Abstract

Kraft lignin, a side-product of the paper industry, is considered an attractive feedstock for the production of biorenewable chemicals. However, its recalcitrant nature and sulfur content render catalytic conversions challenging. This study demonstrates the efficacy of noble metal-based catalysts for the production of a lignin oil enriched in alkylphenolic and aromatic compounds, by a catalytic hydrotreatment of Kraft lignin without the use of an external solvent. Eight commercially available catalysts were evaluated using four different metals (Ru, Pt, Pd, Rh) on two supports (activated carbon and Al2O3). The product oils were extensively analyzed by means of GPC, GCxGC-FID, GC–MS-FID, and elemental analysis. The catalysts were characterized by various techniques (N2 physisorption, NH3-TPD, XRD and TEM) before and after reaction, and their physico-chemical properties were correlated with catalytic performance. Al2O3 as support gave better results than carbon as support in terms of lignin oil yield and composition, due to a combination of higher total acidity, mildly acidic sites and a mesoporous structure. The metallic phase also significantly affected product distribution. The best results were obtained using a Rh/Al2O3 catalyst, resulting in a lignin oil yield of 36.3 wt% on a lignin intake and a total monomer yield of 30.0 wt% on lignin intake including 15.3 wt% of alkylphenolic and 7.9 wt% of aromatic compounds, and with a sulfur content <0.01 wt%.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.