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Investigation of structure property relationships in liquid processible, solvent free, thermally stable bismaleimide-triazine (BT) resins

机译:液体可加工,无溶剂,热稳定的双马来酰亚胺-三嗪(BT)树脂中结构性质关系的研究

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摘要

Three cyanate ester monomer or oligomer species: 2,2-bis(4-cyanatophenyl)propane 1, 1-1-bis(4-cyanatophenyl)ethane (2), and the oligomeric phenolic cyanate (PrimasetTM PT30) (3), are blended in various ratios with bis(4-maleimidophenyl)methane, (4), to form binary and ternary mixtures (11 in total) and cured, in the absence of catalysts (3 K/min to 150 °C + 1 hour; 3 K/min to 200 °C + 3 hours), followed by a post cure (3 K/min to 260 °C + 1 hour). The use of liquid monomer, (2), offers the possibility of liquid processing in blends containing minority compositions of bismaleimide. Glycidylmethacrylate is explored as a reactive diluent (2.5-10 wt %) to linked interpenetrating network polymer structures comprising cyanate ester and bismaleimide components with glass transition temperatures of 267-275 ºC, depending on composition; the onset of thermo-oxidative degradation ranges from 386-397 ºC. When a binary blend of (2) and (3) (with the former in the minority) is co-cured with (4), an excellent balance of properties is achieved with liquid processing, a Tg greater than 400 C and onset of degradation of 425 ºC in static air. Kinetic analysis of DSC data using Ozawa and Kissinger methods yield activation energies of between 107- 112 kJ/mole for a binary blend of (1)90-(4)10, which is in good agreement with literature. Molecular dynamics simulation of the same blend in cured form gave a simulated glass transition temperature of 250 C that is in very close agreement with empirical DMTA data.
机译:三种氰酸酯单体或低聚物种类:2,2-双(4-氰基苯基)丙烷1,1-1-双(4-氰基苯基)乙烷(2)和低聚酚醛氰酸酯(PrimasetTM PT30)(3)与双(4-马来酰亚胺基苯基)甲烷以各种比例混合(4),形成二元和三元混合物(共11种)并在没有催化剂的情况下固化(3 K / min至150°C + 1小时; 3) K / min至200°C + 3小时),然后进行后固化(3 K / min至260°C + 1小时)。液体单体(2)的使用提供了在含有双马来酰亚胺的少数组成的共混物中进行液体加工的可能性。甲基丙烯酸缩水甘油酯作为一种活性稀释剂(2.5-10重量%)被研究用于连接的互穿网络聚合物结构,该结构包含氰酸酯和双马来酰亚胺组分,取决于组成,其玻璃化转变温度为267-275ºC;热氧化降解的起始温度为386-397ºC。当(2)和(3)的二元共混物(前者为少数)与(4)共固化时,通过液体加工,Tg大于400C并开始出现液体,可以实现优异的性能平衡。在静态空气中降解425ºC。使用Ozawa和Kissinger方法对DSC数据进行动力学分析,得出(1)90-(4)10的二元共混物的活化能在107-112 kJ / mol之间,这与文献资料非常吻合。固化形式的相同共混物的分子动力学模拟给出了250C的模拟玻璃化转变温度,与DMTA经验数据非常接近。

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