Qualitative Structural Characterization of Two Lignin Samples and Quantitative Determination of Hydroxyl and Methoxyl Functional Groups in Kraft Lignin via Acetylation

In this research, two types of lignin, i.e. one extracted from industrial waste water of the Iran wood and paper (choka) factory as black liquor and another provided from Aldrich company, were studied. Firstly, the lignin was precipitated from its black liquor by a dilute acid and was then purified...

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Autores principales: Mehdi Abdolahi, Said amir Mosavian, Akbar Varamsh, Amin Asadi
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Publicado: Regional Information Center for Science and Technology (RICeST) 2017
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spelling oai:doaj.org-article:f8664760db0546e6a0857b11b3b297c72021-12-02T11:55:26ZQualitative Structural Characterization of Two Lignin Samples and Quantitative Determination of Hydroxyl and Methoxyl Functional Groups in Kraft Lignin via Acetylation1735-09132383-112X10.22092/ijwpr.2017.109402.1388https://doaj.org/article/f8664760db0546e6a0857b11b3b297c72017-10-01T00:00:00Zhttp://ijwpr.areeo.ac.ir/article_113508_944380991fe46b4445912a34eef84641.pdfhttps://doaj.org/toc/1735-0913https://doaj.org/toc/2383-112XIn this research, two types of lignin, i.e. one extracted from industrial waste water of the Iran wood and paper (choka) factory as black liquor and another provided from Aldrich company, were studied. Firstly, the lignin was precipitated from its black liquor by a dilute acid and was then purified by dissolving in tetrahydrofuran (THF). Lignin samples were characterized using Fourier transform infrared (FTIR) and proton nuclear magnetic resonance (1HNMR) spectroscopies. It was found from results that the Aldrich lignin has a structure similar with the lignosulfonate while lignin extracted from black liquor does not have a hydrophilic sulfonate group and has a Kraft lignin structure. Using acetylation of Kraft lignin and complementary characterization with 1HNMR spectroscopy, the ratio of hydroxyl functional groups to methoxy groups was calculated to be 1.11 to 1, and amount of the hydroxyl groups was calculated to be 5.91 mmol/g of acetylated lignin, where 53% of the hydroxyl groups is related to the aromatic hydroxyl groups. By having the molecular weight of the Kraft lignin which was obtained from the gel permeation chromatography (GPC) analysis of the acetylated Kraft lignin to be 1260 g/mol, average number of the hydroxyl groups per acetylated lignin chain was calculated to be 7.44.Mehdi AbdolahiSaid amir MosavianAkbar VaramshAmin AsadiRegional Information Center for Science and Technology (RICeST)articleLIGNINAcetylationStructural characterizationFTIR1H-NMRForestrySD1-669.5FAتحقیقات علوم چوب و کاغذ ایران, Vol 32, Iss 3, Pp 369-381 (2017)
institution DOAJ
collection DOAJ
language FA
topic LIGNIN
Acetylation
Structural characterization
FTIR
1H-NMR
Forestry
SD1-669.5
spellingShingle LIGNIN
Acetylation
Structural characterization
FTIR
1H-NMR
Forestry
SD1-669.5
Mehdi Abdolahi
Said amir Mosavian
Akbar Varamsh
Amin Asadi
Qualitative Structural Characterization of Two Lignin Samples and Quantitative Determination of Hydroxyl and Methoxyl Functional Groups in Kraft Lignin via Acetylation
description In this research, two types of lignin, i.e. one extracted from industrial waste water of the Iran wood and paper (choka) factory as black liquor and another provided from Aldrich company, were studied. Firstly, the lignin was precipitated from its black liquor by a dilute acid and was then purified by dissolving in tetrahydrofuran (THF). Lignin samples were characterized using Fourier transform infrared (FTIR) and proton nuclear magnetic resonance (1HNMR) spectroscopies. It was found from results that the Aldrich lignin has a structure similar with the lignosulfonate while lignin extracted from black liquor does not have a hydrophilic sulfonate group and has a Kraft lignin structure. Using acetylation of Kraft lignin and complementary characterization with 1HNMR spectroscopy, the ratio of hydroxyl functional groups to methoxy groups was calculated to be 1.11 to 1, and amount of the hydroxyl groups was calculated to be 5.91 mmol/g of acetylated lignin, where 53% of the hydroxyl groups is related to the aromatic hydroxyl groups. By having the molecular weight of the Kraft lignin which was obtained from the gel permeation chromatography (GPC) analysis of the acetylated Kraft lignin to be 1260 g/mol, average number of the hydroxyl groups per acetylated lignin chain was calculated to be 7.44.
format article
author Mehdi Abdolahi
Said amir Mosavian
Akbar Varamsh
Amin Asadi
author_facet Mehdi Abdolahi
Said amir Mosavian
Akbar Varamsh
Amin Asadi
author_sort Mehdi Abdolahi
title Qualitative Structural Characterization of Two Lignin Samples and Quantitative Determination of Hydroxyl and Methoxyl Functional Groups in Kraft Lignin via Acetylation
title_short Qualitative Structural Characterization of Two Lignin Samples and Quantitative Determination of Hydroxyl and Methoxyl Functional Groups in Kraft Lignin via Acetylation
title_full Qualitative Structural Characterization of Two Lignin Samples and Quantitative Determination of Hydroxyl and Methoxyl Functional Groups in Kraft Lignin via Acetylation
title_fullStr Qualitative Structural Characterization of Two Lignin Samples and Quantitative Determination of Hydroxyl and Methoxyl Functional Groups in Kraft Lignin via Acetylation
title_full_unstemmed Qualitative Structural Characterization of Two Lignin Samples and Quantitative Determination of Hydroxyl and Methoxyl Functional Groups in Kraft Lignin via Acetylation
title_sort qualitative structural characterization of two lignin samples and quantitative determination of hydroxyl and methoxyl functional groups in kraft lignin via acetylation
publisher Regional Information Center for Science and Technology (RICeST)
publishDate 2017
url https://doaj.org/article/f8664760db0546e6a0857b11b3b297c7
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AT saidamirmosavian qualitativestructuralcharacterizationoftwoligninsamplesandquantitativedeterminationofhydroxylandmethoxylfunctionalgroupsinkraftligninviaacetylation
AT akbarvaramsh qualitativestructuralcharacterizationoftwoligninsamplesandquantitativedeterminationofhydroxylandmethoxylfunctionalgroupsinkraftligninviaacetylation
AT aminasadi qualitativestructuralcharacterizationoftwoligninsamplesandquantitativedeterminationofhydroxylandmethoxylfunctionalgroupsinkraftligninviaacetylation
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