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Polymers network connectivity

In 1988 Heinze and Burton reported a facile synthesis of various a,p,P-trifluorostyrenes.15 These trifluorostyrene compounds were reported to be unstable to cyclodimerization at room temperature when stored neat, especially the compounds that were /lura-substituted with electron-donating substituents. They described the preparation of one compound, l,4-bis(trifluorovinyl)benzene with the observation that the material gelled when allowed to stand neat overnight. They offered the explanation that the gel was a polymer network connected with flnorinated cyclobutanes. Burton later went on to utilize this dimerization reaction for the cross-linking of polyimide thermoplastics.16... [Pg.42]

As it is known [24], solid component fiaction enhancement (namely sueh eomponent of amorphous phase a clusters are as regards devitrificated loosely paeked matrix) results to elastic constant growth. This enhancement can be described quantitatively within the frameworks of percolation theory (see the Eq. (3.7)), but in Ref. [21] the more simple variant was chosen, namely, the polymers network connectivity model [25]. Then the elasticity modulus E value is determined as follows [25] ... [Pg.45]

In this approach, connectivity indices were used as the principle descriptor of the topology of the repeat unit of a polymer. The connectivity indices of various polymers were first correlated directly with the experimental data for six different physical properties. The six properties were Van der Waals volume (Vw), molar volume (V), heat capacity (Cp), solubility parameter (5), glass transition temperature Tfj, and cohesive energies ( coh) for the 45 different polymers. Available data were used to establish the dependence of these properties on the topological indices. All the experimental data for these properties were trained simultaneously in the proposed neural network model in order to develop an overall cause-effect relationship for all six properties. [Pg.27]

Diffusion is not straightforward inside the resin phase, and this is due to the restrictive influences of the polymer network and because of the charge distribution connected with the fixed ions of the functional groups. The resin phase is consequently related to a porous solid. The effectual diffusivities of metal ions in the resin phase may differ but are largely less than those in the aqueous phase external to the resin phase. If Fick s law is applied to diffusion in a resin bead of radius, r, it may be represented as... [Pg.503]

Silicone co-polymer networks and IPNs have recently been reviewed.321 The development of IPNs is briefly described, and the definitions of the main (non-exclusive) classes of the IPNs are cited. Examples of latex IPNs, simultaneous and sequential IPNs, semi-IPNs, and thermoplastic IPNs are provided. The use of silicone-silicone IPNs in studies of model silicone networks is also illustrated. Networks in which siloxane and non-siloxane components are connected via chemical bonds are considered co-polymer networks, although some other names have been applied to such networks. Today, some of the examples in this category should, perhaps, be discussed as organic-inorganic hybrids, or nanocomposites. Silicone IPNs are discussed in almost all of the major references dealing with IPNs.322-324 Silicone IPNs are also briefly discussed in some other, previously cited, reviews.291,306... [Pg.670]

Here D is cooperative diffusion coefficient of the gel. Such a relationship applies to the random or diffusive motions of molecules in a fluid for example, ink molecules in water. It is interesting that the same relation holds for a polymer network even though all the polymers are connected into a single network. [Pg.281]

Fig. la, h. Chemical structure of poly N-isopropylacrylamide (a) and of trisodium salt of copper chlorophyllin molecule (b). The chlorophyllin molecule has a double bond which can be covalently connected to the polymer networks... [Pg.205]

Percolation is widely observed in chemical systems. It is a process that can describe how small, branched molecules react to form polymers, ultimately leading to an extensive network connected by chemical bonds. Other applications of percolation theory include conductivity, diffusivity, and the critical behavior of sols and gels. In biological systems, the role of the connectivity of different elements is of great importance. Examples include self-assembly of tobacco mosaic virus, actin filaments, and flagella, lymphocyte patch and cap formation, precipitation and agglutination phenomena, and immune system function. [Pg.236]

Therefore, the principal difficulty connected with the application of Eq. (12) is due to the incompleteness of the Gauss invariant. So, the use of the Gauss invariant for adequate classification of topologically different states in many-chain systems is very problematic. Nevertheless, that approach was used repeatedly for consideration of such physically important question as the high-elasticity of polymer networks with topological constraints [15]. Unfortunately,... [Pg.8]

An interpenetrating polymer network (IPN) consisting of an epoxy and an elastomer has been developed by Isayama.29 This is a two-component adhesive-sealant where the components are simultaneously polymerized. It consists of the MS polymer, developed in Japan by Kanegafuchi and commonly used in sealant formulations, with the homopolymerization of DGEBA using a phenol catalyst and a small amount of silane as a graft site to connect the MS polymer and epoxy homopolymer networks. [Pg.135]

Aryl tellurium halides, the postulated intermediates, are polymeric substances in which the tellurium atoms are connected by halogen bridges. The polymer network facilitates the migration of aryl groups required by this reaction10. [Pg.334]


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