无定形碳酸钙
生物矿化
聚合物
结晶
材料科学
无定形固体
纳米颗粒
化学工程
碳酸钙
生物高聚物
相(物质)
纹理(宇宙学)
纳米棒
纳米技术
结晶学
化学
有机化学
复合材料
人工智能
工程类
图像(数学)
计算机科学
作者
Yifei Xu,Koen C.H. Tijssen,Paul H. H. Bomans,Anat Akiva,Heiner Friedrich,Arno P. M. Kentgens,Nico A. J. M. Sommerdijk
标识
DOI:10.1038/s41467-018-05006-w
摘要
Abstract Many biomineral crystals form complex non-equilibrium shapes, often via transient amorphous precursors. Also in vitro crystals can be grown with non-equilibrium morphologies, such as thin films or nanorods. In many cases this involves charged polymeric additives that form a polymer-induced liquid precursor (PILP). Here, we investigate the CaCO3 based PILP process with a variety of techniques including cryoTEM and NMR. The initial products are 30–50 nm amorphous calcium carbonate (ACC) nanoparticles with ~2 nm nanoparticulate texture. We show the polymers strongly interact with ACC in the early stages, and become excluded during crystallization, with no liquid–liquid phase separation detected during the process. Our results suggest that “PILP” is actually a polymer-driven assembly of ACC clusters, and that its liquid-like behavior at the macroscopic level is due to the small size and surface properties of the assemblies. We propose that a similar biopolymer-stabilized nanogranular phase may be active in biomineralization.
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