Relevant bibliographies by topics / Vinyl acetate

Academic literature on the topic 'Vinyl acetate'

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Published: 4 June 2021
Last updated: 5 March 2023

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Journal articles on the topic "Vinyl acetate"

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Bolt, Hermann. "Vinyl acetate." Toxicology 226, no. 1 (September 2006): 19. http://dx.doi.org/10.1016/j.tox.2006.05.030.

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Luttrell, William E. "Vinyl acetate." Journal of Chemical Health and Safety 20, no. 6 (November 2013): 35–37. http://dx.doi.org/10.1016/j.jchas.2013.10.007.

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Markley, Thomas J., Robert K. Pinschmidt, and John W. Vanderhoff. "Grafting reactions of vinyl acetate onto poly[(vinyl alcohol)-co-(vinyl acetate)]." Journal of Polymer Science Part A: Polymer Chemistry 34, no. 13 (September 30, 1996): 2581–94. http://dx.doi.org/10.1002/(sici)1099-0518(19960930)34:13<2581::aid-pola4>3.0.co;2-v.

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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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Resa, J. M., C. González, B. Moradillo, and J. Lanz. "(Vapour + liquid) equilibria for (methanol + butyl acetate), (vinyl acetate + butyl acetate), (methanol + isobutyl acetate), and (vinyl acetate + isobutyl acetate)." Journal of Chemical Thermodynamics 30, no. 10 (October 1998): 1207–19. http://dx.doi.org/10.1006/jcht.1998.0385.

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Nurlela, Nurlela, and Risnawati Risnawati. "PENGARUH RESIN TERHADAP PERUBAHAN WARNA PADA CAT TEMBOK." JURNAL SAINS NATURAL 5, no. 2 (December 16, 2019): 132. http://dx.doi.org/10.31938/jsn.v5i2.264.

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The Influence of Resin against the Change of Color on the Wall PaintThe quality of the paint is determined by the resin used. Synthetic resins for polymer paints are made by combining several monomers to achieve various characteristics. The incorporation of some monomers such as polyvinyl acetate resin, acrylic vinyl resin and acrylic styrene resin which act as a binder can affect the quality of the paint especially the color change. The purpose of this study is to find the color changes that occur on the wall paint by using Poly Styrene Acrylic , Poly Vinyl Acetate and Poly Vinyl Acrylic. From the results of the measurement of color difference, significant color change occurs in the Poly Vinyl Acetate (PVAc) + Poly Vinyl Acrylic (PVA) and Poly Styrene Acrylic (PSA). The results of the quality test of the three resins based on pH test, scrub test and viscosity test, PSA has better quality compared to PVA + PVAc and PVA resin. From the color difference measurement test, some things need to be considered, are temperature, film thickness, substrate color/background color and measurement conditions (measured in wet sample/in plate/dry surface) and test on resin added additive according to the type of each resin.Keywords: Paint, Resin, Color Changes, Poly Vinyl Acetate, Poly Styrene.ABSTRAK Kualitas dari cat sangat ditentukan oleh resin yang digunakan. Resin sintetis untuk cat berupa polimer yang dibuat dengan menggabung beberapa monomer untuk mencapai berbagai karakteristik. Penggabungan dari beberapa monomer seperti resin poli vinil asetat, resin vinil akrilik dan resin stirena akrilik yang berfungsi sebagai pengikat mampu mempengaruhi kualitas cat terutama dari perubahan warna. Tujuan dari penelitian ini adalah untuk mengetahui perubahan warna yang terjadi pada cat tembok dengan menggunakan Poli Stirena Akrilik, Poli Vinil asetat dan Poli Vinil Akrilik. Dari hasil pengukuran perbedaan warna, perubahan warna cukup signifikan terjadi pada resin Poli vinil Asetat (PVAc) + Poli Vinil Akrilik (PVA) dan resin Poli Stirena Akrilik (PSA). Hasil uji Kualitas cat dari ketiga resin berdasarkan uji pH, uji scrub dan uji viscositas, PSA memiliki kualitas yang lebih baik dibandingkan dengan resin PVA+PVAc dan PVA. Dari pengujian pengukuran perbedaan warna, beberapa hal yang perlu di perhatikan, yaitu suhu, film thickness, warna substrat/background color dan kondisi pengukuran (diukur dalam keadaan wet sample/dalam bentuk plate/dry surface) dan pengujian terhadap resin yang ditambahkan zat aditif yang sesuai dengan tipe masing-masing resin tersebut.Kata Kunci: Cat, Resin, Perubahan Warna, Poli Vinil, Poli Stirena.
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Wisniak, Jaime, and Abraham Tamir. "The systems vinyl acetate-toluene and vinyl acetate-propyl bromide-toluene." Journal of Chemical & Engineering Data 34, no. 3 (July 1989): 301–5. http://dx.doi.org/10.1021/je00057a013.

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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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Jung, Hye Min, Eun Mi Lee, Byung Chul Ji, Sung Ok Sohn, Han Do Ghim, Hyunju Cho, Young A. Han, Jin Hyun Choi, Jae Deuk Yun, and Jeong Hyun Yeum. "Preparation of poly(vinyl acetate)/clay and poly(vinyl acetate)/poly(vinyl alcohol)/clay microspheres." Fibers and Polymers 7, no. 3 (September 2006): 229–34. http://dx.doi.org/10.1007/bf02875677.

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Rees, Gwilym J. "Synthesis of vinyl phenyl acetate and an evaluation of vinyl chloride/vinyl phenyl acetate copolymers." Journal of Applied Polymer Science 43, no. 2 (July 20, 1991): 341–45. http://dx.doi.org/10.1002/app.1991.070430212.

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Dissertations / Theses on the topic "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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Croot, Robert Arthur. "The characterisation and adsorption of vinyl alcohol vinyl acetate copolymers." Thesis, University of Bristol, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303767.

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De, Bruyn Hank. "The Emulsion Polymerization of Vinyl Acetate." Thesis, The University of Sydney, 1999. http://hdl.handle.net/2123/381.

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Abstract This work investigates the kinetics of the emulsion polymerization of vinyl acetate. Several aspects of this system have been clarified, including the induced decomposition of persulfate, retardation by oxygen and entry by, and analysis of, the aqueous phase oligomeric radicals. It has been shown that the retardation period observed in the emulsion polymerization of VAc can be explained by the effect of traces of oxygen (< 10-6 M) on the entry efficiency of the initiator-derived aqueous-phase oligomeric radicals. Comparison of rates of polymerization in V and persulfate -initiated polymerizations together with electrospray mass spectrometry of aqueous phase oligomers, has shown that the mechanism for the induced decomposition of persulfate by vinyl acetate is chain transfer to initiator from aqueous-phase oligomeric radicals. A value has been determined for the rate coefficient for transfer to initiator, by fitting literature data to a model based on this mechanism. The reported independence of the rate of polymerization from the monomer concentration in the emulsion polymerization of vinyl acetate has been investigated. Possible explanations for this behaviour have been proposed and tested in this work, by measuring radical-loss rates directly with y-relaxation techniques. Although the Y relaxations were found to be affected by experimental artefacts, it has been demonstrated that rapid exit is not responsible for the high radical-loss rates in this system. The major artefact identified in the y relaxations was the significant effect of relatively small exotherms on relaxation behaviour, Methodologies were developed for correcting affected data and for avoiding exotherms under certain conditions. Arrhenius parameters were determined for the rate coefficient for chain transfer to monomer using the In^M method, which utilises the whole MWD. This section of the work is incomplete, for reasons detailed in chapter 5. However, as a preliminary indication it was found that the frequency factor was 106.38 M-1 s-1 and the activation energy was 38.8 kJ mol-1.
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De, Bruyn Hank. "The Emulsion Polymerization of Vinyl Acetate." University of Sydney, Chemistry, 1999. http://hdl.handle.net/2123/381.

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Abstract This work investigates the kinetics of the emulsion polymerization of vinyl acetate. Several aspects of this system have been clarified, including the induced decomposition of persulfate, retardation by oxygen and entry by, and analysis of, the aqueous phase oligomeric radicals. It has been shown that the retardation period observed in the emulsion polymerization of VAc can be explained by the effect of traces of oxygen (< 10-6 M) on the entry efficiency of the initiator-derived aqueous-phase oligomeric radicals. Comparison of rates of polymerization in V and persulfate -initiated polymerizations together with electrospray mass spectrometry of aqueous phase oligomers, has shown that the mechanism for the induced decomposition of persulfate by vinyl acetate is chain transfer to initiator from aqueous-phase oligomeric radicals. A value has been determined for the rate coefficient for transfer to initiator, by fitting literature data to a model based on this mechanism. The reported independence of the rate of polymerization from the monomer concentration in the emulsion polymerization of vinyl acetate has been investigated. Possible explanations for this behaviour have been proposed and tested in this work, by measuring radical-loss rates directly with y-relaxation techniques. Although the Y relaxations were found to be affected by experimental artefacts, it has been demonstrated that rapid exit is not responsible for the high radical-loss rates in this system. The major artefact identified in the y relaxations was the significant effect of relatively small exotherms on relaxation behaviour, Methodologies were developed for correcting affected data and for avoiding exotherms under certain conditions. Arrhenius parameters were determined for the rate coefficient for chain transfer to monomer using the In^M method, which utilises the whole MWD. This section of the work is incomplete, for reasons detailed in chapter 5. However, as a preliminary indication it was found that the frequency factor was 106.38 M-1 s-1 and the activation energy was 38.8 kJ mol-1.
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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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Tongcher, Oychai. "Novel routes to stereoregular poly(vinyl acetate)." Thesis, University of Cambridge, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.620688.

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Cauich-Rodriguez, Juan Valerio. "Hydrogels based on poly(vinyl alcohol-vinyl acetate) blends for biomedical applications." Thesis, Queen Mary, University of London, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.267577.

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Kumar, Dheeraj. "Synthesis of vinyl acetate on palladium-based catalysts." [College Station, Tex. : Texas A&M University, 2006. http://hdl.handle.net/1969.1/ETD-TAMU-1747.

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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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Haley, Roger David. "Surface chemistry of the vinyl acetate catalytic system." Thesis, University of Cambridge, 1999. https://www.repository.cam.ac.uk/handle/1810/272089.

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Books on the topic "Vinyl acetate"

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United States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Vinyl acetate. Atlanta, GA: Agency for Toxic Substances Disease Registry, Division of Toxicology, Dept. of Health and Human Services, Public Health Service, 1992.

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United States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Acetato de vinilo. Atlanta, GA]: Agencia para Sustancias Tóxicas y el Registro de Enfermedades, División de la Toxicología, Departamento de Salud y Servicios Humanos de los EE.UU., Servicio de Salud Pública, 1992.

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Vinyl acetate emulsion polymerization and copolymerization with acrylic monomers. Boca Raton, Fla: CRC Press, 2000.

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

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J, Strauss Robert. Polyvinyl acetate adhesives for double-fan adhesive binding: Report on a review and specification study. [Edina, Minn: Library Binding Institute], 1992.

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Institute, Library Binding, ed. Long-term service life and performance characteristics of the PVA cold emulsion adhesives used for the double fanning process in library binding: Are PUR adhesives a viable alternative? [Rochester, N.Y.]: Library Binding Institute, 1991.

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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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Hayes, Teresa L., Robyn Margulies, and Debra A. Celinski. Acetic acid & derivatives. Cleveland: Freedonia Group, 2000.

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Canadian Conservation Institute. Conservation Research Services and Canada Communications Canada, eds. Adhesive testing at the Canadian Conservation Institute: An evaluation of selected poly(vinyl acetate) and acrylic adhesives. Ottawa, Canada: Communications Canada, 1992.

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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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Book chapters on the topic "Vinyl acetate"

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Bährle-Rapp, Marina. "Vinyl Acetate." In Springer Lexikon Kosmetik und Körperpflege, 583. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_11036.

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Gooch, Jan W. "Vinyl Acetate." In Encyclopedic Dictionary of Polymers, 794. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_12539.

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Gooch, Jan W. "Vinyl Acetate Plastics." In Encyclopedic Dictionary of Polymers, 794. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_12540.

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Gooch, Jan W. "Poly(vinyl acetate co vinyl chloride)." In Encyclopedic Dictionary of Polymers, 576. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9253.

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Steiner, G., and C. Zimmerer. "Poly(vinyl acetate) (PVAC)." In Polymer Solids and Polymer Melts – Definitions and Physical Properties I, 1020–26. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-32072-9_116.

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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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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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Wohlfarth, Ch. "Viscosity of vinyl acetate." In Supplement to IV/18, 201. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_93.

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Wohlfarth, Christian. "Viscosity of vinyl acetate." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures, 101. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_88.

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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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Conference papers on the topic "Vinyl acetate"

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Desai, Umang, Bhuwanesh Kumar Sharma, and Aparna Singh. "Vinyl acetate content tailoring in ethylene vinyl acetate improves the resilience against environmental stressors." In 2022 IEEE 49th Photovoltaics Specialists Conference (PVSC). IEEE, 2022. http://dx.doi.org/10.1109/pvsc48317.2022.9938499.

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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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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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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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Kolesniková, Lucie, Isabelle Kleiner, Jose Cernicharo, José Alonso, and Isabel Peña. "THE MILLIMETER-WAVE SPECTRUM OF VINYL ACETATE." In 69th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.rj05.

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Agroui, K., and N. Benrekaa. "Characterisation of etylene vinyl acetate for photovoltaic application." In Proceedings of International Conference on Microelectronics (ICM'99). IEEE, 2000. http://dx.doi.org/10.1109/icm.2000.884856.

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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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Liu, Chengcen, Tao Dou, Feng Qiu, Jiangao Yang, and Kai Shi. "Study on the Stability of Poly(Vinyl Alcohol)/Poly(Vinyl Acetate) Electrothermal Membrane." In 2010 4th International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2010. http://dx.doi.org/10.1109/icbbe.2010.5516568.

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hu, yingmo. "Preparation and Characterization of Tourmaline Tetradecenylsuccinate- Vinyl Acetate Copolymer." In International Conference on Nanomaterials, Functional and Composite Materials. HKIRIT, 2018. http://dx.doi.org/10.24177/ckconf2017050002.

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Jing, Yang, Zeng Hui, and Huang Jiangping. "Vinyl Acetate Polymerization Rate Prediction Based on FOA GNN." In 2014 Ninth International Conference on P2P, Parallel, Grid, Cloud and Internet Computing (3PGCIC). IEEE, 2014. http://dx.doi.org/10.1109/3pgcic.2014.61.

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Toxqui-Lopez, S., A. Olivares-Pérez, V. Santacruz-Vazquez, I. Fuentes-Tapia, and J. Ordoñez-Padilla. "UV recording with vinyl acetate and muicle dye film." In SPIE OPTO, edited by Hans I. Bjelkhagen and V. Michael Bove. SPIE, 2015. http://dx.doi.org/10.1117/12.2079712.

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Reports on the topic "Vinyl acetate"

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Richard D. Colberg, Nick A. Collins, Edwin F. Holcombe, Gerald C. Tustin, and Joseph R. Zoeller. Alternate fuels and chemicals from synthesis gas: Vinyl acetate monomer. Final report. Office of Scientific and Technical Information (OSTI), January 1999. http://dx.doi.org/10.2172/750388.

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Stern, S. A. Mechanisms of gas permeation through polymer membranes: Summary technical report, January 1986--December 1989. [Poly(alkyl methacrylates), poly-(1-trimethylsylil-1-propyne), and poly(vinyl acetate)]. Office of Scientific and Technical Information (OSTI), January 1989. http://dx.doi.org/10.2172/6182255.

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