In the presence of furnace black (HAF) treated with agents such as benzoyl peroxide (Bz
2O
2), 2, 2-diphenyl-l-picrylhydrazyl, nitrous oxide, diazomethane, hydrogen peroxide and nitric acid, the products obtained by the reaction of ethylene glycol with Bz
2O
2 at 45°C have been examined and compared with those of the untreated HAF. The saponification of Bz
2O
2- treated HAF to convert benzoate group into surface phenolic hydroxyl has also been carried out to examine the extent of the ability to cause the C-C bond cleavage of the glycol using the resulting carbon black.
In many cases it is found that the treated carbon blacks show decrease in the ability to cause the C-C cleavage in compared with that of the untreated HAF. For example, in the presence of treated samples with Bz
2O
2, nitrous oxide and nitric acid, the oxidation of the glycol with Bz
2O
2 gives mainly acetaldehyde. However, in the presence of the hydrolyzed sample, the recovery of a greater part of ability to convert the glycol into formaldehyde is observed.
The results indicate that the benzonoidal rings and a part of phenolic hydroxyl groups present at the edge of micrographitic platelets on carbon black surface may be responsible for the C-C bond cleavage reaction.
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