Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Acrylic acid Chromium oxide

Acrylic acid, Initiator, Water, 1148 Aluminium chloride, Water, 0062 Barium peroxide, Propane, 0216 1,3-Benzodithiolium perchlorate, 2677 1,1 -Bis(fluorooxy)tetrafluoroethane, 0641 Borane-tetrahydrofuran, 0138 Boron tribromide, Water, 0122 Bromine, Aluminium, Dichloromethane, 0261 Bromine, Tungsten, Tungsten trioxide, 0261 f 1,3-Butadiene, 1480 Calcium oxide, Water, 3937 Chlorine trifluoride, Refractory materials, 3981 Chromium trioxide, Acetic acid, 4242 Copper(II) oxide, Boron, 4281 Diazoacetonitrile, 0675 Dihydroxymaleic acid, 1447 Ethyl azide, 0872... [Pg.170]

The catalyst systems employed are based on molybdenum and phosphorus. They also contain Various additives (oxides of bismuth, antimony, thorium, chromium, copper, zirconium, etc.) and occur in the form of complex phosphomolybdates, or preferably heteropolyacids deposited on an inert support (silicon carbide, a-alumina, diatomaceous earths, titanium dioxide, etc.). This makes them quite different from the catalysts used to produce acrylic acid, which do not offer sufficient activity in this case. With residence times of 2 to 5 s, once-through conversion is better than 90 to 95 per cent, and the molar yield of methacrylic acid is up to 85 to 90 per cent The main by-products formed are acetic add, acetone, acrylic add, CO, C02, etc. The major developments in this area were conducted by Asahi Glass, Daicel, Japan Catalytic Chemical, Japanese Gem, Mitsubishi Rayon, Nippon Kayaku, Standard Oil, Sumitomo Chemical, Toyo Soda, Ube, etc. A number of liquid phase processes, operating at about 30°C, in die presence of a catalyst based on silver or cobalt in alkaline medium, have been developed by ARCO (Atlantic Richfield Co,), Asahi, Sumitomo, Union Carbide, etc. [Pg.210]

AMINOETHYLETHANDIAMINE (111-40-0) Combustible liquid (flash point 208°F/ 98°C oc). An organic base. Ignites spontaneously with cellulose nitrate, and possibly other nitrogen compounds. Silver, cobalt, or chromium compounds may cause explosions. Contact with nitromethane forms a heat-, friction-, and shock-sensitive explosive. Incompatible with acids, acrylates, aldehydes, alcohols, alkylene oxides, caprolactam solution, cresols, organic anhydrides, substituted allyls, epichlorohydrin, glycols, halogenated compounds, isocyanates, ketones, mercury, phenols, strong oxidizers, vinyl acetate. Attacks aluminum, copper, cobalt, lead, tin, zinc, and their alloys. [Pg.84]

HIDROXILAMINA (Spanish) (7803-49-8) A powerful reducing agent. Aqueous solution is a base. Contact with water or steam causes decomposition to ammonium hydroxide, nitrogen, and hydrogen. Contaminants and/or elevated temperatures above (reported at 158°F/70°C and 265°F/129°C) can cause explosive decomposition. Moisture in air or carbon dioxide may cause decomposition. Violent reaction with oxidizers, strong acids, copper(II) sulfate, chromium trioxide, potassium dichromate, phosphorus chlorides, metals calcium, sodium, zinc. Incompatible with carbonyls, pyridine. Forms heat-sensitive explosive mixtures with calcium, zinc powder, and possibly other finely divided metals. Aqueous solution incompatible with organic anhydrides, acrylates, alcohols, aldehydes, alkylene oxides, substituted allyls, carbonyls, cellulose nitrate, cresols, caprolactam solution, epichlorohydrin, ethylene dichloride, glycols, isocyanates, ketones, nitrates, phenols, pyridine, vinyl acetate. Attacks aluminum, copper, tin, and zinc. [Pg.624]


See other pages where Acrylic acid Chromium oxide is mentioned: [Pg.470]    [Pg.470]    [Pg.470]    [Pg.100]    [Pg.102]    [Pg.931]    [Pg.1060]    [Pg.143]    [Pg.144]    [Pg.993]    [Pg.1035]    [Pg.251]    [Pg.170]    [Pg.170]    [Pg.170]    [Pg.192]    [Pg.170]    [Pg.42]    [Pg.388]    [Pg.394]    [Pg.539]    [Pg.571]    [Pg.82]    [Pg.83]    [Pg.384]    [Pg.441]    [Pg.442]    [Pg.456]    [Pg.462]    [Pg.656]    [Pg.1164]   
See also in sourсe #XX -- [ Pg.1020 ]




SEARCH



Acrylic acid, oxidation

Chromium acid

Chromium oxidants

Chromium oxide

Chromium oxids

Oxides chromium oxide

© 2024 chempedia.info