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Cobalt peroxide

Burdo and Seitz reported in 1975 the mechanism of the formation of a cobalt peroxide complex as the important intermediate leading to luminescence in the cobalt catalysis of the luminol CL reaction [116]. Delumyea and Hartkopf reported metal catalysis of the luminol reaction in chromatographic solvent systems in 1976 [117], while Yurow and Sass [118] reported on the structure-CL correlation for various organic compounds in the luminol-peroxide reaction. [Pg.22]

Howell, O.R. (1923) The catalytic decomposition of sodium hypochlorite by cobalt peroxide. Proceedings of the Royal Society, 104A, 134. [Pg.345]

In a recent mechanistic study it was shown that ferf-butyl hydroperoxide acts most likely as a precursor for the formation of a cobalt peroxide intermediate (entry 3)... [Pg.284]

Cobalt Dioxide, Cobalt Peroxide, Co02, is obtained in the hydrated condition as a greenish black precipitate by treating aqueous solutions of cobaltous salts with iodine and sodium hydroxide.12 It is also obtained by acting on a cobaltous salt with a hypochlorite.13 It decomposes at 100° C., and when washed undergoes partial reduction. [Pg.50]

SYNS C.I. 77323 COBALTIC OXIDE COBALT OXIDE (8CI,9CI) COBALT(3+) OXIDE COBALT PEROXIDE COBALT SESQIOXIDE COBALT SESQUIOXIDE COBALT TRIOXIDE DICOBALT OXIDE DICOBALT TRIOXIDE... [Pg.380]

More common oxidation reagents are oxygen in the presence of cobalt peroxide [1136], manganese dioxide [Si3], barium manganate [S53], silver permanganate [897], and nickel peroxide [936] (equation 495). [Pg.234]

More intensive dehydrogenation of primary amines having two hydrogen atoms on the adjacent carbons leads to nitriles. Such dehydrogenations are accomplished by argentic oxide cobalt peroxide [1136], nickel peroxide [936], lead tetraacetate [443, 444], sodium hypochlorite [692], potassium ferricyanide [924], and potassium ruthenate [196] (equation 513). [Pg.241]

Cobalt peroxide 42S0 C02O3 Cobaltlc oxide cobalt sesquloxide. [Pg.7]

C.l. 77323 Cobalt black Cobalt oxide Cobalt oxide (C02O3) Cobalt peroxide Cobalt sesqioxide Cobalt sesquioxide Cobalt trioxide Cobalt(3+) oxide Cobalt(lll) oxide Cobaitic oxide Dicobalt oxide Dicobalt trioxide EINECS 215-156-7. A pigment used in coloring enamels and glazing pottery. Black solid insoluble In H2O. soluble in H2SO4. Atomergic Chemetals Cerac Noah Chem. [Pg.154]

The effect of ionic environment on the rate of diffusion controlled e"aq reactions is revealed when one compares the experimental rate constants with the calculated values. In Table I the highly charged bis-pentacyano cobaltic peroxide (I) is much more reactive than expected for a pentavalent anion (1.11). It has been claimed (19) that polyvalent anions exhibit a lower effective charge in their kinetic behavior than expected from their structural formulae. We have checked the salt effect on the reaction of I + e m and compared it with the NOjf e m reaction. The results presented in Table IV and Figure 1 show that nitrate ions possess a normal salt effect, a result previously obtained by competition kinetics (15, 17). On the other hand, the salt effect of the I + e"aq reaction shows that this bis-pentacyano cobaltic peroxide ion has an... [Pg.87]

The choice of initiator will depend on the fabrication requirements. For low-temperature curing, cobalt-peroxide combinations often are used. The benzoyl peroxide-tertiary amine system is used at low temperatures when oxygen inhibition is a problem. Higher-temperature processes generally rely on the uncatalyzed thermal initiation of initiators such as cumene hydroperoxide or dilauryl peroxide. [Pg.656]


See other pages where Cobalt peroxide is mentioned: [Pg.16]    [Pg.300]    [Pg.1591]    [Pg.313]    [Pg.7]    [Pg.7]    [Pg.16]    [Pg.358]    [Pg.870]    [Pg.61]    [Pg.187]    [Pg.359]    [Pg.620]    [Pg.68]   


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