Self-Organized Colloids Thermodynamically Weaken the Effect of Salt on Methane Hydrate Formation

Natural gas hydrate deposits are typically rich in organic matter; they together with the host sediments play a crucial role in the nucleation and accumulation of gas hydrates, yet their potential thermodynamic effect on hydrate formation is rarely studied. In the present work, it was found that the...

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Bibliographic Details
Main Authors: Yanzhen Liu (3210600), Yu Feng (445691), Yang Zhao (39052), Lei Yang (102719), Hongsheng Dong (6507788), Lunxiang Zhang (6507791), Jiafei Zhao (3757111)
Format: Other Non-Article Part of Journal/Newspaper
Language:unknown
Published: 2021
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Online Access:https://doi.org/10.1021/acssuschemeng.1c02179.s001
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Summary:Natural gas hydrate deposits are typically rich in organic matter; they together with the host sediments play a crucial role in the nucleation and accumulation of gas hydrates, yet their potential thermodynamic effect on hydrate formation is rarely studied. In the present work, it was found that the deprotonated organic compounds could self-organize with the cations in the solution, forming organic colloids via coordination bonds. Elemental mapping showed that these organic colloids were filled with Ca 2+ and Na + ions as well as more concentrated organic matter surrounded by thin rings of Mg 2+ and Cl – ions. This was found to result in a concentration decrease of Ca 2+ and Na + ions in the solution with the presence of the colloids; the resulting decreased electrostatic effect of salt ions on water molecules would subsequently relieve the energy barrier of hydrate formation, showing a shift of the phase equilibrium conditions to a milder situation. This finding would be more nontrivial in low-permeability hydrate layers where mass exchange with the abundant ions in the seawater could be rather sluggish. The results could be of help in determining the local thickness and location of the gas hydrate stability zone and thereby the estimated reserves.