Hydrogen peroxide, 30% concentration compounds

Because of the ease of oxidation of protactinium(IV) and uranium(IV), peroxides and peroxo complexes are limited to their higher oxidation states. The compounds M04"JcH20 precipitated from dilute acid solutions of neptunium(IV) and plutonium(IV) by hydrogen peroxide appear to be actinide(IV) compounds. Soluble intermediates of the type [Pu( U-02)2Pu]4+ are formed at low hydrogen peroxide concentrations. 

Figure 6 shows the variation of peroxide concentration in methyl ethyl ketone slow combustion, and similar results, but with no peracid formed, have been found for acetone and diethyl ketone. The concentrations of the organic peroxy compounds run parallel to the rate of reaction, but the hydrogen peroxide concentration increases to a steady value. There thus seems little doubt that the degenerate branching intermediates at low temperatures are the alkyl hydroperoxides, and with methyl ethyl ketone, peracetic acid also. The tvfo types of cool flames given by methyl ethyl ketone may arise from the twin branching intermediates (1) observed in its combustion. 

Permanent hair colors can be achieved with tint shampoos. The shampoo base is adjusted to an alkaline pH and contains oxidation dye intermediates. Before application, it is mixed with hydrogen peroxide or a hydrogen peroxide addition compound. In comparison with oxidation hair dyes, tint shampoos employ lower concentrations of base and oxidant. This suppresses the simultaneous bleaching process that occurs during dyeing (see Section 5.4.2). As a result, damage to the keratin in hair is diminished, but the uniform coloring action is lost. 

The reaction of piperidine conjugated dehydrogenation with hydrogen peroxide [99] opens the way to dehydrogenation of natural compounds, which include piperidine fragments. As shown by experimental data, pyridine yield increases from 45% to 65.2% with hydrogen peroxide concentration from 20% to 25%, respectively, with reaction selectivity above 98%. A further increase of H202 concentration reduces pyridine yield to 59%. It follows from these... 

Miyake, C., and Asada, K., 1996, Inactivation mechanism of ascorbate peroxidase at low concentrations of ascorbate hydrogen peroxide decomposes Compound 1 of ascorbate peroxidase. Plant Cell Physiol. 37 423n430. 

The reaction velocity of this compound is probably comparatively slow, since Sumner and Gjessing (66) found, for horse-radish peroxidase, that increasing the hydrogen peroxide concentration above an optimal concentration gave a successive decrease in the amoimt of purpurogallin formed. However, it was not established whether the decrease was due to the formation of compound III or to destruction of the enzyme. 

For this reaction, charcoal is a catalyst if this is omitted and hydrogen peroxide is used as the oxidant, a red aquopentammino-cobalt(lll) chloride, [Co(NH3)jH20]Cl3, is formed and treatment of this with concentrated hydrochloric acid gives the red chloro-p0itatnmino-coba. t(lll) chloride, [Co(NH3)5Cl]Cl2. In these latter two compounds, one ammonia ligand is replaced by one water molecule or one chloride ion it is a peculiarity of cobalt that these replacements are so easy and the pure products so readily isolated. In the examples quoted, the complex cobalt(III) state is easily obtained by oxidation of cobalt(II) in presence of ammonia, since... 

The study of the chemical behavior of concentrated preparations of short-Hved isotopes is compHcated by the rapid production of hydrogen peroxide ia aqueous solutions and the destmction of crystal lattices ia soHd compounds. These effects are brought about by heavy recoils of high energy alpha particles released ia the decay process. 

Toxic or malodorous pollutants can be removed from industrial gas streams by reaction with hydrogen peroxide (174,175). Many Hquid-phase methods have been patented for the removal of NO gases (138,142,174,176—178), sulfur dioxide, reduced sulfur compounds, amines (154,171,172), and phenols (169). Other effluent treatments include the reduction of biological oxygen demand (BOD) and COD, color, odor (142,179,180), and chlorine concentration. 

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