Raman spectroscopic detection of polyene-length distribution for high-sensitivity monitoring of photo- and thermal degradation of polyvinylchloride

• Published in: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy Vol. 252; p. 119494
• Main Authors: Kuznetsov, Sergey M., Sagitova, Elena A., Prokhorov, Kirill A., Nikolaeva, Gulnara Yu, Mendeleev, Dmitry I., Donfack, Patrice, Materny, Arnulf
• Format: Journal Article
• Language: English
• Published: England Elsevier B.V 05.05.2021
• Subjects: Chain length; Polyene; Polyvinylchloride degradation; Resonance Raman spectroscopy; Polyvinylchloride degradation; Polyene; Chain length; Resonance Raman spectroscopy
• ISSN: 1386-1425; 1873-3557
• DOI: 10.1016/j.saa.2021.119494

[Display omitted] •Photo- and thermally degraded PVC contains polyenes of various lengths and amounts.•Resonance Raman at 488, 514, 532, and 647 nm detects polyenes with 10–25C=C bonds.•Novel 647 nm resonance excitation yields enhanced Raman signatures of long polyenes.•C=C band deconvolution reveals asymmetric polyene length distribution.•C−C band position in degraded PVC Raman spectra is a measure of polyene length. The degradation of the ubiquitous polyvinylchloride (PVC) material under the influence of various factors is known to result commonly in polyene formation. Such polyene defects occur in the form of conjugated aliphatic chains with different lengths and contents, and their sensitive and length-specific monitoring is important for the assessment of PVC degradation. Here, we report on the resonance-enhanced Raman signatures of polyene sequences of varying lengths in photo- and thermally degraded PVC films. The lengths of polyene segments have been estimated based on their selectively enhanced and spectrally resolved contributions to the Raman bands assigned to the stretching vibrations of conjugated double carbon bonds. Using deconvolution analysis of a characteristic Raman band of polyenes, we especially demonstrate that the spectral signatures of polyene segments corresponding to other various electronic resonances contribute to the Raman spectral envelope observed at a given resonant excitation. In most cases, we observe an asymmetric band profile, indicating an asymmetric length distribution of polyene defects formed in PVC films upon a mild degradation extent less than 1% mass loss. We also demonstrate that the wavenumber (ν1) of the stretching vibrations of single carbon bonds in the polyene sequences of degraded PVC is inversely related to the number (n) of double carbon bonds by an empirical equation n=476·cm-1/ν1-1082·cm-1. To the best of our knowledge, while considering different laser excitations spanning the range of possible electronic resonances from blue to near-infrared for Raman investigations, the present work includes (i) the first Raman spectral deconvolution study for the 532.0 nm excitation wavelength used in most portable Raman probes nowadays and (ii) the screening of polyene defects also beyond the red edge of the visible spectrum and the evidence of a resonance-enhanced polyene signal at 647.1 nm. Important new information has been obtained about polyene lengths and spectral distribution for PVC, whose critical physical properties ranging from flexibility to electrical resistance are severely affected by polyene formation.