Open Access Article
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Scalable Glycolysis-Based Depolymerization of Polyurethane Foam Wastes Enabled by Ionic Liquids

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Francisco Velasco , Rocio Villa , Nicolas Alonso , Rebeca Salas , Jairton Dupont , Eduardo Garcia-Verdugo and Pedro Lozano

Received 15th July 2025 , Accepted 29th September 2025

First published on 1st October 2025


Abstract

We report a sustainable and scalable strategy for the chemical depolymerization of polyurethane foam waste (PUFW), employing the ionic liquids (ILs) 1-n-butyl-3-methylimidazolium chloride ([Bmim][Cl]) and 1-n-butyl-3-methylimidazolium acetate ([Bmim][OAc]) as dual-function systems that act both as reactive media and as efficient catalysts for the selective glycolysis of urethane bonds. Full depolymerization of PUFW is achieved under mild conditions (<100 °C, 1 atm) within 4-5 hours, offering a scalable alternative (up to 100 g of PUFW processing capability) to conventional glycolysis methods that typically require harsh thermal conditions (180–250 °C). The addition of water to the reaction medium enables the direct precipitation of the recycled polyol and allows for the efficient recovery and reuse of the water-miscible ILs [Bmim][Cl] and [Bmim][OAc], enhancing the sustainability of the process The recycled product is then washed, dried, and analyzed by means of solubility test in dimethyl sulfoxide (DMSO), hydroxyl index (iKOH) value, nuclear magnetic resonance (NMR), and attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. Finally, the obtained recycled polyol is homogenized with the virgin polyol to synthesize new flexible polyurethane foams (FPUFs) that display identical physico-chemical and mechanical properties as the original FPUF. It should be noted that this glycolytic depolymerization process does not generate waste, since the complete mixture of reaction products is suitable for reuse as starting material in the synthesis of new FPUFs. The active depolymerization medium is completely recoverable and reusable, proving its operational stability for up to six consecutive cycles and promoting the “greenness” of the process. Noteworthy, the effectiveness of this process is also demonstrated for the case of the recalcitrant rigid PUFs (RPUFs), namely as polyisocyanurate (PIR), not only pushing towards the versatility of this process, but also its potential application on an industrial scale


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