Skip to main content
. 2022 Jun 22;12(8):185. doi: 10.1007/s13201-022-01703-6

Table 1.

Types of adsorption equations

Isotherm Equation
Single component dsorption q=(Co-Cf)Vm
Langmuir isotherm qe=qmKLCe1+KLCe
Brunauer-Emmett eller (BET) isotherm 1WP0P-1=1WmC+C-1WmCP0P
Freundlich isotherm qe=KFCe1n
Gibbs isotherm dγ=-niAdμi
Temkin Isotherm qe=RTBTlnATCe
Dubinin-Radushkevich DRK) isotherm qe=qsexp(-Kadε2)

Here q = the metal concentration retained in the sorbent phase (mg/g); C0 = the initial concentrations of the metal ion in solution (mol/l); Cf = the initial and final concentrations of the metal ion in solution (mol/l); V = the solution volume (liters); m = the mass of sorbent (g); qe = the quantity of metal adsorbed on the surface of the adsorbent (mg/g); Ce = the amount of metal present in the solution at equilibrium condition (mg/L); qm = the maximum adsorption capacity of the adsorbent (mg/g); KL = the Langmuir constant related to energy of adsorption (L/mg); KF = the Freundlich constant; W = weight of gas adsorbed; P/P0 = relative pressure; Wm = weight of adsorbate as monolayer; C = BET constant; γ = interfacial tension; (ni/A) = the number of moles of component adsorbed per unit area; μi = the chemical potential of the surfactant solution; AT = Temkin isotherm equilibrium binding constant (L/g); BT = Temkin isotherm constant; R = universal gas constant (8.314 J/mol/K); T = Temperature (K); qs = theoretical isotherm saturation capacity (mg/g); Kad = Dubinin–Radushkevich isotherm constant (mol2/kJ2) and ε = Dubinin–Radushkevich isotherm constant