化学通报(网络版)
化學通報(網絡版)
화학통보(망락판)
Chemistry Online
2004年
1期
,共1页
贺闰娟%钱春燕%朱若华*%谷学新
賀閏娟%錢春燕%硃若華*%穀學新
하윤연%전춘연%주약화*%곡학신
钯 2-(5-氯-2-吡啶)偶氮-5-二甲氨基苯胺(5-Cl-PADMA)%富集%石墨炉原子吸收法(GFAAS)
鈀 2-(5-氯-2-吡啶)偶氮-5-二甲氨基苯胺(5-Cl-PADMA)%富集%石墨爐原子吸收法(GFAAS)
파 2-(5-록-2-필정)우담-5-이갑안기분알(5-Cl-PADMA)%부집%석묵로원자흡수법(GFAAS)
Palladium%2-(5-Chloro-2-pyridylazo)-5-dimethylaminoaniline(5-Cl-PADMA)%Separation%Graphite furnace atomic absorption spectrometry (GFAAS)
强酸性条件下,钯(Ⅱ)与2-[(5-氯-2-吡啶)偶氮]-5-二甲氨基苯胺(5-Cl-PADMA)及溴化十六烷基三甲铵(CTMAB)可生成络合物,络合物经0.22m m孔径的混合纤维素膜富集后,用小体积的混合有机溶剂(乙二醇单甲醚和N,N-二甲基甲酰胺)溶解,加入一定量的混合基体改进剂(抗坏血酸和氯化铵)后,用石墨炉原子吸收法(GFAAS)测定其中的钯含量.实验结果表明,钯含量在0.2~2.3ng/mL和2.3~7ng/mL范围内线性关系良好,检出限为0.03ng/mL,用于矿石、土壤样品中痕量钯的测定,结果令人满意.
彊痠性條件下,鈀(Ⅱ)與2-[(5-氯-2-吡啶)偶氮]-5-二甲氨基苯胺(5-Cl-PADMA)及溴化十六烷基三甲銨(CTMAB)可生成絡閤物,絡閤物經0.22m m孔徑的混閤纖維素膜富集後,用小體積的混閤有機溶劑(乙二醇單甲醚和N,N-二甲基甲酰胺)溶解,加入一定量的混閤基體改進劑(抗壞血痠和氯化銨)後,用石墨爐原子吸收法(GFAAS)測定其中的鈀含量.實驗結果錶明,鈀含量在0.2~2.3ng/mL和2.3~7ng/mL範圍內線性關繫良好,檢齣限為0.03ng/mL,用于礦石、土壤樣品中痕量鈀的測定,結果令人滿意.
강산성조건하,파(Ⅱ)여2-[(5-록-2-필정)우담]-5-이갑안기분알(5-Cl-PADMA)급추화십륙완기삼갑안(CTMAB)가생성락합물,락합물경0.22m m공경적혼합섬유소막부집후,용소체적적혼합유궤용제(을이순단갑미화N,N-이갑기갑선알)용해,가입일정량적혼합기체개진제(항배혈산화록화안)후,용석묵로원자흡수법(GFAAS)측정기중적파함량.실험결과표명,파함량재0.2~2.3ng/mL화2.3~7ng/mL범위내선성관계량호,검출한위0.03ng/mL,용우광석、토양양품중흔량파적측정,결과령인만의.
A method for the preconcentration and determination of trace Pd(II) by graphite furnace atomic absorption spectrometry (GFAAS) was described. It was based on the formation of Pd(II)-2-(5-chloro-2-pyridylazo)-5-dimethylaminoaniline (5-Cl-PADAM)-exadecyltrimethylammonium bromide (CTMAB) complex in heavy acid medium. The complex was collected on a soluble membrane filter and the detection of the solution obtained after dissolving and analyzing the membrane in a proper solvent. The conditions for the formation and collection of the complex including pH, effect of surfactants, aperture of the membrane filter, effect of matrix modifiers etc. were optimized. Under the optimized conditions, the linear range was found in the range of 0.2~2.3ng× mL-1 and 2.3~7ng× mL-1 with the R=99.95% and R=99.98% respectively. The limit of detection achieved was 0.03ng× mL-1 after separation. The method was used for the determination of the soil and ore samples with satisfaction.