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Article

Biosorption of Pb(II) Using Natural and Treated Ardisia compressa K. Leaves: Simulation Framework Extended through the Application of Artificial Neural Network and Genetic Algorithm

by
Alma Y. Vázquez-Sánchez
1,
Eder C. Lima
2,
Mohamed Abatal
3,*,
Rasikh Tariq
4,
Arlette A. Santiago
5,
Ismeli Alfonso
6,
Claudia Aguilar
7 and
América R. Vazquez-Olmos
8
1
Área Agroindustrial Alimentaria, Universidad Tecnológica de Xicotepec de Juárez, Av. Universidad Tecnológica No. 1000. Col. Tierra Negra Xicotepec de Juárez, Puebla 73080, Mexico
2
Institute of Chemistry, Federal University of Rio Grande do Sul (UFRGS), Av. Bento Goncalves 9500, P.O. Box 15003, Porto Alegre 91501-970, RS, Brazil
3
Facultad de Ingeniería, Universidad Autónoma del Carmen, Campeche 24115, Mexico
4
Institute for the Future of Education, Tecnologico de Monterrey, Monterrey 64849, Mexico
5
Escuela Nacional de Estudios Superiores, Unidad Morelia, Universidad Nacional Autónoma de México, Antigua Carretera a Pátzcuaro No. 8701, Col. Ex. Hacienda de San José de la Huerta, Morelia 58190, Mexico
6
Instituto de Investigaciones en Materiales, Unidad Morelia, Universidad Nacional Autónoma de México, Antigua Carretera a Pátzcuaro No. 8701, Col. Ex. Hacienda de San José de la Huerta, Morelia 58190, Mexico
7
Facultad de Química, Universidad Autónoma del Carmen, Calle 56 No. 4 Av. Concordia, Ciudad del Carmen, Campeche 24180, Mexico
8
Instituto de Ciencias aplicadas y Tecnología, UNAM, Circuito Exterior, S/N, Ciudad Universitaria, A.P. 70-186, Delegación Coyoacán, Ciudad de México 04510, Mexico
*
Author to whom correspondence should be addressed.
Molecules 2023, 28(17), 6387; https://doi.org/10.3390/molecules28176387
Submission received: 12 July 2023 / Revised: 15 August 2023 / Accepted: 23 August 2023 / Published: 31 August 2023

Abstract

:
This study explored the effects of solution pH, biosorbent dose, contact time, and temperature on the Pb(II) biosorption process of natural and chemically treated leaves of A. compressa K. (Raw-AC and AC-OH, respectively). The results show that the surface characteristics of Raw-AC changed following alkali treatment. FT-IR analysis showed the presence of various functional groups on the surface of the biosorbent, which were binding sites for the Pb(II) biosorption. The nonlinear pseudo-second-order kinetic model was found to be the best fitted to the experimental kinetic data. Adsorption equilibrium data at pH = 2–6, biosorbents dose from 5 to 20 mg/L, and temperature from 300.15 to 333.15 K were adjusted to the Langmuir, Freundlich, and Dubinin–Radushkevich (D-R) isotherm models. The results show that the adsorption capacity was enhanced with the increase in the solution pH and diminished with the increase in the temperature and biosorbent dose. It was also found that AC-OH is more effective than Raw-AC in removing Pb(II) from aqueous solutions. This was also confirmed using artificial neural networks and genetic algorithms, where it was demonstrated that the improvement was around 57.7%. The nonlinear Langmuir isotherm model was the best fitted, and the maximum adsorption capacities of Raw-AC and AC-OH were 96 mg/g and 170 mg/g, respectively. The removal efficiency of Pb(II) was maintained approximately after three adsorption and desorption cycles using 0.5 M HCl as an eluent. This research delved into the impact of solution pH, biosorbent characteristics, and operational parameters on Pb(II) biosorption, offering valuable insights for engineering education by illustrating the practical application of fundamental chemical and kinetic principles to enhance the design and optimization of sustainable water treatment systems.

1. Introduction

Over recent decades, heavy metals have been monitored in sediments, soils, and water systems in different regions of the world in order to study their risks to wildlife and human health [1,2,3]. In these studies, the reported concentrations of various toxic metals, such as chromium (Cr), mercury (Hg), lead (Pb), nickel (Ni), and cadmium (Cd), exceed the permissible limits according to the United States Environmental Protection Agency (US-EPA) and World Health Organization (WHO) [1]. In the previous investigations, urban sewage and effluents discharged from different manufacturers like pigment, battery, and pesticides or mining activities are considered the principal sources of these hazardous metals in the monitored sites [1]. The presence of toxic metals, even at low concentrations in soils and water, can cause severe animal and human health risks, even cancer and other diseases, such as respiratory irritation, bronchial spasms, and coughing [4,5,6]. Therefore, intense investigations have developed various industrial and urban wastewater treatment techniques, including coagulation, chemical precipitation, reverse osmosis, ion exchange, flocculation, and membrane filtration, that are used before the waste products are discharged into the aquatic system [7]. Among these methods, adsorption has become the most used technique for removing organic or inorganic pollutants due to its simplicity, high efficiency, and low cost [8]. Numerous adsorbents have been developed for Pb(II) ion removal, such as zeolites [9], kaolinite clay [10], carbon-based materials [11], agricultural waste [12], and polymeric materials [13]. The cost and availability of the adsorbent materials are crucial to the efficiency of the adsorption technique. In this regard, many agriculture and industrial waste materials have been widely used to remove heavy metals from wastewater due to their low cost, availability, and the possibility for generation over various adsorption/desorption cycles [14,15,16,17]. A number of agro-wastes were studied for the adsorption of Pb (II) from aqueous solution, such as Azadirachta indica leaves [18], Tamarindus indica seeds [19], and rape straw [20], as a result of their chemical components namely, steroids, saponins, flavonoids, alkaloids, tannins, and amino acid [21]. Recent investigations reported that chemical modification increased the number of binding ligand groups on the biosorbent’s surface. Therefore, the adsorption capacity of biosorbents is expected to be enhanced because the heavy metal ion uptake is favored by increasing active sites on the biosorbent’s surface [22].
A. compressa K. belongs to the Myrsinaceae family, which is found in tropical and subtropical regions and has been used as food and folk medicine in different parts of the world [23]. In Mexico, A. compressa K. is found in different states, such as Aguascalientes, Chiapas, Chihuahua, Guerrero, Hidalgo, Jalisco, Michoacán, Nayarit, Oaxaca, Puebla, Tlaxcala, San Luis Potosí, Sinaloa, Tamaulipas, and Veracruz [24]. Notably, in the North of Puebla, it is known as Acachul, and recent investigations reported by Vázquez-Sánchez A.Y. et al. [24] and by Joaquín-Cruz, Elvia et al. [23] showed that A. compressa K. fruits contain various phytochemicals like anthocyanins, polyphenols, flavonoids, diterpenes, gallotannins, and chlorogenic acids. In contrast, Chandra and Mejia [25] identified the presence of phenolic constituents, such as catechin, epicatechin gallate, gallic acid, kaempferol, and ardisin, in the aqueous extracts of the leaves of A. compressa K. Therefore, A. compressa K. biomass can be considered as an alternative potential biosorbent for heavy metal removal from water due to its interesting properties and its availability.
Another novel aspect of this research is to resolve such a multivariate problem to find the optimal combination of all the tuning variables for the maximization of the removal fraction. This is attained through the application of artificial neural networks for the regression model and the genetic algorithm for optimization purposes.
To the best of our knowledge, A. compressa K. biomass has not been used as a biosorbent. Thus, this work contributes to studying the biosorption capacity of natural and treated-with-NaOH A. compressa K. leaves regarding removing Pb(II) from aqueous solutions varying solution pH, contact time, adsorbent dose, and temperature. In addition, the adsorption–desorption cycle experiments studied the reuse of raw and treated biosorbents.

2. Results and Discussion

2.1. Physicochemical Characterization

Table 1 presents the physicochemical parameters of A. compressa K. leaves in a sense to determine their nutritional composition. The results are in agreement with various reports of the proximate chemical composition of the other biosorbents, such as Leucaena leucocephala leaves [26,27] and Nostoc commune [28]. For example, if we compare our results with those reported for Leucaena leucocephala leaves, the ash content was higher than the 5.35% reported by Thamaga et al. (2021) [26] but lower than the 6.62% reported by G.W. Garcia et al. (2013) [27]; likewise, the protein contents were lower than 19.53% and 22.03% [26,27]. These variations could be attributed to differences in the ages of trees, agro-climatic conditions, and maturity stages [29]. Also, based on the results and in comparison, N. commune samples had a high moisture content (96.52 ± 0.11%) and high amounts of non-nitrogen-containing components (69.56 ± 0.09%) compared with A. compressa K. leaves. Furthermore, the values of the crude fat (0.24 ± 0.02%), crude fiber (3.42 ± 0.06%), and ash (5.25 ± 0.08%) were lower than A. compressa K. leaves [30].

2.2. Characterization

2.2.1. Zero-Point Charge

Figure 1 shows the initial pH (pHinitial) variation vs. the final pH (pHfinal) of Raw-AC and AC-OH biosorbents. As can be observed from Figure 1, the intersection of the diagonal line and the pHinitial vs. pHfinal curves indicates that the pHPZC values of Raw-AC and AC-OH were 4.8 and 6.4, respectively. The increase in the pHPZC after the alkali treatment of Raw-AC confirmed the modification in its surface charge, which might improve the biosorption of metal ions since when pH > pHPZC, the surface becomes negative, whereas it is positive when pH < pHPZC. Similar results were obtained and are presented in Table 2, where the pHPZC values of some raw biosorbents increased with alkaline treatment.

2.2.2. Scanning Electron Microscopy

The chemical composition before and after contact with the Pb(II) solution of the RAW-AC and AC-OH samples was estimated using energy-dispersive X-ray (EDX) spectroscopy. Both samples show mainly the presence of carbon (C), oxygen (O), calcium (Ca), and aluminum (Al). The EDX analysis results show that the amount of Pb was 4.4 Wt% for the RAW-AC sample, whereas for the AC-OH sample, the Pb adsorbed was 7.5% Wt%. These results and their corresponding SEM images of RAW-AC and AC-OH before and after contact with Pb (II) are presented in Figure 2 and Figure 3, respectively. For both samples, the presence of Pb (II) is clear in the zoomed-in image, as represented by red dots.

2.2.3. FTIR Analysis

Fourier transform infrared (FTIR) analysis of the biosorbent samples was performed to confirm the presence of functional groups. Figure 4 shows the bands corresponding to the identified functional groups in the biosorbents. The broad band, observed from 3310 to 3280 cm−1 for both the before-biosorption and after-biosorption samples, indicates the presence of -OH and -N-H groups [35]. The bands at 2920, 2900, and 2850 cm−1 represent the existence of methyl and methylene groups. The bands at 1730 and 1610 cm−1 represent the characteristics of the carbonyl group (C=O) stretching from aldehydes and ketones, which could be conjugated or non-conjugated to aromatic rings [36]. The bands at 1450 cm−1 show CH2 and CH3 groups, while the 1160 and 1220 cm−1 bands illustrate C-N [37]. The band at 1610 cm−1 was shifted to 1590 cm−1 after the Pb(II) uptake, suggesting the interaction of the carbonyl group with Pb(II) during the biosorption process. The A. compressa K. has a band at 1030 cm−1 and was assigned to the stretch of the C-O group of ether or ester. After the Pb(II) uptake, this band was shifted to 1020 cm−1, indicating the interaction of biomass with Pb(II) [38]. As expected, the surface of the biosorbents contains different functional groups, such as carboxyl, hydroxyl, and amino groups, which could be a potential adsorption site for biosorption.

2.3. Biosorption Results

2.3.1. Effect of Solution pH

The effect of the solution pH on the Pb(II) sorption capacity of Raw-AC and AC-OH was studied using the isotherm experiments. Figure 5 shows the isotherm adsorption of Pb(II) for solution pHs at 2, 4, and 6. As observed, the Pb(II) sorption capacity of Raw-AC and AC-OH increased with the increase in adsorbate solution pH. This dependence can be associated with the metal species present at different pH solutions and the biosorbent’s surface charge [39].
The lower removal of Pb(II) at acidic pH (pH = 2 and 4) can be attributed to two reasons: (a) the competition between H+ present in the solution and Pb2+ ions that are the predominant species in this pH region, and (b) the electrostatic repulsion between the Pb2+ and the positively charged surface of Raw-AC and AC-OH biosorbents because the solution pH was lower than pHPZC(Raw-AC) = 4.8 and pHPZC(AC-OH) = 6.4. At pH = 6, the capacity of adsorption of biosorbents was superior when compared with pH = 2 and 4; this can be explained by the decrease in competition between protons and cations of Pb on the surface of the biosorbent due to the lower number of protons in the solutions. Furthermore, at pH = 6, the surfaces of biosorbents became negative, and the biosorption of Pb ions was favored over the ionic states of the carboxyl, hydroxyl, and amino groups [40].
Table 3 gives the parameter values of the Langmuir, Freundlich, and Dubinin–Radushkevich isotherm models using their non-linear forms (Equations (4), (5), and (6), respectively). Comparing the correlation coefficients (R2) obtained from the nonlinearized Langmuir, Freundlich, and Dubinin–Radushkevich isotherm models, the Langmuir model was the best fitted to the experimental equilibrium data.
For Raw-AC, at pH = 2, R2(Langmuir) = 0.981 > R2(Freundlich) = 0.960 > R2(Dubinin–Radushkevich) = 0.897; at pH = 4, R2(Langmuir) = 0.992 > R2(Freundlich) = 0.970 > R2(Dubinin–Radushkevich) = 0.932; and at pH = 6, R2(Langmuir) = 0.997 > R2(Freundlich) = 0.972 > R2(Dubinin–Radushkevich) = 0.910.
For AC-OH, at pH = 2, R2(Langmuir) = 0.971 > R2(Freundlich) = 0.924 > R2(Dubinin–Radushkevich) = 0.917; at pH = 4, R2(Langmuir) = 0.984 > R2(Freundlich) = 0.913 > R2(Dubinin–Radushkevich) = 0.867; and at pH = 6, R2(Langmuir) = 0.990 > R2(Freundlich) = 0.976, > R2(Dubinin–Radushkevich) = 0.913.
At pH = 2, 4, and 6, the maximum sorption capacities of Raw-AC determined from the Langmuir model (Qm) were 26.4, 48.1, and 96.4 mg/g, whereas, for AC-OH, the Qm values were 43.7, 49.6, and 170.9 mg/g, respectively. As shown in Table 3, the values of KL for both biosorbents decreased with the increase in solution pH (from 2.001.10−2 to 0.781.10−2 L/mg for Raw-AC and from 59.431.10–2 to 9.076 10−2 L/mg for AC-OH), indicating that the adsorption of Pb(II) was not favored in an acidic solution. Similar results were reported using other biosorbents [39,40].
The values of the average relative error (ARE), the sum of square error (SSE), normalized standard deviation Δq (%), chi-squared test (χ2), the sum of absolute error (EABS), and the root mean square error (RMSE) are presented in Table 4.
Comparing the values calculated for both isotherm models, it can be observed that the lower values of all error functions were obtained for the nonlinearized Langmuir model, confirming the same result predicted using correlation coefficient nonlinear analysis.

2.3.2. Adsorbent Mass Effect

The effect of biosorbent mass on the adsorption of Pb(II) was explored using isotherm experiments. Figure 6 shows that the Pb(II) adsorption isotherms for doses of Raw-AC and AC-OH that varied from 5 to 20 g/L. The experimental data graphs were plotted alongside nonlinear Langmuir and Freundlich isotherm models.
The removal percentage of Pb(II) was found to increase by increasing the biosorbent dose and decrease with increasing of initial concentration of Pb(II). For example, at Ci Pb(II) = 500 mg/L, the removal percentages of Pb(II) by Raw-AC and AC-OH were found to be 52.59–89.47%, 76.04–99.83%, and 86.07–99.76% at a doses of 5, 15, and 20 g/L, respectively. This result can be explained by the increase in the number of adsorption sites with increasing biosorbent mass [31].
Experimental equilibrium adsorption data were accessed using the nonlinear forms of Langmuir, Freundlich, and Dubinin–Radushkevich isotherm models. Table 5 shows the parameters of the isotherm models and their respective correlation coefficients (R2).
Based on the correlation coefficient shown, for all Raw-AC dose values, the nonlinear Langmuir isotherm model showed a better fit to the adsorption data than the Freundlich and Dubinin–Radushkevich isotherm models. The maximum adsorption capacities (qmax) were 53.7 mg/g, 53.5 mg/g, and 50.1 mg/g for 5 g/L, 15 g/L, and 20 g/L of Raw-AC, respectively. The decrease in the adsorption amount with increasing biosorbent concentration has been reported in various investigations, which can be attributed to the declining total biosorbent surface area caused by the aggregation of sorption sites [41].
At biosorbent concentrations of 5 g/L and 15 g/L, experimental adsorption isotherms of AC-OH were better fitted to the Langmuir and Dubinin–Radushkevich models, whereas at a higher biosorbent concentration (20 g/L), the biosorption data were better fitted using the Freundlich and Dubinin–Radushkevich models.

2.3.3. Effect of Contact Time

Figure 7a,b show the uptake of Pb(II) versus contact time with Raw-AC and AC-OH, respectively. It was observed that for all initial Pb(II) concentrations ranging from 25 mg/L to 250 mg/L, between 80 and 85% of Pb(II) was removed in the first 10 min of contact time. Following this time, the Pb(II) removal rate became negligible, and equilibrium was achieved in 30 min for the biosorption of Pb(II) by both biosorbents. The rapid uptake of lead ions in the first stage, which is commonly observed for biosorption of metal ions, is due to physicochemical interactions between the metal solution and available functional groups on the biomass surface [42]. As can be seen from Figure 7a,b, the equilibrium time of the biosorption process was 30 min, and after this time, the insignificant removal rate of Pb(II) could be attributed to the saturation of the available sites on the Raw-AC and AC-OH biosorbents surfaces [43].
Table 6 shows the values of kinetic parameters of Pb(II) biosorption on Raw-AC and AC-OH biosorbents obtained from the nonlinear pseudo-first- (PFO) and pseudo-second-order (PSO) models (non-linear equations of PFO and PSO are shown in Supplementary Material).
Comparing the values of the determination coefficient (R2) and the qe,calc obtained from both kinetic models, it can be observed that for all initial concentrations (Ci(Pb(II) = 25–250 mg/L), the nonlinear PSO model fit better than the PFO model. Furthermore, the PSO rate constants (k2) were found to decrease from 0.084–0.484 to 0.024–0.148 (g/mg min) for Raw-AC and from 0.488–3.175 to 0.022–0.032 (g/mg min) for AC-OH, for an increase in the concentration of Pb(II) from 25 to 250 mg/L. Biomass treated with NaOH showed a higher uptake of Pb(II) and biosorption rate k2 compared with the raw biomass. The enhancement of biosorption capacity of treated Ardisia compressa K. leaves was also observed in other biosorbents [32,44].
As shown in Table 6, the regression coefficients obtained from the nonlinear form of the PSO and PSO models were higher than 0.941; furthermore, the qe,cal obtained by both kinetic models were similar to qe,exp. Therefore, the comparison of R2 and qe,cal resulted in inadequate criteria for defining the best-fitting kinetic model. However, the values calculated by the six function errors for all initial concentrations of Pb(II) resulted in lower PSO than the PFO (Table 7), confirming that the PSO was the best model to fit the kinetic data. This result suggests that the removal of Pb(II) was controlled by chemisorption, which involved the strong surface complexation of metal ions with the functional groups on the surface of biosorbents [31].

2.3.4. Temperature Effect on Sorption Capacity

The study of the temperature effect on the sorption of Pb(II) was evaluated using adsorption isotherm experiments by varying the temperature from 300.15 to 330.15 K. Figure 8 shows the adsorption isotherms for Raw-AC and AC-OH at T = 300.15, 315.15, and 330.15 K. It can be observed that the adsorption capacity of Pb(II) of Raw-AC and AC-OH was higher at room temperature compared with that at 315.15 and 330.15 K, confirming that the adsorption was an exothermic process. The decrease in adsorption capacity with temperature can be explained by the breaking of adsorption forces between the metal ions and active sites on the biosorbents caused by the excess of energy supplied to the system, which promoted the desorption of metal ions from surface biosorbent [45,46]. The exothermic adsorption of Pb(II) ions using various types of sorbents, such as Azadirachta indica [47], montmorillonite [45], rice husk [48], and activated tea waste [49], was previously reported.
The isotherm parameters were calculated using the nonlinear equations of Langmuir, Freundlich, and Dubinin–Radushkevich isotherm models.
As shown in Table 8, the adsorption of Pb(II) on AC-OH on the surface of different temperatures studied showed a best fitting to the Langmuir model, as indicated by the high correlation coefficient (R2 = 0.959–0.990) when the temperature increased from 300.15 K to 330.15 K, the Langmuir constant Qm of AC-OH, which indicates the monolayer saturation at equilibrium, decreased from 171.0 to 45.3 mg/g. In the case of Raw-AC, the adsorption of Pb(II) at ambient temperature showed a good fit to the Langmuir model, whereas at T = 313.15 and 330.15 K, it was best fitted to the Freundlich model and the values of KF and n parameters decreased with the temperature rise. At all temperatures studied, the values of n parameters were between 1 and 10, indicating that AC-OH and Raw-AC favorably adsorb Pb(II) ions.
Error functions for all temperatures studied were calculated. Table 9 shows that for AC-OH, the Langmuir isotherms exhibit lower values of error functions for all temperatures studied and is a better fit compared with the Freundlich isotherm.

2.4. Adsorption and Desorption Study

Figure 9a and Figure 9b show the adsorption and desorption cycles of Pb(II) on Raw-AC and AC-OH, respectively. It can be seen that after the three cycles, the percentage of Pb(II) removal on Raw-AC and AC-OH decreased from 80.82% to 45.70% and from 93.80% to 47.05%, respectively. Similarly, the Pb(II) desorption decreased from 67.75 to 45.70% and from 46.94% to 32.25% for Raw-AC and AC-OH, respectively. The decrease in the performance of adsorption and desorption of Raw-AC and AC-OH biosorbents was previously reported in other biosorbents, which was attributed to the possible remanent of metal ions on the surface of the biosorbent after the desorption step and the partial destruction of active functional groups by HCl after each regeneration cycle [22]. Despite the reduction in the percentage of Pb(II) removal after three cycles, both biosorbents have still shown efficient removal and desorption of Pb(II) after three times of recycling. As such, Raw-AC and AC-OH can be considered suitable recyclable biosorbents.

2.5. Comparison of Natural and Alkali Ardisia Compressa K. with Other Biosorbents

In this study, the maximum Pb(II) biosorption capacity, according to Langmuir’s model, was 96.4 and 170.9 mg/g using Raw-AC and AC-OH, respectively. As shown in Table 10, the results obtained in this work are within the usual values, and in some cases, they are between the highest maximum biosorption capacities for other similar biosorbents reported in the scientific literature, indicating the potential for its application in the removal of lead, and perhaps other heavy metals too, from contaminated effluents.

2.6. Proposed Mechanism of Interaction of Pb2+ with Raw-AC and AC-OH

The mechanism of interaction of Pb2+ with Raw-AC and AC-OH could be represented as shown in Figure 10 below:
According to the FTIR results, both biomasses (Raw-AC and AC-OH) present, OH-,-COOH, and NH2 could be complexed with Pb2+ species, or some ion exchange could occur. Adjusting the pH to 4–6, the COOH groups of carboxylic acid release H+ into the solution. This pH adjustment helps the complexation or electrostatic attraction of Pb2+ with both Raw-AC and AC-OH biomasses.

2.7. Data-Driven Optimization

An optimization study was conducted for the two materials (Raw-AC and AC-OH) and its objective was to find which type of material, along with its multivariate combination of initial concentration of Pb, mass, temperature, pH of the solution, and contact time, could provide the maximum qe. However, optimization using the experimentation data required a couple of steps which are mentioned herewith:
  • In the first step: the original data was arranged in the form of a database (see Table 11), where all the tuning variables and the performance indicators were placed together. The database contained a total of 178 experimental points. Bringing the data in such a format would help in the development of an empirical model [61]. It was necessary to develop an empirical model because the optimization algorithms required a direct correlation between the tuning variables and the performance indicator. Thus, it was also necessary to understand the data through the heatmap of the Pearson coefficient of correlation (see Table 12) [62]. It was noted that the initial concentration of Pb was the variable with the highest level of sensitivity for qe, and it was also noted that material 2 had a relatively higher tendency for higher values of qe. The temperature and the pH of the solution were the least sensitive.
2.
In the second step, an empirical model was developed for the selected database. Such a model was developed through the application of artificial neural networks for regression models. The MATLAB environment using the nftool box was implemented. All the input variables were placed in the input layer, and the performance indicator was placed in the performance indicator. A backpropagation method called Bayesian regularization backpropagation was implemented, which was suitable for the noisy database as the origin was experimentation [63]. The training, testing, and validation percentages were set to be 70, 15, and 15, respectively. The number of hidden neurons was iterated and a total of eight neurons came out to be optimal for the minimum mean square error. The regression fit and the error histogram are displayed in Figure 11. During the training, testing, and total phase, the values of R came out to be 0.99276, 0.977, and 0.9905, respectively, which indicates a high goodness of fit. The error histogram also fulfills the normality assumption of errors.
3.
Once the empirical model was developed, in the last step, an optimization study could be conducted. The optimization study was conducted to maximize qe for the given range of each of the tuning variables. The genetic algorithm was implemented in the MATLAB environment through its Optimization toolbox. All the generic configuration of the algorithm was taken to be default [64]. The optimization was conducted two times, one for each material, and the results are shown in Table 13. It is noted that the combination of tuning variables for each type of material was quite similar. For example, for Raw-AC, the optimal combination of temperature, pH of the solution, and contact time came out to be the same, which was 298.15 K, 6, and 1440 min, respectively. The only difference was noted in the cases of initial concentration of Pb and mass, which were 854.16 mg/L and 0.1 g for Raw-AC and 1012.98 mg/L and 0.05 g for AC-OH, respectively. It is quite interesting that even though a couple of variables were the same, the value of optimal qe was quite different. For the combination of Raw-AC and AC-OH, the optimal qe values came out to be 62.287 mg/g and 147.475 mg/g, respectively. It is remarkable how doing such a treatment can improve the results by 57.76%. It is also to be stressed here that the optimal point evaluated through the computational method was placed back into the experimental conditions and conformity between the optimal point through the computational method and the experimentation was met.

3. Materials and Methods

3.1. Pb standard Solutions

Stock solutions (1000 mg/L) of Pb(II) were prepared by dissolving 0.337 g of PbCl2 (99%, Sigma Aldrich, St. Louis, MO, USA) in deionized water. Solutions with 25 to 700 mg/L concentrations were prepared by diluting the stock solutions using deionized water. Pb(II) calibration curves were obtained by diluting 1000 mg/L standard solutions of Pb in 2% v/v HNO3 (Fluka Analytical, St. Louis, MO, USA).

3.2. Biosorbents

Leaves of A. compressa K. were manually collected from the experimental garden at Universidad Tecnológica de Xicotepec de Juárez, located in Xicotepec de Juárez, Puebla (−97.96 20° 16′ 33′′ N, 97° 57′ 36′′ W). Fresh leaves of A. compressa K. were washed, disinfected, and air-dried. The dry material was ground in a blender until a homogeneous fine powder (particle size between 0.42 and 0.80 mm) was obtained. The powder was preserved until use at room temperature in hermetically sealed plastic bags in the absence of light and humidity.
Alkali treatment of raw A. compressa K. (Raw-AC) was done as follows: 10 g of pulverized Raw-AC was added to 250 mL of 1.0 M NaOH in an Erlenmeyer flask (500 mL) and shaken at 140 rpm for 2 h. Then, the sample was filtered under a vacuum and rinsed several times using deionized water until the wash solution pH reached approximately 6.5. The treated biomass labeled AC-OH was air-dried and stored in glass bottles. Figure 12 illustrates the preparation procedure of the biosorbents.

3.3. Physicochemical Analysis

Association of Analytical Communities (AOAC (2007)) methods were used for the chemical characterization of A. compressa leaves [65]: ash, moisture, raw fiber, and ethereal extract were found using the Soxhlet method; protein was found using the Kjeldahl method and nitrogen-free extract (NFE) was calculated using the percentage differences. The total soluble solids (TSSs) were identified using a digital refractometer (PR-101ATAGO PALETTE) according to the method previously described [65]. All determinations were done in triplicate.

3.4. Characterization Techniques

The pHPZC was obtained as previously described [32]. Samples of Raw-AC and AC-OH, before and after contact with metal ions, were characterized using a Fourier transform infrared spectrometer (Nicolet Nexus 670) to identify the functional groups on the biomass surface. Surface characteristics of Raw-AC and AC-OH biosorbents before and after the uptake of Pb(II) were studied using scanning electron microscopy (JEOL JSM-IT300). An energy-dispersive X-ray spectrometer was used to determine the approximate chemical composition on the surface of Raw-AC and AC-OH biosorbents.

3.5. Biosorption Study

In this work, the biosorption process was carried out using a batch technique. For the kinetic study, 0.1 g of Raw-AC and AC-OH was mixed with 10 mL of Pb(II) solutions at initial concentrations from 25 mg/L to 250 mg/L. The samples were shaken at 140 rpm in an orbital shaker (CRP-0228, Scientific) for times ranging from 15 min to 1440 min. After each contact time, the samples were centrifuged (CRM Globe, Certificient, Chicago, IL, USA) for 5 min, and the Pb(II) contents in the aqueous solutions were determined using flame atomic absorption spectrometry (iCe Serie TermoScientific).
After each contact time, the amount of Pb(II) adsorbed on the surface of Raw-AC and AC-OH was calculated using Equation (1):
q t = C i C t m · V  
where Ci and Ct are, respectively, the initial and final concentrations of Pb(II) (mg/L); V (L) is the volume of solution; and m (g) is the mass of biosorbents.
In this study, the effects of the solution pH, dose of the biosorbents, and temperature were carried out by varying the initial lead concentration from 25 to 1000 mg/L. For the kinetic study, the temperature and solution pH were fixed, whereas the initial lead concentration was varied from 25 to 250 mg/L and the contact time was changed from 5 to 1440 min.
Table 14 gives the experimental conditions used to investigate the effects of contact times, solution pH, temperature, and dose of biosorbents on the removal of Pb(II).
All experiments were performed in duplicate and the results were expressed as averaged values. The Supplementary Materials provide the kinetic and isotherm models, as well as the error functions analysis used in this study.

3.6. Kinetic Models

This study employed the nonlinear equations of pseudo-first- and pseudo-second-order models (Equation (2) and Equation (3), respectively) to investigate the kinetics of Pb(II) biosorption onto Raw-AC and AC-OH:
q t = q e 1 e x p ( k 1 t )
q t = k 2 q e 2 t 1 + k 2 q e t
where qe is the theoretical adsorption capacity (mg/g), and k1 (1/min) and k2 (g/mg min) are the pseudo-first- and pseudo-second-order rate constants, respectively.

3.7. Isotherm Models

Experimental data were examined using Langmuir, Freundlich, and Dubinin-Radushkevich (D-R) isotherm models.
Equation (4) describes the non-linear form of the Langmuir isotherm model:
q e = q m K L C e 1 + K L C e  
where qm (mg/g) is the maximum sorption capacity, and KL (L/mg) is the Langmuir equilibrium constant, which indicates the affinity of the sorbate for the solute [55].
The Langmuir model assumes that adsorption takes place for monolayer adsorption of the adsorbate from a liquid solution on a surface of biosorbent containing a finite number of identical sites and all adsorption sites have equal adsorption energies [55,66].
The Freundlich model is an empirical isotherm that can be used for non-ideal adsorption, which is mostly used to understand the adsorption of metal ions on a heterogeneous surface with multilayer adsorption. It can also define an exponential distribution of active sites and their energy [54]. The non-linear form of the Freundlich isotherm model is expressed as Equation (5):
q e = K F C e 1 / n  
where KF (mg/g)(L/mg)1/n and n are the Freundlich constants associated with the adsorption capacity and adsorption intensity of the adsorbent, respectively. Ce (mg/L) is the adsorbate equilibrium concentration. When n = 1, the isotherm is linear and indicates that all sites on the adsorbent have equal affinity for the adsorbates. Values of n > 1 indicate the affinities decreased with increasing adsorption density [54]. The greater the value of n, the more favorable the adsorption and the more heterogeneous the surface of the particles will be [67].
The D-R isotherm is an empirical model that is generally employed to find whether the adsorption involved in the experimental data is physical or chemical [68]. The non-linear form of the D-R isotherm model is shown in the following Equation (6):
q e = q m e β ϵ 2  
where β (mol2/kJ2) is a constant related to adsorption energy, ε = R T l n ( 1 + 1 C e ) is the adsorption potential (kJ mol−1), R (8.314 J mol−1 K−1) is the universal gas constant, T (K) is the absolute temperature, and E = 1 2 β is the adsorption energy (kJ/mol).
The numerical value from the free energy of the molecule (E) gives an indication of the nature of the interaction forces between lead ions and the active sites on the composite surface. When the value of the adsorption energy was less than 8 kJ/mol, it indicates that the adsorption occurred physically; if it was between 8 and 16 kJ/mol, it suggests that the adsorption process was carried out chemically, driven by the ion exchange mechanism; and chemisorption was observed when E values are between 20 and 40 kJ/mol [69].

3.8. Adsorption–Desorption Cycles

Experiments of adsorption and desorption cycles were conducted: 10 g/L of Raw-AC and AC-OH were mixed with 1000 mg/L of Pb(II) for 1440 min at room temperature and solution pH at 6. The samples were filtered, and the adsorption efficiency was obtained utilizing Equation (7):
A d s o r p t i o n   e f f i c i e n c y   % = C a d s C i n i t i a l × 100  
After the adsorption process, the biosorbents were dried and weighed; then, the desorption experiments were conducted by mixing the biosorbents at ambient temperature for 2 h with 0.5 M HCl. The Pb(II) concentrations in each solution were measured, and the desorption efficiency was obtained utilizing Equation (8):
D e s o r p t i o n   e f f i c i e n c y   % = C d e s C a d s × 100  
where Cdes is the concentration of Pb(II) desorbed in mg/g and Cads is the concentration of Pb(II) adsorbed in mg/g.
After desorption, the samples were rinsed several times with deionized water to remove the eluent agent from the biosorbents. The samples were then dried and weighed for further reuse. In this study, three adsorption and desorption cycles were repeated.

3.9. Framework of Empirical Model and Optimization Process

Owing to the complexity of the involvement of so many tuning variables, it is not easy to determine the optimal set conditions for this problem. For this purpose, an artificial intelligence method consisting of the artificial neural network was adapted for the empirical modeling, and later on, a genetic algorithm was applied for optimization purposes, which would eventually give out the best combination of all the multivariate tuning variables [70].

4. Conclusions

In conclusion, this study demonstrates that Ardisia compressa K. leaves, particularly those treated with a solution of 1M NaOH (AC-OH), exhibit a higher sorption capacity for Pb(II) from aqueous solutions compared with natural Ardisia compressa K. leaves (Raw-AC). The surface modification of the biosorbent after the alkali treatment was confirmed via pHPZC and FTIR analysis, which revealed the presence of carboxyl, hydroxyl, and amino groups responsible for Pb(II) binding.
The removal of Pb(II) was found to be dependent on various factors, including solution pH, contact time, biosorbent dose, and water temperature. The optimum experimental conditions for maximum Pb(II) removal by both biosorbents were at pH 6 and T = 300.15 K.
The kinetic data analysis indicated that the pseudo-second-order kinetic model best described Pb(II) biosorption on both Raw-AC and AC-OH, which suggests that chemisorption controlled the rate of reaction. The Langmuir isotherm model described the adsorption isotherms for both biosorbents at different solution pH values well, suggesting monolayer sorption on a homogeneous surface took place. Furthermore, the study introduced the application of artificial neural networks and genetic algorithms for regression modeling and optimization purposes.
The model showed high reliability, and the optimization study revealed a significant improvement of around 57.76% in the indicator “qe” for AC-OH. The optimal conditions for AC-OH were determined as follows: initial concentration of Pb: 1012.98 mg/L, mass: 0.05 g, temperature: 298.15 K, pH of the solution: 6, and contact time: 1440 min, resulting in an optimal qe of 147.475 mg/g. In summary, the results indicate that Ardisia compressa K. leaves can serve as a promising, cost-effective, and efficient biosorbent for removing Pb(II) ions from aqueous solutions. The study also highlights the potential of artificial neural networks and genetic algorithms for optimizing biosorption processes. These findings contribute to the development of environmentally friendly and sustainable methods for heavy metal removal from water sources.
A significant finding of this study pertains to the coefficient of determination, which indicated that the Dubinin–Radushkevich isotherm model exhibited lower values compared with the Langmuir and Freundlich, suggesting a need for further investigation into the applicability and parameter-based assessment of the Dubinin–Radushkevich model to elucidate sorption mechanisms.
The insights from this research hold valuable implications for engineering education, as it showcases how modifying biosorbents, optimizing process conditions, employing kinetic and isotherm models, and utilizing advanced techniques like artificial neural networks and genetic algorithms can be integrated into engineering curricula to foster a comprehensive understanding of designing effective and eco-friendly solutions for heavy metal removal in water treatment systems. The social insights derived from this research underscore the potential impact of innovative engineering approaches on addressing environmental challenges, demonstrating the significance of interdisciplinary collaboration between engineering and environmental sciences to develop sustainable solutions for water pollution, thereby imparting the importance of considering broader societal and ecological implications of technological advancements in engineering education.

Supplementary Materials

The following supporting information can be downloaded from https://www.mdpi.com/article/10.3390/molecules28176387/s1. Error functions analysis.

Author Contributions

A.Y.V.-S., M.A. and A.A.S. conceived and planned the experiments; A.A.S., C.A. and I.A. contributed to the characterization of the samples. M.A., R.T. and A.R.V.-O. wrote the manuscript with input from all authors. E.C.L., M.A. and I.A. contributed to the interpretation of the results. All authors provided critical feedback and helped to shape the research, analysis, and manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

The authors are grateful to Adriana Tejeda Cruz and Eliezer Hernández Me-cinas for their assistance in the X-ray diffraction and FTIR measurements.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Not applicable.

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Figure 1. pHinitial vs. pHfinal of Raw-AC and AC-OH biosorbents.
Figure 1. pHinitial vs. pHfinal of Raw-AC and AC-OH biosorbents.
Molecules 28 06387 g001
Figure 2. SEM images and EDS analysis of RAW-AC (left) and RAW-AC--Pb (right); in the zoomed-in image, the red dots represent the Pb(II) on the surface of the sample.
Figure 2. SEM images and EDS analysis of RAW-AC (left) and RAW-AC--Pb (right); in the zoomed-in image, the red dots represent the Pb(II) on the surface of the sample.
Molecules 28 06387 g002
Figure 3. SEM images and EDS analysis of AC-OH (left) and AC-OH-Pb (right); in the zoomed-in image, the red dots represent the Pb(II) on the surface of the sample.
Figure 3. SEM images and EDS analysis of AC-OH (left) and AC-OH-Pb (right); in the zoomed-in image, the red dots represent the Pb(II) on the surface of the sample.
Molecules 28 06387 g003
Figure 4. FTIR spectra of (a) Raw-AC and Raw-AC-Pb and (b) AC-OH and AC-OH-Pb.
Figure 4. FTIR spectra of (a) Raw-AC and Raw-AC-Pb and (b) AC-OH and AC-OH-Pb.
Molecules 28 06387 g004
Figure 5. Adsorption isotherms of Pb(II) on Raw-AC and AC-OH at pH = 2 (a,b), pH = 4 (c,d), and pH = 6 (e,f).
Figure 5. Adsorption isotherms of Pb(II) on Raw-AC and AC-OH at pH = 2 (a,b), pH = 4 (c,d), and pH = 6 (e,f).
Molecules 28 06387 g005
Figure 6. Adsorption isotherms of Pb(II) on Raw-AC and AC-OH at doses of 5 g/L (a,b), 15 g/L (c,d), and 20 g/L (e,f).
Figure 6. Adsorption isotherms of Pb(II) on Raw-AC and AC-OH at doses of 5 g/L (a,b), 15 g/L (c,d), and 20 g/L (e,f).
Molecules 28 06387 g006aMolecules 28 06387 g006b
Figure 7. qe (mg/g) vs. contact time t (min) of (a) Raw-AC and (b) AC-OH.
Figure 7. qe (mg/g) vs. contact time t (min) of (a) Raw-AC and (b) AC-OH.
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Figure 8. Adsorption isotherms of Pb(II) on Raw-AC and AC-OH at temperatures 300.15 (a,b), 313.15 (c,d), and 330.15 K (e,f).
Figure 8. Adsorption isotherms of Pb(II) on Raw-AC and AC-OH at temperatures 300.15 (a,b), 313.15 (c,d), and 330.15 K (e,f).
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Figure 9. Adsorption and desorption cycles of Pb(II) with (a) Raw-AC and (b) AC-OH biosorbents.
Figure 9. Adsorption and desorption cycles of Pb(II) with (a) Raw-AC and (b) AC-OH biosorbents.
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Figure 10. Interaction mechanism of the uptake of Pb2+ with raw-AC and AC-OH.
Figure 10. Interaction mechanism of the uptake of Pb2+ with raw-AC and AC-OH.
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Figure 11. (Left) Results of empirical modeling through a comparison between experimental and simulated qe. (Right) Histogram of the errors between the experimental and simulated qe values.
Figure 11. (Left) Results of empirical modeling through a comparison between experimental and simulated qe. (Right) Histogram of the errors between the experimental and simulated qe values.
Molecules 28 06387 g011
Figure 12. Schematic representation of the preparation of the biosorbents.
Figure 12. Schematic representation of the preparation of the biosorbents.
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Table 1. Physicochemical parameters of Ardisia compressa K. leaves.
Table 1. Physicochemical parameters of Ardisia compressa K. leaves.
ParameterPercent Composition (% w/w)
Total soluble solids (%)86.49 ± 0.12
Moisture (%)13.51 ± 0.12
Ash (%)6.74 ± 0.01
Ethereal extract (%)
Raw fiber (%)
Protein (%)
3.60 ± 0.29
16.51 ± 0.34
5.83 ± 0.12
Nitrogen-free extract (%)53.80 ± 0.36
All values are reported in % on a dry weight basis.
Table 2. Comparison of pHPZC values of untreated and alkaline treated biosorbents.
Table 2. Comparison of pHPZC values of untreated and alkaline treated biosorbents.
BiosorbentpHPZC
(Raw Biosorbent)
pHPZC
(Alkali-Treated Biosorbent)
Ref.
Prunus armeniaca L. shells4.95.7[31]
Leucaena leucephala leaves6.77.2[32]
Cupressus sempervirens
Carob shells
Nostoc commune
6.1
5.4
1.3
6.7
6.52
2.5
[33]
[34]
[28]
Ardisia compressa K. 4.86.4This study
Table 3. Nonlinear Langmuir, Freundlich, and Dubinin–Radushkevich isotherm parameters for Pb(II) biosorption on Raw-AC and AC-OH biomass at solution pH = 2, 4, and 6.
Table 3. Nonlinear Langmuir, Freundlich, and Dubinin–Radushkevich isotherm parameters for Pb(II) biosorption on Raw-AC and AC-OH biomass at solution pH = 2, 4, and 6.
pHModelParametersRaw-ACAC-OH
2LangmuirQmax (mg/g)26.443.7
KL·10−2 (L/mg)2.00159.431
R20.9810.971
FreundlichKF (mg/g)(L/mg)1/n3.58016.226
n3.2005.404
R20.9600.924
Dubinin–Radushkevich (D-R)Qmax (mg/g)21.94841.965
β (mol2/kJ2)93.5930.242
E (kJ/mol)0.0731.437
R20.8970.917
4LangmuirQmax (mg/g)48.169.41
KL·10−2 (L/mg)0.88256.634
R20.9920.984
FreundlichKF (mg/g)(L/mg)1/n2.22923.975
n2.0844.979
R20.9700.913
Dubinin–Radushkevich (D-R)Qmax (mg/g)34.18362.050
β (mol2/kJ2)413.0060.100
E (kJ/mol)0.0352.236
R20.9320.867
6LangmuirQmax (mg/g)96.4171.0
KL·10−2 (L/mg)0.7819.076
R20.9970.990
FreundlichKF (mg/g)(L/mg)1/n2.65422.311
n1.7102.043
R20.9920.976
Dubinin–Radushkevich (D-R)Qmax (mg/g)55.216120.205
β (mol2/kJ2)239.3832.729
E (kJ/mol)0.0460.428
R20.9100.913
Table 4. Error function values of the Langmuir, Freundlich, and Dubinin–Radushkevich isotherm models at solution pH = 2, 4, and 6.
Table 4. Error function values of the Langmuir, Freundlich, and Dubinin–Radushkevich isotherm models at solution pH = 2, 4, and 6.
BiosorbentpHModelError Functions
APESSE∆q(%)χ2EABSRMSE
Raw-AC2Langmuir9.9344.70319.2011.7905.8980.970
Freundlich16.26121.03519.8811.58110.6042.051
D-R36.48351.89657.739353.99215.8993.222
4Langmuir12.0518.05417.5131.2235.8751.269
Freundlich19.73436.16423.8402.18013.9222.689
D-R47.70681.30770.448509.59921.1964.033
6Langmuir16.7869.11930.3253.1336.7211.510
Freundlich17.54525.42729.1711.51612.6952.255
D-R53.582272.07072.248903.79341.2737.377
AC-OH2Langmuir6.40254.6958.4533.00914.6173.307
Freundlich17.359142.97824.8697.25328.2745.347
D-R30.443156.43647.782911.67230.0735.593
4Langmuir24.35987.29630.82110.18419.8234.178
Freundlich68.640469.13443.90216.67552.8719.686
D-R38.773719.03653.67151.39254.90911.992
6Langmuir16.701169.56921.7844.10925.3635.824
Freundlich81.765402.405131.18416.08448.8178.971
D-R55.1641427.99671.002427.18088.15716.900
Table 5. Nonlinear Langmuir, Freundlich, and Dubinin–Radushkevich isotherm parameters for Pb(II) biosorption on Raw-AC and AC-OH biomass at dose = 5 g/L, 15 g/L, and 20 g/L.
Table 5. Nonlinear Langmuir, Freundlich, and Dubinin–Radushkevich isotherm parameters for Pb(II) biosorption on Raw-AC and AC-OH biomass at dose = 5 g/L, 15 g/L, and 20 g/L.
Dose (g/L)ModelParametersRaw-ACAC-OH
5LangmuirQmax (mg/g)53.773.7
KL·10−2 (L/mg)2.1050.773
R20.9960.957
FreundlichKF (mg/g)(L/mg)1/n4.90523.916
n2.4944.414
R20.9530.953
Dubinin–Radushkevich (D-R)Qmax (mg/g)34.77187.074
β (mol2/kJ2)68.94281.735
E (kJ/mol)0.0850.078
R20.9080.836
15LangmuirQmax (mg/g)53.553.3
KL·10−2 (L/mg)0.613128.915
R20.9960.966
FreundlichKF (mg/g)(L/mg)1/n0.95224.446
n1.5392.829
R20.9860.964
Dubinin–Radushkevich (D-R)Qmax (mg/g)29.30347.476
β (mol2/kJ2)310.5920.136
E (kJ/mol)0.0401.916
R20.9140.905
20LangmuirQmax (mg/g)50.190.6
KL·10−2 (L/mg)0.80130.554
R20.9980.993
FreundlichKF (mg/g)(L/mg)1/n0.94120.674
n1.4721.395
R20.9890.997
Dubinin–Radushkevich (D-R)Qmax (mg/g)25.70642.859
β (mol2/kJ2)157.1440.212
E (kJ/mol)0.0561.537
R20.9550.951
Table 6. Parameter values calculated using the nonlinear forms of the pseudo-first-order and pseudo-second-order kinetic models for Pb(II) biosorption on Raw-AC and AC-OH biomass at Ci = 25 mg/L, 50 mg/L, 100 mg/L, and 250 mg/L.
Table 6. Parameter values calculated using the nonlinear forms of the pseudo-first-order and pseudo-second-order kinetic models for Pb(II) biosorption on Raw-AC and AC-OH biomass at Ci = 25 mg/L, 50 mg/L, 100 mg/L, and 250 mg/L.
BiosorbentCi
(mg/L)
Pseudo-First-OrderPseudo-Second-Order
qe,cal
(mg/g)
k1
(1/min)
R2qe,cal
(mg/g)
k2
(g/mg min)
R2
Raw-AC252.40.3410.9762.40.9700.994
506.00.1180.9856.20.0380.987
10011.70.2280.94111.90.0580.973
25016.70.3320.99016.70.1480.991
AC-OH253.20.4090.9993.23.1750.999
506.70.2980.9996.80.7280.999
10013.60.2320.99913.70.1530.999
25034.50.2000.99734.80.0321.000
Table 7. Error functions of the PFO and PSO kinetic models.
Table 7. Error functions of the PFO and PSO kinetic models.
BiosorbentCi
(mg/L)
ModelError Functions
ARESSE
(10−2)
∆q(%)
(10−2)
χ2
(10−2)
EABSRMSE
Raw-AC25PFO1.4861.5312.0990.6350.2510.055
PSO1.2851.0651.7280.4440.2180.046
50PFO1.7589.4752.2181.6330.6980.138
PSO1.7258.1882.1661.5100.6630.128
100
250
PFO2.79099.4823.5778.5052.2520.446
PSO1.71244.8542.4463.8741.3600.300
PFO1.05128.1151.2971.6881.2260.237
PSO0.93326.3591.2531.5831.0890.230
AC-OH25PFO0.3100. 0930.4240.0290.0600.015
PSO0.2980. 0640.3520.0190.0570.013
50PFO0.3180.5520.4950.0820.1280.037
PSO0.2950.4590.4520. 0680.1190.034
100
250
PFO0.1360.4460.2200.0330.1110.033
PSO0.3411.5600.4140.1160.2760.062
PFO0.71146.7370.8891.3551.4670.342
PSO0.2636.9430.3450.2040.5390.132
Table 8. Langmuir, Freundlich, and Dubinin–Radushkevich (D-R) isotherm parameters using nonlinear regression analysis for Pb(II) biosorption on Raw-AC and AC-OH biomass at different temperatures.
Table 8. Langmuir, Freundlich, and Dubinin–Radushkevich (D-R) isotherm parameters using nonlinear regression analysis for Pb(II) biosorption on Raw-AC and AC-OH biomass at different temperatures.
Temperature
(K)
ModelParametersRaw-ACAC-OH
300.15LangmuirQmax (mg/g)96.4171
KL·10−2 (L/mg)0.7819.076
R20.9970.990
FreundlichKF (mg/g)(L/mg)1/n2.65422.311
n1.712.043
R20.9920.976
Dubinin–Radushkevich (D-R)Qmax (mg/g)53.840120.205
β (mol2/kJ2)227.7202.729
E (kJ/mol)0.0470.428
R20.8990.913
313.15LangmuirQmax (mg/g)76.149.6
KL·10−2 (L/mg)0.41742.48
R20.9880.971
FreundlichKF (mg/g)(L/mg)1/n1.37514.096
n1.6714.173
R20.9990.884
Dubinin–Radushkevich (D-R)Qmax (mg/g)38.08147.671
β (mol2/kJ2)264.0460.324
E (kJ/mol)0.0441.243
R20.8650.970
330.15LangmuirQmax (mg/g)92.445.3
KL·10−2 (L/mg)0.23124.844
R20.9810.959
FreundlichKF (mg/g)(L/mg)1/n0.50812.635
n1.3113.329
R20.9850.904
Dubinin–Radushkevich (D-R)Qmax (mg/g)30.87939.923
β (mol2/kJ2)494.1260.503
E (kJ/mol)0.0320.997
R20.9040.887
Table 9. Error function values of the Langmuir, Freundlich, and Dubinin–Radushkevich equilibrium models at 300.15, 313.15, and 330.15 K.
Table 9. Error function values of the Langmuir, Freundlich, and Dubinin–Radushkevich equilibrium models at 300.15, 313.15, and 330.15 K.
BiosorbentT
(K)
ModelError Functions
APESSE∆q(%)χ2EABSRMSE
Raw-AC300.15Langmuir19.5839.1190.3033.1336.7211.350
Freundlich20.02720.9960.2911.40511.5342.049
D-R52.451298.24070.076608.20042.5907.723
313.15Langmuir26.94020.9690.3977.40411.4412.048
Freundlich5.4681.2620.1140.2112.1600.502
D-R52.210244.61367.720210.52335.0966.994
330.15Langmuir23.03516.3900.3053.4049.5841.811
Freundlich18.85812.3750.2421.3107.9471.573
D-R47.87975.58763.68694.23519.8723.888
AC-OH300.15Langmuir16.701169.5690.2184.10925.3635.824
Freundlich81.765402.4051.31216.08448.8178.971
D-R55.1631427.99671.002427.15888.15716.900
313.15Langmuir54.84780.3791.1317.00220.2124.009
Freundlich102.467317.8222.17719.91740.8027.973
D-R37.86597.50357.45478.55723.5684.416
330.15Langmuir18.71384.4800.2443.08820.8394.110
Freundlich71.759196.3371.26113.28435.8606.266
D-R43.927231.23659.70910.93435.3366.801
Table 10. Comparison of Pb(II) adsorption capacity of different sorbents.
Table 10. Comparison of Pb(II) adsorption capacity of different sorbents.
BiosorbentDose
(g/L)
Ci
(mg/L)
pHKinetic ModelMechanismqe,max
(mg·g−1)
Ref.
Moringa oleifera tree leaves420–2005PSOChemisorption34.6[42]
Nostoc commune0.5127- 4424.5–5.5PSOChemisorption384.6[28]
Cystoseira stricta10.5–1.03--65.0[50]
Leucaena leucocephala leaves1010–5006PSOChemisorption25.5[51]
Ceratophyllum demursum0.11.46–1.737-Physical, monolayer44.8[52]
Punica geranatum leaves0.11.46–1.737-Physical, monolayer31.78[53]
Mirabilis jalapa leaves0.150–1254.5-Multimolecular layers38.5[54]
Laurus nobilis leaves waste45–106PFOChemisorption96.1[55]
Cladophora fascicularis2225.4–838.35PSOChemisorption227.7[56]
Nickel ferrite nanoparticle-0.01–0.055PSO-19.2[57]
MoS2/thiol-functionalized multiwalled
carbon nanotube
220–1506PSOMultilayer90.0[58]
Nano Zero-Valent Iron particles0.110–10006PSOChemisorption140.8[59]
Cu-Based Composite Track-Etched Membranes0.0033–0.0052505PSOChemisorption0.44–0.56[60]
Raw-AC1025–10006PSOChemisorption96.4In this study
AC-OH1025–10006PSOChemisorption170.9In this study
Table 11. Format of the database for the development of the empirical model. Note: material 1 refers to the combination of Raw-AC and material 2 refers to the combination of AC-OH.
Table 11. Format of the database for the development of the empirical model. Note: material 1 refers to the combination of Raw-AC and material 2 refers to the combination of AC-OH.
MaterialInitial Concentration of Pb (mg/L)Mass (g)Temperature (K)pH of the SolutionContact Time (min)qe (mg/g)
124.4140.1298.15214402.41213
148.2040.1298.15214404.33674
192.4920.1298.15214407.1832
1412.920.1298.156144034.3227
1531.760.1298.156144041.574
1854.160.1298.156144062.287
226.9580.05298.15214405.36626
244.6130.05298.15214408.84096
289.10.05298.152144017.61704
2333.020.05298.156144063.7672
2757.880.05298.1561440127.848
21012.980.05298.1561440147.475
Table 12. Understanding the correlation coefficient between the tuning and performance indicators through Pearson’s coefficient of correlation.
Table 12. Understanding the correlation coefficient between the tuning and performance indicators through Pearson’s coefficient of correlation.
MaterialInitial Concentration of PbMassTemperaturepH of the SolutionContact Timeqe
Material1.00−0.01−0.240.01−0.010.010.27
Initial concentration of Pb−0.011.000.14−0.02−0.120.270.79
Mass−0.240.141.00−0.060.060.38−0.18
Temperature0.01−0.02−0.061.000.160.22−0.03
pH of the solution−0.01−0.120.060.161.00−0.23−0.03
Contact time0.010.270.380.22−0.231.000.22
qe0.270.79−0.18−0.03−0.030.221.00
Table 13. Optimality of Raw-AC and AC-OH through conformity between the computational method and experimental procedure.
Table 13. Optimality of Raw-AC and AC-OH through conformity between the computational method and experimental procedure.
BiomassInitial Concentration of Pb (mg/L)Mass (g)Temperature (K)pH of the SolutionContact Time (min)Optimal qe (mg/g)
Raw-AC854.160.1298.156144062.287
AC-OH1012.980.05298.1561440147.475
Table 14. Values of contact times, solution pH, temperature, and adsorbent dose parameters used for the experimental process.
Table 14. Values of contact times, solution pH, temperature, and adsorbent dose parameters used for the experimental process.
ExperimentsExperimental Parameters
pHTime (min)Ci (mg/L)Dose (g/L) Temperature (K)
Solution pH2–6144025–100010300.15
Dose6144025–10005–20300.15
Contact times65–144025–25010300.15
Temperature6144025–100010300.15–330.15
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Vázquez-Sánchez, A.Y.; Lima, E.C.; Abatal, M.; Tariq, R.; Santiago, A.A.; Alfonso, I.; Aguilar, C.; Vazquez-Olmos, A.R. Biosorption of Pb(II) Using Natural and Treated Ardisia compressa K. Leaves: Simulation Framework Extended through the Application of Artificial Neural Network and Genetic Algorithm. Molecules 2023, 28, 6387. https://doi.org/10.3390/molecules28176387

AMA Style

Vázquez-Sánchez AY, Lima EC, Abatal M, Tariq R, Santiago AA, Alfonso I, Aguilar C, Vazquez-Olmos AR. Biosorption of Pb(II) Using Natural and Treated Ardisia compressa K. Leaves: Simulation Framework Extended through the Application of Artificial Neural Network and Genetic Algorithm. Molecules. 2023; 28(17):6387. https://doi.org/10.3390/molecules28176387

Chicago/Turabian Style

Vázquez-Sánchez, Alma Y., Eder C. Lima, Mohamed Abatal, Rasikh Tariq, Arlette A. Santiago, Ismeli Alfonso, Claudia Aguilar, and América R. Vazquez-Olmos. 2023. "Biosorption of Pb(II) Using Natural and Treated Ardisia compressa K. Leaves: Simulation Framework Extended through the Application of Artificial Neural Network and Genetic Algorithm" Molecules 28, no. 17: 6387. https://doi.org/10.3390/molecules28176387

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