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Studies on the formation of novel copolyesters containing naphthalene and aralkyloxy structures
Author(s) -
Sun Y.M.,
Wang C.S.
Publication year - 1995
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.1995.070580712
Subject(s) - copolyester , condensation polymer , differential scanning calorimetry , polymer chemistry , materials science , glass transition , aryl , nucleophilic substitution , naphthalene , catalysis , chemistry , alkyl , organic chemistry , polyester , polymer , composite material , physics , thermodynamics
Copolyesters containing naphthalene structure were synthesized from bis(hydroxyethyl)naphthalate (BHEN) and various aralkyloxy diols. The starting bis(4‐(2‐hydroxyethoxy)aryl) compounds were derived from a nucleophilic substitution of various bisphenols with ethylene carbonate in the presence of potassium iodide (KI). Copolyesters having intrinsic viscosities of 0.50 to 0.60 dL/g were obtained by melt polycondensation in the presence of metallic catalysts. The effects of reaction temperature and time on the formation of copolyesters were investigated in order to obtain an optimum condition for copolyester manufacturing. The optimal reaction temperature and time were found to be 290 to 310°C and 90 to 120 min, respectively. Most of these copolyesters have better solubilities than polyethylene naphthalate (PEN) in aprotic solvents such as N ‐methyl‐2‐pyrrolidone or m ‐cresol. The thermal properties of the copolyesters were investigated by differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA). Glass transition temperatures of these copolyesters were in the range of 90 to 141°C, and 10% weight loss values in nitrogen were all above 460°C. © 1995 John Wiley & Sons, Inc.