Relevant bibliographies by topics / Ethylen vinyl acetát

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

Academic literature on the topic 'Ethylen vinyl acetát'

Author: Grafiati
Published: 28 June 2021
Last updated: 3 February 2022

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Journal articles on the topic "Ethylen vinyl acetát"

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Jung, Bo Kyoung, Geon Wook Park, Jae-Keun Yu, Hyo Jun Kim, Dong Gun Kim, Minguen Kim, and Kyu Hyun. "Study of Compression Set of Ethylene Vinyl Acetate (EVA) Foams." Polymer Korea 44, no. 3 (May 31, 2020): 264–69. http://dx.doi.org/10.7317/pk.2020.44.3.264.

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Myshak, Volodymyr, Vita Seminog, Volodymyr Grishchenko, and Antonina Barantsova. "Modified composites based on poly(ethylene-vinyl acetate) and crumb rubber." Chemistry & Chemical Technology 11, no. 4 (December 20, 2017): 454–58. http://dx.doi.org/10.23939/chcht11.04.454.

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Fayzullayev, N., F. Buronov, N. Musulmonov, O. Qodirov, and F. Toshboyev. "Effect of the Number of Active Components of the Catalyst on the Yield of the Product During the Synthesis of Vinyl Acetate From Ethylene and Acetic Acid." Bulletin of Science and Practice 7, no. 4 (April 15, 2021): 301–11. http://dx.doi.org/10.33619/2414-2948/65/34.

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The development of active and selective catalysts for the synthesis of vinyl acetate from ethylene and acetic acid, the effect of the amount and ratio of individual components of the catalyst to control the catalytic properties of the introduced components were studied. In vinyl acetate synthesis, the effects of each component were studied to describe the effect of catalyst constituents on its properties, and empirical one-factor mathematical dependencies were obtained. Their generalized mathematical relationships of the activities of the catalysts, defined as the rates of the reactions of the formation of vinyl acetate and CO2, have been proposed. As a result of the research, a mathematical model was proposed to select the most optimal composition of the catalyst. The activity of the catalyst containing 0.4%Pd+4%Cu+7%CH3COOK/HSZ averaged 700 g VA/(l×cat×h) at 93–97% selectivity of ethylene-vinyl acetate formation.
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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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Kim, Seon Yong. "Experimental study on the effects of EVA(Ethylene Vinyl Acetate) for solar cell's long-term life." Journal of the Korea Safety Management and Science 17, no. 4 (December 31, 2015): 397–401. http://dx.doi.org/10.12812/ksms.2015.17.4.397.

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Weng, Tsai-Lung. "Evaluation of cementitious repair mortars modified with polymers." Advances in Mechanical Engineering 9, no. 1 (January 2017): 168781401668858. http://dx.doi.org/10.1177/1687814016688584.

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The aim of this study was to evaluate the effects of added polymers on the properties of repair mortars. Two types of polymers, ethylene vinyl acetate and polyvinyl acetate–vinyl carboxylate, were used as a replacement for 3%, 5%, and 8% of the cement (by weight). All tests were conducted using two water–cement ratios of 0.5 and 0.6. The effectiveness of the repair materials was evaluated according to setting time, drying shrinkage, thermal expansion, compressive strength, and bond strength. Specimens containing polyvinyl acetate–vinyl carboxylate at a water–cement ratio of 0.5 presented the highest compressive and bond strength. Specimens containing ethylene vinyl acetate presented strength characteristics exceeding those of the control at 28 days. The drying shrinkage of polyvinyl acetate–vinyl carboxylate specimens was similar to that of the control. At a water–cement ratio of 0.5, the thermal expansion of polyvinyl acetate–vinyl carboxylate specimens was lower than that of ethylene vinyl acetate specimens; however, at a water–cement ratio of 0.6, the thermal expansion was independent of the type of polymer.
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Ramesh S, Ramesh S., and Punithamoorthy K. Punithamoorthy K. "Synthesis And Characterization Of Ethylene Vinyl Acetate (Eva) / Poly Urethane Acrylate (Pua) Nano Clay Composites." International Journal of Scientific Research 1, no. 4 (June 1, 2012): 8–9. http://dx.doi.org/10.15373/22778179/sep2012/3.

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Xie, Jinchun, Hongfu Yuan, Chunfeng Song, Xiangjun Yan, Hao Yan, and Xiaoyu Li. "Online determination of chemical and physical properties of poly(ethylene vinyl acetate) pellets using a novel method of near-infrared spectroscopy combined with angle transformation." Analytical Methods 11, no. 18 (2019): 2435–42. http://dx.doi.org/10.1039/c9ay00475k.

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SADA, Tomoaki. "Ethylene-Vinyl Acetate Emulsion." Journal of The Adhesion Society of Japan 41, no. 11 (2005): 452–58. http://dx.doi.org/10.11618/adhesion.41.452.

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Go, Sun-Ho, Min-Sang Lee, Chang-Gi Hong, Lee-Ku Kwac, and Hong-Gun Kim. "Correlation between Drop Impact Energy and Residual Compressive Strength According to the Lamination of CFRP with EVA Sheets." Polymers 12, no. 1 (January 16, 2020): 224. http://dx.doi.org/10.3390/polym12010224.

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Carbon-fiber-reinforced plastic is an important building material; however, its application is limited because of its brittleness, leading to vulnerability under shock. Thus, the strength performance of carbon-fiber-reinforced plastics needs to be improved. Here, the drop impact test was conducted to analyze the impact energy and fracture characteristics of carbon-fiber-reinforced plastics and ethylene vinyl acetate sheets. The compression after impact test was performed to assess the residual compressive strength. The thermal energy generated was measured as change in temperature at the time of fracture to investigate the relationship between thermal and mechanical properties. The impact absorption efficiency of 100% was achieved when the carbon-fiber-reinforced plastics specimen was laminated with four or more sheets of ethylene vinyl acetate. The thermal energy generated during impact, the impact load, and the compression after impact test strength was reduced with the increasing number of laminated ethylene vinyl acetate layers. Our results showed that, by carefully selecting the optimal conditions of fabricating the carbon-fiber-reinforced plastic/ethylene vinyl acetate composites, carbon composite materials can be used for impact mitigation.
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Dissertations / Theses on the topic "Ethylen vinyl acetát"

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Langer, Filip. "Vliv okolních podmínek na recyklaci solárních modulů." Master's thesis, Vysoké učení technické v Brně. Fakulta elektrotechniky a komunikačních technologií, 2021. http://www.nusl.cz/ntk/nusl-442429.

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This thesis is focused on experiments, goal of which is to separate protective glass apart from thin layer solar panel. This could lead to less expensive and more efficient recycling. We try to achieve the separation of the glass by thawing ethylene vinyl acetate layer, which serves as insulant and bonding material. Experiments are concluded in high temperature dryer and high temperature vacuum oven on samples of thin layer solar panel, which is for the purposes of experiments cut into same pieces by water jet cutting machine. The initiatory experiments in dryer and oven are to determine value of ethylene vinyl acetate thaw point in tested samples of panel. The thaw point is determined to be 340 °C. When exposed to this temperature, the ethylene vinyl acetate thaws enough for glass to be able to be extracted with minimal physical strength. The process is accompanied by fire destruction of tedlar layer and creation of exhaust gases. Following experiments in vacuum and nitrogen environment are to test their influence on thawing process. Exposing sample to temperature of 340 °C in vacuum led to no new results. Exposing sample to temperature of 340 °C in nitrogen environment prevented fire and achieved same level of thawing of ethylene vinyl acetate while creating less exhaust gases. Even though the fire was prevented, tedlar layer was still destroyed by the high temperature. Furthermore, particles of evaporated ethylene vinyl acetate condensed on surface of module in form of dust. Following experiments studied absorption of panel and influence of accessible solvents on thawing process. It was determined that panel is able to absorb approximately 2 % of acetone, 0,4 % of isopropyl alcohol and 0,11 % of distilled water in its own weight. Experiments with modules soaked in these solvents proved no new results in thawing process. By observing samples of ethylene vinyl acetate taken from module, thawed out of module after experiment in vacuum oven and dust condensed on surface of module after experiment in nitrogen environment, it was proven that the condensed dust is indeed 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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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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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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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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Khan, Shadeed. "Controlled Release of Fluoride from Poly(ethylene-co-vinyl acetate) Films." VCU Scholars Compass, 2009. http://scholarscompass.vcu.edu/etd/1928.

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The development of aesthetically unattractive white spots is a concern for patients undergoing fixed orthodontic treatment. Due to poor oral hygiene during treatment, accumulation of plaque around orthodontic brackets causes bacterial fermentation reactions producing acids that dissolve the mineral enamel. Such dissolution results in white spot formation, an early sign of dental caries. In principal, to inhibit the appearance of these spots during treatment, fluoridated elastomeric o-rings might be employed. Once placed around brackets, these o-rings should release fluoride therapeutically for at least 30 days, after which the orthodontist may replace them. At the present time, such fluoride-releasing o-rings are not available. In this study, model materials for fluoride-releasing elastomeric o-rings were developed. These materials were fluoride-impregnated poly(ethylene-co-vinyl acetate) (PEVA) films. In vitro release studies of these films were conducted, assessing their capacity to deliver fluoride within therapeutic range (1.2 ≤ µg F/ring/day ≤ 51.4) for 30-45 days. Optimal sample and experimental parameters, including (1) fluoride loading in the film (wt% F), (2) overcoat thickness, and (3) temperature that provided therapeutic release, were determined. At 37°C, favorable release was observed for the following: (1) films with overcoat thickness of 0.14 mm and fluoride loadings of 3.9 wt% and 5.7 wt% and (2) films with overcoat thickness of 0.27 mm and fluoride loading of 5.7 wt%. These results are important in providing fundamental guidance for the development of o-rings that combat white spot formation among orthodontic patients.
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Glikman, Jean-François. "Oxydation photo-thermique des copolymeres ethylene-acetate de vinyle, ethylene-acrylate d'ethyle, ethylene-acide acrylique." Clermont-Ferrand 2, 1987. http://www.theses.fr/1987CLF21050.

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Irradiation sous vide et dans l'air. La vitesse d'apparition des produits de photooxydation depend du type de copolymere. Cinetique et mecanisme. Mise en evidence de la labilite croissante de l'atome d'hydrogene tertiaire situe en position alpha des groupes substituants quand on passe de l'acetate a l'ethylate et a l'acide. Influence de charges et de stabilisants
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Bellam, Balaji Anand. "Effect of e-beam sterilization on polypropylene/ethylene propylene diene monomer and ethylene vinyl acetate thermoplastic elastomer." Thesis, University of Nottingham, 2018. http://eprints.nottingham.ac.uk/52484/.

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Thermoplastic elastomer is one of the priority polymeric compound identified for promotion and further development, given the growing demand for a number of commercial industries such as automobile, construction, footwear, healthcare, medical and food packaging sectors. In this study polypropylene (PP)/ethylene propylene diene monomer (EPDM) based thermoplastic elastomers are preferred for improving their properties as it can serve as a good replacement for PP or EPDM material, bridging the gap between thermoset and thermoplastic materials. This study focuses to develop PP/EPDM which can resist changes or improve properties when exposed to E-beam radiation, as E-beam also offers sustainable sterilization at low cost. The PP/EPDM blends with mixing ratios of 80/20, 50/50 and 20/80 were melt blended with the process parameters optimized using Design of experiments (DOE). The effect of E-beam on mechanical properties, thermal stability, crystallization and dynamic mechanical properties over the dose of 0 to 100 kGy were studied. The blends with high EPDM content (20PP/80EPDM) showed improvement in tensile strength up to 36% (at 40kGy and 60kGy) and resistant to impact strength up to 100 kGy, at the expense of elongation at break. On the other hand, the blends with high PP content (80 PP/20 EPDM and 50 PP/50 EPDM) showed detrimental effects on mechanical properties at all radiation dose studied and found to be not compatible for E-beam sterilization. Further, ethylene vinyl acetate (EVA) was incorporated to PP/EPDM blends at 10EVA/40EPDM/50PP, 20EVA/30 EPDM/50PP, 30EVA/20 EPDM/50PP and 40EVA/10 EPDM/50PP ratios. The gel content analysis showed that the efficiency of crosslinking decreased with increase in EVA loading. However, the presence of EVA in ternary blend especially facilitated the induction of sufficient crosslinks leading to improvement in tensile strength (up to 29% at 60 kGy), impact strength (up to 15% at 80 kGy) and retention of stiffness and thermal properties under radiation at the expense of elongation at break. In order to develop antibacterial ternary blends, silver nanoparticles (AgNP) were added by varying the loading from 0.3wt% to 1wt%. The Ag-ternary blends showed enhancement in impact properties (up to 9%) at the expense of decrement in tensile properties due to the agglomeration of AgNP. When, exposed to E-beam radiation, the mechanical and thermal properties exhibited similar trend of increment and decrement across radiation dose similar to the blends without AgNP. While, 1% Ag blend composites showed bacteriostatic effect on Staphylococcus aureuson, no significant reduction of Pseudomonas aeruginosa bacteria was observed. All the blends, before and after sterilization showed no significant toxicity on HaCaT cells investigated using in vitro analysis. Thus, the blends showed an instinct that their application could be extended to manufacturing of healthcare products and food packaging sector, as they are biocompatible and can withstand E-beam sterilization as demanded by the respective application. Among all the blends ternary blends studied (that exhibited biocompatibility even after radiation), 20EVA/30EPDM/50PP without AgNP showed the highest tensile strength of 18.41 MPa and impact strength of 43.64 J/m. Only a slight increase in tensile and impact properties was witnessed upon addition of 20% EVA to PP/EPDM blend in comparison to the binary blend (50PP/50EPDM blend). However, unlike the binary blend (whose properties decreased upon radiation), the ternary blend (20EVA/30EPDM/50PP) showed improvement in tensile strength up to 29% at 60kGy and up to 15% increase in impact strength at 80kGy.
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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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Dommanget, Cédric. "Polymérisation radicalaire contrôlée : le défi de l'éthylène." Thesis, Lyon 1, 2013. http://www.theses.fr/2013LYO10216/document.

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Les travaux présentés dans cette thèse portent sur le contrôle de la polymérisation radicalaire de l'éthylène à basse pression (200 bar) et basse température (70 °C) et sur la synthèse de copolymères à blocs contenant au moins un segment de polyéthylène. Quatre techniques de polymérisation, couramment utilisées en ingénierie macromoléculaire, ont été étudiées : NMP, CMRP, RAFT/MADIX et ESCP. Nos études sur le nitroxyde SG1 (NMP) et le bis(acétylacétonate) de cobalt (CMRP) ont montré que ces composés sont inefficaces pour contrôler la polymérisation de l'éthylène. Un comportement inattendu du bis(acétylacétonate) de cobalt a cependant été mis en évidence. Il semblerait que ces complexes de cobalt favorisent les réactions de couplage entre les radicaux propagateurs. En revanche, la première polymérisation radicalaire contrôlée de l'éthylène a été atteinte grâce à l'utilisation de xanthates (RAFT/MADIX). Les polyéthylènes synthétisés possèdent des masses molaires qui augmentent linéairement avec la conversion et des dispersités faibles. Le caractère pseudo-vivant de la réaction a été démontré par la synthèse de copolymères à blocs poly(acétate de vinyle)-b-polyéthylène. L'utilisation de nitrones (ESCP) a également permis l'introduction d'une fonction réactive au centre des chaînes de polyéthylène et la synthèse de copolymères triblocs de type ABA, où les blocs latéraux A sont en polystyrène ou polyacrylate et le bloc central B est en Polyéthylène
The work presented in this thesis displays the controlled radical polymerization of ethylene at low temperature (70 °C) and low pressure (200 bar) and the synthesis of block copolymers featuring polyethylene segments. Four polymerization techniques, commonly used in macromolecular engineering, were studied: NMP, CMRP, RAFT/MADIX and ESCP. Our investigation of the use of SG1 nitroxide (NMP) and cobalt (II) acetylacetonate (CMRP) as controlling agents demonstrated their inability to control the polymerization of ethylene. Nonetheless, an unexpected reaction with cobalt (II) acetylacetonate was observed. The coupling reaction between propagating radicals appeared to be favored by the presence of this compound. On the other hand, the first controlled polymerization of ethylene was successfully achieved by using xanthate (RAFT/MADIX). A linear increase of molecular weight with conversion and low polydispersities were observed for the produced polyethylenes. The reaction was demonstrated to be a pseudo-living polymerization by the synthesis of block copolymers poly(vinyl acetate)-b-polyethylene. In addition, midchain-functionalized polyethylenes and ABA type block copolymers, with polystyrene or polyacrylate as the A block and polyethylene as the B block, were also prepared using nitrone based polymerization technique (ESCP)
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Books on the topic "Ethylen vinyl acetát"

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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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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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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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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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Elmansy, Nabih Mohamed. Deformation of bituminous highway pavement materials: Effect of mix composition and binder modification by theaddition of ethylene viny acetate on the deformation of bituminous highway pavement mixes... by abotatory dynamic creep testing. Bradford, 1986.

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Book chapters on the topic "Ethylen vinyl acetát"

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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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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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Bashford, David. "Ethylene Vinyl Acetate (EVA)." In Thermoplastics, 164–67. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-009-1531-2_22.

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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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Wohlfarth, Ch. "Solubility parameter of poly(ethylene-co-vinyl acetate)." In Polymer Solutions, 1574. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_925.

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Vansant, E. F. "Ethylene Vinyl Acetate and its Acetoxy-Hydroxide Transformation." In Developments in Plastics Technology —3, 87–117. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4183-0_3.

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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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Giri, Soumen, and Chaoying Wan. "Electronic Applications of Ethylene Vinyl Acetate and Its Composites." In Flexible and Stretchable Electronic Composites, 61–85. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-23663-6_3.

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Frauendorfer, Eric, Muhammad Babar, Timo Melchin, and Wolf-Dieter Hergeth. "Monitoring of Vinyl Acetate–Ethylene Processes: An Industrial Perspective." In Polymer Reaction Engineering of Dispersed Systems, 183–214. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/12_2017_22.

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Wohlfarth, Ch. "Vapor-liquid equilibrium data of poly(vinyl acetate-co-vinyl chloride) in ethyl acetate." In Polymer Solutions, 2311–15. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-88057-8_463.

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Conference papers on the topic "Ethylen vinyl acetát"

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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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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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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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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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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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Azizi, S., C. Oucllet-Plamondon, E. David, and M. F. Frechette. "Electric Response and Thermal Properties of Ethylene Vinyl Acetate/Graphene-based Composite." In 2018 IEEE Conference on Electrical Insulation and Dielectric Phenomena (CEIDP). IEEE, 2018. http://dx.doi.org/10.1109/ceidp.2018.8544801.

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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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Xia, Zhiyong, Daniel W. Cunningham, and John H. Wohlgemuth. "A non-solvent extraction method for measuring gel content of ethylene vinyl acetate." In 2009 34th IEEE Photovoltaic Specialists Conference (PVSC). IEEE, 2009. http://dx.doi.org/10.1109/pvsc.2009.5411712.

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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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Fang, Changqing, Maorong Zhang, and Tiehu Li. "Combined Modification of Asphalt by Waste Polystyrene and Ethylene - Vinyl Acetate Packaging Materials." In 2008 2nd International Conference on Bioinformatics and Biomedical Engineering. IEEE, 2008. http://dx.doi.org/10.1109/icbbe.2008.551.

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