JPS58151434A - Extracting method of noble metal - Google Patents
Extracting method of noble metalInfo
- Publication number
- JPS58151434A JPS58151434A JP57031809A JP3180982A JPS58151434A JP S58151434 A JPS58151434 A JP S58151434A JP 57031809 A JP57031809 A JP 57031809A JP 3180982 A JP3180982 A JP 3180982A JP S58151434 A JPS58151434 A JP S58151434A
- Authority
- JP
- Japan
- Prior art keywords
- silver
- noble metals
- scraps
- components
- slag
- 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
Landscapes
- Manufacture And Refinement Of Metals (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は貴金属、即ち白金族金属、金、銀を含む鉱石や
、電子部品、使用済み触媒等のスクラップより、貴金属
成分を高収率かつ容易に分離採取する方法を提供するも
のである0
貴金属含有の鉱石またはスクラップより貴金属を分離採
取する場合、鉱石またはスクラップを鉛とともに溶融し
貴金属を鉛の中に捕集して貴鉛となし、これを灰吹き、
湿式精錬により各元素に分離する方法と、直接強酸で溶
解抽田して各貴金属元素に分離する方法の二重性かめる
。[Detailed Description of the Invention] The present invention provides a method for easily separating and collecting precious metal components from precious metals, that is, ores containing platinum group metals, gold, and silver, scraps of electronic parts, used catalysts, etc., with high yield. 0 When separating and extracting precious metals from precious metal-containing ores or scraps, the ore or scraps are melted together with lead and the precious metals are collected in the lead to form precious lead.
The duality of the method of separating each element by hydrometallurgy and the method of separating each noble metal element by directly dissolving and extracting with a strong acid is highlighted.
しかし、前者は貴金属を捕集するために用いられた鉛が
灰吹きに際して酸化鉛となり揮発散するため公害の発生
源となること、この酸化鉛の揮発散を防ぐため食塩で被
覆すれば貴金属の一部分が塩化物となり揮発損失するこ
と、芒らにJj金金属とえばパラジウムと鉛とが作用し
て難溶性の金属間化合物を生成することかあり引続く酸
処理が困難となることなどから、この方法には実用上い
ろいろ問題があった。後者は、貴金属を強酸−〇直接浴
かし出して浸出液をつくり、各元素を分離精製するので
一見すぐれているが、これは浸出液と残渣との分離操作
に長時間を要し、かつ不純物が混入し易くその分離が困
難であるば刀・りでなく、大量の縁を用いるので危険を
伴う。特に原料品位が低い場合、不純物のIJlfll
も多く浸出液の分離が困難となり、処理に多大な時間を
費やすことになる。However, the former is a source of pollution because the lead used to collect precious metals becomes lead oxide and volatilizes during ash blowing, and if it is coated with common salt to prevent the lead oxide from volatilizing, precious metals can be removed. Some of the components become chlorides and are lost by volatilization, and gold metals such as palladium and lead may act on the awns to form poorly soluble intermetallic compounds, making subsequent acid treatment difficult. This method had many practical problems. The latter method is superior at first glance, as it creates a leachate by directly exposing the precious metal to a strong acid bath, and separates and purifies each element. If they easily get mixed up and it is difficult to separate them, a large amount of edges are used instead of swords and rigs, which is dangerous. Particularly when raw material quality is low, impurity IJlfll
This makes separation of the leachate difficult and requires a lot of time for treatment.
従って浸出液と残漬の分離操作を何らかの方法で単純化
し、所要時間を短くすることが試みられているが、満足
な結果は得られていない。Therefore, attempts have been made to simplify the separation operation between the leachate and the residue and to shorten the time required, but no satisfactory results have been obtained.
本発明者らは、後者の方法より前者の方法の有する欠陥
を解決すれば利点が多いと考えいろいろ研究した結果、
鉛を用いるかぎり処理条件や添加剤等を工夫しても良い
結果は得られないとの結論に達し、さらにその後の分離
の容易さも考慮して研究を重ね、銀を用いて銀と貴金属
とを合金化させ、脈石はスラグとして除去する方法を開
発した。The inventors of the present invention believe that solving the deficiencies of the former method has more advantages than the latter method, and have conducted various studies.
They came to the conclusion that as long as lead was used, good results could not be obtained no matter how different the processing conditions or additives were, and after further research taking into account the ease of subsequent separation, they succeeded in separating silver and precious metals using silver. We developed a method for alloying and removing gangue as slag.
本発明の貴金属の°採取方法は、鉱石またはスクラップ
を銀供給材および造かん剤と混合したものを溶融し、貴
金属成分を鎖中に捕集して、他成分はスラグとして銀合
金から分離させるものである。The method for collecting precious metals of the present invention involves melting ore or scrap mixed with a silver feed material and a flocculant, collecting precious metal components in chains, and separating other components from the silver alloy as slag. It is something.
この方法は鉛を用いて捕集する方法と比較して、難溶性
の合金を作ることがなく後に続く湿式処理が容易である
こと、銀は鉛を捕集剤として用いたときのように灰吹法
によって識化除去す。る必要がないこと、従って公害蒸
気の発生や貴金属の逸失が全くないことなど、極めてす
ぐれた利点を有する。また強ばで抽出する方法と比較し
ても、分離工程での損失や不純物の混入も少なく、操作
も簡単である。Compared to the method of collection using lead, this method does not create a poorly soluble alloy and the subsequent wet treatment is easy. De-identify by law. It has very good advantages, such as no need for water pollution, no generation of polluting vapors, and no loss of precious metals. Furthermore, compared to the method of extraction using strong barley, there is less loss and contamination of impurities during the separation process, and the operation is simple.
このように本発明は無公害、かつ貴金属採取率の高い精
製法であり、しかも手順と時間とを大幅に短縮するとと
もに、後の精製処理を容dにすることができたものであ
る。As described above, the present invention is a refining method that is non-polluting and has a high recovery rate of precious metals, and can significantly shorten the procedure and time, as well as simplify the subsequent refining process.
本発明において便用する銀供給材は、純銀地金でも差支
えないが、銀含有率の比較的高いスクラップ等を用いる
ことができる。銀の量は捕集すべき銀以外の貴金属量の
2倍以上を使用することが望ましい。The silver supply material conveniently used in the present invention may be pure silver bullion, but scrap or the like with a relatively high silver content can be used. It is desirable to use an amount of silver that is at least twice the amount of precious metals other than silver to be collected.
造かん剤の硼加は、溶融時に目的金属以外の成分と結合
させてスラグとして分離するためで、当業界で一般に行
なわれているものである。造かん剤としては、S i
Ow 1Fe203、CaC0a、Na2CO3、Na
2B4O7等の通常使用される溶剤成分に、還元たす、
酸化剤等が原料の鉱石、スクラップの組成に応じて適宜
配合される。組成はスラグが合金部と分離し易い、さら
さらしたガラス状となるよう予め決めておく必要がある
。実用的には次式で算出されるスラグのケイ酸度が0.
5〜25、好ましくはo、8〜1.5@度になるように
調製する。Boronization of the flocculant is commonly carried out in the industry to combine components other than the target metal during melting and separate them as slag. As a flocculant, S i
Ow 1Fe203, CaC0a, Na2CO3, Na
Reduction to commonly used solvent components such as 2B4O7,
Oxidizing agents and the like are appropriately blended depending on the composition of the raw material ore and scrap. The composition must be determined in advance so that the slag has a smooth, glass-like appearance that is easily separated from the alloy part. Practically speaking, the silicic acidity of the slag calculated by the following formula is 0.
The temperature is adjusted to 5 to 25 degrees, preferably 8 to 1.5 degrees.
5102中の酸素の菫
ケイ酸度=−一−−−一−−−−−−−−−塩基性酸化
物中の酸素の量
鉱石、スクラップおよび銀供給材は、造力・ん剤と均一
に混合でさる程度に予め粉砕されていることが望ましい
。Lissilicic acidity of oxygen in 5102 = -1 - - -1 - - Amount of oxygen in basic oxide Ore, scrap and silver feed materials are uniformly mixed with the forming agent and powder. It is preferable that the powder be crushed in advance to a sufficient degree during mixing.
溶曽温度lは1100℃以上が適当である。これより低
い温度では、スラグの流動性が充分でない。The melting temperature l is suitably 1100°C or higher. At temperatures lower than this, the fluidity of the slag is insufficient.
拳法によって銀との合金として採取された貴金属は、公
知の精製法に従って各成分金属に分離精製される。Precious metals collected as alloys with silver by Kenpo are separated and refined into each component metal according to known refining methods.
次に本発明を実施例によって説明する。Next, the present invention will be explained by examples.
各実施例において、予めスクラップおよび銀供給材を定
量分析し、造かん剤の配合を決めた。造かん剤成分中、
Fe、0.はSiO□とともにスラグを形成するための
ものであり、Na2C!O,、Na、 B、 07はス
ラグをさらさら流れ易くするため、小麦粉は還元雰囲気
として有用金員の逸失を防止するため、またKNO3は
共存する不委金属を酸化するために添加した。In each example, scrap and silver feed materials were quantitatively analyzed in advance to determine the blending agent. Among the flocculant ingredients,
Fe, 0. is for forming slag with SiO□, and Na2C! O, Na, B, 07 were added to make the slag flow easily, wheat flour was added to create a reducing atmosphere to prevent the loss of useful metals, and KNO3 was added to oxidize coexisting undesirable metals.
実施例1゜
予め50メツシュ程度に粉砕したパラジウム10重量%
、白金2重量%を含むBaTiOs系磁器スクラップ2
.5 hと、銀供給材として90重量c6銀含有スクラ
ップ50に7および下記組成の造かん剤とを均一に混合
した。Example 1゜10% by weight of palladium pre-pulverized to about 50 meshes
, BaTiOs-based porcelain scrap 2 containing 2% by weight of platinum
.. 5 h and 90 weight c6 silver-containing scrap 50 as a silver supply material were uniformly mixed with 7 and a granulating agent having the following composition.
〔造かん剤] Fe2O,0,7KりSi0□
41寸
Na2Co36.5 h9
Na2B、 0. 2ろhq
小麦粉 10に?
混合物を素焼きのルツボに入れ、電気炉にて1200℃
に60分間保持し浴融した後、炉より取り出し、円錐鋳
型(コーンモールド)に流し、込み、冷却後モールドよ
り取り出したところ、付金部は下層に、スラグは上層に
分離されていた。[Bottling agent] Fe2O, 0.7K, Si0□
41 inch Na2Co36.5 h9 Na2B, 0. 2 hq flour to 10? The mixture was placed in an unglazed crucible and heated to 1200℃ in an electric furnace.
After being melted in the bath for 60 minutes, it was taken out from the furnace, poured into a cone mold, poured into a cone mold, cooled, and taken out from the mold. When it was taken out from the mold, the ferrule was separated into the lower layer and the slag was separated into the upper layer.
合金部、スラグをそれぞれ分析した結果、銀、パラジウ
ム、白午(rゴ丁べて合金部に存狂し1おり、また採取
率約99%で、責金媚の逸失はほとんどなかった。As a result of analyzing the alloy part and slag, it was found that silver, palladium, and white gold were present in the alloy part, and the collection rate was about 99%, and there was almost no loss of silver.
実施例2゜
峠供給材として90重量%銀含有スクラップを2、5
K9 、造かん剤として下記組成のものを用いる以外は
実施例1.と同様の処理を行った。Example 2 Two to five scraps containing 90% by weight silver were used as a pass feed material.
K9, Example 1 except that the flocculant having the following composition was used. The same process was performed.
〔造かん剤) Fe2O,2,5KgSin22.
7 Kg
Na2 co、 4.3 Kr
Na213. O? 1.4 Kg
小麦粉 0.5 Kg
結果は貴金属をほとんど逸失することなく、99%の高
収率で採取できた。[Bottling agent] Fe2O, 2,5KgSin22.
7 Kg Na2 co, 4.3 Kr Na213. O? 1.4 Kg Flour 0.5 Kg As a result, precious metals were collected at a high yield of 99% with almost no loss.
実施例ろ
銀供給材として一秒港70重量%銀含有スクラップを2
.5Ky、造かん剤と1.て下記組成のものを用いる以
外は実施例1.と同様の処理を行った。Example filtration 70% by weight silver-containing scrap was used as a silver supply material.
.. 5Ky, flocculant and 1. Example 1 except that the following composition was used. The same process was performed.
〔造かん剤) Fe2O32,5Kr51o、
1.6 Ks+
Na2 Co、 2.71=y
N、a2 B、o−t 2.3 ’1qK
N0. 0.5 Kp
結果は貴金属をほとんど逸失することなく、99%の高
収率で採取できた。[Bottling agent] Fe2O32,5Kr51o,
1.6 Ks+ Na2 Co, 2.71=y N, a2 B, o-t 2.3 '1qK
N0. 0.5 Kp As a result, precious metals were collected at a high yield of 99% with almost no loss.
上記実施例はすべて磁器スクラップからの採取例である
が、鉱石や、他の貴金属含有スクラップにおいても同様
に採取できることは言うまでもない。Although the above embodiments are all examples of collection from porcelain scrap, it goes without saying that ore and other precious metal-containing scraps can also be collected in the same way.
時計出願人 昭栄化学工業株式会社Watch applicant Shoei Chemical Industry Co., Ltd.
Claims (1)
、造かん剤とを混合し溶融して、貴金属成分を鎖中に捕
集し、卑金属成分はスラグとして分離することにより貴
金属を採取する方法01 A method for extracting precious metals by mixing and melting precious metal-containing ore or scrap, silver supply material, and a flocculant, collecting the precious metal components in chains, and separating the base metal components as slag 0
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57031809A JPS58151434A (en) | 1982-03-02 | 1982-03-02 | Extracting method of noble metal |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57031809A JPS58151434A (en) | 1982-03-02 | 1982-03-02 | Extracting method of noble metal |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58151434A true JPS58151434A (en) | 1983-09-08 |
JPS6352093B2 JPS6352093B2 (en) | 1988-10-18 |
Family
ID=12341416
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57031809A Granted JPS58151434A (en) | 1982-03-02 | 1982-03-02 | Extracting method of noble metal |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58151434A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6311626A (en) * | 1986-06-30 | 1988-01-19 | Nippon Mining Co Ltd | Method for recovering valuable metal |
CN1039136C (en) * | 1995-05-24 | 1998-07-15 | 昆明贵金属研究所 | Enriching and activating and dissolving method for low grade and difficult treating noble metal materials |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03217790A (en) * | 1990-01-22 | 1991-09-25 | Japan Drive-It Co Ltd | Lining material supporting structure for wall surface |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5337523A (en) * | 1976-09-20 | 1978-04-06 | Nippon Mining Co Ltd | Refining of copper electrolytic slime |
JPS568897A (en) * | 1979-06-12 | 1981-01-29 | Telettra Lab Telefon | Universal rack for containing communication equipment |
-
1982
- 1982-03-02 JP JP57031809A patent/JPS58151434A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5337523A (en) * | 1976-09-20 | 1978-04-06 | Nippon Mining Co Ltd | Refining of copper electrolytic slime |
JPS568897A (en) * | 1979-06-12 | 1981-01-29 | Telettra Lab Telefon | Universal rack for containing communication equipment |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6311626A (en) * | 1986-06-30 | 1988-01-19 | Nippon Mining Co Ltd | Method for recovering valuable metal |
JPH0236652B2 (en) * | 1986-06-30 | 1990-08-20 | Nippon Mining Co | |
CN1039136C (en) * | 1995-05-24 | 1998-07-15 | 昆明贵金属研究所 | Enriching and activating and dissolving method for low grade and difficult treating noble metal materials |
Also Published As
Publication number | Publication date |
---|---|
JPS6352093B2 (en) | 1988-10-18 |
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