Methods for desalinating aqueous compositions through hetero-azeotropic distillation

US10874957B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10874957-B2
Application numberUS-201916255034-A
CountryUS
Kind codeB2
Filing dateJan 23, 2019
Priority dateJan 23, 2019
Publication dateDec 29, 2020
Grant dateDec 29, 2020

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  5. First independent claim

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Abstract

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A method of desalinating an aqueous composition includes forming a hetero-azeotrope mixture by combining the aqueous composition with an entrainer, the aqueous composition including at least one salt, and subjecting the hetero-azeotrope mixture to distillation at a distillation temperature of less than the boiling temperature of the aqueous composition for an operating distillation pressure, resulting in separating the hetero-azeotrope mixture into a distillation bottoms liquid and a multi-phase condensate. The method includes recovering the multi-phase condensate having an entrainer-rich phase and an aqueous phase, the aqueous phase comprising desalinated water, and removing a portion of the aqueous phase from the multi-phase condensate to recover the desalinated water. Systems for conducting the method of desalinating an aqueous stream are also disclosed.

First claim

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What is claimed is: 1. A method for desalinating an aqueous composition, the method comprising: forming a hetero-azeotrope mixture by combining at least a portion of the aqueous composition with at least one entrainer, the at least a portion of the aqueous composition comprising at least one salt, where the aqueous composition is selected from the group consisting of seawater, salty wastewater, produced water from hydrocarbon drilling, production or refining operations, and combinations of these; subjecting the hetero-azeotrope mixture to distillation at a distillation temperature of less than a boiling temperature of the aqueous composition at an operating distillation pressure, which results in separation of the hetero-azeotrope mixture into a distillation bottoms liquid and a multi-phase condensate; recovering the multi-phase condensate, the multi-phase condensate comprising an entrainer-rich phase and an aqueous phase, the aqueous phase comprising desalinated water; and removing at least a portion of the aqueous phase from the multi-phase condensate to recover the desalinated water. 2. The method of claim 1 , in which the aqueous composition is briny water having a salinity of from 3 grams per liter (g/L) to 300 g/L. 3. The method of claim 1 , further comprising: separating at least a portion of the entrainer-rich phase from the multi-phase condensate; and passing the at least a portion of the entrainer-rich phase back to the hetero-azeotrope mixture. 4. The method of claim 1 , in which the hetero-azeotrope mixture comprises from 20 volume percent (vol. %) to 95 vol. % aqueous composition based on a total volume of the hetero-azeotrope mixture. 5. The method of claim 1 , in which the hetero-azeotrope mixture has a hetero-azeotrope boiling temperature of less than 100° C. at the operating distillation pressure. 6. The method of claim 1 , in which the at least one entrainer is chemically stable and the at least one entrainer does not react with water, at least one salt, or organic compounds in the aqueous composition. 7. The method of claim 1 , in which the at least one entrainer has a solubility in water of less than 20 grams per 100 grams of water at 25° C. and atmospheric pressure. 8. The method of claim 1 , in which the entrainer is selected from the group consisting of an alkane, an alkene, an aromatic, an ester, an alcohol, a thiol, a disulfide, a sulfide, an ether, a ketone, a nitro group, and combinations of these. 9. The method of claim 1 , in which the entrainer is selected from 2-methyl-1,3-butadiene; pentane; 2-methyl-2-butene; methylenecyclobutane; carbon disulfide; 1-hexene; ethyl formate; 4-methyl-2-pentene; 3-methyl-3-buten-1-ol; hexane; isopropyl ether; cis-1-butenyl ethyl ether; 1-butenyl methyl ether; benzene; cyclohexane; ethyl acetate; cyclohexene; methyl propanoate; propyl formate; isopropyl acetate; ethylbutyl ether; isopropylacetate; butyl ethyl ether; 1-heptene; 2,5-dimethylfuran; 2,2,4-trimethylpentane; heptane; isobutyl formate; methylisopropenyl ketone; diisobutylene; propyl acetate; 3-pentanone; allyl acetate; nitroethane; 2,6-dimethyl-4-heptanol; toluene; 1,2-propanediol diacetate; butyl isopropenyl ether; 2-methyl-2-butanol; methylisobutyl ketone; isobutyl acetate; 2-methylpropyl acetate; cyclopropyl methyl ketone; propyl propanoate; octane; isobutyl alcohol; 2-pentanol, or combinations of these entrainers. 10. The method of claim 1 , where forming the hetero-azeotrope mixture comprises combining the aqueous composition with a plurality of entrainers. 11. The method of claim 1 , in which the distillation comprises short path distillation conducted in a distillation unit comprising a distillation vessel and a short-path distillation column fluidly coupled to the distillation vessel, in which a short path ratio (H L /H T ) of the distillation unit is from 0.2 to 0.5, where the short path ratio is defined as a height (H L ) of a vapor-liquid interface from a bottom of a distillation vessel to a total height (H T ), which includes a distance from the bottom of the distillation vessel to a top of a short path distillation column coupled to the distillation vessel. 12. The method of claim 1 , in which subjecting the hetero-azeotrope mixture to distillation is conducted in a distillation vessel having an aspect ratio (L/H V ) of from 2 to 5, in which the aspect ratio of the distillation vessel is defined as a length (L) of the distillation vessel divided by a height (H V ) of the distillation vessel. 13. The method of claim 1 , further comprising subjecting at least a portion of the distillation bottoms liquid to crystallization which results in separation of the distillation bottoms liquid into a salt product and a brine composition. 14. The method of claim 1 , in which the aqueous composition has salinity greater than 200 grams per liter (g/L) and the method further comprises: reducing the salinity of the hetero-azeotrope mixture to produce a reduced salinity hetero-azeotrope mixture and a feedstream salt product; and subjecting the reduced salinity hetero-azeotrope mixture to the distillation to produce the multi-phase condensate. 15. The method of claim 1 , in which the aqueous composition has an oil content of greater than 0.1 weight percent (wt. %) based on the total weight of the aqueous composition. 16. The method of claim 1 , in which the hetero-azeotrope mixture has a volume ratio of the aqueous composition to the entrainers of from 0.2 to 9.0. 17. The method of claim 1 , in which the hetero-azeotrope mixture has a hetero-azeotrope boiling temperature at an operating distillation pressure equal to atmospheric pressure at sea level (101.325 kilopascals (kPa)) of less than or equal to 100° C. 18. The method of claim 1 , in which the hetero-azeotrope mixture has a distillation temperature of less than or equal to 100° C. at the operating distillation pressure.

Assignees

Inventors

Classifications

  • using solar energy · CPC title

  • Water desalination · CPC title

  • from metallurgical processes, i.e. from the production, refining or treatment of metals, e.g. galvanic wastes · CPC title

  • from quarries or from mining activities · CPC title

  • Seawater, e.g. for desalination · CPC title

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What does patent US10874957B2 cover?
A method of desalinating an aqueous composition includes forming a hetero-azeotrope mixture by combining the aqueous composition with an entrainer, the aqueous composition including at least one salt, and subjecting the hetero-azeotrope mixture to distillation at a distillation temperature of less than the boiling temperature of the aqueous composition for an operating distillation pressure, re…
Who is the assignee on this patent?
Saudi Arabian Oil Co
What technology area does this patent fall under?
Primary CPC classification B01D3/36. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Dec 29 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 7 related publications on this page (citations in our corpus or others sharing the same primary CPC).