EP0048270A4 - Zinc-aluminum coatings. - Google Patents

Zinc-aluminum coatings.

Info

Publication number
EP0048270A4
EP0048270A4 EP19810901054 EP81901054A EP0048270A4 EP 0048270 A4 EP0048270 A4 EP 0048270A4 EP 19810901054 EP19810901054 EP 19810901054 EP 81901054 A EP81901054 A EP 81901054A EP 0048270 A4 EP0048270 A4 EP 0048270A4
Authority
EP
European Patent Office
Prior art keywords
alloy
mischmetal
alloy according
zinc
metal
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
EP19810901054
Other languages
German (de)
French (fr)
Other versions
EP0048270A1 (en
EP0048270B1 (en
Inventor
Schrade F Radtke
Dimitri Coutsouradis
Jacques Pelerin
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.)
International Lead Zinc Research Organization Inc
Original Assignee
International Lead Zinc Research Organization Inc
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
Priority claimed from BE6/471152A external-priority patent/BE882431A/en
Application filed by International Lead Zinc Research Organization Inc filed Critical International Lead Zinc Research Organization Inc
Priority to AT81901054T priority Critical patent/ATE14900T1/en
Publication of EP0048270A1 publication Critical patent/EP0048270A1/en
Publication of EP0048270A4 publication Critical patent/EP0048270A4/en
Application granted granted Critical
Publication of EP0048270B1 publication Critical patent/EP0048270B1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C18/00Alloys based on zinc
    • C22C18/04Alloys based on zinc with aluminium as the next major constituent
    • 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/04Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
    • C23C2/06Zinc or cadmium or alloys based thereon

Definitions

  • the present invention is directed to the appli- cation of zinc coatings to a substrate - commonly sheet steel.
  • hot dip galva ⁇ nizing either continuous or batch type, has long been used for a variety of steel products to protect the products from corrosion.
  • 3,343,930 and 3,393,089) reportedly exhibits a good corrosion resistance but, in view of its high aluminum content does not provide a satis ⁇ factory sacrificial protection of the steel substrate, Subsequent-s-fcudies have been aimed at modifying the composition of molten metal baths in order to form (by hot-dipping) a coating which improves corrosion resistance even in the most varied environ ⁇ ments.
  • One of the aspects of these studies was the influence of the preparation of the surface to be coated on the quality of the product obtained. It thus appears that in order to ensure a quality coating, some of the alloy coatings previously developed required expensive preliminary surface treatments involving expensive equipment.
  • the bath compositions and resultant coatings constitute improvements over known alloy " batha.-and coatings in that they contain additionally mixtures of rare earth elements.
  • the present invention is directed to zinc-aluminu ⁇ compositions or alloys which have added thereto rare earths in the form of mischmetal.
  • the zinc-aluminum alloys be what are commonly referred to as low aluminum zinc alloys which are generally recognized to contain from about 3% to about 15% aluminum.
  • the hot-dip metal baths according to the present invention may vary considerably just as known zinc-aluminum baths and coatings may vary. In each instance, however, it is essential that the bath have added thereto a mischmetal alloy in an amount sufficient to yield the improved results observed and described herein.
  • mischmetal refers to a variety of knovm rare earth alloys.
  • two typical cerium mischmetals might have the following compositions (in weight %) :
  • Ce 45-60 other rare earths 35-50, the balance comprising Fe, Mg, Al, Si and impurities.
  • Typical Lanthanum mischmetals can be defined by the following (in weight %) :
  • mischmetal refers to the above compositions as well as other mischmetal compositions readily apparent to those skilled in the art.
  • the preferred alloy to which mischmetal is to be added is a zinc-aluminum alloy containing from about 3% to about 15% aluminum. Such alloys typically contain about 5% aluminum. These alloys may contain constituents in addition to mischmetal such as Fe, Pb, Sb, Mg, Sn, Cu and Si.
  • one embodiment of the invention comprises a low aluminum (i.e., 3-15%) zinc bath containing Pb or Sn as well as mischmetal.
  • Pb and Sn are known additives to galvanizing baths for modifying the fluidity of the liquid metal or the spangle of the solidified coating.
  • Zinc-aluminum alloys containing lead and also Mg and Cu are reported to be immune to grain boundary corrosion.
  • mischmetal additions have been shown to exhibit a pronounced beneficial effect as regards soundness and uniformity.
  • a Zn-Al alloy containing Mg, Pb, Cu and misch- metal is encompassed by the present invention.
  • a typical composition might contain 3-15% Al, 0.02- 0.15% Mg, 0.02-0.15% Pb and possibly 0.1-0.3% Cu, the balance being Zn with mischmetal additions.
  • mischmetals may be advantageously used according to the invention, including mixtures of mischmetals in a single zinc bath or coating.
  • a La-mischmetal and a Ce-misch ⁇ ietal may be added simultaneously, preferably in an amount such that the total mischmetal concentration is within the ranges described above, i.e. from about 5 ppm to about 1.0% and preferably from about 0.01 to 0.1% by weight.
  • a master alloy may be first prepared and then added to the zinc bath so as to yield the desired mischmetal concentration.
  • Such master alloys might be comprised of 20% Zn and 80% mischmetal or 85-95% Al and 15-5% mischmetal.
  • EXAMPLES 1 Specimens of rimming steel sheet measuring 68 x 120 x 0.7 mm were galvanized in a device simulating a continuous galvanizing bath. They were first pre ⁇ heated in an atmosphere containing 95% N 2 - 5% H 2 at different temperatures from 750 to 800°C for times ranging from 1 to 10 minutes. After this heating stage the specimens were transferred from the hot zone of the furnace, cooled down to about 430°C and then introduced into a zinc alloy bath maintained at 430°C and protected by the 95% 2 - 5% H 2 atmosphere. They were maintained in the zinc bath for periods ranging from 5 to 60 seconds and then removed from the bath and cooled in a jet of 95% l ⁇ - - 5% H 2 gas.
  • This example relates to trials carried out with a pilot continuous annealing and galvanizing plant.
  • 800 kg coils of rimming steel sheet 150 mm wide and 0.25 mm thick were first treated in a Selas type furnace at temperatures ranging from 680 to 860°C.
  • the sheet was then cooled in a controlled atmosphere to about 430°C and then introduced into a seven-ton zinc bath.
  • the sheet was then nitrogen-gas wiped at the exit, jet cooled and finally coiled.
  • the speed of the sheet varied in the range 10 to 30 m/min.
  • the coating was uniform and free of bare spots, uncoated areas or other defects.
  • a Zn - 5% Al bath containing 0.13% Sn and as above 0.05% of cerium mischmetal was also used in the pilot galvanizing line.
  • the coatings obtained had characteristics similar to those described above with a coating somewhat less bright due to a different spangle behavior.
  • An additional bath containing Zn, 5% Al, 0.13% Sn, 0.05% Pb and about 0.05% Ce + La (added as Ce mischmetal or La mischmetal; or added as a master alloy containing about 20% Zn and 80% La and/or Ce mischmetals; or added as a master alloy containing about 90% Al and 10% La and/or Ce misch ⁇ metal) was also used in the pilot galvanizing line.
  • the coatings obtained showed a wide range of thickness, were uniform and again were free of bare spots and uncoated areas.
  • pilot plant conditions are mentioned as examples only and that other condi- tions prevailing in continuous annealing and galva ⁇ nizing lines as regards furnace type, composition of gas, speeds, wiping methods, etc., can be used with advantage with the zinc bath composition according to the invention.
  • bath and coating co posi- tions as described herein may be used in non- continuous (e.g. batch) galvanizing methods.
  • the formabili-fc'y and adherence was evaluated by means of bulge tests and Erichsen tests.
  • the coatings obtained with the isch- metal-containing bath exhibited an adherence and formability equivalent to that of standard galvanized coatings.
  • a 180° bending gave rise to no cracking and in the Erichsen test a depth of 9 mm was made on 0.25 mm thick sheets without peeling of the coating.
  • the corrosion resistance, in a salt spray test, of the Zn-Al coatings containing mischmetal was more than twice that of a standard galvanized coating of the same thickness.
  • the time to first rusting was about 900 hours instead of 350 hours with a conventional galvanized coating of the same thickness.
  • the corrosion resistance in an environment containing 10 ppm S0 2 was shown to be at least 50% greater than that of a conventional- galvanized coating.
  • the galvanic protection of the Zn-Al mischmetal coating was also determined by examining the progress of corrosion around scratches machined on specimens exposed to a S0 2 -containing environment.
  • the galvanic protection of the mischmetal-containing Zn - 5% Al coating was equal to that of a pure zinc coating and far superior to that of a coating containing Zn-55Al-1.5Si.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Coating With Molten Metal (AREA)

Abstract

An alloy for use in a zinc galvanizing bath comprising zinc, aluminum and a rare earth-containing alloy such as mischmetal. According to the preferred embodiments, the alloy contains from about 85% to about 97% zinc, from about 3% to about 15% aluminum and from about 5 ppm to about 1.0% mischmetal. The alloy may also contain one or more of the elements Fe, Pb, Sb, Mg, Sn, Cu and Si.

Description

Description
Zinc-Aluminum Alloys and Coatings
Technical Field
The present invention is directed to the appli- cation of zinc coatings to a substrate - commonly sheet steel.
The use of zinc as a protective coating has been known for many years. In this regard, hot dip galva¬ nizing, either continuous or batch type, has long been used for a variety of steel products to protect the products from corrosion.
Background Art
In order to obtain increased corrosion protec¬ tion as well as other advantages (e.g. better sacri- ficial protection of steel; improved for ability, weldability and paintability) efforts have been undertaken in the field of zinc coatings to develop improved zinc alloys for the continuous or batch application to substrates. Studies carried out in this direction have resulted in the development of new types of coatings such as the alloy Zn-55 Al- 1.5Si and other zinc alloys having low (i.e., less than 15%) Al-1.5Si content. The Zn-55 Al alloy coating developed by Bethlehem Steel (see for example U.S. Patent Nos. 3,343,930 and 3,393,089) reportedly exhibits a good corrosion resistance but, in view of its high aluminum content does not provide a satis¬ factory sacrificial protection of the steel substrate, Subsequent-s-fcudies have been aimed at modifying the composition of molten metal baths in order to form (by hot-dipping) a coating which improves corrosion resistance even in the most varied environ¬ ments. One of the aspects of these studies was the influence of the preparation of the surface to be coated on the quality of the product obtained. It thus appears that in order to ensure a quality coating, some of the alloy coatings previously developed required expensive preliminary surface treatments involving expensive equipment. For example, this was the case with respect to zinc coatings containing typically about 5% Al and addi¬ tions of other elements such as Sb, Pb + Mg, and Pb + Mg + Cu proposed by Inland Steel (see for example Inland U.S. Patent Nos. 4,029,478 and 4,056,366 as well as U.S. Patent No. 4,152,472 assigned to Nippon Steel) . There exists evidence showing that composi¬ tions of these types are characterized by a pro- nounced tendency to form bare-spots and similar defects even in the presence of careful surface preparation.
In view of the above considerations, there continues a need for a hot-dip metal bath of such composition that no special or expensive surface preparation of the substrate would be necessary and such that the protective coating obtained thereby is substantially free of bare spots or other defects.
Disclosure of the Invention Consistent with the above, there have been developed according to the present invention zinc- containing hot-dip metal baths which yield high quality protective coatings free of defects such as bare spots. Stated generally, the bath compositions and resultant coatings constitute improvements over known alloy" batha.-and coatings in that they contain additionally mixtures of rare earth elements. More particularly, the present invention is directed to zinc-aluminuπ compositions or alloys which have added thereto rare earths in the form of mischmetal. In this regard, it is preferred that the zinc-aluminum alloys be what are commonly referred to as low aluminum zinc alloys which are generally recognized to contain from about 3% to about 15% aluminum.
Detailed Description
The hot-dip metal baths according to the present invention, and hence the coatings obtained therefrom, may vary considerably just as known zinc-aluminum baths and coatings may vary. In each instance, however, it is essential that the bath have added thereto a mischmetal alloy in an amount sufficient to yield the improved results observed and described herein. A mischmetal addition to a zinc-aluminum bath in the range of from about 5 ppm to about 1.0%, and preferably about 0.01% to about 0.1% (by Weight), is generally contemplated as being sufficient in this regard.
As will be understood by one skilled in the art, the term mischmetal refers to a variety of knovm rare earth alloys. For example, two typical cerium mischmetals might have the following compositions (in weight %) :
(1) Ce 45-60; other rare earths 35-50, the balance comprising Fe, Mg, Al, Si and impurities.
(2) Ce 52.7, other rare earths 47.5, Fe 0.04, Mg 0.28, Al 0.08, Si 0.27 and the balance impurities.
Typical Lanthanum mischmetals can be defined by the following (in weight %) :
(1) a^ 60-90; Ce 8.5; Nd 6.5; Pr 2 the balance comprising Fe, Mg, Al and Si as well as possible impurities.
(2) La 83, Ce 8.5, Nd 6.5, Pr 2, Fe 0.2, Mg 0.03, Al 0.18, Si 0.43 and the balance impurities. Thus the term mischmetal, as used herein, refers to the above compositions as well as other mischmetal compositions readily apparent to those skilled in the art. As stated above, the preferred alloy to which mischmetal is to be added is a zinc-aluminum alloy containing from about 3% to about 15% aluminum. Such alloys typically contain about 5% aluminum. These alloys may contain constituents in addition to mischmetal such as Fe, Pb, Sb, Mg, Sn, Cu and Si.
Thus one embodiment of the invention comprises a low aluminum (i.e., 3-15%) zinc bath containing Pb or Sn as well as mischmetal. Pb and Sn are known additives to galvanizing baths for modifying the fluidity of the liquid metal or the spangle of the solidified coating.
The addition of Sb to a galvanizing bath is dis¬ closed in U.S. Patent No. 4,056,366 to improve the coatability of Zn-Al coatings in a manner similar to lead but without the deleterious effect that lead has upon the intergranular corrosion of the coatings. The addition of Sb to the mischmetal-containing compositions according to the present invention is therefore contemplated. Moreover, a Zn-Al composition containing Pb together with Sb is within the scope of the invention. A typical composition might contain 3-15% Al, 0.03-0.15% Sb, less than 0.02% Pb, and the balance Zn to which mischmetal has been added.
Zinc-aluminum alloys containing lead and also Mg and Cu are reported to be immune to grain boundary corrosion. In this type of coating alloys, mischmetal additions have been shown to exhibit a pronounced beneficial effect as regards soundness and uniformity.' Thus a Zn-Al alloy containing Mg, Pb, Cu and misch- metal is encompassed by the present invention. Here a typical composition might contain 3-15% Al, 0.02- 0.15% Mg, 0.02-0.15% Pb and possibly 0.1-0.3% Cu, the balance being Zn with mischmetal additions.
Various mischmetals may be advantageously used according to the invention, including mixtures of mischmetals in a single zinc bath or coating. For example, a La-mischmetal and a Ce-mischπietal may be added simultaneously, preferably in an amount such that the total mischmetal concentration is within the ranges described above, i.e. from about 5 ppm to about 1.0% and preferably from about 0.01 to 0.1% by weight. In order to facilitate the addition of the mischmetal to the galvanizing bath, a master alloy may be first prepared and then added to the zinc bath so as to yield the desired mischmetal concentration. Such master alloys might be comprised of 20% Zn and 80% mischmetal or 85-95% Al and 15-5% mischmetal.
EXAMPLES 1. Specimens of rimming steel sheet measuring 68 x 120 x 0.7 mm were galvanized in a device simulating a continuous galvanizing bath. They were first pre¬ heated in an atmosphere containing 95% N2 - 5% H2 at different temperatures from 750 to 800°C for times ranging from 1 to 10 minutes. After this heating stage the specimens were transferred from the hot zone of the furnace, cooled down to about 430°C and then introduced into a zinc alloy bath maintained at 430°C and protected by the 95% 2 - 5% H2 atmosphere. They were maintained in the zinc bath for periods ranging from 5 to 60 seconds and then removed from the bath and cooled in a jet of 95% l~- - 5% H2 gas.
Such tests were carried out with different types of bath compositions. The galvanized samples were examined to determine the soundness of the coating, particularly as regards the occurrence of bare spots and uncoated areas. In a bath containing 5 to 8% Al without any other additions, the specimens contained a high pro¬ portion of uncoated areas and bare spots. This was the case even as to the specimens pretreated at the highest temperature and longest annealing time in the reducing atmosphere. The addition of 0.15% Sb in a Zn-5% Al bath resulted in a decrease in the amount of bare spots but still up to 33% of the galvanized faces presented bare spots. A third bath containing 5% Al and 0.02% Ce added as Ce-mischmetal resulted in 100% good coatings for a range of heat treating conditions.
A bath containing Zn - 5% Al, 0.03 La and 0.025 Ce added as La and Ce mischmetal gave rise to 100% good coatings even for preheating temperatures as low as 750°C.
2. This example relates to trials carried out with a pilot continuous annealing and galvanizing plant. In these trials 800 kg coils of rimming steel sheet 150 mm wide and 0.25 mm thick were first treated in a Selas type furnace at temperatures ranging from 680 to 860°C. The sheet was then cooled in a controlled atmosphere to about 430°C and then introduced into a seven-ton zinc bath. The sheet was then nitrogen-gas wiped at the exit, jet cooled and finally coiled.
Depending on test conditions the speed of the sheet varied in the range 10 to 30 m/min.
Several coils were galvanized with a bath con¬ taining Zn - 5% Al and a cerium mischmetal content from 0.05% - 0.001%. The cerium content varied from 0.04% to 0.0008% and the La content was 0.02% to 0.0002%. The resulting coating was bright with a grain size varying from 1 to 5 mm, depending on the cooling conditions, and with thicknesses varying from 5 to 35 m depending on the gas wiping conditions. -7-
The coating was uniform and free of bare spots, uncoated areas or other defects.
A Zn - 5% Al bath containing 0.13% Sn and as above 0.05% of cerium mischmetal was also used in the pilot galvanizing line. The coatings obtained had characteristics similar to those described above with a coating somewhat less bright due to a different spangle behavior. An additional bath containing Zn, 5% Al, 0.13% Sn, 0.05% Pb and about 0.05% Ce + La (added as Ce mischmetal or La mischmetal; or added as a master alloy containing about 20% Zn and 80% La and/or Ce mischmetals; or added as a master alloy containing about 90% Al and 10% La and/or Ce misch¬ metal) was also used in the pilot galvanizing line. The coatings obtained showed a wide range of thickness, were uniform and again were free of bare spots and uncoated areas.
It is evident that the pilot plant conditions are mentioned as examples only and that other condi- tions prevailing in continuous annealing and galva¬ nizing lines as regards furnace type, composition of gas, speeds, wiping methods, etc., can be used with advantage with the zinc bath composition according to the invention. Moreover, bath and coating co posi- tions as described herein may be used in non- continuous (e.g. batch) galvanizing methods.
3. Specimens from the above pilot plant trials were subjected to various trials for the evaluation of formability and adherence, the corrosion resistance in various environments, the galvanic protection, and the microstructure.
The formabili-fc'y and adherence was evaluated by means of bulge tests and Erichsen tests. In both types of tests the coatings obtained with the isch- metal-containing bath exhibited an adherence and formability equivalent to that of standard galvanized coatings. For example a 180° bending gave rise to no cracking and in the Erichsen test a depth of 9 mm was made on 0.25 mm thick sheets without peeling of the coating.
The corrosion resistance, in a salt spray test, of the Zn-Al coatings containing mischmetal was more than twice that of a standard galvanized coating of the same thickness. For example, with the coatings of the present invention the time to first rusting was about 900 hours instead of 350 hours with a conventional galvanized coating of the same thickness.
Similarly the corrosion resistance in an environment containing 10 ppm S02 was shown to be at least 50% greater than that of a conventional- galvanized coating. The galvanic protection of the Zn-Al mischmetal coating was also determined by examining the progress of corrosion around scratches machined on specimens exposed to a S02-containing environment. The galvanic protection of the mischmetal-containing Zn - 5% Al coating was equal to that of a pure zinc coating and far superior to that of a coating containing Zn-55Al-1.5Si.

Claims

1. An alloy for use in a galvanizing bath for pro¬ viding a protective coating on a substrate, said alloy comprising zinc, aluminum and a rare earth- containing alloy.
2. An alloy according to claim 1 wherein the rare earth-containing alloy is mischmetal.
3. An alloy according to claim 2 comprising from about 85% to about 97% zinc, from about 3% to about 15% Al and mischmetal.
4. An alloy according to claim 3 containing from about 5 ppm to about 1.0% mischmetal.
5. An alloy according to claim 4 containing from about 0.01 to about 0.1% mischmetal.
6. An alloy according to claim 4 wherein the misch¬ metal is Ce-mischmetal or La-mischmetal.
7. An alloy according to claim 5 wherein the misch¬ metal is Ce-mischmetal or La-mischmetal.
8. An alloy according to claim 4, said alloy con- taining additionally at least one of the elements selected from the group consisting of Fe, Pb, Sb, Mg, Sn, Cu, and Si.
9. An alloy aeαprding to claim 4, said alloy con¬ taining additionally antimony. ■
10. An alloy according to claim 9, said alloy con¬ taining additionally lead. -lO-
11. An alloy according to claim 10 containing from about 0.03-0.15% Sb and less than 0.02% Pb.
12. An alloy according to claim 4, said alloy con¬ taining additionally Mg and Pb.
13. An alloy according to claim 12 containing from about 0.02-0.15% Mg and from about 0.02-0.15% Pb.
14. An alloy according to claim 13, said alloy con¬ taining additionally Cu.
15. An alloy according to claim 14, containing from about 0.1-0.3% Cu.
16. An alloy according to claim 6 wherein said misch¬ metal is a Ce-mischmetal comprising from about 45-60% Ce, from about 35 to 50% other rare earths, and the balance comprising Fe, Mg, Al, Si and impurities.
17. An alloy according to claim 6 wherein said misch¬ metal is a Ce-mischmetal comprising 52.7% Ce, other rare earths 47.5%, Fe 0.04%, Mg 0.28%, Al 0.08%, Si 0.27% and the balance impurities.
18. An alloy according to claim 6 wherein said misch¬ metal is a La-mischmetal comprising 60-90% La, 8.5% Ce, 6.5% Nd, 2% Pr, and the balance com¬ prising Fe, Mg, Al and Si and impurities.
19. An alloy according to claim 18 wherein said misch- metal comprises 83% La, 8.5% Ce, 6.5% Nd, 2% Pr, ■ 0.2% Fe, 0.03% Mg, 0.18% Al, 0.43% Si and the balance impurities. 20. An alloy according to claim 4 wherein said misch¬ metal is added to the alloy in the form of a master alloy.
21. An alloy according to claim 20 wherein said master alloy comprises 20% Zn and 80% mischmetal.
22. An alloy according to claim 20 wherein said master alloy comprises about 85-95% Al and about 5-15% mischmetal.
EP19810901054 1980-03-25 1981-03-18 Zinc-aluminum coatings Expired EP0048270B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT81901054T ATE14900T1 (en) 1980-03-25 1981-03-18 ZINC-ALUMINUM COATINGS.

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
BE47115 1980-03-25
BE6/471152A BE882431A (en) 1980-03-25 1980-03-25 ZINC-ALUMINUM COATING FORMATION PROCESS
BE47373 1981-01-16
BE6047373 1981-01-16

Publications (3)

Publication Number Publication Date
EP0048270A1 EP0048270A1 (en) 1982-03-31
EP0048270A4 true EP0048270A4 (en) 1982-07-12
EP0048270B1 EP0048270B1 (en) 1985-08-14

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Family Applications (1)

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Country Status (6)

Country Link
EP (1) EP0048270B1 (en)
JP (1) JPH0124221B2 (en)
BR (1) BR8107944A (en)
CA (1) CA1175686A (en)
IN (1) IN156009B (en)
WO (1) WO1981002748A1 (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE890256A (en) * 1981-09-07 1982-03-08 Centre Rech Metallurgique IMPROVEMENTS IN GALVANIZING PROCESSES FOR STEEL SHEETS OR STRIPS
EP0148740A1 (en) * 1983-12-22 1985-07-17 CENTRE DE RECHERCHES METALLURGIQUES CENTRUM VOOR RESEARCH IN DE METALLURGIE Association sans but lucratif Method for hot coating and bath composition therefor
EP0958395A1 (en) * 1996-05-02 1999-11-24 N.V. Bekaert S.A. Chromium-silicon spring wire
JP3343498B2 (en) * 1997-06-13 2002-11-11 昭和電工株式会社 Low temperature brazing filler metal
JP4136286B2 (en) * 1999-08-09 2008-08-20 新日本製鐵株式会社 Zn-Al-Mg-Si alloy plated steel with excellent corrosion resistance and method for producing the same
WO2001064971A1 (en) * 2000-02-29 2001-09-07 Nippon Steel Corporation Plated steel product having high corrosion resistance and excellent formability and method for production thereof
CN115874075B (en) * 2022-12-16 2023-10-13 佛山市桂源锌合金材料有限公司 Low-impurity and easy-to-polish zinc alloy and preparation process thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1095832A (en) * 1964-03-06 1967-12-20 Fur Zinkindustrie Ag Improvements in the protection of ferrous constructions against corrosion
FR1570613A (en) * 1967-04-18 1969-06-13
GB1195904A (en) * 1966-07-11 1970-06-24 Cominco Ltd Process for the production of Coloured Coatings
FR2078812A5 (en) * 1970-02-26 1971-11-05 Centre Nat Rech Metall Malleable binary alloys of zinc and rare - earths

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE926654C (en) * 1951-10-31 1955-04-21 Goldschmidt Ag Th Safety flintstones for mine lamps in fire-weather endangered mining operations
US2829973A (en) * 1953-04-09 1958-04-08 Magnesium Elektron Ltd Magnesium base alloys
FR1155357A (en) * 1956-08-02 1958-04-25 Treibacher Chemische Werke Ag Process for spinning pyrophoric ferrocerium alloys
US3343930A (en) * 1964-07-14 1967-09-26 Bethlehem Steel Corp Ferrous metal article coated with an aluminum zinc alloy
GB1115673A (en) * 1964-07-14 1968-05-29 Bethlehem Steel Corp Zinc-aluminum coated products and methods therefor
US3527601A (en) * 1967-06-14 1970-09-08 Dow Chemical Co Process of making creep-resistant zinc-base alloys
LU55104A1 (en) * 1967-12-15 1969-07-17
US4152472A (en) * 1973-03-19 1979-05-01 Nippon Steel Corporation Galvanized ferrous article for later application of paint coating
US4056366A (en) * 1975-12-24 1977-11-01 Inland Steel Company Zinc-aluminum alloy coating and method of hot-dip coating
US4029478A (en) * 1976-01-05 1977-06-14 Inland Steel Company Zn-Al hot-dip coated ferrous sheet
US4213799A (en) * 1978-06-05 1980-07-22 Swiss Aluminium Ltd. Improving the electrical conductivity of aluminum alloys through the addition of mischmetal

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1095832A (en) * 1964-03-06 1967-12-20 Fur Zinkindustrie Ag Improvements in the protection of ferrous constructions against corrosion
US3383297A (en) * 1964-03-06 1968-05-14 Eberius Ernst Zinc-rare earth alloy anode for cathodic protection
GB1195904A (en) * 1966-07-11 1970-06-24 Cominco Ltd Process for the production of Coloured Coatings
FR1570613A (en) * 1967-04-18 1969-06-13
FR2078812A5 (en) * 1970-02-26 1971-11-05 Centre Nat Rech Metall Malleable binary alloys of zinc and rare - earths

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO8102748A1 *

Also Published As

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JPS57500475A (en) 1982-03-18
EP0048270A1 (en) 1982-03-31
CA1175686A (en) 1984-10-09
IN156009B (en) 1985-04-27
BR8107944A (en) 1982-03-09
EP0048270B1 (en) 1985-08-14
WO1981002748A1 (en) 1981-10-01
JPH0124221B2 (en) 1989-05-10

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