On the spectrophotometric determination of with 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol

1988 ◽  
Vol 66 (3) ◽  
pp. 401-405 ◽  
Author(s):  
Lumír Sommer ◽  
Eva Šamlotová

2-(5-Bromo-2-pyridylazo)-5-diethylaminophenol (5-Br-PADAP) is a suitable reagent for the spectrophotometric determination of uranium but results are easily influenced by the reaction conditions as well as various common ions and masking agents. Optimum conditions, which must be carefully maintained, are 30% (v/v) dimethylformamide, 0.1% triton X-100, ≥ 8 × 10−5 M 5-Br-PADAP, 8 × 10−2 M triethanolamine, 7 × 10−3 M sodium fluoride, 10−2 M 5-sulphosalicylic acid, and 579 nm. Sodium sulphate (10−2 M) and CDTA (5.7 × 10−3 M) may serve as additional masking agents. A previous separation of uranium by extraction with 0.1 M tri-n-octylamine in benzene from 4 M HCl and re-extraction of 0.3 M HCl is recommended for analysis of natural water samples.

2013 ◽  
Vol 316-317 ◽  
pp. 279-285
Author(s):  
Xin Rong Wen ◽  
Chang Qing Tu

The paper presents a novel method for the separation/enrichment of trace Co2+ using microcrystalline phenolphthalein modified with 8-hydroxyquinoline (HQ) prior to the determination by spectrophotometry. The effects of different parameters,such as the dosages of phenolphthalein and HQ,various salts and acidity on the enrichment yield of Co2+ have been investigated to select the experimental conditions. The possible enrichment mechanism of Co2+ was discussed.The results showed that under the optimum conditions, Co2+ could be quantificationally adsorbed on the surface of microcrystalline phenolphthalein in the form of the chelate precipitate of Co(HQ)2 ,while K+,Na+,Ca2+,Mg2+,Cd2+,Zn2+,Mn2+,Fe2+ and Al3+ could not be adsorbed at all.Therefore,Co2+ was completely separated from the above metal ions in the solution. A new method for the spectrophotometric determination of trace cobalt after separation/enrichment using microcrystalline phenolphthalein modified with 8-hydroxyquinoline was established.The proposed method has been successfully applied to the determination of Co2+ in various environmental water samples, and the results agreed well with those obtained by FAAS method.


2019 ◽  
Vol 24 (1) ◽  
pp. 74 ◽  
Author(s):  
Bassima A. Abed Al-Hadi

In this research, an easy, acurate and rapid spectrophotometric method for determination of sulphite and thiamine hydrochloride is described. This method used proton transfer reaction between sulphite ion with alizarine at (pH 6.73) to develop red colour adduct that bears maximum absorption at 524 nm. This method was developed to determination of thiamine hydrochloride by bleaching the red colour (alizarine-sulphite product) at the optimum conditions established for the determination of sulphite. Beer’s law is obeyed in the concentration range (10-1000) μg/25ml (0.4-40) of sulphite and 10-1500, μg/25ml (0.4-60) for thiamine hydrochloride at the selected wavelength, the molar absorbtivity 2.6×104 l.mol-1.cm-1 for SO32- and 3.37×104 l.mol-1.cm-1 for thiamine hydrochloride, Sandell's index for sensitivity 0.00307 μg .cm-2 for sulphite  and 0.0100 μg .cm-2  for B1, the precision (RSD) of the method is ±0.23- ± 0.51% sulphite and ±0.15- ±0.25 thiamine hydrochloride. Good recoveries of sulphite and thiamine hydrochloride from water samples and pharmaceutical formation are achieved using the proposed method.   http://dx.doi.org/10.25130/tjps.24.2019.012


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