TY - JOUR
T1 - A novel high-temperature naphthyl-based phthalonitrile polymer
T2 - Synthesis and properties
AU - Zhao, Fenghua
AU - Liu, Ruojin
AU - Kang, Chao
AU - Yu, Xiaoyan
AU - Naito, Kimiyoshi
AU - Qu, Xiongwei
AU - Zhang, Qingxin
PY - 2014
Y1 - 2014
N2 - A novel naphthyl-based phthalonitrile monomer, 1,6-bis(3,4-dicyanophenoxy) naphthalene (1,6-BDCN), was prepared, and the phthalonitrile resin was cured with 4,4′-diaminodiphenyl ether (ODA) via two steps, namely, preparation of prepolymer and postcuring prepolymer at elevated temperatures. The 1,6-BDCN polymer might form triazine and phthalocyanine rings as demonstrated by FTIR spectra. The prepolymer shows fine solubility in organic solvents. The 1,6-BDCN polymer exhibits excellent structural integrity and superior thermal stability as indicated by thermogravimetric analysis (TGA). Dynamic mechanical analysis (DMA) revealed that the phthalonitrile resin has a high storage modulus and glass transition temperature (Tg). The water uptake is about 3% by weight after submersion in boiling water for 50 hours. The influence of curing processes on thermal stability and flame retardancy was also explored.
AB - A novel naphthyl-based phthalonitrile monomer, 1,6-bis(3,4-dicyanophenoxy) naphthalene (1,6-BDCN), was prepared, and the phthalonitrile resin was cured with 4,4′-diaminodiphenyl ether (ODA) via two steps, namely, preparation of prepolymer and postcuring prepolymer at elevated temperatures. The 1,6-BDCN polymer might form triazine and phthalocyanine rings as demonstrated by FTIR spectra. The prepolymer shows fine solubility in organic solvents. The 1,6-BDCN polymer exhibits excellent structural integrity and superior thermal stability as indicated by thermogravimetric analysis (TGA). Dynamic mechanical analysis (DMA) revealed that the phthalonitrile resin has a high storage modulus and glass transition temperature (Tg). The water uptake is about 3% by weight after submersion in boiling water for 50 hours. The influence of curing processes on thermal stability and flame retardancy was also explored.
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U2 - 10.1039/c3ra46638h
DO - 10.1039/c3ra46638h
M3 - Article
AN - SCOPUS:84893189167
SN - 2046-2069
VL - 4
SP - 8383
EP - 8390
JO - RSC Advances
JF - RSC Advances
IS - 16
ER -