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顶空-气相色谱法测定食用植物油中溶剂残留的方法研究
引用本文:章晴,陈士恒,高丁,史晓梅,杨永坛.顶空-气相色谱法测定食用植物油中溶剂残留的方法研究[J].分析测试技术与仪器,2015(4):225-230.
作者姓名:章晴  陈士恒  高丁  史晓梅  杨永坛
作者单位:中粮营养健康研究院, 北京市营养健康与食品安全重点实验室, 北京 102209;中粮营养健康研究院, 北京市营养健康与食品安全重点实验室, 北京 102209;中粮营养健康研究院, 北京市营养健康与食品安全重点实验室, 北京 102209;中粮营养健康研究院, 北京市营养健康与食品安全重点实验室, 北京 102209;中粮营养健康研究院, 北京市营养健康与食品安全重点实验室, 北京 102209
摘    要:建立顶空-气相色谱法测定食用植物油中六号溶剂残留量的分析方法.通过优化顶空进样器的平衡温度和平衡时间,使六号溶剂的主要组分完全分离,采用外标法进行定量.在2.0~100.0 mg/kg质量分数范围内,线性关系良好.在低、中、高3个加标水平下,平均回收率是98.2%~99.2%,相对标准偏差是小于2%.方法简便、准确,适合于食用植物油中六号溶剂残留量的测定.

关 键 词:顶空-气相色谱法  溶剂残留  食用植物油
收稿时间:2015/10/19 0:00:00
修稿时间:2015/11/12 0:00:00

Study on Determination of Residual Solvent in Edible Vegetable Oils by Headspace-Gas Chromatography
ZHANG Qing,CHEN Shi-heng,GAO Ding,SHI Xiao-mei and YANG Yong-tan.Study on Determination of Residual Solvent in Edible Vegetable Oils by Headspace-Gas Chromatography[J].Analysis and Testing Technology and Instruments,2015(4):225-230.
Authors:ZHANG Qing  CHEN Shi-heng  GAO Ding  SHI Xiao-mei and YANG Yong-tan
Institution:COFCO Nutrition & Health Research Institute, Beijing Key Laboratory of Nutrition Health and Food Safety, Beijing 102209, China;COFCO Nutrition & Health Research Institute, Beijing Key Laboratory of Nutrition Health and Food Safety, Beijing 102209, China;COFCO Nutrition & Health Research Institute, Beijing Key Laboratory of Nutrition Health and Food Safety, Beijing 102209, China;COFCO Nutrition & Health Research Institute, Beijing Key Laboratory of Nutrition Health and Food Safety, Beijing 102209, China;COFCO Nutrition & Health Research Institute, Beijing Key Laboratory of Nutrition Health and Food Safety, Beijing 102209, China
Abstract:A method to determine the residual solvent in edible vegetable oils using headspace-gas chromatography is established. The main components of solvent No.6 were separated completely under the optimized equilibrium temperature and equilibrium time conditions of the headspace auto-sampler.The amount was quantified by an external standard method. The linear relationship was satisfied from 2.0 to 100.0 mg/kg. The average spiked recoveries at three levels were in the range of 98.2%~99.2% and the relative standard deviations(n=6) were less than 2%.With features such as simpleness and accuracy, this method is suitable for the determination of residual solvent in edible vegetable oils.
Keywords:headspace-gas chromatography  residual solvent  edible vegetable oil
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