US3484280A - Atmosphere control in dip-forming process - Google Patents

Atmosphere control in dip-forming process Download PDF

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US3484280A
US3484280A US628356A US3484280DA US3484280A US 3484280 A US3484280 A US 3484280A US 628356 A US628356 A US 628356A US 3484280D A US3484280D A US 3484280DA US 3484280 A US3484280 A US 3484280A
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copper
hydrogen
atmosphere
crucible
molten
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Roland P Carreker Jr
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General Electric Co
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    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/34Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the shape of the material to be treated
    • C23C2/36Elongated material
    • C23C2/38Wires; Tubes

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  • an elongated body such as a metal rod is typically pretreated by passing it through a straightener, a surface cleaning apparatus, and then through a vacuum entrance chamber positioned below or at the bottom of a crucible containing a bath of molten material.
  • a continuous elongated core or body is passed upwardly through the molten bath, which bath may have the same chemical composition as that of the core or a different composition.
  • the molten material in the crucible accretes or deposits upon the outer surface of the core thereby increasing its crosssectional area appreciably.
  • the resulting cast member After emerging from the crucible, the resulting cast member is cooled as by a water spray from one or more jet nozzles at least sufficiently so that the cast member can be rolled or worked. From there, the cast member may be passed through a suitable roll mechanism where it is reduced in cross-sectional area and then passed to a suitable receiving means such as a take-up reel.
  • the quality of the copper rod cast by the dip-forming process is influenced to a large extent by the gases dissolved in the molten copper, which are dependent upon the composition of the atmosphere in contact with the molten metal.
  • gas evolution results from the presence of excessive oxygen and/or hydrogen in the melt.
  • the problem of gas contamination in the dipforming process has been previously recognized, and in one aspect formed the basis of U.S. Patent No. 3,060,053 to Carreker and Parke and assigned to the assignee of this invention.
  • oxygen and hydrogen present in the atmosphere above the molten-metal can be dissolved by and/ or react with the motlen material. Oxygen may cause the formation of undesirable oxides. It is recognized that copper having an oxygen content greater than approximately 20 parts per million results in progressive deterioration in casting quality. Also, the presence of hydrogen alone, or hydrogen and oxygen concurrently, in molten metal in sufficient amounts will cause formation of gas bubbles upon solidifcation of the accreted material on the cast member.
  • oxides, gas bubbles and/ or voids not only adversely affects the quality of the product, but also deleteriously affects the uniform accretion of molten material onto the core by creating regions of relatively poor thermal conductivity within a mass of relatively good thermal conductivity.
  • oxygen and hydrogen is not confined to the oxide phases and bubbles they create,
  • Bubbles, voids, oxide phases, internal discontinuities, and irregular accretion are all undesirable in that they promote or cause the formation of cracks and fissures when stresses are imposed, as by bending, rolling, drawing or the like. A product manifesting such defects is generally not acceptable.
  • the oxygen content in the molten metal is reduced to a very low amount by utilizing graphite or comparable reducing means which will unite with the oxygen in the molten metal to form a gaseous product which escapes from the molten copper.
  • an inert atmosphere such as nitrogen is maintained above the surface of the melt to protect the melt from the air.
  • Such a furnace system will produce satisfactorily low oxygen content copper for use with dip-forming, if the furnace system is free of substantial air leaks and is allowed to come to substantial equilibrium.
  • air leaks may be expected in a large industrial furnace, particularly under charging conditions, and long residence times for equilibration are not realized.
  • Carbon monoxide is another reducing gas, but it is insoluble in molten copper and can react with the melt only at its surface. Therefore, carbon monoxide is relatively slow in reducing the oxygen content in a relatively deep melt. Further, strongly reducing atmospheres harmfully affect silicon carbide heating elements in that such atmospheres cause the formation of volatile silicon monoxide, which results in the eventual distintegration of the heating element.
  • the purpose of this invention is to provide a controlled reducing atmosphere above the molten copper which is sufficiently reducing to maintain the oxygen in the molten copper at less than approximately 20 parts per million, yet sufficiently oxidizing to avoid substantial erosion or attack of silicon carbide furnace elements employed in the system, and sufiiciently low in hydrogen to avoid evolution of hydrogen bubbles during solidification in the dip-forming process.
  • molten copper from a melting furnace is supplied to a crucible through which a continuous, elongated core rod is passed, whereby molten metal deposits or accretes to the rod.
  • a reducing atmosphere comprising 1 to 10 percent by volume hydrogen, 1 to 10 percent carbon monoxide, carbon dioxide, the ratio of carbon dioxide to carbon monoxide being from about 2:1 to 1:20, and the balance being an inert diluent such as nitrogen is maintained above the molten metal.
  • FIGURE 1 is a perspective view partially in section of an apparatus for practicing the present invention.
  • FIGURE 2 is a graph showing the solubility of hydrogen in copper.
  • core rod is supplied to a drawing apparatus 12 located adjacent a suitable shaving apparatus 14 which shaves a thin layer of metal from the periphery of the rod to remove the oxide coating and other surface contaminants therefrom.
  • a suitable shaving apparatus 14 which shaves a thin layer of metal from the periphery of the rod to remove the oxide coating and other surface contaminants therefrom.
  • other cleaning means such as chemical cleaning means, may be utilized for removing the oxide coating and cleaning the surface of the rod.
  • the rod is passed through a suitable drive means, including capstan 15 and drive rolls 16 contained in housing 18, and from there into tube 20.
  • Members 12, 14, 18 and 20 are sealed and interconnected to a suitable passageway, and tube 20 has connected thereto exhaust tube 22 and evacuating pump 24 to maintain a vacuum in the passageway.
  • Entry port member or nozzle 26 is mounted in the upper end of tube 20 and extends into crucible 28 which is maintained at the desired elevated temperature by suitable heating means such as electric induction heater 30.
  • Core lrod 10 is fed through nozzle 2-6 and into crucible 28 Where the rod comes into contact with the molten copper which accretes to the rod, as described hereinafter in greater detail.
  • Molten copper is supplied to crucible 28 from melting ifurnace indicated generally by the numeral 32, which is heated by a plurality of silicon carbide electric radiant heaters 34.
  • Cathode copper plates 35, or other suitable feed material of low oxygen content, is supplied to the furnace 32 by any suitable means such as a mechanical drive means (not shown).
  • the furnace is provided with a sloping or inclined section 36 and an integral horizontal section 38.
  • the cathode copper plates are charged to section 36 of the furnace through a dapper-type door (not shown) and melted gradually on the incline as they pass to the horizontal section 38 where a pool of molten metal collects.
  • the molten metal flows by displacement over a Weir 40 into a level control section 42 of the furnace.
  • a suitable liquid level sensing control indicated generally by the reference numeral 44, which is com- -monly employed in the art, controls subsurface flow through passageway 45 into dip-forming crucible 28.
  • An electric probe 46 in the crucible senses the bath level and automatically regulates the level sensing control to maintain a constant level in the crucible.
  • Copper supplied to the furnace may contain an undesirably high oxygen content, or air may leak to the furnace such as through the entranceway to the furnace through which the copper is charged. For this reason, it is necessary to maintain a controlled reducing atmosphere above the molten metal.
  • the reducing atmosphere is supplied to the furnace through line 48 from a suitable source (not shown).
  • the reducingr atmosphere lowers the oxygen content of the copper to less than 20 parts per million and maintains this low level.
  • the molten copper fed to the dip-forming crucible has this low oxygen content, and further does not contain sufficient hydrogen to cause hydrogen bubble formation during soliditication.
  • an atmosphere of an inert gas such as nitrogen is maintained above the molten metal in the crucible which may be supplied to the crucible through line 49 from source 50.
  • an inert gas such as nitrogen
  • An elongated tube 52 extends upwardly from crucible 28, and the resulting cast rod having copper accreted thereto is passed out of the crucible to the extension tube.
  • the cast rod emerging from the crucible and extension tube is at a relatively high temperature and is cooled somewhat by cooling means 54, such as a water spray nozzle, before the rod is passed through direction changing rolls 56. From there the cast rod is directed to a suitable rolling mill and coiling apparatus (not shown) and to a storage area as desired.
  • cooling means 54 such as a water spray nozzle
  • the reducing atmosphere supplied to the furnace comprises about 1 to 10 percent by volume hydrogen, 1 to 10 percent by volume carbon monoxide, carbon dioxide, the ratio of carbon dioxide to carbon monoxide being from about 2:1 to 1:20, and the balance being nitrogen or another suitable inert diluent.
  • the reducing gases of the atmosphere that is, the hydrogen and carbon monoxide, react with the oxygen present in the molten metal thereby reducing the oxygen content to less than 2() parts per million.
  • the oxidizing tendency of the atmosphere at a given temperature is specified by the ratio of carbon dioxide to carbon monoxide or by the ratio of water vapor to hydrogen; specifying either one of these ratios specifies the other, at equilibrium, according to the chemical Equation 1 Coz-l-HzCO +H2O 1
  • Equation 2 The oxygen content of the molten copper, at equilibrium is governed by Equation 2.
  • Equation 6 K2[O2]1/2 (4) per million is related to the ratio of CO2 to CO in the atmosphere by Equation 6.
  • the oxygen content of the molten copper in parts per million may be said to be about ten times the ratio of per cent carbon dioxide to percent carbon monoxide in the atmosphere, at equilibrium.
  • the presence of hydrogen offers more complete assurance against oxidation.
  • Hydrogen is soluble in molten copper, and the amount dissolved is related to the hydrogen content in the atmosphere above the molten metal and to the temperature.
  • Solid copper at its melting point of 1083o C. can retain up to 1.7 parts per million of hydrgen in solid solution in equilibrium with a hydrogen pressure of 1.0 atmosphere, If the melt contains more than 1.7 parts per million hydrogen, hydrogen gas will be rejected as bubbles during cooling or solidication, thereby causing porosity in the solidified metal.
  • the hydrogen content in the furnace atmosphere above the melt is such that the molten metal can absorb no more than the solid solubility limit of 1.7 parts per million. In this manner there will be no rejection of hydrogen during solidification and therefore no hydrogen bubble formation.
  • the ambient temperature in the furnace may range from about the melting point of -copper (l083 C.) to about 1300 C., and
  • FIG- URE 2 illustrates graphically the quantitative relationship between percent hydrogen in the atmosphere and the amount which can be dissolved in liquid copper at several temperatures.
  • the dissolved hydrogen in parts per million is plotted as the abscissa and the percent hydrogen in the atmosphere as the ordinate. From the graph, it can be seen that the percent hydrogen in the atmosphere should not exceed about l percent by volume at the melting temperature of 1083 C., or about 7 percent at 1200 C., in order to avoid formation of hydrogen bubbles.
  • the hydrogen content in the atmosphere above the melt should range from about 2 to 5 percent.
  • the combination of hydrogen and carbon monoxide in the atmosphere in controlled amounts offers the desired reduction in oxygen content and further avoids any adverse results where only one gas is used.
  • the carbon monoxide content will range from about 1 to l0 percent by volume, and a ratio of carbon dioxide to carbon monoxide is from about 2:1 to 1:20.
  • the carbon monoxide content is from about 4 to 8 percent 4by volume, and the ratio of carbon dioxide to carbon monoxide is from about 1:2 to 1:10.
  • carbon monoxide does not penetrate the melt and therefore reacts with the oxygen at or near the surface of the melt only.
  • hydrogen dissolves readily in the molten copper and will react with the oxygen deep in the bath.
  • carbon monoxide alone will attack the silicon carbide heating elements, and to avoid this a controlled amount of carbon dioxide is included in the atmosphere.
  • the ratio of carbon monoxide to carbon dioxide is particularly important. If the ratio is too low (i.e., the carbon dioxide content is high), the atmosphere will not be sutciently reducing to deoxidize the copper. If, on the other hand, the ratio is too high, the excessive reducing atmosphere will attack the silicon carbide heating elements.
  • copper rod was formed by passing a copper core rod having a diameter of 0.38 inch through a molten bath of copper contained in a crucible.
  • the molten copper was supplied to the crucible through an integrally connected spout extending from a refractory-lined melting furnace which was heated by a plurality of silicon carbide electric radiant heaters, as described above.
  • a reducing atmosphere was maintained over the molten copper in the furnace which comprised 5 percent hydrogen, 7 percent carbon monoxide, 0.7 percent carbon dioxide and the balance nitrogen, all percentages being by volume.
  • a protective atmosphere of nitrogen was maintained above the molten copper in the crucible.
  • the resulting cast rod exhibited high quality being substantially free from irregularities and contamination, and upon analysis showed an oxygen content of about 5 parts per million.
  • the reducing atmosphere maintained above the molten copper in the furnace comprised 13 percent hydrogen, 10 percent carbon monoxide, 1 percent carbon dioxide and the balance nitrogen, all percentages being by volume.
  • the resulting cast rod from this second run had a low oxygen content of 3 parts per million, but nevertheless was a poor quality exhibiting lhigh porosity resulting from hydrogen evolution.
  • a method of accreting copper onto a core rod comprising supplying to a crucible a melt of molten copper from a melting furnace, passing said core rod through the molten copper contained in said crucible to accrete copper thereon and removing the resulting cast rod from said crucible, the improvement comprising: maintaining above said melt in the melting furnace an atmosphere comprising from about 1 to 10 percent by volume hydrogen, about 1 to 10 percent by volume carbon monoxide, carbon dioxide, the ratio of carbon dioxide to carbon monoxide being from about 2:1 to 1:20, and the balance being an inert diluent, whereby the oxygen content in said melt is maintained at less than approximately 20 parts per million.
  • a method of accreting copper onto a core -rod comprising supplying to a crucible a melt of molten copper from a melting furnace, passing said core rod through the molten copper contained in said crucible to accrete copper thereon and removing the resulting larger cast rod from said crucible, the improvement comprising: maintaining above said melt in the melting furnace an atmosphere comprising from about 2 to 5 percent by volume hydrogen, about 4 to 8 percent by volume carbon monoxide, carbon dioxide, the ratio of carbon dioxide to carbon monoxide being from about 1:2 to 10:1, and the balance being nitrogen, whereby the oxygen content in said melt is maintained at less than approximately 20 parts per million.

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Description

n.1. mannen. Jn 3,484,280
mnosrnan cou'rnol. In DIP-Forums rnocnss rma prix 4. 196? 2 Sheets-$hoet 1 /IV VENTO? ROLAND R CARREKA'@ ATTRN'E Y 2 Sheets-Sheet 2 med April 4, 19?
1.o DussoLvEn HYoRoGEN' Ffm A TTR/VE Y United States Patent O 3,484,280 ATMOSPHERE CONTROL IN DIP-FORMING PROCESS Roland P. 'Carrekerg Jr., Schenectady, N.Y., assignor to General Electric Company, a corporation of New York Filed Apr. 4, 1967, Ser. No. 628,356 Int. Cl. C23c 1/10 U.S. Cl. 117--114 5 Claims ABSTRACT OF THE DISCLOSURE In the dip-forming process for accreting copper onto a core member passed upwardly through a crucible containing a molten bath of copper, a melt of molten copper is supplied to the crucible from a melting furnace. A reducing atmosphere comprising hydrogen, carbon monoxide, carbon dioxide, and an inert diluent in controlled amounts is maintained above the melt in the melting furnace, whereby the oxygen content in the melt is reduced to less than about parts per million.
The dip-forming process, such as used in casting metal, is now well known in the art. According to this process, an elongated body such as a metal rod is typically pretreated by passing it through a straightener, a surface cleaning apparatus, and then through a vacuum entrance chamber positioned below or at the bottom of a crucible containing a bath of molten material. A continuous elongated core or body is passed upwardly through the molten bath, which bath may have the same chemical composition as that of the core or a different composition. The molten material in the crucible accretes or deposits upon the outer surface of the core thereby increasing its crosssectional area appreciably. After emerging from the crucible, the resulting cast member is cooled as by a water spray from one or more jet nozzles at least sufficiently so that the cast member can be rolled or worked. From there, the cast member may be passed through a suitable roll mechanism where it is reduced in cross-sectional area and then passed to a suitable receiving means such as a take-up reel.
The quality of the copper rod cast by the dip-forming process is influenced to a large extent by the gases dissolved in the molten copper, which are dependent upon the composition of the atmosphere in contact with the molten metal. In casting copper, gas evolution results from the presence of excessive oxygen and/or hydrogen in the melt. The problem of gas contamination in the dipforming process has been previously recognized, and in one aspect formed the basis of U.S. Patent No. 3,060,053 to Carreker and Parke and assigned to the assignee of this invention.
Under the conditions employed in the dip-forming process, oxygen and hydrogen present in the atmosphere above the molten-metal can be dissolved by and/ or react with the motlen material. Oxygen may cause the formation of undesirable oxides. It is recognized that copper having an oxygen content greater than approximately 20 parts per million results in progressive deterioration in casting quality. Also, the presence of hydrogen alone, or hydrogen and oxygen concurrently, in molten metal in sufficient amounts will cause formation of gas bubbles upon solidifcation of the accreted material on the cast member. The formation of oxides, gas bubbles and/ or voids not only adversely affects the quality of the product, but also deleteriously affects the uniform accretion of molten material onto the core by creating regions of relatively poor thermal conductivity within a mass of relatively good thermal conductivity. Thus, the effect of oxygen and hydrogen is not confined to the oxide phases and bubbles they create,
rice
but is magnified due to the irregularities in heat transfer they produce, causing substantial non-uniformity in the external contour of the accreted coating. Bubbles, voids, oxide phases, internal discontinuities, and irregular accretion are all undesirable in that they promote or cause the formation of cracks and fissures when stresses are imposed, as by bending, rolling, drawing or the like. A product manifesting such defects is generally not acceptable.
According to U.S. Patent 3,060,053, referred to above, the oxygen content in the molten metal is reduced to a very low amount by utilizing graphite or comparable reducing means which will unite with the oxygen in the molten metal to form a gaseous product which escapes from the molten copper. In addition, an inert atmosphere such as nitrogen is maintained above the surface of the melt to protect the melt from the air. Such a furnace system will produce satisfactorily low oxygen content copper for use with dip-forming, if the furnace system is free of substantial air leaks and is allowed to come to substantial equilibrium. However, air leaks may be expected in a large industrial furnace, particularly under charging conditions, and long residence times for equilibration are not realized. Experience has demonstrated that graphite furnace linings and graphite heating elements are rapidly consumed by oxygen from undesired air leaks. Ceramic furnace 1inings and silicon carbide electrical resistance heating elements are not harmed by such air leaks. However, oxygen from the air may react with the molten copper to form copper oxide slag, which will attack or erode the silicon carbide furnace parts. Use of a reducing atmosphere, rather than a neutral or inert atmosphere such as nitrogen, is desirable. Hydrogen is a reducing gas, but, as explained above, this gas is readily absorbed by the molten copper with can result in the formation. of gas bubbles, thereby causing porosity and interfering with uniform heat transfer. Carbon monoxide is another reducing gas, but it is insoluble in molten copper and can react with the melt only at its surface. Therefore, carbon monoxide is relatively slow in reducing the oxygen content in a relatively deep melt. Further, strongly reducing atmospheres harmfully affect silicon carbide heating elements in that such atmospheres cause the formation of volatile silicon monoxide, which results in the eventual distintegration of the heating element.
The purpose of this invention is to provide a controlled reducing atmosphere above the molten copper which is sufficiently reducing to maintain the oxygen in the molten copper at less than approximately 20 parts per million, yet sufficiently oxidizing to avoid substantial erosion or attack of silicon carbide furnace elements employed in the system, and sufiiciently low in hydrogen to avoid evolution of hydrogen bubbles during solidification in the dip-forming process.
According to the present invention, molten copper from a melting furnace is supplied to a crucible through which a continuous, elongated core rod is passed, whereby molten metal deposits or accretes to the rod. A reducing atmosphere comprising 1 to 10 percent by volume hydrogen, 1 to 10 percent carbon monoxide, carbon dioxide, the ratio of carbon dioxide to carbon monoxide being from about 2:1 to 1:20, and the balance being an inert diluent such as nitrogen is maintained above the molten metal. By reason of the reducing atmosphere maintained 3 tion between the atmosphere and the melt at low oxygen contents is reduced.
Reference is now had to the following detailed specification and to the accompanying drawings illustrating a preferred embodiment of the invention.
FIGURE 1 is a perspective view partially in section of an apparatus for practicing the present invention.
FIGURE 2 is a graph showing the solubility of hydrogen in copper.
Referring to FIGURE 1, core rod is supplied to a drawing apparatus 12 located adjacent a suitable shaving apparatus 14 which shaves a thin layer of metal from the periphery of the rod to remove the oxide coating and other surface contaminants therefrom. If desired, other cleaning means such as chemical cleaning means, may be utilized for removing the oxide coating and cleaning the surface of the rod. The rod is passed through a suitable drive means, including capstan 15 and drive rolls 16 contained in housing 18, and from there into tube 20. Members 12, 14, 18 and 20 are sealed and interconnected to a suitable passageway, and tube 20 has connected thereto exhaust tube 22 and evacuating pump 24 to maintain a vacuum in the passageway. Entry port member or nozzle 26 is mounted in the upper end of tube 20 and extends into crucible 28 which is maintained at the desired elevated temperature by suitable heating means such as electric induction heater 30. Core lrod 10 is fed through nozzle 2-6 and into crucible 28 Where the rod comes into contact with the molten copper which accretes to the rod, as described hereinafter in greater detail.
Molten copper is supplied to crucible 28 from melting ifurnace indicated generally by the numeral 32, which is heated by a plurality of silicon carbide electric radiant heaters 34. Cathode copper plates 35, or other suitable feed material of low oxygen content, is supplied to the furnace 32 by any suitable means such as a mechanical drive means (not shown). Desirably the furnace is provided with a sloping or inclined section 36 and an integral horizontal section 38. The cathode copper plates are charged to section 36 of the furnace through a dapper-type door (not shown) and melted gradually on the incline as they pass to the horizontal section 38 where a pool of molten metal collects. The molten metal flows by displacement over a Weir 40 into a level control section 42 of the furnace. A suitable liquid level sensing control, indicated generally by the reference numeral 44, which is com- -monly employed in the art, controls subsurface flow through passageway 45 into dip-forming crucible 28. An electric probe 46 in the crucible senses the bath level and automatically regulates the level sensing control to maintain a constant level in the crucible.
Copper supplied to the furnace may contain an undesirably high oxygen content, or air may leak to the furnace such as through the entranceway to the furnace through which the copper is charged. For this reason, it is necessary to maintain a controlled reducing atmosphere above the molten metal. The reducing atmosphere is supplied to the furnace through line 48 from a suitable source (not shown). The reducingr atmosphere lowers the oxygen content of the copper to less than 20 parts per million and maintains this low level. As a result, the molten copper fed to the dip-forming crucible has this low oxygen content, and further does not contain sufficient hydrogen to cause hydrogen bubble formation during soliditication. Desirably, an atmosphere of an inert gas such as nitrogen is maintained above the molten metal in the crucible which may be supplied to the crucible through line 49 from source 50. As the core rod 10 passes through the molten bath of metal in the crucible, copper accretes progressively thereon thereby forming a rod of increased diameter with molten metal substantially bonded to the core rod.
An elongated tube 52 extends upwardly from crucible 28, and the resulting cast rod having copper accreted thereto is passed out of the crucible to the extension tube.
The cast rod emerging from the crucible and extension tube is at a relatively high temperature and is cooled somewhat by cooling means 54, such as a water spray nozzle, before the rod is passed through direction changing rolls 56. From there the cast rod is directed to a suitable rolling mill and coiling apparatus (not shown) and to a storage area as desired.
lIn practicing this invention, the reducing atmosphere supplied to the furnace comprises about 1 to 10 percent by volume hydrogen, 1 to 10 percent by volume carbon monoxide, carbon dioxide, the ratio of carbon dioxide to carbon monoxide being from about 2:1 to 1:20, and the balance being nitrogen or another suitable inert diluent. As mentioned above, the reducing gases of the atmosphere, that is, the hydrogen and carbon monoxide, react with the oxygen present in the molten metal thereby reducing the oxygen content to less than 2() parts per million. The oxidizing tendency of the atmosphere at a given temperature is specified by the ratio of carbon dioxide to carbon monoxide or by the ratio of water vapor to hydrogen; specifying either one of these ratios specifies the other, at equilibrium, according to the chemical Equation 1 Coz-l-HzCO +H2O 1 The oxygen content of the molten copper, at equilibrium is governed by Equation 2.
1/zOZO (in copper) (2) which is related, through Equation 2, to the CO2/CO ratio by Equations 3 and 4 and 5.
O (in copper) =K2[O2]1/2 (4) per million is related to the ratio of CO2 to CO in the atmosphere by Equation 6.
[CO2]N [CO2] O KZKS [G01 N14 [C01 6) The constant K2K3 is approximately 7, 14 and 16 at 1100", 1200, and 1300 C., respectively. Thus, as a useful first approximation, the oxygen content of the molten copper in parts per million may be said to be about ten times the ratio of per cent carbon dioxide to percent carbon monoxide in the atmosphere, at equilibrium.
The presence of hydrogen offers more complete assurance against oxidation. Hydrogen is soluble in molten copper, and the amount dissolved is related to the hydrogen content in the atmosphere above the molten metal and to the temperature. Solid copper at its melting point of 1083o C. can retain up to 1.7 parts per million of hydrgen in solid solution in equilibrium with a hydrogen pressure of 1.0 atmosphere, If the melt contains more than 1.7 parts per million hydrogen, hydrogen gas will be rejected as bubbles during cooling or solidication, thereby causing porosity in the solidified metal. In order to avoid the formation of hydrogen bubbles, the hydrogen content in the furnace atmosphere above the melt is such that the molten metal can absorb no more than the solid solubility limit of 1.7 parts per million. In this manner there will be no rejection of hydrogen during solidification and therefore no hydrogen bubble formation. In typical dip-forming operations, the ambient temperature in the furnace may range from about the melting point of -copper (l083 C.) to about 1300 C., and
more preferably from about 1125 C. to 1175 C. FIG- URE 2 illustrates graphically the quantitative relationship between percent hydrogen in the atmosphere and the amount which can be dissolved in liquid copper at several temperatures. In the graph, the dissolved hydrogen in parts per million is plotted as the abscissa and the percent hydrogen in the atmosphere as the ordinate. From the graph, it can be seen that the percent hydrogen in the atmosphere should not exceed about l percent by volume at the melting temperature of 1083 C., or about 7 percent at 1200 C., in order to avoid formation of hydrogen bubbles. In the preferred operating conditions, the hydrogen content in the atmosphere above the melt should range from about 2 to 5 percent.
It will be observed that the combination of hydrogen and carbon monoxide in the atmosphere in controlled amounts offers the desired reduction in oxygen content and further avoids any adverse results where only one gas is used. Generally, the carbon monoxide content will range from about 1 to l0 percent by volume, and a ratio of carbon dioxide to carbon monoxide is from about 2:1 to 1:20. In the preferred embodiment the carbon monoxide content is from about 4 to 8 percent 4by volume, and the ratio of carbon dioxide to carbon monoxide is from about 1:2 to 1:10. However, carbon monoxide does not penetrate the melt and therefore reacts with the oxygen at or near the surface of the melt only. On the other hand, hydrogen dissolves readily in the molten copper and will react with the oxygen deep in the bath. Also, carbon monoxide alone will attack the silicon carbide heating elements, and to avoid this a controlled amount of carbon dioxide is included in the atmosphere. For these reasons, the ratio of carbon monoxide to carbon dioxide is particularly important. If the ratio is too low (i.e., the carbon dioxide content is high), the atmosphere will not be sutciently reducing to deoxidize the copper. If, on the other hand, the ratio is too high, the excessive reducing atmosphere will attack the silicon carbide heating elements.
To further illustrate the invention, copper rod was formed by passing a copper core rod having a diameter of 0.38 inch through a molten bath of copper contained in a crucible. The molten copper was supplied to the crucible through an integrally connected spout extending from a refractory-lined melting furnace which was heated by a plurality of silicon carbide electric radiant heaters, as described above. A reducing atmosphere was maintained over the molten copper in the furnace which comprised 5 percent hydrogen, 7 percent carbon monoxide, 0.7 percent carbon dioxide and the balance nitrogen, all percentages being by volume. Also, a protective atmosphere of nitrogen was maintained above the molten copper in the crucible. The resulting cast rod exhibited high quality being substantially free from irregularities and contamination, and upon analysis showed an oxygen content of about 5 parts per million. In a second run, the reducing atmosphere maintained above the molten copper in the furnace comprised 13 percent hydrogen, 10 percent carbon monoxide, 1 percent carbon dioxide and the balance nitrogen, all percentages being by volume. The resulting cast rod from this second run had a low oxygen content of 3 parts per million, but nevertheless was a poor quality exhibiting lhigh porosity resulting from hydrogen evolution.
I claim:
1. In a method of accreting copper onto a core rod comprising supplying to a crucible a melt of molten copper from a melting furnace, passing said core rod through the molten copper contained in said crucible to accrete copper thereon and removing the resulting cast rod from said crucible, the improvement comprising: maintaining above said melt in the melting furnace an atmosphere comprising from about 1 to 10 percent by volume hydrogen, about 1 to 10 percent by volume carbon monoxide, carbon dioxide, the ratio of carbon dioxide to carbon monoxide being from about 2:1 to 1:20, and the balance being an inert diluent, whereby the oxygen content in said melt is maintained at less than approximately 20 parts per million.
2. A method according to claim 1 wherein the hydrogen content is from about 2 to 5 percent.
3. A method according to claim 1 wherein the carbon monoxide content is from about 4 to 81 percent.
4. A method according to claim 1 wherein the ratio of carbon dioxide to carbon monoxide is from about 1:2 to 1:10.
5. In a method of accreting copper onto a core -rod comprising supplying to a crucible a melt of molten copper from a melting furnace, passing said core rod through the molten copper contained in said crucible to accrete copper thereon and removing the resulting larger cast rod from said crucible, the improvement comprising: maintaining above said melt in the melting furnace an atmosphere comprising from about 2 to 5 percent by volume hydrogen, about 4 to 8 percent by volume carbon monoxide, carbon dioxide, the ratio of carbon dioxide to carbon monoxide being from about 1:2 to 10:1, and the balance being nitrogen, whereby the oxygen content in said melt is maintained at less than approximately 20 parts per million.
References Cited UNITED STATES PATENTS 1,903,497 4/ 1933 Alexander et al. 75-76 1,958,754 5/1934 Holley 75--76 X 2,060,073 11/ 1936 Heuer 75-76 X 2,060,133 11/1936 Summey 75--76 X 2,060,137 11/1936 Bahney 75-76 2,166,354 7/1939 Heuer 75-76 2,190,570 2/ 1940 Orlando 75-76 2,216,519 10/1940 Quarnstrom 117--114 X 3,235,960 2/1966 Carreker 117-128 X FOREIGN PATENTS 499,728 2/ 1954 Canada.
ALFRED L. LEAVITT, Primary Examiner I. R. BATTEN, JR., Assistant Examiner' U.S. Cl. X.R.
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US3685570A (en) * 1968-11-14 1972-08-22 Bengt Fredrikson Means for casting
US3987224A (en) * 1975-06-02 1976-10-19 General Electric Company Oxygen control in continuous metal casting system
US3995679A (en) * 1974-12-20 1976-12-07 General Electric Company Continuous casting apparatus, and a method of casting
DE2733075A1 (en) * 1976-07-20 1978-04-13 Battelle Memorial Institute PROCESS FOR COATING A WIRE-SHAPED OBJECT WITH A THERMAL FUSIBLE MATERIAL
WO1994029048A1 (en) * 1993-06-08 1994-12-22 Mannesmann Ag Process and device for making semi-finished products
US5451429A (en) * 1993-08-27 1995-09-19 The Boc Group Plc Method and apparatus for treating freshly metallized substrates
CN102615271A (en) * 2011-08-29 2012-08-01 杭州富通昭和铜业有限公司 Method for producing bright oxygen-free copper rod
EP2829625A4 (en) * 2012-03-23 2015-12-23 Aleksandr Aleksandrovich Kulakovsky Device for applying a coating to an extended article
CN114657492A (en) * 2022-03-09 2022-06-24 杭州富通集团有限公司 Method for preparing oxygen-free copper rod by dip coating and oxygen-free copper rod prepared by method
US11753700B2 (en) 2017-05-10 2023-09-12 Haldor Topsøe A/S Process for reducing the content of oxygen in metallic copper

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US3887721A (en) * 1972-12-20 1975-06-03 Armco Steel Corp Metallic coating method
CN113182499A (en) * 2021-05-03 2021-07-30 芜湖恒泰有色线材股份有限公司 Technology for adding nitrogen into carbon monoxide for quick deoxidization in copper smelting by upward drawing method

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US1903497A (en) * 1931-02-05 1933-04-11 Harry H Alexander Metallurgy of copper
US1958754A (en) * 1932-02-23 1934-05-15 Carlos E Holley Treatment of copper and other metals
US2060073A (en) * 1930-06-05 1936-11-10 American Metal Co Ltd Copper refining method
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US2166354A (en) * 1936-11-07 1939-07-18 American Metal Co Ltd Copper refining process
US2190570A (en) * 1937-03-25 1940-02-13 Metallurg Bresciana Gia Tempin Process for treating copper
US2216519A (en) * 1938-01-03 1940-10-01 Bundy Tubing Co Making tubing
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US3235960A (en) * 1961-03-24 1966-02-22 Gen Electric Process for the continuous formation of intermediates

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CA499728A (en) * 1954-02-02 Wolf Rudolf Process for the deoxidation of copper
US2060073A (en) * 1930-06-05 1936-11-10 American Metal Co Ltd Copper refining method
US1903497A (en) * 1931-02-05 1933-04-11 Harry H Alexander Metallurgy of copper
US2060133A (en) * 1931-05-08 1936-11-10 Scovill Manufacturing Co Process for treating metals
US1958754A (en) * 1932-02-23 1934-05-15 Carlos E Holley Treatment of copper and other metals
US2060137A (en) * 1934-10-26 1936-11-10 Scovill Manufacturing Co Process of refining metals
US2166354A (en) * 1936-11-07 1939-07-18 American Metal Co Ltd Copper refining process
US2190570A (en) * 1937-03-25 1940-02-13 Metallurg Bresciana Gia Tempin Process for treating copper
US2216519A (en) * 1938-01-03 1940-10-01 Bundy Tubing Co Making tubing
US3235960A (en) * 1961-03-24 1966-02-22 Gen Electric Process for the continuous formation of intermediates

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3685570A (en) * 1968-11-14 1972-08-22 Bengt Fredrikson Means for casting
US3995679A (en) * 1974-12-20 1976-12-07 General Electric Company Continuous casting apparatus, and a method of casting
US3987224A (en) * 1975-06-02 1976-10-19 General Electric Company Oxygen control in continuous metal casting system
DE2733075A1 (en) * 1976-07-20 1978-04-13 Battelle Memorial Institute PROCESS FOR COATING A WIRE-SHAPED OBJECT WITH A THERMAL FUSIBLE MATERIAL
US5722151A (en) * 1993-06-08 1998-03-03 Mannesmann Aktiengesellschaft Process for making semi-finished products
WO1994029048A1 (en) * 1993-06-08 1994-12-22 Mannesmann Ag Process and device for making semi-finished products
CN1043317C (en) * 1993-06-08 1999-05-12 曼内斯曼股份公司 Process and device for making semi-finished products
US5451429A (en) * 1993-08-27 1995-09-19 The Boc Group Plc Method and apparatus for treating freshly metallized substrates
CN102615271A (en) * 2011-08-29 2012-08-01 杭州富通昭和铜业有限公司 Method for producing bright oxygen-free copper rod
CN102615271B (en) * 2011-08-29 2014-04-16 杭州富通昭和铜业有限公司 Method for producing bright oxygen-free copper rod
EP2829625A4 (en) * 2012-03-23 2015-12-23 Aleksandr Aleksandrovich Kulakovsky Device for applying a coating to an extended article
US11753700B2 (en) 2017-05-10 2023-09-12 Haldor Topsøe A/S Process for reducing the content of oxygen in metallic copper
CN114657492A (en) * 2022-03-09 2022-06-24 杭州富通集团有限公司 Method for preparing oxygen-free copper rod by dip coating and oxygen-free copper rod prepared by method

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DE1758099A1 (en) 1972-03-30
CH493646A (en) 1970-07-15
FR1565019A (en) 1969-04-25
ES352371A1 (en) 1969-08-01
SE326257B (en) 1970-07-20
GB1197352A (en) 1970-07-01
AT286742B (en) 1970-12-28

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