Slezák Emese, Ronkay Ferenc, Réz Dávid, Bocz Katalin
Department of Organic Chemistry and Technology, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, Műegyetem rkp. 3., H-1111, Budapest, Hungary.
Department of Innovative Vehicles and Materials, GAMF Faculty of Engineering and Computer Science, John von Neumann University, H-6000, Kecskemét, Hungary.
Heliyon. 2024 May 29;10(11):e32096. doi: 10.1016/j.heliyon.2024.e32096. eCollection 2024 Jun 15.
Reprocessing potential of recycled poly(ethylene-terephthalate) (RPET)/ethylene-butyl-acrylate-glycidyl methacrylate (EBA-GMA) blends was investigated. PET flakes from food packaging were compounded with 0, 5, 10, 15 and 20 % EBA-GMA. Injection moulded specimens were produced, and some of the specimens were grinded, and reproduced to simulate real reprocessing. It was revealed by scanning electron microscopy that the distribution and particle size of the elastomer did not change notably after recycling. Noticeable degradation of the polymer matrix was observable after every processing step. Such deterioration of PET resulted in higher crystallinity and rigid amorphous fraction, as found by differential scanning calorimetry, which ultimately led to higher storage modulus, while the notched impact strength and elongation at break decreased. Nevertheless, the mechanical performance of the reprocessed RPET/EBA-GMA blends still significantly outperforms that of the neat PET recyclate. The degree of chain breakage was found to be the primary factor determining the recyclability of RPET/EBA-GMA blends.
研究了回收聚对苯二甲酸乙二酯(RPET)/乙烯-丁基丙烯酸酯-甲基丙烯酸缩水甘油酯(EBA-GMA)共混物的再加工潜力。将食品包装用的PET薄片与0%、5%、10%、15%和20%的EBA-GMA进行共混。制备注塑成型试样,将部分试样研磨并重新成型以模拟实际再加工过程。扫描电子显微镜显示,回收后弹性体的分布和粒径没有明显变化。在每个加工步骤后都可观察到聚合物基体有明显降解。差示扫描量热法表明,PET的这种劣化导致结晶度和刚性非晶部分增加,最终导致储能模量提高,而缺口冲击强度和断裂伸长率降低。尽管如此,再加工的RPET/EBA-GMA共混物的机械性能仍明显优于纯PET回收物。发现链断裂程度是决定RPET/EBA-GMA共混物可回收性的主要因素。