Jyoti Shanker Pandey
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Jyoti Shanker Pandey has a total of 64 co-authors. Here are the top co-authors by number of shared publications:
- Nicolas von Solms
Center for Energy Resources Engineering, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, Kongens Lyngby 2800, Denmark
21 shared publications - Adam Paul Karcz
Department of Materials Science and Engineering, University of Maryland, College Park, MD 20742 (USA)
4 shared publications Qian Ouyang
4 shared publicationsGeir Ersland
Department of Physics and Technology, University of Bergen, 5007 Bergen, Norway
3 shared publications- Shanker Krishna
Department of Petroleum Engineering, School of Energy Technology, Pandit Deendayal Energy University, Knowledge Hub, Raysan, Gandhinagar 382426, Gujarat, India
3 shared publications - Stian Almenningen
Department of Physics and Technology, University of Bergen, 5007 Bergen, Norway
3 shared publications
Latest Publications
- Open Access
- 7 August 2026
- Published by Elsevier in Journal of Environmental Chemical Engineering
- Vol. 14 (5)
Aqueous remediation of pharmaceutical and personal care pollutants: Comparative insights into MIL and Zr MOF systems and future trends
- 7 August 2026
- Published by Elsevier in Journal of Environmental Chemical Engineering
- Vol. 14 (5)
Open AccessAqueous remediation of pharmaceutical and personal care pollutants: Comparative insights into MIL and Zr MOF systems and future trends
- Open Access
- 27 July 2026
- Published by Elsevier in Journal of Environmental Chemical Engineering
- Vol. 14 (6)
Review of clathrate hydrate-based CO2 capture: Benchmarking performance, economics, and life cycle considerations
- 27 July 2026
- Published by Elsevier in Journal of Environmental Chemical Engineering
- Vol. 14 (6)
Open AccessReview of clathrate hydrate-based CO2 capture: Benchmarking performance, economics, and life cycle considerations
- Open Access
- 17 February 2026
- Published by Elsevier in Trends in Food Science & Technology
- Vol. 171
Atomic force microscopy in food industry: Bridging nanoscale analysis and real-world applications
- 17 February 2026
- Published by Elsevier in Trends in Food Science & Technology
- Vol. 171
Open AccessAtomic force microscopy in food industry: Bridging nanoscale analysis and real-world applications
- 10 October 2025
- Published by American Chemical Society (ACS) in Energy & Fuels
- Vol. 39 (42) , 19998-20055
Advances in Spectroscopic Methods for Gas Hydrate: A Review and Perspectives for Low-Carbon Energy Solutions and Applications
- 10 October 2025
- Published by American Chemical Society (ACS) in Energy & Fuels
- Vol. 39 (42) , 19998-20055
Advances in Spectroscopic Methods for Gas Hydrate: A Review and Perspectives for Low-Carbon Energy Solutions and Applications
- 3 March 2025
- Published by Elsevier in Coordination Chemistry Reviews
- Vol. 534, 216552
Exploring cellular dynamics: Engineered fluorescent carbon dots for organelle staining and cellular response analysis
- 3 March 2025
- Published by Elsevier in Coordination Chemistry Reviews
- Vol. 534, 216552
Exploring cellular dynamics: Engineered fluorescent carbon dots for organelle staining and cellular response analysis
- 6 December 2024
- Published by American Chemical Society (ACS) in Energy & Fuels
- Vol. 38 (24) , 23192-23229
The Role of Gas Hydrates in Storing Natural Gas-Hydrogen Blends for Coupling Power-to-X and Decarbonization
- 6 December 2024
- Published by American Chemical Society (ACS) in Energy & Fuels
- Vol. 38 (24) , 23192-23229
The Role of Gas Hydrates in Storing Natural Gas-Hydrogen Blends for Coupling Power-to-X and Decarbonization
- 25 November 2024
- Published by American Chemical Society (ACS) in Energy & Fuels
- Vol. 38 (23) , 22926-22946
CO2 Hydrate Formation Kinetics Using Aqueous MOF Ink-Soaked Water-Absorbing Materials
- 25 November 2024
- Published by American Chemical Society (ACS) in Energy & Fuels
- Vol. 38 (23) , 22926-22946
CO2 Hydrate Formation Kinetics Using Aqueous MOF Ink-Soaked Water-Absorbing Materials
- Open Access
CH4 Adsorption in Wet Metal-Organic Frameworks under Gas Hydrate Formation Conditions Using A Large Reactor
Nanoporous materials, such as metal-organic frameworks (MOFs), are renowned for their high selectivity as gas adsorbents due to their specific surface area, nanoporosity, and active surface chemistry. A significant challenge for their widespread application is reduced gas uptake in wet conditions, attributed to competitive adsorption between gas and water. Recent studies of gas adsorption in wet materials have typically used small amounts of powdered porous materials (in the milligram range) within very small reactors (1–5 mL). This leaves a gap in knowledge about gas adsorption behaviors in larger reactors and with increased MOF sample sizes (to the gram scale). Additionally, there has been a notable absence of experimental research on MOFs heavily saturated with water. In this study, we aimed to fill the gaps in our understanding of gas adsorption in wet conditions by measuring CH4 adsorption in MOFs. To do this, we used larger MOF samples (in grams) and a large-volume reactor. Our selection of commercially available MOFs, including HKUST-1, ZIF-8, MOF-303, and activated carbon, was based on their widespread application, available previous research, and differences in hydrophobicity. Using a volumetric approach, we measured high-pressure isotherms (at T = 274.15 K) to compare the moles of gas adsorbed under both dry and wet conditions across different MOFs and weights. The experimental results indicate that water decreases total CH4 adsorption in MOFs, with a more pronounced decrease in hydrophilic MOFs compared to hydrophobic ones at lower pressures. However, hydrophilic MOFs exhibited stepped isotherms at higher pressures, suggesting water converts to hydrate, positively impacting total gas uptake. In contrast, the hydrophobic ZIF-8 did not promote hydrate formation due to particle aggregation in the presence of water, leading to a loss of surface area and surface charge. This study highlights the additional challenges associated with hydrate-MOF synergy when experiments are scaled up and larger sample sizes are used. Future studies should consider using monolith or pellet forms of MOFs to address the limitations of powdered MOFs in scale-up studies.
Open AccessCH4 Adsorption in Wet Metal-Organic Frameworks under Gas Hydrate Formation Conditions Using A Large Reactor
Nanoporous materials, such as metal-organic frameworks (MOFs), are renowned for their high selectivity as gas adsorbents due to their specific surface area, nanoporosity, and active surface chemistry. A significant challenge for their widespread application is reduced gas uptake in wet conditions, attributed to competitive adsorption between gas and water. Recent studies of gas adsorption in wet materials have typically used small amounts of powdered porous materials (in the milligram range) within very small reactors (1–5 mL). This leaves a gap in knowledge about gas adsorption behaviors in larger reactors and with increased MOF sample sizes (to the gram scale). Additionally, there has been a notable absence of experimental research on MOFs heavily saturated with water. In this study, we aimed to fill the gaps in our understanding of gas adsorption in wet conditions by measuring CH4 adsorption in MOFs. To do this, we used larger MOF samples (in grams) and a large-volume reactor. Our selection of commercially available MOFs, including HKUST-1, ZIF-8, MOF-303, and activated carbon, was based on their widespread application, available previous research, and differences in hydrophobicity. Using a volumetric approach, we measured high-pressure isotherms (at T = 274.15 K) to compare the moles of gas adsorbed under both dry and wet conditions across different MOFs and weights. The experimental results indicate that water decreases total CH4 adsorption in MOFs, with a more pronounced decrease in hydrophilic MOFs compared to hydrophobic ones at lower pressures. However, hydrophilic MOFs exhibited stepped isotherms at higher pressures, suggesting water converts to hydrate, positively impacting total gas uptake. In contrast, the hydrophobic ZIF-8 did not promote hydrate formation due to particle aggregation in the presence of water, leading to a loss of surface area and surface charge. This study highlights the additional challenges associated with hydrate-MOF synergy when experiments are scaled up and larger sample sizes are used. Future studies should consider using monolith or pellet forms of MOFs to address the limitations of powdered MOFs in scale-up studies.
- Open Access
- 13 July 2024
- Published by Elsevier in Renewable and Sustainable Energy Reviews
- Vol. 203
Fundamental insights into multistep depressurization of CH4/CO2 hydrates in the presence of N2 or air
- 13 July 2024
- Published by Elsevier in Renewable and Sustainable Energy Reviews
- Vol. 203
Open AccessFundamental insights into multistep depressurization of CH4/CO2 hydrates in the presence of N2 or air