Simultaneous determination of eight additives in polymer food packaging materials by ultra-performance liquid chromatography-electrospray ionization tandem mass spectrometry

被引:0
|
作者
Zhang Xulong [1 ,3 ]
Liu Yin [2 ]
Gong Zhiguo [3 ]
Wang Pengju [2 ]
Wang Jide [1 ]
Feng Shun [1 ]
机构
[1] Xinjiang Univ, Coll Chem & Chem Engn, Minist Educ & Xinjiang Uyghur Autonomous Reg, Key Lab Oil & Gas Fine Chem, Urumqi 830046, Peoples R China
[2] Korla Entry Exit Inspect & Quarantine Bur, Korla 841000, Peoples R China
[3] Xinjiang Entry Exit Inspect & Quarantine Bur, Tech Ctr, Urumqi 830063, Peoples R China
关键词
ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS); additives; food packaging materials; polymer;
D O I
10.3724/SP.J.1123.2014.05038
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was proposed for the simultaneous determination of eight additives (Irgafos 168 (tri(2.4-di-tert-butylphenyl)phosphite), Irganox 1076 (octadecy1-beta-(4-hydroxy-3, 5-di-tert-butyl-phenyl) propionate), Irganox 1010 (pentaerythritol tetrakys 3-(3,5-di-tert-buty14-hydroxyphenyl)propionate), BHA (butyl hydroxy anisole) , TBHQ (tertiary butylhydroquinone), PG (propyl gallate), DG (dodecyl gallate) , UV-326 (2-(2'-hydroxy1-3'-tert-buty1-5'methylpheny1)-5-chlorobenzotriazole) in food packaging materials. After extracted by chloromethane through ultrasonic extraction, the samples were analyzed by UPLC-MS/MS. The chromatographic conditions were optimized, and the best separation was obtained on a Waters BEH-C18 column (50 mmx2.1 mm, 1.7 mu m) with gradient elution of 0.05% acetic acid solution and methanol. The analysis was performed by UPLC-MS/MS with electrospray ionization (ESI) source in switching between the positive and negative ion modes in one run for multiple reaction monitoring. The eight additives showed good linear relationships in the ranges with all the correlation coefficients (R-2) more than 0.993. The limits of detection (LODs, S/N = 3) and limits of quantitation (LOQs, S/N = 10 ) of this method were 0.13-5. 50 mu g/L and 0.45-17. 50 mu g/L, respectively. The recoveries were in the range of 63. 9% -127.0% with all the RSDs 15. 8% (n = 6). This method is simple, accurate and effective for the analysis of the eight additives in food packaging materials.
引用
收藏
页码:827 / 831
页数:5
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