skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Theoretical prediction of single-site surface-protonation equilibrium constants for oxides and silicates in water

Journal Article · · Geochimica et Cosmochimica Acta
;  [1]
  1. Johns Hopkins Univ., Baltimore, MD (United States)

The equilibrium constants for surface protonation of solid oxides and silicates can be estimated from theoretical considerations and known properties of the solids for use in the constant capacitance, diffuse double layer or triple layer models of surface complexation. The theoretical considerations take into account Born solvation theory for the adsorbing proton, electrostatic interactions of the adsorbing proton with a surface oxygen and an underlying metal, and an intrinsic binding of the proton to the surface. As a consequence, the equilibrium constants for the {nu}th ({nu} = 1 or 2) surface protonation reaction on the kth solid can be expressed in terms of the inverse of the dielectric constant of the solid (1/{epsilon}{sub k}) and an average Pauling bond strength per angstrom (s/r{sub M-OH}) for the solid according to log K{sub {nu}} = M{sub {nu}}(1/{epsilon}{sub k}) - B{sub {nu}}(s/r{sub M-OH}) + log K{sub ii,{nu}}{sup {double_prime}}, where the coefficients M{sub {nu}} B{sub {nu}} and K{sub ii{nu}}{sup {double_prime}} are constants characteristic of all oxides and silicates for each surface complexation model. Evaluation of these constants using experimental data for TiO{sub 2}, {gamma}-alumina, Al{sub 2}O{sub 3} FeOOH, Fe(OH){sub 3}, silica, quartz. and kaolinite permits widespread prediction of surface protonation equilibrium constants from the known bulk structure properties 1/{epsilon}{sub k} and s/r{sub M-OH}. Such predictions should replace attempts to estimate surface protonation equilibrium constants for solids from empirical correlations with aqueous equilibrium constants. Surface protonation constants should also not be estimated from correlations with only the Pauling bond strength because these neglect specific treatment of salvation. 92 refs., 14 figs., 4 tabs.

DOE Contract Number:
FG02-96ER14616
OSTI ID:
577435
Journal Information:
Geochimica et Cosmochimica Acta, Vol. 60, Issue 20; Other Information: PBD: Oct 1996
Country of Publication:
United States
Language:
English

Similar Records

Theoretical prediction of single-site enthalpies of surface protonation for oxides and silicates in water
Journal Article · Tue Dec 01 00:00:00 EST 1998 · Geochimica et Cosmochimica Acta · OSTI ID:577435

Recalculation, evaluation, and prediction of surface complexation constants for metal adsorption on iron and manganese oxides
Journal Article · Fri Mar 01 00:00:00 EST 1991 · Environmental Science and Technology; (USA) · OSTI ID:577435

Evaluation of internally consistent parameters for the triple-layer model by the systematic analysis of oxide surface titration data
Journal Article · Tue Jul 01 00:00:00 EDT 1997 · Geochimica et Cosmochimica Acta · OSTI ID:577435