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Preparation of PLA blends by polycondensation of D,L-lactic acid using supported 12-tungstophosphoric acid as a heterogeneous catalyst
Poly(lactic acid) (PLA) is a significant polymer that is based on renewable biomass resources. The production of PLA by polycondensation using heterogeneous catalysis is a focus for sustainable and economical processes. A series of samples comprising 12-tungstophosphoric acid (H(3)PW) supported on a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539807/ https://www.ncbi.nlm.nih.gov/pubmed/31193779 http://dx.doi.org/10.1016/j.heliyon.2019.e01810 |
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author | Chafran, Liana S. Paiva, Mateus F. França, Juliene O.C. Sales, Maria José A. Dias, Sílvia C.L. Dias, José A. |
author_facet | Chafran, Liana S. Paiva, Mateus F. França, Juliene O.C. Sales, Maria José A. Dias, Sílvia C.L. Dias, José A. |
author_sort | Chafran, Liana S. |
collection | PubMed |
description | Poly(lactic acid) (PLA) is a significant polymer that is based on renewable biomass resources. The production of PLA by polycondensation using heterogeneous catalysis is a focus for sustainable and economical processes. A series of samples comprising 12-tungstophosphoric acid (H(3)PW) supported on activated carbon, silica, and alumina induced the catalytic polymerization of D,L-lactic acid to form blends of PLA. The catalysts were characterized by multiple techniques to confirm the integrity of the Keggin anion as well as the acidity, which is the key property for relating structure to activity. The best reaction conditions were established for H(3)PW/C and tested for the other supported catalysts. The obtained polymer was a blend that was characterized as an enantiomeric excess (ee) of as much as 95% L-PLA (PLLA) with a mass average molar mass (M(w)) of approximately 14,900 daltons. The role of H(3)PW in these polymerizations was demonstrated, i.e., without the Keggin acid, only oligomeric units (M(w) < 10,000 daltons) could be obtained. Additionally, inverse relationships between the M(w) of PLA and the enthalpy (–ΔH) of the strongest sites of the catalysts were distinguished, i.e., PLA(Mw-H3PW/C) > PLA(Mw-H3PW/Al2O3) > PLA(Mw-H3PW/SiO2), whereas the acidity (–ΔH) order was as follows: H(3)PW/SiO(2) > H(3)PW/Al(2)O(3) > H(3)PW/C. These findings could be attributed to the correct tuning of strength and the accessibility of the sites to produce longer polymeric chains. |
format | Online Article Text |
id | pubmed-6539807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-65398072019-06-03 Preparation of PLA blends by polycondensation of D,L-lactic acid using supported 12-tungstophosphoric acid as a heterogeneous catalyst Chafran, Liana S. Paiva, Mateus F. França, Juliene O.C. Sales, Maria José A. Dias, Sílvia C.L. Dias, José A. Heliyon Article Poly(lactic acid) (PLA) is a significant polymer that is based on renewable biomass resources. The production of PLA by polycondensation using heterogeneous catalysis is a focus for sustainable and economical processes. A series of samples comprising 12-tungstophosphoric acid (H(3)PW) supported on activated carbon, silica, and alumina induced the catalytic polymerization of D,L-lactic acid to form blends of PLA. The catalysts were characterized by multiple techniques to confirm the integrity of the Keggin anion as well as the acidity, which is the key property for relating structure to activity. The best reaction conditions were established for H(3)PW/C and tested for the other supported catalysts. The obtained polymer was a blend that was characterized as an enantiomeric excess (ee) of as much as 95% L-PLA (PLLA) with a mass average molar mass (M(w)) of approximately 14,900 daltons. The role of H(3)PW in these polymerizations was demonstrated, i.e., without the Keggin acid, only oligomeric units (M(w) < 10,000 daltons) could be obtained. Additionally, inverse relationships between the M(w) of PLA and the enthalpy (–ΔH) of the strongest sites of the catalysts were distinguished, i.e., PLA(Mw-H3PW/C) > PLA(Mw-H3PW/Al2O3) > PLA(Mw-H3PW/SiO2), whereas the acidity (–ΔH) order was as follows: H(3)PW/SiO(2) > H(3)PW/Al(2)O(3) > H(3)PW/C. These findings could be attributed to the correct tuning of strength and the accessibility of the sites to produce longer polymeric chains. Elsevier 2019-05-28 /pmc/articles/PMC6539807/ /pubmed/31193779 http://dx.doi.org/10.1016/j.heliyon.2019.e01810 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Chafran, Liana S. Paiva, Mateus F. França, Juliene O.C. Sales, Maria José A. Dias, Sílvia C.L. Dias, José A. Preparation of PLA blends by polycondensation of D,L-lactic acid using supported 12-tungstophosphoric acid as a heterogeneous catalyst |
title | Preparation of PLA blends by polycondensation of D,L-lactic acid using supported 12-tungstophosphoric acid as a heterogeneous catalyst |
title_full | Preparation of PLA blends by polycondensation of D,L-lactic acid using supported 12-tungstophosphoric acid as a heterogeneous catalyst |
title_fullStr | Preparation of PLA blends by polycondensation of D,L-lactic acid using supported 12-tungstophosphoric acid as a heterogeneous catalyst |
title_full_unstemmed | Preparation of PLA blends by polycondensation of D,L-lactic acid using supported 12-tungstophosphoric acid as a heterogeneous catalyst |
title_short | Preparation of PLA blends by polycondensation of D,L-lactic acid using supported 12-tungstophosphoric acid as a heterogeneous catalyst |
title_sort | preparation of pla blends by polycondensation of d,l-lactic acid using supported 12-tungstophosphoric acid as a heterogeneous catalyst |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539807/ https://www.ncbi.nlm.nih.gov/pubmed/31193779 http://dx.doi.org/10.1016/j.heliyon.2019.e01810 |
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