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Lignin‐g‐poly(acrylamide)‐g‐poly(diallyldimethyl‐ ammonium chloride): Synthesis, Characterization and Applications
The search for a renewable substitute to petroleum‐based products has fueled increasing research on lignin, an under‐utilized product from pulping processes. In this work, lignin was copolymerized with acrylamide (AM) and diallyldimethylammonium chloride (DADMAC) under acidic conditions with Na(2)S(...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110050/ https://www.ncbi.nlm.nih.gov/pubmed/30155399 http://dx.doi.org/10.1002/open.201800105 |
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author | Price, Jacquelyn Tara Gao, Weijue Fatehi, Pedram |
author_facet | Price, Jacquelyn Tara Gao, Weijue Fatehi, Pedram |
author_sort | Price, Jacquelyn Tara |
collection | PubMed |
description | The search for a renewable substitute to petroleum‐based products has fueled increasing research on lignin, an under‐utilized product from pulping processes. In this work, lignin was copolymerized with acrylamide (AM) and diallyldimethylammonium chloride (DADMAC) under acidic conditions with Na(2)S(2)O(8) as an initiator, generating a cationic water‐soluble lignin‐g‐P(AM)‐g‐P(DADMAC) copolymer. The optimal reaction conditions, using a 5×4 factorial design experiment, were determined to be an AM/DADMAC/lignin molar ratio of 5.5:2.4:1, 90 °C, 0.26 mol L(−1) of lignin, and pH 2. Under the optimal reaction conditions, the resulting lignin‐g‐P(AM)‐g‐P(DADMAC) copolymer was 83 % soluble in an aqueous solution (at 10 g L(−1)) and at neutral pH. The copolymer had a charge density of 1.27 meq g(−1), molecular weight of (1.33±0.08) ×10(6), an AM grafting ratio of 112 wt %, and a DADMAC grafting ratio of 20 wt %. In addition, the activation energy for producing this copolymer as well as the thermal and rheological properties of the copolymer were determined. The flocculation performance of lignin‐g‐P(AM)‐g‐P(DADMAC) copolymer was evaluated in a kaolin suspension, which showed that the lignin copolymer had a comparable flocculation efficiency with the synthetic analogue of P(AM)‐g‐P(DADMAC) at pH 6. |
format | Online Article Text |
id | pubmed-6110050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61100502018-08-28 Lignin‐g‐poly(acrylamide)‐g‐poly(diallyldimethyl‐ ammonium chloride): Synthesis, Characterization and Applications Price, Jacquelyn Tara Gao, Weijue Fatehi, Pedram ChemistryOpen Full Papers The search for a renewable substitute to petroleum‐based products has fueled increasing research on lignin, an under‐utilized product from pulping processes. In this work, lignin was copolymerized with acrylamide (AM) and diallyldimethylammonium chloride (DADMAC) under acidic conditions with Na(2)S(2)O(8) as an initiator, generating a cationic water‐soluble lignin‐g‐P(AM)‐g‐P(DADMAC) copolymer. The optimal reaction conditions, using a 5×4 factorial design experiment, were determined to be an AM/DADMAC/lignin molar ratio of 5.5:2.4:1, 90 °C, 0.26 mol L(−1) of lignin, and pH 2. Under the optimal reaction conditions, the resulting lignin‐g‐P(AM)‐g‐P(DADMAC) copolymer was 83 % soluble in an aqueous solution (at 10 g L(−1)) and at neutral pH. The copolymer had a charge density of 1.27 meq g(−1), molecular weight of (1.33±0.08) ×10(6), an AM grafting ratio of 112 wt %, and a DADMAC grafting ratio of 20 wt %. In addition, the activation energy for producing this copolymer as well as the thermal and rheological properties of the copolymer were determined. The flocculation performance of lignin‐g‐P(AM)‐g‐P(DADMAC) copolymer was evaluated in a kaolin suspension, which showed that the lignin copolymer had a comparable flocculation efficiency with the synthetic analogue of P(AM)‐g‐P(DADMAC) at pH 6. John Wiley and Sons Inc. 2018-08-27 /pmc/articles/PMC6110050/ /pubmed/30155399 http://dx.doi.org/10.1002/open.201800105 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Full Papers Price, Jacquelyn Tara Gao, Weijue Fatehi, Pedram Lignin‐g‐poly(acrylamide)‐g‐poly(diallyldimethyl‐ ammonium chloride): Synthesis, Characterization and Applications |
title | Lignin‐g‐poly(acrylamide)‐g‐poly(diallyldimethyl‐ ammonium chloride): Synthesis, Characterization and Applications |
title_full | Lignin‐g‐poly(acrylamide)‐g‐poly(diallyldimethyl‐ ammonium chloride): Synthesis, Characterization and Applications |
title_fullStr | Lignin‐g‐poly(acrylamide)‐g‐poly(diallyldimethyl‐ ammonium chloride): Synthesis, Characterization and Applications |
title_full_unstemmed | Lignin‐g‐poly(acrylamide)‐g‐poly(diallyldimethyl‐ ammonium chloride): Synthesis, Characterization and Applications |
title_short | Lignin‐g‐poly(acrylamide)‐g‐poly(diallyldimethyl‐ ammonium chloride): Synthesis, Characterization and Applications |
title_sort | lignin‐g‐poly(acrylamide)‐g‐poly(diallyldimethyl‐ ammonium chloride): synthesis, characterization and applications |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110050/ https://www.ncbi.nlm.nih.gov/pubmed/30155399 http://dx.doi.org/10.1002/open.201800105 |
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