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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >INFLUENCE OF THE SOLID-PHASE EXTRACTION PROCESS ON CALIBRATION AND PERFORMANCE PARAMETERS FOR THE DETERMINATION OF PESTICIDE RESIDUES IN WATER BY GAS CHROMATOGRAPHY
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INFLUENCE OF THE SOLID-PHASE EXTRACTION PROCESS ON CALIBRATION AND PERFORMANCE PARAMETERS FOR THE DETERMINATION OF PESTICIDE RESIDUES IN WATER BY GAS CHROMATOGRAPHY

机译:固相萃取过程对气相色谱法测定水中农药残留的校准和性能参数的影响

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摘要

Twenty-six organophosphorus, organochlorine and other electron-capture detection-sensitive pesticides were extracted from water in a single step using a C-18 solid-phase extraction cartridge, eluted with ethyl acetate and isooctane and determined by gas chromatography with electron-capture and flame photometric detection. The calibration equation for the extraction method was calculated for a twentyfold concentration range, including the EC limit of 0.1 mu g/l. The linearity, precision, sensitivity and detection limit of the method were studied, applying the statistical model of linear regression. A lack of linearity was observed for fenthion, deltamethrin and trifluralin, but the proposed method was suitable for other pesticides studied. The limits of detection range from 20 to 120 ng II applying the calibration graph and from 1 to 40 ng/l based on a signal-to-noise ratio of 3:1.
机译:使用C-18固相萃取小柱从水中一步提取26种有机磷,有机氯和其他电子捕获检测敏感农药,用乙酸乙酯和异辛烷洗脱,并通过电子捕获和气相色谱测定。火焰光度检测。计算了萃取方法的校准方程式,浓度范围为20倍,其中EC限值为0.1μg / l。应用线性回归统计模型,研究了该方法的线性,精密度,灵敏度和检出限。硫磷,溴氰菊酯和三氟拉林缺乏线性,但该方法适用于其他农药研究。应用校准曲线图的检测极限范围为20至120 ng II,基于3:1的信噪比,检测范围为1至40 ng / l。

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