TY - JOUR
T1 - Towards Improved Conversion of Wet Waste to Jet Fuel with Atomic Layer Deposition-Coated Hydrodeoxygenation Catalysts
T2 - Article No. 143268
AU - McNeary, W.
AU - Miller, Jacob
AU - Tacey, Sean
AU - Travis, Jonathan
AU - Lahti, Gabriella
AU - Griffin, Michael
AU - Jungjohann, Katherine
AU - Teeter, Glenn
AU - Eralp Erden, Tugce
AU - Farberow, Carrie
AU - Tuxworth, Luke
AU - Watson, Michael
AU - Dameron, Arrelaine
AU - Vardon, Derek
PY - 2023
Y1 - 2023
N2 - The conversion of wet waste-derived volatile fatty acids into jet fuel-range hydrocarbons is a promising route for increasing the production of sustainable aviation fuel; however, the cost and moderate alkane selectivity of Pt-based hydrodeoxygenation catalysts present challenges for commercialization. To address this, we used atomic layer deposition to apply TiO2 overcoats to Pt/Al2O3 catalysts and create new interface sites that exhibited 8 times higher site time yield of the desirable n-alkane product than uncoated catalyst. Through TPR/TPD, XPS, CO DRIFTS, and DFT calculations, we found that the increased selectivity of the ALD-coated catalyst was due to the creation of O vacancies at the Pt-TiO2 interface under reducing conditions, resulting in new Ti3+ acid sites near the active metal. Maximum conversion and alkane selectivity during HDO was achieved with an ALD-coated 0.5% wt Pt catalyst, indicating that TiO2 ALD can be used to maximize the utility of precious-metal catalysts.
AB - The conversion of wet waste-derived volatile fatty acids into jet fuel-range hydrocarbons is a promising route for increasing the production of sustainable aviation fuel; however, the cost and moderate alkane selectivity of Pt-based hydrodeoxygenation catalysts present challenges for commercialization. To address this, we used atomic layer deposition to apply TiO2 overcoats to Pt/Al2O3 catalysts and create new interface sites that exhibited 8 times higher site time yield of the desirable n-alkane product than uncoated catalyst. Through TPR/TPD, XPS, CO DRIFTS, and DFT calculations, we found that the increased selectivity of the ALD-coated catalyst was due to the creation of O vacancies at the Pt-TiO2 interface under reducing conditions, resulting in new Ti3+ acid sites near the active metal. Maximum conversion and alkane selectivity during HDO was achieved with an ALD-coated 0.5% wt Pt catalyst, indicating that TiO2 ALD can be used to maximize the utility of precious-metal catalysts.
KW - atomic layer deposition
KW - catalysis
KW - hydrodeoxygenation
KW - nanomaterials
KW - sustainable aviation fuel
UR - http://www.scopus.com/inward/record.url?scp=85159158356&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2023.143268
DO - 10.1016/j.cej.2023.143268
M3 - Article
SN - 1369-703X
VL - 467
JO - Biochemical Engineering Journal
JF - Biochemical Engineering Journal
ER -