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作 者:穆金城[1] 于海峰[1] 田维亮[1] 舒尊哲[1] 杨泽霞[1] 李秀敏[1] MU Jin-cheng YU Hai-feng TIAN Wei-liang SHU Zun-zhe YANG Ze-xia LI Xiu-min(Engineering Laboratory of Chemical Resources Utilization in South Xinjiang of XPCC/College of life Science, Tarim University, Xinfiang Alar , 843300, China)
机构地区:[1]塔里木大学生命科学学院兵团南疆化工资源利用工程实验室,新疆阿拉尔843300
出 处:《分子催化》2017年第1期92-100,共9页Journal of Molecular Catalysis(China)
基 金:北京化工大学化工资源有效利用国家重点实验室开放课题项目(CRE2013C304);塔里木大学校长基金项目(TDZKSS201418)~~
摘 要:采用不同方法、不同负载量、不同焙烧温度制备CeO_2改性的SiO_2-CuO-CeO_2复合氧化物催化剂,并对其进行X射线衍射分析、扫描式电子显微镜、TG-DSC、N_2吸附-脱附和H_2-TPR等表征.在温和条件(65℃、常压)下,以过氧化氢为氧化剂,乙腈为溶剂,苯并噻吩(BT)为模型硫化物,考察SiO_2-CuO-CeO_2复合氧化物催化剂的氧化脱硫性能,确定复合氧化物的最佳制备工艺条件.结果表明,适量的添加CeO_2可以提高CuO在SiO_2上的分散度、比表面积和孔径,提高复合氧化物的活性;溶胶-凝胶法制备的SiO_2-0.1CuO-0.02CeO_2复合氧化物,在500℃下焙烧,催化剂活性最高,脱硫率最高为81.6%.催化剂的重复使用5次,脱硫率仍可达到60.0%.CeO2 modified SiO2-CuO-CeO2 composite oxide catalysts were prepared by using different methods,different loadings,different calcination temperature. The catalysts were characterized by X-ray diffraction( XRD),scanning electron microscope( SEM),thermogravimetry and differential scanning calorimetry( TG-DSC),N2 adsorption-desorption and temperature-programmed reduction by H2( H2-TPR). Under mild conditions( 65 ℃,atmospheric pressure),the oxidative desulfurization performance of SiO2-CuO-CeO2 composite oxide catalysts were investigated under the condition of hydrogen peroxide as the oxidant,acetonitrile as a solvent,benzothiophene( BT) as a model sulfide. Finally,this paper established the best preparation conditions of the composite oxide. The results showed that the addition of appropriate amount of CeO2 into the catalyst increases the dispersion of CuO,the specific surface area,pore size and the activity of the complex oxide. The SiO2-0.1CuO-0.02 Ce O2 composite oxide were prepared by sol-gel method at calcination temperature of 500 ℃ had the highest activity,oxide desulfurization rate was 81.6%. After the catalyst was reused for five times,the desulfurization rate still reached 60.0%.
关 键 词:氧化脱硫 CeO2改性 SiO2-CuO-CeO2 复合氧化物 苯并噻吩
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