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通过原位低温 X 射线粉末衍射研究甲烷水合物分解动力学。

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

机构信息

Department of Materials Science and Engineering, University of Tennessee, 1508 Middle Dr., Knoxville, Tennessee 37996-2100, USA.

出版信息

J Phys Chem A. 2013 May 2;117(17):3593-8. doi: 10.1021/jp4020178. Epub 2013 Apr 16.

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.

摘要

天然气水合物在环境压力和低于冰熔点的温度下已知分解速度较慢。当水合物放热分解时,气体被释放出来,笼形水合物中的水转化为冰。基于三种名义上相似的甲烷水合物样品分解的结果,通过原位低温 X 射线粉末衍射研究了总分解范围 140-260 K 内两个区域 180-200 和 230-260 K 的动力学。通过阿仑尼乌斯图确定了每个区域内甲烷水合物形成冰的反应动力学速率常数 k(a)和反应机制 n,通过阿伏伽德罗模型确定了活化能 E(a)。通过数据确定的 180-200 K 下的 E(a)为 42 kJ/mol,230-260 K 下的 E(a)为 22 kJ/mol。低温范围内较高的 E(a)归因于两个区域之间冰的微观结构的差异。

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