Crystal transformation and self-assembly theory of microbially induced calcium carbonate precipitation

方解石 碳酸钙 生物矿化 无定形碳酸钙 碳酸盐 化学工程 降水 矿化(土壤科学) 化学 胶结(地质) 矿物学 材料科学 复合材料 有机化学 水泥 物理 工程类 气象学 氮气
作者
Yongqing Chen,Shi‐Qing Wang,Xin-Yang Tong,Xin Kang
出处
期刊:Applied Microbiology and Biotechnology [Springer Nature]
卷期号:106 (9-10): 3555-3569 被引量:25
标识
DOI:10.1007/s00253-022-11938-7
摘要

Microbially induced calcium carbonate precipitation (MICP) is ubiquitous in the earth's lithosphere and brings the inspiration of bionic cementation technology. Over recent years, MICP has been proposed as a potential solution to address many environmental and engineering issues. However, the stability of cemented precipitations generated via MICP technology, especially the characteristics and change mechanism of crystal forms, is still unclear, which substantially hindered the understanding of biomineralization and prohibited the application and upscaling of MICP technology. Here, Sporosarcina pasteurii was selected as a model microbe to induce calcium carbonate mineralization in a series of standard nutrient solutions. The authors studied the process of precipitation from amorphous calcium carbonate to calcite crystal form and revealed the assembly behavior and mechanism of precipitations by FTIR, SEM, TEM and EDS. In the two crystal forms of induced calcium carbonate, the relative position and content of C, O, N, P and Ca elements were only slightly different. The molecular attachment and structural match of organic matrix made the crystals form change. Finally, a self-assembly theory was proposed to MICP, and it provided a solid theoretical basis for the technical specification of MICP technology in engineering application. KEY POINTS: • Organic matrix is intensively involved in MICP by forming functional groups. • Molecular attachment and structural match cause calcite crystal evolution. • A self-assembly theory is proposed for MICP.
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