JPH02172829A - Production of nickel carbonate or nickel oxide - Google Patents

Production of nickel carbonate or nickel oxide

Info

Publication number
JPH02172829A
JPH02172829A JP32859288A JP32859288A JPH02172829A JP H02172829 A JPH02172829 A JP H02172829A JP 32859288 A JP32859288 A JP 32859288A JP 32859288 A JP32859288 A JP 32859288A JP H02172829 A JPH02172829 A JP H02172829A
Authority
JP
Japan
Prior art keywords
nickel
nickel carbonate
solution
produce
carbonate
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
JP32859288A
Other languages
Japanese (ja)
Other versions
JPH0637308B2 (en
Inventor
Takao Hashimoto
孝夫 橋本
Shizuo Yamanaka
山中 静雄
Akio Shinjo
新城 昭夫
Shizuo Kishino
岸野 静夫
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.)
TAENAKA KOGYO KK
Nippon Steel Corp
Tanaka Kogyo Co Ltd
Original Assignee
TAENAKA KOGYO KK
Sumitomo Metal Industries Ltd
Tanaka Kogyo 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 TAENAKA KOGYO KK, Sumitomo Metal Industries Ltd, Tanaka Kogyo Co Ltd filed Critical TAENAKA KOGYO KK
Priority to JP32859288A priority Critical patent/JPH0637308B2/en
Publication of JPH02172829A publication Critical patent/JPH02172829A/en
Publication of JPH0637308B2 publication Critical patent/JPH0637308B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G53/00—Compounds of nickel
    • C01G53/06—Carbonates
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G53/00—Compounds of nickel
    • C01G53/04—Oxides
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00—Physical properties of inorganic compounds
    • C01P2006/80—Compositional purity

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

PURPOSE:To produce high purity nickel carbonate for plating at low cost by allowing NaOH solution to absorb CO2 to produce Na2CO3 solution and neutralizing this solution with refined NiSO4. CONSTITUTION:The NaOH solution is allowed to absorb CO2 gas in an absorption tower packed with packing to produce Na2CO3. Refined NiSO4 is added to produce NiCO3, which is then filtered, washed with water and dried to obtain high purity NiCO3. Further, high purity NiO can be obtained by decomposing the NiCO3 by heat.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、メツキ用などの高純度炭酸ニッケルまたは酸
化ニッケルの製造方法に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method for producing high-purity nickel carbonate or nickel oxide for plating and the like.

〔従来の技術〕[Conventional technology]

鋼板の耐蝕性向上のために、ニッケルまたはその合金メ
ツキは多く用いられている。
Nickel or its alloy plating is often used to improve the corrosion resistance of steel plates.

このメツキのNi源としては、通常炭酸ニッケル(N 
i COv )が用いられるが、メツキ性状を阻害させ
ないためには、Co、Fe、Cu、Pb。
The Ni source for this plating is usually nickel carbonate (N
i COv ) is used, but in order not to inhibit plating properties, Co, Fe, Cu, and Pb are used.

Cd等の不純物が無いか極く少量であることおよびC1
等の含有量が少いことが要請されている。
No or very small amount of impurities such as Cd and C1
It is required that the content of such substances is low.

高純度炭酸ニッケルの従来の製造法は、一般には、第2
図の工程に基いている。すなわち、Niマット(Nis
ニア2〜73%Ni)に対して空気、水および必要によ
りイオウを添加して加圧抽出50(、、その後濾過51
を行い残渣を除去して粗NiSO4を得、これを精製5
2し不純物を除去してN15O<純液を得て、その後工
業用ソーダ灰N a zc Offを添加し、炭酸化反
応53を行い、水を用いて濾過・水洗54し、NazS
O4廃水は肥料用原料に用いるなどし、その後ケーキ分
は乾燥55し、炭酸ニッケルNjCOzを得ている。
Conventional methods for producing high-purity nickel carbonate generally involve
It is based on the process shown in the figure. That is, Ni matte (Nis
2 to 73%Ni), air, water, and if necessary, sulfur are added to extract under pressure 50 (, then filtration 51).
The residue was removed to obtain crude NiSO4, which was purified in step 5.
2 and remove impurities to obtain a N15O<pure liquid, then add industrial soda ash Nazc Off, perform a carbonation reaction 53, filter and wash with water 54, and NazS
The O4 wastewater is used as a raw material for fertilizer, and the cake is then dried to obtain nickel carbonate NjCOz.

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

しかしながら、上記従来法において用いる工業用のソー
ダ灰は第1表に示すように、純度がきわめて悪く、所望
の高純度炭酸ニッケルを得ることができなかった。
However, as shown in Table 1, the industrial soda ash used in the above conventional method has extremely poor purity, making it impossible to obtain the desired high-purity nickel carbonate.

第1表(単位ppm) そこで本発明の主たる目的は、高純度炭酸ニッケルまた
は酸化ニッケルを安価に製造できる方法を提供すること
にある。
Table 1 (unit: ppm) Therefore, the main object of the present invention is to provide a method for producing high-purity nickel carbonate or nickel oxide at low cost.

〔課題を解決するための手段〕[Means to solve the problem]

上記課題を解決するための炭酸ニッケルの製造方法は、
NaOH水溶液にCO2ガスを吸収させてN a 2 
CO、溶液を得て、これに精製ZnSOsを添加して中
和し炭酸ニッケルを得ることを特徴とする。
The method for producing nickel carbonate to solve the above problems is as follows:
By absorbing CO2 gas into NaOH aqueous solution, Na 2
The method is characterized in that a solution of CO is obtained and purified ZnSOs is added thereto to neutralize it to obtain nickel carbonate.

また、本発明の酸化ニッケルの製造方法は、NaOH水
溶液にCOtガスを吸収させてNa□COj溶液を得て
、これに精製N t S Osを添加して中和し炭酸ニ
ッケルを得、次いでその炭酸ニッケルを熱分解して酸化
ニッケルを得ることを特徴とするものである。
Further, in the method for producing nickel oxide of the present invention, COt gas is absorbed into an NaOH aqueous solution to obtain a Na□COj solution, which is neutralized by adding purified N t S Os to obtain nickel carbonate. It is characterized by obtaining nickel oxide by thermally decomposing nickel carbonate.

〔作用〕[Effect]

本発明では、工業用ソーダ灰を用いることなく、NaO
H水溶液にCO2ガスを吸収させてNa 2 COyを
得ているので、かつその出発物質としてのNaOHは水
銀法や隔膜法によって得られ、きわめて高純度であるた
め得られるNa 2 COsも高純度となる。しかもN
aOHは安価であるため得られる炭酸亜鉛も安価となる
。
In the present invention, without using industrial soda ash, NaO
Since Na 2 COy is obtained by absorbing CO2 gas into an H aqueous solution, NaOH as a starting material is obtained by the mercury method or diaphragm method, and has extremely high purity, so the obtained Na 2 COs is also highly pure. Become. Moreover, N
Since aOH is inexpensive, the resulting zinc carbonate is also inexpensive.

〔発明の具体的構成〕[Specific structure of the invention]

以下本発明をさらに詳説する。 The present invention will be explained in more detail below.

第1図は本発明法の概要図である。FIG. 1 is a schematic diagram of the method of the present invention.

lは吸収塔であり、内部には充填材2が充填されている
。下部からはCO,ガスが吹き込まれ、上部からはNa
OH水溶液が散布され、降下する過程でCO2ガスと接
触してNaC0zとなり、これが下部から抜き出され中
和槽3に導かれる。
1 is an absorption tower, and the inside thereof is filled with a filler 2. CO and gas are blown from the bottom, and Na from the top.
The OH aqueous solution is sprayed and in the process of falling comes into contact with CO2 gas to form NaC0z, which is extracted from the lower part and led to the neutralization tank 3.

この中和槽3には精製N i S O4が添加され、(
1)式の中和反応が生じ、炭酸ニッケルの水溶液かえら
れる。
Purified N i S O4 is added to this neutralization tank 3, and (
1) The neutralization reaction of the formula occurs and the aqueous solution of nickel carbonate is changed.

Na2COi+N15O*→N1COz +Na25O
tかくして得られたN i CO3は濾過機などの結晶
分離機4により洗浄水を用いながら結晶として取り出す
。次いで乾燥機5により乾燥して高純度N i CO3
結晶としてうる。
Na2COi+N15O*→N1COz +Na25O
The N i CO3 thus obtained is taken out as crystals by a crystal separator 4 such as a filter using washing water. Next, it is dried in a dryer 5 to obtain high purity N i CO3.
Available as crystals.

ところで前記の精製N I S Oaとしては、本発明
では第2表に示す純度のものをいう。
By the way, in the present invention, the above-mentioned purified NIS Oa refers to one having a purity shown in Table 2.

第2表(単位ppm) 本発明において、前記得られた炭酸ニッケルから、酸化
ニッケルを得ようとする場合、炭酸ニッケルの熱分解温
度以上で環状炉等の熱分解手段6にて熱分解する。この
熱分解によって生じるCO2ガスは、返送路7を介して
吸収塔lに戻し循環使用するのが、供給路8を通る補給
C02ガス量が少くて足り好適である。
Table 2 (unit: ppm) In the present invention, when obtaining nickel oxide from the nickel carbonate obtained above, it is thermally decomposed in a thermal decomposition means 6 such as an annular furnace at a temperature higher than the thermal decomposition temperature of nickel carbonate. It is preferable that the CO2 gas produced by this thermal decomposition is returned to the absorption tower 1 via the return line 7 for circulation use, since the amount of supplementary CO2 gas passing through the supply line 8 is small.

〔実施例〕〔Example〕

次に未発明の実施例を示す。 Next, an uninvented example will be shown.

常温下で実験室においてZ、COlを製造した。Z, COI was produced in the laboratory at room temperature.

まず10gのNaOHを5%水溶液とし、pH13,7
のNaOH水溶液を得た。これとcOガスとを吸収塔に
て向流的に接触させ、pH;10.3のNaとCO5水
溶液を得た。
First, 10g of NaOH was made into a 5% aqueous solution, and the pH was adjusted to 13.7.
An aqueous NaOH solution was obtained. This was brought into contact with cO gas in a countercurrent manner in an absorption tower to obtain an aqueous solution of Na and CO5 with a pH of 10.3.

これに対して、上記第2表の純度で、かっN1含有量が
100 g//(7)Ni  SO4溶液40.0を添
加し、中和晶析した。そのときにおける終点pHは8.
4であった。
To this, 40.0 g//(7) of Ni SO4 solution with purity shown in Table 2 above and N1 content of 100 g//(7) was added for neutralization and crystallization. The end point pH at that time was 8.
It was 4.

その後、脱水、洗浄、乾燥してN i COi終点を9
g得た。その純度は、Co1CuおよびPbのいずれも
1 ppm以下で、C/分も10ppm以下であった。
After that, dehydration, washing, and drying are performed to reduce the N i COi end point to 9
I got g. The purity of both Co1Cu and Pb was 1 ppm or less, and the C/min was 10 ppm or less.

次イテ、この9gのN i COsノ結晶を600′C
。
Next, heat this 9g of N i COs crystals to 600'C.
.

1時間、環状炉にて熱分解したところ、5gのNiO結
晶が得られた。その純度を第3表に示す。
After thermal decomposition in an annular furnace for 1 hour, 5 g of NiO crystals were obtained. Its purity is shown in Table 3.

第3表(単位ppm) 〔比較例〕 第1表に示す純度(単位ppm)の工業用ソーダ灰を用
いて、(11式の反応により炭酸ニッケルを得て、これ
を脱水、洗浄および乾燥してN r COyの結晶を得
たところ、その純度(単位ppm)は第4表の通りであ
った。
Table 3 (unit: ppm) [Comparative example] Using industrial soda ash having the purity (unit: ppm) shown in Table 1, nickel carbonate was obtained by the reaction of equation 11, which was dehydrated, washed and dried. When crystals of N r COy were obtained, the purity (unit: ppm) was as shown in Table 4.

第4表(単位ppm ) 〔発明の効果〕 以上の通り、本発明によれば、高純度炭酸ニッケルまた
は酸化ニッケルを簡素な工程を経てしかも安価に製造で
きる。
Table 4 (Unit: ppm) [Effects of the Invention] As described above, according to the present invention, high purity nickel carbonate or nickel oxide can be produced through simple steps and at low cost.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明のフローシートの例示図、第2図は従来
の炭酸ニッケルの製造法のフローシートである。 l ・・・ 吸収塔    2.3  ・・・ 中和槽
4 ・・・ 結晶分離機  5 ・・・ 乾燥機6 ・
・・ 熱分解手段 特許出願人住友金属工業株式会社 妙中鉱業株式会社 代 理 人 弁理士 永 井 義 久 NtCO:s 手続補正書 (自発) 1゜ 事件の表示 昭和63年 特許願 第328592号 2゜ 発明の名称 炭酸ニッケルまたは酸化ニッケルの製造方法3゜ 補正をする者 事件との関係
FIG. 1 is an exemplary flow sheet of the present invention, and FIG. 2 is a flow sheet of a conventional method for producing nickel carbonate. l ... Absorption tower 2.3 ... Neutralization tank 4 ... Crystal separator 5 ... Dryer 6 ・
... Pyrolysis means patent applicant Sumitomo Metal Industries Co., Ltd. Taenaka Mining Co., Ltd. Agent Patent attorney Yoshihisa Nagai NtCO:s Procedural amendment (spontaneous) 1゜Indication of case 1988 Patent Application No. 328592 2゜Name of the invention Process for producing nickel carbonate or nickel oxide 3゜Relationship with the case of the person making the amendment

Claims (2)

【特許請求の範囲】[Claims] (1)NaOH水溶液にCO_2ガスを吸収させてNa
_2CO_3溶液を得て、これに精製NiSO_4を添
加して中和し炭酸ニッケルを得ることを特徴とする炭酸
ニッケルの製造方法。
(1) By absorbing CO_2 gas into NaOH aqueous solution,
A method for producing nickel carbonate, which comprises obtaining a _2CO_3 solution and neutralizing it by adding purified NiSO_4 to obtain nickel carbonate.
(2)NaOH水溶液にCO_2ガスを吸収させてNa
_2CO_3溶液を得て、これに精製NiSO_4を添
加して中和し炭酸ニッケルを得、次いでその炭酸ニッケ
ルを熱分解して酸化ニッケルを得ることを特徴とする酸
化ニッケルの製造方法。
(2) By absorbing CO_2 gas into NaOH aqueous solution,
A method for producing nickel oxide, which comprises obtaining a _2CO_3 solution, neutralizing it by adding purified NiSO_4 to obtain nickel carbonate, and then thermally decomposing the nickel carbonate to obtain nickel oxide.
JP32859288A 1988-12-26 1988-12-26 Method for producing nickel carbonate or nickel oxide Expired - Lifetime JPH0637308B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32859288A JPH0637308B2 (en) 1988-12-26 1988-12-26 Method for producing nickel carbonate or nickel oxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32859288A JPH0637308B2 (en) 1988-12-26 1988-12-26 Method for producing nickel carbonate or nickel oxide

Publications (2)

Publication Number Publication Date
JPH02172829A true JPH02172829A (en) 1990-07-04
JPH0637308B2 JPH0637308B2 (en) 1994-05-18

Family

ID=18211997

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32859288A Expired - Lifetime JPH0637308B2 (en) 1988-12-26 1988-12-26 Method for producing nickel carbonate or nickel oxide

Country Status (1)

Country Link
JP (1) JPH0637308B2 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012129628A3 (en) * 2011-03-25 2013-06-27 Vale S/A Process for production of nickel carbonate"
WO2013145909A1 (en) * 2012-03-29 2013-10-03 住友金属鉱山株式会社 Method for producing high-purity nickel sulfate
US8969606B2 (en) 2011-06-10 2015-03-03 Invista North America S.A R.L. Calcination and reduction process including a fluidizing bed reactor
US9371343B2 (en) 2009-12-18 2016-06-21 Invista North America S.A. R.L. Nickel metal compositions and nickel complexes derived from basic nickel carbonates
US9371346B2 (en) 2010-09-07 2016-06-21 Invista North America S.A.R.L. Preparing a nickel phosphorus ligand complex
CN113044895A (en) * 2019-12-27 2021-06-29 荆门市格林美新材料有限公司 Preparation method of low-impurity high-nickel basic nickel carbonate
WO2025059834A1 (en) * 2023-09-19 2025-03-27 广东邦普循环科技有限公司 Preparation method for nickel sulfate and use thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0838627A (en) * 1994-08-04 1996-02-13 Meiwa Gravure Kk Band-shaped body for magnetic traetment

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9371343B2 (en) 2009-12-18 2016-06-21 Invista North America S.A. R.L. Nickel metal compositions and nickel complexes derived from basic nickel carbonates
US9371346B2 (en) 2010-09-07 2016-06-21 Invista North America S.A.R.L. Preparing a nickel phosphorus ligand complex
RU2585021C2 (en) * 2011-03-25 2016-05-27 Вале С/А Method of producing nickel carbonate
CN103443030A (en) * 2011-03-25 2013-12-11 淡水河谷公司 Production method of nickel carbonate
JP2014511813A (en) * 2011-03-25 2014-05-19 ヴァーレ、ソシエダージ、アノニマ Method for producing nickel carbonate
WO2012129628A3 (en) * 2011-03-25 2013-06-27 Vale S/A Process for production of nickel carbonate"
US8969606B2 (en) 2011-06-10 2015-03-03 Invista North America S.A R.L. Calcination and reduction process including a fluidizing bed reactor
JP2013203646A (en) * 2012-03-29 2013-10-07 Sumitomo Metal Mining Co Ltd Method for producing high-purity nickel sulfate
WO2013145909A1 (en) * 2012-03-29 2013-10-03 住友金属鉱山株式会社 Method for producing high-purity nickel sulfate
US9702023B2 (en) 2012-03-29 2017-07-11 Sumitomo Metal Mining Co., Ltd. Method for producing high-purity nickel sulfate
CN113044895A (en) * 2019-12-27 2021-06-29 荆门市格林美新材料有限公司 Preparation method of low-impurity high-nickel basic nickel carbonate
CN113044895B (en) * 2019-12-27 2023-09-05 荆门市格林美新材料有限公司 Preparation method of low-impurity high-nickel basic nickel carbonate
WO2025059834A1 (en) * 2023-09-19 2025-03-27 广东邦普循环科技有限公司 Preparation method for nickel sulfate and use thereof

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Publication number Publication date
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