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Single particle inductively coupled plasma mass spectrometry with and without flow injection for the characterization of nickel nanoparticles

机译:单颗粒电感耦合等离子体质谱法,无流动注射镍纳米粒子的表征

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This work compares the performance of transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), single particle inductively coupled plasma mass spectrometry (spICPMS) and flow injection (FI) coupled to spICPMS for the characterization of synthetic ferromagnetic Ni nanoparticles (NPs) prepared with and without polyvinylpyrrolidone (PVP) stabilizer. Whereas single NPs measurement by XRD yielded nominal diameters of 13.7 and 16.6 nm with and without PVP respectively, a diameter of 100-130 nm was obtained by TEM and SEM with or without PVP, indicating extensive agglomeration during preparation for microscopy. In contrast, without PVP stabilization, mean and mode sizes of respectively 35 +/- 18 and 21 nm by spICPMS and 33 +/- 15 and 20 nm by FI-spICPMS were obtained for suspensions of Ni NPs using external calibration with Ni standard solutions. With PVP stabilization, the mean and mode sizes respectively decreased to 27 +/- 12 and 18 nm by spICPMS and 25 +/- 10 and 16 nm by FI-spICPMS. Mass balance taking into account the amount of dissolved Ni was verified in all cases. No degradation in performance resulted from using FI-spICPMS instead of spICPMS, even though measurement of NPs mass by FI-spICPMS is done without knowledge of the transport efficiency and the sample uptake rate. This is the first time that spICPMS and FI-spICPMS are demonstrated to be suitable for the characterization of ferromagnetic NPs. (C) 2020 Elsevier B.V. All rights reserved.
机译:该工作比较了透射电子显微镜(TEM),扫描电子显微镜(SEM),X射线衍射(XRD),单粒子电感耦合等离子体质谱(SPICPMS)和流动喷射(FI)的性能,用于表征的SPICPM用含有聚乙烯吡咯烷酮(PVP)稳定剂制备的合成铁磁性Ni纳米颗粒(NPS)。然而,XRD的单个NPS测量分别产生13.7和16.6nm的标称直径,并且分别没有PVP,通过TEM和SEM具有或不具有PVP的直径,表明在制备显微镜期间广泛的聚光。相反,在没有PVP稳定化的情况下,使用外部校准与Ni标准解决方案的外部校准,获得SpICPMS和33 +/-18和21nm的平均和模式尺寸的35 +/-18和21nm,用于使用外部校准,获得Ni NIS的悬浮液。通过PVP稳定化,平均值和模式尺寸分别通过SPICPM和25 +/- 10和16nm降低至27 +/- 12和18nm。考虑到溶解Ni的质量平衡在所有情况下核实。由于使用Fi-SpICPMS而不是SpICPM,因此在没有传输效率和样品摄取率的情况下进行的,因此在使用FI-SPICPMS而不是SPICPMS而不是SPICPMS而不是SPICPM产生的性能下没有降解。这是SpiCPMS和FI-SPICPMS第一次适合于铁磁NPS的表征。 (c)2020 Elsevier B.V.保留所有权利。

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