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Iron valency

Iron (valence not stated). It is ranked between the K and Cu salts in expl effect in lead plate test when primed with MF (Ref 7)... [Pg.71]

In the electronics industry, for example, the magnetic properties of the iron oxides are used extensively, but the dielectric losses associated with mixed iron valences represent a problem to be minimized by fabrication procedures. [Pg.3]

In the system Mo,Fe3 x04, there is a regular variation with x, from Fe304 to MoFe204, in the lattice parameter (ao), the magnetization (Ms), the Curie temperature (Tc) and the electrical conductivity (a, AH ) apparently substitution of Fe by Mo leads to a mixed iron valence on both sites for 0 < x < 1. It is worth noting that AH varies smoothly with x from a AH < kT for x = 0 in the temperature interval 300 < T < 600 K to 0.027 eV for x = 1.0, where the narrow minority-spin band is maximally perturbed and filled by the introduction of substitutional Mo ... [Pg.41]

Phosphorus-containing iron ores are sometimes used in the steel industry, so an investigation of the Fe-P-O system at 800-1000 C has been made. Some of the new compounds discovered in this work contain mixed iron valencies. [Pg.67]

Not all aspects of biooxidation with the hydrogen peroxide mechanism in the presence of catalase are clear yet. The following mechanism is accepted in the biochemical literature [82], which illustrates formal iron valences in catalase and peroxidase reactions ... [Pg.198]

Figure 6.3 Catalase redox transformation diagram. Compounds II, III and IV represent complexes of the enzyme with H202 and iron valence states, Fe5+, Fe4+ and Fe6+, respectively HXOH is a two-electron donor (reducer) X=0, NH, C=0, H(CH2) CH, where n = 1,2, 3 AH is a single-electron donor (reducer) ROOH is hydroperoxide (R is alkyl or acyl radical) and ROH is alcohol. Figure 6.3 Catalase redox transformation diagram. Compounds II, III and IV represent complexes of the enzyme with H202 and iron valence states, Fe5+, Fe4+ and Fe6+, respectively HXOH is a two-electron donor (reducer) X=0, NH, C=0, H(CH2) CH, where n = 1,2, 3 AH is a single-electron donor (reducer) ROOH is hydroperoxide (R is alkyl or acyl radical) and ROH is alcohol.
Let us turn to the frontier orbitals of the Fe(CO)3 group.37 The three lowest-lying metal orbitals, xy, dX2 and dy2, form a triply degenerate set which accommodates six of the eight iron valence electrons. Only two electrons remain the doubly degenerate dz2 and dx2 y2 orbitals shown below accept one each ... [Pg.224]

Table 8 The electron-transfer series of [FedSd] protein sites and analogs showing core oxidation states and iron valences... Table 8 The electron-transfer series of [FedSd] protein sites and analogs showing core oxidation states and iron valences...
Dyar, M. D. (1985). A review of Mdssbauer data on inorganic glasses the effects of composition on iron valency and coordination. Amer. Mineral. 70, 304-16. [Pg.471]

No change of heme iron valence seems to be involved. [Pg.331]

The iron profile measures the ferrous (Fell), ferric (Felll) and elemental (Fe) iron valencies, as well as soluble, complexed and total iron ... [Pg.45]

When iron is added to a food the environment is going to affect the valence state as has been discussed previously. One of the parameters which might maintain a particular valence state in the face of adverse environmental conditions, such as pH or redox potential, is the stability of its complex. Therefore, either the Fe+ or Fe+3 form might be maintained if one formed a complex with a greater thermodynamic stability than the other as discussed previously. Therefore, it would seem that the importance of the thermodynamic stability constant should not be discounted because it could have a great deal of relevance with respect to solubility and maintenance of a specific iron valence within a given food system. [Pg.76]

Raeburn SP, Kerrick DM, Gorshe R, Barth G (1993) (Quantitative microbeam determination of iron valence by XPS and XES—revisited. EOS Trans Am Geophys Union 74 161 Rancouit DG (1989) Accurate site populations from Mossbauer spectroscopy. Nucl Instr Meth Phys Res B44 199-210... [Pg.347]

Lytle FW, Pingitore NE Jr (2002) Iron valence in the hydration layer of obsidian characterization by X-ray absorption spectroscopy. Microchemical J 71 185-191... [Pg.89]

The electronic structure of the cubane clusters can be understood only on the basis of pairwise iron valence delocalization of solely high-spin ferrous (5 = 2) and ferric (5 = 5/2) ions. The four (or three) iron of the cluster, numbered 1-4, exhibit pairwise valence delocalization that results in a near ferromagnetic cou-phng for the pairs, 5a = 5i -I- 52 and 5b = 5a + 54, with the net cluster spin, resulting from antiferromagnetic coupling for the net spins for the two pairs of... [Pg.354]

For getting specific type of data to unfold the needed information the details of techniques described in this chapter helps to understand and choose a particular technique. For instance x-ray diffraction for internal structure analysis, XRF for elemental composition and XRD for crystal structure analysis, Mossbauer techniques for identification of iron valency state, thermal interaction analysis for decomposition/intemal structure change. [Pg.106]

Schematic feature of the rapid spin equilibrium in the Fe" 03S3 site and its effect on the iron valence fluctuation in (n-C4H9)4N [Fe"Fe" (mto)3]. (Reproduced from Ref. 33 with permission of MDPI Publishing.)... Schematic feature of the rapid spin equilibrium in the Fe" 03S3 site and its effect on the iron valence fluctuation in (n-C4H9)4N [Fe"Fe" (mto)3]. (Reproduced from Ref. 33 with permission of MDPI Publishing.)...
Another well-known mineral is pseudobrookite, which consists of a complete solid solution series between ferrous FeTi205 and ferric Fe2Ti05. Also in this case, the Mossbauer spectra reveal iron species that vary from Fe " over mixed valences to Fe. However, the structure contains two different sites (8f and 4c) where iron can be present, resulting in two doublets for each iron valence. The hyperfine parameters according to Guo et al. [Ill] are summarized in Table 3.5. [Pg.115]

Effective resorption is dependent not only on the iron valence, but can be enhanced or diminished in the presence of certain food components. [Pg.435]


See other pages where Iron valency is mentioned: [Pg.458]    [Pg.11]    [Pg.129]    [Pg.321]    [Pg.3774]    [Pg.740]    [Pg.348]    [Pg.27]    [Pg.46]    [Pg.72]    [Pg.80]    [Pg.11]    [Pg.374]    [Pg.223]    [Pg.740]    [Pg.336]    [Pg.106]    [Pg.106]    [Pg.135]    [Pg.275]    [Pg.1466]    [Pg.270]    [Pg.175]    [Pg.276]    [Pg.434]    [Pg.212]    [Pg.309]    [Pg.85]   
See also in sourсe #XX -- [ Pg.80 , Pg.131 , Pg.166 ]




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High valence iron compounds

Iron complexes 18 valence electron rule

Iron complexes 19 valence electrons

Iron mixed valence compounds

Iron porphyrins valence electronics

Iron-sulfur proteins valence delocalization

Iron-sulfur proteins, valence

Iron-sulfur proteins, valence electrons

Mixed-valence iron pairs

Spin and Valence States of Iron in Silicate Perovskite

Spin and Valence States of Iron in Silicate Postperovskite

Valence electron counts, iron clusters

Valence of iron

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