Reversible Fe3+-induced urushi organogels in gamma butyrolactone

Authors
Hur, JihyeonKim, MinseokKim, Jun TaeYang, EunyeongHwang, Seung SangWon, Jongok
Issue Date
2024-01
Publisher
Elsevier BV
Citation
International Journal of Adhesion and Adhesives, v.128
Abstract
A multinetwork structured urushi organogel was created using low-volatility gamma butyrolactone (GBL) solvent and Fe3+ ions. The urushi organogels were fabricated through chemical crosslinking with the oxidative poly-merization of urushiol as well as physical crosslinking due to the coordination bonds with Fe3+ ions in the Fe3+/ urushiol/GBL solution. The role of Fe3+ ions is to provide physical crosslinking sites via the coordination bond with the catechol functional moiety of urushiol and also to serve as the catalysts for the polymerization of urushiol. The gelation and characteristics of urushi organogels in GBL with different amounts of Fe3+ ions were investigated. The formation of urushi organogel by chemical crosslinking and physical coordination crosslinking was investigated by FT-IR, Raman spectroscopy and X-ray photoelectron spectroscopy.The presence of a physical coordination bond between the Fe3+ ion and the catechol moiety of urushiol provides reversible adhesive properties, which provide consistent tensile strength after reattaching the urushi organogel film. The stretchability as well as the reversibility in mechanical strength can provide the possibility for various applications of eco-friendly natural urushi. This research provides not only a method to prepare multinetwork natural urushi organogels using Fe3+ ions but also the great possibility of expanding the appli-cation area of natural urushi(ol)s.
Keywords
JANUS COMPOSITE-PARTICLES; UV-INDUCED POLYMERIZATION; CROSS-LINKING; EQUILIBRIA; OXIDATION; IRON(III); MEMBRANES; ADHESIVE; KINETICS; Natural polymer; Organogel; Urushiol; Reversibility; Multinetwork gel; Renewable resource
ISSN
0143-7496
URI
https://pubs.kist.re.kr/handle/201004/112967
DOI
10.1016/j.ijadhadh.2023.103534
Appears in Collections:
KIST Article > 2024
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