Removal of Cr(VI) from aqueous solution using amino‐modified Fe3O4–SiO2–chitosan magnetic microspheres with high acid resistance and adsorption capacity

A novel, bioadsorbent material of polyethylenimine‐modified magnetic chitosan microspheres enwrapping magnetic silica nanoparticles (Fe₃O₄–SiO₂–CTS‐PEI) was prepared under relatively mild conditions. The characterization results indicated that the adsorbent exhibited high acid resistance and magnetic responsiveness. The Fe₃O₄ loss of the adsorbent was measured as 0.09% after immersion in pH 2.0 water for 24 h, and the saturated magnetization was 11.7 emu/g. The introduction of PEI obviously improved the adsorption capacity of Cr(VI) onto the adsorbent by approximately 2.5 times. The adsorption isotherms and kinetics preferably fit the Langmuir model and the pseudo‐second‐order model. The maximum adsorption capacity was determined as 236.4 mg/g at 25°C, which was much improved compared to other magnetic chitosan materials, and the equilibrium was reached within 60 to 120 min. The obtained thermodynamic parameters revealed the spontaneous and endothermic nature of the adsorption process. Furthermore, the Cr(VI)‐adsorbed adsorbent could be effectively regenerated using a 0.1 mol/L NaOH solution, and the adsorbent showed a good reusability. Due to the properties of good acid resistance, strong magnetic responsiveness, high adsorption capacity, and relatively rapid adsorption rate, the Fe₃O₄–SiO₂–CTS‐PEI microspheres have a potential use in Cr(VI) removal from acidic wastewater. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43078.     

Single step modification of micrometer-sized polystyrene particles by electromagnetic polyaniline and sorption of chromium(VI) metal ions from water

This article describes a single-step reproducible approach for the surface modification of micrometer-sized polystyrene (PS) core particles to prepare electromagnetic PS/polyaniline–Fe₃O₄ (PS/PANi–Fe₃O₄) composite particles. The electromagnetic PANi–Fe₃O₄ shell was formed by simultaneous seeded chemical oxidative polymerization of aniline and precipitation of Fe₃O₄ nanoparticles. The weight ratio of PS to aniline was optimized to produce core–shell structure. PS/PANi–Fe₃O₄ composite particles were used as adsorbent for the removal of Cr(VI) via anion-exchange mechanism. The composite particles possessed enough magnetic property for magnetic separation. The adsorption was highly pH dependent. Adsorption efficiency reached 100% at pH 2 in 120 min when 0.05 g of composite particles was mixed with 30 mL 5 mg L⁻¹ Cr(VI) solution. The adsorption isotherm fitted best with Freundlich model and maximum adsorption capacity approached 20.289 mg g⁻¹ at 323 K. The prepared composite was found to be an useful adsorbent for the removal of soluble Cr(VI) ions. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47524.     

Synthesis,characterization of Fe3O4@glycine doped polypyrrole magnetic nanocomposites and their potential performance to remove toxic Cr(VI)

Fe₃O₄ coated glycine doped polypyrrole magnetic nanocomposite (Fe₃O₄@gly-PPy NC) was prepared via coating of suspended Fe₃O₄ nanoparticles with gly-PPy. FE-SEM and HR-TEM images indicated that Fe₃O₄ nanoparticles were encapsulated by precipitating gly-PPy moieties. Chromium(VI) adsorption followed a Langmuir isotherm with maximum capacity of 238–303 mg/g for a temperature range of 25–45 °C at pH 2. The adsorption process was governed by the ionic interaction and the reduction of Cr(VI) to Cr(III) by the PPy moiety. Results showed that NCs are effective adsorbents for the removal of Cr(VI) from wastewater and can be separated by external magnetic field from the reactor.     

Removal of Cr(VI) from aqueous solution using magnetite/non-oxidative graphene composites: Synergetic effect of Cr(VI) on dyes removal

Non-oxidative graphene (nOG) synthesized from natural graphite powder was modified with magnetite (Fe₃O₄) for removal of Cr(VI) and dyes in aqueous solution. The adsorption behavior of Cr(VI) on Fe₃O₄/nOG (M-nOG) was systematically investigated, and the simultaneous adsorption of Cr(VI) and dyes such as methylene blue (MB) and rhodamine B (RhB) was evaluated. Adsorption kinetic and isotherm of Cr(VI) were fitted well with pseudo-second-order model and Sips model, respectively. For the binary system, Cr(VI) removal was not affected with increasing the dye concentration, whereas the adsorption capacity of both MB and RhB was enhanced with increasing the concentrations of Cr(VI).     

Chemically Modified CaO/Fe3O4 Nanocomposite by Sodium Dodecyl Sulfate for Cr(III) Removal from Water

A CaO/Fe₃O₄ nanocomposite was modified by sodium dodecyl sulfate (SDS) and used for Cr(III) removal from aqueous solution. The physical and surface characteristics of the adsorbent were studied by different analysis techniques. The effects of key parameters such as pH, contact time, temperature, initial concentration of Cr(III) ions, and adsorbent dose were investigated at a fixed mixing rate. Parameters were optimized to attain the best possible removal efficiency of Cr(III) ions. The maximum adsorption capacities obtained from the Langmuir model were determined. The results of equilibrium and kinetic studies indicate that the adsorption process follows the Langmuir isotherm model and the pseudo‐second‐order kinetic model. The thermodynamic study demonstrated that the adsorption process was suitable, spontaneous, and exothermic.     

Magnetite/graphene/polyaniline composite for removal of aqueous hexavalent chromium

Here, we report the synthesis of Fe₃O₄/G/PANI composite containing magnetite nanoparticles (Fe₃O₄), graphene sheets (G), and polyaniline (PANI) via chemical route for removal of toxic Cr (VI) from water. TEM image shows the formation of uniformly distributed magnetite nanoparticles on graphene/PANI composite. HRTEM images shows the formation of crystalline magnetite nanoparticles showing lattice fringes with inter‐planner distance 0.21 nm. The magnetic measurement shows magnetization 22 emu/g and ferromagnetic property of the adsorbent. The equilibrium adsorptions were well‐described by the Langmuir isotherm model and shows maximum adsorption capacity 153.54 mg/g at pH 6.5 and temperature 30 °C. The kinetics data well fitted by pseudo‐second‐order model and around 86% Cr (VI) removal completed within 20 min. The Cr (VI) removal capacitive decreases with increase in pH and ionic strength. The adsorbent shows leaching of iron nanoparticles at pH 1 whereas stable in solution having pH 2 and more. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44002.     

Facile preparation of magnetic chitosan modified with thiosemicarbazide for adsorption of copper ions from aqueous solution

In this study, magnetic chitosan modified with thiosemicarbazide (TSC‐Fe₃O₄/CTS) was facilely synthesized with glutaraldehyde as the crosslinker, and its application for removal of Cu(II) ions was investigated. The as‐prepared TSC‐Fe₃O₄/CTS was characterized by Fourier transform infrared spectroscopy (FTIR), X‐ray powder diffraction (XRD), and scanning electron microscopy (SEM). The results showed that TSC‐Fe₃O₄/CTS has high adsorption capacity and selectivity towards Cu(II) ions. Adsorption experiments were carried out with different parameters such as pH, solution temperature, contact time and initial concentration of Cu(II) ions. The adsorption process was better described by the pseudo‐second‐order model. The sorption equilibrium data was fitted well with the Langmuir isotherm model and the maximum adsorption capacity toward Cu(II) ions was 256.62 mg/g. The thermodynamic parameters indicated that the adsorption process of Cu(II) ions was exothermic spontaneous reaction. Moreover, this adsorbent showed excellent reusability and the adsorption property remained stable after five cycles. This adsorbent is believed to be one of the promising and favorable adsorbent for the removal of Cu(II) ions from aqueous solution. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44528.     

Removal of chromium(VI) from aqueous solutions using polypyrrole-based magnetic composites

PPy/Fe₃O₄/AgCl composites were prepared via in situ polymerization for the removal of highly toxic Cr(VI). The structure and morphology of the prepared composites were characterized by the XRD, SEM, TEM, and VSM examinations. Up to 100 % removal was found with 1000 mg/L Cr(VI) aqueous solution at pH 2.0. The process of Cr(VI) ions’ adsorption was easy to reach equilibrium at higher temperatures. Adsorption results showed that Cr(VI) removal efficiency by the composites decreased with an increase in pH. Adsorption kinetics was described by the pseudo-second-order rate model. Isotherm data fitted well to the Langmuir isotherm model. Desorption experiment showed that the regenerated adsorption of PPy/Fe₃O₄/AgCl can be reused successfully for three times successive adsorption–desorption cycles without appreciable loss of its original capacity.     

Synthesis of Fe2O3-coated and HCl-treated bauxite ore waste for the adsorption of arsenic (III) from aqueous solution: Isotherm and kinetic models

The present work has focused on the removal of arsenic (III) using two effective adsorbents such as red mud treated with HCl and coated with Fe₂O₃. Adsorption of As (III) was performed by the function of pH, adsorbent dose, contact time, initial ion concentration, and the appropriate conditions for adsorption were determined. The characterization studies of the adsorbent were analyzed using X-ray diffraction, X-ray fluorescence, Brauner–Emmett–Teller, scanning electron microscope, and FTIR spectroscopy. The result of the studies shows that the adsorbent is suitable for the effective removal of As (III) ions. Batch adsorption process showed that the maximum adsorption occurred at Fe₂O₃-coated red mud. The equilibrium data were well fitted to the nonlinear Langmuir isotherm model and the maximum adsorption capacity (q_m) of Fe₂O₃-coated red mud was found to be 21.85?mg?g^?1 which indicates that Fe₂O₃-coated red mud had more adsorption capacity. In the Freundlich isotherm, the experimentally obtained n value of Fe₂O₃-coated red mud was 2.393 which indicates the favorable adsorption of As (III) on the adsorbent. Dubinin–Radushkevich isotherm confirms that the adsorption process is physical in nature. Furthermore, the adsorption kinetic studies followed the pseudo-first-order model. All the results concluded that Fe₂O₃-coated red mud can be considered as a cost-effective and potential adsorbent for As (III) removal.     

Polypyrrole/NiFe2O4 composites with improved hexavalent chromium removal from aqueous solution

Polypyrrole/NiFe₂O₄ (PPy/NiFe₂O₄) composites were prepared by ultrasonic oxidative polymerization in the presence of NiFe₂O₄ nanoparticles (NPs). The nanostructure of PPy/NiFe₂O₄ was confirmed by the X‐ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), and vibrating sample magnetometer (VSM) examinations. The adsorption of Cr(VI) onto the PPy/NiFe₂O₄ composite was lowly pH dependent and the adsorption kinetics followed the Pseudo‐second‐order model. The Langmuir isothermal model well described the adsorption isotherm data and the maximum adsorption capacity increased with the increase of temperature. The maximum adsorption capacity of the PPy/NiFe₂O₄ for Cr(VI) ions was up to 50 mg/g at pH 2.0. The excellent adsorption characteristic of PPy/NiFe₂O₄ composite will render it a highly efficient and economically viable adsorbent for Cr(VI) ions removal. POLYM. COMPOS., 38:2779–2787, 2017. © 2015 Society of Plastics Engineers     

Enhanced catalytic oxidation via nano Cu0.5Mg0.5Fe2O4 embedded in CNTs for adsorption–reduction of hexavalent chromium

A catalyst consisting of Cu_0.5Mg_0.5Fe₂O₄ (CMF) supported on carbon nanotubes (CNTs) which exhibits great potential as an adsorbent for treating Cr(VI)-contaminated wastewater has been successfully prepared. The ferrite possesses excellent magnetic properties, while CNTs have the advantage of a large surface area. This composite material not only prevents the aggregation of magnetic materials and enhances the exposure of active sites but also effectively solves the recycling problem of CNTs. Our results show that the adsorption capacity of Cu_0.5Mg_0.5Fe₂O₄–carbon nanotubes (CMF-CNTs) for Cr(VI) wastewater (45.60 mg/g) is 1.49 times higher than that of Cu_0.5Mg_0.5Fe₂O₄ (30.48 mg/g). Compared to a single catalyst, CMF-CNTs not only improve the dispersibility of magnetic materials but also exhibit synergistic effects between the composite materials, enhancing the chemical adsorption capacity. After five consecutive adsorption and desorption experiments, the adsorption capacity of CMF-CNTs remains at 88% of its initial value. Furthermore, the study of the catalyst before and after adsorption by XPS reveals that the valence state transition of Fe³⁺/Fe²⁺ and Cu²⁺/Cu⁺ plays a crucial role in the adsorption process. The results of this study demonstrate the potential of using waste materials for effective wastewater treatment and provide insights into the development of new adsorbents for pollutant removal.     

One-step solvothermal synthesis of Fe3O4@Carbon composites and their application in removing of Cr (VI) and Congo red

Fe₃O₄ @C nano-adsorption was prepared by a simple one-step solvothermal synthesis method using Fe (NO₃)₃ 、cyclodextrin as raw materials, meanwhile urea as an alkali source. The obtained samples were characterized by X-ray diffraction, Raman spectroscopy, transmission electron microscopy, scanning electron microscopy, and Brunauer-Emmett-Teller. The adsorption behavior of the Fe₃O₄@C toward Cr (VI) and Congo red was also studied. The core-shell structure Fe₃O₄@C exhibited large specific surface area of 112.91?m² g^?1. The prepared Fe₃O₄@C samples demonstrated typical ferromagnetic behavior and high removal capacity in removing the toxic Cr (VI) ions and organic pollutant CR from wastewater, together with facile magnetic separability and good recyclability. Equilibrium adsorption performance was conducted by using the Langmuir and Freundlich model and Freundlich model could simulate the adsorption process of Congo red and Cr (VI) better. The maximum adsorption capacity of Cr (VI) and Congo red was 33.35?mg?g^?1 and 262.72?mg?g^?1 by calculation.     

Preparation and characterization of higher degree‐deacetylated chitosan‐coated magnetic adsorbent for the removal of chromium(VI) from its aqueous mixture

Chitosan (90% deacetylated) coated magnetic adsorbent prepared by coprecipitation method to remove Cr(VI) from its aqueous solution. The experimental studies depicts that the predominant option for removal of Chromium by adsorption from its aqueous phase using Magnetic‐Chitosan (MC). The subsequent physical, chemical, and magnetic properties of MC were characterized by X‐ray powder diffraction, scanning electron microscopy, Fourier transform infrared spectrometer, vibrating sample magnetometer. The influence of batch process parameters such as contact time, initial concentration, pH, and coexisting anions were investigated. The Box‐Behnken experimental design in response surface methodology was performed to design the experiment optimal operating conditions. The maximum percentage reduction of Cr(VI) is 96.3 that was obtained by magnetic chitosan with the optimal operating conditions of 149.53 mg/L at pH of 5.32 at the contact time of 80 min and at the temperature of 303 K. The average diameter of the magnetic chitosan was calculated from X‐ray diffractometer analysis as 24.5 nm. The equilibrium adsorption isotherm models such as Langmuir and Freundlich and the adsorption kinetics such as pseudo first order, pseudo second order and intra‐particle diffusion kinetic model were analyzed. The experimental data's suited for the best fit with the Langmuir isotherm model and pseudo first order kinetic model. It also revealed that Cr(VI) adsorption on MC is intrinsically exothermic and spontaneous. The magnetic chitosan was also used to investigate for the removal of Cr(VI) from the real water sources such as surface, underground, and tannery wastewater. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45878.     

Fabrication of a copolymer flocculant and application for Cr(VI) removal

A copolymer flocculant (CATCS) derived from starch and chitosan was fabricated and used as eco‐friendly adsorbent for removal of Cr(VI) from aqueous solution. The CATCS flocculant was characterized by scanning electron microscope, thermogravimetic analysis, and Fourier transform infrared spectroscopy. The effects of CATCS dosage, initial Cr(VI) concentration, pH, and reaction time on removal of Cr(VI) were discussed. The results showed CATCS removed Cr(VI) effectively and the adsorption isotherm agreed well with the Freundlich isotherm and R–P isotherm models. The enthalpy change (ΔH) of the process was 16.75 kJ/mol suggesting the existence of chemisorption and the reaction was endothermic. Moreover, the negative free energy change (ΔG) indicated the adsorption process was feasible and spontaneous. The positive entropy change (ΔS) showed there was an increase of disorder in the system during the adsorption process. The adsorption kinetics results showed that the adsorption could be described by the pseudo‐second‐order kinetics mechanism. The activation energy (E_a) of the adsorption reaction was 29.16 kJ/mol. POLYM. ENG. SCI., 56:1213–1220, 2016. © 2016 Society of Plastics Engineers     

Comparison of Cr(VI) Adsorption Using Synthetic Schwertmannite Obtained by Fe3+ Hydrolysis and Fe2+ Oxidation: Kinetics,Isotherms and Adsorption Mechanism

Good sorption properties and simple synthesis route make schwertmannite an increasingly popular adsorbent. In this work, the adsorption properties of synthetic schwertmannite towards Cr(VI) were investigated. This study aimed to compare the properties and sorption performance of adsorbents obtained by two methods: Fe³⁺ hydrolysis (SCH_A) and Fe²⁺ oxidation (SCH_B). To characterise the sorbents before and after Cr(VI) adsorption, specific surface area, particle size distribution, density, and zeta potential were determined. Additionally, optical micrographs, SEM, and FTIR analyses were performed. Adsorption experiments were performed in varying process conditions: pH, adsorbent dosage, contact time, and initial concentration. Adsorption isotherms were fitted by Freundlich, Langmuir, and Temkin models. Pseudo-first-order, pseudo-second-order, intraparticle diffusion, and liquid film diffusion models were used to fit the kinetics data. Linear regression was used to estimate the parameters of isotherm and kinetic models. The maximum adsorption capacity resulting from the fitted Langmuir isotherm is 42.97 and 17.54 mg·g⁻¹ for SCH_A and SCH_B. Results show that the adsorption kinetics follows the pseudo-second-order kinetic model. Both iron-based adsorbents are suitable for removing Cr(VI) ions from aqueous solutions. Characterisation of the adsorbents after adsorption suggests that Cr(VI) adsorption can be mainly attributed to ion exchange with SO₄²⁻ groups.     

Fe2+-modified Vermiculite for the Removal of Chromium (VI) from Aqueous Solution

A novel adsorbent: Fe²⁺-modified vermiculite was prepared in a two-step reaction. Adsorption experiments were carried out as a function of pH, contact time, and concentration of Cr(VI). It was found that Fe²⁺-modified vermiculite was particularly effective for the removal of Cr(VI) at pH 1.0. The adsorption of Cr(VI) reached equilibrium within 60 min, and the pseudo-second-order kinetic model best described the adsorption kinetics. The adsorption data follow the Langmuir model more than the Freundlich model. At pH 1.0, the maximum Cr(VI) sorption capacity (Q _max ) was 87.72 mg · g^?1. Desorption of Cr(VI) from Fe²⁺-modified vermiculite using NaOH treatment exhibited a higher desorption efficiency by more than 80%. The sorption mechanisms including electrostatic interaction and reduction were involved in the Cr (VI) removal. The results showed that Fe²⁺-modified vermiculite can be used as a new adsorbent for Cr(VI) removal which has a higher adsorption capacity and a faster adsorption rate.     

Hexavalent chromium adsorption on superparamagnetic multi-wall carbon nanotubes and activated carbon composites

Hexavalent chromium (Cr(VI)) adsorption from aqueous solutions on magnetically modified multi-wall carbon nanotubes (M-MWCNT) and activated carbon (M-AC) was investigated. M-MWCNT and M-AC were prepared by co-precipitation method with Fe²⁺:Fe³⁺ salts as precursors. The magnetic adsorbents were characterized by X-ray diffraction (XRD), thermogravimetric analysis (TGA) and scanning electron microscope (SEM). The effects of amount of adsorbents, contact time, initial pH, temperature and the initial concentration of Cr(VI) solution were determined. The adsorption equilibrium, kinetics, thermodynamics and desorption of Cr(VI) were investigated. Equilibrium data fitted well with the Langmuir isotherm for both of the adsorbents. The theoretical adsorption capacities are 14.28 mg/g of M-MWCNT and 2.84 mg/g of M-AC. Cr(VI) adsorption kinetics was modeled with pseudo-second order model, intra-particle diffusion model and Bangham model. Thermodynamic parameters were calculated and ΔG°, ΔH° and ΔS° indicate that the adsorption of Cr(VI) onto M-MWCNT and M-AC was exothermic and spontaneous in nature. Results revealed that M-MWCNT is an easily separated effective adsorbent for Cr(VI) adsorption from aqueous solution.     

Adsorption of Cr(VI) on Cross‐Linked Chitosan Beads

Abstract

A possibility of Cr(VI) removal by the adsorption method is discussed in the paper. An adsorbent were hydrogel chitosan beads are produced by the phase inversion method (by changing pH). The possibility of removing Cr(VI) ions by both pure chitosan hydrogel and its chelate compounds (chitosan cross‐linked with Cu(II) and Ag(I) ions) was investigated. The adsorption proceeded from the solutions of potassium dichromate and ammonium dichromate (NH₄)₂Cr₂O₇ and K₂Cr₂O₇. The process rates and adsorption isotherms were determined and described by relevant equations. The process rate was described by the pseudo‐ and second‐order equations, and adsorption equilibria by the Langmuir equations. A slight advantageous change in adsorption properties of chitosan beads was revealed after cross‐linking (for chromium concentration up to 10 g/dm³). A maximum adsorption was 1.1 g_Cr/g chitosan. Results of the studies show that chitosan hydrogel proves useful in the removal of Cr(VI) ions, additionally, cross‐linking with Cu(II) and Ag(I) ions has an advantageous effect in the case of low‐concentrated solutions.     

In situ preparation of magnetic Fe3O4.Cu2O.Fe3O4/cryogel nanocomposite powder via a reduction–coprecipitation method as adsorbent for methylene blue water pollutant

Magnetic nanocomposites have attracted great attention as adsorbents for the removal of water pollutants, which respond to an external magnet that is used to remove both pollutants and composite nanomaterial traces from water. They are environmentally friendly and effective adsorbents for water treatment. In this respect, a simple in situ preparation method was used to prepare cryogel powder composite based on Fe₃O₄.Cu₂O.Fe₃O₄ nanomaterials. The ionic cryogel based on 2‐acrylamido‐2‐methylpropane sulfonate sodium salt and styrene sulfonate sodium salt was prepared by crosslinking polymerization at low temperature. The new magnetic nanoparticles based on Fe₃O₄.Cu₂O.Fe₃O₄ were successfully prepared inside the cryogel networks by a simple reduction–coprecipitation method based on reaction of Fe³⁺ with sodium sulfite and Cu²⁺ in the presence of hydroxylamine and ammonia solution. The thermal stability, accurate Fe₃O₄.Cu₂O.Fe₃O₄ content, magnetic properties, crystal lattice structure, particle sizes and morphology of the prepared cryogel composite were evaluated. The optimum conditions such as pH, contact time, adsorbate concentrations, adsorption equilibrium and adsorption kinetics were investigated to determine the efficiency of the prepared composite as an adsorbent to remove toxic methylene blue (MB) pollutant from aqueous solution. The data for MB adsorption confirmed the high ability of the prepared composite to remove more than 4.696 mmol L^?1 of MB from water during 6 min. The regeneration and reuse experiments showed excellent data for the synthesized new dye as an effective adsorbent for water treatment. © 2018 Society of Chemical Industry     

Polydopamine interface encapsulating graphene and immobilizing ultra-small,active Fe3O4 nanoparticles for organic dye adsorption

In this study, a combined process of bio-inspired modification and magnetic treatment is presented for the preparation of a polydopamine (Pdop)-modified graphene (Pdop-G)-based adsorbent which incorporates ultra-small, active Fe₃O₄ nanoparticles (with an average size of 6.5 nm). Not only can the nanoparticles impart superparamagnetism to the modified graphene adsorbent but also enhance the adsorption performance. The ultra-small size of Fe₃O₄ nanoparticles allows the exposure of a high proportion of low-coordinated sites such as corners and edges. Additional active sites can thus be provided to bind methylene blue molecules, in addition to the active Pdop-G surface with catechol and amine groups which induce hydrogen bonding, electrostatic attraction, and π-π stacking interactions. The Pdop interface wraps graphene and immobilizes Fe₃O₄, endowing the magnetic Pdop-G (MPG) with high adsorption capacity, easy recyclability, and excellent reusability for the organic pollutant removal. In stark contrast, the counterpart without the interfacial Pdop layer suffers from severe Fe₃O₄ aggregation, causing its adsorption performance inferior to that of MPG. The MPG-based adsorption obeys the pseudo-second-order kinetics, and the intraparticle diffusion model also indicates the complex adsorption pathway, including the external and intraparticle mass transfer. The Langmuir isotherm can better fit the experimental data than the Freundlich isotherm, with the theoretical maximum adsorption capacities estimated to be 131.6, 140.3, and 152.0 mg/g at 30, 40, and 50 °C, respectively. The adsorption is endothermic and spontaneous, along with an increase in the randomness at the solid-solution interface. The separation factor (R_L) reveals the favorable adsorption process with MPG. The superparamagnetism imparted via the Fe₃O₄ composition makes MPG easily recyclable. Furthermore, the removal rate can be maintained at about 90% after 5 runs of repeated usage of MPG. This study opens up a new avenue to the magnetization of adsorbents for enhancing adsorption performance in addition to imparting magnetism.