Methylene Blue Removal by Copper Oxide Nanoparticles Obtained from Green Synthesis of Melia azedarach : Kinetic and Isotherm Studies

: In this study, Melia azedarach fruit extract was used as a reducing agent and copper chloride dihydrate (CuCl 2 · 2H 2 O) was used as a precursor in the synthesis of copper oxide nanoparticles (CuO NPs). The UV–visible spectrum showed a characteristic absorption peak of CuO NPs at 350 nm. The surface properties of the adsorbent were analyzed through various techniques, indicating the successful formation of CuO NPs. The impacts of several factors, including initial pH (4 to 8), a dose of CuO NPs adsorbent (0.01–0.05 g), dye initial concentration (10–50 mg · L − 1 ), and contact times ranging from 5 to 120 min, were examined in batch adsorption studies. Based on the experimental results, the Langmuir isotherm is well-fitted, indicating MB dye monolayer capping on the CuO NPs surface with 26.738 mg · g − 1 as a maximum adsorption capacity Q m value. For the pseudo-second-order kinetic model, the experimental and calculated adsorption capacity values ( q e ) exhibited good agreement


Introduction
A cationic dye belonging to the thiazine dye family, methylene blue (MB), finds widespread applications in the textile, paper, and leather industries, as well as biological dyes [1].However, the discharge of MB and its derivatives into the environment has led to significant pollution issues.Consumption of MB dye by humans or animals may result in eye burns, fast breathing, vomiting, and nausea.Therefore, it is crucial to remove it from wastewater [2].Several effective wastewater treatment techniques for dye removal, such as flocculation or coagulation [3], adsorption membranes [4], biological treatment [5], electrochemical processes [6], and photodegradation [7], have been effectively adopted.
Recently, there has been a lot of interest in multifunctional materials due to the advancement of civilization and the growing need for smart materials.These materials were used to eliminate hazardous substances in the natural environment [8,9].Nanoadsorbents are a highly effective technology for eliminating organic dyes from water and wastewater.Their smaller size and increased adsorptive surface area make them particularly effective in this regard [10].Nanofibers, graphene, metal oxides, and carbon nanotubes are all examples of nano-adsorbents that can be used to improve the treatment of water and wastewater [11].
Copper oxide nanoparticles (CuO NPs) are a type of metal oxide nanoparticles that have potential applications in both science and industry [12][13][14][15].Various techniques for synthesizing CuO NPs include sonochemical methods [16], chemical precipitation [17], laser ablation in liquid [18], hydrothermal [19], sol-gel [20], and more.The chemical synthesis methods mentioned above are highly effective but have several limitations, such as high costs, utilization of hazardous chemicals and solvents, production of toxic waste, and high energy requirements.As a result, biosynthesis and other economical, environmentally friendly, biocompatible, and reliable approaches for producing nanoparticles have been developed.high energy requirements.As a result, biosynthesis and other economical, environmentally friendly, biocompatible, and reliable approaches for producing nanoparticles have been developed.
Melia azedarach, also known as chinaberry, is a tree species belonging to the Meliaceae family.It is native to Southeast Asia and Northern Australia and has been introduced to the Kurdistan region of Iraq.This tree is excellent for urban greening as it can absorb harmful and toxic gases and is also resistant to dust and smoke [33].Extracts from the leaves, fruits, and seeds of Melia azedarach have shown medicinal and pesticide properties against various pathogens and pests, respectively [34][35][36].
In the current research, for the first time, CuO NPs were synthesized using an aqueous extract from the Melia azedarach fruit.The effectiveness of the production process was demonstrated by investigating the adsorbent surface using various techniques.By calculating and analyzing equilibrium, kinetic, and isotherm parameters, the adsorption process was thoroughly explained.The results indicate that the environmentally friendly manufacture of CuO nanoparticles as an adsorbent shows great promise for successfully removing MB dye from aqueous solutions.This study is valuable for the protection and management of drinking water.Scheme 1 provides a schematic representation of the current work.
Scheme 1. CuO NPs adsorbent synthesis for MB dye removal.

Chemicals and Materials
Dried Melia azedarach fruits were collected from the University of Duhok College of Science gardens in Kurdistan, Region of Iraq.Copper chloride dihydrate (CuCl2•2H2O) was purchased from UNI-CHEM (Maharashtra, India).Methylene blue MB dye (chemical formula C16H18N3SCl•3H2O, λmax = 660 nm and molecular weight = 319.85g•mol −1 ), hydrochloric acid (HCl), and sodium hydroxide (NaOH), of 99% purity, were purchased from the German Sigma-Aldrich Company (Steinheim, Germany).The extract from the Scheme 1. CuO NPs adsorbent synthesis for MB dye removal., hydrochloric acid (HCl), and sodium hydroxide (NaOH), of 99% purity, were purchased from the German Sigma-Aldrich Company (Steinheim, Germany).The extract from the Melia azedarach fruits and the metal salt solution were prepared using distilled water (D.W).

Preparation of Melia azedarach Fruit Extract
Dried fruit of Melia azedarach were collected, carefully washed with D.W., and then left dry in the laboratory at 27 • C for 24 h to remove the remaining moisture.Following the grinding, 200 milliliters of D.W. were mixed with ten grams of ground powder in the beaker.The mixture was stirred at 150 rpm and heated to 70 • C for two hours.After allowing the extract to cool, it was filtered through filter paper Whatman No.1, yielding a pale-yellow extract that was subsequently refrigerated.This extract was reserved for future use in the production of the nanoparticles [37].

Synthesis of Adsorbent CuO NPs
The copper chloride dihydrate, CuCl 2 •2H 2 O, and Melia azedarach fruit extract were used to create the nanoparticles.With constant stirring and heating at 60 • C, 50 mL of (0.1 M) CuCl 2 •2H 2 O solution was gradually added to (75 mL) of Melia azedarach fruit extract in the beaker.The formed CuO NPs were detected in the solution through UV-vis spectra (Figure 1) by changing in color from blue to viscous green.After 24 h of incubation, the sticky precipitate was subjected to centrifugation for 10 min at 10,000 rpm, followed by three to four rinses with deionized water.Upon drying the precipitate at room temperature for 48 h, a pellet was formed.The ultimate product underwent a 2 h calcination process at 400 • C in a muffle furnace after being dried to eliminate plant-derived organic substances.Then, it was powdered and preserved for further usage [12].
Melia azedarach fruits and the metal salt solution were prepared using distilled water (D.W).

Preparation of Melia azedarach Fruit Extract
Dried fruit of Melia azedarach were collected, carefully washed with D.W., and then left dry in the laboratory at 27 °C for 24 h to remove the remaining moisture.Following the grinding, 200 milliliters of D.W. were mixed with ten grams of ground powder in the beaker.The mixture was stirred at 150 rpm and heated to 70 °C for two hours.After allowing the extract to cool, it was filtered through filter paper Whatman No.1, yielding a pale-yellow extract that was subsequently refrigerated.This extract was reserved for future use in the production of the nanoparticles [37].

Synthesis of Adsorbent CuO NPs
The copper chloride dihydrate, CuCl2•2H2O, and Melia azedarach fruit extract were used to create the nanoparticles.With constant stirring and heating at 60 °C, 50 mL of (0.1 M) CuCl2•2H2O solution was gradually added to (75 mL) of Melia azedarach fruit extract in the beaker.The formed CuO NPs were detected in the solution through UV-vis spectra (Figure 1) by changing in color from blue to viscous green.After 24 h of incubation, the sticky precipitate was subjected to centrifugation for 10 min at 10,000 rpm, followed by three to four rinses with deionized water.Upon drying the precipitate at room temperature for 48 h, a pellet was formed.The ultimate product underwent a 2 h calcination process at 400 °C in a muffle furnace after being dried to eliminate plant-derived organic substances.Then, it was powdered and preserved for further usage [12].

Characterization of CuO NPs
A spectrophotometer (Shimadzu UV-vis V-530A with a wavelength of 200 to 800 nm) was employed to determine the UV-vis absorption spectra of various substances.The synthesized CuO NPs were characterized using several techniques: field emission scanning electron microscopy (FE-SEM) in conjunction with X-ray energy-dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD).The morphology of CuO NPs was investigated using the QuantaTM 450 FEG.A SHI-MADZU-IR PRESTIGE-21 Spectrometer was used to identify the functional groups of the CuO NPs.Using Bruker D8 Advance X-ray diffractometer (λ = 1.54 Å, 40 mA, 45 kV) and Cu-Kα radiation, the crystal structure of the CuO NPs was estimated throughout a 20-80° range.

Characterization of CuO NPs
A spectrophotometer (Shimadzu UV-vis V-530A with a wavelength of 200 to 800 nm) was employed to determine the UV-vis absorption spectra of various substances.The synthesized CuO NPs were characterized using several techniques: field emission scanning electron microscopy (FE-SEM) in conjunction with X-ray energy-dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD).The morphology of CuO NPs was investigated using the QuantaTM 450 FEG.A SHIMADZU-IR PRESTIGE-21 Spectrometer was used to identify the functional groups of the CuO NPs.Using Bruker D8 Advance X-ray diffractometer (λ = 1.54 Å, 40 mA, 45 kV) and Cu-Kα radiation, the crystal structure of the CuO NPs was estimated throughout a 20-80 • range.

Adsorption Batch Studies
The MB dye's optimal adsorption performance was achieved by adjusting the CuO NPs dose, contact time, and MB dye concentrations.After combining a weighed sample of CuO NPs with 3.0 milliliters of MB dye solution, the mixture's pH was adjusted.The mixture was stirred at a steady temperature before centrifugation at 150 rpm for a specific duration.By using the JANEWAY 7315 Spectrophotometer (with λmax of 660 nm), the amount of MB dye in the supernatant was determined.Equations ( 1) and ( 2) were used to compute MB adsorption capacity (q) at equilibrium and at time, while Equation (3) was used for computing the dye removal percentage (%R) [38,39].
where C i , C e , and C t denote the MB dye concentration in the initial, at the equilibrium, and at time t (measured in milligrams per liter), respectively.V represents the solution volume in liters.Meanwhile, M refers to the mass of the CuO NPs adsorbent in grams.

Adsorption Kinetics and Isotherms Studies
The kinetics of adsorption provides useful data for adsorption process performance and design which can be applied practically.An investigation was conducted to examine the adsorption mechanism utilizing pseudo-first-order Equation ( 4), pseudo-second-order Equation ( 5), and Elovich Equation ( 6) for kinetic models [40,41].
where t is the time, k 1 (min −1 ), k 2 (g•mg −1 min −1 ) are the rate constants for the pseudofirst-order and the pseudo-second-order models, respectively, α (mg•g −1 ) is the rate of adsorption at initial, and β is the constant of desorption (g•mg −1 ).Adsorption isotherms can be used to examine the relationship between C e and q e of MB at a certain temperature.The adsorption isothermal behavior for CuO NPs was described using three models: Langmuir Equation ( 7), Freundlich Equation ( 8), and Tempkin Equation ( 9) [42,43]. 1 ) where , and A T (L•mg −1 ) are the equilibrium rate constants for Langmuir, Freundlich, and Tempkin, respectively; 1/n represents an empirical constant indicating the adsorption intensity; 1/n is a constant indicating the adsorption intensity.

UV-Visible Adsorption Spectrum
The absorption spectrum of CuO NPs and Melia azedarach fruit extract in the UVvis range has been depicted in Figure 1.The presence of various bioactive compounds, including flavonoids, alkaloids, carbohydrates, tannins, phenolic acid, and terpenoids, in the aqueous fruit extract of Melia azedarach has been attributed to the significant absorption peak observed at 269 nm.These compounds have been identified as being essential for CuO NPs production [36,44].CuO NPs production was shown by the fruit extract's quick color change to green upon the addition of CuCl 2 •2H 2 O solution.The confirmation of the reduction to CuO NPs was established through the observation of a significant absorption peak at 350 nm.This peak is probably connected to the CuO semiconductor excitation's surface plasmon resonance (SPR) [27,45,46].

FE-SEM and EDS
The size and shape of the synthesized CuO NPs were analyzed using FE-SEM micrographs.The FE-SEM micrographs of CuONPs before and after adsorption of MB dye are displayed in the inset of Figure 2a,b; these were captured at a resolution of 500 nm.Based on the FE-SEM image in Figure 2a, the produced CuO NPs displayed a uniform and distinctly spherical structure, though they exhibited some agglomeration due to the adhesive properties of the plant extract [47].After adsorption, as shown in Figure 2b, the surface coverage of the CuO NPs is visible.This coverage is attributed to the adsorption of adsorbate molecules (MB), which is likely what leads to the formation of a monolayer of adsorbate molecules on the adsorbent surface.Image J software (1.48v) was used to measure the particle size of CuO NPs, as shown in Figure 2c.The results showed a particle size range between 20 and 40 nm, indicating the presence of well-established synthetic nanoparticles [48].Additionally, the purity of the synthesized CuO NPs was demonstrated by an EDS spectrum, which was employed to evaluate the elemental analysis, as shown in Figure 2d.The presence of oxygen and copper in the EDS spectrum suggests that the copper is likely in the form of an oxide or dioxide.Copper (Cu) and oxygen (O) had weight compositions of 6.79 and 45.41 percent, respectively.Subsequently, the atomic compositions were determined to be 1.81 percent and 48.19 percent, respectively.Due to interactions with the extract during the bioprocessing, minor amounts of carbon, chloride, and potassium were found.It was confirmed that CuO NPs were precisely created using green synthesis based on the SEM and EDS micrographs [49].Additionally, the purity of the synthesized CuO NPs was demonstrated by an EDS spectrum, which was employed to evaluate the elemental analysis, as shown in Figure 2d.The presence of oxygen and copper in the EDS spectrum suggests that the copper is likely in the form of an oxide or dioxide.Copper (Cu) and oxygen (O) had weight compositions of 6.79 and 45.41 percent, respectively.Subsequently, the atomic compositions were de-termined to be 1.81 percent and 48.19 percent, respectively.Due to interactions with the extract during the bioprocessing, minor amounts of carbon, chloride, and potassium were found.It was confirmed that CuO NPs were precisely created using green synthesis based on the SEM and EDS micrographs [49].

FTIR Spectroscopy
FTIR spectroscopy was utilized to investigate the various functional groups present in the synthesized CuO NPs within the spectral range of 400-4000 cm −1 , as shown in Figure 3a.The presence of phenolic compounds and absorbed water on the surface of CuO NPs is suggested by the bandwidth at (3524 cm −1 ), which is associated with the -OH group stretching frequency [50].Elevated peaks at (2922 cm −1 and 2865 cm −1 ) indicate asymmetric stretching of C-H bonds in -CH 2 and -CH 3 groups, respectively [31,51].
Chemistry 2024, 6, FOR PEER REVIEW 7 Furthermore, Cu-O vibrations can be linked to peaks at (531 cm −1 and 634 cm −1 ), demonstrating the production of CuO nanoparticles [52,55].The bioactive compounds present in Melia azedarach fruit extract have a significant impact on the production of CuO NPs.The FTIR analysis showed that the synthesized CuO NPs have many functional groups.These groups are most reactive to adsorbing MB dye cations through an electrostatic interaction [56].

Effect of pH
The CuO NP adsorption efficiency was examined in MB dye solutions at a concentration (10 mg•L −1 ) and a pH (4 to 8). Figure 4 shows that both the percentage of removal %R and the adsorption capacity (qe) of MB significantly improved when the pH value was raised from 4 to 8. Adsorption sites that are positively charged and open the uptake of anions found in solutions with low pH values.The competitiveness of H + ions and dye cations for the few available adsorption sites may be the cause of the reduced MB adsorption at acidic pH values.The maximum MB adsorption percentage %R was 82.051% at a pH of 8.For the next experiments, pH 8 was chosen because of this.In general, these results are compatible with previous studies [4,59,60].The C=C aromatic bending vibration of alkenes in the Melia azedarach fruit extract is responsible for the strong absorption band that appeared at (1633 cm −1 ) [52,53].The deformation vibration of the alkane group's C-H band is responsible for the sharp peak at (1406 cm −1 ).The presence of various organic functional groups such as ethers, amides, and other aliphatic groups on the surface of CuO NPs is demonstrated by the peaks observed at (1244 cm −1 and 1075 cm −1 ).The absorption peak observed in primary and secondary alcohols at (1020 cm −1 ) is due to the stretching vibration of the C-O group [54].
Furthermore, Cu-O vibrations can be linked to peaks at (531 cm −1 and 634 cm −1 ), demonstrating the production of CuO nanoparticles [52,55].The bioactive compounds present in Melia azedarach fruit extract have a significant impact on the production of CuO NPs.The FTIR analysis showed that the synthesized CuO NPs have many functional groups.These groups are most reactive to adsorbing MB dye cations through an electrostatic interaction [56]., respectively.The presence of sharpened and well-defined scattering peaks serves as strong evidence supporting the crystalline nature of the CuO nanoparticles, indicating their purity without impurities.The obtained diffraction data closely matched the information recorded in the JCPDS card no.801268 [57,58].

Effect of pH
The CuO NP adsorption efficiency was examined in MB dye solutions at a concentration (10 mg•L −1 ) and a pH (4 to 8). Figure 4 shows that both the percentage of removal %R and the adsorption capacity (q e ) of MB significantly improved when the pH value was raised from 4 to 8. Adsorption sites that are positively charged and open the uptake of anions found in solutions with low pH values.The competitiveness of H + ions and dye cations for the few available adsorption sites may be the cause of the reduced MB adsorption at acidic pH values.The maximum MB adsorption percentage %R was 82.051% at a pH of 8.For the next experiments, pH 8 was chosen because of this.In general, these results are compatible with previous studies [4,59,60].

Effect of CuO NPs Dose
The utilized amount of CuO NPs adsorbent had a considerable impact on the effectiveness of adsorption.CuO NPs adsorbent doses ranging from 0.01 to 0.09 g were employed to investigate the adsorption of MB dye [61,62].Figure 5 depicts the effects of adsorbent dose on MB adsorption.The typical pattern of quickly rising %R as the adsorbent dose increased was followed and equilibrium was attained at 0.09 g with a maximum %R of 93.800%.This was associated with a rise in adsorption-active sites with an increase in dosage, both the adsorbent outer layer and the expanded adsorption sites number, leading to enhanced efficiency in %R.However, the qe value decreased with increasing the adsorbent dose.The existence of more active sites on the surface of CuO NPs may be the cause of the observed drop in adsorption (qe) when doses were high, and the ensuing decrease in accessible MB molecules for adsorption [17,63].Consequently, 0.05 g of CuO NPs was chosen for subsequent studies based on the findings of the dose experiment.

Effect of CuO NPs Dose
The utilized amount of CuO NPs adsorbent had a considerable impact on the effectiveness of adsorption.CuO NPs adsorbent doses ranging from 0.01 to 0.09 g were employed to investigate the adsorption of MB dye [61,62].Figure 5 depicts the effects of adsorbent dose on MB adsorption.The typical pattern of quickly rising %R as the adsorbent dose increased was followed and equilibrium was attained at 0.09 g with a maximum %R of 93.800%.This was associated with a rise in adsorption-active sites with an increase in dosage, both the adsorbent outer layer and the expanded adsorption sites number, leading to enhanced efficiency in %R.However, the q e value decreased with increasing the adsorbent dose.The existence of more active sites on the surface of CuO NPs may be the cause of the observed drop in adsorption (q e ) when doses were high, and the ensuing decrease in accessible MB molecules for adsorption [17,63].Consequently, 0.05 g of CuO NPs was chosen for subsequent studies based on the findings of the dose experiment.

Effect of CuO NPs Dose
The utilized amount of CuO NPs adsorbent had a considerable impact on the effectiveness of adsorption.CuO NPs adsorbent doses ranging from 0.01 to 0.09 g were employed to investigate the adsorption of MB dye [61,62].Figure 5 depicts the effects of adsorbent dose on MB adsorption.The typical pattern of quickly rising %R as the adsorbent dose increased was followed and equilibrium was attained at 0.09 g with a maximum %R of 93.800%.This was associated with a rise in adsorption-active sites with an increase in dosage, both the adsorbent outer layer and the expanded adsorption sites number, leading to enhanced efficiency in %R.However, the qe value decreased with increasing the adsorbent dose.The existence of more active sites on the surface of CuO NPs may be the cause of the observed drop in adsorption (qe) when doses were high, and the ensuing decrease in accessible MB molecules for adsorption [17,63].Consequently, 0.05 g of CuO NPs was chosen for subsequent studies based on the findings of the dose experiment.

Effect of Contact Time and Kinetic Study
Figure 6a displays the UV-vis spectra of the MB absorption at various times (5-120 min) after being adsorbed by the CuO NPs.The uniqueness of the adsorption process is evident from the consistent decrease in absorbance intensity without any changes in wavelength throughout the adsorption [7,64].
tional insight into the features of the adsorption process [2,5,66].Kinetic parameter re for these three models are listed in Table 1.
According to the data presented (Table 1), the correlation coefficient R 2 value o pseudo-second-order kinetic model (0.9925) is much higher than that of the pseudo order (0.8533) and Elovich (0.8944) kinetic models.This indicated that the pseudo-se order model provided a more precise description of the adsorption kinetics of MB Additionally, there was a high level of agreement between the experimental value (0.9723) and the calculated value (qe)cal.(0.9971) for the pseudo-second-order kinetic m This finding serves as evidence of the precision of the model [68].As compared to models, the pseudo-second-order kinetic model exhibited better performance in remo MB dye from solutions using CuO NPs [38,69,70].Figure 6b illustrates the effects of time on MB adsorption onto CuO NPs.As the adsorption duration increased, the MB's adsorption capacity (q e ) and removal percentage %R both rose until they reached equilibrium after 120 min.At equilibrium, the q e for MB was established to be 0.96 (mg•g −1 ), while the corresponding %R was determined to be 80.598% [65].
Experimental data from batch studies were fitted with the pseudo-first-order Figure 7a, pseudo-second-order Figure 7b, and Elovich Figure 7c kinetic models to assess the adsorption kinetics of MB under the optimal adsorption conditions and provide additional insight into the features of the adsorption process [2,5,66].Kinetic parameter results for these three models are listed in Table 1.According to the data presented (Table 1), the correlation coefficient R 2 value of the pseudo-second-order kinetic model (0.9925) is much higher than that of the pseudo-firstorder (0.8533) and Elovich (0.8944) kinetic models.This indicated that the pseudo-secondorder model provided a more precise description of the adsorption kinetics of MB [67].Additionally, there was a high level of agreement between the experimental value (q e ) exp. (0.9723) and the calculated value (q e ) calc.(0.9971) for the pseudo-second-order kinetic model.This finding serves as evidence of the precision of the model [68].As compared to other models, the pseudo-second-order kinetic model exhibited better performance in removing MB dye from solutions using CuO NPs [38,69,70].

Effect of Initial Concentration and Isotherms Study
Figure 8 shows that CuO NPs' adsorption capacity (q e ) and removal percentage (%R) are significantly influenced by the initial MB concentration (C i ).When the C i increased, the %R remained constant from 81.026% to 85.869%, while the q e values of the CuO NPs increased by 0.498, 0.972, 1.546, 2.027, and 2.497 mg•g −1 for concentrations of 10, 20, 30, 40, and 50 mg•L −1 , respectively.This can be attributed as the C i increased, the resistance to MB mass transferring across solid phases and aqueous phases is overcome, resulting in increased sorption.Furthermore, when the MB concentration rose, the interaction between MB and the CuO NPs was enhanced, accelerating the sorption process [71,72].Other studies conducted by different researchers have reported comparable findings concerning the influence of the initial MB concentration [73,74].

Effect of Initial Concentration and Isotherms Study
Figure 8 shows that CuO NPs' adsorption capacity (qe) and removal percentage (%R) are significantly influenced by the initial MB concentration (Ci).When the Ci increased, the %R remained constant from 81.026% to 85.869%, while the qe values of the CuO NPs increased by 0.498, 0.972, 1.546, 2.027, and 2.497 mg•g −1 for concentrations of 10, 20, 30, 40, and 50 mg•L −1 , respectively.This can be attributed as the Ci increased, the resistance to MB mass transferring across solid phases and aqueous phases is overcome, resulting in increased sorption.Furthermore, when the MB concentration rose, the interaction between MB and the CuO NPs was enhanced, accelerating the sorption process [71,72].Other studies conducted by different researchers have reported comparable findings concerning the influence of the initial MB concentration [73,74].An adsorption isotherm describes the distribution of adsorbate molecules between the liquid and solid phases once the adsorption process has reached equilibrium.In cases where the adsorption surface is homogeneous and the affinity of the adsorbate is the same at each adsorption site, the Langmuir isotherm is often the most appropriate model to use An adsorption isotherm describes the distribution of adsorbate molecules between the liquid and solid phases once the adsorption process has reached equilibrium.In cases where the adsorption surface is homogeneous and the affinity of the adsorbate is the same at each adsorption site, the Langmuir isotherm is often the most appropriate model to use [75].The Freundlich isotherm model was developed specifically for heterogeneous systems and describes multilayer adsorption occurring on the sorbent surface [76].According to the Temkin isotherm, as adsorbate coverage increases, the heat of adsorption of each molecule in the layer drops linearly [77].Figure 9a-c 2, the Langmuir isotherm model was found to hav a significantly higher correlation coefficient (R 2 = 0.9754) with the adsorption of MB b CuO NPs compared to other isotherm models.This value proves that the parameter an the confirmation of monolayer adsorption of MB onto CuO NPs are in good agreemen [78].The value of Qm indicates how much MB dye is needed for every unit weight o sorbent to form a full monolayer on the CuO NPs surface.Table 3 shows the CuO NP adsorption capacity Qm for MB dye adsorption compared to different types of adsorben in the previous studies.After examining the data in Table 2, the Langmuir isotherm model was found to have a significantly higher correlation coefficient (R 2 = 0.9754) with the adsorption of MB by CuO NPs compared to other isotherm models.This value proves that the parameter and the confirmation of monolayer adsorption of MB onto CuO NPs are in good agreement [78].The value of Q m indicates how much MB dye is needed for every unit weight of sorbent to form a full monolayer on the CuO NPs surface.Table 3 shows the CuO NPs' adsorption capacity Q m for MB dye adsorption compared to different types of adsorbents in the previous studies.Additionally, the Freundlich isotherm's n value provides a clear indication of the adsorption behavior.Generally, the adsorption is classified as (i) chemical, (ii) physical, or (iii) linear depending on whether n is less than, greater than, or equal to one [87,88].Physical adsorption outperforms chemical adsorption in the case of CuO NPs since the value of n is greater than one (1.042).Furthermore, the value of 1/n (0.960) falls within the range 0 < 1/n < 1, demonstrating that the adsorption process is favorable [89].The adsorption of dyes involves numerous mechanisms, including ion exchange, hydrogen bonding, Van der Waals forces, electrostatics, and dipole-ion interaction.According to the kinetic and isotherm data, the adsorption mechanism of MB onto CuO NPs is mainly based on physical attraction.Therefore, it can be suggested that electrostatic interactions are the main mechanism of adsorption [90].

Conclusions
It can be concluded that the aqueous extract from Melia azedarach fruit was successfully used to synthesize CuO NPs utilizing the green route approach.The bioactive compounds in Melia azedarach's aqueous fruit extract can serve as a reducing agent to synthesize the CuO NPs.The prepared particles were spherical in morphology and ranged in size from 20 to 40 nm on average.According to the results, CuO nanoparticles show great promise for successfully removing MB dye from aqueous solutions.The optimum conditions for the elimination of MB dye were pH (8), adsorbent dosage (0.05 g), initial MB concentration (20 mg•L −1 ), and a period of 120 min.The pseudo-second-order kinetic model accurately described the adsorption process.Furthermore, the values of the calculated adsorption capacity (q e ) calc.(0.9971) and the experimental adsorption capacity (q e ) exp. (0.9723) exhibits good agreement.The Langmuir isotherm offered a good fit to the data and the maximum adsorption capacity toward MB was 26.738 mg•g −1 .

Figure 1 .
Figure 1.UV-visible spectra of plant extract and CuO NPs.

Figure 1 .
Figure 1.UV-visible spectra of plant extract and CuO NPs.

Figure 4 .
Figure 4. pH effect on MB adsorption by CuO NPs.

Figure
Figure 6a displays the UV-vis spectra of the MB absorption at various times (5-120 min) after being adsorbed by the CuO NPs.The uniqueness of the adsorption process is

Figure 4 .
Figure 4. pH effect on MB adsorption by CuO NPs.

Figure 4 .
Figure 4. pH effect on MB adsorption by CuO NPs.

Figure
Figure 6a displays the UV-vis spectra of the MB absorption at various times (5-120 min) after being adsorbed by the CuO NPs.The uniqueness of the adsorption process is

Figure 6 .
Figure 6.(a) UV-vis spectra of MB adsorption by CuO NPs at different times; (b) contact time on MB adsorption.

Figure 6 .
Figure 6.(a) UV-vis spectra of MB adsorption by CuO NPs at different times; (b) contact time effect on MB adsorption.
depicts the linear models used to study the interactions of MB on the CuO NP surface.Table2displays the computed values of the parameters in the Langmuir, Freundlich, and Tempkin equations.

Chemistry 2024, 6 ,Figure 9 .
Figure 9. (a) Langmuir, (b) Freundlich, and (c) Tempkin adsorption isotherms for adsorption of M After examining the data in Table2, the Langmuir isotherm model was found to hav a significantly higher correlation coefficient (R 2 = 0.9754) with the adsorption of MB b CuO NPs compared to other isotherm models.This value proves that the parameter an the confirmation of monolayer adsorption of MB onto CuO NPs are in good agreemen[78].The value of Qm indicates how much MB dye is needed for every unit weight o sorbent to form a full monolayer on the CuO NPs surface.Table3shows the CuO NP adsorption capacity Qm for MB dye adsorption compared to different types of adsorben in the previous studies.

Table 1 .
Kinetic parameters result from the adsorption of MB onto CuO NPs.

Table 1 .
Chemistry 2024, 6, FOR PEER REVIEW 11 Kinetic parameters result from the adsorption of MB onto CuO NPs.

Table 3 .
The adsorption capacities Qm for different types of MB adsorbents in the previous studies

Table 2 .
Results of the adsorption isotherms parameters for MB adsorption onto CuO NPs.

Table 3 .
The adsorption capacities Q m for different types of MB adsorbents in the previous studies.