首页> 外文期刊>International journal of environmental analytical chemistry >Simultaneous preconcentration and determination of malachite green and fuchsine dyes in seafood and environmental water samples using nano-alumina-based molecular imprinted polymer solid-phase extraction
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Simultaneous preconcentration and determination of malachite green and fuchsine dyes in seafood and environmental water samples using nano-alumina-based molecular imprinted polymer solid-phase extraction

机译:基于纳米氧化铝的分子印迹聚合物固相萃取同时富集和测定海鲜和环境水样品中的孔雀石绿和品红染料

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摘要

Molecular imprinted polymer for determination of malachite green (MG) and fuchsine basic (FU) dyes by, spectrophotometry has been used, to develop a novel simultaneous extraction and preconcentration method. Molecularly imprinted layer-coated nano-alumina (11/11P@Nano-Al2O3) as adsorbent was prepared by surface molecular imprinting technique, and characterised by FTIR spectroscopy, scanning electron microscopy, energy dispersive X-ray analysis (EDAX) and thermagravimetric analysis (TGA). The method is based on simultaneous extraction of MG and FU dyes from aqueous solution by using molecularly imprinted polymer and measuring the absorbance at 617 and 546 nm for MG and FU, respectively. Parameters which affect the extraction efficiency such as pH, volume of eluent and amount of adsorbent were investigated and optimised. Linear calibration curves were obtained in the range of 2-750 ng mL(-1) for MG and 1-240 ng mL for FU under, optimum conditions. Detection limit based on three times the standard deviation of the blank (3Sb) was 0.655 and 0.245 ng mL(-1) (n = 10) for MG and FU, respectively. The relative standard deviation (RSD) for 100 ng mL(-1) of MG and FU was 2.35 and 3.06% (n = 7), respectively. The method was applied to the simultaneous determination of the dyes in different seafood and environmental water samples.
机译:分子印迹聚合物用于分光光度法测定孔雀石绿(MG)和品红碱性(FU)染料,已开发出一种新型的同时萃取和预浓缩方法。通过表面分子印迹技术制备了分子印迹涂层的纳米氧化铝(11 / 11P @ Nano-Al2O3)作为吸附剂,并通过FTIR光谱,扫描电子显微镜,能量色散X射线分析(EDAX)和热重分析( TGA)。该方法基于通过使用分子印迹聚合物同时从水溶液中提取MG和FU染料并分别测量MG和FU在617和546 nm处的吸光度。研究并优化了影响萃取效率的参数,例如pH,洗脱液体积和吸附剂数量。在最佳条件下,MG的线性校准曲线范围为2-750 ng mL(-1),FU的线性校准曲线范围为1-240 ng mL。 MG和FU基于空白(3Sb)的标准偏差的三倍的检出限分别为0.655和0.245 ng mL(-1)(n = 10)。 MG和FU的100 ng mL(-1)的相对标准偏差(RSD)分别为2.35和3.06%(n = 7)。该方法用于同时测定不同海鲜和环境水样中的染料。

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