Selective depolymerization of industrial lignin-containing stillage obtained from cellulosic bioethanol processing

Reductive depolymerization of lignin-containing stillage (LA lignin) from 2nd generation bioethanol industrial plants have been studied over two different families of catalysts: conventional porous Ru catalysts supported on ZrO2 or activated carbon, and 1-dimensional Ru catalysts supported on multi-...

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Bibliographic Details
Published inFuel processing technology Vol. 173; pp. 165 - 172
Main Authors Gómez-Monedero, Beatriz, Pilar Ruiz, M., Bimbela, Fernando, Faria, Jimmy
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.05.2018
Elsevier Science Ltd
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Summary:Reductive depolymerization of lignin-containing stillage (LA lignin) from 2nd generation bioethanol industrial plants have been studied over two different families of catalysts: conventional porous Ru catalysts supported on ZrO2 or activated carbon, and 1-dimensional Ru catalysts supported on multi-walled carbon nanotubes (MWCNT). The lignin depolymerization degree using conventional porous catalysts resulted in values of 42 and 53%, for Ru/ZrO2 and Ru/C, respectively. Strikingly, when using 1D-supported catalysts (Ru/MWCNT and Ru/ZrO2/MWCNT), the extent of lignin depolymerization measured by 1H13C HSQC NMR, reached values of c.a. 80% of β-O-4 bond disappearance and a reduction of the average molecular weight from 3600 Da to ~ 1900 Da. The higher accessibility of the lignin agglomerates to the 1-D catalyst nanoparticles substantially improves the lignin depolymerization degree, which make this approach of great interest in the production of fine chemicals and fuel additives. [Display omitted] •Lignin stillage has been depolymerized up to 80% of β-O-4 bond disappearance.•Selective depolymerization of β-O-4 ether bonds has been achieved on Ru catalysts.•1-D Ru/MWCNT catalysts show the highest depolymerization extent.•1-D Ru/MWCNT catalysts increase accessibility of the lignin molecules to the catalyst.
ISSN:0378-3820
1873-7188
DOI:10.1016/j.fuproc.2018.01.021