Lime-calcined clay materials with alkaline activation: Phase development and reaction transition zone
The research aim was to investigate phase development and reaction transition zone of alkaline activated lime-calcined clay materials. Locally available china clay mainly supplied metakaolin (MK) after calcination. MK and calcium hydroxide (CH) were used to supply SiO2and CaO, respectively. The CH t...
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th-cmuir.6653943832-534592018-09-04T09:49:34Z Lime-calcined clay materials with alkaline activation: Phase development and reaction transition zone S. Boonjaeng P. Chindaprasirt K. Pimraksa Earth and Planetary Sciences The research aim was to investigate phase development and reaction transition zone of alkaline activated lime-calcined clay materials. Locally available china clay mainly supplied metakaolin (MK) after calcination. MK and calcium hydroxide (CH) were used to supply SiO2and CaO, respectively. The CH to MK ratio of 0.4 with CaO/SiO2of 1.18 was selected to coincide with the theoretical CaO/SiO2of calcium silicate hydrate in tobermorite group (Ca5Si6O16(OH)2). Phase development was investigated using X-ray diffraction and Fourier transform infrared spectroscopy. Compressive strength and density were also investigated to confirm binding properties of the pozzolanic reaction products. The reaction of mixture was dependent on the NaOH concentration. At low concentration of NaOH (<1M), the pozzolanic reaction was dominant while the zeolitic reaction and geopolymerization became dominant at medium NaOH concentration (>1M) and at high NaOH concentration, respectively. The activations of CH:MK mixtures with 0.01 and 0.1M NaOH promoted semicrystalline calcium silicate hydrate (CSH (I)) and crystalline calcium aluminosilicate hydrate (CASH) formations. The mixture with 0.01M NaOH gave the highest compressive strength of 19.0MPa. With 3 and 5M NaOH activations, sodium aluminosilicate hydrate (NASH) and sodium calcium silicate hydrate (NCSH) compounds were formed instead of CSH (I) gel and crystalline CASH phase. At 10M NaOH, NCSH disappeared and only NASH was formed and resulted in a relatively low compressive strength of 6.7MPa. © 2014 Elsevier B.V. 2018-09-04T09:49:34Z 2018-09-04T09:49:34Z 2014-01-01 Journal 01691317 2-s2.0-84902087431 10.1016/j.clay.2014.05.002 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84902087431&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/53459 |
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Earth and Planetary Sciences S. Boonjaeng P. Chindaprasirt K. Pimraksa Lime-calcined clay materials with alkaline activation: Phase development and reaction transition zone |
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The research aim was to investigate phase development and reaction transition zone of alkaline activated lime-calcined clay materials. Locally available china clay mainly supplied metakaolin (MK) after calcination. MK and calcium hydroxide (CH) were used to supply SiO2and CaO, respectively. The CH to MK ratio of 0.4 with CaO/SiO2of 1.18 was selected to coincide with the theoretical CaO/SiO2of calcium silicate hydrate in tobermorite group (Ca5Si6O16(OH)2). Phase development was investigated using X-ray diffraction and Fourier transform infrared spectroscopy. Compressive strength and density were also investigated to confirm binding properties of the pozzolanic reaction products. The reaction of mixture was dependent on the NaOH concentration. At low concentration of NaOH (<1M), the pozzolanic reaction was dominant while the zeolitic reaction and geopolymerization became dominant at medium NaOH concentration (>1M) and at high NaOH concentration, respectively. The activations of CH:MK mixtures with 0.01 and 0.1M NaOH promoted semicrystalline calcium silicate hydrate (CSH (I)) and crystalline calcium aluminosilicate hydrate (CASH) formations. The mixture with 0.01M NaOH gave the highest compressive strength of 19.0MPa. With 3 and 5M NaOH activations, sodium aluminosilicate hydrate (NASH) and sodium calcium silicate hydrate (NCSH) compounds were formed instead of CSH (I) gel and crystalline CASH phase. At 10M NaOH, NCSH disappeared and only NASH was formed and resulted in a relatively low compressive strength of 6.7MPa. © 2014 Elsevier B.V. |
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author |
S. Boonjaeng P. Chindaprasirt K. Pimraksa |
author_facet |
S. Boonjaeng P. Chindaprasirt K. Pimraksa |
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S. Boonjaeng |
title |
Lime-calcined clay materials with alkaline activation: Phase development and reaction transition zone |
title_short |
Lime-calcined clay materials with alkaline activation: Phase development and reaction transition zone |
title_full |
Lime-calcined clay materials with alkaline activation: Phase development and reaction transition zone |
title_fullStr |
Lime-calcined clay materials with alkaline activation: Phase development and reaction transition zone |
title_full_unstemmed |
Lime-calcined clay materials with alkaline activation: Phase development and reaction transition zone |
title_sort |
lime-calcined clay materials with alkaline activation: phase development and reaction transition zone |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84902087431&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/53459 |
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