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Copolymer mixture

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]

A multicomponent dynamic RPA for incompressible diblock copolymer mixtures was developed by Akcasu [270]. The details of the approach may be found in the above reference. Here we recall some basic ideas dealing with the calculation of the dynamic structure factor S Q,t) for Rouse chains. [Pg.163]

Schwahn, D. Willner, L. Phase Behavior and Flory-Huggins Interaction Parameter of Binary Polybutadiene Copolymer Mixtures with Different Vinyl Content and Molar Volume. Macromolecules 2002,35, 239-247. [Pg.679]

We now consider the random copolymer model in the presence of solvent— that is, for a copolymer volume fraction p0 < 1. We are not aware of previous work on this model in the literature, but will briefly discuss below the link to models of homopolymer/copolymer mixtures [57]. The excess free energy (86) then depends on two moment densities, rather than just one as in all previous examples. For simplicity, we restrict ourselves to the case of a neutral solvent that does not in itself induce phase separation this corresponds to X = 0, making the excess free energy... [Pg.321]

Melt Viscosity of PVC-Graft Copolymer Mixtures. Table III shows that the presence of 15 phr of a VC/PE (50-50) graft copolymer in a rigid PVC compound lowers its melt viscosity considerably. This effect is more pronounced for the graft copolymers with a low-molecular-weight PVC fraction. [Pg.157]

Table III. Melt Viscosity of PVC-VC/PE Graft Copolymer Mixtures... Table III. Melt Viscosity of PVC-VC/PE Graft Copolymer Mixtures...
Figure 15. Top fractionation of mixtures of PVC-graft copolymers. Bottom fractionation curves for different compositions of PVC-graft copolymer mixtures... Figure 15. Top fractionation of mixtures of PVC-graft copolymers. Bottom fractionation curves for different compositions of PVC-graft copolymer mixtures...
Table 1. Removal of PVAc from a PVAc-PS-PVAc-styrene graft copolymer mixture by the modified precipitation (initial polymer cone. = 2 g/dl)... Table 1. Removal of PVAc from a PVAc-PS-PVAc-styrene graft copolymer mixture by the modified precipitation (initial polymer cone. = 2 g/dl)...
PP possesses good water vapor barrier and fat resistance properties. Normal PP films have limited food packaging applications (e.g. packaging of bread) because of their low cold temperature resistance. Copolymer mixtures with ethylene are used to improve cold resistance and heat sealability as well as material strength and, above all, seal strength. [Pg.26]

The breakthrough to bulk plastic was made possible by the development of ABS polymers. This copolymer mixture leads to a combination of technologically important properties that have allowed its use for many diverse applications. [Pg.29]

Appendix A Multicomponent Random Phase Approximation for Homopolymer and Copolymer Mixtures... [Pg.126]

Consider a polymer system consisting of n components. These could be homopolymer mixtures or homopolymer and copolymer mixtures. In order to simplify the calculations, we consider that at least one of the components (that we call matrix component) is a homopolymer. The formalism presented here is a straightforward extension of the two-component case in an n-vector and nxn matrix notation [13] ... [Pg.126]

This generalization of de Gennes formula to multicomponent homopolymer and copolymer blends can describe a wide variety of situations. After a slight generalization (described in Appendix B) it can also, describe the case of pure copolymer mixtures whereby a copolymer has to be shared between M and R. Using Appendix A, one could obtain this limit (pure copolymer mixtures) by... [Pg.127]

Table III shows the increase of molecular weight of BCMO polymerization with conversion, although the polymer tends to precipitate. The monomer reactivity ratios of DOL-BCMO copolymerization were previously determined as rx (DOL) = 0.65 0.05, r2 (BCMO) = 1.5 0.1 at 0°C. by BF3 Et20 (8). Table IV shows a preparation of block copolymer of DOL, St, and BCMO. In the first step we polymerized DOL and St in the second step we added BCMO to this living system. The copolymer obtained showed an increase of molecular weight, and considerable BCMO was incorporated in the copolymer still remaining soluble in ethylene dichloride. The solubility behavior together with the increase of molecular weight with addition of BCMO shows that this polymer consists of block sequences of DOL-St and (St)-DOL-BCMO. This we call block and random copolymer of DOL-St—BCMO. We can deny the presence of BCMO, St, or DOL homopolymers in this system, but some chain-breaking reactions are unavoidable, leading to copolymer mixtures. Thus, the principle of formation of block copolymers by cationic system is partly substantiated. Table III shows the increase of molecular weight of BCMO polymerization with conversion, although the polymer tends to precipitate. The monomer reactivity ratios of DOL-BCMO copolymerization were previously determined as rx (DOL) = 0.65 0.05, r2 (BCMO) = 1.5 0.1 at 0°C. by BF3 Et20 (8). Table IV shows a preparation of block copolymer of DOL, St, and BCMO. In the first step we polymerized DOL and St in the second step we added BCMO to this living system. The copolymer obtained showed an increase of molecular weight, and considerable BCMO was incorporated in the copolymer still remaining soluble in ethylene dichloride. The solubility behavior together with the increase of molecular weight with addition of BCMO shows that this polymer consists of block sequences of DOL-St and (St)-DOL-BCMO. This we call block and random copolymer of DOL-St—BCMO. We can deny the presence of BCMO, St, or DOL homopolymers in this system, but some chain-breaking reactions are unavoidable, leading to copolymer mixtures. Thus, the principle of formation of block copolymers by cationic system is partly substantiated.
CSTRl, copolymerization reactor continuously supplying the ethylene-comonomer-copolymer mixture... [Pg.176]

The use of polysilanes as photoinitiators of radical polymerization was one of the hrst means whereby they were incorporated within block copolymer structures [38 0], albeit in an uncontrolled fashion. However the resulting block copolymer structures were poorly defined and interest in them principally lay in their application as compatibilisers for polystyrene (PS) and polymethylphenylsilane blends PMPS. The earliest synthetic strategies for relatively well-defined copolymers based on polysilanes exploited the condensation of the chain ends of polysilanes prepared by Wurtz-type syntheses with those of a second prepolymer that was to constitute the other component block. Typically, a mixture of AB and ABA block copolymers in which the A block was polystyrene (PS) and the B block was polymethylphenylsilane (PMPS) was prepared by reaction of anionically active chains ends of polystyrene (e.g. polystyryl lithium) with Si-X (X=Br, Cl) chain ends of a,co-dihalo-polymethylphenylsilane an example of which is shown in Fig. 2 [43,44,45]. Similar strategies were subsequently used to prepare an AB/ABA copolymer mixture in which the A block was poly(methyl methacrylate) (PMMA) [46] and also a multi- block copolymer of PMPS and polyisoprene (PI) [47]. [Pg.252]

Knoll [1] anionically prepared styrene-butadiene block copolymer mixtures using sec-butyllithium followed by hydrogenation, and the material was then used as transparent films. [Pg.464]

Fig. 58 Generation of mesoporous structures from supramolecular block copolymers. TEM-micrograph after extraction of the zinc-dodecylbenzenesolphonate from a PS-P4VP diblock copolymer mixture. Reprinted with permission from [212]... Fig. 58 Generation of mesoporous structures from supramolecular block copolymers. TEM-micrograph after extraction of the zinc-dodecylbenzenesolphonate from a PS-P4VP diblock copolymer mixture. Reprinted with permission from [212]...
Of the reported materials, the only commercially available resists are one of the MMA-MAA/MMA-MACl compositions and a t-butyl methacrylate copolymer material (13). In this work, we have chosen to examine the copolymer mixture, which crosslinks at a temperature of 160°C compared to 250 C for the single copolymer. We have carried out experiments to optimize its use for direct write electron beam lithography. [Pg.87]

Other methods of reducing the crosslink density have also led to sensitivity improvements, of which the most promising is the uneven copolymer mixtures with a potential 60-70% reduction in operating dose. However, the solutions must be aged after mixing in order to obtain reproducible performance. This technique also requires work on a developer system. Flood exposure yields a 50% improvement in sensitivity but creates additional processing difficulties due to double exposure effects. [Pg.96]

D. P. Serrano, J. Aguado, J. M. Escola, J. M. Rodriguez, L. Morselli, and R. Orsi, Thermal and catalytic cracking of a LDPE-EVA copolymer mixture, J. Anal. Appl. Pyrolysis 68-69, 481 (2003). [Pg.105]

Multicomponent Star Block Copolymer on Gradient HPLC-SEC System. The 16-component star block copolymer mixture was injected into a gradient HPLC (i-octane-THF) on a silica column (60-A pore size) to get a good separation by chemical composition. These fractions were transferred automatically by an electrically driven injection valve into the second dimension (SEC in THE cf. Figure 2). [Pg.231]

M. Muller and M. Schick (1996) Bulk and interfacial thermodynamics of a symmetric, ternary homopolymer-copolymer mixture A Monte Carlo study. J. Chem. Phys. 105, pp. 8885-8901... [Pg.125]

A very controlled manner of organizing nanoparticle/copolymer mixtures was achieved by Lin et al. [257], by applying a nonconjugated block copoly-... [Pg.56]

Panayiotou, C. G. 1987. Thermodynamics of random copolymer mixtures. Makromol. [Pg.532]


See other pages where Copolymer mixture is mentioned: [Pg.130]    [Pg.638]    [Pg.11]    [Pg.62]    [Pg.58]    [Pg.59]    [Pg.88]    [Pg.125]    [Pg.177]    [Pg.177]    [Pg.338]    [Pg.99]    [Pg.294]    [Pg.59]    [Pg.3280]    [Pg.231]    [Pg.444]    [Pg.100]    [Pg.82]    [Pg.99]    [Pg.388]    [Pg.39]   
See also in sourсe #XX -- [ Pg.127 ]




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