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Synthesis, characterisation, and thermal degradation kinetics of lignin-based polyurethane wood adhesives

dc.contributor.authorHernández-Ramos, Fabio
dc.contributor.authorEsteves, Bruno
dc.contributor.authorCarvalho, Luisa Hora de
dc.contributor.authorLabidi, Jalel
dc.contributor.authorErdocia, Xabier
dc.date.accessioned2025-01-07T13:54:51Z
dc.date.available2025-01-07T13:54:51Z
dc.date.issued2025-01
dc.date.updated2024-12-21T22:00:17Z
dc.description.abstractPolyurethane adhesives are widely employed in a range of industrial applications due to their exceptional bonding strength, flexibility, and chemical resistance. These materials play a crucial role in wood bonding technologies, where their versatility and durability make them ideal for creating strong, long-lasting joints. In this work, Four different polyurethane wood adhesives were synthesised using ligno-based bio-polyols obtained through microwave assisted liquefaction reaction of two wood species (hardwood and softwood) using polyethylene glycol and glycerol as solvents. The reaction conditions used for the synthesis of bio-polyols were optimised in a previous work. The synthesis of polyurethanes was carried out by one-shot method using Tetrahydrofuran (THF) as solvent and MDI as diisocyanate employing different NCO:OH ratios (2.0:1, 2.5:1, and 3.0:1). The chemical structure of polyurethanes was determined through ATR-FTIR and the shear strength was analysed using Automated Bonding Evaluation System (ABES) employing beech veneer strips. Through ABES it was concluded that an NCO:OH ratio of 2.5:1 was the formulation that showed the best shear strength for a pressing time of 120 s. Employing this ratio and the same synthesis procedure, two new polyurethanes were synthesised with the bio-polyols obtained using crude glycerol instead commercial glycerol. Finally, a study of thermal degradation kinetics employing the Ozawa–Flynn–Wall (OFW) and Kissinger–Akahira–Sunose (KAS) isoconversional methods of the polyurethanes synthesised with an NCO:OH ratio of 2.5:1 was carried out. On the one hand, the Ea of each system were estimated for the different α ratios, obtaining slightly higher values for the adhesives produced using commercial glycerol than crude glycerol. In addition, the pre-exponential factor was determined, enabling an estimation of the lifetime of the polymers. This study highlights demonstrated that crude glycerol could replace commercial glycerol without compromising adhesive properties. The findings revealed that the lignin source significantly influences the adhesive's characteristics and stability, while addressing challenges in achieving industrial viability remains essential for broader application.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1016/j.ijadhadh.2024.103889pt_PT
dc.identifier.issn0143-7496
dc.identifier.slugcv-prod-4244632
dc.identifier.urihttp://hdl.handle.net/10400.19/8717
dc.language.isoporpt_PT
dc.peerreviewedyespt_PT
dc.subjectLigninpt_PT
dc.subjectBio-polyolpt_PT
dc.subjectPolyurethanept_PT
dc.subjectAdhesivespt_PT
dc.subjectThermal degradation kineticspt_PT
dc.titleSynthesis, characterisation, and thermal degradation kinetics of lignin-based polyurethane wood adhesivespt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.titleInternational Journal of Adhesion and Adhesivespt_PT
oaire.citation.volume136pt_PT
person.familyNameEsteves
person.givenNameBruno
person.identifier2119255
person.identifier.ciencia-id521B-63A7-B248
person.identifier.orcid0000-0001-6660-3128
person.identifier.ridC-2173-2012
person.identifier.scopus-author-id57202554441
rcaap.cv.cienciaid521B-63A7-B248 | Bruno Miguel Morais Lemos Esteves
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicationa3351493-41e8-4758-acae-39e3382d0b04
relation.isAuthorOfPublication.latestForDiscoverya3351493-41e8-4758-acae-39e3382d0b04

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