Electrohydrolysis of landfill leachate organics for hydrogen gas production and COD removal

Hydrogen gas production with simultaneous COD removal was realized by application of DC voltages (0.5-5.0 V) to landfill leachate. The rate and the yield of hydrogen gas production were investigated at different DC voltages by using aluminum electrodes and DC power supply. The highest cumulative hydrogen production (5000 mL), hydrogen yield (2400 mL H₂ g⁻¹ COD), daily hydrogen gas formation (1277 mL d⁻¹), and percent hydrogen (99%) in the gas phase were obtained with 4 V DC voltage. Energy conversion efficiency (H₂ energy/electrical energy) reached the highest level (80.6%) with 1 V DC voltage. Hydrogen gas production was mainly realized by electrohydrolysis of leachate organics due to negligible H₂ gas production in water and leachate control experiments. The highest COD removal (77%) was also obtained with 4 V DC voltage. Electrohydrolysis of landfill leachate was proven to be an effective method for hydrogen gas production with simultaneous COD removal.     

Hydrogen gas production from olive mill wastewater by electrohydrolysis with simultaneous COD removal

Diluted olive mill wastewater (OMW) was subjected to direct current (DC) voltages (0.5-4.0 V) for hydrogen gas production with simultaneous chemical oxygen demand (COD) removal by electrohydrolysis. The highest cumulative hydrogen production (3020 ml) and hydrogen yield (2500 ml H₂ g⁻¹ COD) were obtained with 3 V DC voltage while the highest current intensity (80 mA), percent hydrogen (95%) in the gas phase, hydrogen gas formation rate (614 ml d⁻¹), percent COD removal (44%) and energy conversion efficiency (95%) were realized with 2 V. Hydrogen gas production by electrolysis of water was negligible for all voltages. COD removal from OMW with no DC voltage application was usually lower than that obtained with DC power application. Hydrogen gas production by electrohydrolysis of OMW was proven to be a fast and effective method with simultaneous COD removal.     

Hydrogen gas production from waste anaerobic sludge by electrohydrolysis: Effects of applied DC voltage

Waste anaerobic sludge was subjected to different DC voltages (0.5-5 V) for hydrogen gas production by using aluminum electrodes and a DC power supply. Effects of applied DC voltage on the rate and extent of hydrogen gas production were investigated. The highest cumulative hydrogen production (2775 ml), daily hydrogen gas formation (686.7 ml d⁻¹), hydrogen yield (96 ml H₂ g⁻¹ COD) and percent hydrogen (94.3%) in the gas phase were obtained with 2 V DC voltage. Energy conversion efficiency (H₂ energy/electrical energy) also reached the highest level (74%) with 2 V DC voltage application. Control experiments with no voltage application to the sludge yielded almost the same level of COD removal, but no hydrogen gas production. Voltage application to water resulted in much lower hydrogen gas production as compared to sludge indicating negligible electrolysis of water. The results indicated that the sludge was naturally decomposed by the active cells removing COD and releasing hydrogen ions to the medium which reacted with the electrons provided by DC current to produce hydrogen gas. Hydrogen gas production from electrohydrolysis of waste sludge was found to be a fast and effective method with high energy efficiency.     

Improved hydrogen gas production in electrohydrolysis of vinegar fermentation wastewater by scrap aluminum and salt addition

Scrap aluminum particles and salt (NaCl) were added to the vinegar fermentation wastewater to improve hydrogen gas formation by electrohydrolysis of the wastewater organics. The applied DC voltage and initial COD of the wastewater were constant at 4 V and 33.16 g L⁻¹, respectively. The highest cumulative hydrogen gas formation (2877 mL) was obtained with scrap Al (1 g L⁻¹) and NaCl (1 g L⁻¹) additions within 72 h as compared to 1925 mL H₂ gas formation from raw wastewater. Hydrogen gas formation from Al and NaCl added water was 302 ml as compared to 260 ml from raw water. The highest H₂ gas formation rate (952 mL d⁻¹), the yield (1660 mL H₂ g⁻¹ COD) and the highest current intensity (163 mA) were also obtained with combined effects of scrap Al and NaCl additions. Almost pure hydrogen gas (99%) was produced using the raw wastewater. Initial conductivity of the raw wastewater increased from 1.80 mS cm⁻¹ to 5.01 mS cm⁻¹ with the addition of scrap Al and salt for which the final conductivities were 4.0 mS cm⁻¹ and 6.91 mS cm⁻¹, respectively. The highest energy conversion efficiency was obtained with only scrap Al addition (37.8%) as compared to 30.5% efficiency obtained with Al and salt additions. Additions of NaCl and scrap Al particles was found to be very beneficial for H₂ gas formation by electrohydrolysis of vinegar fermentation wastewater.     

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.     

Electro-hydrolysis of cheese whey solution for hydrogen gas production and chemical oxygen demand (COD) removal using photo-voltaic cells (PVC)

Diluted cheese whey (CW) solution was used for hydrogen gas production by electro-hydrolysis using photo-voltaic cells (PVC) as source of electricity. Effects of initial chemical oxygen demand (COD) concentration on the rate and yield of hydrogen gas production were investigated using a completely mixed and sealed reactor with aluminum electrodes. Cumulative hydrogen gas formation (CHF) increased with increasing initial COD concentration. The highest cumulative hydrogen gas volume (26472 mL), hydrogen gas production rate (4553 mL d⁻¹), hydrogen yield (7004 mL H₂ g⁻¹ COD), and percent COD removal (21.5%) were obtained with initial COD of 35172 mg L⁻¹. H₂ gas formation from water control was only 5365 mL. pH of the CW solution increased with decreasing conductivities during the course of experiments. Gas phase contained more than 99% H₂ at the end of experiments. The highest energy efficiency (20.4%) was also obtained with the highest COD content. Nearly pure hydrogen gas formation by electro-hydrolysis of cheese whey using PVC panels was proven to be an effective method.     

Hydrogen gas production from food wastes by electrohydrolysis using a statical design approach

Hydrogen gas production was investigated by electrohydrolysis of food waste due to its high organic content. Different voltages generated by DC power supply were applied to food waste in order to produce hydrogen gas. Effects of the DC voltage, reaction time and initial solid content on cumulative hydrogen gas production, hydrogen gas content in the gas phase and total organic carbon (TOC) removal were investigated by using a Box-Behnken statistical experiment design approach. The most suitable voltage/reaction time/solid content values resulting in the highest hydrogen gas content (99%), the highest cumulative hydrogen gas formation (7000 mL) and total organic carbon removal (33%) were determined as 5 V/75 h/20%. The results indicated that food wastes constitute a good source for H₂ gas production by electrohydrolysis. Hydrogen gas produced by electrohydrolysis of food waste can be directly used in fuel cells due to its high putrity.     

Effects of metals in wastewater on hydrogen gas production using electrohydrolysis

Hydrogen gas was produced from metal plating wastewater by electro hydrolysis. Wastewater contains chrome, copper and nickel metals which can accelerate the production of hydrogen gas. Effects of kind of metals, the voltage and reaction time on percent hydrogen gas (HGP) were investigated. After application of different DC voltages on each metallic wastewater, percent hydrogen gas (HGP), cumulative hydrogen gas volume (CHGV), hydrogen gas formation rate (HFR) and total organic carbon (TOC) removal were also evaluated. Hydrogen gas percent was obtained as %99 at 4 V for chrome plating wastewater while percent hydrogen gas was achieved as 50% H₂ gas at 4 V for copper and nickel metal plating wastewater. Maximum CHGV achieved with 4 V DC voltage for all metal plating wastewater. Maximum CHGV (4000 mL), HFR (985 mL H₂ d⁻¹) and percent hydrogen gas (99%) was observed with chrome plating wastewater at 4 V DC voltage. Hydrogen gas produced from chrome metal plating wastewater using electro hydrolysis method can be efficiently used for fuel cells as a source due to nearly pure hydrogen gas.     

Hydrogen gas production by electrohydrolysis of volatile fatty acid (VFA) containing dark fermentation effluent

Dark fermentation effluents of wheat powder (WP) solution containing different concentrations of volatile fatty acids (VFAs) were subjected to low voltage (1–3 V) DC current to produce hydrogen gas. Graphite and copper electrodes were tested and the copper electrode was found to be more effective due to higher electrical conductivity. The effects of solution pH (2–7), applied voltage (1–3 V) and the total VFA (TVFA) concentration (1–5 g L⁻¹) on hydrogen gas production were investigated. Hydrogen production increased with decreasing pH and became maximum at pH = 2. Increases in applied voltage and the TVFA concentration also increased the cumulative hydrogen formation. The most suitable conditions for the highest cumulative hydrogen production was pH = 2, with 3 V applied voltage and 5 g TVFA L⁻¹. Up to 110 ml hydrogen gas was obtained with 5 g L⁻¹ TVFA at pH = 5.8 and 2 V applied voltage within 37.5 h. The highest energy efficiency (56%) was obtained with the 2 V applied voltage and 10.85 g L⁻¹ TVFA. Hydrogen production by electrolysis of water in control experiments was negligible for pH > 4. Hydrogen production by electrohydrolysis of VFA containing anaerobic treatment effluents was found to be an effective method with high energy efficiency.     

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.     

Photo-fermentative hydrogen gas production from dark fermentation effluent of acid hydrolyzed wheat starch with periodic feeding

Hydrogen gas production by photo-fermentation of dark fermentation effluent of acid hydrolyzed wheat starch was investigated at different hydraulic residence times (HRT = 1-10 days). Pure Rhodobacter sphaeroides (NRRL B-1727) culture was used in continuous photo-fermentation by periodic feeding and effluent removal. The highest daily hydrogen gas production (85 ml d⁻¹) was obtained at HRT = 4 days (96 h) while the highest hydrogen yield (1200 ml H₂ g⁻¹ TVFA) was realized at HRT = 196 h. Specific and volumetric hydrogen formation rates were also the highest at HRT = 96 h. Steady-state biomass concentrations and biomass yields increased with increasing HRT. TVFA loading rates of 0.32 g L⁻¹ d⁻¹ and 0.51 g L⁻¹ d⁻¹ resulted in the highest hydrogen yield and formation rate, respectively. Hydrogen gas yield obtained in this study compares favorably with the relevant literature reports probably due to operation by periodic feeding and effluent removal.     

Comparison of microbial electrolysis cells operated with added voltage or by setting the anode potential

Hydrogen production in a microbial electrolysis cell (MEC) can be achieved by either setting the anode potential with a potentiostat, or by adding voltage to the circuit with a power source. In batch tests the largest total gas production (46 ± 3 mL), lowest energy input (2.3 ± 0.3 kWh/m³ of H₂ generated), and best overall energy recovery (?_E+S = 58 ± 6%) was achieved at a set anode potential of E_An = −0.2 V (vs Ag/AgCl), compared to set potentials of −0.4 V, 0 V and 0.2 V, or an added voltage of E_ap = 0.6 V. Gas production was 1.4 times higher with E_An = −0.2 V than with E_ap = 0.6 V. Methane production was also reduced at set anode potentials of −0.2 V and higher than the other operating conditions. Continuous flow operation of the MECs at the optimum condition of E_An = −0.2 V initially maintained stable hydrogen gas production, with 68% H₂ and 21% CH₄, but after 39 days the gas composition shifted to 55% H₂ and 34% CH₄. Methane production was not primarily anode-associated, as methane was reduced to low levels by placing the anode into a new MEC housing. These results suggest that MEC performance can be optimized in terms of hydrogen production rates and gas composition by setting an anode potential of −0.2 V, but that methanogen proliferation must be better controlled on non-anodic surfaces.     

Sulfate-reducing bacteria as new microorganisms for biological hydrogen production

Sulfate-reducing bacteria (SRB) have an extremely high hydrogenase activity and in natural habitats where sulfate is limited, produce hydrogen fermentatively. However, the production of hydrogen by these microorganisms has been poorly explored. In this study we investigated the potential of SRB for H₂ production using the model organism Desulfovibrio vulgaris Hildenborough. Among the three substrates tested (lactate, formate and ethanol), the highest H₂ production was observed from formate, with 320 mL L⁻¹_medium of H₂ being produced, while 21 and 5 mL L⁻¹_medium were produced from lactate and ethanol, respectively. By optimizing reaction conditions such as initial pH, metal cofactors, substrate concentration and cell load, a production of 560 mL L⁻¹_medium of H₂ was obtained in an anaerobic stirred tank reactor (ASTR). In addition, a high specific hydrogen production rate (4.2 L g⁻¹_dcw d⁻¹; 7 mmol g⁻¹_dcw h⁻¹) and 100% efficiency of substrate conversion were achieved. These results demonstrate for the first time the potential of sulfate reducing bacteria for H₂ production from formate.     

Hydrogen gas production from cheese whey powder (CWP) solution by thermophilic dark fermentation

Hydrogen gas production from cheese whey powder (CWP) solution by thermophilic dark fermentation was investigated at 55 °C. Experiments were performed at different initial total sugar concentrations varying between 5.2 and 28.5 g L⁻¹ with a constant initial bacteria concentration of 1 g L⁻¹. The highest cumulative hydrogen evolution (257 mL) was obtained with 20 g L⁻¹ total sugar (substrate) concentration within 360 h while the highest H₂ formation rate (2.55 mL h⁻¹) and yield (1.03 mol H₂ mol⁻¹ glucose) were obtained at 5.2 and 9.5 g L⁻¹ substrate concentrations, respectively. The specific H₂ production rate (SHPR = 4.5 mL h⁻¹ g⁻¹cells) reached the highest level at 20 g L⁻¹ total sugar concentration. Total volatile fatty acid (TVFA) concentration increased with increasing initial total sugar content and reached the highest level (14.15 g L⁻¹) at 28.5 g L⁻¹ initial substrate concentration. The experimental data was correlated with the Gompertz equation and the constants were determined. The optimum initial total sugar concentration was 20 g L⁻¹ above which substrate and product (VFA) inhibitions were observed.     

TiO2 nanotubes for hydrogen generation by photocatalytic water splitting in a two-compartment photoelectrochemical cell

Highly ordered TiO₂ nanotube arrays for hydrogen production have been synthesized by electrochemical anodization of titanium sheets. Under solar light irradiation, hydrogen generation by photocatalytic water splitting was carried out in the two-compartment photoelectrochemical cell without any external applied voltage. The hydrogen gas and oxygen generated on Pt side and on TiO₂ nanotubes side respectively were efficiently separated. The effect of anodization time on the morphology structures, photoelectrochemical properties and hydrogen production was systematically investigated. Due to more charge carrier generation and faster charge transfer, a maximum photoconversion efficiency of 4.13% and highest hydrogen production rate of 97 μmol h⁻¹cm⁻² (2.32 mL h⁻¹cm⁻²) were obtained from TiO₂ nanotubes anodized for 60 min.     

Mesophilic fermentative hydrogen production from sago starch-processing wastewater using enriched mixed cultures

Biohydrogen (bioH₂) production from starch-containing wastewater is an energy intensive process as it involves thermophilic temperatures for hydrolysis prior to dark fermentation. Here we report a low energy consumption bioH₂ production process with sago starch powder and wastewater at 30 °C using enriched anaerobic mixed cultures. The effect of various inoculum pretreatment methods like heat (80 °C, 2 h), acid (pH 4, 2.5 N HCl, 24 h) and chemical (0.2 g L⁻¹ bromoethanesulphonic acid, 24 h) on bioH₂ production from starch powder (1% w/v) showed highest yield (323.4 mL g⁻¹ starch) in heat-treatment and peak production rate (144.5 mL L⁻¹ h⁻¹) in acid-treatment. Acetate (1.07 g L⁻¹) and butyrate (1.21 g L⁻¹) were major soluble metabolites of heat-treatment. Heat-treated inoculum was used to develop mixed cultures on sago starch (1% w/v) in minimal medium with 0.1% peptone-yeast extract (PY) at initial pH 7 and 30 °C. The effect of sago starch concentration, pH, inoculum size and nutrients (PY and Fe ions) on batch bioH₂ production showed 0.5% substrate, pH 7, 10% inoculum size and 0.1% PY as the best H₂ yielding conditions. Peak H₂ yield and production rate were 412.6 mL g⁻¹ starch and 78.6 mL L⁻¹ h⁻¹, respectively at the optimal conditions. Batch experiment results using sago-processing wastewater under similar conditions showed bioH₂ yield of 126.5 mL g⁻¹ COD and 456 mL g⁻¹ starch. The net energy was calculated to be +2.97 kJ g⁻¹ COD and +0.57 kJ g⁻¹ COD for sago starch powder and wastewater, respectively. Finally, the estimated net energy value of +2.85 × 10¹³ kJ from worldwide sago-processing wastewater production indicates that this wastewater can serve as a promising feedstock for bioH₂ production with low energy input.     

Hydrogen and methane production via a two-stage processes (H2-SBR + CH4-UASB) using tequila vinasses

The feasibility of producing hydrogen and methane via a two-stage fermentation of tequila vinasses was evaluated in sequencing batch (SBR) and up-flow anaerobic sludge blanket (UASB) reactors. Different vinasses concentrations ranging from 500 mg COD/L to 16 g COD/L were studied in SBR by using thermally pre-treated anaerobic sludge as inoculum for hydrogen production. Peak volumetric hydrogen production rate and specific hydrogen production were attained as 57.4 ± 4.0 mL H₂/L-h and 918 ± 63 mL H₂/gVSS-d, at the substrate concentration of 16 g COD/L and 6 h of hydraulic retention time (HRT). Increasing substrate concentration has no effect on the specific hydrogen production rate. The fermentation effluent was used for methane production in an UASB reactor. The higher methane composition in the biogas was achieved as 68% at an influent concentration of 1636 mg COD/L. Peak methane volumetric, specific production rates and yield were attained as 11.7 ± 0.7 mL CH₄/L-h, 7.2 ± 0.4 mL CH₄/g COD-h and 257.9 ± 13.8 mL CH₄/g COD at 24 h-HRT and a substrate concentration of 1636 mg COD/L. An overall organic matter removal (SBR + UASB) in this two-stage process of 73–75% was achieved.     

Application of an electric field for pretreatment of a feedstock (Laminaria japonica) for dark fermentative hydrogen production

When using cellulosic biomass as feedstock for dark fermentative hydrogen production (DFHP), feedstock preparation is essential step for enhancement of biodegradability. In the present work, electric field was newly applied as a novel pretreatment technique to Laminaria japonica, a marine brown algae, as an alternative method for feedstock preparation. A feasibility test was first conducted (20–100 V for 30 min). The highest H₂ yield (93.6 mL H₂ g⁻¹ dry cell weight (dcw)) was achieved at applied voltage of 60 V, while the performance was decreased from applied voltage of 80–100 V due to increasing formation of hydroxymethylfurfural. Subsequently, electric pretreatment conditions (applied voltage and reaction time) were statistically optimized, and a H₂ yield of 102.7 mL g⁻¹ dcw was recorded with applied voltage 58.5 V and reaction time 30 min. This was 96.1% of the predicted value. These findings clearly revealed that the application of electric field as pretreatment method has enormous potential as an alternative method for feedstock preparation in DFHP.     

Hydrogen sensing characteristics of a Pd/Nickel oxide/GaN-based Schottky diode

Hydrogen sensing characteristics of a novel metal-oxide-semiconductor (MOS) Schottky diode are thoroughly investigated. The MOS structure consists of a gallium nitride (GaN)-based semiconductor system, a nickel oxide (NiO) layer, and palladium (Pd) catalytic materials. A well-prepared Pd/NiO/GaN-based diode shows several advantages in relation to hydrogen sensing, including a simple structure, high sensing speed, wide flexibility for operation under both forward and reverse applied voltages, and a good sensing response of 8.1 × 10³ under an applied forward voltage of 0.25 V, at 300 K in a 1% H₂/air ambience. Furthermore, under an applied reverse voltage of −2 V and at a high temperature of 573 K, this MOS diode shows a response as high as 1.8 × 10⁴ towards 1% H₂/air mixture gas. The Schottky diode sensor with a novel Pd/NiO/GaN structure demonstrated in this study is a promising candidate for high-performance hydrogen sensing applications.     

Hydrogen production and ammonium recovery from urine by a Microbial Electrolysis Cell

We investigated the use of a Microbial Electrolysis Cell (MEC) for the ammonium removal, COD removal and hydrogen production from five times diluted urine. During operation with a batch cathode, a current density of 23.07 ± 1.15 A m⁻² was achieved corresponding to a hydrogen production rate of 48.6 ± 7.47 m³ H₂ m⁻³ MEC d⁻¹, an ammonium removal rate of 173.4 ± 18.1 g N m⁻² d⁻¹ and a COD removal rate of 171.0 ± 16.9 g COD m⁻² d⁻¹. Ammonia stripping was not possible in the applied MEC and ammonia diffusion from cathode to anode compartment led to a relatively short stable operation period. The stable operation period was prolonged by addition of new cathode media (HRT 6 h), but this resulted in a lower current density (14.64 ± 1.65 A m⁻²), hydrogen production rate (32.0 ± 0.89 m³ H₂ m⁻³ MEC d⁻¹), ammonium removal rate (162.18 ± 10.37 g N m⁻² d⁻¹) and COD removal rate (130.56 ± 4.45 g COD m⁻² d⁻¹).