Data on making uniform lignin building blocks via in-situ real-time monitoring of hydroxyethyl modification
In this work, a lab-designed apparatus was developed to collect and record the CO2 amount during the hydroxyethyl modification of lignin. We presented the CO2 volume amount and the production rate under different reaction conditions (80 – 120 °C and 2 – 6 hrs). Nuclear magnetic resonance spectroscop...
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Format: | Article |
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Elsevier
2020-12-01
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Series: | Data in Brief |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S2352340920313949 |
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author | Li-Yang Liu Kim Bessler Siwei Chen Mijung Cho Qi Hua Scott Renneckar |
author_facet | Li-Yang Liu Kim Bessler Siwei Chen Mijung Cho Qi Hua Scott Renneckar |
author_sort | Li-Yang Liu |
collection | DOAJ |
description | In this work, a lab-designed apparatus was developed to collect and record the CO2 amount during the hydroxyethyl modification of lignin. We presented the CO2 volume amount and the production rate under different reaction conditions (80 – 120 °C and 2 – 6 hrs). Nuclear magnetic resonance spectroscopy was performed to analyze the chemical structure of the hydroxyethyl lignin corresponding with different amounts of CO2 that evolved during the reaction. The aliphatic hydroxyl, aromatic hydroxyl, and carboxylic acid groups were analyzed and tabulated. The acetylated hydroxyethyl lignin samples were characterized by 13C NMR to obtain the aliphatic hydroxyl (primary and secondary), phenol (ortho substituted and ortho-free), hydroxyethyl, methoxy, and aromatic hydrogen groups semi-quantitatively. Fourier-transform infrared (FTIR) spectroscopy was adopted to analyze the surface functional groups including alkyl aryl ether bond, carboxylic acid groups, and aromatic hydroxyl groups. Gel permeation chromatography combined with a multi-angle light scattering detector and differential refractive index detector were used to obtain the molar mass of lignin before and after the modification. |
first_indexed | 2024-12-14T20:44:36Z |
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id | doaj.art-e7ea72694a1f4af7b68572bb7c419a5d |
institution | Directory Open Access Journal |
issn | 2352-3409 |
language | English |
last_indexed | 2024-12-14T20:44:36Z |
publishDate | 2020-12-01 |
publisher | Elsevier |
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series | Data in Brief |
spelling | doaj.art-e7ea72694a1f4af7b68572bb7c419a5d2022-12-21T22:48:07ZengElsevierData in Brief2352-34092020-12-0133106512Data on making uniform lignin building blocks via in-situ real-time monitoring of hydroxyethyl modificationLi-Yang Liu0Kim Bessler1Siwei Chen2Mijung Cho3Qi Hua4Scott Renneckar5Department of Wood Science, The University of British Columbia, 2424 Main Mall, Vancouver, British Columbia, CanadaDepartment of Wood Science, The University of British Columbia, 2424 Main Mall, Vancouver, British Columbia, CanadaDepartment of Wood Science, The University of British Columbia, 2424 Main Mall, Vancouver, British Columbia, CanadaDepartment of Wood Science, The University of British Columbia, 2424 Main Mall, Vancouver, British Columbia, CanadaDepartment of Wood Science, The University of British Columbia, 2424 Main Mall, Vancouver, British Columbia, CanadaCorresponding author.; Department of Wood Science, The University of British Columbia, 2424 Main Mall, Vancouver, British Columbia, CanadaIn this work, a lab-designed apparatus was developed to collect and record the CO2 amount during the hydroxyethyl modification of lignin. We presented the CO2 volume amount and the production rate under different reaction conditions (80 – 120 °C and 2 – 6 hrs). Nuclear magnetic resonance spectroscopy was performed to analyze the chemical structure of the hydroxyethyl lignin corresponding with different amounts of CO2 that evolved during the reaction. The aliphatic hydroxyl, aromatic hydroxyl, and carboxylic acid groups were analyzed and tabulated. The acetylated hydroxyethyl lignin samples were characterized by 13C NMR to obtain the aliphatic hydroxyl (primary and secondary), phenol (ortho substituted and ortho-free), hydroxyethyl, methoxy, and aromatic hydrogen groups semi-quantitatively. Fourier-transform infrared (FTIR) spectroscopy was adopted to analyze the surface functional groups including alkyl aryl ether bond, carboxylic acid groups, and aromatic hydroxyl groups. Gel permeation chromatography combined with a multi-angle light scattering detector and differential refractive index detector were used to obtain the molar mass of lignin before and after the modification.http://www.sciencedirect.com/science/article/pii/S2352340920313949ligninReal-time monitoringHydroxyethyl modificationCarbon storageBuilding blocksBioplastics |
spellingShingle | Li-Yang Liu Kim Bessler Siwei Chen Mijung Cho Qi Hua Scott Renneckar Data on making uniform lignin building blocks via in-situ real-time monitoring of hydroxyethyl modification Data in Brief lignin Real-time monitoring Hydroxyethyl modification Carbon storage Building blocks Bioplastics |
title | Data on making uniform lignin building blocks via in-situ real-time monitoring of hydroxyethyl modification |
title_full | Data on making uniform lignin building blocks via in-situ real-time monitoring of hydroxyethyl modification |
title_fullStr | Data on making uniform lignin building blocks via in-situ real-time monitoring of hydroxyethyl modification |
title_full_unstemmed | Data on making uniform lignin building blocks via in-situ real-time monitoring of hydroxyethyl modification |
title_short | Data on making uniform lignin building blocks via in-situ real-time monitoring of hydroxyethyl modification |
title_sort | data on making uniform lignin building blocks via in situ real time monitoring of hydroxyethyl modification |
topic | lignin Real-time monitoring Hydroxyethyl modification Carbon storage Building blocks Bioplastics |
url | http://www.sciencedirect.com/science/article/pii/S2352340920313949 |
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