Swelling dynamics of IPN hydrogels including acrylamide‐acrylic acid‐chitosan and evaluation of their potential for controlled release of piperacillin‐tazobactam

For to be used in controlled releasing of piperacillin‐tazobactam, a series of semi and full IPN type hydrogels composed of acrylic acid (AA), acrylamide (AAm) and Chitosan (CS) were prepared via free‐radical polymerization. Ethylene glycol dimethacrylate (EGDMA) was used for crosslinking of PAAm and PAA chains to form semi‐IPN hydrogels. However, the full‐IPN type hydrogels were prepared by using glutaraldehyde (GA) and EGDMA as cocrosslinkers. Characteristics of the hydrogels were investigated by swelling experiments and SEM and FTIR analysis. Generally, full‐IPN type hydrogels swell much more than the semi‐IPN types. By comparing the full‐IPN type hydrogels in between, it is found that the increasing amount of GA causes the decreasing in S% values from 4860 to 4300%. Releasing of piperacillin‐tazobactam from selected three hydrogels were investigated in phosphate buffer solution at pH = 7.4, 37°C. The kinetic release parameters, n and k were calculated and non‐Fickian type diffusion was established for these hydrogels. The behaviors of the piperacillin‐tazobactam loaded hydrogels in Staphylococcus aureus (S. aureus) and Pseudomonas aeruginosa (P. aeruginosa) culture suspensions were also studied and the statistically significant differences for the microorganism growth values were determined. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

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     

Trititanate‐nanosheet incorporated hydrogels: Self‐initiated photopolymerization and application in photodegradation of methylene violet

Exposing the aqueous mixtures of acrylamide (AAm) monomers and exfoliated trititanate nanosheets (TiNs) to ultraviolet light achieved nanocomposite hydrogels TiNs–PAAm in a facile one‐step synthetic route. The incorporated semiconductor TiNs functioned as a photocatalytic crosslinker, initiating the in situ photopolymerization of monomers and hydrogen‐bonding crosslinking with the polymeric networks to form nanocomposite hydrogels. The resultant hydrogels exhibited good absorption behaviors of methylene violet (MV), and the hydrogel prepared from an AAm/TiNs ratio of 2.46 × 10² g/g exhibited a maximum uptake of 8.4 g MV solution for 1 g. The immobilized TiNs retained high photocatalytic activity in the recyclable photodegradation of MV. It indicated the nanocomposite hydrogels may be considered as a good candidate in wastewater treatment. POLYM. COMPOS., 37:2811–2819, 2016. © 2015 Society of Plastics Engineers     

In situ preparation of polyaniline within neutral,anionic, and cationic superporous cryogel networks as conductive,semi‐interpenetrating polymer network cryogel composite systems

Polyaniline [p(An)], one of the most known conducting polymers, was prepared within superporus nonionic polyacrylamide [p(AAm)], anionic poly(2‐acrylamido‐2‐methyl‐1‐propane sulfonic acid sodium salt) [p(AMPS)], and cationic poly(3‐acrylamidopropyltrimethyl ammonium chloride) [p(APTMACl)] cryogels. After they were synthesized, washed, and dried, the neutral p(AAm), anionic p(AMPS), and cationic p(APTMACl) cryogels were soaked in an ammonium persulfate/aniline solution (1:1.25 ratio) in 1 M hydrochloric acid for the in situ oxidative polymerization of p(An) with the cryogel matrices as templates or reactors. The prepared p(AAm)/p(An), p(AMPS)/p(An), and p(APTMACl)/p(An) semi‐interpenetrating polymer network (semi‐IPN) conductive cryogel composites were characterized with scanning electron microscopy (SEM), Fourier transform infrared spectroscopy, and conductivity analysis. The SEM images revealed that the superporus cryogel networks were almost completely filled with p(An) conductive polymers (CPs). Among the cryogel–CP semi‐IPNs, we found that p(AAm)/p(An) semi‐IPN conductive cryogel composites provided the highest conductivity values of 1.4 × 10^?2 ± 4 × 10^?4 S/cm; this was a 6.4 × 10⁶ fold increase in the conductivity from the values of 2.2 × 10^?9 ± 1 × 10^?10 for p(AAm) cryogels. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44137.     

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     

Swelling kinetics,mechanical properties,and release characteristics of chitosan‐based semi‐IPN hydrogels

Two series of pH‐sensitive semi‐interpenetrating network hydrogels (semi‐IPN) based on chitosan (CS) natural polymer and acrylamide (AAm) and/or N‐hydroxymethyl acrylamide (HMA) monomers by varying the monomer and CS ratios were synthesized by free radical chain polymerization. 5‐Fluorouracil (5‐FU), a model anticancer drug, has been added to the feed composition before the polymerization. The characterization of gels indicated that the drug is molecularly dispersed in the polymer matrix. The swelling kinetics of drug‐loaded gels have decreased with increased HMA content at 37°C in both distilled water and buffer solutions with a pH of 2.1 or 7.4. Elastic modulus of the gels increased with the increase in HMA content and higher CS concentration enhanced the elastic modulus positively. Moreover, cumulative release percentages of the gels for 5‐FU were ca. 10% higher in pH 2.1 than those in pH 7.4 media. It was determined that they can be suitable for the use in both gastric and colon environments. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41886.     

Preparation and Swelling Properties of Temperature‐Sensitive Semi‐Interpenetrating Polymer Networks Composed of Poly[(N‐tert‐butylacrylamide)‐co‐acrylamide] and Hydroxypropyl Cellulose

Summary: Temperature‐responsive hydrogels based on linear HPC and crosslinked P(NTBA‐co‐AAm) were prepared by the semi‐IPN technique. The structure of these semi‐IPN hydrogels was investigated by FT‐IR spectroscopy. An increase in normalized band ratios (A₂₉₈₀/A₁₆₆₅) was observed with increasing HPC content in the initial mixture. The swelling kinetics and water transport mechanism of these semi‐IPN hydrogels were examined and their temperature responsive behaviors were also investigated by measuring equilibrium swelling ratios and pulsatile swelling experiments. The results showed that these semi‐IPN hydrogels underwent a volume phase transition between 18 and 22 °C irrespective of the amounts of MBAAm and HPC. However, below the volume phase transition temperature, their equilibrium swelling ratios were affected by the amount of MBAAm and HPC. The pulsatile swelling experiments indicated that the lower the MBAAm and the higher HPC contents in semi‐IPN hydrogels the faster the response rate temperature change.

Equilibrium swelling ratios of the semi‐IPN P(NTBA‐co‐AAm)/HPC hydrogels in water shown as a function of temperature.     

Interpenetrating polymeric network hydrogels for potential gastrointestinal drug release

New interpenetrating polymeric network (IPN) hydrogels based on chitosan (C), poly(N‐vinyl pyrrolidone) (PVP) and poly(acrylic acid) (PAAc), crosslinked with glutaraldehyde (G) and N,N‘‐methylenebisacrylamide (MBA), were prepared and investigated for potential gastrointestinal drug delivery vehicles utilizing a model drug, amoxicillin. IPN hydrogels were synthesized by simultaneous polymerization/crosslinking of acrylic acid monomer in the presence of another polymer (C) and crosslinker (G, MBA). Three different concentrations of glutaraldehyde were used (0.5, 1.0 and 2.0 w/w) to control the overall porosity of the hydrogels, named C‐P‐AAc/0.5, C‐P‐AAc/1.0 and C‐P‐AAc/2.0, respectively. Spectroscopic and thermal analyses such as Fourier transform infrared spectroscopy, thermogravimetric analysis and thermomechanical analysis were performed for IPN characterization. Equilibrium swelling studies were conducted for pH and temperature response behavior. Swelling studies were also carried out in simulated gastric fluid of pH = 1.1 and simulated intestinal fluid of pH = 7.4 to investigate possible site‐specific drug delivery. It was found that the release behavior of the drug from these IPN hydrogels was dependent on the pH of the medium and the proportion of crosslinker in the IPN. It was observed that amoxicillin release at pH = 7.4 was higher than at pH = 1.1. The analysis of the drug release showed that amoxicillin was released from these hydrogels through a non‐Fickian diffusion mechanism. Copyright © 2007 Society of Chemical Industry     

Preparation of alginate/poly(N‐isopropylacrylamide) semi‐interpenetrating and fully interpenetrating polymer network hydrogels with γ‐ray irradiation and their swelling behaviors

Semi‐interpenetrating polymer network (semi‐IPN) and fully interpenetrating polymer network (full‐IPN) hydrogels composed of alginate and poly(N‐isopropylacrylamide) were prepared with γ‐ray irradiation. The semi‐IPN hydrogels were prepared through the irradiation of a mixed solution composed of alginate and N‐isopropylacrylamide (NIPAAm) monomer to simultaneously achieve the polymerization and self‐crosslinking of NIPAAm. The full‐IPN hydrogels were formed through the immersion of the semi‐IPN film in a calcium‐ion solution. The results for the swelling and deswelling behaviors showed that the swelling ratio of semi‐IPN hydrogels was higher than that of full‐IPN hydrogels. A semi‐IPN hydrogel containing more alginate exhibited relatively rapid swelling and deswelling rates, whereas a full‐IPN hydrogel showed an adverse tendency. All the hydrogels with NIPAAm exhibited a change in the swelling ratio around 30–40°C, and full‐IPN hydrogels showed more sensitive and reversible behavior than semi‐IPN hydrogels under a stepwise stimulus. In addition, the swelling ratio of the hydrogels continuously increased with the pH values, and the swelling processes were proven to be repeatable with pH changes. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4439–4446, 2006     

Improved mechanical strength of p(AAm) interpenetrating hydrogel network due to microgranular cellulose embedding

Here, polyacrylamide [p(AAm)]‐based hydrogels were synthesized via redox polymerization technique in the presence of various amounts of microgranular cellulose (MGCell) such as 0, 10, 25, 50, 100, and 150 mg MGCell/g. The synthesized p(AAm)‐MGCell interpenetrating hydrogels were characterized spectroscopically by FTIR, thermally by TGA analysis, and mechanically via dynamic mechanical measurements. Furthermore, the effect of the amount of MGCell in p(AAm) hydrogels on swelling% (S%) degree and mechanical strength was investigated. It was found that the S% was decreased from 727 ± 9 to 667 ± 6, 642 ± 8 and 619 ± 10, 568 ± 6 for p(AAm)‐MGCell interpenetrating network hydrogels containing 10, 50, 100, and 150 mg MGCell, respectively. On the other hand, the Young modulus of p(AAm)‐based hydrogels increased from 2.8 ± 0.2 kPa to 3.1 ± 0.03, 3.4 ± 0.1, 3.6 ± 0.3 and 4.3 ± 0.3 kPa with the incorporation of 10, 50, 100, and 150 mg MGCell into p(AAm) hydrogels. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44854.     

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     

Preparation and characterization of PAM/SA tough hydrogels reinforced by IPN technique based on covalent/ionic crosslinking

In order to fabricate tough hydrogels with superior formability, polyacrylamide/sodium alginate (PAM/SA) interpenetrating polymer network (IPN) hydrogels were produced with ionically crosslinked SA interpenetrated in covalently crosslinked PAM. TGA results show that the heat resistance of PAM/SA IPN hydrogel is improved as compared to that of the individual component. Swelling studies indicate that increasing either chemical crosslinker content or ionic crosslinking via adding more N,N′‐methylenebisacrylamide (MBA) or SA results in lower ESR. It is concluded by tensile test that loosely crosslinked PAM coupled with tightly crosslinked SA improve mechanical strength for hydrogels based on covalent/ionic crosslinking. PAM/SA hydrogels via “one‐pot” method can form different complex shapes with mechanical properties comparable to conventional double network (DN) gels. The fracture strength of PAM_0.05/SA₂₀ reaches level of MPa, approaching 2.0 MPa. The work strives to provide method to tune mechanical and physical properties for hydrogels, which is hopefully to guide the design of hydrogel material with desirable properties. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41342.     

NaOH modified P(acrylamide) hydrogel matrices for in situ metal nanoparticles preparation and their use in H2 generation from hydrolysis of NaBH4

Crosslinked poly(acrylamide) (p(AAm)) as neutral hydrogel is synthesized via photo polymerization technique, and the amide groups within p(AAm) matrices are converted to strongly ionizable carboxylic acids groups via facile modification route by simple treatment of NaOH to obtained NaOH‐p(AAm) hydrogels. Because of the highly ionizable nature of carboxylate groups within mod‐p(AAm), the swelling and metal ion absorbing capacities are increased tremendously, almost 40 and 7.5 folds, respectively. The Co(II) and Ni(II) metal ions are loaded into NaOH‐p(AAm) hydrogels, and are treated with NaBH₄ to form corresponding metal nanoparticles in situ within mod‐p(AAm) matrices, and used in H₂ generation production from hydrolysis of NaBH₄. Various parameters such as functionality of polymeric matrices, the kinds and the amount of metal nanoparticles, and the temperature effecting the H₂ generation are investigated. Comparable low E_a with the similar researches in the literature, E_a = 20.07 ± 0.05 kJ mol^?1 is obtained in NaBH₄ hydrolysis catalyzed by NaOH‐p(AAM)‐Co composite system. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41106.     

The usability of (sodium alginate/acrylamide) semi-interpenetrating polymer networks on removal of some textile dyes

In this study, (sodium alginate/acrylamide) interpenetrating polymer networks ((NaAlg/AAm)IPN) have been prepared at definite composition. The aqueous solution of 3% (w/v) sodium alginate and 50% (w/v) acrylamide was irradiated with ⁶⁰Co-γ rays at a dose rate of 0.07 kGy/h up to 5 kGy. The percent conversion was determined gravimetrically and 100% gelation was achieved at 5 kGy dose. To understand whether the semi-interpenetrating polymer network of sodium alginate is performed, Fourier Transform Infrared (FTIR) spectra of polyacrylamide (PAAm), sodium alginate, and the semi-interpenetrating polymer network were recorded. It is found that the FTIR spectra of PAAm, NaAlg, and the semi-interpenetrating polymer network are different. The thermograms of PAAm, sodium alginate, and the semi-interpenetrating polymer network were recorded for investigating their thermal character. (NaAlg/AAm)IPN hydrogels were immersed to swell in a solution of pH 7, at a temperature of 25°C. The swelling results at pH 7.0 indicated that (NaAlg/AAm)IPN hydrogel, containing 3% NaAlg showed maximum % swelling in water but swelling increased in the order of water > Magenta > Methylene Blue > Safranine-O > Methyl Violet. Diffusion of water and aqueous solution of dyes within (NaAlg/AAm)IPN hydrogels was found to be of Fickian character at the initial stage of swelling with regard to values calculated for diffusion coefficient of (NaAlg/AAm)IPN hydrogels in water and aqueous solution of dyes. Some diffusion parameters were calculated from swelling of (NaAlg/AAm)IPN in water and dyes and their adsorption isotherms were plotted. In the adsorption experiments, the efficiency of (NaAlg/AAm)IPN hydrogels to adsorb Magenta, Safranine-O, Methylene Blue, and Methyl Violet dyes from water was studied. (NaAlg/AAm)IPN hydrogels showed different adsorption for different aqueous solution of dyes at pH 7.0. Adsorption isotherms were constructed for (NaAlg/AAm)IPN-dye systems. S type adsorption in the Giles classification system was found. Thermal and spectroscopic characterization of semi-interpenetrating polymer network of sodium alginate and acrylamide and dye adsorbed semi-interpenetrating polymer network of sodium alginate and acrylamide was recorded. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

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     

Tyrosinase‐mediated in situ forming hydrogels from biodegradable chondroitin sulfate–tyramine conjugates

Tyrosinase‐mediated crosslinking of chondroitin sulfate–tyramine (CS‐TA) conjugates was successfully applied in the preparation of biodegradable in situ forming hydrogels under physiological conditions. Depending on the polymer concentration, the degree of substitution of TA residue and the tyrosinase concentration, the gelation times ranged from 2.3 to 129 min. Studies on the gel contents of CS‐TA hydrogels showed that their degrees of crosslinking could be controlled by varying the tyrosinase concentrations. CS‐TA hydrogels could be completely degraded by the chondroitinase ABC within a time range from 6 days to 11 weeks. CS‐TA hydrogels possessed highly elastic properties and their storage moduli varied from 120 to 1300 Pa, as determined by rheological analysis. Scanning electron microscopy observation confirmed that CS‐TA hydrogels contained a well‐interconnected pore structure. A live–dead assay demonstrated that NIH 3T3 fibroblasts incorporated in CS‐TA hydrogels retained their viability. In addition, in vitro release of methylene blue (a photodynamic therapy drug) from CS‐TA hydrogels could be effectively sustained by the drug encapsulation in the hydrogels. This study indicates that tyrosinase‐mediated in situ forming CS‐TA hydrogels are promising for biomedical applications including drug release and tissue engineering. © 2012 Society of Chemical Industry     

Structural aspects and nature of swelling medium as equilibrium swelling determinants of acrylamide and cellulosic‐based smart hydrogels

Hydroxypropylcellulose (HPC)‐based interpenetrating networks (IPN) with acrylamide (AAm) were synthesized in aqueous medium by simultaneous γ‐ray initiation in the presence of N,N‐methylenebisacrylamide (N,N‐MBAAm). The effect of the synthetic reaction conditions was evaluated for optimum network yield and networks of cellulose and some of its derivatives were obtained with AAm by using these conditions. FTIR, elemental analysis, and scanning electron micrography (SEM) for various structural aspects have characterized networks. Apart from kinetics of IPN formation, this article discusses swelling response of these novel hydrogels in different swelling media. Swelling behavior was studied as a function of synthetic reaction conditions, structure of cellulosics used, and nature of swelling medium (water, 0.5N NaOH, 0.5N HCl, and 5% NaCl). Equilibrium swelling was observed to depend on both structural and environmental factors. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 1161–1169, 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     

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     

Equilibrium swelling studies of highly swollen acrylamide/mesaconic acid hydrogels

Acrylamide/mesaconic acid (AAm/MA) hydrogels were prepared by free radical solution polymerization in aqueous solution of acrylamide (AAm) with mesaconic acid (MA) as comonomer 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 mesaconic acid content in hydrogels was examined. Swelling of AAm/MA hydrogels was increased up to 2301% (for containing 20 mg MA and crosslinked by EGDMA) to 3296% (for containing 80 mg MA and crosslinked by BDMA), while AAm hydrogels swelled up to 1330% (crosslinked by BDMA) to 1400% (crosslinked by EGDMA). The values of equilibrium water content of the hydrogels are 0.9301–0.9706. Diffusion behavior was investigated. Water diffusion into hydrogels was found to be non‐Fickian in character. Diffusion coefficients of AAm/MA hydrogels were calculated by the short time approximation and found to be from 38.01 × 10^?6 cm² s^?1 to 182.73 × 10^?6 cm² s^?1. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 2253–2259, 2005