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Deactivation and regeneration of solid acid and base catalyst bodies used in cascade for bio-oil synthesis and upgrading

Authors :
Hernández-Giménez, Ana M.
Hernando, Héctor
Danisi, Rosa M.
Vogt, Eelco T.C.
Houben, Klaartje
Baldus, Marc
Serrano, David P.
Bruijnincx, Pieter C.A.
Weckhuysen, Bert M.
NMR Spectroscopy
Inorganic Chemistry and Catalysis
Organic Chemistry and Catalysis
Sub Inorganic Chemistry and Catalysis
Sub NMR Spectroscopy
Sub Organic Chemistry and Catalysis
NMR Spectroscopy
Inorganic Chemistry and Catalysis
Organic Chemistry and Catalysis
Sub Inorganic Chemistry and Catalysis
Sub NMR Spectroscopy
Sub Organic Chemistry and Catalysis
Source :
Journal of Catalysis, 405, 641-651, Journal of Catalysis, 405, 641. Academic Press Inc.
Publication Year :
2022
Publisher :
Elsevier, 2022.

Abstract

The modes of deactivation -and the extent to which their properties can be restored- of two catalyst bodies used in cascade for bio-oil synthesis have been studied. These catalysts include a solid acid granulate (namely ZrO2/desilicated zeolite ZSM-5/attapulgite clay) employed in ex-situ catalytic fast pyrolysis of biomass, and a base extrudate (K-exchanged zeolite USY/attapulgite clay) for the subsequent bio-oil upgrading. Post-mortem analyses of both catalyst bodies with Raman spectroscopy and confocal fluorescence microscopy revealed the presence of highly poly-aromatic coke distributed in an egg-shell manner. Deactivation due to coke adsorption onto acid sites affected the zeolite ZSM-5-based catalyst, while for the base catalyst it is structural integrity loss, resulting from KOH-mediated zeolite framework collapse, the main deactivating factor. A hydrothermal regeneration process reversed the detrimental effects of coke in the acid catalyst, largely recovering catalyst acidity (∼80%) and textural properties (∼90%), but worsened the structural damage suffered by the base catalyst.

Details

Language :
English
ISSN :
00219517 and 10902694
Database :
OpenAIRE
Journal :
Journal of Catalysis, 405, 641-651, Journal of Catalysis, 405, 641. Academic Press Inc.
Accession number :
edsair.doi.dedup.....96e1979b5228047a261c0d3f408aaf3f