首页> 外文期刊>International journal of environmental analytical chemistry >Combination of ultrasonic-assisted dispersive liquid phase micro-extraction with magnetic dispersive solid-phase extraction for the pre-concentration of trace amounts of atrazine in various water samples
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Combination of ultrasonic-assisted dispersive liquid phase micro-extraction with magnetic dispersive solid-phase extraction for the pre-concentration of trace amounts of atrazine in various water samples

机译:超声波辅助分散液相微 - 萃取与磁性色散固相提取的组合,用于各种水样中痕量阿特拉嗪的预浓度

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Herein, ultrasonic-assisted liquid phase micro-extraction in tandem with dispersive ?-solid-phase extraction was utilised for the determination of atrazine at ?g L-?1 concentration levels. Initially, a liquid phase micro-extraction based on dispersion of organic solvent was used for the rapid extraction of atrazine from aqueous solution followed by the extraction organic solvent effectively collected from the solution by using C-18-magnetic nanoparticles without any requirement to centrifugation step. After the elution of the extracted targets from the magnetic nanoparticles, atrazine concentration was monitored by high-performance liquid chromatography with Ultraviolet detector at ?g L-?1 level. The influencial parameters in the pre-concentration step were as follows: pH of solution, magnetic-based sorbent amount (mg) and 1-octanol volume (?L). Additionally, the selected data for the factors produced by the Box-Behnken design were: pH of sample: 9.0, sorbent amount: 22 mg and the extraction solvent volume: 36 ?L. Relative standard deviations under the optimised conditions by the hybrid mentioned extraction method was determined to be 7% and the method detection limit for atrazine was calculated to be 0.3 ?g L-?1. Limit of quantification was calculated to be 0.8 ?g/L for the studied analyte.
机译:这里,利用分散β-溶相萃取串联的超声辅助液相微萃取用于测定αg1-Δ1浓度水平的尿嘧啶。最初,基于有机溶剂的分散体的液相微萃取用于通过使用C-18-磁性纳米颗粒从溶液中有效地收集的萃取有机溶剂,而不需要离心步骤。从磁性纳米颗粒洗脱萃取的靶后,通过高性能液相色谱法监测阿特拉嗪浓度,用紫外线检测器在ΔG1-β1水平上监测。预浓缩步骤中的流入参数如下:溶液的pH,磁性吸附剂量(Mg)和1-辛醇体积(α1)。此外,由Box-Behnken设计产生的因素的所选数据是:样品的pH:9.0,吸附剂量:22 mg和萃取溶剂体积:36μl。通过杂交提到的提取方法在优化条件下的相对标准偏差被确定为7%,并且亚唑的方法检测限为0.3Ω·Δ1。计算定量限制为所研究的分析物的0.8×g / l。

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