Spectrophotometric Determination of Nitrogen Dioxide in Air and Nitrite in Water And Soil Samples

1995 ◽  
Vol 28 (3) ◽  
pp. 535-554
Author(s):  
M. Pandurangappa ◽  
N. Balasubramanian
1994 ◽  
Vol 77 (6) ◽  
pp. 1639-1646 ◽  
Author(s):  
K Shanthi ◽  
N Balasubramanian

Abstract Dibenzoyl methane is introduced as a new coupling agent for the determination of nitrogen dioxide in air and for nitrite in water and soil samples. Nitrogen dioxide is fixed as nitrite in NaOH–sodium arsenite trapping solution and also in triethanoamine trapping solution. The method is based on the diazo coupling reaction of p-nitro aniline with a new coupling agent, dibenzoyl methane. The azo dye formed under aqueous alkaline condition has an absorption maximum at 520 nm and obeys Beer’s law over a range of 0–20 μg nitrite per 10 ml analyte. The dye formed is stable for 40 h. The relative standard deviation is 2.8% for 10 determinations at 10 μg nitrite per 10 ml analyte. The color system upon extraction with isobutyl methyl ketone–amyl alcohol (1+1) shows a λ max at 520 nm and a Beer’s law range of 0–4 μg nitrite. The developed color is stable for 7 h in the organic phase. The relative standard deviation is 3.0% for 10 determinations at 2 μg nitrite. The molar extinction coefficient of the color system is 3.6 × 104 L/(mol·cm). The effect of interfering gases and ions on the determination is described. The method was applied to the determination of residual amounts of nitrogen dioxide present in the laboratory fume cupboard and in automobile exhaust gas. The method was also applied to the determination of nitrite and nitrate in water and soil samples. The results obtained were compared with the standard sulfanilamide–NEDA (N-1 naphthyl ethylene diamine dihydrochloride) method. The method can be used to determine levels as low as 0.5 μg nitrite in aqueous medium and 0.1 μg nitrite upon extraction.


2016 ◽  
Vol 28 (8) ◽  
pp. 1861-1866 ◽  
Author(s):  
B. Natesh Kumar ◽  
S. Himagirish Kumar ◽  
G.G. Redhi ◽  
N.V.V. Jyothi

2007 ◽  
Vol 146 (1-2) ◽  
pp. 137-141 ◽  
Author(s):  
C. Sivani ◽  
G. Ramakrishna Naidu ◽  
J. Narasimhulu ◽  
D. Rekha ◽  
J. Dilip Kumar ◽  
...  

1997 ◽  
Vol 80 (6) ◽  
pp. 1308-1314 ◽  
Author(s):  
Wayne E Rae ◽  
Charles A Lucy

Abstract A capillary zone electrophoresis (CZE) method was developed to separate and determine chlorinated phenols in water and soil samples. A mixture of 16 chlorinated phenols was resolved in 25 min by using a 77 cm (70 cm to detector) × 75 μm fused silica capillary with 0.015M tetraborate/0.045M phosphate (pH 7.3) buffer at 22 kV. Calibration linearities for water samples in the low parts-permillion range were good (correlation coefficient > 0.99) for all solutes except p-chlorophenol. Average precision was 17% relative standard deviation. Typical detection limits were in the 200 μg/L range. Recoveries of chlorinated phenols from synthetic soil samples with methanol were quantitative.


2013 ◽  
Vol 25 (12) ◽  
pp. 6486-6490 ◽  
Author(s):  
N. Laitip ◽  
N. Chomnawang ◽  
N. Youngvises ◽  
W. Threeprom

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