Published July 2010 | Version v1
Journal article

Adsorption properties of carbonized polyacrylonitrile deposited on γ-alumina and silica gel by precipitation polymerization

  • 1. Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Krakow (Poland)
  • 2. Institute of Geological Sciences, Jagiellonian University, Oleandry 2a, 30-063 Krakow (Poland)

Description

The precipitation polymerization method was used for the deposition of various contents of polyacrylonitrile on two oxide-type supports (γ-alumina and silica gel). The synthesized materials were characterized by thermal analysis performed in inert and oxidizing atmospheres. The mechanism of polyacrylonitrile decomposition was proposed. In order to gain effective adsorbents of volatile organic compounds the polyacrylonitrile/support composites were carbonized at elevated temperatures. The texture and morphology of the calcined materials were examined by low-temperature sorption of N2 and scanning electron microscopy, respectively. An influence of thermal treatment conditions and carbonaceous species loading on adsorption capacity of methyl-ethyl ketone vapour was also determined. Attenuated total reflection Fourier transform infrared spectroscopy measurements revealed that the ladder-type polyacrylonitrile species formed above 250 oC and stable up to about 350-400 oC are the most effective sites for methyl-ethyl ketone sorption. The carbonaceous species dispersion was found to be an additional factor influencing the adsorption capacity of the carbonized polyacrylonitrile/support composites.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.materresbull.2010.03.017

Additional details

Identifiers

DOI
10.1016/j.materresbull.2010.03.017;
PII
S0025-5408(10)00100-5;

Publishing Information

Journal Title
Materials Research Bulletin
Journal Volume
45
Journal Issue
7
Journal Page Range
p. 787-793
ISSN
0025-5408
CODEN
MRBUAC

Optional Information

Copyright
Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.