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反应气中活化后的镍酸镧用于二氧化碳加氢生成甲烷
引用本文:高敬,贾立山,方维平,李清彪,宋浩.反应气中活化后的镍酸镧用于二氧化碳加氢生成甲烷[J].燃料化学学报,2009,37(5):573-577.
作者姓名:高敬  贾立山  方维平  李清彪  宋浩
作者单位:1.Department of Chemical Engineering and Biochemical Engineering, College of Chemistry and Chemical Engineering, ; Xiamen University, Xiamen 361005, China; 2.Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China; 3.National Engineering Laboratory for Green Chemical Productions of Alcohols, Ethers and Esters, Xiamen 361005, China
基金项目:National Engineering Laboratory for Green Chemical Productions of Alcohols,Ethers and Esters and State Key Laboratory for Physical Chemistry of Solid Surface of Xiamen University
摘    要:采用柠檬酸法制备了钙钛矿镍酸镧,并将其作为催化剂的前躯体用于二氧化碳甲烷化反应中。催化剂在400℃~700℃温度下反应气中进行活化处理。活化过程中生成了金属镍颗粒和碳酸氧化镧。金属镍呈高度分散状并被碳酸氧化镧包裹,这种现象有助于反应在400℃和500℃的高温下仍保持高活性和稳定性。XRD、XPS、TEM和H2-TPD等表征测试表明,在活化过程中生成的碳酸氧化镧对反应起到了至关重要的作用。

关 键 词:镍酸镧  钙钛矿  二氧化碳甲烷化  活化  碳酸氧化镧  
收稿时间:2009-03-04
修稿时间:2009-06-08

Methanation of carbon dioxide over the LaNiO3 perovskite catalysts activated under the reactant stream
GAO Jing,JIA Li-shan,FANG Wei-ping,LI Qing-biao,SONG Hao.Methanation of carbon dioxide over the LaNiO3 perovskite catalysts activated under the reactant stream[J].Journal of Fuel Chemistry and Technology,2009,37(5):573-577.
Authors:GAO Jing    JIA Li-shan  FANG Wei-ping  LI Qing-biao  SONG Hao
Institution:1.Department of Chemical Engineering and Biochemical Engineering;College of Chemistry and Chemical Engineering;Xiamen University;Xiamen 361005;China;2.Department of Chemistry;3.National Engineering Laboratory for Green Chemical Productions of Alcohols;Ethers and Esters;China
Abstract:In this study, LaNiO3 perovskite catalysts were prepared by citrate method and used for carbon dioxide (CO2) methanation. The catalysts were activated at different temperatures (400℃~700℃) under the reactant stream. The activation led to the formation of small metallic nickel particles and hexagonal lanthanum oxocarbonate (La2O2CO3). Ni0 was highly dispersed and enveloped by La2O2CO3, which was responsible for the high catalytic activity and stability of the LaNiO3 perovskite catalysts even at high temperature (400℃~500℃). The X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, and H2-temperature-programmed desorption measurements illustrated that La2O2CO3 generated from the activation might play an important role in the methanation of CO2.
Keywords:LaNiO3  perovskite  CO2 methanation  activation  La2O2CO3  
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