Biomass gasification is one of the most promising routes to produce green hydrogen, power, fuels, and chemicals, which has drawn much attention as the world moves away from fossil fuels. Syngas produced from gasification needs to go through an essential gas cleanup step for the removal of tars and particulates for further processing, which is one of the cost-inducing steps. Existing hot gas cleanup strategies involve the particulate removal step followed by catalytic tar reforming, which could be integrated into a single unit operation using porous ceramics owing to their advantages including high-temperature resistance, high corrosion resistance, flexibility, and robust mechanical integrity. Ceramic filters have proven to be effective at filtering particulates from hot gas streams in various applications including combustion, incineration, gasification, and pyrolysis. These materials have also been evaluated and used to an extent as catalyst support to remove contaminants such as nitrogen oxides (NO_x), volatile organic compounds (VOC), and in particular, tars, however, the use of these ceramic materials to remove both tars and particulates in one unit has not received much attention, although it has a promising potential to be a cost-effective hot gas cleanup strategy. Thus, this review presents the ability of catalytic ceramic filters to boost energy efficiency by converting unwanted byproducts while simultaneously eliminating PM in a single unit and is shown to be valuable in industrial processes across the board. This article presents a comprehensive and systematic overview and current state of knowledge of the use of porous ceramics for catalytic hot gas filtration applications with an emphasis on biomass syngas cleanup. In addition, a similar strategy for other applications such as combustion exhaust streams is presented. Prospects and challenges of taking this approach, and the necessary research and development to advance the novel use of reactive ceramic filters within biomass-fed thermal systems are presented. Major challenges include the low surface area of the ceramic filter media and high-pressure drop across the filter media, which can be overcome by wash coating or dip coating mechanisms and porosity tailored to meet the requirements. Owing to limited R&D efforts in this area, a systematic approach toward developing these integrated hot gas filtration systems is much needed, which will ultimately contribute to cost-effective green hydrogen production.

Amongst the issues associated with the commercialization of biomass gasification, the presence of tars has been one of the most difficult aspects to address. Tars are an impurity generated from the gasifier and upon their condensation cause problems in downstream equipment including plugging, blockages, corrosion, and major catalyst deactivation. These problems lead to losses of efficiency as well as potential maintenance issues resulting from damaged processing units. Therefore, the removal of tars is necessary in order for the effective operation of a biomass gasification facility for the production of high-value fuel gas. The catalytic activity of montmorillonite and montmorillonite-supported nickel as tar removal catalysts will be investigated in this study. Ni-montmorillonite catalyst was prepared, characterized, and tested in a laboratory-scale reactor for its efficiency in reforming tars using naphthalene as a tar model compound. Efficacy of montmorillonite-supported nickel catalyst was tested as a function of nickel content, reaction temperature, steam-to-carbon ratio, and naphthalene loading. The results demonstrate that montmorillonite is catalytically active in removing naphthalene. Ni-montmorillonite had high activity towards naphthalene removal via steam reforming, with removal efficiencies greater than 99%. The activation energy was calculated for Ni-montmorillonite assuming first-order kinetics and was found to be 84.5 kJ/mole in accordance with the literature. Long-term activity tests were also conducted and showed that the catalyst was active with naphthalene removal efficiencies greater than 95% maintained over a 97-h test period. A little loss of activity was observed with a removal decrease from 97% to 95%. To investigate the decrease in catalytic activity, characterization of fresh and used catalyst samples was performed using thermogravimetric analysis, transmission electron microscopy, X-ray diffraction, and surface area analysis. The loss in activity was attributed to a decrease in catalyst surface area caused by nickel sintering and coke formation.