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Статті в журналах з теми "Vinyle Acetate"
Grenier-Loustalot, M. F., M. Audenaert, J. Boutillier, and D. Lecacheux. "Etude structurale (sequence, tacticite, branchement alkyl) de copo ethylene, acrylate d'hydroxyethyle et acetate de vinyle par RMN 1H et 13C haute resolution dans les liquides." European Polymer Journal 25, no. 4 (1989): 411–18. http://dx.doi.org/10.1016/0014-3057(89)90159-6.
Повний текст джерелаФилатов, И. Е., В. В. Уварин та Д. Л. Кузнецов. "Исследование относительной реакционной способности паров алкилацетатов по отношению к компонентам плазмы импульсного разряда в воздухе". Письма в журнал технической физики 49, № 11 (2023): 25. http://dx.doi.org/10.21883/pjtf.2023.11.55534.19540.
Повний текст джерелаJung, 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.
Повний текст джерелаGonzález, Cristina, Jose Ma Resa, Juan Lanz, and Jose A. Mtz de Ilarduya. "Excess molar volumes of binary mixtures containing vinyl acetate + alkyl acetates at 298.15 K. Anomalous behavior of methyl acetate + vinyl acetate mixtures." Fluid Phase Equilibria 137, no. 1-2 (November 1997): 141–48. http://dx.doi.org/10.1016/s0378-3812(97)00083-6.
Повний текст джерелаBui, 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.
Повний текст джерелаO'Neill, Mark L., Deborah Newman, Eric J. Beckman, and Steve P. Wilkinson. "Solvent-free generation of poly(vinyl acetals) directly from poly(vinyl acetate)." Polymer Engineering & Science 39, no. 5 (May 1999): 862–71. http://dx.doi.org/10.1002/pen.11475.
Повний текст джерелаMyshak, 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.
Повний текст джерелаHe, Chen, Qin Gao, Changwen Ye, Guotao Yang, Pengfei Zhang, Rongchao Yang, Qing Zhang, and Kang Ma. "Development of a Purity Certified Reference Material for Vinyl Acetate." Molecules 28, no. 17 (August 25, 2023): 6245. http://dx.doi.org/10.3390/molecules28176245.
Повний текст джерелаBolt, Hermann. "Vinyl acetate." Toxicology 226, no. 1 (September 2006): 19. http://dx.doi.org/10.1016/j.tox.2006.05.030.
Повний текст джерелаLuttrell, 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.
Повний текст джерелаДисертації з теми "Vinyle Acetate"
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.
Повний текст джерелаMorel, Aurélie. "Synthèse et comportement auto-associatif des copolymères poly(acetate de vinyle)-b-poly(acide acrylique) et de leurs dérivés hydrolysés." Montpellier 2, 2004. http://www.theses.fr/2004MON20162.
Повний текст джерелаDhuiège, Benjamin. "Acylation des nanocelluloses en milieu aqueux par transestérification des esters de vinyle et utilisation comme charge dans le caoutchouc naturel." Thesis, Bordeaux, 2017. http://www.theses.fr/2017BORD0645/document.
Повний текст джерелаThe objective of this research work consists in the elaboration of novel composite materials (elastomers, adhesives) using nanocelluloses (CNC and NFC) as biobased reinforcing fillers. A method allowing the functionalization of nanocelluloses in aqueous conditions was first developed, with the aim of ultimately improving their compatibility with polymer matrices. The reaction, based on the transesterification of vinyl esters, was optimized with vinyl acetate selected as model reactant. The grafting performed in basic aqueous conditions was efficient, but also led to the formation of poly(vinyl acetate) as a by-product. To limit this problem, a second protocol in neutral aqueous conditions was also developed, but lower yields were obtained in that case. The unmodified and acetylated nanocelluloses were then dispersed in a natural rubber matrix (NR), to study the impact of this filler on the thermomechanical performances of the crude and vulcanized material. An improvement of the mechanical properties was observed in the presence of NCC or NFC, but the acetylation of the nanoparticles did not enhance further the performances. Finally, a valorization of the PVAc produced during the acetylation of the nanocelluloses in basic aqueous conditions was proposed. The dispersion of the acetylated NCC in the PVAc polymerized in-situ indeed led to the production of composites with improved properties. The subsequent utilization of these composites as filler (master batch) in NR or EVA matrices was discussed
Atanase, Léonard-ionut. "Contribution à l'étude des complexes Poly (vinyle alcool - vinyle acétate) / tensioactifs anioniques : caractéristiques colloïdales des nanogels et extension aux copolymères à blocs." Thesis, Mulhouse, 2010. http://www.theses.fr/2010MULH3728.
Повний текст джерелаPoly (vinyl acetate-co-vinyl alcohol) copolymers, designated by PVA, are macromolecular surfactants obtained by partial hydrolysis of poly (vinyl acetate) (PVAc). If the surfactant properties of PVA have been correlated with molecular characteristics it is not the same for the colloidal aggregates in aqueous solutions so-called nanogels. The objective of this thesis was to characterize the nanogels using techniques such as dynamic light scattering, size exclusion chromatography and viscometry.9 PVA with degrees of hydrolysis between 73 and 88 mole% and polymerization degrees of 650 to 2500 were studied. It appeared that the nanogels, formed by hydrophobic-hydrophobic interactions between acetate sequences, are the size in the range of 20 to 40 nm with volume fractions between 20 and 30%. The disaggregation of nanogels by complex formation with anionic surfactants such as SDS and SDBS was further demonstrated. By using the "cloud point" fractionation technique it appeared that SDS is complexed by the sequences with high acetate content and in particular those with significant lengths of acetate sequences.As a model system diblock copolymers PVAc-b-PVOH containing a PVAc hydrophobie sequence and a PVOH hydrophilic sequence were prepared by RAFT polymerization, followed by a click reaction. A preliminary micellization study of these copolymers showed a very strong analogy between PVAc-b-PVOH block copolymer micelles and PVA nanogels discussed above
Dommanget, Cédric. "Polymérisation radicalaire contrôlée : le défi de l'éthylène." Thesis, Lyon 1, 2013. http://www.theses.fr/2013LYO10216/document.
Повний текст джерелаThe 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)
Atanase, Léonard-Ionut. "Contribution à l'étude des complexes Poly (vinyle alcool - vinyle acétate) / tensioactifs anioniques : caractéristiques colloïdales des nanogels et extension aux copolymères à blocs." Phd thesis, Université de Haute Alsace - Mulhouse, 2010. http://tel.archives-ouvertes.fr/tel-00562063.
Повний текст джерелаPalma, Mauri Sergio Alves. "Polimerização de acetato de vinila em emulsão de modo contínuo em coluna pulsada de pratos perfurados." Universidade de São Paulo, 2002. http://www.teses.usp.br/teses/disponiveis/3/3137/tde-27082013-122010/.
Повний текст джерелаIndustrial emulsion polymerization processes are usually carried out in stirred tanks operated in batch/semibatch or in continuous mode (CSTR). In comparison to batch processes, continuous reactors present several advantages such as lower volumes and better quality control by reducing batch-to-batch variations. Continuous emulsion polymerization in CSTR may exhibit sustained oscillations in conversion, particle size and particle concentration. Such oscillations may be reduced in pulsed tubular reactors due to less axial mixing. In this thesis a new type of tubular reactor, called Pulsed Sieve Plate Column, PSPC, was developed for the continuous process of vinyl acetate emulsion polymerization. This reactor is operated using oscillatory pulsed flow and uses perforated plates as internals. Residence time distribution runs were carried out in a glass reactor in order to characterize the axial mixing and flow patterns in the PSPC. The data were treated using the axially dispersed plug flow model. Axial dispersion coefficient was measured for different conditions of pulse frequency and amplitude, flow rate, plate spacing and viscosity. It was found that the degree of axial mixing can be varied in wide ranges by manipulating pulsation frequency and/or amplitude. Vinyl acetate continuous emulsion polymerization runs were carried out in a jacketed stainless steel reactor (with the same size of the glass reactor). Monomer conversion and particle size distribution was measured both at the reactor exit in transient state and along the reactor length at steady-state. It was found that average residence time and degree of axial mixing affect process and product quality variables, such as monomer conversion, mean particle size and concentration, but did not affect the viscosity of the emulsion produced, for the recipe and conditions used. A mathematical model for the reactor was developed. The model used, based on a well-known kinetic model previously developed in the literature for batch emulsion polymerization, was adapted to the continuous tubular reactor by adding the dispersion and convective terms to the balance equations. The model was numerically solved. Only two parameters were adjusted in this model and the simulated results showed excellent agreement with the experimental results, for steady state conditions. The proposed tubular reactor allows to reach high monomer conversion with similar or even lower residence time than those in batch processes and reaches steady state operation in just one to two mean residence times. The reactor is efficient, easy-to-built, easy-to-clean, robust and promising for use in industrial continuous emulsion polymerization of vinyl acetate.
Hashimoto, Patrícia Kazuyo. "Complexos de Mn(II) e Fe(II) coordenados a bases de Schiff Bidentadas derivadas de cicloalquilaminas como mediadores da OMRP de acetato de vinila /." Presidente Prudente, 2018. http://hdl.handle.net/11449/154400.
Повний текст джерелаCoorientador: Valdemiro Pereira de Carvalho Júnior
Banca: Pedro Ivo da Silva Maia
Banca: Ana Maria Pires
Resumo: Nas últimas décadas, a polimerização radicalar controlada (CRP) tem se tornado muito importante, pois permite a síntese de macromoléculas de arquiteturas específicas com um controle sobre as propriedades químicas e físicas. Sendo assim, este trabalho apresenta a síntese de novos complexos de Mn(II) e Fe(II) coordenados à ligantes bases de Schiff bidentados, que são resultantes da condensação do salicilaldeído com as seguintes cicloalquilaminas: (1) Ciclopentilamina, (2) Cicloexilamina, (3) Cicloeptilamina e (4) Ciclooctilamina, de forma que estes possam ser utilizados como mediadores da polimerização radicalar mediada por organometálicos. Os ligantes foram caracterizados pelas seguintes técnicas: espectroscopia de ressonância magnética nuclear de hidrogênio (RMN de 1H), espectroscopia de absorção na região do ultravioleta-visível (UV-Vis) e espectroscopia vibracional na região do infravermelho (FTIR). Já os complexos de Mn(II) e Fe(II) foram caracterizados pelas técnicas de FTIR, UV-Vis, voltametria cíclica (VC) e ponto de fusão (p.f.). Os estudos cinéticos de polimerização foram realizados para os complexos de manganês e ferro. O complexo [MnIIbis(N-Salicilideno-Ciclopentilamina)], Mn(L1)2, apresentou um melhor controle na polimerização do acetato de vinila com menores valores de polidispersidade e a curva de massa molecular (Mn) mais próxima aos valores da curva teórica. Já os complexos de ferro mediadores apresentaram um comportamento mais similar, não havendo muita...
Abstract: In the last decades, controlled radical polymerization (CRP) has become very important, since it facilitates the synthesis of macromolecules of specific architectures with excellent control over the chemical and physical properties. Thus, this work presents the synthesis of new Mn(II) and Fe(II) complexes coordinated with the bidentate Schiff bases ligands, which are the result of the condensation of salicylaldehyde with cycloalkylamines: (1) cyclopentylamine, (2) cyclohexylamine, (3) cycloheptylamine and (4) cyclooctylamine, so that they can be used as mediators of radical polymerization mediated by organometallic (OMRP). The ligands synthesized were characterized by proton nuclear magnetic resonance (1H-NMR) spectroscopy, ultraviolet-visible (UV-Vis) absorption spectroscopy and Fourier-transform infrared spectroscopy (FTIR) techniques. The synthesized Mn(II) and Fe(II) complexes were studied by FTIR, UV-Vis, cyclic voltammetry (CV) and melting point (m.p.). Kinetic polymerization studies were performed for the manganese and iron complexes. The [MnIIbis (N-Salicylidene-Cyclopentylamine)], Mn(L1)2, complex showed a better control in the polymerization of vinyl acetate with lower values of polydispersity and the molecular mass curve (Mn) closer to the values of the theoretical curve. However, the iron mediator complexes presented a more similar behavior, not having much difference in the kinetic curves
Mestre
Raihane, Mustapha. "Copolymérisation du méthyl cyanure de vinylidène (MVCN) avec l'acétate de vinyle et des styrènes substitués : synthèses, microstructures, propriétés et dégradation thermique." Saint-Etienne, 1993. http://www.theses.fr/1993STET4017.
Повний текст джерелаFranco, Cilene Meinberg. "Pesquisa experimental sobre a polimerização via radical livre com iniciadores mono e difuncional." [s.n.], 2006. http://repositorio.unicamp.br/jspui/handle/REPOSIP/266156.
Повний текст джерелаDissertação (mestrado) - Universidade Estadual de Campinas. Faculdade de Engenharia Quimica
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Resumo: Iniciadores mono funcionais são largamente utilizados em polimerizações VIa radical livre. Muitas vezes, na busca de maiores produtividades, utilizam-se temperaturas de operação mais elevadas e/ou maiores concentrações iniciais de iniciador, que por conseqüência, geram polímeros com pesos moleculares mais baixos. O uso de iniciadores difuncionais permite o aumento da produtividade sem a redução no peso molecular do produto final, o que pode ser urna característica desejável. A pesquisa com iniciadores difuncionais é atual e de grande interesse industrial. O objetivo deste trabalho é analisar o efeito da funcionalidade do iniciador, no caso mono e difuncional, sobre a polimerização via radical livre, considerando corno caso estudo um polímero linear, o poliestireno, e um ramificado, o poli (acetato de vinila). Para isso, foram feitas, experimentalmente, reações de polimerização em ampolas de vidro (polimerização em massa), com o iniciador mono funcional (Luperox TBEC) e o di funcional (Luperox 531). Foram analisados também o efeito da temperatura de polimerização e a concentração de iniciador. Também neste trabalho é apresentado um estudo estatístico através de um Planejamento Fatorial, a fim de analisar o efeito das variáveis temperatura e concentração de iniciador na polimerização do estireno com iniciador difuncional. Observou-se, tanto para o estireno corno para o acetato de vinila, que quando utilizado o iniciador difuncional é possível obter conversões maiores, sem alterar o peso molecular médio mássico e numérico, sendo que em alguns casos pode se até obter um aumento no peso molecular. O uso de iniciador di funcional é também mais viável economicamente, pois apresenta melhores resultados frente ao monofuncional, mesmo quando utilizado em concentrações ou temperaturas menores do que as utilizadas com o iniciador mono funcional. É importante salientar o caráter inovador desta pesquisa, já que não foram encontrados, em literatura aberta, dados experimentais da polimerização do acetato de vinila (ou outro monômero que produza ramificações de cadeia longa) utilizando iniciadores difuncionais
Abstract: Monofunctional initiators are extensively utilized in free radical polymerization. In order to increase productivity, higher temperature or higher initial initiator concentration are used, therefore polymers with lower molecular weights are obtained. Bifunctional initiators increase the polymerization rate without decreasing the average molecular weight and this can be desirable. They are an important issue to be investigated and are of great interest to industries. The objective of this work is to analyze the effect of the functionality of the initiator, by using mono and bifunctional, in free radical polymerization, for linear polymer (poly styrene) and branched polymer (poly(vinyl acetate)). Polymerizations were experimentally performed in glass ampoules (bulk polymerization) using both mono(Luperox TBEC) and bi- (Luperox 531) functional initiators. The effects of temperature and initiator concentration were also analyzed for various polymerization conditions. This work includes a statistical study using the factorial design to analyze the effect of temperature and initiator concentration in styrene polymerization with bifunctional initiator. It is observed in this study, that high conversions with no effect in the molecular weigh of the dead polymer can be achieved using bifunctional initiators in the polymerization of styrene and vinyl acetate. In many cases, it is possible to obtain higher molecular weights. Bifunctional initiator can also be used to provide reduction costs to initiators. They showed better results than the monofunctional initiator when lower concentration or temperature lower were utilized.
Mestrado
Desenvolvimento de Processos Químicos
Mestre em Engenharia Química
Книги з теми "Vinyle Acetate"
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.
Знайти повний текст джерелаUnited 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.
Знайти повний текст джерелаJ, Strauss Robert. Polyvinyl acetate adhesives for double-fan adhesive binding: Report on a review and specification study. [Edina, Minn: Library Binding Institute], 1992.
Знайти повний текст джерелаVinyl acetate emulsion polymerization and copolymerization with acrylic monomers. Boca Raton, Fla: CRC Press, 2000.
Знайти повний текст джерелаClarke, S. D. The characterization of ethylene-vinyl acetate copolymers. Wolverhampton: University ofWolverhampton, 1993.
Знайти повний текст джерелаInstitute, 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.
Знайти повний текст джерелаKhunniteekool, Chonlada. Structure/property relationships of cross-linked polyethylene and ethylene vinyl acetate copolymer foams. Manchester: UMIST, 1995.
Знайти повний текст джерелаHayes, Teresa L., Robyn Margulies, and Debra A. Celinski. Acetic acid & derivatives. Cleveland: Freedonia Group, 2000.
Знайти повний текст джерелаCanadian 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.
Знайти повний текст джерелаInstitute, 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.
Знайти повний текст джерелаЧастини книг з теми "Vinyle Acetate"
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.
Повний текст джерелаGooch, 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.
Повний текст джерелаGooch, 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.
Повний текст джерелаGooch, 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.
Повний текст джерелаSteiner, 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.
Повний текст джерелаBashford, 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.
Повний текст джерелаWhelan, 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.
Повний текст джерелаWohlfarth, 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.
Повний текст джерелаWohlfarth, 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.
Повний текст джерелаGooch, 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.
Повний текст джерелаТези доповідей конференцій з теми "Vinyle Acetate"
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.
Повний текст джерелаIzutsu, 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.
Повний текст джерелаShady, 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.
Повний текст джерелаKolesniková, 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.
Повний текст джерелаAgroui, 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.
Повний текст джерелаKempe, 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.
Повний текст джерелаLiu, 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.
Повний текст джерелаhu, 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.
Повний текст джерелаJing, 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.
Повний текст джерелаToxqui-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.
Повний текст джерелаЗвіти організацій з теми "Vinyle Acetate"
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.
Повний текст джерелаMeier, Rico. Ultrasonic Characterization of Ethylene Vinyl Acetate (EVA) Crosslinking for Quality Assurance and Lamination Process Control (US-Xlink). Office of Scientific and Technical Information (OSTI), November 2021. http://dx.doi.org/10.2172/1969746.
Повний текст джерелаStern, 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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