Calcium adsorption at the rutile-water interface:: A potentiometric study in NaCl media to 250°C

被引:52
作者
Ridley, MK
Machesky, ML
Wesolowski, DJ
Palmer, DA
机构
[1] Illinois State Water Survey, Champaign, IL 61820 USA
[2] Oak Ridge Natl Lab, Chem & Analyt Sci Div, Oak Ridge, TN 37831 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/S0016-7037(99)00236-7
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Calcium adsorption by rutile was studied potentiometrically from 25 to 250 degrees C, at ionic strengths of 0.03 and 0.30 m in NaCl media, using two complementary experimental methodologies. In the first, net proton adsorption in the presence and absence of Ca2+ was monitored, and in the second, samples were periodically withdrawn during the course of a titration to determine Ca2+ adsorption directly. These experiments revealed that Ca2+ adsorption systematically increased with temperature relative to the pH of zero net proton charge in NaCl media alone (pH(znpc(NaCl)) - pH). That is, as temperature increased, Ca2+ adsorption commenced at progressively more positive pH(znpc(NaCl)) - pH values. Increasing ionic strength from 0.03 to 0.30 m NaCl suppressed Ca adsorption at all temperatures as a result of either increased competition from Na+ or greater complexation of Ca2+ by Cl-. Finally, there was no apparent trend in the proton stoichiometric ratios (moles H+ released / moles Ca2+ adsorbed) with increasing temperature. This suggests that the electrostatic and/or chemical processes involved in Ca2+ adsorption do not change greatly with increasing temperature. Favorable entropic effects, related to the increasing ease of releasing Ca2+ waters of hydration, are believed to be primarily responsible for the increase in adsorption with temperature. Copyright (C) 1999 Elsevier Science Ltd.
引用
收藏
页码:3087 / 3096
页数:10
相关论文
共 43 条
[1]  
ANGROVE MJ, 1998, J COLLOID INTERF SCI, V204, P93
[2]  
[Anonymous], ADSORPTION INORGANIC
[3]   ADSORPTION FROM MIXTURES CONTAINING MONO-VALENT AND BIVALENT-CATIONS ON INSOLUBLE OXIDES AND A REVISION OF THE INTERPRETATION OF POINTS OF ZERO CHARGE OBTAINED BY TITRATION [J].
ARDIZZONE, S ;
FORMARO, L ;
LYKLEMA, J .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1982, 133 (01) :147-156
[4]  
BARGAR JR, 1997, HGEOCHIM COSMOCHIM A, V62, P193
[5]   A BRIEF DISCUSSION ON THE EFFECT OF TEMPERATURE ON THE REACTION OF INORGANIC-IONS WITH SOIL [J].
BARROW, NJ .
JOURNAL OF SOIL SCIENCE, 1992, 43 (01) :37-45
[6]   A FRAMEWORK FOR ANALYZING THE CONTRIBUTION OF EDUCATIONAL-TECHNOLOGY TO LEARNING [J].
BERGEN, C ;
KINGSTON, P .
BRITISH JOURNAL OF EDUCATIONAL TECHNOLOGY, 1994, 25 (01) :58-60
[7]   ADSORPTION AT RUTILE-SOLUTION INTERFACE .I. THERMODYNAMIC AND EXPERIMENTAL STUDY [J].
BERUBE, YG ;
DEBRUYN, PL .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1968, 27 (02) :305-&
[8]   SURFACE-ACIDITY OF METAL-OXIDES IMMERSED IN WATER - A CRITICAL ANALYSIS OF THERMODYNAMIC DATA [J].
BLESA, MA ;
MAROTO, AJG ;
REGAZZONI, AE .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1990, 140 (01) :287-290
[9]   ALUMINA SURFACE-CHEMISTRY AT 25, 40, AND 60-DEGREES-C [J].
BRADY, PV .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1994, 58 (03) :1213-1217
[10]   THERMODYNAMIC QUANTITIES FOR IONIZATION OF WATER IN SODIUM-CHLORIDE MEDIA TO 300-DEGREES-C [J].
BUSEY, RH ;
MESMER, RE .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 1978, 23 (02) :175-176