JPH0747783B2 - Metal melting method - Google Patents
Metal melting methodInfo
- Publication number
- JPH0747783B2 JPH0747783B2 JP3027656A JP2765691A JPH0747783B2 JP H0747783 B2 JPH0747783 B2 JP H0747783B2 JP 3027656 A JP3027656 A JP 3027656A JP 2765691 A JP2765691 A JP 2765691A JP H0747783 B2 JPH0747783 B2 JP H0747783B2
- Authority
- JP
- Japan
- Prior art keywords
- metal
- organic solvent
- added
- halogen
- polar organic
- 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
Links
- 229910052751 metal Inorganic materials 0.000 title claims description 37
- 239000002184 metal Substances 0.000 title claims description 37
- 238000000034 method Methods 0.000 title claims description 14
- 238000002844 melting Methods 0.000 title description 2
- 230000008018 melting Effects 0.000 title description 2
- 239000003495 polar organic solvent Substances 0.000 claims description 11
- 229910052736 halogen Inorganic materials 0.000 claims description 10
- 150000002367 halogens Chemical class 0.000 claims description 10
- 239000000126 substance Substances 0.000 claims description 8
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 238000004090 dissolution Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 150000008282 halocarbons Chemical class 0.000 description 4
- 229910052740 iodine Inorganic materials 0.000 description 4
- 239000011630 iodine Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 239000003093 cationic surfactant Substances 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 150000007522 mineralic acids Chemical class 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910001507 metal halide Inorganic materials 0.000 description 2
- 150000005309 metal halides Chemical class 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- -1 acetone Chemical compound 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000011978 dissolution method Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
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)
Description
【0001】[0001]
【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、ハロゲン単体の極性有機溶媒
溶液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。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for dissolving a metal, and more particularly to a method for dissolving a metal which is characterized by bringing the halogen into contact with a polar organic solvent solution.
【0002】[0002]
【従来の技術】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。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)。2. Description of the Related Art Dissolving a metal in a liquid is an essential step for extracting and recovering the metal from a mixture containing the metal and is extremely important industrially. 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. Further, 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).
【0003】[0003]
【発明が解決しようとする課題】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、使用
する陽イオン性界面活性剤が比較的高価であり、また、
溶媒が臭気と毒性の強いハロゲン化炭化水素であるた
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 waste water is generated, and a large amount of cost is required for the treatment of this waste water. Takes. Further, in the method of contacting with a halogenated hydrocarbon in the presence of a cationic surfactant, the cationic surfactant used is relatively expensive, and
Since the solvent is a halogenated hydrocarbon having a strong odor and toxicity, there are problems such as difficulty in working.
【課題を解決するための手段】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用いる金属の溶解方法
を求めて種々検討した結果、多くの金属が、ハロゲン単
体の極性有機溶媒溶液に接触させることにより溶解する
現象を見いだし、本発明に到達した。すなわち、本発明
は、ハロゲン単体の極性有機溶媒溶液に接触させること
を特徴とする金属の溶解方法を提供するものである。本
発明方法では、ハロゲン単体として、塩素、臭素または
ヨウ素の単体が用いられる。また、溶媒として極性有機
溶媒が用いられる。極性有機溶媒としては、たとえば、
アセトニトリルなどのニトリル類、メタノールなどのア
ルコール類、アセトンなどのケトン類、酢酸エチルなど
のエステル類をあげることができる。このような極性有
機溶媒は、ハロゲンをよく溶解し、同時に金属ハロゲン
化物もよく溶解するので、金属の溶解の溶媒として適し
ている。本発明方法においては、極性有機溶媒溶液中に
おいてハロゲン単体に金属を接触させることにより金属
をハロゲン化物に変換する。すなわち、目的の金属に対
し、ハロゲン単体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、これが極性有機溶媒
に溶解するわけである。金属の溶解に要する時間は、目
的とする金属、用いるハロゲンの種類及び濃度などによ
り異る。また、処理温度は極性有機溶媒の沸点以下の範
囲で選ばれるが、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
なることで確認できる。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、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、パラジウム、インジウム、錫、アン
チモン、テルル、ハフニウム、金、水銀、ビスマスなど
である。[Means for Solving the Problems] In order to solve the problems of the conventional methods, the present inventors have made various investigations for a method of dissolving a metal using an organic solvent other than a halogenated hydrocarbon without using an inorganic acid. As a result, they found that many metals dissolve when they are brought into contact with a polar organic solvent solution of a simple substance of halogen, and the present invention has been accomplished. That is, the present invention provides a method for dissolving a metal, which comprises contacting with a polar organic solvent solution of a simple substance of halogen. In the method of the present invention, a simple substance of chlorine, bromine or iodine is used as a simple substance of halogen. A polar organic solvent is used as the solvent. As the polar organic solvent, for example,
Examples thereof include nitriles such as acetonitrile, alcohols such as methanol, ketones such as acetone, and esters such as ethyl acetate. Such a polar organic solvent dissolves halogen well, and at the same time dissolves metal halide well, and is therefore suitable as a solvent for dissolving metal. In the method of the present invention, a metal is converted to a halide by bringing the metal into contact with a simple substance of halogen in a polar organic solvent solution. That is, when a halogen atom is given to a target metal from a simple substance of halogen, a metal halide is generated, and this is dissolved in a polar organic solvent. The time required to dissolve the metal depends on the target metal, the type and concentration of the halogen used, and the like. Further, the treatment temperature is selected within a range not higher than the boiling point of the polar organic solvent, and the higher the treatment temperature is, the more the dissolution of the metal is promoted. The end point of melting of the metal can be confirmed by disappearing the charged metal. The metals dissolved by the process of the present invention include both typical metals and transition metals, such as beryllium, magnesium, aluminum, vanadium, chromium, manganese, iron, cobalt, nickel,
Examples include copper, zinc, selenium, palladium, indium, tin, antimony, tellurium, hafnium, gold, mercury and bismuth.
【0004】[0004]
【実施例】次に、実施例により本発明をさらに詳しく説
明する。EXAMPLES Next, the present invention will be described in more detail by way of examples.
【実施例1〜15】アセトニトリル10g に臭素0.5m
molを加えて溶解し、さらに表1に示す金属の粉末0.2
mg-atom を加えてかくはんしながら、液温80℃で還流
加熱した。ここで、金属の粉末が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、この
残査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 15 0.5 g of bromine in 10 g of acetonitrile
0.2 mol of metal powder shown in Table 1 was added and dissolved.
While stirring by adding mg-atom, the mixture was heated under reflux at a liquid temperature of 80 ° C. Here, when the metal powder does not remain, the dissolution rate is set to 100%, and when there is a metal residue, this residue is separated from the solution by decanting, washed with methanol, dried, and then weighed. . 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16〜21】アセトニトリル10g に塩素
0.5mmolを加えて溶解し、さらに表2に示す0.2mmφの
線状の金属0.2mg-atom を加えて30℃でかくはんし
たところ、溶解率は次の通りであった。 Examples 16 to 21 0.5 mmol of chlorine was added to and dissolved in 10 g of acetonitrile, 0.2 mg-atom of 0.2 mmφ linear metal shown in Table 2 was added, and the mixture was stirred at 30 ° C. It was as follows.
【実施例22〜25】メタノール10g に臭素0.5mmo
lを加えて溶解し、さらに表3に示す 0.2mmφの線状の
金属0.2mg-atom を加えて30℃でかくはんしたとこ
ろ、溶解率は次の通りであった。 Examples 22 to 25 Bromine 0.5 mmo in 10 g of methanol
l was added and dissolved, and 0.2 mgφ linear metal 0.2 mg-atom shown in Table 3 was further added and stirred at 30 ° C. The dissolution rate was as follows.
【実施例26〜27】アセトン10g にヨウ素0.5mmo
lを加えて溶解し、さらに表4に示す 0.2mmφの線状の
金属0.2mg-atomを加えて、かくはんしながら液温56
℃で還流加熱したところ、溶解率は次の通りであった。 Examples 26 to 27 Iodine 0.5 mmo in 10 g of acetone
l was added and dissolved, and 0.2 mg-linear metal 0.2 mg-atom shown in Table 4 was further added, and the liquid temperature 56 while stirring.
Upon heating under reflux at ℃, the dissolution rate was as follows.
【実施例28】アセトニトリル10g にヨウ素0.5mmo
lを加えて溶解し、さらに水銀 0.2mg-atom を加えて
かくはんしながら、液温80℃で1時間還流加熱したと
ころ水銀はすべて溶解した。Example 28 Iodine 0.5 mmo in 10 g of acetonitrile
When 1 ml was added and dissolved, and then 0.2 mg-atom of mercury was added and the mixture was stirred and refluxed at a liquid temperature of 80 ° C. for 1 hour, all the mercury was dissolved.
【実施例29】酢酸エチル10g にヨウ素0.5mmolを
加えて溶解し、さらに0.2mmφの線状の鉄0.2mg-atom
を加えてかくはんしながら液温77℃で0.5時間還流
加熱したところ鉄はすべて溶解した。Example 29 0.5 mmol of iodine was added to and dissolved in 10 g of ethyl acetate, and 0.2 mg-atom of 0.2 mmφ linear iron was added.
Was added and stirred under reflux at a liquid temperature of 77 ° C. for 0.5 hour to dissolve all iron.
【0005】[0005]
【発明の効果】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、使用するハロゲン単体及び極性有機溶
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。As described in the examples, the method for dissolving a metal according to the present invention is simple in operation and can be applied to many metals. Both halogen simple substance and polar organic solvent used are inexpensive. It is something. Therefore, according to this method, the metal can be economically dissolved.
Claims (1)
液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 bringing the metal into contact with a polar organic solvent solution of a simple substance of halogen.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3027656A JPH0747783B2 (en) | 1991-01-30 | 1991-01-30 | Metal melting method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3027656A JPH0747783B2 (en) | 1991-01-30 | 1991-01-30 | Metal melting method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH04246135A JPH04246135A (en) | 1992-09-02 |
| JPH0747783B2 true JPH0747783B2 (en) | 1995-05-24 |
Family
ID=12226975
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3027656A Expired - Lifetime JPH0747783B2 (en) | 1991-01-30 | 1991-01-30 | Metal melting method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0747783B2 (en) |
-
1991
- 1991-01-30 JP JP3027656A patent/JPH0747783B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH04246135A (en) | 1992-09-02 |
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