scholarly journals Biomass Fast Pyrolysis Vapor Upgrading over γ-Alumina, Hydrotalcite, Dolomite and Effect of Na2CO3 Loading: A Pyro Probe GCMS Study

Energies ◽  
2021 ◽  
Vol 14 (17) ◽  
pp. 5397
Author(s):  
Harsha Mysore Prabhakara ◽  
Eddy Bramer ◽  
Gerrit Brem

The influence of γ-alumina, hydrotalcite, dolomite and Na2CO3 loaded γ-alumina, hydrotalcite, dolomite on fast pyrolysis vapor upgrading of beechwood was investigated using an analytical pyro probe-gas chromatography/mass spectrometry instrument (Py-GC/MS) at a temperature of 500 °C. Overall, this research showcased that these catalysts can deoxygenate biomass pyrolysis vapors into a mixture of intermediate compounds which have substantially lower oxygen content. The intermediate compounds are deemed to be suitable for downstream hydrodeoxygenation processes and it also means that hydrogen consumption will be reduced as a result of moderate in-situ deoxygenation. Among the support catalysts, the application of hydrotalcite yielded the best results with the formation of moderately deoxygenated compounds such as light phenols, mono-oxy ketones, light furans and hydrocarbons with a TIC area % of 7.5, 44.8, 9.8 and 9.8, respectively. In addition, acids were considerably reduced. Dolomite was the next most effective catalyst as γ-alumina retained most of the acids and other oxygenates. Na2CO3 loading on γ-alumina had a noticeable effect on eliminating more or less all the acids, enhancing the mono-oxy-ketones and producing lighter furans. In contrast, Na2CO3 loading on dolomite and hydrotalcite did not show a major impact on the composition except for further enhancing the mono-oxy-ketones (e.g., acetone and cyclopentenones). Additionally, in the case of hydrotalcite and γ-alumina, Na2CO3 loading suppressed the formation of hydrocarbons. In this research, the composition of pyrolytic vapors as a result of catalysis is elaborated further under the specific oxygenate groups such as acids, phenolics, furanics, ketones and acids. Further the catalysts were also characterized by BET, XRD and TGA analysis.

Holzforschung ◽  
2014 ◽  
Vol 68 (2) ◽  
pp. 151-155 ◽  
Author(s):  
Daniel J. van de Pas ◽  
Bernadette Nanayakkara ◽  
Ian D. Suckling ◽  
Kirk M. Torr

Abstract Mild hydrogenolysis has been compared with thioacidolysis as a method for degrading lignins in situ and in isolated form before analysis by gas chromatography/mass spectrometry and quantitative 31P nuclear magnetic resonance (NMR) spectroscopy. Both degradation methods gave similar levels of β-aryl ether-linked phenylpropane units that were released as monomers. Degradation by hydrogenolysis generally gave lower levels of total phenylpropane units when analyzed by 31P NMR, especially in the case of lignins with high levels of condensed units. Overall, these results indicate that mild hydrogenolysis could offer an alternative to thioacidolysis for probing lignin structure.


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