Bio-Zirconium Metal–Organic Framework Regenerable Bio-Beads for the Effective Removal of Organophosphates from Polluted Water

Organophosphate-based pesticides, such as diazinon, are among the most toxic organic contaminants to human and environment. Effective removal of diazinon from contaminated water sources is critical. Zirconium Metal−organic frameworks (Zr-MOFs) are promising candidates for the removal of organic contaminants from wastewater. Herein, we report the adequacy of a bio based Zr-MOF named MIP-202 for the removal of diazinon from water. On the other hand, the use of these materials in powder form is not workable, the development of scalable and economical processes and integrative of these materials onto beads is paramount for industrial processes. Hence, it was reported a scalable, bio aqueous solution-based preparation strategy for Bio Zr-MOF beads production. The composite material exposed identical reactivity under the same ambient parameters compared to powdered material in an aqueous solution. These results signify a critical procedure to an integrated strategy for organophosphates removal using bio-based MOFs, which demonstrates high potential for manufacturing applications such as continued removal of organophosphates from wastewater supplies.


Introduction
Agriculture and industrial manufacturing have contaminated freshwater sources with numerous inorganic and organic pollutants [1,2]. Finding ways to effectively alleviate this pollution is of paramount importance to protect and improve human, animal, environment, and aquatic life [3]. Organophosphate pesticides such as diazinon are one of the most famous organic contaminants in water supplies [4][5][6]. Diazinon is considered one of the parent MOFs, resulting in low loading efficiency or not being biocompatible [38]. In addition, it is still challenging to prepare MOFs compounds that provide high surface area and fulfillment similar to the major MOFs using green strategies to get an industrial applicable form of MOFs powder [39]. For this, it was reported here a facile and scalable strategy for the synthesis of millimeter-sized bio-Zr MOF composite beads that are constructed from chitosan and sodium alginate in form of biocompatible beads, named chitosan-alginate beads (CA). Chitosan and alginate are considered one of the most widely used biomaterials [40]. Here, we used this method to formulate MIP-202 MOF powder in the form of processable beads. The adsorption performance of the fabricated MIP-202/CA beads has been investigated for diazinon remediation from waste solutions.

Synthesis of MIP-202 Powder
MIP-202 powder was synthesized using a modified green method to obtain colloidal stable nanoparticles. It is worth mentioning that MIP-202 is prepared without using any organic solvents that commonly used for MOFs synthesis. MIP-202 was synthesized by mixing ZrCl 4 (1.15 g, 4.93 mmol) and L-aspartic acid (1.4 g, 10.52 mmol) and completely dissolving them in deionized water (10 mL). Then, the solution was transferred into a 100 mL round flask and refluxed at 90 • C under continuous stirring for 24 h. subsequently, the solution was kept out to cool down at room temperature and then washed several times with ethanol. Finally, the resulting precipitate was isolated and centrifuged to obtain the resulting precipitate. The white powder was collected and dried in a vacuum oven at room temperature for 24 h.

Fabrication of MIP-202/CA Beads Composite
One gram of MIP-202 was dispersed in a 100 mL of sodium alginate aqueous solution under stirring as indicated in Figure 1. Meanwhile, the curing solution was synthesized via dissolving 0.6 g of anhydrous CaCl 2 in 100 mL of 0.1 mol/L chitosan aqueous solution. Then, the sodium alginate aqueous solution was dropped into the processing solution. After modelling (Figure 1), the collected synthetic beads were washed several times by distilled water. This followed by a freeze-drying step to produce the composite MIP-202/CA spherical beads. The chemical structures of the formulated beads MIP-202/CA composite is identified in Figure 1.

Characterization Methods
Powder X-ray diffraction (PXRD) analysis were done using a D8 Bruker X-ray powder diffractometer, (CuKα1 radiation, λ = 1.54056 Å) at 40 kV and 40 mA and intensity data for 2θ from 20 • to 70 • over a period of 30 min. Fourier-transform infrared spectroscopy (FTIR) spectra were produced using Bruker Vertex 70 to explore chemical properties of MIP-202 after and before polymeric blend immobilization. Scanning electron microscopy (SEM) images were investigated using a Hitachi isotherms collected at 77 K by a Micromeritics Tristar II 3020. Thermal stability of the samples were performed using thermogravimetric analysis (TGA) as the samples were heated room temperature-700 • C with a rate of 10 • C/min under a constant flow of air. Freeze drying was performed with a critical point freeze dryer. Briefly, freeze drying was used in activation the water-soaked samples over a period of eight hours.

Characterization Methods
Powder X-ray diffraction (PXRD) analysis were done using a D8 Bruker X-ray powder diffractometer, (CuKα1 radiation, λ = 1.54056 Å) at 40 kV and 40 mA and intensity data for 2θ from 20° to 70° over a period of 30 min. Fourier-transform infrared spectroscopy (FTIR) spectra were produced using Bruker Vertex 70 to explore chemica properties of MIP-202 after and before polymeric blend immobilization. Scanning electron microscopy (SEM) images were investigated using a Hitachi SU8030 FE-SEM (Dallas, TX USA) microscope. The samples images were performed by transmission electron microscope (TEM) JEOL JEM-2100 200 kV (JEOL, Ltd. Akishima, Tokyo, Japan) by drop casting the MIP-202 powder and grounded MIP-202/CA composited beads and ethano onto the 200-mesh copper TEM grid. The apparent surface areas were determined from nitrogen adsorption-desorption isotherms collected at 77 K by a Micromeritics Tristar I 3020. Thermal stability of the samples were performed using thermogravimetric analysis (TGA) as the samples were heated room temperature-700 °C with a rate of 10 °C/min under a constant flow of air. Freeze drying was performed with a critical point freeze dryer. Briefly, freeze drying was used in activation the water-soaked samples over a period of eight hours.

Batch Adsorption of Diazinon from Polluted Water via MIP-202/CA Composite Beads
The diazinon adsorption efficiency of the MIP-202 bio-MOF/CA beads were investigated using batch technique. In batch method, 100 mg of different materials (MIP 202 bio-MOF, CA net beads, and MIP-202/CA composite beads) was mixed with 100 mL of 50 ppm diazinon solution concentration of pH = 7 at 22 °C for various time intervals (0-90 min) using a shaking incubator (Yellow line, Germany). The influence of processing parameters on the adsorption behavior of the MIP-202/CA beads including MIP-202/CA beads dosage (0.1-4.0 g/L), and initial pollutant concentration (10-100 ppm) were The diazinon adsorption efficiency of the MIP-202 bio-MOF/CA beads were investigated using batch technique. In batch method, 100 mg of different materials (MIP-202 bio-MOF, CA net beads, and MIP-202/CA composite beads) was mixed with 100 mL of 50 ppm diazinon solution concentration of pH = 7 at 22 • C for various time intervals (0-90 min) using a shaking incubator (Yellow line, Germany). The influence of processing parameters on the adsorption behavior of the MIP-202/CA beads including MIP-202/CA beads dosage (0.1-4.0 g/L), and initial pollutant concentration (10-100 ppm) were constituted. The accuracy of the data was proved by repeating all tests in triplicate and it was used the mean average values in the analysis processes.

Analytical Methods
After the diazinon adsorption processes, the adsorbent materials were separated using the centrifuge to control the final diazinon concentration via high-performance liquid chromatography (HPLC, Shimadzu, Japan). Subsequently, the supernatants were filtered using 0.25 µm syringe filters before injection into C18 column. The mobile phase was a mixture of methanol (88%) and ultrapure water (12%). The injection volume of diazinon solution was 20 µL. The flow rate and temperature of operation were 1 mL/min and 30 • C, respectively. Additionally, the detection wavelength of diazinon was 254 nm. Furthermore, the intermediate products of diazinon were set using liquid chromatography tandem mass spectroscopy (LC-MS/MS) analysis. A mixture of 65% methanol: 35% of 0.1% formic acid was utilized to detect the intermediates products of diazinon. The analysis experiments were done at flow rate and temperature of 0.4 mL/min and 35 • C, respectively.
The diazinon removal percentage via the adsorbent materials was determined from Equation (1) [40]. where, C o is the initial diazinon concentration (mg/L); and C e is the diazinon concentration at equilibrium in aqueous solution (mg/L). The adsorption capacity (mg/g) of the diazinon was calculated by Equation (2) [40]: where, V is the diazinon solution volume (L); and m is the mass of adsorbent material (g).

Equilibrium Isotherm Analysis for Diazinon Adsorption onto MIP 202/CA Composite Beads
Langmuir, Freundlich, and Temkin models were used to explain the performance of the adsorption processes of diazinon onto synthesized MIP-202 bio-MOF/CA beads. The Langmuir equation can be presented as following: where, q e (mg/g) is the adsorbed amount of diazinon at equilibrium; C e (mg/L) is the concentration of the adsorbate at equilibrium; and q m (mg/g) and K L (L/mg) are Langmuir constants referred to the maximum monolayer adsorption capacity and adsorption energy, respectively. Moreover, the following Freundlich linear equation was applied to analyze the equilibrium data, by plotting log q e versus log C e .
Log q e = log K F + 1/n F log C e where K F and n F are Freundlich constants related to the adsorption capacity and intensity, respectively. Temkin isotherm model was expressed for the adsorption behavior of diazinon onto the fabricated MIP-202 bio-MOF/CA beads as following [40].
where, A (L/g) is the Temkin constant; and B = RT/b (J/mol) is constant referred to adsorption heat.

Kinetic Models for Diazinon Adsorption onto MIP 202 Bio-MOF/CA Beads
To examine the diazinon adsorption technique on MIP-202 bio-MOF/CA composite beads from wastewater, the pseudo-first order, pseudo-second order, Elovich, and intraparticle diffusion kinetic models were utilized. The Lagergren first-order equation is represented as follows: ln (q e − q t ) = ln q e − k 1 t where, q e and q t (mg/g) are the amounts of adsorbed diazinon at equilibrium and at time t (min), respectively. k 1 (min) expresses the constant rate of the first-order kinetic model. Moreover, the pseudo-second order kinetic model was used to analyze the adsorption kinetic data which can be expressed as following: where, k 2 (g/mg·min) is the constant of the second-order rate. Furthermore, the following equation express Elovich model: where, α is (mg/g·min) the initial adsorption rate and β (g/mg) refers to the degree of the surface concealment and physical activation energy of adsorption. α and β can be obtained by calculating the slope and interrupt of the linear plot of q t against ln t, respectively. In a similar manner, the intraparticle diffusion affecting the diazinon adsorption processes from aqueous solution was expressed using Weber and Morris equation; where, k i is the intraparticle diffusion rate constant. The value of C gives prediction about the boundary layer thickness. If intraparticle diffusion occurs, q t vs. t 0.5 is linear and if the plot cross through the origin, the rate determination is only due to the intraparticle diffusion.

Reusability Study of the Fabricated MIP-202/CA Composite Beads
To evaluate the economic feasibility of the fabricated MIP-202 bio-MOF/CA beads in water treatment processes, the adsorption-desorption cycle was repeated for five times, where the adsorbent material was washed with distilled water and ethanol then dried in air for to be reused.

Optimization and Characterizations of MIP-202 Nanopwders and MIP-202/CA Beads Composite
MIP-202 MOF was selected as a bio-based zirconium MOF for the removal of diazinon from wastewater. MIP-202 is constructed from zirconium metal and aspartic acid through strong Zr(IV)−O bonds in which the 12-connected Zr 6 (µ 3 -O)4(µ 3 -OH) 4 node and the L-aspartate ligand which explain extraordinary water stabilization due to Zr(IV)−O bonds [35]. So, MIP-202 has been investigated previously for the removal of dyes and heavy metals from the polluted water [36]. As, MIP-202 MOF material was produced using modified green technique, so its bulk phase purity was assured by the experimental PXRD as indicated from Figure      In addition, the colloidal stability of the prepared MIP-202 particles was attained as shown from DLS measurements and zeta potential ( Figure 4). The size of MIP-202 nanoparticles is proven by DLS and it shows a good agreement with the particle size measured from TEM images. It is interesting to note that the resulting MIP-202 nanoparticles powder showed high colloidal stability in water for several days. This is attributed to the high positive charge on MIP-202 nanoparticles measured using zeta potential with a value of 41.4 mv as shown in Figure 4. This high positive value of zeta potential allowed the nanoparticles of MIP-202 to be colloidally stable due to repulsion between particles in solution for several days as shown in Figure 1. The high colloidal stability of these nanoparticles prevents the sedimentation of MIP-202 particles while mixing the solution with alginate polymer solution which provided proper mixing, distribution, and incorporation of MIP-202 powder with alginate powder to provide an efficient mixed matrix of polymer and MIP-202 nanoparticles. The homogeneous distribution of MIP-202 nano-powder onto the CA polymeric blend was confirmed through imaging examination.
nanoparticles powder showed high colloidal stability in water for several days. This is attributed to the high positive charge on MIP-202 nanoparticles measured using zeta potential with a value of 41.4 mv as shown in Figure 4. This high positive value of zeta potential allowed the nanoparticles of MIP-202 to be colloidally stable due to repulsion between particles in solution for several days as shown in Figure 1. The high colloidal stability of these nanoparticles prevents the sedimentation of MIP-202 particles while mixing the solution with alginate polymer solution which provided proper mixing, distribution, and incorporation of MIP-202 powder with alginate powder to provide an efficient mixed matrix of polymer and MIP-202 nanoparticles. The homogeneous distribution of MIP-202 nano-powder onto the CA polymeric blend was confirmed through imaging examination.   MIP-202 powder and MIP-202/CA composite beads was conducted using TGA ( Figure 5). It is clear that both materials attain high thermal stability as both materials showed stability till 260 • C. For MIP-202 pristine powder, it shows first step thermal degradation of 12% weight loss at 100 • C, this is attributed to the release of adsorbed moisture and solvent adsorbed on the surface structure of the MOF. The same degradation step is observed in case of MIP-202/CA of weight loss around 12% but at 120 • C. The MIP-202/CA composite demonstrates second degradation step from 120 • C to 260 • C due to the release of water and residual solvent from the internal pores of MOF. The pristine MIP-202 shows also a second weight loss step from 100 • C to 260 • C due to the same reason. A gradual weight loss is observed for both pristine MIP-202 and MIP-202/CA after 260 • C to 700 • C due to the degradation of aspartic acid ligand and chitosan and alginate polymer in case of MIP-202/CA composite. A total weight loss of 60% is observed for both pristine MIP-202 and MIP-202/CA at 700 • C. 202/CA composite demonstrates second degradation step from 120 °C to 260 °C due to the release of water and residual solvent from the internal pores of MOF. The pristine MIP-202 shows also a second weight loss step from 100 °C to 260 °C due to the same reason. A gradual weight loss is observed for both pristine MIP-202 and MIP-202/CA after 260 °C to 700 °C due to the degradation of aspartic acid ligand and chitosan and alginate polymer in case of MIP-202/CA composite. A total weight loss of 60% is observed for both pristine MIP-202 and MIP-202/CA at 700 °C. The nitrogen sorption isotherms of the resulting beads exhibited a detention of the porosity of MIP-202 embedded within the CA beads. The calculated BET surface areas was 180 m 2 /g for MIP-202 powder and 160 m 2 /g for MIP-202/CA composite beads, respectively, as evident from Figure 6. Moreover, the total pore volume and mean pore diameters were measured to be 0.061 cm 3 /g and 2.52 nm for the free MIP-202 powder, respectively. These values were estimated to be 0.029 cm 3 /g for the total pore volume and 12.24 nm for the average pore diameters of MIP-202/CA composite beads. The nitrogen sorption isotherms of the resulting beads exhibited a detention of the porosity of MIP-202 embedded within the CA beads. The calculated BET surface areas was 180 m 2 /g for MIP-202 powder and 160 m 2 /g for MIP-202/CA composite beads, respectively, as evident from Figure 6. Moreover, the total pore volume and mean pore diameters were measured to be 0.061 cm 3 /g and 2.52 nm for the free MIP-202 powder, respectively. These values were estimated to be 0.029 cm 3 /g for the total pore volume and 12.24 nm for the average pore diameters of MIP-202/CA composite beads.

Diazinon Decontamination Using the Fabricated MIP-202/CA Composite Beads
The diazinon adsorption feasibility onto the fabricated MIP-202/CA composite beads from waste solutions onto the synthesized materials was performed using batch technique at room temperature. Figure 7 demonstrates the influence of contact time of the diazinon adsorption percentage for the prepared MIP-202 bio-MOF powder, CA neat bio-beads, and MIP-202/CA composite beads at a time 0-90 min. It was observed that the neat CA bio-beads achieved the lowest adsorption performance of diazinon compared to MIP-202 powder and its composite beads. It is illustrated that, with increasing the contact time till the equilibrium state, the removal efficiency of diazinon onto the synthesized materials increased. The high diazinon adsorption rate in the first phase may be attributed to the functional groups and high surface area of the adsorbent materials which is binding with the diazinon molecule. The MIP-202/CA composite beads was recomended as an optimum adsorbent material for the supplementary experiments. The optimum contact time of the diazinon removal processes is recorded at 40 min, and the maximum diazinon adsorption percentage is 75.62%. At the second phase of adsorption, all active places of the adsorbent materials were saturated with diazinon molecules and non-significant adsorption results were achieved.

Diazinon Decontamination Using the Fabricated MIP-202/CA Composite Beads
The diazinon adsorption feasibility onto the fabricated MIP-202/CA composite beads from waste solutions onto the synthesized materials was performed using batch technique at room temperature. Figure 7 demonstrates the influence of contact time of the diazinon adsorption percentage for the prepared MIP-202 bio-MOF powder, CA neat bio-beads, and MIP-202/CA composite beads at a time 0-90 min. It was observed that the neat CA bio-beads achieved the lowest adsorption performance of diazinon compared to MIP-202 powder and its composite beads. It is illustrated that, with increasing the contact time till the equilibrium state, the removal efficiency of diazinon onto the synthesized materials increased. The high diazinon adsorption rate in the first phase may be attributed to the functional groups and high surface area of the adsorbent materials which is binding with the diazinon molecule. The MIP-202/CA composite beads was recomended as an optimum adsorbent material for the supplementary experiments. The optimum contact time of the diazinon removal processes is recorded at 40 min, and the maximum diazinon adsorption percentage is 75.62%. At the second phase of adsorption, all active places of the adsorbent materials were saturated with diazinon molecules and non-significant adsorption results were achieved.

Influence of MIP-202/CA Composite Beads Dosage on the Diazinon Adsorption Processes
One of the most significant factors in the adsorption processes for MIP-202/CA composite beads is the dosage due to its influences on the adsorbent beads' capacity. The effect of the prepared MIP-202/CA beads dosage on the diazinon adsorption processes was evaluated after 40 min. Figure 8 illustrates that the diazinon adsorption process was improved as the amount of the synthesized MIP-202/CA beads increased from 0.10 to 4 g/L. conversely, the adsorption capacities of MIP-202/CA beads were decreased with increasing the dosage of adsorbent beads. This decline in the material adsorption capacity of diazinon at high beads dosage may be attributed to the unsaturated places of the MIP-

Influence of MIP-202/CA Composite Beads Dosage on the Diazinon Adsorption Processes
One of the most significant factors in the adsorption processes for MIP-202/CA composite beads is the dosage due to its influences on the adsorbent beads' capacity. The effect of the prepared MIP-202/CA beads dosage on the diazinon adsorption processes was evaluated after 40 min. Figure 8 illustrates that the diazinon adsorption process was improved as the amount of the synthesized MIP-202/CA beads increased from 0.10 to 4 g/L. conversely, the adsorption capacities of MIP-202/CA beads were decreased with increasing the dosage of adsorbent beads. This decline in the material adsorption capacity of diazinon at high beads dosage may be attributed to the unsaturated places of the MIP-202 bio-MOF/CA beads [36]. On the other hand, the dosage increase of MIP-202/CA beads improves the availability of more active sites for diazinon adsorption which enhances the removal ratio of diazinon. Thus, the optimum dosage of MIP-202 bio-MOF/CA beads was chosen as 0.5 g, which is determined as an economical dosage for the diazinon adsorption processes onto the fabricated beads [41]. 202 bio-MOF/CA beads [36]. On the other hand, the dosage increase of MIP-202/CA beads improves the availability of more active sites for diazinon adsorption which enhances the removal ratio of diazinon. Thus, the optimum dosage of MIP-202 bio-MOF/CA beads was chosen as 0.5 g, which is determined as an economical dosage for the diazinon adsorption processes onto the fabricated beads [41].

Influence of Initial Concentrations of Diazinon on the Adsorption Processes
The effect of diazinon initial concentrations was examined after 40 min with the initial concentration starting from 5 to 100 ppm in existence of 0.5 g as an optimum material dosage. In a similar manner, Figure 9 demonstrates that the diazinon adsorption capacities were enhanced with increasing the initial concentrations of diazinon from 10 to 100 ppm, which matched our reported studies [35,41]. This may be attributed to the saturation of the active regons of the MIP-202/CA composite beads increasing the initial diazinon concentrations. Accordingly, it was obvious that the MIP-202/CA beads is efficient as adsorbent agent for diazinon decontamination from waste solutions at different initial concentrations.

Influence of Initial Concentrations of Diazinon on the Adsorption Processes
The effect of diazinon initial concentrations was examined after 40 min with the initial concentration starting from 5 to 100 ppm in existence of 0.5 g as an optimum material dosage. In a similar manner, Figure 9 demonstrates that the diazinon adsorption capacities were enhanced with increasing the initial concentrations of diazinon from 10 to 100 ppm, which matched our reported studies [35,41]. This may be attributed to the saturation of the active regons of the MIP-202/CA composite beads increasing the initial diazinon concentrations. Accordingly, it was obvious that the MIP-202/CA beads is efficient as adsorbent agent for diazinon decontamination from waste solutions at different initial concentrations.
improves the availability of more active sites for diazinon adsorption which enhances the removal ratio of diazinon. Thus, the optimum dosage of MIP-202 bio-MOF/CA beads was chosen as 0.5 g, which is determined as an economical dosage for the diazinon adsorption processes onto the fabricated beads [41].

Influence of Initial Concentrations of Diazinon on the Adsorption Processes
The effect of diazinon initial concentrations was examined after 40 min with the initial concentration starting from 5 to 100 ppm in existence of 0.5 g as an optimum material dosage. In a similar manner, Figure 9 demonstrates that the diazinon adsorption capacities were enhanced with increasing the initial concentrations of diazinon from 10 to 100 ppm, which matched our reported studies [35,41]. This may be attributed to the saturation of the active regons of the MIP-202/CA composite beads increasing the initial diazinon concentrations. Accordingly, it was obvious that the MIP-202/CA beads is efficient as adsorbent agent for diazinon decontamination from waste solutions at different initial concentrations.

Equilibrium Isotherm Analysis for Diazinon Adsorption onto MIP 202/CA Composite Beads
The behaviors of adsorption processes of diazinon onto MIP-202/CA beads were investigated by Langmuir, Freundlich, and Temkin equilibrium models as indicated in Figure 10. Comparing the correlation coefficient of the three studied models at Table 1, it was demonstrated that Langmuir and Temkin models are the most fitted models for description the adsorption processes of diazinon onto the synthesized MIP-202/CA beads. In addition, the separation factor value (R L ) in the range 0 to 1 illustrates the favorable adsorption processes of diazinon via Langmuir model [42]. However, the recorded Freundlich adsorption intensity value (n F ) is 0.357, which is less than the unity, proving that the adsorption process of diazinon onto MIP-202/CA composite beads is unfavorable. On the other hand, the high value of Temkin correlation coefficient demonstrates that the equilibrium data of diazinon adsorption onto the synthesized composite bio-beads are fitted with Temkin isothermal model. Consequently, the Langmuir and Temkin models are the best favorable models for representing the monolayer chemical adsorption of diazinon on the fabricated MIP-202/CA composite beads.

Equilibrium Isotherm Analysis for Diazinon Adsorption onto MIP 202/CA Composite Beads
The behaviors of adsorption processes of diazinon onto MIP-202/CA beads were investigated by Langmuir, Freundlich, and Temkin equilibrium models as indicated in Figure 10. Comparing the correlation coefficient of the three studied models at Table 1, it was demonstrated that Langmuir and Temkin models are the most fitted models for description the adsorption processes of diazinon onto the synthesized MIP-202/CA beads. In addition, the separation factor value (RL) in the range 0 to 1 illustrates the favorable adsorption processes of diazinon via Langmuir model [42]. However, the recorded Freundlich adsorption intensity value (nF) is 0.357, which is less than the unity, proving that the adsorption process of diazinon onto MIP-202/CA composite beads is unfavorable. On the other hand, the high value of Temkin correlation coefficient demonstrates that the equilibrium data of diazinon adsorption onto the synthesized composite bio-beads are fitted with Temkin isothermal model. Consequently, the Langmuir and Temkin models are the best favorable models for representing the monolayer chemical adsorption of diazinon on the fabricated MIP-202/CA composite beads.  To examine the diazinon adsorption mechanism onto the synthesized MIP-202/CA composite beads from waste solutions, the presented models of pseudo-first order, pseudosecond order, Elovich, and intraparticle diffusion kinetic models were achieved at Figure 11. Table 2 illustrated the comparable investigation of the R 2 values for the linear plotting of the studied kinetic models for diazinon adsorption onto the synthesized MIP-202/CA beads from waste solutions. It is clear that the linearity of plotting t/q t versus time offers a high R 2 for diazinon decontamination from wastewater indicates that the diazinon adsorption processes onto the fabricated MIP-202/CA beads agreed with the pseudo-second order kinetic model. Furthermore, the theoretical and experimental values of diazinon adsorption capacities onto the bio-beads are very close to each other. On the other hand, the correlation coefficient of Elovich equation recorded a high value of 0.921, which proposes that the diazinon adsorption process may be well explained using Elovich model. These data confirm that the studied diazinon removal process onto the fabricated MIP-202/CA beads is mainly controlled by chemisorption process [43].

Langmuir Parameters
Freundlich Parameters Temkin Parameters To examine the diazinon adsorption mechanism onto the synthesized MIP-202/CA composite beads from waste solutions, the presented models of pseudo-first order, pseudo-second order, Elovich, and intraparticle diffusion kinetic models were achieved at Figure 11. Table 2 illustrated the comparable investigation of the R 2 values for the linear plotting of the studied kinetic models for diazinon adsorption onto the synthesized MIP-202/CA beads from waste solutions. It is clear that the linearity of plotting t/qt versus time offers a high R 2 for diazinon decontamination from wastewater indicates that the diazinon adsorption processes onto the fabricated MIP-202/CA beads agreed with the pseudosecond order kinetic model. Furthermore, the theoretical and experimental values of diazinon adsorption capacities onto the bio-beads are very close to each other. On the other hand, the correlation coefficient of Elovich equation recorded a high value of 0.921, which proposes that the diazinon adsorption process may be well explained using Elovich model. These data confirm that the studied diazinon removal process onto the fabricated MIP-202/CA beads is mainly controlled by chemisorption process [43].

Regeneration Studies of the Synthesized MIP-202/CA Beads
The study of regeneration the adsorbent material is one of the most important factors because it effects the total cost of the real applications [35]. Consequently, in order to investigate the regeneration process of the fabricated MIP-202/CA beads, it was reused five times for the diazinon adsorption in the batch experiments. The adsorption-desorption data confirm the ability of MIP-202/CA composite beads to be reused after five times, where the adsorption performance decreased to 54.12% as shown in Figure 12. This excellent adsorption behavior of MIP-202/CA composite beads may be due to the cooperative influence of MIP-202, chitosan, and alginate. In addition, the existence of excess hydroxide and amine groups on the surface of the beads leads to robust attraction between the fabricated MIP-202/CA composite beads and diazinon ions.

Regeneration Studies of the Synthesized MIP-202/CA Beads
The study of regeneration the adsorbent material is one of the most important factors because it effects the total cost of the real applications [35]. Consequently, in order to investigate the regeneration process of the fabricated MIP-202/CA beads, it was reused five times for the diazinon adsorption in the batch experiments. The adsorptiondesorption data confirm the ability of MIP-202/CA composite beads to be reused after five times, where the adsorption performance decreased to 54.12% as shown in Figure 12. This excellent adsorption behavior of MIP-202/CA composite beads may be due to the cooperative influence of MIP-202, chitosan, and alginate. In addition, the existence of excess hydroxide and amine groups on the surface of the beads leads to robust attraction between the fabricated MIP-202/CA composite beads and diazinon ions.

Comparison of Adsorption Capacity for MIP-202/CA Composite Beads with Other Adsorbent Materials
In this section, the capacity of mono-layer adsorption (qm) of diazinon onto the synthesized MIP-202/CA composite beads were compared with the diazinon adsorption

Comparison of Adsorption Capacity for MIP-202/CA Composite Beads with Other Adsorbent Materials
In this section, the capacity of mono-layer adsorption (q m ) of diazinon onto the synthesized MIP-202/CA composite beads were compared with the diazinon adsorption capacities of different adsorbent materials as listed in Table 3. It was demonstrated from this table that the synthesized bio-beads have appropriate and promising efficiency for diazinon adsorption from waste solutions compared with the other reported adsorbent materials in the literature.

Conclusions
In summary, we report for the first time the efficiency of a bio-based zirconium MOF named MIP-202 for the removal of diazinon from polluted water. Since the powder form of MOFs is not applicable in most industrial applications, an eco-friendly and scalable approach for fabrication of bio based composite beads from MIP-202 powder with chitosan and alginate biopolymers named MIP-202/CA beads was developed. The resulting, highly robust, and environmentally friendly MIP-202/CA composite beads demonstrated highly efficient removal of diazinon from polluted water. The maximum adsorption capacity was determined to be 17.77 mg/g and the adsorption behavior of diazinon was fitted with Langmuir model that indicated the monolayer adsorption onto the fabricated MIP-202/CA beads. The eco-friendliness, ease of synthesis, diazinon facile adsorption, and reusability of MIP-202/CA beads make this material a promising candidate to eliminate organophosphate from waste aqueous solutions. Moreover, we believe that our generalizable and scalable approach for integrating bio-MOFs onto bio-based polymers in form of processable