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RESEARCH PRODUCT

Solid-state polymerization of oxetanes. II. Investigation of the growth of the polymer phase as related to the mechanism of polymerization

G. WegnerB. Keggenhoff

subject

Kinetic chain lengthEnd-groupChain-growth polymerizationMaterials sciencePolymerizationPolymer chemistryRadical polymerizationtechnology industry and agriculturePrecipitation polymerizationChain transfermacromolecular substancesIonic polymerization

description

The radiation-induced solid-state polymerization of 3,3-bischloromethyloxetane (BCMO) was investigated by direct observation of the development of the morphology of the growing polymer phase in single crystals of the monomer. Electron microscopy shows that the polymerization gives rise to amorphous polymer in the first step. The polymer forms irregular platelets which aggregate into larger units without reflecting the crystalline order of the monomer. Subsequent to polymerization, the amorphous polymer crystallizes to the β-modification of poly-BCMO. If the partially polymerized crystals are extracted by solvents of the monomer, crystallization of the polymer is enhanced, and morphological artifacts arise which were previously mistaken for the true morphology of the “as polymerized” polymer. The copolymerization behavior of solid solutions of 3-ethyl-3-chloromethyloxetane (ECMO) and BCMO does not differ from the liquid bulk copolymerization with respect to copolymer composition, which is different from the composition of the monomer mixture. It is concluded that the polymer chains grow in noncrystalline zones as in a polymerization in the liquid state by which amorphous polymer is formed. No lattice control was observable in this solid-state polymerization.

https://doi.org/10.1002/pol.1973.180110410