20+ Million Readerbase
Indexed In
  • Open J Gate
  • Genamics JournalSeek
  • Ulrich's Periodicals Directory
  • RefSeek
  • Directory of Research Journal Indexing (DRJI)
  • Hamdard University
  • EBSCO A-Z
  • OCLC- WorldCat
  • Proquest Summons
  • Scholarsteer
  • Publons
  • Geneva Foundation for Medical Education and Research
  • Euro Pub
  • Google Scholar
Share This Page
Recommended Webinars & Conferences

27th Global Congress on Biotechnology

Paris, France

27th European Biotechnology Congress

Rome, Italy
Journal Flyer
Flyer image

Research Article - (2017) Volume 7, Issue 2

Carbon Nanotubes: Mechanism, Langmuir Hinshelwood Growth Kinetics and It Application for the Removal of Chromium (VI)

Ahmed A1*, Abdulhakim SA2, Ishaq K3, Saka AA3, Peter MS1 and Chidinma OU1
1Department of Chemical Sciences, Federal University Wukari, P.M.B. 1020, Wukari, Taraba State, Nigeria
2Department of Mathematic and Statistics, Federal University Wukari, P.M.B. 1020, Wukari, Taraba State, Nigeria
3Chemical Engineering Department, Federal University of Technology Minna, P.M.B. 65, Minna, Niger State, Nigeria
*Corresponding Author: Ahmed A, Department of Chemical Sciences, Federal University Wukari, P.M.B. 1020, Taraba State, Nigeria, Tel: +2348033576652 Email: ,

Abstract

In this study, kinetic model for decomposition of acetylene for the production of carbon nanotubes (CNTs) have been explored. The kinetics model described the CNTs growth in the chemical vapour deposition (CVD) reactor while Arrhenius equation was employed for the determination of the activation energy. The result of the analysis shows activation energy of 237.2483 kJmol-1 which is an indication that the reaction that leads to the production of CNTs is adsorption inclined. The observed frequency factor shows that the reactants’ particles collide at faster rate which enhances CNTs growth. The prepared CNTs were characterized using high resolution scanning electron microscope/high resolution transmission electron microscope (HRSEM/HRTEM), selected area electron diffraction (SAED), energy dispersive spectroscope (EDS) and Brunauer Emmett Teller (BET) method for morphology, crystallinity, elemental composition and surface area. CNT with best physiochemical properties was used to investigate effect of CNTs dosage, pH, contact time and temperature on percentage removal of chromium (VI). The pseudo first and second order rate equations were tested on kinetic data and the pseudo fist order rate kinetics best described the adsorption process. The equilibrium data shows satisfactorily fitted the Langmuir isotherm (R2=0.9914) than the Freundlich isotherms (R2=0.09758), Dubinin- Radushkevich isotherms (R2=0.9092) and Temkin isotherm (R2=0.9355).

Keywords: Carbon Nanotubes; Chemical Vapour Deposition; Langmuir Hinshelwood Kinetic Model; Adsorption Study

Introduction

Heavy metal pollution has been the main concern of many researchers for many years because of their toxicity towards the quality of life and the environment as whole [1-4]. Research have shown that continuous exposure to low levels of heavy metals may resulted in bioaccumulation and resulting health consequences in humans [5]. Chromium is one of the most poisonous heavy metal ions which are discharge with effluents of industries such as metallurgical, electroplating, leather tanning and others [6]. Accumulation of this metal in the human body can lead to some diseases such as cancer in the lung, allergic skin irritations, epigastria pains, vomiting and nausea [7]. Chromium can occur in an oxidation state of trivalent or hexavalent depending on it source. But research has shown that chromium (VI) is far more toxic than chromium (III) [8]. Amongst the methods available for removing chromium pollutant from aqueous effluent includes; electrochemical treatment, chemical precipitation, reverse osmosis, membrane technologies, adsorption process on adsorbent and various biological processes [9-11].

Most of these methods are not widely acceptable because of their inapplicability to a wide range of pollutants, high cost of operation and low efficiency [12]. The adsorption process is arguably one of the promising methods for the removal of heavy metal ions because of it flexibility, reliability, low cost of operation and having the capacity to regenerate the exhausted adsorbent. Ever since the discovery of carbon nanotubes (CNTs) in the early 1991 by Iijima, it applications in the removal of pollutants have attracted substantial interest in the scientific community due to its extraordinary structures in terms of large diameter and length/diameter ratio, unique electrical and thermal properties as well as mechanical strength in the field of material science engineering [13].

Although, several methods such as arc discharge [14], flame or laser ablation [15,16], and chemical vapour deposition (CVD) [17-21], have been reported for the synthesis of CNTs. The CVD method is considered one of the most dominant, ideal, cost effective, versatile, transferable method of producing high quality and large quantity CNTs at relatively low synthesis temperature [22]. This method gives the opportunity of modifying multi-structural parameters such as diameter, length and alignment in order to obtain a well-defined and organized array of CNTs with different morphology for a specific area of application [23]. However, the understanding of the growth kinetics of CNTs is the key to develop its prospective applications [24,25]. Therefore, information on the kinetic study of CNTs in the CVD reactor is the subjects of this study.

The information about the kinetic study of CNTs can be deduced by observing the variation in mechanism of the decomposition of hydrocarbon over time. Losurdo et al. [26] explored low pressure CVD kinetics in a real-time monitoring by using methane (CH4) and hydrogen has (H2) as carbon sources on two polycrystalline metal substrates of copper (Cu) and nickel (Ni) catalysts at a reaction temperature of 900°C, with the aim of investigating the role of H2 in distinguishing CNTs kinetics growth. From their findings, it was reported that H2 slows down the deposition kinetics of CNTs on Cu by blocking the active sites on the Cu surface, which resulted in poor quality morphology of the CNTs grown. On the other hand, Bi et al. [26,27] reported the direct synthesis of CNTs on dielectric substrates by ambient pressure CVD at a temperature range between 1100 to 1200°C using a gas mixture of CH4, H2 and Ar as the carrier gas. Their finding revealed the possibility of the formation of CNTs at a high temperature of about 1200°C over Si, SiO2 and Al2O3 substrates.

In this study, high quality CNTs growth using CVD method and the growth kinetics and mechanism of formation is reported. Fe-Ni catalyst over a kaolin substrate using wet impregnation method was used for the deposition of acetylene (C2H2) carbon source using Ar as a carrier gas. Also, the activation energy and the frequency factor of the C2H2 decomposition were reported using measured gas phase concentrations in the CVD reactor while the structural morphology of the prepared CNTs were studied using high resolution scanning electron microscope (HRSEM), selected area electron diffraction (SAED), high resolution transmission electron microscope (HRTEM), energy dispersive spectroscope (EDS) and Brunauer Emmett Teller (BET) surface area analyzer. Also, the CNTs with best structural morphological property were used study the effect of dosage, contact time, pH and temperature on the percentage removal of chromium (VI). Furthermore, the kinetic and adsorption isotherms were explored to establish the best fitted model with the adsorption study.

Materials and Methods

Materials

The acetylene and Argon gases were sourced from BOC Nigeria and they were of analytical grade with percentage purity of 99.99%. Chemicals used in this study include anhydrous potassium dichromate (VI), sodium hydroxide (OH), and hydrochloric acid (HCl) which were obtained from Sigma Aldrich and they were all of analytical grade with percentage purity in the range of 98-99.99%.

Methods

Production of MWCNTs: The catalyst used, which was thoroughly characterized in earlier studies, had a BET surface area of 3.76 m2/g, pore volume of 1.9 × 10-3 cm3/g and pore size of 0.5986 nm. The HRTEM of the catalyst also show lattice fringes of 0.3 nm with estimated catalyst particle size of 29-31 nm.

The experimental set-up consists of quartz boat (11 cm × 2.6 cm) containing 0.5 g of catalyst, placed at the center of the glass quartz tube as shown in Figure 1. The furnace around the glass quartz tube was heated at 10°C/min while argon (Ar) was flowing over the system at 30 mL/min to create an inert environment before the reaction time. After the purging of the system from room temperature to 700°C, the Ar flow rate was adjusted to 230 mL/min and C2H2 was then introduced at flow rate of 150 mL/min for reaction period of 45 minutes. A sampling probe was used to collect sampling gas which was directly introduced to gas chromatograph (GC) for chemical analysis. The growth experiment was stopped after 45 minutes reaction time by switching off the C2H2 gas, while the furnace was allowed to cool down to room temperature under a continuous flow of argon at a flow rate of 30 mL/min. The quartz tube was disconnected from the setup and the quartz boat was removed and the CNTs deposit was characterized using high resolution scanning electron microscope (HRSEM), selected area electron diffraction (SAED), high resolution transmission electron microscope (HRTEM), energy dispersive spectroscope (EDS) and Brunauer Emmett Teller (BET) surface area analyzer.

membrane-science-Schematic-diagram

Figure 1: Schematic diagram of the CVD and experimental set-up.

Adsorption studies of chromium (VI) ion onto CNTs with best properties: The chromium (VI) adsorption experiments from its aqueous solutions on the prepared CNTs with best morphological properties were carried out using standard 10 mg/L, 50 mg/L and 100 mg/L Cr (VI) ion solution. The adsorption experiments were carried out by adding 0.2 to 1.0 g of the prepared CNTs adsorbents at an interval of 0.2 in 100 mL of the Cr (VI) ion solution. The optimal adsorption parameters are determined as a function of adsorbent dosage, pH, contact time and temperature in the batch removal process. The solution were kept in a water bath shaker at 200 rpm for a predetermined period of time, then after the solution was filtered using filter paper and Cr (VI) ion concentration in the filtrate was determined by an Atomic adsorption Spectrometer (PerkinElmer Analyst 400, Perkin–Elmer). The adsorption capacity and the percentage removal of Cr (VI) ion were calculated using Equation (1) and (2) respectively.

image

image

Where qe is the equilibrium adsorption capacity of the adsorbent (mg/g), Co and Ce is the initial and equilibrium concentration of Cr (VI) ion in solution (mg/L) respectively, m is the weight of the adsorbent (g) and V is the volume of the solution used (L).

Effect of CNTs Dosage on the percentage removal of chromium (VI) ion: The effect of adsorbent dosage on the adsorption of Cr (VI) ion solution with initial concentration of 10 mg/L, 50 mg/L and 100 mg/L prepared by different dilution of the stock solution (1000 mg/L). The solutions were contacted with different CNTs adsorbent dosage of 0.2, 0.4, 0.6, 0.8 and 1.0 g and sharked at 200 rpm at 30°C. The adsorbent was then filtered and the filtrate was then analyzed using the AAS. The optimum dosage is obtained where the percentage removal of the Cr (VI) ion is maximum from the experiments.

Effect of pH on the percentage removal of chromium (VI) ion: The effect of pH on the adsorption was studied by varying pH in a range of 2, 4, 6, 8, 10 and 12 at optimum CNTs do, contact speed of 200 rpm and room temperature. The pH of the solutions was adjusted sage in above section by drops of 0.5 mol/dm3 NaOH or 0.5 mol/dm3 HCl solutions. The pH meter was standardized with buffer solution before every measurement during the experiments.

Effect of contact time on the percentage removal of chromium (VI) ion: The effect of contact time on the adsorption was studied at an interval of 30, 45, 60, 75 and 90 minutess of Cr (VI) ion solution of initial concentration of 10 mg/L, 50 mg/L and 100 mg/L containing optimum CNTs dosage at room temperature and stirring speed of 200 rpm.

Effect of temperature on the percentage removal of chromium (VI) ion: The effect of temperature on the adsorption was studied at different temperatures of 30°C, 40°C, 50°C, 60°C and 70°C by taking optimum CNTs dosage at stirring speed of 200 rpm.

Results and Discussion

Kinetic studies

The kinetic of CNTs synthesis is hypothesized to be as follow. First is the decomposition of C2H2 to form free radicals in an inert environment on Fe-Ni/kaolin catalyst surface using argon as a carrier gas. Once the catalyst was exhausted, the CNTs formation occurred in the gas phase. As the residence time increases, the concentration of the active species changed, leading to a variability of the thickness of the CNTs. In this study, a simple growth kinetics model is applied to describe the observed CNTs growth as presented in the following proposed reactions mechanism.

Adsorption: C2H2 (g) + X → C2H2.X …… (3)

Surface reaction: C2H2. X → 2CNTs. X + 2H.X …… (4)

Desorption: CNTs. X → CNTs + X …… (5)

Desorption: 2H.X → H2 + 2X …… (6)

Equations (3) and (4) showed the adsorption and the surface reaction step respectively. While Equations (5) and (6) above, represented the CNTs growth with evolution of hydrogen gas. Assuming Langmuir Hinshelwood Equation [28], the kinetic expression for the rate of acetylene consumed denoted by “rC2H2”, from the proposed reaction mechanism can be written as;

image

Where kreaction is the kinetic parameter represents the constant of reaction rate, PC2H2 and PH2 are the partial pressures of the acetylene and hydrogen respectively. Presented in Table 1 were the experimental data’s used in the determination of kinetic parameters (kreaction, kC2H2 and kH2) using Equation (7) which can be linearized into Equation (8) for easy solving using POLYMATH 5.1 software

Reaction Temperature Partial pressure (atm) RC2H2
(°C) PC2H2 PH2 (mol/gcat. min)
700 0.0928 2.1351 0.0066
0.0846 1.9467 0.0055
0.0888 2.043 0.0061
750 0.0742 1.7061 0.0042
0.0762 1.7537 0.0045
0.0789 1.8153 0.0048
800 0.1289 2.9644 0.0128
0.1305 3.0012 0.0131
0.1153 2.6514 0.0102
850 0.0815 1.8748 0.0051
0.0828 1.9039 0.0053
0.0834 1.9183 0.0054
900 0.0322 0.7411 0.0008
0.0699 1.6066 0.0038
0.072 1.6571 0.004

Table 1: Gas-phase concentration of acetylene and hydrogen in the CVD reactor.

image

Were,

image

image

image

image

The estimation data of kinetics parameters were computed and the results are presented in Table 2. The activation energy E (J/mol) and the frequency factor A (per second) were determine by plotting in (Kreaction) against 1/T base on the Arrhenius equation (13) [29].

T (°C) kreaction KC2H2 KH2
700 8.93E-05 9.7194241 1.455795
750 0.00029213 10.263342 1.417312
800 0.00181886 5.028676 0.543685
850 0.00815072 2.0871586 0.158471
900 0.00835337 7.6981468 0.516337

Table 2: The estimation data of kinetics parameters.

image

Taking the natural logarithm of both sides in Equation (13), we have Equation (14)

image

Where Kreaction is the reaction rate constant, R is the gas constant (8.314 J/mol) and T is the absolute temperature (K).

Figure 2 revealed a strong fitting of the Langmuir Hinshelwood equation to the kinetic data with R2 value of 0.9569. Also, the value of the activation energy was obtained to be 237.2483 kJ/mol, which implies that the proposed mechanism by adsorption process is correct (i.e. acetylene bonds are broken down for the formation of new molecules of CNTs). In addition, the frequency factor (A) was obtained to be 5.0396 × 108/min which showed that the reactant species collide at faster rate for the formation of the CNTs. Substituting the values for Kreaction, KC2H2 and KH2 from Table 2 into Equation 7 for the prediction of the rate of decomposition of the acetylene at 700°C, 750°C, 800°C, 850°C and 900°C. Equations (15-19) are the formulated model from the Langmuir Hinshelwood model for predicting rate of decomposition of the acetylene at different reaction temperature.

membrane-science-activation-energy

Figure 2: Arrhenius plot for the determination of activation energy (E) and frequency factor (A).

Rate of decomposition of the acetylene at 700°C

image

image

Rate of decomposition of the acetylene at 750°C

image

Rate of decomposition of the acetylene at 800°C

image

Rate of decomposition of the acetylene at 850°C

image

Rate of decomposition of the acetylene at 900°C

image

image

Characterization of the prepared CNTs at different temperature

The prepared materials collected from the CVD reactor at different reaction temperature (700°C, 750°C, 800°C, 850°C and 900°C) were analyzed using scanning electron microscope (SEM), selected area electron diffraction (SAED) pattern, transmission electron microscope (TEM) and energy dispersive spectroscopy (EDS) in order to confirm that the deposited carbons are CNTs. The SEM images in Figures 3a-7a revealed formation of nanotubes at all the reaction temperatures. The SEM results also indicate decreased in the tubes diameters with increase in temperature from 700 to 900s and the radial distribution gets narrower at 900°C with better structural quality. The variation in structural quality as the temperature increases can be attributed to the fact that, at 700°C the catalyst was deactivated before all metal particles (Fe-Ni) were completely reduced therefore, loss of catalytic activity occurred which resulted in an incomplete decomposition of C2H2 gas, while the better structural quality observed at 900°C indicate complete decomposition of the C2H2 gas.

Furthermore, the SAED patterns in Figures 3b-7b exhibits a strong rings with a strong spots for (002), together with a ring for (110) and a pair of weak rings for (111) and (211) diffractions. There are diffuse haloes due to the amorphous carbon film on the copper grid and sharp rings due to the CNT. The reciprocal lattice spacing (1/d) of 3.0, 4.2, 5.2 and 7.2 nm−1 measured from the rings occurrences in Figures 3b-7b were used to determine the interplanar distance (d). The interplanar spacing values are calculated from Bragg’s diffraction equation using the diffraction ring diameter and the camera length of the transmission electron microscope (TEM). The calculated results presented in Table 3 indicate the interlayer spacing in the walls, about 0.33 nm, corresponds to (002) distance of graphite carbon which are in good agreement with those in literature for graphite. The SAED patterns in Figures 3b-7b for all the samples at various conditions gave very consistent result as expected (i.e. ring distance). This is because, the appearance of (002) plane diffractions as a pair of rings indicates orientation of the (002) planes in the CNTs for all the samples.

membrane-science-SAED-pattern

Figure 3: (a) SEM image (b) SAED pattern (c) TEM image (d) EDS of CNTs at 700°C.

Graphite h, k, l dhkl(nm) 1/dhkl   (nm-1)
0, 0, 2** 0.3333 3
1, 1, 0* 0.2381 4.2
1, 1, 1 0.1923 5.2
2, 1, 1 0.1389 7.2

The first and second most strongly scattering lattice planes are respectively denoted ** and *

Table 3: Strongly scattering lattice planes in graphite.

More so, the TEM images in Figures 3c-7c revealed the formation of wall structures of CNTs with an encapsulated metal nanoparticles along the inside diameter of the nanotubes samples which resulted from the metal catalyst. The TEM images in Figure 3c-7c also indicate the multiple walls and concentric tubes with diameters less than 100 nm Figures 4-7. Whereas the EDS showed that the carbon contents increased from 84.91 wt.% to 95.29 wt.% with increase in temperature from 700°C to 900°C.

membrane-science-TEM-image

Figure 4: (a) SEM image (b) SAED pattern (c) TEM image (d) EDS of CNTs at 750°C.

membrane-science-SEM-image

Figure 5: (a) SEM image (b) SAED pattern (c) TEM image (d) EDS of CNTs at 800°C.

membrane-science-EDS-CNTs

Figure 6: (a) SEM image (b) SAED pattern (c) TEM image (d) EDS of CNTs at 850°C.

membrane-science-SAED-pattern

Figure 7: (a) SEM image (b) SAED pattern (c) TEM image (d) EDS of CNTs at 900°C.

In addition, the BET surface area was used to characterize the prepared CNTs and the results are presented in Table 4. Table 4 shows that the prepared CNTs have high surface areas as results of their nanoscale sizes. The BET surface area decreases from 534.45 m2/g to 379.44 m2/g at a temperature of 700°C and 750°C respectively. At 800°C reaction temperature, CNTs with highest BET surface area of 567.10 m2/g was formed. But above 800°C, the surface area decreases.

Reaction Temperature BET Surface Area (m2/g)
700 534.45
750 379.44
800 567.1
850 472.98
900 388.05

Table 4: BET surface area of CNTs prepared at different reaction temperature.

It can be observed in Table 4 that CNTs prepared at reaction temperature of 800°C gives the highest BET surface area of 567.10 m2/g than that of the CNTs prepared at 700°C, 750°C, 850°C and 900°C. This surface area can be considered well enough for an adsorption process to take place.

Adsorption studies of chromium (VI) ion onto the prepared CNTs at 800°C

More previously mention, CNTs prepared at 800°C give the highest BET surface area than when compared with others prepared at 700°C, 750°C, 850°C and 900°C. Therefore, the CNTs at 800°C are used as an adsorbent in the adsorption study of chromium (VI) ion.

Effect of CNTs Dosage on the percentage removal of chromium (VI) ion: The resulted presented in Figure 8 show the effect of CNTs dosage on the removal of Cr (VI) ion at a pH of 7 in room temperature and contact time of 45 min with initial Cr (VI) concentration of 10 mg/L, 50 mg/L and 100 mg/L. The figure revealed that the removal of Cr (VI) ion increases from 89.8 % to 99.3, 88.5 % to 97.15 % and 87.0 % to 96.9 % for the initial Cr (VI) ion concentration of 10 mg/L, 50 mg/L and 100 mg/L respectively as the adsorbent dosage increases. It is observed that after 0.8 g of mass of the CNTs adsorbent, there is no significant change in the percentage removal of Cr (VI) and this may be due to the overlapping of active sites at high CNTs dosage which reduces the effective surface area because of the conglomeration of the particles exchange. Therefore, 0.8 g/ 100 mL is considered as the optimum CNTs dosage which is used for further studies.

membrane-science-percentage-removal

Figure 8: Effect of CNTs Dosage on the percentage removal of chromium (VI) ion.

Effect of pH on the percentage removal of chromium (VI) ion: The results in Figure 9 show the effect of pH on percentage removal of Cr (VI) at different pH using 0.8 g of CNTs in chromium solution by keeping other parameters constant. These results revealed that, there is an increase in percentage removal of Cr (VI) with increase in pH until 8. After a pH of 8, it was observed that the percentage removal of the ions started to decrease and this confirmed that Cr (VI) ion removal is favorable at alkalinity medium. Similar results are reported in chromium removal by aluminum magnesium mixed with hydroxide [30].

membrane-science-removal-chromium

Figure 9: Effect of pH on the percentage removal of chromium (VI) ion.

Effect of contact time on the percentage removal of chromium (VI) ion: The results of the effect of contact time on the percentage removal of Cr (VI) for initial concentration of 10 mg/L, 50 mg/L and 100 mg/L at optimum CNTs dosage and pH of 7 is presented in Figure 10. It cleared from the figure that equilibrium is reached after 45 min for initial Cr (VI) ion concentration of 10 mg/L and 60 min for initial Cr (VI) concentration of 50 mg/L and 100 mg/L. This observable trend may be due to the fact that the total vacant sites in the prepared CNTs initially and the solute concentration gradient were very high. As the time increases, the Cr (VI) ion uptake rate by the CNTs decreases due to decrease in the number of active adsorption sites as well as Cr (VI) ion concentration. Similar results have been reported by many researchers.

membrane-science-contact-time

Figure 10: Effect of contact time on the percentage removal of chromium (VI) ion.

Effect of temperature on the percentage removal of chromium (VI) ion: The results of the effect of temperature on the percentage removal of Cr (VI) ion for initial concentration of 10 mg/L, 50 mg/L and 100 mg/L at optimum CNTs dosage and pH of 7 is presented in Figure 11. The figure revealed that increase in temperature from 30°C to 45°C increases the percentage removal of Cr (VI) ion from 94% to 99.51%, 95% to 99.3% and 98.2% to 99.3% for initial Cr (VI) ion concentration of 10 mg/L, 50 mg/L and 100 mg/L respectively which shows the endothermic nature of the adsorption process and this may be probably due to the decrease in the escaping tendency of the adsorbate species from the surface of the CNTs adsorbent. Similar findings have been reported by Rengaraj et al. [31], which study the removal of chromium in wastewater using ion exchange resins.

membrane-science-Effect-temperature

Figure 11: Effect of temperature on the percentage removal of chromium (VI) ion.

Kinetic studies of chromium (VI) ion onto the prepared CNTs at 800°C

In order to understand the efficiency of the adsorption process of the chromium (VI) ion onto the prepared CNTs, the pseudo first order (Lagergren rate equation) and second order rate equations are applied to model the kinetic of Cr (VI) ion adsorption onto the CNTs. Figure 12 shows a straight lines plots of Log (qe-qt) against time (t) for initial Cr (VI) ion concentration of 10 mg/L, 50 mg/L and 100 mg/L while the plots of linearized second order rate equation for initial Cr (VI) ion concentration of 10 mg/L, 50 mg/L and 100 mg/L were shown in Figure 13.

membrane-science-first-order-reaction

Figure 12: Pseudo first order reaction of chromium (VI) ion adsorbed onto CNTs.

membrane-science-order-reaction

Figure 13: Pseudo second order reaction of chromium (VI) ion adsorbed onto CNTs.

The pseudo first and second order rate equation constants from Figures 12 and 13 for initial Cr (VI) ion concentration of 10 mg/L, 50 mg/L and 100 mg/L were determined and the results are presented in Table 5 along with the corresponding correlation coefficients. Table 5 reveal that the coefficient of determination (R2) for second order rate equation is less than that of first order rate equation, which suggested that the adsorption process in this experimental study followed the first order Lagergren’s kinetic.

Initial Cr (VI)  ion Conc. Pseudo First Order Rate Equation Second Order Rate Equation
(mg/L) K1 qe R2 K2 qe R2
  (min-1) (mg/g) (g mg-1min-1) (mg/g)
10 0.0196 1.1223 0.9877 0.002 15.4083 0.9677
50 0.0302 2.7585 0.9826 0.0017 16.5837 0.9154
100 0.0177 2.4973 0.8925 0.0014 19.3424 0.7646

Table 5: Pseudo first and second order rate equations constants.

Isotherm studies of chromium (VI) ion onto the prepared CNTs at 800°C

The linear plots of the Langmuir, Freundlich, Dubinin- Radushkevich and Temkin isotherm models for the adsorption of Cr (VI) ion onto the prepared CNTs are presented in Figures 14-17 respectively. The straight lines plots of the isotherms confirmed the satisfactory fits of the application of the Langmuir, Freundlich, Dubinin-Radushkevich and Temkin isotherm models to the adsorption of Cr (VI) ion onto the CNTs adsorbent.

membrane-science-Adsorption-Isotherms

Figure 14: Langmuir Adsorption Isotherms.

membrane-science-Freundlich-Adsorption

Figure 15: Freundlich Adsorption Isotherms.

membrane-science-Dubinin-Radushkevich

Figure 16: Dubinin-Radushkevich Adsorption Isotherms.

membrane-science-Temkin-Adsorption

Figure 17: Temkin Adsorption isotherms.

Base on the graphical representation of the Langmuir, Freundlich, Dubinin-Radushkevich and Temkin isotherm models in the above figures, the isotherms constants values were computed and the results were presented in Table 6.

Langmuir isotherm constant
KL (L/mg) QO (mg/g) R2
0.001301 333.3333 0.9914
Freundlich isotherm constant
Kf (mg-1) n R2
0.642493 1.133016 0.9758
Dubinin-Radushkevich isotherm constant
K qm (g/g) R2
0.0001 40.0088 0.9092
Temkin isotherm constant
AT (L/g) β R2
0.06784 20.105 0.9355

Table 6: Summary of values for isotherms models of chromium (VI) ion onto CNTs.

From Table 6, the R2 value obtained for the Langmuir isotherm was 0.9914 indicating the applicability of the Langmuir adsorption isotherm, and the values of QO and KL were calculated to be 333.33 mg/g and 0.0013 L/mg respectively. Meanwhile, for the Freundlich isotherm, the R2 value obtained was 0.9758, KF and n were evaluated to be 0.6425 and 1.133 respectively. Also, the Dubinin Radushkevich R2 was found to be 0.9092 and the values of K and qm were calculated to be 0.0001 and 40.0088 respectively, while the R2, AT and β were calculated to be 0.9355, 0.06784 L/g and 20.105 respectively for the Temkin isotherm. It is clear that the Langmuir isotherm fits better than Freundlich, Dubinin Radushkevich and Temkin isotherm on the basis of correlation coefficient values and this implies that the Langmuir model is more appropriate to describe the adsorption characteristic of Cr (VI) ions onto CNTs adsorbent in this study.

The Langmuir, Freundlich, Dubinin Radushkevich and Temkin equations were developed to fit Cr (VI) ions equilibrium adsorption capacity, qe onto the CNTs adsorbent. The Equations (20-23) represent the developed Langmuir, Freundlich, Dubinin Radushkevich and Temkin equations for adsorption of Cr (VI) ions onto the CNTs adsorbent.

The developed Langmuir Equation;

image

The developed Freundlich Equation;

image

The developed Dubinin Radushkevich Equation;

image

The developed Temkin Equation;

image

Conclusions

In summary, CNTs was successfully synthesized using bimetallic catalyst (Fe-Ni) supported on kaolin via CVD method by measuring the activation and frequency factor of acetylene (C2H2) decomposition. The kinetic studies showed that the CVD reaction is controlled and described by the Langmuir Hinshelwood kinetic model. This study demonstrated the mechanism and growth kinetics of CNTs by CVD method using acetylene gas as carbon source and Fe-Ni catalyst over kaolin substrate in an inert environment. CNTs synthesized at 800°C was observed to be the most highly quality nanotubes containing fewer defects and it was used for adsorption study. The adsorption experiments revealed good capability of the prepared CNTs in removal of chromium (VI) ion at an optimum dosage of 0.8 g/100 mL, pH of 8; 45 minutes contact time and temperature of 45°C. The kinetic adsorption parameters showed that the overall adsorption can be better described by the pseudo first order kinetic model, while the equilibrium data were best fitted by the Langmuir isotherm in the adsorption of Cr (VI) ion onto the prepared CNTs.

References

  1. Karim I, Abdulkareem AS, Aliyu A, Garba MU, Mohammed A. Optimization of lead (II) ions adsorption on to chemically activated carbon from sugarcane bagasse. Nigeria J Technol Research. 2015;10(2): 27-33.
  2. Krawczyk M, Jeszka-Skowron M. Multiwalled carbon nanotubes as solid sorbent in dispersive micro solid-phase extraction for the sequential determination of cadmium and lead in water samples. Microchem J. 2016;126: 296-301.
  3. Wang F, Lu X, Lia XY. Selective removals of heavy metals (Pb2+, Cu2+ and Cd2+) from wastewater by gelation with alginate for effective metal recovery. J Hazard Mater. 2016;308: 75-83.
  4. Stafiej A, Pyrzynska K. Adsorption of heavy metal ions with carbon nanotubes. Sep Purif Technol. 2007;58(1): 49-52.
  5. Goyer RA (1996) Toxic effects of metals. In Casarett and Doull’s toxicology: The basic science of poisons’’. Toxicology 44: 121-122.
  6. Tahir SS, Naseem R. Removal of Cr (III) from tannery wastewater by adsorption onto bentonite clay. Sep Purif Technol. 2007;53(3): 312-321.
  7. Sacmac S, Kartal S, Yilmaz Y, Sacmac M, Soykan C. A new chelating resin: Synthesis, characterization and application for speciation of chromium (III)/(VI) species. Chemical Engineering J. 2012;181-182: 746-753.
  8. Saad MA, El-Rayis OA, Ahdy HH. Status of nutrients in Lake Mariut, a delta lake in Egypt suffering from intensive pollution. J Environ Biol. 1984;15(11):408-411.
  9. Guo Z, Zhu J, Wei S, Ho T. Magnetic nanocomposites for environmental remediation. Advanced Powder Technology. 2013;24:459-467.
  10. Jung C, Heo J, Han J, Her N, Lee SJ, Oh J, et al. Hexavalent chromium removal by various adsorbents: Powdered activated carbon, chitosan, and single/multi-walled carbon nanotubes. Sep Purif Technol. 2013;106: 63-71.
  11. Panayotova M. Kinetics and thermodynamics of copper ions removal from wastewater by use of zeolite. Waste Manag. 2001;21(7): 671-676.
  12. Turker AR. New sorbents for solid-phase extraction for metal enrichment. Clean. 2007;35(6): 548-557.
  13. Iijima S. Helical microtubules of graphitic carbon. Nature. 1991;354: 56-58.
  14. Gamaly EG, Ebbesen TW. Mechanism of carbon nanotube formation in the arc discharge. Phys Rev B. 1995;52(3):2083-2089.
  15. Height MJ, Howard JB, Tester JW, Vander Sande JB. Flame synthesis of single-walled carbon nanotubes. Carbon. 2004;42(11): 2295-2307.
  16. Yuan L, Saito K, Pan C, Williams FA, Gordon AS. Nanotubes from methane flames. Chem Phys Lett. 2001;340(3-4): 237-241.
  17. Aliyu A, Abdulkareem AS, Kovo AS, Abubakre OK, Tijani JO, Kariim I. Synthesize multi-walled carbon nanotubes via catalytic chemical vapour deposition method on Fe-Ni bimetallic catalyst supported on kaolin. Carbon Lett. 2017;21: 33-50.
  18. Mohammed IH, Bankole MT, Abdulkareem AS, Ochigbo SS, Afolabi AS, Abubakre OK. Full Factorial Design Approach to Carbon nanotubes synthesis by CVD method in Argon environment. South African Journal of Chemical Engineering. 2017;24: 17-42.
  19. Voelskow K, Becker MJ, Xia W, Muhler M, Turek T. The influence of kinetics, mass transfer and catalyst deactivation on the growth rate of multiwalled carbon nanotubes from ethane on a cobalt-based catalyst. Chem Eng J. 2014;244: 68-74.
  20. Wan H, Delale F, Shen L. Effect of carbon nanotube (CNT) content on the properties of in-situ synthesis CNT reinforced Al composites.  Mech Res Commun. 2016;660(5): 11-18.
  21. Andrews R, Jacques D, Rao AM, Derbyshire F, Qian D, Fan X, et al. Continuous production of aligned carbon nanotubes: a step closer to commercial realization. Chem Phys Lett. 1999;303(5-6): 467-474 (1999).
  22. Aliyu A, Kariim I, Abdulkareem AS. Effects of aspect ratio of Multi-walled carbon nanotubes on coal washery waste water treatment. J Environ Manage. 2017;202(1): 84-93.
  23. Abdulrahaman MA, Abubakre OK, Abdulkareem SA, Tijani JO, Aliyu A, Afolabi AS. Effect of coating mid steel with CNTs on its mechanical properties and corrosion behaviour in acidic medium. Adv Nat Sci Nanosci Nanotechnol. 2017;8: 015016.
  24. Kim H, Saiz E, Chhowalla M, Mattevi C. Modeling of the self-limited growth in catalytic chemical vapor deposition of graphene. New J. Phys. 2013;15: 053012.
  25. McCarty KF, Feibelman PJ, Loginova E, Bartelt NC. Kinetics and thermodynamics of carbon segregation and graphene growth on Ru (0001). Carbon. 2009;47:1806-1813.
  26. Losurdo M, Giangregorio MM, Capezzuto P, Bruno G. Graphene CVD growth on copper and nickel: role of hydrogen in kinetics and structure. Physical Chemistry Chemical Physics. 2011;13: 20836-20843.
  27. Bi H, Sun S, Huang F, Xie X, Jiang M. Direct growth of few-layer graphene films on SiO2 substrates and their photovoltaic applications. J Mater Chem. 2012;22(2): 411-416.
  28. Fogler HS (2010) Essentials of Chemical Reaction Engineering. Pearson Education 7.
  29. Wang W, Kunwar S, Huang JY, Wang DZ, Ren ZF. Low temperature solvothermal synthesis of multiwall carbon nanotubes. Nanotechnology. 2005;16(1): 21-23.
  30. Li QL, Zhang X, Yan Y (2009) Kinetic parameters and mechanisms of the batch biosorption of Cr (VI) and Cr (III) onto Leesia hexandra Swartz biomass. J colloid interface Sci 333: 71-77.
  31. Rengaraj S, Yeon KH, Moon SH. Removal of chromium from water and wastewater by ion exchange resins. J Hazardous Mater. 2001;87(1-3): 273-287.
Citation: Ahmed A, Abdulhakim SA, Ishaq K, Saka AA, Peter MS, Chidinma OU (2017) Carbon Nanotubes: Mechanism, Langmuir Hinshelwood Growth Kinetics and It Application for the Removal of Chromium (VI). J Membr Sci Technol 7: 174.

Copyright: © 2017 Ahmed A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
bellicon