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Separation of oryzanol from crude rice bran oil.

机译:从粗米糠油中分离谷维素。

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The separation of oryzanol from crude rice bran oil was investigated with the ultimate goal of industrial application. The oryzanol was concentrated from the crude oil and then isolated by silica gel column chromatography. Preparation of the oryzanol concentrate was attempted by the extraction of unsaponifiable matter, solvent extraction and step-wise elution chromatography. Methanol, ethanol and dimethylformamide were each evaluated for the solvent extraction. The column chromatographic separation was optimized with respect to mobile phase, flowrate, column height, and column width.; The dimethylformamide extraction of the crude oil proved to be the optimal method of oryzanol concentration with respect to oryzanol recovery and concentration in the extract. This method produced a fraction containing 8.4 {dollar}pm{dollar} 0.6% oryzanol, concentrating oryzanol by a factor of 9.7 {dollar}pm{dollar} 0.6 from the crude oil. The column chromatographic system, with the mobile phase toluene/ethyl acetate 90:10 by volume, separated oryzanol from the less polar compounds in the extracted concentrate. However, oryzanol could not be isolated from the more polar components. Variations in flowrate, column height, and column width did not significantly enhance the separation.; Scale-up of the dimethylformamide extraction did not affect oryzanol recovery. Furthermore, extractions with fresh and recycled solvent showed no difference in the extracted oryzanol concentrate. Therefore, pilot-plant scale-up of this extraction should be considered. Isolation of oryzanol from the concentrate by column chromatography should be further investigated with the use of reverse-phase silica as the adsorbent.
机译:以工业应用为最终目标,研究了从米糠油中分离谷维素的方法。从原油中浓缩谷维素,然后通过硅胶柱色谱法分离。尝试通过不皂化物的提取,溶剂提取和逐步洗脱色谱法来制备谷维素浓缩物。分别评估甲醇,乙醇和二甲基甲酰胺的溶剂萃取。对色谱柱的分离进行了流动相,流速,柱高和柱宽的优化。相对于提取物中的谷维素回收率和浓度,原油的二甲基甲酰胺提取被证明是谷维素浓缩的最佳方法。该方法产生了含有8.4 {pm} pm {dollar} 0.6%的谷维素的馏分,从原油中将谷维素醇浓缩了9.7 {dollar} pm {dollar} 0.6。流动相甲苯/乙酸乙酯的体积比为90:10的柱色谱系统将谷维素与提取液中极性较小的化合物分离。但是,谷维素不能从极性较大的组分中分离出来。流速,色谱柱高度和色谱柱宽度的变化并没有显着增强分离效果。放大二甲基甲酰胺提取液不会影响谷维素的回收率。此外,用新鲜和循环溶剂萃取在提取的谷维素浓缩物中没有差异。因此,应考虑将该提取物扩大到中试规模。应通过使用反相硅胶作为吸附剂,进一步研究通过柱色谱法从浓缩物中分离出谷维素的方法。

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