Mineralization method of calcium chloride-type from lithium-containing salt lake brine by evaporation and brine mixing

US2024262704A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2024262704-A1
Application numberUS-202218260031-A
CountryUS
Kind codeA1
Filing dateAug 26, 2022
Priority dateFeb 28, 2022
Publication dateAug 8, 2024
Grant date

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Abstract

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The invention discloses a mineralization method of a calcium chloride-type from lithium-containing salt lake brine by evaporation and brine mixing, comprising the following steps of: (1) naturally evaporating the calcium chloride-type from lithium-containing salt lake brine to precipitate sodium salt and potassium-containing mixed salt; and (2) when calcium in the brine is saturated, adding saturated solution of magnesium chloride in a certain proportion for brine mixing operation, and then naturally evaporating to precipitate carnallite, wherein a lithium-containing old brine with low potassium and sodium contents is obtained when magnesium in the brine is saturated. The method has the characteristics of simple process, simple and convenient operation, high potassium yield and easy extraction of lithium from lithium-containing brine, and has practical significance for the development and utilization of potassium and lithium resources in calcium chloride salt lakes.

First claim

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1 . A mineralization method of a calcium chloride-type lithium-containing salt lake brine by evaporation and brine mixing, comprising the following steps of: (1) naturally evaporating a calcium chloride-type lithium-containing salt lake brine to precipitate a sodium salt and a potassium-containing mixed salt; and (2) adding a saturated solution of magnesium chloride in a proportion into the brine when calcium is saturated for brine mixing, and then performing naturally evaporation to precipitate carnallite, wherein a lithium-containing old brine with low potassium and sodium contents is obtained when magnesium in the brine is saturated; wherein in step (1), the calcium chloride-type lithium-containing salt lake brine is located in a potassium chloride area in a phase diagram of a quinary salt-water system Na + , K + , Mg 2+ , Ca 2+ //Cl − —H 2 O, at 25° C., and a mass ratio of Ca/Mg is 2 to 50; wherein in step (2), a proportion for brine mixing is such that the saturated solution of magnesium chloride is added according to a total Mg/K molar ratio of a calcium-saturated brine and the saturated solution of magnesium chloride of 2 to 10; and when magnesium in the brine is saturated, the brine with K + between 0.5 g/L and 5 g/L, Ca 2+ between 140 g/L and 200 g/L and Mg 2+ between 30 g/L and 80 g/L is the lithium-containing old brine with low potassium and sodium contents. 2 . The mineralization method of the calcium chloride-type lithium-containing salt lake brine by evaporation and brine mixing according to claim 1 , wherein in step (1), after the calcium chloride-type lithium-containing salt lake brine is naturally evaporated to precipitate sodium chloride, when potassium in the brine in a sodium chloride pool is saturated, the brine is pumped into a potassium mixed salt pool for evaporating continuously to precipitate the potassium-containing mixed salt. 3 . (canceled) 4 . The mineralization method of the calcium chloride-type lithium-containing salt lake brine by evaporation and brine mixing according to claim 2 , wherein in step (1), when the potassium in the brine is saturated, K + is between 23 g/L and 28 g/L, Ca 2+ is between 120 g/L and 180 g/L, and Mg 2+ is between 3 g/L and 8 g/L. 5 . The mineralization method of the calcium chloride-type lithium-containing salt lake brine by evaporation and brine mixing according to claim 1 , wherein in step (2), when the calcium in the brine is saturated, K + is between 22 g/L and 35 g/L, Ca 2+ is between 140 g/L and 240 g/L, and Mg 2+ is between 4 g/L and 9 g/L. 6 . (canceled) 7 . The mineralization method of the calcium chloride-type lithium-containing salt lake brine by evaporation and brine mixing according to claim 1 , wherein in step (2), the proportion for brine mixing is such that the saturated solution of magnesium chloride is added according to a total Mg/K molar ratio of the calcium-saturated brine and the saturated magnesium chloride solution of 2.5 to 7.5. 8 . (canceled) 9 . A lithium-containing old brine prepared by the mineralization method according to claim 1 . 10 . A battery-grade lithium carbonate, wherein the battery-grade lithium carbonate is obtained by a method comprising: separating the lithium-containing old brine of claim 9 by an electrodialysis membrane method or a nanofiltration membrane, then subjecting to evaporation and concentration, impurity removal and lithium precipitation to obtain a crude lithium carbonate, and then washing, drying and demagnetizing the crude lithium carbonate. 11 . A lithium-containing old brine prepared by the mineralization method according to claim 2 . 12 . (canceled) 13 . A lithium-containing old brine prepared by the mineralization method according to claim 4 . 14 . A lithium-containing old brine prepared by the mineralization method according to claim 5 . 15 . (canceled) 16 . A lithium-containing old brine prepared by the mineralization method according to claim 7 . 17 . (canceled) 18 . A battery-grade lithium carbonate, wherein the battery-grade lithium carbonate is obtained by a method comprising: separating the lithium-containing old brine of claim 11 by an electrodialysis membrane method or a nanofiltration membrane, then subjecting to evaporation and concentration, impurity removal and lithium precipitation to obtain a crude lithium carbonate, and then washing, drying and demagnetizing the crude lithium carbonate. 19 . A battery-grade lithium carbonate, wherein the battery-grade lithium carbonate is obtained by a method comprising: separating the lithium-containing old brine of claim 13 by an electrodialysis membrane method or a nanofiltration membrane, then subjecting to evaporation and concentration, impurity removal and lithium precipitation to obtain a crude lithium carbonate, and then washing, drying and demagnetizing the crude lithium carbonate. 20 . A battery-grade lithium carbonate, wherein the battery-grade lithium carbonate is obtained by a method comprising: separating the lithium-containing old brine of claim 14 by an electrodialysis membrane method or a nanofiltration membrane, then subjecting to evaporation and concentration, impurity removal and lithium precipitation to obtain a crude lithium carbonate, and then washing, drying and demagnetizing the crude lithium carbonate. 21 . A battery-grade lithium carbonate, wherein the battery-grade lithium carbonate is obtained by a method comprising: separating the lithium-containing old brine of claim 16 by an electrodialysis membrane method or a nanofiltration membrane, then subjecting to evaporation and concentration, impurity removal and lithium precipitation to obtain a crude lithium carbonate, and then washing, drying and demagnetizing the crude lithium carbonate.

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Classifications

  • Obtaining lithium · CPC title

  • C01D15/08Primary

    Carbonates; Bicarbonates · CPC title

  • C01D3/06Primary

    Preparation by working up brines; seawater or spent lyes · CPC title

  • C01D7/26Primary

    by precipitation or adsorption · CPC title

  • Chlorides · CPC title

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What does patent US2024262704A1 cover?
The invention discloses a mineralization method of a calcium chloride-type from lithium-containing salt lake brine by evaporation and brine mixing, comprising the following steps of: (1) naturally evaporating the calcium chloride-type from lithium-containing salt lake brine to precipitate sodium salt and potassium-containing mixed salt; and (2) when calcium in the brine is saturated, adding sat…
Who is the assignee on this patent?
Guangdong Brunp Recycling Technology Co Ltd, Hunan Brunp Recycling Tech Co Ltd, Hunan Brunp Ev Recycling Co Ltd
What technology area does this patent fall under?
Primary CPC classification C01D15/08. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Aug 08 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).