TY - JOUR
T1 - Stirring effect on kaolinite dissolution rate
AU - Metz, Volker
AU - Ganor, Jiwchar
N1 - Funding Information:
This research was supported by grant # ES-66-96 from the Israeli Ministry of Energy and Infrastructure and by the Belfer Foundation for Energy and Environmental Research. Volker Metz would like to thank the Minerva Science Foundation for a graduate fellowship. We wish to express our gratitude to A. C. Lasaga, A. Banin, J. Cama, and S. Nir for fruitful discussions and to E. Shani, A. Avital, R. Holzmann, N. Leshem, E. Roueff, G. Ronen, and Y. Shalmi for their technical assistance. We thank the associate editor, Donald Rimstidt, and two anonymous reviewers for their review of the manuscript.
PY - 2001/12/19
Y1 - 2001/12/19
N2 - Experiments were carried out measuring kaolinite dissolution rates using stirred and nonstirred flow-through reactors at pHs 2 to 4 and temperatures of 25°C, 50°C, and 70°C. The results show an increase of kaolinite dissolution rate with increasing stirring speed. The stirring effect is reversible, i.e., as the stirring slows down the dissolution rate decreases. The effect of stirring speed on kaolinite dissolution rate is higher at 25°C than at 50°C and 70°C and at pH 4 than at pHs 2 and 3. It is suggested that fine kaolinite particles are formed as a result of stirring-induced spalling or abrasion of kaolinite. These very fine particles have an increased ratio of reactive surface area to specific surface area, which results in enhancement of kaolinite dissolution rate. A balance between production and dissolution of the fine particles explains both the reversibility and the temperature and pH dependence of the stirring effect. Since the stirring effect on kaolinite dissolution rate varies with temperature and pH, measurement of kinetic parameters such as activation energy may be influenced by stirring. Therefore, standard use of nonagitated reaction vessels for kinetic experiments of mineral dissolution and precipitation is recommended, at least for slow reactions that are surface controlled.
AB - Experiments were carried out measuring kaolinite dissolution rates using stirred and nonstirred flow-through reactors at pHs 2 to 4 and temperatures of 25°C, 50°C, and 70°C. The results show an increase of kaolinite dissolution rate with increasing stirring speed. The stirring effect is reversible, i.e., as the stirring slows down the dissolution rate decreases. The effect of stirring speed on kaolinite dissolution rate is higher at 25°C than at 50°C and 70°C and at pH 4 than at pHs 2 and 3. It is suggested that fine kaolinite particles are formed as a result of stirring-induced spalling or abrasion of kaolinite. These very fine particles have an increased ratio of reactive surface area to specific surface area, which results in enhancement of kaolinite dissolution rate. A balance between production and dissolution of the fine particles explains both the reversibility and the temperature and pH dependence of the stirring effect. Since the stirring effect on kaolinite dissolution rate varies with temperature and pH, measurement of kinetic parameters such as activation energy may be influenced by stirring. Therefore, standard use of nonagitated reaction vessels for kinetic experiments of mineral dissolution and precipitation is recommended, at least for slow reactions that are surface controlled.
UR - http://www.scopus.com/inward/record.url?scp=0035213273&partnerID=8YFLogxK
U2 - 10.1016/S0016-7037(01)00686-X
DO - 10.1016/S0016-7037(01)00686-X
M3 - Article
AN - SCOPUS:0035213273
SN - 0016-7037
VL - 65
SP - 3475
EP - 3490
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
IS - 20
ER -