中国油脂
中國油脂
중국유지
CHINA OILS AND FATS
2015年
4期
69-73
,共5页
黄贤校%邹彦平%高媛媛%杨苗
黃賢校%鄒彥平%高媛媛%楊苗
황현교%추언평%고원원%양묘
乳木果液油%甲酯化%转酯化%分子蒸馏%三萜醇%甾醇
乳木果液油%甲酯化%轉酯化%分子蒸餾%三萜醇%甾醇
유목과액유%갑지화%전지화%분자증류%삼첩순%치순
shea olein%methyl esterification%transesterification%molecular distillation%triterpene%sterol
以乳木果液油为原料,经甲酯化后得到低酸值的乳木果液油,通过转酯化把甘三酯转化为脂肪酸甲酯,通过分子蒸馏把脂肪酸甲酯和生物活性物质分为轻组分和重组分,重组分(生物活性物质)再经过溶剂结晶进一步提高生物活性物质含量。通过单因素实验确定较好的甲酯化工艺条件为:反应温度70℃,反应时间3 h,醇油质量比3∶10,浓硫酸添加量3%;在此条件下,乳木果液油的酸值(KOH)从56.1 mg/g降至2.1 mg/g,游离脂肪酸转化率达到96.3%。通过单因素实验确定的较佳分子蒸馏条件为:进料速率2 mL/min,刮膜转速250 r/min,蒸馏温度150℃,真空度0.1 Pa;在此条件下蒸馏,生物活性物质在重组分中的回收率达95.9%,生物活性物质含量可达68.8%。乳木果液油经过甲酯化、转酯化、分子蒸馏和结晶得到的产品中三萜醇和甾醇总含量可达69.80%,生物活性物质含量可达83.18%。
以乳木果液油為原料,經甲酯化後得到低痠值的乳木果液油,通過轉酯化把甘三酯轉化為脂肪痠甲酯,通過分子蒸餾把脂肪痠甲酯和生物活性物質分為輕組分和重組分,重組分(生物活性物質)再經過溶劑結晶進一步提高生物活性物質含量。通過單因素實驗確定較好的甲酯化工藝條件為:反應溫度70℃,反應時間3 h,醇油質量比3∶10,濃硫痠添加量3%;在此條件下,乳木果液油的痠值(KOH)從56.1 mg/g降至2.1 mg/g,遊離脂肪痠轉化率達到96.3%。通過單因素實驗確定的較佳分子蒸餾條件為:進料速率2 mL/min,颳膜轉速250 r/min,蒸餾溫度150℃,真空度0.1 Pa;在此條件下蒸餾,生物活性物質在重組分中的迴收率達95.9%,生物活性物質含量可達68.8%。乳木果液油經過甲酯化、轉酯化、分子蒸餾和結晶得到的產品中三萜醇和甾醇總含量可達69.80%,生物活性物質含量可達83.18%。
이유목과액유위원료,경갑지화후득도저산치적유목과액유,통과전지화파감삼지전화위지방산갑지,통과분자증류파지방산갑지화생물활성물질분위경조분화중조분,중조분(생물활성물질)재경과용제결정진일보제고생물활성물질함량。통과단인소실험학정교호적갑지화공예조건위:반응온도70℃,반응시간3 h,순유질량비3∶10,농류산첨가량3%;재차조건하,유목과액유적산치(KOH)종56.1 mg/g강지2.1 mg/g,유리지방산전화솔체도96.3%。통과단인소실험학정적교가분자증류조건위:진료속솔2 mL/min,괄막전속250 r/min,증류온도150℃,진공도0.1 Pa;재차조건하증류,생물활성물질재중조분중적회수솔체95.9%,생물활성물질함량가체68.8%。유목과액유경과갑지화、전지화、분자증류화결정득도적산품중삼첩순화치순총함량가체69.80%,생물활성물질함량가체83.18%。
With shea olein as raw material, low acid value shea olein was obtained by methyl esterification, then triglyceride was transformed into fatty acid methyl ester by transesterification. After the fatty acid methyl ester and bioactive compounds were separated into light fraction and heavy fraction by molecular dis-tillation, the heavy fraction ( bioactive compounds) was crystallized with solvent to further improve the con-tent of active compounds. The optimal methyl esterification conditions were determined by single factor ex-periment as follows:reaction temperature 70℃, reaction time 3 h, mass ratio of methanol to oil 3∶10, dos-age of concentrated sulfuric acid 3%. Under these conditions, acid value of shea olein reduced from 56. 1 mgKOH/g to 2. 1 mgKOH/g, and the conversion rate of free fatty acids reached 96. 3%. The optimal con-ditions of molecular distillation were obtained by single factor experiment as follows:feed rate 2 mL/min, scraper speed 250 r/min, distillation temperature 150℃, vacuum degree 0. 1 Pa. Under these conditions, the recovery of the bioactive compounds in heavy fraction was 95. 9% and the content of bioactive com-pounds was up to 68. 8%. By the methods of methyl esterification, transesterification, molecular distillation and crystallization, the total content of triterpene and sterol in the product could reach 69. 80%, and the content of bioactive compounds could achieve 83. 18%.