Tagging the oligomer-to-polymer crossover on EG and PEGs by infrared and Raman spectroscopies and by wavelet cross-correlation spectral analysis

被引:40
作者
Caccamo, M. T. [1 ]
Magazu, S. [1 ]
机构
[1] Univ Messina, Dipartimento Sci Matemat & Informat Sci Fis & Sci, Viale FS DAlcontres 31, I-98166 Messina, Italy
关键词
Ethylene glycol; PolyEthylene glycols; Infrared spectroscopy; Raman scattering; Wavelet analysis; Wavelet cross-Correlation; INCOHERENT NEUTRON-SCATTERING; POLYETHYLENE OXIDE; POLY(ETHYLENE OXIDE); AQUEOUS-SOLUTIONS; THERMAL-ANALYSIS; WATER-STRUCTURE; GENERAL-METHOD; DYNAMIC LIGHT; LIQUID-STATE; IN-VITRO;
D O I
10.1016/j.vibspec.2016.04.017
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Infrared and Raman spectra on pure ethylene glycol (EG) and on low molecular weight polyethylene glycols (PEGS) with increasing chain length have been collected and analysed in a wide spectral range in order to determine the oligomer-to-polymer regime crossover. Previous spectroscopic crossover determinations reported in literature dealt only with Raman investigation of the Disordered Longitudinal Acoustic Mode (D-LAM). The IR and Raman contribution features, when analysed in different spectral ranges, show a dramatic change as a function of the polymer chain length, signaling an oligomer-polymer crossover for a polymerization degree of m = 13. An innovative Wavelet Transform (WT) approach allows to confirm the above reported physical picture. In particular WT, differently from standard Principal Component Analysis (PCA) allows a multiscale analysis which permits to quantify the spectral shape modifications of different spectral regions of the collected IR and Raman spectra. It is shown that the wavelet cross-correlation parameters evaluated between each couple of the registered data, from EG to PEG 1000, change as a function of the polymer chain length, confirming that a plateau value is reached for m=13. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:222 / 227
页数:6
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