Integrated gasification combined cycle and carbon capture: A risky option to mitigate CO2 emissions of coal-fired power plants

The power sectors of many big economies still rely on coal-fired plants and emit huge amounts of carbon dioxide. Emerging countries like Brazil, China and South Africa plan to expand the use of coal-fired thermal plants in the next decade. Integrated gasification combined cycle (IGCC) is an innovative technology that facilitates the implementation of carbon capture (CC). The present work analyzes the maturity and costs of the IGCC technology, with and without CC, and assesses the effect of the technology risk on its economic viability. Findings show that the inclusion of the risk in the economic analysis of IGCC plants raises the cost of CO₂ avoided from 36 US$/t_CO2 to 106 US$/t_CO2 in the case of Shell Gasifiers and from 39 US$/t_CO2 to 112 US$/t_CO2 in the case of GE Gasifiers. Thus, the introduction of IGCC with CC on a wider scale faces huge uncertainties. The feasibility of these plants will rely heavily on the overcoming of the technology risk. Besides, its implementation in the short run will depend on government incentives to bear with the additional cost incurred in the first-generation plants.     

Hydrogen production from coal gasification for effective downstream CO2 capture

The coal gasification process is used in commercial production of synthetic gas as a means toward clean use of coal. The conversion of solid coal into a gaseous phase creates opportunities to produce more energy forms than electricity (which is the case in coal combustion systems) and to separate CO₂ in an effective manner for sequestration. The current work compares the energy and exergy efficiencies of an integrated coal-gasification combined-cycle power generation system with that of coal gasification-based hydrogen production system which uses water-gas shift and membrane reactors. Results suggest that the syngas-to-hydrogen (H₂) system offers 35% higher energy and 17% higher exergy efficiencies than the syngas-to-electricity (IGCC) system. The specific CO₂ emission from the hydrogen system was 5% lower than IGCC system. The Brayton cycle in the IGCC system draws much nitrogen after combustion along with CO₂. Thus CO₂ capture and compression become difficult due to the large volume of gases involved, unlike the hydrogen system which has 80% less nitrogen in its exhaust stream. The extra electrical power consumption for compressing the exhaust gases to store CO₂ is above 70% for the IGCC system but is only 4.5% for the H₂ system. Overall the syngas-to-hydrogen system appears advantageous to the IGCC system based on the current analysis.     

Structured exergy analysis of an integrated gasification combined cycle (IGCC) plant with carbon capture

In order to identify approaches for integrated gasification combined cycle (IGCC) plant optimization it is necessary to analyse where and why the losses in the process occur. Therefore a structured exergy analysis of an IGCC with carbon capture was performed to identify losses on a plant, subsystem and individual component level.The investigation of the IGCC base case revealed an exergetic efficiency of 40%. Thus, 60% of the whole fuel exergy is lost in the process. On the subsystem level it was found that the major loss contributor is the combined cycle followed by the gas treatment section and the gasification island. Furthermore, it was demonstrated that the significance of the losses is higher in upstream processes than in downstream processes. On the individual component level it is shown that 80% of all exergy losses in the plant are caused by just 4 components. Since two of them are related to the gas conditioning an advanced hot gas clean-up (HGCU) system was proposed which improves exergy efficiency of the IGCC plant by 5.2%-points. However, assuming an ideal IGCC process an exergy efficiency of 54.1% was calculated demonstrating significant potential for further optimization of the technology.     

Sorbent enhanced hydrogen production from steam gasification of coal integrated with CO2 capture

In this work, CO₂ capture and H₂ production during the steam gasification of coal integrated with CO₂ capture sorbent were investigated using a horizontal fixed bed reactor at atmospheric pressure. Four different temperatures (650, 675, 700, and 750 °C) and three sorbent-to-carbon ratios ([Ca]/[C] = 0, 1, 2) were studied. In the absence of sorbent, the maximum molar fraction of H₂ (64.6%) and conversion of coal (71.3%) were exhibited at the highest temperature (750 °C). The experimental results verified that the presence of sorbent in the steam gasification of coal enhanced the molar fraction of H₂ to more than 80%, with almost all CO₂ was fixed into the sorbent structure, and carbon monoxide (CO) was converted to H₂ and CO₂ through the water gas shift reaction. The steam gasification of coal integrated with CO₂ capture largely depended on the reaction temperature and exhibited optimal conditions at 675 °C. The maximum molar fraction of H₂ (81.7%) and minimum CO₂ concentration (almost 0%) were obtained at 675 °C and a sorbent-to-carbon ratio of 2.     

Sulphur impacts during pulverised coal combustion in oxy-fuel technology for carbon capture and storage

The oxy-fuel process is one of three carbon capture technologies which supply CO₂ ready for sequestration - the others being post-combustion capture and IGCC with carbon capture. As yet no technology has emerged as a clear winner in the race to commercial deployment. The oxy-fuel process relies on recycled flue gas as the main heat carrier through the boiler and results in significantly different flue gas compositions. Sulphur has been shown in the study to have impacts in the furnace, during ash collection, CO₂ compression and transport as well as storage, with many options for its removal or impact control. In particular, the effect of sulphur containing species can pose a risk for corrosion throughout the plant and transport pipelines. This paper presents a technical review of all laboratory and pilot work to identify impacts of sulphur impurities from throughout the oxy-fuel process, from combustion, gas cleaning, compression to sequestration with removal and remedial options. An economic assessment of the optimum removal is not considered. Recent oxy-fuel pilot trials performed in support of the Callide Oxy-fuel Project and other pilot scale data are interpreted and combined with thermodynamic simulations to develop a greater fundamental understanding of the changes incurred by recycling the flue gas. The simulations include a sensitivity analysis of process variables and comparisons between air fired and oxy-fuel fired conditions - such as combustion products, SO₃ conversion and limestone addition.     

Gas hydrate formation process for pre-combustion capture of carbon dioxide

In this study, gas hydrate from CO₂/H₂ gas mixtures with the addition of tetrahydrofuran (THF) was formed in a semi-batch stirred vessel at various pressures and temperatures to investigate the CO₂ separation/recovery properties. This mixture is of interest to CO₂ separation and recovery from Integrated Gasification Combine Cycle (IGCC) power plants. During hydrate formation the gas uptake was determined and composition changes in the gas phase were obtained by gas chromatography. The impact of THF on hydrate formation from the CO₂/H₂ was observed. The addition of THF significantly reduced the equilibrium formation conditions. 1.0 mol% THF was found to be the optimum concentration for CO₂ capture based on kinetic experiments. The present study illustrates the concept and provides thermodynamic and kinetic data for the separation/recovery of CO₂ (pre-combustion capture) from a fuel gas (CO₂/H₂) mixture.     

Hydrate-based pre-combustion carbon dioxide capture process in the system with tetra-n-butyl ammonium bromide solution in the presence of cyclopentane

Effects of 0.29 mol% tetra-n-butyl ammonium bromide (TBAB) solution in conjunction with cyclopentane (CP) on the hydrate-based pre-combustion CO₂ capture are investigated by the measurements of the gas uptakes, CO₂ separation efficiencies and induction time of the hydrate formation at the different temperature-pressure conditions. The results show that the volume of the TBAB has an effect on the CO₂ separation and the induction time, and the addition of the CP into the TBAB solution remarkably enhances the CO₂ separation and shortens the induction time. The system with the CP/TBAB solution volume ratio of 5 vol% and TBAB solution/reactor effective volume ratio of 0.54 is optimum to obtain the largest gas uptake and the highest CO₂ separation efficiency at 274.65 K and 4.0 MPa. Compared to the results with tetrahydrofuran (THF) as an additive [1], the gas uptake is enhanced by at least 2 times and the induction time is shortened at least 10 times at the similar temperature-pressure condition. In addition, the CO₂ concentration in the decomposed gas from the hydrate slurry phase reaches approximately 93 mol% after the first-stage separation at 274.65 K and 2.5 MPa. The gas uptakes of more than 80 mol% are obtained after 400 s at the temperature range of 274.65-277.65 K and the pressure range of 2.5-4.5 MPa.     

A review of carbon dioxide capture and utilization by membrane integrated microalgal cultivation processes

The capture of carbon dioxide (CO₂) from the air for microalgal cultivation has received increasing interest since it allows advantages that do not only reduce the amount of CO₂ already added to the air, but it is also more economical due to the accessibility of air, there are no regeneration requirements and it is a safe method that can help enhance microalgal growth. In order to capture CO₂ from the air, it is necessary to deal with CO₂ emissions from all sources in an atmosphere. Interestingly, the capture unit and microalgal culture can be located at any favorable site. Although a number of photobioreactors have been proposed with a CO₂ distribution system, the consequence of CO₂ losses is still being ignored. Thus, capturing CO₂ from the air via an integrated separation process in a photobioreactor is required for microalgal cultivation. Among the four available separation technologies, the membrane separation process would offer a safe, reliable and low cost method for CO₂ capture. Thus, this method of separation can be considered as a key factor in accelerating the development of a CO₂ enrichment process from the air for microalgal cultivation.     

Enhanced coal gasification heated by unmixed combustion integrated with an hybrid system of SOFC/GT

For clean utilization of coal, enhanced gasification by in situ CO₂ capture has the advantage that hydrogen production efficiency is increased while no energy is required for CO₂ separation. The unmixed fuel process uses a sorbent material as CO₂ carrier and consists of three coupled reactors: a coal gasifier where CO₂ is captured generating a H₂-rich gas that can be utilized in fuel cells, a sorbent regenerator where CO₂ is released by sorbent calcination and it is ready for capture and a reactor to oxidize the oxygen transfer material which produces a high temperature/pressure vitiated air. This technology has the potential to eliminate the need for the air separation unit using an oxygen transfer material. Reactors' temperatures range from 750 °C to 1550 °C and the process operates at pressure around 7.0 bar. This paper presents a global thermodynamic model of the fuel processing concept for hydrogen production and CO₂ capture combined with fuel and residual heat usage. Hydrogen is directly fed to a solid oxide fuel cell and exhaust streams are used in a gas turbine expander and in a heat recovery steam generator. This paper analyzes the influence of steam to carbon ratio in gasifier and regeneration reactor, pressure of the system, temperature for oxygen transfer material oxidation, purge percentage in calciner, average sorbent activity and oxidant utilization in fuel cell. Electrical efficiency up to 73% is reached under optimal conditions and CO₂ capture efficiencies near 96% ensure a good performance for GHG's climate change mitigation targets.     

Recent developments in membrane-based technologies for CO2 capture

Developing new methods and technologies that compete with conventional industrial processes for CO₂ capture and recovery is a hot topic in the current research. Conventional processes do not fit with the current approach of process intensification but take advantage due to their maturity and large-scale implementation. Acting in a precombusion scenario or post-combustion scenario involves the separation of CO₂/H₂ or CO₂/N₂, respectively.     

Technoeconomic assessment of China’s indirect coal liquefaction projects with different CO2 capture alternatives

ICL (Indirect coal liquefaction), an alternative fuel-supplying technology, has drawn much attention and caused considerable debate in China’s energy sector. The hurdles to its development include the high risk of investment into large-scale installations, the high CO₂ emissions and water resource consumption. A comprehensive assessment of ICL is urgently needed. This study provides an economic assessment and a technical analysis based on process simulations. To address the future challenge of curbing CO₂ emissions, three absorption methods are compared for capturing the CO₂ released from the ICL process: DMC (a novel absorbent), MEA and Rectisol. The comparative results suggest that physical absorbents, represented by Rectisol and DMC, have a remarkable advantage over chemical absorption processes, represented by MEA. The Rectisol process costs the least, while the DMC process is close to the same level. As a novel absorbent, DMC has the potential to be widely used in the future. The economic analysis of ICL predicted a high capital cost of over 35 billion yuan and an overall product cost of approximately 3800 yuan/ton for the baseline. In addition, via a sensitivity analysis, coal price, electricity price and capacity factor were identified as the three most influential factors affecting the overall product cost.     

Performance evaluation of integrated gasification solid oxide fuel cell/gas turbine systems including carbon dioxide capture

In this study, system layouts for integrated gasification solid oxide fuel cell/gas turbine (IG-SOFC/GT) systems were proposed and their performance was comparatively evaluated. A baseline IGCC was simulated, and the calculation models were validated. Based on the IGCC system, two IG-SOFC/GT system layouts with different SOFC thermal management methods were established, and their performance was analyzed. The IG-SOFC/GT systems were found to produce much higher power and better efficiency than the IGCC. With regard to SOFC thermal management, the exit gas recirculation scheme showed better performance than the cathode heat exchange scheme. The impact of CO₂ capture was investigated in both the IGCC and IG-SOFC/GT systems, and the penalties in power output and efficiency due to pre-combustion CO₂ capture were found to be milder in the IG-SOFC/GT systems than in the IGCC. An IG-SOFC/GT system adopting oxy-combustion-based CO₂ capture was proposed, and its thermal efficiency was predicted to be sensibly higher than the system with pre-combustion CO₂ capture. Its net power output was predicted to be less than that of the system with pre-combustion technology, but was still much larger than that of the IGCC with pre-combustion CO₂ capture.     

Thermodynamic performance assessment and comparison of IGCC with solid cycling process for CO2 capture at high and medium temperatures

Solid sorbents can be used to capture CO₂ from pre-combustion sources at various temperatures. MgO and CaO are typical medium- and high-temperature CO₂ sorbents. However, pure MgO is not active toward CO₂. The addition of Na₂CO₃ increases the operating temperature and significantly increases the reactivity of sorbents to capture CO₂. Na₂CO₃-promoted MgO is a promising medium-temperature CO₂ sorbent. In this study, the thermodynamic performance of integrated gasification combined cycle (IGCC) systems with Na₂CO₃–MgO-based warm gas decarbonation (WGDC) and CaO-based hot gas decarbonation (HGDC) is evaluated and compared with that of an IGCC system with methyldiethanolamine (MDEA)-based cold gas decarbonation (CGDC). Assuming that the average CO₂ capture capacities of solid sorbents are one-third of their theoretical maxima, we reveal that the IGCC system undergoes approximately 2.8% and 3.6% improvement on net efficiency when switching from CGDC to WGDC and to HGDC, respectively. The net efficiency of the system is increased by improving the CO₂ capture capacity of the sorbent. The IGCC with Na₂CO₃–MgO experiences more significant increase in efficiency than that with CaO along with the improvement of sorbent average CO₂ capture capacity. The efficiency of the IGCC systems reaches the same value when the average CO₂ capture capacities of both sorbents are 53% of their theoretical levels. The effects of gas turbine combustor fuel gas inlet temperature on IGCC system performance are analyzed. Results show that the efficiency of the IGCC systems with HGDC and WGDC increases by 0.74% and 0.53% respectively as the fuel gas inlet temperature increases from 250 °C to 650 °C.     

Combined production of hydrogen and power from heavy oil gasification: Pinch analysis,thermodynamic and economic evaluations

Integrated Gasification Combined Cycle (IGCC) represents a commercially proven technology available for the combined production of hydrogen and electricity power from coal and heavy residue oils. When associated with CO₂ capture and sequestration facilities, the IGCC plant gives an answer to the search for a clean and environmentally compatible use of high sulphur and heavy metal contents fuels, the possibility of installing large size plants for competitive electric power and hydrogen production, and a low cost of CO₂ avoidance.     

Two novel oxy-fuel power cycles integrated with natural gas reforming and CO2 capture

Two novel system configurations were proposed for oxy-fuel natural gas turbine systems with integrated steam reforming and CO₂ capture and separation. The steam reforming heat is obtained from the available turbine exhaust heat, and the produced syngas is used as fuel with oxygen as the oxidizer. Internal combustion is used, which allows a very high heat input temperature. Moreover, the turbine working fluid can expand down to a vacuum, producing an overall high-pressure ratio. Particular attention was focused on the integration of the turbine exhaust heat recovery with both reforming and steam generation processes, in ways that reduce the heat transfer-related exergy destruction. The systems were thermodynamically simulated, predicting a net energy efficiency of 50–52% (with consideration of the energy needed for oxygen separation), which is higher than the Graz cycle energy efficiency by more than 2 percentage points. The improvement is attributed primarily to a decrease of the exergy change in the combustion and steam generation processes that these novel systems offer. The systems can attain a nearly 100% CO₂ capture.     

Biomass-fired cogeneration systems with CO2 capture and storage

In this study, we estimate and analyze the CO₂ mitigation costs of large-scale biomass-fired cogeneration technologies with CO₂ capture and storage. The CO₂ mitigation cost indicates the minimum economic incentive required (e.g. in the form of a carbon tax) to make the cost of a less carbon intensive system equal to the cost of a reference system. If carbon (as CO₂) is captured from biomass-fired energy systems, the systems could in principle be negative CO₂ emitting energy systems. CO₂ capture and storage from energy systems however, leads to reduced energy efficiency, higher investment costs, and increased costs of end products compared with energy systems in which CO₂ is vented. Here, we have analyzed biomass-fired cogeneration plants based on steam turbine technology (CHP-BST) and integrated gasification combined cycle technology (CHP-BIGCC). Three different scales were considered to analyze the scale effects. Logging residues was assumed as biomass feedstock. Two methods were used to estimate and compare the CO₂ mitigation cost. In the first method, the cogenerated power was credited based on avoided power production in stand-alone plants and in the second method the same reference output was produced from all systems. Biomass-fired CHP-BIGCC with CO₂ capture and storage was found very energy and emission efficient and cost competitive compared with other conversion systems.     

Effects of technological learning on future cost and performance of power plants with CO2 capture

This paper demonstrates the concept of applying learning curves in a consistent manner to performance as well as cost variables in order to assess the future development of power plants with CO₂ capture. An existing model developed at Carnegie Mellon University, which had provided insight into the potential learning of cost variables in power plants with CO₂ capture, is extended with learning curves for several key performance variables, including the overall energy loss in power plants, the energy required for CO₂ capture, the CO₂ capture ratio (removal efficiency), and the power plant availability. Next, learning rates for both performance and cost parameters were combined with global capacity projections for fossil-fired power plants to estimate future cost and performance of these power plants with and without CO₂ capture. The results of global learning are explicitly reported, so that they can be used for other purposes such as in regional bottom-up models. Results of this study show that IGCC with CO₂ capture has the largest learning potential, with significant improvements in efficiency and reductions in cost between 2001 and 2050 under the condition that around 3100 GW of combined cycle capacity is installed worldwide. Furthermore, in a scenario with a strict climate policy, mitigation costs in 2030 are 26, 11, 19 €/t (excluding CO₂ transport and storage costs) for NGCC, IGCC, and PC power plants with CO₂ capture, respectively, compared to 42, 13, and 32 €/t in a scenario with a limited climate policy. Additional results are presented for IGCC, PC, and NGCC plants with and without CO₂ capture, and a sensitivity analysis is employed to show the impacts of alternative assumptions on projected learning rates of different systems.     

On the off-design of a natural gas-fired combined cycle with CO2 capture

During the last 15 years cycles with CO₂ capture have been in focus, due to the growing concern over our climate. Often, a natural gas fired combined cycle with a chemical absorption plant for CO₂ capture from the flue gases have been used as a reference in comparisons between cycles. Neither the integration of the steam production for regeneration of amines in the combined cycle nor the off-design behaviour of such a plant has been extensively studied before.     

A comparison of electricity and hydrogen production systems with CO2 capture and storage. Part A: Review and selection of promising conversion and capture technologies

We performed a consistent comparison of state-of-the-art and advanced electricity and hydrogen production technologies with CO₂ capture using coal and natural gas, inspired by the large number of studies, of which the results can in fact not be compared due to specific assumptions made. After literature review, a standardisation and selection exercise has been performed to get figures on conversion efficiency, energy production costs and CO₂ avoidance costs of different technologies, the main parameters for comparison. On the short term, electricity can be produced with 85–90% CO₂ capture by means of NGCC and PC with chemical absorption and IGCC with physical absorption at 4.7–6.9 €ct/kWh, assuming a coal and natural gas price of 1.7 and 4.7 €/GJ. CO₂ avoidance costs are between 15 and 50 €/t CO₂ for IGCC and NGCC, respectively. On the longer term, both improvements in existing conversion and capture technologies are foreseen as well as new power cycles integrating advanced turbines, fuel cells and novel (high-temperature) separation technologies. Electricity production costs might be reduced to 4.5–5.3 €ct/kWh with advanced technologies. However, no clear ranking can be made due to large uncertainties pertaining to investment and O&M costs. Hydrogen production is more attractive for low-cost CO₂ capture than electricity production. Costs of large-scale hydrogen production by means of steam methane reforming and coal gasification with CO₂ capture from the shifted syngas are estimated at 9.5 and 7 €/GJ, respectively. Advanced autothermal reforming and coal gasification deploying ion transport membranes might further reduce production costs to 8.1 and 6.4 €/GJ. Membrane reformers enable small-scale hydrogen production at nearly 17 €/GJ with relatively low-cost CO₂ capture.     

Synergic effect of cyclopentane and tetra-n-butyl ammonium bromide on hydrate-based carbon dioxide separation from fuel gas mixture by measurements of gas uptake and X-ray diffraction patterns

The synergic effect of Cyclopentane (CP) and Tetra-n-butyl Ammonium Bromide (TBAB) on the hydrate-based carbon dioxide (CO₂) separation from IGCC (Integrated Gasification Combined Cycle) syngas is investigated by measuring the gas uptake and the power X-ray diffraction (PXRD) patterns in this work. The CP with CP/TBAB solution ratio of 5 vol% added into the 0.29 mol% TBAB solution can remarkably increase the gas uptake at 4.0 MPa and 274.65 K. The PXRD patterns of the semi-clathrate (sc) hydrate and structure II (sII) hydrate are obtained for the CP/TBAB/gas/H₂O system. The synergic effect of the CP and the TBAB includes two aspects: On one hand, the CP molecules housed in the hollow centers of the large cavities together with TBAB cations (TBA⁺) make the sc hydrate more stable. On the other hand, the TBA⁺ displaced out of the large cavities by the CP molecules make the ionization reaction of TBAB in the solution going toward the reverse direction. Thus, the more TBAB molecules exist in the solution and form the more sc hydrate, resulting in the considerable increase of the gas uptake.