Transactions of Nonferrous Metals Society of China The Chinese Journal of Nonferrous Metals

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中国有色金属学报

ZHONGGUO YOUSEJINSHU XUEBAO

第14卷    第9期    总第66期    2004年9月

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文章编号:1004-0609(2004)09-1580-05
钙钛矿催化材料La1-xCexCoO3+δ的制备、
表征及甲烷燃烧催化性质
 崔梅生, 李明来, 张顺利, 龙志奇, 
崔大立, 黄小卫

( 北京有色金属研究总院 有研稀土新材料股份有限公司,  北京 100088)

摘 要: 采用柠檬酸发泡法制备了钙钛矿LaCoO3催化材料;研究了Ce对La进行掺杂替代对催化材料性能的影响;通过BET、 XRD、 SEM等手段对催化材料进行了物性表征; 以甲烷完全燃烧为目标反应, 研究了钙钛矿La1-xCexCoO3+δ的催化性能。 结果表明: 铈掺杂对材料晶相有较大影响, 当掺杂量x小于0.3时, 粉体晶型基本不变, 而当掺杂量达到0.5时, 有明显CO3O4晶相出现, LaCoO3钙钛矿晶相完整性遭到破坏, 当掺杂量大于0.7时, 钙钛矿晶相大大弱化甚至消失;  LaCoO3是一种性能优良的甲烷燃烧催化材料, Ce的掺杂替代对催化材料活性有明显影响, 并增强了催化材料的高温稳定性能, 铈最佳掺杂量为0.3;  前驱体经700 ℃焙烧形成了较为完整的钙钛矿晶型, 经800 ℃焙烧后, 催化材料最高活性为: t10%=390 ℃, t90%=603 ℃。 

 

关键字: 柠檬酸; 钙钛矿; 甲烷; 催化燃烧; 稀土

Preparation and physico-chemical characterisation of 
La1-xCexCoO3+δ perovskite catalyst and its methane catalytic combustion
CUI Mei-sheng, LI Ming-lai, ZHANG Shun-li, 
LONG Zhi-qi, CUI Da-li, HUANG Xiao-wei

Grirem Advanced Materials Co. Ltd,
General Research Institute for Non-ferrous Metals, Beijing 100088, China

Abstract: Perovskite oxides LaCoO3 methane catalytic materials were prepared with citrate complexation and bubbling method. The cerium doping effect was studied in series La1-xCexCoO3+δ materials by BET, XRD and SEM techniques. And their catalytic behaviours were also studied with methane catalytic complete combustion as probe reaction. The results show that doped cerium has great effects on the crystal phase formed. When doped cerium content x is less than 0.3, the phases of powders are little changed. When doped cerium x is up to 0.5, obvious Co3O4 phase is discovered, and the integrity of LaCoO3 perovskite crystal phase is broken. When x is over 0.7, perovskite crystal phase is greatly weakened or completely disappeared. Considering the crystal phase of powders, the optimum cerium doping content is about 0.3. Perovskite oxides LaCoO3 are good methane catalytic materials. Doping cerium has some positive activity effect and the thermal stability of the material is also enhanced. The perovskite oxide can be formed at lower calcination temperature, about 700 ℃, and when x is 0.3, the best catalytic activity is acquired as t10%=390 ℃ and t90%=603 ℃ in series of La1-xCexCoO3+δ materials calcinated at 800 ℃.

 

Key words: citric acid; perovskite; methane; catalytic combustion; rare earth

ISSN 1004-0609
CN 43-1238/TG
CODEN: ZYJXFK

ISSN 1003-6326
CN 43-1239/TG
CODEN: TNMCEW

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