High surface area graphene-supported metal chalcogenide assembly
US-2016145504-A1 · May 26, 2016 · US
US9233359B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9233359-B2 |
| Application number | US-201113808425-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 5, 2011 |
| Priority date | Jul 6, 2010 |
| Publication date | Jan 12, 2016 |
| Grant date | Jan 12, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention concerns a process for upgrading lower quality carbonaceous feedstock using a slurry catalyst composition. The use of particular organometallic compounds as precursors for the dispersed active catalyst allows for reduced coke formation.
Opening claim text (preview).
The invention claimed is: 1. A process for the hydroconversion of a lower quality hydrocarbonaceous feedstock, wherein the process comprises: converting a precursor composition into an active slurry catalytic phase, and hydroconverting the lower quality hydrocarbonaceous feedstock using the active slurry catalytic phase; and wherein the precursor composition comprises at least one organometallic coordination compound of formula C 1 C 2 ML n (I), where M is a transition metal selected from group IIA, IIIB, IVB, VB, VIB, VIIB, VIII, IB or IIB of the periodic table of elements, and wherein M is not Fe, —C 1 and —C 2 are monocyclic or polycyclic aryl hydrocarbon ligands that are pi-bonded to M, —C 1 and —C 2 being the same or different, each of —C 1 or —C 2 comprising from 0 to 5 substituents R, each substituent R being the same or different, R being selected from: a C3-C8 substituted or unsubstituted, monocyclic or polycyclic ring structure that is partially unsaturated, unsaturated or aromatic, fused or not fused to the ligand —C1 or —C2, a C3-C8 substituted or unsubstituted, partially unsaturated or unsaturated, linear or branched, alicyclic hydrocarbyl radical, a C1-C8, substituted or unsubstituted, linear or branched, saturated hydrocarbyl radical, —C 1 and —C 2 being independent or connected via at least one substituent R, -L is a ligand that is sigma-bonded to M, n is an integer equal to 0 to 3, each -L is, independently, a univalent ligand. 2. The process according to claim 1 , wherein each of C 1 or C 2 is a C5-C8 monocyclic polyene ligand comprising from 0 to 5 substituents R, each substituent R being the same of different, R being defined as in claim 1 . 3. The process according to claim 1 , wherein each of C 1 and C 2 is a cyclopentadienyl ligand comprising from 0 to 5 substituents R, each substituent R being the same or different, R being defined as in claim 1 . 4. The process according to claim 1 , wherein the organometallic coordination compound is a metallocene compound presenting the general formula (II) below wherein the R substituted or unsubstituted cyclopentadienyl ligands are pi-bonded to M, and L ligands are sigma-bonded to M, and where M, L, R and n are defined as in formula (I). 5. The process according to claim 1 , wherein -L is selected from Hydride (-L=—H), Halide (-L=—F, —Cl, —Br, —I), cyanide (-L=—CN), Alkoxide (-L=—OR), Thiolate (-L=—SR), Amide (-L=—NR2), Phosphide (-L=—PR2), Alkyl (-L=—CH2R or other), Alkenyl (-L=—CHCHR), Alkynyl (-L=—CCR), Acyl (-L=—COR), Isocyanide (-L=—CNR), Nitrosyl (-L=—NO), Diazenide (-L=—NNR), Imide (-L=═NR), L=-ER3 or -EX3 (with E=Si, Ge, Sn), -L=—PR3, —PX3, —AsR3, —SbR3, amines, L=ER2 (with E=O, S, Se, Te), where X is an halogen atom, R is a C1-C8, preferably a C1-C6, linear or branched, alkyl, alkenyl Group or a C3-C8 alicyclic or aromatic group. 6. The process according to claim 1 , wherein M is selected from Group IIA, IIB, IIIB, IVB, VB, VIB, VIIB or VIII of the periodic table of the elements, and wherein M is not Fe. 7. The process according to claim 1 , wherein M is V or Mo. 8. The process according to claim 1 , wherein said precursor composition furthermore comprises at least one surfactant and/or a least one promoter. 9. The process according to claim 1 , wherein said precursor composition furthermore comprises a solvent. 10. The process according to claim 9 , wherein the solvent is a hydrocarbonaceous compound. 11. The process according to claim 1 , comprising a step of sulfiding said precursor composition using a sulfiding agent. 12. The process according to claim 11 , wherein said sulfiding step is performed before introduction of said precursor in the feedstock or after introduction of said precursor in the feedstock. 13. The process according to claim 1 , wherein the lower quality hydrocarbonaceous feedstock an atomic H/C ratio of at least 0.25. 14. The process according to claim 1 , wherein the lower quality hydrocarbonaceous feedstock is selected from atmospheric and vacuum residues, pitch coming from deasphalting, deasphalted oil, visbroken effluents, shale oils, biomass ex-pyrolysis, biomass ex-hydrothermal treatment, coal, petcoke from delayed coker, tires, polymers, road bitumen.
Activation · CPC title
with iron group metals or platinum group metals · CPC title
Atmospheric residues having a boiling point of at least about 538 °C · CPC title
Vanadium · CPC title
suspended in the oil, e.g. slurries · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.