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

被引:61
|
作者
Kumar, Asheesh [1 ]
Daraboina, Nagu [2 ]
Kumar, Rajnish [3 ]
Linga, Praveen [1 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 117585, Singapore
[2] Univ Tulsa, McDougall Sch Petr Engn, Tulsa, OK 74104 USA
[3] CSIR, Natl Chem Lab, Chem Engn & Proc Dev Div, Pune, Maharashtra, India
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2016年 / 120卷 / 51期
基金
新加坡国家研究基金会;
关键词
DIFFERENTIAL SCANNING CALORIMETRY; GAS HYDRATE; MOLECULAR-DYNAMICS; PRESSURE; DECOMPOSITION; WATER; DSC; VERIFICATION; NUCLEATION; MIXTURE;
D O I
10.1021/acs.jpcc.6b11995
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:29062 / 29068
页数:7
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