JPS6357799A - How to treat plating liquid - Google Patents
How to treat plating liquidInfo
- Publication number
- JPS6357799A JPS6357799A JP19871186A JP19871186A JPS6357799A JP S6357799 A JPS6357799 A JP S6357799A JP 19871186 A JP19871186 A JP 19871186A JP 19871186 A JP19871186 A JP 19871186A JP S6357799 A JPS6357799 A JP S6357799A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- chelate resin
- plating
- type
- ions
- 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.)
- Pending
Links
- 238000007747 plating Methods 0.000 title claims abstract description 42
- 239000007788 liquid Substances 0.000 title description 5
- 239000011347 resin Substances 0.000 claims abstract description 44
- 229920005989 resin Polymers 0.000 claims abstract description 44
- 239000013522 chelant Substances 0.000 claims abstract description 30
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical group OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 claims abstract description 8
- 125000000524 functional group Chemical group 0.000 claims abstract description 5
- 238000000034 method Methods 0.000 claims description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
- 150000002500 ions Chemical class 0.000 abstract description 24
- 239000002253 acid Substances 0.000 abstract description 10
- 229910001385 heavy metal Inorganic materials 0.000 abstract description 7
- 230000008929 regeneration Effects 0.000 abstract description 7
- 238000011069 regeneration method Methods 0.000 abstract description 7
- 230000006866 deterioration Effects 0.000 abstract description 4
- 239000012535 impurity Substances 0.000 abstract description 4
- 239000000243 solution Substances 0.000 description 28
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000000356 contaminant Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- -1 carbon ions Chemical class 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000002522 swelling effect Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Treatment Of Water By Ion Exchange (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は各種メッキ液中に含まれる夾雑イオンであるN
i、Fe、Cr、Cu等の重金属をキレート樹脂により
選択的に除去するメッキ液の処理方法に関する。[Detailed Description of the Invention] <Industrial Application Field> The present invention is directed to N, which is a contaminant ion contained in various plating solutions.
The present invention relates to a method for treating a plating solution in which heavy metals such as i, Fe, Cr, and Cu are selectively removed using a chelate resin.
〈従来技術〉
各種メッキ液中にはメッキ金属イオン等が多量に含有さ
れているため、その廃液処理や有価成分の回収には多大
の労力を要する。このため、最近では省資源並びに環境
汚染防止の立場から、メッキ処理工程はクローズド化さ
れつつあり、メッキ液の排出を極力抑えるとともにメッ
キ溶液から不純物を除去し、再利用する努力がなされて
いる。このようなりローズドシステムの採用により、メ
ッキ液中にはメッキ液の種類によりN1イオンを始めと
してFeイオン、 Crイオン、Cuイオン等の夾雑イ
オンが増加、蓄積されてくる。これらの夾雑イオンはメ
ッキ処理を妨害し、処理効率を低下される上、得られる
メッキ製品の品質不良の原因となる。そのため、こ九ら
夾雑イオン、 なかんず<Niイオンを除去する方法と
してキレート樹脂をNa形で使用する方法が知られてい
る。<Prior Art> Since various plating solutions contain large amounts of plating metal ions, etc., a great deal of effort is required to treat the waste solutions and recover valuable components. For this reason, in recent years, plating processes have been becoming more closed in order to conserve resources and prevent environmental pollution, and efforts are being made to minimize the discharge of plating solutions, remove impurities from plating solutions, and reuse them. By adopting such a closed system, contaminant ions such as N1 ions, Fe ions, Cr ions, and Cu ions increase and accumulate in the plating solution, depending on the type of plating solution. These contaminant ions interfere with the plating process, lowering the process efficiency and causing poor quality of the resulting plated product. Therefore, a method of using a chelate resin in the Na form is known as a method for removing these contaminant ions, especially <Ni ions.
〈発明が解消しようとする問題点〉
しかしながら、上述の如きNa形のキレート樹脂により
夾雑−rオンを除去する方法では、夾雑イオンを捕捉し
たキレート樹脂を再生するのに酸による溶離工程の後に
N a OHを使用するため、ランニングコストが大き
くなり、この際に樹脂の膨潤、収縮が大きくなるととも
に樹脂が破砕されやすく、長期使用の場合には樹脂の劣
化が大きくなるという問題点を有するものであった。<Problems to be Solved by the Invention> However, in the method of removing contaminant -r ions using Na-type chelate resin as described above, in order to regenerate the chelate resin that has captured the contaminant ions, N is required after the elution step with acid. Since a OH is used, the running cost is high, and at this time, the swelling and contraction of the resin increases, the resin is easily crushed, and there is a problem that the deterioration of the resin increases in the case of long-term use. there were.
く問題点を解決するための手段〉
本発明はキレート樹脂の再生にNaOHを使用せざるを
得ないNa形のキレート樹脂のかわりに、イミノジ酢酸
基を官能基にもつH形のキレート樹脂を用い、これをメ
ッキ液と接触させることにその特徴を有するものである
。Means for Solving the Problems> The present invention uses an H-type chelate resin having an iminodiacetic acid group as a functional group instead of a Na-type chelate resin that requires the use of NaOH to regenerate the chelate resin. , which is characterized by its contact with a plating solution.
これらイミノジ酢酸基を官能基にもつH形のキレート樹
脂とメッキ液との接触はキレート樹脂を充填したカラム
にメッキ液を下向流で通液することにより行われ、これ
によりメッキ液中のNiイオン等の重金属が選択的に捕
捉される。Contact between these H-type chelate resins, which have iminodiacetic acid groups as functional groups, and the plating solution is carried out by passing the plating solution in a downward flow through a column filled with the chelate resin. Heavy metals such as ions are selectively captured.
これら重金属が除去されたメッキ液はメッキ槽内に戻し
、メッキ処理を続行する。なお、イミノジ酢酸基の官能
基系キレート樹脂をH形で使用する場合、樹脂のPHが
低いために重金属とキレートを形成しにくいのが一般的
であるが、本発明における処理液はメッキ液であるため
。The plating solution from which these heavy metals have been removed is returned to the plating bath to continue the plating process. In addition, when a functional group-based chelate resin with iminodiacetic acid group is used in the H form, it is generally difficult to form a chelate with heavy metals due to the low pH of the resin, but the processing solution in the present invention is a plating solution. Because there is.
通常リン酸二水素ナトリウム(N a H2P O4)
等の電解液溶液であり、pH4〜5を示し、このバッフ
ァ効果により、キレート樹脂とメッキ液とが接触する際
、pHが3以上に保持され、Ni等の夾雑イオンが樹脂
とキレートを形成し易くなって捕捉されると考えられる
。Usually sodium dihydrogen phosphate (N a H2P O4)
It is an electrolyte solution with a pH of 4 to 5, and due to this buffer effect, when the chelate resin and the plating solution come into contact, the pH is maintained at 3 or higher, and contaminant ions such as Ni form chelates with the resin. It is thought that it will become easier to be captured.
このようにしてキレート樹脂と所定量のメッキ液とを接
触させて、メッキ液中の夾雑物イオンをキレート樹脂に
より捕捉した後は、キレート樹脂を再生するようにする
。この夾雑イオンを捕捉したキレート樹脂の再生は酸を
用いる。After the chelate resin and a predetermined amount of the plating solution are brought into contact with each other in this manner and the impurity ions in the plating solution are captured by the chelate resin, the chelate resin is regenerated. An acid is used to regenerate the chelate resin that has captured the contaminant ions.
酸としてはHCQ、H2SO4,HNO,が考えられる
が、HCQを使用すると処理液中にC息イオンが残留し
てメッキ処理時に悪影響を与えるようになるため、H2
SO4を使用することが好ましい。これら、酸による樹
脂の再生はカラムへのメッキ液の通液を中止し、酸の希
釈槽からポンプにより酸をカラム内へ通すことで行われ
る。なお、再生レベルはH2SO4で150〜250g
H,SQ、/Q−R,HCQで110〜200gHCQ
/Q−Rである。Possible acids include HCQ, H2SO4, and HNO; however, if HCQ is used, carbon ions will remain in the processing solution, which will have an adverse effect on the plating process.
Preferably, SO4 is used. These regenerations of the resin using acid are performed by stopping the flow of plating solution into the column and passing acid from the acid dilution tank into the column using a pump. The regeneration level is 150-250g for H2SO4.
110-200g HCQ for H, SQ, /Q-R, HCQ
/QR.
〈作 用〉
以上のように本発明においては、イミノジ酢酸基系キレ
ート樹脂をH形とし、これにメッキ液を接触させるため
、メッキ液中に蓄積された夾雑物イオン、例えばNiイ
オンが下記に示すようにして捕捉除去される。なおこの
場合、処理液は上記の去応によりNi”1mon当り2
m0QのH゛が放出されpHが下がる傾向にあり、pH
維持のため、 NaOH等のアルカリを添加する必要が
ある。<Function> As described above, in the present invention, since the iminodiacetic acid-based chelate resin is made into H-type and the plating solution is brought into contact with it, the impurity ions accumulated in the plating solution, such as Ni ions, are It is captured and removed as shown. In this case, the treatment solution has a concentration of 2% per 1 mon of Ni due to the above-mentioned removal reaction.
H of m0Q is released and the pH tends to decrease, and the pH
For maintenance, it is necessary to add an alkali such as NaOH.
↓↑
また、 このようにしてNiイオンを捕捉したキレート
樹脂は酸により右側の矢印のように再生されることにな
る。↓↑ Also, the chelate resin that has captured Ni ions in this way is regenerated by acid as shown by the arrow on the right.
以下に実施例を示す。Examples are shown below.
実施例
粒径0.3〜1.2mのマクロポーラスタイプのイミノ
ジ酢酸基系樹脂35mj2RHを内径101mφのガラ
スカラムに充填し、下記組成および性状のZnメッキ液
を5V=8〜10hr”の流速で下向流で通液した。Example A macroporous type iminodiacetic acid-based resin 35mj2RH with a particle size of 0.3 to 1.2 m was packed into a glass column with an inner diameter of 101 mφ, and a Zn plating solution having the following composition and properties was applied at a flow rate of 5 V = 8 to 10 hr. The liquid was passed in a downward flow.
メッキ液
NaHz P 04 : 170g/ n ”
Ni : 232ppm
Zn : 532ppm
pH: 4.6
液温 :40〜50℃
この時の処理液中のNiイオン濃度の経時変化を第1図
の実線で示す。図より、処理液のN1リーク量は5 p
pm以下と良好であり、またNiの吸着量は40■Ni
/mQ−RHであった。一方、カラム内の樹脂35m
Q −RHをNaOHによりNa形にして上記メッキ液
を処理した時の処理液中のNiイオン濃度の経時変化を
第1図の破線で示す。Plating solution NaHz P 04: 170g/n”
Ni: 232 ppm Zn: 532 ppm pH: 4.6 Liquid temperature: 40 to 50°C The change over time in the Ni ion concentration in the treatment liquid at this time is shown by the solid line in FIG. From the figure, the amount of N1 leakage from the processing solution is 5 p.
It is good at less than pm, and the amount of Ni adsorbed is 40■Ni
/mQ-RH. On the other hand, 35 m of resin in the column
The broken line in FIG. 1 shows the change over time in the Ni ion concentration in the plating solution when Q-RH was converted into Na form with NaOH and treated with the above plating solution.
この場合、Niリーク量、吸着量ともにH形で使用した
時と同等であった、
く効 果〉
以上のような本発明は次のような効果を有する。In this case, both the amount of Ni leaked and the amount of Ni adsorbed were the same as when the H type was used. Effects> The present invention as described above has the following effects.
1)、イミノジ酢酸基系キレート樹脂をH形で使用でき
ることにより、酸による再生のみで使用でき、樹脂の再
生にNaOHを使用する必要がなくなるため、ランニン
グコストの低減がはかれる。1) Since the iminodiacetic acid group-based chelate resin can be used in the H form, it can be used only by regeneration with an acid, and there is no need to use NaOH for resin regeneration, so running costs can be reduced.
2)、また、キレート樹脂をH型で使用することにより
1通液、再生時の膨潤、収縮が少く、Na形で使った場
合に比べて樹脂の摩耗、破砕からくる劣化を最小限に抑
えることができる。2) Also, by using the chelate resin in the H type, there is less swelling and shrinkage during regeneration after one liquid pass, and compared to when using the Na type, deterioration caused by resin abrasion and crushing is minimized. be able to.
第1図は実施例におけるメッキ液の通液量とNiリーク
量との関係図である。
児 1 関
一−−−Na形使用
IL/L”Kl”IIFIG. 1 is a diagram showing the relationship between the amount of plating solution passed and the amount of Ni leakage in the example. Child 1 Sekiichi---Na type used IL/L"Kl"II
Claims (1)
樹脂で処理するに際し、このキレート樹脂をH形にして
メッキ液と接触させることを特徴とするメッキ液の処理
方法。 2、H形のキレート樹脂が硫酸で再生したものである特
許請求の範囲第1項記載のメッキ液の処理方法。[Scope of Claims] 1. A method for treating a plating solution, which is characterized in that when a plating solution is treated with a chelate resin having an iminodiacetic acid group as a functional group, the chelate resin is brought into H form and brought into contact with the plating solution. 2. The method for treating a plating solution according to claim 1, wherein the H-type chelate resin is regenerated with sulfuric acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19871186A JPS6357799A (en) | 1986-08-25 | 1986-08-25 | How to treat plating liquid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19871186A JPS6357799A (en) | 1986-08-25 | 1986-08-25 | How to treat plating liquid |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6357799A true JPS6357799A (en) | 1988-03-12 |
Family
ID=16395738
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19871186A Pending JPS6357799A (en) | 1986-08-25 | 1986-08-25 | How to treat plating liquid |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6357799A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5801319A (en) * | 1995-11-22 | 1998-09-01 | W.L. Gore & Associates, Inc. | Strings for musical instruments |
US5907113A (en) * | 1995-11-22 | 1999-05-25 | W. L. Gore & Associates, Inc. | Strings for musical instruments |
WO2002040405A3 (en) * | 2000-11-15 | 2002-07-25 | Henkel Kgaa | Treatment of nickel-containing waste water on phosphating |
US6765136B2 (en) | 2002-01-16 | 2004-07-20 | Gibson Guitar Corp. | Hydrophobic polymer string treatment |
US7217876B2 (en) | 2003-11-14 | 2007-05-15 | Gore Enterprise Holdings, Inc. | Strings for musical instruments |
WO2015014546A1 (en) * | 2013-07-31 | 2015-02-05 | Krones Ag | Method and device for material-oriented water treatment for mines |
-
1986
- 1986-08-25 JP JP19871186A patent/JPS6357799A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5801319A (en) * | 1995-11-22 | 1998-09-01 | W.L. Gore & Associates, Inc. | Strings for musical instruments |
US5883319A (en) * | 1995-11-22 | 1999-03-16 | W.L. Gore & Associates, Inc. | Strings for musical instruments |
US5907113A (en) * | 1995-11-22 | 1999-05-25 | W. L. Gore & Associates, Inc. | Strings for musical instruments |
US6248942B1 (en) | 1995-11-22 | 2001-06-19 | Gore Enterprise Holdings, Inc. | Strings for musical instruments |
WO2002040405A3 (en) * | 2000-11-15 | 2002-07-25 | Henkel Kgaa | Treatment of nickel-containing waste water on phosphating |
US6765136B2 (en) | 2002-01-16 | 2004-07-20 | Gibson Guitar Corp. | Hydrophobic polymer string treatment |
US7217876B2 (en) | 2003-11-14 | 2007-05-15 | Gore Enterprise Holdings, Inc. | Strings for musical instruments |
WO2015014546A1 (en) * | 2013-07-31 | 2015-02-05 | Krones Ag | Method and device for material-oriented water treatment for mines |
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