M. Ionescu et al., POLYETHER TRIOLS, TETRAHYDROFURAN-ALKYLENEOXIDES COPOLYMERS FOR FLEXIBLE POLYURETHANE FOAMS, Cellular polymers, 14(3), 1995, pp. 203-229
The study presents a new process for the synthesis of polyether triols
, tetrahydrofuran (THF)-alkyleneoxides copolymers for flexible polyure
thane foams, by the cationic ring opening copolymerization of THF and
propyleneoxide (PO) and/or ethyleneoxide (EO), initiated by glycerol o
r trimethylolpropane as starters. By using the principles of ''activat
ed monomer mechanism'', (a new achievement in the cationic polymerizat
ion of alkyleneoxides), in the adopted reaction conditions, the equili
brium polymerization of THF and the formation of undesired cyclic olig
omers (from alkyleneoxides) are suppressed. Thus, a great variety of c
opolyether triols having molecular weight 3000-6000 were synthesized (
THF-PO, THF-EO, THF-EO-PO, THF-PO-EO etc.). The excellent properties o
f the flexible polyurethane foams based on these new telechelic interm
ediates, as compared with classical polyether triols based exclusively
on PO and EO, were investigated.