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Copolymerization Effects

Copolymerization effect (also referred to as the "copolymer effect") related to the change of... [Pg.256]

If desired, the copolymerization effect of crosslinking can also be taken into account by using Equation 6.16, via the possible dependences of Tg(°°) and Nrot on the composition. [Pg.258]

When crosslinking was accomplished by reacting monomers which incorporated repeat units of different Nrot into the polymer, the variation of Nrot with composition (a manifestation of the copolymerization effect) was taken into account in the calculations. On the other hand, a single Tg(oo) value was used for each polymer, so that any possible copolymerization effect on... [Pg.261]

Attempts have been made to develop group contribution techniques to correlate and/or predict Tg for thermosets, mainly with data for epoxy resins of different structures [130-132], The study by Kreibich and Batzer [130] is a valuable reference, since it lists the Tg s of a large number of thermosets as a function of their molecular structures. The study by Won et al [132] attempts to distinguish carefully between the topological effect and the copolymerization effect. [Pg.263]

It is important to note that this is one of the very few cases where donor monomer-MA charge-transfer complexes are well characterized (Table 10.18), beyond composition, K value, and copolymerization effects. [Pg.401]

Vinyl-functional alkylene carbonates can also be prepared from the corresponding epoxides in a manner similar to the commercial manufacture of ethylene and PCs via CO2 insertion. The most notable examples of this technology are the syntheses of 4-vinyl-1,3-dioxolan-2-one (vinyl ethylene carbonate, VEC) (5, Scheme 24) from 3,4-epoxy-1-butene or 4-phenyl-5-vinyl-l,3-dioxolan-2-one (6, Scheme 24) from analogous aromatic derivative l-phenyl-2-vinyl oxirane. Although the homopolymerization of both vinyl monomers produced polymers in relatively low yield, copolymerizations effectively provided cyclic carbonate-containing copolymers. It was found that VEC can be copolymerized with readily available vinyl monomers, such as styrene, alkyl acrylates and methacrylates, and vinyl esters.With the exception of styrene, the authors found that VEC will undergo free-radical solution or emulsion copolymerization to produce polymeric species with a pendant five-membered alkylene carbonate functionality that can be further cross-linked by reaction with amines. Polymerizations of 4-phenyl-5-vinyl-l,3-dioxolan-2-one also provided cyclic carbonate-containing copolymers. [Pg.260]

In a more recent study, Charleux et studied the theoretical features of the activation-deactivation equilibrium in nitroxide-mediated copolymerization and applied it to the SGl-mediated copolymerization of methyl methacrylate with a low percentage of styrene (typically in the 4-9 mol.% range). They actually demonstrated that the system exhibited all the characteristics of a living/controlled polymerization, which was explained by the following features (1) the overall concentration of propagating radicals was strongly reduced by the copolymerization effect and the irreversible termination reactions undergone by the MMA/SGf system were hence slowed down (2) isolated styrene subunits were incorporated into the chains and the terminal one promoted the reversible deactivation by the SGI nitroxide and (3) the MMA penultimate unit effect enhanced deactivation of the so-formed styryl-SGf... [Pg.300]

In the last two sections we have considered—separately-the effects of resonance and polarity on copolymerization. While these concepts provide some insights into various observations, it is artificial to consider either one of them operating exclusively. In fact, resonance and polarity features are both active in most molecules. A method for merging their contributions is clearly desirable. [Pg.444]

Acrylamide copolymerizes with many vinyl comonomers readily. The copolymerization parameters ia the Alfrey-Price scheme are Q = 0.23 and e = 0.54 (74). The effect of temperature on reactivity ratios is small (75). Solvents can produce apparent reactivity ratio differences ia copolymerizations of acrylamide with polar monomers (76). Copolymers obtained from acrylamide and weak acids such as acryUc acid have compositions that are sensitive to polymerization pH. Reactivity ratios for acrylamide and many comonomers can be found ia reference 77. Reactivity ratios of acrylamide with commercially important cationic monomers are given ia Table 3. [Pg.142]

Acrylate polymerizations are markedly inhibited by oxygen therefore, considerable care is taken to exclude air during the polymerization stages of manufacturing. This inhibitory effect has been shown to be caused by copolymerization of oxygen with monomer, forming an alternating copolymer (81,82). [Pg.165]

The early kinetic models for copolymerization, Mayo s terminal mechanism (41) and Alfrey s penultimate model (42), did not adequately predict the behavior of SAN systems. Copolymerizations in DMF and toluene indicated that both penultimate and antepenultimate effects had to be considered (43,44). The resulting reactivity model is somewhat compHcated, since there are eight reactivity ratios to consider. [Pg.193]

The first quantitative model, which appeared in 1971, also accounted for possible charge-transfer complex formation (45). Deviation from the terminal model for bulk polymerization was shown to be due to antepenultimate effects (46). Mote recent work with numerical computation and C-nmr spectroscopy data on SAN sequence distributions indicates that the penultimate model is the most appropriate for bulk SAN copolymerization (47,48). A kinetic model for azeotropic SAN copolymerization in toluene has been developed that successfully predicts conversion, rate, and average molecular weight for conversions up to 50% (49). [Pg.193]

Copolymerization is effected by suspension or emulsion techniques under such conditions that tetrafluoroethylene, but not ethylene, may homopolymerize. Bulk polymerization is not commercially feasible, because of heat-transfer limitations and explosion hazard of the comonomer mixture. Polymerizations typically take place below 100°C and 5 MPa (50 atm). Initiators include peroxides, redox systems (10), free-radical sources (11), and ionizing radiation (12). [Pg.365]

G-5—G-9 Aromatic Modified Aliphatic Petroleum Resins. Compatibihty with base polymers is an essential aspect of hydrocarbon resins in whatever appHcation they are used. As an example, piperylene—2-methyl-2-butene based resins are substantially inadequate in enhancing the tack of 1,3-butadiene—styrene based random and block copolymers in pressure sensitive adhesive appHcations. The copolymerization of a-methylstyrene with piperylenes effectively enhances the tack properties of styrene—butadiene copolymers and styrene—isoprene copolymers in adhesive appHcations (40,41). Introduction of aromaticity into hydrocarbon resins serves to increase the solubiHty parameter of resins, resulting in improved compatibiHty with base polymers. However, the nature of the aromatic monomer also serves as a handle for molecular weight and softening point control. [Pg.354]

AlkyUithium compounds are primarily used as initiators for polymerizations of styrenes and dienes (52). These initiators are too reactive for alkyl methacrylates and vinylpyridines. / -ButyUithium [109-72-8] is used commercially to initiate anionic homopolymerization and copolymerization of butadiene, isoprene, and styrene with linear and branched stmctures. Because of the high degree of association (hexameric), -butyIUthium-initiated polymerizations are often effected at elevated temperatures (>50° C) to increase the rate of initiation relative to propagation and thus to obtain polymers with narrower molecular weight distributions (53). Hydrocarbon solutions of this initiator are quite stable at room temperature for extended periods of time the rate of decomposition per month is 0.06% at 20°C (39). [Pg.239]

Butadiene—Methacrylic Acid Ionomers. Carboxyl groups can readily be introduced into butadiene elastomers by copolymerization, and the effects of partial neutralization have been reported (63—66). The ionized polymers exhibit some degree of fluidity at elevated temperatures, but are not thermoplastic elastomers, and are very deficient in key elastomer properties such as compression set resistance. [Pg.409]

Polypyrroles. Highly stable, flexible films of polypyrrole ate obtained by electrolytic oxidation of the appropriate pyrrole monomers (46). The films are not affected by air and can be heated to 250°C with Htde effect. It is beheved that the pyrrole units remain intact and that linking is by the a-carbons. Copolymerization of pyrrole with /V-methy1pyrro1e yields compositions of varying electrical conductivity, depending on the monomer ratio. Conductivities as high as 10 /(n-m) have been reported (47) (see Electrically conductive polymers). [Pg.359]


See other pages where Copolymerization Effects is mentioned: [Pg.577]    [Pg.256]    [Pg.149]    [Pg.46]    [Pg.166]    [Pg.3582]    [Pg.4118]    [Pg.865]    [Pg.865]    [Pg.2054]    [Pg.2108]    [Pg.549]    [Pg.577]    [Pg.256]    [Pg.149]    [Pg.46]    [Pg.166]    [Pg.3582]    [Pg.4118]    [Pg.865]    [Pg.865]    [Pg.2054]    [Pg.2108]    [Pg.549]    [Pg.497]    [Pg.317]    [Pg.197]    [Pg.203]    [Pg.278]    [Pg.279]    [Pg.545]    [Pg.354]    [Pg.357]    [Pg.264]    [Pg.267]    [Pg.269]    [Pg.315]    [Pg.364]    [Pg.368]    [Pg.434]    [Pg.480]    [Pg.42]   
See also in sourсe #XX -- [ Pg.97 ]

See also in sourсe #XX -- [ Pg.109 ]




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Acrylonitrile copolymerization solvent effects

Bootstrap effect in copolymerization

Chain copolymerization bootstrap effect

Chain copolymerization pressure effect

Chain copolymerization solvent effect

Chain copolymerization temperature effect

Copolymerization bootstrap effect

Copolymerization effect of solvent

Copolymerization penultimate effect

Copolymerization penultimate unit effects

Copolymerization polar effects

Copolymerization polarity effects

Copolymerization solvent effects

Copolymerization template effects

Effect of Copolymerization on Tg

Ethylene copolymerization solvent effects

Free radical copolymerization pressure effects

Initiator effect, copolymerization

Maleic anhydride copolymerization bootstrap effect

Penultimate group effect copolymerization

Polar effect radical copolymerization

Pressure effects radical copolymerization

Solvent effects on copolymerization

Steric effect copolymerization

Sty rene copolymerization bootstrap effect

Sty rene copolymerization solvent effects

Vinyl acetate copolymerization solvent effects

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