TY - JOUR
T1 - Effect of Pt promotion on the Ni-catalyzed deoxygenation of tristearin to fuel-like hydrocarbons
AU - Loe, Ryan
AU - Huff, Kelsey
AU - Walli, Morgan
AU - Morgan, Tonya
AU - Qian, Dali
AU - Pace, Robert
AU - Song, Yang
AU - Isaacs, Mark
AU - Santillan-Jimenez, Eduardo
AU - Crocker, Mark
N1 - Publisher Copyright:
© 2019 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2019/2
Y1 - 2019/2
N2 - Pt represents an effective promoter of supported Ni catalysts in the transformation of tristearin to green diesel via decarbonylation/decarboxylation (deCOx), conversion increasing from 2% over 20% Ni/Al2O3 to 100% over 20% Ni-0.5% Pt/Al2O3 at 260◦C. Catalyst characterization reveals that the superior activity of Ni-Pt relative to Ni-only catalysts is not a result of Ni particle size effects or surface area differences, but rather stems from several other phenomena, including the improved reducibility of NiO when Pt is present. Indeed, the addition of a small amount of Pt to the supported Ni catalyst dramatically increases the amount of reduced surface metal sites, which are believed to be the active sites for deCOx reactions. Further, Pt addition curbs the adsorption of CO on the catalyst surface, which decreases catalyst poisoning by any CO evolved via decarbonylation, making additional active sites available for deoxygenation reactions and/or preventing catalyst coking. Specifically, Pt addition weakens the Ni-CO bond, lowering the binding strength of CO on surface Ni sites. Finally, analysis of the spent catalysts recovered from deCOx experiments confirms that the beneficial effect of Pt on catalyst performance can be partially explained by decreased coking and fouling.
AB - Pt represents an effective promoter of supported Ni catalysts in the transformation of tristearin to green diesel via decarbonylation/decarboxylation (deCOx), conversion increasing from 2% over 20% Ni/Al2O3 to 100% over 20% Ni-0.5% Pt/Al2O3 at 260◦C. Catalyst characterization reveals that the superior activity of Ni-Pt relative to Ni-only catalysts is not a result of Ni particle size effects or surface area differences, but rather stems from several other phenomena, including the improved reducibility of NiO when Pt is present. Indeed, the addition of a small amount of Pt to the supported Ni catalyst dramatically increases the amount of reduced surface metal sites, which are believed to be the active sites for deCOx reactions. Further, Pt addition curbs the adsorption of CO on the catalyst surface, which decreases catalyst poisoning by any CO evolved via decarbonylation, making additional active sites available for deoxygenation reactions and/or preventing catalyst coking. Specifically, Pt addition weakens the Ni-CO bond, lowering the binding strength of CO on surface Ni sites. Finally, analysis of the spent catalysts recovered from deCOx experiments confirms that the beneficial effect of Pt on catalyst performance can be partially explained by decreased coking and fouling.
KW - Decarbonylation
KW - Decarboxylation
KW - Deoxygenation
KW - Hydrocarbons
KW - Nickel
KW - Platinum
KW - Triglycerides
KW - Tristearin
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U2 - 10.3390/catal9020200
DO - 10.3390/catal9020200
M3 - Article
AN - SCOPUS:85063452310
SN - 2073-4344
VL - 9
JO - Catalysts
JF - Catalysts
IS - 2
M1 - 200
ER -