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A simple square wave voltammetric method for the determination of aclonifen herbicide

机译:一种简单的方波伏安法测定阿氯苯胺除草剂

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A cyclic voltammogram of aclonifen was obtained on a glassy carbon electrode at pH 4.0 during the potential scan from 0.00 mV to 1400 mV vs. Ag/AgCI (3 mol L~(-1) NaCI). From repetitive cyclic voltammograms, one anodic peak at +1175 mV and one cathodic peak on the reverse scan at +350 mV were recorded. The sensitive square wave anodic peak at +1220 mV was linearly related to aclonifen concentration ranging from 0.245 to 3.70 μg mL~(-1). The limit of detection (LOD) and the limit of quantification (LOQ) were 0.073 μg mL~(-1) and 0.245 μg mL~(-1) respectively. The percent recoveries of aclonifen calculated from soil and water samples spiked with 1.0 μg mL~(-1) level were 98.80% and 102.40% with the relative standard deviations of 1.82 and 3.61%, respectively. The method was also applied to the herbicide formulation Challenge~R 600 and the average content of 595.3 ± 9.73 g L~(-1) (n = 7, % 95 confidence interval) was consistent with the 600 g L~(-1) aclonifen level quoted by the manufacturer. The considerably high recoveries and low standard deviations provide evidence for the high accuracy and precision of the recommended method.
机译:在相对于Ag / AgCl(3 mol L〜(-1)NaCl)进行的0.00 mV至1400 mV的电势扫描过程中,在pH值为4.0的玻璃碳电极上获得了氯苯芬的循环伏安图。从重复的循环伏安图中,记录到一个在+1175 mV处的阳极峰和一个在+350 mV的反向扫描时的阴极峰。 +1220 mV的灵敏方波阳极峰与氯苯芬浓度在0.245至3.70μgmL〜(-1)之间呈线性关系。检测限(LOD)和定量限(LOQ)分别为0.073μgmL〜(-1)和0.245μgmL〜(-1)。从加标浓度为1.0μgmL〜(-1)的土壤和水样中计算出的氯硝芬的回收率分别为98.80%和102.40%,相对标准偏差分别为1.82和3.61%。该方法也用于除草剂Challenge〜R 600,平均含量为595.3±9.73 g L〜(-1)(n = 7,%95置信区间)与600 g L〜(-1)一致。制造商引用的氯硝芬水平。较高的回收率和较低的标准偏差为推荐方法的高精度和精密度提供了证据。

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