Optimization of process parameters for determination of trace Hazardous dyes from industrial wastewaters based on nanostructures materials under ultrasound energy

被引:122
作者
Dil, Ebrahim Alipanahpour [1 ]
Ghaedi, Mehrorang [1 ]
Asfaram, Arash [1 ]
Mehrabi, Fatemeh [2 ]
Bazrafshan, Ali Akbar [1 ]
机构
[1] Univ Yasuj, Chem Dept, Yasuj 7591435, Iran
[2] Islamic Azad Univ, Gachsaran Branch, Dept Chem, Gachsaran, Iran
关键词
Ultrasound energy assisted; Multi-responses optimization; Ag-ZnO-NP-AC; Determination of dyes; Derivative spectrophotometry; Experimental design; LIQUID-LIQUID MICROEXTRACTION; SOLID-PHASE EXTRACTION; RESPONSE-SURFACE METHODOLOGY; WATER SAMPLES; ACTIVATED CARBON; METHYL GREEN; ASSISTED EXTRACTION; EXPERIMENTAL-DESIGN; MICROVOLUME SPECTROPHOTOMETRY; DERIVATIVE SPECTROPHOTOMETRY;
D O I
10.1016/j.ultsonch.2017.07.022
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
In this study, ultrasound -assisted dispersive solid phase micro-extraction based on nanosorbent namely silver zinc oxide nanoparticles loaded on activated carbon (Ag-ZnO-NP-AC) combined with derivative spectrophotometry method for the simultaneous pre-concentration and determination of Methyl Green (MG) and Rose Bengal (RB) dyes in water and industrial wastewater. Characterized sorbent by field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), particle-size distribution (PSD), Fourier transform infrared spectroscopy (MR), X-ray powder diffraction (XRD) and Transmission electron microscopy (TEM) analysis with superior adsorption capacity was applied in ultrasound assisted dispersive-solid-phase micro-extraction (UA-DSPME) methodology. pH, sorbent mass, ultrasonication time, and eluent volume influence and contribution on response correspond to simultaneous pre-concentration and determination of MG and RB were optimized by response surface methodology (RSM) and results were compared with the experimental values. Under the optimal conditions (UA-DSPME), the enrichment factors (EFs) were 93.89 and 97.33 for the MG and RB dyes, respectively. The limits of detection were 2.14 and 2.73 ng mL(-1) and the limit of quantification were 7.15 and 9.09 ng mL(-1) for MG and RB, respectively. The analytes can be determined over 10-2000 ng mL(-1) with recoveries between 90.8% to 97.7% and RSDs less than 3.6%. The developed method due to simplicity and rapidity is able successful for repeatable and accurate monitoring of under study analytes from complicated matrices.
引用
收藏
页码:238 / 248
页数:11
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