成核
剪切流
溶解度
聚电解质
化学物理
Crystal(编程语言)
分子
溶剂
胶体
降水
剪切(地质)
剪切速率
材料科学
化学
粒径
化学工程
结晶学
热力学
有机化学
复合材料
粘度
物理化学
物理
聚合物
工程类
气象学
计算机科学
程序设计语言
作者
Jian‐Ke Sun,Yaroslav I. Sobolev,Weiyi Zhang,Qiang Zhuang,Bartosz A. Grzybowski
出处
期刊:Nature
[Springer Nature]
日期:2020-03-04
卷期号:579 (7797): 73-79
被引量:86
标识
DOI:10.1038/s41586-020-2042-1
摘要
The ability to grow properly sized and good quality crystals is one of the cornerstones of single-crystal diffraction, is advantageous in many industrial-scale chemical processes1-3, and is important for obtaining institutional approvals of new drugs for which high-quality crystallographic data are required4-7. Typically, single crystals suitable for such processes and analyses are grown for hours to days during which any mechanical disturbances-believed to be detrimental to the process-are carefully avoided. In particular, stirring and shear flows are known to cause secondary nucleation, which decreases the final size of the crystals (though shear can also increase their quantity8-14). Here we demonstrate that in the presence of polymers (preferably, polyionic liquids), crystals of various types grow in common solvents, at constant temperature, much bigger and much faster when stirred, rather than kept still. This conclusion is based on the study of approximately 20 diverse organic molecules, inorganic salts, metal-organic complexes, and even some proteins. On typical timescales of a few to tens of minutes, these molecules grow into regularly faceted crystals that are always larger (with longest linear dimension about 16 times larger) than those obtained in control experiments of the same duration but without stirring or without polymers. We attribute this enhancement to two synergistic effects. First, under shear, the polymers and their aggregates disentangle, compete for solvent molecules and thus effectively 'salt out' (that is, induce precipitation by decreasing solubility of) the crystallizing species. Second, the local shear rate is dependent on particle size, ultimately promoting the growth of larger crystals (but not via surface-energy effects as in classical Ostwald ripening). This closed-system, constant-temperature crystallization driven by shear could be a valuable addition to the repertoire of crystal growth techniques, enabling accelerated growth of crystals required by the materials and pharmaceutical industries.
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