JPS6352093B2 - - Google Patents

Info

Publication number
JPS6352093B2
JPS6352093B2 JP3180982A JP3180982A JPS6352093B2 JP S6352093 B2 JPS6352093 B2 JP S6352093B2 JP 3180982 A JP3180982 A JP 3180982A JP 3180982 A JP3180982 A JP 3180982A JP S6352093 B2 JPS6352093 B2 JP S6352093B2
Authority
JP
Japan
Prior art keywords
silver
palladium
scrap
slag
precious metals
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
Application number
JP3180982A
Other languages
Japanese (ja)
Other versions
JPS58151434A (en
Inventor
Noboru Sakai
Eiichi Asada
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.)
Shoei Chemical Inc
Original Assignee
Shoei Chemical Inc
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 Shoei Chemical Inc filed Critical Shoei Chemical Inc
Priority to JP57031809A priority Critical patent/JPS58151434A/en
Publication of JPS58151434A publication Critical patent/JPS58151434A/en
Publication of JPS6352093B2 publication Critical patent/JPS6352093B2/ja
Granted 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

Description

【発明の詳細な説明】 本発明はパラジウムを含む磁器電子部品スクラ
ツプより、パラジウム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。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a method for easily separating and collecting palladium components in high yield from scrap of porcelain electronic parts containing palladium.

貴金属含有の鉱石またはスクラツプより貴金属
を分離採取する場合、鉱石またはスクラツプを鉛
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、直接強酸で溶解抽出して各貴金属
元素に分離する方法の二方法がある。
When separating precious metals from ores or scraps containing precious metals, the ore or scraps are melted together with lead and the precious metals are collected in the lead to form precious lead, which is then separated into each element by ash blowing and hydrometallurgy. There are two methods: one method is to separate each precious metal element by directly dissolving and extracting it with a strong acid.

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、さらに貴金属た
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が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
いろ問題があつた。後者は、貴金属を強酸で直接
溶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かりでなく、大
量の酸を用いるので危険を伴う。特に原料品位が
低い場合、不純物の溶出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。従つて浸出液と残渣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。
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. This method is not practical because some parts become chlorides and are lost by volatilization, and precious metals such as palladium and lead may interact to form poorly soluble intermetallic compounds, making subsequent acid treatment difficult. There were various problems. The latter method is superior at first glance, as it directly dissolves the precious metal with a strong acid to create a leachate and separates and purifies each element, but this requires a long time to separate the leachate and the residue, and is susceptible to contamination by impurities. Not only is separation difficult, but it is also dangerous because a large amount of acid is used. Particularly when the quality of the raw material is low, a large amount of impurities are eluted, making it difficult to separate the leachate, resulting in a large amount of processing time. Therefore, attempts have been made to simplify the separation of the leachate and residue by some means and 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 believed that solving the defects of the former method would have more advantages than the latter method, and as a result of various studies, we found that as long as lead was used, good results could not be obtained even if the processing conditions and additives were devised. They came to the conclusion that there was no such thing, and after further research considering the ease of subsequent separation, they developed a method to use silver to alloy silver and precious metals, and remove the gangue as slag.

本発明のパラジウムの採取方法は、電子部品ス
クラツプを、銀地金または銀の高含有スクラツプ
からなる銀供給材、およびケイ酸系造かん剤と混
合して溶融し、パラジウム成分を銀と合金化させ
て銀中に捕集し、貴金属以外の成分はスラグとし
て銀合金から分離させるものである。
The method for collecting palladium of the present invention involves mixing electronic component scrap with a silver supply material consisting of silver bullion or high-silver content scrap, and a silicic acid-based combustible agent, and melting the mixture to alloy the palladium component with silver. Components other than precious metals are separated from the silver alloy as slag.

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つて酸化除去する必
要がないこと、従つて有害な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。また強酸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. It has outstanding advantages such as no need for oxidation removal by the process and therefore no generation of harmful vapors or loss of precious metals. Also, compared to extraction methods using strong acids, there is less loss and contamination of impurities during the separation process.
It is also easy to operate.

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、後の精製処理を容易にする
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 and facilitate the subsequent refining process.

本発明において使用する銀供給材は、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
ツプ等を用いることができる。銀の量は捕集すべ
きパラジウム量の2倍以上を使用することが望ま
しい。
The silver supply material used in the present invention may be pure silver ingot, but scrap or the like with a relatively high silver content can be used. It is desirable to use at least twice the amount of silver as the amount of palladium to be collected.

造かん剤の添加は、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に、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、SiO2,Fe2O3,CaCO3,Na2CO3
Na2B4O7等の通常使用されるケイ酸系の溶剤成
分に、還元剤、酸化剤等が原料の鉱石、スクラツ
プの組成に応じて適宜配合される。組成は形成さ
れる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
0.5〜2.5、好ましくは0.8〜1.5程度になるように
調製する。
Addition of a flocculant is a common practice in the art in order to combine with components other than the target metal during melting and separate them as slag. As a flocculant, SiO 2 , Fe 2 O 3 , CaCO 3 , Na 2 CO 3 ,
A reducing agent, an oxidizing agent, etc. are appropriately blended with a commonly used silicic acid solvent component such as Na 2 B 4 O 7 depending on the composition of the raw material ore and scrap. The composition must be determined in advance so that the slag that is formed has a smooth, glass-like shape that is easily separated from the alloy part.
Practically speaking, the silicic acidity of the slag is calculated using the following formula:
It is adjusted to about 0.5 to 2.5, preferably about 0.8 to 1.5.

ケイ酸度=SiO2中の酸素の量/塩基性酸化物中の酸素
の量 鉱石、スクラツプおよび銀供給材は、造かん剤
と均一に混合できる程度に予め粉砕されているこ
とが望ましい。
Silicic acidity=Amount of oxygen in SiO 2 /Amount of oxygen in basic oxide It is desirable that the ore, scrap and silver feed material be pulverized in advance to the extent that they can be uniformly mixed with the flocculant.

溶融温度は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。
A suitable melting temperature is 1100°C or higher. At temperatures lower than this, the fluidity of the slag is insufficient.

本法によつて銀との合金として採取されたパラ
ジウムは、公知の精製法に従つて各成分金属に分
離精製される。
Palladium collected as an alloy with silver by this method is separated and purified into each component metal according to a known purification method.

次に本発明を実施例によつて説明する。 Next, the present invention will be explained with reference to examples.

各実施例において、予めスクラツプおよび銀供
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、Fe2O3はSiO2とともにスラグを形
成するためのものであり、Na2CO3,Na2B4O7
スラグをさらさら流れ易くするため、小麦粉は還
元雰囲気をつくつて有用金属の逸失を防止するた
め、またKNO3は共存する不要金属を酸化するた
めに添加した。
In each example, the scrap and silver supply materials were quantitatively analyzed in advance to determine the blending agent. Among the flocculant ingredients, Fe 2 O 3 is used to form slag with SiO 2 , and Na 2 CO 3 and Na 2 B 4 O 7 make the slag flow easily, so flour creates a reducing atmosphere. KNO 3 was added to prevent the loss of useful metals, and to oxidize coexisting unnecessary metals.

実施例 1 予め50メツシユ程度に粉砕したパラジウム10重
量%、白金2重量%を含むBaTiO3系磁器スクラ
ツプ2.5Kgと、銀供給材として90重量%銀含有ス
クラツプ5.0Kgおよび下記組成の造かん剤とを均
一に混合した。
Example 1 2.5 kg of BaTiO 3 -based porcelain scrap containing 10% by weight of palladium and 2% by weight of platinum that has been crushed into approximately 50 meshes in advance, 5.0 kg of scrap containing 90% by weight of silver as a silver supply material, and a pelletizer having the following composition. were mixed uniformly.

〔造かん剤〕 Fe2O3 0.7Kg SiO2 4.1Kg Na2CO3 6.5Kg Na2B4O7 2.3Kg 小麦粉 1.0Kg 混合物を素焼きのルツボに入れ、電気炉にて
1200℃に30分間保持し溶融した後、炉より取り出
し、円錘鋳型(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、合金部は下
層に、スラグは上層に分離されていた。
[Bottling agent] Fe 2 O 3 0.7Kg SiO 2 4.1Kg Na 2 CO 3 6.5Kg Na 2 B 4 O 7 2.3Kg Flour 1.0Kg The mixture was placed in an unglazed crucible and heated in an electric furnace.
After melting by holding at 1200°C for 30 minutes, it was taken out of the furnace and poured into a cone mold. When it was taken out from the mold after cooling, the alloy part 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、白金はすべて合金部に存在してお
り、また採取率約99%で、貴金属の逸失はほとん
どなかつた。
As a result of analyzing the alloy part and slag, silver,
Palladium and platinum were all present in the alloy, and the recovery rate was approximately 99%, with almost no loss of precious metals.

実施例 2 銀供給材として90重量%銀含有スクラツプを
2.5Kg、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と同様の処理を行つた。
Example 2 Using scrap containing 90% silver as a silver supply material
The same treatment as in Example 1 was carried out except that the weight was 2.5 kg and a flocculant having the following composition was used.

〔造かん剤〕 Fe2O3 2.5Kg SiO2 2.7Kg Na2CO3 4.3Kg Na2B4O7 1.4Kg 小麦粉 0.5Kg 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] Fe 2 O 3 2.5Kg SiO 2 2.7Kg Na 2 CO 3 4.3Kg Na 2 B 4 O 7 1.4Kg Flour 0.5Kg As a result, almost no precious metals were lost, and 99
% in high yield.

実施例 3 銀供給材として70重量%銀含有スクラツプを
2.5Kg、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と同様の処理を行つた。
Example 3 Scrap containing 70% silver as silver supply material
The same treatment as in Example 1 was carried out except that the weight was 2.5 kg and a flocculant having the following composition was used.

〔造かん剤〕 Fe2O3 2.5Kg SiO2 1.6Kg Na2CO3 2.7Kg Na2B4O7 2.3Kg KNO3 0.5Kg 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] Fe 2 O 3 2.5Kg SiO 2 1.6Kg Na 2 CO 3 2.7Kg Na 2 B 4 O 7 2.3Kg KNO 3 0.5Kg As a result, 99
% in high yield.

上記実施例はすべて磁器スクラツプからの採取
例であるが、鉱石や、他の貴金属含有スクラツプ
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 be similarly collected.

Claims (1)

【特許請求の範囲】[Claims] 1 パラジウム含有の磁器電子部品スクラツプ
と、銀地金または銀の高含有スクラツプからなる
銀供給材と、ケイ酸系造かん剤とを混合し溶融し
て、パラジウム成分を銀と合金化させて銀中に捕
集し、貴金属以外の成分はスラグとして分離する
ことによりパラジウムを採取する方法。
1 Mix and melt palladium-containing porcelain electronic component scrap, a silver supply material consisting of silver bullion or high-silver content scrap, and a silicic acid-based combustible agent to alloy the palladium component with silver to produce silver. A method of collecting palladium by collecting it in a slag and separating components other than precious metals as slag.
JP57031809A 1982-03-02 1982-03-02 Extracting method of noble metal Granted JPS58151434A (en)

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 JPS58151434A (en) 1983-09-08
JPS6352093B2 true 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 (1)

* Cited by examiner, † Cited by third party
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

Families Citing this family (2)

* Cited by examiner, † Cited by third party
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

Citations (2)

* Cited by examiner, † Cited by third party
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

Patent Citations (2)

* Cited by examiner, † Cited by third party
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 (1)

* Cited by examiner, † Cited by third party
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

Also Published As

Publication number Publication date
JPS58151434A (en) 1983-09-08

Similar Documents

Publication Publication Date Title
CA2933448C (en) A process for extracting noble metals from anode slime
US4135923A (en) Extraction of metals
US4427442A (en) Recovery of platinum group metals, gold and silver from scrap
US20120144959A1 (en) Smelting method
WO2021014946A1 (en) Pgm recovery method
JPS6352093B2 (en)
KR101817079B1 (en) process of recovering Platinum group metal from waste sludge generated from refining process of precious metal ore
JP2004270008A (en) Method for recovering noble metal
JP2587814B2 (en) Method for treating concentrate from copper converter
JPH04224639A (en) Method for purification of lead wherein copper is especially removed
JPS6221851B2 (en)
JPS61149445A (en) Method for recovering valuable metal from copper smelting slag
US2043575A (en) Process for detinning lead alloys
JPH101727A (en) Treatment of copper electrolyte slime
JP2019151863A (en) Method for recovering tin from copper smelting dust and recovered tin
JPS5929659B2 (en) Indium separation method
RU2432408C1 (en) Procedure for extraction of gold from rejects of electronic scrap
RU2153014C1 (en) Method of processing chloride slag containing noble metals
RU2221885C1 (en) Method of production of gold bullion alloy
RU2164256C2 (en) Method of processing alloys containing noble and nonferrous metals
RU2150521C1 (en) Method of processing chloride slag containing precious metals
RU2099435C1 (en) Pyrometallurgical method for recovering precious metals out of gravity concentrates
US370338A (en) Daeley c
JPS6049701B2 (en) Method for removing arsenic and/or copper in molten metal
RU2109829C1 (en) Charge for preparing precious metal alloy