Antifreezes act as catalysts for methane hydrate formation from ice

Contrary to the thermodynamic inhibiting effect of methanol on methane hydrate formation from aqueous phases, hydrate forms quickly at high yield by exposing frozen water-methanol mixtures with methanol concentrations ranging from 0.6-10 wt% to methane gas at pressures from 125 bars at 253 K. Format...

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Published in:Angewandte Chemie International Edition
Main Authors: McLaurin, Graham, Shin, Kyuchul, Alavi, Saman, Ripmeester, John A.
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2014
Subjects:
Online Access:https://doi.org/10.1002/anie.201403638
https://nrc-publications.canada.ca/eng/view/object/?id=946fcd26-4c59-4998-b55d-0413c180e5d5
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spelling ftnrccanada:oai:cisti-icist.nrc-cnrc.ca:cistinparc:21272664 2023-05-15T17:11:32+02:00 Antifreezes act as catalysts for methane hydrate formation from ice McLaurin, Graham Shin, Kyuchul Alavi, Saman Ripmeester, John A. 2014-09-24 text https://doi.org/10.1002/anie.201403638 https://nrc-publications.canada.ca/eng/view/object/?id=946fcd26-4c59-4998-b55d-0413c180e5d5 https://nrc-publications.canada.ca/fra/voir/objet/?id=946fcd26-4c59-4998-b55d-0413c180e5d5 eng eng Wiley issn:1433-7851 Angewandte Chemie - International Edition, Volume: 53, Issue: 39, Publication date: 2014-09-24, Pages: 10429–10433 doi:10.1002/anie.201403638 Methanol Molecular dynamics Gas uptake Methane hydrates Powder X ray diffraction Hydrates article 2014 ftnrccanada https://doi.org/10.1002/anie.201403638 2021-09-01T06:28:12Z Contrary to the thermodynamic inhibiting effect of methanol on methane hydrate formation from aqueous phases, hydrate forms quickly at high yield by exposing frozen water-methanol mixtures with methanol concentrations ranging from 0.6-10 wt% to methane gas at pressures from 125 bars at 253 K. Formation rates are some two orders of magnitude greater than those obtained for samples without methanol and conversion of ice is essentially complete. Ammonia has a similar catalytic effect when used in concentrations of 0.3-2.7 wt%. The structure I methane hydrate formed in this manner was characterized by powder X-ray diffraction and Raman spectroscopy. Steps in the possible mechanism of action of methanol were studied with molecular dynamics simulations of the Ih (0001) basal plane exposed to methanol and methane gas. Simulations show that methanol from a surface aqueous layer slowly migrates into the ice lattice. Methane gas is preferentially adsorbed into the aqueous methanol surface layer. Possible consequences of the catalytic methane hydrate formation on hydrate plug formation in gas pipelines, on large scale energy-efficient gas hydrate formation, and in planetary science are discussed. Peer reviewed: Yes NRC publication: Yes Article in Journal/Newspaper Methane hydrate National Research Council Canada: NRC Publications Archive Angewandte Chemie International Edition 53 39 10429 10433
institution Open Polar
collection National Research Council Canada: NRC Publications Archive
op_collection_id ftnrccanada
language English
topic Methanol
Molecular dynamics
Gas uptake
Methane hydrates
Powder X ray diffraction
Hydrates
spellingShingle Methanol
Molecular dynamics
Gas uptake
Methane hydrates
Powder X ray diffraction
Hydrates
McLaurin, Graham
Shin, Kyuchul
Alavi, Saman
Ripmeester, John A.
Antifreezes act as catalysts for methane hydrate formation from ice
topic_facet Methanol
Molecular dynamics
Gas uptake
Methane hydrates
Powder X ray diffraction
Hydrates
description Contrary to the thermodynamic inhibiting effect of methanol on methane hydrate formation from aqueous phases, hydrate forms quickly at high yield by exposing frozen water-methanol mixtures with methanol concentrations ranging from 0.6-10 wt% to methane gas at pressures from 125 bars at 253 K. Formation rates are some two orders of magnitude greater than those obtained for samples without methanol and conversion of ice is essentially complete. Ammonia has a similar catalytic effect when used in concentrations of 0.3-2.7 wt%. The structure I methane hydrate formed in this manner was characterized by powder X-ray diffraction and Raman spectroscopy. Steps in the possible mechanism of action of methanol were studied with molecular dynamics simulations of the Ih (0001) basal plane exposed to methanol and methane gas. Simulations show that methanol from a surface aqueous layer slowly migrates into the ice lattice. Methane gas is preferentially adsorbed into the aqueous methanol surface layer. Possible consequences of the catalytic methane hydrate formation on hydrate plug formation in gas pipelines, on large scale energy-efficient gas hydrate formation, and in planetary science are discussed. Peer reviewed: Yes NRC publication: Yes
format Article in Journal/Newspaper
author McLaurin, Graham
Shin, Kyuchul
Alavi, Saman
Ripmeester, John A.
author_facet McLaurin, Graham
Shin, Kyuchul
Alavi, Saman
Ripmeester, John A.
author_sort McLaurin, Graham
title Antifreezes act as catalysts for methane hydrate formation from ice
title_short Antifreezes act as catalysts for methane hydrate formation from ice
title_full Antifreezes act as catalysts for methane hydrate formation from ice
title_fullStr Antifreezes act as catalysts for methane hydrate formation from ice
title_full_unstemmed Antifreezes act as catalysts for methane hydrate formation from ice
title_sort antifreezes act as catalysts for methane hydrate formation from ice
publisher Wiley
publishDate 2014
url https://doi.org/10.1002/anie.201403638
https://nrc-publications.canada.ca/eng/view/object/?id=946fcd26-4c59-4998-b55d-0413c180e5d5
https://nrc-publications.canada.ca/fra/voir/objet/?id=946fcd26-4c59-4998-b55d-0413c180e5d5
genre Methane hydrate
genre_facet Methane hydrate
op_relation issn:1433-7851
Angewandte Chemie - International Edition, Volume: 53, Issue: 39, Publication date: 2014-09-24, Pages: 10429–10433
doi:10.1002/anie.201403638
op_doi https://doi.org/10.1002/anie.201403638
container_title Angewandte Chemie International Edition
container_volume 53
container_issue 39
container_start_page 10429
op_container_end_page 10433
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