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Iron reduction prevention

In contrast, CaM s activation of NO synthesis and substrate-independent NADPH oxidase activity did appear to involve flavin-to-heme electron transfer, because these reactions were not activated in apo-NOS and were blocked in native NOS by agents that prevent heme iron reduction (Abu-Soud et al., 1994a). We conclude that CaM activates neuronal NOS at two points (Fig. 2) electron transfer into the flavins and interdomain electron transfer between the flavins and heme. Activation at each point is associated with an up-regulation of domain-specific catalytic functions. The dual regulation by CaM is unique and represents a new means by which electron transfer can be controlled in a metal-containing flavoprotein. [Pg.210]

PhN02 to form isocyanates 215a7. However a similar activating effect of steel reactor walls was also observed. Ironpalladium black, and ironnitro compound in the active complex. [Pg.147]

Iron(III) chloride and Fe203 promote PdCl2 catalysts containing an heterocyclic base and sometimes M0O3 in the carbonylation of DNT and PhN02 to form isocyanates [161]. However, a similar activating effect of the steel reactor walls was also observed. Iron(III) prevented the reduction of... [Pg.46]

In the above reductions, the amines are present iii the form of salts of the inorganic acid used. In the iron reduction method, however, where only a very small amount of acid is used as a catalyzer, the amines are present mostly as free amines, and for this reason in tlic reduction of fairly volatile substances provision must be made to prevent loss cither of amine or of the initial material. [Pg.69]

The formation of silicon carbide, SiC (carborundum), is prevented by the addition of a little iron as much of the silicon is added to steel to increase its resistance to attack by acids, the presence of a trace of iron does not matter. (Addition of silicon to bronze is found to increase both the strength and the hardness of the bronze.) Silicon is also manufactured by the reaction between silicon tetrachloride and zinc at 1300 K and by the reduction of trichlorosilane with hydrogen. [Pg.166]

The cake produced by the digestion is extracted with cold water and possibly with some diluted acids from the subsequent processes. During the cake dissolution it is necessary to maintain the temperature close to 65°C, the temperature of iron sulfate maximum solubiUty. To prevent the reoxidation of the Fe " ions during processing, a small amount of Ti " is prepared in the system by the Ti reduction. The titanium extract, a solution of titanium oxo-sulfate, iron sulfate, and sulfuric acid, is filtered off. Coagulation agents are usually added to the extract to faciUtate the separation of insoluble sludge. [Pg.8]

Calcium—Silicon. Calcium—silicon and calcium—barium—siUcon are made in the submerged-arc electric furnace by carbon reduction of lime, sihca rock, and barites. Commercial calcium—silicon contains 28—32% calcium, 60—65% siUcon, and 3% iron (max). Barium-bearing alloys contains 16—20% calcium, 9—12% barium, and 53—59% sihcon. Calcium can also be added as an ahoy containing 10—13% calcium, 14—18% barium, 19—21% aluminum, and 38—40% shicon These ahoys are used to deoxidize and degasify steel. They produce complex calcium shicate inclusions that are minimally harm fill to physical properties and prevent the formation of alumina-type inclusions, a principal source of fatigue failure in highly stressed ahoy steels. As a sulfide former, they promote random distribution of sulfides, thereby minimizing chain-type inclusions. In cast iron, they are used as an inoculant. [Pg.541]

The most significant chemical property of zinc is its high reduction potential. Zinc, which is above iron in the electromotive series, displaces iron ions from solution and prevents dissolution of the iron. For this reason, zinc is used extensively in coating steel, eg, by galvanizing and in zinc dust paints, and as a sacrificial anode in protecting pipelines, ship hulls, etc. [Pg.398]

It has been frequently noted that certain lots of iron filings are not satisfactory for the reduction of heptaldehyde to heptyl alcohol in acetic acid solution. E. E. Reld and J. R. Ruhoff have found that the addition of a solution of 20 g. of nickel cliloride hexahydrate in 50 cc. of water immediately after the addition of the aldehyde will cause the reaction to start at once and wiU greatly accelerate the rate of reaction so that it is complete in two hours instead of the usual six to seven hours. The checkers have found this to be the case even with a lot of iron which could not be made to react when reduced in hydrogen. It is also recommended that the reaction mixture be divided between two 12-I. flasks and that 3 1. of water be added to each half immediately at the end of the reaction. This prevents the mixture from setting to a hard mass in case the steam distillation is not carried out at once, and also reduces the amount of foaming. [Pg.91]

Fluid Iron Ore Reduction (FIOR) is a process for reducing ore to iron with a reducing gas in a fluid bed. For thermodynamic efficiency, iron ore reduction requires counter current flow of ore and reducing gas. This is achieved in FIOR in a multiple bed reactor. Precautions are necessary to prevent significant back mixing of solids between beds, since this would destroy counter current staging. [Pg.28]

Red lead (Pb304) is manufactured on the 20000-tonne scale annually and is used primarily as a surface coating to prevent corrosion of iron and steel (check oxidation-reduction potentials). It is also used in the production of leaded glasses and ceramic glazes and. very substantially, as an activator, vulcanizing agent and pigment in natural and artificial rubbers and plastics. [Pg.386]

Charging and tapping emissions are controlled by a variety of evacuation systems and operating practices. Charging hoods, tapside enclosures, and full furnace enclosures are used in the industry to capture these emissions and send them to either the primary hood gas cleaner or a second gas cleaner.1516 Pollution prevention opportunities for the reduction of heavy metals at the BOF are limited as heavy metals are an inherent part of the iron ore material stream, so the higher the iron production, the greater will be the use of the ore. [Pg.52]


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See also in sourсe #XX -- [ Pg.369 , Pg.378 ]




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