Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPH0753892B2 - Metal melting method - Google Patents
[go: Go Back, main page]

JPH0753892B2 - Metal melting method - Google Patents

Metal melting method

Info

Publication number
JPH0753892B2
JPH0753892B2 JP2124543A JP12454390A JPH0753892B2 JP H0753892 B2 JPH0753892 B2 JP H0753892B2 JP 2124543 A JP2124543 A JP 2124543A JP 12454390 A JP12454390 A JP 12454390A JP H0753892 B2 JPH0753892 B2 JP H0753892B2
Authority
JP
Japan
Prior art keywords
metal
dissolved
mmol
added
halogen
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 - Lifetime
Application number
JP2124543A
Other languages
Japanese (ja)
Other versions
JPH0421726A (en
Inventor
幸道 中尾
享二 帰山
愛造 山内
Original Assignee
工業技術院長
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 工業技術院長 filed Critical 工業技術院長
Priority to JP2124543A priority Critical patent/JPH0753892B2/en
Publication of JPH0421726A publication Critical patent/JPH0421726A/en
Publication of JPH0753892B2 publication Critical patent/JPH0753892B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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】 〔産業上の利用分野〕 本発明は、金属の溶解方法に関するものであり、詳しく
は、可溶性ハロゲン化塩の存在下にハロゲン及び極性溶
媒に接触させることを特徴とする金属の溶解方法に関す
るものである。
TECHNICAL FIELD The present invention relates to a method for dissolving a metal, which is characterized in that it is contacted with a halogen and a polar solvent in the presence of a soluble halide salt. The present invention relates to a method for melting a metal.

〔従来の技術〕[Conventional technology]

金属を液体中に溶解することは、金属を含有する混合物
から金属を抽出、回収するために不可欠の工程であり、
産業上極めて重要である。この目的のため、従来は、金
属を塩酸などの無機酸の水溶液に溶解する方法がとられ
ていた。
Dissolving a metal in a liquid is an essential step for extracting and recovering the metal from a mixture containing the metal,
It is extremely important in industry. For this purpose, conventionally, a method of dissolving a metal in an aqueous solution of an inorganic acid such as hydrochloric acid has been used.

また最近、陽イオン性界面活性剤の存在下にハロゲン化
炭化水素に接触させることにより金属を溶解させる方法
が見出されている(特開平1−294830号公報)。
Recently, a method of dissolving a metal by contacting it with a halogenated hydrocarbon in the presence of a cationic surfactant has been found (JP-A-1-294830).

〔発明が解決しようとする課題〕[Problems to be Solved by the Invention]

従来の無機酸を用いる金属の溶解方法では、強酸性の水
溶液を扱うため、作業が危険となるうえ、多量の酸性排
水が生じ、この排水の処理に多大の経費がかかる。ま
た、陽イオン性界面活性剤の存在下にハロゲン化炭化水
素に接触させる方法は、溶媒がハロゲン化炭化水素に限
られるうえ、その臭気や毒性が強いため作業に困難を伴
うなどの問題点があった。
In the conventional metal dissolution method using an inorganic acid, since a strongly acidic aqueous solution is used, the work is dangerous and a large amount of acidic waste water is generated, and the waste water is expensive to treat. In addition, the method of contacting with a halogenated hydrocarbon in the presence of a cationic surfactant has a problem in that the solvent is limited to the halogenated hydrocarbon, and that its odor and toxicity are strong, which makes work difficult. there were.

〔課題を解決するための手段〕[Means for Solving the Problems]

本発明者は、こうした従来の方法の課題を解決するた
め、無機酸を用いず、ハロゲン化炭化水素以外の有機溶
媒をも用い得る金属の溶解方法を求めて種々検討した結
果、多くの金属が、可溶性ハロゲン化塩、ハロゲン単体
及び極性溶媒に接触させることにより容易に溶解する現
象を見出し、本発明に到達した。
In order to solve the problems of the conventional methods, the present inventor has variously studied for a dissolution method of a metal that does not use an inorganic acid and can also use an organic solvent other than a halogenated hydrocarbon, and as a result, many metals are found to be present. The present invention has been accomplished by finding a phenomenon that it is easily dissolved by contact with a soluble halogenated salt, a simple substance of halogen, and a polar solvent.

すなわち、本発明は、可溶性ハロゲン化塩、ハロゲン単
体及び極性溶媒に接触させることを特徴とする金属の溶
解方法を提供するものである。
That is, the present invention provides a method for dissolving a metal, which comprises contacting with a soluble halide salt, a simple substance of halogen, and a polar solvent.

本発明方法においては、可溶性ハロゲン化塩、ハロゲン
単体及び極性溶媒に金属を接触させることにより金属を
溶解しやすい化合物に変換する。
In the method of the present invention, a metal is converted into a compound in which the metal is easily dissolved by bringing the metal into contact with a soluble halogenated salt, a simple substance of halogen and a polar solvent.

すなわち、目的の金属に対し、ハロゲンからハロゲン原
子が与えられることによって金属ハロゲン化物が生成
し、これが可溶性ハロゲン化塩の働きで溶解性の高いポ
リハロゲノ金属陰イオン錯体に変換されて極性溶媒に溶
解するわけである。
That is, when a halogen atom is given from a halogen to a target metal, a metal halide is generated, which is converted into a highly soluble polyhalogeno metal anion complex by the action of a soluble halide salt and is dissolved in a polar solvent. That is why.

金属の溶解に要する時間は、目的とする金属、用いる可
溶性ハロゲン化塩及びハロゲン単体の種類及び濃度、極
性溶媒の種類などにより異る。処理温度は極性溶媒の沸
点以下の範囲で選ばれるが、この処理温度が高いほど金
属の溶解が促進される。金属の溶解の終点は、仕込んだ
金属が見えなくなることで容易に確認できる。
The time required to dissolve the metal differs depending on the target metal, the type and concentration of the soluble halide salt and halogen simple substance used, the type of polar solvent, and the like. The treatment temperature is selected within a range not higher than the boiling point of the polar solvent, and the higher the treatment temperature, the more accelerated the dissolution of the metal. The end point of melting of the metal can be easily confirmed when the charged metal disappears.

本発明方法において用いられる可溶性ハロゲン化塩とし
ては、構成する陽イオンが、アルカリ金属イオン、アル
カリ土類金属イオンまたは一般式 (式中、R1、R2、R3及びR4は水素原子または炭素数6以
下の炭化水素基)で表わされるイオンであり、陰イオン
が、塩素イオン、臭素イオンまたはヨウ素イオンである
塩が適し、例えば、ヨウ化ナトリウム、臭化カリウム、
臭化カルシウム、臭化アンモニウム、メチルアミン塩酸
塩、ヨウ化テトラメチルアンモニウムなどが用いられ
る。可溶性ハロゲン化塩は、溶解すべき金属に対して等
モル以上、ハロゲン単体は、溶解すべき金属に対して0.
5倍モル量以上使用しなければならない。
As the soluble halogenated salt used in the method of the present invention, the constituent cations are alkali metal ions, alkaline earth metal ions or general formulas. (Wherein R 1 , R 2 , R 3 and R 4 are hydrogen atoms or hydrocarbon groups having 6 or less carbon atoms) and the anion is a chloride ion, a bromide ion or an iodide ion Are suitable, for example sodium iodide, potassium bromide,
Calcium bromide, ammonium bromide, methylamine hydrochloride, tetramethylammonium iodide and the like are used. Soluble halide salt is equimolar or more to the metal to be dissolved, simple halogen is 0 to the metal to be dissolved.
Must use more than 5 times the molar amount.

本発明方法で、ハロゲン単体としては、塩素、臭素及び
ヨウ素が用いられる。
In the method of the present invention, chlorine, bromine and iodine are used as the simple substance of halogen.

本発明方法では、極性溶媒として、水または液状の極性
有機溶媒、及びこれらの混合物が用いられる。液状の極
性有機溶媒としては、アルコール類、ケトン類、ニトリ
ル類が適し、例えば、メタノール、エタノール、アセト
ン、アセトニトリルが用いられる。
In the method of the present invention, water or a liquid polar organic solvent and a mixture thereof are used as the polar solvent. As the liquid polar organic solvent, alcohols, ketones and nitriles are suitable, and for example, methanol, ethanol, acetone and acetonitrile are used.

本発明方法により溶解される金属は、典型金属及び遷移
金属の両方にわたり、たとえば、ベリリウム、マグネシ
ウム、アルミニウム、チタン、バナジウム、クロム、マ
ンガン、鉄、コバルト、ニッケル、銅、亜鉛、セレン、
ジルコニウム、ニオブ、モリブデン、パラジウム、銀、
インジウム、錫、アンチモン、テルル、ハフニウム、タ
ンタル、金、水銀、鉛、ビスマスなどである。
The metals dissolved by the method of the present invention include both typical metals and transition metals, such as beryllium, magnesium, aluminum, titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, zinc, selenium,
Zirconium, niobium, molybdenum, palladium, silver,
Examples include indium, tin, antimony, tellurium, hafnium, tantalum, gold, mercury, lead and bismuth.

〔実施例〕〔Example〕

次に、実施例により、本発明を詳細に説明する。 Next, the present invention will be described in detail with reference to examples.

実施例 1〜23 メタノール10gに、臭化カリウム1mmol及び臭素0.5mmol
を溶解し、さらに表1に示す金属粉末0.2mg−atomを加
え、液温20℃で撹拌した。ここで、金属の粉末が全て溶
解し残存していない場合には溶解率100%とし、金属残
査がある場合には、これを傾しゃにより溶液から分離
し、メタノールで洗浄し乾燥した後秤量した。こうして
得た金属残査量と仕込量との差から金属の溶解率を求め
た。結果は表1の通りである。
Examples 1 to 23 To 10 g of methanol, 1 mmol of potassium bromide and 0.5 mmol of bromine
Was dissolved, 0.2 mg-atom of metal powder shown in Table 1 was added, and the mixture was stirred at a liquid temperature of 20 ° C. Here, if all the metal powder is dissolved and does not remain, the dissolution rate is set to 100%, and if there is a metal residue, it is separated from the solution by decanting, washed with methanol, dried, and then weighed. did. The dissolution rate of the metal was obtained from the difference between the amount of the residual metal thus obtained and the amount of the charged metal. The results are shown in Table 1.

実施例24〜26 アセトン10gに、ヨウ化ナトリウム1mmol及びヨウ素0.5m
molを加えて溶解し、さらに表2に示す金属粉末0.2mg−
atomを加え、液温56℃で撹拌しながら還流加熱したとこ
ろ、金属粉末はすべて溶解した。
Examples 24-26 To 10 g of acetone, 1 mmol of sodium iodide and 0.5 m of iodine
0.2 mg- of metal powder shown in Table 2
When atom was added and the mixture was heated under reflux at a liquid temperature of 56 ° C. with stirring, all the metal powder was dissolved.

実施例27 アセトニトリル10gに、ヨウ化ナトリウム1mmol及びヨウ
素0.5mmolを加えて溶解し、さらに0.2mmφの線状の金0.
2mg−atomを加え、液温82℃で撹拌しながら8時間還流
加熱したところ、線状の金はすべて溶解した。
Example 27 To 10 g of acetonitrile, 1 mmol of sodium iodide and 0.5 mmol of iodine were added and dissolved, and 0.2 mmφ linear gold was added.
When 2 mg-atom was added and the mixture was heated under reflux at a liquid temperature of 82 ° C. for 8 hours with stirring, all the linear gold was dissolved.

実施例28 メタノール10gに、臭化カルシウム1mmol及び臭素0.5mmo
lを加えて溶解し、さらに0.2mmφの線状の金0.2mg−ato
mを加え、液温20℃で8時間撹拌したところ、線状の金
はすべて溶解した。
Example 28 To 10 g of methanol, 1 mmol of calcium bromide and 0.5 mmo of bromine
l was added and dissolved, and 0.2 mmφ linear gold 0.2 mg-ato
When m was added and the mixture was stirred at a liquid temperature of 20 ° C. for 8 hours, all the linear gold was dissolved.

実施例29 水10gに、臭化アンモニウム1mmol及び臭素0.5mmolを加
えて溶解し、さらに0.2mmφの線状の金0.2mg−atomを加
え、液温20℃で2時間撹拌したところ、線状の金はすべ
て溶解した。
Example 29 To 10 g of water, 1 mmol of ammonium bromide and 0.5 mmol of bromine were added and dissolved, 0.2 mg-atom of 0.2 mmφ linear gold was further added, and the mixture was stirred at a liquid temperature of 20 ° C. for 2 hours. All the gold melted.

実施例30 メタノール10gに、メチルアミン塩酸塩1mmol及び塩素0.
5mmolを加えて溶解し、さらに0.2mmφの線状の金0.2mg
−atomを加え、液温20℃で3時間撹拌したところ、線状
の金はすべて溶解した。
Example 30 10 g of methanol, 1 mmol of methylamine hydrochloride and 0.
Add 5 mmol and dissolve, and 0.2 mg φ linear gold 0.2 mg
When -atom was added and the mixture was stirred at a liquid temperature of 20 ° C for 3 hours, all the linear gold was dissolved.

実施例31 メタノール10gに、ヨウ化テトラメチルアンモニウム1mm
ol及びヨウ素0.5mmolを加えて溶解し、さらに0.2mmφの
線状の金0.2mg−atomを加え、液温65℃で撹拌しながら
2時間還流加熱したところ、線状の金はすべて溶解し
た。
Example 31 Methanol 10 g, tetramethyl ammonium iodide 1 mm
ol and 0.5 mmol of iodine were added and dissolved, and 0.2 mg-atom of 0.2 mmφ linear gold was further added, and the mixture was heated under reflux for 2 hours with stirring at a liquid temperature of 65 ° C., and all the linear gold was dissolved.

実施例32 市販のヨードチンキ10ml(ヨウ素1.14mmol、ヨウ化カリ
ウム1.14mmol、メタノール変性エタノール7ml及び水2.5
2mlを含有)に、0.2mmφの線状の金0.2mg−atomを加
え、液温81℃で撹拌しながら1時間還流加熱したとこ
ろ、線状の金はすべて溶解した。
Example 32 Commercially available iodine tincture 10 ml (iodine 1.14 mmol, potassium iodide 1.14 mmol, methanol denatured ethanol 7 ml and water 2.5
0.2 mgφ linear gold 0.2 mg-atom was added to (containing 2 ml), and the mixture was heated under reflux for 1 hour with stirring at a liquid temperature of 81 ° C., and all the linear gold was dissolved.

〔発明の効果〕〔The invention's effect〕

本発明に係る金属の溶解方法は、実施例に示した通り、
操作が簡単であるうえ、数多くの金属に対して適用で
き、使用する可溶性ハロゲン化塩、ハロゲン単体及び極
性溶媒はいずれも安価なものである。従って、本方法に
よれば、経済的に金属の溶解ができる。
The method for melting a metal according to the present invention, as shown in Examples,
In addition to being easy to operate, it is applicable to many metals, and the soluble halide salt, simple substance of halogen, and polar solvent used are all inexpensive. Therefore, according to this method, the metal can be economically dissolved.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】金属を、(A)ハロゲン単体、(B)可溶
性ハロゲン化塩及び(C)水及び極性有機溶媒の少なく
とも一方から成る溶媒、に接触させることを特徴とする
金属の溶解方法。
1. A method for dissolving a metal, which comprises contacting the metal with (A) a halogen simple substance, (B) a soluble halogenated salt, and (C) a solvent comprising at least one of water and a polar organic solvent.
JP2124543A 1990-05-15 1990-05-15 Metal melting method Expired - Lifetime JPH0753892B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2124543A JPH0753892B2 (en) 1990-05-15 1990-05-15 Metal melting method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2124543A JPH0753892B2 (en) 1990-05-15 1990-05-15 Metal melting method

Publications (2)

Publication Number Publication Date
JPH0421726A JPH0421726A (en) 1992-01-24
JPH0753892B2 true JPH0753892B2 (en) 1995-06-07

Family

ID=14888083

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2124543A Expired - Lifetime JPH0753892B2 (en) 1990-05-15 1990-05-15 Metal melting method

Country Status (1)

Country Link
JP (1) JPH0753892B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994025633A1 (en) * 1993-04-27 1994-11-10 Japan As Represented By Director General Of Agency Of Industrial Science And Technology Method of dissolving and recovering metal
JP2666876B2 (en) * 1993-06-18 1997-10-22 工業技術院長 Gold refining method
JP3127240B2 (en) * 1995-10-25 2001-01-22 工業技術院長 Method for producing metal complex salt
JP7194975B2 (en) * 2018-09-21 2022-12-23 国立大学法人千葉大学 Method for recovering copper from chalcopyrite and solvent system used for the method
JP7705119B2 (en) * 2021-07-20 2025-07-09 国立大学法人千葉大学 Method for recovering nickel and/or cobalt

Also Published As

Publication number Publication date
JPH0421726A (en) 1992-01-24

Similar Documents

Publication Publication Date Title
US20250137090A1 (en) Compositions and processes for the extraction of metals using non-aqueous solvents
KR20160127088A (en) Wet based formulations for the selective removal of noble metals
US4107261A (en) Process for the separation of platinum group metals
JPH0753892B2 (en) Metal melting method
Rossi et al. Photostimulated reactions of potassium diphenylarsenide with haloarenes by the SRN1 mechanism
US4919716A (en) Method for dissolution of metal
US5264191A (en) Quaternary ammonium trihalide and method for dissolution of metal with liquid containing the compound
JP2666876B2 (en) Gold refining method
JP2535743B2 (en) Method for extracting gold and silver from ore
JPH0819492B2 (en) Metal melting method
JPS634028A (en) How to treat scrap containing rare earths and iron
JPH03158422A (en) Method for melting metal
JPH0747783B2 (en) Metal melting method
JPH0694577B2 (en) Metal melting method
JPH01190601A (en) Production of clathrate compound
JP3837879B2 (en) Method for reducing and precipitating metal ions
US3627651A (en) Synthesis of n:n{40 -disubstituted bipyridylium salts
JP3479677B2 (en) Method for selectively recovering copper ions from alkaline solution
Hirai et al. Extraction of vanadium (V) from hydrochloric acid by tri-n-octylmethylammonium chloride
JP4699622B2 (en) Method for separating boron-containing solution from R (rare earth) -Fe-B magnet alloy sludge
JPH1112664A (en) Noble metal separating and recovering agent
JP2629069B2 (en) Method for producing metal halide phthalocyanine
AU619680B2 (en) Compositions and method for recovery of gold and silver from sources thereof
US20160289170A1 (en) N-Substituted Glycinium (Fluorosulfonyl)(Trifluoromethylsulfonyl)imide Compound
JP2014118585A (en) Method for recovering ruthenium from a ruthenium-containing aqueous alkali solution

Legal Events

Date Code Title Description
EXPY Cancellation because of completion of term