Hydrogen Generation, Storage, and Utilization

Topic Information

Dear Colleagues,

Hydrogen (H₂) is increasingly recognized as a clean and reliable energy vector for decarbonization in the future. It is an ideal fuel for substituting carbon-contained fossil entities because its consumption byproduct is only water, opening a promising possibility for green and renewable hydrogen energy economy. To realize this ambition, various research efforts have been made to explore low-cost and efficient engineering approaches for generating, storing, and utilizing hydrogen fuel sources. This research topic is favorable to publish the most recent findings and high-quality works, which focus on the hydrogen generation, storage, and utilization for the development of green and renewable hydrogen industries. The topic will cover but is not limited to:

• Hydrogen industries;
• Advanced hydrogen generation techniques;
• Efficient hydrogen storage methods;
• Hydrogen distribution and utilization;
• Fuel cell and hydrogen-contained systems: design, operation, and optimization;
• Novel hydrogen-based materials;
• Approaches and tools for modeling and optimization;
• Hydrogen leak detection and safety use;
• Energy harvesting and conversion;
• Hydrogen stationary and portable devices.

Prof. Dr. In-Hwan Lee
Prof. Dr. Duy Thanh Tran
Dr. Vandung Dao
Topic Editors

Keywords

Participating Journals

Journal Name	Impact Factor	CiteScore	Launched Year	First Decision (median)	APC
Catalysts catalysts	3.8	6.8	2011	13.9 Days	CHF 2200
Energies energies	3.0	6.2	2008	16.8 Days	CHF 2600
Hydrogen hydrogen	-	3.6	2020	14.8 Days	CHF 1000
Molecules molecules	4.2	7.4	1996	15.1 Days	CHF 2700
Nanomaterials nanomaterials	4.4	8.5	2010	14.1 Days	CHF 2400

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Published Papers (17 papers)

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14 pages, 3394 KiB  

Open AccessArticle

Impact of Depth on Underground Hydrogen Storage Operations in Deep Aquifers

by Katarzyna Luboń, Radosław Tarkowski and Barbara Uliasz-Misiak

Energies 2024, 17(6), 1268; https://doi.org/10.3390/en17061268 - 7 Mar 2024

Cited by 3 | Viewed by 2260

Abstract

Underground hydrogen storage in geological structures is considered appropriate for storing large amounts of hydrogen. Using the geological Konary structure in the deep saline aquifers, an analysis of the influence of depth on hydrogen storage was carried out. Hydrogen injection and withdrawal modeling [...] Read more.

Underground hydrogen storage in geological structures is considered appropriate for storing large amounts of hydrogen. Using the geological Konary structure in the deep saline aquifers, an analysis of the influence of depth on hydrogen storage was carried out. Hydrogen injection and withdrawal modeling was performed using TOUGH2 software, assuming different structure depths. Changes in the relevant parameters for the operation of an underground hydrogen storage facility, including the amount of H2 injected in the initial filling period, cushion gas, working gas, and average amount of extracted water, are presented. The results showed that increasing the depth to approximately 1500 m positively affects hydrogen storage (flow rate of injected hydrogen, total capacity, and working gas). Below this depth, the trend was reversed. The cushion gas-to-working gas ratio did not significantly change with increasing depth. Its magnitude depends on the length of the initial hydrogen filling period. An increase in the depth of hydrogen storage is associated with a greater amount of extracted water. Increasing the duration of the initial hydrogen filling period will reduce the water production but increase the cushion gas volume. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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17 pages, 7347 KiB  

Open AccessArticle

Enhanced Photoelectrochemical Performance Using Cobalt-Catalyst-Loaded PVD/RF-Engineered WO₃ Photoelectrodes

by Mansour Alhabradi, Xiuru Yang, Manal Alruwaili, Hong Chang and Asif Ali Tahir

Nanomaterials 2024, 14(3), 259; https://doi.org/10.3390/nano14030259 - 25 Jan 2024

Cited by 4 | Viewed by 1955

Abstract

Critical to boosting photoelectrochemical (PEC) performance is improving visible light absorption, accelerating carrier separation, and reducing electron–hole pair recombination. In this investigation, the PVD/RF method was employed to fabricate WO₃ thin films that were subsequently treated using the surface treatment process, and [...] Read more.

Critical to boosting photoelectrochemical (PEC) performance is improving visible light absorption, accelerating carrier separation, and reducing electron–hole pair recombination. In this investigation, the PVD/RF method was employed to fabricate WO₃ thin films that were subsequently treated using the surface treatment process, and the film surface was modified by introducing varying concentrations of cobalt nanoparticles, a non-noble metal, as an effective Co catalyst. The results show that the impact of loaded cobalt nanoparticles on the film surface can explain the extended absorption spectrum of visible light, efficiently capturing photogenerated electrons. This leads to an increased concentration of charge carriers, promoting a faster rate of carrier separation and enhancing interface charge transfer efficiency. Compared with a pristine WO₃ thin film photoanode, the photocurrent of the as-prepared Co/WO₃ films shows a higher PEC activity, with more than a one-fold increase in photocurrent density from 1.020 mA/cm² to 1.485 mA/cm² under simulated solar radiation. The phase, crystallinity, and surface of the prepared films were analysed using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. The PVD/RF method, scanning electron microscopy (FE-SEM), and high-resolution transmission electron microscopy (HR-TEM) were employed to assess the surface morphology of the fabricated film electrode. Optical properties were studied using UV–vis absorbance spectroscopy. Simultaneously, the photoelectrochemical properties of both films were evaluated using linear sweep voltammetry and electrochemical impedance spectroscopy (EIS). These results offer a valuable reference for designing high-performance photoanodes on a large scale for photoelectrochemical (PEC) applications. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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Supplementary material:
Supplementary File 1 (ZIP, 915 KiB)

22 pages, 5172 KiB  

Open AccessArticle

Optimization of an Open-Cell Foam-Based Ni-Mg-Al Catalyst for Enhanced CO₂ Hydrogenation to Methane

by Paulina Summa, Monika Motak and Patrick Da Costa

Catalysts 2024, 14(1), 11; https://doi.org/10.3390/catal14010011 - 21 Dec 2023

Cited by 1 | Viewed by 1705

Abstract

In the presented work, the catalytic performance of a nickel catalyst, in CO₂ hydrogenation to methane, within a ZrO₂ open-cell foam (OCF)-based catalyst was studied. Two series of analogous samples were prepared and coated with 100–150 mg of a Mg-Al oxide [...] Read more.

In the presented work, the catalytic performance of a nickel catalyst, in CO₂ hydrogenation to methane, within a ZrO₂ open-cell foam (OCF)-based catalyst was studied. Two series of analogous samples were prepared and coated with 100–150 mg of a Mg-Al oxide interface to stabilize the formation of well-dispersed Ni crystallites, with 10–15 wt% of nickel as an active phase, based on 30 ppi foam or 45 ppi foam. The main factor influencing catalytic performance was the geometric parameters of the applied foams. The series of catalysts based on 30 ppi OCF showed CO₂ conversion in the range of 30–50% at 300 °C, while those based on 45 ppi OCF resulted in a significantly enhancement of the catalytic activity: 90–92% CO₂ conversion under the same experimental conditions. Calculations of the internal and external mass transfer limitations were performed. The observed difference in the catalytic activity was primarily related to the radial transport inside the pores, confirmed with the explicitly higher conversions. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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14 pages, 3479 KiB  

Open AccessArticle

Ordered Mesoporous Carbons with Well-Dispersed Nickel or Platinum Nanoparticles for Room Temperature Hydrogen Adsorption

by Barbara Szczęśniak, Sylwia Głowniak, Jakub Woźniak, Stanisław Popiel, Jerzy Choma and Mietek Jaroniec

Molecules 2023, 28(18), 6551; https://doi.org/10.3390/molecules28186551 - 10 Sep 2023

Cited by 2 | Viewed by 1430

Abstract

A facile mechanochemical method was used for the synthesis of ordered mesoporous carbons (OMCs) with well-dispersed metal nanoparticles. The one-pot ball milling of tannins with a metal salt in the presence of a block copolymer followed by thermal treatment led to Ni- or [...] Read more.

A facile mechanochemical method was used for the synthesis of ordered mesoporous carbons (OMCs) with well-dispersed metal nanoparticles. The one-pot ball milling of tannins with a metal salt in the presence of a block copolymer followed by thermal treatment led to Ni- or Pt-embedded OMCs with high specific surface areas (up to 600 m²·g⁻¹) and large pore volumes (up to ~0.5 cm³·g⁻¹). The as-prepared OMC-based samples exhibited hexagonally ordered cylindrical mesopores with narrow pore size distributions (average pore size ~7 nm), which implies sufficient long-range copolymer-assisted self-assembly of the tannin-derived polymer upon milling even in the presence of a metal salt. The homogenous decoration of carbons with small-sized metal (Ni or Pt) particles was essential to provide H₂ storage capacities up to 0.33 wt.% at 25 °C and under 100 bar. The presented synthesis strategy seems to have great potential in the practical uses of functionalized polymers and carbons for applications in adsorption and catalysis. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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13 pages, 3781 KiB  

Open AccessArticle

Semi-Interpenetrating Network Anion Exchange Membranes by Thiol–Ene Coupling Reaction for Alkaline Fuel Cells and Water Electrolyzers

by Zhiyu Jin, Xiuyang Zou, Guodong Xu, Zhe Sun and Feng Yan

Molecules 2023, 28(14), 5470; https://doi.org/10.3390/molecules28145470 - 17 Jul 2023

Cited by 2 | Viewed by 1712

Abstract

In this work, a thiol–ene coupling reaction was employed to prepare the semi-interpenetrating polymer network AEMs. The obtained QP-1/2 membrane exhibits high hydroxide conductivity (162.5 mS cm⁻¹ at 80 °C) with a relatively lower swelling ratio, demonstrating its mechanical strength of 42 [...] Read more.

In this work, a thiol–ene coupling reaction was employed to prepare the semi-interpenetrating polymer network AEMs. The obtained QP-1/2 membrane exhibits high hydroxide conductivity (162.5 mS cm⁻¹ at 80 °C) with a relatively lower swelling ratio, demonstrating its mechanical strength of 42 MPa. This membrane is noteworthy for its improved alkaline stability, as the semi-interpenetrating network effectively limits the attack of hydroxide. Even after being treated in 2 M NaOH at 80 °C for 600 h, 82.5% of the hydroxide conductivity is maintained. The H₂/O₂ fuel cell with QP-1/2 membrane displays a peak power density of 521 mW cm⁻². Alkaline water electrolyzers based on QP-1/2 membrane demonstrated a current density of 1460 mA cm⁻² at a cell voltage of 2.00 V using NiCoFe catalysts in the anode. All the results demonstrate that a semi-interpenetrating structure is a promising way to enhance the mechanical property, ionic conductivity, and alkaline stability of AEMs for the application of alkaline fuel cells and water electrolyzers. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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10 pages, 1070 KiB  

Open AccessArticle

Device for Controlled Production of Hydrogen

by Alfonso Pozio

Hydrogen 2023, 4(3), 434-443; https://doi.org/10.3390/hydrogen4030029 - 15 Jul 2023

Viewed by 1910

Abstract

In this work, the production of hydrogen from the sodium borohydride (NaBH₄) reaction was studied using an experimental bench test in a passive device operating with or without minimal external energy input. The system consists of a reactor in which a [...] Read more.

In this work, the production of hydrogen from the sodium borohydride (NaBH₄) reaction was studied using an experimental bench test in a passive device operating with or without minimal external energy input. The system consists of a reactor in which a mixture based on sodium borohydride powders and an organic acid is confined. A flow of water feeds the area in which the solid mixture is confined, which undergoes a hydrolysis reaction and this generates gaseous hydrogen. The hydrogen thus produced, already saturated with water vapor, is particularly suitable for feeding polymer electrolyte fuel cells for the production of electricity because it does not require further humidification. The borohydride–organic acid coupling studied for this device, and its chemical process, provides high reaction and conversion kinetics, presenting remarkable chemical stability over time. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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15 pages, 3073 KiB  

Open AccessArticle

Geochemical Effects on Storage Gases and Reservoir Rock during Underground Hydrogen Storage: A Depleted North Sea Oil Reservoir Case Study

by Motaz Saeed, Prashant Jadhawar and Stefano Bagala

Hydrogen 2023, 4(2), 323-337; https://doi.org/10.3390/hydrogen4020023 - 18 May 2023

Cited by 41 | Viewed by 4718

Abstract

In this work, geochemical modelling using PhreeqC was carried out to evaluate the effects of geochemical reactions on the performance of underground hydrogen storage (UHS). Equilibrium, exchange, and mineral reactions were considered in the model. Moreover, reaction kinetics were considered to evaluate the [...] Read more.

In this work, geochemical modelling using PhreeqC was carried out to evaluate the effects of geochemical reactions on the performance of underground hydrogen storage (UHS). Equilibrium, exchange, and mineral reactions were considered in the model. Moreover, reaction kinetics were considered to evaluate the geochemical effect on underground hydrogen storage over an extended period of 30 years. The developed model was first validated against experimental data adopted from the published literature by comparing the modelling and literature values of H₂ and CO₂ solubility in water at varying conditions. Furthermore, the effects of pressure, temperature, salinity, and CO₂% on the H₂ and CO₂ inventory and rock properties in a typical sandstone reservoir were evaluated over 30 years. Results show that H₂ loss over 30 years is negligible (maximum 2%) through the studied range of conditions. The relative loss of CO₂ is much more pronounced compared to H₂ gas, with losses of up to 72%. Therefore, the role of CO₂ as a cushion gas will be affected by the CO₂ gas losses as time passes. Hence, remedial CO₂ gas injections should be considered to maintain the reservoir pressure throughout the injection and withdrawal processes. Moreover, the relative volume of CO₂ increases with the increase in temperature and decrease in pressure. Furthermore, the reservoir rock properties, porosity, and permeability, are affected by the underground hydrogen storage process and, more specifically, by the presence of CO₂ gas. CO₂ dissolves carbonate minerals inside the reservoir rock, causing an increase in the rock’s porosity and permeability. Consequently, the rock’s gas storage capacity and flow properties are enhanced. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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15 pages, 3661 KiB  

Open AccessArticle

Design and Scale-Up of Zero-Gap AEM Water Electrolysers for Hydrogen Production

by Adeline Loh, Xiaohong Li, Soraya Sluijter, Paige Shirvanian, Qingxue Lai and Yanyu Liang

Hydrogen 2023, 4(2), 257-271; https://doi.org/10.3390/hydrogen4020018 - 4 May 2023

Cited by 9 | Viewed by 9578

Abstract

The design of a 10 cm² (3.4 cm by 3.4 cm) and a 100 cm² (10 cm by 10 cm) anion exchange membrane (AEM) water electrolyser cell for hydrogen production are described. The AEM cells are based on a zero-gap configuration [...] Read more.

The design of a 10 cm² (3.4 cm by 3.4 cm) and a 100 cm² (10 cm by 10 cm) anion exchange membrane (AEM) water electrolyser cell for hydrogen production are described. The AEM cells are based on a zero-gap configuration where the AEM is sandwiched between the anode and cathode so as to minimise voltage drop between the electrodes. Nonprecious nickel-based metal alloy and metal oxide catalysts were employed. Various experiments were carried out to understand the effects of operating parameters such as current densities, electrolyte concentrations, and testing regimes on the performance of both 10 cm² and 100 cm² AEM electrolyser cells. Increasing electrolyte concentration was seen to result in reductions in overpotentials which were proportional to current applied, whilst the use of catalysts improved performance consistently over the range of current densities tested. Extended galvanostatic and intermittent tests were demonstrated on both 10 cm² and 100 cm² cells, with higher voltage efficiencies achieved with the use of electrocatalysts. Stability tests in the 100 cm² AEM electrolyser cell assembled with catalyst-coated electrodes demonstrated that the cell voltages remained stable at 2.03 V and 2.17 V during 72 h operation in 4 M KOH and 1 M KOH electrolyte, respectively, at a current density of 0.3 A cm⁻² at 323 K. The inclusion of cycling load tests in testing protocols is emphasized for rational evaluation of cell performance as this was observed to speed up the rate of degradation mechanisms such as membrane degradation. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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14 pages, 3012 KiB  

Open AccessArticle

New Process Combining Fe-Based Chemical Looping and Biomass Pyrolysis for Cogeneration of Hydrogen, Biochar, Bio-Oil and Electricity with In-Suit CO₂ Separation

by Xing Zhou, Huilong Jin, Na Li, Xiaolong Ma, Zichuan Ma, Pei Lu, Xiaomeng Yao and Shenna Chen

Molecules 2023, 28(6), 2793; https://doi.org/10.3390/molecules28062793 - 20 Mar 2023

Cited by 6 | Viewed by 2369

Abstract

Fe-based chemical looping gasification is a clean biomass technology, which has the advantage of reducing CO₂ emissions and the potential of self-sustaining operation without supplemental heating. A novel process combining Fe-based chemical looping and biomass pyrolysis was proposed and simulated using Aspen [...] Read more.

Fe-based chemical looping gasification is a clean biomass technology, which has the advantage of reducing CO₂ emissions and the potential of self-sustaining operation without supplemental heating. A novel process combining Fe-based chemical looping and biomass pyrolysis was proposed and simulated using Aspen Plus. The biomass was first subjected to pyrolysis to coproduce biochar, bio-oil and pyrolysis gas; the pyrolysis gas was subjected to an Fe looping process to obtain high-purity hydrogen and carbon dioxide. The influences of the pyrolysis reactor operating temperature and fuel reactor operation temperature, and the steam reactor and air reactor on the process performance are researched. The results showed that, under the operating condition of the established process, 23.07 kg/h of bio-oil, 24.18 kg/h of biochar, 3.35 kg/h of hydrogen and a net electricity of 3 kW can be generated from 100 kg/h of rice straw, and the outlet CO₂ concentration of the fuel reactor was as high as 80%. Moreover, the whole exergy efficiency and total exergy loss of the proposed process was 58.98% and 221 kW, respectively. Additionally, compared to biomass direct chemical looping hydrogen generation technology, the new process in this paper, using biomass pyrolysis gas as a reactant in the chemical looping hydrogen generation process, can enhance the efficiency of hydrogen generation. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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14 pages, 1071 KiB  

Open AccessArticle

An Ageing Test Standards Analysis on Thermoplastic Liners of Type IV Composite Hydrogen Storage Tanks

by Jun Li, Rongrong Lv, Chunlin Gu, Yitao Liu, Jiepu Li and Xiang Li

Energies 2023, 16(6), 2818; https://doi.org/10.3390/en16062818 - 17 Mar 2023

Cited by 6 | Viewed by 3631

Abstract

The liner of a carbon fiber fully reinforced composite tank with thermoplastic liner (type IV) works in a hydrogen environment with varying temperature and pressure profiles. The ageing performance of the thermoplastic liner may affect hydrogen permeability and the consequent storage capacity, degrade [...] Read more.

The liner of a carbon fiber fully reinforced composite tank with thermoplastic liner (type IV) works in a hydrogen environment with varying temperature and pressure profiles. The ageing performance of the thermoplastic liner may affect hydrogen permeability and the consequent storage capacity, degrade the mechanical properties, and even increase the leakage risks of type IV tanks. In this paper, both testing procedures and evaluation parameters of an ageing test in a hydrogen environment required in several standards are compared and analyzed. Hydrogen static exposure in a high-temperature condition with a constant temperature and pressure is suggested to be a reasonable way to accelerate the ageing reaction of thermoplastic materials. A total of 192 h is considered a superior ageing test duration to balance the test economy and safety. The ageing test temperature in the high-temperature condition is suggested as no lower than 85 °C, while the upper limit of test pressure is suggested to be 1.25 NWP. In addition, the hydrogen permeation coefficient and mechanical properties are recognized as important parameters in ageing performance evaluation. Considering the actual service conditions, the influence of temperature/pressure cycling, depressurization rate, and humidity on the ageing performance of thermoplastics in hydrogen are advised to be investigated experimentally. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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24 pages, 6030 KiB  

Open AccessReview

A Review on Numerical Simulation of Hydrogen Production from Ammonia Decomposition

by Rui Ao, Ruihua Lu, Guanghui Leng, Youran Zhu, Fuwu Yan and Qinghua Yu

Energies 2023, 16(2), 921; https://doi.org/10.3390/en16020921 - 13 Jan 2023

Cited by 19 | Viewed by 6232

Abstract

Ammonia (NH₃) is regarded as a promising medium of hydrogen storage, due to its large hydrogen storage density, decent performance on safety and moderate storage conditions. On the user side, NH₃ is generally required to decompose into hydrogen for utilization [...] Read more.

Ammonia (NH₃) is regarded as a promising medium of hydrogen storage, due to its large hydrogen storage density, decent performance on safety and moderate storage conditions. On the user side, NH₃ is generally required to decompose into hydrogen for utilization in fuel cells, and therefore it is vital for the NH₃-based hydrogen storage technology development to study NH₃ decomposition processes and improve the decomposition efficiency. Numerical simulation has become a powerful tool for analyzing the NH₃ decomposition processes since it can provide a revealing insight into the heat and mass transfer phenomena and substantial guidance on further improving the decomposition efficiency. This paper reviews the numerical simulations of NH₃ decomposition in various application scenarios, including NH₃ decomposition in microreactors, coupled combustion chemical reactors, solid oxide fuel cells, and membrane reactors. The models of NH₃ decomposition reactions in various scenarios and the heat and mass transport in the reactor are elaborated. The effects of reactor structure and operating conditions on the performance of NH₃ decomposition reactor are analyzed. It can be found that NH₃ decomposition in microchannel reactors is not limited by heat and mass transfer, and NH₃ conversion can be improved by using membrane reactors under the same conditions. Finally, research prospects and opportunities are proposed in terms of model development and reactor performance improvement for NH₃ decomposition. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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15 pages, 3955 KiB  

Open AccessArticle

Investigation of Hydrogen Production Performance Using Nanoporous NiCr and NiV Alloys in KBH₄ Hydrolysis

by Meryem Sena Akkus

Energies 2022, 15(24), 9547; https://doi.org/10.3390/en15249547 - 16 Dec 2022

Cited by 3 | Viewed by 2742

Abstract

Studies of storage and production of hydrogen, which is an alternative to fossil fuels, have been intensified. Hydrogen production from metal borohydrides via catalyst is very attractive because of its advantages, such as controlled production, high hydrogen content, nontoxicity, etc. In this study, [...] Read more.

Studies of storage and production of hydrogen, which is an alternative to fossil fuels, have been intensified. Hydrogen production from metal borohydrides via catalyst is very attractive because of its advantages, such as controlled production, high hydrogen content, nontoxicity, etc. In this study, the catalytic performances of nanoporous nickel–chromium alloy and nickel–vanadium alloy catalysts prepared with magnetron sputtering in hydrolysis of potassium borohydride, which is a hydrogen storage material, were investigated. Parameters that affected the hydrolysis reaction rate, such as the temperature, the amount of catalyst, and the volume of 0.5 M HCl solution were investigated using response surface methodology. In addition, the prepared catalysts were characterized with XRD and FE-SEM analysis, and the remaining solutions after the reactions were characterized with FE-SEM/EDS analysis. Using response surface methodology, optimum conditions for the maximum hydrogen production rate were determined to be 1.65 g of catalyst, 6% KBH₄, 3% NaOH, and 7 mL of 0.5 M HCl at 333 K. Under these conditions, the hydrogen production rates were calculated as 68.9 L·min⁻¹·g_cat⁻¹ and 76.5 L·min⁻¹·g_cat⁻¹ for NiCr and NiV, respectively. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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23 pages, 4911 KiB  

Open AccessArticle

Refurbishment of Natural Gas Pipelines towards 100% Hydrogen—A Thermodynamic-Based Analysis

by Nejc Klopčič, Thomas Stöhr, Ilena Grimmer, Markus Sartory and Alexander Trattner

Energies 2022, 15(24), 9370; https://doi.org/10.3390/en15249370 - 10 Dec 2022

Cited by 19 | Viewed by 3977

Abstract

Hydrogen is a key enabler of a sustainable society. Refurbishment of the existing natural gas infrastructure for up to 100% H₂ is considered one of the most energy- and resource-efficient energy transportation methods. The question remains whether the transportation of 100% H [...] Read more.

Hydrogen is a key enabler of a sustainable society. Refurbishment of the existing natural gas infrastructure for up to 100% H₂ is considered one of the most energy- and resource-efficient energy transportation methods. The question remains whether the transportation of 100% H₂ with reasonable adaptions of the infrastructure and comparable energy amounts to natural gas is possible. The well-known critical components for refurbishment, such as increased compressor power, reduced linepack as well as pipeline transport efficiencies, and their influencing factors were considered based on thermodynamic calculations with a step-by-step overview. A H₂ content of 20–30% results in comparable operation parameters to pure natural gas. In addition to transport in pipelines, decentralized H₂ production will also play an important role in addressing future demands. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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17 pages, 3514 KiB  

Open AccessArticle

Experimental and Numerical Research on Temperature Evolution during the Fast-Filling Process of a Type III Hydrogen Tank

by Bin Zhao, Huan Wei, Xueyuan Peng, Jianmei Feng and Xiaohan Jia

Energies 2022, 15(10), 3811; https://doi.org/10.3390/en15103811 - 22 May 2022

Cited by 11 | Viewed by 2382

Abstract

The temperature rises hydrogen tanks during the fast-filling process could threaten the safety of the hydrogen fuel cell vehicle. In this paper, a 2D axisymmetric model of a type III hydrogen for the bus was built to investigate the temperature evolution during the [...] Read more.

The temperature rises hydrogen tanks during the fast-filling process could threaten the safety of the hydrogen fuel cell vehicle. In this paper, a 2D axisymmetric model of a type III hydrogen for the bus was built to investigate the temperature evolution during the fast-filling process. A test rig was carried out to validate the numerical model with air. It was found significant temperature rise occurred during the filling process, despite the temperature of the filling air being cooled down due to the throttling effect. After verification, the 2D model of the hydrogen tank was employed to study the temperature distribution and evolution of hydrogen during the fast-filling process. Thermal stratification was observed along the axial direction of the tank. Then, the effects of filling parameters were examined, and a formula was fitted to predict the final temperature based on the simulated results. At last, an effort was paid on trying the improve the temperature distribution by increasing the injector length of the hydrogen tank. The results showed the maximal temperature and mass averaged temperature decreased by 2 K and 3.4 K with the length of the injector increased from 50 mm to 250 mm. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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32 pages, 2349 KiB  

Open AccessReview

Hydrogen Blending in Gas Pipeline Networks—A Review

by Devinder Mahajan, Kun Tan, T. Venkatesh, Pradheep Kileti and Clive R. Clayton

Energies 2022, 15(10), 3582; https://doi.org/10.3390/en15103582 - 13 May 2022

Cited by 139 | Viewed by 21884

Abstract

Replacing fossil fuels with non-carbon fuels is an important step towards reaching the ultimate goal of carbon neutrality. Instead of moving directly from the current natural gas energy systems to pure hydrogen, an incremental blending of hydrogen with natural gas could provide a [...] Read more.

Replacing fossil fuels with non-carbon fuels is an important step towards reaching the ultimate goal of carbon neutrality. Instead of moving directly from the current natural gas energy systems to pure hydrogen, an incremental blending of hydrogen with natural gas could provide a seamless transition and minimize disruptions in power and heating source distribution to the public. Academic institutions, industry, and governments globally, are supporting research, development and deployment of hydrogen blending projects such as HyDeploy, GRHYD, THyGA, HyBlend, and others which are all seeking to develop efficient pathways to meet the carbon reduction goal in coming decades. There is an understanding that successful commercialization of hydrogen blending requires both scientific advances and favorable techno-economic analysis. Ongoing studies are focused on understanding how the properties of methane-hydrogen mixtures such as density, viscosity, phase interactions, and energy densities impact large-scale transportation via pipeline networks and end-use applications such as in modified engines, oven burners, boilers, stoves, and fuel cells. The advantages of hydrogen as a non-carbon energy carrier need to be balanced with safety concerns of blended gas during transport, such as overpressure and leakage in pipelines. While studies on the short-term hydrogen embrittlement effect have shown essentially no degradation in the metal tensile strength of pipelines, the long-term hydrogen embrittlement effect on pipelines is still the focus of research in other studies. Furthermore, pressure reduction is one of the drawbacks that hydrogen blending brings to the cost dynamics of blended gas transport. Hence, techno-economic models are also being developed to understand the energy transportation efficiency and to estimate the true cost of delivery of hydrogen blended natural gas as we move to decarbonize our energy systems. This review captures key large-scale efforts around the world that are designed to increase the confidence for a global transition to methane-hydrogen gas blends as a precursor to the adoption of a hydrogen economy by 2050. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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18 pages, 3775 KiB  

Open AccessCommunication

Microbial Biogas Production from Pork Gelatine

by Gaweł Sołowski

Hydrogen 2022, 3(2), 179-196; https://doi.org/10.3390/hydrogen3020012 - 6 May 2022

Cited by 3 | Viewed by 2636

Abstract

This research describes the results of the anaerobic digestion of gelatine as a potential hydrogen source with heat-shocked inoculum. The concentrations of applied gelatine were of VSS (volatile suspended solids) ranging from 10 g VSS/L to 30 g VSS/L. The initial process pH [...] Read more.

This research describes the results of the anaerobic digestion of gelatine as a potential hydrogen source with heat-shocked inoculum. The concentrations of applied gelatine were of VSS (volatile suspended solids) ranging from 10 g VSS/L to 30 g VSS/L. The initial process pH was 5.5, and, depending on the concentration, reached pH values from 7.5 to 7.8 after 55 days. Although the inoculum was heat-shocked in 30 g VSS/L of collagen, the process that occurred was hydrogenotrophic anaerobic digestion. In gelatine concentrations below 30 g VSS/L, hydrogen production was dominant only during the first 5 days of the experiments. Then, there was a change from dark fermentation to hydrogenotrophic methane production. The optimal hydrogen and methane yields resulted from the concentrations of 10 g VSS/L (7.65 mL ± 0.01 mL H₂/g VSS and 3.49 ± 0.01 L CH₄/g VSS). Additionally, 10 g VSS/L had the lowest accumulated emission of hydrogen sulphide (10.3 ± 0.01 mL of H₂S), while 30 g VSS/L (0.440 ± 0.01mL H₂S/g VSS) produced the lowest yield. After a lag time, the hydrogen production and hydrogen sulphide grew with a specific ratio, depending on the concentration. The hydrogen sulphide emission and sulphur added analysis proved that hydrogen sulphide originating from biogas created by bacteria remains longer than that from a substrate. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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11 pages, 3378 KiB  

Open AccessArticle

Insight into the Growth Mechanism of Mixed Phase CZTS and the Photocatalytic Performance

by Ying Yang, Yaya Ding, Jingyu Zhang, Nina Liang, Lizhen Long and Jun Liu

Nanomaterials 2022, 12(9), 1439; https://doi.org/10.3390/nano12091439 - 23 Apr 2022

Cited by 16 | Viewed by 2198

Abstract

In this work, CZTS particles with a mixed phase of wurtzite and kesterite were synthesized by the solvothermal method. The time-dependent XRD patterns, Raman spectra, SEM, and EDS analysis were employed to study the growth mechanism of CZTS. The results revealed that the [...] Read more.

In this work, CZTS particles with a mixed phase of wurtzite and kesterite were synthesized by the solvothermal method. The time-dependent XRD patterns, Raman spectra, SEM, and EDS analysis were employed to study the growth mechanism of CZTS. The results revealed that the formation of CZTS started from the nucleation of monoclinic Cu₇S₄ seeds, followed by the successive incorporation of Zn²⁺ and Sn⁴⁺ ions. Additionally, the diffusion of Zn²⁺ into Cu₇S₄ crystal lattice is much faster than that of Sn⁴⁺. With increasing time, CZTS undergoes a phase transformation from metastable wurtzite to steady kesterite. The morphology of CZTS tends to change from spherical-like to flower-like architecture. The mixed-phase CZTS with a bandgap of 1.5 eV exhibited strong visible light absorption, good capability for photoelectric conversion, and suitable band alignment, which makes it capable to produce H₂ production and degrade RhB under simulated solar illumination. Full article

(This article belongs to the Topic Hydrogen Generation, Storage, and Utilization)

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