Exergy analysis of hydrogen production from steam gasification of biomass: A review

Exergy analysis of hydrogen production from steam gasification of biomass was reviewed in this study. The effects of the main parameters (biomass characteristics, particle size, gasification temperature, steam/biomass ratio, steam flow rate, reaction catalyst, and residence time) on the exergy efficiency were presented and discussed. The results show that the exergy efficiency of hydrogen production from steam gasification of biomass is mainly determined by the H₂ yield and the chemical exergy of biomass. Increases in gasification temperatures improve the exergy efficiency whereas increases in particle sizes generally decrease the exergy efficiency. Generally, both steam/biomass ratio and steam flow rate initially increases and finally decreases the exergy efficiency. A reaction catalyst may have positive, negative or negligible effect on the exergy efficiency, whereas residence time generally has slight effect on the exergy efficiency.     

Hydrogen production by supercritical water gasification of biomass: Explore the way to maximum hydrogen yield and high carbon gasification efficiency

Supercritical water gasification (SCWG) is a promising technology for wet biomass utilization. In this paper, orthogonal experimental design method, which can minimize the number of experiments compared with the full factorial experiments, was used to optimize the operation parameters of SCWG with a tubular reactor system. Using this method, the influences of the main parameters including pressure, temperature, residence time and solution concentration on biomass gasification were also investigated. Simultaneously, in order to further improve the gasification efficiency of biomass, acid hydrolysis pretreatment of feedstock, oxidizers addition and increasing reaction temperature were employed. Results from the experiments show that in the range of experimental parameters, the order of the effects of the factors on H₂ yield of corn cob gasification in SCW is temperature > pressure > feedstock concentration > residence time. Temperature and pressure have a significant and complicated effect on biomass gasification. Hydrogen yield increases by the acid hydrolysis pretreatment of feedstock, and oxidizer addition reduces the hydrogen yield but it promotes the increase in carbon gasification efficiency. Biomass feedstock with high concentration was gasified successfully at high reaction temperature.     

Hydrogen production by sewage sludge gasification in supercritical water with a fluidized bed reactor

In this work, gasification of sewage sludge in supercritical water was investigated in a fluidized bed reactor. Effect of operating parameters such as temperature, concentration of the feedstock, alkali catalysts and catalyst loading on gaseous products and carbon distribution were systematically studied. The results showed that the increase of temperature and the decrease of feedstock concentration were both favorable for gasification, and the addition of catalyst enhanced the formation of hydrogen better. The K₂CO₃ catalyst could better enhance gasification efficiency and the catalytic activity of different catalysts for hydrogen production was in the following order: KOH > K₂CO₃ > NaOH > Na₂CO_3. The maximum molar fraction and yield of hydrogen reached to 55.96% and 15.49 mol/kg respectively with KOH at 540 °C. Most carbon in feedstock existed in gaseous and liquid products, and alkali catalysts mainly promoted the water-gas shift reaction rather than steam reforming.     

Energy and exergy analysis of biomass gasification at different temperatures

Biomass is usually gasified above the optimal temperature at the carbon-boundary point, due to the use of different types of gasifiers, gasifying media, clinkering/slagging of bed material, tar cracking, etc. This paper is focused on air gasification of biomass with different moisture at different gasification temperatures. A chemical equilibrium model is developed and analyses are carried out at pressures of 1 and 10 bar with the typical biomass feed represented by CH_1.4O_0.59N_0.0017. At the temperature range 900–1373 K, the increase of moisture in biomass leads to the decrease of efficiencies for the examined processes. The moisture content of biomass may be designated as “optimal” only if the gasification temperature is equal to the carbon-boundary temperature for biomass with that specific moisture content. Compared with the efficiencies based on chemical energy and exergy, biomass feedstock drying with the product gas sensible heat is less beneficial for the efficiency based on total exergy. The gasification process at a given gasification temperature can be improved by the use of dry biomass and by the carbon-boundary temperature approaching the required temperature with the change of gasification pressure or with the addition of heat in the process.     

Solar-driven steam-based gasification of sugarcane bagasse in a combined drop-tube and fixed-bed reactor – Thermodynamic,kinetic, and experimental analyses

Syngas production via steam-based thermochemical gasification of Brazilian sugarcane bagasse, using concentrated solar energy for process heat, was thermodynamically and experimentally investigated. Energy and exergy analyses revealed the potential benefits of solar-driven over conventional autothermal gasification that included superior quality of syngas composition and higher yield per unit of feedstock. Reaction rates for the gasification of fast pyrolyzed bagasse char were measured by thermogravimetric analysis and a rate law based on the oxygen exchange mechanism was formulated. In order to provide residence times long enough for adequate char conversion, a laboratory-scale entrained flow reactor that combines drop-tube and fixed-bed concepts was developed. Testing was performed in an electric furnace with the final aim to supply heat by concentrated solar radiation. Experimental runs at reactor temperatures of 1073–1573 K and a biomass feed rate of 0.48 g/min yielded high-quality syngas of molar ratios H₂/CO = 1.6 and CO₂/CO = 0.31, and with heating values of 15.3–16.9 MJ/kg, resulting in an upgrade factor (ratio of heating value of syngas produced over that of the feedstock) of 112%. Theoretical upgrade factors of up to 126%, along with the treatment of wet feedstock and elimination of the air separation unit, support the potential benefits of solar-driven over autothermal gasification.     

Hydrothermal co-gasification of sorghum biomass and çan lignite in mild conditions: An optimization study for high yield hydrogen production

In this study, response surface methodology (RSM) combined with a 3–factor and 3–level Box–Behnken design (BBD) was performed to obtain high yield hydrogen production from hydrothermal co–gasification of sorghum biomass and low rank Çan lignite in a batch type reactor at 500 °C. The individual and the combined effects of the process parameters of coal amount (%) of the coal/biomass mixtures, initial water volume (mL) of the reactor and amount of the coal/biomass mixtures (kg) on system pressure, total gas yield, hydrogen production and product distribution were determined. Water volume directly affected the system pressure and the reaction medium was supercritical water medium above 48.2 mL with a pressure of 22.06 MPa. The highest values of both total gas volume and hydrogen gas volume were reached by gasification of 5.0 g of feedstock. It has been observed that total gas volume and hydrogen volume were directly affected by the water volume in the reactor and the coal ratio of the coal-biomass mixtures. The highest total gas and hydrogen volumes can be achieved under the conditions where the higher levels of water volume of the reactor and lower levels of coal percentage of the coal/biomass mixture were combined. Optimum conditions for maximum hydrogen production with 5.0 g of coal/biomass mixture were determined with numerical optimization as coal percentage of 25.6% and initial water volume of 68.5 mL. By combining the impregnated K₂CO₃ (3%, (w/w)) and CaO catalysts an excellent hydrogen selectivity was achieved. The hydrogen selectivity was drastically increased from 32.0% to 70.8% by capturing more than 99% of CO₂ with a H₂/CO₂ mol ratio of 88.5.     

Hydrogen production from glycerol by supercritical water gasification in a continuous flow tubular reactor

In this work, glycerol was used for hydrogen production by supercritical water gasification. Experiments were conducted in a continuous flow tubular reactor at 445∼600 °C, 25 MPa, with a short residence time of 3.9∼9.0 s. The effects of reaction temperature, residence time, glycerol concentration and alkali catalysts on gasification were systematically studied. The results showed that the gasification efficiency increased sharply with increasing temperature above 487 °C. A short residence time of 7.0 s was enough for 10 wt% glycerol gasification at 567 °C. With the increase of glycerol concentration from 10 to 50 wt%, the gasification efficiency decreased from 88% to 71% at 567 °C. The alkali catalysts greatly enhanced water-gas shift reaction and the hydrogen yield in relation to catalysts was in the following order: NaOH > Na₂CO₃>KOH > K₂CO₃. The hydrogen yield of 4.93 mol/mol was achieved at 526 °C with 0.1 wt% NaOH. No char or tar was observed in all experiments. The apparent activation energy and apparent pre-exponential factor for glycerol carbon gasification were obtained by assuming pseudo first-order kinetics.     

Performance assessment of hydrogen production from a solar-assisted biomass gasification system

In this study, we investigate a solar-assisted biomass gasification system for hydrogen production and assess its performance thermodynamically using actual literature data. We also analyze the entire system both energetically and exergetically and evaluate its performance through both energy and exergy efficiencies. Three feedstocks, namely beech charcoal, sewage sludge and fluff, are considered as samples in the same reactor. While energy efficiencies vary from 14.14% to 27.29%, exergy efficiencies change from 10.43% to 23.92%. We use a sustainability index (SI), as a function of exergy efficiency, to calculate the impacts on sustainable development and environment. This index changes from 1.12 to 1.31 due to intensive utilization of solar energy. Also, environmental impact of these systems is evaluated through calculating the specific greenhouse gas (GHG) emissions. They are determined to be 17.97, 17.51 and 26.74 g CO₂/MJ H₂ for beech charcoal, sewage sludge and fluff, respectively.     

Hydrogen production from low temperature supercritical water Co-Gasification of low rank lignites with biomass

Co–gasification of low rank lignite (Çan) with sorghum energy crop was investigated under low temperature conditions with supercritical water (773 K, 26.9 MPa). The effects of the water volume in the reactor, blending ratios of the coal/sorghum mixtures, the use of different catalysts, and the variation of feedstock concentrations on the gasification efficiency, product distribution, and hydrogen yields were evaluated. Synergistic effects were observed for both the gasification efficiency and the hydrogen yield with a coal content of 25 wt% in the coal/biomass mixture. Increasing the initial water volume, decreasing the feedstock concentration, and using the alkali metal catalysts Na₂CO₃ and K₂CO₃ significantly increased the gasification efficiency and the hydrogen yield. In experiments with CaO, almost all the carbon dioxide formed was isolated from the gas product during gasification, and the hydrogen yield was more than 70%. The liquid products were mainly composed of alkylphenols and their derivatives.     

Exergy analysis of hydrogen production plants based on biomass gasification

Biomass gasification is a promising option for the sustainable production of hydrogen rich gas. Five different commercial or pilot scale gasification systems are considered for the design of a hydrogen production plant that generates almost pure hydrogen. For each of the gasification technique models of two different hydrogen production plants are developed in Cycle-Tempo: one plant with low temperature gas cleaning (LTGC) and the other with high temperature gas cleaning (HTGC). The thermal input of all plants is 10 MW of biomass with the same dry composition. An exergy analysis of all processes has been made. The processes are compared on their thermodynamic performance (hydrogen yield and exergy efficiency). Since the heat recovery is not incorporated in the models, two efficiencies are calculated. The first one is calculated for the case that all residual heat can be applied, the case with ideal heat recovery, and the other is calculated for the case without heat recovery. It is expected that in real systems only a part of the residual heat can be used. Therefore, the actual value will be in between these calculated values. It was found that three processes have almost the same performance: The Battelle gasification process with LTGC, the FICFB gasification process with LTGC, and the Blaue Turm gasification process with HTGC. All systems include further processing of the cleaned gas from biomass gasification into almost pure hydrogen. The calculated exergy efficiencies are, respectively, 50.69%, 45.95%, and 50.52% for the systems without heat recovery. The exergy efficiencies of the systems with heat recovery are, respectively, 62.79%, 64.41%, and 66.31%. The calculated hydrogen yields of the three processes do not differ very much. The hydrogen yield of the Battelle LTGC process appeared to be 0.097 kg (kg_{(dry biomass)})⁻¹, for the FICFB LTGC process a yield of 0.096 kg (kg_{(dry biomass)})⁻¹ was found, and for the Blaue Turm HTGC 0.106 kg (kg_{(dry biomass)})⁻¹.     

A review on biomass‐based hydrogen production and potential applications

In this paper, a detailed review is presented to discuss biomass‐based hydrogen production systems and their applications. Some optimum hydrogen production and operating conditions are studied through a comprehensive sensitivity analysis on the hydrogen yield from steam biomass gasification. In addition, a hybrid system, which combines a biomass‐based hydrogen production system and a solid oxide fuel cell unit is considered for performance assessment. A comparative thermodynamic study also is undertaken to investigate various operational aspects through energy and exergy efficiencies. The results of this study show that there are various key parameters affecting the hydrogen production process and system performance. They also indicate that it is possible to increase the hydrogen yield from 70 to 107 g H₂ per kg of sawdust wood. By studying the energy and exergy efficiencies, the performance assessment shows the potential to produce hydrogen from steam biomass gasification. The study further reveals a strong potential of this system as it utilizes steam biomass gasification for hydrogen production. To evaluate the system performance, the efficiencies are calculated at particular pressures, temperatures, current densities, and fuel utilization factors. It is found that there is a strong potential in the gasification temperature range 1023–1423 K to increase energy efficiency with a hydrogen yield from 45 to 55% and the exergy efficiency with hydrogen yield from 22 to 32%, respectively, whereas the exergy efficiency of electricity production decreases from 56 to 49.4%. Hydrogen production by steam sawdust gasification appears to be an ultimate option for hydrogen production based on the parametric studies and performance assessments that were carried out through energy and exergy efficiencies. Finally, the system integration is an attractive option for better performance. Copyright © 2012 John Wiley & Sons, Ltd.     

A Life Cycle Analysis on a Bio-DME production system considering the species of biomass feedstock in Japan and Papua New Guinea

This paper describes the performance and/or CO₂ intensities of a Bio-DME (Biomass Di-methyl Ether) production system, considering the differences of biomass feedstock. In the past LCA studies on an energy chain model, there is little knowledge on the differences of biomass feedstock and/or available condition. Thus, in this paper, we selected Papua New Guinea (PNG) which has good potential for supply of an energy crop (a short rotation forestry), and Japan where wood remnants are available, as model areas. Also, we referred to 9 species of biomass feedstock of PNG, and to 8 species in Japan.The system boundary on our LCA consists of (1) the pre-treatment process, (2) the energy conversion process, and (3) the fuel transportation process. Especially, since the pre-treatment process has uncertainties related to the moisture content of biomass feedstock, as well as the distance from the cultivation site to the energy plant, we considered them by the Monte Carlo simulation.Next, we executed the process design of the Bio-DME production system based on the basic experimental results of pyrolysis and char gasification reactions. Due to these experiments, the gas components of pyrolysis and the gasification rate under H₂O (steam) and CO₂ were obtained. Also, we designed the pressurized fluid-bed gasification process. In a liquefaction process, that is, a synthesis process of DME, the result based on an equilibrium constant was used. In the proposed system, a steam turbine for an auxiliary power was assumed to be equipped, too. The energy efficiencies are 39.0–56.8 LHV-%, depending upon the biomass species.Consequently, CO₂ intensities in the whole system were 16.3–47.2 g-CO₂/MJ-DME in the Japan case, and 12.2–36.7 g-CO₂/MJ-DME in the PNG one, respectively.Finally, using the results of CO₂ intensities and energy efficiencies, we obtained the regression equations as parameters of hydrogen content and heating value of a feedstock. These equations will be extremely significant when we install the BTL (biomass-to-liquid, ex. Bio-DME) energy system in the near future, in order to mitigate CO₂ emissions effectively, and to estimate the energy’s efficiency.     

Hydrogen production from steam gasification of tableted biomass in molten eutectic carbonates

The steam gasification of tableted biomass for H₂ production in molten salts was investigated under different conditions. The results showed that the ternary molten carbonates (32 wt% Li₂CO₃, 33 wt% Na₂CO₃ and 35 wt% K₂CO₃) acted as heat medium and catalyst in the gasification process. The use of molten salts could significantly increase total gas and H₂ production and simultaneously decrease the concentrations of CO and CH₄ in the product gas, and also decrease the yield of condensable tar. The increase in gasification temperature and mass ratio of steam to biomass (S/B) was beneficial for H₂ production process. However, excessive steam contributed slightly to the increase in H₂ production and largely increased the energy consumption. The optimal S/B ratio was found to be 1.0. The feedstock after tabletting could completely immersed in molten salts, which improved the contact between biomass and molten salts and thus favored the biomass gasification for H₂ production. When biomass particle size was 0.25 g/piece, the yield of H₂ reached 807.53 mL/g biomass.     

Experimental study on the energy conversion of food waste via supercritical water gasification: Improvement of hydrogen production

In this study, the model food waste was gasified to hydrogen-rich syngas in a batch reactor under supercritical water condition. The model food consisted of rice, chicken, cabbage, and cooking oil. The effects of the main operating parameters including temperature (420–500 °C), residence time (20–60 min) and feedstock concentration (2–10 wt%) were investigated. Under the optimal condition at 500 °C, 2 wt% feedstock and 60 min residence time, the highest H₂ yield of 13.34 mol/kg and total gas yield of 28.27 mol/kg were obtained from non-catalytic experiments. In addition, four commercial catalysts namely FeCl₃, K₂CO₃, activated carbon, and KOH were employed to investigate the catalytic effect of additives at the optimal condition. The results showed that the highest hydrogen yield of 20.37 mol/kg with H₂ selectivity of 113.19%, and the total gas yield of 38.36 mol/kg were achieved with 5 wt% KOH addition Moreover, the low heating value of gas products from catalytic experiments with KOH increased by 32.21% compared to the non-catalytic experiment. The catalytic performance of the catalysts can be ranked in descending order as KOH > activated carbon > FeCl₃ > K₂CO₃. The supercritical water gasification (SCWG) with KOH addition can be a potential applied technology for food waste treatment with production of hydrogen-rich gases.     

Sustainable hydrogen production options and the role of IAHE

In this paper, some potential sustainable hydrogen production options are identified and discussed. There are natural resources from which hydrogen can be extracted such as water, fossil hydrocarbons, biomass and hydrogen sulphide. In addition, hydrogen can be extracted from a large palette of anthropogenic wastes starting with biomass residuals, municipal wastes, plastics, sewage waters etc. In order to extract hydrogen from these resources one needs to use sustainable energy sources like renewables and nuclear. A total of 24 options for sustainable hydrogen production are then identified. Sustainable water splitting is the most important method of hydrogen production. Five sustainable options are discussed to split water, which include electrolysis, high temperature electrolysis, pure and hybrid thermochemical cycles, and photochemical/radiochemical methods. Other 19 methods refer to extraction of hydrogen from other materials than water or in conjunction with water (e.g., coal gasification with CO₂ capture and sequestration). For each case the achievable energy and exergy efficiency of the method were estimated based on state of the art literature screening for each involved process. In addition, a range of hydrogen production capacity is determined for each of the option. For a transition period to hydrogen economy nuclear or solar assisted coal gasification and fossil fuel reforming technologies – with efficiencies of 10–55% including CO₂ sequestration – should be considered as a viable option. Other “ready to be implemented” technology is hydro-power coupled to alkaline electrolysers which shows the highest hydrogen generation efficiency amongst all electrical driven options with 60–65%. Next generation nuclear reactors as to be coupled with thermochemical cycles have the potential to generate hydrogen with 40–43% energy efficiency (based on LHV of hydrogen) and 35–37% exergy efficiency (based on chemical exergy of hydrogen). Furthermore, recycling anthropogenic waste, including waste heat, waste plastic materials, waste biomass and sewage waters, shows also good potential as a sustainable option for hydrogen production. Biomass conversion to hydrogen is found as potentially the most efficient amongst all studied options in this paper with up to 70% energy efficiency and 65% exergy efficiency.     

Thermodynamic analysis of hydrogen rich synthetic gas generation from fluidized bed gasification of rice husk

In the present work, the generation of hydrogen rich synthetic gas from fluidized bed steam gasification of rice husk has been studied. An equilibrium model based on equilibrium constant and material balance has been developed to predict the gas compositions. The equilibrium gas compositions are compared with the experimental data of the present group as well as of available literature. The energy and exergy analysis of the process have been carried out by varying steam to biomass ratio (ψ) within the range between 0.1-1.5 and gasification temperature from 600 °C to 900 °C. It is observed that both the energy and exergy efficiencies are maximum at the CBP (carbon boundary point) though the hydrogen production increases beyond the CBP. The HHV (higher heating value) and the external energy input both continuously increase with ψ. However, the hydrogen production initially increases with increase in temperature up to 800 °C and then becomes nearly asymptotic. The HHV decreases rapidly with increase in temperature and energy input increases. Therefore, gasification in lower temperature region is observed to be economical in terms of a trade off between external energy input and HHV of the product gas.     

Exergy evaluation of biomass steam gasification via interconnected fluidized beds

This paper presents the thermodynamic assessment of biomass steam gasification via interconnected fluidized beds (IFB) system. The performance examined included the composition, yield and higher heating value (HHV) of dry syngas, and exergy efficiencies of the process. Two exergy efficiencies were calculated for the cases with and without heat recovery, respectively. The effects of steam‐to‐biomass ratio (S/B), gasification temperature, and pressure on the thermodynamic performances were investigated based on a modified modeling of the IFB system. The results showed that at given gasification temperature and pressure, the exergy efficiencies and dry syngas yield reached the maximums when S/B was at the corresponding carbon boundary point (S/B_CBP). The HHV of the dry syngas continuously decreased with the increase of S/B. Moreover, the exergy efficiency with heat recovery was averagely a dozen percentage points higher than that without heat recovery. Under atmospheric conditions, lower gasification temperature favored the yield and HHV of dry syngas at various S/B. In addition, it also favored the exergy efficiencies of the process when S/B is approximately larger than 0.75. Under pressurized conditions, higher gasification pressure favored both the yield and HHV of dry syngas, as well as the exergy efficiencies at different S/B. Copyright © 2013 John Wiley & Sons, Ltd.     

Exergy analysis of biomass-to-synthetic natural gas (SNG) process via indirect gasification of various biomass feedstock

This paper presents an exergy analysis of SNG production via indirect gasification of various biomass feedstock, including virgin (woody) biomass as well as waste biomass (municipal solid waste and sludge). In indirect gasification heat needed for endothermic gasification reactions is produced by burning char in a separate combustion section of the gasifier and subsequently the heat is transferred to the gasification section. The advantages of indirect gasification are no syngas dilution with nitrogen and no external heat source required. The production process involves several process units, including biomass gasification, syngas cooler, cleaning and compression, methanation reactors and SNG conditioning. The process is simulated with a computer model using the flow-sheeting program Aspen Plus. The exergy analysis is performed for various operating conditions such as gasifier pressure, methanation pressure and temperature. The largest internal exergy losses occur in the gasifier followed by methanation and SNG conditioning. It is shown that exergetic efficiency of biomass-to-SNG process for woody biomass is higher than that for waste biomass. The exergetic efficiency for all biomass feedstock increases with gasification pressure, whereas the effects of methanation pressure and temperature are opposite for treated wood and waste biomass.     

Absorption-enhanced steam gasification of biomass for hydrogen production: Effect of calcium oxide addition on steam gasification of pyrolytic volatiles

The effect mechanism of calcium oxide (CaO) addition on gasification of pyrolytic volatiles as a key sub-process in the absorption-enhanced steam gasification of biomass (AESGB) for H₂ production at different conditions was investigated using a two-stage fixed-bed pyrolysis–gasification system. The results indicate that CaO functions as a CO₂ absorbent and a catalyst in the volatiles gasification process. CaO triggers the chemical equilibrium shift to produce more H₂ and accelerates volatile cracking and gasification reactions to obtain high volatile conversion rates. Increasing the gasification temperature could improve the reaction rate of cracking and gasification of volatiles as well as the catalytic effect of CaO, which continuously increase H₂ yield. When the gasification temperature exceeds 700 °C, the sharp decrease in CO₂ absorption capability of CaO drastically increases the CO₂ concentration and yield, which significantly decrease H₂ concentration. The appropriate temperature for the absorption-enhanced gasification process should be selected between 600 °C and 700 °C in atmospheric pressure. Increasing the water injection rate (represented as the mass ratio of steam to biomass) could also improve H₂ yield. The type of biomasses is closely associated with H₂ yield, which is closely related to the volatile content of biomass materials.     

Exergy analysis of biomass staged-gasification for hydrogen-rich syngas

Using Aspen Plus simulations, exergy analyses of hydrogen-rich syngas production via biomass staged-gasification are carried out for three configurations, namely, staged-gasification with pyrolysis gas combustion and char gasification (C-1), staged-gasification with pyrolysis gas reforming and char gasification (C-2), and staged-gasification with pyrolysis gas reforming and char combustion (C-3). The results show that, for the gasification and reforming processes, the exergy loss of pyrolysis gas with tar reforming is less than that of char gasification. As for the system, it is conducive to generating hydrogen by making full use of the hydrogen element (H) in biomass instead of the H in water. The benefits of C-1 are that it removes tar and produces higher yield and concentration of hydrogen. However, C-2 is capable of obtaining higher exergy efficiency and lower exergy loss per mole of H₂ production. C-3 theoretically has greater process performances, but it has disadvantages in tar conversion in practical applications. The appropriate gasification temperature (T_G) are in the range of 700–750 °C and the appropriate mass ratio of steam to biomass (S/B) are in the range of 0.6–0.8 for C-1 and C-3; the corresponding parameters for C-2 are in the ranges of 650–700 °C and 0.7–0.8, respectively.