Reactions direct oxide reduction

The use of this direct oxide reduction process is replacing fluoride reduction as it eliminates neutron exposure to operating personnel (alpha particles from plutonium decay have sufficient energy to eject neutrons from fluorine by the a,n reaction) and eliminates reduction residues which require subsequent recovery. 

The reaction is carried out under an inert atmosphere in an open crucible at approximately 830°C. Figure 1 shows typical equipment used for direct oxide reduction. Vitrified magnesium oxide ceramic is commonly used as a container material, but tungsten and tantalum can also be used(3). If the latter are used, CaF2 is added to lower the temperature needed to liquify... 

Although the exact chemical mechanism for the direct oxide reduction reaction has not yet been fully characterized, it has been well established that the reaction goes to completion when excess calcium is present, sufficient CaCl2 is available to dissolve the CaO produced, and adequate stirring is used. As calcium metal is soluble to about 1 wt% in CaC12 at 835°C, excess Ca insures that the reaction is driven to completion by mass-action effects. 

Direct Oxide Reduction. In DOR, plutonia is reduced with calcium metal to form plutonium metal and calcium oxide.2 3 The reaction takes place in a CaCl2 solvent which dissolves the calcium oxide and allows the plutonium metal to coalesce in the bottom of the crucible. 

Direct Oxide Reduction. In DOR, calcium chloride is used as a solvent to dissolve the calcium oxide in the reaction ... 

Analytical methods based upon oxidation/reduction reactions include oxidation/reduction titrimetry, potentiometry, coulometry, electrogravimetry and voltammetry. Faradaic oxidation/reduction equilibria are conveniently studied by measuring the potentials of electrochemical cells in which the two half-reactions making up the equilibrium are participants. Electrochemical cells, which are galvanic or electrolytic, reversible or irreversible, consist of two conductors called electrodes, each of which is immersed in an electrolyte solution. In most of the cells, the two electrodes are different and must be separated (by a salt bridge) to avoid direct reaction between the reactants. 

It should be noted that all terms concerning the electrons in the metals as well as those connected with the metals not directly participating in the cell reaction (Pt) have disappeared from the final Eq. (3.1.49). This result is of general significance, i.e. the EMFs of cell reactions involving oxidation-reduction processes do not depend on the nature of the metals where those reactions take place. The situation is, of course, different in the case of a metal directly participating in the cell reaction (for example, silver in the above case). 

Coumarin (7.88) is a well-known 6-lactone (six-membered ring) of natural origin found in various preparations such as some tobaccos, alcoholic beverages, and cosmetics. Besides reactions of oxidation, reduction, and conjugation, coumarin is also subject to lactone hydration in vivo and in the presence of microsomes [170-174], The resulting metabolites include ortho-coumaric acid (7.89) formed directly from coumarin, 3-(2-hydroxyphenyl)-propionic acid (7.91) formed following reduction of coumarin to dihydrocou-... 

Calcinm glectrowinning in piutniiium production. A potential application of inorganic membranes in radioactive waste treatment is in the industrially practiced direct oxide reduction process. In this process plutonium oxide is calciothermit y reduced to plutonium in the presence of calcium chloride according to the following reaction ... 

The effluent salt is the radioactively contaminated calcium chloride saturated with calcium oxide which can not be discarded as-is. Thus it is desirable to cathodically reduce calcium oxide to calcium which can then be recycled back to the direct oxide reduction process. The primary difficulty in obtaining a cathodic calcium deposit is due to the evolution of carbonaceous anodic gases which encourage various reverse reactions in the cell leading to loss of deposited calcium. 

Complexation/decomplexation of metal ions or of neutral organic molecules, protonation/deprotonation reactions, and oxidation/reduction processes can all be exploited to alter reversibly the stereoelectronic properties of one of the two recognition sites, thus affecting its ability to sustain noncovalent bonds [30-34, 41]. These kinds of switchable [2 catenanes can be prepared following the template-directed synthetic strategy illustrated in Figure 5, wherein one of the two macrocyclic components is preformed and then the other one is clipped around it with the help of noncovalent bonding interactions. 

Cigarette smoke composition is dependent on two major processes occurring during the smoking of tobacco the direct transfer by vaporization of volatile tobacco components directly to the smoke and the pyrogenesis of smoke components from tobacco components. The pyrogenesis involves a variety of reactions, including oxidation, reduction, aroma-tization, hydration, dehydration, condensation, cyclization, polymerization, depolymerization, etc. 

Recent studies with copper phenanthroline complexes expand on the possibilities for site-directed oxidation-reduction chemistry of copper complexes. Cu(ii)(l,10-phenanthroline)2, alone or tethered to various DNA-binding domains, causes DNA strand scission in vitro in the presence of reductants, which involves the formation of the hydroxyl radical or its equivalent." - Upon reaction of Cu(ii)(Phen)2 with tumor cells, it is likely that the complex binds directly to DNA, acting as a site-directed catalyst for the generation of oxyradi-cals. ... 

Cr(rV) is a very unstable intermediate. According to Beattie and Haight Its reactions, including oxidation, reduction and disproportionation, are too fast to admit to its direct detection". However, KaCrF has been prepared and was shown to be iso-morphous with KaMnF Salts of tetrahedral CrOj" are also known ... 

According to the authors, the terms haif-reaction or oxidation-reduction reaction can be used for this eiectron exchange reaction. The term haif-reaction, which is often used in this document, stresses the fact that if a redox coupie reacts, e.g., in the direction of oxidation, at least one other couple must react in the direction of reduction. This term is derived from redox-chemistry in solution-based reactions, however it is still of educational interest for electrochemists given that at least two half-reactions are always occurring simultaneously, one at the anode and the other at the cathode. 

The ready reversibility of this reaction is essential to the role that qumones play in cellular respiration the process by which an organism uses molecular oxygen to convert Its food to carbon dioxide water and energy Electrons are not transferred directly from the substrate molecule to oxygen but instead are transferred by way of an electron trans port chain involving a succession of oxidation-reduction reactions A key component of this electron transport chain is the substance known as ubiquinone or coenzyme Q... 

Direct reaction of oxygen with most organic materials to produce radicals (eq. 13) is very slow at moderate temperatures. Hydrogen-donating antioxidants (AH), particularly those with low oxidation—reduction potentials, can react with oxygen (eq. 14), especially at elevated temperatures (6). 

Several species of bacteria under suitable conditions cause / -butyraldehyde to undergo the Canni22aro reaction (simultaneous oxidation and reduction to butyric acid and butanol, respectively) this reaction can also be cataly2ed by Raney nickel (7). The direct formation of butyl butyrate [109-21 -7] or isobutyl isobutyrate [97-85-8](Vish.ch.erik.o reaction) from the corresponding aldehyde takes place rapidly with aluminum ethylate or aluminum butyrate as catalyst (8). An essentially quantitative yield of butyl butyrate, CgH2 02, from butyraldehyde has been reported usiag a mthenium catalyst, RuH,[P(C,H,)3], (9). 

Hydroxylamine sulfate is produced by direct hydrogen reduction of nitric oxide over platinum catalyst in the presence of sulfuric acid. Only 0.9 kg ammonium sulfate is produced per kilogram of caprolactam, but at the expense of hydrogen consumption (11). A concentrated nitric oxide stream is obtained by catalytic oxidation of ammonia with oxygen. Steam is used as a diluent in order to avoid operating within the explosive limits for the system. The oxidation is followed by condensation of the steam. The net reaction is... 

Oxidation—Reduction. Redox or oxidation—reduction reactions are often governed by the hard—soft base rule. For example, a metal in a low oxidation state (relatively soft) can be oxidized more easily if surrounded by hard ligands or a hard solvent. Metals tend toward hard-acid behavior on oxidation. Redox rates are often limited by substitution rates of the reactant so that direct electron transfer can occur (16). If substitution is very slow, an outer sphere or tunneling reaction may occur. One-electron transfers are normally favored over multielectron processes, especially when three or more species must aggregate prior to reaction. However, oxidative addition... 

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