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Adsorption of Reactive Dyes by Palm Kernel Shell Activated Carbon: Application of Film Surface and Film Pore Diffusion Models
M. M. NOUROUZI, T.G. CHUAH* and THOMAS S.Y.CHOONG Department of Chemical and Environmental Engineering, Faculty of Engineering, Universiti Putra, Malaysia, 43300 UPM Serdang, Selangor, Malaysia.
chuah@eng.upm.edu.my Received 1 October 2008; Revised 17 February 2009; Accepted 15 March 2009 Abstract: The rate of adsorption of two reactive dyes, Reactive Black 5 and Reactive Red E onto palm kernel shell-based activated carbon was studied. The experiment was carried out to investigate three models: film diffusion model, filmsurface and film-pore diffusion models. The results showed that the external coefficients of mass transfer decreased with increasing of initial adsorbate concentration. In addition, it was found that the adsorption process was better described by using the two resistance models, i.e. film-surface diffusion. Keywords: Adsorption, Reactive dye, Palm kernel shell, Film-surface-pore diffusion.
Introduction
Industries, such as textile, ceramic, paper, printing and plastic, use dye as their raw material, thus generating a large amount of colored wastewater. Adsorption methods are promising in decolorizing textile effluents, but this application is limited by the high cost of adsorbents. The activated carbon derived from agricultural wastes is important due to the fact that it is inexpensive, adequate to remove organic and inorganic contaminants from wastewater and locally available1. Malaysia is a major producer of palm oil. In 2002 alone, the amount of palm kernel shell generated in Malaysia was approximately 4.3 million tons which can cause serious disposal problem2. Considering the volume of this waste, several studies were initiated to utilize Palm Kernel Shell as the crude material for activated carbon and it is reported that a good quality product can be obtained, such as its granular structure, insolubility in water, chemical stability and high mechanical strength2,3. It is important to be able to predict the rate at which pollutant is removed from aqueous solutions in order to design appropriate sorption treatment plants. Therefore, the kinetics that describes the dye uptake rate needs to be determined. The adsorption mechanism can be described by three essential steps4:
950 1.
External mass transfer from bulk solution to adsorbent surface across the boundary layer surrounding the adsorbent surface particle. 2. Intraparticle diffusion within the internal structure of particle. Internal diffusion is diffusion of molecule inside the pores and surface diffusion is diffusion of the molecules on surface phase. 3. Adsorption at an interior site. Generally, the total rate of the kinetic process is controlled by the rate of the slowest process. The transport of the adsorbate from the bulk of fluid phase to the external surface of adsorbent forms an important step in the uptake process. Single resistance models involve only a liquid film resistance, pore diffusion resistance or surface diffusion resistance5. In most cases, single resistance models are not adequate to explain the adsorption process for porous adsorbents. Therefore, two resistance mass transfer models which incorporate both external and intraparticle diffusion effects is applied6. Two resistance models can be divided into: 1. Film-pore diffusion model. 2. Film-surface diffusion model. A model which incorporated film, pore diffusion and concentration dependent surface diffusion was introduced7 and later on a three-resistance model based on external mass transfer, pore and concentration dependent surface diffusion for removal of methylene blue by PKS based-AC was presented8. They expressed that the film-pore-concentrationdependent surface diffusion (FPCDSD) model was able to fit the experimental data using a single set of mass transfer parameters for a wide range of initial dye concentrations. However, a two resistance model may be easier for implementation.
Experimental
PKS-based activated carbon supplied from KD Technology Sdn. Bhd was used without any chemical or physical treatment. Two reactive dyes were used for this investigation, namely, Reactive Black 5 (RB 5) and Reactive Red E (RR E) supplied from Texchem-Pack Bhd. The chemical structure of these dyes is given in Table 1. According to data obtained from pH meter, for single solution pH of the solution of RB 5 and RRE was 6.5 and 6.4, respectively. For binary solution, treating both dyes RB 5 and RR E in one solution, pH was 6.4. To prepare the stock solution, 1.000 g (+0.0005) of each dye was dissolved in 1 L distilled water. In order to maintain homogenous condition, the solution was shaken for 5 hours using orbital incubator shaker (Sepilau Saintifik, Malaysia) at 28oC. Then the solution was kept in dark place for avoiding any off-color due to sunlight. The stock solution would then be diluted into desired concentration.
Adsorption of Reactive Dyes by Palm Kernel Shell Activated Carbon Table 1. Properties of RB 5 and RR E9. Type Chemical structure C.I. Reactive Black 5 Reactive dye C.I. Reactive Red E Reactive dye
951
Vdcb Mdq = dt dt
(2) (3)
3M app
where q is average adsorbed-phased concentration, M is mass of adsorbent, V is volume of solution, ap is particle radius and p is pellet density. The concentration of adsorbate, q , with respect to time is related to the mass transfer coefficient kf by: (4) 3k f dq = (c b c s ) dt a p p Equation 4 can be solved with appropriate initial condition: (5)
cb = c bo and q s = 0, t < 0
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3k f 3 D s q = (cb c r = a p ), a p r a p p
t0
The external mass transfer coefficient, kf, is estimated from the single-resistance model. To calculate the value of the solid phase diffusivity, Ds, equation 6 was solved numerically, considering the value of kf obtained from single-resistance model.
Film-pore diffusion
Pore diffusion equations are described as follow:
p
c q D p 2 c + p = 2 (r ), t t r r r c = 0, q = 0, 0 r a p 0 r ap
t<0
c = 0, r = 0, r
k f (cb c ) = D p ( c r ),
t0
r = ap, t0
where Dp is pore diffusivity. Both the two resistance models were solved by using finite-difference method, as approximating the spatial derivation by central difference expression.
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Some values of the surface diffusivity, reported in other literature are listed in Table 3, as well. It can be seen that the values of Ds ranges between 1.510-9 to 1.510-10 cm2/s. From Table 3, it can be noted that the values of Ds for RB 5 and RR E are different from values of other literatures. The difference shows specificity of adsorption. In other word interaction between adsorbate and adsorbent is characteristic for each system and it is not common for all systems13. Table 3. Values of Ds, reported in the literature on adsorption of different dyes using different adsorbents and this work. Surface Diffusivity, cm2/s Reference 14 1.510-10 15 1.510-9 This work. 110-6 This work. 910-7 Figures 1(a) and 1(b) show the comparisons of results of both adsorptions of RB 5 and RR E onto PKS-based activated carbon with predictions based on the film-surface diffusion and film-pore diffusion models. It is obvious from these figures that prediction based on the film-surface diffusion model fits better with experiment data than the film-pore diffusion model, and it agrees with both dyes. The values of SSE for film-surface diffusion are significantly less than values of SSE for film-pore diffusion, as shown in Table 5. As a result, it indicated that the adsorption process was governed by the resistance models, i.e. film-surface diffusion mechanism. The values of Dp are as listed in Table 4. Material Filtrasorb-400 AC Filtrasorb-400 AC PKS-AC PKS-AC Dye Cibacron reactive red Tectilon Red 2B RB 5 RR E
1 0.9 0.8 0.7 Cb/Cbo 0.6 0.5 0.4 0.3 0.2 0.1 0 0 20 40 60 80 100 120 140
20 mg/L S.D 20 mg/L Exp data 20 mg/L P.D
Cb/Cbo
Time, h
Figure 1(a). Comparison between prediction of film-surface diffusion (S.D) and film-pore diffusion (P.D) models with experiments data from adsorption of RB 5 onto PKS-based activated carbon at dye concentration of 20 mg/L and dosage of adsorbent 2 g/L (single system).
1 0.9 0.8 0.7
20 mg/L S.D 20 mg/L Exp data 20 mg/L P.D
Cb/Cbo
Cb/Cbo
0.6 0.5 0.4 0.3 0.2 0.1 0 0 50 100 150 200 250
Time, h
Figure 1(b). Comparison between prediction of film-surface diffusion (S.D) and film-pore diffusion (P.D) models with experiments data from adsorption of RR E onto PKS-based activated carbon at dye concentration of 20 mg/L and dosage of adsorbent 2 g/L (single system).
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T.G. CHUAH et al. Table 4. Values of Dp for adsorption of RB 5 and RR E onto PKS based-AC. Kinetic Model RB 5/PKS RR E/PKS
2 D p , cm /s
2.410-7 4.710-8
Table 5. Comparison of SSE of film-surface diffusion and film-pore diffusion models for adsorption of RB 5and RR E onto PKS based-AC. Kinetic model RB 5/PKS RR E/PKS SSE Film-surface diffusion Film-pore diffusion 13.9 153.6 4.5 101.6
Conclusion
The rate of the kinetic process for both dyes was better described by two resistance models. Based on SSE, the film-surface diffusion model was able to fit experimental better than the film-pore diffusion model for both RB 5 and RR E on palm kernel based activated carbon.
Acknowledgement
The authors are grateful to KD Technology Sdn. Bhd. for supplying granular PKS.
References
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