373,559 research outputs found

    Autocatalytic Pyrolysis of Wastewater Biosolids for Product Upgrading

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    The main goals for sustainable water resource recovery include maximizing energy generation, minimizing adverse environmental impacts, and recovering beneficial resources. Wastewater biosolids pyrolysis is a promising technology that could help facilities reach these goals because it produces biochar that is a valuable soil amendment as well as bio-oil and pyrolysis gas (py-gas) that can be used for energy. The raw bio-oil, however, is corrosive; therefore, employing it as fuel is challenging using standard equipment. A novel pyrolysis process using wastewater biosolids-derived biochar (WB-biochar) as a catalyst was investigated to decrease bio-oil and increase py-gas yield for easier energy recovery. WB-biochar catalyst increased the py-gas yield nearly 2-fold, while decreasing bio-oil production. The catalyzed bio-oil also contained fewer constituents based on GC-MS and GC-FID analyses. The energy shifted from bio-oil to py-gas, indicating the potential for easier on-site energy recovery using the relatively clean py-gas. The metals contained in wastewater biosolids played an important role in upgrading pyrolysis products. The Ca and Fe in WB-biochar reduced bio-oil yield and increased py-gas yield. The py-gas energy increase may be especially useful at water resource recovery facilities that already combust anaerobic digester biogas for energy since it may be possible to blend biogas and py-gas for combined use

    Economic tradeoff between biochar and bio-oil production via pyrolysis

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    This paper examines some of the economic tradeoffs in the joint production of biochar and bio-oil from cellulosic biomass. The pyrolysis process can be performed with different final temperatures, and with different heating rates. While most carbonization technologies operating at low heating rates result in higher yields of charcoal, fast pyrolysis is the technology of choice to produce bio-oils. Varying operational and design parameters can change the relative quantity and quality of biochar and bio-oil produced for a given feedstock. These changes in quantity and quality of both products affect the potential revenue from their production and sale. We estimate quadratic production functions for biochar and bio-oil. The results are then used to calculate a product transformation curve that characterizes the yields of bio-oil and biochar that can be produced for a given amount of feedstock, movement along the curve corresponds to changes in temperatures, and it can be used to infer optimal pyrolysis temperature settings for a given ratio of biochar and bio-oil prices.biochar, bio-oil, pyrolysis, biomass conversion, economic tradeoff

    Biocrude production by hydrothermal liquefaction of olive residue

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    Hydrothermal liquefaction (HTL) converts biomass into a crude bio-oil by thermally and hydrolytically decomposing the biomacromolecules into smaller compounds. The crude bio-oil, or biocrude, is an energy dense product that can potentially be used as a substitute for petroleum crudes. Liquefaction also produces gases, solids, and water-soluble compounds that can be converted to obtain valuable chemical species or can be used as energy vectors. The process is usually performed in water at 250°C-370°C and under pressures of 4-22 MPa: depending on the adopted pressure and temperature the process can be carried out in sub-critical or super-critical conditions. In the conditions reached in hydrothermal reactors, water changes its properties and acts as a catalyst for the biomass decomposition reactions. One of the main advantages of this process is that the energy expensive biomass-drying step, required in all the thermochemical processes, is not necessary, allowing the use of biomass with high moisture content such as microalgae or olive residue and grape mark. In this work, the feasibility of a hydrothermal process conducted under sub-critical conditions to obtain a bio-oil from the residue of olive oil production is investigated. The experimental tests were performed at 320°C and about 13 MPa, using a biomass to water weight ratio of 1:5. The influence of two different catalysts on the bio-oil yield and quality was investigated: CaO and a zeolite (faujasite-Na). CaO allows the increase of bio-oil yields, while the selected zeolite enhances the deoxygenation reactions, thus improving the bio-oil quality in terms of heating value

    Microwave pyrolysis of oil palm fibres

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    Malaysia and Indonesia are generating millions of ton of oil palm fibres (OPF) from their oil palm mills as biomass solid wastes which needs proper waste utilization application. The main purpose of the present research was to pyrolyse the OPF biomass into bio-oil using microwave irradiation technique. A domestic microwave of 1000 W and 2.45 GHz frequency was modified to accommodate fluidized bed system. It was found that OPF showed poor microwave absorbing characteristics. Therefore, an appropriate microwave-absorbing material such as biomass char was added to initiate the pyrolysis process. Temperature profiles and bio-oil yield was investigated by varying the ratio of OPF to microwave absorber. It was found that the yield of bio-oil depended on the ratio of OPF to microwave absorber. Particular attention on the temperature profiles was also taken into account during microwave heating of OPF. It can be concluded that microwave technique can save significant time and energy through its rapid and volumetric heating characteristic

    Use of Desulfovibrio and Escherichia coli Pd-nanocatalysts in reduction of Cr(VI) and hydrogenolytic dehalogenation of polychlorinated biphenyls and used transformer oil

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    BACKGROUND Desulfovibrio spp. biofabricate metallic nanoparticles (e.g. ‘Bio-Pd’) which catalyse the reduction of Cr(VI) to Cr(III) and dehalogenate polychlorinated biphenyls (PCBs). Desulfovibrio spp. are anaerobic and produce H2S, a potent catalyst poison, whereas Escherichia coli can be pre-grown aerobically to high density, has well defined molecular tools, and also makes catalytically-active ‘Bio-Pd’. The first aim was to compare ‘Bio-Pd’ catalysts made by Desulfovibrio spp. and E. coli using suspended and immobilised catalysts. The second aim was to evaluate the potential for Bio-Pd-mediated dehalogenation of PCBs in used transformer oils, which preclude recovery and re-use.\ud RESULTS Catalysis via Bio-PdD. desulfuricans and Bio-PdE. coli was compared at a mass loading of Pd:biomass of 1:3 via reduction of Cr(VI) in aqueous solution (immobilised catalyst) and hydrogenolytic release of Cl- from PCBs and used transformer oil (catalyst suspensions). In both cases Bio-PdD. desulfuricans outperformed Bio-Pd E. coli by ~3.5-fold, attributable to a ~3.5-fold difference in their Pd-nanoparticle surface areas determined by magnetic measurements (Bio-PdD. desulfuricans) and by chemisorption analysis (Bio-PdE. coli). Small Pd particles were confirmed on D. desulfuricans and fewer, larger ones on E. coli via electron microscopy. Bio-PdD. desulfuricans-mediated chloride release from used transformer oil (5.6 ±\pm 0.8 ÎŒ\mug mL-1 ) was comparable to that observed using several PCB reference materials. \ud CONCLUSIONS At a loading of 1:3 Pd: biomass Bio-PdD. desulfuricans is 3.5-fold more active than Bio-PdE. coli, attributable to the relative catalyst surface areas reflected in the smaller nanoparticle sizes of the former. This study also shows the potential of Bio-PdD. desulfuricans to remediate used transformer oil

    Upgrading Crude Bio-Oil (CBO) dari Biomassa Menjadi Upgrade Bio-Oil (UBO) dengan Katalis Ni/Lempung

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    Objective of this research is to upgrade quality of bio-oil product from biomass of acacia. In this study several parameters were determined such us determine the effect of temperature reaction and ethanol : bio-oil ratio. And then compared physical and chemical characteristic of crude bio-oil (CBO) to upgraded bio-oil (UBO). In upgrading process, mixture of bio-oil and ethanol 36 gram, Ni/clay catalyst 0,3 gram, with variation of ethanol : bio-oil ratio are 5:1 (30 gram ethanol : 6 gram bio-oil), 3:1 (27:9) , 2:1 (24:12) and 1:1 (18:18) as well as temperature reaction variations are 60, 70 and 80 oC. The highest result on bio-oil yields 1:1 ratio and 60 oC was away 79,25% with calorific value increase from 3,784 into 18,339 MJ/kg. The dominant chemical components in crude bio-oil (CBO) such us aldehydes (58,91%), acids (13,43%) and esthers (12,26%) while in upgraded bio-oil (UBO) such us aldehydes (27,45%), phenols and furans (22,75%), alkanes and alkenes (19,48%), esthers (14,84%) and acids (1,53%) respectively

    Techno-economic performance analysis of biofuel production and miniature electric power generation from biomass fast pyrolysis and bio-oil upgrading

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    The techno-economic performance analysis of biofuel production and electric power generation from biomass fast pyrolysis and bio-oil hydroprocessing is explored through process simulation. In this work, a process model of 72 MT/day pine wood fast pyrolysis and bio-oil hydroprocessing plant was developed with rate based chemical reactions using Aspen Plus¼ process simulator. It was observed from simulation results that 1 kg s−1 pine wooddb generate 0.64 kg s−1 bio-oil, 0.22 kg s−1 gas and 0.14 kg s−1 char. Simulation results also show that the energy required for drying and fast pyrolysis operations can be provided from the combustion of pyrolysis by-products, mainly, char and non-condensable gas with sufficient residual energy for miniature electric power generation. The intermediate bio-oil product from the fast pyrolysis process is upgraded into gasoline and diesel via a two-stage hydrotreating process, which was implemented by a pseudo-first order reaction of lumped bio-oil species followed by the hydrocracking process in this work. Simulation results indicate that about 0.24 kg s−1 of gasoline and diesel range products and 96 W of electric power can be produced from 1 kg s−1 pine wooddb. The effect of initial biomass moisture content on the amount of electric power generated and the effect of biomass feed composition on product yields were also reported in this study. Aspen Process Economic Analyser¼ was used for equipment sizing and cost estimation for an nth plant and the product value was estimated from discounted cash flow analysis assuming the plant operates for 20 years at a 10% annual discount rate. Economic analysis indicates that the plant will require £16.6 million of capital investment and product value is estimated at £6.25/GGE. Furthermore, the effect of key process and economic parameters on product value and the impact of electric power generation equipment on capital cost and energy efficiency were also discussed in this study
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