Biohythane as an energy feedstock for solid oxide fuel cells

Biogas (60%-CH₄, 40%- CO₂) is a potential source of renewable energy when used as energy feedstock for solid oxide fuel cells (SOFC), but releases biogenic CO₂ emissions. Hybrid SOFC performance can be affected by fuel composition and reformer performance. Biohythane (58%-CH₄, 35%-CO₂ and 7% H₂) can be a better alternative providing balance between energy and biogenic emissions. Biohythane performance is studied for a 120 kW SOFC stack using ASPEN process model and compared with other feed stocks. This work is the first to study and report on the application of biohythane in SOFC systems. Biohythane was found to produce less biogenic CO₂ emissions and 6% less CO at the reformer than biogas. Comparisons show that biohythane provides better efficiencies in hybrid SOFC systems. Sensitivity studies recommends operation of stack with biohythane at Steam to Carbon Ratio (STCR) = 2.0, i = 200 mA cm⁻² and U_F = 0.85 respectively.     

Effects of methane processing strategy on fuel composition,electrical and thermal efficiency of solid oxide fuel cell

Natural gas is a cheap and abundant fuel for solid oxide fuel cell (SOFC), generally integrating the SOFC system with methane pre-treating system for improving the stability of SOFC. In this paper, the accurate effects of methane processing strategy on fuel composition, electrical efficiency and thermal efficiency of SOFC are investigated based on the thermodynamic equilibrium. Steam reforming of methane is an endothermic process and can produce 3 mol of H₂ and 1 mol of CO from 1 mol of methane, and thus the electrical efficiency of SOFC is high at the same O/C ratio and equivalent fuel utilization, whereas the thermal efficiency is low. On the contrary, partial oxidation of methane is an exothermal process and only produces 2 mol of H₂ and 1 mol of CO from 1 mol of methane, and thus the electrical efficiency of SOFC is low at the same O/C ratio and equivalent fuel utilization, whereas the thermal efficiency is high. When the O/C ratio is 1.5, the electrical efficiency of SOFC is 55.3% for steam reforming of methane, while 32.7% for partial oxidation of methane. High electrical efficiency of SOFC can be achieved and carbon deposition can be depressed by selecting suitable O/C ratio from methane pretreatment according to the accurate calculation and analysis of effects of different methane processing strategies on the electrical efficiency and thermal efficiency of SOFC.     

Combined methane reforming by carbon dioxide and steam in proton conducting solid oxide fuel cells for syngas/power co-generation

Methane and carbon dioxide mixture can be used as the fuel in a proton conducting solid oxide fuel cell (SOFC) for power/syngas co-generation and greenhouse gas reduction. However, carbon deposition and low conversion ratio are potential problems for this technology. Apart from using functional catalytic layer in the SOFC to enhance CH₄ dry reforming, adding H₂O into the fuel stream could facilitate the CH₄ conversion and enhance the co-generation performance of the SOFC. In this work, the effects of adding H₂O to the CO₂CH₄ fuel on the performance of a tubular proton conducting SOFC are studied numerically. Results show that the CH₄ conversion is improved from 0.830 to 0.898 after adding 20% H₂O to the anode. Meanwhile, the current density is increased from 2832 A m⁻² to 3064 A m⁻² at 0.7 V. Sensitivity studies indicate that the H₂:CO ratio can be effectively controlled by the amount of H₂O addition and the H₂ starvation can be alleviated, especially at high current density conditions.     

Is steam addition necessary for the landfill gas fueled solid oxide fuel cells?

Landfill gas in Hong Kong – a mixture of about 50% (by volume) CH₄ and 50% CO₂ – can be utilized for power generation in a solid oxide fuel cell (SOFC). Conventional way of utilizing CH₄ in a SOFC is by adding H₂O to CH₄ to initiate methane steam reforming (MSR) and water gas shift reaction (WGSR). As the methane carbon dioxide reforming (MCDR: CH₄ + CO₂ ↔ 2CO + 2H₂) is feasible in the SOFC anode, it is unknown whether H₂O is needed or not for landfill gas fueled SOFC. In this study, a numerical model is developed to investigate the characteristics of SOFC running on landfill gas. Parametric simulations show that H₂O addition may decrease the performance of short SOFC at typical operating conditions as H₂O dilute the fuel concentration. However, it is interesting to find that H₂O addition is needed at reduced operating temperature, lower operating potential, or in SOFC with longer gas channel, mainly due to less temperature reduction in the downstream and easier oxidation of H₂ than CO. This preliminary study could help identify strategies for converting landfill gas into electrical power in Hong Kong.     

Methane-free biogas for direct feeding of solid oxide fuel cells

This paper deals with the experimental analysis of the performance and degradation issues of a Ni-based anode-supported solid oxide fuel cell fed by a methane-free biogas from dark-anaerobic digestion of wastes by pastry and fruit shops. The biogas is produced by means of an innovative process where the biomass is fermented with a pre-treated bacteria inoculum (Clostridia) able to completely inhibit the methanization step during the fermentation process and to produce a H₂/CO₂ mixture instead of conventional CH₄/CO₂ anaerobic digested gas (bio-methane). The proposed biogas production route leads to a biogas composition which avoids the need of introducing a reformer agent into or before the SOFC anode in order to reformate it.In order to analyse the complete behaviour of a SOFC with the bio-hydrogen fuel, an experimental session with several H₂/CO₂ synthetic mixtures was performed on an anode-supported solid oxide fuel cell with a Ni-based anode. It was found that side reactions occur with such mixtures in the typical thermodynamic conditions of SOFCs (650–800 °C), which have an effect especially at high currents, due to the shift to a mixture consisting of hydrogen, carbon monoxide, carbon dioxide and water. However, cells operated with acceptable performance and carbon deposits (typical of a traditional hydrocarbon-containing biogas) were avoided after 50 h of cell operation even at 650 °C. Experiments were also performed with traditional bio-methane from anaerobic digestion with 60/40 vol% of composition. It was found that the cell performance dropped after few hours of operation due to the formation of carbon deposits.A short-term test with the real as-produced biogas was also successfully performed. The cell showed an acceptable power output (at 800 °C, 0.35 W cm⁻² with biogas, versus 0.55 W cm⁻² with H₂) although a huge quantity of sulphur was present in the feeding fuel (hydrogen sulphide at 103 ppm and mercaptans up to 10 ppm). Therefore, it was demonstrated the interest relying on a sustainable biomass processing which produces a biogas which can be directly fed to SOFC using traditional anode materials and avoiding the reformer component since the methane-free mixture is already safe for carbon deposition.     

Experimental study of dry reforming of biogas in a tubular anode-supported solid oxide fuel cell

The performance of a tubular Ni/YSZ anode supported SOFC directly fed by an anaerobic digestion simulated biogas, with an extra addition of carbon dioxide to operate in conservative operating conditions to avoid coking on the anode support, was investigated. The fuel cell has been tested at a fixed oven temperature of 800 °C and under biogas/CO₂ mixtures with different volumetric ratios, fuel utilization (FU) and current densities. Polarization curves and performance maps were obtained to better understand the influence of the investigated operational parameters on the cell behavior. Furthermore, since the tubular geometry enables an easy separation of the anode and cathode exhaust gases, the anode off-gas has been collected and monitored through a gas-chromatograph under open circuit voltage to investigate on the catalytic behavior of a Ni-based state-of-the-art anode. For corresponding operative conditions, performances of the cell for biogas/CO₂ 1/1.5 (i.e. CH₄/CO₂ 30/70) and 1/2 (i.e. CH₄/CO₂ 24/76) were at least 2% and 4% lower than the case 1/1 (i.e. CH₄/CO₂ 20/80), respectively. The highest efficiency of 43.4% was reached at 17.5 A and FU = 70%.     

Recent progress on solid oxide fuel cell: Lowering temperature and utilizing non-hydrogen fuels

A solid oxide fuel cell (SOFC) is a promising energy conversion device with high efficiency and low pollutant emission. The practical application of the conventional SOFCs is limited mainly because of their high operating temperature and the inconvenience brought by the H₂ fuel utilization. This work reviews the recent progress on intermediate temperature SOFCs especially with non-hydrogen fuels. Composite electrolyte consisting of a solid oxide ionic conducting phase and a molten carbonate phase exhibits sufficient ionic conductivity in the intermediate temperature range, i.e. 500–800 °C, and facilitates the simultaneous conduction of H⁺, O²⁻ and CO₃²⁻ ions. A single cell with the composite electrolyte shows a promising power density, 1700 mW cm⁻² at 650 °C with hydrogen as the fuel. The composite electrolyte has been also employed in a direct carbon fuel cell (DCFC), and the simultaneous conduction of O²⁻ and CO₃²⁻ in the electrolyte has been proposed. Recently, perovskite structured materials are found to have good resistance to coke formation as the anode of the direct hydrocarbon solid oxide fuel cell, and several carbon resistant perovskite anodes are employed in all-perovskite structured SOFCs, which exhibit excellent performance with CH₄ and methanol as the fuel.     

Effect of food to microorganisms (F/M) ratio on biohythane production via single-stage dark fermentation

Hythane is a mixture of hydrogen and methane gases which are generally produced in separate ways. This work studied mesophilic biohythane gas (H₂+CH₄+CO₂) production in a bioreactor via single-stage dark fermentation. The fermentation was conducted in batch mode using mixed anaerobic microflora and food waste and condensed molasses fermentation soluble to elucidate the effects of food to microorganisms (F/M) ratio (ranging from 0.2 to 38.2) on gas production, metabolite variation, kinetics and biohythane-composition indicator performances. The experimental results indicate that the F/M ratio and fermentation time affect biohythane production efficiency with values of peak maximum hydrogen production rate 9.60 L/L-d, maximum methane production rate 0.72 L/L-d, and hydrogen yield (HY) of 6.17 mol H₂/kg COD_added. Depending on the F/M ratios, the H₂, CH₄ and CO₂ biogas components were 10–60%, 5–20% and 35–70%, respectively. Prospects for the further real application for single-stage biohythane fermentation based on the experimental data are proposed. This work characterizes an important reactor operation factor F/M ratio for innovative single-stage dark fermentation.     

Effect of pH shock on single-stage biohythane production using gel-entrapped anaerobic microorganisms

A novel single-reactor system having entrapped anaerobic microorganisms has been developed to co-produce H₂ and CH₄. pH is one of the key operating and environmental parameters affecting the performance of a bio-system. This work aimed to investigate the pH shock effects on the novel biohythane system. The experiments were suddenly changing the original cultivation pH value of 6 into 4, 5, 7 or 8 for 4 h. The results indicate that a short pH shock could be used to regulate H₂/CH₄ composition without notably affecting biogas yield and chemical oxygen demand (COD) removal. Peak biohythane production was obtained after the pH shock to 8, having H₂/CH₄ yields of 11.5 ± 1.6/44.8 ± 3.1 mL/g COD. During pseudo steady-state conditions of effective cultivation periods, the values of H₂ content in biohythane and COD removal efficiency were in ranges of 20–39% and 71–79%, respectively. The significances and applications of the experimental results have been discussed. The novelty of this work is elucidating a less-discussed field-operation problem of pH perturbances for a newly-developed biohythane system.     

Investigation of La0.6Sr0.4Co1-xNixO3-δ (x=0, 0.2, 0.4, 0.6, 0.8) catalysts on solid oxide fuel cells anode for biogas dry reforming

The introduction of catalyst on anode of solid oxide fuel cell (SOFC) has been an effective way to alleviate the carbon deposition when utilizing biogas as the fuel. A series of La_0.6Sr_0.4Co_1-xNi_xO_3-δ (x = 0, 0.2, 0.4, 0.6, 0.8) oxides are synthesized by sol-gel method and used as catalysts precursors for biogas dry reforming. The phase structure of La_0.6Sr_0.4Co_1-xNi_xO_3-δ oxides before and after reduction are characterized by X-ray diffraction (XRD). The texture properties, carbon deposition, CH₄ and CO₂ conversion rate of La_0.6Sr_0.4Co_1-xNi_xO_3-δ catalysts are evaluated and compared. The peak power density of 739 mW cm^?2 is obtained by a commercial SOFC with La_0.6Sr_0.4Co_0.4Ni_0.6O_3-δ catalyst at 850 °C when using a mixture of CH₄: CO₂ = 2:1 as fuel. This shows a great improvement from the cell without catalyst for internal dry reforming, which is attributed to the formation of NiCo alloy active species after reduction in H₂ atmosphere. The results indicate the benefits of inhibiting the carbon deposition on Ni-based anode through introducing the La_0.6Sr_0.4Co_0.4Ni_0.6O_3-δ catalyst precursor. Additionally, the dry reforming technology will also help to convert part of the exhaust heat into chemical energy and improve the efficiency of SOFC system with biogas fuel.     

Pilot-scale of biohythane production from palm oil mill effluent by two-stage thermophilic anaerobic fermentation

The pilot-scale of two-stage thermophilic (55 °C) for biohythane production from palm oil mill effluent (POME) was operated at hydraulic retention time (HRT) of 2 days and organic loading rate (OLR) of 27.5 gCOD/L⋅d) for first stage and HRT of 10 days and OLR of 5.5 gCOD/L⋅d for second stage. Biohythane production rate was 1.93 L-gas/L⋅d with biogas containing 11% H₂, 37% CO₂, and 52% CH₄. Recirculation of methane effluent mixed with POME at a ratio of 1:1 can control pH in the first stage at an optimal range of 5.0–6.5. Microbial community in hydrogen stage dominated by Thermoanaerobacterium sp., while methane stage dominated by Methanosarcina sp. The H₂/CH₄ ratio of biohythane was 0.13–0.18 which suitable for vehicle fuel. Biohythane production from POME could be promising cleaner biofuel with flexible and controllable H₂/CH₄ ratio.     

Hydrogen-rich syngas production and carbon dioxide formation using aqueous urea solution in biogas steam reforming by thermodynamic analysis

Biogas is a renewable biofuel that contains a lot of CH₄ and CO₂. Biogas can be used to produce heat and electric power while reducing CH₄, one of greenhouse gas emissions. As a result, it has been getting increasing academic attention. There are some application ways of biogas; biogas can produce hydrogen to feed a fuel cell by reforming process. Urea is also a hydrogen carrier and could produce hydrogen by steam reforming. This study then employes steam reforming of biogas and compares hydrogen-rich syngas production and carbon dioxide with various methane concentrations using steam and aqueous urea solution (AUS) by Thermodynamic analysis. The results show that the utilization of AUS as a replacement for steam enriches the production of H₂ and CO and has a slight CO₂ rise compared with pure biogas steam reforming at a temperature higher than 800 °C. However, CO₂ formation is less than the initial CO₂ in biogas. At the reaction temperature of 700 °C, carbon formation does not occur in the reforming process for steam/biogas ratios higher than 2. These conditions led to the highest H₂, CO production, and reforming efficiency (about 125%). The results can be used as operation data for systems that combine biogas reforming and applied to solid oxide fuel cell (SOFC), which usually operates between 700 °C to 900 °C to generate electric power in the future.     

Valorisation of vegetable market wastes to gas fuel via catalytic hydrothermal processing

Residues of leek, cabbage and cauliflower from the market places as representatives of lignocellulosic biomass were processed via hydrothermal gasification to produce energy fuel. The experiments were carried out in a batch reactor at temperatures 300, 400, 500 and 600 °C and corresponding pressures varying in the range of 7.5–43 MPa. Natural mineral additives trona, dolomite and borax were used as homogenous catalysts to determine their effects on the gasification. More than 70 wt% of carbon in vegetable residue samples were detected in the gas phase after the hydrothermal gasification process at 600 °C. The addition of trona mineral further promoted the gasification reactions and as a result, less than 5 wt% carbon remained in the solid residue at the same temperature, degrading the biomass samples into gas and liquid products. The fuel gas with the highest calorific value was recorded to be 25.6 MJ/Nm³, from the hydrothermal gasification of cabbage at 600 °C, when dolomite was used as the homogeneous catalyst. The liquid products obtained in the aqueous phase were detected as organic acids, aldehydes, ketones, furfurals and phenols. The gas products were consisted of hydrogen, carbon dioxide, methane, and as minors; carbon monoxide and low molecular weight hydrocarbons (ethane, propane, etc.). Above 500 °C, all biomass samples yielded 50–55 vol% of CH₄ and H₂ while the CO₂ composition was around 40 vol% as the gas product.     

Lignite as a fuel for direct carbon fuel cell system

Lignite, also known as brown coal, and char derived from lignite by pyrolysis were investigated as fuels for direct carbon solid oxide fuel cells (DC-SOFC). Experiments were carried out with 16 cm² active area, electrolyte supported solid oxide fuel cell (SOFC), using pulverized solid fuel directly fed to DC-SOFC anode compartment in a batch mode, fixed bed configuration. The maximum power density of 143 mW/cm² was observed with a char derived from lignite, much higher than 93 mW/cm² when operating on a lignite fuel. The cell was operating under electric load until fuel supply was almost completely exhausted. Reloading fixed lignite bed during a thermal cycle resulted in a similar initial cell performance, pointing to feasibility of fuel cell operation in a continuous fuel supply mode. The additional series of experiments were carried out in SOFC cell, in the absence of solid fuels, with (a) simulated CO/CO₂ gas mixtures in a wide range of compositions and (b) humidified hydrogen as a reference fuel composition for all cases considered. The solid oxide fuel cell, operated with 92%CO + 8%CO₂ gas mixture, generated the maximum power density of 342 mW/cm². The fuel cell performance has increased in the following order: lignite (DC-SOFC) < char derived from lignite (DC-SOFC) < CO + CO₂ gas mixture (SOFC) < humidified hydrogen (SOFC).     

Stability and coking of direct-methane solid oxide fuel cells: Effect of CO2 and air additions

This paper concerns the stability of anode-supported solid oxide fuel cells (SOFCs), operated with fuel mixtures of methane–CO₂ and methane–air. Stability, which was evaluated in terms of voltage decrease at constant current density, was affected by coke deposits. Chemically inert anode barrier layers were shown to enhance stability and to slow catalytic endothermic reforming reactions within the Ni–YSZ anode that otherwise caused deleterious temperature variations and cell cracking. Increasing the amount of CO₂ added to CH₄ fuel led to a wider stable operating range, yet had relatively little effect on SOFC performance. Button cells operated at 800 ° C with fuel streams of 75% CH₄ and 25% CO₂ achieved maximum power densities above 1 W/cm². Adding air to methane also increased stability. In the case of air addition, SOFC temperature increased as a consequence of exothermic partial-oxidation reforming chemistry. Models were developed to predict temperature and gas-composition profiles within the button cells. The simulation results were used to assist interpretation of the experimental observations.     

Experimental evaluation of methanol steam reforming reactor heated by catalyst combustion for kW-class SOFC

The distributed power generation of methanol steam reforming reactor combined with solid oxide fuel cell (SOFC) has the characteristics of outstanding economic advantages. In this paper, a methanol steam reforming reactor was designed which integrates catalyst combustion, vaporization and reforming. By catalyst combustion, it can achieve stable operation to supply fuel for kW-class SOFC in real time without additional heating equipment. The optimal operating condition of the reforming reactor is 523–553 K, and the steam to carbon ratio (S/C) is 1.2. To study the reforming performance, methanol steam reforming (MSR), methanol decomposition (MD), water-gas shift (WGS) were considered. Operating temperature is the greatest factor affecting reforming performance. The higher the reaction temperature, the lower the H₂ and CO₂, the higher the CO and the methanol conversion rate. The methanol conversion rate is up to 95.03%. The higher the liquid space velocity (LHSV), the lower the methanol conversion rate, the lowest is 90.7%. The temperature changes of the reforming reactor caused by the load change of stack takes about 30 min to reach new balance. Local hotspots within the reforming reactor lead to an excessive local temperature to test a small amount of CH₄ in the reforming gas. The methanation reaction cannot be ignored at the operating temperature. The reforming gas contains 70–75% H₂, 3–8% CO, 18–22% CO₂ and 0.0004–0.3% CH₄. Trace amounts of C₂H₆ and C₂H₄ are also found in some experiments. The reforming reactor can stably supply the fuel for up to 1125 W SOFC.     

In situ study of a composition of outlet gases from biogas fuelled Solid Oxide Fuel Cell performed by the Fourier Transform Infrared Spectroscopy

The purpose of this study was to develop a method and software based on the Fourier Transform Infrared Spectroscopy for the in-situ, quantitative analysis of the composition of outlet gases from Solid Oxide Fuel Cell (SOFC). The calibration procedure performed at the beginning of the experiment indicated a polynomial dependence between the concentration of a calibrating gas (CO, CO₂, CH₄) and the corresponding integrated absorbance in particular wavenumber ranges. Further, it allowed determining a concentration of CO₂, CO, CH₄ and H₂ in the outlet gas stream of the Ni–YSZ anode supported Direct Internal Reforming-SOFC fuelled by synthetic biogas (mixture of CO₂ and CH₄ in a volume ratio 2:3). The analysis was performed for over 90 h. Based on calculated concentration the conversion rates for both CH₄ and CO₂ gases were calculated, as well as the yields and selectivities of CO and H₂. Also, the carbon balance was determined. In order to predict the direction of particular reforming reactions, a non-equilibrium analysis was performed. Namely, a thermodynamic probability of solid carbon formation was determined based on calculations of carbon activity coefficients. Obtained results indicated degradation of a fuel cell and corresponded well with electrical measurements where a decrease of power density in wet synthetic biogas was observed.     

A new phenomenon of a fuel-free current during intermittent fuel flow over Ni-YSZ anode in direct methane SOFCs

A solid oxide fuel cell (SOFC) test unit was constructed with YSZ electrolyte as the support, and with Ni-YSZ anode (Ni:YSZ = 3:5 in weight) and Pt cathode. Direct methane SOFC operation at 800 °C with 10% CH₄ in argon was carried out. A new phenomenon of the generation of the electrical current without the fuel was observed and termed the fuel-free current. An operation of intermittent methane supply was designed to take advantage of three driving forces, i.e. methane in the gas phase, the deposited carbon at the anode surface, and a deficiency of the bulk lattice-oxygen concentration on the anode side, for the generation of the electrical current. A continuous generation of the electrical current is obtained with a methane pulse of only one-fifth of the total operation time. The operation of intermittent methane flow can reduce or even avoid SOFC deactivation by the carbon deposition; at the same time, the deposited carbon can be fully utilized for the power generation. It was also found that hydrogen from methane has been mostly evolved to the outlet gaseous product and the amount of CO formation is much higher than that of CO₂; the operation of intermittent methane flow can further increase the amount of CO over that of CO₂; these are beneficial for the co-generation of synthesis gas.     

Enhanced hydrogen production by the catalytic alkaline thermal gasification of cellulose with Ni/Fe dual-functional CaO based catalysts

A two-stage system involving alkaline thermal gasification of cellulose with Ca(OH)₂ sorbent and catalytic reforming with Ni/Fe dual-functional CaO based catalysts is proposed and applied to enhance H₂ production and in-situ CO₂ capture. The results show that the H₂ concentration is maximized at a considerably lower temperature (500 °C) than commercialized biomass gasification processes, reducing energy consumption. Sol-gel method is deemed better than impregnation method for its lower cost and higher-concentration H₂ production. Among the prepared catalysts, sol-NiCa catalyst exhibits the best performance in CO₂ absorption, resistance to carbon deposition, and cyclic stability, creating maximum H₂ concentration (79.22 vol%), H₂ yield (27.36 mmol g⁻¹ cellulose), and H₂ conversion (57.61%). Introduction of Ni rather than Fe on the CaO based catalyst promotes steam methane reforming at moderate temperature range of 400–600 °C, generating low contents of CH₄ (5.38 vol%), CO₂ (4.82 vol%), and CO (10.58 vol%).     

Biohythane production in two-stage anaerobic digestion system

Hydrogen (H₂) and methane (CH₄) are the potential alternative energy carriers with autonomous extensive and viable importance. These fuels could complement the advantages, and discard the disadvantages of each other, if produced simultaneously. Considering their complementary properties, co-production of a mixture of H₂ and CH₄ in the form of biohythane in two-stage anaerobic digestion (AD) process is gaining more interest than their individual production. Biohythane is a better transportation fuel than compressed natural gas (CNG) in terms of high range of flammability, reduced ignition temperature as well as time, without nitrous oxide (NOx) emissions, improved engine performance without specific modification, etc. Other than production of biohythane, performing two-stage AD is advantageous over one-stage AD due to short HRT, high energy recovery, high COD removal, higher H₂ and CH₄ yields, and reduced carbon dioxide (CO₂) in biogas. For improved biohythane production, various aspects of two-stage AD need to be emphasized. Keeping the facts in mind, the process of two-stage AD along with microbial diversity in comparison to one-stage AD has been discussed in the previous sections of this review. For large scale commercial production, and utilization of biohythane in automobile sector, its execution needs evaluation of process parameters, and problems associated with two-stage AD. Hence, the later part of this review describes the production process of biohythane, concerned microbial diversity, operational process parameters, major challenges and their solutions, applications, and economic evaluation for enhanced production of biohythane.