Techno-economic evaluation of advanced IGCC lignite coal fuelled power plants with CO2 capture

The techno-economic evaluation of four novel integrated gasification combined cycle (IGCC) power plants fuelled with low rank lignite coal with CO₂ capture facility has been investigated using ECLIPSE process simulator. The performance of the proposed plants was compared with two conventional IGCC plants with and without CO₂ capture. The proposed plants include an advanced CO₂ capturing process based on the Absorption Enhanced Reforming (AER) reaction and the regeneration of sorbent materials avoiding the need for sulphur removal component, shift reactor and/or a high temperature gas cleaning process. The results show that the proposed CO₂ capture plants efficiencies were 18.5–21% higher than the conventional IGCC CO₂ capture plant. For the proposed plants, the CO₂ capture efficiencies were found to be within 95.8–97%. The CO₂ capture efficiency for the conventional IGCC plant was 87.7%. The specific investment costs for the proposed plants were between 1207 and 1479 €/kW_e and 1620 €/kW_e and 1134 €/kW_e for the conventional plants with and without CO₂ capture respectively. Overall the proposed IGCC plants are cleaner, more efficient and produce electricity at cheaper price than the conventional IGCC process.     

Economical assessment of competitive enhanced limestones for CO2 capture cycles in power plants

CO₂ capture systems based on the carbonation/calcination loop have gained rapid interest due to promising carbonator CO₂ capture efficiency, low sorbent cost and no flue gases treatment is required before entering the system. These features together result in a competitively low cost CO₂ capture system. Among the key variables that influence the performance of these systems and their integration with power plants, the carbonation conversion of the sorbent and the heat requirement at calciner are the most relevant. Both variables are mainly influenced by CaO/CO₂ ratio and make-up flow of solids. New sorbents are under development to reduce the decay of their carbonation conversion with cycles. The aim of this study is to assess the competitiveness of new limestones with enhanced sorption behaviour applied to carbonation/calcination cycle integrated with a power plant, compared to raw limestone. The existence of an upper limit for the maximum average capture capacity of CaO has been considered. Above this limit, improving sorbent capture capacity does not lead to the corresponding increase in capture efficiency and, thus, reduction of CO₂ avoided cost is not observed. Simulations calculate the maximum price for enhanced sorbents to achieve a reduction in CO₂ removal cost under different process conditions (solid circulation and make-up flow). The present study may be used as an assessment tool of new sorbents to understand what prices would be competitive compare with raw limestone in the CO₂ looping capture systems.     

Enhancement of Ca‐Based Sorbent Multicyclic Behavior in Ca Looping Process for CO2 Separation

The Ca‐based sorbent looping cycle represents an innovative way of CO₂ capture for power plants. However, the CO₂ capture capacity of the Ca‐based sorbent decays sharply with calcination/carbonation cycle number increasing. In order to improve the CO₂ capture capacity of the sorbent in the Ca looping cycle, limestone was modified with acetic acid solution. The cyclic carbonation behaviors of the modified and original limestones were investigated in a twin fixed‐bed reactor system. The modified limestone possesses better cyclic carbonation kinetics than the original limestone at each cycle. The modified limestone carbonated at 640–660 °C achieves the optimum carbonation conversion. The acetic acid modification improves the long‐term performance of limestone, resulting in directly measured conversion as high as 0.4 after 100 cycles, while the original limestone remains at a conversion of less than 0.1 at the same reaction conditions. Both the pore volume and pore area distributions of the calcines derived from the modified limestone are better than those derived from the original limestone. The CO₂ partial pressure for carbonation has greater effect on conversion of the original limestone than on that of the modified sorbent because of the difference in their pore structure characteristics. The carbonation conversion of the original limestone decreases with the increase in particle size, while the change in particle size of the modified sorbent has no clear effect on cyclic carbonation behavior.     

Integration of a Ca looping system for CO2 capture in existing power plants

This work analyses a Ca looping system that uses CaO as regenerable sorbent to capture CO₂ from the flue gases generated in power plants. The CO₂ is captured by CaO in a CFB carbonator while coal oxycombustion provides the energy required to regenerate the sorbent. Part of the energy introduced into the calciner can be transferred to a new supercritical steam cycle to generate additional power. Several case studies have been integrated with this steam cycle. Efficiency penalties, mainly associated with the energy consumption of the ASU, CO₂ compressor and auxiliaries, can be as low as 7.5% p. of net efficiency when working with low‐CaCO₃ make‐up flows and integrating the Ca looping with a cement plant that makes use of the spent sorbent. The penalties increase to 8.3% p. when this possibility is not available. Operation conditions aiming at minimum calciner size result in slightly higher‐efficiency penalties. © 2010 American Institute of Chemical Engineers AIChE J, 2011     

Techno-economic optimization of IGCC integrated with utility system for CO2 emissions reduction—Maximum power production in IGCC

Environmental legislation, with its increasing pressure on the energy sector to control greenhouse gases, is a driving force to reduce CO₂ emissions. In this paper, pre-combustion CO₂ capture through integration of a site utility system with an integrated gasification combined cycle (IGCC) is investigated as an option to provide a compressed CO₂-rich stream from a process site for sequestration. This work presents a two-step procedure for integration and optimization of a site utility system with an IGCC plant: (i) screening and optimization of IGCC plant performance parameters; (ii) integration and optimization of the utility system of the site with the IGCC plant. In the first step, an optimization approach applies the results of screening studies based on rigorous simulation of the IGCC. Having fixed the inlet fuel flow rate, the IGCC design parameters (including oxygen consumption, diluent flow rate and turbine exit pressure) are optimized for maximum power generation. Energy flows between the IGCC and CO₂ compression train are considered. In the second step, the economic and operating performance of the utility system integrated with the IGCC plant are modeled and optimized for minimum operating cost to find the most appropriate level of integration. In a case study illustrating the approach, 94% of the fuel is gasified; additional power generation offsets the operating costs of pre-combustion CO₂ capture.     

Cost of energy analysis of integrated gasification combined cycle (IGCC) power plant with respect to CO2 capture ratio under climate change scenarios

This paper presents the results of the cost of energy (COE) analysis of an integrated gasification combined cycle (IGCC) power plant with respect to CO₂ capture ratio under the climate change scenarios. To obtain process data for a COE analysis, simulation models of IGCC power plants and an IGCC with carbon capture and sequestration (CCS) power plant, developed by the United States Department of Energy (DOE) and National Energy Technology Laboratory (NETL), have been adopted and simulated using Aspen Plus. The concept of 20-year levelized cost of energy (LCOE), and the climate change scenarios suggested by International Energy Agency (IEA) are also adopted to compare the COE of IGCC power plants with respect to CO₂ capture ratio more realistically. Since previous studies did not consider fuel price and CO₂ price changes, the reliability of previous results of LCOE is not good enough to be accepted for an economic comparison of IGCC power plants with respect to CO₂ capture ratio. In this study, LCOEs which consider price changes of fuel and CO₂ with respect to the climate change scenarios are proposed in order to increase the reliability of an economic comparison. And the results of proposed LCOEs of an IGCC without CCS power plant and IGCC with CCS (30%, 50%, 70% and 90% capture-mole basis- of CO₂ in syngas stream) power plants are presented.     

烟气中水蒸气对钙基吸收剂碳酸化的影响特性

在循环煅烧/碳酸化反应系统上考察煅烧气氛和碳酸化气氛中水蒸气含量以及CO₂分压对钙基吸收剂成型颗粒碳酸化的影响,通过对钙基吸收剂微观结构分析(扫描电镜、氮吸附分析)以理解水蒸气影响碳酸化特性的机理。结果表明,煅烧气氛和碳酸化气氛中的水蒸气均可提高钙基吸收剂的碳酸化转化率,水蒸气含量分别为10%和5%时,吸收剂的碳酸化性能较好;水蒸气在碳酸化气氛中对高铝水泥改性吸收剂的改善作用较石灰石显著。煅烧气氛中的CO₂分压越高,烧结现象越严重,降低钙基吸收剂的捕集效率;碳酸化气氛CO₂分压提高,有利于提高钙基吸收剂的碳酸化转化率。烟气中水蒸气丰富了吸收剂的微观孔隙,使得吸收剂捕集CO₂性能得到改善。     

Modelling of an IGCC plant with carbon capture for 2020

Currently several industrial scale IGCC - carbon capture demonstration plants are being planned. Thermodynamic simulations are a useful tool to investigate the optimal plant configuration. In order to demonstrate the potential of the next generation of IGCC with CCS a thermodynamic model was developed using conventional but improved technology. The plant concept was verified and simulated for a generic hard coal and lignite. The simulation showed a net efficiency (LHV) of 38.5% and 41.9% for hard coal and lignite, respectively.The results are consistent with current studies but also indicate that major simulations were too optimistic. The auxiliary demand of an IGCC plant with carbon capture can be expected with 21 to 24% based on gross output. The drop in efficiency compared to the none-capture case is estimated with roughly 11 to 12%-points. During a sensitivity study the impact of process changes on plant efficiency and economics is evaluated. Releasing the captured CO₂ without compression is found to be economically favourable at CO₂ prices below 15 €/t and electricity prices above 100 €/MWh. Further the impact of carbon capture rate is quantified and an efficiency potential is indicated for lower CO₂ quality.     

Optimal design and integration of an air separation unit (ASU) for an integrated gasification combined cycle (IGCC) power plant with CO2 capture

The air separation unit (ASU) plays a key role in improving the efficiency, availability, and operability of an oxygen-fed integrated gasification combined cycle (IGCC) power plant. An optimal integration between the ASU and the balance of the plant, especially the gasifier and the gas turbine (GT), has significant potential for enhancing the overall plant efficiency. Considering the higher operating pressure of the GT, an elevated-pressure air separation unit (EP-ASU) is usually favored instead of the conventional low-pressure air separation units (LP-ASU). In addition, a pumped liquid oxygen (PLOX) cycle is usually chosen if the operating pressure of the gasifier is high. A PLOX cycle helps to improve plant safety and availability and to decrease the capital cost by reducing the size of the oxygen compressor or by eliminating it completely. However, the refrigeration lost in withdrawn liquid oxygen must be efficiently recovered. This paper considers five different configurations of an ASU with PLOX cycle and compares their power consumptions with an EP-ASU with a traditional gaseous oxygen (GOX) cycle. The study shows that an optimally designed EP-ASU with a PLOX cycle can have similar power consumption to that of an EP-ASU with GOX cycle in the case of 100% nitrogen integration. In the case of an IGCC with pre-combustion CO₂ capture, the lower heating value (LHV) of the shifted syngas, both on a mass and volumetric basis, is in between the LHV of the unshifted syngas from an IGCC plant and the LHV of natural gas, for which the GTs are generally designed. The optimal air integration in the case of a shifted syngas is found to be much lower than that of an unshifted syngas. This paper concurs with the existing literature that the optimal integration occurs when air extracted from the GT can be replaced with the nitrogen from the ASU without exceeding mass/volumetric flow limitations of the GT. Considering nitrogen and air integration between the ASU and the GT, this paper compares the power savings in an LP-ASU with a PLOX cycle to the power savings in an EP-ASU with GOX cycle and EP-ASU with PLOX cycle. The results show that an LP-ASU with a PLOX cycle has less power consumption if the nitrogen integration levels are less than 50-60%. In addition, a study is carried out by varying the concentration of nitrogen and steam in the fuel diluents to the GT while the NOx level was maintained constant. The study shows that when the nitrogen injection rate exceeds 50%, an EP-ASU with a PLOX cycle is a better option than an LP-ASU with a PLOX cycle. This paper shows that an optimal design and integration of an ASU with the balance of the plant can help to increase the net power generation from an IGCC plant with CO₂ capture.     

Optimization of energy usage for fleet‐wide power generating system under carbon mitigation options

This article presents a fleet‐wide model for energy planning that can be used to determine the optimal structure necessary to meet a given CO₂ reduction target while maintaining or enhancing power to the grid. The model incorporates power generation as well as CO₂ emissions from a fleet of generating stations (hydroelectric, fossil fuel, nuclear, and wind). The model is formulated as a mixed integer program and is used to optimize an existing fleet as well as recommend new additional generating stations, carbon capture and storage, and retrofit actions to meet a CO₂ reduction target and electricity demand at a minimum overall cost. The model was applied to the energy supply system operated by Ontario power generation (OPG) for the province of Ontario, Canada. In 2002, OPG operated 79 electricity generating stations; 5 are fueled with coal (with a total of 23 boilers), 1 by natural gas (4 boilers), 3 nuclear, 69 hydroelectric and 1 wind turbine generating a total of 115.8 TWh. No CO₂ capture process existed at any OPG power plant; about 36.7 million tonnes of CO₂ was emitted in 2002, mainly from fossil fuel power plants. Four electricity demand scenarios were considered over a span of 10 years and for each case the size of new power generation capacity with and without capture was obtained. Six supplemental electricity generating technologies have been allowed for: subcritical pulverized coal‐fired (PC), PC with carbon capture (PC+CCS), integrated gasification combined cycle (IGCC), IGCC with carbon capture (IGCC+CCS), natural gas combined cycle (NGCC), and NGCC with carbon capture (NGCC+CCS). The optimization results showed that fuel balancing alone can contribute to the reduction of CO₂ emissions by only 3% and a slight, 1.6%, reduction in the cost of electricity compared to a calculated base case. It was found that a 20% CO₂ reduction at current electricity demand could be achieved by implementing fuel balancing and switching 8 out of 23 coal‐fired boilers to natural gas. However, as demand increases, more coal‐fired boilers needed to be switched to natural gas as well as the building of new NGCC and NGCC+CCS for replacing the aging coal‐fired power plants. To achieve a 40% CO₂ reduction at 1.0% demand growth rate, four new plants (2 NGCC, 2 NGCC+CCS) as well as carbon capture processes needed to be built. If greater than 60% CO₂ reductions are required, NGCC, NGCC+CCS, and IGCC+CCS power plants needed to be put online in addition to carbon capture processes on coal‐fired power plants. The volatility of natural gas prices was found to have a significant impact on the optimal CO₂ mitigation strategy and on the cost of electricity generation. Increasing the natural gas prices resulted in early aggressive CO₂ mitigation strategies especially at higher growth rate demands. © 2009 American Institute of Chemical Engineers AIChE J, 2009     

The calcium looping cycle for CO2 capture from power generation, cement manufacture and hydrogen production

Calcium looping is a CO₂ capture scheme using solid CaO-based sorbents to remove CO₂ from flue gases, e.g., from a power plant, producing a concentrated stream of CO₂ (∼95%) suitable for storage. The scheme exploits the reversible gas-solid reaction between CO₂ and CaO(s) to form CaCO₃(s). Calcium looping has a number of advantages compared to closer-to-market capture schemes, including: the use of circulating fluidised bed reactors—a mature technology at large scale; sorbent derived from cheap, abundant and environmentally benign limestone and dolomite precursors; and the relatively small efficiency penalty that it imposes on the power/industrial process (i.e., estimated at 6-8 percentage points, compared to 9.5-12.5 from amine-based post-combustion capture). A further advantage is the synergy with cement manufacture, which potentially allows for decarbonisation of both cement manufacture and power production. In addition, a number of advanced applications offer the potential for significant cost reductions in the production of hydrogen from fossil fuels coupled with CO₂ capture. The range of applications of calcium looping are discussed here, including the progress made towards demonstrating this technology as a viable post-combustion capture technology using small-pilot scale rigs, and the early progress towards a 2 MW scale demonstrator.     

CO2 capture from flue gases using a fluidized bed reactor with limestone

The CO₂ capture from flue gases by a small fluidized bed reactor was experimentally investigated with limestone. The results showed that CO₂ in flue gases could be captured by limestone with high efficiency, but the CO₂ capture capacity of limestone decayed with the increasing of carbonation/calcination cycles. From a practical point of view, coal may be required to provide the heat for CaCO₃ calcination, resulting in some potential effect on the sorbent capacity of CO₂ capture. Experiment results indicated that the variation in the capacity of CO₂ capture by using a limestone/coal ash mixture with a cyclic number was qualitatively similar to the variation of the capacity of CO₂ capture using limestone only. Cyclic stability of limestone only undergoing the kinetically controlled stage in the carbonation process had negligible difference with that of the limestone undergoing both the kinetically controlled stage and the product layer diffusion controlled stage. Based on the experimental data, a model for the high-velocity fluidized bed carbonator that consists of a dense bed zone and a riser zone was developed. The model predicted that high CO₂ capture efficiencies (>80%) were achievable for a range of reasonable operating conditions by the high-velocity fluidized bed carbonator in a continuous carbonation and calcination system.     

Techno-economic assessment of pulverized coal boilers and IGCC power plants with CO<Subscript>2</Subscript> capture

The current studies on power plant technologies suggest that Integrated Gasification Combined Cycle (IGCC) systems are an effective and economic CO₂ capture technology pathway. In addition, the system in conventional configuration has the advantage of being more “CO₂ capture ready” than other technologies. Pulverized coal boilers (PC) have, however, proven high technical performance attributes and are economically often most practical technologies. To highlight the pros and cons of both technologies in connection with an integrated CO₂ capture, a comparative analysis of ultrasupercritical PC and IGCC is carried out in this paper. The technical design, the mass and energy balance and the system optimizations are implemented by using the ECLIPSE chemical plant simulation software package. Built upon these technologies, the CO₂ capture facilities are incorporated within the system. The most appropriate CO₂ capture systems for the PC system selected for this work are the oxy-fuel system and the postcombustion scheme using Monoethanolamine solvent scrubber column (MEA). The IGCC systems are designed in two configurations: Water gas shift reactor and Selexol-based separation. Both options generate CO₂-rich and hydrogen rich-gas streams. Following the comparative analysis of the technical performance attributes of the above cycles, the economic assessment is carried out using the economic toolbox of ECLIPSE is seamlessly connected to the results of the mass and energy balance as well as the utility usages. The total cost assessment is implemented according to the step-count exponential costing method using the dominant factors and/or a combination of parameters. Subsequently, based on a set of assumptions, the net present value estimation is implemented to calculate the breakeven electricity selling prices and the CO₂ avoidance cost.     

Techno-economic assessment of pulverized coal boilers and IGCC power plants with CO2 capture

The current studies on power plant technologies suggest that Integrated Gasification Combined Cycle (IGCC) systems are an effective and economic CO₂ capture technology pathway. In addition, the system in conventional configuration has the advantage of being more “CO₂ capture ready” than other technologies. Pulverized coal boilers (PC) have, however, proven high technical performance attributes and are economically often most practical technologies. To highlight the pros and cons of both technologies in connection with an integrated CO₂ capture, a comparative analysis of ultrasupercritical PC and IGCC is carried out in this paper. The technical design, the mass and energy balance and the system optimizations are implemented by using the ECLIPSE chemical plant simulation software package. Built upon these technologies, the CO₂ capture facilities are incorporated within the system. The most appropriate CO₂ capture systems for the PC system selected for this work are the oxy-fuel system and the postcombustion scheme using Monoethanolamine solvent scrubber column (MEA). The IGCC systems are designed in two configurations: Water gas shift reactor and Selexol-based separation. Both options generate CO₂-rich and hydrogen rich-gas streams. Following the comparative analysis of the technical performance attributes of the above cycles, the economic assessment is carried out using the economic toolbox of ECLIPSE is seamlessly connected to the results of the mass and energy balance as well as the utility usages. The total cost assessment is implemented according to the step-count exponential costing method using the dominant factors and/or a combination of parameters. Subsequently, based on a set of assumptions, the net present value estimation is implemented to calculate the breakeven electricity selling prices and the CO₂ avoidance cost.     

Increasing Porosity of Molded Calcium‐Based Sorbents by Glucose Templating for Cyclic CO2 Capture

With the aim to enhance the CO₂ capture capacity and anti‐attrition property of CaO‐based sorbents simultaneously, a novel CaO‐based sphere was prepared by extrusion‐spheronization using Ca(OH)₂ powder with glucose templating. The CO₂ capture characteristics and attrition resistance property of the sorbent were examined and the microstructure of the sorbents was analyzed. The results demonstrate that the obtained spherical sorbents exhibit an outstanding anti‐attrition performance compared to limestone sorbent. After 100 cycles, all of the templated sorbents hold a CO₂ capture capacity of more than one time higher than that of limestone. The optimum templating rate of glucose in the sorbent was 1–5 wt %.     

Influence of calcination conditions on carrying capacity of CaO-based sorbent in CO2 looping cycles

This study examines the loss of sorbent activity caused by sintering under realistic CO₂ capture cycle conditions. The samples tested here included two limestones: Havelock limestone from Canada (New Brunswick) and a Polish (Upper Silesia) limestone (Katowice). Samples were prepared both in a thermogravimetric analyzer (TGA) and a tube furnace (TF). Two calcination conditions were employed: in N₂ at lower temperature; and in CO₂ at high temperature. The samples obtained were observed with a scanning electron microscope (SEM) and surface compositions of the resulting materials were analyzed by the energy dispersive X-ray (EDX) method. The quantitative influence of calcination conditions was examined by nitrogen adsorption/desorption tests, gas displacement pycnometry and powder displacement pycnometry; BET surface areas, BJH pore volume distributions, skeletal densities and envelope densities were determined. The SEM images showed noticeably larger CaO sub-grains were produced by calcination in CO₂ during numerous cycles than those seen with calcination in nitrogen. The EDX elemental analyses showed a strong influence of impurities on local melting at the sorbent particle surface, which became more pronounced at higher temperature. Results of BET/BJH testing clearly support these findings on the effect of calcination/cycling conditions on sorbent morphology. Envelope density measurements showed that particles displayed densification upon cycling and that particles calcined under CO₂ showed greater densification than those calcined under N₂. Interestingly, the Katowice limestone calcined/cycled at higher temperature in CO₂ showed an increase of activity for cycles involving calcination under N₂ in the TGA. These results clearly demonstrate that, in future development of CaO-based CO₂ looping cycle technology, more attention should be paid to loss of sorbent activity caused by realistic calcination conditions and the presence of impurities originating from fuel ash and/or limestone.     

Lime enhanced gasification of solid fuels: Examination of a process for simultaneous hydrogen production and CO2 capture

The lime enhanced gasification (LEGS) process uses CaO as a CO₂ carrier and consists of two coupled reactors: a gasifier in which CO₂ absorption by CaO produces a hydrogen-rich product gas, and a regenerator in which the sorbent is calcined producing a high purity CO₂ gas stream suitable for storage. The LEGS process operates at a pressure of 2.0 MPa and temperatures less than 800 °C and therefore requires a reactive fuel such as brown coal. The brown coal ash and sulfur are purged from the regenerator together with CaO which is replaced by fresh limestone in order to maintain a steady-state CaO carbonation activity (a_ave). Equilibrium calculations show the influence of process conditions and coal sulfur content on the gasifier carbon capture (>95% is possible). Material balance calculations of the core process show that the required solid purge of the sorbent cycle is mainly attributed to the necessary removal of ash and CaSO₄ if the solid purge is used as a pre-calcined feedstock for cement production. The decay in the CaO capture capacity over many calcination–carbonation cycles demands a high sorbent circulation ratio but does not dictate the purge fraction. A thermodynamic analysis of a LEGS-based combined power and cement production process, where the LEGS purge is directly used in the cement industry, results in an electric efficiency of 42% using a state of the art combined cycle.     

The comparison study on the operating condition of gasification power plant with various feedstocks

Gasification technology, which converts fossil fuels into either combustible gas or synthesis gas (syngas) for subsequent utilization, offers the potential of both clean power and chemicals. Especially, IGCC is recognized as next power generation technology which can replace conventional coal power plants in the near future. It produces not only power but also chemical energy sources such as H₂, DME and other chemicals with simultaneous reduction of CO₂. This study is focused on the determination of operating conditions for a 300 MW scale IGCC plant with various feedstocks through ASPEN plus simulator. The input materials of gasification are chosen as 4 representative cases of pulverized dry coal (Illinois#6), coal water slurry, bunker-C and naphtha. The gasifier model reflects on the reactivity among the components of syngas in the gasification process through the comparison of syngas composition from a real gasifier. For evaluating the performance of a gasification plant from developed models, simulation results were compared with a real commercial plant through approximation of relative error between real operating data and simulation results. The results were then checked for operating characteristics of each unit process such as gasification, ash removal, acid gas (CO₂, H₂S) removal and power islands. To evaluate the performance of the developed model, evaluated parameters are chosen as cold gas efficiency and carbon conversion for the gasifier, power output and efficiency of combined cycle. According to simulation results, pulverized dry coal which has 40.93% of plant net efficiency has relatively superiority over the other cases such as 33.45% of coal water slurry, 35.43% of bunker-C and 30.81% of naphtha for generating power in the range of equivalent 300 MW.     

Techno-economic evaluation of a PVAm CO2-selective membrane in an IGCC power plant with CO2 capture

Published data for an operating power plant, the ELCOGAS 315 MWe Puertollano plant, has been used as a basis for the simulation of an integrated gasification combined cycle process with CO₂ capture. This incorporated a fixed site carrier polyvinylamine membrane to separate the CO₂ from a CO-shifted syngas stream. It appears that the modified process, using a sour shift catalyst prior to sulphur removal, could achieve greater than 85% CO₂ recovery at 95 vol% purity. The efficiency penalty for such a process would be approximately 10% points, including CO₂ compression. A modified plant with CO₂ capture and compression was calculated to cost €2320/kW, producing electricity at a cost of 7.6 € cents/kWh and a CO₂ avoidance cost of about €40/tonne CO₂.     

Application of engineered natural ores to intermediate- and high-temperature CO2 capture and conversion

Integrated CO₂ capture and conversion (ICCC) is a promising technology aiming at converting waste CO₂ to fuels and high value-added chemicals. Herein, we described a proof-of-concept study of applying engineered natural ores (dolomite, magnesite, and limestone) to two different ICCC processes—intermediate-temperature ICCC for CH₄ production (350–400°C) and high-temperature ICCC for syngas production (650–700°C). In the former process, a MgO-based CO₂ sorbent prepared from dolomite and magnesite was combined with a methanation catalyst in a dual-bed configuration, whereby a CH₄ yield of 7.1–7.3 mmol/g can be stably achieved per cycle over 20 consecutive ICCC cycles. In the latter process, a CaO-based sorbent derived from dolomite and limestone was coupled with a reforming catalyst also in a dual-bed mode, whereby syngas with a H₂/CO ratio of 0.9–1.0 can be produced over 20 cycles. This study will expand the application of natural ores in CO₂ emission reduction.