Catalytic Tar Conversion in Two Different Hot Syngas Cleaning Systems

Tar in the product gas of biomass gasifiers reduces the efficiency of gasification processes and causes fouling of system components and pipework. Therefore, an efficient tar conversion in the product gas is a key step of effective and reliable syngas production. One of the most promising approaches...

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Bibliographic Details
Main Authors: Grazyna Straczewski, Robert Mai, Uta Gerhards, Krassimir Garbev, Hans Leibold
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Series:Catalysts
Subjects:
Online Access:https://www.mdpi.com/2073-4344/11/10/1231
Description
Summary:Tar in the product gas of biomass gasifiers reduces the efficiency of gasification processes and causes fouling of system components and pipework. Therefore, an efficient tar conversion in the product gas is a key step of effective and reliable syngas production. One of the most promising approaches is the catalytic decomposition of the tar species combined with hot syngas cleaning. The catalyst must be able to convert tar components in the synthesis gas at temperatures of around 700 °C downstream of the gasifier without preheating. A Ni-based doped catalyst with high activity in tar conversion was developed and characterized in detail. An appropriate composition of transition metals was applied to minimize catalyst coking. Precious metals (Pt, Pd, Rh, or a combination of two of them) were added to the catalyst in small quantities. Depending on the hot gas cleaning system used, both transition metals and precious metals were co-impregnated on pellets or on a ceramic filter material. In the case of a pelletized-type catalyst, the hot gas cleaning system revealed a conversion above 80% for 70 and 110 h. The catalyst composed of Ni, Fe, and Cr oxides, promoted with Pt and impregnated on a ceramic fiber filter composed of Al<sub>2</sub>O<sub>3</sub>(44%)/SiO<sub>2</sub>(56%), was the most active catalyst for a compact cleaning system. This catalyst was catalytically active with a naphthalene conversion of around 93% over 95 h without catalyst deactivation.
ISSN:2073-4344