Improving the Intrinsic Viscosity of Waste Polyester Fabrics via Controlled Micro-Glycolysis and Self-Polycondensation

Polyethylene terephthalate (PET) plays a pivotal role in the chemical fiber industry, constituting over 50% of fiber consumption. However, the reduction of the recycled fiber-derived viscosity of the PET significantly impacts its spinning performance and restricts its closed-loop recycling to high-value regenerated fibers. To address these limitations, this study explored the viscosity improvement of black and white waste fiber-derived polyester particles through a two-step process involving micro-glycolysis and self-polycondensation. Initially, a continuous micro-glycolysis of fiber-derived PET was carried out in a twin-screw extruder with ethylene glycol (EG), which effectively cleaves the ester bonds in the PET chains, generating oligomers with reactive hydroxyl end groups. Subsequently, these oligomers were repolymerized without purification, and a higher molecular weight regenerated PET with enhanced intrinsic viscosity was obtained with antimony ethylene glycolate (Sb-EG) as a catalyst. The results revealed that the intrinsic viscosity decreased exponentially with increasing EG dosage during glycolysis, reaching approximately 50% of the initial value at 0.2-2 phr EG dosages. Optimal viscosity enhancement was achieved at a polycondensation time of 1-3 h, resulting in improved thermal stability and reduced crystallization temperatures. Importantly, regenerated PET samples with EG dosages of ≤2 phr demonstrated intrinsic viscosities of about 0.70 dL/g, meeting the standard for spin-grade polyester fiber, which is used to produce regenerated polyester fibers. This recycling process is low cost, environmentally friendly, and easy to scale-up, contributing significantly to the development of industrial recycling of waste polyester fabrics.