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Sample records for radiation-crosslinked poly vinyl

  1. Radiation-crosslinking of shape memory polymers based on poly(vinyl alcohol) in the presence of carbon nanotubes

    Science.gov (United States)

    Basfar, A. A.; Lotfy, S.

    2015-01-01

    Shape memory polymers based on poly(vinyl alcohol) (SM-PVA) in the presence of 2-carboxyethyl acrylate oligomers (CEA) and multi-wall carbon nanotubes (MWCNTs) crosslinked by ionizing radiation were investigated. Chemical-crosslinking of PVA by glutaraldehyde in the presence of CEA and MWCNTs was also studied. The swelling and gel fraction of the radiation-crosslinked SM-PVA and chemically crosslinked systems were evaluated. Analysis of the swelling and gel fraction revealed a significant reduction in swelling and an increase in the gel fraction of the material that was chemically crosslinked with glutaraldehyde. The radiation-crosslinked SM-PVA demonstrated 100% gelation at an irradiation dose of 50 kGy. In addition, radiation-crosslinked SM-PVA exhibited good temperature responsive shape-memory behavior. A scanning electron microscopy (SEM) analysis was performed. The thermal properties of radiation-crosslinked SM-PVA were investigated by a thermogravimetric analysis (TGA) and dynamic mechanical analysis (DMA). The ability of the material to return or store energy (E‧), to its ability to lose energy (E″), and the ratio of these effects (Tanδ), which is called damping were examined via DMA. The temperature of Tanδ in the radiation-crosslinked SM-PVA decreased significantly by 6 and 13 °C as a result of the addition of MWCNTs. In addition, the temperature of Tanδ for SM-PVA increased as the irradiation dose increased. These radiation-crosslinked SM-PVA materials show promising shape-memory behavior based on the range of temperatures at which Tanδ appears.

  2. The effect of plasticiser on the properties of radiation crosslinked poly(vinyl chloride)

    International Nuclear Information System (INIS)

    Jamaliah Shariff; Roslin Abu Bakar

    1996-01-01

    A study on the effects of plasticizers in the crosslinking of poly(vinyl chloride), PVC, by an electron beam irradiation was carried out. Different types of plasticizers were used and these, with other additives, were blended with PVC in a Brabender mixer. The blended compound was the irradiated with high energy electron beam. Subsequent analysis of its properties showed that the efficiency of crosslinking was better in the presence of the adipate and trimellitate. The tensile and elongation properties were acceptable. The ageing properties of the compounds with adipate and trimellitate-type plasticizers showed encouraging results

  3. Influences of poly (vinyl alcohol molecular weight and carbon nanotubes on radiation crosslinking shape memory polymers

    Directory of Open Access Journals (Sweden)

    Aamer A.M. Alfayyadh

    2017-06-01

    Full Text Available Polyvinyl alcohol (PVA of two molecular weights was used to prepare shape memory polymers based on chemical-crosslinking by glutaraldehyde. The chemical-crosslinking was done in the presence of 2-carboxyethyl acrylate oligomers (CEA and nano-filler [multi-wall carbon nanotubes (MWCNT and functionalized carbon nanotubes (MWCNT-NH2] followed by radiation-induced crosslinking. The analysis of the material revealed an increase in the gel fraction and a significant reduction in swelling of the nanocomposite material that was crosslinked with both glutaraldehyde and ionizing radiation. The radiation crosslinked nanocomposites demonstrated approximately a 90% gelation over a range of 50–300 kGy irradiation doses. The scanning electron microscopy (SEM analysis showed a homogeneous distribution of nanocomposites in the composite matrix. The thermal properties of radiation crosslinked (PVA/CEA and (PVA-CEA-nano-fillers were investigated by a thermogravimetric analysis (TGA. The mechanical properties were examined via dynamic mechanical analysis (DMA which showed significant variation because of the addition of nanocomposites. This radiation crosslinked materials show good shape memory behavior that may be useful in many applications based on the range of temperatures at which Tan δ appears.

  4. Radiation crosslinking of polymer materials and its functional properties

    International Nuclear Information System (INIS)

    Yoshii, Fumio

    2006-01-01

    It was found out that radiation crosslinking of biodegradable polymer such as poly (butylene succinate, PBS) and poly(ε-caprolactone, PCL) could be achieved by radiation in the presence of small amount of trimethallyl isocyanurate (TMAIC) or 1% triallyl isocyanurate (TAIC). Such modification is very effective to improve heat resistance for PBS and PCL. Poly (lactic acid, PLA) undergoes crosslinking effectively with 3% TAIC by radiation. Outstanding feature of these polymers is their biodegradability even after crosslinking. Radiation crosslinking of polysaccharide derivatives such as carboxymethyl-cellulose (CMC) is also achieved in aqueous solution at high concentration (paste-like state). The crosslinking behavior was largely affected by the degree of substitution (DS) and polymer concentration. After removal of water the dry CMC gel is used as water absorbent material. This dry gel is the most effective for removal of large amounts of water from organic wastes, resulting in the acceleration of their fermentation. Measurement of swelling ratio of the dry CMC gel in 0.9% NaCl aqueous solution was carried out to expand application fields for this material. Radiation crosslinked poly (vinyl alcohol) hydrogel was successfully commercialized from July 2004 as wound dressing for accelerated healing. Furthermore, this material was also used as gel protector to prevent shore sore and was further commercialized. (author)

  5. MECHANICAL PROPERTIES OF BLENDS OF PAMAM DENDRIMERS WITH POLY(VINYL CHLORIDE) AND POLY(VINYL ACETATE)

    Science.gov (United States)

    Hybrid blends of poly(amidoamine) PAMAM dendrimers with two linear high polymers, poly(vinyl chloride), PVC, and poly(vinyl acetate), PVAc, are reported. The interaction between the blend components was studied using dynamic mechanical analysis, xenon nuclear magnetic resonacne ...

  6. Poly(vinyl pyrrolidone)-Chitosan implant for endoscopic treatment of vesicoureteral reflux

    International Nuclear Information System (INIS)

    Relleve, Lorna S.; Abad, Lucille V.; Aranilla, Charito T.; Dela Rosa, A.M.; Bolong, David T.; Bisnar, Carlo C.

    2008-01-01

    Radiation-crosslinked poly(vinyl pyrrolidone) (PVP)-Chitosan was prepared as a potential injectable implant for endoscopic treatment of vesicoureteral reflux (VUR). The physical and histological properties of PVP-Chitosan implant in comparison with the commercial dextranomer/hyaluronic acid copolymer (Deflux) have been evaluated in vivo by subcutaneous and abdominal injection in rats over a period of 6 months. The PVP-Chitosan implant was easily injected through 26-gauge needle. Monthly gross examination of the implanted sites showed no significant decrease in volume of implant and no local inflammatory reaction. Histological findings indicated no evidence of migration to the distant organs after 6 months of implantation. Results of this study indicated that PVP-Chitosan implant has properties of a good tissue augmenting substance such as stability, biocompatibility and non-migration but long-term studies are needed to evaluate its therapeutic efficiency. (author)

  7. The radiation crosslinking of ethylene copolymers

    International Nuclear Information System (INIS)

    Burns, N.M.

    1979-01-01

    The enhanced radiation crosslinking tendency of ethylene-vinyl acetate and ethylene-ethyl acrylate copolymers over ethylene homopolymer is proportional to the comonomer content. This is caused by an increase in the amorphous polymer content and by structure-related factors. The copolymers crosslink by a random process that for ethylene-vinyl acetate copolymer involves some crosslinking through the acetoxy group of the comonomer. While knowledge of the process for the crosslinking of ethylene-ethyl acrylate copolymer is less certain, it is currently believed to occur primarily at the branch point on the polymer backbone. Data relating comonomer content and the molecular weight of the copolymers to the radiation crosslinking levels realized were developed to aid in resin selection by the formulator. Triallyl cyanurate cure accelerator was found to be less effective in ethylene-vinyl acetate copolymer than in homopolymer and to have no effect on gel development in ethylene-ethyl acrylate copolymer. (author)

  8. Graft polymerization of vinyl acetate onto starch. Saponification to starch-g-poly(vinyl alcohol)

    International Nuclear Information System (INIS)

    Fanta, G.F.; Burr, R.C.; Doane, W.M.; Russell, C.R.

    1979-01-01

    Graft polymerizations of vinyl acetate onto granular cornstarch were initiated by cobalt-60 irradiation of starch-monomer-water mixtures, and ungrafted poly(vinyl acetate) was separated from the graft copolymer by benzene extraction. Conversions of monomer to polymer were quantitative at a radiation dose of 1.0 Mrad. Over half of the polymer was present as ungrafted poly(vinyl acetate) (grafting efficiency less than 50%), and the graft copolymer contained only 34% grafted synthetic polymer (34% add-on). Lower irradiation doses produced lower conversions of monomer to polymer and gave graft copolymers with lower % add-on. Addition of minor amounts of acrylamide, methyl acrylate, and methacrylic acid as comonomers produced only small increases in % add-on and grafting efficency. Grafting efficiency was increased to 70% when a monomer mixture containing about 10% methyl methacrylate was used. Grafting efficiency could be increased to over 90% if the graft polymerization of vinyl acetate--methyl methacrylate was carried out near 0 0 C; although conversion of monomers to polymer was low and grafted polymer contained 40 to 50% poly(methyl methacrylate). Selected graft copolymers were treated with methanolic sodium hydroxide to convert starch-g-poly(vinyl acetate) to starch-g-poly(vinyl alcohol). The molecular weight of the poly(vinyl alcohol) moiety was about 30,000. The solubility of starch-g-poly(vinyl alcohol) in hot water was less than 50; however, solubility could be increased by substituting either acid-modified or hypochlorite-oxidized for unmodified starch in the graft polymerization reaction. Vinyl acetate was also graft polymerized onto acid-modified starch which had been dispersed and partially solubilized by heating in water. A total irradiation dose of either 1.0 or 0.5 Mrad gave starch-g-poly

  9. Separation of water and oil by poly (acrylic acid)-coated stainless steel mesh prepared by radiation crosslinking

    Energy Technology Data Exchange (ETDEWEB)

    Nho, Young Chang; Shin, Jung Woong; Park, Jong Seok; Lim, Young Mook; Jeun, Joon Pyo; Kang, Phil Hyun [Research Division for Industry and Environment, Korea Atomic Energy Research Institute, Jeongeup (Korea, Republic of)

    2015-05-15

    The stainless steel mesh coated with poly(acrylic acid) hydrogel was fabricated and applied for the separation of water and oil. The stainless steel mesh was immersed in aqueous poly (acrylic acid) solution, and then irradiated by radiation to introduce poly(acrylic acid) hydrogel on the surface of mesh by crosslinking. It was possible to separate oil and water from mixtures of oil/water effectively using the hydrogel-coated mesh. The effect of irradiation dose, coating thickness, size of mesh on the separation efficiency was examined.

  10. Radiation crosslinking of polymer materials

    International Nuclear Information System (INIS)

    Yoshii, Fumio

    2004-01-01

    It was found that some polyfunctional monomers (PFM) like triallyl isocyanurate (TAIC) and trimethallyl isocyanurate (TMAIC) when incorporated at low concentrations, are effective for promotion of crosslinking of biodegradable polymers such as polycaprolactone (PCL), poly(butylene succinate-co-adipate) (PBS) and poly(lactic acid) (PLA). PFM are kneaded with biodegradable polymers at molten condition before irradiation. Radiation crosslinking of PBS and PCL with 1% TAIC gave gel fractions of 80% at 20 kGy. This crosslinking is effective to improve deformation of biodegradable polymers at high temperature. The irradiated materials retained their biodegradability even after crosslinking when subjected to soil burial test. Irradiation at molten state (melting temperature, 340degC) led to crosslinking structures for polytetrafluoroethylene (PTFE). Crosslinked PTFE forms transparent films with high abrasion property and high radiation resistance. High-density polyethylene (HDPE) has a higher gel fraction in irradiation at molten state than irradiation at ordinary temperature. Crosslinked HDPE has been applied as knee joints in order to have high abrasion. Radiation crosslinked polycarbosilane (PCS) fiber gives high heat resistant silicon carbide (SiC) after firing. EB irradiation of PCS is effective to improve strength of product and to inhibit flow during carbonization. SiC, being resistant to high temperature will be applied in turbine and body of rockets. (author)

  11. Preparation of Thermoplastic Poly (vinyl Alcohol), Ethylene Vinyl Acetate and Vinyl Acetate Versatic Ester Blends for Exterior Masonry Coating

    International Nuclear Information System (INIS)

    EL-Nahas, H.H.; Gad, Y.H.; Magida, M.M.

    2013-01-01

    Blend systems including ethylene vinyl acetate (EVA), poly (vinyl alcohol) (PVA) and vinyl acetate versatic copolymer latex (VAcVe) were prepared and used as exterior coatings. Mechanical and thermal properties of the blends were investigated using a testo meter, shore hardness tester, thermogravimetric analysis (TGA) and scanning electron microscopy (SEM). The water resistance of the samples was measured. Effect of ionizing irradiation on gel content, tensile strength and surface hardness were also followed. The blend offers binder base for exterior masonry coating systems having superior water resistant and mechanical properties

  12. Radiation crosslinking of poly(butyl acrylate) during polymerization and grafted copolymerization with Cr(III) crosslinked collagen

    International Nuclear Information System (INIS)

    Pietrucha, K.; Kroh, J.

    1984-01-01

    Enhanced crosslinking of synthetic polymer simultaneous with grafting and homopolymerization processes have been observed in irradiated leather tanned with Cr(III) and embedded with aqueous emulsions of butyl acrylate. Extent of poly(butyl acrylate) crosslinking during copolymerization was found to be approximately one order higher than in the case of radiation polymerization of butyl acrylate in emulsion. New method for isolation of grafted copolymer based on degradation of collagen has been developed. The extent of crosslinking was calculated from the swelling data. (author)

  13. Radiation crosslinking of poly(butyl acrylate) during polymerization and grafted copolymerization with Cr(III) crosslinked collagen

    International Nuclear Information System (INIS)

    Pietrucha, K.; Kroh, J.

    1986-01-01

    Enhanced crosslinking of synthetic polymer simultaneously with grafting and homopolymerization processes has been observed in irradiated leather tanned with Cr(III) and embedded with aqueous emulsions of butyl acrylate. The extent of poly(butyl acrylate) crosslinking during copolymerization was found to be approximately one order higher than in the case of radiation polymerization of butyl acrylate in emulsion. A new method for isolation of grafted copolymer based on degradation of collagen has been developed. The extent of crosslinking was calculated from the swelling data. (author)

  14. Preparation of poly (vinyl alcohol) membranes grafted with n-vinyl pyridine/ acrylic acid binary monomers

    International Nuclear Information System (INIS)

    Ajji, A.; Ali, A.

    2014-03-01

    Poly(vinyl alcohol) films were grafted with two monomers using gamma radiation, acrylic acid and N-vinyl pyridine. The influence of different parameters on the grafting yield was investigated as: the comonomer concentration and composition, and irradiation dose. The suitable conditions of the process had been determined to prepare PVA membranes have both properties of the two monomers, acrylic acid and vinyl pyridine as comonomer concentration and composition, and irradiation dose. Some properties of the membranes had been investigated as maximum swelling and grafting. Also the ability of the grafted films to adsorb some heavy metals and dyes was elaborated and discussed.(author)

  15. Radiation crosslinking of polypropylene

    International Nuclear Information System (INIS)

    Nojiri, A.; Sawasaki, T.

    1984-01-01

    The radiation crosslinking of polypropylene with several kinds of polyfunctional monomers has been examined, and it has been clarified that the enhanced crosslinking may be classified into two types. In particular, the irradiation crosslinking process of polypropylene containing a polyfunctional monomer having an acryloyloxy group giving a specific gel - dose curve has been studied by infrared absorption spectrum and oxygen absorptivity measurement in comparison with the non-enhanced system. (author)

  16. Synthesis and characterisation of polymeric nanofibers poly (vinyl alcohol) and poly (vinyl alcohol)/silica using indigenous electrospinning set up

    Energy Technology Data Exchange (ETDEWEB)

    Sasipriya, K.; Suriyaprabha, R.; Prabu, P.; Rajendran, V., E-mail: veerajendran@gmail.com [Centre for Nanoscience and Technology, K. S. Rangasamy College of Technology, Tamil Nadu (India)

    2013-11-01

    Indigenous design and fabrication horizontal of electrospinning set up was developed to facilitate with double drum conveyor belt system to make ease in harvesting nanofibers rapidly. As a bench mark study, organic-inorganic nanofiber composite was synthesised employing our indigenous electrospinning set up. The aqueous solution of poly (vinyl alcohol) and poly (vinyl alcohol)/silica sol were employed to produce nanofiber mats in order to vary the experimental parameters such as voltage, solvent effect and the effect of catalyst. The synthesised pure electro spun poly (vinyl alcohol) and poly (vinyl alcohol)/silica sol fibers were characterized by Scanning electron microscopy (SEM), Atomic force microscopy (AFM) and Fourier transform infra red spectroscopy (FTIR). According to the results, the fine polymeric nanofibers were achieved in the size range of 100-500 nm for pure poly (vinyl alcohol) fiber and 100-700 nm for polyvinyl alcohol/silica and the constitution of silica in rendering better fiber mats with this double drum set up. (author)

  17. Synthesis and characterisation of polymeric nanofibers poly (vinyl alcohol) and poly (vinyl alcohol)/silica using indigenous electrospinning set up

    International Nuclear Information System (INIS)

    Sasipriya, K.; Suriyaprabha, R.; Prabu, P.; Rajendran, V.

    2013-01-01

    Indigenous design and fabrication horizontal of electrospinning set up was developed to facilitate with double drum conveyor belt system to make ease in harvesting nanofibers rapidly. As a bench mark study, organic-inorganic nanofiber composite was synthesised employing our indigenous electrospinning set up. The aqueous solution of poly (vinyl alcohol) and poly (vinyl alcohol)/silica sol were employed to produce nanofiber mats in order to vary the experimental parameters such as voltage, solvent effect and the effect of catalyst. The synthesised pure electro spun poly (vinyl alcohol) and poly (vinyl alcohol)/silica sol fibers were characterized by Scanning electron microscopy (SEM), Atomic force microscopy (AFM) and Fourier transform infra red spectroscopy (FTIR). According to the results, the fine polymeric nanofibers were achieved in the size range of 100-500 nm for pure poly (vinyl alcohol) fiber and 100-700 nm for polyvinyl alcohol/silica and the constitution of silica in rendering better fiber mats with this double drum set up. (author)

  18. Synthesis and characterisation of polymeric nanofibers poly (vinyl alcohol and poly (vinyl alcohol/silica using indigenous electrospinning set up

    Directory of Open Access Journals (Sweden)

    K. Sasipriya

    2013-01-01

    Full Text Available Indigenous design and fabrication horizontal of electrospinning set up was developed to facilitate with double drum conveyor belt system to make ease in harvesting nanofibers rapidly. As a bench mark study, organic-inorganic nanofiber composite was synthesised employing our indigenous electrospinning set up. The aqueous solution of poly (vinyl alcohol and poly (vinyl alcohol/silica sol were employed to produce nanofiber mats in order to vary the experimental parameters such as voltage, solvent effect and the effect of catalyst. The synthesised pure electro spun poly (vinyl alcohol and poly (vinyl alcohol/silica sol fibers were characterized by Scanning electron microscopy (SEM, Atomic force microscopy (AFM and Fourier transform infra red spectroscopy (FTIR. According to the results, the fine polymeric nanofibers were achieved in the size range of 100-500 nm for pure poly (vinyl alcohol fiber and 100-700 nm for polyvinyl alcohol/silica and the constitution of silica in rendering better fiber mats with this double drum set up.

  19. Synthesis of Poly(vinyl ether) Thermoplastic Elastomers Having Functional Soft Segments

    OpenAIRE

    今枝, 嗣人; 漆崎, 美智遠; 阪口, 壽一; 橋本, 保; Tsuguto, IMAEDA; Michio, URUSHISAKI; Toshikazu, SAKAGUCHI; Tamotsu, HASHIMOTO

    2013-01-01

    The ABA-type triblock copolymers consisting of poly(2-adarnantyl vinyl ether) [poly(2-AdVE) as outer hard segments and poly(6-acetoxyhexyl vinyl ether) [poly(AcHVE)] poly(6-hydroxyhexyl vinyl ether) [poly(H HVE)], or poly(2-(2-methoxyethoxy)ethyl vinyl ether [poly(MOEOVE)] as inner soft segments were synthesized by sequential living cationic polymerization. Despite the presence of polar functional groups such as ester, hydroxy, and oxyethylene units in their soft segments, the two polymer seg...

  20. APPLICATION OF TRITON X-100 COATED POLY VINYL ...

    African Journals Online (AJOL)

    Preferred Customer

    and Zn(II) ions based on the uptake of their complexes with ... The presence of heavy metals in ... Poly vinyl chloride high molecular weight was purchased .... 7.0 and then the charge intensity of the functional groups of solid materials played a ...

  1. Poly(vinyl alcohol) gels as photoacoustic breast phantoms revisited

    NARCIS (Netherlands)

    Xia, Wenfeng; Piras, Daniele; Heijblom, Michelle; Steenbergen, Wiendelt; van Leeuwen, Ton G.; Manohar, Srirang

    2011-01-01

    A popular phantom in photoacoustic imaging is poly(vinyl alcohol) (PVA) hydrogel fabricated by freezing and thawing (F-T) aqueous solutions of PVA. The material possesses acoustic and optical properties similar to those of tissue. Earlier work characterized PVA gels in small test specimens where

  2. Poly(vinyl alcohol) gels as photoacoustic breast phantoms revisited

    NARCIS (Netherlands)

    Xia, W.; Piras, D.; Heijblom, M.; Steenbergen, Wiendelt; van Leeuwen, Ton; Manohar, Srirang

    2011-01-01

    A popular phantom in photoacoustic imaging is poly(vinyl alcohol) (PVA) hydrogel fabricated by freezing and thawing (F–T) aqueous solutions of PVA. The material possesses acoustic and optical properties similar to those of tissue. Earlier work characterized PVA gels in small test specimens where

  3. Radiation-chemical preparation of poly(vinyl alcohol) hydrogels

    International Nuclear Information System (INIS)

    Duflot, Anastasia V.; Kitaeva, Natalia K.; Duflot, Vladimir R.

    2015-01-01

    This work reports the usage of method of radiation-chemical synthesis to prepare cross-linked hydrogels from poly(vinyl alcohol) modified with glycidyl methacrylate. Synthesis kinetics of modified poly(vinyl alcohol) and properties of hydrogels were studied. The gel fraction, swelling, mechanical properties, and water content of the hydrogels were measured. It was found that gel fraction increases with increasing radiation dose, concentration of modified poly(vinyl alcohol), and reaches 60%. It was established by differential scanning calorimetry that a fraction of the “bound” water in hydrogels is 50–70% and independent of gel fraction content. In addition to “bound” and “free” states, water in hydrogels is also present in the intermediate state. - Highlights: • The synthesis and the properties of poly(vinyl alcohol) hydrogels were studied. • PVA was modified by glycidyl methacrylate before gamma cross-linking. • The modification results in decreasing of PVA cross-linking dose by 3 orders lower. • The gel fraction and water content of the hydrogels were measured. • A fraction of the “bound” water in hydrogels is independent of gel fraction content

  4. Preparation of Syndiotactic Poly(vinyl alcohol)/Poly(vinyl pivalate/vinyl acetate) Microspheres with Radiopacity Using Suspension Copolymerization and Saponification

    Science.gov (United States)

    Seok Lyoo, Won; Wook Cha, Jin; Young Kwak, Kun; Jae Lee, Young; Yong Jeon, Han; Sik Chung, Yong; Kyun Noh, Seok

    2010-06-01

    To prepare Poly(vinyl pivalate/vinyl acetate) [P(VPi/VAc)] microspheres with radiopacity, the suspension copolymerization approach in the presence of aqueous radiopaque nanoparticles was used. After, The P(VPi/VAc) microspheres with radiopacity were saponified in heterogeneous system, and then P(VPi/VAc) microspheres without aggregates were converted to s-PVA/P(VPi/VAc) microspheres of skin/core structure through the heterogeneous surface saponification. Radiopacity of microspheres was confirmed with Computed tomography (CT).

  5. Poly(aniline-co-m-aminobenzoic acid) deposited on poly(vinyl ...

    Indian Academy of Sciences (India)

    Abstract. In this work, we have deposited poly(aniline-co-m-aminobenzoic acid) on poly(vinyl alcohol) (PVA) by in situ ... along the polyaniline (PANI) chain results in self dop- ing of PANI and ..... The value of electrical conductivity is found to be ...

  6. Effect of radiation on Poly Vinyl chloride (PVC)

    International Nuclear Information System (INIS)

    Massaud, F.; Haraga, S.; Benfaid, N.; Benayad, S.; Kabar, Y.; Elmesmary, Y; Elwerfeli, M.; Omran, Sh.

    1993-01-01

    Radiation crosslinking of polymeric materials is of increasing commercial importance because of the improved thermal, electrical and mechanical properties. Poly Vinylchloride (PVC) is one of the most important polymers. Many attempts were made to study the primary reactions induced by the direct effect of radiation on PVC. In this study, powder PVC was irradiated with different doses at ambient temperature. Formation of free radicals was investigated by electron spin resonance (ESR) method and molecular weight was determined by viscosity measurements. It has been observed that hydrogen chloride was evolved because of noticeable change in color. One type of radical, Poly enyl structure was trapped at room temperature. The non-symmetric singlet structure of the ESR spectra is due to the presence of oxygen. The radical concentration increased with increase of dose. The molecular weight of irradiated PVC was found to be inversely proportional to the increase of radiation dose, which is believed to be due to the occurrence of degradation. It can be concluded that gamma radiation will be the best method for crosslinking of PVC if multi-functional groups or monomers are present. (author)

  7. Sorption of water vapor in partially hydrolyzed poly(vinyl acetate)

    International Nuclear Information System (INIS)

    Spencer, H.G.; Honeycutt, S.C.

    1973-01-01

    The sorption kinetics of H 2 O and D 2 O in copolymers of partially hydrolyzed poly(vinyl acetate) were studied and compared with the sorption kinetics of vinyl acetate--vinyl alcohol copolymers, and poly(vinyl alcohol). The special measurement problems presented by transient-state sorption studies in water vapor--polymer systems and their effects on the results are discussed

  8. Surface Properties of a Novel Poly(vinyl alcohol Film Prepared by Heterogeneous Saponification of Poly(vinyl acetate Film

    Directory of Open Access Journals (Sweden)

    Seong Baek Yang

    2017-10-01

    Full Text Available Almost general poly(vinyl alcohol (PVA films were prepared by the processing of a PVA solution. For the first time, a novel poly(vinyl alcohol (PVA film was prepared by the saponification of a poly(vinyl acetate (PVAc film in a heterogenous medium. Under the same saponification conditions, the influence of saponification time on the degree of saponification (DS was studied for the preparation of the saponified PVA film, and it was found that the DS varied with time. Optical microscopy was used to confirm the characteristics and surface morphology of the saponified PVA film, revealing unusual black globules in the film structure. The contact angle of the films was measured to study the surface properties, and the results showed that the saponified PVA film had a higher contact angle than the general PVA film. To confirm the transformation of the PVAc film to the PVA film, 1H nuclear magnetic resonance spectroscopy, X-ray diffraction measurements, differential scanning calorimetry, and Fourier-transform infrared spectroscopy were employed.

  9. Williamson alkylation approach to the synthesis of poly(alkyl vinyl ether) copolymers

    International Nuclear Information System (INIS)

    Markova, D.; Christova, D.; Velichkova, R.

    2008-01-01

    A method for synthesis of poly(alkyl vinyl ether-co-vinyl alcohol) copolymers was developed based on the Williamson's alkylation of poly(vinyl acetate) (PVAc) with alkyl iodides. The influence of the alkylating agent and the reaction conditions on the efficiency of the modification reaction was investigated. The copolymers obtained were characterized by means of 1 H NMR and GPC. It was proved that by applying the proposed method copolymers of different composition and properties containing methyl vinyl ether, ethyl vinyl ether as well as n-butyl vinyl ether units could be prepared. Poly(methyl vinyl ether-co-vinyl alcohol)s of high degree of methylation exhibit sharp temperature response at 38-39 deg C in aqueous solution typical of the so-called smart polymers. (authors)

  10. Stereocomplexation of low molecular weight poly(L-lactic acid) and high molecular weight poly(D-lactic acid), radiation crosslinking PLLA/PDLA stereocomplexes and their characterization

    International Nuclear Information System (INIS)

    Quynh, Tran Minh; Mai, Hoang Hoa; Lan, Pham Ngoc

    2013-01-01

    Poly(L-lactic acid)s (PLLAx) were synthesized from L-lactic acid by polycondensation. Different stereocomplexes were also obtained with equimolar mixtures of synthesized PLLAx and a commercial PDLA. The stereocomplexes were crosslinked with triallyl isocyanurate (TAIC) by gamma irradiation. Crosslinking density increased with radiation doses, the heavier the crosslinking network, the lower its swelling degree. The crosslinking structures were introduced in the stereocomplexes inhibiting the mobility for crystallization of PLLA molecules. Thermal and mechanical properties of PLA stereocomplexes were remarkably enhanced by radiation induced crosslinking. PLA stereocomplex does not seem to be degraded by PLLA degrading microorganisms existing in compost at room temperature, but the synthesized PLLA was significantly degraded. - Highlights: ► Complete PLA stereocomplex was obtained from synthesized PLLA and a commercial PDLA. ► Melting temperature of stereocomplex were much improved by gamma irradiation. ► Crosslinking network inhibited the mobility of polymeric chains for crystallization. ► Biodegradability of PLLA was reduced by stereocomplexation and crosslinking.

  11. Graft copolymerization of styrene onto poly(vinyl alcohol) initiated by potassium diperiodatocuprate (III)

    International Nuclear Information System (INIS)

    Bai, L.; Wang, Ch.; Jin, J.; Liu, Y.

    2009-01-01

    The graft copolymerization of styrene onto poly(vinyl alcohol) is studied by using a novel redox system of potassium diperiodatocuprate-poly(vinyl alcohol) (Cu(III)poly(vinyl alcohol) in alkaline medium. Cu(III)-poly(vinyl alcohol) redox pair is an efficient initiator for this graft copolymerization which is proved by high graft efficiency (>97%) and high percentage of graft (>300%). Reaction conditions (monomer-to-poly(vinyl alcohol) weight ratio, initiator concentration, p H, time and temperature) affect the graft parameters which have been investigated systematically. The optimum reaction conditions are found as St/poly(vinyl alcohol) = 5.4; [Cu(III)] = 1*10 -2 M; p H = 12.7; temperature = 50 d eg C ; time = 3.5 h. Further, the equation of the overall polymerization rate can be written as follows: R p = k C 1.9 (St) C 1.7 (Cu(III)). The overall activation energy was calculated to be 42.0 kJ/mol based on the experimental data of the relations between R p and C(St); R p and C(Cu(III)); and R p and temperature. A mechanism is proposed to explain the formation of radicals and the initiation. The structure of the graft copolymers is confirmed by Fourier transfer infrared spectroscopy. Some peaks were compared with poly(vinyl alcohol) at 3080.34-3001.79 cm -1 (=C-H stretching in the phenyl ring), 1600.34-1450.95 cm -1 (C=C stretching in the phenyl ring), 755.17 cm -1 and 698.64 cm -1 (=C-H out-off-plane bending in phenyl ring) which are considered to belong to the characteristic absorption bands of phenyl group of polystyrene. Therefore it proves that the graft copolymer is composed of poly(vinyl alcohol) and polystyrene. thermal gravimetric analysis thermo grams of poly(vinyl alcohol) and poly(vinyl alcohol)-graft-polystyrene are investigated as well. As it is shown the initial decomposition temperature of poly(vinyl alcohol)-g-polystyrene(377.3 d eg C ) is much higher than that of poly(vinyl alcohol) (241.8 d eg C ), which indicates that the thermal stability of the

  12. Plastics piping systems for industrial applications – Acrylonitrile-butadiene-styrene (ABS), unplasticized poly(vinyl chloride) (PVC-U) and chlorinated poly(vinyl chloride) (PVC-C) – Specifications for components and the system – Metric series

    CERN Document Server

    Deutsches Institut für Normung. Berlin

    2003-01-01

    Plastics piping systems for industrial applications – Acrylonitrile-butadiene-styrene (ABS), unplasticized poly(vinyl chloride) (PVC-U) and chlorinated poly(vinyl chloride) (PVC-C) – Specifications for components and the system – Metric series

  13. Plastics piping systems for industrial applications : acrylonitrile-butadiene- styrene (ABS), unplasticized poly(vinyl chloride) (PVC-U) and chlorinated poly(vinyl chloride) (PVC-C) : specifications for components and the system : metric series

    CERN Document Server

    International Organization for Standardization. Geneva

    2003-01-01

    Plastics piping systems for industrial applications : acrylonitrile-butadiene- styrene (ABS), unplasticized poly(vinyl chloride) (PVC-U) and chlorinated poly(vinyl chloride) (PVC-C) : specifications for components and the system : metric series

  14. Effect of Compatibilization on Poly-ε-Caprolactone Grafting onto Poly(ethylene-co-vinyl alcohol

    Directory of Open Access Journals (Sweden)

    Mohamed Taha

    2011-10-01

    Full Text Available The non-miscibility of the reactants during solvent free poly-ε-caprolactone grafting onto poly(ethylene-co-vinyl alcohol (EVOH dramatically affects reaction kinetics. Different solutions were proposed to accelerate the exchange reactions between poly(ethylene-co-vinyl alcohol and poly-ε-caprolactone. Reactions were conducted in a batch reactor or a mini twin-screw extruder. The addition of a poly(ethylene-co-vinyl alcohol-g-poly-ε-caprolactone copolymer increased the compatibility of the reactants and led to a higher reaction rate. This copolymer was either prepared separately and added at the reaction beginning or prepared in situ grafting caprolactone from EVOH. The reactive system evolution was analyzed using molar mass evolution, microstructure characterization, thermal properties and the reactive blend morphology. The compatibilization effect combined with optimized reaction conditions, such as concentration and nature of catalyst and temperature, resulted in an important increase in reaction rates. Among the tested catalysts, 1,5,7-Triazabicyclo [4.4.0]dec-5-ene was a more efficient catalyst for grafting reactions than Tin (II 2-ethylhexanoate.

  15. Swelling and mechanical properties of physically crosslinked poly(vinyl alcohol) hydrogels.

    Science.gov (United States)

    Suzuki, Atsushi; Sasaki, Saori

    2015-12-01

    Physically crosslinked poly(vinyl alcohol) gels are versatile biomaterials due to their excellent biocompatibility. In the past decades, physically crosslinked poly(vinyl alcohol) and poly(vinyl alcohol)-based hydrogels have been extensively studied for biomedical applications. However, these materials have not yet been implemented due to their mechanical strength. Physically crosslinked poly(vinyl alcohol) gels consist of a swollen amorphous network of poly(vinyl alcohol) physically crosslinked by microcrystallites. Although the mechanical properties can be improved to some extent by controlling the distribution of microcrystallites on the nano- and micro-scales, enhancing the mechanical properties while maintaining high water content remains very difficult. It may be technologically impossible to significantly improve the mechanical properties while keeping the gel's high water absorbance ability using conventional fabrication methods. Physical and chemical understandings of the swelling and mechanical properties of physically crosslinked poly(vinyl alcohol) gels are considered here; some promising strategies for their practical applications are presented. This review focuses more on the recent studies on swelling and mechanical properties of poly(vinyl alcohol) hydrogels, prepared using only poly(vinyl alcohol) and pure water with no other chemicals, as potential biomedical materials. © IMechE 2015.

  16. Effect of Saponification Condition on the Morphology and Diameter of the Electrospun Poly(vinyl acetate) Nanofibers for the Fabrication of Poly(vinyl alcohol) Nanofiber Mats

    OpenAIRE

    Seong Baek Yang; Jong Won Kim; Jeong Hyun Yeum

    2016-01-01

    Novel poly(vinyl alcohol) (PVA) nanofiber mats were prepared for the first time through heterogeneous saponification of electrospun poly(vinyl acetate) (PVAc) nanofibers. The effect of varying the saponification conditions, including temperature, time, and concentration of the alkaline solution, on the morphology of the saponified PVA fibers were evaluated by field-emission scanning electron microscopy. At 25 °C, the saponified PVA fibers exhibited a broad diameter distribution. The average f...

  17. Rubber-like poly(vinyl alcohol) gel

    Energy Technology Data Exchange (ETDEWEB)

    Nambu, Masao (Nippon Oil Co. Ltd., Yokohama (Japan). Central Technical Research Lab.)

    1990-09-01

    Anomalous poly (vinyl alcohol) gel has been found in our laboratory since 1980. The gel is prepared by repeated freezing (or freeze-dehydration) of aqueous poly (vinyl alcohol). Experiments establish the fact that anomalous gel is never produced in the course of freezing, but during sustained thawing the gelation does occur. Moreover, it was found that the softening point of the gel increases at 37degC. It is assumed that crystal nuclei are generated on freezing, then on thawing, some of them grow to very fine crystals which act as polymer network-knots (cross-linking). Additional freezing provide other seeds, which grow similarly, and these are accumulated until rubber-like gel is produced. The gel was always water-resistant at 37degC, and the potassium permanganate consumption of the extracted water layer remained far below the official restricted value for medical materials. The gel can be sterilized with gamma-rays or chlorhexidine. Moreover, it satisfies the official standards of acute toxicity, pyrogen, intracutaneous reaction, hemolyzation, and intracorporeal implantation, respectively. Applications to adhesion-preventing membrane (for joint or pericardium), tamponade (for jaw defects), electrode (for electroretinogram or artificial inner ear), artificial denture base and phantoms for magnetic resonance imaging were examined. (author) 54 refs.

  18. Separator Membrane from Crosslinked Poly(Vinyl Alcohol and Poly(Methyl Vinyl Ether-alt-Maleic Anhydride

    Directory of Open Access Journals (Sweden)

    Charu Vashisth Rohatgi

    2015-03-01

    Full Text Available In this work, we report separator membranes from crosslinking of two polymers, such as poly vinyl alcohol (PVA with an ionic polymer poly(methyl vinyl ether-alt-maleic anhydride (PMVE-MA. Such interpolymer-networked systems were extensively used for biomedical and desalination applications but they were not examined for their potential use as membranes or separators for batteries. Therefore, the chemical interactions between these two polymers and the influence of such crosslinking on physicochemical properties of the membrane are systematically investigated through rheology and by critical gel point study. The hydrogen bonding and the chemical interaction between PMVE-MA and PVA resulted in highly cross-linked membranes. Effect of the molecular weight of PVA on the membrane properties was also examined. The developed membranes were extensively characterized by studying their physicochemical properties (water uptake, swelling ratio, and conductivity, thermal and electrochemical properties using differential scanning calorimetry (DSC, dynamic mechanical analysis (DMA, thermo-gravimetric analysis (TGA and electrochemical impedance spectroscopy (EIS. The DSC study shows the presence of a single Tg in the membranes indicating compatibility of the two polymers in flexible and transparent films. The membranes show good stability and ion conductivity suitable for separator applications.

  19. Separator Membrane from Crosslinked Poly(Vinyl Alcohol) and Poly(Methyl Vinyl Ether-alt-Maleic Anhydride)

    Science.gov (United States)

    Rohatgi, Charu Vashisth; Dutta, Naba K.; Choudhury, Namita Roy

    2015-01-01

    In this work, we report separator membranes from crosslinking of two polymers, such as poly vinyl alcohol (PVA) with an ionic polymer poly(methyl vinyl ether-alt-maleic anhydride) (PMVE-MA). Such interpolymer-networked systems were extensively used for biomedical and desalination applications but they were not examined for their potential use as membranes or separators for batteries. Therefore, the chemical interactions between these two polymers and the influence of such crosslinking on physicochemical properties of the membrane are systematically investigated through rheology and by critical gel point study. The hydrogen bonding and the chemical interaction between PMVE-MA and PVA resulted in highly cross-linked membranes. Effect of the molecular weight of PVA on the membrane properties was also examined. The developed membranes were extensively characterized by studying their physicochemical properties (water uptake, swelling ratio, and conductivity), thermal and electrochemical properties using differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), thermo-gravimetric analysis (TGA) and electrochemical impedance spectroscopy (EIS). The DSC study shows the presence of a single Tg in the membranes indicating compatibility of the two polymers in flexible and transparent films. The membranes show good stability and ion conductivity suitable for separator applications. PMID:28347019

  20. Alanine/epr pellet dosimeter using poly(vinyl butyral-co-vinyl alcohol-co-vinyl acetate) copolymer as a binder for radiation dosimetry

    International Nuclear Information System (INIS)

    Beshir, W.B.; Ezz El-Din, H.M.; Abdel-fatth, A.A.; Ebraheem, S.

    2005-01-01

    A new alanine pellet dosimeter was developed for gamma and electron beam radiation dosimetry. Alanine powder was mixed with a new binding material, poly(vinyl butyral-co-vinyl alcohol-co-vinyl acetate) copolymer. Pellets were prepared by pressing fine powder alanine with 60% copolymer binder by using hydraulic press and a specially designed pressing die. The radiation-formed stable free radicals were analysed by using electron paramagnetic resonance (EPR) spectroscopy. The useful dose range of these pellets was found to ranges from 1 to 80 kGy. The stability of the radiation- induced response was also studied

  1. Effect of gamma radiation on the poly(vinyl alcohol)

    International Nuclear Information System (INIS)

    Terence, M.C.; Guedes, S.M.L.

    2000-01-01

    The poly(vinyl alcohol) (PVAL) is a polymer used as bio material. The PVAL was used as ocular insert and may be used as a drug delivery system (DDS) for pair PVAL/gancyclovir, where the last one is used for treatment of people with retinitis caused by cytomegalovirus. These inserts are crosslinked systems. The crosslink was induced by gamma radiation applied in polymer. The samples of PVAL was irradiated by gamma rays with doses in the range 0 to 100 kGy. On irradiated PVAL samples was observed a low yellowness, attributed to the formation of polymeric radicals that are stable in the structure of the polymer, from radiolysis of PVAL. (author)

  2. Viscometric investigation of compatibilization of the poly(vinyl chloride)/poly(ethylene-co-vinyl acetate) blends by terpolymer of maleic anhydride styrene vinyl acetate

    Science.gov (United States)

    İmren, Dilek; Boztuğ, Ali; Yılmaz, Ersen; Zengin, H. Bayram

    2008-11-01

    In this study, a blend of poly(vinyl chloride) (PVC)/ethylene-co-vinyl acetate (EVA) was compatibilized by terpolymer of maleic anhydride-styrene-vinyl acetate (MAStVA) used as a compatibilizer. It was prepared the blends of 50/50 PVC/EVA containing 2-10% of the terpolymer. The compatibility experiences of these blends were investigated by using viscometric method in the range of concentrations (0.5-2.0 g dL -1) where tetrahydrofuran (THF) is the solvent. The interaction parameter (Δ b) was used to study the miscibility and compatibility of polymer blend in solution, obtained from the modified Krigbaum and Wall theory. Turbidity and FTIR measurements were also used to investigate the miscibility of this pair of polymers. The values of the relative viscosities of the each polymer solution and their blends were measured by a Cannon-Fenske type viscometer. In consequence of the study, it was observed that a considerable improvement was achieved in the miscibility of PVC/EVA blends by adding among 5 and 10 wt% of compatibilizer.

  3. Properties of poly(vinyl alcohol)–borax gel doped with neodymium ...

    Indian Academy of Sciences (India)

    visible region then leads to luminescent emission in the near infra-red region. The spectral qualities of the ... molecular hydrogen bonding between the hydroxyl groups on poly(vinyl ..... mately results in near IR emissions. The maximum of the.

  4. Laser induced augmentation of silver nanospheres to nanowires in ethanol fostered by Poly Vinyl Pyrrolidone

    Energy Technology Data Exchange (ETDEWEB)

    Sebastian, Suneetha, E-mail: sunikutty@gmail.com; Linslal, C.L.; Vallabhan, C.P.G.; Nampoori, V.P.N.; Radhakrishnan, P.; Kailasnath, M.

    2014-11-30

    Highlights: • Silver nanospheres are synthesised in ethanol containing Poly Vinyl Pyrrolidone which acts as a polymeric capping agent to nanoparticles thus improving its stability. • Laser irradiation onto the colloidal solution of silver nanoparticles produced well defined nanowires through ripening mechanism promoted by Poly Vinyl Pyrrolidone. • Nanowires so formed are having an average length of 8.7 μm and width of 160 nm. - Abstract: Stable uniform silver nanospheres having an average diameter of 45 nm are synthesised in ethanol containing Poly Vinyl Pyrrolidone using Laser Ablation in Liquid technique. Further irradiation of the nanocolloidal solution by focussed laser beam produced stable well defined silver nanowires through ripening mechanism fostered by the presence of Poly Vinyl Pyrrolidone. Confirmation of the mechanism is obtained from Transmission Electron Microscopic images of the nanocolloidal solution irradiated for different time durations.

  5. The Effects of Reaction Variables on Solution Polymerization of Vinyl Acetate and Molecular Weight of Poly(vinyl alcohol Using Taguchi Experimental Design

    Directory of Open Access Journals (Sweden)

    M.H. Navarchian

    2009-12-01

    Full Text Available Poly(vinyl acetate is synthesized via solution polymerization, and then it is converted to poly(vinyl alcohol by alkaline alcoholysis. The aim of the work study was to investigate statistically the  influence of reaction variables in vinyl acetate polymerization, the conversion of this monomer to polymer, degree of branching of acetyl group in poly(vinyl acetate, as well as the molecular weight of poly(vinyl alcohol, using Taguchi experimental design approach. The reaction variables were polymerization time, molar ratio of initiator to monomer, and volume ratio of monomer to solvent. The statistical analysis of variance of the results revealed that all factors have significantly influenced the conversion and degree of branching. Volume ratio of monomer to solvent is the only factor affecting the molecular weight of poly(vinyl alcohol, and has the greatest influence on all responses. By increasing this ratio, the conversion, degree of branching of acetyl group in poly(vinyl acetate, and molecular weight of poly(vinyl alcohol were increased.

  6. Preparation of poly(vinyl alcohol) membranes grafted with N-vinyl imidazole/acrylic acid binary monomers

    International Nuclear Information System (INIS)

    Ajji, Zaki; Ali, Ali

    2006-01-01

    Poly(vinyl alcohol) films were grafted with two monomers using gamma radiation, acrylic acid and N-vinyl imidazole. The influence of different parameters on the grafting yield was investigated as: type of solvent and solvent composition, comonomer concentration and composition, addition of mineral acids, and irradiation dose. Water uptake in respect to the grafting yield was also evaluated. The ability of the grafted films to adsorb copper ions was elaborated and discussed for different grafting yields and ph values of the solution. (authors)

  7. Pervaporation of alcohol-toluene mixtures through polymer blend membranes of poly(acrylic acid) and poly(vinyl alcohol)

    NARCIS (Netherlands)

    Park, H.C.; Park, H.; Meertens, R.M.; Meertens, R.M.; Mulder, M.H.V.; Smolders, C.A.; Smolders, C.A.

    1994-01-01

    Homogeneous membranes were prepared by blending poly(acrylic acid) with poly(vinyl alcohol). These blend membranes were evaluated for the selective separation of alcohols from toluene by pervaporation. The flux and selectivity of the membranes were determined both as a function of the blend

  8. Raman spectroscopy of poly (3-hydroxybutyrate) modified with poly (vinyl acetate) by radiation- induced copolymerization

    International Nuclear Information System (INIS)

    Gonzalez, Maykel; Galego Fernandez, Norma; Ortiz del Toro, Pedro; Rapado, Manuel; Paredes

    2007-01-01

    Poly (3-hydroxybutyrate) (PHB) is an important material used in the field of medicine. However in common conditions, PHB has some deficiencies. It is very brittle and slightly hydrophobic polymer. This somewhat limit its applications. Radiation chemistry can be used to improve its chemical properties. In the present study, the substrate, modified by radiation-induced graft copolymerization with vinyl acetate (VAc), was characterized using FTIR and Raman spectroscopy. FTIR spectroscopy did not reveal any significant bands but Raman spectroscopy revealed the formation of a new band that characterize the material

  9. Surface studies of microcrystalline chitosan/poly(vinyl alcohol) mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Lewandowska, Katarzyna, E-mail: reol@chem.uni.torun.pl [Nicolaus Copernicus University, Faculty of Chemistry, Chair of Chemistry and Photochemistry of Polymers, 7 Gagarin Street, 87-100 Torun (Poland)

    2012-12-15

    Highlights: Black-Right-Pointing-Pointer The surface properties were investigated by AFM, SEM and FTIR. Black-Right-Pointing-Pointer The AFM images showed the lamellar structure of PVA in the blend. Black-Right-Pointing-Pointer SEM microscopy confirmed the existence of microphase separation of components. Black-Right-Pointing-Pointer FTIR analysis showed the existence of a weak interaction. - Abstract: In the present study, the surface properties of microcrystalline chitosan (MCCh), poly(vinyl alcohol) (PVA) and MCCh/PVA blends (made from acetic acid solutions with the MCCh concentration ranging from 20% to 80%) have been studied by the tapping-mode atomic force microscopy (AFM), scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy. The changes of topography images are considered by determining the root mean square (RMS, R{sub q}) deviation in the image data. For PVA samples, the transition between adjacent lamellae occurs through holes, islands, and bicontinuous structures. The AFM images showed also the lamellar structure of PVA in the blend. The crystalline topography of MCCh/PVA film surface suggests the presence of PVA on the top surface. The FTIR spectra of film blends, in the amide I and II region of MCCh and the hydroxyl stretching bands of PVA have been analyzed. FTIR analysis showed the existence of a weak interaction of the hydroxyl or amino groups of microcrystalline chitosan with hydroxyl groups of PVA.

  10. Poly(vinyl alcohol) gels as photoacoustic breast phantoms revisited.

    Science.gov (United States)

    Xia, Wenfeng; Piras, Daniele; Heijblom, Michelle; Steenbergen, Wiendelt; van Leeuwen, Ton G; Manohar, Srirang

    2011-07-01

    A popular phantom in photoacoustic imaging is poly(vinyl alcohol) (PVA) hydrogel fabricated by freezing and thawing (F-T) aqueous solutions of PVA. The material possesses acoustic and optical properties similar to those of tissue. Earlier work characterized PVA gels in small test specimens where temperature distributions during F-T are relatively homogeneous. In this work, in breast-sized samples we observed substantial temperature differences between the shallow regions and the interior during the F-T procedure. We investigated whether spatial variations were also present in the acoustic and optical properties. The speed of sound, acoustic attenuation, and optical reduced scattering coefficients were measured on specimens sampled at various locations in a large phantom. In general, the properties matched values quoted for breast tissue. But while acoustic properties were relatively homogeneous, the reduced scattering was substantially different at the surface compared with the interior. We correlated these variations with gel microstructure inspected using scanning electron microscopy. Interestingly, the phantom's reduced scattering spatial distribution matches the optical properties of the standard two-layer breast model used in x ray dosimetry. We conclude that large PVA samples prepared using the standard recipe make excellent breast tissue phantoms.

  11. Synthesis of PbS/poly (vinyl-pyrrolidone) nanocomposite

    International Nuclear Information System (INIS)

    Patel, Jayesh D.; Chaudhuri, Tapas K.

    2009-01-01

    A simple solution growth method for synthesis of nanocomposite of PbS nanoparticles in poly(vinyl-pyrrolidone) (PVP) polymer is described. The nanocomposite is prepared from methanolic solution of lead acetate (PbAc), thiourea (TU) and PVP at room temperature (∼27 deg. C). Optical absorption spectrum of PbS/PVP nanocomposite solution shows strong absorption from 300 to 650 nm with significant bands at 400 and 590 nm which is characteristic of nanoscale PbS. Spin-coated nanocomposite films on glass have an absorption edge at ∼650 nm with band gap of 2.55 eV. Fourier transform infrared (FTIR) spectroscopy of PbS/PVP nanocomposite and PVP shows strong chemical bond between PbS nanoparticles and host PVP polymer. The transmission electron microscope (TEM) images reveal that 5-10 nm PbS particles are evenly embedded in PVP polymer. The formation of PbS is confirmed by selective area electron diffraction (SAED) of a typical nanoparticle.

  12. Surface studies of microcrystalline chitosan/poly(vinyl alcohol) mixtures

    International Nuclear Information System (INIS)

    Lewandowska, Katarzyna

    2012-01-01

    Highlights: ► The surface properties were investigated by AFM, SEM and FTIR. ► The AFM images showed the lamellar structure of PVA in the blend. ► SEM microscopy confirmed the existence of microphase separation of components. ► FTIR analysis showed the existence of a weak interaction. - Abstract: In the present study, the surface properties of microcrystalline chitosan (MCCh), poly(vinyl alcohol) (PVA) and MCCh/PVA blends (made from acetic acid solutions with the MCCh concentration ranging from 20% to 80%) have been studied by the tapping-mode atomic force microscopy (AFM), scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy. The changes of topography images are considered by determining the root mean square (RMS, R q ) deviation in the image data. For PVA samples, the transition between adjacent lamellae occurs through holes, islands, and bicontinuous structures. The AFM images showed also the lamellar structure of PVA in the blend. The crystalline topography of MCCh/PVA film surface suggests the presence of PVA on the top surface. The FTIR spectra of film blends, in the amide I and II region of MCCh and the hydroxyl stretching bands of PVA have been analyzed. FTIR analysis showed the existence of a weak interaction of the hydroxyl or amino groups of microcrystalline chitosan with hydroxyl groups of PVA.

  13. Time domain NMR evaluation of poly(vinyl alcohol) xerogels

    Energy Technology Data Exchange (ETDEWEB)

    Rodrigues, Elton Jorge da Rocha; Cavalcante, Maxwell de Paula; Tavares, Maria Ines Bruno, E-mail: mibt@ima.ufrj.br [Universidade Federal do Rio de Janeiro (IMA/UFRJ), Rio de Janeiro, RJ (Brazil). Centro de Tecnologia. Instituto de Macromoleculas Professora Eloisa Mano

    2016-05-15

    Poly(vinyl alcohol) (PVA)-based chemically cross-linked xerogels, both neat and loaded with nanoparticulate hydrophilic silica (SiO{sub 2}), were obtained and characterized mainly through time domain NMR experiments (TD-NMR). Fourier-transform infrared (FT-IR) and wide angle X-ray diffraction (WAXD) analyses were employed as secondary methods. TD-NMR, through the interpretation of the spin-lattice relaxation constant values and related information, showed both cross-linking and nanoparticle influences on PVA matrix. SiO{sub 2} does not interact chemically with the PVA chains, but has effect on its molecular mobility, as investigated via TD-NMR. Apparent energy of activation, spin-lattice time constant and size of spin domains in the sample have almost linear dependence with the degree of cross-linking of the PVA and are affected by the addition of SiO{sub 2}. These three parameters were derived from a single set of TD-NMR experiments, which demonstrates the versatility of the technique for characterization of inorganic-organic hybrid xerogels, an important class of materials. (author)

  14. Self-assembled hemocompatible coating on poly (vinyl chloride) surface

    Energy Technology Data Exchange (ETDEWEB)

    Zha Zhengbao; Ma Yan; Yue Xiuli; Liu Meng [Nanobiotechnology Division, State Key Laboratory of Urban Water Resources and Environment, School of Sciences, Harbin Institute of Technology, Harbin 150001 (China); Dai Zhifei, E-mail: zhifei.dai@hit.edu.cn [Nanobiotechnology Division, State Key Laboratory of Urban Water Resources and Environment, School of Sciences, Harbin Institute of Technology, Harbin 150001 (China)

    2009-11-15

    A stable hemocompatible coating was fabricated by consecutive alternating adsorption of iron (III) and two kinds of polysaccharides, heparin (Hep) and dextran sulfate (DS), onto poly (vinyl chloride) (PVC) surfaces via electrostatic interaction. The fluctuation of contact angles with the alternative deposition of iron (III) and polysaccharides verified the progressive buildup of the mulitilayer coating onto the PVC surface. Atomic force microscopy (AFM) analysis revealed that the PVC surfaces were completely masked by iron-polysaccharides multilayer coatings. The activated partial thromboplastin time (APTT) assay showed that both Hep/Fe{sup 3+}/Hep and DS/Fe{sup 3+}/Hep coated PVC were less thrombogenic than the uncoated one. Chromogenic assay for heparin activity proved definitively that the inhibition of locally produced thrombin was ascribed to the thromboresistance of the surface-bound heparin. Compared with the unmodified PVC surfaces, iron-polysaccharide multilayer coating presented a drastically reduced adhesion in vitro of platelets, polymorphonuclear neutrophil leukocytes (PMN) and peripheral blood mononuclear cells (PBMC). Interestingly, the DS/Fe{sup 3+}/Hep coating was found to exhibit higher hydrophilicity and stability, hence lower non-specific protein adsorption in comparison with Hep/Fe{sup 3+}/Hep coating due to the incorporation of dextran sulfate into the multilayer coating.

  15. Dehydrochlorinated poly vinyl alcohol (PVA) films for food irradiation dosimeters

    International Nuclear Information System (INIS)

    Susilawati; Saion, E.B.; Doyan, A.; Lepit, A.; Wan Yusoff, W.M.D.

    2002-01-01

    Radiation sensitive dosimeters based on dyed poly vinyl alcohol (PVA) films containing chloral hydrate CCl 3 CH(OH) 2 and acid-sensitive cresol-red dye have been developed for use in food irradiation dosimetry. These polymer dosimeters undergo colour change from yellow (colour of basic form) to red (colour of acid form) upon exposure to gamma radiation. The radiation-induced change in colour was analysed using UV-Vis spectrometer. The absorption spectra produced two absorption modes, peaking at 438 nm for low doses and 529 nm for high doses. The dose-response was obtained by the changes in absorbance as a function of the absorbed dose. Results of the dose-response curves show the absorption decreases and increases experientially at modes 438 nm and 529 nm respectively with absorbed dose. The change in colour of the irradiated films was analysed using Raman spectrometer, which provides the spectra of molecular stretching modes of vibration of some chemical bonds in the films. The relative intensity at C-Cl stretching peaks of chloral hydrate decreases with absorbed dose and makes the films more acidic. Consequently the relative intensity at S-H and C=C stretching peaks of the dye increases with absorbed dose as the acid reacts with the dye and changes the structure and colour of the dye. (Author)

  16. Interaction between poly(vinyl pyridine) and poly(2,6-dimethyl-1,4-phenylene oxide) : A copolymer blend miscibility study

    NARCIS (Netherlands)

    de Wit, Joost; van Ekenstein, Gert Alberda; ten Brinke, Gerrit

    2007-01-01

    The phase behavior of blends of poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) with random copolymers of styrene and 2-vinyl pyridine, Poly(S-co-2VP), as well as with random copolymers of styrene and 4-vinyl pyridine, Poly(S-co-4VP), has been investigated in order to estimate the values of the

  17. Radiation crosslinking of polymer blends

    International Nuclear Information System (INIS)

    Spenadel, L.

    1979-01-01

    Rocked by the one-two punch of rising energy costs and tougher pollution controls, a growing number of companies are looking to radiation crosslinking as a cheaper, cleaner alternative to heat and costly chemical crosslinking agents such as peroxides. With the development of larger, more powerful electron beam machines it is now possible to irradiate parts as thick as 400 mils in a single pass. Two application areas which have been investigated at our laboratory are the electron beam processing of thermoplastic elastomeric automotive parts and EPDM electrical insulation. This paper covers work carried out to develop the necessary technology base for the radiation crosslinking of ethylene propylene/polyolefin blends. Initial results indicate that EP/PE blends of electrical insulation quality cross-link quite readily when irradiated. On the other hand, EP/PP blends developed for automotive fascia require the addition of crosslinking monomers such as trimethylol propane trimethacrylate in order for crosslinking to predominate over chain scission. Crosslinking EP/PP blends improve mar resistance, flexural set and deformation at elevated temperatures. These are all key properties for automotive fascia. (author)

  18. Ester Sensing with Poly (Aniline-co-m-aminobenzoic Acid Deposited on Poly (Vinyl Alcohol

    Directory of Open Access Journals (Sweden)

    S. ADHIKARI

    2011-02-01

    Full Text Available Poly (aniline-co-m-aminobenzoic acid was deposited on poly (vinyl alcohol film by in situ oxidative polymerization of the monomers aniline and m-aminobenzoic acid. Sensing experiments were performed on the composite film with the injection of various concentrations of hexenyl acetate and hexenyl butyrate at room temperature. The sensor responded rapidly and reversibly in the presence of hexenyl acetate and hexenyl butyrate vapors which was detected by resistance change of the composite film upon exposure to the vapor. Selectivity tests revealed that the sensor selectively responded to hexenyl butyrate compared to hexenyl acetate. The sensing response has been explained on the basis of FT-IR spectroscopic analysis of the polymer film before and after exposure to the ester vapor.

  19. Poly(vinyl alcohol)-heparin hydrogels as sensor catheter membranes

    NARCIS (Netherlands)

    Brinkman, E.; van der Does, L.; Bantjes, A.

    1991-01-01

    Poly(vinyl alcohol)-heparin hydrogels with varying water content were synthesized for use as sensor catheter membranes. Films were cast from aqueous mixtures of poly(viny) alcohol) (PVA), a photosensitive cross-linker p-diazonium diphenyl amine polymer (PA), glutaraldehyde (GA) and heparin. After

  20. Miscibility and Hydrogen Bonding in Blends of Poly(4-vinylphenol/Poly(vinyl methyl ketone

    Directory of Open Access Journals (Sweden)

    Hana Bourara

    2014-10-01

    Full Text Available The miscibility and phase behavior of poly(4-vinylphenol (PVPh with poly(vinyl methyl ketone (PVMK was investigated by differential scanning calorimetry (DSC, Fourier transform infrared spectroscopy (FTIR and scanning electron microscopy (SEM. It was shown that all blends of PVPh/PVMK are totally miscible. A DSC study showed the apparition of a single glass transition (Tg over their entire composition range. When the amount of PVPh exceeds 50% in blends, the obtained Tgs are found to be significantly higher than those observed for each individual component of the mixture, indicating that these blends are capable of forming interpolymer complexes. FTIR analysis revealed the existence of preferential specific interactions via hydrogen bonding between the hydroxyl and carbonyl groups, which intensified when the amount of PVPh was increased in blends. Furthermore, the quantitative FTIR study carried out for PVPh/PVMK blends was also performed for the vinylphenol (VPh and vinyl methyl ketone (VMK functional groups. These results were also established by scanning electron microscopy study (SEM.

  1. Influence of acrylonitrile butadiene rubber on recyclability of blends prepared from poly(vinyl chloride) and poly(methyl methacrylate).

    Science.gov (United States)

    Suresh, Sunil S; Mohanty, Smita; Nayak, Sanjay K

    2018-06-01

    The current investigation deals with the recycling possibilities of poly(vinyl chloride) and poly(methyl methacrylate) in the presence of acrylonitrile butadiene rubber. Recycled blends of poly(vinyl chloride)/poly(methyl methacrylate) are successfully formed from the plastic constituents, those are recovered from waste computer products. However, lower impact performance of the blend and lower stability of the poly(vinyl chloride) phase in the recycled blend restricts its further usage in industrial purposes. Therefore, effective utilisation acrylonitrile butadiene rubber in a recycled blend was considered for improving mechanical and thermal performance. Incorporation of acrylonitrile butadiene rubber resulted in the improvement in impact performance as well as elongation-at-break of the recycled blend. The optimum impact performance was found in the blend with 9 wt% acrylonitrile butadiene rubber, which shows 363% of enhancement as compared with its parent blend. Moreover, incorporated acrylonitrile butadiene rubber also stabilises the poly(vinyl chloride) phase present in the recycled blend, similarly Fourier transform infrared spectroscopy studies indicate the interactions of various functionalities present in the recycled blend and acrylonitrile butadiene rubber. In addition to this, thermogravimetric analysis indicates the improvement in the thermal stability of the recycled blend after the addition of acrylonitrile butadiene rubber into it. The existence of partial miscibility in the recycled blend was identified using differential scanning calorimetry and scanning electron microscopy.

  2. Development of functionalized hydroxyapatite/poly(vinyl alcohol) composites

    Science.gov (United States)

    Stipniece, Liga; Salma-Ancane, Kristine; Rjabovs, Vitalijs; Juhnevica, Inna; Turks, Maris; Narkevica, Inga; Berzina-Cimdina, Liga

    2016-06-01

    Based on the well-known pharmaceutical excipient potential of poly(vinyl alcohol) (PVA) and clinical success of hydroxyapatite (HAp), the objective of this work was to fabricate functionalized composite microgranules. PVA was modified with succinic anhydride to introduce carboxyl groups (-COOH), respectively, by reaction between the -OH groups of PVA and succinic anhydride, for attachment of drug molecules. For the first time, the functionalized composite microgranules containing HAp/PVA in the ratio of 1:1 were prepared through in situ precipitation of HAp in modified PVA aqueous solutions followed by spray drying of obtained suspensions. The microgranules were characterized by Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and differential scanning calorimetry (DSC). The presence of -COOH groups was verified by FT-IR, and the amount of functional groups added to PVA molecules (averaging 15 mol%) was determined by nuclear magnetic resonance spectroscopy (NMR). DSC results showed that modification with -COOH groups slightly decreased the thermal stability of PVA. FT-IR and XRD analysis confirmed that the resulting composites contain mainly nanocrystalline HAp and PVA. Moreover, the images taken by FE-SEM revealed that the microgranules consisted of nanosized HAp crystallites homogenously embedded in the PVA matrix. DSC measurements indicated that decomposition mechanism of the HAp/PVA differs from that of pure PVA and occurs at lower temperatures. However, the presence of HAp had minor influence on the thermal decomposition of the PVA modified with succinic anhydride. The investigation of composite microgranules confirmed interaction and integration between the HAp and PVA.

  3. Automobile parts by radiation crosslinking

    International Nuclear Information System (INIS)

    Yoshii, Fumio

    2008-01-01

    Radiation crosslinking, graft polymerization and degradation are useful technologies to improve polymer materials. The crosslinking causes improvement in strength, heat stability and processability to gives network structure for polymer materials and hence crosslinked materials are used in various fields, especially car parts. Electron beam (EB) of short time irradiation is used for these modifications. Irradiated (pre-vulcanized) before sulfur vulcanization rubber tires, heat resistant wires/cables, shrinkable tubes and foams of car parts are achieved by EB crosslinking. Polyethylene and polyvinyl chloride are used in cables and wires, polypropylene in plastic foams and natural rubber etc. In this paper radiation processing of tire, wire/cables, foams, shrinkable tubes and circuit protection devices (CPT) are explained. (author)

  4. Effect of various solvents on the viscosity-average molecular weight of poly (vinyl acetate)

    International Nuclear Information System (INIS)

    Rehman, W.U.; But, M.A.; Chughtai, A.; Jamil, T.; Sattar, A.

    2006-01-01

    Solution polymerization of Vinyl Acetate was carried out in various solvents (benzene, toluene, ethyl acetate, acetonitrile). Dilute solution viscometry was used to determine the viscosity-average molecular weight of the resulting Poly (Vinyl Acetate) (PV Ac) in each case. The viscosity-average molecular weight (M,J of PVAc was found to increase in the order benzene < toluene < ethyl acetate < acetonitrile, It was concluded that under the same reaction conditions (polymerization time, initiator quantity, solvent/monomer ratio, temperature), acetonitrile served as the best solvent for solution. polymerization of Vinyl Acetate monomer. (author)

  5. Preparation, Characterization and Permeation Behavior of Poly(methyl acrylate-Poly(dimethyl siloxane-Poly(methyl acrylate Block Copolymer/Poly(vinyl acetate Blend Membranes

    Directory of Open Access Journals (Sweden)

    Mohammad Ali Semsarzadeh

    2015-03-01

    Full Text Available Structure of polymeric materials is of the most important factors in determination of the characteristics and properties of the membranes. Various research and developments on polymeric membranes confirm the direct correlation between structure-properties of polymeric membranes. In this research, the structural outcome of poly(methyl acrylate-poly(dimethyl siloxane-poly(methyl acrylate/poly(vinyl acetate blend membranes and its relationship with gas permeation behavior of the blends were investigated. The flexible block copolymer of poly(methyl acrylate-poly(dimethyl siloxane-poly(methyl acrylate (PMA-PDMS-PMA was synthesized via atom transfer radical polymerization. Morphology and chemical structure of the synthesized block copolymer was investigated by Fourier transform infrared spectroscopy, proton nuclear magnetic resonance, gel permeation chromatography, X-ray diffraction analysis, differential scanning calorimetry and scanning electron microscopy. Blend membranes of PMA-PDMS-PMA and poly(vinyl acetate (PVAc were prepared by solution casting method in different compositions. By adding poly(vinyl acetate to PMA-PDMS-PMA block copolymer, the selectivity of the membranes for carbon dioxide/methane pair gases were increased by 55%. Fractional free volume (an indication of chain packing efficiency in blend membranes and dielectric constant (an indication of the molar volume and molar polarization of the blend membranes were obtained as the factors reflected the microstructural effect of PMA-PDMS-PMA and PVAc blend membranes. The efforts were directed toward expressing more precise structure-properties relationship of PMA-PDMS-PMA/PVAc blend membranes. The experimental permeability values of the blend membranes reported in this research were compared with the modified logarithmic model. The modified logarithmic model was evaluated for other blend membranes.

  6. Poly/vinyl alcohol/ membranes for reverse osmosis

    Science.gov (United States)

    Katz, M. G.; Wydeven, T., Jr.

    1981-01-01

    A description is presented of the results of studies of the water and salt transport properties of PVA membranes, taking into account radiation crosslinked PVA membranes, diffusive salt permeability through PVA membranes, and heat treated PVA membranes. The experimental findings support an occurrence of independent water, and salt permeation processes. It is suggested that the salt permeation is governed by a solution-diffusion transport mechanism. The preparation of thin skinned, asymmetric PVA membranes is also discussed. The employed method has a certain similarity to the classical phase inversion method, which is widely applied in the casting of asymmetric reverse osmosis membranes. Instead of using a gelling bath composed of a nonsolvent for the membrane material and miscible with the solvent from which the membrane is cast, a 'complexing' bath is used, which is a solution of a complexing agent in water.

  7. Rheological properties of poly-vinyl-chloride solutions in varioussolvents

    International Nuclear Information System (INIS)

    Kurbanaliev, M.K.; Narzullaev, B.N.; Dustov, I.K.; Marupov, R.M.

    1976-01-01

    The present article is the result of studying of curves process ofpoly-vinyl-chloride solutions in wide interval of tension and velocities ofshear in thermodynamically good and bad solvents at various temperatures

  8. Preparation and characterization of film of poly vinyl acetate ethylene copolymer emulsion

    International Nuclear Information System (INIS)

    Zhang, Yanhua; Gu, Jiyou; Tan, Haiyan; Shi, Junyou; Di, Mingwei; Zuo, Yingfeng; Qiu, Si

    2013-01-01

    In order to improve the storage modulus and water resistance of poly (vinyl acetate), the vinyl acetate and poly (vinyl alcohol) (PVA) were respectively used as monomers and protective colloid to prepare a new kind of polyvinyl acetate emulsion adhesive by continuous emulsion polymerization. The dynamic mechanics, particle distribution, glass transition temperature, polymer emulsion structure of both polymerized and copolymerized emulsion were analyzed by SEM, DMA and XPS, respectively. The results indicated that the copolymerized emulsion has the appropriate particle size and the uniform particle distribution, the glass transition temperature increased from 50 °C to 70 °C, compared with poly (vinyl acetate). It could be seen from XPS spectra of copolymerized emulsion that key characteristic peak of C=O was still existent. X-ray photoelectron spectra revealed that the addition of EVA did not generate the new bond, whereas the maximum percentage increases in ester was determined in the composite film with the introduction of EVA of 25%, which indicated that the composite film has copolymer structure. The storage modulus and water resistance of poly (vinyl acetate) were improved due to the introduction of the EVA.

  9. A Model Approach for Finding Cleaning Solutions for Plasticized Poly(Vinyl Chloride) Surfaces of Collections Objects

    DEFF Research Database (Denmark)

    Sanz Landaluze, Jon; Egsgaard, Helge; Morales Munoz, Clara

    2014-01-01

    This study focused on developing a surface cleaning treatment for one type of commercially available plasticized poly(vinyl chloride). The effects of cleaning solutions on samples of plasticized poly(vinyl chloride) were examined by several methods. The sample surface, prior to and after artifici...

  10. Preparation and characterization of poly(vinyl sulfone)- and poly(vinylidene fluoride)-based electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Choe, H.S.; Giaccai, J.; Alamgir, M.; Abraham, K.M. [EIC Labs., Inc., Norwood, MA (United States)

    1995-10-01

    A novel group of polymer electrolytes based on poly(vinyl sulfone) (PVS) and poly(vinylidene fluoride) (PVdF) polymers, plasticized with highly conductive solutions of LiClO{sub 4}, LiN(CF{sub 3}SO{sub 2}){sub 2} or LiAsF{sub 6} dissolved in ethylene carbonate, propylene carbonate, sulfolane, or mixtures thereof, was prepared via in situ photopolymerization and solution casting, respectively. The polymer electrolytes were characterized from conductivity and cyclic voltammetry data. It was found that solutions of Li salts in the vinyl sulfone monomer were highly conductive at room temperature with conductivities of 0.6 to 1.3 x 10{sup -3} {Omega}{sup -1}cm{sup -1} at 30{sup o}C, but the conductivities decreased by about 10{sup 3} times on polymerizing. Conversely, the conductivities increased by about 10{sup 2} to 10{sup 4} times on incorporating plasticizing solvents into the solid polymer electrolytes, suggesting that ionic mobility is the primary factor affecting the conductivities of solid polymer electrolytes. The highest conductivity exhibited by PVS-based electrolyte was 3.74 x 10{sup -4} {Omega}{sup -1}cm{sup -1} and that by PVdF-based electrolyte was 1.74 x 10{sup -3} {Omega}{sup -1}cm{sup -1}, at 30{sup o}C. The PVS-based electrolytes were found to be stable to oxidation up to potentials ranging between 4.5 and 4.8 V, while the stable potential limits for PVdF-based electrolytes were between 3.9 and 4.3 V vs. Li{sup +}/Li. (author)

  11. The response of poly (vinyl alcohol) to humidity

    International Nuclear Information System (INIS)

    Spindura, J.

    2000-01-01

    This thesis aims to investigate the effects of heat treatments, humidity and hydrogen bonding on thin film and fibre samples of poly (vinyl alcohol). A number of different techniques are utilised in order to analyse samples that have undergone a number of different treatments. The techniques include X-ray diffraction (XRD), differential scanning calorimetry (DSC), and dynamic mechanical analysis (DMA). From the XRD and DSC work the increase in crystallisation due to annealing time and temperature has been investigated and for dry samples the crystallinity was found to be dependant on both the temperature and also the heating method. For samples exposed to varying humidities and annealed in this wet environment two stages of crystallisation have been proposed. The crystals formed are of two types, those with small unit cell parameters and low melting points, and a second class of crystals with bigger unit cell parameters which, perhaps surprisingly, were found to have the higher melting points. The melting temperature was also not found to be significantly dependant on the amount of water take up or the degree of crystallinity. These changes have been explained in terms of the hydrogen bonding between the polymer chains and between the polymer and water molecules. Solubility and swelling experiments showed that as the crystallinity of the sample increases the amount of water the sample is able to absorb is reduced. This is because it is the amorphous region of the material that swells, although it has been shown that not all the amorphous material swells to the same extent. The glass transition temperature (T g ) could not be followed with DSC as the semicrystalline nature of the samples masked this transition and hence DMA was used to follow the changes in T g with both annealing and moisture content. A decrease in T g with increasing humidity was clearly observed. An interesting observation was the increase in T g for films exposed to humidity and then dried

  12. Synthesis and rheological properties of poly(vinyl alcohol)

    International Nuclear Information System (INIS)

    Lee, Jung Kyung; Lee, Hyang Aee; Kim, Keyng Yi

    2001-01-01

    Vinyl acetate usually used in PVA resin preparation was converted to PVAc by bulk poly-merization using AIBN as a initiator and PVA was synthesized by changing the concentration of NaOH added for saponification subsequently. As a result of estimating molecular weight using GPC, molecular weight increased as the NaOH concentration increased to 2.5 N, 5.0 N, 7.5 N and 10.0 N and polydispersity had similar values of 2.1∼2.3, however, showed slightly decreasing tendency. In addition, PVA saponificated by 10.0 N-NaOH showed high syndiotacticity in observation of tacticity using NMR spectroscopy. From this fact, the degree of tacticity was predicted to be high and it was in good agreement with the tendency of polydisperisity by GPC. Also, from the result of FT-IR spectroscopy, it might be known that hydrolysis was more promoted in the PVA with 10.0 N-NaOH than other NaOH concentration. Intrinsic viscosity measured using Ubbelohde viscometer, which increased as the concentration of NaOH added for saponification increased. The change of shear strength with the change of shear rate was investigated using Brookfield viscometer, in consequence, viscosity of PVA synthesized decreased as shear rate increased. PVA solution confirmed to show the shear thinning behavior by Casson plot and PVA with 10.0 N-NaOH had the largest yield value. DSC measurement was performed to know the thermal properties of PVA. Tp had nearly constant value of 214 .deg. C in all cases except for adding 2.5 N-NaOH and ΔH was increased as the concentration of NaOH increased. From this properties, it was concluded that the degree of hydrogen bonding was proportional to the added concentration of NaOH and the increase of the degree of hydrogen bonding and hydrophobic interaction could affect the rheological and thermal properties of title compound

  13. EB radiation crosslinking of elastomers

    International Nuclear Information System (INIS)

    Bik, J.; Rzymski, M.; Gluszewski, W.; Zagorski, Z.P.

    2002-01-01

    Complete text of publication follows. The first paper in the series described by the general title, starts with radiation crosslinking of hydrogenated butadiene-nitrile rubber (HBNR). This high-tech elastomer is obtained by catalytic hydrogenation of >C=C 99.5 and 94.5% of starting double bonds. Samples were irradiated with 10 MeV electrons, monoenergetical, 6 kW power, used as scanned beam over the conveyor, securing homogeneity of dose distribution. The doses were up to 300 kGy, applied in 20 kGy increments to avoid radiation generated heating of the material. The influence of presence or absence of oxygen was considered. Irradiated samples were investigated for the extend of crosslinking in the function of dose and for properties important for understanding of mechanisms. Samples are transparent, what allowed conventional absorption spectrophotometry, also time resolved. The quantitative interpretation of results shows that for 100 crosslinks there are 6-9 acts of chain-scission. It is less, than expected from the participation of multi-ionization spurs, also in the solid state, as announced during the previous, 9th Tihany Conference. However, the apparent lower yield of multi-ionization spurs is explained by partial conversion of products into crosslinks of specific type. Our investigations confirm the usefulness of consideration of radiation spurs in polymers as well as in all, low LET irradiated media

  14. Preparation of various hydrogels based on poly (Vinyl pyrrolidone) and poly ethylene glycol using gamma and electron irradiation

    International Nuclear Information System (INIS)

    Ajji, Z.

    2006-11-01

    Different hydrogels have been prepared using gamma and electron irradiation; the hydrogels are composed of poly(vinyl pyrolidone) (PVP), poly(ethylene glycol) (PEG). The influence of some process parameters on the properties of the hydrogels has been investigated as: the gel fraction, maximum swelling, swelling kinetics, and mechanical properties. In the first part of this study, hydrogel dressings have been prepared using electron irradiation, and the dressings are composed of poly(vinyl pyrrolidone) (PVP), poly(ethylene glycol) (PEG) and agar. The gel fraction increases with increasing PVP concentration due to increased crosslink density, and decreases with increasing the PEG concentration. PEG seems to act not only as plasticizer but also to modify the gel properties as gelation% and maximum swelling. The prepared hydrogels dressings could be considered as a good barrier against microbes. In the second part, different hydrogels have been prepared based on different concentrations of poly(vinyl pyrrolidone) and using gamma irradiation. The gel fraction and maximum swelling of the hydrogels has been determined. In the third part of the study, different hydrogels have been prepared based on different concentrations of poly(vinyl pyrrolidone) and poly(ethylene glycol) (PEG) with various molecular weights, and using gamma irradiation. The gel fraction and maximum swelling of the hydrogels has been determined. The data show that PEG with low molecular weight needs a high dose for the gelation, and the presence of PVP lowers the needed gelation dose. The maximum swelling decreases with increasing irradiation dose and the PVP concentration, which is due to higher crosslinks between the polymer chains. (author)

  15. Effect of gamma ray on poly(lactic acid)/poly(vinyl acetate-co-vinyl alcohol) blends as biodegradable food packaging films

    International Nuclear Information System (INIS)

    Razavi, Seyed Mohammad; Dadbin, Susan; Frounchi, Masoud

    2014-01-01

    Poly(lactic acid) (PLA)/poly(vinyl acetate-co-vinyl alcohol) [P(VAc-co-VA)] blends as new transparent film packaging materials were prepared at various blend compositions and different vinyl alcohol contents. The blends and pure PLA were irradiated by gamma rays to investigate the extent of changes in the packaging material during gamma ray sterilization process. The miscibility of the blends was dependent on the blend composition and vinyl alcohol content; gamma irradiation had little effect on the extent of miscibility. The glass transition temperature of pure PLA and PLA/P(VAc-co-VA) miscible blends reduced after irradiation. On the other hand in PLA/P(VAc-co-VA) immiscible blends, while the glass transition temperature of the PLA phase decreased; that of the copolymer phase slightly increased. The reduction in the glass transition was about 10 percent for samples irradiated with 50 kGy indicating dominance of chain scission of PLA molecules at high irradiation dose. The latter was verified by drop in mechanical properties of pure PLA after exposing to gamma irradiation at 50 kGy. Blending of PLA with the copolymer P(VAc-co-VA) compensated greatly the adverse effects of irradiation on PLA. The oxygen-barrier property of the blend was superior to the neat PLA and remained almost intact with irradiation. The un-irradiated and irradiated blends had excellent transparency. Gamma ray doses used for sterilization purposes are usually less than 20 kGy. It was shown that gamma irradiation at 20 kGy had no or little adverse effects on PLA/P(VAc-co-VA) blends mechanical and gas barrier properties. - Highlights: • Poly(lactic acid)/poly(vinyl acetate-co-vinyl alcohol) blends were prepared as new packaging film. • The blends are superior to PLA in oxygen gas barrier property. • The blends are suitable for gamma ray sterilization and maintain useful mechanical properties. • The blends are perfectly transparent

  16. Structure of chlorinated poly(vinyl chloride). III. Preparation of poly(vinyl chloride)-β,β-d2 as a model for the study of the mechanism of chlorination and of the chlorinated poly(vinyl chloride) structure

    International Nuclear Information System (INIS)

    Lukas, R.; Kolinsky, M.

    1976-01-01

    A method for the preparation of poly(vinyl chloride)-β,β-d 2 (PVC-β,β-d 2 ) as a model for the investigation of the mechanism of chlorination and of the CPVC structure has been suggested. The conditions of preparation of deuterated intermediates of a multistage synthesis of vinyl chloride-β,β-d 2 and of suspension-polymerized PVC-β,β-d 2 have been described including the mass balance. Malonic acid was used as the starting compound. Tacticity values of a sample of PVC-β,β-d 2 and its infrared and nuclear magnetic resonance (NMR) spectra are presented and compared with the data already published

  17. Elution behavior of poly(ethylene glycol) through poly(vinyl alcohol) gel column using several solvents as eluents

    International Nuclear Information System (INIS)

    Hirayama, Chuichi; Motozato, Yoshiaki; Matsumoto, Kazuaki.

    1983-01-01

    γ-Irradiated poly(vinyl alcohol) beads, which were sufficiently allowed to swell in water, were washed with methanol, and then were packed into column. Gel chromatography was performed using methanol, benzene, esters and ketones as eluents and poly(ethylene glycol) as a sample. When the elution was carried out using methanol and benzene as eluents, elution behavior of samples was ordinary. When ethyl formate, methyl acetate and ethyl propionate were used as eluents, samples were slightly adsorbed and the elution was delayed. In the case the elution was carried out using ethyl acetate, propyl acetate, butyl acetate and ethyl methyl ketone as eluents, samples were adsorbed strongly on the bed material, and the adsorption curve was analogous to the calibration curve using methanol as an eluent. Dried poly(vinyl alcohol) gel as a packing material, showed ordinary elution behaviors for the samples. The adsorption of poly(ethylene glycol) on the present bed material was attributed to the existence of hydrated water on poly(vinyl alcohol) gel matrix. (author)

  18. Biaxial stress-strain behavior of chemical and physical gels of poly(vinyl alcohol)

    Czech Academy of Sciences Publication Activity Database

    Meissner, Bohumil; Matějka, Libor

    2008-01-01

    Roč. 49, č. 10 (2008), s. 2560-2567 ISSN 0032-3861 R&D Projects: GA AV ČR IAA400500701 Institutional research plan: CEZ:AV0Z40500505 Keywords : poly(vinyl alcohol) gels * pure shear behavior * constitutive equation Subject RIV: CD - Macromolecular Chemistry Impact factor: 3.331, year: 2008

  19. Microstructure and molecular interaction in glycerol plasticized chitosan/poly(vinyl alcohol) blending films

    Science.gov (United States)

    Poly (vinyl alcohol) (PVA)/chitosan (CS) blended films plasticized by glycerol were investigated using mechanical testing, atomic force microscopy (AFM), differential scanning calorimetry (DSC) and FTIR spectroscopy, with primary emphasis on the effects of the glycerol content and the molecular weig...

  20. Inhibiting the deterioration of plasticised poly (vinyl chloride) in museum collections

    DEFF Research Database (Denmark)

    Shashoua, Yvonne

    2003-01-01

    Plasticized poly (vinyl chloride) (PVC) is found in museum collections as three dimensional objects and as packaging materials. Many PVC materials deteriorate within 25 years of acquisition. Migration and chemical breakdown of plasticizer, accompanied by dehydrochlorination of the polymer are the...

  1. Additive effects on phase transition and interactions in poly(vinyl methyl ether) solutions

    Czech Academy of Sciences Publication Activity Database

    Starovoytova, Larisa; Šťastná, J.; Šturcová, Adriana; Konefal, Rafal; Dybal, Jiří; Velychkivska, Nadiia; Radecki, M.; Hanyková, L.

    2015-01-01

    Roč. 7, č. 12 (2015), s. 2572-2583 ISSN 2073-4360 R&D Projects: GA ČR(CZ) GA13-23392S Institutional support: RVO:61389013 Keywords : additives * LCST * poly(vinyl methyl ether) Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 2.944, year: 2015

  2. Preparation of CuS nanoparticles embedded in poly(vinyl alcohol ...

    Indian Academy of Sciences (India)

    WINTEC

    ray diffraction (XRD) analyses and electron diffraction pattern also revealed the forming of CuS crystal structure in the PVA fibres. Keywords. CuS nanoparticles; electrospinning; poly(vinyl alcohol). 1. Introduction. In the past decade, the preparation of low-dimensional semiconductor nanostructures has become a hotspot of.

  3. Terpyridine modified poly(vinyl chloride) : possibilities for supramolecular grafting and crosslinking

    NARCIS (Netherlands)

    Meier, M.A.R.; Schubert, U.S.

    2003-01-01

    Commercially available poly(vinyl chloride) (PVC) was covalently modified with terpyridine supramolecular binding units in a two-step reaction. First, PVC was modified with aromatic thiols to introduce OH functionalities into the polymer backbone, which were subsequently reacted with an

  4. The influence of stretching on tensile strength and solubility of poly(vinyl alcohol) fibres

    NARCIS (Netherlands)

    Heikens, D.; Bleijenberg, A.C.A.M.; Hoppenbrouwers, J.J.M.; Barentsen, W.M.

    1971-01-01

    The strength of wet-spun poly(vinyl alcohol) (pva) fibres is given as function of bath-stretching, wet-stretching and hot-stretching. In the two equations derived for strength of wet-stretching and hot-stretching the complex influence of the bath-stretching and hot-stretching is demonstrated. The

  5. Effects of solvents on the radiation grafting reaction of vinyl compounds on poly (3-hydroxybutyrate)

    International Nuclear Information System (INIS)

    Torres, Maykel González; Talavera, José Rogelio Rodríguez; Muñoz, Susana Vargas; Pérez, Manuel González; Castro, Ma. Pilar. Carreón.; Cortes, Jorge Cerna

    2015-01-01

    Vinyl Acetate was grafted onto poly (3-hydroxybutyrate) by the simultaneous gamma irradiation method using different types of solvents and in bulk (solvent free), at 10 kGy and 1.62 kGy/h dose and dose rate respectively. Subsequent complete hydrolysis allowed the conversion of grafted chains from poly (vinyl acetate) to poly (vinyl alcohol). The aim of this study is to determine the effect of solvent through the estimation of the dependence of the degree of grafting with the choice of solvent, the calculation of the degree of crystallinity, and to study the biodegradation of the products. The results showed a greater degree of grafting in bulk, while the more suitable solvent was hexane. Characterization of the grafted copolymer indicated that crystallinity percentage decreased by an increase in grafting, while the biodegradability was promoted by the increment in poly (vinyl alcohol) grafted. - Highlights: • PHB was indirectly grafted with PVA, by complete hydrolysis of grafted PVAc. • The effect of solvents on the grafting, crystallinity and biodegradation was studied. • The characterizations of the products were obtained by SEM, TGA, and DSC

  6. Influence of polymer chain architecture of poly(vinyl alcohol) on the inhibition of ice recrystallization

    NARCIS (Netherlands)

    Olijve, L.L.C.; Hendrix, M.M.R.M.; Voets, I.K.

    2016-01-01

    Poly(vinyl alcohol) (PVA) is a water-soluble synthetic polymer well-known to effectively block the recrystallization of ice. The effect of polymer chain architecture on the ice recrystallization inhibition (IRI) by PVA remains unexplored. In this work, the synthesis of PVA molecular bottlebrushes is

  7. Disk Refining and Ultrasonication Treated Sugarcane Bagasse Residues for Poly(Vinyl Alcohol) Bio-composites

    Science.gov (United States)

    Qingzheng Cheng; Zhaohui Tong; Luisa Dempere; Lonnie Ingram; Letian Wang; J.Y. Zhu

    2013-01-01

    Disk refining and ultrasonication treated sugarcane bagasse residues reclaimed from the waste stream of a simplified bioethanol process after fermentation were used to fabricate biobased composites with poly(vinyl alcohol) (PVA) by film casting. The morphologies and the size distributions of residue particles were characterized by scanning electronic microscopy and...

  8. Modeling of the Migration of Glycerol Monoester Plasticizers in Highly Plasticized Poly(vinyl chloride)

    DEFF Research Database (Denmark)

    Lundsgaard, Rasmus; Kontogeorgis, Georgios; Kristiansen, Jørgen K.

    2009-01-01

    soybean oil (ESBO) with regard to their migration from three different types of poly(vinyl chloride) into isooctane at 20, 40, and 60 degrees C. Diffusion coefficients derived from the experimental migration data were evaluated against diffusion coefficients estimated from a model based solely...

  9. Preparation of CuS nanoparticles embedded in poly(vinyl alcohol)

    Indian Academy of Sciences (India)

    Poly(vinyl alcohol) (PVA)/CuS composite nanofibres were successfully prepared by electrospinning technique and gas–solid reaction. Scanning electron microscopic (SEM) images showed that the average diameter of PVA/CuS fibres was about 150–200 nm. Transmission electron microscopy (TEM) proved that a majority ...

  10. Fracture behavior of highly toughened poly(lactic acid)/ethylene-co-vinyl acetate blends

    NARCIS (Netherlands)

    Zeng, Q.; Feng, Y.; Wang, R.; Ma, P.

    2018-01-01

    Poly(lactic acid) (PLA) is brittle which restricts the range of its applications. The toughness of PLA was effectively improved in this work by incorporation of rubber grade ethylene-co-vinyl acetate (EVM). For example, the elongation at break of PLA increased by about 50 times after the addition of

  11. Poly(vinyl-alcohol)/poly(ethylene-glycol)/poly(ethylene-imine) blend membranes - structure and CO2 facilitated transport

    International Nuclear Information System (INIS)

    Ben Hamouda, S.; Quang, Trong Nguyen; Langevin, D.; Sadok, Roudeslic

    2010-01-01

    Poly(vinyl-alcohol) (PVA)/poly(ethylene-imine) (PEI)/poly(ethylene-glycol) (PEG) blend membranes were prepared by solution casting followed by solvent evaporation. The effects of the blend polymer composition on the membrane structure and CO 2 /N 2 permeation characteristics were investigated. IR spectroscopy evidenced strong hydrogen bonding interactions between amorphous PVA and PEI, and weaker interactions between PVA and PEG. DSC studies showed that PVA crystallization was partially inhibited by the interactions between amorphous PVA and PEI blend, in which PEG separated into nodules. The CO 2 permeability decreased with an increase in CO 2 partial pressure in feed gas, while the N 2 permeability remained constant. This result indicated that only CO 2 was transported by the facilitated transport mechanism. The CO 2 and N 2 permeabilities increased monotonically with the PEI content in the blend membranes, whereas the ideal selectivity of CO 2 to N 2 transport showed a maximum. When CO 2 is humidified, its permeability through the blend membranes is much higher than that of dry CO 2 , but the change in permeability due to the presence of humidity is reversible. (authors)

  12. Electrodialytic Transport Properties of Anion-Exchange Membranes Prepared from Poly(vinyl alcohol) and Poly(vinyl alcohol-co-methacryloyl aminopropyl trimethyl ammonium chloride).

    Science.gov (United States)

    Jikihara, Atsushi; Ohashi, Reina; Kakihana, Yuriko; Higa, Mitsuru; Kobayashi, Kenichi

    2013-01-02

    Random-type anion-exchange membranes (AEMs) have been prepared by blending poly(vinyl alcohol) (PVA) and the random copolymer-type polycation, poly(vinyl alcohol-co-methacryloyl aminopropyl trimethyl ammonium chloride) at various molar percentages of anion-exchange groups to vinyl alcohol groups, Cpc, and by cross-linking the PVA chains with glutaraldehyde (GA) solution at various GA concentrations, CGA. The characteristics of the random-type AEMs were compared with blend-type AEMs prepared in our previous study. At equal molar percentages of the anion exchange groups, the water content of the random-type AEMs was lower than that of the blend-type AEMs. The effective charge density of the random-type AEMs increased with increasing Cpc and reached a maximum value. Further, the maximum value of the effective charge density increased with increasing CGA. The maximum value of the effective charge density, 0.42 mol/dm3, was obtained for the random-type AEM with Cpc = 4.2 mol % and CGA = 0.15 vol %. A comparison of the random-type and blend-type AEMs with almost the same Cpc showed that the random-type AEMs had lower membrane resistance than the blend-type ones. The membrane resistance and dynamic transport number of the random-type AEM with Cpc = 6.0 mol % and CGA = 0.15 vol % were 4.8 Ω cm2 and 0.83, respectively.

  13. Tailor-made starch-based conjugates containing well-defined poly(vinyl acetate and its derivative poly(vinyl alcohol

    Directory of Open Access Journals (Sweden)

    2011-06-01

    Full Text Available Reversible addition-fragmentation chain transfer (RAFT polymerization was adopted to synthesize starch-based conjugates that possessed controllable architecture and properties. Starch-based xanthate agent was prepared and applied as chain transfer agent to conduct the living/controlled polymerization (LCP of vinyl acetate, which generated tailor-made conjugates of starch and well-defined poly(vinyl acetate (SVAc. The relevant derivatives, conjugates of starch and chain length-controlled poly(vinyl alcohol (SVA, were obtained subsequently. Various characterizations such as Fourier transform infrared spectra (FTIR, ultraviolet-visible spectroscopy (UV, proton nuclear magnetic resonance (1H NMR, gel permeation chromatography (GPC, X-ray diffraction (XRD, Thermogravimetric analysis (TGA, and dynamic mechanical thermal analysis (DMTA were performed to examine the structure of intermediates and the starch-based conjugates. Static contact angle measurements revealed that the hydrophilic character of starch-based conjugates was tunable. Well-defined SVAc was amphiphilic and it was able to self-assemble into size controllable micelles, which was verified by contact angles, transmission electron microscopy (TEM and dynamic light scattering (DLS tests. SVA exhibited much higher capability to form physically cross-linked hydrogel than starch did. Both the characteristic of SVAc and SVA were chain length-dependent.

  14. Biomaterial properties evaluation of poly(vinyl acetate- alt-maleic anhydride)/chitosan nanocapsules

    Science.gov (United States)

    Raţă, Delia Mihaela; Popa, Marcel; Chailan, Jean-François; Zamfir, Carmen Lăcrămioara; Peptu, Cătălina Anişoara

    2014-08-01

    Nanocapsules with diameter around 100 nm based on a natural polymer (chitosan) and a synthetic polymer poly(vinyl acetate- alt-maleic anhydride) [poly(MAVA)] by interfacial condensation method were prepared. The present study proposes a new type of biocompatible nanocapsules based on poly(vinyl acetate- alt-maleic anhydride-chitosan) (MCS) able to become a reliable support for inclusion and release of drugs. The spherical shape of the nanocapsules was evidenced by scanning electron microscopy. Nanocapsules presented a good Norfloxacin loading and release capacity. Haemocompatibility tests have demonstrated that the nanocapsules present a low toxicity and a good compatibility with sanguine medium. The biocompatibility properties of the nanocapsules after their intraperitoneal administration in rats were evidenced by histopathological examination of different organs (brain, liver, kidney, and lung). The results are encouraging and the nanocapsules can be used as controlled drug delivery systems.

  15. Poly(Dimethylsiloxane)-Poly(Vinyl Alcohol) Coated Solid Phase Micro extraction Fiber for Chloropyrifos Analysis

    International Nuclear Information System (INIS)

    Wan Aini Wan Ibrahim; Nor Fairul Zukry Ahmad Rasdy; Norfazilah Muhamad

    2016-01-01

    Traditional liquid - liquid extraction of pesticides consumes large volumes of organic solvent which are hazardous to the operator and is not environment friendly. Solid phase micro extraction (SPME) is a solvent less extraction method which is safer to the operator and is environmental friendly. A sol-gel hybrid fibre coating material, poly(dimethylsiloxane)-poly(vinyl alcohol) (PDMS-PVA) was synthesized and used in head space solid phase micro extraction (HS-SPME) of chloropyrifos. The thickness of the synthesised PDMS-PVA fiber coating was 13.5 μm and it is thermally stable up to 400 degree Celsius. The PDMS-PVA sol-gel hybrid fiber was also stable to two organic solvents tested; acetonitrile and dichloromethane (1 hour dipping) and showed no significant changes in extraction performance for chloropyrifos. Extracted chloropyrifos was analysed using gas chromatography electron capture detector (GC-ECD). Optimum SPME parameters affecting the PDMS-PVA HS-SPME performance namely extraction time (15 min), extraction temperature (50 degree Celsius), desorption time (5 min), desorption temperature (260 degree Celsius) and stirring rate (120 rpm) were used for extraction. It was found that HSSPME using PDMS-PVA sol-gel fiber gave significantly better extraction performance of chloropyrifos compared to commercial 100 μm PDMS fiber. The PDMS-PVA fiber showed excellent operational performances such as temperature stability (up to 380 degree Celsius), coating lifetime (up to 170 times use) and organic solvent stability. The PDMS-PVA-HS-SPME method showed excellent recovery for chloropyrifos from tomatoes (98.0 %, 5.9 % RSD) at 0.01 μg/ g spiked level (5 times lower than maximum residue limit set by European Union). (author)

  16. Effect of gamma ray on poly(lactic acid)/poly(vinyl acetate-co-vinyl alcohol) blends as biodegradable food packaging films

    Science.gov (United States)

    Razavi, Seyed Mohammad; Dadbin, Susan; Frounchi, Masoud

    2014-03-01

    Poly(lactic acid) (PLA)/poly(vinyl acetate-co-vinyl alcohol) [P(VAc-co-VA)] blends as new transparent film packaging materials were prepared at various blend compositions and different vinyl alcohol contents. The blends and pure PLA were irradiated by gamma rays to investigate the extent of changes in the packaging material during gamma ray sterilization process. The miscibility of the blends was dependent on the blend composition and vinyl alcohol content; gamma irradiation had little effect on the extent of miscibility. The glass transition temperature of pure PLA and PLA/P(VAc-co-VA) miscible blends reduced after irradiation. On the other hand in PLA/P(VAc-co-VA) immiscible blends, while the glass transition temperature of the PLA phase decreased; that of the copolymer phase slightly increased. The reduction in the glass transition was about 10 percent for samples irradiated with 50 kGy indicating dominance of chain scission of PLA molecules at high irradiation dose. The latter was verified by drop in mechanical properties of pure PLA after exposing to gamma irradiation at 50 kGy. Blending of PLA with the copolymer P(VAc-co-VA) compensated greatly the adverse effects of irradiation on PLA. The oxygen-barrier property of the blend was superior to the neat PLA and remained almost intact with irradiation. The un-irradiated and irradiated blends had excellent transparency. Gamma ray doses used for sterilization purposes are usually less than 20 kGy. It was shown that gamma irradiation at 20 kGy had no or little adverse effects on PLA/P(VAc-co-VA) blends mechanical and gas barrier properties.

  17. Morphological, dielectric and electric conductivity characteristics of clay-containing nanohybrids of Poly(N-Vinyl Carbazole) and Polypyrrole

    CSIR Research Space (South Africa)

    Haldar, I

    2012-10-01

    Full Text Available Poly(N-vinyl carbazole) (PNVC) and polypyrrole (PPY)-montmorillonite (MMT) clay hybrids were prepared by mechanical grinding of the respective monomers with MMT followed by subsequent standard processing methods. Fourier transform infrared...

  18. Crystallisation of hydroxyapatite in phosphorylated poly(vinyl alcohol) as a synthetic route to tough mechanical hybrid materials

    Energy Technology Data Exchange (ETDEWEB)

    Kusakabe, Akane; Hirota, Ken; Mizutani, Tadashi, E-mail: tmizutan@mail.doshisha.ac.jp

    2017-01-01

    Partially phosphorylated poly(vinyl alcohol) was prepared by treating poly(vinyl alcohol) with 100% phosphoric acid, and 5, 10 and 20% of the hydroxyl groups were converted to phosphoric acid ester. Addition of Ca{sup 2+} to an aqueous solution of phosphorylated poly(vinyl alcohol) gave a transparent gel. Five cycles of alternate soaking of the gel in aqueous CaCl{sub 2} and aqueous (NH{sub 4}){sub 2}HPO{sub 4} were carried out to crystallise hydroxyapatite (HAP) in the phosphorylated poly(vinyl alcohol) matrix. The X-ray diffraction peaks of HAP formed in 5% phosphorylated PVA were sharp, while those of HAP formed in 20% phosphorylated PVA were broad. The contents of inorganic phase in the hybrid powder were increased from 58 to 76 wt% as the fraction of phosphate groups in the gel was decreased from 20% to 5%. The hybrid powder was first subjected to uniaxial pressing, followed by cold isostatic pressing (CIP) and warm isostatic pressing (WIP) at 120 °C at pressures of 300–980 MPa, to obtain the specimens for three-point bending test. These hybrid specimens showed bending strengths of 15–53 MPa. The hybrid compacts prepared from 10% phosphorylated poly(vinyl alcohol) showed the smallest Young's modulus, the largest displacement at break, and the largest fracture energy, showing that it has the highest toughness among the hybrid materials prepared from poly(vinyl alcohol) with varying degrees of phosphorylation. - Graphical abstract: Densification of hydroxyapatite crystallised in 10% phosphorylated poly(vinyl alcohol) gave the toughest compact. - Highlights: • Hydroxyapatite was crystallised in phosphorylated poly(vinyl alcohol) gels. • Crystallite size of hydroxyapatite decreased as phosphate density was increased. • The hybrid specimens prepared in 10% phosphorylated gel was the toughest. • Phosphate density in organic matrix regulated the mechanical properties of the hybrid.

  19. Crystallisation of hydroxyapatite in phosphorylated poly(vinyl alcohol) as a synthetic route to tough mechanical hybrid materials

    International Nuclear Information System (INIS)

    Kusakabe, Akane; Hirota, Ken; Mizutani, Tadashi

    2017-01-01

    Partially phosphorylated poly(vinyl alcohol) was prepared by treating poly(vinyl alcohol) with 100% phosphoric acid, and 5, 10 and 20% of the hydroxyl groups were converted to phosphoric acid ester. Addition of Ca 2+ to an aqueous solution of phosphorylated poly(vinyl alcohol) gave a transparent gel. Five cycles of alternate soaking of the gel in aqueous CaCl 2 and aqueous (NH 4 ) 2 HPO 4 were carried out to crystallise hydroxyapatite (HAP) in the phosphorylated poly(vinyl alcohol) matrix. The X-ray diffraction peaks of HAP formed in 5% phosphorylated PVA were sharp, while those of HAP formed in 20% phosphorylated PVA were broad. The contents of inorganic phase in the hybrid powder were increased from 58 to 76 wt% as the fraction of phosphate groups in the gel was decreased from 20% to 5%. The hybrid powder was first subjected to uniaxial pressing, followed by cold isostatic pressing (CIP) and warm isostatic pressing (WIP) at 120 °C at pressures of 300–980 MPa, to obtain the specimens for three-point bending test. These hybrid specimens showed bending strengths of 15–53 MPa. The hybrid compacts prepared from 10% phosphorylated poly(vinyl alcohol) showed the smallest Young's modulus, the largest displacement at break, and the largest fracture energy, showing that it has the highest toughness among the hybrid materials prepared from poly(vinyl alcohol) with varying degrees of phosphorylation. - Graphical abstract: Densification of hydroxyapatite crystallised in 10% phosphorylated poly(vinyl alcohol) gave the toughest compact. - Highlights: • Hydroxyapatite was crystallised in phosphorylated poly(vinyl alcohol) gels. • Crystallite size of hydroxyapatite decreased as phosphate density was increased. • The hybrid specimens prepared in 10% phosphorylated gel was the toughest. • Phosphate density in organic matrix regulated the mechanical properties of the hybrid.

  20. Preparation of Macroporous Poly (vinyl alcohol-co-triallyl isocyanurate) Beads Bearing Aminocarboxylic Acid as Functional Groups by Suspension Polymerization

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Macroporous poly (vinyl acetate-co-triallyl isocyanurate) beads were prepared with suspension polymerization method. The copolymer beads were then transformed into poly (vinyl alcohol-co-triallyl isocyanurate) by ester exchange reaction. Aminocarboxylic acids were immobilized on the copolymer beads by the esterification of hydroxyl groups with diethyl-lenetriaminepentaacetic bisanhydride. The weak acid exchange capacities, specific surface areas and mean pore diameters of the resultant resin beads were measured.

  1. Chemical modification of poly(vinyl alcohol): evaluation of hydrophilic/lipophilic balance

    International Nuclear Information System (INIS)

    Aranha, Isabele B.; Lucas, Elizabete F.

    2001-01-01

    Poly(vinyl alcohol) terpolymers have been obtained by reaction of partially hydrolized poly(vinyl alcohol) with different acid chlorides. The objective is the preparation of polymers with slight differences in their hydrophilic/lipophilic balance and in the interfacial activities of their solutions. The chemical modifications were characterized by means of 1 H NMR and the polymer properties were evaluated in terms of changes in solubility and surface tension. By chemical modification, polymers with low percentage of hydrophobic group were obtained. The water-soluble polymers obtained did not have the surface tension of their solutions altered. The solubility of the modified polymers decreased markedly, even with low contents of hydrophobic groups. (author)

  2. Study on radiation effect of poly (vinyl alcohol) films irradiated by tritium decay

    International Nuclear Information System (INIS)

    Li Hairong; Peng Shuming; Zhou Xiaosong; Yu Mingming; Xia Lidong; Chen Xiaohua; Liang Jianhua

    2014-01-01

    The radiation effect of poly(vinyl alcohol) films used as a kind of gas-barrier material for inertial confinement fusion (ICF) targets was studied under the different conditions of β-ray from tritium decay. The changes of physical and chemical properties of the irradiated material samples were analyzed by FTIR, XRD and AFM. The tritium-hydrogen isotopic exchange reaction of the irradiated samples mainly occurs at C-H bond and the IR absorption peak of C-T bond obviously increases with the irradiation dose. For strong hydrogen bonding interaction, the isotopic exchange reaction doesn't occur at O-H bond. The crystallinity degree and surface morphology of the irradiated samples were changed. The tensile properties of irradiated poly(vinyl alcohol) films were measured by universal material testing machine. The results show that the change trend of mechanical properties is in accordance with the microstructures of the irradiated samples. (authors)

  3. An Investigation of Chitosan-Grafted-Poly(vinyl alcohol) as an Electrolyte Membrane

    OpenAIRE

    Panu Danwanichakul; Pongchayont Sirikhajornnam

    2013-01-01

    The membrane of chitosan-grafted-poly(vinyl alcohol)/poly(vinyl alcohol) (CS-g-PVA/PVA) was investigated along with chitosan (CS), PVA, CS/PVA, and Nafion 117 membranes for transport properties of water and methanol, mechanical properties, and ionic conductivity. The ionic conductivity, σ, of the crosslinked CS-g-PVA/PVA membrane was about 4.37 mS cm−1 and the methanol permeability, PS, was 1.8×10−7 cm2s−1. These gave the selectivity, σ/PS, of 23.95 mS·s·cm−3 compared with 16.35 mS·s·cm−3 of ...

  4. ANALYSIS OF ADIPATE ESTER CONTENTS IN POLY(VINYL CHLORIDE) PLASTICS

    DEFF Research Database (Denmark)

    Berg, Rolf W.; Otero, Amalia Dopazo

    2006-01-01

    Fourier transform (FT-) Raman spectroscopy excited with a 1064 nm laser can be used to determine the content of plasticizers in commercial flexible poly vinyl chloride (PVC) products. Our previous study [T. Nørbygaard, R.W. Berg, Analysis of phthalate ester content in PVC plastics by means of FT......-Raman Spectroscopy, Appl. Spectrosc. 58 (4) (2004) 410–413]—on detection of the presence of phthalate esters in PVC by FT-Raman spectroscopy — is here extended to the similar case of adipate esters (AEs) in samples of soft poly vinyl chloride plastics. Spectra of a range of adipate ester plasticizers (11 AEs......) in pure form are reported. We studied if qualitative and quantitative determination of the adipate ester content would be possible based on the use of proper reference samples. It was found that AEs as a group cannot be definitively identified by their characteristic Raman bands because other aliphatic...

  5. Thermal and dynamic mechanical properties of grafted kenaf filled poly (vinyl chloride)/ethylene vinyl acetate composites

    International Nuclear Information System (INIS)

    Bakar, Nurfatimah Abu; Chee, Ching Yern; Abdullah, Luqman Chuah; Ratnam, Chantara Thevy; Ibrahim, Nor Azowa

    2015-01-01

    Highlights: • Study on thermal and dynamic mechanical properties of PVC/EVA/PMMA grafted kenaf fiber. • PMMA grafted kenaf fiber showed good interaction with PVC/EVA blends. • Thermal stability of the composites increase upon PMMA grafting on kenaf fiber. • The crystallinity of the composites decrease upon PMMA grafting on kenaf fiber. • PMMA grafted fiber provides more reinforcement on PVC/EVA/grafted PMMA composite. - Abstract: The effects of kenaf and poly (methyl methacrylate grafted kenaf on the thermal and dynamic mechanical properties of poly (vinyl chloride), PVC and ethylene vinyl acetate, EVA blends were investigated. The PVC/EVA/kenaf composites were prepared by mixing the grafted and ungrafted kenaf fiber and PVC/EVA blend using HAAKE Rheomixer at a temperature of 150 °C and the rotor speed at 50 rpm for 20 min. The composites were subjected to Differential Scanning Calorimetric (DSC), Thermogravimetric analysis (TGA), dynamic mechanical analysis (DMA), Fourier transform infrared (FTIR) and Scanning Electron Microscopy (SEM) studies. The DSC data revealed that the crystallinity of the EVA decreased with the addition of 30% grafted and ungrafted kenaf fibers. TGA and derivative thermogravimetric (DTG) curves displayed an increase in the thermal stability of the composites upon grafting of the fiber. Studies on DMA indicate that the T g of the PVC and EVA in the PVC/EVA/kenaf composites has been shifted to higher temperature with the addition of the kenaf fiber. The presence of PMMA on the surface of grafted kenaf fiber was further confirmed by the analytical results from FTIR. The morphology of fractured surfaces of the composites, which was examined by a scanning electron microscope, showed the adhesion between the kenaf fiber and the PVC/EVA matrix was improved upon grafting of the kenaf fiber

  6. Physicochemical characteristics of gamma irradiation crosslinked poly(vinyl alcohol)/magnetite ferrogel composite

    OpenAIRE

    Marinović-Cincović, Milena T.; Radosavljević, Aleksandra N.; Krstić, Jelena I.; Spasojević, Jelena P.; Bibić, Nataša M.; Mitrić, Miodrag N.; Kačarević-Popović, Zorica M.

    2014-01-01

    Magnetic field sensitive gels, ferrogels are new promising class of hydrogels. The coupling of hydrogels and magnetic particles has potential application in soft actuators such as artificial muscles or for hyperthermia application. Here a composite of magnetite particles (Fe3O4) and poly(vinyl alcohol) (PVA) hydrogel is developed using gamma irradiation as a crosslinking agent. PVA and Fe3O4 were chosen because of their well-established biocompatibility, ra...

  7. Fabrication and Characterization of Electrospun Wool Keratin/Poly(vinyl alcohol) Blend Nanofibers

    OpenAIRE

    Shuai Li; Xu-Hong Yang

    2014-01-01

    Wool keratin/poly(vinyl alcohol) (PVA) blend nanofibers were fabricated using the electrospinning method in formic acid solutions with different weight ratios of keratin to PVA. The resultant blend nanofibers were characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR), X-ray diffraction (XRD), thermal gravimetric analysis (TGA), and tensile test. SEM images showed that the diameter of the blend nanofibers was affected by the content of keratin in blend solution...

  8. A poly(vinyl alcohol)/sodium alginate blend monolith with nanoscale porous structure

    OpenAIRE

    Sun, Xiaoxia; Uyama, Hiroshi

    2013-01-01

    A stimuli-responsive poly(vinyl alcohol) (PVA)/sodium alginate (SA) blend monolith with nanoscale porous (mesoporous) structure is successfully fabricated by thermally impacted non-solvent induced phase separation (TINIPS) method. The PVA/SA blend monolith with different SA contents is conveniently fabricated in an aqueous methanol without any templates. The solvent suitable for the fabrication of the present blend monolith by TINIPS is different with that of the PVA monolith. The nanostructu...

  9. Synthesis and characterization of foldable and magnetic field-sensitive, freestanding poly(vinyl acetate)/poly(vinyl chloride)/polyfuran composite and nanocomposite films

    Energy Technology Data Exchange (ETDEWEB)

    Sarıtaş, Sevilay; Eşsiz, Serpil; Sarı, Bekir, E-mail: bsari@gazi.edu.tr

    2017-07-01

    Highlights: • In this study, ternary composite/nanocomposite films were synthesized. • Magnetic field-sensitive folding films were prepared without any elastomer. • Morphological studies show that all composite films have a smooth surface. • The ternary composites/nanocomposite show improved thermal stability compared to the pure PF. - Abstract: In this study, polyfuran and poly(vinyl acetate)/poly(vinyl chloride)/polyfuran ternary composites were synthesized via the chemical polymerization method. The temperature and magnetic field–sensitive novel composites and the nanocomposite were obtained in the form of powders and films. It was observed that the prepared novel conductive films have superior properties at a certain temperature range (25–50 °C) such as bending and folding. The structural properties, thermal behavior, surface morphology, internal structure, and surface roughness of the prepared samples were investigated by various characterization techniques. The conductivities of the samples were measured at room temperature and different temperatures by the four-point technique. X-ray Diffraction analysis results demonstrated that the PF and composites have an amorphous structure, whereas the nanocomposite is in crystalline form. The saturation magnetization (Ms) values of the magnetite and nanocomposite were found to be 58.9 and 5.3 emu g{sup −1}, respectively. It was found that magnetite-doped nanocomposite has superparamagnetic properties at room temperature.

  10. Composite poly(vinyl alcohol/poly(vinyl acetate electrospun nanofibrous mats as a novel wound dressing matrix for controlled release of drugs

    Directory of Open Access Journals (Sweden)

    Jannesari M

    2011-05-01

    Full Text Available Marziyeh Jannesari1, Jaleh Varshosaz2, Mohammad Morshed1, Maedeh Zamani11Department of Textile Engineering, Isfahan University of Technology, Isfahan, Iran; 2Department of Pharmaceutics, School of Pharmacy and Pharmaceutical Sciences Research Center, Isfahan University of Medical Sciences, Isfahan, IranAbstract: The aim of this study was to develop novel biomedicated nanofiber electrospun mats for controlled drug release, especially drug release directly to an injury site to accelerate wound healing. Nanofibers of poly(vinyl alcohol (PVA, poly(vinyl acetate (PVAc, and a 50:50 composite blend, loaded with ciprofloxacin HCl (CipHCl, were successfully prepared by an electrospinning technique for the first time. The morphology and average diameter of the electrospun nanofibers were investigated by scanning electron microscopy. X-ray diffraction studies indicated an amorphous distribution of the drug inside the nanofiber blend. Introducing the drug into polymeric solutions significantly decreased solution viscosities as well as nanofiber diameter. In vitro drug release evaluations showed that both the kind of polymer and the amount of drug loaded greatly affected the degree of swelling, weight loss, and initial burst and rate of drug release. Blending PVA and PVAc exhibited a useful and convenient method for electrospinning in order to control the rate and period of drug release in wound healing applications. Also, the thickness of the blend nanofiber mats strongly influenced the initial release and rate of drug release.Keywords: biodegradable polymers, drug delivery, controlled release, electrospun nanofibers, wound dressing

  11. Incorporation of a Cationic Conjugated Polyelectrolyte CPE within an Aqueous Poly(vinyl alcohol) Sol

    DEFF Research Database (Denmark)

    Knaapila, Matti; Stewart, Beverly; Costa, Telma

    2016-01-01

    We report on a multiscale polymer-within-polymer structure of the cationic conjugated polyelectrolyte poly{[9,9-bis(6-N,N,N-trimethylammonium)hexyl]fluorene phenylene} (HTMAPFP) in aqueous poly(vinyl alcohol).(PVA) sol. Molecular dynamics simulations and small-angle neutron scattering (SANS) data...... show that HTMA-PFP forms aggregates in water but becomes entangled by PVA (with a 1:1 molar ratio of HTMA-PFP to PVA) and eventually immersed in PVA clusters (with the ratio 1:4). This is attributed to the hydrophobic hydrophilic balance. Contrast variation data with regular and deuterated PVA support...

  12. Tailoring the morphology and properties of poly(lactic acid)/poly(ethylene-co-vinyl acetate)/starch blends via reactive compatibilization

    NARCIS (Netherlands)

    Ma, P.; Hristova - Bogaerds, D.G.; Schmit, P.; Goossens, J.G.P.; Lemstra, P.J.

    2012-01-01

    Poly(lactic acid)/poly(ethylene-co-vinyl acetate)/starch (PLA/EVA/starch) ternary blends were prepared by multi-step melt processing (reactive extrusion) in the presence of maleic anhydride (MA), benzoyl peroxide and glycerol. The effects of MA and glycerol concentration on the morphology and

  13. Chemically imaging the effects of the addition of nanofibrillated cellulose on the distribution of poly(acrylic acid) in poly(vinyl alcohol)

    Science.gov (United States)

    Craig Clemons; Julia Sedlmair; Barbara Illman; Rebecca Ibach; Carol Hirschmugl

    2013-01-01

    The distribution of poly(acrylic acid) (PAA) in model laminates of nanocellulose and poly(vinyl alcohol) (PVOH) was investigated by FTIR chemical imaging. The method was effective in spatially discerning the three components of the composite. PAA can potentially improve the performance of nanocellulose reinforced PVOH by not only crosslinking the PVOH matrix but also...

  14. Radiation crosslinking of PVC with polyfunctional monomers

    International Nuclear Information System (INIS)

    Dobo, J.; Takacs, E.; Csato, P.

    1984-01-01

    The radiation crosslinking of PVC in the presence of ethylene glycol dimethacrylate (EGDM) and of trimethylol propane trimethacrylate (TMPTM) was investigated. The effect of PVC powders of different types on the polymerization rate of these monomers was studied by a Calvet-type microcalorimeter. In the milled PVC sheets containing 50 part EGDM a high concentration of trapped free radicals was found by ESR after 16 months storage. (author)

  15. Preparation of poly(vinyl alcohol)/kaolinite nanocomposites via in situ polymerization

    International Nuclear Information System (INIS)

    Jia Xin; Li Yanfeng; Zhang Bo; Cheng Qiong; Zhang Shujiang

    2008-01-01

    Poly(vinyl alcohol)/kaolinite intercalated nanocomposites (Kao-PVA) were prepared via in situ intercalation radical polymerization. Vinyl acetate (VAc) was intercalated into kaolinite by a displacement method using dimethyl sulfoxide/kaolinite (Kao-DMSO) as the intermediate. Then, PVAc/kaolinite (Kao-PVAc) was obtained via radical polymerization with benzoyl peroxide (BPO) as initiator. Last, PVAc/kaolinite was saponified via direct-hydrolysis with NaOH solution in order to obtain PVA/kaolinite nanocomposites, which was characterized by Fourier-Transformation spectroscopy (FTIR), wide X-ray diffraction (WXRD) and transmission electron microscopy (TEM). Their differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) results of the obtained PVA/kaolinite suggested that the thermal properties had an obvious improvement

  16. Evaluation of morphology and cell behaviour of a novel synthesized electrospun poly(vinyl pyrrolidone/poly(vinyl alcohol/hydroxyapatite nanofibers

    Directory of Open Access Journals (Sweden)

    Raheleh Faridi-Majidi

    2017-04-01

    Full Text Available Objective(s: Three-dimensional structures such as nanofibrous scaffolds are being used in biomedical engineering as well as provide a site for cells to attach and proliferate leading to tissue formation. In the present study, poly(vinyl pyrrolidone (PVP/ poly(vinyl alcohol(PVA hybrid nanofibrous scaffold was synthesized by electrospinning. Materials and Methods: The effect of adding nano hydroxyapatite (n-HA and also Epoxypropoxy-propyl-trimethoxysilane (EPPTMS as a crosslinking agent on morphology and cell behaviour of the nanofibers was investigated.Results: Scanning electron microscope (SEM observations showed that all kinds of nanofibers represented uniform and well-ordered morphologies without formation of any beads by controlling the synthesis parameters. The average ûber diameter of PVP-PVA was 260 nm. n-HA was synthesized by wet chemical process. The synthesized n-HA was characterized by XRD for structural analysis. Transmission electron microscope (TEM revealed that HA particles had nanosized dimensions (in the range of 40-100 nm. The presence of n-HA within electrospun PVP-PVA nanofibers was confirmed by XRD and Fourier transmission infrared spectroscopy (FTIR analyses. The average ûber diameter was decreased to 136 nm when n-HA was added in the composition of PVP-PVA. FTIR analysis depicted that PVP-PVA nanofibers were linked to EPPTMS as a biocompatible material by the covalent bond. Although adding n-HA caused to decrease the diameter of PVP-PVA nanofibers, addition of EPPTMS within PVP/PVA/n-HA nanofibers induced increasing distribution of fiber diameter as it enhanced to 195nm. In addition, the proper proliferation of G292 osteoblastic cells without any cytotoxicity was observed for the nanofiber.Conclusion: Since these materials have been known as biomaterials, PVP/PVA/n-HA-EPPTMS nanofibers can be propounded as a good candidate for bone tissue engineering application.

  17. Poly(vinyl alcohol)/poly(acrylic acid)/TiO2/graphene oxide nanocomposite hydrogels for pH-sensitive photocatalytic degradation of organic pollutants

    International Nuclear Information System (INIS)

    Moon, Young-E; Jung, Gowun; Yun, Jumi; Kim, Hyung-Il

    2013-01-01

    Graphical abstract: The photocatalytic removal of pollutants was improved by the two-step mechanism based on the adsorption of pollutants by hydrogel and the effective decomposition by combination of TiO 2 and graphene oxide. -- Highlights: • pH sensitive PVA/PAAc hydrogels were prepared by radical polymerization and condensation reaction. • PVA/PAAc/TiO 2 /graphene oxide nanocomposite hydrogels were used for treatment of basic waste water. • Photocatalytic acitivity of TiO 2 was improved by incorporation of graphene oxide. • Photocatalytic decomposition by nanocomposite hydrogel was improved by increasing pH. -- Abstract: Poly(vinyl alcohol)/poly(acrylic acid)/TiO 2 /graphene oxide nanocomposite hydrogels were prepared using radical polymerization and condensation reaction for the photocatalytic treatment of waste water. Graphene oxide was used as an additive to improve the photocatalytic activity of poly(vinyl alcohol)/poly(acrylic acid)/TiO 2 nanocomposite hydrogels. Both TiO 2 and graphene oxide were immobilized in poly(vinyl alcohol)/poly(acrylic acid) hydrogel matrix for an easier recovery after the waste water treatment. The photocatalytic activity of poly(vinyl alcohol)/poly(acrylic acid)/TiO 2 /graphene oxide nanocomposite hydrogels was evaluated on the base of the degradation of pollutants by using UV spectrometer. The improved removal of pollutants was due to the two-step mechanism based on the adsorption of pollutants by nanocomposite hydrogel and the effective decomposition of pollutants by TiO 2 and graphene oxide. The highest swelling of nanocomposite hydrogel was observed at pH 10 indicating that poly(vinyl alcohol)/poly(acrylic acid)/TiO 2 /graphene oxide nanocomposite hydrogels were suitable as a promising system for the treatment of basic waste water

  18. Effect of graphite loading on the electrical and mechanical properties of Poly (Ethylene Oxide)/Poly (Vinyl Chloride) polymer films

    Science.gov (United States)

    Hajar, M. D. S.; Supri, A. G.; Hanif, M. P. M.; Yazid, M. I. M.

    2017-10-01

    In this study, films consisting of a blend of poly (ethylene oxide)/poly (vinyl chloride) (PEO/PVC) and a conductive filler, graphite were prepared and characterized for their mechanical and electrical properties. Solid polymer blend films based on PEO/PVC (50/50 wt%/wt%) with different graphite loading were prepared by using solution casting technique. Electrical conductivity results discovered the conductivity increased with increasing of filler loading. However, increasing amount of graphite loading led to a decreased in tensile strength and young’s modulus of PEO/PVC/Graphite polymer films. The dispersion of graphite and mechanism of conductive path in the polymer films were also investigated by scanning electron microscopy (SEM). The morphology of the PEO/PVC/Graphite polymer films shows that agglomeration occurred to complete the connection of conductive path, thus improving the conductivity behavior of the polymer films.

  19. Sorption of Different Dye Wastes By Poly(vinyl alcohol) /Poly (Carboxymethyl Cellulose) Blend Grafted Through A Radiation Method

    International Nuclear Information System (INIS)

    El-Salmawi Kariman, M.; Abu Zaid Magda, M.; Ibraheim Sayeda, M.; El-Naggar Abdel Wahab, M.; Zahran Abdel Hamid, H.

    1999-01-01

    The sorption of different dye wastes normaly released from industrial textile factories by a graft copolymer of poly(vinyl alcohol)/poly(carboxymethyl cellulose) blend with polystyrene has been investigated. The dye sorption was evaluated at different conditions. The amount of sorbed dye was determined by using a spectroscopic method. The blend graft copolymer showed a relatively high sorption for basic dye than other dyestuffs such as acid, reactive and direct. Moreover, it was found that the dye sorption did not depend on the weight of the blend graft copolymer or the volume of the waste solution. The treatment of the dye waste by using the prepared blend graft copolymer may be considered a practical one from the point of view of environmental methods

  20. Preparation of Citric Acid Crosslinked Chitosan/Poly(Vinyl Alcohol Blend Membranes for Creatinine Transport

    Directory of Open Access Journals (Sweden)

    Retno Ariadi Lusiana

    2016-08-01

    Full Text Available Preparation of membrane using crosslinking reaction between chitosan and citric acid showed that functional group modification increased the number of active carrier groups which lead to better transport capacity of the membrane. In addition, the substitution of the carboxyl group increased creatinine permeation of chitosan membrane. The transport capacity of citric acid crosslinked chitosan membrane for creatinine was found to be 6.3 mg/L. The presence of cyanocobalamin slightly hindered the transport of creatinine although compounds did not able to pass through citric acid crosslinked chitosan/poly(vinyl alcohol blend membrane, as compounds no found in the acceptor phase.

  1. Crossover from Rouse dynamics to the α- relaxation in a poly(vinyl ethylene)

    International Nuclear Information System (INIS)

    Arbe, A.; Colmenero, J.; Richter, D.; Monkenbusch, M.; Willner, L.; Farago, B.

    2004-01-01

    By means of neutron spin echo (NSE) we have explored the dynamics of poly(vinyl ethylene) on length scales covering Rouse dynamics and below. The results establish the simultaneous existence of a generic sublinear diffusion regime which underlies the α-process in addition to the Rouse process. Both regimes are separated by a well- defined dynamic crossover. From that the size of the Gaussian blobs making up the Rouse model is determined directly. The glassy dynamics may thus be identified with subdiffusive motions occurring within these Gaussian blobs. (author)

  2. Study on properties of poly(vinyl alcohol/polyacrylonitrile blend film

    Directory of Open Access Journals (Sweden)

    Guoquan Zhu

    2013-01-01

    Full Text Available In this work, a series of poly(vinyl alcohol (PVA/polyacrylonitrile (PAN blend films with different PAN mole contents were prepared by casting the polymer blend solution in dimethylsulfoxide (DMSO. Surface morphologies of PVA/PAN blend films were analyzed by Scanning Electronic Microscopy (SEM and Atomic Force Microscopy (AFM. Thermal, mechanical, and chemical properties of PVA/PAN blend films were investigated by Differential Scanning Calorimetry (DSC, Thermogravimetric Analysis (TGA, Tensile Tests, and Surface Contact Angle Tests. The results showed that the introduction of PAN could exert marked effects on the properties of PVA films.

  3. Biodegradability of poly(3-hydroxybutyrate) film grafted with vinyl acetate: Effect of grafting and saponification

    Science.gov (United States)

    Wada, Yuki; Seko, Noriaki; Nagasawa, Naotsugu; Tamada, Masao; Kasuya, Ken-ichi; Mitomo, Hiroshi

    2007-06-01

    Radiation-induced graft polymerization of vinyl acetate (VAc) onto poly(3-hydroxybutyrate) (PHB) film was carried out. At a degree of grafting higher than 5%, the grafted films (PHB-g-VAc) completely lost the enzymatic degradability that is characteristic of PHB due to the grafted VAc covering the surface of the PHB film. However, the biodegradability of the PHB-g-VAc films was recovered when the films were saponified in alkali solution under optimum conditions. Graft chains of the PHB-g-VAc film reacted selectively to become biodegradable polyvinyl alcohol (PVA). The biodegradability of the saponified PHB-g-VAc film increased rapidly with time.

  4. Study on dehydrochlorination of waste poly (vinyl chloride) resins by microwave irradiation

    Science.gov (United States)

    Moriwaki, Saburo; Qian, Qingrong; Sunohara, Satoshi; Machida, Motoi; Tatsumoto, Hideki

    Waste poly (vinyl chloride: PVC) resins are experimentally dehydrochlorinated by microwave irradiation. The following unique results are obtained: (1) plasticizer in PVC resin absorbs microwave power more effectively than PVC polymer. The higher the plasticizer content in PVC resin, the higher is the dehydrochlorination reaction (2) low PVC polymer content materials such as cushion floor require high microwave irradiation power to secure a high dehydrochlorination yield, (3) calcium carbonate in PVC resin reacts with released hydrochloric acid gas and results calcium chloride during microwave irradiation, (4) additives in PVC resin strongly influence dehydrochlorination yield, (5) it is evidenced that the PVC copolymer is also dehydrochlorinated by microwave irradiation.

  5. Effect of borax concentration on the structure of Poly(Vinyl Alcohol) gels

    Science.gov (United States)

    Lawrence, Mathias B.; Desa, J. A. E.; Aswal, V. K.

    2012-06-01

    Poly(Vinyl Alcohol) hydrogels cross-linked with varying concentrations of borax have been studied using Small-Angle Neutron Scattering and X-Ray Diffraction. The intensity of scattering increases with borax concentration from 1 mg/ml up to 2 mg/ml and falls thereafter for 4 mg/ml, increasing again for a concentration of 10 mg/ml. The mesoscopic structural changes that cause these trends in the SANS data are in keeping with the variations in the X-ray diffraction patterns pertaining to structures within the PVA chains.

  6. Biodegradability of poly(3-hydroxybutyrate) film grafted with vinyl acetate: Effect of grafting and saponification

    International Nuclear Information System (INIS)

    Wada, Yuki; Seko, Noriaki; Nagasawa, Naotsugu; Tamada, Masao; Kasuya, Ken-ichi; Mitomo, Hiroshi

    2007-01-01

    Radiation-induced graft polymerization of vinyl acetate (VAc) onto poly(3-hydroxybutyrate) (PHB) film was carried out. At a degree of grafting higher than 5%, the grafted films (PHB-g-VAc) completely lost the enzymatic degradability that is characteristic of PHB due to the grafted VAc covering the surface of the PHB film. However, the biodegradability of the PHB-g-VAc films was recovered when the films were saponified in alkali solution under optimum conditions. Graft chains of the PHB-g-VAc film reacted selectively to become biodegradable polyvinyl alcohol (PVA). The biodegradability of the saponified PHB-g-VAc film increased rapidly with time

  7. Poly(vinyl acetate)/clay nanocomposite materials for organic thin film transistor application.

    Science.gov (United States)

    Park, B J; Sung, J H; Park, J H; Choi, J S; Choi, H J

    2008-05-01

    Nanocomposite materials of poly(vinyl acetate) (PVAc) and organoclay were fabricated, in order to be utilized as dielectric materials of the organic thin film transistor (OTFT). Spin coating condition of the nanocomposite solution was examined considering shear viscosity of the composite materials dissolved in chloroform. Intercalated structure of the PVAc/clay nanocomposites was characterized using both wide-angle X-ray diffraction and TEM. Fracture morphology of the composite film on silicon wafer was also observed by SEM. Dielectric constant (4.15) of the nanocomposite materials shows that the PVAc/clay nanocomposites are applicable for the gate dielectric materials.

  8. Graft Copolymerization of Styrene from Poly(vinyl alcohol via RAFT Process

    Directory of Open Access Journals (Sweden)

    Gholam Ali Koohmareh

    2011-01-01

    Full Text Available Polystyrene, PS, was grafted from poly(vinyl alcohol, PVA, backbone by reversible addition-fragmentation chain transfer (RAFT polymerization. The hydroxyl groups of the PVA were converted into aromatic dithioester RAFT agent and polymerization began in the presence of this agent. The structure of compounds was confirmed by FT-IR and 1HNMR spectroscopy. The graft copolymer was characterized by thermogravimetric analysis (TGA, X-ray diffraction (XRD, and scanning electron microscopy (SEM. Grafted polystyrene chains were cleaved from the PVA backbone by acidic hydrolysis of the PVA-g-PS, and its polydispersity index, PDI, was determined by gel permeation chromatography (GPC showing narrow molecular weight distribution.

  9. Characterization of nanocellulose reinforced semi-interpenetrating polymer network of poly(vinyl alcohol) & polyacrylamide composite films.

    Science.gov (United States)

    Mandal, Arup; Chakrabarty, Debabrata

    2015-12-10

    Semi-interpenetrating polymer network (semi-IPN) of poly(vinyl alcohol)/polyacrylamide was reinforced with various doses of nanocellulose. The different composite films thus prepared were characterized with respect to their mechanical, thermal, morphological and barrier properties. The composite film containing 5 wt.% of nanocellulose showed the highest tensile strength. The semi-interpenetrating polymer network of poly(vinyl alcohol)/polyacrylamide; and its various composites with nanocellulose were almost identical in their thermal stability. Each of the composites however exhibited much superior stability with respect to the linear poly(vinyl alcohol) and crosslinked polyacrylamide. The scanning electron microscopy (SEM) and atomic force microscopy (AFM) studies exhibited phase separated morphology where agglomerates of nanocellulose were found to be dispersed in the matrix of the semi-IPN. The moisture vapor transmission rate (MVTR) was the lowest for the film containing 5 wt.% of nanocellulose. Copyright © 2015 Elsevier Ltd. All rights reserved.

  10. Poly(vinyl pyrrolidone) (PVP) hydrogels study for ophthalmologic area utilization

    International Nuclear Information System (INIS)

    Amaral, Renata Hage; Rogero, Sizue Ota; Lugao, Ademar Benevolo; Cruz, Aurea S.; Sacramento, Rogerio S.; Lima Filho, Acacio A. Souza; Schor, Paulo

    2005-01-01

    Poly (vinyl pyrrolidone) (PVP) hydrogels produced by radiation-induced crosslinking were studied to compose drug delivery system to be used in the eye surface and to manufacture ophthalmic plugs. Some formulations with PVP and poly ethylene glycol (PEG) with different molar mass (300 and 600) were prepared utilizing 0.85% sodium chloride aimed to control the swelling capacity. The obtained hydrogels were characterized by gel fraction and swelling assays. The gel fraction and swelling results indicated no difference in the formulation containing or not NaCl. The gel fraction results varied from 62 to 81% and the swelling degree from 130 to 420%. In vitro assay of cytotoxicity by neutral red uptake method was the first biocompatibility test performed. The results showed no evidence of toxicity in the studied hydrogels. (author)

  11. Poly(vinyl alcohol) cryogel phantoms for use in ultrasound and MR imaging

    International Nuclear Information System (INIS)

    Surry, K J M; Austin, H J B; Fenster, A; Peters, T M

    2004-01-01

    Poly(vinyl alcohol) cryogel, PVA-C, is presented as a tissue-mimicking material, suitable for application in magnetic resonance (MR) imaging and ultrasound imaging. A 10% by weight poly(vinyl alcohol) in water solution was used to form PVA-C, which is solidified through a freeze-thaw process. The number of freeze-thaw cycles affects the properties of the material. The ultrasound and MR imaging characteristics were investigated using cylindrical samples of PVA-C. The speed of sound was found to range from 1520 to 1540 m s -1 , and the attenuation coefficients were in the range of 0.075-0.28 dB (cm MHz) -1 . T1 and T2 relaxation values were found to be 718-1034 ms and 108-175 ms, respectively. We also present applications of this material in an anthropomorphic brain phantom, a multi-volume stenosed vessel phantom and breast biopsy phantoms. Some suggestions are made for how best to handle this material in the phantom design and development process

  12. Novel proton exchange membrane based on crosslinked poly(vinyl alcohol) for direct methanol fuel cells

    Science.gov (United States)

    Liu, Chien-Pan; Dai, Chi-An; Chao, Chi-Yang; Chang, Shoou-Jinn

    2014-03-01

    In this study, we report the synthesis and the characterization of poly (vinyl alcohol) based proton conducting membranes. In particular, we describe a novel physically and chemically PVA/HFA (poly (vinyl alcohol)/hexafluoroglutaric acid) blending membranes with BASANa (Benzenesulfonic acid sodium salt) and GA (Glutaraldehyde) as binary reaction agents. The key PEM parameters such as ion exchange capacity (IEC), water uptake, proton conductivity, and methanol permeability were controlled by adjusting the chemical composition of the membranes. The IEC value of the membrane is found to be an important parameter in affecting water uptake, conductivity as well as the permeability of the resulting membrane. Plots of the water uptake, conductivity, and methanol permeability vs. IEC of the membranes show a distinct change in the slope of their curves at roughly the same IEC value which suggests a transition of structural changes in the network. The proton conductivities and the methanol permeability of all the membranes are in the range of 10-3-10-2 S cm-1 and 10-8-10-7 cm2 s-1, respectively, depending on its binary crosslinking density, and it shows great selectivity compared with those of Nafion®-117. The membranes display good mechanical properties which suggest a good lifetime usage of the membranes applied in DMFCs.

  13. An Investigation of Chitosan-Grafted-Poly(vinyl alcohol as an Electrolyte Membrane

    Directory of Open Access Journals (Sweden)

    Panu Danwanichakul

    2013-01-01

    Full Text Available The membrane of chitosan-grafted-poly(vinyl alcohol/poly(vinyl alcohol (CS-g-PVA/PVA was investigated along with chitosan (CS, PVA, CS/PVA, and Nafion 117 membranes for transport properties of water and methanol, mechanical properties, and ionic conductivity. The ionic conductivity, σ, of the crosslinked CS-g-PVA/PVA membrane was about 4.37 mS cm−1 and the methanol permeability, PS, was 1.8×10−7 cm2s−1. These gave the selectivity, σ/PS, of 23.95 mS·s·cm−3 compared with 16.35 mS·s·cm−3 of Nafion 117 membrane. The conductivity of the crosslinked CS-g-PVA/PVA membrane was greater than others including Nafion 117 when the membranes were saturated with methanol solution of which concentration was greater than 20%. This fact and that the mechanical properties of the wet crosslinked CS-g-PVA/PVA membrane were comparable to those of other membranes made it a promising material to be used as an electrolyte membrane in a direct methanol fuel cell.

  14. DIELECTRIC AND PYROELECTRIC PROPERTIES OF THE COMPOSITES OF FERROELECTRIC CERAMIC AND POLY(VINYL CHLORIDE

    Directory of Open Access Journals (Sweden)

    M.Olszowy

    2003-01-01

    Full Text Available The dielectric and pyroelectric properties of lead zirconate titanate/poly(vinyl chloride [PZT/PVC] and barium titanate/poly(vinyl chloride [BaTiO3/ PVC] composites were studied. Flexible composites were fabricated in the thin films form (200-400 μm by hot-pressed method. Powders of PZT or BaTiO3 in the shape of ≤ 75 μm ceramics particles were dispersed in a PVC matrix, providing composites with 0-3} connectivity. Distribution of the ceramic particles in the polymer phase was examined by scanning electron microscopy. The analysis of the thermally stimulated currents (TSC have also been done. The changes of dielectric and pyroelectric data on composites with different contents of ceramics up to 40% volume were investigated. The dielectric constants were measured in the frequency range from 600 Hz to 6 MHz at room temperature. The pyroelectric coefficient for BaTiO3/PVC composite at 343 K is about 35 μC/m2K which is higher than that of β-PVDF (10 μC/m2 K.

  15. Cosolvent gel-like materials from partially hydrolyzed poly(vinyl acetate)s and borax.

    Science.gov (United States)

    Angelova, Lora V; Terech, Pierre; Natali, Irene; Dei, Luigi; Carretti, Emiliano; Weiss, Richard G

    2011-09-20

    A gel-like, high-viscosity polymeric dispersion (HVPD) based on cross-linked borate, partially hydrolyzed poly(vinyl acetate) (xPVAc, where x is the percent hydrolysis) is described. Unlike hydro-HVPDs prepared from poly(vinyl alcohol) (PVA) and borate, the liquid portion of these materials can be composed of up to 75% of an organic cosolvent because of the influence of residual acetate groups on the polymer backbone. The effects of the degree of hydrolysis, molecular weight, polymer and cross-linker concentrations, and type and amount of organic cosolvent on the rheological and structural properties of the materials are investigated. The stability of the systems is explored through rheological and melting-range studies. (11)B NMR and small-angle neutron scattering (SANS) are used to probe the structure of the dispersions. The addition of an organic liquid to the xPVAc-borate HVPDs results in a drastic increase in the number of cross-linked borate species as well as the agglomeration of the polymer into bundles. These effects result in an increase in the relaxation time and thermal stability of the networks. The ability to make xPVAc-borate HVPDs with very large amounts of and rather different organic liquids, with very different rheological properties that can be controlled easily, opens new possibilities for applications of PVAc-based dispersions. © 2011 American Chemical Society

  16. Facile preparation of layered double hydroxide/MoS{sub 2}/poly(vinyl alcohol) composites

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Keqing, E-mail: zhoukq@cug.edu.cn [Faculty of Engineering, China University of Geosciences (Wuhan), 388 Lumo Road, Wuhan, Hubei, 430074 (China); Hu, Yixin [Department of Chemistry, Lanzhou University, Lanzhou 730000 (China); Liu, Jiajia [State Key Laboratory of Fire Science, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui, 230026 (China); Gui, Zhou, E-mail: zgui@ustc.edu.cn [State Key Laboratory of Fire Science, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui, 230026 (China); Jiang, Saihua [School of Mechanical and Automotive Engineering, South China University of Technology, Wushan Road 381, Guangzhou, 510641 (China); Tang, Gang [School of Architecture and Civil Engineering, Anhui University of Technology, 59 Hudong Road, Ma' anshan, Anhui, 243002 (China)

    2016-08-01

    In present study, the layered double hydroxide/MoS{sub 2} hybrids are facilely synthesized by self-assembly of exfoliated MoS{sub 2} nanosheets and layered double hydroxide nanoplates via electrostatic interaction, with the aim of combining their physical and chemical functionalities to form a promising nanofiller for flame retardancy in polymer composites. The structure and morphology of the layered double hydroxide/MoS{sub 2} hybrids are probed by X-ray diffraction and transmission electron microscopy. Subsequently, the hybrids are incorporated into poly (vinyl alcohol) to serve as reinforcements. The flame retardant efficiency of MoS{sub 2} nanosheets in poly (vinyl alcohol) is significantly enhanced after the incorporation of layered double hydroxide nanoplates, which can be explained by the forming of a compact and uniform char during combustion. - Highlights: • The LDH/MoS{sub 2} hybrids were facilely synthesized by self-assembly method. • The flame retardant efficiency of LDH/MoS{sub 2} hybrids in PVA was significantly enhanced. • It is a promising strategy for improving the flame retardant efficiency of MoS{sub 2}.

  17. Preparation and characterization of reactive blends of poly(lactic acid), poly(ethylene-co-vinyl alcohol), and poly(ethylene-co-glycidyl methacrylate)

    International Nuclear Information System (INIS)

    Warangkhana, Phromma; Rathanawan, Magaraphan; Jana Sadhan, C.

    2015-01-01

    The ternary blends of poly(lactic acid) (PLA), poly(ethylene-co-vinyl alcohol) (EVOH), and poly(ethylene-co-glycidyl methacrylate) (EGMA) were prepared. The role of EGMA as a compatibilizer was evaluated. The weight ratio of PLA:EVOH was 80:20 and the EGMA loadings were varied from 5-20 phr. The blends were characterized as follows: thermal properties by differential scanning calorimetry, morphology by scanning electron microscopy, and mechanical properties by pendulum impact tester, and universal testing machine. The glass transition temperature of PLA blends did not change much when compared with that of PLA. The blends of PLA/EGMA and EVOH/EGMA showed EGMA dispersed droplets where the latter led to poor impact properties. However, the tensile elongation at break and tensile toughness substantially increased upon addition of EGMA to blends of PLA and EVOH. It was noted in tensile test samples that both PLA and EVOH domains fibrillated significantly to produce toughness

  18. Preparation and characterization of reactive blends of poly(lactic acid), poly(ethylene-co-vinyl alcohol), and poly(ethylene-co-glycidyl methacrylate)

    Energy Technology Data Exchange (ETDEWEB)

    Warangkhana, Phromma; Rathanawan, Magaraphan, E-mail: rathanawan.k@chula.ac.th [Chulalongkorn University, Petroleum and Petrochemical College - Bangkok (Thailand); Jana Sadhan, C., E-mail: janas@uakron.edu [The University of Akron, Department of Polymer Engineering, Ohio (United States)

    2015-05-22

    The ternary blends of poly(lactic acid) (PLA), poly(ethylene-co-vinyl alcohol) (EVOH), and poly(ethylene-co-glycidyl methacrylate) (EGMA) were prepared. The role of EGMA as a compatibilizer was evaluated. The weight ratio of PLA:EVOH was 80:20 and the EGMA loadings were varied from 5-20 phr. The blends were characterized as follows: thermal properties by differential scanning calorimetry, morphology by scanning electron microscopy, and mechanical properties by pendulum impact tester, and universal testing machine. The glass transition temperature of PLA blends did not change much when compared with that of PLA. The blends of PLA/EGMA and EVOH/EGMA showed EGMA dispersed droplets where the latter led to poor impact properties. However, the tensile elongation at break and tensile toughness substantially increased upon addition of EGMA to blends of PLA and EVOH. It was noted in tensile test samples that both PLA and EVOH domains fibrillated significantly to produce toughness.

  19. Effect of homopolymer poly(vinyl acetate on compatibility and mechanical properties of poly(propylene carbonate/poly(lactic acid blends

    Directory of Open Access Journals (Sweden)

    J. Gao

    2012-11-01

    Full Text Available A small amount of homopolymer poly(vinyl acetate (PVAc is used to compatibilize the biodegradable blends of poly(propylene carbonate (PPC and poly(lactic acid (PLA. Scanning electron microscopy (SEM and differential scanning calorimetry (DSC results show that PVAc is selectively localized in the PLA phase and at the interface between PPC and PLA phases. As a result, these interface-localized PVAc layers act as not only a compatibilizer to improve the phase dispersion significantly but also a bridge to increase the interfacial adhesion between PPC and PLA phases dramatically. Both of them are believed to be responsible for the enhancement in mechanical properties. This work provides a simple avenue to fabricate eco-friendly PPC/PLA blends with high performance, and in some cases, reducing the demand for petroleumbased plastics such as polypropylene.

  20. Investigation of Complexation of Linear Poly(N-vinyl-2-pyrrolidone with Poly(methacrylic acid-co-methyl methacrylate Gel

    Directory of Open Access Journals (Sweden)

    Guoqin Liu

    2011-01-01

    Full Text Available The contraction of poly(methacrylic acid-co-methyl methacrylate (P(MAA-co-MMA gel induced by complexation with linear poly(N-vinyl-2-pyrrolidone (PVP is quite different from that of poly(acrylic acid (PAA or poly(methacrylic acid (PMAA gel. It was found that the concentration of PVP has a strong effect on the complexation with P(MAA-co-MMA gel. When PVP was introduced into the P(MAA-co-MMA network, its dynamic mechanic properties vary greatly between complexed and uncomplexed networks. It had the following results: (1 the higher modulus ratio; (2 a slight contraction of gel.

  1. Investigation of Complexation of Linear Poly(N-vinyl-2-pyrrolidone) with Poly(methacrylic acid-co-methyl methacrylate) Gel

    OpenAIRE

    Liu, Guoqin; Yan, Guojin; Zou, Wenjun; Li, Zhengxin

    2011-01-01

    The contraction of poly(methacrylic acid-co-methyl methacrylate) (P(MAA-co-MMA)) gel induced by complexation with linear poly(N-vinyl-2-pyrrolidone) (PVP) is quite different from that of poly(acrylic acid) (PAA) or poly(methacrylic acid) (PMAA) gel. It was found that the concentration of PVP has a strong effect on the complexation with P(MAA-co-MMA) gel. When PVP was introduced into the P(MAA-co-MMA) network, its dynamic mechanic properties vary greatly between complexed and uncomplexed netwo...

  2. Preparation of poly(vinyl alcohol)-grafted graphene oxide/poly(vinyl alcohol) nanocomposites via in-situ low-temperature emulsion polymerization and their thermal and mechanical characterization

    Science.gov (United States)

    Zhang, Shengchang; Liu, Pengqing; Zhao, Xiangsen; Xu, Jianjun

    2017-02-01

    An in-situ polymerization combined with chemical grafting modification method for preparing Poly(vinyl alcohol)-grafted graphene oxide/Poly(vinyl alcohol) (PVA-g-GO/PVA) nanocomposites was reported. Firstly, Poly(vinyl acetate)-grafted graphene oxide/Poly(vinyl acetate) nanocomposites were prepared, and then the PVA-g-GO/PVA nanocomposites could be obtained through alcoholysis reaction. X-ray photoelectron spectrometer and fourier-transform infrared spectrometer confirmed that the PVAc or PVA chains were successfully grafted to GO sheets during in-situ polymerization and alcoholysis. And the results from transmission electron microscopy, scanning electron microscopy and X-ray diffraction showed that the well compatibility and homogenous dispersion of PVA-g-GO in PVA matrix could be achieved. Differential scanning calorimetric, thermogravimetry analysis and tensile test were employed to study the thermal and mechanical properties of the PVA-g-GO/PVA nanocomposites. The results indicated that a 53% improvement of tensile strength and a 36% improvement of Young's modulus were achieved by addition of 0.5 wt% of GO sheets. And the glass transition temperature of PVA-g-GO/PVA nanocomposites was increased, and their thermal stability and crystallization degree were both decreased. Due to well dispersion of fillers and strong interfacial interactions at the filler-matrix interface, in-situ polymerization combined with chemical grafting modification was a good choice to prepare graphene/PVA nanocomposite with excellent mechanical properties.

  3. Thermodynamic and Kinetic Behavior of the Polystyrene/Poly(vinyl methyl ether) Blend as Studied by Excimer Fluorescence.

    Science.gov (United States)

    1986-01-02

    AD-A±63 895 THERMODYNAMIC AND KINETIC BEHAVIOR OF THE / POLYSTYRENE/POLY(YINYL METHYL E..(U) STANFORD UNIY CALIFDEPT OF CHEMICAL ENGINEERING C N...Polystyrene/Poly(vinyl methyl ether) Blend 7. DEcFRMN 81 toOR 30USptE8 00~ as Studied by Excimer Fluorescence 6 EFRIGOG EOTNME *AUTHOR() a. CONTRACT OR GRANT...werea fondoare ihemoriisof * ~ Ex e sp fluodecositionsdu to deud Gen e and hoog Pinus Florsneis shownhase migrationprocSECURITY CLASIFICTIO OFd

  4. Highly sensitive and ultrafast response surface acoustic wave humidity sensor based on electrospun polyaniline/poly(vinyl butyral) nanofibers

    International Nuclear Information System (INIS)

    Lin Qianqian; Li Yang; Yang Mujie

    2012-01-01

    Highlights: ► Polyanline/poly(vinyl butyral) nanofibers are prepared by electrospinning. ► Nanofiber-based SAW humidity sensor show high sensitivity and ultrafast response. ► The SAW sensor can detect very low humidity. - Abstract: Polyaniline (PANi) composite nanofibers were deposited on surface acoustic wave (SAW) resonator with a central frequency of 433 MHz to construct humidity sensors. Electrospun nanofibers of poly(methyl methacrylate), poly(vinyl pyrrolidone), poly(ethylene oxide), poly(vinylidene fluoride), poly(vinyl butyral) (PVB) were characterized by scanning electron microscopy, and humidity response of corresponding SAW humidity sensors were investigated. The results indicated that PVB was suitable as a matrix to form nanofibers with PANi by electrospinning (ES). Electrospun PANi/PVB nanofibers exhibited a core–sheath structure as revealed by transmittance electron microscopy. Effects of ES collection time on humidity response of SAW sensor based on PANi/PVB nanofibers were examined at room temperature. The composite nanofiber sensor exhibited very high sensitivity of ∼75 kHz/%RH from 20 to 90%RH, ultrafast response (1 s and 2 s for humidification and desiccation, respectively) and good sensing linearity. Furthermore, the sensor could detect humidity as low as 0.5%RH, suggesting its potentials for low humidity detection. Attempts were done to explain the attractive humidity sensing performance of the sensor by considering conductivity, hydrophilicity, viscoelasticity and morphology of the polymer composite nanofibers.

  5. Miscibility and specific interactions in blends of poly(n-vinyl-2-pyrrolidone) and acid functional polyester resins.

    NARCIS (Netherlands)

    Senatore, D.; Berix, M.J.A.; Laven, J.; Benthem, van R.A.T.M.; With, de G.; Mezari, B.; Magusin, P.C.M.M.

    2008-01-01

    Miscibility and intermol. interactions of novel blends of poly(N-vinyl-2-pyrrolidone) (PVP) and acid functional polyester resins (APE) were studied by use of Differential Scanning Calorimetry (DSC), Attenuated Total Reflectance Fourier Transform IR (ATR-FTIR), Cross-Polarization Magic Angle Spinning

  6. Poly(vinyl alcohol)/cellulose nanofibril hybrid aerogels with an aligned microtubular porous structure and their composites with polydimethylsiloxane

    Science.gov (United States)

    Tianliang Zhai; Qifeng Zheng; Zhiyong Cai; Lih-Sheng Turng; Hesheng Xia; Shaoqin Gong

    2015-01-01

    Superhydrophobic poly(vinyl alcohol) (PVA)/ cellulose nanofibril (CNF) aerogels with a unidirectionally aligned microtubular porous structure were prepared using a unidirectional freeze-drying process, followed by the thermal chemical vapor deposition of methyltrichlorosilane. The silanized aerogels were characterized using various techniques including scanning...

  7. Synthesis of iron nanoparticles with poly(1-vinylpyrrolidone-co-vinyl acetate) and its application to nitrate reduction

    DEFF Research Database (Denmark)

    Lee, Nara; Choi, Kyunghoon; Uthuppu, Basil

    2014-01-01

    This study aimed to synthesize dispersed and reactive nanoscale zero-valent iron (nZVI) with poly(1-vinylpyrrolidone-co-vinyl acetate) (PVP/VA), nontoxic and biodegradable stabilizer. The nZVI used for the experiments was prepared by reduction of ferric solution in the presence of PVP/VA with spe...

  8. IR Laser-Induced Degradation of Poly(vinyl acetate): Novel Thermal Reactions in the Solid Polymers

    Czech Academy of Sciences Publication Activity Database

    Kupčík, Jaroslav; Blazevska-Gilev, J.; Pola, Josef

    2005-01-01

    Roč. 26, č. 5 (2005), s. 386-389 ISSN 1022-1336 R&D Projects: GA ČR(CZ) GA104/04/2028 Institutional research plan: CEZ:AV0Z40720504 Keywords : laser ablation * laser-induced polymers * poly(vinyl acetate) Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.126, year: 2005

  9. In vitro and in vivo study to the biocompatibility and biodegradation of hydroxyapatite/poly(vinyl alcohol)/gelatin composite.

    NARCIS (Netherlands)

    Wang, M.; Li, Y.; Wu, J.; Xu, F.; Zuo, Y.; Jansen, J.A.

    2008-01-01

    A novel porous composite material composed of hydroxyapatite, poly(vinyl alcohol) (PVA), and gelatin (Gel) was fabricated by emulsification. Scanning electron microscopy showed that the material had a well-interconnected porous structure including many macropores (100-500 microm) and micropores

  10. The influence of Poly-Vinyl-Chloride tubing on the isolated perfused rat´s heart.

    NARCIS (Netherlands)

    Meijler, F.L.; Durrer, D.

    1950-01-01

    There are types of poly-vinyl-chloride tubing sold and used for medical and biological purposes which deteriorate heart action in a few minutes. A simple method for testing P.V.C. tubing can be found in the isolated rat's he art perfused according to Langendorff.

  11. Morphology in binary blends of poly(vinyl methyl ether) and epsilon-caprolactone-trimethylene carbonate diblock copolymer

    NARCIS (Netherlands)

    Luyten, MC; Bogels, EJF; vanEkenstein, GORA; tenBrinke, G; Bras, W; Komanschek, BE; Ryan, AJ

    The morphology of symmetric diblock copolymer of epsilon-caprolactone (PCL) and trimethylene carbonate (PTMC), in blends with poly(vinyl methyl ether) (PVME) is investigated with (modulated) differential scanning calorimetry (d.s.c.), time resolved small angle (SAXS) and wide angle (WAXS) X-ray

  12. Morphology in binary blends of poly(vinyl methyl ether) and ε-caprolactone-trimethylene carbonate diblock copolymer

    NARCIS (Netherlands)

    Luyten, M.C.; Bögels, E.J.F.; Alberda van Ekenstein, G.O.R.; Brinke, G. ten; Bras, W.; Komanschek, B.E.; Ryan, A.J.

    1997-01-01

    The morphology of symmetric diblock copolymer of ε-caprolactone (PCL) and trimethylene carbonate (PTMC), in blends with poly(vinyl methyl ether) (PVME) is investigated with (modulated) differential scanning calorimetry (d.s.c.), time resolved small angle (SAXS) and wide angle (WAXS) X-ray

  13. Poly(vinyl alcohol) composite films with high percent elongation prepared from amylose-fatty ammonium salt inclusion complexes

    Science.gov (United States)

    Amylose inclusion complexes prepared from cationic fatty ammonium salts and jet-cooked high amylose starch were combined with poly(vinyl alcohol) (PVOH) to form glycerol-plasticized films. Their tensile properties were compared with similar films prepared previously with analogous anionic fatty acid...

  14. Analysis of phthalate ester content in poly(vinyl chloride) plastics by means of Fourier transform Raman spectroscopy

    DEFF Research Database (Denmark)

    Nørbygaard, Thomas; Berg, Rolf W.

    2004-01-01

    Fourier transform (FT) Raman spectroscopy is applied to a range of phthalate ester plasticizers in pure form as well as in poly(vinyl chloride) (PVC) samples. It is found that phthalate esters as a group can be identified by a set of six characteristic Raman bands. FT-Raman spectra of 22 phthalate...

  15. Improving the Performances of Poly(vinylphosphonic acid) by Compositing or Copolymerization with Poly(4-(α-methyl)vinyl-1H-1,2,3-triazole)

    International Nuclear Information System (INIS)

    Han, Shuaiyuan; Yue, Baohua; Yan, Liuming

    2014-01-01

    Graphical abstract: - Highlights: • Poly(4-(α-methyl)vinyl-1H-1,2,3-triazole) is synthesized • PVPA/PMVTri polymeric composite proton conducting membranes are prepared • The proton conductivity of PVPA is improved by compositing with PMVTri • The water resistance of PVPA is improved by compositing with PMVTri • The oxidative stability is greatly improved - Abstract: The poly(vinylphosphonic acid) (PVPA), poly(4-(α-methyl)vinyl-1H-1,2,3-triazole) (PMVTri), and poly(VPA-co-MVTri) were synthesized, and proton exchange membranes were prepared based on the acid-base polymeric composite of PVPA and PMVTri, and acid-base amphoteric copolymer of poly(VPA-co-MVTri). The overall performances of PVPA, proton conductivity, thermal and oxidative stability, and water resistance, are greatly improved by compositing of PMVTri or copolymerization with 4-(α-methyl)vinyl-1H-1,2,3-triazole (MVTri). About four or eight folds improvement in maximum proton conductivity was observed in the polymeric composite of PVPA/PMVTri or acid-base amphoteric copolymer poly(VPA-co-MVTri) because of the redistribution of ions in the heterostructures of PVPA and PMVTri, respectively, compared with the pristine PVPA. At the same time, the oxidative stability and the water resistance of PVPA were also greatly improved attributing to the absent of α-H in the main chain of PMVTri and the acid-base interaction between the phosphonic acid groups and the triazolyl groups, respectively

  16. A new nanocomposite polymer electrolyte based on poly(vinyl alcohol) incorporating hypergrafted nano-silica

    KAUST Repository

    Hu, Xian-Lei

    2012-01-01

    Solid-state nanocomposite polymer electrolytes based on poly(vinyl alcohol)(PVA) incorporating hyperbranched poly(amine-ester) (HBPAE) grafted nano-silica (denoted as SiO2-g-HBPAE) have been prepared and investigated. Through surface pretreatment of nanoparticles, followed by Michael-addition and a self-condensation process, hyperbranched poly(amine-ester) was directly polymerized from the surface of nano-silica. Then the hypergrafted nanoparticles were added to PVA matrix, and blended with lithium perchlorate via mold casting method to fabricate nanocomposite polymer electrolytes. By introducing hypergrafted nanoparticles, ionic conductivity of solid composite is improved significantly at the testing temperature. Hypergrafted nano-silica may act as solid plasticizer, promoting lithium salt dissociation in the matrix as well as improving segmental motion of matrix. In addition, tensile testing shows that such materials are soft and tough even at room temperature. From the dielectric spectra of nanocomposite polymer electrolyte as the function of temperature, it can be deduced that Arrhenius behavior appears depending on the content of hypergrafted nano-silica and concentration of lithium perchlorate. At a loading of 15 wt% hypergrafted nano-silica and 54 wt% lithium perchlorate, promising ionic conductivities of PVA nanocomposite polymer electrolyte are achieved, about 1.51 × 10 -4 S cm-1 at 25 °C and 1.36 × 10-3 S cm-1 at 100 °C. © The Royal Society of Chemistry.

  17. Adsorption of poly(vinyl formamide-co-vinyl amine) (PVFA-co-PVAm) polymers on zinc, zinc oxide, iron, and iron oxide surfaces.

    Science.gov (United States)

    Seifert, Susan; Simon, Frank; Baumann, Giesela; Hietschold, Michael; Seifert, Andreas; Spange, Stefan

    2011-12-06

    The adsorption of poly(vinyl formamide) (PVFA) and the statistic copolymers poly(vinyl formamide-co-vinyl amine) (PVFA-co-PVAm) onto zinc and iron metal particles as well as their oxides was investigated. The adsorbates were characterized by means of XPS, DRIFT spectroscopy, wet chemical analysis, and solvatochromic probes. Dicyano-bis-(1,10-phenanthroline)-iron(II) (1), 3-(4-amino-3-methylphenyl)-7-phenyl-benzo-[1,2-b:4,5-b']difuran-2,6-dione (2), and 4-tert-butyl-2-(dicyano-methylene)-5-[4-(diethylamino)-benzylidene]-Δ(3)-thiazoline (3) as solvatochromic probes were coadsorbed onto zinc oxide to measure various effects of surface polarity. The experimental findings showed that the adsorption mechanism of PVFA and PVFA-co-PVAm strongly depends on the degree of hydrolysis of PVFA and pH values and also on the kind of metal or metal oxide surfaces that were employed as adsorbents. The adsorption mechanism of PVFA/PVFA-co-PVAm onto zinc oxide and iron oxide surfaces is mainly affected by electrostatic interactions. Particularly in the region of pH 5, the adsorption of PVFA/PVFA-co-PVAm onto zinc and iron metal particles is additionally influenced by redox processes, dissolution, and complexation reactions. © 2011 American Chemical Society

  18. Blends of ethylene-co-vinyl acetate and poly(3-hydroxybutyrate with adhesion property

    Directory of Open Access Journals (Sweden)

    A. de Lucas-Freile

    2018-07-01

    Full Text Available The structure and properties of ethylene-co-vinyl acetate (EVA and poly(3-hydroxybutyrate (PHB blends depended on their PHB content, i.e. PHB phase dominated the structure for amounts of PHB higher than 50 wt%, whereas EVA phase is dominant for PHB content lower than 50 wt%. EVA/PHB (70:30 blend showed unexpected different structure because of higher miscibility and the creation of new interfacial interactions between C=O and CH3 groups of PHB and CH3 and C=O groups of EVA, these interactions led changing of the phase structure of ethylene and vinyl acetate domains in EVA. As a consequence, improved thermal, viscoelastic and morphological properties were obtained. EVA+PHB blends containing 60 wt% or more PHB did not show tack and, interestingly, the addition of 20–30 wt% PHB enhanced the tack and displaced the maximum tack of pure EVA to lower temperature. The tack of EVA/PHB (70:30 blend was the highest among all blends because of its particular structure, fibrillation was also shown. Finally, the adhesion of EVA+PHB blends containing 20–30 wt% PHB to polypropylene (PP substrate was higher than the one of pure EVA because of the interactions between the ethylene domains in EVA phase of the blend and PP substrate surface.

  19. Mechanical, relaxation behavior and thermal degradation of UV irradiated poly(vinyl acetate)/poly( methyl methacrylate) blends

    International Nuclear Information System (INIS)

    Mansour, S.A.; Hafez, M.; Hussien, K.A.

    2005-01-01

    The effect of different doses of UV- irradiation on the mechanical and relaxation properties of poly(vinyl acetate)/poly(methyl methacrylate) blends were studied. Films of PVAc/PMMA blend with different contents were prepared using the casting technique. Also, PMMA could be blended with PVAc to improve its impact strength. Moreover UV-irradiation causes degradation of PVAc and formation of ketonic and aldehyde carbonyl groups according to a suggested scheme. Irradiation of PvAc/ PMMA blends causes a higher degree of degradation as compared to the PVAc alone although the PMMA is more susceptible than PVAc to the influence of radiation. Recognizable differences are observed for all parameters between the unirradiated and irradiated samples. Existence of a relaxation mechanism within the first 200s is reported. The shear modulus for all samples is also obtained and discussed. These data are used to calculate the strain energy density using the equation proposed by Blatzetal(1974 trans. Soc.Rheol. 18 145-61), based on the n-measure of Sethe

  20. Protein valves prepared by click reaction grafting of poly(N-isopropylacrylamide) to electrospun poly(vinyl chloride) fibrous membranes

    Science.gov (United States)

    Guo, Jian-Wei; Lin, Zhen-Yu; Chang, Chi-Jung; Lu, Chien-Hsing; Chen, Jem-Kun

    2018-05-01

    In this study, poly(vinyl chloride) (PVC) was electrospun into fibrous membranes and then reacted with NaN3 to generate azido-terminated PVC fibrous membranes. A propargyl-terminated poly(N-isopropylacrylamide) (PNIPAAm) was also synthesized and then grafted, through click reactions, onto the azido-terminated PVC fiber surface. Protrusion-, scale-, and joint-like structures of the PNIPAAm grafts on the PVC fibers were formed upon increasing the molecular weight of the PNIPAAm grafts. The PNIPAAm-grafted PVC fibrous mats exhibited completely wetted surfaces at 25 °C because of their high roughness. The static water contact angle of the PNIPAAm-grafted PVC fibrous mats reached 140° when the temperature was increased to 45 °C. This thermoresponsive behavior was significantly greater than that of the PNIPAAm grafted on a flat surface. Temperature-responsive membranes were constructed having a pore size of 1.38 μm and applied as protein valves to block and release an antibody (fluorescein-conjugated AffiniPure goat anti-rabbit IgG). At 25 °C, the collection efficiency remained at 94% for antibody concentrations up to 60 ng/L. As the temperature increased to 45 °C, the collection efficiency decreased abruptly, to 4%, when the antibody concentration was greater than 20 ng/L. Accordingly, this system of PNIPAAm-grafted PVC fibers functioned as a protein valve allowing the capture and concentration of proteins.

  1. Electron Beam Damage in Poly(Vinyl Chloride) and Poly(Acrylonitrile) as Observed by Auger Electron Spectroscopy

    International Nuclear Information System (INIS)

    Lea, Alan S.; Engelhard, Mark H.; Baer, Donald R.

    2003-01-01

    AES spectra of spun-cast films of poly(vinyl chloride) (PVC) and poly(acrylonitrile) (PAN) were collected over a period of time to determine specimen damage during exposure to a 10kV electron beam. For the PVC, loss of chlorine was observed over a period of 203 minutes to the extent that the final chlorine concentration was only 20% of its original value. PAN exhibited a loss in nitrogen content over a period of 120 minutes, but the rate of damage to the polymer was significantly less than PVC. Figure 1 shows the atomic concentration in the PVC film as a function of dose (time). It takes a dose of approximately 7.0x10-5 Ccm-5 for the chlorine concentration to fall from its original value by 10% (one definition of critical dose). Figure 2 shows a similar drop in nitrogen concentration in the PAN film as a function of dose. For this polymer, it takes a dose of 1.3x10-3 Ccm-2 for the nitrogen concentration to fall by 10%

  2. Tunable shape memory behaviors of poly(ethylene vinyl acetate) achieved by adding poly(L-lactide)

    International Nuclear Information System (INIS)

    Zhang, Zhi-xing; Liao, Fei; He, Zhen-zhen; Yang, Jing-hui; Huang, Ting; Zhang, Nan; Wang, Yong; Gao, Xiao-ling

    2015-01-01

    In this work, different contents of poly(L-lactide) (PLLA) (20–50 wt%) were introduced into poly(ethylene vinyl acetate) (EVA) to prepare the samples with a tunable shape memory behavior. Morphological characterization demonstrated that with increasing PLLA content from 20 to 50 wt%, the blend morphology changed from sea-island structure to cocontinuous structure. In all the samples, PLLA was amorphous and it did not affect the crystallization of polyethylene part in the EVA component. The presence of PLLA greatly enhanced the storage modulus of samples, especially at relatively low temperatures. The shape memory behaviors of samples were systematically investigated and the results demonstrated that the EVA/PLLA blends exhibited a tunable shape memory effect. On one hand, PLLA accelerated the shape fixation and enhanced the fixity ratio of samples. On the other hand, PLLA reduced the dependence of shape fixity of samples on fixity temperatures. Specifically, for the first time, a critical recovery temperature was observed for the immiscible shape memory polymer blends. In this work, the critical recovery temperature was about 53 °C. At recovery temperature below the critical value, the blends exhibited smaller recovery ratios compared with the pure EVA, however, at recovery temperature above 53 °C, the blends exhibited higher recovery ratios. (paper)

  3. A study of poly(vinyl alcohol thermal degradation by thermogravimetry and differential thermogravimetry

    Directory of Open Access Journals (Sweden)

    Julián Esteban Barrera

    2007-05-01

    Full Text Available The thermal degradation of poly(vinyl alcohol (PVA having different degrees of hydrolysis and molecular weights was studied by thermogravimetry (TGA and differential thermogravimetry (DTGA. Four degradation events were identified whose intensity was related to the degree of hydrolysis. It was verified that the solid-state degradation mechanism for high hydrolysis degrees corresponded to eliminating water-forming side groups in stoichiometric amounts. The presence of acetate groups and lower melting points delayed the polymer’s thermal decomposition at lower hydrolysis degrees. There was no direct correlation in these samples between weight-loss during the first degradation event and the stoichiometric quantities which would be produced by eliminating the side groups. Reaction order and energy activation value qualitative coincidence was found by evaluating experimental data by using Freeman-Carroll and Friedman kinetic models.

  4. Sliding friction at poly(vinyl alcohol)-modified carbon nanotube interfaces

    Science.gov (United States)

    Zhang, Xiaohua

    2018-01-01

    The sliding friction between adjacent carbon nanotubes (CNTs) determines greatly the mechanical property of CNT assembly materials. In order to enhance the intertube friction, polymer molecules are often introduced between CNTs. This paper reveals a new energy dissipation mechanism for the deformed CNT contacts by poly(vinyl alcohol) (PVA). When PVA is introduced into a CNT bundle, most segments of the polymer chain lay on the grooves of adjacent CNTs, while several short segments span over the contact CNTs by inducing a structural deformation on the tubular structure. During the tube sliding, the deformation is recovered and a new one is formed at the next position, contributing to new energy dissipation to prevent the tube sliding. As a result, the friction force can be enhanced by up to eight-fold. This study indicates that a network of transverse polymer chains and longitudinal CNTs is important towards high mechanical properties.

  5. Electro–optical properties of poly(vinyl acetate)/polyindole composite film

    International Nuclear Information System (INIS)

    Bhagat, D. J.; Dhokane, G. R.; Bajaj, N. S.

    2016-01-01

    In present work, electrical and optical properties of poly(vinyl acetate)/polyindole (PVAc/PIN) composite film are reported. The prepared composite was characterized via X–ray diffraction (XRD), UV–Vis spectroscopy and DC conductivity measurements. The polymer chain separation was determined using XRD analysis. An attempt has been made to study the temperature dependence of DC conductivity of PVAc/PIN composite in temperature range 308–373 K. The DC conductivity initially increases and reaches to 2.45×10–7 S/cm. The optical band gap value of composite is determined as 4.77 eV. The semiconducting nature of composite observed from electronic as well as optical band gap and Arrhenius behavior of DC plot.

  6. Dynamic mechanical properties of photopolymerizable poly(vinyl alcohol)-acrylate monomer blends

    International Nuclear Information System (INIS)

    Koshiba, M.; Yamaoka, T.; Tsunoda, T.

    1983-01-01

    Dynamic mechanical properties of photopolymerizable poly(vinyl alcohol) (PVA)-monoacrylate blends were investigated by measuring dynamic shear modulus G' and loss tangent, tan delta. The dynamic mechanical properties of the blends before being exposed to UV irradiation were governed by the weight percent of the monomers which act as plasticizers. On the other hand, the UV-irradiated blends seemed to be typical two-phase materials since they revealed two tan delta maxima whose positions were independent of the monomer content. Those two maxima were assigned to PVA and photopolymerized acrylates with reference to the dynamic mechanical data of PVA and a PVA-polyacrylamide polyblend. Those dynamic mechanical data suggested that insolubilization of the blend type photopolymers should be caused by a decrease in solubility due to graft polymerization of acrylate monomers onto PVA. 9 figures, 3 tables

  7. PREPARATION AND CHARACTERIZATION OF COMPOSITES COMPRISING MODIFIED HARDWOOD AND WOOD POLYMERS/POLY(VINYL CHLORIDE

    Directory of Open Access Journals (Sweden)

    Ruxanda Bodîrlău

    Full Text Available Chemical modification of hardwood sawdust from ash-tree species was carried out with a solution of maleic anhydride in acetone. Wood polymers, lignin, and cellulose were isolated from the wood sawdust and modified by the same method. Samples were characterized by Fourier transform infrared spectroscopy (FTIR, providing evidence that maleic anhydride esterifies the free hydroxyl groups of the wood polymer components. Composites comprising chemically modified wood sawdust and wood polymers (cellulose, lignin-as variable weight percentages-, and poly (vinyl chloride were obtained and further characterized by using FTIR spectroscopy and scanning electron microscopy (SEM. The thermal behavior of composites was investigated by using the thermogravimetric analysis (TGA. In all cases, thermal properties were affected by fillers addition.

  8. Gamma irradiation Effect on the Non-Crosslinked and Crosslinked Poly(vinyl alcohol) Films

    International Nuclear Information System (INIS)

    El-Sawy, N.M.; El-Arnaouty, M.B.; Abdel Ghaffar, A.M.

    2008-01-01

    The non-crosslinked and crosslinked poly(vinyl alcohol) (PVA) films were prepared by the cast method then irradiated with gamma rays for various doses up to 300 kGy. The structure and characterization of PVA were determined by using Infrared spectroscopy (FTIR), ultraviolet spectroscopy (UV). Swelling behaviour was also investigated. Mechanical properties have been examined with respect to the absorbed dose. The color of the films changed to yellowish-white after irradiation. Additional changes were observed using FTIR analysis on the degradation products demonstrated that the radiolysis of PVA was initiated by liberation of H and OH groups leading to scission of the main chains and formation of carbonyl and double bond groups. Thermogravimetric analysis (TGA) was performed

  9. Dehydration driven changes in the structure and mechanical behavior of electrospun poly (vinyl alcohol) nanofibers

    International Nuclear Information System (INIS)

    Bansal, Ankita; Sinha, Arvind

    2012-01-01

    Electrospun nanofibers of poly (vinyl alcohol) (PVA) are well known for their possible application in different fields, ranging from packaging to tissue engineering. However, biomedical application of these nanofibers gets limited due to its rapid disintegration in water, causing mechanical instability. Addressing this issue, the present manuscript reports ethanol induced dehydration of electrospun PVA nanofibers, and its effects on the structure and mechanical properties of the electrospun system. A systematic variation in the structure and mechanical stability of nanofibers as a function of PVA concentration has also been established in the both hydrated and dehydrated states. - Highlights: ► Study reports structure-property correlation of dehydrated PVA nanofibers. ► Results confirm symmetrical reversal of properties in two states. ► Experimental results are in confirmation with the fusion model of nanofibers.

  10. Preparation and study of poly vinyl alcohol/hyperbranched polylysine fluorescence fibers via wet spinning

    Science.gov (United States)

    Lu, Hongwei; Zou, Liming; Xu, Yongjing; Sun, Hong; Li, Yan Vivian

    2018-02-01

    A simple method of using wet spinning was found effective in the preparation of photoluminescent poly vinyl alcohol (PVA)/hyperbranched polylysine (HBPL) fibers. The photoluminescence of the PVA/HBPL fibers was significantly uniform and the unique uniformity was obtained by controlling the mass ratio of PVA to HBPL in aqueous solutions used in the wet spinning process. The high solubility of HBPL in water make it feasible to well control in the mass ratio of PVA to HBPL, which facilitated the formation of a unique PVA/HBPL mixture, resulting in the fabrication of homogeneous PVA composite fluorescence fibers. The composite fibers exhibit good mechanical, and thermal properties that make the PVA/HBPL fluorescent fibers a great material potentially used in fluorescence applications including optics, imaging and detection.

  11. Effect of Electron Beam Irradiation on the Structure and Optical Properties of Poly (vinyl alcohol)

    International Nuclear Information System (INIS)

    Abutalib, M.M.

    2011-01-01

    Samples from of the polymeric material poly (vinyl alcohol) PVA have been exposed to electron beam in the dose range 5-100 kGy. The modifications induced in PVA samples due to electron beam irradiation have been studied through different characterization techniques such as X-ray diffraction XRD, Fourier Transform Infrared spectroscopy FTIR and color difference studies. The FTIR spectroscopy indicated that the degradation is the dominant mechanism at the dose range 5-60 kGy. Above 60 and up to 100 kGy, crosslinking is achieved. The crosslinking reported by FTIR spectroscopy destroyed the degree of ordering in the PVA samples as revealed by XRD. Additionally, the non irradiated PVA samples showed significant color sensitivity towards electron beam irradiation that appeared in the increase of the green and blue color components. This was accompanied by a net increase in the darkness of the samples

  12. Mechanical and dielectric properties of carbon nanotubes/poly (vinyl alcohol) nanocomposites

    Science.gov (United States)

    Amrin, Sayed; Deshpande, V. D.

    2016-05-01

    In this work, two series of nanocomposites of poly(vinyl alcohol) (PVA) incorporated with multiwalled carbon nanotubes (MWNT) and carboxyl functionalized multiwalled carbon nanotubes (MWNT-COOH) were fabricated using solution-cast method and their tensile and dielectric properties were studied. Tensile tests were carried out on composite films of MWNT/PVA and MWNT-COOH/PVA for different loading levels. Results show that overall mechanical properties of the MWNT-COOH/PVA composite was greatly improved as compared to the MWNT/PVA film. The dielectric properties of nanocomposites were investigated in a frequency range from 0.1Hz to 10MHz at room temperature respectively. Compared to MWNT/PVA composites, higher dielectric constant and ac conductivity was achieved in MWNT-COOH/PVA nanocomposite, which can be well explained by the interfacial polarization effect.

  13. Crosslinked poly(vinyl alcohol hydrogels for wound dressing applications: A review of remarkably blended polymers

    Directory of Open Access Journals (Sweden)

    Elbadawy A. Kamoun

    2015-01-01

    Full Text Available A series of excellent poly(vinyl alcohol (PVA/polymers blend hydrogel were reviewed using different crosslinking types to obtain proper polymeric dressing materials, which have satisfied biocompatibility and sufficient mechanical properties. The importance of biodegradable–biocompatible synthetic polymers such as PVA, natural polymers such as alginate, starch, and chitosan or their derivatives has grown significantly over the last two decades due to their renewable and desirable biological properties. The properties of these polymers for pharmaceutical and biomedical application needs have attracted much attention. Thus, a considered proportion of the population need those polymeric medical applications for drug delivery, wound dressing, artificial cartilage materials, and other medical purposes, where the pressure on alternative polymeric devices in all countries became substantial. The review explores different polymers which have been blended previously in the literature with PVA as wound dressing blended with other polymeric materials, showing the feasibility, property change, and purpose which are behind the blending process with PVA.

  14. Fabrication of α-chitin whisker-reinforced poly(vinyl alcohol) nanocomposite nanofibres by electrospinning

    International Nuclear Information System (INIS)

    Junkasem, Jirawut; Rujiravanit, Ratana; Supaphol, Pitt

    2006-01-01

    The present contribution reports, for the first time, the successful fabrication of α-chitin whisker-reinforced poly(vinyl alcohol) (PVA) nanocomposite nanofibres by electrospinning. The α-chitin whiskers were prepared from α-chitin flakes from shrimp shells by acid hydrolysis. The as-prepared chitin whiskers exhibited lengths in the range 231-969 nm and widths in the range 12-65 nm, with the average length and width being about 549 and 31 nm, respectively. Successful incorporation of the chitin whiskers within the as-spun PVA/chitin whisker nanocomposite nanofibres was verified by infrared spectroscopic and thermogravimetric methods. The incorporation of chitin whiskers within the as-spun nanocomposite fibre mats increased the Young's modulus by about 4-8 times over that of the neat as-spun PVA fibre mat

  15. Effects of poly-vinyl alcohol on supercooling phenomena of water

    Energy Technology Data Exchange (ETDEWEB)

    Kumano, Hiroyuki; Hirata, Tetsuo; Kudoh, Tomoya [Department of Mechanical Systems Engineering, Shinshu University, 4-17-1, Wakasato, Nagano City, 380-8553 (Japan)

    2009-05-15

    The effects of a polymer additive on the supercooling of water were investigated experimentally. Poly-vinyl alcohols (PVAs) were used as the additives, and samples were prepared by dissolving the PVA in water. Since the characteristics of PVA are decided by its degrees of polymerization and saponification, these were varied along with the concentration as the experimental parameters. Moreover, the effect of purity of the water was also considered. Each sample was cooled and the temperature at the instant when ice appeared was measured. Since the freezing of supercooled water is a statistical phenomenon, many experiments were carried out and the average degree of supercooling was obtained. It was found that PVA affects the nucleation of ice in supercooled water and the degree of supercooling increases with the addition of PVA even for water with low purity. The average degree of supercooling increases with an increase in the degree of saponification of PVA. (author)

  16. Dynamics in poly vinyl alcohol (PVA) based hydrogel: Neutron scattering study

    Energy Technology Data Exchange (ETDEWEB)

    Prabhudesai, S. A., E-mail: swapnil@barc.gov.in; Mitra, S.; Mukhopadhyay, R. [Solid State Physics Division, Bhabha Atomic Research Centre, Mumbai 40085 (India); Lawrence, Mathias B. [Department of Physics, St. Xavier’s College, Mapusa, Goa 403507 (India); Desa, J. A. E. [Department of Physics, Goa University, Taleigao Plateau, Goa 403206 (India)

    2015-06-24

    Results of quasielastic neutron scattering measurements carried out on Poly Vinyl Alcohol (PVA) based hydrogels are reported here. PVA hydrogels are formed using Borax as a cross-linking agent in D{sub 2}O solvent. This synthetic polymer can be used for obtaining the hydrogels with potential use in the field of biomaterials. The aim of this paper is to study the dynamics of polymer chain in the hydrogel since it is known that polymer mobility influences the kinetics of loading and release of drugs. It is found that the dynamics of hydrogen atoms in the polymer chain could be described by a model where the diffusion of hydrogen atoms is limited within a spherical volume of radius 3.3 Å. Average diffusivity estimated from the behavior of quasielastic width is found to be 1.2 × 10{sup −5} cm{sup 2}/sec.

  17. Properties of poly(vinyl alcohol)-borax gel doped with neodymium and praseodymium

    International Nuclear Information System (INIS)

    Lawrence, Mathias B.; Desa, J.A.E.; Rai, Renu; Aswal, V.K.

    2014-01-01

    Neodymium and praseodymium ions, singly and in combination, have been doped into a poly(vinyl alcohol)-borax matrix. X-ray diffraction shows structural correlations from 2 to 6 Å and 15 Å, while small angle neutron scattering indicates that the rare-earth ions do not affect the nanoscale structures of the gels. Differential scanning calorimetry shows the glass transition temperature to increase with concentration of Pr in the gel. Excitation in the ultraviolet region leads to luminescent emission in the visible region. Simultaneous absorption in the visible region then leads to luminescent emission in the near infra-red region. The spectral qualities of the emission bands can be varied by choosing appropriate relative ratios of rare-earth species. (author)

  18. Electro–optical properties of poly(vinyl acetate)/polyindole composite film

    Energy Technology Data Exchange (ETDEWEB)

    Bhagat, D. J., E-mail: bhagatd@rediffmail.com; Dhokane, G. R. [Arts, Science and Commerce College, Chikhaldara, 444807, Maharashtra (India); Bajaj, N. S. [Toshniwal Arts, Science and Commerce College, Sengaon, Maharashtra (India)

    2016-05-06

    In present work, electrical and optical properties of poly(vinyl acetate)/polyindole (PVAc/PIN) composite film are reported. The prepared composite was characterized via X–ray diffraction (XRD), UV–Vis spectroscopy and DC conductivity measurements. The polymer chain separation was determined using XRD analysis. An attempt has been made to study the temperature dependence of DC conductivity of PVAc/PIN composite in temperature range 308–373 K. The DC conductivity initially increases and reaches to 2.45×10–7 S/cm. The optical band gap value of composite is determined as 4.77 eV. The semiconducting nature of composite observed from electronic as well as optical band gap and Arrhenius behavior of DC plot.

  19. Polyurethane/poly(vinyl alcohol hydrogel coating improves the cytocompatibility of neural electrodes

    Directory of Open Access Journals (Sweden)

    Mei Li

    2015-01-01

    Full Text Available Neural electrodes, the core component of neural prostheses, are usually encapsulated in polydimethylsiloxane (PDMS. However, PDMS can generate a tissue response after implantation. Based on the physicochemical properties and excellent biocompatibility of polyurethane (PU and poly(vinyl alcohol (PVA when used as coating materials, we synthesized PU/PVA hydrogel coatings and coated the surface of PDMS using plasma treatment, and the cytocompatibility to rat pheochromocytoma (PC12 cells was assessed. Protein adsorption tests indicated that the amount of protein adsorption onto the PDMS substrate was reduced by 92% after coating with the hydrogel. Moreover, the PC12 cells on the PU/PVA-coated PDMS showed higher cell density and longer and more numerous neurites than those on the uncoated PDMS. These results indicate that the PU/PVA hydrogel is cytocompatible and a promising coating material for neural electrodes to improve their biocompatibility.

  20. Poly(vinyl chloride-grafted multi-walled carbon nanotubes via Friedel-Crafts alkylation

    Directory of Open Access Journals (Sweden)

    2010-11-01

    Full Text Available A novel approach was developed for the surface modification of the multi-walled carbon nanotubes (MWCNTs with high percentage of grafting (PG% by the grafting of polymer via the Friedel-Crafts alkylation. The graft reaction conditions, such as the amount of catalyst added, the reaction temperature, and the reaction time were optimized for the Friedel-Crafts alkylation of the MWCNTs with poly(vinyl chloride (PVC with anhydrous aluminum chloride (AlCl3 as catalyst in chloroform (CHCl3. The Fourier Transform Infrared (FT-IR, Raman, and thermogravimetric (TGA analysis showed that PVC had been successfully grafted onto MWCNTs both at the ends and on the sidewalls by the proposed Friedel-Crafts alkylation. The PVC grafted MWCNTs (PVC-MWCNTs could be dispersed well in organic solvent and the dispersion was more stable.

  1. Fabrication and Characterization of Electrospun Wool Keratin/Poly(vinyl alcohol Blend Nanofibers

    Directory of Open Access Journals (Sweden)

    Shuai Li

    2014-01-01

    Full Text Available Wool keratin/poly(vinyl alcohol (PVA blend nanofibers were fabricated using the electrospinning method in formic acid solutions with different weight ratios of keratin to PVA. The resultant blend nanofibers were characterized by scanning electron microscopy (SEM, Fourier transform infrared (FTIR, X-ray diffraction (XRD, thermal gravimetric analysis (TGA, and tensile test. SEM images showed that the diameter of the blend nanofibers was affected by the content of keratin in blend solution. FTIR and XRD analyses data demonstrated that there were good interactions between keratin and PVA in the blended nanofibers caused by possibly hydrogen bonds. The TGA study revealed that the thermal stability of the blend nanofibers was between those of keratin and PVA. Tensile test indicated that the addition of PVA was able to improve the mechanical properties of the electrospun nanofibers.

  2. Compatibilizing role of carbon nanotubes in poly(vinyl alcohol)/starch blend

    KAUST Repository

    Jose, Jobin Vinodh

    2014-10-03

    Polymer nanocomposites based on poly(vinyl alcohol)/starch blend and carbon nanotubes (CNT) were prepared by solution mixing, followed by casting. Glycerol was used as a plasticizer and added in the starch dispersion. The uniform dispersion of CNT in water before mixing with PVA/starch blend, was achieved by using an Ultrasonicator probe. The composites were characterized by measurement of tensile properties, thermal analysis, FE-SEM, TEM, XRD studies, and water uptake. It was observed that the decrease in tensile strength, modulus, and elongation at break on addition of starch into PVA can be arrested by incorporation of CNT. The strong physical bonding such as hydrogen bonding among the hydroxyl groups of polymer components and oxygen containing groups on CNT surface resulted in a more tortuous path for the water to follow, lowering of water uptake. Thermal analysis and spectroscopic images showed an increase in blend homogeneity in the presence of CNT.

  3. Novel synthesis on poly (vinyl alcohol): characterization, complexation a biological activity

    International Nuclear Information System (INIS)

    El-Sawy, N.M.; Elassar, A.Z.; Al-Fulaij, O.

    2002-01-01

    Poly(vinyl alcohol), PVA, readily condensed with phenyl hydrazine and malononitrile in basic medium to give the hydrazone and pyran derivatives, respectively. PVA reacted with chloroacetonitrile, biuet and thiophene carbonyl chloride to give modified polymeric materials. While addition of PVA to acrylonitrile and phenyl isothiocyanate gives the ether and thiocarbamate ester derivatives, respectively. Hydroxylamine hydrochloride reacted with the modified, carbonitrile containing, polymer to give the amidoxime derivative. The amidoximated products of PVA and carbamate ester of polymeric material were complexed with CUCL2 solution. The complex materials were confirmed by using UV and ESDS measurements. The morphology of PVA and complex with CUII was observed by SEM. Biological activity of some of the prepared compounds was investigated toward bacteria and fungi

  4. Birefringence and dichroism of poly(vinyl-alcohol) foils containing phthalazinium ylids

    Science.gov (United States)

    Rogojanu, Alina; Dascalu, Carmen Felicia; Zelinschi, Beatrice Carmen; Caprosu, Maria; Dorohoi, Dana Ortansa

    2011-10-01

    Pure and colored with phthalazinium ylids poly(vinyl-alcohol) (PVA) foils were stretched under gentile heating. The birefringence of the thin foils was determined with a Babinet compensator standardized for yellow radiation of a Sodium lamp. The determined birefringence of the colored PVA foils is higher than that of the pure PVA foils. This fact indicates that the phthalazinium ylids facilitate the increase in the anisotropy of the stretched foils. The visible absorption electronic band of phthalazinium ylids was used to estimate the dichroic ratio and the degree of order of the ylid molecules in the stretched PVA foils. An increase in dichroism and birefringence with the degree of stretching has been evidenced for uncolored and colored PVA foils.

  5. Permanent hydrophilic modification of polypropylene and poly(vinyl alcohol) films by vacuum ultraviolet radiation

    Energy Technology Data Exchange (ETDEWEB)

    Belmonte, Guilherme Kretzmann [Instituto de Química, Universidade Federal do Rio Grande do Sul (UFRGS), Avenida Bento Gonçalves 9500, 91501-970 Porto Alegre, RS (Brazil); Charles, German [Centro de Química Aplicada (CEQUIMAP), Facultad de Ciencias Químicas, Unversidad Nacional de Córdoba, Haya de la Torre y Medina Allende, Edificio de Ciencias II, Ciudad Universitaria, Córdoba 5000 (Argentina); Strumia, Miriam Cristina [Departamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, IPQA-Conicet, Haya de la Torre y Medina Allende, Edificio de Ciencias II, Ciudad Universitaria, Córdoba 5000 (Argentina); Weibel, Daniel Eduardo, E-mail: danielw@iq.ufrgs.br [Instituto de Química, Universidade Federal do Rio Grande do Sul (UFRGS), Avenida Bento Gonçalves 9500, 91501-970 Porto Alegre, RS (Brazil)

    2016-09-30

    Highlights: • Polypropylene and Poly(vinyl alcohol) were surface modified by vacuum ultraviolet (VUV) irradiation. • The hydrophilicity of the treated films was permanent and resisted aging for several months. • Grafting of styrene monomer was only observed in the VUV irradiated regions. • The obtained results showed the potential in the use of VUV treatment for surface modification and processing of polymers which lack chromophores in the UV region. - Abstract: Polypropylene (PP) and Poly(vinyl alcohol) (PVA) both synthetics polymers but one of them biodegradable, were surface modified by vacuum ultraviolet (VUV) irradiation. After VUV irradiation in an inert nitrogen atmosphere, the films were exposed to oxygen gas. The treated films were characterized by water contact angle measurements (WCA), optical profilometry, FTIR-ATR, XPS, UPS and NEXAFS techniques. PP and PVA VUV-treated films reached superhydrophilic conditions (WCAs <10°) in about 30 min of irradiation under our experimental conditions. It was observed that when the WCAs reached about 35–40° the hydrophilicity was permanent in both polymers. These results contrasted with typical plasma treatments were a rapid hydrophobic recovery with aging time is usually observed. UPS and XPS data showed the presence of new functionalities on the PP and PVA surfaces that were assigned to COO, C=O, C−O and C=C functional groups. Finally, grafting of styrene (ST) as a typical monomer was tested on PP films. It was confirmed that only in the VUV irradiated region an efficient grafting of ST or polymerized ST was found. Outside the irradiated regions no ST grafted was observed. Our results showed the potential use of VUV treatment for surface modification and processing of polymers which lack chromophores in the UV region.

  6. The characterization of wound dressing poly (vinyl pyrrolidone) hydrogels using gamma radiation

    Energy Technology Data Exchange (ETDEWEB)

    Rezende, Talita C.; Pinheiro, Christiano J.G., E-mail: talitacolombi@yahoo.com, E-mail: christrieste@yahoo.it [Universidade Federal do Espirito Santo (CCA/UFES), Alegre, ES (Brazil). Programa de Pós-Graduação em Engenharia Química; Paula, Heberth D., E-mail: hdpaula@gmail.com [Universidade Federal do Espirito Santo, Alegre (UFES), ES (Brazil). Departamento de Farmácia; Morais, Pedro A.B., E-mail: pedmora2005@gmail.com [Universidade Federal do Espirito Santo (UFES), Alegre, ES (Brazil). Departamento de Química

    2017-07-01

    The first hydrogel for wound dressing processed by radiation was developed in Poland in 1986 by the inventor Janusz M. Rosiak and reached the local market in 1992. Laboratories of developing countries, which face all kinds of restrictions, were seduced by the simplicity of the process and low cost of its raw materials. It was a technological breakthrough due to its painless product characteristics and having improved healing properties such as absorbing a high water capacity, attached to healthy skin, and being easy to remove, plus its intelligent production process combining sterilization and crosslinking in a simultaneous operation. The use of hydrogels as biomaterials has increased recently. Hydrogel wound dressings were prepared using the gamma ray irradiation technique. Radiation was applied as a tool for crosslinking and sterilization of these materials. The hydrogels are composed of poly (N-vinyl-2-pyrrolidone) (PVP), poly (ethylene glycol) (PEG) and agar at radiation doses of 15, 20, 25, 30 kGy. The influence of some process parameters on their properties was investigated by: sterilization, gel fraction, swelling measures and mechanical properties. Hydrogels with less than 20 kGy of radiation were not properly sterilized. The gel fraction and swelling increased with increasing radiation dose due to increased crosslinking density, and at 25kGy, obtained optimum swelling. No significant differences were found for the test of mechanical properties but hydrogel matrices of different doses of gamma radiation. (author)

  7. Enhancement of conductivity in polyaniline-[poly(vinylidene chloride)-co-(vinyl acetate)] blends by irradiation

    International Nuclear Information System (INIS)

    Bodugoez-Sentuerk, Hatice; Gueven, Olgun

    2011-01-01

    In this study we have prepared conductive poly(aniline), (PANI) blends with poly(vinylidene chloride-co-vinyl acetate), [P(VDC-co-VAc)] copolymer with varying compositions using gamma radiation to induce conductivity. A number of blends with different compositions were prepared by solution casting followed by irradiation in a 60 Co gamma cell to different doses up to 800 kGy. Electrical conductivity of the blends was measured before and after irradiation using a four-probe technique. Increasing radiation dose resulted in an increase of 9 orders of magnitude in the conductivity of P(VDC-co-VAc)/(PANI) films reaching 0.1 S/cm at 500 kGy and beyond this dose a decrease was observed. Effect of film thickness on conductivity of the blends was investigated and a slight increase of an order of magnitude was observed on increasing the film thickness from 50 to 200 μm. It was also observed that PANI blends exhibited a stretch dependent small increase in conductivity. The conductivity of the irradiated films was found to be stable for up to 12 months under ambient conditions.

  8. In vivo evaluation of the bone integration of coated poly(vinyl-alcohol) hydrogel fiber implants.

    Science.gov (United States)

    Moreau, David; Villain, Arthur; Bachy, Manon; Proudhon, Henry; Ku, David N; Hannouche, Didier; Petite, Hervé; Corté, Laurent

    2017-08-01

    Recently, it has been shown that constructs of poly(vinyl alcohol) (PVA) hydrogel fibers reproduce closely the tensile behavior of ligaments. However, the biological response to these systems has not been explored yet. Here, we report the first in vivo evaluation of these implants and focus on the integration in bone, using a rabbit model of bone tunnel healing. Implants consisted in bundles of PVA hydrogel fibers embedded in a PVA hydrogel matrix. Half of the samples were coated with a composite coating of hydroxyapatite (HA) particles embedded in PVA hydrogel. The biological integration was evaluated at 6 weeks using histology and micro-CT imaging. For all implants, a good biological tolerance and growth of new bone tissue are reported. All the implants were surrounded by a fibrous layer comparable to what was previously observed for poly(ethylene terephthalate) (PET) fibers currently used in humans for ligament reconstruction. An image analysis method is proposed to quantify the thickness of this fibrous capsule. Implants coated with HA were not significantly osteoconductive, which can be attributed to the slow dissolution of the selected hydroxyapatite. Overall, these results confirm the relevance of PVA hydrogel fibers for ligament reconstruction and adjustments are proposed to enhance its osseointegration.

  9. Integrated antifouling and bactericidal polymer membranes through bioinspired polydopamine/poly(N-vinyl pyrrolidone) coating

    International Nuclear Information System (INIS)

    Wang, Xianghong; Yuan, Shuaishuai; Shi, Dean; Yang, Yingkui; Jiang, Tao; Yan, Shunjie; Shi, Hengchong; Luan, Shifang; Yin, Jinghua

    2016-01-01

    Graphical abstract: - Highlights: • Antifouling and bactericidal capabilities were facilely integrated into a surface via bioinspired coating. • The modification technique was very facile and universal to different types of substrate materials. • The integrated antifouling and bactericidal surfaces have great potential in wound dressing applications. - Abstract: Polypropylene (PP) non-woven has been widely used as wound dressing; however, the hydrophobic nature of PP can initiate bacterial attachment and subsequent biofilm formation. Herein, we propose a facile approach to functionalize PP non-woven with poly(ethylene glycol) (PEG) and poly(N-vinyl pyrrolidone)-iodine complex (PVP-I). PVP and PEG were successively tethered onto PP non-woven surface via versatile bioinspired dopamine (DA) chemistry, followed by complexing iodine with PVP moieties. It was demonstrated through the field emission scanning electron microscope (SEM) and spread plate method that the as-modified PP non-woven integrated both antifouling property of PEG for suppressing bacterial adhesion, and bactericidal property of PVP-I for killing the few adherent bacteria. Meanwhile, it could greatly resist platelet and red blood cell adhesion. The integrated antifouling and bactericidal PP non-woven surfaces might have great potential in various wound dressing applications.

  10. Improvement of Polylactide Properties through Cellulose Nanocrystals Embedded in Poly(Vinyl Alcohol) Electrospun Nanofibers.

    Science.gov (United States)

    López de Dicastillo, Carol; Garrido, Luan; Alvarado, Nancy; Romero, Julio; Palma, Juan Luis; Galotto, Maria Jose

    2017-05-11

    Electrospun nanofibers of poly (vinyl alcohol) (PV) were obtained to improve dispersion of cellulose nanocrystals (CNC) within hydrophobic biopolymeric matrices, such as poly(lactic acid) (PLA). Electrospun nanofibers (PV/CNC) n were successfully obtained with a final concentration of 23% ( w / w ) of CNC. Morphological, structural and thermal properties of developed CNC and electrospun nanofibers were characterized. X-ray diffraction and thermal analysis revealed that the crystallinity of PV was reduced by the electrospinning process, and the incorporation of CNC increased the thermal stability of biodegradable nanofibers. Interactions between CNC and PV polymer also enhanced the thermal stability of CNC and improved the dispersion of CNC within the PLA matrix. PLA materials with CNC lyophilized were also casted in order to compare the properties with materials based on CNC containing nanofibers. Nanofibers and CNC were incorporated into PLA at three concentrations: 0.5%, 1% and 3% (CNC respect to polymer weight) and nanocomposites were fully characterized. Overall, nanofibers containing CNC positively modified the physical properties of PLA materials, such as the crystallinity degree of PLA which was greatly enhanced. Specifically, materials with 1% nanofiber 1PLA(PV/CNC) n presented highest improvements related to mechanical and barrier properties; elongation at break was enhanced almost four times and the permeation of oxygen was reduced by approximately 30%.

  11. The characterization of wound dressing poly (vinyl pyrrolidone) hydrogels using gamma radiation

    International Nuclear Information System (INIS)

    Rezende, Talita C.; Pinheiro, Christiano J.G.; Paula, Heberth D.; Morais, Pedro A.B.

    2017-01-01

    The first hydrogel for wound dressing processed by radiation was developed in Poland in 1986 by the inventor Janusz M. Rosiak and reached the local market in 1992. Laboratories of developing countries, which face all kinds of restrictions, were seduced by the simplicity of the process and low cost of its raw materials. It was a technological breakthrough due to its painless product characteristics and having improved healing properties such as absorbing a high water capacity, attached to healthy skin, and being easy to remove, plus its intelligent production process combining sterilization and crosslinking in a simultaneous operation. The use of hydrogels as biomaterials has increased recently. Hydrogel wound dressings were prepared using the gamma ray irradiation technique. Radiation was applied as a tool for crosslinking and sterilization of these materials. The hydrogels are composed of poly (N-vinyl-2-pyrrolidone) (PVP), poly (ethylene glycol) (PEG) and agar at radiation doses of 15, 20, 25, 30 kGy. The influence of some process parameters on their properties was investigated by: sterilization, gel fraction, swelling measures and mechanical properties. Hydrogels with less than 20 kGy of radiation were not properly sterilized. The gel fraction and swelling increased with increasing radiation dose due to increased crosslinking density, and at 25kGy, obtained optimum swelling. No significant differences were found for the test of mechanical properties but hydrogel matrices of different doses of gamma radiation. (author)

  12. Integrated antifouling and bactericidal polymer membranes through bioinspired polydopamine/poly(N-vinyl pyrrolidone) coating

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xianghong [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Ministry of Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Faculty of Materials Science and Engineering, Hubei University, Wuhan 430062 (China); Yuan, Shuaishuai [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Shi, Dean, E-mail: deanshi2012@yahoo.com [Ministry of Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Faculty of Materials Science and Engineering, Hubei University, Wuhan 430062 (China); Yang, Yingkui; Jiang, Tao [Ministry of Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Faculty of Materials Science and Engineering, Hubei University, Wuhan 430062 (China); Yan, Shunjie; Shi, Hengchong [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Luan, Shifang, E-mail: sfluan@ciac.ac.cn [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Yin, Jinghua [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China)

    2016-07-01

    Graphical abstract: - Highlights: • Antifouling and bactericidal capabilities were facilely integrated into a surface via bioinspired coating. • The modification technique was very facile and universal to different types of substrate materials. • The integrated antifouling and bactericidal surfaces have great potential in wound dressing applications. - Abstract: Polypropylene (PP) non-woven has been widely used as wound dressing; however, the hydrophobic nature of PP can initiate bacterial attachment and subsequent biofilm formation. Herein, we propose a facile approach to functionalize PP non-woven with poly(ethylene glycol) (PEG) and poly(N-vinyl pyrrolidone)-iodine complex (PVP-I). PVP and PEG were successively tethered onto PP non-woven surface via versatile bioinspired dopamine (DA) chemistry, followed by complexing iodine with PVP moieties. It was demonstrated through the field emission scanning electron microscope (SEM) and spread plate method that the as-modified PP non-woven integrated both antifouling property of PEG for suppressing bacterial adhesion, and bactericidal property of PVP-I for killing the few adherent bacteria. Meanwhile, it could greatly resist platelet and red blood cell adhesion. The integrated antifouling and bactericidal PP non-woven surfaces might have great potential in various wound dressing applications.

  13. The Inhibition of Aluminum Corrosion in Sulfuric Acid by Poly(1-vinyl-3-alkyl-imidazolium Hexafluorophosphate

    Directory of Open Access Journals (Sweden)

    Paulina Arellanes-Lozada

    2014-08-01

    Full Text Available Compounds of poly(ionic liquids (PILs, derived from imidazole with different alkylic chain lengths located in the third position of the imidazolium ring (poly(1-vinyl-3-dodecyl-imidazolium (PImC12, poly(1-vinyl-3-octylimidazolium (PImC8 and poly(1-vinyl-3-butylimidazolium (PImC4 hexafluorophosphate were synthesized. These compounds were tested as corrosion inhibitors on aluminum alloy AA6061 in diluted sulfuric acid (0.1–1 M H2SO4 by weight loss tests, polarization resistance measurements and inductively coupled plasma optical emission spectroscopy. Langmuir’s isotherms suggested film formation on bare alloy while standard free energy indicated inhibition by a physisorption process. However, compound efficiencies as inhibitors ranked low (PImC12 > PImC8 > PImC4 to reach 61% for PImC12 in highly diluted acidic solution. Apparently, the high mobility of sulfates favored their adsorption in comparison to PILs. The surface film displayed general corrosion, and pitting occurred as a consequence of PILs’ partial inhibition along with a continuous dissolution of defective patchy film on formation. A slight improvement in efficiency was displayed by compounds having high molecular weight and a long alkyl chain, as a consequence of steric hindrance and PIL interactions.

  14. The Inhibition of Aluminum Corrosion in Sulfuric Acid by Poly(1-vinyl-3-alkyl-imidazolium Hexafluorophosphate).

    Science.gov (United States)

    Arellanes-Lozada, Paulina; Olivares-Xometl, Octavio; Guzmán-Lucero, Diego; Likhanova, Natalya V; Domínguez-Aguilar, Marco A; Lijanova, Irina V; Arce-Estrada, Elsa

    2014-08-07

    Compounds of poly(ionic liquid)s (PILs), derived from imidazole with different alkylic chain lengths located in the third position of the imidazolium ring (poly(1-vinyl-3-dodecyl-imidazolium) (PImC 12 ), poly(1-vinyl-3-octylimidazolium) (PImC₈) and poly(1-vinyl-3-butylimidazolium) (PImC₄) hexafluorophosphate) were synthesized. These compounds were tested as corrosion inhibitors on aluminum alloy AA6061 in diluted sulfuric acid (0.1-1 M H₂SO₄) by weight loss tests, polarization resistance measurements and inductively coupled plasma optical emission spectroscopy. Langmuir's isotherms suggested film formation on bare alloy while standard free energy indicated inhibition by a physisorption process. However, compound efficiencies as inhibitors ranked low (PImC 12 > PImC₈ > PImC₄) to reach 61% for PImC 12 in highly diluted acidic solution. Apparently, the high mobility of sulfates favored their adsorption in comparison to PILs. The surface film displayed general corrosion, and pitting occurred as a consequence of PILs' partial inhibition along with a continuous dissolution of defective patchy film on formation. A slight improvement in efficiency was displayed by compounds having high molecular weight and a long alkyl chain, as a consequence of steric hindrance and PIL interactions.

  15. Investigation on the thermal properties of new thermo-reversible networks based on poly(vinyl furfural and multifunctional maleimide compounds

    Directory of Open Access Journals (Sweden)

    C. Gaina

    2012-02-01

    Full Text Available New thermo-reversible networks were obtained from poly(vinyl furfural and multifunctional maleimide monomers by Diels-Alder (DA and retro-DA reactions. The poly(vinyl furfural having acetalization degree of 15 and 25% were obtained by the acid-catalyzed homogenous acetalization of poly(vinyl alcohol with 2-furfural in a nonaqueous media. The thermal and viscoelastic behaviour of the cross-linked materials have been studied via differential scanning calorimetry, dynamic mechanical analysis and thermogravimetric analysis. The networks exhibit considerable swelling in those organic solvents that dissolve both poly(vinyl furfural and bismaleimides; by heating in aprotic dipolar solvents at 150°C, they become soluble.

  16. Colloidal titration of aqueous zirconium solutions with poly(vinyl sulfate) by potentiometric endpoint detection using a toluidine blue selective electrode.

    Science.gov (United States)

    Sakurada, Osamu; Kato, Yasutake; Kito, Noriyoshi; Kameyama, Keiichi; Hattori, Toshiaki; Hashiba, Minoru

    2004-02-01

    Zirconium oxy-salts were hydrolyzed to form positively charged polymer or cluster species in acidic solutions. The zirconium hydrolyzed polymer was found to react with a negatively charged polyelectrolyte, such as poly(vinyl sulfate), and to form a stoichiometric polyion complex. Thus, colloidal titration with poly(vinyl sulfate) was applied to measure the zirconium concentration in an acidic solution by using a Toluidine Blue selective plasticized poly(vinyl chloride) membrane electrode as a potentiometric end-point detecting device. The determination could be performed with 1% of the relative standard deviation. The colloidal titration stoichiometry at pH < or = 2 was one mol of zirconium per equivalent mol of poly(vinyl sulfate).

  17. Poly(acrylic acid)-block-poly(vinyl alcohol) anchored maghemite nanoparticles designed for multi-stimuli triggered drug release

    Science.gov (United States)

    Liu, Ji; Detrembleur, Christophe; Debuigne, Antoine; de Pauw-Gillet, Marie-Claire; Mornet, Stéphane; Vander Elst, Luce; Laurent, Sophie; Labrugère, Christine; Duguet, Etienne; Jérôme, Christine

    2013-11-01

    Original core/corona nanoparticles composed of a maghemite core and a stimuli-responsive polymer coating made of poly(acrylic acid)-block-poly(vinyl alcohol) macromolecules were fabricated for drug delivery system (DDS) application. This kind of DDS aims to combine the advantage of stimuli-responsive polymer coating, in order to regulate the drug release behaviours under different conditions and furthermore, improve the biocompatibility and in vivo circulation half-time of the maghemite nanoparticles. Drug loading capacity was evaluated with methylene blue (MB), a cationic model drug. The triggered release of MB was studied under various stimuli such as pH, ionic strength and temperature. Local heating generated under alternating magnetic field (AMF) application was studied, and remotely AMF-triggered release was also confirmed, while a mild heating-up of the release medium was observed. Furthermore, their potential application as magnetic resonance imaging (MRI) contrast agents was explored via relaxivity measurements and acquisition of T2-weighted images. Preliminary studies on the cytotoxicity against mouse fibroblast-like L929 cell line and also their cellular uptake within human melanoma MEL-5 cell line were carried out. In conclusion, this kind of stimuli-responsive nanoparticles appears to be promising carriers for delivering drugs to some tumour sites or into cellular compartments with an acidic environment.Original core/corona nanoparticles composed of a maghemite core and a stimuli-responsive polymer coating made of poly(acrylic acid)-block-poly(vinyl alcohol) macromolecules were fabricated for drug delivery system (DDS) application. This kind of DDS aims to combine the advantage of stimuli-responsive polymer coating, in order to regulate the drug release behaviours under different conditions and furthermore, improve the biocompatibility and in vivo circulation half-time of the maghemite nanoparticles. Drug loading capacity was evaluated with methylene

  18. Influence of gamma irradiation on polymerization of pyrrole and glucose oxidase immobilization onto poly (pyrrole)/poly (vinyl alcohol) matrix

    Science.gov (United States)

    Idris, Sarada; A. Bakar, Ahmad Ashrif; Thevy Ratnam, Chantara; Kamaruddin, Nur Hasiba; Shaari, Sahbudin

    2017-04-01

    This paper describes the immobilization of glucose oxidase, GOx onto polymer matrix comprising of poly(pyrrole), PPy and poly(vinyl alcohol), PVA using gamma irradiation technique. Py/PVA-GOx film was prepared by spreading PVA:GOx, 1:1 solution onto dried pyrrole film and exposed to gamma irradiation from cobalt 60 source at doses ranging from 0 to 60 kGy. The films were subjected to structural and morphological analyses by using Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), Scanning electron microscope (SEM), Field emission scanning electron microscope (FESEM) and Atomic-force microscopy (AFM) techniques. Similar studies were also made on pristine pyrrole film which served as control. The SEM and FTIR spectra of Py/PVA-GOx film revealed that pyrrole has been successfully polymerized through irradiation-induced reactions. The results on the morphological properties of the samples characterize using FESEM, SEM and AFM further confirmed the occurrence of radiation-induced modification of Py/PVA-GOx film. The FTIR spectra showed the existence of intermolecular interaction between polymer matrix and GOx indicating that GOx had been successfully immobilized onto Ppy/PVA matrix by radiation-induced reactions. Results revealed that radiation induced reactions such as polymerization of pyrrole, crosslinking of PVA, grafting between the adjacent PVA and pyrrole molecules as well as immobilization of GOx onto Ppy/PVA matrix occurred simultaneously upon gamma irradiation. The optimum dose for GOx immobilization in the polymer matrix found to be 40 kGy. Therefore it is clear that this irradiation technique offered a simple single process to produce Py/PVA-GOx film without additional crosslinking and polymerization agents.

  19. Vitamin C and Poly(ethylene glycol) Protect Concentrated Poly(vinyl alcohol) Solutions against Radiation Cross-linking

    International Nuclear Information System (INIS)

    Oral, E.

    2006-01-01

    There is a need for an injectable material to augment damaged cartilage. We propose to make such self-associating poly(vinyl alcohol) (PVA) hydrogels. Physical associations can be formed in PVA using a gellant such as polyethylene glycol (PEG). The injectability of PVA solutions is compromised when sterilized due to chemical cross-linking. We hypothesized that an anticross-linking agent could prevent cross-linking of irradiated PVA solutions. PVA (17.5 wt/v %, MW= 115,000 g/mol) was prepared in water at 90 degree. PEG (MW=400 g/mol) was added at a ratio of PEG unit to PVA unit of 17, 86, 290, and 639 mol/mol. PVA solutions (17.5 wt/v %, MW= 16,000, 61,000, 81,000 and 115,000 g/mol) were also prepared. Vitamin C was added at a molar ratio of vitamin C to PVA unit of 0.75-10.4. Solutions were poured into syringes and γ-irradiated. The viscosity of injectable solutions was determined by using the bubble tube. Gel content of cross-linked samples was measured by boiling gels in water for 6 hours, drying at 90 degree and calculating the ratio of dry weight to 'as is' weight

  20. Poly(vinyl chloride) catheters modified with pH-responsive poly(methacrylic acid) with affinity for antimicrobial agents

    Science.gov (United States)

    Zuñiga-Zamorano, Ivette; Meléndez-Ortiz, H. Iván; Costoya, Alejandro; Alvarez-Lorenzo, Carmen; Concheiro, Angel; Bucio, Emilio

    2018-01-01

    Radiation-grafting of pH-responsive methacrylic acid (MAA) onto poly(vinyl chloride) (PVC) was carried out by the pre-irradiation method using gamma rays, which demonstrated to be an efficient and fast procedure for obtaining PVC-g-MAA copolymers. The influence of preparation conditions, such as absorbed dose, monomer concentration, reaction time, and reaction temperature on the grafting yield was studied. The grafting of MAA onto PVC catheters was confirmed by means of Fourier transform infrared spectroscopy (FT-IR), thermogravimetry analysis (TGA), and differential scanning calorimetry (DSC). The pH-responsiveness of the grafted copolymers (critical point 8.5) was measured by swelling under cyclic changes in the pH of the medium. Interestingly, PVC-g-MAA showed enhanced capability to immobilize benzalkonium chloride and, particularly, ciprofloxacin and to sustain the release this antimicrobial agent at both acid and alkaline pH. Tests carried out with Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus point out that the developed functionalized catheters may play a role in the prevention/management of urinary tract infections.

  1. Effect of Poly(Vinyl Alcohol) Addition on the Properties of Hydrothermal Derived Calcium Phosphate Cement for Bone Filling Materials

    Science.gov (United States)

    Razali, N. N.; Sopyan, I.; Mel, M.; Salleh, H. M.; Rahman, M. M.; Singh, R.

    2017-06-01

    The effect of addition of poly(vinyl alcohol) on hydrothermal derived calcium phosphate cement has been studied. The precursors used to prepare the cement were calcium oxide (CaO) and ammonium dihydrogen phosphate (NH4H2PO4); the reaction was conducted in water at 80-100°C. To improve properties of CPC, poly(vinyl alcohol) (PVA) of 1wt% and 2wt% was added to the liquid phase of CPC and the results were compared to CPC without PVA addition. The addition of PVA was proved to bring remarkable effects on cohesion, setting time and mechanical strength of CPC which make it suitable physically for injectable bone filler applications.

  2. Effects of Concentration of Organically Modified Nanoclay on Properties of Sulfonated Poly(vinyl alcohol Nanocomposite Membranes

    Directory of Open Access Journals (Sweden)

    Apiradee Sanglimsuwan

    2011-01-01

    Full Text Available Electrolyte nanocomposite membranes for proton exchange membrane fuel cells and direct methanol fuel cells were prepared by carrying out a sulfonation of poly(vinyl alcohol with sulfosuccinic acid and adding a type of organically modified montmorillonite (layered silicate nanoclay commercially known as Cloisite 93A. The effects of the different concentrations (0, 2, 4, 6, 8 wt. % of the organoclay in the membranes on water uptake, ion exchange capacity (IEC, proton conductivity, and methanol permeability were measured, respectively, via gravimetry, titration, impedance analysis, and gas chromatography techniques. The IEC values remained constant for all concentrations. Water uptakes and proton conductivities of the nanocomposite membranes changed with the clay content in a nonlinear fashion. While all the nanocomposite membranes had lower methanol permeability than Nafion115, the 6% concentration of Cloisite 93A in sulfonated poly(vinyl alcohol membrane displayed the greatest proton conductivity to methanol permeability ratio.

  3. In vitro and ex vivo hemocompatibility of off-the-shelf modified poly(vinyl alcohol) vascular grafts

    OpenAIRE

    Cutiongco, Marie Francene A.; Anderson, Deirdre E. J.; Hinds, Monica T.; Yim, Evelyn K. F.

    2015-01-01

    Synthetic small diameter vascular grafts with mechanical properties of native arteries, resistance to thrombosis and capacity to stimulate in situ endothelialization are an unmet clinical need. Poly(vinyl alcohol) hydrogel (PVA) is an excellent candidate as a vascular graft due to its tunable mechanical properties. However, the hydrophilicity and bio-inertness of PVA prevents endothelialization in vivo. We hypothesize that the modification of PVA with biomolecules and topographies creates a h...

  4. A photo-crosslinked poly(vinyl alcohol) hydrogel growth factor release vehicle for wound healing applications

    OpenAIRE

    Bourke, Sharon L.; Al-Khalili, Mohammad; Briggs, Tonye; Michniak, Bozena B.; Kohn, Joachim; Poole-Warren, Laura A.

    2003-01-01

    The objective of this study was to develop and evaluate a hydrogel vehicle for sustained release of growth factors for wound healing applications. Hydrogels were fabricated using ultraviolet photo-crosslinking of acrylamide-functionalized nondegradable poly(vinyl alcohol) (PVA). Protein permeability was initially assessed using trypsin inhibitor (TI), a 21 000 MW model protein drug. TI permeability was altered by changing the solids content of the gel and by adding hydrophilic PVA fillers. As...

  5. Surface grafting of poly(ethylene glycol) onto poly(acrylamide-co-vinyl amine) cross-linked films under mild conditions.

    Science.gov (United States)

    Yamamoto, Y; Sefton, M V

    1998-01-01

    Poly(ethylene glycol) (PEG) was grafted onto poly(acrylamide-co-vinyl amine) (poly(AM-co-VA)) film using tresylated PEG (TPEG) at 37 degrees C in aqueous buffers (pH 7.4) with a view to surface-modifying microencapsulated mammalian cells. Poly(AM-co-VA) film was synthesized by Hofmann degradation of a cross-linked poly(acrylamide) film. Conversion to vinyl amine on the surface of the film was approximately 50%, but bulk conversion was not observed; surface specificity was thought to be the result of cleavage of aminated polymer chains at the surface due to chain scission. Reaction between primary amine and TPEG gave a graft yield of 2 mol% (based on XPS) with respect to available surface amine groups, equivalent to 54 mol% ethylene oxide based on monomer units. Physical adsorption of non-activated polymer was done under identical conditions as a control and the difference in oxygen content was significant compared to TPEG. The type of buffer agent and buffer concentration did not influence graft yields. This graft reaction, which was completed in as little as 2 h was considered to be mild enough to be used for a surface modification of microcapsules containing cells without affecting their viability. Such a surface modification technique may prove to be a useful means of enhancing the biocompatibility of microcapsules (or any tissue engineering construct) even after cell encapsulation or seeding.

  6. Poly(vinyl alcohol)-based film potentially suitable for antimicrobial packaging applications.

    Science.gov (United States)

    Musetti, Alessandro; Paderni, Katia; Fabbri, Paola; Pulvirenti, Andrea; Al-Moghazy, Marwa; Fava, Patrizia

    2014-04-01

    This work aimed at developing a thin and water-resistant food-grade poly(vinyl alcohol) (PVOH)-based matrix able to swell when in contact with high moisture content food products without rupturing to release antimicrobial agents onto the food surface. This film was prepared by blending PVOH and 7.20% (wt/wt of PVOH) of poly(ethylene glycol) (PEG) with citric acid as crosslinking agent. The film-forming solution was then casted onto a flat surface and the obtained film was 60 μm in thickness and showed a good transparency (close to T = 100%) in the visible region (400 to 700 nm). After immersion in water for 72 h at room temperature, the crosslinked matrix loses only 19.2% of its original weight (the percentage includes the amount of unreacted crosslinking agent, antimicrobial in itself). Water content, degree of swelling, and crosslinking density of the film prove that the presence of PEG diminishes the hydrophilic behavior of the material. Also the mechanical properties of the wet and dry film were assessed. Alongside this, 2.5% (wt/wt of dry film) of grapefruit seed extract (GSE), an antimicrobial agent, was added to the film-forming solution just before casting and the ability of the plastic matrix to release the additive was then evaluated in vitro against 2 GSE-susceptible microorganisms, Salmonella enteritidis and Listeria innocua. The results indicate that the developed matrix may be a promising food-grade material for the incorporation of active substances. © 2014 Institute of Food Technologists®

  7. Elastic properties of thin poly(vinyl alcohol)–cellulose nanocrystal membranes

    International Nuclear Information System (INIS)

    Pakzad, A; Yassar, R S; Simonsen, J

    2012-01-01

    In spite of extensive studies on the preparation and characterization of nanocomposite materials, the correlation of their properties at the nanoscale with those in bulk is a relatively unexplored area. This is of great importance, especially for materials with potential biomedical applications, where surface properties are as important in determining their applicability as bulk characteristics. In this study, the nanomechanical characteristics of thin poly(vinyl alcohol) (PVOH)–poly(acrylic acid) (PAA)–cellulose nanocrystal (CNC) membranes were studied using the nanoindentation module in an atomic force microscope (AFM) and the properties were compared with the macro-scale properties obtained by tensile tests. In general, the elastic properties measured by nanoindentation followed the same trend as macro-scale tensile tests except for the PVOH 85-PAA 0-CNC 15 sample. In comparison to the macro-scale elastic properties, the measured elastic moduli with AFM were higher. Macro-scale tensile test results indicated that, in the presence of PAA, incorporation of CNCs up to 20 wt% improved the elastic modulus of PVOH, but when no PAA was added, increasing the CNC content above 10 wt% resulted in their agglomeration and degradation in mechanical properties of PVOH. The discrepancy between macro-scale tensile tests and nanoindentation in the PVOH 85-PAA 0-CNC 15 sample was correlated to the high degree of inhomogeneity of CNC dispersion in the matrix. It was found that the composites reinforced with cellulose nanocrystals had smaller indentation imprints and the pile-up effect increased with the increase of cellulose nanocrystal content. (paper)

  8. Porous poly(vinyl alcohol)/sepiolite bone scaffolds: Preparation, structure and mechanical properties

    International Nuclear Information System (INIS)

    Killeen, Derek; Frydrych, Martin; Chen Biqiong

    2012-01-01

    Porous poly(vinyl alcohol) (PVA)/sepiolite nanocomposite scaffolds containing 0–10 wt.% sepiolite were prepared by freeze-drying and thermally crosslinked with poly(arylic acid). The microstructure of the obtained scaffolds was characterised by scanning electron microscopy and micro-computed tomography, which showed a ribbon and ladder like interconnected structure. The incorporation of sepiolite increased the mean pore size and porosity of the PVA scaffold as well as the degree of anisotropy due to its fibrous structure. The tensile strength, modulus and energy at break of the PVA solid material that constructed the scaffold were found to improve with additions of sepiolite by up to 104%, 331% and 22% for 6 wt.% clay. Such enhancements were attributed to the strong interactions between the PVA and sepiolite, the good dispersion of sepiolite nanofibres in the matrix and the intrinsic properties of the nanofibres. However, the tensile properties of the PVA scaffold deteriorated in the presence of sepiolite because of the higher porosity, pore size and degree of anisotropy. The PVA/sepiolite nanocomposite scaffold containing 6 wt.% sepiolite was characterised by an interconnected structure, a porosity of 89.5% and a mean pore size of 79 μm and exhibited a tensile strength of 0.44 MPa and modulus of 14.9 MPa, which demonstrates potential for this type of materials to be further developed as bone scaffolds. - Highlights: ► Novel PAA-crosslinked PVA/sepiolite nanocomposite scaffolds were prepared. ► They were highly porous with interconnected structures and exhibited good mechanical properties. ► The effects of sepiolite nanofibres on structure and properties of the scaffolds were investigated. ► Sepiolite nanofibres improved the mechanical properties of the solid material significantly.

  9. Self-assembled amphiphilic polyhedral oligosilsesquioxane (POSS) grafted poly(vinyl alcohol) (PVA) nanoparticles

    International Nuclear Information System (INIS)

    Sheikh, Faheem A.; Barakat, Nasser A.M.; Kim, Byoung-Suhk; Aryal, Santosh; Khil, Myung-Seob; Kim, Hak-Yong

    2009-01-01

    In the present study, spherical nanoparticles (NPs) containing polyhedral oligosilsesquioxane (POSS) as an inner hydrophobic core and poly(vinyl alcohol) PVA as a hydrophilic outer shell were prepared by dialysis approach. Preparation of amphiphilic POSS-grafted-PVA co-polymer was characterized by 1 H NMR and FT-IR. The results indicated urethane linkage between monoisocyanate group of POSS macromer and the hydroxyl groups of PVA. The dynamic light scattering (DLS) and electrophoretic light scattering (ELS) of the NPs revealed that they have an average hydrodynamic diameter and negative zeta (ζ)-potential of 215 nm and - 161 mV, respectively. Atomic force microscopy (AFM) and bio-transmission electron microscope (BIO-TEM) have shown unagglomerated NPs within a diameter range of 60-90 nm. The prepared NPs were investigated to improve the control release of anticancer drug; paclitaxel as a model drug. Due to drug loading, the hydrodynamic diameter and negative zeta (ζ)-potential have changed to 325 nm and - 14 mV, respectively. In addition, in-vitro drug release experiments were conducted; the obtained results explicated continuous release for over 40 days. However, in case of using pure drug only, the drug completely released within 1 h.

  10. Mucoadhesive polymers: Synthesis and in vitro characterization of thiolated poly(vinyl alcohol).

    Science.gov (United States)

    Suchaoin, Wongsakorn; Pereira de Sousa, Irene; Netsomboon, Kesinee; Rohrer, Julia; Hoffmann Abad, Patricia; Laffleur, Flavia; Matuszczak, Barbara; Bernkop-Schnürch, Andreas

    2016-04-30

    The aim of this study was to synthesize thiolated poly(vinyl alcohol) (PVA) and to evaluate its mucoadhesive properties. Thiourea and 3-mercaptopropionic acid were utilized in order to obtain thiolated PVAs, namely, TPVA1 and TPVA2, respectively. TPVA1 and TPVA2 displayed 130.44 ± 14.99 and 958.35 ± 155.27 μmol immobilized thiol groups per gram polymer, respectively, which were then evaluated regarding reactivity of thiol groups, swelling behavior and mucoadhesive properties. Both thiolated PVAs exhibited the highest reactivity at pH 8.0 whereas more than 95% of free thiol groups were preserved at pH 5.0. Thiolation of PVA decelerated water uptake and prolonged disintegration time of test discs compared to unmodified PVA. Contact time of TPVA1- and TPVA2-based test discs on porcine intestinal mucosa was 3.2- and 15.8-fold prolonged, respectively, in comparison to non-thiolated PVA as measured by rotating cylinder method. According to tensile studies on mucosa, the total work of adhesion (TWA) and the maximum detachment force (MDF) were increased when compared to PVA. Furthermore, thiolated PVAs preserved higher percentage of viable cells compared to unmodified PVA within 24h as evaluated by MTT assay. Accordingly, thiolated PVA represents a novel excipient that can likely improve the mucoadhesive properties of various pharmaceutical formulations. Copyright © 2016 Elsevier B.V. All rights reserved.

  11. Superstretchable Nacre-Mimetic Graphene/Poly(vinyl alcohol) Composite Film Based on Interfacial Architectural Engineering.

    Science.gov (United States)

    Zhao, Nifang; Yang, Miao; Zhao, Qian; Gao, Weiwei; Xie, Tao; Bai, Hao

    2017-05-23

    Through designing hierarchical structures, particularly optimizing the chemical and architectural interactions at its inorganic/organic interface, nacre has achieved an excellent combination of contradictory mechanical properties such as strength and toughness, which is highly demanded yet difficult to achieve by most synthetic materials. Most techniques applied to develop nacre-mimetic composites have been focused on mimicking the "brick-and-mortar" structure, but the interfacial architectural features, especially the asperities and mineral bridges of "bricks", have been rarely concerned, which are of equal importance for enhancing mechanical properties of nacre. Here, we used a modified bidirectional freezing method followed by uniaxial pressing and chemical reduction to assemble a nacre-mimetic graphene/poly(vinyl alcohol) composite film, with both asperities and bridges introduced in addition to the lamellar layers to mimic the interfacial architectural interactions found in nacre. As such, we have developed a composite film that is not only strong (up to ∼150.9 MPa), but also tough (up to ∼8.50 MJ/m 3 ), and highly stretchable (up to ∼10.44%), difficult to obtain by other methods. This was all achieved by only interfacial architectural engineering within the traditional "brick-and-mortar" structure, without introducing a third component or employing chemical cross-linker as in some other nacre-mimetic systems. More importantly, we believe that the design principles and processing strategies reported here can also be applied to other material systems to develop strong and stretchable materials.

  12. Synthesis, characterization and application of biodegradable crosslinked carboxymethyl chitosan/poly(vinyl alcohol) clay nanocomposites

    Energy Technology Data Exchange (ETDEWEB)

    Sabaa, Magdy W.; Abdallah, Heba M.; Mohamed, Nadia A.; Mohamed, Riham R., E-mail: rihamrashad@hotmal.com

    2015-11-01

    Crosslinked poly(vinyl alcohol) (PVA)/carboxymethyl chitosan (CMCh) nanocomposites were synthesized using terephthaloyl diisothiocyanate crosslinker, in the presence of montmorillonite (MMT), in different ratios of the two matrices. Characterization of nanocomposites was performed using different analyses. Swelling behavior was studied in different buffered solutions. It was found that formation of crosslinked CMCh/PVA hydrogels increased the swellability. Metal ion adsorption has also been investigated. The results indicated that crosslinked CMCh adsorbs various metal ions much more than non crosslinked CMCh. Antimicrobial activity was examined against Gram positive bacteria, against Gram negative bacteria, and also against fungi. Results indicated that most of these nanocomposites exhibited good antimicrobial potency. Degradation study was carried out in Simulated Body Fluid (SBF) for different time periods in order to find out degradation index (Di). Results showed that weight loss of most of the nanocomposites increased as a function of incubation time. - Highlights: • CMCh/PVA nanocomposites have been evaluated for activity against bacteria and fungi. • TEM showed that these hydrogels have size 3–19 nm. • Nanocomposites increased metal ion uptake and showed selectivity for cadmium ions. • Biodegradation increased as a function of incubation time in SBF solution. • Biodegradation increased with increase in CMCh and clay in nanocomposites.

  13. Conductive, tough, hydrophilic poly(vinyl alcohol)/graphene hybrid fibers for wearable supercapacitors

    Science.gov (United States)

    Chen, Shaohua; Ma, Wujun; Xiang, Hengxue; Cheng, Yanhua; Yang, Shengyuan; Weng, Wei; Zhu, Meifang

    2016-07-01

    Graphene fibers based flexible supercapacitors have great potential as wearable power sources for textile electronics. However, their electrochemical performance is limited by the serious stacking of graphene sheets and their hydrophobicity in aqueous electrolytes. Meanwhile, their brittleness is unfavorable for practical application. Incorporation of nanofillers into graphene fibers has been proved effective for enhancing their capacitance, whereas often leading to deteriorated mechanical strength. Herein we demonstrate that the strength, toughness and capacitive performance of graphene-based fibers can be significantly enhanced simultaneously, simply by incorporating hydrophilic poly(vinyl alcohol) (PVA) into a non-liquid-crystalline graphene oxide (GO) dispersion before wet spinning and chemical reduction. The structure and properties of the resulted PVA/graphene hybrid fibers are systematically investigated, and the mechanism behind these enhancements is discussed in detail. The hybrid fiber with a PVA/GO weight ratio of 10/90 possesses a strength of 186 MPa, a toughness of 11.3 J cm-3, and a capacitance of 241 F cm-3 in 1 M H2SO4. A solid-state yarn supercapacitor assembled from these fibers exhibits a device energy of 5.97 mW h cm-3, and features excellent flexibility and bending stability. This device is robust enough to be integrated into textile and thus promising as wearable power supply for smart textiles.

  14. Acoustic Behavior of Subfloor Lightweight Mortars Containing Micronized Poly (Ethylene Vinyl Acetate) (EVA).

    Science.gov (United States)

    Brancher, Luiza R; Nunes, Maria Fernanda de O; Grisa, Ana Maria C; Pagnussat, Daniel T; Zeni, Mára

    2016-01-15

    This paper aims to contribute to acoustical comfort in buildings by presenting a study about the polymer waste micronized poly (ethylene vinyl acetate) (EVA) to be used in mortars for impact sound insulation in subfloor systems. The evaluation method included physical, mechanical and morphological properties of the mortar developed with three distinct thicknesses designs (3, 5, and 7 cm) with replacement percentage of the natural aggregate by 10%, 25%, and 50% EVA. Microscopy analysis showed the surface deposition of cement on EVA, with preservation of polymer porosity. The compressive creep test estimated long-term deformation, where the 10% EVA sample with a 7 cm thick mortar showed the lowest percentage deformation of its height. The impact noise test was performed with 50% EVA samples, reaching an impact sound insulation of 23 dB when the uncovered slab was compared with the 7 cm thick subfloor mortar. Polymer waste addition decreased the mortar compressive strength, and EVA displayed characteristics of an influential material to intensify other features of the composite.

  15. Biodegradable Mulches Based on Poly(vinyl Alcohol, Kenaf Fiber, and Urea

    Directory of Open Access Journals (Sweden)

    Boon Khoon Tan

    2015-07-01

    Full Text Available This paper describes the preparation of poly(vinyl alcohol/kenaf fiber (PVOH/KF composites with entrapped urea. The major FTIR peaks of these composites could be identified. These composites are intended for agricultural applications as biodegradable mulches and could be potential carrier materials for fertilizer. The water solubility, release behavior, chemical properties, and thermal stability of the composites were evaluated. The composites lost 25% of their weight after 7 days in water. In a wet environment, urea was released from the composites through its dissolution in water, and around 57% of the urea was released from the composites in 24 h; Thermagravimetric analysis showed that these composites were stable up 150 C. These composites would be able to withstand rain and protect seedlings from the sun when applied in the field as mulches. For around three to four weeks, these biobased mulches could slowly disintegrate as the PVOH binder was gradually dissolved by moisture, releasing the kenaf fibers to serve as soil fertilizer without leaving any undegradable waste for disposal. Hence, they would not pose any risks to the land or biological systems.

  16. Synthesis and characterization of poly(vinyl alcohol) membranes with quaternary ammonium groups for wound dressing.

    Science.gov (United States)

    Chen, Kuo-Yu; Lin, Yu-Sheng; Yao, Chun-Hsu; Li, Ming-Hsien; Lin, Jui-Che

    2010-01-01

    2-[(acryloyloxy)ethyl]Trimethylammonium chloride (AETMAC) was grafted onto poly(vinyl alcohol) (PVA) using ceric ammonium nitrate (CAN) as a redox initiator. A series of graft co-polymer (PVA-g-PAETMAC) membranes with different contents of AETMAC were prepared with a casting method. The incorporation of AETMAC into PVA chains was confirmed by element analysis and Fourier transform infrared spectroscopy. The effects of grafting on the thermal properties, water take, water vapor transmission rate (WVTR), contact angle, antibacterial activity and cytotoxicity of PVA-g-PAETMAC membranes were investigated. The experiment results showed that PVA-g-PAETMAC membrane has a higher equilibrium swelling ratio, surface hydrophilicity and WVTR than pure PVA membrane. Moreover, the higher the content of AETMAC, the higher were equilibrium swelling ratio, surface hydrophilicity and WVTR. In vitro bacterial adhesion study demonstrated a significantly reduced number of Staphylococcus aureus and Escherichia coli on PVA-g-PAETMAC surfaces when compared to PVA surface. In addition, no significant difference in the in vitro cytotoxicity was observed between PVA and PVA-g-PAETMAC membranes. The presence of quaternary ammonium groups did not reduce L929 cell growth. Therefore, the PVA-g-PAETMAC membranes have the potential for wound-dressing application.

  17. The Preparation of Graphene Reinforced Poly(vinyl alcohol Antibacterial Nanocomposite Thin Film

    Directory of Open Access Journals (Sweden)

    Yuan-Cheng Cao

    2015-01-01

    Full Text Available Methylated melamine grafted polyvinyl benzylchloride (mm-g-PvBCl was prepared which was used as additive in poly(vinyl alcohol (PVA and graphene nanosheets (GNs were used to reinforce the mechanical strength. Using casting method, antimicrobial nanocomposite films were prepared with the polymeric biocide loading lever of 1 wt%, 5 wt%, and 10 wt%. Thermogravimetric analysis (TGA characterization revealed the 2.0 wt% of graphene content in resultant nanocomposites films. XRD showed that the resultant GNs 2 theta was changed from 16.6 degree to 23.3 degree. Using Japanese Industry Standard test methods, the antimicrobial efficiency for the loading lever of 1 wt%, 5 wt%, and 10 wt% was 92.0%, 95.8%, and 97.1%, respectively, against gram negative bacteria E. coli and 92.3%, 99.6%, and 99.7%, respectively, against the gram positive S. aureus. These results indicate the prepared nanocomposite films are the promising materials for the food and drink package applications.

  18. Quaternized poly(vinyl alcohol)/alumina composite polymer membranes for alkaline direct methanol fuel cells

    Science.gov (United States)

    Yang, Chun-Chen; Chiu, Shwu-Jer; Chien, Wen-Chen; Chiu, Sheng-Shin

    The quaternized poly(vinyl alcohol)/alumina (designated as QPVA/Al 2O 3) nanocomposite polymer membrane was prepared by a solution casting method. The characteristic properties of the QPVA/Al 2O 3 nanocomposite polymer membranes were investigated using thermal gravimetric analysis (TGA), scanning electron microscopy (SEM), dynamic mechanical analysis (DMA), micro-Raman spectroscopy, and AC impedance method. Alkaline direct methanol fuel cell (ADMFC) comprised of the QPVA/Al 2O 3 nanocomposite polymer membrane were assembled and examined. Experimental results indicate that the DMFC employing a cheap non-perfluorinated (QPVA/Al 2O 3) nanocomposite polymer membrane shows excellent electrochemical performances. The peak power densities of the DMFC with 4 M KOH + 1 M CH 3OH, 2 M CH 3OH, and 4 M CH 3OH solutions are 28.33, 32.40, and 36.15 mW cm -2, respectively, at room temperature and in ambient air. The QPVA/Al 2O 3 nanocomposite polymer membranes constitute a viable candidate for applications on alkaline DMFC.

  19. Enhanced mechanical and thermal properties of poly (vinyl alcohol)/corn starch blends by nanoclay intercalation.

    Science.gov (United States)

    Tian, Huafeng; Wang, Kai; Liu, Di; Yan, Jiaan; Xiang, Aimin; Rajulu, A Varada

    2017-08-01

    Poly (vinyl alcohol) (PVA)/corn starch blend films with enhanced properties were fabricated by melt processing and montmorillonite (MMT) reinforcing. It was revealed that strong hydrogen bonding occurred between the abundant OH groups of the matrix and polar SiOSi and OH groups of MMT. The highly exfoliated MMT nanolayers were randomly dispersed in the matrix containing MMT lower than 10wt%, whereas the intercalated structure was predominant with MMT content higher than 10wt%. With the increase of MMT, the glass transition temperature as well as equilibrium torque increased. The water sorption decreased and water resistant properties were improved with the incorporation of MMT due to the restricted swelling of the matrix by MMT nanolayers. Significant improvement in strength and flexibility were observed due to the fine dispersion of the MMT layers and the strong interaction between MMT and the matrix. The thermal stability was also improved. The MMT nanolayers could act as the heat and mass transport barriers and retard the thermal decomposition of the composites. Copyright © 2017 Elsevier B.V. All rights reserved.

  20. Poly(vinyl alcohol)-Tannic Acid Hydrogels with Excellent Mechanical Properties and Shape Memory Behaviors.

    Science.gov (United States)

    Chen, Ya-Nan; Peng, Lufang; Liu, Tianqi; Wang, Yaxin; Shi, Shengjie; Wang, Huiliang

    2016-10-12

    Shape memory hydrogels have promising applications in a wide variety of fields. Here we report the facile fabrication of a novel type of shape memory hydrogels physically cross-linked with both stronger and weaker hydrogen bonding (H-bonding). Strong multiple H-bonding formed between poly(vinyl alcohol) (PVA) and tannic acid (TA) leads to their coagulation when they are physically mixed at an elevated temperature and easy gelation at room temperature. The amorphous structure and strong H-bonding endow the PVA-TA hydrogels with excellent mechanical properties, as indicated by their high tensile strengths (up to 2.88 MPa) and high elongations (up to 1100%). The stronger H-bonding between PVA and TA functions as the "permanent" cross-link and the weaker H-bonding between PVA chains as the "temporary" cross-link. The reversible breakage and formation of the weaker H-bonding imparts the PVA-TA hydrogels with excellent temperature-responsive shape memory. Wet and dried hydrogel samples with a deformed or elongated shape can recover to their original shapes when immersed in 60 °C water in a few seconds or at 125 °C in about 2.5 min, respectively.

  1. Quickly Updatable Hologram Images Using Poly(N-vinyl Carbazole (PVCz Photorefractive Polymer Composite

    Directory of Open Access Journals (Sweden)

    Wataru Sakai

    2012-08-01

    Full Text Available Quickly updatable hologram images using photorefractive (PR polymer composite based on poly(N-vinyl carbazole (PVCz is presented. PVCz is one of the pioneer materials of photoconductive polymers. PR polymer composite consists of 44 wt % of PVCz, 35 wt % of 4-azacycloheptylbenzylidene-malonitrile (7-DCST as a nonlinear optical dye, 20 wt % of carbazolylethylpropionate (CzEPA as a photoconductive plasticizer and 1 wt % of 2,4,7-trinitro-9-fluorenone (TNF as a sensitizer. PR composite gives high diffraction efficiency of 68% at E = 45 V μm−1. Response speed of optical diffraction is the key parameter for real-time 3D holographic display. The key parameter for obtaining quickly updatable holographic images is to control the glass transition temperature lower enough to enhance chromophore orientation. Object image of the reflected coin surface recorded with reference beam at 532 nm (green beam in the PR polymer composite is simultaneously reconstructed using a red probe beam at 642 nm. Instead of using a coin object, an object image produced by a computer was displayed on a spatial light modulator (SLM and used for the hologram. The reflected object beam from an SLM was interfered with a reference beam on PR polymer composite to record a hologram and simultaneously reconstructed by a red probe beam.

  2. Adsorption of {alpha}-amylase onto poly(N-vinyl 2-pyrrolidone/itaconic acid) hydrogels

    Energy Technology Data Exchange (ETDEWEB)

    Tuemtuerk, Hayrettin; Caykara, Tuncer; Kantoglu, Oemer; Gueven, Olgun

    1999-05-02

    {alpha}-Amylase enzyme was adsorbed on poly(N-vinyl 2-pyrrolidone/itaconic acid) (P(VP/IA)) hydrogels prepared by irradiating the ternary mixtures of VP/IA/water by {gamma}-rays at ambient temperature. The adsorption capacity of the hydrogels was determined to increase from 2.30 to 3.40 mg {alpha}-amylase/g dry gel with increasing amount of IA in gel system. Kinetic parameters were calculated as 2.51 g/dm{sup 3} for K{sub m} and 1.67x10{sup -3} g/dm{sup 3} min for V{sub max} for free enzyme and in the range of 3.88-5.02 g/dm{sup 3} for K{sub m} and 1.62x10{sup -3}-2.27 x 10{sup -3} g/dm{sup 3} min for V{sub max} depending on the amount of IA in the hydrogel. Enzyme activities were found to increase from 49.9% to 77.4% with increasing amount of IA in the gel system and retained their activities for one month storage. On the other hand, the free enzyme loses its activity completely after 20 days.

  3. Electron beam irradiation and addition of poly(vinyl alcohol) affect gelatin based-films properties

    International Nuclear Information System (INIS)

    Inamura, Patricia Y.; Mastro, Nelida L. del

    2015-01-01

    Gelatin is a mixture of high molecular weight polypeptides, product of denaturation, and partial structural degradation of collagen, and one of the first materials employed as biomaterials. Aqueous solutions of gelatin (10%), glycerin as plasticizer and poly(vinyl alcohol) (PVA) up to 10% were prepared in a water bath at 70 deg C under constant stirring. Films were irradiated with 10 and 20 kGy using an electron beam accelerator, dose rate of 22.4 kGy s -1 , energy 1.407 MeV, at room temperature, in the presence of air. After irradiation, mechanical properties, color measurements, water absorption, moisture and film solubility were analyzed. The films showed an improvement in maximum force to rupture the film with increase of the irradiation dose. The higher the puncture force to rupture the lower the elongation at break. Colorimetric tests showed significant differences between samples, and also differences depending of the applied radiation dose, and analyzed color parameter. In water absorption tests a decrease of absorption percentage was found with the increase of the dose for PVA free and 5% PVA samples. The addition of PVA increased the water absorption for all applied doses. The modifications in gelatin colloids can be appointed to radiation-induced crosslinking. Also, the PVA concentration in the samples influenced the resultant material properties. (author)

  4. Thermal stabilization and plasticization of poly(vinyl chloride) by ester thiols: Update and current status

    International Nuclear Information System (INIS)

    Starnes, William H.; Du, Bin; Kim, Soungkyoo; Zaikov, Vadim G.; Ge, Xianlong; Culyba, Elizabeth K.

    2006-01-01

    Poly(vinyl chloride) (PVC) is one of the most important medical plastics. Recently, however, the safety of flexible PVC containing the common plasticizer, di(2-ethylhexyl) phthalate, has been called into question. Widely used heat stabilizers for PVC that incorporate toxic heavy metals also have fallen into disfavor. In order to address these problems, we have synthesized and tested, as potential replacements, several organic thiols that contain one or more carboxylate ester functions and thus are highly compatible with the polymer. When introduced into PVC at high loading levels (e.g., 30-35 parts by weight), the ester thiols are extremely effective as heat stabilizers and also useful as primary plasticizers. When used at a low loading level (e.g., 3 parts by weight), they still are excellent heat stabilizers for both plasticized and rigid PVC. Importantly, their high potency is achieved in the absence of any costabilizers that incorporate heavy metals. Their syntheses are simple and straightforward, and their odors are not offensive, because their volatilities are low. Described here are some typical results obtained with this new additive technology, which was licensed for commercialization in 2005

  5. Electron beam irradiation and addition of poly(vinyl alcohol) affect gelatin based-films properties

    Energy Technology Data Exchange (ETDEWEB)

    Inamura, Patricia Y.; Mastro, Nelida L. del, E-mail: pinamura@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2015-07-01

    Gelatin is a mixture of high molecular weight polypeptides, product of denaturation, and partial structural degradation of collagen, and one of the first materials employed as biomaterials. Aqueous solutions of gelatin (10%), glycerin as plasticizer and poly(vinyl alcohol) (PVA) up to 10% were prepared in a water bath at 70 deg C under constant stirring. Films were irradiated with 10 and 20 kGy using an electron beam accelerator, dose rate of 22.4 kGy s{sup -1}, energy 1.407 MeV, at room temperature, in the presence of air. After irradiation, mechanical properties, color measurements, water absorption, moisture and film solubility were analyzed. The films showed an improvement in maximum force to rupture the film with increase of the irradiation dose. The higher the puncture force to rupture the lower the elongation at break. Colorimetric tests showed significant differences between samples, and also differences depending of the applied radiation dose, and analyzed color parameter. In water absorption tests a decrease of absorption percentage was found with the increase of the dose for PVA free and 5% PVA samples. The addition of PVA increased the water absorption for all applied doses. The modifications in gelatin colloids can be appointed to radiation-induced crosslinking. Also, the PVA concentration in the samples influenced the resultant material properties. (author)

  6. Evaluation of hemocompatibility and endothelialization of hybrid poly(vinyl alcohol) (PVA)/gelatin polymer films.

    Science.gov (United States)

    Ino, Julia M; Sju, Ervi; Ollivier, Véronique; Yim, Evelyn K F; Letourneur, Didier; Le Visage, Catherine

    2013-11-01

    Engineered grafts are still needed for small diameter blood vessels reconstruction. Ideal materials would prevent thrombosis and intimal hyperplasia by displaying hemocompatibility and mechanical properties close to those of native vessels. In this study, poly(vinyl alcohol) (PVA)/gelatin blends were investigated as a potential vascular support scaffold. We modified a chemically crosslinked PVA hydrogel by incorporation of gelatin to improve endothelial cell attachment with a single-step method. A series of crosslinked PVA/gelatin films with specific ratios set at 100:0, 99:1, 95:5, and 90:10 (w/w) were prepared and their mechanical properties were examined by uniaxial tensile testing. Tubes, obtained from sutured films, were found highly compliant (3.1-4.6%) and exhibited sufficient mechanical strength to sustain hemodynamic strains. PVA-based hydrogels maintained low level of platelet adhesion and low thrombogenic potential. Endothelial cell adhesion and proliferation were drastically improved on PVA/gelatin films with a feed gelatin content as low as 1% (w/w), leading to the formation of a confluent endothelium. Hydrogels with higher gelatin content did not sustain complete endothelialization because of modifications of the film surface, including phase segregation and formation of microdomains. Thus, PVA/gelatin (99:1, w/w) hydrogels appear as promising materials for the design of endothelialized vascular materials with long-term patency. Copyright © 2013 Wiley Periodicals, Inc.

  7. A Review of Natural Fiber Reinforced Poly(Vinyl Alcohol Based Composites: Application and Opportunity

    Directory of Open Access Journals (Sweden)

    Boon Khoon Tan

    2015-11-01

    Full Text Available Natural fibers are fine examples of renewable resources that play an important role in the composites industry, which produces superior strength comparable to synthetic fibers. Poly(vinyl alcohol (PVA composites in particular have attracted enormous interest in view of their satisfactory performance, properties and biodegradability. Their performance in many applications such as consumer, biomedical, and agriculture is well defined and promising. This paper reviews the utilization of natural fibers from macro to nanoscale as reinforcement in PVA composites. An overview on the properties, processing methods, biodegradability, and applications of these composites is presented. The advantages arising from chemical and physical modifications of fibers or composites are discussed in terms of improved properties and performance. In addition, proper arrangement of nanocellulose in composites helps to prevent agglomeration and results in a better dispersion. The limitations and challenges of the composites and future works of these bio-composites are also discussed. This review concludes that PVA composites have potential for use in numerous applications. However, issues on technological feasibility, environmental effectiveness, and economic affordability should be considered.

  8. Preparation and characterization of oriented poly(vinyl alcohol)/carbon nanotube composite nanofibers

    Science.gov (United States)

    Shimizu, Akikazu; Kato, Hayato; Sato, Taiga; Kushida, Masahito

    2017-07-01

    Oriented nanofiber mats blended with carbon nanotubes (CNTs) are expected to be applied as cell seeding scaffolds. Biomaterials that are often used for cell seeding scaffolds generally have low mechanical strength and low electrical conductivity; thus, it has been difficult to apply them to tissues such as heart and nerve. In this study, we prepared oriented poly(vinyl alcohol) (PVA) nanofiber mats blended with various CNT concentrations (up to 10 wt %) by electrospinning using the parallel plate electrodes as collectors with applied voltage. The morphology, mechanical properties, and electrical properties of the prepared oriented nanofiber mats were measured by using various techniques such as scanning electron microscopy (SEM). The tensile strength of the oriented nanofiber mats in the applied voltage direction increased from 2.5 to 9.7 MPa with CNT concentration. Furthermore, the electrical conductivity of the oriented nanofiber mats in the applied voltage direction increased from 0.67 × 10-7 to 4.3 × 10-7 S·m-1. Also, the mechanical strength and electrical conductivity of the oriented nanofiber mats in the applied voltage direction were 3-4 and 2-3 times higher than those in the perpendicular direction, respectively.

  9. Biodegradable starch/poly (vinyl alcohol) film reinforced with titanium dioxide nanoparticles

    Science.gov (United States)

    Hejri, Zahra; Seifkordi, Ali Akbar; Ahmadpour, Ali; Zebarjad, Seyed Mojtaba; Maskooki, Abdolmajid

    2013-10-01

    Biodegradable starch/poly (vinyl alcohol)/nano-titanium dioxide (ST/PVA/nano-TiO2) nanocomposite films were prepared via a solution casting method. Their biodegradability, mechanical properties, and thermal properties were also studied in this paper. A general full factorial experimental approach was used to determine effective parameters on the mechanical properties of the prepared films. ST/PVA/TiO2 nanocomposites were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The results of mechanical analysis show that ST/PVA films with higher contents of PVA have much better mechanical properties. In thermal analysis, it is found that the addition of TiO2 nanoparticles improves the thermal stability of the films. SEM micrographs, taken from the fracture surface of samples, illustrate that the addition of PVA makes the film softer and more flexible. The results of soil burial biodegradation indicate that the biodegradability of ST/PVA/TiO2 films strongly depends on the starch proportion in the film matrix. The degradation rate is increased by the addition of starch in the films.

  10. Thermal, mechanical and dielectric properties of poly(vinyl alcohol)/graphene oxide composites

    Science.gov (United States)

    Rathod, Sunil G.; Bhajantri, R. F.; Ravindrachary, V.; Pujari, P. K.; Sheela, T.; Naik, Jagadish

    2014-04-01

    In this work the composite films of poly(vinyl alcohol) (PVA) doped with functionalized Graphene Oxide (GO) were prepared by solution casting method. The films were characterized using FT-IR, DSC, XRD, mechanical properties and dielectric studies at room temperature. FTIR spectra shows the formation of hydrogen bonds between hydroxyl groups of PVA and the hydroxy groups of GO. The DSC thermograms shows the addition of GO to PVA greatly improves the thermal stability of the composites. XRD patterns shows that the GO exfoliated and uniformly dispersed in PVA matrix. Mechanical properties are significantly improved in PVA/GO composites. The tensile strength increased from 8.2 to 13.7 MPa and the Young's modulus increased from 7.5 to 24.8 MPa for 5 wt% GO doped sample. Dielectric spectroscopy showed a highest dielectric constant for the 5 wt% GO doped PVA films. This work provides a potential design strategy on PVA/GO composite, which would lead to higher-performance, flexible dielectric materials, high charge-storage devices.

  11. Effect of nanocellulose isolation techniques on the formation of reinforced poly(vinyl alcohol nanocomposite films

    Directory of Open Access Journals (Sweden)

    H. Y. Zhan

    2012-10-01

    Full Text Available Three techniques including acid hydrolysis (AH, 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO-mediated oxidation (TMO and ultrasonication (US were introduced to isolate nanocellulose from microcrystalline cellulose, in order to reinforce poly(vinyl alcohol (PVA films. Important differences were noticed in fiber quality of nanocellulose and film properties of PVA nanocomposite films. The TMO treatment was more efficient in nanocellulose isolation with higher aspect ratio, surface charge (–47 mV and yields (37%. While AH treatment resulted in higher crystallinity index (88.1% and better size dispersion. The fracture surface, thermal behavior and mechanical properties of the PVA nanocomposite films were investigated by means of scanning electron microscopy (SEM, differential scanning calorimetry (DSC, thermogravimetric analysis (TGA and tensile testing. The results showed that both the TMO-derived and AH-derived nanocellulose could be dispersed homogeneously in the PVA matrices. AH/PVA films had higher elongation at break (51.59% at 6 wt% nanocellulose loading as compared with TMO/PVA, while TMO/PVA films shown superior tensile modulus and strength with increments of 21.5% and 10.2% at 6wt% nanocellulose loading. The thermal behavior of the PVA nanocomposite films was higher improved with TMO-derived nanofibrils addition.

  12. Production and Characterization of a New Bacterial Cellulose/Poly(Vinyl Alcohol Nanocomposite

    Directory of Open Access Journals (Sweden)

    Miguel Gama

    2013-05-01

    Full Text Available Bacterial cellulose (BC is characterized for its high water holding capacity, high crystallinity, an ultrafine fiber network and high tensile strength. This work demonstrates the production of a new interpenetrated polymer network nanocomposite obtained through the incorporation of poly(vinyl alcohol (PVA on the BC matrix and evaluates the effect of oven drying on the morphological, mechanical and mass transfer properties of the composite membranes. Both the addition of PVA and oven drying induce the appearance of larger pores (circa 1–3 µm in average diameter in dried BC/PVA membranes. Both types of treatments also affect the permeability of the composite, as assessed by the diffusion coefficients of polyethylene glycol (PEG molecules (900, 8,000, 35,000 and 100,000 Da across the membranes. Finally, the Young’s modulus of dry pristine BC decreases following PVA incorporation, resulting in a change from 3.5 GPa to 1 GPa and a five-fold loss in tensile strength.

  13. Viscoelastic, Spectroscopic, and Microscopic Characterization of Novel Bio-Based Plasticized Poly(vinyl chloride Compound

    Directory of Open Access Journals (Sweden)

    Mei Chan Sin

    2014-01-01

    Full Text Available Plasticized poly(vinyl chloride (PVC is one of the most widely consumed commodity plastics. Nevertheless, the commonly used plasticizers, particularly phthalates, are found to be detrimental to the environment and human health. This study aimed to investigate the ability of an alternative greener material, medium-chain-length polyhydroxyalkanoates (mcl-PHA, a kind of biopolyester and its thermally degraded oligoesters, to act as a compatible bioplasticizer for PVC. In this study, mcl-PHA were synthesized by Pseudomonas putida PGA1 in shake flask fermentation using saponified palm kernel oil (SPKO and subsequently moderately thermodegraded to low molecular weight oligoesters (degPHA. SEM, ATR-FTIR, 1H-NMR, and DMA were conducted to study the film morphology, microstructure, miscibility, and viscoelastic properties of the PVC-PHA and PVC/degPHA binary blends. Increased height and sharpness of tan δmax⁡ peak for all binary blends reveal an increase in chain mobility in the PVC matrix and high miscibility within the system. The PVC-PHA miscibility is possibly due to the presence of specific interactions between chlorines of PVC with the C=O group of PHA as evidenced by spectroscopic analyses. Dynamic viscoelastic measurements also showed that mcl-PHA and their oligoesters could reduce the Tg of PVC, imparting elasticity to the PVC compounds and decreasing the stiffness of PVC.

  14. Reinforcement of poly (vinyl alcohol films with alpha-chitin nanowhiskers

    Directory of Open Access Journals (Sweden)

    Hugo Lisboa

    2018-03-01

    Full Text Available Abstract Composites Films were produced using Poly (Vinyl Alcohol as the soft material and reinforced with Chitin Nanowhiskers(NWCH as the rigid material. The present work studies the reinforcing mechanisms of NWCH in PVA films, made through a solvent casting technique and characterized for their calorimetric, swelling and mechanical properties. DSC tests revealed a sharp increase of 45 °C in glass transition temperatures with only 1.5% NWCH, while melting temperature had a small increases suggesting an anti-plasticizing effect. Swelling tests revealed decreasing hygoscopy when NWCH volume fraction increases. Estimates for elastic tensile modulus using a model that predicts the formation of a percolating network were not consistent with the experimental data of tensile tests suggesting that contrary to the reinforcement with cellulose nanowhiskers the percolating network is not primarily responsible for the reinforcement of the films. By adjusting the Halpin-Tsai equations, modified by Nielsen it was found that the mechanical properties were mainly influenced by the packing of the NWCH.

  15. Removal of some basic dyes by poly (Vinyl Alcohol/ acrylic acid)Hydrogel

    International Nuclear Information System (INIS)

    Hegazy, S.A.; Abdel-AAl, S.E.; Abdel-Rehim, H.A.; Khalifa, N.A.; El-Hosseiny, E.M.

    2000-01-01

    A study has made on the preparation and properties of poly (vinyl alcohol/ acrylic acid) hydrogel for the purpose of removal of cationic dyes from aqueous solutions. The effect of dose and monomer concentration on the uptake property of the hydrogel toward dye was studied. The uptake of basic methylene blue-9 dye with PVA/AAc was studied by the batch adsorption technique. The effect of pH on the dye uptake was demonstrated to find out that the suitable pH for maximum uptake occurred at pH 5. It was observed that as the concentration of dye is increased the dye uptake decreased. Furthermore, the uptake of dye by hydrogels increased as the temperature was elevated. The recovery of dye adsorbed is possible by treating the hydrogel with 5% HCl. The results obtained suggested this hydrogel possessed good removal properties towards basic methylene blue-9 dye, and this suggests that such hydrogels could be acceptable for practical uses

  16. Preparation and Properties of Nano-Hydroxyapatite/Gelatin/Poly(vinyl alcohol) Composite Membrane.

    Science.gov (United States)

    Liao, Haotian; Shi, Kun; Peng, Jinrong; Qu, Ying; Liao, Jinfeng; Qian, Zhiyong

    2015-06-01

    In this study, the bone-like composite membrane based on blends of gelatin (Gel), nano-hydroxyapatite (n-HA) and poly(vinyl alcohol) (PVA) was fabricated by solvent casting and evaporation methods. The effect of n-HA content and the ratio of Gel/PVA on the properties of the composite was investigated. The Gel/PVA and n-HA/Gel/PVA composite membranes were characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), water contact angle measurement and scanning electron microscopy (SEM). The mechanical properties of the composites were determined by tensile tests. The as prepared composite membranes exhibited hydrophobility, the water contact angle of composite membrane was 126.6 when its mass ratio of n-HA/Gel/PVA was 10/50/40. The tensile strength of composite membranes was greatly increased due to the introduction of n-HA, and the tensile strength was increased to 74.92 MPa when the mass ratio of n-HA/Gel/PVA was 10/50/40. SEM observation indicated that n-HA was dispersed in the membranes and a sea-island structure was formed in the n-HA/Gel/PVA composite membranes, resulting in a significant increase in tensile strength. The as-prepared n-HA/Gel/PVA composite membranes may be applied in the field of bone tissue engineering.

  17. Acoustic Behavior of Subfloor Lightweight Mortars Containing Micronized Poly (Ethylene Vinyl Acetate (EVA

    Directory of Open Access Journals (Sweden)

    Luiza R. Brancher

    2016-01-01

    Full Text Available This paper aims to contribute to acoustical comfort in buildings by presenting a study about the polymer waste micronized poly (ethylene vinyl acetate (EVA to be used in mortars for impact sound insulation in subfloor systems. The evaluation method included physical, mechanical and morphological properties of the mortar developed with three distinct thicknesses designs (3, 5, and 7 cm with replacement percentage of the natural aggregate by 10%, 25%, and 50% EVA. Microscopy analysis showed the surface deposition of cement on EVA, with preservation of polymer porosity. The compressive creep test estimated long-term deformation, where the 10% EVA sample with a 7 cm thick mortar showed the lowest percentage deformation of its height. The impact noise test was performed with 50% EVA samples, reaching an impact sound insulation of 23 dB when the uncovered slab was compared with the 7 cm thick subfloor mortar. Polymer waste addition decreased the mortar compressive strength, and EVA displayed characteristics of an influential material to intensify other features of the composite.

  18. Superabsorbent hydrogel composite based on copolymer cellulose/poly (vinyl alcohol)/CNT

    Energy Technology Data Exchange (ETDEWEB)

    Khoerunnisa, Fitri, E-mail: fitri.khoerunnisa@gmail.com; Hendrawan,; Sonjaya, Yaya; Putri, Oceu Dwi [Department of Chemistry, Indonesia University of Education, Setiabudi 229 Bandung, West Java, Indonesia 40154 (Indonesia)

    2016-04-19

    Superabsorbent hydrogels are cross-linked hydrophilic polymers that can absorb and retain a large volume of water, saline solution, or physiological fluids. A distinctive superabsorbent hydrogel composite based on cellulose/ poly (vinyl alcohol)/ carbon nanotubes was successfully synthesized via the graft bio-copolymerization in an aqueous medium with glutaraldehide as a crosslinking agent. The effect of carbon nanotubes (CNT) on water absorption capacity and mechanical properties of superabsorbent composite were particularly investigated. The Fourier transform infrared spectra showed the evidence of copolymerization of hydrogel precursors as well as the interaction of CNT filler with the hydrogel matrices, as indicated by the shifting of peak intensity and position of several functional groups (O-H, C-H sp{sup 3}, C=O, C-N, C-O). The modification of hydrogel surface morphology and porosity owing to CNT insertion was also confirmed by scanning electron microscopy images. The CNT insertion improved the mechanical strength of superabsorbent hydrogel composites. Moreover, insertion of CNT into hydrogel matrix remarkably increased the swelling capacity of superabsorbent composites up to 840%. This huge water absorption capacity of hydrogel composites offers promising applications in development of superabsorbent polymers.

  19. pH sensitivity of emeraldine salt polyaniline and poly(vinyl butyral) blend

    International Nuclear Information System (INIS)

    Nguyen, Hoa Duyen; Hoang, Ngoc Vu; Le, Nguyen Ngan; Nguyen, Thi Ngoc Nhien; Doan, Duc Chanh Tin; Dang, Mau Chien; Nguyen, Thi Ha

    2014-01-01

    pH sensitivity of emeraldine salt polyaniline (ES-PANI) and poly(vinyl butyral) (PVB) blend film was investigated. This blend film can be used as a pH sensing element in new-type pH sensors to replace traditional instruments based on fragile glass electrodes for pH measurement of water in aquaculture farming. Structural and optical characteristic of PANI were studied by Fourier transform infrared spectroscopy (FTIR) and ultraviolet visible spectroscopy (UV–vis). Electrical characterization of ES-PANI:PVB blend films versus pH was performed with chemiresistors fabricated by micro-lithography. A ES-PANI:PVB layer was drop-coated on comb-shaped platinum electrodes patterned on SiO 2 /Si substrates. Scanning electron microscope (SEM) and optical microscope were used to investigate morphology of the fabricated platinum electrodes and the coated polymer blend films. I–V measurements of the polymer-coated chemiresistors were performed at very low relative humidity after the polymer films were exposed to pH 1–8. The results showed that logarithm of electrical resistance of the ES-PANI:PVB films increased almost linearly as pH increased from 1 to 8. The initial results showed that the PANI blend-coated chemiresistors can be used as pH sensors for water quality monitoring. (paper)

  20. Using carboxylated nanocrystalline cellulose as an additive in cellulosic paper and poly (vinyl alcohol) fiber paper.

    Science.gov (United States)

    Cha, Ruitao; Wang, Chengyu; Cheng, Shaoling; He, Zhibin; Jiang, Xingyu

    2014-09-22

    Specialty paper (e.g. cigarette paper and battery diaphragm paper) requires extremely high strength properties. The addition of strength agents plays an important role in increasing strength properties of paper. Nanocrystalline cellulose (NCC), or cellulose whiskers, has the potential to enhance the strength properties of paper via improving inter-fibers bonding. This paper was to determine the potential of using carboxylated nanocrystalline cellulose (CNCC) to improve the strength properties of paper made of cellulosic fiber or poly (vinyl alcohol) (PVA) fiber. The results indicated that the addition of CNCC can effectively improve the strength properties. At a CNCC dosage of 0.7%, the tear index and tensile index of the cellulosic paper reached the maximum of 12.8 mN m2/g and 100.7 Nm/g, respectively. More importantly, when increasing the CNCC dosage from 0.1 to 1.0%, the tear index and tensile index of PVA fiber paper were increased by 67.29%, 22.55%, respectively. Copyright © 2014 Elsevier Ltd. All rights reserved.

  1. Preparation and characterization of poly(vinyl alcohol) hydrogel contain metronidazole by irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Baik, Jae; Park, Jong Seok; Jeong, Jin Oh; Jeong, Sung In; Gwon, Hui Jeong; Ahn, Sung Jun; Lim, Youn Mook [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, Jeongeup (Korea, Republic of)

    2016-11-15

    Periodontitis is disease of damaged gum tissue that is not removed the plaque onto teeth. In case that the symptoms of disease get pain worse, it will have to extract tooth because of tumefy or bleeding at gums so treatment of drug was required to periodontitis. In this study, the hydrogel was prepared by including superior viscous, excellent elastic, and biocompatibility of Poly(vinyl alcohol, PVA) and antimicrobial drug of Metronidazole (MD). The 15 wt% PVA was dissolved in deionized water and then prepared PVA solution was irradiated using gamma-ray at 25 kGy (10 kGy hr{sup -1}). In addition, PVA hydrogel was immersed in each 0.1, 0.25 and 0.5 wt% MD solution using stirrer for 24 hr. The result of the gelation, 0.5 wt% MD loaded PVA hydrogel (76%) was lower than PVA hydrogel (88.2%). The swelling ration of 0.5 wt% MD loaded PVA hydrogel (294.8%) was higher than PVA hydrogel (105.2%). The compressive strength and thermal properties of MD loaded PVA hydrogel was gradually lower. The drug release test of 0.5 wt% MD loaded PVA hydrogel (61%) was higher than 0.1 wt% MD loaded PVA hydrogel (12%). Therefore, MD loaded PVA hygrogel may be a promising tool for periodontitis medicine by gamma-ray.

  2. Preparation and characterization of poly(vinyl alcohol) hydrogel contain metronidazole by irradiation

    International Nuclear Information System (INIS)

    Baik, Jae; Park, Jong Seok; Jeong, Jin Oh; Jeong, Sung In; Gwon, Hui Jeong; Ahn, Sung Jun; Lim, Youn Mook

    2016-01-01

    Periodontitis is disease of damaged gum tissue that is not removed the plaque onto teeth. In case that the symptoms of disease get pain worse, it will have to extract tooth because of tumefy or bleeding at gums so treatment of drug was required to periodontitis. In this study, the hydrogel was prepared by including superior viscous, excellent elastic, and biocompatibility of Poly(vinyl alcohol, PVA) and antimicrobial drug of Metronidazole (MD). The 15 wt% PVA was dissolved in deionized water and then prepared PVA solution was irradiated using gamma-ray at 25 kGy (10 kGy hr"-"1). In addition, PVA hydrogel was immersed in each 0.1, 0.25 and 0.5 wt% MD solution using stirrer for 24 hr. The result of the gelation, 0.5 wt% MD loaded PVA hydrogel (76%) was lower than PVA hydrogel (88.2%). The swelling ration of 0.5 wt% MD loaded PVA hydrogel (294.8%) was higher than PVA hydrogel (105.2%). The compressive strength and thermal properties of MD loaded PVA hydrogel was gradually lower. The drug release test of 0.5 wt% MD loaded PVA hydrogel (61%) was higher than 0.1 wt% MD loaded PVA hydrogel (12%). Therefore, MD loaded PVA hygrogel may be a promising tool for periodontitis medicine by gamma-ray

  3. Carboxymethylcellulose acetate butyrate/poly(4-vinyl-N-pentyl pyridinium bromide blends as antimicrobial coatings

    Directory of Open Access Journals (Sweden)

    L. S. Blachechen

    2015-09-01

    Full Text Available Blends of carboxymethyl cellulose acetate butyrate (CMCAB, a cellulose derivative, and poly(4-vinyl-N-pentyl pyridinium bromide (QPVP-C5, an antimicrobial polymer, were prepared by casting method and characterized by means of Fourier transform infrared vibrational spectroscopy (FTIR, scanning electron microscopy (SEM, thermogravimetric analysis (TGA, differential scanning calorimetry (DSC and contact angle measurements. Miscibility between CMCAB and QPVP-C5 was evidenced by DSC measurements of blends, which showed a single thermal event of Tg, and SEM images, which revealed homogenous morphology, regardless the blend composition. Moreover, thermal stability of QPVP-C5 was substantially enhanced, when it was mixed with CMCAB. Upon increasing the QPVP-C5 content in the blend the wettability and antimicrobial activity against Gram-positive bacteria Micrococcus luteus increased, indicating the surface enrichment by pyridinium groups. In fact, blends with 70 wt% QPVP-C5 reduced 5 log and 4 log the colony-forming units of Micrococcus luteus and Escherichia coli, respectively.

  4. Superabsorbent hydrogel composite based on copolymer cellulose/poly (vinyl alcohol)/CNT

    International Nuclear Information System (INIS)

    Khoerunnisa, Fitri; Hendrawan,; Sonjaya, Yaya; Putri, Oceu Dwi

    2016-01-01

    Superabsorbent hydrogels are cross-linked hydrophilic polymers that can absorb and retain a large volume of water, saline solution, or physiological fluids. A distinctive superabsorbent hydrogel composite based on cellulose/ poly (vinyl alcohol)/ carbon nanotubes was successfully synthesized via the graft bio-copolymerization in an aqueous medium with glutaraldehide as a crosslinking agent. The effect of carbon nanotubes (CNT) on water absorption capacity and mechanical properties of superabsorbent composite were particularly investigated. The Fourier transform infrared spectra showed the evidence of copolymerization of hydrogel precursors as well as the interaction of CNT filler with the hydrogel matrices, as indicated by the shifting of peak intensity and position of several functional groups (O-H, C-H sp"3, C=O, C-N, C-O). The modification of hydrogel surface morphology and porosity owing to CNT insertion was also confirmed by scanning electron microscopy images. The CNT insertion improved the mechanical strength of superabsorbent hydrogel composites. Moreover, insertion of CNT into hydrogel matrix remarkably increased the swelling capacity of superabsorbent composites up to 840%. This huge water absorption capacity of hydrogel composites offers promising applications in development of superabsorbent polymers.

  5. Effect of gamma irradiation on biopolymer composite films of poly(vinyl alcohol) and bacterial cellulose

    Energy Technology Data Exchange (ETDEWEB)

    Jipa, Iuliana Mihaela; Stroescu, Marta [University Politehnica of Bucharest, Department of Chemical Engineering, 313 Splaiul Independentei, Polizu 1-3, 060042 Bucharest (Romania); Stoica-Guzun, Anicuta, E-mail: stoica.anicuta@gmail.com [University Politehnica of Bucharest, Department of Chemical Engineering, 313 Splaiul Independentei, Polizu 1-3, 060042 Bucharest (Romania); Dobre, Tanase; Jinga, Sorin [University Politehnica of Bucharest, Department of Chemical Engineering, 313 Splaiul Independentei, Polizu 1-3, 060042 Bucharest (Romania); Zaharescu, Traian [Advanced Research Institute for Electrical Engineering, 313 Splaiul Unirii, 030138 Bucharest (Romania)

    2012-05-01

    Highlights: Black-Right-Pointing-Pointer The paper reports the obtaining of composite materials between PVA and BC. Black-Right-Pointing-Pointer The composite films were {gamma}-irradiated at doses up to 50 kGy. Black-Right-Pointing-Pointer The films have a good resistance, being suitable as food packaging materials. - Abstract: Composite materials containing in different ratios poly(vinyl alcohol) (PVA), bacterial cellulose (BC) and glycerol (G) as plasticizer were obtained and exposed to different {gamma} radiation doses using an irradiator GAMMATOR provided with {sup 137}Cs source. These films successively received up to 50 kGy absorbed doses at a dose rate of 0.4 kGy/h at room temperature. In order to study the chemical and structural changes during {gamma} irradiation, Fourier-transformed infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and UV-Vis spectroscopy were used. Water vapour permeability (WVP), Hunter colour parameters and hardness were also measured for the irradiated samples. Investigation revealed that WVP was not significantly affected by the irradiation. Colour measurements indicated a slight decrease of pure PVA films transparency and it made clear that all samples became more reddish and yellowish after irradiation. The samples hardness was not affected by the irradiation doses used. However, the results showed no drastic structural or chemical changes of the irradiated samples, which prove, in consequence, a good durability. These composite materials could be used as packaging materials for {gamma} irradiated products.

  6. Degradation of poly(vinyl chloride) films by X-rays radiation

    International Nuclear Information System (INIS)

    Sbampato, M.E.; Kawano, Y.

    1984-01-01

    The degradation of pure poly(vinyl chloride) (PVC) films has been studied by X-rays radiation in vacuum. The films are transparent and become yellow with the exposure of radiation and this colour is enhanced with the time of irradiation. The infrared, ultraviolet and visible spectra changed in the irradiated material. The IR spectra show changes in itensities and band shifting, particularly in the region of C-Cl stretching vibrations indicating the occurrence of dehydrochlorination and a change in the conformation of the degraded PVC. The ultraviolet and visible spectra of irradiated films show a strong absorption band at 240 nm and many shoulders which are associated to dyenes, carbonyl and polyenes with few double bonds formed. The shoulder numbers increase in the spectra of samples kept for three months. This effect indicates that with irradiation, HCl is evolved resulting in the formation of polyenyl radicals, which propagate after irradiation. At the same time, should occur the reaction of these radicals with the atmospheric oxygen with formation of C=0 bonds. (Author) [pt

  7. Fluorescence Imaging in Genipin Crosslinked Chitosan–Poly(vinyl pyrrolidone Hydrogels

    Directory of Open Access Journals (Sweden)

    Simon Matcham

    2016-10-01

    Full Text Available Recent research has identified genipin as a promising natural crosslinking agent for biocompatible hydrogels as genipin is significantly less cytotoxic than current synthetic crosslinking agents, such as glutaraldehyde. Conveniently, fluorophores can be produced when genipin crosslinks. In this study, fluorescence intensity measurements of genipin crosslinked chitosan-poly(vinyl pyrrolidone hydrogels have been explored as a dynamic, in situ method for tracing sol-gel transition. These pH-responsive smart materials have a future in medical applications, in particular in tissue engineering and drug delivery, where methods to follow the process in situ and in real-time are crucial for future advancement. Samples were prepared using deionised water, pH 4, and pH 10 solutions, and studied at 24 and 37 °C over a 24 h period. Both temperature and pH have been found to affect sol-gel transition in the hydrogels studied. The transition from acidic (pH 4 to basic (pH 10 solution resulted in reduced fluorescence intensity suggesting that, under more basic conditions, genipin molecules self-polymerise, reducing the number of molecules available for reaction with the amino groups of chitosan. Three-dimensional representations of the fluorescence present in a hydrogel sample have also been produced from the data, enabling the visualisation of variation in fluorescence with time at the surface of the hydrogel.

  8. Physical changes on the radiation and heat induced poly(Vinyl alcohol) fibers

    Energy Technology Data Exchange (ETDEWEB)

    Nho, Young Chang; Park, Kyung Ran; Park, Jong Seok; Lim, Youn Mook; Kang, Phil Hyun [Research Division for Industry and Environment, Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2016-11-15

    Poly(vinyl alcohol) (PVA) has high tensile strength and flexibility as well as oxygen barrier properties. The water, which acts as a plasticizer, reduces the tensile strength of PVA and swells PVA as well. It needs to have high water-resistant depending on its applications, especially for the use as tire cords. The aim of this work was to investigate the effect of the annealing temperature and radiation on the Gel content and tensile strength of PVA fbers. For this purpose, gel fraction and tensile strength were determined and analyzed. Annealing was performed in the temperature range of 120-180℃ for 10 min. PVA fbers were irradiated by using a conventional electron beam irradiation at a radiation dose of 50⁓200 kGy, at a dose of 10 kGy/pass at room temperature (acceleration voltage of 1 MeV). Annealing markedly increased the Gel content and the tensile strength of PVA fbers. However irradiation lowered the Gel content and the tensile strength of PVA fbers because they were degraded easily by radiation.

  9. Poly(vinyl alcohol) hydrogel coatings with tunable surface exposure of hydroxyapatite.

    Science.gov (United States)

    Moreau, David; Villain, Arthur; Ku, David N; Corté, Laurent

    2014-01-01

    Insufficient bone anchoring is a major limitation of artificial substitutes for connective osteoarticular tissues. The use of coatings containing osseoconductive ceramic particles is one of the actively explored strategies to improve osseointegration and strengthen the bone-implant interface for general tissue engineering. Our hypothesis is that hydroxyapatite (HA) particles can be coated robustly on specific assemblies of PVA hydrogel fibers for the potential anchoring of ligament replacements. A simple dip-coating method is described to produce composite coatings made of microscopic hydroxyapatite (HA) particles dispersed in a poly(vinyl alcohol) (PVA) matrix. The materials are compatible with the requirements for implant Good Manufacturing Practices. They are applied to coat bundles of PVA hydrogel fibers used for the development of ligament implants. By means of optical and electronic microscopy, we show that the coating thickness and surface state can be adjusted by varying the composition of the dipping solution. Quantitative analysis based on backscattered electron microscopy show that the exposure of HA at the coating surface can be tuned from 0 to over 55% by decreasing the weight ratio of PVA over HA from 0.4 to 0.1. Abrasion experiments simulating bone-implant contact illustrate how the coating cohesion and wear resistance increase by increasing the content of PVA relative to HA. Using pullout experiments, we find that these coatings adhere well to the fiber bundles and detach by propagation of a crack inside the coating. These results provide a guide to select coated implants for anchoring artificial ligaments.

  10. Constitutive Investigation on Viscoelasticity of PolyVinyl Butyral: Experiments Based on Dynamic Mechanical Analysis Method

    Directory of Open Access Journals (Sweden)

    Bohan Liu

    2014-01-01

    Full Text Available PolyVinyl Butyral (PVB film is now widely used in automotive industry and architectures serving as the protective interlayer. The dynamic modulus of PVB is measured through systematic experiments based on Dynamic Mechanical Analysis (DMA method at various temperatures, heating rates, and vibration frequencies. Further, viscoelasticity of PVB influenced by time and temperature is systematically studied. Fitted empirical formulas describing the relationship between glass transition temperature and frequency, as well as the heating rate of PVB, are established. The master curve of PVB at 293 K is suggested based on the experiment data as to express the dynamic modulus variation at various frequencies in a wider range. Constitutive behavior of PVB is then analyzed based on Generalized Maxwell (GM model and Fractional Derivative (FD model, respectively. It is shown that PVB has higher efficiency of energy dissipation in its high energy absorption state, while both fifth-order GM model and FD model can characterize the viscoelasticity of PVB at glassy transition area. Results may offer useful fundamental experimental data and important constitutive characteristics of PVB and shed lights on further studies on viscoelasticity behavior of PVB and energy mitigation ability of laminated glass.

  11. Short Oligonucleotides Aligned in Stretched Humid Matrix: Secondary DNA Structure in Poly(vinyl alcohol) Environment

    KAUST Repository

    Hanczyc, Piotr

    2012-04-24

    We report that short, synthetic, double- as well as single-stranded DNA can be aligned in stretched humid poly(vinyl alcohol) (PVA) matrix, and the secondary structure (nucleobase orientation) can be characterized with linear dichroism (LD) spectroscopy. Oligonucleotides of lengths varying between 10 (3.4 nm) and 60 bases (20.4 nm) were investigated with respect to structural properties in the gel-like polymer environment. The DNA conformation as a function of relative humidity reveals a strong dependence of helical structure of DNA on PVA hydration level, results of relevance for nanotechnical studies of DNA-based supramolecular systems. Also, the PVA gel could provide possibilities to test models for nucleic acid interactions and distribution in cell contexts, including structural stability of genetic material in the cell and PVA-packaging for gene delivery. A method by which duplex oligonucleotides, with sequences designed to provide specific binding sites, become amenable to polarized-light spectroscopy opens up new possibilities for studying structure in DNA complexes with small adduct molecules as well as proteins. © 2012 American Chemical Society.

  12. Preparation and properties of Starch-g-PLA/poly(vinyl alcohol) composite film.

    Science.gov (United States)

    Hu, Yingmo; Wang, Qingling; Tang, Mingru

    2013-07-25

    Starch/lactic acid graft copolymer (Starch-g-PLA) was prepared by the in situ copolymerization of starch grafted with lactic acid catalyzed with sodium hydroxide, and then mixed with poly(vinyl alcohol) (PVA) to get composite films. The structures of the graft copolymer and composite films were characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The mechanical properties, water resistance, and thermal stability were also investigated. It was found that the compatibility of Starch-g-PLA and PVA was better than that of starch and PVA in the composite films. The tensile strength and elongation at break of the Starch-g-PLA/PVA composite film increased by 69.15% and 84.22%, respectively, while the water absorption decreased by 50.39%, which overcame the shortcomings of hydrophilicity and poor mechanical properties of Starch/PVA film. Thermogravimetric analysis (TGA) also showed that the thermal stability of Starch-g-PLA/PVA film was improved compared with Starch/PVA film. Copyright © 2013 Elsevier Ltd. All rights reserved.

  13. Fabrication of antibacterial blend film from poly (vinyl alcohol) and quaternized chitosan for packaging

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Dongying; Wang, Lijuan, E-mail: donglinwlj@163.com

    2016-06-15

    Highlights: • HTCC/PVA blend films were prepared through a simple mixing method. • The blend films had greater elongation at break and good optical transmittance. • The blend films had low oxygen permeability and water vapor permeability. • The films had good activity against Escherichia coli and Staphylococcus aureus. - Abstract: Blend films from poly (vinyl alcohol) (PVA) containing N-(2-hydroxy) propyl-3-trimethyl ammonium chloride chitosan (HTCC) were prepared via a simple mixing and casting method. The films were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction measurements (XRD), scanning electron microscopy and ultraviolet-visible measurements (UV–vis). The effects of HTCC amount on mechanical properties, oxygen permeability, water vapor permeation, and antibacterial properties against Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) of the films were investigated. FTIR and XRD analysis show that HTCC and PVA in the blend films interacted by hydrogen bonding. SEM and UV–vis analysis reveal the good compatibility between HTCC and PVA. Compared with pure PVA film, the blend films had greater elongation at break, lower water permeability, and higher antibacterial activity. The HTCC addition decreased the tensile strength and the light transmittance. The results suggest that HTCC/PVA blend films have a potential as packaging materials.

  14. A poly(vinyl alcohol)/sodium alginate blend monolith with nanoscale porous structure.

    Science.gov (United States)

    Sun, Xiaoxia; Uyama, Hiroshi

    2013-10-04

    A stimuli-responsive poly(vinyl alcohol) (PVA)/sodium alginate (SA) blend monolith with nanoscale porous (mesoporous) structure is successfully fabricated by thermally impacted non-solvent induced phase separation (TINIPS) method. The PVA/SA blend monolith with different SA contents is conveniently fabricated in an aqueous methanol without any templates. The solvent suitable for the fabrication of the present blend monolith by TINIPS is different with that of the PVA monolith. The nanostructural control of the blend monolith is readily achieved by optimizing the fabrication conditions. Brunauer Emmett Teller measurement shows that the obtained blend monolith has a large surface area. Pore size distribution plot for the blend monolith obtained by the non-local density functional theory method reveals the existence of the nanoscale porous structure. Fourier transform infrared analysis reveals the strong interactions between PVA and SA. The pH-responsive property of the blend monolith is investigated on the basis of swelling ratio in different pH solutions. The present blend monolith of biocompatible and biodegradable PVA and SA with nanoscale porous structure has large potential for applications in biomedical and environmental fields.

  15. Fabrication of antibacterial blend film from poly (vinyl alcohol) and quaternized chitosan for packaging

    International Nuclear Information System (INIS)

    Hu, Dongying; Wang, Lijuan

    2016-01-01

    Highlights: • HTCC/PVA blend films were prepared through a simple mixing method. • The blend films had greater elongation at break and good optical transmittance. • The blend films had low oxygen permeability and water vapor permeability. • The films had good activity against Escherichia coli and Staphylococcus aureus. - Abstract: Blend films from poly (vinyl alcohol) (PVA) containing N-(2-hydroxy) propyl-3-trimethyl ammonium chloride chitosan (HTCC) were prepared via a simple mixing and casting method. The films were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction measurements (XRD), scanning electron microscopy and ultraviolet-visible measurements (UV–vis). The effects of HTCC amount on mechanical properties, oxygen permeability, water vapor permeation, and antibacterial properties against Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) of the films were investigated. FTIR and XRD analysis show that HTCC and PVA in the blend films interacted by hydrogen bonding. SEM and UV–vis analysis reveal the good compatibility between HTCC and PVA. Compared with pure PVA film, the blend films had greater elongation at break, lower water permeability, and higher antibacterial activity. The HTCC addition decreased the tensile strength and the light transmittance. The results suggest that HTCC/PVA blend films have a potential as packaging materials.

  16. Tailoring of poly(vinyl alcohol cryogels properties by salts addition

    Directory of Open Access Journals (Sweden)

    2009-05-01

    Full Text Available The present paper aims to study the possibility to modify the properties of poly(vinyl alcohol (PVA hydrogels prepared in the presence of different salt types (Na2SO4, NaCl and NaNO3 in order to extend the nature of the salts already used in obtaining films or gels, to expand their concentration domains and to explain the increase of film strain, concomitantly with the increase of their crystallinity. The morphology of the PVA based hydrogels has been studied by Scanning Electronic Microscopy (SEM, the interaction between the PVA macromolecular chains and salts has been determined by Fourier Transform Infrared Spectroscopy (FTIR, while the mechanical properties of the cryogels have been investigated by oscillatory dynamic mechanical measurements. The gels swelling in water have been monitored by gravimetric method in order to evidence the alteration of the PVA cryogel properties such as crystallinity and porosity determined by the salt addition to the initial PVA aqueous solution. The data reported show that the ions present in the PVA solution influence the interaction between PVA-water and PVA-PVA chains; their influence on the salt-based PVA hydrogels follow the Hofmeister lyotropic series.

  17. Post irradiation effects on the graft of poly(tetrafluoroethylene-co-perfluoropropyl vinyl ether) (PFA) films

    International Nuclear Information System (INIS)

    Geraldes, Adriana N.; Zen, Heloisa A.; Ribeiro, Geise; Ferreira, Henrique P.; Souza, Camila P.; Parra, Duclerc F.; Lugao, Ademar B.

    2009-01-01

    Radiation induced grafting of monomers into fluorinated polymers was designed as an alternative route to polymer modification. In this work, grafting of styrene onto poly(tetrafluoroethylene-co-perfluoropropyl vinyl ether) (PFA) was studied. Radiation-induced grafting of styrene onto PFA films was investigated after simultaneous irradiation (in post-irradiation condition) using a 60 Co source. The films of PFA were irradiated at 20, 40, 80 and 100 kGy doses at room temperature and chemical changes were monitored after contact with styrene for grafting. The post-irradiation time was established between 7 and 28 days when films of PFA were maintained in styrene/toluene 1:1 v/v solution at room temperature. After these periods the grafting degrees were evaluated in the samples. The highest degree of grafting was achieved after 14 days. Chemical modifications were evaluated by infrared spectroscopic analysis (FTIR), thermogravimetry (TG), differential scanning calorimetry (DSC) and also by scanning electron microscopy (SEM). The degree of grafting (DOG) was determined gravimetrically. The results showed that irradiated PFA films at 100 kGy exhibited higher grafting degree. Surface analysis by SEM technique of irradiated, grafted and original films have presented an homogeneous surface. (author)

  18. Influence of gamma irradiation on polymerization of pyrrole and glucose oxidase immobilization onto poly (pyrrole)/poly (vinyl alcohol) matrix

    Energy Technology Data Exchange (ETDEWEB)

    Idris, Sarada, E-mail: sarada@nuclearmalaysia.gov.my [Department of Radiation Technology, Malaysian Nuclear Agency, 43000, Bangi, Selangor (Malaysia); Department of Electrical, Electronic and Systems Engineering, Faculty of Engineering & Built Environment, Universiti Kebangsaan Malaysia, Bangi, 43600 (Malaysia); Bakar, Ahmad Ashrif A., E-mail: ashrif@ukm.edu.my [Department of Electrical, Electronic and Systems Engineering, Faculty of Engineering & Built Environment, Universiti Kebangsaan Malaysia, Bangi, 43600 (Malaysia); Thevy Ratnam, Chantara [Department of Radiation Technology, Malaysian Nuclear Agency, 43000, Bangi, Selangor (Malaysia); Kamaruddin, Nur Hasiba [Department of Electrical, Electronic and Systems Engineering, Faculty of Engineering & Built Environment, Universiti Kebangsaan Malaysia, Bangi, 43600 (Malaysia); Shaari, Sahbudin [Institute of Microengineering and Nanoelectronics, Universiti Kebangsaan Malaysia, Bangi, 43600 (Malaysia)

    2017-04-01

    Graphical abstract: The illustration of pyrrole polymerization, PVA crosslinking and immobilization of GOx onto polymer matrix. - Highlights: • Immobilization of glucose oxidase onto polymer matrices by gamma irradiation is proposed. • Crosslinking and grafting of polymers implies the immobilization reaction. • The mechanisms relies on gamma irradiation doses. • A simple single step process of polymerization, cross linking and immobilization by mean of gamma irradiation as was shown in Graphical abstract. - Abstract: This paper describes the immobilization of glucose oxidase, GOx onto polymer matrix comprising of poly(pyrrole), PPy and poly(vinyl alcohol), PVA using gamma irradiation technique. Py/PVA-GOx film was prepared by spreading PVA:GOx, 1:1 solution onto dried pyrrole film and exposed to gamma irradiation from cobalt 60 source at doses ranging from 0 to 60 kGy. The films were subjected to structural and morphological analyses by using Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), Scanning electron microscope (SEM), Field emission scanning electron microscope (FESEM) and Atomic-force microscopy (AFM) techniques. Similar studies were also made on pristine pyrrole film which served as control. The SEM and FTIR spectra of Py/PVA-GOx film revealed that pyrrole has been successfully polymerized through irradiation-induced reactions. The results on the morphological properties of the samples characterize using FESEM, SEM and AFM further confirmed the occurrence of radiation-induced modification of Py/PVA-GOx film. The FTIR spectra showed the existence of intermolecular interaction between polymer matrix and GOx indicating that GOx had been successfully immobilized onto Ppy/PVA matrix by radiation-induced reactions. Results revealed that radiation induced reactions such as polymerization of pyrrole, crosslinking of PVA, grafting between the adjacent PVA and pyrrole molecules as well as immobilization of GOx onto Ppy

  19. Influence of gamma irradiation on polymerization of pyrrole and glucose oxidase immobilization onto poly (pyrrole)/poly (vinyl alcohol) matrix

    International Nuclear Information System (INIS)

    Idris, Sarada; Bakar, Ahmad Ashrif A.; Thevy Ratnam, Chantara; Kamaruddin, Nur Hasiba; Shaari, Sahbudin

    2017-01-01

    Graphical abstract: The illustration of pyrrole polymerization, PVA crosslinking and immobilization of GOx onto polymer matrix. - Highlights: • Immobilization of glucose oxidase onto polymer matrices by gamma irradiation is proposed. • Crosslinking and grafting of polymers implies the immobilization reaction. • The mechanisms relies on gamma irradiation doses. • A simple single step process of polymerization, cross linking and immobilization by mean of gamma irradiation as was shown in Graphical abstract. - Abstract: This paper describes the immobilization of glucose oxidase, GOx onto polymer matrix comprising of poly(pyrrole), PPy and poly(vinyl alcohol), PVA using gamma irradiation technique. Py/PVA-GOx film was prepared by spreading PVA:GOx, 1:1 solution onto dried pyrrole film and exposed to gamma irradiation from cobalt 60 source at doses ranging from 0 to 60 kGy. The films were subjected to structural and morphological analyses by using Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), Scanning electron microscope (SEM), Field emission scanning electron microscope (FESEM) and Atomic-force microscopy (AFM) techniques. Similar studies were also made on pristine pyrrole film which served as control. The SEM and FTIR spectra of Py/PVA-GOx film revealed that pyrrole has been successfully polymerized through irradiation-induced reactions. The results on the morphological properties of the samples characterize using FESEM, SEM and AFM further confirmed the occurrence of radiation-induced modification of Py/PVA-GOx film. The FTIR spectra showed the existence of intermolecular interaction between polymer matrix and GOx indicating that GOx had been successfully immobilized onto Ppy/PVA matrix by radiation-induced reactions. Results revealed that radiation induced reactions such as polymerization of pyrrole, crosslinking of PVA, grafting between the adjacent PVA and pyrrole molecules as well as immobilization of GOx onto Ppy

  20. DC conduction mechanism and dielectric properties of Poly (methyl methacrylate)/Poly (vinyl acetate) blends doped and undoped with malachite green

    International Nuclear Information System (INIS)

    Abd-El Kader, F.H.; Osman, W.H.; Hafez, R.S.

    2013-01-01

    Cast thin films of Poly (methyl methacrylate)/Poly (vinyl acetate) blends of different concentrations undoped and doped with malachite green have been prepared and subjected to both dc electrical conduction and dielectric spectroscopy measurements. The analysis of dc electrical conduction data showed that the space charge limited current mechanism has been dominant for Poly (vinyl acetate) while Schottky-Richardson conduction mechanism prevailed for the Poly (methyl methacrylate) and blended samples. The values of field lowering constant β and the thermal activation energy ΔE involved in the dc conduction were reported, which provide another support for the suggested Schottky-Richardson mechanism. The increase in current for the blend sample doped with malachite green has been attributed to the formation of charge transfer complexes inside the polyblend matrix. The dielectric constant as a function of temperature for all samples have been calculated which are affected by the composition ratio and the addition of dye. The relaxation peak that appeared in the dielectric loss curve at 347 K for the doped blend sample is related to local dipoles that are present in the dye material. The obtained relaxation process spectra present in the investigated samples were analyzed with the well-known model of Havriliak-Negami.

  1. Polymer and Water Dynamics in Poly(vinyl alcohol/Poly(methacrylate Networks. A Molecular Dynamics Simulation and Incoherent Neutron Scattering Investigation

    Directory of Open Access Journals (Sweden)

    Ester Chiessi

    2011-10-01

    Full Text Available Chemically cross-linked polymer networks of poly(vinyl alcohol/poly(methacrylate form monolitic hydrogels and microgels suitable for biomedical applications, such as in situ tissue replacement and drug delivery. In this work, molecular dynamics (MD simulation and incoherent neutron scattering methods are used to study the local polymer dynamics and the polymer induced modification of water properties in poly(vinyl alcohol/poly(methacrylate hydrogels. This information is particularly relevant when the diffusion of metabolites and drugs is a requirement for the polymer microgel functionality. MD simulations of an atomic detailed model of the junction domain at the experimental hydration degree were carried out at 283, 293 and 313 K. The polymer-water interaction, the polymer connectivity and the water dynamics were investigated as a function of temperature. Simulation results are compared with findings of elastic and quasi-elastic incoherent neutron scattering measurements, experimental approaches which sample the same space-time window of MD simulations. This combined analysis shows a supercooled water component and an increase of hydrophilicity and mobility with temperature of these amphiphilic polymer networks.

  2. Poly(vinyl acetate-Based Block Copolymer/Clay Nanocomposites Prepared by In Situ Atom Transfer Radical Polymerization

    Directory of Open Access Journals (Sweden)

    M.A. Semsarzadeh

    2009-12-01

    Full Text Available Atom transfer radical polymerization of styrene (St and methyl methacrylate (MMA was performed at 90oC in the absence and presence of nanoclay (Cloisite 30B. Trichloromethyl-terminated poly(vinyl acetate telomerand CuCl/ PMDETA were used as a macroinitiator and catalyst system, respectively. The experimental results showed that the atom transfer radical polymerization of St and MMA in the absence or presence of nanoclay proceeds via a controlled/living mode. It was observed that nanoclay significantly enhances the homopolymerization rate of MMA, which was attributed to the activated conjugated C=C bond of MMA monomer via interaction between the carbonyl group of MMA monomer and the hydroxyl moiety (Al-O-H of nanoclay as well as the effect of nanoclay on the dynamic equilibrium between the active (macro radicals and dormant species.Homopolymerization rate of St (a non-coordinative monomer with nanoclay decreased slightly in the presence of nanoclay. This could be explained by insertion of a portion of macroinitiator into the clay galleries, where no sufficient St monomer exists due to the low compatibility or interaction of St monomer with nanoclay to react with the macroinitiator. The results obtained from XRD, TEM and TGA analyses were fully in agreement with the kinetic data. Structure of the poly(vinyl acetate-bpolystyrene nanocomposite was found to be a combination of stacking layers and exfoliated structures while poly(vinyl acetate-b-poly(methyl methacryale nanocomposite had an exfoliated structure. This difference in the structure of nanocomposites was attributed to the different capability of the monomers (styrene and methyl methacrylate to react with the hydroxyl moiety (Al-O-H of nanoclay.

  3. Development of new materials by utilizing radiation crosslinking

    International Nuclear Information System (INIS)

    Ueno, Keiji; Uda, Yujiro; Suzuki, Shizuo

    1989-01-01

    About 30 years have elapsed since the cables by electron beam crosslinking were developed as the first industrial utilization of radiation in Japan. At present about 200 electron beam accelerators are used industrially in Japan, and cable industry ranks at the top, followed by foaming polyethylene and curing, and the preliminary vulcanization of tires. The effect of these irradiations is the reforming of polymers by radiation crosslinking. In cables, the heat resistance and chemical resistance of insulators are improved by radiation crosslinking. By applying radiation crosslinking to polyurethane elastomer, its weakest point, waterproof property, was improved. Moreover, by using this crosslinked polyurethane elastomer for cable coating, the reliability of the sensor cables for brake system was able to be remarkably improved. As another new application of radiation crosslinking process, the improvement of the heat resistance of engineering plasties was examined. The structure of radiation crosslinked urethane elastomer cables, their endurance in hot water and oil, and the life, and the characteristics of sensor cables are reported. Multi-functional monomers, the molecular structure, and the various characteristics of engineering plastics are described. (K.I.)

  4. [Preparation and physicochemical property of carboxymethyl-chitosan/hyaluronic acid poly(vinyl alcohol) blend membrane].

    Science.gov (United States)

    Liu, Wen; Li, Shuning; Chang, Jing; Han, Baoqin; Liu, Wanshun

    2009-08-01

    To prepare carboxymethyl-chitosan/hyaluronic acid/poly(vinyl alcohol) (CHP) blend membrane, evaluate its physicochemical properties and intraocular biocompatibility and to investigate its feasibility to be applied to glaucoma filtering surgery. CHP blend membrane was prepared using solution casting method after blending carboxymethyl-chitosan, HA and poly(vinyl alcohol) in a proportion of 5 : 4 : 1 (M/M). Its water absorption rate, swelling rate, permeability, and mechanical properties were detected. Subconjunctival fibroblasts separated from subconjunctival tissue of New Zealand white rabbits were cultured, and the cells at passage 4 were cultured on cell culture plate with or without the CHP blend membrane, serving as the experimental group and the control group, respectively. Effect of the CHP blend membrane on the subconjunctival fibroblasts was tested by MTT method 24, 48, and 72 hours after culture. Six New Zealand white rabbits were randomly divided into two groups (n = 3 rabbits per group), and the CHP blend membrane and SK gel were implanted into the rabbits' subconjunctival space and anterior chamber in the experimental group and the control group, respectively. Slit lamp observation and binocular reaction record were conducted 1, 3, 5, 9, 11, 20, 30, 45, and 60 days after operation. Corneal tissue harvested from the experimental group was observed using scanning electron microscope 15 days after operation to study ophthalmic biocompatibility and biodegradability. The water absorption rate and the swelling rate of the CHP blend membrane was 83.8% +/- 1.3% and 3.59 +/- 0.50, respectively. The tensile strength of the dry and the wet CHP blend membrane was (20.59 +/- 1.73) and (0.51 +/- 0.13) MPa, respectively. The breaking elongation rate of the dry and the wet CHP blend membrane was 10.69% +/- 1.16% and 53.15% +/- 2.46%, respectively. The CHP blend membrane had good permeability to NaCl and L-tyrosine. Absorbance (A) value of the experimental group 24, 48

  5. A facile method for electrospinning of Ag nanoparticles/poly (vinyl alcohol)/carboxymethyl-chitosan nanofibers

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Yinghui; Zhou, Ying [Beijing Key Laboratory for Solid Waste Utilization and Management, College of Engineering, Peking University, Beijing 100871 (China); Center for Biomedical Materials and Tissue Engineering, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871 (China); Wu, Xiaomian [Center for Biomedical Materials and Tissue Engineering, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871 (China); Department of Orthodontics College of Stomatology, Chongqing Medical University, Chongqing 401147 (China); Wang, Lu [Beijing Key Laboratory for Solid Waste Utilization and Management, College of Engineering, Peking University, Beijing 100871 (China); Xu, Ling, E-mail: lingxu@pku.edu.cn [Beijing Key Laboratory for Solid Waste Utilization and Management, College of Engineering, Peking University, Beijing 100871 (China); Center for Biomedical Materials and Tissue Engineering, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871 (China); PKU-HKUST ShenZhen-HongKong Institution, Shenzhen 518057 (China); Wei, Shicheng, E-mail: sc-wei@pku.edu.cn [Center for Biomedical Materials and Tissue Engineering, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871 (China); Department of Oral and Maxillofacial Surgery, School and Hospital of Stomatology, Peking University, Beijing 100081 (China)

    2012-09-01

    Highlights: Black-Right-Pointing-Pointer AgNPs/PVA/CM-chitosan nanofibers were prepared via electrospinning method. Black-Right-Pointing-Pointer AgNPs were in situ synthesized in electrospinning solution via a facile method. Black-Right-Pointing-Pointer AgNPs distributed homogeneously on the surface of nanofibers. Black-Right-Pointing-Pointer The prepared nanofibers possessed certain antibacterial ability against Escherichia coli. Black-Right-Pointing-Pointer The AgNPs containing nanofibers had potential as antibacterial biomaterial. - Abstract: A facile method to prepare silver nanoparticles (AgNPs) containing nanofibers via electrospinning has been demonstrated. AgNPs were in situ synthesized in poly (vinyl alcohol) (PVA)/carboxymethyl-chitosan (CM-chitosan) blend aqueous solution before electrospinning. UV-vis spectra, viscosity and conductivity of the electrospinning solution were measured to investigate their effects on the electrospinning procedure. The morphology of AgNPs/PVA/CM-chitosan nanofibers was observed by Field Emission Scanning Electron Microscopy. The formation and morphology of AgNPs were investigated by Transmission Electron Microscopy and X-ray Photoelectron Spectroscopy. The resulted nanofibers have smooth surface and uniform diameters ranging from 295 to 343 nm. The diameters of AgNPs mainly distributed in the range of 4-14 nm, and the electrostatic interaction between AgNPs and fibers was observed. Finally, in vitro Ag release from the nanofibers was measured and the antibacterial behavior of the nanofibers against Escherichia coli was studied by bacterial growth inhibition halos and bactericidal kinetic testing. The AgNPs/PVA/CM-chitosan nanofibers possessed certain antibacterial ability, which makes them capable for antibacterial biomaterials.

  6. Effect of Molecular Weight on the Thermal and Spectroscopic Properties of Poly(vinyl alcohol) Films

    International Nuclear Information System (INIS)

    Khafagy, R.M.; Abd El-Kader, K.M.; Badr, Y.A.

    2009-01-01

    Thin films of Poly(vinyl alcohol) (PVA) with molecular weights 5000, 17000,72000 and 125000 g/mol were prepared by casting technique.Samples were thermally and spectroscopically investigated using TGA, DSC, FTIR and FT-Raman spectroscopy, in order to show how the thermal stability and structure of PVA might be correlated with its molecular weight. Thermal analysis showed that samples degrade in two steps mechanism. The mechanism observed for degradation in an inert atmosphere was in accordance with the accepted mechanism of elimination followed by pyrolisation. PVA 5000MW and PVA 17000Mw showed almost similar thermal behavior due to their expected similar structure. PVA 72000Mw showed lower thermal stability since it is characterized with the presence of the unstable C-O-C ether linkages, which lead to the fast melting of this sample. PVA 125000Mw showed the highest thermal stability because crosslinking of the main chains takes place due to introducing additional PVA units, which substitute each over oxygen atom. ΔH values obtained from DSC showed good accordance with TGA and Drtg analysis. Moreover, FTIR and FT-Raman results agreed well with thermal analysis, and confirmed our supposed structural changes which might take place as the molecular weight of the sample changes: since the water uptake, presence of ether linkages, and double bonds formulation due to crosslinking, were confirmed with FTIR and FT-Raman spectral analysis. The crystallinity percentage of the samples was calculated from Raman spectra and results confirmed our spectroscopic explanations. The thermal and spectroscopic behavior of the samples was explained as a result of the competitive action of at least three factors due to increasing the molecular weight: (i) diminution of the existing physical network due to changes in hydrogen bonding; (ii) formation of a chemical network; and (iii) introduction of flexible moieties due to the specific chemical structure after crosslinking

  7. Composite Scaffold of Poly(Vinyl Alcohol) and Interfacial Polyelectrolyte Complexation Fibers for Controlled Biomolecule Delivery

    Science.gov (United States)

    Cutiongco, Marie Francene A.; Choo, Royden K. T.; Shen, Nathaniel J. X.; Chua, Bryan M. X.; Sju, Ervi; Choo, Amanda W. L.; Le Visage, Catherine; Yim, Evelyn K. F.

    2015-01-01

    Controlled delivery of hydrophilic proteins is an important therapeutic strategy. However, widely used methods for protein delivery suffer from low incorporation efficiency and loss of bioactivity. The versatile interfacial polyelectrolyte complexation (IPC) fibers have the capacity for precise spatiotemporal release and protection of protein, growth factor, and cell bioactivity. Yet its weak mechanical properties limit its application and translation into a viable clinical solution. To overcome this limitation, IPC fibers can be incorporated into polymeric scaffolds such as the biocompatible poly(vinyl alcohol) hydrogel (PVA). Therefore, we explored the use of a composite scaffold of PVA and IPC fibers for controlled biomolecule release. We first observed that the permeability of biomolecules through PVA films were dependent on molecular weight. Next, IPC fibers were incorporated in between layers of PVA to produce PVA–IPC composite scaffolds with different IPC fiber orientation. The composite scaffold demonstrated excellent mechanical properties and efficient biomolecule incorporation. The rate of biomolecule release from PVA–IPC composite grafts exhibited dependence on molecular weight, with lysozyme showing near-linear release for 1 month. Angiogenic factors were also incorporated into the PVA–IPC grafts, as a potential biomedical application of the composite graft. While vascular endothelial growth factor only showed a maximum cumulative release of 3%, the smaller PEGylated-QK peptide showed maximum release of 33%. Notably, the released angiogenic biomolecules induced endothelial cell activity thus indicating retention of bioactivity. We also observed lack of significant macrophage response against PVA–IPC grafts in a rabbit model. Showing permeability, mechanical strength, precise temporal growth factor release, and bioinertness, PVA–IPC fibers composite scaffolds are excellent scaffolds for controlled biomolecule delivery in soft tissue

  8. Submillimeter Diameter Poly(Vinyl Alcohol) Vascular Graft Patency in Rabbit Model

    Science.gov (United States)

    Cutiongco, Marie F. A.; Kukumberg, Marek; Peneyra, Jonnathan L.; Yeo, Matthew S.; Yao, Jia Y.; Rufaihah, Abdul Jalil; Le Visage, Catherine; Ho, Jackie Pei; Yim, Evelyn K. F.

    2016-01-01

    Microvascular surgery is becoming a prevalent surgical practice. Replantation, hand reconstruction, orthopedic, and free tissue transfer procedures all rely on microvascular surgery for the repair of venous and arterial defects at the millimeter and submillimeter levels. Often, a vascular graft is required for the procedure as a means to bridge the gap between native arteries. While autologous vessels are desired for their bioactivity and non-thrombogenicity, the tedious harvest process, lack of availability, and caliber or mechanical mismatch contribute to graft failure. Thus, there is a need for an off-the-shelf artificial vascular graft that has low thrombogenic properties and mechanical properties matching those of submillimeter vessels. Poly(vinyl alcohol) hydrogel (PVA) has excellent prospects as a vascular graft due to its bioinertness, low thrombogenicity, high water content, and tunable mechanical properties. Here, we fabricated PVA grafts with submillimeter diameter and mechanical properties that closely approximated those of the rabbit femoral artery. In vitro platelet adhesion and microparticle release assay verified the low thrombogenicity of PVA. A stringent proof-of-concept in vivo test was performed by implanting PVA grafts in rabbit femoral artery with multilevel arterial occlusion. Laser Doppler measurements indicated the improved perfusion of the distal limb after implantation with PVA grafts. Moreover, ultrasound Doppler and angiography verified that the submillimeter diameter PVA vascular grafts remained patent for 2 weeks without the aid of anticoagulant or antithrombotics. Endothelial cells were observed in the luminal surface of one patent PVA graft. The advantageous non-thrombogenic and tunable mechanical properties of PVA that are retained even in the submillimeter diameter dimensions support the application of this biomaterial for vascular replacement in microvascular surgery. PMID:27376059

  9. Photochemical synthesis of copper nanoparticles incorporated in poly(vinyl pyrrolidone)

    International Nuclear Information System (INIS)

    Giuffrida, Salvatore; Costanzo, Lucia L.; Ventimiglia, Giorgio; Bongiorno, Corrado

    2008-01-01

    The effect of the presence of poly(vinyl pyrrolidone) (PVP) on the copper nanoparticle formation, obtained by UV irradiation of ethanol solution of Cu(acac) 2 (acac = 2,4-pentanedionato), was investigated. At 254 nm, in conditions of light completely absorbed by complex, the PVP exhibited protective and stabilizing effects, as shown by the formation of a colloidal copper solution and by a block of the heterogeneous process, which leads to thin film formation on the quartz walls. The colloidal solution was tested for several months by plasmon position and it was found that it remained unaltered in inert atmosphere, but returned to the starting complex on contact with air. The PVP ability to control the particle size was investigated by carrying out photoreduction sensitized by Hacac at 254 and 300 nm, in the presence of PVP concentration varying from 0 to 0.2 M. In this range it was possible to obtain copper nanoparticles of dimensions decreasing from 30 to 4 nm. Besides this, the PVP (0.005-0.05 M) role as sensitizer was investigated by irradiating solutions of Cu(acac) 2 at 300 nm which is an inactive wavelength for copper reduction by direct light absorption. It was found that the PVP was an efficient sensitizer of the copper photoreduction. The nanoparticles were characterized by plasmon band, Trasmission Electron Microscope (TEM) as well as Dynamic Light Scattering (DSL) analysis. The overall results evidence the advantages of the PVP use in the nanoparticle copper formation through the photochemical technique such as the exclusive formation of colloidal copper, their size control, stable colloidal solution and complete return to the starting complex.

  10. Poly(vinyl alcohol) hydrogel coatings with tunable surface exposure of hydroxyapatite

    Science.gov (United States)

    Moreau, David; Villain, Arthur; Ku, David N; Corté, Laurent

    2014-01-01

    Insufficient bone anchoring is a major limitation of artificial substitutes for connective osteoarticular tissues. The use of coatings containing osseoconductive ceramic particles is one of the actively explored strategies to improve osseointegration and strengthen the bone-implant interface for general tissue engineering. Our hypothesis is that hydroxyapatite (HA) particles can be coated robustly on specific assemblies of PVA hydrogel fibers for the potential anchoring of ligament replacements. A simple dip-coating method is described to produce composite coatings made of microscopic hydroxyapatite (HA) particles dispersed in a poly(vinyl alcohol) (PVA) matrix. The materials are compatible with the requirements for implant Good Manufacturing Practices. They are applied to coat bundles of PVA hydrogel fibers used for the development of ligament implants. By means of optical and electronic microscopy, we show that the coating thickness and surface state can be adjusted by varying the composition of the dipping solution. Quantitative analysis based on backscattered electron microscopy show that the exposure of HA at the coating surface can be tuned from 0 to over 55% by decreasing the weight ratio of PVA over HA from 0.4 to 0.1. Abrasion experiments simulating bone-implant contact illustrate how the coating cohesion and wear resistance increase by increasing the content of PVA relative to HA. Using pullout experiments, we find that these coatings adhere well to the fiber bundles and detach by propagation of a crack inside the coating. These results provide a guide to select coated implants for anchoring artificial ligaments. PMID:25482413

  11. Inhibition of nucleation and growth of ice by poly(vinyl alcohol) in vitrification solution.

    Science.gov (United States)

    Wang, Hai-Yan; Inada, Takaaki; Funakoshi, Kunio; Lu, Shu-Shen

    2009-08-01

    Control of ice formation is crucial in cryopreservation of biological substances. Successful vitrification using several additives that inhibit ice nucleation in vitrification solutions has previously been reported. Among these additives, here we focused on a synthetic polymer, poly(vinyl alcohol) (PVA), and investigated the effects of PVA on nucleation and growth of ice in 35% (w/w) aqueous 1,2-propanediol solution by using a differential scanning calorimetry (DSC) system equipped with a cryomicroscope. First, the freezing temperature of the solution was measured using the DSC system, and then the change in ice fraction in the solution during cooling was evaluated based on images obtained using the cryomicroscope, at different concentrations of PVA between 0% and 3% (w/w). Based on the ice fraction, the change in residual solution concentration during cooling was also evaluated and then plotted on the state diagram of aqueous 1,2-propanediol solution. Results indicated that, when the partially glassy and partially frozen state was intentionally allowed, the addition of PVA effectively inhibited not only ice nucleation but also ice growth in the vitrification solution. The effect of PVA on ice growth in the vitrification solution was explained based on kinetic limitations mainly due to mass transport. The interfacial kinetics also might limit ice growth in the vitrification solution only when the ice growth rate decreased below a critical value. This coincides with the fact that PVA exhibits a unique antifreeze activity in the same manner as antifreeze proteins when ice growth rate is lower than a critical value.

  12. Preparation and characterization of jackfruit seed starch/poly (vinyl alcohol) (PVA) blend film

    Science.gov (United States)

    Sarifuddin, N.; Shahrim, N. A.; Rani, N. N. S. A.; Zaki, H. H. M.; Azhar, A. Z. A.

    2018-01-01

    From the environmental point of view, biodegradable materials have been rapidly developed in the past years. PVA is one of the biodegradable synthetic polymers commonly used, but its degradation rate is slow. As an alternative to reduce plastic waste and accelerate the degradation process, PVA frequently blended with other natural polymers to improve its biodegradability. The natural polymer such as starch has high potential in enhancing PVA biodegradability by blending both components. The usage of starch extracted from agriculture wastes such as jackfruit seed is quite promising. In this study, jackfruit seed starch (JFSS)/poly (vinyl alcohol) (PVA) blend films were prepared using the solution casting method. The effect of starch content on the mechanical (tensile strength and elongation to break %) and physical properties of the tested films were investigated. The optimum tensile strength was obtained at 10.45 MPa when 4 wt. % of starch added to the blend. But, decreasing trend of tensile strength was found upon increasing the amount of starch beyond 4 wt. % in starch/PVA blend films. Nevertheless, elongation at break decreases with the increase in starch content. The mechanical properties of the blend films are supported by the Field Emission Scanning Electron Microscopy (FESEM), in which the native JFSS granules are wetted by PVA continuous phase with good dispersion and less agglomeration. The incorporation of JFSS in PVA has also resulted in the appearance of hydrogen bond peak, which evidenced by Fourier Transform Infrared (FTIR). Additionally, the biodegradation rate of JFSS/PVA was evaluated through soil burial test.

  13. Composite scaffold of poly(vinyl alcohol) and interfacial polyelectrolyte complexation fibers for controlled biomolecule delivery.

    Science.gov (United States)

    Cutiongco, Marie Francene A; Choo, Royden K T; Shen, Nathaniel J X; Chua, Bryan M X; Sju, Ervi; Choo, Amanda W L; Le Visage, Catherine; Yim, Evelyn K F

    2015-01-01

    Controlled delivery of hydrophilic proteins is an important therapeutic strategy. However, widely used methods for protein delivery suffer from low incorporation efficiency and loss of bioactivity. The versatile interfacial polyelectrolyte complexation (IPC) fibers have the capacity for precise spatiotemporal release and protection of protein, growth factor, and cell bioactivity. Yet its weak mechanical properties limit its application and translation into a viable clinical solution. To overcome this limitation, IPC fibers can be incorporated into polymeric scaffolds such as the biocompatible poly(vinyl alcohol) hydrogel (PVA). Therefore, we explored the use of a composite scaffold of PVA and IPC fibers for controlled biomolecule release. We first observed that the permeability of biomolecules through PVA films were dependent on molecular weight. Next, IPC fibers were incorporated in between layers of PVA to produce PVA-IPC composite scaffolds with different IPC fiber orientation. The composite scaffold demonstrated excellent mechanical properties and efficient biomolecule incorporation. The rate of biomolecule release from PVA-IPC composite grafts exhibited dependence on molecular weight, with lysozyme showing near-linear release for 1 month. Angiogenic factors were also incorporated into the PVA-IPC grafts, as a potential biomedical application of the composite graft. While vascular endothelial growth factor only showed a maximum cumulative release of 3%, the smaller PEGylated-QK peptide showed maximum release of 33%. Notably, the released angiogenic biomolecules induced endothelial cell activity thus indicating retention of bioactivity. We also observed lack of significant macrophage response against PVA-IPC grafts in a rabbit model. Showing permeability, mechanical strength, precise temporal growth factor release, and bioinertness, PVA-IPC fibers composite scaffolds are excellent scaffolds for controlled biomolecule delivery in soft tissue engineering.

  14. A facile method for electrospinning of Ag nanoparticles/poly (vinyl alcohol)/carboxymethyl-chitosan nanofibers

    International Nuclear Information System (INIS)

    Zhao, Yinghui; Zhou, Ying; Wu, Xiaomian; Wang, Lu; Xu, Ling; Wei, Shicheng

    2012-01-01

    Highlights: ► AgNPs/PVA/CM-chitosan nanofibers were prepared via electrospinning method. ► AgNPs were in situ synthesized in electrospinning solution via a facile method. ► AgNPs distributed homogeneously on the surface of nanofibers. ► The prepared nanofibers possessed certain antibacterial ability against Escherichia coli. ► The AgNPs containing nanofibers had potential as antibacterial biomaterial. - Abstract: A facile method to prepare silver nanoparticles (AgNPs) containing nanofibers via electrospinning has been demonstrated. AgNPs were in situ synthesized in poly (vinyl alcohol) (PVA)/carboxymethyl-chitosan (CM-chitosan) blend aqueous solution before electrospinning. UV–vis spectra, viscosity and conductivity of the electrospinning solution were measured to investigate their effects on the electrospinning procedure. The morphology of AgNPs/PVA/CM-chitosan nanofibers was observed by Field Emission Scanning Electron Microscopy. The formation and morphology of AgNPs were investigated by Transmission Electron Microscopy and X-ray Photoelectron Spectroscopy. The resulted nanofibers have smooth surface and uniform diameters ranging from 295 to 343 nm. The diameters of AgNPs mainly distributed in the range of 4–14 nm, and the electrostatic interaction between AgNPs and fibers was observed. Finally, in vitro Ag release from the nanofibers was measured and the antibacterial behavior of the nanofibers against Escherichia coli was studied by bacterial growth inhibition halos and bactericidal kinetic testing. The AgNPs/PVA/CM-chitosan nanofibers possessed certain antibacterial ability, which makes them capable for antibacterial biomaterials.

  15. Combination effect of melamine polyphosphate and graphene on flame retardant properties of poly(vinyl alcohol)

    International Nuclear Information System (INIS)

    Huang Guobo; Liang Huading; Wang Yong; Wang Xu; Gao Jianrong; Fei Zhengdong

    2012-01-01

    Highlights: ► PVA/graphene/MPP composites were prepared by solvent blending. ► PVA/graphene systems improved the flame retardancy of the nanocomposites. ► Flame retardation mechanism was explained by SEM, FT-IR and XPS. - Abstract: A novel flame retardant poly(vinyl alcohol) (PVA)/melamine polyphosphate (MPP)–graphene nanocomposite has been prepared by solvent blending. Results from X-ray diffraction (XRD) and transmission electron microscopy (TEM) suggest that an excellent dispersion of exfoliated graphene and MPP in the PVA matrix was achieved. The thermal and flammability properties of the nanocomposite were investigated using thermogravimetry, cone calorimetry, and flammability tests (UL 94 and LOI). The presence of both MPP and graphene in the polymer matrix led to an enhanced thermal stability and significantly reduced flammability for the nanocomposite. PVA composites filled with 10 wt% MPP and 1 wt% graphene (PVA/G1/MPP10) achieved the LOI value of 29.6 and UL-94 V0 grade. Compared to pure PVA, the peak heat release rate (PHRR) of PVA/G1/MPP10 is reduced by about 60%. Meanwhile, the mechanical properties of PVA/G1/MPP10 composites exhibit almost no deterioration compared with pure PVA. The morphology and composition of residues generated after cone calorimeter tests were investigated by scanning electronic microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS). The SEM images showed the compact and dense intumescent char jammed with graphene sheets was formed for PVA/G1/MPP10 during combustion. The results of XPS confirmed that carbon content of the char for PVA/G1/MPP10 is increased obviously by the combination effect of the flame retardant MPP and graphene.

  16. Oil recovery with sulfomethylated poly (lower alkyl vinyl ether/maleic anhydride)

    Energy Technology Data Exchange (ETDEWEB)

    Norton, C.J.; Falk, D.O.

    1973-05-22

    Lower alkyl vinyl ether e.g., methyl vinyl ether, propyl vinyl ether, isopropyl vinyl ether, hexyl vinyl ether, is copolymerized conventionally with maleic anhydride, the resulting copolymer is treated with ammonia or ammonium hydroxide to form the partial amide-ammonium salt, and this salt is in turn treated with formaldehyde and thereafter or simultaneously with ammonium or alkali metal salt sulfite (including bisulfites, etc.) to form an at least partially sulfomethylated copolymer. Aqueous solutions of the sulfomethylated copolymer are useful in increasing the viscosity of drive fluids used in the supplemented recovery of petroleum from subterranean formations. In general, enhancing the polyionic character of mobility control agents used in supplemented recovery of petroleum provides enhanced recovery. Achieving this enhancement of polyionic character through use of sulfonate groups provides a mobility control agent with good ability to sustain viscosity in the presence of brine and lime, usually present in the connate waters of petroleum-bearing formations. (7 claims)

  17. Preparation of poly(vinyl alcohol)-grafted graphene oxide/poly(vinyl alcohol) nanocomposites via in-situ low-temperature emulsion polymerization and their thermal and mechanical characterization

    International Nuclear Information System (INIS)

    Zhang, Shengchang; Liu, Pengqing; Zhao, Xiangsen; Xu, Jianjun

    2017-01-01

    Highlights: • In-situ emulsion polymerization and alcoholysis reaction is a good method to prepare GO/PVA nanocomposites. • Surface chemical grafting modification of GO with PVA chains was also carried out during the in-situ emulsion polymerization and alcoholysis reaction. • The surface chemical grafting modification of GO by in-situ polymerization and alcoholysis reaction could not only improve the dispersion of fillers in matrix, but also the interfacial interactions between fillers and matrix. • The thermal and mechanical properties of PVA-g-GO/PVA nanocompistes were also studied. - Abstract: An in-situ polymerization combined with chemical grafting modification method for preparing Poly(vinyl alcohol)-grafted graphene oxide/Poly(vinyl alcohol) (PVA-g-GO/PVA) nanocomposites was reported. Firstly, Poly(vinyl acetate)-grafted graphene oxide/Poly(vinyl acetate) nanocomposites were prepared, and then the PVA-g-GO/PVA nanocomposites could be obtained through alcoholysis reaction. X-ray photoelectron spectrometer and fourier-transform infrared spectrometer confirmed that the PVAc or PVA chains were successfully grafted to GO sheets during in-situ polymerization and alcoholysis. And the results from transmission electron microscopy, scanning electron microscopy and X-ray diffraction showed that the well compatibility and homogenous dispersion of PVA-g-GO in PVA matrix could be achieved. Differential scanning calorimetric, thermogravimetry analysis and tensile test were employed to study the thermal and mechanical properties of the PVA-g-GO/PVA nanocomposites. The results indicated that a 53% improvement of tensile strength and a 36% improvement of Young’s modulus were achieved by addition of 0.5 wt% of GO sheets. And the glass transition temperature of PVA-g-GO/PVA nanocomposites was increased, and their thermal stability and crystallization degree were both decreased. Due to well dispersion of fillers and strong interfacial interactions at the filler

  18. Preparation of poly(vinyl alcohol)-grafted graphene oxide/poly(vinyl alcohol) nanocomposites via in-situ low-temperature emulsion polymerization and their thermal and mechanical characterization

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Shengchang; Liu, Pengqing, E-mail: liupq@scu.edu.cn; Zhao, Xiangsen; Xu, Jianjun, E-mail: xujj@scu.edu.cn

    2017-02-28

    Highlights: • In-situ emulsion polymerization and alcoholysis reaction is a good method to prepare GO/PVA nanocomposites. • Surface chemical grafting modification of GO with PVA chains was also carried out during the in-situ emulsion polymerization and alcoholysis reaction. • The surface chemical grafting modification of GO by in-situ polymerization and alcoholysis reaction could not only improve the dispersion of fillers in matrix, but also the interfacial interactions between fillers and matrix. • The thermal and mechanical properties of PVA-g-GO/PVA nanocompistes were also studied. - Abstract: An in-situ polymerization combined with chemical grafting modification method for preparing Poly(vinyl alcohol)-grafted graphene oxide/Poly(vinyl alcohol) (PVA-g-GO/PVA) nanocomposites was reported. Firstly, Poly(vinyl acetate)-grafted graphene oxide/Poly(vinyl acetate) nanocomposites were prepared, and then the PVA-g-GO/PVA nanocomposites could be obtained through alcoholysis reaction. X-ray photoelectron spectrometer and fourier-transform infrared spectrometer confirmed that the PVAc or PVA chains were successfully grafted to GO sheets during in-situ polymerization and alcoholysis. And the results from transmission electron microscopy, scanning electron microscopy and X-ray diffraction showed that the well compatibility and homogenous dispersion of PVA-g-GO in PVA matrix could be achieved. Differential scanning calorimetric, thermogravimetry analysis and tensile test were employed to study the thermal and mechanical properties of the PVA-g-GO/PVA nanocomposites. The results indicated that a 53% improvement of tensile strength and a 36% improvement of Young’s modulus were achieved by addition of 0.5 wt% of GO sheets. And the glass transition temperature of PVA-g-GO/PVA nanocomposites was increased, and their thermal stability and crystallization degree were both decreased. Due to well dispersion of fillers and strong interfacial interactions at the filler

  19. Poly(mono/diethylene glycol n-tetradecyl ether vinyl ethers with Various Molecular Weights as Phase Change Materials

    Directory of Open Access Journals (Sweden)

    Dongfang Pei

    2018-02-01

    Full Text Available At present, research on the relationship of comb-like polymer phase change material structures and their heat storage performance is scarce. Therefore, this relationship from both micro and macro perspectives will be studied in this paper. In order to achieve a high phase change enthalpy, ethylene glycol segments were introduced between the vinyl and the alkyl side chains. A series of poly(mono/diethylene glycol n-tetradecyl ether vinyl ethers (PC14EnVEs (n = 1, 2 with various molecular weights were polymerized by living cationic polymerization. The results of PC14E1VE and PC14E2VE showed that the minimum number of carbon atoms required for side-chain crystallization were 7.7 and 7.2, which were lower than that reported in the literature. The phase change enthalpy 89 J/g (for poly(mono ethylene glycol n-tetradecyl ether vinyl ethers and 86 J/g (for poly(hexadecyl acrylate were approximately equal. With the increase of molecular weight, the melting temperature, the melting enthalpy, and the initial thermal decomposition temperature of PC14E1VE changed from 27.0 to 28.0 °C, from 95 to 89 J/g, and from 264 to 287 °C, respectively. When the number average molar mass of PC14EnVEs exceeded 20,000, the enthalpy values remained basically unchanged. The introduction of the ethylene glycol chain was conducive to the crystallization of alkyl side chains.

  20. Preparation and characterization of acrylic acid-grafted poly (vinyl alcohol) hydrogel actuators using γ-ray irradiation

    International Nuclear Information System (INIS)

    An, Sung Jun; Lim, Youn Mook; Gwon, Hui Jeong; Kim, Yun Hye; Youn, Min Ho; Nho, Young Chang; Han, Dong Hyun; Kim, Chong Yeal

    2008-01-01

    Active polymer gels expand and contract in response to certain environmental stimuli, such as the application of an electric field or a change in the pH level of the surroundings. This ability to achieve large, reversible deformations with no external mechanical loading has generated much interest in the use of these gels as biomimetic actuators and artificial muscles. In this study, poly (vinyl alcohol)(PVA) grafted acrylic acid monomer (PVA-g-AAc) hydrogels were prepared by 60 Co γ-ray irradiation and their properties such as degree of grafting and weight swelling in electrostimulation as an artificial muscle and actuator were investigated

  1. Controlled synthesis of novel 3D dendritic Bi2S3 /cross-linked poly(vinyl alcohol) nanocomposites

    International Nuclear Information System (INIS)

    Wu, W-T; Shi Lei; Pang Wenmin; Wang Yusong; Zhu Qingren; Xu Guoyong

    2006-01-01

    Novel spherical three-dimensional (3D) dendritic Bi 2 S 3 /cross-linked poly(vinyl alcohol) (PVA) nanocomposites were successfully synthesized in aqueous solution of amphiphilic polyvinylacetone (PVKA) (ketalization degree D H = 0.549), via one-step in situ decomposition of the complex [Bi(Tu) x ] 3+ under γ-ray irradiation, utilizing the controllable hydrolysis property of PVKA in acidic solution. Herein, PVA chains are obtained from the hydrolysed PVKA. These uniform 3D spherical nanocomposites have a structure similar to that found in the natural lotus leaf, where every microscale papilla on the leaf surface is covered by nanoscale papillae

  2. Characterization of Plasma-Polymerized 4-vinyl pyridine on Poly(Ethylene Terephthalate) film for anti-microbial properties

    DEFF Research Database (Denmark)

    Jiang, Juan; Winther-Jensen, Bjørn; Kjær, Erik Michael

    2005-01-01

    As an efficient way to create an anti-bacterial function on polymer surfaces, we have used plasma polymerisation to create a poly-4-vinyl-pyridine coating on the surface of a common polymer, PET, a polymerisation process that we have shown also works well on several other polymers. We have found....... The mechanical strength of the bond between the substrate and the surface layer has been tested by several methods, and the antibacterial effect of the surface layer with and without silver nano particles has been estimated by measuring electrical resistance as a function of time. The bacteria investigated were...

  3. Synthesis and characterization of CdxMn1-xS nanoparticles stabilized with poly(vinyl alcohol)

    International Nuclear Information System (INIS)

    Schatkoski, Vanessa M.; Mansur, Alexandra A.P.; Mansur, Herman S.; Gonzalez, Juan C.

    2011-01-01

    Colloidal luminescent semiconductor nanocrystals, also known as quantum dots, have attracted considerable attention due to their significant potential application. The doping of nanocrystalline semiconductors with divalent manganese ions results in new optical properties of these semimagnetic semiconductor quantum dots. In this work we report the synthesis and characterization Cd x Mn 1-x S nanoparticles using poly(vinyl alcohol) as stabilizing agent. Different fractions of Cd 2+ /Mn 2+ ions were investigated aiming the production of stable nanoparticles with different photoluminescence properties. (author)

  4. Effects of Saponification Rate on Electrooptical Properties and Morphology of Poly(vinyl alcohol)/Liquid Crystal Composite Films

    Science.gov (United States)

    Ono, Hiroshi; Kawatsuki, Nobuhiro

    1995-03-01

    The relationship between the saponification rate of poly(vinyl alcohol) (PVA), and the electrooptical properties and morphology of the PVA/liquid crystal (LC) composite films was investigated. Light transmission clazing and the LC droplet size were varied by changing the saponification rate or the blend ratio of two kinds of PVA with different saponification rates because the refractive index and surface tension could be controlled by the saponification rate of PVA. The threshold voltage decreased with increasing saponification rate though the extrapolation length was decreased. It was suggested that the electrooptical properties were strongly dependent on the droplet size.

  5. Formation of inorganic nanofibers by heat-treatment of poly(vinyl alcohol-zirconium compound hybrid nanofibers

    Directory of Open Access Journals (Sweden)

    Nakane K.

    2013-01-01

    Full Text Available Poly(vinyl alcohol-zirconium compound hybrid nanofibers (precursors were formed by electrospinning employing water as a solvent for the spinning solution. The precursors were converted into oxide (ZrO2, carbide (ZrC or nitride (ZrN nanofibers by heating them in air, Ar or N2 atmospheres. Monoclinic ZrO2 nanofibers with high-specific surface area were obtained by heat-treatment of the precursors in air. ZrC and ZrN nanofibers could be obtained below theoretical temperatures calculated from thermodynamics data.

  6. Nanofibre Electrospinning Poly(vinyl alcohol and Cellulose Composite Mats Obtained by Use of a Cylindrical Electrode

    Directory of Open Access Journals (Sweden)

    Anna Sutka

    2013-01-01

    Full Text Available A study of nanofibre composites obtained by electrospinning from poly(vinyl alcohol (PVA solutions of steam exploded hemp fibres and shives is reported. A combined treatment of steam explosion (SE, ball milling, and high-intensity ultrasound (HIUS is applied to prepare cellulose nanofibres (CNF from hemp fibres (CNF-F and shives (CNF-S. The reflectance Fourier transform infrared (FTIR ATR spectroscopy is used to analyze the obtained PVA/CNF composite mats. Morphology of the PVA/CNF composites was studied by scanning electron microscopy (SEM.

  7. Effect of side chain length and degree of polymerization on the decomposition and crystallization behaviour of chlorinated poly(vinyl ester) oligomers

    International Nuclear Information System (INIS)

    Heinze, D.; Mang, Th.; Popescu, C.; Weichold, O.

    2016-01-01

    Highlights: • Thermal behaviour of telomerized polyvinyl esters is investigated. • Thermal stability relies mainly on the contribution of side chains. • At equal molecular weights thermal stability is dictated by length of side chain. • Increasing the length of side chains improves also the packing degree of polymer. - Abstract: Four members of a homologous series of chlorinated poly(vinyl ester) oligomers CCl_3–(CH_2CH (OCO(CH_2)_mCH_3))_n–Cl with degrees of polymerization of 10 and 20 were prepared by telomerisation using carbon tetrachloride. The number of side chain carbon atoms ranges from 2 (poly(vinyl acetate) to 18 (poly(vinyl stearate)). The effect of the n-alkyl side chain length and of the degree of polymerization on the thermal stability and crystallization behaviour of the synthesized compounds was investigated. All oligomers degrade in two major steps by first losing HCl and side chains with subsequent breakdown of the backbone. The members with short side chains, up to poly(vinyl octanoate), are amorphous and show internal plasticization, whereas those with high number of side chain carbon atoms are semi-crystalline due to side-chain crystallization. A better packing for poly(vinyl stearate) is also noticeable. The glass transition and melting temperatures as well as the onset temperature of decomposition are influenced to a larger extent by the side chain length than by the degree of polymerization. Thermal stability is improved if both the size and number of side chains increase, but only a long side chain causes a significant increase of the resistance to degradation. This results in a stabilization of PVAc so that oligomers from poly(vinyl octanoate) on are stable under atmospheric conditions. Thus, the way to design stable, chlorinated PVEs oligomers is to use a long n-alkyl side chain.

  8. Effect of side chain length and degree of polymerization on the decomposition and crystallization behaviour of chlorinated poly(vinyl ester) oligomers

    Energy Technology Data Exchange (ETDEWEB)

    Heinze, D.; Mang, Th. [Aachen University of Applied Sciences, Heinrich-Mussmann-Str. 1, 52428 Jülich (Germany); Popescu, C., E-mail: crisan.popescu@kao.com [KAO Germany GmbH, Pfungstädterstr. 98-100, 64297 Darmstadt (Germany); Weichold, O., E-mail: weichold@ibac.rwth-aachen.de [Institute of Building Materials Research, Schinkelstr. 3, 52062 Aachen (Germany)

    2016-08-10

    Highlights: • Thermal behaviour of telomerized polyvinyl esters is investigated. • Thermal stability relies mainly on the contribution of side chains. • At equal molecular weights thermal stability is dictated by length of side chain. • Increasing the length of side chains improves also the packing degree of polymer. - Abstract: Four members of a homologous series of chlorinated poly(vinyl ester) oligomers CCl{sub 3}–(CH{sub 2}CH (OCO(CH{sub 2}){sub m}CH{sub 3})){sub n}–Cl with degrees of polymerization of 10 and 20 were prepared by telomerisation using carbon tetrachloride. The number of side chain carbon atoms ranges from 2 (poly(vinyl acetate) to 18 (poly(vinyl stearate)). The effect of the n-alkyl side chain length and of the degree of polymerization on the thermal stability and crystallization behaviour of the synthesized compounds was investigated. All oligomers degrade in two major steps by first losing HCl and side chains with subsequent breakdown of the backbone. The members with short side chains, up to poly(vinyl octanoate), are amorphous and show internal plasticization, whereas those with high number of side chain carbon atoms are semi-crystalline due to side-chain crystallization. A better packing for poly(vinyl stearate) is also noticeable. The glass transition and melting temperatures as well as the onset temperature of decomposition are influenced to a larger extent by the side chain length than by the degree of polymerization. Thermal stability is improved if both the size and number of side chains increase, but only a long side chain causes a significant increase of the resistance to degradation. This results in a stabilization of PVAc so that oligomers from poly(vinyl octanoate) on are stable under atmospheric conditions. Thus, the way to design stable, chlorinated PVEs oligomers is to use a long n-alkyl side chain.

  9. Enhanced proton conductivity by the influence of modified montmorillonite on poly (vinyl alcohol) based blend composite membranes

    Energy Technology Data Exchange (ETDEWEB)

    Palani, P. Bahavan, E-mail: bahavanpalani@gmail.com; Abidin, K. Sainul [Department of Physics, University College of Engineering, Anna University, Dindigul-624622 (India); Kannan, R., E-mail: rksrsrk@gmail.com [Department of Physics, University College of Engineering, Anna University, Dindigul-624622 (India); Department of Material Sciences & Engineering, Cornell University, Ithaca, NewYork-14853 (United States); Rajashabala, S. [School of Physics, Madurai Kamaraj University, Madurai-625021 (India); Sivakumar, M. [School of Physics, Alagappa University, Karaikudi-630004 (India)

    2016-05-23

    The highest proton conductivity value of 0.0802 Scm{sup −1} is obtained at 6 wt% of protonated MMT added to the PVA/PEG blends. The polymer blend composite membranes are prepared with varied concentration of Poly vinyl alcohol (PVA), Poly ethylene glycol (PEG) and Montmorillonite (MMT) by solution casting method. The Na{sup +} MMT was modified (protonated) to H{sup +} MMT with ion exchange process. The prepared membranes were characterized by using TGA, FTIR, XRD, Ion Exchange Capacity, Water/Methanol uptake, swelling ratio and proton conductivity. The significant improvements in the hydrolytic stability were observed. In addition, thermal stability of the composite membranes were improved and controlled by the addition of MMT. All the prepared membranes are shown appreciable values of proton conductivity at room temperature with 100% relative humidity.

  10. Electrospinning of poly(vinyl alcohol) nanofibers loaded with hexadecane nanodroplets.

    Science.gov (United States)

    Arecchi, A; Mannino, S; Weiss, J

    2010-08-01

    The feasibility of producing poly(vinyl alcohol) (PVA) nanofibers containing fine-disperse hexadecane droplets by electrospinning a blend of hexadecane-in-water emulsions and PVA was investigated. Hexadecane oil-in-water nanoemulsions (d(10)= 181.2 +/- 0.1 nm) were mixed with PVA at pH 4.5 to yield polymer-emulsion blends containing 0.5 to 1.5 wt% oil droplets and 8-wt% PVA. The solution properties of emulsions and emulsion-PVA blends (viscosity, conductivity, surface tension) were determined. Solutions were electrospun and the morphology and thermal properties of deposited fiber mats characterized by scanning electron microscopy and differential scanning calorimetry. Fiber mats were dissolved in buffer to liberate incorporated hexadecane droplets and the buffer solutions analyzed by optical microscopy, UV-spectroscopy, and light scattering. Analysis of dry fiber mats and their solutions showed that emulsion droplets were indeed part of the electrospun fiber structures. Depending on the concentration of hexadecane in the initial emulsion-polymer blends, droplets were dispersed in the fibers as individual droplets or in form of aggregated flocs of hexadecane droplets. Nanofibers with spindle-like perturbations or nanofibers containing bead-like structures with approximately 5 times larger than the size of droplets in the original nanoemulsion were obtained. Remarkably, incorporation of hexadecane droplets in fibers did not alter size of individual droplets, that is, no coalescence occurred. The manufacture of solid matrix containing nanodroplets could be of substantial interest for manufacturers wishing to develop encapsulation system for lipophilic functional compounds such as lipid-soluble flavors, antimicrobials, antioxidants, and bioactives with tailored release kinetics. Practical Applications: The paper describes the formation of electrospun nanofibers from hydrophilic polymers that contain fine-disperse emulsion droplets. By incorporating emulsion droplets, a

  11. Nonlinear optical properties of ZnO/poly (vinyl alcohol) nanocomposite films

    International Nuclear Information System (INIS)

    Jeeju, P. P.; Jayalekshmi, S.; Chandrasekharan, K.

    2014-01-01

    Extensive studies have already been reported on the optical characteristics of ZnO/polymer nanocomposite films, using a variety of polymers including transparent polymers such as polystyrene, polymethyl methacrylate etc and many interesting results have been established regarding the non linear optical characteristics of these systems. Poly (vinyl alcohol)(PVA) is a water soluble polymer. Though the structural and optical studies of ZnO/PVA nanocomposite films have already been investigated, there are no detailed reports on the nonlinear optical characteristics of ZnO/PVA nanocomposite films, irrespective of the fact that these nanocomposite films can be synthesized using quite easy and cost effective methods. The present work is an attempt to study in detail the nonlinear optical behaviour of ZnO/PVA nanocomposite films using Z-scan technique. Highly transparent ZnO/PVA nanocomposite films were prepared from the ZnO incorporated PVA solution in water using spin coating technique. The ZnO nanoparticles were synthesized by the simple chemical route at room temperature. High-resolution transmission electron microscopy studies show that the ZnO nanoparticles are of size around 10 nm. The ZnO/PVA nanocomposite films were structurally characterized by X-ray diffraction technique, from which the presence of both PVA and ZnO in the nanocomposite was established. The optical absorptive nonlinearity in the nanocomposite films was investigated using open aperture Z-scan technique. The results indicate optical limiting type nonlinearity in the films due to two photon absorption in ZnO with efficiency more than 50%. These films also show a self defocusing type negative nonlinear refraction in closed aperture Z-scan experiment. The present studies indicate that, highly transparent and homogeneous films of ZnO/PVA nanocomposite can be obtained on glass substrates using simple methods, in a highly cost effective way, since PVA is water soluble. These nanocomposite films offer

  12. Bio-Inspired nacre-like nanolignocellulose-poly (vinyl alcohol)-TiO2 composite with superior mechanical and photocatalytic properties.

    Science.gov (United States)

    Chen, Yipeng; Wang, Hanwei; Dang, Baokang; Xiong, Ye; Yao, Qiufang; Wang, Chao; Sun, Qingfeng; Jin, Chunde

    2017-05-12

    Nacre, the gold standard for biomimicry, provides an excellent example and guideline for assembling high-performance composites. Inspired by the layered structure and extraordinary strength and toughness of natural nacre, nacre-like nanolignocellulose/poly (vinyl alcohol)/TiO 2 composites possessed the similar layered structure of natural nacre were constructed through hot-pressing process. Poly (vinyl alcohol) and TiO 2 nanoparticles have been used as nanofillers to improve the mechanical performance and synchronously endow the superior photocatalytic activity of the composites. This research would be provided a promising candidate for the photooxidation of volatile organic compounds also combined with outstanding mechanical property.

  13. Characterization of plasma-polymerized 4-vinyl pyridine with silver nanoparticies on poly(ethylene terephthalate) film for anti-microbial properties

    DEFF Research Database (Denmark)

    Jiang, J.; Winther-Jensen, Bjørn; Kjær, Erik Michael

    2006-01-01

    scanning electron microscopy (FE-SEM), atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS). Different thicknesses Of poly(4-vinyl pyridine) coating under different plasma polymerization conditions were studied. Silver nanoparticles with diameter around 50nm deposit were precipitated...... on the poly(4-vinyl pyridine) coating by UV irradiation in Silver nitride water solution, in order to enhance the anti-microbial properties. Different kinds of modified PET films were tested for anti-microbial properties against yeast (Debaryomyces hansenii) by using microbiological analyser mu-4200...

  14. Investigation of nanocomposites made with poly(methacrylic acid-co-methyl methacrylate)/poly(N-vinyl-2-pyrrolidone)/multi-walled carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Guoqin, Liu; Wei, Miao [College of Material Science and Engineering, Henan University of Technology (China); Lin-Jian, Shangguan, E-mail: mikepolymer@126.com [School of Mechanical Engineering, North China University of Water Conservancy and Electric Power (China)

    2014-06-01

    Poly(methacrylic acid-co-methyl methacrylate) (P(MAA-co-MMA)) was prepared in the presence of poly(N-vinyl-2-pyrrolidone) (PVP) and multi-walled carbon nanotubes (MWNTs) via ultrasonic assisted solution free radical polymerization, i.e., P(MAA-co-MMA)/PVP/MWNTs nanocomposites. The morphology, glassy-state storage modulus, thermal behavior and swelling characteristics of P(MAA-co-MMA)/PVP/MWNTs nanocomposites were investigated. Scanning electron micrographs (SEM) revealed that MWNTs at low concentration could be uniformly dispersed into P(MAA-co-MMA)/PVP blends. With increasing MWNTs weight fraction, the average glassy-state modulus, glass transition temperatures and decomposition temperature of the nanocomposites increased, but their swelling characteristics decreased. (author)

  15. Investigation of nanocomposites made with poly(methacrylic acid-co-methyl methacrylate/poly(N-vinyl-2-pyrrolidone/multi-walled carbon nanotubes

    Directory of Open Access Journals (Sweden)

    Liu Guoqin

    2014-01-01

    Full Text Available Poly(methacrylic acid-co-methyl methacrylate (P(MAA-co-MMA was prepared in the presence of poly(N-vinyl-2-pyrrolidone (PVP and multiwalled carbon nanotubes (MWNTs via ultrasonic assisted solution free radical polymerization, i.e., P(MAA-co-MMA/PVP/MWNTs nanocomposites. The morphology, glassy-state storage modulus, thermal behavior and swelling characteristics of P(MAA-co-MMA/PVP/MWNTs nanocomposites were investigated. Scanning electron micrographs (SEM revealed that MWNTs at low concentration could be uniformly dispersed into P(MAA-co-MMA/PVP blends. With increasing MWNTs weight fraction, the average glassy-state modulus, glass transition temperatures and decomposition temperature of the nanocomposites increased, but their swelling characteristics decreased.

  16. Effect of Cross-Linking on the Mechanical and Thermal Properties of Poly(amidoamine Dendrimer/Poly(vinyl alcohol Hybrid Membranes for CO2 Separation

    Directory of Open Access Journals (Sweden)

    Shuhong Duan

    2014-04-01

    Full Text Available Poly(amidoamine (PAMAM dendrimers were incorporated into cross-linked poly(vinyl alcohol (PVA matrix to improve carbon dioxide (CO2 separation performance at elevated pressures. In our previous studies, PAMAM/PVA hybrid membranes showed high CO2 separation properties from CO2/H2 mixed gases. In this study, three types of organic Ti metal compounds were selected as PVA cross-linkers that were used to prepare PAMAM/cross-linked PVA hybrid membranes. Characterization of the PAMAM/cross-linked PVA hybrid membranes was conducted using nanoindentation and thermogravimetric analyses. The effects of the cross-linker and CO2 partial pressure in the feed gas on CO2 separation performance were discussed. H2O and CO2 sorption of the PAMAM/PVA hybrid membranes were investigated to explain the obtained CO2 separation efficiencies.

  17. Effect of Cross-Linking on the Mechanical and Thermal Properties of Poly(amidoamine) Dendrimer/Poly(vinyl alcohol) Hybrid Membranes for CO2 Separation.

    Science.gov (United States)

    Duan, Shuhong; Kai, Teruhiko; Saito, Takashi; Yamazaki, Kota; Ikeda, Kenichi

    2014-04-08

    Poly(amidoamine) (PAMAM) dendrimers were incorporated into cross-linked poly(vinyl alcohol) (PVA) matrix to improve carbon dioxide (CO2) separation performance at elevated pressures. In our previous studies, PAMAM/PVA hybrid membranes showed high CO2 separation properties from CO2/H2 mixed gases. In this study, three types of organic Ti metal compounds were selected as PVA cross-linkers that were used to prepare PAMAM/cross-linked PVA hybrid membranes. Characterization of the PAMAM/cross-linked PVA hybrid membranes was conducted using nanoindentation and thermogravimetric analyses. The effects of the cross-linker and CO2 partial pressure in the feed gas on CO2 separation performance were discussed. H2O and CO2 sorption of the PAMAM/PVA hybrid membranes were investigated to explain the obtained CO2 separation efficiencies.

  18. Synthesis and evaluation of water-soluble poly(vinyl alcohol)-paclitaxel conjugate as a macromolecular prodrug

    International Nuclear Information System (INIS)

    Kakinoki, Atsufumi; Kaneo, Yoshiharu; Tanaka, Tetsuro; Hosokawa, Yoshitsugu

    2008-01-01

    Paclitaxel (PTX) is an antitumor agent for the treatment of various human cancers. Cremophor EL and ethanol are used to formulate PTX in commercial injection solutions, because of its poor solubility in water. However, these agents cause severe allergic reaction upon intravenous administration. The aim of this study is to synthesize water-soluble macromolecular prodrugs of PTX for enhancing the therapeutic efficacy. Poly (vinyl alcohol) (PVA, 80 kDa), water-soluble synthetic polymer, was used as a drug carrier which is safe and stable in the body. The 2'-hydroxyl group of PTX was reacted with succinic anhydride and then carboxylic group of the succinyl spacer was coupled to PVA via ethylene diamine spacer, resulting the water-soluble prodrug of poly (vinyl alcohol)-paclitaxel conjugate (PVA-SPTX). The solubility of PTX was greatly enhanced by the conjugation to PVA. The release of PTX from the conjugate was accelerated at the neutral to basic conditions in in vitro release experiment. [ 125 I]-labeled PVA-SPTX was retained in the blood circulation for several days and was gradually distributed into the tumorous tissue after intravenous injection to the tumor-bearing mice. PVA-SPTX inhibited the growth of sarcoma 180 cells subcutaneously inoculated in mice. It was suggested that the water-solubility of PTX was markedly enhanced by the conjugation to PVA, and PVA-SPTX effectively delivered PTX to the tumorous tissue due to the enhanced permeability and retention (EPR) effect. (author)

  19. Potentiometric titration of polyhexamethylene biguanide hydrochloride with potassium poly(vinyl sulfate) solution using a cationic surfactant-selective electrode.

    Science.gov (United States)

    Masadome, Takashi; Yamagishi, Yuichi; Takano, Masaki; Hattori, Toshiaki

    2008-03-01

    A potentiometric titration method using a cationic surfactant as an indicator cation and a plasticized poly(vinyl chloride) membrane electrode sensitive to the cationic surfactant is proposed for the determination of polyhexamethylene biguanide hydrochloride (PHMB-HCl), which is a cationic polyelectrolyte. A sample solution of PHMB-HCl containing an indicator cation (hexadecyltrimethylammonium ion, HTA) was titrated with a standard solution of an anionic polyelectrolyte, potassium poly(vinyl sulfate) (PVSK). The end-point was detected as a sharp potential change due to an abrupt decrease in the concentration of the indicator cation, HTA, which is caused by its association with PVSK. The effects of the concentrations of HTA ion and coexisting electrolytes in the sample solution on the degree of the potential change at the end-point were examined. A linear relationship between the concentration of PHMB-HCl and the end-point volume of the titrant exists in the concentration range from 2.0 x 10(-5) to 4.0 x 10(-4) M in the case that the concentration of HTA is 1.0 x 10(-5) M, and that from 1.0 x 10(-6) to 1.2 x 10(-5) M in the case that the concentration of HTA is 5.0 x 10(-6) M, respectively. The proposed method was applied to the determination of PHMB-HCl in some contact-lens detergents.

  20. Mucoadhesive hydrogel microparticles based on poly (methacrylic acid-vinyl pyrrolidone)-chitosan for oral drug delivery.

    Science.gov (United States)

    Sajeesh, S; Sharma, Chandra P

    2011-05-01

    The study was aimed at the evaluation of N-vinyl pyrrolidone (NVP) incorporated polymethacrylic acid-chitosan microparticles for oral drug delivery applications. Poly (methacrylic acid)-chitosan (PMC) and poly(methacrylic acid-vinyl pyrrolidone)-chitosan (PMVC) microparticles were prepared by an ionic-gelation method. Mucoadhesion behaviour of these particles was evaluated by ex-vivo adhesion method using freshly excised rat intestinal tissue. Cytotoxicity and absorption enhancing property of PMC and PMVC particles were evaluated on Caco 2 cell monolayers. Protease enzyme inhibition capability and insulin loading/release properties of these hydrogel particles was evaluated under in vitro experimental conditions. Addition of NVP units enhanced the mucoadhesion behavior of PMC particles on isolated rat intestinal tissue. Both PMC and PMVC particles were found non-toxic on Caco 2 cell monolayers and PMC particles was more effective in improving paracellular transport of fluorescent dextran across Caco 2 cell monolayers as compared to PMVC particles. However, protease inhibition efficacy of PMC particles was not significantly affected with NVP addition. NVP incorporation improved the insulin release properties of PMC microparticles at acidic pH. Hydrophilic modification seems to be an interesting approach in improving mucoadhesion capability of PMC microparticles.

  1. Surface characterization of poly(vinyl chloride) urinary catheters functionalized with acrylic acid and poly(ethylene glycol) methacrylate using gamma-radiation

    Energy Technology Data Exchange (ETDEWEB)

    Islas, Luisa [Departamento de Química de Radiaciones y Radioquímica, Instituto de Ciencias Nucleares, Universidad Nacional Autónoma de México, Ciudad Universitaria, Mexico D.F. 04510 (Mexico); Ruiz, Juan-Carlos [División de Ciencias Básicas e Ingeniería, Depto. de Ingeniería de Procesos e Hidráulica, Universidad Autónoma Metropolitana-Iztapalapa, Av. San Rafael Atlixco No. 186, 09340 México D.F. (Mexico); Muñoz-Muñoz, Franklin [Facultad de Ingeniería, Arquitectura y Diseño, Universidad Autónoma de Baja California, Carretera Transpeninsular Ensenada-Tijuana 3917, Ensenada, B.C. C.P 22860 (Mexico); Isoshima, Takashi [Nano Medical Engineering Laboratory, RIKEN, 2-1Hirosawa, Wako, Saitama 351-0198 (Japan); Burillo, Guillermina, E-mail: burillo@nucleares.unam.mx [Departamento de Química de Radiaciones y Radioquímica, Instituto de Ciencias Nucleares, Universidad Nacional Autónoma de México, Ciudad Universitaria, Mexico D.F. 04510 (Mexico)

    2016-10-30

    Highlights: • Polymer grafting using gamma-radiation allowed for acrylic acid and poly(ethylene glycol) methacrylate to graft on the inner and outer surface of poly(vinyl chloride) urinary catheters. • HR-XPS revealed the different compositional percentages of the compounds present on the surface of the catheter. • Catheters that were grafted with PEGMA had the roughest surface as observed using scanning electron microscopy (SEM) and confocal laser microscopy (CLM). - Abstract: Poly(vinyl chloride) (PVC) urinary catheters were modified with either a single or binary graft of acrylic acid (AAc) and/or poly(ethylene glycol) methacrylate (PEGMA) using gamma-radiation from {sup 60}Co to obtain PVC-g-AAc, PVC-g-PEGMA, [PVC-g-AAc]-g-PEGMA, and [PVC-g-PEGMA]-g-AAc copolymers. The outer and inner surfaces of the modified catheters were characterized using scanning electron microscopy (SEM), confocal laser microscopy (CLM) and X-ray photoelectron spectroscopy (XPS). The XPS analyses, by examining the correlation between the variation of the C{sub 1s} and O{sub 1s} content at the catheter’s surface, revealed that the catheter’s surfaces were successfully grafted with the chosen compounds, with those that were binary grafted showing a slightly more covered surface as was evidenced by the disappearance of PVC’s Cl peak. The SEM and CLM analyses revealed that catheters that had been grafted with PEGMA had a rougher outer surface as compared to those that had only been grafted with AAc. In addition, these imaging techniques showed that the inner surface of the singly grafted catheters, whether they had been grafted with AAc or PEGMA, retained some smoothness at the analyzed grafting percentages, while the binary grafted catheters showed many protuberances and greater roughness on both outer and inner surfaces.

  2. In vitro mechanical fatigue behavior of poly-ɛ-caprolactone macroporous scaffolds for cartilage tissue engineering: Influence of pore filling by a poly(vinyl alcohol) gel.

    Science.gov (United States)

    Panadero, J A; Vikingsson, L; Gomez Ribelles, J L; Lanceros-Mendez, S; Sencadas, V

    2015-07-01

    Polymeric scaffolds used in regenerative therapies are implanted in the damaged tissue and submitted to repeated loading cycles. In the case of articular cartilage engineering, an implanted scaffold is typically subjected to long-term dynamic compression. The evolution of the mechanical properties of the scaffold during bioresorption has been deeply studied in the past, but the possibility of failure due to mechanical fatigue has not been properly addressed. Nevertheless, the macroporous scaffold is susceptible to failure after repeated loading-unloading cycles. In this work fatigue studies of polycaprolactone scaffolds were carried by subjecting the scaffold to repeated compression cycles in conditions simulating the scaffold implanted in the articular cartilage. The behavior of the polycaprolactone sponge with the pores filled with a poly(vinyl alcohol) gel simulating the new formed tissue within the pores was compared with that of the material immersed in water. Results were analyzed with Morrow's criteria for failure and accurate fittings are obtained just up to 200 loading cycles. It is also shown that the presence of poly(vinyl alcohol) increases the elastic modulus of the scaffolds, the effect being more pronounced with increasing the number of freeze/thawing cycles. © 2014 Wiley Periodicals, Inc.

  3. A novel process for separation of hazardous poly(vinyl chloride) from mixed plastic wastes by froth flotation.

    Science.gov (United States)

    Wang, Jianchao; Wang, Hui; Wang, Chongqing; Zhang, Lingling; Wang, Tao; Zheng, Long

    2017-11-01

    A novel method, calcium hypochlorite (CHC) treatment, was proposed for separation of hazardous poly(vinyl chloride) (PVC) plastic from mixed plastic wastes (MPWs) by froth flotation. Flotation behavior of single plastic indicates that PVC can be separated from poly(ethylene terephthalate) (PET), poly(acrylonitrile-co-butadiene-co-styrene) (ABS), polystyrene (PS), polycarbonate (PC) and poly(methyl methacrylate) (PMMA) by froth flotation combined with CHC treatment. Mechanism of CHC treatment was examined by contact angle measurement, scanning electron microscopy, Fourier transform infrared and X-ray photoelectron spectroscopy. Under the optimum conditions, separation of PVC from binary plastics with different particle sizes is achieved efficiently. The purity of PC, ABS, PMMA, PS and PET is greater than 96.8%, 98.5%, 98.8%, 97.4% and 96.3%, respectively. Separation of PVC from multi-plastics was further conducted by two-stage flotation. PVC can be separated efficiently from MPWs with residue content of 0.37%. Additionally, reusing CHC solution is practical. This work indicates that separation of hazardous PVC from MPWs is effective by froth flotation. Copyright © 2017 Elsevier Ltd. All rights reserved.

  4. Microencapsulation of Epoxidized Linseed Oil Liquid Cross-Linker in Poly(N-vinyl-pyrrolidone): Optimization by a Design-of-Experiments Approach

    NARCIS (Netherlands)

    Senatore, D.; Laven, J.; Benthem, van R.A.T.M.; La Camera, D.; With, de G.

    2010-01-01

    A liquid cross-linker, epoxidized linseed oil (ELO), was encapsulated in a plastic with a high glass transition temperature (poly(N-vinyl-2-pyrrolidone); PVP). The process parameters of the spray-drying employed were optimized by a Design-of-Experiments (DoE) approach. Three factors concerning both

  5. Synthesis and characterization of UV photocrosslinkable hydrogels with poly(N-vinyl-2-pyrrolidone): Determination of the network mesh size distribution

    DEFF Research Database (Denmark)

    Marizza, Paolo; Abrami, M.; Keller, Stephan Sylvest

    2016-01-01

    Hydrogels of poly(n-vinyl-2-pyrrolidone) were produced by UV irradiation of aqueous solutions of the polymer in presence of hydrogen peroxide, used as initiator. The mechanical and the nanostructural properties of the gels were characterized by a combination of experimental techniques including...

  6. Thermodynamic and kinetic analysis of phase separation of temperature-sensitive poly(vinyl methyl ether) in the presence of hydrophobic tert-butyl alcohol

    Czech Academy of Sciences Publication Activity Database

    Velychkivska, Nadiia; Bogomolova, Anna; Filippov, Sergey K.; Starovoytova, Larisa; Labuta, J.

    2017-01-01

    Roč. 295, č. 8 (2017), s. 1419-1428 ISSN 0303-402X R&D Projects: GA ČR(CZ) GC15-10527J Institutional support: RVO:61389013 Keywords : phase separation * coil-globule transition * poly(vinyl methyl ether) Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry Impact factor: 1.723, year: 2016

  7. Synthesis and application of a novel environmental C26 diglycidyl ester plasticizer based on castor oil for poly(vinyl chloride)

    Science.gov (United States)

    In this work, for the first time, a castor oil derived diglycidyl ester plasticizer (C26-DGE) was prepared and incorporated into poly(vinyl chloride) (PVC). The chemical structure of the product was characterized by Fourier transform infrared spectroscopy (FT-IR), proton nuclear magnetic resonance (...

  8. Uranium Adsorbent Fibers Prepared by Atom-Transfer Radical Polymerization (ATRP) from Poly(vinyl chloride)- co -chlorinated Poly(vinyl chloride) (PVC- co -CPVC) Fiber

    Energy Technology Data Exchange (ETDEWEB)

    Brown, Suree; Yue, Yanfeng; Kuo, Li-Jung; Mehio, Nada; Li, Meijun; Gill, Gary; Tsouris, Costas; Mayes, Richard T.; Saito, Tomonori; Dai, Sheng

    2016-04-20

    The need to secure future supplies of energy attracts researchers in several countries to a vast resource of nuclear energy fuel: uranium in seawater (estimated at 4.5 billion tons in seawater). In this study, we developed effective adsorbent fibers for the recovery of uranium from seawater via atom-transfer radical polymerization (ATRP) from a poly- (vinyl chloride)-co-chlorinated poly(vinyl chloride) (PVC-co-CPVC) fiber. ATRP was employed in the surface graft polymerization of acrylonitrile (AN) and tert-butyl acrylate (tBA), precursors for uranium-interacting functional groups, from PVC-co-CPVC fiber. The [tBA]/[AN] was systematically varied to identify the optimal ratio between hydrophilic groups (from tBA) and uranyl-binding ligands (from AN). The best performing adsorbent fiber, the one with the optimal [tBA]/[AN] ratio and a high degree of grafting (1390%), demonstrated uranium adsorption capacities that are significantly greater than those of the Japan Atomic Energy Agency (JAEA) reference fiber in natural seawater tests (2.42-3.24 g/kg in 42 days of seawater exposure and 5.22 g/kg in 49 days of seawater exposure, versus 1.66 g/kg in 42 days of seawater exposure and 1.71 g/kg in 49 days of seawater exposure for JAEA). Adsorption of other metal ions from seawater and their corresponding kinetics were also studied. The grafting of alternative monomers for the recovery of uranium from seawater is now under development by this versatile technique of ATRP.

  9. Preparation of micro-pored silicone elastomer through radiation crosslinking

    International Nuclear Information System (INIS)

    Gao Xiaoling; Gu Mei; Xie Xubing; Huang Wei

    2013-01-01

    The radiation crosslinking was adopted to prepare the micro-pored silicone elastomer, which was performed by vulcanization and foaming respectively. Radiation crosslinking is a new method to prepare micro-pored material with high performance by use of radiation technology. Silicon dioxide was used as filler, and silicone elastomer was vulcanized by electron beams, then the micro-pored material was made by heating method at a high temperature. The effects of absorbed dose and filler content on the performance and morphology were investigated. The structure and distribution of pores were observed by SEM. The results show that the micro-pored silicon elastomer can be prepared successfully by controlling the absorbed dose and filler content. It has a smooth surface similar to a rubber meanwhile the pores are round and unconnected to each other with the minimum size of 14 μm. And the good mechanical performance can be suitable for further uses. (authors)

  10. Fabrication and characterization of a novel hydrophobic CaCO{sub 3} grafted by hydroxylated poly(vinyl chloride) chains

    Energy Technology Data Exchange (ETDEWEB)

    Bao, Lixia [State Key Laboratory of Polymer Materials Engineering, Sichuan University (China); School of Chemical Science and Technology, Yunnan University (China); Yang, Simei; Luo, Xin [School of Chemical Science and Technology, Yunnan University (China); Lei, Jingxin [State Key Laboratory of Polymer Materials Engineering, Sichuan University (China); Cao, Qiue [School of Chemical Science and Technology, Yunnan University (China); Wang, Jiliang, E-mail: jlwang@ynu.edu.cn [School of Chemical Science and Technology, Yunnan University (China)

    2015-12-01

    Highlights: • Hydroxylated poly(vinyl chloride) (PVC-OH) with different molecular weight and hydroxyl value was successfully prepared by the suspension copolymerization. • PVC-OH was grafted onto the surface of CaCO{sub 3} particles by the urethane formation reaction. • The modified CaCO{sub 3} particles show excellent hydrophobicity. - Abstract: The hydroxylated PVC (PVC-OH) was successfully synthesized by a suspension polymerization of vinyl chloride (VC), butyl acrylate (BA) and hydroxyethyl acrylate (HEA). Novel hydrophobic CaCO{sub 3} was then prepared by a urethane formation reaction between methylene diphenyl diisocyanate (MDI) and the −OH groups both in the PVC-OH chains and on the surface of pristine CaCO{sub 3} particles. The effect of the PVC-OH content on the grafting ratio of treated CaCO{sub 3} particles was extensively investigated. Combining the result of Fourier transform infrared (FTIR) with that of water contact angle, it can be concluded that the hydrophobicity of CaCO{sub 3} had been efficiently improved by the PVC-OH segments grafted on the surface of CaCO{sub 3} particles. X-ray diffraction (XRD), thermal gravity analysis (TGA), scanning electron microscope (SEM) and transmission electron microscope (TEM) were also used to study crystalline behaviors, thermal stability and surface morphology of the modified CaCO{sub 3} particles, respectively. The change of specific surface area implying surface modification was investigated as well.

  11. Fabrication of thermo-responsive cotton fabrics using poly(vinyl caprolactam-co-hydroxyethyl acrylamide) copolymer.

    Science.gov (United States)

    Xiao, Min; González, Edurne; Monterroza, Alexis Martell; Frey, Margaret

    2017-10-15

    A thermo-responsive polymer with hydrophilic to hydrophobic transition behavior, poly(vinyl caprolactam-co-hydroxyethyl acrylamide) P(VCL-co-HEAA), was prepared by copolymerization of vinyl caprolactam and N-hydroxyethyl acrylamide via free radical solution polymerization. The resulting copolymer was characterized by Fourier transform infrared spectroscopy (FTIR), 1 H nuclear magnetic resonance (NMR), gel permeation chromatography (GPC), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). The lower critical solution temperature (LCST) of P(VCL-co-HEAA) was determined at 34.5°C. This thermo-responsive polymer was then grafted onto cotton fabrics using 1,2,3,4-butanetetracarboxylic acid (BTCA) as crosslinker and sodium hypophosphite (SHP) as catalyst. FTIR and energy dispersive X-ray spectroscopy (EDS) studies confirmed the successful grafting reaction. The modified cotton fabric exhibited thermo-responsive behavior as evidenced by water vapor permeability measurement confirming decreased permeability at elevated temperature. This is the first demonstration that a PVCL based copolymer is grafted to cotton fabrics. This study provides a new thermo-responsive polymer for fabrication of smart cotton fabrics with thermally switchable hydrophilicity. Copyright © 2017 Elsevier Ltd. All rights reserved.

  12. An organic dye-polymer (phenol red-poly (vinyl alcohol)) composite architecture towards tunable -optical and -saturable absorption characteristics

    Energy Technology Data Exchange (ETDEWEB)

    Sreedhar, Sreeja, E-mail: sreejasreedhar83@gmail.com; Muneera, C. I., E-mail: drcimuneera@hotmail.com [Department of Physics, University of Kerala, Kariavattom, Thiruvananthapuram 695581, Kerala (India); Illyaskutty, Navas [Institute for Sensorics and Information Systems (ISIS), Karlsruhe University of Applied Sciences, Moltkestr. 30, D-76133 Karlsruhe (Germany); Sreedhanya, S. [School of Chemical Sciences, M. G. University, Kottayam, Kerala 686560 (India); Philip, Reji [Light and Matter Physics Group, Raman Research Institute, Bangalore 560080 (India)

    2016-05-21

    Herein, we demonstrate that blending an organic dye (guest/filler), with a vinyl polymer (host template), is an inexpensive and simple approach for the fabrication of multifunctional photonic materials which could display an enhancement in the desirable properties of the constituent materials and, at the same time provide novel synergistic properties for the guest-host system. A new guest-host nanocomposite system comprising Phenol Red dye and poly (vinyl alcohol) as guest and host template, respectively, which exhibits tunable optical characteristics and saturable absorption behavior, is introduced. The dependence of local electronic environment provided by the polymer template and the interactions of the polymer molecules with the encapsulated guest molecules on the observed optical/nonlinear absorption behavior is discussed. An understanding of the tunability of the optical/ photophysical processes, with respect to the filler content, as discussed herein could help in the design of improved optical materials for several photonic device applications like organic light emitting diodes and saturable absorbers.

  13. Preparation and characterization of antibacterial electrospun chitosan/poly (vinyl alcohol)/graphene oxide composite nanofibrous membrane

    Science.gov (United States)

    Yang, Shuai; Lei, Peng; Shan, Yujuan; Zhang, Dawei

    2018-03-01

    In this paper, chitosan (CS)/poly (vinyl alcohol) (PVA)/graphene oxide (GO) composite nanofibrous membranes were prepared via electrospinning. Such nanofibrous membranes have been characterized and investigated for their morphological, structural, thermal stability, hydrophilic and antibacterial properties. SEM images showed that the uniform and defect-free nanofibers were obtained and GO sheets, shaping spindle and spherical, were partially embedded into nanofibers. FTIR, XRD, DSC and TGA indicated the good compatibility between CS and PVA. There were strong intermolecular hydrogen bonds between the chitosan and PVA molecules. Contact angle measurement indicated that while increasing the content of GO, the distance between fibers increased and water drop showed wetting state on the surface of nanofibrous membranes. As a result, the contact angle decreased significantly. Meanwhile, good antibacterial activity of the prepared nanofibrous membranes were exhibited against Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus.

  14. Synthesis and characterization of particles derived of poly(vinyl alcohol) (PVA) for treatment of embolization and chemoembolization

    International Nuclear Information System (INIS)

    Semenzim, Vinicius L.; Basso, Glaucia G.; Passos, Rodrigo A.; Nery, Jose G.; Agreli, Guilherme; Oliveira, Ana P.M.L.; Kawasaki-Oyama, Rosa S.; Braile, Domingo M.

    2009-01-01

    The most effective way to treat cancerous tumors is by surgically removing them. However in some types of cancer, such as liver and uterine cancer, more than two-thirds of patients have no indication for surgery due to the size and location of the tumor, such as into the blood vessels. Doctors and researchers have invested in alternative and less invasive methods such as chemoembolization. The objectives of this research project are the synthesis and characterization of poly(vinyl alcohol) (PVA) particles for use in cancer treatment. PVA particles will be combined with chemotherapeutic agent Doxorubicin, drug commonly used in the treatment of cancers and carcinomas. The particles, obtained by controlled polymerization reaction followed by saponification, were characterized by SEM, XRD and NMR-CP/MAS. The functionalization of the particles with the drug is the next step of this study. (author)

  15. Radiation preparation of drug carriers based polyacrylic acid (PAAc) using poly(vinyl pyrrolidone) (PVP) as a template polymer

    Science.gov (United States)

    Abd El-Rehim, H. A.; Hegazy, E. A.; Khalil, F. H.; Hamed, N. A.

    2007-01-01

    The present study deals with the radiation synthesis of stimuli response hydrophilic polymers from polyacrylic acid (PAAc). To maintain the property of PAAc and control the water swellibility for its application as a drug delivery system, radiation polymerization of AAc in the presence of poly(vinyl pyrrolidone) (PVP) as a template polymer was carried out. Characterization of the prepared PAA/PVP inter-polymer complex was investigated by determining gel content, swelling property, hydrogel microstructure and the release rate of caffeine as a model drug. The release rate of caffeine from the PAA/PVP inter-polymer complexes showed pH-dependency, and seemed to be mainly controlled by the dissolution rate of the complex above a p Ka of PAAc. The prepared inter-polymer complex could be used for application as drug carriers.

  16. Dynamic mechanical properties of polymer blends of polypropylene and poly(ethylene-co-vinyl acetate) irradiated with fast electrons

    International Nuclear Information System (INIS)

    Mihaylova, M.; Kresteva, M.; Perena, J; Phillips, P.

    2001-01-01

    Extruded blends of polypropylene and poly(ethylene-co-vinyl acetate) irradiated with fast electrons were studied. The dynamic mechanical properties were investigated with respects to the blend composition and irradiation dose. Two glass transition temperatures corresponding to the glass transitions of the pure components were observed. Their existence is an evidence of immiscibility of the components. Nevertheless, the peaks broadening, the single jump in the storage modulus values and the changes of T g with the blend ratio suggest the creation of an interface region, leading to the improvement of the compatibility of the components. The irradiation with fast electrons at doses higher than 100 KGy results in single T g transition because of the broadening of the interface layer. (authors)

  17. Comparison Study On Sunlight Or Gamma Radiation Aging Resistance Of Poly (Vinyl Pyrrolidone) Aqueous Solution With PVP Nanogel

    International Nuclear Information System (INIS)

    Doan Binh; Pham Thu Hong; Nguyen Nguyet Dieu; Nguyen Thanh Duoc

    2011-01-01

    Comparison study on sunlight or gamma-radiation aging resistance of poly (vinyl pyrrolidone) (PVP) aqueous solution with PVP nanogel at 0.5% was carried out. Sunlight or gamma- radiation aging resistance of PVP aqueous solution and nanogel was evaluated on the basis of their intrinsic viscosity, UV-VIS absorbance, weight averaged molecular weight (M w ). The PVP aqueous solution and nanogel exposed to sunlight in the storage duration of 3 months and to gamma radiation at absorbed doses of 0, 15, 30, 50 kGy were used for this study. Furthermore, the stability of PVP nanogel and of PVP aqueous solution was also studied on the change of their intrinsic viscosity, UV-VIS absorbance, weight averaged molecular weight, particle size distribution and coil size. The experimental results were shown that the aging resistance of PVP nanogel was higher than that of PVP aqueous solution when exposed to gamma radiation or sunlight. (author)

  18. Mechanical and electro-rheological properties of electrospun poly(vinyl alcohol) nanofibre mats filled with carbon black nanoparticles

    International Nuclear Information System (INIS)

    Chuangchote, Surawut; Sirivat, Anuvat; Supaphol, Pitt

    2007-01-01

    The present contribution reports, for the first time, the mechanical and electro-rheological properties of electrospun poly(vinyl alcohol) (PVA) nanofibre mats with or without the incorporation of carbon black (CB) nanoparticles. The effects of sonication and the addition of CB on morphological appearance, average diameter of the as-spun fibre mats, and that of the individual fibres, were thoroughly investigated. Incorporation of CB (1-10% based on the weight of PVA) in 10% w/v PVA solution did not affect the morphology and average diameter of the obtained fibres (∼160 nm), but it affected both the mechanical and the electro-rheological properties of the as-spun PVA/CB fibre mats, in which the mats became more rigid with the addition and increasing amount of CB

  19. Radiation preparation of graphene/carbon nanotubes hybrid fillers for mechanical reinforcement of poly(vinyl alcohol) films

    Science.gov (United States)

    Ma, Hui-Ling; Zhang, Long; Zhang, Youwei; Wang, Shuojue; Sun, Chao; Yu, Hongyan; Zeng, Xinmiao; Zhai, Maolin

    2016-01-01

    Graphene/carbon nanotubes (G/CNTs) hybrid fillers were synthesized by γ-ray radiation reduction of graphene oxide (GO) in presence of CNTs. The obtained hybrid fillers with three-dimensional (3D) interconnected network structure were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM). Poly(vinyl alcohol) (PVA) composite films with enhanced mechanical properties and thermal stability were subsequently prepared by solution blending of G/CNTs with PVA matrix. The tensile strength and Young's modulus of PVA composite films containing 1 wt% G/CNTs were measured to be 81.9 MPa and 3.9 GPa respectively, which were 56% and 33.6% higher than those of pure PVA. These substantial improvements could be attributed to the interconnected 3D structure of G/CNTs, homogeneous dispersion as well as the strong hydrogen-bonding interaction between G/CNTs and PVA macromolecular chains.

  20. Fabrication of Antibacterial Poly(Vinyl Alcohol Nanocomposite Films Containing Dendritic Polymer Functionalized Multi-Walled Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    Andreas Sapalidis

    2018-03-01

    Full Text Available A series of poly(vinyl alcohol (PVA nanocomposite films containing quaternized hyperbranched polyethyleneimine (PEI functionalized multi-walled carbon nanotubes (ox-CNTs@QPEI are prepared by solvent casting technique. The modified carbon-based material exhibits high aqueous solubility, due to the hydrophilic character of the functionalized hyperbranched dendritic polymer. The quaternized PEI successfully wraps around nanotube walls as polycations provide electrostatic repulsion. Various contents of ox-CNTs@QPEI ranging from 0.05 to 1.0% w/w were employed to prepare functionalized PVA nanocomposites. The developed films exhibit adequate optical transparency, improved mechanical properties and extremely high antibacterial behavior due to the excellent dispersion of the functionalized CNTs into the PVA matrix.

  1. Poly(vinyl chloride) membrane alkali metal ion-selective electrodes based on crystalline synthetic zeolite of the Faujasite type

    International Nuclear Information System (INIS)

    Aghai, H.; Giahi, M.; Arvand Barmehi, M.

    2002-01-01

    Potentiometric electrodes based on the incorporation of zeolite particle in to poly (vinyl chloride) (pvc) membranes are described. The electrodes characteristics are evaluated regarding the response towards alkali ions. Pvc membranes plasticised with dibutyl phthalate and without lipophilic additives (co-exchanger) were used throughout this study. The electrode exhibits a Nernst ion response over the alkali metal cations concentration a range of 1.0x10 - 4 - 1.0 x 10 1 M with a slop of 57.0 ± 0.9 mV per decade of concentration a working ph range (3.0- 9.0) and a fast response time (≤15 c). The selective coefficients for cesium ion as test species with respect to alkaline earth, ammonium and some heavy metal ions were determined. Zeolite-PVC electrodes were applied to the determination of ionic surfactant

  2. Influence of Compounding Methods on Poly(vinyl) Alcohol/ Sago Pith Waste Bio composites: Mechanical and Water Absorption Properties

    International Nuclear Information System (INIS)

    Toh, W.Y.; Lai, J.C.; Aizan, W.A.R.W.

    2011-01-01

    Several methods of incorporating sago pith waste (SPW) into poly(vinyl alcohol) (PVA) had been conducted: (i) dry blending (PVA/SPW/G), (ii) blending of SPW and pre-plasticised PVA (pPVA/SPW/G) and (iii) blending of pre-plasticised of both PVA and SPW (pPVA/pSPW). The effect of the compounding method on the mechanical and water absorption properties were investigated. The addition of SPW into PVA greatly reduced the tensile strength and elongation at break. The tensile strength and elongation at break of PVA/SPW composites with identical geometry during compounding stage (powder/powder and pellet/pellet), which were PVA/SPW/G and pPVA/pSPW yielded the highest value. The percentage of water absorbed by PVA/SPW/G (without pre-plasticization) was the highest, followed by pPVA/pSPW and pPVA/SPW/G. (author)

  3. Comparison of Chain Conformation of Poly(vinyl alcohol) in Solutions and Melts from Quantum Chemistry Based Molecular Dynamics Simulations

    Science.gov (United States)

    Jaffe, Richard; Han, Jie; Matsuda, Tsunetoshi; Yoon, Do; Langhoff, Stephen R. (Technical Monitor)

    1997-01-01

    Confirmations of 2,4-dihydroxypentane (DHP), a model molecule for poly(vinyl alcohol), have been studied by quantum chemistry (QC) calculations and molecular dynamics (MD) simulations. QC calculations at the 6-311G MP2 level show the meso tt conformer to be lowest in energy followed by the racemic tg, due to intramolecular hydrogen bond between the hydroxy groups. The Dreiding force field has been modified to reproduce the QC conformer energies for DHP. MD simulations using this force field have been carried out for DHP molecules in the gas phase, melt, and CHCl3 and water solutions. Extensive intramolecular hydrogen bonding is observed for the gas phase and CHCl3 solution, but not for the melt or aqueous solution, Such a condensed phase effect due to intermolecular interactions results in a drastic change in chain conformations, in agreement with experiments.

  4. Synthesis of water-soluble poly [acrylic acid-co-vinyl butyl ether] and its applications in cement admixtures

    International Nuclear Information System (INIS)

    Negim, S.M.; Mun, G.A.; Nurkeeva, Z.S.; Danveesh, H.H.M.

    2005-01-01

    Three composition ratios of poly[acrylic acid (AA)-co-vinyl butyl ether)] were prepared in alcoholic solution using azo-bis-isobutyro-nitrile as initiator (ABIN). The water-soluble copolymers were characterized through FT-IR, 1 H NMR, Mass spectra, ESEM as well as viscosity. The effect of water-soluble copolymers and their sodium salts on the physico-mechanical properties of Ordaniary Portland Cement (O.P.C) pastes was investigated. The results showed that the addition of aqueous solutions from the prepared copolymers and their sodium salts to the cement improve most of the specific characteristics of (O.P.C). As the concentration of the water-soluble copolymer increases, the setting time increases. The combined water content enhances the addition of copolymer to the mixing water. The compressive strength was she increased at all any hydration. The results of the solution of the prepared sodium salt copolymers are better than its copolymers. (author)

  5. Thermal degradation and plasticizing mechanism of poly(vinyl chloride) plasticized with a novel cardanol derived plasticizer

    Science.gov (United States)

    Chen, J.; Nie, X. A.; Jiang, J. C.; Zhou, Y. H.

    2018-01-01

    A natural plasticizer cardanol derivatives glycidyl ether (CGE) was synthesized and employed as a plasticizer for the poly(vinyl chloride). The effect of CGE on thermal degradation of PVC films and its plasticizing mechanism were firstly reported. The molecular structure of CGE was characterized with Fourier transform infrared spectroscopy (FTIR). Thermal properties, degradation properties and compatibility of the PVC films were investigated by Differential scanning calorimeter analysis (DSC), Thermogravimetric analysis (TGA) and FTIR, respectively. Compared with the commercial plasticizers dioctylphthalate (DOP), CGE can endow PVC film with a decrease of 4.31 °C in glass transition temperature (Tg), an increase of 24.01 °C and 25.53 °C in 10% weight loss (T 10) and 50% weight loss (T 50) respectively, and a higher activetion energy of thermal degradation (Ea ).

  6. Structural analysis of poly(vinyl alcohol hydrogels) produced by freezing and thawing process Positron annihilation lifetime spectroscopy (PALS)

    International Nuclear Information System (INIS)

    Paranhos, Caio M.; Oliveira, Renata N.; Soares, Bluma G.

    2005-01-01

    In this work, poly(vinyl alcohol) hydrogels with a entrapped polyelectrolyte were characterized through Positron Annihilation Lifetime Spectroscopy (PALS). PALS was used to determine the average pore radii (R), average free volume (V f ) and the intensity of ortho-positronium (I 3 ). The free volume estimated for the hydrogels increases with increasing polyelectrolyte content, while the intensity of o-Ps decreases with the increasing polyelectrolyte content. Degree of crystallinity of the samples decreases with the presence of polyelectrolyte. The structural changes observed can be discussed in terms of the changes in hydrogels structure due to a hindrance capacity of the polyelectrolyte on the crystalline behavior and the different polymer-polymer interactions. (author)

  7. Neutron spin-echo studies on dynamic and static fluctuations in two types of poly(vinyl alcohol) gels

    International Nuclear Information System (INIS)

    Kanaya, T.; Takahashi, N.; Nishida, K.; Seto, H.; Nagao, M.; Takeda, T.

    2005-01-01

    We report neutron spin-echo measurements on two types of poly(vinyl alcohol) (PVA) gels. The first is PVA gel in a mixture of dimethyl sulfoxide (DMSO) and water with volume ratio 60/40, and the second is PVA gel in an aqueous borax solution. The observed normalized intermediate scattering functions I(Q,t)/I(Q,0) are very different between them. The former I(Q,t)/I(Q,0) shows a nondecaying component in addition to a fast decay, but the latter does not have the nondecaying one. This clearly indicates that the fluctuations in the former PVA gel consist of static and dynamic fluctuations whereas the latter PVA gel does include only the dynamic fluctuations. The dynamic fluctuations of the former and latter gels have been analyzed in terms of a restricted motion in the network and Zimm motion, respectively, and the origins of these motions will be discussed

  8. Effect of trap states and microstructure on charge carrier conduction mechanism through semicrystalline poly(vinyl alcohol) granular film

    Science.gov (United States)

    Das, A. K.; Bhowmik, R. N.; Meikap, A. K.

    2018-05-01

    We report a comprehensive study on hysteresis behaviour of current-voltage characteristic and impedance spectroscopy of granular semicrystalline poly(vinyl alcohol) (PVA) film. The charge carrier conduction mechanism and charge traps of granular PVA film by measuring and analyzing the temperature dependent current-voltage characteristic indicate a bi-stable electronic state in the film. A sharp transformation of charge carrier conduction mechanism from Poole-Frenkel emission to space charge limited current mechanism has been observed. An anomalous oscillatory behaviour of current has been observed due to electric pulse effect on the molecular chain of the polymer. Effect of microstructure on charge transport mechanism has been investigated from impedance spectroscopy analysis. An equivalent circuit model has been proposed to explain the result.

  9. Effect of hygroscopic materials on water vapor permeation and dehumidification performance of poly(vinyl alcohol) membranes

    KAUST Repository

    Bui, T. D.

    2017-01-16

    In this study, two hygroscopic materials, inorganic lithium chloride (LiCl) and organic triethylene glycol (TEG) were separately added to poly(vinyl alcohol) (PVA) to form blend membranes for air dehumidification. Water vapor permeation, dehumidification performance and long-term durability of the membranes were studied systematically. Membrane hydrophilicity and water vapor sorbability increased significantly with higher the hygroscopic material contents. Water vapor permeance of the membranes increased with both added hygroscopic material and absorbed water. Water permeation energy varied from positive to negative with higher hygroscopic content. This observation is attributed to a lower diffusion energy and a relatively constant sorption energy when hygroscopic content increases. Comparatively, PVA/TEG has less corrosive problems and is more environmentally friendly than PVA/LiCl. A membrane with PVA/TEG is observed to be highly durable and is suitable for dehumidification applications.

  10. Electro spinning of Poly(ethylene-co-vinyl alcohol) Nano fibres Encapsulated with Ag Nanoparticles for Skin Wound Healing

    International Nuclear Information System (INIS)

    Xu, Ch.; Wang, B.; Lu, T.; Xu, F.; Xu, F.; Wang, B.; Xu, F.

    2011-01-01

    Skin wound healing is an urgent problem in clinics and military activities. Although significant advances have been made in its treatment, there are several challenges associated with traditional methods, for example, limited donor skin tissue for transplantation and inflammation during long-term healing time. To address these challenges, in this study we present a method to fabricate Poly(ethylene-co-vinyl alcohol) (EVOH) nano fibres encapsulated with Ag nanoparticle using electro spinning technique. The fibres were fabricated with controlled diameters (59 nm 3μm) by regulating three main parameters, that is, EVOH solution concentration, the electric voltage, and the distance between the injection needle tip (high-voltage point) and the fibre collector. Ag was added to the nano fibres to offer long-term anti-inflammation effect by slow release of Ag nanoparticles through gradual degradation of EVOH nano fibre. The method developed here could lead to new dressing materials for treatment of skin wounds.

  11. Active film of poly(vinyl chloride)/silver: synthesis, characterization and evaluation as antimicrobial active packaging

    International Nuclear Information System (INIS)

    Braga, Lilian R.; Rangel, Ellen T.; Machado, Fabricio

    2015-01-01

    The antimicrobial films based on poly(vinyl chloride) (PVC) mediated silver (1, 2, 4 and 8 wt%) were evaluated as antimicrobial active packaging using the casting method. The structure of the active films was characterized by SEM, EDX-XRF, XRD, FTIR and TG. FTIR spectra confirmed the PVC-Ag interaction due to the presence of new bands at 1745 cm"-"1 and 1165 cm"-"1 bands, which are absent in the PVC control. The FRX-EDX spectrum confirmed the presence of silver ions in all the films. TG and SEM results showed that the increased concentration of silver provided an improved thermal stability and presence of pores in the active films, respectively. Antimicrobial activity was evaluated by disk diffusion method for Bacillus subtilis, Fusarium solani and Apergillus niger, which proved the efficiency of the films active. (author)

  12. Fatigue characterization of Poly Vinyl Chloride (PVC) foam core sandwich composite using the G-control method

    DEFF Research Database (Denmark)

    Manca, Marcello; Berggreen, Christian; Carlsson, Leif A.

    2016-01-01

    This paper presents experimental results from cyclic crack propagation tests performed on sandwich specimens with glass/epoxy face sheets and Poly Vinyl Chloride (PVC) foam cores using the G-controlled cyclic energy release rate (ΔG) test procedure. The face material was tested in tension......, compression and shear to determine in-plane and out-of-plane mechanical properties, such as Young’s modulus, Poisson’s ratio and shear modulus. These properties were then used in an analytical model of the mixed-mode bending sandwich specimen to calculate compliance and energy release rate. Finite element...... on tested specimens, highlighting the influence of mode mixity and foam density on the crack path. Crack propagation diagrams showing da/dN versus ΔG curves were obtained to establish the Paris-Erdogan relation for each material combination tested at the two mode-mixities. Results showed constant crack...

  13. Optical and morphological characterizations of pyronin dye-poly (vinyl alcohol) thin films formed on glass substrates

    International Nuclear Information System (INIS)

    Meral, Kadem; Arik, Mustafa; Onganer, Yavuz

    2016-01-01

    Thin films of pyronin dye mixed with poly(vinyl alcohol) (PVA) on glass substrate were prepared by using spin-coating technique. The optical and morphological properties of the thin films were studied by UV-Vis., steady-state fluorescence spectroscopies and atomic force microscopy (AFM). The thin films on glass substrate were fabricated at various [PVA]/[dye] (P/D) ratios. Hence, the monomeric and H-aggregates thin films of pyronin dye mixed with PVA were formed as a function of the dye and PVA concentration. It was determined that while the monomeric thin films showed strong fluorescence, the formation of H-aggregates in the thin film caused to decreasing the fluorescence intensity. AFM studies demonstrated that the morphology of the thin film was drastically varied with changing the optical property of the thin film such as monomeric and H-aggregates thin films.

  14. Optical and morphological characterizations of pyronin dye-poly (vinyl alcohol) thin films formed on glass substrates

    Energy Technology Data Exchange (ETDEWEB)

    Meral, Kadem, E-mail: kademm@atauni.edu.tr; Arik, Mustafa, E-mail: marik@tatauni.edu.tr; Onganer, Yavuz, E-mail: yonganer@atauni.edu.tr [Department of Chemistry, Faculty of Sciences, Atatürk University, 25240 Erzurum (Turkey)

    2016-04-18

    Thin films of pyronin dye mixed with poly(vinyl alcohol) (PVA) on glass substrate were prepared by using spin-coating technique. The optical and morphological properties of the thin films were studied by UV-Vis., steady-state fluorescence spectroscopies and atomic force microscopy (AFM). The thin films on glass substrate were fabricated at various [PVA]/[dye] (P/D) ratios. Hence, the monomeric and H-aggregates thin films of pyronin dye mixed with PVA were formed as a function of the dye and PVA concentration. It was determined that while the monomeric thin films showed strong fluorescence, the formation of H-aggregates in the thin film caused to decreasing the fluorescence intensity. AFM studies demonstrated that the morphology of the thin film was drastically varied with changing the optical property of the thin film such as monomeric and H-aggregates thin films.

  15. Influence of UV and Gamma radiations on the induced birefringence of stretched poly(vinyl) alcohol foils

    Science.gov (United States)

    Nechifor, Cristina-Delia; Zelinschi, Carmen Beatrice; Dorohoi, Dana-Ortansa

    2014-03-01

    The aim of our paper is to evidence the influence of Gamma and UV radiations on the induced birefringence of poly(vinyl alcohol) stretched foils. Thin foils of PVA were prepared and dried without modifying their surfaces. The polymeric foils were irradiated from 15 min to 6 h using UV and Gamma radiations. The induced by stretching under heating birefringence of PVA films was measured at λ = 589.3 nm with a Babinet Compensator. Physico-chemical processes (photo stabilization, photo degradation, oxidation) induced by irradiation of polymer matrix influence both the stretching degree and the anisotropy of etired foils. An increase of birefringence versus the stretching ratio of the PVA foils was evidenced for all studied samples. The dependence of the birefringence on the exposure time, stretching ratio and nature of radiation was also confirmed.

  16. Antibacterial and wound healing properties of chitosan/poly(vinyl alcohol)/zinc oxide beads (CS/PVA/ZnO).

    Science.gov (United States)

    Gutha, Yuvaraja; Pathak, Janak L; Zhang, Weijiang; Zhang, Yaping; Jiao, Xu

    2017-10-01

    Treatment against bacterial infection is crucial for wound healing. Development of cost-effective antibacterial agent with wound healing properties is still in high demand. In this study we aimed to design chitosan/poly(vinyl alcohol)/zinc oxide (CS/PVA/ZnO) beads as novel antibacterial agent with wound healing properties. CS/PVA/ZnO beads were synthesized, and characterized by using XRD, FTIR, SEM, and TEM analysis. Pure chitosan exhibits two peaks at 2θ=10 and 20 and the CS/PVA polymer matrix exhibit the peaks at 2θ=19.7° and another of low intensity at 2θ=11.5°. Pure ZnO shows the characteristic peaks at (100), (002), (101), (102), (110), (103), (200), and (112) that were in good agreement with wurtzite ore having hexagonal lattice structure. The antibacterial activity of CS/PVA/ZnO against Escherichia coli, and Staphylococcus aureus were evaluated with the zone of inhibition method. Antibacterial activity of CS/PVA/ZnO was higher than that of chitosan (CS) and poly(vinyl alcohol (PVA). Hemocompatibility and biocompatibility of CS/PVA/ZnO were tested in in vitro. Wound healing properties of CS/PVA/ZnO were tested in mice skin wound. CS/PVA/ZnO showed strong antimicrobial, wound healing effect, hemocompatibility and biocompatibility. Hence the results strongly support the possibility of using this novel CS/PVA/ZnO material for the anti bacterial and wound healing application. Copyright © 2017 Elsevier B.V. All rights reserved.

  17. Novel modified poly vinyl chloride blend membranes for removal of heavy metals from mixed ion feed sample

    Energy Technology Data Exchange (ETDEWEB)

    Nayak, Vignesh; Jyothi, M.S. [Centre for Nano and Material Sciences, Jain University, Jain Global Campus, Kanakapura Ramanagaram, Bangalore, 562112 (India); Balakrishna, R. Geetha, E-mail: br.geetha@jainuniversity.ac.in [Centre for Nano and Material Sciences, Jain University, Jain Global Campus, Kanakapura Ramanagaram, Bangalore, 562112 (India); Padaki, Mahesh, E-mail: sp.mahesh@jainuniversity.ac.in [Centre for Nano and Material Sciences, Jain University, Jain Global Campus, Kanakapura Ramanagaram, Bangalore, 562112 (India); National University of Science and Technology “MISIS”, Moscow, 119049 (Russian Federation); Deon, Sebastien [Institut UTINAM, UMR CNRS 6213, Université de Bourgogne-Franche-Comté,16 route de Gray, Besançon Cedex 25030 (France)

    2017-06-05

    Highlights: • Work reports the novel modification of poly vinyl chloride (PVC) using newly developed method. • Blend membranes were prepared using modified PVC and polysulfone in different compositions. • The prepared blend membranes were used for separation of different heavy metal ions. • The blend membranes showed improved rejection of heavy metal ions in comparison to Commercial NF 270 membrane. - Abstract: Herein, an attempt has been made to prepare a novel membrane with good efficiency for removal of heavy metal ions namely lead (Pb), cadmium (Cd) and chromium (Cr). 4-amino benzoic acid (ABA) was covalently grafted onto the poly vinyl chloride (PVC) backbone by C−N bond to enhance the hydrophilicity. {sup 1}H NMR and ATR-IR spectroscopy analysis confirmed the chemical modification of PVC. Further the modified polymer was blended in different compositions with polysulfone (PSf) for optimization. Morphological changes that occurred in blend membranes, due to the incorporation of modified PVC was studied by AFM and SEM techniques. The effect on hydrophilicity and performance of blends owing to incorporation of modified PVC was evaluated by water uptake, contact angle and flux studies. The density of functional groups in blends was analyzed by its ion-exchange capacity. Batch wise filtration of metal ions was carried out and the effect of pressure, feed pH and interference of ions was thoroughly investigated. Essentially, 100% rejection was obtained for all the metal ions in acidic pH with a productivity of 2.56 l/m{sup 2} h. The results were correlated with the results of commercially available NF 270 membrane under the same operating conditions.

  18. Macroporous poly(vinyl alcohol) microspheres bearing phosphate groups as a new adsorbent for low-density lipoprotein apheresis

    Energy Technology Data Exchange (ETDEWEB)

    Wang Weichao; Xie Hui; Ou Lailiang; Wang Lianyong; Yu Yaoting; Kong Deling [Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Science, Nankai University, Tianjin 300071 (China); Sun Lisha, E-mail: wly@nankai.edu.c, E-mail: kongdeling@nankai.edu.c [General Hospital, Tianjin Medical University, Tianjin 300052 (China)

    2009-12-15

    A new low-density lipoprotein (LDL) adsorbent with phosphate groups as the ligand was prepared in this study. Macroporous poly(vinyl acetate-co-triallyl isocyanurate) microspheres were prepared using a free-radical suspension polymerization method. A hydrolysis reaction in sodium hydroxide/methanol changed the materials into poly(vinyl alcohol) (PVA) microspheres. Further reaction with phosphorus oxychloride in anhydrous DMF led to the LDL adsorbent PVA-phosphate microspheres. The preparation conditions such as reaction time, temperature and the amount of phosphorus oxychloride were optimized. The adsorption of plasma lipoproteins was examined by in vitro adsorption assays. The influence of adsorption time, plasma volume and ionic strength on the adsorption capacity was investigated. The circulation adsorption showed that the pathogenic lipoproteins in the plasma such as total cholesterol (TC), LDL and triglyceride (TG) could be removed markedly, in which the removal percentages were 42.9%, 45.0% and 44.74%, respectively. However, the reduction of high-density lipoprotein (HDL) and other normal plasma components was very slight. For in vivo experiment, rabbits were fed with high-cholesterol food to develop a hyperlipidemia model and treated by extracorporeal blood perfusion using the PVA-phosphate columns. Eight hyperlipidemia rabbits were treated with the PVA-phosphate adsorbent, and the removal of TC, LDL and TG was 45.03 +- 6.64%, 48.97 +- 9.92% and 35.42 +- 14.17%, respectively. The sterilization and storage tests showed that the adsorbent was chemically and functionally stable. It could be easily sterilized by a common method and stored for months without loss of adsorption capacity. Therefore, this new PVA-phosphate-based LDL adsorbent may have potential for application in LDL apheresis.

  19. Macroporous poly(vinyl alcohol) microspheres bearing phosphate groups as a new adsorbent for low-density lipoprotein apheresis

    International Nuclear Information System (INIS)

    Wang Weichao; Xie Hui; Ou Lailiang; Wang Lianyong; Yu Yaoting; Kong Deling; Sun Lisha

    2009-01-01

    A new low-density lipoprotein (LDL) adsorbent with phosphate groups as the ligand was prepared in this study. Macroporous poly(vinyl acetate-co-triallyl isocyanurate) microspheres were prepared using a free-radical suspension polymerization method. A hydrolysis reaction in sodium hydroxide/methanol changed the materials into poly(vinyl alcohol) (PVA) microspheres. Further reaction with phosphorus oxychloride in anhydrous DMF led to the LDL adsorbent PVA-phosphate microspheres. The preparation conditions such as reaction time, temperature and the amount of phosphorus oxychloride were optimized. The adsorption of plasma lipoproteins was examined by in vitro adsorption assays. The influence of adsorption time, plasma volume and ionic strength on the adsorption capacity was investigated. The circulation adsorption showed that the pathogenic lipoproteins in the plasma such as total cholesterol (TC), LDL and triglyceride (TG) could be removed markedly, in which the removal percentages were 42.9%, 45.0% and 44.74%, respectively. However, the reduction of high-density lipoprotein (HDL) and other normal plasma components was very slight. For in vivo experiment, rabbits were fed with high-cholesterol food to develop a hyperlipidemia model and treated by extracorporeal blood perfusion using the PVA-phosphate columns. Eight hyperlipidemia rabbits were treated with the PVA-phosphate adsorbent, and the removal of TC, LDL and TG was 45.03 ± 6.64%, 48.97 ± 9.92% and 35.42 ± 14.17%, respectively. The sterilization and storage tests showed that the adsorbent was chemically and functionally stable. It could be easily sterilized by a common method and stored for months without loss of adsorption capacity. Therefore, this new PVA-phosphate-based LDL adsorbent may have potential for application in LDL apheresis.

  20. Novel modified poly vinyl chloride blend membranes for removal of heavy metals from mixed ion feed sample

    International Nuclear Information System (INIS)

    Nayak, Vignesh; Jyothi, M.S.; Balakrishna, R. Geetha; Padaki, Mahesh; Deon, Sebastien

    2017-01-01

    Highlights: • Work reports the novel modification of poly vinyl chloride (PVC) using newly developed method. • Blend membranes were prepared using modified PVC and polysulfone in different compositions. • The prepared blend membranes were used for separation of different heavy metal ions. • The blend membranes showed improved rejection of heavy metal ions in comparison to Commercial NF 270 membrane. - Abstract: Herein, an attempt has been made to prepare a novel membrane with good efficiency for removal of heavy metal ions namely lead (Pb), cadmium (Cd) and chromium (Cr). 4-amino benzoic acid (ABA) was covalently grafted onto the poly vinyl chloride (PVC) backbone by C−N bond to enhance the hydrophilicity. 1 H NMR and ATR-IR spectroscopy analysis confirmed the chemical modification of PVC. Further the modified polymer was blended in different compositions with polysulfone (PSf) for optimization. Morphological changes that occurred in blend membranes, due to the incorporation of modified PVC was studied by AFM and SEM techniques. The effect on hydrophilicity and performance of blends owing to incorporation of modified PVC was evaluated by water uptake, contact angle and flux studies. The density of functional groups in blends was analyzed by its ion-exchange capacity. Batch wise filtration of metal ions was carried out and the effect of pressure, feed pH and interference of ions was thoroughly investigated. Essentially, 100% rejection was obtained for all the metal ions in acidic pH with a productivity of 2.56 l/m 2 h. The results were correlated with the results of commercially available NF 270 membrane under the same operating conditions.

  1. Self-assembly behavior of poly(fluorenyl styrene)-block-poly(2-vinyl pyridine) and their blends with single wall carbon nanotubes (SWCNT)

    Science.gov (United States)

    Mezzenga, Raffaele; Li, Chaoxu; Hsu, Jung-Ching; Chen, Wen-Chang; Sugiyama, Kenji; Hirao, Akira

    2010-03-01

    We describe a supramolecular strategy to disperse carbon nanotubes in block copolymer matrices. To achieve the desired functions and morphologies, comb-type architectures in which one and two fluorene units attached on the styrene ring of polystyrene-block-poly(2-vinyl pyridine) were studied. Depending on the pendant fluorene units, the block ratio, the casting solvent and thermal annealing history, multiple morphologies were found. The phase diagram, compared to PS-b-P2VP, was interpreted in terms of the conformational asymmetry arising from grafting of fluorene units of variable lengths. Hydrogen bonds between COOH-SWCNT and P2VP favor miscibility of SWCNT within P2VP domains and the blending of these two components is reflected both on the final morphologies and on the electron conductivity of the blends.

  2. Effect of different plasticizers on poly(N-vinyl-2-pyrrolidone) hydrogels cross-linked by radiation

    International Nuclear Information System (INIS)

    Alcantara, Mara Tania S.; Giannini, Danielle R.; Brant, Antonio J.C.; Riella, Humberto G.; Lugao, Ademar B.

    2011-01-01

    The use of hydrogel membranes usually demands polymers capable of forming films with high elastic and flexible properties besides having high water absorption. In terms of improvements of polymer plasticity, addition of special plasticizers to polymers can do it with promising results, although within limits of concentrations. The objective of this study was to evaluate the different effects of poly(enthylene glycol) (PEG) and glycerol as plasticizers on hydrogel membranes synthesized from poly(N-vinyl-2-pyrrolidone) (PVP) as the main polymer in aqueous polymeric solutions. For that, hydrogels of PVP/agar/PEG, PVP/agar/glycerol and without agar or plasticizer were simultaneously synthesized and sterilized by irradiation of mixtures of such products in aqueous solutions, using gamma-rays from 60 Co source at a dose of 25 kGy. The results based on gel fraction, swelling in water, and some mechanical tests suggest that the degree of PVP cross-linking prevailed over the greater hydrophilicity of glycerol compared to that of PEG with regard to the degree of swelling of the hydrogels. (author)

  3. Preparation of nanogels by radiation-induced cross-linking of interpolymer complexes of poly (acrylic acid) with poly (vinyl pyrrolidone) in aqueous medium

    Science.gov (United States)

    Ghaffarlou, Mohammadreza; Sütekin, S. Duygu; Güven, Olgun

    2018-01-01

    Functional nanogels were prepared from interpolymer complexes (IPC) of poly (vinyl pyrrolidone) and poly (acrylic acid) by gamma irradiation of their aqueous solutions. The coil size of IPCs prepared under different experimental conditions (polymer molecular weight, concentration, mixing ratios, pH and temperature) were measured by Dynamic Light Scattering (DLS) technique prior to irradiation. At relatively low absorbed doses of 5 and 10 kGy, IPC nanogels with a range of 30-250 nm diameters, -12 to -28 mV zeta potentials and polydispersities lower than 0.17 were obtained. The sizes of the nanogels were found to be smaller than the size of the precursor IPC coil sizes (40-300 nm) due to the formation of intra-chain crosslinks. Thus a recipe of preparing multifunctional nanogels with double amphiphilic properties carrying polyacidic and nonionic polymer structures with the range of above listed properties has been developed. These nanogels show narrow size distribution and high colloidal stability increasing their potential to be used as biocompatible drug carriers with controlled-release properties. PVP-PAA IPC nanogels were characterized by dynamic light scattering (DLS), atomic force microscopy (AFM) and scanning electron microscopy (SEM) techniques.

  4. Topologically Micropatterned Collagen and Poly(ε-caprolactone) Struts Fabricated Using the Poly(vinyl alcohol) Fibrillation/Leaching Process To Develop Efficiently Engineered Skeletal Muscle Tissue.

    Science.gov (United States)

    Kim, Minseong; Kim, WonJin; Kim, GeunHyung

    2017-12-20

    Optimally designed three-dimensional (3D) biomedical scaffolds for skeletal muscle tissue regeneration pose significant research challenges. Currently, most studies on scaffolds focus on the two-dimensional (2D) surface structures that are patterned in the micro-/nanoscales with various repeating sizes and shapes to induce the alignment of myoblasts and myotube formation. The 2D patterned surface clearly provides effective analytical results of pattern size and shape of the myoblast alignment and differentiation. However, it is inconvenient in terms of the direct application for clinical usage due to the limited thickness and 3D shapeability. Hence, the present study suggests an innovative hydrogel or synthetic structure that consists of uniaxially surface-patterned cylindrical struts for skeleton muscle regeneration. The alignment of the pattern on the hydrogel (collagen) and poly(ε-caprolactone) struts was attained with the fibrillation of poly(vinyl alcohol) and the leaching process. Various cell culture results indicate that the C2C12 cells on the micropatterned collagen structure were fully aligned, and that a significantly high level of myotube formation was achieved when compared to the collagen structures that were not treated with the micropatterning process.

  5. Sulfonated poly(ether ether ketone)/poly(vinyl alcohol) sensitizing system for solution photogeneration of small Ag, Au, and Cu crystallites.

    Science.gov (United States)

    Korchev, A S; Shulyak, T S; Slaten, B L; Gale, W F; Mills, G

    2005-04-28

    Illumination of air-free aqueous solutions containing sulfonated poly(ether ether ketone) and poly(vinyl alcohol) with 350 nm light results in benzophenone ketyl radicals of the polyketone. The polymer radicals form with a quantum yield 0.02 and decay with a second-order rate constant 6 orders of magnitude lower than that of typical alpha-hydroxy radicals. Evidence is presented that the polymeric benzophenone ketyl radicals reduce Ag+, Cu2+, and AuCl4- to metal particles of nanometer dimensions. Decreases in the reduction rates with increasing Ag(I), Cu(II), and Au(III) concentrations are explained using a kinetic model in which the metal ions quench the excited state of the polymeric benzophenone groups, which forms the macromolecular radicals. Quenching is fastest for Ag+, whereas Cu2+ and AuCl4- exhibit similar rate constants. Particle formation becomes more complex as the number of equivalents needed to reduce the metal ions increases; the Au(III) system is an extreme case where the radical reactions operate in parallel with secondary light-initiated and thermal reduction channels. For each metal ion, the polymer-initiated photoreactions produce crystallites possessing distinct properties, such as a very strong plasmon in the Ag case or the narrow size distribution exhibited by Au particles.

  6. Preparation, characterization, and application of poly(vinyl alcohol)-graft-poly(ethylene glycol) resins: novel polymer matrices for solid-phase synthesis.

    Science.gov (United States)

    Luo, Juntao; Pardin, Christophe; Zhu, X X; Lubell, William D

    2007-01-01

    Spherical crosslinked poly(vinyl alcohol) (PVA) beads with good mechanical stability were prepared by reverse-suspension polymerization, using dimethyl sulfoxide (DMSO) as a cosolvent in an aqueous phase. Poly(ethylene glycol)s with varying chain lengths were grafted onto the PVA beads by anionic polymerization of ethylene oxide. The thermal behavior, morphology, and swelling were evaluated for each of the new polymer matrices. High loading and good swelling in water and organic solvents were characteristic of the PEG-grafted PVA beads. The polymer beads also exhibited good mechanical and chemical stability and were unaffected by treatment with 6 N HCl and with 6 N NaOH. The hydroxyl groups of the PVA-PEG beads were converted into aldehyde, carboxylic acid, and isocyanate functions to provide scavenger resins and were extended by way of a benzyl alcohol in a Wang linker. The transglutaminase substrates dipeptides (Z-Gln-Gly) and heptapeptides (Pro-Asn-Pro-Gln-Leu-Pro-Phe) were synthesized on PVA-PEG_5, PVA-PEG_20, and the Wang linker-derivatized PVA-PEG resins. The cleavage of the peptides from the resins using MeOH/NH3 mixture at different temperatures (0 degrees C and room temp) and 50% TFA/DCM provided, respectively, peptide methyl esters, amides, and acids in good yields and purity as assessed by LC-MS analysis.

  7. Preparation of a microporous polymer electrolyte based on poly(vinyl chloride)/poly(acrylonitrile-butyl acrylate) blend for Li-ion batteries

    International Nuclear Information System (INIS)

    Tian, Zheng; Pu, Weihua; He, Xiangming; Wan, Chunrong; Jiang, Changyin

    2007-01-01

    Poly(acrylonitrile-co-butyl acrylate) (P(AN-co-BuA))/poly(vinyl chloride) (PVC) blend-based gel polymer electrolyte (BGPE) was prepared for lithium-ion batteries. The P(AN-co-BuA)/PVC BGPE consists of an electrolyte-rich phase, which is mainly composed of P(AN-co-BuA) and liquid electrolyte, acting as a conducting channel and a PVC-rich phase that provides mechanical strength. The dual phase was just simply developed by the difference of miscibility properties in solvent, PC, between P(AN-co-BuA) and PVC. The mechanical strength of this new blend electrolyte was found to be much higher, with a fracture stress as high as 29 MPa in dry membrane and 21 MPa in gel state, than that of a previously reported P(AN-co-BuA)-based gel polymer electrolyte. The blended gel polymer electrolyte showed ionic conductivity of higher than 1.5 x 10 -3 S cm -1 and electrochemical stability up to at least 4.8 V. The results showed that the as-prepared gel polymer electrolytes were promising materials for lithium-ion batteries

  8. Preparation of a microporous polymer electrolyte based on poly(vinyl chloride)/poly(acrylonitrile-butyl acrylate) blend for Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Tian, Zheng; Pu, Weihua; He, Xiangming; Wan, Chunrong; Jiang, Changyin [Institute of Nuclear and New Energy Technology, Tsinghua University, Beijing 100084 (China)

    2007-02-15

    Poly(acrylonitrile-co-butyl acrylate) (P(AN-co-BuA))/poly(vinyl chloride) (PVC) blend-based gel polymer electrolyte (BGPE) was prepared for lithium-ion batteries. The P(AN-co-BuA)/PVC BGPE consists of an electrolyte-rich phase, which is mainly composed of P(AN-co-BuA) and liquid electrolyte, acting as a conducting channel and a PVC-rich phase that provides mechanical strength. The dual phase was just simply developed by the difference of miscibility properties in solvent, PC, between P(AN-co-BuA) and PVC. The mechanical strength of this new blend electrolyte was found to be much higher, with a fracture stress as high as 29 MPa in dry membrane and 21 MPa in gel state, than that of a previously reported P(AN-co-BuA)-based gel polymer electrolyte. The blended gel polymer electrolyte showed ionic conductivity of higher than 1.5 x 10{sup -3} S cm{sup -1} and electrochemical stability up to at least 4.8 V. The results showed that the as-prepared gel polymer electrolytes were promising materials for lithium-ion batteries. (author)

  9. Flexible and strong ternary blends of poly(vinyl chloride), poly(butylene adipate)and nanoparticle-plasticizers

    OpenAIRE

    Yin, Bo; Hakkarainen, Minna

    2013-01-01

    Multiple property enhancement was achieved for ternary blends of PVC, poly(butylene adipate) (PBA) plasticizer and PBA-grafted nanofillers as compared to ternary blends with untreated nanofillers. The blends with surface modified halloysite, kaolin or silicon dioxide nanofillers all exhibited higher stress at break and higher strain at break as compared to the corresponding composites with untreated nanoparticles. The strain at break was similar or improved compared to binary PVC/PBA blends. ...

  10. Temperature Dependent Electrical Transport in Al/Poly(4-vinyl phenol/p-GaAs Metal-Oxide-Semiconductor by Sol-Gel Spin Coating Method

    Directory of Open Access Journals (Sweden)

    Şadan Özden

    2016-01-01

    Full Text Available Deposition of poly(4-vinyl phenol insulator layer is carried out by applying the spin coating technique onto p-type GaAs substrate so as to create Al/poly(4-vinyl phenol/p-GaAs metal-oxide-semiconductor (MOS structure. Temperature was set to 80–320 K while the current-voltage (I-V characteristics of the structure were examined in the study. Ideality factor (n and barrier height (ϕb values found in the experiment ranged from 3.13 and 0.616 eV (320 K to 11.56 and 0.147 eV (80 K. Comparing the thermionic field emission theory and thermionic emission theory, the temperature dependent ideality factor behavior displayed that thermionic field emission theory is more valid than the latter. The calculated tunneling energy was 96 meV.

  11. Field and laboratory determination of a poly(vinyl/vinylidene chloride) additive in brick mortar.

    Science.gov (United States)

    Law, S L; Newman, J H; Ptak, F L

    1990-02-01

    A polymerized vinyl/vinylidene chloride additive, used in brick mortar during the 60s and 70s, is detected at the building site by the field method, which employs a commercially available chloride test strip. The field test results can then be verified by the laboratory methods. In one method, total chlorine in the mortar is determined by an oxygen-bomb method and the additive chloride is determined by difference after water-soluble chlorides have been determined on a separate sample. In the second method, the polymerized additive is extracted directly from the mortar with tetrahydrofuran (THF). The difference in weight before and after extraction of the additive gives the weight of additive in the mortar. Evaporation of the THF from the extract leaves a thin film of the polymer, which gives an infrared "fingerprint" spectrum characteristic of the additive polymer.

  12. Replacement of Poly(vinyl pyrrolidone) by Thiols: A Systematic Study of Ag Nanocube Functionalization by Surface-Enhanced Raman Scattering

    OpenAIRE

    Moran, Christine H.; Rycenga, Matthew; Zhang, Qiang; Xia, Younan

    2011-01-01

    In this work, we used surface-enhanced Raman scattering (SERS) to monitor the replacement of poly(vinyl pyrrolidone) (PVP) on Ag nanocubes by cysteamine, thiol-terminated PEG, and benzenedithiol. PVP is widely used as a colloidal stabilizer and capping agent to control the shape of Ag (as well as many other noble metals) nanocrystals during synthesis, and to stabilize the final colloidal suspension. However, the surface chemistry of Ag nanocrystals often needs to be tailored for specific appl...

  13. NMR study of temperature-induced phase separation and polymer-solvent interactions in poly(vinyl methyl ether)/D.sub.2./sub.O/ethanol solutions

    Czech Academy of Sciences Publication Activity Database

    Hanyková, L.; Labuta, J.; Spěváček, Jiří

    2006-01-01

    Roč. 47, č. 17 (2006), s. 6107-6116 ISSN 0032-3861 Grant - others:GA UK 294/2004/B Institutional research plan: CEZ:AV0Z40500505 Keywords : poly(vinyl methyl ether)/D2O/ ethanol solutions * temperature-induced phase separation * 1H and 13C NMR spectroscopy Subject RIV: CD - Macromolecular Chemistry Impact factor: 2.773, year: 2006

  14. Preparation and properties of poly(vinyl alcohol)-g-octadecanol copolymers based solid–solid phase change materials

    International Nuclear Information System (INIS)

    Shi Haifeng; Li Jianhua; Jin Yanmei; Yin Yiping; Zhang Xingxiang

    2011-01-01

    Highlights: ► In this paper, our objective is just focused on the preparation and characterization of such SSPCMs aiming at providing one suitable material for improving the thermal stability and preventing the liquid leakage from the matrix. Here, the SSPCMs can be fabricated by grafting to method between poly(vinyl alcohol) and octadecanol, which the grafting ratio can be controlled by adjusting the feeding components. ► The thermal properties, crystalline structure and morphology were detailed studies by WAXD, FT-IR, TGA and DSC, proving that the PVA-g-octadecanol process the better thermal storage ability and thermal stability. Compared with pure octadecanol, the heat fusion of PVA-g-octadecanol decreased due to the mobility confinement and the lower rearrangements of C18 alkyl side chains. ► This result is for the first time reported, and is a meaningful result for the investigation of the solid–solid phase change materials, and the preparation process provides one template-directed approach to obtain the high-performance materials with the better heat storage and thermal stability. - Abstract: The heat storage and phase transition behavior of a series of poly(vinyl alcohol)-g-octadecanol copolymers (PVA-g-C18OH) with apparent grafting ratios ranging from 283 to 503%, synthesized through “grafting to” method, has been investigated by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), wide-angle X-ray diffraction (WAXD) and polarized optical microscopy (POM). PVA-g-C18OH copolymers exhibit the better thermal stability against C18OH, and the thermal energy storage ability (ΔH m ) is of dependence on the apparent grafting ratios. Compared with C18OH, the lower thermal storage efficiency possible is attributed to the less CH 2 groups entered into the crystalline domains and the frustrated mobility of the grafted C18 alkyl side chains between PVA backbones. The results show that

  15. The improvement of polyethylene prostheses through radiation crosslinking

    International Nuclear Information System (INIS)

    Du Plessis, T.A.; Grobbelaar, C.J.; Marais, F.

    1977-01-01

    During the past decade, remarkable progress has been made in the utilization of high-density polyethylene (HDPE) as a material for the manufacture of prostheses used in orthopaedic operations. This polymer contributes largely to the success of total hip replacement. In the case of total knee replacement it was considered imperative that a more hard-wearing polymer should be developed if at all possible, because not only are the cold-flow characteristics of ordinary high-density polyethylene at high pressures a limiting factor, but particle formation from friction can furthermore lead to physiological side-effects which adversely affect the efficacy of joints made from this material, especially so in the case of knee-joints. Bearing in mind the excellent improvements to be obtained through the radiation crosslinking of polyethylene film, the radiation crosslinking of high-density polyethylene prostheses seemed to be a logical avenue to investigate. Experimental details are presented. Gamma radiation was used. Impact strength and tensile strength measurements were made on specimens irradiated over a dose range of 0 to 80 Mrad. The results are discussed. (U.K.)

  16. Mechanical and electromagnetic interference shielding Properties of poly(vinyl alcohol)/graphene and poly(vinyl alcohol)/multi-walled carbon nanotube composite nanofiber mats and the effect of Cu top-layer coating.

    Science.gov (United States)

    Fujimori, Kazushige; Gopiraman, Mayakrishnan; Kim, Han-Ki; Kim, Byoung-Suhk; Kim, Ick-Soo

    2013-03-01

    We report the mechanical property and electromagnetic interference shielding effectiveness (EMI SE) of poly(vinyl alcohol) (PVA)/graphene and PVA/multi-walled carbon nanotube (MWCNT) composite nanofibers prepared by electrospinning. The metal (Cu) was deposited on the resultant PVA composite nanofibers using metal deposition technique in order to improve the mechanical properties and EMI shielding properties. The resulting PVA composite nanofibers and Cu-deposited corresponding nanofibers were characterized by field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and wide angle X-ray diffraction (WAXD). Tensile tests were performed on the PVA/graphene and PVA/MWCNT composite nanofibers. The tensile strength of the PVA/graphene and PVA/MWCNT composite nanofibers was found to be 19.2 +/- 0.3 MPa at graphene content - 6.0 wt% and 12.2 +/- 0.2 MPa at MWCNT content - 3.0 wt%, respectively. The EMI SE of the Cu-deposited PVA/graphene composite nanofibers was significantly improved compared to pure PVA/graphene composite nanofibers, and also depended on the thickness of Cu metal layer deposited on the PVA composite nanofibers.

  17. Radiation Synthesis of Poly(N-Vinyl Pyrrolidone) Nanogels and Nanoscale Grafting of Poly(Acrylic Acid) from Cellulose

    International Nuclear Information System (INIS)

    Guven, Olgun; Isik, Semiha Duygu; Barsbay, Murat

    2010-01-01

    Ionizing radiation has long been known to be a very useful tool for the preparation of nanogels. Although preparation is straightforward, the control of the sizes of nanogels has been a challenging issue. This report shows the results of our work on using radiation for the synthesis of PVP nanogels in the range of 40-200nm by making use of the principles of solution thermodynamics of aqueous polymer solutions. Nanoscale grafting of responsive polymers however has been of scientific and industrial importance due to fine control of the molecular weight and molecular weight distribution of grafted polymers. The second part of this report deals with the grafting of poly(acrylic acid) onto the surface of cellulose, thus imparting pH response to the substrate. The use of radiation as a constant source of radical generation and Reversible-Addition-Fragmentation-Chain transfer agents for the control of free radical polymerization provided a full control over the molecular weight and distribution of poly(acrylic acid) grafts on cellulose. (author)

  18. Radiation Synthesis of Poly(N-Vinyl Pyrrolidone) Nanogels and Nanoscale Grafting of Poly(Acrylic Acid) from Cellulose

    Energy Technology Data Exchange (ETDEWEB)

    Guven, Olgun; Isik, Semiha Duygu; Barsbay, Murat [Hacettepe University, Department of Chemistry, 06800 Ankara (Turkey)

    2010-07-01

    Ionizing radiation has long been known to be a very useful tool for the preparation of nanogels. Although preparation is straightforward, the control of the sizes of nanogels has been a challenging issue. This report shows the results of our work on using radiation for the synthesis of PVP nanogels in the range of 40-200nm by making use of the principles of solution thermodynamics of aqueous polymer solutions. Nanoscale grafting of responsive polymers however has been of scientific and industrial importance due to fine control of the molecular weight and molecular weight distribution of grafted polymers. The second part of this report deals with the grafting of poly(acrylic acid) onto the surface of cellulose, thus imparting pH response to the substrate. The use of radiation as a constant source of radical generation and Reversible-Addition-Fragmentation-Chain transfer agents for the control of free radical polymerization provided a full control over the molecular weight and distribution of poly(acrylic acid) grafts on cellulose. (author)

  19. Synthesis of Poly(N-vinyl-2-pyrrolidone-co-methyl methacrylate by Maghnite-H+ a Non-toxic Catalyst

    Directory of Open Access Journals (Sweden)

    Mohamed Benadda

    2014-10-01

    Full Text Available In the present work poly (N-vinyl-2-pyrrolidone-co-methyl methacrylate copolymers were prepared successfully and cleanly by a one step process via cationic copolymerization of N-vinyl-2-pyrrolidone (NVP with methyl methacrylate (MMA, in heterogeneous phase using “Maghnite-H+” (Mag-H+ as catalyst in bulk, Maghnite is a montmorillonite sheet silicate clay exchanged with protons to produce Maghnite-H+. Temperature is varied between 20 and 80 °C. The effects of reaction temperature, amount of Mag-H+ on the yield and the intrinsic viscosity (η were investigated. A typical reaction product of poly (NVP-co- MMA was analyzed by infra red spectroscopy (FTIR and 1H-NMR, 13C-NMR spectroscopy as well as by viscosimetry. © 2014 BCREC UNDIP. All rights reservedReceived: 24th November 2013; Revised: 30th June 2014; Accepted: 8th July 2014How to Cite: Benadda, M., Ferrahi, M.I., Belbachir, M. (2014. Synthesis of Poly(N-vinyl-2-pyrrolidone-co-methyl methacrylate by Maghnite-H+ a Non-toxic Catalyst. Bulletin of Chemical Reaction Engineering & Catalysis, 9 (3: 201-206. (doi: 10.9767/bcrec.9.3.5743.201-206Permalink/DOI: http://dx.doi.org/10.9767/bcrec.9.3.5743.201-206

  20. Preparation of robust braid-reinforced poly(vinyl chloride) ultrafiltration hollow fiber membrane with antifouling surface and application to filtration of activated sludge solution.

    Science.gov (United States)

    Zhou, Zhuang; Rajabzadeh, Saeid; Fang, Lifeng; Miyoshi, Taro; Kakihana, Yuriko; Matsuyama, Hideto

    2017-08-01

    Braid-reinforced hollow fiber membranes with high mechanical properties and considerable antifouling surface were prepared by blending poly(vinyl chloride) (PVC) with poly(vinyl chloride-co-poly(ethylene glycol) methyl ether methacrylate) (poly(VC-co-PEGMA)) copolymer via non-solvent induced phase separation (NIPS). The tensile strength of the braid-reinforced PVC hollow fiber membranes were significantly larger than those of previously reported various types of PVC hollow fiber membranes. The high interfacial bonding strength indicated the good compatibility between the coating materials and the surface of polyethylene terephthalate (PET)-braid. Owing to the surface segregation phenomena, the membrane surface PEGMA coverage increased upon increasing the poly(VC-co-PEGMA)/PVC blending ratio, resulting in higher hydrophilicities and bovine serum albumin (BSA) repulsion. To compare the fouling properties, membranes with similar PWPs were prepared by adjusting the dope solution composition to eliminate the effect of hydrodynamic conditions on the membrane fouling performance. The blend membranes surface exhibited considerable fouling resistance to the molecular adsorption from both BSA solution and activated sludge solution. In both cases, the flux recovered to almost 80% of the initial flux using only water backflush. Considering their great mechanical properties and antifouling resistance to activated sludge solution, these novel membranes show good potential for application in wastewater treatment. Copyright © 2017 Elsevier B.V. All rights reserved.

  1. Preparation and characterization of novel solid polymer blend electrolytes based on poly (vinyl pyrrolidone) with various concentrations of lithium perchlorate

    Energy Technology Data Exchange (ETDEWEB)

    Kesavan, K., E-mail: kesavanphysics@gmail.com [School of Physics, Alagappa University, Karaikudi 630003, Tamilnadu (India); Mathew, Chithra M. [School of Physics, Alagappa University, Karaikudi 630003, Tamilnadu (India); Rajendran, S., E-mail: sraj54@yahoo.com [School of Physics, Alagappa University, Karaikudi 630003, Tamilnadu (India); Ulaganathan, M. [Energy Research Institute @ NTU, Nanyang Technological University, Singapore 637 553 (Singapore)

    2014-05-01

    Graphical abstract: - Highlights: • The maximum ionic conductivity value was found to be 0.2307 × 10{sup −5} S cm{sup −1} for PEO(90 wt%)/PVP(10 wt%)/LiClO{sub 4}(8 wt%) based electrolyte at room temperature. • The structural and functional groups were studied by XRD and FTIR. • Both direct and indirect optical band gap values were evaluated from UV–vis analysis. • The change in viscosity of the polymer electrolytes was studied by photoluminescence spectra. - Abstract: A series of conducting novel solid polymer blend electrolytes (SPE) based on the fixed ratio of poly (ethylene oxide)/poly (vinyl pyrrolidone) (PEO/PVP) and various concentrations of salt lithium perchlorate (LiClO{sub 4}) were prepared by solvent casting technique. Structural and complex formation of the prepared electrolytes was confirmed by X-ray diffraction and FTIR analyses. The maximum ionic conductivity value was found to be 0.2307 × 10{sup −5} S cm{sup −1} for 8 wt% of LiClO{sub 4} based system at ambient temperature. Thermal stability of the present system was studied by thermo gravimetric/differential thermal analysis (TG/DTA). Surface morphology of the sample having maximum ionic conductivity was studied by atomic force microscope (AFM). Optical properties like direct and indirect band gaps were investigated by UV–vis analysis. The change in viscosity of the polymer complexes were also identified using photoluminescence emission spectra. PEO(90)/PVP(10)/LiClO{sub 4}(8) has the highest conductivity which is supported by the lowest optical band gap and lowest intensity in photoluminescence spectroscopy near 400–450 nm.

  2. Influence of gamma irradiation dose and concentration of laponite clay on Poly (N-Vinyl-2-Pyrrolidone) hydrogels

    International Nuclear Information System (INIS)

    Santos, Vinicius J.; Zafalon, Angélica T.; Lugão, Ademar B.; Parra, Duclerc F.

    2017-01-01

    Hydrogels are polymeric biomaterials widely used in biomedicine and defined as an insoluble system of one or more crosslinked hydrophilic polymers, capable of absorbing large amounts of fluids without losing their physical integrity. Composed by one three-dimensional network of crosslinked polymer chains they can be synthesized by various physical and chemical methods including radiation. One of these methods is the gamma irradiation process, which forms the crosslinked network and sterilizes the material in a single step. In the biomedical field one of hydrogels applications is the transdermal dressings, these systems have an impact of great value in the treatment of wounds, as they can protect regions injured by burns, cuts and even chronic wounds. The association of clay to hydrogels promotes a modification of properties of these materials, such as swelling and gel fraction. Thus, the objective of this work was to evaluate the swelling properties and gel fraction of hydrogels based on polymer formulation of poly (N-vinyl-2-pyrrolidone), poly (ethylene glycol), agar containing nano-clay laponite RD in Different concentrations (0, 0.01, 0.1, 0.5, 1, 2, 5, 10, 20%). The materials were mixed by stirring and heating and then processed by gamma radiation from Co-60 at doses of 10, 25, 50 and 70 kGy. To evaluate the gel fraction, the membranes were immersed in water for 3 weeks. The swelling was evaluated after 48 hours of immersion in distilled water at room temperature. It was observed that as the clay concentration increases regardless of the irradiation dose the amount of gel fraction decreased and the amount of water absorption increased. (author)

  3. Influence of gamma irradiation dose and concentration of laponite clay on Poly (N-Vinyl-2-Pyrrolidone) hydrogels

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Vinicius J.; Zafalon, Angélica T.; Lugão, Ademar B.; Parra, Duclerc F., E-mail: vinicius.jusan@gmail.com [Instituto de Pesquisas Energéticas e Nucleares (IPEN/CNEN-SP), São Paulo, SP (Brazil)

    2017-07-01

    Hydrogels are polymeric biomaterials widely used in biomedicine and defined as an insoluble system of one or more crosslinked hydrophilic polymers, capable of absorbing large amounts of fluids without losing their physical integrity. Composed by one three-dimensional network of crosslinked polymer chains they can be synthesized by various physical and chemical methods including radiation. One of these methods is the gamma irradiation process, which forms the crosslinked network and sterilizes the material in a single step. In the biomedical field one of hydrogels applications is the transdermal dressings, these systems have an impact of great value in the treatment of wounds, as they can protect regions injured by burns, cuts and even chronic wounds. The association of clay to hydrogels promotes a modification of properties of these materials, such as swelling and gel fraction. Thus, the objective of this work was to evaluate the swelling properties and gel fraction of hydrogels based on polymer formulation of poly (N-vinyl-2-pyrrolidone), poly (ethylene glycol), agar containing nano-clay laponite RD in Different concentrations (0, 0.01, 0.1, 0.5, 1, 2, 5, 10, 20%). The materials were mixed by stirring and heating and then processed by gamma radiation from Co-60 at doses of 10, 25, 50 and 70 kGy. To evaluate the gel fraction, the membranes were immersed in water for 3 weeks. The swelling was evaluated after 48 hours of immersion in distilled water at room temperature. It was observed that as the clay concentration increases regardless of the irradiation dose the amount of gel fraction decreased and the amount of water absorption increased. (author)

  4. Mechanical and interfacial properties of poly(vinyl chloride) based composites reinforced by cassava stillage residue with different surface treatments

    Science.gov (United States)

    Zhang, Yanjuan; Gan, Tao; Li, Qian; Su, Jianmei; Lin, Ye; Wei, Yongzuo; Huang, Zuqiang; Yang, Mei

    2014-09-01

    Cassava stillage residue (CSR), a kind of agro-industrial plant fiber, was modified by coupling agent (CA), mechanical activation (MA), and MA-assisted CA (MACA) surface treatments, respectively. The untreated and different surface treated CSRs were used to prepare plant fibers/polymer composites (PFPC) with poly(vinyl chloride) (PVC) as polymer matrix, and the properties of these CSR/PVC composites were compared. Surface treated CSR/PVC composites possessed better mechanical properties, water resistance and dimensional stability compared with the untreated CSR/PVC composite, attributing to the improvement of interfacial properties between CSR and PVC matrix. MACA-treated CSR was the best reinforcement among four types of CSRs (untreated, MA-treated, CA-treated, and MACA-treated CSRs) because MACA treatment led to the significant improvement of dispersion, interfacial adhesion and compatibility between CSR and PVC. MACA treatment could be considered as an effective and green method for enhancing reinforcement efficiency of plant fibers and the properties of PFPC.

  5. Efficient in situ synthetic routes of polyaniline/poly(vinyl alcohol)/TiO2 nanocomposites using gamma irradiation

    Science.gov (United States)

    Afify, T. A.; Ghazy, O. A.; Saleh, H. H.; Ali, Z. I.

    2018-02-01

    Gamma radiation was used to prepare nanocomposites based on polyaniline/titanium dioxide (PANI/TiO2) or polyaniline/poly (vinyl alcohol)/titanium dioxide (PANI/PVA/TiO2). It was found that PANI/TiO2 in the form of nanocomposite as shown by the UV/vis spectroscopy. This was through the appearance and shift of two absorption peaks at 340 and 598 nm. The SEM micrographs of the PANI/TiO2 nanocomposites showed a fibrous morphology before the treatment with HCl. The TiO2 nanoparticles are clearly seen to be precipitated on the PANI fibers and the morphology changed towards the sheets shape with highly distribution on PANI surface. The transmission electron microscopy (TEM) image confirms the fibrous shape of the PANI and spherical shape of TiO2 nanoparticles. The XRD study showed a several diffraction patterns of TiO2 nanoparticles confirming the PANI/TiO2 and PANI/PVA/TiO2 nanocomposites. The FT-IR analysis indicated that there is an interfacial interaction existed between the PANI and its inorganic counterpart of TiO2 nanoparticles. The dielectric constant of the PANI/PVA showed the lowest values and was increased by either doping with TiO2 or increasing irradiation dose.

  6. Poly(vinyl alcohol) films reinforced with nanofibrillated cellulose (NFC) isolated from corn husk by high intensity ultrasonication.

    Science.gov (United States)

    Xiao, Shaoliang; Gao, Runan; Gao, LiKun; Li, Jian

    2016-01-20

    This work was aimed at fabricating and characterizing poly(vinyl alcohol) films that were reinforced by nanofibrillated corn husk celluloses using a combination of chemical pretreatments and ultrasonication. The obtained nanofibrillated celluloses (NFCs) possessed a narrow width ranging from 50 to 250 nm and a high aspect ratio (394). The crystalline type of NFC was cellulose I type. Compared with the original corn husks, the NCF crystallinity and thermal stability increased due to the removal of the hemicelluloses and lignin. PVA films containing different NFC concentrations (0.5%, 1%, 3%, 5%, 7% and 9%, w/w, dry basis) were examined. The 1% PVA/NFC reinforced films exhibited a highly visible light transmittance of 80%, and its tensile strength and the tensile strain at break were increased by 1.47 and 1.80 times compared to that of the pure PVA film, respectively. The NFC with high aspect ratio and high crystallinity is beneficial to the improvement of the mechanical strength and thermal stability. Copyright © 2015 Elsevier Ltd. All rights reserved.

  7. Intelligent poly (vinyl alcohol)-chitosan nanoparticles-mulberry extracts films capable of monitoring pH variations.

    Science.gov (United States)

    Ma, Qianyun; Liang, Tieqiang; Cao, Lele; Wang, Lijuan

    2018-03-01

    The aim of this study was to prepare a visually responsive intelligent film based on poly (vinyl alcohol) (PVA), chitosan nanoparticles (CHNPs) and mulberry extracts (MBE). CHNPs were first prepared by using ionotropic gelation method to enhance the mechanical properties of PVA based films. The morphology, particle size, zeta potential and crystallinity of CHNPs were measured. The resultant CHNPs were spherical with a diameter of 381.2nm, with high stability and a zeta potential of 49.1±1.33mV. The film with 6% CHNPs (P-C6) had the highest tensile strength (∼73.43MPa). MBE was incorporated into the P-C6 film. The film containing 20% MBE had the highest tensile strength and showed visible color responses to variations across pH 1-13. The film was tested by monitoring the spoilage of fish. The color of the film changed from red to green as the fish spoiled. Therefore, the pH responsive intelligent film developed here can be used as a package label to detect food spoilage. Copyright © 2017 Elsevier B.V. All rights reserved.

  8. Self-supported poly(methyl methacrylate-acrylonitrile-vinyl acetate)-based gel electrolyte for lithium ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Liao, Y.H.; Zhou, D.Y.; Rao, M.M.; Cai, Z.P.; Liang, Y. [School of Chemistry and Environment, South China Normal University, Guangzhou 510006 (China); Li, W.S.; Tan, C.L. [School of Chemistry and Environment, South China Normal University, Guangzhou 510006 (China); Key Lab of Electrochemical Technology on Energy Storage and Power Generation in Guangdong Universities, Guangzhou 510006 (China)

    2009-04-01

    Self-supported gel polymer electrolyte (GPE) was prepared based on copolymer, poly(methyl methacrylate-acrylonitrile-vinyl acetate) (P(MMA-AN-VAc)). The copolymer P(MMA-AN-VAc) was synthesized by emulsion polymerization and the copolymer membrane was prepared through phase inversion. The structure and the performance of the copolymer, the membrane and the GPE were characterized by FTIR, NMR, SEM, XRD, DSC/TG, LSV, CA, and EIS. It is found that the copolymer was formed through the breaking of double bond C=C in each monomer. The membrane has low crystallinity and has low glass transition temperature, 39.1 C, its thermal stability is as high as 310 C, and its mechanical strength is improved compared with P(MMA-AN). The GPE is electrochemically stable up to 5.6 V (vs. Li/Li{sup +}) and its conductivity is 3.48 x 10{sup -3} S cm{sup -1} at ambient temperature. The lithium ion transference number in the GPE is 0.51 and the conductivity model of the GPE is found to obey the Vogel-Tamman-Fulcher (VTF) equation. (author)

  9. A study on poly (N-vinyl-2-pyrrolidone covalently bonded NiTi surface for inhibiting protein adsorption

    Directory of Open Access Journals (Sweden)

    Hongyan Yu

    2016-12-01

    Full Text Available Near equiatomic NiTi alloys have been extensively applied as biomaterials owing to its unique shape memory effect, superelasticity and biocompatibility. It has been demonstrated that surfaces capable of preventing plasma protein adsorption could reduce the reactivity of biomaterials with human blood. This motivated a lot of researches on the surface modification of NiTi alloy. In the present work, following heat and alkaline treatment and silanization by trichlorovinylsilane (TCVS, coating of poly (N-vinyl-2-pyrrolidone (PVP was produced on the NiTi alloy by gamma ray induced chemical bonding. The structures and properties of modified NiTi were characterized and in vitro biocompatibility of plasma protein adsorption was investigated. The results indicated that heat treatment at 823 K for 1 h could result in the formation of a protective TiO2 layer with “Ni-free” zone on NiTi surface. It was found that PVP was covalently bonded on NiTi surface to create a hydrophilic layer for inhibiting protein adsorption on the surface. The present work offers a green approach to introduce a bioorganic surface on metal and other polymeric or inorganic substrates by gamma irradiation.

  10. Influence of the covalent immobilization of graphene oxide in poly(vinyl alcohol) on human osteoblast response.

    Science.gov (United States)

    Linares, Javier; Matesanz, María Concepción; Feito, María José; Salavagione, Horacio Javier; Martínez, Gerardo; Gómez-Fatou, Marián; Portolés, María Teresa

    2016-02-01

    The differences in the response of human Saos-2 osteoblasts to nanocomposites of poly(vinyl alcohol) (PVA) and 1.5wt.% graphene oxide (GO) prepared by covalent linking (PVA/GO-c) and simple blending (PVA/GO-m) have been evaluated through different biocompatibility parameters. The effects produced on osteoblasts by these two nanocomposites were analysed in parallel and compared with the direct action of GO and with the effect of PVA films without GO. The intracellular content of reactive oxygen species (ROS) and the levels of interleukin-6 (IL-6) were measured to evaluate oxidative stress induction and protective response, respectively. The results demonstrate that the combination of GO with PVA reduces both the proliferation delay and the internal cell complexity alterations induced by GO on human osteoblasts. Moreover, the covalent attachment of GO to the PVA chains increases both cell viability and IL-6 levels, reducing both apoptosis and intracellular ROS content when compared to simple blending of both materials. The use of this strategy to modulate the biointerface reduces the toxic effects of graphene while preserving the reinforcement characteristics for application in tissue engineering scaffolds, and has enormous interest for polymer/graphene biomaterials development. Copyright © 2015 Elsevier B.V. All rights reserved.

  11. Structure, corrosion behavior and mechanical property of a novel poly(vinyl alcohol) composite in simulated body fluid.

    Science.gov (United States)

    Li, Juan; Suo, Jinping; Zou, Peng; Jia, Lintao; Wang, Shifang

    2010-01-01

    The data for long-term drug-delivery systems are scarce compared to the short-term systems because the required research efforts are more time-consuming. In this study, we report a novel cross-linked composite based on poly(vinyl alcohol) (PVA) containing cupric ions for long-term delivery, which is helpful for contraception and trace element balance in the human body. The composition, corrosion products, crystal structure, chemical structure and mechanical stability of the composite, after being immersed in simulated body fluid (SBF) for one year, were studied by X-ray fluorescence spectroscopy (XRF), X-ray diffraction (XRD), differential scanning calorimetry (DSC), Fourier-transform infrared spectroscopy (FT-IR) and mechanical testing. The results show that no other new elements, such as P, Cl and Ca, appear on the surface of the composite and no Cu(2)O was formed after immersion in SBF for one year. The effectiveness of copper can be greatly improved and the side-effects caused by these compounds might also be eliminated. Furthermore, this novel composite exhibits long-term mechanical stability in SBF. The present in vitro long-term data suggest that this novel copper-containing composite may serve as a substitute for conventional materials of copper-containing intrauterine devices (Cu-IUDs) and as a carrier for controlled-release material in a variety of other applications.

  12. Sugar-Responsive Layer-by-Layer Film Composed of Phenylboronic Acid-Appended Insulin and Poly(vinyl alcohol).

    Science.gov (United States)

    Takei, Chihiro; Ohno, Yui; Seki, Tomohiro; Miki, Ryotaro; Seki, Toshinobu; Egawa, Yuya

    2018-01-01

    Previous studies have shown that reversible chemical bond formation between phenylboronic acid (PBA) and 1,3-diol can be utilized as the driving force for the preparation of layer-by-layer (LbL) films. The LbL films composed of a PBA-appended polymer and poly(vinyl alcohol) (PVA) disintegrated in the presence of sugar. This type of LbL films has been recognized as a promising approach for sugar-responsive drug release systems, but an issue preventing the practical application of LbL films is combining them with insulin. In this report, we have proposed a solution for this issue by using PBA-appended insulin as a component of the LbL film. We prepared two kinds of PBA-appended insulin derivatives and confirmed that they retained their hypoglycemic activity. The LbL films composed of PBA-appended insulin and PVA were successfully prepared through reversible chemical bond formation between the boronic acid moiety and the 1,3-diol of PVA. The LbL film disintegrated upon treatment with sugars. Based on the results presented herein, we discuss the suitability of the PBA moiety with respect to hypoglycemic activity, binding ability, and selectivity for D-glucose.

  13. A novel crosslinking strategy for preparing poly(vinyl alcohol)-based proton-conducting membranes with high sulfonation

    Energy Technology Data Exchange (ETDEWEB)

    Tsai, Chun-En [Nanoelectrochemistry Laboratory, Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 106 (China); Lin, Chi-Wen [Department of Chemical Engineering, National Yunlin University of Science and Technology, Yunlin (China); Hwang, Bing-Joe [Nanoelectrochemistry Laboratory, Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 106 (China); National Synchrotron Radiation Research Center, Hsinchu 300 (China)

    2010-04-15

    This study synthesizes poly(vinyl alcohol) (PVA)-based polymer electrolyte membranes by a two-step crosslinking process involving esterization and acetal ring formation reactions. This work also uses sulfosuccinic acid (SSA) as the first crosslinking agent to form an inter-crosslinked structure and a promoting sulfonating agent. Glutaraldehyde (GA) as the second crosslinking agent, reacts with the spare OH group of PVA and forms, not only a dense structure at the outer membrane surface, but also a hydrophobic protective layer. Compared with membranes prepared by a traditional one-step crosslinking process, membranes prepared by the two-step crosslinking process exhibit excellent dissolution resistance in water. The membranes become water-insoluble even at a molar ratio of SO{sub 3}H/PVA-OH as high as 0.45. Moreover, the synthesized membranes also exhibit high proton conductivities and high methanol permeability resistance. The current study measures highest proton conductivity of 5.3 x 10{sup -2} S cm{sup -1} at room temperature from one of the synthesized membranes, higher than that of the Nafion {sup registered} membrane. Methanol permeability of the synthesized membranes measures about 1 x 10{sup -7} cm{sup 2} S{sup -1}, about one order of magnitude lower than that of the Nafion {sup registered} membrane. (author)

  14. Acai oil development and evaluation of immobilization and release in poly (N-vinyl-2-pyrrolidone) hydrogels

    International Nuclear Information System (INIS)

    Machado, Ana Carolina Henriques Ribeiro

    2010-01-01

    Acai (Euterpe oleracea) is a native palm of Brazil, distributed for the entire Amazonian basin. Rich in essentials fatty acids (mainly oleic acid and linoleic acid), acai oil prevents abnormal conditions of the skin, as dermatitis and drying, and assists in the regeneration of the epidermis. The benefits of the hydrogels are known as dressings. The purpose of this study was to develop devices for controlled release of acai oil on poly (N-vinyl-2-pyrrolidone) (PVP) hydrogels. The behavior of the acai oil front to the radiation was evaluated by the composition of fatty acids of the oil before and after irradiation. Two different matrices of PVP hydrogel were evaluated physically and chemically through assays of swelling, gel fraction, mechanical proprieties and in vitro cytotoxicity. Both matrices were considered adjusted to be used as an active release system. The devices were obtained by acai oil immobilization in PVP hydrogel matrices, were also characterized through assays of sweeling, gel fraction, mechanical proprieties and in vitro cytotoxicity. Moreover, they were characterized by assays of scanning electron microscopy and in vivo primary cutaneous irritation. Both devices were submitted to assay of active release kinetics, and the acai oil was quantified by gas chromatography coupled with mass spectrometry. The devices showed to be satisfactory to compose a release system of actives. (author)

  15. Poly (Vinyl Chloride Based Ion Selective Electrode for Determination of Zr (IV Ions Based on 2, 6-Dibenzylidenecyclohexanone

    Directory of Open Access Journals (Sweden)

    Syed A. Nabi

    2008-08-01

    Full Text Available A selective poly (vinyl chloride-based membrane sensor using 2,6-Dibenzylidenecyclohexanone as an ionophore have been prepared and explored as Zr (IV selective electrode. The sensitivity, working range and response time shows a significant dependence on the concentration of ionophore. The electrode prepared with 100 mg of PVC, 10 mg of ionophore and 5 ml of dibutylthylate shows the best performance. The electrode works well in the concentration range of 1×10-1-5×10-5 with a nerstian slope 55±2 eV and response time of 18 seconds. The sensor works well over the pH range 3-6. The sensor can be used for the period of over 1 month with out deviation in response characteristics. The selectivity of the electrode was studied and it was found that the electrode exhibited good selectivity for zirconium (IV over some alkaline earth metal ions. The electrode was also used as indicator electrode for potentiometeric titration of Zr (IV ions against EDTA solution.

  16. Graft copolymerization of N-vinyl-2-pyrrolidone onto pre-irradiated poly(vinylidene fluoride) powder

    International Nuclear Information System (INIS)

    Xu Chenqi; Huang Wei; Zhou Yongfeng; Yan Deyue; Chen Shutao; Huang Hua

    2012-01-01

    Graft copolymerization of N-vinyl-2-pyrrolidone (NVP) onto 60 Co γ-ray pre-irradiated poly (vinylidene fluoride) (PVDF) powder was investigated to find out the relationship between the degree of grafting (DG) and various factors, including monomer concentration, irradiation dose, reaction time, catalyst and so on. The DG can be calculated by comparing the amount of nitrogen element in the resulting copolymer (PVDF-g-PVP) powder with that in PVP on the basis of element analysis. The presence of PVP in the resulting PVDF powder was confirmed by the comparative studies of pristine PVDF and grafted PVDF powder through Fourier transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR), X-ray photoelectron spectroscopy (XPS), thermo gravimetric analyzer (TGA) and differential scanning calorimetry (DSC), respectively. When the reaction was performed at the monomer concentration of 20% (vol.) and the absorbed dose of 40 kGy for 3 h in water, the max. DG of 17.7% was obtained. - Highlights: ► We modify pristine PVDF powders with NVP by the pre-irradiated graft polymerization. ► The various factors influencing the degree of grafting are investigated in detail. ► The optimal condition of graft polymerization is obtained. ► The polymerization is processed at 20% (vol.) of NVP and 40kGy for 3 hours in water. ► The maximum degree of grafting is 17.7 % at such a condition.

  17. Morphological Study of Chitosan/Poly (Vinyl Alcohol Nanofibers Prepared by Electrospinning, Collected on Reticulated Vitreous Carbon

    Directory of Open Access Journals (Sweden)

    Diana Isela Sanchez-Alvarado

    2018-06-01

    Full Text Available In this work, chitosan (CS/poly (vinyl alcohol (PVA nanofibers were prepared by using the electrospinning method. Different CS concentrations (0.5, 1, 2, and 3 wt %, maintaining the PVA concentration at 8 wt %, were tested. Likewise, the studied electrospinning experimental parameters were: syringe/collector distance, solution flow and voltage. Subsequently, the electrospun fibers were collected on a reticulated vitreous carbon (RVC support for 0.25, 0.5, 1, 1.5, and 2 h. The morphology and diameter of the CS/PVA nanofibers were characterized by scanning electron microscopy (SEM, finding diameters in the order of 132 and 212 nm; the best results (uniform fibers were obtained from the solution with 2 wt % of chitosan and a voltage, distance, and flow rate of 16 kV, 20 cm, and 0.13 mL/h, respectively. Afterwards, a treatment with an ethanolic NaOH solution was performed, observing a change in the fiber morphology and a diameter decrease (117 ± 9 nm.

  18. Composite films based on biorelated agro-industrial waste and poly(vinyl alcohol). Preparation and mechanical properties characterization.

    Science.gov (United States)

    Chiellini, E; Cinelli, P; Imam, S H; Mao, L

    2001-01-01

    As a part of an ongoing project on the production of composite materials based on poly(vinyl alcohol) (PVA) and polymeric materials from renewable resources, the present paper reports on the incorporation of agricultural waste materials as organic fillers in a film matrix based on PVA as continuous phase. In this study lignocellulosic fibers byproducts, derived from sugar cane (SC) and apple (AP) and orange (OR) fruit juice extraction, were cast from PVA aqueous solutions. The effect of fiber type and composition on the relative properties of cast films was evaluated and compared. OR resulted to be suitable for blending in higher amounts by weight than SC and AP. Glycerol and urea were added as plasticizing agents and were observed to be effective in giving flexible films. Additionally, cornstarch was added to further increase the composition of polymers from renewable resources in cost-effective and ecoefficient composite film formulations. The prepared films resulted sensitive to moisture and water. To reduce water sensitivity, hexamethoxymethylmelamine (HMMM) was tested as a cross-linking agent for the present composite formulations. Cross-linked films exhibited significant improvement in water-resistance that can be taken as a tuneable structural feature for customized applications. The mechanical properties of the prepared composite films (elongation at break, tensile strength, Young modulus) were found to be dependent upon the nature and content of the filler and on environmental conditions.

  19. Enhanced mechanical, thermal and antimicrobial properties of poly(vinyl alcohol)/graphene oxide/starch/silver nanocomposites films.

    Science.gov (United States)

    Usman, Adil; Hussain, Zakir; Riaz, Asim; Khan, Ahmad Nawaz

    2016-11-20

    In the present work, synthesis of poly(vinyl alcohol)/graphene oxide/starch/silver (PVA/GO/Starch/Ag) nanocomposites films is reported. Such films have been characterized and investigated for their mechanical, thermal and antimicrobial properties. The exfoliation of GO in the PVA matrix occurs owing to the non-covalent interactions of the polymer chains of PVA and hydrophilic surface of the GO layers. Presence of GO in PVA and PVA/starch blends were found to enhance the tensile strength of the nanocomposites system. It was found that the thermal stability of PVA as well as PVA/starch blend systems increased by the incorporation of GO where strong physical bonding between GO layers and PVA/starch blends is assumed to cause thermal barrier effects. Antimicrobial properties of the prepared films were investigated against Escherichia coli and Staphylococcus aureus. Our results show enhanced antimicrobial properties of the prepared films where PVA-GO, PVA-Ag, PVA-GO-Ag and PVA-GO-Ag-Starch showed antimicrobial activity in ascending order. Copyright © 2016 Elsevier Ltd. All rights reserved.

  20. Preparation of Poly(Vinyl Alcohol) Grafted With Acrylic Acid/Styrene Binary Monomers For Selective Permeation of Heavy Metals

    International Nuclear Information System (INIS)

    Hegazy El-Sayed, A.; Abd El-Rehim, H.A.; Ali, A.M.; Aly, H.F.

    1999-01-01

    A study has been made to modify water-soluble poly(vinyl alcohol) (PVA), by grafting acrylic acid and styrene (AAc/Sty) binary monomers using gamma rays as initiator. The factors that affect the preparation process and grafting yield were studied and more economical grafts under the most favorable reaction conditions were obtained. It was found that the high degree of grafting of such system was obtained in presence of ethanol-water mixture in which water plays a significant role in enhancing the graft copolymerization. The critical amount of water to afford maximum grafting yield has been evaluated. The effect of comonomer composition on the grafting yield was also investigated and it was observed that using a mixture of AAc/Sty monomers influence the extent of grafting of each monomer onto the PVA substrate and the phenomenon of synergism occurs during such reaction. Also, degree of grafting increases as the content of the solvent decreases in the reaction medium. The permeation of heavy metals such as Ni and Co through the grafted membranes was investigated and efficiency of separation process is also determined

  1. Poly(vinyl Alcohol) Borate Gel Polymer Electrolytes Prepared by Electrodeposition and Their Application in Electrochemical Supercapacitors.

    Science.gov (United States)

    Jiang, Mengjin; Zhu, Jiadeng; Chen, Chen; Lu, Yao; Ge, Yeqian; Zhang, Xiangwu

    2016-02-10

    Gel polymer electrolytes (GPEs) have been studied for preparing flexible and compact electrochemical energy storage devices. However, the preparation and use of GPEs are complex, and most GPEs prepared through traditional methods do not have good wettability with the electrodes, which retard them from achieving their performance potential. In this study, these problems are addressed by conceiving and implementing a simple, but effective, method of electrodepositing poly(vinyl alcohol) potassium borate (PVAPB) GPEs directly onto the surfaces of active carbon electrodes for electrochemical supercapacitors. PVAPB GPEs serve as both the electrolyte and the separator in the assembled supercapacitors, and their scale and shape are determined solely by the geometry of the electrodes. PVAPB GPEs have good bonding to the active electrode materials, leading to excellent and stable electrochemical performance of the supercapacitors. The electrochemical performance of PVAPB GPEs and supercapacitors can be manipulated simply by adjusting the concentration of KCl salt used during the electrodeposition process. With a 0.9 M KCl concentration, the as-prepared supercapacitors deliver a specific capacitance of 65.9 F g(-1) at a current density of 0.1 A g(-1) and retain more than 95% capacitance after 2000 charge/discharge cycles at a current density of 1 A g(-1). These supercapacitors also exhibit intelligent high voltage self-protection function due to the electrolysis-induced cross-linking effect of PVAPB GPEs.

  2. Photochromic and thermal properties of poly(vinyl alcohol)/H6P2W18O62 hybrid membranes

    International Nuclear Information System (INIS)

    Gong Jian; Li Xiangdan; Shao Changlu; Ding Bin; Lee, Douk-Rae; Kim, Hak-Yong

    2003-01-01

    Poly(vinyl alcohol) (PVA) films, which contained different content of heteropolyacid (HPA) with Dawson-Wells structure, were prepared. The photochromic behavior was investigated by using ultraviolet-visible (UV-Vis) absorption spectroscopy. The result indicated that the film was reduced photochemically to yield a blue species under UV irradiation, and the color of the film changed to deep blue with increasing irradiation time and HPA content. The photochromic sensibility of different UV wavelength was investigated. In the UV-Vis spectra of the irradiated films, an isobestic point was observed at about 352 nm. The reduction mechanism of the heteropolyanion (W 6+ →W 5+ ) was suggested. The thermal property and the conductivity of the film were also studied. The thermal degradation step and the melting point of the film were influenced by different content of the HPA. Notably, the conductivity of 8.33x10 -6 S cm -1 was observed when the HPA content was 80 wt.%

  3. A novel approach for fabricating highly tunable and fluffy bioinspired 3D poly(vinyl alcohol) (PVA) fiber scaffolds.

    Science.gov (United States)

    Roy, Sunanda; Kuddannaya, Shreyas; Das, Tanya; Lee, Heng Yeong; Lim, Jacob; Hu, Xiao 'Matthew'; Chee Yoon, Yue; Kim, Jaehwan

    2017-06-01

    The excellent biocompatibility, biodegradability and chemo-thermal stability of poly(vinyl alcohol) (PVA) have been harnessed in diverse practical applications. These properties have motivated the fabrication of high performance PVA based nanofibers with adequate control over the micro and nano-architectures and surface chemical interactions. However, the high water solubility and hydrophilicity of the PVA polymer limits the application of the electrospun PVA nanofibers in aqueous environments owing to instantaneous dissolution. In this work, we report a novel yet facile concept for fabricating extremely light, fluffy, insoluble and stable three dimensional (3D) PVA fibrous scaffolds with/without coating for multifunctional purposes. While the solubility, morphology, fiber density and mechanical properties of nanofibers could be tuned by optimizing the cross-linking conditions, the surface chemical reactivity could be readily enhanced by coating with a polydopamine (pDA) bioinspired polymer without compromising the stability and innate properties of the native PVA fiber. The 3D pDA-PVA scaffolds exhibited super dye adsorption and constructive synergistic cell-material interactions by promoting healthy adhesion and viability of the human mesenchymal stem cells (hMSCs) within 3D micro-niches. We foresee the application of tunable PVA 3D as a highly adsorbent material and a scaffold material for tissue regeneration and drug delivery with close consideration of realistic in vivo parameters.

  4. Effect of Electron Beam Irradiation on the Structural Properties of Poly (Vinyl Alcohol) Formulations with Triphenyl Tetrazolium Chloride Dye (TTC)

    International Nuclear Information System (INIS)

    Ali, Z.I.; Said, H.M.; Ali, H.E.

    2005-01-01

    Films of poly (vinyl alcohol) (PVA) composites with triphenyl tetrazolium chloride (TTC) dye were prepared and exposed to various radiation doses delivered by accelerated electrons. The results showed that at a low dose of 50 kGy, the color difference (Δ E) of PVA/TTC films was increased by -10 times of the initial value. However, the change in colour differences did not go systematically with increasing the TTC content, in which the composite with 1.5 wt% displayed higher value than that with 3.5 wt%. The differential scanning calorimetry (DSC) showed that the presence of the TTC dye caused a depression in the melting point (Tm) and heat of fusion (Δ Hf) of the PVA bulk polymer. However, the thermogravimetric analysis (TGA) showed that the presence of the TTC dye improved the thermal stability of PVA. Also, the tensile strength at break of PVA/TTC composites was improved after electron beam irradiation. Keywords: PVA, PVA/TTC composites, Electron beam irradiation, color strength, FTIR, thermal and mechanical characterization

  5. Three-Dimensional Printed Poly(vinyl alcohol) Substrate with Controlled On-Demand Degradation for Transient Electronics.

    Science.gov (United States)

    Yoon, Jinsu; Han, Jungmin; Choi, Bongsik; Lee, Yongwoo; Kim, Yeamin; Park, Jinhee; Lim, Meehyun; Kang, Min-Ho; Kim, Dae Hwan; Kim, Dong Myong; Kim, Sungho; Choi, Sung-Jin

    2018-05-25

    Electronics that degrade after stable operation for a desired operating time, called transient electronics, are of great interest in many fields, including biomedical implants, secure memory devices, and environmental sensors. Thus, the development of transient materials is critical for the advancement of transient electronics and their applications. However, previous reports have mostly relied on achieving transience in aqueous solutions, where the transience time is largely predetermined based on the materials initially selected at the beginning of the fabrication. Therefore, accurate control of the transience time is difficult, thereby limiting their application. In this work, we demonstrate transient electronics based on a water-soluble poly(vinyl alcohol) (PVA) substrate on which carbon nanotube (CNT)-based field-effect transistors were fabricated. We regulated the structural parameters of the PVA substrate using a three-dimensional (3D) printer to accurately control and program the transience time of the PVA substrate in water. The 3D printing technology can produce complex objects directly, thus enabling the efficient fabrication of a transient substrate with a prescribed and controlled transience time. In addition, the 3D printer was used to develop a facile method for the selective and partial destruction of electronics.

  6. A Novel Research on Behavior of Zinc Ferrite Nanoparticles in Different Concentration of Poly(vinyl pyrrolidone (PVP

    Directory of Open Access Journals (Sweden)

    Halimah Mohamed Kamari

    2014-04-01

    Full Text Available Zinc ferrite nanocrystals were prepared from an aqueous solution containing metal nitrates and various of concentrations of poly(vinyl pyrrolidone (PVP, i.e., 0, 15, 40, and 55 g/L, as a capping agent. To stabilize the particles, they were thermally treated at 873 K, as an optimum calcination temperature. The behaviors of the polymeric precursor were analyzed by use of simultaneous thermo-gravimetry (TG and derivative thermo-gravimetry analyses (DTG. The presence of the crystalline phase in each sample was confirmed by X-ray diffraction (XRD analysis. The average particle size and the morphology of the nanoparticles were determined by transmission electron microscopy (TEM, and these parameters were found to differ at various concentrations of PVP. Fourier transform infrared spectroscopy (FT-IR confirmed the presence of metal oxide bands for all the PVP concentrations and confirmed the absence of organic bands for PVP concentrations less than 55 g/L. Measurements of the magnetization value of the zinc ferrite nanoparticles were obtained at room temperature by using a vibrating sample magnetometer (VSM, which showed that, in the absence of PVP, the sample exhibited a paramagnetic behavior while, in the presence of PVP, samples have a super-paramagnetic behavior.

  7. Effect of phosphorous-containing modified poly(vinyl alcohol on the mechanical and flame retardant properties of polypropylene

    Directory of Open Access Journals (Sweden)

    S. Sauca

    2015-04-01

    Full Text Available Blends of polypropylene (PP and different phosphorous-modified poly(vinyl alcohol (PVA derivatives synthesized on purpose, were prepared by both solvent and melt mixing, and fully characterized. Thermogravimetric analysis showed that the addition of the phosphorous-modified PVAs significantly increased thermal stability and charring of PP, probably due to their dehydration and the subsequent formation of a protective layer onto PP. SEM analysis demonstrated poor phase compatibility between PP and the polymeric additives, however acceptable dispersion of the polymeric additives was obtained. It was also observed that grafting of the modified PVA on PP occurred due to radical reactions arising during melt processing. Mechanical characterization showed that the elastic behavior of the blends was not altered with respect to neat PP, while ductility was reduced; on the other hand, impact resistance was considerably improved by blending. Slightly higher LOI values were obtained for the blends even with phosphorous content as small as 1 wt%; reduced dripping was also observed during the burning tests for the blend samples. Moreover, cone calorimeter test results showed that heat release rate, total heat release, and fire growth rate decreased compared with PP, in particular for the blends containing residual –OH groups on the PVA backbone. Therefore, these blends can find application where the combination of toughness and fire retardancy is required, such as in the automotive industry.

  8. Effect of Palm Oil Bio-Based Plasticizer on the Morphological, Thermal and Mechanical Properties of Poly(Vinyl Chloride

    Directory of Open Access Journals (Sweden)

    Kar Min Lim

    2015-10-01

    Full Text Available Flexible poly(vinyl chloride (PVC was fabricated using a palm oil-based alkyd as a co-plasticizer to di-octyl phthalate (DOP and di-isononyl phthalate (DiNP. The effects of the incorporation of the palm oil-based alkyd on morphological, thermal and mechanical properties of PVC compounds were studied. Results showed the incorporation of the alkyd enhanced the mechanical and thermal properties of the PVC compounds. Fourier transform infrared spectroscopy (FTIR results showed that the polar –OH and –C=O groups of alkyd have good interaction with the –C–Cl group in PVC via polar interaction. The morphological results showed good incorporation of the plasticizers with PVC. Improved tensile strength, elastic modulus, and elongation at break were observed with increasing amount of the alkyd, presumably due to chain entanglement of the alkyd with the PVC molecules. Thermogravimetric analysis results confirmed that the alkyd has improved the thermostability of the PVC compounds.

  9. Poly(vinyl alcohol) separators improve the coulombic efficiency of activated carbon cathodes in microbial fuel cells

    KAUST Repository

    Chen, Guang

    2013-09-01

    High-performance microbial fuel cell (MFC) air cathodes were constructed using a combination of inexpensive materials for the oxygen reduction cathode catalyst and the electrode separator. A poly(vinyl alcohol) (PVA)-based electrode separator enabled high coulombic efficiencies (CEs) in MFCs with activated carbon (AC) cathodes without significantly decreasing power output. MFCs with AC cathodes and PVA separators had CEs (43%-89%) about twice those of AC cathodes lacking a separator (17%-55%) or cathodes made with platinum supported on carbon catalyst (Pt/C) and carbon cloth (CE of 20%-50%). Similar maximum power densities were observed for AC-cathode MFCs with (840 ± 42 mW/m2) or without (860 ± 10 mW/m2) the PVA separator after 18 cycles (36 days). Compared to MFCs with Pt-based cathodes, the cost of the AC-based cathodes with PVA separators was substantially reduced. These results demonstrated that AC-based cathodes with PVA separators are an inexpensive alternative to expensive Pt-based cathodes for construction of larger-scale MFC reactors. © 2013 Elsevier B.V. All rights reserved.

  10. Development, characterization and biocompatibility of chondroitin sulfate/poly(vinyl alcohol)/bovine bone powder porous biocomposite.

    Science.gov (United States)

    da Silva, Gabriela T; Voss, Guilherme T; Kaplum, Vanessa; Nakamura, Celso V; Wilhelm, Ethel A; Luchese, Cristiane; Fajardo, André R

    2017-03-01

    Chondroitin sulfate (ChS), a sulfated glycosaminoglycan, poly(vinyl alcohol) (PVA) and bovine bone powder (BBP) were blended to form a novel eco-friendly biocomposite through cyclic freeze-thawing under mild conditions. The systematic investigation reveals that the content of BBP has a remarkable effect on the pore size, porosity, mechanical and liquid uptake properties and biodegradability. At 10wt.% BBP the biocomposite exhibited enhanced mechanical properties and biodegradability rate as compared to the pristine sample. Further, different properties of the biocomposite can be tailored according to the content of BBP. In vitro assays showed that ChS/PVA-BBP does not exert cytotoxicity against healthy cells. In vivo and ex vivo experiments revealed that ChS/PVA-BBP biocomposites are biocompatibility materials without exert pro-inflammatory responses. The biocomposite was completely biodegraded and bioresorbed after 15days of treatment. Taken together, BBP is a low-cost source of hydroxyapatite and collagen, which are insurance. All these results suggest that the biocomposite designed in this study is a promising biomaterial for potential skin tissue engineering. Copyright © 2016 Elsevier B.V. All rights reserved.

  11. Shape Memory Composites Based on Electrospun Poly(vinyl alcohol) Fibers and a Thermoplastic Polyether Block Amide Elastomer.

    Science.gov (United States)

    Shirole, Anuja; Sapkota, Janak; Foster, E Johan; Weder, Christoph

    2016-03-01

    The present study aimed at developing new thermally responsive shape-memory composites, that were fabricated by compacting mats of electrospun poly(vinyl alcohol) (PVA) fibers and sheets of a thermoplastic polyether block amide elastomer (PEBA). This design was based on the expectation that the combination of the rubber elasticity of the PEBA matrix and the mechanical switching exploitable through the reversible glass transition temperature (Tg) of the PVA filler could be combined to create materials that display shape memory characteristics as an emergent effect. Dynamic mechanical analyses (DMA) show that, upon introduction of 10-20% w/w PVA fibers, the room-temperature storage modulus (E') increased by a factor of 4-5 in comparison to the neat PEBA, and they reveal a stepwise reduction of E' around the Tg of PVA (85 °C). This transition could indeed be utilized to fix a temporary shape and recover the permanent shape. At low strain, the fixity was 66 ± 14% and the recovery was 98 ± 2%. Overall, the data validate a simple and practical strategy for the fabrication of shape memory composites that involves a melt compaction process and employs two commercially available polymers.

  12. Improvement in Wood Bonding Strength of Poly (Vinyl Acetate-Butyl Acrylate Emulsion by Controlling the Amount of Redox Initiator

    Directory of Open Access Journals (Sweden)

    Yun Zhang

    2018-01-01

    Full Text Available Polyvinyl acetate emulsion adhesive has been widely used due to its good bonding performance and environmentally friendly properties. Indeed, the bonding performance can be further improved by copolymerizing with other monomers. In this study, the effect of the adjunction of redox initiator (hydrogen peroxide–tartaric acid, H2O2–TA on the properties of the poly (vinyl acetate-butyl acrylate (P (VAc–BA emulsion adhesive was investigated. With increasing dosage, the reaction became more complete and the obtained film was more compact, as identified via SEM. The core-shell structure of the emulsion particles was confirmed via TEM. Results indicate that while the initiator content increased from 0.5 to 1.0%, a clearer core-shell structure was obtained and the bonding strength of the plywood improved from 2.34 to 2.97 MPa. With the further incorporation of H2O2–TA (i.e., 1.5%, the bonding performance deteriorated. The optimum wood bonding strength (2.97 MPa of the prepared P (VAc-BA emulsion adhesive was even better than that (2.55 MPa of a commercial PVAc emulsion adhesive, suggesting its potential application for the wood industry.

  13. Prolonged Hypocalcemic Effect by Pulmonary Delivery of Calcitonin Loaded Poly(Methyl Vinyl Ether Maleic Acid Bioadhesive Nanoparticles

    Directory of Open Access Journals (Sweden)

    J. Varshosaz

    2014-01-01

    Full Text Available The purpose of the present study was to design a pulmonary controlled release system of salmon calcitonin (sCT. Therefore, poly(methyl vinyl ether maleic acid [P(MVEMA] nanoparticles were prepared by ionic cross-linking method using Fe2+ and Zn2+ ions. Physicochemical properties of nanoparticles were studied in vitro. The stability of sCT in the optimized nanoparticles was studied by electrophoretic gel method. Plasma calcium levels until 48 h were determined in rats as pulmonary-free sCT solution or nanoparticles (25 μg·kg−1, iv solution of sCT (5 μg·kg−1, and pulmonary blank nanoparticles. The drug remained stable during fabrication and tests on nanoparticles. The optimized nanoparticles showed proper physicochemical properties. Normalized reduction of plasma calcium levels was at least 2.76 times higher in pulmonary sCT nanoparticles compared to free solution. The duration of hypocalcemic effect of pulmonary sCT nanoparticles was 24 h, while it was just 1 h for the iv solution. There was not any significant difference between normalized blood calcium levels reduction in pulmonary drug solution and iv injection. Pharmacological activity of nanoparticles after pulmonary delivery was 65% of the iv route. Pulmonary delivery of P(MVEMA nanoparticles of sCT enhanced and prolonged the hypocalcemic effect of the drug significantly.

  14. Development of swellable local implants of a polyethyleneimine-poly(vinyl pyrrolidone) (PEI-PVP) hydrogel as a socket filler.

    Science.gov (United States)

    Chang, Ching-Wen; Ho, Hsiu-O; Lo, Yi-June; Lee, Sheng-Yang; Yang, You-Ren; Sheu, Ming-Thau

    2012-01-01

    In this study, hydrogels composed of polyethyleneimine (PEI) and poly(vinyl pyrrolidone) K90 (PVP) cross-linked with various concentrations (0, 0.125, 0.25 and 0.5%) of glutaraldehyde were evaluated as a hydrogel filler for the local delivery of lidocaine after tooth extraction. The drug-release kinetics, swellability, cytotoxicity and wound healing after tooth extraction of these non-cross-linked and cross-linked PEI-PVP hydrogels were examined in male beagles and compared to values using Spongostan(®). Results demonstrated that the extent of cross-linking influenced the swelling of the resulting hydrogel, but the drug-release rates were similar. No significant changes were observed in gingival fibroblasts in contact with the PEI- PVP hydrogels or Spongostan(®). In the in vivo study, PEI-PVP hydrogels showed good retention in the socket for 2 days and showed comparable wound-healing rates within 2 weeks with those of Spongostan(®). In conclusion, PEI-PVP hydrogels are suitable for use as socket-dressing materials, and the release of local anaesthesia from PEI-PVP hydrogels can be sustained for a desirable period of time to prevent pain after a tooth extraction.

  15. Therapeutic-Ultrasound-Triggered Shape Memory of a Melamine-Enhanced Poly(vinyl alcohol) Physical Hydrogel.

    Science.gov (United States)

    Li, Guo; Yan, Qiang; Xia, Hesheng; Zhao, Yue

    2015-06-10

    Therapeutic-ultrasound-triggered shape memory was demonstrated for the first time with a melamine-enhanced poly(vinyl alcohol) (PVA) physical hydrogel. The addition of a small amount of melamine (up to 1.5 wt %) in PVA results in a strong hydrogel due to the multiple H-bonding between the two constituents. A temporary shape of the hydrogel can be obtained by deformation of the hydrogel (∼65 wt % water) at room temperature, followed by fixation of the deformation by freezing/thawing the hydrogel under strain, which induces crystallization of PVA. We show that the ultrasound delivered by a commercially available device designed for the patient's pain relief could trigger the shape recovery process as a result of ultrasound-induced local heating in the hydrogel that melts the crystallized PVA cross-linking. This hydrogel is thus interesting for potential applications because it combines many desirable properties, being mechanically strong, biocompatible, and self-healable and displaying the shape memory capability triggered by a physiological stimulus.

  16. Bioinspired Hierarchical Alumina-Graphene Oxide-Poly(vinyl alcohol) Artificial Nacre with Optimized Strength and Toughness.

    Science.gov (United States)

    Wang, Jinrong; Qiao, Jinliang; Wang, Jianfeng; Zhu, Ying; Jiang, Lei

    2015-05-06

    Due to hierarchical organization of micro- and nanostructures, natural nacre exhibits extraordinary strength and toughness, and thus provides a superior model for the design and fabrication of high-performance artificial composite materials. Although great progress has been made in constructing layered composites by alternately stacking hard inorganic platelets and soft polymers, the real issue is that the excellent strength of these composites was obtained at the sacrifice of toughness. In this work, inspired by the layered aragonite microplatelets/chitin nanofibers-protein structure of natural nacre, alumina microplatelets-graphene oxide nanosheets-poly(vinyl alcohol) (Al2O3/GO-PVA) artificial nacre is successfully constructed through layer-by-layer bottom-up assembly, in which Al2O3 and GO-PVA act as "bricks" and "mortar", respectively. The artificial nacre has hierarchical "brick-and-mortar" structure and exhibits excellent strength (143 ± 13 MPa) and toughness (9.2 ± 2.7 MJ/m(3)), which are superior to those of natural nacre (80-135 MPa, 1.8 MJ/m(3)). It was demonstrated that the multiscale hierarchical structure of ultrathin GO nanosheets and submicrometer-thick Al2O3 platelets can deal with the conflict between strength and toughness, thus leading to the excellent mechanical properties that cannot be obtained using only one size of platelet. We strongly believe that the work presented here provides a creative strategy for designing and developing new composites with excellent strength and toughness.

  17. Effective immobilization of redox mediators in a poly (vinyl alcohol) matrix by using gamma-irradiation cross-linking

    International Nuclear Information System (INIS)

    Galiatsatos, C.; Mark, J.E.; Heineman, W.R.

    1987-01-01

    The development of electrodes with specific chemical properties by coating them with polymeric networks is the long-range goal of this research. Polymeric networks result from inserting chemical bonds between segments of different poly (vinyl alcohol) (PVAL) chains using gamma irradiation. The resulting three dimensional network adheres to the surface of graphite electrodes and therefore can be used as a convenient polymer matrix for the attachment and immobilization of electroactive redox molecules such as mediators. Two mediators, methyl viologen (MV) and 2,6-dichlorophenolindophenol (DCIP) were dissolved in aqueous solutions of PVAL and applied on electrode surfaces. The resulting electrodes were subjected to different irradiation doses. The irradiated PVAL/MV and PVAL/DCIP electrodes were evaluated for the following features: 1) effect of irradiation dose, 2) film thickness, 3) polymer/mediator ratio and 4) lifetime. For the radiation dose range 0-80 Mrad the PVAL/MV electrode exhibited a % BE varying between 14.3 (0 Mrads) and Mrads) and 52.0 (40 Mrads) while the PVAL/DCIP electrode varied between 5.3 (80 Mrads) and 31.3 (20 Mrads). This study suggests a way of immobilizing redox mediators in a PVAL matrix on surfaces of graphite electrodes

  18. Surfactant-Assisted Perovskite Nanofillers Incorporated in Quaternized Poly (Vinyl Alcohol Composite Membrane as an Effective Hydroxide-Conducting Electrolyte

    Directory of Open Access Journals (Sweden)

    Selvaraj Rajesh Kumar

    2017-05-01

    Full Text Available Perovskite LaFeO3 nanofillers (0.1% are incorporated into a quaternized poly(vinyl alcohol (QPVA matrix for use as hydroxide-conducting membranes in direct alkaline methanol fuel cells (DAMFCs. The as-synthesized LaFeO3 nanofillers are amorphous and functionalized with cetyltrimethylammonium bromide (CTAB surfactant. The annealed LaFeO3 nanofillers are crystalline without CTAB. The QPVA/CTAB-coated LaFeO3 composite membrane shows a defect-free structure while the QPVA/annealed LaFeO3 film has voids at the interfaces between the soft polymer and rigid nanofillers. The QPVA/CTAB-coated LaFeO3 composite has lower methanol permeability and higher ionic conductivity than the pure QPVA and QPVA/annealed LaFeO3 films. We suggest that the CTAB-coated LaFeO3 provides three functions to the polymeric composite: increasing polymer free volume, ammonium group contributor, and plasticizer to enhance the interfacial compatibility. The composite containing CTAB-coated LaFeO3 results in superior cell performance. A maximum power density of 272 mW cm−2 is achieved, which is among the highest power outputs reported for DAMFCs in the literature.

  19. Influence of inorganic salts mixture and a commercial additive on the degradation of poly(vinyl chloride)

    International Nuclear Information System (INIS)

    Silva, Williams B. da; Vasconcelos, Henrique M. de; Aquino, Katia Aparecida da S.; Araujo, Elmo S. de

    2009-01-01

    Samples of commercial poly(vinyl chloride) (PVC) containing a Hindered Amine Stabilizer (HAS) and samples containing a salt mixture of CuCl 2 /KI both in 0.1, 0.3, 0.5 and 0.7wt% concentration of HAS or salt mixture were investigated. The samples were irradiated with gamma radiation ( 60 Co) at room temperature in air at 25 kGy, sterilization dose of PVC medical supplies. The viscosity-average molecular weight (Mv) was analyzed by viscosity technique. Comparison of viscosity results obtained before and after irradiation ( at 25 kGy) of PVC showed crosslinking effect is predominant. On the other hand the PVC-HAS systems and PVC-salt systems showed a decrease in Mv values on irradiated samples reflecting the main chain random scissions effect. However the PVC-salt at 0.5wt% concentration showed no significant degradation index value. This result suggests that salt keeps the good radiolytic stabilization behavior of gamma-irradiated PVC and the HAS additive is not efficient on radiolytic stabilization of PVC. The CuCl 2 /KI mixture at 0.5wt% in the PVC matrix influenced the thermal behavior of the polymer increasing of 42 deg C in maximum thermal degradation temperature. In addition, the salt mixture influences significantly the Young's Modulus of PVC increasing the rigidity of polymer. (author)

  20. Interpenetrating network hydrogel membranes of sodium alginate and poly(vinyl alcohol) for controlled release of prazosin hydrochloride through skin.

    Science.gov (United States)

    Kulkarni, Raghavendra V; Sreedhar, V; Mutalik, Srinivas; Setty, C Mallikarjun; Sa, Biswanath

    2010-11-01

    Interpenetrating network (IPN) hydrogel membranes of sodium alginate (SA) and poly(vinyl alcohol) (PVA) were prepared by solvent casting method for transdermal delivery of an anti-hypertensive drug, prazosin hydrochloride. The prepared membranes were thin, flexible and smooth. The X-ray diffraction studies indicated the amorphous dispersion of drug in the membranes. Differential scanning calorimetric analysis confirmed the IPN formation and suggests that the membrane stiffness increases with increased concentration of glutaraldehyde (GA) in the membranes. All the membranes were permeable to water vapors depending upon the extent of cross-linking. The in vitro drug release study was performed through excised rat abdominal skin; drug release depends on the concentrations of GA in membranes. The IPN membranes extended drug release up to 24 h, while SA and PVA membranes discharged the drug quickly. The primary skin irritation and skin histopathology study indicated that the prepared IPN membranes were less irritant and safe for skin application. Copyright © 2010 Elsevier B.V. All rights reserved.

  1. Borax mediated layer-by-layer self-assembly of neutral poly(vinyl alcohol) and chitosan.

    Science.gov (United States)

    Manna, Uttam; Patil, Satish

    2009-07-09

    We report a multilayer film of poly(vinyl alcohol) (PVA)-borate complex and chitosan by using a layer-by-layer approach. PVA is an uncharged polymer, but hydroxyl functional groups of PVA can be cross-linked by using borax as a cross-linking agent. As a result electrostatic charges and intra- and interchain cross-links are introduced in the PVA chain and provide physically cross-linked networks. The PVA-borate was then deposited on a flat substrate as well as on colloidal particles with chitosan as an oppositely charged polyelectrolyte. Quartz crystal microbalance, scanning electron microscopy, and atomic force microscopy were used to follow the growth of thin film on flat substrate. Analogous experiments were performed on melamine formaldehyde colloidal particles (3-3.5 microm) to quantify the process for the preparation of hollow microcapsules. Removal of the core in 0.1 N HCl results in hollow microcapsules. Characterization of microcapsules by transmission electron microscopy revealed formation of stable microcapsules. Further, self-assembly of PVA-borate/chitosan was loaded with the anticancer drug doxorubicin, and release rates were determined at different pH values to highlight the drug delivery potential of this system.

  2. Consequences of poly(vinyl chloride) presence on the thermochemical process of lignocellulosic biomass in CO₂ by thermogravimetric analysis.

    Science.gov (United States)

    He, Yao; Ma, Xiaoqian; Zeng, Guangbo

    2015-02-01

    The thermochemical processes of lignocellulosic biomass and its mixtures with poly(vinyl chloride) (PVC) fractions were investigated by thermogravimetric analysis in CO2 atmosphere. Superposition property was assumed to examine whether and/or to what extent interactions occurred during the mixture decomposition. Results showed that interactions existed, of which the intensities changed with reaction stage, heating rate and PVC quantity, and they actively behaved toward the decomposition in most cases. With PVC presence, lignocellulosic biomass turned from three-stage to four-stage decomposition process where the reactions occurred at lower temperatures with heightened intensity, especially in the first stage. The measured activation energies calculated by Ozawa-Flynn-Wall and Vyazovkin methods were of minor difference <5 kJ/mol, and comparing them between materials in each stage confirmed the results of interaction impact. This work provides a theoretical basis bringing about the possibilities of recycling CO2 into a reaction medium of thermo-treatment of lignocellulosic material with PVC contaminants. Copyright © 2014 Elsevier Ltd. All rights reserved.

  3. Radiation synthesis of size-controlled poly(N-vinyl pyrrolidone) nanogels and their use as antimicrobial agents

    International Nuclear Information System (INIS)

    Isik, S.D.; Gueven, O.

    2011-01-01

    Complete text of publication follows. Nanogels are swollen networks of hydrophilic polymers generally developed to carry drugs, proteins and biologically active substances for biomedical applications. They can be prepared by 1) physical assembling of interactive polymers, 2) polymerization of monomers in micro or nanoscale environment, 3) crosslinking of preformed polymers, 4) template-assisted nanofabrication of nanogel particles. Among these methods crosslinking of preformed polymer chains provide excellent applications, especially when ionizing radiation is used as the tool to induce crosslinking. Due to its low cytotoxicity, excellent biocompatibility and non-carcinogenic and non-allergic properties, poly(N-vinyl pyrrolidone) (PVP) has been widely used in biomedical applications, hence the main reason for its selection in this work for the synthesis of its nanogels. PVP nanogels were prepared by gamma irradiation of its dilute aqueous solutions up to 15 kGy. The coil sizes of PVP chains were initially controlled by using acetone/water mixture as the solvent and further irradiations fixed the sizes by intramolecular crosslinking. By changing the concentration of PVP solutions, solvent composition and dose it was possible to prepare nanogels within 40-230 nm sizes. The nanogels were characterized by dynamic light scattering, scanning electron microscopy and atomic force microscopy. GPC has also been used to follow the changes in the coil sizes and distributions upon irradiations. The PVP nanogels thus synthesized were complexed with iodine in aqueous KI-I 2 solutions. Nanogels comprised of typical PVP-iodine complexes were tested for their antiseptic properties.

  4. Photostabilizing Efficiency of Poly(vinyl chloride in the Presence of Organotin(IV Complexes as Photostabilizers

    Directory of Open Access Journals (Sweden)

    Mustafa M. Ali

    2016-08-01

    Full Text Available Three organotin complexes containing furosemide as a ligand (L, Ph3SnL, Me2SnL2 and Bu2SnL2, were synthesized and characterized. Octahedral geometry was proposed for the Me2SnL2 and Bu2SnL2, while the Ph3SnL complex has trigonal bipyramid geometry. The synthesized organotin complexes (0.5% by weight were used as additives to improve the photostability of poly(vinyl chloride, PVC, (40 μm thickness upon irradiation. The changes imposed on functional groups, weight loss and viscosity average molecular weight of PVC films were monitored. The experimental results show that the rate of photodegradation was reduced in the presence of the organotin additives. The quantum yield of the chain scission was found to be low (9.8 × 10−7 when Ph3SnL was used as a PVC photostabilizer compared to controlled PVC (5.18 × 10−6. In addition, the atomic force microscope images for the PVC films containing Ph3SnL2 after irradiation shows a smooth surface compared to the controlled films. The rate of PVC photostabilization was found to be highest for Ph3SnL followed by Bu2SnL2 and Me2SnL2. It has been suggested that the organotin complexes could act as hydrogen chloride scavengers, ultraviolet absorbers, peroxide decomposers and/or radical scavengers.

  5. Synthesis and characterization of core-shell gold nanoparticles with poly(vinyl pyrrolidone) from a new precursor salt

    Science.gov (United States)

    Behera, M.; Ram, S.

    2013-02-01

    In this article, we report a facile one-step chemical synthesis of gold (Au) nanoparticles (GNPs) from a new precursor salt i.e., gold hydroxide in the presence of poly(vinyl pyrrolidone) (PVP) polymer. The non-aqueous dispersion of GNPs was comprehensively characterized by UV-Visible, FTIR, zeta potential, and transmission electron microscope (TEM). A strong surface plasmon resonance band at 529 nm in the UV-Visible spectrum confirms the formation of GNPs in the Au colloid. The FTIR spectroscopic results showed that PVP molecules get chemisorbed onto the surface of GNP via O-atom of carbonyl group. A negative zeta potential of (-)16 mV reveals accumulation of nonbonding electrons of O-atom of carbonyl group of PVP molecules on the nanosurface of GNP. TEM images demonstrate a core-shell nanostructure with an Au-crystalline core covered by a thin amorphous PVP-shell. PVP-capped GNPs could be a potential candidate for bio-sensing, catalysis, and other applications.

  6. Characterization and enhancement of the electrical performance of radiation modified poly (vinyl alcohol/gelatin copolymer films doped with carotene

    Directory of Open Access Journals (Sweden)

    S. Lotfy

    2014-07-01

    Full Text Available A series of poly (vinyl alcohol/gelatin copolymer (PVA/Gel with different entrapped carotene (Carot concentration into the films has been devised. The films were irradiated with γ-rays at dose levels of 10, 50, 100, 150 and 250 kGy. The crystalline and chemical structures of the samples have been studied using XRD and FTIR techniques. The direct current electrical conductivity (σDC has been determined from the proposed sampling before and after gamma exposure. It is clearly demonstrated that the electrical conductivity of PVA/Gel/Carot films was increased from two to three orders of magnitude due to carotene doping, and decreased one order of magnitude due to gamma radiation. The obtained results can be attributed to the existence of the conjugated double bonds in the aliphatic side chain of the carotene molecule. Thus, this work suggests the possibility of the use of the gamma irradiated PVA/Gel/Carot films in different electronic applications.

  7. Electromechanical behavior of polyaniline/poly (vinyl alcohol) blend films under static, dynamic and time-dependent strains

    International Nuclear Information System (INIS)

    Akhilesan, S; Lakshmana Rao, C; Varughese, S

    2014-01-01

    We report on the experimentally observed electrical conductivity enhancement in polyaniline/poly (vinyl alcohol) blend films under uniaxial tensile loading. Polyaniline (PANI) is an intrinsically conducting polymer, which does not form stretchable free-standing films easily and hence its electromechanical characterization is a challenge. Blending of PANI with other insulating polymers is a good choice to overcome the processability problem. We report the electromechanical response of solution blended and HCl doped PANI/PVA blends subjected to uniaxial, static, dynamic and time-dependent tensile loading. The demonstrated viscoelastic and morphological contributions of the component polymers to the electrical conductivity behavior in these blends could lead to interesting applications in strain sensors and flexible electronics. The reversibility of the electromechanical response under dynamic strain is found to increase in blends with higher PANI content. Time-dependent conductivity studies during mechanical stress relaxation reveal that variations in the micro-domain ordering and the relative relaxation rate of the individual polymer phases can give rise to interesting electrical conductivity changes in PANI blends. From morphological and electrical conductivity studies, we show that PANI undergoes primary and secondary agglomeration behavior in these blends that contributes to the changes in conductivity behavior during the deformation. A 3D variable range hopping (VRH) process, which uses a deformable core and shell concept based on blend morphology analysis, is used to explain the experimentally observed electromechanical behavior. (papers)

  8. Investigation of Zinc Oxide-Loaded Poly(Vinyl Alcohol) Nanocomposite Films in Tailoring Their Structural, Optical and Mechanical Properties

    Science.gov (United States)

    Aslam, Muhammad; Kalyar, Mazhar Ali; Raza, Zulfiqar Ali

    2018-04-01

    Wurtzite ZnO nanoparticles, as a nanofiller, were incorporated in a poly(vinyl alcohol) (PVA) matrix to prepare multipurpose nanocomposite films using a solution casting approach. Some advanced analytical techniques were used to investigate the properties of prepared nanocomposite films. The mediation of ZnO nanofillers resulted in modification of structural, optical and mechanical properties of nanocomposite films. A comprehensive band structure investigation might be useful for designing technological applications like in optoelectronic devices. The experimental results were found to be closely dependent on the nanofiller contents. Some theoretical models like Tauc's and Wemple-DiDomenico, were employed to investigate the band structure parameters. The imaginary part of the dielectric constant was used to investigate the band gap. Then, the Helpin-Tsai model was employed to predict Young's moduli of the prepared nanocomposite films. On 3 wt.% ZnO nanofiller loading, the optical band gap of the PVA-based nanocomposite film was decreased from 5.26 eV to 3 eV, the tensile strength increased from 25.3 MPa to 48 MPa and Young's modulus increased from 144 MPa to 544 MPa.

  9. Chromo- and fluorophoric water-soluble polymers and silica particles by nucleophilic substitution reaction of poly(vinyl amine

    Directory of Open Access Journals (Sweden)

    Katja Hofmann

    2010-07-01

    Full Text Available Novel chromophoric and fluorescent carbonitrile-functionalized poly(vinyl amine (PVAm and PVAm/silica particles were synthesized by means of nucleophilic aromatic substitution of 8-oxo-8H-acenaphtho[1,2-b]pyrrol-9-carbonitrile (1 with PVAm in water. The water solubility of 1 has been mediated by 2,6-O-β-dimethylcyclodextrin or by pre-adsorption onto silica particles. Furthermore, 1 was converted with isopropylamine into the model compound 1-M. All new compounds were characterized by NMR, FTIR, UV–vis and fluorescence spectroscopy. The solvent-dependent UV–vis absorption and fluorescence emission band positions of the model compound and the carbonitrile-functionalized PVAm were studied and interpreted using the empirical Kamlet–Taft solvent parameters π* (dipolarity/polarizability, α (hydrogen-bond donating capacity and β (hydrogen-accepting ability in terms of the linear solvation energy relationship (LSER. The solvent-independent regression coefficients a, b and s were determined using multiple linear correlation analysis. It is shown, that the chains of the polymer have a significant influence on the solvatochromic behavior of 1-P. The structure of the carbonitrile 1-Si bound to polymer-modified silica particles was studied by means of X-ray photoelectron spectroscopy (XPS and Brunauer–Emmett–Teller (BET measurements. Fluorescent silica particles were obtained as shown by fluorescence spectroscopy with a diffuse reflectance technique.

  10. Preparation and characterization of novel biocompatible cryogels of poly (vinyl alcohol) and egg-albumin and their water sorption study.

    Science.gov (United States)

    Bajpai, A K; Saini, Rajesh

    2006-01-01

    Polyvinyl alcohol (PVA) and egg albumin are water-soluble, biocompatible and biodegradable polymers and have been widely employed in biomedical fields. In this paper, novel physically cross-linked hydrogels composed of poly (vinyl alcohol) and egg albumin were prepared by cyclic freezing/thawing processes of aqueous solutions containing PVA and egg albumin. The FTIR analysis of prepared cryogels indicated that egg albumin was successfully introduced into the formed hydrogel possibly via hydrogen bonds among hydroxyl groups, amide groups and amino groups present in PVA and egg albumin. The gels were also characterized thermally and morphologically by DSC and SEM-techniques, respectively. The prepared so called 'cryogels' were evaluated for their water uptake potential and influence of various factors such as chemical architecture of the spongy hydrogels, pH and temperature of the swelling bath were investigated on the degree of water sorption by the cryogels. The effect of salt solution and various simulated biological fluids on the swelling of cryogel was also studied. The in vitro biocompatibility of the prepared cryogel was also judged by methods such as protein (BSA) adsorption, blood clot formation and percentage hemolysis measurements.

  11. The Effects of Orientation on the Mechanical and Morphological Properties of Woven Kenaf-reinforced Poly Vinyl Butyral Film

    Directory of Open Access Journals (Sweden)

    Suhad D. Salman

    2015-12-01

    Full Text Available Kenaf is one of the important plants cultivated for natural fibres globally and is regarded as an industrial crop in Malaysia for various applications. This study was conducted to determine the effects of orientation on the tensile and flexural strengths, Charpy impact test, and morphological properties of kenaf fibre-reinforced poly vinyl butyral (PVB composites. Laminates of 40% fibre weight fraction were manufactured using the hot press manufacturing technique at 0˚/90˚ and 45˚/−45˚ orientations, and eight specimens were prepared for each test. The mechanical properties of the composites were variably affected by the fibre orientation angle. The results showed that the composites at 0o/90o had the highest tensile strength, flexural strength, and flexural modulus, while the elongation at break was almost the same. Additionally, tests were carried out on the composites to determine their impact energy and impact strength. The results revealed that impact properties were affected in markedly different ways by different orientations. The composite at 45˚/−45˚ offered better impact properties than the composites at 0˚/90˚. In addition, scanning electron microscopy for impact specimens was employed to demonstrate the different failures in the fracture surfaces.

  12. Topological and morphological analysis of gamma rays irradiated chitosan-poly (vinyl alcohol) blends using atomic force microscopy

    International Nuclear Information System (INIS)

    Bhatt, Rinkesh; Bisen, D.S.; Bajpai, R.; Bajpai, A.K.

    2017-01-01

    In the present communication, binary blends of poly (vinyl alcohol) (PVA) and chitosan (CS) were prepared by solution cast method and the roughness parameters of PVA, native CS and CS-PVA blend films were determined using atomic force microscopy (AFM). Moreover, the changes in the morphology of the samples were also investigated after irradiation of gamma rays at absorbed dose of 1 Mrad and 10 Mrad for the scanning areas of 5×5 µm 2 , 10×10 µm 2 and 20×20 µm 2 . Amplitude, statistical and spatial parameters, including line, 3D and 2D image profiles of the experimental surfaces were examined and compared to un-irradiated samples. For gamma irradiated CS-PVA blends the larger waviness over the surface was found as compared to un-irradiated CS-PVA blends but the values of average roughness for both the films were found almost same. The coefficient of skewness was positive for gamma irradiated CS-PVA blends which revealed the presence of more peaks than valleys on the blend surfaces. - Highlights: • Binary polymer blends of chitosan and PVA were prepared. • Irradiation by gamma rays exhibited a significant change in surface morphology. • Various topographical and morphological parameters were investigated. • The prepared irradiated blends may find biomedical applications.

  13. Patterned cell arrays and patterned co-cultures on polydopamine-modified poly(vinyl alcohol) hydrogels

    International Nuclear Information System (INIS)

    Beckwith, Kai M; Sikorski, Pawel

    2013-01-01

    Live cell arrays are an emerging tool that expand traditional 2D in vitro cell culture, increasing experimental precision and throughput. A patterned cell system was developed by combining the cell-repellent properties of polyvinyl alcohol hydrogels with the cell adhesive properties of self-assembled films of dopamine (polydopamine). It was shown that polydopamine could be patterned onto spin-cast polyvinyl alcohol hydrogels by microcontact printing, which in turn effectively patterned the growth of several cell types (HeLa, human embryonic kidney, human umbilical vein endothelial cells (HUVEC) and prostate cancer). The cells could be patterned in geometries down to single-cell confinement, and it was demonstrated that cell patterns could be maintained for at least 3 weeks. Furthermore, polydopamine could be used to modify poly(vinyl alcohol) in situ using a cell-compatible deposition buffer (1 mg mL −1 dopamine in 25 mM tris with a physiological salt balance). The treatment switched the PVA hydrogel from cell repellent to cell adhesive. Finally, by combining microcontact printing and in situ deposition of polydopamine, patterned co-cultures of the same cell type (HeLa/HeLa) and dissimilar cell types (HeLa/HUVEC) were realized through simple chemistry and could be studied over time. The combination of polyvinyl alcohol and polydopamine was shown to be an attractive route to versatile, patterned cell culture experiments with minimal infrastructure requirements and low complexity. (paper)

  14. Poly(methyl vinyl ether-alt-maleic acid)-functionalized porous silicon nanoparticles for enhanced stability and cellular internalization.

    Science.gov (United States)

    Shahbazi, Mohammad-Ali; Almeida, Patrick V; Mäkilä, Ermei; Correia, Alexandra; Ferreira, Mónica P A; Kaasalainen, Martti; Salonen, Jarno; Hirvonen, Jouni; Santos, Hélder A

    2014-03-01

    Currently, developing a stable nanocarrier with high cellular internalization and low toxicity is a key bottleneck in nanomedicine. Here, we have developed a successful method to covalently conjugate poly(methyl vinyl ether-co-maleic acid) (PMVE-MA) copolymer on the surface of (3-aminopropyl)triethoxysilane-functionalized thermally carbonized porous silicon nanoparticles (APSTCPSi NPs), forming a surface negatively charged nanovehicle with unique properties. This polymer conjugated NPs could modify surface smoothness, charge, and hydrophilicity of the developed NPs, leading to considerable improvement in the colloidal and plasma stabilities via enhanced suspensibility and charge repulsion. Furthermore, despite the surface negative charge of the polymer-conjugated NPs, the cellular internalization was increased in both MDA-MB-231 and MCF-7 breast cancer cells. These results provide a proof-of-concept evidence that such polymer-based PSi nanocomposite can be extensively used as a promising candidate for intracellular drug delivery. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  15. Effect of irradiation on poly(vinyl chloride)/epoxidized natural rubber blend in the presence of additives: FTIR analysis

    International Nuclear Information System (INIS)

    Chantara Thevy Ratnam; Khairul Zaman Dahlan; Baharin, A.; Nasir, M.

    2001-01-01

    The effect of irradiation on the structure of 50/50 poly(vinyl chloride)/epoxidized natural rubber blend (PVC/ENR) was studied using the Fourier Transform Spectroscopy (FTIR). The 50/50 PVC/ENR blend was irradiated by using 3.0 MeV electron beam machine at 0 and 200 kGy irradiation doses. The influence of several additives such as TMPTA, Irganox 1010, and tribasic lead sulfate on the irradiation induced changes of the blend was investigated. It was found that upon irradiation, ring opening of the epoxide groups, oxidation as well crosslinking at residual double bonds occurred, leading to decreases in the intensities of the epoxide and cis double bond bands and an increases in ether and furan bands. The addition of Irganox 1010 and tribasic lead sulfate were found to inhibit the irradiation-induced reaction in the blend to a considerable extent. The importance of TMPTA in preventing the intramolecular ring opening side chain reaction was also discussed. However, studies did not reveal the exact nature of the irradiation-induced reactions involved in the blend. (Author)

  16. Topological and morphological analysis of gamma rays irradiated chitosan-poly (vinyl alcohol) blends using atomic force microscopy

    Science.gov (United States)

    Bhatt, Rinkesh; Bisen, D. S.; Bajpai, R.; Bajpai, A. K.

    2017-04-01

    In the present communication, binary blends of poly (vinyl alcohol) (PVA) and chitosan (CS) were prepared by solution cast method and the roughness parameters of PVA, native CS and CS-PVA blend films were determined using atomic force microscopy (AFM). Moreover, the changes in the morphology of the samples were also investigated after irradiation of gamma rays at absorbed dose of 1 Mrad and 10 Mrad for the scanning areas of 5×5 μm2, 10×10 μm2 and 20×20 μm2. Amplitude, statistical and spatial parameters, including line, 3D and 2D image profiles of the experimental surfaces were examined and compared to un-irradiated samples. For gamma irradiated CS-PVA blends the larger waviness over the surface was found as compared to un-irradiated CS-PVA blends but the values of average roughness for both the films were found almost same. The coefficient of skewness was positive for gamma irradiated CS-PVA blends which revealed the presence of more peaks than valleys on the blend surfaces.

  17. Physically crosslinked poly(vinyl alcohol-hydroxyethyl starch blend hydrogel membranes: Synthesis and characterization for biomedical applications

    Directory of Open Access Journals (Sweden)

    El-Refaie Kenawy

    2014-07-01

    Full Text Available Poly(vinyl alcohol, PVA is a polymer of great importance because of its many appealing characteristics specifically for various pharmaceutical and biomedical applications. Physically crosslinked hydrogel membranes composed of different amounts of hydroxyethyl starch (HES in (PVA and ampicillin were prepared by applying freeze–thawing method. This freezing–thawing cycle was repeated for three consecutive cycles. Physicochemical properties of PVA–HES membrane gel such as gel fraction, swelling, morphology, elongation, tensile strength, and protein adsorption were investigated. Introducing HES into freeze–thawed PVA structure affected crystal size distribution of PVA; and hence physicochemical properties and morphological structure have been affected. Increased HES concentration decreased the gel fraction %, maximum strength and break elongation. Indeed it resulted into a significant incrementing of the swelling ability, amount of protein adsorption, broader pore size, and pore distribution of membrane morphological structure. Furthermore, an increase in HES concentration resulted in better and still lower thermal stability compared to virgin PVA and freeze–thawed PVA. The maximum weight loss of PVA–HES hydrogel membranes ranged between 18% and 60% according to HES content, after two days of degradation in phosphate buffer saline (PBS, which indicates they are biodegradable. Thus, PVA–HES hydrogel membranes containing ampicillin could be a novel approach for biomedical application e.g. wound dressing purposes.

  18. Radiation grafting of hydrophilic monomers on to plasticized poly(vinyl chloride) sheets: Pt. 1

    International Nuclear Information System (INIS)

    Kalliyana Krishnan, V.; Jayakrishnan, A.; Francis, J.D.

    1990-01-01

    Medical-grade plasticized polyvinyl chloride (PVC) sheets were surface modified using gamma-radiation grafting of a combination of hydrophilic monomers based on 2-hydroxyethyl methacrylate (HEMA) and N-vinyl pyrrolidone (NVP). The properties of the modified surfaces were evaluated using contact angle measurements, phase-contrast photomicroscopy and scanning electron microscopy. Surface energy calculations indicated that the surfaces became highly hydrophilic when grafted with even a 1% (v/v) solution of HEMA-NVP combination in the presence of 0.005 M CuSO 4 . Migration of the plasticizer di(2-ethylhexyl phthalate) from the grafted sheets was examined in hydrocarbon solvents such as n-hexane, n-heptane and n-octane and in extractant media such as cotton seed oil and polyethylene glycol-400 (PEG-400). The migration was found to be 0 C over a period of 5 h. Accelerated leaching studies in cotton seed oil and PEG-400 demonstrated that virtually no plasticizer migrated out in the former over a period of 96 h whereas the rate of migration in the latter medium showed only a mild reduction. The migration behaviour was Fickian in nature for grafted sheets. The method described may be useful as a simple, versatile technique for preventing plasticizer migration from plasticized PVC for medical applications. (author)

  19. Influence of fiber content on mechanical, morphological and thermal properties of kenaf fibers reinforced poly(vinyl chloride)/thermoplastic polyurethane poly-blend composites

    International Nuclear Information System (INIS)

    El-Shekeil, Y.A.; Sapuan, S.M.; Jawaid, M.; Al-Shuja’a, O.M.

    2014-01-01

    Highlights: • Increasing fiber content decreased tensile strength and strain. • Tensile modulus was increasing with increase in fiber content. • SEM showed fiber/matrix poor adhesion. • Impact strength was decreasing with increase in fiber content. • Lower thermal stability with increase in fiber content was observed. - Abstract: Kenaf (Hibiscus Cannabinus) bast fiber reinforced poly(vinyl chloride) (PVC)/thermoplastic polyurethane (TPU) poly-blend was prepared by melt mixing method using Haake Polydrive R600 internal mixer. The composites were prepared with different fiber content: 20%, 30% and 40% (by weight), with the processing parameters: 140 °C, 11 min, and 40 rpm for temperature, time and speed, respectively. After mixing, the composite was compressed using compressing molding machine. Mechanical properties (i.e. tensile properties, flexural properties, impact strength) were studied. Morphological properties of tensile fracture surface were studied using Scanning electron microscope (SEM). Thermal properties of the composites were studied using Thermogravimetric Analyses (TGA). PVC/TPU/KF composites have shown lower tensile strength and strain with increase in fiber content. Tensile modulus showed an increasing trend with increase in fiber content. Impact strength decreased with increase in fiber content; however, high impact strength was observed even with 40% fiber content (20.2 kJ/m 2 ). Mean while; the 20% and 30% fiber contents showed higher impact strength of 34.9, 27.9 kJ/m 2 ; respectively. SEM showed that there is poor fiber/matrix adhesion. Thermal degradation took place in three steps. In the first step, composites as well as the matrix had a similar stability. At the second step, matrix showed a slightly better stability than the composites. At the last step, composites showed a better stability than the matrix

  20. Fabrication of novel high performance ductile poly(lactic acid) nanofiber scaffold coated with poly(vinyl alcohol) for tissue engineering applications.

    Science.gov (United States)

    Abdal-Hay, Abdalla; Hussein, Kamal Hany; Casettari, Luca; Khalil, Khalil Abdelrazek; Hamdy, Abdel Salam

    2016-03-01

    Poly(lactic acid) (PLA) nanofiber scaffold has received increasing interest as a promising material for potential application in the field of regenerative medicine. However, the low hydrophilicity and poor ductility restrict its practical application. Integration of hydrophilic elastic polymer onto the surface of the nanofiber scaffold may help to overcome the drawbacks of PLA material. Herein, we successfully optimized the parameters for in situ deposition of poly(vinyl alcohol), (PVA) onto post-electrospun PLA nanofibers using a simple hydrothermal approach. Our results showed that the average fiber diameter of coated nanofiber mat is about 1265±222 nm, which is remarkably higher than its pristine counterpart (650±180 nm). The hydrophilicity of PLA nanofiber scaffold coated with a PVA thin layer improved dramatically (36.11±1.5°) compared to that of pristine PLA (119.7±1.5°) scaffold. The mechanical testing showed that the PLA nanofiber scaffold could be converted from rigid to ductile with enhanced tensile strength, due to maximizing the hydrogen bond interaction during the heat treatment and in the presence of PVA. Cytocompatibility performance of the pristine and coated PLA fibers with PVA was observed through an in vitro experiment based on cell attachment and the MTT assay by EA.hy926 human endothelial cells. The cytocompatibility results showed that human cells induced more favorable attachment and proliferation behavior on hydrophilic PLA composite scaffold than that of pristine PLA. Hence, PVA coating resulted in an increase in initial human cell attachment and proliferation. We believe that the novel PVA-coated PLA nanofiber scaffold developed in this study, could be a promising high performance biomaterial in regeneration medicine. Copyright © 2015. Published by Elsevier B.V.

  1. Compliant gel polymer electrolyte based on poly(methyl acrylate-co-acrylonitrile)/poly(vinyl alcohol) for flexible lithium-ion batteries

    International Nuclear Information System (INIS)

    Ma, Xianguo; Huang, Xinglan; Gao, Jiandong; Zhang, Shu; Deng, Zhenghua; Suo, Jishuan

    2014-01-01

    Highlights: •Compliant gel polymer electrolyte based on P(MA-co-AN)/PVA is facilely prepared for flexible lithium-ion batteries. •The compliant gel polymer electrolyte displays high ionic conductivity, self-standing and mechanical flexible. •The compliant gel polymer electrolyte exhibits excellent chemical and electrochemical performances. -- Abstract: In this report, mechanically compliant gel polymer electrolyte (GPE) for flexible lithium-ion batteries is facilely fabricated. The GPE that based on the poly(methyl acrylate-co-acrylonitrile)/poly(vinyl alcohol) (P(MA-co-AN)/PVA) was prepared via emulsion polymerization. Herein, the P(MA-co-AN) copolymer is anticipated to exert beneficial for the bendability of the GPE, as well as swollen with the liquid electrolyte to provide a facile pathway for ion movement. The PVA serves as a stabilizer during the emulsion polymerization and a mechanical framework for the compliant polymer membrane. Performance benefits of the mechanically compliant membrane are elucidated in terms of mechanical behavior, thermostability and ionic conductivity. The GPE is still self-standing and mechanical flexible after swollen with liquid electrolyte. The GPE displays a conductivity of 0.98 mS cm −1 with the uptake electrolyte up to 150% of its own weight at 30 °C, excellent electrochemical stability window (5.2 V vs. Li/Li + ) and favorable interfacial characteristics. When used in flexible lithium-ion batteries, such a GPE demonstrates satisfactory compatibility with LiCoO 2 and graphite electrodes

  2. Absorbed energy for radiation crosslinking in stabilized PE systems

    International Nuclear Information System (INIS)

    Novakovic, Lj.; Gal, O.; Charlesby, A.

    1990-01-01

    A quantitative consideration on the absorbed energy consumption in various γ-irradiated polyethylene systems is given. On the base of the increased gel dose values for the PE systems containing antioxidant, relative to the gel doses for the pure polymers, the surplus of the absorbed energy due to the presence of the particular antioxidant is calculated. The increasing of the energy consumption in the stabilized systems depends on both the type and the content of the basic polymer. The surplus in the absorbed energy decreases with the radiation dose increasing, reflecting both the diminishing of the antioxidant concentration in the irradiating PE systems and the crosslinking level. The findings can be of interest in the estimation of the absorbed doses for the specific radiation crosslinking processes. (author)

  3. Absorbed energy for radiation crosslinking in stabilized PE systems

    Energy Technology Data Exchange (ETDEWEB)

    Novakovic, Lj; Gal, O [Institut za Nuklearne Nauke Boris Kidric, Belgrade (Yugoslavia); Charlesby, A

    1990-01-01

    A quantitative consideration on the absorbed energy consumption in various {gamma}-irradiated polyethylene systems is given. On the base of the increased gel dose values for the PE systems containing antioxidant, relative to the gel doses for the pure polymers, the surplus of the absorbed energy due to the presence of the particular antioxidant is calculated. The increasing of the energy consumption in the stabilized systems depends on both the type and the content of the basic polymer. The surplus in the absorbed energy decreases with the radiation dose increasing, reflecting both the diminishing of the antioxidant concentration in the irradiating PE systems and the crosslinking level. The findings can be of interest in the estimation of the absorbed doses for the specific radiation crosslinking processes. (author).

  4. Shape memory behaviour of radiation-crosslinked PCL/PMVS blends

    International Nuclear Information System (INIS)

    Zhu Guangming; Xu Shuogui; Wang Jinhua; Zhang Longbin

    2006-01-01

    The performance and radiation crosslinking of polycaprolactone (PCL) and polymethylvinylsiloxane (PMVS) blends has been investigated. Radiation crosslinking of PCL/PMVS blends followed the Charlesby-Pinner equation, and PMVS promoted the radiation crosslinking of the blends. As the concentration of PMVS increased, the gelation dose and the ratio of degradation to crosslinking (p 0 /q 0 ) decreased and the efficiency of radiation crosslinking increased. The elastic modulus below the melting point of PCL of radiation-crosslinked PCL/PMVS blends decreased with the increase of PMVS, and increased above the melting point. The crosslinked PCL/PMVS blends exhibited excellent shape memory effects, and the ratios of deformation to recovery were more than 95%

  5. The effect of chain flexibility and chain mobility on radiation crosslinking reactions of polymers

    International Nuclear Information System (INIS)

    Sun Jiazhen

    2003-01-01

    Flexibility of polymer chains is an important factor to effects of radiation crosslinking of the polymer. Polymers with flexible chains are easier to be crosslinked, with lower dose of gelation, than polymers with more rigid chains. And it is known that most polymers with abnormal rigidity can be radiation-crosslinked only at high temperatures when the molecular chains get enough mobility. The flexibility of polymer chains also influences the relationship between degree of degradation and radiation dose. A chain flexibility factor β has been introduced to modify the Charlesby-Pinner equation of sol-fraction and radiation dose. The new relationship equation applies to a wider range of polymers in radiation crosslinking. Studies also show that for flexible polymers with lower T g and molecular internal rotating factor, mechanism of radiation crosslinking is mainly in H type, whereas for rigid polymers with higher T g and molecular internal rotating factor, mechanism of radiation crosslinking is mainly in T type

  6. PENGARUH TEMPERATUR TERHADAP TINGKAT SERAPAN AIR DALAM BAHAN POLY (2-VINYL PYRIDINE -CO-STYRENE

    Directory of Open Access Journals (Sweden)

    Mr Wiendartun

    2015-01-01

    Full Text Available Hydrophilic properties of organic polymer such as Poly (2-Vinylpyridine- Co-Styrene have been found to have a correlation with other physical properties especially the electric resistivity. In this work, we have studied one of the physical properties of a polymer material, Poly (2-Vinylpyridine- Co-Styrene, that is the electric resistivity. It was studied on the basis of its relation with the concentration, temperature, humidity and the distance between their electrodes. The sample fabricated consists of two types of consentration: 0.03 gr/ml and 0.05 gr/ml with the distance between the two electrodes are 0.40 mm and 0.80 mm respectively. Towards these samples, we investigated the resistance coefficient for every 2% change in humidity for both drying and watering processes. From the experiment we obtain the following results: 1 There is hysteresis during the watering and drying processes indicating the continuity of resistance of this material, 2 Sample with smaller distance of electrodes performs better than that of the longer ones, 3 Sample fabricated from solution with higher concentration performs better than that of the lower ones, 4 Room temperature plays a significant role on the performance of the polymer material between the associated electrodes. These results could be used as a stepping-stone toward the more advance research leading the determination of film stability, resistancy upon temperature variation etc, so that this polymer material could be further developed into the humidity sensor device material. Key words: Hydrophilic, electric resistance, humidity sensor and polymer.

  7. Bioinspired design and macroscopic assembly of poly(vinyl alcohol)-coated graphene into kilometers-long fibers

    Science.gov (United States)

    Kou, Liang; Gao, Chao

    2013-05-01

    Nacre is characterized by its excellent mechanical performance due to the well-recognized ``brick and mortar'' structure. Many efforts have been applied to make nacre-mimicking materials, but it is still a big challenge to realize their continuous production. Here, we prepared sandwich-like building blocks of poly(vinyl alcohol) (PVA)-coated graphene, and achieved high-nanofiller-content kilometers-long fibers by continuous wet-spinning assembly technology. The fibers have a strict ``brick and mortar'' layered structure, with graphene sheet as rigid brick and PVA as soft mortar. The mortar thickness can be precisely tuned from 2.01 to 3.31 nm by the weight feed ratio of PVA to graphene, as demonstrated by both atomic force microscopy and X-ray diffraction measurements. The mechanical strength of the nacre-mimicking fibers increases with increasing the content of PVA, and it rises gradually from 81 MPa for the fiber with 53.1 wt% PVA to 161 MPa for the fiber with 65.8 wt% PVA. The mechanical performance of our fibers was independent of the molecular weight (MW) of PVA in the wide range of 2-100 kDa, indicating that low MW polymers can also be used to make strong nanocomposites. The tensile stress of fibers immersed in PVA 5 wt% solution reached ca. 200 MPa, surpassing the values of nacre and most of other nacre-mimicking materials. The nacre-mimicking fibers are highly electrically conductive (~350 S m-1) after immersing in hydroiodic acid, enabling them to connect a circuit to illuminate an LED lamp.Nacre is characterized by its excellent mechanical performance due to the well-recognized ``brick and mortar'' structure. Many efforts have been applied to make nacre-mimicking materials, but it is still a big challenge to realize their continuous production. Here, we prepared sandwich-like building blocks of poly(vinyl alcohol) (PVA)-coated graphene, and achieved high-nanofiller-content kilometers-long fibers by continuous wet-spinning assembly technology. The fibers

  8. Preparation and characterization of chitosan/genipin/poly(N-vinyl-2-pyrrolidone) films for controlled release drugs

    Energy Technology Data Exchange (ETDEWEB)

    Aldana, Ana Agustina, E-mail: aaldana@fcq.unc.edu.ar [Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Nacional de Cordoba (UNC), Edificio de Ciencias II, Medina Allende y Haya de la Torre, Ciudad Universitaria, Cordoba 5000 (Argentina); Gonzalez, Agustin, E-mail: agustingonzalez@fcq.unc.edu.ar [Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Nacional de Cordoba (UNC), Edificio de Ciencias II, Medina Allende y Haya de la Torre, Ciudad Universitaria, Cordoba 5000 (Argentina); Strumia, Miriam C., E-mail: mcs@fcq.unc.edu.ar [Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Nacional de Cordoba (UNC), Edificio de Ciencias II, Medina Allende y Haya de la Torre, Ciudad Universitaria, Cordoba 5000 (Argentina); Martinelli, Marisa, E-mail: mmartinelli@fcq.unc.edu.ar [Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Nacional de Cordoba (UNC), Edificio de Ciencias II, Medina Allende y Haya de la Torre, Ciudad Universitaria, Cordoba 5000 (Argentina)

    2012-05-15

    Highlights: Black-Right-Pointing-Pointer Cross-linked chitosan films using genipin and/or PVP. Black-Right-Pointing-Pointer Propranolol hydrochloride was used like a model drug to release studies. Black-Right-Pointing-Pointer Incorporating PVP improves mechanical and diffusion properties. Black-Right-Pointing-Pointer Ch-Gen 0.10% and Ch-Gen 0.10%-PVP have optimal behavior. - Abstract: The study of the physicochemical and functional properties of chitosan films cross-linked with genipin and poly(N-vinyl-2-pyrrolidone) (PVP) was performed in this work. Cross-linked films were prepared by casting method from acetic acid solutions. The structure and physical properties of the films were analyzed by infrared spectroscopy (FT-IR), nuclear magnetic resonance spectroscopy ({sup 13}C NMR), differential scanning calorimetry (DSC) and mechanical testings. Propranolol hydrochloride was used like a model drug to determine the behavior of drug release from films. The drug release capacity was measured and compared with the degree of cross-linking, mechanical properties and swelling index. There was an appropriate balance of hydrophilicity, mechanical properties and diffusion by the incorporation of PVP into the networks cross-linked with genipin. The combination of both cross-linkers allows obtaining a soft and tough material potentially applicable as a controlled release. This research represents the first report where both cross-linkers, chemical and ionic agents, are used for obtaining films. These studies suggest that the chitosan films prepared here are promising drug delivery systems for buccal application, with thermal stability and acceptable mechanical properties. Buccal films may be preferred in terms of flexibility and comfort.

  9. Comparative Evaluation of the Antimicrobial Efficacy of Three Immersion Chemical Disinfectants on Clinically Derived Poly(Vinyl Siloxane) Impressions.

    Science.gov (United States)

    Jeyapalan, Vidhya; Krishnan, Chitra Shankar; Ramasubramanian, Hariharan; Sampathkumar, Jayakrishnakumar; Azhagarasan, N S; Krishnan, Madhusudan

    2016-07-06

    To comparatively evaluate the antimicrobial efficacy of freshly prepared electrolyzed oxidizing water (EOW) with that of 2.4% glutaraldehyde (GA) and 1% sodium hypochlorite (SH) on clinically derived poly vinyl siloxane (PVS) impressions. Four clinically derived PVS impressions each were obtained from 10 subjects. One impression from each subject was randomly kept as control (group I), without disinfection. The remaining three impressions were randomly disinfected by immersion in either 2.4% GA (group II), 1% SH (group III), or freshly prepared EOW (group IV). The samples were subjected to microbial culture individually on brain heart infusion (BHI) agar medium. The organisms isolated were confirmed by visual examination and gram staining. Mean colony forming units (CFU) were counted, log 10 reduction obtained and compared. Data were statistically analyzed using one-way ANOVA, followed by multiple comparisons using Tukey-HSD post hoc tests (p < 0.05). Streptococci, Staphylococci, Pseudomonas, Candida, Proteus, Klebsiella, and E. coli were isolated from all impressions including the controls, except those disinfected by EOW. All three disinfectants showed significant reduction in CFU and log 10 reduction values as compared to the controls. EOW showed significantly higher reduction in log 10 values compared to GA and SH, whereas GA and SH showed similar reductions. EOW, GA, and SH showed kill rates of 100%, 99.60%, and 99.82%, respectively. EOW showed significant antimicrobial efficacy as evidenced by reduction in log 10 values when used as an immersion disinfectant for PVS impressions when compared with the results obtained using GA and SH. These results need further investigation. EOW shows high antimicrobial efficacy when used as an immersion disinfectant as compared to GA and SH for clinically derived PVS impressions. © 2016 by the American College of Prosthodontists.

  10. Preparation and characterization of chitosan/genipin/poly(N-vinyl-2-pyrrolidone) films for controlled release drugs

    International Nuclear Information System (INIS)

    Aldana, Ana Agustina; González, Agustín; Strumia, Miriam C.; Martinelli, Marisa

    2012-01-01

    Highlights: ► Cross-linked chitosan films using genipin and/or PVP. ► Propranolol hydrochloride was used like a model drug to release studies. ► Incorporating PVP improves mechanical and diffusion properties. ► Ch–Gen 0.10% and Ch–Gen 0.10%–PVP have optimal behavior. - Abstract: The study of the physicochemical and functional properties of chitosan films cross-linked with genipin and poly(N-vinyl-2-pyrrolidone) (PVP) was performed in this work. Cross-linked films were prepared by casting method from acetic acid solutions. The structure and physical properties of the films were analyzed by infrared spectroscopy (FT-IR), nuclear magnetic resonance spectroscopy ( 13 C NMR), differential scanning calorimetry (DSC) and mechanical testings. Propranolol hydrochloride was used like a model drug to determine the behavior of drug release from films. The drug release capacity was measured and compared with the degree of cross-linking, mechanical properties and swelling index. There was an appropriate balance of hydrophilicity, mechanical properties and diffusion by the incorporation of PVP into the networks cross-linked with genipin. The combination of both cross-linkers allows obtaining a soft and tough material potentially applicable as a controlled release. This research represents the first report where both cross-linkers, chemical and ionic agents, are used for obtaining films. These studies suggest that the chitosan films prepared here are promising drug delivery systems for buccal application, with thermal stability and acceptable mechanical properties. Buccal films may be preferred in terms of flexibility and comfort.

  11. Properties of iopamidol-incorporated poly(vinyl alcohol) microparticle as an X-ray imaging flow tracer.

    Science.gov (United States)

    Ahn, Sungsook; Jung, Sung Yong; Lee, Jin Pyung; Lee, Sang Joon

    2011-02-10

    We have recently reported on poly(vinyl alcohol) microparticles containing X-ray contrast agent, iopamidol, designed as a flow tracer working in synchrotron X-ray imaging ( Biosens. Bioelectron. 2010 , 25 , 1571 ). Although iopamidol is physically encapsulated in the microparticles, it displays a great contrast enhancement and stable feasibility in in vitro human blood pool. Nonetheless, a direct relation between the absolute amount of incorporated iopamidol and the enhancement in imaging efficiency was not observed. In this study, physical properties of the designed microparticle are systematically investigated experimentally with theoretical interpretation to correlate an enhancement in X-ray imaging efficiency. The compositional ratio of X-ray contrast agent in polymeric microparticle is controlled as 1/1 and 10/1 [contrast agent/polymer microparticle (w/w)] with changed degree of cross-linkings. Flory-Huggins interaction parameter (χ), retractive force (τ) and degree of swelling of the designed polymeric microparticles are investigated. In addition, the hydrodynamic size (D(H)) and ζ-potential are evaluated in terms of environment responsiveness. The physical properties of the designed flow tracer microparticles under a given condition are observed to be strongly related with the X-ray absorption efficiency, which are also supported by the Beer-Lambert-Bouguer law. The designed microparticles are almost nontoxic with a reasonable concentration and time period, enough to be utilized as a flow tracer in various biomedical applications. This study would contribute to the basic understanding on the physical property connected with the imaging efficiency of contrast agents.

  12. A novel reutilization method for waste printed circuit boards as flame retardant and smoke suppressant for poly (vinyl chloride)

    Energy Technology Data Exchange (ETDEWEB)

    Xiu, Fu-Rong, E-mail: xiu_chem@hotmail.com [College of Ecological Environment and Urban Construction, Fujian University of Technology, Fuzhou 350108 (China); Weng, Huiwei; Qi, Yingying; Yu, Gending; Zhang, Zhigang [College of Ecological Environment and Urban Construction, Fujian University of Technology, Fuzhou 350108 (China); Zhang, Fu-Shen [Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China)

    2016-09-05

    Highlights: • We report a novel electronic waste-based flame retardant for PVC. • The SCWO-treated PCBs significantly improves the flame retardancy of PVC. • The flame retardant mechanism of SCWO-treated PCBs was studied. • Appropriate amount flame retardant does not degrade the mechanical property of PVC. - Abstract: In this study, a novel reutilization method for waste printed circuit boards (PCBs) as flame retardant and smoke suppressant for poly (vinyl chloride) (PVC) was successfully testified. A supercritical water oxidation (SCWO) process was applied to treat waste PCBs before they could be used as flame retardants of PVC. The results indicated that SCWO conditions had a significant effect on the flame retarding and smoke suppressing properties of waste PCBs for PVC. Cu{sub 2}O, CuO, and SnO{sub 2} were the main active ingredients in waste PCBs-derived flame retardants. A conversion of Cu elements (Cu{sup 0} → Cu{sup +} → Cu{sup 2+}) during SCWO process with the increase of reaction temperature was found to be the key influence factor for the flame retarding properties of SCWO-treated PCBs. The experiment results also showed that there was a synergistic effect of flame retardancy between Cu{sup +} and Cu{sup 2+}. After the optimized SCWO treatment, SCWO-treated PCBs significantly improved the flame retardancy and smoke suppression of PVC. Limiting oxygen index (LOI) and char yield (CY) increased with increasing SCWO-treated PCBs content in PVC, while smoke density rating (SDR) and maximum smoke density (MSD) decreased markedly. The mechanical properties of PVC samples were influenced in different degree by adding different content SCWO-treated PCBs.

  13. Structural, mechanical and electrical properties biopolymer blend nanocomposites derived from poly (vinyl alcohol)/cashew gum/magnetite

    Science.gov (United States)

    Ramesan, M. T.; Jayakrishnan, P.; Manojkumar, T. K.; Mathew, G.

    2018-01-01

    Blending of poly vinyl alcohol (PVA) and natural biopolymers such as cashew gum (CG) with magnetite (Fe3O4) nanoparticles has been a promising way for preparing bio-degradable polymeric blend nanocomposites. PVA/CG/Fe3O4 blend nanocomposites have been prepared by a simple solution casting technique using water as the green solvent. The characterization of blend nanocomposites has been carried out by using Fourier transform infrared, UV, x-ray diffraction (XRD), high resolution transmission electron microscopy, scanning electron microscopy (SEM), differential scanning calorimetry, thermogravimetric analysis, mechanical properties and electrical conductivity. The interaction between nanoparticles and the blend segments was confirmed from the shift in characteristic absorption peaks of nanocomposites compared to PVA/CG blend. XRD analysis has shown the presence of crystalline peaks of nanoparticles in the blend matrix. The uniform distribution of Fe3O4 nanoparticles in the blend was revealed by TEM and SEM. The strong interaction of nanoparticles with the blend has been confirmed by the increase in glass transition temperature resulting from the reduced flexibility of the blend nanocomposite compared to that of the blend system. An increase in thermal stability and tensile strength and reduction in elongation at break of nanocomposites have been noticed with the increasing loading of nanoparticles. The AC electrical conductivity, dielectric constant and dielectric loss of the nanocomposites have been found to be higher than that of the blend. Generally, it can be stated that the magnetite nanoparticles acts as a potential filler in the PVA/CG blend at 7 wt% loading, giving the best balance of properties.

  14. Stability assessment of lyophilized intravenous immunoglobulin after reconstitution in glass containers and poly(vinyl chloride) bags.

    Science.gov (United States)

    Parti, R; Mankarious, S

    1997-02-01

    Human intravenous immunoglobulin (IGIV) has been in use for the past 20 years. This biological product is commonly provided in liquid or lyophilized dosage form. When the lyophilized product is rehydrated, it is usually administered within 2-3 h from time of complete dissolution. While this practice is advisable whenever possible, occasionally the patient or care-giver may need to delay the infusion. Hence, a study of the stability of lyophilized IGIV after reconstitution with water for injection was conducted. The reconstituted product was stored either in its original glass container or pooled into poly(vinyl chloride) (PVC) bags. The effect of extended storage on the active ingredient (IgG), excipients (glucose, albumin) and extractables [sodium from glass vials, and di-(2-ethyl-hexyl) phthalate and cyclohexanone from PVC bags] was evaluated. The stability of the active ingredient was evaluated by physico-chemical tests (molecularsize distribution, pH, appearance, total protein), monitoring titres of a specific antibody (hepatitis B surface antigen) and an antibody functional test (bacterial opsonization). To evaluate the risk of microbial contamination during reconstitution and pooling procedures, sterility, pyrogen and animal-safety tests were included in the protocol. The potential of IgG polymerizing in solution during storage and subsequent complement activation was evaluated by assaying for non-specific binding of complement (anti-complement activity). Results show that aseptically reconstituted IGIV is stable and remains sterile up to 48 h at 5 degrees C. The reconstituted product was also found to be stable at room temperature (25 degrees C) up to 12 h.

  15. Macroporous modified poly (vinyl alcohol) hydrogels with charged groups for tissue engineering: Preparation and in vitro evaluation

    Energy Technology Data Exchange (ETDEWEB)

    Drozdova, Maria G., E-mail: drozdovamg@gmail.com [Polymers for Biology Laboratory, Shemyakin & Ovchinnikov Institute of Bioorganic Chemistry of Russian Academy of Sciences, Miklukho-Maklaya str., 16/10, Moscow 117997 (Russian Federation); Zaytseva-Zotova, Daria S. [Polymers for Biology Laboratory, Shemyakin & Ovchinnikov Institute of Bioorganic Chemistry of Russian Academy of Sciences, Miklukho-Maklaya str., 16/10, Moscow 117997 (Russian Federation); Akasov, Roman A. [Polymers for Biology Laboratory, Shemyakin & Ovchinnikov Institute of Bioorganic Chemistry of Russian Academy of Sciences, Miklukho-Maklaya str., 16/10, Moscow 117997 (Russian Federation); Sechenov First Moscow State Medical University, Institute for Regenerative Medicine, Trubetskaya str., 8/2, Moscow 119048 (Russian Federation); Golunova, Anna S.; Artyukhov, Alexander A. [D. Mendeleyev University of Chemical Technology of Russia, Miusskaya Square 9, Moscow 125047 (Russian Federation); Udartseva, Olga O.; Andreeva, Elena R. [Institute of Biomedical Problems of Russian Academy of Sciences, Khoroshevskoe Shosse 76a, Moscow 123007 (Russian Federation); Lisovyy, Denis E.; Shtilman, Michael I. [D. Mendeleyev University of Chemical Technology of Russia, Miusskaya Square 9, Moscow 125047 (Russian Federation); Markvicheva, Elena A. [Polymers for Biology Laboratory, Shemyakin & Ovchinnikov Institute of Bioorganic Chemistry of Russian Academy of Sciences, Miklukho-Maklaya str., 16/10, Moscow 117997 (Russian Federation)

    2017-06-01

    Poly(vinyl alcohol) (PVA) hydrogels are widely employed for various biomedical applications, including tissue engineering, due to their biocompatibility, high water solubility, low protein adsorption, and chemical stability. However, non-charged surface of PVA-based hydrogels is not optimal for cell adhesion and spreading. Here, cross-linked macroporous hydrogels based on low molecular weight acrylated PVA (Acr-PVA) was synthesized by modification of the pendant alcohol groups on the PVA with glycidyl methacrylate (GMA). To enhance cell affinity, charged groups were introduced to the hydrogel composition. For this purpose, Acr-PVA was copolymerized with either negatively charged acrylic acid (AA) or positively charged 2-(diethylamino) ethyl methacrylate (DEAEMA) monomers. A surface charge of the obtained hydrogels was found to be in function of the co-monomer type and content. Confocal microscopy observations confirmed that adhesion and spreading of both mouse fibroblasts (L929) and human mesenchymal stem cells (hMSC) on the modified Acr-PVA-AA and Acr-PVA-DEAEMA hydrogels were better than those on the non-modified Acr-PVA hydrogel. The increase of DEAEMA monomer content from 5 to 15 mol% resulted in the enhancement of cell viability which was 1.5-fold higher for Acr-PVA-DEAEMA-15 hydrogel than that of the non-modified Acr-PVA hydrogel sample. - Highlights: • To enhance cell affinity, acrylated PVA hydrogel was modified with AA or DEAEMA monomers. • Cell adhesion and spreading were found to depend on the co-monomer type and content. • Proliferation of L929 fibroblasts and stem cells increased on the modified hydrogels.

  16. Optical and structural properties of radiolytically in situ synthesized silver nanoparticles stabilized by chitosan/poly(vinyl alcohol) blends

    International Nuclear Information System (INIS)

    Krstić, Jelena; Spasojević, Jelena; Radosavljević, Aleksandra; Šiljegovć, Milorad; Kačarević-Popović, Zorica

    2014-01-01

    In this study, the potential of chitosan/poly(vinyl alcohol) (CS/PVA) blends as capping agent for stabilization of Ag-nanoparticles (Ag NPs) during their in situ gamma irradiation induced synthesis was investigated. The UV–vis absorption spectra show the surface plasmon absorption band around 410 nm, which confirms the formation of Ag-nanoparticles. It was found that the composition of CS/PVA blend affected the size of the obtained Ag-nanoparticles, as well as the parameters such as density, molar concentration and effective surface area, calculated from the experimentally obtained UV–vis absorption spectra and spectra obtained by simulation according to the Mie theory. SEM micrograph and XRD measurement indicated a spherical morphology and face centered cubic crystal structure of Ag-nanoparticles, with diameter around 12 nm. The values of optical band gap energy between valence and conduction bands (E g ), calculated from the UV–vis absorption spectra, also show dependence on the blend composition for Ag–CS/PVA colloids as well as for Ag–CS/PVA nanocomposites. - Highlights: • Ag NPs were synthesized by γ-irradiation and stabilized by CS/PVA blends. • Composition of CS/PVA blends has influence on the size of spherical Ag NPs. • simulation based on Mie theory was used to calculate the parameters of Ag NPs. • Ag NPs are stabilized through interactions with -OH and -NH 2 groups of polymers. • Optical band gap energy was calculated from UV–vis spectra by Tauc's expression

  17. Blends of nitrile butadiene rubber/poly (vinyl chloride: The use of maleated anhydride castor oil based plasticizer

    Directory of Open Access Journals (Sweden)

    Indiah Ratna Dewi

    2016-06-01

    Full Text Available Recently, much attention has been focused on research to replace petroleum-based plasticizers, with biodegradable materials, such as biopolymer which offers competitive mechanical properties. In this study, castor oil was modified with maleic anhydride (MAH to produce bioplasticizer named maleated anhydride castor oil (MACO, and used in nitrile butadiene rubber (NBR/poly vinyl chloride (PVC blend. The effect of MACO on its cure characteristics and mechanical properties of NBR/PVC blend has been determined. The reactions were carried out at different castor oil (CO/xylene ratios, i.e. 1:0 and 1:1 by weight, and fixed CO/MAH ratio, 1:3 by mole. DOP, CO, and MACO were added into each NBR/PVC blend according to the formula. It was found that the viscosity and safe process level of NBR/PVC blend is similar from all plasticizer, however, MACO (1:0 showed the highest cure rate index (CRI. MACO-based plasticizer gave a higher value of the mechanical properties of the NBR/PVC blend as compared to DOP based plasticizer. MACO (1:1 based plasticizer showed a rather significance performance compared to another type of plasticizers both before and after aging. The value of hardness, elongation at break, tensile strength, and tear strength were 96 Shore A, 155.91 %, 19.15 MPa, and 74.47 MPa, respectively. From this result, NBR/PVC blends based on MACO plasticizer can potentially replace the DOP, and therefore, making the rubber blends eco-friendly.

  18. FTIR studies of plasticized poly(vinyl alcohol)-chitosan blend doped with NH 4NO 3 polymer electrolyte membrane

    Science.gov (United States)

    Kadir, M. F. Z.; Aspanut, Z.; Majid, S. R.; Arof, A. K.

    2011-03-01

    Fourier transform infrared (FTIR) spectroscopy studies of poly(vinyl alcohol) (PVA), and chitosan polymer blend doped with ammonium nitrate (NH 4NO 3) salt and plasticized with ethylene carbonate (EC) have been performed with emphasis on the shift of the carboxamide, amine and hydroxyl bands. 1% acetic acid solution was used as the solvent. It is observed from the chitosan film spectrum that evidence of polymer-solvent interaction can be observed from the shifting of the carboxamide band at 1660 cm -1 and the amine band at 1591 cm -1 to 1650 and 1557 cm -1 respectively and the shift of the hydroxyl band from 3377 to 3354 cm -1. The hydroxyl band in the spectrum of PVA powder is observed at 3354 cm -1 and is observed at 3343 cm -1 in the spectrum of the PVA film. On addition of NH 4NO 3 up to 30 wt.%, the carboxamide, amine and hydroxyl bands shifted from 1650, 1557 and 3354 cm -1 to 1642, 1541 and 3348 cm -1 indicating that the chitosan has complexed with the salt. In the PVA-NH 4NO 3 spectrum, the hydroxyl band has shifted from 3343 to 3272 cm -1 on addition of salt from 10 to 30 wt.%. EC acts as a plasticizing agent since there is no shift in the bands as observed in the spectrum of PVA-chitosan-EC films. The mechanism of ion migration is proposed for the plasticized and unplasticized PVA-chitosan-NH 4NO 3 systems. In the spectrum of PVA-chitosan-NH 4NO 3-EC complex, the doublet C dbnd O stretching in EC is observed in the vicinity 1800 and 1700. This indicates that there is some interaction between the salt and EC.

  19. A novel reutilization method for waste printed circuit boards as flame retardant and smoke suppressant for poly (vinyl chloride)

    International Nuclear Information System (INIS)

    Xiu, Fu-Rong; Weng, Huiwei; Qi, Yingying; Yu, Gending; Zhang, Zhigang; Zhang, Fu-Shen

    2016-01-01

    Highlights: • We report a novel electronic waste-based flame retardant for PVC. • The SCWO-treated PCBs significantly improves the flame retardancy of PVC. • The flame retardant mechanism of SCWO-treated PCBs was studied. • Appropriate amount flame retardant does not degrade the mechanical property of PVC. - Abstract: In this study, a novel reutilization method for waste printed circuit boards (PCBs) as flame retardant and smoke suppressant for poly (vinyl chloride) (PVC) was successfully testified. A supercritical water oxidation (SCWO) process was applied to treat waste PCBs before they could be used as flame retardants of PVC. The results indicated that SCWO conditions had a significant effect on the flame retarding and smoke suppressing properties of waste PCBs for PVC. Cu_2O, CuO, and SnO_2 were the main active ingredients in waste PCBs-derived flame retardants. A conversion of Cu elements (Cu"0 → Cu"+ → Cu"2"+) during SCWO process with the increase of reaction temperature was found to be the key influence factor for the flame retarding properties of SCWO-treated PCBs. The experiment results also showed that there was a synergistic effect of flame retardancy between Cu"+ and Cu"2"+. After the optimized SCWO treatment, SCWO-treated PCBs significantly improved the flame retardancy and smoke suppression of PVC. Limiting oxygen index (LOI) and char yield (CY) increased with increasing SCWO-treated PCBs content in PVC, while smoke density rating (SDR) and maximum smoke density (MSD) decreased markedly. The mechanical properties of PVC samples were influenced in different degree by adding different content SCWO-treated PCBs.

  20. Macroporous modified poly (vinyl alcohol) hydrogels with charged groups for tissue engineering: Preparation and in vitro evaluation

    International Nuclear Information System (INIS)

    Drozdova, Maria G.; Zaytseva-Zotova, Daria S.; Akasov, Roman A.; Golunova, Anna S.; Artyukhov, Alexander A.; Udartseva, Olga O.; Andreeva, Elena R.; Lisovyy, Denis E.; Shtilman, Michael I.; Markvicheva, Elena A.

    2017-01-01

    Poly(vinyl alcohol) (PVA) hydrogels are widely employed for various biomedical applications, including tissue engineering, due to their biocompatibility, high water solubility, low protein adsorption, and chemical stability. However, non-charged surface of PVA-based hydrogels is not optimal for cell adhesion and spreading. Here, cross-linked macroporous hydrogels based on low molecular weight acrylated PVA (Acr-PVA) was synthesized by modification of the pendant alcohol groups on the PVA with glycidyl methacrylate (GMA). To enhance cell affinity, charged groups were introduced to the hydrogel composition. For this purpose, Acr-PVA was copolymerized with either negatively charged acrylic acid (AA) or positively charged 2-(diethylamino) ethyl methacrylate (DEAEMA) monomers. A surface charge of the obtained hydrogels was found to be in function of the co-monomer type and content. Confocal microscopy observations confirmed that adhesion and spreading of both mouse fibroblasts (L929) and human mesenchymal stem cells (hMSC) on the modified Acr-PVA-AA and Acr-PVA-DEAEMA hydrogels were better than those on the non-modified Acr-PVA hydrogel. The increase of DEAEMA monomer content from 5 to 15 mol% resulted in the enhancement of cell viability which was 1.5-fold higher for Acr-PVA-DEAEMA-15 hydrogel than that of the non-modified Acr-PVA hydrogel sample. - Highlights: • To enhance cell affinity, acrylated PVA hydrogel was modified with AA or DEAEMA monomers. • Cell adhesion and spreading were found to depend on the co-monomer type and content. • Proliferation of L929 fibroblasts and stem cells increased on the modified hydrogels.

  1. Bioinspired design and macroscopic assembly of poly(vinyl alcohol)-coated graphene into kilometers-long fibers.

    Science.gov (United States)

    Kou, Liang; Gao, Chao

    2013-05-21

    Nacre is characterized by its excellent mechanical performance due to the well-recognized "brick and mortar" structure. Many efforts have been applied to make nacre-mimicking materials, but it is still a big challenge to realize their continuous production. Here, we prepared sandwich-like building blocks of poly(vinyl alcohol) (PVA)-coated graphene, and achieved high-nanofiller-content kilometers-long fibers by continuous wet-spinning assembly technology. The fibers have a strict "brick and mortar" layered structure, with graphene sheet as rigid brick and PVA as soft mortar. The mortar thickness can be precisely tuned from 2.01 to 3.31 nm by the weight feed ratio of PVA to graphene, as demonstrated by both atomic force microscopy and X-ray diffraction measurements. The mechanical strength of the nacre-mimicking fibers increases with increasing the content of PVA, and it rises gradually from 81 MPa for the fiber with 53.1 wt% PVA to 161 MPa for the fiber with 65.8 wt% PVA. The mechanical performance of our fibers was independent of the molecular weight (MW) of PVA in the wide range of 2-100 kDa, indicating that low MW polymers can also be used to make strong nanocomposites. The tensile stress of fibers immersed in PVA 5 wt% solution reached ca. 200 MPa, surpassing the values of nacre and most of other nacre-mimicking materials. The nacre-mimicking fibers are highly electrically conductive (∼350 S m(-1)) after immersing in hydroiodic acid, enabling them to connect a circuit to illuminate an LED lamp.

  2. Proton exchange membrane developed from novel blends of polybenzimidazole and poly(vinyl-1,2,4-triazole).

    Science.gov (United States)

    Hazarika, Mousumi; Jana, Tushar

    2012-10-24

    In continuation (J. Phys. Chem. B2008, 112, 5305; J. Colloid Interface Sci. 2010, 351, 374) of our quest for proton exchange membrane (PEM) developed from polybenzimidazole (PBI) blends, novel polymer blend membranes of PBI and poly(1-vinyl-1,2,4-triazole) (PVT) were prepared using a solution blending method. The aim of the work was to investigate the effect of the blend composition on the properties, e.g., thermo-mechanical stability, swelling, and proton conductivity of the blend membranes. The presence of specific interactions between the two polymers in the blends were observed by studying the samples using varieties of spectroscopic techniques. Blends prepared in all possible compositions were studied using a differential scanning calorimetry (DSC) and exhibited a single T(g) value, which lies between the T(g) value of the neat polymers. The presence of a single composition-dependent T(g) value indicated that the blend is a miscible blend. The N-H···N interactions between the two polymers were found to be the driving force for the miscibility. Thermal stability up to 300 °C of the blend membranes, obtained from thermogravimetric analysis, ensured their suitability as PEMs for high-temperature fuel cells. The proton conductivity of the blend membranes have improved significantly, compared to neat PBI, because of the presence of triazole moiety, which acts as a proton facilitator in the conduction process. The blend membranes showed a considerably lower increase in thickness and swelling ratio than that of PBI after doping with phosphoric acid (PA). We found that the porous morphology of the blend membranes caused the loading of a larger amount of PA and, consequently, higher proton conduction with lower activation energy, compared to neat PBI.

  3. Evaluation of poly (vinyl alcohol) based cryogel–zinc oxide nanocomposites for possible applications as wound dressing materials

    Energy Technology Data Exchange (ETDEWEB)

    Chaturvedi, Archana [Bose Memorial Research Laboratory, Department of Chemistry, Government Autonomous Science College Jabalpur (India); Bajpai, Anil K., E-mail: akbmrl@yahoo.co.in [Bose Memorial Research Laboratory, Department of Chemistry, Government Autonomous Science College Jabalpur (India); Bajpai, Jaya [Bose Memorial Research Laboratory, Department of Chemistry, Government Autonomous Science College Jabalpur (India); Singh, Sunil K. [Department of Chemistry, Guru Ghasidas University, Bilaspur, CG (India)

    2016-08-01

    In this investigation cryogels composed of poly (vinyl alcohol) (PVA) were prepared by repeated freeze thaw method followed by in situ precipitation of zinc oxide nanoparticles within the cryogel networks. Fourier transformed infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD), Energy dispersive X-ray spectroscopy (EDX) were used to characterize the nanocomposites. The morphologies of native PVA cryogels and PVA cryogel-ZnO nanocomposites were observed by scanning electron microscopy (SEM), 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 zinc oxide nanoparticles with diameter < 100 nm. XRD results showed all relevant Bragg's reflections for crystal structure of zinc oxide nanoparticles. Thermo gravimetric-differential thermal analysis (TG-DTA) was conducted to evaluate thermal stability of the nanocomposites. Mechanical properties of nanocomposites were determined in terms of tensile strength and percent elongation. Biocompatible nature was ascertained by anti-haemolytic activity, bovine serum albumin (blood protein) adsorption and in vitro cytotoxicity tests. The prepared nanocomposites were also investigated for swelling and deswelling behaviours. The results revealed that both the swelling and deswelling process depend on the chemical composition of the nanocomposites, number of freeze-thaw cycles, pH and temperature of the swelling medium. The developed biocompatible PVA cryogel-ZnO nanocomposites were also tested for antibacterial activities against both Gram-negative and Gram-positive bacteria. - Highlights: • PVA–zinc oxide nanocomposites have been prepared with no chemical crosslinking. • The nanocomposites are completely biocompatible. • They also show antibacterial property. • The nanocomposites

  4. Lead removal from cathode ray tube glass by the action of calcium hydroxide and poly(vinyl chloride)

    International Nuclear Information System (INIS)

    Grause, Guido; Takahashi, Kenshi; Kameda, Tomohito; Yoshioka, Toshiaki

    2014-01-01

    Highlights: • About 99.9% of lead is removed from CRT glass by PbCl 2 volatilization. • PVC is used as chlorination agent with the aid of Ca(OH) 2 as HCl absorbing material. • The residual calcium silicate has a lead content as low as 140 mg kg −1 . • Lead leaching from the residue was below the detection limit. - Abstract: With the development of flat screen technology, the cathode ray tubes (CRTs) used in TV sets became obsolete, leaving huge amounts of lead-containing CRT glass for disposal. We developed a novel lead volatilization process in which PbCl 2 was generated in the presence of poly(vinyl chloride) (PVC) as a chlorination agent and Ca(OH) 2 as an HCl absorber. PVC was incinerated in air atmosphere and the resulting HCl was captured by Ca(OH) 2 before exiting the reactor with the air flow. CaCl 2 and Ca(OH) 2 reacted with the lead glass forming volatile PbCl 2 and crystalline Ca-silicates. Since the reactivity of lead glass with gaseous HCl is negligible, the presence of Ca(OH) 2 was essential for the success of this method. At a temperature of 1000 °C, a molar Cl/Pb ratio of 16, and a molar Ca/Si ratio of about 2, approximately 99.9% of the lead was volatilized, leaving a residue with a lead content of 140 mg kg −1 . The residual calcium silicate, with its low lead level, has the potential to be repurposed for other uses

  5. Studies on Radiation Synthesis of Poly(vinyl alcohol)- Natural Polysaccharides Hydrogel Wound Dressing

    International Nuclear Information System (INIS)

    Varshney, L.

    2006-01-01

    Radiation processed PVA-polysaccharides hydrogels have been observed to be suitable for producing transparent, flexible and mechanically strong, biocompatible, effective and economical hydrogel dressings(HD). The dressings were formed in single stage irradiation process achieving gel formation and sterilization at 25-30 kGy gamma radiation dose. No synthetic plasticizers and additives were used. Different formulations containing Poly-vinylalcohol, (PVA) and polysaccharides selected from combinations of agar and carrageenan were used to make the dressings. The selected polysaccharides themselves form thermo-reversible gels and degrade on irradiation. Using concentration of polysaccharides as low as 0.5 -2 % resulted in increase of tensile strength from 45 g/cm 2 to 400 g/cm 2 , elongation from 30 % to 410 % and water uptake from 25 % to 120% with respect to PVA gel without polysaccharides. Besides improving mechanical strength, agar contributes more to elongation and carrageenan to mechanical strength of the gel dressing. The polysaccharides show different pre-gel viscosities behaviour indicating different individual contribution to the PVA network. Increasing the concentration of agar in the formulation to about 2% converts the sheet gel to paste gel useful for filling wound cavities. The polysaccharides also provide desirable plasticizer and humectant effect into the dressing. Formulations containing 7-9% PVA, 0.5- 1.5 % carrageenan and 0.5-1% agar gave highly effective usable hydrogel dressings. Scanning Electron Micrographs show highly porous structure of the gel. Clinical trials of wound dressing on human patients established safety and efficacy of the dressing. The dressing has been observed to be useful in treating burns, non healing ulcers of Diabetes, Leprosy and other external wounds. The dressings are now being marketed in India under different brand names

  6. Fabrication of novel high performance ductile poly(lactic acid) nanofiber scaffold coated with poly(vinyl alcohol) for tissue engineering applications

    Energy Technology Data Exchange (ETDEWEB)

    Abdal-hay, Abdalla, E-mail: abda_55@jbnu.ac.kr [Dept of Engineering Materials and Mechanical Design, Faculty of Engineering, South Valley of University, Qena 83523 (Egypt); Hussein, Kamal Hany [Stem Cell Institute and College of Veterinary Medicine, Kangwon National University, Chuncheon, Gangwon 200-701 (Korea, Republic of); Casettari, Luca [Department of Biomolecular Sciences, University of Urbino, Piazza Rinascimento, 6, Urbino, PU 61029 (Italy); Khalil, Khalil Abdelrazek [Dept. of Mechanical Engineering, College of Engineering, King Saud University, 800, Riyadh 11421 (Saudi Arabia); Dept. of Mechanical Engineering, Faculty of Energy Engineering, Aswan University, Aswan (Egypt); Hamdy, Abdel Salam [Dept. of Manufacturing and Industrial Engineering, College of Engineering and Computer Science, University of Texas Rio Grande Valley, 1201 West University Dr., Edinburg, TX 78541-2999 (United States)

    2016-03-01

    Poly(lactic acid) (PLA) nanofiber scaffold has received increasing interest as a promising material for potential application in the field of regenerative medicine. However, the low (hydrophilicity) and poor ductility restrict its practical application. Integration of hydrophilic elastic polymer onto the surface of the nanofiber scaffold may help to overcome the drawbacks of PLA material. Herein, we successfully optimized the parameters for in situ deposition of poly(vinyl alcohol), (PVA) onto post-electrospun PLA nanofibers using a simple hydrothermal approach. Our results showed that the average fiber diameter of coated nanofiber mat is about 1265 ± 222 nm, which is remarkably higher than its pristine counterpart (650 ± 180 nm). The hydrophilicity of PLA nanofiber scaffold coated with a PVA thin layer improved dramatically (36.11 ± 1.5°) compared to that of pristine PLA (119.7 ± 1.5°) scaffold. The mechanical testing showed that the PLA nanofiber scaffold could be converted from rigid to ductile with enhanced tensile strength, due to maximizing the hydrogen bond interaction during the heat treatment and in the presence of PVA. Cytocompatibility performance of the pristine and coated PLA fibers with PVA was observed through an in vitro experiment based on cell attachment and the MTT assay by EA.hy926 human endothelial cells. The cytocompatibility results showed that human cells induced more favorable attachment and proliferation behavior on hydrophilic PLA composite scaffold than that of pristine PLA. Hence, PVA coating resulted in an increase in initial human cell attachment and proliferation. We believe that the novel PVA-coated PLA nanofiber scaffold developed in this study, could be a promising high performance biomaterial in regeneration medicine. - Highlights: • Novel PVA-coated PLA nanofibers were prepared by a simple hydrothermal route. • This in situ treatment strategy for PLA fibers induced polymer chain conformation. • Bonding interaction

  7. Fabrication of novel high performance ductile poly(lactic acid) nanofiber scaffold coated with poly(vinyl alcohol) for tissue engineering applications

    International Nuclear Information System (INIS)

    Abdal-hay, Abdalla; Hussein, Kamal Hany; Casettari, Luca; Khalil, Khalil Abdelrazek; Hamdy, Abdel Salam

    2016-01-01

    Poly(lactic acid) (PLA) nanofiber scaffold has received increasing interest as a promising material for potential application in the field of regenerative medicine. However, the low (hydrophilicity) and poor ductility restrict its practical application. Integration of hydrophilic elastic polymer onto the surface of the nanofiber scaffold may help to overcome the drawbacks of PLA material. Herein, we successfully optimized the parameters for in situ deposition of poly(vinyl alcohol), (PVA) onto post-electrospun PLA nanofibers using a simple hydrothermal approach. Our results showed that the average fiber diameter of coated nanofiber mat is about 1265 ± 222 nm, which is remarkably higher than its pristine counterpart (650 ± 180 nm). The hydrophilicity of PLA nanofiber scaffold coated with a PVA thin layer improved dramatically (36.11 ± 1.5°) compared to that of pristine PLA (119.7 ± 1.5°) scaffold. The mechanical testing showed that the PLA nanofiber scaffold could be converted from rigid to ductile with enhanced tensile strength, due to maximizing the hydrogen bond interaction during the heat treatment and in the presence of PVA. Cytocompatibility performance of the pristine and coated PLA fibers with PVA was observed through an in vitro experiment based on cell attachment and the MTT assay by EA.hy926 human endothelial cells. The cytocompatibility results showed that human cells induced more favorable attachment and proliferation behavior on hydrophilic PLA composite scaffold than that of pristine PLA. Hence, PVA coating resulted in an increase in initial human cell attachment and proliferation. We believe that the novel PVA-coated PLA nanofiber scaffold developed in this study, could be a promising high performance biomaterial in regeneration medicine. - Highlights: • Novel PVA-coated PLA nanofibers were prepared by a simple hydrothermal route. • This in situ treatment strategy for PLA fibers induced polymer chain conformation. • Bonding interaction

  8. Synthesis and Properties of the Metallo-Supramolecular Polymer Hydrogel Poly[methyl vinyl ether-alt-mono-sodium maleate]∙AgNO3

    KAUST Repository

    Al-Dossary, Mona S.

    2014-05-01

    Gels are a special class of materials which are composed of 3D networks of crosslinked polymer chains that encapsulate liquid/air in the matrix. They can be classified into organogels or hydrogels (organic solvent for organogel and water for hydrogel). For hydrogels that contain metallic elements in the form of ions, the term of metallo-supramolecular polymer hydrogel (MSPHG) is often used. The aim of this project is to develop a kind of new MSPHG and investigate its properties and possible applications. The commercial polymeric anhydride poly(methyl vinyl ether-alt-maleic anhydride) (PVM/MA) is converted by reaction with NaOH to give poly(methyl vinyl ether-alt-monosodium maleate) (PVM/Na-MA). By addition of AgNO3-solution, the formation of the silver(I) supramolecular polymer hydrogel poly[methyl vinyl ether-alt-mono-sodium maleate]∙AgNO3 is obtained. Freeze-dried samples of the hydrogel show a mesoporous network of polycarboxylate ligands that are crosslinked by silver(I) cations. The supercritical CO2 dried silver(I) hydrogel was characterized by FT-IR, SEM-EDAX, TEM, TGA and Physical adsorption (BET) measurements. The intact silver(I) hydrogel was characterized by cryo-SEM. In the intact hydrogel, ion-exchange studies are reported and it is shown that Ag+ ions can be exchanged by copper(II) cations without disintegration of the hydrogel. The silver(I) hydrogel shows effective antibacterial activity and potential application as burn wound dressing.

  9. The Impact of the Polymer Chain Length on the Catalytic Activity of Poly(N-vinyl-2-pyrrolidone)-supported Gold Nanoclusters

    OpenAIRE

    Haesuwannakij, Setsiri; Kimura, Tetsunari; Furutani, Yuji; Okumura, Kazu; Kokubo, Ken; Sakata, Takao; Yasuda, Hidehiro; Yakiyama, Yumi; Sakurai, Hidehiro

    2017-01-01

    Poly(N-vinyl-2-pyrrolidone) (PVP) of varying molecular weight (M w ?=?40-360?kDa) were employed to stabilize gold nanoclusters of varying size. The resulting Au:PVP clusters were subsequently used as catalysts for a kinetic study on the sized-dependent aerobic oxidation of 1-indanol, which was monitored by time-resolved in situ infrared spectroscopy. The obtained results suggest that the catalytic behaviour is intimately correlated to the size of the clusters, which in turn depends on the mol...

  10. Synthesis and properties of the metallo-supramolecular polymer hydrogel poly[methyl vinyl ether-alt-mono-sodium maleate]·AgNO3: Ag+/Cu2+ ion exchange and effective antibacterial activity

    KAUST Repository

    Xu, Feng

    2014-01-01

    The commercial polymeric anhydride poly(methyl vinyl ether-alt-maleic anhydride) (PVM/MA) is converted by reaction with NaOH to give poly(methyl vinyl ether-alt-mono-sodium maleate) (PVM/Na-MA). By addition of AgNO 3-solution, the formation of the silver(i) supramolecular polymer hydrogel poly[methyl vinyl ether-alt-mono-sodium maleate]·AgNO 3 is reported. Freeze-dried samples of the hydrogel show a mesoporous network of polycarboxylate ligands that are crosslinked by silver(i) cations. In the intact hydrogel, ion-exchange studies are reported and it is shown that Ag+ ions can be exchanged by copper(ii) cations without disintegration of the hydrogel. The silver(i) hydrogel shows effective antibacterial activity and potential application as burn wound dressing. © the Partner Organisations 2014.

  11. Preliminary study on radiation crosslinking of PE-NBR multiple phase system

    International Nuclear Information System (INIS)

    Wang Hong; Zhang Wanxi; Sun Jiazhen

    1989-01-01

    The effect of radiation crosslinking on the structure and properties of PE-NBR (polyethylene-acrylonitrile-butadiene rubber) multiple phase system was studied in this paper. The relationship of sol fraction and irradiated dose to multiplephase system was demonstrated

  12. Structural and optical characteristics of silver/poly(N-vinyl-2-pyrrolidone) nanosystems synthesized by γ-irradiation

    International Nuclear Information System (INIS)

    Jovanović, Željka; Radosavljević, Aleksandra; Šiljegović, Milorad; Bibić, Nataša; Mišković-Stanković, Vesna; Kačarević-Popović, Zorica

    2012-01-01

    Silver nanoparticles (AgNPs) were synthesized in situ by γ-irradiation using poly(N-vinyl-2-pyrrolidone) (PVP) as a capping agent. The concentration, molecular weight and the structure (crosslinked and interpenetrated network) of PVP were varied, in order to determine the influence of the capping agent in the radiolytic synthesis of the Ag/PVP nanosystems. Transmission electron microscopy (TEM) showed that AgNPs obtained from the solutions containing higher PVP concentration and higher molecular weight were spherical in shape, with narrow size distribution and a diameter of∼6 nm, while slightly larger rod-shaped silver agglomerates, with bimodal nanoparticle size distribution and diameters of ∼10 nm and ∼20 nm were obtained from the solutions containing lower PVP concentration and lower molecular weight. Strong plasmon coupling and extending of plasmon resonance was observed by UV–vis spectroscopy, as a result of formation of nanorod-like agglomerates. Crosslinked and interpenetrated network did not affect the structure of synthesized AgNPs. Ag/PVP nanocomposite, in the form of thin film, was obtained by solvent evaporation from Ag/PVP colloid solution with 10 wt% of PVP, and characterized by FTIR spectroscopy. The interactions in Ag/PVP nanocomposite are shown to be the result of the coordination bonding between AgNPs and nitrogen from pyrrolidone ring of PVP. The optical properties of investigated Ag/PVP nanosystems, as measured by the values of optical band gap, E g , are mainly the consequence of the interparticle distance as a result of the concentration and the structure of surrounding PVP macromolecules. - Highlights: ► AgNPs of different structure and optical properties were obtained by γ-irradiation. ► Different PVP concentration and molecular weight induced different structure. ► Rod-shaped AgNPs were obtained with lower PVP concentration and molecular weight. ► Stabilization by coordination bonding between AgNPs and N from pyrrolidone

  13. Migration of plasticizers from poly(vinyl chloride) and multilayer infusion bags using selective extraction and GC-MS.

    Science.gov (United States)

    Haned, Zohra; Moulay, Saad; Lacorte, Silvia

    2018-04-12

    Flexible poly(vinyl chloride) (PVC) is widely used in the pharmaceutical industry for the manufacture of medical devices (tubes, probes, bags, primary packaging, etc.). The objective of the present study was to develop a procedure to evaluate the migration potential of nine plastic additives in aqueous infusion bags (NaCl 0.9% and glucose 5%): five phthalates, one adipate, two alkylphenols, and benzophenone. Two types of materials were analyzed: (i) new and outdated plasticized PVC (containing 40% of diethylhexyl phthalate DEHP); and (ii) tri-laminate polyethylene-polyamide-polypropylene, a multilayer material presumably exempt from DEHP. In addition, we evaluated the migration of plasticizers from PVC raw materials (film and grain) under controlled conditions to compare the migration levels according to Regulation 2011/10. Solid phase extraction and liquid-liquid extraction with gas-chromatography coupled to mass spectrometry were used in all tests. The migration of DEHP in PVC grain exceeded the maximum regulated level of 5000 μg/kg, whereas the levels were much lower in films. In new PVC bags, DEHP was the only compound detected at 4.31 ± 0.5 μg/L in NaCl 0.9% and 4.29 ± 0.25 μg/L in glucose 5% serums, whereas the levels increased 10 times in three-year shelf-life bags. In multilayer bags, DEHP was not found but instead, two plasticizers were detected namely dibuthylphthalate (DBP) and diethylphthalate (DEP) at 0.7 ± 0.1 μg/L and 4.14 ± 0.6 μg/L, respectively. These plasticizers are not mentioned as additives allowed in materials intended for parenteral use (European Pharmacopoeia 8.0, 3.1.5. and 3.1.6.). Caprolactam was tentatively identified and could have stemmed from the polyamide of the multilayer composite. The levels of phthalates remained low but not negligible and might constitute a risk to public health in the case of reiterative infusions. Copyright © 2018. Published by Elsevier B.V.

  14. Fabrication of 3D interconnected porous TiO{sub 2} nanotubes templated by poly(vinyl chloride-g-4-vinyl pyridine) for dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Koh, Joo Hwan; Koh, Jong Kwan; Seo, Jin Ah; Kim, Jong Hak [Department of Chemical and Biomolecular Engineering, Yonsei University, 262 Seongsanno, Seodaemun-gu, Seoul 120-749 (Korea, Republic of); Shin, Jong-Shik, E-mail: jonghak@yonsei.ac.kr [Department of Biotechnology, Yonsei University, 262 Seongsanno, Seodaemun-gu, Seoul 120-749 (Korea, Republic of)

    2011-09-07

    Porous TiO{sub 2} nanotube arrays with three-dimensional (3D) interconnectivity were prepared using a sol-gel process assisted by poly(vinyl chloride-graft-4-vinyl pyridine), PVC-g-P4VP graft copolymer and a ZnO nanorod template. A 7 {mu}m long ZnO nanorod array was grown from the fluorine-doped tin oxide (FTO) glass via a liquid phase deposition method. The TiO{sub 2} sol-gel solution templated by the PVC-g-P4VP graft copolymer produced a random 3D interconnection between the adjacent ZnO nanorods during spin coating. Upon etching of ZnO, TiO{sub 2} nanotubes consisting of 10-15 nm nanoparticles were generated, as confirmed by wide-angle x-ray scattering (WAXS), energy-filtering transmission electron microscopy (EF-TEM) and field-emission scanning electron microscopy (FE-SEM). The ordered and interconnected nanotube architecture showed an enhanced light scattering effect and increased penetration of polymer electrolytes in dye-sensitized solar cells (DSSC). The energy conversion efficiency reached 1.82% for liquid electrolyte, and 1.46% for low molecular weight (M{sub w}) and 0.74% for high M{sub w} polymer electrolytes.

  15. Fabrication and EMI shielding effectiveness of Ag-decorated highly porous poly(vinyl alcohol)/Fe2O3 nanofibrous composites

    International Nuclear Information System (INIS)

    Kim, Hae-Rim; Kim, Byoung-Suhk; Kim, Ick-Soo

    2012-01-01

    The Ag-decorated poly(vinyl alcohol) (PVA) composite nanofibrous webs incorporating Fe 2 O 3 nanoparticles were fabricated by electrospinning and metal-deposition methods for electromagnetic interference (EMI) shielding applications. The Ag-decorated PVA/Fe 2 O 3 composite nanofiber webs with various Ag thicknesses and different amounts of Fe 2 O 3 nanoparticles were prepared and used for EMI shielding measurement. For the EMI SE measurement, a near-field antenna measurement system was used. The measurement of EMI SE was carried out at the frequency range from 0.5 to 18 GHz, and the electromagnetic parameters were measured. The morphologies and microstructures of the resultant PVA/Fe 2 O 3 composite nanofiber webs were characterized using field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM), respectively. The effects of surface morphologies and Fe 2 O 3 nanoparticles on the EMI shielding effectiveness of Ag-decorated PVA/Fe 2 O 3 composite nanofiber webs were investigated. -- Highlights: ► We prepare Ag-decorated poly(vinyl alcohol) nanowebs incorporating Fe 2 O 3 nanoparticles. ► Solvents will affect the fiber morphologies and Fe 2 O 3 nanoparticles dispersion. ► EMI shielding effectiveness depends on the metal thickness and Fe 2 O 3 nanoparticles dispersion.

  16. Photo-triggered release from liposomes without membrane solubilization, based on binding to poly(vinyl alcohol) carrying a malachite green moiety.

    Science.gov (United States)

    Uda, Ryoko M; Kato, Yutaka; Takei, Michiko

    2016-10-01

    When working with liposomes analogous to cell membranes, it is important to develop substrates that can regulate interactions with the liposome surface in response to light. We achieved a photo-triggered release from liposomes by using a copolymer of poly(vinyl alcohol) carrying a malachite green moiety (PVAMG). Although PVAMG is a neutral polymer under dark conditions, it is photoionized upon exposure to UV light, resulting in the formation of a cationic site for binding to liposomes with a negatively charged surface. Under UV irradiation, PVAMG showed effective interaction with liposomes, releasing the encapsulated compound; however, this release was negligible under dark conditions. The poly(vinyl alcohol) moiety of PVAMG played an important role in the photo-triggered release. This release was caused by membrane destabilization without lipid solubilization. We also investigated different aspects of liposome/PVAMG interactions, including PVAMG-induced fusion between the liposomes and the change in the liposome morphologies. Copyright © 2016 Elsevier B.V. All rights reserved.

  17. Effects of Modified Iron Oxide Nanoparticles on the Thermal and Dynamic Mechanical Properties of Cellulose Poly(vinyl alcohol Blend Films

    Directory of Open Access Journals (Sweden)

    Mehdi Roohani

    2015-11-01

    Full Text Available This study was designed to investigate the effect of modified iron oxide nanoparticles (MINP and cellulose nanocrystals (NCC on magnetic, thermal and dynamic-mechanical properties of poly(vinyl alcohol based nanocomposites. Fe3O4 nanoparticles have been synthesized using a chemical co-precipitation route. Nanocomposite films were developed by solvent casting method and their properties were characterized by vibrating sample magnetometer (VSM, differential scanning calorimetry (DSC and dynamic mechanical analysis (DMA. DSC results found that with incorporation of nanoparticles, the glass transition temperature increase slightly to higher temperatures; however, the degree of crystallinity and the values of the melting temperature are found to decrease. Dynamic mechanical analysis revealed that, at the elevated temperatures, improvement of mechanical properties due to the presence of nanoparticles was even more noticeable. Addition of nanoparticles resulted in increased thermal stability of PVA due to the reduction in mobility of matrix molecules by strong hydrogen bonds between nanocomposite components. Results indicated that, MINP and NCC have synergistic effect on improving of poly(vinyl alcohol properties. The VSM findings showed that the saturation magnetization of iron oxide nanoparticles reduced after modification. This can be attributed to formation of hydroxyapatite on nanoparticles surface. The saturation magnetization (Ms of PVA- MINP films was higher than PVA-MINP- NCC film. This result probably is related to more amount of magnetic nanoparticles in PVA-MINP films.

  18. Studies on physical properties and fractography of electron beam irradiated poly(vinyl chloride)/epoxidized natural rubber blend in the presence of trimethylolpropane triacrylate

    International Nuclear Information System (INIS)

    Chantara Thevy Ratnam; Khairul Zaman Mohd Dahlan; Nasir, M.; Baharin, A.

    2000-01-01

    The effect of irradiation on the 50/50 poly(vinyl chloride)/epoxidized natural rubber blend was studied in the presence of 3 phr trimethylolpropane triacrylate (TMPTA). The blend was irradiated by using a 3.0 MeV electron beam machine at doses ranging from 20 to 200 kGy in air and room temperature. The tensile properties, resilience and gel fractions of the blends were measured. Electron beam irradiation of the blend in the presence of the TMPTA were found to cause crosslinking which in effect caused an enhancement in modulus and gel fraction together with a concomitant decline in ultimate elongation. The irradiation has resulted in a less hysteretic poly(vinyl chloride)/epoxidized natural rubber blend, with increased rebound resilience. The tensile strength of the blend reached a maximum at 60 kGy followed by a slight decrease at higher doses, implying embrittlement due to the excessive crosslinking. The scanning electron micrographs of the fracture surfaces of the irradiated blends show evidence consistent with the above contention. (Author)

  19. Fabrication and properties of poly(polyethylene glycol n-alkyl ether vinyl ether)s as polymeric phase change materials

    International Nuclear Information System (INIS)

    Pei, Dong-fang; Chen, Sai; Li, Shu-qin; Shi, Hai-feng; Li, Wei; Li, Xuan; Zhang, Xing-xiang

    2016-01-01

    A series of poly(polyethylene glycol n-alkyl ether vinyl ether)s (PC m E n VEs) with various lengths of alkyl chains and polyethylene glycol spacers as side chain (m = 16,18; n = 1,2) were synthesized via two steps. First, monomers-ethylene glycol hexadecyl ether vinyl ether (C 16 E 1 VE), ethylene glycol octadecyl ether vinyl ether (C 18 E 1 VE), diethylene glycol hexadecyl ether vinyl ether (C 16 E 2 VE) and diethylene glycol octadecyl ether vinyl ether (C 18 E 2 VE) were synthesized by a modified Williamson etherification. Then, four new types of phase change materials were successfully fabricated by a living cationic polymerization. Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance spectroscopy (NMR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and wide-angle X-ray diffraction (WAXD) were employed to characterize their composition, thermal properties and crystallization behavior. The results show that, the side chains of PC 16 E 1 VE, PC 18 E 1 VE, PC 16 E 2 VE and PC 18 E 2 VE are in a hexagonal lattice, and the onset temperatures for melting of PC 16 E 1 VE, PC 18 E 1 VE, PC 16 E 2 VE and PC 18 E 2 VE are 39.8 °C, 37.4 °C, 51.0 °C and 48.9 °C, the onset temperatures for crystallization are 36.7 °C, 35.2 °C, 47.4 °C and 46.3 °C, respectively. The enthalpy changes of PC 18 E 1 VE, PC 16 E 2 VE and PC 18 E 2 VE are higher than 100 J/g; on the contrary, it is 96 J/g for PC 16 E 1 VE. The enthalpy decrease is no more than 11% after 10 heating and cooling cycles. The 5 wt% mass loss temperatures of PC 18 E 1 VE, PC 16 E 2 VE and PC 18 E 2 VE are higher than 300 °C; on the contrary, it’s 283 °C for PC 16 E 1 VE. Using a weak polarity, flexible alkyl ether chain (-OCH 2 CH 2 O-) as a spacer to link the main chain and side chain is conducive to the crystallization of the alkyl side chain. These new phase change materials can be applied in heat storage, energy conservation, and environmental protection.

  20. A fixed cations and low Tg polymer: the poly(4-vinyl-pyridine) quaternized by poly(ethylene oxide) links. Conductivity study; Un electrolyte polymere a cations fixes et bas Tg: les poly(4-vinylpyridine) quaternisees par des chainons de poly(oxyde d`ethylene). Etude de la conductivite

    Energy Technology Data Exchange (ETDEWEB)

    Gramain, Ph. [Ecole Nationale Superieure de Chimie de Montpellier, 34 (France); Frere, Y. [Centre National de la Recherche Scientifique (CNRS), 67 - Strasbourg (France). Institut Charles Sadron

    1996-12-31

    The spontaneous ionic polymerization of 4-vinyl-pyridine in presence of mono-tosylated or bromated short chains of poly(ethylene oxide)-(PEO) is used to prepare amorphous comb-like poly-cations with low Tg. The polymer electrolyte properties of these new structures have been studied without any addition of salts. The ionic conductivity of these fixed cation poly-electrolytes depends on the length of the grafted PEO and varies from 10{sup -7} to 10{sup -4} S/cm between 25 and 80 deg. C. It is only weakly dependent on the nature of the cation but it is controlled by the movements of the pyridinium cation which are facilitated by the plastifying effect of the POE chains which do not directly participate to the ionic transport. (J.S.) 17 refs.

  1. A fixed cations and low Tg polymer: the poly(4-vinyl-pyridine) quaternized by poly(ethylene oxide) links. Conductivity study; Un electrolyte polymere a cations fixes et bas Tg: les poly(4-vinylpyridine) quaternisees par des chainons de poly(oxyde d`ethylene). Etude de la conductivite

    Energy Technology Data Exchange (ETDEWEB)

    Gramain, Ph [Ecole Nationale Superieure de Chimie de Montpellier, 34 (France); Frere, Y [Centre National de la Recherche Scientifique (CNRS), 67 - Strasbourg (France). Institut Charles Sadron

    1997-12-31

    The spontaneous ionic polymerization of 4-vinyl-pyridine in presence of mono-tosylated or bromated short chains of poly(ethylene oxide)-(PEO) is used to prepare amorphous comb-like poly-cations with low Tg. The polymer electrolyte properties of these new structures have been studied without any addition of salts. The ionic conductivity of these fixed cation poly-electrolytes depends on the length of the grafted PEO and varies from 10{sup -7} to 10{sup -4} S/cm between 25 and 80 deg. C. It is only weakly dependent on the nature of the cation but it is controlled by the movements of the pyridinium cation which are facilitated by the plastifying effect of the POE chains which do not directly participate to the ionic transport. (J.S.) 17 refs.

  2. Polysulfone hemodiafiltration membranes with enhanced anti-fouling and hemocompatibility modified by poly(vinyl pyrrolidone) via in situ cross-linked polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Lijing, E-mail: zhulijing@nimte.ac.cn; Song, Haiming; Wang, Jiarong; Xue, Lixin, E-mail: xuelx@nimte.ac.cn

    2017-05-01

    Poly(vinyl pyrrolidone) (PVP) and its copolymers have been widely employed for the modification of hemodiafiltration membranes due to their excellent hydrophilicity, antifouling and hemocompatibility. However, challenges still remain to simplify the modification procedure and to improve the utilization efficiency. In this paper, antifouling and hemocompatibility polysulfone (PSf) hemodiafiltration membranes were fabricated via in situ cross-linked polymerization of vinyl pyrrolidone (VP) and vinyltriethoxysilane (VTEOS) in PSf solutions and non-solvent induced phase separation (NIPS) technique. The prepared membranes were characterized by attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM), which suggested that VP and VTEOS have been cross-linked copolymerized in PSf membranes. The modified PSf membranes with high polymer content showed improved hydrophilicity, ultrafiltration and protein antifouling ability. In addition, the modified PSf membranes showed lower protein adsorption, inhibited platelet adhesion and deformation, prolonged the activated partial thromboplastin time (APTT), prothrombin time (PT), and decreased the content of fibrinogen (FIB) transferring to fibrin, indicating enhanced hemocompatibility. In a word, the present work provides a simple and effective one-step modification method to construct PSf membranes with improved hydrophilicity, antifouling and hemocompatibility. - Highlights: • PSf membranes were modified by in situ cross-linked polymerization. • The modified PSf membranes showed enhanced hydrophilicity. • The anti-fouling and hemocompatibility of PSf membranes were improved.

  3. Hydrogels based on chemically modified poly(vinyl alcohol (PVA-GMA and PVA-GMA/chondroitin sulfate: Preparation and characterization

    Directory of Open Access Journals (Sweden)

    E. C. Muniz

    2012-05-01

    Full Text Available This work reports the preparation of hydrogels based on PVA-GMA, PVA-GMA is poly(vinyl alcohol (PVA functionalized with vinyl groups from glycidyl methacrylate (GMA, and on PVA-GMA with different content of chondroitin sulfate (CS. The degrees of swelling of PVA-GMA and PVA-GMA/CS hydrogels were evaluated in distilled water and the swelling kinetics was performed in simulated gastric and intestinal fluids (SGF and SIF. PVA-GMA and PVAGMA/CS hydrogels demonstrated to be resistant on SGF and SIF fluids. The elastic modulus, E, of swollen-hydrogels were determined through compressive tests and, according to the obtained results, the hydrogels presented good mechanical properties. At last, the presence of CS enhances the hydrogel cell compatibility as gathered by cytotoxicity assays. It was concluded that the hydrogels prepared through this work presented characteristics that allow them to be used as biomaterial, as a carrier in drug delivery system or to act as scaffolds in tissue engineering as well.

  4. In-situ formation of silver nanoparticles on poly (lactic acid) film by γ-radiation induced grafting of N-vinyl pyrrolidone

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Jingxia; Chen, Hao; Chen, Zhuping; Chen, Yuheng; Guo, Dan; Ni, Maojun; Liu, Siyang; Peng, Chaorong, E-mail: pengchaorong_siae@163.com

    2016-06-01

    A fast, easy and novel method for preparing biodegradable polymer films with silver nanoparticles was investigated to endow the material with excellent biocompatibility and antibacterial property. Silver nanoparticles (Ag NPs) were immobilized on the surface of polylactic acid (PLA) film by gamma radiation induced grafting of N-vinyl pyrrolidone (NVP). In this method, poly (N-vinyl pyrrolidone) (PVP) was produced and grafted onto the surface of PLA film by gamma radiation polymerization of NVP. PVP acted as both a bridge to connect the Ag NPs with the PLA film, and a stabilizer to protect the Ag NPs from agglomeration. The effect of various reaction parameters, including NVP/Ag mole ratio and radiation dose, on the fabrication of PLA-g-NVP/Ag film was demonstrated. Moreover, the interaction between PVP and Ag NPs was studied by X-ray photoelectron spectroscopy and Fourier-transform infrared spectroscopy, that revealed the Ag NPs coordinated through the oxygen atom on the carbonyl group of PVP at 15 kGy radiation dose, but through the nitrogen atom and the oxygen atom of the amide group of PVP at 1 kGy dose. - Highlights: • PLA-graft-NVP/Ag film was produced by a simple one-step method. • Ag nanoparticles were immobilized on PLA film by gamma radiation grafting technology. • PVP acted as a bridge to connect Ag nanoparticles and PLA film. • Different content and size of Ag NPs can be reached by varying radiation dose.

  5. Polysulfone hemodiafiltration membranes with enhanced anti-fouling and hemocompatibility modified by poly(vinyl pyrrolidone) via in situ cross-linked polymerization.

    Science.gov (United States)

    Zhu, Lijing; Song, Haiming; Wang, Jiarong; Xue, Lixin

    2017-05-01

    Poly(vinyl pyrrolidone) (PVP) and its copolymers have been widely employed for the modification of hemodiafiltration membranes due to their excellent hydrophilicity, antifouling and hemocompatibility. However, challenges still remain to simplify the modification procedure and to improve the utilization efficiency. In this paper, antifouling and hemocompatibility polysulfone (PSf) hemodiafiltration membranes were fabricated via in situ cross-linked polymerization of vinyl pyrrolidone (VP) and vinyltriethoxysilane (VTEOS) in PSf solutions and non-solvent induced phase separation (NIPS) technique. The prepared membranes were characterized by attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM), which suggested that VP and VTEOS have been cross-linked copolymerized in PSf membranes. The modified PSf membranes with high polymer content showed improved hydrophilicity, ultrafiltration and protein antifouling ability. In addition, the modified PSf membranes showed lower protein adsorption, inhibited platelet adhesion and deformation, prolonged the activated partial thromboplastin time (APTT), prothrombin time (PT), and decreased the content of fibrinogen (FIB) transferring to fibrin, indicating enhanced hemocompatibility. In a word, the present work provides a simple and effective one-step modification method to construct PSf membranes with improved hydrophilicity, antifouling and hemocompatibility. Copyright © 2017 Elsevier B.V. All rights reserved.

  6. Polysulfone hemodiafiltration membranes with enhanced anti-fouling and hemocompatibility modified by poly(vinyl pyrrolidone) via in situ cross-linked polymerization

    International Nuclear Information System (INIS)

    Zhu, Lijing; Song, Haiming; Wang, Jiarong; Xue, Lixin

    2017-01-01

    Poly(vinyl pyrrolidone) (PVP) and its copolymers have been widely employed for the modification of hemodiafiltration membranes due to their excellent hydrophilicity, antifouling and hemocompatibility. However, challenges still remain to simplify the modification procedure and to improve the utilization efficiency. In this paper, antifouling and hemocompatibility polysulfone (PSf) hemodiafiltration membranes were fabricated via in situ cross-linked polymerization of vinyl pyrrolidone (VP) and vinyltriethoxysilane (VTEOS) in PSf solutions and non-solvent induced phase separation (NIPS) technique. The prepared membranes were characterized by attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM), which suggested that VP and VTEOS have been cross-linked copolymerized in PSf membranes. The modified PSf membranes with high polymer content showed improved hydrophilicity, ultrafiltration and protein antifouling ability. In addition, the modified PSf membranes showed lower protein adsorption, inhibited platelet adhesion and deformation, prolonged the activated partial thromboplastin time (APTT), prothrombin time (PT), and decreased the content of fibrinogen (FIB) transferring to fibrin, indicating enhanced hemocompatibility. In a word, the present work provides a simple and effective one-step modification method to construct PSf membranes with improved hydrophilicity, antifouling and hemocompatibility. - Highlights: • PSf membranes were modified by in situ cross-linked polymerization. • The modified PSf membranes showed enhanced hydrophilicity. • The anti-fouling and hemocompatibility of PSf membranes were improved.

  7. In-situ formation of silver nanoparticles on poly (lactic acid) film by γ-radiation induced grafting of N-vinyl pyrrolidone

    International Nuclear Information System (INIS)

    Wang, Jingxia; Chen, Hao; Chen, Zhuping; Chen, Yuheng; Guo, Dan; Ni, Maojun; Liu, Siyang; Peng, Chaorong

    2016-01-01

    A fast, easy and novel method for preparing biodegradable polymer films with silver nanoparticles was investigated to endow the material with excellent biocompatibility and antibacterial property. Silver nanoparticles (Ag NPs) were immobilized on the surface of polylactic acid (PLA) film by gamma radiation induced grafting of N-vinyl pyrrolidone (NVP). In this method, poly (N-vinyl pyrrolidone) (PVP) was produced and grafted onto the surface of PLA film by gamma radiation polymerization of NVP. PVP acted as both a bridge to connect the Ag NPs with the PLA film, and a stabilizer to protect the Ag NPs from agglomeration. The effect of various reaction parameters, including NVP/Ag mole ratio and radiation dose, on the fabrication of PLA-g-NVP/Ag film was demonstrated. Moreover, the interaction between PVP and Ag NPs was studied by X-ray photoelectron spectroscopy and Fourier-transform infrared spectroscopy, that revealed the Ag NPs coordinated through the oxygen atom on the carbonyl group of PVP at 15 kGy radiation dose, but through the nitrogen atom and the oxygen atom of the amide group of PVP at 1 kGy dose. - Highlights: • PLA-graft-NVP/Ag film was produced by a simple one-step method. • Ag nanoparticles were immobilized on PLA film by gamma radiation grafting technology. • PVP acted as a bridge to connect Ag nanoparticles and PLA film. • Different content and size of Ag NPs can be reached by varying radiation dose.

  8. Effects of O2 and H2O plasma immersion ion implantation on surface chemical composition and surface energy of poly vinyl chloride

    International Nuclear Information System (INIS)

    Zhang Wei; Chu, Paul K.; Ji Junhui; Zhang, Yihe; Jiang Zhimin

    2006-01-01

    Oxygen and water plasma immersion ion implantation (PIII) was used to modify poly vinyl chloride (PVC) to enhance oxygen-containing surface functional groups for more effective grafting. The modified surfaces were characterized by X-ray photoelectron spectroscopy (XPS), attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR), and contact angle measurements. Our experimental results show that both oxygen and water PIII can greatly improve the O to C ratios on the surface. The optimal plasma processing conditions differ for the two treatments. The hydrophilicity and surface energy of the plasma-implanted PVC are also improved significantly. Our results indicate that O 2 and H 2 O PIII increase both the polar and dispersion interactions and consequently the surface energy. It can be explained by the large amount of oxygen introduced to the surface and that many C-C bonds are transformed into more polar oxygen containing functional groups

  9. Microwave and ultrasound-assisted synthesis of poly(vinyl chloride)/riboflavin modified MWCNTs: Examination of thermal, mechanical and morphology properties.

    Science.gov (United States)

    Abdolmaleki, Amir; Mallakpour, Shadpour; Azimi, Faezeh

    2018-03-01

    This study focused on the preparation and investigation of physicochemical features of new poly(vinyl chloride) (PVC) nanocomposites (NCs) including different amounts of carboxylated multi-walled carbon nanotubes (MWCNTs-COOH) functionalized with riboflavin (RIB). Firstly, to increase the hydrophilicity of MWCNTs, the surface of them was functionalized by incorporating and formation of ester groups with RIB as a low cost and environmentally friendly biomolecule through ultrasound and microwave irradiations. Afterwards, PVC/RIB-MWCNTs NCs were fabricated via the solution casting and ultrasonic dispersion methods. Prepared NCs were examined by X-ray diffraction, thermogravimetric analysis, field emission scanning electron microscopy, transmission electron micrograph, and Raman spectroscopy. The PVC/RIB-MWCNTs NCs (12wt%) showed the higher mechanical and thermal behavior as compared to other concentration of MWCNTs. Copyright © 2017 Elsevier B.V. All rights reserved.

  10. Effect of crosslinking functionality on microstructure, mechanical properties, and in vitro cytocompatibility of cellulose nanocrystals reinforced poly (vinyl alcohol)/sodium alginate hybrid scaffolds.

    Science.gov (United States)

    Kumar, Anuj; Lee, Yujin; Kim, Doyeon; Rao, Kummara Madhusudana; Kim, Jisoo; Park, Soyoung; Haider, Adnan; Lee, Do Hyun; Han, Sung Soo

    2017-02-01

    Cellulose nanocrystals reinforced poly (vinyl alcohol)/sodium alginate hybrid scaffolds were fabricated by using freeze casting and freeze drying method. In this study, the effect of crosslinking agents such as calcium chloride, orthophosphoric acid, and borax on morphological, structural, thermal, mechanical, and cytocompatibility (cell adhesion and proliferation) properties was investigated. The results showed that the change in type of crosslinking agent significantly changed the properties of the hybrid scaffolds. Based on this study, borax-crosslinked hybrid scaffold showed good fibrous porous structure with high porosity (95.2%), highest water uptake capacity, good thermal stability, mechanical stability (storage modulus), and in vitro cell adhesion and proliferation with fibroblast (NIH3T3) cells. This primarily research study explores the way for further use of this crosslinking agent to design and fabricate scaffolds for tissue engineering applications. Copyright © 2016 Elsevier B.V. All rights reserved.

  11. Study on the performance of eosin-doped poly(vinyl alcohol)/acrylamide photopolymer films for holographic recording using 488-nm wavelength

    Science.gov (United States)

    Rajesh, Chelakkal Sukumaran; Sreeroop, Sasidharan Savithrydevi; Pramitha, Vayalamkuzhi; Joseph, Rani; Sreekumar, Krishnapillai; Kartha, Cheranellore Sudha

    2011-12-01

    This article reports a study done on eosin-doped poly(vinyl alcohol)/acrylamide films for holographic recording using 488 nm Ar+ laser. Films were fabricated using gravity settling method at room temperature and were stored under normal laboratory conditions. Ar+ laser (488 nm) was used for fringe recording. Characterization was done by real time transmittance measurement, optical absorption studies, and diffraction efficiency measurements. Various holographic parameters such as exposure energy, recording power, spatial frequency, etc., were optimized so as to ensure maximum performance. More than 85% diffraction efficiency was obtained at an exposure energy of 50 mJ/cm2 in the optimized film. Efforts were taken to study the environmental stability of this self-developing polymeric material by looking at its shelf life and storage life. Compatibility for recording transmission hologram was also checked.

  12. Poly(N-vinyl-2-pyrrolidone)-stabilized palladium-platinum nanoparticles-catalyzed hydrolysis of ammonia borane for hydrogen generation

    Science.gov (United States)

    Rakap, Murat

    2015-02-01

    The catalytic use of highly efficient poly(N-vinyl-2-pyrrolidone)-stabilized palladium-platinum nanoparticles (4.2 ± 1.9 nm) in the hydrolysis of ammonia-borane is reported. The catalyst is prepared by co-reduction of two metal ions in ethanol/water mixture by an alcohol reduction method and characterized by transmission electron microscopy, X-ray photoelectron spectroscopy and UV-Vis spectroscopy. They are recyclable and highly active for hydrogen generation from the hydrolysis of ammonia-borane even at very low concentrations and temperature, providing a record numbers of average turnover frequency value (125 mol H2/mol cat.min-1) and maximum hydrogen generation rate (3468 L H2 min-1 (mol cat)-1). They also provide activation energy of 51.7 ± 2 kJ/mol for the hydrolysis of ammonia borane.

  13. Electron beam chemistry in solid films of poly(vinyl alcohol): Exposures under vacuum and under N2 at atmospheric pressure; irradiation monitored by using infrared spectroscopy

    International Nuclear Information System (INIS)

    Pacansky, J.; Schneider, S.

    1990-01-01

    Thin films of poly(vinyl alcohol) (PVA) were exposed to a 25-kV electron beam under high vacuum conditions and to a 175-kV electron beam at atmospheric pressures of N 2 . The decomposition of PVA by the electron beam sequentially formed materials that had polyketone- and polyethylene-like structures, respectively. Contrary to previous reports we show that the ketone groups formed as a result of the electron beam exposure are not due to an oxidation step by molecular oxygen. Damage cross sections for the electron beam decomposition (at 25 kV) were determined for PVA and the polyketone, and G values were determined for decomposition of -OH groups and formation of ketone functional groups

  14. Effect of electron beam irradiation on the structural properties of poly(vinyl alcohol) formulations with triphenyl tetrazolium chloride dye (TTC)

    Science.gov (United States)

    Ali, Z. I.; Said, Hossam M.; Ali, H. E.

    2006-01-01

    Films of poly(vinyl alcohol) (PVA) composites with triphenyl tetrazolium chloride (TTC) dye were prepared and exposed to various radiation doses delivered by accelerated electrons. The results showed that at a low dose of 50 kGy, the colour difference (Δ E*) of PVA/TTC films was increased by ˜10 times of the initial value. However, the change in colour differences did not go systematically with increasing the TTC content, in which the composite with 1.5 wt% displayed higher value than that with 3.5 wt%. The differential scanning calorimetry (DSC) showed that the presence of the TTC dye caused a depression in the melting point ( Tm) and heat of fusion (Δ Hf) of the PVA bulk polymer. However, the thermogravimetric analysis (TGA) showed that the presence of the TTC dye improved the thermal stability of PVA. Also, the tensile strength at break of PVA/TTC composites was improved after electron beam irradiation.

  15. The Formation of Polycomplexes of Poly(Methyl Vinyl Ether-Co-Maleic Anhydride and Bovine Serum Albumin in the Presence of Copper Ions

    Directory of Open Access Journals (Sweden)

    Karahan Mesut

    2014-09-01

    Full Text Available The binary and ternary complex formations of poly(methyl vinyl ether-co-maleic anhydride (PMVEMA with copper ions and with bovine serum albumin (BSA in the presence of copper ions in phosphate buffer solution at pH = 7 were examined by the techniques of UV-visible, fluorescence, dynamic light scattering, atomic force microscopy measurements. In the formation of binary complexes of PMVEMA-Cu(II, the addition of copper ions to the solution of PMVEMA in phosphate buffer solution at pH = 7 forms homogeneous solutions when the molar ratio of Cu(II/MVEMA is 0.5. Then the formations of ternary complexes of PMVEMA-Cu(II-BSA were examined. Study analysis revealed that the toxicities of polymer-metal and polymer-metal-protein mixture solutions depend on the nature and ratio of components in mixtures.

  16. Palladium Nanoparticles Immobilized on Poly(vinyl chloride-Supported Pyridinium as an Efficient and Recyclable Catalyst for Suzuki-Miyaura Cross-Coupling Reaction

    Directory of Open Access Journals (Sweden)

    Bo Zhou

    2011-01-01

    Full Text Available The palladium nanoparticles immobilized on the polymeric surface of poly(vinyl chloride-supported pyridinium (PVC-Py-Pd0 were achieved by a simple procedure by applying the corresponding functionalized polymer and palladium chloride in ethanol solution. The as-prepared catalyst (PVC-Py-Pd0 was found to be air and moisture stable and exhibits significant catalytic activity for Suzuki-Miyaura cross-coupling reaction of various aryl halides and phenylboronic acid under milder operating conditions. The procedure presented here showed several merits such as short reaction time, simple experimental and isolated procedure and excellent yields of products. Furthermore, the catalyst can be easily recovered and reused for at least six times with consistent activities.

  17. Ultraviolet and infrared spectral analysis of poly(vinyl)butyral films: correlation and possible application for high-dose radiation dosimetry

    International Nuclear Information System (INIS)

    Ebraheem, S.; El-Kelany, M.; Beshir, W.; Abdel-Fattah, A.A.

    1999-01-01

    A detailed study was performed to develop the dosimetric characteristics of poly(vinyl)butyral film (PVB), to be used as a film dosimeter for high-dose gamma radiation dosimetry. The useful dose range of this polymeric film extends up to 350 kGy. Correlations were established between the absorbed dose of gamma radiation and the radiation-induced changes in PVB measured by means of ultraviolet (UV) and Fourier Transform Infrared (FTIR) spectrophotometry. The results showed a significant dependence of the response on the selected readout tool of measurements whether FTIR (at 1738 and 3400 cm -1 ) or UV (at 275 and 230 nm), as well as on the quantity used for calculation. The effect of relative humidity during irradiation on dosimeter performance as well as the post-irradiation stability at different storage conditions are also discussed. (author)

  18. Effects of Kenaf Loading on Processability and Properties of Linear Low-Density Polyethylene/Poly (Vinyl Alcohol/Kenaf Composites

    Directory of Open Access Journals (Sweden)

    Ai Ling Pang

    2015-09-01

    Full Text Available This study was conducted to evaluate the possibility of utilizing kenaf (KNF in LLDPE/PVOH to develop a new thermoplastic composite. The effect of KNF loading on the processability and mechanical, thermal and water absorption properties of linear low-density polyethylene/poly (vinyl alcohol/kenaf (LLDPE/PVOH/KNF composites were investigated. Composites with different KNF loadings (0, 10, 20, 30, and 40 phr were prepared using a Thermo Haake Polydrive internal mixer at a temperature of 150 °C and rotor speed of 50 rpm for 10 min. The results indicate that the stabilization torque, tensile modulus, water uptake, and thermal stability increased, while tensile strength and elongation at break decreased with increasing filler loading. The tensile fractured surfaces observed by scanning electron microscopy (SEM supported the deterioration in tensile properties of the LLDPE/PVOH/KNF composites with increasing KNF loading.

  19. Effects of Polyethylene Grafted Maleic Anhydride on the Mechanical, Morphological, and Swelling Properties of Poly (Vinyl Chloride / Epoxidized Natural Rubber / Kenaf Core Powder Composites

    Directory of Open Access Journals (Sweden)

    Rohani Abdul Majid

    2014-10-01

    Full Text Available The effects of polyethylene grafted maleic anhydride (PE-g-MA on the properties of poly (vinyl chloride/epoxidized natural rubber (PVC/ENR kenaf core powder composites were studied, with four different loadings of kenaf core powder (5, 10, 15, and 20 phr. The tensile properties indicated that the strength and elongation at break of the composites exhibited an increase for samples with PE-g-MA. Morphological analysis using a scanning electron microscope (SEM showed better dispersion of kenaf fiber with the addition of PE-g-MA and less kenaf powder agglomeration. Furthermore, the swelling index indicated that composites with PE-g-MA showed lower toluene absorption than composites without PE-g-MA.

  20. Fabrication of novel nanofiber scaffolds from gum tragacanth/poly(vinyl alcohol) for wound dressing application: In vitro evaluation and antibacterial properties

    International Nuclear Information System (INIS)

    Ranjbar-Mohammadi, Marziyeh; Bahrami, S. Hajir; Joghataei, M.T.

    2013-01-01

    Gum tragacanth (GT) is one of the most widely used natural gums which has found applications in many areas because of its attractive features such as biodegradability, nontoxic nature, natural availability, higher resistance to microbial attacks and long shelf-life properties. GT and poly(vinyl alcohol) (PVA) were dissolved in deionized water in different ratios i.e., 0/100, 30/70, 60/40, 50/50, 40/60, 70/30, 0/100 mass ratio of GT/PVA. Nanofibers were produced from these solutions using electrospinning technique. The effect of different electrospinning parameters such as extrusion rate of polymer solutions, solution concentration, electrode spacing distance and applied voltage on the morphology of nanofibers was examined. The antibacterial activity of nanofibers and GT solution against Staphylococcus aureus and Pseudomonas aeruginosa was examined and these nanofibers showed good antibacterial property against Gram-negative bacteria. FTIR data showed that these two polymers may be having hydrogen bonding interactions. DSC data revealed that the exothermic peak at about 194 °C for PVA shifted to a lower temperature in GT/PVA blend. Human fibroblast cells adhered and proliferated well on the GT/PVA nanofiber scaffolds. MTT assay was carried out on the GT/PVA nanofiber to investigate the proliferation rate of fibroblast cells on the scaffolds. - Highlights: • Novel biodegradable scaffolds from natural biopolymer gum tragacanth and poly(vinyl alcohol) were successfully fabricated. • Human fibroblast cells adhered and proliferated well on the GT/PVA nanofiber scaffolds. • MTT assay confirmed nanofibers have cell viability property and biological compatibility. • Biocompatibility and antibacterial properties of nanofibers showed that produced nanofibers are effective wound dressing

  1. Preparation and properties of poly(vinyl alcohol/chitosan blend bionanocomposites reinforced with cellulose nanocrystals/ZnO-Ag multifunctional nanosized filler

    Directory of Open Access Journals (Sweden)

    Azizi S

    2014-04-01

    Full Text Available Susan Azizi,1 Mansor Bin Ahmad,1 Mohd Zobir Hussein,1 Nor Azowa Ibrahim,1 Farideh Namvar2,31Department of Chemistry, Faculty of Science, 2Institute of Tropical Forestry and Forest Products, University Putra Malaysia, Selangor, Malaysia; 3Mashhad Branch, Islamic Azad University, Mashhad, IranAbstract: A series of novel bionanocomposites were cast using different contents of zinc oxide-silver nanoparticles (ZnO-AgNPs stabilized by cellulose nanocrystals (CNC as multifunctional nanosized fillers in poly(vinyl alcohol/chitosan (PVA/Cs matrices. The morphological structure, mechanical properties, ultraviolet-visible absorption, and antimicrobial properties of the prepared films were investigated as a function of their CNC/ZnO-AgNP content and compared with PVA/chitosan/CNC bionanocomposite films. X-ray diffraction and field emission scanning electron microscopic analyses showed that the CNC/ZnO-AgNPs were homogeneously dispersed in the PVA/Cs matrix and the crystallinity increased with increasing nanosized filler content. Compared with pure PVA/Cs, the tensile strength and modulus in the films increased from 0.055 to 0.205 GPa and from 0.395 to 1.20 GPa, respectively. Ultraviolet and visible light can be efficiently absorbed by incorporating ZnO-AgNPs into a PVA/Cs matrix, suggesting that these bionanocomposite films show good visibility and ultraviolet-shielding effects. The bionanocomposite films had excellent antimicrobial properties, killing both Gram-negative Salmonella choleraesuis and Gram-positive Staphylococcus aureus. The enhanced physical properties achieved by incorporating CNC/ZnO-AgNPs could be beneficial in various applications.Keywords: multifunctional nanofiller, bionanocomposite, cellulose nanocrystals, antimicrobial properties, poly(vinyl alcohol/chitosan blend

  2. Colorful and transparent poly(vinyl alcohol) composite films filled with layered zinc hydroxide salts, intercalated with anionic orange azo dyes (methyl orange and orange II)

    International Nuclear Information System (INIS)

    Neves da Silva, Marlon Luiz; Marangoni, Rafael; Cursino, Ana Cristina Trindade; Schreiner, Wido Herwig; Wypych, Fernando

    2012-01-01

    Highlights: ► Zinc hydroxide salts were successfully intercalated with anionic orange azo dyes. ► The anionic dye was co-intercalated with hydrated chloride anions. ► The orange materials were used as fillers for poly(vinyl alcohol). ► Transparent, homogeneous, colorful PVA films were obtained by wet casting. ► Some composites stored at lower humidity exhibited improved mechanical properties. - Abstract: Layered zinc hydroxide salts (zinc LHS) were intercalated with anionic orange azo dyes, namely methyl orange (MO) and orange II (OII), and co-intercalated with hydrated chloride anions. After characterization by X-ray diffraction (XRD), thermal analysis (TGA/DTA), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS), the materials were used as fillers for poly(vinyl alcohol) (PVA). Colorful transparent films were obtained by wet casting, revealing good dispersion of the material into the polymer. In the case of zinc LHS/OII, PVA was intercalated between the zinc LHS layers. Evaluation of the mechanical properties of the PVA composite films revealed that the layered colorful materials were able to increase the mechanical properties of the PVA films only when the films were stored under lower relative humidity. As expected, films with higher water content displayed reduced tensile strength and modulus because of the plasticizing effect of water. As for the films stored at 43% relative humidity, more pronounced improvement of modulus was observed for 1 and 4% zinc LHS/OII, and enhanced tensile strength was achieved for 0.5 and 1% zinc LHS/OII. This effect can be attributed to better dispersion of the layered filler and its better adhesion to the PVA matrix.

  3. Fabrication of novel nanofiber scaffolds from gum tragacanth/poly(vinyl alcohol) for wound dressing application: In vitro evaluation and antibacterial properties

    Energy Technology Data Exchange (ETDEWEB)

    Ranjbar-Mohammadi, Marziyeh [Textile Engineering Department, Amirkabir University of Technology, Tehran (Iran, Islamic Republic of); Bahrami, S. Hajir, E-mail: hajirb@yahoo.com [Textile Engineering Department, Amirkabir University of Technology, Tehran (Iran, Islamic Republic of); Joghataei, M.T. [Cellular and Molecular Research Center, Tehran University of Medical Science, Tehran (Iran, Islamic Republic of)

    2013-12-01

    Gum tragacanth (GT) is one of the most widely used natural gums which has found applications in many areas because of its attractive features such as biodegradability, nontoxic nature, natural availability, higher resistance to microbial attacks and long shelf-life properties. GT and poly(vinyl alcohol) (PVA) were dissolved in deionized water in different ratios i.e., 0/100, 30/70, 60/40, 50/50, 40/60, 70/30, 0/100 mass ratio of GT/PVA. Nanofibers were produced from these solutions using electrospinning technique. The effect of different electrospinning parameters such as extrusion rate of polymer solutions, solution concentration, electrode spacing distance and applied voltage on the morphology of nanofibers was examined. The antibacterial activity of nanofibers and GT solution against Staphylococcus aureus and Pseudomonas aeruginosa was examined and these nanofibers showed good antibacterial property against Gram-negative bacteria. FTIR data showed that these two polymers may be having hydrogen bonding interactions. DSC data revealed that the exothermic peak at about 194 °C for PVA shifted to a lower temperature in GT/PVA blend. Human fibroblast cells adhered and proliferated well on the GT/PVA nanofiber scaffolds. MTT assay was carried out on the GT/PVA nanofiber to investigate the proliferation rate of fibroblast cells on the scaffolds. - Highlights: • Novel biodegradable scaffolds from natural biopolymer gum tragacanth and poly(vinyl alcohol) were successfully fabricated. • Human fibroblast cells adhered and proliferated well on the GT/PVA nanofiber scaffolds. • MTT assay confirmed nanofibers have cell viability property and biological compatibility. • Biocompatibility and antibacterial properties of nanofibers showed that produced nanofibers are effective wound dressing.

  4. Surface modification of thermoplastic poly(vinyl alcohol)/saponite nanocomposites via surface-initiated atom transfer radical polymerization enhanced by air dielectric discharges barrier plasma treatment

    International Nuclear Information System (INIS)

    Zhen Weijun; Lu Canhui

    2012-01-01

    To improve the water resistance of thermoplastic poly(vinyl alcohol)/saponite nanocomposites (TPVA), a simple two-step method was developed for the covalent immobilization of atom transfer radical polymerization (ATRP) initiators on the TPVA surfaces enhanced by air dielectric barrier discharges (DBD) plasma treatment, and hydrophobic poly(methyl methacrylate) (PMMA) brushes were then grafted onto the surface of TPVA via surface-initiated atom transfer radical polymerization (SI-ATRP). The chemical composition, morphology and hydrophobicity of the modified TPVA surfaces were characterized by X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM), respectively. The water resistance of the surface-functionalized PMMA was evaluated by the contact angle and water adsorption method. It was shown that air DBD plasma treatment activated the TPVA surface and accelerated the immobilization of ATRP initiator on the TPVA surface. Compared with TPVA control, TPVA modified by SI-ATRP can be grafted well-defined and covalently tethered network PMMA brushes onto the surface and the hydrophobicity of TPVA were significantly enhanced.

  5. Poly(ethylene oxide) surfactant polymers

    OpenAIRE

    VACHEETHASANEE, KATANCHALEE; WANG, SHUWU; QIU, YONGXING; MARCHANT, ROGER E.

    2004-01-01

    We report on a series of structurally well-defined surfactant polymers that undergo surface-induced self-assembly on hydrophobic biomaterial surfaces. The surfactant polymers consist of a poly(vinyl amine) backbone with poly(ethylene oxide) and hexanal pendant groups. The poly(vinyl amine) (PVAm) was synthesized by hydrolysis of poly(N-vinyl formamide) following free radical polymerization of N-vinyl formamide. Hexanal and aldehyde-terminated poly (ethyleneoxide) (PEO) were simultaneously att...

  6. Decreased material-activation of the complement system using low-energy plasma polymerized poly(vinyl pyrrolidone) coatings

    DEFF Research Database (Denmark)

    Andersen, T.E.; Kolmos, H.J.; Palarasah, Yaseelan

    2011-01-01

    In the current study we investigate the activation of blood complement on medical device silicone rubber and present a plasma polymerized vinyl pyrrolidone (ppVP) coating which strongly decreases surface-activation of the blood complement system. We show that uncoated silicone and polystyrene...... surface. The ppVP surface is furthermore characterized physically and chemically using scanning electron microscopy (SEM), x-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR), which indicates preservation of chemical functionality by the applied plasma process. Overall, the pp...

  7. Small Angle Neutron Scattering Studies on Blends of Poly (Styrene-ran-Vinyl Phenol) with Liquid Crystalline Polyurethane

    Science.gov (United States)

    Mehta, Rujul

    2005-03-01

    Molecular composites, composed of uniformly dispersed rigid-rod liquid crystalline polymer (LCP) molecules in a flexible amorphous polymer matrix, have remained hitherto elusive due to a scarcity of miscible systems containing a LCP and an amorphous polymer. The production of such a blend, with an experimentally accessible miscibility window, has become possible by modifying the architecture of the flexible polymer, so as to induce favorable intermolecular hydrogen bonding. Specifically, liquid crystalline polyurethanes (LCPU) are found to be miscible with a copolymer of styrene and vinyl phenol; with optimum hydrogen bonding between the carbonyl groups of the urethane linkages and the hydroxyl groups present in the styrenic matrix. Availability of a truly miscible molecular composite presents a unique opportunity of studying the confirmation of polymer chains containing rigid-rods that are uniformly dispersed in a flexible coil matrix. A system consisting of the LCPU and the deuterated styrenic copolymer containing 20% vinyl phenol is examined by Small Angle Neutron Scattering at the National Center for Neutron Research at Gaithersburg and Technology, and the Institute of Solid State Research (IFF) at Jülich. Scattering curves for neat dPS-VPh did not fit the Debye-Bueche model; indicating complex structure. A two correlation length Debye-Bueche model was considered to accommodate for this nonlinear behavior. This model utilizes four fitting parameters, including two correlation lengths a1 and a2, corresponding to a Debye-Bueche model and Guinier model.

  8. Active film of poly(vinyl chloride)/silver: synthesis, characterization and evaluation as antimicrobial active packaging; Filme ativo de poli(cloreto de vinila)/prata: sintese, caracterizacao e avaliacao como embalagem ativa antimicrobiana

    Energy Technology Data Exchange (ETDEWEB)

    Braga, Lilian R.; Rangel, Ellen T.; Machado, Fabricio, E-mail: lilianrodribraga@gmail.com [Universidade de Brasilia (UnB), Brasilia, DF, (Brazil)

    2015-07-01

    The antimicrobial films based on poly(vinyl chloride) (PVC) mediated silver (1, 2, 4 and 8 wt%) were evaluated as antimicrobial active packaging using the casting method. The structure of the active films was characterized by SEM, EDX-XRF, XRD, FTIR and TG. FTIR spectra confirmed the PVC-Ag interaction due to the presence of new bands at 1745 cm{sup -1} and 1165 cm{sup -1} bands, which are absent in the PVC control. The FRX-EDX spectrum confirmed the presence of silver ions in all the films. TG and SEM results showed that the increased concentration of silver provided an improved thermal stability and presence of pores in the active films, respectively. Antimicrobial activity was evaluated by disk diffusion method for Bacillus subtilis, Fusarium solani and Apergillus niger, which proved the efficiency of the films active. (author)

  9. Synthesis and characterization of particles derived of poly(vinyl alcohol) (PVA) for treatment of embolization and chemoembolization;Sintese e caracterizacao de particulas derivadas de poli(alcool vinilico) (PVA) para embolizacao e quimioembolizacao

    Energy Technology Data Exchange (ETDEWEB)

    Semenzim, Vinicius L.; Basso, Glaucia G.; Passos, Rodrigo A.; Nery, Jose G. [UNESP, Sao Jose do Rio Preto, SP (Brazil); Agreli, Guilherme; Oliveira, Ana P.M.L.; Kawasaki-Oyama, Rosa S.; Braile, Domingo M., E-mail: nery@ibilce.unesp.b [Braile Biomedica Industria e Comercio Representacoes S.A., Sao Jose do Rio Preto, SP (Brazil)

    2009-07-01

    The most effective way to treat cancerous tumors is by surgically removing them. However in some types of cancer, such as liver and uterine cancer, more than two-thirds of patients have no indication for surgery due to the size and location of the tumor, such as into the blood vessels. Doctors and researchers have invested in alternative and less invasive methods such as chemoembolization. The objectives of this research project are the synthesis and characterization of poly(vinyl alcohol) (PVA) particles for use in cancer treatment. PVA particles will be combined with chemotherapeutic agent Doxorubicin, drug commonly used in the treatment of cancers and carcinomas. The particles, obtained by controlled polymerization reaction followed by saponification, were characterized by SEM, XRD and NMR-CP/MAS. The functionalization of the particles with the drug is the next step of this study. (author)

  10. Effect of chitosan content on morphology and thermal properties of poly (vinyl alcohol) / chitosan blends; Eefeito do teor de quitosana na morfologia e propriedades termicas das blendas de poli (alcool vinilico) / quitosana

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Barbara Fernanda F. dos; Silva, Jessica Raquel M.B. da; Leite, Itamara Farias, E-mail: itamaraf@gmail.com [Universidade Federal da Paraiba (UFPB), Joao Pessoa, PB (Brazil). Centro de Tecnologia. Departamento de Engenharia de Materiais

    2015-07-01

    The objective of this work consists in the preparation and characterization of blends consisting of biodegradable polymers, chitosan (CS) and poly (vinyl alcohol) (PVA), to evaluate the effect of different chitosan content in morphology and thermal properties of PVA blends/CS, prepared by the solution method. Therefore, the blends were characterized by Infrared Spectroscopy Fourier Transform (FTIR), X-Ray Diffraction (XRD), Differential Scanning Calorimetry (DSC) and Thermogravimetry (TG). The results showed a good degree of interaction between the polymers of the blend constituents, suggesting certain degree of miscibility in the mixture. It was observed by XRD, that as the chitosan content in the mixture decreases PVA/CS, there is a slight increase in crystallinity. In comparative analysis, is observed that the composition PVA1/CS1 was the composition that showed improvement in thermal stability. (author)

  11. Synthesis and characterization of poly(methyl methacrylate-co-vinyl acetate) and its evaluation as filtrate reducer; Sintese e caracterizacao de poli(metacrilato de metila-co-acetato de vinila) e sua avaliacao como redutor de filtrado

    Energy Technology Data Exchange (ETDEWEB)

    Nunes, Rita de Cassia P.; Pires, Renata V.; Segtovich, Iuri V.; Lucas, Elizabete F. [Universidade Federal do Rio de Janeiro, Instituto de Macromoleculas, Laboratorio de Macromoleculas e Coloides na Industria de Petroleo, (UFRJ), RJ (Brazil)], e-mail: repires@ima.ufrj.br

    2011-07-01

    The drilling of petroleum well is extremely important and requires the use of suitable drilling fluids in order to ensure an efficient operation without causing rock damage. Specific polymers have been used in controlling infiltration during drilling, ensuring the operation success. In this work, spherical microparticles of poly(methyl methacrylate-co-vinyl acetate) (PMMA-VAc), prepared by suspension polymerization, were evaluated in terms of their performance in controlling filtrate loss of aqueous fluids. A filter press test with ceramic disc, simulating the rock, was used. The performance of the synthesized materials was compared to that of commercial polymers. It was observed that the performance of the material is directly associated to the relation between particle size and pore size of rock specimen. Furthermore, when the particle size is suitable, the rubbery characteristic of the material produces a more efficient filter cake, for filtrate control. (author)

  12. Solvent Stability Study with Thermodynamic Analysis and Superior Biocatalytic Activity of Burkholderia cepacia Lipase Immobilized on Biocompatible Hybrid Matrix of Poly(vinyl alcohol) and Hypromellose.

    Science.gov (United States)

    Badgujar, Kirtikumar C; Bhanage, Bhalchandra M

    2014-12-26

    In the present study, we have synthesized a biocompatible hybrid carrier of hypromellose (HY) and poly(vinyl alcohol) (PVA) for immobilization of Burkholderia cepacia lipase (BCL). The immobilized biocatalyst HY:PVA:BCL was subjected to determination of half-life time (τ) and deactivation rate constant (K(D)) in various organic solvents. Biocatalyst showed higher τ-value in a nonpolar solvent like cyclohexane (822 h) as compared to that of a polar solvent such as acetone (347 h), which signifies better compatibility of biocatalyst in the nonpolar solvents. Furthermore, the K(D)-value was found to be less in cyclohexane (0.843 × 10(-3)) as compared to acetone (1.997 × 10(-3)), indicating better stability in the nonpolar solvents. Immobilized-BCL (35 mg) was sufficient to achieve 99% conversion of phenethyl butyrate (natural constituent of essential oils and has wide industrial applications) using phenethyl alcohol (2 mmol) and vinyl butyrate (6 mmol) at 44 °C in 3 h. The activation energy (E(a)) was found to be lower for immobilized-BCL than crude-BCL, indicating better catalytic efficiency of immobilized lipase BCL. The immobilized-BCL reported 6-fold superior biocatalytic activity and 8 times recyclability as compared to crude-BCL. Improved catalytic activity of immobilized enzyme in nonpolar media was also supported by thermodynamic activation parameters such as enthalpy (ΔH(⧧)), entropy (ΔS(⧧)) and Gibb's free energy (ΔG(⧧)) study, which showed that phenethyl butyrate synthesis catalyzed by immobilized-BCL was feasible as compared to crude-BCL. The present work explains a thermodynamic investigation and superior biocatalytic activity for phenethyl butyrate synthesis using biocompatible immobilized HY:PVA:BCL in nonaqueous media for the first time.

  13. ILC (ionic liquid colloids) based on p(4-VP) (poly(4-vinyl pyridine)) microgels: Synthesis, characterization and use in hydrogen production

    International Nuclear Information System (INIS)

    Sahiner, Nurettin; Turhan, Tugce; Lyon, L. Andrew

    2014-01-01

    In this study for the first time p(4-VP) (poly(4-vinyl pyridine)) colloidal ionic liquid particles derived from 4-VP (4-vinyl pyridine) are reported, used in the preparation of a catalyst system by loading metal salts such as CoCl 2 and NiCl 2 from ethyl alcohol solutions into the modified p(4-VP) particles, and used for hydrogen generation from NaOH-free hydrolysis of NaBH 4 . Colloidal ionic liquids containing 0.054 mmol Co and Ni were used in NaOH-free hydrolysis of 0.30 g NaBH 4 in 50 mL water at 40 °C and 1000 rpm mixing rate. The reaction rates relating to hydrolysis of NaBH 4 were 3148 (mL H 2 ) (min) −1 (g of Co) −1 for Co, and 1803 (mL H 2 ) (min) −1 (g of Ni) −1 for Ni. The effect of metal loading time, NaBH 4 concentration, temperature, and kinetic parameters were also investigated. The activation energy, enthalpy, and activation entropy for the reaction of NaBH 4 in the presence of the colloidal dicationic catalyst system were calculated as 43.98 kJ/mol, 40.38 kJ/mol, and −178.22 J/mol.K, respectively. - Highlights: • Microgel Ionic liquid colloid reactors for H 2 production. • P(4-VP) microgel ILC (ionic liquid colloid). • Modified microgel for green energy. • Ionic liquid microgel embedding metals salts NaBH 4 hydrolysis. • Ionic liquid microgel catalyst systems

  14. Photo-Fries rearrangements of 1-naphthyl (R-2-phenylpropanoate in poly(vinyl acetate and ethyl acetate: influence of medium polarity and polymer relaxation on motions of singlet radical pairs

    Directory of Open Access Journals (Sweden)

    Xu Jinqi

    2006-01-01

    Full Text Available Both the regio- and stereo-chemistries of the photoreactions of 1-naphthyl (R-2-phenylpropanoate have been investigated in poly(vinyl acetate films in their glassy (at 5masculineC and melted (at 50masculineC states and in ethyl acetate. These results are compared with those from irradiations in polyethylene films and in n-hexane. The regioselectivity of the intermediate 1-naphthoxy/(R-2-phenylpropanoyl radical pair combinations is much higher in both the melt and glassy states of poly(vinyl acetate films than that in the melt state of completely amorphous polyethylene films, but the stereoselectivity of intermediate prochiral 1-naphthoxy/1-phenylethyl radical pair combinations is much lower in poly(vinyl acetate. The results emphasize the need to control the ratio between the rates of radical tumbling and translation, as well as the ratio between the rates of in-cage motions and cage-escape, if high stereo- and regio-selectivities of combination products are to be achieved. A mechanistic picture of how the radicals of the intermediate pairs are affected by and interact with the various media is advanced.

  15. In situ generation of silver nanoparticles in poly(vinyl alcohol)/poly(acrylic acid) polymer membranes in the absence of reducing agent and their effect on pervaporation of a water/acetic acid mixture

    Energy Technology Data Exchange (ETDEWEB)

    Chaudhard, Shvshankar; Kwon, Yong Sung; Moon, MyungJun; Shon, Min Young [Dept. of Industrial Chemistry, Pukyong National University, Busan (Korea, Republic of); Park, You In; Nam, Seung Eun [Center for membranes, Korea Research Institute of Chemical Technology, Daejeon (Korea, Republic of)

    2016-12-15

    The in situ generation of silver nanoparticles in a poly(vinyl alcohol)/poly(acrylic acid) (PVA/PAA) polymer matrix in the absence of any additional reducing agent is reported and tends to the membrane fabrication using solution-casting. Its effect on the separation of a water/acetic acid mixture by pervaporation is described. The results of UV spectroscopy, scanning electron microscopy, and scanning electron microscopy/energy-dispersive X-ray spectroscopy analyses showed that the silver nanoparticles were successfully prepared and well dispersed in the polymer matrix. The increased hydrophilicity of the PVA/PAA membrane due to the presence of silver nanoparticles was confirmed by Fourier transform infrared spectroscopy, contact angle measurements, and membrane absorption studies. Pervaporation data for composite membranes showed a three-fold increase in the flux value, while the initially decreased separation factor subsequently showed a constant value. Overall, the pervaporation data suggested that the presence of silver nanoparticles benefited the dehydration process.

  16. In situ generation of silver nanoparticles in poly(vinyl alcohol)/poly(acrylic acid) polymer membranes in the absence of reducing agent and their effect on pervaporation of a water/acetic acid mixture

    International Nuclear Information System (INIS)

    Chaudhard, Shvshankar; Kwon, Yong Sung; Moon, MyungJun; Shon, Min Young; Park, You In; Nam, Seung Eun

    2016-01-01

    The in situ generation of silver nanoparticles in a poly(vinyl alcohol)/poly(acrylic acid) (PVA/PAA) polymer matrix in the absence of any additional reducing agent is reported and tends to the membrane fabrication using solution-casting. Its effect on the separation of a water/acetic acid mixture by pervaporation is described. The results of UV spectroscopy, scanning electron microscopy, and scanning electron microscopy/energy-dispersive X-ray spectroscopy analyses showed that the silver nanoparticles were successfully prepared and well dispersed in the polymer matrix. The increased hydrophilicity of the PVA/PAA membrane due to the presence of silver nanoparticles was confirmed by Fourier transform infrared spectroscopy, contact angle measurements, and membrane absorption studies. Pervaporation data for composite membranes showed a three-fold increase in the flux value, while the initially decreased separation factor subsequently showed a constant value. Overall, the pervaporation data suggested that the presence of silver nanoparticles benefited the dehydration process

  17. Water-stable diblock polystyrene-block-poly(2-vinyl pyridine) and diblock polystyrene-block-poly(methyl methacrylate) cylindrical patterned surfaces inhibit settlement of zoospores of the green alga Ulva.

    Science.gov (United States)

    Grozea, Claudia M; Gunari, Nikhil; Finlay, John A; Grozea, Daniel; Callow, Maureen E; Callow, James A; Lu, Zheng-Hong; Walker, Gilbert C

    2009-04-13

    Nanopatterned surfaces with hydrophobic and hydrophilic domains were produced using the diblock copolymer polystyrene-block-poly(2-vinyl pyridine) (PS-b-P2VP) and polystyrene-block-poly(methyl methacrylate) (PS-b-PMMA). The PS-b-P2VP diblock copolymer, mixed with the cross-linker benzophenone and spin-coated onto silicon wafers, showed self-assembled cylindrical structures, which were retained after UV treatment for cross-linking. The thin films displayed cylindrical domains after immersion in water. This study shows that pattern retention in water is possible for a long period of time, at least for two weeks in pure water and three weeks in artificial seawater. The PS-b-PMMA diblock showed self-assembled cylindrical structures. PS-b-P2VP and PS-b-PMMA cylindrical patterned surfaces showed reduced settlement of zoospores of the green alga Ulva compared to unpatterned surfaces. The copolymers were investigated using atomic force microscopy and X-ray photoelectron spectroscopy.

  18. Poly(vinyl chloride)-g-poly(2-(dimethylamino)ethyl methacrylate) graft copolymers templated synthesis of mesoporous TiO{sub 2} thin films for dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Patel, Rajkumar; Ahn, Sung Hoon; Seo, Jin Ah; Kim, Sang Jin; Kim, Jong Hak, E-mail: jonghak@yonsei.ac.kr [Yonsei University, Department of Chemical and Biomolecular Engineering (Korea, Republic of)

    2012-07-15

    A poly(vinyl chloride) (PVC) main chain was grafted with poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) containing a quaternary amine group using atom transfer radical polymerization. The successful synthesis of a PVC-g-PDMAEMA graft copolymer was confirmed by Fourier transform infrared, nuclear magnetic resonance, thermogravimetric analysis, and transmission electron microscopy. The PVC-g-PDMAEMA graft copolymer was used as a structure-directing agent (SDA) for the fabrication of a mesoporous thin film containing a titanium dioxide (TiO{sub 2}) layer. To control the porosity of the resultant inorganic layer, the ratio of SDA to TTIP as well as the concentration of the sol-gel was varied. The structure and porosity of the mesoporous film were characterized by XRD and SEM analysis. The mesoporous TiO{sub 2} film fabricated on the FTO surface was used as a photoanode for the dye-sensitized solar cell (DSSC). DSSC performance was the greatest when using TiO{sub 2} film with a higher porosity and lower interfacial resistance. The highest energy conversion efficiency reached 3.2 % at 100 mW/cm{sup 2}, which was one of the highest reported values for a quasi-solid-state DSSC with 600-nm-thick TiO{sub 2} film.

  19. Polyurethanes Crosslinked with Poly(vinyl alcohol as a Slowly-Degradable and Hydrophilic Materials of Potential Use in Regenerative Medicine

    Directory of Open Access Journals (Sweden)

    Justyna Kucińska-Lipka

    2018-02-01

    Full Text Available Novel, slowly-degradable and hydrophilic materials with proper mechanical properties and surface characteristics are in great demand within the biomedical field. In this paper, the design, synthesis, and characterization of polyurethanes (PUR crosslinked with poly(vinyl alcohol (PVA as a new proposition for regenerative medicine is described. PVA-crosslinked PURs were synthesized by a two-step polymerization performed in a solvent (dimethylsulfoxide, DMSO. The raw materials used for the synthesis of PVA-crosslinked PURs were poly(ε-caprolactone (PCL, 1,6-hexamethylene diisocyanate (HDI, and PVA as a crosslinking agent. The obtained materials were studied towards their physicochemical, mechanical, and biological performance. The tests revealed contact angle of the materials surface between 38–47° and tensile strength in the range of 41–52 MPa. Mechanical characteristics of the obtained PURs was close to the characteristics of native human bone such as the cortical bone (TSb = 51–151 MPa or the cancellous bone (TSb = 10–20 MPa. The obtained PVA-crosslinked PURs did not show significant progress of degradation after 3 months of incubation in a phosphate-buffered saline (PBS. Accordingly, the obtained materials may behave similar to slowly-degradable materials, which can provide long-term physical support in, for example, tissue regeneration, as well as providing a uniform calcium deposition on the material surface, which may influence, for example, bone restoration. A performed short-term hemocompatibility study showed that obtained PVA-crosslinked PURs do not significantly influence blood components, and a cytotoxicity test performed with the use of MG 63 cell line revealed the great cytocompatibility of the obtained materials. According to the performed studies, such PVA-crosslinked PURs may be a suitable proposition for the field of tissue engineering in regenerative medicine.

  20. Optimization of the thickness of a conducting polymer, polyaniline, deposited on the surface of poly(vinyl chloride) membranes: a new way to improve their potentiometric response.

    Science.gov (United States)

    Shishkanova, T V; Matejka, P; Král, V; Sedenková, I; Trchová, M; Stejskal, J

    2008-08-29

    Repeated depositions of polyaniline (PANI) have been used to control the thickness of the polymeric film deposited on poly(vinyl chloride) (PVC) membrane surface. The oxidation of aniline was carried out in a dispersion mode, i.e. in the presence of poly(N-vinylpyrrolidone) (PVP). Two kinds of PVC were used for this purpose: a non-plasticized PVC for the study of PANI deposition and PVC, plasticized with nitrophenyl octyl ether (NPOE), as a prototype of a liquid membrane electrode. The results of UV-visible and FTIR spectroscopies and electron microscopy showed that (1) the film thickness increased by about equal increments of approximately 40 nm after each polymerization, and (2) the interface with PVC was constituted by PANI film and adhering PANI-PVP colloidal particles. The various thicknesses of the deposited PANI films affected the potentiometric response of the NPOE/PVC membrane with and without an anion-exchanger. The potentiometric anionic response was observed with a minimal thickness of PANI film on the blank NPOE/PVC membrane. Sensitivity of the PANI film to pH occurred only with a blank NPOE/PVC membrane coated with a thick polymeric film, while it was strongly suppressed by the presence of a lipophilic anion-exchanger, tridodecylmethylammonium chloride (TDDMACl), in the membrane, regardless of the thickness of the polymer film. The thickness of the PANI film did not affect the anionic selectivity pattern of TDDMACl-based membranes to any great extent, but its presence improved and stabilized their potentiometric characteristics (sensitivity, linear-response range).