JPH0310031A - Method for extracting and separating cobalt from cobalt-nickel oxide - Google Patents

Method for extracting and separating cobalt from cobalt-nickel oxide

Info

Publication number
JPH0310031A
JPH0310031A JP14389989A JP14389989A JPH0310031A JP H0310031 A JPH0310031 A JP H0310031A JP 14389989 A JP14389989 A JP 14389989A JP 14389989 A JP14389989 A JP 14389989A JP H0310031 A JPH0310031 A JP H0310031A
Authority
JP
Japan
Prior art keywords
cobalt
reaction
extracted
phosphoric acid
nickel
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.)
Granted
Application number
JP14389989A
Other languages
Japanese (ja)
Other versions
JPH0776394B2 (en
Inventor
Masakazu Aranae
新苗 正和
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.)
National Institute of Advanced Industrial Science and Technology AIST
Original Assignee
Agency of Industrial Science and Technology
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 Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology
Priority to JP1143899A priority Critical patent/JPH0776394B2/en
Publication of JPH0310031A publication Critical patent/JPH0310031A/en
Publication of JPH0776394B2 publication Critical patent/JPH0776394B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Extraction Or Liquid Replacement (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Abstract

PURPOSE:To unnecessitate the addition of an alkali from the outside and to contrive to save energy based on the occurrence of a reaction at a low temp. by directly dissolving Co to extract and separate from mixed oxide of Co and Ni by an organic soln. including alkyl phosphoric acid. CONSTITUTION:Co-Ni mixed oxide having the shape of CoO and NiO is brought into reaction with an organic soln. of aliphatic hydrocarbons, aromatic hydrocarbons, etc., including alkyl phosphoric acid such as bis-2-ethylhexyl phosphate at a prescribed stirring rate and a reaction temp. to selectively dissolve and extract Co. Then, after the completion of the reaction, the extracted Co is back-extracted by sulfuric acid or the like.

Description

【発明の詳細な説明】 従来の方法では、高温高圧下で、酸性溶液を月いて溶解
後、溶媒抽出法の適用できるPH領領域調節するためア
ルカリを加えなければならず、そのエネルギー及びアル
カリの消費量がそのプロセスの経済性を左右するという
開運がある。
DETAILED DESCRIPTION OF THE INVENTION In the conventional method, after dissolving an acidic solution under high temperature and high pressure, an alkali must be added to adjust the pH range to which the solvent extraction method can be applied. Fortunately, consumption determines the economics of the process.

[課題を解決するための手段] 本発明者は、アルキル燐酸を含む有機溶液を用いてやれ
ば、比較的低温でコバルト酸化物を溶解[従来技術コ 従来より、酸化鉱等より、コバルト及びニッケルを口取
する方法が検討されている.しかしそ九らは、主に硫酸
等の鉱酸により高温高圧下で溶解後、浸出液より溶媒抽
出法によりコバルトとニッケルを分離する方法である。
[Means for Solving the Problem] The present inventor has discovered that cobalt oxide can be dissolved at a relatively low temperature by using an organic solution containing alkyl phosphoric acid. A method of obtaining a share is being considered. However, these methods mainly involve dissolving cobalt and nickel with a mineral acid such as sulfuric acid under high temperature and pressure, and then using a solvent extraction method from the leachate to separate cobalt and nickel.

【発明が解決しようとする課題〕[Problem to be solved by the invention]

燐酸ビス−2−エチルヘキシルや、燐酸ビス−2一ドデ
シル等、アルキル基の炭素数が6以上のものが用いられ
る.これらを希釈する有機溶媒としては、アリキルmW
&と良く混じり合うものであればよく、このようなもの
としては、脂肪族炭化水素類や芳香族炭化水素類等が挙
げられる.また、コバルト酸化物及びニッケル酸化物は
各々Co。
Those having an alkyl group having 6 or more carbon atoms, such as bis-2-ethylhexyl phosphate and bis-2-dodecyl phosphate, are used. As an organic solvent for diluting these, alkyl mW
Any substance that mixes well with & may be used, such as aliphatic hydrocarbons and aromatic hydrocarbons. Moreover, the cobalt oxide and the nickel oxide are each Co.

及びNiOの形態を持つものである。and NiO.

本発明では、有機溶媒で希釈したアルキル燐酸をコバル
ト及びニッケル酸化物と反応させてコバルトを選択的に
溶解抽出するが、この場合、D2EHPA11度は1%
〜50%、好ましくは10%程度であり、反応温度は5
0”C以下、好ましくは30℃以下である0反応終了後
、抽出されたコバルトは硫酸で逆抽出する。
In the present invention, cobalt is selectively dissolved and extracted by reacting alkyl phosphoric acid diluted with an organic solvent with cobalt and nickel oxide, but in this case, D2EHPA 11 degrees is 1%
~50%, preferably about 10%, and the reaction temperature is 50%.
After completion of the reaction at a temperature below 0''C, preferably below 30°C, the extracted cobalt is back-extracted with sulfuric acid.

[発明の効果・用途] ル(D2EHPA)を含むキシレン溶液と各々固液1度
5g/l、粒度200me s h以下のコバルト及び
ニッケル酸化物を、攪はん速度900rpm、反応時間
72時間で反応させたときのコバルトとニッケルの抽出
率を表1に示す。また、抽出したコバルトの化学種を分
光光度針で調べた結果、四面体型の錯体を形成していた
[Effects/Applications of the Invention] A xylene solution containing D2EHPA was reacted with cobalt and nickel oxides each having a solid-liquid ratio of 5 g/l and a particle size of 200 mes h or less at a stirring speed of 900 rpm and a reaction time of 72 hours. Table 1 shows the extraction rates of cobalt and nickel. In addition, the chemical species of extracted cobalt was examined using a spectrophotometric needle, and it was found that it formed a tetrahedral complex.

表1 のプロセスに適している。しかも、アルキル燐酸を含む
有機溶液はコバルトの逆抽出後回利用できるなどの効果
がある。また1本発明はコバルトとニッケルの分離に好
適である。
Suitable for the processes in Table 1. Moreover, the organic solution containing alkyl phosphoric acid has the advantage that it can be used after cobalt back extraction. Furthermore, the present invention is suitable for separating cobalt and nickel.

[実施例] 次に本発明の実施例を示す。[Example] Next, examples of the present invention will be shown.

実施例1 容量濃度10%の燐酸ビス−2−エチルへキシ実施例2 容量濃度10%のD2EHPAを含むキシレン溶液と各
々固液濃度5g/l、粒度200mesh以下のコバル
ト及びニッケル酸化物を、攪はん速度900rpm、反
応温度zO℃で反応させたときの、コバルト及びニッケ
ルの抽出率に与える反応時間の影響を検討した結果を表
2に示す。
Example 1 Bis-2-ethylhexyl phosphate with a volume concentration of 10% Example 2 A xylene solution containing D2EHPA with a volume concentration of 10% and cobalt and nickel oxides each having a solid-liquid concentration of 5 g/l and a particle size of 200 mesh or less were stirred. Table 2 shows the results of examining the effect of reaction time on the extraction rate of cobalt and nickel when the reaction was carried out at a pumping speed of 900 rpm and a reaction temperature of zO<0>C.

表2 種々のD2EHPA11度のキシレン溶液と固液濃度5
 g / l、粒度200mesh以下のコバルト酸化
物を、攪はん速度900 r p m、  反応温度2
0℃、反応時間72時間で反応させたときのコバルトの
抽出率に与えるD2EHPA濃度の影響を表3に示す。
Table 2 Various D2EHPA 11 degree xylene solutions and solid-liquid concentration 5
g/l, cobalt oxide with a particle size of 200 mesh or less, stirring speed 900 rpm, reaction temperature 2
Table 3 shows the influence of the D2EHPA concentration on the cobalt extraction rate when the reaction was carried out at 0°C for a reaction time of 72 hours.

表3 表2かられかるように、反応温度20℃の場合30時間
過ぎから急速に反応が進んだ0反応温度が30℃のとき
は、50時間過ぎから反応が急速に進み、反応温度50
’Cのときは72時間反応させてもそれほど反応は進ま
なかった。
Table 3 As can be seen from Table 2, when the reaction temperature was 20°C, the reaction proceeded rapidly after 30 hours; when the reaction temperature was 30°C, the reaction proceeded rapidly after 50 hours;
In the case of 'C, the reaction did not progress much even after 72 hours of reaction.

実施例3 また、ニッケル酸化物に対して同様に検討したところ、
D2EHPA濃度の増加とともにその抽出性の低下がみ
られたが、いずれにしてもその抽出性は非常に低いもの
であった。
Example 3 In addition, a similar study was conducted on nickel oxide, and it was found that
As the D2EHPA concentration increased, its extractability decreased, but in any case, the extractability was very low.

[比較例] 2−エチルへキシルホスホン酸モノ−2−二チルヘキシ
ル(EHEHPA)の容量濃度10%のキシレン溶液を
各々固液濃度5g/l、粒度2゜Om e s h以下
のコバルト及びニッケル酸化物と、反応温度20℃、反
応時間72時間、攪はん速度900rpmで反応させた
とき、コバルトの抽出率は1.4%、ニッケルは0.3
%であった。また、反応温度、EHEHPAi1度の影
響はほとんど見られなかった。
[Comparative Example] A xylene solution of mono-2-ditylhexyl 2-ethylhexylphosphonate (EHEHPA) with a volume concentration of 10% was mixed with cobalt and nickel oxides each having a solid-liquid concentration of 5 g/l and a particle size of 2° Omesh or less. When the reaction temperature was 20℃, the reaction time was 72 hours, and the stirring speed was 900 rpm, the extraction rate of cobalt was 1.4% and that of nickel was 0.3%.
%Met. Moreover, almost no influence of the reaction temperature and EHEHPAi of 1 degree was observed.

Claims (1)

【特許請求の範囲】[Claims] 1、アルキル燐酸を含む有機溶液を用いてコバルト及び
ニッケル混合酸化物からコバルトを直接溶解抽出分離す
る方法。
1. A method for directly dissolving and extracting cobalt from cobalt and nickel mixed oxide using an organic solution containing alkyl phosphoric acid.
JP1143899A 1989-06-06 1989-06-06 Extraction and separation of cobalt from cobalt and nickel oxide Expired - Lifetime JPH0776394B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1143899A JPH0776394B2 (en) 1989-06-06 1989-06-06 Extraction and separation of cobalt from cobalt and nickel oxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1143899A JPH0776394B2 (en) 1989-06-06 1989-06-06 Extraction and separation of cobalt from cobalt and nickel oxide

Publications (2)

Publication Number Publication Date
JPH0310031A true JPH0310031A (en) 1991-01-17
JPH0776394B2 JPH0776394B2 (en) 1995-08-16

Family

ID=15349651

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1143899A Expired - Lifetime JPH0776394B2 (en) 1989-06-06 1989-06-06 Extraction and separation of cobalt from cobalt and nickel oxide

Country Status (1)

Country Link
JP (1) JPH0776394B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU667539B2 (en) * 1992-06-18 1996-03-28 Outokumpu Harjavalta Metals Oy Method for preventing the formation of jarosite and ammonium and alkali based double salts in solvent extraction circuits connected to acidic leaching processes

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53141176A (en) * 1977-05-14 1978-12-08 Daihachi Chem Ind Method of separating cobalt and nickel by solvent extraction

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53141176A (en) * 1977-05-14 1978-12-08 Daihachi Chem Ind Method of separating cobalt and nickel by solvent extraction

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU667539B2 (en) * 1992-06-18 1996-03-28 Outokumpu Harjavalta Metals Oy Method for preventing the formation of jarosite and ammonium and alkali based double salts in solvent extraction circuits connected to acidic leaching processes

Also Published As

Publication number Publication date
JPH0776394B2 (en) 1995-08-16

Similar Documents

Publication Publication Date Title
CN104726724B (en) The method that scandium is extracted from lateritic nickel ore
JPH10287864A (en) Method for recovering valuable metal from positive electrode active material for lithium ion secondary battery
CN103436715B (en) A method for extracting vanadium from stone coal
US12006227B2 (en) Nickel-iron wet treatment method and application thereof
JP2011230938A (en) Method of manufacturing crystalline iron arsenate starting material liquid from smoke and ash
Khorfan et al. Recovery of vanadium pentoxide from spent catalyst used in the manufacture of sulphuric acid
Xu et al. Mextral® 6103H/naphthenic acid/TOPO synergistic extraction system for recovery of nickel and cobalt from nickel laterite
CN107814375B (en) Fullerene water-soluble modifier and preparation method thereof
ZA200404077B (en) Integrated ammoniacal solvent extraction and hydrogen reduction of nickel.
CN106756013A (en) A kind of method of the direct nickel cobalt saponification of P204, P507
JPH0310031A (en) Method for extracting and separating cobalt from cobalt-nickel oxide
CN109266871B (en) Preparation method of submicron scandium oxide
JPS60245736A (en) Method for recovering gallium
JPH0310032A (en) Method for extracting and separating cobalt from cobalt-nickel oxide by organic-water solution including alkyl phosphoric acid
CN116002745A (en) A method for preparing mixed rare earth oxides from liquid after rare earth membrane enrichment
CN111333861B (en) A kind of extraction liquid of water-soluble humate in weathered coal and extraction method thereof
CN115626620A (en) Preparation method of manganese phosphate
CN115403072A (en) Preparation method of superparamagnetic composite nanoparticles
CN102476829B (en) A kind of preparation method of vanadyl sulfate
CN111961849A (en) Method for extracting and separating scandium
CN113774219A (en) Method for recycling waste cobalt-molybdenum hydrogenation catalyst
CN119845689B (en) Asynchronous enrichment and continuous determination of platinum and gold in ores
JPS616216A (en) Wet treatment of laterite ore
Nagel et al. The recovery of nickel and cobalt from a bioleach liquor saturated in calcium using versatic acid in a synergistic mixture with 4-nonyl pyridine
JP4389298B2 (en) Method for producing triethanolammonium nitrate

Legal Events

Date Code Title Description
EXPY Cancellation because of completion of term