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US2186293A - Decomposition of nickel-copper matte - Google Patents

Decomposition of nickel-copper matte Download PDF

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Publication number
US2186293A
US2186293A US246062A US24606238A US2186293A US 2186293 A US2186293 A US 2186293A US 246062 A US246062 A US 246062A US 24606238 A US24606238 A US 24606238A US 2186293 A US2186293 A US 2186293A
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United States
Prior art keywords
nickel
chloride
copper
solution
matte
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Expired - Lifetime
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US246062A
Inventor
Hamprecht Guenther
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IG Farbenindustrie AG
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IG Farbenindustrie AG
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Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B15/00Obtaining copper
    • C22B15/0063Hydrometallurgy
    • C22B15/0065Leaching or slurrying
    • C22B15/0067Leaching or slurrying with acids or salts thereof
    • C22B15/0069Leaching or slurrying with acids or salts thereof containing halogen
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B23/00Obtaining nickel or cobalt
    • C22B23/04Obtaining nickel or cobalt by wet processes
    • C22B23/0407Leaching processes
    • C22B23/0415Leaching processes with acids or salt solutions except ammonium salts solutions
    • C22B23/0423Halogenated acids or salts thereof
    • 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

Definitions

  • nickel-copper matte of any composition can be decomposed in a very short time with copper chloride solution nearly completely without any need for adding calcium chloride or sodium chloride by taking care that the solution contains such an amount of nickel chloride that the cuprous chloride formed remains dissolved.
  • the residue contains besides the sulphur content of the matte a little copper sulphide and a considerable amount of the precious metals originally contained in the matte.
  • the ratio between nickel and copper corresponds to the ratio between the two metals present in the matte.
  • care is preferably taken'that the ratio of nickel to. copper in the solution is greater than the ratio in the matte.
  • the new process has the great advantage that very pure solutions can be directly obtained which may be worked up for example electrolytically.
  • Example 1 cubic meters of a solution, warmed to 70 centigrade, of 440 grams of nickel chloride and 310 grams of copper chloride per liter are brought together with 2.67 metric tons of finely broken (or better, ground) nickel-copper matte containing 42 per cent of nickel, 47 per cent of copper and 10 per cent of sulphur into a slowly rotating inclined drum.
  • the solution becomes heated very rapidly to 100 centigrade and already after 10 minutes the resulting solution of nickel chloride and cuprous chloride may be filtered off from the residue,'consisting mainly ofsulphur, without the occurrence of difilculty by reason of the precipi-' tation of cuprous chloride.
  • the solution now contains about 540 grams of nickel chloride and 300 grams of cuprous chloride per liter. It may be worked up electrolytically to metallic nickel and copper in known manner.
  • the initial solution is recovered in the following manner: The chlorine set free during the electrolysis of the nickel chloride is led into the nickel chloride-cuprous chloride solution partially oxidized anodically coming from the copper electrolysis and the necessary amount of nickel chloride is added to the solution in the form of dilute electrolysis waste liquor.
  • Example 2 40 cubic meters of a solution, warmed to 95" centigrade, of 470 grams of. nickel chloride and 190 grams of copper chloride per liter is brought together with 2.47 metric tons of finely ground nickel-copper matte containing about 56 per cent of nickel, 24 per cent of copper and 20 per cent of sulphur into a slowly rotated inclined be worked up into nickel and copper in the manner described in Example 1.
  • Example 1 In order to recover the initial solution, the procedure described in Example 1 is followed but a special addition of nickel chloride is unnecessary in this case.
  • a process for the decomposition of nickelcopper matte which consists in using as the decomposing agent a copper chloride solution containing an amount of nickel chloride sufiicient to keep the cuprous chloride formed dissolved.
  • a process or the decomposition of nickel copper matte which consists in using as the decomposing agent a copper chloride solution containing adequate nickel chloride to keep the cuprous chloride formed dissolved and making the ratiohetween nickel and copper in the decomposing solution equal to the ratio between the two metals present in the matte.

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electrolytic Production Of Metals (AREA)

Description

Patented Jan. 9, 1940 UNITED STATES PATENT OFFICE nnoom-osrnon 0F NICKEL-COPPER mm Guenther Hamprechh. Ludwigshaien-on-the- Rhine, Germany, assignor to I. G. Farbenin- Y dustrie Aktiengesellschaft;\FranHoi-t-on-the- Main, Germany No Drawing. Application December 1t, 1938, Serial No. 246,062. In Germany December 20,
2 Claims.
iron and the gangue, a matte for the working up of which various proposals have been made. For example it has been proposed to treat the matte with chlorine and copper chloride solution containing such an amount of calcium chloride or sodium chloride that the cuprous chloride formed is not precipitated. The resulting solution is then worked up electrolytically to metallic copper and nickel, the initial solution thus being recovered in addition to chlorine. This processhas not been introduced in practice because the decomposition of the matte offers difficulty.
I have now found that nickel-copper matte of any composition can be decomposed in a very short time with copper chloride solution nearly completely without any need for adding calcium chloride or sodium chloride by taking care that the solution contains such an amount of nickel chloride that the cuprous chloride formed remains dissolved. The residue contains besides the sulphur content of the matte a little copper sulphide and a considerable amount of the precious metals originally contained in the matte.
The following table gives the approximate minimum amounts of nickel chloride which the solution must contain at centigrade in order that the given amounts of cuprous chloride should remain dissolved at the said temperature:
Grams of NiClz Grams oi. CuCl per liter per liter 220 80 330 170 440 225 At higher temperatures, correspondingly less amounts of nickel chloride are necessary for this Purpose.
In the working up of mattes rich in nickel, as for example those containing more than about 45 per cent of nickel, it is preferable so to select the composition of the nickel chloride-copper chloride solution acting on the matte that the ratio between nickel and copper corresponds to the ratio between the two metals present in the matte. In the case of mattes poor in nickel, care is preferably taken'that the ratio of nickel to. copper in the solution is greater than the ratio in the matte.
The new process has the great advantage that very pure solutions can be directly obtained which may be worked up for example electrolytically.
The following examples will further illustrate the nature of this invention but the invention is not restricted to these examples.
Example 1 cubic meters of a solution, warmed to 70 centigrade, of 440 grams of nickel chloride and 310 grams of copper chloride per liter are brought together with 2.67 metric tons of finely broken (or better, ground) nickel-copper matte containing 42 per cent of nickel, 47 per cent of copper and 10 per cent of sulphur into a slowly rotating inclined drum. The solution becomes heated very rapidly to 100 centigrade and already after 10 minutes the resulting solution of nickel chloride and cuprous chloride may be filtered off from the residue,'consisting mainly ofsulphur, without the occurrence of difilculty by reason of the precipi-' tation of cuprous chloride.
The solution now contains about 540 grams of nickel chloride and 300 grams of cuprous chloride per liter. It may be worked up electrolytically to metallic nickel and copper in known manner.
The initial solution is recovered in the following manner: The chlorine set free during the electrolysis of the nickel chloride is led into the nickel chloride-cuprous chloride solution partially oxidized anodically coming from the copper electrolysis and the necessary amount of nickel chloride is added to the solution in the form of dilute electrolysis waste liquor.
Example 2 40 cubic meters of a solution, warmed to 95" centigrade, of 470 grams of. nickel chloride and 190 grams of copper chloride per liter is brought together with 2.47 metric tons of finely ground nickel-copper matte containing about 56 per cent of nickel, 24 per cent of copper and 20 per cent of sulphur into a slowly rotated inclined be worked up into nickel and copper in the manner described in Example 1.
In order to recover the initial solution, the procedure described in Example 1 is followed but a special addition of nickel chloride is unnecessary in this case.
What I claim is;
1. A process for the decomposition of nickelcopper matte, which consists in using as the decomposing agent a copper chloride solution containing an amount of nickel chloride sufiicient to keep the cuprous chloride formed dissolved.
2. A process or the decomposition of nickel copper matte, which consists in using as the decomposing agent a copper chloride solution containing suficient nickel chloride to keep the cuprous chloride formed dissolved and making the ratiohetween nickel and copper in the decomposing solution equal to the ratio between the two metals present in the matte.
GUENTHER HANEPRECI-I'I.
US246062A 1937-12-20 1938-12-16 Decomposition of nickel-copper matte Expired - Lifetime US2186293A (en)

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Application Number Priority Date Filing Date Title
DE2186293X 1937-12-20

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0043646A1 (en) * 1980-06-03 1982-01-13 The International Metals Reclamation Company Inc. Separation of chromium from scrap
CN115341097A (en) * 2022-01-30 2022-11-15 昆明理工大学 Method for treating high-arsenic low-mercury selenic acid sludge through hydrometallurgy

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0043646A1 (en) * 1980-06-03 1982-01-13 The International Metals Reclamation Company Inc. Separation of chromium from scrap
CN115341097A (en) * 2022-01-30 2022-11-15 昆明理工大学 Method for treating high-arsenic low-mercury selenic acid sludge through hydrometallurgy
CN115341097B (en) * 2022-01-30 2024-03-26 昆明理工大学 A method for hydrometallurgical treatment of high arsenic and low mercury selenate mud

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