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Measurements of methane hydrate equilibrium in systems inhibited with NaCl and methanol
Institution:1. School of Urban and Environmental Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 689-798, Republic of Korea;2. Petroleum & Marine Resources Division, Korea Institute of Geoscience & Mineral Resources (KIGAM), Daejeon 305-350, Republic of Korea;3. Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 305-701, Republic of Korea;1. National Energy Technological Laboratory, Morgantown, WV 26506, United States;2. Department of Chemical Engineering, West Virginia University, Morgantown, WV 26506, United States;1. Hydrates Energy Innovation Laboratory, Chemical & Biological Engineering Department, Colorado School of Mines, Golden, CO 80401, USA;2. Wood Group, Flow Assurance Department, Houston, TX 77084, USA;3. ConocoPhillips, Production Assurance, Bartlesville, OK 74004, USA;4. Department of Chemical Engineering, Pohang University of Science & Technology, Cheongam-Ro, Nam-Gu, Pohang, Gyeongbuk 37673, Republic of Korea;1. School of Urban and Environmental Engineering, Ulsan National Institute of Science and Technology, Ulsan 689-798, Republic of Korea;2. Offshore Plant Resources R&D Center, Korea Institute of Industrial Technology, Busan 618-230, Republic of Korea
Abstract:Natural gas hydrates are ice-like inclusion compounds that form at high pressures and low temperatures in the presence of water and light hydrocarbons. Hydrate formation conditions are favorable in gas and oil pipelines, and their formation threatens gas and oil production. Thermodynamic hydrate inhibitors (THIs) are chemicals (e.g., methanol, monoethylene glycol) deployed in gas pipelines to depress the equilibrium temperature required for hydrate formation. This work presents a novel application of a stepwise differential scanning calorimeter (DSC) measurement to accurately determine the methane hydrate phase boundary in the presence of THIs. The scheme is first validated on a model (ice + salt water) system, and then generalized to measure hydrate equilibrium temperatures for pure systems and 0.035 mass fraction NaCl solutions diluted to 0, 0.05, 0.10, and 0.20 mass fraction methanol. The hydrate equilibrium temperatures are measured at methane pressures from (7.0 to 20.0) MPa. The measured equilibrium temperatures are compared to values computed by the predictive hydrate equilibrium tool CSMGem.
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