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     

Synthesis of an alginate–poly(sodium acrylate‐co‐acrylamide) superabsorbent hydrogel with low salt sensitivity and high pH sensitivity

This article describes the synthesis and swelling behavior of a superabsorbing hydrogel based on sodium alginate (NaAlg) and polyacrylonitrile (PAN). The physical mixture of NaAlg and PAN was hydrolyzed with a solution of NaOH to yield an alginate–poly(sodium acrylate‐co‐acrylamide) [Alg–poly(NaAA‐co‐AAm)] superabsorbent hydrogel. A proposed mechanism for hydrogel formation was suggested, and the structure of the product was established with Fourier transform infrared spectroscopy. The effects of reaction variables were systematically optimized to achieve a hydrogel with a swelling capacity as high as possible. Under the optimized conditions concluded, the maximum capacity of swelling in distilled water was 610 g/g. The absorbency of the synthesized hydrogels was also measured in various salt solutions. The swelling ratios decreased with an increase in the ionic strength of the salt solutions. In addition, the swelling capacity was determined in solutions with pHs ranging from 1 to 13. The Alg–poly(NaAA‐co‐AAm) hydrogel exhibited pH responsiveness, so a swelling–deswelling pulsatile behavior was recorded at pHs 2 and 8. This on–off switching behavior made the hydrogel as a good candidate for the controlled delivery of bioactive agents. Finally, the swelling kinetics of the hydrogels with various particle sizes were preliminarily investigated as well. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2927–2937, 2006     

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     

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 and dye sorption studies of AAm/SA hydrogels crosslinked by glutaraldehyde and divinylbenzene

Highly swollen acrylamide (AAm)/sodium acrylate (SA) hydrogels were prepared by free radical solution polymerization in aqueous solution of AAm with SA as comonomer and two multifunctional crosslinkers such as glutaraldehyde (GL) and divinylbenzene (DVB). Water absorption and percentage swelling were determined gravimetrically. The influence of SA content in hydrogels was examined. Percentage swelling ratio of AAm/SA hydrogels was increased up to 2946–12,533%, while AAm hydrogels swelled up to 1326–1618%. The values of equilibrium water content of the hydrogels are between 0.9297–0.9921. Diffusion behavior was investigated. Water diffusion into hydrogels was found to be non‐Fickian in character. Adsorption properties of AAm/SA hydrogels in aqueous thionin solution have been investigated. Finally, the amount of sorbed thionin per gram of dry hydrogel (q_e) was calculated to be 4.81 × 10^?6?11.69 × 10^?6 mol thionin per gram for hydrogels. Removal efficiency (RE%) of the AAm/SA hydrogels was changed range 37.03–68.82%. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Synthesis and properties of radiation‐induced acrylamide–acrylic acid hydrogels

Acrylamide (AAm)/acrylic acid (AAc) hydrogels in the cylindirical form were prepared by γ‐irradiating binary systems of AAm/AAc with 2.6–20.0 kGy γ‐rays. The effect of the dose and relative amounts of AAc and pH on the swelling properties, diffusion behavior of water, diffusion coefficients, and network properties of hydrogel systems was investigated. The swelling capacities of AAm/AAc hydrogels were in the range of 1000–3000%, while poly(acrylamide) (PAAm) hydrogels swelled in the range of 450–700%. Water diffusion into hydrogels was found to be non‐Fickian‐type diffusion. Diffusion coefficients of AAm/AAc hydrogels were found between 0.79 × 10^?5 and 2.78 × 10^?5 cm² min^?1. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 3570–3580, 2002     

Behavior of semi IPN hydrogels composed of PEG and AAm/SMA copolymers in swelling and uptake of Janus Green B from aqueous solutions

Semi-interpenetrating polymer network (semi IPN) hydrogels of poly(ethylene glycol; PEG) were prepared as a water adsorbent for dye (Janus Green B) sorption. For this, PEG and copolymer of acrylamide/sodium methacrylate (AAm/SMA) were prepared by polymerization of aqueous solution of acrylamide (AAm), sodium methacrylate (SMA) using ammonium persulfate (APS)/N,N,N′,N′-tetramethylethylenediamine (TEMED) as redox initiating pair in presence of PEG and poly(ethylene glycol)dimethacrylate (PEGDMA) as crosslinker. FTIR spectroscopy was used to identify the presence of different repeating units in the semi IPNs. Some swelling and diffusion characteristics were calculated for different semi IPNs and hydrogels prepared under various formulations. Water uptake and dye sorption properties of AAm/SMA hydrogels and AAm/SMA/PEG semi IPNs were investigated as a function of chemical composition of the hydrogels. Janus Green B have used in sorption studies. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

pH‐thermoreversible hydrogels. I. Synthesis and swelling behaviors of the (N‐isopropylacrylamide‐co‐acrylamide‐co‐2‐hydroxyethyl methacrylate) copolymeric hydrogels

A series of pH‐thermoreversible hydrogels that exhibited volume phase transition was synthesized by various molar ratios of N‐isopropylacrylamide (NIPAAm), acrylamide (AAm), and 2‐hydroxyethyl methacrylate (HEMA). The influence of environmental conditions such as temperature and pH value on the swelling behavior of these copolymeric gels was investigated. Results showed that the hydrogels exhibited different equilibrium swelling ratios in different pH solutions. Amide groups could be hydrolyzed to form negatively charged carboxylate ion groups in their hydrophilic polymeric network in response to an external pH variation. The pH sensitivities of these gels also depended on the AAm content in the copolymeric gels; thus the greater the AAm content, the higher the pH sensitivity. These hydrogels, based on a temperature‐sensitive hydrogel, demonstrated a significant change of equilibrium swelling in aqueous media between a highly solvated, swollen gel state and a dehydrated network response to small variations of temperature. pH‐thermoreversible hydrogels were used for a study of the release of a model drug, caffeine, with changes in temperature. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 221–231, 1999     

Environmentally sensitive hydrogels: N‐isopropyl acrylamide/Acrylamide/ Mono‐, Di‐, Tricarboxylic acid crosslinked polymers

Environmentally sensitive hydrogels responsive to various stimuli such as temperature, pH, ionic strength of the medium and the solvent were prepared by using N‐isopropyl acrylamide (NIPAM), acrylamide (AAm) and monomers that have various number of carboxylic acid (XA) functionality using N,N′‐methylene bisacrylamide (Bis) as crosslinker. Hydrogels were prepared via free radical polymerization reaction in aqueous solution. P(NIPAAm‐co‐AAm) and p(NIPAAm‐co‐AAm)/XA hydrogels that contain monoprotic crotonic acid (CA) exhibit a lover critical solution temperature (LCST) at 28°C, whereas p(NIPAAm‐co‐AAm)/IA (IA:itaconic acid), and P(NIPAAm‐co‐AAm)/ACA (ACA:acotonic acid) hydrogels exhibit a lover critical solution temperature at 30.7°C and 34.4°C, respectively. Spectroscopic and thermal analyses were performed for the structural and thermal characterizations of the prepared hydrogel. The swelling experiments as equilibrium swelling percentages by gravimetrically were carried out in different solvents, at different solutions temperature, pH, and ionic strengths to determine their effects on swelling characteristic of hydrogels. POLYM. ENG. SCI., 55:843–851, 2015. © 2014 Society of Plastics Engineers     

Carrageenan‐g‐poly(acrylamide)/poly(vinylsulfonic acid,sodium salt) as a novel semi‐IPN hydrogel: Synthesis,characterization, and swelling behavior

A semi‐interpenetrating polymer network (semi‐IPN) hydrogel based on kappa‐carrageenan (κC) and poly (vinylsulfonic acid, sodium salt) (PVSA) was prepared by graft copolymerization of acrylamide (AAm) using methylenebisacrylamide (MBA) as a crosslinking agent and ammonium persulfate (APS) as an initiator. FTIR spectroscopy was used for confirming the structure of the final product. It was found that the chemical composition of the Semi‐IPN hydrogel is equal to the initial homopolymers and monomer feed compositions. The swelling capacity of the hydrogel was shown to be affected by the MBA, APS, and AAm concentration as well as κC/PVSA weight ratio. The swelling behavior of the hydrogel was also investigated in various pHs and salt solutions. Since the highly swelling biopolymer‐based hydrogel exhibits low salt‐sensitivity, it may be referred to as an anti‐salt superabsorbent hydrogel. The swelling kinetics of the superabsorbent hydrogels was studied as well. POLYM. ENG. SCI., 47:1388–1395, 2007. © 2007 Society of Plastics Engineers     

Temperature‐responsive characteristics of poly(N‐isopropylacrylamide) hydrogels with macroporous structure

Macroporous poly(N‐isopropylacrylamide) (PNIPA) hydrogels were synthesized by free‐radical crosslinking polymerization in aqueous solution from N‐isopropylacrylamide monomer and N,N‐methylenebis (acrylamide) crosslinker using poly(ethylene glycol) (PEG) with three different number‐average molecular weights of 300, 600 and 1000 g mol^?1 as the pore‐forming agent. The influence of the molecular weight and amount of PEG pore‐forming agent on the swelling ratio and network parameters such as polymer–solvent interaction parameter (χ) and crosslinking density (ν_E) of the hydrogels is reported and discussed. Scanning electron micrographs reveal that the macroporous network structure of the hydrogels can be adjusted by applying different molecular weights and compositions of PEG during polymerization. At a temperature below the volume phase transition temperature, the macroporous hydrogels absorbed larger amounts of water compared to that of conventional PNIPA hydrogels, and showed higher equilibrated swelling ratios in aqueous medium. Particularly, the unique macroporous structure provides numerous water channels for water diffusion in or out of the matrix and, therefore, an improved response rate to external temperature changes during the swelling and deswelling process. These macroporous PNIPA hydrogels may be useful for potential applications in controlled release of macromolecular active agents. Copyright © 2006 Society of Chemical Industry     

Synthesis of copolymeric hydrogels using gamma radiation and their utilization in the removal of some dyes in wastwater

Copolymer hydrogels were prepared by γ‐radiation copolymerization of maleic acid (MA) and 2‐hydroxyethylacrylate (HEA) or acrylamide (AAm). The effect of AAm/MA and HEA/MA composition and irradiation dose on the gel fraction yield in the prepared hydrogels was determined. It was found that as the content of MA increased, the gel fraction yield decreased. The increase of irradiation dose resulted in increasing the crosslinked network structure and consequently the gel percent. The parameters of equilibrium swelling, maximum swelling, initial swelling rate, diffusion exponent, and diffusion coefficient of the hydrogels were calculated and evaluated, and it was found that water diffusion to the hydrogels generally was a non‐Fickian diffusion type. Characterization of the prepared hydrogels was studied and accordingly the possibility of its practical use in the treatment of waste dyes from aqueous solution was studied. The effect of treatment time, the pH of the feed solution, initial feed concentration, and temperature on the dye uptake was also investigated. The maximum uptake of the investigated dyes was higher for HEA/MA hydrogel than that for AAm/MA hydrogel. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102:3720–3731, 2006     

Swelling characteristics of thermo‐ sensitive poly[(2‐diethylaminoethyl methacrylate)‐co‐(N,N‐dimethylacrylamide)] porous hydrogels

Temperature‐sensitive poly[(2‐diethylaminoethyl methacrylate)‐co‐(N,N‐dimethylacrylamide)] [P(DEAEMA‐co‐DMAAm)] hydrogels with five different DMAAm contents were synthesized with and without the addition of sodium carbonate as porosity generator. The synthesized hydrogels were characterized with dry gel density measurements, scanning electron microscopy observation and the determination of swelling ratio. The influence of the pore‐forming agent and content of DMAAm on swelling ratio and network parameters such as polymer–solvent interaction parameter (χ), average molecular mass between crosslinks (M?_c) and mesh size (ζ) of the cryogels are reported and discussed. The swelling and deswelling rates of the porous hydrogels are much faster than for the same type of hydrogels prepared via conventional methods. At a temperature below the volume phase transition temperature, the macroporous hydrogels also absorbed larger amounts water compared to that of conventional hydrogels and showed obviously higher equilibrated swelling ratios in aqueous medium. In particular, the unique macroporous structure provided numerous water channels for water diffusion in or out of the matrix and, therefore, an improved response rate to the external temperature changes during the deswelling and swelling processes. These properties are attributed to the macroporous and regularly arranged network of the porous hydrogels. Scanning electron micrographs reveal that the macroporous network structure of the hydrogels can be adjusted by applying porosity generation methods during the polymerization reaction. Copyright © 2007 Society of Chemical Industry     

Multiporous microstructure for enhancing the water absorption and swelling rate in poly(sodium acrylic acid) superabsorbent hydrogels based on a novel physical and chemical composite foaming system

In this article, we report a novel physical and chemical composite foaming system, which was used to successfully prepare high‐performance and low‐cost composite superabsorbent [poly(sodium acrylic acid) (PAA–Na)] hydrogels based on acrylic acid by free‐radical polymerization in a water bath under a nitrogen atmosphere without the use of any organic solvents. The prepared hydrogels showed superabsorbent properties, high water‐absorption abilities and swelling rates, a lighter packing density, and a multiporous microstructure. Fourier transform infrared spectroscopy and scanning electron microscopy revealed that the sodium dodecyl sulfate surfactant, sodium bicarbonate chemical foaming agent, and 1,1,2‐trifluorotrichloroethane physical foaming agent were evenly distributed and grafted onto the PAA–Na matrix. Water‐absorption, swelling rate, and packing density testing confirmed that the superabsorbent had a high water‐absorption ability and swelling rate and a lighter packing density. Furthermore, we investigated the effects of different foaming agents, including chemical and physical foaming agents, on the swelling and water‐retention capabilities of the superabsorbent hydrogels (SAHs).The results show that the combination of these foaming agents significantly improved the water‐absorbing capacity. With the help of these foaming agents, we obtained PAA–Na hydrogels without any organic solvents for posttreatment or special porogens; this is an environmentally beneficial way to prepare SAHs for hygiene and biomedical products. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44149.     

Radiation Induced Superabsorbent Hydrogels. Acrylamide/Itaconic Acid Copolymers

Acrylamide/itaconic acid hydrogels in the form of rods are prepared by γ‐irradiation of ternary mixtures of acrylamide/itaconic acid/water with 2.00–5.71 kGy γ‐rays. Spectroscopic and thermal characterization of the copolymers were examined. Dynamic and equilibrium swelling behavior of superabsorbent acrylamide/itaconic acid hydrogels was investigated in water. The equilibrium swelling degree, the swelling rate coefficient, the diffusion constant, the diffusion exponent, the diffusion coefficient, and the intrinsic diffusion coefficient of acrylamide/itaconic acid hydrogels were calculated. The superabsorbent hydrogels have shown mass swelling capabilities in the range 650–700% (for polyacrylamide hydrogels) and 900–2100% (for acrylamide‐itaconic acid hydrogels). Diffusion type of the hydrogels is non‐Fickian diffusion. The equilibrium swelling studies were used to determine important parameters of the crosslinked structure of the hydrogels, including the average molar mass between crosslinks and crosslink density.     

Synthesis and superswelling behavior of carboxymethylcellulose–poly(sodium acrylate‐co‐acrylamide) hydrogel

In this paper, attention is paid to synthesis and swelling behavior of a superabsorbent hydrogel based carboxymethylcellulose (CMC) and polyacrylonitrile (PAN). The physical mixture of CMC and PAN was hydrolyzed in NaOH solution to yield hydrogel, CMC–poly(NaAA‐co‐AAm). During alkaline hydrolysis, the nitrile groups of PAN were completely converted to a mixture of hydrophilic carboxamide and carboxylate groups followed by in situ crosslinking of the grafted PAN chains. A proposed mechanism for hydrogel formation was suggested and the structure of the product was established using FTIR spectroscopy. The reaction variables affecting the swelling capacity of the hydrogel were systematically optimized to achieve a hydrogel with swelling capacity as high as possible. Swelling measurements of the synthesized hydrogels in various chloride salt solutions indicated a swelling‐loss with increase in the ionic strength of the salt solutions. The pH of the various solutions also affected the swelling of the superabsorbent. Furthermore, the present hydrogels showed a pH‐reversible property. Finally, the swelling kinetics of synthesized hydrogels with various absorbent particle sizes was briefly examined. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

pH‐sensitive dimethylaminoethyl methacrylate (DMAEMA)/acrylamide (AAm) hydrogels: Synthesis and adsorption from uranyl acetate solutions

A random copolymer of dimethylaminoethyl methacrylate (DMAEMA) and acrylamide(AAm) [poly(DMAEMA/AAm)], with a pH‐sensitive character, was prepared by a redox polymerization method. Increasing the DMAEMA content of the gel, the pH, and the ionic strength of the solution decreased the swelling ratios of the hydrogels. The adsorption of poly(DMAEMA/AAm) hydrogels from uranyl acetate (UA) solutions was studied at different pHs. The adsorption capacity of hydrogels increased from 200 to 1200 mg of UA per gram of dry hydrogel with increasing pH of the adsorption solution. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2028–2031, 2003     

Swelling behavior and determination of diffusion characteristics of acrylamide–acrylic acid hydrogels

In this study, a random copolymer of acylamide and acrylic acid [poly(AAm‐co‐AA)] was prepared by a redox copolymerization method of their aqueous solutions. The effects of initial AAm/AA mole ratio, PEG 4000 content, and N,N′‐methylenebisacrylamide concentration on swelling behavior were investigated in water. Average molecular weights between crosslinks, percentage swelling, swelling equilibrium values, and diffusion/swelling characteristics (i.e., the structure of network constant, the type of diffusion, the initial swelling rate, swelling rate constant) were evaluated for every hydrogel systems. The hydrogels showed mass swelling capabilities in the range 789–1040% (for AAm/AA hydrogels), 769–930% (for AAm/AA hydrogels in the presence of PEG 4000), and 716–1040% (for AAm/AA hydrogels containing different concentrations of the crosslinker). The swelling capabilities of the hydrogels decreased with the increasing AA, PEG 4000, and crosslinker concentrations. The diffusion of water into AAm/AA hydrogels was found to be a non‐Fickian type. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1289–1293, 2004     

Radiation synthesis and characterization of poly(N‐vinyl‐2‐pyrrolidone/acrylic acid) and poly(N‐vinyl‐2‐pyrrolidone/acrylamide) hydrogels for some metal‐ion separation

Two different hydrogels, prepared from N‐vinyl‐2‐pyrrolidone/acrylic acid (NVP/AAc) and N‐vinyl‐2‐pyrrolidone/acrylamide (NVP/AAm), were studied for the separation and extraction of some heavy‐metal ions from wastewater. The hydrogels were prepared by the γ‐radiation‐induced copolymerization of the aforementioned binary monomer mixtures. Further modification was carried out for the NVP/AAc copolymer through an alkaline treatment to improve the swelling behavior by the conversion of the carboxylic acid groups into its sodium salts. The thermal stability and swelling properties were also investigated as functions of the N‐vinyl‐2‐pyrrolidone content. The characterization and some selected properties of the prepared hydrogels were studied, and the possibility of their practical use in wastewater treatment for heavy metals such as Cu, Ni, Co, and Cr was investigated. The maximum uptake for a given metal was higher for a treated NVP/AAc hydrogel than for an untreated NVP/AAc hydrogel and was higher for an untreated NVP/AAc hydrogel than for an NVP/AAm hydrogel. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 2642–2652, 2004     

Swelling behavior of poly(acrylamide)/clay nanocomposite hydrogels in acrylamide aqueous solution

The swelling behaviors of poly(acrylamide) (PAAm)/clay nanocomposite hydrogels (hereinafter abbreviated as NC gels) in acrylamide (AAm) aqueous solution have been investigated. As‐prepared PAAm/clay hydrogels (S‐M gels) were posttreated by immersing them in AAm aqueous solution. It was found that the swelling ratio of the NC gels increased greatly when the concentration of the solution is below a critical concentration (c*), whereas the gels were disintegrated in the solution when the concentration of the solution is above the c*. Some disc‐like particles were found in the AAm solution accompanying with the unusual swelling behaviors. This unusual swelling behavior is resulted from the change of network structure of the NC gels in AAm aqueous solution, which was further convinced by transmission electron microscopy and element analyses. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009