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首页> 外文期刊>Revista de Chimie >Simultaneous Determination of Anionic, Amphoteric and Cationic Surfactants Mixtures in Surface Water
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Simultaneous Determination of Anionic, Amphoteric and Cationic Surfactants Mixtures in Surface Water

机译:地表水中阴离子,两性和阳离子表面活性剂混合物的同时测定

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摘要

A simple, reliable and accurate HPLC/CAD method was developed for the determination of anionic (sodium dioctyl sulfosuccinate and sodium 1-dodecane sulfonate), amphoteric (CHAPS (3-[(3-Cholamidopropyl) dimethylammonium]-1-propanesulfonate hydrate)) and cationic (benzethonium chloride) surfactants mixture from surface water samples. The chromatographic analysis was performed on an Acclaim Surfactant Plus (150 x 3.0 mm, 3 μm d.p.) column acquired from Thermo Scientific, kept at 300C. All experiments were performed in gradient elution conditions at a flow-rate of 0.6 mL/min. Mobile phase composition was a mixture of acetonitrile (A) and 0.1 M ammonium acetate solution acidified to pH 5 with acetic acid (B). The limit of detection (LD) were 20 μg/L for anionic surfactants and 30 μg/L for cationic and amphoteric surfactants. The calibration curves were linear between 15 mg/L – 110 mg/L, with R2 values above 0.992 for all surfactants. Solid phase extraction (SPE) using polymeric (Strata X) cartridges has been applied to extract and concentrate the target analytes from the synthetic samples. Surfactants recoveries after SPE procedure were situated between 91.5÷94.6%. Intra-day and inter-day precision (RSD%) were situated between 4.0 ÷ 7.7% and 7.5 ÷ 11.7%, respectively. Limit of quantitation (LQ) was lower than 80 μg/L for anionic surfactants and 90 μg/L for cationic and 100 μg/L for amphoteric surfactants. The new sensitive and selective HPLC/CAD developed method allows simultaneous determination of anionic, amphoteric and cationic surfactants mixture from environmental samples (surface water).
机译:开发了一种简单,可靠和准确的HPLC / CAD方法,用于测定阴离子(二辛基磺酸钠和1-十二烷磺酸钠),两性(3 - [(3-磺酰化)二甲基铵] -1-丙二磺酸盐水合物)))和阳离子(氯化丙酸铵)表面活性剂来自地表水样的混合物。对来自Thermo Scientific的Acclaim Collectant Plus(150×3.0mm,3μm)柱进行色谱分析,保持在300℃。在梯度洗脱条件下以0.6ml / min的流速进行所有实验。流动相组合物是用乙酸(B)酸化至pH5的乙腈(A)和0.1M乙酸铵溶液的混合物。用于阴离子表面活性剂的检测极限(LD)为20μg/ L,用于阳离子和两性表面活性剂的30μg/ L.校准曲线在15mg / L - 110mg / L之间是线性的,所有表面活性剂的R2值高于0.992。使用聚合物(Strata X)盒的固相萃取(SPE)已被应用于从合成样品中提取和浓缩靶分析物。 SPE程序位于91.5‰94.6%之间的表面活性剂回收率。日期和日间精度(RSD%)分别位于4.0‰7.7%和7.5‰11.7%之间。定量限制(LQ)对于阴离子表面活性剂的80μg/ L低于80μg/ l,对于两性表面活性剂的阳离子和100μg/ L的90μg/ L.新的敏感和选择性HPLC / CAD开发方法允许同时测定来自环境样品(表面水)的阴离子,两性和阳离子表面活性剂混合物。

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  • 来源
    《Revista de Chimie》 |2018年第1期|共4页
  • 作者单位

    National Research and Development Institute for Industrial Ecology ECOIND 71-73 Drumul Podu Dambovitei Str. 060652 Bucharest Romania;

    National Research and Development Institute for Industrial Ecology ECOIND 71-73 Drumul Podu Dambovitei Str. 060652 Bucharest Romania;

    National Research and Development Institute for Industrial Ecology ECOIND 71-73 Drumul Podu Dambovitei Str. 060652 Bucharest Romania;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

    HPLC/CAD; SPE; surfactant; surface water;

    机译:HPLC / CAD;SPE;表面活性剂;地表水;

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