Functionalized magnetic biopolymeric graphene oxide with outstanding performance in water purification

Graphene oxide (GO) is an attractive material for water treatment, although its high surface energy restricts its practical application. To overcome this challenge, we have developed a well-dispersed and interconnected, functionalized biopolymeric GO with magnetic activity, namely, cl–CS–p(MA)/Fe3O4NPs. This three-dimensional, sponge-like nanostructured material is composed of graphene oxide nanosheets dispersed in functionalized chitosan/poly(methacrylic acid) and is cross-linked with in situ-developed Fe3O4 nanoparticles. Methacrylic acid (MA)-functionalized chitosan (CS) cross-linked with N,N-methylenebis(acrylamide) (MBA), designated as cl–CS–p(MA), facilitates the stable dispersion of GO nanosheets, providing a proper solid matrix for the generation of well-dispersed in situ Fe3O4NPs. The methodology allows for the generation of numerous binding sites with an interconnected morphology, facilitating the rapid uptake of a cationic dye in significant quantity, e.g., methylene blue (MB), which is used as a model water pollutant. In this work, the structural architecture of cl–CS–p(MA)/Fe3O4NPs was characterized with multiple approaches, and the adsorption mechanism was revealed to be an electrostatic interaction. The synthesized nanocomposite showed significant recyclability and structural stability. Adsorption equilibrium was achieved within 20 min, and the maximum adsorption capacity was 2478 mg/g for MB, surpassing the values reported for any other adsorbents to date. Nanostructured biopolymer proposes an efficient environmental clean-up. The deliberate introduction of graphene oxide and in situ generated magnetic iron oxide nanoparticles into the functionalized biopolymer helps to form a structurally stable magnetic nanostructured material. Amit Kumar Sarkar and Yeoung-Sang Yun and their colleagues from Chonbuk National University, South Korea have shown that the material adsorbs methylene blue with a high adsorption capacity (2,478 milligram per gram) at a fast removal rate. The synergistic development of the material through functionalization and cross-linking leads to the generation of well-dispersed high-density active adsorption sites with enormous microchannels in the nanocomposite, which are responsible for the efficient pollutant uptake. The researchers pointed out that graphene oxide plays a vital role in the structural stability of the material and the generation of well-dispersed active binding sites is more important than the porosity or surface area of the material. A sponge-like material that can purify water has been developed by scientists in South Korea. Making water safe requires technologies that can remove almost any pollutant. This need is likely to increase as the world’s population grows and access to fresh water becomes scarcer. Nanomaterials offer one possible solution. Graphene-oxide membranes, for example, can absorb toxic organic solvents and other hazardous chemicals but further improvements in adsorption capacity and material recyclability are needed before their use becomes practically viable. Amit Kumar Sarkar from Chonbuk National University, Jeonbuk and colleagues synthesized a three-dimensional sponge-like nanomaterial by using iron oxide nanoparticles to link two-dimensional graphene oxide nanosheets dispersed in the functionalized chitosan. The team demonstrated that their material could rapidly adsorb methylene blue, a model water pollutant, more effectively than any other material reported to date.


Introduction
The rapid development of nanotechnology and the design of nanostructured materials have led to noteworthy breakthroughs in various fields and applications 1,2 . In macroscopic structures, the effective growth of nanoparticles (NPs) introduces synergy in novel assemblies of nanostructured composites, which can be used to translate unique properties from individual NPs to nanostructured materials 3 . Such nanostructured materials are enriched with tunable surface functionalities, structural stability, and high adsorption capacities 4 . By taking advantage of these features, the performance of wastewater remediation technology could be significantly enhanced by using nanostructured materials. The efficient treatment of wastewater has the potential to minimize the scarcity of clean water in domestic, agricultural, and industrial perspectives.
Among the various types of water pollutants, colored organic dyes pose significant threats to human health and the environment and are aesthetically objectionable 5 . The discharge of untreated dye wastewater, even at a very low concentration (<1 mg/L), is unacceptable. Among the various technologies that have been deployed for dye removal, adsorption is considered to be one of the easiest, most effective, and inexpensive methods 6 . An efficient adsorbent must have sufficient chemical stability, have enough active adsorption sites for effective contact with adsorbates, and be recyclable to enable easy separation and regeneration of the adsorbent under experimental conditions. The conventionally activated carbons and natural zeolites have been used as adsorbent materials in past studies 7,8 . However, such materials show low surface functionalities, limited adsorption capacities, and slow kinetics. Therefore, the fabrication of a single adsorbent material with a high adsorption capacity, rapid kinetics, structural stability, and recyclability remains a strategic challenge.
Nanostructured composite materials have attracted significant attention as new-generation adsorbents for dye removal. Examples include clays, exfoliated titanate layers, mesoporous carbons, carbon nanofibers, and polyanilines, all of which have been used as the main constituent of nanocomposite/composite building blocks [9][10][11][12][13][14] . Among these materials, graphene oxide (GO), a two-dimensional (2D) carbon nanomaterial, offers attractive and unique physicochemical properties 15 and is considered an excellent adsorbent 16 . However, the use of GO as an adsorbent has been restricted because of the high surface energy of GO sheets, which can lead to aggregation through van der Waals interactions, in addition to the ultrahigh centrifugation needed to collect GO after pollutant removal 17 . Consequently, modified GOs have been used in aqueous media to increase the separation efficiency of GO-based adsorbents; examples include threedimensional GO sponges, a magnetic GO/poly(vinyl alcohol) composite gel, and poly(acrylic acid)-modified magnetic GO with reported MB dye adsorption capacities of 467, 270.94, and 290.7 mg/g, respectively [17][18][19] . Although the reported GO-based adsorbents may eventually overcome the separation problem, they lack the significant uptake capacity necessary for handling aqueous pollutants. The subsequent assembly of GO into macroscopic structures yielded a better adsorption performance; for example, nanoporous GO sponges and GO beads were effective for the removal of toxic organic solvents and hazardous chemicals from water 20,21 . Polymeric brushes of poly(acrylamide) grafted onto reduced GO sheets behaved as an effective adsorbent for MB (1530 mg/g) and Pb 2+ (1000 mg/g) 22 . Recently, GO/chitosan (CS) microspheres were developed for the rapid removal of MB (584.6 mg/g) and Cr(VI) (292.8 mg/g) 23 .
Numerous efforts have been made to develop functional and recyclable GO-based adsorbents. However, an adsorbent that meets the required specifications, such as rapid achievement of equilibrium and excellent adsorption capacity, separation ability, and recyclability, has not yet been developed. Bearing in mind the aforementioned challenges for a high-performance advanced adsorbent, we developed a novel synthesis strategy to obtain crosslinked polymeric hybrid nanocomposites, namely, cl-CS-p(MA)/Fe 3 O 4 NPs. The nanocomposite was prepared by unstacking GO nanosheets by infiltrating with methacrylic acid (MA)-functionalized chitosan (CS) cross-linked with N,N′-methylenebis(acrylamide) (MBA), designated as cl-CS-p(MA), and cross-linking with in situ-generated Fe 3 O 4 NPs. CS, a cationic biopolymer of glucosamine and N-acetylglucosamine, shows pHtriggered self-assembly responsiveness 24 . Herein, the implemented approach is discussed for the first time. To understand the individual role of each component in the nanocomposite, controlled adsorption studies were carried out using cl-CS-p(MA), cl-CS-p(MA)/GO (without Fe 3 O 4 ), and cl-CS-p(MA)/Fe 3 O 4 (without GO). We are delighted to report that the synthesized cl-CS-p(MA)/ GO-Fe 3 O 4 NPs can rapidly capture the cationic MB dye and showed an outstanding MB dye adsorption capacity of 2478 mg/g, which is the highest reported value to date. The excellent adsorptive characteristics of this nanocomposite arise from the combined synergistic effect of well-dispersed active binding sites and interconnected microchannels, which facilitate rapid adsorption. More interestingly, the developed adsorbent was structurally stable over the entire pH range (pH 3-9) and can easily be separated using an external magnet and spatula.

Preparation of cross-linked chitosan [cl-CS-p(MA)]
The cross-linked chitosan was synthesized using a free radical polymerization approach. Chitosan (0.5 g) was dissolved in 80 mL of 0.1 M acetic acid solution in a threenecked round-bottom (RB) flask. The RB flask was positioned in an electrically operated oil bath, and a thermometer was used to maintain the temperature at 65°C throughout the reaction. Then, the whole system was placed over a magnetic stirrer for continuous stirring at 350 rpm. After maintaining an inert atmosphere of N 2 in the RB flask, 3.699 × 10 -5 mol of KPS was added. Successively, after 10 min of intervals, 0.1178 mol of MA followed by 3.243 × 10 -5 mol of MBA were carefully added into the reaction system. The cross-linking copolymerization reaction was allowed to continue up to 3 h of reaction time, maintaining the same reaction temperature while stirring. Once the reaction mixture had turned to a thick white gel, the polymerization was terminated using an aqueous solution of saturated hydroquinone. Subsequently, the cooled white gel was washed with 400 mL of 1:1 methanol-acetone mixture to remove the unreacted monomer and homo polymer. Finally, the washed product was dried using a freeze dryer.

Synthesis of cl-CS-p(MA)/GO-Fe 3 O 4 NPs
GO was prepared using a modification of Hummer's method (experimental details in the Supporting Information) 25,26 . A gelling matrix of cl-CS-p(MA) (1 g) was prepared in 100 mL of 0.01 (N) NaOH solution at 65°C with constant stirring. Next, a fixed quantity of GO (0.06 g) in 10 mL of water was placed under sonication for 15 min. Afterward, the aqueous solution of GO was added into the gelling matrix using a dropping funnel under the presence of N 2 atmosphere at 65°C for 15 h. Next, 5 mL of each aqueous solution of 0.278 g of ferrous sulfate (FeSO 4 ) and 0.540 g of ferric chloride (FeCl 3 ) was added while maintaining the same experimental conditions, followed by the addition of 9 mL of ammonia solution. After 6 h of continuous stirring, the reaction mixture was allowed to cool and then was precipitated in acetone, resulting in a black spongy material. The material was washed with water and placed in a desiccator overnight at room temperature.

Characterizations
Fourier transform-infrared spectrometry (FT-IR) (Jasco FT/IR-4100, Japan) was performed using a scan range of 400-4000 cm -1 with pressed KBr pellets. Powder X-ray diffraction (XRD) spectra were collected with a scan range of 5-80°and scan rate of 2°/min (X'pert PRO, PANalytical, Netherlands), installed in the Center for University-Wide Research Facility (CURF), Chonbuk National University, Korea. Surface morphologies were imaged using field-emission scanning electron microscopy (FE-SEM) coupled with energy-dispersive spectroscopy (EDS) (SUPRA 40VP, Carl Zeiss, Germany) and a CS-corrected field-emission transmission electron microscope (JEOL, JEM-ARM-200F, Japan) from CURF. X-ray photoelectron spectroscopy (XPS) was carried out using K-Alpha spectrometer (ThermoFisher Scientific, UK) with monochromated Al Kα radiation (1486.6 eV) and peaks were deconvoluted/optimized using XPSPEAK 4.1 software. Raman spectroscopy was performed using a Nanofinder 30 (Tokyo Instrument, Japan), from Korea Basic Science Institute (KBSI), Jeonju center, Korea. The point of zero charge (pH pzc ) of cl-CS-p(MA)/GO-Fe 3 O 4 NPs was measured using the pH drift method 27 (the procedure is described in the Supporting Information). The specific surface area and mean pore size were measured by the Brunauer-Emmett-Teller (BET) method (BELSORPmax/MicrotracBEL Corp., Japan at 77 K). The magnetic property of the synthesized nanocomposite was recorded using a vibrating sample magnetometer (VSM, Lakeshore 7404, USA) operated at room temperature. Adsorption studies were done using UV-VIS spectrophotometer (UV-2550, Shimadzu, Japan).

Dye adsorption study
A stock solution of MB (2000 mg/L) was prepared and diluted to obtain the required experimental concentrations. The batch experiments were performed with 20 mL of known MB dye solution in the presence of 0.01 g of cl-CS-p(MA)/GO-Fe 3 O 4 NPs as the adsorbent in 50-mL Falcon tubes. The Falcon tubes were placed in an electrically operated multishaking incubator at 25°C and 120 rpm. We examined a range of MB concentrations (100 -1,700 mg/L) for isotherm study at pH 8.5 ± 0.1. All adsorption studies were performed twice. A kinetic study was performed using 100 mg/L of MB dye and cl-CS-p (MA)/GO-Fe 3 O 4 NPs at pH 8.5 ± 0.1. The experimental procedures are described in detail in the Supporting Information. The % of MB adsorption and equilibrium uptake capacity were determined using equations (1) and (2), respectively. A detailed explanation behind these calculations is given in the Supporting Information.
Equilibrium uptake capacity Effect of dye type on removal efficiency The efficiency of the cl-CS-p(MA)/GO-Fe 3 O 4 NPs in removing different types of dyes was examined with two dye mixtures: mixture I (MB + TB) and mixture II (MB + MO). Mixture I included two cationic dyes (MB and TB) at 10 mg/L each; mixture II contained cationic MB and anionic MO at 10 mg/L each. To evaluate the adsorption behaviors of the dye mixtures, 0.01 g of cl-CS-p(MA)/ GO-Fe 3 O 4 NPs was brought into contact with 20 mL of each dye mixture at pH 8.5 in a shaking incubator at 25°C and 120 rpm.

Stability study of cl-CS-p(MA)/GO-Fe 3 O 4 NPs
The stability of the adsorbents over a wide range of pH values is a critical parameter toward ensuring that the adsorbents do not disperse or solubilize upon contact with aqueous media. Thus, a fixed amount of cl-CS-p (MA)/GO-Fe 3 O 4 NPs was separately added into 20 mL of acidic (pH 3 ± 0.5), neutral (pH 7 ± 0.5), or basic (pH 9 ± 0.5) solution in 50-mL Falcon tubes. The Falcon tubes were placed in the incubator for 24 h at 25°C. During that time, the structural stability of the cl-CS-p(MA)/ GO-Fe 3 O 4 NPs was monitored.

Recyclability test
An ideal adsorbent must have regeneration properties. Thus, MB-loaded cl-CS-p(MA)/GO-Fe 3 O 4 NPs were recycled from the experimental aqueous media using an external magnet or spatula based on a desorption process.

Results and discussion
This synthesis approach relies on the functionalization of MA onto the backbone of CS in the presence of MBA as the cross-linker. Free radical sites were generated on the CS backbones using KPS as an initiator at 65°C and then were allowed to react with MA, which underwent cross-linking polymerization through chain reactions in the presence of the reactive sites of MBA to form a 3D cross-linked polymer hydrogel ( Fig. 1a; Scheme S1, Supporting Information). The resulting cl-CS-p(MA) hydrogel was used as a gelling matrix to stabilize the GO layers. Then, the synthesized cl-CS-p(MA)/GO underwent further cross-linking with in situ-developed Fe 3 O 4 NPs. The presence of GO in the nanocomposite provided the overall stability of the cross-linked 3Dnanostructured material (Fig. 1a; Scheme S1, Supporting Information). Herein, a stable dispersion of unstacked GO nanosheets was prepared in the presence of the gelling matrix of cl-CS-p(MA). Next, the stable gelling dispersion of the GO nanosheets and carboxylate side chains of cl-CS-p(MA) minimized the possibility of Fe 3 O 4 NP agglomeration; this stabilization effect was achieved through cross-linking reactions and led to the development of a sponge-like material with magnetic behavior (Fig. 1(b-e), inset images).
Several characterization techniques were utilized to confirm the development of nanocomposites through polymerization and in situ cross-linking. The XRD spec-  (Fig. 1f) 28 . In the same spectrum, the absence of the (002) crystal plane at 2θ = 11.25°for GO (present in the bare GO spectrum; Figure S1, Supporting Information) corresponds to the disrupted GO layers and indicates unstacked graphene sheets 29 . The presence of low-intensity peaks in cl-CS-p (MA) can contribute to the generation of a poorly crystalline material originating from cross-linked chitosan. Additionally, it should be noted that the crystallinity present in CS was decreased in cl-CS-p(MA) due to the effect of the cross-linking and polymerization reactions (Scheme S1, Supporting Information) 30 . Similarly, the Raman spectra ( Figure S2 (Fig. 2c) demonstrates a clearly recognizable, randomly oriented, wrinkled sheet-like structure with high-contrast spherically shaped particles that can be identified as Fe 3 O 4 NPs. In the HR-FE-TEM image, the GO layer is arranged on the exterior surface of the nanocomposite (indicated by arrows) with the Fe 3 O 4 NPs contained in the interior of the material (Fig. 2d). Distinct lattice fringes with an interplanar distance of 0.30 nm were observed and are consistent with the (220) plane of metallic Fe 3 O 4 ( Fig. 2d) 33  , indicating that the C-OH group was effectively grafted and cross-linked (Fig. 3a, b). The C 1 s spectrum of the cl-CS-p(MA)/GO-Fe 3 O 4 NP nanocomposite demonstrates similar effects as those observed for cl-CS-p(MA) with regard to the characteristic peaks of these materials (Fig. 3c). However, the altered peak intensity of C-C/C-H was observed in the spectrum of cl-CS-p(MA)/GO-Fe 3 O 4 NPs relative to those of cl-CS-p(MA) and GO ( Fig. 3c; Figure S6a,  Figure S7, Supporting Information). Based on this pH effect, pH 8.5 was chosen for additional experiments. To understand the surface behavior of the nanocomposite material in aqueous solutions, the point of zero charge (pH pzc ) was measured by the pH drift method. As shown in Figure S8 (Supporting Information), the pH pzc of the cl-CS-p(MA)/GO-Fe 3 O 4 NPs was 6.53, indicating that the nanocomposite bears negative surface charges at solution pH > 6.53. Therefore, at pH 8.5, the electrostatic interaction between the cationic MB (C 16 H 18 N 3 S + ) 12 and the anionic cl-CS-p(MA)/ GO-Fe 3 O 4 NPs can predominate and is responsible for the high adsorption efficiency of the material. The adsorption isotherm is critical for interpreting the interactive behavior between the nanocomposite and the MB molecules 40 . The elucidated equilibrium data were fitted using the nonlinear Langmuir model 41 , Freundlich model 42 , and Sips model 43 . The estimated parameters are presented in Table 1 with their associated correlation coefficients. The Langmuir model fits the experimental data better than the Freundlich model. The Sips model, which is a combination of the Langmuir and Freundlich models, was found to be the best-fit model based on the high correlation coefficient of R 2 = 0.9918. At high adsorbate concentrations, the Sips model follows the monolayer adsorption behavior that is characteristic of the Langmuir model 44 . The maximum uptake capacity of 2478 mg/g for MB dye is a significant result with regard to reports for other materials (Fig. 4a and Table S1, Supporting Information) 7,[17][18][19]22,23,[45][46][47][48][49] .
The kinetic efficiency of the adsorbent material allows for the rapid decontamination of toxic organic dyes and offers a prospect for use in the area of real applications. The nanocomposite can easily remove~99% MB dye at equilibrium, which was reached within 20 min of exposure in our studies. After prolonging the contact time to 1 h, the water was completely MB-free ( Figure S9). The obtained kinetic data were suitably fit with a nonlinear pseudo-first-order kinetic model (R 2 = 0.9944) and pseudo-second-order kinetic model (R 2 = 0.9836) (Fig. 4b, Table S2; Supporting Information) 50,51 . The extraordinary uptake capacity and rapid removal of MB are attributed to the synergistic development of the functionalized nanostructured material. To explain this phenomenon, we conducted several adsorption studies by controlling the synthesized products (Fig. 5a). Specifically, pure crosslinked copolymer cl-CS-p(MA) and cl-CS-p(MA)/GO showed low MB dye adsorption performance (Fig. 5a). Meanwhile, the removal of MB by cl-CS-p(MA)/ Fe 3 O 4 NPs was comparable to that of cl-CS-p(MA)/ GO-Fe 3 O 4 NPs, but the recyclability of cl-CS-p(MA)/ Fe 3 O 4 NPs was significantly lower (Fig. 5a). This observation indicates that the role of GO is crucial in the fabrication of a stable and recyclable nanocomposite material. In fact, the sequential syntheses of the crosslinked chitosan and stabilized GO nanosheets and further cross-linking with the Fe 3 O 4 NPs constitute a deliberate approach toward producing a structurally stable material with many well-dispersed binding sites that can deliver faster adsorption behavior with higher capacities. It is important to note that the main binding sites for MB adsorption are the carboxylate chains of poly(MA). More insight into the performance of cl-CS-p(MA)/ GO-Fe 3 O 4 NPs toward MB removal can be gleaned by using a combination of XPS, FE-SEM, and elemental mapping analyses. The inclusion of MB within the   Figure S11, Supporting Information) showed micropores with interconnected channels. The specific surface area of the nanocomposite was very small (1.91 m 2 /g) compared with that of porous adsorbents, i.e., activated carbons, which are known to exhibit values up to~3000 m 2 /g. The mean pore diameter of the nanocomposite was 21.83 nm.
Here, it should be noted that the developed nanocomposite possesses a structure that is similar to that of a hydrogel, in which the uniform distribution of active binding sites throughout the hydrogel is crucial for obtaining the observed outstanding adsorption performance, in contrast to a high surface area and/or porosity. The micropores of the nanocomposite are not directly responsible for the adsorption property but instead serve as microchannels for easy penetration of the MB dye.
Herein, the development of interconnected microchannels imparts a shorter diffusion path, enhancing the kinetics of MB uptake. Additionally, the elemental map of sulfur in the MB-adsorbed cl-CS-p(MA)/GO-Fe 3 O 4 NPs displayed the distribution of sulfur on the surface of the nanocomposite, signifying the uptake of MB (Fig. 5d). The surface adsorption of MB dye on the cl-CS-p(MA)/ GO-Fe 3 O 4 NP nanocomposite was further confirmed by the presence of sulfur in the EDS spectra of MB-adsorbed cl-CS-p(MA)/GO-Fe 3 O 4 NPs ( Figure S12, Supporting Information). It is important to note that the microchannels were active throughout the entire contact time and that even after the fifth adsorption-desorption cycle, the pores were capable of uptaking the cationic MB dye. Furthermore, the separation of the adsorbed dye from (i.e., the regeneration of) the MB-adsorbed swollen cl-CS-p(MA)/GO-Fe 3 O 4 NPs was achieved with a simple approach, namely, by changing the pH of the aqueous media. Moreover, the substrate could be regenerated at least five times through an adsorption-desorption cycle by using an external magnet or spatula, achieving an adsorption efficiency that was greater than~97% (Figure S13, Supporting Information). The magnetic hysteresis of the cl-CS-p(MA)/GO-Fe 3 O 4 NPs was measured, and the saturation magnetization was found to be 6.1 emu/g, demonstrating magnetic separation ability ( Figure S14, Supporting Information). After obtaining such promising results in the removal of MB from synthetic wastewater, we checked the stability of the adsorbate material (cl-CS-p(MA)/GO-Fe 3 O 4 NPs) under different experimental conditions such as pH 9 ± 0.5, pH 7 ± 0.5, and pH 3 ± 0.5 at 25°C for 24 h to investigate its suitability in practical applications. The nanostructured material swelled but did not disperse under these experimental conditions, revealing that it possesses both chemical and mechanical stability in the ranges tested (Table S3; Figure S15, Supporting Information). The adsorption behavior of the cl-CS-p(MA)/ GO-Fe 3 O 4 NPs in several dye mixtures was examined. The UV-Vis absorption spectrum of the cationic dye mixture (MB + TB) is shown in Figure S16 (Supporting Information). After adsorption, both MB and TB were completely removed by the cl-CS-p(MA)/GO-Fe 3 O 4 NPs within 10 min. Based on this observation, it can be noted that the developed nanocomposite does not exhibit adsorbent behavior that is specific to MB but can adsorb any positively charged dye. From the practical application point of view, this would be a favorable characteristic of the nanocomposite because it suggests that all types of cationic dyes could be simultaneously removed from wastewater using the developed nanocomposite. In another experiment, we tested the adsorption behavior of the nanocomposite in a mixed-species scenario with an anionic dye, MO, in addition to the cationic dye MB ( Figure S17, Supporting Information). Following this study, the characteristic peak of MB was observed to almost completely disappear, whereas the removal of the anionic MO was not significant (~11%). The inset photograph in Figure S17 shows that the color was due to MO remaining after adsorption and magnetic separation, supporting again our understanding that the main binding mechanism of cl-CS-p(MA)/ GO-Fe 3 O 4 NPs is via electrostatic interaction. Therefore, to clean up wastewater containing both cationic and anionic dyes, an anionic adsorbent should be used in conjunction with the developed cationic adsorbent.

Conclusion
The studies presented here revealed a successful synthesis strategy for the development of a functionalized magnetic nanocomposite adsorbent, cl-CS-p(MA)/ GO-Fe 3 O 4 NPs, with outstanding adsorption performance with dyes. The cl-CS-p(MA)/GO-Fe 3 O 4 NP nanocomposite demonstrated a maximum adsorption capacity of 2478 mg/g, which is the highest reported performance so far. The efficient removal ability of this nanocomposite was likely because of the formation of well-dispersed active binding sites and interconnected microchannels, both of which facilitated rapid adsorption. Furthermore, the cl-CS-p(MA)/GO-Fe 3 O 4 NP nanocomposite was stable over a wide range of pH values, and after adsorption, the cl-CS-p(MA)/GO-Fe 3 O 4 NPs could be separated using a magnet or spatula. These outstanding properties make cl-CS-p(MA)/GO-Fe 3 O 4 NPs an attractive candidate material in the field of water environmental remediation.