Effect of elevated temperature and UV radiation on molecular structure of linoleic acid by ATR-IR and two-dimensional correlation spectroscopy

The effect of elevated temperature (44 °C) and ultraviolet (UV) radiation on molecular structure of linoleic acid (LA) was studied by Attenuated Total Reflection Infrared (ATR-IR) spectroscopy. To obtain more detailed information on molecular mechanism of these changes we applied moving-window analy...

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Veröffentlicht in:Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy Molecular and biomolecular spectroscopy, 2020-09, Vol.238, p.118436, Article 118436
Hauptverfasser: Olsztyńska-Janus, S., Czarnecki, M.A.
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Sprache:eng
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Zusammenfassung:The effect of elevated temperature (44 °C) and ultraviolet (UV) radiation on molecular structure of linoleic acid (LA) was studied by Attenuated Total Reflection Infrared (ATR-IR) spectroscopy. To obtain more detailed information on molecular mechanism of these changes we applied moving-window analysis and two-dimensional correlation spectroscopy (2DCOS). Analysis of the time-dependent ATR-IR spectra of LA before and after UV irradiation revealed the structural changes in molecules of LA. The extent of these changes was significantly higher after an application of UV radiation. During 24 h experiment temperature was constant, therefore the spectral changes result from relatively slow processes (and requiring more energy), e.g. cis/trans isomerization, disruption of the C=C double bonds and partial breaking of hydrogen bonds in the cyclic dimers. As a side effect of these structural changes one can observe variations in the orientation of the chains. It is of note that the methyl and methylene groups reveal slightly different behaviour. [Display omitted] •Effects of elevated temperature and UV radiation on LA were studied by ATR-IR and 2D-COS spectroscopy.•Time-dependent ATR-IR spectra revealed the structural modifications of LA.•The extent of spectral changes increases after sample irradiation.•The primary process observed in LA was cis-trans isomerization.•The secondary changes result from disruption of the C=C bonds and partial breaking of HB in the cyclic dimers of LA.
ISSN:1386-1425
1873-3557
DOI:10.1016/j.saa.2020.118436