A simple, rapid and accurate complexometric method for the determination of palladium(II) is proposed, based on the selective demasking property of 2-mercapto propionyl glycine (MPGH<inf>2</inf>) towards palladium(II). In the presence of diverse metal ions, palladium(II) is complexed with excess of EDTA and the surplus EDTA is back titrated at pH 5-5.5 (acetic acid-acetate buffer) with standard zinc sulphate solution using xylenol orange as indicator. An excess of a 0.2% aqueous solution of MPGH<inf>2</inf> is then added to displace EDTA from Pd(II)-EDTA complex. The released EDTA is titrated with the same standard zinc sulphate solution as before. Reproducible and accurate results are obtained in the concentration range 2-22 mg of palladium with relative error of ±0.36% and coefficient of variation (n=6) not exceeding 0.31%. The effect of diverse ions are studied. The method is used for the determination of palladium in its complexes, catalysts and synthetic alloy mixtures.

dc.contributor.authorShetty, P.
dc.contributor.authorNityananda Shetty, A.N.
dc.contributor.authorGadag, R.V.
dc.date.accessioned2026-02-05T11:00:30Z
dc.date.issuedComplexometric determination of palladium(II) using 2-mercapto propionyl glycine as demasking agent
dc.description.abstract2002
dc.identifier.citationIndian Journal of Chemical Technology, 2002, 9, 2, pp. 127-129
dc.identifier.issn0971457X
dc.identifier.urihttps://idr.nitk.ac.in/handle/123456789/27994
dc.subjectedetic acid
dc.subjectglycine derivative
dc.subjectpalladium
dc.subjecttiopronin
dc.subjectzinc sulfate
dc.subjectaccuracy
dc.subjectanalytic method
dc.subjectanalytical error
dc.subjectarticle
dc.subjectcomplex formation
dc.subjectconcentration response
dc.subjectreproducibility
dc.titleA simple, rapid and accurate complexometric method for the determination of palladium(II) is proposed, based on the selective demasking property of 2-mercapto propionyl glycine (MPGH<inf>2</inf>) towards palladium(II). In the presence of diverse metal ions, palladium(II) is complexed with excess of EDTA and the surplus EDTA is back titrated at pH 5-5.5 (acetic acid-acetate buffer) with standard zinc sulphate solution using xylenol orange as indicator. An excess of a 0.2% aqueous solution of MPGH<inf>2</inf> is then added to displace EDTA from Pd(II)-EDTA complex. The released EDTA is titrated with the same standard zinc sulphate solution as before. Reproducible and accurate results are obtained in the concentration range 2-22 mg of palladium with relative error of ±0.36% and coefficient of variation (n=6) not exceeding 0.31%. The effect of diverse ions are studied. The method is used for the determination of palladium in its complexes, catalysts and synthetic alloy mixtures.

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