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 AbstractA novel chemical inducer of Streptococcus quorum sensing acts by inhibiting the pheromone-degrading endopeptidase PepO    Next AbstractDetection of soil pollution by hydrocarbons using headspace-mass spectrometry and identification of compounds by headspace-fast gas chromatography-mass spectrometry »

Anal Chem


Title:Calibration transfer for solving the signal instability in quantitative headspace-mass spectrometry
Author(s):Perez Pavon JL; del Nogal Sanchez M; Garcia Pinto C; Fernandez Laespada ME; Moreno Cordero B;
Address:"Departamento de Quimica Analitica, Nutricion y Bromatologaia, Facultad de Ciencias Quimicas, Universidad de Salamanca, 37008 Salamanca, Spain. jlpp@usa1.es"
Journal Title:Anal Chem
Year:2003
Volume:75
Issue:22
Page Number:6361 - 6367
DOI: 10.1021/ac034543d
ISSN/ISBN:0003-2700 (Print) 0003-2700 (Linking)
Abstract:"It is reported that calibration transfer is able to compensate the variations in sensitivity in direct coupling of a headspace sampler to a mass spectrometer when used for quantification purposes using multivariate calibration techniques. This strategy of signal stability compensation allows the use of models constructed from large calibration standard sets without having to repeat their measurement even though variations occur in sensitivity, which may or may not be constant along the mass range. This technique offers advantages over the use of internal standards in this methodology and only requires the measurement of a small number of transfer samples with each set of unknown samples. The results obtained in the determination of six volatile organic compounds-benzene, toluene, ethylbenzene, and m-xylene (BTEX), methyl tert-butyl ether (MTBE), and mesitylene-are reported. To obtain an appropriate calibration set, a Plackett-Burman design with five levels of concentration for each component was employed. A PLS multivariate calibration model was constructed with a group of 25 samples. For selection of the optimum number of principal components, an external validation set (5 samples) was used and the prediction capacity of this set was checked with an additional group of samples that had not been used either in the construction or in the validation of the model. The results obtained can be considered highly satisfactory, and the methodology was successfully tested with natural matrixes (river and tap water)"
Keywords:
Notes:"PubMed-not-MEDLINEPerez Pavon, Jose Luis del Nogal Sanchez, Miguel Garcia Pinto, Carmelo Fernandez Laespada, M Esther Moreno Cordero, Bernardo eng 2003/11/18 Anal Chem. 2003 Nov 15; 75(22):6361-7. doi: 10.1021/ac034543d"

 
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 26-12-2024