초록 ▼

The invention relates to a method for treating and upgrading a hydrocarbon containing acidic species such as mercaptans, comprising: (a) contacting the hydrocarbon, in the essential absence of oxygen, with a first phase of a treatment composition containing water, dissolved alkali metal hydroxide, c

The invention relates to a method for treating and upgrading a hydrocarbon containing acidic species such as mercaptans, comprising: (a) contacting the hydrocarbon, in the essential absence of oxygen, with a first phase of a treatment composition containing water, dissolved alkali metal hydroxide, cobalt phthalocyanine sulfonate, and dissolved alkylphenylates and having at least two phases, (i) the first phase containing water, alkali metal alkylphenylate, dissolved alkali metal hydroxide, and dissolved sulfonated cobalt phthalocyanine, and (ii) the second phase containing water and dissolved alkali metal hydroxide; and then (b) separating an upgraded hydrocarbon.

대표청구항 ▼

What is claimed is: 1. A method for upgrading a hydrocarbon containing mercaptans, comprising: (a) contacting the hydrocarbon under substantially anaerobic conditions with a first phase of a treatment composition containing water, alkali metal hydroxide, cobalt phthalocyanine sulfonate, and alkylph

What is claimed is: 1. A method for upgrading a hydrocarbon containing mercaptans, comprising: (a) contacting the hydrocarbon under substantially anaerobic conditions with a first phase of a treatment composition containing water, alkali metal hydroxide, cobalt phthalocyanine sulfonate, and alkylphenols and having at least two phases, (i) the first phase containing dissolved alkali metal alkylphenylate, dissolved alkali metal hydroxide, water, and dissolved sulfonated cobalt phthalocyanine, and (ii) the second phase containing water and dissolved alkali metal hydroxide; (b) extracting mercaptan sulfur from the hydrocarbon to the first phase; (c) separating an upgraded hydrocarbon; (d) conducting an oxidizing amount oxygen and the first phase containing mercaptan sulfur to an oxidizing region and oxidizing the mercaptan sulfur to disulfides; (e) separating the disulfides from the first phase; and then (f) conducting the first phase to step (a) for re-use. 2. The method of claim 1 wherein, during the contacting of step (a), the first phase is applied to and flows over and along hydrophylic metal fibers, and the hydrocarbon flows over the first phase co-current with first phase flow. 3. The method of claim 2 wherein the hydrocarbon contains a hydrotreated naphtha and at least a portion of the mercaptans are reversion mercaptans. 4. The method of claim 3 wherein the hydrotreated naphtha is a selectively hydrotreated naphtha and wherein the reversion mercaptans have a molecular weight greater than about C4. 5. The method of claim 3 wherein the reversion mercaptans have a molecular weight greater than about C5. 6. The method of claim 1 wherein the sulfonated cobalt phthalocyanine is present in the first phase in an amount ranging from about 10 to about 500 wppm, based upon the weight of the treatment solution. 7. The method of claim 1 wherein the treatment composition contains about 15 wt. % to about 55 wt. % dissolved alkylphenols, about 10 wppm to about 500 wppm dissolved sulfonated cobalt phthalocyanine, about 25 wt. % to about 60 wt. % dissolved alkali metal hydroxide, and about 10 wt. % to about 50 wt. % water, based on the weight of the treatment solution. 8. The method of claim 7 wherein the first phase is present in step (a) in an amount ranging from about 3 vol. % to about 100 vol. %, based on the volume of the hydrocarbon, and the contacting is conducted in the substantial absence of oxygen. 9. The method of claim 1 wherein at least a portion of the alkylphenols are cresols obtained from the hydrocarbon. 10. The method of claim 1 wherein the sulfonated cobalt phthalocyanine is cobalt phthalocyanine disulfonate. 11. The method of claim 1 further comprising conducting at least a portion of the first phase in step (f) to a polishing region wherein a water-immiscible solvent further separates disulfides from the first phase prior to the re-use of the first phase. 12. The method of claim 11 further comprising (g) conducting the first phase from the oxidizing region or the polishing region to the second phase of step (a); (h) conducting the second phase of step (a) to a concentrating region and removing water from the second phase; and (i) conducting the second phase from the concentrating region to step (a). 13. The method of claim 12 wherein the treatment composition is formed by combining water in an amount ranging from about 10 wt. % to about 50 wt. %, alkali metal hydroxide in an amount ranging from about 25 wt. % to about 60 wt. %, sulfonated cobalt phthalocyanine in an amount ranging from about 10 wppm to about 500 wppm, and alkylphenols in an amount ranging from about 10 wt. % to about 50 wt. %, based on the weight of the treatment solution. 14. The method of claim 13 wherein (i) the hydrocarbon is a selectively hydrotreated naphtha containing reversion mercaptans, (ii) at least a portion of the alkylphenols are cresols obtained from the selectively hydrotreated naphtha, (iii) wherein the reversion mercaptans have a molecular weight greater than about C5, and (iv) the sulfonated cobalt pthalocyanine is cobalt pthalocyanine disulfonate. 15. A method for treating and upgrading a hydrocarbon containing mercaptans, comprising: (a) contacting the hydrocarbon under substantially anaerobic conditions with an extractant composition containing water, alkali metal hydroxide, cobalt phthalocyanine sulfonate, and alkylphenols, wherein (i) the extractant is substantially immiscible with its analogous aqueous alkali metal hydroxide, and (ii) the extractant contains water, alkali metal alkylphenylate, alkali metal hydroxide, and sulfonated cobalt phthalocyanine; (b) extracting mercaptan sulfur from the hydrocarbon to the extractant; (c) separating an upgraded hydrocarbon; (d) conducting an oxidizing amount oxygen and the extractant containing mercaptan sulfur to an oxidizing region and oxidizing the mercaptan sulfur to disulfides; (e) separating the disulfides from the extractant; and then (f) conducting the extractant to step (a) for re-use. 16. The method of claim 15 wherein the hydrocarbon contains a hydrotreated naphtha and at least a portion of the mercaptans are reversion mercaptans having a molecular weight greater than about C 4. 17. The method of claim 16 wherein the hydrotreated naphtha is a selectively hydrotreated naphtha and wherein the reversion mercaptans have a molecular weight greater than about C5. 18. The method of claim 15 wherein, during the contacting of step (a), the first phase is applied to and flows over and along hydrophylic metal fibers, and the hydrocarbon flows over the first phase co-current with first phase flow. 19. The method of claim 15 wherein the treatment composition is formed by combining water in an amount ranging from about 10 wt. % to about 50 wt. %, alkali metal hydroxide in an amount ranging from about 25 wt. % to about 60 wt. %, sulfonated cobalt phthalocyanine in an amount ranging from about 10 ppm to about 500 ppm, and alkylphenols in an amount ranging from about 10 wt. % to about 50 wt. %, based on the weight of the treatment solution, and wherein at least a portion of the alkyl phenols are cresols obtained from the hydrocarbon. 20. The method of claim 19 wherein the extractant is present in an amount ranging from about 3 vol. % to about 100 vol. %, based on the volume of the hydrocarbon, and wherein the extractant contains dissolved alkali metal hydroxide in an amount ranging from about 1 wt. % to about 40 wt. %, dissolved alkali metal alkylphenylate ions in an amount ranging from about 10 wt. % to about 95 wt. %, and sulfonated cobalt pthalocyanine in an amount ranging from about 10 ppm to about 500 ppm, based on the weight of the extractant. 21. The method of claim 20 wherein the sulfonated cobalt phthalocyanine is cobalt phthalocyanine disulfonate. 22. The method of claim 15 further comprising conducting at least a portion of the extractant in step (f) to a polishing region wherein a water-immiscible solvent further separates disulfides from the extractant prior to the re-use of the extractant. 23. The method of claim 22 further comprising (g) conducting the first phase from the oxidizing region or the polishing region to the second phase of step (a); (h) conducting the second phase of step (a) to a concentrating region and removing water from the second phase; and (i) conducting the second phase from the concentrating region to step (a). 24. The method of claim 23 wherein (i) the hydrocarbon is a selectively hydrotreated naphtha containing reversion mercaptans, (ii) at least a portion of the alkylphenols are cresols obtained from the selectively hydrotreated naphtha, (iii) wherein the reversion mercaptans have a molecular weight greater than about C5, and (iv) the sulfonated cobalt pthalocyanine is cobalt pthalocyanine disulfonate.