Oxidation iron chloride

Ethylene oxide Acids and bases, alcohols, air, 1,3-nitroaniline, aluminum chloride, aluminum oxide, ammonia, copper, iron chlorides and oxides, magnesium perchlorate, mercaptans, potassium, tin chlorides, alkane thiols... 

Both the Toth and Alcoa processes provide aluminum chloride for subsequent reduction to aluminum. Pilot-plant tests of these processes have shown difficulties exist in producing aluminum chloride of the purity needed. In the Toth process for the production of aluminum chloride, kaolin [1332-58-7] clay is used as the source of alumina (5). The clay is mixed with sulfur and carbon, and the mixture is ground together, pelletized, and calcined at 700°C. The calcined mixture is chlorinated at 800°C and gaseous aluminum chloride is evolved. The clay used contains considerable amounts of silica, titania, and iron oxides, which chlorinate and must be separated. Silicon tetrachloride and titanium tetrachloride are separated by distillation. Resublimation of aluminum chloride is requited to reduce contamination from iron chloride. 

Ethylamines. Mono-, di-, and triethylamines, produced by catalytic reaction of ethanol with ammonia (330), are a significant outlet for ethanol. The vapor-phase continuous process takes place at 1.38 MPa (13.6 atm) and 150—220°C over a nickel catalyst supported on alumina, siUca, or sihca—alumina. In this reductive amination under a hydrogen atmosphere, the ratio of the mono-, di-, and triethylamine product can be controlled by recycling the unwanted products. Other catalysts used include phosphoric acid and derivatives, copper and iron chlorides, sulfates, and oxides in the presence of acids or alkaline salts (331). Piperidine can be ethylated with ethanol in the presence of Raney nickel catalyst at 200°C and 10.3 MPa (102 atm), to give W-ethylpiperidine [766-09-6] (332). 

A successful procedure for the formation of 2,5-di-t-butylfuran involves reaction of the parent heterocycle with f-butyl chloride in the presence of iron(III) chloride and iron(III) oxide. Iron(III) oxide acts as a hydrogen chloride scavenger and at the same time regenerates the catalyst. Concurrent polymerization normally deactivates the catalyst (82CI(L)603). 

Iron and compounds SPA Iron oxide Eerrous chloride Aluminium refining Steelworks... 

The equation for a net chemical reaction represents the overall transformation of reactants into products. Thus, thallium Ill) ions oxidize iron(II) ions according to Eq. (1-1), and a secondary amine reacts with an aryl chloride as in Eq. (1-2). 

Beryllium and certain compounds Cadmium and certain compounds Carbon tetrachloride Chlorambucil Cyclophosphamide Dimethylcarbamoyl chloride Dimethyl sulphate Ethylene oxide Iron dextran... 

The carbide is an energetic reducant. A powdered mixture with iron oxide and chloride bums violently when ignited, producing molten iron. 

Freeder, B. G. et al., J. Loss Prev. Process Ind., 1988, 1, 164-168 Accidental contamination of a 90 kg cylinder of ethylene oxide with a little sodium hydroxide solution led to explosive failure of the cylinder over 8 hours later [1], Based on later studies of the kinetics and heat release of the poly condensation reaction, it was estimated that after 8 hours and 1 min, some 12.7% of the oxide had condensed with an increase in temperature from 20 to 100°C. At this point the heat release rate was calculated to be 2.1 MJ/min, and 100 s later the temperature and heat release rate would be 160° and 1.67 MJ/s respectively, with 28% condensation. Complete reaction would have been attained some 16 s later at a temperature of 700°C [2], Precautions designed to prevent explosive polymerisation of ethylene oxide are discussed, including rigid exclusion of acids covalent halides, such as aluminium chloride, iron(III) chloride, tin(IV) chloride basic materials like alkali hydroxides, ammonia, amines, metallic potassium and catalytically active solids such as aluminium oxide, iron oxide, or rust [1] A comparative study of the runaway exothermic polymerisation of ethylene oxide and of propylene oxide by 10 wt% of solutions of sodium hydroxide of various concentrations has been done using ARC. Results below show onset temperatures/corrected adiabatic exotherm/maximum pressure attained and heat of polymerisation for the least (0.125 M) and most (1 M) concentrated alkali solutions used as catalysts. 

Presence of 5% of copper(II) chloride caused explosion to occur at 170°C [1]. Of the series of additives copper chromite, copper chloride, nickel oxide, iron oxide, magnesium oxide, the earlier members have the greatest effect in increasing the sensitivity of the perchlorate to heat, impact and friction. 

The effects of various metal oxides and salts which promote ignition of amine-red fuming nitric acid systems were examined. Among soluble catalysts, copperQ oxide, ammonium metavanadate, sodium metavanadate, iron(III) chloride (and potassium hexacyanoferrate(II) with o-toluidine) are most effective. Of the insoluble materials, copper(II) oxide, iron(III) oxide, vanadium(V) oxide, potassium chromate, potassium dichromate, potassium hexacyanoferrate(III) and sodium pentacyanonitrosylferrate(II) were effective. 

Using an organic solution containing 25% Alamine 336 and 15% dodecanol in kerosene, it is possible to separate the metals one after the other by oxidizing iron to Fe(III) and altering the chloride ion concentration by evaporation. This was also the original object of the process. However, it was found that the complete oxidation of iron was complicated and, as the iron in ferro-cobalt and ferro-nickel did not ruin the market value of the products, the process finally used is shown in Fig. 14.9. 

EARS [Enhanced acid regeneration system] A process for recovering hydrochloric acid from the ERMS ilmenite beneficiation process. It may be used also for recovering waste pickle liquor. The acid liquor containing ferrous chloride is evaporated at low temperature to form iron chloride pellets, which are fed to a pyrohydrolysis reactor. This generates hydrochloric acid and iron oxide pellets, which can be used for steel production or disposed of as inert landfill. Developed by E. A. Walpole at the University of Newcastle, Australia, from the early 1990s and piloted by Austpac Gold (now Austpac Resources). 

Corroles are porphyrins which lack the 20-methine group. (7,13-dimethyl-2,3,8,12,17,18-hexa-ethylcorrolato)iron chloride reacts with cyanide to form a low-spin dicyano complex, which is subsequently reduced by excess of cyanide to give (152). The iron in the dicyano complex is still in the 3+ oxidation state, with the reduced correlate as a dinegative radical ligand. ... 

This process is used principally in Europe. It was first developed in 1854 for the production of aniline. Nitrobenzene was reduced to aniline using metallic iron, hence the process was termed the aniline or nitrobenzene process. Iron oxides were formed as unusable, grey/black products. Around 1925, Laux found that addition of iron chloride modified the process so that iron oxides suitable for use as pigments could be produced. With this additive alone, magnetite with a high tinting strength results, i. e. 

Definitely not Metal halides are by no means restricted to group 1 metals. In fact, most metals are able to form halides. Iron chloride, FeCI, and copper chloride, CuCi2, are examples. Figure 18.19 shows only the most common forms of metal compounds. In nature, iron is most commonly found as an oxide, while copper is most commonly found as a sulfide. 

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