Experimental Study of Dissolution Rates of Fluorite in HCl–H2O Solutions

被引:8
作者
Ronghua Zhang
Shumin Hu
Xuetong Zhang
机构
[1] Chinese Academy of Geological Sciences,Open Research Laboratory of Geochemical Kinetics
[2] Institute of Mineral Deposits,undefined
来源
Aquatic Geochemistry | 2006年 / 12卷
关键词
dissolution rates; kinetics; proton adsorption; surface modifications;
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中图分类号
学科分类号
摘要
The experiments of the dissolution kinetics of fluorite were performed in aqueous HCl solutions over the temperature range of 25–100 °C using a flow-through experimental apparatus. With a constant input of aqueous HCl solution through the reactor, output concentrations of the dissolved species Ca, F, Cl vary with flow rate, as well as with the surface compositions. Measured output concentrations of dissolved species and the pH can be used to determine a rate law for fluorite dissolution. Fluorite dissolution rates are found to be pH dependent. Usually, dissolution rates of fluorite decreases with increasing dissolved Ca in the output solution at 25 and 100 °C. Dissolution rate can be expressed as 1a\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$-r=k((a_{\rm H}^{+})^{2}/(a_{\rm Ca}^{2+}))^{\alpha} $$\end{document} where k is the rate constant and α is the order with respect to the hydrogen ion activity vs. the activity of dissolved Ca. The α was obtained from kinetic experiments. For the fluorite sample passed through 18–35 mesh, α =1.198 at 100 °C and k = 10−0.983, while fluorite dissolved in HCl–H2O solution at pH 2.57 of input solution. Adsorption of a proton and Cl−1onto the fluorite surface, surface cation exchange and the formation of the surface complex Ca(F, Cl)2 and/or (H2x, Ca1−x)(F, Cl)2 control dissolution rates. Investigation of the fluorite surface before and after dissolution by using X-ray photoelectron spectroscopy (XPS) indicate that surface modifications affect reaction rates.
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页码:123 / 159
页数:36
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共 121 条
[1]  
Amehein C.(1988)The use surface complexation model t describe the kinetics of ligand-promoted dissolution of anorthite Geochim. Cosmochim. Acta 52 2785-2793
[2]  
Suarez D. L.(1987)Effect of solution composition on the rate and mechanism of gibbsite dissolution in acid solutions Soil. Sci. Soc. Am. J. 51 1131-1136
[3]  
Bloom P. R.(1988)Role of surface speciation in the low-temperature dissolution of minerals Nature 331 431-433
[4]  
Erich M. S.(1991)The role of surface speciation in the dissolution of albite Geochim. Cosmochim. Acta 55 2193-2201
[5]  
Blum A.(1992)Silica surface chemistry at elevated temperatures Geochim. Cosmochim. Acta 56 2914-2946
[6]  
Lasaga A.(1989)Control on silicate dissolution rates in neutral and basic pH solution at 25C Geochim. Cosmochim. Acta 53 2823-2830
[7]  
Blum A. E.(1992)Surface chemistry and silicate dissolution at elevated temperatures Am. J. Sci. 292 639-658
[8]  
Lasaga A. C.(1999)The deviation-from-equilibrium effect on dissolution rate and on apparent variations in activation energy Geochim. Cosmochim Acta 61 2481-2486
[9]  
Brady P. V.(1993)A surface complexation model of the carbonate mineral–aqueous solution interface Geochim. et Cosmochim. Acta 57 3505-3518
[10]  
Brady P. V.(1990)Temperature dependence of kaolinite dissolution Am. J. Sci. 290 797-910