TY - JOUR
T1 - Hyphenation of column liquid chromatography and Raman spectroscopy via a liquid-core waveguide: chemometrical elimination of spectral eluent background
AU - Dijkstra, R.J.
AU - Boelens, HA
AU - Westerhuis, J.A.
AU - Ariese, F.
AU - Brinkman, U.A.T.
AU - Gooijer, C.
PY - 2004
Y1 - 2004
N2 - In column liquid chromatography (LC) coupled to conventional Raman spectroscopy (RS) removal of the spectral background of the eluent is often demanding, because of the strong signals of the organic modifier. A new chemometrical method is proposed, called the eluent background subtraction (EBS) method, which can correct for small shape and intensity differences of the eluent spectra. The variations in the eluent spectra are modelled using principal component analysis (PCA). The PCA loading vectors are subsequently used for eluent background correction of the elution spectra of the analyte. The loading vectors are fitted under these spectra by an asymmetric least-squares method. This method was successfully applied under various experimental conditions and performed much better than conventional background correction methods. Analyte detectability was improved by (weighted) averaging of all elution spectra and smoothing via a p-spline function. © 2004 Elsevier B.V. All rights reserved.
AB - In column liquid chromatography (LC) coupled to conventional Raman spectroscopy (RS) removal of the spectral background of the eluent is often demanding, because of the strong signals of the organic modifier. A new chemometrical method is proposed, called the eluent background subtraction (EBS) method, which can correct for small shape and intensity differences of the eluent spectra. The variations in the eluent spectra are modelled using principal component analysis (PCA). The PCA loading vectors are subsequently used for eluent background correction of the elution spectra of the analyte. The loading vectors are fitted under these spectra by an asymmetric least-squares method. This method was successfully applied under various experimental conditions and performed much better than conventional background correction methods. Analyte detectability was improved by (weighted) averaging of all elution spectra and smoothing via a p-spline function. © 2004 Elsevier B.V. All rights reserved.
UR - https://www.scopus.com/pages/publications/3343010552
UR - https://www.scopus.com/inward/citedby.url?scp=3343010552&partnerID=8YFLogxK
U2 - 10.1016/j.aca.2004.06.008
DO - 10.1016/j.aca.2004.06.008
M3 - Article
SN - 0003-2670
VL - 519
SP - 129
EP - 136
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
IS - 2
ER -