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Difunctional monomers, stability

The properties of these varnishes first of all depend on the parent monomers. As we have mentioned above, the production of varnishes can be based on both difunctional monomers (e.g. dimethyl- or methyl-phenyldichlorosilane) and trifunctional monomers (methyltrichlorosilane, phenyltrichlorosilane, etc). As the content of difunctional monomer in a mixture of organochlorosilanes increases, the varnish film becomes more elastic however, its hardness decreases and the time of transition into the nonmeltable and nonsoluble state is reduced. Increasing the trifunctional monomer content (phenyltrichlorosilane) in the mixture increases thermal stability and gloss of the film) at the same time, the time of transition into the nonmeltable and nonsoluble state is greatly increased in comparison with varnishes containing methylsisequioxane elements. [Pg.309]

Polyindanes have been obtained from a variety of monomers which are capable of forming benzyl carbenium ions stabilized with dialkyl groups upon the appropriate initiation. Linear polymers containing indane units in the main chain have been obtained by the BClj-initiated polymerization of 1,4-diisopropenylbenzene [Eq. (6)] [8]. Polyindanes with structural unit IS have also been obtained when difunctional monomers capable of forming a,a-dimethylbenzylic carbenium ions upon treatment with an initiator [8-12] (Fig. 4). [Pg.561]

Physical properties of the polyethylene were, in general, improved. The use of the difunctional monomer resulted in better dimensional stability at 185°C (a combination of 1.2 Mrad with 4% monomer being equivalent to a dose of 30 Mrad without monomer addition) and in improved tensile strength. [Pg.225]

A pellicular chromatographic packing consists of a rigid core with a relatively thick outer shell. The outer shell is cross-linked by the inclusion of a difunctional monomer and for added stability the outer shell may be covalently attached to the core. An example of this type of packing is the material developed for carbohydrate analysis, CarboPac (Dionex), which is a pellicular anion exchange resin bead which has a 5 pm non-porous sulphonated polystyrene bead core with a 0.1 pm quaternary amine latex. These materials have gained widespread acceptance for analytical separations and small-scale fractionations. [Pg.108]

An alternative route to polybenzazoles was devised, by polymerizing dinitro difunctional nucleophilic monomers with terephthaloyl chloride, followed by reduction of the nitro groups and cyclization [35], This approach has the advantage of oxidative stability of the dinitro monomers complete conversion in reduction and cyclization are unlikely to be easily achieved. [Pg.122]

The principal monomers butadiene, styrene, vinyl acetate, (meth)acrylates and acrylonitrile essenhally determine the material properties of films made from the corresponding dispersions the glass transition temperature, the water absorption capacity, the elasticity, etc. Auxiliary monomers, which are only used in a small proportion, usually <5 %, control important properties such as colloid-chemical stabilization (acrylic acid, methacrylic acid, acrylamide, methacrylamide), crosslinking within the particles (difunctional acrylates, divinylbenzene, etc.) or hydrophilic properties (OH-containing monomers, such as hydroxyacrylates). Reactive monomers which still contain a latently reactive group even after incorporation into the polymer, for example glycidylmethacrylate or N-methylol(meth)acrylamide, can form a network between various particles and polymer molecules after film formation. [Pg.9]


See other pages where Difunctional monomers, stability is mentioned: [Pg.1653]    [Pg.103]    [Pg.341]    [Pg.519]    [Pg.392]    [Pg.319]    [Pg.550]    [Pg.109]    [Pg.6660]    [Pg.258]    [Pg.199]    [Pg.458]    [Pg.210]    [Pg.151]    [Pg.178]    [Pg.185]    [Pg.1281]    [Pg.322]    [Pg.32]    [Pg.979]    [Pg.138]    [Pg.290]    [Pg.127]    [Pg.6676]    [Pg.36]    [Pg.2239]    [Pg.105]   
See also in sourсe #XX -- [ Pg.519 ]




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