Zhaoheng Guo , Cheng Liu , Yasong Zhao , Gaofeng Chen , Huixia Wu , Jianming Gao , Hongjian Du
{"title":"纳米二氧化硅对铝酸三钙水合及其与硫酸盐溶液反应的影响","authors":"Zhaoheng Guo , Cheng Liu , Yasong Zhao , Gaofeng Chen , Huixia Wu , Jianming Gao , Hongjian Du","doi":"10.1016/j.cemconres.2024.107706","DOIUrl":null,"url":null,"abstract":"<div><div>Nanosilica (NS) has the potential to enhance the performance of cement-based materials through improvements in pore structure, hydration product content, and the properties of calcium–(aluminum)–silicate–hydrate (C–(A)–S–H) gel, ultimately increasing resistance to sulfate attack. However, the underlying mechanisms of these enhancements remain incompletely understood, particularly with respect to the presence of unhydrated NS particles in blended cementitious materials under sulfate attack. C<sub>3</sub>A (tricalcium aluminate) is one of the main components of cement and a major source of aluminum phases during sulfate attack. This study aims to investigate the effects of NS on the hydration of the C<sub>3</sub>A–gypsum system and the subsequent reaction between the hydration products and sulfates. The investigation involves qualitative and quantitative analyses of the reaction products, and microscopic morphology, as well as tests on ion concentrations, zeta potentials, and sulfate concentrations in the reaction solution. Findings suggest that NS inhibits the formation of ettringite during the C<sub>3</sub>A–gypsum hydration process, but does not exert a notable influence on the final hydration product content. Furthermore, residual NS particles in the C<sub>3</sub>A–NS hydration system further impede the reaction between hydrogarnet and sulfate, thereby reducing ettringite formation. NS also impedes the dissolution of hydrogarnet, resulting in lower concentrations of Ca<sup>2+</sup> and Al<sup>3+</sup> ions and limited consumption of SO<sub>4</sub><sup>2−</sup>. Based on the analysis of the research results, this inhibitory effect is attributed to the adsorption of NS particles onto the hydrogarnet surface, which attracts Ca<sup>2+</sup>, SO<sub>4</sub><sup>2−</sup>, or Ca<img>S ion pair complexes, leading to surface ion overcharging and reduced hydrogarnet dissolution. In addition, NS particles may adsorb onto the surface of ettringite, preventing the adsorption of Ca<sup>2+</sup>, SO<sub>4</sub><sup>2−</sup>, or Ca<img>S ion pair complexes, thereby inhibiting the formation and growth of ettringite.</div></div>","PeriodicalId":266,"journal":{"name":"Cement and Concrete Research","volume":"186 ","pages":"Article 107706"},"PeriodicalIF":10.9000,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Impact of nanosilica on tricalcium aluminate hydration and its reaction with sulfate solutions\",\"authors\":\"Zhaoheng Guo , Cheng Liu , Yasong Zhao , Gaofeng Chen , Huixia Wu , Jianming Gao , Hongjian Du\",\"doi\":\"10.1016/j.cemconres.2024.107706\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Nanosilica (NS) has the potential to enhance the performance of cement-based materials through improvements in pore structure, hydration product content, and the properties of calcium–(aluminum)–silicate–hydrate (C–(A)–S–H) gel, ultimately increasing resistance to sulfate attack. However, the underlying mechanisms of these enhancements remain incompletely understood, particularly with respect to the presence of unhydrated NS particles in blended cementitious materials under sulfate attack. C<sub>3</sub>A (tricalcium aluminate) is one of the main components of cement and a major source of aluminum phases during sulfate attack. This study aims to investigate the effects of NS on the hydration of the C<sub>3</sub>A–gypsum system and the subsequent reaction between the hydration products and sulfates. The investigation involves qualitative and quantitative analyses of the reaction products, and microscopic morphology, as well as tests on ion concentrations, zeta potentials, and sulfate concentrations in the reaction solution. Findings suggest that NS inhibits the formation of ettringite during the C<sub>3</sub>A–gypsum hydration process, but does not exert a notable influence on the final hydration product content. Furthermore, residual NS particles in the C<sub>3</sub>A–NS hydration system further impede the reaction between hydrogarnet and sulfate, thereby reducing ettringite formation. NS also impedes the dissolution of hydrogarnet, resulting in lower concentrations of Ca<sup>2+</sup> and Al<sup>3+</sup> ions and limited consumption of SO<sub>4</sub><sup>2−</sup>. Based on the analysis of the research results, this inhibitory effect is attributed to the adsorption of NS particles onto the hydrogarnet surface, which attracts Ca<sup>2+</sup>, SO<sub>4</sub><sup>2−</sup>, or Ca<img>S ion pair complexes, leading to surface ion overcharging and reduced hydrogarnet dissolution. In addition, NS particles may adsorb onto the surface of ettringite, preventing the adsorption of Ca<sup>2+</sup>, SO<sub>4</sub><sup>2−</sup>, or Ca<img>S ion pair complexes, thereby inhibiting the formation and growth of ettringite.</div></div>\",\"PeriodicalId\":266,\"journal\":{\"name\":\"Cement and Concrete Research\",\"volume\":\"186 \",\"pages\":\"Article 107706\"},\"PeriodicalIF\":10.9000,\"publicationDate\":\"2024-10-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cement and Concrete Research\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0008884624002874\",\"RegionNum\":1,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CONSTRUCTION & BUILDING TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cement and Concrete Research","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0008884624002874","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CONSTRUCTION & BUILDING TECHNOLOGY","Score":null,"Total":0}
Impact of nanosilica on tricalcium aluminate hydration and its reaction with sulfate solutions
Nanosilica (NS) has the potential to enhance the performance of cement-based materials through improvements in pore structure, hydration product content, and the properties of calcium–(aluminum)–silicate–hydrate (C–(A)–S–H) gel, ultimately increasing resistance to sulfate attack. However, the underlying mechanisms of these enhancements remain incompletely understood, particularly with respect to the presence of unhydrated NS particles in blended cementitious materials under sulfate attack. C3A (tricalcium aluminate) is one of the main components of cement and a major source of aluminum phases during sulfate attack. This study aims to investigate the effects of NS on the hydration of the C3A–gypsum system and the subsequent reaction between the hydration products and sulfates. The investigation involves qualitative and quantitative analyses of the reaction products, and microscopic morphology, as well as tests on ion concentrations, zeta potentials, and sulfate concentrations in the reaction solution. Findings suggest that NS inhibits the formation of ettringite during the C3A–gypsum hydration process, but does not exert a notable influence on the final hydration product content. Furthermore, residual NS particles in the C3A–NS hydration system further impede the reaction between hydrogarnet and sulfate, thereby reducing ettringite formation. NS also impedes the dissolution of hydrogarnet, resulting in lower concentrations of Ca2+ and Al3+ ions and limited consumption of SO42−. Based on the analysis of the research results, this inhibitory effect is attributed to the adsorption of NS particles onto the hydrogarnet surface, which attracts Ca2+, SO42−, or CaS ion pair complexes, leading to surface ion overcharging and reduced hydrogarnet dissolution. In addition, NS particles may adsorb onto the surface of ettringite, preventing the adsorption of Ca2+, SO42−, or CaS ion pair complexes, thereby inhibiting the formation and growth of ettringite.
期刊介绍:
Cement and Concrete Research is dedicated to publishing top-notch research on the materials science and engineering of cement, cement composites, mortars, concrete, and related materials incorporating cement or other mineral binders. The journal prioritizes reporting significant findings in research on the properties and performance of cementitious materials. It also covers novel experimental techniques, the latest analytical and modeling methods, examination and diagnosis of actual cement and concrete structures, and the exploration of potential improvements in materials.