AbstractCarbochain and heterochain polyamides are highly reactive compounds and may be quite easily converted to various polymer analogs, including compounds with graft side chains. We have studied the relations in the polyoxyethylation of heterochain and carbochain polyamides of various structure under different conditions. Under heterogeneous conditions the reaction takes place not only at the surface, but in the entire body of the film or fiber, although not to the same degree. On heterogeneous polyoxyethylation of heterochain polyamides graft polymers were obtained with up to 55% content of polyethylene oxide, with varying polyethylene oxide chain lengths and with different degrees of substitution of the groups. The formation of polyoxyethylated polyamides with high polyethylene oxide contents is facilitated by the use of a large excess of ethylene oxide and a lower degree of orientation of the films and fibers. In the polyoxyethylation of heterochain polyamides, as a result of crosslinking insoluble products may form which are greatly swelled in the various solvents. The branching and crosslinking of the macromolecules has been found to result from the reaction of the terminal carboxyl groups of the polyamides and the hydroxyl groups of the polyethylene oxide graft. On polyoxyethylation of polyamides not containing terminal carboxyl groups non‐cross‐linked, soluble, graft polymers are formed. In the heterogeneous polyoxyethylation of Polyacrylamide films, graft polymers with up to 65% polyethylene oxide content were obtained. In this case the reaction is also accompanied by the formation of crosslinks. In the reaction process one or both of the hydrogens of an amide group may be replaced by polyethylene oxide chains.
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