摘要
针对环氧树脂基材料的自修复,选取四氢邻苯二甲酸二缩水甘油酯作为芯材,采用三聚氰胺-甲醛树脂为壁材,对其进行微胶囊化包裹.结果表明,制得的具有单囊结构的环氧树脂微胶囊,胶囊粒径较小(约6.7μm)、囊壁较薄(约0.2μm)、芯含量较高(83.2 wt%),囊壁内、外表面光滑致密,胶囊具有良好的密闭性和耐热性;在微胶囊化过程中,三聚氰胺-甲醛树脂的缩聚反应动力学起关键作用,芯材没有参与囊壁形成的交联反应;包裹后的芯材活性保持不变,胶囊被复合到材料过程中囊芯活性也保持不变;胶囊的强度较高,能承受与基体材料复合过程中的外力作用,且与基体材料间粘结良好,在裂纹形成过程中能够随基体同时开裂.
Microcracks are easily generated inside polymers and polymer composites during their service in structural applications. Development and coalescence of microcracks would bring about catastrophic failure of the materials and then reduce their lifetimes. Therefore, early sensing, diagnosis and repair of microcracks become necessary for removing the latent perils. In this context, the materials possessing self-healing function are ideal for long-term operation. Attempts have been made to develop solutions in this filed, among which the route based on microcapsulation seems to be promising. Self-repairing polymer composites containing microencapsulated healing agent have attracted more and more research interests. The present article analyzed the existing problems and proposed the criteria for manufacturing qualified microencapsulated healing agent. Accordingly, microcapsules containing epoxy resin were successfully fabricated by in situ polymerization in an oil-in-water emulsion with poly（melamine-formaldehyde） （PMF） as the shell material and high-activity low-viscosity diglycidyl tetrahydro-o-phthalate （DTP） as the core substance. The typical synthesis procedures are described below. About 50 g DTP wasadded into 250 mL aqueous solution of 2% styrene-maleic sodium （SMS） .The mixture was vigorously agitated by a homogenizer for 10 min at a selected rate and then two drops of 1-octanol were added to eliminate surface bubbles of the emulsion. The pre-condensate of 12.5 g melamine and 27.1 g formaldehyde was prepared at 70 - 75 ~C for 30 min, and the pH value of the solution was kept at about 9 - 10 by adding triethanolamine. Subsequently, the precondensate solution was added to the above emulsion with 450 r/min continuous mechanical stirring by a two-bladed stirring paddle while the pH value of the solution was adjusted by adding citric acid. Eventually, the reaction mixture was cooled down to room temperature. The resultant slurry was neutralized by 2 % sodium carbonate solution, and then diluted with deionized water. The deposit of microcapsules was separated through a Buchner funnel and rinsed with deionized water and then vacuum dried. The synthesis method was improved by optimizing the processing parameters. The appropriate reaction time was about 30 - 60 min. Further extension of time had little influence on the products. The reaction temperature should be set at about 50 -70℃. The pH value of about 3.2 was appropriate and had complex effect on the properties of the products. The appropriate core/shell mass ratio was about 2 ： 1 - 3 ： 1. The size and size distribution of microcapsules were mainly determined by the dispersion rate and the emulsifier content. Having been encapsulated, the core material DTP kept the same activity as its raw version. The microcapsules＇ shell wall was relatively thin （ca. 0.2 μm）, which assured sufficient core content （83.2 wt%） even if the microcapsules were very small （ ca. 6.7 μm）. Moreover, the microcapsules were proved to be strong enough to survive handling during manufacturing self-healing composites. Having been pre-embedded in cured epoxy, the microcapsules had satisfied affinity to the matrix. They can be readily ruptured releasing DTP fluid as expected upon damaging of the composite, and activity of the released core material was the same as the raw material. Besides, the microcapsules had good sealing ability and high stability. They can be stored at room temperature for long time and could bear moderate or high temperatures applied for curing composites. The present work provided a new simple approach for mass-production of epoxy loaded microcapsules, which can be used to manufactui＇e self-healing composites or other self-curing stuffs like single constituent epoxy adhesive and self-locking threaded fasteners.
出处
《高分子学报》
SCIE
CAS
CSCD
北大核心
2008年第5期472-480,共9页
Acta Polymerica Sinica
基金
国家自然科学基金(基金号50573093
U0634001)资助项目
关键词
自修复
环氧树脂
三聚氰胺-甲醛
微胶囊
Self-repairing, Epoxy resin, Poly（melamine-formaldenhyde）, Microcapsule
