High-resolution proton nuclear magnetic resonance (H-1-NMR) spectroscopv (400-600 MHz) was applied to the quantitative analysis of hydroperoxide decomposition products in thermally oxidized oils, Different oils (olive, sunflower and soybean) were heated in a thermostatic bath (180 degrees C for 360 min). Proton NMR quantitative aldehyde analysis (n-alkanals, trans-2-alkenals, 4-hydroxy-trans-2-alkenals, alka-2,4-dienals) of fifteen oil samples (0, 60, 120, 240 and 360 minute heating) was compared with that of total polar compounds through silica column chromatography and of short-chain fatty acids. A good linear relationship (R-2 = 0.94) was found between the unsaturated aldehyde level and the amount of methyl-octanoate as well as between total aldehyde determined by H-1-NMR and total polar compounds (R-2 = 0.92). The same NMR sensitivity obtained at 400 MHz through 3000 scans was reached with only 64 scans for a total acquisition time of 2 min at 600 MHz. The potential use of H-1-NMR as a direct tool to monitor the quality and oxidative degradation in heated and fried oils is discussed.
Quantitative evaluation of the aldehydes formed in heated vegetable oils using high resolution proton-NMR spectroscopy / Sacchi, Raffaele; Falcigno, Lucia; Paduano, Antonello; Ambrosino, MARIA LUISA; Savarese, Maria; DE GIULIO, B.; Addeo, Francesco; Paolillo, Livio. - In: LA RIVISTA ITALIANA DELLE SOSTANZE GRASSE. - ISSN 0035-6808. - 6:(2006), pp. 257-263.
Quantitative evaluation of the aldehydes formed in heated vegetable oils using high resolution proton-NMR spectroscopy
SACCHI, RAFFAELE;FALCIGNO, LUCIA;PADUANO, ANTONELLO;AMBROSINO, MARIA LUISA;SAVARESE, MARIA;ADDEO, FRANCESCO;PAOLILLO, LIVIO
2006
Abstract
High-resolution proton nuclear magnetic resonance (H-1-NMR) spectroscopv (400-600 MHz) was applied to the quantitative analysis of hydroperoxide decomposition products in thermally oxidized oils, Different oils (olive, sunflower and soybean) were heated in a thermostatic bath (180 degrees C for 360 min). Proton NMR quantitative aldehyde analysis (n-alkanals, trans-2-alkenals, 4-hydroxy-trans-2-alkenals, alka-2,4-dienals) of fifteen oil samples (0, 60, 120, 240 and 360 minute heating) was compared with that of total polar compounds through silica column chromatography and of short-chain fatty acids. A good linear relationship (R-2 = 0.94) was found between the unsaturated aldehyde level and the amount of methyl-octanoate as well as between total aldehyde determined by H-1-NMR and total polar compounds (R-2 = 0.92). The same NMR sensitivity obtained at 400 MHz through 3000 scans was reached with only 64 scans for a total acquisition time of 2 min at 600 MHz. The potential use of H-1-NMR as a direct tool to monitor the quality and oxidative degradation in heated and fried oils is discussed.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.