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Addition polymerization copolymers

Haward et al.t have reported some research in which a copolymer of styrene and hydroxyethylmethacrylate was cross-linked by hexamethylene diisocyanate. Draw the structural formula for a portion of this cross-linked polymer and indicate what part of the molecule is the result of a condensation reaction and what part results from addition polymerization. These authors indicate that the crosslinking reaction is carried out in sufficiently dilute solutions of copolymer that the crosslinking is primarily intramolecular rather than intermolecular. Explain the distinction between these two terms and why concentration affects the relative amounts of each. [Pg.339]

As recently as 1986 almost all addition polymers were excluded from the ranks of engineering plastics. However, progress since then has been made in the development of addition polymeric resins such as polymethylpentene and polycyclopentadiene and its copolymers (see Cyclopentadiene AND DICYCLOPENTAD IENE). [Pg.276]

A copolymer, on the other hand, results from two different monomers hy addition polymerization. For example, a thermoplastic polymer with better properties than an ethylene homopolymer comes from copolymerizing ethylene and propylene ... [Pg.302]

The literature reports various (multidimensional) chromatographic approaches involving SEC and LC operating on dissolved polymer/additive mixtures. Floyd [985] has used microbore (1 mm i.d.) SEC-RPLC for the quantitative analysis of Tinuvin P in a cellulose acetate solution in THF, after separation of the polymeric and additive fractions total analysis time about 30 min. Relative accuracy and precision of 3 % and 1.5% were quoted. SEC-RPLC was also used to determine the styrene level in polystyrene crystals [986]. Additives in copolymers have been separated in a SEC/C system [987]. Chlorohydrin mixtures may be analysed by RPLC, but not in the presence of polymer. Thus, SEC... [Pg.557]

Copolymers are formed when two different monomers are mixed and then polymerized. It is possible to produce a copolymer by addition polymerization. An example is SBR, the most important rubber produced in the United States. It is a copolymer of styrene and butadiene in a 1 3 ratio. [Pg.400]

Cyclopolymerization of Nonconjugated Dienes. Cyclopolymerization is an addition polymerization that leads to introduction of cyclic structures into the main chain of the polymer. Nonconjugated dienes are the most deeply studied monomers for cyclopolymerization and for cyclocopolymerizations with alkene monomers 66 In general, (substituted and unsubstituted) dienes with double bonds that are linked by less than two or more than four atoms cannot undergo efficient cyclization and result in crosslinked materials.12 In fact, efficient cyclopolymerization processes have been described, for instance, for a,oo-dienes like 1,5-hexadiene, 2-methyl-l,5-hexadiene, 1,6-heptadiene, and 1,7-octadiene,67 73 which lead to formation of homopolymers and copolymers containing methylene-1,3-cycloalkane units. [Pg.26]

Copolymers. Mixtures of two or more different bifunctional monomers can undergo additional polymerization to form copolymers. Why copolymerize Well, polymers have different properties that depend on their composition, molecular weight, branching, crystallinity, etc. Many copolymers have been developed to combine the best features of each monomer. For example, polystyrene is low cost and clear, but it is also brittle with no toughness. It needs internal plasticization. By copolymerizing styrene with a small amount of acrylonitrile or butadiene, the impact and toughness properties are dramatically improved. [Pg.325]

For the synthesis of block copolymers chain addition polymerization (ionic or radical) as well as condensation polymerization and stepwise addition polymerization can be used. [Pg.250]

In this paper a generalized approach is presented to the derivation of H-H-S equations for multispecies polymers created by addition polymerization across single double bonds in the monomers. The special cases of copolymers and terpolymers are derived. This development is combined with experimental results to evaluate the numerical parameters in the equations for poly(styrene-acrylonitrile ) (SAN) in three separate solvents and for poly(styrene-maleic anhydride-methyl methacrylate) (S/HA/MM) in a single solvent. The three solvents in the case of SAN are dimethyl formamide (DMF), tetrahydrofuran (THF), and methyl ethyl ketone (MEK) and the solvent for S/HA/HH is HER. [Pg.264]

We attempt here to develop a mathematical expression for the dependence of the dilute solution intrinsic viscosity of multispecies polymers on both molecular weight and polymer composition with some broad degree of generality and to particularize the result for the specific cases of copolymers and terpolymers such as SAN and S/MA/MM. The details of the derivation are specific to polymers resulting from addition polymerization across a single double bond in each monomer unit. In principle the approach may be expanded to other schemes of polymerization so long as... [Pg.264]

Table 3.7 Typical Monomer Reactivity Ratios in the Addition Polymerization of Copolymers... Table 3.7 Typical Monomer Reactivity Ratios in the Addition Polymerization of Copolymers...
The newly formed R may also add to another alkene molecule to give a trimer. The process whereby simple molecules, or monomers, are merged can continue, eventually giving high-molecular-weight molecules called polymers. This reaction of alkenes is called chain-growth (addition) polymerization. The repeating unit in the polymer is called the mer. If a mixture of at least two different monomers polymerizes, there is obtained a copolymer. [Pg.104]

Poly(cycloalkene)s obtained from the vinyl addition polymerization method exhibit extremely high melting points. The high melting points make the polymers unprocessable. For this reason, comonomers, such as ethene or propene are introduced to lower the melting points. Copolymers of this type are addressed as COCs. [Pg.44]

Radicals are employed widely in the polymer industry, where their chain-propagaling behavior transforms vinyl monomers into polymers and copolymers. The mechanism of addition polymerization involves all three types of reactions discussed above, i.e., initiation, propagation by addition to carbon-carhon double bonds, and termination. [Pg.840]

Procedure 3 Addition of MPP to Polymerizing DMP. Procedure 1 was followed with only the DMP initially present. After two hours, the MPP was added, causing a prolonged decrease in solution viscosity oxidation was continued for three hours after MPP addition. The copolymer was obtained in 92% yield, with an intrinsic viscosity of 0.58 dl/g. [Pg.251]

How does living polymerization differ from ordinary addition polymerization Show how the former can be used to synthesize styrene-butadiene-styrene block copolymers. [Pg.85]

The composition of llie copolymer formed from n monomers in addition polymerization can be expressed in terms of the monomer feed composition and n n — 1) binary reactivity ratios. Thus, for terpolymerization [16],... [Pg.257]


See other pages where Addition polymerization copolymers is mentioned: [Pg.321]    [Pg.32]    [Pg.4]    [Pg.111]    [Pg.80]    [Pg.108]    [Pg.88]    [Pg.221]    [Pg.84]    [Pg.7]    [Pg.403]    [Pg.184]    [Pg.107]    [Pg.118]    [Pg.133]    [Pg.7]    [Pg.384]    [Pg.282]    [Pg.728]    [Pg.14]    [Pg.50]    [Pg.55]    [Pg.267]    [Pg.605]    [Pg.606]    [Pg.168]   
See also in sourсe #XX -- [ Pg.325 ]




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Addition polymerization

Additional polymerization

Additives polymerization

Copolymer addition

Polymeric additives

Polymerization copolymers

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