Investigating the Potential of Greener-Porous Graphene for the Treatment of Organic Pollutants in Wastewater

: Pharmaceuticals have emerged as a new class of ecological pollutants and have majorly contributed to harmful effects on the environment and human health. The presence of these pharma-ceuticals in wastewater treatment plants, ground, and seawater has been reported widely. Organic dyes and other organic contaminants which are being considered as emerging contaminants are now in the race among the top organic pollutants that need effective treatment. Removal of these contaminants via green adsorbents has become an essential requirement towards a green and cleaner environment. Herein, we report the efﬁcacy of the novel greener porous graphene obtained via the near-green synthesis method as an adsorbent material for treating seven organic pollutants: Methyl orange, Methyl red, Rhodamine-B, Ciproﬂoxacin, Atenolol, Ibuprofen, and Carbamazepine. Batch tests were conducted to investigate the effect of adsorption time and varying adsorbent dosages. The obtained greener porous graphene showed fast kinetics, which was determined to be guided by pseudo second-order kinetics and the maximum pollutant removal efﬁciency (>80%) was seen at a high adsorbent dosage (2 mL injected from a 5 g/L solution). Furthermore, the nonlinear adsorption modeling conﬁrmed that the greener porous graphene followed the Langmuir model for the dye rhodamine-B sorption and the Freundlich model for all the other six contaminants. This greener porous graphene can be considered an effective adsorbent for the removal of organic pollutants in wastewater.


Introduction
Two major industries, i.e., medical and textile, have created a socio-economic milestone in human history [1,2].Textile industries dispose of their effluents at a rapid rate, and their residue in water sources has caused great concern for human as well as aquatic life [3].The WHO declared that 4000 children die almost every day due to waterborne diseases originating from inefficient water and wastewater treatment [4].
Of these industrial effluent pollutants, organic dyes are carcinogenic to human health and are prominent noxious contaminants for the environment [5].Organic dyes account for 15% of the world's total dye production, which is disposed of as waste from fabrics and textile industries [6].Organic dyes such as Methyl orange (MeO), Methyl red (MeR), and rhodamine-B (RD) are frequently used dyes in the fabric dyeing process.MeO is a watersoluble azo dye with considerable mutating properties.The presence of this dye inside the human body can cause serious diseases, such as intestinal cancer [7].Deterioration in kidneys, liver, lungs, or even nervous systems are all resultant effects of the presence of dyes in the body.MeR is an anionic azo dye that irritates the eye, skin, and gut when ingested [8].On the other hand, RD is a cationic azo dye that comes with harmful effects, such as dermatitis (skin irritation) and skin cancer [9].Therefore, these dyes must be treated effectively instead of being disposed of in water bodies.Pharmaceuticals have increased human quality of life and have helped us fight dangerous diseases.However, their frequent presence in water sources through several means is now a growing concern and they are viewed as 'emerging contaminants (ECs)' [10][11][12][13][14][15][16][17][18][19][20][21][22][23][24].Due to their considerable presence in the environment, they are often referred to as 'pseudo persistent' contaminants [11,[25][26][27][28]. Groundwater and surface water both contain some pharmaceutical remnants with concentrations nearly less than 100 ng/L, while treated water contains these contaminants at concentrations below 50 ng/L [29].These levels are soaring across the world, daily, and according to the authors of [30], a very high concentration of pharmaceuticals is present in African and European waters.
Pharmaceuticals commonly found in UK waters are Atenolol (AT), Ibuprofen (IBU), Ciprofloxacin (CPF), and Carbamazepine (CB) [31].AT is described as Beta-blockers (BB), commonly advised for hypertension, heart rhythmic disease, or myocardial infractions [32,33].CB is a frequent drug used in treatment lines for epilepsy and prevents human-embryonic cell growth [34,35].CPF is considered to be among the top ten fluoroquinolone antibiotics for treating bacteria and fighting infections [36,37], and the presence of this organic pollutant in the environment not only creates an ecological disbalance but also leaves long-term effects in the body when more than the prescribed dose is ingested [38].IBU is an anti-inflammatory drug, used for the treatment of pain, fever, and rheumatic disorders, and is very commonly used in the UK [39].If not removed efficiently from the wastewater, it has a detrimental effect on human health and the aquatic ecosystem [40].Therefore, there is an imperative need to treat the water and wastewater (containing these organic pollutants).
Removal of various contaminants through the adsorption process has proven to be the most efficient and cost-effective method [3,40].Adsorbents of hydrophobic nature have emerged as an effective removal means for both organic and inorganic contaminants [40].Porous graphene (PG), i.e., a carbon-based material with super-hydrophobicity, has surfaced as an effective adsorbent for the removal of contaminants such as dyes and heavy metals [3].PG has also been tested against six emerging contaminants, namely atenolol, carbamazepine, ciprofloxacin, diclofenac, gemfibrozil, and ibuprofen, at their trace concentrations and has been shown to have an effective removal efficiency (>99%) at low PG dosages (100 mg/L) [31].It also showed good recyclability and effective regeneration for up to four cycles [31].The removal efficiency of these pharmaceuticals was further increased using PG as a filter media in the adsorption column filter tertiary unit [41].Various composites, such as GNP/BNA (graphene nanoplatelet/Boron Nitride), with a maximum adsorption capacity of 185 mg/g, have proven to be potential candidates for the removal of ciprofloxacin [42].
Synthesis of PG via various methods has also been studied.Graphene oxide (GO) has proven to be the vital precursor to synthesize PG, and the most common chemical technique to obtain GO is the Hummers method [43].Several green techniques have been incorporated to achieve PG via GO as the common precursor [44][45][46].However, all these green methods use GO as a precursor, synthesized from the techniques involving noxious reactants resulting in the release of toxic gases into the environment.Thus, there is an absolute need for greener adsorbent materials.
A recent novel technique was demonstrated, where a greener method was obtained to synthesize a greener PG [47].The authors [47] reported a high yield of greener GO synthesized by oxidation of graphite via this near-green technique.The successful synthesis of the as-produced bi-layered greener PG was confirmed via various characterization techniques, such as Atomic Force Microscopy, Transmission Electron Microscopy, X-ray diffraction, and Scanning Electron Microscopy.Herein, for the very first time, we report the Brunauer-Emmett-Teller (BET) Specific Surface area of this novel greener PG and investigate its efficacy in removal the of seven emerging contaminants (ECs), such as AT, CB, CPF, IBU, MeO, MeR, and RD.
The aim of this study is to understand the potency of this novel greener PG, synthesized via a near-green route [47], for treating emerging contaminants in wastewater.For the very first time, this study outlined the removal efficacy of greener PG in water treatment applications and proved its potential as a candidate for an adsorbent material.BET measurements for this novel greener adsorbent were also carried out to investigate and compare the surface area of the PG derived commercially from noxious reagents.This research aimed to establish an environmentally friendly PG adsorbent in the field of wastewater/water treatment.
Preparation of greener PG-The material was obtained via near-green synthesis, as reported in ref. [47].
Preparation of commercial PG-Reduced graphene oxide (rGO) was placed overnight at 200 • C in a vacuum oven to obtain commercial PG.
Pharmaceuticals (AT, CPF, CB, and IBU) and organic dyes (MeO, MeR, RD)-Stock solutions were obtained by mixing pharmaceuticals and dyes with the de-ionized water (DW).To avoid the photo-degradation of these prepared stock solutions, airtight containers were used for their storage and were kept in a dark place.

Microstructural Surface Area Characterization
Brunauer-Emmett-Teller (BET) specific surface area (SSA), porosity, pore volume, and pore size of the greener PG were analyzed using a Quantachrome Autosorb-iQ gas area characterization analyzer.After being heated at 200 • C for four hours to flush out impurities lodged in the pores, the sample (greener PG) was cooled in an external bath at −195.8 • C.After that, the nitrogen gas (N 2 ) was applied, and the total volume and pressure were then measured.

Batch Tests and Analysis
All seven pollutants were tested in batches under various experimental settings, including contact time and varying greener PG doses.Each test was run three times, and the average result was used to analyze the data.

Effect of the Contact Time and Study of Kinetic Models
Without adjusting the pH of the contaminated solutions, kinetic experiments were conducted for the pollutants with a starting concentration of 10.0 mg/L (stock solution) throughout various time intervals, at room temperature (22 ± 3 • C) (AT, CB, CPF, IBU, MeO, MeR, and RD).Each of these 20 mL contaminant solutions was placed into 50 mL airtight sealed bottles.These contaminant solutions were then given a specific amount of adsorbent (1 mL injected from a suspension of 5 g of greener PG/L).The solutions were then each magnetically stirred for the allotted amounts of time (t = 5, 10, 15, 20, 40, 80, and 120 min).Finally, a 0.2 µm membrane filter was used to instantly filter the samples that were collected at the designated time.Two kinetic models: pseudo first-order (Equation ( 1)) and pseudo second-order (Equation (2)) were used to examine the reaction kinetics of the seven tested contaminants removal by greener PG [48]: where Q e (mg/g) refers to the equilibrium adsorption capacity, Q t (mg/g) is the adsorption capacity at a specific time 't', and k 1 (1/min) and k 2 (g/mg min) define the pseudo firstand second-order reaction rate constants, respectively.

Effect of the Adsorbent Dosage and Study of Adsorption Isotherms
The effects of injecting different adsorbent dosages such as 0.5, 1, 1.5, 2, 2.5, and 3 mL from a 5 g/L suspension into a specific contaminant concentration (10 mg/L) were investigated in this batch testing.The contaminants with varying adsorbent dosages were placed in a shaker for 24 h, and finally, the supernatants of the samples were collected using a 0.2 µm membrane filter.
Three models-Langmuir, Freundlich, and Temkin-were analyzed to evaluate the modeling of these seven contaminants' sorption onto greener PG [48]: where Q max (mg/g) refers to the maximum adsorption capacity determined by Langmuir, k L (L/mg) is the Langmuir isotherm constant, k F ((mg/g)(mg/L)1/n) is the Freundlich isotherm constant, and n (dimensionless and n = 1) is the constant governing heterogeneity and adsorption intensity.The universal gas constant is R (8.314 J/mol.Kelvin), the Temkin isotherm binding constant is k t (L/g), the Temkin isotherm constant is B t (J/mol), and the absolute reaction temperature is T (temperature in K).To further comprehend the adsorption process, the Langmuir separation factor (R L ) was also determined using Equation (6).The R L expresses (dimensionless) the favorability of the Langmuir modelbased adsorption process.R L = 0 denotes the irreversible adsorption, whereas R L = 1 promotes the linear adsorption.For there to be favorable adsorption, 0 < R L < 1.
For the best fit of the experimental data with the aforementioned models, in addition to a linear fitting, a nonlinear regression was also investigated.Additionally, this regression was taken into account to prevent mistakes from the nonlinear/linear transformation [49].Based on the lowest Akaike Information Criterion (AIC) value calculated, using Equation (7), this criterion for nonlinear regression is the most precise and trustworthy statistical comparison measure to compare the best-fitting models with the experimental data [50]: C 2023, 9, 97 where N refers to the number of experimental points, K denotes the total number of model parameters, and SSE stands for the Sum of Squared Errors, which is calculated as:

Morphological Study of the Greener PG
Morphological characterizations illustrated in ref. [47] confirmed the successful synthesis of greener PG obtained via a near-green technique.Herein, the BET SSA of this greener PG was obtained to understand the importance of greener PG's SSA in the adsorption of contaminants.Figure 1 depicts the isotherms and Barret Joyner Halenda pore size distributions of greener PG.As per the given IUPAC classification, the N 2 adsorptiondesorption isotherms curves for the greener PG sample demonstrated type IV with an H3 hysteresis loop revealing the same characteristics feature for mesopores [51,52].The adsorption segment of the nitrogen isotherms at P/P 0 showed a fast increase, implying the formation of large mesopores and macropores [51,53], with pore width calculated as 3-5 nm.The rest of the parameters of the greener PG sample obtained from the N 2 adsorption-desorption isotherms are shown in Table S2.The BET SSA of the greener PG was calculated as circa 289.146 m 2 g −1 , which is significantly higher than that of the previously reported commercial rGO-derived PG (circa 82.76 m 2 g −1 ) [3,54,55].This proved that the sample showed a porous morphology with a bi-layer structure, which in turn resulted in a large number of active adsorption sites for the electrostatic reaction and finally boosted the adsorption mechanism.
C 2023, 9, x FOR PEER REVIEW 5 of 23

Morphological Study of the Greener PG
Morphological characterizations illustrated in ref. [47] confirmed the successful synthesis of greener PG obtained via a near-green technique.Herein, the BET SSA of this greener PG was obtained to understand the importance of greener PG's SSA in the adsorption of contaminants.Figure 1 depicts the isotherms and Barret Joyner Halenda pore size distributions of greener PG.As per the given IUPAC classification, the N2 adsorptiondesorption isotherms curves for the greener PG sample demonstrated type IV with an H3 hysteresis loop revealing the same characteristics feature for mesopores [51,52].The adsorption segment of the nitrogen isotherms at P/P0 showed a fast increase, implying the formation of large mesopores and macropores [51,53], with pore width calculated as 3-5 nm.The rest of the parameters of the greener PG sample obtained from the N2 adsorptiondesorption isotherms are shown in Table S2.The BET SSA of the greener PG was calculated as circa 289.146 m 2 g −1 , which is significantly higher than that of the previously reported commercial rGO-derived PG (circa 82.76 m 2 g −1 ) [3,54,55].This proved that the sample showed a porous morphology with a bi-layer structure, which in turn resulted in a large number of active adsorption sites for the electrostatic reaction and finally boosted the adsorption mechanism.

Effect of Contact Time on the Contaminants' Removal
The effect of contact time on the adsorption of AT, CB, CPF, IBU, MeO, MeR, and RD onto greener PG for different time intervals, i.e., 5-120 min, are shown in Figure 2. A fast sorption rate (>90%) was seen during the first 40-50 min.Thus, for batch study, 120 min was the adequate period for the adsorption of these ECs onto greener PG.In total, 1 mL of greener PG dosage was used for all seven ECs to study the effect of contact time on the sorption performance of greener PG. Figure 2 shows concentration profiles at different contact time 't' (Ct) for ECs: AT, CB, CPF, and IBU.Fast sorption kinetics for the initial period of 60 min (indicating maximum adsorption) was observed for these four ECs, and then the adsorption rate declined with increasing time, prior to saturating after 60-80 min.Similarly, Figure 2, for dyes, MeO, MeR, and RD depict faster sorption kinetics for the initial period of 40 min and then the adsorption rate plummets with an increase in the contact time period.The results indicated an excellent adsorption performance of greener

Effect of Contact Time on the Contaminants' Removal
The effect of contact time on the adsorption of AT, CB, CPF, IBU, MeO, MeR, and RD onto greener PG for different time intervals, i.e., 5-120 min, are shown in Figure 2. A fast sorption rate (>90%) was seen during the first 40-50 min.Thus, for batch study, 120 min was the adequate period for the adsorption of these ECs onto greener PG.In total, 1 mL of greener PG dosage was used for all seven ECs to study the effect of contact time on the sorption performance of greener PG. Figure 2 shows concentration profiles at different contact time 't' (C t ) for ECs: AT, CB, CPF, and IBU.Fast sorption kinetics for the initial period of 60 min (indicating maximum adsorption) was observed for these four ECs, and then the adsorption rate declined with increasing time, prior to saturating after C 2023, 9, 97 6 of 19 60-80 min.Similarly, Figure 2, for dyes, MeO, MeR, and RD depict faster sorption kinetics for the initial period of 40 min and then the adsorption rate plummets with an increase in the contact time period.The results indicated an excellent adsorption performance of greener PG for these ECs, which was attributed to the availability of surface pores on the greener PG, reflected by its BET SSA in Figure 1.To further illustrate the sorption kinetics, two models (Equations ( 1) and ( 2)), i.e., pseudo first-order (Supplementary-S1) and pseudo second-order (Figure 3), were studied to understand the reaction kinetics of the seven ECs removal by the greener PG [48].Of these models, the pseudo secondorder rate model fitted the best for outlining the kinetic sorption of the seven tested ECs onto greener PG, as shown by the highest correlation coefficient values (R 2 = 0.99).Moreover, the Q e (adsorption capacity at equilibrium) values calculated for all seven pollutants, for the pseudo second-order model, were in close proximity to the Q e values obtained via the experiment.This indicates a linear relationship between t/Q t and time (where Q t is adsorption capacity at time 't'), reflecting the dependence of adsorption rate on adsorption capacity instead of adsorbate concentration.All the kinetic parameters for both models, along with their R 2 values, are listed in Table 1.Sorption kinetics can also be interpreted in terms of hydrophilicity and hydrophobicity of the adsorbents and contaminants, indicated by the n-octanol/water partition coefficient (log K ow values) [56].With the help of this indicator, it has previously been proven that IBU is hydrophobic [31], while CB [31] and MeR [57] both have a hydrophobic/phallic nature, which facilitates the adsorption kinetics with greener PG (having a super-hydrophobic nature).Similarly, the dyes, MeO and RD are also proven to have a hydrophobic nature [58,59], reflecting their rapid adsorption kinetics.These hydrophobic interactions between hydrophobes and water cause the hydrophobes (greener PG and ECs of hydrophobic nature) to attract each other and orient away from water [31,60], thus increasing the adsorption performance of greener PG for these hydrophobic contaminants.On the contrary, the hydrophilic nature of CPF and AT [31] reflects the slightly low adsorption onto greener PG.

Effect of Various Adsorbent Dosages on Contaminant Removal
To understand the removal potency of this greener PG, a batch adsorption test was conducted on these seven ECs for six different dosages of greener PG (0.5 mL, 1 mL, 1.5 mL, 2 mL, 2.5 mL, and 3 mL of adsorbent injected from a 5-g/L suspension).The results are shown in Figure 4.The experiment was run for 24 h to ensure that each of the contaminants reached its equilibrium.For all the contaminants, the experimental conditions were the same and are listed below in Figure 4.The figure shows that with the increase in adsorbent dosage, the removal efficiency for these seven tested ECs increased.Greener PG showed a greater removal efficiency (between 85-95%) for dyes (MeO, MeR, and RD) than for ECs (AT, CPF, CB, and IBU).Among the dyes, MeO and RD showed the highest removal efficiency (>90%) by greener PG, resulting from hydrophobe-hydrophobe attraction between greener PG and these two dyes.The greener PG showed an effective removal potency for the four ECs, i.e., AT, CPF, CB, and IBU, with a removal efficiency between 70 and 90%, and IBU showing the highest removal efficiency (94.4%), which is attributed to its hydrophobic nature.Table S1 summarizes the full data of the removal efficiency of the adsorbent for these seven ECs with varying greener PG dosages.These seven emerging contaminants were also tested against the commercially obtained PG and are illustrated in

Effect of Various Adsorbent Dosages on Contaminant Removal
To understand the removal potency of this greener PG, a batch adsorption test was conducted on these seven ECs for six different dosages of greener PG (0.5 mL, 1 mL, 1.5 mL, 2 mL, 2.5 mL, and 3 mL of adsorbent injected from a 5-g/L suspension).The results are shown in Figure 4.The experiment was run for 24 h to ensure that each of the contaminants reached its equilibrium.For all the contaminants, the experimental conditions were the same and are listed below in Figure 4.The figure shows that with the increase in adsorbent dosage, the removal efficiency for these seven tested ECs increased.Greener PG showed a greater removal efficiency (between 85-95%) for dyes (MeO, MeR, and RD) than for ECs (AT, C 2023, 9, 97 9 of 19 CPF, CB, and IBU).Among the dyes, MeO and RD showed the highest removal efficiency (>90%) by greener PG, resulting from hydrophobe-hydrophobe attraction between greener PG and these two dyes.The greener PG showed an effective removal potency for the four ECs, i.e., AT, CPF, CB, and IBU, with a removal efficiency between 70 and 90%, and IBU showing the highest removal efficiency (94.4%), which is attributed to its hydrophobic nature.Table S1 summarizes the full data of the removal efficiency of the adsorbent for these seven ECs with varying greener PG dosages.These seven emerging contaminants were also tested against the commercially obtained PG and are illustrated in Figure 5.Commercial PG showed less adsorption for each of these ECs as compared to greener PG.This could be attributed to the low specific surface area of the commercial PG mentioned in Section 3.1.Greener PG exhibited large meso-and macro-pores, which increased the overall surface area of this greener adsorbent and further acted as an adsorption site for the seven ECs.
greener PG.This could be attributed to the low specific surface area of the commercial PG mentioned in Section 3.1.Greener PG exhibited large meso-and macro-pores, which increased the overall surface area of this greener adsorbent and further acted as an adsorption site for the seven ECs.
After reaching the equilibrium, the concentration (Ceq) of each of these ECs was obtained at varying greener PG dosages.The concentration profiles for each of the seven tested ECs with various adsorbent doses are shown in Figure 6.All these seven contaminants displayed similar profiles, i.e., the concentration (Ceq) of each of these ECs decreased with the increasing doses of greener PG, indicating maximum EC adsorption at the highest greener PG dosage.This increase in adsorption with an increase in adsorbent dosages was aided by the adsorption capacity (Qe) curves for each EC shown in Figure 7. Contaminants IBU, MeO, and RD exhibit similar adsorption profiles, indicating their highest removal with maximum adsorption capacities: 37.86 mgg −1 (Figure 7d), 38 mgg −1 (Figure 7e), and 39.5 mgg −1 (Figure 7g), respectively.A very minimal variation in adsorption capacity was observed after 2 mL of greener PG dosage, contributing to nearly identical removal efficiencies of the contaminants for other two higher greener PG dosages.This proves that this greener PG obtained from near-green synthesis showed a considerable potential for water treatment application.After reaching the equilibrium, the concentration (C eq ) of each of these ECs was obtained at varying greener PG dosages.The concentration profiles for each of the seven tested ECs with various adsorbent doses are shown in Figure 6.All these seven contaminants displayed similar profiles, i.e., the concentration (C eq ) of each of these ECs decreased with the increasing doses of greener PG, indicating maximum EC adsorption at the highest greener PG dosage.This increase in adsorption with an increase in adsorbent dosages was aided by the adsorption capacity (Q e ) curves for each EC shown in Figure 7. Contaminants IBU, MeO, and RD exhibit similar adsorption profiles, indicating their highest removal with maximum adsorption capacities: 37.86 mgg −1 (Figure 7d), 38 mgg −1 (Figure 7e), and 39.5 mgg −1 (Figure 7g), respectively.A very minimal variation in adsorption capacity was observed after 2 mL of greener PG dosage, contributing to nearly identical removal efficiencies of the contaminants for other two higher greener PG dosages.This proves that this greener PG obtained from near-green synthesis showed a considerable potential for water treatment application.To study the adsorption behavior of greener PG, adsorption isotherms for each of these seven ECs were investigated [61].In this study, we examined three models-Langmuir (Equation (3)), Freundlich (Equation ( 4)), and Temkin (Equation ( 5)), in both their linear and nonlinear forms [48][49][50].In the case of linear modeling, the best-fitted adsorption model was expressed with the help of linear correlation coefficient R 2 and other intrinsic parameters, which are listed in Table S3.The Temkin model for all seven contaminants was eliminated, as the intrinsic parameter, B t , showed negative values [54,62,63].For all the seven tested contaminants, the R 2 values for these three models are highlighted in Table S3.
According to the values obtained for R 2 (>0.9),Freundlich and Langmuir showed the best fit for CPF, MeO, and RD contaminants, and the Freundlich model fitted the best for the contaminants AT, CB, IBU, and MeR, confirming multilayer adsorption of these contaminants onto greener PG.However, based on the other intrinsic parameters shown in Table S3, RD followed the Langmuir model as it showed a negative slope in the case of the Freundlich isotherm model, confirming the monolayer adsorption of the dye RD onto the greener PG [61].To study the adsorption behavior of greener PG, adsorption isotherms for each of these seven ECs were investigated [61].In this study, we examined three models-Langmuir (Equation (3)), Freundlich (Equation ( 4)), and Temkin (Equation ( 5)), in both their linear and nonlinear forms [48][49][50].In the case of linear modeling, the best-fitted adsorption model was expressed with the help of linear correlation coefficient R 2 and other intrinsic parameters, which are listed in Table S3.The Temkin model for all seven contaminants was eliminated, as the intrinsic parameter, Bt, showed negative values [54,62,63].For all the seven tested contaminants, the R 2 values for these three models are highlighted in Table S3.
According to the values obtained for R 2 (>0.9),Freundlich and Langmuir showed the best fit for CPF, MeO, and RD contaminants, and the Freundlich model fitted the best for the contaminants AT, CB, IBU, and MeR, confirming multilayer adsorption of these contaminants onto greener PG.However, based on the other intrinsic parameters shown in Table S3, RD followed the Langmuir model as it showed a negative slope in the case of the Freundlich isotherm model, confirming the monolayer adsorption of the dye RD onto the greener PG [61].
The nonlinear modeling was also studied for these three models [49,50].Freundlich's model showed the best fit for all the contaminants, except RD.For the six contaminants The nonlinear modeling was also studied for these three models [49,50].Freundlich's model showed the best fit for all the contaminants, except RD.For the six contaminants AT, CPF, CB, IBU, MeO, and MeR, a positive value of slope and the lowest AIC values (obtained from Equations ( 7) and ( 8)) were obtained for the Freundlich model, indicating the possibility of the involvement of physisorption in the adsorption process and heterogeneity in the greener PG surface.Separation factor values, R L , were also obtained for these six contaminants and showed either more than 1 or less than zero values, further indicating the Freundlich model being the best suited for these six ECs.RD showed the lowest AIC value for the Langmuir model, indicating the monomolecular adsorption on greener PG surface without any dye stacking.This was further confirmed with separation factor (R L = 0.94), obtained between 0 and 1, and contributing to the favorable adsorption process.This showed the possibility of a binary [63] sorption mechanism.The AIC values (highlighted as being the best-suited model) and other nonlinear intrinsic parameters were calculated for all seven contaminants (Table 2).

Figure 1 .
Figure 1.Measurement of the specific surface area.The pore size distribution of greener PG was calculated using the Barrett-Joyner-Halenda method as an inset at 77 K, with a pore size of 1-4 nm.

Figure 1 .
Figure 1.Measurement of the specific surface area.The pore size distribution of greener PG was calculated using the Barrett-Joyner-Halenda method as an inset at 77 K, with a pore size of 1-4 nm.

Figure 5 .
Figure 5. Equilibrium study for the seven tested emerging contaminants depicting their removal efficiency with varying (a) commercial PG Dosages and (b) greener PG Dosages.

Figure 5 .Figure 5 .
Figure 5. Equilibrium study for the seven tested emerging contaminants depicting their removal efficiency with varying (a) commercial PG Dosages and (b) greener PG Dosages.

Table 1 .
Kinetic parameters obtained for the two models, for emerging contaminants adsorption onto greener PG.R 2 is defined as the accuracy of the fitted model.

Table 1 .
Kinetic parameters obtained for the two models, for emerging contaminants adsorption onto greener PG.R 2 is defined as the accuracy of the fitted model.

Table 3 .
Comparison table of the adsorbents depicted in ascending order of their BET SSA, for water treatment application.