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Alkyl siloxanes

Fig. 11. versus P data and contact hysteresis reported by Chaudhury and Whitesides [471. (a) The data for unmodified PDMS-PDMS contacts. No contact hysteresis was observed, (b) The data for and PDMS modified with alkyl siloxane monolayers, PDMS° -03Si(CH2)9CH3. A weak contact hysteresis was observed, (c) The data for PDMS modified with fluroalkyl siloxane monolayers, PDMS -03Si(CH2)2(CF2)7CF3. A large contact hysteresis was observed. In all cases, the open circles represent the loading data, and the filled circles represent the unloading data. [Pg.102]

Scheme 7 Functionalisation of the mesoporous material prior to the grafting of the complex via an alkyl-siloxane spacer ligand... Scheme 7 Functionalisation of the mesoporous material prior to the grafting of the complex via an alkyl-siloxane spacer ligand...
Microcontact printing (pCP) is a technique that uses an elastomeric stamp with relief on its surface to generate patterned SAMs on the surface of both planar and curved substrates [87,88]. SAMs are highly ordered molecular assemblies that form spontaneously by chemisorption of functionalized long-chain molecules on the surfaces of appropriate substrates [79,89]. Well-established systems of SAMs include alkanethiolates on coinage metals (Au, Ag, Cu) [90] alkyl-siloxanes on hydroxyl-terminated surfaces (Si/Si02, glass) [91] carboxylic and... [Pg.6]

In the case where foam instability is desirable, it is essential to choose surfactants that weaken the Gibbs-Marangoni effect. A more surface-active material such as a poly(alkyl) siloxane is added to destabilize the foam. The siloxane surfactant adsorbs preferentially at the air/liquid interface, thus displacing the original surfactant that stabilizes the foam. In many cases, the siloxane surfactant is produced as an emulsion which also contains hydrophobic silica particles. This combination produces a synergetic effect for foam breaking. [Pg.516]

Chemical transformations in self-assembled monolayers were studied mainly with alkyl-siloxane films on oxidized silica, probably because these layers are more stable than... [Pg.593]

Both gas/solid adsorption and gas/liquid partition chromatography can be used for GC-MS, but GC is by far the most common. Because, in GC, the stationary phase is a liquid, usually a polymer, its vapor pressure will cause a continual low flow, or bleed into the ion source of the mass spectrometer. This bleed, which usually consists of decomposed stationary phase, will produce a spectrum whose intensity increases with column temperature. Stationary phases should therefore be of the high-boiling, low-bleed type. Most currently used stationary phases for routine GC-MS are based on alkyl-polysiloxanes or alkyl-phenyl-polysiloxanes that are chemically bonded to the column wall to increase stability. Columns containing such phases can, in some cases, be used at temperatures of up to 400°C. One advantage, however, to the presence of bleed peaks in the spectrum is that they enable a continual check to be made on the mass spectrometer calibration. For the alkyl siloxanes, ion peaks are present, in decreasing relative abundance, at miz 73, 207, 281, 355, 429,... [Pg.1909]

Higher alkyl siloxanes are not included due to their liquid-crystal characteristics... [Pg.183]

The earliest, and also the most widely studied, SAM systems are those formed by the adsorption of alkyl-siloxanes onto silicon dioxide and by the adsorption of thiols onto noble metal surfaces (Ref. 11 is an extensive review of the subject), but many other SAM systems have been reported. Besides gold, alkanethiols also form ordered, close-packed monolayers on the surfaces of a number of noble metals (including Ag, Cu, Pd, and Pt) and on GaAs, while alkylphosphonic acids and carboxylic acids form SAMs on oxide surfaces. Siloxane monolayers are the most stable, utilizing strong, covalent interactions (Si-O-Si linkages) to tether the molecules to a silanol-terminated oxide surface. However, the chemistry of interaction between the adsorbates and the surface is complex. Silanes (RSiCb) and alkoxysilanes (RSiORj) tend to self-polymerize, which confers additional stability on the... [Pg.3595]

Nunes, S.C., Silva, N.J.O., Hummer, J., Ferreira, RA.S., Almeida, P., Carlos, L.D., and de Zea Bermudez, V. (2012) Water-mediated structural tunability of an alkyl/ siloxane hybrid from amorphous material to lamellar structure or bilamellar superstructure. RSC Adv., 2, 2087-2099. [Pg.602]

Chem. Descrip. Compd. based on polyoxy alkylic siloxanes and cyclic amide... [Pg.1538]

Hydrophobic poly(alkyl siloxane) solutions with high concentrations of hydrophilic 25,35, and 150 nm alumina (AI2O3) nanoparticles deposited via spraying onto glass surfaces displayed a contact angle and hysteresis of 160° and 5°, respectively (Karapanagiotis et al., 2012). The superhydrophobicity was found to be dependent on particle concentration but not on particle size. The latter directly affected the minimum critical particle concentration required to induce superhydrophobicity, which was found to decrease exponentially with specific surface area. [Pg.82]

FIGURE 1.22 Chemical reaction of alkyl-siloxane solgel reaction. (Reproduced with permission from Deng, Q. et al., J. Appl. Polym. Sci., 68, 747, 1998.)... [Pg.26]

Fluoroalkylthio)alkyl siloxanes have been prepared by the addition reaction of vinyl siloxanes with thiols containing a perfluoroalkyl end group [94]. [Pg.530]


See other pages where Alkyl siloxanes is mentioned: [Pg.102]    [Pg.120]    [Pg.285]    [Pg.36]    [Pg.117]    [Pg.96]    [Pg.162]    [Pg.165]    [Pg.139]    [Pg.274]    [Pg.614]    [Pg.515]    [Pg.585]    [Pg.614]    [Pg.120]    [Pg.114]    [Pg.25]    [Pg.25]    [Pg.102]    [Pg.381]    [Pg.203]    [Pg.958]    [Pg.300]    [Pg.354]    [Pg.162]    [Pg.231]    [Pg.602]    [Pg.148]    [Pg.250]    [Pg.116]   
See also in sourсe #XX -- [ Pg.470 ]




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