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 in | Journal of polymer research Vol. 22; no. 3; p. 1 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Dordrecht
Springer Nature B.V
01.03.2015
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Online Access | Get full text |
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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. |
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ISSN: | 1022-9760 1572-8935 |
DOI: | 10.1007/s10965-015-0655-0 |