Environmentally friendly adhesives derived from glycerol-based polymers
Source abstract
Abstract
Biodegradable, renewable, and environmentally friendly glycerol-based wood adhesives were synthesized through polycondensation reaction between dicarboxylic acids (sebacic and citric acid) and glycerol using different molar ratios, i.e. poly(glycerol sebacate) – PGS, poly(glycerol citrate-co-sebacate) – PGCS, and poly(glycerol citrate) – PGC. Thermal properties of the synthesized polymers were evaluated after cross-linking. Results showed that thermal stability was influenced by polymer molecular structure, being lower for PGC due to the presence of quaternary carbons of citric acid. Differential scanning calorimetry analyses showed an intermediate glass transition for the copolymer in comparison with homopolymers. Tensile shear strength tests showed that the presence of citric acid in the polymer improves adhesion and reduces adhesive flexibility, contrary to what happens to polymers with sebacic acid. This behavior was also proved through morphological analyses of the fracture surface. Adhesives with tailor-made properties were produced from glycerol, opening up new revenues for a by-product of the biodiesel production chain.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: biodegradable polymer synthesis and properties · Lignin and Wood Chemistry · Polymer crystallization and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Engineering (DEMAT), Materials and Biosystems Laboratory (LAMAB), Federal University of Paraíba (UFPB), João Pessoa, Brazil
Department of Engineering (DEG), Federal University of Lavras (UFLA), Lavras, Brazil
Department of Forest Sciences (DCF), Federal University of Lavras (UFLA), Lavras, Brazil
Laboratory of composites and Adhesives (LADES), Federal Center for Technological Education (CEFET-RJ), Rio de Janeiro, Brazil
References (30)
Show source-provided references
1. 10.1016/j.rser.2012.01.05410.1016/j.rser.2012.01.054 ↗
2. 10.1016/j.rser.2009.07.01710.1016/j.rser.2009.07.017 ↗
3. 10.1016/S0961-9534(97)10028-910.1016/S0961-9534(97)10028-9 ↗
4. 10.1016/j.rser.2013.06.01710.1016/j.rser.2013.06.017 ↗
5. 10.1016/j.apenergy.2009.10.00610.1016/j.apenergy.2009.10.006 ↗
6. Pagliaro M · 201010.1039/9781849731089 ↗
7. 10.1002/9783527632534.ch110.1002/9783527632534.ch1 ↗
8. 10.1016/j.indcrop.2012.11.02110.1016/j.indcrop.2012.11.021 ↗
9. 10.1016/j.indcrop.2014.04.04110.1016/j.indcrop.2014.04.041 ↗
10. 10.1016/j.carbpol.2011.04.00310.1016/j.carbpol.2011.04.003 ↗
11. 10.1016/j.ijadhadh.2015.02.00410.1016/j.ijadhadh.2015.02.004 ↗
12. 10.1179/2042645314Y.000000007510.1179/2042645314Y.0000000075 ↗
13. 10.1016/j.porgcoat.2010.08.01710.1016/j.porgcoat.2010.08.017 ↗
14. 10.1177/09673911130210070610.1177/096739111302100706 ↗
15. 10.1002/app.3277010.1002/app.32770 ↗
16. 10.1016/j.biombioe.2011.09.01210.1016/j.biombioe.2011.09.012 ↗
17. 10.1016/j.ijadhadh.2011.06.01210.1016/j.ijadhadh.2011.06.012 ↗
18. 10.1007/s10924-014-0643-110.1007/s10924-014-0643-1 ↗
19. 10.1002/047147875X10.1002/047147875X ↗
20. ASTM International (ASTM) · 2020
21. 10.1016/j.eurpolymj.2014.12.00810.1016/j.eurpolymj.2014.12.008 ↗
22. 10.15446/dyna.v82n190.4271810.15446/dyna.v82n190.42718 ↗
23. 10.1080/17518253.2014.99181010.1080/17518253.2014.991810 ↗
24. 10.1016/j.matlet.2007.11.04210.1016/j.matlet.2007.11.042 ↗
25. de Paoli M. · 2008
26. Da Silva LFM · 2007
27. 10.1002/app.3666910.1002/app.36669 ↗
28. 10.1016/j.ijadhadh.2013.03.01310.1016/j.ijadhadh.2013.03.013 ↗
29. Berube MA · J Polym Environ · 2012 · 37 · 1051
30. 10.1016/j.progpolymsci.2012.02.00110.1016/j.progpolymsci.2012.02.001 ↗