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Iron solid phases

This study detects the defect of the void and the exfoliation in the solid phase diffusion bonding interface of ductile cast iron and stainless steel with a nickel insert metal using ultrrasonic testing method, and examine the influence of mutual interference of the reflectional wave both the defect and the interface. [Pg.833]

Saito described a quantitative spectrophotometric procedure for iron based on a solid-phase extraction using bathophenanthroline in a poly(vinyl chloride) membrane. ... [Pg.452]

The iron-carbon solid alloy which results from the solidification of non blastfurnace metal is saturated with carbon at the metal-slag temperature of about 2000 K, which is subsequendy refined by the oxidation of carbon to produce steel containing less than 1 wt% carbon, die level depending on the application. The first solid phases to separate from liquid steel at the eutectic temperature, 1408 K, are the (f.c.c) y-phase Austenite together with cementite, Fe3C, which has an orthorhombic sttiicture, and not die dieniiodynamically stable carbon phase which is to be expected from die equilibrium diagram. Cementite is thermodynamically unstable with respect to decomposition to h on and carbon from room temperature up to 1130 K... [Pg.184]

The equilibrium constitution of a one-component system is fixed by the variables p and T and so the equilibrium phases can be shown on a diagram with p and T axes. The one shown in Fig. A1.6 has only one solid phase. Some, like ice, or iron, have several. [Pg.331]

Thus the diagram shows the solid phases of iron, the activities of metal ions and the pressures of hydrogen and oxygen gas that are at equilibrium at any given potential and pH when pure iron reacts with pure water. [Pg.67]

Fig. 7.2 Fe-O phase diagram showing the principal solid phases stable on iron and wide stoichiometry limits of FeO (after White )... Fig. 7.2 Fe-O phase diagram showing the principal solid phases stable on iron and wide stoichiometry limits of FeO (after White )...
Over the years, Pourbaix and his co-workers in the CEBELCOR Institute, founded under his direction, extended these diagrams by including lines for metastable compounds. Figure 7.66 illustrates such a presentation for the Fe-O system over the temperature range 830-2200 K. Pourbaix used these diagrams as a basis for a discussion of the stability of metallic iron (solid, liquid and vapour phases), the oxides of iron as a function of oxygen pressure and temperature from which he explained the protection of iron at high temperature by immunity and passivation. He also pointed out the... [Pg.1111]

From Fig.2 (a), A solid phase transformation fiom hematite, Fc203 to magnetite, Fe304, is observed, indicating that the active sites of the catalj are related to Fc304. Suzuki et. al also found that Fe304 plays an important role in the formation of active centers by a redox mechanism [6]. It is also observed that the hematite itself relates to the formation of benzene at the initial periods, but no obvious iron carbide peaks are found on the tested Li-Fe/CNF, formation of which is considered as one of the itsisons for catalyst deactivation [3,6]. [Pg.744]

This method was used, for example, for the solid-phase immunoassay of thyroxine (affinity chromatography). Various activation methods (CDI, periodate, and cyanogen bromide procedures) were compared with each other for coupling antibodies to magnetizable cellulose/iron oxide solid-phase particles. 211]... [Pg.144]

Primary copper processing results in air emissions, process wastes, and other solid-phase wastes. Particulate matter and sulfur dioxide are the principal air contaminants emitted by primary copper smelters. Copper and iron oxides are the primary constituents of the particulate matter, but other oxides, such as arsenic, antimony, cadmium, lead, mercury, and zinc, may also be present, with metallic sulfates and sulfuric acid mist. Single-stage electrostatic precipitators are widely used in the primary copper industry to control these particulate emissions. Sulfur oxides contained in the off-gases are collected, filtered, and made into sulfuric acid. [Pg.84]

Dang et al. (1994) observed that the experimentally determined solubility lines for Zn2+ in 14 soil solutions from southern Queensland with soil pH from 7.45-8.98 and 0.08-2.07% CaC03 were not undersaturated with respect to the solubility of any known mineral form of Zn. Therefore, they suggested that Zn2+ activity was mainly controlled by adsorption-desorption reactions in these soils. Similar observation on solubility of Cr(VI) in arid soils was reported by Rai et al. (1989). In the absence of a solubility controlling solid phase, Cr(VI) aqueous concentrations under slightly alkaline conditions may be primarily controlled by adsorption/desorption reactions (Rai et al., 1989). Chromuim(VI) is adsorbed by iron and aluminum oxides, and kaolinite and its adsorption decreases with increasing pH. [Pg.102]

Iron and Mn oxides are two of the most important solid-phase components controlling distribution and availability of trace elements in arid... [Pg.136]

Schneider, 1984 Schneider and Schwyn, 1987 Schneider, 1988 Cornell et al., 1989). Perchlorate solutions that contain the dinuclear Fe2(OH)24+ to about 10 % of the total iron concentration can be kept unchanged for several weeks. This is by no means trivial, because it was recognized many years ago that solutions containing Fe2(OH)24+ to a significant degree are supersaturated with respect to solid phases such as FeO(OH) (Biedermann and Schindler, 1957). The low molecular species interact to produce species with a higher nuclearity (equation 7) ... [Pg.50]


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See also in sourсe #XX -- [ Pg.65 ]




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Solid phases of iron

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