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首页|期刊导航|燃料化学学报(中英文)|不同孔结构CeTiOx催化剂的制备及其NH3-SCR脱硝性能研究

不同孔结构CeTiOx催化剂的制备及其NH3-SCR脱硝性能研究OACSTPCD

Preparation and NH3-SCR catalytic performance of CeTiOx catalysts with different pore structures

中文摘要英文摘要

为探究催化剂的孔结构对催化剂脱硝活性的影响,采用溶胶凝胶法分别制备了三维有序大孔-介孔(3DOM-m)CeTiOx、三维有序大孔(3DOM)CeTiOx、三维有序介孔(3DOm)CeTiOx,及无序孔(DM)CeTiOx,等四种不同孔结构的催化剂.NH3-SCR 测试结果表明,催化剂活性依次为 3DOM-m CeTiOx>3DOm CeTiOx,>3DOM CeTiOx>DM CeTiOx,3DOM-m CeTiOx表现出更优异的催化活性,NO转化率在60000h-1、250-400℃时超过90%.通过XRD、SEM、BET、NH3-TPD、in-situ DRIFTS等技术对催化剂进行表征分析.结果表明,催化剂的比表面积并不是决定CeTiOx脱硝活性的主导因素.3DOM-m CeTiOx,具有高度有序的大孔-介孔结构、丰富的Brønsted酸酸性位点,进而提高了催化剂的脱硝活性.3DOM-m CeTiOx催化剂在NH3-SCR反应过程中同时遵循E-R机理和L-H机理.

To investigate the influence of pore structure on the catalytic activity of catalysts,four catalysts including three-dimensionally ordered macroporous-mesoporous(3DOM-m)CeTiOx,three-dimensionally ordered macroporous(3DOM)CeTiOx,three-dimensionally ordered mesoporous(3DOm)CeTiOx and disordered mesoporous(DM)CeTiOx were synthesized by the sol-gel method.The NH3-SCR denitration testing results show that the performance of the catalysts with different pore structures follows the sequence of 3DOM-m CeTiOx>3DOm CeTiOx>3DOM CeTiOx>DM CeTiOx,and the 3DOM-m CeTiOx shows an excellent catalytic activity,with more than 90% NO conversion in the range of 250-400 ℃ at a GHSV of 60000 h-1.The characterization of catalysts by XRD,SEM,BET,NH3-TPD and in-situ DRIFTS indicates that the surface area is not the dominant factor determining the catalytic activity of CeTiOx.3DOM-m CeTiOx has a highly ordered macroporous-mesoporous structure and abundant Bronsted acidic sites,thereby improving the denitrification activity.The NH3-SCR reaction over the 3DOM-m CeTiOx mainly follows the L-H and E-R mechanisms.

谭晨晨;韩宇轩;胡亚琴;沈凯;丁世鹏;张亚平

东南大学 能源与环境学院能源热转换及其过程测控教育部重点实验室,江苏南京 210096

化学

CeTiOx三维有序大孔有序介孔NH3-SCR脱硝

CeTiOx3DOM structureordered mesoporous structureNH3-SCR

《燃料化学学报(中英文)》 2024 (001)

65-75 / 11

The project was supported by National Key Research and Development Program of China(2021YFB3500604).国家重点研发计划(2021YFB3500604)项目资助

10.1016/S1872-5813(23)60369-X

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