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Thermostability of Organobentonite Modified with Poly(acrylic acid)
A new type of organobentonite foundry binder composed of a composite of bentonite (SN) and poly(acrylic acid) (PAA) was analyzed using thermal analysis (TG-DTG-DSC) and pyrolysis gas chromatography mass spectrometry (Py-GC/MS). The temperature range in which the composite retains its binding propert...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10221458/ https://www.ncbi.nlm.nih.gov/pubmed/37241253 http://dx.doi.org/10.3390/ma16103626 |
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author | Grabowska, Beata Cukrowicz, Sylwia Kaczmarska, Karolina Żymankowska-Kumon, Sylwia Bobrowski, Artur Tyliszczak, Bożena Mrówka, Natalia Maria |
author_facet | Grabowska, Beata Cukrowicz, Sylwia Kaczmarska, Karolina Żymankowska-Kumon, Sylwia Bobrowski, Artur Tyliszczak, Bożena Mrówka, Natalia Maria |
author_sort | Grabowska, Beata |
collection | PubMed |
description | A new type of organobentonite foundry binder composed of a composite of bentonite (SN) and poly(acrylic acid) (PAA) was analyzed using thermal analysis (TG-DTG-DSC) and pyrolysis gas chromatography mass spectrometry (Py-GC/MS). The temperature range in which the composite retains its binding properties was identified using thermal analysis of the composite and its components. Results showed that the thermal decomposition process is complex and involves physicochemical transformations that are mainly reversible at temperatures in the ranges of 20–100 °C (related to evaporation of solvent water) and 100–230 °C (related to intermolecular dehydration). The decomposition of PAA chains occurs between 230 and 300 °C, while complete decomposition of PAA and formation of organic decomposition products takes place at 300–500 °C. Dehydroxylation of montmorillonite (MMT) in bentonite begins at about 500 °C, which leads to a drastic structural transformation. An endothermic effect associated with the remodeling of the mineral structure was observed on the DSC curve in the range of 500–750 °C. The produced SN/PAA composite was found to be thermostable during degradation in both oxidative and inert atmosphere, similar to the starting bentonite, and even maintained over a relatively higher and wider temperature range compared to organic binding materials used. At the given temperatures of 300 °C and 800 °C, only CO(2) emissions occur from all the examined SN/PAA samples. There is no emission of compounds from the BTEX group. This means that the proposed binding material in the form of the MMT-PAA composite will not pose a threat to the environment and the workplace. |
format | Online Article Text |
id | pubmed-10221458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102214582023-05-28 Thermostability of Organobentonite Modified with Poly(acrylic acid) Grabowska, Beata Cukrowicz, Sylwia Kaczmarska, Karolina Żymankowska-Kumon, Sylwia Bobrowski, Artur Tyliszczak, Bożena Mrówka, Natalia Maria Materials (Basel) Article A new type of organobentonite foundry binder composed of a composite of bentonite (SN) and poly(acrylic acid) (PAA) was analyzed using thermal analysis (TG-DTG-DSC) and pyrolysis gas chromatography mass spectrometry (Py-GC/MS). The temperature range in which the composite retains its binding properties was identified using thermal analysis of the composite and its components. Results showed that the thermal decomposition process is complex and involves physicochemical transformations that are mainly reversible at temperatures in the ranges of 20–100 °C (related to evaporation of solvent water) and 100–230 °C (related to intermolecular dehydration). The decomposition of PAA chains occurs between 230 and 300 °C, while complete decomposition of PAA and formation of organic decomposition products takes place at 300–500 °C. Dehydroxylation of montmorillonite (MMT) in bentonite begins at about 500 °C, which leads to a drastic structural transformation. An endothermic effect associated with the remodeling of the mineral structure was observed on the DSC curve in the range of 500–750 °C. The produced SN/PAA composite was found to be thermostable during degradation in both oxidative and inert atmosphere, similar to the starting bentonite, and even maintained over a relatively higher and wider temperature range compared to organic binding materials used. At the given temperatures of 300 °C and 800 °C, only CO(2) emissions occur from all the examined SN/PAA samples. There is no emission of compounds from the BTEX group. This means that the proposed binding material in the form of the MMT-PAA composite will not pose a threat to the environment and the workplace. MDPI 2023-05-09 /pmc/articles/PMC10221458/ /pubmed/37241253 http://dx.doi.org/10.3390/ma16103626 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 Grabowska, Beata Cukrowicz, Sylwia Kaczmarska, Karolina Żymankowska-Kumon, Sylwia Bobrowski, Artur Tyliszczak, Bożena Mrówka, Natalia Maria Thermostability of Organobentonite Modified with Poly(acrylic acid) |
title | Thermostability of Organobentonite Modified with Poly(acrylic acid) |
title_full | Thermostability of Organobentonite Modified with Poly(acrylic acid) |
title_fullStr | Thermostability of Organobentonite Modified with Poly(acrylic acid) |
title_full_unstemmed | Thermostability of Organobentonite Modified with Poly(acrylic acid) |
title_short | Thermostability of Organobentonite Modified with Poly(acrylic acid) |
title_sort | thermostability of organobentonite modified with poly(acrylic acid) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10221458/ https://www.ncbi.nlm.nih.gov/pubmed/37241253 http://dx.doi.org/10.3390/ma16103626 |
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