GB2053285A - Treatment of metal surfaces - Google Patents
Treatment of metal surfaces Download PDFInfo
- Publication number
- GB2053285A GB2053285A GB8016966A GB8016966A GB2053285A GB 2053285 A GB2053285 A GB 2053285A GB 8016966 A GB8016966 A GB 8016966A GB 8016966 A GB8016966 A GB 8016966A GB 2053285 A GB2053285 A GB 2053285A
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- GB
- United Kingdom
- Prior art keywords
- zirconium
- solution
- tinplate
- staining
- sulphide
- 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
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- 229910052751 metal Inorganic materials 0.000 title claims abstract description 13
- 239000002184 metal Substances 0.000 title claims abstract description 13
- 238000011282 treatment Methods 0.000 title description 14
- 239000005028 tinplate Substances 0.000 claims abstract description 25
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims abstract description 22
- 150000003755 zirconium compounds Chemical class 0.000 claims abstract description 12
- DUFCMRCMPHIFTR-UHFFFAOYSA-N 5-(dimethylsulfamoyl)-2-methylfuran-3-carboxylic acid Chemical compound CN(C)S(=O)(=O)C1=CC(C(O)=O)=C(C)O1 DUFCMRCMPHIFTR-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910017053 inorganic salt Inorganic materials 0.000 claims abstract description 4
- WRAGBEWQGHCDDU-UHFFFAOYSA-M C([O-])([O-])=O.[NH4+].[Zr+] Chemical compound C([O-])([O-])=O.[NH4+].[Zr+] WRAGBEWQGHCDDU-UHFFFAOYSA-M 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 23
- 238000010186 staining Methods 0.000 claims description 23
- 239000002904 solvent Substances 0.000 claims description 10
- 238000004140 cleaning Methods 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 5
- 238000009736 wetting Methods 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 3
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims 1
- 238000000576 coating method Methods 0.000 abstract description 5
- 239000011248 coating agent Substances 0.000 abstract description 3
- 235000013324 preserved food Nutrition 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 26
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 9
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 9
- 229910052726 zirconium Inorganic materials 0.000 description 8
- 235000013305 food Nutrition 0.000 description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 239000005864 Sulphur Substances 0.000 description 5
- 238000002161 passivation Methods 0.000 description 5
- MBMLMWLHJBBADN-UHFFFAOYSA-N Ferrous sulfide Chemical group [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 description 4
- 238000007739 conversion coating Methods 0.000 description 4
- 238000007654 immersion Methods 0.000 description 4
- 229910052911 sodium silicate Inorganic materials 0.000 description 4
- 231100000331 toxic Toxicity 0.000 description 4
- 230000002588 toxic effect Effects 0.000 description 4
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 4
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 4
- 235000019801 trisodium phosphate Nutrition 0.000 description 4
- -1 Na3PO4 or a silicate Chemical compound 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 239000004922 lacquer Substances 0.000 description 3
- 235000019795 sodium metasilicate Nutrition 0.000 description 3
- 229910001887 tin oxide Inorganic materials 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 2
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 229910052976 metal sulfide Inorganic materials 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- AFNRRBXCCXDRPS-UHFFFAOYSA-N tin(ii) sulfide Chemical compound [Sn]=S AFNRRBXCCXDRPS-UHFFFAOYSA-N 0.000 description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 239000007836 KH2PO4 Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- JHGFRCLDPHKRBS-UHFFFAOYSA-N [Sn+2]=O.[O-2].[Zr+4].[O-2].[O-2] Chemical group [Sn+2]=O.[O-2].[Zr+4].[O-2].[O-2] JHGFRCLDPHKRBS-UHFFFAOYSA-N 0.000 description 1
- 229910000318 alkali metal phosphate Inorganic materials 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 150000001845 chromium compounds Chemical class 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000002659 electrodeposit Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000004673 fluoride salts Chemical class 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- NNIPDXPTJYIMKW-UHFFFAOYSA-N iron tin Chemical compound [Fe].[Sn] NNIPDXPTJYIMKW-UHFFFAOYSA-N 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical class [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/73—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals characterised by the process
- C23C22/74—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals characterised by the process for obtaining burned-in conversion coatings
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Chemical Treatment Of Metals (AREA)
Abstract
A metal surface, particularly a tinplate can for canned food, is treated by contact with a solution containing a zirconium compound, particularly ammonium zirconium carbonate or zirconium acetate. An inorganic salt may also be present in the solution. The concentration of the zirconium compound, calculated as ZrO2, is between 0.1 and 10% w/w. The surface is thereafter heated to a temperature between 20 and 300 DEG C until it is dry. The surface may be cleaned prior to contact with the solution. In this way a coating is provided on the surface which improves the stain resistance of the surface.
Description
SPECIFICATION
Treatment of metal surfaces
This invention relates to a method of treating a metal surface, particularly so as to protect the
surface from sulphide staining. The invention also includes within its scope a surface which has been so treated and an article, particularly a can, having such a surface.
Untreated tinplate develops a dark irregular stain when in contact with a range of sulphur-bearing natural products under the conditions used in food processing. Sulphur-bearing proteins are present in many foods which are preserved in cans, and after processing the interior surface of the can is often discoloured to a marked degree due to the formation of metal sulphides, while the food in contact with such discoloured areas may itself become stained. The stain appears to be harmless, but is objectionable and should be avoided.
It is common practice to improve corrosion and stain resistance characteristics and paint bonding qualities of a metal surface by depositing on it a protective coating, known as a conversion coating, for example the treatment known as passivation in the tinplate industry. It is also known to subsequently treat the surface having the conversion coating to improve the qualities of the coating.
Conventionally the conversion coating for a variety of metals consists of a solution of phosphoric acid containing zinc oxide, chromic acid or soluble fluorides, depending upon the metal to be treated.
Subsequent rinsing treatment usually consists of chromic acid and a soluble fluoride.
In view of the toxic nature of chromium VI compounds, it would be preferable to use an alternative, non-toxic material to produce a stain-resistant finish to tinplate. This is particularly important in the treatment of drawn plain containers.
Tin sulphide staining generally occurs where the tinplate surface is unprotected by a passivation film of the 'cathodic dichromate' type. It takes the form of uneven discolouration of the surface and is expected on unlacquered two-piece containers because the passivation films are destroyed by the forming operations. Iron sulphide forms where the tinplate steel base is exposed in the headspace above a sulphur-bearing food product. The stains are black and can become detached from the tinplate.
Unlacquered two-piece cans are highly susceptible to iron sulphide staining because the tin coating applied by the tin-plate manufacturers is severely disrupted during the forming operation. Generally, where a product is believed to give rise to iron sulphide staining, lacquers are used to prevent the unsightly black stain forming.
It has been found that zirconium componds are useful as components in conversion coating systems, which provide metal surfaces with some corrosion protection. The use of zirconium-containing materials, generally in conjunction with conventional phosphating processes is described in, for example, British Patent Specification 1,479,638. Some of the treatments described, it is claimed, improve the adhesion to subsequently applied lacquers.
It has also been proposed in British Patent Specifications 479,681 and 479,746 to prevent sulphide-staining of tinplate by anodic polarisation in dilute ammonia, ammonium carbonate or alkali metal phosphates. It is suggested that this treatment produces a stable tin oxide film that prevents the formation of metal sulphides during processing of food.
The most effective of the above-mentioned treatments involves the use of the toxic chromium Vl compounds. The object of the present invention is to obviate the need for toxic chromium compounds whilst providing an equally or more effective treatment method.
According to the invention, a method of treating a metal surface comprises the steps: contacting said surface with a solution free of organic polymeric materials and comprising a solvent and a zirconium compound at a concentration, calculated as ZrO2, in the range between 0.1 and 10% w/w; and thereafter heating said surface to a temperature in the range between 20 and 300 C until said surface is dry, said surface being capable of wetting by said solvent.
The solution may further comprise an inorganic salt, such as a phosphate, particularly Na3PO4 or a silicate, particularly Na2SiO3, or a borate.
The zirconium compound is preferably ammonium zirconium carbonate (hereinafter referred to as AZC), or zirconium acetate, and is preferably at a concentration, calculated as Zero2, in the range between 0.2 and 2% w/w. The surface is preferably tinplate and the solvent is preferably water.
The method may comprise the further step of cleaning said surface, so as to make it capable of wetting by said solvent, prior to said contacting step. The cleaning step may comprise passing a current between said surface and an auxiliary electrode in said solution.
The invention will now be described by way of example only in the following examples. Two AZC solutions were obtained from a major UK supplier, Magnesium Elektron; one simply AZC, and the other a stabilised form Bacote 20 containing traces of tartrate and citrate. Both solutions contain 20% w/w Zero2. Most of the subsequent work involved Bacote 20.
After treatment in the solutions containing the zirconium compounds, the samples underwent a sulphide-staining test. They were placed in a dried pea and brine staining medium and heated to 121 0C in a pressure cooker for one hour. The degree of staining was assessed visually. Some samples were examined in a scanning electron microscope using an X-ray analyser.
EXAMPLE 1
To establish the conditions under which a sulphide stain-resistant finish can be produced on drawn tinplate using AZC, the following experiments were made.
Unwashed, drawn and wall-ironed (DWI) can sections were solvent cleaned by immersion in butyl cellosolve, followed by washing in hot ( > 900C) 25% Decon 90 solution and a distilled water rinse. The sections were then immersed in stablised AZC solutions (0.002 to 20%w/w ZrO2) for a few seconds. The specimens were dried in an oven at 1 000C. Similarly cleaned sections were briefly immersed in a dilute AZC solution (0.5% w/w ZrO2) and dried at temperatures ranging from 20 to 3000C.
The effectiveness of each treatment was assessed by subjecting the sample to the sulphidestaining test mentioned above. The results are shown in Table 1.
TABLE 1
SULPHIDE STAINING OF AZC TREATED DWI CAN SECTIONS
Concentration of AZC Oven
Temperature Sulphide
As Bacote 20 (bRo) As ZrO2 (%) ( C) Stain*
100 20 100 3-4
50 10 100 3-4
10 2 100 1
5 1 100 1
2.5 0.5 100 1
1 0.2 100 2-3
0.5 0.1 100 - 3-4
0.1 0.02 100 4-5
0.01 0.002 100 4-5
2.5 0.5 20 2
2.5 0.5 50 1
2.5 0.5 150 1-2
2.5 0.5 200 1-2
2.5 0.5 250 1-2
2.5 0.5 300 1-2
Untreated DWI samples 5
* Staining 1 None 3 Borderline acceptability
2 Slight 5 Severe (as received samples)
It is thus apparent that adequate sulphide stain resistance can be achieved by briefly immersing clean tinplate in an AZC solution of ZrO2 content between 0.1 and 10% and drying at temperatures between 20 and 3000C. The ZrO2 content is preferably between 0.2 and 2% w/w.
The results indicate that a protective film was produced on the clean surface when a dilute AZC solution was dried on the drawn tinplate. The film once formed was not destroyed by rinsing the can in water and-redrying. The stain resistance did not arise either when undiluted AZC was dried or when the dilute AZC was not dried before staining. Of the specimens examined in the scanning electron microscope after staining, only those that did not stain had detectable zirconium on the surface.
The interaction that produces stain resistance occurs during the decomposition of the dilute AZC solution on the metal surface. A possible explanation of this effect may lie in the strong affinity of zirconium for oxygen. The decomposition of the AZC complex may allow the zirconium to attach to the tin oxides on the surface.
This bonding is likely to be strong and the complex zirconium oxide - tin oxide structure sufficiently stable to prevent sulphide ions reacting with the tin oxide during processing.
Zirconium was detected on the surface of stain-resistant, treated samples. It is most likely that it would be present as an oxide as it is not possible to electrodeposit zirconium metal from aqueous solutIons.
EXAMPLE 2
Table 2 shows the results obtained when as received (uncleaned) sections cut from 211 x 400 plain tinplate cans, drawn and redrawn (DRD) using a lubricant, were treated in Bacote 20 and dilute
Bacote 20 (1% Zoo2). Only the cathodically polarised specimen, subsequently rinsed in dilute Bacote 20' and dried before staining, had an adequate stain resistance.
TABLE 2
SULPHUR STAIN RESISTANCE OF DRD CAN SECTIONS TREATED
IN AZC (BACOTE 20)
Treated In Sulphur
Specimen Bacote 20 Rinse Drying Stain
B None - 5
1 Immersion Dilute B20 Oven 4-5
2 Cathodic Dilute B20 Oven 2
3 None Dilute B20 Oven 5
* See Table 1.
It is therefore apparent that sulphide stain resistance can be conferred to drawn tinplate when a dilute AZC solution dries on a clean surface. If the sample is not cleaned before immersion in AZC, the cathodic polarisation is required to allow adequate wetting of the metal surface. The current does not produce the surface active species, but merely cleans the surface of any corrosion-resistant (oil) coatings which have been applied, for example by the manufacturer, or of any lubricants which have been applied to the surface, e.g. in can-drawing. This electrolytic cleaning need not be carried out separately in an undiluted Bacote 20 solution, but could be carried out in sltu in the dilute Bacote 20 solution, thus obviating the need for a separate cleaning step.If the cleaning step is to be carried out separately, then other cleaning means, e.g. solvents could be used.
EXAMPLE 3
A DWI can section, cleaned as described in Example 1, was immersed in a solution of zirconium acetate at a concentration (calculated as ZrO2) of 0.5% w/w and then dried in an oven at 1 000C. The sample was then subjected to the suiphide-staining test and showed a resultant staining (referring to the scale in TABLE 1) of 2.
EXAMPLE 4
Conventionally, tinplate when received from the manufacturers has already been subjected to a passivation treatment, and in the previous Examples such passivated tinplate was used, the drawing processes described in those Examples destroying the effectiveness of any coatings on the tinplate.
In this Example unpassivated undrawn electrolytic tinplate was solvent-cleaned, as described in
Example 1, then immersed in an AZC solution (0.5% w/w ZrO2), and then dried in an oven at 1 000C.
When subjected to the sulphide-staining test, this sample showed a staining of 1 (referring again to the scale in Table 1). A control, being as received unpassivated undrawn tinplate, which was not treated with AZC, when subjected to the same test showed a staining of 5.
EXAMPLE 5
211 x 400 DRD (drawn and redrawn) cans were cleaned internally by cathodic treatment in 5 gIl solution of Na2CO3, washed in distilled water and filled with the zirconium-containing solution. This solution was allowed to contact the whole can wall briefly before being poured out and reused. The cans were dried in an oven at 1200 C.
The results are shown in the Table 3 below.
TABLE 3
Degree of Sulphide Solution Composition Staining ZrO2 content % Inorganic % Tin Iron 2 Na3PO4 1.5 1 2 2 Na3PO4 1 1 1 2 Na2SiO, 1 1 2 2 Na2SiO3 0.75 2 2 1 Na2SiO3 0.75 1 1 2 ~ 1 4 2 NaBO 1 2 3 2 K2B4O, 1 23 1-2 2 NaH2PO4 1 2 4 2 KH2PO4 1 2 4 2 NH4H2PO4 1 1-2 4 *) Degree of sulphide staining.
1 Negligible 4 Moderate
2 Slight 5 Severe
3 Borderline acceptability
The above results indicate that additions of inorganic salts, particularly sodium silicate or trisodium phosphate can improve the iron sulphide staining resistance of drawn tinplate without seriously impairing the tin sulphide stain performance.
Although in the above Examples, reference has been made to immersion of the surface in the solution containing a zirconium compound, it will be apparent that any other means, for example spraying, of contacting the surface with the solution are equally feasible.
Summarising, zirconium compounds, particularly AZC and zirconium acetate, are capable of giving acceptable sulphide stain resistance to clean tinplate. The mechanism is not electrolytic and the only requirement is that a dilute AZC solution should dry in contact with the surface. The addition to the zirconium-containing solution of inorganic salts is also shown to be advantageous.
An immediate application for the invention might be in the treatment of DWI food cans, as either a replacement for chromate in the washer or preferably in place of the oil in the bodymaker. The latter course, if feasible, would reduce the size of the washer required. DWI food cans, successfully treated with AZC or zirconium acetate, would not require internal spray lacquering for some applications, and the cost of the lacquer could be saved.
The use of zirconium compounds to replace chromates in tinplate strip passivation would remove the cost of electricity and the equipment needed to provide a current and that required to ensure removal of toxic materials from the rinse water.
The method of the present invention is thus advantageous both practically and economically.
Claims (18)
1. A method of treating a metal surface comprising the steps: contacting said surface with a solution free of organic polymeric materials and comprising a solvent and a zirconium compound at a concentration, calculated as ZrO2, in the range between 0.1 and 10% w/w; and thereafter heating said surface to a temperature in the range between 20 and 3000C until said surface is dry, said surface being capable of wetting by said solvent.
2. A method according to Claim 1, wherein said solution further comprises an inorganic salt.
3. A method according to Claim 1 or Claim 2, wherein said zirconium compound is ammonium zirconium carbonate.
4. A method according to Claim 1 or Claim 2, wherein said zirconium compound is zirconium acetate.
5. A method according to any one of the preceding claims, wherein the concentration of said zirconium compound, calculated as Zero2, is in the range between 0.2 and 2% w/w.
6. A method according to any one of the preceding claims, wherein said surface is of tinplate.
7. A method according to any one of the preceding claims, wherein said solvent is water.
8. A method according to Claim 2 or any one of Claims 3 to 7 when appendant to Claim 2, wherein said inorganic salt is a phosphate, a silicate or a borate.
9. A method according to any one of the preceding claims, further comprising cleaning said surface, so as to make it capable of wetting by said solvent, prior to said contacting step.
1 0. A method according to Claim 9, wherein said cleaning step comprises passing a current between said surface and an auxiliary electrode in said solution.
11. A method according to any one of the preceding claims, further comprising the subsequent steps of rinsing and re-drying said surface.
1 2. A method of treating a metal surface substantially as hereinbefore described in any one of the
Examples.
13. A method of protecting a surface from sulphide-staining, comprising a method according to any one of the preceding claims.
14. A method of protecting a surface from sulphide-staining substantially as hereinbefore described in any one of the Examples.
1 5. A surface which has been treated or protected by a method according to any one of the preceding claims.
1 6. A surface according to Claim 1 5, said surface being of tinplate.
1 7. An article having at least one surface according to Claim 1 5 or Claim 1 6.
18. A can being an article according to Claim 17.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8016966A GB2053285B (en) | 1979-06-07 | 1980-05-22 | Treatment of metal surfaces |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB7919793 | 1979-06-07 | ||
| GB8016966A GB2053285B (en) | 1979-06-07 | 1980-05-22 | Treatment of metal surfaces |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| GB2053285A true GB2053285A (en) | 1981-02-04 |
| GB2053285B GB2053285B (en) | 1984-05-02 |
Family
ID=26271779
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB8016966A Expired GB2053285B (en) | 1979-06-07 | 1980-05-22 | Treatment of metal surfaces |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB2053285B (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8168276B2 (en) | 2006-09-19 | 2012-05-01 | Valspar Sourcing, Inc. | Food and beverage containers and methods of coating |
| EP3473684A1 (en) * | 2006-09-19 | 2019-04-24 | Swimc Llc | Coating composition for food and beverage container |
-
1980
- 1980-05-22 GB GB8016966A patent/GB2053285B/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8168276B2 (en) | 2006-09-19 | 2012-05-01 | Valspar Sourcing, Inc. | Food and beverage containers and methods of coating |
| EP3473684A1 (en) * | 2006-09-19 | 2019-04-24 | Swimc Llc | Coating composition for food and beverage container |
| US10752400B2 (en) | 2006-09-19 | 2020-08-25 | Valspar Sourcing, Inc. | Food and beverage containers and methods of coating |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2053285B (en) | 1984-05-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PCNP | Patent ceased through non-payment of renewal fee |