Synthesis of kappa-carrageenan-g-poly(acrylamide)/sepiolite nanocomposite hydrogels and adsorption of cationic dye

In this study, nanocomposite hydrogels from grafting of acrylamide onto kappa-carrageenan biopolymer were prepared in the presence of sepiolite clay. Methylenebisacrylamide and ammonium persulfate were used as cross-linker and initiator, respectively. The sepiolite nanoclay was introduced into hydrogel matrix without any chemical treatment. The structure of nanocomposites was investigated by FTIR, SEM, TEM, and TGA techniques. The TEM image showed that sepiolite exists as individual needle’s shape. The swelling of hydrogels were studied in distilled water, salt solutions, and various pHs. The obtained nanocomposites were evaluated to remove of cationic crystal violet (CV) dye from water. The kinetic and isotherm of adsorption of dye onto nanocomposites were studied and analyzed according to kinetic and isotherm models. The results showed that the pseudo-second-order adsorption kinetic was predominated for the adsorption of CV onto nanocomposites. The experimental equilibrated adsorption capacity of nanocomposites was analyzed using Freundlich and Langmuir isotherm models. The results corroborated that the experimental data fit the Langmuir isotherm the best. By varying the pH of initial dye solution, while the clay-free hydrogel showed relatively pH-independent adsorption behavior, the nanocomposites depicted pH-dependent adsorption.     

Comparison the properties of PVA/Na+‐MMT nanocomposite hydrogels prepared by physical and physicochemical crosslinking

A novel physicochemical crosslinked nanocomposite hydrogel based on polyvinyl alcohol (PVA) and natural Na‐montmorillonite (Na⁺‐MMT) was synthesized by chemical crosslinking of nanocomposite hydrogel followed by a freezing‐thawing process. The effects of physical crosslinking, as well as physicochemical crosslinking, on the structure, morphology, and properties (thermal, mechanical, swelling, and deswelling) of nanocomposite hydrogels were investigated and compared with each other. The structure and morphology of nanocomposites were studied by Fourier transform infrared, X‐ray diffraction, field emission scanning electron microscopy, and transmission electron microscopy techniques. The thermal and mechanical properties of nanocomposites that were affected by physical and physicochemical crosslinking were evaluated by thermogravimetric analysis, differential scanning calorimeter, dynamic mechanical analysis, hardness test, and Water vapor transmission rate (WVTR) experiments. The results showed that the physicochemical crosslinking of a PVA nanocomposite leads to a reduction in crystallinity and melting temperature, as well as an increase in the Hardness and WVTR compared to a physically crosslinked PVA nanocomposite hydrogel. The swelling and deswelling experiments were performed using a gravimetric method, and it was shown that controlled crosslinking of PVA nanocomposite hydrogel with glutaraldehyde causes the swelling ratio to increase and the cumulative amount of water loss to decrease. The swelling (sorption) and deswelling (desorption) kinetics data for physically and physicochemical crosslinking of nanocomposite hydrogels were fitted with a fickian model. It is concluded that through control crosslinking of PVA nanocomposite can lead to a hydrogel with higher swelling capacity than that is in conventional PVA nanocomposite hydrogel. POLYM. COMPOS., 37:897–906, 2016. © 2014 Society of Plastics Engineers     

Efficient preparation of hybrid nanocomposite coatings based on poly(vinyl alcohol) and silane coupling agent modified TiO2 nanoparticles

In the present investigation, at first, the surface of titanium dioxide (TiO₂) nanoparticles was modified with γ-aminopropyltriethoxy silane as a coupling agent. Then a new kind of poly(vinyl alcohol)/titanium dioxide (PVA/TiO₂) nanocomposites coating with different modified TiO₂ loading were prepared under ultrasonic irradiation process. Finally, these nanocomposites coating were used for fabrication of PVA/TiO₂ films via solution casting method. The resulting nanocomposites were fully characterized by Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), thermogravimetric analysis/derivative thermal gravimetric (TGA/DTG), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and atomic force microscopy (AFM). The TEM and SEM results indicated that the surface modified nanoparticles were dispersed homogeneously in PVA matrix on nanoscale and based on obtained results a possible mechanism was proposed for ultrasonic induced nanocomposite fabrication. TGA confirmed that the heat stability of the nanocomposite was improved. UV–vis spectroscopy was employed to evaluate the absorbance and transmittance behavior of the PVA/TiO₂ nanocomposite films in the wavelength range of 200–800 nm. The results showed that this type of films could be used as a coating to shield against UV light.     

Materials,preparation, and characterization of PVA/MMT nanocomposite hydrogels: A review

This article presents a review of studies on materials, preparation, properties, and characterization of polyvinyl alcohol (PVA) nanocomposite hydrogels. The structure and properties of Montmorillonite, the nanoclay used in the manufacture of PVA nanocomposites and techniques for making PVA nanocomposite hydrogels have been reviewed. The characterization techniques such as Fourier transform infrared spectroscopy (FT‐IR), Differential scanning calorimetry (DSC), Dynamic mechanical analysis (DMA), Scanning electron microscopy, Transmission electron microscopy (TEM), X‐ray diffraction (XRD) are also studied. The XRD patterns and TEM images have proven the intercalated and exfoliated structures of PVA nanocomposite hydrogels that is due to the presence of nanoclay layers. Investigation of FT‐IR spectra shows the bonding formation between OH and silanol groups of PVA and Montmorillonite. Also, the results of DSC and DMA indicated a decrease in crystallinity and the glass transition temperature of PVA by the incorporation of nanoclay, while the loss modulus is increased compared to that of pure PVA. POLYM. COMPOS., 38:1086–1102, 2017. © 2015 Society of Plastics Engineers     

Effect of sodium montmorillonite nanoclay on the water absorbency and cationic dye removal of carrageenan-based nanocomposite superabsorbents

Nanocomposite superabsorbents were synthesized by simultaneously solution copolymerization of acrylamide (AAm) and sodium acrylate (Na-AA) in the presence of carrageenan biopolymer and sodium montmorillonite (Na-MMt) nanoclay. Potassium persulfate (KPS) and methylenebisacrylamide (MBA) were used as initiator and crosslinker, respectively. The structure and morphology of the nanocomposites were investigated using XRD, FTIR, scanning electron microscopy (SEM), and TEM techniques. The influence of nanoclay and carrageenan contents as well as monomer weight ratios on the degree of swelling of nanocomposites was studied. The optimum water absorbency was obtained at 10 wt% of clay, 10 wt% of carrageenan, and 1:1 of monomers weight ratio. The obtained nanocomposites were examined to remove of crystal violet (CV) cationic dye from water. The effect of carrageenan and clay content on the speed of dye adsorption revealed that while the rate of dye adsorption is enhanced by increasing the clay content up to 14 wt% of clay, it was decreased as the carrageenan increased in nanocomposite composition. The results showed that the pseudo-second-order adsorption kinetic was predominated for the adsorption of CV onto nanocomposites. The experimental equilibrated adsorption capacity of nanocomposites was analyzed using Freundlich and Langmuir isotherm models. The results corroborated that the experimental data fit the Freundlich isotherm the best.     

A straightforward preparation and characterization of novel poly(vinyl alcohol)/organoclay/silver tricomponent nanocomposite films

In the present investigation, novel poly(vinyl alcohol)/organoclay/silver (PVA/OMMT/Ag) tricomponent nanocomposite (NC) films with different compositions were prepared by solution intercalation method under ultrasonic irradiation process. The NC films were obtained by mixing a colloidal solution consisting of Ag nanoparticles (NPs) (3, 5, 7 and 9 wt%) with a water solution of PVA and OMMT (10 wt%) via solution casting method. The scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction, Fourier transform infrared spectroscopy, and thermogravimetric analysis (TGA) were utilized to characterize the morphology and properties of the PVA/OMMT/Ag NC films. TGA confirmed that the heat stability of the nanocomposite was improved. The enhancement in the thermal properties of the hybrid materials was due to strong hydrogen bonding between OH groups of PVA, free acid functionalized groups of OMMT, and the Ag NPs. SEM and TEM results also showed that the OMMT and Ag NPs were dispersed homogeneously in the PVA matrix on nanoscale.     

Preparation and characterization of poly(vinyl alcohol) cryogel‐silver nanocomposites and evaluation of blood compatibility,cytotoxicity, and antimicrobial behaviors

In this investigation, cryogels composed of poly(vinyl alcohol) (PVA) were prepared by repeated freeze‐thaw method. The prepared cryogels served as templates for producing highly stable and uniformly distributed silver nanoparticles via in situ reduction of silver nitrate (AgNO₃) using alkaline formaldehyde solution as reducing agent. The structure of the PVA/Ag cryogel nanocomposites was characterized by a Fourier transform infrared and Raman spectroscopy. The morphologies of pure PVA cryogels and PVA/Ag nanocomposites were observed by a scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. The SEM analysis suggested that cryogels show a well defined porous morphology whereas TEM micrographs revealed the presence of nearly spherical and well separated Ag nanoparticles with diameter about 100 nm. XRD results showed all relevant Bragg's reflections for crystal structure of silver nanoparticles. The amount of silver in cryogel nanocomposites and thermal stability were determined by inductively coupled plasma atomic emission spectrometry (ICP‐AES) and thermogravimetric analysis measurements. Mechanical properties of nanocomposites were observed in terms of tensile strength. The antibacterial studies of the synthesized nanosilver containing cryogels showed good antibacterial activity against both gram‐negative and gram‐positive bacteria. The prepared PVA/Ag nanocomposites were also investigated for swelling and deswelling behaviors. The results reveal that both the swelling and deswelling process depends on the chemical composition of the cryogel silver nanocomposites, number of freeze‐Thaw cycles and pH and temperature of the swelling medium. The biocompatibility of the prepared nanocomposites was judged by in vitro methods of percent hemolysis and protein (BSA) adsorption. POLYM. COMPOS., 36:1983–1997, 2015. © 2014 Society of Plastics Engineer     

Physically crosslinked polyvinyl alcohol/chitosan/gum tragacanth hydrogels loaded with vitamin E for wound healing applications

For the healing process, in this study, an innovative polymeric hydrogel network including polyvinyl alcohol (PVA)/chitosan (CS)/gum tragacanth (GT) loaded with vitamin E (VE) was produced by the freeze–thaw approach. In order to investigate the characteristics of the prepared samples, Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM) analyzes were performed. Also, water vapor transmission rate (WVTR), swelling ratio, gel fraction and mechanical properties were measured. Then, to observe their cytocompatibility, MTT assay and cell adhesion studies were assessed. The results of FTIR confirmed the presence of PVA, CS, GT, and VE in hydrogel films. As well as, the SEM images showed the effect of the freezing and thawing method in creating a smooth surface with small and regular pores. It was found with adding the CS and GT to PVA improves swelling ratio, gel fraction, WVTR and elongation of hydrogel films. Further, in examining the adhesion and cytotoxicity of the samples, the non-toxic quiddity of the PVA/CS/GT hydrogel films was corroborated. In the end, the antibacterial properties revealed that the film containing GT and CS had the greatest antibacterial activity. According to the observed results, PVA/CS/GT hydrogel films loaded with VE can be good for wound healing applications.     

Radiation synthesis and characterization of poly(vinyl alcohol)/poly(N-vinyl-2-pyrrolidone) based hydrogels containing silver nanoparticles

A series of PVA/PVP based hydrogels at different compositions were prepared by gamma irradiation. The gel fraction degree of swelling were investigated. Highly stable and uniformly distributed silver nanoparticles have been obtained onto hydrogel networks. The morphology and structure of (PVA/PVP) hydrogel and dispersion of the silver nanoparticles in the polymeric matrix were examined by scanning electron microscopy (SEM) and infrared spectroscopy (FT-IR), respectively. The formation of silver nanoparticles has been confirmed by ultraviolet visible (UV–vis) spectroscopy. A strong characteristic absorption peak was found to be around 420 nm for the silver nanoparticles in the hydrogel nanocomposite. The X-ray diffraction pattern confirmed the formation of silver nanoparticles with average particle size of 12 nm. The diameter distribution of silver nanoparticles was determined by dynamic light scattering DLS. Transmission electron microscope (TEM) showed almost spherical and uniform distribution of silver nanoparticles through the hydrogel network and the mean size of silver nanoparticles ranging is 23 nm. The good swelling properties and antibacterial of PVA/PVP-Ag hydrogel suggest that it can be a good candidate as wound dressing.     

Novel carrageenan-based hydrogel nanocomposites containing laponite RD and their application to remove cationic dye

Novel hydrogel nanocomposites were synthesized by solution polymerization of acrylamide in the presence of carrageenan biopolymer and laponite RD clay. Laponite was used as an inorganic cross-linker. Ammonium persulfate was applied as an initiator. The structure and morphology of the nanocomposites were investigated using XRD, scanning electron microscopy, and transition electron microscopy techniques. The influence of both laponite nanoclay and the carrageenan content on the swelling degree of nanocomposites was studied and it was found that all nanocomposites containing carrageenan component have a high swelling degree compared to a nanocomposite without carrageenan. The obtained nanocomposites were examined to remove a cationic crystal violet (CV) dye from water. The effect of carrageenan and clay contents on the speed of dye adsorption revealed that while the rate of dye adsorption is enhanced by increasing the clay content, it was depressed as the carrageenan content increased in nanocomposite composition. The results showed that the pseudo-second-order adsorption kinetic was predominant in adsorption of CV onto nanocomposites. The experimental equilibrated adsorption capacity of nanocomposites was analyzed using Freundlich and Langmuir isotherm models. The results indicated that the experimental data fit the Langmuir isotherm best. Maximum adsorption capacity was obtained for carrageenan-free nanocomposite with 79.8?mg?g^?1 of adsorbed CV onto nanocomposite.     

Laser transmission welding of poly(lactic acid) and polyamide66/sepiolite nanocomposites

Influence of sepiolite nanoclay on the properties of the resulting join between poly(lactic acid) (PLA) and different Polyamide66 (PA66)/nanoclay nanocomposites was studied in this work. Six different polymer nanocomposites based on PA66 were manufactured through a melt compounding process by adding a fixed 1.64 wt % of a commercial IR absorber additive and the respective weight percentages of sepiolite to the polymer matrix. Several nanocomposite/PLA joints were finally performed by means of the transmission laser welding technology and the resulting weldings were characterized in terms of mechanical properties by performing peeling and shearing tests. Furthermore, both welded and mechanically tested samples were also analyzed by scanning electron microscopy in order to study the morphology of the weld seam. The results of the performed tests show that the addition of sepiolite to the PA66 improves the welding performance only in those cases in which the percentage of sepiolite of the nanocomposites is higher than 5 wt %. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46638.     

Mechanical and UV absorption behavior of zinc oxide nanoparticles: reinforced poly(vinyl alcohol-<Emphasis Type="Italic">g</Emphasis>-acrylonitrile) nanocomposite films

In the present work PVA-g-PAN/ZnO nanocomposite films were prepared by free radical graft copolymerization of acrylonitrile on to PVA and subsequent in situ precipitation of ZnO nanoparticles into the polymer matrix. The films were characterized by FTIR, Raman spectroscopy, differential scanning calorimetry (DSC) and Scanning electron microscopy (SEM). The size of the crystallites and extents of crystallinity were ascertained by X-ray diffraction (XRD) analysis. The SEM with energy dispersive X-ray analysis (EDX) showed that the ZnO nanoparticles were uniformly dispersed within the host grafted copolymer matrix. The transmission electron microscopy (TEM) results clearly indicated that the size of nanoparticles varied in the range 10–30 nm. The UV-absorption properties showed that the films were capable of absorbing more than 95% of UV radiations. Photoluminescence (PL) measurements revealed the presence of defects in the synthesized nanocomposite films. The mechanical properties of the PVA-g-PAN/ZnO nanocomposites such as microhardness and tensile strength were also studied.     

Mesua ferrea L. seed oil based acrylate-modified thermostable and biodegradable highly branched polyester resin/clay nanocomposites

Mesua ferrea L. seed oil based highly branched polyester resin was modified by methyl methacrylate through grafting polymerization technique. The nanocomposites of this acrylate-modified polyester and 1–5 wt% loadings of organically modified montmorrilonite (OMMT) nanoclay were prepared by an ex situ technique using strong mechanical mixing and ultrasonication. Formation of nanocomposites was confirmed by X-ray diffractometeric (XRD), scanning electron microscopic (SEM) and transmission electron microscopic (TEM) analyses. The absence of d_{0 0 1} reflections of OMMT in XRD and TEM study revealed the partial exfoliation of OMMT by the polymer chain. The homogeneous surface morphology was also ascertained from SEM. Mechanical and thermal studies of the nanocomposites showed an appreciable improvement in tensile strength and thermal stability by OMMT loading. The enhancement of tensile strength by 2.5 times and thermal stability by 32 °C for 5 wt% OMMT filled nanocomposite was observed compared to that of pristine system. The rheological behavior of the nanocomposites was also investigated and shear thinning was observed. Biodegradation of the nanocomposite films was assayed using two strains of Pseudomonas aeruginosa, SD2 and SD3 and one strain of Bacillus subtilis, MTCC736. The nanocomposites exhibited enhanced biodegradability as compared to pristine acrylate modified polyester. All the results showed the potentiality of the nanocomposites as advanced thin film materials for suitable applications.     

Superabsorbent composite XXII: Effects of modified sepiolite on water absorbency and swelling behavior of chitosan‐g‐poly(acrylic acid)/sepiolite superabsorbent composite

In this work, a series of chitosan‐g‐poly(acrylic acid)/sepiolite (CTS‐g‐PAA/ST) superabsorbent composites containing raw sepiolite, acid‐activated sepiolite, and cation‐exchanged sepiolite were synthesized by free‐radical graft polymerization in aqueous solution, using N,N′‐methylenebisacrylamide as a crosslinker and ammonium persulfate as an initiator. The effects of raw sepiolite, acid‐activated sepiolite, and cation‐exchanged sepoilite on equilibrium water absorbency, swelling rate, and swelling behavior in different pH value solution of superabsorbent composites were systematically investigated. The results from FTIR spectra showed that chitosan and sepiolite participated in graft polymerization reaction with acrylic acid. The introduction of acid‐activated and cation‐exchanged sepiolite into chitosan‐g‐poly(acrylic acid) polymeric network could improve water absorbency and swelling rate compared with that of the raw sepiolite. All prepared samples have similar swelling behavior in different pH solutions and the equilibrium water absorbencies of samples keep roughly constant in the pH range from 4 to 12. POLYM. COMPOS., 2010. © 2009 Society of Plastics Engineers     

Characterization of latex-based isotactic polypropylene/clay nanocomposites

Polypropylene/clay nanocomposite (PCN) containing 1 wt% organo-modified clay was prepared by latex technology, previously successfully applied for preparation of carbon nanotubes (CNTs)/polymer composites. The level of dispersion of organoclay and the microstructure of the resulting PCNs were characterized by means of X-ray diffraction analysis, transmission electron microscopy (TEM), and scanning electron microscopy (SEM). The obtained results have demonstrated that the latex technique represents a promising method for preparation of PP/clay nanocomposites with good dispersion of exfoliated nanoclay particles. The influence of clay nanoparticles on nonisothermal crystallization of PCN was investigated by DSC. The crystallization onset temperature of the matrix rises for about 5 °C when crystallizing from the quiescent melt. Improved thermal stability of PP/nanoclay was observed as evaluated by TGA. The dynamic mechanical analysis reveals an increase in storage modulus of PP matrix in the nanocomposites for 30% over a temperature range, indicating an increase in the stiffness of the material with the addition of organically modified clay.     

Characterization and in vitro drug release properties of chitosan/acrylamide/gold nanocomposite prepared by gamma irradiation

A nanocomposite of (chitosan/polyacrylamide/gold) (Cs/AAm/Au) and (chitosan/polyacrylamide) (Cs/AAm) hydrogel were performed using gamma radiation and employed as a carrier for Cisplatin cancer drug. The structure and morphology were studied by FTIR and FE-SEM, respectively. XRD and TEM confirmed the formation of the nanoconposite. The average particle size ranged between 13 to 27?nm. EDX estimated that the concentration of Au⁰ nanoparticles in (Cs/AAm/Au) nanocomposite was 0.20%. Both (Cs/AAm) and (Cs/AAm/Au) have higher swelling percent and reached the swelling equilibrium within 6?h. The optimum pH of swelling was at pH 7.2. The maximum Cisplatin drug released was 33% for Cs/AAm hydrogel and 96% for Cs/AAm/Au nanocomposite at pH 7.2 through 320 and 410?min, respectively. The release mechanism was found to be followed the non-Fickian diffusion mechanism for both systems. The cytotoxicity against liver cancer (HepG2) was investigated. Cisplatin drug loaded samples (Cs/AAm) drug loaded hydrogel of concentration 100?μg/ml killed 76.4% of the cells and IC₅₀ reached 29?μg/ml whereas (Cs/AAm/Au) drug loaded nanocomposite killed 84.9 of the cells and IC₅₀ reached 22.7?μg/ml.     

Harmless hydrogels based on PVA/Na+‐MMT nanocomposites for biomedical applications: Fabrication and characterization

A series of nanocomposite hydrogels were prepared by a freeze‐thaw process, using polyvinyl alcohol (PVA) as polymer matrix and 0–10 wt% of hydrophilic natural Na‐montmorillonite (Na⁺‐MMT), free from any modification, as composite aggregates. The effect of nanoclay content and the sonication process on the nanocomposite microstructure and morphology as well as its properties (physical, mechanical, and thermal) were investigated. The microstructure and morphology were investigated by Fourier transform infrared spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, atomic force microscopy, and X‐ray diffraction technique. The thermal stability and mechanical properties of nanocomposite hydrogels were examined using thermogravimetric analysis, differential scanning calorimetry, dynamic mechanical analysis; moreover hardness and water vapor transmission rate measurements. It was concluded that the microstructure, morphology, physical (thermal) and mechanical properties of nanocomposite hydrogels have been modified followed by addition of nanoclay aggregates. The results showed that Na⁺‐MMT may act as a co‐crosslinker. Based on the results obtained, the nanocomposite hydrogel PVA/Na⁺‐MMT synthesized by a freeze‐thaw process, appeared to be a good candidate for biomedical applications. POLYM. COMPOS., 38:1135–1143, 2017. © 2015 Society of Plastics Engineers     

Synthesis and Properties of Sepiolite/poly (acrylic acid-co-acrylamide) Nanocomposites

Summary Novel hydrogel nanocomposites, based on sepiolite, acrylic acid (AA), acrylamide (AM), and N,N’-methylenebisacrylamide (MBA), were synthesized by solution copolymerization. The structure, morphology and liquid absorbency of these composites were investigated through FTIR, SEM and the like. The influences of sepiolite, crosslinker content, initiator dosage, neutralization degree of AA and molar ratio of AA/AM on the distilled water absorbency (Q_w), physiological saline solution absorbency (Q_p) were discussed in detail. Results showed that needleshaped sepiolite dispersed in nanoscale, and the grafting of AA and/or AM on the sepiolite surface occurred. Compared with the sepiolite-free hydrogel, sepiolite contributed to liquid absorbency, and at its weight content of 15.0%, Q_w and Q_p were enhanced as high as 11.6% and 14.5%, respectively.     

Characterization and electrical conductivity of poly(ethylene glycol)/polyacrylonitrile/multiwalled carbon nanotube composites

Poly(Lactic acid) (PLA)‐layered silicate nanocomposite films were prepared by solvent casting method. The films were irradiated with Co⁶⁰ radiation facility at dose of 30 kGy. The effect of γ irradiation on mechanical properties of the neat PLA and nanocomposites was evaluated by data obtained from tensile testing measurements. The tensile strength of the irradiated PLA films increased with addition of 1 wt % triallyl cyanurate indicating crosslink formation. Significant ductile behavior was observed in the PLA nanocomposites containing 4 pph of nanoclay. Incorporation of nanoclay particles in the PLA matrix stimulated crystal growth as it was studied by differential scanning calorimetry. The morphology of the nanocomposites characterized by transmission electron microscopy and X‐ray diffraction revealed an exfoliated morphology in the PLA nanocomposite films containing 4 pph of nanoclay. Only very small changes were observed in the chemical structure of the irradiated samples as it was investigated by Fourier transform infrared spectroscopy. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Synthesis,characterization, and enzymatic degradation of chitosan/PEG hydrogel films

Poly(ethyleneglycol) (PEG)/tartaric acid (TA)‐crosslinked chitosan hydrogel (CPT) films were prepared, and the formation of the PEG/TA‐crosslinked structure was confirmed by Fourier transformed infrared (FTIR), nuclear magnetic resonance (NMR), and scanning electron microscope (SEM) measurements. The thermal properties of the crosslinked films were also determined with thermogravimetric analysis (TGA) and differential scanning calorimeter (DSC) analysis. The swelling properties of the films were investigated at different temperature and pH values. It was found that the swelling ratio increased with the decrease of pH value of the surrounding buffer solutions, amount of PEG, and with the increase of temperature. Swelling behavior of the PEG/TA‐crosslinked chitosan hydrogel films depended on pH and reversible with the temperature. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011