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Silane coupling agents preparation

Table 5. Preparation of poyoxazoline silane coupling agents... Table 5. Preparation of poyoxazoline silane coupling agents...
Ethylene-vinyl acetate Fetterman [37] reinforced compounded ethylene-vinyl acetate (EVA) copolymer by using short hbers and found that silane coupling agents were effective at establishing improved hber-matrix adhesion. Das et al. [38] prepared carbon fiber-filled conductive composites based on EVA and studied the electromagnetic interference shielding effectiveness of the composites. [Pg.354]

A second industrially important field in which silanols play a vital role is in the preparation of polysiloxanes, often known as silicones. As in the case of silane coupling agents, there is a vast literature available on the topic of polysiloxanes, and only the most general discussion will be given here, concentrated on the reactions that involve silanols. [Pg.152]

Weetall, H.H. (1993) Preparation of immobilized proteins covalently coupled through silane coupling agents to inorganic supports. Applied Biochemistry and Biotechnology, 41, 157-188. [Pg.107]

Figure 14.25 The preparation of highly controlled fluorescent silica nanoparticles can be done by first polymerizing APTS that has been covalently modified with an amine-reactive dye to form fluorescent core particles. The core then is capped by a shell of silica by polymerization of TEOS. The shell layer can be further derivatized with silane coupling agents to provide functional groups for conjugation. Figure 14.25 The preparation of highly controlled fluorescent silica nanoparticles can be done by first polymerizing APTS that has been covalently modified with an amine-reactive dye to form fluorescent core particles. The core then is capped by a shell of silica by polymerization of TEOS. The shell layer can be further derivatized with silane coupling agents to provide functional groups for conjugation.
The hydrophilic SiO substrate)static water contact angle 0=3O°) was prepared by vapor-deposited SiO onto a Formvar substrate[4], with which an electron microscope grid(200-mesh) was covered. The relatively hydrophobic siliconized substrate(0=9O°) was also prepared by surface siliconized treatment a collodion-covered electron microscope grid was dipped into an aqueous solution of silane coupling agent. [Pg.12]

Our interest in silane coupling agents and in the preparation of silicates has led us to study the mechanisms involved in the various reactions. In a previous paper, we investigated the kinetics and mechanism of the alcoholysis of TMOS [13]. This present work studies the effects of changing the substituents on a para-substituted phenyl attached directly to the alkoxysilane. The alkoxysilane silanes used have only one alkoxy group present to eliminate complications from a competing second or third alcoholysis reaction. The resulting Hammett plot yields additional information on the mechanism of this reaction. [Pg.162]

The kinetics of the acid catalyzed hydrolysis of ethoxysilanes has been studied. Each of the silanes that were used had a phenyl or para-substituted phenyl group attached to the silicon atom. This permitted a study of the linear free energy relationships of this reaction. The reaction is of interest because of its role in silane coupling agent chemistry, in the preparation of zinc-rich silicate coatings, in the sol-gel process and in the preparation of silicones in general. [Pg.178]

SUica particles can be coated by the silane coupling agent APS in the reaction medium to obtain stable colloids. These systems can be used to further bind relevant groups to the particle surface [48,51,52]. Quantitative Si NMR spectroscopy appears to be a valuable tool in characterizing a new kind of stable colloidal particles synthesized from a mixture of the alkoxides APS and TES. These monodisperse, spherical particles can aheady be prepared with a low polydispersity and contain APS molecules distributed through an important part of the bulk of the particle. It would be interesting to see whether this method is also applicable to other mixtures of alkoxides. More work concerning the characterization of these new systems has to be done [50]. [Pg.79]


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See also in sourсe #XX -- [ Pg.120 ]




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