Classifications

• • 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
  • C23C10/00—Solid state diffusion of only metal elements or silicon into metallic material surfaces
  • C23C10/28—Solid state diffusion of only metal elements or silicon into metallic material surfaces using solids, e.g. powders, pastes
  • C23C10/34—Embedding in a powder mixture, i.e. pack cementation
• • Y—GENERAL 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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T29/00—Metal working
  • Y10T29/49—Method of mechanical manufacture
  • Y10T29/4998—Combined manufacture including applying or shaping of fluent material
  • Y10T29/49982—Coating
• • Y—GENERAL 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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/12—All metal or with adjacent metals
  • Y10T428/12014—All metal or with adjacent metals having metal particles
  • Y10T428/12028—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, etc.]
  • Y10T428/12063—Nonparticulate metal component
  • Y10T428/12139—Nonmetal particles in particulate component
• • Y—GENERAL 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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/12—All metal or with adjacent metals
  • Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
  • Y10T428/12771—Transition metal-base component
  • Y10T428/12861—Group VIII or IB metal-base component
  • Y10T428/12951—Fe-base component
  • Y10T428/12958—Next to Fe-base component
  • Y10T428/12965—Both 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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• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Mechanical Engineering (AREA)
• Metallurgy (AREA)
• Organic Chemistry (AREA)
• Other Surface Treatments For Metallic Materials (AREA)
• Chemical Treatment Of Metals (AREA)

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Citations (9)

• 1972
  • 1972-11-03 GB GB5077372A patent/GB1397258A/en not_active Expired
• 1973
  • 1973-10-25 CA CA184,253A patent/CA996846A/en not_active Expired
  • 1973-10-30 IT IT7330734A patent/IT1003159B/it active
  • 1973-10-31 BE BE137373A patent/BE806866A/xx unknown
  • 1973-11-01 US US411846A patent/US3884729A/en not_active Expired - Lifetime
  • 1973-11-01 JP JP48122264A patent/JPS4995829A/ja active Pending
  • 1973-11-02 NL NL7315096A patent/NL7315096A/xx not_active Application Discontinuation
  • 1973-11-02 DE DE19732355001 patent/DE2355001A1/de not_active Withdrawn
  • 1973-11-02 FR FR7339124A patent/FR2205587B1/fr not_active Expired

Patent Citations (9)

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