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Aluminum , reaction with

A1(CH3NNNCH3), tris(l,3-dimethyltriazeno)aluminum Reaction with CUCI/NH3 8, 4.7.2.1 C H.gAlj... [Pg.302]

Figure 5.4 Main reaction products at 10 bar (a) and adiabatic flame temperatures (b) of aluminum reaction with nitrogen. Figure 5.4 Main reaction products at 10 bar (a) and adiabatic flame temperatures (b) of aluminum reaction with nitrogen.
Aluminum complex greases, obtained by the reaction of aluminum isopropylate with a mixture of benzoic acid and fatty acids. These greases have a remarkable resistance to water, very good adhesion to metallic surfaces, good mechanical stability properties and resistance to temperature. They are less common than the first two types. [Pg.281]

A reaction analogous to the alkylation step of reaction (7.Q) can account for the association of an aluminum species with chain ends ... [Pg.493]

The chlorofluorocarbons react with molten alkah metals and CCI2F2 reacts vigorously with molten aluminum, but with most metals they do not react below 200°C. An exception is the dechlorination of chlorofluorocarbons with two or more carbon atoms in the presence of Zn, Mg, or A1 in polar solvents. A commercial synthesis of chlorotriduoroethylene [79-38-9] employs this reaction ... [Pg.285]

Formamide decomposes thermally either to ammonia and carbon monoxide or to hydrocyanic acid and water. Temperatures around 100°C are critical for formamide, in order to maintain the quaUty requited. The lowest temperature range at which appreciable decomposition occurs is 180—190°C. Boiling formamide decomposes at atmospheric pressure at a rate of about 0.5%/min. In the absence of catalysts the reaction forming NH and CO predominates, whereas hydrocyanic acid formation is favored in the presence of suitable catalysts, eg, aluminum oxides, with yields in excess of 90% at temperatures between 400 and 600°C. [Pg.508]

The other commercially important routes to alkyltin chloride intermediates utilize an indirect method having a tetraalkjitin intermediate. Tetraalkyltins are made by transmetaHation of stannic chloride with a metal alkyl where the metal is typicaHy magnesium or aluminum. Subsequent redistribution reactions with additional stannic chloride yield the desired mixture of monoalkyl tin trichloride and dialkyltin dichloride. Both / -butjitin and / -octjitin intermediates are manufactured by one of these schemes. [Pg.547]

Reaction with AlCl gives lithium aluminum hydtide, which is the main apphcation of hthium hydtide. Reaction with ammonia yields hthium amide... [Pg.297]

In a reversal of the reaction with SiCl, aluminum can be introduced into the framework by reaction of the hydrogen or ammonium form with gaseous AlCl (36). Similarly, reaction with aqueous ammonium fluoroaluminates replaces framework-Si with Al (37). When alumina-bound high siUca 2eohtes are hydrothermaHy treated, aluminum migrates into framework positions and generates catalyticaHy active acid sites (38). The reaction can be accelerated by raising the pH of the aqueous phase. [Pg.451]

Rosin sizing usually involves the addition of dilute aqueous solutions or dispersions of rosin soap size and alum to a pulp slurry (44—46). Although beater addition of either coreactant is permissable, addition of both before final pulp refining is unwise because subsequently exposed ceUulose surfaces may not be properly sized. The size and alum should be added sufficiendy eady to provide uniform distribution in the slurry, and adequate time for the formation and retention of aluminum resinates, commonly referred to as size precipitate. Free rosin emulsion sizes, however, do not react to a significant degree with alum in the pulp slurry, and addition of a cationic starch or resin is recommended to maximize retention of size to fiber. Subsequent reaction with aluminum occurs principally in the machine drier sections (47). [Pg.18]

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). [Pg.391]

The speed of the reaction depends both on the metal and on the alcohol, increasing as electropositivity iacreases and decreasiag with length and branching of the chain. Thus sodium reacts strongly with ethanol, but slowly with tertiary butyl alcohol. The reaction with alkaU metals is sometimes carried out ia ether, ben2ene, or xylene. Some processes use the metal amalgam or hydride iastead of the free metal. Alkaline earth metals and aluminum are often covered with an oxide film which hinders the reaction. [Pg.24]

Methylphenol is converted to 6-/ f2 -butyl-2-methylphenol [2219-82-1] by alkylation with isobutylene under aluminum catalysis. A number of phenoHc anti-oxidants used to stabilize mbber and plastics against thermal oxidative degradation are based on this compound. The condensation of 6-/ f2 -butyl-2-methylphenol with formaldehyde yields 4,4 -methylenebis(2-methyl-6-/ f2 butylphenol) [96-65-17, reaction with sulfur dichloride yields 4,4 -thiobis(2-methyl-6-/ f2 butylphenol) [96-66-2] and reaction with methyl acrylate under base catalysis yields the corresponding hydrocinnamate. Transesterification of the hydrocinnamate with triethylene glycol yields triethylene glycol-bis[3-(3-/ f2 -butyl-5-methyl-4-hydroxyphenyl)propionate] [36443-68-2] (39). 2-Methylphenol is also a component of cresyHc acids, blends of phenol, cresols, and xylenols. CresyHc acids are used as solvents in a number of coating appHcations (see Table 3). [Pg.67]

Aluminum and Hydrogen. Hydrogen [1333-74-0] is the only gas known to be appreciably soluble in soHd or molten aluminum. Hydrogen can be introduced into Hquid aluminum from reaction with moisture present in the furnace atmosphere or the refractories, or with moisture entrapped in the oxide film of the soHd aluminum before melting. The solubiUty of hydrogen in molten and soHd aluminum is shown in Table 6. [Pg.94]

Reactions with Elements and Inorganic Compounds. Aluminum reacts with oxygen [7782-44-7] having a heat of reaction of... [Pg.94]

Reaction with Organic Compounds. Aluminum is not attacked by saturated or unsaturated, aUphatic or aromatic hydrocarbons. Halogenated derivatives of hydrocarbons do not generally react with aluminum except in the presence of water, which leads to the forma tion of halogen acids. The chemical stabiUty of aluminum in the presence of alcohols is very good and stabiUty is excellent in the presence of aldehydes, ketones, and quinones. [Pg.95]

Aluminum acetylsaHcylate is a tasteless, nonbasic, stable, alternative therapeutic salt to aspirin (83). Also called aluminum aspirin, it is an insoluble white to off-white powder prepared by reaction of aluminum isopropoxide with sodium acetylsaHcylate in an organic solvent. The product precipitates from the reaction mixture (83). Standards requke that aluminum aspirin contain not less than the equivalent of 80% aspirin, corresponding to 90% purity on an anhydrous basis. The aluminum oxide assay must be 12—17% (81). [Pg.143]


See other pages where Aluminum , reaction with is mentioned: [Pg.1068]    [Pg.108]    [Pg.1714]    [Pg.1068]    [Pg.108]    [Pg.1714]    [Pg.280]    [Pg.212]    [Pg.16]    [Pg.51]    [Pg.234]    [Pg.39]    [Pg.123]    [Pg.298]    [Pg.515]    [Pg.445]    [Pg.220]    [Pg.137]    [Pg.451]    [Pg.74]    [Pg.411]    [Pg.4]    [Pg.337]    [Pg.348]    [Pg.383]    [Pg.127]    [Pg.143]    [Pg.144]   


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Acid chlorides reaction with lithium aluminum hydride

Acyl compounds reaction with lithium aluminum hydride

Acyl halides, reaction with aluminum

Alcohols from lithium aluminum hydride reaction with

Alkyl halides, reaction with aluminum

Allyl reaction with aluminum

Aluminum alkoxides reaction with alcohols

Aluminum alkyls reaction with propylene

Aluminum alkyls reactions with

Aluminum amides reactions with esters

Aluminum bromide catalyst reaction with oxygen

Aluminum bromide catalyst reaction with water

Aluminum bromide, reaction with oxygen

Aluminum cation reaction with base

Aluminum chloride reaction with benzene

Aluminum clusters, reactions with

Aluminum clusters, reactions with oxygen

Aluminum clusters, reactions with water

Aluminum complexes reactions with hydrocarbons

Aluminum doping reaction with

Aluminum halides reactions with

Aluminum hydrides reactions with

Aluminum hydroxide reaction with hydrochloric acid

Aluminum hydroxide reaction with sulfuric acid

Aluminum iodine reaction with

Aluminum iron oxide reaction with

Aluminum metal reactions with

Aluminum nitrate, reaction with sodium

Aluminum reaction with alkynes

Aluminum reaction with ammonium perchlorate

Aluminum reaction with nitrates

Aluminum reaction with propanol

Aluminum reaction with sulfuric acid

Aluminum reaction with water

Aluminum selenide reaction with nitriles

Aluminum selenolate reaction with esters

Aluminum sulfate reaction with sodium hydroxide

Aluminum, elemental reactions with

Aluminum, sulfatobis catalyst allylstannane reaction with acetals

Aluminum, tris reactions with acyclic enones

Aluminum, wool, reaction with diphenyl

Aluminum, wool, reaction with diphenylmercury to give triphenylaluminum

Aluminum-carbon bonds reactions with

Aluminum-oxygen bonds reactions with

Aluminum-phosphorus bonds reactions with

Bromide aluminum reaction with bromine

Camphor reaction with lithium aluminum hydride

Chloride, aluminum reaction with acyl halides

Diphenylmercury, reaction with aluminum to give triphenylaluminum

Enones reaction with tris aluminum

Epoxides, reaction with aluminum borohydride

Esters, reaction with aluminum borohydride

Halides, alkyl reaction with aluminum hydride reagents

Hydrogen/deuterium reaction with aluminum

Ketones, reaction with aluminum alkoxides

Ketones, reaction with aluminum borohydride

Lactones, reaction with aluminum borohydride

Lithium aluminum hydride reaction with

Lithium aluminum hydride reaction with amides

Lithium aluminum hydride reaction with ethylene

Lithium aluminum hydride reaction with organic halides

Lithium aluminum hydride reaction with protic solvents

Lithium aluminum hydride reaction with water

Lithium aluminum hydride reactions with esters

Lithium aluminum hydride, hazards reaction with 3,4-dichloro-l,2,3,4tetramethylcyclobutene

Lithium aluminum hydride, reaction with aldehydes

Lithium aluminum hydride, reaction with carboxylic acids

Lithium aluminum hydride, reduction reactions with

Methane, reaction with aluminum

Oxygen, reaction with aluminum

Preparation of Highly Reactive Aluminum and Reaction with Aryl Halides

Reaction of Esters with Lithium Aluminum Hydride

Reactions of boron and aluminum hydrides with other coordinated ligands

Sulfonic esters reaction with lithium aluminum hydride

Tetramethyl-1,3-cyclobutanedione, reaction with aluminum chloride

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