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Synthesis and modification of mercapto-submicron scavenger for real-time extraction and preconcentration of As(III)

机译:巯基亚甲基甲基甲基甲基甲基甲硫醇的实时提取和预浓度的合成与改进(III)

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摘要

The gradual increase of arsenic in aquatic layers over the last decades has necessitated the early detection of low levels of arsenic on real time due to its hazardous impact on health. Here, the mercapto-submicron scavenger was synthesized and utilized for solid-phase dispersion extraction technique for real-time extraction and preconcentration of arsenite As(III). Because of particle size, they naturally dispersed without the need for any additional power. The formation of particles and the achievement of the modification of the particles were confirmed by SEM, TEM, size distributions, CHN analysis, FT-IR spectroscopy, micro-Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), zeta potential, energy dispersive X-ray analysis and (EDX) and thermogravimetric analysis (TGA), which confirmed the formation of particles in the size of 253 +/- 34 nm, the chemical implantation of the mercapto groups on the surface was successfully accomplished with a loading of 0.281 mmol g(-1). The particles showed proper dispersion and stability in the aqueous phase before and after being associated with As(III). The chelating process between As(III) and mercapto groups was assessed by XPS which confirmed that the mercapto-submicron scavenger can sequestrate As(III) from water with maximum efficiency. Several factors that could optimize the process were assessed such as the effect of sorbent dose, pH, contact time, sample volumes, eluents, and matrix interference. The As(III) calibration curve showed a positive linear correlation in the range of 0-100 mu g L-1 and coefficient of determination (r(2) = 0.9981). Optimum recovery was obtained with an equilibrium time of 30 min at pH = 8.5. It was found that the release of As(III) from the mercapto-submicron scavenger was eluent dependent and the maximum recovery at the optimum conditions was 98 +/- 3%. The average recovery of As(III) from three different ground water locations was 97.15%.
机译:过去几十年中砷在水生层中的逐步增加需要,由于其对健康的危险性影响,实时地检测了低水平的砷。这里,合成巯基亚微米清除剂并用于固相分散提取技术,用于实时提取和砷酸的前浓度为(III)。由于粒径,它们自然地分散而不需要任何额外的功率。通过SEM,TEM,尺寸分布,CHN分析,FT-IR光谱,微拉曼光谱,X射线光电子能谱(XPS),Zeta电位,能量分散,确认颗粒的形成和颗粒改性的成就。 X射线分析和(EDX)和热重分析(TGA),其证实颗粒的形成为253 +/- 34nm,巯基对表面上的化学注入成功完成,载荷为0.281 mmol g(-1)。颗粒在与(III)相关联之前和之后在水相中显示出适当的分散和稳定性。通过XPS评估AS(III)和巯基之间的螯合过程,该XPS证实巯基亚甲基甲基清除剂可以用最大效率从水中除去(III)。评估可以优化该过程的几个因素,例如吸附剂剂量,pH,接触时间,样品体积,洗脱液和基质干扰的影响。 AS(III)校准曲线显示在0-100μgl-1的范围内的正线性相关性和测定系数(R(2)= 0.9981)。在pH = 8.5下以30分钟的平衡时间获得最佳回收率。结果发现,来自巯基亚微粒清除剂的释放(III)是依赖于洗脱液的,并且最佳条件下的最大恢复为98 +/- 3%。来自三个不同地下水位置的(III)的平均回收率为97.15%。

著录项

  • 来源
    《Analytical methods》 |2018年第2期|共11页
  • 作者单位

    King Abdulaziz City Sci &

    Technol POB 6086 Riyadh 11442 Saudi Arabia;

    Makkah Toxicol Ctr Res Unit Mecca Saudi Arabia;

    Univ Southampton Sch Chem Southampton Hants England;

    Univ Cent Florida Mat Sci &

    Engn MSE Dept Nanosci Technol Ctr NSTC AMPAC Orlando FL 32816 USA;

    Univ Cent Florida Mat Sci &

    Engn MSE Dept Nanosci Technol Ctr NSTC AMPAC Orlando FL 32816 USA;

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  • 正文语种 eng
  • 中图分类 分析化学;
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