Aluminum studies

Pi TW, Liu Ch, Hwang J (2006) Surface electronic structure of Ca-deposited tris (8-hydroxyquinolato) aluminum studied by synchrotron radiation photoemission. J Appl Phys 99 123712... 

Gorsky JE, Dietz AA, Spencer H, et al. 1979. Metabolic balance of aluminum studied in six men. Clin Chem 25 1739-1743. 

The authors are grateful to the numerous talented postgraduate and postdoctoral researchers who have contributed to our zirconium, magnesium, and aluminum studies described herein, and to industrial collaborators (ICI Acrylics, now Lucite International, and BASF, in particular) who have encouraged our stereoselective acrylate polymerization catalyst program at various stages. 

These studied have been highlighted in John and Hong s presentation [28, 31-33, 35-39] and the publications of the new anodized aluminum study with Mansfeld et al [38, 39]. 

Aluminum Study and Supplier Qualification - Part one and Part Two", Lam Research Confidential Technical Repwrt, May 31, 2003. 

Nelson et al. [34] determined from void shapes that the ratio 7100/7110 was 1.2, 0.98 and 1.14 for copper at 600°C, aluminum at 550°C, and molybdenum at 2000°C, respectively, and 1.03 for 7100/7111 for aluminum at 450°C. Metal tips in field emission studies (see Section VIII-2C) tend to take on an equilibrium faceting into shapes agreeing fairly well with calculations [133]. 

Evans R, Smith I, Munz W D, Williams K J P and Yanwood J 1996 Raman microscopic studies of ceramic coatings based on titanium aluminum nitride ICORS 96 XVth Int. Conf. on Raman Spectroscopy ed S A Asher and P B Stein (New York Wiley) pp 596-7... 

Jesson B J, Foley M and Madden P A 1997 Thermal properties of the self-interstitlal In aluminum an ab initio molecular-dynamics study Pbys. Rev. B 55 4941-6... 

In the early 1950s Karl Ziegler then at the Max Planck Institute for Coal Research in Germany was studying the use of aluminum compounds as catalysts for the oligomer ization of ethylene... 

Fluorosulfuric acid can be very corrosive. A study of the corrosive properties of fluorosulfuric acid during preparation and use showed carbon steel to be acceptable up to 40°C, stainless steel up to 80°C, and aluminum alloys up to 130°C (52). 

In addition, boron, aluminum, and gallium tris(triduoromethanesulfonates) (tridates), M(OTf)2 and related perduoroalkanesulfonates were found effective for Friedel-Crafts alkylations under mild conditions (200). These Lewis acids behave as pseudo haUdes. Boron tris(tridate) shows the highest catalytic activity among these catalysts. A systematic study of these catalysts in the alkylation of aromatics such as benzene and toluene has been reported (201). 

Reactions of HCl and nitrides, borides, silicides, germanides, carbides, and sulfides take place at significant rates only at elevated (>650° C) temperatures. The products are the metal chlorides and the corresponding hydrides. The reactions most studied are those involving nitrides of aluminum, magnesium, calcium, and titanium, where ammonia (qv) is formed along with the corresponding metal chloride. 

Heterogeneous Catalysis. The main discovery of the 1980s was the use of titanium sihcaUte (TS-1) a synthetic zeoHte from the ZSM family containing no aluminum and where some titanium atoms replace siUcon atoms in the crystalline system (Ti/Si = 5%) (33). This zeoHte can be obtained by the hydrolysis of a siUcate and an alkyl titanate in the presence of quaternary ammonium hydroxide followed by heating to 170°C. Mainly studies have been devoted to the stmcture of TS-1 and its behavior toward H2O2 (34). The oxidation properties of the couple H2O2/TS-I have been extensively developed in... 

The synthesis of 2,4-dihydroxyacetophenone [89-84-9] (21) by acylation reactions of resorcinol has been extensively studied. The reaction is performed using acetic anhydride (104), acetyl chloride (105), or acetic acid (106). The esterification of resorcinol by acetic anhydride followed by the isomerization of the diacetate intermediate has also been described in the presence of zinc chloride (107). Alkylation of resorcinol can be carried out using ethers (108), olefins (109), or alcohols (110). The catalysts which are generally used include sulfuric acid, phosphoric and polyphosphoric acids, acidic resins, or aluminum and iron derivatives. 2-Chlororesorcinol [6201-65-1] (22) is obtained by a sulfonation—chloration—desulfonation technique (111). 1,2,4-Trihydroxybenzene [533-73-3] (23) is obtained by hydroxylation of resorcinol using hydrogen peroxide (112) or peracids (113). 

Iron—Aluminum and Iron—Aluminum—Silicon Alloys. The influence of aluminum on the physical and magnetic properties of iron is similar to that of silicon, ie, stabilization of the bcc phase, increased resistivity, decreased ductility, and decreased saturation magnetization, magnetocrystalline anisotropy, and magnetostriction. Whereas Si—Ee alloys are well estabHshed for electrical appHcations, the aluminum—iron alloys have not been studied commercially. However, small (up to ca 0.3%) amounts of A1 have been added to the nonoriented grades of siHcon steel, because the decrease in ductiHty is less with A1 than with Si. 

With appropriately substituted oxetanes, aluminum-based initiators (321) impose a degree of microstmctural control on the substituted polyoxetane stmcture that is not obtainable with a pure cationic system. A polymer having largely the stmcture of poly(3-hydroxyoxetane) has been obtained from an anionic rearrangement polymerisation of glycidol or its trimethylsilyl ether, both oxirane monomers (322). Polymerisation-induced epitaxy can produce ultrathin films of highly oriented POX molecules on, for instance, graphite (323). Theoretical studies on the cationic polymerisation mechanism of oxetanes have been made (324—326). 

Inositols, ie, hexaliydrobenzenehexols, are sugars that have received increasing study and are useful in the treatment of a wide variety of human disorders, including vascular disease, cancer, cirrhosis of the Hver, frostbite, and muscular dystrophy (269). Myoinositol esters prepared by reaction with lower fatty acid anhydrides are useful as Hver medicines and nonionic surfactants the aluminum and ammonium salts of inositol hexasulfate are useful anticancer agents (270). Tetraarjloxybenzoquinones are intermediates in the preparation of dioxazine dyes (266,271). The synthesis of hexakis(aryloxy)benzenes has also beenpubUshed (272). 

The earliest reported reference describing the synthesis of phenylene sulfide stmctures is that of Friedel and Crafts in 1888 (6). The electrophilic reactions studied were based on reactions of benzene and various sulfur sources. These electrophilic substitution reactions were characterized by low yields (50—80%) of rather poorly characterized products by the standards of 1990s. Products contained many by-products, such as thianthrene. Results of self-condensation of thiophenol, catalyzed by aluminum chloride and sulfuric acid (7), were analogous to those of Friedel and Crafts. 

Much work has been done on the structure of the metal alkoxides (49). The simple alkaU alkoxides have an ionic lattice and a layer stmcture, but alkaline earth alkoxides show more covalent character. The aluminum alkoxides have been thoroughly studied and there is no doubt as to their covalent nature the lower alkoxides are associated, even in solution and in the vapor phase. The degree of association depends on the bulkiness of the alkoxy group and can range from 2 to 4, eg, the freshly distilled isopropylate is trimeric (4) ... 

Hydrates. Aluminum sulfate hydrates, Al2(SO H20, where n ranges from 0 to 27 have been reported (3—6). Relative decreasiag vapor pressure studies iadicate the presence of an octadecahydrate, hexadecahydrate, dodecahydrate, dihydrate, and the anhydrous salt, assumiag that basic aluminum sulfates are not formed duriag the dehydration (3). 

Aluminum sulfate is a starting material in the manufacture of many other aluminum compounds. Aluminum sulfate from clay could potentially provide local sourcing of raw materials for aluminum production. Processes have been studied (24) and the relative economics of using clay versus bauxite have been reviewed (25). It is, however, difficult to remove impurities economically by precipitation, and purification of aluminum sulfate by crystallization is not practiced commercially because the resulting crystals are soft, microscopic, and difficult to wash effectively on a production scale (26—28). 

Aluminum chloride hydroxide [1327-41 -9] [10284-64-7], AlQ(OH)2 [14215-15-7], AlQ2(OH), products, commonly known as polyaluminum chlorides (PAG), are used for a wide variety of industrial appHcations. Other names for PAG are basic aluminum chloride, polybasic aluminum chloride, aluminum hydroxychloride, aluminum oxychloride, and aluminum chlorohydrate. The presence of polymeric, aluminum-containing cations, the distribution of which can differ gready, typifies PAG products. Although the formation of polynuclear aluminum species in solution has been studied for over a century, there is stiU much controversy concerning aluminum polymerization reactions and the resulting product compositions. 

The vapor-phase conversion of aniline to DPA over a soHd catalyst has been extensively studied (18,22). In general, the catalyst used is pure aluminum oxide or titanium oxide, prepared under special conditions (18). Promoters, such as copper chromite, nickel chloride, phosphoric acid, and ammonium fluoride, have also been recommended. Reaction temperatures are usually from 400 to 500°C. Coke formed on the catalyst is removed occasionally by burning. In this way, conversions of about 35% and yields of 95% have been reported. Carba2ole is frequently a by-product. 

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