Uskoković Vuk
Department of Mechanical and Aerospace Engineering, University of California Irvine, Engineering Gateway 4200, Irvine, CA 92697, USA.
Vib Spectrosc. 2020 May;108. doi: 10.1016/j.vibspec.2020.103045. Epub 2020 Feb 24.
Methods utilizing relatively simple mathematical operations during physical analyses to enable the visualization of otherwise invisible correlations and effects are of particular appeal to researchers and students in pedagogical settings. At the same time, discerning the amorphous phase from its crystalline counterpart in materials is challenging with the use of vibrational spectroscopy and is nowhere as straightforward as in phase composition analytical methods such as X-ray diffraction. A method is demonstrated for the use of first- and second-order differentiation of Fourier transform infrared spectra of calcium phosphates to distinguish their amorphous states from the crystalline ones based on the exact line positioning rather than on comparatively vaguer band broadening and splitting effects. The study utilizes a kinetic approach, focusing on the comparison of spectral features of amorphous precursors annealed in air at different temperatures and aged for different periods of time in an aqueous solution until transforming to one or a mixture of crystalline phases, including hydroxyapatite and α- and β-tricalcium phosphate. One of the findings challenges the concept of the nucleation lag time preceding the crystallization from amorphous precursors as a "dead" period and derives a finite degree of constructive changes occurring at the atomic scale in its course. The differential method for highlighting spectral differences depending on the sample crystallinity allows for monitoring the process of conversion of the amorphous calcium phosphate phase to its crystalline analogue(s). One such method can be of practical significance for synthetic solid state chemists testing for the chemical stability and/or concentration of the reactive amorphous phase in these materials, but also for biologists measuring the maturity of bone and medical researchers evaluating its phase composition and, thus, the state of metabolic and mechanical stability.
在物理分析过程中利用相对简单的数学运算,以使原本不可见的相关性和效应得以可视化的方法,对教学环境中的研究人员和学生具有特别的吸引力。同时,利用振动光谱法从材料的晶体对应物中辨别非晶相具有挑战性,而且不像X射线衍射等相组成分析方法那样直接。本文展示了一种方法,即利用磷酸钙的傅里叶变换红外光谱的一阶和二阶导数,基于精确的谱线定位而非相对模糊的谱带展宽和分裂效应,来区分其非晶态和晶态。该研究采用动力学方法,重点比较了在空气中不同温度下退火并在水溶液中老化不同时间直至转变为一种或多种晶相(包括羟基磷灰石以及α-和β-磷酸三钙)的非晶前驱体的光谱特征。其中一项发现挑战了非晶前驱体结晶之前的成核滞后时间作为“停滞”期的概念,并得出在其过程中原子尺度上发生了有限程度的建设性变化。这种根据样品结晶度突出光谱差异的微分方法,能够监测非晶磷酸钙相转变为其晶体类似物的过程。这样一种方法对于测试这些材料中反应性非晶相的化学稳定性和/或浓度的合成固态化学家具有实际意义,对于测量骨骼成熟度的生物学家以及评估其相组成从而评估代谢和机械稳定性状态的医学研究人员也具有实际意义。