Table 2.
Eq. | Kinetic equations | ||
---|---|---|---|
5 | PFO |
: the calculated adsorption capacity at any time t (mg g−1) k1: the PFO rate constant of adsorption (min−1) |
|
6 | PSO | k2: the PSO rate constant of adsorption (g mg−1 min−1): the initial adsorption rate (mg g−1 min−1) | |
7 | Elovich | α: the initial adsorption rate (mg g−1 min−1)β: kinetic parameter related to the activation energy for chemisorption and extent of surface coverage (g mg−1) | |
8 | IPD | kIPD: intra-particle diffusion rate constant (mg g−1 min−0.5)C: intra-particle diffusion constant related to the thickness of the boundary layer (mg g−1) | |
Isotherm equations | |||
9 | Langmuir |
: the theoretical maximum adsorption capacity (mg g−1) KL: the Langmuir equilibrium constant (L mg−1) RL (): the separation factor (−) |
|
10 | Freundlich |
KF: Freundlich constant ((mg g−1) (L mg−1)1/n) n: adsorption intensity (−) |
|
11 | R-P |
KR−P: Redlich-Peterson isotherm constant (L g−1) αR−P: Redlich-Peterson isotherm constant (mg L−1)−g g: Redlich-Peterson isotherm binding constant (0 < g < 1) |
|
Thermodynamic equations | |||
12 |
: thermodynamic equilibrium constant (−) MW: the molecular weight of the adsorbate (g mol−1) [absorbate]°: the unitary standard concentration of the adsorbate (1 mol L−1) γ: the coefficient of activity (−) |
||
13 |
R: the universal gas constant (J mol−1 k−1) : standard enthalpy changes of adsorption (kJ mol−1) : standard entropy changes of adsorption (J mol−1 K−1) |
||
14 | : standard Gibbs free changes of adsorption (kJ mol−1) |