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.

Chemical and mechanical characterization of licorice root and palm leaf waste incorporated into poly(Urethane-acrylate) (pua) / Gabrielli, S.; Pastore, G.; Stella, F.; Marcantoni, E.; Sarasini, F.; Tirillo', J.; Santulli, C.. - In: MOLECULES. - ISSN 1420-3049. - 26:24(2021). [10.3390/molecules26247682]

Chemical and mechanical characterization of licorice root and palm leaf waste incorporated into poly(Urethane-acrylate) (pua)

Sarasini F.;Tirillo' J.;
2021

Abstract

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.
2021
licorice root; lignocellulosic materials; mechanical properties; oil palm leaf; poly(urethane-acrylate); thermal properties
01 Pubblicazione su rivista::01a Articolo in rivista
Chemical and mechanical characterization of licorice root and palm leaf waste incorporated into poly(Urethane-acrylate) (pua) / Gabrielli, S.; Pastore, G.; Stella, F.; Marcantoni, E.; Sarasini, F.; Tirillo', J.; Santulli, C.. - In: MOLECULES. - ISSN 1420-3049. - 26:24(2021). [10.3390/molecules26247682]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1599823
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