Yu Sizhu, Li Xiaodong, Zou Meishuai, Li Zhiren, Wang Shuo, Wang Danhui
School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, China.
Polymers (Basel). 2020 Aug 3;12(8):1732. doi: 10.3390/polym12081732.
In order to synthesize a new kind of buoyancy material with high-strength, low-density and low-water-absorption and to study the curing reaction of tetraglycidylamine epoxy resin with an aromatic amine curing agent, the non-isothermal differential scanning calorimeter (DSC) method is used to calculate the curing kinetics parameters of N,N,N',N'-tetraepoxypropyl-4,4'-diaminodiphenylmethane epoxy resin (AG-80) and the m-xylylenediamine (m-XDA) curing process. Further, buoyancy materials with different volume fractions of hollow glass microsphere (HGM) compounded with a AG-80 epoxy resin matrix were prepared and characterized. The curing kinetics calculation results show that, for the curing reaction of the AG-80/m-XDA system, the apparent activation energy increases with the conversion rates increasing and the reaction model is the Jander equation (three-dimensional diffusion, 3D, n = 1/2). The experimental results show that the density, compressive strength, saturated water absorption and water absorption rate of the composite with 55 v % HGM are 0.668 g·cm, 107.07 MPa, 0.17% and 0.025 h, respectively. This kind of composite can probably be used as a deep-sea buoyancy material.
为了合成一种高强度、低密度、低吸水率的新型浮力材料,并研究四缩水甘油胺环氧树脂与芳香胺固化剂的固化反应,采用非等温差示扫描量热法(DSC)计算N,N,N',N'-四环氧丙基-4,4'-二氨基二苯甲烷环氧树脂(AG-80)与间苯二甲胺(m-XDA)固化过程的固化动力学参数。此外,制备并表征了不同体积分数空心玻璃微珠(HGM)与AG-80环氧树脂基体复合的浮力材料。固化动力学计算结果表明,对于AG-80/m-XDA体系的固化反应,表观活化能随转化率的增加而增大,反应模型为扬德方程(三维扩散,3D,n = 1/2)。实验结果表明,HGM体积分数为55 v%的复合材料的密度、抗压强度、饱和吸水率和吸水速率分别为0.668 g·cm、107.07 MPa、0.17%和0.025 h。这种复合材料有望用作深海浮力材料。