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Oxides chemical bonding

Chemisoq)tion bonding to metal and metal oxide surfaces has been treated extensively by quantum-mechanical methods. Somoijai and Bent [153] give a general discussion of the surface chemical bond, and some specific theoretical treatments are found in Refs. 154-157 see also a review by Hoffman [158]. One approach uses the variation method (see physical chemistry textbooks) ... [Pg.714]

Quaternary structure (Section 27 22) Description of the way in which two or more protein chains not connected by chemical bonds are organized in a larger protein Quinone (Section 24 14) The product of oxidation of an ortho or para dihydroxybenzene denvative Examples of quinones include... [Pg.1292]

Figure 17 summarizes the avadable sol—gel processes (56). The process on the right of the figure involves the hydrolysis of metal alkoxides in a water—alcohol solution. The hydrolyzed alkoxides are polymerized to form a chemical gel, which is dried and heat treated to form a rigid oxide network held together by chemical bonds. This process is difficult to carry out, because the hydrolysis and polymerization must be carefully controlled. If the hydrolysis reaction proceeds too far, precipitation of hydrous metal oxides from the solution starts to occur, causing agglomerations of particulates in the sol. [Pg.69]

In contrast to most extmsion processes, extmsion coating involves a hot melt, ca 340°C. The thin web cools rapidly between the die and nip even at high linear rates. Both mechanical and chemical bonding to substrates are involved. Mechanical locking of resin around fibers contributes to the resin s adhesion to paper. Some oxidation of the melt takes place in the air gap, thereby providing sites for chemical bonding to aluminum foil. Excessive oxidation causes poor heat-sealing characteristics. [Pg.140]

This chemical bond between the metal and the hydroxyl group of ahyl alcohol has an important effect on stereoselectivity. Asymmetric epoxidation is weU-known. The most stereoselective catalyst is Ti(OR) which is one of the early transition metal compounds and has no 0x0 group (28). Epoxidation of isopropylvinylcarbinol [4798-45-2] (1-isopropylaHyl alcohol) using a combined chiral catalyst of Ti(OR)4 and L-(+)-diethyl tartrate and (CH2)3COOH as the oxidant, stops at 50% conversion, and the erythro threo ratio of the product is 97 3. The reason for the reaction stopping at 50% conversion is that only one enantiomer can react and the unreacted enantiomer is recovered in optically pure form (28). [Pg.74]

Chromium is able to use all of its >d and As electrons to form chemical bonds. It can also display formal oxidation states ranging from Cr(—II) to Cr(VI). The most common and thus most important oxidation states are Cr(II), Cr(III), and Cr(VI). Although most commercial applications have centered around Cr(VI) compounds, environmental concerns and regulations ia the early 1990s suggest that Cr(III) may become increasingly important, especially where the use of Cr(VI) demands reduction and incorporation as Cr(III) ia the product. [Pg.133]

Metals and alloys, the principal industrial metalhc catalysts, are found in periodic group TII, which are transition elements with almost-completed 3d, 4d, and 5d electronic orbits. According to theory, electrons from adsorbed molecules can fill the vacancies in the incomplete shells and thus make a chemical bond. What happens subsequently depends on the operating conditions. Platinum, palladium, and nickel form both hydrides and oxides they are effective in hydrogenation (vegetable oils) and oxidation (ammonia or sulfur dioxide). Alloys do not always have catalytic properties intermediate between those of the component metals, since the surface condition may be different from the bulk and catalysis is a function of the surface condition. Addition of some rhenium to Pt/AlgO permits the use of lower temperatures and slows the deactivation rate. The mechanism of catalysis by alloys is still controversial in many instances. [Pg.2094]

Fig. 2.44. Chemical-bond mapping (a) comparison of EEL spectra recorded from matrix and SiC-fibre with the window for energy filtering shown (b) map of oxidic-bound Si. Fig. 2.44. Chemical-bond mapping (a) comparison of EEL spectra recorded from matrix and SiC-fibre with the window for energy filtering shown (b) map of oxidic-bound Si.
The near-surface region is partially oxidized during OJ bombardment. During the sputter process the chemical bonding of the oxides is broken. Because the binding... [Pg.111]

Another technique that has proved useful in establishing chemical bonding of coupling agents at interfaces is inelastic electron tunneling spectroscopy (ITES). For example. Van Velzen [16] examined 3-(trimethoxysilyl)propanethiol by this technique. Approximately monolayer quantities of this silane were adsorbed on the barrier oxide of an aluminum-aluminum oxide-metal tunneling junction two metals were investigated, lead and silver. It was concluded that the silane is... [Pg.417]


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See also in sourсe #XX -- [ Pg.219 , Pg.273 ]




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