Relevant bibliographies by topics / Copolymers of ethylene vinyl acetate

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Copolymers of ethylene vinyl acetate'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "Copolymers of ethylene vinyl acetate"

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Moura, Isabel, Ana Vera Machado, Regina Nogueira, and V. Bounor-Legare. "Synthesis of Biodegradable Copolymers Based on Ethylene Vinyl Acetate and Polylactic Acid." Materials Science Forum 636-637 (January 2010): 819–24. http://dx.doi.org/10.4028/www.scientific.net/msf.636-637.819.

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In the present study biodegradable copolymers of ethylene vinyl acetate and polylactic acid were synthesized using transesterification reactions, the structure, morphology, mechanical properties and biodegradability of the produced materials were characterized. Ethylene vinyl acetate was modified with polylactic acid in an internal mixer using titanium propoxide as transesterification catalyst. The graft copolymers were characterized by elemental analysis, infrared spectroscopy, rheology, scanning electron microscopy and thermal analysis. Selective extractions for all copolymers were made, and the results indicate that a maximum of 25 % of EVA-g-PLA copolymer was synthesized by this method. Biodegradation tests were carried out using the standard ISO 14851 (1999), which specifies a method for determining the biochemical oxygen demand in a closed respirometer. This procedure allowed to synthesize biodegradable copolymers with mechanical properties similar to conventional polymers.
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Aliev, A. D., M. A. Vokal’, A. E. Chalykh, and V. K. Gerasimov. "Phase diagrams of ethylene-vinyl acetate copolymers." Polymer Science Series A 48, no. 12 (December 2006): 1281–86. http://dx.doi.org/10.1134/s0965545x06120091.

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Arsac, A., C. Carrot, and J. Guillet. "Rheological characterization of ethylene vinyl acetate copolymers." Journal of Applied Polymer Science 74, no. 11 (December 9, 1999): 2625–30. http://dx.doi.org/10.1002/(sici)1097-4628(19991209)74:11<2625::aid-app9>3.0.co;2-g.

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McGrattan, Brian J. "Examining the Decomposition of Ethylene-Vinyl Acetate Copolymers Using TG/GC/IR." Applied Spectroscopy 48, no. 12 (December 1994): 1472–76. http://dx.doi.org/10.1366/0003702944027750.

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With a combination of information from TG/IR and GC/IR measurements of the trapped gases, characterization of complex polymer decompositions can be made. In this paper, the thermally induced breakdown of ethylene-vinyl acetate (EVA) copolymers was studied. Results show that EVA undergoes a two-step decomposition: an acetate pyrolysis of the copolymer leaving a polyunsaturated linear hydrocarbon, followed by the breakdown of the hydrocarbon backbone to produce a large number of straight-chain hydrocarbon products.
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Bui, Nhi Dinh, Ngo Dinh Vu, Thao Thi Minh, Huong Thi Thanh Dam, Regina Romanovna Spiridonova, and Semenovich Alexandr Sirotkin. "Effect of Acetate Group Content in Ethylene-Vinyl Acetate Copolymer on Properties of Composite Based on Low Density Polyethylene and Polyamide-6." International Journal of Polymer Science 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/3149815.

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The effect of the content of vinyl acetate groups in ethylene-vinyl acetate copolymer on the properties of polymer composite based on low density polyethylene and polyamide-6 was studied. Ethylene-vinyl acetate copolymer containing less vinyl acetate groups (10–14 wt.%) has a positive compatibility effect on polymer composite than ethylene-vinyl acetate copolymer containing 21–30 wt.% vinyl acetate groups. The polymer composites of LDPE, PA-6, and EVA containing 10–14 wt.% vinyl acetate groups possess the ability of biodegradation. The physical-mechanical properties of sample and molecular mass reduce after 28 days of incubation.
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Marie, Emmanuelle, Yves Chevalier, Nathalie Issartel, Franck Eydoux, Laurent Germanaud, and Philippe Flores. "The Controlled Solvolysis of Ethylene−Vinyl Acetate Copolymers." Macromolecules 34, no. 17 (August 2001): 5838–47. http://dx.doi.org/10.1021/ma0102666.

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Henderson, A. M. "Ethylene-vinyl acetate (EVA) copolymers: a general review." IEEE Electrical Insulation Magazine 9, no. 1 (January 1993): 30–38. http://dx.doi.org/10.1109/57.249923.

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Chalykh, A. E., V. Yu Stepanenko, A. A. Shcherbina, and E. G. Balashova. "Adhesive properties of ethylene and vinyl acetate copolymers." Polymer Science. Series D 2, no. 1 (January 2009): 8–15. http://dx.doi.org/10.1134/s199542120901002x.

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Panchev, I., R. Velichkova, A. Dworak, and R. C. Schulz. "Branched polymers starting from ethylene-vinyl acetate copolymers." Reactive and Functional Polymers 27, no. 1 (October 1995): 53–59. http://dx.doi.org/10.1016/1381-5148(95)00034-d.

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Chowdhury, F., J. A. Haigh, L. Mandelkern, and Rufina G. Alamo. "The supermolecular structure of ethylene-vinyl acetate copolymers." Polymer Bulletin 41, no. 4 (October 14, 1998): 463–70. http://dx.doi.org/10.1007/s002890050388.

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Dissertations / Theses on the topic "Copolymers of ethylene vinyl acetate"

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Auden, Noel Geraint. "Ethylene-vinyl acetate copolymers." Thesis, Lancaster University, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.239046.

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Hatzinikolaou, Theodosios A. "Adhesion of ethylene vinyl acetate copolymers to metals." Thesis, University of Bath, 1985. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.355114.

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The 180° peel strength of four ethylene vinyl acetate copolymers with varying V.A. content was measured (Pol A: 28%, Pol B: 18%, Pol C: 12% and Pol D: 9.5% by weight). The polymers were applied as hot-melts with or without an inextensible fabric support on: (a) mild steel etched in hydrochloric acid; (b) chemically polished copper and; (c) oxidised copper with a fibrous topography. The peel loads for a given polymer decreased from oxidised copper to etched steel to polished copper. For a given substrate the peel loads generally decreased from polymer A to polymer D with a peak for polymer C. This trend was correlated to similar trends obtained in mechanical tests like the tearing energy, strain energy density and tensile strength to failure. The fractured parts of the bond were examined with a scanning electron microscope. There was microscopic evidence of an analogy between the peel load and the observed extent of polymer deformation in the fractured surfaces where the ductilty of the particular polymer and the topography of the substrate were clearly depicted. Contact angle measurement showed a cohesive type of failure in all cases. X-ray photo-electron spectroscopy and multiple internal reflection infra-red spectroscopy provided evidence of polymer oxidation by the substrate, mostly significant in the case of etched steel. The energy balance approach was employed in order to analyse the peel test results further. The polymers response to the imposed mechanical deformations during peeling was shown to control the measured peel load. For the unbacked samples the major energy loss mechanism is the stretching of the freed strip. The much higher peel loads of the backed samples were attributed to energy losses around the peel front. Finally, plastic bending of the polymer was found to account for a relatively smaller part of the total input energy for both backed and unbacked samples.
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Clough, Norman E. "Thermodynamics of ethylene-vinyl acetate copolymer blends." Thesis, Durham University, 1994. http://etheses.dur.ac.uk/5489/.

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The purpose of this study was to characterise the miscibility of several poly(ethylene-co-vinyl acetate), EVA, based polymer blends. EVA has many industrial applications and is often present as one of several polymeric components. Consequently, there is considerable interest in the thermodynamics of these blend systems. The thermodynamics of these blends was studied using several techniques: differential scanning calorimetry; phase contrast optical microscopy; small angle neutron scattering and wide angle X-ray scattering. Characterisation was also to include assessing the relative enthalpic and entropic thermodynamic contributions to the Rory-Huggins interaction parameter (%) of these blends. To determine the enthalpic interaction parameter, a "mixing calorimeter" was designed and constructed to measure accurately the "heat of mixing" values on blending these polymers. Free energy interaction parameters were determined from melting point depression and small angle neutron scattering measurements. In all the blends studied, the heat of mixing was endothermic and consequently, the enthalpic interaction parameters were positive i.e. unfavourable to miscibility. Miscibility in these blends can therefore only be achieved by a dominant entropic contribution, favourable to miscibility. Using phase contrast optical microscopy, both miscible and immiscible phase behaviour was observed in this series of blends. This shows good agreement with predictions of miscibility from heat of mixing, melting point and small angle neutron scattering measurements, based on the classical Flory-Huggins lattice theory. Wide angle X-ray scattering and differential scanning calorimetry results have associated miscible blends with crystallisation effects between the blend components. Small angle neutron scattering has been used to determine the concentration and temperature dependence of interaction parameters in a miscible blend. From these values the upper critical solution temperature (UCST) of the blend was predicted. The enthalpic contributions to these interaction parameters show good agreement with experimental values determined from heat of mixing measurements. It was concluded that the classical Flory-Huggins lattice theory (despite its many well documented Limitations) appears to be particularly suited to the thermodynamic characterisation of miscibility in these polymer blends.
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Okpe, Owoicho. "Alumina trihydrate as a fire retardant for ethylene vinyl acetate copolymer." Thesis, University of Manchester, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.339740.

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Khunniteekool, Chonlada. "Structure/property relationships of cross-linked polyethylene and ethylene vinyl acetate copolymer foams." Thesis, University of Manchester, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390453.

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Nuamthanom, Anuttra. "Multidimensional NMR studies of poly(ethylene-co-1-octene) copolymers and poly(ethylene-co-vinyl acetate-co-carbon monoxide) terpolymers." University of Akron / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=akron1183614323.

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Schofield, Wayne Christopher Edward. "Factors affecting the performance of magnesium hydroxide flame retardant fillers in an ethylene vinyl acetate copolymer." Thesis, Manchester Metropolitan University, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297579.

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Bergerbit, Cédric. "RAFT polymerization of ethylene for the synthesis of polar-apolar olefin block copolymers." Thesis, Lyon, 2019. https://n2t.net/ark:/47881/m6s181w9.

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La synthèse de copolymères à blocs, comprenant un bloc semi-cristallin de polyéthylène (PE) apolaire et un bloc polaire (poly(acétate de vinyle) (PAcV), poly(méthacrylate de méthyle) (PMAM), poly(oxide d’éthylène) (POE)) a été étudiée par polymérisation RAFT. L’étude préliminaire de l’homopolymérisation de l’éthylène en conditions relativement douces (T = 70 – 80 °C, P = 200 bar) a révélé que l’utilisation d’agents de transfert de chaîne (ATC) de type xanthates aromatiques conduit à une perte de fonctionnalité des extrémités de chaînes au cours de la polymérisation, conséquence directe de réactions de terminaison se produisant sur le radical intermédiaire. L’utilisation de dithiocarbamates aromatiques a permis de s’affranchir de ce mécanisme parasite et pour la première fois des chaînes de PE présentant une fonctionnalité de bout de chaîne proche de 100%. Des ATCs macromoléculaires polaires, obtenus avec les agents de transfert de chaînes identifiés au cours de l’étude préliminaire, ont ensuite été utilisés pour la synthèse de copolymères à blocs dans le carbonate de diméthyle (DMC), un solvant organique peu transférant. Le rôle clé de la thermodynamique du milieu de polymérisation (mélange DMC/éthylène supercritique à 200 bar) a alors été mis en évidence. En effet, les macro-ATCs sont insolubles dans un tel milieu, ce qui a conduit à la formation d’un mélange d’homopolymères. La diminution de la pression de polymérisation (P < 100 bar) a toutefois permis d’éviter ce phénomène et les copolymères PVAc-b-PE, PMMA-b-PE et PEO-b-PE attendus ont été obtenus. Des propriétés d’auto-assemblage ont été mises en évidence et des morphologies de type fibre ont été obtenues pour les copolymères PMMA-b-PE et PEO-b-PE synthétisés dans le DMC, permettant d’envisager un mécanisme de type auto-assemblage induit par la polymérisation (PISA). Le passage en milieu aqueux en utilisant le macro-ATC hydrosoluble PEO a permis l’observation de morphologies de type sphériques, vésicules ou encore ellipsoïdes selon le rapport molaire macro-ATC/amorceur utilisé
The synthesis of polar-apolar olefin block copolymers, combining a semi-crystalline polyethylene (PE) block and a polar block (poly(vinyl acetate) (PVAc), poly(methyl methacrylate) (PMMA), poly(ethylene oxide) (PEO)) was investigated by RAFT polymerization. A preliminary study on ethylene homopolymerization revealed parasite cross-termination reactions happening at the intermediate radical, resulting in the loss of chain-end fidelity when using aromatic xanthates as chain transfer agents (CTA) under relative mild conditions (T = 70 – 80 °C, P = 200 bar). The extent of cross-termination was greatly reduced with aromatic dithiocarbamates, and for the first time, PE chains with a high livingness were obtained. These first results were used to equip polar macromolecular CTAs (PVAc, PMMA, PEO), with selected aromatic xanthates and dithiocarbamates, that were further used for block copolymerization with ethylene in a low-transferring organic solvent (dimethyl carbonate, DMC). A critical influence of the ethylene pressure was evidenced as block polymerization at 200 bar could not be achieved due to solubility issues in the resulting supercritical DMC/ethylene mixture. This was circumvented by performing the block copolymerization below the supercritical point of the mixture (P < 100 bar) and well-defined PVAc-b-PE, PMMA-b-PE and PEO-b-PE copolymers were eventually obtained. The block copolymers were found to feature self-assembly properties and worm-like morphologies were observed for PMMA-b-PE and PEO-b-PE synthesized in DMC, hinting at a plausible polymerization-induced self-assembly (PISA) mechanism. The successful switch from DMC to water for the synthesis of PEO-b-PE copolymers enabled the observation of various particle morphologies: spheres, vesicles and ellipsoidal particles, depending on the initial macro-CTA:initiator molar ratio
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Rodriguez-Vazquez, Miguel. "Thermal and photo degradation and stabilisation of an ethylene vinyl acetate copolymer in the presence of air." Thesis, Manchester Metropolitan University, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289615.

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Alencar, Ana Ellen Valentim de. "Estudo das propriedades do cimento asfÃltico de petrÃleo modificado por copolÃmero de etileno e acetato de vinila(eva)." Universidade Federal do CearÃ, 2005. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=1439.

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CoordenaÃÃo de AperfeiÃoamento de Pessoal de NÃvel Superior
Cimento AsfÃltico de PetrÃleo (CAP), caracterizado como CAP 50/60, oriundo do Campo Fazenda Alegre, no estado do EspÃrito Santo, foi modificado por adiÃÃo de CopolÃmero de Etileno e Acetato de Vinila (EVA). Na modificaÃÃo foram incorporadas amostras do copolÃmero EVA puro e proveniente do resÃduo da indÃstria de calÃados (EVAR). Os CAPS, polÃmeros e CAPS modificados, foram inicialmente caracterizados por espectroscopia no infravermelho (FTIR) e ressonÃncia magnÃtica nuclear (RMN). AnÃlise tÃrmica, como a termogravimetria (TG) e caloria exploratÃria diferencial (DSC), foi utilizada para o estudo da decomposiÃÃo tÃrmica, bem como para avaliar a estabilidade termoxidativa das amostras. Testes empÃricos como penetraÃÃo, ponto de amolecimento, susceptibilidade tÃrmica e retorno elÃstico, alÃm de viscosidade, tambÃm foram realizados para caracterizaÃÃo dos materiais. Os resultados indicaram que CAPS modificados apresentaram maior estabilidade em atmosfera oxidativa do que em atmosfera inerte. A anÃlise das curvas DSC revelou que os CAPS modificados mostraram-se mais resistentes à trincas tÃrmicas, quando submetidos a temperaturas mais baixas, que o CAP convencional. Os CAPS modificados foram mais resistentes à decomposiÃÃo oxidativa, quando foram submetidos ao envelhecimento simulado. A viscosidade do ligante modificado por adiÃÃo do polÃmero foi aumentada em relaÃÃo ao ligante puro. Diferentemente do CAP convencional, o CAP modificado por EVAR apresentou comportamento nÃo Newtoniano. Os ensaios empÃricos, relativos à penetraÃÃo, ponto de amolecimento, susceptibilidade tÃrmica e retorno elÃstico, mostraram que os CAPS modificados com EVAR, tiveram uma melhoria nas suas propriedades fÃsicas, em relaÃÃo aos CAPS nÃo modificados.
The Petroleum Asphaltic Cement characterized as CAP 50/60, produced at the state of EspÃrito Santo (Fazenda Alegre), was modified by addition of copolymers of ethylene vinyl acetate (EVA) and EVA from the footwearâs industry residue (EVAR). The original and modified CAPS were characterized by infrared spectroscopy (FTIR) and nuclear magnetic resonance (RMN). Thermal analysis,as thermogravimetry (TG) and differential scanning calorimetry (DSC), was used to evaluate the thermal stability of the samples. The characterization was also performed with empirical tests such as penetration, softening point, elastic recovery and viscosity. The main results indicated that polymer modified CAPS presented larger thermal stability in oxidative atmosphere than in inert atmosphere. The analysis of DSC curves revealed that modified CAPS, when submitted to lower temperatures, were more resistant to the thermal cracks than conventional CAP. Also modified CAPS showed to be more resistant to the thermal oxidative decomposition, when submitted to a simulated aging process. The viscosity of the polymer modified binder was increased in relation to the original binder. Polymer modified CAP EVAR presented non-Newtonian behavior, whereas Newtonian behavior was observed for unmodified CAP. It was observed that modifying the asphalt binder with a copolymer EVAR leads to an improvement in the physical properties in relation to the penetration, softening point, thermal susceptibility and elastic recovery
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Books on the topic "Copolymers of ethylene vinyl acetate"

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Clarke, S. D. The characterization of ethylene-vinyl acetate copolymers. Wolverhampton: University ofWolverhampton, 1993.

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Khunniteekool, Chonlada. Structure/property relationships of cross-linked polyethylene and ethylene vinyl acetate copolymer foams. Manchester: UMIST, 1995.

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Institute, Canadian Conservation, ed. Towards a better emulsion adhesive for conservation: A preliminary report on the effect of modifiers on the stability of a vinyl acetate/ethylene (VAE) copolymer emulsion adhesive. Ottawa: Canadian Conservation Institute, 2000.

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Parker, Philip M. The World Market for Ethylene-Vinyl Acetate Copolymers in Primary Forms: A 2007 Global Trade Perspective. ICON Group International, Inc., 2006.

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The World Market for Ethylene-Vinyl Acetate Copolymers in Primary Forms: A 2004 Global Trade Perspective. Icon Group International, Inc., 2005.

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Parker, Philip M. The 2007 Import and Export Market for Ethylene-Vinyl Acetate Copolymers in Primary Forms in China. ICON Group International, Inc., 2006.

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Schofield, Wayne Christopher Edward. Factors affecting the performance of magnesium hydroxide flame retardant fillers in an ethylene vinyl acetate copolymer. 1999.

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Rodriguez-Vazquez, Miguel. Thermal and photo degradation and stabilisation of an ethylene vinyl acetate copolymer in the presence of air. 2003.

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The World Market for Vinyl Chloride-Vinyl Acetate Copolymers in Primary Forms: A 2004 Global Trade Perspective. Icon Group International, Inc., 2005.

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Parker, Philip M. The World Market for Vinyl Chloride-Vinyl Acetate Copolymers in Primary Forms: A 2007 Global Trade Perspective. ICON Group International, Inc., 2006.

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Book chapters on the topic "Copolymers of ethylene vinyl acetate"

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Whelan, Tony, and John Goff. "Ethylene Vinyl Acetate Copolymers." In Injection Molding of Thermoplastic Materials - 2, 49–59. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4757-5502-2_3.

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Gooch, Jan W. "Ethylene–Vinyl Acetate Copolymer." In Encyclopedic Dictionary of Polymers, 281. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_4601.

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MOSKALA, E. J., J. P. RUNT, and M. M. COLEMAN. "Poly(vinylphenol) Blends with Poly(vinyl Acetate) and Ethylene-Vinyl Acetate Copolymers." In Advances in Chemistry, 77–85. Washington, DC: American Chemical Society, 1985. http://dx.doi.org/10.1021/ba-1986-0211.ch005.

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Deanin, Rudolph D., Sujal S. Rawal, Nikhil A. Shah, and Jan-Chan Huang. "Polyblends of Polyvinyl Chloride with Ethylene-Vinyl Acetate Copolymers." In Advances in Chemistry, 403–13. Washington, DC: American Chemical Society, 1989. http://dx.doi.org/10.1021/ba-1989-0222.ch020.

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Robeson, Lloyd M., David Dubowik, and Robert A. Berner. "Water-Based Hybrids of Vinyl Acetate-Ethylene Copolymers and Cross-Linkable Epoxy." In ACS Symposium Series, 338–56. Washington, DC: American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2002-0801.ch023.

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Demarteau, Jérémy, Anthony Kermagoret, Christine Jérôme, Christophe Detrembleur, and Antoine Debuigne. "Controlled Synthesis of Ethylene-Vinyl Acetate Based Copolymers by Organometallic Mediated Radical Polymerization." In ACS Symposium Series, 47–61. Washington, DC: American Chemical Society, 2015. http://dx.doi.org/10.1021/bk-2015-1188.ch004.

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McGrattan, Brian J. "Decomposition of Ethylene—Vinyl Acetate Copolymers Examined by Combined Thermogravimetry, Gas Chromatography, and Infrared Spectroscopy." In ACS Symposium Series, 103–15. Washington, DC: American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0581.ch008.

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Coiado, Renata D. S., Gisele D. Lazo, Rene R. Oliveira, Rita C. L. B. Rodrigues, and Esperidiana A. B. Moura. "Polymer Blend Based on Recycled Polyethylene and Ethylene Vinyl Acetate Copolymers Reinforced with Natural Fibers from Agricultural Wastes." In Characterization of Minerals, Metals, and Materials 2017, 689–97. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-51382-9_76.

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Zaji, Mahdieh, and Masoud Frounchi. "Mechanical Properties of Poly(Lactic Acid)/Ethylene-Vinyl Acetate Copolymer/Nanoclay Composites as Biodegradable Packaging Films." In Eco-friendly and Smart Polymer Systems, 507–10. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-45085-4_123.

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Dollinger, Harli M., and Samuel P. Sawan. "Bicontinuous Controlled-Release Matrices Composed of Poly(D,L-lactic acid) Blended with Ethylene—Vinyl Acetate Copolymer." In ACS Symposium Series, 181–93. Washington, DC: American Chemical Society, 1991. http://dx.doi.org/10.1021/bk-1991-0469.ch017.

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Conference papers on the topic "Copolymers of ethylene vinyl acetate"

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Izutsu, Tomoyuki, Daisuke Odaka, Marina Komatsu, Yoshimichi Ohki, Maya Mizuno, Yoshiaki Nakamura, and Naofumi Chiwata. "Terahertz and far-infrared spectroscopic estimation of vinyl acetate content in ethylene-vinyl acetate copolymer." In 2015 IEEE Conference on Electrical Insulation and Dielectric Phenomena - (CEIDP). IEEE, 2015. http://dx.doi.org/10.1109/ceidp.2015.7351988.

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Richaud, Emmanuel, Amar Bellili, and Yannick Goutille. "Diffusion of mineral oils in ethylene-vinyl acetate copolymer." In 6TH INTERNATIONAL CONFERENCE ON TIMES OF POLYMERS (TOP) AND COMPOSITES. AIP, 2012. http://dx.doi.org/10.1063/1.4738392.

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Wu, Tianzhun, Lifang Yuan, Tao Peng, and Zhiwei Wang. "Ethylene Vinyl Acetate Copolymer-Based High-Adhesion, Low-Cost and Superlyophobic Dry Adhesives." In The 7th International Multidisciplinary Conference on Optofluidics 2017. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/optofluidics2017-04234.

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Jin Li, Hang Xu, Boxue Du, Mingli Fu, and Shuai Hou. "Space charge accumulation characteristics in ethylene-vinyl acetate copolymer filled with ZnO nanoparticles." In 2016 IEEE International Conference on Dielectrics (ICD). IEEE, 2016. http://dx.doi.org/10.1109/icd.2016.7547574.

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Yuan, Lifang, Tianzhun Wu, and Zhiwei Wang. "High-performance polymer dry adhesives based on ethylene vinyl acetate copolymer and high-adhesion mechanism*." In 2018 40th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2018. http://dx.doi.org/10.1109/embc.2018.8512727.

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Dong, W. Z., Z. D. Han, and B. Z. Han. "Boron nitride filled immiscible blends of polyethylene and ethylene-vinyl acetate copolymer: Morphology and dielectric properties." In 2012 IEEE 10th International Conference on the Properties and Applications of Dielectric Materials (ICPADM). IEEE, 2012. http://dx.doi.org/10.1109/icpadm.2012.6319033.

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Zhang, Yong, Zhi Wang, Chenhui Li, Zhe Chen, and Pengfei Fang. "Correlation study between the rheological property and the free volume for ethylene vinyl acetate copolymer under melt extrusion." In 2nd Japan–China Joint Workshop on Positron Science (JWPS2013). Japan Society of Applied Physics, 2014. http://dx.doi.org/10.7567/jjapcp.2.011201.

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Kempe, Michael D., Gary J. Jorgensen, Kent M. Terwilliger, Tom J. McMahon, Cheryl E. Kennedy, and Theodore T. Borek. "Ethylene-Vinyl Acetate Potential Problems for Photovoltaic Packaging." In Conference Record of the 2006 IEEE 4th World Conference on Photovoltaic Energy Conversion. IEEE, 2006. http://dx.doi.org/10.1109/wcpec.2006.279933.

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Agoudjil, B., L. Ibos, Y. Candau, and J. C. Majeste. "Dielectric and thermophysical properties of Ethylene Vinyl Acetate/BaTiO3 composites." In 2007 IEEE International Conference on Solid Dielectrics. IEEE, 2007. http://dx.doi.org/10.1109/icsd.2007.4290833.

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Shady, Sally F., and Stephen McCarthy. "Effects of Vinyl Acetate Content and Extrusion Temperatures on Ethylene Vinyl Acetate (EVA) Tetracycline HCL Fibers Used for Periodontal Applications." In ASME 2016 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/imece2016-66216.

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Abstract:
Periodontal disease is a prevalent disease that effects all types of ages. Mild cases of periodontal disease include infection and gingivitis. Severe cases of periodontal disease include loss of teeth, and the increased likelihood of systemic diseases such as: cancer, osteoporosis and pneumonia. Current treatments of periodontal disease include systemic approaches such as oral tablets of antibiotics or localized treatments such as the periodontal chip. Oral antibiotics require high dosages to effectively treat the infection therefore causing unwanted side effects. Other treatments include surgery, scaling and rooting. These methods have disadvantages as they are more invasive and require long term maintenance. The aim of this study was to develop a periodontal fiber containing Tetracycline HCl and ethylene vinyl acetate (EVA) that can be implanted in the periodontal pocket and demonstrate a drug release for up to 10 days. To develop this drug-embedded fiber, ethylene vinyl acetate and tetracycline HCL were combined and subsequently formed into a fiber. First, both materials were melted and mixed for several minutes in a Brabender mixer. The resulting material was then pelletized and the fiber was synthesized using the hot melt extrusion process. To produce the most optimal fiber, various vinyl acetate contents were mixed and extruded at high and low processing temperatures. The fiber uniformity, tensile strength, and drug release was tested on three groups: 40% vinyl acetate with low processing temperatures, 40% vinyl acetate with high processing temperatures and 7% vinyl acetate with low processing temperatures. To test the uniformity of the fiber, an inline IR reader was used to monitor the outer diameter of the fiber. Since a 0.5mm would be easily implanted into the periodontal pocket, this was the desired fiber dimension. The Instron was used to analyze the tensile strength of each group to ensure that the fiber was durable enough to withstand the harsh environment of the oral cavity. For the drug release testing the fibers were placed into H2O and incubated to 37°C. Samples from the release media were taken at various time intervals for a total of 10 days. The samples were tested on the UV spectrophotometer for peak absorbances at 360nm. The IR reader testing showed that the Elvax 40W (40% vinyl acetate content) material was easier to extrude than the Innospec (7% vinyl acetate content). The tensile strength tests of the fibers were approximately 0.025 ± 0.05 MPa. In-vitro drug release studies indicated that the low processing temperatures fibers released approximately three times the amount of tetracycline HCl than the high processing temperature group. This indicated that the fibers with low processing temperatures had the most favorable drug release profiles for bacterial inhibition. The overall feasibility for the periodontal fiber application was demonstrated in the 40% vinyl acetate group at lower processing temperatures and has shown the potential for multiple antimicrobial applications.
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