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作 者:张孝松[1] 储著银[1] 徐霁昀[1] 林明[1] 林长山[1]
机构地区:[1]中国科学技术大学应用化学系
出 处:《色谱》1996年第5期397-399,共3页Chinese Journal of Chromatography
摘 要:在化学键合固定相ODS柱上,用Fe(Phen)_3^(2+)作流动相添加剂分离并用间接光度法检测无机阴离子。探讨了主要因素(如流动相中Fe(Phen)_3^(2+)浓度、有机溶剂浓度、pH值和离子强度等)对阴离子保留和检测灵敏度的影响。Cl~-,Br~-,NO_3~-和I~-具有良好的分离度;间接光度检测波长为Fe(Phen)_3^(2+)的最大吸收波长510nm。测定这4个离子的校正曲线的线性范围为1~160mg/L(Cl~-,Br~-,NO_3~-)和2~320mg/L(I~-);相关系数均达0.996。检测限(以S=2N计)分别为1.0ng(Cl~-),1.7ng(Br~-),1.9ng(NO_3~-)和5.6ng(I~-)。方法应用于雨水和自来水中Cl~-的测定,并获得满意的结果。Fe(Phen)3SO4 was used as a mobile phase additive for the liquid chromatographic separation of inorganic analyte anions on a Zorbax ODS column (250mm×4. 6mm i. d. ). The effects of organic modifier, concentration of Fe(Phen)3SO4, pH value and ionic strength in the mobile phase on the retention times and detection sensitivities of analyte anions had been investigated. The excellent resolution for CI, Br, NO3 and I using the mobile phase containing 1.0 ×1 0-4mol/L Fe (Phen)3SO4 at a flow rate of 1.0mL/min. Indirect photometric detection was used to detect the analyte anions by monitoring the eluate at 510nm where Fe (Phen) exhibits absorption maximum. The calibration graphs were linear over 1-160mg/L for Cl, Br and NO3, and 2-320mg/L for I. The detection limits were 1.0, 1.7, 1.9 and 5.6ng for CI, Br, NO, and I respectively.The proposed method has been applied to analyze rain and tap water and satisfactory results have been obtained.
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