scholarly journals Rapid Identification of Adulteration in Edible Vegetable Oils Based on Low-Field Nuclear Magnetic Resonance Relaxation Fingerprints

Foods ◽  
2021 ◽  
Vol 10 (12) ◽  
pp. 3068
Author(s):  
Zhi-Ming Huang ◽  
Jia-Xiang Xin ◽  
Shan-Shan Sun ◽  
Yi Li ◽  
Da-Xiu Wei ◽  
...  

Most current approaches applied for the essential identification of adulteration in edible vegetable oils are of limited practical benefit because they require long analysis times, professional training, and costly instrumentation. The present work addresses this issue by developing a novel simple, accurate, and rapid identification approach based on the magnetic resonance relaxation fingerprints obtained from low-field nuclear magnetic resonance spectroscopy measurements of edible vegetable oils. The relaxation fingerprints obtained for six types of edible vegetable oil, including flaxseed oil, olive oil, soybean oil, corn oil, peanut oil, and sunflower oil, are demonstrated to have sufficiently unique characteristics to enable the identification of the individual types of oil in a sample. By using principal component analysis, three characteristic regions in the fingerprints were screened out to create a novel three-dimensional characteristic coordination system for oil discrimination and adulteration identification. Univariate analysis and partial least squares regression were used to successfully quantify the oil adulteration in adulterated binary oil samples, indicating the great potential of the present approach on both identification and quantification of edible oil adulteration.

1988 ◽  
Vol 66 (10) ◽  
pp. 2570-2574 ◽  
Author(s):  
Alan S. Tracey ◽  
Michael J. Gresser

A variety of alkyl vanadates has been studied by 51V nuclear magnetic resonance spectroscopy. It was found that the equilibrium constant for condensation of vanadate with alcohols is insensitive to whether the hydroxyl group is primary, secondary, or tertiary. These products, however, have characteristic vanadium chemical shifts that allow assignment of nmr signals to the appropriate ester. It was also found that chemical shifts are additive in the sense that the chemical shifts of the esters ROVO3H− are one half the chemical shift of the diesters (RO)2VO2− when those shifts are given relative to −559 ppm. This effect is independent of whether the signals are to high or low field of −559 ppm and the additivity extends to mixed ligand systems. This value of −559 ppm is close but not equal to the chemical shift of the vanadate monoanion, H2VO41−, which is at −561 ppm. These results are at variance with arguments concerning the effects of ligand bulkiness on chemical shifts of vanadium(V) complexes.


Measurement ◽  
2019 ◽  
Vol 137 ◽  
pp. 673-682 ◽  
Author(s):  
E. Förster ◽  
C.C. Fraenza ◽  
J. Küstner ◽  
E. Anoardo ◽  
H. Nirschl ◽  
...  

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