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界面机制控制环戊烷笼型水合物的附着/内聚。

Interfacial mechanisms governing cyclopentane clathrate hydrate adhesion/cohesion.

机构信息

Center for Hydrate Research, Dept. of Chemical Engineering, Colorado School of Mines, Golden, Colorado 80401, USA.

出版信息

Phys Chem Chem Phys. 2011 Nov 28;13(44):19796-806. doi: 10.1039/c1cp21907c. Epub 2011 Oct 10.

Abstract

The present work uses a micromechanical force apparatus to directly measure cyclopentane clathrate hydrate cohesive force and hydrate-steel adhesive force, as a function of contact time, contact force and temperature. We present a hydrate interparticle force model, which includes capillary and sintering contributions and is based on fundamental interparticle force theories. In this process, we estimate the cyclopentane hydrate tensile strength to be approximately 0.91 MPa. This hydrate interparticle force model also predicts the effect of temperature on hydrate particle cohesion force. Finally, we present the first direct measurements of hydrate cohesive force in the gas phase to be 9.1 ± 2.1 mN/m at approximately 3 °C (as opposed to 4.3 ± 0.4 mN/m in liquid cyclopentane).

摘要

本工作使用微机械力装置直接测量环戊烷笼形水合物内聚强度和水合物-钢黏附力,作为接触时间、接触力和温度的函数。我们提出了一个包含毛细和烧结贡献的水合物颗粒间力模型,该模型基于基本的颗粒间力理论。在这个过程中,我们估计环戊烷水合物的拉伸强度约为 0.91 MPa。该水合物颗粒间力模型还预测了温度对水合物颗粒内聚强度的影响。最后,我们首次直接测量到在大约 3°C 时气相中水合物的内聚强度约为 9.1 ± 2.1 mN/m(而在液态环戊烷中为 4.3 ± 0.4 mN/m)。

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