Asset Details
Do you wish to reserve the book?
Toward a Green Polymerization of Lignin‐Derived Monomers in Ethyl Lactate Solution or Aqueous Emulsion
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Toward a Green Polymerization of Lignin‐Derived Monomers in Ethyl Lactate Solution or Aqueous Emulsion
Do you wish to request the book?
Toward a Green Polymerization of Lignin‐Derived Monomers in Ethyl Lactate Solution or Aqueous Emulsion
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Journal Article
Toward a Green Polymerization of Lignin‐Derived Monomers in Ethyl Lactate Solution or Aqueous Emulsion
2026
Overview
Novel biobased polymers based on lignin building blocks are synthesized and systematically characterized. The three prominent aromatic aldehydes that can be obtained from oxidative degradation of lignin, namely p‐hydroxybenzaldehyde (H), vanillin (V), and syringaldehyde (S), are chemically modified into radically polymerizable styrenic monomers presenting either a methoxy or butoxy (‐OBu) group at the para‐position. The transformation of these molecules is accomplished and optimized individually on each compound. Subsequently, polymers are successfully prepared by free radical polymerization in homogeneous conditions (in solution using ethyl lactate as green solvent) and in heterogeneous conditions (in aqueous emulsion using a biosourced surfactant). Novel polymeric materials with high thermal stability and a glass transition temperature (Tg) tunable between 40°C and 110°C are obtained, depending on the monomer used.
Publisher
John Wiley & Sons, Inc,Wiley-VCH Verlag,Wiley-VCH
Subject
