276609 Remarkable CO2 Uptakes in MOFs Whilst in the Presence of Water Vapor

Tuesday, October 30, 2012: 12:30 PM
405 (Convention Center )
Philip L. Llewellyn, Estelle Lenoir and Christelle Vagner, MADIREL (UMR7246), Aix-Marseille Univ. / CNRS, Marseille, France

The search for solutions for economic CO2capture from flue gases is ever continuing. Capture using physical adsorption could be viable as long as the right adsorbent is found and indeed amine functionalized materials could be of interest.

Our group is interested in the initial evaluation of various adsorbent materials for a number of different processes. In this respect, Metal Organic Frameworks are a particularly interesting family of materials due to the possibility to vary the metal centre and/or organic linker to give a huge variety of physical and chemical properties. The problem here is that with such a wide variety of materials to hand, which are of interest for CO2capture ?

Indeed, the capture of CO2 from flue gases poses a number of problems in terms of low CO2 concentration (below 20%), low total pressure (1 bar), and the eventual presence of water. Indeed, whilst many MOFs seem to be unstable in the presence of water, some studies suggest that CO2capture in moderate humidity’s enhance CO2 uptake. This is in contrast with zeolites and activated carbons where water has a detrimental effect.

Our work will show several cases where water plays a determining role during CO2uptakes in various MOFs. Uptakes are measured using chromatography and simultaneously we are able to directly measure the heats using microcalorimetry.

Two separate cases will be considered : (1) mesoporous MOFs and (2) a bifunctional microporous MOF. These systems will be compared with a reference activated carbon and a zeolite. We show that in each case, considerable increases in CO2 capture can be attained in the presence of water vapor and we will give tentative explanations of the phenonena in play.


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See more of this Session: CO2 Capture by Adsorption-Adsorbents II
See more of this Group/Topical: Separations Division