InfluenceofZr,Ce,andLaonCo3O4catalystforCO2methanationatlowtemperature

被引:3
作者
Yuwen Zhou [1 ]
Yuexiu Jiang [1 ]
Zuzeng Qin [1 ,2 ]
Qinruo Xie [3 ]
Hongbing Ji [1 ,2 ]
机构
[1] School of Chemistry and Chemical Engineering, Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, Guangxi University
[2] School of Chemistry, Sun Yat-sen University
[3] School of Biology and Chemical Engineering, Guangxi University of Science and Technology
关键词
CO2; hydrogenation; Methanation; Co3O4; catalyst; Cobalt-zirconium interaction; Basic sites;
D O I
暂无
中图分类号
TQ426 [催化剂(触媒)];
学科分类号
080502 ; 081705 ;
摘要
The Co3O4 and Zr-,Ce-,and La-Co3O4 catalysts were prepared,characterized,and applied to produce CH4 from CO2 catalytic hydrogenation in low temperature as 140–220°C.The results indicated that the addition of Zr,Ce,or La to the Co3O4 decreased the crystallite sizes of Co and the outer-shell electron density of Co3+,and increased the specific surface area,which would provide more active sites for the CO2 methanation.Especially,the addition of Zr also changed the reducing state of Co3O4 via an obvious change in the interaction between Co3O4 and ZrO2.Furthermore,Zr doped into the Co3O4 increased the basic intensity of the weak and medium basic sites,as well as the amount of Lewis acid sites,and Br?nsted acid sites were also found on the Zr-Co3O4 surface.The introduction of Zr,Ce,or La favored the production of CH4,and the Zr-Co3O4catalyst exhibited the highest CO2 conversion(58.2%)and CH4 selectivity(100%)at 200°C,and 0.5 MPa with a gaseous hourly space velocity of 18,000 ml·g-1cat·h-1,and the catalytic activity of CO2methanation for the Zr-,Ce-,and La-Co3O4 exhibited more stable than Co3O4 in a 20-h reaction.
引用
收藏
页码:768 / 774
页数:7
相关论文
共 27 条
[1]   CO2methanationoverTiO2–Al2O3binaryoxidessupportedRucatalysts [J].
Jinghua Xu ;
Qingquan Lin ;
Xiong Su ;
Hongmin Duan ;
Haoran Geng ;
Yanqiang Huang .
Chinese Journal of Chemical Engineering, 2016, 24 (01) :140-145
[2]  
Catalytic performance of cement clinker supported nickel catalyst in glycerol dry reforming[J]. Hua Chyn Lee,Kah Weng Siew,Maksudur R.Khan,Sim Yee Chin,Jolius Gimbun,Chin Kui Cheng.Journal of Energy Chemistry. 2014(05)
[3]   CO2在高分散Ni/La2O3催化剂上的甲烷化 [J].
宋焕玲 ;
杨建 ;
赵军 ;
丑凌军 .
催化学报, 2010, 31 (01) :21-23
[4]  
Synthesis of lanthanide series (La, Ce, Pr, Eu & Gd) promoted Ni/γ-Al2O3 catalysts for methanation of CO2 at low temperature under atmospheric pressure[J] . Waqar Ahmad,Muhammad Naeem Younis,Reyad Shawabkeh,Shakeel Ahmed.Catalysis Communications . 2017
[5]  
Hydrogenation of CO 2 to dimethyl ether on La-, Ce-modified Cu-Fe/HZSM-5 catalysts[J] . Zu-zeng Qin,Xin-hui Zhou,Tong-ming Su,Yue-xiu Jiang,Hong-bing Ji.Catalysis Communications . 2016
[6]  
Effects of Lewis acidity of metal oxide promoters on the activity and selectivity of Co-based Fischer–Tropsch synthesis catalysts[J] . Gregory R. Johnson,Alexis T. Bell.Journal of Catalysis . 2016
[7]  
A highly active and stable Co 4 N/γ-Al 2 O 3 catalyst for CO and CO 2 methanation to produce synthetic natural gas (SNG)[J] . Rauf Razzaq,Chunshan Li,Muhammad Usman,Kenzi Suzuki,Suojiang Zhang.Chemical Engineering Journal . 2015
[8]  
CO 2 hydrogenation into CH 4 on NiHNaUSY zeolites[J] . I. Gra?a,L.V. González,M.C. Bacariza,A. Fernandes,C. Henriques,J.M. Lopes,M.F. Ribeiro.Applied Catalysis B: Environmental . 2014
[9]   Carbon Dioxide Methanation on Ordered Mesoporous Co/KIT-6 Catalyst [J].
Zhou, Guilin ;
Wu, Tian ;
Zhang, Haibing ;
Xie, Hongmei ;
Feng, Yongcheng .
CHEMICAL ENGINEERING COMMUNICATIONS, 2014, 201 (02) :233-240
[10]   Effects of structure on the carbon dioxide methanation performance of Co-based catalysts [J].
Zhou, Guilin ;
Wu, Tian ;
Xie, Hongmei ;
Zheng, Xuxu .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2013, 38 (24) :10012-10018