Azizova, Liana R.

Balu, Alina M.

Ilchenko, Mykola M.

Kartel, Mykola T.

Kulik, Tetiana V.

Luque, Rafael

Palianytsia, Borys B.

Roldan, Alberto

Tarnavskiy, Sergiy

Telbiz, German  M.

Fatty acids (FA) are the main constituents of lipids and oil crop waste, considered to be a promising 2G biomass that can be converted into ketenes via catalytic pyrolysis. Ketenes are appraised as promising synthons for the pharmaceutical, polymer, and chemical industries. Progress in the thermal conversion of short- and long-chain fatty acids into ketenes requires a deep understanding of their interaction mechanisms with the nanoscale oxide catalysts. In this work, the interactions of fatty acids with silica are investigated using a wide range of experimental and computational techniques (TPD MS, DFT, FTIR, in situ IR, equilibrium adsorption, and thermogravimetry). The adsorption isotherms of linear and branched fatty acids C1–C6 on the silica surface from aqueous solution have been obtained. The relative quantities of different types of surface complexes, as well as kinetic parameters of their decomposition, were calculated. The formation of surface complexes with a coordination bond between the carbonyl oxygens and silicon atoms in the surface-active center, which becomes pentacoordinate, was confirmed by DFT calculations, in good agreement with the IR feature at ∼1680 cm 1. Interestingly, ketenes release relate to these complexes’ decomposition as confirmed by the thermal evolution of the absorption band (1680 cm–1) synchronously with the TPD peak of the ketene molecular ion. The established regularities of the ketenezation are also observed for the silica-induced pyrolysis of glyceryl trimyristate and real waste, rapeseed meals

Online Research @ Cardiff

The role of surface complexes in ketenes formation from fatty acids via pyrolysis over silica: from platform molecules to waste biomass

The role of surface complexes in ketenes formation from fatty acids via pyrolysis over silica: from platform molecules to waste biomass

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