Polymerization of Ethylene Terephthalate Cyclic Oligomers with Antimony Trioxide
Author(s) -
Ji Ho Youk,
R. P. Kambour,
William J. MacKnight
Publication year - 2000
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/ma991838d
Subject(s) - antimony trioxide , polymerization , ethylene glycol , antimony , dichloromethane , materials science , ethylene , nuclear chemistry , bismuth , thermal decomposition , polymer chemistry , chemistry , catalysis , polymer , organic chemistry , solvent , composite material , fire retardant , metallurgy
Conditions for polymerizing ethylene terephthalate cyclic oligomers (ETCs) with the catalyst antimony trioxide were investigated with the ultimate goal in mind of using ETCs to produce high-performance poly(ethylene terephthalate) (PET) composites. The ETCs used were prepared both by a direct synthesis method and by cyclodepolymerization (CDP) in dilute solution. ETCs prepared exhibited a distribution of oligomeric species displaying a broad melting range, the uppermost end of which lies at 290 °C. In the case of ETCs prepared by CDP, purified ETCs (p-ETCs) were prepared by eliminating remaining impurities including linear oligomers and cyclic oligomers containing the diethylene glycol (DEG) unit using dichloromethane and tetrahydrofuran. A homogeneous mixture of ETCs prepared by the direct synthesis method or p-ETCs with antimony trioxide was successfully polymerized to high molecular weight (MW) PET (Mn ≥ 25 000) at 293 °C within 15 min. The lower the contents of remaining impurities, the higher the MW ...
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom