Advertisement

If you have an ACS member number, please enter it here so we can link this account to your membership. (optional)

ACS values your privacy. By submitting your information, you are gaining access to C&EN and subscribing to our weekly newsletter. We use the information you provide to make your reading experience better, and we will never sell your data to third party members.

ENJOY UNLIMITED ACCES TO C&EN

Environment

Nickel catalyst converts tough plant lignin into valuable chemicals

Waste from the grass Miscanthus yields compounds useful in the flavor and fragrance industry

by Deirdre Lockwood
March 14, 2016 | A version of this story appeared in Volume 94, Issue 11

[+]Enlarge
Credit: Sponner/Shutterstock
Using a nickel catalyst, researchers converted lignin from Miscanthus grass into phenolic compounds, such as propylsyringol and ferulic acid methyl esters, that can be converted into valuable flavor and fragrance compounds.
Photo of a Miscanthus crop with structures of compounds that can be derived from lignin.
Credit: Sponner/Shutterstock
Using a nickel catalyst, researchers converted lignin from Miscanthus grass into phenolic compounds, such as propylsyringol and ferulic acid methyl esters, that can be converted into valuable flavor and fragrance compounds.

To make fuels and chemicals from biomass, producers typically use the sugar-containing cellulose components. But first they must remove the surrounding lignin, a hardy phenolic biopolymer that helps support plant structure. Researchers have been looking for viable methods to crack apart the lignin into useful chemical intermediates, with some success coming from using precious-metal catalysts. A new study shows that an inexpensive nickel catalyst can transform 68% of lignin from the grass Miscanthus into aromatic compounds, while preserving residual plant sugars for subsequent conversion to fuels and other chemicals (ACS Sustainable Chem. Eng. 2016, DOI: 10.1021/acssuschemeng.5b01776). Mahdi M. Abu-Omar of Purdue University and colleagues combine 1 g of milled Miscanthus with 45 mL of methanol in a reactor containing nickel dispersed on activated carbon. The researchers place the catalyst in a microporous stainless steel cage so that the nickel can contact phenolic oligomers that form as the lignin breaks apart under high pressure and temperature, while keeping the catalyst separate from the carbohydrate residue left behind by the reaction. The catalyst deoxygenates the oligomers, turning them into a range of compounds, including dihydroeugenol, propylsyringol, and ferulic acid methyl ester, which can be used to make vanillin, the principal component of vanilla flavoring. The team further treats the residue with an iron chloride catalyst to make furfural and levulinic acid—products that can be used to make biofuels or other chemicals.

Article:

This article has been sent to the following recipient:

0 /1 FREE ARTICLES LEFT THIS MONTH Remaining
Chemistry matters. Join us to get the news you need.