Please use this identifier to cite or link to this item:
http://localhost:8080/xmlui/handle/123456789/2140
Title: | Determination of selenium(IV) after co-precipitation with Fe-Ti layered double hydroxides |
Authors: | Prasad, K Rao, K S Mary Gladis, J Naidu, G R K Prasada Rao, T |
Keywords: | Selenium(IV) Preconcentrative separation Layered double hydroxides Atomic-absorption spectrometry Ultra trace amounts Physicochemical properties Online preconcentration Lanthanum hydroxide |
Issue Date: | 2006 |
Publisher: | Polskie Towarzystwo Chemiczne-Polish Chemical Society |
Citation: | Chemia Analityczna 51(4):613-622;Jul-Aug 2006 |
Abstract: | The narrow margin between beneficial and toxic properties of selenium requires precise analytical methods for its fast and reliable determination. We have developed a precise co-precipitative preconcentration and separation procedure for SeO32- in the pH range 4.0-6.0 using Fe-Ti layered double hydroxides prepared from synthetic solutions of Fe(III) and Ti(IV), and industrial effluent. The obtained layered double hydroxide co-precipitant with SeO32- was dissolved in 2 mol L-1 H2SO4 and concentration of selenium was determined 3 spectrophotometrically. Calibration plot was linear over the concentration range of selenium (IV) 1-100 mu g L-1. Detection limit (S/N = 3) for selenium(IV) was 1.0 mu g L-1. Relative standard deviation for 5 mu g L-1 of the analyte was 3.0% (n = 5). The accuracy of the developed method was tested by analyzing certified reference materials of marine sediment (MESS-3) and soil (IAEA-Soil 7). Further-more, the developed procedure has been successfully applied to the analysis of selenium(IV) in soil and river and marine sediment samples. |
URI: | http://ir.niist.res.in:8080/jspui/handle/123456789/2140 |
ISSN: | 0009-2223 |
Appears in Collections: | 2006 |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
2006_0087.PDF Restricted Access | 115.64 kB | Adobe PDF | View/Open Request a copy |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.