首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Development, validation and application of a method based on DI-SPME and GC-MS for determination of pesticides of different chemical groups in surface and groundwater samples
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Development, validation and application of a method based on DI-SPME and GC-MS for determination of pesticides of different chemical groups in surface and groundwater samples

机译:基于DI-SPME和GC-MS的地表和地下水样品中不同化学类别农药测定方法的开发,验证和应用

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摘要

A simple and rapid method based on solid-phase micro extraction (SPME) technique followed by gas chromatography-mass spectrometry with selected ion monitoring (GC-MS, SIM) was developed by the simultaneous determination of 16 pesticides of seven different chemical groups [Six organophosphorus (trichlorfon, diazinon, methyl parathion, malathion, fenthion and ethyon), three pyrethroids (bifenhin, permethrin, cypermethrin), two imidazoles (imazalil and prochloraz), two strobilurins (azoxystrobin and pyraclostrobin), one carbamate (carbofuran), one tetrazine (clofentezine), and one triazole (difenoconazole)] in water. The pesticides extraction was done with direct immersion mode (DI-SPME) of the polyacrilate fiber (PA 85μm). The extraction temperature was adjusted to 50°C during 30min, while stirring at 250rpm was applied. After extraction, the fiber was introduced in the GC injector for thermal desorption for 5min. at 280°C. The method was validated using ultra pure water samples fortified with pesticides at different concentration levels and shows good linearity in the concentrations between 0.05 and 250.00ngmL~(-1). The LOD and LOQ ranged, from 0.02 to 0.30ngmL~(-1) and 0.05 to 1.00ngmL~(-1), respectively. Intra-day and inter-day precisions were determined in two concentration levels (5.00 and 50.00ngmL~(-1)). Intra-day relative standard deviation (%R.S.D.) ranged between 3.6 and 13.6%, and inter-day (%R.S.D.) ranged between 6.3 and 18.5%. Relative recovery tests were carried out spiking the ultra pure sample with standards in three different concentration levels 0.20, 5.00 and 50.00ngmL~(-1). The recovery at 0.20ngmL~(-1) level varied from 86.4±9.4% to 108.5±10.5%, at 5.00ngmL~(-1) level varied from 77.5±10.8% to 104.6±9.6% and at 50.00ngmL~(-1) level varied from 70.2±4.6% to 98.4±8.5%. The proposed SPME method was applied in twenty-six water samples collected in the "Plat? de Neópolis", State of Sergipe, Brazil. Methyl parathion was detected in five samples with an average concentration of 0.17ngmL~(-1) and bifenthrin, pyraclostrobin and azoxystrobin residues were found in three samples with average concentrations of 2.28, 3.12 and 0.15ngmL~(-1), respectively.
机译:通过同时测定七个不同化学类别的16种农药,开发了一种基于固相微萃取(SPME)技术,然后通过气相色谱-质谱联用选择的离子监测(GC-MS,SIM)的简单快速方法[6]有机磷(敌百虫,二嗪农,甲基对硫磷,马拉硫磷,二硫磷和乙硫磷),三种拟除虫菊酯(联苯菊酯,氯菊酯,氯氰菊酯),两种咪唑类(咪唑和丙草胺),两种嗜球果素(氮杂双氧嘧啶和吡唑氯磺胺),一种氨基甲酸酯(四氨基甲酸酯) (氯苯哌嗪)和一种三唑(地非诺康唑)]放在水中。农药的提取采用聚丙烯酸酯纤维(PA85μm)的直接浸没模式(DI-SPME)进行。在30分钟内将萃取温度调节​​至50℃,同时施加250rpm的搅拌。提取后,将纤维引入GC进样器进行5分钟的热脱附。在280°C下使用不同浓度的农药强化的超纯水样品验证了该方法的有效性,并且在0.05至250.00ngmL〜(-1)的浓度范围内显示出良好的线性。 LOD和LOQ分别为0.02至0.30ngmL〜(-1)和0.05至1.00ngmL〜(-1)。在两个浓度水平(5.00和50.00ngmL〜(-1))中确定日内和日间精度。日内相对标准偏差(%R.S.D。)在3.6和13.6%之间,日间(%R.S.D。)在6.3和18.5%之间。进行了相对回收率测试,以0.20、5.00和50.00ngmL〜(-1)三种不同浓度的标准品加标超纯样品。 0.20ngmL〜(-1)水平的回收率从86.4±9.4%变化到108.5±10.5%,5.00ngmL〜(-1)水平的回收率从77.5±10.8%变化到104.6±9.6%,50.00ngmL〜(- 1)水平从70.2±4.6%到98.4±8.5%不等。拟议的SPME方法应用于在巴西塞尔吉比州“ Plat?deNeópolis”采集的26个水样中。在五个平均浓度为0.17ngmL〜(-1)的样品中检出了甲基对硫磷,在三个平均浓度分别为2.28、3.12和0.15ngmL〜(-1)的样品中发现了联苯菊酯,吡菌酯和嘧菌酯残留。

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