P~ecisiorr. An estimate of the precision of this method was ascertained from the results of II samples, each containing 2.17 p.p.m. of vanadium. These samples gave a mean absorbance value of 0.468 at 323 nm. The standard deviation was 0.003 absorbance unit, or a relative standard deviation of 0.64(%
Direct titration of vanadium(IV) with EDTA using N-benzoyl-N-phenylhydroxylamine as metal indicator
โ Scribed by V.R.M. Kaimal; S.C. Shome
- Publisher
- Elsevier Science
- Year
- 1962
- Tongue
- English
- Weight
- 244 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0003-2670
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โฆ Synopsis
SHOriT_ COMtiUNlGATlONS in benzenei2. From the aqueous phase, nickel is extracted as usual aMer,.evaporation of the acid and adjustment to PH 6.0.
Recommended
@ocedure. To an aqueous solution containing 180-1600 pg of nickel in a separatory funnel, add IO ml of buffer solution of pH 5.5-8.0 and extract as described under "General procedure".
From ten runs as above with 524 rug of nickel, the absorbance measured was,.. 0.155 -& 0.002 ; the standard deviation was f. I.oO/~ and the accuracy within & x.50/;'.*'.' The proposed method is simple and rapid (requiring 15 to 20 min per run) and at the same time shows good reproducibility and accuracy. The sensitivity is 0.14 pg of nickel per ml (Sandell's definition).
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