A simplified approach to the determination of N-nitroso glyphosate in technical glyphosate using HPLC with post-derivatization and colorimetric detection
A simple and sensitive HPLC post-derivatization method with colorimetric detection has been developed for the determination of N-nitroso glyphosate in samples of technical glyphosate. Separation of the analyte was accomplished using an anionic exchange resin (2.50 mm × 4.00 mm i.d., 15 μm particle s...
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todo:paper_00399140_v72_n3_p1054_Kim2023-10-03T14:50:01Z A simplified approach to the determination of N-nitroso glyphosate in technical glyphosate using HPLC with post-derivatization and colorimetric detection Kim, M. Stripeikis, J. Iñón, F. Tudino, M. Glyphosate HPLC with post-derivatization N-nitrosoglyphosate Colorimetry Energy utilization High performance liquid chromatography Ion exchange Particle size Glyphosate N-nitrosoglyphosate Post-derivatization Nitrogen compounds A simple and sensitive HPLC post-derivatization method with colorimetric detection has been developed for the determination of N-nitroso glyphosate in samples of technical glyphosate. Separation of the analyte was accomplished using an anionic exchange resin (2.50 mm × 4.00 mm i.d., 15 μm particle size, functional group: quaternary ammonium salt) with Na2SO4 0.0075 M (pH 11.5) (flow rate: 1.0 mL min-1) as mobile phase. After separation, the eluate was derivatized with a colorimetric reagent containing sulfanilamide 0.3% (w/v), [N-(1-naphtil)ethilendiamine] 0.03% (w/v) and HCl 4.5 M in a thermostatized bath at 95 °C. Detection was performed at 546 nm. All stages of the analytical procedure were optimized taking into account the concept of analytical minimalism: less operation times and costs; lower sample, reagents and energy consumption and minimal waste. The limit of detection (k = 3) calculated for 10 blank replicates was 0.04 mg L-1 (0.8 mg kg-1) in the solid sample which is lower than the maximum tolerable accepted by the Food and Agriculture Organization of the United Nations. © 2007 Elsevier B.V. All rights reserved. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00399140_v72_n3_p1054_Kim |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
Glyphosate HPLC with post-derivatization N-nitrosoglyphosate Colorimetry Energy utilization High performance liquid chromatography Ion exchange Particle size Glyphosate N-nitrosoglyphosate Post-derivatization Nitrogen compounds |
spellingShingle |
Glyphosate HPLC with post-derivatization N-nitrosoglyphosate Colorimetry Energy utilization High performance liquid chromatography Ion exchange Particle size Glyphosate N-nitrosoglyphosate Post-derivatization Nitrogen compounds Kim, M. Stripeikis, J. Iñón, F. Tudino, M. A simplified approach to the determination of N-nitroso glyphosate in technical glyphosate using HPLC with post-derivatization and colorimetric detection |
topic_facet |
Glyphosate HPLC with post-derivatization N-nitrosoglyphosate Colorimetry Energy utilization High performance liquid chromatography Ion exchange Particle size Glyphosate N-nitrosoglyphosate Post-derivatization Nitrogen compounds |
description |
A simple and sensitive HPLC post-derivatization method with colorimetric detection has been developed for the determination of N-nitroso glyphosate in samples of technical glyphosate. Separation of the analyte was accomplished using an anionic exchange resin (2.50 mm × 4.00 mm i.d., 15 μm particle size, functional group: quaternary ammonium salt) with Na2SO4 0.0075 M (pH 11.5) (flow rate: 1.0 mL min-1) as mobile phase. After separation, the eluate was derivatized with a colorimetric reagent containing sulfanilamide 0.3% (w/v), [N-(1-naphtil)ethilendiamine] 0.03% (w/v) and HCl 4.5 M in a thermostatized bath at 95 °C. Detection was performed at 546 nm. All stages of the analytical procedure were optimized taking into account the concept of analytical minimalism: less operation times and costs; lower sample, reagents and energy consumption and minimal waste. The limit of detection (k = 3) calculated for 10 blank replicates was 0.04 mg L-1 (0.8 mg kg-1) in the solid sample which is lower than the maximum tolerable accepted by the Food and Agriculture Organization of the United Nations. © 2007 Elsevier B.V. All rights reserved. |
format |
JOUR |
author |
Kim, M. Stripeikis, J. Iñón, F. Tudino, M. |
author_facet |
Kim, M. Stripeikis, J. Iñón, F. Tudino, M. |
author_sort |
Kim, M. |
title |
A simplified approach to the determination of N-nitroso glyphosate in technical glyphosate using HPLC with post-derivatization and colorimetric detection |
title_short |
A simplified approach to the determination of N-nitroso glyphosate in technical glyphosate using HPLC with post-derivatization and colorimetric detection |
title_full |
A simplified approach to the determination of N-nitroso glyphosate in technical glyphosate using HPLC with post-derivatization and colorimetric detection |
title_fullStr |
A simplified approach to the determination of N-nitroso glyphosate in technical glyphosate using HPLC with post-derivatization and colorimetric detection |
title_full_unstemmed |
A simplified approach to the determination of N-nitroso glyphosate in technical glyphosate using HPLC with post-derivatization and colorimetric detection |
title_sort |
simplified approach to the determination of n-nitroso glyphosate in technical glyphosate using hplc with post-derivatization and colorimetric detection |
url |
http://hdl.handle.net/20.500.12110/paper_00399140_v72_n3_p1054_Kim |
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