水合物
笼状水合物
拉曼光谱
化学
海水
二氧化碳
甲烷
超纯水
天然气
晶格常数
晶体结构
化学工程
矿物学
材料科学
结晶学
纳米技术
衍射
地质学
有机化学
工程类
物理
光学
海洋学
作者
Andrea Rossi,Michele Ciulla,Valentino Canale,Marco Zannotti,Marco Minicucci,Pietro Di Profio,Rita Giovannetti
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2023-11-15
卷期号:37 (23): 18968-18976
被引量:8
标识
DOI:10.1021/acs.energyfuels.3c02991
摘要
Gas hydrates (GHs) are solid, ice-like compounds composed of water molecules forming a lattice structure that hosts gas molecules, produced under high pressure and low temperature. The structure of the hydrate structure is affected by the surrounding environment, and in this context, a structural characterization of GHs prepared in different environments, ultrapure (UP) water, seawater, synthetic sand, natural sand, and sodium dodecyl sulfate, has been proposed. In particular, the Raman spectroscopy has been used to investigate the structural changes in the water cages, the gas uptake in the hydrate structure, the CH4 cage occupancies, the hydration number, and the yield of carbon dioxide replacement at constant pressure. For this comparison, CH4-hydrates, CO2-hydrates, and CH4/CO2-hydrates (obtained from an implemented replacement process) were prepared in five different experimental conditions mentioned above and structurally characterized. From Raman investigation, pure CH4-hydrates displayed almost full (>95%) occupation in the large cage and a significant change in the small cage occupation related to the different tested media. The cage occupancy calculation of CO2/CH4-hydrates showed that a higher yield of replacement can be obtained in UP water and that CH4-hydrates in natural sand and in seawater, which are the most representing of natural environments, displayed a good replacement of CH4 with CO2. Additionally, the ex situ morphological characterization of the GHs by scanning electron microscopy (SEM) allowed the highlighting of morphological differences among the investigated samples.
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