热液循环
吸附
魔角纺纱
解吸
傅里叶变换红外光谱
材料科学
水解
离子
红外光谱学
漫反射红外傅里叶变换
核磁共振波谱
分析化学(期刊)
催化作用
化学
物理化学
化学工程
立体化学
光催化
有机化学
工程类
作者
Yue Ma,Yang Gao,Xiaodong Wu,Baofang Jin,Rui Ran,Zhichun Si,Duan Weng
标识
DOI:10.1021/acsami.2c13890
摘要
The influences of gaseous, weakly adsorbed, and strongly adsorbed NH 3 on the low-temperature (<100 °C) hydrothermal stability of SAPO-34 and Cu-SAPO-34 were investigated. NH 3 temperature-programmed desorption (NH 3 -TPD), 1 H magic angle spinning nuclear magnetic resonance (MAS NMR), and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) were adopted to characterize the adsorption states of NH 3 and H 2 O in SAPO-34, and the destruction of the SAPO-34 framework was revealed by direct and cross-polarization 29 Si, 27 Al, and 31 P MAS NMR. Gaseous NH 3 coadsorbed with H 2 O inside SAPO-34 micropores and induced the hydrolysis of framework P–O–Al and Si–O(H)–Al bonds. Weakly adsorbed NH 3 was released during aging and played a similar negative role to gaseous NH 3 . When being combined with hydrolyzed Al species from the framework, active Cu ions transformed to inactive CuAl 2 O 4 -like species, leading to deactivation in low-temperature SCR of Cu-SAPO-34. Strongly adsorbed NH 4 + via 200 °C preadsorption protected the framework integrity of SAPO-34 and the SCR activity of Cu-SAPO-34.
科研通智能强力驱动
Strongly Powered by AbleSci AI