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JP3162294B2 - Back extraction method for palladium and back extraction method for platinum - Google Patents
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JP3162294B2 - Back extraction method for palladium and back extraction method for platinum - Google Patents

Back extraction method for palladium and back extraction method for platinum

Info

Publication number
JP3162294B2
JP3162294B2 JP17081596A JP17081596A JP3162294B2 JP 3162294 B2 JP3162294 B2 JP 3162294B2 JP 17081596 A JP17081596 A JP 17081596A JP 17081596 A JP17081596 A JP 17081596A JP 3162294 B2 JP3162294 B2 JP 3162294B2
Authority
JP
Japan
Prior art keywords
palladium
platinum
extracted
aqueous phase
back extraction
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.)
Expired - Fee Related
Application number
JP17081596A
Other languages
Japanese (ja)
Other versions
JPH1017952A (en
Inventor
勝利 井上
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.)
Tanaka Kikinzoku Kogyo KK
Original Assignee
Tanaka Kikinzoku Kogyo KK
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 Tanaka Kikinzoku Kogyo KK filed Critical Tanaka Kikinzoku Kogyo KK
Priority to JP17081596A priority Critical patent/JP3162294B2/en
Publication of JPH1017952A publication Critical patent/JPH1017952A/en
Application granted granted Critical
Publication of JP3162294B2 publication Critical patent/JP3162294B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

  • Manufacture And Refinement Of Metals (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は白金とパラジウムの
回収、精製時に用いられる、これら両金属の抽出剤に抽
出された白金とパラジウムを効率良く逆抽出することが
できる、白金とパラジウムの逆抽出方法に関するもので
ある。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for back-extraction of platinum and palladium, which can be used for the recovery and purification of platinum and palladium. It is about the method.

【0002】[0002]

【従来の技術】従来白金やパラジウムをはじめとする貴
金属の回収精製法には種々のものがあり、王水などの酸
に溶解して還元剤を加えて貴金属を選択的に還元し、濾
過分離するという化学還元法などが用いられてきた。近
年、溶媒抽出法やイオン交換法による回収精製法も開発
されてきたが、白金とパラジウムの分離はそれらの方法
を用いても容易ではない。例えば、高分子量アミンや陰
イオン交換樹脂を用いればこれらの金属は塩酸中から強
力に抽出されるが、両者の相互分離が困難な上、逆抽出
が困難であり、抽出溶媒や樹脂を焼却して回収すること
も行われている。またINCO社のACTON製錬所で
はパラジウムをジオクチルスルフィードを用いて抽出し
た後、TBPを用いて白金を回収するという分離・回収
法も提案されているが、この場合硫黄化合物であるジオ
クチルスルフィードには使用中に空気中の酸素により酸
化され抽出容量とパラジウムに対する選択性が低下する
という欠点がある。さらにパラジウムをヒドロキシオキ
シムで抽出して回収した後、高分子量アミンでパラジウ
ムを逆抽出して回収するという方法もあるが、このプロ
セスに用いられるヒドロキシオキシムも使用中に空気中
の酸素により酸化され、抽出容量が低下するという欠点
がある上、逆抽出が容量でない。
2. Description of the Related Art There are various methods for recovering and refining precious metals such as platinum and palladium, which are dissolved in an acid such as aqua regia and added with a reducing agent to selectively reduce the precious metals. For example, a chemical reduction method has been used. In recent years, recovery and purification methods by a solvent extraction method and an ion exchange method have been developed, but separation of platinum and palladium is not easy even by using these methods. For example, if a high molecular weight amine or anion exchange resin is used, these metals are strongly extracted from hydrochloric acid, but the two are difficult to separate from each other and difficult to back-extract, and the extraction solvent and resin are incinerated. They are also being collected. The ACCO smelter of INCO also proposes a separation / recovery method in which palladium is extracted using dioctyl sulfide and platinum is recovered using TBP. In this case, dioctyl sulfode which is a sulfur compound is used. Has the drawback that during use it is oxidized by oxygen in the air, reducing the extraction capacity and selectivity for palladium. Furthermore, after extracting and recovering palladium with hydroxyoxime, there is a method in which palladium is back-extracted and recovered with a high molecular weight amine, but the hydroxyoxime used in this process is also oxidized by oxygen in the air during use, In addition to the drawback that the extraction capacity is reduced, back extraction is not a capacity.

【0003】このような従来技術を解決するものとし
て、本発明者らは化1で表される貴金属、特に白金とパ
ラジウムの抽出剤及び貴金属の分離方法を発明した(特
開平7−62462号)。この抽出剤は白金、パラジウ
ムを効率良く抽出することが可能で、さらに条件を選択
することにより、白金とパラジウムをそれぞれ分別して
抽出することが可能であった。このように化1で表され
る抽出剤は効率の良いものであったが、回収された白
金、パラジウムは有機溶媒相に存在し。その後の回収操
作をより容易にするために、回収された白金、パラジウ
ムをさらに水相中へ逆抽出する、逆抽出方法の出現が望
まれていた。
In order to solve such a prior art, the present inventors have invented a noble metal represented by Chemical formula 1, especially an extractant for platinum and palladium, and a method for separating noble metals (Japanese Patent Laid-Open No. 7-62462). . This extractant was able to efficiently extract platinum and palladium, and further, by selecting conditions, it was possible to separate and extract platinum and palladium. Thus, the extractant represented by Chemical Formula 1 was efficient, but the recovered platinum and palladium existed in the organic solvent phase. In order to make the subsequent recovery operation easier, it has been desired to develop a back extraction method in which the recovered platinum and palladium are further back-extracted into an aqueous phase.

【0004】[0004]

【発明が解決しようとする課題】本発明は上記課題を解
決し、化1で表される抽出剤に抽出された白金、パラジ
ウムを効率よく逆抽出する方法を提供することを目的と
する。
An object of the present invention is to solve the above-mentioned problems and to provide a method for efficiently back-extracting platinum and palladium extracted by the extractant represented by Chemical formula 1.

【0005】[0005]

【課題を解決するための手段】本発明の白金の逆抽出方
法は、白金を抽出した化1で表される抽出剤を含む有機
相と、飽和濃度の亜二チオン酸塩の水相とを接触させ、
水相中へ白金を移動させることを特徴とする。
Back extraction method for platinum SUMMARY OF THE INVENTION The present invention provides an organic phase containing the extraction agent represented by the extracted of 1 platinum, an aqueous phase of the dithionite salt saturation concentration Contact,
It is characterized by moving platinum into the aqueous phase.

【0006】さらに本発明のパラジウムの逆抽出方法
は、パラジウムを抽出した化1で表される抽出剤を含む
有機相と、飽和濃度の亜二チオン酸塩の水相とを接触さ
せ、水相中へパラジウムを移動させることを特徴とする
ものである。
Further, according to the method for back extraction of palladium of the present invention, an organic phase containing an extracting agent represented by Chemical formula 1 in which palladium is extracted is brought into contact with an aqueous phase of a dithionite salt at a saturated concentration. It is characterized in that palladium is moved in.

【0007】[0007]

【発明の実施の形態】以下に本発明の実施の形態を示す
が、本発明は以下の例に限定されるものではない。
Embodiments of the present invention will be described below, but the present invention is not limited to the following examples.

【0008】[0008]

【実施例1】化1で表される白金の抽出剤の一例として
ジ(2−エチルヘキシル)シアミナドを用いた。白金を
73ppm含む0.1Mのジ(2−エチルヘキシル)シアミ
ナドのトルエン溶液と飽和濃度の亜ニチオン酸ナトリウ
ムの水溶液とをO/A比(油相と水相の体積比)が1:
1で24時間振り混ぜたところ、白金は表1ように水相
中へ逆抽出された。
Example 1 Di (2-ethylhexyl) cyanamine was used as an example of the platinum extractant represented by Chemical formula 1. Platinum
73ppm containing 0.1M di (2-ethylhexyl) Shiaminado an aqueous solution of sodium dithionite O / A ratio of a toluene solution and saturated concentration (volume ratio of oil and water phases) is 1:
After shaking for 24 hours, the platinum was back-extracted into the aqueous phase as shown in Table 1.

【0009】[0009]

【表1】 [Table 1]

【0010】[0010]

【実施例2】化1で表されるパラジウムの抽出剤の一例
としてジ(2−エチルヘキシル)シアミナドを用いた。
パラジウムを95ppm含む0.1Mのジ(2−エチルヘキ
シル)シアミナドのトルエン溶液と飽和濃度の亜二チオ
ン酸ナトリウムの水溶液とをO/A比(油相と水相の体
積比)が1:1で24時間振り混ぜたところ、パラジウム
は表2のように水相中へ逆抽出された。
Example 2 Di (2-ethylhexyl) cyanamid was used as an example of the palladium extractant represented by Chemical formula 1.
And an aqueous solution of sodium dithionite O / A ratio of a toluene solution and saturated concentration of palladium in 0.1M containing 95ppm di (2-ethylhexyl) Shiaminado (volume ratio of oil and water phases) is 1: 1 After shaking for 24 hours, palladium was back-extracted into the aqueous phase as shown in Table 2.

【0011】[0011]

【表2】 [Table 2]

【0012】[0012]

【発明の効果】以上のとおり、本発明の白金の逆抽出方
法及びパラジウムの逆抽出方法によれば、化1で表され
る抽出剤に抽出された白金及びパラジウムを高効率で逆
抽出することができ、その後の回収操作を容易にするも
のである。
As described above, according to the method for back extraction of platinum and the method for back extraction of palladium of the present invention, the platinum and palladium extracted by the extractant represented by Chemical Formula 1 can be back-extracted with high efficiency. To facilitate the subsequent recovery operation.

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 一般式 【化1】 (ここでR1、R2は炭素数6以上のアルキル基である)
で表される白金の抽出剤に抽出された白金を逆抽出する
方法において、上記白金を抽出した白金の抽出剤を含む
有機相と、飽和濃度の亜二チオン酸塩の水相とを接触さ
せ、水相中へ白金を移動させることを特徴とする白金の
逆抽出方法。
1. A compound of the general formula (Where R 1 and R 2 are alkyl groups having 6 or more carbon atoms)
A method for stripping platinum is extracted in the extracting agent of the platinum represented, is contacted with an organic phase comprising the extracting agent of platinum extracted the platinum, and the aqueous phase dithionite salt saturation concentration And back-extracting platinum into the aqueous phase.
【請求項2】 一般式 【化2】 (ここでR1、R2は炭素数6以上のアルキル基である)
で表されるパラジウムの抽出剤に吸着したパラジウムを
逆抽出する方法において、上記パラジウムを抽出したパ
ラジウムの抽出剤を含む有機相と、飽和濃度の亜二チオ
ン酸塩の水相とを接触させ、水相中へパラジウムを移動
させることを特徴とするパラジウムの逆抽出方法。
2. A compound of the general formula (Where R 1 and R 2 are alkyl groups having 6 or more carbon atoms)
In the method of back-extracting palladium adsorbed on the palladium extractant represented by, the organic phase containing the palladium extractant from which the palladium has been extracted is brought into contact with an aqueous phase of a dithionite salt at a saturated concentration, A method for back-extraction of palladium, comprising moving palladium into an aqueous phase.
JP17081596A 1996-07-01 1996-07-01 Back extraction method for palladium and back extraction method for platinum Expired - Fee Related JP3162294B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17081596A JP3162294B2 (en) 1996-07-01 1996-07-01 Back extraction method for palladium and back extraction method for platinum

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17081596A JP3162294B2 (en) 1996-07-01 1996-07-01 Back extraction method for palladium and back extraction method for platinum

Publications (2)

Publication Number Publication Date
JPH1017952A JPH1017952A (en) 1998-01-20
JP3162294B2 true JP3162294B2 (en) 2001-04-25

Family

ID=15911854

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17081596A Expired - Fee Related JP3162294B2 (en) 1996-07-01 1996-07-01 Back extraction method for palladium and back extraction method for platinum

Country Status (1)

Country Link
JP (1) JP3162294B2 (en)

Also Published As

Publication number Publication date
JPH1017952A (en) 1998-01-20

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