News Release

Nucleophilic amino acids as a renewable alternative to petrochemically-derived amines in glycerol epoxy resins

The curing behavior of amino acids and glycerol epoxy resins was examined, as well as the reaction conditions required for the reaction of amino, carboxyl, and hydroxyl groups with epoxy groups and the extent of the reaction

Peer-Reviewed Publication

Journal of Bioresources and Bioproducts

The Appearance of cured resins of GER-Lys, GER-Glu, GER-Ser, and GER-Leu and the water-soluble epoxy resin and hardeners used in this study. CREDIT: THE AUTHORS

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This study explored Lys, Ser, Leu, and Glu as potential curing agents for epoxy resins as amino acids.

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Credit: Changlei Xia, College of Materials Science and Engineering, Nanjing Forestry University, Nanjing 210037, China, changlei.xia@njfu.edu.cn

Epoxide exhibits superior crosslinking properties, thereby enhancing the bonding performance of soy protein adhesives owing to its elevated glass transition temperature and mechanical property. Commercia resins are mainly derived from petroleum and contain the toxic chemical bisphenol A. Although commercial hardeners have been extensively utilized, these systems still have particular environmental concerns that have been become particularly notable in recent years. Amino acids, a bio-based epoxy curing agent with amino and carboxyl groups, are another potential curing agent. Water-soluble epoxy resins cured with lysine (Lys), glutamic acid (Glu), leucine (Leu), and serine (Ser) as amino acids were investigated. The results showed that the water-soluble epoxy resin (glycerol epoxy resins, GER) was cured with Lys and Glu after reacting. The potential of Lys and Glu alternatives for petrochemical amines is demonstrated and provides promising opportunities for industrial application.

 

 

DOI

https://doi.org/10.1016/j.jobab.2024.01.003

Original Source URL

https://www.sciencedirect.com/science/article/pii/S2369969824000148

Journal

Journal of Bioresources and Bioproducts


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