4.6 Article

Experimental Investigation To Elucidate Why Tetrahydrofuran Rapidly Promotes Methane Hydrate Formation Kinetics: Applicable to Energy Storage

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 120, Issue 51, Pages 29062-29068

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.6b11995

Keywords

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Funding

  1. Energy Innovation Research Programme (EIRP) [NRF2015EWTEIRP002-002]
  2. National Research Foundation (NRF), Singapore

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Methane storage as SNG (solidified natural gas) in the form of clathrate hydrates is an emerging, economically feasible and environmentally benign technology for large scale storage. Mixed tetrahydrofuran (THF)-methane (CH4) hydrates offer a paradigm shift to milder storage conditions and faster hydrate formation kinetics, providing a promising scenario to scale up the SNG technology. In this work, we synthesize mixed THF-CH4 hydrates in a high pressure microdifferential scanning calorimeter (HP mu-DSC) to elucidate the two-step hydrate formation mechanism of mixed THF-CH4 hydrate identifying the synergism between THF and CH4. Heat flow change during hydrate formation and dissociation of mixed THF-CH4 hydrates formed in the presence of 5.56 mol % THF (stoichiometric composition) were monitored. The two step-mechanism of mixed THF-CH4 hydrate formation was further confirmed by the pressure-temperature profile and visual observations with a sample volume scale -up of about 350 times that of mu-DSC experiments.

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