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Valorizing Plastic-Contaminated Waste Streams through the Catalytic Hydrothermal Processing of Polypropylene with Lignocellulose
[Image: see text] Food waste is a promising resource for the production of fuels and chemicals. However, increasing plastic contamination has a large impact on the efficiency of conversion for the more established biological routes such as anaerobic digestion or fermentation. Here, we assessed a nov...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439709/ https://www.ncbi.nlm.nih.gov/pubmed/32832812 http://dx.doi.org/10.1021/acsomega.0c02854 |
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author | Hongthong, Sukanya Leese, Hannah S. Chuck, Christopher J. |
author_facet | Hongthong, Sukanya Leese, Hannah S. Chuck, Christopher J. |
author_sort | Hongthong, Sukanya |
collection | PubMed |
description | [Image: see text] Food waste is a promising resource for the production of fuels and chemicals. However, increasing plastic contamination has a large impact on the efficiency of conversion for the more established biological routes such as anaerobic digestion or fermentation. Here, we assessed a novel route through the hydrothermal liquefaction (HTL) of a model waste (pistachio hulls) and polypropylene (PP). Pure pistachio hulls gave a biocrude yield of 34% (w/w), though this reduced to 16% (w/w) on the addition of 50% PP in the mixture. The crude composition was a complex blend of phenolics, alkanes, carboxylic acids, and other oxygenates, which did not change substantially on the addition of PP. Pure PP does not breakdown at all under HTL conditions (350 °C, 15% solids loading), and even with biomass, there is only a small synergistic effect resulting in a conversion of 19% PP. This conversion was enhanced through using typical HTL catalysts including Fe, FeSO(4)·7H(2)O, MgSO(4)·H(2)O, ZnSO(4)·7H(2)O, ZSM-5, aluminosilicate, Y-zeolite, and Na(2)CO(3); the conversion of PP reached a maximum of 38% with the aluminosilicate, for example. However, the PP almost exclusively broke down into a solid-phase product, with no enhancement of the biocrude fraction. The mechanism was explored, and with the addition of the radical scavenger butylated hydroxytoluene (BHT), the conversion of plastic reduced substantially, demonstrating that radical formation is necessary. As a result, the plastic conversion was enhanced to over 50% through the addition of the co-solvent and hydrogen donor, formic acid, and the radical donor, hydrogen peroxide. The addition of formic acid also changed the crude composition, including more carboxylic acids and oxygenated species than the conversion of the biomass alone; however, the majority of the carbon distributed to the volatile organic gas fraction producing an array of short-chain volatile hydrocarbons, which potentially could be repolymerized as a polyolefin or combined with the biocrude for further processing. Catalytic HTL was therefore shown to be a promising method for the valorization of polyolefins with biomass under typical HTL conditions. |
format | Online Article Text |
id | pubmed-7439709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-74397092020-08-21 Valorizing Plastic-Contaminated Waste Streams through the Catalytic Hydrothermal Processing of Polypropylene with Lignocellulose Hongthong, Sukanya Leese, Hannah S. Chuck, Christopher J. ACS Omega [Image: see text] Food waste is a promising resource for the production of fuels and chemicals. However, increasing plastic contamination has a large impact on the efficiency of conversion for the more established biological routes such as anaerobic digestion or fermentation. Here, we assessed a novel route through the hydrothermal liquefaction (HTL) of a model waste (pistachio hulls) and polypropylene (PP). Pure pistachio hulls gave a biocrude yield of 34% (w/w), though this reduced to 16% (w/w) on the addition of 50% PP in the mixture. The crude composition was a complex blend of phenolics, alkanes, carboxylic acids, and other oxygenates, which did not change substantially on the addition of PP. Pure PP does not breakdown at all under HTL conditions (350 °C, 15% solids loading), and even with biomass, there is only a small synergistic effect resulting in a conversion of 19% PP. This conversion was enhanced through using typical HTL catalysts including Fe, FeSO(4)·7H(2)O, MgSO(4)·H(2)O, ZnSO(4)·7H(2)O, ZSM-5, aluminosilicate, Y-zeolite, and Na(2)CO(3); the conversion of PP reached a maximum of 38% with the aluminosilicate, for example. However, the PP almost exclusively broke down into a solid-phase product, with no enhancement of the biocrude fraction. The mechanism was explored, and with the addition of the radical scavenger butylated hydroxytoluene (BHT), the conversion of plastic reduced substantially, demonstrating that radical formation is necessary. As a result, the plastic conversion was enhanced to over 50% through the addition of the co-solvent and hydrogen donor, formic acid, and the radical donor, hydrogen peroxide. The addition of formic acid also changed the crude composition, including more carboxylic acids and oxygenated species than the conversion of the biomass alone; however, the majority of the carbon distributed to the volatile organic gas fraction producing an array of short-chain volatile hydrocarbons, which potentially could be repolymerized as a polyolefin or combined with the biocrude for further processing. Catalytic HTL was therefore shown to be a promising method for the valorization of polyolefins with biomass under typical HTL conditions. American Chemical Society 2020-08-07 /pmc/articles/PMC7439709/ /pubmed/32832812 http://dx.doi.org/10.1021/acsomega.0c02854 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Hongthong, Sukanya Leese, Hannah S. Chuck, Christopher J. Valorizing Plastic-Contaminated Waste Streams through the Catalytic Hydrothermal Processing of Polypropylene with Lignocellulose |
title | Valorizing Plastic-Contaminated Waste Streams through
the Catalytic Hydrothermal Processing of Polypropylene with Lignocellulose |
title_full | Valorizing Plastic-Contaminated Waste Streams through
the Catalytic Hydrothermal Processing of Polypropylene with Lignocellulose |
title_fullStr | Valorizing Plastic-Contaminated Waste Streams through
the Catalytic Hydrothermal Processing of Polypropylene with Lignocellulose |
title_full_unstemmed | Valorizing Plastic-Contaminated Waste Streams through
the Catalytic Hydrothermal Processing of Polypropylene with Lignocellulose |
title_short | Valorizing Plastic-Contaminated Waste Streams through
the Catalytic Hydrothermal Processing of Polypropylene with Lignocellulose |
title_sort | valorizing plastic-contaminated waste streams through
the catalytic hydrothermal processing of polypropylene with lignocellulose |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439709/ https://www.ncbi.nlm.nih.gov/pubmed/32832812 http://dx.doi.org/10.1021/acsomega.0c02854 |
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