Recent Progress to Understand and Improve Zeolite Stability in the Aqueous Medium

被引:34
作者
Prodinger, Sebastian [1 ]
Derewinski, Miroslaw A. [2 ,3 ]
机构
[1] Univ Delaware, Newark, DE 19711 USA
[2] Pacific Northwest Natl Lab, Inst Integrated Catalysis, Richland, WA 99352 USA
[3] Polish Acad Sci, Jerzy Haber Inst Catalysis & Surface Chem, PL-30239 Krakow, Poland
关键词
zeolite; stability; hot liquid water; deactivation; catalysis; HYDROTHERMAL STABILITY; SN-BETA; HYDROPHOBIC ZEOLITES; MOLECULAR-SIEVES; HIGH-SILICA; THERMAL-STABILITY; ACID CATALYSIS; BIOMASS; CONVERSION; PHASE;
D O I
10.1134/S0965544120040143
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The work reviewed here attempts to summarize the growing literature on zeolite stability in hot liquid water. This required to first establish the nature, structure and interactions of the active sites in Bronsted and Lewis acidic microporous materials in the presence of liquid water. This understanding was then transferred to zeolite stability and catalyst deactivation. While early results correctly established Si-O-Si hydrolysis as the dominant pathway compared to the Si-O-Al hydrolysis observed in steaming, it also focused extensively on the positive role of framework and extra-framework Al in stabilizing zeolites. However, stability was instead found to more directly correlate with the number of internal structural defects and intraporous water concentration. Stabilization protocols for Bronsted acidic zeolites are described in detail. In the case of Lewis acidic zeolites, their inherent hydrophobic behavior (Si/M >100) makes them more resistant towards water, however, issues such as reversible carbonaceous species formation as well as irreversible metal leaching and fouling remain. Finally, we summarize the most important factors in designing robust and efficient zeolite catalysts made to withstand hot liquid water.
引用
收藏
页码:420 / 436
页数:17
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