Determination of nitrate in environmental water samples by conversion into nitrophenols and solid phase extraction-spectrophotometry, liquid ... [An article from: Analytica Chimica Acta]
Description
This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in 2004. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
Conversion of nitrate into a nitro-phenol derivative by reaction with 2-methylphenol or 2,6-dimethylphenol allowed at least 100-fold enrichment of the derivative on Lichrolut EN polymeric cartridge, and it is stable for up to 1 month on the cartridge. The derivative could be eluted with ammonia-methanol mixture. This reaction for nitrate determination has permitted a choice of final measurement by UV-Vis spectrophotometry, liquid chromatography or gas chromatography-mass spectrometry when the limits of detection were 10, 6 and 3@mgl^-^1, respectively, and the calibration range 20@mg to 10mgl^-^1 nitrate. The method has been validated by spiking natural water samples, when the recovery of nitrate was 98.5-108.4% (relative standard deviation 2.5-6.1%).
Description:
Conversion of nitrate into a nitro-phenol derivative by reaction with 2-methylphenol or 2,6-dimethylphenol allowed at least 100-fold enrichment of the derivative on Lichrolut EN polymeric cartridge, and it is stable for up to 1 month on the cartridge. The derivative could be eluted with ammonia-methanol mixture. This reaction for nitrate determination has permitted a choice of final measurement by UV-Vis spectrophotometry, liquid chromatography or gas chromatography-mass spectrometry when the limits of detection were 10, 6 and 3@mgl^-^1, respectively, and the calibration range 20@mg to 10mgl^-^1 nitrate. The method has been validated by spiking natural water samples, when the recovery of nitrate was 98.5-108.4% (relative standard deviation 2.5-6.1%).
