Hydrocarbon-soluble molybdenum catalyst precursors and methods for making same
View Patent ↗Hydrocarbon-soluble molybdenum catalyst precursors include a plurality of molybdenum cations that are each bonded with a plurality of organic anions to form an oil soluble molybdenum salt. A portion of the molybdenum atoms are in the 3+ oxidation state such that the plurality of molybdenum atoms has an average oxidation state of less than 4+, e.g., less than about 3.8+, especially less than about 3.5+. The catalyst precursors can form a hydroprocessing molybdenum sulfide catalyst in heavy oil feedstocks. The oil soluble molybdenum salts are manufactured in the presence of a reducing agent, such as hydrogen gas, to obtain the molybdenum in the desired oxidation state. Preferably the reaction is performed with hydrogen or an organic reducing agent and at a temperature such that the molybdenum atoms are reduced to eliminate substantially all molybdenum oxide species.
1. A method of making a molybdenum catalyst precursor for hydrocracking heavy oil, comprising:
providing a plurality of molybdenum atoms;
providing an organic agent comprising a plurality of organic molecules having at least one functional group that is reactive with the molybdenum atoms; and
reacting the plurality of molybdenum atoms with the organic agent in the presence of a reducing agent and in a molar ratio of molybdenum atoms to organic molecules of less than 1:4 to yield the molybdenum catalyst precursor comprised of a molybdenum salt having a plurality of molybdenum atoms with an average oxidation state of less than 4+.
2. A method as in claim 1 , wherein the reducing agent comprises hydrogen or an organic reducing agent or both.
3. A method as in claim 1 , wherein the plurality of organic anions comprises anions having between 2 and 14 carbon atoms.
4. A method as in claim 1 , wherein the organic anion is a carboxylate anion.
5. A molybdenum catalyst precursor as in claim 4 , wherein the carboxylate anions are selected from the group consisting of butanoic acid, pentanoic acid, hexanoic acid, heptanoic acid, octanoic acid, decanoic acid, 2-ethyl butanoic acid, 2-methyl pentanoic acid, 2-ethyl hexanoic acid, and combinations thereof.
6. A method as in claim 1 , wherein the weight percent molybdenum in the molybdenum catalyst precursor is greater than about 15.5%.
7. A method as in claim 1 , wherein the percent of molybdenum in the molybdenum catalyst precursor is greater than about 17%.
8. A method as in claim 1 , further comprising reacting one or more additional metal salts comprising a transition metal other than molybdenum with the organic agent.
9. A method as in claim 1 , further comprising forming a diluted molybdenum catalyst precursor by mixing the molybdenum catalyst precursor with a diluent.
10. A method as in claim 9 , further comprising forming a blended heavy oil feedstock by mixing the diluted molybdenum catalyst precursor with a heavy oil feedstock.
11. A method as in claim 1 , further comprising forming a blended heavy oil feedstock by mixing the molybdenum catalyst precursor with a heavy oil feedstock.
12. A method as in claim 1 , wherein the reducing agent comprises hydrogen and optionally an organic reducing agent selected from the group consisting of methane, ethane, olefins, ethylene, propylene, aldehydes and formaldehyde.
13. A method as in claim 1 , wherein the reaction between the plurality of molybdenum atoms and organic agent in the presence of the reducing agent is carried out at a temperature above about 100° C. such that water in the reaction product is removed as the reaction product is formed.
14. A method as in claim 1 , wherein the reaction between the plurality of molybdenum atoms and organic agent in the presence of the reducing agent is performed at a temperature greater than 155° C.
15. A method as in claim 1 , wherein the reaction mixture is purged with an inert gas prior to reducing with the reducing agent.
16. A method as in claim 1 , wherein the average oxidation state of the molybdenum atoms of the molybdenum catalyst precursor is less than about 3.8+.
17. A method as in claim 1 , wherein the average oxidation state of the molybdenum atoms of the molybdenum catalyst precursor is less than about 3.5+.
18. A method as in claim 1 , wherein the molybdenum catalyst precursor forms a molybdenum salt having fewer complexed molecules that inhibit the molybdenum salt from forming a molybdenum sulfide compound than catalyst precursors manufactured without the use of the reducing agent.
19. A method of making a molybdenum catalyst precursor suitable for hydrocracking heavy oil, comprising:
providing a plurality of molybdenum atoms;
providing an organic agent comprising a plurality of organic molecules having at least one functional group that is reactive with the molybdenum atoms;
reacting the plurality of molybdenum atoms with the organic agent in the presence of hydrogen and/or an organic reducing agent selected from the group consisting of methane, ethane, olefins, ethylene, propylene, aldehydes and formaldehyde at a temperature greater than about 90° C. to form a reaction product comprising a hydrocarbon-soluble molybdenum salt including a plurality of molybdenum atoms with an average oxidation state of less than 3.8+.
20. A method as in claim 19 , wherein the organic agent molecules are selected from the group consisting of butanoic acid, pentanoic acid, hexanoic acid, heptanoic acid, octanoic acid, decanoic acid, 2-ethyl butanoic acid, 2-methyl pentanoic acid, 2-ethyl hexanoic acid, and combinations thereof.
21. A method as in claim 19 , wherein the molybdenum atoms are reacted with the organic agent in the presence of the hydrogen and/or the organic reducing agent at a temperature greater than about 100° C.
22. A method as in claim 19 , wherein the molybdenum atoms are reacted with the organic agent in the presence of the hydrogen and/or the organic reducing agent at a temperature greater than 155° C.
23. A method as in claim 19 , wherein the molybdenum catalyst precursor forms a molybdenum salt having higher solubility than a catalyst precursor prepared without the presence of hydrogen.
24. A method of making a molybdenum catalyst precursor for hydrocracking heavy oil, comprising:
providing a plurality of molybdenum atoms;
providing an organic agent comprising a plurality of organic molecules having at least one functional group that is reactive with the molybdenum atoms; and
reacting the plurality of molybdenum atoms with the organic agent in the presence of hydrogen at a temperature greater than about 100° C. and in a molar ratio of molybdenum atoms to organic molecules of less than about 1:3.5 to yield the molybdenum catalyst precursor comprised of a molybdenum salt having a plurality of molybdenum atoms with an average oxidation state of less than about 3.5.
25. A method as in claim 1 , wherein the molar ratio of molybdenum atoms to organic molecules is less than about 1:3.5.