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作 者:王宽强 张旭龙[2] 马玲[1] 刘银[1] 彭秧[1]
机构地区:[1]新疆大学化学化工学院,新疆乌鲁木齐830046 [2]新疆出入境检验检疫局,新疆乌鲁木齐830063
出 处:《分析科学学报》2013年第5期660-664,共5页Journal of Analytical Science
基 金:国家自然科学基金(No.201147005);国家质检总局项目
摘 要:建立了超声萃取,高效液相色谱-串联质谱法测定食品包装材料中10种增塑剂的方法。以甲醇和0.1%的甲酸水溶液为流动相、梯度洗脱、正离子电离模式(ESI+)、多反应监测扫描(MRM)对10种增塑剂进行定性与定量分析。结果表明,10种增塑剂都有较好的线性关系(r>0.99),定量限(S/N=10)在3.0~0.5μg/L。该方法的回收率为71.63%~118.33%,相对标准偏差为0.15%~17.68%(n=6)。实验表明该方法检测速度快,灵敏度高,适合于食品包装材料中增塑剂的检测。Ultrasonic extraction-Ultraperformance liquid chromatography tandem mass spectrometry (UPLC-LC/LC) was established for the simultaneous determination of 10 plasticizers in food Packaging materials. Under the mode of positive elect-spray ionization (ESI+), multi-reaction monitoring (MRM) was adopted for qualitative and quantitative analysis of 10 plasticizers,using a mobile phase of methanol and 0.1% formic acid/water solution in the gradient mode. The results showed that 10 plasticizers have good linear relationships,and correlation coefficients(r) were all more than 0.99 with the quantification limits between 3.0-0.5 μg/L(S/N= 10). The average recoveries of 10 plasticizers at three spiked levels ranged from 71.63%-118.33% with relative standard deviations of 0. 15%-17.68%. The method was rapid,highly sensitive and was suitable for the determination of 10 plasticizers in food packaging materials.
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