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Polymerization, poly networks

We have shown that similar networks formed from bis(chloromethyl)biphenyl (BCMBP) exhibit surface areas as high as 1,904 m g [31]. Webster and coworkers have prepared HCPs by treating 4,4 -dilithiobiphenyl (as well as other multi-lithiated aromatic compounds) with dimethylcarbonate to generate polymeric carbinol networks with surface areas of 400-1,000 m g [24]. More recently, poly silane element-organic frameworks was synthesized via a lithiation route to yield microporous networks with BET surface areas in the range 780-1,046 m g" [40]. [Pg.14]

Kalakkunnath, S., Kalika, D. S., Lin, H. Q. Freeman, B. D. (2006) Viscoelastic characteristics of LTV polymerized poly(ethylene glycol) diacrylate networks with... [Pg.86]

Black, insoluble poly(phenylenes) with the monomeric unit - 5114- can be produced from benzene with AICI3/CUCI as catalyst. The polymer is branched, but not cross-linked to a network. The degree of polymerization, measured with the soluble sulfonate derivative, is 100. Stepwise-polymerized poly(l,4-phenylene) is not strongly colored. Consequently, the strong discoloration of poly(phenylenes) produced by polymerizing benzene must result from impurities or from bonding irregularities. [Pg.896]

Kalakkunnath, S., Kalika, D. S., Lin, H., and Freeman, B. D. (2(X)5). Segmental relaxation characteristics of crosslinked poly(ethylene oxide) copolymer networks. Macromolecules 38, 9679. Kalakkurmath, S., Kalika, D. S., Lin, H., and Freeman, B. D. (2(X)6). Viscoelastic characteristics of U.V. polymerized poly(ethylene glycol) diacrylate networks with varying extents of ciosslinking. [Pg.951]

A semi-interpenetrated network was obtained by bulk polymerization of 2-hydroxye-thyl methacrylate incorporated in DMF treated PET films by solvent-exchange technique, followed by treatment of films in e-lectrical discharges. Heparinization was accomplished by reacting glutaraldehyde with heparin and poly(2-hydroxyethyl methacrylate) present on the surface of modified polyester films. The immobilization of heparin was indirectly evidenced by chromatographying the silylated hydrolyza-tes of heparinized PET films and heparin, respectively. In vitro experiments demonstrated the enhanced thromboresistance of heparinized films. [Pg.229]

The ubiquitous hydrosilation reaction, popular especially in silicone manufacturing,132 has been utilized by Houser and Keller for the synthesis of the networked polymers (104) (Fig. 64) from the reaction of the l,7-bis(vinyltetramethyldisiloxyl)-w-carborane monomer with the polymeric crosslinker, poly(methylhydrosiloxane).133 The reactions were catalyzed by the Speier s catalyst, H2PtCl6. Three samples were... [Pg.64]

Figure 64 Hydrosilation reactions between l,7-bis(vinyltetramethyldisiloxyl)-m-carborane monomer and the polymeric cross-linker, poly(methylhydrosiloxane), producing hard, colorless networked plastics. (Adapted from ref. 133.)... Figure 64 Hydrosilation reactions between l,7-bis(vinyltetramethyldisiloxyl)-m-carborane monomer and the polymeric cross-linker, poly(methylhydrosiloxane), producing hard, colorless networked plastics. (Adapted from ref. 133.)...
This process involves the suspension of the biocatalyst in a monomer solution which is polymerized, and the enzymes are entrapped within the polymer lattice during the crosslinking process. This method differs from the covalent binding that the enzyme itself does not bind to the gel matrix. Due to the size of the biomolecule it will not diffuse out of the polymer network but small substrate or product molecules can transfer across or within it to ensure the continuous transformation. For sensing purposes, the polymer matrix can be formed directly on the surface of the fiber, or polymerized onto a transparent support (for instance, glass) that is then coupled to the fiber. The most popular matrices include polyacrylamide (Figure 5), silicone rubber, poly(vinyl alcohol), starch and polyurethane. [Pg.339]

Polymeric pseudocrown ether networks have been generated in situ by the photopolymerization of poly(ethylene glycol) diacrylate transition metal complexes <00CM633>, and the effect of metal ion templation was evaluated. The 1,6,13,18-tetraoxa[6.6]paracyclophane-3,15-diyne (termed pyxophanes) was prepared from hydroquinone and l,4-dichlorobut-2-yne it forms size-selective 7i-complexes with alkali metal cations <00CC2377>. Dibenzo[ ]crown-m have been used in numerous elegant studies in which they were the needles that were threaded by diverse reagents the resultant... [Pg.379]


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See also in sourсe #XX -- [ Pg.183 , Pg.184 , Pg.185 , Pg.186 ]




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