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CO2 Capture, Storage, Utilisation and Sequestration and Hydrocarbon Extraction

A special issue of Energies (ISSN 1996-1073). This special issue belongs to the section "H: Geo-Energy".

Deadline for manuscript submissions: closed (20 November 2021) | Viewed by 7616

Special Issue Editors


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Guest Editor
Department of Chemical Engineering, University of Western Australia, 35 Stirling Highway, Crawley 6009, Australia
Interests: gas hydrates; CO2 capture and storage; CO2 separation and sequestration; natural gas storage; methane recovery; flow assurance; hydrate-based water treatment; hydrogen storage

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Guest Editor
Department of Chemical Engineering, Indian Institute of Technology, Roorkee, India
Interests: gas hydrates; energy storage; energy recovery; gas separation/enrichment; carbon dioxide capture and sequestration; water treatment/Desalination; flue gas desulphurization and integrated gasification combined cycle (IGCC)

Special Issue Information

Dear Colleagues,

Submissions are invited to a Special Issue of the Energies journal on the topic of “CO2 Capture, Utilisation, Storage/Sequestration and Hydrocarbon Recovery”. CO2 is a major greenhouse gas, and its alarming increase in recent times poses a severe threat to the environment and contributes significantly to the global climate change. Plausible strategies for meeting the set CO2 emission reduction targets include carbon dioxide capture and storage(CCS) along with its utilisation and sequestration. Further, CO2 can also be used to enhance hydrocarbon recovery, and after the depletion of hydrocarbons in the reservoirs, CO2 could be stored in them. Recently, CO2 has been employed to replace methane trapped in natural hydrate deposits. This promising approach paves the way to secure the future energy (methane/natural gas) necessities and simultaneously alleviates CO2 emissions.

This Special Issue aims to publish original research and review articles focusing on salient aspects of CO2 capture, storage, utilisation and sequestration, including but not limited to existing/novel materials, potential technologies and associated process development. Substitution of CO2 with methane from hydrate deposits for enhanced methane recovery coupled with CO2 capture/sequestration is also considered. Further, this issue is also open for emerging hydrocarbon extraction techniques utilising CO2 to enhance the efficiency, versatility, yield and safety of the hydrocarbon recovery process.

Dr. Asheesh Kumar
Dr. Hari Prakash Veluswamy
Guest Editors

Manuscript Submission Information

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Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Energies is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • CO2 capture and storage materials
  • CO2 utilisation and sequestration processes
  • Hydrate-based carbon capture technologies
  • Hydrocarbon recovery using CO2
  • Methane-CO2 replacement process in hydrates

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Published Papers (2 papers)

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Research

28 pages, 4903 KiB  
Article
Enhanced Hydrate-Based Geological CO2 Capture and Sequestration as a Mitigation Strategy to Address Climate Change
by Jyoti Shanker Pandey, Yousef Jouljamal Daas, Adam Paul Karcz and Nicolas von Solms
Energies 2020, 13(21), 5661; https://doi.org/10.3390/en13215661 - 29 Oct 2020
Cited by 19 | Viewed by 3349
Abstract
Geological sequestration of CO2-rich gas as a CO2 capture and storage technique has a lower technical and cost barrier compared to industrial scale-up. In this study, we have proposed CO2 capture and storage via hydrate in geological formation within [...] Read more.
Geological sequestration of CO2-rich gas as a CO2 capture and storage technique has a lower technical and cost barrier compared to industrial scale-up. In this study, we have proposed CO2 capture and storage via hydrate in geological formation within the hydrate stability zone as a novel technique to contribute to global warming mitigation strategies, including carbon capture, utilization, and storage (CCUS) and to prevent vast methane release into the atmosphere caused by hydrate melting. We have attempted to enhance total gas uptake and CO2 capture efficiency in hydrate in the presence of kinetic promoters while using diluted CO2 gas (CO2-N2 mixture). Experiments are performed using unfrozen sands within hydrate stability zone condition and in the presence of low dosage surfactant and amino acids. Hydrate formation parameters, including sub-cooling temperature, induction time, total gas uptake, and split fraction, are calculated during the single-step formation and dissociation process. The effect of sands with varying particle sizes (160–630 µm, 1400–5000 µm), low dosage promoter (500–3000 ppm) and CO2 concentration in feed gas (20–30 mol%) on formation kinetic parameters was investigated. Enhanced formation kinetics are observed in the presence of surfactant (1000–3000 ppm) and hydrophobic amino acids (3000 ppm) at 120 bar and 1 ℃ experimental conditions. We report induction time in the range of 7–170 min and CO2 split fraction (0.60–0.90) in hydrate for 120 bar initial injection pressure. CO2 split fraction can be enhanced by reducing sand particle size or increasing the CO2 mol% in incoming feed gas at given injection pressure. This study also reports that formation kinetics in a porous medium are influenced by hydrate morphology. Hydrate morphology influences gas and water migration within sediments and controls pore space or particle surface correlation with the formation kinetics within coarse sediments. This investigation demonstrates the potential application of bio-friendly amino acids as promoters to enhance CO2 capture and storage within hydrate. Sufficient contact time at gas-liquid interface and higher CO2 separation efficiency is recorded in the presence of amino acids. The findings of this study could be useful in exploring the promoter-driven pore habitat of CO2-rich hydrates in sediments to address climate change. Full article
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30 pages, 6581 KiB  
Article
Enhanced CH4-CO2 Hydrate Swapping in the Presence of Low Dosage Methanol
by Jyoti Shanker Pandey, Charilaos Karantonidis, Adam Paul Karcz and Nicolas von Solms
Energies 2020, 13(20), 5238; https://doi.org/10.3390/en13205238 - 9 Oct 2020
Cited by 27 | Viewed by 3311
Abstract
CO2-rich gas injection into natural gas hydrate reservoirs is proposed as a carbon-neutral, novel technique to store CO2 while simultaneously producing CH4 gas from methane hydrate deposits without disturbing geological settings. This method is limited by the mass transport [...] Read more.
CO2-rich gas injection into natural gas hydrate reservoirs is proposed as a carbon-neutral, novel technique to store CO2 while simultaneously producing CH4 gas from methane hydrate deposits without disturbing geological settings. This method is limited by the mass transport barrier created by hydrate film formation at the liquid–gas interface. The very low gas diffusivity through hydrate film formed at this interface causes low CO2 availability at the gas–hydrate interface, thus lowering the recovery and replacement efficiency during CH4-CO2 exchange. In a first-of-its-kind study, we have demonstrate the successful application of low dosage methanol to enhance gas storage and recovery and compare it with water and other surface-active kinetic promoters including SDS and L-methionine. Our study shows 40–80% CH4 recovery, 83–93% CO2 storage and 3–10% CH4-CO2 replacement efficiency in the presence of 5 wt% methanol, and further improvement in the swapping process due to a change in temperature from 1–4 °C is observed. We also discuss the influence of initial water saturation (30–66%), hydrate morphology (grain-coating and pore-filling) and hydrate surface area on the CH4-CO2 hydrate swapping. Very distinctive behavior in methane recovery caused by initial water saturation (above and below Swi = 0.35) and hydrate morphology is also discussed. Improved CO2 storage and methane recovery in the presence of methanol is attributed to its dual role as anti-agglomerate and thermodynamic driving force enhancer between CH4-CO2 hydrate phase boundaries when methanol is used at a low concentration (5 wt%). The findings of this study can be useful in exploring the usage of low dosage, bio-friendly, anti-agglomerate and hydrate inhibition compounds in improving CH4 recovery and storing CO2 in hydrate reservoirs without disturbing geological formation. To the best of the authors’ knowledge, this is the first experimental study to explore the novel application of an anti-agglomerate and hydrate inhibitor in low dosage to address the CO2 hydrate mass transfer barrier created at the gas–liquid interface to enhance CH4-CO2 hydrate exchange. Our study also highlights the importance of prior information about methane hydrate reservoirs, such as residual water saturation, degree of hydrate saturation and hydrate morphology, before applying the CH4-CO2 hydrate swapping technique. Full article
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