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Reactive layer

Desmarescaux, P. M. et. al., inventor, U.S. 2005/0113279 Detergent tablet comprising two layers reactive during dissolution, separated by a barrier layer, Eurotab SA, 2005. [Pg.416]

Pinnavaia et al. described the bonding of the pillars to the hectorite clay sheets, upon calcination, as a layer cross-linking mechanism [57]. Si and Al MAS-NMR data on Al-pillared smectite clays indicated the existence of two mechanisms for the linking of the pillars to the clay sheets. It was shown that the layer composition of the host clay plays a very important role in determining the layer reactivity upon heating. [Pg.281]

At that time, Plee et al. stated that the layer reactivity is solely related to the origin of the layer charge, and only occurs in case of tetrahedrally charged smectites [58]. Later, however, Pinnavaia et al. proved that the mechanism of cross-linking was also possible for the octahedrally substituted fluorohectorite clay [57]. present in the former clay, was found to be responsible for the labiliza-tion of the Si-0 bonds of the tetrahedral layer (40). This promotes the linking between the host layers and the pillars to form Siday-O-Alpmar covalent bonds by an inversion of the Si04-tetrahedrons. This mechanism of cross-linking for fluorohectorite is represented in Fig. 14. [Pg.282]

Enhanced wettabiMy/ oompalHity Cross-linked bouncbry layer Reactive graft sites... [Pg.411]

Thin-film polyimide-based implants use the polymer as both the structural and insulation material. They have been micromachined with multilayer metallization [54] for use as acute and chronic extracellular recording electrodes, and sieve and cuff regeneration electrodes. Thin-film metal layers (approximately 200-300 nm thickness) are sandwiched between the polymer layers. Reactive ion etching in oxygen opens contacts to the electrodes. This dry etch also defines the probe shape (Fig. 7). [Pg.169]

Madey and co-workers followed the reduction of titanium with XPS during the deposition of metal overlayers on TiOi [87]. This shows the reduction of surface TiOj molecules on adsorption of reactive metals. Film growth is readily monitored by the disappearance of the XPS signal from the underlying surface [88, 89]. This approach can be applied to polymer surfaces [90] and to determine the thickness of polymer layers on metals [91]. Because it is often used for chemical analysis, the method is sometimes referred to as electron spectroscopy for chemical analysis (ESCA). Since x-rays are very penetrating, a grazing incidence angle is often used to emphasize the contribution from the surface atoms. [Pg.308]

Black phosphorus is formed when white phosphorus is heated under very high pressure (12 000 atmospheres). Black phosphorus has a well-established corrugated sheet structure with each phos phorus atom bonded to three neighbours. The bonding lorces between layers are weak and give rise to flaky crystals which conduct electricity, properties similar to those ol graphite, it is less reactive than either white or red phosphorus. [Pg.210]

The reactivity of the transition metals towards other elements varies widely. In theory, the tendency to form other compounds both in the solid state (for example reactions to form cations) should diminish along the series in practice, resistance to reaction with oxygen (due to formation of a surface layer of oxide) causes chromium (for example) to behave abnormally hence regularities in reactivity are not easily observed. It is now appropriate to consider the individual transition metals. [Pg.369]

As with polyesters, the amidation reaction of acid chlorides may be carried out in solution because of the enhanced reactivity of acid chlorides compared with carboxylic acids. A technique known as interfacial polymerization has been employed for the formation of polyamides and other step-growth polymers, including polyesters, polyurethanes, and polycarbonates. In this method the polymerization is carried out at the interface between two immiscible solutions, one of which contains one of the dissolved reactants, while the second monomer is dissolved in the other. Figure 5.7 shows a polyamide film forming at the interface between an aqueous solution of a diamine layered on a solution of a diacid chloride in an organic solvent. In this form interfacial polymerization is part of the standard repertoire of chemical demonstrations. It is sometimes called the nylon rope trick because of the filament of nylon produced by withdrawing the collapsed film. [Pg.307]

Finally, the metallisation layer usually requires patterning, which can be done by reactive ion etching (RIE) or back-sputtering. The two processes are similar. In both techniques accelerated ions hit the substrate and forcibly detach atoms or molecules from the surface. RIE uses reactive gases such as chlorine, Cl or trichlorofluoromethane [75-69-4] CCl E. Inert gases such as argon or neon are used in back-sputtering. [Pg.349]

Interfdci l Composite Membra.nes, A method of making asymmetric membranes involving interfacial polymerization was developed in the 1960s. This technique was used to produce reverse osmosis membranes with dramatically improved salt rejections and water fluxes compared to those prepared by the Loeb-Sourirajan process (28). In the interfacial polymerization method, an aqueous solution of a reactive prepolymer, such as polyamine, is first deposited in the pores of a microporous support membrane, typically a polysulfone ultrafUtration membrane. The amine-loaded support is then immersed in a water-immiscible solvent solution containing a reactant, for example, a diacid chloride in hexane. The amine and acid chloride then react at the interface of the two solutions to form a densely cross-linked, extremely thin membrane layer. This preparation method is shown schematically in Figure 15. The first membrane made was based on polyethylenimine cross-linked with toluene-2,4-diisocyanate (28). The process was later refined at FilmTec Corporation (29,30) and at UOP (31) in the United States, and at Nitto (32) in Japan. [Pg.68]

The likelihood that materials will produce local effects in the respiratory tract depends on their physical and chemical properties, solubiHty, reactivity with fluid-lining layers of the respiratory tract, reactivity with local tissue components, and (in the case of particulates) the site of deposition. Depending on the nature of the material, and the conditions of the exposure, the types of local response produced include acute inflammation and damage, chronic... [Pg.229]


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