Adsorption of Chemically Prepared Cocoa Nibs Based Activated Carbon Onto Methylene Blue: Equilibrium and Kinetic Studies
1Faculty of Science and Technology, Universiti Sains Islam Malaysia, 71800 Nilai, Negeri Sembilan, Malaysia
2Jabatan Perubatan Forensik, Hospital Kuala Lumpur, 50586 Kuala Lumpur, Malaysia
3Cocoa Innovative and Technology Centre, Malaysian Cocoa Board, Lot 12621, 71800 Nilai, Negeri Sembilan, Malaysia
4Academy of Language Studies, Universiti Teknologi MARA Pahang, Bandar Tun Abdul Razak, Jengka, Pahang, Malaysia
5School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 NibongTebal, Penang, Malaysia
6Solid Waste Management Cluster, Science & Engineering Research Centre, Engineering Campus, Universiti Sains Malaysia, Nibong Tebal, Penang, Malaysia
*Corresponding author: Mohd Azmier Ahmad, Associate Professor, School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang, Malaysia, Tel: +604 5996459, Fax: +604 5996908, E-mail: email@example.com
Received: March 23, 2017 Accepted: April 4, 2017 Published: April 10, 2017
Citation: Nikman KA, Ahmad F, Hassan MS, Nikman K, Ahmad MA. Adsorption of Chemically Prepared Cocoa Nibs Based Activated Carbon Onto Methylene Blue: Equilibrium and Kinetic Studies. Int J Petrochem Res. 2017; 1(1): 15-18. doi: 10.18689/ijpr-1000104
Copyright: © 2017 The Author(s). This work is licensed under a Creative Commons Attribution 4.0 International License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
This study was aimed to prepare cocoa nibs based activated carbon (CNAC) via
chemical activation for methylene blue (MB) dye adsorption from aqueous solution. The
activation process was performed at 500°C under inert condition using K2CO3 as
activation agent. The effect of contact time and initial concentration of adsorbate on the
adsorption process were examined. Langmuir isotherm model fitted well the adsorption
equilibrium data with monolayer adsorption capacity of 64.98 mg/g at 30°C. The
adsorption kinetic was found to follow the pseudo-second-order kinetic model.
Keywords: Activated carbon, Chemical activation, Cocoa nibs, Methylene blue.
Water pollution has become a highlighted issue as some of the industrial effluent is
directly discharged into the river and water bodies without proper treatment . Dyes
effluent treatments from textile industries are divided into biological, physical and
chemical treatment processes. All these processes have different color removal
capabilities, capital costs and operating rates . Physical treatment via adsorption
process using Agrowaste based activated carbon as adsorbent is among the most
efficient and cheap method for dyes removal. Several studies on agrowastes have been
employed to remove the contaminants such as methylene blue (MB) dye from the water
bodies  . Agrowaste is appreciated as economical, sustainable and ecologically
friendly materials. In this study, an attempt was made to utilize cocoa nibs waste into
activated carbon using chemical activation process. The performance of CNAC was
studied in removing MB dye from aqueous solution.
All reagents and chemicals used in the research were analytical grade chemicals. For impregnation process, potassium carbonate (K2CO3) was used. Commercial methylene blue (C16H18ClN3S·3H2O) (MB) textile dye was obtained from Sigma-Aldrich (M) Sdn Bhd
Preparation of Stock and Test Solutions
Stock solution of MB with concentration of 500 mg/L was prepared by dissolving approximately 0.50 g of MB in 1000 mL distilled water. Test solution of MB ranging from 10 mg/L to 100 mg/L were prepared by subsequent dilution from stock solution.
Production of Pellet
The cocoa nibs waste was ground and sifted to a uniform size of 0.5 mm or smaller. The samples were shaped into pellets by compressing the mixture with a hydraulic press, in which the cocoa nibs were compacted into pellets with a specific density of 1.8 g/cm.
Preparation of Activated Carbon
The carbonization was performed by placing approximately 60 g of cocoa nibs pellet in a vertical furnace, which contained in a tubular stainless steel reactor. This step was carried outat 700°C for 1 hour under purified nitrogen (99.99%) with flowrate of 120 mL/min. Then, the furnace was allowed to cold to ambient temperature. Char yield was determined using following equation:
where is the mass of char after carbonization process and wi is the initial mass of cocoa nibs pellet. An amount of dried char was added with K2CO3 at various impregnation ratio (IR) in a 250 ml beaker. Both were mixed with deionized water to dissolve the salt. The IR was calculated as follows:
is the dry weight of potassium carbonate
pellets and wchar is the dry weight of cocoa nibs char. The mixture
was then dehydrated in an oven at 105°C for 24 hours. The
activation step was done using similar reactor as in carbonization
step but at final temperature of 500°C under nitrogen flowrate of
120 mL/min for 2 hours. The sample was then cooled to room
temperature and washed with hot deionized water until the pH
of the washed solution reached 6.5-7.
Removal of MB by Batch Adsorption Study
The batch equilibrium experiments of the adsorption capacity studies were conducted at 30 °C in a 250 mL conical flask in a water bath shaker. The stock solution (1000 mg/L) of MB was prepared by dissolving approximately weighed 1.0 gram of the MB in 1000 mL of distilled water in a 1500 mL volumetric flask. The stock solutions were stored in dark place to prevent direct sunlight. The sample solutions were withdrawn at equilibrium to determine the residual concentration. The concentrations of the filtrates were measured using UV-Visible Spectrophotometer (Model Agilent Cary 60, USA).
Effect of Initial Concentration
In order to study the effects of initial adsorbate concentration, 100 mL of adsorbate solutions with known initial concentration (10, 25, 50, 80, 100 mg/L of MB) were prepared in a series of 250 mL Erlenmeyer flasks. The amount of adsorbent that was added into each flask was fixed at 0.1 g. The flasks were placed in an isothermal water bath shaker at temperature and rotation speed of 30°C and 120 rpm, respectively until equilibrium point was reached.
Effect of Contact Time
In order to study the effects of contact time on the adsorption uptake, 100 mL of adsorbate solutions with known initial concentration (10-100 mg/L) were prepared in a series of 250 mL Erlenmeyer flasks. The amount of CNAC that was added into each flask containing MB solution was fixed at 0.1 g. The flasks were then placed in an isothermal water bath shaker of 30 °C with rotation speed of 120 rpm for 360 minutes. The percent removal of adsorbate was calculated as follows:
Where Ce is the concentration of adsorbate at equilibrium and Ci is the initial concentration of adsorbate. The MB uptake at equilibrium is calculated as follows:
where m is the mass of the adsorbent and V is the volume
of the adsorbate.
Adsorption isotherm study was carried out by fitting the equilibrium data to three isotherm model which are the Langmuir and Freundlich isotherm models, respectively represented by Equations (5),(6) and (7). The applicability and suitability of the isotherm equation to the equilibrium data was compared by judging the values of the correlation coefficients, R2. The Langmuir model is atypical model used to measure the amount of adsorbate on an adsorbent at equilibrium. The relation is expressed by following equation :
where, qe is the amount adsorbed (mg/g), Ce is the
equilibrium concentration of the metal ion (mg/L), qe is the
maximum amount of adsorbed metal ion per unit mass of
sorbent corresponding to complete coverage of the adsorptive
sites(mg/g), KL is the Langmuir constant related to the energy
The Freundlich adsorption isotherm or Freundlich equations are a relation between the concentrations of a solute on the surface of an adsorbent, to the concentration of the solute in the liquid with which it is in contact. The relationship is stated as follows :
In this equation, qe (mg/g) is amount of adsorbed material
in adsorbent surface k in arrangement are adsorption capacity
and adsorption intensification.
The kinetics of adsorption describes the rate of adsorbate uptake on activated carbon prepared and it controls the equilibrium time. The kinetics of adsorbate uptake is required for selecting optimum operating conditions for the full-scale batch process. Therefore, models for liquid-phase adsorption such as pseudo-first-order and pseudo-second-order were used to analyze the adsorption kinetic data. The pseudo-first-order kinetic model equation of Largergren  is generally expressed as:
Where qe is the amount of adsorbate adsorbed at equilibrium (mg/g), qt is the amount of solute adsorb per unit weight of adsorbent at time (mg/g), k1 is the rate constant of pseudo-first order sorption (1/h). The pseudo-second-order equation is expressed as :
Results and Discussion
Effect of contact time and MB initial concentration on
Figure 2 and Table 1 show the effect of various initial concentrations on adsorption of MB by CNAC. An equilibrium time of 100 min was needed for MB dye solution with initial concentrations of 10-25 mg/l to reach equilibrium. However, for initial concentrations of 50-100 mg/l, longer equilibrium times of 22-24 hours were required for the system to reach equilibrium. Initially, adsorbate molecules have to first encounter the boundary layer effect. Then it has to diffuse from boundary layer film onto adsorbent surface and finally, it has to diffuse into the porous structure of the adsorbent . The ratio of the initial number of dye molecules to the available surface area was low at lower initial concentration compared to higher initial concentration. Therefore, MB solution with higher initial concentration would take relatively longer contact time to attain equilibrium due to the higher amount of MB molecules.
Figure 2: Effects of contact time of MB onto CNAC
Table 1: MB percent removal by CNAC with IR 3:1
Effect of IR on adsorption equilibrium
Fig. 1 shows the influence of IR on CNAC in removing MB. Sample impregnated with 2:1 ratio has the lowest capability to adsorb the adsorbate where the value is 27.8 mg/g.
Figure 1: Effect of IR on MB uptake
The adsorption capacity of CNAC was decreased with
increased in IR from 1:1 to 2:1 before increased at IR of 3:1. CNAC with 3:1 ratio managed to adsorb 30.9 mg/g of MB at
equilibrium. Higher IR was favorable for enhancing the MB
adsorption as more pores are developed on the sample
The most appropriate correlation for the equilibrium curve needs to be established in order to understand the adsorption system. Therefore, the equilibrium adsorption data were analyzed using the Langmuir and Freundlich isotherms as shown in Figure 3 whereas Table 2 summarizes all the constants from both isoterm models.
Figure 3: Linear plots of (a) Langmuir and (b) Freundlich adsorption models
Table 2: Parameters of Langmuir and Freundlich adsorption isotherm for MB.
Langmuir model gave the highest R2 values which were
greater than 0.96. Conformation of the experimental data into
the Langmuir isotherm equation proved that the surface of
CNAC for MB adsorption was made up of homogeneous
adsorption patches with monolayer coverage of MB onto
CNAC . The monolayer saturation capacity of CNAC was
found to 64.98 mg/g at 30 °C.
All the experimental and calculated qe values obtained from the pseudo-first-order and pseudo-second-order kinetic model for adsorption of MB at 30 °C are tabulated in Table 3. Comparing the R2 values, pseudo-second-order model showed a significant agreement with adsorption mechanisms, which indicated the chemisorption with the heterogeneous active sites occurred on the surface of CNAC .
Table 3: Parameter values of the kinetic studies of the adsorption of MB onto CNAC.
CNAC was found to be suitable for the removal of MB from aqueous solution. Adsorption of MB was found to increase with increase in contact time and initial dye concentration. The Langmuir isotherm model was well described by the equilibrium data with maximum adsorption capacity of 64.98 mg/g. The pseudo-second-order kinetic model fits well with the kinetic data.
The authors are grateful for the funding from Solid Waste Management Cluster, USM (1001/CKT/870023) and research grant from Ministry of Science, Technology and Innovation (MOSTI), Malaysia.
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