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AU3259699A - Laminated metal strip - Google Patents

Laminated metal strip Download PDF

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Publication number
AU3259699A
AU3259699A AU32596/99A AU3259699A AU3259699A AU 3259699 A AU3259699 A AU 3259699A AU 32596/99 A AU32596/99 A AU 32596/99A AU 3259699 A AU3259699 A AU 3259699A AU 3259699 A AU3259699 A AU 3259699A
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AU
Australia
Prior art keywords
metal strip
process according
chemical
thermoplastic resin
chemically
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.)
Granted
Application number
AU32596/99A
Other versions
AU741976B2 (en
Inventor
Brian John Bastable
Malcolm Robert Mallace
Ieuan Stephen Rees
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Corus UK Ltd
Original Assignee
British Steel PLC
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Filing date
Publication date
Application filed by British Steel PLC filed Critical British Steel PLC
Publication of AU3259699A publication Critical patent/AU3259699A/en
Application granted granted Critical
Publication of AU741976B2 publication Critical patent/AU741976B2/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/50Multilayers
    • B05D7/51One specific pretreatment, e.g. phosphatation, chromatation, in combination with one specific coating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D3/00Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
    • B05D3/10Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by other chemical means
    • B05D3/102Pretreatment of metallic substrates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/14Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to metal, e.g. car bodies

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Laminated Bodies (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)

Abstract

A process for producing laminated metal strip which comprises the steps of chemically treating the strip to form on at least one of its surfaces a non-metallic coating, and applying to that coated surface a coating of a thermoplastic resin to form a layer thereon. The first coating is preferably corrosion resistant and promotes adhesion with the thermoplastic resin. Preferably the non-metallic coating layer is a phosphate, chromate, oxalate, arsenate, a 2 component polymer, a combination of chromium, silicon and an organic active species, or silanes or azoles. Preferably the thermoplastic resin is polypropylene, polyethyleneterephthalate or a mixture thereof.

Description

WO 99/44756 PCT/GB99/00567 LAMINATED METAL STRIP This invention relates to laminated metal strip for use especially, but not exclusively, in the packaging industry and to methods of manufacturing such metal strip. More especially, the invention relates to a method of chemically treating metal strip prior to lamination with a thermoplastic material. Organic-coated metal substrates, for example thermoplastic resin coated tinplate or blackplate, are used, inter a//a, in the production of packaging materials, for example, food and beverage cans. As a result, organic coatings so used, are required to conform with strict performance criteria. To maintain the integrity of a can as well as to ensure that its contents are maintained in a suitable condition over a storage period which may span months or even longer, the coating must exhibit good stain resistance, corrosion resistance and resistance to delamination. Organic coatings have traditionally comprised solvent or water-based lacquers. Recently however, the use of laminated polymer films and coatings, such as thermoplastic resins, has been recognised as a viable alternative. In practice, organic coatings are not applied directly onto metal strip, such as mild steel or blackplate, because for packaging applications the metal surface is too reactive and underfilm corrosion can spread rapidly. Instead, the can-making industry uses metal/ic-coated mild steels, such as tinplate or electrolytically chromium-coated steel (ECCS) as substrates for WO 99/44756 PCT/GB99/00567 2 organic coatings. Currently, a surface-treated mild steel strip may comprise a chrome/CrO. or tin layer electrochemically deposited so that the final substrate has either a metallic chromium layer of typically from 50 to 150 mg/m 2 and a chromium oxide/hydroxide layer of typically from 10 to 30 mg/m 2 , or a layer of metallic tin of typically between 5 and 10 g/m 2 . In many applications it is preferred that tinplate is additionally subjected to chromate solution treatment, the amount of oxidisable chromium being between 1 and 10 mg/m 2 . Unfortunately, electro-plating pre-treatment is a costly and time consuming process. Not only are materials expensive, but the electro-plating process itself consumes large quantities of energy. In addition, this conventional pre-treatment adds an additional production step in the process line, which adds costs in terms of line-time, manpower and through yield. It has been shown that for some applications, the degree of protection afforded by the ECCS or tin pre-treatment exceeds the performance requirements of the can. For this reason and the disadvantages associated with electroplating discussed above, there is an increasing desire to develop an alternative metal strip pre-treatment which avoids these problems but maintains the performance requirements of certain classes of food, beverage or aerosol cans. Preferably, any such pre-treatment should be capable of application under the present day metal strip coating and lamination line conditions. In the past, there has been a general understanding in the industry that alternatives to electro-deposited. tin and/or chrome would afford significantly less substrate protection. However, if a suitable alternative pre treatment could be found, an electroplating process step would be unnecessary with consequent increases in yield, savings in energy and WO 99/44756 PCT/GB99/00567 3 reductions in the overall production costs of laminated metal strip. It is an object of the present invention to provide a suitable alternative to conventional electroplating of metal strip prior to coating with an organic resin, which provides adequate corrosion protection of the organically coated metal strip and provides and maintains good adhesion to such organic resin coatings. According to the present invention in one aspect, there is provided a process for producing laminated metal strip which comprises the steps of chemically treating the strip to form on at least one of its surfaces a non metallic coating, and applying to that coated surface a coating of a thermoplastic resin to form a layer thereon. The term "non-metallic coatings" as used herein refers to coatings which despite optionally including metal ions, differ from what is conventionally described as a metallic layer in that there is no native metal. Unlike a metal layer wherein metal atoms, through metallic bonding, solely form a crystalline structure, in the non-metallic coatings of the present invention, both metallic and non-metallic ions are distributed within an amorphous network. In another aspect, the invention provides a process for manufacturing laminated metal strip, the process comprising the steps of: (a) cleaning metal strip; (b) chemically pre-treating the cleaned metal strip to form on one or each of its surfaces a non-metallic chemical coating, which resists corrosion of the underlying metal substrate and promotes adhesion to a subsequently applied layer; and, (c) applying to the chemically-treated metal strip a coating of thermoplastic resin to form a protective layer on at least one surface thereof.
WO 99/44756 PCT/GB99/00567 4 The metal strip may be cold-rolled metal strip. Typically, the metal strip has a gauge of between 0.08 and 0.50mm. A preferred gauge is 0.18mm. In particular, it is preferred that the metal strip comprises mild steel (conventionally referred to as blackplate). Preferably, the metal strip is cleaned to remove all traces of contamination which may be present as a result of previous cold rolling and annealing processes. Typically, the metal strip is cleaned electrolytically using a caustic-based solution, although the nature of the cleaner does not influence the subsequent chemical treatment. After cleaning, the strip may be rinsed with water to remove all traces of the cleaning solution. The chemical coating may be applied to the metal strip using a conventional application method such as immersion, spraying, roller coating, or a combination thereof. Typically, the chemical coating is applied by immersing the cleaned metal strip in chemical contained in one or more treatment vessels. In one embodiment, the metal strip is chemically treated for less than 60 seconds; in other embodiments, the chemical treatment times are less than 30 seconds or less than 15 seconds. Preferably, the metal strip is chemically treated for less than 10 seconds; typically, 5 seconds. Typically, the metal strip is chemically treated at a temperature of less than 1000C, most preferably at less than 301C. In one aspect of the invention, the metal strip is chemically treated to form a chemical coating which prevents subsequent underfilm corrosion of the metal strip and promotes adhesion between the metal strip and WO 99/44756 PCT/GB99/00567 5 thermoplastic resin. The chemical coating may be referred to as a coupling agent since it forms a strong and durable chemical bridge at the interface between the metal substrate and the final organic resin coating. The chemical bridge has a dual role; it interacts with receptive inorganic surfaces to form tenacious chemical bonds at the interface with the metal substrate and at the interface with the organic resin coating. The chemical coating may comprise an oxyanion such as phosphate, chromate, oxalate or arsenate. Alternatively, or in addition, the coating may comprise yttrium, elements in the lanthanum series of the periodic table, silanes or azoles. When metal substrates are exposed to the atmosphere, the surface of the metal develops a naturally occurring surface oxide layer. Typically, the oxide layer on blackplate at ambient temperature will have an average thickness of between 2 and 20 mm. Thus, in one embodiment, the chemical coating may be applied to the metal oxide layer on the surface of the metal substrate. In one embodiment of the invention, the chemical coating comprises silanes. Silanes are a family of organosilicon monomers that are characterised by the formula R-SiX 3 , where R is an organofunctional group linked to silicon by a hydrolytically stable bond and X denotes hydrolyzable groups, such as alkoxy groups, which are converted to silanol groups on hydrolysis. Preferably, the chemical coating comprises CH 2
CH
2
CH
2 Si(OCH 3
)
3 , where R is a reactive functional group and X is the methoxy group. Without wishing to be bound by any theory, in order to react with the metal strip, the chemical coating may be converted to an active silanol by hydrolysis. In aqueous solution, the hydrolysed silane may react with the WO 99/44756 PCT/GB99/00567 6 inorganic surface hydroxyl groups on the metal oxide layer. In order to react with the organic resin layer, organic chemistry predicts the formation of chemical covalent bonds between the organofunctional group of the silane and the reactive species in the organic resin matrix. In addition, the formation of an interpenetrating polymer network of the silane and the organic polymer may involve the formation of a "diffused" polymer at the silane-polymer interface. Alternatively, the chemical treatment may comprise phosphates, for example zinc orthophosphates, manganese phosphates or iron phosphates, thereby producing crystalline phosphate coatings on the metal substrate. In a preferred embodiment of the invention the metal strip is chemically coated with a composition comprising less than 5% atomic chromium. In one embodiment, the chemical coating may comprise a commercially available chemical treatment comprising chromium, silicon and organic active species. Alternatively, the chemical coating may comprise a commercially available chemical treatment comprising a two component organic polymer i.e. an acrylic polymer and (NH 3 )Cr 2
O
6 . After chemical treatment, the metal strip may be rinsed and/or dried, for example with hot air, prior to treatment with organic resin. One or more layers of thermoplastic resin may be applied to one or both sides of the chemically-treated metal strip. The layer or layers of thermoplastic resin may be melted and rapidly quenched to attain the required degree of crystalline structure. Typically, a film of thermoplastic resin may be co-extruded with the WO 99/44756 PCT/GB99/00567 7 chemically-treated metal strip to form laminated metal strip. The film of thermoplastic resin may be bonded to chemically-treated metal strip under conditions of elevated temperature and pressure. The chemically-treated metal strip may be coated with a thermoplastic resin together with a bonding layer. The bonding layer may comprise a polyester, or an acid or acid-anhydride polyolefin resin containing carboxyl or anhydride groups. Typically, the bonding layer is between 1 and 10pm thick. Alternatively, the chemically-treated metal strip may be extrusion coated with at least one thermoplastic resin. Preferred thermoplastic resins comprise polypropylene (PP), polyethyleneteraphthalate (PET) or a combination thereof. Typically, the thickness of the layer, or layers, of thermoplastic resin are between 3 and 50pum. The chemical treatment has two functions; firstly it provides corrosion protection and inhibits underfilm corrosion, and secondly, it promotes good adhesion between the organic resin coating and the metal strip. These properties combined with the barrier properties of the organic coating provide a laminated metal strip product which can be formed into components for a range of applications whilst maintaining adequate performance criteria with regard to corrosion resistance and inter layer adhesion during the lifetime of the products. Therefore, in another aspect, the invention provides a laminated metal strip produced by a process which comprises the steps of chemically treating the strip to form on at least one of its surfaces a non-metallic coating, and applying to that coated surface a coating of a thermoplastic resin to form a WO 99/44756 PCT/GB99/00567 8 layer thereon. In another aspect, the invention provides a laminated metal strip produced by a process which comprises the steps of: (a) chemically pre-treating metal strip to form on one or each of its surfaces a non-metallic chemical coating, which resists corrosion of the underlying metal substrate and promotes adhesion to a subsequently applied layer; and, (b) applying to the chemically-treated metal strip a coating of thermoplastic resin to form a protective layer on at least one surface thereof. In yet another aspect, the invention provides a packaging container comprising such laminated metal strip. Chemical treatment obviates the need for a metallic coating on the metal strip substrate. As the conventional electroplated metal coating is normally applied on a separate process line to the organic coating line, the omission of this step results in considerable cost and energy savings, as well as increasing through yield. The invention will now be described by way of example only with reference to the accompanying diagrammatic drawings and tables in which: Figure 1 is a histogram showing the performance rating of food-filled cans made from PET-laminated and chemically treated blackplate; Figure 2 is a histogram showing the performance rating of food-filled cans made from PP-laminated and chemically treated blackplate; and, Table 1 tabulates the conditions, concentrations and dipping times of exemplary chemical treatments.
WO 99/44756 PCT/GB99/00567 9 A process line for producing laminated blackplate comprises a plurality of guide rollers for transporting a strip of blackplate continuously from a coiled roll to an exit coil via a multiplicity of vertical tanks. These tanks include a cleaning tank, rinsing tanks and a chemical treatment tank. The line speed is typically 10 to 100 metres per minute with a treatment dwell time of between 1 to 10 seconds. After hot-air drying, the chemically treated metal strip is laminated with organic polymeric resin e.g. a thermoplastic resin such as PET at elevated temperature and pressure. The laminated metal strip is then rapidly quenched to produce an essentially amorphous organic outer coating. By way of example, the performances of two commercially available chemical treatments (referred to below as chemicals A and B) were evaluated as potential alternatives to the conventional electroplating step in the production of an organically coated mild steel strip. Chemical A comprised a commercially available chemical treatment comprising chromium, silicon and organic active species. Chemical B comprised a commercially available chemical treatment comprising a two component organic polymer i.e. an acrylic polymer and (NH 3 )Cr 2 0 6 . In the evaluation, blackplate of 0.08 to 0.50mm thickness was subjected to an electrolytic cleaning process using a commercial cleaning solution at a temperature not exceeding 100 C, by passing a current of 20A for 5 seconds. This treatment is considered to return current densities to approximately 10 Adm 2 . The nature of the cleaner employed on the blackplate does not influence any subsequent chemical treatment. It is important that the metal strip is clean and free of contamination from prior processing. Before dipping in the chemical treatment vessels, the samples were washed in two ambient water rinse tanks. The concentrations of the cleaner and chemical treatments were those recommended by the respective suppliers. A batch of samples exposed only to electrolytic cleaning were WO 99/44756 PCT/GB99/00567 10 also prepared as a control sample group, identified in Figures 1 and 2 as B plate. As well as "cleaned only" samples, an ECCS control sample group was also laminated. Samples of both 15 pm PET and/or 40 pm PP were laminated at elevated temperature and pressure. The hot samples were plunged into cold water just as the current was switched off. Instant quenching of this nature has the effect of retaining the amorphous nature of the thermoplastic coating at ambient temperature. Table 1 illustrates the concentrations, dip times and treatment section temperatures for evaluated chemicals A and B. Samples of each variable were subjected to a wedge bend test. Both treatments A and B performed equally well; no delamination or cracking of the polymer was observed. A standard Erichsen and cross scored Erichsen were also performed. The samples were evaluated for signs of blisters and/or delamination. Again, both A and B performed well with little to distinguish between them. About 350, 73mm diameter classic can ends were produced on a conventional MB20 can end press. Approximately 20 samples of each treatment with both PET and PP were produced. A standard lining compound was applied to each end. Half the ends were lightly scored prior to filling with foodstuff to create a standard defect and potentially allow a greater degree of differentiation of the chemical treatments on opening. Soz cans (73 x 63mm) were filled with either rabbit cat food or cut green beans in salt brine under standard filling conditions. The cans were stored on their sides at an elevated temperature (371C). Cans with scored ends were stored with the score running vertically so that it entered the head space area. Four cans of each variable were opened after 2, 5, and 15 weeks. Opened cans were evaluated for sulphide staining, delamination and WO 99/44756 PCT/GB99/00567 11 corrosion (on and off the score line). The can end performance was judged on three main criteria (sulphide staining, delamination and corrosion (on and off the score line)) using a points system. Three points were awarded if the defect was obviously present and two points if the defect was only minor. No points were allocated if the defect was absent. All points were totalled for each category of defect over the three openings, for both polymer film types and for each chemical pre-treatment. The results are illustrated in Figure 1 and Figure 2. It should be noted that the performance rating system used here gives equal weighting to each of the attributable defects. Arguably, sulphide staining could be regarded as a less serious defect than delamination as it is only aesthetic and does not directly reflect can performance. Nevertheless, the approach highlights the chemical treatments which perform relatively adequately for use in can-making applications. In summary, the trials show that chemical pre-treatment in accordance with the invention provides an effective alternative to metallic electroplated coatings prior to coating of metal strip with organic resins. It may be envisaged that in another embodiment of the invention, blackplate can undergo chemical pre-treatment "off-line" with transfer to the lamination line post treatment. However, this is less cost effective due to the necessity for a separate coating facility and any associated transportation or storage costs. It will be appreciated that the foregoing is merely exemplary of treatments in accordance with the invention and that modifications can readily be made thereto without departing from the true scope of the invention.
WO 99/44756 PCT/GB99/00567 12 TABLE 1 Chemical Working Dip time Temperature of Treatment concentration (seconds) dip IC A 3% 1 25 B as supplied 3 <30

Claims (35)

1. A process for producing laminated metal strip which comprises the steps of chemically treating the strip to form on at least one of its surfaces a non-metallic coating, and applying to that coated surface a.coating of a thermoplastic resin to form a layer thereon.
2. A process for manufacturing laminated metal strip, the process comprising the steps of, (a) cleaning metal strip; (b) chemically pre-treating the cleaned metal strip to form on one or each of its surfaces a non-metallic chemical coating, which resists corrosion of the underlying metal substrate and promotes adhesion to a subsequently applied layer; and, (c) applying to the chemically-treated metal strip a coating of thermoplastic resin to form a protective layer on at least one surface thereof.
3. A process according to claim 1 or claim 2 wherein the metal strip is cold-rolled metal strip.
4. A process according to any one of the preceding claims wherein the metal strip has a gauge of between 0.08 and 0.50mm.
5. A process according to claim 4 wherein the metal strip has a gauge of 0.18mm.
6. A process according any one of the preceding claims wherein the metal strip comprises blackplate.
7. A process according to any one of the preceding claims wherein the metal strip is cleaned electrolytically. WO 99/44756 PCT/GB99/00567 14
8. A process according to any one of the preceding claims wherein the chemical coating is applied to the metal strip by a method of immersion, spraying, roller coating, or a combination thereof.
9. A process according to claim 8 wherein the chemical coating is applied by immersing the metal strip into at least one chemical treatment vessel.
10. A process according to claim 9 wherein the residence time of the metal strip in the chemical-treatment vessel is less than 60 seconds.
11. A process according to claim 10 wherein the residence time of the metal strip in the chemical-treatment vessel is less than 30 seconds.
12. A process according to claim 11 wherein the residence time of the metal strip in the chemical-treatment vessel is less than 15 seconds.
13. A process according to claim 12 wherein the residence time of the metal strip in the chemical-treatment vessel is less than 10 seconds, for example, 5 seconds.
14. A process according to any one of the preceding claims wherein the metal strip is chemically treated at a temperature of less than 1000 C, for example less than 300C.
15. A process according to any one of the preceding claims wherein the metal strip is chemically treated to form an anti-corrosive, adhesion promoting chemical coating between the metal strip and thermoplastic resin.
16. A process according to any one of the preceding claims wherein the chemical coating comprises an oxyanion such as phosphate, WO 99/44756 PCT/GB99/00567 15 chromate, oxalate or arsenate.
17. A process according to claim 16 wherein the chemical coating comprises a two component organic polymer.
18. A. process according to claim 16 wherein the chemical coating comprises chromium, silicon and an organic active species.
19. A process according to any one of the preceding claims wherein the chemical coating comprises yttrium, elements in the lanthanum series of the periodic table, silanes or azoles.
20. A process according to claim 19 wherein the chemical coating comprises silanes of the general formula, R-SiX 3 , where R is an organofunctional group linked to silicon by a hydrolytically stable bond and X denotes hydrolyzable groups, e.g. alkoxy groups, which are converted to silanol groups on hydrolysis.
21. A process according to claim 20 wherein the chemical coating comprises a silane of the general formula, RCH 2 CH 2 CH 2 Si(OCH 3 ) 3 , where R is a reactive functional group and X is the methoxy group.
22. A process according to claim 16 wherein the chemical coating comprises a phosphate such as zinc orthophosphates, manganese phosphates or iron phosphates.
23. A process according to any one of the preceding claims wherein the chemical coating comprises less than 5 atomic % chromium.
24. A process according to any one of the preceding claims wherein the WO 99/44756 PCT/GB99/00567 16 chemically-treated metal strip is rinsed and/or dried prior to organic resin coating.
25. A process according to any one of the preceding claims wherein one or more layers of thermoplastic resin are applied to one or both sides of the chemically-treated metal strip.
26. A process according to any one of the preceding claims wherein the layer or layers of thermoplastic resin is/are melted and rapidly quenched to attain the required degree of crystalline structure.
27. A process according to any one of the preceding claims wherein the chemically-treated metal strip is extrusion coated with at least one thermoplastic resin.
28. A process according to claim 27 wherein the film of thermoplastic resin is bonded to the chemically-treated metal strip under conditions of elevated temperature and pressure.
29. A process according to any one of the preceding claims wherein the chemically-treated metal strip is coated with thermoplastic resin together with a bonding layer.
30. A process according to claim 29 wherein the bonding layer comprises a polyester or an acid or acid-anhydride polyolefin resin containing carboxyl or anhydride groups.
31. A process according to claim 29 or claim 30 wherein the thickness of the bonding layer is between 1 and 10 pm.
32. A process according to any one of the preceding claims wherein the thermoplastic resin comprises polypropylene (PP), WO 99/44756 PCT/GB99/00567 17 polyethyleneterephthalate (PET) or a combination thereof.
33. A process according to any one of the preceding claims wherein the thickness of the layer, or layers, of thermoplastic resin is/are between 3 and 50 pm.
34. A process as substantially defined herein and with reference to the accompanying Figures and Table.
35. A laminated metal strip as manufactured by the process as defined in claim 34.
AU32596/99A 1998-03-02 1999-03-02 Laminated metal strip Ceased AU741976B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB9804297 1998-03-02
GB9804297A GB2334906A (en) 1998-03-02 1998-03-02 Laminated metal strip
PCT/GB1999/000567 WO1999044756A2 (en) 1998-03-02 1999-03-02 Coated metal strips

Publications (2)

Publication Number Publication Date
AU3259699A true AU3259699A (en) 1999-09-20
AU741976B2 AU741976B2 (en) 2001-12-13

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EP (1) EP1060032B1 (en)
KR (1) KR20010041481A (en)
CN (1) CN1291918A (en)
AT (1) ATE218930T1 (en)
AU (1) AU741976B2 (en)
BR (1) BR9908396A (en)
CA (1) CA2322533A1 (en)
DE (1) DE69901797T2 (en)
ES (1) ES2178453T3 (en)
GB (1) GB2334906A (en)
ID (1) ID28089A (en)
PL (1) PL343020A1 (en)
RU (2) RU2220789C2 (en)
WO (1) WO1999044756A2 (en)

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PL343020A1 (en) 2001-07-30
RU2220789C2 (en) 2004-01-10
DE69901797T2 (en) 2003-03-06
RU2003124575A (en) 2005-02-27
EP1060032A2 (en) 2000-12-20
ES2178453T3 (en) 2002-12-16
CN1291918A (en) 2001-04-18
DE69901797D1 (en) 2002-07-18
BR9908396A (en) 2000-10-31
CA2322533A1 (en) 1999-09-10
GB2334906A (en) 1999-09-08
AU741976B2 (en) 2001-12-13
KR20010041481A (en) 2001-05-25
ATE218930T1 (en) 2002-06-15
EP1060032B1 (en) 2002-06-12
GB9804297D0 (en) 1998-04-22
WO1999044756A3 (en) 1999-11-25
ID28089A (en) 2001-05-03
WO1999044756A2 (en) 1999-09-10

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