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Sampling Methods for Quantification of Solid-state Phases in Powder Samples with Solid-state NMR Spectroscopy

机译:固态NMR光谱法定量粉末样品中固态相的采样方法

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To minimize the variance in the quantification of solid-state phases in powder samples, gently placing polycrystalline samples one next to another directly in a sample holder is better than trying to mix them homogeneously prior to transferring to a sample holder. However, the solid-state cross polarization-magic angle spinning (CP-MAS) nuclear magnetic resonance (NMR) spectroscopy results demonstrated that it is essential in this sampling method to place all the samples in the location of consistent signal sensitivity. The same sampling method may be employed in other spectroscopic quantification techniques of solid-state phases if the method to limit the sample to the location with uniform signal sensitivity in the sample holder is adapted to each technique.
机译:为了最大程度地减少粉末样品中固相定量的差异,将多晶样品一个接一个地轻轻地直接放置在样品架中比将它们均匀混合后再转移到样品架中要好。但是,固态交叉极化-魔角旋转(CP-MAS)核磁共振(NMR)光谱结果表明,在这种采样方法中将所有样本放置在一致的信号灵敏度位置至关重要。如果将样品限制在样品架中信号灵敏度均匀的位置的方法适用于每种技术,则可以在固态相的其他光谱定量技术中采用相同的采样方法。

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