US3884729A - Method of providing an aluminum coating on a steel substrate - Google Patents

Method of providing an aluminum coating on a steel substrate Download PDF

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US3884729A
US3884729A US411846A US41184673A US3884729A US 3884729 A US3884729 A US 3884729A US 411846 A US411846 A US 411846A US 41184673 A US41184673 A US 41184673A US 3884729 A US3884729 A US 3884729A
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substrate
powder
aluminium
coating
iron
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US411846A
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Albert Edward Jackson
Ernest Wynne Williams
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British Steel Corp
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British Steel Corp
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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
    • C23C10/00Solid state diffusion of only metal elements or silicon into metallic material surfaces
    • C23C10/28Solid state diffusion of only metal elements or silicon into metallic material surfaces using solids, e.g. powders, pastes
    • C23C10/34Embedding in a powder mixture, i.e. pack cementation
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/4998Combined manufacture including applying or shaping of fluent material
    • Y10T29/49982Coating
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12014All metal or with adjacent metals having metal particles
    • Y10T428/12028Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, etc.]
    • Y10T428/12063Nonparticulate metal component
    • Y10T428/12139Nonmetal particles in particulate component
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12771Transition metal-base component
    • Y10T428/12861Group VIII or IB metal-base component
    • Y10T428/12951Fe-base component
    • Y10T428/12958Next to Fe-base component
    • Y10T428/12965Both containing 0.01-1.7% carbon [i.e., steel]

Definitions

  • ABSTRACT A method of providing a surface of a steel substrate with an aluminum coating, the said method comprising coating the said surface of the steel substrate with a layer of metal, coating the said metal layer with a layer containing aluminium powder, the aluminium powder forming an alloy with the steel substrate at a predetermined elevated temperature, compacting the said metal and powder layers to the substrate, effecting a cold reduction, and effecting a subsequent annealing heat treatment to make the metal and powder layers adhere tightly to the substrate, and thus provide the substrate with the said aluminium coating, the metal layer serving to control nucleation of the said alloy which is formed at the said predetermined elevated temperature.
  • the annealing temperature is limited by the fact that if a certain temperature is exceeded, then nucleation and growth of a brittle, intermetallic, iron-aluminium alloy will occur and the bond between the aluminium coating and the steel substrate will deteriorate.
  • This temperature is dependent upon the chemical composition of the steel substrate and can be as low as 500C in the case of some rimming steels. However, it is in practice necessary for the annealing temperature to exceed 500C if the annealing is to be adequate to compensate for the effects of the cold reduction.
  • a method of providing a surface of a steel substrate with an aluminium coating comprising coating the said surface of the steel substrate with a layer of metal, coating the said metal layer with a layer of or containing aluminium powder, the aluminium powder forming an alloy with the steel substrate at a predetermined elevated temperature, compacting the said metal and powder layers to the substrate, effecting a cold reduction, and effecting a subsequent annealing heat treatment to make the metal and powder layers adhere tightly to the substrate and thus provide the substrate with the said aluminium coating, the metal layer serving to control nucleation of the said alloy which is formed at the said predetermined elevated temperature.
  • the compacted substrate after compacting the said metal and powder layers and before effecting the cold reduction, the compacted substrate may be subjected to an additional heat treatment.
  • the provision of the said metal layer which is preferably composed of iron, retards the nucleation of an iron/aluminium alloy layer by raising the temperature below which little or no nucleation occurs.
  • nucleation when nucleation commences, the growth of the alloy from given nucleates is very rapid due to the fast rate of reaction at the raised nucleation temperature. As a result, the risk of blistering and delamination may be reduced.
  • nucleation appears to be controlled such that the alloy grows in a toothy pattern into the aluminium layer, thereby promoting adhesion of the layers to each other.
  • the present invention enables one to produce in a single continuous manufacturing process a cold reucked aluminium coated steel substrate in which the risk of delamination of the aluminium coating is reduced.
  • the gauge of the so-coated substrate preferably undergoes a reduction of at least 30 percent in the course of the said cold reduction.
  • the reduction in gauge may be substantially in the range of 50 to 90 percent.
  • the original substrate may have a gauge in the range 0.1 inch to 0.04 inch.
  • the annealing heat treatment may be a re-crystallisation anneal which is effected at a temperature within the range of 500 to 550C.
  • compaction is effected by passing the coated substrate between a pair of rollers, and the substrate, prior to passing between the rollers, may be wetted with a liquid which reduces the extent to which the said rollers dislodge the aluminium powder.
  • the metal layer is preferably an electrolytically deposited layer of iron.
  • the powder layer may be made up of aluminium particles which are applied to the substrate in an electrostatically charged condition, the average particle size of the aluminium particles not exceeding 40 microns.
  • the powder layer containing the aluminium powder may contain aluminium powder whose average particle size does not exceed 40 microns and also contains a finely divided silicious material which causes the aluminium powder to flow substantially more readily than it would in the absence of the silicious material, the silicious material constituting not more than 0.5 percent by weight of said powder layer.
  • the silicious material may comprise particles of silica each of which has been provided with an hydrophobic organic coating.
  • the powder layer may be applied to the steel substrate in the form of a slurry.
  • This slurry may be dried before it is compacted to the substrate.
  • the slurry may contain silica.
  • the slurry may contain a water soluble cellulose ether.
  • the invention also comprises a steel substrate provided with an aluminium coating by the method set forth above.
  • a mild steel strip to be coated having a gauge in the range 0.] inch to 0.04 inch, is wound from a roll thereof and passes at a speed of up to 300 feet per minute through a de-greasing bath where the strip is degreased by a conventional de-greasing liquid. lt is then rinsed in cold water whereafter it is pickled in pickling baths.
  • the pickling baths may contain dilute nitric acid, eg they may contain 5 percent by weight nitric acid, and in addition may contain 25 grams per litre of urea so as to inhibit the accumulation in the baths of nitrous acid and oxides of nitrogen which if allowed to accumulate would render the baths inactive.
  • the pickling baths may contain sulphuric or hydrochloric acid.
  • the strip is then rinsed, whereafter it passes successively to two electrolytic plating baths where layers of iron are electrolytically applied to both the opposite surfaces of the strip.
  • Each of the electrolytic plating baths contains an aqueous solution of an iron-salt such as ferrous chloride or ferrous sulphate, when the pickling baths contain hydrochloric acid or sulphuric acid then the waste pickle liquor therefrom may be employed in the electroplating baths.
  • the strip After passing through the electro-plating baths the strip is rinsed and is then dried. The strip then passes to a powder coating station where one surface of the strip has a solution of sodium (or potassium) silicate sprayed onto it, e.g., in a quantity amounting to 1.5 cc per square foot of the strip, the concentration of the sodium silicate in the said solution being 3 grams per litre.
  • a solution of sodium (or potassium) silicate sprayed onto it e.g., in a quantity amounting to 1.5 cc per square foot of the strip, the concentration of the sodium silicate in the said solution being 3 grams per litre.
  • the strip then passes beneath a feed tray which is arranged to receive a powdered coatant from a hopper.
  • the feed tray has vibratory pulses imparted to it, to cause the particles of powdered coatant to move thereover and to fall onto the adjacent surface of the strip.
  • the powdered coatant in the hopper consists of a mixture of aluminium powder and silica particles, the silica particles constituting 0.001 percent by weight of the mixture.
  • the aluminium powder may pass a 300 mesh sieve and have an average particle size which does not exceed 40 microns, and preferably does not exceed 30 microns.
  • the average particle size of the aluminium powder may be 20 microns.
  • Each of the particles of silica has been provided with an hydrophobic organic coating, e.g., of dimethyl chlorosilane.
  • an organic coating e.g., of dimethyl chlorosilane.
  • silica particles are available commercially under the Trade Names Silica D17" and Aerosil R972.”
  • the average particle size of the silica particles should preferably not exceed 30 millimicrons and may for example be 22 millimicrons, while the bulk density of the silica should preferably not exceed 40 grams per litre and may for example be 30 grams per litre.
  • the apparatus constituted by the said feed tray and hopper may for example be as disclosed in British Specification No. 1,094,157 although of course this apparatus is suitable for use with the powdered coatant described above only because the latter comprises the said silica particles.
  • the strip then passes over further rollers so as to reverse the one of its surfaces which is uppermost.
  • the non-coated surface thus now passes beneath a powder coating station which corresponds to the powder coating station described above, and which is arranged to wet the last-mentioned surface with sodium or potassium silicate solution.
  • the last-mentioned surface then passes under a vibrating feed tray which receives the said powdered coatant from a hopper.
  • the strip after leaving the last-mentioned hopper, has been both wetted and coated on both of its opposite surfaces.
  • the strip then passes through drying stations each of which incorporate a high frequency heater.
  • the coated strip is then sprayed at the rate of 3 cc per square foot with a 0.2 percent colloidal solution of sodium carboxymethylcellulose and is thereafter dried, the strip then being passed between a pair of rollers of a rolling mill which compacts the layers of aluminium powder and iron to the steel substrate.
  • the compacted strip is then coiled for a sintering heat treatment in which the aluminium and iron layers are caused to adhere tightly to each other and to the steel substrate and thus provide the latter with an aluminium coating.
  • the heat treatment may comprise heating the coil in air for to hours at 300 to 500C, preferably 350C, whereby bonding and sintering occurs,
  • the so-coated steel substrate is then subjected to a cold reduction in gauge in the range of 50 to 70 percent so as to reduce the coated substrate to its final gauge, this being then followed by an annealing heat treatment comprising a re-crystallisation anneal e.g., for 24 hours, at a temperature in the range of 500 to 550C.
  • this annealing heat treatment may be such as to effect the sintering and bonding referred to above, in which case the said sintering heat treatment, which is effected after compaction and coiling may be omitted.
  • the length of substrate is, of course, correspondingly increased.
  • the cold reduction is one of 50 percent, it is necessary to provide an aluminium powder layer having double the thickness required (which may be 0.0015 inch), of the final material.
  • a hot rolled mild steel strip to be coated having a gauge of 2.19 mm and a width of 1,000 mm, is wound from a 10 ton coil thereof and de-greased in a conventional hot alkaline de-greasing liquid. It is then rinsed in cold water, after which it is pickled in a pickling bath containing 5 percent by volume of cold hydrochloric acid.
  • the strip is then rinsed whereafter it passes to an electrolytic plating bath where both the opposite surfaces of the strip are simultaneously plated with 1.75 micron layers of iron.
  • the electrolytic plating bath comprises an aqueous solution containing grams per litre of ferrous chloride tetrahydrate and 10 grams per litre of tri-sodium citrate, the bath being operated at 50C and 2,700 amps per square metre.
  • the electroplated strip is then rinsed and dried.
  • the top surface of the electroplated strip is now wetted with 5.0 cc per square metre of a solution containing 8 grams per litre of sodium silicate (e.g., the sodium silicate commercially available as Crosfields 100 alk grade).
  • the wetted top surface of the electroplated strip is now coated with 250 grams per square metre of aluminium powder having an average particle size of 25 microns. the powder being applied from a vibrating table through a vibrating wire grid which is electrostatically charged to a voltage of 20 Kv. The passage of the powder particles through the grid causes the particles to be electrostatically charged and thus mutually repelled and then attracted to the strip, which is earthed, to give a uniform, dense coating.
  • the electroplated strip whose top surface has been so wetted and coated is then passed around rollers to reverse its direction of movement, and the opposite side of the electroplated strip is then similarly wetted with sodium silicate solution and electrostatically coated with a layer of aluminium powder.
  • the coated strip is then passed through a radiant gasfired oven to remove moisture, but the aluminium powder continues to adhere to the underside of the coated strip because the sodium silicate acts as a binder.
  • the coated strip then passes through a rolling mill where the powder is compacted to the electroplated steel substrate to form a coherent foil.
  • This strip is then recoiled and heat-treated in air in a conventional annealing furnace for 16 hours at 350C. It is then cold reduced to a finished gauge of 0.55 mm on a reversing mill, annealed at 525C for 16 hours and finally temper rolled.
  • EXAMPLE III A mild steel panel, having a gauge in the range of 0.1 inch to 0.04 inch, is degreased, rinsed in cold Water,
  • the panel is then electroplated with iron in electroplating baths containing an aqueous solution of an iron salt such as ferrous chloride or ferrous sulphate. Thereafterthe panel is rinsed and then dried.
  • an iron salt such as ferrous chloride or ferrous sulphate.
  • the panel is then immersed in and withdrawn at a steady rate from a bath containing an aqueous aluminium powder slurry formed from aluminium powder, of a particle size not exceeding 300 mesh per linear inch, the slurry having the following composition:
  • Aluminium Powder 400 gms Water 300 gms Na O.2 SiO 1.7 gms Nl-LNO; 2.4 gms HNO up to pH 9.0
  • the bath thus contains precipated silica in an amount sufficient to give buoyancy to the slurry and confer a degree of thixotropy thereto.
  • precipated silica in an amount sufficient to give buoyancy to the slurry and confer a degree of thixotropy thereto.
  • the coated panel is now dried at a temperature of 100C and is passed between a pair of rollers of a rolling mill which compacts the aluminium powder and electroplated iron to the steel plate, the passage through the said rolling mill producing a reduction in thickness of 5 to 7 percent.
  • the coated panel is then heated in air at 350C, whereby bonding and sintering occur, after which the coated panel is subjected to a cold reduction to produce a final foil thickness in the range 38 to 60 microns (0.0015 inch to 0.0023 inch). Finally, the product is given a re-crystallization anneal for 24 hours at a temperature in the range of 500 to 550C.
  • the withdrawal of the panel from the slurry bath may be constituted by vertical withdrawal.
  • the slurry instead of immersing the panel in a slurry bath, the slurry, mentioned above may be applied to the panel by a reverse roller coater as in the conventional paint coating of metal strip.
  • EXAMPLE IV The procedure is the same as in Example 111 except that the panel, instead of being immersed in a slurry bath, is sprayed with the slurry by the use of compressed air.
  • the slurry employed is thinner i.e. employs more water, than that of Example III, and may for example, be as follows:
  • Such a slurry may be used to build up a coating of any desired thickness, using known spray painting technology.
  • EXAMPLE V The procedure is the same as in Example Ill except that the panel instead of being immersed in a slurry bath, is curtain coated, at a speed of up to 240 ft/minute, with a slurry of the following composition:
  • the slurry also preferably includes a surfactant such, for example, as an alkyl aryl sulphonate.
  • the inhibitor used instead of being sodium dichromate, could be sodium silicate, sodium chromate, or di-ammonium hydrogen phosphate.
  • the slurry is made up by first dispersing the water soluble cellulose ether e.g., sodium carboxy methyl cellulose, in the water, and leaving it for an appropriate swelling period. After this the inhibitor is first added, and subsequently the aluminium powder (and the surfactant, if employed).
  • water soluble cellulose ether e.g., sodium carboxy methyl cellulose
  • a method of providing a surface of a steel substrate with an aluminium coating comprising electroplating the said surface of the steel substrate with a layer of iron, coating the iron layer with a layer containing aluminium powder, and compacting the said iron and powder layers to the substrate, the improvement which consists of subsequently effecting a cold reduction which reduces the gauge of the so-called substrate by at least 30 percent, and effecting a subsequent recrystallisation annealing heat treatment to make the iron and powder layers adhere tightly to the substrate.
  • compaction is effected by passing the coated substrate between a pair of rollers, the substrate, prior to passing between the rollers, being wetted with a liquid which reduces the extent to which the said rollers dislodge the aluminium powder.
  • the powder layer is made up of aluminium particles which are applied to the substrate in an electrostatically charged condition, the average particle size of the aluminium particles not exceeding 40 microns.
  • the powder layer contains aluminium powder whose average particle size does not exceed 40 microns and also contains a finely divided silicious material which causes the aluminium powder to flow substantially more readily than it would in the absence of the silicious material, the silicious material constituting not more than 0.5 percent by weight of the said powder layer.

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Abstract

A method of providing a surface of a steel substrate with an aluminum coating, the said method comprising coating the said surface of the steel substrate with a layer of metal, coating the said metal layer with a layer containing aluminium powder, the aluminium powder forming an alloy with the steel substrate at a predetermined elevated temperature, compacting the said metal and powder layers to the substrate, effecting a cold reduction, and effecting a subsequent annealing heat treatment to make the metal and powder layers adhere tightly to the substrate, and thus provide the substrate with the said aluminium coating, the metal layer serving to control nucleation of the said alloy which is formed at the said predetermined elevated temperature.

Description

United States Patent Jackson et al.
METHOD OF PROVIDING AN ALUMINUM COATING ON A STEEL SUBSTRATE Inventors: Albert Edward Jackson,
Gwernaffield Mold; Ernest Wynne Williams, Mold, both of Wales British Steel Corporation, London, England Filed: Nov. 1, 1973 Appl. No.: 411,846
Assignee:
Foreign Application Priority Data Nov. 3, 1972 United Kingdom 50773/72 US. Cl l48/1l.5 A; 29/192 CP; 29/196.1; 29/196.2; 29/197; 29/527.2; 75/208 CS; 117/22; 204/37 R; 204/38 S Int. Cl. C2ld B22f 7/00 Field of Search 204/37 R, 385, 117/201, 117/215, 217, 230, 29, 22; 29/192 GP, 194, 196.1, 196.2, 197, 527.2; 148/11.5 A;
References Cited UNITED STATES PATENTS Jost 75/201 3,597,172 8/1971 Bungardt et al. 29/194 3,661,612 5/1972 Jackson et al. 117/22 3,717,513 2/1973 Adenis l48/ll.5 A
3,755,090 8/1973 Jackson et al. .1 204/34 3,827,140 8/1974 Yamagishi et al. 29/487 Primary Examiner-John H. Mack Assistant ExaminerAaron Weisstuch Attorney, Agent, or Firm-Cushman, Darby & Cushman 5 7] ABSTRACT A method of providing a surface of a steel substrate with an aluminum coating, the said method comprising coating the said surface of the steel substrate with a layer of metal, coating the said metal layer with a layer containing aluminium powder, the aluminium powder forming an alloy with the steel substrate at a predetermined elevated temperature, compacting the said metal and powder layers to the substrate, effecting a cold reduction, and effecting a subsequent annealing heat treatment to make the metal and powder layers adhere tightly to the substrate, and thus provide the substrate with the said aluminium coating, the metal layer serving to control nucleation of the said alloy which is formed at the said predetermined elevated temperature.
13 Claims, No Drawings METHOD OF PROVIDING AN ALUMINUM COATING ON A STEEL SUBSTRATE This invention concerns a method of providing an aluminium coating on a steel substrate.
lfa conventional aluminium coated steel substrate, in which the substrate has aluminium directly coated thereon, is cold reduced and recrystallisation annealed, the annealing temperature is limited by the fact that if a certain temperature is exceeded, then nucleation and growth of a brittle, intermetallic, iron-aluminium alloy will occur and the bond between the aluminium coating and the steel substrate will deteriorate. This temperature is dependent upon the chemical composition of the steel substrate and can be as low as 500C in the case of some rimming steels. However, it is in practice necessary for the annealing temperature to exceed 500C if the annealing is to be adequate to compensate for the effects of the cold reduction.
According to one particular aspect of the present invention, there is provided a method of providing a surface of a steel substrate with an aluminium coating, the said method comprising coating the said surface of the steel substrate with a layer of metal, coating the said metal layer with a layer of or containing aluminium powder, the aluminium powder forming an alloy with the steel substrate at a predetermined elevated temperature, compacting the said metal and powder layers to the substrate, effecting a cold reduction, and effecting a subsequent annealing heat treatment to make the metal and powder layers adhere tightly to the substrate and thus provide the substrate with the said aluminium coating, the metal layer serving to control nucleation of the said alloy which is formed at the said predetermined elevated temperature.
lf desired, after compacting the said metal and powder layers and before effecting the cold reduction, the compacted substrate may be subjected to an additional heat treatment.
We think that the provision of the said metal layer, which is preferably composed of iron, retards the nucleation of an iron/aluminium alloy layer by raising the temperature below which little or no nucleation occurs.
We think that when nucleation commences, the growth of the alloy from given nucleates is very rapid due to the fast rate of reaction at the raised nucleation temperature. As a result, the risk of blistering and delamination may be reduced. Thus the nucleation appears to be controlled such that the alloy grows in a toothy pattern into the aluminium layer, thereby promoting adhesion of the layers to each other.
Thus the present invention enables one to produce in a single continuous manufacturing process a cold re duced aluminium coated steel substrate in which the risk of delamination of the aluminium coating is reduced.
The gauge of the so-coated substrate preferably undergoes a reduction of at least 30 percent in the course of the said cold reduction. Thus the reduction in gauge may be substantially in the range of 50 to 90 percent.
The original substrate may have a gauge in the range 0.1 inch to 0.04 inch.
The annealing heat treatment may be a re-crystallisation anneal which is effected at a temperature within the range of 500 to 550C.
Preferably compaction is effected by passing the coated substrate between a pair of rollers, and the substrate, prior to passing between the rollers, may be wetted with a liquid which reduces the extent to which the said rollers dislodge the aluminium powder.
The metal layer is preferably an electrolytically deposited layer of iron.
The powder layer may be made up of aluminium particles which are applied to the substrate in an electrostatically charged condition, the average particle size of the aluminium particles not exceeding 40 microns.
Alternatively, the powder layer containing the aluminium powder may contain aluminium powder whose average particle size does not exceed 40 microns and also contains a finely divided silicious material which causes the aluminium powder to flow substantially more readily than it would in the absence of the silicious material, the silicious material constituting not more than 0.5 percent by weight of said powder layer. Thus the silicious material may comprise particles of silica each of which has been provided with an hydrophobic organic coating.
Yet again, the powder layer may be applied to the steel substrate in the form of a slurry. This slurry may be dried before it is compacted to the substrate.
The slurry may contain silica.
Alternatively, the slurry may contain a water soluble cellulose ether.
The invention also comprises a steel substrate provided with an aluminium coating by the method set forth above.
The invention is illustrated in the following Examples.
EXAMPLE I A mild steel strip to be coated, having a gauge in the range 0.] inch to 0.04 inch, is wound from a roll thereof and passes at a speed of up to 300 feet per minute through a de-greasing bath where the strip is degreased by a conventional de-greasing liquid. lt is then rinsed in cold water whereafter it is pickled in pickling baths. The pickling baths may contain dilute nitric acid, eg they may contain 5 percent by weight nitric acid, and in addition may contain 25 grams per litre of urea so as to inhibit the accumulation in the baths of nitrous acid and oxides of nitrogen which if allowed to accumulate would render the baths inactive. Alternatively, the pickling baths may contain sulphuric or hydrochloric acid.
The strip is then rinsed, whereafter it passes successively to two electrolytic plating baths where layers of iron are electrolytically applied to both the opposite surfaces of the strip. Each of the electrolytic plating baths contains an aqueous solution of an iron-salt such as ferrous chloride or ferrous sulphate, when the pickling baths contain hydrochloric acid or sulphuric acid then the waste pickle liquor therefrom may be employed in the electroplating baths.
After passing through the electro-plating baths the strip is rinsed and is then dried. The strip then passes to a powder coating station where one surface of the strip has a solution of sodium (or potassium) silicate sprayed onto it, e.g., in a quantity amounting to 1.5 cc per square foot of the strip, the concentration of the sodium silicate in the said solution being 3 grams per litre.
The strip then passes beneath a feed tray which is arranged to receive a powdered coatant from a hopper. The feed tray has vibratory pulses imparted to it, to cause the particles of powdered coatant to move thereover and to fall onto the adjacent surface of the strip.
The powdered coatant in the hopper consists of a mixture of aluminium powder and silica particles, the silica particles constituting 0.001 percent by weight of the mixture. The aluminium powder may pass a 300 mesh sieve and have an average particle size which does not exceed 40 microns, and preferably does not exceed 30 microns. For example, the average particle size of the aluminium powder may be 20 microns.
Each of the particles of silica has been provided with an hydrophobic organic coating, e.g., of dimethyl chlorosilane. Thus very pure silica produced by flame hydrolysis may be reacted in an inert atmosphere at 400C with dimethyl chlorosilane and steam so as to produce such coated silica particles. Such coated silica particles are available commercially under the Trade Names Silica D17" and Aerosil R972."
The average particle size of the silica particles should preferably not exceed 30 millimicrons and may for example be 22 millimicrons, while the bulk density of the silica should preferably not exceed 40 grams per litre and may for example be 30 grams per litre.
The apparatus constituted by the said feed tray and hopper may for example be as disclosed in British Specification No. 1,094,157 although of course this apparatus is suitable for use with the powdered coatant described above only because the latter comprises the said silica particles.
The strip then passes over further rollers so as to reverse the one of its surfaces which is uppermost. The non-coated surface thus now passes beneath a powder coating station which corresponds to the powder coating station described above, and which is arranged to wet the last-mentioned surface with sodium or potassium silicate solution. The last-mentioned surface then passes under a vibrating feed tray which receives the said powdered coatant from a hopper. As will be appreciated, the strip, after leaving the last-mentioned hopper, has been both wetted and coated on both of its opposite surfaces.
The strip then passes through drying stations each of which incorporate a high frequency heater.
The coated strip is then sprayed at the rate of 3 cc per square foot with a 0.2 percent colloidal solution of sodium carboxymethylcellulose and is thereafter dried, the strip then being passed between a pair of rollers of a rolling mill which compacts the layers of aluminium powder and iron to the steel substrate.
The spraying of the strip with the sodium carboxymethylcellulose reduces the extent to which the said rollers would otherwise dislodge the aluminium powder. Thus there is a reduced tendency for banks of dislodged powder to build up immediately ahead of the rollers and thereby prevent the strip being moved at high speeds.
The compacted strip is then coiled for a sintering heat treatment in which the aluminium and iron layers are caused to adhere tightly to each other and to the steel substrate and thus provide the latter with an aluminium coating. Thus the heat treatment may comprise heating the coil in air for to hours at 300 to 500C, preferably 350C, whereby bonding and sintering occurs,
The so-coated steel substrate is then subjected to a cold reduction in gauge in the range of 50 to 70 percent so as to reduce the coated substrate to its final gauge, this being then followed by an annealing heat treatment comprising a re-crystallisation anneal e.g., for 24 hours, at a temperature in the range of 500 to 550C.
If desired, this annealing heat treatment may be such as to effect the sintering and bonding referred to above, in which case the said sintering heat treatment, which is effected after compaction and coiling may be omitted.
In the course of the said cold reduction, the length of substrate is, of course, correspondingly increased.
Thus assuming that the cold reduction is one of 50 percent, it is necessary to provide an aluminium powder layer having double the thickness required (which may be 0.0015 inch), of the final material.
EXAMPLE II A hot rolled mild steel strip to be coated, having a gauge of 2.19 mm and a width of 1,000 mm, is wound from a 10 ton coil thereof and de-greased in a conventional hot alkaline de-greasing liquid. It is then rinsed in cold water, after which it is pickled in a pickling bath containing 5 percent by volume of cold hydrochloric acid.
The strip is then rinsed whereafter it passes to an electrolytic plating bath where both the opposite surfaces of the strip are simultaneously plated with 1.75 micron layers of iron. The electrolytic plating bath comprises an aqueous solution containing grams per litre of ferrous chloride tetrahydrate and 10 grams per litre of tri-sodium citrate, the bath being operated at 50C and 2,700 amps per square metre. The electroplated strip is then rinsed and dried.
The top surface of the electroplated strip is now wetted with 5.0 cc per square metre of a solution containing 8 grams per litre of sodium silicate (e.g., the sodium silicate commercially available as Crosfields 100 alk grade). The wetted top surface of the electroplated strip is now coated with 250 grams per square metre of aluminium powder having an average particle size of 25 microns. the powder being applied from a vibrating table through a vibrating wire grid which is electrostatically charged to a voltage of 20 Kv. The passage of the powder particles through the grid causes the particles to be electrostatically charged and thus mutually repelled and then attracted to the strip, which is earthed, to give a uniform, dense coating.
The electroplated strip whose top surface has been so wetted and coated is then passed around rollers to reverse its direction of movement, and the opposite side of the electroplated strip is then similarly wetted with sodium silicate solution and electrostatically coated with a layer of aluminium powder.
The coated strip is then passed through a radiant gasfired oven to remove moisture, but the aluminium powder continues to adhere to the underside of the coated strip because the sodium silicate acts as a binder. The coated strip then passes through a rolling mill where the powder is compacted to the electroplated steel substrate to form a coherent foil.
This strip is then recoiled and heat-treated in air in a conventional annealing furnace for 16 hours at 350C. It is then cold reduced to a finished gauge of 0.55 mm on a reversing mill, annealed at 525C for 16 hours and finally temper rolled.
EXAMPLE III A mild steel panel, having a gauge in the range of 0.1 inch to 0.04 inch, is degreased, rinsed in cold Water,
and pickled in nitric. acid.. The panel is then electroplated with iron in electroplating baths containing an aqueous solution of an iron salt such as ferrous chloride or ferrous sulphate. Thereafterthe panel is rinsed and then dried.
The panel is then immersed in and withdrawn at a steady rate from a bath containing an aqueous aluminium powder slurry formed from aluminium powder, of a particle size not exceeding 300 mesh per linear inch, the slurry having the following composition:
Aluminium Powder 400 gms Water 300 gms Na O.2 SiO 1.7 gms Nl-LNO; 2.4 gms HNO up to pH 9.0
Total volume of above slurry 520 mls. The bath thus contains precipated silica in an amount sufficient to give buoyancy to the slurry and confer a degree of thixotropy thereto. By varying the quantities of aluminium powder and silica in the slurry, different viscosities of slurry can be achieved, and this can in turn control the thickness of the coating applied to the panel.
The coated panel is now dried at a temperature of 100C and is passed between a pair of rollers of a rolling mill which compacts the aluminium powder and electroplated iron to the steel plate, the passage through the said rolling mill producing a reduction in thickness of 5 to 7 percent.
The coated panel is then heated in air at 350C, whereby bonding and sintering occur, after which the coated panel is subjected to a cold reduction to produce a final foil thickness in the range 38 to 60 microns (0.0015 inch to 0.0023 inch). Finally, the product is given a re-crystallization anneal for 24 hours at a temperature in the range of 500 to 550C.
The withdrawal of the panel from the slurry bath may be constituted by vertical withdrawal.
Alternatively, instead of immersing the panel in a slurry bath, the slurry, mentioned above may be applied to the panel by a reverse roller coater as in the conventional paint coating of metal strip.
EXAMPLE IV The procedure is the same as in Example 111 except that the panel, instead of being immersed in a slurry bath, is sprayed with the slurry by the use of compressed air. The slurry employed is thinner i.e. employs more water, than that of Example III, and may for example, be as follows:
Water 280 grams Na O. 2SiO 1.5 grams Ammonium nitrate 1.9 grams Aluminium powder 300 grams Nitric acid Present in an amount to adjust the pH of the slurry to 9.0
Such a slurry may be used to build up a coating of any desired thickness, using known spray painting technology.
EXAMPLE V The procedure is the same as in Example Ill except that the panel instead of being immersed in a slurry bath, is curtain coated, at a speed of up to 240 ft/minute, with a slurry of the following composition:
Water 400 g 'Sodium carboxymethyl cellulose E1000 1 g Sodium dichromate (inhibitor) 0.4 g Aluminium powder (the maximum size of whosepartjcles is in the range of 120 to 400 mesh per linear inch) 600 g (The term F1000 indicates a grade of sodium carboxy methyl cellulose marketed by British Celanese Limited and producing very viscous solutions of low solids content).
The slurry also preferably includes a surfactant such, for example, as an alkyl aryl sulphonate.
If desired, the inhibitor used, instead of being sodium dichromate, could be sodium silicate, sodium chromate, or di-ammonium hydrogen phosphate.
The slurry is made up by first dispersing the water soluble cellulose ether e.g., sodium carboxy methyl cellulose, in the water, and leaving it for an appropriate swelling period. After this the inhibitor is first added, and subsequently the aluminium powder (and the surfactant, if employed).
This particular slurry, after the adjustment of its viscosity by the addition of further water, could also be deposited on the panel by roller coating.
Because of the physical nature of the slurries of Examples III to V, it is not necessary to wet the dried slurries with the sodium carboxy methyl cellulose which is used in Example lto reduce the extent to which the rollers would otherwise dislodge the coating.
We claim:
1. In a method of providing a surface of a steel substrate with an aluminium coating, the said method comprising electroplating the said surface of the steel substrate with a layer of iron, coating the iron layer with a layer containing aluminium powder, and compacting the said iron and powder layers to the substrate, the improvement which consists of subsequently effecting a cold reduction which reduces the gauge of the so-called substrate by at least 30 percent, and effecting a subsequent recrystallisation annealing heat treatment to make the iron and powder layers adhere tightly to the substrate.
2. A method as claimed in claim 1 in which, after compacting the said iron and powder layers and before effecting the cold reduction, the compacted substrate is subjected to an additional heat treatment in the range 300 to 500C.
3. A method as claimed in claim 1 in which the reduction in gauge is in the range of 50 e percent.
4. A method as claimed in claim 1 in which the original substrate has a gauge in the range 0.1 inch to 0.04 inch.
5. A method as claimed in claim 1 in which the recrystallisation anneal is effected at a temperature within the range of 500 to 550C.
6. A method as claimed in claim 1 wherein compaction is effected by passing the coated substrate between a pair of rollers, the substrate, prior to passing between the rollers, being wetted with a liquid which reduces the extent to which the said rollers dislodge the aluminium powder.
7. A method as claimed in claim 1 in which the powder layer is made up of aluminium particles which are applied to the substrate in an electrostatically charged condition, the average particle size of the aluminium particles not exceeding 40 microns.
8. A method as claimed in claim 1 in which the powder layer contains aluminium powder whose average particle size does not exceed 40 microns and also contains a finely divided silicious material which causes the aluminium powder to flow substantially more readily than it would in the absence of the silicious material, the silicious material constituting not more than 0.5 percent by weight of the said powder layer.
9. A method as claimed in claim 8 in which the silicious material comprises particles of silica each of 10 which has been provided with an hydrophobic organic slurry contains a chromate.
* l l l UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION PATENT NO. 3,334,729 DATED y 20, 1975 'NVENTOR(S) 1 Albert Edward Jackson and Ernest Wayne Williams It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
IN 'THE CLAIMS:
Signed and Scaled this twentieth D f January 1976 [SEAL] Arrest:
RUTH C. MASON C. MARSHALL DANN Arresting Officer Commissioner ofParents and Trademarks

Claims (13)

1. IN A METHOD OF PROVIDING A SURFACE OF A STEEL SUBSTRATE WITH AN ALUMINIUM COATING, THE SAID METHOD COMPRISING ELECTROPLATING THE SAID SURFACE OF THE STEEL SUBSTRATE WITH ALAYER OF IRON, COATING THE IRON LAYER WITH A LAYER CONTAINING ALUMINIUM POWDER, AND COMPACTING THE SAID IRON AND POWDER LAYERS TO THE SUBSTRATE, THE IMPROVEMENT WHICH CONSISTS OF SUBSEQUENTLY EFFECTING A COLD REDUCTION WHICH REDUCES THE GAUGE OF THE SO-CALLED SUBSTRATE BY AT LEAST 30 PERCENT, AND EFFECTING A SUBSEQUENT RECRYSTALLISATION ANNEALING HEAT TREATMENT TO MAKE THE IRON AND POWDER LAYERS ADHERE TIGHTLY TO THE SUBSTRATE.
2. A method as claimed in claim 1 in which, after compacting the said iron and powder layers and before effecting the cold reduction, the compacted substrate is subjected to an additional heat treatment in the range 300* to 500*C.
3. A method as claimed in claim 1 in which the reduction in gauge is in the range of 50 - 90 percent.
4. A method as claimed in claim 1 in which the original substrate has a gauge in the range 0.1 inch to 0.04 inch.
5. A method as claimed in claim 1 in which the recrystallisation anneal is effected at a temperature within the range of 500* to 550*C.
6. A method as claimed in claim 1 wherein compaction is effected by passing the coated substrate between a pair of rollers, the substrate, prior to passing between the rollers, being wetted with a liquid which reduces the extent to which the said rollers dislodge the aluminium powder.
7. A method as claimed in claim 1 in which the powder layer is made up of aluminium particles which are applied to the substrate in an electrostatically charged condition, the average particle size of the aluminium particles not exceeding 40 microns.
8. A method as claimed in claim 1 in which the powder layer contains aluminium powder whose average particle size does not exceed 40 microns and also contains a finely divided silicious material which causes the aluminium powder to flow substantially more readily than it would in the absence of the silicious material, the silicious material constituting not more than 0.5 percent by weight of the said powder layer.
9. A method as claimed in claim 8 in which the silicious material comprises particles of silica each of which has been provided with an hydrophobic organic coating.
10. A method as claimed in claim 1 in which the powder layer is applied to the steel substrate in the form of a slurry.
11. A method as claimed in claim 10 in which the slurry contains silica.
12. A method as claimed in claim 10 in which the slurry contains a water soluble cellulose ether.
13. A method as claimed in claim 10 in which the slurry contains a chromate.
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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4045596A (en) * 1975-06-12 1977-08-30 Agence Nationale De Valorisation De La Recherche (Anvar) Superficial treatment of steel
US4061801A (en) * 1975-07-19 1977-12-06 Kawasaki Steel Corporation Method of producing aluminum or aluminum alloy coated steel sheets with aid of powder method
US4121928A (en) * 1975-08-08 1978-10-24 Daido Metal Company Ltd. Method for the manufacture of multi-layer sliding material
US4189522A (en) * 1975-08-08 1980-02-19 Daido Metal Company, Ltd. Multi-layer sliding material and method for manufacturing the same
US4202709A (en) * 1978-03-10 1980-05-13 Furukawa Aluminum Co., Ltd. Method for manufacturing aluminum or aluminum alloy clad steel sheet or strip
US4228203A (en) * 1978-01-27 1980-10-14 Toyo Kogyo Co., Ltd. Method of forming aluminum coating layer on ferrous base alloy workpiece
US4287009A (en) * 1979-11-08 1981-09-01 Bethlehem Steel Corporation Method of producing an aluminum-zinc alloy coated ferrous product to improve corrosion resistance
US4350540A (en) * 1979-11-08 1982-09-21 Bethlehem Steel Corporation Method of producing an aluminum-zinc alloy coated ferrous product to improve corrosion resistance
US4559089A (en) * 1979-10-11 1985-12-17 Texas Instruments Incorporated Method for making a light weight composite of pure aluminum, heat treatable aluminum, and stainless steel
US4567630A (en) * 1981-03-10 1986-02-04 Babcock-Hitachi Kabushiki Kaisha Process of continuously producing plate-shaped catalyst and system therefor
US4602957A (en) * 1984-10-12 1986-07-29 Emi Limited Magnetic powder compacts
US4988479A (en) * 1988-10-06 1991-01-29 Yamaha Corporation Method for producing a composite material
US5904966A (en) * 1993-09-24 1999-05-18 Innovative Sputtering Technology N.V. (I.S.T.) Laminated metal structure
US6534191B2 (en) * 2000-01-28 2003-03-18 Suzuki Motor Corporation Sintered alloy and method for the hardening treatment thereof
US20060079424A1 (en) * 2004-09-23 2006-04-13 Perry Stephen C Buffered acid cleaner and method of production

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3989863A (en) * 1975-07-09 1976-11-02 The International Nickel Company, Inc. Slurry coating process
JPS5340639A (en) * 1976-09-27 1978-04-13 Kawasaki Steel Co Production method of aluminumm or aluminum alloyycoated steel sheet by powder method

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2484118A (en) * 1944-09-22 1949-10-11 Reynolds Metals Co Method of bonding aluminum to steel
US2809891A (en) * 1954-10-12 1957-10-15 Aluminum Co Of America Method of making articles from aluminous metal powder
US2965963A (en) * 1956-09-21 1960-12-27 Jones & Laughlin Steel Corp Aluminum cladding of steel
US3359096A (en) * 1966-05-11 1967-12-19 Texas Instruments Inc Manufacture of coated wire
US3597172A (en) * 1967-01-31 1971-08-03 Deutsche Edelstahlwerke Ag Alloys having an aluminum-diffused surface layer
US3661612A (en) * 1967-12-14 1972-05-09 Summers & Sons Ltd John Method of coating a moving metal strip
US3717513A (en) * 1970-12-23 1973-02-20 Pechiney Process for the production of composite sheets
US3755090A (en) * 1972-03-27 1973-08-28 British Steel Corp A method of providing a surface of a steel substrate with an aluminum coating
US3827140A (en) * 1968-10-17 1974-08-06 Nippon Kokan Kk Method of surface treating steel products with metal powder

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2484118A (en) * 1944-09-22 1949-10-11 Reynolds Metals Co Method of bonding aluminum to steel
US2809891A (en) * 1954-10-12 1957-10-15 Aluminum Co Of America Method of making articles from aluminous metal powder
US2965963A (en) * 1956-09-21 1960-12-27 Jones & Laughlin Steel Corp Aluminum cladding of steel
US3359096A (en) * 1966-05-11 1967-12-19 Texas Instruments Inc Manufacture of coated wire
US3597172A (en) * 1967-01-31 1971-08-03 Deutsche Edelstahlwerke Ag Alloys having an aluminum-diffused surface layer
US3661612A (en) * 1967-12-14 1972-05-09 Summers & Sons Ltd John Method of coating a moving metal strip
US3827140A (en) * 1968-10-17 1974-08-06 Nippon Kokan Kk Method of surface treating steel products with metal powder
US3717513A (en) * 1970-12-23 1973-02-20 Pechiney Process for the production of composite sheets
US3755090A (en) * 1972-03-27 1973-08-28 British Steel Corp A method of providing a surface of a steel substrate with an aluminum coating

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4045596A (en) * 1975-06-12 1977-08-30 Agence Nationale De Valorisation De La Recherche (Anvar) Superficial treatment of steel
US4061801A (en) * 1975-07-19 1977-12-06 Kawasaki Steel Corporation Method of producing aluminum or aluminum alloy coated steel sheets with aid of powder method
US4121928A (en) * 1975-08-08 1978-10-24 Daido Metal Company Ltd. Method for the manufacture of multi-layer sliding material
US4189522A (en) * 1975-08-08 1980-02-19 Daido Metal Company, Ltd. Multi-layer sliding material and method for manufacturing the same
US4228203A (en) * 1978-01-27 1980-10-14 Toyo Kogyo Co., Ltd. Method of forming aluminum coating layer on ferrous base alloy workpiece
US4202709A (en) * 1978-03-10 1980-05-13 Furukawa Aluminum Co., Ltd. Method for manufacturing aluminum or aluminum alloy clad steel sheet or strip
US4559089A (en) * 1979-10-11 1985-12-17 Texas Instruments Incorporated Method for making a light weight composite of pure aluminum, heat treatable aluminum, and stainless steel
US4287009A (en) * 1979-11-08 1981-09-01 Bethlehem Steel Corporation Method of producing an aluminum-zinc alloy coated ferrous product to improve corrosion resistance
US4350540A (en) * 1979-11-08 1982-09-21 Bethlehem Steel Corporation Method of producing an aluminum-zinc alloy coated ferrous product to improve corrosion resistance
US4567630A (en) * 1981-03-10 1986-02-04 Babcock-Hitachi Kabushiki Kaisha Process of continuously producing plate-shaped catalyst and system therefor
US4602957A (en) * 1984-10-12 1986-07-29 Emi Limited Magnetic powder compacts
US4988479A (en) * 1988-10-06 1991-01-29 Yamaha Corporation Method for producing a composite material
US5904966A (en) * 1993-09-24 1999-05-18 Innovative Sputtering Technology N.V. (I.S.T.) Laminated metal structure
US6534191B2 (en) * 2000-01-28 2003-03-18 Suzuki Motor Corporation Sintered alloy and method for the hardening treatment thereof
US20060079424A1 (en) * 2004-09-23 2006-04-13 Perry Stephen C Buffered acid cleaner and method of production

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BE806866A (en) 1974-02-15
AU6200773A (en) 1975-05-01
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GB1397258A (en) 1975-06-11
DE2355001A1 (en) 1974-05-16

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