Studying Methane Migration Mechanisms at Walker Ridge, Gulf of Mexico, Via 3D Methane Hydrate Reservoir Modeling


Book Description

We have developed a 3D methane hydrate reservoir simulator to model marine methane hydrate systems. Our simulator couples highly nonlinear heat and mass transport equations and includes heterogeneous sedimentation, in-situ microbial methanogenesis, the influence of pore size contrast on solubility gradients, and the impact of salt exclusion from the hydrate phase on dissolved methane equilibrium in pore water. Using environmental parameters from Walker Ridge in the Gulf of Mexico, we first simulate hydrate formation in and around a thin, dipping, planar sand stratum surrounded by clay lithology as it is buried to 295mbsf. We find that with sufficient methane being supplied by organic methanogenesis in the clays, a 200x pore size contrast between clays and sands allows for a strong enough concentration gradient to significantly drop the concentration of methane hydrate in clays immediately surrounding a thin sand layer, a phenomenon that is observed in well log data. Building upon previous work, our simulations account for the increase in sand-clay solubility contrast with depth from about 1.6% near the top of the sediment column to 8.6% at depth, which leads to a progressive strengthening of the diffusive flux of methane with time. By including an exponentially decaying organic methanogenesis input to the clay lithology with depth, we see a decrease in the aqueous methane supplied to the clays surrounding the sand layer with time, which works to further enhance the contrast in hydrate saturation between the sand and surrounding clays. Significant diffusive methane transport is observed in a clay interval of about 11m above the sand layer and about 4m below it, which matches well log observations. The clay-sand pore size contrast alone is not enough to completely eliminate hydrate (as observed in logs), because the diffusive flux of aqueous methane due to a contrast in pore size occurs slower than the rate at which methane is supplied via organic methanogenesis. Therefore, it is likely that additional mechanisms are at play, notably bound water activity reduction in clays. Three-dimensionality allows for inclusion of lithologic heterogeneities, which focus fluid flow and subsequently allow for heterogeneity in the methane migration mechanisms that dominate in marine sediments at a local scale. Incorporating recently acquired 3D seismic data from Walker Ridge to inform the lithologic structure of our modeled reservoir, we show that even with deep adjective sourcing of methane along highly permeable pathways, local hydrate accumulations can be sourced either by diffusive or advective methane flux; advectively-sourced hydrates accumulate evenly in highly permeable strata, while diffusively-sourced hydrates are characterized by thin strata-bound intervals with high clay-sand pore size contrasts.




Gas Hydrate Reservoirs and Associated Methane Migration Mechanisms on Continental Margins


Book Description

Natural gas hydrate has been studied for its natural gas storage capacity, its significant role in global carbon cycles and its possible link to continental margin submarine landslides. However, the role of gas hydrate systems in broad global processes is still not well understood due to the large uncertainties in the estimate of global distribution and concentration of gas hydrate. For a given marine geosystems, the location and volume of gas hydrate accumulations heavily rely on the methane migration mechanisms, which are important links between the gas source and gas hydrate reservoir in natural gas hydrate systems. Numerical models are a great tool to explore methane migration mechanisms for natural gas hydrate accumulations by providing a framework that combines the geophysical, geochemical, geobiological, and geological measurements. The goal of this dissertation is to apply methane transport-reaction models to better understand the mechanisms and key factors that control gas hydrate accumulations in different marine settings. In Chapter 2, I focus on gas hydrate formation in thin, isolated, coarse- grained layers and in surrounding fine-grained hydrate-free zones. I use the available geophysical logging data measured in Walker Ridge 313 (WR 313) Hole H and Hole G in the northern Gulf of Mexico, combined with advection- diffusion-reaction model to explore the hydrate formation mechanisms in the 3 m-thick Red Sand and the 4 m-thick Purple Sand. The advection-diffusion- reaction model involves aqueous methane diffusion, methane transport with water advection, and methane generation. I confirm that a short-range methane diffusion mechanism is able to explain the hydrate accumulations in thin layers and the hydrate-free zones in the surrounding muds. I show the key parameters that control the total amount of methane and hydrate formation within coarse- grained layers as well as the thickness of hydrate-free zones in the surrounding fine-grained muds. This work is published in Geochemistry, Geophysics, Geosystems, titled Factors Controlling Short-Range Methane Migration of Gas Hydrate Accumulations in Thin Coarse-Grained Layers. In Chapter 3, I describe in detail the time-dependent calculation of dissolved methane concentration and gas hydrate content in the advection- diffusion-reaction model. The partial differential equations for the mass balance of sedimentary organic carbon, methane, and hydrate are solved in terms of material derivatives. The material derivatives for each component are then solved applying a semi-Lagrangian finite difference method combined with a fractional step method, which is an effective mathematical method for solving advection problems. In addition, I show the key assumptions made in the development of the methane hydrate formation model in this work. In Chapter 4, I focus on high saturations (79-93% in pore volume) of hydrate formation in thick, coarse-grained sediments at Green Canyon 955 (GC 955) in the northern Gulf of Mexico. I use 1D and 2D numerical models and compare the predicted gas hydrate formation in coarse-grained layers with different mechanisms. I show that short-range methane diffusion and upward water advection are not enough to form high saturations of hydrate in the GC 955 reservoir, but the free gas flow is required to form high saturations of hydrate at GC 955. This work has been accepted to the special volume of American Association of Petroleum Geologists (AAPG) Bulletin, titled Methane Migration Mechanisms for The GC 955 Gas Hydrate Reservoir, Northern Gulf of Mexico. In Chapter 5, I focus on the gas hydrate system on the Hikurangi Margin, offshore New Zealand, where the reservoir is cm-thick, coarse-grained silts bounded with fine-grained muds that contain no hydrate. I show the estimation of the base of gas hydrate stability zone (GHSZ) applying temperature measurements from coring and logging and the hydrate phase boundaries calculated from Sloan and Koh (2008) and Tishchenko et al., 2005. The estimated depth to the base of GHSZ are compared to that applied in Pecher et al. (2018), Screaton et al. (2019), and Sultan (2019). In addition, I apply previously developed 1D microbial methanogenesis advection-diffusion- reaction model to test methane migration mechanisms to form hydrate reservoir at Hikurangi Margin. In Chapter 6, I summarize the effects of different methane transport mechanisms that are short-range diffusion, upward water advection, and free gas flow on gas hydrate accumulations in heterogeneous marine sediments. I conclude that hydrate distribution and volume in marine settings depends heavily on the methane migration mechanisms, but it is also controlled by the amount of methane supply and sediment heterogeneity.




Realizing the Energy Potential of Methane Hydrate for the United States


Book Description

Natural gas, composed mostly of methane, is the cleanest of all the fossil fuels, emitting 25-50% less carbon dioxide than either oil or coal for each unit of energy produced. In recent years, natural gas supplied approximately 20-25% of all energy consumed in the United States. Methane hydrate is a potentially enormous and as yet untapped source of methane. The Department of Energy's Methane Hydrate Research and Development Program has been tasked since 2000 to implement and coordinate a national methane hydrate research effort to stimulate the development of knowledge and technology necessary for commercial production of methane from methane hydrate in a safe and environmentally responsible way. Realizing the Energy Potential of Methane Hydrate for the United States evaluates the program's research projects and management processes since its congressional re-authorization in 2005, and presents recommendations for its future research and development initiatives.




Oceanic Methane Hydrates


Book Description

Methane hydrates are still a complicated target for today’s oil and gas offshore engineers, particularly the lack of reliable real field test data or obtaining the most recent technology available on the feasibility and challenges surrounding the extraction of methane hydrates. Oceanic Methane Hydrates delivers the solid foundation as well as today’s advances and challenges that remain. Starting with the fundamental knowledge on gas hydrates, the authors define the origin, estimations, and known exploration and production methods. Historical and current oil and gas fields and roadmaps containing methane hydrates around the world are also covered to help lay the foundation for the early career engineer. Lab experiments and advancements in numerical reservoir simulations transition the engineer from research to practice with real field-core sampling techniques covered, points on how to choose producible methane hydrate reservoirs, and the importance of emerging technologies. Actual comparable onshore tests from around the world are included to help the engineer gain clarity on field expectations.Rounding out the reference are emerging technologies in all facets of the business including well completion and monitoring, economics aspects to consider, and environmental challenges, particularly methods to reduce the costs of methane hydrate exploration and production techniques. Rounding out a look at future trends, Oceanic Methane Hydrates covers both the basics and advances needed for today’s engineers to gain the required knowledge needed to tackle this challenging and exciting future energy source. Understand real data and practice examples covering the newest developments of methane hydrate, from chemical, reservoir modelling and production testing Gain worldwide coverage and analysis of the most recent extraction production tests Cover the full range of emerging technologies and environmental sustainability including current regulations and policy outlook




Charting the Future of Methane Hydrate Research in the United States


Book Description

Methane hydrate is a natural form of clathrate - a chemical substance in which one molecule forms a lattice around a "guest" molecule with chemical bonding. In this clathrate, the guest molecule is methane and the lattice is formed by water to form an ice-like solid. Methane hydrate has become the focus of international attention because of the vast potential for human use worldwide. If methane can be produced from hydrate, a reasonable assumption given that there are no obvious technical or engineering roadblocks to commercial production, the nation's natural gas energy supply could be extended for many years to come. This report reviews the Department of Energy's (DOE) Methane Hydrate Research and Development Program, the project selection process, and projects funded to date. It makes recommendations on how the DOE program could be improved. Key recommendations include focusing DOE program emphasis and research in 7 priority areas; incorporating greater scientific oversight in the selection, initiation, monitoring, and assessment of major projects funded by the DOE; strengthening DOE's contribution to education and training through funding of fellowships, and providing project applicants with a set of instructions and guidelines outlining requirements for timely and full disclosure of project results and consequences of noncompliance.




The Interdependence of Lithologic Heterogeneity and Methane Migration on Gas Hydrate Formation in Marine Sediments


Book Description

Despite the ubiquity of methane hydrate in the pore space of shallow marine sediments worldwide, the processes governing the transport of methane from source to reservoir are still poorly understood. Methane migration mechanisms constitute important links in the evolution of a natural gas hydrate system because they control how gas hydrate distributes in sediment pore space as well as the quantities in which gas hydrate forms. Without a thorough understanding of methane migration, it is impossible to accurately predict how a methane source interacts with a reservoir, which makes it very difficult to reliably predict where hydrate will form in a given environment. When trying to understand a gas hydrate system as a potential natural gas prospect, as a geohazard, or as an agent of global climate change, it is essential to accurately characterize the distribution and volume of hydrate present. Thus, methane migration mechanisms must be properly understood if a hydrate system is to be evaluated for any of these purposes. The work presented here develops 3D, multiphase, multicomponent fluid transport simulation software to investigate the impact of three different methane migration mechanisms on the transport dynamics and distribution of gas hydrate in marine geosystems: diffusion, short-range advection, and methane recycling. I find that the expressions of gas hydrate systems in nature are sensitive to small-scale heterogeneities in sediment lithology and capillary effects. Properties of a hydrate-bearing unit including pore size distribution, unit thickness, dip, and proximity to other layers in multilayered systems all contribute to preferential flux of methane toward and within certain hydrate-bearing sediment strata, which impact the distribution of hydrate throughout these units. When sediments are overpressured, permeability contrasts can focus methane-charged fluids along high permeability pathways and precipitate hydrate through short-range advection. Capillary phenomena can produce a region near the base of the hydrate stability zone where hydrate, water, and free gas coexist over a range of pressures and temperatures, which can drive recycling of free gas derived from dissociated hydrate back into the hydrate stability zone




An Engineering Study to Investigate the Methane Hydrate Resource Potential Associated with the Barrow Gas Fields in Alaska


Book Description

"Previous studies on the Barrow Gas Fields (BGF) in Alaska have suggested that accumulations of natural gas hydrates could exist within these reservoirs. In consideration of future energy challenges, and the potential of gas hydrates in meeting them, a comprehensive engineering study was undertaken to investigate the BGF for hydrates, and to recommend an optimal plan for future field development. The methane hydrate resource potential of the BGF, viz. the East Barrow (EB), South Barrow (SB), and Walakpa (WAL) gas pools, was analyzed by developing gas hydrate stability models. Material balance studies were performed on the EB gas field to understand the reservoir drive mechanisms. Gas-water relative permeability experiments were conducted on a hydrate-saturated consolidated core sample, by maintaining the EB reservoir conditions, to model two-phase fluid flow behavior. Finally, field-scale dynamic reservoir simulation models were developed for the EB and WAL gas fields. Production history data were matched, reservoir drive mechanisms were confirmed, free gas and hydrate resources were quantified, hydrate dissociation patterns were examined, optimum locations for drilling infill wells were identified, and future production scenarios were simulated. Findings from this work indicate that BGF are associated with hydrates that are constantly recharging the gas reservoir by dissociation"--Leaf iii.




Numerical Investigations of the Fluid Flows at Deep Oceanic and Arctic Permafrost-Associated Gas Hydrate Deposits


Book Description

Methane hydrate is an ice-like solid which sequesters large quantities of methane gas within its crystal structure. The source of methane is typically derived from organic matter broken down by thermogenic or biogenic activity. Methane hydrate (or more simply, hydrate) is found around the globe within marine sediments along most continental margins where thermodynamic conditions and methane gas (in excess of local solubility) permit its formation. Hydrate deposits are quite possibly the largest reservoir of fossil fuel on Earth, however, their formation and evolution in response to changing thermodynamic conditions, such as global warming, are poorly understood. Upward fluid flow (relative to the seafloor) is thought to be important for the formation of methane hydrate deposits, which are typically found beneath topographic features on the seafloor. However, one-dimensional models predict downward flow relative to the seafloor in compacting marine sediments. The presence of upward flow in a passive margin setting can be explained by fluid focusing beneath topography when sediments have anisotropic permeability due to sediment bedding layers. Even small slopes (10 degrees) in bedding planes produce upward fluid velocity, with focusing becoming more effective as slopes increase. Additionally, focusing causes high excess pore pressure to develop below topographic highs, promoting high-angle fracturing at the ridge axis. Magnitudes of upward pore fluid velocity are much larger in fractured zones, particularly when the surrounding sediment matrix is anisotropic in permeability. Enhanced flow of methane-bearing fluids from depth provides a simple explanation for preferential accumulation of hydrate under topographic highs. Models of fluid flow at large hydrate provinces can be constrained by measurements of naturally-occurring radioactive tracers. Concentrations of cosmogenic iodine, 129-I, in the pore fluid of marine sediments often indicate that the pore fluid is much older than the host sediment. Old pore fluid age may reflect complex flow patterns, such a fluid focusing, which can cause significant lateral migration as well as regions where downward flow reverses direction and returns toward the seafloor. Longer pathlines can produce pore fluid ages much older than that expected with a one-dimensional compaction model. For steady-state models with geometry representative of Blake Ridge (USA), a well-studied hydrate province, pore fluid ages beneath regions of topography and within fractured zones can be up to 70 Ma old. Results suggest that the measurements of 129-I/127-I reflect a mixture of new and old pore fluid. However, old pore fluid need not originate at great depths. Methane within pore fluids can travel laterally several kilometers, implying an extensive source region around the deposit. Iodine age measurements support the existence of fluid focusing beneath regions of seafloor topography at Blake Ridge, and suggest that the methane source at Blake Ridge is likely shallow. The response of methane hydrate reservoirs to warming is poorly understood. The great depths may protect deep oceanic hydrates from climate change for the time being because transfer of heat by conduction is slow, but warming will eventually be felt albeit in the far future. On the other hand, unique permafrost-associated methane hydrate deposits exist at shallow depths within the sediments of the circum-Arctic continental shelves. Arctic hydrates are thought to be a relict of cold glacial periods, aggrading when sea levels are much lower and shelf sediments are exposed to freezing air temperatures. During interglacial periods, rising sea levels flood the shelf, bringing dramatic warming to the permafrost- and hydrate-bearing sediments. Permafrost-associated methane hydrate deposits have been responding to warming since the last glacial maximum ~18 kaBP as a consequence of these natural glacial cycles. This `experiment, ' set into motion by nature itself, allows us a unique opportunity to study the response of methane hydrate deposits to warming. Gas hydrate stability in the Arctic and the permeability of the shelf sediments to gas migration is thought to be closely linked with relict submarine permafrost. Submarine permafrost extent depends on several environmental factors, such as the shelf lithology, sea level variations, mean annual air temperature, ocean bottom water temperature, geothermal heat flux, groundwater hydrology, and the salinity of the pore water. Effects of submarine groundwater discharge, which introduces fresh terrestrial groundwater off-shore, can freshen deep marine sediments and is an important control on the freezing point depression of ice and methane hydrate. While several thermal modeling studies suggest the permafrost layer should still be largely intact near-shore, many recent field studies have reported elevated methane levels in Arctic coastal waters. The permafrost layer is thought to create an impermeable barrier to fluid and gas flow, however, talik formation (unfrozen regions within otherwise continuous permafrost) below paleo-river channels can create permeable pathways for gas migration from depth. This is the first study of its kind to make predictions of the methane gas flux to the water column from the Arctic shelf sediments using a 2D multi-phase fluid flow model. Model results show that the dissociation of methane hydrate deposits through taliks can supersaturate the overlying water column at present-day relative to equilibrium with the atmosphere when taliks are large (> 1 km width) or hydrate saturation is high within hydrate layers (> 50% pore volume). Supersaturated waters likely drive a net flux of methane into the atmosphere, a potent greenhouse gas. Effects of anthropogenic global warming will certainly increase gas venting rates if ocean bottom water temperatures increase, but likely won't have immediately observable impacts due to the long response times.




Complete Guide to Methane Hydrate Energy


Book Description

In March 2013, Japanese researchers announced a breakthrough in the extraction of natural gas from methane hydrates. This marked the latest important development in the quest for energy from methane hydrate, known as the ice that burns. This book presents a comprehensive collection of up-to-date publications about this vital new resource, covering all aspects of the field, including the possible effects of hydrate gas production on climate change. Contents include: Energy Resource Potential of Methane Hydrate; Methane Hydrate Program Report to Congress - October 2012; Interagency Coordination on Methane Hydrates R&D: Demonstrating the Power of Working Together; Report of the Methane Hydrate Advisory Committee on Methane Hydrate Issues and Opportunities including Assessment of Uncertainty of the Impact of Methane Hydrate on Global Climate Change; Report to Congress - An Assessment of the Methane Hydrate Research Program and An Assessment of the 5-Year Research Plan of the Department of Energy Prepared by the Federal Methane Hydrate Advisory Committee - June 2007; An Interagency Roadmap for Methane Hydrate Research and Development; Methane Hydrates R&D Program. Methane hydrate is a cage-like lattice of ice inside of which are trapped molecules of methane, the chief constituent of natural gas. If methane hydrate is either warmed or depressurized, it will revert back to water and natural gas. When brought to the earth's surface, one cubic meter of gas hydrate releases 164 cubic meters of natural gas. Hydrate deposits may be several hundred meters thick and generally occur in two types of settings: under Arctic permafrost, and beneath the ocean floor. Methane that forms hydrate can be both biogenic, created by biological activity in sediments, and thermogenic, created by geological processes deeper within the earth. While global estimates vary considerably, the energy content of methane occurring in hydrate form is immense, possibly exceeding the combined energy content of all other known fossil fuels. The U.S. Department of Energy methane hydrate program aims to develop the tools and technologies to allow environmentally safe methane production from arctic and domestic offshore hydrates. The program includes R&D in: Production Feasibility: Methane hydrates occur in large quantities beneath the permafrost and offshore, on and below the seafloor. DOE R&D is focused on determining the potential and environmental implications of production of natural gas from hydrates. Research and Modeling: DOE is studying innovative ways to predict the location and concentration of subsurface methane hydrate before drilling. DOE is also conducting studies to understand the physical properties of gas hydrate-bearing strata and to model this understanding at reservoir scale to predict future behavior and production. Climate Change: DOE is studying the role of methane hydrate formation and dissociation in the global carbon cycle. Another aspect of this research is incorporating GH science into climate models to understand the relationship between global warming and methane hydrates.




Modeling Investigation of Gas Hydrate Decomposition


Book Description

In the last few decades, there has been a great interest in the hydrate reservoirs for energy storage and source purposes. It has been proven that hydrates can contribute to ocean carbon cycling, global climate change, and coastal sediment stability. The permafrost and offshore environments contain enormous quantities of methane in the form of gas hydrates. In addition, the natural gas has been recently produced worldwide including in Alaska, Siberia, Japan, and North West Territories of Canada. However, the gas hydrates formation may lead to various forms of blockages in oil/gas production and transportation processes, resulting in high capital and operating costs. Detailed experimental and modeling investigations of hydrate formation and decomposition can assist to better understand the mechanisms involved in gas production from hydrates. Thus, it is important to determine the equilibrium hydrate-forming conditions so that a systematic parametric sensitivity analysis is conducted to identify the vital process and thermodynamic parameters affecting this occurrence. This project focuses on the hydrate formation/dissociation conditions where equations of state and molecular dynamic (MD) simulations are used. Giving further information, this study provides a reliable model to determine the gas hydrate formation and decomposition conditions of pure, binary, and ternary systems of hydrate gases where the van der Waals Platteuw model is utilized by combining with extended UNIQUAC model and PC-SAFT equation of state. In addition, MD simulations are conducted to investigate the microscopic mechanisms/phenomena and intermolecular forces involved in gas (pure and mixture) hydrate decomposition, where the molecular interactions, structures, and behaviours of hydrate systems need to be appropriately explored. Through a systematic design of simulation runs, the impacts of temperature, pressure, cage occupancy, and inhibitors on the hydrate dissociation are studied. Furthermore, the diffusion coefficient, density, and heat capacity of gas hydrates with different structures and compositions of methane, carbon dioxide, propane, and isobutane are determined through employing MD strategy. A very good agreement is noticed between the modeling results and the experimental data so that the value of AADT% for PC-SAFT equation of state is lower, compared to the previous EOS/thermodynamic models. The binary interaction parameters for different binary components are investigated by using experimental hydrate data, leading to better outcome compared with results obtained through fitting the VLE data. The trend of the heat capacity and density of methane hydrate obtained from the MD simulations shows a good match with the real data. The hydrate decomposition is not achieved at the equilibrium temperature at 100% cage occupancy; however, the decomposition of the methane hydrate lattice is observed when the cage occupancy reduces from 100% to 87.5% or 75% because of low stability and high diffusion coefficient of the methane molecules at low cage occupancies where the temperature and pressure are constant. The lattice parameter for the methane/water and methane/isobutane systems is calculated at a variety of pressures and temperatures. A good agreement between the experimental data and simulation results is noticed. The relative importance of inhibitors in terms of gas hydrate decomposition duration is assessed. Based on this criterion, the inhibitors are ordered as follows: methanol > ethanol >glycerol. The physical properties such as density and lattice parameter for different compositions of methane + carbon dioxide are obtained which are in agreement with those determined by experimental and theoretical techniques. According to the MD results, the structure with methane (25%) + carbon dioxide (75%) composition is almost stable under 300 K at 5 MPa; it means the best configuration to have a stable structure is when carbon dioxide and methane molecules are in large and small cavities, respectively. MD technique is used to investigate the bubble formation and evolution of carbon dioxide and methane after dissociation. Analysing the outcome of the present and previous works, the current study provides new reliable/useful information and data on the thermodynamic behaviours and molecular level of the hydrate dissociation process. It is expected that such a research investigation offers effective tips/guidelines to deal with hydrate formation and dissociation in terms of utilization, prevention, and processing.