Abdul Wahab, Trinh Thao My Nguyen, Dylan Singh, Erika La Plante
{"title":"水泥基硅酸镁水合物在空气平衡水中的溶解动力学","authors":"Abdul Wahab, Trinh Thao My Nguyen, Dylan Singh, Erika La Plante","doi":"10.1111/jace.20102","DOIUrl":null,"url":null,"abstract":"<p>Magnesium silicate hydrate (M-S-H) represents a promising alternative to traditional cement, particularly for low-pH construction applications such as nuclear waste encapsulation and carbon dioxide injection. The durability of construction materials, a critical aspect of their suitability for various purposes, is primarily governed by the kinetics of dissolution of the binder phase under service conditions. In this study, we employed in situ atomic force microscopy to assess the dissolution rates of M-S-H in water equilibrated with air. Quantitative analysis based on changes in volume and height revealed dissolution rates ranging from 0.18 to 3.09 × 10<sup>−12</sup> mol/cm<sup>2</sup>/s depending on the precipitate Mg/Si ratio and morphology. This rate surpasses its crystalline analogs, talc (Mg<sub>3</sub>Si<sub>4</sub>O<sub>10</sub>(OH)<sub>2</sub>) and serpentine (Mg<sub>3</sub>(Si<sub>2</sub>O<sub>5</sub>)(OH)<sub>4</sub>), by about three to five orders of magnitude. Interestingly, oriented M-S-H dissolved faster than non-oriented M-S-H. Spatially resolved assessments of dissolution rates facilitated a direct correlation between rates and morphology, showing that edges and smaller crystallites dissolve at a faster pace compared to facets and larger crystallites. The outcomes of this study provide insights into the mechanisms governing the dissolution of M-S-H and the factors dictating its durability. These findings hold implications for the strategic design and optimization of M-S-H for various applications.</p>","PeriodicalId":200,"journal":{"name":"Journal of the American Ceramic Society","volume":"107 12","pages":"8547-8555"},"PeriodicalIF":3.5000,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dissolution kinetics of cementitious magnesium silicate hydrate in air-equilibrated water\",\"authors\":\"Abdul Wahab, Trinh Thao My Nguyen, Dylan Singh, Erika La Plante\",\"doi\":\"10.1111/jace.20102\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Magnesium silicate hydrate (M-S-H) represents a promising alternative to traditional cement, particularly for low-pH construction applications such as nuclear waste encapsulation and carbon dioxide injection. The durability of construction materials, a critical aspect of their suitability for various purposes, is primarily governed by the kinetics of dissolution of the binder phase under service conditions. In this study, we employed in situ atomic force microscopy to assess the dissolution rates of M-S-H in water equilibrated with air. Quantitative analysis based on changes in volume and height revealed dissolution rates ranging from 0.18 to 3.09 × 10<sup>−12</sup> mol/cm<sup>2</sup>/s depending on the precipitate Mg/Si ratio and morphology. This rate surpasses its crystalline analogs, talc (Mg<sub>3</sub>Si<sub>4</sub>O<sub>10</sub>(OH)<sub>2</sub>) and serpentine (Mg<sub>3</sub>(Si<sub>2</sub>O<sub>5</sub>)(OH)<sub>4</sub>), by about three to five orders of magnitude. Interestingly, oriented M-S-H dissolved faster than non-oriented M-S-H. Spatially resolved assessments of dissolution rates facilitated a direct correlation between rates and morphology, showing that edges and smaller crystallites dissolve at a faster pace compared to facets and larger crystallites. The outcomes of this study provide insights into the mechanisms governing the dissolution of M-S-H and the factors dictating its durability. These findings hold implications for the strategic design and optimization of M-S-H for various applications.</p>\",\"PeriodicalId\":200,\"journal\":{\"name\":\"Journal of the American Ceramic Society\",\"volume\":\"107 12\",\"pages\":\"8547-8555\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2024-08-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the American Ceramic Society\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/jace.20102\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, CERAMICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Ceramic Society","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jace.20102","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, CERAMICS","Score":null,"Total":0}
Dissolution kinetics of cementitious magnesium silicate hydrate in air-equilibrated water
Magnesium silicate hydrate (M-S-H) represents a promising alternative to traditional cement, particularly for low-pH construction applications such as nuclear waste encapsulation and carbon dioxide injection. The durability of construction materials, a critical aspect of their suitability for various purposes, is primarily governed by the kinetics of dissolution of the binder phase under service conditions. In this study, we employed in situ atomic force microscopy to assess the dissolution rates of M-S-H in water equilibrated with air. Quantitative analysis based on changes in volume and height revealed dissolution rates ranging from 0.18 to 3.09 × 10−12 mol/cm2/s depending on the precipitate Mg/Si ratio and morphology. This rate surpasses its crystalline analogs, talc (Mg3Si4O10(OH)2) and serpentine (Mg3(Si2O5)(OH)4), by about three to five orders of magnitude. Interestingly, oriented M-S-H dissolved faster than non-oriented M-S-H. Spatially resolved assessments of dissolution rates facilitated a direct correlation between rates and morphology, showing that edges and smaller crystallites dissolve at a faster pace compared to facets and larger crystallites. The outcomes of this study provide insights into the mechanisms governing the dissolution of M-S-H and the factors dictating its durability. These findings hold implications for the strategic design and optimization of M-S-H for various applications.
期刊介绍:
The Journal of the American Ceramic Society contains records of original research that provide insight into or describe the science of ceramic and glass materials and composites based on ceramics and glasses. These papers include reports on discovery, characterization, and analysis of new inorganic, non-metallic materials; synthesis methods; phase relationships; processing approaches; microstructure-property relationships; and functionalities. Of great interest are works that support understanding founded on fundamental principles using experimental, theoretical, or computational methods or combinations of those approaches. All the published papers must be of enduring value and relevant to the science of ceramics and glasses or composites based on those materials.
Papers on fundamental ceramic and glass science are welcome including those in the following areas:
Enabling materials for grand challenges[...]
Materials design, selection, synthesis and processing methods[...]
Characterization of compositions, structures, defects, and properties along with new methods [...]
Mechanisms, Theory, Modeling, and Simulation[...]
JACerS accepts submissions of full-length Articles reporting original research, in-depth Feature Articles, Reviews of the state-of-the-art with compelling analysis, and Rapid Communications which are short papers with sufficient novelty or impact to justify swift publication.