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Analysis of adsorbate-adsorbate and adsorbate-adsorbent interactions to decode isosteric heats of gas adsorption

journal contribution
posted on 14.01.2016, 13:15 by S. Hadi Madani, Saeid Sedghi, Mark Biggs, Phillip Pendleton
A qualitative interpretation is proposed to interpret isosteric heats of adsorption by considering contributions from three general classes of interaction energy: fluid–fluid heat, fluid–solid heat, and fluid—high-energy site (HES) heat. Multiple temperature adsorption isotherms are defined for nitrogen, T=(75, 77, 79) K, argon at T=(85, 87, 89) K, and for water and methanol at T=(278, 288, 298) K on a well-characterized polymer-based, activated carbon. Nitrogen and argon are subjected to isosteric heat analyses; their zero filling isosteric heats of adsorption are consistent with slit-pore, adsorption energy enhancement modelling. Water adsorbs entirely via specific interactions, offering decreasing isosteric heat at low pore filling followed by a constant heat slightly in excess of water condensation enthalpy, demonstrating the effects of micropores. Methanol offers both specific adsorption via the alcohol group and non-specific interactions via its methyl group; the isosteric heat increases at low pore filling, indicating the predominance of non-specific interactions.

Funding

This paper was supported by the Australian Research Council discovery program (DP110101293).

History

School

  • Science

Department

  • Chemistry

Published in

ChemPhysChem

Pages

n/a - n/a

Citation

MADANI, S.H. ...et al., 2015. Analysis of adsorbate-adsorbate and adsorbate-adsorbent interactions to decode isosteric heats of gas adsorption. ChemPhysChem, 16(18), pp. 3797–3805.

Publisher

© Wiley-VCH Verlag

Version

VoR (Version of Record)

Publisher statement

This work is made available according to the conditions of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) licence. Full details of this licence are available at: https://creativecommons.org/licenses/by-nc-nd/4.0/

Publication date

2015

Notes

This paper is in closed access.

ISSN

1439-4235

Language

en

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