ABSTRACT Utilizing Glutaraldehyde crosslinked sodium carboxymethyl cellulose (CMC-GA) hydrogel and its nanographene oxide composite (CMC-GA-GOx), an effective carboxymethyl

cellulose-graphene oxide biobased composites adsorbent was developed for the adsorption removal of methylene blue (MB) cationic dye contaminate from industrial wastewater. The CMC-GA-GOx

composites developed were characterized using FTIR, RAMAN, TGA, SEM, and EDX analysis instruments. Through batch experiments, several variables affecting the removal of MB dye, including the

biocomposites GO:CMC composition, adsorption time, pH and temperature, initial MB concentration, adsorbent dosage, and NaCl concentration, were investigated under different conditions. The

adsorption capacity of 76.92 mg/g. The adsorption process followed the kinetic model of pseudo-second order. The removal of MB was exothermic and spontaneous from a thermodynamic

standpoint. In addition, thermodynamic results demonstrated that adsorption operates most effectively at low temperatures. Finally, the reusability of the developed CMC-GA-GO102 has been

proved through 10 successive cycles where only 14% of the MB dye removal percentage was lost. These results suggest that the developed CMC-GA-GO102 composite may be an inexpensive and

reusable adsorbent for removing organic cationic dyes from industrial wastewater. SIMILAR CONTENT BEING VIEWED BY OTHERS ADSORBENT BASED ON MOF-5/CELLULOSE AEROGEL COMPOSITE FOR ADSORPTION

OF ORGANIC DYES FROM WASTEWATER Article Open access 07 July 2024 NOVEL AMINO-ETHYL CARBOXYMETHYL CELLULOSE CROSSLINKED AMPHOLYTE HYDROGEL DEVELOPMENT FOR METHYL ORANGE REMOVAL FROM WASTE

WATER Article Open access 26 June 2024 EXPERMENTAL INVESTIGATION ON ADSORPTION OF METHYLENE BLUE DYE FROM WASTE WATER USING CORNCOB CELLULOSE-BASED HYDROGEL Article Open access 24 February

2024 INTRODUCTION Water is one of the essential elements for all life on earth, and it has been a boon to human civilization since ancient times. However, water is one of the most

challenging environmental issues, and supplying safe, affordable drinking water and clean water is a global challenge. The swiftly deteriorating environmental contamination of natural

resources is a contemporary issue that must be addressed immediately if the earth and its inhabitants are to endure for future generations1,2. Large quantities of water have become

contaminated in recent years due to the rapid development of various technological fields, leading to increased environmental disturbances and severe pollution issues3. In general, water

pollution can occur in a variety of ways; however, a significant amount of water pollution is caused by the contamination with dyes as a result of numerous industrial effluents from paper,

cosmetics, leather, pigments, petroleum, textiles, plastic, refineries, printing, pharmaceutical, and food processing industries4,5,6. According to their dissociation behavior in aqueous

solutions, dyes can be divided into three categories: (a) anionic (acid, direct, and reactive dyes) with a negative charge primarily owing to the (SO3) group, (b) cationic (basic dyes) with

a protonated amine group, and (c) nonionic (disperse dyes)7. Cationic or anionic azo dyes contain one or more azoic bonds (N=N). In addition to its resistance to light, heat, and aerobic

digestion, it can cause acute diseases such as genetic mutation, allergic reactions, vomiting, and cyanosis8, resulting in environmental pollution and attendant health concerns for all

living organisms, including humans, animals, and plants9,10,11. These dyes adversely affect human health due to their chemical stability and nonbiodegradability. Previous research has

demonstrated that cationic dyes are highly toxic and more harmful than anionic dyes because they readily interact with cytoplasm12,13,14,15. Methylene blue (C16H18N3ClS) is both a thiazine

and cationic dye. MB is predominantly used as a colorant in the textile industry, particularly in wool, silk, and cotton dyeing. It is widely used in industrial processes, including

biomedical pigments for cell staining, paper printing and pulp, rubber, plastics, leather, cosmetics, and textile coloring. Due to its toxicity, carcinogenicity, mutagenicity, and

nonbiodegradability, it is considered the most harmful organic pollutant in the water environment. It can cause nausea, mental confusion, vomiting, eye burns, mental confusion, cyanosis,

high blood pressure, tachycardia, abdominal pain, skin irritation, methemoglobinemia, red blood cell breakdown, dyspnea, profuse sweating, gastrointestinal irritation, allergic reaction,

diarrhea in humans. Additionally, its inhalation causes shortness of breath after brief exposure13,16,17,18. Dyes-contaminated wastewater is more challenging to manage due to its complex

chemical composition, including inorganic filler, organic solvent, polymer, and toxic dyes. Therefore, removing toxic dyes from the effluent is a pressing concern. Before discharging

industrial effluent into water streams, removing these contaminants and reducing the concentration of these dyes is essential. Current dye-polluted wastewater treatment methods include

adsorption, oxidation, coagulation, electrolysis, photocatalytic degradation, biodegradation, and liquid membrane separation. Due to the complex aromatic structures of dyes, which make them

highly stable, conventional dye removal techniques are frequently ineffective. Adsorption is a process that researchers and industry are interested in because of its low cost, ease of

regeneration, and availability of various adsorbents. It has recently received much attention due to its low cost, ease of regeneration, and availability of various adsorbents. It is now

considered a simple, more accessible, economical, eco-friendly, and effective technology for removing various dyes19,20,21. Numerous organic and inorganic adsorbents, such as ion exchange

resins, fly ash, carbon-based materials, mesoporous silica, polysaccharides, zeolites, clays, and hydrogel nanocomposites, have been studied for the removal of dyes. However, they have

disadvantages such as low adsorption capacities, low selectivity, and high cost. Therefore, efforts are being made to develop versatile, cost-effective, and efficient adsorbents for water

purification applications22,23. For wastewater remediation, a natural polymer such as polysaccharide has received much attention for environmental reasons. Due to their economic viability

and environmental significance, polysaccharides such as starch, chitosan, alginate, and carboxymethyl cellulose have been extensively used as efficient adsorbents in wastewater treatment

fields due to their economic viability and environmental significance24. In addition, they are remarkably inexpensive, abundant, and biocompatible. Carboxymethyl cellulose (CMC) is an

anionic linear polysaccharide derived from cellulose that contains (–CH2–COOH) groups linked to the (OH) groups of glucopyranose monomers, which form the cellulose backbone, and a high

number of active functional groups including hydroxyl and carboxyl groups that serve as desirable active sites during the adsorption process. It is the most popular and environmentally

preferred polymer that is water-soluble. It typically contains significant amounts of active functional groups, such as hydroxyl and carboxyl, which are desirable active sites during

adsorption. CMC is also an inexpensive, non-toxic, biodegradable, and renewable polymer25,26,27. However, CMC has weak mechanical properties and a low adsorption capacity despite its

extensive use in wastewater treatment. Several physical and chemical modification techniques for CMC, such as composite formation and grafting, have been devised to overcome these

drawbacks28,29. On the other hand, graphene oxide (GO) is produced by the thermal oxidation of the two-dimensional carbon allotrope graphene, which is a highly motivating material. Various

oxygen functional groups (–OH, –O–, –COOH, diol, etc.) are located on the surface and edges of graphene oxide, leading to its widespread use in adsorption for wastewater treatment. These

properties include a large specific surface area, low toxicity, high ionic exchange, biocompatibility, and high hydrophilicity. So, graphene oxide (GO) is presently used as an adsorbent

material for various pollutants in wastewater, including heavy metals and dyes. However, it is challenging to separate GO after adsorption, so several experiments have been conducted to

combine GO and CMC to form an effective structure of GO/CMC-based composites for future applications30,31,32. In response to this interest, a study was conducted to develop an effective

carboxymethyl cellulose-graphene oxide biobased composites adsorbent for removing cationic MB dye using Glutaraldehyde-bonded sodium carboxymethyl cellulose (CMC-GA) hydrogel and graphene

oxide (CMC-GA-GO). This study investigates the merging of different approaches for modifying carboxymethyl cellulose with GO to enhance its sorption of MB dye. These approaches include the

followings: * 1. Chemical crosslinking of the CMC to create a three-dimensional porous structure with improved mechanical properties and surface area, * 2 Physical crosslinking through the

free drying technique creates additional porosity and internal surface area, * 3. It induces additional adsorption sites by mixing GO particles with additional surface area. Finally, we have

obtained novel physical and chemical crosslinked CMC-GA-GOx composites with high porosity, surface area, and appreciated numbers of active sites for removing cationic dye from aqueous

solution. The CMC-GA-GOx was characterized using FTIR, RAMAN, XRD, SEM, TEM, EDX, and TGA. The contact time, initial dye concentrations, adsorbent dosage, pH, temperature, and other

adsorption batch conditions were investigated. In addition, isotherms, kinetics, and adsorption thermodynamics parameters were determined. MATERIALS AND METHODS MATERIALS Sodium

carboxymethyl cellulose (CMC) was obtained from Across (99%), graphite (200 mesh, 99.99%) was purchased from Alpha Aesar), sulfuric acid (95–97%) was obtained from Riedel deHaen). Potassium

permanganate (99%, Long live), and glutaraldehyde (GA; 25%) were acquired from Sigma Aldrich. Hydrochloric acid (HCl; 30%) was obtained from El Salam for Chemical Industries, Egypt. Sodium

hydroxide, hydrogen peroxide (H2O2; 36%) were obtained from Pharaohs Trading and Import, Egypt. Methylene blue (MB) was used (99%, Sigma-Aldrich). All chemicals were used exactly as they

were delivered.and all other prepared solutions were made with distilled water (2108, GLF, Germany). PREPARATION OF GO Our previous research mentioned that graphene oxide was synthesized

using the Hummers' method33. Briefly, 3.0 g of graphite powder was added to a 70 mL solution of concentrated sulfuric acid in a 150 mL glass beaker while agitating for 10 min. This

suspension was kept at 20 °C in a water bath while 9.0 g KMnO4 was steadily added. Afterward, 3.0 g of potassium persulfate was added progressively. Afterward, the mixture's temperature

was increased to 40 °C with vigorous stirring for approximately half an hour (Slurry A). Next, the Slurry (A) was mixed with 150 mL of water and agitated at 95 °C for 15 min. Then, 500 mL

of water was added to the final slurry (Slurry B), followed by the gradual addition of 15 mL of 30% H2O2, which caused the mixture's color to change from dark brown to yellow. Finally,

the suspension was filtered and rinsed with 1:10 HCl aqueous solutions (250 mL) followed by 250 mL bi-distilled water and dried at 35 °C for 99 h to remove metal ions. The substance obtained

(GO) was used for further research. CONSTRUCTION OF THE CMC-GA 0.3 g CMC powder was dissolved in 30 mL distilled water at room temperature under constant stirring for 24 h. Next, HCl

acidified 0.25 mL glutaraldehyde (25%) was added to the solution as a cross-linker. The mixture was stirred at 300 rpm for 60 min at 30 °C before being lyophilized dried for 48 h using

Christ-freeze dryer Alpha 1-4 LD-2. SYNTHESIS OF CMC-GA-GOX COMPOSITES 0.3 g of CMC was dissolved in 30 mL of distilled water at ambient temperature for three hours with constant stirring.

To ensure a uniform distribution of graphene oxide (GO), 2, 4, 6, and 10 mL of graphene oxide suspension (1.5% w/w) were added to the CMC solution and agitated continuously for 24 h (to

ensure complete dissolution). Then 0.25 mL of HCl-acidified 25% glutaraldehyde was added. At 30 °C, the mixture was stirred for an additional 60 min. The CMC-GA-GOx composites (x = 101, 102,

103, and 105) were obtained (Table 1), and the resulting composites were desiccated using a lyophilizer under the same conditions used to dry the CMC-GA. CHARACTERISTICS Changes in the

morphology of CMC-GA and CMC-GA-GOx composites were examined using a scanning electron microscope (JEOL GSM-6610LV, Tokyo, Japan) at acceleration voltage of 15–20 kV. Specimen surfaces were

coated with a thin layer of gold before observation. Elemental analysis was carried out using the EDX unit. SEM images were obtained at different magnifications. EDX-SEM analysis is

conducted on GO, CMC, CMC-GA, CMC-GA-GO102, and CMC-GA-GO102-MB to determine the elemental composition of the investigated materials and confirm dye adsorption by the investigated

composites. Raman spectroscopy was used to record the Raman spectra of the sample in order to identify the chemical structure changes (BRUKER, OPTIK GMBH, Senterra, Germany).

Thermogravimetric analysis (Shimadzu Thermal Gravimetric Analysis (TGA) 50, Tokyo, Japan) determined the samples' thermal stability under the following operational conditions: 10 °C 

min−1 heating rate in a dynamic nitrogen atmosphere as an inert gas between room temperature and 800 °C. The Fourier Transmission Infrared Spectroscopy (FT-IR) (8400 s, Shimadzu, Kyoto,

Japan), with a range of 400 to 4000 cm−1, was used to detect functional group modifications. The KBr disc method was employed to detect the IR spectra of each sample under investigation.

ADSORPTION RESEARCH In order to assess the adsorption procedure, bulk adsorption experiments were conducted. The desired concentration was attained by dilution, preparing a stock solution of

1000 ppm MB dye by dissolving 0.1 g of each dye in 100 mL of distilled water. In 50 mL of MB dye solution (30 mg/L), 0.02 g of CMC-GA-GO102 composite was accurately inserted. The pH of the

adsorption medium was adjusted between 2 and 11 using 0.1 M solutions of both HCl and NaOH for contact time (0–120 min). Experiments were conducted at a constant rate of agitation (300 rpm)

and a temperature of 25 °C. After it has reached equilibrium, separate the adsorbent from the dye solution by centrifuging it at 3000 rpm for 10 min. At an absorbance wavelength of 662 nm, a

UV–Vis spectrophotometer was utilized to measure the residual concentration of MB dye. Mathematical models of equilibrium and kinetics were developed utilizing the collected data. Without

adjusting the pH, 0.02 g of CMC-GA-GO102 was added under constant agitation to 100 mL Erlenmeyer flasks containing 50 mL of dye solution at the specified concentration (30 mg L−1 of MB). The

isotherms, thermodynamics, and kinetics of adsorption were investigated. The MB dye residual concentration in the aqueous solution was calculated using the initial dye concentration and

absorbance measurements before and after adsorptions. The removal percentage (R%) and adsorption capacities of MB at time t were determined using the following equations: $$R

\left(\%\right)=\frac{{C}_{0- {C}_{t}}}{{C}_{0}}\times 100$$ (1) $$\mathrm{qt }= \frac{({c}_{0}-{c}_{t})v}{1000w}$$ (2) C0 is the initial dye concentration (mg L−1), Ct is the dye

concentration at different time intervals (mg L−1), V is the volume of dye solution (L), and W is the mass of adsorbent (g). R (%) represents the removal efficiency of MB dye using the

adsorbents, and qt is the adsorption capacity (mg/g). ADSORPTION REUSABILITY 0.02 g of CMC-GA-GO102 adsorbent mixed with 50 mL of 10 ppm MB solution of pH 7.0 for 25 min at room temperature

and agitated at 300 rpm. After completion of the adsorption time, the adsorbent was separated from the dye solution by centrifuging it at 3000 rpm for 10 min. The dye removal percentage was

measured as mentioned previously. The CMC-GA-GO102-MB adsorbent was mixed with 100 mL NaCl solution dissolved at DW of 3% concentration at room temperature using a mechanical stirrer at 250 

rpm for 60 min to desorbs MB molecules, then separated as mentioned previously and washed three successive times with distilled water before separating and used in further adsorption

experiments (10 cycles) under the same MB adsorption conditions. RESULTS AND DISCUSSION MATERIALS CHARACTERIZATION FTIR ANALYSIS The chemical structure of GO, CMC, CMC-GA, CMC-GA-GO102, and

CMC-GA-GO102-MB was confirmed by Fourier transform infrared spectroscopy (Fig. 1A). The FT-IR spectrum of GO reveals characteristic peaks at 3425, 2912, 1710, 1589, 1484, 1209, 1021, and

1383 cm−1, corresponding to OH, C–H, C=O, C=C (aromatic ring), O–C=O, epoxy C–O–C, alkoxy C–O, and carboxyl (C–O), respectively. That indicates that the GO surface is rich in

oxygen-containing functional groups. The principal peak at 1589 cm−1 corresponds to C=O in the COOH unit of GO. These firm peaks of stretching vibration of oxygen-containing functional

groups indicate the presence of many oxygen-containing functional groups on the surface of GO11,34,35. In contrast, for the CMC-GA-GO102 Composite, the characteristic C=O band of GO is

visible but not readily apparent, indicating the successful incorporation of GO. This peak's lack of visibility could be attributed to its low GO concentration36. Pure CMCNa bands at

1583 cm−1 (_vas_COO) and 1412 cm−1 (_vs_COO) corresponds to the antisymmetric and symmetric stretching of carboxylate groups, respectively, and the O–H stretching band appeared at 3244 cm−1.

The CH stretching frequency is 2920 cm−1. At 1319 cm−1, skeletal vibrations are also observed. The bending frequency of CC is 1019 cm−137,38. CMC-GA and CMC-GA-GO102 have comparable

characteristic peaks in their FT-IR spectra. The OH band was stretched at 3275 and 3362 cm−1, and the CH band at 2916 and 2929 cm−1 for CMC-GA and CMC-GA-GO102, respectively37.On the

spectrum of CMC-GA, two distinct peaks are observed at 3275 and 1022 cm−1, corresponding to –OH and C–O–C stretching vibrations, respectively. Despite these two peaks in the CMC-GA-GO102

composite, a clear red shift of the –OH peak from 3275 to 3362 cm−1 can be observed due to the presence of GO in the CMC-GA matrix. It indicates a robust hydrogen bonding interaction between

CMC and GO19. The characteristic band of C=O of GO cannot be observed in CMC or CMC-GA. However, after incorporating GO into the CMC-GA-GO102 composite, the absorption band at 1719 cm−1 can

still be observed (Fig. 1), indicating that the CMCNa cross-linking was successful. Moreover, at approximately 1636 cm−1, the carbonyl stretch of the carboxylic groups of GO overlapped with

the carboxylate groups of CMCNa, indicating a strong interaction between the carboxyl groups of GO and the hydroxyl groups of CMCNa39. The comparison of FTIR spectra reveals that the

CMC-GA-GO102 composite contains an abundance of hydrophilic groups, including hydroxyl, carboxyl, and epoxy groups, which all have excellent chemical activity and aid in the adsorption of

cationic dye40. In addition, by combining CMC-GA-GO102 with the MB dye molecules, the FTIR- spectra will exhibit dye-specific peaks. After the adsorption processes of dye species, shifts,

disappearances, the emergence of new bands, and alterations in peaks were observed. The peak at 3362 cm−1 shifted to 3434 cm−1, the peak at 1636 cm−1 shifted to 1588 cm−1, the peak at 1319 

cm−1 shifted to 1391 cm−1, and the peak at 1268 cm−1 shifted to 1215 cm−1. After surface adsorption of MB dye, the intensity and location of peaks in the structure of CMC-GA-GO102

nanocomposite changed. It signifies a reaction between the adsorbent and the contaminant dye. In addition, after MB dye adsorption, novel bands at 3434 cm−1 were observed, which were

attributed to the presence of MB. After MB dye adsorption, the range and intensity of peaks in CMC-GA-GO102 nanocomposite change very little. These minute differences may indicate the

existence of physical mechanisms (such as van der Waals forces) between the structure of the adsorbent and the pigment molecules. The obtained data indicate that the CMC-GA-GO102 composite

successfully eliminated MB dye. The minor shifts in the OH group suggest that hydroxyl-hydrogen atoms participated in the hydrogen bonding interaction between the composite and the dye12,41.

In addition to ionic interactions between the -OH groups in the CMC-GA-GO102 structure, it is believed that numerous abrupt decreases are due to MB species, with the band shifting

indicating that these functional groups interact with the MB molecules42. RAMAN ANALYSIS Raman spectroscopy can provide valuable information regarding GO structure, especially structural

alterations in prepared samples. Figure 1B depicts the Raman spectra of GO, CMC-GA, and the CMC-GA-GO102 composite. GO's Raman spectrum displayed two distinct peaks at 1611 cm−1 and

1347 cm−1, corresponding to the well-known G and D bands43. The D band with sp3 carbon is caused by defects in graphene oxide and staging disorder, whereas the hexagonal pressure mode of

graphite causes the G band. The ratio of the G/D peaks within the GO spectrum corresponds to the ratio of the Sp2 hybridized carbon bonds crystalline defects (G-band) and functional groups

present (D-band); this value is typically between 0.8 and 1.2 and is also an excellent indicator of the oxygen content; the lower the ratio, the fewer functional groups are present. In

graphitic materials, the D-band to G-band intensity (ID/IG ratio) is commonly used to characterize the defect density. The greater the number of sp2 hybrid carbon atoms, which corresponds to

a higher order degree of GO44,45, the lower the ID/IG ratio. In this investigation, the ID/IG ratio of graphene oxide was determined to be 0.87. 0.92 was the ID/IG ratio of the CMC-GA-GO102

nanocomposite. CMC-GA-GO102 has a higher ID/IG ratio than GO, indicating that the nanocomposite comprises nanosheets of ordered carbon. Moreover, because CMC-GA-GO102 nanocomposites are

less dense than graphene oxide, the intensities of the two peaks in GO and CMC-GA-GO102 nanocomposites were diminished. Moreover, a higher ID/IG ratio of CMC-GA-GO102 in comparison to GO

suggested that some of the oxygenated functional groups of functionalized CMC-GA-GO102 were involved in network formation, resulting in a decrease in their concentration and an increase in

the value of ID/IG ratio19. CMC-GA-GO102's Raman spectrum displays the corresponding characteristic peaks, such as the soft peaks of C–C stretching at 1269 cm−1 and the C=C symmetric

stretching peak at 1424 cm−1. Due to interactions between GO and CMC-GA, the composite's Raman peaks undergo changes in intensity or position. The FT-Raman spectral bands of CMCNa and

hybrid materials are highly similar. The band at 2907 cm−1 is attributed to C–H stretching, the band at 1118 cm−1 to symmetric stretching of the C(1)–O–C(4) group and ring respiration, and

the band at 918 cm−1 to bending C(5)C(6)–H and HC(6)O. SEM ANALYSIS The surface morphology of an adsorbent is one of the most influential factors governing the adsorption process. Therefore,

the composite's surface morphology and constituents were analyzed using scanning electron microscopy. Figure 2 depicts SEM images of (GO, CMC, CMC-GA, and the CMC-GA-GO102 generated

composite sample) before and after dye adsorption. Figure 2 depicts GO sheets that resemble rounded pleats, a cloud, and a flat-surfaced sheet-like structure46,47. Conversely, CMC has a

fibrous, woven surface structure48,49. The hydrogel's surface was virtually smooth and contained few pores. The SEM results for CMC-GA hydrogel and CMC-GA-GO102 nanocomposite hydrogel

revealed a three-dimensional structure that is porous and interconnected. Moreover, the composite SEM image revealed a rough structure, severe creases, and a uniform distribution of GO in

the polymer matrices. In addition, the results demonstrated that adding GO and GA to the CMC chains increased the number and size of pores in the CMC-GA-GO102 structure. Consequently, it is

anticipated that the CMC-GA-GO102 nanocomposite will have a higher removal capacity of MB from aqueous liquids than the CMC-GA50,51,52,53. After MB dye adsorption, the composite surface

reflects no porous onto their surface. EDX ANALYSIS As demonstrated in Fig. 3, EDX-SEM analysis is conducted on GO, CMC, CMC-GA, CMC-GA-GO102, and CMC-GA-GO102-MB to determine the elemental

composition of the investigated materials and confirm dye adsorption by the investigated composites. Before and after the MB adsorption procedure, the EDX analysis of the CMC-GA-GO102

composite was evaluated. CMC comprises C, O, and Na, as confirmed by Fig. 3A (elementary composition). The elemental analysis of GO reveals high concentrations of C and O, indicating that

the synthesized GO is of good purity, while other three beaks at 2.3 keV, 3.4 keV, and finally 5.8 keV referred to remaining residues of S from sulfuric acid, K, and Mn from potassium

permanganate used in the preparation method (Fig. 3B). Prior to the addition of GO, as shown in Fig. 3C, the atomic percentages of O, C, and Na in CMC-GA were 34.39%, 51.01%, and 14.60%,

respectively. When GO is incorporated into the CMC-GA, the atomic percentages of O, C, and Na are observed to be 56.48%, 30.78%, and 12.78%, respectively in Fig. 3D. The decrease in carbon

and sodium content and the increase in oxygen content indicate that GO incorporation has altered the chemical composition to include more oxide. However, the three beaks at 2.3 keV, 3.4 keV,

and finally 5.8 keV referred to remaining residues of S from sulfuric acid, K, and Mn from potassium permanganate used in the preparation of GO (Fig. 3B) still show up with lower intensity.

As shown in Fig. 3E, the CMC-GA-GO102-MB contains carbon, oxygen, nitrogen, sulfur, and chlorine after MB dye adsorption by CMC-GA-GO102, as well as a decrease in Na and O content, which

may refer to the adsorbed dye. TGA ANALYSIS Thermogravimetric analysis is an effective method for determining the temperature of weight loss, the rate of weight loss, and the weight of the

sample after weight loss. The TGA analysis of CMC, GO, CMC-GA, CMC-GA-GO102, and CMC-GA-GO102-MB is depicted in Fig. 4. On the TGA curves, as depicted in Fig. 4, the weight loss of the

samples could be broken down into several stages. The weight loss below 100 °C was due to water evaporation of the samples in the first step. In contrast, the successive weight loss between

200 and 400 °C could be attributed to the thermal decomposition of the samples. After the heating procedure, the TGA curve of CMC began to decrease gradually, and some functional groups

degraded. The curve was then progressively maintained at the same level from 70 to 240 °C, after which it dropped sharply to lose approximately 50% of its weight at 320 °C, leaving a 40%

residual weight54. In contrast, the TGA curve of GO was significantly thermally unstable, with over 55% of its weight loss occurring below 150 °C. GO was decomposed in four stages: moisture

evaporation at 39–96 °C, dehydration of adsorbed water at 96–152 °C, pyrolysis of O-rich functional groups –OH and C–O–C at 152–271 °C, and –COOH decomposition at 271–379 °C. At 800 °C, GO

loses approximately 80% of its mass55. It was also discovered that combining CMC and GO in a composite improved both, indicating that GO and CMC nanoparticles interact strongly. The

CMC-GA-GO102 curve began to decrease at 120 °C and then exhibited a modest change in slope until 350 °C, indicating that the degradation process of the complex composites was complete. In

addition, the residual content of CMC-GA-GO102 was 27%, the residual value of CMC was 16%, and the residual amount of GOs was 7%, proving that CMC was effectively modified onto the surfaces

of CMC-GA-GO10256. As depicted in Fig. 4, the thermal stability of CMC-GA-GO102 following adsorption of the MB dye species was approximately 60%. This phenomenon may be explained by the fact

that the adsorption process consumes various function groups, thereby weakening the electrostatic attraction between the precursors of the beads57. EFFECT OF THE BIOCOMPOSITES GO:CMC

COMPOSITION ON THE DYE REMOVAL Different amounts of GO were physically mixed with CMC solution, chemically crosslinked with GA, and then freeze-dried to produce CMC-GA-GOx biocomposites with

a distinct porosity. The CMC-GA-GOx biocomposites (Table 1) were evaluated for their ability to remove MB dye under fixed adsorption and compared the dye removal percentages (%) with the

CMC-GA hydrogel-based adsorbent (without GO) to show the contribution of GO incorporation and the resulted synergetic effect (Fig. 5A). Figure 5A depicts the percentage of MB dye removed by

the CMC-GA-GOx biocomposites, which is generally more significant than the CMC-GA counterpart. On the other hand, the GO:CMC (W%) ratio has a distinct positive synergetic effect on the dye

removal percentage, with GO:CMC (20%) providing the best results. Further, an increase in the GO weight ratio in the biocomposites adsorbents reduces positive synergetic effect on the

percentage of dye removal until it reaches the minimum increment value of the CMC-GA-GOx adsorbent with a 50% GO:CMC weight ratio. The data presented in Fig. 5A indicate that the positive

synergetic effect on the dye removal percentage increment were found 56.66%, 81.8%, 57.6%, and 25% for the CMC-GA-GO101, CMC-GA-GO102, CMC-GA-GO103, CMC-GA-GO105, respectively. The

explanation of the positive synergetic effect of GO incorporation could be referred to one or more of the following; * a. The high surface area and consequently high number of adsorption

active sites of GO compared with CMC, * b. Improvement of the composite porosity, * c. Creating of driving force through the concentration gradient between the MB aqueous phase and the

adsorbent solid one, * d. Blocking of the pores with agglomerated GO particles. The compromise between the above mentioned factors leads to obtained results which the CMC-GA-GO102

biocomposite has the highest increment percentage of MB dye removal compared with its CMC-GA counterpart which was almost doubled. Increasing the incorporated GO above 20% leads to reducing

the composite porosity as a result of blocking the pores with the agglomerated GO particles which creates a diffusion barrier of the MB from the aqueous phase to the adsorbent solid phase.

Above all, the concentration gradient greatly reduced as a result of increased the GO adsorption active sites and consequently fast equilibrium was reached. Accordingly, the CMC-GA-GO102

biocomposite was utilized to study the adsorption processes' operational conditions and evaluate the kinetic, isotherm, and thermodynamic properties of the MB adsorption process. EFFECT

OF CONTACT TIME AND ADSORPTION KINETICS Figure 5B depicts the effect of contact duration on the adsorption of MB dye by CMC-GA and CMC-GA-GO102.CMC-GA-GO102 eliminated 98.3% of MB dye,

while CMC-GA eliminated 61.25%. The adsorption removal and adsorption capacities of CMC-GA-GO102 for MB dye increased significantly within the first 25 min. A large number of active sites on

the CMC-GA-GO102 sorbent surface were capable of producing significant removal activity. The adsorption rate decreases due to the gradual filling of the adsorption sites. There is

insufficient contact between CMC-GA-GO102 and MB dye species for the first 25 min, but equilibrium is progressively reached after sufficient contact. This behavior is a result of the dye

molecules occupying the active sites and the adsorbent appearing saturated with the pollutant33, on the one hand, and the concentration gradient between the nano-biocomposite adsorbent solid

phase and the MB dye solution phase, which is primarily responsible for facilitating the transfer of the MB molecules from the solution to the adsorbent phase, decreasing over time until

equilibrium is reached, on the other hand. The equilibrium adsorption capacity was determined to be 73.73 mg/g. Kinetic studies for the adsorption of various pollutants, such as synthetic

dyes and heavy metal ions, are essential because they provide information on the time required to reach adsorption equilibrium, the rate of adsorption, and the concentration of adsorbate in

each phase after equilibrium has been reached58. To better comprehend the adsorption of MB dye onto CMC-GA-GO102 composite, the kinetic behavior was studied using Pseudo-first order (PFO)

and Pseudo-second order (PSO) as well as Intra-particle diffusion (IPD) kinetics models, which can be expressed as follows. The linear equation for the model of pseudo-first order is36;

$$\mathrm{ln}({q}_{e}-{q}_{t})=\mathrm{ln}{q}_{e}-{K}_{1}t$$ (3) where qe is the adsorption amount of dye in mg/g at equilibrium, qt (mg/g) is the Amount of MB dye adsorbed at time t and K1

(min−1) is the first order kinetic model’s rate constant. Table 1 summaries the values of K1, qe, and the correlation coefficient (R2) calculated from linear plots of

\(\mathrm{ln}(\mathrm{qe}-\mathrm{qt})\) versus t (Fig. 5C). The linear equation of the PSO model is59; $$\frac{t}{{q}_{t}}=\frac{1}{{k}_{2}{{q}_{e}^{2}}}+\frac{t}{{q}_{e}}$$ (4) K2 is the

rate constant of pseudo second-order kinetic model's adsorption (Fig. 5D). The linear equation for Intra-partical diffusion model is60; $$qt={k}_{p}{t}^{0.5}+c$$ (5) Kp is the rate

constant of the intra-particle diffusion kinetic model's (mg g−1/min) and it’s value can be found from the slope of qt versus t0.5 and C (mg g−1) is the intercept gives an indication of

the boundary-layer thickness (Fig. 5E). The parameters calculated from the slope and intercept of the linear plots of the Pseudo-First order, Pseudo-Second order, and Intra-particle

diffusion models are shown in Fig. 5C–E and tabulated in Table 2. Table 2 demonstrates that R2 of the Pseudo-second order model (R2 = 0.998) is greater than R2 of the Pseudo-First order

model (R2 = 0.942) for MB dye. Moreover, the calculated equilibrium capacity values (qe-cal = 76.92 mg/g) form the Pseudo-second order were found to be more closer to the corresponding

experimental values (qe-exp = 73.73) than those of Pseudo-First order model (qe-cal = 48.42 mg/g), indicating that the Pseudo-second order kinetic model can be well explain the kinetic of

the adsorption of MB dye onto the surface of CMC-GA-GO102 composite. The three-stage adsorption of MB dye on the surface of CMC-GA-GO102 composite was disclosed by plotting qt versus t0.5

(Fig. 5E). The first stage may be attributed to the diffusion of MB molecules from the bulk to the exterior surface of the CMC-GA-GO102 composite. The second stage consists of the MB dye

molecules' delayed diffusion. In the final stage, equilibrium is declared to have been attained. The linear plot of the intra-particle model (Table 2) revealed that the straight line

has nonzero intercept values, indicating that the adsorption of MB dye on CMC-GA-GO102 is likely to be complex and involve both film diffusion (boundary layer diffusion) and intra-particle

diffusion61. EFFECT OF INITIAL DYE CONCENTRATION AND ADSORPTION ISOTHERMS The eradication of dye is highly dependent on the initial concentration of dye. The effect of initial dye

concentration is determined by the direct relationship between the number of dye molecules in the solution and the available number of active sites on an adsorbent. Figure 5F depicts the

effect of initial dye concentrations (10–150 mg/L) on the adsorption percentages (%R) of MB dye from aqueous solution onto CMC-GA-GO102 nanocomposite was investigated. At the same time, all

other parameters were held constant. Figure 5F demonstrates that the adsorption percentage of MB dye onto CMC-GA-GO102 decreases as the initial concentration of MB dye increases at 25 min of

adsorption time. This effect is because the adsorbent had many active sites for the adsorption of the dye species at low initial dye concentrations. When the dye concentration was

increased, these vacant sites became saturated with MB dye species and lost their ability to absorb more dye molecules62,63,64. Consequently, as dye concentrations increase, adsorption

efficiency decreases65. Two adsorption isotherm models (Langmuir and Freundlich) were used to investigate the adsorption performance of the CMC-GA-GO102 composite and the interactions with

the MB dye molecules66. The Langmuir model assumes that a single layer of adsorption forms a homogeneous surface to explain the adsorption of MB dye on the surface of CMC-GA-GO102 based on

the correlation coefficient (R2 = 0.973), which indicates that the adsorption process occurs on a homogeneous active site as a monolayer; Fig. 5G. Its equation is given in67.

$$\frac{{c}_{e}}{{q}_{e}}=\frac{1}{{k}_{l}{q}_{m}}+\frac{{c}_{e}}{{q}_{m}}$$ (6) where qe (mg/g) is the amount of MB dye adsorbed onto the surface of the CMC-GA-GO102 composite at

equilibrium. Ce (mg L−1) is the MB equilibrium concentration. qm (mg/g) represents the maximum adsorption capacity of MB dye onto the adsorbent surface and KL (L/mg) represents the Langmuir

constant. The slope and intercept of the Ce/qe against Ce plot were used to calculate the values of qm and KL. In contrast, the Freundlich model proposes the existence of a heterogeneous

adsorbent surface68 is represented by the following equation: $$\mathrm{ln}{q}_{e}= {k}_{f}+\frac{1}{n}\mathrm{ ln}{c}_{e}$$ (7) kF (mg/g) and n represent Freundlich constants which describe

adsorption capacity and strength, respectively, and can be obtained from the intercept and slope of plotting ln qe with ln Ce; Fig. 5H. Furthermore, the 1/n values for MB dye is 0.149,

indicating that the procedure is not conducive to adsorption69. The related parameters calculated from the adsorption isotherm of MB dye species adsorption by CMC-GA-GO102 are listed in

Table 3. R2 = 0.973 for MB indicates that the adsorption of MB dye onto the CMC-GA-GO102 composite surface is homogeneous, as predicted by the Langmuir model. However, MB's Freundlich

isotherm determination coefficient (R2) was 0.591. The determination coefficient (R2) of the Langmuir isotherm was much higher than that of the Freundlich isotherm, the theoretical qm

obtained from the Langmuir model was found to be 76.92 mg/g for MB matching the experimentally determined value (73.73 mg/g), while the theoretical qm obtained from the Freundlich isotherm

was found to be 56.347689 mg/g. The obtained results confirmed the complete homogenization of the GO nanoparticles in the CMC-GA solution. EFFECT OF ADSORPTION TEMPERATURE AND THERMODYNAMICS

Figure 5I illustrates the effect of dye solution temperature in the range of (25–65 °C) on the adsorption efficiency of MB onto CMC-GA-GO102 adsorbent with all other factors held constant.

When the aqueous solution temperature increased from 25 °C to 65 °C, the MB dye adsorption efficiency decreased from 98.3 to 66.5%, indicating that MB dye adsorption onto CMC GA-GO102

composite is an exothermic process. Therefore, to conserve energy, we chose 25 °C for the subsequent series of investigations70. The decrease in adsorption efficiency can be explained by an

increase in the propensity for the adsorbed dye to dissociate from the solid surface and leach into the liquid, the contraction of active sites at high working temperatures, and a decrease

in the effective concentration gradient driving force12. That is likely because the thermal motion of the MB molecules accelerated at high temperatures, resulting in a rapid equilibrium

between adsorption and desorption36. Therefore, thermodynamic studies were used to investigate the thermal changes and spontaneous ability of MB dye's adsorption processes and reactions

system onto CMC-GA-GO102 composite (Fig. 5J). The standard Gibbs free energy change (G), the standard enthalpy change (H), and the standard entropy change (S) were measured as thermodynamic

parameters using Van't Hoff equations71,72 to learn more about the nature of this process. $$\mathrm{ln}\frac{{q}_{e}}{{c}_{e}}=\frac{\Delta S}{R}-\frac{\Delta H}{RT}$$ (8)

$$K=\frac{{q}_{e}}{{c}_{e} }$$ (9) $$\Delta G=-\mathrm{RTln}K $$ (10) _K_ is the thermodynamic equilibrium constant, T (K) is the temperature, and R (8.314 J mol−1 K−1) is the general gas

constant. H/R is calculated according to Eq. (8) by plotting ln K versus 1/T. The y-axis intercept is used to calculate S/R. Table 4 displays the parameters for the adsorption of MB dye onto

CMC-GA-GO102 composite derived from thermodynamic calculations measured by the linear relation of van't Hoff equation at various temperatures. The decreasing K values with increasing

temperature and the negative H° value indicate that MB adsorption onto the CMC-GA-GO102 composite is exothermic. In addition, the entropy (S) change was negative (-187.56 J/mol K),

indicating that the process is more practicable at lower temperatures. In addition, the decrease in negative G° values with increasing temperature indicates that the process is more

spontaneous at lower temperatures. EFFECT OF ADSORPTION PH The treatment pH is one of the most influential factors on adsorbent capacity in wastewater treatment, as it substantially affects

the adsorbent surface charge, dissociation of the functional groups of the adsorbents, and the degree of ionization of the adsorptive species consequently, removal effectiveness. Therefore,

pH is a factor that controls adsorption. The effect of solution pH on CMC-GA-GO102 removal efficiency was studied by modulating the pH of MB dye solution from 2 (extremely acidic) to 11

(extremely alkaline) while maintaining all other parameters constant. The synthesized anionic CMC-GA-GO102 nanocomposites, including the hydroxyl and carboxyl functional groups, were

affected by the pH of the dye solution. Figure 5K illustrates how pH affects the adsorption of MB dye species. It was evident that the removal (%) for MB increased from 81 to 98.3% as the pH

rose from 2 to 11. The lower efficiency at low pH values (strongly acidic) was due to the carboxyl and hydroxyl functional groups are mostly in non-ionized (–OH, –COOH) form and a low

interaction can occur between the cationic dyes and these groups6; also the H+ ions existing in the solution compete with the cationic MB for negative sites of the adsorbents like carboxylic

acid. Thus, it is difficult for MB molecules to diffuse on the adsorbent surface73; hence, the dye removal percentage (%) is reduced. The adsorption capacity increased linearly with the

increase of pH value, up to pH 7. At this pH value, the carboxyl and hydroxyl functional groups of the CMC-GA-GO102 nanocomposites dissociate. Therefore, these groups are present in –O− and

–COO− form in the CMC-GA-GO102 nanocomposites, and strong electrostatic interactions could occur between the positive site of MB and the negative site of the CMC-GA-GO102 adsorbent.

Likewise, at pH values higher than 7, up to pH 11, there was a lower rate of increase in the adsorption that could be related to the existence of a large amount of Na+in the MB solution

medium reduced interactions between MB and the anionic functional group of CMC-GA-GO102 adsorbent73,74. EFFECT OF THE CMC-GA-GO102 DOSAGE Figure 5L depicts the percentages of dye adsorption

(R%) at different CMC-GA-GO102 dosage (mg). The results demonstrated that, at constant MB dye concentration, the adsorption percentage of MB increases from 60.5 to 99.8% with increasing

CMC-GA-GO102 adsorbent dose in the range of 0.005–0.05 g, which directly increased the number of active sites, thereby increasing the adsorption efficiency19,75,76. However, the dye removal

percentage is nearly constant when mixing 0.02 g of CMC-GA-GO102 composite, so that the current investigation will use 0.02 g of CMC-GA-GO102 adsorbent. EFFECT OF NACL DOSE Under optimal

conditions, the effect of NaCl on the removal percentages of MB dye using CMC-GA-GO102 nanocomposite was evaluated and illustrated in Fig. 5M. As shown in the figure, varying concentrations

of sodium chloride in the range of 0.1 to 0.5 g were used to determine the influence of salt concentration on the %R of the investigated dye on CMC-GA-GO102. The removal percentage of MB dye

decreased swiftly after the addition of NaCl. Electrostatic filtration effects are the primary cause of this effect. In other terms, Na+ ions and cationic MB molecules compete for anionic

binding sites on the CMC-GA-GO102 adsorbent. As a result, their absorption is diminished. By enhancing the ionic strength of the aqueous medium, the presence of NaCl shields the active

surface sites. Positively charged Na ions in aqueous dye solutions may decrease the negative charge of active sites on the adsorbent surface, thereby diminishing the electrostatic attraction

forces between dye molecules and negatively charged active sites. Moreover, the presence of NaCl in the dye solution phase creates an osmosis difference that causes water molecules to

migrate from the swollen CMC-GA-GO102 adsorbent to the MB liquid phase, resulting in de-swelling of the CMC-GA-GO102 adsorbent and a diffusion barrier against the MB molecules entering the

adsorbent's interior porous structure. By illustration, the system containing no added salt had an MB adsorption percentage of approximately 98.3%, whereas the system containing 0.5 g

NaCl had a value of approximately 49.6%21,59. REUSABILITY The main goal of regeneration process is to reuse the adsorbent materials for many times as much as possible. Cycles of adsorption

and desorption have been tried under the same conditions using 3% NaCl solution for the CMC-GA-GO102-MB regeneration (Fig. 5N). It is clear from the figure that gradual decreases of the MB

dye removal percentage has been observed with successive adsorption–desorption cycles. However, the MB dye removal percentage reaches 86% after ten adsorption–desorption successive cycles.

That result indicates that the CMC-GA-GO102 adsorbent lost only 14% of its adsorption efficiency and consequently proved the capability of reusing the developed CMC-GA-GO102 adsorbent.

COMPARATIVE STUDY Table 5 presents a comparative analysis of MB removal by chemically modified polyacrylonitrile. Additionally, additional absorbents are included. It is evident from the

table that Salisu et al.77 eliminated methylene blue (MB) dye with alginate graft-polyacrylonitrile beads. They discovered that the maximal monolayer coverage of Langmuir was 3.51 mg/g.

Kiani et al.78 developed polyacrylonitrile (PAN) and monoethanolamine-based chelating resins to remove methylene blue from an aqueous solution. The maximal adsorption capacity was determined

to be 52.3 mg/g. Abu-Saied et al. The Langmuir adsorption capacity (Qo) was determined to be 54 mg/g. Natural adsorbents, such as H. cannabinus-g-PAA and H. cannabinus-g-PAA/PAAM, have a

limited adsorption capacity (7.0 mg/g)80, regardless of grafting with functional polymers. The adsorption capacity of activated lignin-chitosan composites and brown macroalga is moderately

moderate (35–36 mg/g)81,82. The adsorption capacity of inorganic adsorbents such as MOF is moderately high (326 mg/g)83. The maximum adsorption capacity of nano-hydroxamate polyacrylonitrile

(HPAN) particles is 8.34 (mg/g)84. The CMC-GA-GO102 adsorbent developed in the present study has a monolayer adsorption capacity of 106.95 mg/g. CONCLUSION Glutaraldehyde crosslinked sodium

carboxymethyl cellulose (CMC-GA) hydrogel, and its nanographene oxide composite (CMC-GA-GOx) were used to develop an effective carboxymethyl cellulose-graphene oxide biobased composites

adsorbent for the removal of methylene blue (MB) cationic dye contaminate from industrial wastewater. The optimal GO weight percentage was discovered to be 20%; CMC-GA-GO102. Several

variables affecting the elimination of MB dye have been investigated. After 25 min of adsorption, 98% of the 30 ppm MB was removed, indicating that the equilibrium was reached rapidly. The

optimal pH range for adsorption was between 2.0 and 5.0, where the removal (%) increased from 81.0 to 93.0% for MB, whereas the removal percentage reached equilibrium at 98.0% with a pH of

11. When the aqueous solution temperature increased from 25 to 65 °C, the MB dye adsorption efficiency decreased from 98.3 to 66.5%, indicating that MB dye adsorption onto CMC GA-GO102

composite is an exothermic process. Regarding initial MB concentration, the adsorption %R of MB dye onto CMC-GA-GO102 decreased almost linearly from 30 to 150 ppm at 25 min of adsorption

time. The highest MB removal percentages were obtained within a concentration range of 10 to 30 ppm. At constant MB dye concentration, the adsorption percentage of MB increases from 60.5 to

98.0% with increasing CMC-GA-GO102 adsorbent dose in the range of 0.005–0.02 g, where equilibrium was nearly attained. Increasing the adsorbent dose to 0.05 g resulted in a modest increase

in the MB removal percentage. Any concentration of NaCl harms the MB removal percentage. The experimental data of the adsorption process were more consistent with the Langmuir isotherm, in

which the maximal monolayer adsorption capacity was determined to be 76.92 mg/g. The adsorption process followed the kinetic model of pseudo-second order. The removal of MB was exothermic

and spontaneous from a thermodynamic standpoint. In addition, thermodynamic results demonstrated that adsorption operates most effectively at low temperatures. These results suggest that the

CMC-GA-GO102 composites could be a cost-effective adsorbent for removing organic cationic dyes from industrial wastewater. Cycles of adsorption and desorption have been tried under the same

conditions using 3% NaCl solution for the CMC-GA-GO102-MB regeneration. The MB dye removal percentage reaches 86% after ten adsorption–desorption successive cycles. That result indicates

that the CMC-GA-GO102 adsorbent lost only 14% of its adsorption efficiency and consequently proved the capability of reusing the developed CMC-GA-GO102 adsorbent. A comparative analysis of

the removal of MB by various other adsorbents revealed that the CMC-GA-GO102 adsorbent developed in this study has a moderately high monolayer adsorption capacity. In addition, the

CMC-GA-GO102 composite was characterized using FTIR, RAMAN, TGA, SEM, and EDX analysis instruments. As a result of the interaction between the CMC-GA-GO102 adsorbent and the MB dye

molecules, the FTIR spectrum displays peaks corresponding to the dye species. After the adsorption processes of dye species, observations of shifts, disappearances, the emergence of new

bands, and alterations in peaks were observed. At 1215 cm−1, 879 cm−1, and 832 cm−1, distinctive peaks appeared for C–N stretching, aromatic C–H bond, and out-of-plane bending, respectively.

The peak at 3362 cm−1 became 3434 cm−1, the peak at 1636 cm−1 became 1588 cm−1, the peak at 1319 cm−1 became 1391 cm−1, and the peak at 1268 cm−1 became 1215 cm−1. After surface adsorption

of MB dye, the intensity and location of peaks in the structure of CMC-GA-GO102 nanocomposite changed. It signifies a reaction between the adsorbent and the contaminant dye. In addition, the

EDX analysis of the CMC-GA-GO102-MB reveals that it contains carbon, oxygen, nitrogen, sulfur, and chlorine. Furthermore, the Na and O content of the CMC-GA-GO102 will decrease, proving the

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provided by The Science, Technology & Innovation Funding Authority (STDF) in cooperation with The Egyptian Knowledge Bank (EKB). AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Department

of Chemistry, Faculty of Science, Alexandria University, P.O.Box 426, Alexandria, 21321, Egypt Eman N. Mohamed & Ali A. El-Bardan * Advanced Technology and New Materials Research

Institute (ATNMRI), City of Scientific Research and Technological Applications (SRTA-City), New Borg Al Arab, 21934, Alexandria, Egypt Ahmed I. Abd-Elhamid & Hesham M. A. Soliman *

Polymer Materials Research Department, Advanced Technology and New Materials Research Institute (ATNMRI), City of Scientific Research and Technological Applications (SRTA-City), New Borg Al

Arab, 21934, Alexandria, Egypt Mohamed S. Mohy-Eldin Authors * Eman N. Mohamed View author publications You can also search for this author inPubMed Google Scholar * Ahmed I. Abd-Elhamid

View author publications You can also search for this author inPubMed Google Scholar * Ali A. El-Bardan View author publications You can also search for this author inPubMed Google Scholar *

Hesham M. A. Soliman View author publications You can also search for this author inPubMed Google Scholar * Mohamed S. Mohy-Eldin View author publications You can also search for this

author inPubMed Google Scholar CONTRIBUTIONS Prof. Dr. A.A.E. and Prof. Dr. H.M.A.S. has proposed the point of research, and revises the final version of the manuscript. Assoc. Prof. Dr.

A.I.A. designs the experimental work, follows the executive of the work, and supervises the writing of the first draft of the manuscript. Chem. E.N.M. has executed the experiments, drawing

the figures and tabulating the data, writes the first draft of the manuscript, and submitted the manuscript for publication. Prof. Dr. M.S.M. respond to the reviewers’ comments, makes the

required corrections, added further detailed discussions, and revised the entire manuscript language through the following contributions: (A) Declaring the novelty of the current work in the

introduction part as investigates the merging of different approaches for modifying carboxymethyl cellulose with GO to enhance its sorption of MB dye. These approaches include the

followings: (1) Chemical crosslinking of the CMC to create a three-dimensional porous structure with improved mechanical properties and surface area, (2) Physical crosslinking through the

free drying technique creates additional porosity and internal surface area, (3) It induces additional adsorption sites by mixing GO particles with additional surface area. (B) Improving the

discussion of the GO contribution in the properties of the developed CMC-GA-GOx composites through investigate the role of the CMC counterpart in the developed composite shown in Fig. 5A.

(C) Check the calculations of the kinetics, isotherms, and thermodynamics parameters and correct wherever needed in the redrawn figures and tables. (D) Improving the discussion of the

adsorption pH effect. (E) Discuss the reusability study. (F) Provided the adsorption conditions in Table 5. CORRESPONDING AUTHOR Correspondence to Eman N. Mohamed. ETHICS DECLARATIONS

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permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Mohamed, E.N., Abd-Elhamid, A.I., El-Bardan, A.A. _et al._ Development of carboxymethyl cellulose-graphene oxide biobased composite for the

removal of methylene blue cationic dye model contaminate from wastewater. _Sci Rep_ 13, 14265 (2023). https://doi.org/10.1038/s41598-023-41431-8 Download citation * Received: 02 June 2023 *

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