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dc.contributor.authorAntonio C Lasaga
dc.contributor.authorCarlo Pantano
dc.contributor.authorWilliam B White
dc.contributor.authorPROF. MWAKIO TOLE
dc.date.accessioned2012-10-29T15:58:02Z
dc.date.available2012-10-29T15:58:02Z
dc.date.issued1986
dc.identifier.citationdoi.org/10.1016/0016-7037(86)90191-2en_US
dc.identifier.urihttp://hdl.handle.net/123456789/392
dc.descriptionThe original publication is available at http://www.sciencedirect.com/science/article/pii/0016703786901912en_US
dc.description.abstractNepheline shows first order, congruent dissolution rates, followed by a lowering of the rates due to precipitation of new phases from solution, initially aluminium hydroxides, and later, as the activity of silica in solution increases, amorphous aluminosilicates. The reaction rates obey the law (Tole and Lasaga, 1981; tole, 1982, 1984, 1985): Rimeas = Ridias − ∑jRiprec where Rimeas, is the measured rate of input of ton i into solution during dissolution of nepheline, Ridias is the true rate of nephelinedissolution, and ∑jRiprec is the rate of removal of ion i from solution, either by precipitation or adsorption, summed over all the precipitated phases, j, that incorporate the ion, i. This law predicts that the concentration of ion, i, in solution should increase asymptotically to a steady state value, Cfinnal, determined by the ratio of the rate of input of i into solution by nephelinedissolution and the rate of its removal from solution by precipitation or adsorption, such that, for a first order precipitation reaction, View the MathML source where A is the surface area of nepheline, k+ is the dissolution rate constant, A' is the surface area over which precipitation or adsorption takes place, k−. is the precipitation or adsorption rate constant, and Cieq, is the equilibrium concentration for ion i in contact with the precipitated phase. At low pH, rates of dissolution (Ridiss) obey the law: Ridiss = k+(αH+)1.0, while at high pH, the rate law is Ridiss = k+(αH+)−0.2. Nephelinedissolution rates (Ridiss) exhibit a minimum in the pH range 5–7. Initial rates of consumption of protons indicate that in the acid pH region, a positively charged complex is formed on the nepheline surface by adsorption of protrons. It is postulated that it is the rate of breakdown of the surface complex so formed which determines the rate of dissolution of nepheline. Activation energies for the dissolution of nepheline are in the range 53–77 kJ/mole. Addition of 3 m NaCl to the aqueous solution at pH 5 and 60°C lowers the dissolution rate by an order of magnitude. The most stable conditions (i.e. conditions under which a mineral is least reactive) for nepheline are in the pH range 5 ⩽ pH ⩽ 7, and in highly saline aqueous solutions.en_US
dc.description.sponsorshipPwani Universityen_US
dc.language.isoenen_US
dc.publisherELSELVIERen_US
dc.subjectkineticsen_US
dc.subjectdissolutionen_US
dc.subjectnephelineen_US
dc.titleThe kinetics of dissolution of nepheline (NaAlSiO4)en_US
dc.typeArticleen_US


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