Methylene Blue Adsorption Properties Research Articles

Lignin-Derived Sustainable Nano-Platforms: A Multifunctional Solution for an Efficient Dye Removal.

In contrast to conventional non-biobased adsorbents, lignin emerges as a cost-effective and environmentally benign alternative for water treatment. This study identifies unexpected and unpredicted multifunctional properties of lignin nanoparticles (LNPs). LNPs, which are prepared by simple physical processes, demonstrated for the first time to behave as multifunctional materials able to adsorb and photodegrade methylene blue (MB) in aqueous medium upon UV irradiation. Furthermore, the synthetic approach adopted to synthesize LNPs - and therefore their surface properties - strongly affects their performances. More specifically, LNPs obtained by solvent-antisolvent nanoprecipitation (SLNPs) show the highest MB adsorption properties (98 % removal), reaching a maximum adsorption capacity of 43.0 mg g-1, and the fastest adsorption kinetics with respect to other lignin-based adsorbents. Conversely, hydrotropic LNPs (HLNPs) exhibit exceptional photocatalytic activity, resulting in 98 % MB degradation over 6 hours of UV irradiation, combined with the ability to be easily recycled and reused. The present effort paves the way for the use of LNPs as efficient multifunctional materials able to perform concurrently adsorption and photocatalytic degradation of dye pollutants, toward the creation of a sustainable biobased water treatment platform.

Preparation of magnetic activated carbon fibers@Fe3O4 by electrostatic self-assembly method and adsorption properties for methylene blue.

Nano-Fe3O4 was loaded onto coconut-based activated carbon fibres (CACF) using an electrostatic self-assembly method. The effects of the mass ratio of CACF to nano-Fe3O4, loading time, pH and temperature on the loading effect were investigated and ideal loading conditions were determined. To study the adsorption performance of MACF@Fe3O4 for methylene blue, the effects of the initial concentration, pH and time on the adsorption were investigated and the working conditions of adsorption were established. MACF@Fe3O4 was systematically characterized. Adsorption kinetics were investigated under ideal conditions. The ideal loading conditions for MACF@Fe3O4 were as follows: mass ratio of 1:1, 20 min, pH 9.36, 22.5°C. The saturation magnetization of MACF@Fe3O4 was 48.2263 emu·g-1, which could be quickly separated under an external magnetic field. When the dosage was 0.010 g, the adsorption rate reached 97.29% and the maximum adsorption capacity was 12.1616 mg·g-1. The adsorption process conformed to pseudo-first-order kinetics during the first 15 min and pseudo-second-order kinetics during 20-120 min. The equations were and , respectively. The isothermal adsorption model showed that MACF@Fe3O4 was more in line with the Langmuir model, indicating that the adsorption process was mainly monolayer adsorption. The thermodynamic analysis results showed that the adsorption process of MB by MACF@Fe3O4 was an endothermic process. In this study, MACF@Fe3O4 with high adsorption capacity and easy separation from coconut palm fibres has good application prospects in the field of adsorption, which can promote the high-value utilization of coconut palms.

Functional properties and continuous adsorption process of Arenga pinnata shell and its porous biochars for aqueous methylene blue removal

Arenga pinnata shell, an agricultural-processing residue, was used as an alternative precursor for synthesizing Arenga pinnata shell particles (ASP), Arenga pinnata shell biochar (ASB), and Arenga pinnata shell activated biochar (ASAB) for methylene blue (MB) adsorption. Optimized adsorbent was observed for ASAB fabricated via an impregnation ratio of KOH to ASP of 0.5:1 (w/w) at 700 °C for 30 min of activation time under N2 pyrolysis, with a surface area, pore volume, and average pore diameter of 967 m2/g, 0.572 cm3/g, and 2.47 nm, respectively. The adsorbent also possesses the largest carbon constituent (90.4 %), negative surface charge (−36.4 mV), and abundant oxygen-containing functional groups. Dynamic MB adsorption properties on the adsorbents from the aqueous environment under continuous mode at 25 °C were determined using the Thomas and Yoon-Nelson models. Although the ASP and ASB presented comparatively favorable adsorption properties, the optimum adsorption performance was observed for the ASAB. Its superior functional features contributed to the largest adsorption capacity of 203.86 mg/g. The elemental composition analysis indicated the presence of sulfur on the ASAB surface, which supported the findings. This research demonstrates the utility of Arenga pinnata shell as an eco-friendly precursor for high-performance adsorbent fabrication with excellent MB adsorption properties.

Zeolite/slag-based porous geopolymer sphere regenerable composites with enhanced mechanical strength and good dye removal performance

Porous slag-based geopolymer spheres were synthesized by a suspension-solidification method using silicone oil as suspending bath. Zeolite powder, expected to improve or optimize the mechanical and/or adsorption properties, was used as second phase. The porous morphology, structure change, specific surface area, porosity, mechanical properties as well as adsorption capacity of the porous solid waste-based sphere composites were investigated. The mechanical strength was significantly improved by the addition of zeolite, along with a slight decrease for methylene blue adsorption properties. The obtained porous slag-based zeolite/geopolymer spheres with high porosity and acceptable strength have potential application as low cost and high effective adsorption composite materials.

Chitosan-polyvinyl alcohol-diatomite hydrogel removes methylene blue from water

Dye pollution in the aquatic environment can harm ecosystems and human health. Here, we developed a new green adsorbent by applying an improved drying process. Diatomite was embedded in a network structure formed between chitosan and polyvinyl alcohol without using any crosslinking agent to prepare chitosan-polyvinyl alcohol-diatomite hydrogel beads through alkali solidification. The beads were tested for removing a cationic dye (methylene blue (MB)) from water. The structure of the adsorbent beads was analysed using scanning electron microscopy, energy-dispersive spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and Fourier-transform infrared spectroscopy. The adsorption capacity was investigated, and the results indicated excellent MB adsorption properties. The adsorbents had a rough surface and high swelling capacity of 66.9 g/g. The maximum MB adsorption capacity was 414.70 mg/g, and the adsorption followed the Freundlich isothermal and quasi-second-order kinetic models. The adsorption was an endothermic spontaneous process governed by both intra-particle and external diffusion processes. The proposed adsorption mechanisms involved hydrogen bonding and electrostatic interactions. These adsorbent beads have considerable application potentials owing to their high adsorption capacity, green composition, and non-polluting nature.

Adsorption property and kinetic studies of activated carbon fibers prepared from tissues by CO2 activation

Well-developed micro and mesoporous activated carbon fibers (ACFs) with fiber structure were prepared from tissue by CO2 activation. The XRD patterns and Raman spectrum indicated ACFs had a graphitic and amorphous structure. The SEM results indicated that the sample exhibited fiber structure with lots of mesoporous, with an average pore size of 2-5 nm. The specific surface area of 1517 m2 /g, micro surface area of 412.9 m2 /g, and total pore volume of 1.194 cm3 /g were obtained at 900°C with CO2 activation for 2 hours. ACFs showed relatively high methylene blue adsorption properties with an equilibrium adsorption capacity of 526 mg/g. The kinetic model of the Pseudo-second-order equation was more suitable for MB adsorption than the Pseudo-first-order equation and Intraparticle diffusion kinetics, with a high correlation coefficient value (R>0.999). The present research provided a new idea of bionics for the manufacture of ACFs and brought forward a creative prospect for achieving energy-related CO2 emissions to net-zero and mitigating global warming.

Improvement of methylene blue adsorption properties of lemon peel by surface modification

In this study, methylene blue adsorption properties of lemon peel (LP), as agricultural waste, was improved by surface modification. Surface modification of the LPs was achieved by applying sulfuric acid (H2SO4) in the ratio of 1:1, 1:2, and 1:3 w/w. Adsorption success of surface modification was determined by the measurement of methylene blue solution with UV-VIS. Adsorption results were obtained at various concentration to apply for kinetic and isotherms equations. Also, surface functional groups and surface morphological properties of raw and modified LP were examined by FT-IR spectrometer and scanning electron microscope (SEM) before and after adsorption. Methylene blue adsorption capacity of LP after modification (200 mg/g) increased roughly 2.5 times compare to those in raw peel. The most suitable isotherm (R2=0.998) and kinetic models (R2=0.999) were determined as Langmuir Type I and Pseudo-second-order, respectively. Limited changes in FT-IR spectra was observed (-OH, -CH3, -C=O, -COOH).

Synthesis, Swelling, Diffusion and Cationic Dye Adsorption Studies of Semi‐IPN Sodium Alginate/ Poly(HEMA‐co‐MA) Hydrogels

AbstractIn this study, the novel pH‐sensitive s‐IPN consist of sodium alginate integrated with poly(HEMA‐co‐MA) hydrogel matrix are prepared by using two‐step methodology. In the first step, 2‐hydroxyethyl methacrylate (HEMA)/maleic acid (MA) copolymeric hydrogels are prepared by gamma radiation polymerization. Then, poly(HEMA‐co‐MA) hydrogel was immersed in sodium alginate solution (SA) and finally gamma radiation polymerization was carried out. The swelling, pH‐sensivity and diffusion properties of the prepared s‐IPN gels in deionized water and in dye solutions were investigated. Methylene Blue (MB) was used as a model dye. MB adsorption capacities of the hydrogels were found to be 0.26, 0.40 and 13.77 mg MB/g dry gel in PHEMA, P(HEMA‐co‐MA) and s‐IPN SA/P(HEMA‐co‐MA) hydrogels, respectively. MB release data was fitted to various kinetic models to study the dye release behavior. The MB release from all the prepared hydrogels fitted the Korsmeyer‐Peppas model. Swelling, diffusion and MB adsorption properties of the new s‐IPN hydrogel were improved with the inclusion of SA and MA in the gel structure.

Nanoporous Carbon Materials from Terminalia bellirica Seed for Iodine and Methylene Blue Adsorption and High-Performance Supercapacitor Applications

Abstract Here we report the methylene blue adsorption and energy storage supercapacitance performances of the nanoporous activated carbons obtained by the zinc chloride (ZnCl2) activation of biowaste, Terminalia bellirica (Barro) seed stone. The activation was performed at lower temperatures (400–700 °C) under an inert nitrogen gas atmosphere. The total specific surface area and pore volume range from 1077 to 1303 m2 g−1 and 0.752 to 0.873 cm3 g−1, depending on the carbonization temperature. Due to the well-developed porosity, the sample with optimal surface area showed excellent iodine and methylene blue adsorption properties with a maximum iodine number and methylene blue value of 909.8 mg g−1 and 357.2 mg g−1, respectively. Batch adsorption studies revealed that the optimum methylene blue adsorption is favorable in an alkaline medium, with a contact time of 270 min and an adsorbent dose of 8 g L−1, respectively. The Langmuir isotherm model could best explain the equilibrium adsorption with a monolayer adsorption capacity of 312.5 mg g−1. The electrochemical measurements performed in a three-electrode system revealed a high specific capacitance of 319 F g−1 at 1 A g−1. Furthermore, the electrode retained 46% capacitance at 50 A g−1 with an excellent cycle life of 98.5% after 10,000 consecutive charging/discharging cycles. These results imply that a biowaste Terminalia bellirica seed has a considerable potential to produce high surface area porous carbons materials desired in adsorption technology and high-performance supercapacitor applications.

The Potential of Waste Phloem Fraction of Quercus cerris Bark in Biochar Production

Quercus cerris phloem is a lignocellulosic waste fraction obtained from bark fractionation. Biochars are technologically interesting functional materials that may be produced from lignocellulosic solid materials. This study explores the solid material properties of Quercus cerris phloem, evaluates biochar production from it, and explores its application as an adsorbent. In the first part of the study, thermogravimetric analysis, SEM microscopy observations, FT-IR spectroscopy, and ICP-AES analyses were performed on raw Quercus cerris phloem. In the second part of the study, biochars and activated carbons were produced and their structure, surface functional groups, methylene blue adsorption properties, and specific surface areas were determined. The results showed that Quercus cerris phloem is a lignocellulosic solid material that decomposes in a wide temperature range between 265 and 765 °C. The activation energy of phloem pyrolysis ranged between 82 and 172 kJ mol−1 in pyrolysis. The mineral composition is mainly calcium (88%) and potassium (4%). The biochar yield of Quercus cerris phloem ranged between 28% and 42% at different moderate temperature–time combinations. Raw phloem, phloem biochars, and phloem-activated carbons show high methylene blue removal efficiencies. Methylene blue adsorption follows pseudo-second-order kinetics. The BET surface areas of Quercus cerris phloem-activated carbons varied between 262.1 m2 g−1 and 317.5 m2 g−1.

Preparation and Modification of Rape Straw Biochar and Its Adsorption Characteristics for Methylene Blue in Water

To solve the double problems of methylene blue (MB) pollution in water and waste of straw resources, rape straw biochar (RSB600) was made by thermal decomposition of discarded rape residues at 600 °C, and modified RSB600(M-RSB600) was prepared after treatment with NaOH for MB adsorption. The physicochemical properties, MB adsorption properties and mechanism of RSB600 and M-RSB600 were studied. According to the experimental findings, M-RSB600 has stronger aromaticity, higher hydrophilicity, and more polarity than RSB600. Under the same adsorption conditions, M-RSB600 obtained better MB adsorption effect with less dosage. The MB equilibrium adsorption capacity of M-RSB600 reached 268.46 mg/g, which was 65.6% higher than that of RSB600. The quasi-second-order kinetic model better described the adsorption kinetics of MB on RSB600 and M-RSB600 (R2 > 0.98), and the Freundlich and Temkin models better described the adsorption isotherms (R2 > 0.95). The adsorption process was spontaneous, internal heat and entropy driven multilayer adsorption, dominated by chemical adsorption, specifically involving multiple interaction mechanisms, including electrostatic adherence, hydrogen-bond, π-π bond and ion-exchange. The results demonstrated that NaOH modification obviously improved the structure of RSB and make it had better adsorption and regeneration performance. M-RSB600 can be utilized as the ideal substance for effectively removing MB from effluent.

Porous alkali‐activated material from hypergolic coal gangue by microwave foaming for methylene blue removal

AbstractOverall, 100% hypergolic coal gangue (HCG)‐based geopolymer foams were produced by a novel saponification‐microwave foaming combined route. Microwave foaming with and without expired vegetable oil was first used to produce CG‐based geopolymer foams. Macropores were mainly generated by microwave foaming, and mesopores were mainly obtained by the addition of expired soybean oil that underwent a saponification reaction. The effects of the oil content on the density, porosity, pore morphology, compression strength, and methylene blue adsorption properties were studied. High total porosity (85.9–89.0 vol%) and acceptable compression strength (0.46–1.1 MPa) HCG‐based geopolymer foams were produced. Foams with 12.59 wt% oil exhibited the best adsorption properties, with an adsorption capacity up to 9.4 mg/g and high removal efficiency of about 95.3%. These solid‐waste‐based porous components are promising monolithic adsorbents for wastewater treatment.

Adsorption of Methylene Blue on Azo Dye Wastewater by Molybdenum Disulfide Nanomaterials

In this study, flower-like MoS2 nanomaterials were synthesized by hydrothermal method with excess thiourea. The adsorption performance of MoS2 adsorbent for methylene blue (MB) in azo dye wastewater was studied. The morphology, crystal phase, and microstructure of nano MoS2 samples were characterized by X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, and Fourier transform infrared spectroscopy. The effects of adsorption isotherm, kinetics, different hydrothermal time, and pH on the adsorption experiment were studied. The results showed that the MoS2 adsorbent with a hydrothermal time of 1 h had good adsorption properties for MB. The adsorption data accord with the Langmuir isotherm model, and the maximum adsorption capacity of MoS2 adsorbent is 200 mg/g, and the adsorption kinetics agrees well with the pseudo two-level model. The removal rate of MB is not significantly affected by the pH values. The large pH range can still maintain the removal rate above 93.47%, and the regeneration and recovery properties of MoS2 were also explored. Finally, the adsorption mechanism of MoS2 on MB is discussed.

Co-pyrolysis of sewage sludge and sodium lignosulfonate: Kinetic study and methylene blue adsorption properties of the biochar

Co-pyrolysis of sewage sludge (SS) and lignin is a promising method to dispose of SS and obtain valuable biochar, however, the synergy effect has been rarely reported. In this paper, lignin of sodium lignosulfonate (SL) was blended with SS for co-pyrolysis. Thermogravimetric analyzer/differential scanning calorimetry (TGA/DSC) was used to investigate the reaction kinetics during co-pyrolysis. And the adsorption performance of co-pyrolysis biochar on methylene blue (MB) was determined. Results showed that the SS decomposition was promoted with SL addition. Kinetic analysis using the Coats-Redfern method indicated the reaction order model to be the primary pyrolysis kinetic mechanism. The synergistic effect of promotion was caused by catalytic metals, and inhibition was caused by ash and tar adhesion. The specific surface area of biochar was improved during co-pyrolysis from 62.53 to 243.22 m2 g−1, while SL ratio of 80% achieved the maximum specific surface area. Co-pyrolysis showed an inhibition effect on porosity formation when SL ratio was below 60%, while a promotion effect was found when SL ratio exceeded 60%. Co-pyrolysis elevated the MB adsorption capacity of SS-derived biochars from 12.48 to 154.06 mg g−1, and was indicated as a promising method for adsorbents production.

High Surface Area Nanoporous Activated Carbons Materials from Areca catechu Nut with Excellent Iodine and Methylene Blue Adsorption

Nanoporous carbon materials from biomass exhibit a high surface area due to well-defined pore structures. Therefore, they have been extensively used in separation and purification technologies as efficient adsorbents. Here, we report the iodine and methylene blue adsorption properties of the hierarchically porous carbon materials prepared from Areca catechu nut. The preparation method involves the phosphoric acid (H3PO4) activation of the Areca catechu nut powder. The effects of carbonization conditions (mixing ratio with H3PO4, carbonization time, and carbonization temperature) on the textural properties and surface functional groups were studied. The optimum textural properties were obtained at a mixing ratio of 1:1, carbonized for 3 h at 400 °C, and the sample achieved a high specific surface area of 2132.1 m2 g−1 and a large pore volume of 3.426 cm3 g−1, respectively. The prepared materials have amorphous carbon structures and contain oxygenated surface functional groups. Due to the well-defined micro-and mesopore structures with the high surface area and large pore volume, the optimal sample showed excellent iodine and methylene blue adsorption. The iodine number and methylene blue values were ca. 888 mg g−1 and 369 mg g−1, respectively. The batch adsorption studies of methylene dye were affected by pH, adsorbent dose, contact time, and initial concentration. The optimum parameters for the methylene blue adsorption were in alkaline pH, adsorbent dose of 2.8 g L−1, and contact time of 180 min. Equilibrium data could be best represented by the Langmuir isotherm model with a monolayer adsorption capacity of 333.3 mg g−1. Thus, our results demonstrate that the Areca catechu nut has considerable potential as the novel precursor material for the scalable production of high surface area hierarchically porous carbon materials that are essential in removing organic dyes from water.

Radiation‐initiated chitosan‐based double network hydrogel: Synthesis, characterization, and adsorption of methylene blue

AbstractA novel chitosan (CTS)‐based double network Poly(2‐acrylaMido‐2‐Methyl‐1‐propanesulfonic acid)/Polyacrylamide/CTS hydrogel was synthesized by irradiation initiated. Laponite RD (RD) was used as both dopant and the cross‐linking agent. Then the fabricated hydrogel was applied as an efficient adsorbent to remove the methylene blue (MB) in an aqueous solution. This hydrogel has both high strength and good adsorption properties for MB. The results from Brunauer–Emmett–Teller method confirmed that the hydrogel has a large specific surface area (96 m2/g) and developed pore structure, which is available for the contact between the adsorbent and dye molecules. In the adsorption process, the RD provides plenty of negative charges as adsorption sites for MB molecules. The influence of pH, temperature, and adsorbent dose on the adsorption performance was investigated in detail. The experimental data fit well with the pseudo‐second‐order kinetic model and Langmuir isotherm. Besides, the mechanical strength of the hydrogel was also investigated in this work.

Preparation of β-cyclodextrin/graphene oxide and its adsorption properties for methylene blue

Graphene oxide (GO) and GO-based materials have shown excellent adsorption properties because of bounteous structure and rich oxygen functional groups. Many studies have shown that GO are utilized as adsorbents to remove organic dyes from wastewater. GO was prepared by modified Hummers method using graphite powder as raw material. On this basis, β-cyclodextrin/graphene oxide composite (β-CD/GO) was prepared by modifying graphene oxide via β-cyclodextrin(β-CD) crosslinking method. GO and β-CD were characterized by Fourier transform infrared spectroscopy (FT-IR), energy-dispersive X-ray (XRD), scanning electron (SEM) and thermogravimetric analysis (TGA). Their adsorbents properties have been studied with methylene blue (MB) as adsorbate. The factors affecting the study include the temperature, adsorption time, amount of adsorbent and system pH value. Adsorption isotherm and kinetics of the adsorption process are systematically analyzed. The results show that β-CD/GO has a different adsorption capacity from GO under the same adsorption factors. Under the optimized conditions (the reaction temperature is 70 °C, the reaction time is 60 min and the concentration of adsorbent is 0.04 g/L), the removal efficiency of β-CD/GO is 20% higher than that of GO from 70% to 90%. The maximum adsorption capacity of β-CD/GO is 76.4 mg/g. β-CD/GO can be effectively regenerated by elution with absolute alcohol. In these tests, β-CD/GO was suggested to be more efficient than GO in the removal of organic dyes.

Preparation of cellulose/sodium alginate/sepiolite porous microspheres and their adsorption properties for methylene blue

To improve the feasibility of cellulose microspheres for application in wastewater treatment, microcrystalline cellulose/sodium alginate/sepiolite (MSS) composite porous microspheres were synthesized via a two-step method of self-assembly and suspension droplet. The as-prepared MSS microspheres were characterized by SEM, FT-IR and XRD analyses, and the results display that the MSS microspheres possess a layered cross-linked porous structure. Parameters affecting dye uptake (such as pH and sepiolite content) were evaluated, and pH of 7 and MSS-30 microsphere were taken as the optimal removal environment and adsorbent. The maximum adsorption capacity of MSS-30 microsphere was found to be 319.5 mg/g, indicating an efficient and feasible adsorbent for MB removal from wastewater.

Preparation of Chitosan/Polyacrylamide/Graphene Oxide Composite Membranes and Study of Their Methylene Blue Adsorption Properties.

This thesis reports the preparation of chitosan/polyacrylamide/graphene oxide nanocomposites (CAGs) and a study of its adsorption properties of methylene blue (MB) solution. Initially, we synthesized CAGs by blending and freeze-drying methods. Then, we conducted a series experiments by removing MB from aqueous solution to test its adsorption properties and adsorption mechanism. We used UV-Vis spectrophotometry to determine the concentration of residual methylene blue accurately and efficiently, which has a specific absorption peak at 662 nm in the UV-Vis spectrum, in aqueous solution. When the graphene oxide content in the composite was 20 wt%, the adsorption capacity reached maximum values. The chemical properties and surface structure of the nanomaterials were analyzed using FT-IR, TGA, SEM, and BET. Also, we carried out experiments to measure the adsorption properties of the CAGs by varying several factors, such as initial concentration, adsorption time, and pH, etc. The outcomes revealed that the adsorption equilibrium was developed after 2800 min at 20 °C (room temperature) with an adsorbent dosage of 0.01 g mL−1. The ion adsorption equilibrium data were well-fitted by the Langmuir isotherm with a maximum monolayer capacity of 510.2 mg/g. Kinetic researches disclosed that the adsorption procedure was defined by a pseudo-second-order model. Thermodynamic researches revealed that the enthalpy change (ΔH 0) as well as Gibbs free energy change (ΔG 0) of the adsorption procedure was negative, indicating that the adsorption procedure was spontaneous and exothermic. After three cycles, the removal efficiency was still 90.18%. Therefore, in conclusion, we believe that the CAGs is a good adsorption material for organic dyes due to its good adsorption and recyclable properties.

Preparation of sulfonate chitosan microspheres and study on its adsorption properties for methylene blue

Dyes bring a lot of benefits to our lives, however, as common organic pollutants, they have destructive influences on the environment. Firstly, glutaraldehyde crosslinked chitosan microspheres (GCS) are prepared via inverse-phase suspension polymerization. Then, GCS microspheres are acted as the base material, ammonium persulfate (Aps) as the initiator, sodium styrene sulfonate (SSS) as anionic functional monomer, functional microspheres (GCS-g-PSSS) are prepared by surface grafting polymerization. The amount of monomer and Aps, temperature and reaction time is respectively explored. The chemical structures and physicochemical properties of functional microspheres were characterized by FT-IR, zeta potential, scanning electron microscope and X-ray photoelectron spectroscopy. The adsorption kinetic at different temperature and initial concentration is studied and fitted. The adsorption isotherms of GCS-g-PSSS for MB are explored at different pH, temperature and salinity. The adsorption capacity of GCS-g-PSSS for MB is 820.1 mg/g at 318 K. The adsorption isotherms at different temperature are fitted by Langmuir, Freundlich, Dubinin-Radushkevich and Temkin. Thermodynamic parameters imply that adsorption is a spontaneous and endothermic process. And this adsorbent has good reusability. The adsorption ability of GCS-g-PSSS microspheres is also excellent for other cationic dyes. Thus, GCS-g-PSSS microspheres might serve as a promising adsorbent for contaminated water scavenging.