摘要
通过柠檬酸络合法制得Ce0.75Cu0.25-x O2固溶体催化剂,采用X射线衍射、X射线光电子能谱和H2-程序升温还原对催化剂性能进行研究,考察催化剂对苯基挥发性有机物的催化燃烧活性。结果表明,催化剂中大量CuO溶入CeO2晶格中形成Ce0.75Cu0.25-x O2固溶体,固溶体的形成削弱了催化剂中的Cu—O和Ce—O键,提高了相应氧化物的低温可还原性,也提高了催化剂表面活性氧物种含量,从而提高了催化剂上苯基挥发性有机物的催化燃烧活性。在反应温度250℃和275℃时,Ce0.75Cu0.25-x O2固溶体催化剂上甲苯和二甲苯的催化燃烧转化率分别为97.6%和95.0%。Ce0.75Cu0.25-x O2催化剂上苯在280℃时催化燃烧转化率仅为61.0%,这可归因于苯分子稳定的芳香环结构不易被破坏。
Ce0.75Cu0.25-xO2 Solid solution oxide catalyst was prepared by citric acid complexation method and characterized by XRD,XPS and H2-TPR.The catalytic combustion performance of Ce0.75Cu0.25-xO2 catalyst for phenyl volatile organic compounds (PVOCs-benzene,toluene,and xylene) was investigated.The results indicated that copper oxide dissolved in CeO2 crystal lattice to form Ce0.75 Cu0.25-xO2 solid solution catalyst.Cu-O and Ce-O chemical bonds were weakened because of the formation of the solid solution,which enhanced the low temperature reducibihty of the corresponding oxide,the contents of surface active oxygen species on Ce0.75 Cu0.25-x O2 catalyst and catalytic combustion activity of PVOCs.The catalytic combustion conversion of toluene and xylene on Ce0.75 Cu0.25-xO2 catalyst reached 97.6% and 95.0% at 250 ℃ and 275 ℃,respectively.The catalytic combustion conversion of benzene on Ce0.75Cu0.25-xO2 catalyst was only 61.0% at 280 ℃,which attributed to a highly stable aromatic ring structure of benzene molecules.
出处
《工业催化》
CAS
2014年第2期123-127,共5页
Industrial Catalysis
基金
重庆市科委自然科学基金计划资助项目(CSTC2011jjA2008)
重庆工商大学学生科技创新基金项目(133009)
"大气环境模拟与污染控制"四川省高校重点实验室开放课题(KFKT201304)