食用植物油中4种氯丙醇脂肪酸酯的GC-MS测定方法研究  被引量:9

Determination of four kinds of chloropropanols fatty acid esters in edible vegetable oil by GC-MS

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作  者:柏文良[1] 杜业刚[1] 陈萌[1] 张浩英[1] 李碧芳[1] 

机构地区:[1]深圳市计量质量检测研究院,广东深圳518109

出  处:《中国油脂》2017年第2期81-84,112,共5页China Oils and Fats

摘  要:采用气相色谱-质谱(GC-MS)联用技术,建立了同时测定食用植物油中3-氯-1,2-丙二醇脂肪酸酯(3-MCPD酯)、2-氯-1,3-丙二醇脂肪酸酯(2-MCPD酯)、1,3-二氯-2-丙二醇脂肪酸酯(1,3-DCP酯)和2,3-二氯-1-丙二醇脂肪酸酯(2,3-DCP酯)含量的分析方法。该方法在0.005~0.5 mg/L范围内线性关系良好,检出限0.1 mg/kg,定量限0.2 mg/kg,加标回收率在97.2%~106.0%之间,相对标准偏差在3.4%~7.1%之间。该方法操作简便,灵敏度高,重复性好,定性定量准确,对仪器污染小,能满足食用植物油中氯丙醇酯的检测需求。A method for the simultaneous determination of the contents of 3 - monochloropropane - 1,2 - diol (3 - MCPD ester), 2 - monochloropropane - 1,3 - diol (2 - MCPD ester), 1,3 - dichloropropane - 2 - ol ( 1, 3 - DCP ester) and 2,3 - dichloropropane - 1 - o1(2,3 - DCP ester) in edible vegetable oil was es- tablished by gas chromatography - mass spectrography ( GC - MS). The method showed good linear rela- tionship in the range of 0.005 - 0.5 mg/L. The detection limit and quantification limit were 0.1 mg/kg and 0.2 mg/kg respectively. The recovery rate was between 97.2% - 106.0% , and the relative stand- ard deviation was between 3.4% - 7.1%. The method was easily operated with good sensitivity, good repeatability, precise quanlification and quantification and little pollution to instrument, and it could meet the determination demand of chloropropanols fatty acid esters in edible vegetable oil.

关 键 词:食用植物油 3-MCPD酯 2-MCPD酯 1 3-DCP酯 2 3-DCP酯 GC-MS 

分 类 号:TS225.1[轻工技术与工程—粮食、油脂及植物蛋白工程] TS201.6[轻工技术与工程—食品科学与工程]

 

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