Thermodynamic characteristics of methane hydrate formation in high-pressure microcalorimeter under different reaction kinetics. (15th January 2023)

• Record Type: Journal Article
• Authors: Fu, Juan; Mo, Jia-Mei; Liu, Shi-Jun; Yi, Wen-Zhe; Yu, Yi-Song; Wu, Neng-You; Chen, Xiao-Li; Su, Qiu-Cheng; Li, Xiao-Sen
• Is Part Of: Fuel. Volume 332(2023)Part 1
• Publication Date: 2023-01-15
• Subjects: CH4 hydrate -- High-pressure microcalorimeter -- Kinetics -- Promoter -- Morphologies; Fuel -- Periodicals; Coal -- Periodicals; Coal; Fuel; Periodicals; 662.6
• DOI: 10.1016/j.fuel.2022.126072
• Languages: English
• ISSNs: 0016-2361

Abstract

Highlights: Promoter-CH4 hydrate formation in a high-pressure microcalorimeter is studied. The CH4 hydrate formation thermodynamic behavior depends greatly on the promoter. The hydrate structure has little effect on its formation thermodynamic behavior. Abstract: To understand the thermodynamic characteristics of CH4 hydrate formation in a high-pressure microcalorimeter under different reaction kinetics, five typical systems including CH4 -H2 O, CH4 -Tetrahydrofuran (THF)–H2 O, CH4 -Cyclopentane (CP)–H2 O, CH4 -Methyl cyclohexane (MCH)–H2 O, and CH4 - tert -Butyl methyl ether (TBME)–H2 O are adopted to conduct experiments in this work. The results show that their hydrate formation thermodynamic characteristics depend greatly on the promoter. For the CH4 -H2 O system, a hydrate crystals film will form quickly at the beginning of the reaction, hindering the mass transfer between gas and liquid, thereby presenting an extremely slow hydrate formation kinetics. After adding the water-soluble promoter that cannot form an oil phase, like THF, a rapid hydrate formation process is observed from the cooling stage. However, if the promoter can form an oil phase (CP, MCH, and TBME), regardless of whether the promoter is soluble in water, only a slow hydrate formation kinetics can be observed. This is because the oil phase can separate the water and gas phase, reducing their mass transfer efficiency, thereby restricting the hydrate growth. Interestingly, a rapid hydrate formation process can be obtained during their heating stage. These indicate that high driving force cannot always lead to a rapid hydrate formation kinetics. It is worth mentioning that a similar hydrate formation and dissociation behavior in high-pressure microcalorimeter is observed for water-insoluble promoters (CP, MCH), indicating the hydrate structure will not significantly affect their thermodynamic behavior except for the intensity of the peaks.