Microbial electrolysis cell powered by an aluminum-air battery for hydrogen generation,in-situ coagulant production and wastewater treatment

Microbial electrolysis cells (MECs) are an efficient technology for generating hydrogen gas from organic matters, but an additional voltage is needed to overcome the thermodynamic barrier of the reaction. A combined system of MEC and the aluminum-air battery (Al-air battery) was designed for hydrogen generation, coagulant production and operated in an energy self-sufficient mode. The Al-air battery (28 mL) produced a voltage ranged from 0.58 V to 0.80 V, which powered an MEC (28 mL) to produce hydrogen. The hydrogen production rate reached 0.19 ± 0.01 m³ H₂/m³/d and 14.5 ± 0.9 mmol H₂/g COD. The total COD removal rate was 85 ± 1%, of which MEC obtained 75 ± 1% COD removal and 10 ± 1% COD removal was achieved by in-situ coagulating process. The microorganisms removal of MEC effluent was 97 ± 2% through ex-situ coagulating process. These results showed that the Al-air battery-MEC system can be operated in energy self-sufficient mode and recovered energy from wastewater with high quality effluent.     

Simultaneous biohydrogen production with distillery wastewater treatment using modified microbial electrolysis cell

The objective of the present study was to construct a compact retrofit design of Microbial Electrolysis Cell (MEC) within an anaerobic digester. In this design, the cathode chamber is inserted in the anodic chamber for compactness, improved hydrogen production and wastewater treatment efficiency. The performance of the new design is compared with that of a conventional (dual chamber) MEC. A cumulative hydrogen of 40.05 ± 0.5 mL and 30.12 ± 0.5 mL were produced at the current density of 811.7 ± 20 and 908.3 ± 25 mA/m² respectively for conventional and modified MEC system. The cathodic hydrogen recovery (CHR) defined as the recovery of electrons as hydrogen which was observed a maximum of 46.5 ± 0.8 and 38.8 ± 0.5% in conventional and modified MEC. The Coulombic efficiency (CE) defined as the recovery of total electrons in acetate as current was observed as 17.25 ± 0.15 and 16.82 ± 0.1% for conventional and modified MEC. In addition, the wastewater COD removal efficiency was observed to be 77.5 ± 1.0% and 75.6 ± 1.5 in 70 h for conventional and modified MEC designs. As shown in the work below, the modified compact design worked effectively to produce hydrogen under different COD concentrations; anolyte and catholyte concentrations; and applied potentials. Thus the modified compact MEC which is also a retrofit to an existing anaerobic digester can extend the use of anaerobic digesters and improve their economics in waste water treatment.     

Influence of catholyte pH and temperature on hydrogen production from acetate using a two chamber concentric tubular microbial electrolysis cell

Microbial electrolysis cells (MECs) could be integrated with dark fermentative hydrogen production to increase the overall system yield of hydrogen. The influence of catholyte pH on hydrogen production from MECs and associated parameters such as electrode potentials (vs Ag/AgCl), COD reduction, current density and quantity of acid needed to control pH in the cathode of an MEC were investigated. Acetate (10 mM, HRT 9 h, 24 °C, pH 7) was used as the substrate in a two chamber MEC operated at 600 mV and 850 mV applied voltage. The effect of catholyte pH on current density was more significant at an applied voltage of 600 mV than at 850 mV. The highest hydrogen production rate was obtained at 850 mV, pH 5 amounting to 200 cm³_stp/l_anode/day (coulombic efficiency 60%, cathodic hydrogen recovery 45%, H₂ yield 1.1 mol/mol acetate converted and a COD reduction of 30.5%). Within the range (18.5–49.4 °C) of temperatures tested, 30 °C was found to be optimal for hydrogen production in the system tested, with the performance of the reactor being reduced at higher temperatures. These results show that an optimum temperature (approximately 30 °C) exists for MEC and that lower pH in the cathode chamber improves hydrogen production and may be needed if potentials applied to MECs are to be minimised.     

Hydrogen gas production with Ni,Ni–Co and Ni–Co–P electrodeposits as potential cathode catalyst by microbial electrolysis cells

The development of efficient and economical cathode, operating at ambient temperature and neutral pH is a crucial challenge for microbial electrolysis cell (MEC) to become commercialize hydrogen production technology. In the present work, eight different electrodes are prepared by the electroplating of Ni, Ni–Co and Ni–Co–P on two base metals i.e., Stainless Steel 316 and Copper separately to use as cathode in MEC. Electrodeposited cathode materials have been characterized by XRD, XPS, FESEM, EDX and linear voltammetry. The fabricated cathodes show higher corrosion stability with improved electro-catalytic performance for the hydrogen production in the MECs as compared to the bare cathodes (SS316 and Cu). Data obtained from linear voltammetry and MEC experiments show that developed cathode possess four times higher intrinsic catalytic activity in comparison to bare cathode. Electrodeposited cathodes are intensively examined in membrane-less MEC, operating under applied voltage of 0.6 V in batch mode at 30 ± 2 °C temperature, in neutral pH with acetate as substrate and activated sludge as inoculum. Ni–Co–P electrodeposit on Stainless Steel 316 cathode gives maximum hydrogen production rate of 4.2 ± 0.5 m³(H₂)m⁻³d⁻¹, columbic efficiencies 96.9 ± 2%, overall hydrogen recovery 90.3 ± 4%, overall energy efficiency 241.2 ± 5%, volumetric current density 310 ± 5 Am⁻³. The net energy recovery and COD removal are 4.25 kJ/gCOD and 61%, respectively. Prepared cathodes show stable performance for continuous 5 batch cycle operations in MEC.     

Anaerobic hydrogen and methane production from low-strength beverage wastewater

In this study, the low-strength effluent from an equalization tank of the wastewater treatment plant in a beverage factory was used for the production of hydrogen and methane. The COD concentration of this low-strength wastewater was 2.9 ± 2.0 g COD/L. In a two-phase anaerobic fermentation system, the hydrogen-producing bioreactor was operated at HRT 8 h, while the methane-producing reactor operated at HRT 24 h. The maximum MPR, methane yield (MY), methane content and COD removal were 72 ± 31 mL/L-d, 58 ± 12 mL/g COD, 92 ± 2% and 78%, respectively. Energy efficiency in this study was calculated as follows, the maximum heating value was 2.2 × 10⁸ kcal/y. The annual carbon-emission reduction was 8.8 × 10⁴ kg CO₂/y, 5.2 × 10⁴ kg CO₂/y, 7.2 × 10⁴ kg CO₂/y when energy-equivalent coal, natural gas or fuel was used, respectively.     

Biohydrogen production from sugar industry effluents using nickel based electrode materials in microbial electrolysis cell

Biohydrogen production from sugar industry effluents in a dual chamber microbial electrolysis cell (MEC) was investigated in this study. The MEC reactor was operated with different effluents as a substrate from cane sugar and raw sugar reprocessing units of sugar industry. The biohydrogen production was investigated using different cathode materials of Nickel plate, Nickel foam, Stainless Steel mesh. The performance of MEC was tested based on the production of hydrogen, coloumbic efficiency, hydrogen recovery and COD removal efficiency respectively. The MEC hydrogen productions revealed that cane sugar effluent was more effective as compared to raw sugar effluent. The experimental results showed that at an applied voltage of 1.0 V, Ni-foam exhibited maximum hydrogen production of 1.59 and 1.43 mmol/L/D in cane sugar and raw sugar effluents respectively, which was about twice than SS-mesh and 1.2 times Ni-plate. This study shows that Ni-foam is one of the potential candidate as low cost electrode for improving hydrogen production in MEC technology with the treatment of industrial effluents.     

Effect of hydraulic retention time on hydrogen production and chemical oxygen demand removal from tapioca wastewater using anaerobic mixed cultures in anaerobic baffled reactor (ABR)

This study evaluated hydrogen production and chemical oxygen demand removal (COD removal) from tapioca wastewater using anaerobic mixed cultures in anaerobic baffled reactor (ABR). The ABR was conducted based on the optimum condition obtained from the batch experiment, i.e. 2.25 g/L of FeSO₄ and initial pH of 9.0. The effects of the varying hydraulic retention times (HRT: 24, 18, 12, 6 and 3 h) on hydrogen production and COD removal in a continuous ABR were operated at room temperature (32.3 ± 1.5 °C). Hydrogen production rate (HPR) increased with a reduction in HRT i.e. from 164.45 ± 4.14 mL H₂/L.d (24 h HRT) to 883.19 ± 7.89 mL H₂/L.d (6 h HRT) then decreased to 748.54 ± 13.84 mL H₂/L.d (3 h HRT). COD removal increased with reduction in HRT i.e. from 14.02 ± 0.58% (24 h HRT) to 29.30 ± 0.84% (6 h HRT) then decreased to 21.97 ± 0.94% (3 h HRT). HRT of 6 h was the optimum condition for ABR operation as indicated.     

Hydrogen production using biocathode single-chamber microbial electrolysis cells fed by molasses wastewater at low temperature

Molasses is by-product from sugar beet process and commonly used as raw material for ethanol production. However, the molasses wastewater possesses high level of chemical oxygen demand (COD), which needs to be properly treated before discharge. In this work, MEC technology, a promising method for hydrogen production from organic waste, was utilized to produce H₂ from molasses wastewater. In this study, the feasibility of operating the MEC at low temperatures was evaluated since the average wastewater temperature in Harbin city is lower than 10 °C. In addition, the feasibility of using biocathode as an alternative to expensive platinum (Pt) as the cathode material was also examined. Both Pt catalyzed MECs and biocathodic MECs were operated at a low temperature of 9 °C. The overall hydrogen recovery of 72.2% (E_ap = 0.6 V) was obtained when the Pt catalyst was used. In contrast, when a cheaper catalyst (biocathode; E_ap = 0.6 V) was used, hydrogen can still be produced but at a lower overall hydrogen recovery of 45.4%. This study demonstrated that hydrogen could be generation from molasses wastewater at a low temperature using a cheaper cathode material (i.e., biocathode).     

An approach of auxiliary carbohydrate source on stabilized biohythane production and energy recovery by two-stage anaerobic process from swine manure

In this study, a two-stage biohythane production system was used to treat swine manure to solve the high Chemical Oxygen Demand (COD) concentration and verify the total energy recovery between the two-stage and a traditional single-stage system. Experiments were carried out in single-stage methane production, two-stage biohythane production in long Hydraulic Retention Time (HRT), and short HRT. The COD removal efficiency and energy recovery were finally compared between single-stage (CH₄ fermenter) and two-stage (H₂+ CH₄ fermenter) systems. The results showed that the methane production rate of 53.2 ± 2.7 mL/d.L, the COD removal efficiency of 29.6 ± 5.8%, and total energy recovery of 2.9 ± 0.1 kJ/L.d was obtained in the single-stage of methane production system with HRT 11.08 d, pH 7, and temperature 55 °C, respectively. In the two-stage of hydrogen and methane productions system, the hydrogen production rate of 1.8 ± 0.7 mL/d.L, the methane production rate of 65.7 ± 2.5 mL/d.L, the COD removal rate was 97.8 ± 1.7%, and the total energy recovery of 3.6 ± 0.1 kJ/L.d was obtained and stabilized when the sugary wastewater content gradually reduced to 0%. This study shows that the methane production rate increases 20%, COD removal efficiency increases to 97.8 ± 1.7%, and total energy recovery increases 30%. At the same time, the single-stage (CH₄ fermenter) switched to a two-stage (H₂+ CH₄ fermenter) system. The two-stage anaerobic biohythane production system successfully treated the high organic swine manure and obtained a higher energy recovery against the traditional single-stage of the biomethane production system.     

Enhancing biohydrogen production from sugar industry wastewater using metal oxide/graphene nanocomposite catalysts in microbial electrolysis cell

Biohydrogen production through Microbial Electrolysis Cell (MEC) has drifted towards the development of suitable cost-effective cathode catalysts. In this study, two graphene hybrid metal oxide nanocomposites were used as catalysts to investigate hydrogen production in the MEC operated with sugar industry wastewater as substrate against phosphate buffer catholyte. Electrochemical characterizations exposed the better performance of NiO.rGO coated cathode which showed lesser overpotential at 600 mV and overall lowest resistance in the Nyquist plots than Ni-foam and Co₃O₄.rGO cathodes. The experimental results showed that at an applied voltage 1.0 V, NiO.rGO nanocomposite had exhibited maximum hydrogen production rate of 4.38 ± 0.11 mmol/L/D, Coloumbic efficiency of 65.6% and Cathodic hydrogen recovery of 20.8% respectively. The MEC performance in terms of biohydrogen production was 1.19 and 2.68 times higher than Co₃O₄.rGO and uncoated Ni-Foam. Hence, economical hybrid nanocomposite catalysts were demonstrated in MEC using industrial effluent for energy and environment sustainability.     

Process engineering for stable power recovery from dairy wastewater using microbial fuel cell

Microbial fuel cells (MFCs) are one of the sustainable technologies that can effectively treat wastewater with concomitant generation of electricity. The present study investigated the treatment of real dairy wastewater (RDW) using Shewanella algae (MTCC-10608) within a single chamber microbial fuel cell (SCMFC). The study was conducted in both batch and fed-batch modes with initial chemical oxygen demand (COD) of 4000 mg/L and 2000 mg/L, respectively, in 0.2 L working volume of RDW for 15 days. However, the fed-batch strategy involved subsequent feeding of dairy wastewater with 6000 mg/L and 8000 mg/L COD on the 5th and 10th day, respectively. This two-step feeding strategy resulted in a maximum open-circuit voltage of 666 mV at 286 h of incubation with a COD removal efficiency of 92.21% and a columbic efficiency of 27.45%. The kinetic studies predicted the saturation constant of 55.83 mg COD/L and current density of 143.3 mA/m², which are similar to the findings from the experiments and polarization curve obtained. The maximum current density and power density from experiments were found to be 141 mA/m² and 50 mW/m² respectively. Thus, this study successfully indicates the utilization of dairy wastewater as a potential substrate for the sustainable power generation using Shewanella algae as a biocatalyst in the microbial fuel cell.     

Co-generation of hydrogen and electricity from biodiesel process effluents

In this study, we apply a short-term voltage (0.2–0.8 V) to both crude glycerol (CG) and an anaerobic digestion (AD) effluent in a single-chamber microbial fuel cell (MFC) for power production. This improves the bioelectrogenesis in both CG (in MFC-1) and the AD effluent (in MFC-2), but higher power generation is attained in MFC-2. The use of domestic and synthetic wastewaters in the AD process leads to the generation of 195 and 350 mL H₂/L-medium, respectively. MFC-2 performs better than MFC-1 in terms of both voltage generation and chemical oxygen demand (COD) reduction. The application of 0.8 V yields a power density of 311 mW/m² (1.94 times higher than that of the control (160 mW/m²)). In addition, MFC-2 exhibits a 70% COD removal at 0.8 V, which decreases to 56% at 0.2 V. Thus, the application of a short-term voltage in MFC can stimulate both bioelectrogenesis and COD removal.     

Hydrogen gas production from vinegar fermentation wastewater by electro-hydrolysis: Effects of initial COD content

Vinegar fermentation wastewater with different initial COD contents (9.66–48.6 g L⁻¹) were used for hydrogen gas production with simultaneous COD removal by electro-hydrolysis. The applied DC voltage was constant at 4 V. The highest cumulative hydrogen production (3197 ml), hydrogen yield (2766 ml H₂ g⁻¹ COD), hydrogen formation rate (799 ml d⁻¹), and percent hydrogen (99.5%) in the gas phase were obtained with the highest initial COD of 48.6 g COD L⁻¹. The highest energy efficiency (48%) was obtained with the lowest COD content of 9.66 g L⁻¹. Hydrogen gas production by water electrolysis was less than 250 ml and wastewater control resulted in less than 25 ml H₂ in 96 h. The highest (12%) percent COD removal was obtained with the lowest COD content. Hydrogen gas was produced by reaction of (H⁺) ions present in raw WW ( pH = 3.0) and protons released from acetic acid with electrons provided by electrical current. Electro-hydrolysis of vinegar wastewater was proven to be an effective method of H₂ gas production with some COD removal.     

Treatment of dairy wastewater using anaerobic and solar photocatalytic methods

The present study was aimed to treat the dairy wastewater by using anaerobic and solar photocatalytic oxidation methods. The anaerobic treatment was carried out in a laboratory scale hybrid upflow anaerobic sludge blanket reactor (HUASB) with a working volume of 5.9 L. It was operated at organic loading rate (OLR) varying from 8 to 20 kg COD/m³ day for a period of 110 days. The maximum loading rate of the anaerobic reactor was found to be 19.2 kg COD/m³ day and the corresponding chemical oxygen demand (COD) removal at this OLR was 84%. The anaerobically treated wastewater at an OLR of 19.2 kg COD/m³ day was subjected to secondary solar photocatalytic oxidation treatment. The optimum pH and catalyst loading for the solar photochemical oxidation was found to be 5 and 300 mg/L, respectively. The secondary solar photocatalytic oxidation using TiO₂ removed 62% of the COD from primary anaerobic treatment. Integration of anaerobic and solar photocatalytic treatment resulted in 95% removal of COD from the dairy wastewater. The findings suggest that anaerobic treatment followed by solar photo catalytic oxidation would be a promising alternative for the treatment of dairy wastewater.     

Optimizing energy harvest in wastewater treatment by combining anaerobic hydrogen producing biofermentor (HPB) and microbial fuel cell (MFC)

This study focused on the optimization of energy harvest from wastewater treatment by integrating two novel biotechnologies: anaerobic hydrogen production and microbial fuel cell (MFC). The simultaneous production of hydrogen and electricity from wastewater was examined at continuous flow at different organic loading rates (OLR) by changing chemical oxygen demand (COD) and hydraulic retention time (HRT). The experimental results showed that the specific hydrogen yield (SHY, mole H₂/mole glucose) increased with the decrease in OLR, and reached at the maximum value of 2.72 mol H₂/mole glucose at the lowest OLR of 4 g/L.d. The effluent from hydrogen producing biofermentor (HPB) was fed to a single chamber MFC (SCMFC), obtaining the highest power density and coulombic efficiency (CE) of 4200 mW/m³ and 5.3%, respectively. The energy conversion efficiency (ECE) increased with OLR and reached the peak value of 4.24% at the OLR of 2.35 g/L.d, but decreased with higher OLR. It was demonstrated that the combination of HPB and MFC improved the ECE and COD removal with the maximum total ECE of 29% and COD removal of 71%. The kinetic analysis was conducted for the HPB-MFC hybrid system. The maximum hydrogen production was projected to be 2.85 mol H₂/mole glucose. The maximum energy recovery and COD removal efficiency from MFC were projected to be 559 J/L and 97%, respectively.     

Hydrogen and methane production in a bio-electrochemical system assisted anaerobic baffled reactor

In this study, a new process was proposed to enhance the stability and efficiency of an anaerobic baffled reactor (ABR). The process was examined in a four equal compartments ABR with total volume of 3.46 L. The first compartment was operated for fermentative hydrogen production and the last three compartments were used as continuous singer chamber microbial electrolysis cells (MECs) for methanogenesis. The system was operated at 35 ± 1 °C and hydraulic retention time (HRT) of 24 h with influent chemical oxygen demand (COD) concentration of 3500 mg/L–4000 mg/L. The results indicated that the proportion of hydrogen in the first compartment was 20.7% and proportions of methane in the last three compartments were 98.0%, 93.6% and 70.1%, respectively. A total of 98.0% of COD removal rate was achieved as well. Hence, this new system has following advantages: hydrogen production with cleaner effluent, high COD removal rate, and net methane production for practical use.     

Dark fermentative biohydrogen production from confectionery wastewater in continuous-flow reactors

The production of biohydrogen from industrial wastewater through the dark fermentation (DF) process has attracted increased interest in recent years. To implement a DF process on a large scale, a thorough knowledge of laboratory scale process control is required. The operating parameters and design features of the reactors have a great influence on the efficiency of the process. In this work, the possibility of continuous production of biohydrogen from confectionery wastewater was evaluated. The DF process was carried out at 37 ± 1 °C in two different reactors: an upflow anaerobic filter (AF) and a fluidized bed reactor (AFB). Polyurethane foam (PU) was used to immobilize the biomass. The DF process was studied at four hydraulic retention times (HRT) (1.5, 2.5, 7.5 and 15 days) and the corresponding organic loading rates (OLR) (9.21, 6.12, 2.04 and 1.02 g COD_init/(L day)). The highest hydrogen yield (HY) (44.73 ml/g COD_init) and hydrogen production rate (HPR) (92.5 ml/(L day)) was observed in AFB at HRT of 7.5 days and 2.5 days, respectively. The highest concentration of hydrogen in biogas was 34% in AF and 36% in AFB at HRT of 7.5 days. In contrast to AF, the COD removal efficiency in AFB increased with increasing HRT. The pH of the effluent was low (3.95–4.38). However, due to the use of PU for biomass immobilization, it is possible that there were local zones in the reactor that were optimal for the functioning of not only acidogens, but also methanogens. This was evidenced by a rather high content of methane in biogas (2.5% in AF and 9.6% in AFB at HRT of 15 days). These results provide valuable data for optimizing the continuous DF of wastewater from confectionery and other food industries to produce biohydrogen or biohythane.     

Powering microbial electrolysis cells by electricity generation from simulated waste heat of anaerobic digesters using thermoelectric generators

Waste heat from anaerobic digesters can be converted to electricity by using thermoelectric generators (TEG). Herein, such energy was employed to power a microbial electrolysis cell (MEC) for producing hydrogen gas. Four TEG units could deliver a voltage of ~0.5 V, sufficient to drive the MEC that achieved a hydrogen production rate of 0.48 ± 0.13 m³ m⁻³ d⁻¹. This rate was further improved to 0.75 ± 0.05 m³ m⁻³ d⁻¹ when the temperature difference for TEG was increased from 18 to 28 °C. There was no significant difference between the TEG-powered MEC and power supply-supported MEC (at 0.6 V), in terms of current generation, hydrogen production, and organic removal. Ambient air was also studied as a cold-side source for TEG, although some challenges were encountered to maintain a large temperature difference. Those results will encourage further exploration of using TEG as a feasible power supply for sustainable MEC operation.     

Hydrogen production from alcohol wastewater with added fermentation residue by an anaerobic sequencing batch reactor (ASBR) under thermophilic operation

The objective of this study was to investigate the enhancement of hydrogen production from alcohol wastewater by adding fermentation residue using an anaerobic sequencing batch reactor (ASBR) under thermophillic operation (55 °C) and at a constant pH of 5.5. The digestibility of the added fermentation residue was also evaluated. For a first set of previous experiments, the ASBR system was operated to obtain an optimum COD loading rate of 50.6 kg/m³ d of alcohol wastewater without added fermentation residue and the produced gas contained 31% H₂ and 69% CO₂. In this experiment, the effect of added fermentation residue (100–1200 mg/l) on hydrogen production performance was investigated under a COD loading rate of 50.6 kg/m³ d of the alcohol wastewater. At a fermentation residue concentration of 1000 mg/l, the produced gas contained 40% H₂ and 60% CO₂ without methane and the system gave the highest hydrogen yield and specific hydrogen production rate of 128 ml/g COD removed and 2880 ml/l d, respectively. Under thermophilic operation with a high total COD loading rate (51.8 kg/m³ d) and a short HRT (21 h) at pH 5.5, the ASBR system could only break down cellulose (41.6%) and hemicellulose (21.8%), not decompose lignin.     

Biohydrogen production from soluble condensed molasses fermentation using anaerobic fermentation

Using anaerobic micro-organisms to convert organic waste to produce hydrogen gas gives the benefits of energy recovery and environmental protection. The objective of this study was to develop a biohydrogen production technology from food wastewater focusing on hydrogen production efficiency and micro-flora community at different hydraulic retention times. Soluble condensed molasses fermentation (CMS) was used as the substrate because it is sacchariferous and ideal for hydrogen production. CMS contains nutrient components that are necessary for bacterial growth: microbial protein, amino acids, organic acids, vitamins and coenzymes. The seed sludge was obtained from the waste activated sludge from a municipal sewage treatment plant in Central Taiwan. This seed sludge was rich in Clostridium sp.A CSTR (continuously stirred tank reactor) lab-scale hydrogen fermentor (working volume, 4.0 L) was operated at a hydraulic retention time (HRT) of 3–24 h with an influent CMS concentration of 40 g COD/L. The results showed that the peak hydrogen production rate of 390 mmol H₂/L-d occurred at an organic loading rate (OLR) of 320 g COD/L-d at a HRT of 3 h. The peak hydrogen yield was obtained at an OLR of 80 g COD/L-d at a HRT of 12 h. At HRT 8 h, all hydrogenase mRNA detected were from Clostridium acetobutylicum-like and Clostridium pasteurianum-like hydrogen-producing bacteria by RT-PCR analysis. RNA based hydrogenase gene and 16S rRNA gene analysis suggests that Clostridium exists in the fermentative hydrogen-producing system and might be the dominant hydrogen-producing bacteria at tested HRTs (except 3 h). The hydrogen production feedstock from CMS is lower than that of sucrose and starch because CMS is a waste and has zero cost, requiring no added nutrients. Therefore, producing hydrogen from food wastewater is a more commercially feasible bioprocess.