Literature DB >> 23557375

Kinetics of methane hydrate decomposition studied via in situ low temperature X-ray powder diffraction.

S Michelle Everett1, Claudia J Rawn, David J Keffer, Derek L Mull, E Andrew Payzant, Tommy J Phelps.   

Abstract

Gas hydrate is known to have a slowed decomposition rate at ambient pressure and temperatures below the melting point of ice. As hydrate exothermically decomposes, gas is released and water of the clathrate cages transforms into ice. Based on results from the decomposition of three nominally similar methane hydrate samples, the kinetics of two regions, 180-200 and 230-260 K, within the overall decomposition range 140-260 K, were studied by in situ low temperature X-ray powder diffraction. The kinetic rate constants, k(a), and the reaction mechanisms, n, for ice formation from methane hydrate were determined by the Avrami model within each region, and activation energies, E(a), were determined by the Arrhenius plot. E(a) determined from the data for 180-200 K was 42 kJ/mol and for 230-260 K was 22 kJ/mol. The higher E(a) in the colder temperature range was attributed to a difference in the microstructure of ice between the two regions.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23557375     DOI: 10.1021/jp4020178

Source DB:  PubMed          Journal:  J Phys Chem A        ISSN: 1089-5639            Impact factor:   2.781


  1 in total

1.  Origin of Self-preservation Effect for Hydrate Decomposition: Coupling of Mass and Heat Transfer Resistances.

Authors:  Dongsheng Bai; Diwei Zhang; Xianren Zhang; Guangjin Chen
Journal:  Sci Rep       Date:  2015-10-01       Impact factor: 4.379

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.