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Oxidation continued

Thus ethylene is oxidized continuously through a series of oxidation—reduction reactions (87,88). The overall reaction is... [Pg.51]

The formation of pores appears to start along the sub-grain boundaries of the metal, followed by the development of additional pores within the subgrains. Growth of oxide continues on a series of hemispherical fronts centred on the pore bases, provided that the effective barrier-layer thickness between the metal surface and the electrolyte within the pores, represented by the hemisphere radius, is less than 1-4 nm/V. As anodic oxidation proceeds at... [Pg.691]

B. Electrophilic Reactions of the P=0 and P=S Groups. Hydrolysis studies with phosphine oxides continue to reveal problems associated with the role of pseudorotational processes in determining mechanism. The failure of benzyldiphenylphosphine oxide (36) to exchange when hydrolysed in under bimolecular conditions has been reported. ... [Pg.62]

The Ce(III) thus obtained will next be oxidized at its decomposition potential (nearly 1.4 V) this overall process of direct and indirect oxidation continues until Fe(II) has been completely converted into Fe(III) at this stage no Ce(III) remains, but only the amount of Ce(IV) previously added in order to stop the anodic oxidation in time the potential of the Pt-WE (vs. SCE-RE) should automatically interrupt the electrolysis beyond say 1.5 V, i.e., well below the decomposition potential of H20. [Pg.236]

The anodic oxidation of sheet aluminum has been used for a long time to protect aluminum against corrosion by a well-adhering oxide layer. Porous oxide layers are formed if acid electrolytes are used that can redissolve the aluminum oxide (mostly sulfuric or phosphoric acid). A compact oxide layer is formed at the beginning of the electrolysis (Fig. 20.3). Simultaneously, the current decreases, due to the electric resistance of the oxide. Subsequently follows a process in which the oxide is redissolved by the acid, and the current increases until it reaches a steady state. The electrochemical oxidation continues to take place with formation of pores. At the end of a pore, where it has the largest curvature, the electric field has its largest gradient and the process of redisolution is fastest. [Pg.242]

Chronological Table of the Main Concepts and Experimental Findings of Chain Theory of Hydrocarbon Oxidation—continued... [Pg.39]

The photochemical after-effect, considering that after light is switched off, the light oxidation continues for some time (time of chain growth), also indicates the chain nature of the process. This after-effect was observed in the photochemical oxidation of... [Pg.57]

The acyl radicals formed in ketone photolysis are excited and, therefore, rapidly splits into CO and alkyl radical (in the gas phase). Since aldehydes and ketones are products of oxidation, continuous hydrocarbon photooxidation is an autoaccelerated process. [Pg.156]

Synthetic studies of various cyclic phosphine oxides continue to be published. Thus a methanolic work-up leads to an 88% yield of 1-methylphospholen 1-oxides (6) from dichloro(methyl)phosphine, and detailed S1P n.m.r. and mass spectra have been described.10 The oxides (7) and (8) have been prepared11 as shown. Structural... [Pg.72]

Figure 3.38. Experimental densities of titanium oxides (continuous lines). The upper dotted line gives the values computed for a 100% occupancy of the cation sites in the NaCl structure type (from Hyde and Andersson 1989). Figure 3.38. Experimental densities of titanium oxides (continuous lines). The upper dotted line gives the values computed for a 100% occupancy of the cation sites in the NaCl structure type (from Hyde and Andersson 1989).
P-oxidation continues only as far as a medium-chain CoA derivative, which is transported out of the peroxisome as its carnitine ester. It then enters the mitochondria where P-oxidation continues to produce acetyl-CoA. The acetyl-CoA, which is produced in the peroxisome, is also transported out for oxidation in the mitochondria (Appendix 7.4). [Pg.138]

For oxidation of iron to occur at high temperatures, the oxygen partial pressure must be above that of the dissociation pressure of the appropriate corrosion products. For example, at ca. 700 °C, an oxygen partial pressure of greater than 10 Pa is required for wiistite to form. In air, of course, this condition is readily satisfied, at least initially. As oxidation continues and the film thickens and becomes coherent, an oxygen gradient across the film is established and the composition of the corrosion layer changes. [Pg.495]

Active crystal face of vanadyl pyrophosphate for selective n-butane oxidation—Continued selectivity, 162,164r selectivity vs. face, 165,166/... [Pg.449]

Autoxidation of Chloroprene. The oxidation was autocatalytic and up to about 5 mole % oxidation—i.e., 5 moles of oxygen absorbed per 100 moles of chloroprene initially present—the quantity (mole % oxidation)172 was a linear function of time, as observed by Kern (10). Beyond this extent the oxidation continued at a rather greater rate than given by this relation and was still accelerating at 25 mole % oxidation. Values of K in the expression... [Pg.151]


See other pages where Oxidation continued is mentioned: [Pg.112]    [Pg.525]    [Pg.160]    [Pg.469]    [Pg.439]    [Pg.571]    [Pg.292]    [Pg.218]    [Pg.219]    [Pg.220]    [Pg.222]    [Pg.218]    [Pg.499]    [Pg.85]    [Pg.75]    [Pg.95]    [Pg.124]    [Pg.34]    [Pg.90]    [Pg.1478]    [Pg.105]    [Pg.11]   


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Acetylene oxidation—continued

Acid continued) conjugated oxidation

Acid continued) oxidation rate

Acid continued) oxidative degradation

Addition reactions (continued oxidative

Alcohols continuous-flow aerobic oxidation

Alkenes continued) oxidation

Aluminium alloys continued oxide film

Aluminium continued oxide film

Aluminium continued oxides

Azines—continued N-oxidation, effect on reactivity

Bromine (continued oxidations states

Carbon continued oxidation

Cast iron continued oxidation

Catalyst [continued) oxide

Catalyst [continued) titanium oxide

Catalyst [continued) zirconium oxide

Chemicals continued propylene oxide

Continuous fiber reinforced glass composites with oxide fibers

Continuous fine oxide fibers

Continuous metal-free aerobic oxidations

Continuous oxidation

Continuous oxidation

Continuous-flow microreactors oxidations

Covalent hydration—continued of quinazoline 3-oxides

Electrodes continued oxide

Enzymes continued oxidizing

Ethanol—continued oxidation

Hydrogen separation continued) oxidation

Hydrogen separation continued) with oxidative

Infrared (continued oxidized

Iron continued oxidation

Iron oxide process continuous

Lactate, continued oxidation

Lysine (continued oxidation

Metal complexes—continued oxidation

Metal complexes—continued oxidation-reduction potentials

Metal complexes—continued oxidation-reduction reactions

Methane continued) oxidation

Methane continued) oxide

Methanol—continued oxidation

Nickel continued oxides

Nitric oxide, continued

Nitric oxide, continued signaling

Nitropyridines—continued 1-oxides

Nucleophilic substitution—continued N-oxidation, effect

Nucleophilic substitution—continued of pyridine N-oxides, kinetics for

Nucleophilic substitution—continued of quinoline N-oxides

Octanes—continued oxidation

Oxidation continued reactions

Oxidation continued sulphur

Oxidation continued tantalum

Oxidation continued uranium

Oxidation continued volume change

Oxidation continued zirconium

Oxidation continued) selenium

Oxidation continuous selective

Oxidation—continued peroxide

Oxidation—continued with hydrogen peroxide

Oxidation—continued with lead tetraacetate

Oxidation—continued with mercuric acetate

Oxidation—continued with oxygen

Oxidation—continued with ozone

Oxidation—continued with potassium ferricyanide

Oxidation—continued with selenium dioxide

Oxidation—continued with sodium dichromate

Oxidation—continued with sodium persulfate

Oxide films continued

Oxide films continued cation vacancies

Oxide films continued experimental techniques

Oxide films continued formation

Oxide films continued linear rate

Oxide films continued passive

Oxide films continued porous

Oxide films continued protective

Oxide films continued voids

Oxide films continuous

Photosensitized Singlet Oxygen Oxidations in Continuous Flow

Processes continuous aldehyde oxidation

Proteins - continued oxidation

Pyridine 1 -oxide—continued reactions

Pyridine 1 -oxide—continued reactions with

Pyridine 1 -oxide—continued substitution reactions

Pyridine 1-oxides—continued

Pyridine 1-oxides—continued reactivity

Pyridine 1-oxides—continued reduction

Pyridines, 1-oxides—continued sodium

Pyrolysis continued) partial oxidation

Steam continued oxidation effects

Steels continued oxidation

Steels continued oxidation resistance

Sulfur continued oxidation catalyst

Tannins (continued oxidation

Thallium (continued oxidation

Transition Metal-Catalyzed Aerobic Oxidations in Continuous Flow

Tryptophan—continued oxidation

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