Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

Preliminary evaluation of new polymer matrix for solid-phase extraction of nonylphenol from water samples

Guerreiroa, Antonio ; Soares, Ana ; Piletska, Elena ; Mattiasson, Bo LU and Piletsky, Sergey (2008) In Analytica Chimica Acta 612(1). p.99-104
Abstract
Molecularly imprinted (MIP) and blank polymers with affinity for nonylphenol were designed using computational modelling. Chromatographic tests demonstrated higher affinity of imprinted polymers towards the template nonylphenol as compared with blank polymers. The performance of both polymers in solid-phase extraction was however very similar. Both blank and imprinted polymers appeared to be suitable for the removal and pre-concentration of nonylphenol from contaminated water samples with 99% efficiency of the recovery. The commercial resins PH(EC) (Biotage) and C18 (Varian) tested in the same conditions used for comparative purposes had recovery rate < 84%. The polymer capacity for nonylphenol was 231 mg g(-1) for blank and 228 mg... (More)
Molecularly imprinted (MIP) and blank polymers with affinity for nonylphenol were designed using computational modelling. Chromatographic tests demonstrated higher affinity of imprinted polymers towards the template nonylphenol as compared with blank polymers. The performance of both polymers in solid-phase extraction was however very similar. Both blank and imprinted polymers appeared to be suitable for the removal and pre-concentration of nonylphenol from contaminated water samples with 99% efficiency of the recovery. The commercial resins PH(EC) (Biotage) and C18 (Varian) tested in the same conditions used for comparative purposes had recovery rate < 84%. The polymer capacity for nonylphenol was 231 mg g(-1) for blank and 228 mg g(-1) for MIR The synthesised materials can have significance for sample pre- concentration and environmental analysis of this class of compounds. (Less)
Please use this url to cite or link to this publication:
author
; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
molecularly imprinted polymer, nonylphenol, computational design
in
Analytica Chimica Acta
volume
612
issue
1
pages
99 - 104
publisher
Elsevier
external identifiers
  • wos:000254673000012
  • scopus:40249104568
  • pmid:18331863
ISSN
1873-4324
DOI
10.1016/j.aca.2008.02.010
language
English
LU publication?
yes
id
49ad7d88-09e0-42a5-a308-6f2311ca4f8a (old id 1182741)
date added to LUP
2016-04-01 14:43:44
date last changed
2022-01-28 02:14:41
@article{49ad7d88-09e0-42a5-a308-6f2311ca4f8a,
  abstract     = {{Molecularly imprinted (MIP) and blank polymers with affinity for nonylphenol were designed using computational modelling. Chromatographic tests demonstrated higher affinity of imprinted polymers towards the template nonylphenol as compared with blank polymers. The performance of both polymers in solid-phase extraction was however very similar. Both blank and imprinted polymers appeared to be suitable for the removal and pre-concentration of nonylphenol from contaminated water samples with 99% efficiency of the recovery. The commercial resins PH(EC) (Biotage) and C18 (Varian) tested in the same conditions used for comparative purposes had recovery rate &lt; 84%. The polymer capacity for nonylphenol was 231 mg g(-1) for blank and 228 mg g(-1) for MIR The synthesised materials can have significance for sample pre- concentration and environmental analysis of this class of compounds.}},
  author       = {{Guerreiroa, Antonio and Soares, Ana and Piletska, Elena and Mattiasson, Bo and Piletsky, Sergey}},
  issn         = {{1873-4324}},
  keywords     = {{molecularly imprinted polymer; nonylphenol; computational design}},
  language     = {{eng}},
  number       = {{1}},
  pages        = {{99--104}},
  publisher    = {{Elsevier}},
  series       = {{Analytica Chimica Acta}},
  title        = {{Preliminary evaluation of new polymer matrix for solid-phase extraction of nonylphenol from water samples}},
  url          = {{http://dx.doi.org/10.1016/j.aca.2008.02.010}},
  doi          = {{10.1016/j.aca.2008.02.010}},
  volume       = {{612}},
  year         = {{2008}},
}