CN116119743A - Method for reducing sulfate radical in ball nickel product - Google Patents

Method for reducing sulfate radical in ball nickel product Download PDF

Info

Publication number
CN116119743A
CN116119743A CN202310230427.XA CN202310230427A CN116119743A CN 116119743 A CN116119743 A CN 116119743A CN 202310230427 A CN202310230427 A CN 202310230427A CN 116119743 A CN116119743 A CN 116119743A
Authority
CN
China
Prior art keywords
stirring
liquid alkali
30min
nickel
clarifying
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN202310230427.XA
Other languages
Chinese (zh)
Inventor
王维强
赵德
王文鹏
高文斌
赵述明
张慧慧
李晓
王霞
侯建国
高博
刘吉彤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jinchuan Group Nickel Cobalt Co ltd
Original Assignee
Jinchuan Group Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Jinchuan Group Co Ltd filed Critical Jinchuan Group Co Ltd
Priority to CN202310230427.XA priority Critical patent/CN116119743A/en
Publication of CN116119743A publication Critical patent/CN116119743A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G53/00Compounds of nickel
    • C01G53/04Oxides; Hydroxides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/30Particle morphology extending in three dimensions
    • C01P2004/32Spheres
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Treatment Of Water By Oxidation Or Reduction (AREA)
  • Manufacture And Refinement Of Metals (AREA)
  • Manufacture Of Metal Powder And Suspensions Thereof (AREA)

Abstract

The invention discloses a method for reducing sulfate radical in a ball nickel product, which comprises the following steps: 1) Adding liquid alkali into spherical nickel hydroxide, wherein the concentration of the liquid alkali is 20-40%, the adding amount is 0.3-0.5L/kg, stirring for at least 1h, clarifying for 30min, and discharging supernatant; (2) Adding liquid alkali with concentration of 20-70% and adding amount of 0.3-0.8L/kg for secondary stirring for at least 1 hr, clarifying for 30min, and discharging supernatant; (3) Adding 60 ℃ pure water with the addition amount of 8-16L/kg, and washing for at least 1h.

Description

Method for reducing sulfate radical in ball nickel product
Technical Field
The invention relates to the technical field of chemical industry, in particular to a method for reducing sulfate radical in a ball nickel product.
Background
In the chemical precipitation reaction, there is a small amount of SO 4 2- Ions and Na+ ions are adsorbed on nickel hydroxide, ni (OH) 2 Middle SO 4 2- An increase in the content of the same impurities causes Ni (OH) 2 The crystal structure of (a) is changed, the specific discharge capacity is reduced, and the electrode polarization is increased. Thus, ni (OH) is removed 2 On-board embedded and adsorbed SO 4 2- The content will optimize the spherical Ni (OH) 2 The performance is improved, and the product quality is improved. Ordinary centrifugal washing mode can only wash Ni (OH) 2 Surface sulfate cannot thoroughly wash the sulfate embedded inside.
Disclosure of Invention
Aiming at the technical problems, the invention provides a method for reducing sulfate radical in a spherical nickel product.
In order to achieve the above purpose, the technical scheme of the invention is as follows:
a method of reducing sulfate in a nickel ball product comprising the steps of:
(1) Adding liquid alkali into spherical nickel hydroxide, wherein the concentration of the liquid alkali is 20-40%, the adding amount is 0.3-0.5L/kg, stirring for at least 1h, clarifying for 30min, and discharging supernatant;
(2) Adding liquid alkali with concentration of 20-70% and adding amount of 0.3-0.8L/kg for secondary stirring for at least 1 hr, clarifying for 30min, and discharging supernatant;
(3) Adding 60 ℃ pure water with the addition amount of 8-16L/kg, and washing for at least 1h.
Wherein in the step (1), stirring is carried out for 1-2h.
Wherein in the step (2), stirring is carried out for 1-2h.
Wherein, in the step (3), the washing is carried out for 1-2h.
The beneficial effects of the invention are as follows:
(1) The invention can reduce sulfate radical in the ball nickel product to below 0.25 percent which is lower than national standard by 0.5 percent.
(2) The impurities such as sulfate can be increasedThe crystal structure of Ni (OH) 2 is changed, the discharge capacity is reduced, and the electrode polarization is increased. Ordinary centrifugal washing mode can only wash Ni (OH) 2 The sulfate on the surface can not thoroughly wash the sulfate embedded in the interior, and the method removes Ni (OH) by adopting a mode of alkali intrusion washing and pure water washing 2 The sulfate in the product is analyzed by XRD and a scanning electron microscope to obtain the sample with unchanged structure and smooth appearance after alkali invasion.
(3) SO in the current washing ball nickel products 4 2- The method mainly comprises a pure water washing method and a sodium carbonate solution washing method, wherein the pure water washing method can only wash off SO attached to the surface of the ball nickel 4 2- Part of SO embedded during synthesis 4 2- Cannot be washed out, which will lead to SO in the product 4 2- Higher, the washing with sodium carbonate solution will introduce new impurity CO 3 2- The invention uses 20-40% aqueous alkali to wash the ball nickel product twice, and fully stirs under alkaline condition, OH-in the aqueous alkali can embed SO into the ball nickel 4 2- The internal structure of the spherical nickel product contains hydroxide ions, SO that the original structure is not changed by the introduction of OH < - >, and SO is attached to the surface of the spherical nickel 4 2- Washing with pure water, SO that SO in the ball nickel product can be effectively reduced 4 2- And new impurities are not introduced, and the main taste of the ball nickel product is improved.
Detailed Description
The present invention will be further described in detail with reference to the following embodiments, in order to make the objects, technical solutions and advantages of the present invention more apparent. It should be understood that the description is only illustrative and is not intended to limit the scope of the invention. In addition, in the following description, descriptions of well-known structures and techniques are omitted so as not to unnecessarily obscure the present invention.
Example 1
A method of reducing sulfate in a nickel ball product comprising the steps of:
(1) Adding liquid alkali into spherical nickel hydroxide, wherein the concentration of the liquid alkali is 20%, the adding amount is 0.3L/kg, stirring for 1h, clarifying for 30min, and discharging supernatant;
(2) Adding liquid alkali with concentration of 20% and adding amount of 0.3L/kg for secondary stirring for 1 hr, clarifying for 30min, and discharging supernatant;
(3) Pure water at 60℃was added in an amount of 8L/kg, and the mixture was washed for 1 hour.
Example 2
A method of reducing sulfate in a nickel ball product comprising the steps of:
(1) Adding liquid alkali into spherical nickel hydroxide, wherein the concentration of the liquid alkali is 40%, the adding amount is 0.5L/kg, stirring for 2 hours, clarifying for 30 minutes, and discharging supernatant;
(2) Adding liquid alkali with the concentration of 70% and the addition amount of 0.8L/kg for 2 hours, clarifying for 30 minutes, and discharging supernatant;
(3) Pure water at 60℃was added in an amount of 16L/kg, and the mixture was washed for 2 hours.
Example 3
A method for reducing sulfate radical in a ball nickel product, which comprises the following specific steps:
(1) Adding 2kg of spherical nickel hydroxide into a 2.5L beaker, adding 1L of 30% liquid alkali, stirring for 1h, and clarifying for 30min to obtain supernatant;
(2) Adding 0.3L of 20% liquid alkali again, stirring for 1h, clarifying for 30min, and discharging supernatant;
(3) Adding 12L of pure water at 60 ℃ and stirring for 30min, wherein the content of spherical nickel sulfate radical is lower than 0.25 percent after washing by using the method.
Example 4
A method for reducing sulfate radical in a ball nickel product, which comprises the following specific steps:
(1) 3kg of spherical nickel hydroxide is added into a 5L beaker, 1.5L of 40% liquid alkali is added, stirring is carried out for 1h, and supernatant is discharged after 30 min;
(2) Adding liquid alkali with the concentration of 40% by weight of 1.5L again, stirring for 1h, clarifying for 30min, and discharging supernatant;
(3) Adding 60 ℃ pure water 30L, stirring for 30min, and washing by using the method until the content of the spherical nickel sulfate radical is lower than 0.25%.
Example 5
A method for reducing sulfate radical in a ball nickel product, which comprises the following specific steps:
(1) At 5m 3 500kg of spherical nickel hydroxide is added into a reaction kettle, 250L of 40% liquid alkali is added, stirring is carried out for 1h, and supernatant is discharged after 30min of clarification;
(2) Adding 150L of 30% liquid alkali again, stirring for 1h, clarifying for 30min, and discharging supernatant;
(3) Adding pure water at 60 ℃ for 4m 3 Stirring for 30min, and washing with the method to obtain ball nickel sulfate less than 0.25%.
It is to be understood that the above-described embodiments of the present invention are merely illustrative of or explanation of the principles of the present invention and are in no way limiting of the invention. Accordingly, any modification, equivalent replacement, improvement, etc. made without departing from the spirit and scope of the present invention should be included in the scope of the present invention. Furthermore, the appended claims are intended to cover all such changes and modifications that fall within the scope and boundary of the appended claims, or equivalents of such scope and boundary.

Claims (4)

1. A method for reducing sulfate in a nickel ball product comprising the steps of:
(1) Adding liquid alkali into spherical nickel hydroxide, wherein the concentration of the liquid alkali is 20-40%, the adding amount is 0.3-0.5L/kg, stirring for at least 1h, clarifying for 30min, and discharging supernatant;
(2) Adding liquid alkali with concentration of 20-70% and adding amount of 0.3-0.8L/kg for secondary stirring for at least 1 hr, clarifying for 30min, and discharging supernatant;
(3) Adding 60 ℃ pure water with the addition amount of 8-16L/kg, and washing for at least 1h.
2. A method for reducing sulfate in a nickel ball product according to claim 1, wherein in step (1), stirring is performed for 1-2 hours.
3. A method for reducing sulfate in a nickel ball product according to claim 1, wherein in step (2), stirring is performed for 1-2 hours.
4. A method for reducing sulfate in a nickel ball product according to claim 1, wherein in step (3), the ball is washed for 1-2 hours.
CN202310230427.XA 2023-03-11 2023-03-11 Method for reducing sulfate radical in ball nickel product Pending CN116119743A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202310230427.XA CN116119743A (en) 2023-03-11 2023-03-11 Method for reducing sulfate radical in ball nickel product

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202310230427.XA CN116119743A (en) 2023-03-11 2023-03-11 Method for reducing sulfate radical in ball nickel product

Publications (1)

Publication Number Publication Date
CN116119743A true CN116119743A (en) 2023-05-16

Family

ID=86302947

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202310230427.XA Pending CN116119743A (en) 2023-03-11 2023-03-11 Method for reducing sulfate radical in ball nickel product

Country Status (1)

Country Link
CN (1) CN116119743A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1383587A (en) * 2000-06-16 2002-12-04 松下电器产业株式会社 Anode active material for alkali storage battery, anode including samd, and alkali storage battery
CN101168453A (en) * 2006-10-27 2008-04-30 北京有色金属研究总院 Method for treating (SO4)2- impurity of spherical nickel hydroxide

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1383587A (en) * 2000-06-16 2002-12-04 松下电器产业株式会社 Anode active material for alkali storage battery, anode including samd, and alkali storage battery
CN101168453A (en) * 2006-10-27 2008-04-30 北京有色金属研究总院 Method for treating (SO4)2- impurity of spherical nickel hydroxide

Similar Documents

Publication Publication Date Title
CN101254935B (en) Method for preparing calcium hydroxide with high purity and high activity
CN107959023B (en) Preparation method of sulfur, nickel, cobalt and manganese three-element mixed hydroxide with low sodium content
CN109516479B (en) Preparation method of battery-grade lithium hydroxide
KR20120041750A (en) Method for etching of silicon surfaces
WO2023071353A1 (en) Method for removing fluorine in positive electrode leachate of lithium batteries
CN113683130B (en) Preparation method of nickel-rich large-particle-size ternary precursor with low sodium and sulfur impurity content
CN109592699B (en) Preparation method of battery-grade lithium hydroxide
CN111170342A (en) Preparation method of battery-grade anhydrous lithium hydroxide
CN116119743A (en) Method for reducing sulfate radical in ball nickel product
ES2956182A2 (en) Method for efficiently removing fluorine from spent lithium battery
CN112357942A (en) Method for improving whiteness of aluminum hydroxide product by Bayer process
CN103572317A (en) Method for refining electrolytic manganese dioxide product
CN109797283B (en) Hydrochloric acid leaching method for silicon-containing nickel hydroxide cobalt
CN110217806A (en) A kind of salt lake richness lithium making from brine for bulky grain lithium carbonate method
CN108179143B (en) Magnetic graphene oxide immobilized enzyme and application thereof in wet corn soaking
RU2179194C2 (en) Method of hydrometallurgy preparation of zinc oxide
CN109761253A (en) A kind of alumina producing decomposition and crystallization auxiliary agent
JPS582166B2 (en) Method for removing cobalt from aqueous nickel sulfate solution
CN115448358B (en) Method for removing iron in low-concentration industrial titanium liquid hydrolysis process
JP3493835B2 (en) Method for producing manganese dioxide and alkaline dry battery using the same
CN112441676A (en) Method for treating acid wastewater of titanium dioxide by sulfuric acid process
CN113088998B (en) Preparation method of electrolytic manganese dioxide for producing lithium manganate material
CN114875451B (en) Indium sulfate electrolyte and preparation method thereof
CN110697736A (en) Method for removing iodine from high-iodine primary brine in caustic soda production
RU2264481C1 (en) Method of production of gallium from alkali-aluminate solutions of aluminous production

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
TA01 Transfer of patent application right
TA01 Transfer of patent application right

Effective date of registration: 20240411

Address after: 737104 No. 2 Lanzhou Road, Beijing Road Street, Jinchuan District, Jinchang City, Gansu Province

Applicant after: Jinchuan Group Nickel Cobalt Co.,Ltd.

Country or region after: China

Address before: 737103 No. 98, Jinchuan Road, Jinchang, Gansu

Applicant before: JINCHUAN GROUP Co.,Ltd.

Country or region before: China