Pan-heating of low-linolenic acid and partially hydrogenated soybean oils

被引:23
作者
Soheili, KC
Artz, WE
Tippayawat, P
机构
[1] Univ Illinois, Dept Food Sci & Human Nutr, Urbana, IL 61801 USA
[2] Dept Agr, Div Agr Chem, Bangkok, Thailand
关键词
genetically modified oil; low-linolenic acid soybean oil; pan heating;
D O I
10.1007/s11746-002-0475-9
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Genetically modified low-linolenic acid soybean oil (LL-SBO) was compared to partially hydrogenated soybean oil (PH-SBO). Samples were heated on a Teflon pan at similar to180degreesC until a selected end point of greater than or equal to20% polymer content was reached. High-performance size-exclusion chromatography analysis indicated the PH-SBO contained >20% polymer after 20 min of heating, whereas the LL-SBO sample contained >20% polymer after 10 min. Supercritical fluid chromatography analysis indicated degradation rates of 0.161 +/- 0.011 min(-1) for LL-SBO and 0.086 +/- 0.004 min(-1) for PH-SBO. The volatile compounds were identified and quantitated with static headspace-GC-MS. 1-Heptene (239.9 ppm) and hexanal (1486.1 ppm) were present at the greatest concentration among the volatile compounds in LL-SBO. The volatile compounds present in the greatest concentrations in heated PH-SBO were hexanal (376.9 ppm) and pentane (82.1 ppm). After 10 min of heating, the LL-SBO oil FFA value (2.66%), p-anisidine value (386.5 abs/g oil), Food Oil Sensor reading (18.75), and color intensity (Y = 4.0, R = 1.0) were significantly greater than those of PH-SBO after 14 min of heating (4.28%, 298.5 abs/g oil, 16.08, Y = 1.0, R = 0.1, respectively). There was a significant difference in the degradation rates between LL-SBO and PH-SBO (P < 0.05). The PH-SBO was more stable than the LL-SBO.
引用
收藏
页码:287 / 290
页数:4
相关论文
共 14 条
[1]  
*AM OIL CHEM SOC, 1990, OFF METH REC PRACT A, V1
[2]   Esterified propoxylated glycerol soyate, a fat substitute model compound, and soy oil after heating [J].
Artz, WE ;
Soheili, KC ;
Arjona, IM .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1999, 47 (09) :3816-3821
[3]  
Bennett B., 1997, Food Processing, USA, V58, P39
[4]  
Billek G., 1983, DIETARY FATS HLTH, P70
[5]  
DAGERSKOG M, 1978, LEBENSM WISS TECHNOL, V11, P306
[6]   ANALYSIS OF AUTO-OXIDIZED FATS BY GAS CHROMATOGRAPHY-MASS SPECTROMETRY .7. VOLATILE THERMAL-DECOMPOSITION PRODUCTS OF PURE HYDROPEROXIDES FROM AUTO-OXIDIZED AND PHOTOSENSITIZED OXIDIZED METHYL OLEATE, LINOLEATE AND LINOLENATE [J].
FRANKEL, EN ;
NEFF, WE ;
SELKE, E .
LIPIDS, 1981, 16 (05) :279-285
[7]  
Haumann B. Fitch, 1997, INFORM, V8, P804
[8]  
OHTA S, 1966, YUKAGAKU, V34, P33
[9]  
OUCHI GI, 1992, LC GC-MAG SEP SCI, V10, P524
[10]   THERMAL-DECOMPOSITION OF METHYL OLEATE HYDROPEROXIDES AND IDENTIFICATION OF VOLATILE COMPONENTS BY GAS CHROMATOGRAPHY-MASS SPECTROMETRY [J].
SELKE, E ;
FRANKEL, EN ;
NEFF, WE .
LIPIDS, 1978, 13 (07) :511-513