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Polydimethylsiloxane , grafted

Nagase Y, Naruse A, and Matsui K. Chemical modification of polysulphone. 2. Gas and liquid permeability of polysulpho-ne/polydimethylsiloxane graft copolymer membranes cf Polymer. 1990 31(1) 121-125. [Pg.136]

M. Dabagh, M.J. Abdekhodaie, M.T. Khorasani, Effects of polydimethylsiloxane grafting on the calcification, physical properties, and biocompatibility of polyurethane in a heart valve, J. Appl. Polym. Sci. 98 (2005) 758-766. [Pg.326]

Hu, A. Cui, Y. Wei, X. Lu, Z. Ngai, T., Hydrogen-Bonding-Induced Complex-ation of Polydimethylsiloxane-graft-poly(ethylene oxide) and Poly(acrylic acid)-h/oc/c-Polyacrylonitrile Micelles in Water. Langmuir 2010,26, 14502-14508. [Pg.214]

Surface active agents are important components of foam formulations. They decrease the surface tension of the system and facilitate the dispersion of water in the hydrophobic resin. In addition they can aid nucleation, stabilise the foam and control cell structure. A wide range of such agents, both ionic and non-ionic, has been used at various times but the success of the one-shot process has been due in no small measure to the development of the water-soluble polyether siloxanes. These are either block or graft copolymers of a polydimethylsiloxane with a polyalkylene oxide (the latter usually an ethylene oxide-propylene oxide copolymer). Since these materials are susceptible to hydrolysis they should be used within a few days of mixing with water. [Pg.797]

ESCA analysis showed a similar trend of incomplete surface coverage for the IK systems. Also, no domains were visible in any of the IK styrenic graft systems by TEM. There is an expected trend with respect to solubility parameter, p(t-butyl styrene) (6 s 8.1) has a solubility parameter much closer to that of polydimethylsiloxane (S a 7.3) than does p(p-methyl styrene) which is closer than p(styrene) (S s 9.1). [Pg.96]

In this paper we describe methods in which polystyrene (PS) and polydimethylsiloxane (PDMS) have been successfully grafted to silica particles, avoiding the dry stage. [Pg.282]

Fig. 10 Plots of Le/f-cw vs. dimensionless graft density a (1) PS brushes prepared by adsorption of PS-polydimethylsiloxane block copolymers (Mw,ps = 60000) and 0 (Mw,ps = 169000) [21,22]. (2) PEO brushes prepared by adsorption of PEO-PS block copolymers A (Mw.peo = 30800) and V (Mw.peo = 19600) [201]. (3) PMMA brushes prepared by surface-initiated ATRP (M = 31 300 267400). Data reprocessed from [116,117]... Fig. 10 Plots of Le/f-cw vs. dimensionless graft density a (1) PS brushes prepared by adsorption of PS-polydimethylsiloxane block copolymers (Mw,ps = 60000) and 0 (Mw,ps = 169000) [21,22]. (2) PEO brushes prepared by adsorption of PEO-PS block copolymers A (Mw.peo = 30800) and V (Mw.peo = 19600) [201]. (3) PMMA brushes prepared by surface-initiated ATRP (M = 31 300 267400). Data reprocessed from [116,117]...
Abstract We review various methods for the photochemical grafting of organic polymers to various substrates including, organic films, membranes, planar gold, silicon wafers, glass, silica gel, silica nanoparticles, and polydimethylsiloxane micro-channels. An emphasis is placed on photoinitiated synthesis of polymer brushes from planar gold and silicon. [Pg.47]

Recently Allbritton and Li coated polydimethylsiloxane (PDMS) microfluidic channels with BP [36]. Upon irradiation in the presence of a monomer solution, they were able to graft poly(acrylic acid) and poly(ethylene glycol) monomethoxyl acrylate to the interior walls of the channels. This is a significant achievement since the device did not require disassembly in order to modify the channel walls. The electrophoretic separation of the modified channels was different from the native channels. This technique holds particular promise for the microfluidic separations commimity. [Pg.53]

Most dispersion polymerizations in C02, including the monomers methyl methacrylate, styrene, and vinyl acetate, have been summarized elsewhere (Canelas and DeSimone, 1997b Kendall et al., 1999) and will not be covered in this chapter. In a dispersion polymerization, the insoluble polymer is sterically stabilized as colloidal polymer particles by the surfactant that is adsorbed or chemically grafted to the particles. Effective surfactants in the dispersion polymerizations include C02-soluble homopolymers, block and random copolymers, and reactive macromonomers. Polymeric surfactants for C02 have been designed by combining C02-soluble (C02-philic) polymers, such as polydimethylsiloxane (PDMS) or PFOA, with C02-insoluble (C02-phobic) polymers, such as hydrophilic or lipophilic polymers (Betts et al., 1996, 1998 Guan and DeSimone, 1994). Several advances in C02-based dispersion polymerizations will be reviewed in the following section. [Pg.154]

The same authors attempted copolymerization of these silicone — type macromonomers with different monomers (e.g. styrene) with the aim of synthesizing graft copolymers. a,ra-Diunsaturated polydimethylsiloxanes were also synthesized by the same method starting from i,m-dichlorodimethylsiloxane oligomers. [Pg.4]

It should be underlined that it was possible to obtain slip at low stress values, by considering the flow of a polydimethylsiloxane (PDMS) through a silica die with walls grafted by a fluorinated monolayer [11]. It can also be found in the experimental study published in 1993 by Migler et al. [12], which moreover validates the model prediction in term of extrapolation length, for sufficiently high slip velocities. [Pg.358]


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