期刊文献+

SO_2对La_(0.8)K_(0.2)Cu_(0.05)Mn_(0.95)O_3钙钛矿催化剂氧化碳烟的影响 被引量:4

Effect of SO_2 on Soot Oxidation over La_(0.8)K_(0.2)Cu_(0.05)Mn_(0.95)O_3 Perovskites-type Catalyst
在线阅读 下载PDF
导出
摘要 采用柠檬酸配位法制备K、Cu掺杂的La0.8K0.2Cu0.05Mn0.95O3钙钛矿催化剂,运用程序升温氧化(TPO)考察在不同浓度SO2气氛下La0.8K0.2Cu0.05Mn0.95O3催化剂催化氧化模拟碳黑的性能,并用XRD、FTIR和XPS等进行表征。结果表明,催化剂在0~0.1%的SO2气氛中呈现出不同活性,φSO2≤0.05%的气氛可促进催化剂催化氧化碳黑的活性,当φSO2=0.03%时,催化剂活性最高;引入φSO2≥0.06%时催化剂活性明显下降。XPS说明表面活性氧的增加是低浓度的SO2促进催化活性的原因,同时XRD、FTIR结果表明高浓度的SO2所产生的大量SO42-是抑制催化剂活性的原因。 La0.8K0.2Cu0.05Mn0.95O3 catalysts were prepared using the citrate acid-complex combustion method. Catalysts were characterized with XRD, FTIR, XPS. Temperature programmed oxidation(TPO) tests were performed to evaluate the catalytic activity for soot oxidation in a feed gas containing various concentrations of SO2. The TPO results revealed that the catalysts exhibited different activities with 0-0.1% SO2 in feed gas. The performance of the catalyst was enhanced with SO2 concentration below 0.05%, and 0.03% SO2 resulted in the highest activity. However, the soot oxidation rate decreased when the SO2 feed concentration was above 0.06%. The results of XPS indicated that the increase of weakly chemisorbed O^- surface species was responsible for the excellent performance of La0.8K0.2Cu0.05Mn0.95O3 with lower concentration of SO2. The XRD and FTIR results revealed that plentiful SO4^2- was produced on the catalyst surface when SO2 coneentration was high, which could account for the loss of activity of the La0.8K0.2Cu0.05Mn0.95O3 catalyst.
出处 《无机化学学报》 SCIE CAS CSCD 北大核心 2009年第7期1170-1176,共7页 Chinese Journal of Inorganic Chemistry
基金 广东高校科技成果转化项目[No.粤教科(2009)13号(cgzhzd0803)] 广东省自然科学基金(No.8151009101000025) 广东省社会发展科技(No.2007B030102006) 广州市属高校科技项目(No.62008)资助
关键词 二氧化硫 钙钛矿催化剂 碳烟氧化 表面活性氧 sulfur dioxide perovskites-type catalyst soot oxidation superficial oxygen
  • 相关文献

参考文献27

  • 1Peralta M A,Milt V G,Cornaglia L M,et al.J.Coral,2006,242:118~130
  • 2CHEN Yu(陈瑜),YE Dai-Qi(叶代启),FU Ming-Li(付名利),et al.Acta Scientiate Circumstantiate (Huanjing Kexue Xuebao),2008,28(11):2167~2174
  • 3LIANG Hong(梁红),LI Shu-Hua(李树华),ZHONG Zhi-Jian(钟志剑),et al.J.Guangzhou Univ.(Guangzhou Daxue Xuebao),2006,5(5):30~32[41 Teraoka Y,Hanada H,Hagawa S.Appl.Catal.B:Environ.,2001,34:73~78
  • 4WANG Hong(王虹),ZHAO Zheng(赵霞),LIU Jian (刘坚),et al.Chin.Sci,Bull.(Kexue Tongbao),2005,50 (4):336~339
  • 5PENG Xiao-Sheng(彭小对),LIN He(林赫),SHANG GUAN Wen-Feng(上官文峰),et al.Chin.J.Catal.(Cuihua Xuebao),2006,27(9):767~771
  • 6ZHU Yong-Fa(朱永法),TAN Rui-Qin (谭瑞琴),FENG Jie (冯杰),et al.Chem.J.Chin.Univ.(Gaodeng Xuexiao Huaxue Xuebao),2000,21(11):1733-1737
  • 7JIA Li-Shan(贾立山),QIN Yong-Ning(秦永宁),MA Zhi (马智),et al.Chin.J.Catal.(Cuihua Xuebao),2004,25(1):19~22
  • 8CHEN Ming(陈敏),WANG Yoe-Wen(王幼文),ZHENG Xiao-Ming(郑小明).Chinese.J.Inorg.Chem.(Wuji Huaxue Xuebao),2003,19(10):1145~1148
  • 9Machida M,Ochiai K,Ito K.J.Catal.,2006,238:58-66
  • 10ZHAO Xiao-Ming(赵晓明),QIN Yong-Ning(秦永宁),MA Zhi(马智).Chem.Ind.Eng(Huaxue Gongye Yu Gongcheng),2004,21(5):34~33

同被引文献53

引证文献4

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部