Aksit Alper, Menzel Teresa, Aksit Merve, Altstädt Volker
Department of Polymer Engineering, University of Bayreuth, Universitätsstraße 30, 95447 Bayreuth, Germany.
Bavarian Polymer Institute and Bayreuth Institute of Macromolecular Research, University of Bayreuth, Universitätsstraße 30, 95447 Bayreuth, Germany.
Materials (Basel). 2020 Mar 9;13(5):1237. doi: 10.3390/ma13051237.
Polyamide 66 (PA66)/poly (2,6-dimethyl-1,4-phenylene ether) (PPE) blends with a ratio of 50/50 (w/w) were produced by a twin-screw compounder. The immiscible blends were compatibilized using two different styrene-maleic anhydride copolymers (SMA) with a low (SMA) and a high (SMA) maleic anhydride (MA) concentration of 8 and 25 wt%, respectively. Furthermore, the SMA content was varied from 0 to 10 wt%. The influence of MA concentration and SMA content on the morphological and thermomechanical properties of PA66/PPE blends was investigated. Herein, we established correlations between the interfacial activity of the SMA with blend morphology and corresponding tensile properties. A droplet-sea to co-continuous morphology transition was shown by scanning electron microscopy to occur between 1.25 and 5 wt% in the case of SMA. For SMA, the transition started from 7.5 wt% and was still ongoing at 10 wt%. It was found that SMA with 10 wt% content enhanced the tensile strength (10%) and elongation at break (70%) of PA66/PPE blends. This improvement can be explained by the strong interfacial interaction of SMA within the blend system, which features the formation of nanoemulsion morphology, as shown by transmission electron microscopy. Very small interdomain distances hinder matrix deformations, which forces debonding and cohesive failure of the PPE phase as a "weaker" main deformation mechanism. Due to a lack of interfacial activity, the mechanical properties of the blends with SMA were not improved.
通过双螺杆混炼机生产了比例为50/50(重量/重量)的聚酰胺66(PA66)/聚(2,6-二甲基-1,4-亚苯基醚)(PPE)共混物。使用两种不同的苯乙烯-马来酸酐共聚物(SMA)对不相容的共混物进行增容,其中一种SMA的马来酸酐(MA)浓度较低(8重量%),另一种SMA的MA浓度较高(25重量%)。此外,SMA的含量在0至10重量%之间变化。研究了MA浓度和SMA含量对PA66/PPE共混物的形态和热机械性能的影响。在此,我们建立了SMA的界面活性与共混物形态及相应拉伸性能之间的相关性。扫描电子显微镜显示,对于SMA,在1.25至5重量%之间发生了从液滴-海相到共连续形态的转变。对于另一种SMA,转变从7.5重量%开始,在10重量%时仍在进行。发现含有10重量%SMA的PA66/PPE共混物的拉伸强度提高了10%,断裂伸长率提高了70%。这种改善可以通过SMA在共混体系中的强界面相互作用来解释,透射电子显微镜显示其特征是形成了纳米乳液形态。非常小的相间距阻碍了基体变形,这迫使作为“较弱”主要变形机制的PPE相发生脱粘和内聚破坏。由于缺乏界面活性,含有SMA的共混物的机械性能没有得到改善。