Abstract
Inexpensive Ni-based catalysts can afford comparable performance to costly precious metal formulations in the conversion of fat, oil, or greases (FOG) to fuel-like hydrocarbons via decarboxylation/decarbonylation (deCOx). While the addition of certain metals has been observed to promote Ni-based deCOx catalysts, the steady-state performance of bimetallic formulations must be ascertained using industrially relevant feeds and reaction conditions in order to make meaningful comparisons. In the present work, used cooking oil (UCO) was upgraded to renewable diesel via deCOx over Ni/Al2O3 promoted with Cu, Fe, or Pt in a fixed-bed reactor at 375◦C using a weight hourly space velocity (WHSV) of 1 h−1. Although all catalysts fully deoxygenated the feed to hydrocarbons throughout the entire 76 h duration of these experiments, the cracking activity (and the evolution thereof) was distinct for each formulation. Indeed, that of the Ni-Cu catalyst was low and relatively stable, that of the Ni-Fe formulation was initially high but progressively dropped to become negligible, and that of the Ni-Pt catalyst started as moderate, varied considerably, and finished high. Analysis of the spent catalysts suggests that the evolution of the cracking activity can be mainly ascribed to changes in the composition of the metal particles.
Original language | English |
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Article number | 91 |
Journal | Catalysts |
Volume | 10 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2020 |
Bibliographical note
Publisher Copyright:© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
Funding
Funding: This work was supported in part by the National Science Foundation (grant No. 1437604); by the J. William Fulbright Foreign Scholarship Board and the Bureau of Educational and Cultural Affairs of the United States Department of State through a Fulbright Scholarship awarded to G.S; and by the French National Center for Scientific Research (CNRS) Graduate School EIPHI (contract ANR-17-EURE-0002) and through a CNRS visiting researcher position granted to E.S.-J. This work was supported in part by the National Science Foundation (grant No. 1437604); by the J. William Fulbright Foreign Scholarship Board and the Bureau of Educational and Cultural Affairs of the United States Department of State through a Fulbright Scholarship awarded to G.S; and by the French National Center for Scientific Research (CNRS) Graduate School EIPHI (contract ANR-17-EURE-0002) and through a CNRS visiting researcher position granted to E.S.-J. Sarah Cummins and the Redwood Cooperative School in Lexington, Kentucky, as well as Jennifer Wyatt and personnel from the Lexington-Fayette Urban Country Government, are thanked for collecting and delivering the used cooking oil used in this study. Tonya Morgan is thanked for her help with the GC-MS analysis of liquid reaction products.
Funders | Funder number |
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Bureau of Educational and Cultural Affairs of the United States Department of State | |
EIPHI-BFC | ANR-17-EURE-0002 |
French National Center for Scientific Research | |
J. William Fulbright Foreign Scholarship Board | |
National Science Foundation (NSF) | 1437604 |
U.S. Department of State Bureau of Educational and Cultural Affairs | |
CNRS Centre National de la Recherche Scientifique |
Keywords
- Copper
- Decarbonylation
- Decarboxylation
- Deoxygenation
- Hydrocarbons
- Iron
- Nickel
- Platinum
- Used cooking oil
ASJC Scopus subject areas
- Catalysis
- Physical and Theoretical Chemistry