Sulfonated Lignin-g-Styrene Polymer: Production and Characterization

Among sustainable alternatives for replacing fossil-based chemicals, lignin is widely available on earth, albeit the least utilized component of biomass. In this work, lignin was polymerized with styrene in aqueous emulsion systems. The reaction afforded a yield of 20 wt % under the conditions of 10...

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Main Authors: Nasim Ghavidel Darestani, Adrianna Tikka, Pedram Fatehi
Format: Article
Language:English
Published: MDPI AG 2018-08-01
Series:Polymers
Subjects:
NMR
Online Access:http://www.mdpi.com/2073-4360/10/8/928
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spelling doaj-c0b592198f8444cc987f831f720e9cf12020-11-24T23:29:23ZengMDPI AGPolymers2073-43602018-08-0110892810.3390/polym10080928polym10080928Sulfonated Lignin-g-Styrene Polymer: Production and CharacterizationNasim Ghavidel Darestani0Adrianna Tikka1Pedram Fatehi2Chemical Engineering and Chemistry Departments, Lakehead University, 955 Oliver Road, Thunder Bay, ON P7B 5E1, CanadaChemical Engineering and Chemistry Departments, Lakehead University, 955 Oliver Road, Thunder Bay, ON P7B 5E1, CanadaChemical Engineering and Chemistry Departments, Lakehead University, 955 Oliver Road, Thunder Bay, ON P7B 5E1, CanadaAmong sustainable alternatives for replacing fossil-based chemicals, lignin is widely available on earth, albeit the least utilized component of biomass. In this work, lignin was polymerized with styrene in aqueous emulsion systems. The reaction afforded a yield of 20 wt % under the conditions of 100 g/L lignin concentration, pH 2.5, 0.35 mol/L sodium dodecyl sulfate concentration, 5 mol/mol styrene/lignin ratio, 5 wt % initiator, 90 °C, and 2 h. The lignin-g-styrene product under the selected conditions had a grafting degree of 31 mol % of styrene, which was determined by quantitative proton nuclear magnetic resonance (NMR). The solvent addition to the reaction mixture and deoxygenation did not improve the yield of the polymerization reaction. The produced lignin-g-styrene polymer was then sulfonated using concentrated sulfuric acid. By introducing sulfonate group on the lignin-g-styrene polymers, the solubility and anionic charge density of 92 wt % (in a 10 g/L solution) and −2.4 meq/g, respectively, were obtained. Fourier-transform infrared (FTIR), static light scattering, two-dimensional COSY NMR, elemental analyses, and differential scanning calorimetry (DSC) were also employed to characterize the properties of the lignin-g-styrene and sulfonate lignin-g-styrene products. Overall, sulfonated lignin-g-styrene polymer with a high anionicity and water solubility was produced.http://www.mdpi.com/2073-4360/10/8/928polymerizationligninstyrenesulfonationsustainable polymerscharacterizationNMR
collection DOAJ
language English
format Article
sources DOAJ
author Nasim Ghavidel Darestani
Adrianna Tikka
Pedram Fatehi
spellingShingle Nasim Ghavidel Darestani
Adrianna Tikka
Pedram Fatehi
Sulfonated Lignin-g-Styrene Polymer: Production and Characterization
Polymers
polymerization
lignin
styrene
sulfonation
sustainable polymers
characterization
NMR
author_facet Nasim Ghavidel Darestani
Adrianna Tikka
Pedram Fatehi
author_sort Nasim Ghavidel Darestani
title Sulfonated Lignin-g-Styrene Polymer: Production and Characterization
title_short Sulfonated Lignin-g-Styrene Polymer: Production and Characterization
title_full Sulfonated Lignin-g-Styrene Polymer: Production and Characterization
title_fullStr Sulfonated Lignin-g-Styrene Polymer: Production and Characterization
title_full_unstemmed Sulfonated Lignin-g-Styrene Polymer: Production and Characterization
title_sort sulfonated lignin-g-styrene polymer: production and characterization
publisher MDPI AG
series Polymers
issn 2073-4360
publishDate 2018-08-01
description Among sustainable alternatives for replacing fossil-based chemicals, lignin is widely available on earth, albeit the least utilized component of biomass. In this work, lignin was polymerized with styrene in aqueous emulsion systems. The reaction afforded a yield of 20 wt % under the conditions of 100 g/L lignin concentration, pH 2.5, 0.35 mol/L sodium dodecyl sulfate concentration, 5 mol/mol styrene/lignin ratio, 5 wt % initiator, 90 °C, and 2 h. The lignin-g-styrene product under the selected conditions had a grafting degree of 31 mol % of styrene, which was determined by quantitative proton nuclear magnetic resonance (NMR). The solvent addition to the reaction mixture and deoxygenation did not improve the yield of the polymerization reaction. The produced lignin-g-styrene polymer was then sulfonated using concentrated sulfuric acid. By introducing sulfonate group on the lignin-g-styrene polymers, the solubility and anionic charge density of 92 wt % (in a 10 g/L solution) and −2.4 meq/g, respectively, were obtained. Fourier-transform infrared (FTIR), static light scattering, two-dimensional COSY NMR, elemental analyses, and differential scanning calorimetry (DSC) were also employed to characterize the properties of the lignin-g-styrene and sulfonate lignin-g-styrene products. Overall, sulfonated lignin-g-styrene polymer with a high anionicity and water solubility was produced.
topic polymerization
lignin
styrene
sulfonation
sustainable polymers
characterization
NMR
url http://www.mdpi.com/2073-4360/10/8/928
work_keys_str_mv AT nasimghavideldarestani sulfonatedligningstyrenepolymerproductionandcharacterization
AT adriannatikka sulfonatedligningstyrenepolymerproductionandcharacterization
AT pedramfatehi sulfonatedligningstyrenepolymerproductionandcharacterization
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