Aliphatic-aromatic poly(ester-carbonate)s obtained from simple carbonate esters, [alpha],[omega]-aliphatic diols and dimethyl terephthalate

Two reaction pathways for synthesis of high molar mass (M^sub w^ above 50 000 g/mol) aliphatic-aromatic poly(ester-carbonate)s were elaborated. Simple organic carbonates such as dimethyl carbonate or propylene carbonate were used as carbonate linkage sources and dimethyl terephthalate as the precurs...

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Published inJournal of polymer research Vol. 22; no. 3; p. 1
Main Authors Mazurek, M, Bruliski, T, Tomczyk, K, Parzuchowski, P, Florjaczyk, Z, Plichta, A, Rokicki, G
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Nature B.V 01.03.2015
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Summary:Two reaction pathways for synthesis of high molar mass (M^sub w^ above 50 000 g/mol) aliphatic-aromatic poly(ester-carbonate)s were elaborated. Simple organic carbonates such as dimethyl carbonate or propylene carbonate were used as carbonate linkage sources and dimethyl terephthalate as the precursor of ester linkages. 1,4-Butanediol, 1,5-pentanediol, 1,6-hexanediol and 1,10-decanediol were used as diol monomers. To adjust the carbonate units content in the copolymer, solid alkylene bis(methylcarbonate) was used as a semiproduct instead of volatile dimethyl carbonate. In case of usage propylene carbonate as a starting material the process can be carried out in one pot without the need for isolation of the semiproduct. The obtained copolymers based on 1,4-butanediol, containing ca. 50 mol.% of carbonate units exhibited better mechanical strength (37 MPa) than commercially available aliphatic-aromatic copolyester Ecoflex^sup ^ keeping the thermal properties at the same level.
ISSN:1022-9760
1572-8935
DOI:10.1007/s10965-015-0655-0