Published April 30, 2017 | Version v1
Journal article

Montmorillonite-supported Pd0, Fe0, Cu0 and Ag0 nanoparticles: Properties and affinity towards CO2

  • 1. Research unit: Environment, Catalyzes and Process Analysis, ENIG University of Gabes (Tunisia)
  • 2. Nanoqam, Department of Chemistry, University of Quebec at Montreal, QC, H3C 3P8 Canada (Canada)

Description

Highlights: • Purification and modification of montmorillonite. • Dispersion and immobilization of metallic nanoparticles within NaMt layers. • Changes of the distance between the minerals clay layers. • Applications of NaMt-M-NPs adsorbents for adsorption of CO2. - Abstract: This study reports the carbon dioxide (CO2) adsorption on montmorillonite (NaMt) incorporating Cu0, Fe0, Pd0 and Ag0 as metallic nanoparticles (MNPs). The changes in structural, textural, morphological and adsorption properties of the resulting materials (NaMt-MNPs) were investigated. Electron microscopy and X-ray diffraction showed that dispersion of fine MNPs occurs mainly within the interlayer space of NaMt, producing a slight structure expansion. This was accompanied by a visible enhancement of the affinity towards CO2, as supported by thermal programmed desorption measurements. NaMt-MNPs displayed high CO2 retention capacity (CRC) of ca. 657 μmol/g for NaMt-Cu as compared to NaMt. This was explained in terms of increased number of available adsorption sites due to enlarged interlayer spaces caused by MNP insertion. The differences in CO2 adsorption capacities clearly demonstrate the key role of MNPs in improving the surface properties and adsorption capacity. The results reported herein open new prospects for clay supported metal nanoparticles as efficient adsorbents for CO2.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apsusc.2017.01.004

Additional details

Identifiers

DOI
10.1016/j.apsusc.2017.01.004;
PII
S0169-4332(17)30005-3;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
402
Journal Page Range
p. 314-322
ISSN
0169-4332
CODEN
ASUSEE

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.