Citation:
ZHANG Haijing, LIN Shaobin. Determination of eight bisphenol diglycidyl ethers in water by solid phase extraction-high performance liquid chromatography-tandem mass spectrometry[J]. Chinese Journal of Chromatography,
;2014, 32(7): 730-734.
doi:
10.3724/SP.J.1123.2014.02026
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A solid phase extraction coupled with high performance liquid chromatography-tandem mass spectrometry (SPE-HPLC-MS/MS) method was developed for the determination of eight bisphenol diglycidyl ethers, including bisphenol A diglycidyl ether (BADGE), bisphenol A (3-chloro-2-hydroxypropyl) glycidyl ether(BADGE·5HCl), bisphenol A bis(3-chloro-2-hydroxypropyl) ether(BADGE·52HCl), bisphenol A (2,3-dihydroxypropyl) glycidyl ether(BADGE·5H2O), bisphenol A bis(2,3-dihydroxypropyl) ether(BADGE·52H2O), bisphenol A (3-chloro-2-hydroxypropyl) (2,3-dihydroxypropyl) ether(BADGE·5HCl·5H2O), bisphenol F diglycidyl ether(BFDGE) and bisphenol F bis(3-chloro-2-hydroxypropyl) ether(BFDGE·52HCl) in water. A total of ten samples were collected from the leaching of the coatings for drinking water supply system. Then, 200 mL exposure water was preconcentrated on C18 solid-phase extraction cartridge. The eight compounds were analyzed by liquid chromatography-tandem mass spectrometry method on a C18 column by the gradient elution with methanol, water and 5 mmol/L ammonium acetate as mobile phases in the multiple reaction monitoring (MRM) scan mode. The external matrix standard solutions were used for the quantitative determination and the calibration curves of the eight compounds showed good linearity in the range of 0.007-5.00 μg/L with the correlation coefficients more than 0.9990. The limits of quantification (LOQs) of the method were 7-91 ng/L. The spiked recoveries ranged from 79.1% to 101% with the relative standard deviations of 4.0%-12%. The method is sensitive and accurate, and is applicable to the determination of bisphenol diglycidyl ethers in water.
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