检索结果-南通市图书馆

Nickel-based cerium zirconate inorganic complex structures for CO_(2)valorisation via dry reforming of methane

Journal of Environmental Sciences 2024年第6期140卷 12-23页

作者： Juan Luis Martín-Espejo Loukia-Pantzechroula Merkouri Jesús Gándara-Loe José Antonio Odriozola Tomas Ramirez Reina Laura Pastor-Pérez Department of Inorganic Chemistry and Material Sciences Institute of Seville University of Seville-CSICSeville 41092Spain Department of Chemical and Process Engineering University of SurreyGuildford GU27XHUnited Kingdom

The increasing anthropogenic emissions of greenhouse gases(GHG)is encouraging extensive research in CO_(2)utilisation.dry reforming of methane(DRM)depicts a viable strategy to convert both CO_(2)and CH4into syngas,a worthwhile chemical intermediate.Among the different active phases for DRM,the use of nickel as catalyst is economically favourable,but typically deactivates due to sintering and carbon deposition.The stabilisation of Ni at different loadings in cerium zirconate inorganic complex structures is investigated in this work as strategy to develop robust Ni-based DRM catalysts.XRD and TPR-H2analyses confirmed the existence of different phases according to the Ni loading in these materials.Besides,superficial Ni is observed as well as the existence of a CeNiO_(3)perovskite structure.The catalytic activity was tested,proving that 10 wt.%Ni loading is the optimum which maximises conversion.This catalyst was also tested in long-term stability experiments at 600and 800℃in order to study the potential deactivation issues at two different temperatures.At 600℃,carbon formation is the main cause of catalytic deactivation,whereas a robust stability is shown at 800℃,observing no sintering of the active phase evidencing the success of this strategy rendering a new family of economically appealing CO_(2)and biogas mixtures upgrading catalysts.

关键词： CO_(2)conversion dry reforming of methane Nickel catalysts Pyrochlore Cerium zirconate

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

dry reforming of methane on doped Ni nanoparticles:Featureassisted optimizations and ranking of doping metals for direct activations of CH_(4) and CO_(2)

引用

Nano Research 2022年第10期15卷 9670-9682页

作者： Shiru Lin Jean-Baptiste Tristan Yang Wang Junwei Lucas Bao Department of Chemistry Boston CollegeChestnut HillMassachusetts 02467USA Department of Computer Science Boston CollegeChestnut HillMassachusetts 02467USA

As a vital energy resource and raw material for many industrial products,syngas(CO and H_(2))is of great significance.dry reforming of methane(DRM)is an important approach to producing syngas(with a hydrogen-to-carbon-monoxide ratio of 1:1 in principle)from methane and carbon dioxide,with a lower operational cost as compared to other reforming techniques.However,many pure metallic catalysts used in DRM face deactivation issues due to coke formation or sintering of the metal particles.A systematic search for highly efficient metallic catalysts,which reduce the reaction barriers for the rate-determining steps and resist carbon deposition,is urgently needed.Nickel is a typical low-cost transition metal for activating the C–H bond in methane.In this work,we applied a two-step workflow to search for nickel-based bimetallic catalysts with doping metals M(M-Ni)by combining density functional theory(DFT)calculations and machine learning(ML).We focus on the two critical steps in DRM—CH_(4) and CO_(2) direct activations.We used DFT and slab models for the Ni(111)facet to explore the relevant reaction pathways and constructed a data set containing structural and energetic information for representative M-Ni systems.We used this dataset to train ML models with chemical-knowledge-based features and predicted CH_(4) and CO_(2) dissociation energies and barriers,which revealed the composition–activity relationships of the bimetallic catalysts.We also used these models to rank the predicted catalytic performance of candidate systems to demonstrate the applicability of ML for catalyst screening.We emphasized that ML ranking models would be more valuable than regression models in high-throughput screenings.Finally,we used our trained model to screen 12 unexplored M-Ni systems and showed that the DFT-computed energies and barriers are very close to the ML-predicted values for top candidates,validating the robustness of the trained model.

关键词： Ni-based bimetallic catalysts dry reforming of methane syngas production CH_(4)and CO_(2)direct activations ranking model

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

The Nature of Active Sites for Plasmon-Mediated Photothermal Catalysis and Heat-Coupled Photocatalysis in dry reforming of methane

引用

Energy & Environmental Materials 2023年第5期6卷 381-388页

作者： Jinqiang Zhang Liang Wang Xiaoli Zhao Lei Shi Haijun Chen Shu Zhang Peng Zhang Shuaijun Wang Laichang Zhang Yinfeng Wang Xiaoyuan Wang Yuezhao Zhu Huayang Zhang Xiaoguang Duan Mingbo Wu Guosheng Shao Shaobin Wang Hongqi Sun School of Engineering Edith Cowan University 270 Joondalup DriveJoondalup WA 6027Australia Jiangsu Key laboratory of Process Enhancement and New Energy Equipment Technology School of Mechanical and Power EngineeringNanjing Tech UniversityNanjing 211816China College of Materials Science and Engineering Nanjing Forestry UniversityNanjing 210037China School of Materials Science and Engineering Zhengzhou University Zhengzhou 450001China School of Chemical Engineering The University of Adelaide Adelaide South Australia 5005Australia State Key Laboratory of Heavy Oil Processing Institute of New EnergyCollege of Chemical EngineeringChina University of Petroleum(East China)Qingdao 266580China

Solar energy-induced catalysis has been attracting intensive interests and its quantum efficiencies in plasmon-mediated photothermal catalysis(P-photothermal catalysis)and external heat-coupled photocatalysis(E-photothermal catalysis)are ultimately determined by the catalyst structure for photo-induced energetic hot carriers.Herein,different catalysts of supported(TiO_(2)-P25 and Al_(2)O_(3))platinum quantum dots are employed in photo,thermal,and photothermal catalytic dry reforming of methane.Integrated experimental and computational results unveil different active sites(hot zones)on the two catalysts for photo,thermal,and photothermal catalysis.The hot zones of P-photothermal catalysis are identified to be the metal-support interface on Pt/P25 and the Pt surface on Pt/Al_(2)O_(3),respectively.However,a change of the active site to the Pt surface on Pt/P25 is for the first time observed in E-photothermal catalysis(external heating temperature of 700℃).The hot zones contribute to the significant enhancements in photothermal catalytic reactivity against thermocatalysis.This study helps to understand the reaction mechanism of photothermal catalysis to exploit efficient catalysts for solar energy utilization and fossil fuels upgrading.

关键词： dry reforming of methane hot zones photothermal catalysis platinum-based catalysts

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Development and Regeneration Performance of LaNiO_(3)Perovskite Oxides for dry reforming of methane

引用

热科学学报:英文版 2023年第5期32卷 1935-1944页

作者： CAO Dingshan LUO Cong CAI Guoqiu LUO Tong WU Fan LI Xiaoshan ZHENG Ying ZHANG Liqi State Key Laboratory of Coal Combustion School of Energy and Power EngineeringHuazhong University of Science and TechnologyWuhan 430074China

dry reforming of methane(DRM)process has attracted much attention in recent years for the direct conversion of CH_4 and CO_(2)into high-value-added syngas.The key for DRM was to develop catalysts with high activity and stability.In this study,LaNiO_(3)was prepared by the sol-gel,co-precipitation,and hydro-thermal methods to explore the influence of preparation methods on the catalyst structure and DRM reaction performance.The regeneration properties of the used LaNiO_(3)catalysts were also investigated under steam,CO_(2),and air atmospheres,respectively.The results showed that LaNiO_(3)prepared by sol-gel method showed the best DRM performance at 750℃.The DRM performance of the samples prepared by hydro-thermal method was inhibited at 750℃due to the residual of Na^(+)ions during the preparation process.The regeneration tests showed that none of the three atmospheres could restore LaNiO_(3)perovskite phase in the samples,but they could eliminate the carbon deposits in the samples during the DRM reaction,so the samples could maintain stable DRM performance at different cycling stages.

关键词： dry reforming of methane perovskite LaNiO_(3) CO_(2)utilization thermal conversion

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

Utilizing bimetallic catalysts to mitigate coke formation in dry reforming of methane

引用

Journal of Energy Chemistry 2022年第5期31卷 124-142页

作者： Jaylin Sasson Bitters Tina He Elizabeth Nestler Sanjaya D.Senanayake Jingguang G.Chen Cheng Zhang College of Liberal Arts and Sciences Long Island University(Post)BrookvilleNY 11548United States Department of Molecular Biosciences University of Texas at AustinAustinTX 78712United States Chemistry Division Brookhaven National LaboratoryUptonNY 11973United States Department of Chemical Engineering Columbia UniversityNew YorkNY 10027United States

dry reforming of methane(DRM) involves the conversion of carbon dioxide(CO_(2)) and methane(CH_(4)) into syngas(a mixture of hydrogen, H_(2), and carbon monoxide, CO), which can then be used to produce a wide range of products by means of Fischer–Tropsch synthesis. DRM has gained much attention as a means of mitigating damage from anthropogenic greenhouse gas(GHGs) emissions to the environment and instead utilizing these gases as precursors for value-added chemicals or to synthesize sustainable fuels and chemicals. Carbon deposition or coke formation, a primary cause of catalyst deactivation, has proven to be a major challenge in the development of DRM catalysts. The use of nickel-and cobalt-based catalysts has been extensively explored for DRM for their high activity and low cost but suffer from poor stability due to coke formation that has hindered their commercialization. Numerous articles have reviewed the various aspects of catalyst deactivation and strategies for mitigation, but few has focused on the benefit of bimetallic catalysts for mitigating coke formation. Bimetallic catalysts, often improve the catalytic stability over their monometallic counterparts due to synergistic effects resulting from two metal-tometal interactions. This review will cover DRM literature for various bimetallic catalyst systems, including the effect of supports and promoters, on the mitigation of carbonaceous deactivation.

关键词： dry reforming of methane Carbon dioxide Bimetallic catalysts Coke formation Catalyst stability

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

Probing deactivation by coking in catalyst pellets for dry reforming of methane using a pore network model

引用

Chinese Journal of Chemical Engineering 2023年第3期55卷 293-303页

作者： Yu Wang Qunfeng Zhang Xinlei Liu Junqi Weng Guanghua Ye Xinggui Zhou State Key Laboratory of Chemical Engineering School of Chemical EngineeringEast China University of Science and TechnologyShanghai 200237China

dry reforming of methane(DRM) is an attractive technology for utilizing the greenhouse gases(CO_(2) and CH_(4)) to produce syngas. However, the catalyst pellets for DRM are heavily plagued by deactivation by coking, which prevents this technology from commercialization. In this work, a pore network model is developed to probe the catalyst deactivation by coking in a Ni/Al_(2)O_(3) catalyst pellet for DRM. The reaction conditions can significantly change the coking rate and then affect the catalyst deactivation. The catalyst lifetime is higher under lower temperature, pressure, and CH_(4)/CO_(2) molar ratio, but the maximum coke content in a catalyst pellet is independent of these reaction conditions. The catalyst pellet with larger pore diameter, narrower pore size distribution and higher pore connectivity is more robust against catalyst deactivation by coking, as the pores in this pellet are more difficult to be plugged or inaccessible.The maximum coke content is also higher for narrower pore size distribution and higher pore connectivity, as the number of inaccessible pores is lower. Besides, the catalyst pellet radius only slightly affects the coke content, although the diffusion limitation increases with the pellet radius. These results should serve to guide the rational design of robust DRM catalyst pellets against deactivation by coking.

关键词： Deactivation by coking dry reforming of methane Pore network model Diffusion limitation Catalyst pellet

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

Highly dispersed Ni/MgO-mSiO_(2)catalysts with excellent activity and stability for dry reforming of methane

引用

Nano Research 2022年第6期15卷 5004-5013页

作者： Fang Zeng Juan Zhang Run Xu Rongjun Zhang Jianping Ge Shanghai Key Laboratory of Green Chemistry and Chemical Processes School of Chemistry and Molecular EngineeringEast China Normal UniversityShanghai 200062China Department of Coal and Syngas Conversion Research Institute of Petroleum ProcessingSINOPECBeijing 100083China

Highly dispersed Ni catalyst and alkaline promoters supported by mesoporous SiO_(2)nanospheres were synthesized and applied as an active and stable catalyst for dry reforming of methane(DRM).The as-prepared Ni/MgO-mSiO_(2)catalyst showed stable conversions of CH4 and CO_(2)around 82%and 85%in 120 h of DRM reaction,which was superior in performance compared to similar catalysts in literatures.Based on the transmission electron microscope(TEM)images,energy-dispersive spectroscopy(EDS),CO-pulse adsorption,temperature programmed reduction of the oxidized catalysts by hydrogen(H_(2)-TPR),X-ray photoelectron spectroscopy(XPS),temperature-programmed desorption of CO_(2)(CO_(2)-TPD),and thermal gravitational analysis(TGA),the promotion effect of MgO on the Ni catalyst was systematically studied.The introduction of Mg^(2+)in synthesis enhanced the interaction between Ni^(2+)and mSiO_(2),which led to a high dispersion of active centers and a strong“metal–support”interactions to inhibit the sintering and deactivation of Ni at reaction temperatures.On the other hand,Ni and MgO nanoparticles formed adjacently on mSiO_(2),where the“Ni-MgO”interface not only improved the Ni0 distribution and promoted the cracking of CH_(4)but also promoted the activation of CO_(2)and the elimination of carbon deposits.A high and stable conversion of CH4 and CO_(2)were then achieved through the synergistic effect of Ni catalyst,MgO promoter,and mSiO_(2)support.

关键词： Ni-based catalyst dry reforming of methane mesoporous SiO_(2) MgO alkaline

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Photocatalytic dry reforming of methane by rhodium supported monoclinic TiO_(2)-B nanobelts

引用

Journal of Energy Chemistry 2022年第8期31卷 562-571,I0015页

作者： Masaru Kushida Akira Yamaguchi Masahiro Miyauchi School of Materials and Chemical Technology Tokyo Institute of Technology2-12-1 OokayamaMeguro-kuTokyo 152-8552Japan

The conversion of methane and carbon dioxide into syngas(dry reforming of methane;DRM)has attracted attention owing to the potential to reuse greenhouse gases.Titanium dioxide(TiO_(2))-based photocatalysts,which have been widely commercialized owing to their high efficiency,non-toxicity,and low cost,are strongly desired in DRM.Here,we report a monoclinic-phase TiO_(2)-B nanobelts-supported rhodium(Rh/TiO_(2)-B nanobelts)catalyst that efficiently promotes DRM under ultraviolet light irradiation at low temperatures.Photogenerated holes in the TiO_(2)-B nanobelts were used to oxidize methane,while the electrons were trapped in rhodium to reduce carbon dioxide.Rh/TiO_(2)-B nanobelts exhibited considerably higher durability and activity than Rh-loaded conventional TiO_(2)(anatase and rutile),owing to the lattice and/or surface oxygen reactivity in TiO_(2)-B nanobelts,which was suggested by X-ray photoelectron spectroscopy measurements and photocatalytic performance tests under an atmosphere of methane alone.This study paves the path for the effective utilization of methane by constructing active TiO_(2)-based nanometal photocatalysts.

关键词： Photocatalysis dry reforming of methane Greenhouse gas conversion Gas-phase reaction Titanium dioxide TiO_(2)-B

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

Engineering the Interface and Interaction Structure on Highly Coke-Resistant Ni/CeO_(2)-Al_(2)O_(3) Catalyst for dry reforming of methane

引用

Chinese Journal of Structural Chemistry 2022年第12期41卷 7-14页

作者： Sha Li Xin Wang Min Cao Jingjun Lu Li Qiu Xiaoliang Yan College of Chemical Engineering and Technology Taiyuan University of TechnologyTaiyuanShanxi 030024China State Key Laboratory of Clean and Efficient Coal Utilization Taiyuan University of TechnologyTaiyuanShanxi 030024China

Designing and tailoring metal-support interaction in Ni-based catalysts with plentiful interfacial sites is of significant interest for achieving a targeted catalytic performance in dry reforming of methane (DRM),but remains as a challenging task.In this work,Ni/Al_(2)O_(3)and Ni/CeO_(2)-Al_(2)O_(3)catalysts with the same strong metal-support interaction(SMSI) but distinct interface structure are developed by an improved evaporation-induced self-assembly method using pseudobohemite gel as aluminum source.Ni/CeO_(2)-Al_(2)O_(3)exhibits superior catalytic activity and stability in DRM in comparison with Ni/Al_(2)O_(3).The highest CH4and CO_(2)conversion reaches at 71.4%and 82.1%for Ni/CeO_(2)-Al_(2)O_(3),which are higher than that of 64.3% and 75.6% for Ni/Al_(2)O_(3)at 700℃.The SMSI effect in Ni/CeO_(2)-Al_(2)O_(3)provides more active interfacial sites with less coke deposition,and promotes the generation of active formate species which are the key intermediates for DRM.The findings of the present work could possibly pave the way for fabricating catalysts with SMSI strategy for efficient heterogeneous catalysis.

关键词： metal-support interaction interface Ni catalysts CeO_(2) dry reforming of methane

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

Unravelling the Anomalous Coking Resistance over Boron Nitride-Supported Ni Catalysts for dry reforming of methane

引用

CCS Chemistry 2023年第9期5卷 2111-2124页

作者： Jiang Deng Min Gao Jun-ya Hasegawa Xiaoyu Zhang Aiyong Wang Aling Chen Dengsong Zhang International Joint Laboratory of Catalytic Chemistry College of SciencesShanghai UniversityShanghai 200444 Institute for Chemical Reaction Design and Discovery(WPI-ICReDD) Hokkaido UniversitySapporo 001-0021 Institute for Catalysis Hokkaido UniversitySapporo 001-0021

Metal oxides have been used as the supports for heterogeneous catalysis formany years,but they still suffer from coking in some high-temperature applications.The main reasons for coking are the uncontrollable dissociation of C-H and the overbalance between carbon deposition and removal.Herein,we find a boron nitride(BN)-immobilized Ni catalyst shows unprecedented coking resistance in dry reforming of methane via the incomplete decomposition of methane.Unlike the Ni-based catalysts supported by traditional metal oxides,BN-supported Ni accelerates the first C-H dissociation while inhibiting the breaking of the final C-H bond;hence,the suppression of the complete decomposition of methane thoroughly addresses the coking issue.This work reveals the fundamental reason for the coking resistance over BN-supported Ni catalysts is selective activation of the C-H bond,which can provide an inspiring idea for other applications.

关键词： heterogenous catalysis boron nitrides dry reforming of methane coking resistance methane conversion

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

欢迎您,

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

请选择保存的检索档案：

请选择收藏分类：

通借通还

欢迎您,

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：