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首页> 外文期刊>Environmental Monitoring and Assessment >Magnetic solid phase extraction based on poly( β-cyclodextrin-ester) functionalized silica-coated magnetic nanoparticles (NPs) for simultaneous extraction of the malachite green and crystal violet from aqueous samples
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Magnetic solid phase extraction based on poly( β-cyclodextrin-ester) functionalized silica-coated magnetic nanoparticles (NPs) for simultaneous extraction of the malachite green and crystal violet from aqueous samples

机译:基于聚(β-环糊精 - 酯)官能化二氧化硅涂覆磁性纳米颗粒(NPS)的磁性相萃取,用于同时提取来自水性样品的孔雀石绿和晶体紫萃取

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摘要

In this research, an efficient sorbent based on poly(beta-cyclodextrin-ester)-functionalized silica-coated magnetic nanoparticles (MNPs-CDP) was prepared and used for magnetic solid-phase extraction of the malachite green (MG) and crystal violet (CV) from water samples prior to their determination by high-performance liquid chromatography-ultra violet detection (HPLC-UV). The synthesized nanoparticles were characterized by the field emission-scanning electron microscopy (FE-SEM) and Fourier transform infrared spectroscopy (FT-IR). Of course, the factors, which could influence the extraction efficiency like pH, sorbent amount, salt content, extraction time, desorption time, eluent type, and volume and sample volume, were optimized by response surface methodology. Then, for both of MG and CV, good linearity (0.1-200 mu g L-1, r(2) = 0.99) was achieved under the optimized conditions. The limits of detection (LODs) and the limits of quantification (LOQs), for both of MG and CV, were 0.03 mu g L-1 and 0.1 mu g L-1, respectively. Precision of the method expressed as the relative standard deviations (RSDs) at concentration level of 100 mu g L-1 was 5.6 and 4.2 for MG and CV, respectively. Ultimately, usability of proposed method was investigated by analysis of CV and MG in tap water, fish pond water, and the lake water, and the satisfactory recoveries were obtained in the range of 92-100.5%.
机译:在该研究中,制备基于聚(β-环糊精 - 酯) - 官能化二氧化硅涂覆的磁性纳米颗粒(MNPS-CDP)的有效吸附剂,并用于磁性固相萃取孔雀石绿(Mg)和晶体紫(通过高效液相色谱 - 超紫紫色检测(HPLC-UV)在其测定之前的水样中的CV。通过现场发射扫描电子显微镜(Fe-SEM)和傅里叶变换红外光谱(FT-IR)的特征在于合成的纳米颗粒。当然,通过响应表面方法优化了可能影响pH,吸附剂量,盐含量,提取时间,解吸时间,洗脱液类型和体积和样品体积等提取效率的因素。然后,对于Mg和Cv两者,在优化条件下实现了良好的线性度(0.1-200μg1,r(2)> = 0.99)。 Mg和Cv两者的检测极限(LOD)和定量限制(LOQ)分别为0.03μg-1和0.1μg1-1。表示为浓度为100μg1-1的相对标准偏差(RSD)的方法的精度分别为Mg和Cv的5.6和4.2。最终,通过分析自来水,鱼塘水和湖水中的CV和Mg来研究所提出的方法的可用性,并获得令人满意的回收率在92-100.5%的范围内。

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