孟庆顺,卜媛媛,王 悦,孙 丽,赵 燕,周义国,刘 蔷,陈长毅.气相色谱法测定白酒中醇类及酯类[J].食品安全质量检测学报,2021,12(11):4666-4671
气相色谱法测定白酒中醇类及酯类
Determination of alcohols and esters in liquor by gas chromatography
投稿时间:2021-02-26  修订日期:2021-06-10
DOI:
中文关键词:  气相色谱法  白酒  醇类  酯类  氢火焰离子化检测器  香型
英文关键词:gas chromatography  liquor  alcohol  esters  hydrogen flame ionization detector  scent
基金项目:
作者单位
孟庆顺 淮安市食品药品检验所 
卜媛媛 淮安市食品药品检验所 
王 悦 淮安市食品药品检验所 
孙 丽 淮安市食品药品检验所 
赵 燕 淮安市食品药品检验所 
周义国 淮安市食品药品检验所 
刘 蔷 淮安市食品药品检验所 
陈长毅 淮安市食品药品检验所 
AuthorInstitution
MENG Qing-Shun Huai’an Institute for Food and Drug Control 
BU Yuan-Yuan Huai’an Institute for Food and Drug Control 
WANG Yue Huai’an Institute for Food and Drug Control 
SUN Li Huai’an Institute for Food and Drug Control 
ZHAO Yan Huai’an Institute for Food and Drug Control 
ZHOU Yi-Guo Huai’an Institute for Food and Drug Control 
LIU Qiang Huai’an Institute for Food and Drug Control 
CHEN Chang-Yi Huai’an Institute for Food and Drug Control 
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中文摘要:
      目的 建立气相色谱法测定白酒中醇类和酯类的分析方法。方法 样品前期处理简单, 以叔戊醇为内标物, 进行内标法标准曲线定量, 采用FID氢火焰离子化检测器和毛细管色谱柱DB-FFAP (50 m× 0.32 mm, 0.50 μm)及程序升温进行测定, 检测器温度为300 ℃, 进样口温度230 ℃, 进样量0.5 μL。结果 各醇类及酯类混合标准溶液在相应的浓度范围内线性皆良好, 相关系数r均大于0.999, 检出限为3~9 mg/L (S/N=3), 定量限为10~30 mg/L (S/N=10), 回收率为88.25%~98.75%, 相对标准偏差(relative standard deviation, RSD)为2.75%~3.84% (n=6)。结论 该方法简化了操作步骤, 一次进样可以同时检测8种常规的醇类和酯类, 提高工作效率和仪器的利用率, 且回收率高, 重现性和精密度良好, 测定结果准确可靠, 满足白酒中醇类和酯类含量的定量分析。
英文摘要:
      Objective To establish a method for the determination of alcohols and esters in liquor by gas chromatography. Methods The sample was pretreated simply, 2-methyl-2-butanol was used as internal standard, the standard curve was quantified by internal standard method, and the sample was determined by flame ionization detector (FID), capillary column DB-FFAP (50 m×0.32 mm, 0.50 μm) and programmed temperature, the detector temperature was 300 ℃, the sample inlet temperature was 230 ℃, the sample volume was 0.5 μL. Results The standard solutions of alcohols and esters had good linearity in the corresponding concentration range, the correlation coefficients r were greater than 0.999, the detection limits were 3?9 mg/L (S/N=3) , the quantitative limits were 10-30 mg/L (S/N =10), the recovery rates were 88.25%?98.75% , relative standard deviations (RSDs) were 2.75%?3.84% (n=6). Conclusion The method simplified the operation steps, one injection can detect 8 kinds of alcohol and ester at the same time, improve the work efficiency and the utilization rate of the instrument, with high recovery, good reproducibility and precision, the determination results are accurate and reliable, meet the alcohols and esters content in liquor of quantitative analysis.
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