Adsorption of Pb2+ from Aqueous Solutions Using Novel Functionalized Corncobs via Atom Transfer Radical Polymerization.

The present study developed novel functionalized corncobs introducing brushes with dense and active carboxyl groups (-COOH), named MC-g-PAA, for the highly efficient adsorption of Pb2+ from aqueous solutions. MC-g-PAA were synthesized via atom transfer radical polymerization (ATRP) and characterized by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The amount of Pb2+ adsorbed on MC-g-PAA by hydrolysis with t-BuOK was 2.28 times greater than that with NaOH, attributed to the larger steric effect of t-BuOK, which reduced the hydrolysis of the bromo-ester groups. The influence of different parameters including the solid/liquid ratio, working solution pH, sorption temperature, and initial concentration and sorption time on the adsorption of Pb2+ were investigated in detail in batch experiments. Thermodynamic studies have shown that the adsorption process was spontaneous, endothermic, and accompanied by an increase in randomness. A better fit for the isotherm data was obtained using the Langmuir model than for the other four models and the maximum amount ( q max ) of Pb2+ adsorbed on MC-g-PAA was 342.47 mg/g, which is 21.11 times greater when compared with that of pristine corncobs (16.22 mg/g). The adsorption of Pb2+ on MC-g-PAA was very fast and followed the pseudo-second-order kinetic equation with a correlation coefficient of 0.99999. This monolayer adsorption process was dominated by chemical adsorption, and may proceed according to complexation and electrostatic interactions between Pb2+ and the carboxylate groups. This study indicated that MC-g-PAA could be successfully used as an adsorbent for the removal of Pb2+ from aqueous solutions due to its excellent efficiency.

1. Introduction

Traditional methods for the removal of Pb2+ from aqueous solutions such as chemical precipitation, ion exchange, oxidation, and membrane processes may be inefficient or extremely expensive, especially when the concentration of Pb2+ in solution is low, resulting in an environmental issue.

Adsorption is a more effective and widely adopted method for the removal of Pb2+ with low concentration. The adsorbent plays a very important role in the process of adsorption. Recently, many studies have focused on the utilization of agricultural waste in the removal of Pb2+ [1]. The potential of biosorption to replace conventional methods has been explored in previous studies because of its faster adsorption and lower cost [2]. However, the adsorption capacity of most biosorbents in nature is still low, which is an important reason for their slow development. To improve the adsorption capacity, researchers have chemically modified biosorbents by introducing active functional groups such as carboxyl [3,4].

Atom transfer radical polymerization (ATRP) is a controlled radical polymerization method that has been developed in recent years [5,6,7,8], and has been extensively investigated for grafting polymers onto substrates to increase active functional groups [4,9,10,11,12]. A great many modified adsorbents via ATRP such as functionalized cotton [9,10], aminated resin [11], triethylene-tetramine grafted magnetic chitosan [12], and poly (methacrylic acid)-grafted chitosan microspheres [4] have been investigated for their adsorption of different heavy metal ions. The results [4,9,10,11,12] showed that the adsorption capacities of these modified adsorbents were significantly improved due to introducing brushes with dense and active functional groups. Recent studies on carboxylate-functionalized adsorbents [4,7,13,14] have revealed that carboxylic groups (–COOH) have a strong adsorption affinity of metal ions, which can significantly improve the adsorption capacities of the adsorbent for metal ions. Therefore, it would be ideal if corncobs could be functionalized by introducing polymer brushes with dense and active carboxyl groups (–COOH).

Corncobs are agricultural by-products with no commercial value. Dried corncobs mainly consist of cellulose (38.4%) and hemicellulose (40.7%) [15]. It has been reported that some researchers investigated the removal of Cu2+, Zn2+, Pb2+, Ni2+, and Cd2+ from aqueous solutions using pristine and modified corncobs as biosorbents [15,16,17,18]. The results indicated that their adsorption capacity for metal ions increased when the corncobs were modified with citric acid, phosphoric acid [15], nitric acid [16] or sulfuric acid [17]. Tan et al. [18] also reported a 1.68-time increase in the adsorption capacity for Pb2+ of corncobs modified with CH3OH and NaOH (0.1 mol/L), where the adsorption capacity of modified corncobs could reach up to 43.41 mg/g.

In this study, novel functionalized corncobs introducing brushes with dense and active carboxyl groups (–COOH), named MC-g-PAA, were synthesized as adsorbents via atom transfer radical polymerization (ATRP) with the objective to investigate in detail the influence of different parameters including the solid/liquid ratio, working solution pH, sorption temperature, and the initial concentration and sorption time on the adsorption of Pb2+, which is a hazardous metal ion. Thermodynamics, isotherms, and kinetics were studied using their respective theoretical models to evaluate the effectiveness of MC-g-PAA for the adsorption of Pb2+ from aqueous solutions. The purpose of these studies was to elucidate the adsorption mechanisms. Furthermore, the novel functionalized corncob (MC-g-PAA) surfaces were characterized by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM).

2. Experimental

2.1. Reagents and Standards

2-bromoisobutyratebromide (BIBB, 98%), N,N,N,N,N-pentamethyldiethylenetriamine (PMDETA, 99%), potassium tert-butoxide (t-BuOK, 99%), 1,5-diazabicyclo [5.4.0] undec-5-ene (DBU, 98%), diisopropanolamine (DIPA, 98%), and lithium diisopropylamide (LDA, 98%) were purchased from Aldrich Chemical Company (Milwaukee, WI, USA). The standard Pb2+ stock solution (100 mg/L) was obtained from the National Chemical Reagent Company (Beijing, China) and diluted to the desired concentrations with deionized water. All other reagents for this study were procured from the Chinese Medicine Group Chemical Reagent Co. Ltd. (Shanghai, China) unless otherwise mentioned.

2.2. Preparation of the Corncobs

Corncobs were collected from the suburb of Xuzhou, China. These were thoroughly washed with deionized water, and dried at 333.15 K inside a convection oven for 24 h. Once the dried corncobs were cooled, they were crushed and sieved through a No. 50 mesh to obtain particles sized <0.3 mm. The ground corncobs were denoted as the GC.

About 50 g of GC was placed into a 1000 mL conical flask with a mixture of 250 mL ethanol and 250 mL NaOH solution (1 mol/L). The flask was shaken vigorously at a speed of 160 r/min for 1 h at 303.15 K to ensure that the extractive impurities were removed. After decantation and filtration, the treated corncobs (denoted as the TC) were washed with deionized water to remove the excess alkali and any other soluble impurities. The washing process was repeated until the pH value reached about 7.0. The TC were then dried at 333.15 K for 24 h inside a convection oven. This dried product was crushed and sieved through a No. 50 mesh.

2.3. Synthesis

2.3.1. Immobilization of ATRP Initiators on the Corncobs

As shown in Scheme 1, immobilization of the ATRP initiators on the corncobs was prepared as follows. First, 200 g of TC were transferred to 2 L reactor system (ChemRxnHub™, Chemglass Life Sciences, Vineland, FL, USA) with 1500 mL N-methyl-2-pyrrolidone (NMP). The mixture of 100 mL 2-bromoisobutyratebromide (BIBB) and 100 mL NMP was added dropwise into the reactor system using a constant pressure funnel in ice cold condition after 30 min of degassing with ultrapure nitrogen. Then, the reaction mixture was stirred continuously at a speed of 80 r/min for 24 h and left for 12 h at 333.15 K under an ultrapure nitrogen atmosphere. After the reaction, the products (containing the macroinitiator corncob-Br and denoted as the MC-Br) were washed with copious amount of ethanol. Finally, MC-Br was dried at 323.15 K inside a vacuum drying oven for 24 h. These dried products were crushed and sieved through a No. 50 mesh.

Scheme 1

Schematic representation for the synthesis of MC-g-PAA.

2.3.2. Grafting of Poly(Methyl Acrylate) on the Corncobs

MC-Br was used to start the polymerization of methyl acrylate (MA) via ATRP, where CuBr was used as the catalyst. First, 40 g of MC-Br was poured into the 2 L reactor system with 1000 mL MA. A total of 8 g CuBr and 12 mL PMDETA were added successively into the reactor systems after 10 min of continuous agitation. Then, the reactor system was degassed with ultrapure nitrogen for 30 min. The reaction mixture was stirred continuously at a speed of 80 r/min for 24 h and left for 24 h at 303.15 K under an ultrapure nitrogen atmosphere. After the reaction, the products (containing the poly(methyl acrylate) grafted corncobs and denoted as MC-g-PMA) were synthesized and washed with copious amount of methanol, acetone, tetrahydrofuran, ethanol, and deionized water, in that order [19]. Finally, MC-g-PMA was dried at 323.15 K inside a vacuum drying oven for 24 h. These dried products were crushed and sieved through a No. 50 mesh. The grafting yield was determined using the following equation: where (%) represents the grafting yield; (g) is the mass of the dry MC-Br before grafting; and (g) is the mass of the dry products after grafting.

2.3.3. Preparation of Functionalized Corncobs

The methyl acrylate of MC-g-PMA was turned into acrylic acid by hydrolysis, thus obtaining the poly(acrylic acid) grafted corncobs. About 2 g of MC-g-PMA was placed into a 100 mL conical flask with 50 mL of t-BuOK solution (0.4 mol/L). The flask was shaken vigorously in a thermostated shaker for 8 h at 160 r/min and 333.15 K. After decantation and filtration, the products (containing the poly(acrylic acid) grafted corncobs and denoted as MC-g-PAA) as the functionalized corncobs were washed with deionized water to remove excess t-BuOK and by-products of hydrolysis. The washing process was repeated until the pH value reached about 7.0. Finally, the MC-g-PAA was freeze-dried into a spongelike material inside a lyophilizer.

The hydrolysis yield was determined using the following equation: where (%) represents the hydrolysis yield; (g) is the mass of dry MC-g-PMA before hydrolysis; and (g) is the mass of the dry products after hydrolysis.

Various grades of MC-g-PMA were prepared by varying the alkalis (NaOH, t-BuOK, DBU, DIPA, LDA), concentrations of alkali (0.02–0.5 mol/L), hydrolysis times (0.5–12 h), and hydrolysis temperatures (303.15–353.15 K), and optimized the best conditions of preparation with respect to a higher amount of Pb2+ adsorbed.

2.4. Characterization

Functional groups were characterized by FTIR. The FTIR spectra of TC, MC-Br, MC-g-PMA, and MC-g-PAA were recorded on a FTIR spectrometer (Nicolet iS10, Thermo Fisher Scientific, Medison, WI, USA) using the KBr dispersion method. The KBr used in this study was of pure spectroscopic grade.

In order to analyze the morphological characteristics of GC, TC, MC-Br, MC-g-PMA, and MC-g-PAA, before and after adsorption of Pb2+, their images were obtained by a SEM (INSPECT S50, FEI Company, Hillsboro, OR, USA) at 10 kV accelerating voltage, at 2000× magnification.

2.5. Pb2+ Solutions

Pb2+ working solution (500 mg/L) was prepared by dissolving lead nitrate (7.99 g) in deionized water (10 L). Other desired solutions with lower concentrations of Pb2+ were obtained by proper dilutions of the working solution. The working solution pH was adjusted to the working value using a small amount of hydrochloric acid or sodium hydroxide. These solutions were prepared for the adsorption experiments.

2.6. Adsorption Experiments

Experiments were carried out by mixing dried adsorbents with the Pb2+ working solution. A total of 0.10 g of MC-g-PAA was transferred to a 100 mL conical flask with 75 mL of Pb2+ working solution (pH 5.0). The flask was shaken vigorously in a thermostated shaker for 2 h at 160 r/min and 303.15 K to ensure that the adsorption of Pb2+ approached the equilibrium. Flask contents were then removed and filtered to determine the residual Pb2+ concentration.

One parameter was varied at a time during optimization of the batch adsorption parameters for MC-g-PAA. The effect of the MC-g-PAA solid/liquid ratio was studied in the range of 0.005–0.25 g in 75 mL of working solution. The working solution pH was varied from 1.0 to 5.0. Adsorption thermodynamics was studied at various sorption temperatures in the range of 303.15–353.15 K. Adsorption isotherms were studied at various initial Pb2+ concentrations ranging from 50 to 500 mg/L with the MC-g-PAA dosage of 0.10 g/(200 mL). Adsorption kinetics was studied at various sorption times in the range of 0–180 min.

An analytical curve was made for calibration through the external standard method using standard Pb2+ solutions in a working range of 1–12 mg/L, which were obtained by proper dilutions of the standard Pb2+ stock solution (100 mg/L). The initial and equilibrium concentrations of Pb2+ were measured using the ContrAA 700 HR-CS AAS (Analytik Jena, Jena, Germany). All experiments were conducted three times and the mean values were presented in all cases. The removal efficiency for Pb2+ of MC-g-PAA was determined using the following equation [20]:

The amount of Pb2+ adsorbed on MC-g-PAA was calculated according to the following equation [20]: where (%) represents the removal efficiency for Pb2+ of MC-g-PAA at equilibrium; (mg/g) represents the amount of Pb2+ uptake per unit mass of the MC-g-PAA at equilibrium; and (mg/L) are the initial and equilibrium concentrations of Pb2+, respectively; (mL) is the volume of the working solution; and (g) is the dry mass of the MC-g-PAA.

3. Results and Discussion

3.1. Synthesis

The synthesis procedure of MC-g-PAA is illustrated in Scheme 1. In brief, the ground corncobs (GC) were first treated with ethanol and NaOH in order to hydrolyze esters and remove the extractive impurities. There were many reactive hydroxyl groups (–OH) on the treated corncobs (TC). Subsequently, these hydroxyl groups (–OH) and 2-bromoisobutyratebromide (BIBB) were reacted to produce the bromo-ester groups by condensation to provide alkyl bromide initiators (MC-Br). The polymerization reaction of MA via ATRP was then performed to immobilize poly(methyl acrylate) (PMA) brushes on the MC-Br (MC-g-PMA). Finally, the prepared MC-g-PMA were functionalized through hydrolysis with alkali in order to introduce high densities of carboxyl groups (–COOH) on the corncobs (MC-g-PAA).

The grafting yield was calculated as 778.35% using Equation (1). The higher the grafting yield, the more modified groups are produced. In order to obtain dense and active carboxyl groups (–COOH), it is expected that more methyl acrylate of MC-g-PMA is turned into acrylic acid by hydrolysis. However, the bromo-ester groups fabricated from the reaction of the hydroxyl groups on the corncobs with BIBB is possibly hydrolyzed in this process, resulting in the shedding of brushes with high densities of carboxyl groups onto the corncobs. Thus, to avoid this problem, the hydrolysis conditions were optimized.

Alkalis, the concentrations of alkali, hydrolysis times, and hydrolysis temperatures were investigated. NaOH, DBU, LDA, t-BuOK, and DIPA were tested (Figure 1), with a smaller amount of Pb2+ adsorbed on MC-g-PAA and a higher hydrolysis yield by hydrolysis with DBU, LDA, or DIPA, indicating that poly(methyl acrylate) (PMA) brushes of MC-g-PMA were rarely hydrolyzed and could not form many carboxyl groups (–COOH) on the corncobs. The amount of Pb2+ adsorbed on MC-g-PAA by hydrolysis with NaOH was 121.48 mg/g, but its hydrolysis yield was the lowest, suggesting that many poly(methyl acrylate) (PMA) brushes of MC-g-PMA were hydrolyzed, but most of the poly(acrylic acid) (PAA) brushes as hydrolyzates had come off. This is because the bromo-ester groups had also been hydrolyzed in the process. The amount of Pb2+ adsorbed on the MC-g-PAA by hydrolysis with t-BuOK reached its maximum of up to 277.51 mg/g, which is 2.28 times greater than that with NaOH, and attributed to its higher hydrolysis yield. The hydrolysis yield with t-BuOK was 30.9%, higher than that with NaOH because the larger steric effect of t-BuOK reduced the hydrolysis of the bromo-ester groups. Therefore, the best alkali to hydrolyze MC-g-PMA is t-BuOK.

Figure 1

Effect of alkalis on the adsorption of Pb2+ on MC-g-PAA and hydrolysis yield.

Similarly, as shown in Figure 2, Figure 3 and Figure 4, the maximum repeatable amount of Pb2+ adsorbed on MC-g-PAA was obtained using a concentration of 0.4 mol/L, a hydrolysis time of 8 h, and a hydrolysis temperature of 333.15 K.

Figure 2

Effect of t-BuOK concentration on the adsorption of Pb2+ on MC-g-PAA.

Figure 3

Effect of hydrolysis time on adsorption of Pb2+ on MC-g-PAA.

Figure 4

Effect of hydrolysis temperature on the adsorption of Pb2+ on MC-g-PAA.

3.2. Characterization

The FTIR spectra of TC, MC-Br, MC-g-PMA, and MC-g-PAA are shown in Figure 5. Peaks at 3417, 2904, 1640, 1378, and 1038 cm−1 were observed in the spectrum of TC. The broad and intense peak at 3417 cm−1 and the peak at 1378 cm−1 can be attributed to the O–H stretching and bending vibrations, respectively [18,21,22], which confirmed the presence of “free” hydroxyl groups on the TC. The peak at 2904 cm−1 is due to the C–H stretching vibration [18]. The peak observed at 1640 cm−1 was assigned to the C=O stretching vibration [18]. The presence of polysaccharide was manifested through a strong peak at 1038 cm−1 [18]. Compared to the spectrum of TC, there was a new peak at 1735 cm−1 in the spectrum of MC-Br, which can be attributed to the stretching vibration of C=O in the esters (the bromo-ester groups fabricated from the reaction of the hydroxyl groups on the corncobs with BIBB) [13,18,23,24,25]. This provides proof of successfully introducing the initiator groups on corncobs. In the spectrum of MC-g-PMA, the strong peaks that were evident at 1451 and 1735 cm−1 were due to the asymmetric deformation vibration of CH3 and the stretching vibration of C=O in the poly(methyl acrylate) [13,18,23,24,25], indicating that the dense PMA brushes were successfully grafted on the corncobs. In the spectrum of MC-g-PAA, the peaks at 1451 and 1735 cm−1 almost disappeared and a strong new peak at 1579 cm−1, due to the asymmetric stretching vibration of carboxyl groups in the poly(acrylic acid), can be observed [22,23], which indicates that the methyl acrylate of MC-g-PMA had been turned into acrylic acid by hydrolysis.

Figure 5

The FTIR spectra of TC, MC-Br, MC-g-PMA, and MC-g-PAA.

The surface morphologies of the functionalized corncobs at various stages were characterized by SEM. The SEM photographs of GC, TC, MC-Br, MC-g-PMA, and MC-g-PAA, before and after the adsorption of Pb2+ at 2000× magnification, are shown in Figure 6. It was observed that the surface of the GC was rough and uneven, and there were some cracks on the surface (Figure 6a). Due to the removal of some elements from GC by the mixture of ethanol and NaOH, TC had coarser and completely irregular surfaces as well as a plentiful variety of pores (Figure 6b). Some pores disappeared on the MC-Br surfaces (Figure 6c), which was due to the grafting of BIBB. This provides proof of successfully introducing the initiator groups on corncobs. The surfaces of the MC-g-PMA became smooth and some relatively close-grained polymers were clearly observed (Figure 6d), indicating that the dense PMA brushes were successfully grafted onto the corncobs. After the hydrolysis, the surfaces of the MC-g-PAA become coarse and have a good deal of variously sized pores owning to the removal of methyl groups and the shedding of some brushes with high densities of carboxyl groups from MC-g-PMA (Figure 6e). The SEM image of MC-g-PAA loaded with Pb2+ shows that some surfaces became uneven, but not rough, and that plenty of pores disappeared (Figure 6f), which indicates that Pb2+ in an aqueous solution is adsorbed on the MC-g-PAA. The introduction of brushes with high densities of carboxyl groups onto the corncobs can therefore be expected to change the surface properties and enhance the sorption of Pb2+.

Figure 6

SEM images of the GC: (a), TC (b), MC-Br (c), MC-g-PMA (d), MC-g-PAA (e), and MC-g-PAA loaded with Pb2+ (f).

3.3. Effect of Solid/Liquid Ratio

It is well known that the solid/liquid ratio greatly influences the removal efficiency for Pb2+ of MC-g-PAA [12,20]. The effect of the MC-g-PAA solid/liquid ratio was investigated between 0.005 and 0.25 g in 75 mL working solution and the results are shown in Figure 7.

Figure 7

Effect of the solid/liquid ratio on the adsorption of Pb2+ on MC-g-PAA.

Figure 7 shows that the removal efficiency for Pb2+ of MC-g-PAA was the lowest at minimum doses, and that it gradually increased as the adsorbent doses increased in the range from 0.005 to 0.20 g/(75 mL). Following this, it tended to be stable with further increases in adsorbent doses up to 0.25 g/(75 mL). Therefore, the maximum removal efficiency of Pb2+ was calculated as 99.5% at the solid/liquid ratio of 0.20 g/(75 mL). This can be attributed to the fact that at greater adsorbent doses, a more effective contact surface area is available for sorption.

3.4. Effect of Working Solution pH

It is well documented that the pH of the working solution plays an important role in adsorption of Pb2+ [12,13,20]. The Pb2+ working solution (500 mg/L) precipitates above pH 5.0, therefore, the influence of the initial pH was investigated at various pH values ranging from 1.0–5.0. The results are shown in Figure 8.

Figure 8

Effect of pH on the adsorption of Pb2+ on MC-g-PAA.

As indicated in Figure 8, a continuous increase in the adsorption capacity of Pb2+ on MC-g-PAA occurred in the range from 2.0 to 5.0. A small degree of sorption was observed below pH 2.0, while maximum adsorption took place at pH 5.0. Hence, the optimal pH, determined as 5.0, was used in further adsorption studies. Since Pb2+ and H+ compete for active sorption sites, the solution pH influences the sorption of Pb2+ on MC-g-PAA. At low pH, there is high concentration and high mobility of H+, which becomes adsorbed preferentially, resulting in relatively little sorption of Pb2+ on MC-g-PAA. As the working solution pH increases, the adsorption of Pb2+ also increases due to a smaller number of H+ and a greater number of negatively charged surface on MC-g-PAA.

3.5. Adsorption Thermodynamics

Thermodynamic parameters such as the free energy change (), enthalpy change (), and entropy change () can be estimated using thermodynamic equations [20,26]. The distribution coefficient (L/g) was determined by the following equation:

(kJ/mol) was calculated using the following equation:

(J/mol/K) and (kJ/mol) were calculated using the van’t Hoff equation by plotting a graph between and 1/T, where the slope gives the value of and the intercept represents . where (J/mol/K) represents the universal constant (8.314 J/mol/K) and (K) is the sorption temperature.

Thermodynamic studies have been undertaken by varying the sorption temperature from 303.15−353.15 K under optimized conditions. The results are shown in Figure 9 and Figure 10.

Figure 9

Effect of sorption temperature on the adsorption of Pb2+ on MC-g-PAA.

Figure 10

The van’t Hoff equation as against 1/T.

Figure 9 shows that the adsorption capacity of Pb2+ on MC-g-PAA increased slowly with an increase in the sorption temperature. Figure 10 shows a graphical representation of the van’t Hoff equation as against 1/T. The thermodynamic parameters for the adsorption of Pb2+ on MC-g-PAA were calculated using thermodynamic equations and Figure 10, and their values were recorded in Table 1.

Table 1

Thermodynamic parameters for adsorption of Pb2+ on MC-g-PAA.

T (K)	K_d(L/g)	ΔG^0(kJ/mol)	ΔS^0(J/mol/K)	ΔH^0(kJ/mol)
303.15	2.115	−1.888	15.86	2.926
313.15	2.197	−2.050
323.15	2.238	−2.164
333.15	2.352	−2.369
343.15	2.438	−2.543
353.15	2.476	−2.662

Table 1 shows that the values of were all negative, while the values of and were positive. Negative values of indicate that the adsorption of Pb2+ on MC-g-PAA was a spontaneous process, which is a common observation in most metal ion uptake processes. The value of was 2.926 kJ/mol, indicating that the adsorption of Pb2+ on MC-g-PAA was endothermic in nature. Furthermore, the adsorption capacity of Pb2+ increased as the sorption temperature increased, which was in good agreement with the experimental data from Figure 9. The value of was 15.86 J/mol/K, which indicated that the adsorption of Pb2+ on MC-g-PAA was accompanied by an increase in randomness.

3.6. Adsorption Isotherms

The main objective of the isotherm is to calculate the adsorption capacity of the adsorbent, which can also be used in gaining a better understanding of the mechanism of adsorption. Isotherm studies were performed using various initial concentrations of Pb2+, in the range of 50–500 mg/L, with the adsorbent dosage of 0.10 g/(200 mL). The connection between the amount of Pb2+ adsorbed at equilibrium and the equilibrium concentration of Pb2+ is shown in Figure 11.

Figure 11

Effect of equilibrium concentration on the adsorption of Pb2+ on MC-g-PAA.

From Figure 11, it is evident that the adsorption capacity of Pb2+ increased abruptly as the equilibrium concentrations of Pb2+ increased. Following this, the adsorption capacity increased slowly after the equilibrium concentration of 23.7 mg/L. At low initial concentrations of Pb2+, almost all of the Pb2+ was adsorbed due to plenty of vacant active carboxyl groups on the MC-g-PAA, resulting in relatively low equilibrium concentrations of Pb2+. As the initial concentrations of Pb2+ increased, the equilibrium concentrations of Pb2+ and the adsorption capacity of Pb2+ also increased because of the reduction in the vacant active carboxyl groups, indicating that MC-g-PAA approached the saturated state. In this study, experimental data were analyzed using the Langmuir, Freundlich, Temkin, Dubinin–Radushkevich, and Harkins–Jura isotherm models. The linearized Langmuir isotherm model can be expressed as [20,27]:

The dimensionless separation factor () of the Langmuir isotherm model is represented by [20,27]: where (mg/g) represents the maximum amount of Pb2+ adsorbed for monolayer formation on the adsorbent; (L/mg) is the Langmuir isotherm constant related to the adsorption energy; and (mg/L) is the initial concentrations of Pb2+. According to the values, the adsorption of Pb2+ from aqueous solutions using MC-g-PAA can be linear (= 1), unfavorable (> 1), favorable (0 << 1), and irreversible (= 0). The values of and were calculated from the slope and intercept of the linear plot between and .

The linearized Freundlich isotherm model is given by [20,28]: where (mg/g) and are constants of the Freundlich isotherm, which describe the adsorption capacity and intensity, respectively. The and values were evaluated from the slope and intercept of the linear plot between and .

The linearized Temkin isotherm model may be written as [29,30]: where (J/mol) and (L/mg) are constants of the Temkin isotherm. The values of and were calculated from the slope and intercept of the linear plot between and .

The linearized Dubinin–Radushkevich isotherm model is defined by [29,30]:

The adsorption free energy () was determined as follows: where (J/mol) is the adsorption potential energy and is the constant of the Dubinin–Radushkevich isotherm. The values of and were calculated from the slope and intercept of the linear plot between and .

The linearized Harkins–Jura isotherm model is given by [31]: where and are constants of the Harkins–Jura isotherm. The and values were evaluated from the slope and intercept of the linear plot between and .

Their correlation coefficients (R2) and the parameters of the five models are presented in Table 2. The linear plots of the Langmuir isotherm model is shown in Figure 12.

Table 2

Isotherm parameters for the adsorption of Pb2+ on MC-g-PAA.

Model	Parameter	Value
Langmuir	q_max (mg/g)	342.47
	K_L (min−1)	0.3023
	R_L	0.0074–0.0698
	R2	0.9994
Freundlich	K_F (mg/g)	124.95
	n	4.97
	R2	0.8528
Temkin	K_T (mg/L)	27.90
	b_T (J/mol)	0.0160
	R2	0.9317
Dubinin–Radushkevich	q_max (mg/g)	313.97
	E (kJ/mol)	1346
	R2	0.9643
Harkins–Jura	A	27778
	B	2.306
	R2	0.6313

Figure 12

Isotherm data of Pb2+ adsorption on MC-g-PAA fitted using the Langmuir model.

It is evident from Table 2 that the correlation coefficient value of the Langmuir isotherm model (0.9994) was higher than that of other isotherm models, which clearly indicates that the Langmuir isotherm model better fitted the isotherm data. Therefore, the results show that the adsorption of Pb2+ on MC-g-PAA is monolayer adsorption and the distribution of carboxyl group grafted corncobs via ATRP were homogeneous. The values of were calculated to be between 0.0074 and 0.0698, indicating that the adsorption of Pb2+ from aqueous solutions using MC-g-PAA can be favorable within the concentration range of 50–500 mg/L. In addition, the theoretical maximum amount () of Pb2+ adsorbed on MC-g-PAA has been determined as 342.47 mg/g, which is in good agreement with the experimental value (341.34 mg/g) and 21.11 times greater than the value of pristine corncobs (16.22 mg/g) [18]. The results confirmed that the introduction of brushes with high densities of carboxyl groups onto the corncobs could significantly enhance the adsorption capacity of corncobs for Pb2+.

Table 3 shows that many modified adsorbents have been applied to the adsorption of Pb2+ from aqueous solutions, and some of these adsorbents have been reported to have high adsorption capacity for Pb2+ in recent years. Obviously, the adsorption capacity for Pb2+ of MC-g-PAA was higher than those of other adsorbents and much higher than those of the adsorbents with corncobs as the raw materials. Hence, it can be concluded that the MC-g-PAA synthesized via ATRP herein has strong competitive advantages for the adsorption of Pb2+ from aqueous solutions.

Table 3

Comparison of adsorption capacities for Pb2+ reported in the literature.

Raw Material	Adsorbent	q_max (mg/g)	References
Corncobs	MC-g-PAA	342.47	Present study
	Pristine corncobs	16.22	[18]
	Hydrolyzed corncobs	43.41
	Esterified corncobs	7.89
	Corn cob-kaolinite clay	23.26	[32]
	Acid-modified Activated Carbon (Corncob)	29.47	[33]
Other materials	Discarded mushroom-stick biochar (DMB8)	21.0	[34]
	AMPS-modified hazelnut shell powder	32.74	[35]
	Ternary nanocomposite (TNC)	79.56	[36]
	Phosphate-modified baker’s yeast (PMBY)	92	[37]
	Fe-Mn binary oxides-loaded biochar (BFM)	113.72	[20]
	Chitosan-Modified fast pyrolysis BioChar (CMBC)	134	[38]
	Non-Modified BioChar (NMBC)	48.2
	Biochar(BC) made from dairy manure	175.53	[39]
	Silver wattle tannin resins	189.30	[30]
	Black wattle tannin resins	105.70
	Green wattle tannin resins	98.82
	Vanadium (V)-doped materials	194.15–237.45	[40]

3.7. Adsorption Kinetics

The adsorption rate is one of the most important features of the adsorbent; therefore, the effect of sorption time was studied between 0 and 180 min in this study. The results of Pb2+ adsorption on MC-g-PAA are shown in Figure 13. It can be seen that adsorption is a very fast process. The adsorption capacity of Pb2+ on MC-g-PAA increased rapidly in the first 15 min, contributing to 68.82% at 1 min and 98.49% of the overall adsorption capacity (324.68 mg/g) at 15 min. The continuing increase was slower and approached the adsorption equilibrium after 15 min. The rapid adsorption rate reflects the good accessibility of Pb2+ binding sites on MC-g-PAA, which is beneficial in practical application, since it results in a reduction of reactor volumes and time.

Figure 13

Effect of sorption time on the adsorption of Pb2+ on MC-g-PAA.

In order to evaluate the kinetic mechanism, the experimental kinetic adsorption data were analyzed by using six models: the pseudo-first-order, pseudo-second-order, intra-particle diffusion, Elovich, liquid-film diffusion, and Avrami-fractional kinetic models. The linearized pseudo-first-order kinetic model can be written as [41]: where (min) represents the sorption time; (mg/g) is the amount of Pb2+ adsorbed per unit mass of the adsorbent at min; and (min−1) is the adsorption rate constant of the pseudo-first-order model. The and values were determined from the slope and intercept of the linear plot between and .

The linearized pseudo-second-order kinetic model is given by [2,41]: where (g/mg/min) represents the adsorption rate constant of the pseudo-second-order model. The values of and were evaluated from the slope and intercept of the linear plot between and .

The initial adsorption rate (h) was determined as follows [41]:

The linearized intra-particle diffusion kinetic model is represented by [30,42,43,44]: where (mg/g/min0.5) represents the intra-particle diffusion rate constant and is the intercept related to the thickness of the boundary layer. The values of and were evaluated from the slope and intercept of the linear plot between and .

The linearized Elovich kinetic model is defined by [44,45]: where (min/mg/g) and (g/mg) are constants of the Elovich model. The and values were estimated from the slope and intercept of the linear plot between and .

The linearized Avrami-fractional kinetic model is represented by [43]: where and are constants of the Avrami-fractional model. The and values were estimated from the slope and intercept of the linear plot between and .

Kinetic parameters for the adsorption of Pb2+ on MC-g-PAA and the correlation coefficients (R2) of these kinetic models are given in Table 4.

Table 4

Kinetic parameters for the adsorption of Pb2+ on MC-g-PAA.

Model	Parameter	Value
Experimental data	q_e (mg/g)	323.65
First-order	q_e (mg/g)	320.51
	k_1 (min−1)	0.4808
	R2	0.90174
Second-order	q_e (mg/g)	324.68
	k_2 (g/mg/min)	0.00561
	h (mg/g/min)	591.72
	R2	0.99999
Intra-particle diffusion	k_F (mg/g/min0.5)	5.121
	C	272.7
	R2	0.4577
Elovich	α	3.41 × 107
	β	0.0578
	R2	0.7508
Avrami-fractional	n_AV	0.4713
	K_AV	1.020
	R2	0.9142

Table 4 shows that the correlation coefficient value of the pseudo-second-order kinetic model (0.99999) was higher than that of other kinetic models. The linear plot of the pseudo-second-order kinetic model is shown in Figure 14.

Figure 14

Kinetic data for the adsorption of Pb2+ on MC-g-PAA fitted using the pseudo-second-order kinetic model fitted for the kinetic adsorption data.

Obviously, the pseudo-second-order kinetic model provides a better fit for experimental kinetic adsorption data than that of the other five models, which suggests that the adsorption process is dominated by chemical adsorption involving complexation and electrostatic interactions [4].

The , , and values of the pseudo-second-order model were found to be 0.00561 g/mg/min, 591.72 mg/g/min, and 324.68 mg/g, respectively. The initial adsorption rate () was extremely high, indicating that the adsorption of Pb2+ on MC-g-PAA is a rapid process. The theoretical value was in good agreement with the experimental value (323.66 mg/g).

4. Conclusions

The brushes with dense and active carboxyl groups (–COOH) was successfully introduced onto the corncobs via the ATRP technique, obtaining functionalized corncobs (MC-g-PAA) as novel adsorbents, which were characterized by FTIR and SEM. The solid/liquid ratio and solution pH had strong effects on the adsorption of Pb2+, and their optimum values were determined as 0.20 g/(75 mL) and 5.0, respectively. Thermodynamic studies showed that the adsorption capacity of Pb2+ on MC-g-PAA increased slowly with the increase of sorption temperature. Furthermore, this adsorption process was spontaneous, endothermic, and accompanied by an increase in randomness. The Langmuir model provided a better fit for the isotherm data than the Freundlich model and the maximum amount () of Pb2+ adsorbed on MC-g-PAA was 342.47 mg/g, which was 21.11 times greater than the of the pristine corncobs (16.22 mg/g). Kinetic studies showed that adsorption was a very fast process, which approached an equilibrium after 15 min, and that the experimental data had the best agreement with the pseudo-second-order equation. The monolayer adsorption process of Pb2+ on MC-g-PAA was dominated by chemical adsorption, and may proceed according to complexation and electrostatic interactions between Pb2+ and the carboxylate groups.