FEATURES OF DECOMPOSITION OF GAS HYDRATE IN NONEQUILIBRIUM MODE IN A POROUS MEDIUM

M. Khasanov, S. R. Kildibaeva, M. Stolpovsky
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Abstract

The paper presents a mathematical model of the nonequilibrium decomposition of a gas hydrate contained in a porous reservoir of finite extent. The system of basic equations, which includes the law of conservation of mass, the heat inflow equation and Darcy’s law, also contains an equation describing the kinetics of nonequilibrium hydrate decomposition, which is determined by pressure, temperature and surface area of particles. On the basis of the numerical solution of the problem, dependences are obtained that allow us to identify the regularities of the process of nonequilibrium decomposition of gas hydrate in a natural reservoir when warm gas is injected into a porous reservoir. It is shown that at the initial moments of time after the start of injection, the extent of the region saturated with gas, hydrate and water is very small compared to the extent of the formation, which corresponds to the mode of hydrate decomposition on the frontal surface. At long injection times, the nonequilibrium hydrate decomposition process is characterized by the formation of three characteristic zones: the near one, where the pores are saturated with gas and water, the far one, saturated with methane and its gas hydrate, and the intermediate one, where gas, hydrate and water are located. It is established that the pressure and temperature in the extended region are connected by the condition of phase equilibrium. The influence of the main parameters of the system on the distributions of pressure, temperature, water saturation and hydrate saturation, as well as on the dynamics of their changes over time, is analyzed. It is shown that injection pressure, as well as reservoir permeability and porosity have a significant effect on the decomposition rate of gas hydrate. An increase in the values of these parameters contributes to an increase in the rate of nonequilibrium hydrate decomposition. An increase in the injection temperature leads only to an increase in the extent of the area containing methane and water.
气体水合物在多孔介质中的非平衡分解特征
本文介绍了有限范围多孔储层中气体水合物非平衡分解的数学模型。基本方程系统包括质量守恒定律、热量流入方程和达西定律,还包括一个描述非平衡水合物分解动力学的方程,该动力学由压力、温度和颗粒表面积决定。在对问题进行数值求解的基础上,我们获得了一些相关因素,从而可以确定在向多孔储层注入暖气时,天然储层中天然气水合物非平衡分解过程的规律性。结果表明,在注入开始后的初始时刻,气体、水合物和水的饱和区域范围与地层范围相比非常小,这与正面的水合物分解模式相对应。在较长的注入时间内,非平衡水合物分解过程的特点是形成三个特征区:近区,孔隙中气体和水饱和;远区,甲烷及其气体水合物饱和;中间区,气体、水合物和水位于其中。研究表明,扩展区域的压力和温度与相平衡条件有关。分析了系统主要参数对压力、温度、水饱和度和水合物饱和度分布的影响,以及它们随时间的动态变化。结果表明,注入压力以及储层渗透率和孔隙度对天然气水合物的分解率有显著影响。这些参数值的增加会导致非平衡水合物分解率的增加。注入温度的提高只会导致含甲烷和水的区域范围扩大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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