Hafez M A, Khalifa M E
Chemistry Department, Faculty of Science, Mansoura University, El-Mansoura, Egypt.
Talanta. 1997 May;44(5):787-96. doi: 10.1016/s0039-9140(96)02106-6.
A rapid and simple general complexometric method was presented for the determination of lead, cadmium and thallium or mercury or arsenic(V) in laboratory synthesized mixtures similar to those of some ores, minerals and alloys of such metals. The precision and accuracy attainable in successive titrations of Pb(2+), Cd(2+) and Tl(3+) or Hg(2+) or AsO(3-)(4) (As(5+)) with 0.05 and/or 0.01 mol 1(-1) solutions of disodium ethylenediaminetetraacetate (Na(2)EDTA) and standard Pb(NO(3))(2) of the same concentration using Bromo-Cresol Orange (BCO) as a new metallochromic indicator with visual endpoint indication were studied. For the analysis of a three component mixtures of the aforementioned ions, Tl(3+) was at first directly titrated with Na(2)EDTA at pH 0.5-1 (HNO(3)) using BCO as indicator. At the thallium endpoint an excess of Na(2)EDTA was added and the pH was adjusted at pH approximately 4.8 using hexamine-HNO(3) buffer (solution A). The excess EDTA was back-titrated with standard solution of Pb(NO(3))(2). 1,10-Phenanthroline (1,10-phen) was added to release the EDTA combined with Cd(2+), while thiosemicarbazide (TSC) was used to liberate the EDTA from the mercury-EDTA chelate. To determine AsO(3-)(4) ion in such type of mixtures the pH of (solution A) was raised to a value of 10 using ammonia buffer. Excess standard Mg(2+) solution was added and the formed precipitate of MgNH(4)AsO(4) was separated, dissolved and its magnesium content equivalent to AsO(3-)(4) was determined complexometrically using Eriochrome Black-T (EBT) indicator. The interference caused by different anions, cations and organic acids was investigated. A comparison of the indicators BCO and Xylenol Orange (XO) for successive titration of the studied metal ions was carried out. The proposed successive titration method was applied successfully to some real samples of ores, minerals and alloys of the studied metal ions and the results were satisfactory and agreed with those obtained by AAS.
提出了一种快速简便的通用络合滴定法,用于测定实验室合成混合物中的铅、镉、铊或汞或砷(V),这些混合物类似于某些矿石、矿物以及此类金属的合金。研究了使用溴甲酚橙(BCO)作为新型金属显色指示剂,通过目视终点指示,用0.05和/或0.01 mol·L⁻¹乙二胺四乙酸二钠(Na₂EDTA)溶液和相同浓度的标准硝酸铅(Pb(NO₃)₂)对Pb²⁺、Cd²⁺和Tl³⁺或Hg²⁺或AsO₄³⁻(As⁵⁺)进行连续滴定所能达到的精密度和准确度。对于上述离子的三元混合物分析,首先在pH 0.5 - 1(HNO₃)条件下,以BCO为指示剂,用Na₂EDTA直接滴定Tl³⁺。在铊的终点处加入过量的Na₂EDTA,并用六亚甲基四胺 - HNO₃缓冲液(溶液A)将pH调节至约4.8。过量的EDTA用硝酸铅标准溶液进行回滴。加入1,10 - 菲啰啉(1,10 - phen)以释放与Cd²⁺结合的EDTA,同时使用硫代氨基脲(TSC)从汞 - EDTA螯合物中释放EDTA。为了测定此类混合物中的AsO₄³⁻离子,使用氨缓冲液将(溶液A)的pH提高到10。加入过量的标准Mg²⁺溶液,分离并溶解形成的MgNH₄AsO₄沉淀,并用铬黑T(EBT)指示剂通过络合滴定法测定其与AsO₄³⁻相当的镁含量。研究了不同阴离子、阳离子和有机酸引起的干扰。对用于连续滴定所研究金属离子的指示剂BCO和二甲酚橙(XO)进行了比较。所提出的连续滴定法成功应用于一些所研究金属离子的矿石、矿物和合金的实际样品,结果令人满意,且与原子吸收光谱法(AAS)获得的结果一致。