• EI
  • Scopus
  • 中国科技期刊卓越行动计划项目资助期刊
  • 北大核心期刊
  • DOAJ
  • EBSCO
  • 中国核心学术期刊RCCSE A+
  • 中国精品科技期刊
  • JST China
  • FSTA
  • 中国农林核心期刊
  • 中国科技核心期刊CSTPCD
  • CA
  • WJCI
  • 食品科学与工程领域高质量科技期刊分级目录第一方阵T1
中国精品科技期刊2020
王晓曦, 王彦, 李静, 茹鑫, 闫超. 加压毛细管电色谱法同时测定植物油中4种抗氧化剂[J]. 华体会体育, 2015, (09): 273-277. DOI: 10.13386/j.issn1002-0306.2015.09.051
引用本文: 王晓曦, 王彦, 李静, 茹鑫, 闫超. 加压毛细管电色谱法同时测定植物油中4种抗氧化剂[J]. 华体会体育, 2015, (09): 273-277. DOI: 10.13386/j.issn1002-0306.2015.09.051
WANG Xiao-xi, WANG Yan, LI Jing, RU Xin, YAN Chao. Determination of four antioxidants in vegetable oils by pressurized capillary electrochromatography[J]. Science and Technology of Food Industry, 2015, (09): 273-277. DOI: 10.13386/j.issn1002-0306.2015.09.051
Citation: WANG Xiao-xi, WANG Yan, LI Jing, RU Xin, YAN Chao. Determination of four antioxidants in vegetable oils by pressurized capillary electrochromatography[J]. Science and Technology of Food Industry, 2015, (09): 273-277. DOI: 10.13386/j.issn1002-0306.2015.09.051

加压毛细管电色谱法同时测定植物油中4种抗氧化剂

Determination of four antioxidants in vegetable oils by pressurized capillary electrochromatography

  • 摘要: 采用加压毛细管电色谱-紫外检测,建立了一种适用于植物油中常见抗氧化剂的分离检测方法。使用1.8μm粒径的C18毛细管色谱柱,以乙腈-水(0.05%甲酸)为流动相进行梯度洗脱,泵流速为0.05m L/min,分流比为1∶200,分离电压为15k V,没食子酸丙酯(PG)、叔丁基对苯二酚(TBHQ)、丁基羟基茴香醚(BHA)、2,6-二叔丁基对甲酚(BHT)四种抗氧化剂可在8min内实现快速分离。各组分的检出限(S/N=3)分别为0.6、2.0、3.0、5.5μg/m L,线性关系良好,样品加标回收率在93.5%108.0%之间,RSD在0.3%1.3%之间。将所建立方法应用于植物油样品的分析,取得了良好的分析结果。 

     

    Abstract: A method for antioxidants analysis in vegetable oils was developed by using pressurized capillary electrochromatography( p CEC) with UV / Vis detection. The separations were performed on a C18 capillary column packed with 1.8μm particles. The mobile phase was acetonitrile / water containing 0.05% formic acid( p H3.2) at a pump flow rate of 0.05 m L / min with splitting ratio of 1 ∶ 200 and the separation voltage was 15 k V. Four antioxidants( PG,TBHQ,BHA,BHT) were baseline separated within 8min in gradient elution mode.The detection limits of each antioxidant( S / N = 3) were 0.6,2.0,3.0,5.5μg / m L respectively with good linear correlation.The method was applied to detect the regetable oils and the results was accurate. The spiked recoveries of vegetable oils were 93.5% ~108.0%,with RSD ranged 0.3% ~1.3%.

     

/

返回文章
返回