Fluid Phase Equilibrium, Volume 231, Issue 2, Pages 176-187, 2005
BONNEFOY (O.), GRUY (F.) & HERRI (J.M.)
Ecole des Mines de Saint-Etienne, SPIN, 158 Cours Fauriel, 42023 Saint-Etienne Cedex 2, France.
The goal of this work is to quantify the Van der Waals interactions in systems
involving gas hydrates. Gas hydrates are crystalline com pounds that are often
encountered in oil and gas industry, where they pose problems (pipeline plugging,
. . . ) and represent opportunities (energy resources, gas transport, . . .
). We focus on methane hydrate, which is the most common one, and calculate
its Hamaker constant. Two methods are used and lead to results in good agreement.
The Hamaker, microscopic, approach gives a first estimate of the Hamaker constant
of 4.59×10−21 J for the hydrate-water-hydrate
system. The Lifshitz, macroscopic, method used in combination with the Kramers-Kronig
relationship gives a value of 8.25 × 10−21
J. The Hamaker constant is also computed for three phases systems (gas hydrate
clathrate and liquid water with ice,
dodecane, quartz, sapphire, teflon, metals). The interaction potential in different
geometrical configurations is then calculated by a hybrid method and various
cases of practical interest are studied.