This publication explores current and prospective methods for hydrogen production and purification, with a strong emphasis on membrane-based technologies for purification and separation. This focus is justified by the ongoing shift towards renewable energy sources (RESs) in electricity generation, necessitating strategic changes to increase hydrogen utilization, particularly in the automotive, heavy road, and rail sectors, by 2025–2030. The adoption of hydrogen from RESs in the construction, energy, and industrial sectors (e.g., for process heat or fertilizer production) is also under consideration, driving the need for innovative production, separation, and purification methods. Historically, industrial-scale hydrogen has been predominantly derived from fossil fuels, but renewable sources such as electrolysis, biological, and thermal processes now offer alternatives with varying production efficiencies (0.06–80%) and gas compositions. Therefore, selecting appropriate separation and purification methods is critical based on specific usage requirements and the gas composition. Industrial-scale hydrogen purification commonly employs pressure swing adsorption (PSA) technologies, capable of achieving up to 99.99% purity. Cryogenic distillation is suitable for applications needing up to 95% purity. Membrane technologies, including polymer, metallic, and electrolytic membranes, have traditionally been limited to moderate volumes of pure gas production but are crucial for hydrogen purification and separation. This publication critically evaluates the potential of membrane technology for hydrogen separation, particularly in response to the anticipated rise in demand for RES-derived hydrogen, including from renewable feedstocks.

In the oil and gas industry, tracers are used to estimate residual oil saturation, to indicate the location and orientation of fractures in tight reservoirs, to identify and mark the direction of fluid flow in fractured deposits, to locate faults and discontinuities, and to measure fluid movement in injection wells during drilling. The tracers should behave in a mechanically similar manner to the tested substance, e.g., formation waters, oil or gas, and, on the other hand, they should significantly differ from them in terms of chemical properties so that it is possible to identify them. One of the fluorescent tracers used in the oil and gas industry, e.g., for inter-well tests during secondary or tertiary production methods (especially during reservoir hydration), is uranine. In order to assess the effectiveness of fluid movement measurements, it is necessary to determine the uranine content in formation waters. In this study, a method was developed to determine uranine in formation water samples using high-performance liquid chromatography with fluorescence detection (HPLC/FLD). The initial step in preparing samples for chromatographic analysis would be solid phase extraction (SPE). The method was validated and allows for the determination of uranine in formation water samples in the concentration range from 0.030 to 2.80 µg/L. The validation of the method included the analysis of factors influencing the measurement result (sources of uncertainty), determination of the linearity range of the standard curve, determination of the quantification limit of the method, and verification of the reproducibility, selectivity, stability and correctness achieved. The method developed within the study can be successfully applied in the case of the determination of uranine content in formation water samples from the oil and gas mining industry, which are often unstable and characterized by a relatively complex matrix. After validation, the method will also be applicable to the determination of uranine in matrices with a similar physicochemical composition, e.g., to assess groundwater flow in deformed carbonate aquifers or to characterize faults that act as barriers to horizontal groundwater flow.

The European Green Deal emphasizes the development of renewable energy sources to combat climate change. However, as photovoltaic expansion accelerates, so does the potential for increased waste, necessitating effective material recycling strategies. Indium, a scarce and valuable element crucial to the production of photovoltaic panels, underscores the necessity for efficient recycling practices to reduce reliance on virgin resources. In a recent laboratory analysis, a CIGS photovoltaic panel underwent a series of processes including crushing, grinding, and homogenization. The concentration of indium, vital for recycling, was meticulously analyzed using ICP-MS and validated through microscopic and composition analyses. Subsequent extraction utilizing 3 M HCl and H₂O₂, followed by electrolysis, yielded a remarkable up to 52% indium recovery within a 48-h timeframe. Importantly, the study encompassed both averaged panel samples and samples from the absorbing layer, emphasizing the comprehensive approach required for efficient recycling. This underscores the critical importance of optimizing recycling processes to mitigate the environmental impact associated with the disposal of photovoltaic panels. By maximizing indium recovery, not only are environmental impacts reduced, but the long-term sustainability of renewable energy technologies is also ensured. This highlights the interconnectedness of recycling practices with the broader goals of achieving a circular economy and securing the viability of renewable energy systems in the fight against climate change.

Significant amounts of produced water, spent drilling fluid, and drill cuttings, which differ in composition and characteristics in each drilling operation, are generated in the oil and gas industry. Moreover, the oil and gas industry faces many technological development challenges to guarantee a safe and clean environment and to meet strict environmental standards in the field of processing and disposal of drilling waste. Due to increasing application of nanomaterials in the oil and gas industry, drilling wastes may also contain nanometer-scale materials. It is therefore necessary to characterize drilling waste in terms of nanomaterial content and to optimize effective methods for their determination, including a key separation step. The purpose of this study is to select the appropriate method of separation and pre-concentration of silver nanoparticles (AgNPs) from drilling wastewater samples and to determine their size distribution along with the state of aggregation using single-particle inductively coupled plasma mass spectrometry (spICP-MS). Two AgNP separation methods were compared: centrifugation and cloud point extraction. The first known use of spICP-MS for drilling waste matrices following mentioned separation methods is presented.