蔡展帆,张佩霞,章锦涵,胡文敏,高 齐,周忆莲,林辉焕,熊 欣,梁旭霞.微波消解-电感耦合等离子体发射光谱法测定食品中锡含量的方法研究[J].食品安全质量检测学报,2020,11(16):5391-5397
微波消解-电感耦合等离子体发射光谱法测定食品中锡含量的方法研究
Research on determination of tin in food by inductively coupled plasma optical emission spectroscopy with microwave digestion
投稿时间:2020-06-01  修订日期:2020-08-12
DOI:
中文关键词:    盐酸  微波消解  电感耦合等离子发射光谱法
英文关键词:tin  hydrochloric acid  microwave digestion  inductively coupled plasma optical emission spectroscopy
基金项目:食品安全国家标准制定、修订项目(spaq-2019-027)、国家重点研发计划项目(2019YFC1606305)
作者单位
蔡展帆 广东省食品检验所 
张佩霞 广东省食品检验所 
章锦涵 广东省食品检验所 
胡文敏 广东省食品检验所 
高 齐 广东省食品检验所 
周忆莲 广东省食品检验所 
林辉焕 广东省食品检验所 
熊 欣 广东省食品检验所 
梁旭霞 广东省食品检验所 
AuthorInstitution
CAI Zhan-Fan Guangdong Institute of Food Inspection 
ZHANG Pei-Xia Guangdong Institute of Food Inspection 
ZHANG Jin-Han Guangdong Institute of Food Inspection 
HU Wen-Min Guangdong Institute of Food Inspection 
GAO Qi Guangdong Institute of Food Inspection 
ZHOU Yi-Lian Guangdong Institute of Food Inspection 
LIN Hui-Huan Guangdong Institute of Food Inspection 
XIONG Xin Guangdong Institute of Food Inspection 
LIANG Xu-Xia Guangdong Institute of Food Inspection 
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中文摘要:
      目的 建立微波消解-电感耦合等离子体发射光谱法(inductively coupled plasma optical emission spectroscopy, ICP-OES)测定食品中锡含量的方法。方法 采用5 mL硝酸+1 mL盐酸的酸体系对样品进行微波消解前处理, 并在90 ℃下赶酸, 再用电感耦合等离子发射光谱法以189.925 nm为分析谱线, 测定食品中锡含量。结果 该方法线性范围为0.01~ 5.00 mg/L, 相关系数大于0.999。方法检出限为0.7 mg/kg, 方法定量限为2.4 mg/kg, 多种基质样品的结果相对标准偏差<5%, 加标回收率在100.2%~109.4%。结论 该方法操作简便快捷, 结果准确, 精密度高, 灵敏度高, 干扰少, 适用于食品中锡的分析。
英文摘要:
      Objective To establish a method for the determination of tin in food by microwave digestion-inductively coupled plasma optical emission spectrometry (ICP-OES). Methods The samples were pretreated with 5 mL nitric acid and 1 mL hydrochloric acid before microwave digestion. The samples were driven out of acid at 90 ℃, and then the content of tin in food was determined by ICP-OES with 189.925 nm as the analytical line. Results The linear range of this method was 0.01–5.00 mg/L with correlation coefficient greater than 0.999. The method detection limit was 0.7 mg/kg, the quantification limit was 2.4 mg/kg. The relative standard deviation of the results of multiple matrix samples was less than 5%, and the spike recovery was 100.2%-109.4%. Conclusion The method is simple to operate, with accurate results, high precision, high sensitivity and less interference, and is suitable for the analysis of tin in food.
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