Samenvatting
This study attempts to comprehend mechanisms that enhance the photocatalytic properties of autoclaved cementitious pastes. The photocatalytic self-cleaning performance, phase composition, microstructure, optical properties, and silicate chain properties are characterized and analyzed. The results indicate that the silica source and alumina play significant roles in the evolution of phase composition and microstructure, which consequently affects the photocatalytic self-cleaning performance. The impacts of in-situ generated cement hydrates on the photocatalytic performance of cementitious materials are discussed for the first time, as well as the mechanisms governing the different morphologies of C–S–H crystals with the addition of different oxides. For the first time, the role of aluminum incorporation in the C–S–H network and major factors at different stages on the photocatalytic performance of cementitious materials are discussed. Finally, a systematic understanding of the photocatalytic properties of autoclaved cementitious materials is established. These results provide insights into the development of photocatalytic cementitious materials with tailored performances.
Originele taal-2 | Engels |
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Pagina's (van-tot) | 5835-5848 |
Aantal pagina's | 14 |
Tijdschrift | Ceramics International |
Volume | 50 |
Nummer van het tijdschrift | 3, Part B. |
DOI's | |
Status | Gepubliceerd - 1 feb. 2024 |
Financiering
In the nanosilica-enriched system, nanosilica powders dissolve rapidly, resulting in the homogeneous dispersion of Si\u2013O tetrahedrons, along with some Si(OH)4 monomers generated from the dissolution of cement clinkers. Precipitation and crystallization tend to occur preferentially on the surface of TiO2 nanoparticles. However, similar to spontaneous polymerization in solutions, the precipitation of Si(OH)4 monomers on spherical TiO2 particles does not support the oriented growth of C\u2013S\u2013H crystals. Consequently, curved C\u2013S\u2013H crystals, as shown in Fig. 8c, are formed. Moreover, the presence of fewer C\u2013S\u2013H minerals and a greater amount of amorphous C\u2013S\u2013H gel in sample A2 can be attributed to the poor X-ray diffraction signal caused by the unoriented crystallization of C\u2013S\u2013H phases.This research is supported by the National Natural Science Foundation of China (Grant No. 52178246), China Scholarship Council (No. 202006950045), the Department of the Built Environment at Eindhoven University of Technology, and the School of Civil Engineering at Wuhan University. Sincere thanks are given to the Wuhan University and Wuhan University of Technology for the measurement of SEM-EDS, BET, and NMR. This research is supported by the National Natural Science Foundation of China (Grant No. 52178246 ), China Scholarship Council (No. 202006950045 ), the Department of the Built Environment at Eindhoven University of Technology , and the School of Civil Engineering at Wuhan University . Sincere thanks are given to the Wuhan University and Wuhan University of Technology for the measurement of SEM-EDS, BET, and NMR.
Financiers | Financiernummer |
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National Natural Science Foundation of China | 52178246 |
China Scholarship Council | 202006950045 |
Wuhan University | |
Wuhan University of Technology |