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Modeling Fluid Flow Effects on Shallow Pore Water Chemistry and Methane Hydrate Distribution in Heterogeneous Marine Sediment.

机译:模拟流体流动对非均质海洋沉积物中浅孔水化学和甲烷水合物分布的影响。

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摘要

The depth of the sulfate-methane transition (SMT) above gas hydrate systems is a direct proxy to interpret upward methane flux and hydrate saturation. However, two competing reaction pathways can potentially form the SMT. Moreover, the pore water profiles across the SMT in shallow sediment show broad variability leading to different interpretations for how carbon, including CH4, cycles within gas-charged sediment sequences over time. The amount and distribution of marine gas hydrate impacts the chemistry of several other dissolved pore water species such as the dissolved inorganic carbon (DIC). A one-dimensional (1-D) numerical model is developed to account for downhole changes in pore water constituents, and transient and steady-state profiles are generated for three distinct hydrate settings. The model explains how an upward flux of CH4 consumes most SO2-4 at a shallow SMT implying that anaerobic oxidation of methane (AOM) is the dominant SO2-4 reduction pathway, and how a large flux of 13C-enriched DIC enters the SMT from depth impacting chemical changes across the SMT. Crucially, neither the concentration nor the δ13C of DIC can be used to interpret the chemical reaction causing the SMT.;The overall thesis objective is to develop generalized models building on this 1-D framework to understand the primary controls on gas hydrate occurrence. Existing 1-D models can provide first-order insights on hydrate occurrence, but do not capture the complexity and heterogeneity observed in natural gas hydrate systems. In this study, a two-dimensional (2-D) model is developed to simulate multiphase flow through porous media to account for heterogeneous lithologic structures (e.g., fractures, sand layers) and to show how focused fluid flow within these structures governs local hydrate accumulation. These simulations emphasize the importance of local, vertical, fluid flux on local hydrate accumulation and distribution. Through analysis of the fluid fluxes in 2-D systems, it is shown that a local Peclet number characterizes the local hydrate and free gas saturations, just as the Peclet number characterizes hydrate saturations in 1-D, homogeneous systems. Effects of salinity on phase equilibrium and co-existence of hydrate and gas phases can also be investigated using these models.;Finally, infinite slope stability analysis assesses the model to identify for potential subsea slope failure and associated risks due to hydrate formation and free gas accumulation. These generalized models can be adapted to specific field examples to evaluate the amount and distribution of hydrate and free gas and to identify conditions favorable for economic gas production.
机译:天然气水合物系统上方的硫酸盐-甲烷过渡(SMT)深度是解释甲烷向上通量和水合物饱和度的直接代理。但是,两个相互竞争的反应路径可能会形成SMT。此外,浅层沉积物中整个SMT的孔隙水剖面显示出广泛的变化性,导致对含CH4的碳如何在含气沉积物序列内随时间循环的解释不同。海水水合物的数量和分布会影响其他几种溶解的孔隙水物种的化学,例如溶解的无机碳(DIC)。建立一维(1-D)数值模型来考虑孔隙水成分的井下变化,并针对三种不同的水合物设置生成瞬态和稳态剖面。该模型解释了在浅层SMT中CH4的向上通量是如何消耗大部分SO2-4的,这意味着甲烷的厌氧氧化(AOM)是主要的SO2-4还原途径,以及大量的13C富集DIC是如何从中进入SMT的。深度影响整个SMT的化学变化。至关重要的是,DIC的浓度和δ13C都不能用来解释引起SMT的化学反应。总体目标是在此1-D框架上建立通用模型,以了解天然气水合物发生的主要控制因素。现有的一维模型可以提供有关水合物发生的一阶见解,但不能捕获天然气水合物系统中观察到的复杂性和非均质性。在这项研究中,建立了二维(2-D)模型以模拟通过多孔介质的多相流,以解释非均质岩性结构(例如,裂缝,砂层),并显示这些结构中的集中流体流如何控制局部水合物。积累。这些模拟强调了局部,垂直,流体通量对局部水合物积累和分布的重要性。通过分析二维系统中的流体通量,可以看出,局部派克雷特数表征了局部水合物和自由气体的饱和度,正如派克雷特数表征了一维,均质系统中的水合物饱和度一样。也可以使用这些模型研究盐度对相平衡以及水合物和气相共存的影响。最后,无限边坡稳定性分析评估该模型,以识别潜在的海底边坡破坏以及由水合物形成和游离气引起的相关风险。积累。这些通用模型可以适应特定领域的示例,以评估水合物和游离气体的数量和分布,并确定有利于经济天然气生产的条件。

著录项

  • 作者

    Chatterjee, Sayantan.;

  • 作者单位

    Rice University.;

  • 授予单位 Rice University.;
  • 学科 Geology.;Geochemistry.;Engineering Chemical.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 284 p.
  • 总页数 284
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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