Evaluation of the Adsorption Efﬁciency on the Removal of Lead(II) Ions from Aqueous Solutions Using Azadirachta indica Leaves as an Adsorbent

: The efﬁciency of Azadirachta indica (neem leaves) on the removal of Pb(II) ions by adsorption from aqueous solution was investigated in this study. The efﬁciency of these leaves (without chemical or thermal treatment) for the adsorption of Pb(II) ions has not previously been reported. Batch experiments were performed to study the effect of the particle size, pH, adsorbent dose, contact time, initial Pb(II) ion concentration, and temperature. The maximum removal of 93.5% was achieved from an original Pb(II) ion solution concentration of 50 mg/L after 40 min, at pH 7, with 0.60 g of an adsorbent dose. The maximum adsorption capacity recorded was 39.7 mg/g. The adsorption process was also studied by examining Langmuir, Freundlich, Temkin isotherm, and Dubinin–Radushkevich (D-R) isotherm models. The results revealed that the adsorption system follows the pseudo-second-order model and ﬁtted the Freundlich model. Several thermodynamic factors, namely, the standard free energy ( ∆ G ◦ ), enthalpy ( ∆ H ◦ ), and entropy ( ∆ S ◦ ) changes, were also calculated. The results demonstrated that the adsorption is a spontaneous, physical, and exothermic process. The surface area, pore size, and volume of adsorbent particles were measured and presented using a surface area analyzer (BET); the morphology was scanned and presented with the scanning electron microscope technique (SEM); and the functional groups were investigated using µ -FTIR.


Introduction
Industrial activities have significantly contributed to environmental pollution. Toxic metals are one of the major pollutants causing serious damage to the environment, in addition to being a documented source of many diseases [1]. The heavy metal pollutants in wastewater are highly toxic, hazardous to plants and animals, and result in a shortage of clean water [2,3]. Lead is among these toxic elements, and has acute and chronic health effects on humans [4]. Lead pollution affected nearly 18-22 million people in 2010, motivating an investigation of water purification processes [5].
With respect to metal removal, wastewater purification includes various methods, such as biosorption, adsorption, electrochemical treatments, and oxidation [6,7]. Heavy metal biosorption is one of the favorable fields of remedy due to the low cost and easy

Batch Adsorption Experiment
Batch experiments were performed using 250 mL stoppered bottles containing the desired mass at a pH of 5.5 with 50 mL of Pb(II) solution (50 mg/L). The mixture was shaken at 298 K (except when examining the temperature effect) by a temperature-controlled water bath shaker. At the end of the shaking time, the solid adsorbent was isolated from the solution by filtration, and the remaining concentration of Pb(II) ions was then determined using an atomic absorption spectrometer (AAS) (SpectrAA 220, Varian, UK). Parameters influencing the sorption efficiency were investigated by changing one factor and keeping the others constant. The adsorption extent was determined using Equation (1): where V is the volume of the Pb(II) solution in the bottle, q e is the metal uptake capacity (mg/g), M is the mass of AILP (g), C o is the initial Pb(II) concentration, and C e is the Pb(II) concentration at equilibrium. The total removal efficiency (R%) was calculated using Equation (2).
Processes 2021, 9,559 3 of 15 The investigated parameters, including the particle size, shaking time, mass of adsorbent, temperature, and solution concentration, were investigated.

Characterization of AILP
The surface area, pore-volume, and pore size were investigated using a Quanta Chrome NOVA 4200E Surface Area Analyzer. The morphology of the powder was examined using a Jeol 6360 (Japan) scanning electron microscope at an accelerating voltage of 20 kV. The functional groups of the powder before and after adsorption were investigated by µ-FT-IR (Cary 630 FTIR from Agilent, Santa Clara, USA) in the range of 400-4000 cm −1 at a spectral resolution of 8 cm −1 .

Reusability of AILP
AILP was reactivated by vigorous shaking in an excess quantity of de-ionized water for 12 hrs. AILP was separated by filtration and then dried by heating it overnight at 105 • C. The optimal conditions were maintained throughout all reusability experiments.

Surface Area of AILP
The AILP sample exhibited a high surface area of 183 m 2 /g, enhancing its adsorption capabilities. The results revealed that the average pore diameter is 10.3 nm and the total pore volume is 0.355 cm 3 /g. Comparative data are given in Table 1. These data demonstrate that the AILP surface area is larger than that of the reported sorbents, indicting a high adsorption capacity.

IR Spectrum
The µ-FT-IR spectrum is used to estimate the contribution of functional groups on the adsorbent surface in the adsorption process. The FT-IR analysis was performed before and after the adsorption process ( Figure 1). The results revealed distinguished bands of Pb-O stretching vibrations that appeared at 462 cm −1 and OH stretching of the hydroxide groups. These bands may confirm the adsorption of Pb(II) ions on the adsorbent surface. Other bands appeared at 1298, 1350, and 1723 cm −1 , and these bands are probably related to the stretching of -C-N-, -C=N-, and -C=C-, respectively, in polyheterocycles. However, the FT-IR spectra of the adsorbent before and after adsorption were very similar due to the physisorption process.

Scanning Electron Microscope (SEM)
The SEM images of AILP before and after adsorption are presented in Figure 2. The SEM images illustrate differences in the surface morphologies of the AILP surfaces before and after adsorption. The surface of the AILP before adsorption showed micro flakes with an approximate size of 0.5 μm (Figure 2a). Additionally, the analysis of the AILP surface after adsorption revealed differences in the surface structure and the adsorption process led to the formation of many floccules and spots due to the adsorption of Pb(II) ions on the AILP surface, leading to a rough appearance.

Effect of the Adsorbent Particle Size
The removal efficiency of Pb(II) ions from aqueous solutions by the AILP increased from 82.9% to 99.1% as the AILP size decreased from 800 to 100 μm, at 298 K, for a 50 mg/L initial Pb(II) ions concentration (Figure 3). With a decrease in AILP particle sizes, the surface area of the AILP increased, so the number of active sites accessible on the AILP surface had a better exposure to the adsorbate. Similar findings have also been reported by other researchers [12].

Scanning Electron Microscope (SEM)
The SEM images of AILP before and after adsorption are presented in Figure 2. The SEM images illustrate differences in the surface morphologies of the AILP surfaces before and after adsorption. The surface of the AILP before adsorption showed micro flakes with an approximate size of 0.5 µm (Figure 2a). Additionally, the analysis of the AILP surface after adsorption revealed differences in the surface structure and the adsorption process led to the formation of many floccules and spots due to the adsorption of Pb(II) ions on the AILP surface, leading to a rough appearance.

Scanning Electron Microscope (SEM)
The SEM images of AILP before and after adsorption are presented in Figure 2. The SEM images illustrate differences in the surface morphologies of the AILP surfaces before and after adsorption. The surface of the AILP before adsorption showed micro flakes with an approximate size of 0.5 μm (Figure 2a). Additionally, the analysis of the AILP surface after adsorption revealed differences in the surface structure and the adsorption process led to the formation of many floccules and spots due to the adsorption of Pb(II) ions on the AILP surface, leading to a rough appearance.

Effect of the Adsorbent Particle Size
The removal efficiency of Pb(II) ions from aqueous solutions by the AILP increased from 82.9% to 99.1% as the AILP size decreased from 800 to 100 μm, at 298 K, for a 50 mg/L initial Pb(II) ions concentration (Figure 3). With a decrease in AILP particle sizes, the surface area of the AILP increased, so the number of active sites accessible on the AILP surface had a better exposure to the adsorbate. Similar findings have also been reported by other researchers [12].

Effect of the Adsorbent Particle Size
The removal efficiency of Pb(II) ions from aqueous solutions by the AILP increased from 82.9% to 99.1% as the AILP size decreased from 800 to 100 µm, at 298 K, for a 50 mg/L initial Pb(II) ions concentration (Figure 3). With a decrease in AILP particle sizes, the surface area of the AILP increased, so the number of active sites accessible on the AILP surface had a better exposure to the adsorbate. Similar findings have also been reported by other researchers [12].

Effect of the pH
The maximum adsorption was achieved at pH 5.0 ( Figure 4). It is presidentially noted that with a pH higher than 5.0, the adsorption activity decreased sharply. However, at pH values lower than 5.0, the adsorption process could be hindered by the existence of a high concentration of positive hydrogen ions, and the adsorption sites became positively charged, exerting a repelling effect on the Pb(II) cations. With an increase in the pH, the negative charge density on AILP increased as a result of deprotonation of the metal-binding sites, hence increasing the metal uptake; such findings are in agreement with previous studies. It is well-known that lead ions start to precipitate above pH 5.0-6.0 in the form of Pb(OH)2, suppressing the adsorption of lead ions [1].

Effect of the pH
The maximum adsorption was achieved at pH 5.0 ( Figure 4). It is presidentially noted that with a pH higher than 5.0, the adsorption activity decreased sharply. However, at pH values lower than 5.0, the adsorption process could be hindered by the existence of a high concentration of positive hydrogen ions, and the adsorption sites became positively charged, exerting a repelling effect on the Pb(II) cations. With an increase in the pH, the negative charge density on AILP increased as a result of deprotonation of the metal-binding sites, hence increasing the metal uptake; such findings are in agreement with previous studies. It is well-known that lead ions start to precipitate above pH 5.0-6.0 in the form of Pb(OH) 2 , suppressing the adsorption of lead ions [1].

Effect of the pH
The maximum adsorption was achieved at pH 5.0 ( Figure 4). It is presidentially noted that with a pH higher than 5.0, the adsorption activity decreased sharply. However, at pH values lower than 5.0, the adsorption process could be hindered by the existence of a high concentration of positive hydrogen ions, and the adsorption sites became positively charged, exerting a repelling effect on the Pb(II) cations. With an increase in the pH, the negative charge density on AILP increased as a result of deprotonation of the metal-binding sites, hence increasing the metal uptake; such findings are in agreement with previous studies. It is well-known that lead ions start to precipitate above pH 5.0-6.0 in the form of Pb(OH)2, suppressing the adsorption of lead ions [1].

Effect of the Adsorbent Dosage
To investigate the effect of the sorbent mass on the efficiency of the adsorption process, a series of batch experiments were conducted with various sorbent masses of 0.05, 0.10, 0.20, 0.30, 0.40, 0.60, 0.80, and 1.0 g per 50 mL of aqueous solution of Pb(II) ions. The effect is presented in Figure 5. As the mass of the sorbent increased, the adsorption efficiency also increased. This can be attributed to an increase in the AILP surface area with its mass. The maximum adsorption efficiency for Pb(II) ions was achieved at 0.60 g/50 mL. From the results, it is clear that an increase in the adsorbent mass above 0.6 g had no effect on the adsorption efficiency of Pb(II) ions from the aqueous solution. 0.10, 0.20, 0.30, 0.40, 0.60, 0.80, and 1.0 g per 50 mL of aqueous solution of Pb(II) ions. The effect is presented in Figure 5. As the mass of the sorbent increased, the adsorption efficiency also increased. This can be attributed to an increase in the AILP surface area with its mass. The maximum adsorption efficiency for Pb(II) ions was achieved at 0.60 g/50 mL. From the results, it is clear that an increase in the adsorbent mass above 0.6 g had no effect on the adsorption efficiency of Pb(II) ions from the aqueous solution.

Effect of the Agitation Time
The effect of the agitation time on the adsorption of Pb(II) ions using the AILP is presented in Figure 6. The results showed that the time of 40 min was sufficient for achieving the optimum adsorption, without any influence from increasing the contact time. As demonstrated in Figure 6, the adsorption process could be divided into three phases. The first phase was significantly fast, representing about 88% removal within 30 min. The second phase showed slower adsorption. The first stage was caused by the large surface area of the AILP. With the progressive occupation of these sites, the process became slower in the second stage due to less adsorption sites being available for Pb(II) ions. The third phase was the desorption of Pb(II) ions from the AILP surface. Some of the adsorbed Pb(II) ions might have leached from the AILP into the solution and this is probably a result of the long agitation time.

Effect of the Agitation Time
The effect of the agitation time on the adsorption of Pb(II) ions using the AILP is presented in Figure 6. The results showed that the time of 40 min was sufficient for achieving the optimum adsorption, without any influence from increasing the contact time. As demonstrated in Figure 6, the adsorption process could be divided into three phases. The first phase was significantly fast, representing about 88% removal within 30 min. The second phase showed slower adsorption. The first stage was caused by the large surface area of the AILP. With the progressive occupation of these sites, the process became slower in the second stage due to less adsorption sites being available for Pb(II) ions. The third phase was the desorption of Pb(II) ions from the AILP surface. Some of the adsorbed Pb(II) ions might have leached from the AILP into the solution and this is probably a result of the long agitation time.

Adsorption Kinetics
The aim of investigating the adsorption kinetics is to explore the mechanism of adsorption and evaluate the efficiency of the adsorbent. The pseudo-first-order, pseudo-second-order, and intra-particle diffusion kinetic models were used to investigate the obtained data on the adsorption of Pb(II) ions on the AILP.

Pseudo-First-Order Kinetic Model
The equation of this model is given by Equation (3): where qe is the amount of solute (mg/g) removed at equilibrium, qt is the quantity of solute adsorbed at any time (t), and k is the rate constant. It was found that the data do not fit this model (R 2 = 0.0006).

Adsorption Kinetics
The aim of investigating the adsorption kinetics is to explore the mechanism of adsorption and evaluate the efficiency of the adsorbent. The pseudo-first-order, pseudosecond-order, and intra-particle diffusion kinetic models were used to investigate the obtained data on the adsorption of Pb(II) ions on the AILP. The equation of this model is given by Equation (3): where q e is the amount of solute (mg/g) removed at equilibrium, q t is the quantity of solute adsorbed at any time (t), and k is the rate constant. It was found that the data do not fit this model (R 2 = 0.0006).

Pseudo-Second-Order Kinetic Model
The equation of this model is A typical plot of the pseudo-second-order equation is shown in Figure 7. The straight line in the plot proves that the experimental data appropriately obey the pseudo-secondorder model. Values of q e and k 2 were determined from the intercept and slope of Figure 8. These parameters and the correlation coefficient are presented in Table 2. This agrees with previous results and explanations [1,25]. It can be concluded from previous studies that the adsorption kinetics model was governed by the adsorbent nature.

Intra-Particle Diffusion Kinetic Model
This model is shown by Equation (5): where kid is the intra-particle diffusion rate constant, mg/g/min 1/2 . The value of (kid) was calculated from Equation (5) and is presented in Table 2. The relationship between qt and t 1/2 was not linear over the entire time range. The first curved part of the plot can be attributed to the boundary layer diffusion effects and it represents intra-particle diffusion controlled by the rate constant kid (Figure 8).

Intra-Particle Diffusion Kinetic Model
This model is shown by Equation (5): where k id is the intra-particle diffusion rate constant, mg/g/min 1/2 . The value of (k id ) was calculated from Equation (5) and is presented in Table 2. The relationship between qt and t 1/2 was not linear over the entire time range. The first curved part of the plot can be attributed to the boundary layer diffusion effects and it represents intra-particle diffusion controlled by the rate constant k id (Figure 8).

Effect of the Initial Pb(II) Concentration
The effect of the initial concentration of Pb(II) ions on the adsorption efficiency is presented in Figure 9, where it is evident that the adsorption efficiency of Pb(II) ions decreased as the initial Pb(II) ion concentration increased. The decrease in adsorption efficiency can be attributed to the deficiency of sufficient adsorption sites for accumulating the large increase of metal ions available in the solution [21].

Adsorption Isotherm
The adsorption isotherm models were investigated to explore the interaction mechanism of Pb(II) ions on the adsorbent sites [1,21]. The adsorption isotherm models were analyzed by specific parameters, whose values express the surface characteristics and af-

Kinetic Model Parameters
Pseudo-second-order model q e (mg/g) 3.00 k 2 (g/mg min (

Effect of the Initial Pb(II) Concentration
The effect of the initial concentration of Pb(II) ions on the adsorption efficiency is presented in Figure 9, where it is evident that the adsorption efficiency of Pb(II) ions decreased as the initial Pb(II) ion concentration increased. The decrease in adsorption efficiency can be attributed to the deficiency of sufficient adsorption sites for accumulating the large increase of metal ions available in the solution [21].

Effect of the Initial Pb(II) Concentration
The effect of the initial concentration of Pb(II) ions on the adsorption efficiency is presented in Figure 9, where it is evident that the adsorption efficiency of Pb(II) ions decreased as the initial Pb(II) ion concentration increased. The decrease in adsorption efficiency can be attributed to the deficiency of sufficient adsorption sites for accumulating the large increase of metal ions available in the solution [21].

Adsorption Isotherm
The adsorption isotherm models were investigated to explore the interaction mechanism of Pb(II) ions on the adsorbent sites [1,21]. The adsorption isotherm models were analyzed by specific parameters, whose values express the surface characteristics and af-

Adsorption Isotherm
The adsorption isotherm models were investigated to explore the interaction mechanism of Pb(II) ions on the adsorbent sites [1,21]. The adsorption isotherm models were Processes 2021, 9, 559 9 of 15 analyzed by specific parameters, whose values express the surface characteristics and affinity of the adsorbent towards heavy metal ion adsorption [21]. Out of numerous isotherm models, four were examined for this study, namely, Freundlich, Langmuir, Temkin, and Dubinin-Radushkevich (D-R) models.

Langmuir Isotherm
Equation (6) presents the Langmuir linear equation: The results obtained in this study were fitted to the Langmuir isotherm model to determine the maximum adsorption capacity (q max ) of AILP on Pb(II) ions. The linear plot of C e /q e vs. C e (Figure 10a) obtained indicates the applicability of the Langmuir model. Values of b and q m were calculated graphically from the intercept and slope, respectively, and are presented in Table 3. From the Langmuir isotherm, the adsorption process can be classified as follows: when R L = 0, a favorable process occurs when 0 < R L < 1, linear process occurs when R L = 1, and unfavorable process occurs when R L > 1. The R L values for the initial AILP concentrations were between 0.13 and 0.49, which indicates that the adsorption of Pb(II) ions on AILP is a favorable process.

Freundlich Isotherm
This is an experimental expression used for adsorption on heterogeneous surfaces with the interaction between adsorbed molecules. This model suggests an exponential drop in adsorption energy upon completion of the adsorption centers of the adsorbent.

The linear equation of the Freundlich model is shown by Equation (7) [21]:
ln q e = ln K f + 1 n ln C e , where K f is the relative adsorption capacity of the adsorbent that is related to the bonding energy and n is the heterogeneity element stating the deviancy from the linearity of adsorption. A plot of ln q e versus ln C e was used to confirm the Freundlich adsorption isotherm. Values of K f and n were calculated from the intercept and slope (Figure 10b) and are tabulated in Table 3. An explanation of n, which controls the relationship between the solution concentration and adsorption, is as follows: If n < 1, adsorption is a physical process; if n = 1, adsorption is linear; and if n > 1, adsorption is a chemical process. The obtained n value was found to be 0.60, indicating physical processes.

Temkin Isotherm
In this model, the heat of adsorption AILP molecules in the layer is supposed to decrease linearly with the coverage of the adsorbent surface because of a reduction in the adsorbate-adsorbent interactions. The model is defined by Equation (8): where B = (RT)/b t , R is the universal gas constant, and T is the temperature in Kelvin. The constant b t is associated with the heat of adsorption (J/mol). A is the equilibrium binding constant corresponding to the maximum binding energy.
Values of A and B were determined from the slope and intercept of Equation (6) and Figure 10c and are shown in Table 3. The b t value was 318 J/mol, indicating physical adsorption processes [21].

Dubinin-Radushkevich (D-R) Isotherm
The D-R Isotherm model is commonly used to conclude the mean free energy of the adsorption process [1]. The formula of this model is described by Equation (9): ln q e = ln q max − βε 2 , where ε is defined as T denotes the temperature (K), R is the universal gas constant, and q max and β are D-R isotherm constants. β and q max were obtained from the slope and intercept of Equation (9) and Figure 10d and the values are presented in Table 3.
The mean free energy of adsorption process, E f , is defined as the free energy change when one mole of ions is moved to the solid surface from infinity in solution and was determined from Equation (11). where ɛ is defined as T denotes the temperature (K), R is the universal gas constant, and qmax and β are D-R isotherm constants. β and qmax were obtained from the slope and intercept of Equation (9) and Figure 10d and the values are presented in Table 3.
The mean free energy of adsorption process, Ef, is defined as the free energy change when one mole of ions is moved to the solid surface from infinity in solution and was determined from Equation (11). It is well-established that the Ef value is crucial for predicting the adsorption type. For 8 < Ef < 16 kJ/mol, adsorption is considered a chemisorption process, and, when Ef < 8 kJ/mol, adsorption is classified as a physical process. In this study, the lower value of Ef (2.2 KJ/mol) indicates that the adsorption process was of a physical type. Table 3. Adsorption isotherm constants obtained from the four adsorption isotherm models.

Adsorption Model Isotherm Constants Value
Langmuir qmax (mg/g) 39.7 KL (L/g) 0.021 R 2 0.9756 It is well-established that the E f value is crucial for predicting the adsorption type. For 8 < E f < 16 kJ/mol, adsorption is considered a chemisorption process, and, when E f < 8 kJ/mol, adsorption is classified as a physical process. In this study, the lower value of E f (2.2 KJ/mol) indicates that the adsorption process was of a physical type.

Effect of the Temperature
The temperature effect on the adsorption of Pb(II) ions on AILP was examined at a range from 298 to 318 K and is presented in Figure 11. The results revealed that the adsorption efficiency decreased slightly from 95.9% to 93.4% as the temperature increased from 298 to 318 K. This can be attributed to the possible damage of adsorption sites at elevated temperatures.

Thermodynamic Parameters
Enthalpy ∆H • , free energy ∆G • , and entropy ∆S • changes were determined using Equations (12)- (14): where K D is the distribution coefficient and equivalent to the preliminary Pb(II) concentration (C o ) divided by the final Pb(II) concentration (C e ). Figure 12 shows a linear plot of ln K D versus 1/T. The thermodynamic parameters were determined and are presented in Table 4. The negative value of ∆H • indicates the exothermic nature of the adsorption process. The positive value of entropy (∆S • ) proposes an increased randomness at the solid-solution interface. Negative values of Gibbs free energy (∆G • ) prove that the adsorption process is spontaneous, which becomes more positive with an increase in temperature. Therefore, this indicates that less adsorption occurs at elevated temperatures. This is in good agreement with the results obtained from Figure 10c. were determined and are presented in Table 4. The negative value of ΔH° indicates the exothermic nature of the adsorption process. The positive value of entropy (ΔS°) proposes an increased randomness at the solid-solution interface. Negative values of Gibbs free energy (ΔG°) prove that the adsorption process is spontaneous, which becomes more positive with an increase in temperature. Therefore, this indicates that less adsorption occurs at elevated temperatures. This is in good agreement with the results obtained from Figure  10c.

Reusability of AILP
The results of reusing the AILP are presented in Figure 13. It appeared that the adsorption effectiveness of the AILP decreased gradually with the reusability. The results confirm that the AILP can be efficiently recycled 2-3 times when removing Pb(II) ions from their aqueous solutions. The adsorption efficiency of the AILP decreased to 68.5% when it was reused for a fifth time.

Reusability of AILP
The results of reusing the AILP are presented in Figure 13. It appeared that the adsorption effectiveness of the AILP decreased gradually with the reusability. The results confirm that the AILP can be efficiently recycled 2-3 times when removing Pb(II) ions from their aqueous solutions. The adsorption efficiency of the AILP decreased to 68.5% when it was reused for a fifth time.

Reusability of AILP
The results of reusing the AILP are presented in Figure 13. It appeared that the adsorption effectiveness of the AILP decreased gradually with the reusability. The results confirm that the AILP can be efficiently recycled 2-3 times when removing Pb(II) ions from their aqueous solutions. The adsorption efficiency of the AILP decreased to 68.5% when it was reused for a fifth time.

Possible Adsorption Mechanism
The adsorption of Pb(II) ions on the AILP surface possibly jointly occurs by means of chemical interactions and physisorption. The ATR-FT-IR analysis proves that a Pb-O bond is formed after the adsorption process; on the other hand, values of ∆G • and b t suggest a physisorption process.

Comparison of AILP with Other Sorbents
An evaluation of q max of the AILP according to the reported q max values for other biosorbents is shown in Table 5. Variances in q max can be attributed to the specific nature and properties of each adsorbent, surface area, and construction of the adsorbent. Making this comparison with other adsorbents confirms that AILP is a good and promising adsorbent.

Conclusions
In this study, Azadirachta indica leaves' powder (AILP), which is a natural adsorbent material, eco-friendly, and inexpensive, was investigated. AILP was used for the removal of Pb(II) ions from aqueous solution. The removal efficiency reached above 95%. The powder of the leaves spontaneously retained considerable amounts of Pb(II) ions. The maximum adsorption capacity for neem leaves was determined as being 39.7 mg/g. Experimental investigations defined the optimum conditions for the competent removal of 50 mg/L of Pb(II) ion to be 0.60 g, 40 min of contact time, and a pH of 7. These are significant characteristics for this tested adsorbent, making it an excellent choice for cleaning polluted water due to it (1) being a natural material and (2) cost-effective, as it requires no chemical treatment; (3) its availability, with this material being abundantly available in the region; and (4) its effectiveness, with it being capable of removing Pb(II) ions with a high efficiency. These positive characteristics would make this adsorbent a suitable candidate for removing other poisonous metal ions.

Conflicts of Interest:
The authors declare no conflict of interest.