Process for rejuvenating used alkanolamaine solutions
AssigneeMobil Oil Corporation
InventorTsoung Y. Yan
Life of this patent
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Abstract
The present invention provides a method for rejuvenating an aqueous alkanolamine solution being at least partially deactivated from contact with an acid gas, said rejuvenation method comprising contacting said aqueous alkanolamine solution with hydrogen in the presence of a hydrotreating catalyst under hydrotreating conversion conditions including contact time sufficient to increase the acid gas sorption capacity of said aqueous alkanolamine solution.
Claims30
A method for increasing the AACI of an aqueous diethanolamine solution which has been at least partially deactivated from contact with an acid gas, said method comprising contacting said aqueous diethanolamine solution with hydrogen in the presence of a hydrotreating catalyst under conversion conditions of temperature from 30.degree. C. to 400.degree. C., liquid hourly space velocity from 0.01 hr.sup.-1 to 100 hr.sup.-1, pressure from 1 to 14,000 kPa, hydrogen dosage from 1 to 100 mols H.sub.2 per mol of diethanolamine, and contact time sufficient to convert diethanolamine degradation products to diethanolamine.
A method for increasing the AACI of an aqueous diethanolamine solution being at least partially deactivated from contact with an acid gas, said regeneration method comprising:
- (a) filtering said aqueous diethanolamine solution to remove suspended particulates;
- (b) contacting said filtered aqueous diethanolamine solution with an anionic ion-exchange resin;
- (c) contacting said aqueous diethanolamine solution with a cationic exchange resin;
- (d) reacting said aqueous diethanolamine solution with hydrogen in the presence of a hydrotreating catalyst under hydrotreating conversion conditions of temperature from 30.degree. C. to 400.degree. C., liquid hourly space velocity of from 0.1 hr.sup.-1 to 100 hr.sup.-1, pressure of from 1 to 14,000 kPa, hydrogen dosage from 1 to 100 mols H.sub.2 per mol of diethanolamine, and contact time sufficient to evolve a product stream having a higher concentration of diethanolamine that said at least partially deactivated diethanolamine solution.
A process for removing at least one of H.sub.2 S, CO.sub.2 and CO from a hydrocarbon gas stream containing the same comprising the steps of:
- (a) providing a hydrocarbon gas stream containing a recoverable concentration of H.sub.2 S, CO.sub.2 or CO;
- (b) contacting said hydrocarbon gas stream of step (a) with an aqueous alkanolamine solution containing alkanolamine to remove H.sub.2 S, CO.sub.2 or CO from said hydrocarbon gas stream, to convert at least a portion of said alkanolamine to degradation products having a lesser affinity for sorbing acid gases than said alkanolamine, and to evolve an alkanolamine solution enriched in H.sub.2 S, CO.sub.2 or CO;
- (c) stripping H.sub.2 S, CO.sub.2 or CO from said enriched alkanolamine solution of step (b) to evolve a lean alkanolamine solution containing both alkanolamine and said alkanolamine degradation products;
- (d) heating at least a portion of said lean aqueous alkanolamine stream of step (c) to elevated temperature and holding said lean aqueous alkanolamine solution of step (c) at said elevated temperature under hydrogen pressure in the presence of a hydrotreating catalyst for a period of time sufficient to rejuvenate said lean alkanolamine solution such that the rejuvenated lean alkanolamine solution exhibits increased acid gas sorption capacity per unit mass than stripped lean alkanolamine solution of step (c).
A method for increasing the acid gas sorption capacity of an aqueous alkanolamine solution which has been at least partially deactivated from contact with an acid gas, said method comprising contacting said aqueous alkanolamine solution with hydrogen in the presence of a hydrotreating catalyst under conversion conditions of temperature from 30.degree. C. to 400.degree. C., liquid hourly space velocity from 0.01 hr.sup.-1 to 100 hr.sup.-1, pressure from 1 to 14,000 kPa, hydrogen dosage from 1 to 100 mols H.sub.2 per mol of alkanolamine, and contact time sufficient to convert alkanolamine degradation products to alkanolamine.
Dependencies are inferred from the claim text.