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Fused Iron Oxide

The principal limitations of ESCA include the inability to detect elements present at trace concentrations within the analytical volume, and insufficient lateral resolution to characterize single micrometer-sized particles. The inability to characterize trace species is illustrated in Figure 10 for a sample of coal fly ash particles (11). The fly ash results from the noncombustible mineral components of the coal and consists largely of fused iron oxides and aluminosilicates (42). In addition, most elements are present in at least trace concentrations (22, 42), and many of these elements are highly enriched in the surface region of the particles (evidence for this will be discussed in the next section). However, the ESCA spectrum acquired over several hours of counting time indicates only the presence of detectable surface S and Ca in addition to the fly ash matrix constituents. [Pg.146]

The reduced fused iron oxide for ammonia synthesis is a perfect example illustrating in its textural and structural complexity the merit of this preparation strategy which allows to create a metastable porous form of the element iron. The necessary kinetic stabilization of the mctastable solid is achieved by the exsolution of irreducible oxide phases of structural promoters. Some of them precipitate during solidification. [Pg.20]

A number of substances show considerable activity as ammonia catalysts. Fe, Os, and Re and nitrides of Mo, W, and U are the best known. Iron in the form of promoted iron catalysts is by far the most important, maybe the only type in industrial use, and except for a few comparisons, iron catalysts will be the only type dealt with in this paper. Furthermore, the discussion will be limited to the type of catalysts made by fusing iron oxides together with the promoter components and subsequently reducing the catalysts. This limitation is not too important, since this type of catalyst is the one most widely used and also the type on which most fundamental work has been done. [Pg.2]

Most of the world s ammonia supply is manufactured by the addition of hydrogen to nitrogen over an iron-based catalyst at elevated temperatures and pressures. A typical catalyst is prepared by fusing iron oxides with a small amount of potassium and aluminum oxides as promoters and reducing the granulated oxide mixture with synthesis gas to reduce the iron oxide to free iron. [Pg.450]

Fused iron oxide with silica, magnesia, potash promoters. Acetylene hydrogenation in depropanizer overhead streams. [Pg.103]

Despite the problems at Sheffield, the Atmospheric Nitrogen Corporation, a subsidiary of the General Chemical Company, had built and operated a second plant with the same design at Syracuse, New York by 1921.The original capacity was 15 tonnes per day anunonia but it was later increased to 40 totmes per day. This plant eventually used a fused iron oxide catalyst, promoted with alumina and potash, developed at the Fixed Nitrogen Research Laboratory by A T Larson. It had first test a catalyst developed by de Jahn of the General Chemical Company. [Pg.402]

Mixed zircon, coke, iron oxide, and lime reduced together produce zirconium ferrosiUcon [71503-20-3] 15 wt % Zr, which is an alloy agent. Fused zirconia [1314-23-4] has been made from zircon but baddeleyite is now the preferred feed for the production of fused zirconia and fused alumina—zirconia by electric-arc-fumace processing. [Pg.429]

Iron oxides are stable pigments iasoluble ia most solvents but usually soluble ia hydrochloric acid. Those not soluble ia HCl can be fused with potassium hydrogen sulfate, KHSO, and then dissolved ia water. [Pg.452]

The weld was riddled with mildly undercut, gaping pits. Attack was confined to fused and heat-affected zones, with a pronounced lateral or circumferential propagation (as in Fig. 6.10). The resulting perforation at the external surface was quite small. Pits were filled with deposits, friable oxides, and other corrosion products. Black plugs embedded in material filling the gaping pit contained high concentrations of iron sulfide. Bulk deposits contained about 90% iron oxide. Carbonaceous material was not detected. [Pg.147]

The behaviour of iridium is closely analogous to that of rhodium its corrosion diagram is very similar and it is, with rhodium, one of the least corrodible of metals. It is unattacked by alkalis, acids or oxidising agents in aqueous solution, although a fused mixture of caustic potash and potassium nitrate will attack it. The metal has an excellent resistance to fused lead oxide, silicates, molten copper and iron at temperatures up to 1 500°C. Additions of iridium to platinum considerably raise the corrosion resistance of the latter to a very wide range of reagents. [Pg.931]

Silica Refractories. This type consists mainly of silica in three crystalline forms cristobalite [1446446-1]> tridymite [1546-32-3]> and quartz [14808-60-7]. Quartzite sands and silica gravels are the main raw materials, although lime and iron oxides are added to increase the mineralization of the tridymite and cristobalite. Uses include roof linings, refractories for coke ovens, coreless induction foundry furnaces, and fused-silica technical ceramic products. Consumption of silica refractories has declined dramatically since the 1960s as a result of the changes in the steel industry. [Pg.37]

Other reported syntheses include the Reimer-Tiemann reaction, in which carbon tetrachloride is condensed with phenol in the presence of potassium hydroxide. A mixture of the ortho- and para-isomers is obtained the para-isomer predominates. -Hydroxybenzoic acid can be synthesized from phenol, carbon monoxide, and an alkali carbonate (52). It can also be obtained by heating alkali salts of -cresol at high temperatures (260—270°C) over metallic oxides, eg, lead dioxide, manganese dioxide, iron oxide, or copper oxide, or with mixed alkali and a copper catalyst (53). Heating potassium salicylate at 240°C for 1—1.5 h results in a 70—80% yield of -hydroxybenzoic acid (54). When the dipotassium salt of salicylic acid is heated in an atmosphere of carbon dioxide, an almost complete conversion to -hydroxybenzoic acid results. They>-aminobenzoic acid can be converted to the diazo acid with nitrous acid followed by hydrolysis. Finally, the sulfo- and halogenobenzoic acids can be fused with alkali. [Pg.292]

We can start, as did the ancient craftsmen, with the fusion of the iron oxide, FeO, with silica, SiO . The phase diagram for those binary mixtures show that whereas Si02 fuses at about 1713 C and FeO at 13 9 C, mixtures containing between 20 and 40 weight percent FeO fuse below 1250 C. Complexing with additions of another iron oxide, Fe203, in amounts of up to 10%, can lower the fusion temperature to about 1150 C. [Pg.262]

Two substrate materials were used for most of the measurements. They were chosen as representative of two types of environmental material found in actual fallout. The first was a clay loam occurring in the Berkeley Hills, Calif. This is a more-or-less typical example of a silicate soil found in extensive areas in the temperate zones. The second material used was a calcium ferrite. This material has been observed in fallout resulting from nuclear explosions at the Pacific Proving Grounds where large amounts of calcium oxide, derived from the coral sand, and iron oxide, derived from towers, barges, or other structures, have been fused together. [Pg.44]


See other pages where Fused Iron Oxide is mentioned: [Pg.660]    [Pg.981]    [Pg.982]    [Pg.106]    [Pg.403]    [Pg.660]    [Pg.981]    [Pg.982]    [Pg.106]    [Pg.403]    [Pg.729]    [Pg.10]    [Pg.11]    [Pg.319]    [Pg.284]    [Pg.437]    [Pg.164]    [Pg.52]    [Pg.37]    [Pg.292]    [Pg.164]    [Pg.324]    [Pg.199]    [Pg.198]    [Pg.116]    [Pg.137]    [Pg.916]    [Pg.230]    [Pg.629]    [Pg.173]    [Pg.440]    [Pg.433]    [Pg.591]    [Pg.324]    [Pg.284]    [Pg.164]    [Pg.437]    [Pg.159]    [Pg.532]    [Pg.254]    [Pg.333]   


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