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基于晶种模拟的实验条件下甲烷水合物形成的均相成核速率

Homogeneous nucleation rate of methane hydrate formation under experimental conditions from seeding simulations.

作者信息

Grabowska J, Blazquez S, Sanz E, Noya E G, Zeron I M, Algaba J, Miguez J M, Blas F J, Vega C

机构信息

Dpto. Química Física I, Fac. Ciencias Químicas, Universidad Complutense de Madrid, 28040 Madrid, Spain.

Instituto de Química Física Rocasolano, CSIC, C/ Serrano 119, 28006 Madrid, Spain.

出版信息

J Chem Phys. 2023 Mar 21;158(11):114505. doi: 10.1063/5.0132681.

DOI:10.1063/5.0132681
PMID:36948790
Abstract

In this work, we shall estimate via computer simulations the homogeneous nucleation rate for the methane hydrate at 400 bars for a supercooling of about 35 K. The TIP4P/ICE model and a Lennard-Jones center were used for water and methane, respectively. To estimate the nucleation rate, the seeding technique was employed. Clusters of the methane hydrate of different sizes were inserted into the aqueous phase of a two-phase gas-liquid equilibrium system at 260 K and 400 bars. Using these systems, we determined the size at which the cluster of the hydrate is critical (i.e., it has 50% probability of either growing or melting). Since nucleation rates estimated from the seeding technique are sensitive to the choice of the order parameter used to determine the size of the cluster of the solid, we considered several possibilities. We performed brute force simulations of an aqueous solution of methane in water in which the concentration of methane was several times higher than the equilibrium concentration (i.e., the solution was supersaturated). From brute force runs, we infer the value of the nucleation rate for this system rigorously. Subsequently, seeding runs were carried out for this system, and it was found that only two of the considered order parameters were able to reproduce the value of the nucleation rate obtained from brute force simulations. By using these two order parameters, we estimated the nucleation rate under experimental conditions (400 bars and 260 K) to be of the order of log (J/(m s)) = -7(5).

摘要

在这项工作中,我们将通过计算机模拟估算在400巴压力和约35K过冷度下甲烷水合物的均相成核速率。水和甲烷分别采用TIP4P/ICE模型和Lennard-Jones中心。为了估算成核速率,采用了晶种技术。将不同尺寸的甲烷水合物簇插入到260K和400巴压力下的气-液两相平衡系统的水相中。利用这些系统,我们确定了水合物簇成为临界状态的尺寸(即其生长或融化的概率为50%)。由于从晶种技术估算的成核速率对用于确定固体簇尺寸的序参量的选择很敏感,我们考虑了几种可能性。我们对水中甲烷的水溶液进行了蛮力模拟,其中甲烷浓度比平衡浓度高几倍(即溶液是过饱和的)。从蛮力模拟中,我们严格推断出该系统的成核速率值。随后,对该系统进行了晶种模拟,发现只有两个考虑的序参量能够重现从蛮力模拟中获得的成核速率值。通过使用这两个序参量,我们估算出在实验条件(400巴和260K)下的成核速率约为log (J/(m s)) = -7(5)。

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