首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >DETERMINATION OF TEN CARBAMATE PESTICIDES IN AQUATIC AND SEDIMENT SAMPLES BY LIQUID CHROMATOGRAPHY-IONSPRAY AND THERMOSPRAY MASS SPECTROMETRY
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DETERMINATION OF TEN CARBAMATE PESTICIDES IN AQUATIC AND SEDIMENT SAMPLES BY LIQUID CHROMATOGRAPHY-IONSPRAY AND THERMOSPRAY MASS SPECTROMETRY

机译:液相色谱-离子色谱-热色谱质谱法测定水产品和沉积物中的十种氨基甲酸酯类农药

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Ten carbamate pesticides which exhibit large differences in polarity were determined simultaneously in various environmental samples, using both column liquid chromatography (LC)-thermospray (TSP) mass spectrometry (MS) and LC-ionspray (ISP) MS. For sample clean-up, column chromatography with three stationary phases, neutral aluminium oxide, Florisil and aminopropyl-bonded modified siIica, were tested. The aminopropyl stationary phase showed the best results, with acetone-dichloromethane (25:75) as eluent; analyte recoveries were 76-100% for all compounds with a relative standard deviation of 2-8%. In the ISP mass spectra of eight of the ten carbamates, the sodium adduct ion, [M + Na](+), was the base peak, while the protonated molecule, [M + H](+), was the most abundant ion with carbendazim and aminocarb. An eluent flow-rate between 100 and 300 mu l/min was found to be optimum, with optimized nebulizer and drying gas how-rates of 350 and 15 l/h, respectively. A capillary voltage of 3.5 kV resulted in the largest total ion current. The optimum extraction voltage with regard to analyte detectability and confirmation purposes was between 15 and 35 V. The detection limits obtained with the LC-ISP-MS system were typically in the 10-60 pg range (10 mu l of 10 mu g/l standard solutions), which is 10-150-fold better than obtained with LC-TSP-MS (selected-ion monitoring mode used in both instances). Large-volume injections of tap water spiked with selected carbamates at a level of 0.1 mu g/l illustrated the potential of LC-ISP-MS with respect to analyte detectability. Furthermore, carbofuran was identified at a concentration level of ca. 5 mu g/l in water samples from the Ebro delta. LC-TSP-MS of oxamyl and methomyl in a sediment sample containing a high percentage of organic matter was adversely affected by the presence of co-extractives. This problem did not occur with LC-ISP-MS.
机译:使用柱液相色谱(LC)-热喷雾(TSP)质谱(MS)和LC-离子喷雾(ISP)MS同时测定了各种环境样品中10种极性差异较大的氨基甲酸酯农药。为了纯化样品,测试了具有三个固定相的柱色谱,即中性氧化铝,Florisil和氨基丙基键合的改性硅胶。氨基丙基固定相的洗脱效果最好,以丙酮-二氯甲烷(25:75)为洗脱剂。所有化合物的分析物回收率均为76-100%,相对标准偏差为2-8%。在十个氨基甲酸酯中的八个的ISP质谱图中,钠加合物离子[M + Na](+)是基峰,而质子化的分子[M + H](+)是最丰富的离子与多菌灵和氨基碳水化合物。发现洗脱液流速在100和300μl/ min之间是最佳的,优化的雾化器和干燥气流速分别为350和15 l / h。 3.5 kV的毛细管电压产生最大的总离子电流。就分析物可检测性和确认目的而言,最佳提取电压为15至35V。使用LC-ISP-MS系统获得的检测限通常在10-60 pg范围内(10μl为10μg/ l)标准解决方案),比LC-TSP-MS(两种情况下均使用选择离子监测模式)获得的结果高10-150倍。自来水大量注入所选氨基甲酸酯含量为0.1μg / l的进样水说明了LC-ISP-MS在分析物可检测性方面的潜力。此外,确定了呋喃丹的浓度水平为。埃布罗三角洲的水样中的浓度为5微克/升共萃取物的存在会对含有高百分比有机物的沉积物样品中的草酰和甲酰的LC-TSP-MS产生不利影响。 LC-ISP-MS不会发生此问题。

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