Effect of Chemical Structure on Pyrolysis Behavior of Alcell Mild Acidolysis Lignin

In this study, two purified mild acidolysis lignins (MAL) extracted from triploid poplar, i.e., Alcell MAL and Alkali MAL, were compared. Some properties, including elemental contents, higher heating value (HHV), functional hydroxyl group compositions, and molecular weights, were tested to character...

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Main Authors: Chao Liu, Jia-Jin Liang, Shu-Bin Wu, Yu-Bin Deng
Format: Article
Language:English
Published: North Carolina State University 2014-12-01
Series:BioResources
Subjects:
Online Access:http://ojs.cnr.ncsu.edu/index.php/BioRes/article/view/BioRes_10_1_1073_Liu_Pyrolysis_Behavior_Alcell_Lignin
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author Chao Liu
Jia-Jin Liang
Shu-Bin Wu
Yu-Bin Deng
author_facet Chao Liu
Jia-Jin Liang
Shu-Bin Wu
Yu-Bin Deng
author_sort Chao Liu
collection DOAJ
description In this study, two purified mild acidolysis lignins (MAL) extracted from triploid poplar, i.e., Alcell MAL and Alkali MAL, were compared. Some properties, including elemental contents, higher heating value (HHV), functional hydroxyl group compositions, and molecular weights, were tested to characterize the structure of these two MALs. The releasing laws of gases and the distribution of products were also investigated through the use of thermogravimetric Fourier transform infrared (TG-FTIR) and pyrolysis-gas chromatography combined with mass spectrometry (Py-GC/MS). The results showed that both MALs had pyrolytic advantages, largely because of their unique chemical structures. However, although the species of volatiles from Alkali MAL were similar to those from Alcell MAL, the releasing temperature range for Alcell MAL was relatively narrow and the volatiles from it were concentrated. Among the fast pyrolytic products, phenols were the most abundant. The yield of 2,6-dimethoxy-4-(2-propenyl)phenol, which was the dominant product, was 25.66% for Alcell MAL and 20.77% for Alkali MAL, respectively. Overall, pyrolytic products from Alcell MAL were more enriched.
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spelling doaj.art-956bf7ee538448a78b3cfb39640af0932022-12-22T02:48:47ZengNorth Carolina State UniversityBioResources1930-21261930-21262014-12-011011073108410.15376/biores.10.1.1073-1084Effect of Chemical Structure on Pyrolysis Behavior of Alcell Mild Acidolysis LigninChao Liu0Jia-Jin Liang1Shu-Bin Wu2Yu-Bin Deng3State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, Guangdong 510640, PR China; ChinaState Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, Guangdong 510640, PR China; ChinaState Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, Guangdong 510640, PR China; ChinaState Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, Guangdong 510640, PR China; ChinaIn this study, two purified mild acidolysis lignins (MAL) extracted from triploid poplar, i.e., Alcell MAL and Alkali MAL, were compared. Some properties, including elemental contents, higher heating value (HHV), functional hydroxyl group compositions, and molecular weights, were tested to characterize the structure of these two MALs. The releasing laws of gases and the distribution of products were also investigated through the use of thermogravimetric Fourier transform infrared (TG-FTIR) and pyrolysis-gas chromatography combined with mass spectrometry (Py-GC/MS). The results showed that both MALs had pyrolytic advantages, largely because of their unique chemical structures. However, although the species of volatiles from Alkali MAL were similar to those from Alcell MAL, the releasing temperature range for Alcell MAL was relatively narrow and the volatiles from it were concentrated. Among the fast pyrolytic products, phenols were the most abundant. The yield of 2,6-dimethoxy-4-(2-propenyl)phenol, which was the dominant product, was 25.66% for Alcell MAL and 20.77% for Alkali MAL, respectively. Overall, pyrolytic products from Alcell MAL were more enriched.http://ojs.cnr.ncsu.edu/index.php/BioRes/article/view/BioRes_10_1_1073_Liu_Pyrolysis_Behavior_Alcell_LigninAlcell MALQuantitative 31P-NMRTG-FTIRPy-GC/MS
spellingShingle Chao Liu
Jia-Jin Liang
Shu-Bin Wu
Yu-Bin Deng
Effect of Chemical Structure on Pyrolysis Behavior of Alcell Mild Acidolysis Lignin
BioResources
Alcell MAL
Quantitative 31P-NMR
TG-FTIR
Py-GC/MS
title Effect of Chemical Structure on Pyrolysis Behavior of Alcell Mild Acidolysis Lignin
title_full Effect of Chemical Structure on Pyrolysis Behavior of Alcell Mild Acidolysis Lignin
title_fullStr Effect of Chemical Structure on Pyrolysis Behavior of Alcell Mild Acidolysis Lignin
title_full_unstemmed Effect of Chemical Structure on Pyrolysis Behavior of Alcell Mild Acidolysis Lignin
title_short Effect of Chemical Structure on Pyrolysis Behavior of Alcell Mild Acidolysis Lignin
title_sort effect of chemical structure on pyrolysis behavior of alcell mild acidolysis lignin
topic Alcell MAL
Quantitative 31P-NMR
TG-FTIR
Py-GC/MS
url http://ojs.cnr.ncsu.edu/index.php/BioRes/article/view/BioRes_10_1_1073_Liu_Pyrolysis_Behavior_Alcell_Lignin
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