Science.gov

Sample records for polyvinyl acetate pvac

  1. Twinkling Fractal Analysis of PolyVinyl Acetate (PVAc)

    NASA Astrophysics Data System (ADS)

    Zhang, Yutao; Wool, Richard P.

    2014-03-01

    In amorphous polystyrene melts we have shown by Atomic Force Microscopy (Height and Phase) that dynamic rigid fractal clusters form in equilibrium with the fractal liquid and their relaxation behavior determines the kinetic nature of Tg [J. Non Cryst Solids 357(2): 311-319 2011]. The fractal clusters of size R ~ 1-100 nm have relaxation times ? ~ R1.8 (solid-to-liquid) where the exponent is related to the Fractal dimension Df and Fracton dimension df via Df/df = 1.8. Israeloff et al (2006) showed nanoscale spatio-temporal thermo fluctuations in PVAc using a non-contact Dielectric Force Microscopy technique; PVAC shows similar dynamic clustering using both phase and height tapping AFM modes. The dynamic clusters are clearly evident in the range 1-700 nm. The cluster relaxation behavior was explored in both height and phase modes and found to be different. The fractal clusters have a TFT vibrational density of states G(w) ~ wdf-1 with eigenvalues (frequencies) and eigenvectors (displacements) and these are expected to manifest differently in these AFM studies on PVAc thin films. We examine the cluster relaxation functions C(t) ~ t- 4 / 3 predicted by the TFT and look for the presence of highly mobile layers near surfaces and holes in nanothin films. These results are in accord with computer simulations of anharmonically interacting particles and the recent observation of ``Dancing Molecules'' in strained ceramic glass (Huang et al, Science Oct 2013), as predicted by the TFT.

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

    EPA Science Inventory

    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 ...

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

    PubMed

    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. PMID:21848256

  4. Synthesis of poly(vinyl acetate-methyl methacrylate) copolymer microspheres using suspension polymerization.

    PubMed

    Islam, Md Shahidul; Yeum, Jeong Hyun; Das, Ajoy Kumar

    2012-02-15

    Poly(vinyl acetate-methyl methacrylate) (VAc-MMA) copolymer microspheres were prepared using suspension polymerization at low temperature initiated with 2,2'-azobis(2,4-dimethyl valeronitrile) (ADMVN). The poly(VAc-MMA) copolymer microspheres can be used over a large area where homopolymers, polyvinyl acetate (PVAc) and methyl methacrylate (PMMA) microspheres are capable of being put to use. The prepared microspheres were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA). Obtained copolymer microspheres which have 200 ?m average diameter and higher thermal stability than those of homopolymer. PMID:22137854

  5. Photochemical degradation study of polyvinyl acetate paints used in artworks by Py-GC/MS.

    PubMed

    Wei, Shuya; Pintus, Valentina; Schreiner, Manfred

    2012-09-01

    Photochemical degradation of commercial polyvinyl acetate (PVAc) homopolymer and PVAc paints mixed with burnt umber, cobalt blue, cadmium red dark, nickel azo yellow and titanium white commonly used for artworks were studied by pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) and Fourier transform infrared spectroscopy-attenuated total reflectance (FTIR-ATR). Py-GC/MS with single-shot technique was used for the characterization of the thermal degradation of PVAc at different temperatures, while the double-shot technique of Py-GC/MS was used to reveal the differences in the specimens before and after UV ageing, including the changes of detectable amounts of deacetylation product - acetic acid and plasticizers such as diethyl phthalate (DEP). Furthermore, the relative concentration of the pyrolysis products of the paint samples could be measured and compared in the second step of the double-shot Py-GC/MS, which are highly dependent on the presence of pigments and the ageing status of PVAc paints. PMID:23024446

  6. Method development for compositional analysis of low molecular weight poly(vinyl acetate) by matrix-assisted/laser desorption-mass spectrometry and its application to analysis of chewing gum.

    PubMed

    Tisdale, Evgenia; Wilkins, Charles

    2014-04-11

    The influence of the sample preparation parameters (the choice of the solvent and of the matrix:analyte ratio) was investigated and optimal conditions were established for MALDI mass spectrometry analysis of the pristine low molecular weight polyvinyl acetate (PVAc). It was demonstrated that comparison of polymer's and solvent's Hansen solubility parameters could be used as a guide when choosing the solvent for MALDI sample preparation. The highest intensity PVAc signals were obtained when ethyl acetate was used as a solvent along with the lowest matrix-analyte ratio (2,5-dihydroxybenzoic acid was used as a matrix in all experiments). The structure of the PVAc was established with high accuracy using the matrix-assisted laser desorption/ionization-Fourier transform mass spectrometry (MALDI-FTMS) analysis. It was demonstrated that PVAc undergoes unimolecular decomposition by losing acetic acid molecules from its backbone under the conditions of FTMS measurements. Number and weight average molecular weights as well as polydispersity indices were determined with both MALDI-TOF and MALDI-FTMS methods. The sample preparation protocol developed was applied to the analysis of a chewing gum and the molecular weight and structure of the polyvinyl acetate present in the sample were established. Thus, it was shown that optimized MALDI mass spectrometry could be used successfully for characterization of polyvinyl acetate in commercially available chewing gum. PMID:24745742

  7. Structural and mechanical properties of "peelable" organoaqueous dispersions with partially hydrolyzed poly(vinyl acetate)-borate networks: applications to cleaning painted surfaces.

    PubMed

    Natali, Irene; Carretti, Emiliano; Angelova, Lora; Baglioni, Piero; Weiss, Richard G; Dei, Luigi

    2011-11-01

    The preparation and structural characterization of a family of viscoelastic dispersions of borate cross-linked, 80% hydrolyzed poly(vinyl acetate) (80PVAc) in aqueous-organic liquids are presented. Correlations between mechanical properties (from rheological measurements) and the degree and nature of cross-linking (from (11)B NMR spectroscopy) are reported, and the results are used to assess their potential as low-impact cleaning agents for the surfaces of paintings. Because the dispersions can be prepared at room temperature by simple procedures from readily available materials and can contain up to 50% (w/w) of an organic liquid, they offer important advantages over previously described cleaning agents that are based on fully hydrolyzed PVAc (i.e., poly(vinyl alcohol). The mechanical properties of the various aqueous-organic dispersions, as determined quantitatively by rheological investigations and qualitatively by their ease of removal from a solid surface (i.e., the so-called "peel-off" ability) have been tuned systematically by varying the amount of organic liquid, its structure, and the concentrations of borax and 80PVAc. The (11)B NMR studies demonstrate that the concentration of borate ions actively participating in cross-linking increases significantly with the amount of organic liquid in the mixture. The degree of cross-linking remains constant when the 80PVAc and borax concentrations are varied, as long as their ratios are kept constant. Some of the 80PVAc-borax dispersions have been tested successfully as cleaning agents on the surface of a 16th-17th century oil-on-wood painting by Lodovico Cardi, "Il Cigoli", that was covered by a brown patina and on the surface of a Renaissance wall painting by Vecchietta in Santa Maria della Scala, Siena, Italy, that had a degraded polyacrylate coating from a previous conservation treatment. PMID:21749078

  8. A novel simple one-step air jet spinning approach for deposition of poly(vinyl acetate)/hydroxyapatite composite nanofibers on Ti implants.

    PubMed

    Abdal-Hay, Abdalla; Hamdy, Abdel Salam; Khalil, Khalil Abdelrazek; Lim, Ju Hyun

    2015-04-01

    A biocompatible coating consists of a poly(vinyl acetate)/hydroxyapatite (PVAc/HA) composite nanofiber mat was applied to NaOH-treated titanium metal by means of a novel, facile and efficient air jet spinning (AJS) approach. Results showed that HA nanoparticles (NPs) strongly embedded onto the AJS single fiber surface resulting in a strong chemical interfacial bonding between the two phases due to the difference in kinetic energies. It was proven that AJS membrane coatings can provide significant improvement in the corrosion resistance of titanium substrate. Interestingly, the biocompatibility using MC3T3-E1 osteoblast to the PVAc/HA fiber composite layer coated on Ti was significantly higher than pure titanium-substrates. PMID:25686997

  9. Electro-optical properties of one pot synthesized polyindole in the presence of poly(vinyl acetate)

    NASA Astrophysics Data System (ADS)

    Bhagat, D. J.; Dhokane, G. R.

    2015-05-01

    Polyindole was prepared in the presence of poly(vinyl acetate) through a chemical polymerization technique. The indole monomer was polymerized using ferric chloride as an oxidant. Electrical conductivity measurements were performed through a two probe technique. The prepared composites were analyzed by x-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), field-emission scanning electron microscopy (FE-SEM), energy dispersive x-ray spectroscopy (EDAX), and ultraviolet-visible (UV-VIS) spectroscopy. The DC conductivity was found to be 4.46 × 10-6 S/cm at 383 K. An attempt has been made to investigate the electrooptical properties of PIN/PVAc composite films.[Figure not available: see fulltext.

  10. Strong Surface Treatment Effects on Reinforcement Efficiency in Biocomposites Based on Cellulose Nanocrystals in Poly(vinyl acetate) Matrix.

    PubMed

    Ansari, Farhan; Salajková, Michaela; Zhou, Qi; Berglund, Lars A

    2015-12-14

    In this work, the problem to disperse cellulose nanocrystals (CNC) in hydrophobic polymer matrices has been addressed through application of an environmentally friendly chemical modification approach inspired by clay chemistry. The objective is to compare the effects of unmodified CNC and modified CNC (modCNC) reinforcement, where degree of CNC dispersion is of interest. Hydrophobic functionalization made it possible to disperse wood-based modCNC in organic solvent and cast well-dispersed nanocomposite films of poly(vinyl acetate) (PVAc) with 1-20 wt % CNC. Composite films were studied by infrared spectroscopy (FT-IR), UV-vis spectroscopy, dynamic mechanical thermal analysis (DMTA), tensile testing, and field-emission scanning electron microscopy (FE-SEM). Strongly increased mechanical properties were observed for modCNC nanocomposites. The reinforcement efficiency was much lower in unmodified CNC composites, and specific mechanisms causing the differences are discussed. PMID:26505077

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

    PubMed Central

    Jannesari, Marziyeh; Varshosaz, Jaleh; Morshed, Mohammad; Zamani, Maedeh

    2011-01-01

    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. PMID:21720511

  12. Exploration of CO2-Philicity of Poly(vinyl acetate-co-alkyl vinyl ether) through Molecular Modeling and Dissolution Behavior Measurement.

    PubMed

    Hu, Dongdong; Sun, Shaojun; Yuan, Pei-Qing; Zhao, Ling; Liu, Tao

    2015-09-24

    Hydrocarbon CO2-philes are of great interest for use in expanding CO2 applications as a green solvent. In this work, multiscale molecular modeling and dissolution behavior measurement were both applied to explore CO2-philicity of the poly(vinyl acetate) (PVAc)-based copolymer. Introduction of a favorable comonomer, i.e., vinyl ethyl ether (VEE), could significantly reduce the polymer-polymer interaction on the premise that the polymer-CO2 interaction was not weakened but enhanced. The ab initio calculated interaction of the model molecules with CO2 demonstrated that the ether group in VEE or VBE was the suitable CO2-philic segment. From the molecular dynamics (MD) simulations of polymer/CO2 systems, the interaction energy and Flory-Huggins parameter (?12) of poly(VAc-alt-VEE)/CO2 supported that poly(VAc-alt-VEE) possessed better CO2-philicity than PVAc. The dissolution behaviors of the synthesized poly(VAc-co-alkyl vinyl ether) copolymers in CO2 showed the best CO2-phile had the VEE content of about 34 mol %. The MD simulations also indicated that the interaction of random poly(VAc-co-VEE) containing about 30 mol % VEE with CO2 was the strongest and the ?12 was the smallest in these polymer/CO2 systems. Not only could the VEE monomer reduce the polymer-polymer interaction, but it could also enhance the polymer-CO2 interaction with an optimized composition. Introducing a suitable comonomer with a certain composition might be a promising strategy to form the synergistic effect of polymer-polymer interaction and polymer-CO2 interaction for screening the hydrocarbon CO2-philes. PMID:26332013

  13. Solid As A Rock: The Utilization of Polyvinyl Acetate to Stabilize and Consolidate Museum Sandstone Objects

    E-print Network

    Rock, Chris

    Solid As A Rock: The Utilization of Polyvinyl Acetate to Stabilize and Consolidate Museum Sandstone these objects unstable. Sandstone is a porous rock. The heat treatment and weathering drives off water and makes stabilization treatments that would both increase the density of the rock as well as preserve it from further

  14. Li ion conducting gel polymer electrolytes based on Poly(vinyl acetate)

    NASA Astrophysics Data System (ADS)

    Rajendran, S.; Mathew, Chithra M.; Marimuthu, T.; Kesavan, K.

    2013-06-01

    A novel gel polymer electrolyte based on poly(vinyl acetate) and poly(vinylidene fluoride) with different plasticizers was prepared and studied by X-ray diffraction and Ac impedance methods. The blend polymer electrolyte containing propylene carbonate (PC) exhibits the highest conductivity 0.922 × 10-2 Scm-1 at room temperature and the results were discussed.

  15. Effect of composite microstructure on electrical and mechanical properties of poly(vinyl acetate) composites with carbon black and clay. 

    E-print Network

    Miriyala, Sethu M.

    2009-05-15

    The electrical and mechanical behavior of carbon black filled poly(vinyl acetate) latex-based and solution-based polymer composites was examined. A set of experiments were performed to distinguish composites with a segregated network (emulsion...

  16. Evaluation of the Antimicrobial Effect of Chitosan/Polyvinyl Alcohol Electrospun Nanofibers Containing Mafenide Acetate

    PubMed Central

    Abbaspour, Mohammadreza; Sharif Makhmalzadeh, Behzad; Rezaee, Behjat; Shoja, Saeed; Ahangari, Zohreh

    2015-01-01

    Background: Chitosan, an important biodegradable and biocompatible polymer, has demonstrated wound-healing and antimicrobial properties. Objectives: This study aimed to evaluate the antimicrobial properties of mafenide acetate-loaded nanofibrous films, prepared by the electrospinning technique, using chitosan and polyvinyl alcohol (PVA). Materials and Methods: A 32 full factorial design was used for formulating electrospinning solutions. The chitosan percentage in chitosan/PVA solutions (0%, 10%, and 30%) and the drug content (0%, 20%, and 40%) were chosen as independent variables. The release rate of mafenide acetate from nanofibrous films and their microbial penetration were evaluated. The antimicrobial activity of different nanofibrous film formulations against Staphylococcus aureus and Pseudomonas aeruginosa was studied. Results: The results indicated that all nanofibrous films, with and without drug, can prevent bacterial penetration. Incorporation of mafenide acetate into chitosan/PVA nanofibers enhanced their antimicrobial activity against P. aeruginosa and S. aureus. Conclusions: Overall, the results showed that chitosan/polyvinyl alcohol (PVA) nanofibrous films are applicable for use as a wound dressing with protective, healing, and antimicrobial effects. PMID:26587214

  17. Vibrational and configurational heat capacity of poly(vinyl acetate) from dynamic measurements

    NASA Astrophysics Data System (ADS)

    Tombari, E.; Ziparo, C.; Salvetti, G.; Johari, G. P.

    2007-07-01

    The complex heat capacity Cp* of poly(vinyl acetate) has been measured at 20.95mrad/s modulation frequency during the cooling as well as on heating at 24, 8, and 2K/h and during cooling at 0.5K/h. The study is complemented with (the rate-dependent) Cp,app measured during cooling and heating at 60, 24, and 8K/h. At low temperatures, the real component of Cp* yields the unrelaxed Cp or Cp,vib, the vibrational part of Cp. It is found to be indistinguishable from Cp,glass and lies on a line extrapolated to its equilibrium melt's temperature. At T near Tg,?Cp(=Cp,melt-Cp,glass) shows no detectable contribution from Cp,vib. The finding conflicts with a modified entropy theory calculation [E. A. DiMarzio and F. Dowell, J. Appl. Phys. 50, 6061 (1979)], which had predicted that ˜27% of ?Cp of poly(vinyl acetate) at T near Tg is vibrational in origin and the remainder configurational. At T

  18. Vibrational and configurational heat capacity of poly(vinyl acetate) from dynamic measurements.

    PubMed

    Tombari, E; Ziparo, C; Salvetti, G; Johari, G P

    2007-07-01

    The complex heat capacity C(p) (*) of poly(vinyl acetate) has been measured at 20.95 mrads modulation frequency during the cooling as well as on heating at 24, 8, and 2 Kh and during cooling at 0.5 Kh. The study is complemented with (the rate-dependent) C(p,app) measured during cooling and heating at 60, 24, and 8 Kh. At low temperatures, the real component of C(p) (*) yields the unrelaxed C(p) or C(p,vib), the vibrational part of C(p). It is found to be indistinguishable from C(p,glass) and lies on a line extrapolated to its equilibrium melt's temperature. At T near T(g),DeltaC(p)(=C(p,melt)-C(p,glass)) shows no detectable contribution from C(p,vib). The finding conflicts with a modified entropy theory calculation [E. A. DiMarzio and F. Dowell, J. Appl. Phys. 50, 6061 (1979)], which had predicted that approximately 27% of DeltaC(p) of poly(vinyl acetate) at T near T(g) is vibrational in origin and the remainder configurational. At T

  19. Effect of Hydroxyl Concentration on Chemical Sensitivity of Polyvinyl Alcohol/Carbon-Black Composite Chemiresistors

    SciTech Connect

    Hughes, Robert C.; Patel, Sanjay V.; Yelton, W. Graham

    1999-05-19

    The sensitivity and selectivity of polyvinyl alcohol (PVA) / carbon black composite films have been found to vary depending upon the hydroxylation percentage ("-OH") of the polymer. These chemiresistors made from PVA films whose polymer backbone is 88% hydroxylated (PVA88) have a high sensitivity to water, while chemiresistors made from PVA75 have a higher sensitivity to methanol. The minor differences in polymer composition result in films with different Hildebrand volubility parameters. The relative responses of several different PVA-based chemiresistors to solvents with different volubility parameters are presented. In addition, polyvinyl acetate (PVAC) films with PVA88 are used in an array to distinguish the responses to methanol-water mixtures.

  20. Biomedical applications of stereoregular poly(vinyl alcohol) micro- and nanoparticles

    NASA Astrophysics Data System (ADS)

    Lyoo, Won Seok; Kim, Joon Ho; Kim, Sam Soo; Ghim, Han Do

    2002-11-01

    Syndiotactic poly(vinyl alcohol) (PVA)/poly(vinyl pivalate/vinyl acetate) (P(VPi/VAc)) and atactic PVA/PVAc micro- and nanoparticles with skin/core structure have been prepared by heterogeneous saponification of P(VPi/VAc) and PVAc micro- and nanoparticles. Especially, to prepare P(VPi/VAc) and PVAc microparticles having various particle sizes and uniform particle size distribution, vinyl pivalate (VPi)/vinyl acetate (VAc) and VAc were suspension-polymerized using a low-temperature initiator, 2,2"-azobis(2,4-dimethylvaleronitrile). P(VPi/VAc) particles are promising precursor of stereoregular PVA embolic materials which can be introduced through catheters in the management of gastrointestinal bleeders, arteriovenous malformations, hemangiomas, and traumatic rupture of blood vessels. Monodisperse and/or nearly monodisperse P(VPi/VAc) and PVAc microparticles with various particle diameters were obtained by controlling suspension polymerization conditions. Monodisperse P(VPi/VAc) and PVAc microparticles having various particle sizes were partially saponified in the heterogeneous system. PVA/P(VPi/VAc) and PVA/PVAc microparticles having various tacticity and degree of saponification were produced by controlling various polymerization and saponification conditions. The coating of stereoregular PVA micro- and nanoparticles for drug release experiments was conducted with the strepo-avidin-alkaline phosphatase conjugate in variable conditions of pH value, coating buffer, and reaction temperature. Protein-coated syndiotactic PVA micro- and nanoparticles, which does not crosslinking, were more superior to controllability of drug release, durability, and dimensional stability to water and blood than atactic one.

  1. Controlled release of retinyl acetate from ?-cyclodextrin functionalized poly(vinyl alcohol) electrospun nanofibers.

    PubMed

    Lemma, Solomon M; Scampicchio, Matteo; Mahon, Peter J; Sbarski, Igor; Wang, James; Kingshott, Peter

    2015-04-01

    Retinyl acetate (RA) was effectively incorporated into electrospun nanofibers of poly(vinyl alcohol) (PVA) containing ?-cyclodextrin (?-CD) in order to form inclusion complexes for encapsulation to prolong shelf life and thermal stability. The physical and thermal properties of encapsulated RA were determined by scanning electron microscopy (SEM), X-ray diffraction (XRD), and differential scanning calorimetry (DSC). The nanofibers of PVA/RA and PVA/RA/?-CD exhibited bead free average fiber diameters of 264 ± 61 and 223 ± 49 nm, respectively. The surface chemistry of the functional nanofibers was investigated by X-ray photoelectron spectroscopy (XPS). Thermogravimetric analysis (TGA) demonstrated different thermal stabilities between the bioactive and the polymer, with and without ?-CD. Square-wave voltammogram peak current changes were used to follow the release kinetics of RA from the nanofibers. Results indicate that RA coated inside PVA/?-CD nanofibers was protected against oxidation much better than RA in PVA nanofibers and should extend the shelf life. In addition, RA encapsulated in the PVA/?-CD had better thermal stability than PVA nanofibers. PMID:25779354

  2. Dissection and hemostasis with hydroxilated polyvinyl acetal tampons in open thyroid surgery

    PubMed Central

    Dionigi, Gianlorenzo; Boni, Luigi; Rovera, Francesca; Dionigi, Renzo

    2007-01-01

    Background The essential objectives for thyroidectomy are: avoidance of injury to the recurrent laryngeal nerves, conservation of the parathyroid glands, an accurate haemostasis and an excellent cosmesis. In the last 10 years major improvements and new technologies have been proposed and applied in thyroid surgery; among these mini-invasive thyroidectomy, regional anaesthesia and intraoperative neuromonitoring, and new devices for achieving dissection and haemostasis. Minor bleeding from small vessels could be a major complication in thyroid surgery. The purpose of ligating vessels is to maintain the surgical site free from an excess of blood and reduce blood loss in the patient. Materials and methods Hydroxylated polyvinyl acetal tampons (HPA) are made by a synthetic, open cell foam structure able to absorb fluids up to 25 times the initial weight. We tested their efficacy for small bleeding control and tissue dissection during several thyroid procedures. Results HPA tampons have been found extremely useful to absorb blood coming from minor and diffuse loss, helping to control bleeding by a combined action of fluid absorption and local compression. The porous design of the tampon allows the use of the suction device right through the tampon itself. Thanks to the initial mildly hard consistency, we also used HPA tampons as dissecting instruments. Conclusion In our experience the use of HPA tampons resulted extremely efficient for minor bleeding control, fluids removal and tissue dissection during thyroid surgery. PMID:17411448

  3. Studies on thermal analysis and optical parameters of Cu doped poly(vinyl acetate)/polyindole composites

    NASA Astrophysics Data System (ADS)

    Bhagat, D. J.; Dhokane, G. R.

    2015-05-01

    This article reports investigation on optical parameters and thermal analysis of Cu doped poly(vinyl acetate)/polyindole composites using cupric chloride as an oxidant. The study's complex optical parameters were determined through ultraviolet-visible (UV-vis) spectroscopy. Thermal analysis was done through thermo gravimetric analysis (TGA) and differential thermal analysis (DTA). The optical band gap values were found in the range 3.4381-4.8646 eV that reflects that synthesized composites have the potential to have application in optical devices and solar cells. The optical conductivity of composites is calculated to be 1.608 × 107 S-1.

  4. Microwave irradiation induced modifications on the interfaces in SAN/EVA/PVC and PVAc/BPA/PVP ternary polymer blends: Positron lifetime study

    NASA Astrophysics Data System (ADS)

    Dinesh, Meghala; Chikkakuntappa, Ranganathaiah

    2013-09-01

    Ternary polymer blends of poly(styrene-co-acrylonitrile)/poly(ethylene-co-vinylacetate)/poly(vinyl chloride) (SAN/EVA/PVC) and poly(vinyl acetate)/bisphenol A/polyvinylpyrrolidone (PVAc/BPA/PVP) with different compositions have been prepared by solvent casting method and characterized by positron lifetime spectroscopy and differential scanning calorimetry DSC. Phase modifications have been induced by irradiating the blends with microwave radiation. These changes have been monitored by measuring the free-volume content in the blends. The results clearly show improved interactions between the constituent polymers of the blends upon microwave irradiation. However, the free-volume data and DSC measurements are found to be inadequate to reveal the changes at the interfaces and the interfaces determine the final properties of the blend. For this we have used hydrodynamic interaction (?ij) approach developed by us to measure strength of hydrodynamic interaction at the interfaces. These results show that microwave irradiation stabilizes the interfaces if the blend contains strong polar groups. SAN/EVA/PVC blend shows an increased effective hydrodynamic interaction from -3.18 to -4.85 at composition 50/35/15 upon microwave irradiation and PVAc/BPA/PVP blend shows an increased effective hydrodynamic interaction from -3.81 to -7.57 at composition 20/50/30 after irradiation.

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

    NASA Astrophysics Data System (ADS)

    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).

  6. Selective formation of organo, organo-aqueous, and hydro gel-like materials from partially hydrolysed poly(vinyl acetate)s based on different boron-containing crosslinkers.

    PubMed

    Angelova, L V; Leskes, M; Berrie, B H; Weiss, R G

    2015-07-01

    Viscoelastic, gel-like, polymeric dispersions (HVPDs) can be prepared by crosslinking polyols with borax or boric acid in water under alkaline conditions. Rheologically similar HVPDs have been prepared in organic liquids containing no water or hydroxylic groups through crosslinking partially or fully hydrolysed poly(vinyl acetate)s with trimethyl borate, boric acid, or borax. The organo-HVPDs are water-sensitive and rheoreversible on exposure to water. They were characterised rheologically and by solution and solid-state (11)B NMR spectroscopy. Spectroscopic analyses show the presence of mono- and di-diol crosslinks, as well as non-crosslinked boron species in HVPDs prepared with trimethyl borate or boric acid. The number of crosslinks in organo-HVPDs prepared with borax increased over the course of several days. Results from solution and solid-state (11)B NMR spectroscopy are comparable; no solid-like component was detectable. We demonstrate that hydro, organo, or organo-aqueous HVPDs can be obtained from partially hydrolysed poly(vinyl acetate)s by 'tuning' the structure of the boron-based crosslinker. PMID:26027551

  7. Response to ``Comment on `Temperature divergence of the dynamics of a poly(vinyl acetate) glass: Dielectric vs. mechanical behaviors''' [J. Chem. Phys. 139, 137101 (2013)

    NASA Astrophysics Data System (ADS)

    Zhao, Jing; McKenna, Gregory B.

    2013-10-01

    R. Richert has made a comment to a paper of ours in which dielectric measures on poly(vinyl acetate) suggest that there is a change in temperature dependence of the temperature shift factors from Vogel-Fulcher-Tammann (VFT) to Arrhenius near to the glass transition temperature. He notes that we made an error in the description of his data and further notes that the data we did not use show a VFT behavior to well below the glass transition. Here we respond to the comment and add additional analysis that suggest that the differences in results are related to the differences between time temperature superposition (TTS) of data and fitting the data with a Kohlrausch, Williams, and Watts function. When TTS is used on the data from Wagner and Richert [Polymer 38, 255 (1997)] the change in behavior to Arrhenius-like below Tg is recovered.

  8. Comment on ``Temperature divergence of the dynamics of a poly(vinyl acetate) glass: Dielectric vs. mechanical behaviors'' [J. Chem. Phys. 136, 154901 (2012)

    NASA Astrophysics Data System (ADS)

    Richert, Ranko

    2013-10-01

    The temperature dependence of polymer dynamics below the standard glass transition is of considerable interest. Glassy relaxation dictates the process of physical aging, and understanding these slow dynamics helps in assessing a possible divergence at a finite temperature. In a recent paper, Zhao and McKenna have measured the equilibrium dynamics of poly(vinyl acetate) in the range from Tg - 15 K to Tg + 30 K using Struiks protocol [J. Zhao and G. B. McKenna, J. Chem. Phys. 136, 154901 (2012)]. In a figure that is meant to compare their results with dielectric relaxation data from Wagner and Richert [Polymer 38, 255 (1997)], dielectric retardation data from that work is shown instead. The corrected figure shows a considerable difference in the two measurements below Tg - 10 K, Arrhenius versus Vogel-Fulcher-Tammann behavior, and a possible source of the difference is discussed.

  9. A (polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer)-dispersed sustained-release tablet for imperialine to simultaneously prolong the drug release and improve the oral bioavailability.

    PubMed

    Lin, Qing; Fu, Yu; Li, Jia; Qu, Mengke; Deng, Li; Gong, Tao; Zhang, Zhirong

    2015-11-15

    Imperialine, extracted from Bulbus Fritillariae Cirrhosae, is an efficient antitussive and expectorant medicine. However, its short half-life and stomach degradation limited imperialine from further clinical use. The current study was conducted to develop a sustained-release tablet for imperialine both to prolong absorption time and to improve the oral bioavailability of the drug. The tablets were prepared by a direct compression method formulated on optimized solid dispersion (SD) for imperialine based on polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer (Soluplus(®)) with imperialine/Soluplus(®) ratio of 1:8 (w/w). In order to obtain the optimized formulation, factors that affected the drug release were investigated by in vitro dissolution studies in the media of pH1.2, 5.8, 7.0 and 7.4. Powder X-ray diffraction and scanning electron microscope confirmed that the imperialine in SD was amorphous instead of crystalline, and still stayed amorphous even after the direct compression. And besides, pharmacokinetic study in Beagle dogs was performed to inspect the in vivo sustained release. Plasma concentration-time curves and pharmacokinetic parameters were gained. As a result, the Cmax of imperialine was one-fold reduced and Tmax was two-fold prolonged, and the mean AUC0-24 was expressed as 89.581±21.243?gh/L, which showed that the oral bioavailability of imperialine was 2.46-fold improved. Moreover, the in vitro-in vivo correlation was recommended to carry out, demonstrating the percentages of drug release in vitro were well-correlated with the absorptive fraction in vivo with the correlation coefficients above 0.9900. By mathematically modeling and moment imaging of the drug release, Peppas equation was selected as the most fitted model for the sustained-release tablets with the diffusional coefficient in the range of 0.59-0.62, indicating the release of imperialine from the sustained-release tablets was an anomalous process involving polymer swelling, drug diffusion and matrix erosion. PMID:26349052

  10. Safety of PVAP and PVAP-T including a 90-day dietary toxicity study in rats and genotoxicity tests with polyvinyl acetate phthalate (PVAP).

    PubMed

    DeMerlis, C C; Schoneker, D R; Borzelleca, J F

    2014-08-01

    The safety of PVAP was evaluated in a 90-day subchronic toxicity study in rats. Sprague Dawley Crl:CD(SD) rats were administered a dietary concentration of 0.75%, 1.5% and 5.0% PVAP for a minimum of 90days. There were no adverse effects reported. The no-observed-adverse-effect level (NOAEL) in the 90-day sub chronic study was the 5% dietary concentration, which corresponds to a dose of 3120mg/kg/day for males and 3640mg/kg/day for females, the highest level tested. PVAP is co-processed with titanium dioxide to produce polyvinyl acetate phthalate and titanium dioxide (PVAP-T). The chemical composition, physiochemical properties and specifications of PVAP-T are unchanged during manufacturing process based on various analytical studies. Therefore, the toxicological data that support the safety of PVAP can be used to support the use of PVAP-T as a pharmaceutical excipient. An independent expert panel evaluated the safety of PVAP and PVAP-T. Based on the toxicology study results, safety assessment and the estimated exposure assessment for PVAP and PVAP-T, the expert panel concluded that PVAP and PVAP-T could safely be used in drug products up to 829mg per day which was the estimated exposure provided to the expert panel for current applications of PVAP and PVAP-T. PMID:24813760

  11. Molecular imprinting method for fabricating novel glucose sensor: Polyvinyl acetate electrode reinforced by MnO2/CuO loaded on graphene oxide nanoparticles.

    PubMed

    Farid, Mohammad Masoudi; Goudini, Leila; Piri, Farideh; Zamani, Abbasali; Saadati, Fariba

    2016-03-01

    An enzyme free glucose sensor was prepared by a molecular imprinting method (MIP). The procedure was developed by in situ preparation of a new polyvinyl acetate (PVA) electrode reinforced by MnO2/CuO loaded on graphene oxide (GO) nanoparticles (PVA/MnO2@GO/CuO). The nanocomposite was modified in the presence of glucose and then imprinted. A carbone paste method with voltammetry was used in the fabrication of the sensor from prepared MIP nanocomposite. PVA/MnO2@GO/CuO electrode was characterized by X-ray diffraction, FT-IR spectroscopy and scanning electron microscopy. Electrocatalytic activity of the electrode toward glucose oxidation was then investigated by cyclic voltammetry in alkaline medium. The results show that the response of PVA/MnO2@GO/CuO MIP is much higher than PVA/MnO2@GO/CuO non-imprinted electrode toward glucose oxidation. The detection limit was 53?M, and the sensor responses are linear for concentrations from 0.5 to 4.4mM. Relative standard deviations for intra- and inter-day determination were less than 6.0%. The relative recoveries for different samples were 96%. PMID:26471527

  12. A case-controlled, retrospective, comparative study on the use of biodegradable synthetic polyurethane foam versus polyvinyl acetate sponge after nasal fracture reduction.

    PubMed

    Jeong, H-S; Lee, H-K; Kim, H-S; Moon, M-S; Tark, K-C

    2014-06-01

    One of the most frequently used packing materials in closed reduction of a nasal bone fracture is the hydroxylated polyvinyl acetate sponge (PVAS; Merocel(®)); however this may cause synechia, epistaxis, and pain. Synthetic polyurethane foam (SPF; Nasopore(®) Forte) has recently been used in septoplasty to prevent synechia or restenosis and haematoma formation. The purpose of this study was to compare the effects of PVAS and SPF on postoperative appearance and discomfort following the reduction of nasal bone fractures. We retrospectively reviewed all patient questionnaires and medical histories, and clinical photographs and computed tomography scans obtained before and after surgery. Outcomes were assessed using the Global Aesthetic Improvement Scale (GAIS) score and visual analogue scale (VAS) scores, which were used to assess discomfort during the 6-month follow-up period. Postoperatively, there was no statistically significant difference in the GAIS for the two packing materials (P > 0.05). Postoperative epistaxis was observed at a significantly lower rate in the SPF group than in the PVAS group, whereas anterior rhinorrhea and posterior nasal drip occurred at significantly higher rates following removal of packing in the SPF group (P < 0.05). The results of this study suggest that synthetic dissolvable polyurethane may be a reliable alternative material for nasal packing and postoperative management following the reduction of nasal bone fractures. PMID:24613644

  13. Effect of monomer sequence distribution in poly(vinyl alcohol-co-vinyl acetate) on the hydrogen bonding structure and physical properties

    NASA Astrophysics Data System (ADS)

    Tasaka, Shun; Urakawa, Osamu; Inoue, Tadashi

    2015-03-01

    It has been well known that hydrogen (H-) bonding interaction in polymer materials strongly affects their properties. For example, glass transition temperature (Tg) and terminal relaxation time increase by introducing H-bonding sites. This is because the molecular motion is restricted due to the formation of inter- and intra-chain H-bonds. For H-bonding copolymers in which H-bonding monomer and non- bonding one are incorporated, the fraction dependence of their properties has been examined so far. However, the influence of sequence distribution on their properties has not been studied in detail. In this work, we investigated the H-bonding structure and physical properties of molten poly(vinyl alcohol-co-vinyl acetate) with different monomer sequences to clarify the effect of the sequence distribution. We found that, with increasing the randomness in monomer sequences, the number of H-bonds between carbonyl group and hydroxyl (OH) group increased. Moreover, OH groups form linearly connected structure (OH-OH-OH) and its number also increases with the sequence randomness. Tg for the samples with higher sequence randomness are higher than those with lower randomness for high VOH copolymers. These results indicate that formation of larger number of H-bonds makes Tg higher.

  14. Rapid and Quasi-reversible Poly(vinyl acetate-b-vinyl alcohol) Spherical Micelle Fusion Induced by Poly(ethylene oxide) in Water

    NASA Astrophysics Data System (ADS)

    Mahanthappa, Mahesh; Repollet-Pedrosa, Milton

    2014-03-01

    Methods for triggering morphology changes in aqueous dispersions of amphiphilic block copolymers (ABCs) are crucial for their development as responsive fluids with properties that may be manipulated ``on demand.'' Numerous groups have reported methods for switching the morphologies of ABCs by the incorporation of thermal and photochemical switches, the addition of salts, and changes in pH. We report a new ABC system in which a dispersion of spherical micelles may be rapidly and quasi-reversibly transformed into a solution of worm-like micelles, upon the addition of a water-soluble homopolymer. More specifically, we demonstrate that the addition of varying amounts of poly(ethylene oxide) homopolymer to a dilute dispersion of poly(vinyl acetate-block-vinyl alcohol) spherical micelles results in either (1) their immediate precipitation, or (2) their rapid fusion into worm-like micelles. Dilution of the latter solution of worm-like micelles with pure water induces their reversion into spherical micelles. By evaluating the effects of PEO molecular weight and solution concentration on the micellar interconversion process, we propose two possible mechanisms for this unexpected morphological transformation.

  15. Manipulating the morphologies of poly(vinyl alcohol) block copolymer surfactants

    NASA Astrophysics Data System (ADS)

    Repollet-Pedrosa, Milton H.

    Amphiphilic block copolymers (ABCs) are macromolecules containing well-defined hydrophilic and hydrophobic segments that self-assemble into nanoscale aggregates such as spherical and cylindrical micelles and vesicles, when dispersed in block-selective solvents. ABCs possess a miniscule critical micelle concentration, which results in kinetically trapped and persistent assemblies in solution with slow chain exchange between aggregates. This makes them useful as rheological modifiers for personal care products, enhanced oil recovery, and drug delivery formulations. Their utility in many of these applications is crucially dependent on the ability to control the micellar morphologies that they adopt in selective solvents. Triggering ABC micellar morphological transformations, i.e. from spherical to cylindrical micelles, is important for generating "on-demand" stimuli-responsive morphologies that control the aggregate morphology and the bulk solution properties in any given application. In this thesis, we develop the straightforward synthesis of biodegradable and biocompatible ABCs comprised of poly(vinyl acetate) (PVAc) and poly(vinyl alcohol) (PVA), with narrow molecular distributions and variable yet well-defined compositions. These block copolymer amphiphiles readily form spherical micelles in aqueous dispersions. We demonstrate that the addition of a water-soluble poly(ethylene oxide) (PEO) homopolymer to these dispersions results in a rapid transformation of these spherical micelles into cylindrical micelles. Dilution of these cylindrical micelles with water induces their reversion to spherical micelles. Our results indicate that the reversible morphology change depends sensitively on the PEO homopolymer concentration and molecular weight, as well as the length of the PVA corona block of the micelles. Through a series of quantitative 1H NMR studies, we found that the preferential partitioning of PEO homopolymer into the PVAc micellar core drives this morphological transformation. We also investigated the aqueous micellar self-assembly of non-covalent amphiphilic block copolymers (NC-ABCs) derived from complexation of an anionic gemini dicarboxylate surfactant (Na-96) to poly(ethylene oxide)-block -poly(2-(methacryloyloxy)-ethyltrimethylammonium chloride) (mPEO- b-qPDMAEMAxCl)(x = 48 or 110) at charge stoichiometries of [qDMAEMA+]:[COO -] = 1:1 and 1:0.5. Our results demonstrate that these polymer/surfactant complexes adopt rod-like conformations, the liquid crystallinity of which drives the formation of facetted vesicles and hollow tubular micelles.

  16. Multielectrode Pulmonary Vein Ablation Catheter (PVAC(®)): current data on results and risks.

    PubMed

    Mönnig, Gerold; Eckardt, Lars

    2014-12-01

    Electrical isolation of pulmonary veins is the cornerstone of catheter ablation for patients with symptomatic atrial fibrillation. However, uncertainty surrounds the choice of energy source in pulmonary vein isolation (PVI). Various alternative techniques such as the Pulmonary Vein Ablation Catheter (PVAC(®), Medtronic Inc., Minneapolis, MN, USA) have been developed to facilitate PVI. This over-the-wire multielectrode catheter is delivering duty-cycled bipolar and unipolar radiofrequency (RF) energy at relatively low power.PVI with this "one-shot" PVACatheter can shorten the procedure duration and lower fluoroscopy time compared to irrigated RF. It enables mapping and ablation with the same array, but fails to show signals during RF energy delivery. The effectiveness of PVAC is comparable to other technologies in randomized studies. The overall complication rate of PVAC PVI is comparable to irrigated RF and possibly slightly higher for cryoballoon PVI. Special attention has to be paid to an effective anticoagulation throughout the ablation procedure, avoidance of embolic events and pulmonary venous stenosis.The novel catheter design of the PVAC Gold(®) array may improve safety by reducing embolic events through avoidance of electrode 1-to-10 interaction and by better tissue contact due to the 20° forward tilt. Although clinical data with this new array are lacking so far, the PVAC system has been shown to be a promising tool for PVI. However, prospective studies especially with the novel array are required to determine its true role for catheter ablation of atrial fibrillation in the future. PMID:25070931

  17. (Au/PANA/PVAc) nanofibers as a novel composite matrix for albumin and streptavidin immobilization.

    PubMed

    Golshaei, Rana; Guler, Zeliha; Sarac, Sezai A

    2016-03-01

    A novel electrospun nanofiber mat (Au/PANA/PVAc) consists of (Gold/Poly Anthranilic acid) (Au/PANA) core/shell nanostructures as a support material for protein immobilization that was developed and characterized by electrochemical impedance spectroscopy. In the core/shells, PANA served carboxyl groups (-COOH) for covalent protein immobilization and Au enhanced the electrochemical properties by acting as tiny conduction centers to facilitate electron transfer. Covalent immobilization of albumin and streptavidin as model proteins onto the (Au/PANA/PVAc) nanofibers was carried out by using 1-ethyl-3-(dimethyl-aminopropyl) carbodiimide hydrochloride (EDC)/N-hydroxyl succinimide (NHS) activation. PVAc nanofibers were compared with Au/PANA/PVAc nanofibers before and after protein immobilization. The successful covalent binding of both albumin and streptavidin onto (Au/PANA/PVAc) nanofibers was confirmed by FTIR-ATR, Electron Microscopy/Energy-Dispersive X-ray Spectroscopy SEM/EDX and Electrochemical impedance spectroscopy (EIS). The nanofibers became resistive due to protein immobilization and the higher charge transfer resistance was observed after higher amount of protein was immobilized. PMID:26706530

  18. Modeling and optimization of electrospun polyvinylacetate (PVAc) nanofibers by response surface methodology (RSM).

    PubMed

    Park, Ju-Young; Shim, Wang-Geun; Lee, In-Hwa

    2011-02-01

    Response surface methodology (RSM), a collection of statistical and mathematical techniques, has been widely used to optimize and design operating conditions. Although this method is suitable for optimizing experimental conditions, very few attempts have been made on the electrospinning process. In this work, RSM was used to model and optimize of the electrospinning parameters for polyvinylacetate (PVAc) nanofibers. PVAc solution in acetone was electrospun under various conditions such as concentration of spinning solution and applied voltage. The experimental results indicate that concentrations of solution and applied voltage played an important role on the diameter size of PVAc nanofibers. The second order polynomial function was used to correlate the fiber diameter with the production variables. The predicted fiber diameters were in good agreement with the experimental results. PMID:21456188

  19. Complex AC impedance, transference number and vibrational spectroscopy studies of proton conducting PVAc-NH 4SCN polymer electrolytes

    NASA Astrophysics Data System (ADS)

    Selvasekarapandian, S.; Baskaran, R.; Hema, M.

    2005-03-01

    The polymer electrolytes composed of poly (vinyl acetate) (PVAc) with various stoichiometric ratios of ammonium thiocyanate (NH 4SCN) salt have been prepared by solution casting method. The polymer-salt complex formation and the polymer-proton interactions have been analysed by FT-IR spectroscopy. The conductivity and dielectric measurements are carried out on these films as a function of frequency at various temperatures. The complex impedance spectroscopy results reveal that the high-frequency semicircle is due to the bulk effect of the material. The conductivity is found to increase in the order of 10 -8-10 -4 S cm -1 at 303 K with the increase in salt concentration. The ionic transference number of mobile ions has been estimated by Wagner's polarization method and the results reveal that the conducting species are predominantly due to ions. The transient ionic current (TIC) measurement technique has been used to detect the type of mobile species and to evaluate their mobilities. The dielectric spectra show the low-frequency dispersion, which is due to the space charge effects arising from the electrodes.

  20. Preparation and properties of poly(vinyl alcohol)/chitosan blend bionanocomposites reinforced with cellulose nanocrystals/ZnO-Ag multifunctional nanosized filler

    PubMed Central

    Azizi, Susan; Ahmad, Mansor Bin; Hussein, Mohd Zobir; Ibrahim, Nor Azowa; Namvar, Farideh

    2014-01-01

    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. PMID:24790433

  1. Cellulose Nanocrystals/ZnO as a Bifunctional Reinforcing Nanocomposite for Poly(vinyl alcohol)/Chitosan Blend Films: Fabrication, Characterization and Properties

    PubMed Central

    Azizi, Susan; Ahmad, Mansor B.; Ibrahim, Nor Azowa; Hussein, Mohd Zobir; Namvar, Farideh

    2014-01-01

    In this study, cellulose nanocrystals/zinc oxide (CNCs/ZnO) nanocomposites were dispersed as bifunctional nano-sized fillers into poly(vinyl alcohol) (PVA) and chitosan (Cs) blend by a solvent casting method to prepare PVA/Cs/CNCs/ZnO bio-nanocomposites films. The morphology, thermal, mechanical and UV-vis absorption properties, as well antimicrobial effects of the bio-nanocomposite films were investigated. It demonstrated that CNCs/ZnO were compatible with PVA/Cs and dispersed homogeneously in the polymer blend matrix. CNCs/ZnO improved tensile strength and modulus of PVA/Cs significantly. Tensile strength and modulus of bio-nanocomposite films increased from 55.0 to 153.2 MPa and from 395 to 932 MPa, respectively with increasing nano-sized filler amount from 0 to 5.0 wt %. The thermal stability of PVA/Cs was also enhanced at 1.0 wt % CNCs/ZnO loading. UV light can be efficiently absorbed by incorporating ZnO nanoparticles into a PVA/Cs matrix, signifying that these bio-nanocomposite films show good UV-shielding effects. Moreover, the biocomposites films showed antibacterial activity toward the bacterial species Salmonella choleraesuis and Staphylococcus aureus. The improved physical properties obtained by incorporating CNCs/ZnO can be useful in variety uses. PMID:24945313

  2. Preparation and properties of poly(vinyl alcohol)/chitosan blend bionanocomposites reinforced with cellulose nanocrystals/ZnO-Ag multifunctional nanosized filler.

    PubMed

    Azizi, Susan; Ahmad, Mansor Bin; Hussein, Mohd Zobir; Ibrahim, Nor Azowa; Namvar, Farideh

    2014-01-01

    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. PMID:24790433

  3. Effect of water in amorphous polyvinyl formal: insights from molecular dynamics simulation.

    PubMed

    Yin, Qiang; Zhang, Lin; Jiang, Bo; Yin, Qinjian; Du, Kai

    2015-01-01

    In this study, molecular dynamics simulations were performed to study the influence of water on polyvinyl formal. The effects of adding different concentrations of water (0, 0.23, 0.47, 0.94, 1.40, 1.86, 2.76, 3.65 and 4.52 wt%) to a copolymer of polyvinyl acetal, polyvinyl alcohol, and polyvinyl acetate were investigated. Simulated results clearly indicated that the radius of gyration of the polymer chain decreased whereas the cohesive energy density increased with the addition of water molecules. The diffusion coefficient initially decreased and then monotonically increased with increasing water concentration, and the same trend was observed for the fractional free volume. The results provide insights into the molecular structural and physical properties of polyvinyl formal with different water contents. PMID:25605599

  4. Gold nanorods contained polyvinyl alcohol/chitosan nanofiber matrix for cell imaging and drug delivery.

    PubMed

    Yan, Eryun; Cao, Minglu; Wang, Yuwei; Hao, Xiaoyuan; Pei, Shichun; Gao, Jianwei; Wang, Yan; Zhang, Zhuanfang; Zhang, Deqing

    2016-01-01

    Gold nanorods (AuNRs) that contained polyvinyl alcohol/chitosan (PVA/CS) hybrid nanofibers with dual functions are successfully fabricated by a simple electrospinning method. The results of transmission electron microscopy (TEM), X-ray diffraction (XRD) and energy dispersive X-ray (EDX) spectroscopy indicate that AuNRs are indeed encapsulated into the PVA/CS hybrid nanofibers. FTIR spectra results demonstrate that the chemical structures of PVA and CS are not affected when the AuNRs are introduced into the fibers. In vitro cytotoxicity test reveals that the hybrid fibers involving AuNRs are completely biocompatible. The as-prepared fibers can be used as a carrier for anticancer agent doxorubicin (DOX), and the drug is delivered into the cell nucleus. The AuNRs and DOX incorporated fibers are effective for inhibiting the growth and proliferation of ovary cancer cells and they can also be used as the cell imaging agent due to the unique optical properties of AuNRs. The nanofiber matrix combining two functions of cell imaging and drug delivery may be of great application potential in biomedical-related areas. PMID:26478408

  5. SOURCE ASSESSMENT: POLYVINYL CHLORIDE

    EPA Science Inventory

    This report summarizes data on air emissions from the polyvinyl chloride (PVC) industry. PVC is manufactured by 20 companies at 35 plants. Each plant uses one or more of four possible polymerization processes: (1) suspension polymerization, (2) emulsion polymerization, (3) bulk p...

  6. Comparative evaluation of tensile bond strength of a polyvinyl acetate-based resilient liner following various denture base surface pre-treatment methods and immersion in artificial salivary medium: An in vitro study

    PubMed Central

    Philip, Jacob M.; Ganapathy, Dhanraj M.; Ariga, Padma

    2012-01-01

    Background and Aim: This study was formulated to evaluate and estimate the influence of various denture base resin surface pre-treatments (chemical and mechanical and combinations) upon tensile bond strength between a poly vinyl acetate-based denture liner and a denture base resin. Materials and Methods: A universal testing machine was used for determining the bond strength of the liner to surface pre-treated acrylic resin blocks. The data was analyzed by one-way analysis of variance and the t-test (? =.05). Results: This study infers that denture base surface pre-treatment can improve the adhesive tensile bond strength between the liner and denture base specimens. The results of this study infer that chemical, mechanical, and mechano-chemical pre-treatments will have different effects on the bond strength of the acrylic soft resilient liner to the denture base. Conclusion: Among the various methods of pre-treatment of denture base resins, it was inferred that the mechano-chemical pre-treatment method with air-borne particle abrasion followed by monomer application exhibited superior bond strength than other methods with the resilient liner. Hence, this method could be effectively used to improve bond strength between liner and denture base and thus could minimize delamination of liner from the denture base during function. PMID:23293485

  7. In situ self cross-linking of polyvinyl alcohol battery separators

    NASA Technical Reports Server (NTRS)

    Philipp, W. H.; Hsu, L. C.; Sheibley, D. W. (inventors)

    1979-01-01

    A battery separator was produced from a polyvinyl alcohol sheet structure which was subjected to an in situ, self crosslinking process by selective oxidation of the 1,2 diol units present in the polyvinyl alcohol sheet structure. The 1,2 diol units were cleaved to form aldehyde end groups which subsequently crosslink through acetalization of the 1,3 diol units of the polyvinyl alcohol. Selective oxidation was achieved using a solution of a suitable oxidizing agent such as periodic acid or lead tetraacetate.

  8. Mesoxalaldehyde acetals

    SciTech Connect

    Gordeeva, G.N.; Kalashnikov, S.M.; Popov, Yu.N.; Kruglov, E.A.; Imashev, U.B.

    1987-11-10

    The treatment of methylglyoxal acetals by alkyl nitrites in the presence of the corresponding aliphatic alcohols and hydrochloric acid leads to the formation of linear mesoxalaldehyde acetals, whose structure was established by NMR spectroscopy and mass spectrometry. The major pathways for the decomposition of these molecules upon electron impact were established.

  9. Preparative-scale isoelectric trapping separations in a multicompartmental electrolyzer: implementation and monitoring 

    E-print Network

    Sinajon, Joseph Brian Montejo

    2009-05-15

    ,N,N?,N?,N?-penta-methylethylene- diammonio)cyclomaltoheptaose PreMCE Pressure mediated capillary electrophoresis PVA Poly(vinyl alcohol) PVAC Poly(vinyl acetate) PVP Poly(vinylpyrrolidone) QDAA N,N-bis(carboxymethyl)dimethylammonium hydroxide inner salt QDBA N...

  10. Phenylmercuric acetate

    Integrated Risk Information System (IRIS)

    Phenylmercuric acetate ; CASRN 62 - 38 - 4 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinog

  11. Ethyl acetate

    Integrated Risk Information System (IRIS)

    Ethyl acetate ; CASRN 141 - 78 - 6 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Eff

  12. Ammonium acetate

    Integrated Risk Information System (IRIS)

    Ammonium acetate ; CASRN 631 - 61 - 8 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic

  13. Vinyl acetate

    Integrated Risk Information System (IRIS)

    Vinyl acetate ; CASRN 108 - 05 - 4 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Eff

  14. Thallium acetate

    Integrated Risk Information System (IRIS)

    Jump to main content . Integrated Risk Information System Recent Additions | Contact Us Search : All EPA IRIS • You are here : EPA Home • Research • Environmental Assessment • IRIS • IRIS Summaries Redirect Page As of September 30 , 2009 , the assessment summary for Thallium acetate is included in t

  15. 76 FR 13660 - Polyvinyl Alcohol From Taiwan

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-14

    ...INTERNATIONAL TRADE COMMISSION [Investigation No. 731-TA-1088 (Final)] Polyvinyl Alcohol From Taiwan Determination On the...Polyvinyl Alcohol from Taiwan: Investigation No. 731-TA-1088 (Final). By order of the Commission. Issued: March 9,...

  16. Estimation of polyvinyl alcohol cryogel mechanical properties with four ultrasound elastography methods and comparison with gold standard testings.

    PubMed

    Fromageau, Jérémie; Gennisson, Jean-Luc; Schmitt, Cédric; Maurice, Roch L; Mongrain, Rosaire; Cloutier, Guy

    2007-03-01

    Tissue-mimicking phantoms are very useful in the field of tissue characterization and essential in elastography for the purpose of validating motion estimators. This study is dedicated to the characterization of polyvinyl alcohol cryogel (PVA-C) for these types of applications. A strict fabrication procedure was defined to optimize the reproducibility of phantoms having a similar elasticity. Following mechanical stretching tests, the phantoms were used to compare the accuracy of four different elastography methods. The four methods were based on a one-dimensional (1-D) scaling factor estimation, on two different implementations of a 2-D Lagrangian speckle model estimator (quasistatic elastography methods), and on a 1-D shear wave transient elastography technique (dynamic method). Young's modulus was investigated as a function of the number of freeze-thaw cycles of PVA-C, and of the concentration of acoustic scatterers. Other mechanical and acoustic parameters-such as the speed of sound, shear wave velocity, mass density, and Poisson's ratio-also were assessed. The Poisson's ratio was estimated with good precision at 0.499 for all samples, and the Young's moduli varied in a range of 20 kPa for one freeze-thaw cycle to 600 kPa for 10 cycles. Nevertheless, above six freeze-thaw cycles, the results were less reliable because of sample geometry artifacts. However, for the samples that underwent less than seven freeze-thaw cycles, the Young's moduli estimated with the four elastography methods showed good matching with the mechanical tensile tests with a regression coefficient varying from 0.97 to 1.07, and correlations R2 varying from 0.93 to 0.99, depending on the method. PMID:17375819

  17. Polymerization of vinyl acetate in bulk and emulsion by gamma irradiation

    NASA Astrophysics Data System (ADS)

    Mesquita, Andrea C.; Mori, Manoel N.; Andrade e Silva, Leonardo G.

    2004-09-01

    The vinyl acetate polymerization to produce poly(vinyl acetate) was carried out in bulk and emulsion using a 60Co gamma irradiator Gammacell-220 type. The irradiation was carried out in a dose rate of 5.25 and 5.30 kGy/h, respectively. The polymers obtained were characterized by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimeter (DSC) and gel permeation chromatography (GPC). Tests of density, hardness and Vicat softening temperature were carried out.

  18. Polyvinyl alcohol hydrogels for iontohporesis

    NASA Astrophysics Data System (ADS)

    Bera, Prasanta; Alam, Asif Ali; Arora, Neha; Tibarewala, Dewaki Nandan; Basak, Piyali

    2013-06-01

    Transdermal therapeutic systems propound controlled release of active ingredients through the skin into the systemic circulation in a predictive manner. Drugs administered through these systems escape first-pass metabolism and maintain a steady state scenario similar to a continuous intravenous infusion for up to several days. The iontophoresis deal with the systemic delivery of the bioactive agents (drug) by applying an electric current. It is basically an injection without the needle. The iontophoretic system requires a gel-based matrix to accommodate the bioactive agent. Hydrogels have been used by many investigators in controlled-release drug delivery systems because of their good tissue compatibility and easy manipulation of swelling level and, thereby, solute permeability. In this work we have prepared polyvinyl alcohol (PVA) hydrogel. We have cross linked polyvinyl alcohol chemically with Glutaraldehyde with different wt%. FTIR study reveals the chemical changes during cross linking. Swelling in water, is done to have an idea about drug loading and drug release from the membrane. After drug loading to the hydrogels, we have studied the drug release property of the hydrogels using salicylic acid as a model drug.

  19. 21 CFR 177.1670 - Polyvinyl alcohol film.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyvinyl alcohol film. 177.1670 Section 177.1670... Contact Surfaces § 177.1670 Polyvinyl alcohol film. Polyvinyl alcohol film may be safely used in contact..., in accordance with the following prescribed conditions: (a) The polyvinyl alcohol film is...

  20. Three methods for in situ cross-linking of polyvinyl alcohol films for application as ion-conducting membranes in potassium hydroxide electrolyte. [battery separators

    NASA Technical Reports Server (NTRS)

    Philipp, W. H.; Hsu, L. C.

    1979-01-01

    Three methods of in situ cross-linking polyvinyl alcohol films are presented. They are: (1) acetalization with a dialdehyde such as glutaraldehyde, (2) acetalization with aldehyde groups formed by selective oxidative cleaving of the few percent of 1,2 diol units present in polyvinyl alcohol, and (3) cross-linking by hydrogen abstraction by reaction with hydrogen atoms and hydroxyl radicals from irradiated water. For the third method, improvement in film conductivity in KOH solution at the expense of mechanical strength is obtained by the presence of polyacrylic acid in the polyvinyl alcohol films. Resistivities in 45 percent KOH are given for in situ cross-linked films prepared by each of the three methods.

  1. 76 FR 13660 - Polyvinyl Alcohol From Taiwan

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-14

    ..., Washington, DC, and by publishing the notice in the Federal Register of October 4, 2010 (75 FR 61175). The... Publication 4218 (March 2011), entitled Polyvinyl Alcohol from Taiwan: Investigation No. 731-TA-1088...

  2. Preparation of vinyl acetate

    DOEpatents

    Tustin, G.C.; Zoeller, J.R.; Depew, L.S.

    1998-03-24

    This invention pertains to the preparation of vinyl acetate by contacting a mixture of hydrogen and ketene with a heterogeneous catalyst containing a transition metal to produce acetaldehyde, which is then reacted with ketene in the presence of an acid catalyst to produce vinyl acetate.

  3. 21 CFR 177.1670 - Polyvinyl alcohol film.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyvinyl alcohol film. 177.1670 Section 177.1670... Components of Single and Repeated Use Food Contact Surfaces § 177.1670 Polyvinyl alcohol film. Polyvinyl alcohol film may be safely used in contact with food of the types identified in § 176.170(c) of...

  4. 21 CFR 177.1670 - Polyvinyl alcohol film.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyvinyl alcohol film. 177.1670 Section 177.1670... Components of Single and Repeated Use Food Contact Surfaces § 177.1670 Polyvinyl alcohol film. Polyvinyl alcohol film may be safely used in contact with food of the types identified in § 176.170(c) of...

  5. 21 CFR 177.1670 - Polyvinyl alcohol film.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyvinyl alcohol film. 177.1670 Section 177.1670... Components of Single and Repeated Use Food Contact Surfaces § 177.1670 Polyvinyl alcohol film. Polyvinyl alcohol film may be safely used in contact with food of the types identified in § 176.170(c) of...

  6. 21 CFR 177.1670 - Polyvinyl alcohol film.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyvinyl alcohol film. 177.1670 Section 177.1670... Components of Single and Repeated Use Food Contact Surfaces § 177.1670 Polyvinyl alcohol film. Polyvinyl alcohol film may be safely used in contact with food of the types identified in § 176.170(c) of...

  7. The Acetate Switch

    PubMed Central

    Wolfe, Alan J.

    2005-01-01

    To succeed, many cells must alternate between life-styles that permit rapid growth in the presence of abundant nutrients and ones that enhance survival in the absence of those nutrients. One such change in life-style, the “acetate switch,” occurs as cells deplete their environment of acetate-producing carbon sources and begin to rely on their ability to scavenge for acetate. This review explains why, when, and how cells excrete or dissimilate acetate. The central components of the “switch” (phosphotransacetylase [PTA], acetate kinase [ACK], and AMP-forming acetyl coenzyme A synthetase [AMP-ACS]) and the behavior of cells that lack these components are introduced. Acetyl phosphate (acetyl?P), the high-energy intermediate of acetate dissimilation, is discussed, and conditions that influence its intracellular concentration are described. Evidence is provided that acetyl?P influences cellular processes from organelle biogenesis to cell cycle regulation and from biofilm development to pathogenesis. The merits of each mechanism proposed to explain the interaction of acetyl?P with two-component signal transduction pathways are addressed. A short list of enzymes that generate acetyl?P by PTA-ACKA-independent mechanisms is introduced and discussed briefly. Attention is then directed to the mechanisms used by cells to “flip the switch,” the induction and activation of the acetate-scavenging AMP-ACS. First, evidence is presented that nucleoid proteins orchestrate a progression of distinct nucleoprotein complexes to ensure proper transcription of its gene. Next, the way in which cells regulate AMP-ACS activity through reversible acetylation is described. Finally, the “acetate switch” as it exists in selected eubacteria, archaea, and eukaryotes, including humans, is described. PMID:15755952

  8. Polyvinyl alcohol as photoluminescent conductive polymer

    NASA Astrophysics Data System (ADS)

    Ruiz-Limón, B.; Wetzel, G. B. J.; Olivares-Pérez, A.; Ponce-Lee, E. L.; Hernández-Garay, M. P.; Páez-Trujillo, G.; Toxqui-López, S.; Fuentes-Tapia, I.

    2007-02-01

    We synthesized a photoluminescent conductor polymer composed of polyvinyl alcohol, which was doped with nickel chloride to decrease its resistivity (300 ?cm) and benzalkonium chloride to obtain photoluminescence properties, when it is radiated with a green laser beam (532 nm). We compared its absorbance curve and its energy emitted curve to observe the amount energy that is taken advantage of this process. Besides we research the photoluminescence behavior when an electric currant is applied in our conductor polymer, obtaining a modulation capacity.

  9. Hydrophilization of Polyvinyl Chloride Surface by Ozonation

    NASA Astrophysics Data System (ADS)

    Kurose, Keisuke; Okuda, Tetsuji; Nakai, Satoshi; Tsai, Tsung-Yueh; Nishijima, Wataru; Okada, Mitsumasa

    The surface modification mechanism of polyvinyl chloride (PVC) by ozonation was investigated to study the selective hydrophilization of PVC surface among other plastics. Infrared analysis confirmed the increase of hydrophilic groups. XPS analysis revealed that the increase was due to the structural change in chlorine group in PVC to hydroxylic acid, ketone, and carboxylic groups by ozonation. This chemical reaction by ozone could occur only for polymers with chlorides in its structure and resulted in the selective hydrophilization of PVC among various polymers.

  10. Preparation of novel carbon microfiber/carbon nanofiber-dispersed polyvinyl alcohol-based nanocomposite material for lithium-ion electrolyte battery separator.

    PubMed

    Sharma, Ajit K; Khare, Prateek; Singh, Jayant K; Verma, Nishith

    2013-04-01

    A novel nanocomposite polyvinyl alcohol precursor-based material dispersed with the web of carbon microfibers and carbon nanofibers is developed as lithium (Li)-ion electrolyte battery separator. The primary synthesis steps of the separator material consist of esterification of polyvinyl acetate to produce polyvinyl alcohol gel, ball-milling of the surfactant dispersed carbon micro-nanofibers, mixing of the milled micron size (~500 nm) fibers to the reactant mixture at the incipience of the polyvinyl alcohol gel formation, and the mixing of hydrophobic reagents along with polyethylene glycol as a plasticizer, to produce a thin film of ~25 ?m. The produced film, uniformly dispersed with carbon micro-nanofibers, has dramatically improved performance as a battery separator, with the ion conductivity of the electrolytes (LiPF6) saturated film measured as 0.119 S-cm(-1), approximately two orders of magnitude higher than that of polyvinyl alcohol. The other primary characteristics of the produced film, such as tensile strength, contact angle, and thermal stability, are also found to be superior to the materials made of other precursors, including polypropylene and polyethylene, discussed in the literature. The method of producing the films in this study is novel, simple, environmentally benign, and economically viable. PMID:23827627

  11. Effect of Heat Treatment on Some Mechanical Properties of Laminated Window Profiles Manufactured Using Two Types of Adhesives

    PubMed Central

    Korkut, Derya Sevim; Korkutand, Suleyman; Dilik, Tuncer

    2008-01-01

    The mechanical properties of laminated window profiles manufactured using two types of adhesives were determined. The objective of this study is to evaluate the effects of heat treatment on some mechanical properties of laminated window profiles that manufactured from Kosipo (Entandrophragma candollei Harms.) using differenet type adhesives. Commercially produced polyurethane based Macroplast UR 7221 and polyvinyl acetate (PVAc) adhesive were used for experiments. The overall test results were found to be comparable to those obtained in the previous studies. Both types of adhesives resulted in significant differences in their strength characteristics at 95% confidence level. Adhesive UR 7221 improved the overall properties of the samples in contrast to PVAc. PMID:19325761

  12. 78 FR 20890 - Polyvinyl Alcohol From Taiwan: Preliminary Results of Antidumping Duty Administrative Review...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-04-08

    ...Administration [A-583-841] Polyvinyl Alcohol From Taiwan: Preliminary Results...the antidumping duty order on polyvinyl alcohol (PVA) from Taiwan. The period...Duty Administrative Review: Polyvinyl Alcohol from Taiwan;...

  13. 78 FR 39256 - Polyvinyl Alcohol From Taiwan: Rescission of Antidumping Duty Administrative Review; 2012-2013

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-07-01

    ...Administration [A-583-841] Polyvinyl Alcohol From Taiwan: Rescission of...the antidumping duty order on polyvinyl alcohol (PVA) from Taiwan for the...CCPC to the Department, ``Polyvinyl Alcohol from Taiwan: Withdrawal...

  14. 75 FR 38079 - Postponement of Preliminary Determination of Antidumping Duty Investigation: Polyvinyl Alcohol...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-07-01

    ...Antidumping Duty Investigation: Polyvinyl Alcohol From Taiwan AGENCY: Import...antidumping duty investigation on polyvinyl alcohol from Taiwan. See Initiation...Anti-Dumping Duty Investigation: Polyvinyl Alcohol From Taiwan, 69 FR...

  15. 76 FR 42613 - National Emission Standards for Hazardous Air Pollutants for Polyvinyl Chloride and Copolymers...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-19

    ...Hazardous Air Pollutants for Polyvinyl Chloride and Copolymers Production; Extension...Hazardous Air Pollutants for Polyvinyl Chloride and Copolymers Production is being extended...the May 20, 2011, Proposed Polyvinyl Chloride and Copolymers Production Rule,...

  16. 76 FR 30604 - National Emission Standards for Hazardous Air Pollutants for Polyvinyl Chloride and Copolymers...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-05-26

    ...Hazardous Air Pollutants for Polyvinyl Chloride and Copolymers Production AGENCY: Environmental...Hazardous Air Pollutants for Polyvinyl Chloride and Copolymers Production. The EPA is...Hazardous Air Pollutants for Polyvinyl Chloride and Copolymers Production, under...

  17. Complex compound polyvinyl alcohol-titanic acid/titanium dioxide

    NASA Astrophysics Data System (ADS)

    Prosanov, I. Yu.

    2013-02-01

    A complex compound polyvinyl alcohol-titanic acid has been produced and investigated by means of IR and Raman spectroscopy, X-ray diffraction, and synchronous thermal analysis. It is claimed that it represents an interpolymeric complex of polyvinyl alcohol and hydrated titanium oxide.

  18. How To Learn and Have Fun with Poly(Vinyl Alcohol) and White Glue

    NASA Astrophysics Data System (ADS)

    de Zea Bermudez, V.; Passos de Almeida, P.; Féria Seita, J.

    1998-11-01

    The general behavior of Newtonian, shear-thinning, shear-thickening, thixotropic, negative thixotropic, and viscoelastic fluids is characterized and briefly discussed in terms of existing theoretical models. Whenever possible, examples of these types of fluids taken from everyday life are given for better understanding. This theoretical introduction is the basis for same, simple, and inexpensive laboratory work employing no special glassware and generally done by pairs of students. The work involves the synthesis of two well-known viscoelastic materials displaying unique properties: poly(vinyl alcohol) (PVA) and white glue, a poly(vinyl acetate)-based emulsion. The students are asked to perform a series of representative mechanical tests on both gels and to describe their observations in full detail. In particular, they are expected to recognize and identify the origin of the intriguing behaviors found (elasticity, spinability, self-siphoning effect, die-swell effect, Weissenberg effect). The tests include the preparation of fibers by extrusion, introducing concepts such as water solubility, hydrogen bonding, and glass transition temperature. The long list of questions, which ideally should be answered at the end of the laboratory work, allows the students to apply the new concepts acquired.

  19. Process for the extrusion of compositions comprising polypropylene, polyvinyl alcohol and a polypropylene-polyvinyl alcohol adhesive

    SciTech Connect

    Derrick, W.E.

    1989-04-18

    This patent describes a process for extruding a composition comprising polyvinyl alcohol, a polypropylene-polyvinyl alcohol adhesive and a plypropylene prepared with a high activity polymerization catalyst. The improvement consists of utilizing polypropylene having from about 50 to about 5000 ppm by weight of hydrotalcite incorporated therein to substantially eliminate gel formation.

  20. [Migration of di(2-ethylhexyl) phthalate from polyvinyl chloride tubes used in preparation of foods].

    PubMed

    Tsumura, Yukari; Ishimitsu, Susumu; Hirayama, Kuni; Fujimaki, Teruhisa; Nakazawa, Hiroyuki; Tonogai, Yasuhide

    2002-08-01

    Three samples of polyvinyl chloride products for food use were examined for di(2-ethylhexyl) phthalate (DEHP) migration levels under the conditions described in the Japanese Food Sanitation Law. These samples were two kinds of tubes and one stretched film, containing 12 to 41% DEHP by weight. DEHP migration levels from them were very low, all below 0.1 ppm, into 3 kinds of food simulant; water, 4% acetic acid and 20% ethanol. However, high levels of DEHP migrated into n-heptane, 12 ppm from the stretched film sample and more than 800 ppm from the tube samples. Migration from the 2 tubes was higher than 150 ppm, the limit of residues after evaporation in containers and wraps. Though the limit of residues after evaporation is not set for equipment used in the preparation of foods, the tested tubes were considered to be unsuitable for uses in which they come into direct contact with oils, fats or oily foods. PMID:12436721

  1. Preparation of porous super-hydrophobic and super-oleophilic polyvinyl chloride surface with corrosion resistance property

    NASA Astrophysics Data System (ADS)

    Kang, Yingke; Wang, Jinyan; Yang, Guangbin; Xiong, Xiujuan; Chen, Xinhua; Yu, Laigui; Zhang, Pingyu

    2011-11-01

    Porous super-hydrophobic polyvinyl chloride (PVC) surfaces were obtained via a facile solvent/non-solvent coating process without introducing compounds with low surface energy. The microstructure, wetting behavior, and corrosion resistance of resultant super-hydrophobic PVC coatings were investigated in relation to the effects of dosage of glacial acetic acid and the temperature of drying the mixed PVC solution spread over glass slide substrate. As-prepared PVC coatings had porous microstructure, and the one obtained at a glacial acetic acid to tetrahydrofuran volume ratio of 2.5:10.0 and under a drying temperature of 17 °C had a water contact angle of 150 ± 1.5°, showing super-hydrophobicity. In the meantime, it possessed very small contact angles for liquid paraffin and diiodomethane and good corrosion resistance against acid and alkali corrosive mediums, showing promising applications in self-cleaning, waterproof for outer wall of building, seawater resistant coating, and efficient separation of oil and water.

  2. 1 INTRODUCTION In Spain, Plasticized polyvinyl chloride (PVC-

    E-print Network

    Zornberg, Jorge G.

    1 INTRODUCTION In Spain, Plasticized polyvinyl chloride (PVC- P) geomembranes began being used chloride (PVC-P). This paper documents the initial characteristics of the geomembrane and its performance

  3. Polyvinyl alcohol cross-linked with two aldehydes

    NASA Technical Reports Server (NTRS)

    Sheibley, D. W.; Rieker, L. L.; Hsu, L. C.; Manzo, M. A. (inventors)

    1982-01-01

    A film forming polyvinyl alcohol resin is admixed, in aqueous solution, with a dialdehyde crosslinking agent which is capable of crosslinking the polyvinyl alcohol resin and a water soluble acid aldehyde containing a reactive aldehyde group capable of reacting with hydroxyl groups in the polyvinyl alcohol resin and an ionizable acid hydrogen atom. The dialdehyde is present in an amount sufficient to react with from 1 to 20% by weight of the theoretical amount required to react with all of the hydroxyl groups of the polyvinyl alcohol. The amount of acid aldehyde is from 1 to 50% by weight, same basis, and is sufficient to reduce the pH of the aqueous admixture to 5 or less. The admixture is then formed into a desired physical shape, such as by casting a sheet or film, and the shaped material is then heated to simultaneously dry and crosslink the article.

  4. 75 FR 15726 - Polyvinyl Alcohol From Taiwan; Determination

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-30

    ...COMMISSION [Investigation No. 731-TA-1088 (Preliminary) (Remand)] Polyvinyl...antidumping duty investigation No. 731- TA-1088 (Preliminary). Notice of the institution...Taiwan: Investigation No. 731- TA-1088 (Preliminary). Domestic...

  5. In Situ Cross-Linking of Polyvinyl Alcohol Films

    NASA Technical Reports Server (NTRS)

    Philipp, W. H.; Shu, L. C.; May, C. E.

    1984-01-01

    Films or impregnated matrices readily made from aqueous polyvinyl alcohol solution. Controlled thickness films made by casting precise quantities of aqueous polymer solution on smooth surface, allowing water to evaporate and then removing film. Composite separators formed in similar fashion by impregnating cloth matrix with polyvinyl alcohol solution and drying composite. Insoluble thin hydrophilic membranes made from aqueous systems, and use of undesirable organic solvents not required.

  6. Composite Films of Poly(vinyl alcohol) and Bifunctional Cross-linking Cellulose Nanocrystals.

    PubMed

    Sirviö, Juho Antti; Honkaniemi, Samuli; Visanko, Miikka; Liimatainen, Henrikki

    2015-09-01

    Long and flexible cellulose nanofibrils or stiff and short cellulose nanocrystals (CNCs) are both promising lightweight materials with high strength and the potential to serve as reinforcing agents in many polymeric materials. In this study, bifunctional reactive cellulose nanocrystals (RCNCs) with carboxyl and aldehyde functionalities were used as reinforcements to prepare acetal-bonding cross-linked poly(vinyl alcohol) (PVA) films. Two RCNCs were obtained through the mechanical homogenization of partially carboxylated dialdehyde cellulose (DAC) with a residual aldehyde content of 0.55 and 1.93 mmol/g and a carboxyl content of 1.65 and 1.93 mmol/g, respectively. The mechanical, thermal, and barrier properties of PVA-RCNC films with a variable mass ratio of RCNCs (0.5-10%) were determined. Reference CNCs without reactive aldehydes were obtained through the reduction of aldehyde functionalities to primary hydroxide groups, and their reinforcing effect was compared to RCNCs. With the addition of 10% acetal-bonding RCNCs with respect to PVA weight, the tensile strength and Young's modulus were up to 2-fold greater than those of pure PVA film. An addition of only 0.5% RCNCs improved the tensile strength of the PVA film by 66% and the modulus by 61%. In comparison, a significantly lower reinforcing effect (19% with CNC loading of 0.5%) was found using reference CNCs. PVA's effective oxygen barrier and thermal properties were preserved when RCNCs were introduced into the films. PMID:26280660

  7. Thermal, electrical and optical studies on the poly(vinyl alcohol) based polymer electrolytes

    NASA Astrophysics Data System (ADS)

    Hirankumar, G.; Selvasekarapandian, S.; Kuwata, N.; Kawamura, J.; Hattori, T.

    Solid polymer proton conductors comprising of poly(vinyl alcohol), ammonium acetate and water have been prepared by solution cast method for different NH 4+/OH - ratios. The XRD spectra for the electrolyte indicate that the amorphous nature of PVA increases with the concentration of ammonium acetate. The DSC curves show the low glass transition temperature for the ratio (NH 4+/OH -) = 0.25 which relates to higher conductivity of the sample. The ionic conductivity at room temperature depends strongly on NH 4+/OH - ratios. The variation of electrical conductivity with temperature showed two regions of activation above and below glass transition temperature. The optical absorption studies show the similar trend for pure PVA and salt-doped PVA with different absorption intensity. The direct and indirect band gap energy is observed to be constant for pure PVA and salt-doped PVA samples and found to be 5.4 eV and 4.8 eV, respectively. The dc polarization measurement shows that the conductivity is mainly due to ions.

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

    NASA Astrophysics Data System (ADS)

    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.

  9. 21 CFR 522.2476 - Trenbolone acetate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...milligrams (mg) trenbolone acetate (one implant consisting of 7 pellets, each pellet containing 20 mg trenbolone acetate) per implant dose. (B) 140 mg trenbolone acetate (one implant consisting of 8 pellets, each of 7...

  10. 21 CFR 184.1721 - Sodium acetate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...animal tissues. Sodium acetate may occur in either the anhydrous or trihydrated form. It is produced synthetically by the neutralization of acetic acid with sodium carbonate or by treating calcium acetate with sodium sulfate and sodium...

  11. 21 CFR 184.1721 - Sodium acetate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...animal tissues. Sodium acetate may occur in either the anhydrous or trihydrated form. It is produced synthetically by the neutralization of acetic acid with sodium carbonate or by treating calcium acetate with sodium sulfate and sodium...

  12. 21 CFR 184.1721 - Sodium acetate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...animal tissues. Sodium acetate may occur in either the anhydrous or trihydrated form. It is produced synthetically by the neutralization of acetic acid with sodium carbonate or by treating calcium acetate with sodium sulfate and sodium...

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

    NASA Astrophysics Data System (ADS)

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

    2013-07-01

    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 Cdbnd 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.

  14. Biochemistry of microbial polyvinyl alcohol degradation.

    PubMed

    Kawai, Fusako; Hu, Xiaoping

    2009-08-01

    Effect of minor chemical structures such as 1,2-diol content, ethylene content, tacticity, a degree of polymerization, and a degree of saponification of the main chain on biodegradability of polyvinyl alcohol (PVA) is summarized. Most PVA-degraders are Gram-negative bacteria belonging to the Pseudomonads and Sphingomonads, but Gram-positive bacteria also have PVA-degrading abilities. Several examples show symbiotic degradation of PVA by different mechanisms. Penicillium sp. is the only reported eukaryotic degrader. A vinyl alcohol oligomer-utilizing fungus, Geotrichum fermentans WF9101, has also been reported. Lignolytic fungi have displayed non-specific degradation of PVA. Extensive published studies have established a two-step process for the biodegradation of PVA. Some bacteria excrete extracellular PVA oxidase to yield oxidized PVA, which is partly under spontaneous depolymerization and is further metabolized by the second step enzyme (hydrolase). On the other hand, PVA (whole and depolymerized to some extent) must be taken up into the periplasmic space of some Gram-negative bacteria, where PVA is oxidized by PVA dehydrogenase, coupled to a respiratory chain. The complete pva operon was identified in Sphingopyxis sp. 113P3. Anaerobic biodegradability of PVA has also been suggested. PMID:19590867

  15. Hydrothermal carbonization of poly(vinyl chloride).

    PubMed

    Poerschmann, J; Weiner, B; Woszidlo, S; Koehler, R; Kopinke, F-D

    2015-01-01

    Poly(vinyl chloride) (PVC) was subjected to hydrothermal carbonization in subcritical water at 180-260 °C. Dehydrochlorination increased with increasing reaction temperature. The release of chlorine was almost quantitative above ?235 °C. The fraction of organic carbon (OC) recovered in the hydrochar decreased with increasing operating temperature from 93% at 180 °C to 75% at 250 °C. A wide array of polycyclic aromatic hydrocarbons (PAHs) could be detected in the aqueous phase, but their combined concentration amounted to only ?140 ?g g(-1) PVC-substrate at 240 °C. A pathway for the formation of cyclic hydrocarbons and O-functionalized organics was proposed. Chlorinated hydrocarbons including chlorophenols could only be identified at trace levels (low ppb). Polychlorinated dibenzodioxins (PCDDs) and dibenzofurans (PCDFs) could not be detected. The sorption potential of the hydrochar turned out to be very low, in particular for polar organic pollutants. Our results provide strong evidence that hydrothermal carbonization of household organic wastes which can be tied to co-discarded PVC-plastic residues is environmentally sound regarding the formation of toxic organic products. Following these findings, hydrothermal treatment of PVC-waste beyond operating temperatures of ?235 °C to allow complete release of organic chlorine should be further pursued. PMID:25150971

  16. Preparation and properties of polyvinyl alcohol microspheres

    SciTech Connect

    Campbell, J.H.; Grens, J.Z.; Poco, J.F.; Ives, B.H.

    1986-06-01

    Polyvinyl alcohol (PVA) microspheres, having a size range of approx.150- to 250-..mu..m diameter with 1- to 5-..mu..m wall thickness, have been fabricated using a solution droplet technique. The spheres were developed for possible use on the Lawrence Livermore National Laboratory (LLNL) Inertial Confinement Fusion (ICF) Program. PVA, a polymer chosen based on earlier survey work carried out at KMS Fusion, Inc., has good strength, low hydrogen permeability, is optically transparent, and water soluble. The latter property makes it safe and easy to use in our droplet generator system. A unique dual-orifice droplet generator was used to prepare the spheres. The droplet generator operating conditions and the column processing parameters were chosen using results from our 1-D model calculations as a guide. The polymer microsphere model is an extension of the model we developed to support the glass sphere production. After preparation, the spheres were physically characterized for surface quality, sphericity, wall thickness (and uniformity), and size. We also determined the buckling pressure for both uncoated and CH-coated spheres. Radiation stability to beta decay (from tritium) was evaluated by exposing the spheres to a 7-keV electron beam. The results from these and other physical property measurements are presented in this report.

  17. Piezoresistive Properties of Polyvinyl Chloride Composites

    NASA Astrophysics Data System (ADS)

    Toprakci, Hatice Aylin Karahan

    Textile based sensors provide an interface between the user and the electronic system by converting any type of physiological or environmental signal into electrical signals. Common applications include health monitoring, rehabilitation, multimedia, and surveillance. In this research we demonstrate fabrication of piezoresistive sensors on textile fabrics through application of a screen-printed conductive nanocomposite layer of plasticized poly(vinyl chloride) (PVC), and carbon nanofiber (CNF). In order to understand the behavior of conductive plastisol, morphological, mechanical and electrical properties of composite films were investigated for different molecular weights of PVC. Homogeneous filler dispersion and good filler/polymer interphase were observed without any dominant filler orientation. Mechanical and electrical properties were found to be affected by CNF, plasticizer content and matrix molecular weight. CNFs were found to provide substantial bridging in the matrix and enhance strength. These nanostructured composite sensors were found to be sensitive under different levels of strain which can be monitored by change in electrical resistance. Finally, we demonstrate the fabrication of piezoresistive sensors on textile fabrics through application of a screen-printed conductive nanocomposite layer of conductive plastisol. Conductive plastisol was found to show good adhesion to fabric with homogeneous CNF distribution. As in composite films, samples were found to show negative piezoresistance at different levels of strain. Strain level and filler concentration were found to affect the piezoresistive behavior and sensitivity of the printed sensors.

  18. Cytotoxicity associated with electrospun polyvinyl alcohol.

    PubMed

    Pathan, Saif G; Fitzgerald, Lisa M; Ali, Syed M; Damrauer, Scott M; Bide, Martin J; Nelson, David W; Ferran, Christiane; Phaneuf, Tina M; Phaneuf, Matthew D

    2015-11-01

    Polyvinyl alcohol (PVA) is a synthetic, water-soluble polymer, with applications in industries ranging from textiles to biomedical devices. Research on electrospinning of PVA has been targeted toward optimizing or finding novel applications in the biomedical field. However, the effects of electrospinning on PVA biocompatibility have not been thoroughly evaluated. In this study, the cytotoxicity of electrospun PVA (nPVA) which was not crosslinked after electrospinning was assessed. PVA polymers of several molecular weights were dissolved in distilled water and electrospun using the same parameters. Electrospun PVA materials with varying molecular weights were then dissolved in tissue culture medium and directly compared against solutions of nonelectrospun PVA polymer in human coronary artery smooth muscle cells and human coronary artery endothelial cells cultures. All nPVA solutions were cytotoxic at a threshold molar concentration that correlated with the molecular weight of the starting PVA polymer. In contrast, none of the nonelectrospun PVA solutions caused any cytotoxicity, regardless of their concentration in the cell culture. Evaluation of the nPVA material by differential scanning calorimetry confirmed that polymer degradation had occurred after electrospinning. To elucidate the identity of the nPVA component that caused cytotoxicity, nPVA materials were dissolved, fractionated using size exclusion columns, and the different fractions were added to HCASMC and human coronary artery endothelial cells cultures. These studies indicated that the cytotoxic component of the different nPVA solutions were present in the low-molecular-weight fraction. Additionally, the amount of PVA present in the 3-10 kg/mol fraction was approximately sixfold greater than that in the nonelectrospun samples. In conclusion, electrospinning of PVA resulted in small-molecular-weight fractions that were cytotoxic to cells. This result demonstrates that biocompatibility of electrospun biodegradable polymers should not be assumed on the basis of success of their nonelectrospun predecessors. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 103B: 1652-1662, 2015. PMID:25573200

  19. Electrochemical study of ferrocene intercalated vanadium pentoxide xerogel/polyvinyl alcohol composite films: Application

    E-print Network

    Trikalitis, Pantelis N.

    Electrochemical study of ferrocene intercalated vanadium pentoxide xerogel/polyvinyl alcohol film based on ferrocene intercalated vanadium pentoxide xerogel/polyvinyl alcohol (FeCp2/VXG reserved. Keywords: Vanadium pentoxide xerogel; Ferrocene; Intercalation; Amperometric glucose amperometric

  20. 77 FR 14342 - Polyvinyl Alcohol From Taiwan: Correction to Notice of Opportunity To Request Administrative Review

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-09

    ...International Trade Administration [A-583-841] Polyvinyl Alcohol From Taiwan: Correction to Notice of Opportunity...administrative review of the antidumping duty order on polyvinyl alcohol from Taiwan. See Antidumping or Countervailing...

  1. 40 CFR 61.64 - Emission standard for polyvinyl chloride plants.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...false Emission standard for polyvinyl chloride plants. 61.64 Section 61.64 ...National Emission Standard for Vinyl Chloride § 61.64 Emission standard for polyvinyl chloride plants. An owner or operator of a...

  2. 40 CFR 61.64 - Emission standard for polyvinyl chloride plants.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...false Emission standard for polyvinyl chloride plants. 61.64 Section 61.64 ...National Emission Standard for Vinyl Chloride § 61.64 Emission standard for polyvinyl chloride plants. An owner or operator of a...

  3. 40 CFR 61.64 - Emission standard for polyvinyl chloride plants.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...false Emission standard for polyvinyl chloride plants. 61.64 Section 61.64 ...National Emission Standard for Vinyl Chloride § 61.64 Emission standard for polyvinyl chloride plants. An owner or operator of a...

  4. 40 CFR 61.64 - Emission standard for polyvinyl chloride plants.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...false Emission standard for polyvinyl chloride plants. 61.64 Section 61.64 ...National Emission Standard for Vinyl Chloride § 61.64 Emission standard for polyvinyl chloride plants. An owner or operator of a...

  5. 40 CFR 61.64 - Emission standard for polyvinyl chloride plants.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...false Emission standard for polyvinyl chloride plants. 61.64 Section 61.64 ...National Emission Standard for Vinyl Chloride § 61.64 Emission standard for polyvinyl chloride plants. An owner or operator of a...

  6. 76 FR 30604 - National Emission Standards for Hazardous Air Pollutants for Polyvinyl Chloride and Copolymers...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-05-26

    ... Polyvinyl Chloride and Copolymers Production AGENCY: Environmental Protection Agency (EPA). ACTION: Proposed..., the proposed rule, National Emission Standards for Hazardous Air Pollutants for Polyvinyl Chloride and... Polyvinyl Chloride and Copolymers Production, under Docket ID No. EPA-HQ-OAR-2002-0037 (available at...

  7. ORIGINAL PAPER Natural Fiber Reinforced Poly(vinyl chloride) Composites: Effect

    E-print Network

    ORIGINAL PAPER Natural Fiber Reinforced Poly(vinyl chloride) Composites: Effect of Fiber Type Science+Business Media, LLC 2008 Abstract Poly(vinyl chloride) (PVC) and natural fiber composites were(vinyl chloride) (PVC) Á Composites Á Fibers Á SEBS Á Impact modifier Introduction Poly(vinyl chloride) (PVC

  8. Poly(vinyl alcohol) (PVA)/sulfonated polyhedral oligosilsesquioxane (sPOSS) hybrid membranes

    E-print Network

    Mather, Patrick T.

    Poly(vinyl alcohol) (PVA)/sulfonated polyhedral oligosilsesquioxane (sPOSS) hybrid membranes/inorganic hybrid membranes based on poly(vinyl alcohol) (PVA) and sulfonated polyhedral oligosilsesquioxane (s membrane. Copyright # 2007 John Wiley & Sons, Ltd. KEYWORDS: poly(vinyl alcohol) (PVA); sulfonated

  9. Polyvinyl alcohol battery separator containing inert filler. [alkaline batteries

    NASA Technical Reports Server (NTRS)

    Sheibley, D. W.; Hsu, L. C.; Manzo, M. A. (inventors)

    1981-01-01

    A cross-linked polyvinyl alcohol battery separator is disclosed. A particulate filler, inert to alkaline electrolyte of an alkaline battery, is incorporated in the separator in an amount of 1-20% by weight, based on the weight of the polyvinyl alcohol, and is dispersed throughout the product. Incorporation of the filler enhances performance and increases cycle life of alkaline batteries when compared with batteries containing a similar separator not containing filler. Suitable fillers include titanates, silicates, zirconates, aluminates, wood floor, lignin, and titania. Particle size is not greater than about 50 microns.

  10. EXPOSURE TO CHEMICAL ADDITIVES FROM POLYVINYL CHLORIDE POLYMER EXTRUSION PROCESSING

    EPA Science Inventory

    This report presents a model to predict worker inhalation exposure due to off-gassing of additives during polyvinyl chloride (PVC) extrusion processing. ata on off-gassing of additives were reviewed in the literature, the off-gassing at normal PVC processing temperatures was stud...

  11. 21 CFR 175.270 - Poly(vinyl fluoride) resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... polymerization of vinyl fluoride. (b) The poly(vinyl fluoride) basic resins have an intrinsic viscosity of not... Dilute Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference. Copies may be... Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference; see paragraph (b)...

  12. 21 CFR 175.270 - Poly(vinyl fluoride) resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... polymerization of vinyl fluoride. (b) The poly(vinyl fluoride) basic resins have an intrinsic viscosity of not... Dilute Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference. Copies may be... Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference; see paragraph (b)...

  13. 21 CFR 175.270 - Poly(vinyl fluoride) resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... polymerization of vinyl fluoride. (b) The poly(vinyl fluoride) basic resins have an intrinsic viscosity of not... Dilute Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference. Copies may be... Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference; see paragraph (b)...

  14. 21 CFR 175.270 - Poly(vinyl fluoride) resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... polymerization of vinyl fluoride. (b) The poly(vinyl fluoride) basic resins have an intrinsic viscosity of not... Dilute Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference. Copies may be... Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference; see paragraph (b)...

  15. Reductive opening of carbohydrate phenylsulfonylethylidene (PSE) acetals.

    PubMed

    Chéry, Florence; Cabianca, Elena; Tatibouët, Arnaud; De Lucchi, Ottorino; Lindhorst, Thisbe K; Rollin, Patrick

    2015-11-19

    The phenylsulfonylethylidene (PSE) acetal is a relatively new protecting group in carbohydrate chemistry. However, carbohydrate-derived phenylsulfonylethylidene (PSE) acetals show a different behavior in reductive desulfonylation than simple symmetrical acetals. Here we have investigated various SET-type reaction conditions in order to open PSE acetals regioselectively and to produce chiral ?-hydroxyethenyl ethers. Whereas sodium amalgam leads to a mixture of regioisomeric vinyl ethers besides the ethylidene acetal, samarium iodide is suited for regioselective ring opening. This is shown with seven different carbohydrate PSE acetals, both of the 1,3-dioxane and the 1,3-dioxolane type. PMID:26469209

  16. Polyvinyl alcohol {gamma}-ray grafted nylon 4 membrane for pervaporation and evapomeation

    SciTech Connect

    Lai, J.Y.; Chen, R.Y.; Lee, K.R

    1993-05-01

    Nylon 4, which possesses high mechanical strength and good affinity for water, can be considered as a liquid separation membrane. To improve the hydrophilicity of a Nylon 4 membrane for pervaporation and evapomeation processes, and to overcome the hydrolysis of polyvinyl alcohol (PVA), this study attempts to prepare a PVA-g-Nylon 4 membrane by {gamma}-ray irradiation grafting of vinyl acetate (VAc) onto Nylon 4 membrane, followed by hydrolysis treatment. The effects of down-stream pressure, irradiation dose, VAc monomer concentration, degree of grafting, feed composition, and size of alcohols on the separation of water-alcohol mixtures were studied. The surface properties of the prepared membrane were characterized by FTIR, ESCA, and a contact angle meter. A separation factor of 13.8 and a permeation rate of 0.352 kg/m{sup 2}-h can be obtained for a PVA-g-Nylon 4 membrane with a degree of grafting of 21.2% for a 90-wt% ethanol feed concentration. Compared to the pervaporation process, the evapomeation process has a significantly increased separation factor with a decreased permeation rate for the same PVA-g-Nylon 4 membrane. 24 refs., 9 figs., 4 tabs.

  17. Treatment of desizing wastewater containing poly(vinyl alcohol) by wet air oxidation

    SciTech Connect

    Chen, G.; Lei, L.; Yue, P.L.; Cen, P.

    2000-05-01

    The effectiveness of wet air oxidation (WAO) is studied in a 2-L autoclave for the treatment of desizing wastewater from man-made fiber textile plants. At an oxygen pressure of less than 2 MPa, over 30-min, chemical oxygen demand (COD) removal was found to increase from 15 to 65% when the temperature was raised from 150 to 250 C. The biodegradability of the wastewater was also simultaneously increased. Up to 90% of the COD could be removed within 120 min. A simplified reaction mechanism is proposed which involves a direct mineralization step in parallel with a step in which an intermediate is formed prior to mineralization. A kinetic model for COD removal was developed based on this reaction mechanism. The model was tested with experimental COD results over the temperature range of the experiments. The dependence of the specific reaction rate constants was found to follow the Arrhenius type of equation. The direct oxidation of poly(vinyl alcohol) (PVA) to carbon dioxide and water is the dominant reaction step. The intermediates formed are not likely to be the acetic acid but may be short segments of PVA that are easily oxidized.

  18. Solution spinning of a high-? oxide superconductor: the effect of poly(vinyl alcohol) spinning medium on the critical current density of melt-processed ? superconducting filaments

    NASA Astrophysics Data System (ADS)

    Tomita, Hisayo; Sunohara, Makoto; Goto, Tomoko; Takahashi, Kiyohisa

    1996-12-01

    The precursor 0953-2048/9/12/014/img9 filament was prepared by solution spinning through a homogeneous aqueous poly(vinyl alcohol) (PVA) solution of Y, Ba and Cu acetates. The solution spinning was successfully performed using PVA with degrees of polymerization (DP) of 1700 and 2450 and a degree of saponification of 85 mol%. The as-drawn filament was heated to remove volatile components and partially melted to generate a superconducting phase. The effects of the DP of PVA and a content of mixed acetates in the precursor filament on the critical current density 0953-2048/9/12/014/img10 of the melt-processed filament were examined. The higher 0953-2048/9/12/014/img11 was obtained for the filament spun from PVA solution of higher DP and lower acetate content. The highest 0953-2048/9/12/014/img11 value of 0953-2048/9/12/014/img13 at 77 K and 0 T was achieved for the filament spun from the DP 2450 PVA with an acetate to PVA ratio of two.

  19. 21 CFR 522.2476 - Trenbolone acetate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...DRUGS, FEEDS, AND RELATED PRODUCTS IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL...milligrams (mg) trenbolone acetate (one implant consisting of 7 pellets, each pellet containing 20 mg trenbolone acetate) per implant dose. (B) 140 mg trenbolone...

  20. Ozone decomposition in aqueous acetate solutions

    SciTech Connect

    Sehested, K.; Holcman, J.; Bjergbakke, E.; Hart, E.J.

    1987-01-01

    The acetate radical ion reacts with ozone with a rate constant of k = (1.5 +/- 0.5) x 10Z dmT mol s . The products from this reaction are CO2, HCHO, and O2 . By subsequent reaction of the peroxy radical with ozone the acetate radical ion is regenerated through the OH radical. A chain decomposition of ozone takes place. It terminates when the acetate radical ion reacts with oxygen forming the unreactive peroxy acetate radical. The chain is rather short as oxygen is developed, as a result of the ozone consumption. The inhibiting effect of acetate on the ozone decay is rationalized by OH scavenging by acetate and successive reaction of the acetate radical ion with oxygen. Some products from the bimolecular disappearance of the peroxy acetate radicals, however, react further with ozone, reducing the effectiveness of the stabilization.

  1. 21 CFR 582.1721 - Sodium acetate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Sodium acetate. 582.1721 Section 582.1721 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS....1721 Sodium acetate. (a) Product. Sodium acetate. (b) Conditions of use. This substance is...

  2. 21 CFR 582.1721 - Sodium acetate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Sodium acetate. 582.1721 Section 582.1721 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS....1721 Sodium acetate. (a) Product. Sodium acetate. (b) Conditions of use. This substance is...

  3. 21 CFR 582.1721 - Sodium acetate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Sodium acetate. 582.1721 Section 582.1721 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS....1721 Sodium acetate. (a) Product. Sodium acetate. (b) Conditions of use. This substance is...

  4. 21 CFR 582.1721 - Sodium acetate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Sodium acetate. 582.1721 Section 582.1721 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS....1721 Sodium acetate. (a) Product. Sodium acetate. (b) Conditions of use. This substance is...

  5. 21 CFR 582.1721 - Sodium acetate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Sodium acetate. 582.1721 Section 582.1721 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS....1721 Sodium acetate. (a) Product. Sodium acetate. (b) Conditions of use. This substance is...

  6. 21 CFR 582.1005 - Acetic acid.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Acetic acid. 582.1005 Section 582.1005 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS....1005 Acetic acid. (a) Product. Acetic acid. (b) Conditions of use. This substance is...

  7. 21 CFR 582.1005 - Acetic acid.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Acetic acid. 582.1005 Section 582.1005 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS....1005 Acetic acid. (a) Product. Acetic acid. (b) Conditions of use. This substance is...

  8. 21 CFR 582.1005 - Acetic acid.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Acetic acid. 582.1005 Section 582.1005 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS....1005 Acetic acid. (a) Product. Acetic acid. (b) Conditions of use. This substance is...

  9. 21 CFR 582.1005 - Acetic acid.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Acetic acid. 582.1005 Section 582.1005 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS....1005 Acetic acid. (a) Product. Acetic acid. (b) Conditions of use. This substance is...

  10. 21 CFR 582.1005 - Acetic acid.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Acetic acid. 582.1005 Section 582.1005 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS....1005 Acetic acid. (a) Product. Acetic acid. (b) Conditions of use. This substance is...

  11. 21 CFR 184.1185 - Calcium acetate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...known as acetate of lime or vinegar salts, is the calcium salt of acetic acid. It may be produced by the calcium hydroxide neutralization of acetic acid. (b) The ingredient meets the specifications of the Food Chemicals Codex, 3d Ed....

  12. 21 CFR 184.1185 - Calcium acetate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...known as acetate of lime or vinegar salts, is the calcium salt of acetic acid. It may be produced by the calcium hydroxide neutralization of acetic acid. (b) The ingredient meets the specifications of the Food Chemicals Codex, 3d Ed....

  13. 21 CFR 73.2396 - Lead acetate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2396 Lead acetate. (a...additive lead acetate may be safely used in cosmetics intended for coloring hair on the scalp...The amount of the lead acetate in the cosmetic shall be such that the lead...

  14. 21 CFR 73.2396 - Lead acetate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2396 Lead acetate. (a...additive lead acetate may be safely used in cosmetics intended for coloring hair on the scalp...The amount of the lead acetate in the cosmetic shall be such that the lead...

  15. 21 CFR 73.2396 - Lead acetate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2396 Lead acetate. (a...additive lead acetate may be safely used in cosmetics intended for coloring hair on the scalp...The amount of the lead acetate in the cosmetic shall be such that the lead...

  16. 21 CFR 522.2476 - Trenbolone acetate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Trenbolone acetate. 522.2476 Section 522.2476 Food... Trenbolone acetate. (a) Sponsors. See sponsors in § 510.600(c) of this chapter for use as in paragraph (d) of... days. (A) 140 milligrams (mg) trenbolone acetate (one implant consisting of 7 pellets, each...

  17. 21 CFR 522.2476 - Trenbolone acetate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Trenbolone acetate. 522.2476 Section 522.2476 Food... Trenbolone acetate. (a) Sponsors. See sponsors in § 510.600(c) of this chapter for use as in paragraph (d) of... days. (A) 140 milligrams (mg) trenbolone acetate (one implant consisting of 7 pellets, each...

  18. Cross-linked polyvinyl alcohol and method of making same

    NASA Technical Reports Server (NTRS)

    Hsu, L. C.; Sheibley, D. W.; Philipp, W. H. (inventors)

    1981-01-01

    A film-forming polyvinyl alcohol polymer is mixed with a polyaldehyde-polysaccharide cross-linking agent having at least two monosaccharide units and a plurality of aldehyde groups per molecule, perferably an average of at least one aldehyde group per monosaccharide units. The cross-linking agent, such as a polydialdehyde starch, is used in an amount of about 2.5 to 20% of the theoretical amount required to cross-link all of the available hydroxyl groups of the polyvinyl alcohol polymer. Reaction between the polymer and cross-linking agent is effected in aqueous acidic solution to produce the cross-linked polymer. The polymer product has low electrical resistivity and other properties rendering it suitable for making separators for alkaline batteries.

  19. Electrical conductivity of polyvinyl alcohol-multiwall carbon nanotubes composites

    NASA Astrophysics Data System (ADS)

    Amrin, Sayed; Deshpande, V. D.

    2013-06-01

    The dc and ac conductivity of polyvinyl alcohol (PVA)-multiwalled carbon nanotube (MWNT) nanocomposites prepared by solution casting were investigated by employing dielectric relaxation spectroscopy in broad frequency range (0.1 Hz-10 MHz) at room temperature as a function of the conductive weight fraction (p) ranging from 0 to 2wt.%. The frequency dependence of the measured conductivity obeys the universal dynamic response (UDR); a dc plateau followed, by the power law above a critical frequency (fc).

  20. Enzymatic production of glycerol acetate from glycerol.

    PubMed

    Oh, Seokhyeon; Park, Chulhwan

    2015-02-01

    In this study, we report the enzymatic production of glycerol acetate from glycerol and methyl acetate. Lipases are essential for the catalysis of this reaction. To find the optimum conditions for glycerol acetate production, sequential experiments were designed. Type of lipase, lipase concentration, molar ratio of reactants, reaction temperature and solvents were investigated for the optimum conversion of glycerol to glycerol acetate. As the result of lipase screening, Novozym 435 (Immobilized Candida antarctica lipase B) was turned out to be the optimal lipase for the reaction. Under the optimal conditions (2.5 g/L of Novozym 435, 1:40 molar ratio of glycerol to methyl acetate, 40 °C and tert-butanol as the solvent), glycerol acetate production was achieved in 95.00% conversion. PMID:25640720

  1. Stimuli-Responsive Mechanically Adaptive Polymer Nanocomposites

    PubMed Central

    Shanmuganathan, Kadhiravan; Capadona, Jeffrey R.; Rowan, Stuart J.; Weder, Christoph

    2010-01-01

    A new series of biomimetic stimuli-responsive nanocomposites, which change their mechanical properties upon exposure to physiological conditions, was prepared and investigated. The materials were produced by introducing percolating networks of cellulose nanofibers or “whiskers” derived from tunicates into poly(vinyl acetate) (PVAc), poly(butyl methacrylate) (PBMA), and blends of these polymers, with the objective of determining how the hydrophobicity and glass-transition temperature (Tg) of the polymer matrix affect the water-induced mechanically dynamic behavior. Below the Tg (~60–70 °C), the incorporation of whiskers (15.1 – 16.5% v/v) modestly increased the tensile storage moduli (E?) of the neat polymers from 0.6 to 3.8 GPa (PBMA) and from 2 to 5.2 GPa (PVAc). The reinforcement was much more dramatic above Tg, where E? increased from 1.2 to 690 MPa (PVAc) and ~1 to 1.1 GPa (PBMA). Upon exposure to physiological conditions (immersion in artificial cerebrospinal fluid, ACSF, at 37 °C) all materials displayed a decrease of E?. The most significant contrast was seen in PVAc; for example the E? of a 16.5% v/v PVAc/whisker nanocomposite decreased from 5.2 GPa to 12.7 MPa. Only a modest modulus decrease was measured for PBMA/whisker nanocomposite; here the E? of a 15.1% v/v PBMA/whisker nanocomposite decreased from 3.8 to 1.2 GPa. A systematic investigation revealed that the magnitude of the mechanical contrast was related to the degree of swelling with ACSF, which was shown to increase with whisker content, temperature, and polarity of the matrix (PVAc > PBMA). The mechanical morphing of the new materials can be described in the framework of both the percolation and Halpin-Kardos models for nanocomposite reinforcement, and is the result of changing interactions among the nanoparticles and plasticization of the matrix upon swelling. PMID:20305827

  2. Influence of the linkage type between the polymer backbone and side groups on the surface segregation of methyl groups during film formation.

    PubMed

    Zhang, Yizhi; Fan, Hao; Wang, Yuping; Zuo, Biao; Zhang, Wei; Wang, Shunli; Wang, Xinping

    2015-11-25

    Although poly(vinyl acetate) (PVAc) differs from poly(methyl acrylate) (PMA) only in the reversed position of the ester group, a large difference in the concentration dependence of the casting solution on the corresponding surface structure of the cast films of PVAc, PMA and poly(methyl methacrylate) (PMMA) was observed. The hydrophobicity of both PMA and PMMA films increased with increasing concentration of the corresponding polymer solution, whereas cast PVAc films showed the reverse trend. The surface structure of the cast films prepared with different concentrations of the casting solution, characterized by sum frequency generation (SFG) vibrational spectra, showed that the order of the methylene groups increased while that of the acetyl methyl group decreased on the surface of cast PVAc film with increasing concentration of casting solution. However, the order of the ester methyl group increased and that of methylene groups did not change for cast PMA films with increasing concentration of casting solution. The cast PMMA film showed a reverse trend compared with the corresponding PMA film. It is apparent that well-ordered ester or acetyl methyl groups on the surface, which are oriented away from the polymer film, rather than methylene groups, play an important role in determining surface hydrophobicity, as the latter shield the OC[double bond, length as m-dash]O groups of PVAc, PMA and PMMA film surfaces from being exposed, resulting in low surface free energy. The reason for this difference is attributed to the relatively low energy for ester methyl group reorientation, an ester group structure nearer to the trans state and more regular local configuration of segments in concentrated solutions of PMA and PMMA compared to that of PVAc. PMID:26415634

  3. Highly Stable and Tunable n-Type Graphene Field-Effect Transistors with Polyvinyl Alcohol Films

    E-print Network

    Maruyama, Shigeo

    1 Highly Stable and Tunable n-Type Graphene Field- Effect Transistors with Polyvinyl Alcohol Films@photon.t.u-tokyo.ac.jp ABSTRACT The intrinsic p-type behavior of graphene field-effect transistors (FETs) under ambient conditions. In this work, we present a protocol of tunable n-type doping of graphene FETs via polyvinyl alcohol (PVA

  4. 76 FR 42613 - National Emission Standards for Hazardous Air Pollutants for Polyvinyl Chloride and Copolymers...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-19

    ... for Hazardous Air Pollutants for Polyvinyl Chloride and Copolymers Production is being extended for 14 days. DATES: Comments. The public comment period for the proposed rule published May 20, 2011 (76 FR... Polyvinyl Chloride and Copolymers Production; Extension of Comment Period AGENCY: Environmental...

  5. 40 CFR 61.64 - Emission standard for polyvinyl chloride plants.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... chloride plants. 61.64 Section 61.64 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Standard for Vinyl Chloride § 61.64 Emission standard for polyvinyl chloride plants. An owner or operator of a polyvinyl chloride plant shall comply with the requirements of this section and § 61.65....

  6. 40 CFR 61.64 - Emission standard for polyvinyl chloride plants.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... chloride plants. 61.64 Section 61.64 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Standard for Vinyl Chloride § 61.64 Emission standard for polyvinyl chloride plants. An owner or operator of a polyvinyl chloride plant shall comply with the requirements of this section and § 61.65....

  7. 40 CFR 61.64 - Emission standard for polyvinyl chloride plants.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... chloride plants. 61.64 Section 61.64 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Standard for Vinyl Chloride § 61.64 Emission standard for polyvinyl chloride plants. An owner or operator of a polyvinyl chloride plant shall comply with the requirements of this section and § 61.65....

  8. 40 CFR 61.64 - Emission standard for polyvinyl chloride plants.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... chloride plants. 61.64 Section 61.64 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Standard for Vinyl Chloride § 61.64 Emission standard for polyvinyl chloride plants. An owner or operator of a polyvinyl chloride plant shall comply with the requirements of this section and § 61.65....

  9. 40 CFR 61.64 - Emission standard for polyvinyl chloride plants.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ..., may not exceed: (i) 2000 ppm for polyvinyl chloride dispersion resins, excluding latex resins; (ii) 400 ppm for all other polyvinyl chloride resins, including latex resins, averaged separately for each..., excluding latex resins, with the product determined on a dry solids basis; (ii) 0.4 g/kg (0.8...

  10. Positron scattering from vinyl acetate

    NASA Astrophysics Data System (ADS)

    Chiari, L.; Zecca, A.; Blanco, F.; García, G.; Brunger, M. J.

    2014-09-01

    Using a Beer-Lambert attenuation approach, we report measured total cross sections (TCSs) for positron scattering from vinyl acetate (C4H6O2) in the incident positron energy range 0.15-50 eV. In addition, we also report an independent atom model with screening corrected additivity rule computation results for the TCSs, differential and integral elastic cross sections, the positronium formation cross section and inelastic integral cross sections. The energy range of these calculations is 1-1000 eV. While there is a reasonable qualitative correspondence between measurement and calculation for the TCSs, in terms of the energy dependence of those cross sections, the theory was found to be a factor of ˜2 larger in magnitude at the lower energies, even after the measured data were corrected for the forward angle scattering effect.

  11. Extractive fermentation of acetic acid

    SciTech Connect

    Busche, R.M.

    1991-12-31

    In this technoeconomic evaluation of the manufacture of acetic acid by fermentation, the use of the bacterium: Acetobacter suboxydans from the old vinegar process was compared with expected performance of the newer Clostridium thermoaceticum bacterium. Both systems were projected to operate as immobilized cells in a continuous, fluidized bed bioreactor, using solvent extraction to recover the product. Acetobacter metabolizes ethanol aerobically to produce acid at 100 g/L in a low pH medium. This ensures that the product is in the form of a concentrated extractable free acid, rather than as an unextractable salt. Unfortunately, yields from glucose by way of the ethanol fermentation are poor, but near the biological limits of the organisms involved. Conversely, C. thermoaceticum is a thermophilic anaerobe that operates at high fermentation rates on glucose at neutral pH to produce acetate salts directly in substantially quantitative yields. However, it is severely inhibited by product, which restricts concentration to a dilute 20 g/L. An improved Acetobacter system operating with recycled cells at 50 g/L appears capable of producing acid at $0.38/lb, as compared with a $0.29/lb price for synthetic acid. However, this system has only a limited margin for process improvement. The present Clostridium system cannot compete, since the required selling price would be $0.42/lb. However, if the organism could be adapted to tolerate higher product concentrations at acid pH, selling price could be reduced to $0.22/lb, or about 80% of the price of synthetic acid.

  12. Preparation and application of low molecular weight poly(vinyl chloride). III mechanical properties of blended poly(vinyl chloride)

    SciTech Connect

    Yamamoto, Kikuo; Maehala, Takashi; Mitani, Katsuo; Mizutani, Yukio )

    1993-11-05

    The blending effect of poly(vinyl chloride) with relatively higher molecular weight (HMW-PVC) and relatively lower molecular weight (LMW-PVC) has been investigated by measuring various mechanical properties: melt properties, tensile strength, tensile modulus, and impact strength. The blended PVC has slightly improved melt properties in comparison with the HMW-PVC used. The tensile strength of the blended PVC is related to the weight-average polymerization degree (Pw) of LMW-PVC and the LMW-PVC content. At the LMW-PVC content of 20%, the tensile strength of blended PVC is a maximum: approximately 58 MPa.

  13. Manufacturing Ethyl Acetate From Fermentation Ethanol

    NASA Technical Reports Server (NTRS)

    Rohatgi, Naresh K.; Ingham, John D.

    1991-01-01

    Conceptual process uses dilute product of fermentation instead of concentrated ethanol. Low-concentration ethanol, extracted by vacuum from fermentation tank, and acetic acid constitutes feedstock for catalytic reaction. Product of reaction goes through steps that increases ethyl acetate content to 93 percent by weight. To conserve energy, heat exchangers recycle waste heat to preheat process streams at various points.

  14. 21 CFR 73.2396 - Lead acetate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2396 Lead acetate. (a) Identity. The color additive lead... cosmetics intended for coloring hair on the scalp only, subject to the following restrictions: (1) The amount of the lead acetate in the cosmetic shall be such that the lead content, calculated as Pb,...

  15. 21 CFR 73.2396 - Lead acetate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2396 Lead acetate. (a) Identity. The color additive lead... cosmetics intended for coloring hair on the scalp only, subject to the following restrictions: (1) The amount of the lead acetate in the cosmetic shall be such that the lead content, calculated as Pb,...

  16. 21 CFR 73.2396 - Lead acetate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2396 Lead acetate. (a) Identity. The color additive lead... cosmetics intended for coloring hair on the scalp only, subject to the following restrictions: (1) The amount of the lead acetate in the cosmetic shall be such that the lead content, calculated as Pb,...

  17. 21 CFR 73.2396 - Lead acetate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2396 Lead acetate. (a) Identity. The color additive lead... cosmetics intended for coloring hair on the scalp only, subject to the following restrictions: (1) The amount of the lead acetate in the cosmetic shall be such that the lead content, calculated as Pb,...

  18. 21 CFR 73.2396 - Lead acetate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2396 Lead acetate. (a) Identity. The color additive lead... cosmetics intended for coloring hair on the scalp only, subject to the following restrictions: (1) The amount of the lead acetate in the cosmetic shall be such that the lead content, calculated as Pb,...

  19. CORROSION OF LEAD SHIELDING IN NUCLEAR MATERIALS PACKAGES

    SciTech Connect

    Subramanian, K; Kerry Dunn, K; Joseph Murphy, J

    2008-07-18

    Inspection of United States-Department of Energy (US-DOE) model 9975 nuclear materials shipping package revealed corrosion of the lead shielding that was induced by off-gas constituents from organic components in the package. Experiments were performed to determine the corrosion rate of lead when exposed to off-gas or degradation products of these organic materials. The results showed that the room temperature vulcanizing (RTV) sealant was the most corrosive organic species used in the construction of the packaging, followed by polyvinyl acetate (PVAc) glue. Fiberboard material, also used in the construction of the packaging induced corrosion to a much lesser extent than the PVAc glue and RTV sealant, and only in the presence of condensed water. The results indicated faster corrosion at temperatures higher than ambient and with condensed water. In light of these corrosion mechanisms, the lead shielding was sheathed in a stainless steel liner to mitigate against corrosion.

  20. CORROSION OF LEAD SHIELDING IN NUCLEAR MATERIALS PACKAGES

    SciTech Connect

    Subramanian, K; Kerry Dunn, K

    2007-11-16

    Inspection of United States-Department of Energy (US-DOE) model 9975 nuclear materials shipping package revealed corrosion of the lead shielding induced by off-gas constituents from organic components in the package. Experiments were performed to determine the corrosion rate of lead when exposed to off-gas or degradation products of these organic materials. The results showed that the room temperature vulcanizing (RTV) sealant was the most corrosive organic species followed by the polyvinyl acetate (PVAc) glue. The fiberboard material induced corrosion to a much lesser extent than the PVAc glue and RTV, and only in the presence of condensed water. The results indicated faster corrosion at temperatures higher than ambient and with condensed water as expected. A corrosion rate of 0.05 mm/year measured for coupons exposed to the most aggressive conditions was recommended as a conservative estimate for use in package performance calculations.

  1. 21 CFR 582.5933 - Vitamin A acetate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...2010-04-01 2010-04-01 false Vitamin A acetate. 582.5933 Section 582...AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5933 Vitamin A acetate. (a) Product. Vitamin A acetate. (b) Conditions of...

  2. Soluplus Graft Copolymer: Potential Novel Carrier Polymer in Electrospinning of Nanofibrous Drug Delivery Systems for Wound Therapy

    PubMed Central

    Tamm, Ingrid; Laidmäe, Ivo; Lust, Andres; Kirsimäe, Kalle

    2014-01-01

    Electrospinning is an effective method in preparing polymeric nanofibrous drug delivery systems (DDSs) for topical wound healing and skin burn therapy applications. The aim of the present study was to investigate a new synthetic graft copolymer (Soluplus) as a hydrophilic carrier polymer in electrospinning of nanofibrous DDSs. Soluplus (polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer (PCL-PVAc-PEG)) was applied in the nonwoven nanomats loaded with piroxicam (PRX) as a poorly water-soluble drug. Raman spectroscopy, X-ray powder diffraction, differential scanning calorimetry, and scanning electron microscopy (SEM) were used in the physical characterization of nanofibrous DDSs. According to the SEM results, the drug-loaded PCL-PVAc-PEG nanofibers were circular in cross-section with an average diameter ranging from 500?nm up to 2?µm. Electrospinning stabilized the amorphous state of PRX. In addition, consistent and sustained-release profile was achieved with the present nanofibrous DDSs at the physiologically relevant temperature and pH applicable in wound healing therapy. In conclusion, electrospinning can be used to prepare nanofibrous DDSs of PCL-PVAc-PEG graft copolymer (Soluplus) and to stabilize the amorphous state of a poorly water-soluble PRX. The use of this synthetic graft copolymer can open new options to formulate nanofibrous DDSs for wound healing. PMID:24575414

  3. New insight into modified release pellets - Internal structure and drug release mechanism.

    PubMed

    Ensslin, Simon; Moll, Klaus Peter; Paulus, Kurt; Mäder, Karsten

    2008-06-01

    The aim of the study was to explore the drug release mechanism from pellets, coated with blends of poly(vinyl acetate) (PVAc) and polyvinyl alcohol-polyethylene glycol graft copolymer (PVA-PEG). Water influx and drug solubilization inside the pellets were investigated in correlation to drug release. The highly soluble drug Chlorpheniramine maleate (CPM) was used as a model compound. Modified release pellets were manufactured by fluid bed drug layering and film coating of starter beads. The pellets were characterized using cross section EDX mapping, confirming location and homogeneity of the different layers. A film coat of 23%, containing PVAc/PVA-PEG in 9:1 ratio, resulted in a sigmoid shaped release curve with 2 h lag-time, followed by 3 h of continuous drug release. Using NMR analysis, water influx and drug solubilization inside the pellets were detected within 20 min. Additionally, dissolution of PVA-PEG after several minutes and drug release after the lag-time were measurable. A fast water influx into PVAc/PVA-PEG film coated pellets did not result in a fast drug release. Despite a fast drug solubilization within the pellets, drug release was initiated after 2 h, suggesting a one way stream of water during the observed lag-time. PMID:18433911

  4. Highly sensitive pseudo-differential ac-nanocalorimeter for the study of the glass transition

    NASA Astrophysics Data System (ADS)

    Laarraj, Mohcine; Adhiri, Rahma; Ouaskit, Said; Moussetad, Mohamed; Guttin, Christophe; Richard, Jacques; Garden, Jean-Luc

    2015-11-01

    We present a nanocalorimeter designed for the measurement of the dynamic heat capacity of thin films. The microfabricated sensor, the thermal conditioning of the sensor, as well as the highly stable and low noise electronic chain allow measurements of the real and imaginary parts of the complex specific heat with a resolution ? C/C of about 10-5. The performances of this quasi-differential nanocalorimeter were tested on a model of polymeric glass-former, the polyvinyl acetate (PVAc). The high stability and low noise of the device are essential for accurate studies on non-equilibrium slow relaxing systems such as glasses.

  5. Cross-linked polyvinyl alcohol films as alkaline battery separators

    NASA Technical Reports Server (NTRS)

    Sheibley, D. W.; Manzo, M. A.; Gonzalez-Sanabria, O. D.

    1982-01-01

    Cross-linking methods were investigated to determine their effect on the performance of polyvinyl alcohol (PVA) films as alkaline battery separators. The following types of cross-linked PVA films are discussed: (1) PVA-dialdehyde blends post-treated with an acid or acid periodate solution (two-step method) and (2) PVA-dialdehyde blends cross-linked during film formation (drying) by using a reagent with both aldehyde and acid functionality (one-step method). Laboratory samples of each cross-linked type of film were prepared and evaluated in standard separator screening tests. The pilot-plant batches of films were prepared and compared to measure differences due to the cross-linking method. The pilot-plant materials were then tested in nickel oxide - zinc cells to compare the two methods with respect to performance characteristics and cycle life. Cell test results are compared with those from tests with Celgard.

  6. Cross-linked polyvinyl alcohol films as alkaline battery separators

    NASA Technical Reports Server (NTRS)

    Sheibley, D. W.; Manzo, M. A.; Gonzalez-Sanabria, O. D.

    1983-01-01

    Cross-linking methods have been investigated to determine their effect on the performance of polyvinyl alcohol (PVA) films as alkaline battery separators. The following types of cross-linked PVA films are discussed: (1) PVA-dialdehyde blends post-treated with an acid or acid periodate solution (two-step method) and (2) PVA-dialdehyde blends cross-linked during film formation (drying) by using a reagent with both aldehyde and acid functionality (one-step method). Laboratory samples of each cross-linked type of film were prepared and evaluated in standard separator screening tests. Then pilot-plant batches of films were prepared and compared to measure differences due to the cross-linking method. The pilot-plant materials were then tested in nickel oxide-zinc cells to compare the two methods with respect to performance characteristics and cycle life. Cell test results are compared with those from tests with Celgard.

  7. Polyvinyl alcohol coating of polystyrene inertial confinement fusion targets

    NASA Technical Reports Server (NTRS)

    Annamalai, P.; Lee, M. C.; Crawley, R. L.; Downs, R. L.

    1985-01-01

    An inertial confinement fusion (ICF) target made of polystyrene is first levitated in an acoustic field. The surface of the target is then etched using an appropriate solution (e.g., cyclohexane) to enhance the wetting characteristics. A specially prepared polyvinyl alcohol solution is atomized using an acoustic atomizer and deposited on the surface of the target. The solution is air dried to form a thin coating (2 microns) on the target (outside diameter of about 350-850 microns). Thicker coatings are obtained by repeated applications of the coating solutions. Preliminary results indicate that uniform coatings may be achievable on the targets with a background surface smoothness in the order of 1000 A.

  8. Preparation and characterization of bioglass/polyvinyl alcohol composite hydrogel.

    PubMed

    Xu, Hong; Wang, Yingjun; Zheng, Yudong; Chen, Xiaofeng; Ren, Li; Wu, Gang; Huang, Xiaoshan

    2007-06-01

    In order to form firm active fixation with the adjacent bone, a new kind of bioactive composite hydrogel was prepared with polyvinyl alcohol (PVA) and bioglass (BG) through ultrasonic dispersion, heat-high-pressure and freeze/thawed technique. A digital speckle correlation method (DSCM) was utilized to characterize the mechanical properties of the series of BG/PVA composites. Results showed that at different load pressures, the composite hydrogel displayed different displacement and deformation in the V field. Results also showed that an increase of PVA percentage (15-30 wt%) or of bioglass percentage (2-10 wt%) in composite hydrogel could lead to an increase in the elastic compression modulus. Scanning electron microscope results indicated that bioglass was uniformly dispersed in the BG/PVA composite hydrogel. The BG/PVA composite hydrogel shows a promising prospect as a new bionic cartilage implantation material. PMID:18458437

  9. End-of-life of starch-polyvinyl alcohol biopolymers.

    PubMed

    Guo, M; Stuckey, D C; Murphy, R J

    2013-01-01

    This study presents a life cycle assessment (LCA) model comparing the waste management options for starch-polyvinyl alcohol (PVOH) biopolymers including landfill, anaerobic digestion (AD), industrial composting and home composting. The ranking of biological treatment routes for starch-PVOH biopolymer wastes depended on their chemical compositions. AD represents the optimum choice for starch-PVOH biopolymer containing N and S elements in global warming potential (GWP(100)), acidification and eutrophication but not on the remaining impact categories, where home composting was shown to be a better option due to its low energy and resource inputs. For those starch-PVOH biopolymers with zero N and S contents home composting delivered the best environmental performance amongst biological treatment routes in most impact categories (except for GWP(100)). The landfill scenario performed generally well due largely to the 100-year time horizon and efficient energy recovery system modeled but this good performance is highly sensitive to assumptions adopted in landfill model. PMID:23131650

  10. Hemocompatibility study of a bacterial cellulose/polyvinyl alcohol nanocomposite.

    PubMed

    Leitão, Alexandre F; Gupta, Swati; Silva, João Pedro; Reviakine, Ilya; Gama, Miguel

    2013-11-01

    Bacterial cellulose (BC) has been suggested to be a suitable biomaterial for the development of cardiovascular grafts. The combination of BC with polyvinyl alcohol (PVA) results in nanocomposites with improved properties. Surprisingly, there are very few studies on the BC-blood interaction. This is the focus of this paper. We present the first thorough assessment of the hemocompatibility of the BC/PVA nanocomposite. Whole blood clotting time, plasma recalcification, Factor XII activation, platelet adhesion and activation, hemolytic index and complement activation are all determined. The platelet activation profiles on BC and BC/PVA surfaces are comprehensively characterized. BC and BC/PVA outperformed ePTFE--used as a point of comparison--thus evidencing their suitability for cardiovascular applications. PMID:23880088

  11. Estimation of mechanochemical dechlorination rate of poly(vinyl chlorde).

    PubMed

    Mio, Hiroshi; Saeki, Shu; Kano, Junya; Saito, Fumio

    2002-03-15

    Poly(vinyl chloride) (PVC) was ground in air with CaO in the presence of quartz powder as a grinding aid by a small-scale planetary ball mill to investigate the relation of the dechlorination rate of PVC with the impact energy of the balls calculated from a computer simulation based on the Discrete Element Method under various conditions. Mechanochemical dechlorination proceeds as the grinding progresses and is improved with an increase in both the mill speed and the amount of balls introduced into the mill. The same trend can be seen in the relation between the specific normal impact energy of the balls and the rotational speed. The relationship between the observed dechlorination rate and the computed normal impact energy of the balls is linear, with a correlation coefficient of 0.965. This relationship can be used to estimate the dechlorination rate of PVC in a large-scale planetary ball mill. PMID:11944691

  12. Evaluation of a Polyvinyl Toluene Neutron Counter Array

    SciTech Connect

    Robert Hayes

    2008-03-01

    The purpose of this article is to simulate the performance of a neutron detector array for empirical configuration optimization and preliminary algorithm evaluation. Utilizing a compact array of borated Polyvinyl Toluene light pipes and Photomultiplier Tubes, pulse shape analysis, standard spectral histogramming, and multiplicity counting can enable neutron measurements for multiple applications. Results demonstrate that analysis with Monte Carlo N-Particle (MCNP) can be used to obtain a better understanding of field measurement results and aid in algorithm development for unfolding in conjunction with detector optimization. Use of a handheld neutron spectrometer has promise of widespread applicability. By correlating MCNP results with empirical measurements, substantial confidence can be placed on predicting detector response to sufficiently similar spectral sources under alternate experimental configurations. In addition, use of the detector has substantial promise for operational health physics applications.

  13. Biodegradable thermoplastic composites based on polyvinyl alcohol and algae.

    PubMed

    Chiellini, Emo; Cinelli, Patrizia; Ilieva, Vassilka I; Martera, Martina

    2008-03-01

    Algae constitute a largely available, low value material from renewable resources of marine origin to be used for the production of eco-compatible composites. Fibers of the green alga Ulva armoricana from the French coast were positively evaluated for the production of composites with a hydrophilic, eco-compatible polymer, such as poly(vinyl alcohol) (PVA) as continuous matrix by casting of aqueous suspensions and compression molding. PVA, Ulva, and starch were also successfully processed by the melt in the presence of glycerol. Positive results were obtained for film-forming properties and mechanical characteristics also with limited amounts of PVA (40%) attesting for Ulva suitability to be introduced in composites (up to 30%). Degradation in soil of Ulva and an Ulva-based composites outlined a rapid mineralization of Ulva in the selected medium (over 80% in 100 days) while the composite samples underwent a mineralization rate affected by the different component propensity to degradation. PMID:18257530

  14. Silver Nanoparticle Fabrication by Laser Ablation in Polyvinyl Alcohol Solutions

    NASA Astrophysics Data System (ADS)

    Halimah Mohamed., K.; Mahmoud Goodarz, Naseri; Amir, Reza Sadrolhosseini; Arash, Dehzangi; Ahmad, Kamalianfar; Elias, B. Saion; Reza, Zamiri; Hossein Abastabar, Ahangar; Burhanuddin, Y. Majlis

    2014-07-01

    A laser ablation technique is applied for synthesis of silver nanoparticles in different concentrations of polyvinyl alcohol (PVA) aqueous solution. The ablation of high pure silver plate in the solution is carried out by a nanosecond Q-switched Nd:YAG pulsed laser. X-ray diffraction and transmission electron microscopy are implemented to explore the particles sizes. The effects of PVA concentrations on the absorbance of the silver nanoparticles are studied as well, by using a UV-vis spectrophotometer. The preparation process is carried out for deionized water as a reference sample. The comparison of the obtained results with the reference sample shows that the formation efficiency of nanoparticles in PVA is much higher and the sizes of particles are also smaller.

  15. Immobilization of Enzyme into Poly(vinyl alcohol) Membrane.

    PubMed

    Imai, K; Shiomi, T; Uchida, K; Miya, M

    1986-11-01

    Glucoamylase, invertase, and cellulase were entrapped within poly(vinyl alcohol) (PVA) membrane cross-linked by means of irradiation of ultraviolet light. The conditions for immobilization of glucoamylase were examined with respect to enzyme concentration in PVA, sensitizer (sodium benzoate) concentration in PVA, irradiation time, and membrane thickness. Various characteristics of immobilized glucoamylase were evaluated. Among them, the pH activity curve for the immobilized enzyme was superior to that for the native one, and thermal stability was improved by immobilization with bovine albumin. The apparent K(m) was larger for immobilized glucoamylase than for the native one, while V(max) was smaller for the immobilized enzyme. Also, the apparent K(m) appeared to be affected by the molecular size of the substrate. Further, immobilized invertase and cellulase showed good stabilities in repeating usage. PMID:18555286

  16. The pharmacology of nomegestrol acetate.

    PubMed

    Ruan, Xiangyan; Seeger, Harald; Mueck, Alfred O

    2012-04-01

    Nomegestrol acetate (NOMAC) is a 19-norprogesterone derivative with high biological activity at the progesterone receptor, a weak anti-androgenic effect, but with no binding to estrogen, glucocorticoid or mineralocorticoid receptors. At dosages of 1.5mg/day or more, NOMAC effectively suppresses gonadotropic activity and ovulation in women of reproductive age. Hemostasis, lipids and carbohydrate metabolism remain largely unchanged. In normal and cancerous human breast cells, NOMAC has shown favorable effects on estrogen metabolism. Like natural progesterone (but in contrast to some other synthetic progestogens), it does not appear stimulate the proliferation of cancerous breast cells. While there has been some experience of the use of NOMAC in combination with estrogens as a hormone replacement therapy, most of the data on the compound are reported in the context of its inclusion as a component of a new contraceptive pill comprising 2.5mg NOMAC combined with 1.5mg estradiol. Because of its strong endometrial efficacy, and due to its high antigonadotropic activity and long elimination half-life (about 50h), the contraceptive efficacy of the new pill is maintained even when dosages are missed. Furthermore, for the first time with a monophasic 24/4 regimen containing estradiol, cyclical stability can be achieved comparable with that obtained using pills containing ethinyl estradiol and progestogens like levonorgestrel or drospirenone. The addition of NOMAC to estradiol means that the beneficial effects of estrogen are not lost, which is of especial importance in relation to the cardiovascular system. On the basis both of its pharmacology and of studies performed during the development of the NOMAC/estradiol pill, involving some 4000 women in total, good long-term tolerability can be expected for NOMAC, although its safety profile is still to be fully ascertained, as the clinical endpoint studies are yet to be completed. PMID:22364709

  17. 21 CFR 522.1073 - Gonadorelin acetate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS § 522.1073 Gonadorelin acetate. (a) Specifications. Each...

  18. Concentrating aqueous acetate solutions with tertiary amines 

    E-print Network

    Lee, Champion

    1993-01-01

    was originally applied to water desalination in which water was extracted from aqueous sodium chloride solutions. Here, we explore its potential to recover acetate produced via fermentation. At 40C 55C, which corresponds to typical fen-fermentation temperatures...

  19. Acetic Acid Off Gassing in Clamshell Enclosures

    E-print Network

    Brewer, Allison

    2013-01-01

    . This presentation will investigate the use of acid detection strips (A-D strips) to study acetic acid off gassing occurring in custom-made, cloth covered book boxes constructed and used by conservators in research libraries....

  20. Fragrance material review on 4-methylbenzyl acetate.

    PubMed

    McGinty, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of 4-methylbenzyl acetate when used as a fragrance ingredient is presented. 4-Methylbenzyl acetate is a member of the fragrance structural group Aryl Alkyl Alcohol Simple Acid Esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for 4-methylbenzyl acetate were evaluated, then summarized, and includes: physical properties, skin irritation, skin sensitization, and elicitation data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22414643

  1. Fragrance material review on 3-phenylpropyl acetate.

    PubMed

    McGinty, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of 3-phenylpropyl acetate when used as a fragrance ingredient is presented. 3-Phenylpropyl acetate is a member of the fragrance structural group Aryl Alkyl Alcohol Simple Acid Esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for 3-phenylpropyl acetate were evaluated, then summarized, and includes: physical properties, acute toxicity, skin irritation, skin sensitization, and toxicokinetics data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Please refer to Belsito et al., 2012 for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22414651

  2. Fragrance material review on anisyl acetate.

    PubMed

    McGinty, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of anisyl acetate when used as a fragrance ingredient is presented. Anisyl acetate is a member of the fragrance structural group Aryl Alkyl Alcohol Simple Acid Esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for anisyl acetate were evaluated, then summarized, and includes: physical properties, skin irritation, skin sensitization, elicitation, and phototoxicity data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Please refer to Belsito et al., 2012 for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22414654

  3. [carbonyl-11 C]Benzyl acetate: Automated

    E-print Network

    Pike, Victor W.

    Fujita,a Osamu Inoue,b Robert B. Innis,a and Victor W. Pikea [carbonyl-11 C]Benzyl acetate ([11 C]1) has, so increasing the difficulty of their use in small-scale automated radiochemistry. Organolithium

  4. Activation of methyl acetate on Pd(111)

    NASA Astrophysics Data System (ADS)

    Xu, Lijun; Xu, Ye

    2010-06-01

    The adsorption and activation of methyl acetate (CH 3COOCH 3), one of the simplest carboxylic esters, on Pd(111) have been studied using self-consistent periodic density functional theory calculations. Methyl acetate adsorbs weakly through the carbonyl oxygen. Its activation occurs via dehydrogenation, instead of direct C-O bond dissociation, on clean Pd(111): It is much more difficult to dissociate the C-O bonds ( Ea ? 2.0 eV for the carbonyl and acetate-methyl bonds; Ea = 1.0 eV for the acetyl-methoxy bond) than to dissociate the C-H bonds to produce enolate (CH 2COOCH 3; Ea = 0.74 eV) or methylene acetate (CH 3COOCH 2; Ea = 0.82 eV). The barriers for C-H and C-O bond dissociation are directly calculated for enolate and methylene acetate, and estimated for further dehydrogenated derivatives (CH 3COOCH, CH 2COOCH 2, and CHCOOCH 3) based on the Brønsted-Evans-Polanyi linear energy relations formed by the calculated steps. The enolate pathway leads to successive dehydrogenation to CCOOCH 3, whereas methylene acetate readily dissociates to yield acetyl. The selectivity for dissociating the acyl-alkoxy C-O bond, which is desired for alcohol formation, is therefore fundamentally limited by the facility of dehydrogenation under vacuum/low-pressure conditions on Pd(111).

  5. Hydrogen-bonded layer-by-layer assembly of poly(vinyl alcohol) and tannic acid

    E-print Network

    Sample, Caitlin (Caitlin Sarah)

    2014-01-01

    Hydrogen-bonded multilayer thin films containing tannic acid (TA) and poly(vinyl alcohol) (PVA) were assembled under different pH conditions, and film growth and dissolution behavior was assessed through profilometry. ...

  6. Structural studies of alumina pillared hectorite using polyvinyl alcohol as a pillaring agent 

    E-print Network

    Kroenig, Andrea N

    1997-01-01

    In the present work, the structures of a natural hectorite clay pillared with alumina were studied. Frequently, polyvinyl alcohol (PVA) was added as a pillaring agent to observe structural differences in the calcined ...

  7. Organically crosslinked polyvinyl alcohol copolymetric gels for use under harsh reservoir conditions

    SciTech Connect

    Haskin, D.H.; Shu, P.

    1990-07-10

    This patent describes a process for recovering oil from a subterranean oil-bearing formation having relatively high permeability zones and relatively low permeability zones penetrated by at least one production well in fluid communication with a substantial portion of the formation. It comprises: injecting into the formation an aqueous gel-forming composition comprising water, a water-dispersible polyvinyl alcohol copolymer, the polyvinyl alcohol copolymer selected from the group consisting of copolymers of vinyl alcohol and vinyl alkyl sulfonate either.

  8. Direct Detection of the Acetate-forming Activity of the Enzyme Acetate Kinase

    PubMed Central

    Fowler, Matthew L.; Ingram-Smith, Cheryl J.; Smith, Kerry S.

    2011-01-01

    Acetate kinase, a member of the acetate and sugar kinase-Hsp70-actin (ASKHA) enzyme superfamily1-5, is responsible for the reversible phosphorylation of acetate to acetyl phosphate utilizing ATP as a substrate. Acetate kinases are ubiquitous in the Bacteria, found in one genus of Archaea, and are also present in microbes of the Eukarya6. The most well characterized acetate kinase is that from the methane-producing archaeon Methanosarcina thermophila7-14. An acetate kinase which can only utilize PPi but not ATP in the acetyl phosphate-forming direction has been isolated from Entamoeba histolytica, the causative agent of amoebic dysentery, and has thus far only been found in this genus15,16. In the direction of acetyl phosphate formation, acetate kinase activity is typically measured using the hydroxamate assay, first described by Lipmann17-20, a coupled assay in which conversion of ATP to ADP is coupled to oxidation of NADH to NAD+ by the enzymes pyruvate kinase and lactate dehydrogenase21,22, or an assay measuring release of inorganic phosphate after reaction of the acetyl phosphate product with hydroxylamine23. Activity in the opposite, acetate-forming direction is measured by coupling ATP formation from ADP to the reduction of NADP+ to NADPH by the enzymes hexokinase and glucose 6-phosphate dehydrogenase24. Here we describe a method for the detection of acetate kinase activity in the direction of acetate formation that does not require coupling enzymes, but is instead based on direct determination of acetyl phosphate consumption. After the enzymatic reaction, remaining acetyl phosphate is converted to a ferric hydroxamate complex that can be measured spectrophotometrically, as for the hydroxamate assay. Thus, unlike the standard coupled assay for this direction that is dependent on the production of ATP from ADP, this direct assay can be used for acetate kinases that produce ATP or PPi. PMID:22214984

  9. Acetylation of Starch with Vinyl Acetate in Imidazolium Ionic Liquids and Characterization of Acetate Distribution

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Starch was acetylated with vinyl acetate in different 1-butyl-3-methylimidazolium (BMIM) salts as solvent in effort to produce starches with different acetylation patterns. Overall degree of substitution was much higher for basic anions such as acetate and dicyanimide (dca) than for neutral anions ...

  10. Tested Demonstrations: Buffer Capacity of Various Acetic Acid-Sodium Acetate Systems: A Lecture Experiment.

    ERIC Educational Resources Information Center

    Donahue, Craig J.; Panek, Mary G.

    1985-01-01

    Background information and procedures are provided for a lecture experiment which uses indicators to illustrate the concept of differing buffer capacities by titrating acetic acid/sodium acetate buffers with 1.0 molar hydrochloric acid and 1.0 molar sodium hydroxide. A table with data used to plot the titration curve is included. (JN)

  11. Thermal stability of polyvinyl alcohol/nanocrystalline cellulose composites.

    PubMed

    Voronova, Marina I; Surov, Oleg V; Guseinov, Sabir S; Barannikov, Vladimir P; Zakharov, Anatoly G

    2015-10-01

    Thermal stability of polyvinyl alcohol/cellulose nanocrystals (PVA/CNCs) composites prepared with solution casting technique was studied. The PVA/CNCs composites were characterized by Fourier transform infrared spectrometry, X-ray diffraction, differential scanning calorimeter (DSC) and thermogravimetric (TG) analysis. Due to the presence of CNCs nanoparticles, thermal degradation of the composites occurs at much higher temperatures compared to that of the neat PVA. Thermal stability of the PVA/CNCs composites is maximally enhanced with CNCs content of 8-12 wt%. Some thermal degradation products of the PVA/CNCs composites were identified by mass spectrometric analysis. TG measurements with synchronous recording of mass spectra revealed that the thermal degradation of both CNCs and PVA in the composites with CNCs content of 8-12 wt% occurs simultaneously at a much higher temperature than that of CNCs or the neat PVA. However, with increasing CNCs content more than 12 wt% the thermal stability of the composites decreases. In this case, the degradation of CNCs comes first followed by the degradation of PVA. PMID:26076645

  12. UV-responsive polyvinyl alcohol nanofibers prepared by electrospinning

    NASA Astrophysics Data System (ADS)

    Khatri, Zeeshan; Ali, Shamshad; Khatri, Imran; Mayakrishnan, Gopiraman; Kim, Seong Hun; Kim, Ick-Soo

    2015-07-01

    We report UV-responsive polyvinyl alcohol (PVA) nanofibers for potential application for recording and erasing quick response (QR) codes. We incorporate 1?-3?-dihydro-8-methoxy-1?,3?,3?-trimethyl-6-nitrospiro [2H-1-benzopyran-2,2?-(2H)-indole] (indole) and,3-dihydro-1,3,3-trimethylspiro [2H-indole-2,3?-[3H] phenanthr [9,10-b] (1,4) oxazine] (oxazine) into PVA polymer matrix via electrospinning technique. The resultant nanofibers were measured for recording-erasing, photo-coloration and thermal reversibility. The rate of photo-coloration of PVA-indole nanofibers was five times higher than the PVA-oxazine nanofibers, whereas the thermal reversibility found to be more than twice as fast as PVA-oxazine nanofibers. Results showed that the resultant nanofibers have very good capability of recording QR codes multiple times. The FTIR spectroscopy and SEM were employed to characterize the electrospun nanofibers. The UV-responsive PVA nanofibers have great potentials as a light-driven nanomaterials incorporated within sensors, sensitive displays and in optical devices such as erasable and rewritable optical storage.

  13. Quantifying the lubricity of mechanically tough polyvinyl alcohol hydrogels for cartilage repair.

    PubMed

    Ling, Doris; Bodugoz-Senturk, Hatice; Nanda, Salil; Braithwaite, Gavin; Muratoglu, Orhun K

    2015-12-01

    Polyvinyl alcohol hydrogels are biocompatible and can be used as synthetic articular cartilage. Their mechanical characteristics can be tailored by various techniques such as annealing or blending with other hydrophilic polymers. In this study, we quantified the coefficient of friction of various candidate polyvinyl alcohol hydrogels against cobalt-chrome alloy or swine cartilage using a new rheometer-based method. We investigated the coefficient of friction of polyvinyl alcohol-only hydrogels and blends with polyethylene glycol, polyacrylic acid, and polyacrylamide against swine cartilage and polished cobalt-chrome surfaces. The addition of the functional groups to polyvinyl alcohol, such as acrylamide (semi-interpenetrating network) and acrylic acid (blend), significantly reduced the coefficient of friction. The coefficient of friction of the polyvinyl alcohol-only hydrogel was measured as 0.4 ± 0.03 against cobalt-chrome alloy, and 0.09 ± 0.004 against cartilage, while those measurements for the polyvinyl alcohol-polyacrylic acid blends and polyvinyl alcohol-polyacrylamide semi-interpenetrating network were 0.07 ± 0.01 and 0.1 ± 0.003 against cobalt-chrome alloy, and 0.03 ± 0.001 and 0.02 ± 0.001 against cartilage, respectively. There was no significant or minimal difference in the coefficient of friction between samples from different regions of the knee, or animals, or when the cartilage samples were frozen for 1 day or 2 days before testing. However, changing lubricant from deionized water to ionic media, for example, saline or simulated body fluid, increased the coefficient of friction significantly. PMID:26614798

  14. New holographic polymeric composition based on plexiglass, polyvinyl butyral, and phenanthrenquinone

    NASA Astrophysics Data System (ADS)

    Matusevich, Vladislav; Tolstik, Elen; Kowarschik, Richard; Egorova, Elena; Matusevich, Yuri I.; Krul, Leonid

    2013-05-01

    The newly developed Plexiglas films containing polyvinyl butyral resins and phenanthrenequinone molecules as photosensitive dopant, which are proposed for the practical application as interlayer of laminated safety glass, are shown for the first time. The injection of the phenanthrenequinone-poly(methyl methacrylate) into the polyvinyl butyral protective interlayer provides a homogenous distribution of the recording holographic medium in the layer and allows fixing the entire surface grating in the laminated glass. In addition, the original properties of polyvinyl butyral as a connecting material were preserved during manufacturing of the laminated glass. This allows a recording of holographic structures directly after baking of the laminated glass, thus reducing the destruction of the gratings due to the elevated temperatures. The diffractive structures in phenanthrenequinone-poly(methyl methacrylate)-polyvinyl butyral polymeric layers with thicknesses of hundreds of microns are sealed between two panels of glass (so-called laminated glass) and are generated by illumination with an Argon-laser of 514 nm. Efficiently fixed and long-term stable holographic gratings recorded in the phenanthrenequinone-poly(methyl methacrylate)-polyvinyl butyral layer enable to produce transparent laminated glass with inserted diffractive elements, which can be used e.g. for Head-up Displays in automobile windshields or as holographic light concentrators for solar cells.

  15. Fragrance material review on ?-methylbenzyl acetate.

    PubMed

    McGinty, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of ?-methylbenzyl acetate when used as a fragrance ingredient is presented. ?-Methylbenzyl acetate is a member of the fragrance structural group Aryl Alkyl Alcohol Simple Acid Esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for ?-methylbenzyl acetate were evaluated, then summarized, and includes: physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, elicitation, and repeated dose data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22406576

  16. Fragrance material review on benzyl acetate.

    PubMed

    McGinty, D; Vitale, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of benzyl acetate when used as a fragrance ingredient is presented. Benzyl acetate is a member of the fragrance structural group aryl alkyl alcohol simple acid esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for benzyl acetate were evaluated, then summarized, and includes: physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, elicitation, phototoxicity, toxicokinetics, repeated dose, reproductive toxicity, genotoxicity, or carcinogenicity data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Refer Belsito et al. (2012) for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22387848

  17. Process for the preparation of vinyl acetate

    DOEpatents

    Tustin, G.C.; Zoeller, J.R.; Depew, L.S.

    1998-02-17

    This invention pertains to the preparation of vinyl acetate by contacting within a contact zone a mixture of ketene and acetaldehyde with an acid catalyst at about one bar pressure and between about 85 and 200 C and removing the reaction products from the contact zone.

  18. Process for the preparation of vinyl acetate

    DOEpatents

    Tustin, Gerald Charles (Kingsport, TN); Zoeller, Joseph Robert (Kingsport, TN); Depew, Leslie Sharon (Kingsport, TN)

    1998-01-01

    This invention pertains to the preparation of vinyl acetate by contacting within a contact zone a mixture of ketene and acetaldehyde with an acid catalyst at about one bar pressure and between about 85.degree. and 200.degree. C. and removing the reaction products from the contact zone.

  19. Synthesis of Cellulose Acetate from Cotton Byproducts

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Cotton burr and cottonseed hull are relatively inexpensive cotton byproducts. In an effort to derive greater value out of these natural renewable materials, we have succeeded in converting part of them into cellulose acetate without prior chemical breakdown or physical separation of cellulose, ligni...

  20. Fragrance material review on 2-phenylpropyl acetate.

    PubMed

    McGinty, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of 2-phenylpropyl acetate when used as a fragrance ingredient is presented. 2-Phenylpropyl acetate is a member of the fragrance structural group Aryl Alkyl Alcohol Simple Acid Esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for 2-phenylpropyl acetate were evaluated, then summarized, and includes: physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, and skin sensitization data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22421639

  1. Fragrance material review on phenethyl acetate.

    PubMed

    McGinty, D; Vitale, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of phenethyl acetate when used as a fragrance ingredient is presented. Phenethyl acetate is a member of the fragrance structural group aryl alkyl alcohol simple acid esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for phenethyl acetate were evaluated, then summarized, and includes: physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, elicitation, toxicokinetics, repeated dose, genotoxicity, and carcinogenicity data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22414644

  2. Fragrance material review on piperonyl acetate.

    PubMed

    McGinty, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of piperonyl acetate when used as a fragrance ingredient is presented. Piperonyl acetate is a member of the fragrance structural group aryl alkyl alcohol simple acid esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for piperonyl acetate were evaluated, then summarized, and includes: physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, toxicokinetics, and genotoxicity data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22445840

  3. Fermentative biohydrogen production from lactate and acetate.

    PubMed

    Wu, Chao-Wei; Whang, Liang-Ming; Cheng, Hai-Hsuan; Chan, Kan-Chi

    2012-06-01

    In this study, a continuous-flow stirred tank reactor (CSTR) fed with lactate and acetate was operated to enrich hydrogen-producing bacteria. By varying the influent substrate concentrations and hydraulic retention times (HRT), the volumetric loading rate (VLR) of 55.64 kg-COD/m(3)/day seemed to be optimum for this enriched culture for fermentative hydrogen production from lactate and acetate. The results of batch experiments confirmed that the enriched culture tended to fulfill the e(-) equiv requirement for cell growth at a lower VLR condition (21.77 kg-COD/m(3)/day), while it could largely distribute the e(-) equiv for hydrogen production at a higher VLR condition. However, a maximum lactate/acetate concentration allowed for enriching this culture existed, especially at a lower HRT condition in which wash-out can be an issue for this enriched culture. Finally, the results of cloning and sequencing indicated that Clostridium tyrobutyricum was considered the major hydrogen-producing bacteria in the CSTR fed with lactate and acetate. PMID:22318084

  4. Advanced Colloids Experiment (ACE-T1)

    NASA Technical Reports Server (NTRS)

    Meyer, William V.; Sicker, Ron; Brown, Dan; Eustace, John

    2015-01-01

    Increment 45 - 46 Science Symposium presentation of Advanced Colloids Experiment (ACE-T1) to RPO. The purpose of this event is for Principal Investigators to present their science objectives, testing approach, and measurement methods to agency scientists, managers, and other investigators.

  5. Phenyl Acetate Preparation from Phenol and Acetic Acid: Reassessment of a Common Textbook Misconception.

    ERIC Educational Resources Information Center

    Hocking, M. B.

    1980-01-01

    Reassesses a common textbook misconception that "...phenols cannot be esterified directly." Results of experiments are discussed and data tables provided of an effective method for the direct preparation of phenyl acetate. (CS)

  6. Characterization of the Acetate Binding Pocket in the Methanosarcina thermophila Acetate Kinase

    PubMed Central

    Ingram-Smith, Cheryl; Gorrell, Andrea; Lawrence, Sarah H.; Iyer, Prabha; Smith, Kerry; Ferry, James G.

    2005-01-01

    Acetate kinase catalyzes the reversible magnesium-dependent synthesis of acetyl phosphate by transfer of the ATP ?-phosphoryl group to acetate. Inspection of the crystal structure of the Methanosarcina thermophila enzyme containing only ADP revealed a solvent-accessible hydrophobic pocket formed by residues Val93, Leu122, Phe179, and Pro232 in the active site cleft, which identified a potential acetate binding site. The hypothesis that this was a binding site was further supported by alignment of all acetate kinase sequences available from databases, which showed strict conservation of all four residues, and the recent crystal structure of the M. thermophila enzyme with acetate bound in this pocket. Replacement of each residue in the pocket produced variants with Km values for acetate that were 7- to 26-fold greater than that of the wild type, and perturbations of this binding pocket also altered the specificity for longer-chain carboxylic acids and acetyl phosphate. The kinetic analyses of variants combined with structural modeling indicated that the pocket has roles in binding the methyl group of acetate, influencing substrate specificity, and orienting the carboxyl group. The kinetic analyses also indicated that binding of acetyl phosphate is more dependent on interactions of the phosphate group with an unidentified residue than on interactions between the methyl group and the hydrophobic pocket. The analyses also indicated that Phe179 is essential for catalysis, possibly for domain closure. Alignments of acetate kinase, propionate kinase, and butyrate kinase sequences obtained from databases suggested that these enzymes have similar catalytic mechanisms and carboxylic acid substrate binding sites. PMID:15774882

  7. Ambipolar Behavior in All-Carbon-Nanotube Field-Effect Transistors by Poly(Vinyl Alcohol) Coating

    E-print Network

    Maruyama, Shigeo

    Ambipolar Behavior in All-Carbon-Nanotube Field-Effect Transistors by Poly(Vinyl Alcohol) Coating of CNT-FETs can be changed to ambipolar behavior by poly(vinyl alcohol) (PVA) coating4 . PVA is a considerably effective dielectric polymer because it has a relatively high dielectric constant compared

  8. Hot Pin Welding of Thin Poly(vinyl chloride) Sheet James D. Van de Ven, Arthur G. Erdman

    E-print Network

    Van de Ven, James D.

    the weld pressure and temperature predicted in these models with the actual weld quality is critical parameters with weld quality. The melting temperature of polyvinyl chloride (PVC) is not well-defined, owingHot Pin Welding of Thin Poly(vinyl chloride) Sheet James D. Van de Ven, Arthur G. Erdman Mechanical

  9. 75 FR 55552 - Polyvinyl Alcohol From Taiwan: Preliminary Determination of Sales at Less Than Fair Value and...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-13

    ... FR 59204 (October 4, 2004) (Initiation Notice). On October 22, 2004, the International Trade... imports of the subject merchandise. See Polyvinyl Alcohol From Taiwan, 69 FR 63177 (October 29, 2004). As..., the CAFC affirmed the ITC's decision. See Polyvinyl Alcohol From Taiwan; Determination, 75 FR...

  10. 21 CFR 582.5892 - a-Tocopherol acetate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5892 a-Tocopherol acetate. (a) Product. a-Tocopherol acetate. (b) Conditions of use....

  11. 21 CFR 582.5892 - a-Tocopherol acetate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5892 a -Tocopherol acetate. (a) Product. a -Tocopherol acetate. (b) Conditions...

  12. 21 CFR 582.5892 - a-Tocopherol acetate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5892 a -Tocopherol acetate. (a) Product. a -Tocopherol acetate. (b) Conditions...

  13. 21 CFR 582.5892 - a-Tocopherol acetate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Nutrients and/or Dietary Supplements 1 § 582.5892 a -Tocopherol acetate. (a) Product. a -Tocopherol acetate. (b) Conditions...

  14. Expression of acetate permease-like (apl) genes in subsurface communities of Geobacter species under fluctuating acetate concentrations

    SciTech Connect

    Elifantz, H.; N'Guessan, L.A.; Mouser, P.J.; Williams, K H.; Wilkins, M J.; Risso, C.; Holmes, D.E.; Long, P.E.; Lovley, D.R.

    2010-03-01

    The addition of acetate to uranium-contaminated aquifers in order to stimulate the growth and activity of Geobacter species that reduce uranium is a promising in situ bioremediation option. Optimizing this bioremediation strategy requires that sufficient acetate be added to promote Geobacter species growth. We hypothesized that under acetate-limiting conditions, subsurface Geobacter species would increase the expression of either putative acetate symporters genes (aplI and aplII). Acetate was added to a uranium-contaminated aquifer (Rifle, CO) in two continuous amendments separated by 5 days of groundwater flush to create changing acetate concentrations. While the expression of aplI in monitoring well D04 (high acetate) weakly correlated with the acetate concentration over time, the transcript levels for this gene were relatively constant in well D08 (low acetate). At the lowest acetate concentrations during the groundwater flush, the transcript levels of aplII were the highest. The expression of aplII decreased 2-10-fold upon acetate reintroduction. However, the overall instability of acetate concentrations throughout the experiment could not support a robust conclusion regarding the role of apl genes in response to acetate limitation under field conditions, in contrast to previous chemostat studies, suggesting that the function of a microbial community cannot be inferred based on lab experiments alone.

  15. Expression of Acetate Permease-like (apl) Genes in Subsurface Communities of Geobacter Species Under Fluctuating Acetate Concentrations

    SciTech Connect

    Elifantz, H.; N'Guessan, A. L.; Mouser, Paula; Williams, Kenneth H.; Wilkins, Michael J.; Risso, Carla; Holmes, Dawn; Long, Philip E.; Lovley, Derek R.

    2010-09-01

    The addition of acetate to uranium-contaminated aquifers in order to stimulate the growth and activity of Geobacter species that reduce uranium is a promising in situ bioremediation option. Optimizing this bioremediation strategy requires that suf?cient acetate be added to promote Geobacter species growth. We hypothesized that under acetate-limiting conditions, subsurface Geobacter species would increase the expression of either putative acetate symporters genes (aplI and aplII). Acetate was added to a uranium-contaminated aquifer (Ri?e, CO) in two continuous amendments separated by 5 days of groundwater ?ush to create changing acetate concentrations. While the expression of aplI in monitoring well D04 (high acetate) weakly correlated with the acetate concentration over time, the transcript levels for this gene were relatively constant in well D08 (low acetate). At the lowest acetate concentrations during the groundwater ?ush, the transcript levels of aplII were the highest. The expression of aplII decreased 2–10-fold upon acetate reintroduction. However, the overall instability of acetate concentrations throughout the experiment could not support a robust conclusion regarding the role of apl genes in response to acetate limitation under ?eld conditions, in contrast to previous chemostat studies, suggesting that the function of a microbial community cannot be inferred based on lab experiments alone.

  16. Structural design of ketal and acetal blocking groups in two-component chemically amplified positive DUV resists

    NASA Astrophysics Data System (ADS)

    Mertesdorf, Carlo; Muenzel, Norbert; Holzwarth, Heinz E.; Falcigno, Pasquale A.; Schacht, Hans-Thomas; Rohde, Ottmar; Schulz, Reinhard; Slater, Sydney G.; Frey, David; Nalamasu, Omkaram; Timko, Allen G.; Neenan, Thomas X.

    1995-06-01

    In the present study, protecting groups of moderate stability, such as acetals and ketals, were investigated as pendant blocking groups in polyvinyl phenols. Polymers were obtained by reacting enol ethers with the phenolic side groups to form acetal or ketal blocked phenols. Decomposition temperatures, glass transition temperatures, and molecular weights of the resulting polymers were monitored and correlated with the protecting group structure. Stability of the protecting groups can be explained by protonation occurring at either of the two oxygen sites, making two cleavage routes possible. Secondary reactions of the released protecting groups in the resist film were investigated and discussed. The structure of the protecting group was designed in order to meet basic resist properties such as resolution/linearity, DOF, post exposure delay latitude and thermal stability. A Canon FPA 4500 (NA equals 0.37) and a GCA XLS exposure tool (NA equals 0.53) were used for the optimization process. A preoptimized resist formulation based on the above criteria exhibits 0.23 micrometers line/space resolution, 0.8 micrometers focus latitude at 0.25 micrometers resolution and approximately two hours post exposure delay latitude.

  17. Structural and electronic properties of poly(vinyl alcohol) using density functional theory

    SciTech Connect

    Dabhi, Shweta Jha, Prafulla K.

    2014-04-24

    The first principles calculations have been carried out to investigate the structural, electronic band structure density of states along with the projected density of states for poly(vinyl alcohol). Our structural calculation suggests that the poly(vinyl alcohol) exhibits monoclinic structure. The calculated structural lattice parameters are in excellent agreement with available experimental values. The band structure calculations reveal that the direct and indirect band gaps are 5.55 eV and 5.363 eV respectively in accordance with experimental values.

  18. Viscometric study of chitosan solutions in acetic acid/sodium acetate and acetic acid/sodium chloride.

    PubMed

    Costa, Cristiane N; Teixeira, Viviane G; Delpech, Marcia C; Souza, Josefa Virginia S; Costa, Marcos A S

    2015-11-20

    A viscometric study was carried out at 25°C to assess the physical-chemical behavior in solution and the mean viscometric molar mass (M¯v) of chitosan solutions with different deacetylation degrees, in two solvent mixtures: medium 1-acetic acid 0.3mol/L and sodium acetate 0.2mol/L; and medium 2-acetic acid 0.1mol/L and sodium chloride 0.2mol/L. Different equations were employed, by graphical extrapolation, to calculate the intrinsic viscosities [?] and the viscometric constants, to reveal the solvent's quality: Huggins (H), Kraemer (K) and Schulz-Blaschke (SB). For single-point determination, the equations used were SB, Solomon-Ciuta (SC) and Deb-Chanterjee (DC), resulting in a faster form of analysis. The values of ?M¯v were calculated by applying the equation of Mark-Houwink-Sakurada. The SB and SC equations were most suitable for single-point determination of [?] and ?M¯v and the Schulz-Blachke constant (kSB), equal to 0.28, already utilized for various systems, can also be employed to analyze chitosan solutions under the conditions studied. PMID:26344278

  19. 21 CFR 522.2478 - Trenbolone acetate and estradiol benzoate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Trenbolone acetate and estradiol benzoate. 522... ANIMAL DRUGS § 522.2478 Trenbolone acetate and estradiol benzoate. (a) Specifications. Each implant dose... estradiol benzoate. (2) 4 pellets, each pellet containing 25 mg trenbolone acetate and 3.5 mg...

  20. Kinetics of Ethyl Acetate Synthesis Catalyzed by Acidic Resins

    ERIC Educational Resources Information Center

    Antunes, Bruno M.; Cardoso, Simao P.; Silva, Carlos M.; Portugal, Ines

    2011-01-01

    A low-cost experiment to carry out the second-order reversible reaction of acetic acid esterification with ethanol to produce ethyl acetate is presented to illustrate concepts of kinetics and reactor modeling. The reaction is performed in a batch reactor, and the acetic acid concentration is measured by acid-base titration versus time. The…

  1. Acetate concentrations and oxidation in salt marsh sediments

    NASA Technical Reports Server (NTRS)

    1992-01-01

    Acetate concentrations and rates of acetate oxidation and sulfate reduction were measured in S. alterniflora sediments in New Hampshire and Massachusetts. Pore water extracted from cores by squeezing or centrifugation contained in greater than 0.1 mM acetate and, in some instances, greater than 1.0 mM. Pore water sampled nondestructively contained much less acetate, often less than 0.01 mM. Acetate was associated with roots, and concentrations varied with changes in plant physiology. Acetate turnover was very low whether whole core or slurry incubations were used. Radiotracers injected directly into soils yielded rates of sulfate reduction and acetate oxidation not significantly different from core incubation techniques. Regardless of incubation method, acetate oxidation did not account for a substantial percentage of sulfate reduction. These results differ markedly from data for unvegetated coastal sediments where acetate levels are low, oxidation rate constants are high, and acetate oxication rates greatly exceed rates of sulfate reduction. The discrepancy between rates of acetate oxidation and sulfate reduction in these marsh soils may be due either to the utilization of substrates other than acetate by sulfate reducers or artifacts associated with measurements of organic utilization by rhizosphere bacteria. Care must be taken when interpreting data from salt marsh sediments since the release of material from roots during coring may affect the concentrations of certain compounds as well as influencing results obtained when sediment incubations are employed.

  2. 21 CFR 522.2477 - Trenbolone acetate and estradiol.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...trenbolone acetate and 24 mg estradiol (one implant consisting of 6 pellets, each pellet...trenbolone acetate and 4 mg estradiol) per implant dose. (B) 120 mg trenbolone acetate and 24 mg estradiol (one implant consisting of 7 pellets, each of...

  3. 21 CFR 582.5933 - Vitamin A acetate.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Vitamin A acetate. 582.5933 Section 582.5933 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Supplements 1 § 582.5933 Vitamin A acetate. (a) Product. Vitamin A acetate. (b) Conditions of use....

  4. 21 CFR 582.5933 - Vitamin A acetate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Vitamin A acetate. 582.5933 Section 582.5933 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Supplements 1 § 582.5933 Vitamin A acetate. (a) Product. Vitamin A acetate. (b) Conditions of use....

  5. 21 CFR 582.5933 - Vitamin A acetate.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Vitamin A acetate. 582.5933 Section 582.5933 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Supplements 1 § 582.5933 Vitamin A acetate. (a) Product. Vitamin A acetate. (b) Conditions of use....

  6. 21 CFR 582.5933 - Vitamin A acetate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Vitamin A acetate. 582.5933 Section 582.5933 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Supplements 1 § 582.5933 Vitamin A acetate. (a) Product. Vitamin A acetate. (b) Conditions of use....

  7. 21 CFR 582.5933 - Vitamin A acetate.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Vitamin A acetate. 582.5933 Section 582.5933 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Supplements 1 § 582.5933 Vitamin A acetate. (a) Product. Vitamin A acetate. (b) Conditions of use....

  8. Perylenetetracarboxylic diimide (PTCDI) nanowires for sensing ethyl acetate in wine.

    PubMed

    Khopkar, Yashdeep; Kojtari, Arben; Swearer, Dayne; Zivanovic, Sandra; Ji, Hai-Feng

    2014-09-01

    We report the application of perylenetetracarboxylic diimide (PTCDI) nanowires for sensing ethyl acetate. The conductivity of the crystalline nano/microwires increases quickly and selectively in the presence of ethyl acetate vapor, but not with water, acid and alcohol vapors, suggesting that the nanowires of PTCDI may be used for monitoring ethyl acetate during a wine manufacturing process. PMID:25924331

  9. 21 CFR 584.200 - Ethyl alcohol containing ethyl acetate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... Ethyl alcohol containing ethyl acetate. The feed additive ethyl alcohol containing ethyl acetate meets the requirement of 27 CFR 21.62, being not less than 92.5 percent ethyl alcohol, each 100 gallons... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Ethyl alcohol containing ethyl acetate....

  10. 21 CFR 522.2478 - Trenbolone acetate and estradiol benzoate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Trenbolone acetate and estradiol benzoate. 522... ANIMAL DRUGS § 522.2478 Trenbolone acetate and estradiol benzoate. (a) Specifications. Each implant dose consists of: (1) 8 pellets, each pellet containing 25 milligrams (mg) trenbolone acetate and 3.5...

  11. Isothermal decomposition of ?-irradiated erbium acetate

    NASA Astrophysics Data System (ADS)

    Mahfouz, R. M.; Al-Shehri, S. M.; Monshi, M. A. S.; Alhaizan, A. I.; El-Salam, N. M. Abd

    Isothermal decomposition of un-irradiated and pre-?-irradiated erbium acetate has been investigated at different temperatures between 583 and 603 K. Irradiation was observed to enhance the rate of decomposition without modifying the mechanism of the thermal decomposition. Thermal decomposition of erbium acetate has been shown to proceed by a nucleation and growth mechanism (Erofe'ev model) both for un-irradiated and pre-?-irradiated samples. The enhancement of the decomposition was found to increase with an increase in the ?-ray dose applied to the sample and may be attributed to an increase in point defects and formation of additional nucleation centers generated in the host lattice. Thermodynamic values of the main decomposition process were calculated and evaluated.

  12. Isothermal decomposition of ?-irradiated samarium acetate

    NASA Astrophysics Data System (ADS)

    Mahfouz, R. M.; Monshi, M. A. S.; Alshehri, S. M.; Abd El-Salam, N. M.

    2000-10-01

    Isothermal decomposition of un-irradiated and pre-?-irradiated samarium acetate has been investigated at different temperatures between 613 and 633 K. Irradiation was observed to enhance the rate of decomposition without modifying the mechanism of thermal decomposition. Thermal decomposition of samarium acetate has been shown to proceed by two-dimensional phase-boundary reaction both for un-irradiated and pre-?-irradiated samples. The enhancement of the decomposition was found to increase with an increase in the ?-ray dose applied to the sample and may be attributed to an increase in point defects and formation of additional nucleation centers generated in the host lattice. Thermodynamic values of the main decomposition process were calculated and evaluated.

  13. Multiple-anion nonvolatile acetal (MANA) resists

    NASA Astrophysics Data System (ADS)

    Guevremont, Jeffrey M.; Brainard, Robert L.; Reeves, Scott D.; Zhou, Xin; Nguyen, Thinh B.; Mackevich, Joseph F.; Anderson, Erik H.; Taylor, Gary N.

    2001-08-01

    New acetal or ketal blocking reagents were investigated for use in e-beam lithography and compared with the performance of ethyl vinyl either (EVE). Three blocking groups, (alpha) -Angelicalactone (AL), 6-methylene-5,6-benzo-1,4- dioxane (MBD), and MANA50 (an undisclosed blocking group used to show the potential of this chemistry) were reacted with poly(p-hydroxystyrene) (PHS) under acid catalyzed conditions to form AL-PHS, MBD-PHS, MANA50-PHS. The performance objectives pursued in the design of these new materials was to use acetal (ketal) chemistry to deliver wide process latitudes (e.g. good PED performance and minimal PEB sensitivity), use high molecular weight blocking groups to eliminate outgassing, and use the novel concept of multiple anions to deliver lithographic performance. These new materials are called Multiple Anion Nonvolatile Acetal (MANA) resists. Resists films were exposed with 50kV electrons, post exposure baked (PEB), and developed with 0.26 N TMAH. Resists prepared with the third blocking group, MANA50, gave contrast and imaging performance independent of PEB humidity and were relatively insensitive to PEB temperature and post exposure delay (PED). These resists gave the best resolution (90 nm) and profiles of all the materials tested, as well as showing no outgassing (as measured by film thickness loss).

  14. Bicarbonate versus acetate hemodialysis in ventilated patients.

    PubMed

    van Geelen, J A; Woittiez, A J; Schalekamp, M A

    1987-09-01

    Hemodynamic tolerance to bicarbonate versus acetate hemodialysis was studied in seven ventilated, critically ill patients, suffering from acute renal failure. Both kinds of hemodialysis were carried out with a recirculating dialysate delivery system and a relatively low blood flow (180 ml/min). Each patient underwent two hemodialysis procedures, one with bicarbonate and one with acetate, lasting for four hours. Ultrafiltration rates were kept below 250 ml/h and only biocompatible membranes with a relatively small surface area (Biospal 2400, Hospal, France) were used. Despite the mild hemodialysis conditions, hypotensive episodes with a mean blood pressure below 70 mmHg were observed in 3 out of 7 bicarbonate sessions and 4 out of 7 acetate sessions. Thus, we could not demonstrate a hemodynamic advantage of bicarbonate hemodialysis in this group of ventilated patients. This contrasts with other studies conducted in non-ventilated patients. Prevention of hypoxemia by mechanical ventilation and control of vascular tone by the use of vasoactive drugs may be of more clinical relevance than the kind of hemodialysis procedure that is used. PMID:3117466

  15. Organic/inorganic nanocomposites, methods of making, and uses as a permeable reactive barrier

    DOEpatents

    Harrup, Mason K. (Idaho Falls, ID); Stewart, Frederick F. (Idaho Falls, ID)

    2007-05-15

    Nanocomposite materials having a composition including an inorganic constituent, a preformed organic polymer constituent, and a metal ion sequestration constituent are disclosed. The nanocomposites are characterized by being single phase, substantially homogeneous materials wherein the preformed polymer constituent and the inorganic constituent form an interpenetrating network with each other. The inorganic constituent may be an inorganic oxide, such as silicon dioxide, formed by the in situ catalyzed condensation of an inorganic precursor in the presence of the solvated polymer and metal ion sequestration constituent. The polymer constituent may be any hydrophilic polymer capable of forming a type I nanocomposite such as, polyacrylonitrile (PAN), polyethyleneoxide (PEO), polyethylene glycol (PEG), polyvinyl acetate (PVAc), polyvinyl alcohol (PVA), and combinations thereof. Nanocomposite materials of the present invention may be used as permeable reactive barriers (PRBs) to remediate contaminated groundwater. Methods for making nanocomposite materials, PRB systems, and methods of treating groundwater are also disclosed.

  16. Novel, Facile, Single-Step Technique of Polymer/TiO? Nanofiber Composites Membrane for Photodegradation of Methylene Blue.

    PubMed

    Abdal-hay, Abdalla; Makhlouf, Abdel Salam Hamdy; Khalil, Khalil Abdelrazek

    2015-06-24

    Novel photocatalyst membrane materials were successfully fabricated by an air jet spinning (AJS) technique from polyvinyl acetate (PVAc) solutions containing nanoparticles (NPs) of titanium dioxide (TiO2). Our innovative strategy for the production of composite nanofibers is based on stretching a solution of polymer with a high-speed compressed air jet. This enabled us to rapidly cover different substrates with TiO2/PVAc interconnected nanofibers. Surprisingly, the diameters of the as-spun fibers were found to decrease with increasing amount of NPs. Our results showed that AJS PVAc-based fibrous membranes with average fiber diameters of 505-901 nm have an apparent porosity of about 79-93% and a mean pore size of 1.58-5.12 ?m. Embedding NPs onto the as-spun fibers resulted in increasing the tensile strength of the obtained composite fiber mats. The photodegradation property of TiO2 membrane mats proved a high efficiency in the decomposition of methylene blue dye. The novel fiber spinning technique discussed in this paper can provide the capacity to lace together a variety of types of polymers, fibers and particles to produce interconnected fibers layer. Our approach, therefore, opens the door for the innovation in nanocomposite mat that has great potential as efficient and economic water filter media and as reusable photocatalyst. PMID:25985264

  17. CORROSION OF LEAD SHIELDING IN MODEL 9975 PACKAGE

    SciTech Connect

    Subramanian, K

    2006-03-15

    Experiments were performed to determine the corrosion rate of lead when exposed to off-gas or degradation products of organic materials used in the model 9975 package.[1] The experiments were completed within the framework of a parametric test matrix with variables of organic configuration, temperature, humidity and the effect of durations of exposure on the corrosion of lead in the 9975 package. The room temperature vulcanizing (RTV) sealant was the most corrosive organic species in the testing, followed by the polyvinyl acetate (PVAc) glue. The Celotex{copyright} material uniquely induced measurable corrosion only in situations with condensed water, and to a much lesser extent than the PVAc glue and RTV. The coupons exhibited faster corrosion at higher temperatures than at room temperatures. There was a particularly pronounced effect of condensed water as the coupons exposed in the cells with condensed water exhibited much higher corrosion rates. In the 9975 package, the PVAc glue was determined to be the most aggressive due to it's proximity in the design. The condition considered most representative of the package conditions is that of the coupon exposed to the Celotex{copyright}/glue organic exposed in the ambient humidity conditions. The corrosion rate of 2 mpy measured in the laboratory experiments for this condition is considered to be a bounding condition to the 9975 package conditions when the laboratory results are extrapolated to actual package conditions, and is recommended as a conservative estimate for package performance calculations.

  18. Vibrational, ac impedance and dielectric spectroscopic studies of poly(vinylacetate)- N, N-dimethylformamide-LiClO 4 polymer gel electrolytes

    NASA Astrophysics Data System (ADS)

    Baskaran, R.; Selvasekarapandian, S.; Hirankumar, G.; Bhuvaneswari, M. S.

    Polymer electrolyte membranes that consist of poly(vinyl acetate) (PVAc) and LiClO 4 with different concentrations of plasticizer ( N, N-dimethylformamide (DME) have been prepared by a solution-casting technique. The formation of polymer-salt complexes has been confirmed by FT-IR spectral studies. Conductivity studies have been carried out using ac impedance spectroscopy in the frequency range 42 Hz-5 MHz. The influence of the addition of plasticizer (DMF) on the ionic conductivity of the PVAc-LiClO 4 polymer electrolyte complex has been discussed. The maximum value of bulk conductivity for PVAc(70)-DMF(20)-LiClO 4(10) system is found to be 4.2×10 -4 S cm -1 at 303 K. The temperature dependence of the conductivity of the polymer electrolytes follows the Vogel-Tamman-Fulcher relationship. Transport properties, such as activation energy and charge carrier concentration, have been calculated from the VTF formalism. The ionic transference number of the mobile ions has been estimated by Wagner's polarization method and is found to be ?0.96 for all the samples.

  19. A Self-Assembled, Low-Cost, Microstructured Layer for Extremely Stretchable Gold Films.

    PubMed

    Filiatrault, Heather L; Carmichael, R Stephen; Boutette, Rachel A; Carmichael, Tricia Breen

    2015-09-23

    We demonstrate a simple, low-cost, and green approach to deposit a microstructured coating on the silicone elastomer polydimethylsiloxane (PDMS) that can be coated with gold to produce highly stretchable and conductive films. The microstructured coating is fabricated using an aqueous emulsion of poly(vinyl acetate) (PVAc): common, commercially available white glue. The aqueous glue emulsion self-assembles on the PDMS surface to generate clustered PVAc globules, which can be conformally coated with gold. The microstructured surface provides numerous defect sites that localize strain when the structure is stretched, resulting in the initiation of numerous microcracks. As the structure is further elongated, the microcracks interact with one another, preventing long-range crack propagation and thus preserving the conduction pathway. The resistance of PDMS/glue/gold structures remains remarkably low (23 times the initial resistance) up to 65% elongation, making these structure useful as stretchable interconnects. Decreasing the concentration of the PVAc aqueous emulsion reduces the density of defect sites of the microstructure, which increases the change in resistance of the gold films with stretching. In this way, we can tune the resistance changes of the PDMS/glue/gold structures and increase their sensitivity to strain. We demonstrate the use of these structures as wearable, soft strain sensors. PMID:26302030

  20. Near-Infrared Laser Absorption of Poly(vinyl chloride) at Elevated Temperatures

    E-print Network

    Van de Ven, James D.

    , unpigmented state are highly transmissive of light in the near-infrared range, thus allowing laser of light detection [2, 3]. Within the near-infrared region nat- ural polymers have nearly no absorption [2Near-Infrared Laser Absorption of Poly(vinyl chloride) at Elevated Temperatures James D. Van de Ven

  1. Mechanistic analysis of protein delivery from porous poly(vinyl alcohol) systems

    E-print Network

    Peppas, Nicholas A.

    and swell when immersed in water. The extent of the swelling is determined by the density of cross285 Mechanistic analysis of protein delivery from porous poly(vinyl alcohol) systems N.A. Peppas(vinyl alcohol) (PVA) hydrogels that can be used as carriers to release proteins. Non-porous gels were prepared

  2. FOAMED ARTICLES BASED ON POTATO STARCH, CORN AND WHEAT FIBRE, AND POLY(VINYL ALCOHOL)

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Continued research cooperation between USDA Laboratories (USA) and the University of Pisa, Italy, has yielded several composites based on blends of poly(vinyl alcohol) (PVA) and either corn or wheat fibres, co-product of the corn-wheat wet-milling process. Foam trays were prepared by baking the blen...

  3. Hybrid composite based on poly(vinyl alcohol) and fillers from renewable resources

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Hybrid composite laminates consisting of polyvinyl alcohol (PVA) as continuous phase and lignocellulosic fibres, derived from sugarcane bagasse, apple and orange waste were moulded in a carver press in the presence of water and glycerol such as platicizers agents. Corn starch was introduced as a bio...

  4. Simultaneous measurement of laser reflection and transmission of poly,,vinyl chloride...

    E-print Network

    Van de Ven, James D.

    Simultaneous measurement of laser reflection and transmission of poly,,vinyl chloride... James D rigid poly vinyl chloride from a diode laser source. Total reflection is quantified by numerically of clear rigid poly vinyl chloride was calculated. In addition the quantity and distribution of light

  5. Short communication Poly(vinyl alcohol) separators improve the coulombic efficiency of

    E-print Network

    cathodes are lower in cost than previous designs by avoiding the use of expensive porous carbon cloth carbon cathodes in microbial fuel cells Guang Chen a,b , Fang Zhang b , Bruce E. Logan b, , Michael A Keywords: Microbial fuel cell Activated carbon Separator Cathode Poly(vinyl alcohol) High

  6. Polyvinyl chloride film local isometric heat treatment for hidden 3D printing on polymer packaging

    E-print Network

    Volinsky, Alex A.

    Polyvinyl chloride film local isometric heat treatment for hidden 3D printing on polymer packaging with poor vision, but capable of tactile marking recognition and reading Braille. This 3D printing is based of 3D printing, including tactile sign formation conditions. VC 2015 Wiley Periodicals, Inc. J. Appl

  7. Modeling of crystal dissolution of poly(vinyl alcohol) gels produced by freezing/thawing processes

    E-print Network

    Peppas, Nicholas A.

    Modeling of crystal dissolution of poly(vinyl alcohol) gels produced by freezing/thawing processes C.M. Hassan1 , J.H. Ward, N.A. Peppas* Polymer Science and Engineering Laboratories, School. The dissolution process was described as a three-step mechanism: detachment-, diffusion-, and disentanglement

  8. CHARACTERIZATION OF BIODEGRADABLE COMPOSITE FILMS PREPARED FROM BLENDS OF POLYVINYL ALCOHOL, CORNSTARCH AND LIGNOCELLULOSICC FIBER

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Several composite blends of poly(vinyl alcohol) (PVA) and lignocellulosic fibers were prepared and characterized. Cohesive and flexible cast films were obtained by blending lignocellulosic fibers derived from orange waste and PVA with or without cornstarch. Films were evaluated for their thermal s...

  9. Linear Dichroism of Cyanine Dyes in Stretched Polyvinyl Alcohol Films: A Physical Chemistry Laboratory Experiment.

    ERIC Educational Resources Information Center

    Natarajan, L. V.; And Others

    1983-01-01

    Provides background information, procedures, and results of an undergraduate physical chemistry experiment on the polarization of absorption spectra of cyanine dyes in stretched polyvinyl alcohol films. The experiment gives a simple demonstration of the concept of linear dichromism and the validity of the TEM method used in the analyses. (JN)

  10. A polyvinyl alcohol-coated silica gel stationary phase for hydrophilic interaction chromatography.

    PubMed

    Ji, Shunli; Zheng, Yang; Zhang, Feifang; Liang, Xinmiao; Yang, Bingcheng

    2015-09-21

    Multiple layers of polyvinyl alcohol (PVA) coating are generated onto silica gel by thermal immobilization to form a stationary phase applied for hydrophilic interaction liquid chromatography (HILIC). It offers an easy way to manipulate the thickness of PVA coating and the obtained stationary phase demonstrated high efficiency and high chemical stability. PMID:26280030

  11. Hybrid composite based on poly(vinyl alcohol) and fillers from renewable resources

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Hybrid composite laminates consisting of polyvinyl alcohol (PVA) as continuous phase (33% by weight) and lignocellulosic fillers, derived from sugarcane bagasse, apple and orange waste (22% by weight) were molded in a carver press in the presence of water and glycerol such as platicizers agents. Cor...

  12. 78 FR 39256 - Polyvinyl Alcohol From Taiwan: Rescission of Antidumping Duty Administrative Review; 2012-2013

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-07-01

    ... FR 13858 (March 1, 2013). \\2\\ See Initiation of Antidumping and Countervailing Duty Administrative Reviews and Request for Revocation in Part, 78 FR 25418 (May 1, 2013). On May 24, 2013, CCPC withdrew its... International Trade Administration Polyvinyl Alcohol From Taiwan: Rescission of Antidumping Duty...

  13. Comparison of storage stability of odorous VOCs in polyester aluminum and polyvinyl fluoride tedlar bags

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Whole air sampling using containers such as flexible bags or rigid canisters is commonly used to collect samples of volatile organic compounds (VOC) in air. The objective of this study was to compare the stability of polyester aluminum (PEA) and polyvinyl fluoride (PVF, brand name Tedlar®) bags for ...

  14. The Rheological Properties of Poly(Vinyl Alcohol) Gels from Rotational Viscometry

    ERIC Educational Resources Information Center

    Hurst, Glenn A.; Bella, Malika; Salzmann, Christoph G.

    2015-01-01

    A laboratory experiment was developed to follow the gelation of a polyvinyl alcohol (PVA) solution upon addition of borax by using rotational viscometry. The rheological properties of the gel were examined, measuring the dependence of viscosity and shear stress on the shear rate. Time-dependent studies were also conducted in which the viscosity of…

  15. Oxidative mineralization and characterization of polyvinyl alcohol for compatibility with tank farm processing chemistry

    SciTech Connect

    Oji, L.N.

    2000-01-04

    Polyvinyl alcohol (PVA) material has been evaluated for use as a cost-effective substitute for conventional cellulose-based disposal materials (decontamination mops and wipes), plastic bags, and disposable personal protection clothing, that are currently used at Savannah River Site. This study also provides process design criteria for ultraviolet/ultrasonic/hydrogen peroxide PVA reactor system.

  16. Electrospun nanofibers of poly(vinyl alcohol)reinforced with cellulose nanofibrils

    Technology Transfer Automated Retrieval System (TEKTRAN)

    In this work, nanofibers of poly(vinyl alcohol) (PVA) reinforced with cellulose nanofibrils (CnF) were produced by electrospinning. The effects of applied voltage, polymer concentration and injection rate, tip-to-collector distance (TCD), rotation speed of the collector, and relative humidity on mor...

  17. Antimicrobial Effect of An Essential Oil Blend on Surface-attached Salmonella on Polyvinyl Chloride

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Polyvinyl chloride (PVC) is basic material for drinking water lines for chickens. Inner surface of PVC pipe can be susceptible to surface-attachment of Salmonella, the 1st stage of biofilm development. Biofilm which can cause Salmonella infection to chickens are known to have great resistance agains...

  18. Recovery of agricultural odors and odorous compounds from polyvinyl fluoride film bags

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Accurate sampling methods are necessary when quantifying odor and volatile organic compound emissions at agricultural facilities. The commonly accepted methodology in the U.S. has been to collect odor samples in polyvinyl fluoride bags (PVF, brand name Tedlar®) and, subsequently, analyze with human ...

  19. Neutron attenuation characteristics of polyethylene, polyvinyl chloride, and heavy aggregate concrete and mortars

    SciTech Connect

    Abdul-Majid, S.; Othman, F.

    1994-03-01

    Polyethylene and polyvinyl chloride pellets were introduced into concrete to improve its neutron attenuation characteristics while several types of heavy coarse aggregates were used to improve its gamma ray attenuation properties. Neutron and gamma ray attenuation were studied in concrete samples containing coarse aggregates of barite, pyrite, basalt, hematite, and marble as well as polyethylene and polyvinyl chloride pellets in narrow-beam geometry. The highest neutron attenuation was shown by polyethylene mortar, followed by polyvinyl chloride mortar; barite and pyrite concrete showed higher gamma ray attenuation than ordinary concrete. Broad-beam and continuous (infinite) medium geometries were used to study the neutron attenuation of samples containing polymers at different concentrations with and without heavy aggregates, the fitting equations were established, and from these the neutron removal coefficients were deduced. In a radiation field of neutrons and gamma rays, the appropriate concentration of polymer and heavy aggregate can be selected to give the optimum total dose attenuation depending on the relative intensities of each type of radiation. This would give much better design flexibility over ordinary concrete. The compressive strength tests performed on mortar and concrete samples showed that their value, in general, decreases as polymer concentration increases and that the polyvinyl chloride mortar showed higher values than the polyethylene mortar. For general construction purposes, the compression strength was considered acceptable in these samples. 34 refs., 16 figs., 4 tabs.

  20. 75 FR 38079 - Postponement of Preliminary Determination of Antidumping Duty Investigation: Polyvinyl Alcohol...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-07-01

    ...-Dumping Duty Investigation: Polyvinyl Alcohol From Taiwan, 69 FR 59204 (October 4, 2004). On October 22... injury due to imports of the subject merchandise. The CIT affirmed the ITC's remand determination. DuPont... From Taiwan; Determination, 75 FR 15726 (March 30, 2010). The ITC notified the Department of...

  1. Films from spruce galactoglucomannan blended with poly(vinyl alcohol), corn arabinoxylan and konjac glucomannan

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The improvement of mechanical properties of spruce galactoglucomannan (GGM)-based films was sought by blending GGM with each of poly(vinyl alcohol) (PVOH), corn arabinoxylan (cAX), and konjac glucomannan (KGM). The blend ratios were 3:1, 1:1, and 1:3(w/w), and in addition films were made from each o...

  2. Can Palladium Acetate Lose Its "Saltiness"? Catalytic Activities of the Impurities in Palladium Acetate.

    PubMed

    Carole, William A; Bradley, Jonathan; Sarwar, Misbah; Colacot, Thomas J

    2015-11-01

    Commercially available palladium acetate often contains two major impurities, whose presence can impact the overall catalytic efficacy. This systematic study provides a comparison of the differences in catalytic activity of pure palladium acetate, Pd3(OAc)6, with the two impurities: Pd3(OAc)5(NO2) and polymeric [Pd(OAc)2]n in a variety of cross-coupling reactions. The solid state (13)C NMR spectra of all three compounds in conjunction with DFT calculations confirm their reported geometries. PMID:26507318

  3. Analysis of plasticizers in poly(vinyl chloride) medical devices for infusion and artificial nutrition: comparison and optimization of the extraction procedures, a pre-migration test step.

    PubMed

    Bernard, Lise; Cueff, Régis; Bourdeaux, Daniel; Breysse, Colette; Sautou, Valérie

    2015-02-01

    Medical devices (MDs) for infusion and enteral and parenteral nutrition are essentially made of plasticized polyvinyl chloride (PVC). The first step in assessing patient exposure to these plasticizers, as well as ensuring that the MDs are free from di(2-ethylhexyl) phthalate (DEHP), consists of identifying and quantifying the plasticizers present and, consequently, determining which ones are likely to migrate into the patient's body. We compared three different extraction methods using 0.1 g of plasticized PVC: Soxhlet extraction in diethyl ether and ethyl acetate, polymer dissolution, and room temperature extraction in different solvents. It was found that simple room temperature chloroform extraction under optimized conditions (30 min, 50 mL) gave the best separation of plasticizers from the PVC matrix, with extraction yields ranging from 92 to 100% for all plasticizers. This result was confirmed by supplemented Fourier transform infrared spectroscopy-attenuated total reflection (FTIR-ATR) and gravimetric analyses. The technique was used on eight marketed medical devices and showed that they contained different amounts of plasticizers, ranging from 25 to 36% of the PVC weight. These yields, associated with the individual physicochemical properties of each plasticizer, highlight the need for further migration studies. PMID:25577357

  4. An evaluation of the biocompatibility properties of a salt-modified polyvinyl alcohol hydrogel for a knee meniscus application.

    PubMed

    Hayes, Jennifer C; Kennedy, James E

    2016-02-01

    The treatment of irreparable knee meniscus tears remains a major challenge for the orthopaedic community. The main purpose of this research was to analyse the biocompatibility properties of a salt-modified polyvinyl alcohol hydrogel, in order to assess its potential for use as an artificial meniscal implant. Aqueous polyvinyl alcohol was treated with a sodium sulphate solution to precipitate out the polyvinyl alcohol resulting in a pliable hydrogel. Cytotoxicological analysis indicates that PVA/sodium sulphate hydrogels display a non-toxic disposition and were found to be compatible with the L929 fibroblast cell line. PMID:26652445

  5. Electron tunneling studies of Mn12-Acetate 

    E-print Network

    Ma, Lianxi

    2008-10-10

    dependence. In the region |V |?0.04 V, we find a zero-bias feature (ZBF) in which the differential conductance is suppressed. In some samples, we observe I?V staircases which we attribute to electrons “hopping” between the electrodes and the molecules.... The observed hystere- sis was attributed to the slow relaxation of molecules re-orienting within the junction. Abrupt conductance jumps at a bias voltage of -0.12 V were also observed and may indicate state transitions in the Mn 12 -Acetate molecules...

  6. Crystal growth of calcium carbonate on the cellulose acetate/pyrrolidon blend films in the presence of L-aspartic acid

    NASA Astrophysics Data System (ADS)

    Zhang, Xiuzhen; Xie, Anjian; Huang, Fangzhi; Shen, Yuhua

    2014-03-01

    The morphogenesis and growth process of calcium carbonate on the cellulose acetate/polyvinyl pyrrolidone (CA/PVP) blend films in the presence of L-aspartic acid was carefully investigated. The results showed that the concentration of L-aspartic acid, the initial pH value of reaction solution and temperature turned out to be important factors for the control of morphologies and polymorphs of calcium carbonate. Complex morphologies of CaCO3 particles, such as cubes, rose-like spheres, twinborn-spheres, cone-like, bouquet-like, etc. could be obtained under the different experimental conditions. The dynamic process of formation of rose-like sphere crystals was analyzed by monitoring the continuous morphological and structural evolution and components of crystals in different crystal stages. This research may provide a promising method to prepare other inorganic materials with complex morphologies.

  7. Phytogenic biosynthesis and emission of methyl acetate.

    PubMed

    Jardine, Kolby; Wegener, Frederik; Abrell, Leif; van Haren, Joost; Werner, Christiane

    2014-02-01

    Acetylation of plant metabolites fundamentally changes their volatility, solubility and activity as semiochemicals. Here we present a new technique termed dynamic (13) C-pulse chasing to track the fate of C1-3 carbon atoms of pyruvate into the biosynthesis and emission of methyl acetate (MA) and CO2 . (13) C-labelling of MA and CO2 branch emissions respond within minutes to changes in (13) C-positionally labelled pyruvate solutions fed through the transpiration stream. Strong (13) C-labelling of MA emissions occurred only under pyruvate-2-(13) C and pyruvate-2,3-(13) C feeding, but not pyruvate-1-(13) C feeding. In contrast, strong (13) CO2 emissions were only observed under pyruvate-1-(13) C feeding. These results demonstrate that MA (and other volatile and non-volatile metabolites) derive from the C2,3 atoms of pyruvate while the C1 atom undergoes decarboxylation. The latter is a non-mitochondrial source of CO2 in the light generally not considered in studies of CO2 sources and sinks. Within a tropical rainforest mesocosm, we also observed atmospheric concentrations of MA up to 0.6 ppbv that tracked light and temperature conditions. Moreover, signals partially attributed to MA were observed in ambient air within and above a tropical rainforest in the Amazon. Our study highlights the potential importance of acetyl coenzyme A (CoA) biosynthesis as a source of acetate esters and CO2 to the atmosphere. PMID:23862653

  8. Immunotoxicity of trenbolone acetate in Japanese quail

    USGS Publications Warehouse

    Quinn, M.J.; McKernan, M.; Lavoie, E.T.; Ottinger, M.A.

    2007-01-01

    Trenbolone acetate is a synthetic androgen that is currently used as a growth promoter in many meat-exporting countries. Despite industry laboratories classifying trenbolone as nonteratogenic, data showed that embryonic exposure to this androgenic chemical altered development of the immune system in Japanese quail. Trenbolone is lipophilic, persistent, and released into the environment in manure used as soil fertilizer. This is the first study to date to assess this chemical's immunotoxic effects in an avian species. A one-time injection of trenbolone into yolks was administered to mimic maternal deposition, and subsequent effects on the development and function of the immune system were determined in chicks and adults. Development of the bursa of Fabricius, an organ responsible for development of the humoral arm of the immune system, was disrupted, as indicated by lower masse, and smaller and fewer follicles at day 1 of hatch. Morphological differences in the bursas persisted in adults, although no differences in either two measures of immune function were observed. Total numbers of circulating leukocytes were reduced and heterophil-lymphocyte ratios were elevated in chicks but not adults. This study shows that trenbolone acetate is teratogenic and immunotoxic in Japanese quail, and provides evidence that the quail immune system may be fairly resilient to embryonic endocrine-disrupting chemical-induced alterations following no further exposure posthatch.

  9. Quantitative analysis of heavy metals emission during the combustion and baling of polyvinyl chloride insulated copper wire 

    E-print Network

    Pickard, David Paul

    1996-01-01

    The purpose of this research was the identification of heavy metals and other potentially harmful elements emitted during the combustion and baling of polyvinyl chloride insulated copper wire. Analysis of the smoke produced during the burning...

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

    E-print Network

    Sanglimsuwan, Apiradee

    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 ...

  11. Thermal decomposition of acetate: III. Catalysis by mineral surfaces

    NASA Astrophysics Data System (ADS)

    Bell, Julie L. S.; Palmer, Donald A.; Barnes, H. L.; Drummond, S. E.

    1994-10-01

    The kinetics of thermal decarboxylation of aqueous solutions of acetic acid and sodium acetate were evaluated at 335 and 355°C in contact with various surfaces as potential catalysts. Quartz, fused quartz, calcite, natural pyrite, titanium oxide, and Au apparently do not catalyze aqueous decarboxylation reactions, in contrast to Pyrex, Ca-montmorillonite, Fe-bearing montmorillonite, hematite, synthetic pyrite, and magnetite. The dependence of the rate of acetic acid decarboxylation on the surface area of pyrite per unit solution volume was also studied. The results show that the decarboxylation of acetic acid and acetate is catalyzed heterogeneously, with the cleavage of the C-C bond occurring while the acetate molecule is adsorbed onto a surface. Entropies and enthalpies of activation obtained from these experiments are compatible with the isokinetic relationship established previously for acetic acid and acetate under similar experimental conditions, indicating the existence of a common rate-determining step. Experimental evidence indicates that oxidation of acetic acid can occur with hematite and defected magnetite. These oxidative decomposition reactions differ from the decarboxylation reaction in that CO 2 and polycondensates are produced instead of CO 2 and CH 4.

  12. Conducting MWNT/poly (vinyl acetate) Composite Nanofibers by Electrospinning

    SciTech Connect

    Wang,G.; Tan, Z.; Liu, X.; Chawda, S.; Koo, J.; Samuilov, V.; Dudley, M.

    2006-01-01

    Electrospinning is a relatively simple and versatile method to produce polymer nanofibres and their composites. In this work, functionalized multiwalled carbon nanotubes (f-MWNTs) were used for the fabrication of conducting nanocomposite fibres, in comparison with the composite nanofibres made of unfunctionalized MWNTs (u-MWNTs). Our results showed that the addition of f-MWNTs could improve the dispersion of carbon nanotubes in the polymer solution and therefore result in composite nanofibres with uniform diameters by electrospinning. Alignment of the composite nanofibres was achieved by using a rotating drum as the collector. F-MWNTs were found to align parallel to the axis direction of the nanofibres. DC electrical properties of a single composite fibre were investigated at room temperature as well as cryogenic states (100-300 K). An electrical percolation phenomenon was observed for nanofibres with different mass fractions of MWNTs. It was shown that the conductivity of the material could be significantly improved above the percolation threshold. The conductivity could be of several orders of magnitude higher than the pure PVAc.

  13. Compliant intracortical implants reduce strains and strain rates in brain tissue in vivo

    NASA Astrophysics Data System (ADS)

    Sridharan, Arati; Nguyen, Jessica K.; Capadona, Jeffrey R.; Muthuswamy, Jit

    2015-06-01

    Objective. The objective of this research is to characterize the mechanical interactions of (1) soft, compliant and (2) non-compliant implants with the surrounding brain tissue in a rodent brain. Understanding such interactions will enable the engineering of novel materials that will improve stability and reliability of brain implants. Approach. Acute force measurements were made using a load cell in n = 3 live rats, each with 4 craniotomies. Using an indentation method, brain tissue was tested for changes in force using established protocols. A total of 4 non-compliant, bare silicon microshanks, 3 non-compliant polyvinyl acetate (PVAc)-coated silicon microshanks, and 6 compliant, nanocomposite microshanks were tested. Stress values were calculated by dividing the force by surface area and strain was estimated using a linear stress-strain relationship. Micromotion effects from breathing and vascular pulsatility on tissue stress were estimated from a 5 s interval of steady-state measurements. Viscoelastic properties were estimated using a second-order Prony series expansion of stress-displacement curves for each shank. Main results. The distribution of strain values imposed on brain tissue for both compliant nanocomposite microshanks and PVAc-coated, non-compliant silicon microshanks were significantly lower compared to non-compliant bare silicon shanks. Interestingly, step-indentation experiments also showed that compliant, nanocomposite materials significantly decreased stress relaxation rates in the brain tissue at the interface (p < 0.05) compared to non-compliant silicon and PVAc-coated silicon materials. Furthermore, both PVAc-coated non-compliant silicon and compliant nanocomposite shanks showed significantly reduced (by 4-5 fold) stresses due to tissue micromotion at the interface. Significance. The results of this study showed that soft, adaptive materials reduce strains and strain rates and micromotion induced stresses in the surrounding brain tissue. Understanding the material behavior at the site of tissue contact will help to improve neural implant design.

  14. Synthesis and characterization of polyvinyl alcohol based multiwalled carbon nanotube nanocomposites

    NASA Astrophysics Data System (ADS)

    Malikov, E. Y.; Muradov, M. B.; Akperov, O. H.; Eyvazova, G. M.; Puskás, R.; Madarász, D.; Nagy, L.; Kukovecz, Á.; Kónya, Z.

    2014-07-01

    Multiwalled carbon nanotubes were synthesized by chemical vapor deposition over an Fe-Co/alumina catalyst. Nanotubes were then oxidized and grafted with polyvinyl alcohol (PVA). The obtained nanostructure was characterized by Raman spectroscopy, XRD, FTIR, EDX, SEM, TEM and TGA methods. FTIR confirmed the presence of the characteristic peaks of the anticipated ester group. The formation of polymer nanocomposites based on polyvinyl alcohol and multiwalled carbon nanotubes was confirmed by SEM and TEM. High resolution electron micrographs revealed that the primary binding sites for PVA grafting are the sidewall defects of the nanotubes. The novelty of this work is the use of the Fischer esterification reaction for creating the permanent link between the nanotubes and the PVA matrix.

  15. In-situ cross linking of polyvinyl alcohol. [application to battery separator films

    NASA Technical Reports Server (NTRS)

    Philipp, W. H.; Hsu, L. C.; Sheibley, D. W. (inventors)

    1981-01-01

    A method of producing a crosslinked polyvinyl alcohol structure, such as a battery separator membrane or electrode envelope is described. An aqueous solution of a film-forming polyvinyl alcohol is admixed with an aldehyde crosslinking agent a basic pH to inhibit crosslinking. The crosslinking agent, perferably a dialdehyde such as glutaraldehyde, is used in an amount of from about 1/2 to about 20% of the theoretical amount required to crosslink all of the hydroxyl groups of the polymer. The aqueous admixture is formed into a desired physical shape, such as by casting a sheet of the solution. The sheet is then dried to form a self-supporting film. Crosslinking is then effected by immersing the film in aqueous acid solution. The resultant product has excellent properties for use as a battery separator.

  16. Oxidation of indole-3-acetic acid to oxindole-3-acetic acid by an enzyme preparation from Zea mays

    NASA Technical Reports Server (NTRS)

    Reinecke, D. M.; Bandurski, R. S.

    1988-01-01

    Indole-3-acetic acid is oxidized to oxindole-3-acetic acid by Zea mays tissue extracts. Shoot, root, and endosperm tissues have enzyme activities of 1 to 10 picomoles per hour per milligram protein. The enzyme is heat labile, is soluble, and requires oxygen for activity. Cofactors of mixed function oxygenase, peroxidase, and intermolecular dioxygenase are not stimulatory to enzymic activity. A heat-stable, detergent-extractable component from corn enhances enzyme activity 6- to 10-fold. This is the first demonstration of the in vitro enzymic oxidation of indole-3-acetic acid to oxindole-3-acetic acid in higher plants.

  17. Conserving Waterlogged Rope: A Review of Traditional Methods and Experimental Research with Polyethylene Glycol 

    E-print Network

    McCaskill, Jennifer R.

    2010-01-16

    Conservation Research Laboratory DBTDA dibutyltin diacetate EDTA ethylenediaminetetraacetic acid INA Institute of Nautical Archaeology MTMS methyltrimethoxysilane PEG polyethylene glycol PVA polyvinyl acetate PVP polyvinyl pyrrolidone PVOH polyvinyl...

  18. 40 CFR Table 2 to Subpart B of... - MON Source Categories

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...Production. Polyester Resins Production. Polymerized Vinylidene Chloride Production. Polymethyl Methacrylate Resins Production. Polyvinyl Acetate Emulsions Production. Polyvinyl Alcohol Production. Polyvinyl Butyral Production....

  19. 40 CFR Table 2 to Subpart B of... - MON Source Categories

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...Production. Polyester Resins Production. Polymerized Vinylidene Chloride Production. Polymethyl Methacrylate Resins Production. Polyvinyl Acetate Emulsions Production. Polyvinyl Alcohol Production. Polyvinyl Butyral Production....

  20. Preparation of the poly(vinyl alcohol)/layered double hydroxide nanocomposite

    SciTech Connect

    Li Baoguang; Hu Yuan; Zhang Rui; Chen Zuyao; Fan Weicheng

    2003-10-01

    Intercalated nanocomposite based on Mg, Al layered double hydroxide (LDH) and poly(vinyl alcohol) (PVA) was prepared using exfoliation-adsorption technique, and characterized by X-ray diffraction and thermal gravimetric analysis. The results suggest that the intercalated species are formed via the re-aggregation of the delaminated LDH lamellar with the interlayer spacing 14.5 A, and the thermal stability of the nanocomposite improved compared with the original PVA.

  1. Disruption of the protective properties of the polyvinyl chloride coating under the effect of microorganisms

    SciTech Connect

    Mogil'nitskii, G.M.; Sagatelyan, R.T.; Kutishcheva, T.N.; Zhukova, S.V.; Kerimov, S.I.; Parfenova, T.B.

    1987-09-01

    The presence of sulfate-reducing bacteria results in a reduction of the protective properties of polyvinyl chloride (PVC) film coatings. The authors examine the effect of other types of soil microorganisms. Investigations were carried out with the cultures of bacteria Pseudomonas fluorescens B-22 and fungus Aspergillus niger van Tieghem F-1119 which are almost always present in corrosion regions in the routes of transmission pipelines. The microorganisms were grown in a mineral medium with glucose (Ps. fluorescens) and sucrose (A. niger).

  2. Edge-enhanced imaging with polyvinyl alcohol/acrylamide photopolymer gratings

    NASA Astrophysics Data System (ADS)

    Márquez, Andrés; Neipp, Cristian; Beléndez, Augusto; Gallego, Sergi; Ortun~O, Manuel; Pascual, Inmaculada

    2003-09-01

    We demonstrate edge-enhanced imaging produced by volume phase gratings recorded on a polyvinyl alcohol/acrylamide photopolymer. Bragg diffraction, exhibited by volume gratings, modifies the impulse response of the imaging system, facilitating spatial filtering operations with no need for a physical Fourier plane. We demonstrate that Kogelnik's coupled-wave theory can be used to calculate the transfer function for the transmitted and the diffracted orders. The experimental and simulated results agree, and they demonstrate the feasibility of our proposal.

  3. Film dosimeters based on methylene blue and methyl orange in polyvinyl alcohol

    SciTech Connect

    Chung, W.H. . Dept. of Physics); Miller, A. )

    1994-05-01

    Polyvinyl alcohol (PVA) films containing methylene blue and methyl orange are useful as gamma and electron radiation dosimeters. Absorbed doses should not exceed 40 kGy for methylene blue and 500 kGy for methyl orange. Because PVA is water-soluble, the films may be made without toxic solvents. The effects of irradiation temperature and humidity on the radiation response of the dosimeter films are discussed.

  4. Synthesis and regeneration of lead (IV) acetate

    SciTech Connect

    Boyle, T.J.; Al-Shareef, H.N.; Moore, G.J.

    1996-11-01

    Lead acetate [Pb(O{sub 2}CMe){sub 4}] was easily synthesized from a warm solution of Pb{sub 3}O{sub 4}, HO{sub 2}CMe and O(OCMe){sub 2} following literature preparations when the appropriate measures to minimize water contamination were followed. Furthermore, Pb(O{sub 2}CMe){sub 4} which has been decomposed (evidenced by the appearance of a purple color due to oxidation) can be regenerated using a similar preparatory route. Introduction of Pb(O{sub 2}CMe){sub 4} from the two routes outlined above into the IMO process for production of PZT thin films gave films with comparable ferroelectric properties to commercially available Pb(O{sub 2}CMe){sub 4} precursors. However, the freshly synthesized material yields PZT films with better properties compared to the recycled material.

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

    PubMed Central

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

    2012-01-01

    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 ? cm2 and 0.83, respectively. PMID:24958543

  6. Antibacterial silver nanoparticles in polyvinyl alcohol/sodium alginate blend produced by gamma irradiation.

    PubMed

    Eghbalifam, Naeimeh; Frounchi, Masoud; Dadbin, Susan

    2015-09-01

    Polyvinyl alcohol/sodium alginate/nano silver (PVA/SA/Ag) composite films were made by solution casting method. Gamma irradiation was used to synthesize silver nanoparticles in situ via reduction of silver nitrate without using harmful chemical agents for biomedical applications. UV-vis and XRD results demonstrated that spherical silver nanoparticles were produced even at low irradiation dose of 5kGy. By increasing irradiation dose, more nanoparticles were synthesized while no PVA hydrogel was formed up to 15kGy. Also the size of nanoparticles was reduced with increasing gamma dose evidenced by higher release rate of silver nanoparticles in lukewarm water and SEM images. Comparing SEM images with DLS results indicated good performance of PVA/SA as an efficient stabilizer in preventing agglomeration of the silver nanoparticles. Good miscibility of polyvinyl alcohol and sodium alginate observed on the SEM images was supported with FTIR spectroscopy. Upon addition of sodium alginate to polyvinyl alcohol and increasing silver nanoparticles, the melting peak shifted to lower temperature and crystallinity percent was decreased. Addition of sodium alginate led to remarkable increase in rigidity of PVA. The composites exhibited strong antibacterial activity against Staphylococcus aureus and Escherichia coli even at very low level of silver nanoparticles. PMID:26123816

  7. Heterogeneous catalyst for the production of acetic anhydride from methyl acetate

    DOEpatents

    Ramprasad, D.; Waller, F.J.

    1999-04-06

    This invention relates to a process for producing acetic anhydride by the reaction of methyl acetate, carbon monoxide, and hydrogen at elevated temperatures and pressures in the presence of an alkyl halide and a heterogeneous, bifunctional catalyst that contains an insoluble polymer having pendant quaternized phosphine groups, some of which phosphine groups are ionically bonded to anionic Group VIII metal complexes, the remainder of the phosphine groups being bonded to iodide. In contrast to prior art processes, no accelerator (promoter) is necessary to achieve the catalytic reaction and the products are easily separated from the catalyst by filtration. The catalyst can be recycled for consecutive runs without loss in activity. Bifunctional catalysts for use in carbonylating dimethyl ether are also provided.

  8. Heterogeneous catalyst for the production of acetic anhydride from methyl acetate

    DOEpatents

    Ramprasad, Dorai (Allentown, PA); Waller, Francis Joseph (Allentown, PA)

    1999-01-01

    This invention relates to a process for producing acetic anhydride by the reaction of methyl acetate, carbon monoxide, and hydrogen at elevated temperatures and pressures in the presence of an alkyl halide and a heterogeneous, bifunctional catalyst that contains an insoluble polymer having pendant quaternized phosphine groups, some of which phosphine groups are ionically bonded to anionic Group VIII metal complexes, the remainder of the phosphine groups being bonded to iodide. In contrast to prior art processes, no accelerator (promoter) is necessary to achieve the catalytic reaction and the products are easily separated from the catalyst by filtration. The catalyst can be recycled for consecutive runs without loss in activity. Bifunctional catalysts for use in carbonylating dimethyl ether are also provided.

  9. Formulation and evaluation of an in situ gel forming system for controlled delivery of triptorelin acetate.

    PubMed

    Abashzadeh, Sh; Dinarvand, R; Sharifzadeh, M; Hassanzadeh, G; Amini, M; Atyabi, F

    2011-11-20

    The novel physical hydrogels composed of chitosan or its water soluble derivatives such as carboxymethyl chitosan (CMCh) and sodium carboxymethyl chitosan (NaCMCh) and opened ring polyvinyl pyrrolidone (OP-PVP) were used as a controlled delivery system for triptorelin acetate, a luteinizing-releasing hormone agonist. The in situ gel forming system designed according to physical interactions such as chains entanglements and hydrophilic attractions especially h-bonds of chitosan and/or NaCMCh and OR-PVP. In order to increase in situ gel forming rate the chitosan microspheres prepared through spray drying technique. The chitosan or NaCMCh/OR-PVP blends prepared at different ratios (0.05, 0.10, 0.12, 0.16, 0.20 and 0.24) and suspended in sesame oil as non-aqueous vehicle at different solid content (10-30%). The suitable ratio of polymers with faster in situ gel forming rate was selected for in vivo studies. The gel formation and drug release from the system was evaluated both in vitro and in vivo. In vitro and in vivo results were compared with Diphereline SR 3.75mg, a commercially available controlled delivery system of triptorelin. In vitro release studies showed a sustained release profile for about 192h with first order kinetics. In vivo studies on male rats by determination of serum testosterone were confirmed the acceptable performance of in situ gel forming system compared with Diphereline SR in decreasing the serum testosterone level for 35days, demonstrating the potential of the novel in situ gel forming system for controlled delivery of peptides. PMID:21946260

  10. 21 CFR 522.2477 - Trenbolone acetate and estradiol.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...DRUGS, FEEDS, AND RELATED PRODUCTS IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL...trenbolone acetate and 24 mg estradiol (one implant consisting of 6 pellets, each pellet...trenbolone acetate and 4 mg estradiol) per implant dose. (B) 120 mg trenbolone...

  11. 21 CFR 522.2477 - Trenbolone acetate and estradiol.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... § 522.2477, see the List of CFR Sections Affected, which appears in the Finding Aids section of the... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Trenbolone acetate and estradiol. 522.2477 Section... § 522.2477 Trenbolone acetate and estradiol. (a) (b) Sponsors. See sponsors in § 510.600(c) of...

  12. Transition-Metal-Catalyzed Carbonylation of Methyl Acetate.

    ERIC Educational Resources Information Center

    Polichnowski, S. W.

    1986-01-01

    Presents a study of the rhodium-catalyzed, ioding-promoted carbonylation of methyl acetate. This study provides an interesting contrast between the carbonylation of methyl acetate and the carbonylation of methanol when similar rhodium/iodine catalyst systems are used. (JN)

  13. 21 CFR 520.1341 - Megestrol acetate tablets.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Megestrol acetate tablets. 520.1341 Section 520.1341 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS ORAL DOSAGE FORM NEW ANIMAL DRUGS § 520.1341 Megestrol acetate tablets. (a) Specifications. Each...

  14. 21 CFR 522.2477 - Trenbolone acetate and estradiol.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... § 522.2477, see the List of CFR Sections Affected, which appears in the Finding Aids section of the... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Trenbolone acetate and estradiol. 522.2477 Section... § 522.2477 Trenbolone acetate and estradiol. (a) (b) Sponsors. See sponsors in § 510.600(c) of...

  15. Oxidation of Indole-3-acetic Acid and Oxindole-3-acetic Acid to 2,3-Dihydro-7-hydroxy-2-oxo-1H Indole-3-acetic Acid-7?-O-?-d-Glucopyranoside in Zea mays Seedlings 1

    PubMed Central

    Nonhebel, Heather M.; Bandurski, Robert S.

    1984-01-01

    Radiolabeled oxindole-3-acetic acid was metabolized by roots, shoots, and caryopses of dark grown Zea mays seedlings to 2,3-dihydro-7-hydroxy-2-oxo-1H indole-3-acetic acid-7?-O-?-d-glycopyranoside with the simpler name of 7-hydroxyoxindole-3-acetic acid-glucoside. This compound was also formed from labeled indole-3-acetic acid supplied to intact seedlings and root segments. The glucoside of 7-hydroxyoxindole-3-acetic acid was also isolated as an endogenous compound in the caryopses and shoots of 4-day-old seedlings. It accumulates to a level of 4.8 nanomoles per plant in the kernel, more than 10 times the amount of oxindole-3-acetic acid. In the shoot it is present at levels comparable to that of oxindole-3-acetic acid and indole-3-acetic acid (62 picomoles per shoot). We conclude that 7-hydroxyoxindole-3-acetic acid-glucoside is a natural metabolite of indole-3-acetic acid in Z. mays seedlings. From the data presented in this paper and in previous work, we propose the following route as the principal catabolic pathway for indole-3-acetic acid in Zea seedlings: Indole-3-acetic acid ? Oxindole-3-acetic acid ? 7-Hydroxyoxindole-3-acetic acid ? 7-Hydroxyoxindole-3-acetic acid-glucoside. PMID:11540902

  16. Oxidation of indole-3-acetic acid and oxindole-3-acetic acid to 2,3-dihydro-7-hydroxy-2-oxo-1H indole-3-acetic acid-7'-O-beta-D-glucopyranoside in Zea mays seedlings

    NASA Technical Reports Server (NTRS)

    Nonhebel, H. M.; Bandurski, R. S.

    1984-01-01

    Radiolabeled oxindole-3-acetic acid was metabolized by roots, shoots, and caryopses of dark grown Zea mays seedlings to 2,3-dihydro-7-hydroxy-2-oxo-1H indole-3-acetic acid-7'-O-beta-D-glycopyranoside with the simpler name of 7-hydroxyoxindole-3-acetic acid-glucoside. This compound was also formed from labeled indole-3-acetic acid supplied to intact seedlings and root segments. The glucoside of 7-hydroxyoxindole-3-acetic acid was also isolated as an endogenous compound in the caryopses and shoots of 4-day-old seedlings. It accumulates to a level of 4.8 nanomoles per plant in the kernel, more than 10 times the amount of oxindole-3-acetic acid. In the shoot it is present at levels comparable to that of oxindole-3-acetic acid and indole-3-acetic acid (62 picomoles per shoot). We conclude that 7-hydroxyoxindole-3-acetic acid-glucoside is a natural metabolite of indole-3-acetic acid in Z. mays seedlings. From the data presented in this paper and in previous work, we propose the following route as the principal catabolic pathway for indole-3-acetic acid in Zea seedlings: Indole-3-acetic acid --> Oxindole-3-acetic acid --> 7-Hydroxyoxindole-3-acetic acid --> 7-Hydroxyoxindole-3-acetic acid-glucoside.

  17. Measurement of the rates of oxindole-3-acetic acid turnover, and indole-3-acetic acid oxidation in Zea mays seedlings

    NASA Technical Reports Server (NTRS)

    Nonhebel, H. M.; Bandurski, R. S. (Principal Investigator)

    1986-01-01

    Oxindole-3-acetic acid is the principal catabolite of indole-3-acetic acid in Zea mays seedlings. In this paper measurements of the turnover of oxindole-3-acetic acid are presented and used to calculate the rate of indole-3-acetic acid oxidation. [3H]Oxindole-3-acetic acid was applied to the endosperm of Zea mays seedlings and allowed to equilibrate for 24 h before the start of the experiment. The subsequent decrease in its specific activity was used to calculate the turnover rate. The average half-life of oxindole-3-acetic acid in the shoots was found to be 30 h while that in the kernels had an average half-life of 35h. Using previously published values of the pool sizes of oxindole-3-acetic acid in shoots and kernels from seedlings of the same age and variety, and grown under the same conditions, the rate of indole-3-acetic acid oxidation was calculated to be 1.1 pmol plant-1 h-1 in the shoots and 7.1 pmol plant-1 h-1 in the kernels.

  18. 76 FR 32366 - Determination That ORLAAM (Levomethadyl Acetate Hydrochloride) Oral Solution, 10 Milligrams...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-06-06

    ...DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and...Levomethadyl Acetate Hydrochloride) Oral Solution, 10 Milligrams/Milliliter...acetate hydrochloride (HCl)) oral solution, 10 milligrams (mg...for levomethadyl acetate HCl oral solution, 10 mg/mL, if...

  19. 40 CFR 180.1258 - Acetic acid; exemption from the requirement of a tolerance.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 2011-07-01 false Acetic acid; exemption from the requirement...From Tolerances § 180.1258 Acetic acid; exemption from the requirement...residues of the biochemical pesticide acetic acid when used as a...

  20. Micelles Protect and Concentrate Activated Acetic Acid

    NASA Astrophysics Data System (ADS)

    Todd, Zoe; House, C.

    2014-01-01

    As more and more exoplanets are discovered and the habitability of such planets is considered, one can turn to searching for the origin of life on Earth in order to better understand what makes a habitable planet. Activated acetic acid, or methyl thioacetate, has been proposed to be central to the origin of life on Earth, and also as an important energy currency molecule in early cellular evolution. We have investigated the hydrolysis of methyl thioacetate under various conditions. Its uncatalyzed rate of hydrolysis is about three orders of magnitude faster (K = 0.00663 s^-1; 100°C, pH 7.5, concentration = 0.33mM) than published rates for its catalyzed production making it unlikely to accumulate under prebiotic conditions. However, we also observed that methyl thioacetate was protected from hydrolysis when inside its own hydrophobic droplets. We found that methyl thioacetate protection from hydrolysis was also possible in droplets of hexane and in the membranes of nonanoic acid micelles. Thus, the hydrophobic regions of prebiotic micelles and early cell membranes could have offered a refuge for this energetic molecule increasing its lifetime in close proximity to the reactions for which it would be needed. Methyl thioacetate could thus be important for the origin of life on Earth and perhaps for better understanding the potential habitability of other planets.

  1. Formate and acetate in monsoon rainwater of Agra, India

    SciTech Connect

    Kumar, N.; Kulshrestha, U.C.; Saxena, A.; Kumari, K.M.; Srivastava, S.S. )

    1993-03-20

    Formate and acetate concentrations were estimated using ion chromatography in 19 precipitation samples collected on an eventwise basis during the monsoon season (July through September), 1991, at Dayalbagh, Agra. Volume-weighted average (VWA) concentrations for formate and acetate were 5.8 and 6.55 [mu]molL[sup [minus]1], respectively. The VWA hydrogen ion concentration was 0.084 [mu]eq L[sub [minus]1] (pH 7.07) and the correlation coefficient between the two ions was 0.85. The average formate to acetate ratio was low (0.88), possibly due to an increase in acetate contribution from direct emissions associated with heavy vehicular traffic load and/or indirect acetate formation by alkaline hydrolysis of PAN. Widespread local use of biomass as a domestic fuel may also contribute acetate. In 4 of the 19 precipitation events studied, higher values of both species were recorded. Contributions from soil in addition to vegetation, were suspected in these samples. Inputs from soil and combustion activities were supported by correlations among formate, acetate and Ca[sup 2+] (terrigenous species), K[sup +], SO[sub 4][sup 2[minus

  2. A Search for Methyl Acetate in Hot Cores

    NASA Astrophysics Data System (ADS)

    Kelley, Matthew; Braakman, Rogier; Blake, Geoffrey

    2006-10-01

    We propose to search for methyl acetate, CH3COOCH3, in high mass hot cores. Methyl acetate is possibly synthesized through multiple reaction pathways from molecules previously detected in hot cores, most notably from acetic acid and methanol via esterification. Esterification, beyond the formation of methyl formate, has not yet been observed in the ISM. The project is already underway in nothern sources based on millimeter data from the Caltech Submillimeter Observatory (CSO). We hope to study the chemically rich southern source G327.3 (decl B1950=-54.49'15.6"), amongst others, using MOPRA and to search for acetic acid and methyl acetate. Observations are supported by laboratory studies of methyl acetate in the 3 mm and 1 mm and successful spectral fitting by the Blake group at Caltech. If detected, methyl acetate, consisting of 11 atoms, would be one of the larger complex organic molecules detected in the interstellar medium and could point to previously unconsidered reaction mechanisms.

  3. The Effects of Acetate Buffer Concentration on Lysozyme Solubility

    NASA Technical Reports Server (NTRS)

    Forsythe, Elizabeth L.; Pusey, Marc L.

    1996-01-01

    The micro-solubility column technique was employed to systematically investigate the effects of buffer concentration on tetragonal lysozyme solubility. While keeping the NaCl concentrations constant at 2%, 3%, 4%, 5% and 7%, and the pH at 4.0, we have studied the solubility of tetragonal lysozyme over an acetate buffer concentration range of 0.01M to 0.5M as a function of temperature. The lysozyme solubility decreased with increasing acetate concentration from 0.01M to 0.1M. This decrease may simply be due to the net increase in solvent ionic strength. Increasing the acetate concentration beyond 0.1M resulted in an increase in the lysozyme solubility, which reached a peak at - 0.3M acetate concentration. This increase was believed to be due to the increased binding of acetate to the anionic binding sites of lysozyme, preventing their occupation by chloride. In keeping with the previously observed reversal of the Hoffmeister series for effectiveness of anions in crystallizing lysozyme, acetate would be a less effective precipitant than chloride. Further increasing the acetate concentration beyond 0.3M resulted in a subsequent gradual decrease in the lysozyme solubility at all NaCl concentrations.

  4. Crystal structure of a mixed solvated form of amoxapine acetate

    PubMed Central

    Bhardwaj, Rajni M.; Raval, Vishal; Oswald, Iain D. H.; Florence, Alastair J.

    2015-01-01

    The mixed solvated salt 4-(2-chloro­dibenzo[b,f][1,4]oxazepin-11-yl)piperazin-1-ium acetate–acetic acid–cyclo­hexane (2/2/1), C17H17ClN3O+·C2H3O2 ?·C2H4O2·0.5C6H12, crystallizes with one mol­ecule of protonated amoxapine (AXPN), an acetate anion and a mol­ecule of acetic acid together with half a mol­ecule of cyclo­hexane. In the centrosymmetric crystal, both enanti­omers of the protonated AXPN mol­ecule stack alternatively along [001]. Acetate anions connect the AXPN cations through N—H?O hydrogen bonding in the [010] direction, creating a sheet lying parallel to (100). The acetic acid mol­ecules are linked to the acetate anions via O—H?O hydrogen bonds within the sheets. Within the sheets there are also a number of C—H?O hydrogen bonds present. The cyclo­hexane solvent mol­ecules occupy the space between the sheets. PMID:25878802

  5. Increased brain uptake and oxidation of acetate in heavy drinkers

    PubMed Central

    Jiang, Lihong; Gulanski, Barbara Irene; De Feyter, Henk M.; Weinzimer, Stuart A.; Pittman, Brian; Guidone, Elizabeth; Koretski, Julia; Harman, Susan; Petrakis, Ismene L.; Krystal, John H.; Mason, Graeme F.

    2013-01-01

    When a person consumes ethanol, the body quickly begins to convert it to acetic acid, which circulates in the blood and can serve as a source of energy for the brain and other organs. This study used 13C magnetic resonance spectroscopy to test whether chronic heavy drinking is associated with greater brain uptake and oxidation of acetic acid, providing a potential metabolic reward or adenosinergic effect as a consequence of drinking. Seven heavy drinkers, who regularly consumed at least 8 drinks per week and at least 4 drinks per day at least once per week, and 7 light drinkers, who consumed fewer than 2 drinks per week were recruited. The subjects were administered [2-13C]acetate for 2 hours and scanned throughout that time with magnetic resonance spectroscopy of the brain to observe natural 13C abundance of N-acetylaspartate (NAA) and the appearance of 13C-labeled glutamate, glutamine, and acetate. Heavy drinkers had approximately 2-fold more brain acetate relative to blood and twice as much labeled glutamate and glutamine. The results show that acetate transport and oxidation are faster in heavy drinkers compared with that in light drinkers. Our finding suggests that a new therapeutic approach to supply acetate during alcohol detoxification may be beneficial. PMID:23478412

  6. Computerized image analysis for acetic acid induced intraepithelial lesions

    NASA Astrophysics Data System (ADS)

    Li, Wenjing; Ferris, Daron G.; Lieberman, Rich W.

    2008-03-01

    Cervical Intraepithelial Neoplasia (CIN) exhibits certain morphologic features that can be identified during a visual inspection exam. Immature and dysphasic cervical squamous epithelium turns white after application of acetic acid during the exam. The whitening process occurs visually over several minutes and subjectively discriminates between dysphasic and normal tissue. Digital imaging technologies allow us to assist the physician analyzing the acetic acid induced lesions (acetowhite region) in a fully automatic way. This paper reports a study designed to measure multiple parameters of the acetowhitening process from two images captured with a digital colposcope. One image is captured before the acetic acid application, and the other is captured after the acetic acid application. The spatial change of the acetowhitening is extracted using color and texture information in the post acetic acid image; the temporal change is extracted from the intensity and color changes between the post acetic acid and pre acetic acid images with an automatic alignment. The imaging and data analysis system has been evaluated with a total of 99 human subjects and demonstrate its potential to screening underserved women where access to skilled colposcopists is limited.

  7. Methane Production and Syntrophic Acetate Oxidation in the Florida Everglades

    NASA Astrophysics Data System (ADS)

    Holmes, M. E.; Chanton, J.; Bae, H.; Ogram, A.

    2012-12-01

    Methane production pathways in the Florida Everglades are influenced by factors such as nutrient levels, H2 concentrations, and temperature. Syntrophic acetate oxidizers can outcompete methanogens for acetate when conditions are right (high temperatures and low H2). During syntrophic acetate oxidation (SAO), which becomes more exergonic with increasing temperature, acetate is oxidized to carbon dioxide and H2, which can be utilized to produce methane via CO2 reduction. Everglades soil from along a nutrient gradient was incubated at 25°C and 45°C. The shift to the CO2 reduction pathway for methane formation that would be expected in high temperature incubations due to SAO should result in a decrease in ?13C-CH4 and increase in ?2H-CH4. Instead, we observed higher ?13C and lower ?2H in the methane produced in high temperature incubations. The higher than expected ?13C may be partly explained by lower kinetic isotope effects caused by temperature. Coupling between the syntrophic acetate oxidizers and the CO2 reducers, whereby isotopically light hydrogen from acetate is used in methane formation could lower ?2H-CH4. Separate experiments using 13C-labelled acetate revealed that potential SAO activity is low in soils collected from the Everglades.

  8. Stable carbon isotope discrimination in rice field soil during acetate turnover by syntrophic acetate oxidation or acetoclastic methanogenesis

    NASA Astrophysics Data System (ADS)

    Conrad, Ralf; Klose, Melanie

    2011-03-01

    Rice fields are an important source for the greenhouse gas methane. In Italian rice field soil CH 4 is produced either by hydrogenotrophic and acetoclastic methanogenesis, or by hydrogenotrophic methanogenesis and syntrophic acetate oxidation when temperatures are below and above about 40-45 °C, respectively. In order to see whether these acetate consumption pathways differently discriminate the stable carbon isotopes of acetate, we measured the ? 13C of total acetate and acetate-methyl as well as the ? 13C of CO 2 and CH 4 in rice field soil that had been pre-incubated at 45 °C and then shifted to different temperatures between 25 and 50 °C. Acetate transiently accumulated to about 6 mM, which is about one-third of the amount of CH 4 produced, irrespective of the incubation temperature and the CH 4 production pathway involved. However, the patterns of ? 13C of the CH 4 and CO 2 produced were different at low (25, 30, 35 °C) versus high (40, 45, 50 °C) temperatures. These patterns were consistent with CH 4 being exclusively formed by hydrogenotrophic methanogenesis at high temperatures, and by a combination of acetoclastic and hydrogenotrophic methanogenesis at low temperatures. The patterns of ? 13C of total acetate and acetate-methyl were also different at high versus low temperatures, indicating the involvement of different pathways of production and consumption of acetate at the two temperature regimes. Isotope fractionation during consumption of the methyl group of acetate was more pronounced at low ( ? = 1.010-1.025) than at high ( ? = 1.0-1.01) temperatures indicating that acetoclastic methanogenesis exhibits a stronger isotope effect than syntrophic acetate oxidation. Small amounts of propionate also transiently accumulated and were analyzed for ? 13C. The ? 13C values slightly increased (by about 10‰) during production and consumption of propionate, but were not affected by incubation temperature. Collectively, our results showed distinct isotope discrimination for different paths of acetate (and propionate) production and consumption, albeit differences were only small, and discrimination between methanogenic and syntrophic acetate consumption in nature may be difficult to detect.

  9. Conducting polymer blends: Polypyrrole and polythiophene blends with polystyrene, polycarbonate resin, poly(vinyl alcohol) and poly(vinyl methyl ketone)

    SciTech Connect

    Wang, H.L.

    1992-01-01

    Various aromatic compounds can be polymerized by electrochemical oxidation in solution containing a supporting electrolyte. Most studies have been devoted to polypyrrole and polythiophene. In situ doping during electrochemical polymerization yields free standing conductive polymer film. One major approach to making conducting polymer blends is electrochemical synthesis after coating the host polymer on a platinum electrode. In the electrolysis of pyrrole or thiophene monomer, using (t-Bu[sub 4]N)BF[sub 4] as supporting electrolyte, and acetonitrile as solvent, monomer can diffuse through the polymer film, to produce a polypyrrole or polythiophene blend in the film. Doping occurs along with polymerization to form a conducting polymer alloy. The strongest molecular interaction in polymers, and one that is central to phase behavior, is hydrogen bonding. This mixing at the molecular level enhances the degree of miscibility between two polymers and results in macroscopic properties indicative of single phase behavior. In this dissertation, the authors describes the syntheses of conducting polymer blends: polypyrrole and polythiophene blends with polystyrene, poly(bisphenol-A-carbonate), polyvinyl alcohol and poly(vinyl methyl ketone). The syntheses are performed both electrochemically and chemically. Characterization of these blends was carried out by Fourier Transform Infrared spectroscopy, Differential Scanning Calorimetry, Thermogravimetric Analysis, Scanning Electron Microscopy, and X-ray diffraction. Percolating threshold conductivities occur from 7% to 20% for different polymer blends. The low threshold conductivity is attributed to blend homogeneity enhanced by hydrogen bonding between the carbonyl group in the insulating polymer and the N-H group in polypyrrole. Thermal stability, environmental stability, mechanical properties, crystallinity and morphological structure are also discussed. The authors have also engaged in the polymerization of imidazoles.

  10. Selective Cross-Coupling of Organic Halides with Allylic Acetates

    PubMed Central

    Anka-Lufford, Lukiana L.; Prinsell, Michael R.

    2012-01-01

    A general protocol for the coupling of haloarenes with a variety of allylic acetates is presented. Strengths of the method are a tolerance for electrophilic (ketone, aldehyde) and acidic (sulfonamide, trifluoroacetamide) substrates and the ability to couple with a variety of substituted allylic acetates. Secondary alkyl bromides can also be allylated under slightly modified conditions, demonstrating the generality of the approach. Finally, the coupling of a reactive vinyl halide could be achieved by the use of a very hindered ligand and more reactive, branched allylic acetates. PMID:23095043

  11. Clostridiumm ljungdahlii, an anaerobic ethanol and acetate producing microorganism

    DOEpatents

    Gaddy, J.L.; Clausen, E.C.

    1992-12-22

    A newly discovered microorganism was isolated in a biologically pure culture and designated Clostridium ljungdahlii, having the identifying characteristics of ATCC No. 49587. Cultured in an aqueous nutrient medium under anaerobic conditions, this microorganism is capable of producing ethanol and acetate from CO and H[sub 2]O and/or CO[sub 2] and H[sub 2] in synthesis gas. Under optimal growth conditions, the microorganism produces acetate in preference to ethanol. Conversely, under non-growth conditions, ethanol production is favored over acetate. 3 figs.

  12. Clostridiumm ljungdahlii, an anaerobic ethanol and acetate producing microorganism

    DOEpatents

    Gaddy, James L. (Fayetteville, AR); Clausen, Edgar C. (Fayetteville, AR)

    1992-01-01

    A newly discovered microorganism was isolated in a biologically pure culture and designated Clostridium ljungdahlii, having the identifying characteristics of ATCC No. 49587. Cultured in an aqueous nutrient medium under anaerobic conditions, this microorganism is capable of producing ethanol and acetate from CO and H.sub.2 O and/or CO.sub.2 and H.sub.2 in synthesis gas. Under optimal growth conditions, the microorganism produces acetate in preference to ethanol. Conversely, under non-growth conditions, ethanol production is favored over acetate.

  13. Water dispersible microbicidal cellulose acetate phthalate film

    PubMed Central

    Neurath, A Robert; Strick, Nathan; Li, Yun-Yao

    2003-01-01

    Background Cellulose acetate phthalate (CAP) has been used for several decades in the pharmaceutical industry for enteric film coating of oral tablets and capsules. Micronized CAP, available commercially as "Aquateric" and containing additional ingredients required for micronization, used for tablet coating from water dispersions, was shown to adsorb and inactivate the human immunodeficiency virus (HIV-1), herpesviruses (HSV) and other sexually transmitted disease (STD) pathogens. Earlier studies indicate that a gel formulation of micronized CAP has a potential as a topical microbicide for prevention of STDs including the acquired immunodeficiency syndrome (AIDS). The objective of endeavors described here was to develop a water dispersible CAP film amenable to inexpensive industrial mass production. Methods CAP and hydroxypropyl cellulose (HPC) were dissolved in different organic solvent mixtures, poured into dishes, and the solvents evaporated. Graded quantities of a resulting selected film were mixed for 5 min at 37°C with HIV-1, HSV and other STD pathogens, respectively. Residual infectivity of the treated viruses and bacteria was determined. Results The prerequisites for producing CAP films which are soft, flexible and dispersible in water, resulting in smooth gels, are combining CAP with HPC (other cellulose derivatives are unsuitable), and casting from organic solvent mixtures containing ?50 to ?65% ethanol (EtOH). The films are ?100 µ thick and have a textured surface with alternating protrusions and depressions revealed by scanning electron microscopy. The films, before complete conversion into a gel, rapidly inactivated HIV-1 and HSV and reduced the infectivity of non-viral STD pathogens >1,000-fold. Conclusions Soft pliable CAP-HPC composite films can be generated by casting from organic solvent mixtures containing EtOH. The films rapidly reduce the infectivity of several STD pathogens, including HIV-1. They are converted into gels and thus do not have to be removed following application and use. In addition to their potential as topical microbicides, the films have promise for mucosal delivery of pharmaceuticals other than CAP. PMID:14617380

  14. Diffusion studies of FeCl3 doped poly(vinyl alcohol) films

    NASA Astrophysics Data System (ADS)

    Sheela, T.; Ravindrachary, V.; Bhajantri, R. F.; Ismayil, Rathod, Sunil; Praveena, S. D.

    2012-06-01

    Poly(vinyl alcohol) (PVA) films doped with various mass fractions of FeCl3 were prepared by solution casting method. The diffusion studies of FeCl3 doped PVA were carried out using distilled water, rain water and sea water. The diffusion coefficient and penetration rate decreases with increasing FeCl3 concentration, which is explained by Fick's law of diffusion. The crosslinking density Ve, is calculated based on Flory-Huggins theory. The crosslinking density increases with increase in FeCl3 dopant concentration.

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

    NASA Astrophysics Data System (ADS)

    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.

  16. A relative humidity sensing probe based on etched thin-core fiber coated with polyvinyl alcohol

    NASA Astrophysics Data System (ADS)

    Sun, Hao; Yang, Zaihang; Zhou, Libin; Liu, Nan; Gang, Tingting; Qiao, Xueguang; Hu, Manli

    2015-12-01

    A relative humidity (RH) sensing probe based on etched thin-core fiber (TCF) coated with polyvinyl alcohol (PVA) is proposed and experimentally demonstrated.This sensor is constructed by splicing a section of TCF with a single mode fiber (SMF), then part of the TCF's cladding is etched by hydrofluoric acid solution and finally the tip of TCF is coated with PVA. Experimental results demonstrate that this sensor can measure the ambient RH by demodulating the power variation of reflection spectrum. The power demodulation method make this sensor can ignore the temperature cross-sensitivity and have an extensive application prospect.

  17. Preparation and characterization of poly(vinyl alcohol)/graphene nanofibers synthesized by electrospinning

    NASA Astrophysics Data System (ADS)

    Barzegar, Farshad; Bello, Abdulhakeem; Fabiane, Mopeli; Khamlich, Saleh; Momodu, Damilola; Taghizadeh, Fatemeh; Dangbegnon, Julien; Manyala, Ncholu

    2015-02-01

    We report on the synthesis and characterization of electrospun polyvinyl alcohol (PVA)/graphene nanofibers. The samples produced were characterized by Raman spectroscopy for structural and defect density analysis, scanning electron microscopy (SEM) for morphological analysis, and thermogravimetric (TGA) for thermal analysis. SEM measurements show uniform hollow PVA fibers formation and excellent graphene dispersion within the fibers, while TGA measurements show the improved thermal stability of PVA in the presence of graphene. The synthesized polymer reinforced nanofibers have potential to serve in many different applications such as thermal management, supercapacitor electrodes and biomedical materials for drug delivery.

  18. Study of polyvinyl alcohol nanofibrous membrane by electrospinning as a magnetic nanoparticle delivery approach

    NASA Astrophysics Data System (ADS)

    Ger, Tzong-Rong; Huang, Hao-Ting; Huang, Chen-Yu; Hu, Keng-Shiang; Lai, Jun-Yang; Chen, Jiann-Yeu; Lai, Mei-Feng

    2014-05-01

    Electrospinning technique was used to fabricate polyvinyl alcohol (PVA)-based magnetic biodegradable nanofibers. PVA solution was mixed with ferrofluid or magnetic nanoparticles (MNPs) powder and formed two individual nanofibrous membranes (PVA/ferrofluid and PVA/MNPs powder) by electrospinning. The surface morphology of the nanofibrous membrane was characterized by scanning electron microscopy and the magnetic properties were measured by vibrating sample magnetometer. Macrophages (RAW 264.7) were co-cultured with the nanofibrous membranes for 12, 24, and 48 h and exhibited good cell viability (>95%). Results showed that the PVA fibers would be degraded and the embedded Fe3O4 nanoparticles would be released and delivered to cells.

  19. Spectrophotometric determination of antimony with vanillylfluorone in the presence of poly(vinyl alcohol).

    PubMed

    Mori, I; Fujita, Y; Toyoda, M; Kato, K; Fujita, K; Okazaki, Y

    1991-03-01

    Antimony in the range up to 2.5 mug/ml in the final solution is determined spectrophotometrically with vanillylfluorone in the presence of poly(vinyl alcohol) in acidic media. The method is compared with that using o-hydroxyhydroquinonephthalein (Qnph). It is simple, rapid and sensitive, without need for heating or solvent extraction, and the apparent molar absorptivity () is 5.0 x 10(4) 1.mole(-1).cm(-1) at 545 nm; for the Qnph method is 2.8 x 10(4) 1.mole(-1).cm(-1) at 520 nm. Tests with an artificial wastewater gave 99-103% recovery. PMID:18965153

  20. Monitoring of temperature fatigue failure mechanism for polyvinyl alcohol fiber concrete using acoustic emission sensors.

    PubMed

    Li, Dongsheng; Cao, Hai

    2012-01-01

    The applicability of acoustic emission (AE) techniques to monitor the mechanism of evolution of polyvinyl alcohol (PVA) fiber concrete damage under temperature fatigue loading is investigated. Using the temperature fatigue test, real-time AE monitoring data of PVA fiber concrete is achieved. Based on the AE signal characteristics of the whole test process and comparison of AE signals of PVA fiber concretes with different fiber contents, the damage evolution process of PVA fiber concrete is analyzed. Finally, a qualitative evaluation of the damage degree is obtained using the kurtosis index and b-value of AE characteristic parameters. The results obtained using both methods are discussed. PMID:23012555

  1. Composition dependent structural modulations in transparent poly(vinyl alcohol) hydrogels.

    PubMed

    Gupta, Siddhi; Pramanik, Ashit Kumar; Kailath, Ansu; Mishra, Trilochan; Guha, Avijit; Nayar, Suprabha; Sinha, Arvind

    2009-11-01

    Transparent and stable Poly(vinyl alcohol) hydrogels were synthesized from polymer aqueous solution without resorting to a mixed solvent such as dimethyl sulfoxide and water. Contrary to the reported methods involving hydrogen bond induced physical crosslinking by repeated freeze-thawing at -20 degrees C, the present process demonstrates the gelation taking place at relatively higher temperature, i.e. 0 degrees C. While maintaining transparency in all the synthesized hydrogels, the present paper reports systematic structural and morphological variations in the hydrogels as a function of polymer concentration. PMID:19700267

  2. Impact behaviour of an innovative plasticized poly(vinyl chloride) for the automotive industry

    NASA Astrophysics Data System (ADS)

    Bernard, C. A.; Bahlouli, N.; Wagner-Kocher, C.; Ahzi, S.; Rémond, Y.

    2015-09-01

    Plasticized poly(vinyl chloride) (PPVC) is widely used in the automotive industry in the design of structural parts for crashworthiness applications. Thus, it is necessary to study and understand the influence of the mechanical response and mechanical properties of PPVC over a wide range of strain rate, from quasi-static to dynamic loadings. The process is also investigated using different sample thicknesses. In this work, the strain rate effect of a new PPVC is investigated over a wide range of strain rates at three temperatures and for three thicknesses. A modelling of the yield stress is also proposed. The numerical prediction is in good agreement with the experimental results.

  3. Monitoring of Temperature Fatigue Failure Mechanism for Polyvinyl Alcohol Fiber Concrete Using Acoustic Emission Sensors

    PubMed Central

    Li, Dongsheng; Cao, Hai

    2012-01-01

    The applicability of acoustic emission (AE) techniques to monitor the mechanism of evolution of polyvinyl alcohol (PVA) fiber concrete damage under temperature fatigue loading is investigated. Using the temperature fatigue test, real-time AE monitoring data of PVA fiber concrete is achieved. Based on the AE signal characteristics of the whole test process and comparison of AE signals of PVA fiber concretes with different fiber contents, the damage evolution process of PVA fiber concrete is analyzed. Finally, a qualitative evaluation of the damage degree is obtained using the kurtosis index and b-value of AE characteristic parameters. The results obtained using both methods are discussed. PMID:23012555

  4. Sliding of poly(vinyl chloride) on metals studied by Auger electron spectroscopy

    NASA Technical Reports Server (NTRS)

    Pepper, S. V.

    1974-01-01

    The sliding of polyvinyl chloride on nickel, iron and S-Monel has been studied by Auger electron spectroscopy. Polymer was not transferred to the metals, rather shear appeared to take place at the interface. The metal was progressively chlorinated as the polymer made multiple passes on the surface. The thickness of this chlorine film was the order of one atomic layer. Electron-induced desorption studies indicate that the chlorine is chemisorbed to the metal. These results are interpreted as evidence for mechanically induced and/or thermal degradation of the polymer during sliding. Degradation products of HCl and Cl2 which chemisorb to the metal are evolved near the interface.

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

    PubMed

    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. PMID:26428121

  6. 21 CFR 522.960b - Flumethasone acetate solution.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS § 522.960b Flumethasone acetate solution. (a) Specifications....

  7. 21 CFR 522.960b - Flumethasone acetate injection.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...per cubic centimeter: 2 milligrams of flumethasone acetate; 20 milligrams of propylene glycol; 9 milligrams of benzyl alcohol...preservative); 8 milligrams of sodium chloride; 1 milligram of polysorbate 80; 0.1 milligram of citric acid; water for injection...

  8. 21 CFR 522.960b - Flumethasone acetate injection.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...per cubic centimeter: 2 milligrams of flumethasone acetate; 20 milligrams of propylene glycol; 9 milligrams of benzyl alcohol...preservative); 8 milligrams of sodium chloride; 1 milligram of polysorbate 80; 0.1 milligram of citric acid; water for injection...

  9. 21 CFR 522.960b - Flumethasone acetate injection.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...per cubic centimeter: 2 milligrams of flumethasone acetate; 20 milligrams of propylene glycol; 9 milligrams of benzyl alcohol...preservative); 8 milligrams of sodium chloride; 1 milligram of polysorbate 80; 0.1 milligram of citric acid; water for injection...

  10. 21 CFR 522.960b - Flumethasone acetate injection.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...per cubic centimeter: 2 milligrams of flumethasone acetate; 20 milligrams of propylene glycol; 9 milligrams of benzyl alcohol...preservative); 8 milligrams of sodium chloride; 1 milligram of polysorbate 80; 0.1 milligram of citric acid; water for injection...

  11. SOLVENT EXTRACTION OF WASTEWATERS FROM ACETIC-ACID MANUFACTURE

    EPA Science Inventory

    Solvent extraction was evaluated as a potential treatment method for wastewaters generated during the manufacture of acetic acid. Possible goals for an extraction process were considered. For the wastewater samples studied, extraction appeared to be too expensive to be practical ...

  12. Fragrance material review on 2-hydroxy-2-phenylethyl acetate.

    PubMed

    McGinty, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of 2-hydroxy-2-phenylethyl acetate when used as a fragrance ingredient is presented. 2-Hydroxy-2-phenylethyl acetate is a member of the fragrance structural group aryl alkyl alcohol simple acid esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for 2-hydroxy-2-phenylethyl acetate was evaluated then summarized and includes physical properties data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22414656

  13. Fragrance material review on 2-(p-tolyloxy)ethyl acetate.

    PubMed

    McGinty, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of 2-(p-tolyloxy)ethyl acetate when used as a fragrance ingredient is presented. 2-(p-tolyloxy)ethyl acetate is a member of the fragrance structural group aryl alkyl alcohol simple acid esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for 2-(p-tolyloxy)ethyl acetate were evaluated, then summarized, and includes physical properties data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22414652

  14. Degradation by acetic acid for crystalline Si photovoltaic modules

    NASA Astrophysics Data System (ADS)

    Masuda, Atsushi; Uchiyama, Naomi; Hara, Yukiko

    2015-04-01

    The degradation of crystalline Si photovoltaic modules during damp-heat test was studied using some test modules with and without polymer film insertion by observing electrical and electroluminescence properties and by chemical analyses. Acetic acid generated by the hydrolysis decomposition of ethylene vinyl acetate used as an encapsulant is the main origin of degradation. The change in electroluminescence images is explained on the basis of the corrosion of electrodes by acetic acid. On the other hand, little change was observed at the pn junction even after damp-heat test for a long time. Therefore, carrier generation occurs even after degradation; however, such generated carriers cannot be collected owing to corrosion of electrodes. The guiding principle that module structure and module materials without saving acetic acid into the modules was obtained.

  15. 21 CFR 522.960b - Flumethasone acetate injection.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... centimeter: 2 milligrams of flumethasone acetate; 20 milligrams of propylene glycol; 9 milligrams of benzyl alcohol (as preservative); 8 milligrams of sodium chloride; 1 milligram of polysorbate 80; 0.1...

  16. 21 CFR 522.960b - Flumethasone acetate injection.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... centimeter: 2 milligrams of flumethasone acetate; 20 milligrams of propylene glycol; 9 milligrams of benzyl alcohol (as preservative); 8 milligrams of sodium chloride; 1 milligram of polysorbate 80; 0.1...

  17. 21 CFR 522.960b - Flumethasone acetate injection.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... centimeter: 2 milligrams of flumethasone acetate; 20 milligrams of propylene glycol; 9 milligrams of benzyl alcohol (as preservative); 8 milligrams of sodium chloride; 1 milligram of polysorbate 80; 0.1...

  18. 21 CFR 522.960b - Flumethasone acetate injection.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... centimeter: 2 milligrams of flumethasone acetate; 20 milligrams of propylene glycol; 9 milligrams of benzyl alcohol (as preservative); 8 milligrams of sodium chloride; 1 milligram of polysorbate 80; 0.1...

  19. Highly Enantioselective Hydrogenation of Enol Acetates Catalyzed by

    E-print Network

    Zhang, Xumu

    enol acetates. Catalytic asymmetric synthesis presents one of most powerful methods for accessing Although atropisomeric biaryl diphosphines such as BI- NAP,1,4 BIPHEMP,1,5 and MeO-BIPHEP1,5 have been used

  20. Electronic interactions between gold films and mn12-acetate 

    E-print Network

    Means, Joel Lewis

    2009-05-15

    Interactions between Mn12–acetate molecular magnets and thin gold films have been explored in light of the theory of weak localization. Low-temperature measurements of the magnetoresistance of gold films of varying thicknesses, with and without...

  1. 21 CFR 584.200 - Ethyl alcohol containing ethyl acetate.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...gallons of 100 percent ethyl acetate. It is used in accordance with good feeding practices in ruminant feed supplements as a source of added energy. [46 FR 52333, Oct. 27, 1981, as amended at 72 FR 41620, July 31,...

  2. Microorganisms having enhanced resistance to acetate and methods of use

    DOEpatents

    Brown, Steven D; Yang, Shihui

    2014-10-21

    The present invention provides isolated or genetically modified strains of microorganisms that display enhanced resistance to acetate as a result of increased expression of a sodium proton antiporter. The present invention also provides methods for producing such microbial strains, as well as related promoter sequences and expression vectors. Further, the present invention provides methods of producing alcohol from biomass materials by using microorganisms with enhanced resistance to acetate.

  3. Rhodium(iii)-catalyzed C-C coupling of 7-azaindoles with vinyl acetates and allyl acetates.

    PubMed

    Li, Shuai-Shuai; Wang, Cheng-Qi; Lin, Hui; Zhang, Xiao-Mei; Dong, Lin

    2016-01-01

    The behaviour of electron-rich alkenes with 7-azaindoles in rhodium(iii)-catalyzed C-H activation is investigated. Various substituted vinyl acetates and allyl acetates as coupling partners reacted smoothly providing a wide variety of 7-azaindole derivatives, and the selectivity of the coupling reaction is alkene-dependent. In addition, the approaches of rhodium(iii)-catalyzed dehydrogenative Heck-type reaction (DHR) and carbonylation reaction were quite novel and simple. PMID:26553424

  4. Influence of Glyoxal on Preparation of Poly(Vinyl Alcohol)/Poly(Acrylic Acid) Blend Film.

    PubMed

    Park, Ju-Young; Hwang, Kyung-Jun; Yoon, Soon-Do; Lee, Ju-Heon; Lee, In-Hwa

    2015-08-01

    The preparation of a poly(vinyl alcohol)/poly(acrylic acid)/glyoxal film (PVA = poly(vinyl alcohol); PAA = poly(acrylic acid)) with high tensile strength and hydrophobic properties by using the crosslinking reaction for OH group removal is reported herein. PAA was selected as a crosslinking agent because the functional carboxyl group in each monomer unit facilitates reaction with PVA. The OH groups on unreacted PVA were removed by the addition of glyoxal to the PVA/PAA solution. The chemical properties of the PVA/PAA films were investigated using Fourier transformation infrared spectroscopy and the thermal properties of the PVA/PAA/glyoxal films were investigated by means of differential scanning calorimetry and thermogravimetric analysis. A tensile strength of 48.6 N/mm2 was achieved at a PVA/PAA ratio of 85/15 for the PVA/PAA film. The tensile strength of the cross-linked PVA/PAA/glyoxal film (10 wt% glyoxal) was increased by 55% relative to the pure PVA/PAA (85/15) film. The degree of swelling (DS) and solubility (S) of the 10 wt% (PVA/PAA = 85/15, wt%) film added 10 wt% glyoxal were 1.54 and 0.6, respectively. PMID:26369179

  5. Properties of novel polyvinyl alcohol/cellulose nanocrystals/silver nanoparticles blend membranes.

    PubMed

    Xu, Xu; Yang, Yi-Qin; Xing, Ying-Ying; Yang, Jiu-Fang; Wang, Shi-Fa

    2013-11-01

    Novel polyvinyl alcohol (PVA) blend membranes containing cellulose nanocrystals (CNs) and silver nanoparticles (AgNPs) were prepared via a simple method. CNs were prepared by sulfuric acid treatment of microcrystalline cellulose. AgNO3 aqueous solution mixed with the CNs aqueous suspension and was reduced by NaBH4 at room temperature. Purified CNs/AgNPs nanocomposites as functional fillers mixed with polyvinyl alcohol to prepare blend membrane. The morphology, mechanical properties, and antibacterial activities of PVA/CNs/AgNPs composite films were investigated. The PVA/CNs/AgNPs composite films were stable and homogeneous. The tensile strength of PVA was increased from 57.02 MPa to 81.21 MPa when filled with CNs/AgNPs. Antibacterial ratio of PVA/CNs/AgNPs composite against Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus was 96.9% and 88.2%, respectively. The CNs/AgNPs nanocomposites could be applied as bi-functional nanofillers within PVA to improve the mechanical properties and antibacterial activities. PMID:24053842

  6. Acute health effects among firefighters exposed to a polyvinyl chloride (PVC) fire

    SciTech Connect

    Markowitz, J.S.; Gutterman, E.M. ); Schwartz, S.; Link, B.; Gorman, S.M. )

    1989-05-01

    Firefighters are frequently being called on to fight fires that are chemical in nature. In the aftermath of a chemical fire in Plainfield, New Jersey on March 20-21, 1985, the authors conducted a retrospective cohort study which surveyed 80 firefighters exposed to burning polyvinyl chloride (PVC) as well as 15 nonexposed firefighter subjects. By means of an 81-item symptom checklist, exposed firefighters reported more frequent and severe symptoms at 5-6 weeks post incident. This was true for a total symptomatology score as well as 19 individual items. Some of the items with an elevated risk were consistent with exposure to hydrogen chloride, the main pyrolysis product of polyvinyl chloride. Other items with an elevated risk appeared to be related to smoke inhalation while others seemed psychosocial in nature. Analyses conducted within the exposed firefighter group showed that fighting the fire the first day, being a truckman, and residence within 1 mile (1.6 km) of the firehouse were significant risk factors for high total symptom scores. These risk factors may have been associated with level or duration of exposure to the toxic substances produced during the fire.

  7. Rheological and Performance Research on a Regenerable Polyvinyl Alcohol Fracturing Fluid

    PubMed Central

    Shang, Xiaosen; Ding, Yunhong; Wang, Yonghui; Yang, Lifeng

    2015-01-01

    A regenerable polyvinyl alcohol/organic boron fracturing fluid system with 1.6 wt% polyvinyl alcohol (PVOH) and 1.2 wt% organic boron (OBT) was studied, and its main regeneration mechanism is the reversible cross-linking reaction between B(OH)4- and hydroxyl groups of PVOH as the change of pH. Results of rheology evaluations show that both the apparent viscosity and the thermal stability of the fracturing fluid decreased with the regeneration number of times increasing. In addition, the apparent viscosity of the fluid which was without regeneration was more sensitive to the shear action compared with that of the fluid with regeneration once or twice. When the fracturing fluid was without regeneration, the elasticity was dominating due to the three-dimensional network structure of the formed gel; the viscosity gradually occupied the advantage when the fracturing fluid was regenerated once or twice. The settling velocity of proppant was accelerated by both the regeneration process and the increasing temperature, but it was decelerated when the proppant ratio increased. Results of core damage tests indicate that less permeability damage was caused by the PVOH/OBT fracturing fluid compared with that caused by the guar gum fracturing fluid after gel breaking. PMID:26641857

  8. 21 CFR 862.1390 - 5-Hydroxyindole acetic acid/serotonin test system.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false 5-Hydroxyindole acetic acid/serotonin test system... Test Systems § 862.1390 5-Hydroxyindole acetic acid/serotonin test system. (a) Identification. A 5-hydroxyindole acetic acid/serotonin test system is a device intended to measure 5-hydroxyindole acetic...

  9. 21 CFR 862.1390 - 5-Hydroxyindole acetic acid/serotonin test system.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 8 2012-04-01 2012-04-01 false 5-Hydroxyindole acetic acid/serotonin test system... Test Systems § 862.1390 5-Hydroxyindole acetic acid/serotonin test system. (a) Identification. A 5-hydroxyindole acetic acid/serotonin test system is a device intended to measure 5-hydroxyindole acetic...

  10. 21 CFR 862.1390 - 5-Hydroxyindole acetic acid/serotonin test system.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false 5-Hydroxyindole acetic acid/serotonin test system... Test Systems § 862.1390 5-Hydroxyindole acetic acid/serotonin test system. (a) Identification. A 5-hydroxyindole acetic acid/serotonin test system is a device intended to measure 5-hydroxyindole acetic...

  11. 21 CFR 862.1390 - 5-Hydroxyindole acetic acid/serotonin test system.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 8 2013-04-01 2013-04-01 false 5-Hydroxyindole acetic acid/serotonin test system... Test Systems § 862.1390 5-Hydroxyindole acetic acid/serotonin test system. (a) Identification. A 5-hydroxyindole acetic acid/serotonin test system is a device intended to measure 5-hydroxyindole acetic...

  12. 21 CFR 862.1390 - 5-Hydroxyindole acetic acid/serotonin test system.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false 5-Hydroxyindole acetic acid/serotonin test system... Test Systems § 862.1390 5-Hydroxyindole acetic acid/serotonin test system. (a) Identification. A 5-hydroxyindole acetic acid/serotonin test system is a device intended to measure 5-hydroxyindole acetic...

  13. Laboratory millimeter wave spectrum and astronomical search for vinyl acetate

    NASA Astrophysics Data System (ADS)

    Kolesniková, L.; Peña, I.; Alonso, J. L.; Cernicharo, J.; Tercero, B.; Kleiner, I.

    2015-05-01

    Context. The recent discovery of methyl acetate in Orion KL makes vinyl acetate, CH3C=OOCH=CH2, a potential molecule in the interstellar medium. We obtained very accurate spectroscopic constants in a comprehensive laboratory analysis of its rotational spectra which can be used to predict those transition frequencies towards interstellar sources. Aims: We present the experimental study and theoretical analysis of the ground torsional state of vinyl acetate in a large spectral range for astrophysical use. Methods: The room-temperature rotational spectrum of vinyl acetate has been measured from 125 to 305 GHz to provide direct frequencies to the astronomical community. Additional measurements have also been made using a broadband CP-FTMW spectrometer in the region of 6-18 GHz. Transition lines, corresponding to the most stable conformer, have been observed and assigned. All the rotational transitions revealed the A-E splitting due to the methyl internal rotation and had to be treated with a specific internal rotation code (BELGI-Cs). Results: We analyzed 2508 transitions up to J'' = 75 for vt = 0 for the most stable conformer of vinyl acetate. The new lines were globally fitted with previously published data and 24 parameters of the Hamiltonian were accurately determined. The spectral features of vinyl acetate were then searched for in Orion KL. Using the whole line survey of Orion KL (80-280 GHz) obtained with the IRAM 30 m radio telescope we can provide only an upper limit to the column density of vinyl acetate. However, using the ALMA science verification data we obtain a tentative detection of this species that will require further search at other frequencies to confirm its presence in this high mass star forming region. Table 2 is only available at the CDS via anonymous ftp to http://cdsarc.u-strasbg.fr (ftp://130.79.128.5) or via http://cdsarc.u-strasbg.fr/viz-bin/qcat?J/A+A/577/A91

  14. Tetrazole acetic acid: Tautomers, conformers, and isomerization

    SciTech Connect

    Araujo-Andrade, C.; Department of Chemistry, University of Coimbra, 3004-535 Coimbra ; Reva, I. Fausto, R.

    2014-02-14

    Monomers of (tetrazol-5-yl)-acetic acid (TAA) were obtained by sublimation of the crystalline compound and the resulting vapors were isolated in cryogenic nitrogen matrices at 13 K. The conformational and tautomeric composition of TAA in the matrix was characterized by infrared spectroscopy and vibrational calculations carried out at the B3LYP/6-311++G(d,p) level. TAA may adopt two tautomeric modifications, 1H- and 2H-, depending on the position of the annular hydrogen atom. Two-dimensional potential energy surfaces (PESs) of TAA were theoretically calculated at the MP2/6-311++G(d,p) level, for each tautomer. Four and six symmetry-unique minima were located on these PESs, for 1H- and 2H-TAA, respectively. The energetics of the detected minima was subsequently refined by calculations at the QCISD level. Two 1H- and three 2H-conformers fall within the 0–8 kJ mol{sup ?1} energy range and should be appreciably populated at the sublimation temperature (?330 K). Observation of only one conformer for each tautomer (1ccc and 2pcc) is explained in terms of calculated barriers to conformational rearrangements. All conformers with the cis O=COH moiety are separated by low barriers (less than 10 kJ mol{sup ?1}) and collapse to the most stable 1ccc (1H-) and 2pcc (2H-) forms during deposition of the matrix. On the trans O=COH surfaces, the relative energies are very high (between 12 and 27 kJ mol{sup ?1}). The trans forms are not thermally populated at the sublimation conditions and were not detected in matrices. One high-energy form in each tautomer, 1cct (1H-) and 2pct (2H-), was found to differ from the most stable form only by rotation of the OH group and separated from other forms by high barriers. This opened a perspective for their stabilization in a matrix. 1cct and 2pct were generated in the matrices selectively by means of narrow-band near-infrared (NIR) irradiations of the samples at 6920 and 6937 cm{sup ?1}, where the first OH stretching overtone vibrations of 1ccc and 2pcc occur. The reverse transformations could be induced by irradiations at 7010 and 7030 cm{sup ?1}, transforming 1cct and 2pct back to 1ccc and 2pcc, also selectively. Besides the NIR-induced transformations, the photogenerated 1cct and 2pct forms also decay in N{sub 2} matrices back to 1ccc and 2pcc spontaneously, with characteristic decay times of hours (1H) and tens of minutes (2H). The decay mechanism is rationalized in terms of the proton tunneling. In crystals, TAA exists exclusively as 1H-tautomer. By contrast, the tautomeric composition of the matrix-isolated monomers was found to consist of both 1H- and 2H-tautomers, in comparable amounts. A mechanistic discussion of the tautomerization process occurring during sublimation, accounting also for the observed minor decomposition of TAA leading to CO{sub 2} and 5-methyl-tetrazole, is proposed.

  15. Zuclopenthixol acetate for acute schizophrenia and similar serious mental illnesses

    PubMed Central

    Jayakody, Kaushadh; Gibson, Roger Carl; Kumar, Ajit; Gunadasa, Shalmini

    2014-01-01

    Background Medication used for acute aggression in psychiatry must have rapid onset of effect, low frequency of administration and low levels of adverse effects. Zuclopenthixol acetate is said to have these properties. Objectives To estimate the clinical effects of zuclopenthixol acetate for the management of acute aggression or violence thought to be due to serious mental illnesses, in comparison to other drugs used to treat similar conditions. Search methods We searched the Cochrane Schizophrenia’s Group Trials Register (July 2011). We supplemented this by citation searching and personal contact with authors and relevant pharmaceutical companies. Selection criteria All randomised clinical trials involving people thought to have serious mental illnesses comparing zuclopenthixol acetate with other drugs. Data collection and analysis Two review authors extracted and cross-checked data independently. We calculated fixed-effect relative risks (RR) and 95% confidence intervals (CI) for dichotomous data. We analysed by intention-to-treat. We used mean differences (MD) for continuous variables. Main results We found no data for the primary outcome, tranquillisation. Compared with haloperidol, zuclopenthixol acetate was no more sedating at two hours (n = 40, 1 RCT, RR 0.60, 95% CI 0.27 to 1.34). People given zuclopenthixol acetate were not at reduced risk of being given supplementary antipsychotics (n = 134, 3 RCTs, RR 1.49, 95% CI 0.97 to 2.30) although additional use of benzodiazepines was less (n = 50, 1 RCT, RR 0.03, 95% CI 0.00 to 0.47). People given zuclopenthixol acetate had fewer injections over seven days compared with those allocated to haloperidol IM (n = 70, 1 RCT, RR 0.39, 95% CI 0.18 to 0.84, NNT 4, CI 3 to 14). We found no data on more episodes of aggression or harm to self or others. One trial (n = 148) reported no significant difference in adverse effects for people receiving zuclopenthixol acetate compared with those allocated haloperidol at one, three and six days (RR 0.74, 95% CI 0.43 to 1.27). Compared with haloperidol or clotiapine, people allocated zuclopenthixol did not seem to be at more risk of a range of movement disorders (< 20%). Three studies found no difference in the proportion of people getting blurred vision/dry mouth (n = 192, 2 RCTs, RR at 24 hours 0.90, 95% CI 0.48 to 1.70). Similarly, dizziness was equally infrequent for those allocated zuclopenthixol acetate compared with haloperidol (n = 192, 2 RCTs, RR at 24 hours 1.15, 95% CI 0.46 to 2.88). There was no difference between treatments for leaving the study before completion (n = 522, RR 0.85, 95% CI 0.31 to 2.31). One study reported no difference in adverse effects and outcome scores, when high dose (50-100 mg/injection) zuclopenthixol acetate was compared with low dose (25-50 mg/injection) zuclopenthixol acetate. Authors’ conclusions Recommendations on the use of zuclopenthixol acetate for the management of psychiatric emergencies in preference to ‘standard’ treatment have to be viewed with caution. Most of the small trials present important methodological flaws and findings are poorly reported. This review did not find any suggestion that zuclopenthixol acetate is more or less effective in controlling aggressive acute psychosis, or in preventing adverse effects than intramuscular haloperidol, and neither seemed to have a rapid onset of action. Use of zuclopenthixol acetate may result in less numerous coercive injections and low doses of the drug may be as effective as higher doses. Well-conducted pragmatic randomised controlled trials are needed. PMID:22513898

  16. VALIDATION OF AN EPA METHOD FOR THE ION CHROMATOGRAPHIC DETERMINATION OF PERCHLORATE IN FERTILIZERS USING A POLYVINYL ALCOHOL GEL RESIN.

    EPA Science Inventory

    This paper summarizes the key points of a joint study between the EPA and Metrohm-Peak, Inc., on the use of polyvinyl alcohol [PVA] columns for the ion chromatographic determination of percholorate in aqueous leachates or solutions of fertilizers. A series of fertilizer samples ...

  17. Thermally stimulated transformation of the structure of cobalt complexes in polyvinyl alcohol-cobalt(II) chloride systems

    NASA Astrophysics Data System (ADS)

    Stukalova, A. S.; Prosanov, I. Yu.

    2007-11-01

    We present the kinetic and temperature dependences of the optical absorption of thermochromic films of polyvinyl alcohol with added CoCl2. Based on the data obtained, we have analyzed the possibility that tetrahedral cobalt complexes are formed from octahedral complexes.

  18. A novel biobased plasticizer of epoxidized cardanol glycidylether: Synthesis and application in soft poly(vinyl chloride) films

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A novel plasticizer derived from cardanol, epoxied cardanol glycidyl ether (ECGE), was synthesized and characterized by 1H-NMR and 13C-NMR. Effects of the ECGE combined with dioctyl phthalate (DOP), a commercial plasticizer, in soft poly(vinyl chloride) (PVC) films were studied. Dynamic mechanical a...

  19. Adiabatic calorimetry (RSST and VSP) tests with sodium acetate

    SciTech Connect

    Kirch, N.W.

    1993-09-01

    As requested in the subject reference, adiabatic calorimetry (RSST and VSP) tests have been performed with sodium acetate covering TOC concentrations from 3 to 7% with the following results: Exothermic activity noted around 200{degrees}C. Propagating reaction initiated at about 300{degrees}C. Required TOC concentration for propagation estimated at about 6 w% (dry mixture) or about 20 w% sodium acetate. Heat of reaction estimated to be 3.7 MJ per kg of sodium acetate (based on VSP test with 3 w% TOC and using a dry mixture specific heat of 1000 J kg{sup {minus}1} K{sup {minus}1}). Based upon the above results we estimate that a moisture content in excess of 14 w% would prevent a propagating reaction of a stoichiometric mixture of fuel and oxidizer ({approximately} 38 w% sodium acetate and {approximately}62 w% sodium nitrate). Assuming that the fuel can be treated as sodium acetate equivalent, and considering that the moisture content in the organic containing waste generally is believed to be in excess of 14 w%, it follows that the possibility of propagating reactions in the Hanford waste tanks can be ruled out.

  20. Effects of physical properties for starch acetate powders on tableting.

    PubMed

    Korhonen, Ossi; Pohja, Seppo; Peltonen, Soili; Suihko, Eero; Vidgren, Mika; Paronen, Petteri; Ketolainen, Jarkko

    2002-01-01

    The aim of the study was to investigate particle and powder properties of various starch acetate powders, to study the effect of these properties on direct compression characteristics, and to evaluate the modification opportunity of physical properties for starch acetate powders by using various drying methods. At the end of the production phase of starch acetate, the slurry of starch acetate was dried using various techniques. Particle, powder, and tableting properties of end products were investigated. Particle size, circularity, surface texture, water content and specific surface area varied according to the particular drying method of choice. However, all powders were freely flowing. Bulk and tapped densities of powders varied in the range of 0.29 to 0.44 g/cm3 and 0.39 to 0.56 g/cm3, respectively. Compaction characteristics revealed that all powders were easily deformed under compression, having yield pressure values of less than 66 MPa according to Heckel analysis. All powders possessed a significant interparticulate bond-forming capacity during compaction. The tensile strength values of tablets varied between 10 and 18 MPa. In conclusion, physical properties of starch acetate could be affected by various drying techniques. A large specific surface area and water content above 4% were favorable properties by direct compression, especially for small, irregular, and rough particles. PMID:12916928

  1. Growth of Chlamydomonas reinhardtii in acetate-free medium when co-cultured with alginate-encapsulated, acetate-producing strains of Synechococcus sp. PCC 7002

    DOE PAGESBeta

    Therien, Jesse B.; Zadvornyy, Oleg A.; Posewitz, Matthew C.; Bryant, Donald A.; Peters, John W.

    2014-10-18

    The model alga Chlamydomonas reinhardtii requires acetate as a co-substrate for optimal production of lipids, and the addition of acetate to culture media has practical and economic implications for algal biofuel production. We demonstrate the growth of C. reinhardtii on acetate provided by mutant strains of the cyanobacterium Synechococcus sp. PCC7002.

  2. [Conversion of acetic acid to methane by thermophiles

    SciTech Connect

    Zinder, S.H.

    1993-01-01

    The primary goal of this project is to obtain a better understanding of thermophilic microorganisms which convert acetic acid to CH[sub 4]. The previous funding period represents a departure from earlier research in this laboratory, which was more physiological and ecological. The present work is centered on the biochemistry of the thermophile Methanothrix sp. strain CALS-1. this organism presents a unique opportunity, with its purity and relatively rapid growth, to do comparative biochemical studies with the other major acetotrophic genus Methanosarcina. We previously found that Methanothrix is capable of using acetate at concentrations 100 fold lower than Methanosarcina. This finding suggests that there are significant differences in the pathways of methanogenesis from acetate in the two genera.

  3. Acetate Metabolism in Anaerobes from the Domain Archaea

    PubMed Central

    Ferry, James G.

    2015-01-01

    Acetate and acetyl-CoA play fundamental roles in all of biology, including anaerobic prokaryotes from the domains Bacteria and Archaea, which compose an estimated quarter of all living protoplasm in Earth’s biosphere. Anaerobes from the domain Archaea contribute to the global carbon cycle by metabolizing acetate as a growth substrate or product. They are components of anaerobic microbial food chains converting complex organic matter to methane, and many fix CO2 into cell material via synthesis of acetyl-CoA. They are found in a diversity of ecological habitats ranging from the digestive tracts of insects to deep-sea hydrothermal vents, and synthesize a plethora of novel enzymes with biotechnological potential. Ecological investigations suggest that still more acetate-metabolizing species with novel properties await discovery. PMID:26068860

  4. Isothermal decomposition of gamma-irradiated palladium acetate

    NASA Astrophysics Data System (ADS)

    Mahfouz, R. M.; Alshehri, S. M.; Monshi, M. A. S.; Abd El-Salam, N. M.

    2004-06-01

    The isothermal decomposition of un-irradiated (pristine) and pre-gamma-irradiated palladium acetate was studied in the temperature range (498-508 K) and in air using the isothermal thermogravimetric technique. The data were analysed using various solid state reaction models. The results showed that the kinetics of isothermal decomposition of palladium acetate was governed by random nucleation reaction (Erofe'ev equation A(3)). The activation energies of the main decomposition process for un-irradiated and pre-gamma-irradiated samples were calculated. The change in texture and crystal structure of the investigated palladium acetate by gamma-irradiation was studied using electron microscopy and X-ray diffraction techniques.

  5. Disinfection of mung bean seed with gaseous acetic acid.

    PubMed

    Delaquis, P J; Sholberg, P L; Stanich, K

    1999-08-01

    Mung bean seed inoculated with Salmonella Typhimurium, Escherichia coli O157:H7, and Listeria monocytogenes (3 to 5 log CFU/g) was exposed to gaseous acetic acid in an aluminum fumigation chamber. Salmonella Typhimurium and E. coli O157:H7 were not detected by enrichment of seeds treated with 242 microl of acetic acid per liter of air for 12 h at 45 degrees C. L. monocytogenes was recovered by enrichment from two of 10 25-g seed samples treated in this manner. Fumigation with gaseous acetic acid was also lethal to indigenous bacteria and fungi on mung bean seed. The treatment did not significantly reduce seed germination rates, and no differences in surface microstructure were observed between treated and untreated seed viewed by scanning electron microscopy. PMID:10456753

  6. Acetate Metabolism in Anaerobes from the Domain Archaea.

    PubMed

    Ferry, James G

    2015-01-01

    Acetate and acetyl-CoA play fundamental roles in all of biology, including anaerobic prokaryotes from the domains Bacteria and Archaea, which compose an estimated quarter of all living protoplasm in Earth's biosphere. Anaerobes from the domain Archaea contribute to the global carbon cycle by metabolizing acetate as a growth substrate or product. They are components of anaerobic microbial food chains converting complex organic matter to methane, and many fix CO2 into cell material via synthesis of acetyl-CoA. They are found in a diversity of ecological habitats ranging from the digestive tracts of insects to deep-sea hydrothermal vents, and synthesize a plethora of novel enzymes with biotechnological potential. Ecological investigations suggest that still more acetate-metabolizing species with novel properties await discovery. PMID:26068860

  7. N-Type Thermoelectric Performance of Functionalized Carbon Nanotube-Filled Polymer Composites

    PubMed Central

    Freeman, Dallas D.; Choi, Kyungwho; Yu, Choongho

    2012-01-01

    Carbon nanotubes (CNTs) were functionalized with polyethyleneimine (PEI) and made into composites with polyvinyl acetate (PVAc). CNTs were dispersed with different amounts of sodium dodecylbenzenesulfonate (SDBS) prior to the PEI functionalization. The resulting samples exhibit air-stable n-type characteristics with electrical conductivities as great as 1500 S/m and thermopowers as large as ?100 µV/K. Electrical conductivity and thermopower were strongly affected by CNT dispersion, improving the properties with better dispersion with high concentrations of SDBS. This improvement is believed to be due to the increase in the number of tubes that are evenly coated with PEI in a better-dispersed sample. Increasing the amount of PEI relative to the other constituents positively affects thermopower but not conductivity. Air exposure reduces both thermopower and conductivity presumably due to oxygen doping (which makes CNTs p-type), but stable values were reached within seven days following sample fabrication. PMID:23133605

  8. Water transport in cement-in-polymer dispersions at variable temperature studied by magnetic resonance imaging

    SciTech Connect

    Olaru, A.M. Bluemich, B.; Adams, A.

    2013-02-15

    The hydration of recently developed cement-in-polymer dispersions (c/p) containing 30% and 40% poly (vinyl acetate) [PVAc] and 30% poly(vinyl alcohol) [PVA] was monitored on-line at various temperatures using {sup 1}H Single Point Imaging (SPI). The physical changes undergone by the materials as well as the complex manner in which the absorption process takes place and the evolution of the spin density were characterized and were found to be strongly dependent on the nature and amount of polymer and on the temperature. Based on the results obtained we propose a simple mathematical model which can be used to characterize the behaviour of the c/p dispersions exposed to hydration at variable temperature.

  9. Fabrication and characterization of polycrystalline WO3 nanofibers and their application for ammonia sensing

    SciTech Connect

    Wang,G.; Ji, Y.; Huang, X.; Yang, X.; Gouma, P.; Dudley, M.

    2006-01-01

    We describe the fabrication and characterization of tungsten oxide nanofibers using the electrospinning technique and sol-gel chemistry. Tungsten isopropoxide sol-gel precursor was incorporated into poly(vinyl acetate)(PVAc)/DMF solutions and electrospun to form composite nanofibers. The as-spun composite nanofibers were subsequently calcinated to obtain pure tungsten oxide nanofibers with controllable diameters of around 100 nm. SEM and TEM were utilized to investigate the structure and morphology of tungsten oxide nanofibers before and after calcination. The relationship between solution concentration and ceramic nanofiber morphology has been studied. A synchrotron-based in situ XRD method was employed to study the dynamic structure evolution of the tungsten oxide nanofibers during the calcination process. It has been shown that the as-prepared tungsten oxide ceramic nanofibers have a quick response to ammonia with various concentrations, suggesting potential applications of the electrospun tungsten oxide nanofibers as a sensor material for gas detection.

  10. Fabrication and Characterization of Polycrystalline WO3 Nanofibers and Their Application for Ammonia Sensing

    SciTech Connect

    Wang,G.; Ji, Y.; Huang, X.; Yang, X.; Gouma, P.; Dudley, M.

    2006-01-01

    We describe the fabrication and characterization of tungsten oxide nanofibers using the electrospinning technique and sol-gel chemistry. Tungsten isopropoxide sol-gel precursor was incorporated into poly(vinyl acetate)(PVAc)/DMF solutions and electrospun to form composite nanofibers. The as-spun composite nanofibers were subsequently calcinated to obtain pure tungsten oxide nanofibers with controllable diameters of around 100 nm. SEM and TEM were utilized to investigate the structure and morphology of tungsten oxide nanofibers before and after calcination. The relationship between solution concentration and ceramic nanofiber morphology has been studied. A synchrotron-based in situ XRD method was employed to study the dynamic structure evolution of the tungsten oxide nanofibers during the calcination process. It has been shown that the as-prepared tungsten oxide ceramic nanofibers have a quick response to ammonia with various concentrations, suggesting potential applications of the electrospun tungsten oxide nanofibers as a sensor material for gas detection.

  11. Impedance spectroscopy on dye-sensitized solar cells with a poly(ethylenedioxythiophene):poly(styrenesulfonate) counter electrolyte

    NASA Astrophysics Data System (ADS)

    Kim, Young-Keun; Park, Sung-Hae; Hwang, Won-Pill; Seo, Min-Hye; Park, Hyun-Woo; Jang, Young-Wook; Kim, Mi-Ra; Lee, Jin-Kook

    2012-06-01

    We have successfully fabricated the dye-sensitized solar cell (DSSC) devices using ruthenium complex dye, polymer electrolytes, and poly(ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT: PSS) as a counter electrode. The overall power conversion efficiencies of the devices using polyethylene oxide (PEO), polyethylene glycol (PEG), polymethylmethacrylate (PMMA), and polyvinyl acetate (PVAc) as polymer electrolytes were 4.08%, 3.87%, 0.49%, and 0.20%, respectively, while the efficiencies of DSSC devices using Pt counter electrodes showed similar values of 5.7 ± 0.1%. The differences in the efficiencies and the charge transfer resistances (R CT ) of the DSSCs with various polymer electrolytes and counter electrodes were measured by using an electrochemical impedance analyzer (EIS) and are discussed.

  12. Pulmonary and percutaneous absorption of 2-propoxyethyl acetate and 2-ethoxyethyl acetate in beagle dogs

    SciTech Connect

    Guest, D.; Hamilton, M.L.; Deisinger, P.J.; DiVincenzo, G.D.

    1984-08-01

    A comparison was made of the absorption and elimination rates of 2-propoxyethyl acetate (PEA) and 2-ethoxyethyl acetate (EEA) following inhalation, dermal application of IV administration. Male beagle dogs were exposed to 50 ppm PEA or EEA for 5 hr, and breath samples were collected during the exposure and a 3-hr recovery period. Both compounds were rapidly absorbed through the lungs. After 10 min of exposure, the concentrations of the parent compounds in the expired breath were 5 to 10 ppm (80-90% absorption) and reached plateau values at about 3 hr of 13 ppm for PEA (74% absorption) and 16 ppm for EEA (68% absorption). Post-exposure breath samples declined exponentially to 0.5 ppm and 2 ppm after 3 hr for PEA and EEA, respectively. Expired concentrations of PEA were slightly, but significantly (p < 0.025), lower than those of EEA at corresponding times during the exposure. After IV dosing with 1 mg/kg (ethyl-1,2-/sup 14/C)PEA, the urine contained 61% and 88% of the dose in 4 and 24 hr, respectively. (/sup 14/C)EEA was eliminated more slowly, with 20% and 61% of the dose appearing in the urine in 4 and 24 hr, respectively. Blood elimination half-lives were 1.6 hr for (/sup 14/C)PEA and 7.9 hr for (/sup 14/C)EEA. Only trace amounts of /sup 14/CO/sub 2/ (<1%) or volatile materials (<0.1%) were detected in the expired air with either compound. For studies of percutaneous absorption, (/sup 14/C)PEA or (/sup 14/C)EEA was added to undiluted compounds and applied in a glass cell to a shaved area on a dog's thorax for 30 or 60 min. Blood and expired air were collected for 8 hr and urine for 24 hr. The pattern of urinary elimination for each compound was similar to that seen after IV dosing with (/sup 14/C)PEA being excreted more rapidly than (/sup 14/C)EEA. 15 references, 4 figures, 4 tables.

  13. Mass spectra of methyl acetate and ethyl formate

    NASA Astrophysics Data System (ADS)

    Liu, Min; Wu, Chengyin; Wu, Zhifeng; Liang, Qingqing; Deng, Yongkai; Gong, Qihuang; Sun, Yue; Xu, Yuntao; Zhao, Yujie; Shan, Xiaobin; Liu, Fuyi; Sheng, Liusi

    2009-01-01

    We experimentally investigate the ionization and dissociation of two isomers, methyl acetate (CH 3COOCH 3) and ethyl formate (CH 3CH 2COOH), irradiated by strong laser pulses with a pulse duration of 7 fs. Strong parent ions are observed for both isomers. However, main fragmental ions are CH 3CO + and CH3+ for methyl acetate and CH 3O + and CH4+ for ethyl formate. Through comparing with the single photon ionization mass spectra of these two isomers, we find that these fragments are produced by the direct dissociation of the parent ions in different excited electronic states.

  14. Response to aminoglutethimide and cortisone acetate in advanced prostatic cancer.

    PubMed Central

    Ponder, B. A.; Shearer, R. J.; Pocock, R. D.; Miller, J.; Easton, D.; Chilvers, C. E.; Dowsett, M.; Jeffcoate, S. L.

    1984-01-01

    Forty patients with metastatic adenocarcinoma of the prostate were evaluated for response to treatment with aminoglutethimide plus cortisone acetate. All had relapsed from or failed to respond to primary endocrine treatment with orchidectomy or stilboestrol. Nineteen patients (48%) showed subjective response, in most cases relief of bone pain. Side effects limited treatment in only 3 patients. We conclude that aminoglutethimide plus cortisone acetate is a useful addition to the treatment available for this difficult group of patients. The mechanism by which this treatment has a beneficial effect remains unclear. PMID:6238616

  15. Reverse osmosis performance of modified polyvinyl alcohol thin-film composite membranes

    SciTech Connect

    Lang, K.; Chowdhury, G.; Matsuura, T.; Sourirajan, S. )

    1994-08-01

    Membrane separation characteristics in the nanofiltration (NF) and reverse osmosis (RO) regions of the filtration spectrum are governed by a complex combination of both steric hindrance and surface force interactions. NF and RO membranes having surface charges show unusual selectivity behavior not predicted on the basis of physical pore size alone. Hence, practical characterizations should employ techniques to gain insight on membrane function. In this work, the separation characteristics of an anionically charged modified polyvinyl alcohol (PVA) thin-film composite membrane under different operating pressures were investigated. A qualitative measurement of the surface force interactions between solutes and membrane polymer was conducted using liquid chromatography technique. An attempt was also made to study the chlorine resistance of the composite membrane.

  16. Spectroelectrochemical Studies on Quinacridone by Using Poly(vinyl alcohol) Coating as Protection Layer

    PubMed Central

    Enengl, Sandra; Enengl, Christina; Stadler, Philipp; Neugebauer, Helmut; Sariciftci, Niyazi Serdar

    2015-01-01

    Spectroscopic measurements in the infrared range combined with electrochemistry are a powerful technique for investigation of organic semiconductors to track changes during oxidation and reduction (p- and n-doping) processes. For these measurements it is important that the studied material, mostly deposited as a thin film on an internal reflection element, does not dissolve during this characterization. In this study we introduce a technique that allows infrared spectroelectrochemical characterization of films of these materials for the first time. In many cases so far this has been impossible, due to solubility in the oxidized and/or reduced form. This novel technique is shown on thin films of quinacridone by adding a protection layer of poly(vinyl alcohol) (PVA). PMID:26013836

  17. Nanofibrillated Cellulose and Copper Nanoparticles Embedded in Polyvinyl Alcohol Films for Antimicrobial Applications

    PubMed Central

    Zhong, Tuhua; Oporto, Gloria S.; Jaczynski, Jacek; Jiang, Changle

    2015-01-01

    Our long-term goal is to develop a hybrid cellulose-copper nanoparticle material as a functional nanofiller to be incorporated in thermoplastic resins for efficiently improving their antimicrobial properties. In this study, copper nanoparticles were first synthesized through chemical reduction of cupric ions on TEMPO nanofibrillated cellulose (TNFC) template using borohydride as a copper reducing agent. The resulting hybrid material was embedded into a polyvinyl alcohol (PVA) matrix using a solvent casting method. The morphology of TNFC-copper nanoparticles was analyzed by transmission electron microscopy (TEM); spherical copper nanoparticles with average size of 9.2 ± 2.0?nm were determined. Thermogravimetric analysis and antimicrobial performance of the films were evaluated. Slight variations in thermal properties between the nanocomposite films and PVA resin were observed. Antimicrobial analysis demonstrated that one-week exposure of nonpathogenic Escherichia coli DH5? to the nanocomposite films results in up to 5-log microbial reduction. PMID:26137482

  18. Effects of solvent dehydration on creep resistance of poly(vinyl alcohol) hydrogel.

    PubMed

    Choi, Jeeyoung; Bodugoz-Senturk, Hatice; Kung, Hsiang J; Malhi, Arnaz S; Muratoglu, Orhun K

    2007-02-01

    As a synthetic replacement material for osteochondral defect repair, poly(vinyl alcohol) (PVA) hydrogels offer a great potential due to their high water content and strong mechanical integrity. To survive the high stress environment in the joint space, high creep resistance becomes one of the key requirements for hydrogel implants. We hypothesized that reducing the equilibrium water content (EWC) of hydrogels would improve their creep resistance. We investigated the effect of dehydration of PVA theta-gels in various solvent/solution media followed by rehydration in saline solution. Decreasing EWC increased the creep resistance of PVA theta-gels. The most effective medium was isopropyl alcohol for reducing the EWC and increasing the creep resistance of PVA theta-gels. PMID:17070904

  19. Polyvinyl chloride plastics in municipal solid waste combustion. Impact upon dioxin emissions: A synthesis of views

    SciTech Connect

    Not Available

    1993-04-01

    This report examines the issue of whether the polyvinyl chloride (PVC) plastics content of municipal solid waste (MSW) is a significant contributor to emissions of chlorinated dibenzo-p-dioxins (dioxins) that are associated with MSW combustion. Indications based on a consideration of this issue are developed through a synthesis of available information. While there is convincing experimental evidence that various conditions can cause production of dioxins when PVC is thermally treated, a fundamental issue that remains to be solved is how these findings relate to operating conditions that are characteristic of well designed, maintained and operated MSW combustion facilities, equipped with modern air pollution controls. These findings largely have been derived from laboratory or pilot scale experimentation and from full-scale studies that have carried out at facilities of varying design and purpose.

  20. Structure-property relationships in Sterculia urens/polyvinyl alcohol electrospun composite nanofibres.

    PubMed

    Patra, Niranjan; Martinová, Lenka; Stuchlik, Martin; ?erník, Miroslav

    2015-04-20

    Sterculia urens (Gum Karaya) based polyvinyl alcohol (PVA) composite nanofibres have been successfully electrospun after chemical modification of S. urens to increase its solubility. The effect of deacetylated S. urens (DGK) on the morphology, structure, crystallization behaviour and thermal stability was studied for spuned fibres before and after spinning post treatment. An apparent increase in the PVA crystallinity were observed in the PVA-DGK composite nanofibres indicating S. urens induced crystallization of PVA. The pure PVA nanofibre and the nanofibres of PVA-DGK composites were introduced to post electrospinning heat treatment at 150°C for 15 min. The presence of sterculia gum reduced the fibre diameter and distribution of the nanofibres due to the increased stretching of the fibres during spinning. Switching of the thermal behaviour occurs due to post spinning heat treatments. PMID:25662689

  1. Dual fluorescence of N-pyrrolobenzonitrile in extended polyvinyl alcohol films

    NASA Astrophysics Data System (ADS)

    Roznowska, A.; Tomin, V. I.; Fisz, J.; Hubisz, K.

    2011-07-01

    The possibility of radically changing the conditions for charge transfer (CT) photoreaction in N-pyrrolobenzonitrile molecules in polymer matrices of polyvinyl alcohol (PVA) under their extension has been demonstrated. The fluorescence spectrum of N-pyrrolobenzonitrile in PVA has two characteristic bands in the UV and visible spectral ranges, which are indicative of the CT reaction that occurs in the excited state. Extension significantly reduces the intensity of the UV band, the contribution of which in unstrained samples is comparable with the violet fluorescence intensity. Even a single extension of PVA films significantly reduces the intensity of the UV band, while a sixfold extension dramatically enhances this effect. In the latter case, the fluorescence spectrum contains a strong CT band whose relative intensity exceeds that for highly polar aprotic solvent acetonitrile by a factor of five. The data obtained indicate that, using extension, one can change the main intermolecular factors affecting the CT rate in PVA samples.

  2. Thermal Conductivity of Al2O3/Poly(vinyl butyral) Composites

    NASA Astrophysics Data System (ADS)

    Ju, Han Sae; Hyeok Im, Dong; Park, Sung Dae; Lee, Hyeung Gyu; Kim, Eung Soo

    2012-09-01

    In this study, the effects of orientation of Al2O3 on the thermal conductivity of poly(vinyl butyral) (PVB) composites filled with platelet-shaped Al2O3 ceramics were investigated as function of Al2O3 content. On increasing the ceramic content, it was observed that the thermal conductivity of the composites increased because of the higher thermal conductivity of Al2O3 compared with that of the PVB. The thermal conductivity of the composites was affected by the orientation of ceramics. The measured thermal conductivity of the composites was compared with the effective thermal conductivity calculated by various theoretical models. The thermal diffusivity and specific heat capacity of the composites were also discussed.

  3. Complete Genome Sequence of Polyvinyl Alcohol-Degrading Strain Sphingopyxis sp. 113P3 (NBRC 111507)

    PubMed Central

    Nagata, Yuji; Numata, Mitsuru; Tsuchikane, Kieko; Hosoyama, Akira; Yamazoe, Atsushi; Tsuda, Masataka; Fujita, Nobuyuki; Kawai, Fusako

    2015-01-01

    Strain 113P3 was isolated from activated sludge and identified as a polyvinyl alcohol (PVA)-degrading Pseudomonas species; it was later reidentified as Sphingopyxis species. Only three genes are directly relevant to the metabolism of PVA and comprise the pva operon, which was deposited as accession no. AB190228. Here, we report the complete genome sequence of strain 113P3, which has been conserved as a stock culture (NBRC 111507) at the Biological Resource Center, National Institute of Technology and Evaluation (NITE) (Tokyo, Japan). The genome of strain 113P3 is composed of a 4.4-Mb circular chromosome and a 243-kb plasmid. The whole finishing was conducted in silico except for four PCRs. The sequence corresponding to AB190288 exists on the chromosome. PMID:26472829

  4. Effect of different polyol-based plasticizers on thermal properties of polyvinyl alcohol:starch blends.

    PubMed

    Ayd?n, Ahmet Alper; Ilberg, Vladimir

    2016-01-20

    A series of gelatinized polyvinyl alcohol (PVA):starch blends were prepared with various polyol-based plasticizers in 5wt%, 15wt% and 25wt% ratios via solution casting method. The obtained films were analyzed by Fourier transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Remarkable changes have been observed in glass-transition temperature (Tg) and thermal stability of the samples containing varying concentrations of different plasticizers and they have been discussed in detail with respect to the conducted thermal and chemical analyses. The observed order of Tg point depression of the samples containing 15wt% plasticizer is 1,4-butanediol - 1,2,6-hexanetriol - pentaerythriyol - xylitol - mannitol, which is similar to the sequence of the thermal stability changes of the samples. PMID:26572374

  5. PIXE investigation of in vitro release of chloramphenicol across polyvinyl alcohol/acrylamide hydrogel

    NASA Astrophysics Data System (ADS)

    Rihawy, M. S.; Alzier, A.; Allaf, A. W.

    2011-09-01

    Hydrogels based on polyvinyl alcohol and different amounts of acrylamide monomer were prepared by thermal cross-linking in the solid state. The hydrogels were investigated for drug delivery system applications. Chloramphenicol was adopted as a model drug to study its release behavior. Particle induced X-ray emission was utilized to study the drug release behavior across the hydrogels and a comparison study with ultraviolet measurements was performed. Fourier Transform Infrared measurements were carried out for molecular characterization. The releasing behavior of the drug exhibits a decrease and a subsequent increase in the release rate, as the acrylamide monomer increases. Characterization of the hydrogels has shown a competitive behavior between crosslinking with AAm acrylamide monomer or oligomerized version, depending on the amount added to prepare the hydrogels.

  6. Antibacterial surfaces by adsorptive binding of polyvinyl-sulphonate-stabilized silver nanoparticles

    NASA Astrophysics Data System (ADS)

    Vasilev, Krasimir; Sah, Vasu R.; Goreham, Renee V.; Ndi, Chi; Short, Robert D.; Griesser, Hans J.

    2010-05-01

    This paper presents a novel and facile method for the generation of efficient antibacterial coatings which can be applied to practically any type of substrate. Silver nanoparticles were stabilized with an adsorbed surface layer of polyvinyl sulphonate (PVS). This steric layer provided excellent colloidal stability, preventing aggregation over periods of months. PVS-coated silver nanoparticles were bound onto amine-containing surfaces, here produced by deposition of an allylamine plasma polymer thin film onto various substrates. SEM imaging showed no aggregation upon surface binding of the nanoparticles; they were well dispersed on amine surfaces. Such nanoparticle-coated surfaces were found to be effective in preventing attachment of Staphylococcus epidermidis bacteria and also in preventing biofilm formation. Combined with the ability of plasma polymerization to apply the thin polymeric binding layer onto a wide range of materials, this method appears promising for the fabrication of a wide range of infection-resistant biomedical devices.

  7. A polyvinyl alcohol-functionalized sorbent for extraction and determination of aminoglycoside antibiotics in honey.

    PubMed

    Wang, Yuan; Ji, Shunli; Zhang, Feng; Zhang, Feifang; Yang, Bingcheng; Liang, Xinmiao

    2015-07-17

    A novel highly hydrophilic sorbent simply prepared by coating polyvinyl alcohol (PVA) onto silica gel was used for extraction and determination of aminoglycoside antibiotics (AAs). The fabricated PVA coating is aimed to effectively protect core silica gel inside and offers good hydrophilic property. In combination of hydrophilic interaction chromatography tandem mass spectrometry, the performance of the sorbent was evaluated by selecting four model AAs (dihydrostreptomycin, streptomycin, kanamycin, spectinomycin). The sorbent was found to have effective adsorption ability to hydrophilic AAs, which was superior or comparable to those of commercial ones. Good recoveries (84-112%) of model AAs spiked in honey were obtained with good precision (<12.4%) and the limit of quantitation for the proposed method was in the range of 7.8-19.4ng/mL. PMID:26047525

  8. Complete Genome Sequence of Polyvinyl Alcohol-Degrading Strain Sphingopyxis sp. 113P3 (NBRC 111507).

    PubMed

    Ohtsubo, Yoshiyuki; Nagata, Yuji; Numata, Mitsuru; Tsuchikane, Kieko; Hosoyama, Akira; Yamazoe, Atsushi; Tsuda, Masataka; Fujita, Nobuyuki; Kawai, Fusako

    2015-01-01

    Strain 113P3 was isolated from activated sludge and identified as a polyvinyl alcohol (PVA)-degrading Pseudomonas species; it was later reidentified as Sphingopyxis species. Only three genes are directly relevant to the metabolism of PVA and comprise the pva operon, which was deposited as accession no. AB190228. Here, we report the complete genome sequence of strain 113P3, which has been conserved as a stock culture (NBRC 111507) at the Biological Resource Center, National Institute of Technology and Evaluation (NITE) (Tokyo, Japan). The genome of strain 113P3 is composed of a 4.4-Mb circular chromosome and a 243-kb plasmid. The whole finishing was conducted in silico except for four PCRs. The sequence corresponding to AB190288 exists on the chromosome. PMID:26472829

  9. Method of cross-linking polyvinyl alcohol and other water soluble resins

    NASA Technical Reports Server (NTRS)

    Phillipp, W. H.; May, C. E.; Hsu, L. C.; Sheibley, D. W. (inventors)

    1980-01-01

    A self supporting sheet structure comprising a water soluble, noncrosslinked polymer such as polyvinyl alcohol which is capable of being crosslinked by reaction with hydrogen atom radicals and hydroxyl molecule radicals is contacted with an aqueous solution having a pH of less than 8 and containing a dissolved salt in an amount sufficient to prevent substantial dissolution of the noncrosslinked polymer in the aqueous solution. The aqueous solution is then irradiated with ionizing radiation to form hydrogen atom radicals and hydroxyl molecule radicals and the irradiation is continued for a time sufficient to effect crosslinking of the water soluble polymer to produce a water insoluble polymer sheet structure. The method has particular application in the production of battery separators and electrode envelopes for alkaline batteries.

  10. Highly water-dispersible silver sulfadiazine decorated with polyvinyl pyrrolidone and its antibacterial activities.

    PubMed

    Li, Ping; Wu, Longlong; Li, Binjie; Zhao, Yanbao; Qu, Peng

    2016-03-01

    Highly water-dispersible silver sulfadiazine (SSD) was prepared by liquid phase method with polyvinyl pyrrolidone (PVP) as a surface modification agent. The structure and morphology of the PVP-modified silver sulfadiazine (P-SSD) were investigated by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), thermogravimetric analysis (TGA) and Fourier-transform infrared (FT-IR) spectrometry. The produced particles are ginkgo leaf-like architecture with the sizes of micron-nanometer. Due to hydrophilic PVP decorated on the surface, the P-SSD has excellent dispersion in water over a period of 24h, which is obviously stable by comparison to that of the commercial silver sulfadiazine (C-SSD). In addition, the P-SSD exhibits good antibacterial activities against Escherichia coli (E. coli), Pseudomonas aeruginosa (P. aeruginosa) and Staphylococcus aureus (S. aureus). PMID:26706506

  11. Copper-containing polyvinyl alcohol composite systems: Preparation, characterization and biological activity

    NASA Astrophysics Data System (ADS)

    Reza Hajipour, Abdol; Mohammadsaleh, Fatemeh; Reza Sabzalian, Mohammad

    2015-08-01

    The present investigation reports, the complex formation of Cu(II) with polyvinyl alcohol (PVA) and the synthesis of PVA-stabilized Cu2O particles. This PVA-Cu2O composite has been prepared via chemical reduction method using PVA-Cu(II) complex as precursor. At first, Cu(II) ions were stabilized in PVA matrix via complex formation with OH groups; subsequently, this PVA-Cu(II) macromolecular complex as precursor reacted with ascorbic acid as reducing agent at pH=12 to prepare PVA-Cu2O composite. The products were characterized by FTIR, XRD, FE-SEM, HRTEM, Visible Spectroscopy and atomic absorption. In the following, the antibacterial properties of as-prepared composites were examined against Gram-positive (Bacillus thuringiensis) and Gram-negative bacteria (Escherichia coli), and the results showed excellent antibacterial activity of these materials.

  12. Antimicrobial wound dressing nanofiber mats from multicomponent (chitosan/silver-NPs/polyvinyl alcohol) systems.

    PubMed

    Abdelgawad, Abdelrahman M; Hudson, Samuel M; Rojas, Orlando J

    2014-01-16

    Novel hybrid nanomaterials have been developed for antimicrobial applications. Here we introduce a green route to produce antibacterial nanofiber mats loaded with silver nanoparticles (Ag-NPs, 25 nm diameter) enveloped in chitosan after reduction with glucose. The nanofiber mats were obtained from colloidal dispersions of chitosan-based Ag-NPs blended with polyvinyl alcohol. Nanofibers (150 nm average diameter and narrow size distribution) were obtained by electrospinning and cross-linked with glutaraldhyde. The effect of crosslinking on the release of silver was studied by atomic absorption spectroscopy. Antimicrobial activity was studied by the viable cell-counting; mats loaded with silver and control samples (chitosan/PVA) with different degrees of cross-linking were compared for their effectiveness in reducing or halting the growth of aerobic bacteria. The results showed superior properties and synergistic antibacterial effects by combining chitosan with Ag-NPs. PMID:24188851

  13. Electrospun polyvinyl alcohol-collagen-hydroxyapatite nanofibers: a biomimetic extracellular matrix for osteoblastic cells

    NASA Astrophysics Data System (ADS)

    Song, Wei; Markel, David C.; Wang, Sunxi; Shi, Tong; Mao, Guangzhao; Ren, Weiping

    2012-03-01

    The failure of prosthesis after total joint replacement is due to the lack of early implant osseointegration. In this study polyvinyl alcohol-collagen-hydroxyapatite (PVA-Col-HA) electrospun nanofibrous meshes were fabricated as a biomimetic bone-like extracellular matrix for the modification of orthopedic prosthetic surfaces. In order to reinforce the PVA nanofibers, HA nanorods and Type I collagen were incorporated into the nanofibers. We investigated the morphology, biodegradability, mechanical properties and biocompatibility of the prepared nanofibers. Our results showed these inorganic-organic blended nanofibers to be degradable in vitro. The encapsulated nano-HA and collagen interacted with the PVA content, reinforcing the hydrolytic resistance and mechanical properties of nanofibers that provided longer lasting stability. The encapsulated nano-HA and collagen also enhanced the adhesion and proliferation of murine bone cells (MC3T3) in vitro. We propose the PVA-Col-HA nanofibers might be promising modifying materials on implant surfaces for orthopedic applications.

  14. Study of polyvinyl alcohol nanofibrous membrane by electrospinning as a magnetic nanoparticle delivery approach

    SciTech Connect

    Ger, Tzong-Rong; Huang, Hao-Ting; Hu, Keng-Shiang; Huang, Chen-Yu; Lai, Jun-Yang; Chen, Jiann-Yeu; Lai, Mei-Feng

    2014-05-07

    Electrospinning technique was used to fabricate polyvinyl alcohol (PVA)-based magnetic biodegradable nanofibers. PVA solution was mixed with ferrofluid or magnetic nanoparticles (MNPs) powder and formed two individual nanofibrous membranes (PVA/ferrofluid and PVA/MNPs powder) by electrospinning. The surface morphology of the nanofibrous membrane was characterized by scanning electron microscopy and the magnetic properties were measured by vibrating sample magnetometer. Macrophages (RAW 264.7) were co-cultured with the nanofibrous membranes for 12, 24, and 48 h and exhibited good cell viability (>95%). Results showed that the PVA fibers would be degraded and the embedded Fe{sub 3}O{sub 4} nanoparticles would be released and delivered to cells.

  15. Effects of PVA(Polyvinyl Alcohol) on Supercooling Phenomena of Water

    NASA Astrophysics Data System (ADS)

    Kumano, Hiroyuki; Saito, Akio; Okawa, Seiji; Takizawa, Hiroshi

    In this paper, effects of polymer additive on supercooling of water were investigated experimentally. Poly-vinyl alcohol (PVA) were used as the polymer, and the samples were prepared by dissolving PVA in ultra pure water. Concentration, degree of polymerization and saponification of PVA were varied as the experimental parameters. The sample was cooled, and the temperature at the instant when ice appears was measured. Since freezing of supercooled water is statistical phenomenon, many experiments were carried out and average degrees of supercooling were obtained for each experimental condition. As the result, it was found that PVA affects nucleation of supercooling and the degree of supercooling increases by adding the PVA. Especially, it is found that the average degree of supercooling increases and the standard deviation of average degree of supercooling decreases with increase of degree of saponification of PVA. However, the average degree of supercooling are independent of the degree of polymerization of PVA in the range of this study.

  16. Antimicrobial-coated polypropylene films with polyvinyl alcohol in packaging of fresh beef.

    PubMed

    Han, Chunyang; Wang, Jianqing; Li, Yang; Lu, Fei; Cui, Yan

    2014-02-01

    The utility of packaging films consisting of cast polypropylene/polyvinyl alcohol with rhubarb ethanolic extracts (REE) and cinnamon essential oil (CEO) in maintaining fresh beef quality was investigated. Fresh beefsteaks were packed with antimicrobial films containing different concentrations of REE and CEO. Beef characteristics, including pH, total viable counts, instrumentally measured color, weight loss, total volatile base nitrogen (TVB-N) and sensory quality were determined. All experimental films significantly inhibited bacterial growth (p<0.05) and maintained the pH and TVB-N of beefsteaks. Three of four experimental films significantly reduced instrumental color loss (p<0.05). Antimicrobial packaging films efficiently maintained the quality of fresh beefsteaks during storage. PMID:24211547

  17. Anaerobic digestion of starch-polyvinyl alcohol biopolymer packaging: biodegradability and environmental impact assessment.

    PubMed

    Guo, M; Trzcinski, A P; Stuckey, D C; Murphy, R J

    2011-12-01

    The digestibility of a starch-polyvinyl alcohol (PVOH) biopolymer insulated cardboard coolbox was investigated under a defined anaerobic digestion (AD) system with key parameters characterized. Laboratory results were combined with industrial operational data to develop a site-specific life cycle assessment (LCA) model. Inoculated with active bacterial trophic groups, the anaerobic biodegradability of three starch-PVOH biopolymers achieved 58-62%. The LCA modeling showed that the environmental burdens of the starch-PVOH biopolymer packaging under AD conditions on acidification, eutrophication, global warming and photochemical oxidation potential were dominated by atmospheric emissions released from substrate degradation and fuel combustion, whereas energy consumption and infrastructure requirements were the causes of abiotic depletion, ozone depletion and toxic impacts. Nevertheless, for this bio-packaging, AD of the starch-PVOH biopolymer combined with recycling of the cardboard emerged as the environmentally superior option and optimization of the energy utilization system could bring further environmental benefits to the AD process. PMID:22001054

  18. A stimuli-responsive and bioactive film based on blended polyvinyl alcohol and cashew gum polysaccharide.

    PubMed

    Silva, Fábio E F; Batista, Karla A; Di-Medeiros, Maria C B; Silva, Cassio N S; Moreira, Bruna R; Fernandes, Kátia F

    2016-01-01

    In this study, a stimuli-responsive, biodegradable and bioactive film was produced by blending cashew gum polysaccharide (CGP) and polyvinyl alcohol (PVA). The film presented malleability and mechanical properties enabling an easy handling. Wetting the film changed the optical property from opacity to levels of transparency higher than 70% and resulted in up to 2-fold increase in its superficial area. Different swelling indexes were obtained varying the pH of solvent, which allows classifying the CGP/PVA film as pH sensitive stimuli-responsive material. The bioactivity was achieved through covalent immobilization of papain, which remained active after storage of CGP/PVA-papain film for 24h in the presence of buffer or in a dry form. These results evidenced that CGP/PVA-papain film is a very promising material for biomedical applications. PMID:26478388

  19. Antibacterial surfaces by adsorptive binding of polyvinyl-sulphonate-stabilized silver nanoparticles.

    PubMed

    Vasilev, Krasimir; Sah, Vasu R; Goreham, Renee V; Ndi, Chi; Short, Robert D; Griesser, Hans J

    2010-05-28

    This paper presents a novel and facile method for the generation of efficient antibacterial coatings which can be applied to practically any type of substrate. Silver nanoparticles were stabilized with an adsorbed surface layer of polyvinyl sulphonate (PVS). This steric layer provided excellent colloidal stability, preventing aggregation over periods of months. PVS-coated silver nanoparticles were bound onto amine-containing surfaces, here produced by deposition of an allylamine plasma polymer thin film onto various substrates. SEM imaging showed no aggregation upon surface binding of the nanoparticles; they were well dispersed on amine surfaces. Such nanoparticle-coated surfaces were found to be effective in preventing attachment of Staphylococcus epidermidis bacteria and also in preventing biofilm formation. Combined with the ability of plasma polymerization to apply the thin polymeric binding layer onto a wide range of materials, this method appears promising for the fabrication of a wide range of infection-resistant biomedical devices. PMID:20431209

  20. Microporous poly(vinyl methyl ether) hydrogels prepared by ?-ray irradiation at different heating rates

    NASA Astrophysics Data System (ADS)

    Kishi, Ryoichi; Kihara, Hideyuki; Miura, Toshiaki; Ichijo, Hisao

    2005-04-01

    We prepared thermoresponsive and microporous polymer hydrogels by ?-ray irradiation of aqueous solutions poly(vinyl methyl ether) (PVME) at different heating rates. Under all temperature programs, opaque and heterogeneous PVME gels formed, which swelled at temperatures below the lower critical solution temperature and shrank at temperatures above it. All of the samples contained porous and phase-separated structures. The shape and size of the gel pores varied depending on the temperature programs. Gels having a sponge-like continuous porous structure formed only when the radiation-induced crosslinking was carried out at an optimum heating rate, which we found to be 0.11-0.13°C min -1. For temperature changes between 10°C and 40°C, gels with this structure showed rapid volume transitions on a time scale of about a minute.

  1. Improvement of polyvinyl alcohol properties by adding nanocrystalline cellulose isolated from banana pseudostems.

    PubMed

    Pereira, André Luís S; do Nascimento, Diego M; Souza Filho, Men de Sá M; Morais, João Paulo S; Vasconcelos, Niedja F; Feitosa, Judith P A; Brígida, Ana Iraidy S; Rosa, Morsyleide de F

    2014-11-01

    Cellulose nanocrystals (CNCs) isolated from banana pseudostems fibers (BPF) of the Pacovan variety were used as fillers in a polyvinyl alcohol (PVOH) matrix to yield a nanocomposite. The fibers from the external fractions of the BPF were alkaline bleached and hydrolyzed under acidic conditions (H2SO4 62% w/w, 70 min, 45 °C) to obtain CNCs with a length (L) of 135.0 ± 12.0 nm and a diameter (D) of 7.2 ± 1.9 nm to yield an aspect ratio (L/D) of 21.2. The CNCs were applied to PVOH films at different concentrations (0%, 1%, 3%, and 5% w/w, dry basis). With higher concentrations of CNCs, the water-vapor barrier of the films increased, while the optical properties changed very little. Increasing the concentration of the CNCs up to 3% significantly improved the mechanical properties of the nanocomposite. PMID:25129731

  2. Spectroelectrochemical Studies on Quinacridone by Using Poly(vinyl alcohol) Coating as Protection Layer.

    PubMed

    Enengl, Sandra; Enengl, Christina; Stadler, Philipp; Neugebauer, Helmut; Sariciftci, Niyazi Serdar

    2015-07-20

    Spectroscopic measurements in the infrared range combined with electrochemistry are a powerful technique for investigation of organic semiconductors to track changes during oxidation and reduction (p- and n-doping) processes. For these measurements it is important that the studied material, mostly deposited as a thin film on an internal reflection element, does not dissolve during this characterization. In this study we introduce a technique that allows infrared spectroelectrochemical characterization of films of these materials for the first time. In many cases so far this has been impossible, due to solubility in the oxidized and/or reduced form. This novel technique is shown on thin films of quinacridone by adding a protection layer of poly(vinyl alcohol) (PVA). PMID:26013836

  3. Asymmetric supercapacitor based on nanostructured graphene foam/polyvinyl alcohol/formaldehyde and activated carbon electrodes

    NASA Astrophysics Data System (ADS)

    Bello, Abdulhakeem; Barzegar, Farshad; Momodu, Damilola; Dangbegnon, Julien; Taghizadeh, Fatemeh; Fabiane, Mopeli; Manyala, Ncholu

    2015-01-01

    We present the electrochemical results of highly porous and interconnected carbon material by activation of graphene foam/polyvinyl alcohol-formaldehyde composite material designated as GF/PVA-F. Asymmetric supercapacitor devices were fabricated using the activated material (GF/PVA-F) and activated carbon (AC) as the positive and negative electrodes respectively. The device exhibited a maximum energy density of 42 mWh cm-2, a power density of 0.5 W cm-2 and 98% retention of its initial capacitance after 2000 cycles in an extended cell potential window of 1.8 V in 1 M Na2SO4 aqueous electrolyte. This work shows the great potential of this material for high performance energy storage application.

  4. All solid-state electric double-layer capacitors based on alkaline polyvinyl alcohol polymer electrolytes

    NASA Astrophysics Data System (ADS)

    Yang, Chun-Chen; Hsu, Sung-Ting; Chien, Wen-Chen

    Solid-state electrochemical double-layer capacitors (ELDCs) based on alkaline polyvinyl alcohol (PVA) solid polymer electrolytes (SPEs) are prepared. Electrochemical capacitance performance of these capacitors is studied by cyclic voltammetry, galvanostatic charge-discharge testing, and ac impedance spectroscopy. For comparison, two types of EDLC cells are constructed and tested. It is found that an EDLC with a PVA polymer electrolyte exhibits much higher capacitance and longer cycle-life than one with the PP/PE separator. The specific capacitance for the EDLC with the PVA-based SPE is in the range of 100-112 F g -1, and depends on the scan rate or the charge-discharge current rates. The results also indicate that the solid-state EDLC shows a relatively stable specific capacitance of 100 F g -1 after 1000 cycles. The findings suggest that the PVA-based SPE is a promising material for use in EDLCs.

  5. Effect of Adhesion and Contact Geometry on Scratch Behavior of Polyvinyl Alcohol

    NASA Astrophysics Data System (ADS)

    Yoder, Karl; Xia, Xinyun; Gerberich, William

    2000-03-01

    The mechanical response of a material to single-point scratch loading is complex, with contributions from contact geometry, imposed deformation rate, thermomechanical interactions, and constitutive properties. Additionally, the effect of adhesion between scratch tip and specimen is an important, yet poorly understood, variable in deformation response. In particular the effects of adhesion and contact geometry on the mode of deformation and damage morphology are difficult to experimentally separate. Using a Hysitron Triboindenter, which can perform both nanoindentation and nanoscratch tests, in a controlled environmental chamber, the effect of adhesion on scratch response of polyvinyl alcohol is investigated. In addition, by using four different diamond tips, the role of contact geometry as it pertains to adhesion and scratch response is investigated. This talk presents the effects of contact geometry and relative humidity on stylus-PVOH adhesion, and subsequent scratch deformation response in an attempt to elucidate the role played by adhesion.

  6. Investigation of polypyrrole/polyvinyl alcohol-titanium dioxide composite films for photo-catalytic applications

    NASA Astrophysics Data System (ADS)

    Cao, Shaoqiang; Zhang, Hongyang; Song, Yuanqing; Zhang, Jianling; Yang, Haigang; Jiang, Long; Dan, Yi

    2015-07-01

    Polypyrrole/polyvinyl alcohol-titanium dioxide (PPy/PVA-TiO2) composite films used as photo-catalysts were fabricated by combining TiO2 sol with PPy/PVA solution in which PPy was synthesized by in situ polymerization of pyrrole (Py) in polyvinyl alcohol (PVA) matrix and loaded on glass. The prepared photo-catalysts were investigated by X-ray diffraction (XRD), ultraviolet-visible diffuse reflection spectroscopy (UV-vis DRS), scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) spectra and photoluminescence (PL). The results indicate that the composites have same crystal structure as the TiO2 and extend the optic absorption from UV region to visible light region. By detecting the variation ratio, detected by ultraviolet-vis spectroscopy, of model pollutant rhodamine B (RhB) solution in the presence of the composite films under both UV and visible light irradiation, the photo-catalytic performance of the composite films was investigated. The results show that the PPy/PVA-TiO2 composite films show better photo-catalytic properties than TiO2 film both under UV and visible light irradiation, and the photo-catalytic degradation of RhB follows the first-order kinetics. The effects of the composition of composite films and the concentration of RhB on the photo-catalytic performance, as well as the possible photo-catalytic mechanism, were also discussed. By photo-catalytic recycle experiments, the structure stability of the PPy/PVA-TiO2 composite film was investigated and the results show that the photo-catalytic activity under both UV and visible light irradiation have no significant decrease after four times of recycle experiments, suggesting that the photo-catalyst film is stable during the photo-catalytic process, which was also confirmed by the XRD pattern and FT-IR spectra of the composite film before and after photo-catalytic.

  7. Fate and residues of trenbolone acetate in edible tissues from sheep amd calves implanted with tritium-labeled trenbolone acetate

    SciTech Connect

    Evrard, P.; Maghuin-Rogister, G.; Rico, A.G. )

    1989-06-01

    In order to study the fate and residues of trenbolone acetate in edible tissues, two groups of six animals from two ruminant species (ewes and calves) were implanted with (3H)trenbolone acetate. The distribution of extractable radioactive residues was measured in liver, kidney and muscle. We found that the largest proportion of residues was not extractable and thus was considered as covalently bound residues. The proportion of the main extractable metabolites (17 alpha-trenbolone, trendione, 17 beta-trenbolone) was measured. The evaluation of the distribution of trenbolone acetate metabolites directly soluble in water showed that unknown metabolite(s) were predominant. The covalent binding to nucleic acids was measured. It was so low that it was not detectable. The results are discussed in light of the data presented in the scientific report on anabolic agents in animal production from the European scientific working group.

  8. Tarapacol 15-Acetate, a New Diterpenoid from Grindelia tarapacana Phil.

    E-print Network

    Zhou, Lin; Timmermann, Barbara N.; Grittini, Carina; Bruck, Michael A.; Enemark, John H.

    1996-01-01

    In the title compound, 15-acetoxy-14(S)-hydroxy-13-epi-manoyl oxide {IUPAC systematic name: 2-(dodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran-3-yl)-2-hydroxyethyl acetate}, C22H38N4, rings A and B have chair conformations. Ring C adopts...

  9. Fragrance material review on p-isopropylbenzyl acetate.

    PubMed

    McGinty, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of p-isopropylbenzyl acetate when used as a fragrance ingredient is presented. p-Isopropylbenzyl acetate is a member of the fragrance structural group Aryl Alkyl Alcohol Simple Acid Esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1 to 4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for p-isopropylbenzyl acetate were evaluated, then summarized, and includes: physical properties, acute toxicity, skin irritation, and skin sensitization data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22406560

  10. Electrodeposition of Californium Using Isobutanol and Aqueous Ammonium Acetate

    NASA Astrophysics Data System (ADS)

    Matoš, Milan; Boll, Rose A.; Phelps, Clarice E.; Torrico, Matthew N.; van Cleve, Shelley M.; Lewis, Benjamin E.

    2013-10-01

    Californium sources and targets are used in many applications in research and industry. Molecular deposition (commonly referred to as electrodeposition) is an experimental technique suitable for production of californium thin films. We are investigating molecular depositions using isobutanol and aqueous ammonium acetate solvents at various conditions to optimize for the best deposition efficiency and repeatability. Results of those tests will be presented.

  11. Thermodynamic analysis of acetic acid steam reforming for hydrogen production

    NASA Astrophysics Data System (ADS)

    Goicoechea, Saioa; Ehrich, Heike; Arias, Pedro L.; Kockmann, Norbert

    2015-04-01

    A thermodynamic analysis of hydrogen generation by acetic acid steam reforming has been carried out with respect to applications in solid oxide fuel cells. The effect of operating parameters on equilibrium composition has been examined focusing especially on hydrogen and carbon monoxide production, which are the fuels in this type of fuel cell. The temperature, steam to acetic acid ratio, and to a lesser extent pressure affect significantly the equilibrium product distribution due to their influence on steam reforming, thermal decomposition and water-gas shift reaction. The study shows that steam reforming of acetic acid with a steam to acetic acid ratio of 2 to 1 is thermodynamically feasible with hydrogen, carbon monoxide and water as the main products at the equilibrium at temperatures higher than 700 °C, and achieving CO/CO2 ratios higher than 1. Thus, it can be concluded that within the operation temperature range of solid oxide fuel cells - between 700 °C and 1000 °C - the production of a gas rich in hydrogen and carbon monoxide is promoted.

  12. Lithium acetate transformation of yeast Maitreya Dunham August 2004

    E-print Network

    Dunham, Maitreya

    Lithium acetate transformation of yeast Maitreya Dunham August 2004 Original protocol from Katja at room temperature on the orbital shaker. Mix: 10 µl 10 mg/ml boiled sheared salmon sperm DNA ~10 µl ~5-10 µg DNA (also set up a ­DNA control) 200 µl cells Incubate 30 min at room temperature on the orbital

  13. Fragrance material review on 2,4-dimethylbenzyl acetate.

    PubMed

    McGinty, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of 2,4-dimethylbenzyl acetate when used as a fragrance ingredient is presented. 2,4-Dimethylbenzyl acetate is a member of the fragrance structural group aryl alkyl alcohol simple acid esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, iso-butyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for 2,4-dimethylbenzyl acetate were evaluated, then summarized, and includes: physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, and skin sensitization data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22414641

  14. Fragrance material review on p-anisyl acetate.

    PubMed

    McGinty, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of p-anisyl acetate when used as a fragrance ingredient is presented. p-Anisyl acetate is a member of the fragrance structural group aryl alkyl alcohol simple acid esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for p-anisyl acetate were evaluated, then summarized, and includes: physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, and genotoxicity data. A safety assessment of the entire AAASAE will be published simultaneously with this document. Please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22417777

  15. Fragrance material review on ethyl phenyl carbinyl acetate.

    PubMed

    McGinty, D; Letizia, C S; Api, A M

    2012-09-01

    A toxicologic and dermatologic review of ethyl phenyl carbinyl acetate when used as a fragrance ingredient is presented. Ethyl phenyl carbinyl acetate is a member of the fragrance structural group Aryl Alkyl Alcohol Simple Acid Esters (AAASAE). The AAASAE fragrance ingredients are prepared by reacting an aryl alkyl alcohol with a simple carboxylic acid (a chain of 1-4 carbons) to generate formate, acetate, propionate, butyrate, isobutyrate and carbonate esters. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for ethyl phenyl carbinyl acetate were evaluated, then summarized, and includes: physical properties; acute toxicity; skin irritation; and skin sensitization data. A safety assessment of the entire AAASAE will be published simultaneously with this document; please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all AAASAE in fragrances. PMID:22433983

  16. PROCESS FOR OBTAINING CELLULOSE ACETATE FROM AGRICULTURAL BY-PRODUCTS

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A method of preparation of commercially useful product, cellulose acetate from discarded byproducts such as rice-straw, wheat hull and corn fiber will be discussed. This work will provide potential new markets and applications for low-value agricultural wastes and co-products. By converting the ce...

  17. THERMOREGULATION IN MICE FOLLOWING ACUTE ADMINISTRATION OF LEAD ACETATE

    EPA Science Inventory

    Several reports in the literature suggest a relationship between lead intoxication and thermoregulatory capacity. To investigate the effects of lead on the control of body temperature, mice of the BALB/c strain were injected intraperitoneally with lead acetate (0 to 100 mg/kg) wh...

  18. 21 CFR 584.200 - Ethyl alcohol containing ethyl acetate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...added the equivalent of 4.25 gallons of 100 percent ethyl acetate. It is used in accordance with good feeding practices in ruminant feed supplements as a source of added energy. [46 FR 52333, Oct. 27, 1981, as amended at 72 FR 41620, July 31,...

  19. Condensation of acetol and acetic acid vapor with sprayed liquid

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A cellulose-derived fraction of biomass pyrolysis vapor was simulated by evaporating acetol and acetic acid (AA) from flasks on a hot plate. The liquid in the flasks was infused with heated nitrogen. The vapor/nitrogen stream was superheated in a tube oven and condensed by contact with a cloud of ...

  20. Poly(vinyl ester 1,2,3-triazolium)s: a new member of the poly(ionic liquid)s family.

    PubMed

    Obadia, M M; Colliat-Dangus, G; Debuigne, A; Serghei, A; Detrembleur, C; Drockenmuller, E

    2015-02-25

    A vinyl ester monomer carrying a pendant 1,2,3-triazole group is synthesized in two steps and polymerized by cobalt-mediated radical polymerization. Subsequent alkylation with N-methyl bis[(trifluoromethyl)sulfonyl]imide affords the corresponding poly(vinyl ester 1,2,3-triazolium). This unprecedented example of poly(vinyl ester ionic liquid) exhibits an ionic conductivity of 9.2 × 10(-7) S cm(-1) at 30 °C. PMID:25588063

  1. Stochastic model prediction of the Kovacs' ``expansion gap'' effect for volume relaxation in glassy polymers

    NASA Astrophysics Data System (ADS)

    Medvedev, Grigori; Caruthers, James

    2015-03-01

    The classic series of experiments by A. Kovacs on volume relaxation following temperature jumps for poly(vinyl acetate), PVAc, in the Tg region revealed the richness and complexity of the viscoelastic behavior of glassy materials. Over the years no theoretical model has been able to predict all the features of the Kovacs data, where the so-called ``expansion gap'' effect proved to be particularly challenging. Specifically, for a series of up-jump experiments with different initial temperatures, Ti, but with the same final temperature, as the relaxation approaches equilibrium it would be expected that the effective relaxation time would be the same regardless of Ti; however, Kovacs observed that the dependence on Ti persisted seemingly all the way to equilibrium. In this communication we will show that a recently developed Stochastic Constitutive Model (SCM) that explicitly acknowledges the nano-scale dynamic heterogeneity of glasses can capture the ``expansion gap'' as well as the rest of the Kovacs data set for PVAc. It will be shown that the success of the SCM is due to its inherent thermo-rheological complexity.

  2. The Key to Acetate: Metabolic Fluxes of Acetic Acid Bacteria under Cocoa Pulp Fermentation-Simulating Conditions

    PubMed Central

    Adler, Philipp; Frey, Lasse Jannis; Berger, Antje; Bolten, Christoph Josef; Hansen, Carl Erik

    2014-01-01

    Acetic acid bacteria (AAB) play an important role during cocoa fermentation, as their main product, acetate, is a major driver for the development of the desired cocoa flavors. Here, we investigated the specialized metabolism of these bacteria under cocoa pulp fermentation-simulating conditions. A carefully designed combination of parallel 13C isotope labeling experiments allowed the elucidation of intracellular fluxes in the complex environment of cocoa pulp, when lactate and ethanol were included as primary substrates among undefined ingredients. We demonstrate that AAB exhibit a functionally separated metabolism during coconsumption of two-carbon and three-carbon substrates. Acetate is almost exclusively derived from ethanol, while lactate serves for the formation of acetoin and biomass building blocks. Although this is suboptimal for cellular energetics, this allows maximized growth and conversion rates. The functional separation results from a lack of phosphoenolpyruvate carboxykinase and malic enzymes, typically present in bacteria to interconnect metabolism. In fact, gluconeogenesis is driven by pyruvate phosphate dikinase. Consequently, a balanced ratio of lactate and ethanol is important for the optimum performance of AAB. As lactate and ethanol are individually supplied by lactic acid bacteria and yeasts during the initial phase of cocoa fermentation, respectively, this underlines the importance of a well-balanced microbial consortium for a successful fermentation process. Indeed, AAB performed the best and produced the largest amounts of acetate in mixed culture experiments when lactic acid bacteria and yeasts were both present. PMID:24837393

  3. 21 CFR 529.1003 - Flurogestone acetate-impregnated vaginal sponge.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...Flurogestone acetate-impregnated vaginal sponge. 529.1003 Section 529.1003 Food...Flurogestone acetate-impregnated vaginal sponge. (a) Specifications. Each vaginal sponge contains 20 milligrams of flurogestone...

  4. 21 CFR 529.1003 - Flurogestone acetate-impregnated vaginal sponge.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...Flurogestone acetate-impregnated vaginal sponge. 529.1003 Section 529.1003 Food...Flurogestone acetate-impregnated vaginal sponge. (a) Specifications. Each vaginal sponge contains 20 milligrams of flurogestone...

  5. 40 CFR 721.10448 - Acetic acid, hydroxy- methoxy-, methyl ester, reaction products with substituted alkylamine...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... ester, reaction products with substituted alkylamine (generic). 721.10448 Section 721.10448 Protection... Acetic acid, hydroxy- methoxy-, methyl ester, reaction products with substituted alkylamine (generic). (a... generically as acetic acid, hydroxymethoxy-, methyl ester, reaction products with substituted alkylamine...

  6. 40 CFR 721.10448 - Acetic acid, hydroxy- methoxy-, methylester, reaction products with substituted alkylamine...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...-, methylester, reaction products with substituted alkylamine (generic). 721.10448 Section 721.10448 Protection... Acetic acid, hydroxy- methoxy-, methylester, reaction products with substituted alkylamine (generic). (a... generically as acetic acid, hydroxymethoxy-, methyl ester, reaction products with substituted alkylamine...

  7. 21 CFR 862.1390 - 5-Hydroxyindole acetic acid/serotonin test system.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...DEVICES Clinical Chemistry Test Systems § 862.1390 5-Hydroxyindole...acetic acid/serotonin test system. (a) Identification...acetic acid/serotonin test system is a device intended to...treatment of carcinoid tumors of endocrine tissue. (b)...

  8. 21 CFR 862.1390 - 5-Hydroxyindole acetic acid/serotonin test system.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...DEVICES Clinical Chemistry Test Systems § 862.1390 5-Hydroxyindole...acetic acid/serotonin test system. (a) Identification...acetic acid/serotonin test system is a device intended to...treatment of carcinoid tumors of endocrine tissue. (b)...

  9. 21 CFR 862.1390 - 5-Hydroxyindole acetic acid/serotonin test system.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...DEVICES Clinical Chemistry Test Systems § 862.1390 5-Hydroxyindole...acetic acid/serotonin test system. (a) Identification...acetic acid/serotonin test system is a device intended to...treatment of carcinoid tumors of endocrine tissue. (b)...

  10. 21 CFR 862.1390 - 5-Hydroxyindole acetic acid/serotonin test system.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...DEVICES Clinical Chemistry Test Systems § 862.1390 5-Hydroxyindole...acetic acid/serotonin test system. (a) Identification...acetic acid/serotonin test system is a device intended to...treatment of carcinoid tumors of endocrine tissue. (b)...

  11. Mn12-acetate thin film patterns and their interaction with superconductors 

    E-print Network

    Kim, Kyongwan

    2009-05-15

    Mn12-acetate single-molecule magnets (SMMs) are nano-scale magnets showing a strong magnetic anisotropy, slow relaxation and stepwise magnetic hysteresis curves. Possible applications of Mn12-acetate, e.g. for ultra high density magnetic information...

  12. 21 CFR 524.1484d - Neomycin sulfate, hydrocortisone acetate, tetracaine hydrochloride ear ointment.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...hydrocortisone acetate, tetracaine hydrochloride ear ointment. 524.1484d Section 524...hydrocortisone acetate, tetracaine hydrochloride ear ointment. (a) Specifications...externa in dogs and cats. In treatment of ear canker and other inflammatory...

  13. 21 CFR 524.1484d - Neomycin sulfate, hydrocortisone acetate, tetracaine hydrochloride ear ointment.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...hydrocortisone acetate, tetracaine hydrochloride ear ointment. 524.1484d Section 524...hydrocortisone acetate, tetracaine hydrochloride ear ointment. (a) Specifications...externa in dogs and cats. In treatment of ear canker and other inflammatory...

  14. 21 CFR 524.1484d - Neomycin sulfate, hydrocortisone acetate, tetracaine hydrochloride ear ointment.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...hydrocortisone acetate, tetracaine hydrochloride ear ointment. 524.1484d Section 524...hydrocortisone acetate, tetracaine hydrochloride ear ointment. (a) Specifications...externa in dogs and cats. In treatment of ear canker and other inflammatory...

  15. 21 CFR 524.1484d - Neomycin sulfate, hydrocortisone acetate, tetracaine hydrochloride ear ointment.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...hydrocortisone acetate, tetracaine hydrochloride ear ointment. 524.1484d Section 524...hydrocortisone acetate, tetracaine hydrochloride ear ointment. (a) Specifications...externa in dogs and cats. In treatment of ear canker and other inflammatory...

  16. 21 CFR 524.1204 - Kanamycin sulfate, calcium amphomycin, and hydrocortisone acetate.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...2011-04-01 false Kanamycin sulfate, calcium amphomycin, and hydrocortisone acetate...524.1204 Kanamycin sulfate, calcium amphomycin, and hydrocortisone acetate. (a) Specifications. (1) Calcium amphomycin is the calcium salt...

  17. 21 CFR 177.1360 - Ethylene-vinyl acetate-vinyl alcohol copolymers.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...conditions: (a) Ethylene-vinyl acetate-vinyl alcohol copolymers are produced by the partial or complete alcoholysis or hydrolysis of those ethylene-vinyl acetate copolymers complying with § 177.1350. (1) Those copolymers containing a...

  18. 21 CFR 177.1360 - Ethylene-vinyl acetate-vinyl alcohol copolymers.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...conditions: (a) Ethylene-vinyl acetate-vinyl alcohol copolymers are produced by the partial or complete alcoholysis or hydrolysis of those ethylene-vinyl acetate copolymers complying with § 177.1350. (1) Those copolymers containing a...

  19. 21 CFR 177.1360 - Ethylene-vinyl acetate-vinyl alcohol copolymers.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...conditions: (a) Ethylene-vinyl acetate-vinyl alcohol copolymers are produced by the partial or complete alcoholysis or hydrolysis of those ethylene-vinyl acetate copolymers complying with § 177.1350. (1) Those copolymers containing a...

  20. 21 CFR 177.1360 - Ethylene-vinyl acetate-vinyl alcohol copolymers.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...conditions: (a) Ethylene-vinyl acetate-vinyl alcohol copolymers are produced by the partial or complete alcoholysis or hydrolysis of those ethylene-vinyl acetate copolymers complying with § 177.1350. (1) Those copolymers containing a...

  1. 21 CFR 177.1360 - Ethylene-vinyl acetate-vinyl alcohol copolymers.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...conditions: (a) Ethylene-vinyl acetate-vinyl alcohol copolymers are produced by the partial or complete alcoholysis or hydrolysis of those ethylene-vinyl acetate copolymers complying with § 177.1350. (1) Those copolymers containing a...

  2. Water requirements of the rayon- and acetate-fiber industry

    USGS Publications Warehouse

    Mussey, Orville Durey

    1957-01-01

    Water is required for several purposes in the manufacture of rayon and acetate fiber. These water requirements, as indicated by a survey of the water used by the plants operating in 1953, are both quantitative and qualitative. About 300 mgd (million gallons per day) of water was used in 1953 in the preparation of purified wood cellulose and cotton linters, the basic material from which the rayon and acetate fiber is made. An additional 620 mgd was used in the process of converting the cellulose to rayon and acetate fiber. The total, 920 mgd, is about 1 percent of the total estimated withdrawals of industrial water in the United States in 1953. The rayon- and acetate-fiber plants are scattered through eastern United States and generally are located in small towns or rural areas where there are abundant supplies of clean, soft water. Water use at a typical rayon-fiber plant was about 9 mgd, and at a typical acetate-fiber plant about 38 mgd. About 110 gallons of water was used to produce a pound of rayon fiber, 32 gallons per pound was process water and the remainder was used largely for cooling in connection with power production and air conditioning. For the manufacture of a pound of acetate fiber about 170 gallons of water was used. However, the field survey on which this report is based indicated a wide range in the amount of water used per pound of product. For example, in the manufacture of viscose rayon, the maximum unit water use was 8 times the minimum unit water use. Water use in summer was about 22 percent greater than average annual use. About 8 mgd Of water was consumed by evaporation in the manufacture of rayon and acetate fiber. More than 90 percent of the water used by the rayon and acetate industry was with- drawn from surface-water sources, about 8 percent from ground water, and less than 2 percent from municipal water supplies. All available analyses of the untreated waters used by the rayon and acetate industry were collected and studied. The untreated waters were generally cool, low in content of calcium and magnesium, and very low in iron and manganese. At many plants, water was obtained from more than one source, and thus had different quality characteristics. Dissolved solids in all the untreated waters analyzed ranged between 14 and 747 ppm (parts per million) but in those waters used in processing the dissolved solids content was less than 200 ppm. The cooling water used by the industry is also generally of very high quality, principally because the requirements for a high-quality process water necessitate location of the plants in areas where such water is available.

  3. Displacement-Current Generation from Spread Monolayers of Poly(vinyl alcohol)s Bearing Azobenzene Sides

    NASA Astrophysics Data System (ADS)

    Naruse, Haruhiko; Ohnishi, Koji; Iwamoto, Mitsumasa; Ichimura, Kunihiro; Seki, Takahiro; Tamaki, Takashi; Iriyama, Keiji

    1993-06-01

    Generation of displacement current across single monolayers of poly(vinyl alcohol)s bearing azobenzene sides was investigated with alternating irradiation with ultraviolet light and visible light. The displacement-current generation was accompanied by a change in the area occupied per molecule. The direction of the displacement-current generation was found to be explained by the change in the vertical component of dipole moment of monolayers perpendicular to the water surface due to the cis-trans photoisomerization.

  4. Percutaneous right portal vein embolization with polyvinyl alcohol particles in gastric cancer metastasis: report of a case.

    PubMed

    Kutlu, Ramazan; Sarac, Kaya; Yilmaz, Sezai; Kirimlioglu, Vedat; Baysal, Tamer; Alkan, Alpay; Sigirci, Ahmet

    2005-01-01

    Polyvinyl alcohol (PVA) particles are used for the embolization of various vascular tumors. They are also used before hepatic resection to embolize the ipsilateral portal vein, causing hypertrophy of the remaining liver. We report our first experience with portal vein embolization (PVE) with PVA particles to treat gastric cancer metastasis to the liver. PVE with PVA is a safe interventional radiologic procedure, which does not cause problems during surgery and can improve the outcome of hepatic resection. PMID:16133672

  5. Photoinduced crystallization of calcium carbonate from a homogeneous precursor solution in the presence of partially hydrolyzed poly(vinyl alcohol)

    NASA Astrophysics Data System (ADS)

    Nishio, Takashi; Naka, Kensuke

    2015-04-01

    Photoinduced crystallization of calcium carbonate (CaCO3) was demonstrated by the photodecarboxylation of ketoprofen (KP, 2-(3-benzoylphenyl)propionic acid) under alkaline conditions (pH 10). In this method, a homogeneous solution comprising KP, calcium chloride, ammonia, and partially hydrolyzed poly(vinyl alcohol) (PVAPS, degree of saponification: 86.5-89.0 mol %) was used as the precursor solution and was exposed to ultraviolet (UV) irradiation for different time periods. Thermogravimetric analysis of the obtained xerogels showed that increasing the UV irradiation time increased the amount of CaCO3 formed and the complete conversion of calcium ions to calcite was achieved after 50 min of UV irradiation. Furthermore, solid phase analyses suggested that nanometer-to-micron-sized calcite crystals were formed and dispersed in the obtained PVAPS matrix. Photoinduced crystallization of CaCO3 from homogenous solution was demonstrated. 2-(3-benzoylphenyl)propionic acid was used as a photoreactive CO2 generator. Partially hydrolyzed poly(vinyl alcohol) worked as a stabilizer in the solution. Complete conversion of Ca2+ to CaCO3 was achieved by UV irradiation for 50 min. Nanometer-to-micron-sized calcites dispersed in the poly(vinyl alcohol) matrix.

  6. Development of structure in natural silk spinning and poly(vinyl alcohol) hydrogel formation

    NASA Astrophysics Data System (ADS)

    Willcox, Patricia Jeanene

    This research involves the characterization of structure and structure formation in aqueous systems. Particularly, these studies investigate the effect of various processing variables on the structure formation that occurs upon conversion from aqueous solution to fiber or hydrogel. The two processes studied include natural silk fiber spinning and physical gelation of poly(vinyl alcohol), PVOH, in water. The techniques employed combine cryogenic technology for sample preparation and direct observation by transmission electron microscopy with electron diffraction, atomic force microscopy, optical rheometry, X-ray scattering and optical microscopy. In order to explore the full range of structure formation in natural silk spinning, studies are conducted in vivo and in vitro. In vivo structural investigations are accomplished through the cryogenic quenching and subsequent microtoming of live silk-spinning animals, Nephila clavipes (spider) and Bombyx mori (silkworm). Observations made using transmission electron microscopy, electron diffraction and atomic force microscopy indicate a cholesteric liquid crystalline mesophase of aqueous silk fibroin in both species. The mechanism of structure formation in solution is studied in vitro using optical rheometry on aqueous solutions made from regenerated Bombyx mori cocoon silk. Concentrated solutions exhibit birefringence under flow, with a wormlike conformation of the silk molecules in concentrated salt solution. Changes in salt concentration and pH of the aqueous silk solutions result in differing degrees of alignment and aggregation. These results suggest that structural control in the natural silk spinning process is accomplished by chemical manipulation of the electrostatic interactions and hydrogen bonding between chains. Application of cryogenic methods in transmission electron microscopy also provides a unique look at hydration-dependent structures in gels of poly(vinyl alcohol) produced by freeze-thaw processing. Morphologies ranging from circular pores to fibrillar networks are observed in gels formed from aqueous PVOH solutions subjected to cycles of freezing and thawing. These morphologies can be directly associated with the progressive nature of the mechanism of gelation as it proceeds from liquid-liquid phase separation to crystallization with increased cycling. A comparison of the structures produced by cycling and by aging suggests that there is a similarity in structural changes, but a superposition of the effects of cycling and aging is not possible.

  7. 40 CFR 721.8658 - Modified polymer of vinyl acetate and quaternary ammonium compound (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Modified polymer of vinyl acetate and... Significant New Uses for Specific Chemical Substances § 721.8658 Modified polymer of vinyl acetate and.... (1) The chemical substance identified generically as modified polymer of vinyl acetate and...

  8. 40 CFR 721.8658 - Modified polymer of vinyl acetate and quaternary ammonium compound (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Modified polymer of vinyl acetate and... Significant New Uses for Specific Chemical Substances § 721.8658 Modified polymer of vinyl acetate and.... (1) The chemical substance identified generically as modified polymer of vinyl acetate and...

  9. 40 CFR 721.8658 - Modified polymer of vinyl acetate and quaternary ammonium compound (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Modified polymer of vinyl acetate and... Significant New Uses for Specific Chemical Substances § 721.8658 Modified polymer of vinyl acetate and.... (1) The chemical substance identified generically as modified polymer of vinyl acetate and...

  10. EVALUATION OF NATURAL SOURCE VITAMIN E, RRR--TOCOPHERYL ACETATE, AS AN ALTERNATIVE MICRONUTRIENT SOURCE AND

    E-print Network

    EVALUATION OF NATURAL SOURCE VITAMIN E, RRR--TOCOPHERYL ACETATE, AS AN ALTERNATIVE MICRONUTRIENT APPROVAL EVALUATION OF NATURAL SOURCE VITAMIN E, RRR--TOCOPHERYL ACETATE, AS AN ALTERNATIVE MICRONUTRIENT: Evaluation of Natural Source Vitamin E, RRR--Tocopheryl Acetate, as an Alternative Micronutrient Source

  11. 40 CFR 180.1258 - Acetic acid; exemption from the requirement of a tolerance.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...2010-07-01 false Acetic acid; exemption from the requirement...Tolerances § 180.1258 Acetic acid; exemption from the requirement...biochemical pesticide acetic acid when used as a preservative...timothy, hay; vetch, hay; and wheat, grain, or commodities...

  12. 21 CFR 175.350 - Vinyl acetate/crotonic acid copolymer.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...2009-04-01 true Vinyl acetate/crotonic acid copolymer. 175.350 Section 175.350... § 175.350 Vinyl acetate/crotonic acid copolymer. A copolymer of vinyl acetate and crotonic acid may be safely used as a coating or...

  13. 40 CFR 721.8658 - Modified polymer of vinyl acetate and quaternary ammonium compound (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 2011-07-01 false Modified polymer of vinyl acetate and quaternary ammonium...Chemical Substances § 721.8658 Modified polymer of vinyl acetate and quaternary ammonium...substance identified generically as modified polymer of vinyl acetate and quaternary...

  14. 40 CFR 721.8658 - Modified polymer of vinyl acetate and quaternary ammonium compound (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...2010-07-01 2010-07-01 false Modified polymer of vinyl acetate and quaternary ammonium...Chemical Substances § 721.8658 Modified polymer of vinyl acetate and quaternary ammonium...substance identified generically as modified polymer of vinyl acetate and quaternary...

  15. 40 CFR 721.8658 - Modified polymer of vinyl acetate and quaternary ammonium compound (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...2013-07-01 2013-07-01 false Modified polymer of vinyl acetate and quaternary ammonium...Chemical Substances § 721.8658 Modified polymer of vinyl acetate and quaternary ammonium...substance identified generically as modified polymer of vinyl acetate and quaternary...

  16. 21 CFR 177.1360 - Ethylene-vinyl acetate-vinyl alcohol copolymers.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies may be obtained from the Office of... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ethylene-vinyl acetate-vinyl alcohol copolymers... acetate-vinyl alcohol copolymers. Ethylene-vinyl acetate-vinyl alcohol copolymers (CAS Reg. No....

  17. Gold(I)-catalyzed enantioselective [32] and [33] cycloaddition reactions of propargyl acetals/ketals

    E-print Network

    Toste, Dean

    Gold(I)-catalyzed enantioselective [3þ2] and [3þ3] cycloaddition reactions of propargyl acetals May 2015 Keywords: Gold Homogeneous catalysis Enantioselective catalysis Cycloaddition Propargyl acetals/ketals a b s t r a c t An asymmetric gold(I)-catalyzed [3þ2] cycloaddition of propargyl acetals

  18. 40 CFR 721.8658 - Modified polymer of vinyl acetate and quaternary ammonium compound (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Modified polymer of vinyl acetate and... Significant New Uses for Specific Chemical Substances § 721.8658 Modified polymer of vinyl acetate and.... (1) The chemical substance identified generically as modified polymer of vinyl acetate and...

  19. 40 CFR 721.8658 - Modified polymer of vinyl acetate and quaternary ammonium compound (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Modified polymer of vinyl acetate and... Significant New Uses for Specific Chemical Substances § 721.8658 Modified polymer of vinyl acetate and.... (1) The chemical substance identified generically as modified polymer of vinyl acetate and...

  20. SPECTROFLUOROMETRIC AND HIGH-PERFORMANCE LIQUID CHROMATOGRAPHIC DETERMINATION OF a-TOCOPHEROL ACETATE IN OLIVE OIL

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A high performance liquid chromatographic (HPLC) method was developed for the quantitative determination of '-acetate tocopherol in olive oil. After extracts in n-hexane, acetate '- tocopherol were quantitatively analyzed by HPLC with fluorimetric detector. The presence of acetate '- tocopherol in...

  1. Determination of Formic and Acetic Acid in Chondritic Meteorites

    NASA Astrophysics Data System (ADS)

    Briscoe, J. F.; Moore, C. B.

    1993-07-01

    The concentrations of formic and acetic acid have been determined using ion exclusion chromatography after water extraction from several chondritic meteorite samples. Monocarboxylic acids are of great importance because of their high concentration in meteorites and for their role as precursor molecules in organic synthesis [1]. The concentration of acetic acid has been determined previously using gas chromatography [2,3]. Prior gas chromatographic analyses failed to resolve formic acid and so the results were limited to carboxylic acids having two or more carbons. Alternatively, wet chemical methods for the determination of formic acid, although precise, are lengthy and difficult to reproduce [4]. Ion exclusion chromatography (ICE) is an excellent technique for the simultaneous determination of formic and acetic acids. Using ICE the carboxylic acids can be determined in less time and with minimal sample handling. In most cases the amount of formic acid present is found to be lower than the amount of acetic acid present. This contradicts the accepted synthesis scheme of higher homologs being made from lower members, where the formic acid would be expected to have a higher concentration than acetic acid. Other monocarboxylic acids in the homologous series (C(sub)2-C(sub)7) have been shown to decrease with increasing carbon number as expected [2,3]. This data suggests that either the formic acid may have been preferentially depleted or it may have a different synthesis mechanism as compared with the other monocarboxylic acids present in meteorites. Additionally, there is a relationship between the amount of formic and acetic acid present and the oxidation state of the iron in the chondrites. As the matrix environment becomes more oxidizing, the amount of the two monocarboxylic acids increases comparatively. Furthermore, the ratio of formic to acetic acid starts to increase as the metal phase is more oxidized, suggesting that a more oxidized matrix environment in some way makes the production of higher homologs from lower members more favorable. References: [1] Cronin J. R. et al. (1988) In Meteorites and the Early Solar System (J. F. Kerridge and M. S. Matthews, eds.), 819-857. Univ. of Arizona. [2] Yuen G. U. and Kvenvolden K. A. (1974) Nature, 246, 301-303. [3] Yuen G. et al. (1984) Nature, 307, 252-254. [4] Kimball B. (1988) M.S. thesis, Arizona State Univ. [5] Urey H. C. and Craig H. (1953) GCA, 4, 36-82. [6] Sears D. W. and Dodd R. T. (1988) In Meteorites and the Early Solar System (J. F. Kerridge and M. S. Matthews, eds.), 3-31. Univ. of Arizona. Table 1, which appears here in the hard copy, shows a representative concentration of formic and acetic acid (in ppm) for select chondrites as measured by ion exclusion chromatography.

  2. Isothermal decomposition of gamma-irradiated dysprosium acetate

    NASA Astrophysics Data System (ADS)

    Mahfouz, R. M.; Al-Shehri, S. M.; Monshi, M. A. S.; Abd El-Salam, N. M.

    Isothermal decomposition of un-irradiated and pre-gamma-irradiated dysprosium acetate [Dy(CH3COO)(3)] has been investigated at different temperatures between 603-623 K. Irradiation was observed to enhance the rate of decomposition without modifying the mechanism of the thermal decomposition. Thermal decomposition of dysposium acetate is shown to proceed by a nucleation and growth mechanism (Avarmi-Erofe'ev equation) both for un-irradiated and pre-gamma-irradiated samples. The enhancement of the decomposition was found to increase with an increase in the gamma-ray dose applied to the sample and may be attributed to an increase in point defects and formation of additional nucleation centers generated in the host lattice. Thermodynamic values of the main decomposition process were calculated and evaluated.

  3. Digestive stability of hydroxytyrosol, hydroxytyrosyl acetate and alkyl hydroxytyrosyl ethers.

    PubMed

    Pereira-Caro, Gema; Sarriá, Beatriz; Madrona, Andrés; Espartero, José Luis; Escuderos, María E; Bravo, Laura; Mateos, Raquel

    2012-09-01

    The digestive stability of two natural antioxidant compounds present in virgin olive oil, hydroxytyrosol (HTy) and hydroxytyrosyl acetate (HTy-Ac) and a new series of hydroxytyrosyl ethers (methyl, ethyl and butyl hydroxytyrosyl ethers) was evaluated by a simulated digestion procedure. High recovery of all compounds after gastric digestion was obtained, although they showed a statistically significant lower stability after pancreatic-bile salts digestion. HTy-Ac was partially hydrolyzed into free HTy, whereas after intestinal digestion, HTy was converted into 3,4-dihydroxyphenyl acetic acid (DOPAC), and HTy-Ac was hydrolyzed to HTy and subsequently transformed into DOPAC. In contrast, no chemical modification of hydroxytyrosyl ethers during in vitro digestion was observed. In summary, HTy, HTy-Ac and hydroxytyrosyl ethers show high and interesting digestive stability and the new synthetic hydroxytyrosyl ethers showed enhanced chemical stability compared to HTy and HTy-Ac. PMID:22268563

  4. Evaluation of lanthanide salts as alternative stains to uranyl acetate.

    PubMed

    Hosogi, Naoki; Nishioka, Hideo; Nakakoshi, Masamichi

    2015-12-01

    Uranyl acetate (UAc) has been generally used not only as a superb staining reagent for ultrathin sections of plastic-embedded biological materials, but also as high-contrast negative stains for biological macromolecules such as particles of protein or virus. However, the use and purchase of radioactive UAc have been restricted. In this study, we determine the performance of ytterbium triacetate, lutetium triacetate, samarium triacetate and gadolinium triacetate as new staining reagents for biological electron microscopy. We observed chemically fixed spinach (Spinacia oleracea) leaves stained with these reagents. Ultrathin sections were stained with these reagents. Some of them were counterstained with lead citrate. The transmission electron microscopy contrast of spinach organelles was evaluated in sections exposed to the conventional stain and new stains. We show acetate salts of samarium, gadolinium, ytterbium and lutetium could be excellent substitutes for UAc for thin section staining and for negative staining. In addition, each reagent showed appreciable negative-staining effects. PMID:26374081

  5. Synthesis and Decarboxylative Coupling of Sulfonyl Acetic Esters

    E-print Network

    Weaver, Jimmie Dean

    2010-04-28

    make the reaction more tolerant of both ?-H’s and ?-H’s on the allyl component, cyclohex-2-enyl 2-phenyl-2-(phenylsulfonyl)acetate was synthesized. The substrate was first subjected to the standard conditions which required some heating but gave.... In addition to not reaching completion the amount of protonation product increased significantly. The incomplete reaction might be explained if the phosphine ligand is the reductant. If the BINAP ligand is oxidized, it would likely not ligate comparably...

  6. Kinetic model of acetate metabolism in healthy and hyperinsulinaemic humans

    PubMed Central

    Fernandes, Judlyn; Vogt, Janet; Wolever, Thomas MS

    2014-01-01

    Background/objectives The short chain fatty acid acetate (AC), may play a role in increasing insulin sensitivity, thus lowering risk for obesity and type 2 diabetes mellitus. It is unclear if AC kinetics is similar in normal and hyperinsulinaemic participants. Therefore, we studied AC absorption from the distal colon in participants with normal (<40 pmol/L, NI) and high (?40 pmol/L, HI) plasma-insulin. This work was part of a series of studies conceived to compute a kinetic model for acetate. Kinetic parameters such as estimates of rate of entry into peripheral blood, hepatic uptake and endogenous/exogenous production were compared in the groups. Subjects/methods Overnight fasted NI (n = 9) and HI (n = 8) participants were given rectal infusions containing sodium acetate (90 mmol/L). The solutions were retained for 40 min, then voided for AC measurement. Total amount of AC infused was 27 mmols. Results Acetate absorption from the distal colon (279±103 vs 322±91 ?mol/min, P = 0.76) and hepatic uptake of AC (155±101 vs 146±85 ?mol/min, P = 0.94) were similar in the groups. Endogenous and exogenous AC production was significantly higher in NI than HI participants. Plasma AC was inversely proportional to plasma insulin concentrations in the entire cohort (y=k/x, where k = 1813). Conclusions There was low power to detect differences in AC absorption rate and hepatic AC uptake in NI vs HI. The rate of entry of AC into peripheral blood was similar in NI and HI participants. However, hyperinsulinaemia may alter endogenous and exogenous AC metabolism. PMID:25052228

  7. Acetic acid bacteria spoilage of bottled red wine -- a review.

    PubMed

    Bartowsky, Eveline J; Henschke, Paul A

    2008-06-30

    Acetic acid bacteria (AAB) are ubiquitous organisms that are well adapted to sugar and ethanol rich environments. This family of Gram-positive bacteria are well known for their ability to produce acetic acid, the main constituent in vinegar. The oxidation of ethanol through acetaldehyde to acetic acid is well understood and characterised. AAB form part of the complex natural microbial flora of grapes and wine, however their presence is less desirable than the lactic acid bacteria and yeast. Even though AAB were described by Pasteur in the 1850s, wine associated AAB are still difficult to cultivate on artificial laboratory media and until more recently, their taxonomy has not been well characterised. Wine is at most risk of spoilage during production and the presence of these strictly aerobic bacteria in grape must and during wine maturation can be controlled by eliminating, or at least limiting oxygen, an essential growth factor. However, a new risk, spoilage of wine by AAB after packaging, has only recently been reported. As wine is not always sterile filtered prior to bottling, especially red wine, it often has a small resident bacterial population (<10(3) cfu/mL), which under conducive conditions might proliferate. Bottled red wines, sealed with natural cork closures, and stored in a vertical upright position may develop spoilage by acetic acid bacteria. This spoilage is evident as a distinct deposit of bacterial biofilm in the neck of the bottle at the interface of the wine and the headspace of air, and is accompanied with vinegar, sherry, bruised apple, nutty, and solvent like off-aromas, depending on the degree of spoilage. This review focuses on the wine associated AAB species, the aroma and flavour changes in wine due to AAB metabolism, discusses the importance of oxygen ingress into the bottle and presents a hypothesis for the mechanism of spoilage of bottled red wine. PMID:18237809

  8. Propagation of avalanches in Mn12-acetate: magnetic deflagration.

    PubMed

    Suzuki, Yoko; Sarachik, M P; Chudnovsky, E M; McHugh, S; Gonzalez-Rubio, R; Avraham, Nurit; Myasoedov, Y; Zeldov, E; Shtrikman, H; Chakov, N E; Christou, G

    2005-09-30

    Local time-resolved measurements of fast reversal of the magnetization of single crystals of Mn12-acetate indicate that the magnetization avalanche spreads as a narrow interface that propagates through the crystal at a constant velocity that is roughly 2 orders of magnitude smaller than the speed of sound. We argue that this phenomenon is closely analogous to the propagation of a flame front (deflagration) through a flammable chemical substance. PMID:16241690

  9. Degradation of vinyl acetate by soil, sewage, sludge, and the newly isolated aerobic bacterium V2.

    PubMed Central

    Nieder, M; Sunarko, B; Meyer, O

    1990-01-01

    Vinyl acetate is subject to microbial degradation in the environment and by pure cultures. It was hydrolyzed by samples of soil, sludge, and sewage at rates of up to 6.38 and 1 mmol/h per g (dry weight) under aerobic and anaerobic conditions, respectively. Four yeasts and thirteen bacteria that feed aerobically on vinyl acetate were isolated. The pathway of vinyl acetate degradation was studied in bacterium V2. Vinyl acetate was degraded to acetate as follows: vinyl acetate + NAD(P)+----2 acetate + NAD(P)H + H+. The acetate was then converted to acetyl coenzyme A and oxidized through the tricarboxylic acid cycle and the glyoxylate bypass. The key enzyme of the pathway is vinyl acetate esterase, which hydrolyzed the ester to acetate and vinyl alcohol. The latter isomerized spontaneously to acetaldehyde and was then converted to acetate. The acetaldehyde was disproportionated into ethanol and acetate. The enzymes involved in the metabolism of vinyl acetate were studied in extracts. Vinyl acetate esterase (Km = 6.13 mM) was also active with indoxyl acetate (Km = 0.98 mM), providing the basis for a convenient spectrophotometric test. Substrates of aldehyde dehydrogenase were formaldehyde, acetaldehyde, propionaldehyde, and butyraldehyde. The enzyme was equally active with NAD+ or NADP+. Alcohol dehydrogenase was active with ethanol (Km = 0.24 mM), 1-propanol (Km = 0.34 mM), and 1-butanol (Km = 0.16 mM) and was linked to NAD+. The molecular sizes of aldehyde dehydrogenase and alcohol dehydrogenase were 145 and 215 kilodaltons, respectively. PMID:2285314

  10. Ethylene-Vinyl Acetate Potential Problems for Photovoltaic Packaging: Preprint

    SciTech Connect

    Kempe, M. D.; Jorgensen, G. J.; Terwilliger, K. M.; McMahon, T. J.; Kennedy, C. E.; Borek, T. T.

    2006-05-01

    Photovoltaic (PV) devices are typically encapsulated using ethylene-vinyl acetate (EVA) to provide mechanical support, optical coupling, electrical isolation, and protection against environmental exposure. Under exposure to atmospheric water and/or ultraviolet radiation, EVA will decompose to produce acetic acid, lowering the pH and increasing the surface corrosion rates of embedded devices. Even though acetic acid is produced at a very slow rate, it may not take much to catalyze reactions that lead to rapid module deterioration. Another consideration is that the glass transition of EVA, as measured using dynamic mechanical analysis, begins at temperatures of about ?15 C. Temperatures lower than this can be reached for extended periods of time in some climates. Because of increased moduli below the glass transition temperature, a module may be more vulnerable to damage if a mechanical load is applied by snow or wind at low temperatures. Modules using EVA should not be rated for use at such low temperatures without additional low-temperature mechanical testing beyond the scope of UL 1703.

  11. Miscibility and dynamical properties of cellulose acetate/plasticizer systems.

    PubMed

    Bao, Cong Yu; Long, Didier R; Vergelati, Caroll

    2015-02-13

    Due to its biodegradability and renewability, a great interest has been devoted to investigating cellulose acetate in order to expand its potential applications. In addition, secondary cellulose acetate (CDA) could also be considered as a model system for strongly polar polymer system. The dynamical behavior of CDA is supposed to be governed by H-bonding and dipolar interaction network. Due to their high glass transition temperature, cellulose acetate-based systems are processed when blended with plasticizers. It is thus of utmost importance to study the miscibility and plasticizing effects of various molecules. We prepared CDA films via solvent casting method with diethyl phthalate as the plasticizer. Miscibility diagrams were established by calorimetry and thermo-mechanical (DMTA) experiments. Dynamical properties were analyzed by DMTA and broadband dielectric spectroscopy. We could identify the ?-relaxation of these CDA-plasticizer systems in the frequency range from 0.06 Hz to 10(6)Hz, which allowed for describing the dynamics in the so-called Williams-Landel-Ferry/Vogel-Fulcher-Tammann regime. PMID:25458277

  12. Enzyme immunoassay for nomegestrol acetate in human plasma.

    PubMed

    Ezan, E; Benech, H; Bucourt, R; Ardouin, T; Tchernatinsky, C; Thomas, J L; Paris, J; Grognet, J M

    1993-10-01

    Currently available chromatographic assays of the progestative drug nomegestrol acetate in human plasma are not suitable for monitoring drug kinetics more than 24 h after clinical dosage. A specific and sensitive enzyme immunoassay was therefore developed. A 3(O-carboxymethyl)oxime derivative of nomegestrol acetate was synthesized and coupled to bovine serum albumin in order to raise polyclonal antibodies in rabbits. The enzymatic tracer was obtained by coupling the 3(O-carboxymethyl)oxime derivative to acetylcholinesterase (E.C.3.1.1.7.). HPLC fractionation of human plasma samples followed by enzyme immunoassay revealed the presence of cross-reacting metabolites. An automated procedure of metabolite separation was developed using silica bonded with diol groups (Diol Bakerbond column). This procedure ensured assay specificity. The quantification limit in human plasma was 0.1 ng/ml. Mean repeatability (intra-assay variation) and reproducibility (inter-assay variation) were 9 and 15%, respectively. The enzyme immunoassay allowed monitoring of the kinetics of nomegestrol acetate 144 h after oral administration of a single 5 mg dose. Values for human samples were in excellent agreement with those assayable by HPLC followed by u.v. detection. PMID:8217881

  13. In-Line Ultrasonic Monitoring for Sediments Stuck on Inner Wall of a Polyvinyl Chloride Pipe

    PubMed Central

    2014-01-01

    This research verified the applicability and effectiveness of the ultrasonic monitoring of sediments stuck on the inner wall of polyvinyl chloride (PVC) pipes. For identifying the transmittance of acoustic energy and the speed of sound in the PVC material, the pulse-echo ultrasonic testing was conducted for PVC sheets of different thicknesses. To simulate the solidified sediment, the hot melt adhesive (HMA) was covered on the inner wall of the PVC pipe in different heights. From the experiment, the speeds of sound in the PVC and the HMA materials were obtained as about 2258 and 2000?m/s, respectively. The thickness of the materials was calculated through the signal processing such as taking the absolute value and low pass filtering, the echo detection, and the measurement of the time of flight. The errors between actual and measured thicknesses of PVC sheets were below 5%. In the case of the substance stuck on the inner wall, the errors were below 2.5%. Since the pulse-echo ultrasonic inspection is available on the outer surface and its measurement accuracy was over 95%, it can be an efficient and effective in-service structural health monitoring for the sediment on the wall of PVC pipes. PMID:25243223

  14. Nonlinear optical characterization of the Ag nanoparticles doped in polyvinyl alcohol films

    NASA Astrophysics Data System (ADS)

    Ghanipour, Mahshad; Dorranian, Davoud

    2015-06-01

    The effect of silver nanoparticles doped in polyvinyl alcohol (PVA) on the nonlinear optical properties of composite films is studied experimentally. Samples are PVA films of 0.14 mm thickness doped with different concentrations of silver nanoparticles. Nonlinear optical properties of doped polymer films are studied experimentally employing Z-scan techniques. Experiments are performed using the second harmonic of a continuous Nd-Yag laser beam at 532 nm wavelength and 45 mW power. The effect of nonlinear refractive index of samples is obtained by measuring the profile of propagated beam through the samples and their nonlinear refractive index is found to be negative. The nonlinear absorption coefficient is calculated using open aperture Z-scan data while its nonlinear refractive index is measured using the closed aperture Z-scan data, leads to measuring the third order susceptibility |?(3)|. Real and imaginary parts of the third-order nonlinear optical susceptibility |?(3)| are decrease with increasing the concentration of Ag nanoparticles in the films. The values of thermo-optic coefficient are determined at different concentrations of silver nanoparticles for samples.

  15. Enlarged-taper tailored Fiber Bragg grating with polyvinyl alcohol coating for humidity sensing

    NASA Astrophysics Data System (ADS)

    Liang, Yanhong; Yan, Guofeng; He, Sailing

    2015-08-01

    In this paper, a novel optical fiber sensor based on an enlarged-taper tailored fiber Bragg grating (FBG) is proposed and experimentally demonstrated for the measurement of relative humidity. The enlarged-taper works as a multifunctional joint that not only excites cladding modes but also recouples the cladding modes reflected by the FBG back into the leading single mode fiber. Due to the fact that cladding modes have a strong evanescent field penetrating into the ambient medium, the intensity of the reflected cladding modes is greatly influenced by the refractive index (RI) of the ambient medium. Polyvinyl alcohol (PVA) film is plated on the fiber surface by dip-coating technique, as a humidity-to-refractive index transducer, whose RI variance from 1.49 to 1.34 when the ambient humidity increases from 20%RH to 95%RH. The relative humidity response of the sensing structure is investigated in our home-made humidity chamber with a commercial hygrometer. By monitoring the intensity of the reflected cladding modes, the RH variance can be demodulated. Experimental results show that RH sensitivity depends on the RH value, and a sensitivity up to 1.2 dB/%RH can be achieved within the RH range of 30-90%. A fast and reversible time response has also been investigated. Such a probe-type and reusable fiber-optic RH sensor is a very promising technology for biochemical sensing applications, e.g., breath analysis, chemical reaction monitoring.

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

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

    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 SiO2/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.

  17. Influence of water content on structure and mobility of polyvinyl alcohol: a molecular dynamics simulation.

    PubMed

    Sacristan Bermejo, Javier; Mijangos Ugarte, Carmen

    2008-10-21

    Fully atomistic molecular dynamics simulations have been performed on aqueous solutions of polyvinyl alcohol (PVA) to get some insight into the effect of water content on PVA structure and dynamics. Simulations were carried out on mixtures of water/atactic PVA at 300 K covering a composition range (water weight fraction X(w)=0.1-0.8. The analysis focuses on polymer segmental dynamics, which is monitored by the mean square displacement, Van Hove self correlation function, non-Gaussian parameter, and the intermediate incoherent scattering function. It was found that PVA dynamics is strongly affected by addition of water. Both, PVA carbon and hydrogen (hydroxyl and main chain hydrogens) motions are faster with further dilution. Differences on atom mobility (dynamic heterogeneity) decreases as water content increases allowing more isotropic segmental motions. Moreover, the non-Gaussian parameter shows a maximum at X(w)=0.25 followed by a continuous decrease with dilution. The non-Gaussian effects become more important as the water content decreases and dynamic heterogeneity is enhanced. These results are explained in terms of the plasticization effects of water on the polymer and the intrinsic dynamic heterogeneity observed on PVA dynamics. PMID:19045229

  18. Influence of water content on structure and mobility of polyvinyl alcohol: A molecular dynamics simulation

    NASA Astrophysics Data System (ADS)

    Bermejo, Javier Sacristan; Ugarte, Carmen Mijangos

    2008-10-01

    Fully atomistic molecular dynamics simulations have been performed on aqueous solutions of polyvinyl alcohol (PVA) to get some insight into the effect of water content on PVA structure and dynamics. Simulations were carried out on mixtures of water/atactic PVA at 300 K covering a composition range (water weight fraction Xw=0.1-0.8. The analysis focuses on polymer segmental dynamics, which is monitored by the mean square displacement, Van Hove self correlation function, non-Gaussian parameter, and the intermediate incoherent scattering function. It was found that PVA dynamics is strongly affected by addition of water. Both, PVA carbon and hydrogen (hydroxyl and main chain hydrogens) motions are faster with further dilution. Differences on atom mobility (dynamic heterogeneity) decreases as water content increases allowing more isotropic segmental motions. Moreover, the non-Gaussian parameter shows a maximum at Xw=0.25 followed by a continuous decrease with dilution. The non-Gaussian effects become more important as the water content decreases and dynamic heterogeneity is enhanced. These results are explained in terms of the plasticization effects of water on the polymer and the intrinsic dynamic heterogeneity observed on PVA dynamics

  19. Polyvinylpyrrolidone/polyvinyl butyral composite as a stable binder for castable supercapacitor electrodes in aqueous electrolytes

    NASA Astrophysics Data System (ADS)

    Aslan, M.; Weingarth, D.; Herbeck-Engel, P.; Grobelsek, I.; Presser, V.

    2015-04-01

    Mixtures of polyvinylpyrrolidone/polyvinyl butyral (PVP/PVB) are attractive binders for the preparation of carbon electrodes for aqueous electrolyte supercapacitors. The use of PVP/PVB offers several key advantages: They are soluble in ethanol and can be used to spray coat or drain cast activated carbon (AC) electrodes directly on a current collector. Infrared spectroscopy and contact angle measurements show that the PVP-to-PVB ratio determines the degree of binder hydrophilicity. Within our study, the most favorable performance was obtained for AC electrodes with a composition of AC + 1.5 mass% PVP + 6.0 mass% PVB; such electrodes were mechanically stabile and water resistant with a PVP release of less than 5% of total PVP while PVB itself is water insoluble. Compared to when using PVDF, the specific surface area (SSA) of the assembled electrodes was 10% higher, indicating a reduced pore blocking tendency. A good electrochemical performance was observed in different aqueous electrolytes for composite electrodes with the optimized binder composition: 160 F g-1 at 1 A g-1 for 1 M H2SO4 and 6 M KOH and 120 F g-1 for 1 M NaCl. The capacitance was slightly reduced by 2.5% after cycling to 1.2 V with 1.28 A g-1 in 1 M NaCl for 10,000 times.

  20. Improvement of Starch Digestion Using ?-Amylase Entrapped in Pectin-Polyvinyl Alcohol Blend

    PubMed Central

    Cruz, Maurício; Fernandes, Kátia; Cysneiros, Cristine; Nassar, Reginaldo; Caramori, Samantha

    2015-01-01

    Polyvinyl alcohol (PVA) and pectin blends were used to entrap ?-amylase (Termamyl) using glutaraldehyde as a cross-linker. The effect of glutaraldehyde concentration (0.25, 0.5, 0.75, 1.0, and 1.25%) on the activity of the immobilized enzyme and rate of enzyme released was tested during a 24?h period. Characteristics of the material, such as scanning electron microscopy (SEM), tensile strength (TS), elongation, and rate of dissolution in water (pH 5.7), ruminal buffering solution (pH 7.0), and reactor containing 0.1?mol?L?1 sodium phosphate buffer (pH 6.5), were also analyzed. SEM results showed that the surfaces of the pectin/PVA/amylase films were highly irregular and rough. TS values increased as a function of glutaraldehyde concentration, whereas percentage of elongation (%E) decreased. Pectin/PVA/amylase films presented similar values of solubility in the tested solvents. The material obtained with 0.25% glutaraldehyde performed best with repeated use (active for 24?h), in a phosphate buffer reactor. By contrast, the material obtained with 1.25% glutaraldehyde presented higher performance during in vitro testing using an artificial rumen. The results suggest that pectin/PVA/amylase is a highly promising material for biotechnological applications. PMID:25949991

  1. A Study of Specific Heat Capacity Functions of Polyvinyl Alcohol- Cassava Starch Blends

    NASA Astrophysics Data System (ADS)

    Sin, Lee Tin; Rahman, W. A. W. A.; Rahmat, A. R.; Morad, N. A.; Salleh, M. S. N.

    2010-03-01

    The specific heat capacity ( C sp) of polyvinyl alcohol (PVOH) blends with cassava starch (CSS) was studied by the differential scanning calorimetry method. Specimens of PVOH-CSS blends: PPV37 (70 mass% CSS) and PPV46 (60 mass% CSS) were prepared by a melt blending method with glycerol added as a plasticizer. The results showed that the specific heat capacity of PPV37 and PPV46 at temperatures from 330 K to 530 K increased from (2.963 to 14.995) J· g-1 · K-1 and (2.517 to 14.727) J · g-1· K-1, respectively. The specific heat capacity of PVOH-CSS depends on the amount of starch. The specific heat capacity of the specimens can be approximated by polynomial equations with a curve fitting regression > 0.992. For instance, the specific heat capacity (in J · g-1 · K-1) of PPV37 can be expressed by C sp = -17.824 + 0.063 T and PPV46 by C sp = -18.047 + 0.061 T, where T is the temperature (in K).

  2. Case report of occupational asthma induced by polyvinyl chloride and nickel.

    PubMed

    Song, Ga-Won; Ban, Ga-Young; Nam, Young-Hee; Park, Hae-Sim; Ye, Young-Min

    2013-10-01

    Polyvinyl chloride (PVC) is a widely used chemical for production of plastics. However occupational asthma (OA) caused by PVC has been reported only rarely. We report a 34-yr-old male wallpaper factory worker with OA due to PVC and nickel (Ni) whose job was mixing PVC with plasticizers. He visited the emergency room due to an asthma attack with moderate airflow obstruction and markedly increased sputum eosinophil numbers. A methacholine challenge test was positive (PC20 2.5 mg/mL). Bronchoprovocation tests with both PVC and Ni showed early and late asthmatic responses, respectively. Moreover, the fractional concentration of exhaled nitric oxide (FeNO) was increased after challenge with PVC. To our knowledge, this is the first case of OA in Korea induced by exposure to both PVC and Ni. We suggest that eosinophilic inflammation may be involved in the pathogenesis of PVC-induced OA and that FeNO monitoring can be used for its diagnosis. PMID:24133363

  3. Surface properties of UV-irradiated poly(vinyl alcohol) films containing small amount of collagen

    NASA Astrophysics Data System (ADS)

    Sionkowska, Alina; P?anecka, Anna; Koz?owska, Justyna; Skopi?ska-Wi?niewska, Joanna

    2009-01-01

    The surface properties of poly(vinyl alcohol) (PVA) films in the presence of 1%, 3% and 5% of collagen before and after UV-irradiation have been studied by atomic force microscopy (AFM) and by contact angle measurements. PVA films have been obtained by solvent evaporation from water solution of PVA and PVA containing small amount of collagen. After drying, the samples were irradiated with UV light wavelength ? = 254 nm in air. Surface properties before and after UV-irradiation were observed using AFM. Contact angles of two liquids: diiodomethane (D) and glycerol (G) on polymeric films were measured at constant temperature using goniometer. The results have shown that the contact angle and the surface free energy for PVA films were altered by UV-irradiation. These alterations indicate photooxidation and an increase of polarity of the surface. The comparison of surface properties of PVA films and PVA containing collagen points out that collagen is more sensitive to photooxidation than PVA and PVA/collagen blends. PVA films containing collagen easier undergo photooxidation process with formation of new polar groups than pure PVA films.

  4. Shock pressure measurements in Polyvinyl alcohol (PVA) films using multi-frame optical shadowgraphy

    NASA Astrophysics Data System (ADS)

    Chaurasia, S.; Tripathi, S.; Leshma, P.; Pasley, J.; Kumar, M.

    2012-07-01

    The knowledge of the equation of state (EOS) of materials at high pressures in excess of 10 Mbar is important in several branches of physics including astrophysics and inertial confinement fusion. It is possible to access this high pressure regime in the laboratory using shock waves launched by the interaction of a high power laser with a solid target. To study laser driven shock waves in plastic (Polyvinyl alcohol) (C2H4O)n targets, a multiframe optical shadowgraphy technique has been developed, with spatial and temporal resolution of 12 ?m and 500 ps respectively. The experiments were performed using the 1064 nm 20 J /500 ps Nd: Glass laser at BARC. The focused laser intensity on target was varied between 6 × 1013 W/cm2 and 2.7 × 1014 W/cm2. The experimental data have been compared with the results of previous experimental and theoretical studies. The results are also found to be in agreement with SESAME data. The maximum pressure attained in the experiments was 30 Mbar, achieved with a laser intensity of 2.7 × 1014 W/cm2.

  5. Fluorescence of N,N'-dimethylaminobenzonitrile in polyvinyl alcohol stretched films

    NASA Astrophysics Data System (ADS)

    Roznowska, A.; Tomin, V. I.; Fisz, J.; Hubisz, K.

    2012-04-01

    We have demonstrated that the conditions of the charge-transfer (CT) reaction in the N,N'-dimethylaminobenzonitrile (DMABN) molecule in polyvinyl alcohol (PVA) polymer matrices can be considerably changed upon their stretching deformation. The fluorescence spectrum of DMABN in PVA has two characteristic bands in the ultraviolet (UV) and visible spectral ranges, which indicates that a CT reaction proceeds in the excited state. Stretching leads to a strong decrease in the intensity of the UV band, the contribution of which in undeformed samples is comparable with the emission in the violet range. Even single stretching PVA films strongly reduces the emission intensity of the UV band, with this effect being dramatically enhanced upon sixfold stretching. In the latter case, The fluorescence spectrum is characterized by a strong CT band, the relative intensity of which is 3.5 times higher than even in a strongly polar aprotic solvent, such as acetonitrile. The obtained data indicate that, as a result of mechanical stretching, it becomes possible to change basic intermolecular factors that affect the CT rate in PVA samples.

  6. Kinetic investigations of thermal degradation of poly(vinyl butyral) using TG/FT-IR

    NASA Astrophysics Data System (ADS)

    Liau, Leo Chau-Kuang

    Mechanism of poly(vinyl butyral) (PVB) thermal degradation in different environments were investigated based on a proposed analytical algorithm. The evolved gaseous products of PVB thermal degradation and reaction pathways were identified and constructed by GC/MS measurements. Kinetic models of PVB thermal degradation with or without ceramics were determined on the basis of weight loss and evolved gas analysis (EGA) by thermogravimetry (TG) and Fourier transform infrared spectroscopy (FT-IR) measurements. A spectral resolution method was proposed to resolve the evolved gaseous IR spectra into each constituent species spectra on a dynamic basis. The dynamic resolved spectra of each evolved species were used to construct kinetic models of PVB degradation in different environments. The models associated with Arrhenius equation were elucidated as first order parallel reactions for each volatile product. The kinetic parameters of PVB thermal degradation in the proposed mechanisms were determined. The kinetic results using isothermal and nonisothermal approaches showed excellent agreement. Activation energies of PVB thermal degradation are ˜300 in nitrogen and ˜200 in air for pure PVB, and ˜100 KJ/mole for PVB with oxide (Alsb2Osb3) or nonoxide (AlN) ceramics in nitrogen. The Polymer residues were subjected to DRIFTS technique and Leco Analyzer.

  7. Polyvinyl alcohol electrospun nanofibers containing Ag nanoparticles used as sensors for the detection of biogenic amines

    NASA Astrophysics Data System (ADS)

    Marega, Carla; Maculan, Jenny; Rizzi, Gian Andrea; Saini, Roberta; Cavaliere, Emanuele; Gavioli, Luca; Cattelan, Mattia; Giallongo, Giuseppe; Marigo, Antonio; Granozzi, Gaetano

    2015-02-01

    Polyvinyl alcohol (PVA) electrospun nanofibers containing Ag nanoparticles (NPs) have been deposited on glass substrates. The aim of the work was to test the feasibility of this approach for the detection of biogenic amines by using either the Ag localized surface plasmon resonance quenching caused by the adsorption of amines on Ag NPs or by detecting the amines by surface enhanced Raman spectroscopy (SERS) after adsorption, from the gas phase, on the metal NPs. Two different approaches have been adopted. In the first one an ethanol/water solution containing AgNO3 was used directly in the electrospinning apparatus. In this way, a simple heat treatment of the nanofibers mat was sufficient to obtain the formation of Ag NPs inside the nanofibers and a partial cross-link of PVA. In the second procedure, the Ag NPs were deposited on PVA nanofibers by using the supersonic cluster beam deposition method, so that a beam of pure Ag NPs of controlled size was obtained. Exposure of the PVA mat to the beam produced a uniform distribution of the NPs on the nanofibers surface. Ethylendiamine vapors and volatile amines released from fresh shrimp meat were chemisorbed on the nanofibers mats. A SERS spectrum characterized by a diagnostic Ag-N stretching vibration at 230 cm-1 was obtained. The results allow to compare the two different approaches in the detection of ammines.

  8. Immobilization of hydrocarbon-oxidizing bacteria in poly(vinyl alcohol) cryogels hydrophobized using a biosurfactant.

    PubMed

    Kuyukina, Maria S; Ivshina, Irena B; Gavrin, Alexander Yu; Podorozhko, Elena A; Lozinsky, Vladimir I; Jeffree, Chris E; Philp, James C

    2006-06-01

    A simple biosurfactant-based hydrophobization procedure for poly(vinyl alcohol) (PVA) cryogels was developed allowing effective immobilization of hydrocarbon-oxidizing bacteria. The resulting partially hydrophobized PVA cryogel granules (granule volume 5 microl) contained sufficient number (6.5 x 10(3)) of viable bacterial cells per granule, possessed high mechanical strength and spontaneously located at the interface in water-hydrocarbon system. Such interfacial location of PVA granules allowed high contact of immobilized biocatalyst with hydrophobic substrate and water phase, thus providing bacterial cells with mineral and organic nutrients. As a result, n-hexadecane oxidation efficiency of 51% after 10-day incubation was achieved using immobilized biocatalyst. PVA cryogels with increased hydrophobicity can be used for immobilization of bacterial cultures performing oxidative transformations of water-immiscible organic compounds. Immobilization of in situ biosurfactant producing Rhodococcus bacteria into PVA cryogel is discussed. PVA cryogel granules with entrapped alkanotrophic rhodococcal cells were stable after 10-month storage at room temperature. PMID:16316701

  9. Electrospun polyvinyl alcohol/carbon dioxide modified polyethyleneimine composite nanofiber scaffolds.

    PubMed

    Wu, Han-Bing; Bremner, David H; Nie, Hua-Li; Quan, Jing; Zhu, Li-Min

    2015-05-01

    A novel biocompatible polyvinyl alcohol/carbon dioxide modified polyethyleneimine (PVA/PEI-CO2) composite nanofiber was fabricated by a green and facile protocol, which reduces the cytotoxicity of PEI through the surface modification of the PEI with CO2. The (13)C NMR spectrum, elemental analysis, and TGA show that CO2 has been incorporated in the PEI surface resulting in a relatively stable structure. The resulting PVA/PEI-CO2 composite nanofibers have been characterized by attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), contact angle, and scanning electron microscopy (SEM). The results show that the average diameters of the nanofibers range from 265 ± 53 nm to 423 ± 80 nm. The cytotoxicity of PVA/PEI-CO2 composite nanofibers was assessed by cytotoxicity evaluation using the growth and cell proliferation of normal mice Schwann cells. SEM and the MTT assay demonstrated the promotion of cell growth and proliferation on the PVA/PEI-CO2 composite scaffold. It suggests that PEI-CO2 can have tremendous potential applications in biological material research. PMID:25540321

  10. Formation and fluidity measurement of supported lipid bilayer on polyvinyl chloride membrane

    SciTech Connect

    Kobayashi, Takuji Kono, Akiteru Sawada, Kazuaki; Futagawa, Masato; Tero, Ryugo

    2014-02-20

    We prepared an artificial lipid bilayer on a plasticized poly(vinyl chloride) (PVC) membrane on a Si3N4 layer deposited on a Si wafer. We optimized the experimental condition for the fabrication of the PVC membrane, and obtained a PVC membrane with a flat and uniform surface on the scale of several hundreds of micrometer suitable for a substrate for supported lipid bilayers (SLBs). The SLB of 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) was formed on the PVC membrane by the vesicle fusion method. The observation with a conventional epi-fluorescence microscope and a confocal laser scanning microscope gave geometrically uniform images of the SLB on the PVC membrane. The fluidity and the mobile fraction of the SLB was evaluated by the fluorescence recovery after photobleaching method, and compared with that on a thermally oxidized SiO{sub 2}/Si substrate. The SLB on the PVC membrane contained immobile fraction ?30%, but the diffusion in the mobile fraction was two times faster than that in the SLB on SiO{sub 2}/Si, which had little immobile fraction.

  11. Chitosan and polyvinyl alcohol composite films containing nitrofurazone: preparation and evaluation

    PubMed Central

    Kouchak, Maryam; Ameri, Abdolghani; Naseri, Basireh; Kargar Boldaji, Sara

    2014-01-01

    Objective(s): The aim of this study was to insert nitrofurazone in a chitosan membrane to be used as a wound dressing. Materials and Methods: Several blend films using chitosan (Cs) and polyvinyl alcohol (PVA), containing nitrofurazone were prepared by means of casting/solvent evaporating technique. Different characteristics such as mechanical properties, water vapor transmission rate (WVTR), oxygen permeability (OP), swelling ability (SW), differential scanning calorimetric (DSC), drug release profiles and antibacterial activity of the films were investigated. Results: The results showed that nitrofurazone decreased tensile strength, OP and SW of Cs films, while increased WVTR. Addition of PVA at any concentration improved mechanical properties, reduced WVTR, and increased OP and SW of nitrofurazone-loaded Cs films. The latter films showed higher activity against Pseudomonas aeruginosa than drug-free chitosan films. Conclusion: The presence of PVA improves many properties of Cs-nitrofurazone films and makes them more desirable as dressing material for burn wounds. Although nitrofurazone alone is ineffective against P. aeruginosa, it is able to increase antibacterial effect of chitosan in composite films. PMID:24592302

  12. Recycling of waste automotive laminated glass and valorization of polyvinyl butyral through mechanochemical separation.

    PubMed

    Swain, Basudev; Ryang Park, Jae; Yoon Shin, Dong; Park, Kyung-Soo; Hwan Hong, Myung; Gi Lee, Chan

    2015-10-01

    Due to strong binding, optical clarity, adhesion to many surfaces, toughness and flexibility polyvinyl butyral (PVB) resin films are commonly used in the automotive and architectural application as a protective interlayer in the laminated glass. Worldwide million tons of PVB waste generated from end-of-life automotive associated with various environmental issues. Stringent environmental directive, higher land cost eliminates land filling option, needs a study, we have developed a mechanochemical separation process to separate PVB resins from glass and characterized the separated PVB through various techniques, i.e., scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDS), infrared spectroscopy (IR) and nuclear magnetic resonance spectroscopy (NMR). Commercial nonionic surfactants D201 used for the mechanochemical separation purpose. Through parameter optimization following conditions are considered to be the optimum condition; 30vol% D201, stirring speed of 400rpm, 35°C temperature, operation time 1h, and dilute D201 volume to waste automotive laminated glass weight ratio of ?25. The technology developed in our laboratory is sustainable, environmentally friendly, techno-economical feasible process, capable of mass production (recycling). PMID:26318256

  13. Thermochemical reaction mechanism of lead oxide with poly(vinyl chloride) in waste thermal treatment.

    PubMed

    Wang, Si-Jia; Zhang, Hua; Shao, Li-Ming; Liu, Shu-Meng; He, Pin-Jing

    2014-12-01

    Poly(vinyl chloride) (PVC) as a widely used plastic that can promote the volatilization of heavy metals during the thermal treatment of solid waste, thus leading to environmental problems of heavy metal contamination. In this study, thermogravimetric analysis (TGA) coupled with differential scanning calorimeter, TGA coupled with Fourier transform infrared spectroscopy and lab-scale tube furnace experiments were carried out with standard PVC and PbO to explicate the thermochemical reaction mechanism of PVC with semi-volatile lead. The results showed that PVC lost weight from 225 to 230°C under both air and nitrogen with an endothermic peak, and HCl and benzene release were also detected. When PbO was present, HCl that decomposed from PVC instantly reacted with PbO via an exothermal gas-solid reaction. The product was solid-state PbCl2 at <501°C, which was the most volatile lead-containing compound with a low melting point and high vapor pressure. At >501°C, PbCl2 melted, volatilized and transferred into flue gas or condensed into fly ash. Almost all PbCl2 volatilized above 900°C, while PbO just started to volatilize slowly at this temperature. Therefore, the chlorination effect of PVC on lead was apt to lower-temperature and rapid. Without oxygen, Pb2O was generated due to the deoxidizing by carbon, with oxygen, the amount of residual Pb in the bottom ash was significantly decreased. PMID:25150687

  14. Synthesis of magnetic and multiferroic materials from polyvinyl alcohol-based gels

    NASA Astrophysics Data System (ADS)

    Lisnevskaya, I. V.; Bobrova, I. A.; Lupeiko, T. G.

    2016-01-01

    This review article summarizes results on the synthesis of the magnetic materials including modified nickel ferrite (Ni0.9Co0.1Cu0.1Fe1.9O4-?), yttrium iron garnet (Y3Fe5O12), lanthanum-containing manganites (MxLa1-xMnO3 (M=Pb, Ba or Sr; x=0.3-0.35)), and multiferroics (BiFeO3 and BiFe0.5Mn0.5O3) from polyvinyl alcohol-based gels. It is shown that the ammonium nitrate accelerates destruction of organic components of xerogels and thus Ni0.9Co0.1Cu0.1Fe1.9O4-? and BiFeO3 can be prepared at record low temperatures (100 and 250 °C, respectively) which are 200-300 °C lower compared to the process where air is used as an oxidizing agent. As for the synthesis of Y3Fe5O12, MxLa1-xMnO3 and BiFe0.5Mn0.5O3, the presence of NH4NO3 favors formation of foreign phases, which ultimately complicate reaction mechanisms and lead to the higher temperature to synthesize target products. Developed methods provide nanoscale magnetic and multiferroic materials with an average particle size of ?20-50 nm.

  15. Poly(vinyl sulfonate) Facilitates bFGF-Induced Cell Proliferation.

    PubMed

    Nguyen, Thi H; Paluck, Samantha J; McGahran, Andrew J; Maynard, Heather D

    2015-09-14

    Heparin is a highly sulfated polysaccharide and is useful because of its diverse biological functions. However, because of batch-to-batch variability and other factors, there is significant interest in preparing biomimetics of heparin. To identify polymeric heparin mimetics, a cell-based screening assay was developed in cells that express fibroblast growth factor receptors (FGFRs) but not heparan sulfate proteoglycans. Various sulfated and sulfonated polymers were screened, and poly(vinyl sulfonate) (pVS) was identified as the strongest heparin-mimicking polymer in its ability to enhance binding of basic fibroblast growth factor (bFGF) to FGFR. The results were confirmed by an ELISA-based receptor-binding assay. Different molecular weights of pVS polymer were synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization. The polymers were able to facilitate dimerization of FGFRs leading to cell proliferation in FGFR-expressing cells, and no size dependence was observed. The data showed that pVS is comparable to heparin in these assays. In addition, pVS was not cytotoxic to fibroblast cells up to at least 1 mg/mL. Together this data indicates that pVS should be explored further as a replacement for heparin. PMID:26212474

  16. Fabrication and characterization of hybrid nanofibers from poly(vinyl alcohol), milk protein and metal carbonates.

    PubMed

    Mahanta, Narahari; Teow, Yiwei; Valiyaveettil, Suresh

    2012-08-01

    Porous three dimensional nanofibrous membranes were fabricated from poly(vinyl alcohol) (PVA), milk protein and inorganic salts such as calcium carbonate (CaCO3) or magnesium carbonate (MgCO3). Microscopic investigations showed that the fibers have smooth morphology with an average diameter of 300-500 nm and a surface area of 5.29 m2g(-1). Thermal analysis of the composite nanofibers showed a decrease in glass transition temperature as compared to PVA nanofiber. Incorporation of CaCO3 and MgCO3 into the nanofiber matrix was confirmed by energy dispersive spectroscopy and X-ray diffraction analysis. The cytocompatibility of electrospun composite nanofiber sheets was evaluated using human lung fibroblasts (IMR-90). There was an increase in cell attachment and cell density on milk protein incorporated to PVA-CaCO3 and PVA-MgCO3 fibers within a week of cell seeding. The cytocompatibility and increase in cell adhesion property of the hybrid nanofiber may provide significant advantages for such materials in biomedical applications. PMID:22962721

  17. Poly(vinyl alcohol)-heparin biosynthetic microspheres produced by microfluidics and ultraviolet photopolymerisation

    PubMed Central

    Young, Cara; Rozario, Kester; Serra, Christophe; Poole-Warren, Laura; Martens, Penny

    2013-01-01

    Biosynthetic microspheres have the potential to address some of the limitations in cell microencapsulation; however, the generation of biosynthetic hydrogel microspheres has not been investigated or applied to cell encapsulation. Droplet microfluidics has the potential to produce more uniform microspheres under conditions compatible with cell encapsulation. Therefore, the aim of this study was to understand the effect of process parameters on biosynthetic microsphere formation, size, and morphology with a co-flow microfluidic method. Poly(vinyl alcohol) (PVA), a synthetic hydrogel and heparin, a glycosaminoglycan were chosen as the hydrogels for this study. A capillary-based microfluidic droplet generation device was used, and by varying the flow rates of both the polymer and oil phases, the viscosity of the continuous oil phase, and the interfacial surface tension, monodisperse spheres were produced from ?200 to 800??m. The size and morphology were unaffected by the addition of heparin. The modulus of spheres was 397 and 335?kPa for PVA and PVA/heparin, respectively, and this was not different from the bulk gel modulus (312 and 365 for PVA and PVA/heparin, respectively). Mammalian cells encapsulated in the spheres had over 90% viability after 24 h in both PVA and PVA/heparin microspheres. After 28 days, viability was still over 90% for PVA-heparin spheres and was significantly higher than in PVA only spheres. The use of biosynthetic hydrogels with microfluidic and UV polymerisation methods offers an improved approach to long-term cell encapsulation. PMID:24404042

  18. Isolation and molecular characterization of polyvinyl chloride (PVC) plastic degrading fungal isolates.

    PubMed

    Ali, Muhammad Ishtiaq; Ahmed, Safia; Robson, Geoff; Javed, Imran; Ali, Naeem; Atiq, Naima; Hameed, Abdul

    2014-01-01

    The recalcitrant nature of polyvinyl chloride creates serious environmental concerns during manufacturing and waste disposal. The present study was aimed to isolate and screen different soil fungi having potential to biodegrade PVC films. After 10 months of soil burial experiment, it was observed that a number of fungal strains were flourishing on PVC films. On morphological as well as on 18rRNA gene sequence and phylogenetic basis they were identified as Phanerochaete chrysosporium PV1, Lentinus tigrinus PV2, Aspergillus niger PV3, and Aspergillus sydowii PV4. The biodegradation ability of these fungal isolates was further checked in shake flask experiments by taking thin films of PVC (C source) in mineral salt medium. A significant change in color and surface deterioration of PVC films was confirmed through visual observation and Scanning electron microscopy. During shake flask experiments, P. chrysosporium PV1 produced maximum biomass of about 2.57?mg?ml(-1) followed by A. niger PV3. P. chrysosporium PV1 showed significant reduction (178,292?Da(-1)) in Molecular weight of the PVC film than control (200,000?Da(-1)) by gel permeation chromatography. Furthermore more Fourier transform infrared spectroscopy and nuclear magnetic resonance also revealed structural changes in the PVC. It was concluded that isolated fungal strains have significant potential for biodegradation of PVC plastics. PMID:23686796

  19. Composite films of poly(vinyl alcohol)-chitosan-bacterial cellulose for drug controlled release.

    PubMed

    Pavaloiu, Ramona-Daniela; Stoica-Guzun, Anicuta; Stroescu, Marta; Jinga, Sorin Ion; Dobre, Tanase

    2014-07-01

    Mono and multilayer composite films of poly(vinyl alcohol)-chitosan-bacterial cellulose (PVA/chitosan/BC) have been prepared to achieve controlled release of ibuprofen sodium salt (IbuNa) as model drug. The composite films have been characterized by Fourier transformed infrared spectroscopy (FTIR) and X-ray diffraction (XRD). Surface morphology was investigated by scanning electron microscopy (SEM). Equilibrium swelling was measured in water at two different pH values and in vitro release of IbuNa in pH 1.2 and pH 7.4 media was studied. The release experiments revealed that drug release is pH sensitive. The release kinetics of IbuNa could be described by the Fickian model of diffusion with a good agreement. The IbuNa release rate was decreasing for all the films as the BC concentration was increased in the films composition, the decrease being higher for the multilayer films. PMID:24769089

  20. Silver polyvinyl pyrrolidone nanoparticles exhibit a capsular polysaccharide influenced bactericidal effect against Streptococcus pneumoniae

    PubMed Central

    Bibbs, Ronda K.; Harris, Rhonda D.; Peoples, Veolanda A.; Barnett, Cleon; Singh, Shree R.; Dennis, Vida A.; Coats, Mamie T.

    2014-01-01

    Streptococcus pneumoniae remains a leading cause of morbidity and mortality worldwide. The highly adaptive nature of S. pneumoniae exemplifies the need for next generation antimicrobials designed to avoid high level resistance. Metal based nanomaterials fit this criterion. Our study examined the antimicrobial activity of gold nanospheres, silver coated polyvinyl pyrrolidone (AgPVP), and titanium dioxide (TiO2) against various serotypes of S. pneumoniae. Twenty nanometer spherical AgPVP demonstrated the highest level of killing among the tested materials. AgPVP (0.6 mg/mL) was able to kill pneumococcal serotypes 2, 3, 4, and 19F within 4 h of exposure. Detailed analysis of cultures during exposure to AgPVP showed that both the metal ions and the solid nanoparticles participate in the killing of the pneumococcus. The bactericidal effect of AgPVP was lessened in the absence of the pneumococcal capsular polysaccharide. Capsule negative strains, JD908 and RX1, were only susceptible to AgPVP at concentrations at least 33% higher than their respective capsule expressing counterparts. These findings suggest that mechanisms of killing used by nanomaterials are not serotype dependent and that the capsular polysaccharide participates in the inhibition. In the near future these mechanisms will be examined as targets for novel antimicrobials. PMID:25520713