食品科学 ›› 2021, Vol. 42 ›› Issue (18): 292-297.doi: 10.7506/spkx1002-6630-20200911-143

• 安全检测 • 上一篇    下一篇

基于酸度控制的吸收光谱法测定饮料中共存的柠檬黄和日落黄

江虹,庞向东,蒋翠,冉红杰,付玲,刘璐   

  1. (长江师范学院化学化工学院,重庆 408100)
  • 发布日期:2021-09-29
  • 基金资助:
    重庆市教委科技基金项目(S201910647003);长江师范学院科技基金项目(2018CXX111)

Determination of Tartrazine and Sunset Yellow in Drinks by Absorption Spectrometry Based on Acidity Control

JIANG Hong, PANG Xiangdong, JIANG Cui, RAN Hongjie, FU Ling, LIU Lu   

  1. (College of Chemistry and Chemical Engineering, Yangtze Normal University, Chongqing 408100, China)
  • Published:2021-09-29

摘要: 建立快速、准确测定饮料中共存着色剂柠檬黄与日落黄的吸收光谱检测方法。在一定酸度的Tris-HCl介质中,乙基紫与柠檬黄(pH 5.69)和日落黄(pH 8.68)反应生成离子缔合物,在波长506 nm处产生能定量分析共存色素中柠檬黄的特征吸收峰,在波长646 nm处产生能定量分析共存色素中日落黄的特征吸收峰,它们的表观摩尔吸光系数分别为1.37×105 L/(mol·cm)(柠檬黄体系)和7.68×104 L/(mol·cm)(日落黄体系)。柠檬黄在0.04~9.6 mg/L范围内与吸光度绝对值呈线性关系,检出限为0.024 mg/L,定量限为1.29 mg/kg;日落黄在0.04~6.3 mg/L范围内与吸光度呈线性关系,检出限为0.031 mg/L,定量限为1.68 mg/kg。该法用于实际样品分析,加标回收率为97.0%~104%(柠檬黄体系)和97.3%~103%(日落黄体系),相对标准偏差(n=5)为1.5%~2.6%(柠檬黄体系)和1.2%~2.6%(日落黄体系)。该法简便、快速,用于饮料中共存柠檬黄和日落黄的测定,结果满意。

关键词: 乙基紫;柠檬黄;日落黄;吸收光谱法;酸度控制

Abstract: A novel absorption spectrometric method for the rapid and accurate determination of the colorants tartrazine and sunset yellow in beverages was established. In Tris-HCl medium with a certain acidity, ethyl violet could react with tartrazine (pH 5.69) and sunset yellow (pH 8.68) to form an ion association complex. At 506 and 646 nm, tartrazine and sunset yellow exhibited characteristic absorption, respectively, allowing their quantitative analysis. Their apparent molar absorption coefficients were 1.37 × 105 and 7.68 × 104 L/(mol·cm), respectively. There was a linear relationship between the concentration of tartrazine in the range of 0.04–9.6 mg/L and the absolute value of absorbance, and the detection limit and the quantitation limit were 0.024 mg/L and 1.29 mg/kg, respectively. There was a linear relationship between the concentration of sunset yellow in the range of 0.04–6.3 mg/L and the absorbance, the detection limit and the quantitation limit were 0.031 mg/L and 1.68 mg/kg, respectively. The spiked recoveries of tartrazine and sunset yellow in real samples were 97.0%–104% and 97.3%–103%, respectively, with relative standard deviations (n = 5) of 1.5%–2.6% and 1.2%–2.6%, respectively. The method was simple and rapid, and it could be used for the determination of tartrazine and sunset yellow in beverages with satisfactory results.

Key words: ethyl violet; tartrazine; sunset yellow; absorption spectrometry; acidity control

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