含氧预硫化掺杂Cu-LaCoO3催化剂上CO还原SO2催化反应研究
Study on the Catalytic Reduction of SO2 by CO and Sulfurization Process in the Presence of Oxygen over Doped Cu-LaCoO3 Catalysts
作者单位
王广建 天津大学化工学院天津 300072
青岛科技大学化工学院青岛 266042 
秦永宁 天津大学化工学院天津 300072 
马智 天津大学化工学院天津 300072 
齐晓周 天津大学化工学院天津 300072 
丁彤 天津大学化工学院天津 300072 
摘要: 
关键词: 二氧化硫  一氧化碳  钴酸镧  铜掺杂  
基金项目: 
Abstract: The LaCoO3 and 1%,10%,20%,30% doped Cu-LaCoO3 were prepared and studied. Two pretreated process were studied to investigate the effect of pretreating process of the catalysts on the reduction of SO2 by CO. One was using the mixture of SO2 and CO for catalysts sulfurized and poisoned in the presence of oxygen and the other was using SO2 and CO pre-reduced in the absence of oxygen. The evaluations were based on the SO2 conversion as well as sulfur selectivity and COS produced in a gradientless, quartz tubular packed-bed reactor. It was found that the catalysts sulfurized and poisoned under the mixture of SO2 and CO in the presence of oxygen could sustain its activity better than the pre-reduced catalysts. The activity decrease of the sulfurized and poisoned catalysts was very small after 4 h reaction. But for the two pre-reduced catalysts, SO2 conversion was only 17% over one 10% doped Cu-LaCoO3 and the other was deactivated after 140 min reaction. It was also found that all the doped Cu catalysts, sulfurized and poisoned in the presence of oxygen, presented higher oxygen resistance than the pre-reduced catalysts after reaction. The SO2 conversion of all the doped Cu catalysts decreased a little over 40 h reaction, while the activity of un-doped LaCoO3 was lowered to only 0.2 times of the initial activity. The other result showed that the COS formation was minimized in the doped Cu catalysts. From the results, it could be concluded that the 10% Cu-LaCoO3 was the most effective of the catalysts for removing sulfur with little COS formation.
Keywords: sulfur dioxide  carbon monoxide  lanthanum cobaltate  doped copper  oxygen
 
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王广建,秦永宁,马智,齐晓周,丁彤.含氧预硫化掺杂Cu-LaCoO3催化剂上CO还原SO2催化反应研究[J].无机化学学报,2006,22(3):571-576.
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