海水
甲烷
水合物
吸附
笼状水合物
超纯水
成核
纳米孔
人工海水
化学工程
化学
化学计量学
活性炭
无机化学
地质学
有机化学
海洋学
工程类
作者
Carlos Cuadrado‐Collados,François Fauth,I. Such-Basáñez,Manuel Martínez Escandell,Joaquín Silvestre-Alberó
标识
DOI:10.1016/j.micromeso.2017.07.047
摘要
Methane hydrate formation studies in saline environment show that activated carbons are excellent host structures able to promote the water-to-hydrate conversion. Under confinement conditions, methane hydrate formation takes place at mild temperatures (−10 °C), low pressures (<6 MPa), with extremely fast kinetics (within minutes) and with a large adsorption capacity (up to 66 wt% CH4 for seawater, i.e. a 128% improvement compared to the dry carbon). Similar studies using ultrapure water give rise to a total methane adsorption capacity of 93 wt%, i.e. entropic effects exerted by salt play a crucial role in the methane hydrate nucleation and growth. Synthesized methane hydrates exhibit a sI crystal structure and a stoichiometry that mimics natural hydrates. These findings open the gate towards the application of activated carbons with a highly developed nanoporous network as host structure for offshore methane storage in marine reservoirs.
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