Abstract
Elastane is ubiquitous in polyester-based textiles and complicates depolymerization-based recycling because it can undergo thermal degradation and chemical bond cleavage, consuming reagents and forming low-molecular by-products that may compromise monomer quality. Here, we investigate alkaline PET depolymerization of PET/elastane blends under an intentional base-competition scenario in a laboratory kneader. Pure PET (100/0) and PET/EL blends (95/5 and 85/15, wt/wt) were processed under quasi-solid-state conditions at 140 °C for 5 min using solid NaOH dosed at 2.1 mol per mol PET repeat unit and pelletized feedstocks to ensure scale-relevant mixing and reproducible chamber filling. Torque and bulk-temperature profiles were similar across compositions, and isolated terephthalic acid yields remained in a narrow corridor (68-71%), indicating that PET depolymerization is not measurably impaired by 5-15 wt% elastane within this reaction window. Differential scanning calorimetry of water-insoluble residues revealed pronounced changes in elastane-related thermal transitions, evidencing elastane modification during treatment. Targeted (1)H NMR screening of recovered TA against a 4,4'-methylenedianiline spiked reference showed no detectable co-isolated aromatic diamines. Overall, the study demonstrates robust monomer recovery from mixed PET/EL textiles under solid-NaOH, short-residence, solvent-lean processing, while identifying residue analytics as the key bottleneck for quantifying elastane fate and closing component balances.