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Ambient-pressure and low-temperature upgrading of lignin bio-oil to hydrocarbons using a hydrogen buffer catalytic system

Abstract

Catalytic hydrodeoxygenation is an essential step for bio-oil upgrading. However, hydrodeoxygenation usually requires a high hydrogen pressure and high temperature due to the good stability of the C–O bonds. Here we report an effective multiphase hydrodeoxygenation of lignin-based bio-oil at temperatures <100 °C and hydrogen pressures <1 atm using a synergetic catalyst system that consists of a low redox potential H4SiW12O40 (SiW12) and suspended Pt-on-carbon (Pt/C) particles. We propose that SiW12 plays three critical roles in bio-oil hydrodeoxygenation. First, it quickly oxidizes the H2 gas to form reduced SiW12 in the presence of Pt/C. Second, it transfers both electrons and H+ ions to the bulk phase to form active H* or H2 on the Pt/C surface. Third, the formation of the oxonium ion in a SiW12 superacid solution reduces the deoxygenation energy. The SiW12-enhanced proton-transfer hydrodeoxygenation mechanism is supported by density functional theory computations. As a result of the hydrogen buffer and acidic effect, up to a 90% yield of hydrocarbons (cyclohexane, benzene and their derivatives) was achieved from the hydrodeoxygenation of phenol and its derivatives.

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Fig. 1: Illustration of hydrogen-buffer-improved bio-oil upgrading.
Fig. 2: The hydrogen buffer effect and HDO performance of the SiW12 and Pt/C catalyst system.
Fig. 3: HDO of phenol and guaiacol.
Fig. 4: Proposed mechanism of SiW12-induced HDO.
Fig. 5: Upgrading of different functional-group-substituted compounds under mild conditions.
Fig. 6: Three possible pathways for defunctionalization of the –OCH3 group using anisole as a model compound.

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Data availability

The authors declare that the data supporting the findings of this study are available in the Article and Supplementary Information. Source data are provided with this paper.

References

  1. Armstrong, R. C. et al. The frontiers of energy. Nat. Energy 1, 15020 (2016).

    Google Scholar 

  2. Liu, B. & Rajagopal, D. Life-cycle energy and climate benefits of energy recovery from wastes and biomass residues in the United States. Nat. Energy 4, 700–708 (2019).

    Google Scholar 

  3. Savage, N. Fuel options: the ideal biofuel. Nature 474, S9–S11 (2011).

    Google Scholar 

  4. Kunkes, E. L. et al. Catalytic conversion of biomass to monofunctional hydrocarbons and targeted liquid-fuel classes. Science 322, 417–421 (2008).

    Google Scholar 

  5. Ragauskas, A. J. et al. Lignin valorization: improving lignin processing in the biorefinery. Science 344, 1246843 (2014).

    Google Scholar 

  6. Duan, H. et al. Hydrodeoxygenation of water-insoluble bio-oil to alkanes using a highly dispersed Pd–Mo catalyst. Nat. Commun. 8, 591 (2017).

    Google Scholar 

  7. Xia, Q. et al. Direct hydrodeoxygenation of raw woody biomass into liquid alkanes. Nat. Commun. 7, 11162 (2016).

    Google Scholar 

  8. Saidi, M. et al. Upgrading of lignin-derived bio-oils by catalytic hydrodeoxygenation. Energ. Environ. Sci. 7, 103–129 (2014).

    Google Scholar 

  9. Lin, Z., Chen, R., Qu, Z. & Chen, J. G. Hydrodeoxygenation of biomass-derived oxygenates over metal carbides: from model surfaces to powder catalysts. Green Chem. 20, 2679–2696 (2018).

    Google Scholar 

  10. Mu, W., Ben, H., Ragauskas, A. & Deng, Y. Lignin pyrolysis components and upgrading—technology review. BioEnergy Res. 6, 1183–1204 (2013).

    Google Scholar 

  11. Jing, Y., Dong, L., Guo, Y., Liu, X. & Wang, Y. Chemicals from lignin: a review of the catalytic conversion involving hydrogen. ChemSusChem 13, 1–19 (2020).

    Google Scholar 

  12. Shafaghat, H., Rezaei, P. S. & Daud, W. M. A. W. Effective parameters on selective catalytic hydrodeoxygenation of phenolic compounds of pyrolysis bio-oil to high-value hydrocarbons. RSC Adv. 5, 103999–104042 (2015).

    Google Scholar 

  13. Wang, H., Male, J. & Wang, Y. Recent advances in hydrotreating of pyrolysis bio-oil and its oxygen-containing model compounds. ACS Catal. 3, 1047–1070 (2013).

    Google Scholar 

  14. Pritchard, J., Filonenko, G. A., van Putten, R., Hensen, E. J. M. & Pidko, E. A. Heterogeneous and homogeneous catalysis for the hydrogenation of carboxylic acid derivatives: history, advances and future directions. Chem. Soc. Rev. 44, 3808–3833 (2015).

    Google Scholar 

  15. Kozhevnikov, I. V. Advances in catalysis by heteropolyacids. Russian Chem. Rev. 56, 811–825 (1987).

    Google Scholar 

  16. Rausch, B., Symes, M. D., Chisholm, G. & Cronin, L. Decoupled catalytic hydrogen evolution from a molecular metal oxide redox mediator in water splitting. Science 345, 1326–1330 (2014).

    Google Scholar 

  17. Yang, G. et al. The nature of hydrogen adsorption on platinum in the aqueous phase. Angew. Chem. Int. Ed. 58, 3527–3532 (2019).

    Google Scholar 

  18. Singh, N. et al. Impact of pH on aqueous-phase phenol hydrogenation catalyzed by carbon-supported Pt and Rh. ACS Catal. 9, 1120–1128 (2019).

    Google Scholar 

  19. Zhao, C., He, J., Lemonidou, A. A., Li, X. & Lercher, J. A. Aqueous-phase hydrodeoxygenation of bio-derived phenols to cycloalkanes. J. Catal. 280, 8–16 (2011).

    Google Scholar 

  20. Güvenatam, B., Kurşun, O., Heeres, E. H. J., Pidko, E. A. & Hensen, E. J. M. Hydrodeoxygenation of mono- and dimeric lignin model compounds on noble metal catalysts. Catal. Today 233, 83–91 (2014).

    Google Scholar 

  21. Ohta, H. et al. Low temperature hydrodeoxygenation of phenols under ambient hydrogen pressure to form cyclohexanes catalysed by Pt nanoparticles supported on H-ZSM-5. Chem. Commun. 51, 17000–17003 (2015).

    Google Scholar 

  22. Alshehri, F., Feral, C., Kirkwood, K. & Jackson, S. D. Low temperature hydrogenation and hydrodeoxygenation of oxygen-substituted aromatics over Rh/silica: part 1: phenol, anisole and 4-methoxyphenol. React. Kinet. Mech. Catal. 128, 23–40 (2019).

    Google Scholar 

  23. Chen, L., Fink, C., Fei, Z., Dyson, P. J. & Laurenczy, G. An efficient Pt nanoparticle–ionic liquid system for the hydrodeoxygenation of bio-derived phenols under mild conditions. Green Chem. 19, 5435–5441 (2017).

    Google Scholar 

  24. Ohta, H. et al. Surface modification of a supported Pt catalyst using ionic liquids for selective hydrodeoxygenation of phenols into arenes under mild conditions. Chem. Eur. J. 25, 14762–14766 (2019).

    Google Scholar 

  25. He, Z. & Wang, X. Hydrodeoxygenation of model compounds and catalytic systems for pyrolysis bio-oils upgrading. Catal. Sustain. Energy 1, 28–52 (2012).

    Google Scholar 

  26. Long, W. et al. Different crystal form titania supported ruthenium nanoparticles for liquid phase hydrodeoxygenation of guaiacol. J. Nanosci. Nanotechnol. 18, 8426–8436 (2018).

    Google Scholar 

  27. Si, Z., Zhang, X., Wang, C., Ma, L. & Dong, R. An overview on catalytic hydrodeoxygenation of pyrolysis oil and its model compounds. Catalysts 7, 169 (2017).

    Google Scholar 

  28. Mäki-Arvela, P. & Murzin, Y. D. Hydrodeoxygenation of lignin-derived phenols: from fundamental studies towards industrial applications. Catalysts 7, 265 (2017).

    Google Scholar 

  29. Garcia-Pintos, D., Voss, J., Jensen, A. D. & Studt, F. Hydrodeoxygenation of phenol to benzene and cyclohexane on Rh(111) and Rh(211) surfaces: insights from density functional theory. J. Phys. Chem. C 120, 18529–18537 (2016).

    Google Scholar 

  30. Wang, M., Shi, H., Camaioni, D. M. & Lercher, J. A. Palladium-catalyzed hydrolytic cleavage of aromatic C−O bonds. Angew. Chem. Int. Ed. 56, 2110–2114 (2017).

    Google Scholar 

  31. Yoon, Y., Rousseau, R., Weber, R. S., Mei, D. & Lercher, J. A. First-principles study of phenol hydrogenation on Pt and Ni catalysts in aqueous phase. J. Am. Chem. Soc. 136, 10287–10298 (2014).

    Google Scholar 

  32. Liu, D. et al. Competition and cooperation of hydrogenation and deoxygenation reactions during hydrodeoxygenation of phenol on Pt(111). J. Phys. Chem. C 121, 12249–12260 (2017).

    Google Scholar 

  33. Hensley, A. J. R., Wang, Y. & McEwen, J.-S. Phenol deoxygenation mechanisms on Fe(110) and Pd(111). ACS Catal. 5, 523–536 (2015).

    Google Scholar 

  34. Jordan, K. D., Michejda, J. A. & Burrow, P. D. Electron transmission studies of the negative ion states of substituted benzenes in the gas phase. J. Am. Chem. Soc. 98, 7189–7191 (1976).

    Google Scholar 

  35. Jiang, G., Nowakowski, D. J. & Bridgwater, A. V. Effect of the temperature on the composition of lignin pyrolysis products. Energy Fuel. 24, 4470–4475 (2010).

    Google Scholar 

  36. Staš, M., Chudoba, J., Kubička, D., Blažek, J. & Pospíšil, M. Petroleomic characterization of pyrolysis bio-oils: a review. Energy Fuel 31, 10283–10299 (2017).

    Google Scholar 

  37. Pourzolfaghar, H., Abnisa, F., Wan Daud, W. M. A. & Aroua, M. K. Atmospheric hydrodeoxygenation of bio-oil oxygenated model compounds: ae review. J. Anal. Appl. Pyrol. 133, 117–127 (2018).

    Google Scholar 

  38. Zhang, C. et al. Promoting lignin depolymerization and restraining the condensation via an oxidation−hydrogenation strategy. ACS Catal. 7, 3419–3429 (2017).

    Google Scholar 

  39. Kresse, G. & Furthmüller, J. Efficient iterative schemes for ab initio total-energy calculations using a plane-wave basis set. Phys. Rev. B 54, 11169–11186 (1996).

    Google Scholar 

  40. Blöchl, P. E. Projector augmented-wave method. Phys. Rev. B 50, 17953–17979 (1994).

    Google Scholar 

  41. Perdew, J. P., Burke, K. & Ernzerhof, M. Generalized gradient approximation made simple. Phys. Rev. Lett. 77, 3865–3868 (1996).

    Google Scholar 

  42. Mathew, K., Sundararaman, R., Letchworth-Weaver, K., Arias, T. A. & Hennig, R. G. Implicit solvation model for density-functional study of nanocrystal surfaces and reaction pathways. J. Chem. Phys. 140, 084106 (2014).

    Google Scholar 

  43. Henkelman, G., Uberuaga, B. P. & Jónsson, H. A climbing image nudged elastic band method for finding saddle points and minimum energy paths. J. Chem. Phys. 113, 9901–9904 (2000).

    Google Scholar 

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Acknowledgements

W.L. thanks the RBI at Georgia Tech for scholarship support.

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Authors and Affiliations

Authors

Contributions

Y.D. and W.L. conceived the project and designed the experiments. W.L. performed the electrochemical measurement and HDO experiments. W.S. and W. Yang helped with the HDO experiments and product analysis by GC. W. You and W.L. conducted the DFT calculations of proton-induced mechanisms. A.K. performed GC–mass spectrometry analysis of the HDO products. Y.G. performed the catalyst characterizations.

Corresponding author

Correspondence to Yulin Deng.

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Supplementary information

Supplementary Information

Supplementary Tables 1–5, Figs. 1–40 and refs. 1–55.

Supplementary Data

Source data for the TOFs of hydrocarbon generation during the phenol hydrodeoxygenation with different Pt-to-phenol ratios.

Source data

Source Data Fig. 3b

Source data for hydrodeoxygenations of phenol (at 75 °C) and guaiacol (at 95 °C) using N2 and H2 mixing gas (total pressure 1 atm).

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Liu, W., You, W., Sun, W. et al. Ambient-pressure and low-temperature upgrading of lignin bio-oil to hydrocarbons using a hydrogen buffer catalytic system. Nat Energy 5, 759–767 (2020). https://doi.org/10.1038/s41560-020-00680-x

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