EP2845929B1 - Tinplate with a polymer coating and method for producing the same - Google Patents

Tinplate with a polymer coating and method for producing the same Download PDF

Info

Publication number
EP2845929B1
EP2845929B1 EP14171749.6A EP14171749A EP2845929B1 EP 2845929 B1 EP2845929 B1 EP 2845929B1 EP 14171749 A EP14171749 A EP 14171749A EP 2845929 B1 EP2845929 B1 EP 2845929B1
Authority
EP
European Patent Office
Prior art keywords
tin
coating
polymer
tinplate
polymer coating
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP14171749.6A
Other languages
German (de)
French (fr)
Other versions
EP2845929A1 (en
Inventor
Kathleen Dr. Stein-Fechner
Tanja Dr. Lommel
Reiner Dr. Sauer
Beate Dr. Bannemann
Petra Diederich
Benjamin Liebscher
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ThyssenKrupp Rasselstein GmbH
Original Assignee
ThyssenKrupp Rasselstein GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=50884806&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP2845929(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by ThyssenKrupp Rasselstein GmbH filed Critical ThyssenKrupp Rasselstein GmbH
Priority to RS20171217A priority Critical patent/RS56605B1/en
Priority to PL14171749T priority patent/PL2845929T3/en
Publication of EP2845929A1 publication Critical patent/EP2845929A1/en
Application granted granted Critical
Publication of EP2845929B1 publication Critical patent/EP2845929B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • 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
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/34Pretreatment of metallic surfaces to be electroplated
    • C25D5/36Pretreatment of metallic surfaces to be electroplated of iron or steel
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D25/00Details of other kinds or types of rigid or semi-rigid containers
    • B65D25/14Linings or internal coatings
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D25/00Details of other kinds or types of rigid or semi-rigid containers
    • B65D25/34Coverings or external coatings
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/005Apparatus specially adapted for electrolytic conversion coating
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/02Anodisation
    • C25D11/34Anodisation of metals or alloys not provided for in groups C25D11/04 - C25D11/32
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/48After-treatment of electroplated surfaces
    • C25D5/50After-treatment of electroplated surfaces by heat-treatment
    • C25D5/505After-treatment of electroplated surfaces by heat-treatment of electroplated tin coatings, e.g. by melting
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D7/00Electroplating characterised by the article coated
    • C25D7/06Wires; Strips; Foils
    • C25D7/0614Strips or foils
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D7/00Electroplating characterised by the article coated
    • C25D7/06Wires; Strips; Foils
    • C25D7/0614Strips or foils
    • C25D7/0621In horizontal cells
    • 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.]
    • Y10T428/12535Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.] with additional, spatially distinct nonmetal component
    • Y10T428/12542More than one such component
    • Y10T428/12549Adjacent to each other

Definitions

  • the invention relates to a coated with a polymer coating tinplate and method for its preparation and an apparatus for performing the method.
  • Tinplate is a thin, cold-rolled steel sheet, the surface of which is coated with tin.
  • the application of the tin coating on the steel sheet is usually carried out electrolytically.
  • Tinplate is mainly used for the production of packaging, in particular cans for food and pet food, packaging for chemical and technical products, aerosol cans, beverage cans and for the production of parts for such packaging as e.g. Closures, flap bands, valve plates, can ends and lid rings used.
  • Tinplate is characterized by high corrosion resistance and stability against acids as well as good formability.
  • the tinplate surface is additionally provided with a paint coating, in addition to the corrosion protection provided by the tin coating to provide additional protection against corrosion.
  • WO 2013/104530 A2 discloses a method for passivation of tinplate, in which a tin-plated steel strip with a belt speed of at least 200 m / min is moved through a coating plant, wherein after the tinning of the steel strip, the surface is anodized and applied to the oxide layer, a liquid solution of a chromium-free aftertreatment agent becomes.
  • an oxide layer consisting essentially of tetravalent tin oxide (SnO 2 ) is formed between the tin layer and the surface layer of the post-treatment agent.
  • a lacquer layer can be applied to the surface layer of the aftertreatment agent, for which purpose the aftertreatment agent is selected such that a good lacquer adhesion and wetting of the surface layer with conventional lacquer materials can be ensured.
  • the post-published WO 2014/006031 A1 discloses a method for passivating a tinplate surface by forming a tin oxide layer on the tin surface, wherein the tinplate is oxidized in an anodic treatment in an aqueous electrolyte and then subjected to a passivating treatment with a hexavalent chromium-free passivating agent.
  • the passivated tinplate can then be provided with an organic coating which consists of an (epoxy-phenolic) gold lacquer, white lacquer (epoxy anhydride lacquer) or polyester lacquer, a PVC or a vinyl-organosol coating or a water-dilutable epoxy-amino or Epoxy-acrylic-amino coating material may consist. Due to the good adhesion of these coating materials to the passivated tin surface, the product can be used as a replacement for CDC (cathodic dichromate) treated and subsequently coated with a polymeric material.
  • CDC cathodic dichromate
  • Tinplate can also be provided with polymer coatings to prevent corrosion of the steel, for example by applying a plastic film of polyethylene terephthalate (PET) or polypropylene (PP).
  • PET polyethylene terephthalate
  • PP polypropylene
  • Such sheet-coated tinplate is particularly suitable for the production of valve plates, floors of aerosol cans, tear-open lid for cans and deep-drawn containers and vacuum closures.
  • Tinned steel sheets are known, which are coated with a polyester resin film, in particular of polyethylene terephthalate (PET).
  • PET polyethylene terephthalate
  • the coating of the tinplate surface With the polyester resin film is carried out by laminating a polyester film, in particular a PET film, on the surface of the tinplate.
  • a chromium-containing adhesive layer is applied to the tinplate surface prior to laminating the polyester resin film, formed for example by a monolayer of hydrated chromium oxide or by a double layer of metallic chromium with an overlying layer of hydrated chromium oxide ,
  • the polyester resin film especially a PET film, would peel off the tinplate, particularly in forming processes in the packaging manufacturing processes or in sterilizing or filling the packages with hot fillers.
  • the chromium compounds used for the preparation of the chromium-containing adhesive layer are toxic and environmentally hazardous.
  • electrolytic chromium coated steel As an alternative material for tinplate, electrolytic chromium coated steel (ECCS) is known from the prior art.
  • This material also known as "Tin-Free Steel (TFS)"
  • TFS Tin-Free Steel
  • the surface of this material has good adhesion to polymeric materials, e.g. for polyethylene terephthalate or polypropylene, and therefore can be coated with these polymers, for example by laminating a polymeric film to allow additional corrosion protection.
  • the adhesion of the polymer coating on the chromium surface of the ECCS or TFS also holds strong transformations, such as occur in the production of packaging containers, as well as sterilization processes stood.
  • Polymer coated ECCS sheets are therefore particularly used in manufacturing processes for containers in which severe deformation of the sheets is required, e.g. in the manufacture of valve plates for aerosol cans, wherein the organic coating in the ECCS before forming takes place, otherwise severe tool wear occurs.
  • a corrosion-resistant steel sheet which has a metallic corrosion protection layer, which may be, for example, electrolytically applied tin or chromium / chromium oxide layers on which one or both sides a transparent polymer film is applied by laminating a polymer film.
  • the polymer film consists of polyethylene terephthalate (PET), polyvinyl chloride (PVC) or polypropylene (PP).
  • an adhesion promoter in particular an adhesive layer, is provided between the metallic corrosion protection layer of the steel sheet and the laminated polymer film.
  • a galvanically coated with a metallic corrosion protection layer and passivated steel sheet with a thickness between 0.05 mm and 0.5 mm is used and heated to temperatures of about 160 ° C.
  • the polymer film is laminated by means of rotating rollers.
  • the thickness of the laminated polymer film is between 5 and 100 microns.
  • the polymer film preferably has on one side an adhesive layer which has a lower melting point than the polymer material of the polymer film.
  • the polymer film is laminated with the adhesive layer on the surface of the metallic corrosion protection layer of the steel sheet oriented.
  • a special polymer film having an adhesive layer is used to laminate the polymer film on the surface of the anticorrosion layer of the steel sheet.
  • Such polymer films with an adhesive layer are very expensive to manufacture.
  • the handling of such polymer films with an adhesive layer is more complicated and the process parameters, in particular the temperatures, must be kept during the lamination within the predetermined limits, which are determined by the melting temperatures of the polymer film and the adhesive layer.
  • an adhesive layer can not be dispensed with if sufficiently good adhesion of the polymer film to the tinned surface of the steel sheet is to be ensured.
  • the polymer films adhere better, but fall in the production of ECCS, because of the chromium-containing substances used in the coating of the steel sheet, toxic and polluting waste.
  • the object of the invention is to provide a method which is as completely as possible free of chromium for the production of a highly corrosion-resistant steel sheet.
  • the highly corrosion-resistant steel sheet produced by the method should be suitable in particular for the production of packaging and suffer no deterioration in terms of corrosion resistance even with severe deformations in the manufacturing process and sterilization of the package produced.
  • the chromium-free tin surface of the tinned steel sheet is first electrochemically oxidized in a first step and in a second step a polymer coating is applied to the oxidized tin surface.
  • the electrochemical oxidation of the tin surface ensures chromium-free passivation of the tin surface, which prevents unhindered growth of tin oxide on the tinplate surface.
  • the passivation of the tinplate surface takes place in the process according to the invention without the use of chromium-containing substances, in particular without the use of toxic and environmentally hazardous chromium oxides. It has surprisingly been found that this chromium-free passivation of the tinplate surface by electrochemical oxidation not only prevents unhindered growth of tin oxide on the tinplate surface, but at the same time also forms a good adhesion base for polymers.
  • a polymer coating can easily be oxidized onto the Tin surface of the tinplate are applied, the oxidized tin surface allows a very good adhesion of the polymer coating. It has been found that the adhesion between the oxidized tin surface and the polymer coating also withstands severe deformation, as occurs, for example, in processes for the production of multi-deep-drawn cans or in the manufacture of valve plates. The adhesion between the oxidized tin surface and the polymer coating also readily withstands sterilization, without any detachment of the polymer coating from the tinplate surface during sterilization.
  • a tin coating is deposited electrolytically on one or both sides of a steel sheet.
  • an electrochemical oxidation of the surface of the tin coating takes place and finally a polymer coating is applied to the oxidized surface of the tin coating.
  • the electrochemical oxidation of the tin surface is preferably carried out directly and in particular within a few seconds after the deposition of the tin coating on the steel sheet.
  • the electrochemical oxidation of the tin surface preferably takes place here without further intermediate steps, in particular without intermediate cleaning or temperature treatment of the tinplate surface.
  • the electrochemical oxidation of the tin surface can be carried out in particular by anodic polarization of the tinned steel sheet in an aqueous and chromium-free electrolyte.
  • the electrochemical oxidation of the tin surface may be carried out by immersing the tinplate in a soda solution (sodium carbonate solution).
  • a thin tin oxide layer which consists essentially of tetravalent tin oxide (SnO 2 ), forms on the (chromium-free) tin surface of the tinplate.
  • This tetravalent tin oxide is significantly more inert than divalent tin oxide (SnO), which is formed on the tinplate surface when tinplate is stored in an oxygen-containing atmosphere, and prevents unhindered growth of a (divalent) tin oxide layer on the tinplate surface upon contact with oxygen.
  • the thickness of the oxide layer of essentially tetravalent tin oxide formed during the electrochemical oxidation of the tinplate surface is expediently in the nm range and is preferably thinner than 100 nm.
  • this passivating tin oxide layer on the Tinplate surface is preferably generated in the step of electrochemical oxidation, a charge density on the tin surface, which is at most 40 C / m 2 .
  • the polymer coating expediently has a thickness in the range of 10 to 100 microns and is preferably applied by laminating a polymer film on the oxidized tin surface.
  • the adhesion promoter layer further increases the inherently good adhesion of the polymer coating to the oxidized tin surface of the tinplate.
  • the tinned steel sheet is heated to temperatures above the melting temperature of the tin coating (232 ° C.) during the lamination of the polymer film.
  • the tin coating of the tinplate is melted, so that at least the near-surface areas of the tin coating of the tinplate are in the molten state during the lamination of the polymer film. This further improves the adhesion between the (molten) tin surface of the steel sheet and the laminated polymer coating.
  • the polymer material of the polymer coating is expediently a thermoplastic polyester, in particular polyethylene terephthalate (PET).
  • PET polyethylene terephthalate
  • the melting point of polyethylene terephthalate is in the range of 260-270 ° C.
  • a multilayer plastic film for forming the polymer coating which has an antiblocking layer on its upper side.
  • an antiblocking layer may be formed, for example, by a silicon oxide layer on top of the polymer film.
  • the processes according to the invention can be carried out in strip-tinning plants in which a steel strip is moved by means of a transport device at a strip speed of preferably more than 200 m / min and more preferably of more than 500 m / min through a tinning device, around one or both sides of the steel strip electrolytically coated with a tin coating.
  • the subsequent electrochemical oxidation of the tin surface is carried out in an oxidation device preferably by passing the tinned steel strip at the belt speed through an electrolytic bath with an aqueous electrolyte, wherein the steel strip is suitably connected as an anode to electrochemically (anodically) oxidize the tin surface.
  • the polymer coating is applied to the oxidized tin surface of the running steel strip in a plastic coating device, for which purpose preferably by means of laminating rollers on one or both sides a polymer film is laminated onto the oxidized tin surface.
  • the tinning device and the oxidation device are arranged one behind the other in the belt running direction and preferably so close to each other that at the typical belt speeds of more than 200 m / min within a very short time and preferably within a few seconds after the tin coating, the tinned surface of the steel belt can be electrochemically oxidized ,
  • the starting material for the process according to the invention for the production of a polymer coating coated tinplate is preferably a hot rolled and unalloyed or low-alloyed sheet steel (steel strip) with a low carbon content of, for example, 20 to 900 ppm.
  • the alloy components of the steel suitably meet the requirements of the international standard ASTM A 623-11 (Standard Specification for Tin Mill Products), whereby a use of the tinplates according to the invention produced for the production of food packaging is ensured.
  • ASTM A 623-11 Standard Specification for Tin Mill Products
  • the hot-rolled steel strip is first pickled in a (not shown) pickling plant, then rinsed and dried and then cold-rolled in a cold rolling mill.
  • the steel strip is rolled to a thickness of less than 1.0 mm (thin sheet) and preferably to thicknesses of 0.1 to 0.5 mm (fine sheet).
  • the steel strip is first passed through a continuous annealing furnace in which the steel strip is heated to temperatures of 550 ° C to 700 ° C to recrystallize the steel to anneal.
  • the recrystallizing annealing reestablishes the formability of the cold rolled steel strip.
  • the steel strip may be dressed or regrooved in a post-rolling mill if necessary to achieve the forming properties necessary for the intended processing purposes. When re-rolling, if necessary, a required further reduction in the thickness of the steel strip can be achieved. After the temper rolling or rolling, the steel strip is cleaned by an alkaline electrolytic treatment and by pickling with subsequent rinsing.
  • the steel strip 10 as in FIG. 1 shown schematically, guided by a tinning 7.
  • the steel strip 10 is unwound as a continuous belt from a roll 12 and moved by a conveyor 6 at a belt speed of preferably more than 200 m / min and up to 750 m / min through a tank 7a with a tin-containing electrolyte and carried out as a cathode between tin anodes ,
  • the tin of the anodes is dissolved and deposited on the steel strip as a tin coating.
  • the tin can be deposited in any thickness and, if necessary, on both sides of the steel strip 10.
  • the thickness of the applied tin layer is regularly between 0.5 g / m 2 and 12 g / m 2 . However, it is also possible to coat the steel strip with thinner or thicker tin layers.
  • the tin surface of the tin-plated steel strip 10 is electrochemically oxidized in an oxidizer 8.
  • the freshly tinned steel strip 10 is, for example, passed into an electrolysis bath with an acidic, chromium-free and aqueous electrolyte and connected as an anode.
  • the fresh tin surface of the tinned steel strip 10 is anodically polarized.
  • a tin oxide layer having a layer thickness in the nm range is formed on the tin surface of the tin-plated steel strip, which consists essentially of tetravalent tin oxide (SnO 2 ).
  • This tetravalent tin oxide is much more inert to divalent tin oxide (SnO) that forms when tinned steel sheet is stored in an oxygen atmosphere.
  • This (essentially tetravalent and inert) tin oxide layer which forms during the electrochemical oxidation of the freshly tinned surface, ensures high resistance of the tinned steel strip surface against corrosion and reaction with sulfur.
  • the thin tin oxide layer of essentially tetravalent tin oxide (SnO 2 ) prevents, in particular, unimpeded growth of further (bivalent) tin oxide upon contact of the tinned surface with atmospheric oxygen.
  • the electrochemical oxidation of the tin surface takes place, for example, as anodic oxidation of the tinned steel strip 10 in soda solution, i. in an aqueous sodium carbonate solution.
  • the tin-plated steel strip is moved further at the strip speed and passed through an electrolytic bath 8a with a soda solution.
  • the concentration of sodium carbonate in the soda solution is preferably 1 wt .-% to 10 wt .-%, preferably 2 wt .-% to 8 wt .-%, preferably 3 wt .-% to 7 wt .-%, especially 4 Wt .-% to 6 wt .-%, in particular about 5 wt .-%.
  • the oxidation device 8 for the electrochemical oxidation of the surface of the tin coating expediently comprises an electrolytic bath 8a with a vertical tank which is filled with the electrolyte. In the vicinity of the bottom, a deflection roller is disposed within the vertical tank, via which the tinned steel strip 10 is deflected. Between the tinned steel strip 10 and the counter electrode (eg, a steel cathode) in the vertical tank, a potential is applied.
  • the amount of charge Q transferred during the electrochemical oxidation is preferably below 40 C / m 2 .
  • the current density prevailing in the electrolysis bath is preferably in the range from 1.0 A / dm 2 to 3 A / dm 2 .
  • the thickness of the thereby forming tin oxide layer is preferably less than 100 nm and is particularly preferably of the order of 10 nm.
  • the anodization time corresponds to the residence time of the tinned steel strip in the electrochemical oxidation bath (electrolyte bath). This is predetermined by the length of the electrolyte bath or its fill level as well as the anode length and the belt speed and is advantageously in the range of 0.1 s to 1 s, in particular between 0.1 s and 0.7 s, preferably in the typical belt speeds Range from 0.15s to 0.5s, and ideally 0.2s.
  • the fill level can be used to set the anodization time to suitable values, depending on the belt speed, in order to form the preferred layer thickness of the electrochemically produced tin oxide layer.
  • the distance between the steel strip 10 and the counter electrode in the electrolytic 8a is set due to the system. It is, for example, in the range of 3 to 15 cm, preferably in the range of 5 to 10 cm and in particular by 10 cm.
  • the temperature of the electrolyte is preferably in the range of 30 to 60 ° C, in particular in the range of 35 to 50 ° C.
  • the current density in the electrolysis bath is set, for example, in the range from 1.0 to 3 A / dm 2 , preferably 1.3 to 2.8 A / dm 2 , and in particular by 2.4 A / dm 2 .
  • the total amount of charge moves in the range between 0.2 C and 0.4 C and is preferably, for example, 0.3 C.
  • the corresponding charge densities are in the range of 0.2 C / dm 2 to 0.4 C / dm 2 .
  • the tin-plated steel strip 10 is guided into a plastic coating device 9 after the electrochemical oxidation of the tin surface at a maximum strip speed of 200 m / min. Since the steel strip can not be performed by the plastic coating device with the high belt speeds of about 750 m / min, which are driven in tinning the steel strip in the tinning, it is appropriate to the process step of the polymer coating separately, ie with preceding rolling of the tinned steel strip to perform a coil and intermediate storage of the coil. This is easily possible since the tin surface is resistant to a (further) unhindered growth of a (divalent) tin oxide layer due to the electrochemical oxidation.
  • the polymer coating without intermediate storage and istdem Apply steel strip directly after tinning and oxidizing the tin surface in the plastic coating device 9.
  • a polymer coating is applied to one or both sides of the tinned steel strip.
  • the steel strip is first heated in a heater 11, which may be formed, for example.
  • a heater 11 which may be formed, for example.
  • induction heating or as infrared or microwave heating to temperatures which are at least above the melting temperature of the tin (232 ° C).
  • the temperature of the steel strip 10 during application of the polymer coating is also above the melting temperature of the polymer material.
  • the polymer material is preferably polyethylene terephthalate (PET having a melting point of approx.
  • the heated steel strip 10 is supplied in the plastic coating device 9 on one or both sides of a film 16 made of a polymer material and pressed by (suitably heated) laminating rollers 9a to the surface of the tin coating.
  • the polymer film 16 may be a film of a polyester such as polyethylene terephthalate and in particular a biaxially oriented or amorphous polyester film or a film of polypropylene or else a film of a polymer laminate consisting of polyethylene terephthalate and polypropylene and polyethylene. If necessary, a polymer film having a primer layer is used, which will be described later.
  • a multilayer polymer film 16 for forming the polymer coating which has an antiblocking layer on its upper side.
  • an antiblocking layer may be formed, for example, by a silicon oxide layer on top of the polymer film.
  • the tin and polymer coated steel strip 10 undergoes cooling to about 20 ° C. Thereafter, the polymer coating can optionally be completely melted and then quenched in a cooling device 15 (for example a water bath) to a temperature below the glass transition point.
  • a cooling device 15 for example a water bath
  • an amorphous structure is formed in the polyethylene terephthalate or a minimal crystalline structure in the polypropylene.
  • the melting of the polymer coating is carried out particularly expediently by re-heating the steel strip 10 to temperatures above the melting point of the polymer material used in a melting device 14.
  • the plastic coating of the polymer coating takes place expediently in the melting device 14 by induction heating of the steel strip 10 in an induction coil 14a.
  • This reheating residual stresses in the polymer coating are broken down by relaxation, which leads to an increase in the adhesion between the tin coating and the polymer coating and, as a result, to a stabilization of the composite of these layers.
  • the relaxation time is less than 0.5 seconds, so that a brief heating of the polymer coating to temperatures above the PET melt temperature (about 260 ° C) is sufficient to provide the desired relaxation.
  • an induction coil 14a extends in the melting device 14 for less than 1 meter along the strip running direction, in order to heat the steel strip 10 inductively in this section, and thus the Melt polymer coating.
  • the subsequent quenching of the molten polymer coating in the cooling device 15 can, for example. By air cooling or by immersing the Steel bands into a tank with coolant. Finally, the coated steel strip 10 is wound on a roller 13 by the transport device 6.
  • FIG. 2 a correspondingly manufactured tinplate is shown in section. This comprises the layers of steel sheet 1, tin coating 2, tin oxide layer 3 and the polymer coating 4 (for example of PET).
  • the tinplates produced according to the invention are distinguished by high corrosion resistance, which is achieved by the metallic corrosion protection layer made of tin and the polymer coating.
  • the thin iron-tin alloy layer which is formed when the tin-plated steel strip is heated to temperatures above the tin melting point between the steel strip surface and the tin layer, also contributes to the corrosion resistance.
  • the combination of these anticorrosive layers is particularly advantageous because the release of tin ions from the tin coating is avoided when exposed to air by the polymer coating. Because of the polymer coating, the tinplates produced according to the invention are also inert towards aggressive and, in particular, acidic filling products and are therefore very well suited for the production of packaging for such filling products.
  • the tinplates according to the invention have a high brilliance due to the glossy surface of the tin coating, which results from a complete melting of the tin coating. This is particularly advantageous when using transparent or translucent polymer coatings, because the tinplate thereby has an optically very attractive glossy surface.
  • the processes according to the invention are further characterized in that they are completely free of chromium, i. no chromium-containing substances are used.
  • the steel strips produced according to the invention are further distinguished by a very good adhesion of the polymer coating to the tin coating, which is already achieved without adhesion promoters or additional adhesive layers due to the oxidized tin surface.
  • the additional use of primer layers between the tin coating and the polymer coating is only required for special applications where very high forming rates occur.
  • Suitable adhesion promoters are glycol modified polyethylene terephthalate (PETG wherein less than 50% of the diol component is cyclohexadimethanol), glycol modified polycyclohexylenedimethylene terephthalate (PCTG wherein more than 50% of the diol component is cyclohexadimethanol) and / or isophthalic acid (IPA). Coupling agents which have a proportion of PETG and 5 to 25% by volume of IPA or PCTG have proven to be particularly preferred.
  • PETG glycol modified polyethylene terephthalate
  • PCTG glycol modified polycyclohexylenedimethylene terephthalate
  • IPA isophthalic acid
  • a multilayered polymer film which contains a polymer layer (for example of PET) and an adhesion promoter layer of one of the abovementioned materials.
  • a polymer layer for example of PET
  • an adhesion promoter layer of one of the abovementioned materials.
  • Such polymer films are available as coextruded films, wherein the thickness of the adhesion promoter layer in the range of 3 to 6 microns with a total thickness of the polymer film from 10 to 40 microns.
  • This multilayered polymer film is oriented toward the tin surface for application of the polymer coating with the adhesion promoter layer and is thus laminated onto the oxidized tin surface.
  • a correspondingly manufactured tinplate is shown in section. This comprises the layers of steel sheet 1, tin coating 2, tin oxide layer 3 and the laminated polymer coating with the adhesion promoter layer 5 and the polymer layer 4 (for example made of PET).
  • the tinplates produced according to the invention are suitable for the production of packaging containers, in particular for foodstuffs and for technical filling goods, such as, for example, two-part cans (deep-drawn and stretched, DWI cans) and aerosol cans.
  • Canned hulls of three-piece cans are also suitable if, before the hull welding Polymer coating is removed in the welding area.
  • parts of such packaging containers from the steel strips produced according to the invention, such as flap bands, valve plates, can covers and cover rings.
  • the inventive method can also be used for the production of steel sheets for use in other areas, such as for the production of sheets for the construction sector or for the production of household appliances.
  • the invention is not limited to the described embodiments.
  • a roll coil
  • application of the polymer coating This is in the schematic representation of the device according to the invention FIG. 1 not considered.
  • the polymer coating may also be applied to the tin coating by other than laminating methods.
  • a molten polymer material can be applied to the oxidized tin coating, as for example in the Patent DE 197 30 893 C1 is described.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Electrochemistry (AREA)
  • Mechanical Engineering (AREA)
  • Laminated Bodies (AREA)
  • Electroplating Methods And Accessories (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)
  • Containers Having Bodies Formed In One Piece (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Description

Die Erfindung betrifft ein mit einer Polymerbeschichtung beschichtetes Weißblech sowie Verfahren zu dessen Herstellung und eine Vorrichtung zur Durchführung der Verfahren.The invention relates to a coated with a polymer coating tinplate and method for its preparation and an apparatus for performing the method.

Weißblech ist ein dünnes, kaltgewalztes Stahlblech, dessen Oberfläche mit Zinn beschichtet ist. Das Aufbringen der Zinnbeschichtung auf dem Stahlblech erfolgt in der Regel elektrolytisch. Weißblech wird hauptsächlich zur Herstellung von Verpackungen, insbesondere von Dosen für Lebensmittel und Tiernahrung, Verpackungen für chemisch-technische Füllgüter, Aerosoldosen, Getränkedosen und für die Herstellung von Teilen für solche Verpackungen wie z.B. Verschlüsse, Laschenbänder, Ventilteller, Dosendeckel und Deckelringe verwendet.Tinplate is a thin, cold-rolled steel sheet, the surface of which is coated with tin. The application of the tin coating on the steel sheet is usually carried out electrolytically. Tinplate is mainly used for the production of packaging, in particular cans for food and pet food, packaging for chemical and technical products, aerosol cans, beverage cans and for the production of parts for such packaging as e.g. Closures, flap bands, valve plates, can ends and lid rings used.

Weißblech zeichnet sich durch eine hohe Korrosionsbeständigkeit und Stabilität gegen Säuren sowie durch eine gute Umformbarkeit aus. Für bestimmte Anwendungen, beispielsweise zur Herstellung von Lebensmittelverpackungen und Getränkedosen, wird die Weißblechoberfläche zusätzlich mit einer Lackbeschichtung versehen, um neben dem Korrosionsschutz durch die Zinnbeschichtung einen zusätzlichen Schutz vor Korrosion zu gewährleisten.Tinplate is characterized by high corrosion resistance and stability against acids as well as good formability. For certain applications, for example for the production of food packaging and beverage cans, the tinplate surface is additionally provided with a paint coating, in addition to the corrosion protection provided by the tin coating to provide additional protection against corrosion.

Aus der WO 2013/104530 A2 ist ein Verfahren zur Passivierung von Weißblech bekannt, in dem ein verzinntes Stahlband mit einer Bandgeschwindigkeit von wenigstens 200 m/min durch eine Beschichtungsanlage bewegt wird, wobei nach dem Verzinnen des Stahlbandes die Oberfläche anodisch oxidiert und auf die Oxidschicht eine flüssige Lösung eines chromfreien Nachbehandlungsmittels aufgetragen wird. Dadurch entsteht zwischen der Zinnschicht und der Oberflächenschicht des Nachbehandlungsmittels eine Oxidschicht, welche im Wesentlichen aus vierwertigem Zinnoxid (SnO2) besteht. Auf die Oberflächenschicht des Nachbehandlungsmittels kann eine Lackschicht aufgebracht werden, wofür das Nachbehandlungsmittel so ausgewählt wird, dass eine gute Lackhaftung und Benetzung der Oberflächenschicht mit üblichen Lackmaterialien gewährleistet werden kann.From the WO 2013/104530 A2 discloses a method for passivation of tinplate, in which a tin-plated steel strip with a belt speed of at least 200 m / min is moved through a coating plant, wherein after the tinning of the steel strip, the surface is anodized and applied to the oxide layer, a liquid solution of a chromium-free aftertreatment agent becomes. As a result, an oxide layer consisting essentially of tetravalent tin oxide (SnO 2 ) is formed between the tin layer and the surface layer of the post-treatment agent. A lacquer layer can be applied to the surface layer of the aftertreatment agent, for which purpose the aftertreatment agent is selected such that a good lacquer adhesion and wetting of the surface layer with conventional lacquer materials can be ensured.

Die nachveröffentlichte WO 2014/006031 A1 offenbart ein Verfahren zur Passivierung einer Weißblechoberfläche durch Ausbildung einer Zinnoxidschicht auf der Zinnoberfläche, wobei das Weißblech in einer anodischen Behandlung in einem wässrigen Elektrolyten oxidiert und anschließend einer Passivierungsbehandlung mit einem von hexavalentem Chrom freien Passivierungsmittel unterzogen wird. Das passivierte Weißblech kann anschließend mit einer organischen Beschichtung versehen werden, welche aus einem (epoxy-phenolischen) Goldlack, Weißlack (Epoxy-Anhydrid-Lack) oder Polysterlack, einer PVC- oder einer Vinyl-Organosol-Beschichtung oder einem wasserverdünnbaren Epoxy-Amino oder Epoxy-Acryl-Amino-Beschichtungsmaterial bestehen kann. Aufgrund einer guten Haftung dieser Beschichtungsmaterialien auf der passivierten Zinnoberfläche kann das Produkt als Ersatz für mit CDC (cathodic dichromate) behandelten und anschließend mit einem Polymermaterial beschichteten Blechen eingesetzt werden.The post-published WO 2014/006031 A1 discloses a method for passivating a tinplate surface by forming a tin oxide layer on the tin surface, wherein the tinplate is oxidized in an anodic treatment in an aqueous electrolyte and then subjected to a passivating treatment with a hexavalent chromium-free passivating agent. The passivated tinplate can then be provided with an organic coating which consists of an (epoxy-phenolic) gold lacquer, white lacquer (epoxy anhydride lacquer) or polyester lacquer, a PVC or a vinyl-organosol coating or a water-dilutable epoxy-amino or Epoxy-acrylic-amino coating material may consist. Due to the good adhesion of these coating materials to the passivated tin surface, the product can be used as a replacement for CDC (cathodic dichromate) treated and subsequently coated with a polymeric material.

Weißblech kann zur Vermeidung der Korrosion des Stahls auch mit Polymerbeschichtungen versehen werden, bspw. durch Aufbringen einer Kunststofffolie aus Polyethylenterephthalat (PET) oder Polypropylen (PP). Derart folienbeschichtetes Weißblech ist insbesondere für die Herstellung von Ventiltellern, Böden von Aerosoldosen, Aufreißdeckel für Dosen sowie tiefgezogene Behälter und Vakuumverschlüsse geeignet.Tinplate can also be provided with polymer coatings to prevent corrosion of the steel, for example by applying a plastic film of polyethylene terephthalate (PET) or polypropylene (PP). Such sheet-coated tinplate is particularly suitable for the production of valve plates, floors of aerosol cans, tear-open lid for cans and deep-drawn containers and vacuum closures.

Es hat sich allerdings gezeigt, dass beim Umformen von mit PET-Beschichtungen versehenen Weißblechen Spannungsrisse in der PET-Beschichtung entstehen, welche bei Kontakt mit aggressiven und insbesondere säurehaltigen Füllgütern dazu führen, dass die darunter liegende Zinnbeschichtung des Weißblechs angegriffen wird. Auch die Emulsionen von Schmiermitteln, die zur besseren Verarbeitbarkeit auf die Weißblechoberfläche aufgetragen werden, sind für die Rissinitiierung im PET mitverantwortlich und können darüber hinaus in die gebildeten Risse in der PET-Beschichtung eintreten und die Zinnoberfläche des Weißblechs angreifen, was zu einem Haftungsverlust und zu einer Ablösung der PET-Beschichtung von der Weißblechoberfläche führen kann.However, it has been shown that during the forming of tinplates provided with PET coatings, stress cracks develop in the PET coating, which, when in contact with aggressive and in particular acidic contents, causes the underlying tin coating of the tinplate to be attacked. The emulsions of lubricants which are applied to the tinplate surface for better processability are also responsible for crack initiation in the PET and, moreover, can penetrate into the formed cracks in the PET coating and attack the tin surface of the tinplate, leading to loss of adhesion and to a detachment of the PET coating can lead from the tinplate surface.

Aus den Veröffentlichungen DE 40 09 839 A1 , DE 34 36 412 C2 und EP 664 209 A1 sind verzinnte Stahlbleche bekannt, die mit einem Polyesterharzfilm, insbesondere aus Polyethylenterephthalat (PET), beschichtet sind. Die Beschichtung der Weißblechoberfläche mit dem Polyesterharzfilm erfolgt dabei durch Auflaminieren einer Polyesterfolie, insbesondere einer PET-Folie, auf die Oberfläche des Weißblechs. Um eine ausreichende Haftung des Polyesterharzfilms auf der Weißblechoberfläche zu gewährleisten, wird auf der Weißblechoberfläche vor dem Auflaminieren des Polyesterharzfilms eine chromhaltige Haftschicht aufgebracht, welche beispielsweise durch eine Monolage von hydratisiertem Chromoxid oder durch eine Doppellage von metallischem Chrom mit einer darüberliegenden Lage von hydratisiertem Chromoxid gebildet wird. Ohne diese Haftschicht zwischen der Weißblechoberfläche und dem Polyesterharzfilm würde sich der Polyesterharzfilm, insbesondere ein PET-Film, von dem Weißblech ablösen, insbesondere bei Umformungen in den Verfahren zur Herstellung von Verpackungen oder beim Sterilisieren oder Befüllen der Verpackungen mit heißen Füllgütern. Die für die Herstellung der chromhaltigen Haftschicht verwendeten Chromverbindungen sind jedoch giftig und umweltgefährdend.From the publications DE 40 09 839 A1 . DE 34 36 412 C2 and EP 664 209 A1 Tinned steel sheets are known, which are coated with a polyester resin film, in particular of polyethylene terephthalate (PET). The coating of the tinplate surface With the polyester resin film is carried out by laminating a polyester film, in particular a PET film, on the surface of the tinplate. In order to ensure sufficient adhesion of the polyester resin film to the tinplate surface, a chromium-containing adhesive layer is applied to the tinplate surface prior to laminating the polyester resin film, formed for example by a monolayer of hydrated chromium oxide or by a double layer of metallic chromium with an overlying layer of hydrated chromium oxide , Without this adhesive layer between the tinplate surface and the polyester resin film, the polyester resin film, especially a PET film, would peel off the tinplate, particularly in forming processes in the packaging manufacturing processes or in sterilizing or filling the packages with hot fillers. However, the chromium compounds used for the preparation of the chromium-containing adhesive layer are toxic and environmentally hazardous.

Als alternativer Werkstoff für Weißblech ist aus dem Stand der Technik elektrolytisch verchromtes Stahlblech (Electrolytic Chromium Coated Steel; ECCS) bekannt. Bei diesem Werkstoff, der auch als "Tin-Free Steel (TFS)" bezeichnet wird, handelt es sich um kaltgewalztes Stahlblech, welches elektrolytisch mit einer Beschichtung aus Chrom und Chromoxid versehen worden ist. Die Oberfläche dieses Werkstoffs weist eine gute Haftung für Polymermaterialien auf, wie z.B. für Polyethylenterephthalat oder Polypropylen, und kann daher mit diesen Polymeren beschichtet werden, beispielsweise durch Auflaminieren einer Polymerfolie, um einen zusätzlichen Korrosionsschutz zu ermöglichen. Die Haftung der Polymerbeschichtung auf der Chrom-Oberfläche des ECCS bzw. TFS hält dabei auch starken Umformungen, wie sie beispielsweise bei der Herstellung von Verpackungsbehältern auftreten, sowie Sterilisationsprozessen stand. Mit Polymerbeschichtungen versehene ECCS-Bleche werden deshalb insbesondere in Herstellungsverfahren für Behälter verwendet, in denen starke Verformungen der Bleche erforderlich sind, wie z.B. bei der Herstellung von Ventiltellern für Aerosoldosen, wobei die organische Beschichtung beim ECCS vor der Umformung erfolgt, weil andernfalls starker Werkzeugverschleiß auf tritt.As an alternative material for tinplate, electrolytic chromium coated steel (ECCS) is known from the prior art. This material, also known as "Tin-Free Steel (TFS)", is a cold-rolled steel sheet which has been electrolytically coated with a coating of chromium and chromium oxide. The surface of this material has good adhesion to polymeric materials, e.g. for polyethylene terephthalate or polypropylene, and therefore can be coated with these polymers, for example by laminating a polymeric film to allow additional corrosion protection. The adhesion of the polymer coating on the chromium surface of the ECCS or TFS also holds strong transformations, such as occur in the production of packaging containers, as well as sterilization processes stood. Polymer coated ECCS sheets are therefore particularly used in manufacturing processes for containers in which severe deformation of the sheets is required, e.g. in the manufacture of valve plates for aerosol cans, wherein the organic coating in the ECCS before forming takes place, otherwise severe tool wear occurs.

Aus der EP 848 664 B1 ist beispielsweise ein durch eine Chrombeschichtung gegen Korrosion geschütztes Stahlband (ECCS bzw. TFS) bekannt, auf dem ein Film aus Polyethylenterephthalat auflaminiert worden ist. Derartige Stahlbleche, welche mit einer Chrombeschichtung gegen Korrosion geschützt sind, erweisen sich jedoch ebenfalls wegen der Toxizität der im Herstellungsprozess verwendeten Chromverbindungen, insbesondere der flüssigen Chromsäure (Chrom VI) des Veredelungsbades, als nachteilig.From the EP 848 664 B1 For example, a steel strip protected by a chromium coating against corrosion (ECCS or TFS) on which a film of polyethylene terephthalate has been laminated is known. However, such steel sheets, which are protected with a chromium coating against corrosion, but also prove because the toxicity of the chromium compounds used in the manufacturing process, in particular the liquid chromic acid (chromium VI) of the finishing bath, as disadvantageous.

Aus der WO 97/03823-A ist ein korrosionsbeständiges Stahlblech bekannt, welches eine metallische Korrosionsschutzschicht aufweist, bei der es sich bspw. um elektrolytisch aufgebrachte Zinn- oder Chrom-/Chromoxidschichten handeln kann, auf denen ein- oder beidseitig ein transparenter Polymerfilm durch Auflaminieren einer Polymerfolie aufgebracht wird. Der Polymerfilm besteht dabei aus Polyethylenterephthalat (PET), Polyvinylchlorid (PVC) oder aus Polypropylen (PP).From the WO 97/03823-A a corrosion-resistant steel sheet is known, which has a metallic corrosion protection layer, which may be, for example, electrolytically applied tin or chromium / chromium oxide layers on which one or both sides a transparent polymer film is applied by laminating a polymer film. The polymer film consists of polyethylene terephthalate (PET), polyvinyl chloride (PVC) or polypropylene (PP).

Zwischen der metallischen Korrosionsschutzschicht des Stahlblechs und dem auflaminierten Polymerfilm ist dabei ein Haftvermittler, insbesondere eine Haftschicht vorgesehen. Zur Herstellung des korrosionsbeständigen Stahlblechs wird ein galvanisch mit einer metallischen Korrosionsschutzschicht beschichtetes und passiviertes Stahlblech mit einer Dicke zwischen 0,05 mm und 0,5 mm verwendet und auf Temperaturen von ca. 160°C erhitzt. Auf das erhitzte Stahlblech wird mittels rotierender Rollen die Polymerfolie auflaminiert. Die Dicke des auflaminierten Polymerfilms liegt zwischen 5 und 100 µm. Die Polymerfolie weist dabei bevorzugt auf einer Seite eine Haftschicht auf, welche einen niedrigeren Schmelzpunkt hat als das Polymermaterial der Polymerfolie. Der Polymerfilm wird mit der Haftschicht auf die Oberfläche der metallischen Korrosionsschutzschicht des Stahlblechs hin orientiert auflaminiert.In this case, an adhesion promoter, in particular an adhesive layer, is provided between the metallic corrosion protection layer of the steel sheet and the laminated polymer film. To produce the corrosion-resistant steel sheet, a galvanically coated with a metallic corrosion protection layer and passivated steel sheet with a thickness between 0.05 mm and 0.5 mm is used and heated to temperatures of about 160 ° C. On the heated steel sheet, the polymer film is laminated by means of rotating rollers. The thickness of the laminated polymer film is between 5 and 100 microns. The polymer film preferably has on one side an adhesive layer which has a lower melting point than the polymer material of the polymer film. The polymer film is laminated with the adhesive layer on the surface of the metallic corrosion protection layer of the steel sheet oriented.

In diesem Verfahren zum Auflaminieren einer Polymerfolie auf die metallische Korrosionsschutzschicht eines Stahlblechs wird eine spezielle Polymerfolie mit einer Haftschicht verwendet, um die Polymerfolie auf die Oberfläche der Korrosionsschutzschicht des Stahlblechs zu laminieren. Solche Polymerfolien mit einer Haftschicht sind in der Herstellung sehr teuer. Ferner ist die Handhabung solcher Polymerfolien mit einer Haftschicht aufwendiger und die Verfahrensparameter, insbesondere die Temperaturen, müssen beim Auflaminieren innerhalb der vorgegebenen Grenzwerte gehalten werden, welche durch die Schmelztemperaturen der Polymerfolie und der Haftschicht bestimmt sind. Insbesondere bei verzinnten Stahlblechen hat sich jedoch gezeigt, dass auf eine Haftschicht nicht verzichtet werden kann, wenn eine ausreichend gute Haftung des Polymerfilms auf der verzinnten Oberfläche des Stahlblechs gewährleistet werden soll. Auf den Chromoberflächen von ECCS bzw. TFS haften die Polymerfolien dagegen besser, allerdings fallen bei der Herstellung von ECCS wegen der bei der Beschichtung des Stahlblechs verwendeten chromhaltigen Substanzen giftige und umweltschädliche Abfälle an.In this method of laminating a polymer film on the metallic anticorrosion layer of a steel sheet, a special polymer film having an adhesive layer is used to laminate the polymer film on the surface of the anticorrosion layer of the steel sheet. Such polymer films with an adhesive layer are very expensive to manufacture. Furthermore, the handling of such polymer films with an adhesive layer is more complicated and the process parameters, in particular the temperatures, must be kept during the lamination within the predetermined limits, which are determined by the melting temperatures of the polymer film and the adhesive layer. In particular, with tin-plated steel sheets, however, it has been found that an adhesive layer can not be dispensed with if sufficiently good adhesion of the polymer film to the tinned surface of the steel sheet is to be ensured. On the chrome surfaces of ECCS and TFS, however, the polymer films adhere better, but fall in the production of ECCS, because of the chromium-containing substances used in the coating of the steel sheet, toxic and polluting waste.

Hiervon ausgehend liegt der Erfindung die Aufgabe zugrunde, ein möglichst vollständig chromfreies Verfahren zur Herstellung eines hochkorrosionsbeständigen Stahlblechs aufzuzeigen. Das mit dem Verfahren hergestellte hochkorrosionsbeständige Stahlblech soll insbesondere für die Herstellung von Verpackungen geeignet sein und auch bei starken Umformungen im Herstellungsprozess und einer Sterilisierung der hergestellten Verpackung keine Beeinträchtigung hinsichtlich der Korrosionsbeständigkeit erleiden.Proceeding from this, the object of the invention is to provide a method which is as completely as possible free of chromium for the production of a highly corrosion-resistant steel sheet. The highly corrosion-resistant steel sheet produced by the method should be suitable in particular for the production of packaging and suffer no deterioration in terms of corrosion resistance even with severe deformations in the manufacturing process and sterilization of the package produced.

Diese Aufgaben werden mit dem Verfahren gemäß Anspruch 1 sowie durch ein mit einer Polymerbeschichtung versehenes Weißblech mit den Merkmalen des Anspruchs 7 gelöst. Bevorzugte Ausführungsformen der Verfahren sind in den abhängigen Ansprüchen 2 - 6 aufgezeigt und die abhängigen Ansprüche 8 - 11 stellen bevorzugte Ausführungsformen des Weißblechs dar. Anspruch 12 zeigt Verwendungen des mit einer Polymerbeschichtung versehenen Weißblechs auf und in Anspruch 13 ist eine Vorrichtung zur Durchführung des erfindungsgemäßen Verfahrens angegeben.These objects are achieved by the method according to claim 1 and by a provided with a polymer coating tinplate having the features of claim 7. Preferred embodiments of the methods are set out in the dependent claims 2-6 and the dependent claims 8-11 represent preferred embodiments of the tinplate. Claim 12 shows uses of the tinplate provided with a polymer coating and in claim 13 is an apparatus for carrying out the method according to the invention specified.

In dem erfindungsgemäßen Verfahren zum Beschichten einer chromfreien Oberfläche eines verzinnten Stahlblechs (Weißblechs) mit einer Polymerbeschichtung wird die chromfreie Zinnoberfläche des verzinnten Stahlblechs zunächst in einem ersten Schritt elektrochemisch oxidiert und in einem zweiten Schritt wird auf die oxidierte Zinnoberfläche eine Polymerbeschichtung aufgebracht. Durch die elektrochemische Oxidation der Zinnoberfläche wird eine chromfreie Passivierung der Zinnoberfläche gewährleistet, welche ein ungehindertes Anwachsen von Zinnoxid auf der Weißblechoberfläche verhindert. Anders als bei den bekannten Verfahren zur Passivierung von Weißblech gegen das Anwachsen von Zinnoxid auf der Weißblechoberfläche erfolgt die Passivierung der Weißblechoberfläche in dem erfindungsgemäßen Verfahren ohne Verwendung von chromhaltigen Substanzen, insbesondere ohne die Verwendung von giftigen und umweltgefährdenden Chromoxiden. Es wurde in überraschender Weise festgestellt, dass diese chromfreie Passivierung der Weißblechoberfläche durch elektrochemische Oxidation nicht nur ein ungehindertes Anwachsen von Zinnoxid auf der Weißblechoberfläche verhindert, sondern gleichzeitig auch eine gute Haftgrundlage für Polymere bildet. Dadurch kann in dem zweiten Schritt des erfindungsgemäßen Verfahrens problemlos eine Polymerbeschichtung auf die oxidierte Zinnoberfläche des Weißblechs aufgebracht werden, wobei die oxidierte Zinnoberfläche eine sehr gute Haftung der Polymerbeschichtung ermöglicht. Es hat sich gezeigt, dass die Haftung zwischen der oxidierten Zinnoberfläche und der Polymerbeschichtung auch starken Umformungen standhält, wie sie beispielsweise in Verfahren zur Herstellung von mehrfach tiefgezogenen Dosen oder bei der Herstellung von Ventiltellern auftreten. Die Haftung zwischen der oxidierten Zinnoberfläche und der Polymerbeschichtung hält auch ohne Weiteres einer Sterilisation stand, ohne dass es während der Sterilisation zu einem Ablösen der Polymerbeschichtung von der Weißblechoberfläche kommen kann.In the method according to the invention for coating a chromium-free surface of a tinned steel sheet (tinplate) with a polymer coating, the chromium-free tin surface of the tinned steel sheet is first electrochemically oxidized in a first step and in a second step a polymer coating is applied to the oxidized tin surface. The electrochemical oxidation of the tin surface ensures chromium-free passivation of the tin surface, which prevents unhindered growth of tin oxide on the tinplate surface. Unlike the known methods for passivating tinplate against the growth of tin oxide on the tinplate surface, the passivation of the tinplate surface takes place in the process according to the invention without the use of chromium-containing substances, in particular without the use of toxic and environmentally hazardous chromium oxides. It has surprisingly been found that this chromium-free passivation of the tinplate surface by electrochemical oxidation not only prevents unhindered growth of tin oxide on the tinplate surface, but at the same time also forms a good adhesion base for polymers. As a result, in the second step of the process according to the invention, a polymer coating can easily be oxidized onto the Tin surface of the tinplate are applied, the oxidized tin surface allows a very good adhesion of the polymer coating. It has been found that the adhesion between the oxidized tin surface and the polymer coating also withstands severe deformation, as occurs, for example, in processes for the production of multi-deep-drawn cans or in the manufacture of valve plates. The adhesion between the oxidized tin surface and the polymer coating also readily withstands sterilization, without any detachment of the polymer coating from the tinplate surface during sterilization.

In dem erfindungsgemäßen Verfahren zur Herstellung eines mit einer Polymerbeschichtung beschichteten Weißblechs wird in einem ersten Verfahrensschritt zunächst auf eine oder beide Seiten eines Stahlblechs eine Zinnbeschichtung elektrolytisch abgeschieden. In einem zweiten Schritt erfolgt eine elektrochemische Oxidation der Oberfläche der Zinnbeschichtung und schließlich wird auf die oxidierte Oberfläche der Zinnbeschichtung eine Polymerbeschichtung aufgebracht. Die elektrochemische Oxidation der Zinnoberfläche erfolgt dabei bevorzugt unmittelbar und insbesondere innerhalb weniger Sekunden nach dem Abscheiden der Zinnbeschichtung auf das Stahlblech. Die elektrochemische Oxidation der Zinnoberfläche erfolgt hierbei bevorzugt auch ohne weitere Zwischenschritte, insbesondere ohne eine Zwischenreinigung oder eine Temperaturbehandlung der Weißblechoberfläche.In the process according to the invention for producing a tinplate coated with a polymer coating, in a first process step, first of all, a tin coating is deposited electrolytically on one or both sides of a steel sheet. In a second step, an electrochemical oxidation of the surface of the tin coating takes place and finally a polymer coating is applied to the oxidized surface of the tin coating. The electrochemical oxidation of the tin surface is preferably carried out directly and in particular within a few seconds after the deposition of the tin coating on the steel sheet. The electrochemical oxidation of the tin surface preferably takes place here without further intermediate steps, in particular without intermediate cleaning or temperature treatment of the tinplate surface.

Die elektrochemische Oxidation der Zinnoberfläche kann insbesondere durch anodische Polarisation des verzinnten Stahlblechs in einem wässrigen und chromfreien Elektrolyten erfolgen. Beispielweise kann die elektrochemische Oxidation der Zinnoberfläche durch Eintauchen des Weißblechs in eine Soda-Lösung (Natriumcarbonatlösung) durchgeführt werden. Dabei bildet sich an der (chromfreien) Zinnoberfläche des Weißblechs eine dünne Zinnoxidschicht aus, welche im Wesentlichen aus vierwertigem Zinnoxid (SnO2) besteht. Dieses vierwertige Zinnoxid ist gegenüber zweiwertigem Zinnoxid (SnO), welches bei Lagerung von Weißblech in sauerstoffhaltiger Atmosphäre an der Weißblechoberfläche entsteht, wesentlich inerter und verhindert ein ungehindertes Anwachsen einer (zweiwertigen) Zinnoxidschicht auf der Weißblechoberfläche bei Kontakt mit Sauerstoff. Die Dicke der bei der elektrochemischen Oxidation der Weißblechoberfläche entstehenden Oxidschicht aus im Wesentlichen vierwertigem Zinnoxid liegt zweckmäßig im nm-Bereich und ist bevorzugt dünner als 100 nm. Bei der Ausbilduung dieser passivierenden Zinnoxidschicht auf der Weißblechoberfläche wird in dem Schritt der elektrochemischen Oxidation bevorzugt eine Ladungsdichte auf der Zinnoberfläche erzeugt, die höchstens 40 C/m2 beträgt.The electrochemical oxidation of the tin surface can be carried out in particular by anodic polarization of the tinned steel sheet in an aqueous and chromium-free electrolyte. For example, the electrochemical oxidation of the tin surface may be carried out by immersing the tinplate in a soda solution (sodium carbonate solution). In this case, a thin tin oxide layer, which consists essentially of tetravalent tin oxide (SnO 2 ), forms on the (chromium-free) tin surface of the tinplate. This tetravalent tin oxide is significantly more inert than divalent tin oxide (SnO), which is formed on the tinplate surface when tinplate is stored in an oxygen-containing atmosphere, and prevents unhindered growth of a (divalent) tin oxide layer on the tinplate surface upon contact with oxygen. The thickness of the oxide layer of essentially tetravalent tin oxide formed during the electrochemical oxidation of the tinplate surface is expediently in the nm range and is preferably thinner than 100 nm. In the formation of this passivating tin oxide layer on the Tinplate surface is preferably generated in the step of electrochemical oxidation, a charge density on the tin surface, which is at most 40 C / m 2 .

Nach der elektrochemischen Oxidation der Weißblechoberfläche wird diese mit einer Polymerbeschichtung versehen, wobei die Polymerbeschichtung zweckmäßig eine Dicke im Bereich von 10 bis 100 µm hat und bevorzugt durch Auflaminieren einer Polymerfolie auf die oxidierte Zinnoberfläche aufgebracht wird. Besonders zweckmäßig ist hierbei die Verwendung einer coextrudierten Kunststofffolie mit einer Polymerschicht und einer Haftvermittlerschicht, welche auf die oxidierte Zinnoberfläche des Stahlblechs auflaminiert wird, indem die Haftvermittlerschicht der Kunststofffolie auf die oxidierte Zinnoberfläche aufgelegt und unter Hitzeeinwirkung mittels Laminierwalzen bzw. Laminierrollen auflaminiert wird. Durch die Haftvermittlerschicht wird die an sich schon gute Haftung der Polymerbeschichtung auf der oxidierten Zinnoberfläche des Weißblechs noch erhöht.After the electrochemical oxidation of the tinplate surface, this is provided with a polymer coating, wherein the polymer coating expediently has a thickness in the range of 10 to 100 microns and is preferably applied by laminating a polymer film on the oxidized tin surface. The use of a coextruded plastic film with a polymer layer and an adhesion promoter layer, which is laminated to the oxidized tin surface of the steel sheet, by applying the adhesion promoter layer of the plastic film to the oxidized tin surface and laminating it under the action of heat by means of laminating rolls or lamination rolls is particularly expedient. The adhesion promoter layer further increases the inherently good adhesion of the polymer coating to the oxidized tin surface of the tinplate.

Als besonders zweckmäßig hat es sich erwiesen, wenn das verzinnte Stahlblech während des Auflaminierens der Polymerfolie auf Temperaturen oberhalb der Schmelztemperatur der Zinnbeschichtung (232°C) erwärmt wird. Dadurch wird die Zinnbeschichtung des Weißblechs aufgeschmolzen, so dass zumindest die oberflächennahen Bereiche der Zinnbeschichtung des Weißblechs während des Auflaminierens der Polymerfolie im schmelzflüssigen Zustand vorliegen. Dadurch wird die Haftung zwischen der (schmelzflüssigen) Zinnoberfläche des Stahlblechs und der auflaminierten Polymerbeschichtung noch verbessert. Insbesondere kann dadurch auch bei Verwendung von Polymermaterialien der Polymerbeschichtung mit einem Schmelzpunkt von mehr als 232°C oder bei Verwendung von coextrudierten Kunststofffolien mit einer Haftvermittlerschicht, deren Schmelzpunkt größer als 232°C ist, eine ausreichende Haftung zwischen der Polymerbeschichtung und der Zinnoberfläche des Weißblechs gewährleistet werden. Besonders bevorzugt ist es allerdings, wenn das Stahlblech beim Auflaminieren der Polymerfolie auf die verzinnte Oberfläche auf Temperaturen erhitzt wird, die sowohl höher als die Schmelztemperatur des Zinns als auch höher als die Schmelztemperatur des für die Ausbildung der Polymerbeschichtung verwendeten Polymermaterials oder des ggf. vorhanden Haftvermittlers sind.It has proven particularly expedient if the tinned steel sheet is heated to temperatures above the melting temperature of the tin coating (232 ° C.) during the lamination of the polymer film. As a result, the tin coating of the tinplate is melted, so that at least the near-surface areas of the tin coating of the tinplate are in the molten state during the lamination of the polymer film. This further improves the adhesion between the (molten) tin surface of the steel sheet and the laminated polymer coating. In particular, even when using polymer materials of polymer coating having a melting point of more than 232 ° C or when using coextruded plastic films with a primer layer whose melting point is greater than 232 ° C, sufficient adhesion between the polymer coating and the tin surface of the tinplate ensured become. However, it is particularly preferred if the steel sheet is heated to temperatures on the tinned surface during the lamination of the polymer film which are both higher than the melting temperature of the tin and higher than the melting temperature of the polymer material used for the formation of the polymer coating or of the adhesion promoter which may be present are.

Es ist auch möglich, eine Polymerbeschichtung ohne einen zusätzlichen Haftvermittler auf die oxidierte Zinnoberfläche des Weißblechs aufzubringen. Nur wenn in den nachfolgenden Verarbeitungsprozessen bei der Verarbeitung des erfindungsgemäß hergestellten Weißblechs sehr starke Umformungen vorgenommen werden, ist die Verwendung eines Haftvermittlers zwischen der oxidierten Zinnoberfläche des Weißblechs und der Polymerbeschichtung erforderlich, um ein Ablösen der Polymerbeschichtung bei den Umformschritten zu verhindern.It is also possible to apply a polymer coating without an additional adhesion promoter to the oxidized tin surface of the tinplate. Only if in the subsequent processing in the processing of the tinplate according to the invention very strong transformations are made, the use of an adhesion promoter between the oxidized tin surface of the tinplate and the polymer coating is required to prevent detachment of the polymer coating in the forming steps.

Für besondere Anwendungen des erfindungsgemäß hergestellten Weißblechs, in denen hohe Umformraten mit Tiefziehraten von D/d = β = 1,7 (D = Rondendurchmesser; d = Napfdurchmesser) und höher erforderlich sind, hat sich die Verwendung eines Haftvermittlers zwischen der Polymerbeschichtung und der Zinnoberfläche des Weißblechs als zweckmäßig erwiesen. Als geeignete Haftvermittler haben sich Zwischenschichten erwiesen, die glykolmodifiziertes Polyethylenterephthalat (PETG), glykolmodifziertes Polyzyklohexylendimethylenterephtalat (PCTG) und/oder Isophthalsäure (IPA) oder Gemische davon enthalten.For special applications of the tinplate according to the invention, in which high forming rates with deep-drawing rates of D / d = β = 1.7 (D = diameter of the tube, d = bowl diameter) and higher are required, the use of a coupling agent between the polymer coating and the tin surface has become necessary of the tinplate proved to be useful. Intermediate layers which comprise glycol-modified polyethylene terephthalate (PETG), glycol-modified polycyclohexylenedimethylene terephthalate (PCTG) and / or isophthalic acid (IPA) or mixtures thereof have proven suitable adhesion promoters.

Bei dem Polymermaterial der Polymerbeschichtung handelt es sich zweckmäßig um einen thermoplastischen Polyester, insbesondere um Polyethylenterephthalat (PET). Der Schmelzpunkt von Polyethylenterephthalat liegt im Bereich von 260 - 270°C. Um beim Aufbringen der Polymerbeschichtung auf die oxidierte Zinnoberfläche eine möglichst gute Haftung zu gewährleisten ist es zweckmäßig, das verzinnte Stahlblech beim Aufbringen der Polymerbeschichtung auf Temperaturen oberhalb des Schmelzpunkts von Polyethylenterephthalat zu erwärmen, so dass beim Aufbringen der Polymerbeschichtung sowohl die Zinnoberfläche des Weißblechs als auch zumindest die dem Weißblech zugewandten oberflächennahen Bereiche der Polymerbeschichtung im schmelzflüssigen Zustand vorliegen und dadurch eine innige Materialverbindung eingehen können. Es hat sich als besonders zweckmäßig erwiesen, wenn das verzinnte Stahlblech beim Aufbringen der Polymerbeschichtung im Temperaturbereich zwischen 270°C und 290°C und bevorzugt auf ca. 280°C gehalten wird.The polymer material of the polymer coating is expediently a thermoplastic polyester, in particular polyethylene terephthalate (PET). The melting point of polyethylene terephthalate is in the range of 260-270 ° C. In order to ensure the best possible adhesion when applying the polymer coating to the oxidized tin surface, it is expedient to heat the tinned steel sheet to temperatures above the melting point of polyethylene terephthalate when the polymer coating is applied, so that both the tin surface of the tinplate and at least when the polymer coating is applied the near-surface areas of the polymer coating facing the tinplate are in the molten state and can therefore form an intimate material connection. It has proven to be particularly useful if the tinned steel sheet during application of the polymer coating in the temperature range between 270 ° C and 290 ° C and preferably maintained at about 280 ° C.

Um beispielsweise beim Auflaminieren einer Polymerfolie auf die oxidierte Zinnoberfläche des Stahlblechs mittels Laminierwalzen ein Ankleben der Polymerfolie an den beheizten Laminierwalzen zu verhindern, wird zweckmäßig eine mehrschichtige Kunststofffolie zur Ausbildung der Polymerbeschichtung verwendet, welche auf ihrer Oberseite eine Antiblockschicht aufweist. Eine solche Antiblockschicht kann beispielsweise durch eine Siliziumoxid-Schicht auf der Oberseite der Polymerfolie gebildet sein.For example, in order to prevent sticking of the polymer film to the heated laminating rollers when laminating a polymer film onto the oxidized tin surface of the steel sheet by means of laminating rollers, it is expedient to use a multilayer plastic film for forming the polymer coating, which has an antiblocking layer on its upper side. Such an antiblocking layer may be formed, for example, by a silicon oxide layer on top of the polymer film.

Die erfindungsgemäßen Verfahren können in Bandverzinnungsanlagen durchgeführt werden, wobei ein Stahlband mittels einer Transporteinrichtung mit einer Bandgeschwindigkeit von bevorzugt mehr als 200 m/min und besonders bevorzugt von mehr als 500 m/min durch eine Verzinnungseinrichtung bewegt wird, um eine oder beide Seiten des Stahlbands elektrolytisch mit einer Zinnbeschichtung zu beschichten. Die nachfolgende elektrochemische Oxidation der Zinnoberfläche erfolgt in einer Oxidationseinrichtung bevorzugt durch Durchleiten des verzinnten Stahlbands mit der Bandgeschwindigkeit durch ein Elektrolysebad mit einem wässrigen Elektrolyten, wobei das Stahlband dabei zweckmäßig als Anode geschaltet wird, um die Zinnoberfläche elektrochemisch (anodisch) zu oxidieren. Danach wird auf die oxidierte Zinnoberfläche des laufenden Stahlbands in einer Kunststoffbeschichtungseinrichtung die Polymerbeschichtung aufgebracht, wozu bevorzugt mittels Laminierwalzen ein- oder beidseitig ein Polymerfilm auf die oxidierte Zinnoberfläche auflaminiert wird. Die Verzinnungseinrichtung und die Oxidationseinrichtung sind dabei in Bandlaufrichtung gesehen hintereinander und bevorzugt so nah zueinander angeordnet, dass bei den typischen Bandgeschwindigkeiten von mehr als 200 m/min innerhalb kürzester Zeit und bevorzugt innerhalb weniger Sekunden nach der Zinnbeschichtung die verzinnte Oberfläche des Stahlbands elektrochemisch oxidiert werden kann.The processes according to the invention can be carried out in strip-tinning plants in which a steel strip is moved by means of a transport device at a strip speed of preferably more than 200 m / min and more preferably of more than 500 m / min through a tinning device, around one or both sides of the steel strip electrolytically coated with a tin coating. The subsequent electrochemical oxidation of the tin surface is carried out in an oxidation device preferably by passing the tinned steel strip at the belt speed through an electrolytic bath with an aqueous electrolyte, wherein the steel strip is suitably connected as an anode to electrochemically (anodically) oxidize the tin surface. Thereafter, the polymer coating is applied to the oxidized tin surface of the running steel strip in a plastic coating device, for which purpose preferably by means of laminating rollers on one or both sides a polymer film is laminated onto the oxidized tin surface. The tinning device and the oxidation device are arranged one behind the other in the belt running direction and preferably so close to each other that at the typical belt speeds of more than 200 m / min within a very short time and preferably within a few seconds after the tin coating, the tinned surface of the steel belt can be electrochemically oxidized ,

Diese und weitere Vorteile der erfindungsgemäßen Verfahren und des erfindungsgemäßen Weißblechs ergeben sich aus den nachfolgend beschriebenen Ausführungsbeispielen, welche unter Bezugnahme auf die begleitenden Zeichnungen erläutert werden. Die Zeichnungen zeigen:

Fig. 1:
Schematische Darstellung einer Vorrichtung zur Durchführung des erfindungsgemäßen Verfahrens zur Herstellung von mit einer Polymerbeschichtung beschichtetem Weißblech;
Fig. 2:
Schematische Darstellung eines erfindungsgemäßen Weißblechs mit einer Polymerbeschichtung ohne Haftvermittlerschicht;
Fig. 3:
Schematische Darstellung eines erfindungsgemäßen Weißblechs mit einer Polymerbeschichtung mit Haftvermittlerschicht.
These and other advantages of the inventive method and the tinplate according to the invention will become apparent from the embodiments described below, which are explained with reference to the accompanying drawings. The drawings show:
Fig. 1:
Schematic representation of an apparatus for carrying out the method according to the invention for the production of coated with a polymer coating tinplate;
Fig. 2:
Schematic representation of a tinplate according to the invention with a polymer coating without adhesive layer;
3:
Schematic representation of a tinplate according to the invention with a polymer coating with a bonding agent layer.

Ausgangsmaterial für das erfindungsgemäße Verfahren zur Herstellung eines mit einer Polymerbeschichtung beschichteten Weißblechs ist bevorzugt ein warmgewalztes und un- oder niedriglegiertes Stahlblech in Bandform (Stahlband) mit geringem Kohlenstoffgehalt von bspw. 20 bis 900 ppm. Die Legierungsbestandteile des Stahls genügen zweckmäßig den Vorgaben des internationalen Standards ASTM A 623-11 (Standard Specification for Tin Mill Products), wodurch eine Verwendung der erfindungsgemäß erzeugten Weißbleche zur Herstellung von Lebensmittelverpackungen sicher gestellt wird. Grundsätzlich können für das erfindungsgemäße Verfahren alle Stahlsorten verwendet werden, welche eine für die Herstellung von Fein- oder Feinstblechen geeignete Zusammensetzung aufweisen. Das warmgewalzte Stahlband wird zunächst in einer (nicht dargestellten) Beizanlage gebeizt, danach gespült und getrocknet und anschließend in einer Kaltwalzeinrichtung kaltgewalzt. Dabei wird das Stahlband auf eine Dicke von weniger als 1,0 mm (Feinblech) und bevorzugt auf Dicken von 0,1 bis 0,5 mm (Feinstblech) gewalzt. Nach dem Kaltwalzen wird das Stahlband zunächst durch einen Durchlaufglühofen geführt, in dem das Stahlband auf Temperaturen von 550°C bis 700°C erhitzt wird, um den Stahl rekristallisierend zu Glühen. Durch das rekristallisierende Glühen wird die Umformbarkeit des kaltgewalzten Stahlbands wieder hergestellt. Nach dem Rekristallisationsglühen kann das Stahlband in einem Nachwalzwerk dressiert oder nachgewalzt werden, falls zur Erzielung der für die vorgesehenen Verarbeitungszwecke notwendigen Umformeigenschaften erforderlich. Beim Nachwalzen kann ggf. auch eine erforderliche weitere Dickenreduktion des Stahlbands erzielt werden. Nach dem Dressieren oder Nachwalzen erfolgt eine Reinigung des Stahlbands durch eine alkalische elektrolytische Behandlung und durch Beizen mit anschließendem Spülen.The starting material for the process according to the invention for the production of a polymer coating coated tinplate is preferably a hot rolled and unalloyed or low-alloyed sheet steel (steel strip) with a low carbon content of, for example, 20 to 900 ppm. The alloy components of the steel suitably meet the requirements of the international standard ASTM A 623-11 (Standard Specification for Tin Mill Products), whereby a use of the tinplates according to the invention produced for the production of food packaging is ensured. In principle, all steel grades which have a composition suitable for the production of fine or superfine sheets can be used for the method according to the invention. The hot-rolled steel strip is first pickled in a (not shown) pickling plant, then rinsed and dried and then cold-rolled in a cold rolling mill. The steel strip is rolled to a thickness of less than 1.0 mm (thin sheet) and preferably to thicknesses of 0.1 to 0.5 mm (fine sheet). After cold rolling, the steel strip is first passed through a continuous annealing furnace in which the steel strip is heated to temperatures of 550 ° C to 700 ° C to recrystallize the steel to anneal. The recrystallizing annealing reestablishes the formability of the cold rolled steel strip. After recrystallization annealing, the steel strip may be dressed or regrooved in a post-rolling mill if necessary to achieve the forming properties necessary for the intended processing purposes. When re-rolling, if necessary, a required further reduction in the thickness of the steel strip can be achieved. After the temper rolling or rolling, the steel strip is cleaned by an alkaline electrolytic treatment and by pickling with subsequent rinsing.

Anschließend wird das Stahlband 10, wie in Figur 1 schematisch dargestellt, durch eine Verzinnungseinrichtung 7 geführt. Dabei wird das Stahlband 10 als Endlosband von einer Rolle 12 abgewickelt und durch eine Transporteinrichtung 6 mit einer Bandgeschwindigkeit von bevorzugt mehr als 200 m/min und bis zu 750 m/min durch einen Tank 7a mit einem zinnhaltigen Elektrolyten bewegt und als Kathode zwischen Zinnanoden durchgeführt. Dadurch wird das Zinn der Anoden gelöst und auf dem Stahlband als Zinnbeschichtung abgeschieden. Das Zinn kann dabei in beliebiger Dicke und, falls erforderlich, auf beiden Seiten des Stahlbands 10 abgeschieden werden. Die Dicke der aufgetragenen Zinnschicht liegt regelmäßig zwischen 0,5 g/m2 und 12 g/m2. Es ist jedoch auch eine Beschichtung des Stahlbands mit dünneren oder mit dickeren Zinnschichten möglich.Subsequently, the steel strip 10, as in FIG. 1 shown schematically, guided by a tinning 7. The steel strip 10 is unwound as a continuous belt from a roll 12 and moved by a conveyor 6 at a belt speed of preferably more than 200 m / min and up to 750 m / min through a tank 7a with a tin-containing electrolyte and carried out as a cathode between tin anodes , As a result, the tin of the anodes is dissolved and deposited on the steel strip as a tin coating. The tin can be deposited in any thickness and, if necessary, on both sides of the steel strip 10. The thickness of the applied tin layer is regularly between 0.5 g / m 2 and 12 g / m 2 . However, it is also possible to coat the steel strip with thinner or thicker tin layers.

Unmittelbar nach der Beschichtung des Stahlbands mit der Zinnbeschichtung und insbesondere ohne weitere Zwischenschritte wird die Zinnoberfläche des verzinnten Stahlbands 10 in einer Oxidationseinrichtung 8 elektrochemisch oxidiert. Hierfür wird das frisch verzinnte Stahlband 10 bspw. in ein Elektrolysebad mit einem sauren, chromfreien und wässrigen Elektrolyten geleitet und als Anode geschaltet. Dadurch wird die frische Zinnoberfläche des verzinnten Stahlbands 10 anodisch polarisiert. Dabei bildet sich eine Zinnoxidschicht mit einer Schichtdicke im nm-Bereich auf der Zinnoberfläche des verzinnten Stahlbands aus, welche im Wesentlichen aus vierwertigem Zinnoxid (SnO2) besteht. Dieses vierwertige Zinnoxid ist gegenüber zweiwertigem Zinnoxid (SnO), das bei der Lagerung von verzinnten Stahlblech in einer Sauerstoffatmosphäre entsteht, wesentlich inerter. Durch diese (im Wesentlichen vierwertige und inerte) Zinnoxidschicht, die sich bei der elektrochemischen Oxidation der frisch verzinnten Oberfläche bildet, wird eine hohe Beständigkeit der verzinnten Stahlbandoberfläche gegen Korrosion und Reaktion mit Schwefel gewährleistet. Die dünne Zinnoxidschicht aus im Wesentlichen vierwertigem Zinnoxid (SnO2) verhindert insbesondere ein ungehindertes Anwachsen von weiterem (zweiwertigem) Zinnoxid bei Kontakt der verzinnten Oberfläche mit Luftsauerstoff.Immediately after the coating of the steel strip with the tin coating and in particular without further intermediate steps, the tin surface of the tin-plated steel strip 10 is electrochemically oxidized in an oxidizer 8. For this purpose, the freshly tinned steel strip 10 is, for example, passed into an electrolysis bath with an acidic, chromium-free and aqueous electrolyte and connected as an anode. Thereby, the fresh tin surface of the tinned steel strip 10 is anodically polarized. In this case, a tin oxide layer having a layer thickness in the nm range is formed on the tin surface of the tin-plated steel strip, which consists essentially of tetravalent tin oxide (SnO 2 ). This tetravalent tin oxide is much more inert to divalent tin oxide (SnO) that forms when tinned steel sheet is stored in an oxygen atmosphere. This (essentially tetravalent and inert) tin oxide layer, which forms during the electrochemical oxidation of the freshly tinned surface, ensures high resistance of the tinned steel strip surface against corrosion and reaction with sulfur. The thin tin oxide layer of essentially tetravalent tin oxide (SnO 2 ) prevents, in particular, unimpeded growth of further (bivalent) tin oxide upon contact of the tinned surface with atmospheric oxygen.

Die elektrochemische Oxidation der Zinnoberfläche erfolgt bspw. als anodische Oxidation des verzinnten Stahlbands 10 in Sodalösung, d.h. in einer wässrigen Natriumcarbonatlösung. Das verzinnte Stahlband wird hierfür weiter mit der Bandgeschwindigkeit bewegt und durch ein Elektrolysebad 8a mit einer Sodalösung geleitet. Die Konzentration von Natriumcarbonat in der Sodalösung beträgt bevorzugt 1 Gew.-% bis 10 Gew.-%, vorzugsweise 2 Gew.-% bis 8 Gew.-%, bevorzugt 3 Gew.-% bis 7 Gew.-%, vor allem 4 Gew.-% bis 6 Gew.-%, insbesondere etwa 5 Gew.-%.The electrochemical oxidation of the tin surface takes place, for example, as anodic oxidation of the tinned steel strip 10 in soda solution, i. in an aqueous sodium carbonate solution. For this purpose, the tin-plated steel strip is moved further at the strip speed and passed through an electrolytic bath 8a with a soda solution. The concentration of sodium carbonate in the soda solution is preferably 1 wt .-% to 10 wt .-%, preferably 2 wt .-% to 8 wt .-%, preferably 3 wt .-% to 7 wt .-%, especially 4 Wt .-% to 6 wt .-%, in particular about 5 wt .-%.

Die Oxidationseinrichtung 8 zur elektrochemischen Oxidation der Oberfläche der Zinnbeschichtung umfasst zweckmäßig ein Elektrolysebad 8a mit einem Vertikaltank, der mit dem Elektrolyten gefüllt ist. In der Nähe des Bodens ist innerhalb des Vertikaltanks eine Umlenkrolle angeordnet, über welche das verzinnte Stahlband 10 umgelenkt wird. Zwischen dem verzinnten Stahlband 10 und der Gegenelektrode (bspw. eine Stahl-Kathode) im Vertikaltank wird ein Potenzial angelegt. Die bei der elektrochemischen Oxidation übertragene Ladungsmenge Q liegt dabei bevorzugt unterhalb von 40 C/m2. Die im Elektrolysebad herrschende Stromdichte liegt bevorzugt im Bereich von 1,0 A/dm2 bis 3 A/dm2. Die Dicke der sich dabei ausbildenden Zinnoxidschicht ist bevorzugt geringer als 100 nm und liegt besonders bevorzugt in der Größenordnung von 10 nm.The oxidation device 8 for the electrochemical oxidation of the surface of the tin coating expediently comprises an electrolytic bath 8a with a vertical tank which is filled with the electrolyte. In the vicinity of the bottom, a deflection roller is disposed within the vertical tank, via which the tinned steel strip 10 is deflected. Between the tinned steel strip 10 and the counter electrode (eg, a steel cathode) in the vertical tank, a potential is applied. The amount of charge Q transferred during the electrochemical oxidation is preferably below 40 C / m 2 . The current density prevailing in the electrolysis bath is preferably in the range from 1.0 A / dm 2 to 3 A / dm 2 . The thickness of the thereby forming tin oxide layer is preferably less than 100 nm and is particularly preferably of the order of 10 nm.

Die Anodisierungszeit entspricht der Verweilzeit des verzinnten Stahlbands im elektrochemischen Oxidationsbad (Elektrolytbad). Diese ist durch die Länge des Elektrolytbads bzw. dessen Füllstand sowie die Anodenlänge und die Bandgeschwindigkeit vorgegeben und liegt bei den typischen Bandgeschwindigkeiten zweckmäßig im Bereich von 0,1 s bis 1 s, insbesondere zwischen 0,1 s und 0,7 s, bevorzugt im Bereich von 0,15 s bis 0,5s und idealerweise um 0,2 s. Über den Füllstand kann, in Abhängigkeit der Bandgeschwindigkeit, die Anodisierungszeit auf geeignete Werte eingestellt werden, um die bevorzugte Schichtdicke der elektrochemisch erzeugten Zinnoxidschicht auszubilden.The anodization time corresponds to the residence time of the tinned steel strip in the electrochemical oxidation bath (electrolyte bath). This is predetermined by the length of the electrolyte bath or its fill level as well as the anode length and the belt speed and is advantageously in the range of 0.1 s to 1 s, in particular between 0.1 s and 0.7 s, preferably in the typical belt speeds Range from 0.15s to 0.5s, and ideally 0.2s. The fill level can be used to set the anodization time to suitable values, depending on the belt speed, in order to form the preferred layer thickness of the electrochemically produced tin oxide layer.

Der Abstand zwischen dem Stahlband 10 und der Gegenelektrode in dem Elektrolysebad 8a wird anlagenbedingt eingestellt. Er liegt bspw. im Bereich von 3 bis 15 cm, vorzugsweise im Bereich von 5 bis 10 cm und insbesondere um 10 cm. Die Temperatur des Elektrolyten liegt vorzugsweise im Bereich von 30 bis 60 °C, insbesondere im Bereich von 35 bis 50 °C.The distance between the steel strip 10 and the counter electrode in the electrolytic 8a is set due to the system. It is, for example, in the range of 3 to 15 cm, preferably in the range of 5 to 10 cm and in particular by 10 cm. The temperature of the electrolyte is preferably in the range of 30 to 60 ° C, in particular in the range of 35 to 50 ° C.

Die Stromdichte im Elektrolysebad wird bspw. im Bereich von 1,0 bis 3 A/dm2, vorzugsweise 1,3 bis 2,8 A/dm2, und insbesondere um 2,4 A/dm2 eingestellt. Die gesamte Ladungsmenge bewegt sich dabei im Bereich zwischen 0,2 C und 0,4 C und beträgt bevorzugt bspw. 0,3 C. Die entsprechenden Ladungsdichten (bezüglich der Fläche des oxidierten Weißblechbands) liegen dabei im Bereich von 0,2 C/dm2 bis 0,4 C/dm2.The current density in the electrolysis bath is set, for example, in the range from 1.0 to 3 A / dm 2 , preferably 1.3 to 2.8 A / dm 2 , and in particular by 2.4 A / dm 2 . The total amount of charge moves in the range between 0.2 C and 0.4 C and is preferably, for example, 0.3 C. The corresponding charge densities (with respect to the surface of the oxidized tinplate strip) are in the range of 0.2 C / dm 2 to 0.4 C / dm 2 .

Das verzinnte Stahlband 10 wird nach der elektrochemischen Oxidation der Zinnoberfläche mit einer Bandgeschwindigkeit von maximal 200 m/min in eine Kunststoffbeschichtungseinrichtung 9 geführt. Da das Stahlband durch die Kunststoffbeschichtungseinrichtung nicht mit den hohen Bandgeschwindigkeiten von ca. 750 m/min durchgeführt werden kann, die beim Verzinnen des Stahlbands in der Verzinnungseinrichtung gefahren werden, ist es zweckmäßig den Verfahrensschritt der Polymerbeschichtung separat, d.h. mit vorangehendem Aufrollen des verzinnten Stahlbands zu einem Coil und Zwischenlagerung des Coils durchzuführen. Dies ist problemlos möglich, da die Zinnoberfläche aufgrund der elektrochemischen Oxidation gegen ein (weiteres) ungehindertes Anwachsen einer (zweiwertigen) Zinnoxidschicht resistent ist. Es ist jedoch auch möglich, die Polymerbeschichtung ohne Zwischenlagerung und bei durchlaufendem Stahlband direkt nach dem Verzinnen und Oxidieren der Zinnoberfläche in der Kunststoffbeschichtungseinrichtung 9 aufzubringen. Dort wird auf eine oder beide Seiten des verzinnten Stahlbands eine Polymerbeschichtung aufgebracht. Hierfür wird das Stahlband zunächst in einer Heizeinrichtung 11, welche bspw. als Induktionsheizung oder auch als Infrarot- oder Mikrowellenheizung ausgebildet sein kann, auf Temperaturen erhitzt, welche zumindest oberhalb der Schmelztemperatur des Zinns (232°C) liegen. Zweckmäßig liegt die Temperatur des Stahlbands 10 beim Aufbringen der Polymerbeschichtung auch oberhalb der Schmelztemperatur des Polymermaterials. Bevorzugt handelt es sich bei dem Polymermaterial um Polyethylenterephthalat (PET mit einer Schmelztemperatur von ca. zwischen 235 und 260 °C, abhängig vom Kristallisationsgrad und vom Polymerisationsgrad) oder Polypropylen (PP mit einer Schmelztemperatur von ca. 160 °C) oder auch PE (mit einer Schmelztemperatur von ca. 130 - 145 °C).The tin-plated steel strip 10 is guided into a plastic coating device 9 after the electrochemical oxidation of the tin surface at a maximum strip speed of 200 m / min. Since the steel strip can not be performed by the plastic coating device with the high belt speeds of about 750 m / min, which are driven in tinning the steel strip in the tinning, it is appropriate to the process step of the polymer coating separately, ie with preceding rolling of the tinned steel strip to perform a coil and intermediate storage of the coil. This is easily possible since the tin surface is resistant to a (further) unhindered growth of a (divalent) tin oxide layer due to the electrochemical oxidation. However, it is also possible, the polymer coating without intermediate storage and durchlaufendem Apply steel strip directly after tinning and oxidizing the tin surface in the plastic coating device 9. There, a polymer coating is applied to one or both sides of the tinned steel strip. For this purpose, the steel strip is first heated in a heater 11, which may be formed, for example. As induction heating or as infrared or microwave heating, to temperatures which are at least above the melting temperature of the tin (232 ° C). Suitably, the temperature of the steel strip 10 during application of the polymer coating is also above the melting temperature of the polymer material. The polymer material is preferably polyethylene terephthalate (PET having a melting point of approx. Between 235 and 260 ° C., depending on the degree of crystallization and the degree of polymerization) or polypropylene (PP having a melting temperature of approx. 160 ° C.) or PE (with a melting temperature of about 130-145 ° C).

Beim Erhitzen des verzinnten Stahlbands auf Temperaturen oberhalb des Zinnschmelzpunkts bildet sich zwischen der Stahlbandoberfläche und der Zinnschicht eine dünne und sehr dichte Legierungsschicht aus, welche aus Eisenatomen des Stahls und Zinnatomen der Zinnbeschichtung besteht. Diese Legierungsschicht führt zu einer sehr guten Haftung der Zinnbeschichtung an der Stahlbandoberfläche und stellt darüber hinaus eine sehr wirksame Korrosionsbarriere dar. Bei einem vollständigen Aufschmelzen der Zinnbeschichtung wird weiterhin auch eine glänzende Oberfläche der Zinnschicht erzeugt.When the tin-plated steel strip is heated to temperatures above the tin melting point, a thin and very dense alloy layer consisting of iron atoms of the steel and tin atoms of the tin coating is formed between the steel strip surface and the tin layer. This alloy layer leads to a very good adhesion of the tin coating on the steel strip surface and also represents a very effective corrosion barrier. In a complete melting of the tin coating also a glossy surface of the tin layer is produced.

Dem erhitzten Stahlband 10 wird in der Kunststoffbeschichtungseinrichtung 9 ein- oder beidseitig eine Folie 16 aus einem Polymermaterial zugeführt und mittels (zweckmäßig beheizter) Laminierwalzen 9a an die Oberfläche der Zinnbeschichtung angedrückt. Es kann sich bei der Polymerfolie 16 um eine Folie aus einem Polyester wie Polyethylenterephthalat und insbesondere um eine biaxial orientierte oder amorphe Polyesterfolie oder um eine Folie aus Polypropylen oder auch um eine Folie aus einem Polymerlaminat bestehend aus Polyethylenterephthalat und Polypropylen und Polyethylen handeln. Falls erforderlich wird eine Polymerfolie mit einer Haftvermittlerschicht verwendet, was nachfolgend noch beschrieben wird. Aufgrund der Temperatur des erhitzten Stahlbands 10 schmilzt dabei zumindest der oberflächennahe Bereich der Zinnbeschichtung und (je nach der gewählten Temperatur des Stahlbands) ggf. auch wenigstens der dem verzinnten Stahlband 10 zugewandte Bereich der Polymerfolie 16, welcher dann beim Andrücken durch die Laminierwalzen 9a an der oxidierten Oberfläche der Zinnbeschichtung anhaftet.The heated steel strip 10 is supplied in the plastic coating device 9 on one or both sides of a film 16 made of a polymer material and pressed by (suitably heated) laminating rollers 9a to the surface of the tin coating. The polymer film 16 may be a film of a polyester such as polyethylene terephthalate and in particular a biaxially oriented or amorphous polyester film or a film of polypropylene or else a film of a polymer laminate consisting of polyethylene terephthalate and polypropylene and polyethylene. If necessary, a polymer film having a primer layer is used, which will be described later. Due to the temperature of the heated steel strip 10, at least the near-surface region of the tin coating and (depending on the selected temperature of the steel strip) possibly also at least the region of the polymer film 16 facing the tinned steel strip 10, which then presses against the lamination rolls 9a at the oxidized surface of the tin coating adheres.

Um beim Auflaminieren der Polymerfolie 16 auf die oxidierte Zinnoberfläche des Stahlblechs 10 mittels der Laminierwalzen 9a ein Ankleben der Polymerfolie an den ggf erhitzten Laminierwalzen zu verhindern, wird zweckmäßig eine mehrschichtige Polymerfolie 16 zur Ausbildung der Polymerbeschichtung verwendet, welche auf ihrer Oberseite eine Antiblockschicht aufweist. Eine solche Antiblockschicht kann beispielsweise durch eine Siliziumoxid-Schicht auf der Oberseite der Polymerfolie gebildet sein.In order to prevent sticking of the polymer film to the optionally heated laminating rollers when laminating the polymer film 16 onto the oxidized tin surface of the steel sheet 10 by means of the laminating rollers 9a, it is expedient to use a multilayer polymer film 16 for forming the polymer coating, which has an antiblocking layer on its upper side. Such an antiblocking layer may be formed, for example, by a silicon oxide layer on top of the polymer film.

Nach dem Auflaminieren der Polymerfolie erfährt das zinn- und polymerbeschichtete Stahlband 10 eine Abkühlung auf ca. 20°C. Danach kann die Polymerbeschichtung optional noch vollständig aufgeschmolzen und dann in einer Kühleinrichtung 15 (bspw. einem Wasserbad) auf eine Temperatur unterhalb des Glasübergangspunkts abgeschreckt werden. Dadurch bildet sich bspw. bei Verwendung von PET oder PP als Polymermaterial eine amorphe Struktur in dem Polyethylenterephthalat bzw. eine minimale kristalline Struktur in dem Polypropylen aus. Das Aufschmelzen der Polymerbeschichtung erfolgt dabei besonders zweckmäßig durch ein nochmaliges Erhitzen des Stahlbands 10 auf Temperaturen oberhalb des Schmelzpunkts des verwendeten Polymermaterials in einer Aufschmelzeinrichtung 14. Das Aufschmlezen der Polymerbeschichtung erfolgt in der Aufschmelzeinrichtung 14 zweckmäßig durch induktives Erhitzen des Stahlbands 10 in einer Induktionsspule 14a. Durch diese Nacherwärmung werden Eigenspannungen in der Polymerbeschichtung durch Relaxation abgebaut, was zu einer Erhöhung der Haftung zwischen der Zinnbeschichtung und der Polymerbeschichtung und dadurch zu einer Stabilisierung des Verbunds dieser Schichten führt. Bei Verwendung von PET als Polymermaterial liegt bspw. die Relaxationszeit bei weniger als 0,5 Sekunden, so dass eine kurze Erhitzung der Polymerbeschichtung auf Temperaturen oberhalb der PET-Schmelztemperatur (ca. 260°C) ausreicht, um die gewünschte Relaxation herbeizuführen. Bei den typischen Bandgeschwindigkeiten von mehr als 200 m/min reicht dazu bspw. eine Induktionsspule 14a aus, die sich in der Aufschmelzeinrichtung 14 über weniger als 1 Meter längs der Bandlaufrichtung erstreckt, um damit das Stahlband 10 in diesem Abschnitt induktiv zu erhitzen und dadurch die Polymerbeschichtung aufzuschmelzen.After lamination of the polymer film, the tin and polymer coated steel strip 10 undergoes cooling to about 20 ° C. Thereafter, the polymer coating can optionally be completely melted and then quenched in a cooling device 15 (for example a water bath) to a temperature below the glass transition point. As a result, for example, when using PET or PP as the polymer material, an amorphous structure is formed in the polyethylene terephthalate or a minimal crystalline structure in the polypropylene. The melting of the polymer coating is carried out particularly expediently by re-heating the steel strip 10 to temperatures above the melting point of the polymer material used in a melting device 14. The plastic coating of the polymer coating takes place expediently in the melting device 14 by induction heating of the steel strip 10 in an induction coil 14a. As a result of this reheating, residual stresses in the polymer coating are broken down by relaxation, which leads to an increase in the adhesion between the tin coating and the polymer coating and, as a result, to a stabilization of the composite of these layers. For example, when PET is used as the polymeric material, the relaxation time is less than 0.5 seconds, so that a brief heating of the polymer coating to temperatures above the PET melt temperature (about 260 ° C) is sufficient to provide the desired relaxation. For example, at the typical belt speeds of more than 200 m / min, an induction coil 14a extends in the melting device 14 for less than 1 meter along the strip running direction, in order to heat the steel strip 10 inductively in this section, and thus the Melt polymer coating.

Das anschließende Abschrecken der aufgeschmolzenen Polymerbeschichtung in der Kühleinrichtung 15 kann bspw. durch eine Luftkühlung oder durch Eintauchen des Stahlbands in einen Tank mit Kühlflüssigkeit erfolgen. Abschließend wird das beschichtete Stahlband 10 von der Transporteinrichtung 6 auf eine Rolle 13 aufgewickelt.The subsequent quenching of the molten polymer coating in the cooling device 15 can, for example. By air cooling or by immersing the Steel bands into a tank with coolant. Finally, the coated steel strip 10 is wound on a roller 13 by the transport device 6.

In Figur 2 ist ein entsprechend hergestelltes Weißblech im Schnitt dargestellt. Dieses umfasst die Schichten Stahlblech 1, Zinnbeschichtung 2, Zinnoxidschicht 3 und die Polymerbeschichtung 4 (bspw. aus PET).In FIG. 2 a correspondingly manufactured tinplate is shown in section. This comprises the layers of steel sheet 1, tin coating 2, tin oxide layer 3 and the polymer coating 4 (for example of PET).

Die erfindungsgemäß hergestellten Weißbleche zeichnen sich durch eine hohe Korrosionsbeständigkeit aus, welche durch die metallische Korrosionsschutzschicht aus Zinn und die Polymerbeschichtung erzielt wird. Zur Korrosionsbeständigkeit trägt dabei auch die dünne Eisen-Zinn-Legierungsschicht bei, die sich beim Erhitzen des verzinnten Stahlbands auf Temperaturen oberhalb des Zinnschmelzpunkts zwischen der Stahlbandoberfläche und der Zinnschicht ausbildet. Dabei ist die Kombination dieser Korrosionsschutzschichten besonders vorteilhaft, weil durch die Polymerbeschichtung das Freiwerden von Zinnionen aus der Zinnbeschichtung bei Lufteinwirkung vermieden wird. Die erfindungsgemäß hergestellten Weißbleche sind aufgrund der Polymerbeschichtung auch inert gegenüber aggressiven und insbesondere säurehaltigen Füllgütern und eignen sich daher sehr gut für die Herstellung von Verpackungen für solche Füllgüter. Im Vergleich zu matt-grauem ECCS (TFS) weisen die erfindungsgemäßen Weißbleche aufgrund der glänzenden Oberfläche der Zinnbeschichtung, die bei einem vollständigen Aufschmelzen der Zinnbeschichtung entsteht, eine hohe Brillanz auf. Dies ist insbesondere bei der Verwendung von transparenten oder transluzenten Polymerbeschichtungen von Vorteil, weil das Weißblech dadurch eine optisch sehr ansprechende Glanz-Oberfläche aufweist. Gegenüber den bekannten Verfahren zur Herstellung von Stahlblechen, die mit einer metallischen Korrosionsschutzschicht und einer Polymerbeschichtung versehen sind, zeichnen sich die erfindungsgemäßen Verfahren weiterhin dadurch aus, dass sie vollständig chromfrei sind, d.h. es werden keinerlei chromhaltige Substanzen verwendet.The tinplates produced according to the invention are distinguished by high corrosion resistance, which is achieved by the metallic corrosion protection layer made of tin and the polymer coating. The thin iron-tin alloy layer, which is formed when the tin-plated steel strip is heated to temperatures above the tin melting point between the steel strip surface and the tin layer, also contributes to the corrosion resistance. The combination of these anticorrosive layers is particularly advantageous because the release of tin ions from the tin coating is avoided when exposed to air by the polymer coating. Because of the polymer coating, the tinplates produced according to the invention are also inert towards aggressive and, in particular, acidic filling products and are therefore very well suited for the production of packaging for such filling products. In comparison with matt-gray ECCS (TFS), the tinplates according to the invention have a high brilliance due to the glossy surface of the tin coating, which results from a complete melting of the tin coating. This is particularly advantageous when using transparent or translucent polymer coatings, because the tinplate thereby has an optically very attractive glossy surface. Compared to the known processes for the production of steel sheets, which are provided with a metallic corrosion protection layer and a polymer coating, the processes according to the invention are further characterized in that they are completely free of chromium, i. no chromium-containing substances are used.

Die erfindungsgemäß hergestellten Stahlbänder zeichnen sich weiterhin durch eine sehr gute Haftung der Polymerbeschichtung auf der Zinnbeschichtung aus, welche aufgrund der oxidierten Zinnoberfläche auch bereits ohne Haftvermittler oder zusätzliche Haftschichten erzielt wird. Die zusätzliche Verwendung von Haftvermittlerschichten zwischen der Zinnbeschichtung und der Polymerbeschichtung ist nur für besondere Anwendungen erforderlich, in denen sehr hohe Umformraten auftreten.The steel strips produced according to the invention are further distinguished by a very good adhesion of the polymer coating to the tin coating, which is already achieved without adhesion promoters or additional adhesive layers due to the oxidized tin surface. The additional use of primer layers between the tin coating and the polymer coating is only required for special applications where very high forming rates occur.

Bei kleinen Umformraten, die bspw. in der Herstellung von runden Deckeln oder Böden für Dosen auftreten und durch ein Ziehverhältnis β = D/d (bei D = Rondendurchmesser und d = Dosendurchmesser) von β < 1,2 definiert werden können, ist die Verwendung einer Haftvermittlerschicht nicht erforderlich. Bei größeren Umformungen, wie sie z.B. bei größeren Tiefzügen (bspw. bei der Herstellung von Ventiltellern) mit β > 1,7 auftreten, ist es dagegen zweckmäßig, einen Haftvermittler zu verwenden und bei noch größeren Umformraten von β > 2 (die bspw. bei einfach und mehrfach tiefgezogenen Dosen und DWI-Dosen vorkommen) erscheint ein Haftvermittler erforderlich, um ein Ablösen der Polymerbeschichtung von der Zinnoberfläche zuverlässig zu verhindern.At low forming rates, which occur, for example, in the production of round lids or bottoms for cans and can be defined by a draw ratio β = D / d (at D = ring diameter and d = can diameter) of β <1.2, the use is a bonding agent layer not required. For larger transformations, such as e.g. with larger deep draws (eg in the production of valve plates) with β> 1.7, it is expedient to use an adhesion promoter and at even larger forming rates of β> 2 (the example. In single and multiple deep-drawn cans and DWI Doses), a coupling agent appears to be required to reliably prevent peeling of the polymer coating from the tin surface.

Als geeignete Haftvermittler haben sich glykolmodifiziertes Polyethylenterephthalat (PETG, wobei weniger als 50% der Diolkomponente aus Cyclohexadimethanol besteht), glykolmodifiziertes Polycyclohexylendimethylenterephthalat (PCTG, wobei mehr als 50% der Diolkomponente aus Cyclohexadimethanol besteht) und/oder Isophthalsäure (IPA) erwiesen. Als besonders bevorzugt haben sich Haftvermittler erwiesen, die einen Anteil PETG und 5 bis 25 Vol.% IPA oder PCTG aufweisen. Zur Ausbildung einer Haftvermittlerschicht zwischen der oxidierten Zinnoberfläche des Weißblechs und der Polymerbeschichtung wird zweckmäßig eine mehrschichtige Polymerfolie verwendet, die eine Polymerschicht (bspw. aus PET) und eine Haftvermittlerschicht aus einem der oben genannten Materialien enthält. Derartige Polymerfolien sind als coextrudierte Folien verfügbar, wobei die Dicke der Haftvermittlerschicht im Bereich von 3 bis 6 µm bei einer Gesamtdicke der Polymerfolie von 10 bis 40 µm liegt. Diese mehrschichtige Polymerfolie wird zum Aufbringen der Polymerbeschichtung mit der Haftvermittlerschicht zur Zinnoberfläche hin orientiert und so auf die oxidierte Zinnoberfläche auflaminiert. In Figur 3 ist ein entsprechend hergestelltes Weißblech im Schnitt dargestellt. Dieses umfasst die Schichten Stahlblech 1, Zinnbeschichtung 2, Zinnoxidschicht 3 und die auflaminierte Polymerbeschichtung mit der Haftvermittlerschicht 5 und der Polymerschicht 4 (bspw. aus PET).Suitable adhesion promoters are glycol modified polyethylene terephthalate (PETG wherein less than 50% of the diol component is cyclohexadimethanol), glycol modified polycyclohexylenedimethylene terephthalate (PCTG wherein more than 50% of the diol component is cyclohexadimethanol) and / or isophthalic acid (IPA). Coupling agents which have a proportion of PETG and 5 to 25% by volume of IPA or PCTG have proven to be particularly preferred. In order to form a bonding agent layer between the oxidized tin surface of the tinplate and the polymer coating, it is expedient to use a multilayered polymer film which contains a polymer layer (for example of PET) and an adhesion promoter layer of one of the abovementioned materials. Such polymer films are available as coextruded films, wherein the thickness of the adhesion promoter layer in the range of 3 to 6 microns with a total thickness of the polymer film from 10 to 40 microns. This multilayered polymer film is oriented toward the tin surface for application of the polymer coating with the adhesion promoter layer and is thus laminated onto the oxidized tin surface. In FIG. 3 a correspondingly manufactured tinplate is shown in section. This comprises the layers of steel sheet 1, tin coating 2, tin oxide layer 3 and the laminated polymer coating with the adhesion promoter layer 5 and the polymer layer 4 (for example made of PET).

Die erfindungsgemäß hergestellten Weißbleche eignen sich zur Herstellung von Verpackungsbehältern, insbesondere für Lebensmittel und für technische Füllgüter, wie z.B. zweiteilige Dosen (tiefgezogen und gestreckt, DWI-Dosen) und Aerosoldosen. Auch Dosenrümpfe von dreiteiligen Dosen kommen in Frage, wenn vor dem Rumpfschweißen die Polymerbeschichtung im Schweißbereich entfernt wird. Es können auch Teile solcher Verpackungsbehälter aus den erfindungsgemäß hergestellten Stahlbändern gefertigt werden, wie z.B. Laschenbänder, Ventilteller, Dosendeckel und Deckelringe. Daneben kann das erfindungsgemäße Verfahren auch für die Herstellung von Stahlblechen zur Anwendung in anderen Bereichen verwendet werden, wie z.B. für die Herstellung von Blechen für den Baubereich oder für die Herstellung von Haushaltsgeräten.The tinplates produced according to the invention are suitable for the production of packaging containers, in particular for foodstuffs and for technical filling goods, such as, for example, two-part cans (deep-drawn and stretched, DWI cans) and aerosol cans. Canned hulls of three-piece cans are also suitable if, before the hull welding Polymer coating is removed in the welding area. It is also possible to manufacture parts of such packaging containers from the steel strips produced according to the invention, such as flap bands, valve plates, can covers and cover rings. In addition, the inventive method can also be used for the production of steel sheets for use in other areas, such as for the production of sheets for the construction sector or for the production of household appliances.

Die Erfindung ist nicht auf die beschriebenen Ausführungsbeispiele beschränkt. So ist es bspw. im Rahmen der Erfindung möglich, das Stahlband 10 nach der elektrochemischen Oxidation der Zinnoberfläche auf eine Rolle (Coil) aufzuwickeln und es in dieser Form dem nächsten Verfahrensschritt (Aufbringen der Polymerbeschichtung) zuzuführen. Dies ist in der schematischen Darstellung der erfindungsgemäßen Vorrichtung der Figur 1 nicht berücksichtigt.The invention is not limited to the described embodiments. For example, within the scope of the invention, it is possible to wind the steel strip 10 onto a roll (coil) after the electrochemical oxidation of the tin surface and to feed it in this form to the next process step (application of the polymer coating). This is in the schematic representation of the device according to the invention FIG. 1 not considered.

Die Polymerbeschichtung kann auch durch andere Beschichtungsverfahren als Laminieren auf die Zinnbeschichtung aufgebracht werden. So kann nach dem elektrochemischen Oxidieren der Zinnoberfläche bspw. auch mittels Direktextrusion ein schmelzflüssiges Polymermaterial auf die oxidierte Zinnbeschichtung aufgebracht werden, wie es bspw. in der Patentschrift DE 197 30 893 C1 beschrieben ist.The polymer coating may also be applied to the tin coating by other than laminating methods. Thus, after the electrochemical oxidation of the tin surface, for example, by means of direct extrusion, a molten polymer material can be applied to the oxidized tin coating, as for example in the Patent DE 197 30 893 C1 is described.

Beim Aufbringen der Polymerbeschichtung sind auch Kombinationen unterschiedlicher Polymermaterialien möglich. So kann z. B. auf der Bandoberseite des verzinnten Stahlbands eine Polymerbeschichtung aus PET und auf der Bandunterseite eine Polymerbeschichtung aus PP aufgebracht werden. Dabei kann eine Polymerbeschichtung (PP oder PET) auch durch eine Lackierung ersetzt werden.When applying the polymer coating, combinations of different polymer materials are possible. So z. B. on the upper side of the tin-plated steel strip, a polymer coating of PET and on the underside of the belt, a polymer coating of PP are applied. In this case, a polymer coating (PP or PET) can also be replaced by a coating.

Claims (13)

  1. Method for coating of a chromium-free surface of a tin-plated steel sheet (1) with a polymer coating (4), wherein the chromium-free tin surface of the tin-plated steel sheet (1) is first electrochemically oxidized by anodic polarization of the tines steel sheet (1) in an aqueous and chromium-free electrolyte in a first step and a polymer coating (4) is applied on the oxidized tin surface in a second step, characterized in that the polymer coating (4) is applied by laminating a polymer film out of a polymer material or by direct extrusion of a molten polymer material, wherein the polymer material is polyethylene-terephthalate (PET) or polypropylene (PP) or polyethylene (PE).
  2. Method for the production of a tinplate coated with a polymer coating (4), with the following steps:
    - electrolytic deposition of a tin coating (2) on one or both sides of a steel sheet (1),
    - electrochemical oxidation of the surface of the tin coating (2),
    - application of a polymer coating on the oxidized surface of the tin coating with the method according to claim 1.
  3. Method according to Claim 2, characterized in that the electrochemical oxidation of the tin surface takes place immediately, preferably within a few seconds, after the deposition of the tin coating (2) on the steel sheet (1).
  4. Method according to one of the preceding claims, wherein the anodic polarization of the tinned steel sheet (1) in the aqueous and chromium-free electrolyte is performed at most as long as the charge density on the tin surface is at most 40 C/m2.
  5. Method according to one of the preceding claims, characterized in that the polymer coating (4) is applied by laminating a polymer film, in particular a coextruded plastic film with a polymer layer and an adhesion layer, on the chromium-free and oxidized tin surface of the steel sheet (1), wherein during the laminating on of the polymer coating (4), the steel sheet (1) is maintained at temperatures above the melting temperature (TSn) of the tin coating (2).
  6. Method according to Claim 1 or 2, characterized in that the polymer coating (4) is applied on the oxidized tin surface of the steel sheet (1) by laminating a biaxially oriented or amorphous cast-polyester film made of polyethylene- terephthalate (PET), on the oxidized tin surface of the steel sheet.
  7. Chromium-free passivated tinplate coated with a polymer coating (4) made of a polymer material, produced with the method according to one of claims 2 - 6, wherein between the tin surface of the tinplate and the polymer coating only a thin tin oxide layer (3) and optionally an adhesion promoter layer are present, wherein the tin oxide layer (3) is essentially made of tetravalent tin oxide (SnO2) and preferably has a thickness of at most 0.1 µm, and in particular less than 0.01 µm, characterized in that the polymer material is selected from the group comprising polyethylene-terephthalate (PET), polypropylene (PP) and polyethylene (PE).
  8. Tinplate according to Claim 7, characterized in that an adhesion promoter layer (5) is present between the tin oxide layer (3) and the polymer coating (4).
  9. Tinplate according to Claim 8, characterized in that the adhesion promoter layer (5) contains glycol-modified polyethylene-terephthalate (PETG), glycol-modified polycyclohexylenedimethylene terephthalate (PCTG), and/or isophthalic acid (IPA).
  10. Tinplate according to one of Claims 7 to 9, characterized in that an antiblock layer, which particularly is made of silicon oxide, is present on the upper side of the polymer coating (4) that is turned away from the tin-plated steel sheet (1).
  11. Tinplate according to one of Claims 7 to 10, characterized in that the tinplate is made from a cold-rolled steel band (10) from a low-carbon and unalloyed or low-alloy steel having a thickness of 0.05 to 0.50 mm by coating with a tin coating in a coating weight of 0.5 to 12 g/m2.
  12. Use of a tinplate coated with a polymer coating (4) according to one of Claims 7 to 10, for the production of packagings, in particular cans for food products and pet food, packagings for chemical-technical goods, aerosol cans, beverage cans, or parts for such packagings, in particular closures, lashing belts, valve plates, can lids or lid rings.
  13. Apparatus for performing the method according to one of Claims 1 to 6, comprising:
    - a transporting device (6) for continuous transport of a continuous steel band (10) in a transporting direction at a transporting speed, which is preferably greater than 200 m/min,
    - a tin-plating device (7) for galvanic coating of the steel strip moving through the coating device at the transporting speed with a tin coating(2),
    - an oxidation device (8) with an electrolysis bath (8a), in which an aqueous, chromium-free electrolyte is contained, through which the tin-plated steel band (10) is conducted at the strip speed, so as to electrochemically oxidize the tin surface, characterized in that the apparatus is also comprising
    a plastic coating device (9) for application of a polymer coating on one or both sides of the tin surface of the steel band (10) by laminating a polymer film out of a polymer material or by direct extrusion of a molten polymer material, and
    wherein the polymer material is selected from the group comprising polyethylene-terephthalate (PET), polypropylene (PP) and polyethylene (PE).
EP14171749.6A 2013-09-09 2014-06-10 Tinplate with a polymer coating and method for producing the same Active EP2845929B1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
RS20171217A RS56605B1 (en) 2013-09-09 2014-06-10 Tinplate with a polymer coating and method for producing the same
PL14171749T PL2845929T3 (en) 2013-09-09 2014-06-10 Tinplate with a polymer coating and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE102013109801.0A DE102013109801B4 (en) 2013-09-09 2013-09-09 Tinplate coated with a polymer coating and process for its production

Publications (2)

Publication Number Publication Date
EP2845929A1 EP2845929A1 (en) 2015-03-11
EP2845929B1 true EP2845929B1 (en) 2017-09-27

Family

ID=50884806

Family Applications (1)

Application Number Title Priority Date Filing Date
EP14171749.6A Active EP2845929B1 (en) 2013-09-09 2014-06-10 Tinplate with a polymer coating and method for producing the same

Country Status (12)

Country Link
US (1) US20150072167A1 (en)
EP (1) EP2845929B1 (en)
JP (1) JP6231447B2 (en)
CN (1) CN104415899B (en)
BR (1) BR102014018213B1 (en)
DE (1) DE102013109801B4 (en)
ES (1) ES2647519T3 (en)
NO (1) NO3033327T3 (en)
PL (1) PL2845929T3 (en)
PT (1) PT2845929T (en)
RS (1) RS56605B1 (en)
RU (1) RU2590546C2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE202020100524U1 (en) * 2020-01-31 2021-05-04 Thyssenkrupp Rasselstein Gmbh Sheet metal packaging product, in particular tinplate or electrolytically chrome-plated sheet steel
DE102020102382A1 (en) 2020-01-31 2021-08-05 Thyssenkrupp Rasselstein Gmbh Steel sheet with a surface profile with periodically recurring structural elements and a method for producing such a steel sheet
DE102020102381A1 (en) 2020-01-31 2021-08-05 Thyssenkrupp Rasselstein Gmbh Sheet metal packaging product, in particular tinplate or electrolytically chromium-plated sheet steel and method for producing a sheet metal packaging product

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT516956B1 (en) * 2015-06-29 2016-10-15 Andritz Ag Maschf DEVICE AND METHOD FOR PRODUCING A ZINCED STEEL STRIP
DE102015113878B4 (en) * 2015-08-21 2023-03-16 Thyssenkrupp Ag Process for the thermal treatment of a black plate coated with a conversion layer
DE102015217627B4 (en) 2015-09-15 2017-07-20 Thyssenkrupp Ag Belt processing device and method for processing a belt
DE102017108403B4 (en) * 2017-04-20 2021-05-06 Thyssenkrupp Ag Method for coating a steel strip
KR102176342B1 (en) * 2018-09-28 2020-11-09 주식회사 포스코 Method for manufacturing the electrical steel sheet product
BR112022012143A2 (en) * 2019-12-20 2022-08-30 Tata Steel Ijmuiden Bv METHOD FOR MANUFACTURING LAMINATED TIN PLATE, LAMINATED TIN PLATE PRODUCED IN THIS WAY AND USE THEREOF
US20230220579A1 (en) * 2020-03-13 2023-07-13 Tata Steel Ijmuiden B.V. Method for passivating a tinplate strip and apparatus for producing said passivated tinplate strip
US20210395851A1 (en) * 2020-06-17 2021-12-23 Axalta Coating Systems Ip Co., Llc Coated grain oriented electrical steel plates, and methods of producing the same

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB479681A (en) 1936-06-06 1938-02-07 Crosse & Blackwell Ltd An improved process for treating tinplate and tinplate articles
EP0312304A1 (en) 1987-10-15 1989-04-19 CMB Foodcan plc Laminated metal sheet
WO1997003823A1 (en) 1995-07-21 1997-02-06 British Steel Plc Polymer/metal laminate and method for producing the same
DE19730893C1 (en) 1997-05-02 1998-07-23 Rasselstein Hoesch Gmbh Coating metal band with plastic on one or both sides by direct extrusion
WO2012146654A1 (en) 2011-04-28 2012-11-01 Tata Steel Ijmuiden Bv Process for producing a polymer coated metal substrate and a metal strip substrate provided with a polymer coating
EP2802688A2 (en) 2012-01-12 2014-11-19 ThyssenKrupp Rasselstein GmbH Method for passivating tinplate

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE343641C (en) * 1916-08-31 1921-11-07 Henry Kingsford Harris Electrical switching device for display devices
JPS508691B1 (en) * 1970-03-11 1975-04-07
DE3436412A1 (en) 1984-10-04 1986-04-17 Toyo Kohan Co., Ltd., Tokio/Tokyo Process for the lamination of metal sheeting with polyester film
US5094924A (en) * 1988-10-19 1992-03-10 Kenzo Matsui Polyester resin film laminated steel sheet for drawn and ironed can
GB2242159B (en) * 1990-03-19 1994-02-02 Toyo Kohan Co Ltd Copolyester resin film-metal sheet laminates
US5234516A (en) * 1992-01-28 1993-08-10 Toyo Kohan Co., Ltd. Method for production of a polyethylene laminated metal sheet
CA2108728C (en) * 1993-10-19 2001-02-13 Takaaki Okamura Metal sheet laminated with triple layered thermoplastic resin and a method for producing thereof
EP0664209A1 (en) 1994-01-24 1995-07-26 TOYO KOHAN Co., Ltd Metal sheet laminated with resin films
DE10010758A1 (en) * 2000-03-04 2001-09-06 Henkel Kgaa Corrosion protection of zinc, aluminum and/or magnesium surfaces such as motor vehicle bodies, comprises passivation using complex fluorides of Ti, Zr, Hf, Si and/or B and organic polymers
JP2004074657A (en) * 2002-08-20 2004-03-11 Toyo Kohan Co Ltd Decorative film, decorative film molded product obtained by molding decorative film and decorative sheet obtained by laminating decorative film
ITTO20030027A1 (en) * 2003-01-21 2004-07-22 Europa Metalli Spa METHOD FOR FORMING A LAYER OF PASSIVATION ON AN ITEM PRESENTING AT LEAST A TINY SURFACE.
EP1599616B1 (en) * 2003-02-25 2012-04-11 Chemetall GmbH Method for coating metallic surfaces with a mixture containing at least two silanes
JP2005238718A (en) * 2004-02-27 2005-09-08 Nippon Steel Corp Laminated metal plate showing excellent smoothness for vessel and its manufacturing method
US20070172593A1 (en) 2004-08-09 2007-07-26 Sinsel John A Polymeric coating formulation and steel substrate composites
US8404357B2 (en) * 2007-08-23 2013-03-26 Nippon Steel & Sumitomo Metal Corporation Environmentally-friendly steel sheet for a can or a container as well as laminated and pre-coated steel sheet by using it
CN101269555A (en) * 2008-03-12 2008-09-24 上海人民塑料印刷厂 Metal can packing material and method of manufacturing the same
RS56562B1 (en) * 2012-07-02 2018-02-28 Tata Steel Ijmuiden Bv Method for producing tinplate and product produced therewith

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB479681A (en) 1936-06-06 1938-02-07 Crosse & Blackwell Ltd An improved process for treating tinplate and tinplate articles
EP0312304A1 (en) 1987-10-15 1989-04-19 CMB Foodcan plc Laminated metal sheet
WO1997003823A1 (en) 1995-07-21 1997-02-06 British Steel Plc Polymer/metal laminate and method for producing the same
DE19730893C1 (en) 1997-05-02 1998-07-23 Rasselstein Hoesch Gmbh Coating metal band with plastic on one or both sides by direct extrusion
WO2012146654A1 (en) 2011-04-28 2012-11-01 Tata Steel Ijmuiden Bv Process for producing a polymer coated metal substrate and a metal strip substrate provided with a polymer coating
EP2802688A2 (en) 2012-01-12 2014-11-19 ThyssenKrupp Rasselstein GmbH Method for passivating tinplate

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
"the technology of metal protection and decoration", 1998, article "Canmaking", pages: 127 - 128, XP055500626
MARINO XANTHOS: "Functional fillers for plastics", 2010, article "19.3 Antiblocking Fillers", pages: 395,401, XP055500628

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE202020100524U1 (en) * 2020-01-31 2021-05-04 Thyssenkrupp Rasselstein Gmbh Sheet metal packaging product, in particular tinplate or electrolytically chrome-plated sheet steel
DE102020102382A1 (en) 2020-01-31 2021-08-05 Thyssenkrupp Rasselstein Gmbh Steel sheet with a surface profile with periodically recurring structural elements and a method for producing such a steel sheet
DE102020102381A1 (en) 2020-01-31 2021-08-05 Thyssenkrupp Rasselstein Gmbh Sheet metal packaging product, in particular tinplate or electrolytically chromium-plated sheet steel and method for producing a sheet metal packaging product

Also Published As

Publication number Publication date
ES2647519T3 (en) 2017-12-22
BR102014018213B1 (en) 2021-12-21
EP2845929A1 (en) 2015-03-11
DE102013109801A1 (en) 2015-03-12
NO3033327T3 (en) 2018-06-02
BR102014018213A2 (en) 2015-09-29
US20150072167A1 (en) 2015-03-12
JP2015078427A (en) 2015-04-23
RS56605B1 (en) 2018-02-28
CN104415899A (en) 2015-03-18
DE102013109801B4 (en) 2020-07-09
RU2014135734A (en) 2016-03-27
CN104415899B (en) 2017-05-24
PT2845929T (en) 2017-12-15
RU2590546C2 (en) 2016-07-10
PL2845929T3 (en) 2018-04-30
JP6231447B2 (en) 2017-11-15

Similar Documents

Publication Publication Date Title
EP2845929B1 (en) Tinplate with a polymer coating and method for producing the same
EP2948302B1 (en) Method for producing galvanized fine or ultrafine sheet metal with high corrosion resistance
JP5467719B2 (en) Manufacturing method of surface-treated steel sheet
US9637826B2 (en) Steel sheet for containers and manufacturing method for same
DE69025579T2 (en) CONTAINER LID MADE OF LAYERED MATERIAL
DE3925141C2 (en) Process for the production of objects, in particular cans from surface-treated steel sheet
EP3133187B1 (en) Method for the thermal treatment of a black sheet coated with a conversion layer
EP1060032B1 (en) Coated metal strips
EP4118257B1 (en) Method for passivating a tinplate strip and apparatus for producing said passivated tinplate strip
DE69320854T2 (en) Laminated sheet steel for welded cans
DE4022361C2 (en) Tinned steel sheet with a chromium double layer and a copolyester resin laminate, process for its preparation and its use
JP2010255065A (en) Surface treated steel sheet and method of manufacturing the same
JP4872315B2 (en) Surface-treated steel sheet and method for producing the same, resin-coated steel sheet, can and can lid
US20230023925A1 (en) Method for manufacturing laminated tinplate, a laminated tinplate produced thereby and use thereof
JP2013127124A (en) Method for manufacturing surface treated steel sheet
JP5151964B2 (en) Surface-treated steel sheet, method for producing the same, and resin-coated steel sheet
JP5257192B2 (en) Method for producing surface-treated steel sheet and resin-coated steel sheet
DE4311481C2 (en) A metal sheet laminated with a double-layer thermoplastic resin
DE4232251A1 (en) Polyester laminated foil for food packaging - has improved stability to heat treatment
DE102018115668A1 (en) Coated metal sheet for the production of packaging containers and in particular can bodies for aerosol cans, and method for coating a metal sheet with a polymer coating
JP2012036424A (en) Method for manufacturing surface-treated steel sheet and method for manufacturing resin-covered steel sheet
JPH11140691A (en) Treatment of surface of steel sheet, surface-treated steel sheet and thermoplastic resin-coated steel sheet using surface-treated steel sheet

Legal Events

Date Code Title Description
17P Request for examination filed

Effective date: 20140610

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

R17P Request for examination filed (corrected)

Effective date: 20150911

RBV Designated contracting states (corrected)

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

17Q First examination report despatched

Effective date: 20151203

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20170614

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

Free format text: NOT ENGLISH

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

Ref country code: CH

Ref legal event code: NV

Representative=s name: LUCHS AND PARTNER AG PATENTANWAELTE, CH

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 932055

Country of ref document: AT

Kind code of ref document: T

Effective date: 20171015

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

Free format text: LANGUAGE OF EP DOCUMENT: GERMAN

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 502014005570

Country of ref document: DE

REG Reference to a national code

Ref country code: PT

Ref legal event code: SC4A

Ref document number: 2845929

Country of ref document: PT

Date of ref document: 20171215

Kind code of ref document: T

Free format text: AVAILABILITY OF NATIONAL TRANSLATION

Effective date: 20171206

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2647519

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20171222

REG Reference to a national code

Ref country code: NL

Ref legal event code: FP

REG Reference to a national code

Ref country code: NO

Ref legal event code: T2

Effective date: 20170927

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

REG Reference to a national code

Ref country code: SK

Ref legal event code: T3

Ref document number: E 26154

Country of ref document: SK

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

REG Reference to a national code

Ref country code: GR

Ref legal event code: EP

Ref document number: 20170403250

Country of ref document: GR

Effective date: 20180420

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180127

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 5

REG Reference to a national code

Ref country code: DE

Ref legal event code: R026

Ref document number: 502014005570

Country of ref document: DE

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

26 Opposition filed

Opponent name: TATA STEEL IJMUIDEN BV

Effective date: 20180627

PLAX Notice of opposition and request to file observation + time limit sent

Free format text: ORIGINAL CODE: EPIDOSNOBS2

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

PLBB Reply of patent proprietor to notice(s) of opposition received

Free format text: ORIGINAL CODE: EPIDOSNOBS3

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20180610

PLAB Opposition data, opponent's data or that of the opponent's representative modified

Free format text: ORIGINAL CODE: 0009299OPPO

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NO

Payment date: 20190620

Year of fee payment: 6

Ref country code: PT

Payment date: 20190530

Year of fee payment: 6

Ref country code: LU

Payment date: 20190619

Year of fee payment: 6

R26 Opposition filed (corrected)

Opponent name: TATA STEEL IJMUIDEN BV

Effective date: 20180627

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GR

Payment date: 20190619

Year of fee payment: 6

Ref country code: RS

Payment date: 20190603

Year of fee payment: 6

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: AT

Payment date: 20190618

Year of fee payment: 6

REG Reference to a national code

Ref country code: DE

Ref legal event code: R100

Ref document number: 502014005570

Country of ref document: DE

PLCK Communication despatched that opposition was rejected

Free format text: ORIGINAL CODE: EPIDOSNREJ1

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20140610

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

Ref country code: MK

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20170927

PLBN Opposition rejected

Free format text: ORIGINAL CODE: 0009273

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: OPPOSITION REJECTED

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170927

27O Opposition rejected

Effective date: 20200116

REG Reference to a national code

Ref country code: NO

Ref legal event code: MMEP

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201210

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: AT

Ref legal event code: MM01

Ref document number: 932055

Country of ref document: AT

Kind code of ref document: T

Effective date: 20200610

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RS

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200610

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200610

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210114

Ref country code: NO

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200630

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200630

Ref country code: GR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210111

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200630

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BG

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201231

Ref country code: AT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200610

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20200610

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20230719

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20240620

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20240619

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SK

Payment date: 20240530

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20240621

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: TR

Payment date: 20240530

Year of fee payment: 11

Ref country code: BE

Payment date: 20240618

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20240628

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20240808

Year of fee payment: 11