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出 处:《分析化学》1996年第7期802-805,共4页Chinese Journal of Analytical Chemistry
基 金:四川省教委科研基金
摘 要:本文提出了极谱测定微量钯的钯-7-碘-8-羟基喹啉-5-磺酸(7-I-H2QS)新体系。在0.10mol/LHAc,5.0×10-5mol/L7-I-H2QS溶液中,在线性扫描示波极谱仪上,钯(Ⅱ)有一灵敏的络合物吸附波,峰电位为-0.54V(vs.SCE),波高与钯浓度在7.0×10-8~5。0×10-6mol/L范围内呈良好的线性关系。当含量更低时,在悬汞电极上用吸附溶出伏安法测定,它集时间为200s时,线性范围为1.9×10-9~9.9×10-8mol/L。检出限为3.8×10-10mol/L(38ng/L)。对极谱波性质进行了探讨,用于矿样中痕量钯的测定,结果满意。A new system of palladium-7-iodo-8-hydroxyquinolne-5-sulphonic anid (7-I-H2QS) for the determination of palladium by polarography has been proposed. In a solution of 0. 10 mol/L HAc and 5.0×10-5mol/L 7-I-H2QS, a sensitive adsorptive wave of palladi um-7-I-H2QS complex is obtained by linear-sweep polarography. The peak potential of the wave appears at -0. 54 V(vs. SCE). The change of peak height of derivative wave with con centration of palladium is linear in the range of 7. 0×10-8~5. 0×10-6mol/L. Using a hang ing mercury drop electrode for adsorptive stripping voltammetry and preconcentrating for 200 s, the calibration curve for palladium is linear in the range of 1. 9 × 10- 9~9. 9 ×10-8mol/L.The detection limit is 3. 8 × 10-10'mol/L (for a 10 min preconcentration time). The method has been successfully applied to the determination of palladium in mineral. The characteris tics of the polarographic wave has been investigated by several electrochemical methods.
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