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Oxidation iron nitrate

Eisenozyd, n. iron oxide, specif, ferric oxide, iron(Ul) oxide. — salpetersaures —, ferric nitrate, iron(III) nitrate (and so for other salts). [Pg.125]

A ground mixture of iron(III) nitrate and HZSM-5 zeolite, termed zeofen , has also been used both, in dichloromethane solution and in solid state under MW irradiation conditions [101]. It has been suggested that the zeolite aids the reproducibility of the reaction but any other aluminosilicate support would probably be equally effective. Recent studies point out attractive alternatives that do not employ any of the solid supports in such oxidations with nitrate salts [102]. [Pg.197]

Geochemists (e.g., Thorstenson et al., 1979 Thorstenson, 1984) have long recognized that at low temperature many redox reactions are unlikely to achieve equilibrium, and that the meaning of Eh measurements is problematic. Lindberg and Runnells (1984) demonstrated the generality of the problem. They compiled from the watstore database more than 600 water analyses that provided at least two measures of oxidation state. The measures included Eh, dissolved oxygen content, concentrations of dissolved sulfate and sulfide, ferric and ferrous iron, nitrate and ammonia, and so on. [Pg.103]

Ammonium nitrate Ammonium perchlorate Barium chlorate (hydrate) Barium chromate Barium nitrate Barium peroxide Iron oxide Iron oxide Lead chromate Lead oxide (red lead) Lead peroxide Potassium chlorate Potassium nitrate Potassium perchlorate Sodium nitrate Strontium nitrate... [Pg.20]

Ferric Nitrate (Iron Nitrate), Fe(N0s)3.9H30 mw 404.02, It viol monocl delq crysts, mp 47°, dec at 100° v sol in w ale. Can be prepd by the action of coned nitric acid on scrap iron or on iron oxide, followed by crystn. It is a strong oxidizing agent and is considered to be dangerous as a fire hazard. Used in analytical chemistry... [Pg.397]

During the course of studying the effect of crystallite sizes, attempts were made to produce very small unsupported iron oxide powders by lowering the calcination temperature of the iron hydroxyl gel that was precipitated from iron nitrate with ammonium hydroxide. However, catalysts calcined below 300°C still contain hydroxide, and they show high selectivity in butadiene production. For this reason, two catalysts, calcined at 250°C and 300°C, respectively, were studied in more detail. [Pg.193]

A powder which burns with a green flame is obtained by the addition of nitrate of baryta to chlorate of potash, nitrate of potash, acetate of copper. A white flame is made by the addition of sulfide of antimony, sulfide of arsenic, camphor. Red by the mixture of lampblack, coal, bone ash, mineral oxide of iron, nitrate of strontia, pumice stone, mica, oxide of cobalt. Blue with ivory, bismuth, alum, zinc, copper sulfate purified of its sea water [sic]. Yellow by amber, carbonate of soda, sulfate of soda, cinnabar. It is necessary in order to make the colors come out well to animate the combustion by adding chlorate of potash.15... [Pg.61]

It has been demonstrated that BTEX compounds can readily be oxidized using nitrate as an electron acceptor [29,40-42]. With only a few exceptions (for instance, ethylbenzene has not been demonstrated to degrade under sulfate-reducing conditions), BTEX oxidation using sulfate, carbon dioxide, ferric iron,... [Pg.45]

Nitric acid tends to oxidize iron(II) ions hence it is advisable to maintain the nitrate-ion concentration as low as possible and to keep the solution cold. [Pg.458]

Determine the spray roasted particle diameter resulting from the Rayleigh breakup of a jet 0.1 mm in diameter operating on a 0.01 molar doped iron nitrate solution of Ni-Al—Ga spinel ferrite (i.e., MFe204M = Nio 5-AI0 3—Gao ). Assume that the roasting conditions are sufficient to thermally decompose the hydrated metal nitrates that result from spray drying to their respective individual oxides. [Pg.353]

Passivation Inhibitors. Examples of passivators (anodic inhibitors) include chromate, nitrite, molybdate, and orthophosphate. AH are oxidizers and promote passivation by increasing the electrical potential of the iron. Chromate and nitrite do not require oxygen, and thus, can he the most effective. Chromate is an excellent aqueous corrosion inhibitor, particularly from a cost perspective. However, owing to health and environmental concerns, use of chromate has decreased significandy and will probably he outlawed soon. Nitrite is also an effective inhibitor, but in open systems it tends to be oxidized to nitrate. [Pg.269]


See other pages where Oxidation iron nitrate is mentioned: [Pg.458]    [Pg.151]    [Pg.278]    [Pg.102]    [Pg.55]    [Pg.121]    [Pg.141]    [Pg.368]    [Pg.200]    [Pg.72]    [Pg.429]    [Pg.270]    [Pg.347]    [Pg.204]    [Pg.376]    [Pg.111]    [Pg.149]    [Pg.213]    [Pg.213]    [Pg.215]    [Pg.164]    [Pg.314]    [Pg.126]    [Pg.134]    [Pg.72]    [Pg.371]    [Pg.275]    [Pg.399]    [Pg.114]    [Pg.44]    [Pg.1000]    [Pg.868]    [Pg.278]    [Pg.3724]    [Pg.407]   
See also in sourсe #XX -- [ Pg.270 ]




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