Hostname: page-component-78c5997874-s2hrs Total loading time: 0 Render date: 2024-11-19T12:22:28.531Z Has data issue: false hasContentIssue false

Kinetics of Alumina Removal from a Calcined Kaolin with Nitric, Sulphuric and Hydrochloric Acids

Published online by Cambridge University Press:  09 July 2018

S. F. Hulbert
Affiliation:
Division of Interdisciplinary Studies, College of Engineering, Clemson University, S. Carolina
D. E. Huff
Affiliation:
Division of Interdisciplinary Studies, College of Engineering, Clemson University, S. Carolina

Abstract

An investigation of the acid-leaching of a calcined kaolin was made to compare the reaction kinetics of hydrochloric, nitric, and sulphuric acids. The acid concentrations used were 5·9 and 8·6 normal. Reaction temperatures used were 95°, 80° and 60° C.

Particular attention was given to finding a reaction equation which would mathematically represent the kinetic data. A nucleation rate equation of the general form, was found to represent these data. Values of m varied from 1·10 to 1·55 depending on the experimental conditions.

Under the conditions employed the rate of alumina leaching is fastest with hydrochloric acid, slower with sulphuric acid, and slowest with nitric acid. The rate controlling steps are proposed from the experimental evidence.

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 1970

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Brindley, G.W., Sharp, J.H. & Patterson, J.H. 0967) Am. Miner. 52, 201.Google Scholar
Carter, R.E. (1961) J. chem. Phys. 34, 2010.CrossRefGoogle Scholar
Christian, J.W. (1965) The Theory of Transformation in Metals and Alloys, p. 471.Google Scholar
Dunwald, H. & Wagner, C. (1934) Z. physik Chem., B24, 53.Google Scholar
Gastuche, M.C., Delmon, B. & Vielvoye, L. (1960) Bull. Soc. chim. Fr., Part 6, 1216.Google Scholar
Giess, E.A. (1963)J. Am. Ceram. Soc. 46, 374.Google Scholar
Ginstling, A.M. & Brounshtein, B.I. (1950) J. appl. Chem. USSR (English transl.) 23, 1327.Google Scholar
Holt, J.B., Cutter, I.B. & Wadsworth, M.E. (1962) J. Am. Ceram. Soc. 45, 133.Google Scholar
Hulbert, S.F. (1969) J. Br. Ceram. Soc. 6, 11.Google Scholar
Hulbert, S.F., Smoak, R.H. & Brosnan, D.A. (1969) Reactivity of Solids (J.W. Mitchell, R.C. Devries, R.W. Roberts & P. Cannon, editors), p. 573, Elsevier Co., New York.Google Scholar
Ibers, J.A. & Davidson, N. (1951) J. Am. chem. Soc. 73, 476.Google Scholar
Jander, W. (]927) Z. anorg, allg. Chem. 163, 1.Google Scholar
Kielland, J. (1937) 3”. Am. chem. Soe. 59, 1675.Google Scholar
Komatsu, W. (1965) Reacticity of Solids (G. M. Schwab, editor) p. 182, Elsevier Co., New York.Google Scholar
Kroger, C. & Ziegler, G. (1953) Glastech. Bet. 26, 346.Google Scholar
Valensi, G. (1936) Comptes Rendues Acad. des ScL 202, 309.Google Scholar
Wagner, C. (1953) Atom Movements, p. 153. Am. Soc. Metals, Cleveland.Google Scholar
Whiteker, R.A. & Davidson, N. (1953) J. Am. chem. Soc. 75, 3081.CrossRefGoogle Scholar
Woods, M.J.M. (1961) Studies of complex ion equilibria: I. Iron (1l) Chloride System 11.Thallium 011) Chloride System. Ph.D thesis (unpublished), University of Wisconsin.Google Scholar
Zhuravlev, V.F., Lesokhin, I.G. & Tempel'man, R.G. (1948) J. appl. Chem. USSR (English Translation) 21, 887.Google Scholar