Evaluating metal-organic frameworks for post-combustion carbon dioxide capture via temperature swing adsorption

Mason, Jarad A. ; Sumida, Kenji ; Herm, Zoey R. ; Krishna, Rajamani ; Long, Jeffrey R. (2011) Evaluating metal-organic frameworks for post-combustion carbon dioxide capture via temperature swing adsorption Energy & Environmental Science, 4 (8). pp. 3030-3040. ISSN 1754-5692

Full text not available from this repository.

Official URL: http://pubs.rsc.org/en/content/articlelanding/2011...

Related URL: http://dx.doi.org/10.1039/C1EE01720A

Abstract

Two representative metal-organic frameworks, Zn4O(BTB)2 (BTB3− = 1,3,5-benzenetribenzoate; MOF-177) and Mg2(dobdc) (dobdc4− = 1,4-dioxido-2,5-benzenedicarboxylate; Mg-MOF-74, CPO-27-Mg), are evaluated in detail for their potential use in post-combustion CO2 capture via temperature swing adsorption (TSA). Low-pressure single-component CO2 and N2 adsorption isotherms were measured every 10 °C from 20 to 200 °C, allowing the performance of each material to be analyzed precisely. In order to gain a more complete understanding of the separation phenomena and the thermodynamics of CO2 adsorption, the isotherms were analyzed using a variety of methods. With regard to the isosteric heat of CO2 adsorption, Mg2(dobdc) exhibits an abrupt drop at loadings approaching the saturation of the Mg2+ sites, which has significant implications for regeneration in different industrial applications. The CO2/N2 selectivities were calculated using ideal adsorbed solution theory (IAST) for MOF-177, Mg2(dobdc), and zeolite NaX, and working capacities were estimated using a simplified TSA model. Significantly, MOF-177 fails to exhibit a positive working capacity even at regeneration temperatures as high as 200 °C, while Mg2(dobdc) reaches a working capacity of 17.6 wt % at this temperature. Breakthrough simulations were also performed for the three materials, demonstrating the superior performance of Mg2(dobdc) over MOF-177 and zeolite NaX. These results show that the presence of strong CO2 adsorption sites is essential for a metal-organic framework to be of utility in post-combustion CO2 capture via a TSA process, and present a methodology for the evaluation of new metal-organic frameworks via analysis of single-component gas adsorption isotherms.

Item Type:Article
Source:Copyright of this article belongs to Royal Society of Chemistry.
ID Code:65316
Deposited On:17 Oct 2011 03:31
Last Modified:17 Oct 2011 03:31

Repository Staff Only: item control page