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首页> 外文期刊>Analytical chemistry >Contribution to Accurate Spherical Gold Nanoparticle Size Determination by Single-Particle Inductively Coupled Mass Spectrometry: A Comparison with Small-Angle X-ray Scattering
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Contribution to Accurate Spherical Gold Nanoparticle Size Determination by Single-Particle Inductively Coupled Mass Spectrometry: A Comparison with Small-Angle X-ray Scattering

机译:单颗粒电感耦合质谱法测定精确球形金纳米粒子尺寸的贡献:与小角度X射线散射的比较

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摘要

Small-angle X-ray scattering spectroscopy (SAXS) is the method of choice for nanoparticle diameter and concentration determination. On the one hand, it is metrologically traceable for spherical nanoparticle mean diameter determination and does not require any sample preparation or calibration. On the other hand, single-particle inductively coupled mass spectrometry (SPICPMS) is still under development and requires involved process clarification and accuracy improvement. The strategy of this study is the comparison of the two techniques to study comprehensively SPICPMS performance and observe phenomena otherwise hidden. Six spherical gold nanoparticle suspensions distributed over a large size range (30, 50, 60, 80,100, and 150 nm) are studied as calibration points. Potential matrix effects are eliminated by stabilizing nanoparticles with chitosan in HCl. Chitosan encapsulates nanoparticles, stabilizes their dispersion, and protects them from dissolution. Detection counting/analogue threshold and timeout appear as the relevant parameters for transient signals. They show an influence not only on mean signal but also on signal distribution. The detection tuning proposed allows to linearly calibrate the nanoparticle distribution signal to cubed diameter over the entire range studied with no sensitivity diminution. Comparing the three classical transport efficiency methods, size transport efficiency is shown as the most accurate. The new procedure is validated analyzing three gold nanoparticle suspensions (135, 40, and 50 nm). The results are consistent with SAXS measurements.
机译:小角度X射线散射光谱(SAX)是纳米颗粒直径和浓度测定的选择方法。一方面,对于球形纳米颗粒平均直径测定并且不需要任何样品制备或校准。另一方面,单粒子电感耦合质谱(SPICPMS)仍在开发中,需要涉及过程澄清和准确性改进。该研究的策略是比较两种技术,以全面研究SpiCPMS性能和观察到其他隐藏的现象。分布在大尺寸范围(30,50,60,80,100和150nm)上的六个球形金纳米粒子悬浮液作为校准点。通过在HCl中用壳聚糖稳定纳米颗粒消除潜在的基质效应。壳聚糖包封纳米颗粒,稳定它们的分散体,并保护它们免受溶解。检测计数/模拟阈值和超时显示为瞬态信号的相关参数。它们不仅在均值信号上表现出影响,而且表明了信号分布。所提出的检测调整允许线性地校准纳米颗粒分布信号在没有灵敏度减少的整个范围内以立方体直径。比较三种经典传输效率方法,尺寸传输效率显示为最准确。验证新程序分析三个金纳米粒子悬浮液(135,40和50nm)。结果与萨克斯测量一致。

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  • 来源
    《Analytical chemistry》 |2018年第16期|共9页
  • 作者单位

    Univ Paris Saclay CNRS CEA Nimbe F-91191 Gif Sur Yvette France;

    Univ Paris Saclay CNRS CEA Nimbe F-91191 Gif Sur Yvette France;

    Univ Paris Saclay CNRS CEA Nimbe F-91191 Gif Sur Yvette France;

    Univ Paris Saclay CEA Den Serv Etud Analyt &

    React Surfaces F-91191 Gif Sur Yvette France;

    Univ Paris Saclay CNRS CEA Nimbe F-91191 Gif Sur Yvette France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

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