Product tunable behavior of carbon nanotubes-supported Ni-Fe catalysts for guaiacol hydrodeoxygenation

Bimetallic Ni-Fe nanoparticles supported on carbon nanotubes (CNTs) are prepared and evaluated for the catalytic hydrodeoxygenation (HDO) of a lignin-derived model compound guaiacol. Appropriate combination of Ni and Fe affords high activity and significantly enhances selectivity to cyclohexane or phenol, whereas monometallic Ni and Fe catalysts display poor activities or Selectivities. The product tunable behavior of guaiacol HDO is found to be dependent on Ni/Fe atomic ratios. Cyclohexane and phenol are the Major products over Ni-5-Fe-1/CNT with Ni/Fe atomic ratio at 5/1 and Ni-1-Fe-5/CNT with Ni/Fe atomic ratio at 1/5, respectively. Characterization results confirm that Ni-Fe alloys are formed and elicit synergistic effects on the HDO performance. The selectivity-switchable performance of Ni-Fe/CNT can be assigned to the synergism between Ni domains, where H-2 can be easily activated, and Fe domains, which exhibited strong oxophilicity. The bimetallic catalysts give an enhanced stability without significant sintering of metal nanoparticles, while the monometallic catalysts show obvious deactivation due to the agglomeration of metal, nanoparticles. Further results reveal that the conversion of guaiacol depends on not only the chemical state but also the size of the metallic nanoparticles. The catalysts with appropriate Ni/Fe atomic ratio and smaller particle perform better hydrogenolysis Of C-O bonds, resulting in high selectivity to cyclohexane or phenol. (C) 2016 Elsevier B.V. All rights reserved.