结晶
纳米孔
材料科学
降水
石膏
同步加速器
相(物质)
无定形固体
化学物理
晶体生长
化学工程
纳米技术
结晶学
光学
化学
物理
工程类
气象学
有机化学
冶金
作者
Clara Anduix‐Canto,Mark A. Levenstein,Yi‐Yeoun Kim,José R. A. Godinho,Alexander N. Kulak,Carlos González Niño,Philip J. Withers,Jonathan P. Wright,Nikil Kapur,Hugo K. Christenson,Fiona C. Meldrum
标识
DOI:10.1002/adfm.202107312
摘要
Abstract Characterizing the pathways by which crystals form remains a significant challenge, particularly when multiple pathways operate simultaneously. Here, an imaging‐based strategy is introduced that exploits confinement effects to track the evolution of a population of crystals in 3D and to characterize crystallization pathways. Focusing on calcium sulfate formation in aqueous solution at room temperature, precipitation is carried out within nanoporous media, which ensures that the crystals are fixed in position and develop slowly. The evolution of their size, shape, and polymorph can then be tracked in situ using synchrotron X‐ray computed tomography and diffraction computed tomography without isolating and potentially altering the crystals. The study shows that bassanite (CaSO 4 0.5H 2 O) forms via an amorphous precursor phase and that it exhibits long‐term stability in these nanoscale pores. Further, the thermodynamically stable phase gypsum (CaSO 4 2H 2 O) can precipitate by different pathways according to the local physical environment. Insight into crystallization in nanoconfinement is also gained, and the crystals are seen to grow throughout the nanoporous network without causing structural damage. This work therefore offers a novel strategy for studying crystallization pathways and demonstrates the significant impact of confinement on calcium sulfate precipitation, which is relevant to its formation in many real‐world environments.
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