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Continuous hydrothermal gasification of glycerol mixtures: Effect of glycerol and its degradation products on the continuous salt separation and the enhancing effect of K3PO4 on the glycerol degradation
Affiliation:1. Key Laboratory of Coal Processing and Efficient Utilization, Ministry of Education, China University of Mining & Technology, Xuzhou 221116, Jiangsu, China;2. The Gene and Linda Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, WA 99164, USA
Abstract:At the Paul Scherrer Institut (PSI) a continuous process for the catalytic hydrothermal gasification of wet biomass to synthetic natural gas (SNG) has been developed. The catalytic reactor is operated at temperatures of 400–450 °C and pressures of 25–30 MPa. Salts contained in the biomass and released during the liquefaction step are continuously withdrawn in the supercritical salt separation step and recovered as a concentrated brine upstream of the catalytic reactor. The recovered salts may be recycled as valuable nutrients or fertilizers after a certain work-up.Salt management was identified as critical issue in many different hydrothermal processes such as supercritical water oxidation (SCWO) and in catalyzed or non-catalyzed gasification technologies in near- and supercritical water. In this article we focus on the influence of organics, in this case glycerol and its hydrothermal degradation products, on the continuous salt separation performance. In the presence of organics higher temperatures are needed in the salt separator for an efficient salt separation and recovery due to a higher overall fluid density in the presence of glycerol compared to the density of pure water at the same conditions. Increasing temperatures in the salt separator lead to an increased degradation and, in particular, gasification of the glycerol. The salt studied, i.e. K3PO4, catalyzed the gasification of the glycerol to CO, H2, CO2, and CH4 as well as the water gas shift reaction. Due to the increased glycerol gasification at 460 °C in the salt separator, the fluid mixture density was lowered to similar values of pure water under the same conditions. Hence, at the fluid temperature of 460 °C in the salt separator the same salt separation performance was observed for water–K3PO4 and for an aqueous mixture of 20 wt.% glycerol with K3PO4.
Keywords:Supercritical water  Biomass  Glycerol  Hydrothermal gasification  Catalytic gasification  Autothermal operation  Salt separation  Salt recovery  Methane  Synthetic natural gas  SNG
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