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WO2006029246A1 - Installation for continuous fire refining of copper - Google Patents

Installation for continuous fire refining of copper Download PDF

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Publication number
WO2006029246A1
WO2006029246A1 PCT/US2005/031945 US2005031945W WO2006029246A1 WO 2006029246 A1 WO2006029246 A1 WO 2006029246A1 US 2005031945 W US2005031945 W US 2005031945W WO 2006029246 A1 WO2006029246 A1 WO 2006029246A1
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WO
WIPO (PCT)
Prior art keywords
copper
furnace
reduction
continuous
launder
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.)
Ceased
Application number
PCT/US2005/031945
Other languages
French (fr)
Inventor
Gabriel Riveros
Andrzej Warczok
Tanai Marin
Hermann Schwarze
Jose Sanhueza
Daniel Smith
Ariel Balocci
Luis Gonzalez
Stephan Wallner
Andreas Fiellzwieser
Patricio Grau
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.)
RHI NON FERROUS METALS ENGINEERING GmbH
EMPRESA NACIONAL DE MINERIA ENAMI
Universidad de Chile
WEISZ TIBERIU
Original Assignee
RHI NON FERROUS METALS ENGINEERING GmbH
EMPRESA NACIONAL DE MINERIA ENAMI
Universidad de Chile
WEISZ TIBERIU
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 RHI NON FERROUS METALS ENGINEERING GmbH, EMPRESA NACIONAL DE MINERIA ENAMI, Universidad de Chile, WEISZ TIBERIU filed Critical RHI NON FERROUS METALS ENGINEERING GmbH
Priority to MX2007002782A priority Critical patent/MX2007002782A/en
Priority to EP05794326A priority patent/EP2111471A4/en
Priority to CA2579586A priority patent/CA2579586C/en
Priority to AU2005282368A priority patent/AU2005282368B2/en
Publication of WO2006029246A1 publication Critical patent/WO2006029246A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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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
    • C22B15/0026Pyrometallurgy
    • C22B15/006Pyrometallurgy working up of molten copper, e.g. refining
    • 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
    • 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
    • C22B15/0026Pyrometallurgy
    • C22B15/0028Smelting or converting
    • C22B15/005Smelting or converting in a succession of furnaces
    • 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
    • C22B15/0026Pyrometallurgy
    • C22B15/0028Smelting or converting
    • C22B15/0052Reduction smelting or converting
    • 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

  • This invention relates to an apparatus for continuous fire refining of blister copper or secondary copper.
  • Fire refining of blister copper is carried out in stationary reverberatory or vascular furnaces, called anode furnaces due to the most common casting of refined copper in the form of anodes, which are transferred to electrolytical refining.
  • Fire refining process is a classical batch process consisting of four stages: charging, oxidation and impurities slagging, reduction and anode casting. Time of refining cycle without the stage of melting varies from 6 to 14 hours.
  • Oxidized copper after oxidation stage contains from 5000 to 10000 ppm of oxygen.
  • the copper is reduced by carboneous or amonia reductant.
  • the most common reductant in use are the oil or natural gas.
  • the oil or natural gas are injected with air into the bath of molten copper through a tuyere or tuyeres.
  • Copper reduction faces significant limitations in the process rate and efficiency of reductant utilisation.
  • Reduction stage of the liquid copper charge which fluctuates from 150 to 400 t, varies in the range from 1.2 to 2.0 hours.
  • Reported reductant efficiency is below 50%.
  • Injection of liquid or gaseous reductant into the copper produces black fumes in off-gas due to thermal decomposition of hydrocarbons. Partial carbon utilisation in oxygen reduction from copper causes the presence of carbon particles in the reduction gases, which are partly combusted if the burner flame is oxidising.
  • Patent N 0 2.989.397 June 1961.
  • the study showed that the injection of natural gas with air states a better solution than the injection of only natural gas into a liquid copper.
  • Method of deoxidization of copper with reformed natural gas and related apparatus have been patented by Phelps Dodge Corporation in USA and Canada.
  • C.Kuzell, M. Fowler, S. Davis y L. Klein "Apparatus for reforming gases" U.S. Patent N 0 3.071.454, January 1963; "Gaseous reduction of oxygen containing copper", Canadian Patent N° 668.598, August 1963)
  • R. Nenych, F. Kadler and V. Sedlacek replaced the conventional reduction with wood by ammonia, what allowed for production of high quality copper.
  • Ammonia consumption is about 1 kg/t of copper , when oxygen is reduced from 4000 a 1000 ppm.
  • N. Themelis and P.Schmidt have patented the deoxidisation of a liquid copper by injection of various reformed hydrocarbons (methane, ethane, butane) with steam, leading to the formation of the gas containing carbon monoxide and hydrogen. Patented installation was based on vascular furnace. ( "Apparatus and process for the gaseous deoxidisation of molten metal, Canadian Patent N 0 827.066, November 1969).
  • Figure 1 is a sketch illustrating schematically the principle of intensive, continuous fire refining of blister copper supplied from continuous Mitsubishi copper matte converting furnace.
  • This invention refers to a pirometallurgical method of oxygen removal from a liquid copper by the use of solid carboneous reductant, charged on the surface of copper in addition to the injection of reductant through tuyeres or lances and simultaneous agitation of copper bath with inert gas introduced via porous plugs.
  • the method in which carboneous reductant and hydrocarbons of oil or natural gas mixed with air or steam react with oxygen dissolved in copper results in high rate of reduction, shorten the time and increase of reductant efficiency.
  • the invention leading to a method of oxygen extraction from a liquid copper consists of following stages:
  • copper reduction (4) after oxidation and slagging of impurities, is carried out by injection of a liquid or gaseous reductant (oil, natutral gas) (3) with simultaneous addition of solid reductant (5) onto copper bath surface(4) and bath agitation with inert gas (1) through porous plugs (2)
  • a liquid or gaseous reductant oil, natutral gas
  • inert gas (1) Injection of inert gas (1) through the porous plug (2) prevents the formation of the gradient of oxygen content in the copper slowing down the rate of reaction. Continuous stirring of the copper bath in whole volume by inert gas (1) ensures the mass transfer onto the reaction surface (copper/charcoal).
  • Floating charcoal or coke bed (5) on the copper (4) surface allows for higher flexibility of burner operation. Even in the case of oxidising flame the charcoal (5) is protecting copper against the oxidation, permitting for more efficient use of fuel and better control of copper temperature. Moreover, the excess oxygen in the burner allows for post-combustion of reduction gases (7) leaving the bath producing clean gases.
  • This invention has following advantages compared with traditional methods of copper reduction: a) Application of solid carbon addition combined with bath stirring by nitrogen introduced by porous plugs during injection of liquid or gaseous reductant significantly shorten reduction time from 40 to 60% in comparison to common reduction practice. b) Efficiency of reductant (carbon and hydrocarbons) increases from 30 to 50% of the average values of traditional operation. c) Emission of gases with black fumes (carbon black) is drastically decreased reducing negative process impact on the environment. d) Higher reductant efficiency and shorter reduction time results in the decrease of unitary reductant and fuel consumption as well as in the increase of furnace productivity, e) Cost of method application is low. Necessary modifications of refining furnace are minor. f) EXAMPLE 1
  • Copper refining is carried out in vascular anode furnace capacity of 150 t of copper as it is schematically illustrated in Figure 1.
  • Four porous plugs (2) are mounted in the bottom part of the furnace.
  • nitrogen (1) is injected into the molten copper (4).
  • Nitrogen flowrate varies from 40 to 120 NmVh.
  • Oxidation period is ended by skimming out of the slag.
  • Oxygen content in the copper is in the level of 8000 ppm.
  • 1.5 to 4 kg of charcoal (5) per tonne of copper is charged through the mouth onto copper surface.
  • Copper refining is carried out in stationary anode furnace of capacity 300 t of copper.
  • porous plugs are installed in the bottom part of side wall against the wall with charging window. Nitrogen flowrate through porous plug is 0.3 - 1.0 NmVh per tonne of copper. After finishing oxidation period and skimming out of refining slag the portion of 1.3 - 4.0 kg of charcoal per tonne of copper is charged through a window onto the copper surface.
  • the oil flow is put on through a lance (2 - 5 kg/h per tonne of copper) together with air (2 - 5 Nm 3 /h tonne of copper). Lance is immersed into the copper and reduction. Burner is supplied by natural gas.
  • Burner parameters are set: 1 - 3 Nm 3 /h of natural gas and 7 - 20 NmVh of air per tonne of copper. It ensures effective post-combustion of reduction gases and emission of clean off-gas to the atmosphere. After 100 min the lance is removed and the oil and air flows shut down. Oxygen content has been decreased from 6000 - 8000 ppm to about 400 - 800 ppm. Next, anode casting is proceeded.

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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)
  • Manufacture And Refinement Of Metals (AREA)

Abstract

An installation for continuous copper fire refining, said system comprising the components: launder (4) transferring liquid blister copper from continuous converting furnace or from retention furnace into a first oxidation reactor; copper oxidation reactor (7); optionally settler separating oxidized copper and slag; launder (8) transferring oxidized copper from oxidation reactor into reduction reactor; copper reduction reactor (12); and launder (14) transferring reduced copper from reduction reactor to casting will or to retention-casting furnace.

Description

INSTALLATION FOR CONTINUOUS FIRE REFINING OF COPPER
BACKGROUND OF INVENTION
1. Field of Invention:
This invention relates to an apparatus for continuous fire refining of blister copper or secondary copper.
2. Description of the Prior Art:
Smelting of copper concentrates produces matte and slag. Copper matte is converted into blister copper in Peirce-Smith, Hoboken converters or continuous converting processes such as Kennecott-Outokumpu or Mitsubishi. Blister copper is directed to fire refining process prior electrorefining.
Fire refining of blister copper is carried out in stationary reverberatory or vascular furnaces, called anode furnaces due to the most common casting of refined copper in the form of anodes, which are transferred to electrolytical refining. Fire refining process is a classical batch process consisting of four stages: charging, oxidation and impurities slagging, reduction and anode casting. Time of refining cycle without the stage of melting varies from 6 to 14 hours.
Oxidized copper after oxidation stage contains from 5000 to 10000 ppm of oxygen. The copper is reduced by carboneous or amonia reductant. The most common reductant in use are the oil or natural gas. The oil or natural gas are injected with air into the bath of molten copper through a tuyere or tuyeres. Copper reduction faces significant limitations in the process rate and efficiency of reductant utilisation. Reduction stage of the liquid copper charge, which fluctuates from 150 to 400 t, varies in the range from 1.2 to 2.0 hours. Reported reductant efficiency is below 50%. Injection of liquid or gaseous reductant into the copper produces black fumes in off-gas due to thermal decomposition of hydrocarbons. Partial carbon utilisation in oxygen reduction from copper causes the presence of carbon particles in the reduction gases, which are partly combusted if the burner flame is oxidising.
- l -
SUBSTITUTE SHET (RULE 26) Carbon particles are transferred to the furnace off-gas, creating black fumes emitted through a chimney to the atmosphere.
Reduction of a liquid oxidised copper is practised for centuries and it was first described by Georgious Agricola (G:Agricola: "De Re Metallica", translated from latin, la edition 1556 por Hebert C. Hoover y Lou H. Hoover, Dover Publications, 1950, 535-536). After copper oxidition with air in open hearth furnace and removal of impurities, the copper was reduced with a wood.. Copper reduction with wood (poling) is still practised in some smelters. L.Klein presented a new idea of the use of gas reductant as a substitute of a wood. ( "Gaseous reduction of oxygen-containing copper", J. of Metals, VoI 13, N°8, August 1961, 545-547 ; U.S. Patent N0 2.989.397, June 1961). The study showed that the injection of natural gas with air states a better solution than the injection of only natural gas into a liquid copper. Method of deoxidization of copper with reformed natural gas and related apparatus have been patented by Phelps Dodge Corporation in USA and Canada. (C.Kuzell, M. Fowler, S. Davis y L. Klein: "Apparatus for reforming gases" U.S. Patent N0 3.071.454, January 1963; "Gaseous reduction of oxygen containing copper", Canadian Patent N° 668.598, August 1963)
R. Nenych, F. Kadler and V. Sedlacek replaced the conventional reduction with wood by ammonia, what allowed for production of high quality copper. Ammonia consumption is about 1 kg/t of copper , when oxygen is reduced from 4000 a 1000 ppm. (R. Henych et al., "Copper refining by gaseous ammonia", J. of Metals, VoI 17, N°4, April 1955). N. Themelis and P.Schmidt have patented the deoxidisation of a liquid copper by injection of various reformed hydrocarbons (methane, ethane, butane) with steam, leading to the formation of the gas containing carbon monoxide and hydrogen. Patented installation was based on vascular furnace. ( "Apparatus and process for the gaseous deoxidisation of molten metal, Canadian Patent N0 827.066, November 1969).
R.Beck, C.Andersen and M. Messner have patented the process of copper deoxidisation with the mix of natural gas/air. ("Process for deoxidising copper with natural gas-air mixture, U.S. Patent N° 3.619.177, November 1971). Anaconda Company patented a process of copper deoxidisation in vascular furnace by injection through lances of the mix of natural gas or Diesel oil and water vapour (W. Foard and R. Lear: "Refining copper" U.S.Patent N°3,529.956, September, 1970). J. Henderson and W. Johnson have patented for ASARCO the method of copper reduction in a vascular furnace by natural gas injection through tuyeres ("Gas poling of copper", U.S.Patent N0 3.623.863, November 1971).
G. Mckerrow and D. Panell reviewed in a paper "Gaseous deoxidization of anode copper at the Noranda smelter" Canadian Metallurgical Quarterly, VoI 11, N°4, 1972, 629-633, the evolution of methods of copper deoxidization in Noranda smelter using natural gas injected through tuyeres in a vascular furnace. J. Oudiz made a general review of copper reduction processes ("Poling processes for copper refining", J. of Metals, VoI 25, December 1973, 35-38). Based on industrial data the consumption of reductant, benefits and problems related with the use of various reductants, reforming reactions and reductant efficiency have been analyzed. L.Lavrov ("Deoxidization of anode copper by natural gas and steam mixture", The Soviet
Journal of Non-Ferrous Metals, VoI N019, N°5, English translation, May 1978, 25-26) veryfied the use of a mix od natural gas and steam injected through a lance.
C. Toro and V. Paredes ("Sustituciόn parcial del petrόleo diesel por Enap-6 como agente reductor en Ie proceso de obtenciόn de cobre anόdico en Ia fundiciόn Potrerillos", 34 a Convenciόn Anual IIMCh, Noviembre 1983, Rancagua) developed in industrial scale and demonstrated the possibilities of the use of heavy oil (ENAP-6), with higher sulphur content and lower price, in copper reduction.
J. Minoura ("Bunker fuel oil poling in anode furnace at Kosaka smelter", 114th AIME Annual Meeting, 1985, NY, USA) describes the copper reduction with heavy oil (Bunker C), showing the advantages and lower costs with comparison of copper reduction with ammonia practiced since 1967.
Referencies related to the use of porous plugs in copper fire refining are fragmentary since
1980 decade (P. Goyal, N. Themelis and W. Zanchuk, "Gaseous refining of anode copper", J. of Metals, VoI 34, December 1982, 22-28; P. Goyal, S. Joshi and J. Wang "Porous plug injection in anode refining furnace", J. of Metals, VoI 35, December 1983, 52-58). The porous plugs use was transferred from iron metallurgy and developed next in the area of metal casting. Industrial applications in copper refining were oriented first to copper desulphurisation by nitrogen stirring. The idea of copper reduction with hydrogen introduced via porous plugs was investigated only in laboratory scale. Description of industrial operation of porous plugs is presented in a paper of A, Rigby y M. Lanyi: "Porous plug in molten copper production and refining", CIM' 96, August 1996, 393-403.
Operational practice and proposed methods of injection, bath agitation and type of reductant, point out the existing problems in oxygen removal from a liquid copper, such as long reduction time, low reductant efficiency and emission of the gases with non- combusted particles.
SUMMARY OF INVENTION
It is an object of invention to provide a new method of continuous copper fire refining. This method is attained by a method, which uses solid additional reductant floating on the copper surface with simultaneous bath stirring by the inert gas supplied by porous plugs.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is a sketch illustrating schematically the principle of intensive, continuous fire refining of blister copper supplied from continuous Mitsubishi copper matte converting furnace.
DETAILED DESCRIPTION OF INVENTION
This invention refers to a pirometallurgical method of oxygen removal from a liquid copper by the use of solid carboneous reductant, charged on the surface of copper in addition to the injection of reductant through tuyeres or lances and simultaneous agitation of copper bath with inert gas introduced via porous plugs. The method in which carboneous reductant and hydrocarbons of oil or natural gas mixed with air or steam react with oxygen dissolved in copper results in high rate of reduction, shorten the time and increase of reductant efficiency.
Thus, the invention leading to a method of oxygen extraction from a liquid copper consists of following stages:
a) Oxidation of copper bath to the level necessary for impurities removal; b) Addition of carboneous reductant onto copper surface, injection of the mix fuel reductat through tuyere(s) and agitacion of bath by nitrogen via porous plugs; c) Continuation of oxygen extraction from a copper up to the desire oxygen content.
According to this invention, copper reduction (4), after oxidation and slagging of impurities, is carried out by injection of a liquid or gaseous reductant (oil, natutral gas) (3) with simultaneous addition of solid reductant (5) onto copper bath surface(4) and bath agitation with inert gas (1) through porous plugs (2)
Injection of a liquid or gaseous reductant with deficient amount of air (3) into the liquid copper (4) produces chemical reactions in the gaseous jet from tuyere and generated gas bubbles (9) rising up: • Decomposition of hydrocarbons CnHn, => n C + m H2
• Partial combustion with air 2 C + O2 => 2 CO
2 H2 + O2 => H2O
• Reduction of copper (O)COpPer + C => CO
(O) copper + CO => CO2 (O) copper + H2 => H2O
Addition of charcoal or another solid carboneous reductant on the surface of copper bath initiates the reactions at the copper/carbon interface:
(O copper + C => CO
(O) copper + CO => CO2 CO2 + C => 2 CO
Injection of inert gas (1) through the porous plug (2) prevents the formation of the gradient of oxygen content in the copper slowing down the rate of reaction. Continuous stirring of the copper bath in whole volume by inert gas (1) ensures the mass transfer onto the reaction surface (copper/charcoal).
Simultaneous copper (4) reduction by injected reductant (oil, natural gas) and floating bed of charcoal or coke increases significantly the total process rate, decreasing the time of reduction and increasing furnace productivity.
Floating charcoal or coke bed (5) on the copper (4) surface allows for higher flexibility of burner operation. Even in the case of oxidising flame the charcoal (5) is protecting copper against the oxidation, permitting for more efficient use of fuel and better control of copper temperature. Moreover, the excess oxygen in the burner allows for post-combustion of reduction gases (7) leaving the bath producing clean gases.
The major problem of copper (4) reduction by injection of oil or natural gas (3) is the formation and emission of black fumes. Thermal decomposition of hydrocarbons produces hydrogen and elemental carbon (9). Carbon particles are partly reacting with oxygen from copper, but partly are rising up inside the bubbles being released from the melt. This part of carbon can be partly combusted over the melt if there is enough oxygen supplied by the burner. But, primary carbon monoxide is from reaction gases is combusting. Finally, significant part of carbon goes to chimney being emitted to the atmosphere. According to invention, floating bed of charcoal or coke on the copper surface acts as a filter for the carbon particles. The particles are caught by a filter, sintered and the carbon is used as a reductant together with charcoal. This leads to higher utilisation of carbon and higher reductant efficiency. This invention has following advantages compared with traditional methods of copper reduction: a) Application of solid carbon addition combined with bath stirring by nitrogen introduced by porous plugs during injection of liquid or gaseous reductant significantly shorten reduction time from 40 to 60% in comparison to common reduction practice. b) Efficiency of reductant (carbon and hydrocarbons) increases from 30 to 50% of the average values of traditional operation. c) Emission of gases with black fumes (carbon black) is drastically decreased reducing negative process impact on the environment. d) Higher reductant efficiency and shorter reduction time results in the decrease of unitary reductant and fuel consumption as well as in the increase of furnace productivity, e) Cost of method application is low. Necessary modifications of refining furnace are minor. f) EXAMPLE 1
Copper refining is carried out in vascular anode furnace capacity of 150 t of copper as it is schematically illustrated in Figure 1.. Four porous plugs (2) are mounted in the bottom part of the furnace. Through the porous plugs nitrogen (1) is injected into the molten copper (4). Nitrogen flowrate varies from 40 to 120 NmVh. Oxidation period is ended by skimming out of the slag. Oxygen content in the copper is in the level of 8000 ppm. Next, 1.5 to 4 kg of charcoal (5) per tonne of copper is charged through the mouth onto copper surface. Flow of oil through one tuyere is put on (about 4 - 8 kg/h per tonne of copper) together with air (4 - 8 Nm3/h per tonne of copper). Furnace is tilted and the tuyere immersed starting to blow into the copper. Oil flowrate is increased gradually up to the point that black fumes are not emitted. Setting of the burner is changed. Oil flowrate through the burner is shut down and air flow is kept at the level of 3 - 20 Nm3/h per tonne of copper. Introduced air through the burner ensures effective post-combustion of reduction gases leaving the bath. Charcoal on the surface prevents the copper against oxidation. Produced off-gases leaving the furnace to a chimney are clean and acceptable for emission. After 45 min of reductant injection through the tuyere oil flowrate is put gradually down and the furnace is tilted putting tuyere above the bath. Next, oil and air flow is shut down. Oxygen content in copper is 400 - 800 ppm and the furnace is prepared for anode casting.
EXAMPLE 2
Copper refining is carried out in stationary anode furnace of capacity 300 t of copper. Four porous plugs are installed in the bottom part of side wall against the wall with charging window. Nitrogen flowrate through porous plug is 0.3 - 1.0 NmVh per tonne of copper. After finishing oxidation period and skimming out of refining slag the portion of 1.3 - 4.0 kg of charcoal per tonne of copper is charged through a window onto the copper surface. Next, the oil flow is put on through a lance (2 - 5 kg/h per tonne of copper) together with air (2 - 5 Nm3/h tonne of copper). Lance is immersed into the copper and reduction. Burner is supplied by natural gas. Burner parameters are set: 1 - 3 Nm3/h of natural gas and 7 - 20 NmVh of air per tonne of copper. It ensures effective post-combustion of reduction gases and emission of clean off-gas to the atmosphere. After 100 min the lance is removed and the oil and air flows shut down. Oxygen content has been decreased from 6000 - 8000 ppm to about 400 - 800 ppm. Next, anode casting is proceeded.

Claims

Claims:
1. An installation for continuous copper fire refining, said the system of reactors comprising the components:
(a) launder transferring liquid blister copper from continuous converting furnace or from retention furnace into the first oxidation reactor;
(b) copper oxidation reactor;
(c) optionally settler separating oxidized copper and slag;
(d) launder transferring oxidized copper from oxidation reactor into reduction reactor;
(e) copper reduction reactor;
(f) launder transferring reduced copper from reduction reactor to casting will or to retention-casting furnace;
2. A method as said forth in claim 1, said the flow of liquid copper is gravitational and continuous through oxidation reactor and reduction reactor.
3. A method as said forth in claim 1, wherein in step (b) said oxidation reactor is a vertical, cylindrical or rectangular furnace made of steel shell and refractories, equipped with tuyeres injecting air or the mix of fuel and air. The furnace has siphon or inclined tapping hole for continuous evacuation of oxidized copper and tapping hole for continuous tapping out of refining slag. The furnace is filled by packed bed of ceramic grains, or another chemically neutral grains, size of 2 - 100 mm in diameter.
4. A method as said forth in claim 1 and claim 3, said the oxidation furnace is equipped with bean and charging system for fluxes addition and system of reaction gases evacuation to the stack.
5. A method as said forth in claim 1 and claim 3, said oxidized copper and slag flows downwards creating after phase separation two layers on the furnace hearth. Slag and copper are evacuated through siphon and tapping hole. Optionally, the oxidized copper can be tapped out together and the separation can be carried out in a launder-settler. A method as said forth in claim 1, wherein in step (e) said reduction furnace is a vertical, cylindrical or rectangular furnace made of steel shell and refractories, equipped with tuyeres injecting air or the mix of fuel and air. The furnace has siphon or inclined tapping hole for continuous evacuation of reduced copper. The furnace is filled by packed bed of charcoal grains, or coke grains of low sulphur content, size of 2 - 100 mm in diameter.
PCT/US2005/031945 2004-09-07 2005-09-06 Installation for continuous fire refining of copper Ceased WO2006029246A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
MX2007002782A MX2007002782A (en) 2004-09-07 2005-09-06 Installation for continuous fire refining of copper.
EP05794326A EP2111471A4 (en) 2004-09-07 2005-09-06 APPARATUS FOR CONTINUOUS FIRE REFINING OF ZINC
CA2579586A CA2579586C (en) 2004-09-07 2005-09-06 Installation for continuous fire refining of copper
AU2005282368A AU2005282368B2 (en) 2004-09-07 2005-09-06 Installation for continuous fire refining of copper

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CL2270 2004-09-07
CL2004002270 2004-09-07

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EP (1) EP2111471A4 (en)
KR (1) KR20080099119A (en)
AU (1) AU2005282368B2 (en)
CA (1) CA2579586C (en)
MX (1) MX2007002782A (en)
WO (1) WO2006029246A1 (en)

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WO2009077851A1 (en) * 2007-12-19 2009-06-25 Universidad De Chile Continuous fire reduction of liquid copper
CN105039738A (en) * 2015-07-27 2015-11-11 王泊远 Crude copper fire refining furnace and process
CN109897972A (en) * 2019-03-29 2019-06-18 东营方圆有色金属有限公司 A kind of short route copper smelting method suitable for middle and small scale
CN115109945A (en) * 2022-06-30 2022-09-27 金川集团股份有限公司 Impurity removal method for PS copper converter
CN116287760A (en) * 2023-03-24 2023-06-23 长沙有色冶金设计研究院有限公司 Blister copper continuous refining method and device

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WO2015077900A1 (en) 2013-11-28 2015-06-04 Gabriel Angel Riveros Urzúa Method for the continuous processing of copper matte or copper-nickel matte
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WO2009077851A1 (en) * 2007-12-19 2009-06-25 Universidad De Chile Continuous fire reduction of liquid copper
AU2008337224B2 (en) * 2007-12-19 2013-08-01 Empresa Nacional De Mineria Continuous fire reduction of liquid copper
US8801830B2 (en) 2007-12-19 2014-08-12 Universidad De Chile Continuous fire reduction of liquid copper
CN105039738A (en) * 2015-07-27 2015-11-11 王泊远 Crude copper fire refining furnace and process
CN109897972A (en) * 2019-03-29 2019-06-18 东营方圆有色金属有限公司 A kind of short route copper smelting method suitable for middle and small scale
CN109897972B (en) * 2019-03-29 2021-07-16 东营方圆有色金属有限公司 A short process copper smelting method suitable for small and medium scale
CN115109945A (en) * 2022-06-30 2022-09-27 金川集团股份有限公司 Impurity removal method for PS copper converter
CN116287760A (en) * 2023-03-24 2023-06-23 长沙有色冶金设计研究院有限公司 Blister copper continuous refining method and device

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CA2579586C (en) 2017-06-13
EP2111471A1 (en) 2009-10-28
MX2007002782A (en) 2009-02-12
EP2111471A4 (en) 2009-10-28
KR20080099119A (en) 2008-11-12
CA2579586A1 (en) 2006-03-16
AU2005282368B2 (en) 2011-04-21

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