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Optimization and modeling of preconcentration and determination of dyes based on ultrasound assisted-dispersive liquid–liquid microextraction coupled with derivative spectrophotometry

2016; Elsevier BV; Volume: 34; Linguagem: Inglês

10.1016/j.ultsonch.2016.05.013

1873-2828

Ebrahim Alipanahpour Dil, Mehrorang Ghaedi, Arash Asfaram,

Electrochemical Analysis and Applications

Present study is based on describing an ultrasound-assisted dispersive liquid–liquid microextraction coupled with derivative spectrophotometry (UAS-DLLME-UV–vis) as useful technique for selective determination of crystal violet (CV) and azure b (Az-B). The significant factors like pH, extractor volume, disperser value and extraction time contribution and their numerical coefficient in quadratic model were calculated according to central composite design (CCD). According to desirability function (DF) as good criterion the best experimental conditions was adjusted and selected at pH of 7.0, 170 μL of chloroform, 800 μL of ethanol that strongly mixed with the aqueous phase via 4 min sonication. Additionally, under study system was modeled by trained artificial neural networks (ANNs) as fitness function with acceptable error of MSE 2.97 × 10−06 and 1.15 × 10−05 with R2: 0.9999 and 0.9997 for CV and Az-B, respectively. The optimum conditions by using genetic algorithm (GA) method was pH of 6.3, 160 μL of chloroform, 740 μL of ethanol and 4.5 min sonication. Under above specified and optimize conditions, the predicted extraction percentage were 99.80 and 102.20% for CV and Az-B, respectively. The present UAS-DLLME-UV–vis procedure has minimum interference from other substances assign to the matrix, which candidate this method as good alternative to quantify under study dyes content with recoveries in the range of 86–100% for dyes. The detection limits were 2.043 ng mL−1 and 1.72 ng mL−1, and limits of quantitation were 6.81 ng mL−1 and 5.727 ng mL−1 for CV and Az-B, respectively. The proposed methodology was successfully applied for quantification of under study analytes at different media.