The objective of this thesis is to experimentally investigate the performance of steam gasification of chars of pure coal (lignite, sub-bituminous), pure biomass (radiata pine, eucalyptus nitens) and their blends. The influences of gasification temperature, types of coal and biomass, coal-biomass blending ratio, alkali and alkaline earth metal (AAEM) in lignite, on specific gasification characteristics (producer gas composition and yield, char reactivity) were studied. In addition, synergistic effects in co-gasification of coal-biomass blend char were also investigated. This project is in accordance with objectives of the BISGAS Consortium. In this study, experiments were performed in a bench-scale gasifier at gasification temperatures of 850°C, 900°C and 950°C, respectively. Two types of coals (lignite and sub-bituminous) and two kinds of biomass (radiata pine and eucalyptus nitens) from New Zealand were selected as sample fuels. From these raw materials, the chars with coal-to-biomass blending ratios of 0:100 (pure coal), 20:80, 50:50, 80:20 and 100:0 (pure biomass), which were derived through the devolatilization at temperature of 900°C for 7 minutes, were gasified with steam as gasification agent. During the gasification tests, the producer gas composition and gas production were continuously analysed using a Micro gas chromatograph. When the gas production was undetectable, the gasification process was assumed to be completed and the gasification time was recorded. The gasification producer gas consisted of three main gas components: hydrogen (H2), carbon monoxide (CO) and carbon dioxide (CO2). The results from gasification of chars of individual solid fuels (coal or biomass) confirmed that biomass char gasification was faster than coal char gasification. The influences of gasification temperatures were shown as: when gasification temperature increased, the H2 yield increased in coal char gasification but decreased in biomass char gasification. In the meantime, CO yields increased while CO2 yields decreased in both coal char and biomass char gasification. In addition, the char reactivity of all the pure fuel samples increased with elevated gasification temperatures. The results from co-gasification of coal-biomass blend char exhibited that the syngas production rate, which is defined as the total gas production divided by the gasification completion time, was enhanced by an increase in gasification temperatures as well as an increase in the biomass proportion in the blend. The AAEM species played a significant catalytic role in both gasification of pure coal chars and co-gasification of coal-biomass blend chars. The presence of AAEM increased the producer gas yield and enhanced the char reactivity. The positive synergistic effects of the coal-biomass blending char on syngas production rate only existed in the co-gasification of lignite-eucalyptus nitens blend chars. The other blend chars showed either insignificant synergistic effects or negative effects on the syngas production rate.

This research forms part of a programme of work at the University of Canterbury investigating the production of liquid fuels from biomass. The drivers for this research are the plentiful supply of woody biomass in New Zealand as well as the necessity for a reduction in the use of fossil fuels. Fischer-Tropsch synthesis has been chosen as the base conversion method for syngas to liquid fuels. While Fischer-Tropsch plants are traditionally very large, the low geographical density of the biomass feedstock necessitates a shift from a traditional economies of scale approach. In this research a sawmill integrated polygeneration scenario is proposed that recognises the synergy between the heat and electrical requirements of a mill and the Fischer-Tropsch process that can supply both as well as liquid fuels. Techno-economic modelling of variations to this polygeneration arrangement were performed using a traditional Fischer-Tropsch slurry reactor as the basis. The breakeven price of syncrude produced in the process based on a 30 year plant life and 10% discount factor was as low as $US 167 per barrel. This arrangement is coupled with development of and experimentation with a microchannel reactor in a further attempt to overcome economies of scale disadvantages. The lab scale microchannel reactor consisted of a shim with 50 channels of 37mm length with 0.2mm height and 0.3mm width. The microchannel reactor was tested with shorter run periods to compare different catalyst washcoats consisting of neat cobalt, cobalt on titania and a combustion synthesis method over a temperature range of 210-240°C at 20 bar. Comparison was also made to a lab scale fixed bed reactor with a powdered cobalt on titania catalyst. The neat cobalt washcoat proved to have the best performance per unit mass of catalyst of the three washcoats. The performance of the microchannel reactor was 32-40 times better per unit catalyst mass than the fixed bed reactor. From data based on the shorter runs the neat cobalt washcoat and the cobalt on titania washcoat were selected for further analysis over longer runs at a range of pressures from 2-20 bar and temperatures from 210-240°C. These runs were each approximately 70 hours long and provided a better analysis of the narrowed catalyst choice. The productivity results of the catalysts were fitted to established kinetic equations from literature with an excellent correlation. More accurate Anderson-Schultz-Flory selectivity values were also obtained ranging between 0.72 to 0.82. This is certainly an area that would warrant further attention as a higher selectivity has a very positive affect on plant economics. Establishment of the kinetic equations for the catalyst performance allowed modelling of reactors with greater volume along with investigation of mass transfer limitations to assist in scale up of the technology. It was found that under 4-5mm hydraulic diameter channel dimensions the mass transfer limitation from the bulk gas phase to the catalyst interface is negligible. A scaled up microchannel reactor concept design is proposed utilising stainless steel mesh folded into 2mm channels to increase catalyst surface area compared to straight shim. A costing correlation was produced per unit of reactor volume to allow a full scale cost of the microchannel reactor to be estimated for inclusion into the techno-economic model. The revised techno-economic model was optimised through pressure variation to give a breakeven syncrude value of $US118 per barrel at Fischer-Tropsch reaction conditions of 10 bar and 240°C. This brings the value well within historical crude price trends.

No description available.

No description available.

No description available.

No description available.

No description available.

No description available.

No description available.

Mozambique has vast forestry resources and also considerable biomass waste material such as bagasse, rice husks, sawdust, coconut husks and shells, cashew nut shell and lump charcoal waste. The potential of the total residues from the agricultural sector and the forest industry is estimated to be approximately 13 PJ. This amount of energy covers totally the production of charcoal which amounted to approximately 12.7 PJ in 2006. Although biomass is an attractive renewable source of energy, it is generally difficult to handle, transport, storage and use due to its lower homogeneity, its lower energy density and the presence of non-combustible inorganic constituents, which leads to different problems in energy conversion units such as deposition, sintering, agglomeration, fouling and corrosion. Therefore, a pretreatment of the biomass to solve these problems could lead to a change of current biomass utilization situation. The aim of this study is to convert Mozambican woody biomass residue into a solid biochar that resembles low-grade coal. In this work the current energy situation in Mozambique has been reviewed, and the available and potential renewable sources including residues from agricultural crops and forest industry as energy have been assessed. It was found that the country is endowed with great potential for biofuel, solar, hydro and wind energy production. However, the production today is still far from fulfilling the energy needs of the country, and the majority of people are still not benefiting from these resources. Charcoal and firewood are still the main sources of energy and will continue to play a very important role in the near future. Additionally, enormous amounts of energy resources are wasted, especially in the agricultural sector. These residues are not visible on national energy statistics. The chemical composition and the fuelwood value index (FVI) showed that by failing to efficiently utilise residues from Afzelia quanzensis, Millettia stuhlmannii and Pterocarpus angolensis, an opportunity to reduce some of the energy related problems is missed. An evaluation of effect of a mild wet torrefaction pretreatment showed that the chemical composition of the biochar is substantially different than the feedstock. The use of diluted acid as catalysts improves the biochar quality, namely in terms of the energy density and ash characteristics; however, the increment of the S content in the final product should be considered for market acceptance (because the fuels have a maximum allowance for S concentration). The thermal behaviour of the untreated and treated biomass was also investigated. The pyrolytic products of umbila and spruce were affected by the treatment and catalyst in terms of yield and composition of the vapours. / <p>QC 20150202</p>