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« Previous AbstractPolydimethylsiloxane-based permeation passive air sampler. Part II: Effect of temperature and humidity on the calibration constants    Next AbstractPolarization of yeast cells in spatial gradients of alpha mating factor »

J Chromatogr A


Title:Polydimethylsiloxane-based permeation passive air sampler. Part I: Calibration constants and their relation to retention indices of the analytes
Author(s):Seethapathy S; Gorecki T;
Address:"Department of Chemistry, University of Waterloo, 200 University Avenue West, Waterloo, Ontario, Canada N2L3G1"
Journal Title:J Chromatogr A
Year:2011
Volume:20101109
Issue:1
Page Number:143 - 155
DOI: 10.1016/j.chroma.2010.11.003
ISSN/ISBN:1873-3778 (Electronic) 0021-9673 (Linking)
Abstract:"A simple and cost effective permeation passive sampler equipped with a polydimethylsiloxane (PDMS) membrane was designed for the determination of time-weighted average (TWA) concentrations of volatile organic compounds (VOCs) in air. Permeation passive samplers have significant advantages over diffusive passive samplers, including insensitivity to moisture and high face velocities of air across the surface of the sampler. Calibration constants of the sampler towards 41 analytes belonging to alkane, aromatic hydrocarbon, chlorinated hydrocarbon, ester and alcohol groups were determined. The calibration constants allowed for the determination of the permeability of PDMS towards the selected analytes. They ranged from 0.026 cm(2) min(-)(1) for 1,1-dichloroethylene to 0.605 cm(2) min(-)(1) for n-octanol. Further, the mechanism of analyte transport across PDMS membranes allowed for the calibration constants of the sampler to be estimated from the linear temperature programmed retention indices (LTPRI) of the analytes, determined using GC columns coated with pure PDMS stationary phases. Statistical analysis using Student's t test indicated that there was no significant difference at the 95% probability level between the experimentally obtained calibration constants and those estimated using LTPRI for most analyte groups studied. This correlation allows the estimation of the calibration constants of compounds not known to be present at the time of sampler deployment, which makes it possible to determine parameters like total petroleum hydrocarbons in the vapor phase"
Keywords:"Air/*analysis Algorithms Calibration Chromatography, Gas/instrumentation/*methods Dimethylpolysiloxanes/*chemistry Environmental Monitoring/methods Hydrocarbons/chemistry Linear Models *Models, Theoretical Permeability Petroleum Temperature Volatile Organ;"
Notes:"MedlineSeethapathy, Suresh Gorecki, Tadeusz eng Research Support, Non-U.S. Gov't Netherlands 2010/11/30 J Chromatogr A. 2011 Jan 7; 1218(1):143-55. doi: 10.1016/j.chroma.2010.11.003. Epub 2010 Nov 9"

 
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