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Base- or acid-assisted polystyrene plastic degradation in supercritical CO2

Waste Disposal & Sustainable Energy 2023 16 citations

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Researchers demonstrated that polystyrene plastic can be chemically degraded in supercritical CO₂ at 400°C when assisted by base or acid solutions, finding the process converts PS into hydrogen-rich gases and could offer a feasible route for disposing of plastic waste.

Polymers

UNLABELLED: Plastic has caused serious "white pollution" to the environment, and the highly inert characteristics of plastic bring a major challenge for degradation. Supercritical fluids have unique physical properties and have been widely used in various fields. In this work, supercritical CO (Sc-CO) with mild conditions was selected and assisted by NaOH/HCl solution to degrade polystyrene (PS) plastic, and the reaction model was designed using response surface methodology (RSM). It was found that, regardless of the types of assistance solutions, the factors affecting PS degradation efficiencies were reaction temperature, reaction time, and NaOH/HCl concentration. At the temperature of 400 °C, time of 120 min, and base/acid concentration of 5% (in weight), 0.15 g PS produced 126.88/116.99±5 mL of gases with 74.18/62.78±5 mL of H, and consumed 81.2/71.5±5 mL of CO. Sc-CO created a homogeneous environment, which made PS highly dispersed and uniformly heated, thus promoting the degradation of PS. Moreover, Sc-CO also reacted with the degradation products to produce new CO and more CH and CH (=4, 6). Adding NaOH/HCl solution not only improved the solubility of PS in Sc-CO, but also provided a base/acid environment that reduced the activation energy of the reaction, and effectively improved the degradation efficiencies of PS. In short, degrading PS in Sc-CO is feasible, and better results are obtained with the assistance of base/acid solution, which can provide a reference for the disposal of waste plastics in the future. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s42768-023-00139-1.

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