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Waste Plastic Polypropylene Activated Jujube Charcoal for Preparing High-Performance Phase Change Energy Storage Materials

The research on the high-value utilization of biomass has good application prospects and is conducive to sustainable development. In this paper, three different types of activators (potassium hydroxide, phosphoric acid, and polypropylene) were used to carbonize jujube branches at high temperatures o...

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Detalles Bibliográficos
Autores principales: Lv, Xifeng, Cao, Huan, Zhang, Rui, Shen, Xuehua, Wang, Xiaodong, Wang, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9919484/
https://www.ncbi.nlm.nih.gov/pubmed/36770513
http://dx.doi.org/10.3390/nano13030552
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author Lv, Xifeng
Cao, Huan
Zhang, Rui
Shen, Xuehua
Wang, Xiaodong
Wang, Fang
author_facet Lv, Xifeng
Cao, Huan
Zhang, Rui
Shen, Xuehua
Wang, Xiaodong
Wang, Fang
author_sort Lv, Xifeng
collection PubMed
description The research on the high-value utilization of biomass has good application prospects and is conducive to sustainable development. In this paper, three different types of activators (potassium hydroxide, phosphoric acid, and polypropylene) were used to carbonize jujube branches at high temperatures of 600 °C and 800 °C, and then the PEG/jujube charcoal composite phase change materials (PCM) were prepared by vacuum impregnation of polyethylene glycol (PEG). The results showed that the carbon support activated by polypropylene (PP) had a richer pore size distribution than the other two activation methods, and the 800 °C carbonization carrier loaded PEG had a higher phase change enthalpy than the composite material at 600 °C. The mesoporous and macroporous structures were staggered with PP-activated jujube charcoal at 800 °C, with a specific surface area of 1082.2 m²/g, the melting enthalpy of the composite material reached 114.92 J/g, and the enthalpy of solidification reached 106.15 J/g after PEG loading. The diffraction peak of the composite phase change material was the superposition of PEG and carbon matrix, which proved that the loading process was physical adsorption. After 200 thermal cycles, the melting enthalpy and crystallization enthalpy were only reduced by 4.3% and 4.1%, respectively, and they remained stable and leak-free at the melting point of PEG for 2 h, demonstrating good thermal stability of the composite phase change materials. In summary, PP has obvious advantages over traditional activation, and the carbon-supported PEG phase change composite after PP activation is a biochar energy storage material with excellent performance.
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spelling pubmed-99194842023-02-12 Waste Plastic Polypropylene Activated Jujube Charcoal for Preparing High-Performance Phase Change Energy Storage Materials Lv, Xifeng Cao, Huan Zhang, Rui Shen, Xuehua Wang, Xiaodong Wang, Fang Nanomaterials (Basel) Article The research on the high-value utilization of biomass has good application prospects and is conducive to sustainable development. In this paper, three different types of activators (potassium hydroxide, phosphoric acid, and polypropylene) were used to carbonize jujube branches at high temperatures of 600 °C and 800 °C, and then the PEG/jujube charcoal composite phase change materials (PCM) were prepared by vacuum impregnation of polyethylene glycol (PEG). The results showed that the carbon support activated by polypropylene (PP) had a richer pore size distribution than the other two activation methods, and the 800 °C carbonization carrier loaded PEG had a higher phase change enthalpy than the composite material at 600 °C. The mesoporous and macroporous structures were staggered with PP-activated jujube charcoal at 800 °C, with a specific surface area of 1082.2 m²/g, the melting enthalpy of the composite material reached 114.92 J/g, and the enthalpy of solidification reached 106.15 J/g after PEG loading. The diffraction peak of the composite phase change material was the superposition of PEG and carbon matrix, which proved that the loading process was physical adsorption. After 200 thermal cycles, the melting enthalpy and crystallization enthalpy were only reduced by 4.3% and 4.1%, respectively, and they remained stable and leak-free at the melting point of PEG for 2 h, demonstrating good thermal stability of the composite phase change materials. In summary, PP has obvious advantages over traditional activation, and the carbon-supported PEG phase change composite after PP activation is a biochar energy storage material with excellent performance. MDPI 2023-01-29 /pmc/articles/PMC9919484/ /pubmed/36770513 http://dx.doi.org/10.3390/nano13030552 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lv, Xifeng
Cao, Huan
Zhang, Rui
Shen, Xuehua
Wang, Xiaodong
Wang, Fang
Waste Plastic Polypropylene Activated Jujube Charcoal for Preparing High-Performance Phase Change Energy Storage Materials
title Waste Plastic Polypropylene Activated Jujube Charcoal for Preparing High-Performance Phase Change Energy Storage Materials
title_full Waste Plastic Polypropylene Activated Jujube Charcoal for Preparing High-Performance Phase Change Energy Storage Materials
title_fullStr Waste Plastic Polypropylene Activated Jujube Charcoal for Preparing High-Performance Phase Change Energy Storage Materials
title_full_unstemmed Waste Plastic Polypropylene Activated Jujube Charcoal for Preparing High-Performance Phase Change Energy Storage Materials
title_short Waste Plastic Polypropylene Activated Jujube Charcoal for Preparing High-Performance Phase Change Energy Storage Materials
title_sort waste plastic polypropylene activated jujube charcoal for preparing high-performance phase change energy storage materials
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9919484/
https://www.ncbi.nlm.nih.gov/pubmed/36770513
http://dx.doi.org/10.3390/nano13030552
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