PDF (2468K)
摘要
采用双酚A型环氧树脂(EP)和尼龙12微球(Nylon12)制备了EP/Nylon12复合材料。通过动态热机械分析仪(DMA)测试纯EP和EP/Nylon12复合材料储能模量和玻璃化转变温度(Tg)。在万能材料实验机上对试样进行拉伸测试和三点弯曲测试。采用扫描电镜(SEM)观察单缺口三点弯曲(SEN-3PB)测试样条断面微观形貌。结果表明,与纯EP相比,EP/Nylon12复合材料的拉伸强度随Nylon12微球用量增大而逐渐减小,杨氏模量变化不大,但断裂韧性和临界应变释放能均有明显提高,Nylon12微球用量为10%(wt,质量分数)制得的EP/Nylon12复合材料的玻璃化转变温度(Tg)为193.0℃,具有较好的热学性能,且力学性能得到提高,拉伸强度达到57.2MPa,杨氏模量达到2.50GPa,断裂韧性达到1.25MPa/m2,临界应变释放能达到548.4J/m2;Nylon12微球在EP中的增韧机理主要为微球与基体脱粘和裂纹偏转。
Abstract
EP/Nylon12 composites were prepared based on bisphenol-A type epoxy (EP) and Nylon12 microspheres.The storage modulus and glass transition temperature (Tg) of pure EP and EP/Nylon12 were tested by dynamic thermomechanical analyzer (DMA).Tensile and three-point bending test were carried out on a universal material testing machine.The microscopic morphologies of cross section of samples obtained from the single notch three points bending (SEN-3PB) test were observed through scanning electron microscopy (SEM).The results showed that the tensile strength of EP/Nylon12 decreased gradually with the increased loading of Nylon12 microspheres.Nylon12 microspheres had little influence on the storage modulus of EP.However,the fracture toughness (KIC) and the fracture energy (GIC) of EP/Nylon12 were improved significantly compared with pure EP.The glass transition temperature (Tg) of EP/Nylon12-10% was 193.0℃,it was with good thermal properties.Meanwhile,the mechanical properties were improved.Tensile strength,Young's modulus,KIC and GIC were increased to 57.2MPa,2.50GPa,1.25MPa/m2 and 548.4J/m2,respectively.The toughening mechanism of Nylon12 microspheres in EP were mainly de-bonding and crack deflection induced by microspheres.
关键词
尼龙12微球
/
环氧树脂
/
增韧
/
力学性能
/
三点弯曲
Key words
Nylon12 microsphere
/
epoxy resin
/
toughening
/
mechanical property
/
three-point bending
尼龙12微球增韧改性环氧树脂的研究[J].
化工新型材料, 2018, 46(11): 100-103 DOI:
[1] 吕晓雪,蒋敏,胡建冬,等.增韧改性环氧树脂及其复合材料的研制[J].化工新型材料,2015,43(11):79-81.
[2] Sprenger S.Improving mechanical properties of fiber-reinforced composites based on epoxy resins containing industrial surface-modified silica nanoparticles:review and outlook[J].Journal of Compossite Materials,2015,49(1):53-63.
[3] 吴俊青,俞科静,钱坤.碳纳米杂化材料的制备及其对环氧树脂性能的性能[J].化工新型材料,2016,44(8):41-43.
[4] Luo L J,Meng Y,Qiu T,et al.An epoxy-ended hyperbranched polymer as a new modifier for toughening and reinforcing in epoxy resin[J].Journal of Applied Polymer Science,2013,130(130):1064-1073.
[5] 胡传群,万式青.环氧树脂增韧技术进展[J].化工新型材料,2017,45(1):4-6.
[6] Rosso P,Ye L,Friedrich K,et al.A toughened epoxy resin by silica nanoparticle reinforcement[J].Journal of Applied Polymer Science,2006,100(3):1849-1855.
[7] Sprenger S,Kothmann M H,Altstaedt V.Carbon fiber-reinforced composites using an epoxy resin matrix modified with reactive liquid rubber and silica nanoparticles[J].Composites Science and Technology,2014,105:86-95.
[8] Bucknall C B,Cilbert A H.Toughening tetrafunctional epoxy resins using polyetherimide[J].Polymer,1989,30(2):213-217.
[9] Carfagna C,Nicolais L,Amendola E,et.al.Toughening epoxy resin by liquid crystalline polymers[J].Journal of Applied Polymer Science,2010,44(44):1465-1471.
[10] 单书燕,程品潇,于晓燕,等.超细二氧化硅微粉增韧改性环氧树脂的研究[J].胶体与聚合物,2016,34(1):7-9.
[11] Liu J,Sue H J,Thompson Z J,et al.Nanocavitation in self-assembled amphiphilic block copolymer-modified epoxy[J].Macromolecule,2008,41(20):7616-7624.
[12] Pavan A.Determination of fracture toughness (GIC and KIC) at moderately high loading rates[J].European Structural Integrity Society,2001,28(1):27-58.
[13] 赵春霞,周俊萍,曾凯,等.尼龙12微球在苯并噁嗪树脂中的增韧机理[J].高分子材料科学与工程,2017,33(1):63-67.
[14] 王暖,李超芹.ACM/PA12热塑性弹性体的制备及性能研究[J].塑料工业,2016,44(6):12-16.
基金资助
西南石油大学培育项目(2014PYZ013);西南石油大学大学生开放实验重点项目(KSZ16114)