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101.
102.
103.
W. Dennis Pocklington 《Journal of the American Oil Chemists' Society》1992,69(8):789-793
The development, by collaborative study, of a standardized method for the determination of tetrachloroethylene in olive oils
is described. The results of the study, which was carried out in 1989 under the direction of the International Olive Oil Council
(IOOC), are presented and show that tetrachloroethylene can be readily determined, to an acceptable degree of precision, by
gas-liquid chromatography with electron capture detection. A limited number of results obtained for the determination of trichloroethylene
and chloroform by the same method indicate that a similar precision could be obtained with the method when determining these
solvents also. 相似文献
104.
Stuart M. Barlow Anthony P. Bimbo Eric L. Miller Snorri Thorisson D. E. Walters 《Journal of the American Oil Chemists' Society》1997,74(9):1077-1083
Twenty-two laboratories participated in a collaborative test to determine the iodine value (IV) of eight samples of fish oil
(four with IV<150, four with IV>150) with either carbon tetrachloride (AOCS Official Method Cd 1–25) or cyclohexane (AOCS
Recommended Practice Cd 1b-87) as solvent and either 1 or 2 h of reaction time. Laboratories received coded duplicate samples
(hidden duplicates) and carried out duplicate determinations on each oil by each solvent-time combination (open duplicates).
Replacing carbon tetrachloride with cyclohexane resulted in a lower IV (P<0.001). The decrease averaged 1.6 IV units for low-IV oils and 3.8 IV units for high-IV oils; this difference in response
of 2.2 IV units between low- and high-IV oils was significant (P<0.001). Increasing the reaction time had a relatively small effect (0.34±0.18). There was no interaction of reaction time
with solvent or oil type. Cyclohexane caused emulsions, which made it difficult to titrate residual iodine and thus increased
the variability of the determination. The repeatability standard deviations (s
r
), based on hidden duplicates, for 1-h reaction time with carbon tetrachloride and cyclohexane were 2.17 and 3.35, respectively.
The corresponding reproducibility standard deviations were 2.73 and 4.53. 相似文献
105.
106.
Alternative hydrocarbon solvents for cottonseed extraction 总被引:3,自引:0,他引:3
P. J. Wan D. R. Pakarinen R. J. Hron Sr. O. L. Richard E. J. Conkerton 《Journal of the American Oil Chemists' Society》1995,72(6):653-659
Hexane has been used for decades to extract edible oil from cottonseed. However, due to increased regulations affecting hexane
because of the 1990 Clean Air Act and potential health risks, the oil-extraction industry urgently needs alternative hydrocarbon
solvents to replace hexane. Five solvents,n-heptane, isohexane, neohexane, cyclohexane, and cylopentane, were compared with commercial hexane using a benchscale extractor.
The extractions were done with a solvent to cottonseed flake ratio of 5.5 to 1 (w/w) and a miscella recycle flow rate of 36
mL/min/sq cm (9 gal/min/sq ft) at a temperature of 10 to 45°C below the boiling point of the solvent. After a 10-min single-stage
extraction, commercial hexane removed 100% of the oil from the flakes at 55°C; heptane extracted 100% at 75°C and 95.9% at
55°C; isohexane extracted 93.1% at 45°C; while cyclopentane, cyclohexane, and neohexane removed 93.3, 89.4, and 89.6% at 35,
55, and 35°C, respectively. Each solvent removed gossypol from cottonseed flakes at a different rate, with cyclopentane being
most and neohexane least effective. Based on the bench-scale extraction results and the availability of these candidate solvents,
heptane and isohexane are the alternative hydrocarbon solvents most likely to replace hexane.
Presented in part at the AOCS Annual Meeting & Expo, Atlanta, Georgia, May 1994. 相似文献
107.
108.
土壤有效磷测试方法浅析 总被引:2,自引:0,他引:2
对有效磷的两种测定方法进行比较,讨论了两种方法之间的相关性及相关系数,为土壤有效磷的测定寻求更省时,省力的测试方法。 相似文献
109.
110.