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Size characterization and quantification of silver nanoparticles by asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry

机译:非对称流场-流分馏与电感耦合等离子体质谱联用对银纳米颗粒的尺寸表征和定量

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摘要

A method for determining the size of silver nanoparticles and their quantification by asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry (ICP-MS) is proposed and was tested in consumer products. Experimental conditions were studied in detail to avoid aggregation processes or alteration of the original size distributions. Additionally, losses from sorption processes onto the channel membrane were minimized for correct quantification of the nanoparticles. Mobile phase composition, injection/focusing, and fractionation conditions were evaluated in terms of their influence on both separation resolution and recovery. The ionic strength, pH, and the presence of ionic and nonionic surfactants had a strong influence on both separation and recovery of the nanoparticles. In general, better results were obtained under those conditions that favored charge repulsions with the membrane. Recovery values of 83 ± 8% and 93 ± 4% with respect to the content of silver nanoparticles were achieved for the consumer products studied. Silver nanoparticle standards were used for size calibration of the channel. The results were compared with those obtained by photon correlation spectroscopy and images taken by transmission electron microscopy. The quantification of silver nanoparticles was performed by direct injection of ionic silver standard solutions into the ICP-MS system, integration of the corresponding peaks, and interpolation of the fractogram area. A limit of detection of 5.6 μg L-1 silver, which corresponds to a number concentration of 1×1012 L-1 for nanoparticles of 10 nm, was achieved for an injection volume of 20 μL.
机译:提出了一种通过不对称流场-流分馏与电感耦合等离子体质谱法(ICP-MS)来确定银纳米粒子尺寸及其定量方法,并在消费类产品中进行了测试。详细研究了实验条件,以避免聚集过程或原始尺寸分布的改变。另外,为了对纳米颗粒进行正确的定量,将吸附过程在通道膜上的损失最小化。根据流动相组成,进样/聚焦和分馏条件对分离度和回收率的影响,对它们进行了评估。离子强度,pH值以及离子和非离子表面活性剂的存在对纳米颗粒的分离和回收率都有很大影响。通常,在有利于膜带电荷排斥的条件下可获得更好的结果。对于所研究的消费品,相对于银纳米颗粒的含量,回收率达到83±8%和93±4%。银纳米颗粒标准品用于通道的尺寸校准。将结果与通过光子相关光谱法获得的结果和通过透射电子显微镜拍摄的图像进行比较。通过将离子银标准溶液直接注入ICP-MS系统,对相应峰进行积分以及对分数图面积进行插值来对银纳米颗粒进行定量。银的纳米颗粒的检出限为5.6μgL -1 银,对应于1×10 12 L -1 的数浓度进样量为20μL时达到10 nm。

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