Mechanical Properties of Composite Materials from Waste Poly(ethylene terephthalate) Reinforced with Glass Fibers and Waste Window Glass

Abstract

After primary uses of the plastic product, most developing countries like Ethiopia are facing a shortage of postconsumer disposal waste sites and it became a very serious problem on environmental pollution due to its nonbiodegradable nature. For this reason, regenerating and using the waste product as resources and reducing environmental pollutions are a great opportunity. This research is aimed at the manufacturing of composite materials from waste poly(ethylene terephthalate) (PET) bottles reinforced with glass fibers and filled with waste glass powder for floor tile applications. The tile composites were prepared by the melt-mixing method followed by compression molding. The effect of filler, fiber, and PET matrix loading on the composite was investigated using their tensile, compression, and flexural strength tests. The sample was characterized using a universal testing machine. PerkinElmer FTIR instrument was also used. For this, eleven samples prepared by varying the glass fiber weight % from 0 to 10, PET matrix weight % from 70 to 85, and glass powder filler weight % from 5 to 20. The measurement results of the composite were maximum tensile strength (81.625 MPa) and flexural strength (1067.59 MPa) recorded at 10%weight of glass fiber, 85% weight of PET matrix, and 5%weight of window glass filler. The maximum compressive strength is 1876.14 MPa at 10% weight glass fiber, 70 wt% PET matrix, and 20 wt% window glass filler. Based on this, the tensile strength and flexural strength increased with increased weight % of glass fiber and decreased with increased window glass filler. The FTIR spectrum shows some of the groups that have been removed from the recycled PET; this explains the brittleness of the recycled PET as compared to the waste bottle PET. The microstructure was uniformly distributed, and the material became opaque, probably because the decrease in chain length improves chain packing, increasing the crystallinity degree and crystal size.