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Vinyl acetate

About: Vinyl acetate is a research topic. Over the lifetime, 15970 publications have been published within this topic receiving 162142 citations. The topic is also known as: Ethenyl acetate & Ethenyl ethanoate.


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Journal ArticleDOI
TL;DR: This is the first example of alternating copolymerization of a polar vinyl monomer and carbon monoxide using vinyl acetate using palladium catalysts with phosphine−sulfonate bidentate ligands and the first nonradical pathway for polymer synthesis with Vinyl acetate.
Abstract: We report the first example of alternating copolymerization of a polar vinyl monomer and carbon monoxide using vinyl acetate. Alternating copolymers with high molecular weights were prepared employing palladium catalysts with phosphine−sulfonate bidentate ligands. NMR and MALDI-TOF MS analyses revealed that the obtained materials were alternating copolymers of vinyl acetate and carbon monoxide. This is also the first nonradical pathway for polymer synthesis with vinyl acetate, one of the most inexpensive and readily available polar vinyl monomer, as a major component.

72 citations

Journal ArticleDOI
Li Liu1, Yong Wang1, Yanli Li1, Jun Wu1, Zuowan Zhou1, Chongxi Jiang1 
03 Jul 2009-Polymer
TL;DR: In this paper, functionalized multiwalled carbon nanotubes (f-MWCNTs) have been introduced into immiscible polypropylene/ethylene- co-vinyl acetate (PP/EVA) blends.

72 citations

01 Jan 2007
TL;DR: In this article, the effect of various solutions such as water, ethylacetate, acetonitrile, methylacetate and surface active agents on the properties of polypyrrole and its composites were studied.
Abstract: Polypyrrole and its composites were prepared chemically using FeCl3 as an oxidant in aqueous and non-aqueous media. The effect of various solutions such as water, ethylacetate, acetonitrile, methylacetate, methanol, ethylmethylketone and surface active agents, poly (ethylene glycol) and poly (vinyl acetate) on the properties of pro duct were studied. The electrically conducting polymer and its composites have been characterized by Scanning Electron Microscopy (SEM), Fourier Transform Infrared (FTIR) and proton nuclear magnetic resonance ( 1 H NMR) spectroscopy. The results indicate that the morphology, conductivity and structure of products are dependent on the type of solution and additive.

71 citations

Journal ArticleDOI
TL;DR: In this paper, the authors investigated the grafting of polymers having pendant peroxycarbonate groups onto ultrafine silica surface and the radical postgraft polymerization of vinyl monomers initiated by the initiating groups of polymer chains grafted onto the surface.
Abstract: The grafting of polymers having pendant peroxycarbonate groups onto ultrafine silica surface and the radical postgraft polymerization of vinyl monomers initiated by the initiating groups of polymer chains grafted onto silica surface were investigated. The grafting of polymers having pendant peroxycarbonate groups onto the silica surface was achieved by the copolymerization of vinyl acetate (VAc) with t-butylperoxy-2-methacryloyloxyethylcarbonate (HEPO) initiated by azo groups introduced onto silica surface: the introduction of azo groups onto silica surface was achieved by the reaction of 4,4′-azobis(4-cyanopentanoic acid) with amino groups previously introduced onto the surface. The percentage of grafting (the proportion of grafted polymer to silica) of poly(VAc–co-HEPO) onto the surface was about 51% at 80.0°C after 3 h. The amount of pendant peroxycarbonate groups of grafted chain was determined to be 0.55 mmol/g. Radical postgraft polymerization of various vinyl monomers, such as methyl methacrylate, glycidyl methacrylate, 2-hydroxyethyl methacrylate, vinyl acetate, and N-vinyl-2-pyrrolidinone was initiated by the pendant peroxycarbonate groups of grafted poly(VAc–co-HEPO) to give the corresponding hyperbranched polymer-grafted silica. It was found that the grafting of hydrophilic or hydrophobic polymers readily controls the surface wettability to water.

71 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202389
2022142
2021157
2020199
2019277
2018351