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Rigid Oligomer from Lignin in Designing of Tough, Self-Healing Elastomers
Author(s) -
Mengmeng Cui,
Ngoc A. Nguyen,
Peter V. Bonnesen,
David Uhrig,
Jong K. Keum,
Amit K. Naskar
Publication year - 2018
Publication title -
acs macro letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.966
H-Index - 92
ISSN - 2161-1653
DOI - 10.1021/acsmacrolett.8b00600
Subject(s) - oligomer , materials science , elastomer , lignin , adhesive , self healing hydrogels , self healing , solvent , polymer , epoxy , polymer chemistry , composite material , organic chemistry , chemistry , medicine , alternative medicine , pathology , layer (electronics)
Converting lignin into well-defined compounds is often challenged by structural complexation and inorganic contamination induced by the pulping process. In this report, instead of breaking down lignin into small molecules, we extracted a uniform and rigid oligomer from the lignin waste stream. The multifunctional polyphenol oligomer containing carboxylic acid, alcohol, and phenol groups is highly reactive and brings stiffness into the material matrix. Tough and self-healing elastomers are economically prepared from this oligomer by a reaction with epoxy-terminated polyethylene glycol, without needing any solvent. Specifically, the polyaromatic backbone's rigidity enhances the elastomer's toughness, and the multiple polar substituents form a network of hydrogen bonding that heals the elastomer. Many other applications, including adhesives, hydrogels, coating, and metal scavengers, are envisioned based on this oligomer's unique properties.

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