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Food Lipids: Chemistry, Nutrition, and Biotechnology

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Figure 1 The mid-infrared spectrum of an edible oil collected on an attenuated total reflectance<br />

crystal. Labels indicate absorption b<strong>and</strong>s or regions associated with triacylglycerols<br />

or other constituents that may be present in an oil or free fatty acid. (From Ref. 137.)<br />

region where compounds containing hydroxyl groups are absorbed, including water<br />

(H-OH) <strong>and</strong> hydroperoxides (RO-H) <strong>and</strong> their breakdown products. At some lower<br />

frequencies (3025–2850 cm �1 ) is the CH stretching region where three b<strong>and</strong>s are<br />

visible: a weak cis double bond CH absorption (CH—CH) <strong>and</strong> strong bonds due to<br />

the CH 2 groups of the aliphatic chains of TAGs as well as the terminal methyl groups.<br />

Just beyond this region is secondary oxidation products of lipids such as aldehydes<br />

<strong>and</strong> ketones that absorb energy albeit weakly. Toward the center of the spectrum is<br />

a very strong b<strong>and</strong> due to the C—O stretching absorption due to the ester linkage<br />

attaching the fatty acids to the glycerol backbone of TAGs. Next to it is a b<strong>and</strong> due<br />

to COOH group of FFAs if the lipid is hydrolyzed. In the same region there would<br />

be carbonyl absorption b<strong>and</strong>s of aldehydes (R-CHO) <strong>and</strong> ketones (R-CO-R) if the<br />

oil is oxidized. Continuing to lower frequencies area is the finger printing region<br />

(1500–900 cm �1 ) as the pattern of b<strong>and</strong>s in this region is very characteristic of<br />

molecular composition of the lipid <strong>and</strong> could be used to identify different components.<br />

At the low-frequency end of the fingerprinting region, a b<strong>and</strong> due to the<br />

CH—CH bonding absorption of isolated trans double bonds could be seen when<br />

trans-containing TAGs are present in the oil. The corresponding absorption of conjugated<br />

dienes containing trans-trans <strong>and</strong> cis-trans double bonds appears at slightly<br />

hi h f i i idi d l d f id i i il B d<br />

Copyright 2002 by Marcel Dekker, Inc. All Rights Reserved.

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