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Manganese oxide, reduction

Ehrlich, H.L., Manganese oxide reduction as a form of anaerobic respiration, Geomicrobiol. J., 5, 423-429, 1987... [Pg.853]

Oxidation of arsenic-bearing pyrite with adsorption onto iron oxides and/or other metal (oxy)(hydr)oxides Nitrate reduction by pyrite oxidation (note that Appelo and Postma, 1999 referred to pure rather than arsenian pyrite) Manganese oxide reduction and release of sorbed arsenic Fe(lll) reduction on oxide surfaces changes net charge leading to arsenic desorption Iron oxide reductive dissolution and release of sorbed arsenic catalyzed by NOM degradation... [Pg.312]

Figure 8.2. Rates of manganese oxide reductive dissolution by 1.00 x 10 4 M oxalate as a function of pH. Reactions were performed in 5.0 x 10 2 M NaCl using either acetate (O) or constant -Pco2 (P) buffers. ([MnOx]0 is 4.81 x 10 5 M.) Numerical values are apparent reaction orders with respect to [H+], [From Stone (1987a), with permission.]... Figure 8.2. Rates of manganese oxide reductive dissolution by 1.00 x 10 4 M oxalate as a function of pH. Reactions were performed in 5.0 x 10 2 M NaCl using either acetate (O) or constant -Pco2 (P) buffers. ([MnOx]0 is 4.81 x 10 5 M.) Numerical values are apparent reaction orders with respect to [H+], [From Stone (1987a), with permission.]...
Key words low-grade manganese oxides, reduction roasting, biomass charcoal... [Pg.317]

First-Row Transition Elements Scandium to Manganese—Oxidation-reduction reactions are commonly encountered with transition metal compounds of Sc, Ti, V, Cr, and Mn. Two common types of oxidizing agents are the dichromates and permanganates. In aqueous solution, dichromate ion is in equilibrium with chromate ion. [Pg.1122]

Manganese is the third most abundant transition metal, and is widely distributed in the earth s crust. The most important ore is pyrolusite, manganese(IV) oxide. Reduction of this ore by heating with aluminium gives an explosive reaction, and the oxide Mn304 must be used to obtain the metal. The latter is purified by distillation in vacuo just above its melting point (1517 K) the pure metal can also he obtained by electrolysis of aqueous manganese(II) sulphate. [Pg.384]

The dissolution of carbon in molten iron in the lower part of the furnace, leads to the reduction of manganese oxide (eq. 15) and some sihea (eq. 14), both in the slag, whereby the subsequent dissolution of these metals occurs in the molten iron. [Pg.166]

Benzylacetophenone has been prepared by the reduction of benzalacetophenone with zinc and acetic acid1 and catalytic-ally with palladium and hydrogen 2 by the reduction of /3-duplo-benzylidene acetophenone monosulfide 3 by the oxidation of the corresponding car bind with chromic acid 4 by the hydrolysis of ethyl benzyl benzoylacetate 5 from acetophenone and benzyl chloride by the action of sodamide 6 and from benzoic and hydrocinnamic adds using as catalysts manganese oxide 7 and ferric oxide.8... [Pg.37]

Metal cycles Iron and manganese oxidation and reduction Iron bacteria and manganese bacteria... [Pg.49]

In addition to effects on the concentration of anions, the redox potential can affect the oxidation state and solubility of the metal ion directly. The most important examples of this are the dissolution of iron and manganese under reducing conditions. The oxidized forms of these elements (Fe(III) and Mn(IV)) form very insoluble oxides and hydroxides, while the reduced forms (Fe(II) and Mn(II)) are orders of magnitude more soluble (in the absence of S( — II)). The oxidation or reduction of the metals, which can occur fairly rapidly at oxic-anoxic interfaces, has an important "domino" effect on the distribution of many other metals in the system due to the importance of iron and manganese oxides in adsorption reactions. In an interesting example of this, it has been suggested that arsenate accumulates in the upper, oxidized layers of some sediments by diffusion of As(III), Fe(II), and Mn(II) from the deeper, reduced zones. In the aerobic zone, the cations are oxidized by oxygen, and precipitate. The solids can then oxidize, as As(III) to As(V), which is subsequently immobilized by sorption onto other Fe or Mn oxyhydroxide particles (Takamatsu et al, 1985). [Pg.390]

The reduction of manganese oxides by aluminum has been used for the production of manganese metal. The process is also a classic example to illustrate thermal energy management in a typical aluminothermic reduction process. [Pg.390]

Other metal oxide catalysts studied for the SCR-NH3 reaction include iron, copper, chromium and manganese oxides supported on various oxides, introduced into zeolite cavities or added to pillared-type clays. Copper catalysts and copper-nickel catalysts, in particular, show some advantages when NO—N02 mixtures are present in the feed and S02 is absent [31b], such as in the case of nitric acid plant tail emissions. The mechanism of NO reduction over copper- and manganese-based catalysts is different from that over vanadia—titania based catalysts. Scheme 1.1 reports the proposed mechanism of SCR-NH3 over Cu-alumina catalysts [31b],... [Pg.13]

Fuel cell applications Manganese dioxide as a new cathode catalyst in microbial fuel cells [118] OMS-2 catalysts in proton exchange membrane fuel cell applications [119] An improved cathode for alkaline fuel cells [120] Nanostructured manganese oxide as a cathodic catalyst for enhanced oxygen reduction in a microbial fuel cell [121] Carbon-supported tetragonal MnOOH catalysts for oxygen reduction reaction in alkaline media [122]... [Pg.228]

Soil pH affects the transformation of Cr between Cr(III) and Cr(VI) in soils. Since Cr(VI) has greater bioavailability and mobility in soils than Cr(III), which is strongly bound by soil solid matrix (Han and Banin, 1997). Cr(III) can be oxidized by soil manganese oxides into Cr(VI), while Cr(VI) can be reduced by organic matter, Fe(II) and microorganisms in soils. Reduction of Cr(VI) has been found to occur much slower in alkaline soils compared to acid soils (Cary et al., 1997). [Pg.239]

In well-aerated soil, it is expected that all species will be in their highest oxidation states. However, this does not happen for reasons elucidated in previous chapters. In well-aerated soil, both ferrous and ferric iron can exist along with elemental iron.3 Zinc, copper, and especially manganese can apparently exist in a mixture of oxidation states simultaneously in soil. Add to this a multitude of organic species that are also capable of oxidation-reduction reactions and the result is truly a complex voltammetric system [12,13],... [Pg.204]


See other pages where Manganese oxide, reduction is mentioned: [Pg.817]    [Pg.227]    [Pg.316]    [Pg.210]    [Pg.3917]    [Pg.122]    [Pg.76]    [Pg.167]    [Pg.817]    [Pg.227]    [Pg.316]    [Pg.210]    [Pg.3917]    [Pg.122]    [Pg.76]    [Pg.167]    [Pg.250]    [Pg.379]    [Pg.490]    [Pg.494]    [Pg.505]    [Pg.166]    [Pg.107]    [Pg.615]    [Pg.281]    [Pg.34]    [Pg.214]    [Pg.518]    [Pg.367]    [Pg.389]    [Pg.390]    [Pg.710]    [Pg.816]    [Pg.220]    [Pg.240]    [Pg.69]    [Pg.171]    [Pg.166]    [Pg.382]    [Pg.1483]    [Pg.223]    [Pg.213]   
See also in sourсe #XX -- [ Pg.344 ]

See also in sourсe #XX -- [ Pg.344 ]

See also in sourсe #XX -- [ Pg.483 ]

See also in sourсe #XX -- [ Pg.241 , Pg.249 , Pg.254 , Pg.256 , Pg.260 ]




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Manganese oxidation

Manganese oxides, reductive

Manganese-oxidizing

Oxidants manganese

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