Production & Supply Chain

Hydrogen is the most efficient energy carrier. Hydrogen can be obtained from different sources of raw materials including water. Among many hydrogen production methods eco-friendly and high purity of hydrogen can be obtained by water electrolysis. However In terms of sustainability and environmental impact PEM water electrolysis was considered as most promising techniques for high pure efficient hydrogen production from renewable energy sources and emits only oxygen as byproduct without any carbon emissions. Moreover the produced hydrogen (H₂) and oxygen (O₂) directly used for fuel cell and industrial applications. However overall water splitting resulting in only 4% of global industrial hydrogen being produced by electrolysis of water mainly due to the economic issues. Nowadays increased the desire production of green hydrogen has increased the interest on PEM water electrolysis. Thus the considerable research has been completed recently in the development of cost effective electrocatalysts for PEM water electrolysis. In this present review we discussed about the recent developments in the PEM water electrolysis including high performance low cost HER and OER electrocatalysts and their challenges new and old related to electrocatalysts and PEM cell components also addressed. This review will contribute further research improvements and a road map in order to support in developing the PEM water electrolyser as a commercially feasible hydrogen production purpose.

Pressure is mounting on the natural gas and LNG community to reduce methane emissions and this is most urgent in EU countries following the adoption of much tougher greenhouse gas reduction targets of 2030 and the publication of the European Commission’s Methane Strategy. With rapidly declining indigenous EU production and therefore rising import dependence there are increasing calls for emissions from imported pipeline gas and LNG to be quantified and based on actual measurements as opposed to standard emission factors. The Methane Strategy promises to be a significant milestone in that process. Companies which are supplying (or intending to supply) natural gas to the EU – the largest global import market for pipeline gas and a very significant market for LNG – would be well advised to pay close attention to how the regulation of methane emissions is unfolding and to make an immediate and positive response. Failure to do so could accelerate the demise of natural gas in European energy balances faster than would otherwise have been the case and shorten the time available for transition to decarbonised gases – specifically hydrogen – using existing natural gas infrastructure.<br/>This EU initiative will (and arguably already has) attracted attention from non-EU governments and companies involved in global gas and LNG trade. We have already seen deliveries of `carbon neutral’ LNG cargos to Asia as well as a long-term LNG contract in which the greenhouse gas content of cargos will be measured reported and verified (MRV) according to an agreed methodology. Natural gas and LNG exports if based on these standards or those set out in the EU Methane Strategy may be able to command premium prices from buyers eager to demonstrate their own GHG reduction credentials to governments customers and civil society.

Two electrolysis technologies fed with renewable energy sources are promising for the production of CO₂-free hydrogen and enabling the transition to a hydrogen society: Alkaline Electrolyte (AE) and Polymer Electrolyte Membrane (PEM). However limited information exists on the potential environmental impacts of these promising sustainable innovations when operating on a large-scale. To fill this gap the performance of AE and PEM systems is compared using ex-ante Life Cycle Assessment (LCA) technology analysis and exploratory scenarios for which a refined methodology has been developed to study the effects of implementing large-scale sustainable hydrogen production systems. Ex-ante LCA allows modelling the environmental impacts of hydrogen production exploratory scenario analysis allows modelling possible upscaling effects at potential future states of hydrogen production and use in vehicles in the Netherlands in 2050. A bridging tool for mapping the technological field has been created enabling the combination of quantitative LCAs with qualitative scenarios. This tool also enables diversity for exploring multiple sets of visions. The main results from the paper show with an exception for the “ozone depletion” impact category (1) that large-scale AE and PEM systems have similar environmental impacts with variations lower than 7% in all impact categories (2) that the contribution of the electrolyser is limited to 10% of all impact categories results and (3) that the origin of the electricity is the largest contributor to the environmental impact contributing to more than 90% in all impact categories even when renewable energy sources are used. It is concluded that the methodology was applied successfully and provides a solid basis for an ex-ante assessment framework that can be applied to emerging technological systems.

A vision of hydrogen based economy and clean sustainable fossil fuels-free world inspires the scientific community to put much effort into the development of visible-light-driven photochemistry and efficient solar energy harvesting. The unique features of plasmonic nanomaterials such as capability of significant electric field amplification an extreme local heating generation of high energy charge carriers and broad tunability of optical properties coupled to catalytically active surfaces provide an exciting opportunity for hydrogen production with solar photochemistry. This review sums up recent progress in the development of plasmonic thermophotocatalysis paying particular attention to sustainable production of hydrogen. We approach the subject from a broad bottom-up perspective beginning with the brief description of plasmon-related phenomena and plasmon-assisted photochemistry through the demonstration of various plasmonic nanostructures their synthesis and hydrogen production efficiency ending with the idea of continuous-flow reactors and their future implementation in hydrogen production by plasmonic thermophotocatalysis. Finally we summarize the review and highlight the remaining challenges that have to be faced before the widespread commercialization of this technology.

Palladium (Pd) membranes are a promising enabling technology for power generation and hydrogen production with CO2 capture. SINTEF has developed and patented a flexible technology to produce Pd-alloy membranes that significantly improves flux and thereby reduces material costs. Reinertsen AS and SINTEF aim to demonstrate the Pd membrane technology for H2 separation on a side stream of the Statoil Methanol Plant at Tjeldbergodden Norway. In the present article we present the upscaling of the membrane manufacturing process together with the membrane module and skid design and construction.

Interest in blue hydrogen production technologies is growing. Some researchers have evaluated the environmental and/or economic feasibility of producing blue hydrogen but a holistic assessment is still needed. Many aspects of hydrogen production have not been investigated. There is very limited information in the literature on the impact of plant size on production and the extent of carbon capture on the cost and life cycle greenhouse gas (GHG) emissions of blue hydrogen production through various production pathways. Detailed uncertainty and sensitivity analyses have not been included in most of the earlier studies. This study conducts a holistic comparative cost and life cycle GHG emissions’ footprint assessment of three natural gas-based blue hydrogen production technologies – steam methane reforming (SMR) autothermal reforming (ATR) and natural gas decomposition (NGD) to address these research gaps. A hydrogen production plant capacity of 607 tonnes per day was considered. For SMR based on the percentage of carbon capture and capture points we considered two scenarios SMR-52% (indicates 52% carbon capture) and SMR-85% (indicates 85% carbon capture). A scale factor was developed for each technology to understand the hydrogen production cost with a change in production plant size. Hydrogen cost is 1.22 1.23 2.12 1.69 2.36 1.66 and 2.55 $/kg H2 for SMR ATR NGD SMR-52% SMR-85% ATR with carbon capture and sequestration (ATR-CCS) and NGD with carbon capture and sequestration (NGD-CCS) respectively. The results indicate that when uncertainty is considered SMR-52% and ATR are economically preferable to NGD and SMR-85%. SMR-52% could outperform ATR-CCS when the natural gas price decreases and the rate of return increases. SMR-85% is the least attractive pathway; however it could outperform NGD economically when CO2 transportation cost and natural gas price decrease. Hydrogen storage cost significantly impacts the hydrogen production cost. SMR-52% SMR-85% ATR-CCS and NGD-CCS have scale factors of 0.67 0.68 0.54 and 0.65 respectively. The hydrogen cost variation with capacity shows that operating SMR-52% and ATR-CCS above hydrogen capacity of 200 tonnes/day is economically attractive. Blue hydrogen from autothermal reforming has the lowest life cycle GHG emissions of 3.91 kgCO2eq/kg H2 followed by blue hydrogen from NGD (4.54 kgCO2eq/kg H2) SMR-85% (6.66 kgCO2eq/kg H2) and SMR-52% (8.20 kgCO2eq/kg H2). The findings of this study are useful for decision-making at various levels.

Currently hydrogen is mainly produced through steam reforming of natural gas. However this conventional process involves environmental and energy security concerns. This has led to the development of alternative technologies for (potentially) green hydrogen production. In this work the environmental and energy performance of biohydrogen produced in Europe via steam reforming of glycerol and bio-oil is evaluated from a life-cycle perspective and contrasted with that of conventional hydrogen from steam methane reforming. Glycerol as a by-product from the production of rapeseed biodiesel and bio-oil from the fast pyrolysis of poplar biomass are considered. The processing plants are simulated in Aspen Plus® to provide inventory data for the life cycle assessment. The environmental impact potentials evaluated include abiotic depletion global warming ozone layer depletion photochemical oxidant formation land competition acidification and eutrophication. Furthermore the cumulative (total and non-renewable) energy demand is calculated as well as the corresponding renewability scores and life-cycle energy balances and efficiencies of the biohydrogen products. In addition to quantitative evidence of the (expected) relevance of the feedstock and impact categories considered results show that poplar-derived bio-oil could be a suitable feedstock for steam reforming in contrast to first-generation bioglycerol.

Hydrogen is regarded to be one of the most promising renewable and clean energy sources. Finding a highly efficient and cost-effective catalyst to generate hydrogen via water splitting has become a research hotspot. Two-dimensional materials with exotic structural and electronic properties have been considered as economical alternatives. In this work 2D SnSe films with high quality of crystallinity were grown on a mica substrate via molecular beam epitaxy. The electronic property of the prepared SnSe thin films can be easily and accurately tuned in situ by three orders of magnitude through the controllable compensation of Sn atoms. The prepared film normally exhibited p-type conduction due to the deficiency of Sn in the film during its growth. First-principle calculations explained that Sn vacancies can introduce additional reactive sites for the hydrogen evolution reaction (HER) and enhance the HER performance by accelerating electron migration and promoting continuous hydrogen generation which was mirrored by the reduced Gibbs free energy by a factor of 2.3 as compared with the pure SnSe film. The results pave the way for synthesized 2D SnSe thin films in the applications of hydrogen production.

The computational thermodynamic analysis of a samarium oxide-based two-step solar thermochemical water splitting cycle is reported. The analysis is performed using HSC chemistry software and databases. The first (solar-based) step drives the thermal reduction of Sm2O3 into Sm and O2. The second (non-solar) step corresponds to the production of H2 via a water splitting reaction and the oxidation of Sm to Sm2O3. The equilibrium thermodynamic compositions related to the thermal reduction and water splitting steps are determined. The effect of oxygen partial pressure in the inert flushing gas on the thermal reduction temperature (TH) is examined. An analysis based on the second law of thermodynamics is performed to determine the cycle efficiency (ηcycle) and solar-to-fuel energy conversion efficiency (ηsolar´to´fuel) attainable with and without heat recuperation. The results indicate that ηcycle and ηsolar´to´fuel both increase with decreasing TH due to the reduction in oxygen partial pressure in the inert flushing gas. Furthermore the recuperation of heat for the operation of the cycle significantly improves the solar reactor efficiency. For instance in the case where TH = 2280 K ηcycle = 24.4% and ηsolar´to´fuel = 29.5% (without heat recuperation) while ηcycle = 31.3% and ηsolar´to´fuel = 37.8% (with 40% heat recuperation).

There is significant interest in Australia both federally and at the state level to develop a hydrogen production industry. Australia’s Chief Scientist Alan Finkel recently prepared a briefing paper for the COAG Energy Council outlining a road map for hydrogen. It identifies hydrogen has the potential to be a significant source of export revenue for Australia in future years assist with decarbonising Australia’s economy and could establish Australia as a leader in low emission fuel production.

As part of the ongoing investigations into the hydrogen production potential of Australia Geoscience Australia has been commissioned by the Department of Industry Innovation and Science to develop heat maps that show areas with high potential for future hydrogen production. The study is technology agnostic in that it considers hydrogen production via electrolysis using renewable energy sources and also fossil fuel hydrogen coupled with carbon capture and storage (CCS). The heat maps presented in this work are synthesized from the key individual national-scale datasets that are relevant for hydrogen production. In the case of hydrogen from electrolysis renewable energy potential and the availability of water are the most important factors with various infrastructural considerations playing a secondary role. In the case of fossil fuel hydrogen proximity to gas and coal resources water and availability of carbon storage sites are the important parameters that control the heat maps. In this report we present 5 different heat map scenarios reflecting different assumptions in the geospatial analysis and also reflecting to some degree the different projected timeframes for hydrogen production. The first three scenarios pertain to renewable energy and hydrogen There is significant interest in Australia both federally and at the state level to develop a hydrogen production industry. In August 2018 Australia’s Chief Scientist Dr Alan Finkel prepared a briefing paper for the COAG Energy Council outlining a road map for hydrogen. It identifies hydrogen has the potential to be a significant source of export revenue for Australia in future years assist with decarbonising Australia’s economy and could establish Australia as a leader in low emission fuel production.

As part of ongoing investigations into the hydrogen production potential of Australia Geoscience Australia has been engaged by the Department of Industry Innovation and Science to develop maps that show areas with high potential for future hydrogen production. The study is technology agnostic but considers only low carbon production processes. It includes hydrogen production via electrolysis using renewable energy sources (referred to as renewable hydrogen) as well as fossil fuel-derived hydrogen coupled with carbon capture and storage (CCS) (referred to as CCS hydrogen). The maps presented in this work are synthesized from the key individual national-scale datasets that are relevant for hydrogen production. In the case of hydrogen from electrolysis renewable energy potential (from wind solar and hydro resources) and the availability of water are the most important factors while various infrastructure considerations also play a role. In the case of CCS hydrogen proximity to gas and coal resources water and availability of carbon storage sites are the important parameters that control the spatial distribution of potential hydrogen production. In this report we present five different scenarios that reflect key differences in technologies for hydrogen production and the requirements of those technologies. Using geospatial analysis each scenario is translated into a heat map that shows regional trends in potential for hydrogen production based on access to underpinning resources and existing infrastructure.

Three scenarios explore the future potential for renewable hydrogen produced by electrolysis. These demonstrate a high potential for hydrogen production in the future near many Australian coastal areas which is even larger if infrastructure is available to transport renewable power generated from inland areas to the coast. Results also show significant future potential for hydrogen production in inland areas where water is available. The final two scenarios focus on the future potential for CCS hydrogen: a 2030 scenario and a 2050 scenario. A key factor in future CCS hydrogen potential is related to the timeframes for the availability of geological storage resources for CO_2.

Harnessing solar energy and converting it into renewable fuels by chemical processes such as water splitting and carbon dioxide (CO₂ ) reduction is a highly promising yet challenging strategy to mitigate the effects arising from the global energy crisis and serious environmental concerns. In recent years covalent organic framework (COF)-based materials have gained substantial research interest because of their diversified architecture tunable composition large surface area and high thermal and chemical stability. Their tunable band structure and significant light absorption with higher charge separation efficiency of photoinduced carriers make them suitable candidates for photocatalytic applications in hydrogen (H₂) generation CO₂ conversion and various organic transformation reactions. In this article we describe the recent progress in the topology design and synthesis method of COF-based nanomaterials by elucidating the structure-property correlations for photocatalytic hydrogen generation and CO₂ reduction applications. The effect of using various kinds of 2D and 3D COFs and strategies to control the morphology and enhance the photocatalytic activity is also summarized. Finally the key challenges and perspectives in the field are highlighted for the future development of highly efficient COF-based photocatalysts.

In this perspective on hydrogen carriers we focus on the needs for the development of robust active catalysts for the release of H₂ from aqueous formate solutions which are non-flammable non-toxic thermally stable and readily available at large scales at reasonable cost. Formate salts can be stockpiled in the solid state or dissolved in water for long term storage and transport using existing infrastructure. Furthermore formate salts are readily regenerated at moderate pressures using the same catalyst as for the H₂ release. There have been several studies focused on increasing the activity of catalysts to release H₂ at moderate temperatures i.e. < 80 °C below the operating temperature of a proton exchange membrane (PEM) fuel cell. One significant challenge to enable the use of aqueous formate salts as hydrogen carriers is the deactivation of the catalyst under operating conditions. In this work we provide a review of the most efficient heterogeneous catalysts that have been described in the literature their proposed modes of deactivation and the strategies reported to reactivate them. We discuss potential pathways that may lead to deactivation and strategies to mitigate it in a variety of H₂ carrier applications. We also provide an example of a potential use case employing formate salts solutions using a fixed bed reactor for seasonal storage of energy for a microgrid application.

In this present investigation a packed-filter bioreactor was employed to produce hydrogen utilizing an expired soft drink as a substrate. The effects of feeding substrate concentrations ranging from 19.51 10.19 5.34 3.48 to 2.51 g total sugar/L were examined and the position of the packed filter installed in the bioreactor at dimensionless heights (h/H) of 1/4 2/4 3/4 and 4/4 was studied. The results revealed that with a substrate concentration of 20 g total sugar/L and a hydraulic retention time (HRT) of 1 h a packed filter placed at the half-height position of the bioreactor (h/H 2/4) has the optimal hydrogen production rate hydrogen yield and average biomass concentration in the bioreactor resulting in 55.70 ± 2.42 L/L/d 0.90 ± 0.06 mol H₂/mol hexose and 17.86 ± 1.09 g VSS/L. When feeding substrate concentrations varied from 20 10 to 5 g total sugar/L with the packed-filter position at h/H 2/4 Clostridium sp. Clostridium tyrobutyricum and Bifidobacterium crudilactis were the predominant bacteria community. Finally it was discovered that the packed-filter bioreactor can produce stable hydrogen in high-strength organic effluent.

The most profitable offshore energy resources are usually found away from the coast. Nevertheless the accessibility and grid integration in those areas are more complicated. To avoid this problematic large scale hydrogen production is being promoted for far offshore applications. The main objective of this paper is to analyze the ability of wave energy converters to maximize hydrogen production in hybrid wind and wave far offshore farms. To that end wind and wave resource data are obtained from ERA5 for different locations in the Atlantic ocean and a Maximum Covariance Analysis is proposed for the selection of the most representative locations. Furthermore the suitability of different sized wave energy converters for auxiliary hydrogen production in the far offshore wind farms is also analysed. On that account the hydrodynamic parameters of the oscillating bodies are obtained via simulations with a Boundary Element Method based code and their operation is modelled using the software tool Matlab. The combination of both methodologies enables to perform a realistic assessment of the contribution of the wave energy converters to the hydrogen generation of an hybrid energy farm especially during those periods when the wind turbines would be stopped due to the variability of the wind. The obtained results show a considerable hydrogen generation capacity of the wave energy converters up to 6.28% of the wind based generation which could remarkably improve the efficiency of the far offshore farm and bring important economical profit. Wave energy converters are observed to be most profitable in those farms with low covariance between wind and waves where the disconnection times of the wind turbines are prone to be more prolonged but the wave energy is still usable. In such cases a maximum of 101.12 h of equivalent rated production of the wind turbine has been calculated to be recovered by the wave energy converters.

Chemical looping with iron-based oxygen carriers enables the production of hydrogen from various fossil and biogenic primary energy sources. In applications with real producer gases such as biogas or gasified biomass hydrogen sulfide represents one of the most challenging contaminants. The impact of H2S on the reactivity of a Fe2O3/Al2O3 oxygen carrier material in chemical looping hydrogen production was investigated in the present work. First potential sulfur deactivation mechanisms are discussed in detail on the basis of thermodynamic data. Afterwards an experimental study in a fixed-bed reactor system gave experimental evidence on the fate of sulfur in chemical looping hydrogen systems. The chemisorption of hydrogen sulfide (H2S) was identified as the main cause for the accumulative adsorption of H2S in the reduction phase and was confirmed by ex-situ ICP-EOS analysis. In the subsequent steam oxidation step significant quantities of H2S were released resulting in an undesirable contamination of the hydrogen product gas. The reason was found as weakened sulfur bonds through increasing reactor temperatures caused by the exothermic oxidation reactions. In additional air oxidation steps no further contaminants as sulfur dioxide were identified. A profound interpretation was achieved through the fulfillment of the overall sulfur mass balance within a mean deviation of 3.7%. Quantitative investigations showed that the hydrogen consumption decreased by 12% throughout the reduction phase in the event of 100 ppm H2S in the feed gas

Hydrogen sourced from energy recovery processes and conversion of waste materials is a method of providing both a clean fuel and a sustainable waste management alternative to landfill and incineration. The question is whether waste-to–hydrogen can become part of the zero-carbon future energy mix and serve as one of the cleaner hydrogen sources which is economically viable and environmentally friendly. This work critically assessed the potential of waste as a source of hydrogen production via various thermochemical (gasification and pyrolysis) and biochemical (fermentation and photolysis) processes. Research has shown hydrogen production yields of 33.6 mol/kg and hydrogen concentrations of 82% from mixed waste feedstock gasification. Biochemical methods such as fermentation can produce hydrogen up to 418.6 mL/g. Factors including feedstock quality process requirements and technology availability were reviewed to guide technology selection and system design. Current technology status and bottlenecks were discussed to shape future development priorities. These bottlenecks include expensive production and operation processes heterogeneous feedstock low process efficiencies inadequate management and logistics and lack of policy support. Improvements to hydrogen yields and production rates are related to feedstock processing and advanced energy efficiency processes such as torrefaction of feedstock which has shown thermal efficiency of gasification up to 4 MJ/kg. This will affect the economic feasibility and concerns around required improvements to bring the costs down to allow waste to viewed as a serious competitor for hydrogen production. Recommendations were also made for financially competitive waste-to-hydrogen development to be part of a combined solution for future energy needs.

For a green economy to be possible in the near future hydrogen production from water is a sought-after alternative to fossil fuels. It is however important to put things into context with respect to global CO2 emission and the role of hydrogen in curbing it. The present world annual production of hydrogen is about 70 million metric tons of which almost 50% is used to make ammonia NH3 (that is mostly used for fertilizers) and about 15% is used for other chemicals [1]. The hydrogen produced worldwide is largely made by steam CH4 reforming (SMR) which is one of the most energy-intensive processes in the chemical industry [2]. It releases based on reaction stoichiometry 5.5 kg of CO2 per 1 kg of H2 (CH4+ 2 H2O → CO2 + 4 H2). When the process itself is taken into account in addition the production [3] becomes about 9 kg of CO2 per kg of H2 and this ratio can be as high as 12 [4]. This results in the production of about one billion tons/year of CO2. The world annual CO2 emission from fossil fuels is however much larger: it is about 36 billion tons of which roughly 25% is emitted while generating electricity and heat 20% due to transport activity and 20% from other industrial processes. Because of the link between global warming and CO2 emissions there is an increasing move towards finding alternative approaches for energy vectors and their applications.

Gasification of municipal solid waste (MSW) with subsequent utilization of syngas in gas engines/turbines and solid oxide fuel cells can substantially increase the power generation of waste-to-energy facilities and optimize the utilization of wastes as a sustainable energy resources. However purification of syngas to remove multiple impurities such as particulates tar HCl alkali chlorides and sulfur species is required. This study investigates the feasibility of high temperature purification of syngas from MSW gasification with the focus on catalytic tar reforming and desulfurization. Syngas produced from a downdraft fixed-bed gasifier is purified by a multi-stage system. The system comprises of a fluidized-bed catalytic tar reformer a filter for particulates and a fixed-bed reactor for dechlorination and then desulfurization with overall downward cascading of the operating temperatures throughout the system. Novel nano-structured nickel catalyst supported on alumina and regenerable Ni-Zn desulfurization sorbent loaded on honeycomb are synthesized. Complementary sampling and analysis methods are applied to quantify the impurities and determine their distribution at different stages. Experimental and thermodynamic modeling results are compared to determine the kinetic constraints in the integrated system. The hot purification system demonstrates up to 90% of tar and sulfur removal efficiency increased total syngas yield (14%) and improved cold gas efficiency (12%). The treated syngas is potentially applicable in gas engines/turbines and solid oxide fuel cells based on the dew points and concentration limits of the remaining tar compounds. Reforming of raw syngas by nickel catalyst for over 20 h on stream shows strong resistance to deactivation. Desulfurization of syngas from MSW gasification containing significantly higher proportion of carbonyl sulfide than hydrogen sulfide traces of tar and hydrogen chloride demonstrates high performance of Ni-Zn sorbents.

Proton exchange membrane water electrolysis (PEMWE) is a key technology for future sustainable energy systems. Proton exchange membrane (PEM) electrolysis cells use iridium one of the scarcest elements on earth as catalyst for the oxygen evolution reaction. In the present study the expected iridium demand and potential bottlenecks in the realization of PEMWE for hydrogen production in the targeted GW a−1 scale are assessed in a model built on three pillars: (i) an in-depth analysis of iridium reserves and mine production (ii) technical prospects for the optimization of PEM water electrolyzers and (iii) PEMWE installation rates for a market ramp-up and maturation model covering 50 years. As a main result two necessary preconditions have been identified to meet the immense future iridium demand: first the dramatic reduction of iridium catalyst loading in PEM electrolysis cells and second the development of a recycling infrastructure for iridium catalysts with technical end-of-life recycling rates of at least 90%.

Hydrogen is an environmentally friendly biofuel which if widely used could reduce atmospheric carbon dioxide emissions. The main barrier to the widespread use of hydrogen for power generation is the lack of technologically feasible and—more importantly—cost‐effective methods of production and storage. So far hydrogen has been produced using thermochemical methods (such as gasification pyrolysis or water electrolysis) and biological methods (most of which involve anaerobic digestion and photofermentation) with conventional fuels waste or dedicated crop biomass used as a feedstock. Microalgae possess very high photosynthetic efficiency can rapidly build biomass and possess other beneficial properties which is why they are considered to be one of the strongest contenders among biohydrogen production technologies. This review gives an account of present knowledge on microalgal hydrogen production and compares it with the other available biofuel production technologies.

Producing hydrogen from water using a redox mediator on solid electrocatalyst particles in a reactor offers several advantages over classical electrolysis in terms of safety membrane degradation purity and flexibility. Herein vanadium-mediated hydrogen evolution on a commercial and low-cost Mo2C electrocatalyst is studied through the development of a reaction kinetics model. Based on a proposed mechanistic reaction scheme we established a kinetic rate law dependent on the concentration of V2+ the state-of-charge of the vanadium electrolyte from a vanadium redox flow battery and the amount of available catalytic sites on solid Mo2C. Kinetic experiments in transient conditions reveals a first-order dependence on both the concentration of V2+ and the concentration of catalytic active sites and a power law with an exponential factor of 0.57 was measured on the molar ratio V2+/V3+ i.e. on the electrochemical driving force generated on the Mo2C particles. The kinetic rate law was validated by studying the rate of reaction in steady-state conditions using a specially developed rotating ring-disk device (RRD) methodology. The kinetic model was demonstrated to be a useful tool to predict the hydrogen production via the chemical oxidation of V2+ over Mo2C at low pH (> 1 M H2SO4). For a perspective the model was implemented in a semi-batch reactor. The simulations highlight the optimal state-of-charge (SOC) to carry out the reaction in an efficient way for a given demand in hydrogen.

Industrial hydrogen production via alkaline water electrolysis (AEL) is a mature hydrogen production method. One argument in favor of AEL when supplied with renewable energy is its environmental superiority against conventional fossil-based hydrogen production. However today electricity from the national grid is widely utilized for industrial applications of AEL. Also the ban on asbestos membranes led to a change in performance patterns making a detailed assessment necessary. This study presents a comparative Life Cycle Assessment (LCA) using the GaBi software (version 6.115 thinkstep Leinfelden-Echterdingen Germany) revealing inventory data and environmental impacts for industrial hydrogen production by latest AELs (6 MW Zirfon membranes) in three different countries (Austria Germany and Spain) with corresponding grid mixes. The results confirm the dependence of most environmental effects from the operation phase and specifically the site-dependent electricity mix. Construction of system components and the replacement of cell stacks make a minor contribution. At present considering the three countries AEL can be operated in the most environmentally friendly fashion in Austria. Concerning the construction of AEL plants the materials nickel and polytetrafluoroethylene in particular used for cell manufacturing revealed significant contributions to the environmental burden.

The use of hydrogen as energy carrier is a promising option to decarbonize both energy and transport sectors. This paper presents an advanced techno-economic model for calculation of optimal dispatch of large-scale multi MW electrolysis plants in order to obtain a more accurate evaluation of the feasibility of business cases related to the supply of this fuel for different end uses combined with grid services' provision. The model is applied to the Spanish case using different scenarios to determine the minimum demand required from the FCEV market so that electrolysis facilities featuring several MW result in profitable business cases. The results show that grid services contribute to the profitability of hydrogen production for mobility given a minimum but considerable demand from FCEV fleets.

In the last two years or so there has been increasing interest in hydrogen as an energy source in Australia and around the world. Notably this is not the first time that hydrogen has caught our collective interest. Most recently the 2000s saw a substantial investment in hydrogen research development and demonstration around the world. Prior to that the oil crises of the 1970s also stimulated significant investment in hydrogen and earlier still the literature on hydrogen was not lacking. And yet the hydrogen economy is still an idea only.<br/>So what if anything might be different this time?<br/>This is an important question that we all need to ask and for which the author can only give two potential answers. First our need to make dramatic reductions in greenhouse gas (GHG) emissions has become more pressing since these previous waves of interest. Second renewable energy is considerably more affordable now than it was before and it has consistently outperformed expectations in terms of cost reductions by even its strongest supporters.<br/>While this dramatic and ongoing reduction in the cost of renewables is very promising our need to achieve substantial GHG emission reductions is the crucial challenge. Moreover meeting this challenge needs to be achieved with as little adverse social and economic impact as possible.<br/>When considering what role hydrogen might play we should first think carefully about the massive scale and complexity of our global energy system and the typical prices of the major energy commodities. This provides insights into what opportunities hydrogen may have. Considering a temperate country with a small population like Australia we see that domestic natural gas and transport fuel markets are comparable to and even larger than the electricity market on an energy basis.

The potentials of phenolic productions from lignin and black liquor (BL) via hydrothermal technology with the aids of alkalis and hydrogen donors were investigated by conducting batch experiments in micro-tube reactors with 300 °C sub-critical water as the solvent. The results showed that all the employed alkalis improved lignin degradation and thus phenolics production and the strong alkalis additionally manifested deoxygenation to produce more phenolics free of methoxyl group(s). Relatively hydrogen donors more visibly facilitated phenolics formation. Combination of strong alkali and hydrogen donors exhibited synergistically positive effects on producing phenolics (their total yield reaching 22 wt%) with high selectivities to phenolics among which the yields of catechol and cresols respectively peaked 16 and 3.5 wt%. BL could be hydrothermally converted into phenolics at high yields (approaching 10 wt% with the yields of catechol and cresols of about 4 and 2 wt% respectively) with the aids of its inherent alkali and hydrogen donors justifying its cascade utilization.