Large hydrate reservoirs in the Arctic regions could provide great potentials for recovery of methane and geological storage of CO. In this study, injection of flue gas into permafrost gas hydrates reservoirs has been studied in order to evaluate its use in energy recovery and CO sequestration based on the premise that it could significantly lower costs relative to other technologies available today. We have carried out a series of real-time scale experiments under realistic conditions at temperatures between 261.2 and 284.2 K and at optimum pressures defined in our previous work, in order to characterize the kinetics of the process and evaluate efficiency. Results show that the kinetics of methane release from methane hydrate and CO extracted from flue gas strongly depend on hydrate reservoir temperatures. The experiment at 261.2 K yielded a capture of 81.9% CO present in the injected flue gas, and an increase in the CH concentration in the gas phase up to 60.7 mol%, 93.3 mol%, and 98.2 mol% at optimum pressures, after depressurizing the system to dissociate CH hydrate and after depressurizing the system to CO hydrate dissociation point, respectively. This is significantly better than the maximum efficiency reported in the literature for both CO sequestration and methane recovery using flue gas injection, demonstrating the economic feasibility of direct injection flue gas into hydrate reservoirs in permafrost for methane recovery and geological capture and storage of CO. Finally, the thermal stability of stored CO was investigated by heating the system and it is concluded that presence of N in the injection gas provides another safety factor for the stored CO in case of temperature change.
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http://dx.doi.org/10.1038/s41598-019-52745-x | DOI Listing |
iScience
August 2024
Ocean College, Zhejiang University, Zhoushan, Zhejiang 316021, China.
A major obstacle to exploiting industrial flue gas for microalgae cultivation is the unfavorable acidic environment. We previously identified three upregulated genes in the low-pH-adapted model diatom : ferredoxin (PtFDX), cation/proton antiporter (PtCPA), and HCO transporter (PtSCL4-2). Here, we individually overexpressed these genes in to investigate their respective roles in resisting acidic stress (pH 5.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Key Laboratory of Groundwater Resources and Environment (Jilin University), Ministry of Education, College of New Energy and Environment, Jilin University, Changchun 130021, China. Electronic address:
As the frontier of environmental catalysis, mercury removal by deNO unit over bifunctional catalyst has emerged. However, it is fundamentally challenging to achieve simultaneous NO and mercury removal in industrial flue gas due to the commercial selective catalytic reduction (SCR) molecular sieves' lack of demercuration active centers. Herein, we demonstrate an active site in situ reconfiguration approach to enhance the oxidation of elemental mercury and immobilize divalent mercury by modified commercial SCR catalysts.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Materials Science and Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919 Republic of Korea.
The simultaneous removal reaction (SRR) is a pioneering approach for achieving the simultaneous removal of anthropogenic NO and CO pollutants through catalytic reactions. To facilitate this removal across diverse industrial fields, it is crucial to understand the trade-offs and synergies among the multiple reactions involved in the SRR process. In this study, we developed mixed metal oxide nanostructures derived from layered double hydroxides as catalysts for the SRR, achieving high catalytic conversions of 93.
View Article and Find Full Text PDFJ Environ Manage
December 2024
Key Laboratory of Energy Thermal Conversion and Control, Ministry of Education, School of Energy and Environment, Southeast University, Nanjing, 210096, PR China.
J Colloid Interface Sci
December 2024
College of Materials Science and Engineering, Xi'an University of Architecture and Technology, Xi'an 710055, PR China. Electronic address:
NH-MIL-125 with abundant porosity and specific interactions with CO molecules, has been demonstrate great potential in the field of photocatalytic CO reduction. However, conventional NH-MIL-125 and their composites much lower CO photoreduction efficiency in aerobic environments because of the O competition. To circumvent the issue, this study modifies NH-MIL-125 through crystal facet engineering to enhance its selective CO adsorption and photocatalytic efficiency in the environment of impurity CO.
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