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On-Site X-ray Fluorescence Spectrometry Measurement Strategy for Assessing the Sulfonation to Improve Chemimechanical Pulping Processes
[Image: see text] Minimizing the fiber property distribution would have the potential to improve the pulp properties and the process efficiency of chemimechanical pulp. To achieve this, it is essential to improve the level of knowledge of how evenly distributed the sulfonate concentration is between...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798522/ https://www.ncbi.nlm.nih.gov/pubmed/36591114 http://dx.doi.org/10.1021/acsomega.2c07086 |
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author | Rahman, Hafizur An, Siwen Norlin, Börje Persson, Erik Engstrand, Per Zeeshan, Faisal Granfeldt, Thomas Slavíček, Tomáš Pettersson, Gunilla |
author_facet | Rahman, Hafizur An, Siwen Norlin, Börje Persson, Erik Engstrand, Per Zeeshan, Faisal Granfeldt, Thomas Slavíček, Tomáš Pettersson, Gunilla |
author_sort | Rahman, Hafizur |
collection | PubMed |
description | [Image: see text] Minimizing the fiber property distribution would have the potential to improve the pulp properties and the process efficiency of chemimechanical pulp. To achieve this, it is essential to improve the level of knowledge of how evenly distributed the sulfonate concentration is between the individual chemimechanical pulp fibers. Due to the variation in quality between pulpwood and sawmill chips, as well as the on-chip screening method, it is difficult to develop an impregnation system that ensures the even distribution of sodium sulfite (Na(2)SO(3)) impregnation liquid. It is, therefore, crucial to measure the distribution of sulfonate groups within wood chips and fibers on a microscale. Typically, the degree of unevenness, i.e., the amount of fiber sulfonation and softening prior to defibration, is unknown on a microlevel due to excessively robust or complex processing methods. The degree of sulfonation at the fiber level can be determined by measuring the distribution of elemental sulfur and counterions of sulfonate groups, such as sodium or calcium. A miniaturized energy-dispersive X-ray fluorescence (ED-XRF) method has been developed to address this issue, enabling the analysis of sulfur distributions. It is effective enough to be applied to industrial laboratories for further development, i.e., improved image resolution and measurement time. |
format | Online Article Text |
id | pubmed-9798522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97985222022-12-30 On-Site X-ray Fluorescence Spectrometry Measurement Strategy for Assessing the Sulfonation to Improve Chemimechanical Pulping Processes Rahman, Hafizur An, Siwen Norlin, Börje Persson, Erik Engstrand, Per Zeeshan, Faisal Granfeldt, Thomas Slavíček, Tomáš Pettersson, Gunilla ACS Omega [Image: see text] Minimizing the fiber property distribution would have the potential to improve the pulp properties and the process efficiency of chemimechanical pulp. To achieve this, it is essential to improve the level of knowledge of how evenly distributed the sulfonate concentration is between the individual chemimechanical pulp fibers. Due to the variation in quality between pulpwood and sawmill chips, as well as the on-chip screening method, it is difficult to develop an impregnation system that ensures the even distribution of sodium sulfite (Na(2)SO(3)) impregnation liquid. It is, therefore, crucial to measure the distribution of sulfonate groups within wood chips and fibers on a microscale. Typically, the degree of unevenness, i.e., the amount of fiber sulfonation and softening prior to defibration, is unknown on a microlevel due to excessively robust or complex processing methods. The degree of sulfonation at the fiber level can be determined by measuring the distribution of elemental sulfur and counterions of sulfonate groups, such as sodium or calcium. A miniaturized energy-dispersive X-ray fluorescence (ED-XRF) method has been developed to address this issue, enabling the analysis of sulfur distributions. It is effective enough to be applied to industrial laboratories for further development, i.e., improved image resolution and measurement time. American Chemical Society 2022-12-15 /pmc/articles/PMC9798522/ /pubmed/36591114 http://dx.doi.org/10.1021/acsomega.2c07086 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/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 | Rahman, Hafizur An, Siwen Norlin, Börje Persson, Erik Engstrand, Per Zeeshan, Faisal Granfeldt, Thomas Slavíček, Tomáš Pettersson, Gunilla On-Site X-ray Fluorescence Spectrometry Measurement Strategy for Assessing the Sulfonation to Improve Chemimechanical Pulping Processes |
title | On-Site X-ray
Fluorescence Spectrometry Measurement
Strategy for Assessing the Sulfonation to Improve Chemimechanical
Pulping Processes |
title_full | On-Site X-ray
Fluorescence Spectrometry Measurement
Strategy for Assessing the Sulfonation to Improve Chemimechanical
Pulping Processes |
title_fullStr | On-Site X-ray
Fluorescence Spectrometry Measurement
Strategy for Assessing the Sulfonation to Improve Chemimechanical
Pulping Processes |
title_full_unstemmed | On-Site X-ray
Fluorescence Spectrometry Measurement
Strategy for Assessing the Sulfonation to Improve Chemimechanical
Pulping Processes |
title_short | On-Site X-ray
Fluorescence Spectrometry Measurement
Strategy for Assessing the Sulfonation to Improve Chemimechanical
Pulping Processes |
title_sort | on-site x-ray
fluorescence spectrometry measurement
strategy for assessing the sulfonation to improve chemimechanical
pulping processes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798522/ https://www.ncbi.nlm.nih.gov/pubmed/36591114 http://dx.doi.org/10.1021/acsomega.2c07086 |
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