Field Dissipation and Storage Stability of Glufosinate Ammonium and Its Metabolites in Soil

A simple analytical method was developed to measure concentrations of glufosinate ammonium and its metabolites, 3-methylphosphinico-propionic acid (MPP) and 2-methylphosphinico-acetic acid (MPA), in field soil samples. To determine the minimum quantification limit, samples were spiked at different l...

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Main Authors: Yun Zhang, Kai Wang, Junxue Wu, Hongyan Zhang
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:International Journal of Analytical Chemistry
Online Access:http://dx.doi.org/10.1155/2014/256091
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spelling doaj-72e990498c914a6786129254602f3ad02020-11-24T20:52:27ZengHindawi LimitedInternational Journal of Analytical Chemistry1687-87601687-87792014-01-01201410.1155/2014/256091256091Field Dissipation and Storage Stability of Glufosinate Ammonium and Its Metabolites in SoilYun Zhang0Kai Wang1Junxue Wu2Hongyan Zhang3College of Science, China Agricultural University, Beijing 100193, ChinaCollege of Science, China Agricultural University, Beijing 100193, ChinaCollege of Science, China Agricultural University, Beijing 100193, ChinaCollege of Science, China Agricultural University, Beijing 100193, ChinaA simple analytical method was developed to measure concentrations of glufosinate ammonium and its metabolites, 3-methylphosphinico-propionic acid (MPP) and 2-methylphosphinico-acetic acid (MPA), in field soil samples. To determine the minimum quantification limit, samples were spiked at different levels (0.1, 0.5, and 1.0 mg/kg). Soil samples were extracted with ammonium hydroxide solution 5% (v/v), concentrated, and reacted with trimethyl orthoacetate (TMOA) in the presence of acetic acid for derivatization. The derivatives were quantified by gas chromatography (GC) using a flame photometric detector (FPD). The linear correlation coefficients of glufosinate ammonium, MPP, and MPA in soil were 0.991, 0.999, and 0.999, respectively. The recoveries of this method for glufosinate ammonium, MPP, and MPA in soil were 77.2–95.5%, 98.3–100.3%, and 99.3–99.6% with relative standard deviations (RSD) of 1.8–4.1%, 0.4–1.4%, and 1.3–2.0%, respectively. Glufosinate ammonium dissipated rapidly in soil to MPA in hours and gradually degraded to MPP. The half-life of glufosinate ammonium degradation in soil was 2.30–2.93 days in an open field. In soil samples stored at −20°C glufosinate ammonium was stable for two months. The results of this study should provide guidance for the safe application of the herbicide glufosinate ammonium to agricultural products and the environment.http://dx.doi.org/10.1155/2014/256091
collection DOAJ
language English
format Article
sources DOAJ
author Yun Zhang
Kai Wang
Junxue Wu
Hongyan Zhang
spellingShingle Yun Zhang
Kai Wang
Junxue Wu
Hongyan Zhang
Field Dissipation and Storage Stability of Glufosinate Ammonium and Its Metabolites in Soil
International Journal of Analytical Chemistry
author_facet Yun Zhang
Kai Wang
Junxue Wu
Hongyan Zhang
author_sort Yun Zhang
title Field Dissipation and Storage Stability of Glufosinate Ammonium and Its Metabolites in Soil
title_short Field Dissipation and Storage Stability of Glufosinate Ammonium and Its Metabolites in Soil
title_full Field Dissipation and Storage Stability of Glufosinate Ammonium and Its Metabolites in Soil
title_fullStr Field Dissipation and Storage Stability of Glufosinate Ammonium and Its Metabolites in Soil
title_full_unstemmed Field Dissipation and Storage Stability of Glufosinate Ammonium and Its Metabolites in Soil
title_sort field dissipation and storage stability of glufosinate ammonium and its metabolites in soil
publisher Hindawi Limited
series International Journal of Analytical Chemistry
issn 1687-8760
1687-8779
publishDate 2014-01-01
description A simple analytical method was developed to measure concentrations of glufosinate ammonium and its metabolites, 3-methylphosphinico-propionic acid (MPP) and 2-methylphosphinico-acetic acid (MPA), in field soil samples. To determine the minimum quantification limit, samples were spiked at different levels (0.1, 0.5, and 1.0 mg/kg). Soil samples were extracted with ammonium hydroxide solution 5% (v/v), concentrated, and reacted with trimethyl orthoacetate (TMOA) in the presence of acetic acid for derivatization. The derivatives were quantified by gas chromatography (GC) using a flame photometric detector (FPD). The linear correlation coefficients of glufosinate ammonium, MPP, and MPA in soil were 0.991, 0.999, and 0.999, respectively. The recoveries of this method for glufosinate ammonium, MPP, and MPA in soil were 77.2–95.5%, 98.3–100.3%, and 99.3–99.6% with relative standard deviations (RSD) of 1.8–4.1%, 0.4–1.4%, and 1.3–2.0%, respectively. Glufosinate ammonium dissipated rapidly in soil to MPA in hours and gradually degraded to MPP. The half-life of glufosinate ammonium degradation in soil was 2.30–2.93 days in an open field. In soil samples stored at −20°C glufosinate ammonium was stable for two months. The results of this study should provide guidance for the safe application of the herbicide glufosinate ammonium to agricultural products and the environment.
url http://dx.doi.org/10.1155/2014/256091
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