||Impact of Oxygen Mediated Oxidative Coupling on Adsorption Kinetics.
Vidic, R. D. ;
Suidan, M. T. ;
Brenner., R. C. ;
||Environmental Protection Agency, Cincinnati, OH. Risk Reduction Engineering Lab. ;Cincinnati Univ., OH. ;Pittsburgh Univ., PA.
Water pollution control ;
Reaction kinetics ;
Surface chemistry ;
Activated carbon treatment ;
Granular activated carbon treatment ;
||Some EPA libraries have a fiche copy filed under the call number shown.
||The presence of molecular oxygen in the test environment promotes oxidative coupling (polymer formation) of phenolic compounds on the surface of granular activated carbon (GAC). Both adsorption equilibria and adsorption kinetics are affected by these chemical reactions. Lack of molecular oxygen interference with adsorption kinetics during the initial phase (first 12 h) of adsorbent-adsorbate contact, observed for the experimental conditions tested, can be explained by the lower rate of adsorbate polymerization when compared to the rate of pure adsorption. The homogeneous surface diffusion model (HSDM) adequately describes adsorption kinetics under anoxic conditions, but it fails to accurately predict experimental data collected in the presence of molecular oxygen. For the experimental conditions tested in the study, GAC particle size did not influence the magnitude of the surface diffusion coefficient. However, the increase in the initial adsorbate concentration yielded an increase in the surface diffusion coefficient. This may be attributed to a decrease in the adsorption forces for higher surface coverage.
||Pub. in Water Research, v28 n2 p263-268 1994. Prepared in cooperation with Cincinnati Univ., OH. and Pittsburgh Univ., PA.
|NTIS Title Notes
||Journal article 1990-93.
||Reprint: Impact of Oxygen Mediated Oxidative Coupling on Adsorption Kinetics.
||68D; 99C; 99F
||PC A02/MF A01