首页> 外文期刊>Journal of Molecular Liquids >A new dendrimer-functionalized magnetic nanosorbent for the efficient adsorption and subsequent trace measurement of Hg (II) ions in wastewater samples
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A new dendrimer-functionalized magnetic nanosorbent for the efficient adsorption and subsequent trace measurement of Hg (II) ions in wastewater samples

机译:一种新的树突式官能化磁纳米吸船,用于有效吸附和随后的废水样品中HG(II)离子的痕量测量

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A new dendrimer-functionalized magnetic nanosorbent for the efficient adsorption and subsequent trace measurement of Hg (II) ions in wastewater samples was successfully synthesized. The synthesis is accomplished via the Michael addition reaction of the amino groups of the silica-coated magnetic nanoparticles (APTES-modified Fe3O4@SiO2) with the double bond of methyl acrylate followed by the amidation of the resulting methyl ester with ethylene diamine. Following that, some donor functional groups were attached to the dendrimer via a specific chemical reaction to offer a further selectivity to the dendrimer-based nanosorbent. Once the synthesis is accomplished, the as-prepared nanosorbent was characterized by several analytical techniques such as FT-IR, SEM, VSM, TGA and EDX. Following that, Hg (II) ions were adsorbed onto the active sites of the sorbent through the complexation with the dentates (-N, -S) of the dispersed sorbent, which seems to be the cornerstone of the adsorption process. In the next step, the ions were desorbed off the sorbent and measured by a cold vapor atomic absorption spectrometer (CV-AAS). The impact of a number of influential variables such as pH, sorbent dosage, adsorption time, elution features were assessed and subsequently optimized. Under the optimal conditions, a relatively wide linearity was obtained for the analyte of interest in the range of 0.08-6.0 mu g/L with the correlation coefficients (R-2) of 0.9922 and the method detection limit (MDL) was determined to be 0.03 mu g/L. Satisfactory relative recoveries of the analyte varied within 90.0-106.7% with the relative standard deviations (RSD%) of 2.1-53%. In addition, a number of experiments with regard to the equilibrium adsorption isotherms of the target ion was performed which well fitted to the Langmuir isotherm model. Finally, the results indicated that the whole method was sensitive, effective and practical for the adsorption and trace measurement of Hg (II) in wastewater samples. (C) 2020 Published by Elsevier B.V.
机译:成功合成了一种新型树枝状高分子功能化磁性纳米吸附剂,用于废水样品中汞(II)离子的高效吸附和后续痕量测量。合成是通过二氧化硅包覆的磁性纳米颗粒(APTES)的氨基的迈克尔加成反应完成的Fe3O4@SiO2)通过丙烯酸甲酯的双键,然后将生成的甲酯与乙二胺酰胺化。随后,通过特定的化学反应将一些供体官能团连接到树状大分子上,以进一步提高树状大分子基纳米吸附剂的选择性。合成完成后,通过FT-IR、SEM、VSM、TGA和EDX等分析技术对所制备的纳米吸附剂进行表征。随后,Hg(II)离子通过与分散吸附剂的齿状物(-N,-S)络合吸附到吸附剂的活性位点上,这似乎是吸附过程的基础。在下一步中,离子从吸附剂上脱附,并通过冷蒸汽原子吸收光谱仪(CV-AAS)进行测量。对pH值、吸附剂用量、吸附时间、洗脱特性等影响因素的影响进行了评估,并对其进行了优化。在最佳条件下,相关分析物在0.08-6.0μg/L范围内获得了相对广泛的线性,相关系数(R-2)为0.9922,方法检测限(MDL)为0.03μg/L。分析物令人满意的相对回收率在90.0-106.7%之间变化,相对标准偏差(RSD%)为2.1-53%。此外,对目标离子的平衡吸附等温线进行了大量实验,这些实验很好地符合朗缪尔等温线模型。结果表明,整个方法对废水样品中Hg(II)的吸附和痕量测定是灵敏、有效和实用的。(C) 2020年爱思唯尔公司出版。

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