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探索非经典结晶途径在推进胶凝材料方面的潜力。

Exploring the Potential of Nonclassical Crystallization Pathways to Advance Cementitious Materials.

作者信息

Ruiz-Agudo Cristina, Cölfen Helmut

机构信息

Physical Chemistry, Department of Chemistry, University of Konstanz, Universitätsstr. 10, 78457 Konstanz, Germany.

出版信息

Chem Rev. 2024 Jun 26;124(12):7538-7618. doi: 10.1021/acs.chemrev.3c00259. Epub 2024 Jun 14.

DOI:10.1021/acs.chemrev.3c00259
PMID:38874016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11212030/
Abstract

Understanding the crystallization of cement-binding phases, from basic units to macroscopic structures, can enhance cement performance, reduce clinker use, and lower CO emissions in the construction sector. This review examines the crystallization pathways of C-S-H (the main phase in PC cement) and other alternative binding phases, particularly as cement formulations evolve toward increasing SCMs and alternative binders as clinker replacements. We adopt a perspective, which recognizes the existence of critical intermediate steps between ions in solution and the final crystalline phases, such as solute ion associates, dense liquid phases, amorphous intermediates, and nanoparticles. These multistep pathways uncover innovative strategies for controlling the crystallization of binding phases through additive use, potentially leading to highly optimized cement matrices. An outstanding example of in cementitious materials is the synthetically produced mesocrystalline C-S-H, renowned for its remarkable flexural strength. This highly ordered microstructure, which intercalates soft matter between inorganic and brittle C-S-H, was obtained by controlling the assembly of individual C-S-H subunits. While large-scale production of cementitious materials by a bottom-up self-assembly method is not yet feasible, the fundamental insights into the crystallization mechanism of cement binding phases presented here provide a foundation for developing advanced cement-based materials.

摘要

了解水泥结合相从基本单元到宏观结构的结晶过程,可以提高水泥性能、减少熟料用量并降低建筑行业的二氧化碳排放量。本综述研究了C-S-H(硅酸盐水泥的主要相)和其他替代结合相的结晶途径,特别是随着水泥配方朝着增加矿渣微粉(SCMs)和替代胶凝材料以替代熟料的方向发展。我们采用一种观点,即认识到溶液中的离子与最终结晶相之间存在关键的中间步骤,如溶质离子缔合物、致密液相、无定形中间体和纳米颗粒。这些多步途径揭示了通过使用添加剂来控制结合相结晶的创新策略,有可能产生高度优化的水泥基体。水泥基材料中一个突出的例子是合成的介晶C-S-H,它以其卓越的抗弯强度而闻名。这种高度有序的微观结构通过控制单个C-S-H亚基的组装,在无机且脆性的C-S-H之间嵌入了软物质。虽然通过自下而上的自组装方法大规模生产水泥基材料目前还不可行,但本文所阐述的对水泥结合相结晶机制的基本见解为开发先进的水泥基材料奠定了基础。

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引用本文的文献

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4D Synchrotron X‑ray Nanoimaging for Early Age Cement Curing: Where Are We and Where Should We Go?用于早期水泥固化的4D同步加速器X射线纳米成像:我们现在所处的位置以及我们应该去往何处?
Acc Mater Res. 2025 May 29;6(7):814-827. doi: 10.1021/accountsmr.5c00018. eCollection 2025 Jul 25.

本文引用的文献

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Multi-step nucleation pathway of C-S-H during cement hydration from atomistic simulations.基于原子模拟的水泥水化过程中C-S-H的多步成核途径
Nat Commun. 2023 Dec 2;14(1):7979. doi: 10.1038/s41467-023-43500-y.
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Atomic-Level and Surface Structure of Calcium Silicate Hydrate Nanofoils.硅酸钙水合物纳米箔的原子级结构和表面结构
J Phys Chem C Nanomater Interfaces. 2023 Sep 8;127(37):18652-18661. doi: 10.1021/acs.jpcc.3c03350. eCollection 2023 Sep 21.
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Armoring of MgO by a Passivation Layer Impedes Direct Air Capture of CO.氧化镁通过钝化层的防腐蚀阻碍了 CO 的直接空气捕捉。
Environ Sci Technol. 2023 Oct 10;57(40):14929-14937. doi: 10.1021/acs.est.3c04690. Epub 2023 Sep 22.
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Unveiling the secret of ancient Maya masons: Biomimetic lime plasters with plant extracts.揭开古玛雅石匠的秘密:用植物提取物制作仿生石灰膏。
Sci Adv. 2023 Apr 21;9(16):eadf6138. doi: 10.1126/sciadv.adf6138. Epub 2023 Apr 19.
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Bottling Liquid-Like Minerals for Advanced Materials Synthesis.为先进材料合成而瓶装液态样矿物。
Adv Mater. 2023 Jun;35(25):e2300702. doi: 10.1002/adma.202300702. Epub 2023 May 1.
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The nucleation of C-S-H via prenucleation clusters.通过预成核簇形成C-S-H的成核过程。
J Chem Phys. 2023 Mar 21;158(11):114309. doi: 10.1063/5.0141255.
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Recent Advances in C-S-H Nucleation Seeding for Improving Cement Performances.用于改善水泥性能的C-S-H成核晶种的最新进展
Materials (Basel). 2023 Feb 9;16(4):1462. doi: 10.3390/ma16041462.
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Hot mixing: Mechanistic insights into the durability of ancient Roman concrete.热拌法:古罗马混凝土耐久性的机理见解。
Sci Adv. 2023 Jan 6;9(1):eadd1602. doi: 10.1126/sciadv.add1602.
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Bioinspired Chiral Template Guided Mineralization for Biophotonic Structural Materials.用于生物光子结构材料的仿生手性模板引导矿化
Adv Mater. 2022 Dec;34(51):e2206509. doi: 10.1002/adma.202206509. Epub 2022 Nov 7.
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Matrix-Directed Mineralization for Bulk Structural Materials.用于块状结构材料的基质导向矿化。
J Am Chem Soc. 2022 Oct 12;144(40):18175-18194. doi: 10.1021/jacs.2c07296. Epub 2022 Sep 26.