Articles & Issues
- Language
- English
- Conflict of Interest
- In relation to this article, we declare that there is no conflict of interest.
- Publication history
-
Received September 26, 2005
Accepted November 4, 2005
- This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright © KIChE. All rights reserved.
All issues
Synthesis of Single Phase Aragonite Precipitated Calcium Carbonate in Ca(OH)2-Na2CO3-NaOH Reaction System
Minerals & Materials Processing Division, Korea Institute of Geoscience & Mineral Resources, Daejeon 305-350, Korea 1Department of Chemical Engineering, Kwangwoon University, Nowon, Seoul 139-701, Korea 2School of Materials Science and Engineering, Seoul National University, Seoul 151-742, Korea
ahnjw@kigam.re.kr
Korean Journal of Chemical Engineering, November 2005, 22(6), 852-856(5), 10.1007/BF02705664
Download PDF
Abstract
The formation behavior of precipitated calcium carbonate polymorphs was investigated in three different supersaturation levels. Because the most easily adjustable and influential variable determining supersaturation is the ion concentration of the major reactants - Ca2+ and CO3_x000D_
2. - the supersaturation can be adjusted by changing the ion concentration of these two ions. At high supersaturation, free energy is necessary for a decrease in nucleation, promoting the formation of a sphere-shaped vaterite, while aragonite and calcite were seen to co-exist at medium supersaturation. At low supersaturation, aragonite was mainly formed by mixing with some calcite. Hence, we considered that lower supersaturation was necessary to obtain a single phase aragonite. Furthermore, we found that the solubility of Ca(OH)2 was decreased with the addition of NaOH by a common ion effect. Thus, it is possible to perform an experiment at a lower Ca2+ concentration. The aragonite was synthesized by adding the Na2CO3 solution to the Ca(OH)2 slurry containing several concentrations of NaOH solution at 75 ℃ and under the addition rate of Na2CO3 at 3 ml/min. The formation yield of calcite decreased when the NaOH concentration was increased. In conclusion, in the case of the reaction of the 2.5M NaOH solution over 210minutes, single-phase aragonite with an aspect ratio of 20 was obtained.
References
Arai T, Yasue T, Gypsum & Lime, 228, 41 (1990)
Dalas E, Kallitsis J, Koutsoukos PG, J. Cryst. Growth, 89, 287 (1988)
Hu ZS, Deng YL, Powder Technol., 140(1-2), 10 (2004)
Kawano J, Shimobayashi N, Kitamura M, Shinoda K, Aikawa N, J. Cryst. Growth, 237-239, 419 (2002)
Kim JH, Ahn JW, Park HS, Park CH, Geosystem Engineering, 7(4), 95 (2004)
Kitamura M, Konno K, J. Cryst. Growth, 236, 323 (2002)
Konno H, Nanri Y, Kitamura M, Powder Technol., 123(1), 33 (2002)
Konno H, Nanri Y, Kitamura M, Powder Technol., 129(1-3), 15 (2003)
van Langerak EPA, Beekmans MMH, Beun JJ, Hamelers HVM, Lettinga G, J. Chem. Technol. Biotechnol., 74(11), 1030 (1999)
Nyvlt J, The Kinetics of Industrial Crystallization, Elsevier, Amsterdam (1985)
Sohnel O, Mullin JW, J. Cryst. Growth, 60, 239 (1982)
Tanaka H, Gypsum & Lime, 227, 229 (1990)
Wang LF, Sondi I, Matijevic E, J. Colloid Interface Sci., 218(2), 545 (1999)
Dalas E, Kallitsis J, Koutsoukos PG, J. Cryst. Growth, 89, 287 (1988)
Hu ZS, Deng YL, Powder Technol., 140(1-2), 10 (2004)
Kawano J, Shimobayashi N, Kitamura M, Shinoda K, Aikawa N, J. Cryst. Growth, 237-239, 419 (2002)
Kim JH, Ahn JW, Park HS, Park CH, Geosystem Engineering, 7(4), 95 (2004)
Kitamura M, Konno K, J. Cryst. Growth, 236, 323 (2002)
Konno H, Nanri Y, Kitamura M, Powder Technol., 123(1), 33 (2002)
Konno H, Nanri Y, Kitamura M, Powder Technol., 129(1-3), 15 (2003)
van Langerak EPA, Beekmans MMH, Beun JJ, Hamelers HVM, Lettinga G, J. Chem. Technol. Biotechnol., 74(11), 1030 (1999)
Nyvlt J, The Kinetics of Industrial Crystallization, Elsevier, Amsterdam (1985)
Sohnel O, Mullin JW, J. Cryst. Growth, 60, 239 (1982)
Tanaka H, Gypsum & Lime, 227, 229 (1990)
Wang LF, Sondi I, Matijevic E, J. Colloid Interface Sci., 218(2), 545 (1999)