氢相互作用在大体积流体地质储存中的应用

Sidi Mamoudou, Son Dang, Chandra Rai
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引用次数: 0

摘要

地质储氢是脱碳的关键组成部分,可以实现大规模的能源储存,并支持向低碳经济的过渡。通过在地下储层(如枯竭的油气储层)中长期储存氢气,地质储存提高了能源安全性,并稳定了能源供应。这项研究是研究饱和多孔岩石中氢相互作用的初步步骤,重点是利用核磁共振(NMR)研究储层流体中的氢行为。测试流体包括水、十二烷油(轻油)、死油和沸石蜡(重油),压力可达1800 psi。此外,由于氘化水和全氟HT-230的核磁共振信号可以忽略不计,因此用作控制流体。HT-230通常用作岩心桥塞测量中的围封流体,也为比较提供了基准。根据分子相互作用,T₂弛豫时间可以作为区分散装液体中游离氢和溶解氢的代理。由于它对流体中的氢质子很敏感,因此它被用来评估粘度和密度等体积特性的变化。结果表明,氢在与水相互作用时主要停留在自由相,这可以通过快速弛豫时间(1-20 ms)来证明,并且没有观察到T₂随压力的变化,证实了有限的溶解。同样,碳氢化合物——包括十二烷、死油和蜡——在核磁共振下没有显示氢溶解的证据,因为只检测到自由相氢信号(1-20 ms)。然而,对死油中气泡的视觉观察表明,物理上的氢捕获而不是真正的分子溶解,表明氢保留在分离的气相中,而没有完全融入液相。在全氟HT-230中,中间的T₂弛豫信号(100-300 ms)表明可能存在氢溶解,室温下估计体积为0.80-1.20 ± 0.02 cc。这一发现表明,虽然HT-230通常是惰性的,但可能会发生某种程度的氢相互作用。因此,在应力作用下的岩心塞测试中,使用HT-230作为围封流体时,建议谨慎使用,否则应将该信号排除在分析之外。虽然这项研究是在相对较低的温度和较短的实验时间内进行的,但在我们的测试条件下,氢可以物理地困在死油中。这些结果提供了对散装流体中H₂相互作用的基本理解,为未来在枯竭油气藏中测量芯塞的氢保留、扩散和流动性提供了依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hydrogen interaction in bulk fluids for geological storage application using NMR
Hydrogen geostorage is a crucial component of decarbonization, enabling large-scale energy storage and supporting the transition to a low-carbon economy. By allowing long-term hydrogen storage in subsurface formations such as depleted oil and gas reservoirs, geostorage enhances energy security and stabilizes energy supply. This study serves as a preliminary step before investigating H₂ interactions in saturated porous rocks, focusing on hydrogen behavior in reservoir fluids using nuclear magnetic resonance (NMR). The tested fluids include water, dodecane oil (light oil), dead oil, and ozokerite wax (heavy oil) under pressures up to 1800 psi. Additionally, deuterated water and perfluorinated HT-230 were used as control fluids due to their negligible NMR signals. HT-230, commonly used as a confining fluid in core plug measurements, also provides a baseline for comparison. T₂ relaxation times served as a proxy for distinguishing free hydrogen from dissolved hydrogen in bulk liquid based on molecular interactions. Since it is sensitive to hydrogen protons in fluids, it was used to assess changes in bulk properties such as viscosity and density. The results indicate that hydrogen predominantly remains in the free phase when interacting with water, as evidenced by fast relaxation times (1–20 ms) and no observed changes in T₂ with pressure, confirming limited dissolution. Similarly, hydrocarbons—including dodecane, dead oil, and wax—showed no evidence of hydrogen dissolution under NMR, as only free-phase hydrogen signals (1–20 ms) were detected. However, visual observations of gas bubbles in dead oil suggest physical hydrogen trapping rather than true molecular dissolution, indicating hydrogen retention in a discrete gas phase without full integration into the liquid phase. In perfluorinated HT-230, an intermediate T₂ relaxation signal (100–300 ms) suggests possible hydrogen dissolution, with an estimated volume of 0.80–1.20 ± 0.02 cc at room temperature. This finding indicates that while HT-230 is generally inert, some level of hydrogen interaction may occur. Therefore, caution is advised when using HT-230 as a confining fluid in core plug tests under stress, or this signal should be excluded from analysis. Although this study was conducted at relatively low temperatures and over short experimental durations, hydrogen can be physically trapped in dead oil within our test conditions. These results provide a baseline understanding of H₂ interactions in bulk fluids, informing future core plug measurements of hydrogen retention, diffusion, and mobility in depleted oil and gas reservoirs.
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