The effect of various carbon blacks on the thermal polymerization of styrene and other monomers was studied.
Styrene could be graft-polymerized onto oil furnace blacks in the absence of initiators, but channel type blacks were less effective to form graft-polymer.
In addition, use of furnace blacks which were oxidized with hot nitric acid, treated with benzoyl peroxide or heated at 1, 500°C under nitrogen atmosphere was not desirable; it caused marked reduction in grafting ability. In particular, a significant drop in conversion rate of styrene in the presence of the carbon black treated with hot nitric acid was observed.
Furthermore, graft polymerization of styrene was retarded by using benzoyl peroxide as an initiator. This fact suggested that free radicals generated by the decomposition of the peroxide prefer to react and combine exclusively with the surface of carbon black. On the basis of these phenomena and the free-radical character of the surface of carbon blacks, a probable mechanism for the graft-polymerization of styrene was presented.
On the other hand, by using α, α'-azobisisobutyronitrile the monomers such as acrylonitrile, vinyl acetate and methacrylates could be easily graft-polymerized onto the surface of furnace blacks in adequate solvent.
Carbon-styrene graft polymer based on furnace black had good dispersion in benzene, toluene or trichloroethylene. However, it had some faults similar to those of styrene polymer. In order to improve these properties, graft polymerizations of styrene with other monomers were also studied.
View full abstract