期刊
ENERGY & FUELS
卷 33, 期 2, 页码 1422-1432出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.energyfuels.8b03108
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资金
- National Key Research and Development Plan of China [2017YFC0307306]
- National Natural Science Foundation of China [51376182, 41473063]
- CAS Program [KGZD-EW-301]
- Open Fund of State Key Laboratory of Oil and Gas Reservoir Geology and Exploitation (Chengdu University of Technology) [PLC20190605]
The kinetic effects of several kinds of ionic liquids (ILs) on the formation of methane hydrate were experimentally investigated on both the macroscale and microscale levels. These ILs were 1-ethyl-3-methylimidazolium tetrafluoroborate ([EMIm]-BF4), 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIm]-BF4), 1-butyl-3-methylimidazolium iodide ([BMIm]-I), and N-butyl-N-methylpyrrolidinium tetrafluoroborate ([Py14]-BF4). Formation temperature, max subcooling, induction time, and growth rate of methane gas hydrates were used to evaluate the kinetic effects of ionic liquids in a high-pressure cell and flow loop. As evaluated from the indicator of the formation temperature in the high-pressure cell, the sequence of inhibition performance of ILs was as follows: pure water < 1 wt % [EMIm]-BF4 < 1 wt % PVP < 1 wt % [BMIm]-I < 1 wt % [BMIm]-BF4 < 1 wt % [Py14]-BF4. ILs could not slow the growth rates of methane hydrate effectively and even promote the gas consumption rates irrespective of in a high-pressure cell or flow loop. RXRD spectra showed that ILs could not change the structure of methane hydrate. Cryo-scanning electron microscopy images showed that there was a porous texture of methane hydrate containing ILs. Raman spectra showed that ILs interact with the cages of methane hydrate.
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