Synthesis and properties of novel copolymers of poly(ether ketone ketone) and poly(ether sulfone ether ketone ketone) containing 1,4-naphthylene moieties

被引:9
|
作者
Liu, Limin [1 ]
Wang, Guixia [1 ]
Yan, Tao [1 ]
Cai, Mingzhong [1 ]
机构
[1] Jiangxi Normal Univ, Dept Chem, Nanchang 330022, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Poly(ether ketone ketone); 1; 4-naphthylene unit; Friedel-Crafts acylation; terephthaloyl chloride; copolymer; thermal property; PRECIPITATION POLYCONDENSATION; BLOCK-COPOLYMERS; MELTING BEHAVIOR; POLYMERIZATION; POLYKETONES; CHAIN; PEEK;
D O I
10.1177/0954008316685412
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A new monomer containing naphthalene and sulfone groups, 4,4'-bis(1-naphthoxy)diphenylsulfone (BNODPS), was easily prepared by the condensation reaction of 4,4'-dichlorodiphenylsulfone with 1-naphthol in the presence of base in dimethyl sulfoxide. Novel copolymers of poly(ether ketone ketone) and poly(ether sulfone ether ketone ketone) containing 1,4-naphthylene moieties were synthesized by the electrophilic Friedel-Crafts acylation copolycondensation of terephthaloyl chloride with a mixture of diphenyl ether (DPE) and BNODPS, over a wide range of DPE/BNODPS molar ratios, in the presence of anhydrous AlCl3 and N-methylpyrrolidone (NMP) in 1,2-dichloroethane. The polymers obtained were characterized by different physicochemical techniques. The copolymers with 5-25 mol% BNODPS are semicrystalline and had remarkably increased T(g)s and decreased T(m)s over the wholly para-linked poly(ether ketone ketone) due to the incorporation of bulky and rigid 1,4-naphthylene moieties and flexible sulfone linkages in the main chains. The copolymer VI with 25 mol% BNODPS had not only high T-g of 185 degrees C but also moderate T-m of 335 degrees C, having good potential for melt processing. The copolymer VI had tensile strength of 102.2 MPa, Young's modulus of 2.78 GPa, and elongation at break of 15.9% and exhibited high thermal stability and good resistance to organic solvents.
引用
收藏
页码:172 / 180
页数:9
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