汕头大学学报:自然科学版
汕頭大學學報:自然科學版
산두대학학보:자연과학판
Journal of Shantou University(Natural Science Edition)
2012年
1期
42-51
,共10页
Cu%Ca%Mn%Ce%共沉淀法
Cu%Ca%Mn%Ce%共沉澱法
Cu%Ca%Mn%Ce%공침정법
Cu%Ca%Mn%Ce%co-precipitation
采用共沉淀法制备CexMn1-xCaO2-λ载体,然后用等体积浸渍法负载活性组分Cu,制得Cuy/CexMn1-xCa2O2-λ催化剂.实验结果表明:Ce:Mn:Ca摩尔比为0.6:0.4:0.08.Cu负载量为5%时,制得的Cu5%/Ce0.6Mn0.4Ca0.6Ca0.08O2-λ催化剂对CO、C3H6和NO的转化反应具有良好的催化活性,能使CO、C3H6和NO的起燃温度‰分别为107℃、218℃和212℃.完全转化温度T90分别为144℃、323℃和298℃:南于Mn和Ca能与Ce氧化物形成稳定的立方品同溶体,不出现Mn2O3或CuO品相在载体表面富集的现象,Mn和Ca与Ce的良好协同作用有效提高催化活性,所以Cu5%/Ce0.6Mn0.4CaO0.08O2-λ催化性能良好.
採用共沉澱法製備CexMn1-xCaO2-λ載體,然後用等體積浸漬法負載活性組分Cu,製得Cuy/CexMn1-xCa2O2-λ催化劑.實驗結果錶明:Ce:Mn:Ca摩爾比為0.6:0.4:0.08.Cu負載量為5%時,製得的Cu5%/Ce0.6Mn0.4Ca0.6Ca0.08O2-λ催化劑對CO、C3H6和NO的轉化反應具有良好的催化活性,能使CO、C3H6和NO的起燃溫度‰分彆為107℃、218℃和212℃.完全轉化溫度T90分彆為144℃、323℃和298℃:南于Mn和Ca能與Ce氧化物形成穩定的立方品同溶體,不齣現Mn2O3或CuO品相在載體錶麵富集的現象,Mn和Ca與Ce的良好協同作用有效提高催化活性,所以Cu5%/Ce0.6Mn0.4CaO0.08O2-λ催化性能良好.
채용공침정법제비CexMn1-xCaO2-λ재체,연후용등체적침지법부재활성조분Cu,제득Cuy/CexMn1-xCa2O2-λ최화제.실험결과표명:Ce:Mn:Ca마이비위0.6:0.4:0.08.Cu부재량위5%시,제득적Cu5%/Ce0.6Mn0.4Ca0.6Ca0.08O2-λ최화제대CO、C3H6화NO적전화반응구유량호적최화활성,능사CO、C3H6화NO적기연온도‰분별위107℃、218℃화212℃.완전전화온도T90분별위144℃、323℃화298℃:남우Mn화Ca능여Ce양화물형성은정적립방품동용체,불출현Mn2O3혹CuO품상재재체표면부집적현상,Mn화Ca여Ce적량호협동작용유효제고최화활성,소이Cu5%/Ce0.6Mn0.4CaO0.08O2-λ최화성능량호.
The CexMn1-xCaO2-λ supporter was prepared by coprecipitation method, and then the Cuy/CexMn1-xCaO2-λcatalyst was made by volumetric immersion method to load active component Cu on the supporter. The experimental result indicated that when Ce: Mn : Ca molar ratio was 0.6:0.4 : 0.08 and the content of Cu was 5%(weigh), the Cu5%/Ce0.6Mn0.4Ca0.08O2-λ
catalyst showed high catalytic performance. The hght-off temperatures of CO, C3H6 and NO were 107 ℃, 218 ℃ and 212 ℃respectively, and CO, C3H6 and NO could be completely converted when the temperature were 144 ℃, 323 ℃ and 298 ℃respectively. Because Mn and Ca could form stable cubic structure of the solid solution with Ce oxide, and did not appear the Mn2O3 or CuO crystalline phase enrichment on the surface of the supporter, the good synergistic effect of Ce-Mn-Ca could improve the catalytic activity effectively, so the Cu5%/Ce0.6Mn0.4Ca0.08O2-λ catalyst exhibited high catalytic performance.