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Carbon Management Technology Conference,
7-9 February 2012,
Orlando, Florida, USA
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Abstract
Because supercritical CO2, when injected onshore or in shallow water depths
offshore, is mobile and can, therefore, migrate through any conduits or
fractures, there is a need for proper physical trapping and also a necessity to
monitor the CO2 migration in the injected zone. In addition, public opinion,
government regulatory agencies and the lack of space for CO2 injection sites in
some of the largest CO2 emitting regions of the world encourage investigating
other alternatives such as CO2 sequestration in deepwater sub-seabed
formations.
Furthermore, at the high pressures and low temperatures reigning in deepwater
sediments where water depths are greater than 9,000 feet (≈2,750 meters),
scientists have proposed that the CO2 should become denser than seawater and
therefore would remain buoyantly trapped when liquid CO2 is injected within the
first few hundred feet of sediments even in the absence of geological seals and
traps. Besides, the bulk of the studies and technical papers concerning CO2
sequestration in deepwater sediments have focused on showing the potential and
the feasibility of the concept but very little has been published to
demonstrate the viability of the injection and long-term storage of CO2 in
deepwater sub-seabed formations.
This paper presents the results of several case studies located in the Gulf of
Mexico, the Pacific Ocean, the North Atlantic Ocean and the Sea of Japan. Large
time-scale reservoir simulations have been conducted for up to 250 years and
show that injected liquid CO2 can remain trapped in deepwater sediments under
certain sediment physical properties. Therefore, CO2 sequestration in deepwater
sediments provide another attractive technical solution when applied under
certain conditions of pressure, temperature, sediment type, thickness,
permeability and porosity notably for regions where there are few depleted oil
and gas fields available for storage or limited space accessible onshore.
Introduction
Human industrial activity through the consumption and flaring of fossil fuels
has resulted in the emission of nearly 30 billion tons of CO2 for the year 2010
according to the Energy Information Administration, seeing a constant increase
for CO2 atmospheric concentrations since the beginning of the industrial age.
Indeed, the CO2 concentrations have risen from 280 ppm in the 18th century to
about 390 ppm in 2010 and are forecasted to continue increasing at a rate of 2
ppm per year. Nonetheless, recent studies have estimated that oceans have
naturally sequestrated, by dissolving and mixing with deep waters, about 40% to
50% of the anthropogenic CO2 emitted during the same period of time. Therefore,
carbon dioxide capture and storage (CCS) techniques which involve capturing the
CO2 coming from the combustion of fossil fuels and some industrial processes;
then transporting and injecting this CO2 (either in a supercritical or liquid
state) in geological formations need to be investigated to ensure that these
methods could help reduce or mitigate CO2 emissions to the atmosphere.
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