Abstract
Particle size distribution measurements were performed during the growth stage of methane hydrate formation in a semi-batch stirred tank crystallizer. Experiments were carried out at temperatures between 275.1 and 279.2 K and pressures ranging from 3873 to 5593 kPa. The reaction rate constant of methane hydrate formation was determined using the model of Bergeron and Servio (AIChE J 2008;54:2964). The experimental reaction rate constant was found to increase with temperature, following an Arrhenius-type relationship, from 8.3 × 10 −8 m/s to 6.15 × 10 −7 m/s over the 4° range investigated, resulting in an activation energy of 323 kJ/mol. An increase in pressure of approximately 600 kPa did not have any effect on the reaction rate constant. Population balances, based on the measured critical nuclei diameter and that predicted by homogeneous nucleation theory, were also used for comparison purposes. The initial number of hydrate particles was calculated using the mole fraction of methane in the bulk liquid phase and compared to that predicted by an energy balance.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.