RETRACTED: Development of novel reactions for the simple and sensitive spectrophotometric determination of vanadium in various samples.

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Inductively coupled plasma-optical emission spectrometry for on-line determination of multi trace elements in environmental samples after preconcentration by using Borassus flabellifer inflorescence loaded with 2-propylpiperidine-1-carbodithioate.

A procedure was developed for the determination of Cu, Mn, Pb, Cd, Co, Cr, and Zn in water samples by Inductively Coupled Plasma-Optical Emission Spectrometry (ICP-OES) after preconcentration on synthesized 2-propylpiperidine-1-carbodithioate supported by Borassus flabellifer Inflorescence (BFI). The sorbed element was subsequently eluted with 0.4 M HNO3, and the acid eluates were analyzed by ICP-OES.

Spectrophotometric determination with a chromogenic reagent of lead in vegetables.

A method was developed for the simple, selective, and sensitive spectrophotometric determination of lead in vegetables with synthesized chromogenic reagent 3-[(2,6-dibromo-4-methylphenyl)diazenyl]-4,5-dihydroxy-6-[(2,4,6-tribromophenyl)diazenyl]naphthalene-2,7-disulfonic acid (DBMTBA; 1). In 0.25 M phosphoric acid medium, which greatly increases the selectivity, lead reacts with DBMTBA to form a 1:2 blue complex, which shows maximum absorption at 646 nm.

Preconcentration technique for the determination of trace elements in natural water samples by ICP-AES.

A procedure was developed for the determination of Cd, Cu, Zn, Co, Ni, Mn, Pb and Mo in water samples by inductively coupled plasma atomic emission spectrometry (ICP-AES) after preconcentration on a morpholine dithiocarbamate (mor-DTC) supported by bagasse (Saccharam aphisinaram). The sorbed elements were subsequently eluted with 4,M HNO3 and the acid eluates were analysed by ICP-AES. The influence of various parameters such as pH, flow rate of sample, eluent concentration, volume of the sample and volume of eluent were investigated to enhance the sensitivity of the present method.

Studies of selenium in environmental samples and synthetic mixtures by spectrophotometry.

A rapid, highly sensitive and selective spectrophotometric method for the determination of traces of selenium(IV) is described. The method is based on oxidation of p-nitroaniline by selenium(IV) followed by coupling reaction with N-(1-naphthalene-1-yl)ethane-1,2-diamine dihydrochloride (NEDA) in neutral medium to give red colored derivative with lambda(max) 515 nm and is stable for more than 10 days at 35 degrees C. Beer's law is obeyed for selenium(IV) in the concentration range of 0.