JPH0310031A - Method for extracting and separating cobalt from cobalt-nickel oxide - Google Patents
Method for extracting and separating cobalt from cobalt-nickel oxideInfo
- 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
Links
- 239000010941 cobalt Substances 0.000 title claims description 18
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 title claims description 18
- 229910017052 cobalt Inorganic materials 0.000 title claims description 17
- 238000000034 method Methods 0.000 title claims description 8
- KSHLPUIIJIOBOQ-UHFFFAOYSA-N [O--].[O--].[O--].[O--].[Co++].[Ni++] Chemical compound [O--].[O--].[O--].[O--].[Co++].[Ni++] KSHLPUIIJIOBOQ-UHFFFAOYSA-N 0.000 title 1
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 8
- -1 alkyl phosphoric acid Chemical compound 0.000 claims abstract description 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims abstract description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims abstract description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 14
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract description 6
- 238000003756 stirring Methods 0.000 abstract description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 abstract description 2
- 239000003513 alkali Substances 0.000 abstract description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract description 2
- 229910020630 Co Ni Inorganic materials 0.000 abstract 1
- 229910002440 Co–Ni Inorganic materials 0.000 abstract 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 6
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000000605 extraction Methods 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 229910000428 cobalt oxide Inorganic materials 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 230000035484 reaction time Effects 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- JJJOZVFVARQUJV-UHFFFAOYSA-N 2-ethylhexylphosphonic acid Chemical compound CCCCC(CC)CP(O)(O)=O JJJOZVFVARQUJV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000013626 chemical specie Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- NQVWGZIEECWBMO-UHFFFAOYSA-N didodecan-2-yl hydrogen phosphate Chemical compound CCCCCCCCCCC(C)OP(O)(=O)OC(C)CCCCCCCCCC NQVWGZIEECWBMO-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Landscapes
- Extraction Or Liquid Replacement (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
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.
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)
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.
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)
| 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)
| 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 |
-
1989
- 1989-06-06 JP JP1143899A patent/JPH0776394B2/en not_active Expired - Lifetime
Patent Citations (1)
| 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)
| 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 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |