JPH0753892B2 - Metal melting method - Google Patents
Metal melting methodInfo
- 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
Links
- 229910052751 metal Inorganic materials 0.000 title claims description 39
- 239000002184 metal Substances 0.000 title claims description 39
- 238000000034 method Methods 0.000 title claims description 15
- 238000002844 melting Methods 0.000 title description 4
- 230000008018 melting Effects 0.000 title description 4
- 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 7
- 150000003839 salts Chemical class 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 239000003495 polar organic solvent Substances 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 13
- 229910052737 gold Inorganic materials 0.000 description 13
- 239000010931 gold Substances 0.000 description 13
- 239000007788 liquid Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- 239000002798 polar solvent Substances 0.000 description 9
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 9
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- -1 halide salt Chemical class 0.000 description 6
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- 229910052740 iodine Inorganic materials 0.000 description 5
- 239000011630 iodine Substances 0.000 description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
- 229910052794 bromium Inorganic materials 0.000 description 4
- 150000008282 halocarbons Chemical class 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 3
- 150000007522 mineralic acids Chemical class 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 235000009518 sodium iodide Nutrition 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-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
- 230000002378 acidificating effect Effects 0.000 description 2
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229910001622 calcium bromide Inorganic materials 0.000 description 2
- WGEFECGEFUFIQW-UHFFFAOYSA-L calcium dibromide Chemical compound [Ca+2].[Br-].[Br-] WGEFECGEFUFIQW-UHFFFAOYSA-L 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 238000011978 dissolution method Methods 0.000 description 2
- NQMRYBIKMRVZLB-UHFFFAOYSA-N methylamine hydrochloride Chemical compound [Cl-].[NH3+]C NQMRYBIKMRVZLB-UHFFFAOYSA-N 0.000 description 2
- RXMRGBVLCSYIBO-UHFFFAOYSA-M tetramethylazanium;iodide Chemical compound [I-].C[N+](C)(C)C RXMRGBVLCSYIBO-UHFFFAOYSA-M 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 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
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 229910001420 alkaline earth metal ion Inorganic materials 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
- 125000004429 atom Chemical group 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
- 229940006460 bromide ion Drugs 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 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
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 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
- 229940075894 denatured ethanol Drugs 0.000 description 1
- 230000000694 effects Effects 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
- 125000005843 halogen group Chemical group 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 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
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
- 229940006461 iodide ion Drugs 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 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
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 239000010955 niobium Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 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
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 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
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 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
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 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
【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.
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).
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.
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.
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.
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)
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.
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)
| 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 |
-
1990
- 1990-05-15 JP JP2124543A patent/JPH0753892B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0421726A (en) | 1992-01-24 |
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