Abstract:Energy characteristics of the reaction kinet ics of H+ -Ca2+ on red soil surface under acidic conditions were investigated by using a home-made dynamic device.The results showed that Ca2+ adsorption could be divided into rapid and slow reactions.The maximal Ca2+ adsorption fitted by the first order equation remarkably decreased with increase in acidity and reached equilibrium in advance with increase in temperature.A two-constant equation could be used to describe unevenness of the energy distribution of Ca2+ adsorption on the sites of the soil surface.Activation energy(Eb) of Ca2+ diffusion was calculated by using b value of the rate constant of Parabolic Diffusion Low and increased with increase in acidity,which reflected that the energy barrier to be overcome by Ca2+ diffusion would rise up and the rate of diffusion in Ca2+ adsorption decrease accordingly.Enthalpy of activation(H) was positive in value and rising temperature could contribute to Ca2+ diffusion.Entropy of activation(S*) was nagative in all cases,suggesting that system could improve its degree of order.pH of effluent drast ically dropped when the influent solution was pH 4.5 and pH 5.6.H+ release could be best described by the first order equation and the power-function equation,which were followed by Elovich equation,Parabolic Diffusion Low and zero order equation.Energy barrier to be overcome by H+ (Al3+) diffusion in pH 5.6 treatment was lower than that in pH 4.5 treatment.△H values of H+ diffusion were positive indicating an endothermic reaction and the increase in temperature speeded up H+ diffusion.There was the consumption process of H+ ion by using influent of pH 3.5,which was attributed to soil buffer mechanism and specific adsorption of SO42-.The energy of activation of H+ consumption was lower than that of H+ release,showing that more H+ was diffused to the surface of soil particles than H+ released to bulk solution when the amount of H+ in the bulk solution exceeded a certain quantity.H+ consumption was rapid at the initial stage of the reaction.△H of H+ consumption,in comparison with that of H+ release,could contribute to H+ adsorption.Since H+ dissolution of minerals became a controlling process,it could be best described by Elovich equation and Parabolic Diffusion Low.