首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Rapid determination of 95 pesticides in soybean oil using liquid-liquid extraction followed by centrifugation, freezing and dispersive solid phase extraction as cleanup steps and gas chromatography with mass spectrometric detection
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Rapid determination of 95 pesticides in soybean oil using liquid-liquid extraction followed by centrifugation, freezing and dispersive solid phase extraction as cleanup steps and gas chromatography with mass spectrometric detection

机译:使用液-液萃取,离心,冷冻和分散固相萃取作为净化步骤以及气相色谱-质谱检测法快速测定大豆油中的95种农药

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摘要

A multi-residue method using liquid-liquid extraction (LLE) followed by centrifugation, freezing and dispersive solid phase extraction (dispersive SPE) as clean up steps and gas chromatography with mass spectrometric detection has been developed for the determination of trace levels of 95 pesticides in soybean oil. LLE has been optimized to extract these pesticide residues from soybean oil by studying the effect of different partitions between (i) acetonitrile (MeCN) saturated with petroleum ether and a soybean oil solution dissolved in petroleum ether saturated with MeCN, (ii) partition between MeCN and a soybean oil solution dissolved in petroleum ether saturated with MeCN, (iii) partition between MeCN and a soybean oil solution dissolved in petroleum ether, (iv) partition between MeCN saturated with n-hexane and a soybean oil solution dissolved in n-hexane saturated with MeCN, (v) partition between MeCN and a soybean oil solution, (vi) partition between MeCN and a soybean oil solution dissolved in n-hexane and (vii) partition between MeCN and a soybean oil solution dissolved in mixture of acetone and n-hexane (3:2) to the highest recovery yield of pesticides and the lowest co-extract fat residue in the final extract. Experiments were carried out in order to study the efficiency of using centrifugation and freezing steps as well as the used of primary secondary amine (PSA), florisil, graphite carbon black (GCB) and Cl 8 for dispersive SPE on clean up stages to minimize the co-extract fat. The recoveries obtained ranged from 80 to 114% and the relative standard deviation (RSDs) from 2 to 14% for spiking levels of 0.040, 0.080 and 0.160 mg kg(-1). The limits of quantification (LOQs) of almost all compounds were below the maximum residue limits (MRLs) established by the Korean legislations for soybean oil.
机译:已开发出一种多残留方法,该方法采用液-液萃取(LLE),然后进行离心,冷冻和分散固相萃取(分散SPE)作为净化步骤,并采用质谱检测气相色谱法测定痕量的95种农药在大豆油中。通过研究(i)用石油醚饱和的乙腈(MeCN)和溶解在用MeCN饱和的石油醚中的大豆油溶液之间的不同分配的影响,优化了LLE从大豆油中提取这些农药残留,(ii)在MeCN之间的分配以及溶解在用MeCN饱和的石油醚中的大豆油溶液,(iii)在MeCN和溶解在石油醚中的大豆油溶液之间进行分配,(iv)在用正己烷饱和的MeCN和溶解在正己烷中的大豆油之间进行分配用MeCN饱和,(v)在MeCN和大豆油溶液之间分配,(vi)在MeCN和溶于正己烷的大豆油溶液之间分配,以及(vii)在MeCN和溶解在丙​​酮和乙醇混合物中的大豆油溶液分配之间正己烷(3:2)可使农药的回收率最高,最终提取物中的脂肪残留量最低。为了研究使用离心和冷冻步骤的效率以及在清洁阶段使用伯仲胺(PSA),弗洛里西尔,石墨炭黑(GCB)和Cl 8进行分散SPE的效率,以最大程度地减少残留物,进行了实验。共提取脂肪。对于0.040、0.080和0.160 mg kg(-1)的加标浓度,获得的回收率在80%至114%之间,相对标准偏差(RSD)在2%至14%之间。几乎所有化合物的定量限(LOQ)均低于韩国立法规定的大豆油最大残留限(MRL)。

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