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Catalytic Kinetic Spectrophotometric Determination of Trace Palladium (Ⅱ) with Poniacyl Carmine 2B

机译:氧化胭脂红2B催化动力学光度法测定痕量钯(Ⅱ)。

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A new sensitive and selective catalytic kinetic spectrophotometric method for the determination of trace amount of palladium (Ⅱ) has been developed. The method is based on the catalytic effects of palladium (Ⅱ) on the reduction reactions of Poniacyl Carmine 2B (PC 2B) by sodium dihydrogen hypophosphite (NaH2PO2) in sulfuric acid medium. The optimal reaction conditions are PC 2B (1.0×10-3 mol/L) 0.8 mL, H2SO4 (2.0 mol/L) 1.0 mL, NaH2PO2 (100 g/L) 3.0 mL and 18 min at 100℃. Under the condition selected, trace amounts of palladium (Ⅱ) can be determined. The linear ranges are 0.008~0.032 μg/mL of Pd(Ⅱ) with a detection limit of 5.51×10-10 g/mL. the relative standard deviation was less than 4.8% (n=11). The coexistent ions are eliminated by preconcentration and separation with sulphydryl dextran gel (SDG). The results were fairly satisfactory. The method has been applied to the determination of Pd(Ⅱ) in activator samples with satisfactory results.
机译:建立了一种灵敏,选择性催化动力学光度法测定痕量钯(Ⅱ)的新方法。该方法基于钯(Ⅱ)对次硫酸氢二钠(NaH2PO2)在硫酸介质中还原烟碱胭脂红2B(PC 2B)的催化作用。最佳反应条件为PC 2B(1.0×10-3 mol / L)0.8 mL,H2SO4(2.0 mol / L)1.0 mL,NaH2PO2(100 g / L)3.0 mL和在100℃下18分钟。在选择的条件下,可以测定痕量的钯(Ⅱ)。 Pd(Ⅱ)的线性范围为0.008〜0.032μg/ mL,检出限为5.51×10-10 g / mL。相对标准偏差小于4.8%(n = 11)。通过预浓缩并用巯基右旋糖酐凝胶(SDG)分离可消除共存离子。结果相当令人满意。该方法用于活化剂样品中Pd(Ⅱ)的测定,结果令人满意。

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