Ternary 137 monomer

The modacrylic fibres have similar properties to those of acrylics and are flame resistant..Mostly this fibre is based on a 60/40 or 50/50 copolymer of acrylonitrile with vinylidine chloride (CH = CCy together with small proportion of ternary monomer to improve ionic dyeability or hydrophilicity. The better known modacrylic fibres have a ribbon-shaped or pea-nut shaped cross-section. One problem encountered with modacrylic fibre is loss of lustre at the boil [83, 84]. This fibre is used for apparel, home furnishing, wigs etc. 

Table 5.8 and Fig. 5.1 illustrate the effect of hexafluoropropylene concentration in the monomer mixture on the incorporation of PPVE. The incorporation of PPVE is at a low 1.1 % by weight without the addition of HFP. The extent of incorporation of perfluoropropylvinyl ether increases slowly with the addition of HFP. It accelerates significantly beyond 4% hexafluoropropylene in the ternary monomer mixture up to a point (between 14.7 and 23.3% HFP) and then begins to decrease. The melting point decreases with HFP and begins to increase in this same range. 

In block copolymers [8, 30], long segments of different homopolymers are covalently bonded to each otlier. A large part of syntliesized compounds are di-block copolymers, which consist only of two blocks, one of monomers A and one of monomers B. Tri- and multi-block assemblies of two types of homopolymer segments can be prepared. Systems witli tliree types of blocks are also of interest, since in ternary systems the mechanical properties and tire material functionality may be tuned separately. 

It may be noted here that it is frequently possible to polymerise two monomers together so that residues from both monomers occur together in the same polymer chain. In addition polymerisation this normally occurs in a somewhat random fashion and the product is known as a binary copolymer. It is possible to copolymerise more than two monomers together and in the case of three monomers the product is referred to as a ternary copolymer or terpolymer. The term homopolymer is sometimes used to refer to a polymer made from a single monomer. 

In consequence ethylene-propylene rubbers were introduced with a small amount (3-8%) of a third, diene, monomer which provided a cross-link site for accelerated sulphur vulcanisation. Such ethylene-propylene-diene monomer ternary copolymers are designated as EPDM rubbers. 

MAIs may also be formed free radically when all azo sites are identical and have, therefore, the same reactivity. In this case the reaction with monomer A will be interrupted prior to the complete decomposition of all azo groups. So, Dicke and Heitz [49] partially decomposed poly(azoester)s in the presence of acrylamide. The reaction time was adjusted to a 37% decomposition of the azo groups. Surface active MAIs (M, > 10 ) consisting of hydrophobic poly(azoester) and hydrophilic poly(acrylamide) blocks were obtained (see Scheme 22) These were used for emulsion polymerization of vinyl acetate—in the polymerization they act simultaneously as emulsifiers (surface activity) and initiators (azo groups). Thus, a ternary block copolymer was synthesized fairly elegantly. 

The existence of an azeotropic composition has some practical significance. By conducting a polymerization with the monomer feed ratio equal to the azeotropic composition, a high conversion batch copolymer can be prepared that has no compositional heterogeneity caused by drift in copolymer composition with conversion. Thus, the complex incremental addition protocols that arc otherwise required to achieve this end, are unnecessary. Composition equations and conditions for azeotropic compositions in ternary and quaternary eopolymerizations have also been defined.211,21... 

Terpolymerizations or ternary copolymerizations, as the names suggest, are polymerizations involving three monomers. Most industrial copolymerizations involve three or more monomers. The statistics of terpolymerization were worked out by Alfrey and Goldfinger in 1944.111 If we assume terminal model kinetics, ternary copolymerization involves nine distinct propagation reactions (Scheme 7.9). 

Azeotropic compositions are rare for terpolymerization and Ham 14 has shown that it follows from the simplified eqs. 38-40 that ternary azeotropes should not exist. Nonetheless, a few systems for which a ternary azeotrope exists have now been described (this is perhaps a proof of the limitations of the simplified equations) and equations for predicting whether an azeotropic composition will exist for copolymerizations of three or more monomers have been formulated.20113 This work also shows that a ternary azeotrope can, in principle, exist even in circumstances where there is no azeotropic composition for any of the three possible binary copolymerizations of tire monomers involved. 

The influence of selectivity in the initiation, termination or chain transfer steps on the distribution of monomer units within the copolymer chain is usually neglected. Galbraith et a .u provided the first detailed analysis of these factors. They applied Monte Carlo simulation to examine the influence of the initiation and termination steps on the compositional heterogeneity and molecular weight distribution of binary and ternary copolymers. Spurting et a/.250 extended this... 

Interesting TPEs can be derived from binary and ternary blends of polyfunctional acrylates, ACM, and fluorocarbon rubber (FKM) [53]. During the blend preparation, the liquid multifunctional acrylate monomer used is polymerized and forms the continuous matrix encapsulating the... 

In this work, a comprehensive kinetic model, suitable for simulation of inilticomponent aiulsion polymerization reactors, is presented A well-mixed, isothermal, batch reactor is considered with illustrative purposes. Typical model outputs are PSD, monomer conversion, multivariate distritution of the i lymer particles in terms of numtoer and type of contained active Chains, and pwlymer ccmposition. Model predictions are compared with experimental data for the ternary system acrylonitrile-styrene-methyl methacrylate. 

Model predictions are caipared with experimental data In the case of the ternary system acrylonitrlle-styrene-methyl methacrylate. Ihe experimental runs have been performed with the same recipe, but monomer feed composition. A glass, thermostat ted, well mixed reactor, equipped with an anchor stirrer and four baffles, has been used. The reactor operates under nitrogen atmosphere and a standard degassing procedure is performed Just before each reaction. The same operating conditions have been maintained in all runs tenperature = 50°C, pressure = 1 atm, stirring speed = 500 rpm, initiator (KgSgOg) 0. 395 gr, enulsifier (SLS) r 2.0 gr, deionized water = 600 gr, total amount of monomers = 100 gr. 

We can also illustrate the interesting non-additivity of multiple donor-acceptor interactions involving the same monomer. For this purpose we consider the ternary NO+(C2H4)2 complex in which two ethylene molecules donate to the same... 

The fall of the DP from the peak as the solvent monomer ratio becomes very great (very low monomer concentration) may be at least partly due to the progressive formation of the ternary complexes of the type A1C13,2G which are efficient chain-breakers. 

The ternary complex consisting of the carbenium ion with an anion and a monomer molecule can isomerise with incorporation of the previously complexed monomer molecule into the chain and a shift of the positive charge to the new chain end. This is a unimolecular propagation reaction of zero order with respect to the monomer concentration. It occurs in polymerisations of bulk monomer and in nonpolar solvents, and at relatively high monomer concentrations in polar solvents. 

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