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Carbonation of ternary building cementing materials
Affiliation:1. 2;2. Mineral Economics Department, Korea Institute of Geosciences and Mineral Resources, 124 Gwahang-no, Yuseong-gu, Daejeon 305-350, Republic of Korea;1. Concrete and Environment Group, Magnel Laboratory for Concrete Research, Department of Structural Engineering, Ghent University, Technologiepark Zwijnaarde 904, B-9052 Ghent, Belgium;2. Polymer Chemistry & Biomaterials Research Group, Department of Macromolecular and Organic Chemistry, Ghent University, Krijgslaan 281, Building S4-bis, B-9000 Ghent, Belgium;3. Center for Microsystems Technology (CMST), IMEC, and Ghent University, Technologiepark 914A, B-9052 Ghent, Belgium;4. Biomaterials Group, Department of Basic Medical Sciences, Ghent University, De Pintelaan 185, Building B, 4th Fl, B-9000 Ghent, Belgium;1. Geomateriales-Unidad asociada (CSIC-UAM), Universidad Autónoma de Madrid, 28049 Madrid, Spain;2. Institute for the Structure of Matter (IEM-CSIC), 28006 Madrid, Spain;3. Polytechnic University of Cataluña, 08028 Barcelona, Spain;4. Eduardo Torroja Institute (IETcc-CSIC), 28033 Madrid, Spain
Abstract:The carbonation processes of ettringite and calcium aluminate hydrates phases developed by hydration of calcium aluminate cement, fly ash and calcium sulphate ternary mixtures have been studied. The hydrated samples were submitted to 4% of CO2 in a carbonation chamber, and were analysed, previous carbonation and after 14 and 90 days of carbonation time, by infrared spectroscopy and X-ray diffraction; the developed morphology was performed with the 14 days carbonated samples. The results evidenced that ettringite reacts with CO2 after 14 days of exposition time and evolves totally at 90 days; the developed hydrated phases C3AH6 in samples with major CAC content, also reacts with CO2. Due to carbonation, calcium carbonate – mainly vaterite but also aragonite-, depending on the initial formulation, aluminium hydroxide and gypsum were detected.
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