This review examines the central role of hydrogen, particularly green hydrogen from renewable sources, in the global search for energy solutions that are sustainable and safe by design. Using the hydrogen square, safety measures across the hydrogen value chain—production, storage, transport, and utilisation—are discussed, thereby highlighting the need for a balanced approach to ensure a sustainable and efficient hydrogen economy. The review also underlines the challenges in safety assessments, points to past incidents, and argues for a comprehensive risk assessment that uses empirical modelling, simulation-based computational fluid dynamics (CFDs) for hydrogen dispersion, and quantitative risk assessments. It also highlights the activities carried out by our research group SaRAH (Safety, Risk Analysis, and Hydrogen) relative to a more rigorous risk assessment of hydrogen-related systems through the use of a combined approach of CFD simulations and the appropriate risk assessment tools. Our research activities are currently focused on underground hydrogen storage and hydrogen transport as hythane.

Energy and environmental issues are of great importance in the present era. The transition to renewable energy sources necessitates technological, political, and behavioral transformations. Hydrogen is a promising solution, and many countries are investing in the hydrogen economy. Global demand for hydrogen is expected to reach 120 million tonnes by 2024. The incorporation of hydrogen for efficient energy transport and storage and its integration into the transport sector are crucial measures. However, to fully develop a hydrogen-based economy, the sustainability and safety of hydrogen in all its applications must be ensured. This work describes and compares different technologies for hydrogen production, storage, and utilization (especially in fuel cell applications), with focus on the research activities under study at SaRAH group of the University of Naples Federico II. More precisely, the focus is on the production of hydrogen from bio-alcohols and its storage in formate solutions produced from renewable sources such as biomass or carbon dioxide. In addition, the use of materials inspired by nature, including biowaste, as feedstock to produce porous electrodes for fuel cell applications is presented. We hope that this review can be useful to stimulate more focused and fruitful research in this area and that it can open new avenues for the development of sustainable hydrogen technologies.

Biological treatments focused on stabilizing and detoxifying olive mill wastewater facilitate agronomic reuse for irrigation and fertilization. Anaerobic digestion is particularly attractive in view of energy recovery, but is severely hampered by the microbial toxicity of olive mill wastewater. In this work, the addition of biochar to the digestion mixture was studied to improve the stability and efficiency of the anaerobic process. Kinetics and yields of biogas production were evaluated in batch digestion tests with biochar concentrations ranging from 0 to 45 g L⁻¹. The addition of biochar reduced sensibly the lag phase for methanogenesis and increased the maximum rate of biogas generation. Final yields of hydrogen and methane were not affected. Upon addition of biochar, soluble COD removal increased from 66% up to 84%, and phenolics removal increased from 50% up to 95%. Digestate phytotoxicity, as measured by seed germination tests, was reduced compared to raw wastewater. Addition of biochar further reduced phytotoxicity and, furthermore, a stimulatory effect was observed for a twenty-fold dilution. In conclusion, biochar addition enhances the anaerobic digestion of olive mill wastewaters by effectively reducing methanogenesis inhibition and digestate phytotoxicity, thus improving energy and biomass recovery.

A sample of ETS-10 was prepared and characterized by spectroscopic (Raman, UV–vis, FT-IR) and TPD techniques. An interpretation of the vibrational spectra was proposed. Absorption in the UV–vis range was typical of charge-transfer transitions involving octahedral Ti. No surface –OH groups were detected on the dehydrated sample. FT-IR measurements showed that water was adsorbed in two different molecular modes while ammonia was adsorbed coordinatively and mostly desorbed below 600 K. These results were confirmed by TPD studies that showed hydrogen-bonded water and water coordinated to Na⁺ and K⁺ cations located in the main channels of ETS-10. Ammonia TPD measurements on the hydrated material provided evidence for two forms of adsorbed NH₃, both bonded to water molecules. On the anhydrous material, NH₃ was probably coordinated only to the more loosely bonded Na⁺ and K⁺ ions in the main channels of ETS-10. The amount of adsorbed NH₃ was markedly reduced after heat treatment that led to a partial loss of crystallinity.