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Iron oxide process continuous

III.B.2), complexes with manganese, chromium, as well as second- and third-row transition metal ions (e.g., ruthenium) oxidation reactions with dioxygen alone or with other peroxides (e.g., ferf-butyl-peroxide) the stabilization and spectroscopic characterization of mononuclear superoxo, peroxo, and oxo complexes other catalytic processes (e.g., the iron-catalyzed aziridination), enantioselective reactions with chiral bispidine ligands and the iron oxidation chemistry continues to produce novel and exciting results. [Pg.690]

The Fischer-Tropsch process requires synthesis gas in which the total sulfur does not exceed 2.0 mg./cubic meter. This purification was done in two stages (1) Removal of hydrogen sulfide and (2) removal of organic sulfur. The removal of hydrogen sulfide is almost universally carried out by the well known iron oxide process. At the Luetzkendorf plant, the so-called Alkazid process had been installed, in which a solution of an alkaline organic compound absorbs the hydrogen sulfide, which is then continuously stripped from the solution by steam. At Luetzkendorf, the evolved hydrogen sulfide was converted into elemental sulfur. [Pg.119]

Removal of larger amounts of hydrogen sulfide from gas streams requires continuous processes, such as the Ferrox process or the Stretford process (Mokhatab et al., 2006 Speight, 2007, 2008). The Ferrox process is based on the same chemistry as the iron oxide process except that it is fluid and continnons. The Stretford process employs a solution containing vanadinm salts and anthraqui-none disulfonic acid (Maddox, 1974). [Pg.709]

DR Processes Under Development. The 1990s have seen continuous evolution of direct reduction technology. Short-term development work is focusing on direct reduction processes that can use lower cost iron oxide fines as a feed material. Use of fines can represent a 20 30/1 (20%) savings in DRI production cost compared to use of pehets or lump ore. Some examples of these processes include FASTMET, Iron Carbide, CIRCOFER, and an improved version of the EIOR process. [Pg.431]

In the Bnchamp process, nitro compounds are reduced to amines in the presence of iron and an acid. This is the oldest commercial process for preparing amines, but in more recent years it has been largely replaced by catalytic hydrogenation. Nevertheless, the Bnchamp reduction is still used in the dyestuff industry for the production of small volume amines and for the manufacture of iron oxide pigments aniline is produced as a by-product. The Bnchamp reduction is generally mn as a batch process however, it can also be mn as a continuous (48) or semicontinuous process (49). [Pg.262]

In catalytic incineration, there are limitations concerning the effluent streams to be treated. Waste gases with organic compound contents higher than 20% of LET (lower explosion limit) are not suitable, as the heat content released in the oxidation process increases the catalyst bed temperature above 650 °C. This is normally the maximum permissible temperature to which a catalyst bed can be continuously exposed. The problem is solved by dilution-, this method increases the furnace volume and hence the investment and operation costs. Concentrations between 2% and 20% of LET are optimal, The catalytic incinerator is not recommended without prefiltration for waste gases containing particulate matter or liquids which cannot be vaporized. The waste gas must not contain catalyst poisons, such as phosphorus, arsenic, antimony, lead, zinc, mercury, tin, sulfur, or iron oxide.(see Table 1.3.111... [Pg.1258]

We cover each of these types of examples in separate chapters of this book, but there is a clear connection as well. In all of these examples, the main factor that maintains thermodynamic disequilibrium is the living biosphere. Without the biosphere, some abiotic photochemical reactions would proceed, as would reactions associated with volcanism. But without the continuous production of oxygen in photosynthesis, various oxidation processes (e.g., with reduced organic matter at the Earth s surface, reduced sulfur or iron compounds in rocks and sediments) would consume free O2 and move the atmosphere towards thermodynamic equilibrium. The present-day chemical functioning of the planet is thus intimately tied to the biosphere. [Pg.7]

Another way to protect a metal uses an impervious metal oxide layer. This process is known as passivation, hi some cases, passivation is a natural process. Aluminum oxidizes readily in air, but the result of oxidation is a thin protective layer of AI2 O3 through which O2 cannot readily penetrate. Aluminum oxide adheres to the surface of unoxidized aluminum, protecting the metal from further reaction with O2. Passivation is not effective for iron, because iron oxide is porous and does not adhere well to the metal. Rust continually flakes off the surface of the metal, exposing fresh iron to the atmosphere. Alloying iron with nickel or chromium, whose oxides adhere well to metal surfaces, can be used to prevent corrosion. For example, stainless steel contains as much as 17% chromium and 10% nickel, whose oxides adhere to the metal surface and prevent corrosion. [Pg.1408]

Talbot A semi-continuous steelmaking process which combines the Bessemer and Open Hearth processes. Molten pig iron from a Bessemer converter is poured into an Open Hearth furnace containing fresh ore and lime. Impurities in the pig iron oxidize and enter the slag. The process improves the yield of steel and the throughput of the plant. Introduced by B. Talbot at Pencoed, PA, in 1900 and subsequently adopted in Europe. [Pg.265]

A continuous process based on hydrodynamic cavitation can be employed to prepare a wide variety of metal oxides in grain sizes of 1 -10 nm, such as iron oxide, bismuth molybdate, perovskites, platinum-loaded zeolite, and other ceramics and superconductors [170]. The method uses a microfluidiser for mechanically generating hydrodynamic cavitation and the internal pressure of the liquid media is elevated from ambient pressure to between 1000 to 25 000 psi. [Pg.124]

As the rubbing continues, the polyphosphate layer comes into closer contact with water in oil and is hydrolyzed to give a short-chain polyphosphate, e.g., Zn2P207 (Fuller et al., 1998). During the mechanically activated processes (friction coefficient, p > 0.4), a nascent surface is generated, and in the presence of oxygen, an iron oxide is formed. The acid - base reaction between polyphosphate glasses (hard Lewis bases) and the oxides (hard Lewis acids) is... [Pg.7]

Reactions (2) and (3) indicate processes that regenerate Fe2+ in the catalytic cycle. As long as peroxide is available in the system, the iron species continually cycle between Fe2+ and Fe3+, unless additional reactions result in formation of insoluble iron oxides and hydroxides. The rate of formation of hydroxyl radical can be expressed as ... [Pg.173]


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See also in sourсe #XX -- [ Pg.1300 ]




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