1. Introduction
Annual global greenhouse gas (GHG) emissions have been increasing steadily since 1998 [
1]. This has contributed to the rise in global temperatures and sea levels. Climate change is a global threat to our way of life, and it changed our perspective on our role in the ecosystem. To keep up with increasing global energy demands and reduce our impact on the climate, a shift toward renewable sources is required. After signing the Paris Agreement, the European Union (EU) is “striving to be the first climate-neutral continent” with the European Green Deal package. First published in 2019, it is a comprehensive strategy with an ambitious set of initiatives to achieve net-zero GHG emissions by 2050 and to “improve the well-being and health of citizens and future generations”. In line with the goals of the Green Deal, the EU’s Hydrogen Strategy was published in 2020 [
2,
3]. Hydrogen is versatile in its applicability in many sectors, such as mobility, transport, power or heavy industry; it can be used as a fuel, an energy carrier or a feedstock. It is not a one-size-fits-all solution, but as part of an integrated energy system, it can have a significant role in the decarbonization of those sectors. On 18th of May 2022, the European Commission published the REPowerEU program to “reduce our dependence on Russian fossil fuels by fast-forwarding the clean transition...” [
4]. Scaling up the transition to renewable energy is key to accelerating the EU’s phasing out of Russian fossil fuels and achieving “...a more resilient energy system and a true Energy Union”. The report reemphasizes the role of hydrogen as a key component to replace natural gas, coal and oil in hard-to-decarbonize industries and transport. The target by 2030 is to produce 10 million tonnes of hydrogen domestically and import another 10 on top of that. For a hydrogen-ready infrastructure and the regulatory framework, standards have to be rolled out in an accelerated manner for a successful energy system transition. Hydrogen will have a crucial role in balancing a renewables-based electricity system and in seasonal storage, enhancing decarbonization and the security of supply. One example of the use of seasonal storage in the green hydrogen supply chain is shown in
Figure 1. When green electricity is cheap and abundant (e.g., in summer), the surplus energy can be used to produce hydrogen, i.e., transforming electrical to chemical energy. In winter, when solar power generation is low and heat demand is high, hydrogen can be recovered and used in heating appliances or fuel cells. This type of storage is preferential because energy-specific storage costs are much lower and significantly more energy can be stored, transported and distributed than in the form of electricity [
5]. As an energy carrier, hydrogen has the advantage that a portion of the existing gas grid could be repurposed for its transport.
Hydrogen could provide up to 24% of the total energy demand in the world by 2050, and large-scale underground storage (UGS) is essential to meet demands in the 2030–2050 period [
3]. There are three main options for UGS in natural formations: salt caverns, depleted gas fields and aquifers [
6]. Storage in salt caverns is a proven concept with in-operation sites for nearly 50 years in the USA (3) and UK (1), listed in
Table 1 [
7,
8,
9,
10]. In spite of only four active sites worldwide, the technology can be considered mature, but all these facilities serve as feedstock for the chemical industry with constant annual demand profiles. Seasonal balancing requires higher injection/withdrawal rates and a fast-paced, flexible and cyclic operation with its unique challenges to be addressed.
Although salt caverns are regarded as the ideal solution because of their natural tightness, suitable formations in Europe are mainly located in Northern Germany, Poland, Denmark and the UK, as illustrated in
Figure 2 from Caglayan et al. [
11]. Porous structures (depleted gas fields and aquifers) are more widely available across Europe. According to a report from 2021, there are 63 salt cavern sites with a total working capacity of 206 TWh, and there are 80 depleted gas reservoirs with a total working capacity of 792 TWh, showing the potential in depleted gas fields for underground hydrogen storage [
12,
13,
14].
Currently, there are no known projects where pure hydrogen is stored in a porous structure. Pilot and demonstration projects, as well as potential sites, were collected by Sambo et al. [
10]. Recent projects in Austria and Argentina showed that the injection and storage in natural gas reservoirs of up to 20% of hydrogen could be safely performed; meanwhile, the storage of pure hydrogen is currently being investigated in Austria [
15,
16,
17]. A storage facility does not consist only of the reservoir. It also needs wells for the injection/withdrawal, pipelines and gas processing equipment, including compression, drying and cleaning. In depleted gas fields, residual natural gas (a mixture of methane, hydrocarbons, carbon dioxide, nitrogen and more) contaminates the hydrogen. Quality requirements in the chemical industry or fuel cells are very strict and cannot be met without separation from contaminants. The most common technology for hydrogen purification is pressure swing adsorption (PSA).
Adsorption is the phenomenon when gas molecules attach to a solid to form bonds with the surface molecules having unbalanced forces, because they do not experience the same attraction from each side [
18]. Different gases have different affinities to adsorb on given solids, called adsorbents. In a pressure swing system, the fact that this affinity increases with increasing pressure is used. The process is reversible, i.e., the adsorbed species can be recovered and the adsorbent regenerated by pressure reduction. The first patented use of pressure swing adsorption on a commercial scale was for the separation of air by Skarstrom (1958) and Montgareuil and Dargan (1964) [
19,
20]. These two patents became the foundation for PSA separation technique commercialization in the following decades. Further details on adsorbents, processes, equilibria and kinetics can be found in the literature [
18,
21,
22,
23]. Key applications of PSA are the separation of air, CO
2 removal from steel mill reduction gas and hydrogen purification [
24]. Feed gas can be from various sources, including methanol plants, ethylene offgas, ammonia plants or cryogenic purification, but the most common use of PSA is the hydrogen recovery from steam methane reforming (SMR) offgas ([
23,
25,
26,
27,
28,
29,
30,
31]). The technology can be considered mature, but new challenges arise with seasonal storage in depleted natural gas fields. Namely, the decreasing pressure and hydrogen content throughout the operation, contrary to the state-of-the-art systems, where the feed parameters are constant. In this work, we designed a laboratory-scale PSA unit to measure the separation performance with a wide range of feed conditions to represent the recovery phase over the winter months.
2. Materials and Methods
As described in the introduction, the varying composition and pressure of the withdrawn gas is a significant challenge for purification and conditioning. The properties of the gas mixture can range in a wide interval when stored in a natural gas reservoir. A certain amount of cushion gas is required in the gas field, even after it is “emptied”, to prevent the crumbling of the porous structure. This limits the lowest achievable pressure in the extraction phase; meanwhile, the cap rock sealing integrity limits the maximum pressure. Both are specific to the storage site and require extensive testing before operation. There are currently two depleted gas fields in operation for hydrogen storage and a few potential sites where investigation has started. Sambo et al. collected and reviewed in-operation and potential sites, including salt caverns, depleted oil and gas fields and aquifers [
10]. This work focuses on the post-storage purification of the gas with a high-pressure PSA and transient feed conditions. As a result, a generalized underground natural gas field was investigated, with a pressure range of 25–60 bar and a composition of 98–65% hydrogen content. There are no data available for storing pure hydrogen in porous rock formations, so the range of feed parameters was approximated. The lower pressure limit was selected as a typical cushion gas pressure. The upper limit was selected to be close to the pipeline pressure of the gas grid system. The main component of natural gas is methane, so a binary mixture of methane and hydrogen was used in this work. Continuous operation and linear progression were assumed, and four distinct stages were selected to represent the month-long withdrawal process, as shown in
Figure 3. The first stage is at the start of withdrawal, where pressure is high, and only traces of natural gas (represented by methane in this work) are present. In the second stage, the pressure is still high, but the natural gas content is significantly larger. The third stage is moderately high pressure with moderate natural gas content. This is the closest feed gas composition to current state-of-the-art industrial processes. The final stage is at the end of withdrawal, with moderate pressures and high contaminant content. Numerical values for each stage are listed in
Table 2. In a real-world application, many more pressure–composition pairs occur, and the separation unit must work effectively through the whole range. As an early-stage, laboratory-scale investigation, the four defined stages are sufficient to distinguish between qualitative behaviours of mixtures and provide data to validate a process simulation model.
A laboratory-scale pressure swing adsorption unit with 4 (+1) beds was built for this purpose. Four beds were filled with Desorex 33C activated carbon, a 3 mm diameter cylindrical, commercial adsorbent from coconut shells, provided by
DonauChem. The fifth column serves as a reserve to protect the analysis equipment from the pressure of flow surges. The unit has three main components, illustrated in
Figure 4. A detailed P&ID of the experimental setup is available on request, but the description of the build, components used and testing are out of the scope of this work, rather an overview is provided:
The mixing station includes the gas cylinders inside a ventilated cabinet, the feed lines and a set of mass flow controllers (MFCs). Here, the gas mixture can be tailored to the experiment. Hydrogen and methane were used, and nitrogen was connected on the third line for flushing and inertization of the system.
The pressure swing adsorption unit consists of four carbon-filled pressure vessels, each with a set of valves for feed, offgas and product. All columns are connected to the crossflow panel for the interconnection of adsorbers in the depressurization, purging and pressurization steps. The central point of this panel is the manual needle valve, which allows for gradual pressure equalization. Each adsorber is equipped with a pressure sensor, filter and safety valves. This subunit of the system was scaled up to a pilot-sized plant, the correlation and scaling property being interstitial velocity.
The analysis section starts with an empty adsorber column on the product line, which serves as a buffer to protect the sensitive equipment from surges of flow or pressure. The product and offgas lines are equipped with pressure sensors and PID-controlled control valves to limit the flowrate. Then, both lines are routed to the flare under a closed fume hood to neutralize dangerous gases on atmospheric pressures. There are three routes for the gases to take to the flare: direct route, through the mass flow meter or the gas analyzer unit with gas sensors. An infrared sensor measures the methane, and the hydrogen is measured through temperature conductive capacity in the same unit.
2.1. Experimental Work
Numerous experiments were conducted for each stage while modifying the most important parameters. A complete list is shown in
Table 3. Experiments with the most stable pressure and flow control and lowest methane appearance in the product stream were selected as the best runs. These are highlighted in the table and evaluated in the next section.
Feed composition and adsorption pressure are linked to the stages defined previously. The cycle times and purge-to-feed ratios were varied slightly; meanwhile, the step times were changed and modified significantly. The step sequence is listed in
Table 4. This work focuses on the applicability of PSA for hydrogen purification with transient feed conditions from underground storage; the detailed steps of process design are not provided.
2.2. Product Purity
The purity of the product hydrogen is a crucial parameter when describing the quality of the purification process. Many applications, especially recently built or upgraded gas powerplants and residential appliances, are prepared to operate with blends (natural gas–hydrogen mixtures). On the other hand, many applications require high-purity hydrogen, most notably fuel cells. International standards from 2019 and 2020 (ISO 14687:2019, SAE J2719-202003) regulate the concentration of 14 impurities specifically, not just the mole fraction of the hydrogen product. These limits are listed in
Table 5 [
32].
There are several methods to assess purity, depending on what data are available. In this work, the momentary molar fraction is equated to purity. The same definition is used throughout literature, and it is calculated through the following equation [
33]:
where
C is the volume fraction and
Q is the volume flow of hydrogen in the numerator and all components, noted as
j, in the denominator. The subscript
P notes the product side of the columns.
2.3. Hydrogen Recovery
The recovery factor of hydrogen is a critical parameter in gas separation. In this process, the absolute quantity of recovered hydrogen can be converted into energy. This energy has to be greater than the energy put in the storage and withdrawal to make it economically feasible for seasonal balancing. It is not worth operating a plant that requires net energy input. On the other hand, as long as the net energy is positive, the recovery factor does not matter because the energy used for the production, compression and storage was surplus renewable energy. We estimated that a recovery factor of 0.8 should result in net energy positive and set as a target in long-term operations. The recovery factor in this study is only based on material balancing, which is not an accurate form of definition. However, it gives an indication and allows the comparison of different stages.
where
C is the volume fraction and
Q is the volume flow of hydrogen. The subscript
P notes the product side of the columns and subscript
F the feed values.
4. Discussion
Each of the four experiments represents a stage in the withdrawal phase of underground, seasonal energy storage in the form of hydrogen. The results show that pressure swing adsorption can be a viable and effective method for the purification of the contaminated hydrogen, even with transient feed conditions or at high pressures. The sizing of the adsorbers was well chosen because, even in the last stage, an easy-to-control process could be implemented, and no rapid PSA mode was needed. At the same time, the unit was also operable in the first stage, where the pressure was high, and the methane content of the feed was low without the excessive need for purging. A key finding is that in this region, the high absolute pressure and the high pressure difference between adsorbers did not cause the erosion of the adsorbent or any irreversible effect in the adsorption–desorption process.
The process did not come without its challenges. Most issues resulted from the system build, i.e., the use of on/off valves and the common line for the pressure equalization and pressurization by-product. This consistently caused a pressure drop in the adsorption step, which widened the mass transfer zone and advanced the concentration front ahead of the planned bed length. Consequently, the gradual decrease in the purity cycle to cycle was seen even in just a few cycles, particularly in the stage three experiment. This error was successfully mitigated in the stage one experiment with the proper setting of the manual needle valve in the pressure equalization line. The subsequent measurements show that the same setting was insufficient in other stages, and no balance was found with the implemented step times. It shows that the process design for a PSA system is complex, and the parameters are heavily interconnected. Transient feed conditions emphasize this challenge because the physical components and step sequence have to be selected for various processes. It is advised to use proportional control valves instead of solenoids. In the case of a four-adsorber system, like the laboratory setup, this would require 16 proportional valves with a wide range of operating conditions. Such components are rarely available off the shelf and significantly increase the separation unit’s capital cost.
While the range of parameters can be estimated with high confidence, their exact progress in the months-long process is difficult to estimate. The four stages defined in this work are qualitative representations. In a continuous operation, changes in the pressure and composition would be continuous. In the case of an on-demand operation, the feed parameters could change drastically between startups. Both use cases require a flexible, adaptive process control strategy. An experimental investigation is time and resource-consuming, and optimizing each possibility is impossible. The present experimental cases are planned to be paired with a dynamic or cyclic steady-state simulation to expand the investigation and optimize the cycle for the withdrawal phase.
5. Conclusions
Long-term energy storage is of considerable interest in research and industry alike. One often-discussed idea was outlined in this research, in which surplus renewable electricity is converted to hydrogen by electrolysis, inserted into a depleted gas field and recovered when demand is high. The cushion gas (present in the porous rock formation for structural support) was assumed to be methane. The research focused on the technological feasibility of recovering hydrogen from the mixture, employing pressure swing adsorption (PSA). The withdrawal process can continue over several months, over which the pressure in the reservoir decreases and the composition of the mixture varies. The pressure range was selected between the cushion gas and gas grid pressure (25–60 bar). The composition range was selected to be between 65 and 98% hydrogen. Four distinct stages were defined within this range for investigation. A four-bed, lab-scale PSA unit and a 12-step process were developed, and cyclic experiments were conducted to evaluate the separation performance. The pressure profiles of each adsorber, product composition and flowrates were measured, and the product purity and recovery were calculated for evaluation. This is the first investigation of a PSA system with changing feedstock conditions and high pressures. The results indicate a viable performance, as the hydrogen purity did not change between stages and the recovery factor decreased slightly with lower pressures and hydrogen content. The process performance was not uniform, especially in stage two, where the recovery was lower than in the subsequent stage. Minor shortcomings of the system were recognized early, but they did not hinder the production of reliable results. The use of solenoid valves introduced unintended pressure changes within the process, and the accuracy of the gas analytics system did not reach analytical standards. A hydrogen purity of 99.95% was achieved in all stages, and the average hydrogen recovery ranged between 60 and 80%. The results support the feasibility of a single PSA system for the on-site separation from methane and suggest that fuel-cell-quality hydrogen can be produced during the recovery period.
A further investigation into mixtures with different parameters should be conducted either experimentally or in the form of a process simulation. The four stages defined here include four distinct feedstock parameters, but they are insufficient to support the process control design for a scaled system. The following steps in the research include the development of a process simulation model using the results of this research as a validation case and designing a process control system for a pilot-sized plant.