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Silanes coating surfaces

As was already demonstrated in Sect. 5.3 for LC films adsorbed on silane coated surfaces, the intrinsic interface sensitivity of SHG can be further exploited to study the ordering of LG molecules deposited on photo-modified PVCN films [57], In this way some of the ideas discussed in the previous... [Pg.70]

Auger electron spectroscopy (AES) activates the sample through electrons producing ionization of atoms on the outer silane layer. During refilling of this hole by an outer electron, the energy released can be transferred to a third electron that leaves the solid and can be detected. By this method, two-dimensional silane-coated surfaces can be analyzed [27]. Although it may be assumed that comparable processes wiU take place on the surfaces of mineral fillers, AES cannot be used for analysis since mineral fillers are three-dimensional. [Pg.73]

There are other spectroscopy methods also available for characterizing silane-coated surfaces such as SSIMS (static secondary ion mass spectrometry), AFM... [Pg.75]

Fig. 2.3.11 Left the ingress of a hydrophobic silane coating into building sandstone. Right subsequent water ingress and pumping through a treated surface. Fig. 2.3.11 Left the ingress of a hydrophobic silane coating into building sandstone. Right subsequent water ingress and pumping through a treated surface.
Therefore, once the silane coated glass fibers are in contact with uncured resins, the R-groups on the fiber surface react with the functional groups present in the polymer resin, such as methacrylate, amine, epoxy and styrene groups, forming a stable covalent bond with the polymer (Fig. 5.3(d)). It is essential that the R-group... [Pg.175]

These dendrimers were then used to achieve a stable coating of amino-silanized glass surfaces with NH2-modified DNA-probes (see Fig. 10). DNA chips which were prepared according to this procedure exhibited several advantages regarding the signal-to-noise ratio and their reliability over commercial chips prepared by conventional linking. [Pg.49]

When a silane coated wafer was baked at 400°C and examined by ESCA for surface elements it showed almost a total loss of carbon and amine nitrogen. We view this, therefore, as evidence that organic silane will not survive the bake and Si02 will remain. Results are presented in Table VI. [Pg.113]

Many surface modifications are used with aluminium hydroxide, which responds to both silane and fatty acid treatments. Special proprietary silane coatings seem to be preferred for polypropylene applications [99]. Despite the production being water based, the preference seems to be for dry coating procedures. [Pg.100]

Figure 2. The change in HAPS (as N Is), aluminium, and calcium concentrations after aqueous extraction. The analysis angle was 15°. U = uncoated surface C = coated surface W= the silanized surface after extraction with warm water at 50°C H = the silanized surface after extraction with hot water at IGO°C. Figure 2. The change in HAPS (as N Is), aluminium, and calcium concentrations after aqueous extraction. The analysis angle was 15°. U = uncoated surface C = coated surface W= the silanized surface after extraction with warm water at 50°C H = the silanized surface after extraction with hot water at IGO°C.
The acoustic energies of the pulses are shown in Fig. 11 and indicate the stress levels at which fracture has occurred in fibers of the same diameter. It is interesting to note here that fibers treated by the polymeric silane produce failure pulses at a higher energy than the untreated fibers. The protective effect of the polymeric silane coating in healing some surface flaws can be deduced from this observation. This effect is not significant when the monomeric silane is used. [Pg.489]

The deposition of the silane in the loading step has been studied. The surface loading was correlated to the specific surface area of the silica rather than the hydroxyl content. Part of the deposition, therefore, is non-hydroxyl specific. The above reaction schemes, however, indicate the crucial role of the hydroxyls in the consolidation of the silane coating on the surface. [Pg.255]

Other applications use self-assembling fibers to coat materials. For example, preassembled peptide amphiphiles have been covalently immobilized on titanium implant surfaces via a silane layer (Sargeant et al., 2008). Primary bovine artery endothelial cells or mouse calvarial preosteoblastic cells spread on these coated surface and proliferated to a far greater extent than on samples where the peptide amphiphiles had been drop cast onto the metal surface. This study therefore suggests that covalent attachment is required in order to prevent fibers lifting from the coated surface and to encourage maximal cell growth. [Pg.203]

Nevertheless, with regard to filler treatment and limestone impregnation, it is still considered difficult to coat calcium carbonate with silicone. As shown in Table 1, the commercial monomeric silanes that are used for coating the surfaces of fillers nowadays are not effective for coating calcite [19, 20, 21]. The idea that the production of a silicone-coated surface is difficult may result from the misconception that attachment of high silicone polymers to calcium carbonate is equally problematic. The issue of attachment of silicone to the mineral surfaces has still not been finally resolved [62]. [Pg.841]

Various surface modifying operations such as silane coating, maleation, oxidation, surface coating have a noticeable effect on surface energy. [Pg.274]

The first Pz immunosensor to be used directly in solution incorporated an inorganic silane layer for immobilisation [10]. Incorporating results from chromatographic studies, which at the time had recently shown the high reactivity of silane-modified surfaces for proteins, the authors coated their ST-cut crystals with trimethoxyorganosilane. [Pg.247]

A sensor for the detection of human granulocytes was also reported by the authors [47]. Immobilisation was carried out using silane, protein A and polyethyleneimine. Similar results were observed for each method but the later showed better stability. The antigen was measured linearly in blood from 2x10 to 3x10 cells. The antibody-coated surface was stable for 8 weeks without detectable loss in activity. Regeneration was not possible since removal of all the bound cells even under harsh conditions did not occur. [Pg.268]

E. Sacher, A comparison of Ycrit and % for silane coatings, in Silylated Surfaces Midland... [Pg.687]


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See also in sourсe #XX -- [ Pg.240 ]




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