In-situ catalytic upgrading of heavy oil using dispersed bionanoparticles supported on gram-positive and gram-negative bacteria

[Display omitted] •Heavy oil upgraded into lighter components via catalysts.•Commercial catalyst coking limits the reaction.•Bio-metallic Pd/Pt catalysts show reduced coking.•Bio-metallic Pd/Pt catalysts upgrade heavy oil better than commercial catalyst. With the continuous depletion of global oil r...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2017-04, Vol.203, p.807-819
Hauptverfasser: Omajali, Jacob B., Hart, Abarasi, Walker, Marc, Wood, Joseph, Macaskie, Lynne E.
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Hart, Abarasi
Walker, Marc
Wood, Joseph
Macaskie, Lynne E.
description [Display omitted] •Heavy oil upgraded into lighter components via catalysts.•Commercial catalyst coking limits the reaction.•Bio-metallic Pd/Pt catalysts show reduced coking.•Bio-metallic Pd/Pt catalysts upgrade heavy oil better than commercial catalyst. With the continuous depletion of global oil reserves, unconventional alternative oil resources like heavy oil and bitumen have become increasingly attractive. This study investigates the use of bimetallic bio-nanoparticles (bio-NPs), a potential alternative to commercial catalysts in heavy oil upgrading. The bio-NPs were made by sequential reduction of precious metal (Pd and Pt) ions with hydrogen as the electron donor at 5wt% and 20wt% metal loading using bacterial (Desulfovibrio desulfuricans and Bacillus benzeovorans) cells as support. The bio-NPs were characterized using transmission electron microscopy (TEM), X-ray powder diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). Results of the catalytic upgrading of a feed heavy oil show that the bimetallic bio-NPs produced an increment of ∼2° in API (American Petroleum Institute) gravity (i.e. ∼9.1°) better than monometallic bio-NPs (∼7.6°) on average while the API gravity using thermal upgrading was lower (6.3°). The API gravity of a commercial Ni-Mo/Al2O3 catalyst was 11.1°. However, more coking was produced using the commercial catalyst than with the bio-NPs. The extent of viscosity reduction was: 98.7% (thermal), 99.2% (bio-NPs) and 99.6% (Ni-Mo/Al2O3) below 1031mPas for the feed heavy oil reference (baseline). The potential advantage of using bio-NPs is that the precious metals can be sourced cheaply from waste streams, which could serve as a potential platform for the green synthesis of catalytically active materials using bacteria for in-situ catalytic upgrading of heavy oils.
doi_str_mv 10.1016/j.apcatb.2016.10.074
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With the continuous depletion of global oil reserves, unconventional alternative oil resources like heavy oil and bitumen have become increasingly attractive. This study investigates the use of bimetallic bio-nanoparticles (bio-NPs), a potential alternative to commercial catalysts in heavy oil upgrading. The bio-NPs were made by sequential reduction of precious metal (Pd and Pt) ions with hydrogen as the electron donor at 5wt% and 20wt% metal loading using bacterial (Desulfovibrio desulfuricans and Bacillus benzeovorans) cells as support. The bio-NPs were characterized using transmission electron microscopy (TEM), X-ray powder diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). Results of the catalytic upgrading of a feed heavy oil show that the bimetallic bio-NPs produced an increment of ∼2° in API (American Petroleum Institute) gravity (i.e. ∼9.1°) better than monometallic bio-NPs (∼7.6°) on average while the API gravity using thermal upgrading was lower (6.3°). 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subjects Aluminum oxide
Bacteria
Beryllium
Bimetals
Bio-nanoparticles
Catalysts
Chemical synthesis
Coke
Coking
Desulfovibrio desulfuricans
Diffraction
Electron microscopy
Gram-negative bacteria
Gravitation
Heavy oil
Metals
Molybdenum
Nanoparticles
Noble metals
Oil
Palladium
Photoelectron spectroscopy
Platinum
Powder
Reduction (metal working)
Spectroscopy
Transmission electron microscopy
Upgrading
Viscosity
Waste management
Waste streams
X ray photoelectron spectroscopy
X-ray diffraction
title In-situ catalytic upgrading of heavy oil using dispersed bionanoparticles supported on gram-positive and gram-negative bacteria
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