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. 2024 Sep 14;16(18):2602.
doi: 10.3390/polym16182602.

Bio-Epoxy Resins Based on Lignin and Tannic Acids as Wood Adhesives-Characterization and Bonding Properties

Affiliations

Bio-Epoxy Resins Based on Lignin and Tannic Acids as Wood Adhesives-Characterization and Bonding Properties

Ivana Gavrilović-Grmuša et al. Polymers (Basel). .

Abstract

The possibility of producing and designing bio-epoxides based on the natural polyphenol lignin/epoxidized lignin and tannic acids for application as wood adhesives is presented in this work. Lignin and tannic acids contain numerous reactive hydroxyl phenolic moieties capable of being efficiently involved in the reaction with commercial epoxy resins as a substitute for commercial, non-environmentally friendly, toxic amine-based hardeners. Furthermore, lignin was epoxidized in order to obtain an epoxy lignin that can be a replacement for diglycidyl ether bisphenol A (DGEBA). Cross-linking of bio-epoxy epoxides was investigated via FTIR spectroscopy and their prospects for wood adhesive application were evaluated. This study determined that the curing reaction of epoxy resin can be conducted using lignin/epoxy lignin or tannic acid. Tensile shear strength testing results showed that lignin and tannic acid can effectively replace amine hardeners in epoxy resins. Examination of the failure of the samples showed that all samples had a 100% fracture through the wood. All samples of bio-epoxy adhesives displayed significant tensile shear strength in the range of 5.84-10.87 MPa. This study presents an innovative approach to creating novel cross-linked networks of eco-friendly and high-performance wood bio-adhesives.

Keywords: bio-epoxides; bio-hardener; epoxy lignin; lignin; tannic acid; tensile shear strength.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Cross-linking reactions of tannic acids (TA), Kraft lignin (AKL), and epoxy-modified lignin (EL) with ERs.
Figure 2
Figure 2
Mechanism of lignin epoxidation reaction by epichlorohydrin in alkaline conditions to obtain epoxy lignin (EL).
Figure 3
Figure 3
FTIR spectra of the (a) normalized FTIR (b) raw materials and (c) cured control epoxy and TA/L bio-epoxy adhesives.
Figure 4
Figure 4
Mechanism of the crosslinking of DGEBA, epoxy lignin, and amino hardener during curing.
Figure 5
Figure 5
Mechanism of the crosslinking of epoxy lignin and tannic acid during curing.
Figure 6
Figure 6
(a) preparing the samples for tensile shear strength determination; (b) samples prepared and conditioned for tensile shear strength determination; (c) joint sample after tensile shear testing that have undergone a 100% fracture through the wood.
Figure 7
Figure 7
Tensile shear strength results for different adhesive blends.
Figure 8
Figure 8
(a) ER-AH120; (b) ER-TA10; (c) ER-TA-EL10; and (d) ER-TA-L10.

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