Research Article

Heavy Metal Adsorption onto Kappaphycus sp. from Aqueous Solutions: The Use of Error Functions for Validation of Isotherm and Kinetics Models

Table 1

Equations of the isotherm, kinetic, and thermodynamic models used in the study.

ModelEquationReference

Langmuir[25]
[26]

Freundlich[27]

Temkin[28]

D-R[29]
[30]

PFO[31]

PSO[32]

Elovich[28]
[33]

IpD[34]

Thermodynamics[35]

(mg L−1): adsorbate initial concentration, (mg L−1): adsorbate equilibrium concentration, (mg g−1): observed biosorption capacity at equilibrium, (mg g−1): maximum biosorption capacity, (L mg−1): Langmuir constant related to the energy of adsorption, (): a dimensionless constant, known as separation factor, (mg g−1) (L mg−1): Freundlich isotherm constant related to the sorption capacity, : a constant which gives an idea of the grade of heterogeneity, (8.314 J mo−1): universal gas constant, (°K): absolute temperature, (L mg−1): equilibrium binding constant corresponding to the maximum binding energy, (J mol−1): Temkin constant related to heat of sorption, (mol2 kJ−2): Dubinin-Radushkevich isotherm constant, : Polanyi potential related to the equilibrium concentration, (kJ mol−1): mean free energy of biosorption, (mg g−1): equilibrium adsorption uptake at time, , (min−1): pseudo-first-order rate constant of adsorption, (g mg−1 min−1): pseudo-second-order rate constant of adsorption, (mg g−1 min−1): initial adsorption rate, (min): half-adsorption time, (mg g−1 min−1): initial adsorption rate constant, β (g mg−1): desorption constant, (mg g−1): boundary layer diffusion effect, (mg g−1 min−0.5): rate constant for intraparticle diffusion, (kJ mol−1): change in Gibbs free energy, (kJ mol−1): change in enthalpy, (kJ mol−1 K−1): change in entropy, and : thermodynamic equilibrium constant.