Kargarfard Neda, Diedrich Norman, Rupp Harald, Döhler Diana, Binder Wolfgang H
Faculty of Natural Science II, Martin Luther University Halle-Wittenberg, Von-Danckelmann-Platz 4, D-06120 Halle (Saale), Germany.
Leibniz-Institut für Polymerforschung Dresden e. V., Abteilung Reaktive Verarbeitung, Hohe Str. 6, D-01069 Dresden, Germany.
Polymers (Basel). 2017 Dec 24;10(1):17. doi: 10.3390/polym10010017.
Investigation of the curing kinetics of crosslinking reactions and the development of optimized catalyst systems is of importance for the preparation of self-healing nanocomposites, able to significantly extend their service lifetimes. Here we study different modified low molecular weight multivalent azides for a capsule-based self-healing approach, where self-healing is mediated by graphene-supported copper-nanoparticles, able to trigger "click"-based crosslinking of trivalent azides and alkynes. When monitoring the reaction kinetics of the curing reaction via reactive dynamic scanning calorimetry (DSC), it was found that the "click-crosslinking" reactivity decreased with increasing chain length of the according azide. Additionally, we could show a remarkable "click" reactivity already at 0 °C, highlighting the potential of click-based self-healing approaches. Furthermore, we varied the reaction temperature during the preparation of our tailor-made graphene-based copper(I) catalyst to further optimize its catalytic activity. With the most active catalyst prepared at 700 °C and the optimized set-up of reactants on hand, we prepared capsule-based self-healing epoxy nanocomposites.
研究交联反应的固化动力学以及开发优化的催化剂体系对于制备能够显著延长其使用寿命的自修复纳米复合材料至关重要。在此,我们研究了用于基于胶囊的自修复方法的不同改性低分子量多价叠氮化物,其中自修复由石墨烯负载的铜纳米颗粒介导,能够引发三价叠氮化物和炔烃的“点击”交联。当通过反应性动态扫描量热法(DSC)监测固化反应的反应动力学时,发现“点击交联”反应性随相应叠氮化物链长的增加而降低。此外,我们能够在0°C时就显示出显著的“点击”反应性,突出了基于点击的自修复方法的潜力。此外,我们在制备定制的基于石墨烯的铜(I)催化剂过程中改变反应温度,以进一步优化其催化活性。利用在700°C制备的活性最高的催化剂以及手头优化的反应物设置,我们制备了基于胶囊的自修复环氧纳米复合材料。