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Sulfuric Acid-Catalyzed Dehydratization of Carbohydrates for the Production of Adhesive Precursors
[Image: see text] Carbohydrates and hexose-derived 5-hydroxymethylfurfural (5-HMF) are platform chemicals for the synthesis of sustainable binders. New, greener approaches aim at the development of production systems, which minimize process steps and avoid organic solvents or other auxiliaries that...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246703/ https://www.ncbi.nlm.nih.gov/pubmed/34235336 http://dx.doi.org/10.1021/acsomega.1c02075 |
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author | Sailer-Kronlachner, Wilfried Thoma, Catherine Böhmdorfer, Stefan Bacher, Markus Konnerth, Johannes Rosenau, Thomas Potthast, Antje Solt, Pia van Herwijnen, Hendrikus W. G. |
author_facet | Sailer-Kronlachner, Wilfried Thoma, Catherine Böhmdorfer, Stefan Bacher, Markus Konnerth, Johannes Rosenau, Thomas Potthast, Antje Solt, Pia van Herwijnen, Hendrikus W. G. |
author_sort | Sailer-Kronlachner, Wilfried |
collection | PubMed |
description | [Image: see text] Carbohydrates and hexose-derived 5-hydroxymethylfurfural (5-HMF) are platform chemicals for the synthesis of sustainable binders. New, greener approaches aim at the development of production systems, which minimize process steps and avoid organic solvents or other auxiliaries that could interfere with subsequent resin synthesis. In our work, carbohydrate solutions rich in 5-hydroxymethylfurfural (5-HMF) were produced using a continuous-flow microreactor and diluted H(2)SO(4) as the catalyst. After optimization of the process conditions (temperature, reaction time, catalyst content), a 5-HMF yield of 49% was obtained at a low reaction time of 0.6 min and a catalyst concentration of 1% at 175 °C and 17 bar pressure. Extensive rehydration of the product was avoided by efficient immediate cooling of the reaction solution. The stability of the reaction system was improved by increasing the inner diameter of the capillary in the flow reactor to 2 mm. Advantageously, the obtained reaction mixtures are used directly as precursors in the development of sustainable binder systems, without the need of additional purification, filtration, or extraction steps. |
format | Online Article Text |
id | pubmed-8246703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82467032021-07-06 Sulfuric Acid-Catalyzed Dehydratization of Carbohydrates for the Production of Adhesive Precursors Sailer-Kronlachner, Wilfried Thoma, Catherine Böhmdorfer, Stefan Bacher, Markus Konnerth, Johannes Rosenau, Thomas Potthast, Antje Solt, Pia van Herwijnen, Hendrikus W. G. ACS Omega [Image: see text] Carbohydrates and hexose-derived 5-hydroxymethylfurfural (5-HMF) are platform chemicals for the synthesis of sustainable binders. New, greener approaches aim at the development of production systems, which minimize process steps and avoid organic solvents or other auxiliaries that could interfere with subsequent resin synthesis. In our work, carbohydrate solutions rich in 5-hydroxymethylfurfural (5-HMF) were produced using a continuous-flow microreactor and diluted H(2)SO(4) as the catalyst. After optimization of the process conditions (temperature, reaction time, catalyst content), a 5-HMF yield of 49% was obtained at a low reaction time of 0.6 min and a catalyst concentration of 1% at 175 °C and 17 bar pressure. Extensive rehydration of the product was avoided by efficient immediate cooling of the reaction solution. The stability of the reaction system was improved by increasing the inner diameter of the capillary in the flow reactor to 2 mm. Advantageously, the obtained reaction mixtures are used directly as precursors in the development of sustainable binder systems, without the need of additional purification, filtration, or extraction steps. American Chemical Society 2021-06-15 /pmc/articles/PMC8246703/ /pubmed/34235336 http://dx.doi.org/10.1021/acsomega.1c02075 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Sailer-Kronlachner, Wilfried Thoma, Catherine Böhmdorfer, Stefan Bacher, Markus Konnerth, Johannes Rosenau, Thomas Potthast, Antje Solt, Pia van Herwijnen, Hendrikus W. G. Sulfuric Acid-Catalyzed Dehydratization of Carbohydrates for the Production of Adhesive Precursors |
title | Sulfuric Acid-Catalyzed Dehydratization of Carbohydrates
for the Production of Adhesive Precursors |
title_full | Sulfuric Acid-Catalyzed Dehydratization of Carbohydrates
for the Production of Adhesive Precursors |
title_fullStr | Sulfuric Acid-Catalyzed Dehydratization of Carbohydrates
for the Production of Adhesive Precursors |
title_full_unstemmed | Sulfuric Acid-Catalyzed Dehydratization of Carbohydrates
for the Production of Adhesive Precursors |
title_short | Sulfuric Acid-Catalyzed Dehydratization of Carbohydrates
for the Production of Adhesive Precursors |
title_sort | sulfuric acid-catalyzed dehydratization of carbohydrates
for the production of adhesive precursors |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246703/ https://www.ncbi.nlm.nih.gov/pubmed/34235336 http://dx.doi.org/10.1021/acsomega.1c02075 |
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