US3728144A - Method for coating metal substrates with molten metal - Google Patents
Method for coating metal substrates with molten metal Download PDFInfo
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- US3728144A US3728144A US00134738A US3728144DA US3728144A US 3728144 A US3728144 A US 3728144A US 00134738 A US00134738 A US 00134738A US 3728144D A US3728144D A US 3728144DA US 3728144 A US3728144 A US 3728144A
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- 229910052751 metal Inorganic materials 0.000 title abstract description 76
- 239000002184 metal Substances 0.000 title abstract description 76
- 239000011248 coating agent Substances 0.000 title abstract description 33
- 238000000576 coating method Methods 0.000 title abstract description 33
- 239000000758 substrate Substances 0.000 title abstract description 33
- 238000000034 method Methods 0.000 title abstract description 24
- 238000010438 heat treatment Methods 0.000 abstract description 17
- 238000007654 immersion Methods 0.000 abstract description 17
- 238000001816 cooling Methods 0.000 abstract description 16
- 230000008569 process Effects 0.000 description 16
- 239000007789 gas Substances 0.000 description 9
- 150000002739 metals Chemical class 0.000 description 8
- 229910052782 aluminium Inorganic materials 0.000 description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 7
- 239000011247 coating layer Substances 0.000 description 7
- 230000008018 melting Effects 0.000 description 7
- 238000002844 melting Methods 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 6
- 238000005554 pickling Methods 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- 238000000137 annealing Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- 230000008020 evaporation Effects 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000004907 flux Effects 0.000 description 3
- 239000004519 grease Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000012266 salt solution Substances 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- 229910000677 High-carbon steel Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910001566 austenite Inorganic materials 0.000 description 1
- 229910052728 basic metal Inorganic materials 0.000 description 1
- 150000003818 basic metals Chemical class 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000021110 pickles Nutrition 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/003—Apparatus
- C23C2/0034—Details related to elements immersed in bath
- C23C2/00342—Moving elements, e.g. pumps or mixers
- C23C2/00344—Means for moving substrates, e.g. immersed rollers or immersed bearings
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/003—Apparatus
- C23C2/0035—Means for continuously moving substrate through, into or out of the bath
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/003—Apparatus
- C23C2/0038—Apparatus characterised by the pre-treatment chambers located immediately upstream of the bath or occurring locally before the dipping process
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
- C23C2/022—Pretreatment of the material to be coated, e.g. for coating on selected surface areas by heating
- C23C2/0224—Two or more thermal pretreatments
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
- C23C2/024—Pretreatment of the material to be coated, e.g. for coating on selected surface areas by cleaning or etching
Definitions
- the present invention relates to a method and apparatus for coating metal substrates with molten metal and to the coated metal substrates so produced. More particularly, the present invention relates to a method and apparatus for coating steel wires with metals, such as copper, tin, lead or aluminum; and to the coated steel wire so produced.
- a metal substrate is subjected to a relatively large number of separate treatments.
- steel wire is first annealed in order to obtain the desired degree of toughness and tensile strength.
- the annealed steel wire is ordinarily pickled and rinsed, processed with a salt solution or flux, dried, dipped into the proper metallizing bath and then cooled down.
- the purpose of the pickling step is to remove grease, dirt and the like, as well as oxides which may be formed during the heat treatment.
- the lluxing step is employed to provide the wire with good moistening characteristics for the liquid coating to be subsequently applied.
- a conventional process for metal coating or metallizing of the type described above suifers from a number of disadvantages. For example, oxidation which occurs during the heat treatment is disadvantageous because it requires the additional pickling step. Further, the pickling and fluxing steps are disadvantageous because the metal substrate thereafter needs to be dried.
- a further disadvantage results from the fact that after the annealing process the substrate is subsequently cooled down to the temperature of the rinsing and washing water during the pickling, rinsing and fluxing treatments.
- the metal substrate is thereafter passed through the metallizing bath it absorbs a substantial amount of the heat present in the metallizing bath. Consequently, it is necessary to supply the metallizing bath continuously with a large quantity of heat in order to balance the removal of heat absorbed by the substrate and to maintain the temperature of the metallizing bath at a constant level.
- a further disadvantage of the conventional type of process results from the fact that pickling with hydrochloric or sulfuric acid entails substantial ditficulties with respect to providing the necessary apparatus for the removal of harmful vapors and used acid.
- treatment of the metal wire with salt solutions or flux is also disadvantageous because it causes sludge deposits to form in the metallizing bath.
- the present invention relates to a method and apparatus for continuous coating of a metal substrate with a molten metal wherein the metal substrate is coated with molten metal in an immersion zone maintained under vacuum. More particularly, the metal substrate under vacuum is successively annealed at an elevated temperature in a heating zone, cooled in a cooling zone and coated with the molten metal in the immersion zone.
- FIG. 1 is a schematic illustration of an apparatus for continuous heat treatment and metallizing in accordance with one embodiment of the present invention.
- FIG. 2 is a schematic illustration of an apparatus for continuous heat treatment and metallizing in accordance with a second embodiment of the present invention.
- FIG. 1 DESCRIPTION OF THE PREFERRED EMBODIMENTS Apparatus for continuous heat treatment and subsequent metallizing of a metal substrate, namely, wire 1 is illustrated in FIG. 1.
- the metal substrate which may be utilized in the present invention includes any wire, strip, plate or similar extended form of metal product which it is desired to coat with a molten metal or to metallize.
- the metal wire 1 is fed from supply spool 2 and via guide rollers 3, 4 and 5 to a capstan 6.
- Guide roller 4 is mounted in an immersion bath 7 containing a molten coating metal.
- the basic metal treating operations are carried out in a vacuum chamber 8.
- the supply spool 2 and/or capstan 6 may be mounted inside or outside the vacuum chamber 8.
- the required vacuum in vacuum chamber 8 may be obtained and maintained by any conventional means, as, for example, by means of the process described in US. Pat. No. 2,384,500.
- the vacuum may be obtained by connecting conventional pumps or other conventional equipment for producing a high vacuum, to vacuum chamber 8 by means of conduit 9.
- a heater 10 is provided in chamber 8 to heat wire 1.
- the heater 10 may be of any conventional design whereby Wire 1 may be heated, for example, by radiation, electron bombardment, direct resistance heating or the like.
- Chamber 8 is also provided with cooling means 11 for cooling the heated or annealed wire 1.
- Cooling apparatus 11 may be composed of water-cooled rollers or any other conventional suitable cooling apparatus.
- the apparatus of the present invention may also include a means H for introducing a reducing gas such as hydrogen into the area of immersion bath 7 where the wire 1 enters and leaves the immersion bath 7.
- FIG. 2 A second embodiment of the present invention is illustrated in FIG. 2.
- supply spool 2 and guide roller 5 are mounted outside of the vacuum chamber 8.
- the apparatus includes a plurality of smaller conduits or ports 9 which assist in maintaining a vacuum in chamber 8 in the area where wire 1 is fed from supply spool 2 to the interior of vacuum chamber 8.
- the means H for supplying a reducing gas to the process includes a first means for supplying reducing gas to the interior of chamber 8 at the point where wire 1 enters immersion bath 7 and a second means for supplying reducing gas to a second point outside vacuum chamber 8 at the point where the wire 1 exits from the immersion bath 7.
- the wire 1 is fed from supply spool 2 through vacuum chamber 8.
- the vacuum in vacuum chamber 8 will be maintained in the range of about 10- to l() torr (l torr being equivalent to a pressure of 1 mm. of mercury).
- the wire 1 after being fed from supply spool 2 is heated by heater 10 to a temperature generally above about 700 C. to thereby anneal wire 1.
- a metallically clean surface is obtained free from oxides, grease, oil and the like; and possible gases dissolved in the metal are removed.
- the wire 1 consists of steel with a high carbon content, the wire 1 will normally be heated to a temperature in the range of about 800 to 1000 C., e.g. 900 C., in order to obtain an austenite steel structure.
- the heat treatment by means of heater 10 in vacuum chamber 8 produces a clean, metallic, thermically etched wire surface which may be coated with molten metal without the necessity of using the fiuxing treatment normally used in prior art processes.
- the temperature of the wire 1 when it enters the metallizing bath is of great importance. If this temperature is too high, the danger exists that a reaction layer may be formed between the metal base of the wire 1 and the coating metal which is undesirably thick. In this case the coated wire 1 is likely to be brittle and when the coated wire is bent or folded small cracks may develop in the coating layer. Thus, a high degree of intermetallic combination or brittleness occurs when the temperature is too high so as to produce intermetallic diifusion.
- the temperature of the wire 1 is not too low when entering the immersion bath 7. Thus, if the temperature is too low the adhesion between the wire 1 and the coating metal will be inadequate.
- the heated annealed wire 1 is subsequently passed through cooler 11 which cools the temperature of wire 1 to the proper level.
- the particular temperature to which wire 1 is cooled in cooler 11 depends upon the nature of the substrate as well as the nature of the coating metal which is subsequently employed. The optimum temperature for any given combination of substrate and coating metal can be readily determined and should be selected to provide an operation in which the formation of a brittle reaction layer is minimized while at the same time producing an adequate adhesion between the wire 1 and the coating metal employed.
- the wire 1 is made of a high carbon steel it is essential for proper annealing and isothermal hardening of the wire 1 to rapidly cool it down to a temperature in the range of about 400 to 600 C., e.g. 500 C. Thereafter, a controlled cooling of the wire 1 at a lower rate of cooling may be employed if desired, with respect to the particular type of coating metal which may subsequently be employed.
- the coating metals which can be most advantageously employed in the present invention, are metals with a low vapor pressure in the proximity of their melting temperature, such as, for example, aluminum, copper, tin and indium or alloys of these metals.
- the temperature of the coating metal in the bath 7 is preferably 'kept at a temperature level that is approximately 1 to 50 C. higher than the melting temperature. In this way only a small amount of metal will be lost through evaporation with the result that the amount of metal deposition on the walls of vacuum chamber 8 is minimized and further the best coating layers with the lowest percentages of intermetallic combinations are obtained.
- the following table lists the melting temperatures, the vapor pressure and evaporation speeds of a number of metals with low vapor pressures which may be utilized in the present invention:
- the coating layers obtained by the process of the present invention are of a high quality with respect to adhesion of the metal coating and resistance to chipping, as well as uniformity of coating thickness.
- a mild steel wire i.e., a wire with a low carbon content; namely 0.10% was passed through a bath filled with molten aluminum.
- the temperature of the molten aluminum was about 670 C. and the vacuum maintained above the bath was about 5 10- torr.
- the mild steel wire was first annealed at a temperature of about 850 C. and subsequently cooled down to a temperature of about 500 C. just before it was passed into the molten aluminum bath.
- the bath contained 0.0% silicon; in a second test, the bath contained 2.0% silicon; and in a third test, the bath contained 4.0% silicon. All of the wires coated in the above experiments were found to have a qualitatively good coating layer.
- the present invention carried out as described above was found to have the following advantages over the processes of the prior art. First, it was found that in carrying out the heat treatment under vacuum no oxidation occurred; and further, that any grease and the like evaporated at the elevated temperature and reduced pressure employed. Further it was found that the metal substrate after annealing remains in a thermically etched state and is in excellent condition for thorough moistening in the molten metal bath. Also, it was found that it was not necessary to pickle, rinse, flux and dry the wire after annealing and before metal coating. In addition, since it was found possible to eliminate the pickling step there is no longer any danger or special equipment involved in the removal of harmful gases. Further, since no fluxing process was required, no sludge deposits were produced in the metallizing bath.
- a process for continuous coating of a metal substrate with a molten metal comprising annealing a substrate at an elevated temperature in a heating zone maintained under vacuum, cooling the annealed substrate in a cooling zone maintained under vacuum and coating the cooled annealed metal substrate 6 with a molten metal in an immersion zone maintained under vacuum.
- said substrate is a carbon steel wire which is annealed at a temperature in the range of about 700 to 1000 C. in said heating zone and cooled to a temperature in the range of about 400 to 600 C. in said cooling zone.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Coating With Molten Metal (AREA)
- Heat Treatment Of Strip Materials And Filament Materials (AREA)
Abstract
A METHOD AND APPARATUS FOR CONTINUOUS COATING OF A METAL SUBSTRATE WITH A MOLTEN METAL IN WHICH A METAL SUBSTRATE IS SUCCESSIVELY ANNEALED AT AN ELEVATED TEMPERATURE IN A HEATING ZONE, COOLED IN A COOLING ZONE AND COATED WITH A MOLTEN METAL IN AN IMMERSION ZONE, WHEREIN THE HEATING ZONE, THE COOLING ZONE AND THE IMMERSION ZONE ARE MAINTAINED UNDER A VACUUM.
Description
A ril 17, 1973 VAN POUCKE 3,728,1 4
METHOD FOR COATING METAL SUBSTRATES WITH MOLTEN METAL Filed April 16, 1971 INVENTOR LIONEL VAN POUCKE fllflwflmy ATTORIEYS United States Patent O 3,728,144 METHOD FOR COATING METAL SUBSTRATES WITH MOLTEN METAL Lionel Van Poucke, Kortrijk, Belgium, assiguor to N.V. Bekaert S.A., Zwevegem, Belgium Filed Apr. 16, 1971, Ser. No. 134,738 Claims priority, application Netherlands, Apr. 24, 1970, 7006051 Int. Cl. C23c 1/00 US. Cl. 117-51 7 Claims ABSTRACT OF THE DISCLOSURE A method and apparatus for continuous coating of a metal substrate with a molten metal in which a metal substrate is successively annealed at an elevated temperature in a heating zone, cooled in a cooling zone and coated with a molten metal in an immersion zone, wherein the heating zone, the cooling zone 'and the immersion zone are maintained under a vacuum.
BACKGROUND OF THE INVENTION Field of the invention The present invention relates to a method and apparatus for coating metal substrates with molten metal and to the coated metal substrates so produced. More particularly, the present invention relates to a method and apparatus for coating steel wires with metals, such as copper, tin, lead or aluminum; and to the coated steel wire so produced.
Description of the prior art In conventional processes of metal coating or metallizing, a metal substrate is subjected to a relatively large number of separate treatments. In a typical process, for example, steel wire is first annealed in order to obtain the desired degree of toughness and tensile strength. 'Ihereafter, the annealed steel wire is ordinarily pickled and rinsed, processed with a salt solution or flux, dried, dipped into the proper metallizing bath and then cooled down. The purpose of the pickling step is to remove grease, dirt and the like, as well as oxides which may be formed during the heat treatment. The lluxing step is employed to provide the wire with good moistening characteristics for the liquid coating to be subsequently applied.
A conventional process for metal coating or metallizing of the type described above suifers from a number of disadvantages. For example, oxidation which occurs during the heat treatment is disadvantageous because it requires the additional pickling step. Further, the pickling and fluxing steps are disadvantageous because the metal substrate thereafter needs to be dried.
A further disadvantage results from the fact that after the annealing process the substrate is subsequently cooled down to the temperature of the rinsing and washing water during the pickling, rinsing and fluxing treatments. Thus, when the metal substrate is thereafter passed through the metallizing bath it absorbs a substantial amount of the heat present in the metallizing bath. Consequently, it is necessary to supply the metallizing bath continuously with a large quantity of heat in order to balance the removal of heat absorbed by the substrate and to maintain the temperature of the metallizing bath at a constant level.
A further disadvantage of the conventional type of process results from the fact that pickling with hydrochloric or sulfuric acid entails substantial ditficulties with respect to providing the necessary apparatus for the removal of harmful vapors and used acid. In addition, treatment of the metal wire with salt solutions or flux is also disadvantageous because it causes sludge deposits to form in the metallizing bath.
3,7 28,144 Patented Apr. 17, 1973 'ice From the foregoing discussion it. will be clear that conventional metal coating or metallizing operations pose a considerable number of serious problems because of the relatively large number of separate treatments that are involved. The apparatus employed needs to be quite complicated which inherently results in high investment costs.
SUMMARY OF THE INVENTION The present invention relates to a method and apparatus for continuous coating of a metal substrate with a molten metal wherein the metal substrate is coated with molten metal in an immersion zone maintained under vacuum. More particularly, the metal substrate under vacuum is successively annealed at an elevated temperature in a heating zone, cooled in a cooling zone and coated with the molten metal in the immersion zone.
It is an object of the present invention to provide an improved process for coating metal substrates with molten metal which is simpler and less expensive than prior art processes.
It is a further object of the present invention to provide improved apparatus for coating metal substrates with molten metal which is simpler and less expensive than apparatus of the prior art.
It is a still further object of the present invention to provide improved metal-coated metal substrate products.
Other objects and advantages of the present invention will become apparent from the following description taken in conjunction with the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a schematic illustration of an apparatus for continuous heat treatment and metallizing in accordance with one embodiment of the present invention; and
FIG. 2 is a schematic illustration of an apparatus for continuous heat treatment and metallizing in accordance with a second embodiment of the present invention.
DESCRIPTION OF THE PREFERRED EMBODIMENTS Apparatus for continuous heat treatment and subsequent metallizing of a metal substrate, namely, wire 1 is illustrated in FIG. 1. The metal substrate which may be utilized in the present invention includes any wire, strip, plate or similar extended form of metal product which it is desired to coat with a molten metal or to metallize. The metal wire 1 is fed from supply spool 2 and via guide rollers 3, 4 and 5 to a capstan 6. Guide roller 4 is mounted in an immersion bath 7 containing a molten coating metal.
The basic metal treating operations are carried out in a vacuum chamber 8. The supply spool 2 and/or capstan 6 may be mounted inside or outside the vacuum chamber 8. The required vacuum in vacuum chamber 8 may be obtained and maintained by any conventional means, as, for example, by means of the process described in US. Pat. No. 2,384,500. The vacuum may be obtained by connecting conventional pumps or other conventional equipment for producing a high vacuum, to vacuum chamber 8 by means of conduit 9.
A heater 10 is provided in chamber 8 to heat wire 1. The heater 10 may be of any conventional design whereby Wire 1 may be heated, for example, by radiation, electron bombardment, direct resistance heating or the like. Chamber 8 is also provided with cooling means 11 for cooling the heated or annealed wire 1. Cooling apparatus 11 may be composed of water-cooled rollers or any other conventional suitable cooling apparatus. The apparatus of the present invention may also include a means H for introducing a reducing gas such as hydrogen into the area of immersion bath 7 where the wire 1 enters and leaves the immersion bath 7.
A second embodiment of the present invention is illustrated in FIG. 2. In this particular embodiment of the invention supply spool 2 and guide roller 5 are mounted outside of the vacuum chamber 8. In addition to main conduit 9 employed to draw a vacuum on chamber 8, the apparatus includes a plurality of smaller conduits or ports 9 which assist in maintaining a vacuum in chamber 8 in the area where wire 1 is fed from supply spool 2 to the interior of vacuum chamber 8. In this embodiment of the invention the means H for supplying a reducing gas to the process includes a first means for supplying reducing gas to the interior of chamber 8 at the point where wire 1 enters immersion bath 7 and a second means for supplying reducing gas to a second point outside vacuum chamber 8 at the point where the wire 1 exits from the immersion bath 7.
In carrying out the process of the present invention the wire 1 is fed from supply spool 2 through vacuum chamber 8. Normally, the vacuum in vacuum chamber 8 will be maintained in the range of about 10- to l() torr (l torr being equivalent to a pressure of 1 mm. of mercury).
The wire 1 after being fed from supply spool 2 is heated by heater 10 to a temperature generally above about 700 C. to thereby anneal wire 1. In heating the surface by wire 1 by means of heater 10 in the vacuum maintained in vacuum chamber 8, a metallically clean surface is obtained free from oxides, grease, oil and the like; and possible gases dissolved in the metal are removed. If the wire 1 consists of steel with a high carbon content, the wire 1 will normally be heated to a temperature in the range of about 800 to 1000 C., e.g. 900 C., in order to obtain an austenite steel structure. In practice, it has been found that the heat treatment by means of heater 10 in vacuum chamber 8 produces a clean, metallic, thermically etched wire surface which may be coated with molten metal without the necessity of using the fiuxing treatment normally used in prior art processes.
The temperature of the wire 1 when it enters the metallizing bath is of great importance. If this temperature is too high, the danger exists that a reaction layer may be formed between the metal base of the wire 1 and the coating metal which is undesirably thick. In this case the coated wire 1 is likely to be brittle and when the coated wire is bent or folded small cracks may develop in the coating layer. Thus, a high degree of intermetallic combination or brittleness occurs when the temperature is too high so as to produce intermetallic diifusion.
On the other hand it is equally important that the temperature of the wire 1 is not too low when entering the immersion bath 7. Thus, if the temperature is too low the adhesion between the wire 1 and the coating metal will be inadequate.
It is for the above reasons that the heated annealed wire 1 is subsequently passed through cooler 11 which cools the temperature of wire 1 to the proper level. The particular temperature to which wire 1 is cooled in cooler 11 depends upon the nature of the substrate as well as the nature of the coating metal which is subsequently employed. The optimum temperature for any given combination of substrate and coating metal can be readily determined and should be selected to provide an operation in which the formation of a brittle reaction layer is minimized while at the same time producing an adequate adhesion between the wire 1 and the coating metal employed. If the wire 1 is made of a high carbon steel it is essential for proper annealing and isothermal hardening of the wire 1 to rapidly cool it down to a temperature in the range of about 400 to 600 C., e.g. 500 C. Thereafter, a controlled cooling of the wire 1 at a lower rate of cooling may be employed if desired, with respect to the particular type of coating metal which may subsequently be employed.
After the wire 1 has been annealed and cooled as described above it is passed into the immersion bath 7 containing a molten metal. The coating metals which can be most advantageously employed in the present invention, are metals with a low vapor pressure in the proximity of their melting temperature, such as, for example, aluminum, copper, tin and indium or alloys of these metals. The temperature of the coating metal in the bath 7 is preferably 'kept at a temperature level that is approximately 1 to 50 C. higher than the melting temperature. In this way only a small amount of metal will be lost through evaporation with the result that the amount of metal deposition on the walls of vacuum chamber 8 is minimized and further the best coating layers with the lowest percentages of intermetallic combinations are obtained. The following table lists the melting temperatures, the vapor pressure and evaporation speeds of a number of metals with low vapor pressures which may be utilized in the present invention:
. Approximate Melting evaporation temperature, Vapor speed in pressure, torr grams/sec. em.
1, 083 3. 2X1O- 7X10- 327 3. 4X 10- 10' Aluminum 660 1. 2X10- 10- In some cases, for example, with an aluminum coating it is advantageous to add a small percentage, e.g. 2 to 4 percent, of silicon to the immersion bath 7 in order to limit the formation of a reaction layer between the base and the coating metals. Other metals which have a. relative high vapor pressure, such as zinc, may be employed in the present invention but are less desirable than metals having lower vapor pressures. For example, zinc has a melting temperature of 420 C., a vapor pressure of 0.16 torr, and an evaporation speed in grams per second cm. of 10' In the practice of the present invention it is important that the wire 1, both before and during the dipping or coating in the bath 7, does not come into contact with the air. Thus, a strong reducing gas such as hydrogen may be injected under reduced pressure by means of a needle tap into the vacuum chamber 8 Where the wire enters and leaves the metallizing bath in order to reduce potential formation of oxide layers on the metal wire 1. Also, it is usually advantageous to place cooling elements between guide roller 5 and capstan 6 so that the coated wire is cooled down to a relatively low temperature before it is wound around capstan 6. This cooling assists in preventing deformation of the coated wire 1 in the subsequent processing steps.
A series of tests were carried out at different wire feeding speeds to develop data correlating the thickness of the coating layer in relation to the wire feed speed. These curves show a decrease initially of the coating layer thickness at increasing speed, and show that subsequently at a higher speed a thicker coating layer is produced because of the dragging effect of the molten metal on the wire passed through the immersion bath. The coating layers obtained by the process of the present invention are of a high quality with respect to adhesion of the metal coating and resistance to chipping, as well as uniformity of coating thickness.
In a series of tests a mild steel wire (i.e., a wire with a low carbon content; namely 0.10%) was passed through a bath filled with molten aluminum. The temperature of the molten aluminum was about 670 C. and the vacuum maintained above the bath was about 5 10- torr. The mild steel wire was first annealed at a temperature of about 850 C. and subsequently cooled down to a temperature of about 500 C. just before it was passed into the molten aluminum bath. In one of the tests, the bath contained 0.0% silicon; in a second test, the bath contained 2.0% silicon; and in a third test, the bath contained 4.0% silicon. All of the wires coated in the above experiments were found to have a qualitatively good coating layer.
The present invention carried out as described above was found to have the following advantages over the processes of the prior art. First, it was found that in carrying out the heat treatment under vacuum no oxidation occurred; and further, that any grease and the like evaporated at the elevated temperature and reduced pressure employed. Further it was found that the metal substrate after annealing remains in a thermically etched state and is in excellent condition for thorough moistening in the molten metal bath. Also, it was found that it was not necessary to pickle, rinse, flux and dry the wire after annealing and before metal coating. In addition, since it was found possible to eliminate the pickling step there is no longer any danger or special equipment involved in the removal of harmful gases. Further, since no fluxing process was required, no sludge deposits were produced in the metallizing bath. Also, in view of the fact that the metal substrate when entering the metal bath is at an elevated temperature in the range of 400 to 600 C., which is substantially higher than in conventional processes, an important energy gain was realized. Finally, in view of all the foregoing advantages, it has been found that the production and installation expenses for an apparatus for coating a metal substrate with molten metal are substantially decreased.
While the foregoing describes two specific embodiments of the present invention it will be understood that the present invention is subject to the various modifications within the capabilities of the person skilled in the art. Thus, the present invention can be practiced with a variety of designs without departing from the spirit and scope of the appended claims.
What is claimed is:
1. In a process for continuous coating of a metal substrate with a molten metal, the improvement which comprises annealing a substrate at an elevated temperature in a heating zone maintained under vacuum, cooling the annealed substrate in a cooling zone maintained under vacuum and coating the cooled annealed metal substrate 6 with a molten metal in an immersion zone maintained under vacuum.
2. The invention as defined by claim 1 in which said substrate is annealed at a temperature above 700 C. in said heating zone.
3. The invention as defined by claim 1 in which said substrate is a carbon steel wire which is annealed at a temperature in the range of about 700 to 1000 C. in said heating zone and cooled to a temperature in the range of about 400 to 600 C. in said cooling zone.
4. The invention as defined by claim 1 in which said molten metal is maintained at a temperature up to C. above its melting temperature.
5. The invention as defined by claim 1 in which a reducing gas is injected at reduced pressure into said immersion zone.
6. The invention as defined by claim 5 in which said reducing gas is hydrogen.
7. The invention defined by claim 1, in which said coating metal is a metal with a low vapor pressure at its melting temperature, said vapor pressure being no higher than about 3.2 10* torr.
References Cited UNITED STATES PATENTS 3,598,639 8/1971 'Hansson et al. 117-119 X 3,145,119 8/1964 Laforce et al. 117-1 14 R 3,010,844 11/1961 Klein et a1 117114 AX 1,343,842 6/1920 Piersol 117-119 2,761,793 9/1956 Brennan 11751 2,763,570 9/1956 Shepard et al. 11751 2,166,250 7/1939 Herman 1171 14 AX 3,130,068 4/1964 Whitley 117114 AX FOREIGN PATENTS 1,183,975 3/1970 Great Britain 117-1 14 A ALFRED L. LEAVITT, Primary Examiner J. R. BATTEN, 111., Assistant Examiner US. Cl. X.R.
117-114 R, 114 A, 114 B, 114 C, 119, 119.2; 118--50; 148-13
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL707006051A NL141933B (en) | 1970-04-24 | 1970-04-24 | METHOD OF COVERING A LONG-STRETCHED METAL OBJECT WITH METAL, AND OBJECTS COATED ACCORDING TO THIS METHOD. |
Publications (1)
Publication Number | Publication Date |
---|---|
US3728144A true US3728144A (en) | 1973-04-17 |
Family
ID=19809952
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00134738A Expired - Lifetime US3728144A (en) | 1970-04-24 | 1971-04-16 | Method for coating metal substrates with molten metal |
Country Status (7)
Country | Link |
---|---|
US (1) | US3728144A (en) |
BE (1) | BE764601A (en) |
DE (1) | DE2119920C3 (en) |
FR (1) | FR2086302B1 (en) |
GB (1) | GB1325941A (en) |
LU (1) | LU63017A1 (en) |
NL (1) | NL141933B (en) |
Cited By (20)
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US3907965A (en) * | 1973-06-28 | 1975-09-23 | Nippon Kokan Kk | Method of preventing surface flaws on steel strip produced in pre-treatment furnace of continuous hot-dipping process |
US3914466A (en) * | 1974-01-25 | 1975-10-21 | Matsushita Electric Ind Co Ltd | Method for coating an article |
US4053663A (en) * | 1972-08-09 | 1977-10-11 | Bethlehem Steel Corporation | Method of treating ferrous strand for coating with aluminum-zinc alloys |
US4478892A (en) * | 1983-03-16 | 1984-10-23 | National Steel Corporation | Method of and apparatus for hot dip coating of steel strip |
US4675214A (en) * | 1986-05-20 | 1987-06-23 | Kilbane Farrell M | Hot dip aluminum coated chromium alloy steel |
US4800135A (en) * | 1986-05-20 | 1989-01-24 | Armco Inc. | Hot dip aluminum coated chromium alloy steel |
US5480731A (en) * | 1992-03-27 | 1996-01-02 | The Louis Berkman Company | Hot dip terne coated roofing material |
US5491036A (en) * | 1992-03-27 | 1996-02-13 | The Louis Berkman Company | Coated strip |
US5695822A (en) * | 1993-04-05 | 1997-12-09 | The Louis Berkman Company | Method for coating a metal strip |
US6016596A (en) * | 1997-05-21 | 2000-01-25 | Rodgers; John | Mounting apparatus and method of use |
US6080497A (en) * | 1992-03-27 | 2000-06-27 | The Louis Berkman Company | Corrosion-resistant coated copper metal and method for making the same |
US20030061837A1 (en) * | 2001-10-01 | 2003-04-03 | Swain Robert F. | Method and apparatus for removing polymeric coatings from optical fiber in a non-oxidizing environment |
US20030062070A1 (en) * | 2001-10-01 | 2003-04-03 | Swain Robert F. | Method and apparatus for removing polymeric coatings from optical fiber |
WO2003078676A1 (en) * | 2002-03-18 | 2003-09-25 | Karl Merz | Method and device for the alfin processing of components |
US6652990B2 (en) | 1992-03-27 | 2003-11-25 | The Louis Berkman Company | Corrosion-resistant coated metal and method for making the same |
US6794060B2 (en) | 1992-03-27 | 2004-09-21 | The Louis Berkman Company | Corrosion-resistant coated metal and method for making the same |
US20040214029A1 (en) * | 1992-03-27 | 2004-10-28 | The Louis Berkman Company, An Ohio Corporation | Corrosion-resistant coated copper and method for making the same |
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Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6179755A (en) * | 1984-09-28 | 1986-04-23 | Nisshin Steel Co Ltd | Continuous plating device in common use for hot dipping and vacuum deposition plating |
FR2720079B1 (en) * | 1994-05-19 | 1996-06-21 | Lorraine Laminage | Process for coating aluminum by hot quenching a part, in particular a strip, of steel containing at least 0.1% by weight of manganese, in particular of stainless and / or alloyed steel. |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2111826A (en) * | 1935-12-09 | 1938-03-22 | Northwestern Barb Wire Company | Galvanizing process |
GB676198A (en) * | 1946-07-31 | 1952-07-23 | Michel Alferieff | Process for coating metallic objects with other metals |
-
1970
- 1970-04-24 NL NL707006051A patent/NL141933B/en unknown
-
1971
- 1971-03-22 BE BE764601A patent/BE764601A/en unknown
- 1971-04-16 US US00134738A patent/US3728144A/en not_active Expired - Lifetime
- 1971-04-16 FR FR717113527A patent/FR2086302B1/fr not_active Expired
- 1971-04-20 LU LU63017D patent/LU63017A1/xx unknown
- 1971-04-23 DE DE2119920A patent/DE2119920C3/en not_active Expired
- 1971-04-23 GB GB1120271*[A patent/GB1325941A/en not_active Expired
Cited By (36)
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US4800135A (en) * | 1986-05-20 | 1989-01-24 | Armco Inc. | Hot dip aluminum coated chromium alloy steel |
US6794060B2 (en) | 1992-03-27 | 2004-09-21 | The Louis Berkman Company | Corrosion-resistant coated metal and method for making the same |
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US5520964A (en) * | 1992-03-27 | 1996-05-28 | The Louis Berkman Company | Method of coating a metal strip |
US5616424A (en) * | 1992-03-27 | 1997-04-01 | The Louis Berkman Company | Corrosion-resistant coated metal strip |
US5667849A (en) * | 1992-03-27 | 1997-09-16 | The Louis Berkman Company | Method for coating a metal strip |
US5491036A (en) * | 1992-03-27 | 1996-02-13 | The Louis Berkman Company | Coated strip |
US20070104975A1 (en) * | 1992-03-27 | 2007-05-10 | The Louis Berkman Company | Corrosion-resistant coated copper and method for making the same |
US6080497A (en) * | 1992-03-27 | 2000-06-27 | The Louis Berkman Company | Corrosion-resistant coated copper metal and method for making the same |
US20070023111A1 (en) * | 1992-03-27 | 2007-02-01 | The Louis Berkman Company, A Corporation Of Ohio | Corrosion-resistant fuel tank |
US7045221B2 (en) | 1992-03-27 | 2006-05-16 | The Louis Berkman Company | Corrosion-resistant coated copper and method for making the same |
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US6016596A (en) * | 1997-05-21 | 2000-01-25 | Rodgers; John | Mounting apparatus and method of use |
US7003985B2 (en) | 2001-10-01 | 2006-02-28 | Swain Robert F | Method and apparatus for removing polymeric coatings from optical fiber in a non-oxidizing environment |
US20030062070A1 (en) * | 2001-10-01 | 2003-04-03 | Swain Robert F. | Method and apparatus for removing polymeric coatings from optical fiber |
US20030061837A1 (en) * | 2001-10-01 | 2003-04-03 | Swain Robert F. | Method and apparatus for removing polymeric coatings from optical fiber in a non-oxidizing environment |
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US9991410B2 (en) | 2011-09-29 | 2018-06-05 | Neturen Co., Ltd. | Method and apparatus for manufacturing lead wire for solar cell |
US20180042394A1 (en) * | 2015-02-23 | 2018-02-15 | Agro Holding Gmbh | Method for producing an upholstery spring, upholstery spring, mattress, and upholstered furniture |
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Also Published As
Publication number | Publication date |
---|---|
LU63017A1 (en) | 1971-08-26 |
NL7006051A (en) | 1971-10-26 |
DE2119920B2 (en) | 1974-02-14 |
DE2119920C3 (en) | 1974-10-03 |
DE2119920A1 (en) | 1971-11-11 |
FR2086302A1 (en) | 1971-12-31 |
FR2086302B1 (en) | 1974-02-15 |
GB1325941A (en) | 1973-08-08 |
NL141933B (en) | 1974-04-16 |
BE764601A (en) | 1971-08-16 |
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