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System aluminum

The system aluminum/water belongs to group II where represents the pitting potential and lies between -0.8 and -1.0 V according to the material and the medium [22,23,36,39,42]. Since alkali ions are necessary as opposite ions to the OH ions in alkalization, the resistance increases with a decrease in alkali ion concentration (see Fig. 2-11). In principle, however, active aluminum cannot be protected cathodically [see the explanation of Eq. (2-56)]. [Pg.58]

Nonferrous metallurgy is as varied as the ores and finished products. Almost every thermal, chemical, and physical process known to engineers is in use. The general classification scheme that follows gives an understanding of the emissions and control systems aluminum (primary and secondary), beryllium, copper (primary and secondary), lead (primary and secondary), mercury, zinc, alloys of nonferrous metals (primary and secondary), and other nonferrous metals. [Pg.500]

Isomerization catalysts were developed along two paths—by Friedel-Crafts halide systems or by dual site heterogeneous catalysts, originating with the commercial introduction of platinum-aluminas for catalytic reforming in the 1940,s. The Friedel-Crafts systems (aluminum chloride-hydrocarbon complexes) were used exclusively during the early stages of... [Pg.146]

The elimination of C1F from a scries of compounds RCH(OH)CCl2CF3 using the system aluminum (1.2 equiv) and lead(II) bromide (O.lequiv) with R = phenyl, 4-methoxyphenyl, 1-mesylindol-3-yl, cyclohexyl or zinc/aluminum(III) chloride with R = CHMePh, phenyl, 3,4-di-chlorophenyl, 1-phenylethyl, cyclohexyl has been described.180181... [Pg.374]

Jeffery EH, Abreo K, Burgess E, et al. 1996. Systemic aluminum toxicity Effects on bone, hematopoietic tissue, and kidney. J Toxicol Environ Health 48 649-665. [Pg.326]

Besides these effects of AlF, on G protein systems, aluminum has its own actions on the phosphoinositide signaling pathway. Aluminum specifically inhibits the Ca2+-dependent enzyme phospholipase C which acts on PIP2. It was found that aluminum chloride inhibited the hydrolysis of PIP2 in a concentration-dependent manner with an IC(50) slightly above 100 pM [56]. The inhibition observed is competitive in nature with the substrate PIP2 [57]. [Pg.114]

H. Sigel, Metal Ions in Biological Systems , Aluminum and its Role in Biology, Vol. 24, Marcel Dekker, New York, 1988. [Pg.2617]

This comprises both new catalysts and new alloys. Here, new fundamental knowledge is needed in order to fully understand the catalyst mechanism and, more importantly, hydride destabilization. Further discussions on some new directions are the subject of other chapters of this book (complex hydrides, amides, destabilized systems, aluminum hydride, nanoparticles and theoretical modeling). [Pg.109]

The above studies all involved only one and two electron systems. And with the exception of the Be high spin excited states (61) none required the use of "Fermi statistics" (wavefunction antisymmetry) in the Monte Carlo simulations. This is of course a prerequisite for multi-electron systems. We have recently carried out REP-QMC simulations on some three-electron systems. Aluminum is probably the simplest. In Table III we show energies for two states of Al and also for Al. ... [Pg.315]

Aluminum precipitation system Aluminum precipitation Unspecified TSDF (not contaminated by agent)... [Pg.45]

Robinson J, Osteryoung RA (1979) An electrochemical and spectroscopic study of some aromatic hydrocarbons in the room temperature molten salt system aluminum cUoride-n-butylpyridinium chloride. J Am Chem Soc 101 323—327... [Pg.488]

FIG. 1 Evidence for self-similarity of the aggregate mass distribution for the aggregating system (aluminum oxide/polyacrylic acid) according to Eq. 26. [Pg.515]

TABLE 8 Fragmentation Characteristics of the System Aluminum Oxide/ Polyacrylic Acid... [Pg.544]

The typical daily dietary AE intake is 10 to 100 mg (Campbell et al., 1957), although absorption is normally minimal. This quantity of dietary AE is more than enough to account for the entire increase of brain AE observed in patients with dialysis dementia. Among 22 such patients, the mean brain AE content was 22 mg/kg dry weight. The normal human brain weighs about 1500 gm and is about 80% water, or 300 gm dry weight. Thus, the total increase in AE content for the whole brain is less than 7 mg in patients with dialysis dementia. Therefore, the entire increase of brain AE in such patients can theoretically be accounted for by dietary aluminum. The increase in body aluminum stores may also be, in part, the result of AE contamination from other sources, such as Al" in dialysate water, dialysis system aluminum pipes, or aluminum leaked from anodes. [Pg.219]

The earlier literature on the effect of metals on rancidity in fats has been well covered by Lea (1939). The accelerating effect of copper and iron on oxidation of fats and fat-containing foods is well established by a wealth of experimental evidence. Other metals, particularly vanadium, cobalt, and manganese, may also be strong pro-oxidants but are less likely to contaminate foods. These metals can accelerate rancidity either in the form of the solid metal in contact with the fat or as water- or fat-soluble salts in heterogenous systems. Aluminum, tin, and zinc have little catalytic activity under most conditions, although tin can act as a surface catalyst for dry fats (Lea, 1946b). [Pg.33]

Acids commonly used in sandstone formations include hydrofluoric-based acids. Full strength mud acid (12wt% HCl + 3wt% HF) has been used to stimulate sandstone reservoirs for several decades [J]. Beeause of the fast reaction of hydrofluoric acid with clay minerals, various retarded mud acids were introduced. In one system, aluminum ehloride was added to mud acid systems to ensure deep acid penetration [4. In a seeond system, boric acid was used to achieve the same goal [5]. Reeently, LuUo and Rae [6] introduced a new acid system, consisting of phosphonic acid and hydrofluoric acid. For high temperature applications, mixtures of organic acids (formic or acetic) and hydrofluoric acids are used [7]. [Pg.329]

Another use for silane treatment as well as for organics such as steric acid or octadecanoic acid has been to protect the surface of the particles from hydration so that they can be processed in a water-based system. Aluminum nitride, some of the ceramic superconductors, and materials like lithium aluminate fall into this category. The use of an organic "shield to produce a monolayer of hydrophobic material on the surface has been reviewed in several articles. [Pg.66]

Selective leaching or dealloying is the selective removal of one element from an alloy by corrosion processes. The most common example is the selective removal (dezincification) of zinc in brass alloys. Dezincification may either be plug-type or uniform. In other alloy systems, aluminum, iron, cobalt, nickel, chromium, and other elements may be selectively removed [49]. Little work has been done in differentiating susceptibility of selective leaching of alloys in synthetic and naturtil seawater [6]. [Pg.370]


See other pages where System aluminum is mentioned: [Pg.389]    [Pg.127]    [Pg.172]    [Pg.238]    [Pg.284]    [Pg.379]    [Pg.185]    [Pg.2933]    [Pg.79]    [Pg.164]    [Pg.301]    [Pg.240]    [Pg.506]    [Pg.127]    [Pg.172]    [Pg.223]    [Pg.240]    [Pg.5242]    [Pg.26]    [Pg.506]    [Pg.109]    [Pg.1934]    [Pg.414]    [Pg.349]    [Pg.87]    [Pg.225]   
See also in sourсe #XX -- [ Pg.237 ]




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