JPS59118893A - Manufacture of electrolytic iron - Google Patents
Manufacture of electrolytic ironInfo
- Publication number
- JPS59118893A JPS59118893A JP57226565A JP22656582A JPS59118893A JP S59118893 A JPS59118893 A JP S59118893A JP 57226565 A JP57226565 A JP 57226565A JP 22656582 A JP22656582 A JP 22656582A JP S59118893 A JPS59118893 A JP S59118893A
- Authority
- JP
- Japan
- Prior art keywords
- bath
- electrolytic
- iron
- chloride
- hydrochloric acid
- 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
Classifications
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Abstract
Description
【発明の詳細な説明】
本発明は電解浴として塩化第1鉄と、塩化ナトリウム及
び又は塩化力IJ i含有する塩酸酸性浴を用いた電解
鉄の製造法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing electrolytic iron using a hydrochloric acid acidic bath containing ferrous chloride, sodium chloride and/or chloridizing power IJ i as an electrolytic bath.
電解鉄は通常の軟鋼に比べ各種不純物が格段と少いため
、磁性材料、電子材料、合金材料。Electrolytic iron contains far fewer impurities than ordinary mild steel, so it can be used as a magnetic material, electronic material, and alloy material.
試験研究用ベースメタル材料等高品位を要求される分野
に賞月されている。It has been awarded in fields that require high quality, such as base metal materials for testing and research.
しかし、最近の技術革新に伴い、特殊分野において超高
純度化、特定元素の超低含有化が望tiて来ているが鉄
材を陽極として用いる第一鉄イオンを含有する塩酸浴の
支持電解質としては硫酸アンモニウム又は塩化アンモニ
ウムが。However, with recent technological innovations, ultra-high purity and ultra-low content of specific elements are becoming desirable in special fields. is ammonium sulfate or ammonium chloride.
そのpI−1緩衝作用性、高電導性、第一鉄イオンの第
二鉄イオンへの酸化による浴変化を防止する安定化性、
電解鉄の内外層の組織の均−性等の点から専用さhて来
ているのが現状である。its pI-1 buffering properties, high conductivity, and stabilizing properties that prevent bath changes due to oxidation of ferrous ions to ferric ions;
At present, electrolytic iron has been specially designed in view of the uniformity of the structure of the inner and outer layers.
しかしこの浴構成成分を用いた場合、第1表に示すごと
く、陽極として純鉄を用いても各成分元素の含有量は、
一般軟鋼の場合と比べそれほどは低下せず比較的多(、
各成分元素の低減を望む需要分野には不満足なものであ
り、技術的改良が望まれて来た。However, when these bath components are used, as shown in Table 1, even if pure iron is used as the anode, the content of each component element is
Compared to general mild steel, the decrease is not as great and is relatively high (,
This is unsatisfactory for the field of demand that requires reduction of each component element, and technical improvements have been desired.
第 1 表 (単位:重量係)ここに各元
素は次の方法で分析したものでお札(以下同じ。)
C:燃焼−赤外線吸収法
S:同上
P:モリブデンずr吸光々度法
Si:同上
へ40:原子吸光々度法
(2u:同上
N:蒸留−インドフェノール吸光4度法ここに純鉄とは
一般用軟鋼を一度従来法で電解しfrV)、乾式法で精
練して得たものである。Table 1 (Unit: Weight) Here each element was analyzed using the following method (the same applies below) C: Combustion-infrared absorption method S: Same as above P: Molybdenum r Absorbance method Si: Same as above 40: Atomic absorption spectrophotometry (2u: Same as above N: Distillation-indophenol absorption 4 degree method Here, pure iron is obtained by electrolyzing general mild steel once using a conventional method (frV) and refining it using a dry method. It is.
本発明者等は各元素含有量の低減化について鋭意研究を
した結果、塩化第一鉄を含有する塩酸酸性浴に塩化ナト
リウム及び又は塩化カリを支持電解質として添加するこ
とにより従来に比し格段と優わに低不純物含量の電解鉄
を得ることに成功し、本発明を完成した。As a result of intensive research into reducing the content of each element, the present inventors found that by adding sodium chloride and/or potassium chloride as a supporting electrolyte to an acidic hydrochloric acid bath containing ferrous chloride, the content of each element can be reduced significantly compared to conventional methods. We succeeded in obtaining electrolytic iron with an extremely low impurity content, and completed the present invention.
即ち1本発明の要旨は、鉄材を陽極とし、塩化第一鉄を
電解浴主成分とする電解鉄の製造法において、塩酸酸性
電解浴に塩化す) IJウム及び又は塩化カリを添加す
る電解鉄の製造法にある。That is, 1. The gist of the present invention is a method for producing electrolytic iron in which an iron material is used as an anode and ferrous chloride is the main component of the electrolytic bath. It is in the manufacturing method.
以下、本発明の内容を更に詳しく説明する。Hereinafter, the content of the present invention will be explained in more detail.
陽極として用いる鉄材は、一般軟鋼でもよいが少しでも
純度を上げる目的で純鉄を用いても良い。陰極は電解鉄
が放電電着するものでステンレス製等の板状体もしくは
回転ドラムが従来法同様用いられる。The iron material used as the anode may be general mild steel, but pure iron may be used for the purpose of increasing the purity even a little. The cathode is one on which electrolytic iron is electrodeposited by discharge, and a plate-shaped body made of stainless steel or the like or a rotating drum is used as in the conventional method.
電解浴は、主要成分として塩化第一鉄と塩化ナトIIウ
ム及び又は塩化カリとを含有する塩酸酸性浴が用いられ
る力(、濃度け、塩化第一鉄が0.5〜1.5モル/l
好fL(u%0.8〜1.2モル#、jA化ナトリウム
及び又は塩化カリウムは、2〜4モル/l好ま[7(は
3〜3.5モル/lに調整、維持される。The electrolytic bath is a hydrochloric acid acidic bath containing ferrous chloride, sodium chloride, and/or potassium chloride as main components (with a concentration of 0.5 to 1.5 mol/min of ferrous chloride). l
Preferably fL (u% 0.8-1.2 mol #, jA sodium and/or potassium chloride is preferably adjusted and maintained at 2-4 mol/l [7).
こtlらの成分が上記範囲外の場合は、浴安定性の低下
を来たしf!:す、電気型導度を悪(したり、均質な電
解鉄収率を低下せしめたりして好ましくない。If these components are outside the above range, the bath stability will decrease and f! : It is undesirable because it causes poor electrical conductivity and reduces the yield of homogeneous electrolytic iron.
浴の可Iは、浴が塩酸浴であるkめ、酸性であるが、3
5〜4.5好ましくは3.8〜4.2が浴の安定性(F
e”トの安定性)とが製品電解鉄の均質性等の点で選ば
わる。The strength of the bath is that the bath is a hydrochloric acid bath, which is acidic, but 3
5-4.5 preferably 3.8-4.2 is the bath stability (F
(e) stability) is selected in terms of the homogeneity of the product electrolytic iron.
浴温は65〜90℃好1しくは7o〜80℃がpl(の
場合と同様の理由で選ばゎる。The bath temperature is selected to be 65 to 90°C, preferably 7o to 80°C for the same reason as in the case of PL.
以下実施側でもって本発明を説明する。The present invention will be explained below in terms of implementation.
実施例1
陽極け−11と純鉄を夫々用い、陰唇としてはステンレ
ス鋼製回転ドラムを用いた。Example 1 Anode cage 11 and pure iron were used, respectively, and a stainless steel rotating drum was used as the labia.
電解浴条件は、
FeC40,9〜1. Oモル/IIc塩酸浴)NaC
13モル/ 12 (塩酸浴)
pH4,1〜4.2
浴温 70〜75℃
電圧 3.5v
電流密度 2.5 A/dttlを維持しに0
電解の結果得らねた電解鉄の含有不純物を分析し、第2
表に各元素ごとに表示した。The electrolytic bath conditions were FeC40,9-1. O mol/IIc hydrochloric acid bath) NaC
13 mol/12 (hydrochloric acid bath) pH 4.1 to 4.2 Bath temperature 70 to 75°C Voltage 3.5 V Current density 2.5 A/dttl maintained at 0 Impurities contained in electrolytic iron not obtained as a result of electrolysis Analyze the second
Each element is shown in the table.
実施例2゜
実施例1においてNaClの代りにKCAを用いた以外
同条件で行った。その結果は第3表に示す。Example 2 The same conditions as in Example 1 were repeated except that KCA was used instead of NaCl. The results are shown in Table 3.
第 3 表 (単位:重量係)
実施例3゜
実施例1においてNaC7のモル数のL/2をKClで
置き換えた以外同条件で行った。Table 3 (Unit: Weight) Example 3 The same conditions as in Example 1 were repeated except that L/2 of the number of moles of NaC7 was replaced with KCl.
その結果は第4表に示す。The results are shown in Table 4.
第 4 表 (単位二重量係) ゛以上の実施例
の結果から明らかなごとく、本発明の電解浴を用いるこ
とにより不純物含量を極度に低下させうろことがわかっ
た。Table 4 (Unit duplex weight ratio) As is clear from the results of the above examples, it was found that the impurity content could be extremely reduced by using the electrolytic bath of the present invention.
特許出願人 昭和電工株式会社 代理人菊地精−Patent applicant: Showa Denko Co., Ltd. Agent Sei Kikuchi
Claims (3)
る電解鉄の製造法において、塩酸酸性電解浴に塩化す)
IJウム及びまたは塩化カリを添加することを特徴と
する電解鉄の製造方法。(1) In the manufacturing method of electrolytic iron in which iron material is used as an anode and ferrous chloride is the main component of the electrolytic bath, chlorination is carried out in a hydrochloric acid acidic electrolytic bath)
A method for producing electrolytic iron, characterized by adding IJium and/or potassium chloride.
いて35〜45に維持しつつ行う特許請求の範囲第1項
記載の電解鉄の製造方法。(2) PII f of the electrolytic bath: The method for producing electrolytic iron according to claim 1, which is carried out while maintaining the PII f at 35 to 45 using hydrochloric acid and caustic soda.
許請求の範囲第1項もしくは第2項記載の電解鉄の製造
法。(3) The method for producing electrolytic iron according to claim 1 or 2, which is carried out while maintaining the temperature of the electrolytic bath at 65 to 95°C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57226565A JPS59118893A (en) | 1982-12-27 | 1982-12-27 | Manufacture of electrolytic iron |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57226565A JPS59118893A (en) | 1982-12-27 | 1982-12-27 | Manufacture of electrolytic iron |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59118893A true JPS59118893A (en) | 1984-07-09 |
JPH0353394B2 JPH0353394B2 (en) | 1991-08-14 |
Family
ID=16847146
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57226565A Granted JPS59118893A (en) | 1982-12-27 | 1982-12-27 | Manufacture of electrolytic iron |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59118893A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007224400A (en) * | 2006-02-27 | 2007-09-06 | Sumitomo Metal Mining Co Ltd | Method of recovering electrolytic iron from aqueous ferric chloride solution |
-
1982
- 1982-12-27 JP JP57226565A patent/JPS59118893A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007224400A (en) * | 2006-02-27 | 2007-09-06 | Sumitomo Metal Mining Co Ltd | Method of recovering electrolytic iron from aqueous ferric chloride solution |
Also Published As
Publication number | Publication date |
---|---|
JPH0353394B2 (en) | 1991-08-14 |
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