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dc.contributor.authorPrasad, K-
dc.contributor.authorPraveen, R S-
dc.contributor.authorPrasada Rao, T-
dc.contributor.authorGopikrishna, P-
dc.contributor.authorNaidu, G R K-
dc.date.accessioned2015-01-16T07:47:57Z-
dc.date.available2015-01-16T07:47:57Z-
dc.date.issued2005-
dc.identifier.citationAtomic Spectroscopy 26(5):173-181; 2005en_US
dc.identifier.issn0195-5373-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1768-
dc.description.abstractA procedure for chromium speciation prior to flame atomic absorption spectrometry (FAAS) detection is proposed. In this procedure, chromium(III) and chromium(VI) species were sequentially separated using an off-line batch coprecipitative preconcentration onto bivalent or trivalent metal-diethylammonium diethyl-dithiocarbamate (DDTC) collectors. This separation is based on the selective coprecipitation of chromium(III) onto a nickel-DDTC collector followed by coprecipitation of chromium(VI) onto a bismuth(III)-DDTC collector. The preconcentrated metal-DDTC collectors were dissolved in 5 mL of a 1:1 mixture of nitric acid and methanol. Linear calibration plots were obtained for both chromium(III) and chromium(VI) species in the concentration range of 0-200 mu g/L in the initial solution. A 200-fold enrichment of chromium(III) and chromiurn(VI) was observed with detection limits of 0.4 and 0.6 mu g L-1, respectively. Five replicate determinations of 20 mu g of chromium(III) and chromium(VI) present in a 1.0-L sample solution gave a relative standard deviation of 2.8 and 3.2%, respectively. The developed procedure has been successfully utilized for the estimation of chromium(III) and chromium(VI) in several tannery industry effluents.en_US
dc.language.isoenen_US
dc.publisherPerkin-Elmer Corporationen_US
dc.subjectFlame atomic absorption spectrometryen_US
dc.subjectChromium(III)en_US
dc.subjectChromium(VI)en_US
dc.subjectDiethylammonium diethyl-dithiocarbamateen_US
dc.titleSequential preconcentrative separation of Cr(VI) and Cr(III) species from tannery effluents and subsequent determination by flame AASen_US
dc.typeArticleen_US
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