Yu Li-Ping
Department of Chemistry, Tianjin University, Tianjin 300072, China.
J Agric Food Chem. 2005 Dec 14;53(25):9656-62. doi: 10.1021/jf051777k.
A cloud point extraction methodology was developed for simultaneous preconcentration of Hg(II), methylmercury (MeHg), ethylmercury (EtHg), and phenylmercury (PhHg) prior to reversed-phase high-performance liquid chromatography (HPLC) on-line coupled with cold vapor atomic fluorescence spectrometry for speciation analysis of mercury in fish. The four mercury species were taken into complexes with ammonium pyrrolidine dithiocarbamate (APDC) in aqueous nonionic surfactant Triton X-114 medium and concentrated in the surfactant-rich phase by bringing the solution to the temperature of 40 degrees C. Baseline separation of the enriched complexes was achieved on an RP-C(18) column with a mixture of methanol, acetonitrile, and water (65:15:20, v/v) containing 200 mmol L(-1) HAc (pH 3.5) as the mobile phase. An on-line postcolumn oxidation of the effluent from HPLC, in the presence of K2S2O8 in HCl, was applied in the system followed by an optimal cold vapor generation of mercury species. The variables affecting the complexation and extraction steps were examined. The preconcentration of 10 mL of solution with 0.08% w/v Triton X-114 and 0.04% w/v APDC at pH 3.5 gave enrichment factors of 29, 43, 80, and 98 for MeHg, EtHg, PhHg, and Hg(II), respectively. Low detection limits (S/N = 3) were obtained, ranging from 2 to 9 ng L(-1) (as Hg) for all species. The developed method was successfully applied to the speciation of mercury in real fish samples.
建立了一种浊点萃取方法,用于在反相高效液相色谱(HPLC)在线联用冷蒸气原子荧光光谱法对鱼类中的汞进行形态分析之前,同时预富集汞(II)、甲基汞(MeHg)、乙基汞(EtHg)和苯基汞(PhHg)。在水性非离子表面活性剂Triton X - 114介质中,这四种汞形态与吡咯烷二硫代氨基甲酸铵(APDC)形成络合物,并通过将溶液加热至40℃,使其在富含表面活性剂的相中富集。在RP - C(18)柱上,以甲醇、乙腈和水(65:15:20,v/v)的混合物为流动相,其中含有200 mmol L(-1) HAc(pH 3.5),实现了富集络合物的基线分离。在该系统中,对HPLC流出物在HCl存在下用K2S2O8进行在线柱后氧化,随后对汞形态进行最佳冷蒸气发生。研究了影响络合和萃取步骤的变量。在pH 3.5条件下,用0.08% w/v Triton X - 114和0.04% w/v APDC对10 mL溶液进行预富集,MeHg、EtHg、PhHg和Hg(II)的富集因子分别为29、43、80和98。所有形态的检测限均较低(S/N = 3),范围为2至9 ng L(-1)(以Hg计)。所建立的方法成功应用于实际鱼类样品中汞的形态分析。