[Adsorption Characteristics of Arsenite on Goethite by Flow Stirring Method]

Adsorption characteristics of arsenite on goethite under the effects of the solution pH, concentration and temperature were investigated using a flow-stirring dynamic device. The results showed that the adsorption process of arsenic could be divided into rapid and slow reactions under different conditions.The maximum of arsenite adsorption fitted by the first order equation remarkably decreased with increase in the solution pH, for example, 246.9 mg·kg^-1 at pH 3.0 and 99.8 mg·kg^-1 at pH 7.0, respectively. The rate constant(k')of the apparent adsorption increased gradually along with the increase of solution pH, and so the half reaction time(t)was smaller, and the equilibrium time of arsenic adsorption was shorter. At the same time, the b values of diffusion rate constant were reduced gradually. With the increase of arsenic concentration, the amounts of arsenic adsorption and the k' values increased gradually. The maximum amount of adsorption of arsenic was 96.5 mg·kg^-1 and 249.1 mg·kg^-1 when the arsenic concentration was 0.10 mg·L^-1 and 1.00 mg·L^-1, respectively. Adsorption constant(K_f)by the Freundlich equation decreased gradually with the extension of the reaction time and its ability of adsorption was gradually weakened. Distribution factor(R_L)by Langmuir equation was between 0-1, and the adsorption of arsenic on goethite was accounted for the preferential adsorption. With the increase of temperature, the maximum amount of adsorption of arsenic was increased, for example, 241.1 mg·kg^-1 at 298 K and 315.6 mg·kg^-1 at 313 K, respectively. And the k' values of the apparent adsorption rate constant gradually rose in the meantime. The false thermodynamic constants were calculated using the b values of the diffusion rate by the parabolic diffusion equation. The reaction activation energy(E_a^*)of Arsenic adsorption was 14.60 kJ·mol^-1. The change of arsenic diffusion activation enthalpy(ΔH^θ)decreased with the increase of temperature, and ΔH^θ was positive in values and on behalf of the endothermic process. So the rising temperature was beneficial to the diffusion of arsenic. ΔG^θ of activation free energy was increased as the temperatures rose, and helpful to accelerate the diffusion process. Entropy of activation(ΔS^θ)was negative in all cases, suggesting that the system could improve its degree of order.