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功能高分子学报:2011,24(1):-
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双(N-间乙炔基苯基邻苯二甲酰亚胺)醚改性苯乙炔基硅氧硼烷
(1.华东理工大学材料科学与工程学院,特种功能高分子材料及相关技术教育部重点实验室, 上海 200237;2.华东理工大学材料科学与工程学院,特种功能高分子材料及相关技术教育部重点实验室, 上海 200238;3.华东理工大学材料科学与工程学院,特种功能高分子材料及相关技术教育部重点实验室, 上海 200239)
Characterization of Phenylethynyl Siloxane Borane Modified with Di((N-m-Acetylenylphenyl) Phthalimide)Ether
(1.Key Laboratory of Specially Functional Polymeric Materials and Related Technology of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China;2.Key Laboratory of Specially Functional Polymeric Materials and Related Technology of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200238, China;3.Key Laboratory of Specially Functional Polymeric Materials and Related Technology of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200239, China)
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中文摘要: 用双(N-间乙炔基苯基邻苯二甲酰亚胺)醚(DAIE)改性苯乙炔基硅氧硼烷(PESB)制得复合材料基体树脂(PESB DAIE)。通过FT-IR、DSC和TG研究了PESB DAIE的固化反应及耐热性。将PESB DAIE与纤维复合制得复合材料,研究了该材料的耐热性、弯曲强度及断面形貌。研究结果表明,固化物在氮气气氛下质量损失5%时的温度(T5%)为576 °C,空气气氛下T5%为507 °C。复合材料在500 °C下放置10 min后质量保留率为97.0%,弯曲强度为176 MPa。
Abstract:Phenylethynyl siloxane borane (PESB) was modified with di((N-m-acetylenylphenyl) phthalimide) ether (DAIE) and used as the matrix resin of composite. The curing mechanism and heat resistance were studied with FT-IR, DSC and TG. The flexural strength, heat resistance and fracture surface of the composites were also studied. Results showed that the temperature of 5% weight loss (T5%) of the cured blends was 576 °C in nitrogen and 507 °C in air. The mass retention of the composites after placed in 500 °C environment for 10 min was 97.0%, and the flexural strength was 176 MPa.
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高万星,宋宁,倪礼忠.双(N-间乙炔基苯基邻苯二甲酰亚胺)醚改性苯乙炔基硅氧硼烷[J].功能高分子学报,2011,24(1):.
GAO Wan-xing,SONG Ning,NI Li-zhong.Characterization of Phenylethynyl Siloxane Borane Modified with Di((N-m-Acetylenylphenyl) Phthalimide)Ether[J].Journal of Functional Polymers,2011,24(1):.