笼状水合物
盐(化学)
化学
二氧化碳
石英
甲烷
体积热力学
化学工程
矿物学
水合物
地质学
热力学
有机化学
物理
工程类
古生物学
作者
Rita Giovannetti,Alberto Maria Gambelli,Beatrice Castellani,Andrea Rossi,Marco Minicucci,Marco Zannotti,Yan Li,Federico Rossi
标识
DOI:10.1016/j.molliq.2022.119300
摘要
The equilibria of methane and carbon dioxide clathrate hydrates were measured in presence of a pure-quartz porous sand, with and without NaCl. Two different salt concentrations were tested: 0.030 and 0.037 wt%. Results were compared with phase equilibrium data already present in literature for these species. Despite salt, the porous medium was found to promote the process, mainly for the increased surface/volume ratio and for the improved heat transfer. In presence of salt, sand affected the process differently as a function of temperature: at values higher than 3 – 5 °C, it promoted the process, while for values lower than this range, but still greater than the ice-point, it acted as an inhibitor. However, these results can be considered true only for temperatures above the ice point. Due to similarity of ice water with clathrate hydrates, Raman microscale measurements were performed to gather information about the influence of sediments, salt, and temperature on OH-stretching vibrations of water. The obtained results allowed to clarify how the addition of NaCl, and or sediments to liquid water, under different temperature conditions (15 °C and −15 °C), influenced the water hydrogen bonds. Specifically, the changes of OH-stretching vibrations, when correlated with the NaCl concentrations, demonstrated that the presence of sediments partially inhibited the salt effects in the ice water probably due to hydrophilic interactions with the silanol groups of sediments. SEM measurements showed morphological information on sediments and on ice in different experimental conditions.
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