Mixtures of methane and water under extreme conditions
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Authors
Pruteanu, Ciprian Gabriel
Abstract
The hydrophobic effect has been a topic of research for decades, not only due to
its importance as the primary building block of much of chemistry (it dictates
which solvent can dissolve which solutes) and biology (guiding protein binding
and gene expression) but also due to it being a fundamental physical process.
The commonly held opinion is that 'like dissolve like', implying polar substances
can readily mix with other polar substances, and similarly for apolar ones, but
polar and apolar would separate and tend to stay isolated from one another
(like oil in water). We have developed a quantitative imaging method that can
be used in tandem with Raman spectroscopy in order to investigate the effect
of high pressure on a model hydrophobic system - water and methane. Our
study revealed an unexpectedly large increase in the amount of methane that
can readily mix with water once a rather modest pressure has been applied
to the system. Thus, the solubility of CH4 in H2O starts abruptly increasing
at 1.3 GPa and reaches a maximum of 44(3) mole % at 2.1 GPa, showing no
pressure dependence upon further compression. We have tried to reproduce the
observed experimental behaviour using classical molecular dynamics simulations
deploying a range of widely used water potentials (SPC/E, TIP4P, TIP3P),
but unfortunately no quantitative or even qualitative agreement was reached
with experiments. Finally, in order to understand the atomic level changes that
enable this increased amount of methane to dissolve in water, we have performed
neutron scattering measurements along with EPSR (empirical potential structure
refinement) fits to the data in order to solve the structure of the fluid mixture.
These revealed a tendency towards maintaining the H-bond network present in
water and homogeneous mixing. Despite the network staying similar to the one
found in pure fluid water at milder pressures and temperatures (close to ambient
conditions), the H-bonds seem more disordered and show a greater variability in
their lengths.
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