Kinetic Coupling of Steady-State Dry Reforming of Methane and Self-Oscillating Partial Oxidation of Methane over Nickel

IF 1.3 4区 化学 Q4 CHEMISTRY, PHYSICAL Kinetics and Catalysis Pub Date : 2024-09-04 DOI:10.1134/S002315842460175X
V. Yu. Bychkov, Yu. P. Tulenin, Yu. A. Gordienko, O. N. Sil’chenkova, V. N. Korchak
{"title":"Kinetic Coupling of Steady-State Dry Reforming of Methane and Self-Oscillating Partial Oxidation of Methane over Nickel","authors":"V. Yu. Bychkov,&nbsp;Yu. P. Tulenin,&nbsp;Yu. A. Gordienko,&nbsp;O. N. Sil’chenkova,&nbsp;V. N. Korchak","doi":"10.1134/S002315842460175X","DOIUrl":null,"url":null,"abstract":"<p>The occurrence of dry reforming of methane (DRM) in a steady-state mode and partial oxidation of methane (POM) in a self-oscillating mode over a nickel foil sample and the simultaneous occurrence of these two reactions have been studied. It has been shown that during the cooccurrence of the DRM and POM reactions, a kinetic coupling of these reactions takes place; it is evident as a change in the self-oscillation period and a significant acceleration of the DRM reaction in certain phases of the self-oscillation cycle compared with the DRM rate over this Ni sample in a steady-state mode. The DRM acceleration effect is observed in a temperature range of 600–750°C. The maximum increase in the CO<sub>2</sub> conversion value averaged over the oscillation period is a factor of 2.6 at a temperature of 700°C for a feed gas mixture composition of CH<sub>4</sub> : CO<sub>2</sub> = 1 : 1 + 3.5% O<sub>2</sub>. In addition, the effect of O<sub>2</sub> concentration in a range of 0.5–3.5% on the increase in the DRM rate has been studied. An interpretation of the observed effects has been proposed.</p>","PeriodicalId":682,"journal":{"name":"Kinetics and Catalysis","volume":"65 4","pages":"405 - 412"},"PeriodicalIF":1.3000,"publicationDate":"2024-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kinetics and Catalysis","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S002315842460175X","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

The occurrence of dry reforming of methane (DRM) in a steady-state mode and partial oxidation of methane (POM) in a self-oscillating mode over a nickel foil sample and the simultaneous occurrence of these two reactions have been studied. It has been shown that during the cooccurrence of the DRM and POM reactions, a kinetic coupling of these reactions takes place; it is evident as a change in the self-oscillation period and a significant acceleration of the DRM reaction in certain phases of the self-oscillation cycle compared with the DRM rate over this Ni sample in a steady-state mode. The DRM acceleration effect is observed in a temperature range of 600–750°C. The maximum increase in the CO2 conversion value averaged over the oscillation period is a factor of 2.6 at a temperature of 700°C for a feed gas mixture composition of CH4 : CO2 = 1 : 1 + 3.5% O2. In addition, the effect of O2 concentration in a range of 0.5–3.5% on the increase in the DRM rate has been studied. An interpretation of the observed effects has been proposed.

Abstract Image

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
甲烷在镍上的稳态干法重整与甲烷的自振荡部分氧化的动力学耦合
摘要 研究了在镍箔样品上以稳态模式发生的甲烷干重整(DRM)和以自振模式发生的甲烷部分氧化(POM),以及这两种反应同时发生的情况。研究表明,在 DRM 和 POM 反应同时发生期间,这两种反应发生了动力学耦合;这表现为自振荡周期的变化,以及在自振荡周期的某些阶段,与稳态模式下该镍样品上的 DRM 反应速率相比,DRM 反应明显加速。在 600-750°C 的温度范围内观察到了 DRM 加速效应。在 CH4 : CO2 = 1 : 1 + 3.5% O2 的原料气混合物成分条件下,700°C 的温度下 CO2 转化值的最大增幅为 2.6 倍。此外,还研究了 0.5%-3.5%范围内的氧气浓度对 DRM 增长率的影响。对观察到的影响提出了解释。
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
Kinetics and Catalysis
Kinetics and Catalysis 化学-物理化学
CiteScore
2.10
自引率
27.30%
发文量
64
审稿时长
6-12 weeks
期刊介绍: Kinetics and Catalysis Russian is a periodical that publishes theoretical and experimental works on homogeneous and heterogeneous kinetics and catalysis. Other topics include the mechanism and kinetics of noncatalytic processes in gaseous, liquid, and solid phases, quantum chemical calculations in kinetics and catalysis, methods of studying catalytic processes and catalysts, the chemistry of catalysts and adsorbent surfaces, the structure and physicochemical properties of catalysts, preparation and poisoning of catalysts, macrokinetics, and computer simulations in catalysis. The journal also publishes review articles on contemporary problems in kinetics and catalysis. The journal welcomes manuscripts from all countries in the English or Russian language.
期刊最新文献
Photocatalytic Activity of Heterostructures Based on Graphite-Like Carbon Nitride Modified with Few-Layer Black Phosphorus and Cobalt Phosphide in the Hydrogen Evolution Reaction Reassembled Nanosheets of Layered Perovskite-Like Niobate HCa2Nb3O10 as Photocatalysts for Hydrogen Production from Aqueous Solutions of Plant Biomass Processing Products Oxygen-Free Reforming of Methane into Synthesis Gas in the Presence of H2, H2O, CO, and CO2 Additives Taking into Account the Formation of Soot Particles Aromatic Cross-Conjugated Hydrazones as Inhibitors of the Radical Chain Oxidation of Styrene Photocatalysis for Energy, Environmental Protection, and Sustainable Development
×
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