As the foundation of energy industry moves towards gas, flow assurance technology preventing pipelines from hydrate blockages becomes increasingly significant. However, the principle of hydrate inhibition is still poorly understood. Here, we examined natural hydrophobic amino acids as novel kinetic hydrate inhibitors (KHIs), and investigated hydrate inhibition phenomena by using them as a model system. Amino acids with lower hydrophobicity were found to be better KHIs to delay nucleation and retard growth, working by disrupting the water hydrogen bond network, while those with higher hydrophobicity strengthened the local water structure. It was found that perturbation of the water structure around KHIs plays a critical role in hydrate inhibition. This suggestion of a new class of KHIs will aid development of KHIs with enhanced biodegradability, and the present findings will accelerate the improved control of hydrate formation for natural gas exploitation and the utilization of hydrates as next-generation gas capture media.

Natural gas hydrates are solid hydrogen-bonded water crystals containing small molecular gases. The amount of natural gas stored as hydrates in permafrost and ocean sediments is twice that of all other fossil fuels combined. However, hydrate blockages also hinder oil/gas pipeline transportation, and, despite their huge potential as energy sources, our insufficient understanding of hydrates has limited their extraction. Here, we report how the presence of amino acids in water induces changes in its structure and thus interrupts the formation of methane and natural gas hydrates. The perturbation of the structure of water by amino acids and the resulting selective inhibition of hydrate cage formation were observed directly. A strong correlation was found between the inhibition efficiencies of amino acids and their physicochemical properties, which demonstrates the importance of their direct interactions with water and the resulting dissolution environment. The inhibition of methane and natural gas hydrate formation by amino acids has the potential to be highly beneficial in practical applications such as hydrate exploitation, oil/gas transportation, and flow assurance. Further, the interactions between amino acids and water are essential to the equilibria and dynamics of many physical, chemical, biological, and environmental processes.

The motivation for this work was the potential of hydrophobic amino acids such as glycine, l-alanine, and l-valine to be applied as thermodynamic hydrate inhibitors (THIs). To confirm their capabilities in inhibiting the formation of gas hydrates, three-phase (liquid-hydrate-vapor) equilibrium conditions for carbon dioxide hydrate formation in the presence of 0.1-3.0 mol % amino acid solutions were determined in the range of 273.05-281.45 K and 14.1-35.2 bar. From quantitative analyses, the inhibiting effects of the amino acids (on a mole concentration basis) decreased in the following order: l-valine > l-alanine > glycine. The application of amino acids as THIs has several potential advantages over conventional methods. First, the environmentally friendly nature of amino acids as compared to conventional inhibitors means that damage to ecological systems and the environment could be minimized. Second, the loss of amino acids in recovery process would be considerably reduced because amino acids are nonvolatile. Third, amino acids have great potential as a model system in which to investigate the inhibition mechanism on the molecular level, since the structure and chemical properties of amino acids are well understood.

Natural gas hydrates are icy crystalline materials that contain hydrocarbons, which are the primary energy source for this civilization. The abundance of naturally occurring gas hydrates leads to a growing interest in exploitation. Despite their potential as energy resources and in industrial applications, there is insufficient understanding of hydrate kinetics, which hinders the utilization of these invaluable resources. Perturbation of liquid water structure by solutes has been proposed to be a key process in hydrate inhibition, but this hypothesis remains unproven. Here, we report the direct observation of the perturbation of the liquid water structure induced by amino acids using polarized Raman spectroscopy, and its influence on gas hydrate nucleation and growth kinetics. Amino acids with hydrophilic and/or electrically charged side chains disrupted the water structure and thus provided effective hydrate inhibition. The strong correlation between the extent of perturbation by amino acids and their inhibition performance constitutes convincing evidence for the perturbation inhibition mechanism. The present findings bring the practical applications of gas hydrates significantly closer, and provide a new perspective on the freezing and melting phenomena of naturally occurring gas hydrates.

In Parts I and II, the Hu‐Lee‐Sum (HLS) correlation was developed and demonstrated to have an inherent generality and simplicity to predict structures I and II gas hydrates suppression temperature for both single and mixed salts systems. Utilization of thermodynamic hydrate inhibitors (THIs) is common practice in industry to prevent hydrate formation. Therefore, the HLS correlation is extended to predict hydrate suppression temperature with either single or mixed THIs, including any combination of inorganic salts and organic inhibitors. It is verified that hydrate equilibrium conditions with organic inhibitors also shows nearly independence of the water activity on temperature. In addition, additive contribution of salts and organic inhibitors to the water activity are used to determine the hydrate suppression temperature. A comprehensive comparison between the literature data and predicted results demonstrate the reliability of the HLS correlation for any combination of inorganic salts and organic inhibitors. © 2018 American Institute of Chemical Engineers AIChE J, 64: 4097–4109, 2018

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Deadlegs in oil and gas production systems often encounter hydrate plugs by deposition. Temperature is generally known to be an important variable in hydrate formation, but the effects in deadlegs are not exactly known. This study focuses on the effects of the header temperature on the hydrate deposition in gas-filled vertical deadlegs at constant wall temperature. All experiments are conducted with a methane/ethane gas mixture at constant pressure. The pipe wall temperature is kept constant while considering different header temperatures. The tests show that the header temperature has a significant impact in the hydrate deposit growth rate and distribution in the deadleg. It is also found that the hydrate deposit can, in turn, change the temperature field inside the pipe. The header temperature or the pipe temperature field can be used to estimate the hydrate distribution in the deadleg. Under the right conditions, hydrates can form a restriction in the deadleg and its location is usually close to the boundary of a hydrate-stable region. The location of the restriction can be correlated to the header temperature. At 80 °C, the location is estimated to be 15−18 ID, and at 30 °C, the location is estimated to be 9−12 ID. The results of this study contribute to the understanding of the hydrate deposition mechanism in deadlegs.

In the oil and gas industry, deadlegspipe sections without through-flowoften pose hydrate control challenges to gas and oil production systems. The hydrate challenges, if not properly managed, can cause severe consequences in terms of safety and cost for oil/gas production. This paper provides an overview of deadlegs in oil and gas production systems with some examples of typical challenges faced in the oil industry. Two different types of vertical deadleg experimental systems have been developed to acquire a better understanding of hydrate risks in gas-dominated deadlegs. These systems offer valuable quantitative information on hydrate deposit, such as thickness, porosity, morphology, growth rate, distribution, temperature profile, and amount of water and/or gas consumed as a factor of time in the deadleg system.