非常规储层中的甲烷吸附问题—吸附量定义及各相态随压力变化

Revisit of methane adsorption in unconventional reservoirs: definitions and variation of phases with pressure

  • 摘要: 甲烷的吸附是非常规气藏的成藏及开发过程中的关键议题之一,而吸附相关理论涉及多学科交叉,进一步加深对其的理解有助于试验数据的合理解释及与吸附相关地质过程的分析。通过一个简易的吸附模型演示甲烷在储层条件下在石墨表面的吸附过程,非常规天然气储层中甲烷吸附过程中各相态的体积、密度及不同定义的吸附量变化过程得以精细展示。吸附相指吸附上下界内的相态,对应的量为绝对吸附量;过剩吸附量是指表面吸附对自由相的过剩,仅为一个数值而非相态,不影响自由相的分布及密度。储层条件下甲烷为超临界状态,过剩吸附主要由最靠近表面的一层流体贡献,低压阶段吸附相范围、密度与自由相均随压力的升高而线性增加,但在4~5 MPa后吸附相密度增速开始降低,至自由相与吸附相密度增速相当时,过剩吸附量、吸附相体积达到最大值,吸附层厚度最大时略大于一个甲烷分子直径,而后过剩吸附量、吸附相体积进入下降阶段,绝对吸附量则继续上升。在30~100 MPa,绝对吸附量大体恒定,而此时吸附相边界持续降低,即吸附相体积随压力的增加而降低,从而吸附相密度持续升高。若压力继续增加,吸附相可进一步致密化,从而导致过剩吸附量在降低到最小值后再次上升。在应用上,正确理解吸附相范围对绝对吸附量、吸附相密度等关键参数的求取影响,以更精确地评估含气量、计算产能。

     

    Abstract: The methane physisorption is one of the key issues discussed for the accumulation and exploration of unconventional reservoirs. Due to its multidisciplinary nature, a deeper understanding of the detailed adsorption mechanism is crucial for geological applications. By constructing a representative methane − graphite adsorption system, the detailed variation of key parameters during adsorption process with the increase of pressure is further discussed, including excess and absolute adsorption amount, adsorption phase volume, and density. Adsorption phase is confined between lower and upper phase boundaries, within which is the absolute amount absorbed. Surface excess represents the amount of adsorption phase exceeding the bulk phase at the same density, rather than a phase that exists, and the surface excess do not disturb the distribution of bulk phase. In reservoirs, methane is supercritical, the adjacent layer of the surface mainly contributes the excess adsorption. The amount of absolute adsorption, the volume of adsorption phase, as well as the bulk phase rise with the increase of pressure linearly for low pressures, but the increase rate of adsorption phase density begins to decelerate at 4−5 MPa while the bulk density keeps building up. When the increasing rate of bulk density catches up with that of adsorption phase, the surface excess and the volume of adsorption phase reaches their maximum and subsequently decline, the maximum thickness of adsorption phase is slightly bigger than the diameter of methane molecule. However, the absolute amount absorbed keeps rising until it plateaus between 30−100 MPa, during which pressure range the surface excess, upper absorption phase boundary, along with the absorption phase volume decrease with the rising pressure. For pressure higher than 100 MPa, the surface excess would drop to minimum and then increase again because of the continuous densification of the adsorption and bulk phases. For engineering application, a deeper understanding of the intricate characteristics of the adsorption phase would have a significant impact on the calculation of absolute adsorption amount and corresponding phase density, thus enabling a more accurate assessments of the gas in place and productivity.

     

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