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Home Heat Accumulators Novel-ester-modified-poly-alkylene-carbonate-polyahls

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 Novel ester-modified poly(alkylene carbonate) polyahls

Details
Inventors: Harris, Robert F.;
Assignee: The Dow Chemical Company (Midland, MI)
Primary Examiner: McCamish; Marion C.
Assistant Examiner: Sridharan; Anang
Attorney, Agent or Firm:

Ester-modified poly(alkylene carbonate) polyahls comprising the residues of at least one polyahl, polyalkyleneoxy moieties, poly(alkylene carbonate) moieties, the residues of at least one ester of a carboxylic acid, and a plurality of active hydrogen end group are disclosed. The ester-modified poly(alkylene carbonate) polyahl has a number average molecular weight higher than the number average molecular weight of any known poly(alkylene carbonate) polyahl comprising the same monomeric components. Also disclosed are isocyanate-functional prepolymers of these ester-modified poly(alkylene carbonate) polyahls formed by reactions of the ester-modified poly(alkylene carbonate) polyahls of this invention with excess organic polyisocyanates. Urethane/urea polymers formed by the reactions of the isocyanate-functional prepolymers with polyahls are also disclosed. Also disclosed are urethane/urea polymers comprising the residue of at least one ester-modified poly(alkylene carbonate) polyahl of this invention, the residue of a polyisocyanate and the residue of at least one other polyahl selected from the group consisting of polyamines, polymercaptans and polyfunctional hydroxyl compounds. The novel compositions of this invention are useful in urethane/urea polymer applications such as foams, elastomers, plastics, adhesives, coatings and the like.

DETAILED DESCRIPTION OF THE INVENTION The ester-modified poly(alkylene carbonate) polyahl compositions of this invention can be prepared by the reactions of poly(alkylene carbonate) polyahls with one or more modifiers.
During these reactions the modifier is chemically combined to the poly(alkylene carbonate) polyahl.
Poly(alkylene carbonate) polyahls are randomized polymers having a plurality of carbonate moieties and a plurality of active hydrogen moieties and optionally other moieties such as di- and higher polyalkyleneoxy, units.
An alkylene carbonate moiety is a repeating unit which has an alkylene group bound to a carbonate moiety.
An active hydrogen moiety is a moiety containing a hydrogen atom which because of its position in the moiety displays significant activity according to the Zerewitnoff test described by Kohler et al.
in the Journal of American Chemical Society, 49, 3181 (1927).
Illustrative of such active hydrogen moieties are --COOH, --OH, --NH.
sub.
2, --NH--, --CONH.
sub.
2, --SH and --CONH--.
Alkyleneoxy moiety refers herein to a repeating unit which has an alkylene group bound to oxygen.
Alkylene carbonate and alkyleneoxy moieties are respectively represented by the following formulae: ##STR1## wherein R.
sup.
2 is as hereinafter defined.
Preferred poly(alkylene carbonate) polyahls are random polymers which correspond to the formula ##STR2## wherein R.
sup.
1 is separately in each occurrence an n-valent hydrocarbon radical or hydrocarbon radical which can contain one or more heteroatoms of O, N or S; R.
sup.
2 is separately in each occurrence hydrogen, halogen, a nitro group, a cyano group, a C.
sub.
1-20 hydrocarbyl group or a C.
sub.
1-20 hydrocarbyl group substituted with one or more halo, cyano, nitro, thioalkyl, tert-amino, alkoxy, aryloxy, aralkoxy, carbonyldioxyalkyl, carbonyldioxyaryl, carbonyldioxyaralkyl, dioxyaralkyl, alkoxycarbonyl, aryloxycarbonyl, aralkoxycarbonyl, alkylcarbonyl, arylcarbonyl, aralkylcarbonyl, alkylsulfinyl, arylsulfinyl, aralkylsulfinyl, alkylsulfonyl, arylsulfonyl, or aralkylsulfonyl group; X is separately in each occurrence S, O, NH, ##STR3## A is separately in each occurrence ##STR4## combinations thereof or a covalent bond; Q is separately in each occurrence O, S or NH provided that all carbonate moieties are internal because terminal carbonate moieties are unstable and form OH moieties by the elimination of CO



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