Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractIntrafloral patterns of color and scent in Capparis spinosa L. and the ghosts of its selection past    Next AbstractMethanol utilizers of the rhizosphere and phyllosphere of a common grass and forb host species »

Talanta


Title:Internally heated membrane interfaced to a gas chromatography flame ionization detector
Author(s):Kanu AB; Thomas CL;
Address:"Department of Chemistry, Winston-Salem State University, Winston-Salem, NC 27110, USA. kanuabb@wssu.edu"
Journal Title:Talanta
Year:2013
Volume:20130313
Issue:
Page Number:215 - 223
DOI: 10.1016/j.talanta.2013.03.011
ISSN/ISBN:1873-3573 (Electronic) 0039-9140 (Linking)
Abstract:"Volatile Organic Compounds (VOCs) mixtures in aqueous solutions have been investigated using a simple and efficient all-in-one on-line sampling, isolation, enrichment and pre-concentration internally heated membrane connected to a gas chromatography flame ionization detector (GC-FID). In our previous study with the internally heated membrane, no GC column was used in the instrument. In this new study, we introduce a GC column in the instrument design and this makes it possible for mixtures to be investigated. This new experimental design enabled high resolution separation of analyte mixtures capable of being adsorbed, diffused, and desorbed from the device for detection with an FID. With the new design we present data from investigation of competitive adsorption effects on the membrane. The data showed that analyte adsorption and diffusion onto the membrane can be affected when mixtures of analytes are introduced. The application of multiple linear regressions approach to the data enabled us to correct for the problem of competitive adsorption. Analyte adsorption and diffusion was affected by the diffusion coefficients of the analytes; the higher the diffusion coefficient the better the extraction from the membrane. Increasing the sampling time from 1 to 4 min increases the response by 77%. The sampling time responses were linear up to 4 min sampling time. Above 4 min sampling time, the data deviate from linearity. The effect of adding salt to standards has no effect on analyte absorption onto the membrane. The detection limits for key VOCs studied with an internal standard calibration ranged from 0.2 to 194 ng cm(-3)"
Keywords:"Adsorption Calibration Chromatography, Gas/*instrumentation/*methods Diffusion Flame Ionization/instrumentation/methods Heating/*methods Hot Temperature Reproducibility of Results Time Factors Volatile Organic Compounds/*analysis/chemistry;"
Notes:"MedlineKanu, A Bakarr Thomas, C L P eng Research Support, Non-U.S. Gov't Netherlands 2013/04/30 Talanta. 2013 Jul 15; 111:215-23. doi: 10.1016/j.talanta.2013.03.011. Epub 2013 Mar 13"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 04-12-2024