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Injecting carbon dioxide to extract methane from methane hydrate deposits?
27-10-2003: Two of the most pressing problems of our time are the ever-dwindling fossil
fuels and the threatening climate change resulting from the increasing release
of carbon dioxide. A means to simultaneously remove carbon dioxide while also
producing methane would truly resemble the Philosopher's Stone. Is this a
utopian vision or reality? A team of Canadians and Koreans, headed by John A.
Ripmeester, has now verified the practicability of such potential future
technologies.
What it's all about? Some time ago, huge deposits of "combustible ice" were
found at the edges of the continental plates and in regions of perpetual ice.
The substance in question is methane hydrate, which was formed from methane and
water by the decomposition of microorganisms at low temperatures and high
pressure. It is attractive to think we could release the methane in these
reservoirs in order to exploit the relatively clean-burning gas as a future
energy source. However, extracting the methane isn't exactly trivial, since it
isn't stored in a "gas bubble", but rather as a solid, locked into an ice-like
structure. It has been theorized that we could force the methane out of its icy
prison-by forcing in carbon dioxide, which could thus be elegantly stored away
for the long term. But can this theory be put into practice?
Two things have to be right in order for a reaction to work: The thermodynamics
determine the equilibrium that is established between reactants and products and
thus give us information about the maximum possible yield. The kinetics
determine how long it will take to reach this equilibrium. Calculations led
Ripmeester and his colleagues to the realization that both of these parameters
are favorable for this particular venture. Laboratory experiments then also
demonstrated that carbon dioxide could extract gaseous methane from methane
hydrate. However, the quantity of methane obtained was significantly lower than
the kinetic and thermodynamic considerations indicated. One reason for this
could be the initial exchange of the gases on the surface of the hydrate
particles. Inside the crystals, islands of methane hydrate remain, surrounded by
a mixed hydrate. Further exchange is then no longer possible. It is no wonder
that factors such as the distribution of methane hydrate in the sediment and
especially the size of the crystals within a specific deposit have a large
influence on the yield, deciding the success or failure of the technology.
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