Preparation and Characterization of Functionalized Cellulose Nanomaterials (CNMs) for Pb(II) Ions Removal fromWastewater

Due to their remarkable properties, cellulose nanomaterials are emerging materials for wastewater (WW) treatment. In this study, both pristine cellulose nanomaterial (CNM) and sodium periodate modified cellulose nanomaterial (NaIO4-CNM) were prepared from the stem of the Erythrina brucei plant for the removal of Pb(II) ions from WW. As-prepared CNMs were characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), scanning electron microscope (SEM), and thermogravimetric analysis with differential thermogravimetry (TGA-DTG) analysis. +e as-prepared and characterized CNMs were tested for the removal of Pb(II) ions from secondary run-off wastewater (SERWW). Langmuir and Freundlich adsorption isotherms were certainly fixed to a maximum Pb(II) ions uptake capability (Qmax) of 91.74 and 384.62mg g by CNM and NaIO4-CNM adsorbents, respectively. +e pseudo-second-order (PSO) kinetics model was well fitted to the uptake process. Results revealed that the percentage removal (%R) of Pb(II) ions was decreased by the presence of nitrogen and organic matter, but not affected by the presence of phosphorous in SERWW. Due to its high efficiency, NaIO4-CNM was selected for the regeneration study. +e regeneration study was conducted after desorption of Pb(II) ions from the adsorbent by the addition of HCl, and the regenerated sorbent was reused as an adsorbent for at least 13 successive cycles. +e results indicated excellent recycling capabilities, and the adsorbent was used as adsorbing material for the removal of Pb(II) ions from SERWW after 13 successive cycles without significant efficient loss.


Introduction
Water is the most important resource for all living things throughout the world [1,2,34]. However, water pollution is considered the greatest stimulating issue all over the world, especially in developing countries like Ethiopia [4][5][6]. e major sources of water pollutions are different industrial activities, urbanization, and population growth. Among these, different industries release several toxic contaminants such as heavy metals, organic dyes, pharmaceuticals, petroleum products, and others into water bodies [7][8][9]. Owing to their noxiousness and bioaccumulation, they provide enormous hazards to living things [10][11][12]. Among these pollutants, the contamination of water with heavy metals is a severe cause of environmental and human health problems [13][14][15].
is is because they are nonbiodegradable and can be stored in living tissues for a long time relative to organic pollutants [16,17]. Some of these heavy metals are As, Pb, Hg, Cd, Cr, Cu, Ni, Ag, and Zn. Water bodies with high concentrations of these metals can cause severe damage to human health and aquatic animals. For instance, the presence of high concentrations of Pb in the environment causes hazardous toxicity to the reproductive systems that harms the brain, liver, and kidney of human beings and aquatic living things [18]. Furthermore, based on the toxicological studies on nephrotoxicity, exposure to Pb(II) ions can be related to renal tubular necrosis, and exposure to Pb is directly related to the failure of glomeruli [19]. As a result of this, the preparation of green and biodegradable CNMs to remove Pb(II) ions from SERWW before its release into the different environments is very necessary [20]. erefore, a number of technologies were tested for the removal of Pb(II) ions from wastewater, including precipitation, filtration, reverse osmosis, solvent extraction, ion exchange, coagulation, and adsorption [21]. However, most of these technologies require a high price, show low removal abilities, and require additional energy to purify wastewater [22]. From all of these, adsorption is selected because it is simple, is relatively cheap, removes pollutants at ppm levels, is highly efficient, and has abundant adsorbent materials such as activated carbon, carbon nanotubes (CNT), composites, and nanoparticles [23][24][25]. Among these adsorbent materials, polymeric materials such as cellulose, chitin, chitosan, gelatin, alginate, and starch have been selected currently for the removal of toxic metals from aqueous media, due to the cost-friendly and easy recycling of adsorbent materials [26].
Among these, cellulose-based materials have improved merits of being easily available, nonpoisonous, and renewable and having plenty of accessible hydroxyl functional groups which are very active for different chemical modification systems [27][28][29][30][31]. In spite of its pronounced properties, the demerits of cellulose-based materials in wastewater decontamination are its low hydrophilicity, physical and chemical stability, and removal capacity [32].
is shortcoming was easily improved by disintegrating cellulose into cellulose nanomaterials (CNMs) [33]. CNMs are biodegradable materials with at least one dimension in a nanometer (nm) scale. is material was prepared by disintegrating cellulose into CNMs through the addition of sulfuric acid, and the as-prepared CNMs show pronounced properties such as high surface area, small particle size, high mechanical strength, and chemical stability [34]. Depending on the preparation methods and source materials, CNMs can be classified into cellulose nanofibers (CNFs), cellulose nanocrystals (CNCs), and bacterial cellulose [35]. Among these, the study was focused on cellulose nanocrystals (CNCs) prepared from the stem of renewable and biodegradable Ethiopian indigenous Erythrina brucei plants.
To show the novelty of the study, the authors reviewed a number of studies that have been performed previously on the CNM-based adsorbents prepared from different polymeric materials such as sugarcane bagasse [36], date palm (Phoenix dactylifera L.), [37], Cotton residue [38], banana [39], corn husk [40], and Millettia ferruginea plant (Ethiopian indigenous plants) [41]. As per the knowledge of the authors, no work has been reported on the CNM sorbents prepared from the stem of Ethiopian indigenous Erythrina brucei plants (Korch in Amharic, Walensu in Afaan Oromo, Boro in Ganta). In addition, the stem of the Erythrina brucei plant in Ethiopia does not have significant functions and is left as waste material. erefore, it does not influence Ethiopian economic security and is used as a low-cost adsorbent in this study. Furthermore, the majority of research reported the removal of Pb(II) ions from synthetic wastewater only, but there was a big gap found in the studies reporting the removal of Pb(II) ions from real wastewater. erefore, this study was focused on the preparation and characterization of both CNM and NaIO4-CNM sorbent materials prepared from the stem of locally available Ethiopian indigenous Erythrina brucei plants for the removal of Pb(II) ions from real WW.

Experimental Procedures.
e physicochemical property measurements of SERWW were performed and presented in Table 1. e stock solution of Pb(II) ions was prepared by taking a 1000 mL volumetric flask and adding the required amount in 1 g of Pb(NO 3 ) 2 into the flask. en, to this flask, a certain volume of distilled water was added. e added components were carefully mixed in the form of a solution. Finally, distilled water was added up to the mark of the flask with the help of a micropipette. e diluted solutions were prepared by taking suitable volume from the previously prepared stock solution and adding it to 100 mL volumetric flasks. To these flasks, distilled water was carefully added up to the mark. Next, the physicochemical analyzed SERWW was spiked with 30 mgL −1 of Pb(II) ions solution and reserved for the adsorption experiments. In order to assure reproducibility, all the experiments were conducted in triplicate, and the results were reported as average values.

Preparation of Cellulose and CNMs from Erythrina brucei.
e collected stem of the Erythrina brucei plant sample was confirmed by an Ethiopian botanist (Addis Ababa University, AAU; national herbarium). It was washed with distilled water repeatedly, dried with air at room temperature, and ground using a grinder carefully to form a coarse particle. For the extraction of CNMs, 9 g of the ground coarse particle and a 125 mL : 75 mL ratio mixture of toluene : ethanol solvent were added to a beaker and placed in a water bath for 46 hours at 50°C. Subsequently, the extracted mixture was washed with boiling water, filtrated, and dried in an oven at 50°C for 10 hours. en, the dried fibers were cut into short fibers of approximately 5 mm in length. Next, these short fibers were treated with 100 mL of 3.0 M NaOH solution at 50°C for 2.5 hours to remove the lignin and hemicelluloses present in lignocellulosic biomass. Afterward, this mixture was washed well with deionized water repeatedly until it becomes neutral. ereafter, the neutral mixture was centrifuged, filtered, and dried in an oven at 50°C for 10 hours. en, the dried mixture was ground into a pulp form and bleached with a 3 : 0.75 ratio mixture by volume of sodium chlorite (NaClO 2 ) to glacial acetic acid for 4 hours at 60°C under mechanical stirring. is procedure was repeated with half of the initial amount of bleaching agent. ereafter, it was centrifuged, washed repeatedly, and filtered, forming cellulose suspension. Subsequently, it was hydrolyzed by 100 mL of 6 M H 2 SO 4 for 2 hours to break up the cell wall and to separate the fibrils present for the production of cellulose nanomaterial (CNM) suspension through sonication. en, the prepared CNM suspension was centrifuged at 1600 rpm to separate the CNM from noncellulosic constituents and homogenized in homogenizer at 12,000 rpm for 2.0 hours. It was then washed, filtered, and dried in an oven at 50°C for 10 hours to form crystalline CNM. Finally, the prepared CNM was kept in a suitable place for characterization purposes. is procedure was adapted from Kara et al. [41] with modification, and the procedure was used throughout the experiments. e flow chart representation for the preparation of CNM is given in Figure 1.

Preparation of Chemically (Sodium Periodate) Modified CNM.
e vicinal hydroxyl groups at carbon atoms numbers 2 and 3 in an anhydroglucose unit of cellulose were oxidized to two aldehyde groups by simultaneously breaking the carbon-carbon bond between the carbon atoms numbers 2 and 3 by using sodium periodate reagent ( Figure 2). erefore, sodium periodate is known as a specific oxidant for cellulose-based materials. us, 0.2 gmL −1 of NaIO 4 was dissolved into approximately 2 wt% of CNM suspension in a 250 mL flask. e flask was carefully covered with aluminum foil and stirred at 50°C in the dark for 4 hours [42]. By the addition of 1 g ethylene glycol, the excess oxidizing agents were consumed, and the reaction was completed. is procedure produces dialdehyde cellulose nanomaterial (DACNM) through centrifugation at 1600 rpm for 40 min, and it was purified by successive water addition and centrifugation. is was sonicated for 3 min at 24 kHz (Branson Digital Sonifier S-450D, South Korea). Sodium periodate cellulose nanomaterial (NaIO 4 -CNM) was separated by centrifugation at 1600 rpm at 20°C, washed in deionized water several times until the pH of the washing medium was equal to pure water, and filtrated using filter paper no 42. Finally, the product was dried under vacuum at 50°C for 24 h. en, it was stored in a safe place for characterization purposes.

Characterization.
e crystallite size, functional groups, surface morphologies, and thermal stability of CNM and NaIO 4 -CNM sorbents were investigated by using XRD with Cu-Kα radiation (λ � 0.154 nm) at 40 kV and 30 mA in a diffraction angle of 2θ ranging from 10°to 80°at a scan rate of 3°/min, FT-IR, SEM, and TGA-DTG analysis, respectively.

Uptake Experiments.
For this experiment, the required amount of adsorbents such as CNM and NaIO 4 -CNM and 30 mL of Pb(II) ions solutions were mixed together in 100 mL flasks. e mixture was shaken thoroughly using an orbital shaker. Subsequently, for the absorbance measurement of Pb(II) ions solutions, atomic absorption spectrophotometer (AAS, Shimadzu, USA) was used. All the uptake experiments were performed by measuring various factors that were inducing the Pb(II) ions uptake ability such as solution pH, adsorbent dose, contact time, agitation speed, and initial Pb(II) ions concentration. e effect of each parameter on the Pb(II) ions uptake ability was examined by Journal of Chemistry keeping all other parameters at constant values. ese parameters were determined by ranging the initial concentration of Pb(II) ions from 5 to 50 mg/L, adsorbent dosage from 0.01 to 2.5 g, contact time from 30 to 180 min, solution pH from 1 to 9, and temperature from 25 to 40°C.

Point of Zero Charge (pHPZC).
e solution pH circumstance in which the surface charge density equals zero is termed as the pHPZC. To determine the pHPZC, the prepared adsorbents were added to 30 mL Pb(II) ions solutions with an initial pH of 2.0 to 9.0. e pH of the solution was adjusted using 0.1 M NaOH and 0.1 M HCl solutions. e suspensions were agitated on an orbital shaker at a shaking speed of 250 rpm at room temperature for 120 min. Finally, optimum pH was determined. e pHPZC was calculated using where pH 1 is the pH value before the experiment and pH 2 is the pH value after the experiment. In the plot of ∆pH vs pH, the intersection points at which ∆pH � 0 specify pHPZC.

Uptake Isotherms.
Mathematically, the affinity of the Pb(II) ions uptake for CNM and NaIO 4 -CNM adsorbent was measured using adsorption isotherms. us, the adsorption of Pb(II) ions by using CNM and NaIO 4 -CNM sorbents was done using (2) and (3). From these equations, one can understand that the amount of Pb(II) ions adsorbed onto the CNM and NaIO 4 -CNM adsorbents is equal to the amount of Pb(II) ions that were removed from the SERWW samples.
where q e and q t represent the amount of pollutant adsorbed onto adsorbent surfaces at equilibrium and any specified time (mgg −1 ), respectively.   SERWW sample (L). Initial and equilibrium concentrations were used to determine the percent Pb(II) ions removal and represented in e thermodynamic study of the uptake process was conducted by investigating the basic thermodynamic parameters such as a change in Gibbs free energy (∆G), change in enthalpy (∆H), and change in entropy (∆S) values [44,45]. erefore, in order to determine the thermal behavior of the uptake phenomenon, all predetermined and optimized values of parameters (solution pH, sorbent dosage, contact time, agitation speed, and Pb(II) ions initial concentration) were used, and the temperature was varied from 25 to 40°C.

Uptake Kinetics.
e rate of Pb(II) ions uptake process was accomplished by using the contact times ranging from 30 to 180 min by putting all parameters such as solution pH, sorbent dose, agitation speed, and Pb(II) ions initial concentration at constant values.

Regeneration Test.
From both adsorbents, NaIO 4 -CNM was selected for sorbent regeneration study due to the higher Pb(II) ions uptake abilities, and the study was performed in removing Pb(II) ions from SERWW through replicating the laboratory work using the same NaIO 4 -CNM sorbent for at least 13 successive cycles. Desorption of Pb(II) ions was carried out by mixing 1 g of NaIO 4 -CNM adsorbent previously used for removing purpose with 10 mL of 0.1 M HCl solution in a 100 mL flask. en, this mixture was stirred in an orbital shaker for 25 min. ereafter, the NaIO 4 -CNM sorbent was separated from the solution using centrifugation. e separated NaIO 4 -CNM sorbent was then washed with deionized water six times, dried in the oven at room temperature, and reapplied for at least 13 successive adsorption-desorption cycles.

Results and Discussion
3.1. Characterization. Different characterization techniques, such as TGA-DTG, FT-IR, XRD, and SEM were tested to determine thermal stability, functional groups, crystallinity, and surface morphology, respectively, of CNM and NaIO 4 -CNM sorbents. Specifically, the crystallinity of the sorbent materials was determined with the help of XRD spectrometry (Figure 3(a)). e XRD spectra indicated that the oxidized (NaIO 4 -CNM) sorbent has similar peaks to the pristine CNM peaks (Figure 3(a)), and they evidently presented an amorphous nature rather than 100% crystallinity because the adsorbent materials were prepared from polymeric materials. e representative peaks at 16.16°and 22.24°f or the oxidized nanocellulose (NaIO 4 -CNM) revealed a reduced degree of crystallinity compared to the pristine CNM, as the noncompact region of the crystalline part was oxidized progressively by the reaction of NaIO 4 chemicals with cellulose nanomaterial suspension. Certainly, the peaks at 2θ � 16.16°, 22.24°, 26.6°, and 34.41°are represented by (110), (110), (200), and (004) crystallographic planes of cellulose I, respectively [46,47]. From the XRD spectra, the crystallite particle sizes were calculated using Debye Scherrer equation (5) for both adsorbents, and the values were 2.28 nm and 2.70 nm for NaIO 4 -CNM and CNM, respectively.
where D s is mean crystallite size (nm), λ wavelength of the incident radiation (λ � 0.15405 nm), ß pure diffraction broadening (radians), and θ the Bragg angle (degrees, halfscattering angle). Usually, β is taken as the full width at half the maximum of the major diffraction band (FWHM). e identification of functional groups and surface characteristics of the prepared CNM and NaIO 4 -CNM sorbents was carried out by using FT-IR spectroscopy. eir spectrum was presented in Figure 3(b). e spectra have shown two major absorption zones in the ranges of 2925-3385 cm −1 and 611-1058 cm −1 . Based on these spectral zones, the CNM and NaIO 4 -CNM sorbents have several functional groups which display either stretching vibration or bending vibration. ese are (broadband around 3385 cm −1 ) detected for both sorbents, indicating the presence of O-H free stretching vibration of the CH 2 -OH structure on cellulose I [49]. e bands found in the region of 2855 cm −1 are because of the stretching vibration of C-H in cellulose I, and the bands situated at 1644 cm −1 are attributed to the O-H bending vibrations of cellulose I. e peaks detected at 1458 cm −1 match the C-C stretching and/ or CH 2 symmetric bending in aromatic groups of cellulose I. e peaks located at 1058 cm −1 are associated with stretching vibration of C � O groups [50]. Compared with the spectrum of pristine CNM, additional peaks were observed in oxidized cellulose nanomaterial (NaIO 4 -CNM) at 1730 cm −1 , referring to the stretching vibration of the carbonyl group (C � O) for aldehyde due to the formation of dialdehyde cellulose nanomaterial (DACNM). ese recommend that sodium periodate oxidizes the adjacent hydroxyl groups of cellulose at locations of carbon numbers 2 and 3 into aldehyde groups, simultaneously breaking the corresponding carbon-carbon bond of the glucopyranose ring in order to obtain DACNM. In addition, the increased intensity of NaIO 4 -CNM was observed compared to CNM due to the presence of aldehyde carbonyl functional groups on the surface of NaIO 4 -CNM. is result was in agreement with the study reported by Xiangyu et al. [51] on cationic dialdehyde nanocellulose from sugarcane bagasse for efficient chromium (VI) removal.
SEM characterization was carried out to obtain information about the surface morphology of both CNM and NaIO 4 -CNM adsorbents. e SEM images with cylindrical rod-like shapes for both CNM and NaIO 4 -CNM adsorbents are indicated in Figures 3(c) and 3(d). ese images show that NaIO 4 -CNM sorbent was likely to agglomerate in comparison with CNM adsorbent after drying. e addition of NaIO 4 to CNM suspension during the oxidation process initially degrades the amorphous regions of NaIO 4 -CNM,   Journal of Chemistry and the progressive oxidation reaction takes place into the crystalline regions. Finally, aldehyde groups gained from the oxidation reaction were added to the hydroxyl groups to yield hemiacetal. ese variations in biochemical arrangements also caused variations in surfaces of NaIO 4 -CNM [52]. As a result, the rode-like structure was well observed in NaIO 4 -CNM adsorbent after oxidation and indicated a larger specific surface area with a smaller average diameter than the pristine CNM [53]. e thermogravimetric analysis with differential thermogravimetry (TGA-DTG) behaviors of CNM and NaIO 4 -CNM adsorbents are presented in Figures 3(e) and 3(f), respectively. Analyses of samples revealed slight weight loss at low temperature (<100°C) conforming to the vaporization of absorbed water. e TGA revealed three phases of decomposition (Figure 3(f)). Initially, 10% of mass loss was observed in the temperature range of 40-83.03°C corresponding to the dehydration and decomposition of cellulose nanomaterials. Secondly, almost 48.853% of mass loss was observed in the temperature range of 252. .309°C corresponding to the scission of cellulose structure and chain, hence the discharge of CO and CO 2 and the production of carbonaceous residues [54,55]. irdly, a very slow mass loss of about 14.097% was revealed after 500°C, corresponding to the decomposition of residual substances, due to the oxidation of char. Moreover, the DTG curves showed that the maximum weight loss is 411.22°C and 397.17°C for CNM and NaIO 4 -CNM adsorbents, respectively (Figure 3(f)). In addition, the initiating temperature of degradation for NaIO 4 -CNM was slightly lower than that of CNM, which may be expected as the periodate oxidation breaks the highly ordered bonding of crystalline CNM [56]. In general, a slight shift of NaIO 4 -CNM curves for both TGA and DTG was possibly observed due to the presence of carbonyl functional groups on the backbone of NaIO 4 -CNM and increased the hydrophilicity, and this provides a lower thermal decomposition temperature [57].

Physicochemical Properties of the SERWW.
e experimentally measured values for the physicochemical properties of SERWW were indicated in Table 1. e pH values and electrical conductivity values were measured in different series, and the average values of 6.15 ± 0.03 and 260 ± 0.5, respectively, were reported (Table 1). From these results, it is possible to conclude that SERWW taken from near Modjo industries was nearly acidic. Besides, the chemical oxygen demand (COD), biological oxygen demand (BOD), total phosphorus (TP), total inorganic nitrogen (TIN), nitrate (

Effect of Initial Concentration.
e effect of initial Pb(II) ions concentrations (Ci) for the removal of Pb(II) ions from SERWW using CNM and NaIO 4 -CNM sorbent is given in Figure 4(a). At the starting point, the removal process was very fast, due to the presence of a large vacant surface area of the CNM and NaIO 4 -CNM sorbents. At increased initial concentrations (Ci), the removal ability gradually increased, moved toward the optimum value, and reached the optimum amount of 30 mg/L. At this amount, both CNM and NaIO 4 -CNM sorbents evidently displayed maximum Pb(II) ions uptake ability of 67.3% and 96.5%, respectively. Furthermore, a relatively higher uptake ability of Pb(II) ions was manifestly detected for NaIO 4 -CNM sorbent than that for CNM sorbent.
is is because the surface area of NaIO 4 -CNM adsorbent was relatively increased by the surface functionalization of CNM with NaIO 4 . Supporting this result, Chen et al. [58] reported research on As(III) removal by nanostructured dialdehyde cellulose−cysteine microscale and nanoscale fibers.

Effect of Contact Times.
e effect of contact time on the Pb(II) ions removal was examined by using experiments at an agitation speed of 250 rpm, optimum CNM and NaIO 4 -CNM dose of 1 g, temperature (T) of 25°C, and initial concentration of Pb(II) ions of 30 mg L −1 (Figure 4(b)). e %R of Pb(II) ions for both CNM and NaIO 4 -CNM rose with raising the time up to the optimum contact time of 120 min, due to the presence of highly active sites on the surfaces of the adsorbent [59]. e maximum %R values of 72.2% and 96.8% were observed for both CNM and NaIO 4 -CNM sorbents, respectively, at the optimum time of 120 min. After this time, the %R processes became at equilibrium and proceeded in a fixed manner. e maximum Pb(II) ions uptake abilities were detected for NaIO 4 -CNM sorbent compared to CNM mainly because of the increased active sites of the sorbent surfaces possessing a large number of reactive aldehyde carbonyl groups and carboxylate groups.

Effect of Adsorbent Dose.
Experiments for the %R of Pb(II) ions from the SERWW at different temperatures of 25, 30, and 40°C using CNM and NaIO 4 -CNM adsorbent were conducted and reported at the optimum temperature of 25°C ( Figure 5). During the experiment, the impact of the adsorbent dose was done by varying the amount of CNM and NaIO 4 -CNM sorbents from 0.04 to 2.5 g, at the optimum initial concentration of 30 mg L −1 , agitation speed of 250 rpm, solution pH of 6, and contact time of 120 minutes.

Figures 5(a) and 5(b) exhibited increased trends of Pb(II) ions %R for both CNM and NaIO 4 -CNM sorbents initially.
is trend is in agreement with research work reported by Alipour et al. [60] for Pb(II) ions removal using thioureafunctionalized magnetic ZnO/nanocellulose composite. e results also indicated that 97.8% of Pb(II) ions can be removed from wastewater by NaIO 4 -CNM sorbent with an optimum sorbent dosage of 1 g at 25°C. Dissimilarly, 72.5% of Pb(II) ions can be removed from wastewater by CNM sorbents with an optimum sorbent dosage of 1 g at 25°C. e increased %R of Pb(II) ions by NaIO 4 -CNM sorbent was due to the increased specific surface area resulting from the surface modification reactions.
is increased specific Journal of Chemistry surface area with smaller particle size resulted in a higher Pb(II) ions uptake ability since the oxidation ability of the hydroxyl groups was weaker than that of the aldehyde groups, and thus the uptake ability of CNM was lower than that of NaIO 4 -CNM [61]. On the whole, to summarize, for both adsorbents, the %R of Pb(II) ions increased by increasing the adsorbents dosage to optimum values, and after that value the removal ability decreases. is is anticipated     [63]. Furthermore, a much higher percentage of Pb(II) ions removal, 97.8%, was observed by using NaIO 4 -CNM adsorbent than that using CNM adsorbent. is is due to the increased specific surface area with very small particle size obtained as a result of CNM oxidation with NaIO 4 [64].

Effect of Solution pH.
e solution pH circumstance in which the surface charge density equals zero is termed as the pH point of zero charge (pHPZC). Figure 6(a) indicated the pHPZC of the material and its value was 5.0. From the plot, it is possible to deduce that the adsorbent surface is positively charged at pH < 5.0 and becomes negatively charged at pH > 5.0. us, for pH values < 5.0, the repulsive electrostatic force of attractions between the Pb(II) ions and positively charged functional groups of the CNM and NaIO 4 -CNM adsorbents was dominated, and the uptake process was decreased [65]. erefore, this recommended that higher %R of Pb(II) ions was observed at pH > 5 value, because, at solution pH > 5, the adsorbent surfaces are negative and thus react electrostatically with positively charged Pb(II) ions.
e effect of solution pH on %R of Pb(II) ions is indicated in Figure 6(b). CNM and NaIO 4 -CNM adsorbents show high removal abilities in the solution pH range of 5-9. is is because, when the pH solution exceeds the pHPZC of the adsorbent, the surface of the adsorbent is negatively charged creating favorable conditions for Pb(II) cation uptake. is result indicated that electrostatic attraction was the main mechanism controlling the uptake of the Pb(II) ions. At low pH values, the interaction of Pb(II) ions with sorbents is decreased because of the competition of H + ions and other matrices for the surfaces of CNM and NaIO 4 -CNM. In the other words, as the SERWW pH raises (i.e., less H + ions), the attachment of Pb(II) ions to the CNM and NaIO 4 -CNM adsorbents leads to the increased %R at the pH value of 6. Conversely, if the pH is greater than 6, then the level of OH− ions in the SERWW increases.
is phenomenon leads to the exchange of a few Pb(II) ions on the surfaces of CNM and NaIO 4 -CNM adsorbents. Accordingly, the optimum pH for Pb(II) ions removal by both CNM and NaIO 4 -CNM adsorbents was found to be 6. In line with this study, Olivera et al. [66] reported the maximum percent removal of Pb(II) at a pH value of 6. Supporting this view, we also made a similar report of our previous study [67]. Again, these results were in agreement with the study conducted by Qinghua et al. [68] on the uptake of Pb(II) from aqueous solutions using black wattle tannin-immobilized nanocellulose that showed increment with increasing the pH of solution form 2 to 6, and the highest adsorption capacity was observed at pH 6. At alkaline pH value, anions obtained from (HO − ) were more dominant, and the force of attraction for Pb was raised. Yeol et al. [69] showed that the increased %R of Pb(II) ions in the pH ranged from 2 to 7 using thiolfunctionalized cellulose nanofiber membranes. It was reported that for pH > 7 the Pb(II) ions precipitate as Pb(OH) 2 . Generally, results indicated that higher %R of Pb(II) ions was observed for NaIO 4 -CNM adsorbents than that for CNM sorbent at a pH value of 6 ( Figure 6(a)). is difference was due to the increased active sites in the surface structures of NaIO 4 -CNM adsorbent compared to CNM adsorbent.

Effect of Agitation Speed.
e effect of agitation speed on Pb(II) ions removal is shown in Figure 6(b). Initially, the agitation speed was slow, but as the agitation speed was increased subsequently, a rapid increase in the removal capability of Pb(II) ions was observed. is is because of the presence of fresh and smaller-sized adsorbent particles and more active sites on the binding surface of the adsorbent [70]. us, the removal ability of Pb(II) ions by NaIO 4 -CNM adsorbent was increased from 73.29 to 95.72% as the agitation speed was increased from 100 to 250 rpm. In the same way, the Pb(II) ions removal ability of the CNM adsorbent was increased from 40.5 to 70.4% as the agitation speed increased from 100 to 250 rpm ( Figure 6(b)). When the Pb(II) ions removal ability of the pristine CNM was compared with that of the functionalized cellulose nanomaterial (NaIO 4 -CNM), higher removal ability was observed for NaIO 4 -CNM due to the presence of more accessible surfaces resulting from the addition of the NaIO 4 to the CNM. For both adsorbents, the maximum Pb(II) ions removal capability was obtained at the optimum agitation speed of 250 rpm. is result was in agreement with the study reported by Mahmood et al. [71]. Generally, increasing the speed of agitation resulted in higher pollutant uptake abilities and helped to control the resistance of external mass transfer. Table 2 presents a summary of the experiments carried out to determine the effects of organic matter (OM) and nutrients (N and P) on the %R of Pb(II) ions. e experiments were carried out using water samples having variable levels of COD and NOM. e water sample used in the experiments includes synthetic wastewater (SW) with initial COD level ≈ 0 mg L −1 , SERWW with average COD level of 48.5 ± 0.5 mg L −1 , and SERWW mixed with natural organic matter (NOM) with an average COD Journal of Chemistry 9

e Chemistry of SERWW.
level of 104.0 ± 0.2 mg L −1 . Here, the SW was used as a control in the experiment because it is free of TIN, TP, and COD � 0 mg/L. e results indicated that increasing the OM level from COD ≈0 mg L −1 to 104.0 ± 0.2 mg L −1 displayed a decrease in the %R of 7.0%. A decrease in the %R of Pb(II) ions by increasing the OM level resulted from the interaction between the OM and Pb(II) ions. is interaction slightly inhibits the %R of Pb(II) ions by CNM and NaIO 4 -CNM adsorbents and decreases the %R capability of Pb(II) ions. Furthermore, the electrostatic force of attraction between the Pb(II) ions and the CNM and NaIO 4 -CNM adsorbents is the slow step. is suggested that the electrostatic force of  attraction between the OM and the active sites on the CNM and NaIO 4 -CNM adsorbents is restricted and does not influence the removal of Pb(II) ions from real wastewater. erefore, it revealed that the anticipated knowledge can still be practical for contaminant removal from wastewater.
Additionally, the effect of N and P on the %R of Pb(II) ions from wastewater was determined by using the previously used water samples. Results confirmed that the Pb(II) ions uptake abilities of CNM and NaIO 4 -CNM adsorbents were decreased by increasing the amount of nitrogen and also slightly affected by the increment of the amount of organic matter, but not affected by the increment of the amount of phosphorous and other constituents in the SERWW.

Adsorption Isotherms.
To understand the mechanism of Pb(II) ions uptake by CNM and NaIO 4 -CNM adsorbents, Langmuir (6), Freundlich (8), and Temkin (10) Table 3 illustrates the corresponding parameter values and the correlation coefficient (R 2 ) values, obtained from each plot. Higher R 2 values for both Langmuir and Freundlich isotherms have shown that the Langmuir and Freundlich isotherm models better fit the isothermal uptake data than the Temkin model. is suggested that the surfaces of CNM and NaIO 4 -CNM adsorbents were heterogeneous and physically compatible with monolayer adsorption and the adsorption process was favorable. Moreover, strong electrostatic interactions formed between the Pb(II) ions and the surfaces of adsorbents [72]. e favorability of the uptake process was due to n value that lies between 1 and 10, and the strong interactions between the adsorbates and surfaces of the adsorbents were because 1/n < 1.
e fundamental nature of the Langmuir model could be also determined by a dimensionless equilibrium parameter (RL), and its value was calculated using (7) [74]. e values (0.057 and 0.195) of RL < 1 suggested that the uptake process of Pb(II) ions by both CNM and NaIO4-CNM was a favorable process. Moreover, Table 3 has shown that the maximum uptake capacity of both CNM and NaIO 4 -CNM adsorbents was 91.74 and 384.62 mg/g, respectively.where Q max is the maximum uptake ability of Pb(II) ions per unit mass of adsorbent (mg g −1 ), K f is the uptake ability of the CNM and NaIO 4 -CNM sorbents (mgg −1 ), and n is the binding intensity. T is the absolute temperature in Kelvin, R is the ideal gas constant (8.314 J mol −1 K −1 ), and K C is the equilibrium constant calculated by multiplying the Pb(II) molar weight by the Langmuir constant (b).
log qe � log k f + 1 n log Ce, e spontaneity and feasibility of the Pb(II) ions uptake process were evaluated by investigating the basic thermodynamic parameters such as a change in Gibbs free energy (∆G), change in enthalpy (∆H), and change in entropy (∆S) values. Results have shown that the calculated ΔG (kJmol −1 ) value presented in Table 3 was negative and confirmed that the Pb(II) ions uptake mechanism was spontaneous and feasible.
Q t � k p t 0.5 + C i . (13) e kinetics data are presented in Table 4 with maximum correlation coefficient values (R 2 � 0.965 and 0.970, for PSO) and unsatisfactory correlation coefficient values (R 2 � 0.576, 0.837, 0.703, 0.542 for PFO and interparticle diffusion model) by CNM and NaIO 4 -CNM sorbents for Pb(II) ions uptake, respectively. us, R 2 values indicated that PFO and intraparticle diffusion kinetic models were too poor and not suitable for Pb(II) ions adsorption. erefore, Figures 8(a) and 8(b)) indicate representative fitness of the data for PSO for Pb(II) ions uptake by CNM and NaIO 4 -CNM sorbents and suggest that the uptake process is chemisorption. Moreover, to support this view, the application of Root Mean Square Error (RMSE) calculations for the statistical evaluation of data is very important. us, the RMSE values for CNM and NaIO4-CNM adsorbents were 0.493 and 0.013, respectively, given in Table 4. From these values, it is possible to conclude that the calculated value and experimental value were closer to each other and confirm a representative fitness of the data for PSO for Pb(II) ions uptake by CNM and NaIO 4 -CNM sorbents.

Adsorption Mechanism.
e probable mechanism of Pb(II) ions uptake by CNMs is schematically represented in Figure 9. From the figure, it could be inferred that the hydroxyl, carbonyl, and carboxyl groups are mainly responsible for the uptake of Pb(II) ions: Pb 2+ (aq) + R(OH,CO,COOH) ⟶ Pb(R(OH,CO,COOH)) 2+ .   is adsorption mechanism was performed via electrostatic interactions between the Pb(II) ions and the hydroxyl, carbonyl, and carboxyl groups, and chemical activity of these functional groups on the surface of CNMs contributes to the uptake process.   isotherm model. As can be observed in Table 5, the uptake capacity of both adsorbents in this study is higher than that of the majority of the adsorbents reported in the literature [81][82][83][84][85][86][87]. Furthermore, the uptake of Pb(II) ions by tanninnanocellulose (TNCC) at the same pH of 6 has lower uptake capacity than the present adsorbents Pb(II) ions uptake capacity. is approves the possibility of using CNM and NaIO 4 -CNM adsorbents with cost effectiveness, in comparison to other previously used adsorbents. Because of their simplicity, nontoxicity, cost effectiveness, and biodegradability, CNM and NaIO 4 -CNM adsorbents have great potential for effective removal of Pb(II) ions from real WW.

Regeneration Test.
Because of its exceptional uptake ability as sorbent material, NaIO 4 -CNM was carefully chosen for recycling experiments. e desorption and regeneration experimental procedures were done by evaluating the %R of Pb(II) ions after the 1st, 4th, and 13th cycles and presented in Figure 10. e purpose of regeneration experiments was to make a cost-friendly contaminant uptake process from wastewater. is was done by using desorption experiments. Desorption of Pb(II) ions from the sorbents was performed with the help of HCl solution. e regenerated sorbent was reused for at least 13 cycles, and it was shown that the uptake ability of Pb(II) ions for NaIO 4 -CNM sorbent progressively decreased with increasing the cycles of reusable trial. e decrease in uptake ability of the sorbent with increased frequency of reusability times is normal, because of the loss of active sites on the NaIO 4 -CNM sorbent [88]. However, it was found that the uptake ability of the NaIO 4 -CNM sorbent did not meaningfully change after the 13th cycle of the procedure as the %R was up to that point advanced. e results have shown that the %R for the 13 consecutive cycles was decreased below 5.5%. From this result, it is possible to conclude that NaIO 4 -CNM sorbent can be used for contaminant uptake for a long time with an exceptional possibility. e results were in Figure 9: Adsorption mechanism of Pb(II) ions removal by CNMs.  agreement with the review study conducted by Chang et al. and Chu et al. [89,90] on the removal of heavy metals from wastewater by using molybdenum disulfide sorbent.

Conclusion
Biodegradable and biocompatible pristine and chemically modified cellulose nanomaterials were prepared by sulfuric acid hydrolysis methods. e as-prepared adsorbent materials were employed as cost-effective, easily recyclable, and nontoxic materials, with high uptake abilities, for the uptake of Pb(II) ions from real wastewater. e proposed mechanisms for the uptake process under the optimum circumstance of NaIO 4 -CNM adsorbent mainly involve the interaction of ester, carboxyl, and hydroxyl groups of cellulose with Pb(II) ions that resulted in higher Pb(II) ions uptake ability for the functionalized adsorbent than the pristine one. e uptake mechanism fits with Langmuir and Freundlich uptake isotherm models, and the kinetics of Pb(II) ions uptake by CNM and NaIO 4 -CNM adsorbents were described with the help of the PSO kinetics model. Both CNM and NaIO 4 -CNM adsorbents showed the maximum adsorption capacity of 91.74 and 384.62 mgL −1 at an optimum pH value of 6. For the regeneration study, NaIO 4 -CNM adsorbent was selected because of its high uptake ability, and the results of regeneration experiment have proven that it was recyclable and economically friendly material reused for different successive cycles. From this point, one can conclude that NaIO 4 -CNM adsorbent proved to be a cost-effective and environmentally friendly adsorbent for the uptake of Pb(II) ions from wastewater.

Data Availability
e data used to support the results of this study are included within the article.

Conflicts of Interest
e authors declare no potential conflicts of interest with respect to the research, authorship, and/or publication of this manuscript.