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Polymeric silicones, applications

Polymeric silicones are extensively used in applications which require thermal stability and long-lasting retention of critical properties. They can be produced in various degrees of hardness and resiliency by combining prepolymer fluids, which contain reactive functional groups, in such ways as to form giant polymer networks with those desired properties. [Pg.169]

This indicates that surface structures can create localized force fields which can trap particles. An interesting application of this concept can be found in the recent work of Sacanna et al. [284]. They created, by clever colloid synthesis, 5 pm (diameter) polymerized silicon oil droplets with a well-defined spherical cavity. To these lock particles they added appropriately sized spherical key particles (silica, poly(methyl methacrylate) or polystyrene coUoids) that can fit into the cavity. Nanometer sized non-adsorbing polymers were added to provide a depletion interaction. The depletion interaction, being proportional to the overlap volume of the depletion zones, attains a maximum when the key particle fits precisely into the spherical cavity of a lock particle, see Fig. 1.31. The depletion-driven self-assembly of lock and key particles is demonstrated in Fig. 1.32. This time series (from left to right) illustrates the site-specificity of the attraction. [Pg.46]

The polymeric/ soft materials chapter represents the largest expansion for the 2nd edition. This chapter describes all polymeric classes including dendritic polymers, as well as important additives such as plasticizers and flame-retardants, and emerging applications such as molecular magnets and self-repairing polymers. This edition now features click chemistry polymerization, silicones, conductive polymers and biomaterials apphcations such as biodegradable polymers, biomedical devices, dmg delivery, and contact lenses. [Pg.749]

Substituted aroyl- and heteroaroyltrimethylsilanes (acylsilanes) are prepared by the coupling of an aroyl chloride with (Me3Si)2 without decarbonylation, and this chemistry is treated in Section 1.2[629], Under certain conditions, aroyl chlorides react with disilanes after decarbonylation. Thus the reaction of aroyl chlorides with disilane via decarbonylation is a good preparative method for aromatic silicon compounds. As an interesting application, trimel-litic anhydride chloride (764) reacts with dichlorotetramethyidisilane to afford 4-chlorodimethylsilylphthalic anhydride (765), which is converted into 766 and used for polymerization[630]. When the reaction is carried out in a non-polar solvent, biphthalic anhydride (767) is formed[631]. Benzylchlorodimethylsilane (768) is obtained by the coupling of benzyl chloride with dichlorotetramethyl-disilane[632,633]. [Pg.241]

Investigations of silicon-metal systems are of fundamental interest, since stable coordination compounds with low valent silicon are still rare [64], and furthermore, silicon transition-metal complexes have a high potential for technical applications. For instance, coordination compounds of Ti, Zr, and Hf are effective catalysts for the polymerization of silanes to oligomeric chain-silanes. The mechanism of this polymerization reaction has not yet been fully elucidated, but silylene complexes as intermediates have been the subject of discussion. Polysilanes find wide use in important applications, e.g., as preceramics [65-67] or as photoresists [68-83],... [Pg.4]

Uses. There are about forty to fifty organic peroxides commercially available in more than seventy formulations designed for specific applications which include (1) initiators for vinyl monomer polymerizations, and copolymerizations of monomers such as vinyl chloride, ethylene, styrene, vinyl acetate, acrylics, fluoroolefms and buta-dienestyrene (2) curing agents for thermoset polyesters, styrenated alkyds and oils, silicone rubbers and poly allyl diglycol carbonates ... [Pg.681]

Soluble polydiorganosilane homo and copolymers have recently shown great potential in such areas as precursors for the preparation of silicon carbide fibers (1), as photoinitiators in alkene polymerization (2), as photoconductors (3), and as positive or negative self-developing photoresists for photolithographic applications (4). A number of copolydiorganosilane copolymers have been reported recently (5) in which the copolymer contained equal amounts of both monomers in the feed. [Pg.112]

The method of migration polymerization (polyaddition reaction) finds extensive application in the production of silicon-, germanium- and tin-containing hetero-organic polymers 97). [Pg.128]

Commercial hybrid materials, silicon-based, 73 538—540 Commercial hydrazines, physical properties of, 73 565t Commercial hydrolysis, in vinyl alcohol polymerization, 25 609, 612t Commercial immunoassays, for clinical applications, 74 140 Commercial inks, 74 320 Commercial laundering, detersive systems for, 8 413t... [Pg.202]

Siloxane compounds, in vitreous silica manufacture, 22 414 Siloxane materials, 20 240 Siloxane oligomers, in silicone polymerization, 22 555-556 Siloxanols, silylation and, 22 703 Silsesquioxane hybrids, 13 549 Silsesquioxanes, 15 188, 22 589-590 SilvaGas process, 3 696, 697 Silver (Ag), 22 636-667. See also Silver compounds. See Ag entries Argentothiosulfate complexes Batch desilverizing Lead-silver alloys Palladium-silver alloy membranes analytical methods for, 22 650-651 applications of, 22 636-637, 657-662 as bactericide, 22 656, 657, 660 barium alloys with, 3 344 in bimetallic monetary system, 22 647-648 in cast dental gold alloys, 8 307t coke formation on, 5 266 colloidal precipitation color, 7 343t colloidal suspensions, 7 275 color, 7 334, 335... [Pg.843]

Sakurai, H. Yoshida, M. Synthesis of Polysilanes by New Procedures Part 1 Ring-opening Polymerizations and the Polymerization of Masked Disilenes. In Silicon-based Polymers The Science and Technology of their Synthesis and Application-, Jones, R. G., Ando, W., Chojnowski, J., Eds. Kluwer Dordrecht, 2000 pp 375-399. [Pg.644]


See other pages where Polymeric silicones, applications is mentioned: [Pg.411]    [Pg.806]    [Pg.1218]    [Pg.153]    [Pg.314]    [Pg.323]    [Pg.15]    [Pg.117]    [Pg.490]    [Pg.45]    [Pg.411]    [Pg.677]    [Pg.687]    [Pg.691]    [Pg.29]    [Pg.6]    [Pg.7]    [Pg.149]    [Pg.198]    [Pg.201]    [Pg.293]    [Pg.352]    [Pg.527]    [Pg.588]    [Pg.719]    [Pg.369]    [Pg.43]    [Pg.61]    [Pg.99]    [Pg.154]    [Pg.378]    [Pg.263]    [Pg.151]    [Pg.8]    [Pg.649]    [Pg.575]    [Pg.652]    [Pg.652]   
See also in sourсe #XX -- [ Pg.169 ]




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