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Methane hydrate formation in the confined nanospace of activated carbons in seawater environment

机译:海水环境中激活碳的狭窄纳米环甲烷水合物形成

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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 degrees 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 sl 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. (C) 2017 Elsevier Inc. All rights reserved.
机译:盐水环境中的甲烷水合物形成研究表明,活性碳是优异的宿主结构,能够促进水 - 水合物转化。在限制条件下,甲烷水合物形成在温和的温度(-10℃),低压力(<6MPa)下进行,具有极快的动力学(分钟内)和吸附能力大(海水最高66wt%CH 4) ,即与干碳相比的128%改善)。使用超纯水的类似研究导致总甲烷吸附能力为93wt%,即盐施加的熵效应在甲烷水合物成核和生长中发挥至关重要的作用。合成的甲烷水合物表现出SL晶体结构和模拟天然水合物的化学计量。这些发现在高度发达的纳米多孔网络中打开了浇口,作为海洋水库海上甲烷储存的宿主结构。 (c)2017年Elsevier Inc.保留所有权利。

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