Implications of Co-Feeding Water on the Growth Mechanisms of Retained Species on a SAPO-18 Catalyst during the Methanol-to-Olefins Reaction

被引:14
|
作者
Valecillos, Jose [1 ]
Hita, Idoia [2 ]
Sastre, Enrique [3 ]
Aguayo, Andres T. [1 ]
Castano, Pedro [1 ,2 ]
机构
[1] Univ Basque Country UPV EHU, Dept Chem Engn, POB 644, Bilbao 48080, Spain
[2] King Abdullah Univ Sci & Technol KAUST, KAUST Catalysis Ctr KCC, Multiscale React Engn, Thuwal 239556900, Saudi Arabia
[3] Inst Catalisis & Petr Quim CSIC, C Marie Curie 2, Madrid 28049, Spain
关键词
coke deactivation; high-resolution mass spectrometry; in-situ spectroscopy; methanol-to-hydrocarbons (MTH) reaction; SAPO-18 (AEI) zeolite; CARBON BOND FORMATION; PARTICLE SPECTROSCOPY; HYDROCARBONS REACTION; REACTION TEMPERATURE; MOLECULAR-SIEVES; CONVERSION; DEACTIVATION; ZEOLITE; TRANSFORMATION; SELECTIVITY;
D O I
10.1002/cctc.202100124
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
The dynamics of retained and deactivating species in a SAPO-18 catalyst during the methanol-to-olefins reaction have been followed using a combination of ex-situ and in-situ techniques in differential and integral reactors.The retained species were analyzed using extraction, in-situ FTIR and in-situ UV-vis spectroscopies combined with online product analysis (gas chromatography and mass spectrometry). The composition of the extracted soluble species was determined using gas chromatography-mass spectrometry and that of the insoluble species using high-resolution mass spectrometry. We observe a decrease in the formation and degradation rates of retained species when co-feeding water, whereas the extent of the decreases is the same across the entire spectrum of retained molecules. This indicates that co-feeding water unselectively quenches the formation of active and deactivating species. At the same time, the catalyst has an extended lifetime when co-feeding water due to the diffusion of species (particularly olefins) out of the SAPO-18 crystals, and subsequent growth of heavy polycyclic aromatic structures that imply less deactivation. These conclusions can be extrapolated to other MTO catalysts with relatively similar pore topology such as SAPO-34 or SSZ-13 structures.
引用
收藏
页码:3140 / 3154
页数:15
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