1981
DOI: 10.1039/an9810600243
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Spectrophotometric determination of nitrite in waters

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1983
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Cited by 28 publications
(4 citation statements)
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“…The molar absorptivity is 4.6 ϫ 10 4 liters mol Ϫ1 cm Ϫ1 (while the Sandell sensitivity is 0.0010 g cm Ϫ2 for an absorbance of 0.001) for determining nitrite. This is greater than the values obtained using Flamerz and Bashir's two methods (4,5), which are E max ϭ 1.47 ϫ 10 4 and 3.05 ϫ 10 4 , respectively, and Bajic and Jaselskis' method (6), E max ϭ 4.21 ϫ 10 4 , and the value about equals the best literature value (7) (6 -12): NO 2 Ϫ alone is determined, and sequential determination of the two ions can be performed without eliminating mutual interference or performing separation beforehand.…”
Section: Resultscontrasting
confidence: 74%
“…The molar absorptivity is 4.6 ϫ 10 4 liters mol Ϫ1 cm Ϫ1 (while the Sandell sensitivity is 0.0010 g cm Ϫ2 for an absorbance of 0.001) for determining nitrite. This is greater than the values obtained using Flamerz and Bashir's two methods (4,5), which are E max ϭ 1.47 ϫ 10 4 and 3.05 ϫ 10 4 , respectively, and Bajic and Jaselskis' method (6), E max ϭ 4.21 ϫ 10 4 , and the value about equals the best literature value (7) (6 -12): NO 2 Ϫ alone is determined, and sequential determination of the two ions can be performed without eliminating mutual interference or performing separation beforehand.…”
Section: Resultscontrasting
confidence: 74%
“…It was then utilized to determine the following chemical components: -Nitrate nitrogen (ppm) was determined spectrophotometrically at 410 nm according to the procedure of Cataldo et al (1975). -Nitrite nitrogen (ppm) was determined spectrophotometrically at 520 nm according to the procedure adopted by Flamerz and Bashir (1981).…”
Section: Chemical Analysismentioning
confidence: 99%
“…4 Numerous spectrophotometric methods based on the Griess-Ilosvay reaction have been proposed for nitrite determination. [5][6][7][8][9] This reaction involves the diazotization of the nitrite with an aromatic amine in acidic medium to form a diazonium salt, which by an aromatic electrophilic substitution (coupling reaction) with a phenolic compound or an aromatic amine leads to the formation of an azo dye. Shinn's proposal 10 to use sulfanilamide and N-(1-naphthyl)ethylenediamine dihydrochloride as diazotization and coupling reaction reagents, respectively, has been the basis of many FIA spectrophotometric methods.…”
Section: Introductionmentioning
confidence: 99%