The kinetics and mechanism of methylene blue adsorption onto raw pine cone biomass (Pinus radiata) was investigated under various physicochemical parameters. The extent of the methylene blue dye adsorption increased with increases in initial dye concentration, contact time and solution pH but decreases with the amount of adsorbent, salt concentration and temperature of the system. Overall the kinetic studies showed that the methylene blue adsorption process followed pseudo-second-order kinetics among various kinetic models tested. The different kinetic parameters including rate constant, half-adsorption time and diffusion coefficient are determined at different physicochemical conditions. Equilibrium data were best represented by Langmuir isotherm among Langmuir and Freundlich adsorption isotherm. The maximum monolayer adsorption capacity of pine cone biomass was 109.89 mg/g at 30°C. The value of separation factor, R L , from Langmuir equation and Freundlich constant, n, both give an indication of favourable adsorption. Thermodynamic parameters such as standard Gibbs free energy (ΔG 0 ), standard enthalpy (ΔH 0 ), standard entropy (ΔS 0 ) and the activation energy (A) were calculated. A single-stage batch absorber design for the methylene blue adsorption onto pine cone biomass has been presented based on the Langmuir isotherm model equation.
Nomenclature
AActivation energy of adsorption (kJ/mol) C f Final metal ion concentration, ppm (mg/l) C 0 Initial metal ion concentration, ppm (mg/l) C t Metal ion concentration at time t, ppm (mg/l) D Diffusion coefficient (cm 2 /s) ΔG 0 Gibbs free energy change (kJ/mole) ΔH 0 Enthalpy change (kJ/mole) ΔS 0 Entropy change (J/k mole) k 1 Pseudo-first-order rate constant (min −1 ) k 2 Pseudo-second-order rate constant (mg/g min) K f Freundlich adsorption constant (mg/g) K idIntra-particle rate constant [(mg/g) min 0.5 ] MMass of adsorbent per unit volume (g l −1 ) m Amount of adsorbent added (g) n Freundlich constant q Amount of adsorbate per gram of adsorbent (mg/g) q e Amount of adsorbate per gram of adsorbent at equilibrium, (mg/g) q tAmount of adsorbate per gram of adsorbent at any time, t q m Equilibrium adsorption capacity using model q max Maximum adsorption capacity (mg/g) R 2Linear correlation coefficient Water Air Soil Pollut (2011) 218:499-515