首页> 外文期刊>Analytical chemistry >Simultaneous Determination of Imidazolinone Herbicides from Soil and Natural Waters Using Soil Column Extraction and Off-Line Solid-Phase Extraction Followed by Liquid Chromatography with UV Detection or Liquid Chromatography/ Electrospray Mass Spect
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Simultaneous Determination of Imidazolinone Herbicides from Soil and Natural Waters Using Soil Column Extraction and Off-Line Solid-Phase Extraction Followed by Liquid Chromatography with UV Detection or Liquid Chromatography/ Electrospray Mass Spect

机译:色谱柱和离线固相萃取-液相色谱-紫外检测或液相色谱/电喷雾质谱法同时测定土壤和天然水中的咪唑啉酮类除草剂

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This paper describes the simultaneous quantification of the imidazolinone herbicides (IMIs) imazapyr, m-imaza-methabenz, p-imazamethabenz, m,p-imazamethabenz-methyl, imazethapyr, and imazaquin in two types of sam-pies. (a) Groundwater, lake water, and river water sam-pies were enriched by off-line solid-phase extraction with a Carbograph- 1 cartridge and analyzed by reversed-phase liquid chromatography using a LTV detector (λ = 240 nm). The overall recoveries of IMIs extracted from 1 L of groundwater (fortified with 500-100 ng/L), 0.5 L of lake water (fortified with 500-100 ng/L), and 0.5 L of river water (fortified with 1000-200 ng/L) samples were not lower than 89%. The mean relative standard deviation (RSD) was 5.1% (ranging from 4.1% to 6.8%) in natural water. The detection limits were 30-39 ng/L in groundwater, 43-51 ng/L in lake water, and 55-67 ng/L in river water. The method involves confirmatory analysis by LC/ES-MS in full-scan mode. The dependence of the ion signal intensities on proton concentration in the mobile phase was investigated with a view to optimizing the sensitivity of the ES-MS detector. When LC/ES-MS used, the limit of detection, calculated from extracted-ion current profiles (EICPs), was 4-7 ng/L for groundwater and 9-13 ng/L for river water. (b) Soil sample analysis utilized combined soil column extraction (SCE) and off-line solid phase extraction (SPE) for sample preparation, analyzing with LC/ES-MS under selected ion monitoring (SIM). Several different extractants were evaluated for the purpose of SCE optimization. The system that best optimizes the extractability IMIs from the soil was found to be the mixture CH↓(3)OH/(NH↓(4))↓(2)CO↓(3) (0.1 M, 50:50 v/v). The effect of IMI concentration in the matrix on recovery was evaluated. The total recovery of each IMI from soil at each of the two levels investigated raged from 87% to 95%. Under three ion SIM conditions, the limit of detection (S/N = 3) was 0.1-0.05 ng/g in soil samples.
机译:本文介绍了同时定量两种类型山pies中的咪唑啉酮,间咪唑-美沙芬,对咪唑甲达芬,m,对-咪唑甲达芬-甲基,咪唑乙哌啶和咪唑喹的咪唑啉酮除草剂(IMI)。 (a)用Carbograph-1柱通过离线固相萃取富集地下水,湖水和河水样品,并使用LTV检测器(λ= 240 nm)通过反相液相色谱法进行分析。从1 L地下水(强化为500-100 ng / L),0.5 L湖水(强化为500-100 ng / L)和0.5 L河水(强化为1000-200)中提取的IMI的总回收率ng / L)样品不低于89%。天然水中的平均相对标准偏差(RSD)为5.1%(范围从4.1%到6.8%)。检出限在地下水中为30-39 ng / L,在湖水中为43-51 ng / L,在河水中为55-67 ng / L。该方法涉及在全扫描模式下通过LC / ES-MS进行的确认分析。为了优化ES-MS检测器的灵敏度,研究了流动相中离子信号强度对质子浓度的依赖性。当使用LC / ES-MS时,根据提取离子电流曲线(EICPs)计算得出的检出限为地下水4-7 ng / L,河水9-13 ng / L。 (b)土壤样品分析利用土壤柱萃取法(SCE)和离线固相萃取法(SPE)的组合进行样品制备,并在选定的离子监测(SIM)下使用LC / ES-MS进行分析。为了优化SCE,评估了几种不同的萃取剂。发现最优化从土壤中提取IMI的系统是混合物CH↓(3)OH /(NH↓(4))↓(2)CO↓(3)(0.1 M,50:50 v / v )。评估了基质中IMI浓度对回收率的影响。在两个调查水平中,每个土壤中IMI的总回收率从87%上升到95%。在三种离子SIM条件下,土壤样品的检出限(S / N = 3)为0.1-0.05 ng / g。

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