纳米板(a-AS.np)和平均粒径为 23.2 纳米、平均厚度为 8.4 纳米的α-Ni(OH)2 纳米板(Ni.np)。研究了具有不同形态的 a-AS 材料中的镍负载以及镧(La3+)和amp;铬(Cr3+)物种的促进作用。La-Cr 促进的 a-AS 支持物在苛刻条件下的 H2 产率平均提高了 13%,这是由于镍颗粒在介孔支持物上的结晶得到了改善,以及 La 对镍物种的电子促进作用。此外,我们还评估了 Ni.np 在甲烷分解反应中作为 La3+ & 铜 (Cu2+) 物种的新型形态支撑的效果。与 a-AS 支持物相比,La-Cu Ni.np 表现出卓越的性能和稳定性,最大 H2 产率为 15.9%(700 °C),H2 生成时间超过 400 分钟(550 °C)。
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
CiteScore
8.20
自引率
3.40%
发文量
0
期刊介绍: Advanced Energy and Sustainability Research is an open access academic journal that focuses on publishing high-quality peer-reviewed research articles in the areas of energy harvesting, conversion, storage, distribution, applications, ecology, climate change, water and environmental sciences, and related societal impacts. The journal provides readers with free access to influential scientific research that has undergone rigorous peer review, a common feature of all journals in the Advanced series. In addition to original research articles, the journal publishes opinion, editorial and review articles designed to meet the needs of a broad readership interested in energy and sustainability science and related fields. In addition, Advanced Energy and Sustainability Research is indexed in several abstracting and indexing services, including: CAS: Chemical Abstracts Service (ACS) Directory of Open Access Journals (DOAJ) Emerging Sources Citation Index (Clarivate Analytics) INSPEC (IET) Web of Science (Clarivate Analytics).
×
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:481959085
Book学术官方微信