JP2010248609A - Lead electrolytic method (6) - Google Patents
Lead electrolytic method (6) Download PDFInfo
- Publication number
- JP2010248609A JP2010248609A JP2009206902A JP2009206902A JP2010248609A JP 2010248609 A JP2010248609 A JP 2010248609A JP 2009206902 A JP2009206902 A JP 2009206902A JP 2009206902 A JP2009206902 A JP 2009206902A JP 2010248609 A JP2010248609 A JP 2010248609A
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- JP
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- Prior art keywords
- lead
- electrolytic
- recovering
- smooth
- electrolytic method
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- 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
- 238000000034 method Methods 0.000 title claims abstract description 13
- 239000008151 electrolyte solution Substances 0.000 claims description 12
- 238000005868 electrolysis reaction Methods 0.000 claims description 4
- 238000004070 electrodeposition Methods 0.000 abstract description 5
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 abstract description 5
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 abstract description 3
- 239000011737 fluorine Substances 0.000 abstract description 3
- 229910052731 fluorine Inorganic materials 0.000 abstract description 3
- 239000002440 industrial waste Substances 0.000 abstract description 2
- 239000002994 raw material Substances 0.000 abstract description 2
- 238000007670 refining Methods 0.000 abstract description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
- 239000000155 melt Substances 0.000 abstract 2
- 239000000428 dust Substances 0.000 abstract 1
- 239000003792 electrolyte Substances 0.000 abstract 1
- 229910052742 iron Inorganic materials 0.000 abstract 1
- 239000000758 substrate Substances 0.000 abstract 1
- 238000000746 purification Methods 0.000 description 5
- 238000003723 Smelting Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000009499 grossing Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000779 smoke Substances 0.000 description 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- PIJPYDMVFNTHIP-UHFFFAOYSA-L lead sulfate Chemical compound [PbH4+2].[O-]S([O-])(=O)=O PIJPYDMVFNTHIP-UHFFFAOYSA-L 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
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
Landscapes
- Electrolytic Production Of Metals (AREA)
Abstract
Description
本発明は、非鉄製錬、基盤や電子部品などリサイクル原料の溶融炉、及び産業廃棄物を溶融処理する乾式炉より発生する乾式煙灰中に含まれているPbを回収する方法に関する。 The present invention relates to a method for recovering Pb contained in non-ferrous smelting, melting furnaces for recycled materials such as bases and electronic components, and dry smoke ash generated from a dry furnace for melting industrial waste.
非鉄製錬の乾式煙灰中に含まれているPbを回収するため、煙灰を硫酸浸出し、硫酸鉛にした後、電気炉で溶融還元を行う。溶融還元により分離されたメタルをソーダ処理し、その後、メタルをアノード鋳造した後、珪フッ素酸浴中にて電解精製するBetts法を用いることでPbを回収している。 In order to recover Pb contained in non-ferrous smelting dry smoke ash, the smoke ash is leached with sulfuric acid to lead sulfate and then smelted and reduced in an electric furnace. Pb is recovered by using the Betts method in which the metal separated by smelting is soda-treated, and then the metal is anode cast, followed by electrolytic purification in a silicofluoric acid bath.
Betts法において、例えば特開昭50−115120 高純度鉛の電解精製方法(特許文献1)に開示されているが、電解浴が珪フッ素酸であることから、排水にフッ素除去設備が必要である。
従来の技術に対して、フッ素除去設備を設置する必要なく、平滑な電着鉛を回収することができる鉛の電解方法を提供することを目的とする。本発明では、スルファミン酸浴で電解精製することで、板状の電着鉛として回収することができる。 It is an object of the present invention to provide a lead electrolysis method capable of recovering smooth electrodeposited lead without the need for installing a fluorine removal facility with respect to the prior art. In this invention, it can collect | recover as plate-shaped electrodeposited lead by carrying out electrolytic purification in a sulfamic acid bath.
本発明者等は、上記の課題を解決するため以下の発明を成した。
(1)電解液中にノイゲンBN-1390及び又はノイゲンBN-2560を1〜700mg/Lになるように添加することで平滑な電着鉛を回収する鉛の電解方法。
(2)上記(1)において、電流密度を100A/m2以下にすることにより平滑な電着鉛を回収する鉛の電解方法。
The present inventors made the following invention in order to solve the above-mentioned problems.
(1) A lead electrolysis method for recovering smooth electrodeposited lead by adding Neugen BN-1390 and / or Neugen BN-2560 to 1 to 700 mg / L in the electrolytic solution.
(2) The lead electrolysis method for recovering smooth electrodeposited lead by setting the current density to 100 A / m 2 or less in (1) above.
本発明によれば、
(1)鉛の電解精製において、適切な添加剤を投入することで、電着面が、平滑な電着鉛が容易に得られる方法を見出した。
According to the present invention,
(1) In the electrolytic refining of lead, a method has been found in which an electrodeposited lead having a smooth electrodeposition surface can be easily obtained by introducing an appropriate additive.
以下に本発明をさらに詳細に説明する。
原料は、本発明の鉛含有物は、鉛 70〜99mass%、錫 0.04mass%以下、ビスマス0〜30mass%含有する。
例えば、上記鉛含有物を、アノード鋳造をし、そのアノードを用いて電解精製を行う。アノードのサイズとしては、カソードのサイズに比べ小さくすることで、エッジ効果を防ぐことができ、平滑で良好な電着鉛を回収することができる。
更に、スルファミン酸を20から100g/L添加するとより平滑な電着鉛を得ることが出来る。
The present invention is described in further detail below.
The raw material contains 70 to 99 mass% lead, 0.04 mass% or less tin, and 0 to 30 mass% bismuth in the lead-containing material of the present invention.
For example, the lead-containing material is subjected to anode casting, and electrolytic purification is performed using the anode. By making the anode size smaller than the cathode size, the edge effect can be prevented, and smooth and good electrodeposited lead can be recovered.
Furthermore, smoother electrodeposited lead can be obtained by adding 20 to 100 g / L of sulfamic acid.
また平滑剤としては、ノイゲンBN-1390及び又はノイゲンBN-2560を1〜700mg/Lで電流密度100A/m2以下、好ましくは、50から100A/m2にすることで、平滑で良好な電着鉛を図1に示すように回収することができる。 Further, as a smoothing agent, Neugen BN-1390 and / or Neugen BN-2560 at 1 to 700 mg / L and a current density of 100 A / m 2 or less, preferably 50 to 100 A / m 2 , smooth and good electric current can be obtained. The lead can be recovered as shown in FIG.
(実施例1) 平滑な電着鉛を回収する方法
電解液の組成として、鉛濃度:80g/L、スルファミン酸濃度:20g/Lに調整した溶液に平滑剤としてノイゲンBN-1390を10mg/Lを添加する。
高Bi品位の鉛アノードと鉛の種板または、ステンレス板をカソードとして、交互に電槽に装入する。
カソードの大きさは、アノードに対して、20〜30mm程度大きくした方が、エッジ部への電流集中を緩和することができ、最適である。
電極装入後、電槽内に電解液を補充し、電解液の電槽内滞留時間が1時間程度になるように給液することで、電槽内の濃度分布を均等にする。
電解液の液温を、20〜30℃に調整後、電流密度100A/m2で通電することで、平滑な電着鉛を回収することができる。
Example 1 Method for Recovering Smooth Electrodeposited Lead As a composition of the electrolytic solution, 10 mg / L of Neugen BN-1390 was used as a smoothing agent in a solution adjusted to lead concentration: 80 g / L and sulfamic acid concentration: 20 g / L. Add.
The high-Bi grade lead anode and lead seed plate or stainless steel plate is used as the cathode, and the battery is inserted alternately.
It is optimal that the size of the cathode be about 20 to 30 mm larger than the anode because the current concentration on the edge portion can be reduced.
After the electrode is charged, the electrolytic solution is replenished in the battery case, and the concentration distribution in the battery case is made uniform by supplying the electrolyte solution so that the residence time of the electrolytic solution in the battery case is about 1 hour.
After adjusting the liquid temperature of the electrolytic solution to 20 to 30 ° C., smooth electrodeposited lead can be recovered by applying current at a current density of 100 A / m 2 .
(実施例2) 平滑な電着鉛を回収する方法
電解液の組成として、鉛濃度:80g/L、スルファミン酸濃度:20g/Lに調整した溶液に平滑剤としてノイゲンBN-1390を400〜700mg/Lを添加する。
高Bi品位の鉛アノードと鉛の種板または、ステンレス板をカソードとして、交互に電槽に装入する。
カソードの大きさは、アノードに対して、20〜30mm程度大きくした方が、エッジ部への電流集中を緩和することができ、最適である。
電極装入後、電槽内に電解液を補充し、電解液の電槽内滞留時間が1時間程度になるように給液することで、電槽内の濃度分布を均等にする。
電解液の液温を、20〜30℃に調整後、電流密度100A/m2で通電することで、平滑な電着鉛を回収することができる。
(Example 2) Method of recovering smooth electrodeposited lead As a composition of the electrolytic solution, 400 to 700 mg of Neugen BN-1390 as a smoothing agent in a solution adjusted to lead concentration: 80 g / L and sulfamic acid concentration: 20 g / L Add / L.
The high-Bi grade lead anode and lead seed plate or stainless steel plate is used as the cathode, and the battery is inserted alternately.
It is optimal that the size of the cathode be about 20 to 30 mm larger than the anode because the current concentration on the edge portion can be reduced.
After the electrode is charged, the electrolytic solution is replenished in the battery case, and the concentration distribution in the battery case is made uniform by supplying the electrolyte solution so that the residence time of the electrolytic solution in the battery case is about 1 hour.
After adjusting the liquid temperature of the electrolytic solution to 20 to 30 ° C., smooth electrodeposited lead can be recovered by applying current at a current density of 100 A / m 2 .
Claims (2)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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JP2009206902A JP4979752B2 (en) | 2009-03-23 | 2009-09-08 | Electrolysis method of lead (6) |
CN2010102315027A CN102011141A (en) | 2009-03-23 | 2010-07-15 | Lead electrolytic method |
KR1020100074810A KR20110027556A (en) | 2009-09-08 | 2010-08-03 | Method for electrolyzing lead |
KR1020130061629A KR20130069698A (en) | 2009-09-08 | 2013-05-30 | Method for electrolyzing lead |
Applications Claiming Priority (3)
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JP2009070105 | 2009-03-23 | ||
JP2009070105 | 2009-03-23 | ||
JP2009206902A JP4979752B2 (en) | 2009-03-23 | 2009-09-08 | Electrolysis method of lead (6) |
Publications (2)
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JP2010248609A true JP2010248609A (en) | 2010-11-04 |
JP4979752B2 JP4979752B2 (en) | 2012-07-18 |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2010248608A (en) * | 2009-03-23 | 2010-11-04 | Jx Nippon Mining & Metals Corp | Lead electrolytic method (1) |
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JP6453743B2 (en) * | 2014-12-03 | 2019-01-16 | Jx金属株式会社 | Method for electrolytic purification of lead using sulfamic acid bath |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0428893A (en) * | 1990-05-24 | 1992-01-31 | Ishihara Chem Co Ltd | Tin, lead of tin-lead alloy plating bath |
JPH0483894A (en) * | 1990-07-27 | 1992-03-17 | Ishihara Chem Co Ltd | Tin, lead or tin-lead alloy plating bath |
JPH0913189A (en) * | 1995-05-15 | 1997-01-14 | Elf Atochem North America Inc | Electrowinning of lead |
JP2000034593A (en) * | 1998-07-14 | 2000-02-02 | Daiwa Kasei Kenkyusho:Kk | Aqueous solution for reduction precipitation of metal |
JP2010248608A (en) * | 2009-03-23 | 2010-11-04 | Jx Nippon Mining & Metals Corp | Lead electrolytic method (1) |
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2009
- 2009-09-08 JP JP2009206902A patent/JP4979752B2/en active Active
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- 2010-07-15 CN CN2010102315027A patent/CN102011141A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0428893A (en) * | 1990-05-24 | 1992-01-31 | Ishihara Chem Co Ltd | Tin, lead of tin-lead alloy plating bath |
JPH0483894A (en) * | 1990-07-27 | 1992-03-17 | Ishihara Chem Co Ltd | Tin, lead or tin-lead alloy plating bath |
JPH0913189A (en) * | 1995-05-15 | 1997-01-14 | Elf Atochem North America Inc | Electrowinning of lead |
JP2000034593A (en) * | 1998-07-14 | 2000-02-02 | Daiwa Kasei Kenkyusho:Kk | Aqueous solution for reduction precipitation of metal |
JP2010248608A (en) * | 2009-03-23 | 2010-11-04 | Jx Nippon Mining & Metals Corp | Lead electrolytic method (1) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010248608A (en) * | 2009-03-23 | 2010-11-04 | Jx Nippon Mining & Metals Corp | Lead electrolytic method (1) |
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JP4979752B2 (en) | 2012-07-18 |
CN102011141A (en) | 2011-04-13 |
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