A study on water and dye sorption capacities of novel ternary acrylamide/sodium acrylate/PEG semi IPN hydrogels

Here, a novel ternary semi interpenetrating polymer networks (semi IPNs) have been synthesized. An effective role to develop mechanically strong polymeric materials has been through the preparation of interpenetrating polymer networks (IPNs). The highly swelling superabsorbent semi IPNs were prepared by introducing poly(ethylene glycol), (PEG) into an acrylamide/sodium acrylate, (AAm/SA) hydrogels. For swelling characterization, swelling experiments were performed in water at 25 °C, gravimetrically. Water uptake and dye sorption properties of AAm/SA hydrogels and AAm/SA/PEG semi IPNs were investigated as a function of chemical composition of the hydrogels. AAm/SA hydrogels and AAm/SA/PEG semi IPNs were used in experiments on sorption of water-soluble cationic dye such as “Janus Green B” (JGB). For sorption of JGB into AAm/SA hydrogels and AAm/SA/PEG semi IPNs were studied by batch sorption technique at 25 °C. For the analysis of sorption mechanism and for calculation of some binding parameters of JGB from aqueous solutions, some linearization methods such as Klotz, Scatchard, and Langmuir linearization methods have been used.     

Dye Sorption and Water Uptake Properties of Crosslinked Acrylamide/Sodium Methacrylate Copolymers and Semi-Interpenetrating Polymer Networks Composed of PEG

A series of novel semi-interpenetrating polymer networks hydrogels composed of poly(ethylene glycol) and random copolymer of acrylamide/sodium methacrylate were prepared by polymerization of aqueous solution of acrylamide, sodium methacrylate using ammonium persulphate/N,N,N′,N′-tetramethylethylenediamine as a redox-initiating pair in the presence of poly(ethylene glycol) and poly(ethylene glycol)diacrylate as crosslinker. Fourier Transform Infrared spectroscopy was used to identify the presence of different repeating units in the semi IPNs. Water uptake and dye-sorption properties of acrylamide/sodium methacrylate hydrogels and acrylamide/sodium methacrylate/poly(ethylene glycol) semi IPNs were investigated as a function of chemical composition of the hydrogels. Cationic dye, Janus Green B have been used in sorption studies as a model molecule. This study has given the quantitative information on the swelling and sorption characteristic of acrylamide/sodium methacrylate hydrogels and acrylamide/sodium methacrylate/poly(ethylene glycol) semi IPNs in many potential applications.     

Water and dye sorption studies of novel semi IPNs: Acrylamide/4‐styrenesulfonic acid sodium salt/peg hydrogels

In this study, it has been investigated that the incorporation of poly(ethylene glycol), (PEG) and 4‐styrenesulfonic acid sodium salt, (NaSS) into acrylamide, (AAm) hydrogel during free radical solution polymerization synthesis. Poly (ethylene glycol)dimethacrylate, (PEGDMA) was used as a multifunctional crosslinker in polymerization. The main purpose of this study was to combine both monomers and a polymer in a new polymeric system. Dye sorption properties of hydrogels and semi IPNs were investigated by using cationic dye such as Union Green B (Janus Green B, UGB). Swelling and sorption studies were carried out at 25°C. For structural characterization, FTIR analysis was made. The equilibrium percentage swelling (S_eq%) ranges are 660–1330% for AAm/NaSS hydrogels and 580–1310% for AAm/NaSS/PEG semi IPNs. To determine the sorption behaviors of cationic dye UGB, some sorption parameters such as sorption capacity (q), adsorption percentage (Ads%) and partition coefficient (K_d) of the hydrogels were investigated. Binding characterization has been studied by Langmuir linearization method. The sorption capacity values of the hydrogel systems were changed between 1.24 × 10^?4 and 4.05 × 10^?4 mol g^?1. The values of Ads% of the hydrogels were changed among 18?67%, and the values of K_d of the hydrogels were between 0.22 and 2.02. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

Preliminary swelling and dye sorption studies of acrylamide/4-styrenesulfonic acid sodium salt copolymers and semi-interpenetrating polymer networks composed of gelatin and/or PEG

Semi-IPN hydrogels based gelatin (GEL) and/or poly (ethylene glycol) (PEG) were prepared with acrylamide (AAm) and 4-styrenesulfonic acid sodium salt, (SSS) as a water adsorbent for cationic dye (methyl violet, MV) sorption. For this, chemically crosslinked copolymer of AAm/SSS copolymer with GEL and/or PEG were prepared by polymerization of aqueous solution of AAm and SSS using ammonium persulfate (APS)/N,N,N′,N′-tetramethylethylenediamine (TEMED) as redox initiating pair in presence of poly(ethylene glycol)diacrylate (PEGDA) as crosslinker. FT-IR analysis was used to identify the presence of different repeating units in the semi-IPNs. Surface morphology was characterized by scanning electron microscopy (SEM). Some swelling and diffusion characteristics were calculated for different semi-IPNs and hydrogels prepared under various formulations. Water uptake, and dye sorption properties of the crosslinked polymeric systems such as AAm/SSS, AAm/GEL/SSS, AAm/PEG/SSS and AAm/GEL/PEG/SSS hydrogel systems were investigated as a function of chemical composition of the hydrogels. MV have used in sorption studies.     

Swelling behavior of semi‐interpenetrating polymer network hydrogels composed of poly(vinyl alcohol) and poly(acrylamide‐co‐sodium methacrylate)

Interpenetrating polymer network (IPN) hydrogels based on poly(vinyl alcohol) (PVA) and poly(acrylamide‐co‐sodium methacrylate) poly(AAm‐co‐SMA) were prepared by the semi IPN method. These IPN hydrogels were prepared by polymerizing aqueous solution of acrylamide and sodium methacrylate, using ammonium persulphate/N,N,N¹,N¹‐tetramethylethylenediamine (APS/TMEDA) initiating system and N,N¹‐methylene‐bisacrylamide (MBA) as a crosslinker in the presence of a host polymer, poly(vinyl alcohol). The influence of reaction conditions, such as the concentration of PVA, sodium methacrylate, crosslinker, initiator, and reaction temperature, on the swelling behavior of these IPNs was investigated in detail. The results showed that the IPN hydrogels exhibited different swelling behavior as the reaction conditions varied. To verify the structural difference in the IPN hydrogels, scanning electron microscopy (SEM) was used to identify the morphological changes in the IPN as the concentration of crosslinker varied. In addition to MBA, two other crosslinkers were also employed in the preparation of IPNs to illustrate the difference in their swelling phenomena. The swelling kinetics, equilibrium water content, and water transport mechanism of all the IPN hydrogels were investigated. IPN hydrogels being ionic in nature, the swelling behavior was significantly affected by environmental conditions, such as temperature, ionic strength, and pH of the swelling medium. Further, their swelling behavior was also examined in different physiological bio‐fluids. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 302–314, 2005     

Water Sorption and Dye Uptake Studies of Highly Swollen AAm/AMPS Hydrogels and Semi-IPNs with PEG

A semi-interpenetrating network (semi-IPNs) hydrogel, composed of acrylamide (AAm) with 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) as co-monomer, with poly(ethylene glycol) (PEG) and two multifunctional cross-linkers such as 1,4-butanediol dimethacrylate (BDMA), and trimethylolpropane triacrylate (TMPTA) was prepared. AAm/AMPS hydrogels and AAm/AMPS/PEG semi-IPNs were synthesized by free radical solution polymerization. Swelling experiments were performed in water at 25°C, gravimetrically. For sorption of Toluidin Blue (Basic Blue 17, TB) into AAm/AMPS hydrogels and AAm/AMPS/PEG semi-IPNs was studied by batch sorption technique at 25°C. Dye removal capacity, removal effiency and partition coefficient of the hydrogels was investigated.     

A Novel Polymeric Adsorbent for Water and Dye Uptake: Acrylamide/Sodium Acrylate Copolymers and Semi-Interpenetrating Polymer Networks Composed of Gelatin and/or PVA

Gelatin (GEL) and poly (vinyl alcohol) (PVA)-based semi-interpenetrating polymer network (semi-IPN) hydrogels were prepared for cationic dye sorption. Chemically cross-linked copolymer of acrylamide/sodium acrylate (AAm/SA) with PVA and/or GEL were prepared by polymerization of aqueous solution of AAm, and SA using ammonium persulphate/N,N,N’,N’-tetramethylethylenediamine as redox initiating pair in presence of poly(ethylene glycol)diacrylate as cross-linker. FTIR analysis was used for structural characterization. Surface morphology was characterized by SEM. Methyl violet has been used in sorption studies. Water uptake, and dye sorption properties of the cross-linked polymeric systems were investigated as a function of chemical composition of the hydrogels.     

Swelling characterization of poly (acrylamide-<Emphasis Type="Italic">co</Emphasis>-<Emphasis Type="Italic">N</Emphasis>-vinylimidazole) hydrogels crosslinked by TMPTA and semi-IPN’s with PEG

In this study, a novel semi-interpenetrating network (semi-IPN’s) hydrogel, composed of acrylamide (AAm) with N-vinylimidazole (NVI) as comonomer, with poly (ethylene glycol)(PEG) and a multifunctional crosslinker such as trimethylolpropane triacrylate (TMPTA) was prepared. Highly swollen poly (AAm/NVI) hydrogels and semi-IPN’s were synthesized by free radical solution polymerization. Swelling experiments were performed in water at 25°C, gravimetrically. The influence of NVI and PEG content in hydrogels were examined. Poly (AAm/NVI) and poly (AAm/NVI/PEG) hydrogels showed large extents of swelling in aqueous media the swelling being highly dependent on the chemical composition of the hydrogels. Swelling ratio of poly (AAm/NVI) hydrogels and poly (AAm/NVI/PEG) hydrogels was shown 7.16–39.85. Diffusion behavior was investigated. Water diffusion into hydrogels was found to be non-Fickian in character. This study has given the quantitative information on the swelling characteristic of poly (AAm/NVI) hydrogel and semi-IPN’s as water absorbent in many potential applications.     

Swelling Characterization and Adsorptive Features of Acrylamide/Itaconic Acid Hydrogels and Semi-IPNs for Uranyl Ions

A novel semi-interpenetrating network (semi-IPNs) hydrogel, composed of acrylamide (AAm) with itaconic acid (ITA) as co-monomer, with poly (ethylene glycol)(PEG) and trimethylolpropane triacrylate (TMPTA) was prepared. Hydrogels and semi-IPNs were synthesized by free radical solution polymerization. Swelling experiments were performed in water and aqueous solutions of uranyl acetate. Diffusion behavior was investigated and their diffusion into hydrogels was found to be non-Fickian in character. Sorption of uranyl ion onto the polymeric system was studied by a batch sorption technique at 25°C. The sorption capacity, removal effiency and partition coefficient of the hydrogels were investigated.     

Poly[(N‐isopropylacrylamide)‐co‐(itaconic acid)] hydrogels with poly(ethylene glycol)

The aim of the work reported here was to investigate temperature‐ and pH‐sensitive hydrogels of N‐isopropylacrylamide (NIPAM) and itaconic acid (IA) and their semi‐interpenetrating polymer networks (semi‐IPNs) with varying contents of poly(ethylene glycol) (PEG). The stimuli responsiveness, swelling behaviour and mechanical properties of the hydrogels and semi‐IPNs were studied in order to investigate the effect of various amounts of PEG. Pulsed‐gradient spin‐echo NMR experiments were carried out to investigate the diffusion process. The pH sensitivity increased with an increasing amount of PEG in the semi‐IPNs, while the overall rate of water uptake was diffusion‐controlled (n < 0.5). For certain PEG contents (5 and 10 wt%), the semi‐IPNs exhibited better mechanical properties than the poly(NIPAM‐co‐IA) copolymer. The calculated values of the self‐diffusion coefficients of water indicated facilitated diffusion of water through the system with increased amounts of PEG, while the self‐diffusion coefficients of a model compound, metoprolol tartrate, showed no significant dependence on the amount of PEG. According to the results obtained and compared to results reported in the literature, the investigated semi‐IPNs may have potential applications in the controlled release of macromolecular active agents such as proteins and peptides. Copyright © 2009 Society of Chemical Industry     

Swelling behavior and diffusion studies of high‐water‐retaining acrylamide/potassium methacrylate hydrogels

Poly(acrylamide‐co‐potassium methacrylate) hydrogels were prepared by free‐radical simultaneous polymerization with aqueous solutions of acrylamide (AAm) and potassium methacrylate (KMA) with a redox initiator. The copolymerization was performed with eight different compositions of KMA at a fixed concentration of oil‐soluble crosslinkers, including 1,4‐butanediol diacrylate and ethylene glycol dimethacrylate (EGDMA). For every composition of AAm/KMA copolymer, the percentage swelling, swelling equilibrium, and diffusion characteristics were investigated. The copolymers were further studied for deswelling properties. The power law relationships of the hydrogels were evaluated for variation in terms of saline concentration. The AAm/KMA copolymers were confirmed by IR spectroscopy. Thermal studies of hydrogels were performed with differential scanning calorimetry and thermogravimetric analysis. EGDMA was found to be a better crosslinker for obtaining higher swelling and deswelling properties for the AAm/KMA hydrogels. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1153–1164, 2005     

Preparation and swelling behaviors of porous hemicellulose‐g‐polyacrylamide hydrogels

Novel porous hydrogels were successfully synthesized from hemicelluloses (HCs) and acrylamide (Am) with poly(ethylene glycol) (PEG) as the porogen. The prepared hydrogels were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, and scanning electron microscopy (SEM). The results show that the used PEG was not involved in the formation process of the hydrogels, and the HC‐g‐polyacrylamide hydrogels displayed a higher thermal stability than the hemicellulosic polymer. SEM analysis confirmed that the prepared hydrogels had porous structures. The effects of the Am/HC ratio, the amount and molecular weight of PEG and the amount of the crosslinker N,N‐methylene bisacrylamide on the swelling ratio of the prepared hydrogels were investigated in detail. The experimental data were fitted with the exponential heuristic equation and the Schott second‐order dynamic equation. The diffusion of water molecules into the hydrogel network was found to be non‐Fickian in behavior, and the swelling kinetics could be described by the Schott second‐order dynamic equation. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Poly(2‐hydroxyethyl methacrylate) hydrogel: from a brittle material to a nanofilled semi‐interpenetrating polymer network with potential application in wound dressings

In this work we report the photopolymerization of poly(2‐hydroxyethyl methacrylate) (PHEMA) together with a hydrophilic chitosan derivate (carboxymethyl‐chitosan) to yield a semi‐interpenetrating polymer network (semi‐IPN) that was filled with poly(N‐vinylcaprolactam)/poly(ethylene glycol methacrylate) core–shell nanogels in order to enhance the mechanical properties of the resulting hydrogels. The mechanical properties of the nanofilled semi‐IPNs were found to be more suitable for wound dressing applications than the PHEMA hydrogel as described by dynamic mechanical analysis in dry form and submerged in water. This was evidenced by a higher Young's modulus and higher elongation at break in the semi‐IPNs compared to blank PHEMA hydrogels. Furthermore, when the hydrogels were filled with nanogels, there was an elongation at break similar to that of skin with only a slightly lower Young's modulus. © 2019 Society of Chemical Industry     

Blood protein adsorption onto macroporous semi‐interpenetrating polymer networks (IPNs) of poly(ethylene glycol) (PEG) and poly(2‐hydroxyethyl methacrylate) (PHEMA) and assessment of in vitro blood compatibility

This work reports a study of the adsorption of fibrinogen (Fgn) onto the surface of semi‐interpenetrating polymer networks (IPNs) of poly(ethylene glycol) (PEG) and poly(2‐hydroxyethyl methacrylate) (PHEMA). The semi‐IPNs were prepared by polymerizing 2‐hydroxyethyl methacrylate with a redox system and in the presence of PEG and crosslinker ethyleneglycol dimethacrylate. The proposed spongy IPNs were characterized by Fourier transform infrared and environmental scanning electron microscopy methods, and network structural parameters, such as molecular weight between crosslinks and crosslink density, were calculated using swelling measurements. The adsorption of Fgn was carried out onto the spongy IPNs and kinetic constants of the adsorption process as well as isotherm constants were evaluated. The adsorption process was also studied under varying pH, ionic strengths, and chemical architecture of the IPNs. The anti‐thrombogenic behaviour of the polymer matrices was judged using in vitro tests. Copyright © 2006 Society of Chemical Industry     

A New Sorbent Chemically Cross-linked Highly Swollen Copolymeric Hydrogels for Dye Uptake

Water uptake and the sorption properties of polyelectrolyte hydrogels made by the polymerization of acrylamide (AAm) with maleic acid (MA) were investigated as a function of composition to find materials with swelling and dye sorption properties. Highly swollen acrylamide/maleic acid (AAm/MA) hydrogels were prepared by free radical solution polymerization in aqueous solutions of AAm with MA as comonomer and two multifunctional cross-linkers such as trimethylolpropane triacrylate (TMPTA) and 1,4-butanediol dimethacrylate (BDMA). Swelling experiments were performed in water at 25°C, gravimetrically. Chemically cross-linked AAm/MA hydrogels were used in experiments on sorption of water-soluble monovalent cationic dyes such as “Nil blue” (NB) and “Methyl violet (MV)”. Weight-swelling ratio values of AAm/MA hydrogels were calculated range 8.88–61.46. Some swelling kinetic parameters were found. Diffusion behavior of water and water sorption rate constant were investigated. Water diffusion into hydrogels was found to be non-Fickian in character. For sorption of cationic dyes, NB and MV into AAm/MA hydrogels were studied by batch sorption technique at 25°C. AAm/MA hydrogels in the dye solutions showed coloration. However, the AAm hydrogel did not show sorption of any dye from solution. The amount of the dye sorbed per unit mass of AAm/MA hydrogels was investigated.     

Synthesis and characterization of acrylamide and 2‐hydroxylpropyl methacrylate hydrogels for specialty applications

To modify acrylamide (AAm) hydrogels for specialty applications, it was copolymerized with 2‐Hydroxypropyl methacrylate (HPMA) in different molar ratio at 25°C in 1:1 water–acetone solvent system, using ammonium persulphate (APS) and N,N,N,N‐tetramethyl ethylene diamine (TEMED) initiator–accelerator system. Two series of hydrogels were thus prepared using two different crosslinkers—ethylene glycol dimethacrylate (EGDMA) and N,N‐methylene bisacrylamide (N,N‐MBAAm). To affect property profile of the hydrogels, concentration of HPMA was varied over a range of five concentrations from 3.5 to 28 mM. Hydrogels were further functionalized by partial hydrolysis with NaOH and Hofmann amide degradation reaction. FTIR, Nitrogen analysis, and SEM were used to establish monomer reactivity and structure relationship of the hydrogels. Metal ion uptake was studied as a function of various structural aspects of the hydrogels. Water uptake behavior of the hydrogels was studied at constant time, temperature, and pH, both pre and post metal loading. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 99: 3040–3049, 2006     

Behaviors of polyelectrolyte AAm/AMPS/bentonite composite hydrogels in uptake of uranyl ions from aqueous solutions

Uranyl ion (UO₂²⁺) sorption properties of polyelectrolyte composite hydrogels made by the polymerization of acrylamide (AAm) with 2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid (AMPS) and clay such as bentonite (Bent) were investigated as a function of composition to find materials with swelling and uranyl ion sorption properties. Highly swollen AAm/AMPS hydrogels and AAm/AMPS/Bent composite hydrogels were prepared by free radical solution polymerization in aqueous solutions of AAm with AMPS as co‐monomer and two multifunctional crosslinkers such as ethylene glycol dimethacrylate (EGDMA) and 1,4 butanediol dimethacrylate (BDMA). Swelling experiments were performed in water at 25°C, gravimetrically. The influence of AMPS content in hydrogels was examined. Uranyl ion adsorption from aqueous solutions was studied by batch sorption technique at 25°C. The effect of uranyl ion concentration and mass of AMPS on the uranyl ion adsorption were examined. Finally, adsorption capacity (the amount of sorbed uranyl ion per gram of dry hydrogel) (q) was calculated to be 0.67 × 10⁻³–2.11 × 10⁻³ mol uranyl ion per gram for the hydrogels. Removal effiency of uranyl ions (RE%) was changed range 9.05–29.92%. The values of partition ratio (K_d) of uranyl ions was calculated to be 0.10–0.43 for AAm/AMPS hydrogels and AAm/AMPS/Bent composite hydrogels, respectively. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

A new composite sorbent for water and dye uptake: Highly swollen acrylamide/2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid/clay hydrogels crosslinked by 1,4‐butanediol dimethacrylate

A novel type of highly swollen hydrogels based on acrylamide (AAm) with 2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid (AMPS) and clay such as bentonite (Bent) crosslinked by 1,4‐butanediol dimethacrylate (BDMA) was prepared by free radical solution polymerization in aqueous media. Water uptake and dye sorption properties of polyelectrolyte AAm/AMPS hydrogels and AAm/AMPS/Bent composite hydrogels were investigated as a function of composition to find materials with swelling and sorption properties. FTIR analyses were made. Swelling experiments were performed in water and dye solution at 25°C, gravimetrically. Highly swollen AAm/AMPS and AAm/AMPS/Bent hydrogels were used in experiments on sorption of water‐soluble monovalent cationic dye such as Lauths violet “LV, (Thionin).” Swelling of AAm/AMPS hydrogels was increased up to 1,920–9,222% in water and 867–4,644% in LV solutions, while AAm hydrogels swelled 905% in water and swelling of AAm/AMPS/Bent hydrogels was increased up to 2,756–10,422% in water and 1,200–3,332% in LV solutions, while AAm/Bent hydrogels swelled 849% in water. Some swelling kinetic and diffusional parameters were found. Water and LV diffusion into hydrogels was found to be non‐Fickian in character. For sorption of cationic dye, LV into AAm/AMPS and AAm/AMPS/Bent hydrogel was studied by batch sorption technique at 25°C. The amount of the dye sorbed per unit mass removal effiency and partition coefficient of the hydrogels was investigated. The influence of AMPS content in the hydrogels to sorption was examined. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Swelling Characterization of Polyelectrolyte Poly(Hydroxamic Acid) Hydrogels in Aqueous Thiazin Dye Solutions

In this study, swelling behavior of polyelectrolyte poly(hydroxamic acid) (PHA) hydrogels have been investigated in aqueous thiazin dye solutions. PHA hydrogels were prepared by free radical polymerizations of acrylamide with some cross-linkers such as N,N′ methylenebisacrylamide (NBisA) and ethylene glycol dimethacrylate (EGDMA); then they were used in experiments on swelling and diffusion of some water-soluble cationic dyes such as methylene blue (MB), thionin (T), and toluidin blue (TB). Swelling experiments were performed in water at 25°C, gravimetrically. The equilibrium swelling percent (S%) values of PHA hydrogels were calculated as 238–2705%. Some swelling kinetic parameters such as initial swelling rate, swelling rate constant, and maximum (theoretical) swelling percent were found. Diffusional behavior of dye solutions was investigated. Dye diffusion into hydrogels was found to be non-Fickian in character. Diffusion exponent (n) is over 0.50. For sorption of thiazin cationic dyes, MB, T, and TB to PHA hydrogels were studied by batch sorption technique at 25°C. PHA hydrogels in the dye solutions showed the dark coloration. In the experiments of the adsorption, S-type adsorption in the Giles classification system was found.     

Sorption of Methylene Blue onto Ionic Composite Hydrogels Based on Polyacrylamide and Dextran Sulfate: Kinetics,Isotherms, and Thermodynamics

Ionic composite hydrogels based on polyacrylamide (PAAm) and dextran sulfate (DxS) have been prepared by radical polymerization at two temperatures: +20°C and ?18°C, using DxS as physical entrapped polymer, acrylamide (AAm) monomer, N,N^’-methylenebis(acrylamide) (BAAm) as cross-linking agent, ammonium persulfate as radical initiator, and N,N,N’,N’-tetramethylethylenediamine as accelerator of free-radical polymerization. The PAAm/DxS composite hydrogels were tested as sorbents for Methylene Blue (MB) from aqueous solution by the batch procedure. The effect of contact time, initial dye concentration, and temperature on the dye sorption onto composite hydrogels has been investigated. The modeling of the experimental data by applying different kinetic and isotherm models was also performed.