Greaves G N, Bras W, Oversluizen M, Clark S M
Department of Physics, University of Wales, Aberystwyth, UK SY23 3BZ.
Faraday Discuss. 2003;122:299-314; discussion 381-93. doi: 10.1039/b202331h.
New Cr X-ray absorption fine structure (XAFS) data have been combined with the results of small angle X-ray scattering (SAXS) and wide angle X-ray scattering (WAXS) experiments to probe in detail the crystallisation mechanism in cordierite (Mg2Al4Si5O18) glass doped with 0.34 mol% Cr2O3. By direct comparison with chromo-aluminate spinels (MgCr2xAl2(1 - x)O4) Cr XAFS is used to determine the composition of the devitrified Cr species. This is identified as MgCr(0.18)Al(1.82)O4, which can be directly related to the Cr content in the starting glass and as a result the total crystalline volume in the fully developed ceramic is predicted to be 4%. In situ WAXS not only reveals the presence of the spinel phase but also a silica-rich stuffed quartz phase. This grows independently of the spinel and is probably nucleated from the glass surface. From our knowledge of the compositions of both crystalline phases we are able to deduce that the SAXS contrast between the surrounding glass and the spinel crystallites is 30 times greater than that between the quartz crystallites and the glass matrix, and therefore dominates the measured scattered intensity and the SAXS invariant that is derived from it. As a consequence we are able to show that the spinel crystalline volume fraction inherent in the SAXS is in close agreement with the 4% value obtained from the Cr XAFS. Furthermore in situ SAXS reveals the gradual development of the spinel particle size and shape during heat treatment. This is conducted in the super-cooled region just above the glass transition temperature, Tg. By employing a two-step annealing process nucleation can be separated from growth and from time-resolved SAXS measurements the alumino-chromate nanocrystals are found to be closely monodispersed. Over a total time course of 600 min they grow from rough crystallites to smooth spherical particles of radius 21 +/- 2 nm, with a final density of (1.2 +/- 0.4) x 10(21) m(-3). As the process of ceramic formation takes place in the viscous melt, growth is indeed found to be limited by diffusion and is complete when all the Cr is exhausted. We use this comprehensive in situ study of crystallisation in cordierite glass to demonstrate the advantages of combining SAXS, WAXS and XAFS for probing the time-resolved chemistry, the microstructure and its development from nucleation sites, that underpins the processing of nanoparticle ceramics.
新的Cr X射线吸收精细结构(XAFS)数据已与小角X射线散射(SAXS)和广角X射线散射(WAXS)实验结果相结合,以详细探究掺杂0.34 mol% Cr₂O₃的堇青石(Mg₂Al₄Si₅O₁₈)玻璃的结晶机制。通过与铬铝酸盐尖晶石(MgCr₂ₓAl₂(₁₋ₓ)O₄)直接比较,利用Cr XAFS确定了析晶Cr物种的组成。其被确定为MgCr(₀.₁₈)Al(₁.₈₂)O₄,这与起始玻璃中的Cr含量直接相关,因此预测完全致密化陶瓷中的总晶相体积为4%。原位WAXS不仅揭示了尖晶石相的存在,还揭示了富含二氧化硅的填充石英相的存在。该相独立于尖晶石生长,可能从玻璃表面成核。根据我们对两种晶相组成了解,能够推断出周围玻璃与尖晶石微晶之间的SAXS对比度比石英微晶与玻璃基体之间的对比度大30倍,因此主导了测量的散射强度以及由此得出的SAXS不变量。结果我们能够表明,SAXS中固有的尖晶石晶相体积分数与从Cr XAFS获得的4%的值非常吻合。此外,原位SAXS揭示了热处理过程中尖晶石颗粒尺寸和形状的逐渐演变。这一过程在略高于玻璃转变温度Tg的过冷区域进行。通过采用两步退火过程,可以将成核与生长分离,并且从时间分辨SAXS测量中发现铝铬酸盐纳米晶体紧密单分散。在总共600分钟的时间过程中,它们从粗糙的微晶生长为半径为21±2 nm的光滑球形颗粒,最终密度为(1.2±0.4)×10²¹ m⁻³。由于陶瓷形成过程在粘性熔体中发生,确实发现生长受扩散限制,并且当所有Cr耗尽时生长完成。我们利用对堇青石玻璃结晶的这一全面原位研究,展示了结合SAXS、WAXS和XAFS在探测时间分辨化学、微观结构及其从成核位点开始的演变方面的优势,这些是纳米颗粒陶瓷加工的基础。