170 research outputs found

    Carbon Formation in the Reforming of Simulated Biomass Gasification Gas on Nickel and Rhodium Catalysts

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    Biomass gasification gas contains hydrocarbons that must be converted to CO and H2 prior to the utilization of the gas in a synthesis unit. Autothermal or steam reforming operating with a nickel or noble metal catalyst is a feasible option to treat the gas, but the harsh reaction conditions may lead to the formation of solid carbon. This study discusses the effects of pressure, time-on-stream, and ethylene content on the carbon formation on nickel and rhodium catalysts. The experiments were carried out with laboratory-scale equipment using reaction conditions that were closely simulated after a pilot-scale biomass gasifier. The results indicated that ethylene content above 20,000 vol-ppm and the increased pressure would increase the carbon formation, although there were differences between the rhodium and nickel catalysts. However, carbon formation was significantly more pronounced on the nickel catalyst when the reaction time was increased from 5 h to 144 h. The type of carbon was found to be primarily encapsulating and graphitic. The formation of whisker carbons (also known as carbon nanotubes) was not observed, which is consistent with the literature as the feed gas contained H2S. It was concluded that utilizing a noble metal catalyst as the front layer of the catalyst bed could lower the risk for carbon formation sufficiently to provide stable long-term operation

    Activated Carbons for Syngas Desulfurization:Evaluating Approaches for Enhancing Low-Temperature H<sub>2</sub>S Oxidation Rate

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    Scientific paper based on the research work of VTT and, specifically, on the syngas desulfurization treatment with activated carbons. In BioSFerA, VTT is in charge of the gasification process of the selected feedstocks and its scale-up into a pilot process, where the gasification and fermentation units are integrated

    Pure aromatics from biomass

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    Atomic Layer Deposition Coated Filters in Catalytic Filtration of Gasification Gas

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    Steel filter discs were catalytically activated by ALD, using a coating of supporting Al2O3 layer and an active NiO layer for gas cleaning. Prepared discs were tested for model biomass gasification and gas catalytic filtration to reduce or eliminate the need for a separate reforming unit for gasification gas tars and lighter hydrocarbons. Two different coating methods were tested. The method utilizing the stop-flow setting was shown to be the most suitable for the preparation of active and durable catalytic filters, which significantly decreases the amount of tar compounds in gasification gas. A pressure of 5 bar and temperatures of over 850 °C are required for efficient tar reforming. In optimal conditions, applying catalytic coating to the filter resulted in a seven-fold naphthalene conversion increase from 7% to 49%

    Atomic Layer Deposition Coated Filters in Catalytic Filtration of Gasification Gas

    Get PDF
    Steel filter discs were catalytically activated by ALD, using a coating of supporting Al2O3 layer and an active NiO layer for gas cleaning. Prepared discs were tested for model biomass gasification and gas catalytic filtration to reduce or eliminate the need for a separate reforming unit for gasification gas tars and lighter hydrocarbons. Two different coating methods were tested. The method utilizing the stop-flow setting was shown to be the most suitable for the preparation of active and durable catalytic filters, which significantly decreases the amount of tar compounds in gasification gas. A pressure of 5 bar and temperatures of over 850 °C are required for efficient tar reforming. In optimal conditions, applying catalytic coating to the filter resulted in a seven-fold naphthalene conversion increase from 7% to 49%

    Molecular Layer Deposition Using Ring-Opening Reactions : Molecular Modeling of the Film Growth and the Effects of Hydrogen Peroxide

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    Published under an ACS AuthorChoice licenseNovel coating materials are constantly needed for current and future applications in the area of microelectronics, biocompatible materials, and energy-related devices. Molecular layer deposition (MLD) is answering this cry and is an increasingly important coating method for organic and hybrid organic-inorganic thin films. In this study, we have focused on hybrid inorganic-organic coatings, based on trimethylaluminum, monofunctional aromatic precursors, and ring-opening reactions with ozone. We present the MLD processes, where the films are produced with trimethylaluminum, one of the three aromatic precursors (phenol, 3-(trifluoromethyl) phenol, and 2-fluoro-4-(trifluoromethyl)benzaldehyde), ozone, and the fourth precursor, hydrogen peroxide. According to the in situ Fourier-transform infrared spectroscopy measurements, the hydrogen peroxide reacts with the surface carboxylic acid group, forming a peroxyacid structure (C(O)-O-OH), in the case of all three processes. In addition, molecular modeling for the processes with three different aromatic precursors was carried out. When combining these modeling results with the experimental research data, new interesting aspects of the film growth, reactions, and properties are exploited.Peer reviewe

    Hydrogen release from liquid organic hydrogen carriers catalysed by platinum on rutile-anatase structured titania

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    A liquid organic hydrogen carrier (LOHC) is an interesting concept for hydrogen storage. We describe herein a new, active catalyst system for dehydrogenation of perhydrogenated dibenzyl toluene (H18-DBT), which is a promising LOHC candidate. Pt supported on a rutile-anatase form of titania was found to be more active than Pt supported on anatase-only titania, or on alumina, and almost equally active as Pt supported on carbon. Robust and durable metal oxide supports are preferred for catalysing reactions at high temperatures.Peer reviewe

    Longitudinal Pattern of First-Phase Insulin Response Is Associated With Genetic Variants Outside the Class II HLA Region in Children With Multiple Autoantibodies

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    A declining first-phase insulin response (FPIR) is associated with positivity for multiple islet autoantibodies, irrespective of class II HLA DR-DQ genotype. We examined the associations of FPIR with genetic variants outside the HLA DR-DQ region in the Finnish Type 1 Diabetes Prediction and Prevention (DIPP) study in children with and without multiple autoantibodies. Association between FPIR and class I alleles A*24 and B*39 and eight single nucleotide polymorphisms outside the HLA region were analyzed in 438 children who had one or more FPIR results available after seroconversion. Hierarchical linear mixed models were used to analyze repeated measurements of FPIR. In children with multiple autoantibodies, the change in FPIR over time was significantly different between those with various PTPN2 (rs45450798), FUT2 (rs601338), CTSH (rs3825932), and IKZF4 (rs1701704) genotypes in at least one of the models. In general, children carrying susceptibility alleles for type 1 diabetes experienced a more rapid decline in insulin secretion compared with children without susceptibility alleles. The presence of the class I HLA A*24 allele was also associated with a steeper decline of FPIR over time in children with multiple autoantibodies. Certain genetic variants outside the class II HLA region may have a significant impact on the longitudinal pattern of FPIR.Peer reviewe
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