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首页> 外文期刊>Reviews in analytical chemistry >Simultaneous determination of dazomet and propanil by partial least squares (PLS-2) and zero-crossing derivative spectrophotometry methods
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Simultaneous determination of dazomet and propanil by partial least squares (PLS-2) and zero-crossing derivative spectrophotometry methods

机译:偏最小二乘(PLS-2)和过零导数分光光度法同时测定达唑麦特和丙烷

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Multicomponent analysis has become one of the most appealing topics for analytical chemists in the last few years. In recent years Partial Least Squares multivariate spectrophotometric calibration (PLS-2) and derivative spectrophotometry have been widely used for the resolution of binary and ternary mixtures and satisfactory results were reported. A simple and fast spectrophotometric method is proposed for the simultaneous determination of Propanil (P), and Dazomet (D) by means the partial least square treatment of the spectrophotometric absorbance data between 200 nm and 320 nm, taken at 5 nm intervals. The method involves the use of 9 standard mixtures of two compounds assayed, considered at three concentration levels and the measurement of the absorbance of samples in 75% ethanol in water solution. A computer program for PLS-2 was written according to the algorithm given by Marten and Naes. For the comparison of the results derivative spectrophotometric procedure (Zero-crossing technique) was used. In this method the D content was determined from the second derivative spectrum by measuring the signal at 284 nm (D-2(284)) (Zero-crossing point for P) and by using appropriate calibration graph. The P content was determined in the same way by measuring the signal at D-2(256.1) (Zero-crossing point for D). Calibration graphs were obtained between 2.0-6.0 mu g.ml(-1) for P and between 3.0-9.0 mu g.ml(-1) for D. When we used first derivative spectrum by measuring the signal at 262.5 nm and 286.9 nm for P and D respectively, we could measure 0.2-1.0 mu g.ml(-1) and 0.5-2.5 mu g.ml(-1) concentration level of D and P. The methods were checked by applying them to the analysis of laboratory prepared mixtures over the concentration ranges 2.0-6.0 for P, and 3.0-9.0 mu g.ml for D.
机译:在过去的几年中,多组分分析已成为分析化学家最有吸引力的主题之一。近年来,偏最小二乘多元分光光度法校准(PLS-2)和导数分光光度法已被广泛用于二元和三元混合物的拆分,并已取得令人满意的结果。提出了一种简单快速的分光光度法,同时对200 nm和320 nm之间的分光光度吸光度数据进行偏最小二乘处理,以5 nm为间隔,同时测定丙胺(P)和达唑美特(D)。该方法涉及使用三种被测化合物的9种标准混合物(在三种浓度水平下考虑),并测量75%乙醇水溶液中样品的吸光度。根据Marten和Naes给出的算法,编写了用于PLS-2的计算机程序。为了比较结果,使用了分光光度法(零交叉技术)。在该方法中,通过测量284 nm处的信号(D-2(284))(P的零交叉点)并使用适当的校准图,从二阶导数光谱中确定D含量。通过测量D-2(256.1)(D的零交叉点)处的信号以相同的方式确定P含量。 P的校正图在2.0-6.0μg.ml(-1)之间,D的校正图在3.0-9.0μg.ml(-1)之间。当我们使用一阶导数光谱时,通过测量262.5 nm和286.9 nm处的信号对于P和D,我们可以分别测量D和P的0.2-1.0μg.ml(-1)和0.5-2.5μg.ml(-1)的浓度水平。实验室配制的混合物中P的浓度范围为2.0-6.0,D的浓度范围为3.0-9.0μg.ml.

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