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Base- or acid-assisted polystyrene plastic degradation in supercritical CO(2)

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(2) (Sc-...

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Autores principales: Liu, Yanbing, Shi, Jinwen, Mao, Liuhao, Lu, Bingru, Kang, Xing, Jin, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10023313/
https://www.ncbi.nlm.nih.gov/pubmed/37359813
http://dx.doi.org/10.1007/s42768-023-00139-1
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author Liu, Yanbing
Shi, Jinwen
Mao, Liuhao
Lu, Bingru
Kang, Xing
Jin, Hui
author_facet Liu, Yanbing
Shi, Jinwen
Mao, Liuhao
Lu, Bingru
Kang, Xing
Jin, Hui
author_sort Liu, Yanbing
collection PubMed
description 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(2) (Sc-CO(2)) 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(2), and consumed 81.2/71.5±5 mL of CO(2). Sc-CO(2) created a homogeneous environment, which made PS highly dispersed and uniformly heated, thus promoting the degradation of PS. Moreover, Sc-CO(2) also reacted with the degradation products to produce new CO and more CH(4) and C(2)H(x) (x=4, 6). Adding NaOH/HCl solution not only improved the solubility of PS in Sc-CO(2), 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(2) 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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spelling pubmed-100233132023-03-21 Base- or acid-assisted polystyrene plastic degradation in supercritical CO(2) Liu, Yanbing Shi, Jinwen Mao, Liuhao Lu, Bingru Kang, Xing Jin, Hui Waste Dispos Sustain Energy Article 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(2) (Sc-CO(2)) 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(2), and consumed 81.2/71.5±5 mL of CO(2). Sc-CO(2) created a homogeneous environment, which made PS highly dispersed and uniformly heated, thus promoting the degradation of PS. Moreover, Sc-CO(2) also reacted with the degradation products to produce new CO and more CH(4) and C(2)H(x) (x=4, 6). Adding NaOH/HCl solution not only improved the solubility of PS in Sc-CO(2), 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(2) 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. Springer Nature Singapore 2023-03-18 /pmc/articles/PMC10023313/ /pubmed/37359813 http://dx.doi.org/10.1007/s42768-023-00139-1 Text en © Zhejiang University Press 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Liu, Yanbing
Shi, Jinwen
Mao, Liuhao
Lu, Bingru
Kang, Xing
Jin, Hui
Base- or acid-assisted polystyrene plastic degradation in supercritical CO(2)
title Base- or acid-assisted polystyrene plastic degradation in supercritical CO(2)
title_full Base- or acid-assisted polystyrene plastic degradation in supercritical CO(2)
title_fullStr Base- or acid-assisted polystyrene plastic degradation in supercritical CO(2)
title_full_unstemmed Base- or acid-assisted polystyrene plastic degradation in supercritical CO(2)
title_short Base- or acid-assisted polystyrene plastic degradation in supercritical CO(2)
title_sort base- or acid-assisted polystyrene plastic degradation in supercritical co(2)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10023313/
https://www.ncbi.nlm.nih.gov/pubmed/37359813
http://dx.doi.org/10.1007/s42768-023-00139-1
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