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中国精品科技期刊2020
王荣芳, 杨晓博, 陈剑桥, 李喜悦, 崔同. 顶空固相微萃取-气相色谱法测定山楂果胶酯化度[J]. 食品工业科技, 2016, (16): 56-60. DOI: 10.13386/j.issn1002-0306.2016.16.002
引用本文: 王荣芳, 杨晓博, 陈剑桥, 李喜悦, 崔同. 顶空固相微萃取-气相色谱法测定山楂果胶酯化度[J]. 食品工业科技, 2016, (16): 56-60. DOI: 10.13386/j.issn1002-0306.2016.16.002
WANG Rong-fang, YANG Xiao-bo, CHEN Jian-qiao, LI Xi-yue, CUI Tong. Determination of the esterification degree of hawthorn pectin by headspace solid-phase microexrtaction and gas chromatography[J]. Science and Technology of Food Industry, 2016, (16): 56-60. DOI: 10.13386/j.issn1002-0306.2016.16.002
Citation: WANG Rong-fang, YANG Xiao-bo, CHEN Jian-qiao, LI Xi-yue, CUI Tong. Determination of the esterification degree of hawthorn pectin by headspace solid-phase microexrtaction and gas chromatography[J]. Science and Technology of Food Industry, 2016, (16): 56-60. DOI: 10.13386/j.issn1002-0306.2016.16.002

顶空固相微萃取-气相色谱法测定山楂果胶酯化度

Determination of the esterification degree of hawthorn pectin by headspace solid-phase microexrtaction and gas chromatography

  • 摘要: 利用顶空固相微萃取与气相色谱联用(HS-SPME-GC)的方法测定山楂果胶的酯化度(包括甲酯化和乙酯化),对影响检测结果的萃取头种类、萃取温度、平衡时间、萃取时间、盐离子浓度、解吸温度、解吸时间进行了优化。结果表明,HS-SPME-GC测定山楂果胶酯化度较优条件为:5 m L山楂果胶溶液中加48.8%硫酸钠,在40℃下平衡20 min,用75μm CAR-PDMS萃取头在40℃下萃取30 min,然后在280℃的GC进样口解析60 s。该方法线性良好r≥0.9983,检出限1015 mg/L,加标回收率为95.6%116.2%。该方法快速、简便、准确。 

     

    Abstract: Headspace solid- phase microextraction and gas chromatography( HS- SPME- GC) were used for the qualitative determination of the esterification degree( methyl esterification and ethyl esterification) of haw pectin samples.HS- SPME experimental conditions,such as the type of fibers,extraction temperature,balance time,extraction time,salt concentrations,desorption temperature,desorption time were optimized.The best HS- SPMEGC performance was achieved under the following conditions: 5 m L pectin solution in headspace glass vial with addition of 48.8% Na2SO4,20 min balance time and 30 min extraction time at 40 ℃ using 75 μm CAR-PDMS fiber and 60 s desorption time in the GC inlet at 280 ℃.The correlation coefficient r was greater than 0.9983,the detection limits of the method were 10~15 mg / L,the recovery rates were 95.6% ~116.2%.The proposed method is simple,fast and accurate with high reproducibility.

     

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