Catalytic spectrophotometric determination of trace molybdenum in natural- and tap-water samples.
Susumu Kawakubo, Kiyoshi Ogihara, Masaaki Iwatsuki
Abstract
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Susumu Kawakubo, Kiyoshi Ogihara, Masaaki Iwatsuki
Abstract
Open-access reader
A sensitive and simple catalytic spectrophotometric method for the determination of molybdenum has been developed using the molybdenum-catalyzed oxidation of L-ascorbic acid with hydrogen peroxide in the presence of ο-phenylenediamine to produce quinoxaline derivatives. The absorbance of the solution was measured at 340 nm for the determination of molybdenum after reacting for 5 min at pH 3.2 and 25°C and readjusting the pH of the solution to 1 with hydrochloric acid to stop the reaction. The calibration graph was, linear up to 4 ng/ml of molybdenum. The detection limit was 0.03 ng/ml (0.2 ng). The proposed method was successfully applied to river-, rain- and tap-water samples.
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A sensitive and simple catalytic spectrophotometric method for the determination of molybdenum has been developed using the molybdenum-catalyzed oxidation of L-ascorbic acid with hydrogen peroxide in the presence of ο-phenylenediamine to produce quinoxaline derivatives. The absorbance of the solution was measured at 340 nm for the determination of molybdenum after reacting for 5 min at pH 3.2 and 25°C and readjusting the pH of the solution to 1 with hydrochloric acid to stop the reaction. The calibration graph was, linear up to 4 ng/ml of molybdenum. The detection limit was 0.03 ng/ml (0.2 ng). The proposed method was successfully applied to river-, rain- and tap-water samples.
Key concepts: Tap water, Molybdenum, Detection limit, Absorbance, Hydrochloric acid, Chemistry, Ascorbic acid, Catalysis