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Thickness siloxane

Thick Siloxane Films from Tetraethoxysilane on Silicon... [Pg.333]

To investigate the elastic properties resulting from ether-functionalized silylester condensates, the diethoxymethyl derivatives were used in 1 1-mixtures with the commercial stone consolidant F510 of Remmers Bauchemie to prepare thick siloxane films in Petri dishes. Fig. lb shows a photograph of the polycondensate obtained from F510 modified with (3-methoxypropyl)diethoxymethylsilane. In comparison with the film produced by hydrolysis and condensation of the unmodified consolidant (Fig. la), considerably less shrinking fissures are observed. [Pg.529]

Rahman, M. Amsarani, R. Mooney, D. A. MacElroy, J. M. D. Dowling, D. P., Effect of Process Parameters on Chemistry, Growth Rate and Nano-Sized Particulate Formation of Atmospheric Plasma Deposited, nm Thick Siloxane Coatings. J. Nanosci. Nanotech. 2009, 9,3506-3513. [Pg.137]

The finite size effects in the contact between a spherical lens of polyurethane and a soft flat sheet of crosslinked polyfdimethyl siloxane) (PDMS) has been addressed by Falsafi et al. [37]. They showed that for deformations corresponding to contact diameters larger than the sheet thickness, the compliance of the system was affected by the glass substrate supporting the soft sheet. In order to minimize the finite size effects in the adhesion measurement of small elastomeric lenses, Falsafi et al. [38] and Deruelle et al. [39] used relatively thick elastic sheets to support their samples. [Pg.89]

Another approach to molecular assembly involves siloxane chemistry [61]. In this method, the electrically or optically active oligomers are terminated with tii-chlorosilane. Layers are built up by successive cycles of dip, rinse, and cure to form hole transport, emissive, and electron transport layers of the desired thicknesses. Similar methods have also been used to deposit just a molecular monolayer on the electrode surface, in order to modify its injection properties. [Pg.223]

Fig. 4. Data of Auroy et al. [25] on polydimethyl-siloxane chains covalently grafted in the interior of a silica porous medium. L is the measured layer thickness from neutron scattering d is the average spacing per chain from the grafting density. The format of the plot is suggested by Eq. 5. The linearity of that relation is seen in these data... Fig. 4. Data of Auroy et al. [25] on polydimethyl-siloxane chains covalently grafted in the interior of a silica porous medium. L is the measured layer thickness from neutron scattering d is the average spacing per chain from the grafting density. The format of the plot is suggested by Eq. 5. The linearity of that relation is seen in these data...
Fused-silica capillary GC column, 30 m x 0.25-mmi.d., coated with 5% phenyl (equiv.) polysilphenylene-siloxane (0.25- um film thickness)... [Pg.1169]

Since crosslinking of the polymer occurs as the result of the initial formation of silyl radicals, the siloxane polymer containing both phenyldisilanyl units and functional groups which undergo radical polymerization should produce solid material whatever the thickness of the films. To ascertain this, we have examined the photochemical behavior of the polymers 2-4. [Pg.213]

In thick samples, a boron oxide/boron carbide crust has been detected on the surface of the polymer. This inorganic surface layer has a shielding effect on the inner polymer layers, further enhancing the thermal stability of the material. Poly(m-carborane-siloxane)s have therefore been considered as surface coatings for organic materials, providing protection from erosion effects. [Pg.111]

Distil through a Vigreux column in a N2 atmosphere maintaining the oil bath temperature thermostated at 135-140°. Check the purity by H NMR [CCI 3. 5 single peak at 13cps from Me4Si. Likely impurities are siloxane hydrolysis products. The azide is thermally stable even at 200° when it decomposes slowly without explosive violence. AH the same it is advisable to carry out the distillation behind a thick... [Pg.445]

Although it was demonstrated that the siloxane component of these materials migrates to the surface (top 50 A) during cure, 5), there is no evidence that this creates a concentration gradient of siloxane throughout the entire sample thickness. However,... [Pg.93]

As an example, gas flow from a cola beverage was analyzed and calibration of benzalde-hyde was performed as described in Support Protocol 1. A 100-pm-thick polydimethyl-siloxane (PDMS) SPME fiber was used to extract the gas flow from the cola beverage. Since equilibrium with the flow concentration was determined to occur within 5 min for the slowest-equilibrating compound, the fiber was exposed to the gas flow for 5 min and then desorbed in the injection port of a GC/MS. A 0.01 %... [Pg.1079]

Films of y-APS on steel do not contain siloxanes if veiy thin, but they become detectable as the thickness increases. [Pg.342]

Dawkins and Taylor109 dispersed poly(methyl methacrylate) (PMMA) or polystyrene (PS) particles in n-alkanes stabilized by AB block copolymers of styrene and dimethyl-siloxane. In these cases, styrene blocks act as anchors and dimethylsiloxane blocks give a surface layer. The thickness 6 of the dimethylsiloxane layer was determined by viscosity measurements as a function of the molecular weight of dimethylsiloxane blocks. [Pg.53]

Careful XPS analysis of a series of poly(dimethylsiloxane-urea-urethane) multiblock copolymers demonstrated that, as well as a surface layer of siloxane, there was a layer enriched in the hard block immediately beneath this. The thickness of both these layers depended on the molecular weights of the soft and hard block segments, respectively112. Annealing of these copolymers increased the thickness of both layers. The same authors have also shown that the thickness of these layers of hard and soft blocks could be modified by use of solvent mixtures which selectively precipitate the polar hard block during film formation by solvent casting113. [Pg.2236]


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See also in sourсe #XX -- [ Pg.266 ]




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Film thickness siloxane

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