Natural gas storage in hydrates in the presence of thermodynamic hydrate promoters: Review and experimental investigation

IF 2.7 3区 工程技术 Q3 CHEMISTRY, PHYSICAL Fluid Phase Equilibria Pub Date : 2025-04-01 Epub Date: 2024-11-17 DOI:10.1016/j.fluid.2024.114286
Yu Wei , Joshua Worley , Luis E. Zerpa , Yu-Chien (Alice) Chien , Derek Dunn-Rankin , Michael T. Kezirian , Carolyn A. Koh
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Abstract

Natural gas (NG), the cleanest fossil fuel, is playing an increasingly important role in the current energy supply. However, the safe storage and transportation of flammable NG is a long-standing challenge. Furthermore, NG emission has a stronger per molecule greenhouse effect on the environment than CO2. Therefore, efficient and effective methods of NG storage and transportation are needed. Storing NG in the form of gas hydrate offers advantages over common compression or liquefaction methods, but the thermodynamic conditions required for gas hydrate formation hinder the large-scale application of solidified natural gas (SNG) technology. This work presents a review of phase equilibrium conditions of gas hydrates formed by greenhouse gases including CH4, CO2 and NG in the presence of thermodynamic hydrate promoters. This study uses available thermodynamic software to calculate gas hydrate phase equilibrium using different Equations of State (EoS). We include an experimental investigation using a 2 L autoclave reactor to evaluate the effect of mass transfer, the presence of cyclopentane as a thermodynamic promoter, and the level of subcooling on the NG hydrate formation kinetics. The results show that: 1) Tetrahydrofuran and cyclopentane generally have the strongest thermodynamic-promoting effect; 2) Thermodynamic promotion of cyclopentane on NG hydrate is validated experimentally; 3) NG hydrate formation kinetics is greatly influenced by mechanical stirring (mass transfer), cyclopentane as a co-former and its concentration and subcooling; 4) At high subcooling, cyclopentane-promoted systems show a significantly improved gas storage capacity than the baseline sample; and 5) NG hydrate particles have a size distribution of hundreds of microns under current experimental conditions. This study offers new insight into NG hydrate formation thermodynamics and kinetics that has application to SNG technology.

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存在热力学水合物促进剂的水合物中的天然气储存:综述和实验研究
天然气(NG)是最清洁的化石燃料,在当前的能源供应中发挥着越来越重要的作用。然而,易燃天然气的安全储存和运输是一个长期存在的挑战。此外,NG排放对环境的每分子温室效应强于CO2。因此,需要高效、有效的天然气储运方法。以天然气水合物的形式储存天然气比常见的压缩或液化方法具有优势,但天然气水合物形成所需的热力学条件阻碍了固化天然气(SNG)技术的大规模应用。本文综述了甲烷、二氧化碳和天然气等温室气体在热力学水合物促进剂作用下形成天然气水合物的相平衡条件。本研究利用现有的热力学软件,利用不同的状态方程(EoS)计算天然气水合物的相平衡。我们使用2l高压釜反应器进行了实验研究,以评估传质、环戊烷作为热力学促进剂的存在以及过冷水平对NG水合物形成动力学的影响。结果表明:1)四氢呋喃和环戊烷的热力学促进作用普遍最强;2)实验验证了环戊烷对天然气水合物的热力学促进作用;3)机械搅拌(传质)、环戊烷共成体及其浓度和过冷对天然气水合物形成动力学影响较大;4)在高过冷状态下,环戊烷促进体系的储气能力比基线样品显著提高;5)在目前的实验条件下,NG水合物颗粒的尺寸分布为数百微米。该研究为天然气水合物形成热力学和动力学提供了新的见解,可应用于天然气制气技术。
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来源期刊
Fluid Phase Equilibria
Fluid Phase Equilibria 工程技术-工程:化工
CiteScore
5.30
自引率
15.40%
发文量
223
审稿时长
53 days
期刊介绍: Fluid Phase Equilibria publishes high-quality papers dealing with experimental, theoretical, and applied research related to equilibrium and transport properties of fluids, solids, and interfaces. Subjects of interest include physical/phase and chemical equilibria; equilibrium and nonequilibrium thermophysical properties; fundamental thermodynamic relations; and stability. The systems central to the journal include pure substances and mixtures of organic and inorganic materials, including polymers, biochemicals, and surfactants with sufficient characterization of composition and purity for the results to be reproduced. Alloys are of interest only when thermodynamic studies are included, purely material studies will not be considered. In all cases, authors are expected to provide physical or chemical interpretations of the results. Experimental research can include measurements under all conditions of temperature, pressure, and composition, including critical and supercritical. Measurements are to be associated with systems and conditions of fundamental or applied interest, and may not be only a collection of routine data, such as physical property or solubility measurements at limited pressures and temperatures close to ambient, or surfactant studies focussed strictly on micellisation or micelle structure. Papers reporting common data must be accompanied by new physical insights and/or contemporary or new theory or techniques.
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