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柔性缓冲层对T300/BADCy复合材料力学性能影响研究
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作者 任鹏刚 梁国正 +3 位作者 杨洁颖 王结良 房红强 张增平 《航空材料学报》 EI CAS CSCD 2004年第4期35-38,共4页
为增强T300/BADCy复合材料的界面性能,用E51环氧树脂/丙酮溶液对T300纤维进行表面处理,在T300/BADCy复合材料界面处能形成柔性的口恶唑啉酮五元环缓冲层。利用红外光谱法研究环氧树脂与氰酸酯树脂的反应机理,并比较不同浓度E51环氧树脂... 为增强T300/BADCy复合材料的界面性能,用E51环氧树脂/丙酮溶液对T300纤维进行表面处理,在T300/BADCy复合材料界面处能形成柔性的口恶唑啉酮五元环缓冲层。利用红外光谱法研究环氧树脂与氰酸酯树脂的反应机理,并比较不同浓度E51环氧树脂处理液对复合材料力学性能的影响,发现经5wt%浓度的E51环氧液处理的T300/BADCy复合材料层间剪切强度提高了16%,弯曲强度提高了4%,当处理液的浓度大于5wt%时,T300/BADCy复合材料的力学性能有所下降。采用扫描电镜研究处理前、后T300/BADCy复合材料层间剪切断口形貌,发现未处理的T300/BADCy树脂复合材料断口的界面处存在明显裂纹,处理后的复合材料界面没有裂纹,且断裂主要发生在树脂基体内部。 展开更多
关键词 柔性缓冲层 T300/badcy复合材料 力学性能 树脂基复合材料 双酚A型二氰酸酯
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PT/BADCy/PASF三元树脂体系耐热性能的研究
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作者 崔宝军 陈维君 +4 位作者 李刚 宋军军 耿庆生 梁泰硕 王文博 《化学与粘合》 CAS 2013年第6期1-4,共4页
首先研究了PT/BADCy二元树脂体系的力学性能和耐热性能,结果表明:BADCy的加入可以改善PT树脂韧性,体系中PT树脂比例越高,灼烧后混合树脂的残留率越高。还重点研究了PT/BADCy/PASF三元树脂体系,力学分析表明:PASF的加入,大大提高了体系... 首先研究了PT/BADCy二元树脂体系的力学性能和耐热性能,结果表明:BADCy的加入可以改善PT树脂韧性,体系中PT树脂比例越高,灼烧后混合树脂的残留率越高。还重点研究了PT/BADCy/PASF三元树脂体系,力学分析表明:PASF的加入,大大提高了体系的韧性,当含量为10%wt时,常温、200℃以及300℃剪切强度分别为20.88、22.78、14.36MPa,90°常温剥离强度为26.89N/cm。热学分析表明:不同含量PASF的三元树脂体系的热降解趋势基本一致,高温灼烧后残留率大致相同。PASF树脂的耐热性、耐灼烧型与PT/BADCy相当,三者可以实现理想匹配。 展开更多
关键词 酚醛型氰酸酯(PT) 双酚A型氰酸酯低聚物(badcy) 端羟基聚芳砜(PASF) 韧性 耐热性
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CTBN改性双酚A型氰酸酯树脂的性能 被引量:10
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作者 任鹏刚 梁国正 杨洁颖 《材料研究学报》 EI CAS CSCD 北大核心 2005年第4期443-448,共6页
为改善氰酸酯树脂的冲击韧性,在双酚A型二氰酸酯(BADCy)树脂中混入了不同含量的端羧基丁腈橡胶(CTBN).用差示扫描量热法(DSC)及红外光谱法(FTIR)对CTNB/BADCy共混体系的反应性研究发现,CTBN能促进BADCy低温下的三嗪环反应,但是使BADCy... 为改善氰酸酯树脂的冲击韧性,在双酚A型二氰酸酯(BADCy)树脂中混入了不同含量的端羧基丁腈橡胶(CTBN).用差示扫描量热法(DSC)及红外光谱法(FTIR)对CTNB/BADCy共混体系的反应性研究发现,CTBN能促进BADCy低温下的三嗪环反应,但是使BADCy的后处理温度提高.SEM分析表明,当CTBN的含量(质量分数)大于15%后,有CTBN颗粒从BADCy中析出,形成两相结构,且随着CTBN含量的增大,分散相的粒径增大,在断口处产生的银纹和剪切带使BADCy/CTBN共混体系的韧性提高.当CTBN的含量为25%时体系的冲击强度提高了2.3倍. 展开更多
关键词 有机高分于材料 弹性体 增韧 CTBN badcy
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聚乙烯基吡咯烷酮改性氰酸酯树脂耐湿热性能研究 被引量:1
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作者 王结良 梁国正 +2 位作者 赵雯 吕生华 马晓燕 《航空材料学报》 EI CAS CSCD 2006年第6期72-76,共5页
对聚乙烯基吡咯烷酮(PVP)/氰酸酯树脂体系的耐湿热性能进行系统研究。选取湿热老化环境为100h/100℃沸水老化。结果表明,随着体系中PVP用量的增大,固化改性树脂的吸湿率逐渐增大。湿热老化使固化树脂的力学性能急剧下降,但PVP的加入能... 对聚乙烯基吡咯烷酮(PVP)/氰酸酯树脂体系的耐湿热性能进行系统研究。选取湿热老化环境为100h/100℃沸水老化。结果表明,随着体系中PVP用量的增大,固化改性树脂的吸湿率逐渐增大。湿热老化使固化树脂的力学性能急剧下降,但PVP的加入能够有效改善下降趋势。当PVP用量为5wt%时,湿热老化后固化树脂的弯曲强度和冲击强度的强度保持率从原始氰酸酯的38.8%和35.5%提高到86.8%和66.1%。湿热老化对体系力学性能的损伤可从固化树脂老化前后断口形貌得到合理解释。湿热老化过程中,PVP的加入对体系的热性能、电性能及尺寸稳定性的不利影响较小。综合考虑体系的各项性能指标,以PVP用量为5%时体系耐湿热性能最佳。 展开更多
关键词 聚乙烯基吡咯烷酮(PVP) 双酚A型氰酸酯树脂(badcy) 湿热性能
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PBO fibers/fluorine-containing liquid crystal compound modified cyanate ester wave-transparent laminated composites with excellent mechanical and flame retardance properties 被引量:5
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作者 Zheng Liu Xiaoli Fan +4 位作者 Junliang Zhang Lixin Chen Yusheng Tang Jie Kong Junwei Gu 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2023年第21期16-29,共14页
Bisphenol A dicyanate ester resins modified by fluorine-containing liquid crystal compound(LCFE)are applied as polymer matrix(LCFE-BADCy),poly(p-phenylene-2,6-benzobisoxazole)(PBO)fibers as rein-forcements,and fluorin... Bisphenol A dicyanate ester resins modified by fluorine-containing liquid crystal compound(LCFE)are applied as polymer matrix(LCFE-BADCy),poly(p-phenylene-2,6-benzobisoxazole)(PBO)fibers as rein-forcements,and fluorine/adamantane PBO precursor(pre FABPBO)as interfacial compatibilizer to prepare the corresponding PBO fibers/FABPBO/LCFE-BADCy wave-transparent laminated composites.LCFE could improve the order degree of BADCy cured network,in favor of enhancing the wave-transparent perfor-mance,mechanical properties,and intrinsic thermal conductivity.The dielectric constant and dielectric loss of PBO fibers/FABPBO/LCFE-BADCy composites are highly temperature(25–200℃)and frequency(10^(4)–10^(7) Hz and 8.2–12.4 GHz)stable with the value of 2.49 and 0.003 under 10^(6) Hz at 25℃,and the corresponding wave transmission efficiency is 95.0%,higher than that of 92.5%for PBO fibers/BADCy com-posites.The interlamellar shear strength and flexural strength are respectively 50.7 MPa and 682.5 MPa,38.1%and 16.2%higher than those of PBO fibers/BADCy composites.Besides,the volume resistivity,breakdown voltage,heat resistance index,glass transition temperature,flame retardant grade,and ul-timate oxygen index of PBO fibers/FABPBO/LCFE-BADCy composites are respectively 5.3×10^(15)Ωcm,29.75 kV/mm,217.2℃,245.7℃,V-1 grade,and 33.6%,expected to be performed as a new generation of“lightweight/loading/wave-transparent”electromagnetic window materials in advanced military weapons and civil communication base station. 展开更多
关键词 Bisphenol A dicyanate ester(badcy)resins Fluorine-containing liquid crystal compound Poly(p-phenylene-2 6-benzobisoxazole) (PBO)fibers Fluorine/adamantane PBO precursor Wave-transparent laminated composites
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Block copolymer functionalized quartz fibers/cyanate ester wave-transparent laminated composites
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作者 Jiani Zhang Zheng Liu +3 位作者 Muyi Han Junliang Zhang Yusheng Tang Junwei Gu 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2023年第8期189-197,共9页
A block copolymer of PDMS-b-PGMA is synthesized by polymerizing glycidyl methacrylate(GMA)via reversible addition-fragmentation chain transfer(RAFT)polymerization applying a polydimethylsiloxane(PDMS)based macro-RAFT ... A block copolymer of PDMS-b-PGMA is synthesized by polymerizing glycidyl methacrylate(GMA)via reversible addition-fragmentation chain transfer(RAFT)polymerization applying a polydimethylsiloxane(PDMS)based macro-RAFT agent,which is then performed to functionalize the quartz fibers(QFs@PDMS-b-PGMA)via a simple coating process.Finally,the QFs@PDMS-b-PGMA/bisphenol A dicyanate ester(BADCy)wave-transparent laminated composites are fabricated by high-temperature molding.Nuclear magnetic resonance(NMR)spectroscopy,Fourier transform infrared(FT-IR)spectroscopy and size ex-clusion chromatography(SEC)demonstrate the successful preparation of PDMS-b-PGMA with expected structure.When the molar mass and coating amount of PDMS-b-PGMA are respectively 8100 g/mol and 2.0 wt.%,QFs@PDMS-b-PGMA/BADCy wave-transparent laminated composites present optimal mechan-ical properties and wave-transparent performance.The interlaminar shear strength(ILSS)and flexural strength are 53.6 and 552.0 MPa,respectively.Meanwhile,the dielectric constant and dielectric loss val-ues are 2.61 and 0.0028 at 1 MHz(wave transmittance of 93.8%),showing good stability at different frequencies(102-106 Hz and 8.4-12.4 GHz)and temperatures(25-250℃). 展开更多
关键词 Bisphenol A dicyanate ester(badcy)resins Quartz fibers(QFs) Wave-transparent laminated composites Block copolymer
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氰酸酯预聚物/聚砜共混树脂的制备及其性能研究 被引量:3
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作者 崔宝军 陈维君 +3 位作者 宋军军 李刚 耿庆生 梁泰硕 《化学与粘合》 CAS 2016年第1期4-7,53,共5页
提供了一种制备氰酸酯预聚物/聚砜共混树脂的工艺,该工艺过程平稳、温和、易控制。通过红外光谱IR研究,随着反应时间的延长,-OCN的红外特征吸收峰变弱,triazine特征吸收峰明显增强。随着PSF/BADCy比值提高,共混树脂的常温剪切强度相应增... 提供了一种制备氰酸酯预聚物/聚砜共混树脂的工艺,该工艺过程平稳、温和、易控制。通过红外光谱IR研究,随着反应时间的延长,-OCN的红外特征吸收峰变弱,triazine特征吸收峰明显增强。随着PSF/BADCy比值提高,共混树脂的常温剪切强度相应增加;低含量的PSF对树脂高温(230℃)强度影响不大,高含量时,高温剪切强度降低明显。通过DMA分析,共混物只体现出BADCy相关的Tg值,BADCy预聚物和PSF树脂事实上形成一种互穿网络结构(IPN)。共混树脂的真实Tg值为230℃左右。E′-T关系表明,只有高含量的PSF才对BADCy有明显的增韧作用。Tanδ~T关系表明,Tanδ=0.02,总体上共混树脂的韧性不高。通过TG分析,共混树脂的初始分解温度达到400℃,是一种优异的耐高温材料,共混树脂的失重过程完全遵从BADCy自身的热氧化分解规律。 展开更多
关键词 氰酸酯预聚物 聚砜 共混树脂 PSF/badcy比值 互穿网络结构 耐高温材料
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Random copolymer membrane coated PBO fibers with significantly improved interfacial adhesion for PBO fibers/cyanate ester composites 被引量:8
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作者 Lin TANG Junliang ZHANG Junwei GU 《Chinese Journal of Aeronautics》 SCIE EI CAS CSCD 2021年第2期659-668,共10页
Poly(p-phenylene-2,6-benzobisoxazole)(PBO) fibers possess excellent dielectric, mechanical properties and heat resistance. However, the surface of PBO fibers is smooth and highly chemical inert, resulting in poor inte... Poly(p-phenylene-2,6-benzobisoxazole)(PBO) fibers possess excellent dielectric, mechanical properties and heat resistance. However, the surface of PBO fibers is smooth and highly chemical inert, resulting in poor interfacial compatibility to polymer matrix, which severely limits its wider application in high-performance fiber-reinforced resin matrix composites. In this work, random copolymers(P(S-co-BCB-co-MMA)) containing benzocyclobutene in the side-chain were synthesized by reversible addition-fragmentation chain transfer(RAFT) polymerization, which were then utilized to form dense random copolymer membrane on the surface of PBO fibers by thermally cross-linking at 250 °C(PBO@P fibers). Four kinds of synthesized P(S-co-BCB-co-MMA) with different number-average molar mass(Mn) were well controlled and possessed narrow dispersity.When the Mnwas 32300, the surface roughness of PBO@P fibers was increased from 11 nm(PBO fibers) to 39 nm. In addition, PBO@P fibers presented the optimal interfacial compatibility with bisphenol A cyanate(BADCy) resins. And the single fiber pull-out strength of PBO@P fibers/BADCy micro-composites was 4.5 MPa, increasing by 45.2% in comparison with that of PBO fibers/BADCy micro-composites(3.1 MPa). Meantime, PBO@P fibers still retained excellent tensile strength(about 5.1 GPa). Overall, this work illustrates a simple and efficient surface functionalization method, which would provide a strong theoretical basis and technical support for controlling the surface structure & chemistry of inert substrates. 展开更多
关键词 RAFT polymerization MEMBRANE PBO fibers Bisphenol A cyanate(badcy)resins Interfacial adhesion
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