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A Multi-Method Approach for Quantification of Surface Coatings on Commercial Zinc Oxide Nanomaterials

机译:商用氧化锌纳米材料表面涂层定量的多方法方法

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摘要

Surface functionalization is a key factor for determining the performance of nanomaterials in a range of applications and their fate when released to the environment. Nevertheless, it is still relatively rare that surface groups or coatings are quantified using methods that have been carefully optimized and validated with a multi-method approach. We have quantified the surface groups on a set of commercial ZnO nanoparticles modified with three different reagents ((3-aminopropyl)-triethoxysilane, caprylsilane and stearic acid). This study used thermogravimetric analysis (TGA) with Fourier transform infrared spectroscopy (FT-IR) of evolved gases and quantitative solution H nuclear magnetic resonance (NMR) for quantification purposes with C-solid state NMR and X-ray photoelectron spectroscopy to confirm assignments. Unmodified materials from the same suppliers were examined to assess possible impurities and corrections. The results demonstrate that there are significant mass losses from the unmodified samples which are attributed to surface carbonates or residual materials from the synthetic procedure used. The surface modified materials show a characteristic loss of functional group between 300–600 °C as confirmed by analysis of FT-IR spectra and comparison to NMR data obtained after quantitative release/extraction of the functional group from the surface. The agreement between NMR and TGA estimates for surface loading is reasonably good for cases where the functional group accounts for a relatively large fraction of the sample mass (e.g., large groups or high loading). In other cases TGA does not have sufficient sensitivity for quantitative analysis, particularly when contaminants contribute to the TGA mass loss. X-ray photoelectron spectroscopy and solid state NMR for selected samples provide support for the assignment of both the functional groups and some impurities. The level of surface group loading varies significantly with supplier and even for different batches or sizes of nanoparticles from the same supplier. These results highlight the importance of developing reliable methods to detect and quantify surface functional groups and the importance of a multi-method approach.
机译:表面功能化是决定纳米材料在一系列应用中的性能及其释放到环境中时的命运的关键因素。尽管如此,使用经过仔细优化和通过多方法验证的方法对表面基团或涂层进行量化仍然相对罕见。我们已经量化了用三种不同的试剂((3-氨基丙基)-三乙氧基硅烷,辛基硅烷和硬脂酸)改性的一组商业ZnO纳米颗粒的表面基团。这项研究使用逸出气体的热重分析(TGA)和傅立叶变换红外光谱(FT-IR)以及定量溶液H核磁共振(NMR)进行定量分析,并使用C固态NMR和X射线光电子能谱确认分配。检查了来自同一供应商的未改性材料,以评估可能的杂质和纠正措施。结果表明,未经修饰的样品存在明显的质量损失,这归因于所用合成方法中的表面碳酸盐或残留物质。经表面改性的材料显示出在300-600°C之间的官能团的特征损失,这已通过FT-IR光谱分析和与从表面定量释放/提取官能团后获得的NMR数据进行了比较。对于官能团占样品质量相对较大部分(例如大基团或高负载)的情况,NMR和TGA估算值之间的表面负载一致性相当好。在其他情况下,TGA对定量分析没有足够的敏感性,尤其是当污染物导致TGA质量损失时。所选样品的X射线光电子能谱和固态NMR为官能团和一些杂质的分配提供了支持。表面基团负载的水平随供应商而变化很大,甚至对于同一供应商的不同批次或大小的纳米颗粒而言,也是如此。这些结果突出了开发检测和定量表面官能团的可靠方法的重要性以及多方法方法的重要性。

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