Solvent extraction-spectrophotometric determination of boron with 3,5-di-tert-butylcatechol and ethyl violet

Boric acid and 3,5-di-tert-butylcathechol formed a complex anion at pH 6.3-8.7 which was extracted into toluene as an ion pair with ethyl violet (EV); the excess EV coextracted into toluene was removed by adding 3% hydrogen peroxide. Boron was determined spectrophotometrically by measuring the absor...

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Veröffentlicht in:Anal. Chem.; (United States) 1984-05, Vol.56 (6), p.948-950
Hauptverfasser: Oshima, Mitsuko, Motomizu, Shoji, Toei, Kyoji
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container_title Anal. Chem.; (United States)
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creator Oshima, Mitsuko
Motomizu, Shoji
Toei, Kyoji
description Boric acid and 3,5-di-tert-butylcathechol formed a complex anion at pH 6.3-8.7 which was extracted into toluene as an ion pair with ethyl violet (EV); the excess EV coextracted into toluene was removed by adding 3% hydrogen peroxide. Boron was determined spectrophotometrically by measuring the absorbance of EV of the ion pair in toluene at 610 nm. The calibration curve was linear within a range of 0.043 ..mu..g of boron, and the molar absorptivity was 10.5 x 10/sup 4/ L mol/sup -1/ cm/sup -1/. This method, using the new complexing agent, was applied to the determination of boron in seawater and found to be appreciably satisfactory compared with other methods. 7 references, 3 tables, 2 figures.
doi_str_mv 10.1021/ac00270a020
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Chem.; (United States)</title><addtitle>Anal. Chem</addtitle><description>Boric acid and 3,5-di-tert-butylcathechol formed a complex anion at pH 6.3-8.7 which was extracted into toluene as an ion pair with ethyl violet (EV); the excess EV coextracted into toluene was removed by adding 3% hydrogen peroxide. Boron was determined spectrophotometrically by measuring the absorbance of EV of the ion pair in toluene at 610 nm. The calibration curve was linear within a range of 0.043 ..mu..g of boron, and the molar absorptivity was 10.5 x 10/sup 4/ L mol/sup -1/ cm/sup -1/. 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Boron was determined spectrophotometrically by measuring the absorbance of EV of the ion pair in toluene at 610 nm. The calibration curve was linear within a range of 0.043 ..mu..g of boron, and the molar absorptivity was 10.5 x 10/sup 4/ L mol/sup -1/ cm/sup -1/. This method, using the new complexing agent, was applied to the determination of boron in seawater and found to be appreciably satisfactory compared with other methods. 7 references, 3 tables, 2 figures.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ac00270a020</doi><tpages>3</tpages></addata></record>
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ispartof Anal. Chem.; (United States), 1984-05, Vol.56 (6), p.948-950
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1520-6882
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source American Chemical Society Journals
subjects 400104 - Spectral Procedures- (-1987)
Analytical chemistry
AROMATICS
BORON
BORON COMPLEXES
CHEMICAL ANALYSIS
Chemistry
COMPLEXES
DATA
DEVELOPERS
ELEMENTS
Exact sciences and technology
EXPERIMENTAL DATA
EXTRACTION
HYDROGEN COMPOUNDS
HYDROXY COMPOUNDS
INFORMATION
INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY
NUMERICAL DATA
ORGANIC COMPOUNDS
OXYGEN COMPOUNDS
PHENOLS
POLYPHENOLS
PYROCATECHOL
QUANTITATIVE CHEMICAL ANALYSIS
SEAWATER
SEMIMETALS
SEPARATION PROCESSES
SOLVENT EXTRACTION
Spectrometric and optical methods
SPECTROPHOTOMETRY
WATER
title Solvent extraction-spectrophotometric determination of boron with 3,5-di-tert-butylcatechol and ethyl violet
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