Comparative Kinetic Study of Removal of Pb 2 + Ions and Cr 3 + Ions from Waste Water using Carbon Nanotubes Produced using Microwave Heating

A comparative study of the removal of Pb2+ ions and Cr3+ ions was conducted to determine the efficiency of carbon nanotubes (CNTs) produced using microwave heating as an adsorbent in removing heavy metal ions from waste water. Optimization of parameters such as adsorbent dosage, pH value, agitation speed, and agitation time was done using the Design Expert software version 6.0. The statistical analysis revealed that optimized conditions for the highest removal for Pb2+ are at pH 4.0, CNTs dosage of 0.09 g, agitation time and speed of 50 min and 150 rpm respectively. Meanwhile, the highest removal Cr3+ ions was observed at pH 8.0, CNTs dosage of 0.09 g, agitation time and speed of 60 min and 150 rpm respectively. For the initial concentration of 2 mg/L, the removal efficiency of Pb2+ ions and Cr3+ ions were 99.9% and 95.5% respectively. The maximum adsorption capacities of both Pb2+ ions and Cr3+ ions onto the CNT were 15.34 mg/g for Pb2+ ions and 24.45 mg/g for Cr3+ ions. Besides that, the Langmuir and Freundlich constants for the removal of Pb2+ ions were 0.073 and 1.438 L/mg while 0.071 and 1.317 L/mg for Cr3+ ions. The statistical analysis proved that the removal of Pb2+ ions and Cr3+ ions fits the Langmuir and Freundlich isotherm models, and both models obeyed the pseudo-second-order.


Introduction
New era industries have immensely improved the living standard of human beings.However, modern industries also caused serious adverse impacts on our surroundings.One of the major environmental concerns is water pollution by heavy metals.Heavy metals in water have been the main preoccupation for many years because of the toxicity towards aquatic-life, human beings and the environment [1].The United States Environment Protection Agency (USEPA) prepared a list called the Priority Pollutants List that identifies the organic and inorganic pollutants found in waste water which contribute the most to health hazards.The list includes antimony, arsenic, beryllium, cadmium, chromium, copper, lead, mercury, nickel, selenium, silver, thallium, and zinc [2][3][4][5][6].Even though some of the trace elements are essential in biological systems [7], heavy metal ions at high concentration are considered to be harmful and toxic to mankind, aquatic lives, and other living creatures of earth [8], because unlike organic pollutants, the majority is susceptible to biological degradation and heavy metal ions do not degrade into harmless end products.These heavy metal ions enter the water stream as waste water, discharged by various industries such as mining, alloy manufacturing, metal plating, galvanizing, smelting and paints.The main industries that contributes to heavy metal ion contaminations as a form of water pollution in Malaysia are the electroplating and fabrication industries [9].Lead has been known for its harmful impacts on the surrounding by accumulating readily into living systems.Its poison in human may cause serious illness like anaemia, kidney failure and nervous system damage, even fatal, as it accumulates mainly in bones, kidney, brain and muscles [10].In addition, the contamination of low lead level in children could result in behavior and learning problems, hyperactivity, low IQ, slow growth and also hearing problems [11].The cancer rate has also been increasing in the recent few years because of lead's presence in drinking and natural water [12].Meanwhile, Chromium is one of the extremely toxic heavy metals found in various industrial waste waters [13].The physiological effects of the ingestion of Cr 3+ ions on human health have also been studied intensively.Public health consideration of chromium is mostly related to Cr 3+ compounds that are irritants due to their high solubility and diffusivity in tissue, allowing them to cross biological membranes easily.It is documented that certain Cr 3+ compounds are carcinogenic and mutagenic.The toxic effects of Cr 3+ ions on humans include liver damage, internal hemorrhage, respiratory disorders, dermatitis, skin ulceration and chromosome aberrations [14].Various chemical removal methods have been utilized and further developed over decades to take charge of the heavy metal contaminations.The removal of heavy metal from aqueous solution consists of physical, chemical and biological techniques.Suggested conventional methods are electrochemical treatment, chemical precipitation, membrane technologies and adsorption on activated carbon [15][16][17].Among all the methods, adsorption on activated carbon is considered to be one of the method for removal heavy metals from aqueous solutions have been reported earlier [18].In addition, it is another good method to be taken into account from the aspect of handling methods and economics.Even though there are so many adsorbents available, researchers had to come up with a new adsorbent as the existing adsorbents were lacking in its efficiency to remove metal ions [19].
Since discovery of carbon nanotubes (CNTs) is a new member in the carbon family, found by Iijama [20].It is essentially a new type of adsorbents that proves to retain great potential for removal of pollutants such as herbicides and chloro-benzenes, as well as lead and chromium ions [21][22][23][24][25]. Researchers have found that CNTs have a relatively larger surface area, extraordinary surface morphology and good chemical and mechanical properties [26,27] that provide a good opportunity for the removal of heavy metals, [28][29][30].CNTs based technologies found its water-treatment applications in various fields, for instance as sorbents, catalyst, filters, or membranes [31].It is of common interest that the development of new technique for an efficient and selective synthesis of CNTs is at the cheapest possible cost.One of such possibilities is the use of microwave radiation.The reason behind the choice of microwave usage to produce CNTs is the novelty of this method [32].Microwave-assisted modification of carbon nanotube is non-invasive, simple, fast, environmental friendly and clean method as compared to traditional methods.Usually, the use of microwave facilitates and accelerates reactions, often improving relative yields [33,34].The use of microwave radiation in the synthesis and functionalization of CNTs or other nanostructures is advantageous because it provides a fast and uniform heating rate that can be selectively directed towards a targeted area compared to the conventional method usage.
The aim of this study, statistical optimization and comparative study on the removal of Pb 2+ metal ions and Cr 3+ metal ions from aqueous solution using CNTs produced using microwave heating was investigated.The operating parameters such as adsorbent dosage, pH value, agitation speed and time were exerted to study the effect of each parameter in the removal of heavy metal ions which are Pb 2+ metal ions and Cr 3+ metal ions in this case, using CNTs produced using microwave heating.Besides that, the kinetic and isotherm model equation for the removal of both Pb 2+ metal ions and Cr 3+ metal ions were also investigated to determine the optimum condition to obtain the maximum adsorption capacity of CNTs used in this study.

Characterization of Carbon Nanotubes (CNTs)
The CNTs were examined by the Field Emission Scanning Electron Microscopy (FESEM) and Transmission Electron Microscopy (TEM) as represented in Figure 1a-c respectively.As seen from the image, the diameter of the CNTs ranged from 10 to 20 nm with an average diameter of 15 nm, while the length was measured up to few microns.On the other hand, for the characterization on the structure of CNTs, the TEM was done.As observed from the images, the CNTs are tubular shaped with a hollow in it.Figure 1c is evident for the visibility of the catalyst particle inside the tubes.These CNTs are uniform in diameter distribution, have no deformation and are of high purity [35,36].

Characterization of Carbon Nanotubes (CNTs)
The CNTs were examined by the Field Emission Scanning Electron Microscopy (FESEM) and Transmission Electron Microscopy (TEM) as represented in Figure 1a-c respectively.As seen from the image, the diameter of the CNTs ranged from 10 to 20 nm with an average diameter of 15 nm, while the length was measured up to few microns.On the other hand, for the characterization on the structure of CNTs, the TEM was done.As observed from the images, the CNTs are tubular shaped with a hollow in it.Figure 1c is evident for the visibility of the catalyst particle inside the tubes.These CNTs are uniform in diameter distribution, have no deformation and are of high purity [35,36].Figure 2a-c shows the Fourier Transform spectra of the raw CNTs and the Pb 2+ and Cr 3+ heavy metal adsorption respectively.From the figure, it can be seen that the raw CNTs (a) demonstrates the insignificant lower peaks compared to the CNTs after the adsorption process as shown in Figure 2b,c.The CNTs after the adsorption process has three major peaks near 1200, 2400, 3450 cm −1 which are associated with groups (O-H), carbonyl groups (>C & O) and hydroxyl groups (-OH).This result acknowledges the results obtained in previous study [37][38][39][40][41].

Statistical Analysis of Adsorption of Pb 2+ and Cr 3+ onto CNTs
The Design Expert software version 6.0.8 was used to further investigate the statistical analysis of the adsorption of both Pb 2+ and Cr 3+ from the stock solutions prepared onto the CNTs.The most significant step in this study is the design of experiment which was obtained from the Design Expert.The design of experiment for the heavy metal adsorption of Pb 2+ and Cr 3+ done using the Design Figure 2a-c shows the Fourier Transform spectra of the raw CNTs and the Pb 2+ and Cr 3+ heavy metal adsorption respectively.From the figure, it can be seen that the raw CNTs (a) demonstrates the insignificant lower peaks compared to the CNTs after the adsorption process as shown in Figure 2b,c.The CNTs after the adsorption process has three major peaks near 1200, 2400, 3450 cm ´1 which are associated with groups (O-H), carbonyl groups (>C & O) and hydroxyl groups (-OH).This result acknowledges the results obtained in previous study [37][38][39][40][41].

Characterization of Carbon Nanotubes (CNTs)
The CNTs were examined by the Field Emission Scanning Electron Microscopy (FESEM) and Transmission Electron Microscopy (TEM) as represented in Figure 1a-c respectively.As seen from the image, the diameter of the CNTs ranged from 10 to 20 nm with an average diameter of 15 nm, while the length was measured up to few microns.On the other hand, for the characterization on the structure of CNTs, the TEM was done.As observed from the images, the CNTs are tubular shaped with a hollow in it.Figure 1c is evident for the visibility of the catalyst particle inside the tubes.These CNTs are uniform in diameter distribution, have no deformation and are of high purity [35,36].Figure 2a-c shows the Fourier Transform spectra of the raw CNTs and the Pb 2+ and Cr 3+ heavy metal adsorption respectively.From the figure, it can be seen that the raw CNTs (a) demonstrates the insignificant lower peaks compared to the CNTs after the adsorption process as shown in Figure 2b,c.The CNTs after the adsorption process has three major peaks near 1200, 2400, 3450 cm −1 which are associated with groups (O-H), carbonyl groups (>C & O) and hydroxyl groups (-OH).This result acknowledges the results obtained in previous study [37][38][39][40][41].

Statistical Analysis of Adsorption of Pb 2+ and Cr 3+ onto CNTs
The Design Expert software version 6.0.8 was used to further investigate the statistical analysis of the adsorption of both Pb 2+ and Cr 3+ from the stock solutions prepared onto the CNTs.The most significant step in this study is the design of experiment which was obtained from the Design Expert.

Statistical Analysis of Adsorption of Pb 2+ and Cr 3+ onto CNTs
The Design Expert software version 6.0.8 was used to further investigate the statistical analysis of the adsorption of both Pb 2+ and Cr 3+ from the stock solutions prepared onto the CNTs.The most significant step in this study is the design of experiment which was obtained from the Design Expert.The design of experiment for the heavy metal adsorption of Pb 2+ and Cr 3+ done using the Design Expert is shown in Tables 1 and 2 together with its effective removal percentage of Pb 2+ and Cr 3+ from the prepared stock solutions.The results obtained were utilized to further analyze the removal percentage of Pb 2+ and Cr 3+ from the prepared stock solutions with the usage of Design Expert that induces the optimum conditions for removal of both Pb 2+ and Cr 3+ from the prepared stock solutions.Attained optimized parameters and the successful removal percentage from Tables 1  and 2 were studied by the application of "Analysis of Variance" (ANOVA) from the Design Expert Software.Results from the ANOVA for the removal percentage of Pb 2+ and Cr 3+ from the prepared stock solutions are listed in Tables 3 and 4. Based on the results obtained from the ANOVA, the Fischer F-test value can be correlated to the mean square of the regressed model that leads to the comparison of the mean square of the residuals (errors).Efficiency of the model is validated as the F value increases.In contrast, the p value or lower probability indicates higher significance for the regression model.As seen from Table 3 for the adsorption Pb 2+ onto the CNTs, the value of 48.81 for F-test value indicates that the model is significant.On the other hand, the F-test value of 60.03 from Table 4 for the adsorption of Cr 3+ also proves that the model is significant.Meanwhile, the R-Squared and Adj R-Squared also hold an important function in determining the significance of the model.According to Tables 1 and 2 the values of R-Squared and Adj R-Squared for the adsorption Pb 2+ onto the CNTs are 0.9842 and 0.9640 respectively, while for the adsorption of Cr 3+ the values of R-Squared and Adj R-Squared are 0.9871 and 0.9706, respectively.This clearly shows that both values are quite close to each other, hence, indicating high significance and efficiency of the model.Evolved model equation for the removal of Pb 2+ (1) and Cr 3+ (2) from the prepared stock solutions is stated below; Removal % of Pb 2+ " 96.20 ´1.16A `1.22B `1.87C `0.53D ´0.44AB `0.088AC ´0.12AD ´1.37BC ´0.46BD ´0.44 CD Removal % of Cr 3+ " 6 8.41071429 `9.075A ´0.0361B `0.5416C `0.44D ´1.547AB 0.5461AC `1.403AD `0.14BC `0.99BD `0.68CD where, A represents the coded value of the pH of the prepared stock solution, B represents the coded value of the amount of adsorbent dosage, C represents the coded value of the agitation time or the contact time, and D represents the coded value of the agitation speed.In addition, the coefficient of single factor in the equation represents equation of the effect of that respective particular factor while the coefficients of double factors in the equation represent the effect and interaction between those two respective factors.Three-dimensional diagrams were plotted to observe the relationship between optimizing conditions and the Pb 2+ (Figure 3) and Cr 3+ (Figure 4) heavy metal ions removal percentage.As shown in Figures 3a and 4a, the correlation between adsorbent dosage and pH in the removal of Pb 2+ and Cr 3+ heavy metal ions indicates that both the removal percentages of the heavy metal ion increase when the adsorbent dosage is increased.This is because the increment of the adsorbent increases the availability of the surface area for the adsorption process, in which more of the heavy metal ions uptake onto the surface of the CNTs could occur [42][43][44].Based on Figures 3b and 4b which show the interaction between agitation time and the pH value in the removal of Pb 2+ and Cr 3+ heavy metal ions, they indicate the same pattern for both the heavy metal ions in which the removal percentage increases along with the agitation time allowed for the batch adsorption process.This is because longer contact time provides longer interaction duration between the heavy metal ions and adsorbent surfaces [45][46][47][48].Meanwhile, referring to Figures 3c and 4c which identify the interaction between agitation speed and pH value, they reflect different effects on both heavy metal ions.As in for Pb 2+ metal ions, the agitation speed does not have a significant effect on the removal percentage of Pb 2+ metal ions because the suspension may not become homogenous due to the rapid agitation, increasing the boundary layer between solid and liquid phase, hence lowering the removal percentage [49][50][51].On the other hand, for the Cr 3+ metal ions, as the agitation speed increases, the removal percentage increases owing to higher kinetic energy in which more molecules collide with each other increasing the adsorption capacity into the CNT binding sites, leading to higher removal percentages of Cr 3+ metal ions [52].Figure 5 shows the relationship between pH values and the removal percentages of both of the Pb 2+ and Cr 3+ heavy metal ions.As evident from the figure, the removal of Pb 2+ metal ions was favorable at lower pH because the alkaline state enhances metal precipitation, hence lowering the removal percentage.At the same time, removal of Cr 3+ metal ion was favorable at higher pH value because the acidic state increases the competition between Cr 3+ and H + in regards to the adsorption into the CNT.By increasing the pH value, the competition extinguishes as the OH ´ions increases.This proves that the removal of Cr 3+ metal ions works well in high pH value as it is more easily adsorbed into the CNTs surface [53,54].
C 2016, 2, 7 7 of 16 increasing the boundary layer between solid and liquid phase, hence lowering the removal percentage [49][50][51].On the other hand, for the Cr 3+ metal ions, as the agitation speed increases, the removal percentage increases owing to higher kinetic energy in which more molecules collide with each other increasing the adsorption capacity into the CNT binding sites, leading to higher removal percentages of Cr 3+ metal ions [52].Figure 5 shows the relationship between pH values and the removal percentages of both of the Pb 2+ and Cr 3+ heavy metal ions.As evident from the figure, the removal of Pb 2+ metal ions was favorable at lower pH because the alkaline state enhances metal precipitation, hence lowering the removal percentage.At the same time, removal of Cr 3+ metal ion was favorable at higher pH value because the acidic state increases the competition between Cr 3+ and H + in regards to the adsorption into the CNT.By increasing the pH value, the competition extinguishes as the OH − ions increases.This proves that the removal of Cr 3+ metal ions works well in high pH value as it is more easily adsorbed into the CNTs surface [53,54].The correlation of four parameters used in this research study for the removal of both Pb 2+ and Cr 3+ heavy metal ions are based on the analysis; it was found that the optimized conditions of parameter for the maximum removal of Pb 2+ as much as 99.9% could be attained with pH 4.0, agitation speed 150 rpm and the agitation time of 50, adsorbent dosage 0.09 g.As for Cr 3+ ion, the increasing the boundary layer between solid and liquid phase, hence lowering the removal percentage [49][50][51].On the other hand, for the Cr 3+ metal ions, as the agitation speed increases, the removal percentage increases owing to higher kinetic energy in which more molecules collide with each other increasing the adsorption capacity into the CNT binding sites, leading to higher removal percentages of Cr 3+ metal ions [52].Figure 5 shows the relationship between pH values and the removal percentages of both of the Pb 2+ and Cr 3+ heavy metal ions.As evident from the figure, the removal of Pb 2+ metal ions was favorable at lower pH because the alkaline state enhances metal precipitation, hence lowering the removal percentage.At the same time, removal of Cr 3+ metal ion was favorable at higher pH value because the acidic state increases the competition between Cr 3+ and H + in regards to the adsorption into the CNT.By increasing the pH value, the competition extinguishes as the OH − ions increases.This proves that the removal of Cr 3+ metal ions works well in high pH value as it is more easily adsorbed into the CNTs surface [53,54].The correlation of four parameters used in this research study for the removal of both Pb 2+ and Cr 3+ heavy metal ions are based on the analysis; it was found that the optimized conditions of parameter for the maximum removal of Pb 2+ as much as 99.9% could be attained with pH 4.0, agitation speed 150 rpm and the agitation time of 50, adsorbent dosage 0.09 g.As for Cr 3+ ion, the increasing the boundary layer between solid and liquid phase, hence lowering the removal percentage [49][50][51].On the other hand, for the Cr 3+ metal ions, as the agitation speed increases, the removal percentage increases owing to higher kinetic energy in which more molecules collide with each other increasing the adsorption capacity into the CNT binding sites, leading to higher removal percentages of Cr 3+ metal ions [52].Figure 5 shows the relationship between pH values and the removal percentages of both of the Pb 2+ and Cr 3+ heavy metal ions.As evident from the figure, the removal of Pb 2+ metal ions was favorable at lower pH because the alkaline state enhances metal precipitation, hence lowering the removal percentage.At the same time, removal of Cr 3+ metal ion was favorable at higher pH value because the acidic state increases the competition between Cr 3+ and H + in regards to the adsorption into the CNT.By increasing the pH value, the competition extinguishes as the OH − ions increases.This proves that the removal of Cr 3+ metal ions works well in high pH value as it is more easily adsorbed into the CNTs surface [53,54].The correlation of four parameters used in this research study for the removal of both Pb 2+ and Cr 3+ heavy metal ions are based on the analysis; it was found that the optimized conditions of parameter for the maximum removal of Pb 2+ as much as 99.9% could be attained with pH 4.0, agitation speed 150 rpm and the agitation time of 50, adsorbent dosage 0.09 g.As for Cr 3+ ion, the The correlation of four parameters used in this research study for the removal of both Pb 2+ and Cr 3+ heavy metal ions are based on the analysis; it was found that the optimized conditions of parameter for the maximum removal of Pb 2+ as much as 99.9% could be attained with pH 4.0, agitation speed 150 rpm and the agitation time of 50, adsorbent dosage 0.09 g.As for Cr 3+ ion, the optimized conditions for a maximum removal of 95.5% were found to be pH of alkaline state of 8.0, agitation speed 150 rpm and the agitation time of 60 with the maximum amount of dosage used which was 0.09 g.

Adsorption Kinetics and Adsorption Isotherm Studies
The kinetic study in this paper was conducted to identify the optimum time required for maximum adsorption of Pb 2+ metal ions and Cr 3+ metal ions into CNTs by altering the initial concentration of the solution at four different ranges of values.Based on the analysis done in Section 2.2, the best optimum conditions were determined to investigate the best contact time to denote the removal percentage.The amount of Pb 2+ and Cr 3+ metal ions adsorbed by both adsorbents, q t were obtained as shown is Figure 6a,b.The samples were collected at every 10 min time interval with a total contact time of 1 h for both heavy metal ions.The removal percentage of both Pb 2+ and Cr 3+ metal ion gradually increased and attained an almost perfect equilibrium level within the 1 h of agitation time.The pH value set for Pb 2+ metal ions stock solution was pH 4 while, the Cr 3+ metal ions stock solution was set to pH 8. optimized conditions for a maximum removal of 95.5% were found to be pH of alkaline state of 8.0, agitation speed 150 rpm and the agitation time of 60 with the maximum amount of dosage used which was 0.09 g.

Adsorption Kinetics and Adsorption Isotherm Studies
The kinetic study in this paper was conducted to identify the optimum time required for maximum adsorption of Pb 2+ metal ions and Cr 3+ metal ions into CNTs by altering the initial concentration of the solution at four different ranges of values.Based on the analysis done in Section 2.2, the best optimum conditions were determined to investigate the best contact time to denote the removal percentage.The amount of Pb 2+ and Cr 3+ metal ions adsorbed by both adsorbents, qt were obtained as shown is Figure 6a,b.The samples were collected at every 10 min time interval with a total contact time of 1 h for both heavy metal ions.The removal percentage of both Pb 2+ and Cr 3+ metal ion gradually increased and attained an almost perfect equilibrium level within the 1 h of agitation time.The pH value set for Pb 2+ metal ions stock solution was pH 4 while, the Cr 3+ metal ions stock solution was set to pH 8.In order to determine the adsorption isotherm and kinetic studies for this research, well known important isotherm models for instance Langmuir and Freundlich were employed.Both the isotherm models were tested to resolve the optimum model to determine the best model fit for the Pb 2+ metal ions and Cr 3+ metal ions adsorption into the Langmuir isotherm model which is capable of correlating the solid phase adsorbate concentration (qe) and the uptakes to the equilibrium liquid concentration (Ce) is as follows: In order to determine the adsorption isotherm and kinetic studies for this research, well known important isotherm models for instance Langmuir and Freundlich were employed.Both the isotherm models were tested to resolve the optimum model to determine the best model fit for the Pb 2+ metal ions and Cr 3+ metal ions adsorption into the Langmuir isotherm model which is capable of correlating the solid phase adsorbate concentration (q e ) and the uptakes to the equilibrium liquid concentration (C e ) is as follows: where, C e (mg/L) represents the unadsorbed heavy metal ions concentration at equilibrium, q e (mg/g) represents the amount of adsorbed heavy metal ions concentration per unit weigh of the adsorbent.Meanwhile, the affinity of binding sites established in the equation above is denoted as K L , and at the same time, q m is known as the maximum adsorption capacity, in which it indicates the limiting adsorption capacity of a particle when the active sites are fully occupied.Equation ( 4), which is the linearized form of the Langmuir Isotherm equation, was used to plot a graph of C e /q e against C e and the values of q m and K L were obtained respectively from the slope and interception of the graph.The adsorption isotherm for Langmuir model done for this study is represented in Figure 7a and it can be observed that the data retrieved satisfactorily fits the linearized equation for both heavy metal ions.The R 2 value obtained from the plot was 0.9941, and the values of q m and K L were calculated to be 15.34 and 0.078 mg/L.respectively for the Pb 2+ metal ions.Meanwhile for the Cr 3+ metal ions, the R 2 value obtained was 0.9846, calculated q m and K L were equals to 24.45 (mg/g) and 0.071 (L/mg) respectively.
C 2016, 2, 7 9 of 16 where, Ce (mg/L) represents the unadsorbed heavy metal ions concentration at equilibrium, qe (mg/g) represents the amount of adsorbed heavy metal ions concentration per unit weigh of the adsorbent.Meanwhile, the affinity of binding sites established in the equation above is denoted as KL, and at the same time, qm is known as the maximum adsorption capacity, in which it indicates the limiting adsorption capacity of a particle when the active sites are fully occupied.Equation ( 4), which is the linearized form of the Langmuir Isotherm equation, was used to plot a graph of Ce/qe against Ce and the values of qm and KL were obtained respectively from the slope and interception of the graph.The adsorption isotherm for Langmuir model done for this study is represented in Figure 7a and it can be observed that the data retrieved satisfactorily fits the linearized equation for both heavy metal ions.The R 2 value obtained from the plot was 0.9941, and the values of qm and KL were calculated to be 15.34 and 0.078 mg/L.respectively for the Pb 2+ metal ions.Meanwhile for the Cr 3+ metal ions, the R 2 value obtained was 0.9846, calculated qm and KL were equals to 24.45 (mg/g) and 0.071 (L/mg) respectively.Similarly, the adsorption isotherm for Pb 2+ metal ions and Cr 3+ metal ion were then plotted for another model which is the Freundlich model.The Freundlich model defines the interrelation between residual heavy metal ions equilibrium concentrations, Ce in mg/L with the heavy metal ions uptake capacities, qe (mg/g) of adsorbent.Equation ( 5) below indicates the Freundlich isotherm model that was used to plot the graph shown in Figure 7b.
ln qe = ln KF + ln Ce (5) where, KF is a Freundlich constant that represents the adsorption capacity of adsorbent and on the  Similarly, the adsorption isotherm for Pb 2+ metal ions and Cr 3+ metal ion were then plotted for another model which is the Freundlich model.The Freundlich model defines the interrelation between residual heavy metal ions equilibrium concentrations, C e in mg/L with the heavy metal ions uptake capacities, q e (mg/g) of adsorbent.Equation ( 5) below indicates the Freundlich isotherm model that was used to plot the graph shown in Figure 7b.ln q e " ln K F `1 n ln C e (5) where, K F is a Freundlich constant that represents the adsorption capacity of adsorbent and on the other hand, n is a constant that validates the intensity of relationship between the adsorbate and adsorbent.K F and n were both determined from the slope and interception of the linear plot of ln qe versus ln Ce.Based on the graph plotted, the values of n and K F were determined to be 1.438 and 1.34 L/mg respectively for the adsorption of Pb 2+ metal ions, whereby for the adsorption of Cr 3+ metal ions, n was figured to be 1.818 and the K F was evaluated to be 1.312 L/mg.In addition, by obtaining the R 2 value of 0.9946 for adsorption of Pb 2+ metal ions and 0.9925 for adsorption of Cr 3+ metal ions for the Freundlich plot, it indicates that the isotherm data fits well for the model.Table 5 shows the value determined for both Langmuir and Freundlich models.Review on removal of Pb 2+ and Cr 3+ as shown in Tables 6 and 7 respectively.The Langmuir and Freundlich equations were developed to fit both the Pb 2+ and Cr 3+ metal ions equilibrium adsorption capacity, q e and the concentration of unadsorbed metal ions and below equations were derived.The equations 6 and 7 represent the Langmuir and Freundlich equations for adsorption of Pb 2+ metal ions, while equations 8 and 9 represent the Langmuir and Freundlich equations for adsorption of Cr 3+ metal ions as shown below: Developed Langmuir Equation: q e " 1.121C e 1 `0.073C e (6) Developed Freundlich Equation : q e " 1.34C e ˝.6954 (7) Developed Langmuir Equation: q e " 1.7359C e 1 `0.071C e (8) Developed Freundlich Equation : q e " 1.818C e The pseudo-first-order kinetics and pseudo-second-order kinetics of Pb 2+ metal ions and Cr 3+ metal ions adsorption using CNTs were also investigated and the calculated kinetic adsorption values were further analyzed to estimate the sorption rates as well as to determine the suitable rate expressions characteristic of possible reaction mechanism.The pseudo-first-order and pseudo-second-order models employed for the data analysis are as shown below; ln pq e ´qt q " lnq e ´k1 t (10) where, q t represents the amount of heavy metal ions removed at time , while q e represents the adsorption capacity at equilibrium.The pseudo-first-order rate constant (L/min) is denoted as K 1 and t indicates the contact time (min).k 2 represents the rate constant of the pseudo second order adsorption (g/mg/min).The plotting of the graph log (q e ´qt ) versus time (t) for pseudo-first-order kinetic model did not yield in good convergence while in the pseudo-second-order adsorption, the equation 14 was applied to plot graph t/q t (min.g/mg)versus time (min) where all data converged well into a straight line with a high correlation coefficient R 2 .The values of slopes and intercepts obtained from the graph were tabulated in Table 8.As seen from Table 8, coefficients gained from the both the pseudo-first-order and pseudo-second-order models, it is evident that the pseudo-second-order-model fits the best.From Table 8, it is obvious that the R 2 values of the pseudo-second-order kinetic model are much higher than that of pseudo-first-order-kinetic-model and it experienced a consistent increase with the concentration compared to the values of the pseudo-first-order kinetic model [55].

Raw Material
Microwave assisted single stage production of Multiwall carbon nanotubes (MWCNTs) with a 16-23 nm outer diameter) and (98%) purity obtained from our previous work [32].

Preparation of Stock Solution
Analytical grade Pb 2+ and Cr 3+ standards which were obtained from Merck were used to prepare stock solutions containing 1000 mg/L of Pb 2+ and Cr 3+ metal ions which were further diluted using distilled water to attain the desired concentrations.In this research, the initial concentration of both Pb 2+ and Cr 3+ metal ions were both set to 2 mg/L and prepared stock solution was used to batch adsorption experiments.

Batch Adsorption
The batch adsorption experiment was conducted by treating the prepared stock solutions with different ranges of CNTs dosage from 0.03 to 0.09g, agitation speed from 100 to 150 rpm, pH of adsorption process from 4-6 for Pb 2+ and from 4-8 for Cr 3+ with varying agitation time from 10 to 50 min and from 10 to 60 min, respectively for Pb 2+ and Cr 3+ metal ions based on the design obtained from the Design of Expert software V6.0.8 arrangement (Perkin-Elmer, Waltham, MA, USA).The desired pH value of the stock solution was adjusted using 0.5 M of the NaOH solution.The Atomic Spectrometer (PerkinElmer Analyst 400, Perkin-Elmer) was employed to determine the initial and final concentrations of the Pb 2+ and Cr 3+ metal ions in order to calculate the amount of metal ion adsorbed by the CNTs.The detailed experiment design obtained from the Design Expert V6.0.8 for the removal of both the Pb 2+ and Cr 3+ metal ions were tabulated in Table 9a,b.Equations 12 and 13 below were used to calculate the metal ion adsorption capacities using the CNTs produced by microwave heating at a certain time designed, t and also to calculate the adsorption equilibrium of the metal ions.
q e " pC o ´Ce q V m where q t denotes the amount of metal ions adsorbed (mg/g) at given time, t and the q e indicates equilibrium concentration.C 0 , and C t denote the initial concentration of the metal solution, concentration metal ions at time t respectively, while Ce represents the equilibrium concentration of metal ions (mg/L) .V is the volume of metal ions stock solutions used (L) and m is the weight of the adsorbent dosage in grams (g).

Kinetic Study
The adsorption kinetics of Pb 2+ and Cr 3+ metal ions were carried out using four different concentrations for both Pb 2+ and Cr 3+ metal ions stock solution with the best optimizing parameters such as agitation speed and agitation time, and the adsorbent dosage of CNTs to be used was decided by the batch adsorption process and those conditions were employed for the adsorption kinetics study.The adsorption kinetic study for this research was done for an hour with 4 different concentrations of 30 mL of Pb 2+ and Cr 3+ metal ions stock solution whereby for every 10 min interval, a small amount, about 5 mL of the metal ions solution was withdrawn, filtered and checked for its concentration by using the Atomic Adsorption Spectrometer (AAS, Perkin-Elmer).The optimized parameters used to carry out the adsorption of Pb 2+ on the CNTs were adsorbent dosage of 0.06 g and agitation speed of 150 rpm, while for the adsorption of Cr 3+ were adsorbent dosage of 0.03 g and agitation speed of 125 rpm, gained from the Design Expert.The final concentrations of the stock solutions were again measured using the AAS.

Adsorption Isotherm
The adsorption Isotherm study for Pb 2+ and Cr 3+ metal ions were done by preparing four different concentrations of 5, 10, 15 and 20 mg/L of 30 mL of Pb 2+ and Cr 3+ metal ions stock solution.The best optimizing conditions were used to conduct this experiment in which the solutions were agitated for an hour with the agitation speed and adsorbent dosage of CNTs of 150 rpm and 30 mg respectively for both the Pb 2+ and Cr 3+ metal ions stock solutions prepared.The Atomic Adsorption Spectrometer was used to measure the final concentration of the solutions.Langmuir (14) and Freundlich Isotherm (15) models were applied to get the best model.

C e q e
" 1 K L q m `Ce q m (14) ln q e " ln K F `1 n ln C e (15) where q e : the adsorption density at the equilibrium solute concentration C e : (mg of adsorbate per g of adsorbent), C e : the equilibrium adsorbate concentration in solution (mg/L), q m : the maximum adsorption capacity corresponding to complete monolayer coverage (mg of solute adsorbed per g of adsorbent), and K L : the Langmuir constant related to energy of adsorption ( of adsorbent per mg of adsorbate), while K F and n are the empirical constants dependent on several environmental factors and is greater than one.

Conclusions
Based on all the analysis carried out for the obtained results, it is found that the Pb 2+ metal ions and Cr 3+ metal ions could be successfully removed from aqueous solution by using the CNTs.This proves that the CNTs serves as a good adsorbent in the removal of heavy metal ions, and it can be considered as a very convenient adsorbent to be used.The CNTs uses were characterized by using the Field Emission Scanning Electron Microscopy, Transmission Electron Microscopy and FT-IR.The effect of adsorption parameters such as the adsorbent dosage (CNTs) used, pH of stock solution, agitation speed, and agitation time for the heavy metal ion removal process were studied and optimized.The adsorption isotherm study was done by using the Langmuir and Freundlich Isotherm models while the kinetics studies on optimized conditions were done by employing the pseudo-first-order kinetics and pseudo-second-order kinetic modeling.Experimental results on the adsorption conditions showed that Pb 2+ have the highest adsorption capacity at a pH value of acidic state of 4.0, agitation speed 150 rpm and the agitation time of 50 with the maximum amount of dosage used which was 0.09 g.Meanwhile, the Cr 3+ has the highest adsorption capacity at a pH of alkaline state of 8.0, agitation speed 150 rpm and the agitation time of 60 with the maximum amount of dosage used which was 0.09 g.The Langmuir and Freundlich isotherm studies for Pb 2+ were calculated to be 0.9941 and 0.9948 respectively.On the other hand, the adsorption isotherm study for Cr 3+ results in R 2 of 0.9846 for the Langmuir model and 0.9925 for the Freundlich.The Langmuir and Freundlich constants for adsorptions of Pb 2+ metal ions show 0.078 and 1.38 L/mg respectively, and 24.45 and 1.312 L/mg for adsorption of Cr 3+ metal ions.
These values prove that both the isotherm models describe the adsorption process well.In addition, kinetics data obtained for both the Pb 2+ metal ions and Cr 3+ metal ions were best fitted by the pseudo-second-order model.Hence, the isotherm equilibrium on optimized condition was studied and the model equations were developed.

Figure 3 .
Figure 3.A 3D interaction plot of the removal of Cr 3+ using CNTs (a) interaction of adsorbent dosage and pH, (b) interaction of agitation time and pH and (c) interaction of agitation speed and pH.

Figure 4 .
Figure 4.A 3D interaction plot of the removal of Cr 3+ using CNTs (a) interaction of adsorbent dosage and pH, (b) interaction of agitation time and pH and (c) interaction of agitation speed and pH.

Figure 3 .
Figure 3.A 3D interaction plot of the removal of Cr 3+ using CNTs (a) interaction of adsorbent dosage and pH, (b) interaction of agitation time and pH and (c) interaction of agitation speed and pH.

Figure 3 .
Figure 3.A 3D interaction plot of the removal of Cr 3+ using CNTs (a) interaction of adsorbent dosage and pH, (b) interaction of agitation time and pH and (c) interaction of agitation speed and pH.

Figure 4 .
Figure 4.A 3D interaction plot of the removal of Cr 3+ using CNTs (a) interaction of adsorbent dosage and pH, (b) interaction of agitation time and pH and (c) interaction of agitation speed and pH.

Figure 4 .
Figure 4.A 3D interaction plot of the removal of Cr 3+ using CNTs (a) interaction of adsorbent dosage and pH, (b) interaction of agitation time and pH and (c) interaction of agitation speed and pH.

Figure 3 .
Figure 3.A 3D interaction plot of the removal of Cr 3+ using CNTs (a) interaction of adsorbent dosage and pH, (b) interaction of agitation time and pH and (c) interaction of agitation speed and pH.

Figure 4 .
Figure 4.A 3D interaction plot of the removal of Cr 3+ using CNTs (a) interaction of adsorbent dosage and pH, (b) interaction of agitation time and pH and (c) interaction of agitation speed and pH.

Table 1 .
Design of Experiment and removal percentage of Pb 2+ by CNTs.

Table 2 .
Design of experiment and removal percentage of Cr 3+ .

Table 3 .
Analysis of variance (ANOVA) for the removal percentage of Pb 2+ by CNTs.

Table 4 .
Analysis of variance (ANOVA) for the removal percentage of Cr 3+ by CNTs.

Table 5 .
Isotherm model for adsorption of Pb 2+ and Cr 3+ metal ions.

Table 6 .
Review on Langmuir and Freundlich isotherm parameter for Pb 2+ adsorption.

Table 7 .
Review on Langmuir and Freundlich isotherm parameter for Cr3+ adsorption.

Table 8 .
Pseudo-first-order and pseudo-second-order kinetics for adsorption of Pb 2+ and Cr 3+ metal ions.

Table 9 .
Optimizing conditions for batch adsorption of removal of (a) Pb 2+ and (b) Cr 3+ .