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High order derivative to investigate the complexity of the near infrared spectra of aqueous solutions.

Authors :
Shao X
Cui X
Wang M
Cai W
Source :
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy [Spectrochim Acta A Mol Biomol Spectrosc] 2019 Apr 15; Vol. 213, pp. 83-89. Date of Electronic Publication: 2019 Jan 17.
Publication Year :
2019

Abstract

Derivative calculation is a powerful method for resolution enhancement in spectral analysis. A high order derivative method based on continuous wavelet transform (CWT) is discussed in the analysis of near infrared (NIR) spectra. The results for a simulated spectrum obtained from conventional numerical differentiation (NM), Fourier transform (FT), Savitzky-Golay (SG) and CWT method were compared. CWT method was found to be as efficient as FT and SG, but easier for high order derivative computation, and the fourth order derivative was proved to be a good choice for resolution enhancement as well as reduction of noise and sidelobe effects. For the NIR spectra of water-ethanol mixtures, the complexity of the spectra can be observed from the fourth derivative, including the spectral features of OH and CH with various intermolecular interactions. Fitting the derivative spectra of the mixtures by those of pure water and ethanol, the obtained coefficients for ethanol show a linear relation with the content but that for water exhibit a non-linear relation, which reveals the influence of ethanol on water structure in the mixture. Furthermore, the information of the water-ethanol clusters was found in the residual spectra after the fitting. Therefore, high order derivative can be an efficient way to improve the resolution of NIR spectra for understanding the interactions in aqueous solutions.<br /> (Copyright © 2019 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1873-3557
Volume :
213
Database :
MEDLINE
Journal :
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
Publication Type :
Academic Journal
Accession number :
30684883
Full Text :
https://doi.org/10.1016/j.saa.2019.01.059