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Polysiloxane structures

Alkoxysilanes undergo hydrolysis, condensation (catalysts for alkoxysilane hydrolysis are usually catalysts for condensation), and a bond formation stage under base as well as under acid catalyzed mechanisms. In addition to this reaction of silanols with hydroxyls of the fiber surface, the formation of polysiloxane structures also can take place. [Pg.798]

Figure 3.23 Graftable polysiloxane structures. After Gray and... Figure 3.23 Graftable polysiloxane structures. After Gray and...
Polymerization was carried out in NaOH aqueous solution. Table 4 summarizes the reaction conditions and polymer yields. The first step of the polymerization was hydrolysis and oligomerization of the silylethers at low temperatures from 90°C to 150 °C. In order to increase the polymer yield and the softening point of the polymers, the second step was carried out at higher temperatures under reduced pressure, removing alcohol and water, 1H-NMR, 13CNMR and IR spectroscopy of each polymer show that these polymers have the polysiloxane structure substituted with a phenol group. [Pg.153]

Carr et al. [252] studied LB films made from preformed polymers based on the polysiloxane structure. Such materials have attracted attention as liquid crystal side chain polymers as they remain in a mesophase at low temperatures but, just for this reason, they seem unlikely materials to form stable LB films. [Pg.99]

Table 4.1 Some Polysiloxane Structural Changes and Expected Changes in Properties... Table 4.1 Some Polysiloxane Structural Changes and Expected Changes in Properties...
Cyclic siloxanes form more rapidly from DMS at higher temperatures because of increased rates of thermal rearrangement of the polysiloxane structure (1, 2,16, 26, 29). [Pg.112]

It is necessary that the silicol condense at a rate comparable to that for orthosilicic acid, since otherwise the latter will condense only with itself and will precipitate as silica before it can be included within the siloxane network. It also is found by experiment that only a rather small proportion of SiX4 may be included in the mixture of intermediates if the precipitation of silica is to be avoided. However, the mere fact that appreciable amounts of silica can be combined chemically within the polysiloxane structure is strong evidence in support of the theory of intermolecular condensation as given here, and at the same time it illustrates the close chemical similarity between silica and the organosiloxanes. [Pg.55]

The use of organometallic polymers in the bilevel RIE-PCM scheme was first reported by Shaw et al. (185). They used polysiloxane (structure 3.16) as a negative-working electron beam imaging layer. The etch rate ratio... [Pg.192]

Figure 4. Schematic representation of a cross-linked polysiloxane structure formed by copolycondensation of tetraalkoxysilane, propyltrialkoxysilane and 3-(tris-hydroxy-silyl)propyl sulfonic acid. Note the embedding of the functionalized. siloxanes into the matrix in contrast with simple attachment to the surface of a preformed solid. Figure 4. Schematic representation of a cross-linked polysiloxane structure formed by copolycondensation of tetraalkoxysilane, propyltrialkoxysilane and 3-(tris-hydroxy-silyl)propyl sulfonic acid. Note the embedding of the functionalized. siloxanes into the matrix in contrast with simple attachment to the surface of a preformed solid.
ACRONYM PDBuS CLASS Polysiloxanes STRUCTURE [-(C4H9)2SiO ]... [Pg.394]

Table 1.2. NOTATIONS FOR VARIOUS POLYSILOXANE STRUCTURAL UNITS ... [Pg.4]

Table 5.1. SOME POLYSILOXANE STRUCTURAL CHANGES AND EXPECTED CHANGES IN PROPERTIES ... Table 5.1. SOME POLYSILOXANE STRUCTURAL CHANGES AND EXPECTED CHANGES IN PROPERTIES ...
To obtain homeotropic alignment by surface active agent treatment of the substrate surface, silicon compoimds are usually used as the surface active agent. Silicon compounds, such as alkoxysilanes or chlorosilanes, react with the substrate surface following Scheme 3.7.1 and pol5mierize to form polysiloxane structures near the surface. [Pg.90]

Unusual polysiloxane structures that were covered at the symposium are stiffened chains (Van Dyke, Zhang, Lauter), cyclics (Semiyen, Dagger), ladders and cages (41) (Crivello, Lichtenham, Feher, Rebrov, Carpenter, Rahimian, Haddad),hyperbranched structures (Moller, Herzig, Muzafarov, Vasilenko), dendrimers (42,43) (Dvornic, Owen, Vasilenko, Sheiko, Rebrov), and sheets and tubes (Kenney, Katsoulis) (26),... [Pg.3]

Silicones are synthetic polymeric materials which may be formulated to have a very wide range of properties. All have a basic polysiloxane structure, giving them a combination of organic and inorganic chemical properties. These properties have made them of interest for adhesive and sealing applications. Their main features are ... [Pg.4]

The effects of polysiloxane structures on transport properties are reviewed in detail (Stem et al., 1987). In particular, polydimethylsiloxane (PDMS) is the most important siloxane polymer (Rochow, 1987). Particularly, it is a useful membrane material for gas and vapor separation. PDMS is known as the most permeable mbbery polymer. Due to... [Pg.646]


See other pages where Polysiloxane structures is mentioned: [Pg.678]    [Pg.700]    [Pg.257]    [Pg.133]    [Pg.66]    [Pg.71]    [Pg.3986]    [Pg.139]    [Pg.3985]    [Pg.544]    [Pg.450]    [Pg.678]    [Pg.700]    [Pg.606]    [Pg.374]    [Pg.378]    [Pg.364]    [Pg.180]    [Pg.91]   
See also in sourсe #XX -- [ Pg.55 ]




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