Chemical and Mechanical Characterization of Licorice Root and Palm Leaf Waste Incorporated into Poly(urethane-acrylate) (PUA).


Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
19 Dec 2021
Historique:
received: 19 11 2021
revised: 13 12 2021
accepted: 16 12 2021
entrez: 24 12 2021
pubmed: 25 12 2021
medline: 15 2 2022
Statut: epublish

Résumé

A poly(urethane-acrylate) polymer (PUA) was synthesized, and a sufficiently high molecular weight starting from urethane-acrylate oligomer (UAO) was obtained. PUA was then loaded with two types of powdered ligno-cellulosic waste, namely from licorice root and palm leaf, in amounts of 1, 5 and 10%, and the obtained composites were chemically and mechanically characterized. FTIR analysis of final PUA synthesized used for the composite production confirmed the new bonds formed during the polymerization process. The degradation temperatures of the two types of waste used were in line with what observed in most common natural fibers with an onset at 270 °C for licorice waste, and at 290 °C for palm leaf one. The former was more abundant in cellulose (44% vs. 12% lignin), whilst the latter was richer in lignin (30% vs. 26% cellulose). In the composites, only a limited reduction of degradation temperature was observed for palm leaf waste addition and some dispersion issues are observed for licorice root, leading to fluctuating results. Tensile performance of the composites indicates some reduction with respect to the pure polymer in terms of tensile strength, though stabilizing between data with 5 and 10% filler. In contrast, Shore A hardness of both composites slightly increases with higher filler content, while in stiffness-driven applications licorice-based composites showed potential due to an increase up to 50% compared to neat PUA. In general terms, the fracture surfaces tend to become rougher with filler introduction, which indicates the need for optimizing interfacial adhesion.

Identifiants

pubmed: 34946764
pii: molecules26247682
doi: 10.3390/molecules26247682
pmc: PMC8705998
pii:
doi:

Substances chimiques

Acrylic Resins 0
Polymers 0
Polyurethanes 0
urethane acrylate 0
Cellulose 9004-34-6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Références

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pubmed: 33131999
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ACS Omega. 2019 Jul 23;4(7):12505-12511
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Materials (Basel). 2017 Jul 28;10(8):
pubmed: 28773234

Auteurs

Serena Gabrielli (S)

ChIP Building, School of Science and Technology, Università degli Studi di Camerino, Via Madonna delle Carceri, 62032 Camerino, Italy.

Genny Pastore (G)

ChIP Building, School of Science and Technology, Università degli Studi di Camerino, Via Madonna delle Carceri, 62032 Camerino, Italy.

Francesca Stella (F)

ChIP Building, School of Science and Technology, Università degli Studi di Camerino, Via Madonna delle Carceri, 62032 Camerino, Italy.

Enrico Marcantoni (E)

ChIP Building, School of Science and Technology, Università degli Studi di Camerino, Via Madonna delle Carceri, 62032 Camerino, Italy.

Fabrizio Sarasini (F)

Department of Chemical Engineering Materials Environment, Sapienza-Università di Roma, Via Eudossiana 18, 00184 Roma, Italy.

Jacopo Tirillò (J)

Department of Chemical Engineering Materials Environment, Sapienza-Università di Roma, Via Eudossiana 18, 00184 Roma, Italy.

Carlo Santulli (C)

Geology Section, School of Science and Technology, Università degli Studi di Camerino, Via Gentile III da Varano 7, 62032 Camerino, Italy.

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Classifications MeSH