Ferrous, definition

Standardized techniques atomic absorption (AAA) and photometric (FMA) of the analysis and designed by us a technique X-Ray fluorescence of the analysis (XRF) for metals definition in air of cities and the working areas of plants to production of non-ferrous metals are applied. The samples of aerosols were collected on cellulose (AFA-HA) and perchlorovinyl (AFA-VP and FPP) filters (Russia). The techniques AAA and FMA include a stage of an acid-temperature ashing of a loaded filter or selective extraction of defined elements from filter by approaching dissolvent. At XRF loaded filters were specimens. 

Two other methods worth discussing are wet air oxidation and regeneration by steam. Wet oxidation may be defined as a process in which a substance in aqueous solution or suspension is oxidized by oxygen transferred from a gas phase in intimate contact with the liquid phase. The substance may be organic or inorganic in nature. In this broad definition, both the well known oxidation of ferrous salts to ferric salts by exposure of a solution to air at room temperature and the adsorption of oxygen by alkaline pyrogallol in the classical Orsat gas analysis would be considered wet oxidations. 

Martensitic phase transformations are discussed for the last hundred years without loss of actuality. A concise definition of these structural phase transformations has been given by G.B. Olson stating that martensite is a diffusionless, lattice distortive, shear dominant transformation by nucleation and growth . In this work we present ab initio zero temperature calculations for two model systems, FeaNi and CuZn close in concentration to the martensitic region. Iron-nickel is a typical representative of the ferrous alloys with fee bet transition whereas the copper-zink alloy undergoes a transformation from the open to close packed structure. ... 

Characteristics and implementation of the treatments depend on the expected results and on the properties of the material considered a variety of processes are employed. In ferrous alloys, in steels, a eutectoid transformation plays a prominent role, and aspects described by time-temperature-transformation diagrams and martensite formation are of relevant interest. See a short presentation of these points in 5.10.4.5. Titanium alloys are an example of the formation of structures in which two phases may be present in comparable quantities. A few remarks about a and (3 Ti alloys and the relevant heat treatments have been made in 5.6.4.1.1. More generally, for the various metals, the existence of different crystal forms, their transformation temperatures, and the extension of solid-solution ranges with other metals are preliminary points in the definition of convenient heat treatments and of their effects. In the evaluation and planning of the treatments, due consideration must be given to the heating and/or cooling rate and to the diffusion processes (in pure metals and in alloys). 

For the electron transfer of hydrated redox particles (the outer-sphere electron transfer), the electrode acts merely as a source or sink of electrons transferring across the compact double layer so that the nature of the electrode hardly affects the reaction kinetics this lack of influence by the electrode has been observed for the ferric-ferrous redox reaction. On the other hand, the electron transfer of adsorbed redox particles (the inner-sphere electron transfer) is affected by the state of adsorption so that the nature of the electrode exerts a definite influence on the reaction kinetics, as has been observed with the hydrogen electrode reaction where the reaction rate depends on the property of electrode. 

One of these, electron transfer, actually occurs in the ideal definitional sense. It applies to the few overworked redox reactions where there is no adsorbed intermediate. The ion in a cathodic transfer is located in the interfacial region and receives an electron (ferric becomes ferrous) without the nucleus of the ion moving. Later (perhaps as much as 10-9 s later), a rearrangement of the hydration sheath completes itself because that for the newly produced ferrous ion in equilibrium differs (in equilibrium) substantially from that for the ferric. Now (even in the electron transfer case) the ion moves, but the definition remains intact because it moves after electron transfer. The amounts of such small movements (changes in the ion-solvent distance for Fe2+ and Fe3+ ions in equilibrium) are now known from EXAFS measurements. 

SALTS OF IKON.—It has been shown that iron is susceptible of two definite degrees of oxidisation, forming a protoxide—FeO—and a sesquioxlde — Fea Oa. Both those oxides are salifiable, giving rise to ferrous and feme Baits. The most important is the native protocarbonate, which constitutes the principal source of British iron, and has, therefore, been fully described in treating of the ores of this metal. 

By definition these are the materials whose physical properties and cost performance ratios allow them to compete with and replace traditionally accepted ferrous and non-ferrous metals as well as other mechanically functionable design materials. 

Edmondson et al (1971), who studied the enrichment of whole milk with iron, found that ferrous compounds normally caused a definite oxidized flavor when added before pasteurization. Aeration before addition of the iron reduced the off-flavor. The authors recommended the addition of ferric ammonium citrate followed by pasteurization at 81 °C. Kurtz et al. (1973) reported that iron salts can be added in amounts equivalent to 20 mg iron per liter of skim milk with no adverse flavor effects when iron-fortified dry milk is reconstituted to skim milk or used in the preparation of 2% milk. Hegenauer et al. (1979A) reported that emulsification of milk fat prior to fortification greatly reduced lipid peroxidation by all metal complexes. These researchers (Hegenauer et al. 1979B) concluded that chelated iron and copper should be added after homogenization but before pasteurization by a high-temperature-short-time process. 

Ferric Oxide.—The filtrate from the preceding determination is made up, together with the wash water, to a definite volume (e.g., 250 c.c.) and an aliquot part of it (50 or 100 c.c.) precipitated with ammonia in presence of ammonium chloride the predpitate is collected on a filter and washed. If alumina is present only in negligible quantity, the weight of the caldned predpitate gives the ferric oxide. In the contrary case, the washed and still wet predpitate is dissolved in dilute sulphuric acid and the solution made up to 100 c.c. with water 10 c.c. of this solution are reduced with zinc and the ferrous iron titrated with permanganate (see Vol. I, Limestones and Marls, p. 142). 

It is established, that during the carbonization of systems HC- salt of metal of ferrous subgroup the reducing of the salts to the free metals take place. These highly disperse metals catalyze (at definite THT) the processes of carbon structuring with formation of different phases of ordered carbon. On literary data... 

Reduction. The nitro compound is reduced by means of a concentrated solution of sodium hydrosulfide, NaSH, the preparation of which was described on page 113. A test is made in the following way to determine how much of the reducing agent is required 25 cc. of the filtered solution of the nitro compound is pipetted into a 750-cc. Erlen-meyer flask, diluted with 350 cc. hot water, and neutralized with soda to the point where the red coloration, which is formed, just persists. A sodium hydrosulfide solution, prepared by diluting 10 cc. of the concentrated solution to 100 cc., is then added, at 60-70°, from a burette until the color of the solution turns to a piure blue. Additional 1-cc. portions of the hydrosulfide solution are added until a definite blackening is obtained when the colorless spot on filter paper, formed by a salted-out test sample, is treated with ferrous sulfate. From the amount of hydrosulfide used in the test determination, the amount required for the total volume of the nitro solution is calculated. 

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