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Vinyl ether monomers

Vinyl ether monomers and polymers, AJ-Vinylamide polymers. [Pg.448]

One class of materials with some inherent PSA properties includes polyvinyl-ethers. Vinyl ether monomers are industrially derived from the reaction of acetylene with alcohols [117]. The most common alcohols used are methanol, ethanol or isobutanol. A generic structure of the vinyl ether is shown below ... [Pg.509]

Vinyl ethers constitute a third class of monomers which have been cationically polymerized in C02. While fluorinated vinyl ether monomers such as those described in Sect. 2.1.2 can be polymerized homogeneously in C02 because of the high solubility of the resulting amorphous fluoropolymers, the polymerization of hydrocarbon vinyl ethers in C02 results in the formation of C02-insoluble polymers which precipitate from the reaction medium. The work in this area reported to date in the literature includes precipitation polymerizations and does not yet include the use of stabilizing moieties such as those described in the earlier sections on dispersion and emulsion polymerizations (Sect. 3). [Pg.131]

The objective of the present work was to determine the influence of the light intensity on the polymerization kinetics and on the temperature profile of acrylate and vinyl ether monomers exposed to UV radiation as thin films, as well as the effect of the sample initial temperature on the polymerization rate and final degree of cure. For this purpose, a new method has been developed, based on real-time infrared (RTIR) spectroscopy 14, which permits to monitor in-situ the temperature of thin films undergoing high-speed photopolymerization, without introducing any additive in the UV-curable formulation 15. This technique proved particularly well suited to addressing the issue of thermal runaway which was recently considered to occur in laser-induced polymerization of divinyl ethers 13>16. [Pg.64]

Alkenyloxystyrene monomers such as 4-allyloxystyrene are useful components of photocured cationically polymerizable compositions. Used alone or in combination with divinyl ethers they provide low viscosity formulations, which are excellent solvents for commercial onium salt photoinitiators. Photocuring rates are comparable to vinyl ether monomers and the initially photocured alkenyloxystyrene polymers may be further heat processed to yield crosslinked phenolic type resins having outstanding thermal resistance properties. The new materials have good adhesive properties and are potentially useful where a combination of ease of processability and high performance is required. [Pg.119]

The hydroxylated vinyl ether monomers can be further fuctionalized on the hydroxy group. For example, the conversion of 5 to its various derivatives 16-20 is straightforwad, and thus provides the entry to new difunctional fluorinated monomers.23... [Pg.61]

Table 13.2. Copolymerization of (S02F)-Functional Perfluorinated Alkyl Vinyl Ether Monomer with TFE... Table 13.2. Copolymerization of (S02F)-Functional Perfluorinated Alkyl Vinyl Ether Monomer with TFE...
Epoxy-functional polydimethylsiloxane oligomers are another group that can be cured by UV radiation. Epoxysilicone block copolymers exhibit a good photoinitiator miscibility, high cure rate, and compatibility with epoxy and vinyl ether monomers. These block copolymers form flexible films with excellent release properties and are therefore used as release coatings. ... [Pg.78]

See Vinyl POLYMERS, VINYL ETHER MONOMERS AND POLYMERS. [Pg.514]

VINYL P OLYMERS - VINYL ETHER MONOMERS AND POLYMERS] (Vol 24)... [Pg.11]


See other pages where Vinyl ether monomers is mentioned: [Pg.1054]    [Pg.514]    [Pg.514]    [Pg.515]    [Pg.516]    [Pg.516]    [Pg.516]    [Pg.517]    [Pg.517]    [Pg.518]    [Pg.519]    [Pg.520]    [Pg.520]    [Pg.521]    [Pg.223]    [Pg.71]    [Pg.77]    [Pg.195]    [Pg.197]    [Pg.201]    [Pg.195]    [Pg.197]    [Pg.201]    [Pg.533]    [Pg.576]    [Pg.615]    [Pg.784]    [Pg.785]    [Pg.786]   


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