Composition of additives comprising a copolymer and a resin
US-2024076567-A1 · Mar 7, 2024 · US
US9845437B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9845437-B2 |
| Application number | US-201615040778-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 10, 2016 |
| Priority date | Feb 12, 2015 |
| Publication date | Dec 19, 2017 |
| Grant date | Dec 19, 2017 |
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A method of passivating a metal surface of hydrocarbon processing equipment is provided in which a water soluble molybdate compound is introduced into water or steam which is in contact or will come into contact with a metal surface of the hydrocarbon processing equipment to passivate the metal surface to inhibit surface coke formation.
Opening claim text (preview).
What is claimed is: 1. A method of passivating a metal surface of hydrocarbon processing equipment, the method comprising: removing coke from a metal surface of hydrocarbon processing equipment during a decoking process while the hydrocarbon processing equipment is shut down; and introducing a water soluble molybdate compound into water or steam which is in contact or will come into contact with the metal surface of the hydrocarbon processing equipment to passivate the metal surface while the hydrocarbon processing equipment is shut down, wherein the temperature in the hydrocarbon processing equipment ranges from about 15° C. to about 650° C. during passivation. 2. The method of claim 1 , wherein the molybdate compound comprises an alkali metal molybdate, an alkaline earth metal molybdate, ammonium molybdate, molybdic acid, or cerous molybdate. 3. The method of claim 2 , wherein the alkali metal molybdate comprises sodium molybdate or potassium molybdate. 4. The method of claim 3 wherein the alkali metal molybdate comprises sodium molybdate. 5. The method of claim 2 , wherein the alkaline earth metal molybdate comprises magnesium molybdate. 6. The method of claim 1 , wherein the molybdate compound is added to the water or steam in a concentration of about 10 to about 25,000 ppm. 7. The method of claim 1 , wherein the molybdate compound is introduced during or after an online spalling, mechanical pigging, or steam/air burning process. 8. The method of claim 7 , wherein the molybdate compound is introduced during an online spalling process. 9. The method of claim 7 , wherein the molybdate compound is introduced during a mechanical pigging process. 10. The method of claim 7 , wherein the molybdate compound is introduced during a steam/air burning process. 11. The method of claim 7 , wherein the molybdate compound is introduced after an online spalling process. 12. The method of claim 7 , wherein the molybdate compound is introduced after a mechanical pigging process. 13. The method of claim 7 , wherein the molybdate compound is introduced after a steam/air burning process. 14. The method of claim 1 , wherein the hydrocarbon processing equipment is a pass of a furnace, and the molybdate compound is added and the passivation occurs without shutting down other passes of the furnace or the hydrocarbon processing equipment is part of a refinery or petrochemical plant. 15. The method of claim 1 , wherein the hydrocarbon processing equipment comprises a thermal conversion unit, a heat exchanger, a visbreaker, a coker, a fired heater, a fractionator, a tube, a pipe, a tank, or a reactor. 16. The method of claim 1 , wherein the molybdate compound is introduced into a water tank connected to a feed inlet of the hydrocarbon processing equipment, or the molybdate compound is introduced into a water or steam inlet of the hydrocarbon processing equipment. 17. The method of claim 1 , wherein corrosion or fouling of the metal surface is inhibited as compared to the same metal surface under the same conditions without the passivation. 18. The method of claim 1 , wherein induction time before coking occurs on the metal surface of the hydrocarbon processing equipment is increased as compared to the same metal surface under the same conditions without the passivation. 19. The method of claim 1 , wherein the passivation is about the same or better than the passivation obtained using a phosphate ester for passivation at the same temperature for the same length of time.
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