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作 者:杨晓慧[1] 杨龙虎[2] 霍燕燕[1] 马盛杰 翟云会[1] 韩权[1,2]
机构地区:[1]西安文理学院化学与化学工程学院,陕西西安710065 [2]延安大学化学与化工学院,陕西延安716000
出 处:《分析科学学报》2015年第1期107-110,共4页Journal of Analytical Science
基 金:西安市科技计划(No.CXY1352WL04);2013年西安市水务局横向项目
摘 要:以2-(5-溴-2-吡啶偶氮)-5-二甲氨基苯胺(5-Br-PADMA)为螯合剂,Triton X-114为萃取剂,建立了浊点萃取-石墨炉原子吸收光谱法测定超痕量Cu(Ⅱ)的新方法。研究了溶液pH、螯合剂和表面活性剂浓度、平衡温度和时间等因素对浊点萃取的影响。优化条件为:pH=5.0 HAc-NaAc缓冲溶液,0.35 mL 5.0×10-4 mol/L 5-BrPADMA,1.0mL 1.0%Triton X-114,60℃保温15min。方法的线性范围为0.05~4.0ng/mL,检出限为0.017ng/mL,相对标准偏差为3.1%(n=10),富集因子为48。方法用于水样中痕量Cu(Ⅱ)的测定,加标回收率在97.0%~102.0%之间。A new method based on cloud point extraction(CPE)and graphite furnace atomic absorption spectrometry(GFAAS)was established for the determination of ultra-trace Cu(Ⅱ)in water samples.2-(5-bromo-2-pyridylazo)-5-dimethylaminoaniline(5-Br-PADMA)was used as the chelating agent and Triton X-114 as the extractant.The main parameters affecting extraction,such as pH,concentration of chelating agent and surfactant,extraction temperature and time,were investigated in detail.The optimized CPE conditions were as follows:pH=5.0 HAc-NaAc buffer solution,0.35 mL 5.0×10-4mol/L 5-Br-PADMA,1.0 mL 1.0% Triton X-114,heat-assisted at 60 ℃ for 15 min.Under optimized conditions,the analytical curve was linear in the range of 0.05-4.0ng/mL and the detection limit was0.017ng/mL for Cu(Ⅱ),and relative standard deviation was 3.1%(c=0.1ng/mL,n=10),the enrichment factor was 48.The method has been applied to the determination of trace copper in water samples and the recovery were 97.0%-102.0%for the spiked tap water sample.
关 键 词:2-(5-溴-2-吡啶偶氮)-5-二甲氨基苯胺 Cu(Ⅱ) TRITON X-114 浊点萃取 石墨炉原子吸收光谱法
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