[go: up one dir, main page]

US2111575A - Refining of nonferrous metals - Google Patents

Refining of nonferrous metals Download PDF

Info

Publication number
US2111575A
US2111575A US91298A US9129836A US2111575A US 2111575 A US2111575 A US 2111575A US 91298 A US91298 A US 91298A US 9129836 A US9129836 A US 9129836A US 2111575 A US2111575 A US 2111575A
Authority
US
United States
Prior art keywords
copper
tin
lead
electrolyte
ribbon
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
US91298A
Inventor
James R Stack
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.)
Nassau Smelting & Refining Com
Nassau Smelting & Refining Company Inc
Original Assignee
Nassau Smelting & Refining Com
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 Nassau Smelting & Refining Com filed Critical Nassau Smelting & Refining Com
Priority to US91298A priority Critical patent/US2111575A/en
Application granted granted Critical
Publication of US2111575A publication Critical patent/US2111575A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25CPROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C1/00Electrolytic production, recovery or refining of metals by electrolysis of solutions
    • C25C1/12Electrolytic production, recovery or refining of metals by electrolysis of solutions of copper

Definitions

  • the guide member 5'! is mounted in cylindrical bushings 85 which are carried in brackets 86 on the supporting frame 81.
  • the guide 5i may be given a rotary movement by adjusting the set screws 88 and 89 and its Vertical position may be adjusted by the set screws. 98 and bl. These adjustments are provided so that the guide 57 can be positioned to receive the ribbon from diiferent sizes of feed rolls and also so that it can be adjusted to properly deliver the ribbon to the guide roll 58 and, the bending pins BI and 63.”
  • the guide roll 58 is mounted on a vertical shaft 92 which fits within a sleeve 93.
  • the vertical position of the sleeve 93 and the shaft 92 can be regulated by the screws 94 and 95, screw 94 having threaded engagement with the frame and screw 95 'being adapted to abut against the frame.
  • the ribbon is for'med'slightly thinner on one edge than on the otherand the reel is: so arranged that the thin edge of the ribbon is toward the front as is seen in Figure 1.
  • and 2'! may be contoured to fit this tapered section ribbon and the top roll 21 is provided with a flange 21' (Fig. 2) to prevent the ribbon from running off the rolls.
  • the desired frictional engagement is obtained between the ribbon and the rolls by the action of the adjustable weightlfl on the lever arm! 5.
  • the maximum driving effort can be produced with a minimum pressure on the ribbon and in this way the ribbon can be fed without distorting its cross-sectional dimensions.
  • the ribbon passes through the guide 51
  • the end of the ribbon is bent by hand around the guide roll 58, past the primary bending pin 6! and between the secondary bending pin 65 and the inner end of the groove 63' in the bar 63.
  • the motor 46 may be started and the ribbon will be fed by the .feed rollsand bent by the pins 6! and 55 into a ring of accurate diameter.
  • the feed rolls will stop and the cut-off knives will act to sever the ring.
  • the feed rolls willthen again start and feed through the machine a length of ribbon sufficient to form one complete ring.
  • the machine will again stop and the cut-off operation will be repeated. This cycle will be continued until the roll of ribbon is exhausted or the driving motor is stopped.
  • the resulting ring By forming the ribbon slightly thinner on the inside edge than on the outside edge the resulting ring will be of uniform thickness across its entire width. This is due to the thickening of the metal on the inside of the neutral axis of the ring due to the compression which takes place during the forming operation and the reduction in thickness at the outside due to the tensile force exerted thereon.
  • the finished rings By supplying a properly shaped ribbon the finished rings will be of substantially uniform thickness and, due to my improved forming method, each ring will be of uniform diameter within'very close limits. regardless of variations in the characteristics of the ribbon, etc.
  • the method of forming a ring from a metal wire or the like which includes the steps of moving the ribbon in the direction of its length, imposing a primary bending force on the moving ribbon whereby the moving ribbon will be bent to form a ring, imposing a second bending force on said moving ribbon opposite to said primary force whereby the ribbon will assume a ring form of diameter different from that of the primary bend.
  • the method of forming a ring of wire or the like which includes the steps of moving the wire in the direction of its length, bending the moving wire to form a ring, and then, while continuing said bending of the moving wire, re-bending the moving 'wire to form a ring of different diameter, said re-bending being in a direction opposite tothe first bending.
  • the method of forming a metal ribbon or the like into ring form which includes the steps of first bending the ribbon to form a ring of one diameter and then re-bending the ribbon to form a ring of another diameter, said re-bending being effected on one part of the ribbon while the first bending is being effected on another part of the ribbon and before a complete ring has been formed by said first bending.
  • the method of forming rings of metal ribbon, wire or the like which includes the steps of moving the ribbon in the direction of its length, bending the moving ribbon to form a ring of a predetermined diameter, and re-bending the moving ribbon, at a point adjacent said first bending while continuin'g said first bending, to
  • This invention relates to the refining of nonferrous metals andv more particularly to the refining of copper bearing materials.
  • the impure material is charged into a blast furnace and smelted to remove the major portion of the iron.
  • the metal obtained from the blast furnace is transferred to a converter and substantially all of the lead, zinc and tin are removed by blowing with air.
  • copper matte or leady copper matte is added to the converter charge to assist in the removal of lead and tin.
  • the resulting fumes are collected in a bag house in the form of a dust or fume and the latter material is treated to separate the metals or compounds contained therein.
  • the remaining metal is transferred to a reverberatory furnace and is further refined by blowing and poling, after which -it is cast into anodes which are electrolytically refined in a standard sulphuric acid electrolyte.
  • the principal objections to this process are that the metal must be carried through a number of refining steps in order to obtain pure copper and the bag house dust or fume containing the lead, tin and zinc is difilcult to treat to recover the constituent metals.
  • the scrap material is treated in a blast furnace to eliminate the iron and the resultant molten metal is charged into a converter where substantially all of the zinc only is removed by blowing with air.
  • the metal from the converter is cast into anodes and is electrolyzed for the production of copper in a sulphuric acid electrolyte of relatively low concentration.
  • the metals other than copper such as lead and tin
  • Any dissolved antimony is rendered insoluble as any oxychloride by the presence of chlorine ions, previously added to the solution, or by other known means.
  • anode slimes produced are treated to recover the metallic'values therein.
  • objections to this process are the high cost of the electrolytic refining due to the abnormally high cell voltage necessitated by the low conductivity of the electrolyte and the large amount of slimes produced. Furthermore, it is very diflicult to treat these slimes to separate and recover the various metals contained therein. These slimes also interfere with the operation of the cell and in addition carry considerable quantities of copper down with them.
  • a further object of the invention is to provide new and improved electrolytes for use in the aforesaid electrolytic refining processes.
  • the material 'to be refined is smelted in a blast furnace in the usual manner to remove the iron therefrom and the metal obtained from the blast furnace is transferred to a converter where substantially all of the zinc, but as little lead and tin as possible, is removed by blowing with air.
  • the zinc fumes from the blast furnace and the converter are conveyed to a bag house and collected in the form of dust.
  • the blown converter metal is cast into anodes which are electrolyzed for the production of pure copper cathodes in an electrolyte in which lead, tin and copper are all soluble. Since both lead and tin are more electropositive than copper, they will not be deposited upon the cathode but will be dissolved and remain in the electrolyte.
  • the solution is then removed to a separate container where the remainder of the copper is removed by cementation, by means of lead, tin, or a mixture thereof preferably in slab form.
  • the copper precipitates out, and the electrolyte is separated from the free copper by decantation or in any other convenient manner.
  • the copper free electrolyte which consists essentially of a solution of lead and tin, may then be electrolyzed and. since lead and tin are close together in the electromotive series, these metals will deposit simultaneously as a lead-tin alloy at the cathode. If the tin content of the resulting I alloy is sufliciently high, the alloy may be used directly as -a solder and in this case the cathodes are melted andcast into solder bars.
  • some or all of the lead may be removed before electrolysis by precipitating it out by means of a suitable reagent, such as sulphuric'acid, added in a quantity just sufficient to react with the quantity of lead which it is desired to remove.
  • a suitable reagent such as sulphuric'acid
  • an anode consisting of a lead electrode surrounded by a porous diaphragm cell is preferably employed.
  • An anode of this type is used to prevent dissolving of the anode, which would alter the composition of the deposit, and to prevent oxidation of the tin to the stannic form which will not deposit readily.
  • anchthe bath is preferably heated to a temperature of, 100 to 150 F. by any suitable means. 1 *2 It is not essential that the lead and tin be removed from the copper-free electrolyte by electrodeposition, and they may, if desired, be separated by purely chemical methods.
  • the lead may be precipitated as a sulphate and after removal of the resulting precipitate the tin may be removed as an insoluble stannate.
  • the products obtained may be used or disposed of in their precipitated forms, or may be further treated to obtain other useful compounds or the metals lead and tin therefrom.
  • the lead and tin After the lead and tin have been removed from the solution, either by electrolysis or by chemical means, the latter is transferred to an evaporator and concentrated to a point where any salts of such metals as zinc, iron and nickel contained therein will crystalize out. These crystals are removed from the concentrated solution by any suitable filtering apparatus and the concentrated solution is employed to make up fresh electrolyte. If desired, some or all of the solution may be reused after the removal of the lead and tin withouthaving the compounds of zinc, iron, nickel and similar metals removed.
  • the aromatic .sulphonic acids are preferably used in the electrolyte in carrying out the electrolytic steps in the refining process embodying the invention for several reasons. In the first place, they dissolve not only the copper but also the lead and tin. In addition, they have a high conductivity, they are relatively non-volatile, and are not appreciably decomposed electrolytically. They, therefore, permit the electrolytic deposition of pure copper without the precipitation of substantial quantities of the lead and tin as slimes. Their high conductivity lowers the power consumption and their stability makes them economical to use because they may be recovered and reused.
  • aromatic sulphonic acids which may be employed are the mono and poly sulphonic acids of phenol, benzol (benzene), toluol (tolucue), the cresols, the xylenes, the xylenols, naphthalene, the naphthols, anthracene, phenanthrene, and related compounds.
  • the related chloro and nitro sulphonic acids of aromatic hydrocarbons may, likewise, be used.
  • the method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of copper and an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufficiently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
  • the method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of copper and an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids to dissolve the-copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sui'ficiently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte, removing a portion of the electrolyte when a substantial amount of lead and tin has accumulated therein and recovering the lead and tin from said portion.
  • the method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of copper and an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufiiciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte, removing a portion of the electrolyte when a substantial amount of lead and tin has accumulated therein, removing the copper from said portion and electrolyzing said portion to deposit the lead and tin therefrom as an alloy.
  • the method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electroiyzing the same in an electrolyte consisting of copper and an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sumciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte, withdrawing a portion of the electrolyte when a substantial amount of lead and tin has accumulated therein, removing the copper from said portion, chemically precipitating the lead from said portion and electrolyzing the remaining solution to deposit the tin therefrom electrolytically.
  • the method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of copper and an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufllciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte, withdrawing a portion of the electrolyte when a substantial amount of lead and tin has accumulated therein, removing the copper from said portion, chemically precipitating the tin from said portion and electrolyzing the remaining solution to deposit the lead therefrom electrolytically.
  • the method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electroiyzing the same in an electrolyte consisting of copper and an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufliciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte, withdrawing a portion of the electrolyte when a substantial amount of lead and tin has accumulated therein, removing the copper from said portion by successive electrolysis and cementation steps and recovering the lead and tin from the resulting solution.
  • the method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of about 20%, an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids and.
  • the method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode. and electrolyzing the same in an electrolyte consisting of copper and a sulphonic acid of benzene to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufllciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
  • the method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of copper and a sulphonic acid of phenol to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufliciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
  • the method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of copper and a sulphonic acid of cresol to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufiiciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
  • the method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of about 20% of a sulphonic acid of benzeneand about 3% of copper as a salt of said acid to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufficiently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
  • an electrolyte consisting of about 20% of a sulphonic acid of benzeneand about 3% of copper as a salt of said acid to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufficiently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the
  • the method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of about 20% of a sulphonic acid of phenol and about 3% of copper as a salt of said acid to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufliciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
  • an electrolyte consisting of about 20% of a sulphonic acid of phenol and about 3% of copper as a salt of said acid to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufliciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and
  • the method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of about 20% of a sulphonic acid of cresol and about 3% of copper as a salt of said acid to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufllciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electrolytic Production Of Metals (AREA)

Description

through the angular distance necessary to effect a complete stop and cut-off operation. As soon as the cut-off stroke is completed the latch 54 will be withdrawn from the notch 59 and the disc 36 and shaft 28 will be immediately picked up by the clutch and the stock feeding movement resumed.
It will be understood that by varying the sizes of the feed rolls 2| and 2?, rings of different diameter may be formed. The circumference of the rolls 2i and 21 should be substantially the same as the length of the ribbon making up a single ring. The position of the cut-off mechanism can be adjusted by moving the frame 12 and the cam 18 along the shaft 76. Likewise the position of the bending pins v6! and 65 can be adjustedby the micrometer screws in order to accommodate rings of a considerable range of sizes. A
As is seen in Figures 3 and 5 the guide member 5'! is mounted in cylindrical bushings 85 which are carried in brackets 86 on the supporting frame 81.. The guide 5i may be given a rotary movement by adjusting the set screws 88 and 89 and its Vertical position may be adjusted by the set screws. 98 and bl. These adjustments are provided so that the guide 57 can be positioned to receive the ribbon from diiferent sizes of feed rolls and also so that it can be adjusted to properly deliver the ribbon to the guide roll 58 and, the bending pins BI and 63."
As .is'seen in Figure '7 the guide roll 58 is mounted on a vertical shaft 92 which fits within a sleeve 93. The vertical position of the sleeve 93 and the shaft 92 can be regulated by the screws 94 and 95, screw 94 having threaded engagement with the frame and screw 95 'being adapted to abut against the frame.
In the operation of my improved ring forming machine it is merely necessary to place a reel of ribbon on the arm 3 and feed the ribbon up over the guide rolls 9 and I4 and between the feedrolls 2i and 21. Preferably the ribbon is for'med'slightly thinner on one edge than on the otherand the reel is: so arranged that the thin edge of the ribbon is toward the front as is seen in Figure 1. The surface of the feed rolls 2| and 2'! may be contoured to fit this tapered section ribbon and the top roll 21 is provided with a flange 21' (Fig. 2) to prevent the ribbon from running off the rolls. The desired frictional engagement is obtained between the ribbon and the rolls by the action of the adjustable weightlfl on the lever arm! 5. As both the top and bottom feed rolls 2| and 21 are driven the maximum driving effort can be produced with a minimum pressure on the ribbon and in this way the ribbon can be fed without distorting its cross-sectional dimensions. After it leaves the feed rolls the ribbon passes through the guide 51 In starting the machine in operation the end of the ribbon is bent by hand around the guide roll 58, past the primary bending pin 6! and between the secondary bending pin 65 and the inner end of the groove 63' in the bar 63. After this initial manual bending the motor 46 may be started and the ribbon will be fed by the .feed rollsand bent by the pins 6! and 55 into a ring of accurate diameter. As soon as a complete ring has been formed the feed rolls will stop and the cut-off knives will act to sever the ring. The feed rolls willthen again start and feed through the machine a length of ribbon sufficient to form one complete ring. When this hasbeen done the machine will again stop and the cut-off operation will be repeated. This cycle will be continued until the roll of ribbon is exhausted or the driving motor is stopped.
By forming the ribbon slightly thinner on the inside edge than on the outside edge the resulting ring will be of uniform thickness across its entire width. This is due to the thickening of the metal on the inside of the neutral axis of the ring due to the compression which takes place during the forming operation and the reduction in thickness at the outside due to the tensile force exerted thereon. By supplying a properly shaped ribbon the finished rings will be of substantially uniform thickness and, due to my improved forming method, each ring will be of uniform diameter within'very close limits. regardless of variations in the characteristics of the ribbon, etc.
Although I have described in considerable detail the illustrated embodiment of a machine for carrying out my improved method it will be understood by those skilled in the art that many variations and modifications may be made in the specific apparatus illustrated and described. Other'types of devices might be provided for bending and cutting off the ribbon in accordance with my improved method. I do.
not therefore wish to be limited to the specific form herein described and illustrated but claim as my invention. all embodiments thereof coming within the scope of the appended claims.
I claim:
1. The method of forming a ring from a metal wire or the like which includes the steps of moving the ribbon in the direction of its length, imposing a primary bending force on the moving ribbon whereby the moving ribbon will be bent to form a ring, imposing a second bending force on said moving ribbon opposite to said primary force whereby the ribbon will assume a ring form of diameter different from that of the primary bend.
2. The method of forming a ring of wire or the like which includes the steps of moving the wire in the .direction of its length, bending the moving wire to form a ring, and then'while continuing said bending of the moving wire, re-bending the moving wire to form a ring of different diameter, said re-bending taking place before a complete ring is formed. l i
3. The method of forming a ring of wire or the like which includes the steps of moving the wire in the direction of its length, bending the moving wire to form a ring, and then, while continuing said bending of the moving wire, re-bending the moving 'wire to form a ring of different diameter, said re-bending being in a direction opposite tothe first bending.
4. The method of forming a metal ribbon or the like into ring form which includes the steps of first bending the ribbon to form a ring of one diameter and then re-bending the ribbon to form a ring of another diameter, said re-bending being effected on one part of the ribbon while the first bending is being effected on another part of the ribbon and before a complete ring has been formed by said first bending.
5. The method of forming rings of metal ribbon, wire or the like which includes the steps of moving the ribbon in the direction of its length, bending the moving ribbon to form a ring of a predetermined diameter, and re-bending the moving ribbon, at a point adjacent said first bending while continuin'g said first bending, to
Patented Mar. 22, 1938 UNITED STATES PATENT. OFFICE REFINING F NONFERROUS METALS ration of New York Applicationluly 18, 1936, Serial No. 91,298
14 Claims.
This invention relates to the refining of nonferrous metals andv more particularly to the refining of copper bearing materials.
Considerable quantities of scrap materials containing substantial amounts of copper and lesser amounts of tin, lead, zinc, iron and other metals are obtained from discarded materials, such as used telephone and other electrical equipment, machine shop turnings, refinery and foundry scraps and materials from various other sources. Efforts have been made heretofore to refine these low grade materials to obtain the constituent metals therefrom in usable forms.
In one process which has been used heretofore, the impure material is charged into a blast furnace and smelted to remove the major portion of the iron. The metal obtained from the blast furnace is transferred to a converter and substantially all of the lead, zinc and tin are removed by blowing with air. In some instances copper matte or leady copper matte is added to the converter charge to assist in the removal of lead and tin. The resulting fumes are collected in a bag house in the form of a dust or fume and the latter material is treated to separate the metals or compounds contained therein. The remaining metal is transferred to a reverberatory furnace and is further refined by blowing and poling, after which -it is cast into anodes which are electrolytically refined in a standard sulphuric acid electrolyte. The principal objections to this process are that the metal must be carried through a number of refining steps in order to obtain pure copper and the bag house dust or fume containing the lead, tin and zinc is difilcult to treat to recover the constituent metals.
In another process which has been practiced previously, the scrap material is treated in a blast furnace to eliminate the iron and the resultant molten metal is charged into a converter where substantially all of the zinc only is removed by blowing with air. The metal from the converter is cast into anodes and is electrolyzed for the production of copper in a sulphuric acid electrolyte of relatively low concentration. During the electrolysis most of the metals other than copper, such as lead and tin, are converted into insoluble compounds, and some of these compounds adhere to the anodes, some remain suspended in the electrolyte and the balance fall to the bottom of the electrolytic cell in the form of anode slimes. Any dissolved antimony is rendered insoluble as any oxychloride by the presence of chlorine ions, previously added to the solution, or by other known means. The
anode slimes produced are treated to recover the metallic'values therein. Among the objections to this process are the high cost of the electrolytic refining due to the abnormally high cell voltage necessitated by the low conductivity of the electrolyte and the large amount of slimes produced. Furthermore, it is very diflicult to treat these slimes to separate and recover the various metals contained therein. These slimes also interfere with the operation of the cell and in addition carry considerable quantities of copper down with them.
Among the objects of the present invention are the provision of an effective and economical method of refining low grade copper bearing materials to obtain the principal constituents thereof in usable forms and the provision of electrolytic processes for separation of metals such as copper, lead and tin without the production of large amounts of slimes.
A further object of the invention is to provide new and improved electrolytes for use in the aforesaid electrolytic refining processes.
In accordance with one embodiment of the invention, the material 'to be refined is smelted in a blast furnace in the usual manner to remove the iron therefrom and the metal obtained from the blast furnace is transferred to a converter where substantially all of the zinc, but as little lead and tin as possible, is removed by blowing with air. The zinc fumes from the blast furnace and the converter are conveyed to a bag house and collected in the form of dust. The blown converter metal is cast into anodes which are electrolyzed for the production of pure copper cathodes in an electrolyte in which lead, tin and copper are all soluble. Since both lead and tin are more electropositive than copper, they will not be deposited upon the cathode but will be dissolved and remain in the electrolyte. When the quantity of lead and tin in the electrolyte has built up to the point where the copper will not be deposited in a sumciently' pure state, a portion of the electrolyte is removed, the copper content thereof is partially depleted by electrolysis with an insoluble anode, the remainder of the copper is thrown out of solution by replacement, and the lead and tin are subsequently recovered, preferably by electrolysis.
The above described and other objects and features of the invention will be more apparent from the following detailed description thereof taken in conjunction with the accompanying drawing in which is outlined a flow sheet of a process embodying the invention.
shaft from rotation, and means operated by said drive shaft for moving said latch pin out of locking position to permit rotation of said r011 shaft and roll.
30. In apparatus for forming rings from metallic ribbon or the like, means for feeding the ribbon in the direction of its length, primary bending means interposed in the path of the ribbon and adapted to deflect the ribbon sufficiently to cause it to take a. permanent set and be bent into ring form, and secondary ribbon bending means interposed in the path of the ribbon as it leaves said primary bending means, said secondary bending means being adapted to re-bend said ribbon into a ring of different diameter than that formed by said primary bending means.
DEAN M. SOLENBERGER.
the copper from the anodes during the electrolysis but, since they are both electropositive to copper and are not near copper in the electromotive series of metals, they will not deposit at the cathodes at the initial concentration of the electrolyte. Consequently, the lead and tin will remain in solution in the electrolyte while the copper is deposited in a pure state on the cathodes. It will be evident that in this process, more copper will deposit at the cathodes than will be dissolved from the anodes and in order to maintain the concentration of the bath at the desired value, this deficiency is made up by dissolving copper in the electrolyte externally of the electrolytic cell. This is preferably accomplished by circulating a portion of the electrolyte through oxidizer tanks containing particles of copper and by blowing air through the electrolyte in these tanks to render the copper more soluble, although the copper may be added in other ways.
During the electrolysis just described, a small amount of slimes will be produced which contain antimony and precious metals originally present in the anode, together with some copper and small amounts of lead, tin and other elements. These slimes are collected and treated for the removal of copper and the recovery of the precious metals contained therein.
In view of the fact that neither the lead nor the tin is deposited at the cathode, these metals will gradually increase in concentration in the electrolyte and will eventually render the electrolyte ineffective for the deposition of pure copper. Consequently, a portion of the solution is removed from time to time and the lead and tin present therein are removed. This portion of the electrolyte will, of course, contain copper in solution and the copper is removed therefrom in order to obtain the lead and tin unmixed with copper. This is preferably accomplished by first electrolyzing the solution, using an insoluble anode of a type well-known in the art, until a substantial portion of the copper is deposited out. The solution is then removed to a separate container where the remainder of the copper is removed by cementation, by means of lead, tin, or a mixture thereof preferably in slab form. Upon the addition of the replacement metal, the copper precipitates out, and the electrolyte is separated from the free copper by decantation or in any other convenient manner.
The copper free electrolyte, which consists essentially of a solution of lead and tin, may then be electrolyzed and. since lead and tin are close together in the electromotive series, these metals will deposit simultaneously as a lead-tin alloy at the cathode. If the tin content of the resulting I alloy is sufliciently high, the alloy may be used directly as -a solder and in this case the cathodes are melted andcast into solder bars. If it is desired to produce an alloy containing a higher quantity of tin or to obtain pure tin, some or all of the lead may be removed before electrolysis by precipitating it out by means of a suitable reagent, such as sulphuric'acid, added in a quantity just sufficient to react with the quantity of lead which it is desired to remove.
In the electrolysis involving the deposition of a lead-tin alloy, or of the tin alone, an anode consisting of a lead electrode surrounded by a porous diaphragm cell is preferably employed. An anode of this type is used to prevent dissolving of the anode, which would alter the composition of the deposit, and to prevent oxidation of the tin to the stannic form which will not deposit readily. A
current density of from 10 to amperes per squarefoot may be employed in this step of the process anchthe bath is preferably heated to a temperature of, 100 to 150 F. by any suitable means. 1 *2 It is not essential that the lead and tin be removed from the copper-free electrolyte by electrodeposition, and they may, if desired, be separated by purely chemical methods. For example, the lead may be precipitated as a sulphate and after removal of the resulting precipitate the tin may be removed as an insoluble stannate. The products obtained may be used or disposed of in their precipitated forms, or may be further treated to obtain other useful compounds or the metals lead and tin therefrom.
After the lead and tin have been removed from the solution, either by electrolysis or by chemical means, the latter is transferred to an evaporator and concentrated to a point where any salts of such metals as zinc, iron and nickel contained therein will crystalize out. These crystals are removed from the concentrated solution by any suitable filtering apparatus and the concentrated solution is employed to make up fresh electrolyte. If desired, some or all of the solution may be reused after the removal of the lead and tin withouthaving the compounds of zinc, iron, nickel and similar metals removed.
The various steps of the preferred process may be readily followed by means of the flow sheet outlined in the accompanying drawing. The principal steps of the process have been described I hereinabove and a few auxiliary, and more or less conventional, steps are indicated on the flow sheet. These latter are of such a nature as are well understood in the art, and a detailed description thereof is unnecessary for a complete understanding of the invention.
The aromatic .sulphonic acids are preferably used in the electrolyte in carrying out the electrolytic steps in the refining process embodying the invention for several reasons. In the first place, they dissolve not only the copper but also the lead and tin. In addition, they have a high conductivity, they are relatively non-volatile, and are not appreciably decomposed electrolytically. They, therefore, permit the electrolytic deposition of pure copper without the precipitation of substantial quantities of the lead and tin as slimes. Their high conductivity lowers the power consumption and their stability makes them economical to use because they may be recovered and reused.
Among the aromatic sulphonic acids which may be employed are the mono and poly sulphonic acids of phenol, benzol (benzene), toluol (tolucue), the cresols, the xylenes, the xylenols, naphthalene, the naphthols, anthracene, phenanthrene, and related compounds. The related chloro and nitro sulphonic acids of aromatic hydrocarbons may, likewise, be used. In addition,
satisfactory results may be obtained by using invention to employ any acid which forms soluble salts of copper, lead and tin and which has sufiicient conductivity to render it an effective electrolyte.
Since the acids mentioned above dissolve copper, lead and tin, it is obvious that the invention may be practised to refine copper bearing metals that include either one or both of lead and tin. For example, scrap brasses may contain no tin, while bronzes may be free from lead. These materials may be carried through the refining steps described in the same manner that is employed for materials containing both lead and tin, the only difierence being that the products obtained would not include lead or tin, as the case may be.
From the foregoing description, it is apparent that the invention provides simple, effective and economical processes for refining non-ferrous metals. It also provides new and improved electrolytes and electrolytic processes for the separation of metals, including copper, lead and tin. Various modifications and changes may, of course, be made to adapt the invention to varying conditions. Hence, the invention is not limited to the specific embodiments described herein, but embraces all modifications and equivalents falling within the scope of the annexed claims.
What is claimed is:
1. The method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of copper and an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufficiently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
2. The method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of copper and an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids to dissolve the-copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sui'ficiently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte, removing a portion of the electrolyte when a substantial amount of lead and tin has accumulated therein and recovering the lead and tin from said portion.
3. The method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of copper and an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufiiciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte, removing a portion of the electrolyte when a substantial amount of lead and tin has accumulated therein, removing the copper from said portion and electrolyzing said portion to deposit the lead and tin therefrom as an alloy.
4. The method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electroiyzing the same in an electrolyte consisting of copper and an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sumciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte, withdrawing a portion of the electrolyte when a substantial amount of lead and tin has accumulated therein, removing the copper from said portion, chemically precipitating the lead from said portion and electrolyzing the remaining solution to deposit the tin therefrom electrolytically.
5. The method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of copper and an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufllciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte, withdrawing a portion of the electrolyte when a substantial amount of lead and tin has accumulated therein, removing the copper from said portion, chemically precipitating the tin from said portion and electrolyzing the remaining solution to deposit the lead therefrom electrolytically.
6. The method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electroiyzing the same in an electrolyte consisting of copper and an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufliciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte, withdrawing a portion of the electrolyte when a substantial amount of lead and tin has accumulated therein, removing the copper from said portion by successive electrolysis and cementation steps and recovering the lead and tin from the resulting solution.
7. The method of refining metallic materials consisting essentially of copper with small amounts of iron, zinc, lead and tin which comprises smelting the materials and blowing the smelted material with air to separate the iron and zinc and to leave a metal consisting essentially of copper with small amounts of lead and tin, making the latter metal into an anode and electrolyzing the same in an electrolyte consisting of copper and an acid of the group consisting of benzene sulphonic acid, phenol sulphonic acid, cresol sulphonic acid and the corresponding chloro and nitro sulphonic acids to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electro lyte substantially constant and sufliciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
8. The method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of about 20%, an acid of the group consisting of the mono and poly sulphonic acids of benzene, phenol and cresol and the related chloro and nitro sulphonic acids and.
' about 3% of copper as a salt of said acid to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufiiciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
9. The method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode. and electrolyzing the same in an electrolyte consisting of copper and a sulphonic acid of benzene to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufllciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
10. The method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of copper and a sulphonic acid of phenol to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufliciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
11. The method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of copper and a sulphonic acid of cresol to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufiiciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
12. The method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of about 20% of a sulphonic acid of benzeneand about 3% of copper as a salt of said acid to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufficiently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
13. The method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of about 20% of a sulphonic acid of phenol and about 3% of copper as a salt of said acid to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufliciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.
14. The method of refining metallic materials containing principally copper and small amounts of lead and tin which comprises making such material into an anode and electrolyzing the same in an electrolyte consisting of about 20% of a sulphonic acid of cresol and about 3% of copper as a salt of said acid to dissolve the copper, lead and tin anodically while maintaining the copper concentration of the electrolyte substantially constant and sufllciently high so that only copper deposits at the cathode while the lead and tin build up in the electrolyte and subsequently recovering the lead and tin from the electrolyte.-
JAMES R. STACK.
US91298A 1936-07-18 1936-07-18 Refining of nonferrous metals Expired - Lifetime US2111575A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US91298A US2111575A (en) 1936-07-18 1936-07-18 Refining of nonferrous metals

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US91298A US2111575A (en) 1936-07-18 1936-07-18 Refining of nonferrous metals

Publications (1)

Publication Number Publication Date
US2111575A true US2111575A (en) 1938-03-22

Family

ID=22227061

Family Applications (1)

Application Number Title Priority Date Filing Date
US91298A Expired - Lifetime US2111575A (en) 1936-07-18 1936-07-18 Refining of nonferrous metals

Country Status (1)

Country Link
US (1) US2111575A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2461350A (en) * 1943-11-06 1949-02-08 Cleveland Graphite Bronze Co Electrodeposition of leadantimony-tin alloys
US2525943A (en) * 1947-09-24 1950-10-17 Standard Oil Co Copper plating bath and process
US2576362A (en) * 1947-10-08 1951-11-27 Westinghouse Electric Corp Electrophoretic method of coating wire with graphite
US3148130A (en) * 1961-05-12 1964-09-08 Banner Mining Company Recovery of copper sponge from oxidized copper ores
US3194653A (en) * 1963-05-06 1965-07-13 Harmon E Keyes Copper recovery process
USH970H (en) 1989-06-08 1991-10-01 The United States Of America As Represented By The United States Department Of Energy Integrated decontamination process for metals

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2461350A (en) * 1943-11-06 1949-02-08 Cleveland Graphite Bronze Co Electrodeposition of leadantimony-tin alloys
US2525943A (en) * 1947-09-24 1950-10-17 Standard Oil Co Copper plating bath and process
US2576362A (en) * 1947-10-08 1951-11-27 Westinghouse Electric Corp Electrophoretic method of coating wire with graphite
US3148130A (en) * 1961-05-12 1964-09-08 Banner Mining Company Recovery of copper sponge from oxidized copper ores
US3194653A (en) * 1963-05-06 1965-07-13 Harmon E Keyes Copper recovery process
USH970H (en) 1989-06-08 1991-10-01 The United States Of America As Represented By The United States Department Of Energy Integrated decontamination process for metals

Similar Documents

Publication Publication Date Title
CN112119182B (en) Improvements in copper electrorefining
US1911604A (en) Electrolytic process for the recovery of lead from waste materials
US2111575A (en) Refining of nonferrous metals
US3960681A (en) Method for producing electrolytic high purity lead using large-sized electrodes
US4030990A (en) Process for recovering electrolytic copper of high purity by means of reduction electrolysis
US5372684A (en) Process for the direct electrochemical refining of copper scrap
US2742415A (en) Electrodeposition of arsenic from acid electrolytes
EP0638667B1 (en) Process for continuous electrochemical lead refining
US4175027A (en) Apparatus for recovering zinc from residues
US2119936A (en) Method of recovering pure copper from scrap and residues
US3755112A (en) Electrowinning of copper
US3915818A (en) Electrowinning process for the improved recovery of metal
US3054736A (en) Method and apparatus for recovery of copper and zinc from scrap
US2286240A (en) Refining of nonferrous metals
US2294053A (en) Refining of nonferrous metals
US11280011B2 (en) Electrolytic method for extracting tin and/or lead contained in an electrically conductive mixture
US4104132A (en) Method for eliminating solution-level attack on cathodes during electrolysis
US2200139A (en) Process for recovery of metals from alloys and metallurgical residues
Fink et al. The Preparation of Pure Electrolytic Nickel: Part Two. The Final Elimination of Copper and the Removal of Cobalt and Iron
US1842028A (en) Method of recovering lead-tin alloys
US2361013A (en) Electrolytic refining of copperbearing materials
US1620580A (en) Metallurgy of tin
US2094632A (en) Metallurgical process
US2225904A (en) Lead oxide and electrolytic process of forming the same
US2011882A (en) Treating sulphate solutions of thallium and cadmium