For the pseudo-first-order model (n = 1), the integrated equation

For the pseudo-first-order model (n = 1), the integrated equation is: equation(5) qt=qe(1−ⅇ−k1t)qt=qe(1−ⅇ−k1t) Integration of the pseudo-second-order (n = 2) model leads to: equation(6)

qt=k2qe2t1+k2qet Evaluation of model ability to predict the experimental data was based on both regression correlation coefficient values (r2) and difference between experimental (qt,exp) and model-estimated (qt,est) values, evaluated by means of the error measure: equation(7) RMS(%)=100∑[(qt,est−qt,exp)/qt,exp]2/Nwhere N is the number of experimental points in each qt vs. t curve. Results for the non-linear fits of the kinetic models and their estimates for equilibrium adsorption capacity are shown in Table 4. The pseudo-second-order model provided selleck kinase inhibitor higher r2 values and lower values of RMS error in comparison to the pseudo-first-order model, thus being considered more adequate for description of the adsorption data, for all evaluated temperatures. This model has been successfully applied for description of adsorption kinetics of several adsorbates, describing both chemisorption and ion exchange ( Ho, 2006). It was also the more adequate model for description of Phe removal by DCAC

( Clark et al., 2012). Given the porous nature of CCAC (Section Selleckchem NVP-BGJ398 3.2), diffusion inside the pores was investigated according to the intra-particle diffusion model (Clark et al., 2012): equation(8) qt=kpt1/2+Cqt=kpt1/2+Cwhere kp is the intra-particle diffusion rate constant, evaluated as the slope of the linear portion of the curve qt vs. t1/2. Results for intra-particle diffusion are displayed in Fig. 5 and the corresponding calculated parameters are shown in Table 4.

If intra-particle diffusion is the rate-controlling step, the qt vs. t1/2 plot should be a straight line passing through the origin. However, this plot can present up to four linear regions, representing film diffusion, followed by diffusion in micro, meso, and macropores, and finally a horizontal line representing the adsorption equilibrium. An evaluation of curves in Fig. 5 shows that, for each value of initial concentration, Montelukast Sodium three distinct fitted lines can be identified, with variations in the overall qualitative behavior with the increase in Phe initial concentration and temperature. An increase in slope can be observed for the first two lines with an increase in initial concentration, this being attributed to the corresponding increase in the driving force for mass transfer between solution and adsorbent ( Clark et al., 2012). For Phe removal at 25 °C ( Fig. 5a), regardless of the initial Phe concentration, the first line passes through the origin, indicating that pore diffusion is an important mechanism.

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