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Chemical cross-links radical polymerization

Entrapment methods have been used almost exclusively to immobilize plant cells (17). They can be classified into three general groups (24,25) a. gel formation by ionic crosslinking of a charged polymer (ionotropic) b. gel formation by cooling of a heated polymer (thermal), and c. gel formation by chemical reaction (cross-linking, radical polymerization). [Pg.69]

Polymerization of methyl methacrylate monomer with cobalt-60 as source of y-rays, Free radical formation is involved in both cross-linking and polymerization reactions This technique is also being applied in the textile finishing field for grafting and cross-linking fibers with chemical agents for durable-press fabrics. [Pg.1406]

Fig. 1 Representative methods of hydrogel formation. (A) Chemically cross-linked hydrogels are prepared from monomers, oligomers, or polymers in the presence of cross-linking agents. The chemical cross-linking proceeds via radical polymerization or polycondensation reaction. (B) Physically cross-linked hydrogels can be formed by ionic interactions, hydrophobic interaction, or hydrogen bonding. Fig. 1 Representative methods of hydrogel formation. (A) Chemically cross-linked hydrogels are prepared from monomers, oligomers, or polymers in the presence of cross-linking agents. The chemical cross-linking proceeds via radical polymerization or polycondensation reaction. (B) Physically cross-linked hydrogels can be formed by ionic interactions, hydrophobic interaction, or hydrogen bonding.
It was registered above 200°C the effective formation of intermolecular chemical cross-links in the PE-MMT nanocomposite, as a result of recombination reactions of the products of radical decomposition of hydroperoxides, caused by deficiency of oxygen in a polymeric matrix due to the lowered oxygen permeability. [Pg.31]

Li et al. synthesized a PMMA-PEG semi-IPN by radical polymerization and cross-linking of PMMA in the presence of linear PEG, which exhibits two independent shape memory effects at two transition temperatures, the of the PEG crystal and the Tg of the semi-IPN [39]. In the IPN, a single Tg appeared due to the miscibility of the amorphous phase of the two polymers. Based on a reversible order-disorder transition of the crystals below and above the of PEG, and the large difference in storage modulus below and above the Tg of the semi-IPN, the polymer has a recovery ratio of 91 and 99%, respectively For the shape-memory behavior at the of PEG crystals, the fixing phase was the PMMA network and the reversible phase was PEG crystals. For the shape memory behavior at the Tg of the semi-IPNs, the fixing phase was the chemical cross-linked point, while the reversible phase was the PMMA-PEG complex phase. [Pg.138]

Responsive NC-gels are based on PNIPAAm and can be prepared by different strategies. The synthesis by free-radical polymerization follows the strategy of chemical cross-linking. [Pg.388]

Spoly(vinylbenzylchloride). -Cross-linked using divinylbenzene. Chloromethylated, cross-linked polystyrene resins were obtained coiranercielly from Bio-Rad Laboratories. Percent chloromethylation js based on the available phenyl groups in the polymer that is minus the percent cross-linking. =D=dioxane E ethanol. Percent of available chloromethyl croups reacted with donor. —Percent reaction x percent chloromethylation. Polymer prepared by free-radical polymerization of 60.00 para-neta chloromethylated sytrene (Dow Chemical). Reaction heated at 50-55°C. [Pg.436]

As an alternative, stable high-coverage nonpolar RPC sorbents phases have been prepared by cross-linking hydrophobic polymers at the silica surface, either via free radical 143 or condensation 101 polymerization chemistry. In this case, the underlying silica becomes partly protected from hydrolytic degradation due to the presence of the hydrophobic polymer film coating that effectively shields the support material. Similar procedures have been employed to chemically modify the surface of other support materials, such as porous zirconia, titania, or alumina, to further impart resistance to degradation when alkaline mobile-phase conditions are employed. Porous polystyrene-divinylbenzene sorbents, be-... [Pg.583]

The primary effect of any ionizing radiation is based on its ability to excite and ionize molecules, and this leads to the formation of free radicals, which fhen initiate reactions such as polymerization and cross-linking or degradation. Accelerated electron beams have energy sufficient to affect the electrons in the atom shell, but not its nucleus, and can therefore only initiate chemical reactions. Typically, the reactions initiated by electron beam are extremely fast and are completed in fractions of a second. [Pg.14]


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See also in sourсe #XX -- [ Pg.219 ]




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Chemical cross-linking

Chemical cross-links

Chemically polymeric

Chemically-cross-linked

Cross-linking polymerization

Cross-linking radical

Cross-polymerized

Polymerization cross

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