文章摘要
付善良,丁 利,肖家勇,龚 强,焦艳娜,王晓兵,王利兵.加速溶剂萃取-GC-MS法检测食品接触材料——纸、纸板、木材和木制品中的6种氯酚类物质残留[J].包装工程,2011,32(15):48-52.
FU Shan-liang,DING Li,XIAO Jia-yong,GONG Qiang,JIAO Yan-na,WANG Xiao-bing,WANG Li-bing.Determination of 6 Chlorophenols in Paper, Paperboard, Wood and Wood Products Used as Food Contact Materials by Accelerated Solvent Extraction and GC-MS[J].Packaging Engineering,2011,32(15):48-52.
加速溶剂萃取-GC-MS法检测食品接触材料——纸、纸板、木材和木制品中的6种氯酚类物质残留
Determination of 6 Chlorophenols in Paper, Paperboard, Wood and Wood Products Used as Food Contact Materials by Accelerated Solvent Extraction and GC-MS
投稿时间:2011-05-18  修订日期:2011-08-10
DOI:
中文关键词: 加速溶剂萃取  气相色谱-质谱  含氯酚
英文关键词: accelerated solvent extraction (ASE)  gas chromatography-mass spectrometry (GC-MS)  chlorophenols (CPs)
基金项目:
作者单位
付善良 湖南出入境检验检疫技术中心 食品安全科学技术湖南省重点实验室长沙 410004 
丁 利 湖南出入境检验检疫技术中心 食品安全科学技术湖南省重点实验室长沙 410004 
肖家勇 湖南出入境检验检疫技术中心 食品安全科学技术湖南省重点实验室长沙 410004 
龚 强 湖南出入境检验检疫技术中心 食品安全科学技术湖南省重点实验室长沙 410004 
焦艳娜 湖南出入境检验检疫技术中心 食品安全科学技术湖南省重点实验室长沙 410004 
王晓兵 中国石油和化学工业联合会,北京 100029 
王利兵 湖南出入境检验检疫技术中心 食品安全科学技术湖南省重点实验室长沙 410004 
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中文摘要:
      建立了检测食品接触材料——纸、纸板、木材和木制品中含氯酚(CPs)残留量的气相色谱-质谱(GC-MS)分析方法。采用加速溶剂萃取(ASE)法为样品前处理手段,优化了萃取溶剂、萃取温度、静态萃取时间、冲洗体积和萃取循环次数等实验参数。优化结果为:以二氯甲烷为萃取溶剂,萃取温度为150 ℃,静态萃取时间为10 min,冲洗体积为(占萃取罐体积的)60%,萃取循环次数为1次。结果表明:6种CPs在0.05~2.0 μg/mL质量浓度范围内具有良好的线性关系(R>0.99);平均回收率在86.8%~108.8%之间(n=6);〖JP3〗相对标准偏差(RSD)为1.8%~14.2%(n=6);方法的检测限为0.01 mg/kg。研究表明该方法高效、简便、快捷、灵敏、准确可靠,可用于实际样品的CPs残留量的监测。
英文摘要:
      A new analytical method was developed for the determination of CPs in paper, paperboard, wood and wood products used as food contact materials by accelerated solvent extraction (ASE) and gas chromatography-mass spectrometry (GC-MS). The operational parameters of ASE, such as extraction solvent, extraction temperature, static extraction time, flush volume and extraction cycles, were optimized. The optimized procedure was using dichloromethane as extraction solvent, 150 ℃ of extraction temperature, 10 min of static extraction time, and 60% flush volume; the extraction recoveries of 6 CPs were nearly to 100% for only one cycle. The results indicated that the developed method has good linearity (R>0.99) in 0.05~2.0 μg/mL mass concentration, good recoveries (86.8%~108.8%) and precision (relative standard deviation (RSD) 1.8%~14.2% ); the limited of detection (LOD) of the 6 CPs are 0.01 mg/kg. It was concluded that the developed method is efficient, simple, rapid, sensitive, accurate and reliable, which can be utilized for CPs residual inspection of sample.
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