J. R. Marius Tuyishime, Edith C. Hammer, Martí Pla-Ferriol, Karina Thånell, Carl Alwmark, Sophie van Velzen, Dimitrios Floudas, Rasa Platakyte, Martin Obst, Hanbang Zou
{"title":"真菌诱导CaCO3沉淀的纳米级表征:对自愈混凝土的影响","authors":"J. R. Marius Tuyishime, Edith C. Hammer, Martí Pla-Ferriol, Karina Thånell, Carl Alwmark, Sophie van Velzen, Dimitrios Floudas, Rasa Platakyte, Martin Obst, Hanbang Zou","doi":"10.1021/acsami.5c07137","DOIUrl":null,"url":null,"abstract":"Cracks in concrete compromise structural integrity by exposing steel reinforcement to corrosion agents, shortening its service life. Fungal-induced calcium carbonate (CaCO<sub>3</sub>) precipitation via urea hydrolysis offers a fast and robust self-healing mechanism to seal the cracks, extending the lifespan while reducing the carbon (C) footprint of concrete infrastructure. However, current studies rely on bulk-scale analytical methods, which lack the spatial resolution and chemical sensitivity to distinguish and map CaCO<sub>3</sub> polymorphs at the nanoscale. This study combined scanning electron microscopy (SEM) and synchrotron-based scanning transmission X-ray microscopy (STXM) with near-edge X-ray absorption fine structure (NEXAFS) spectroscopy to characterize fungal CaCO<sub>3</sub> polymorphs at the nanoscale. CaCO<sub>3</sub> biominerals precipitated by three urease-positive fungi were sectioned into 75–200 nm thin layers. STXM data were collected from at least two spots per section, focusing on Ca (L-edge) and C (K-edge) chemical speciation and elemental quantitative mapping. Calcite, the thermodynamically most stable polymorph, was identified as the predominant mineral phase precipitated by all fungi species, while aragonite and non-CO<sub>3</sub>–Ca species (CaCl<sub>2</sub> or Ca adsorbed onto extracellular polymeric substances (EPS)) occurred as minor components. In fungal species 2, we observed nanoscale heterogeneity in Ca phases across five analyzed spots, three dominated by calcite with minor contributions of other Ca species, while the others showed mixed CaCO<sub>3</sub>/non-CO<sub>3</sub> phases, as confirmed by NEXAFS spectra. These findings suggest that biomineralization in the fungal micro and nanoenvironment is influenced by localized physicochemical and metabolic conditions that shape mineral phases. C NEXAFS spectra further supported the Ca data, showing C-specific spectral features in the calcite-rich regions across all samples. This underscores STXM’s capability to resolve complexities and mechanisms of fungal CaCO<sub>3</sub> formation (e.g., mineral phase composition, fungal organic-mineral interactions, and spatial heterogeneity). Overall, this study provides critical nanoscale insights into fungal CaCO<sub>3</sub> precipitation, thus providing valuable guidance in optimizing fungal systems in self-healing concrete applications.","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"268 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2025-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nanoscale Characterization of Fungal-Induced CaCO3 Precipitation: Implications for Self-Healing Concrete\",\"authors\":\"J. R. Marius Tuyishime, Edith C. 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This study combined scanning electron microscopy (SEM) and synchrotron-based scanning transmission X-ray microscopy (STXM) with near-edge X-ray absorption fine structure (NEXAFS) spectroscopy to characterize fungal CaCO<sub>3</sub> polymorphs at the nanoscale. CaCO<sub>3</sub> biominerals precipitated by three urease-positive fungi were sectioned into 75–200 nm thin layers. STXM data were collected from at least two spots per section, focusing on Ca (L-edge) and C (K-edge) chemical speciation and elemental quantitative mapping. Calcite, the thermodynamically most stable polymorph, was identified as the predominant mineral phase precipitated by all fungi species, while aragonite and non-CO<sub>3</sub>–Ca species (CaCl<sub>2</sub> or Ca adsorbed onto extracellular polymeric substances (EPS)) occurred as minor components. In fungal species 2, we observed nanoscale heterogeneity in Ca phases across five analyzed spots, three dominated by calcite with minor contributions of other Ca species, while the others showed mixed CaCO<sub>3</sub>/non-CO<sub>3</sub> phases, as confirmed by NEXAFS spectra. These findings suggest that biomineralization in the fungal micro and nanoenvironment is influenced by localized physicochemical and metabolic conditions that shape mineral phases. C NEXAFS spectra further supported the Ca data, showing C-specific spectral features in the calcite-rich regions across all samples. This underscores STXM’s capability to resolve complexities and mechanisms of fungal CaCO<sub>3</sub> formation (e.g., mineral phase composition, fungal organic-mineral interactions, and spatial heterogeneity). 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Nanoscale Characterization of Fungal-Induced CaCO3 Precipitation: Implications for Self-Healing Concrete
Cracks in concrete compromise structural integrity by exposing steel reinforcement to corrosion agents, shortening its service life. Fungal-induced calcium carbonate (CaCO3) precipitation via urea hydrolysis offers a fast and robust self-healing mechanism to seal the cracks, extending the lifespan while reducing the carbon (C) footprint of concrete infrastructure. However, current studies rely on bulk-scale analytical methods, which lack the spatial resolution and chemical sensitivity to distinguish and map CaCO3 polymorphs at the nanoscale. This study combined scanning electron microscopy (SEM) and synchrotron-based scanning transmission X-ray microscopy (STXM) with near-edge X-ray absorption fine structure (NEXAFS) spectroscopy to characterize fungal CaCO3 polymorphs at the nanoscale. CaCO3 biominerals precipitated by three urease-positive fungi were sectioned into 75–200 nm thin layers. STXM data were collected from at least two spots per section, focusing on Ca (L-edge) and C (K-edge) chemical speciation and elemental quantitative mapping. Calcite, the thermodynamically most stable polymorph, was identified as the predominant mineral phase precipitated by all fungi species, while aragonite and non-CO3–Ca species (CaCl2 or Ca adsorbed onto extracellular polymeric substances (EPS)) occurred as minor components. In fungal species 2, we observed nanoscale heterogeneity in Ca phases across five analyzed spots, three dominated by calcite with minor contributions of other Ca species, while the others showed mixed CaCO3/non-CO3 phases, as confirmed by NEXAFS spectra. These findings suggest that biomineralization in the fungal micro and nanoenvironment is influenced by localized physicochemical and metabolic conditions that shape mineral phases. C NEXAFS spectra further supported the Ca data, showing C-specific spectral features in the calcite-rich regions across all samples. This underscores STXM’s capability to resolve complexities and mechanisms of fungal CaCO3 formation (e.g., mineral phase composition, fungal organic-mineral interactions, and spatial heterogeneity). Overall, this study provides critical nanoscale insights into fungal CaCO3 precipitation, thus providing valuable guidance in optimizing fungal systems in self-healing concrete applications.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.