Coal gasification in CO2 atmosphere and its kinetics since 1948: A brief review

Numerous coal gasification studies have been found in the literature those employed various kinds of gasifying agents such as steam and carbon dioxide. These studies are featured with wide variations in the parametric conditions and the usage of equipments. Steam is frequently employed as a gasifying agent, however, in several studies carbon dioxide has also been used as a gasifying agent either pure or in combination with other gasifying agents (H₂O, O₂, CO, H₂). This paper is a brief review of the coal gasification with CO₂ as a diluent. Different factors were studied over the coal gasification with CO₂ such as coal rank, pressure, temperature, gas composition, catalyst and the minerals present inside the coal, heating rate, particle size, and diverse reactor types. It also deals with the application of the gas-solid models developed in the literature and the combustion and gasification mechanisms for O₂/CO₂ streams. Moreover, it reviews the kinetics and the reaction rate equations (Arrhenius and Langmuir-Hinshelwood types) for coal-char gasification both in the reaction kinetic control region (low temperature) and the diffusion control region (high temperature) and at both low and high pressures.     

Detailed kinetic analysis and modelling of the dry gasification reaction of olive kernel and lignite coal chars

The dry gasification process of solid fuels is a promising pathway to mitigate and utilize captured CO₂ emissions toward syngas generation with tailored composition for several downstream energy conversion and chemical production processes. In the present work, comprehensive kinetic analysis and reaction modelling studies were carried out for olive kernel and lignite coal chars gasification reaction using pure CO₂ as gasifying agent. Chars reactivity and kinetics of the gasification reactions were thoroughly examined by thermogravimetric analysis at three different heating rates and correlated with their physicochemical properties. The reactivity of olive kernel char, as determined by the mean gasification reactivity and the comprehensive gasification characteristic index, S, was almost three times higher compared to that of the lignite coal char. It was disclosed that the fixed carbon content and alkali index (AI) have a major impact on the reactivity of chars. The activation energy, E_a, estimated by three different model-free kinetic methods was ranged between 140 and 170 kJ/mol and 250–350 kJ/mol for the olive kernel and lignite coal chars, respectively. The activation energy values for the lignite coal char significantly varied with carbon conversion degree, whereas this was not the case for olive kernel char, where the activation energy remained essentially unmodified throughout the whole carbon conversion range. Finally, the combined Malek and Coats-Rendfrem method was applied to unravel the mechanism of chars-CO₂ gasification reaction. It was found that the olive kernel char-CO₂ gasification can be described with a 2D-diffusion mechanism function (D2) whereas the lignite coal char-CO₂ gasification follows a second order chemical reaction mechanism function (F2).     

Options for net zero emissions hydrogen from Victorian lignite. Part 1: Gaseous and liquefied hydrogen

This two-part paper investigates the feasibility of producing export quantities (770 t/d) of blue hydrogen meeting international standards, by gasification of Victorian lignite plus carbon capture and storage (CCS). The study involves a detailed Aspen Plus simulation analysis of the entire production process, taking into account fugitive methane emissions during lignite mining. Part 1 focusses on the resources, energy requirements and greenhouse gas emissions associated with production of gaseous and liquefied hydrogen, while Part 2 focusses on production of ammonia as a hydrogen carrier.In this study, the proposed process comprises lignite mining, lignite drying and milling, air separation unit (ASU), dry-feed entrained flow gasification, gas cooling and cleaning, sour water-gas shift reaction, acid gas removal, pressure swing adsorption (PSA) for hydrogen purification, elemental sulphur recovery, CO₂ compression for transport and injection, hydrogen liquefaction, steam and gas turbines to generate all process power, plus an optional post-combustion CO₂ capture step. High grade waste heat is utilised for process heat and power generation. Three alternative process scenarios are investigated as options to reduce resource utilisation and greenhouse gas emissions: replacing the gas turbine with renewable energy from off-site wind turbines, and co-gasification of lignite with either biomass or biochar. In each case, the specific net greenhouse gas intensity is estimated and compared to the EU Taxonomy specification for sustainable hydrogen.This is the first time that a coal-to-hydrogen study has quantified the greenhouse gas emissions across the entire production chain, including upstream fugitive methane emissions. It is found that both gaseous and liquefied hydrogen can be produced from Victorian lignite, along with all necessary electricity, with specific emissions intensity (SEI) of 2.70 kg CO₂-e/kg H₂ and 2.73 kg CO₂-e/kg H₂, respectively. These values conform to the EU Taxonomy limit of 3.0 kg CO₂-e/kg H₂. This result is achieved using a Selexol™ plant for CO₂ capture, operating at 89.5%–91.7% overall capture efficiency. Importantly, the very low fugitive methane emissions associated with Victorian lignite mining is crucial to the low SEI of the process, making this is a critical advantage over the alternative natural gas or black coal processes.This study shows that there are technical options available to further reduce the SEI to meet tightening emissions targets. An additional post-combustion MDEA CO₂ capture unit can be added to increase the capture efficiency to 99.0%–99.2% and reduce the SEI to 0.3 kg CO₂-e/kg H₂. Emissions intensity can be further reduced by utilising renewable energy rather than co-production of electricity on site. Net zero emissions can then be achieved by co-gasification with ≤1.4 dry wt.% biomass, while a higher proportion of biomass would achieve net-negative emissions. Thus, options exist for production of blue hydrogen from Victorian lignite consistent with a ‘net zero by 2050’ target.     

A cryogen‐based peak‐shaving technology: systematic approach and techno‐economic analysis

A peak‐shaving technology is recently proposed, which integrates peak‐electricity generation, cryogenic energy storage and CO₂ capture. In such a technology, off‐peak electricity is used to produce liquid nitrogen and oxygen in an air separation and liquefaction unit. At peak hours, natural gas (or alternative gases, e.g. from gasification of coal) is burned by oxygen from the air separation unit (oxy‐fuel combustion) to generate electricity. CO₂ produced is captured in the form of dry ice. Liquid nitrogen produced in the air separation plant not only serves as an energy storage medium but also supplies the low‐grade cold energy for CO₂ separation. In addition, waste heat from the tail gas can be used to superheat nitrogen in the expansion process to further increase the system efficiency. This article reports a systematic approach, with an aim to provide technical information for the system design. Three potential blending gases (helium, oxygen and CO₂) are considered not only for assessing thermodynamic performance but also for techno‐economic analysis. The peak‐shaving systems are also compared with natural gas combined cycle and an oxy–natural gas combined cycle in terms of capital cost and peak electricity production cost. Copyright © 2011 John Wiley & Sons, Ltd.     

Process optimization and robustness analysis of municipal solid waste gasification using air‐carbon dioxide mixtures as gasifying agent

In this work, a computational fluid dynamics (CFD) model was coupled with an advanced statistical strategy combining design of experiments (DoE) and the Monte Carlo method to comparatively optimize and test the robustness of two municipal solid waste (MSW) gasification processes one using air‐carbon dioxide (CO₂) mixtures as a gasifying agent and the other using air alone. A 3^k full factorial design of 18 computer simulations was performed using as input factors for air‐CO₂ mixtures the equivalence ratio and CO₂‐to‐MSW ratio, while MSW feeding rate and air flow rate were used for air gasification. The selected responses were CO₂, H₂, CO, and C_nH_m generation, CH₄/H₂ and H₂/CO ratios, carbon conversion, and cold gas efficiency (CGE). Findings were that DoE allowed determining the best‐operating conditions to achieve optimal syngas quality. Monte Carlo identified the best‐operating conditions reaching a more stable high‐quality syngas. Air‐CO₂ mixture gasification showed enhanced responses with major improvements in CO₂ conversion and CGE, both up to a 13% increase. The optimal operating conditions that set the optimized responses showed to not always imply the most stable set of values to operate the system. Finally, this combined optimization process performance revealed to grant professionals the ability to make smarter decisions in an industrial environment.     

The effect of air staged combustion on NOx emissions in dried lignite combustion

Experiments were carried out in a multi-path air inlet one-dimensional furnace to assess NOx emission characteristics of the staged combustion of BRXL lignite and its dried coals. The impact of moisture content, multiple air staging, pulverized coal fineness and burnout air position on NOx emissions under deep, middle and shallow air-staged combustion conditions. Moreover, the impact of blending coals on NOx emissions was investigated in this paper. The unburned carbon concentration in fly ash was also tested. Experimental results based on the combustion of BRXL lignite and its dried coals show that NOx emissions can be reduced drastically by air-staged combustion. NOx emissions reduce with the increase of the air that is staged and the distance between the burner and burnout air position. Dried coal of BRXL lignite emits a smaller amount of NOx than that of BRXL lignite. However, the dried degree of BRXL lignite is closely related to R₉₀ fineness. Dried coal with optimal moisture content yields least NOx emissions. When deep or middle staged combustion was adopted, the application of multi-staged combustion is conducive to NOx reduction. However, when shallow staged combustion was adopted, NOx emissions are higher in multi-staged combustion than that in single-staged combustion with M_S = 0.54. Thus, the existence of a certain concentration of O₂ in reduction zone would significantly reduce NOx emissions. The blending coals that dried coals of BRXL lignite were blended with bituminous coals emit a larger amount of NOx than that of the dried coal alone. NOx emissions decrease with the increase of the proportion of dried coal in the blending coal. Moreover, the unburned carbon concentration in fly ash of dried coal in staged combustion is lower than that of BRXL lignite in staged combustion. On the whole, the dried coal of BRXL lignite is conducive to NOx reduction in staged combustion.     

Kinetics of woodchips char gasification with steam and carbon dioxide

Kinetics of woodchips char gasification has been examined. Steam and CO₂ were used as the gasifying agents. Differences and similarities between kinetics of steam gasification and CO₂ gasification have been discussed. Comparison was conducted in terms of gasification duration, evolution of reaction rate with time and/or conversion, and effect of partial pressure on reaction rate. Reactor temperature was maintained at 900 °C. Partial pressure of gasifying agents varied from 1.5 bars to 0.6 bars in intervals of 0.3 bars. Steam and CO₂ flow rates were chosen so that both gasifying agents had equal amount of oxygen content. CO₂ gasification lasted for about 60 min while steam gasification lasted for about 22 min. The average reaction rate for steam gasification was almost twice that of CO₂. Both reaction rate curves showed a peak value at certain degree of conversion. For steam gasification, the reaction rate peak was found to be at a degree of conversion of about 0.3. However, for CO₂ gasification the reaction rate peak was found to be at a conversion degree of about 0.1. Reaction rates have been fitted using the random pore model (RPM). Average structural parameter, ψ for steam gasification and CO₂ gasification was determined to be 9 and 2.1, respectively. Average rate constant at 900 °C was 0.065 min⁻¹ for steam gasification and 0.031 min⁻¹ for CO₂ gasification. Change in partial pressure of gasifying agents did not affect the reaction rate for both steam and CO₂ gasification.     

Integrated drying and gasification of wet microalgae biomass to produce H2 rich syngas – A thermodynamic approach by considering in-situ energy supply

A novel integrated drying and gasification of microalgae wet biomass process, involving a chemical-looping combustion (CLC) option to supply energy, is developed using Aspen Plus. The integrated gasification system consists of four primary units, including (i) a wet biomass drying unit, (ii) the gasification system, (iii) the CLC section, and (iv) the gas purification process. The model shows a good accuracy (relative error < 10%) in predicting the product compositions as compared to the experimental results under consistent operating conditions. The performance of the integrated gasification system is evaluated using Spirulina microalgae at various moisture contents (0–45 wt%). The effect of gasifying agents O₂/steam and the fraction of the produced char used in the CLC section on the gasification performance is also evaluated. The tar is successfully reformed into syngas in the pyrolysis stage by adjusting the O₂ flow rate. The C (char) to CLC provides to a positive effect on the syngas composition, particularly for gasification of wet biomass, but brings an adverse impact on the yield of the syngas product. The integration of the CLC process and CO₂ absorber in the gasification system provides high-quality syngas by removing CO₂. The separated pure CO₂ can be used as a feedstock for other chemical industries.     

Thermodynamic analysis of high‐ash coal‐fired power plant with carbon dioxide capture

A thermodynamic analysis of a 500‐MWe subcritical power plant using high‐ash Indian coal (base plant) is carried out to determine the effects of carbon dioxide (CO₂) capture on plant energy and exergy efficiencies. An imported (South African) low‐ash coal is also considered to compare the performance of the integrated plant (base plant with CO₂ capture plant). Chemical absorption technique using monoethanolamine as an absorbent is adopted in the CO₂ capture plant. The flow sheet computer program “Aspen Plus” is used for the parametric study of the CO₂ capture plant to determine the minimum energy requirement for absorbent regeneration at optimum absorber–stripper configuration. Energy and exergy analysis for the integrated plant is carried out using the power plant simulation software “Cycle‐Tempo”. The study also involves determining the effects of various steam extraction techniques from the turbine cycle (intermediate‐pressure–low‐pressure crossover pipe) for monoethanolamine regeneration. It is found that the minimum reboiler heat duty is 373 MW_th (equivalent to 3.77 MJ of heat energy per kg of CO₂ captured), resulting in a drop of plant energy efficiency by approximately 8.3% to 11.2% points. The study reveals that the maximum energy and exergy losses occur in the reboiler and the combustor, respectively, accounting for 29% and 33% of the fuel energy and exergy. Among the various options for preprocessing steam that is extracted from turbine cycle for reboiler use, “addition of new auxiliary turbine” is found to be the best option. Copyright © 2011 John Wiley & Sons, Ltd.     

Pre-combustion, post-combustion and oxy-combustion in thermal power plant for CO2 capture

This paper presents a summary of technical-economic studies. It allows evaluating, in the French context, the production cost of electricity derived from coal and gas power plants with the capture of CO₂, and the cost per tonne of CO₂ avoided. Three systems were studied: an Integrated Gasification Combined Cycle (IGCC), a conventional combustion of Pulverized Coal (PC) and a Natural Gas Combined Cycle (NGCC). Three main methods were envisaged for the capture of CO₂: pre-combustion, post-combustion and oxy-combustion.For the IGCC, two gasification types have been studied: a current technology based on gasification of dry coal at 27 bars (Shell or GE/Texaco radiant type) integrated into a classical combined cycle providing 320 MWe, and a future technology (planned for about 2015–2020) based on gasification of a coal–water mixture (slurry) that can be compressed to 64 bars (GE/Texaco slurry type) integrated into an advanced combined cycle (type H with steam cooling of the combustion turbine blades) producing a gross power output of 1200 MWe.     

Movable injection point–based syngas production in the context of underground coal gasification

Underground coal gasification (UCG) has been proven as a viable technology for the generation of high calorific value syngas using deep mine coal seams. The use of multiple injection points/movable injection point method could be an alternate technique for efficient gasification of high ash Indian coals. In this context, the present study is focused on evaluating the heating value of syngas using a variety of gasifying agents such as pure O₂, air, humidified O₂, and CO₂-O₂ dual-stage gasification under movable injection method for high ash coals. It is found that the use of movable injection point method had significantly increased the heating value of the product gas, compared with the fixed point injection method. For high and low ash coal under pure O₂ gasification, the calorific value of syngas obtained using movable injection point is 123.2 and 153.9 kJ/mol, which are 33.5% and 24.3% higher than the syngas calorific value obtained using fixed injection point, respectively. Further, the air as a gasification agent for high ash coals had increased the gross calorific value of the syngas by 24%, using this technology. The results of high ash coal gasification using humidified oxygen at optimum conditions (0.027-kg moisture/kg dry O₂) and CO₂-O₂ gas had enhanced the syngas calorific value by 12.6% and 5%, respectively. Humidified O₂ and CO₂-O₂ gasifying agents produced a high-quality syngas with the calorific value of 190 kJ/mol, among the gasifying agents used. The experimental results had shown that the movable injection point method is found to be a better alternative for the generation of calorific value-enriched syngas using high ash-based Indian coals.     

Effects of coal characteristics to performance of a highly efficient thermal power generation system based on pressurized oxy‐fuel combustion

Because of its fuel flexibility and high efficiency, pressurized oxy‐fuel combustion has recently emerged as a promising approach for efficient carbon capture and storage. One of the important options to design the pressurized oxy‐combustion is to determine method of coal (or other solid fuels) feeding: dry feeding or wet (coal slurry) feeding as well as grade of coals. The main aim of this research is to investigate effects of coal characteristics including wet or dry feeding on the performance of thermal power plant based on the pressurized oxy‐combustion with CO₂ capture versus atmospheric oxy‐combustion. A commercial process simulation tool (gCCS: the general carbon capture and storage) was used to simulate and analyze an advanced ultra‐supercritical(A‐USC) coal power plant under pressurized and atmospheric oxy‐fuel conditions. The design concept is based on using pure oxygen as an oxidant in a pressurized system to maximize the heat recovery through process integration and to reduce the efficiency penalty because of compression and purification units. The results indicate that the pressurized case efficiency at 30 bars was greater than the atmospheric oxy‐fuel combustion (base line case) by 6.02% when using lignite coal firing. Similarly, efficiency improvements in the case of subbituminous and bituminous coals were around 3% and 2.61%, respectively. The purity of CO₂ increased from 53.4% to 94% after compression and purification. In addition, the study observed the effects of coal‐water slurry using bituminous coal under atmospheric conditions, determining that the net plant efficiency decreased by 3.7% when the water content in the slurry increased from 11.12% to 54%. Copyright © 2016 John Wiley & Sons, Ltd.     

Effect of supplementary firing options on cycle performance and CO2 emissions of an IGCC power generation system

Supplementary firing is adopted in combined‐cycle power plants to reheat low‐temperature gas turbine exhaust before entering into the heat recovery steam generator. In an effort to identify suitable supplementary firing options in an integrated gasification combined‐cycle (IGCC) power plant configuration, so as to use coal effectively, the performance is compared for three different supplementary firing options. The comparison identifies the better of the supplementary firing options based on higher efficiency and work output per unit mass of coal and lower CO₂ emissions. The three supplementary firing options with the corresponding fuel used for the supplementary firing are: (i) partial gasification with char, (ii) full gasification with coal and (iii) full gasification with syngas. The performance of the IGCC system with these three options is compared with an option of the IGCC system without supplementary firing. Each supplementary firing option also involves pre‐heating of the air entering the gas turbine combustion chamber in the gas cycle and reheating of the low‐pressure steam in the steam cycle. The effects on coal consumption and CO₂ emissions are analysed by varying the operating conditions such as pressure ratio, gas turbine inlet temperature, air pre‐heat and supplementary firing temperature. The results indicate that more work output is produced per unit mass of coal when there is no supplementary firing. Among the supplementary firing options, the full gasification with syngas option produces the highest work output per unit mass of coal, and the partial gasification with char option emits the lowest amount of CO₂ per unit mass of coal. Based on the analysis, the most advantageous option for low specific coal consumption and CO₂ emissions is the supplementary firing case having full gasification with syngas as the fuel. Copyright © 2008 John Wiley & Sons, Ltd.     

Steam gasification of Greek lignite and its chars by co-feeding CO2 toward syngas production with an adjustable H2/CO ratio

Low-rank lignite is among the most abundant and cheap fossil fuels, linked, however, to serious environmental implications when employed as feedstock in conventional thermoelectric power plants. Hence, toward a low-carbon energy transition, the role of coal in world's energy mix should be reconsidered. In this regard, coal gasification for synthesis gas generation and consequently through its upgrade to a variety of value-added chemicals and fuels constitutes a promising alternative. Herein, we thoroughly explored for a first time the steam gasification reactivity of Greek Lignite (LG) and its derived chars obtained by raw LG thermal treatment at 300, 500 and 800 °C. Moreover, the impact of CO₂ addition on H₂O gasifying agent mixtures was also investigated. Both the pristine and char samples were fully characterized by various physicochemical techniques to gain insight into possible structure-gasification relationships. The highest syngas yield was obtained for chars derived after LG thermal treatment at 800 °C, due mainly to their high content in fixed carbon, improved textural properties and high alkali index. Steam gasification of lignite and char samples led to H₂-rich syngas mixtures with a H₂/CO ratio of approximately 3.8. However, upon co-feeding CO₂ and H₂O, the H₂/CO ratio can be suitably adjusted for several potential downstream processes.     

Impact of choice of CO2 separation technology on thermo‐economic performance of Bio‐SNG production processes

Three different CO₂ separation technologies for production of synthetic natural gas (SNG) from biomass gasification – amine‐based absorption, membrane‐based separation and pressure swing adsorption – are investigated for their thermo‐economic performance against the background of different possible future energy market scenarios. The studied scale of the SNG plant is a thermal input of 100 MW_th,LHV to the gasifier at a moisture content of 20 wt‐% with a preceding drying step reducing the biomass' natural moisture content of 50 wt‐%. Preparation of the CO₂‐rich stream for carbon capture and storage is investigated for the amine‐based absorption and the membrane‐based separation technology alternatives. The resulting cold gas efficiency η_cg for the investigated process alternatives ranges between 0.65 and 0.695. The overall system efficiency η_sys ranges from 0.744 to 0.793, depending on both the separation technology and the background energy system. Amine‐based absorption gives the highest cold gas efficiency whereas the potential for cogeneration of electricity from the process' excess heat is higher for membrane‐based separation and pressure swing adsorption. The estimated specific production costs for SNG c_SNG for a process input of 90.3 MW_th,LHV at 50 wt‐% moisture vary between 103–127 €₂₀₁₀/MWh_SNG. The corresponding production subsidy level c_subsidy needed to achieve end‐user purchase price‐parity with fossil natural gas is in the range of 56–78 €₂₀₁₀/MWh_SNG depending on both the energy market scenario and the CO₂ separation technology. Sensitivity analysis on the influence of changes in the total capital cost for the SNG plant on the production cost indicates a decrease of about 12% assuming a 30% reduction in total capital investment. Capture and storage of biogenic CO₂ – if included in the emission trading system – only becomes an option at higher CO₂ charges. This is due to increased investment costs but, in particular, due to the rather high costs for CO₂ transport and storage that have been assumed in this study. Copyright © 2013 John Wiley & Sons, Ltd.     

Evaluation of Mg‐MOF‐74 for post‐combustion carbon dioxide capture through pressure swing adsorption

This paper presents a computational study of an energy‐efficient technique for post‐combustion CO₂ capture using novel material, namely, Mg‐MOF‐74, using pressure swing adsorption (PSA) processes. A detailed one‐dimensional, transient mathematical model has been formulated to include the heat and mass transfer, the pressure drop and multicomponent mass diffusion. The PSA model has been further extended by incorporating a heat regenerating process to enhance CO₂ sequestration. The heat dissipated during adsorption is stored in packed sand bed and released during desorption step for heating purpose. The model has been implemented on a MATLAB program using second‐order discretization. Validation of the model was performed using a complete experimental data set for CO₂ sequestration using zeolite 13X. Simulation of the PSA experiment on fixed bed has been carried out to evaluate the capacity of Mg‐MOF‐74 for CO₂ capture with varying feed gas temperature of 28 and 100 °C, varying pressurization and purge times and heat regeneration. It was discovered that the PSA process with heat regeneration system might be advantageous because it achieves equivalent amount of CO₂ sequestration in fewer PSA cycles compared with PSA without heat regeneration system. Based on the simulated conditions, CO₂ recovery with Mg‐MOF‐74 gives high percentage purity (above 98%) for the captured CO₂. Copyright © 2015 John Wiley & Sons, Ltd.     

A review of recent developments in carbon capture utilizing oxy‐fuel combustion in conventional and ion transport membrane systems

Fossil fuels provide a significant fraction of the global energy resources, and this is likely to remain so for several decades. Carbon dioxide (CO₂) emissions have been correlated with climate change, and carbon capture is essential to enable the continuing use of fossil fuels while reducing the emissions of CO₂ into the atmosphere thereby mitigating global climate changes. Among the proposed methods of CO₂ capture, oxyfuel combustion technology provides a promising option, which is applicable to power generation systems. This technology is based on combustion with pure oxygen (O₂) instead of air, resulting in flue gas that consists mainly of CO₂ and water (H₂O), that latter can be separated easily via condensation, while removing other contaminants leaving pure CO₂ for storage. However, fuel combustion in pure O₂ results in intolerably high combustion temperatures. In order to provide the dilution effect of the absent nitrogen (N₂) and to moderate the furnace/combustor temperatures, part of the flue gas is recycled back into the combustion chamber. An efficient source of O₂ is required to make oxy‐combustion a competitive CO₂ capture technology. Conventional O₂ production utilizing the cryogenic distillation process is energetically expensive. Ceramic membranes made from mixed ion‐electronic conducting oxides have received increasing attention because of their potential to mitigate the cost of O₂ production, thus helping to promote these clean energy technologies. Some effort has also been expended in using these membranes to improve the performance of the O₂ separation processes by combining air separation and high‐temperature oxidation into a single chamber. This paper provides a review of the performance of combustors utilizing oxy‐fuel combustion process, materials utilized in ion‐transport membranes and the integration of such reactors in power cycles. The review is focused on carbon capture potential, developments of oxyfuel applications and O₂ separation and combustion in membrane reactors. The recent developments in oxyfuel power cycles are discussed focusing on the main concepts of manipulating exergy flows within each cycle and the reported thermal efficiencies. Copyright © 2010 John Wiley & Sons, Ltd.     

Study on different zero CO2 emission IGCC systems with CO2 capture by integrating OTM

In this paper, different zero CO₂ emission integrated gasification combined cycle (IGCC) systems based on the oxy‐fuel combustion method by integrating with oxygen ion transfer membrane (OTM) with and without sweep gas are proposed in order to reduce the energy consumption of CO₂ capture. By utilizing the Aspen Plus software, the overall system models are established. The performances of the proposed systems are compared with the traditional IGCC system without CO₂ capture and the zero CO₂ emission IGCC system based on the oxy‐fuel combustion method using the cryogenic air separation unit. In addition, the effects of OTM key parameters on the proposed system performance, such as the feed side pressure, permeate side pressure, and operating temperature, are investigated and analyzed. The results show that the efficiency of the zero CO₂ emission IGCC system based on the oxy‐fuel combustion method integrated with OTM without sweep gas is 6.67% lower than that of the traditional IGCC system without CO₂ capture, but 1.88% higher than that of the zero CO₂ emission IGCC system using the cryogenic air separation unit, and 0.64% lower than that of the proposed system with sweep gas. The research achievements will provide valuable references for further study on CO₂ capture based on IGCC with lower energy penalty. Copyright © 2016 John Wiley & Sons, Ltd.     

Implications of system expansion for the assessment of well‐to‐wheel CO2 emissions from biomass‐based transportation

In this paper we show the effects of expanding the system when evaluating well‐to‐wheel (WTW) CO₂ emissions for biomass‐based transportation, to include the systems surrounding the biomass conversion system. Four different cases are considered: DME via black liquor gasification (BLG), methanol via gasification of solid biomass, lignocellulosic ethanol and electricity from a biomass integrated gasification combined cycle (BIGCC) used in a battery‐powered electric vehicle (BPEV). All four cases are considered with as well as without carbon capture and storage (CCS). System expansion is used consistently for all flows. The results are compared with results from a conventional WTW study that only uses system expansion for certain co‐product flows. It is shown that when expanding the system, biomass‐based transportation does not necessarily contribute to decreased CO₂ emissions and the results from this study in general indicate considerably lower CO₂ mitigation potential than do the results from the conventional study used for comparison. It is shown that of particular importance are assumptions regarding future biomass use, as by expanding the system, future competition for biomass feedstock can be taken into account by assuming an alternative biomass usage. Assumptions regarding other surrounding systems, such as the transportation and the electricity systems are also shown to be of significance. Of the four studied cases without CCS, BIGCC with the electricity used in a BPEV is the only case that consistently shows a potential for CO₂ reduction when alternative use of biomass is considered. Inclusion of CCS is not a guarantee for achieving CO₂ reduction, and in general the system effects are equivalent or larger than the effects of CCS. DME from BLG generally shows the highest CO₂ emission reduction potential for the biofuel cases. However, neither of these options for biomass‐based transportation can alone meet the needs of the transport sector. Therefore, a broader palette of solutions, including different production routes, different fuels and possibly also CCS, will be needed. Copyright © 2009 John Wiley & Sons, Ltd.     

A comprehensive techno‐economic analysis method for power generation systems with CO2 capture

A new comprehensive techno‐economic analysis method for power generation systems with CO₂ capture is proposed in this paper. The correlative relationship between the efficiency penalty, investment increment, and CO₂ avoidance cost is established. Through theoretical derivation, typical system analysis, and variation trends investigation, the mutual influence between technical and economic factors and their impacts on the CO₂ avoidance cost are studied. At the same time, the important role that system integration plays in CO₂ avoidance is investigated based on the analysis of a novel partial gasification CO₂ recovery system. The results reveal that for the power generation systems with CO₂ capture, the efficiency penalty not only affects the costs on fuel, but the incremental investment cost for CO₂ capture (U.S.$ kW⁻¹) as well. Consequently, it will have a decisive impact on the CO₂ avoidance cost. Therefore, the added attention should be paid to improve the technical performance in order to reduce the efficiency penalty in energy system with CO₂ capture and storage. Additionally, the system integration may not only decrease the efficiency penalty, but also simplify the system structure and keep the investment increment at a low level, and thereby it reduces the CO₂ avoidance cost significantly. For example, for the novel partial gasification CO₂ recovery system, owing to system integration, its efficiency can reach 42.2%, with 70% of CO₂ capture, and its investment cost is only 87$ kW⁻¹ higher than that of the reference IGCC system, thereby the CO₂ avoidance cost is only 6.23$ t⁻¹ CO₂. The obtained results provide a comprehensive technical–economical analysis method for energy systems with CO₂ capture useful for reducing the avoidance costs. Copyright © 2009 John Wiley & Sons, Ltd.