Funding
Agencies
National
Science Foundation
Collaborators
David Keith, CMU (EPP)
Publications
Stolaroff,
Joshuah K., Lowry, Gregory V., and Keith, David W. (2004). “CO2 extraction from ambient air using
alkali-metal hydroxide solutions derived from concrete waste and steel slag.”
In the Proceedings of the Fuel Chemistry
Division, 227th American Chemical Society National Meeting,
Stolaroff,
J. K., Lowry, G. V., Keith, D. (2006).
Experimental measurement of energy requirements for capturing CO2 from
ambient air in a pilot-scale system.
GHGT8, Eighth International Conference on Green House Gas Control
Technologies,
Abstract
Fossil fuel use in the 21st century will be
limited by environmental constraints.
The potential for carbon emissions is far larger than what the
atmosphere, the oceans or the biosphere could absorb without severe
environmental consequences. Within half
a century, the world must move roughly half way towards a zero net-CO2
energy system; emissions must be reduced by at least fifty percent of today’s
output by 2050. This could be
accomplished by gradually eliminating the use of fossil carbon in the energy
sector, or by capturing carbon dioxide, either at the source or from the air,
followed by its permanent and safe disposal (sequestration). While large-scale deployment of low carbon
technologies may be decades away, the enormous technological inertia of energy
infrastructures dictates that action to develop and test such technologies must
begin now if we are to achieve cost-effective solutions to the CO2
climate problem.
Research on industrial carbon management has focused on
capturing CO2 from large centralized facilities such as electric
power plants because of the higher CO2 concentrations emitted from
these sources. Recent published studies
by this team have demonstrated that it is possible to capture CO2
directly from the ambient air. The
feasibility and cost of large-scale CO2 capture from air by this
approach are, however, uncertain and somewhat controversial. The proposed CO2 capture scheme
uses a concentrated NaOH-based contactor to remove CO2 from ambient
air, then uses a commonly used chemical recovery method (Kraft process) to
regenerate the NaOH absorbing stream. CO2
captured by a calciner in the process is concentrated and made ready for
geologic storage. Despite considerable
industrial experience with these types of processes, it is far from clear what
an optimal contactor would look like and what the rate limiting steps are for a
contactor design involving strong alkaline solutions. Similarly, it is uncertain how to design and
operate a CO2 emission-free calciner capable of producing a
concentrated pressurized CO2 stream for sequestration. We propose to tackle these uncertainties
head-on through a suite of the scientific and engineering analyses and
laboratory experiments that will enable a robust assessment of the cost and feasibility
of large-scale air capture.

Greg Lowry Home | Dept. Civil & Env. Engr.
Last Modified: June 2003