Publications

Hydrogen produced by renewable sources represents an interesting way to reduce the energetic dependence on fossil fuels in the transportation sector. This paper shows a feasibility study for the production storage and distribution of hydrogen in the western Sicilian context using three different renewable sources: wind biomass and sea wave. The objective of this study is the evaluation of the hydrogen demand needed to replace all diesel supplied buses with electrical buses equipped with fuel cells. An economic analysis is presented with the evaluation of the avoidable greenhouse gas emissions. Four different scenarios correlate the hydrogen demand for urban transport to the renewable energy resources present in the territories and to the modern technologies available for the production of hydrogen. The study focuses on the possibility of tapping into the potential of renewable energies (wind biomass and sea wave) for the production of hydrogen by electrolysis. The use of hydrogen would reduce significantly the emissions of particulate and greenhouse gases in the urban districts under analysis.

Visible-light-driven hydrogen production through photocatalysis has attracted enormous interest owing to its great potential to address energy and environmental issues. However photocatalysis possesses several limitations to overcome for practical applications such as low light absorption efficiency rapid charge recombination and poor stability of photocatalysts. Here the preparation of efficient noble metal–semiconductor hybrid photocatalysts for photocatalytic hydrogen production is presented. The prepared ternary Rh–TiO₂–CeO₂ hybrid photocatalysts exhibited excellent photocatalytic performance toward the hydrogen production reaction compared with their counterparts ascribed to the synergistic combination of Rh TiO₂ and CeO₂.

Under the dual pressure of energy conservation and environmental protection the internal combustion engine industry is facing huge challenges and it is imperative to find new clean energy. Hydrogen energy is expected to replace traditional fossil fuels as an excellent fuel for internal combustion engines because of its clean continuous regeneration and good combustion performance. This review article focuses on the research and development of blended hydrogen-fuel internal combustion engines in China since the beginning of this century. The main achievements gained by Chinese researchers in performing research on the effects of the addition of hydrogen into engines which predominantly include many types of hydrogen-blended engines such as gasoline diesel natural gas and alcohol engines rotary engines are discussed and analyzed in these areas of the engine’s performance and the combustion and emission characteristics etc. The merits and demerits of blended hydrogen-fuel internal combustion engines could be concluded and summarized after discussion. Finally the development trend and direction of exploration on hydrogen-fuel internal combustion engines could also be forecasted for relevant researchers.

The Reverse electrodialysis heat engine (REDHE) combines a reverse electrodialysis stack for power generation with a thermal regeneration unit to restore the concentration difference of the salt solutions. Current approaches for converting low-temperature waste heat to electricity with REDHE have not yielded conversion efficiencies and profits that would allow for the industrialization of the technology. This review explores the concept of Heat-to-Hydrogen with REDHEs and maps crucial developments toward industrialization. We discuss current advances in membrane development that are vital for the breakthrough of the RED Heat Engine. In addition the choice of salt is a crucial factor that has not received enough attention in the field. Based on ion properties relevant for both the transport through IEMs and the feasibility for regeneration we pinpoint the most promising salts for use in REDHE which we find to be KNO3 LiNO3 LiBr and LiCl. To further validate these results and compare the system performance with different salts there is a demand for a comprehensive thermodynamic model of the REDHE that considers all its units. Guided by such a model experimental studies can be designed to utilize the most favorable process conditions (e.g. salt solutions).

Natural gas based hydrogen production with carbon capture and storage is referred to as blue hydrogen. If substantial amounts of CO2 from natural gas reforming are captured and permanently stored such hydrogen could be a low-carbon energy carrier. However recent research raises questions about the effective climate impacts of blue hydrogen from a life cycle perspective. Our analysis sheds light on the relevant issues and provides a balanced perspective on the impacts on climate change associated with blue hydrogen. We show that such impacts may indeed vary over large ranges and depend on only a few key parameters: the methane emission rate of the natural gas supply chain the CO2 removal rate at the hydrogen production plant and the global warming metric applied. State-of-the-art reforming with high CO2 capture rates combined with natural gas supply featuring low methane emissions does indeed allow for substantial reduction of greenhouse gas emissions compared to both conventional natural gas reforming and direct combustion of natural gas. Under such conditions blue hydrogen is compatible with low-carbon economies and exhibits climate change impacts at the upper end of the range of those caused by hydrogen production from renewable-based electricity. However neither current blue nor green hydrogen production pathways render fully “net-zero” hydrogen without additional CO2 removal.

Power to gas (PtG) is an emerging technology that allows to overcome the issues due to the increasingly widespread use of intermittent renewable energy sources (IRES). Via water electrolysis power surplus on the electric grid is converted into hydrogen or into synthetic natural gas (SNG) that can be directly injected in the natural gas network for long-term energy storage. The core units of the Power to synthetic natural gas (PtSNG) plant are the electrolyzer and the methanation reactors where the renewable electrolytic hydrogen is converted to synthetic natural gas by adding carbon dioxide. A technical issue of the PtSNG plant is the different dynamics of the electrolysis unit and the methanation unit. The use of a hydrogen storage system can help to decouple these two subsystems and to manage the methanation unit for assuring long operation time and reducing the number of shutdowns. The purpose of this paper is to evaluate the energy storage potential and the technical feasibility of the PtSNG concept to store intermittent renewable sources. Therefore different plant sizes (1 3 and 6 MW) have been defined and investigated by varying the ratio between the renewable electric energy sent to the plant and the total electric energy generated by the renewable energy source (RES) facility based on a 12 MW wind farm. The analysis has been carried out by developing a thermochemical and electrochemical model and a dynamic model. The first allows to predict the plant performance in steady state. The second allows to forecast the annual performance and the operation time of the plant by implementing the control strategy of the storage unit. The annual overall efficiencies are in the range of 42–44% low heating value (LHV basis). The plant load factor i.e. the ratio between the annual chemical energy of the produced SNG and the plant capacity results equal to 60.0% 46.5% and 35.4% for 1 3 and 6 MW PtSNG sizes respectively.

Hydrogen (H2) internal combustion engines may represent cost-effective and quick solution to the issue of the road transport decarbonization. A major factor limiting their competitiveness relative to fuel cells (FC) is the lower efficiency. The present work aims to demonstrate the feasibility of a H2 engine with FC-like 60%+ brake thermal efficiency (BTE) levels using a double compression-expansion engine (DCEE) concept combined with a high pressure direct injection (HPDI) nonpremixed H2 combustion. Experimentally validated 3D CFD simulations are combined with 1D GT-Power simulations to make the predictions. Several modifications to the system design and operating conditions are systematically implemented and their effects are investigated. Addition of a catalytic burner in the combustor exhaust insulation of the expander dehumidification of the EGR and removal of the intercooling yielded 1.5 1.3 0.8 and 0.5%-point BTE improvements respectively. Raising the peak pressure to 300 bar via a larger compressor further improved the BTE by 1.8%-points but should be accompanied with a higher injector-cylinder differential pressure. The λ of ~1.4 gave the optimum tradeoff between the mechanical and combustion efficiencies. A peak BTE of 60.3% is reported with H2DCEE which is ~5%-points higher than the best diesel-fueled DCEE alternative.

The effect of alcohol structure on photocatalytic production of H₂ from C-3 alcohols was studied on 0.5% Pt/TiO₂. A C-2 alcohol (ethanol) was also included for comparative purposes. For individual reactions from 10% v/v aqueous solutions of alcohols hydrogen production followed the order ethanol ≈ propan-2-ol > propan-1- ol > propane-123-triol > propane-12-diol > propane-13-diol. The process was found to be quite sensitive to the presence of additional alcohols in the reaction medium as evidenced by competitive reactions. Therefore propan-2-ol conversion was retarded in the presence of traces of the other alcohols this effect being particularly significant for vicinal diols. Additional experiments showed that adsorption of alcohols on Pt/TiO₂ followed the order propane-123-triol > propane-12-diol > propane-13-diol > propan-1-ol > ethanol > propan-2-ol. Adsorption studies (DRIFT) and monitoring of reaction products showed that the main photocatalyzed process for propan-2-ol and propan-1-ol transformation is dehydrogenation to the corresponding carbonyl compound (especially for propan-2-ol both in the liquid and the gas phase). In the case of liquid-phase transformation of propan-1-ol ethane was also detected which is indicative of the dissociative mechanism to lead to the corresponding C-1 alkane. All in all competitive reactions proved to be very useful for mechanistic studies.

The actual start of the full-scale hydrogen energy infrastructure operations is scheduled to 2020 in Japan. The scope of factors and policy for the hydrogen infrastructure development in Japan is made. The paper provides observation for the major undergoing and already done projects for each link within hydrogen infrastructure chain – from production to end-user applications. Implications for the Russian energy policy are provided.

In the present paper the theoretical study of the un-stretched laminar premixed flames of hydrogen-methane mixtures is carried out by using the detailed reaction mechanism GRI-Mech 3.0 implemented in the CHEMKIN software to find out the effect of hydrogen addition on the hybrid fuel burning velocity. The model results show that the laminar burning velocity of the hydrogen-methane mixtures is not the linear regression of those of the pure fuels since it results substantially less than the proportional averaging of the values for the fuel constituents. Moreover the effect of hydrogen addition in terms of enhancement of the mixture laminar burning velocity with respect to the methane is relevant only at very high values of the hydrogen content in the hybrid mixtures (> 70 % mol.). The performed sensitivity analysis shows that these results can be attributed to kinetics and in particular to the concentration of H radicals: depending on the hydrogen content in the fuels mixture the production of the H radicals can affect the limiting reaction step for methane combustion. Two regimes are identified in the hydrogen-methane combustion. The first regime is controlled by the methane reactivity the hydrogen being not able to significantly affect the laminar burning velocity (< 70 % mol.). In the second regime the hydrogen combustion has a relevant role as its high content in the hybrid fuel leads to a significant H radicals pool thus enhancing the reaction rate of the more slowly combusting methane.