Article

Solvent extraction-spectrophotometric determination of phosphate with molybdate and malachite green in river water and sea-water.

Department of Chemistry, Faculty of Science, Okayama University, Tsushimanaka, Okayama-shi, Japan.
Talanta (impact factor: 3.79). 05/1984; 31(4):235-40. DOI:10.1016/0039-9140(84)80269-6 pp.235-40
Source: PubMed

ABSTRACT Molybdophosphate, formed between orthophosphate and molybdate in sulphuric acid solution, is extracted into a mixture of toluene and 4-methylpentan-2-one (1:3 v v ) with Malachite Green as counter-ion. A single extraction with equal phase volumes gives an apparent molar absorptivity for phosphate of 2.3 x 10(5) l.mole(-1).cm(-1) at 630 nm; the absorbance of the reagent blank is 0.03. With an organic to aqueous phase-volume ratio of 1:10, the molar absorptivity is 2.5 x 10(5) l.mole(-1).cm(-1) and the absorbance of the reagent blank 0.08. By the proposed method, ng ml levels of phosphorus can be determined, and the detection limit is about 0.1 ng ml . The standard deviation and relative standard deviation for the determination of phosphorus in tap water (4.3 ng ml ) are 0.05 ng ml and 1.1%, respectively. The method can also be applied to the determination of phosphorus in river water and sea-water.

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Keywords

apparent molar absorptivity
 
aqueous phase-volume ratio
 
counter-ion
 
detection limit
 
equal phase volumes
 
Malachite Green
 
molar absorptivity
 
Molybdophosphate
 
ng ml levels
 
proposed method
 
reagent blank
 
reagent blank 0.08
 
relative standard deviation
 
sea-water
 
single extraction
 
standard deviation
 
sulphuric acid solution
 

S Motomizu