Improving the low-temperature hydrothermal stability of Cu-SAPO-34 by the addition of Ag for ammonia selective catalytic reduction of NOx

被引:25
作者
Xiang, Xiao [1 ,2 ]
Cao, Yi [1 ]
Sun, Lijing [1 ,2 ]
Wu, Pengfei [1 ,2 ]
Cao, Lei [1 ]
Xu, Shutao [1 ]
Tian, Peng [1 ]
Liu, Zhongmin [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Natl Engn Lab Methanol Olefins, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Cu-SAPO-34; CuAg-SAPO-34; Hydrothermal stability; NH3-SCR; DIFFERENT FRAMEWORK TOPOLOGIES; ELECTRON-SPIN-RESONANCE; ADSORBATE INTERACTION; CU/SAPO-34; CATALYSTS; ECHO MODULATION; CU(II) LOCATION; COMBINED FTIR; NITRIC-OXIDE; SITU-DRIFTS; CU SITES;
D O I
10.1016/j.apcata.2017.12.001
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ag promoted Cu-SAPO-34 has been developed to improve the low-temperature hydrothermal stability of Cu-SAPO-34 for the NH3-SCR reaction. Kinetic tests show that the addition of Ag into Cu-SAPO-34 doesn't change the reaction mechanism. The ion-exchanged Ag species, which decrease the Bronsted acid density and provide more Lewis acid sites with moderate acidity, have a protective effect on the SAPO framework against low temperature steaming treatment (LTST). Higher surface Cu content is observed for CuAg2.25-SAPO-34, although CuAg2.23-SAPO-34 and Cu-SAPO-34 have similar content of isolated Cu ions. In situ DRIFTS studies demonstrate, for the first time, the NH3 molecules adsorbed on the weak/moderate acid sites (independent of the acid types such as Bronsted acid or Lewis acid) are more active than on the strong acid sites for the low-temperature SCR reaction. Compared with the original catalyst Cu-SAPO-34, the enhanced SCR activity of CuAg2.25-SAPO-34 after LTST is ascribed to the better preservation of total acid sites, higher moderate acid density (Lewis acid sites) and larger amount of surface Cu species on the CuAg2.25-SAPO-34 catalyst.
引用
收藏
页码:79 / 87
页数:9
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