AU628042B2 - Hot-dip zinc-aluminum alloy coated steel sheet for prepainted steel sheet, process for producing the same and prepainted steel sheet - Google Patents

Hot-dip zinc-aluminum alloy coated steel sheet for prepainted steel sheet, process for producing the same and prepainted steel sheet Download PDF

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AU628042B2
AU628042B2 AU32886/89A AU3288689A AU628042B2 AU 628042 B2 AU628042 B2 AU 628042B2 AU 32886/89 A AU32886/89 A AU 32886/89A AU 3288689 A AU3288689 A AU 3288689A AU 628042 B2 AU628042 B2 AU 628042B2
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steel sheet
hot
aluminum alloy
bath
prepainted
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Toru Kameya
Koji Ohta
Yuuji Okuzaki
Hisanori Shimizu
Masaaki Takagi
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Taiyo Steel Co Ltd
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    • 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
    • C23C2/26After-treatment
    • C23C2/28Thermal after-treatment, e.g. treatment in oil bath
    • C23C2/285Thermal after-treatment, e.g. treatment in oil bath for remelting the coating
    • 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
    • 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
    • C23C2/14Removing excess of molten coatings; Controlling or regulating the coating thickness
    • C23C2/16Removing excess of molten coatings; Controlling or regulating the coating thickness using fluids under pressure, e.g. air knives
    • C23C2/18Removing excess of molten coatings from elongated material
    • C23C2/20Strips; Plates
    • 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
    • C23C2/26After-treatment
    • C23C2/28Thermal after-treatment, e.g. treatment in oil bath
    • C23C2/29Cooling or quenching
    • 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
    • C23C2/34Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the shape of the material to be treated
    • C23C2/36Elongated material
    • C23C2/40Plates; Strips
    • 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
    • C23C22/00Chemical 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
    • C23C22/05Chemical 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 using aqueous solutions
    • C23C22/06Chemical 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 using aqueous solutions using aqueous acidic solutions with pH less than 6
    • C23C22/24Chemical 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 using aqueous solutions using aqueous acidic solutions with pH less than 6 containing hexavalent chromium compounds
    • 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
    • C23C22/00Chemical 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
    • C23C22/78Pretreatment of the material to be coated

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  • Chemical & Material Sciences (AREA)
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  • Engineering & Computer Science (AREA)
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Description

-1 9K 4 7 P4 OPI DATE 03/11/89 32886 89 APPLN. ID AOJP DATE 30/11/89
INTERNATIC
PCT NUMBER PCT/JP89/00291
EATY(PCT)
(51) Inernational Patent Classification 4 (11) International Publication Number: WO 89/09844 C23C 2/06, 2/20, 2/28 Al C23C 22/78 (43) International Publication Date: 19 October 1989 (19.10.89) (21) International Application Number: PCT/JP89/00291 (74) Agents: NIIBE, Koji et al.; Room 330, Marunouchi-Yaesu Bldg., 6-2, Marunouchi 2-chome, Chiyoda-ku, Tokyo (22) International Filing Date: 17 March 1989 (17.03.89) 100 (JP).
Priority data: (81) Designated States: AU, BE (European patent), DE (Euro- 63/89998 12 April 1988 (12.04.88) JP pean patent), FI, FR (European patent), GB (European patent), IT (European paten'), KR, NL (European patent), SE (European patent), US.
(71)Applicant (for all designated States except US): TAIYO STEEL CO., LTD. [JP/JP]; 7-2, Nihonbashi-Honmachi 1-chome, Chuo-ku, Tokyo 103 Published With international search report.
(72) Inventors; and Inventors/Applicants (for US only) KAMEYA, Toru [JP/ JP]; 19-18, Makuhari-Hongo 2-chome, Chiba-shi, Chiba 281 SHIMIZU, Hisanori [JP/JP]; 21-17, Makuhari- Hongo 2-chome, Chiba-shi, Chiba 281 TAKAGI, Masaaki [JP/JP]; 7-6, Tamanoi-cho, Atsuta-ku, Nagoyashi, Aichi 456 OKUZAKI, Yuuji [JP/JP]; 1571-13, Usui, Sakura-shi, Chiba 285 OHTA, Koji [JP/JP]; 883-2-232, Kanasugi-cho, Funabashi-shi, Chiba 273 (JP).
(54)Title: HOT-DIP ZINC-ALUMINUM ALLOY COATED STEEL SHEET FOR PREPAINTED STEEL SHEET, PRO- CESS FOR PRODUCING THE SAME AND PREPAINTED STEEL SHEET (57) Abstract A hot-dip zinc-aluminum alloy coated steel sheet produced by coating in a hot dipping bath comprising 0.3 to 3.5 wt.% of Al, 100 ppm or less of Pb and the balance of Zn and unavoidable impurities is provided. The bath may further contain specified amounts of Si as well as Mg, Mn and/or Cu. A process for producing said coated steel sheet is also provided, wherein the temperature of the steel sheet to be dipped into the hot dipping bath is adjusted to be lower than the bath temperature and, if necessary, the amount of the molten zinc-aluminum alloy deposited on the steel sheet is controlled with a special gas wiping type of equipment and, if necessary, the coated steel sheet is reheated at a temperature higher than the melting temperature of the coating layer. A prepainted steel sheet prepared from this steel sheet is also provided.
w I WO89/09844 PCT/JP89/00291
DESCRIPTION
HOT-DIP ZINC-ALUMINUM ALLOY COATED STEEL SHEET FOR PREPAINTED STEEL SHEET, PROCESS FOR PRODUCING THE SAME AND PREPAINTED STEEL SHEET Technical Field: The present invention relates to prepainted steel sheets having excellent properties suitable for use as construction materials such as roof materials and wall materials as well as household electric appliances, hot-dip zinc-aluminum alloy coated steel sheets having properties superior to those of conventional ones and suitable for use as the sheets of the prepainted sheets and a process for producing them.
Background Art: Steel sheets coated with zinc (Zn) or prepainted steel sheets produced therefrom have been used in construction materials or household electric appliances.
Further steel sheets coated with zinc-aluminum (Zn-Al) alloy attract attention as materials taking the place of Zn coated steel sheets, since they have corrosion resistance, etc. superior to those of the Zn coated ones.
Various processes have been proposed heretofore for producing the Zn-Al alloy coated steel sheets. These processes include one comprising the use of a coating bath comprising 5 to 25 wt.% of Al, 0.1 wt.% or less 1 1 WO 89/09844 PCT/JP89/00291 2 of Pb and the balance of Zn (see Japanese Patent Publication No. 25220/1976); one comprising the use of a coating bath comprising more than 3.5 wt.% but not more than 10 wt.% of Al, and Mg, Be, Ti and Cu each in a specified range of a small amount relative to the concentration of Pb, Sn or both of them in the coating bath (see Japanese Patent Publication No. 47055/1978); one comprising the use of a coating bath comprising 3 to 15 wt.% of Al, about 85 to 97 wt.% of Zn and small amounts of rare earth elements (see Japanese Patent Publication No. 500475/1982); and one comprising the use of a coating bath comprising 0.05 to 2.0 wt.% of Al, 0.01 to 0.1 wt.% of Mn and the balance of Zn and unavoidable impurities (see Japanese Patent Publication No. 32700/1985).
A principal object of these processes is to reduce the weight loss of the coated steel sheets due to corrosion by the addition of Al.
The loss due to corrosion of the coated steel sheets in exposure tests in outdoor is usually reduced as the Al concentration in the coating bath is increased and, therefore, the corrosion resistance of the sheets is improved. However, an alloy layer formed on the interface with iron becomes thicker and the adhesion and the workability of the coating layer are seriously reduced as the Al concentration is increased.
Methods have been proposed to solve these problems by adding small amounts of various elements.
WO 89/09844 PCT/JP89/00291 3 However, they have problems that the use of the limited kinds of elements in limited amounts is troublesome, that the coating pot must be exchanged in order to switch over the coating bath and that the appearance of the coated steel sheet surface is impaired. Under these circumstances, the development of a process for producing coated steel sheets which can satisfy the required qualities with as little as possible elements added is demanded.
The following properties are required of Zn-Al alloy coated steel sheets, particularly those to be used as sheets for prepainted steel sheets from the viewpoint of the use of them: the corrosion resistance of the steel sheet surface is improved, a self-sacrificing rust-preventive power of Zn for that part of iron which is exposed when the steel sheet is cut is retained, no crack is formed in a bent part of the steel sheet in the working step, the coating layer has an excellent adhesion which is not reduced with time, and the surface smoothness is excellent.
The present applicant proposed a coated steel sheet for prepainted galvanized steel sheets which is produced by coating a steel sheet with hot dipping bath comprising 0.3 to 3.5 wt.% of Al and the balance of Zn and unavoidable impurities (see Japanese Patent 4 Application No. 159469/1983).
It is apparent from the phase diagram of Zn-Al alloy that the eutectic point is realized when the alloy comprises 5 wt.% of Al (95 wt.% of Zn). When the Al content is deviated to some extent from 5 the texture of the solidified alloy is quite different from that of the wt.% Al ally unless it is quenched at a very high speed.
The Al-Zn alloy having 5 wt.% Al content is eutectic and, therefore, its melting point is low and Al and Zn are dispersed homogeneously irrespective of the cooling rate.
However, when the Al content is less than 5 for example, 1 a primary crystal of Zn containing only very small amount of the Al component is formed in the coating layer and the majority of the Al component remains in the finally solidified grain boundary. Thus no coating layer having homogenous composition is formed. It has been believed that an Al-Zn alloy having an Al content of 5 wt.% is advantageous for homogenously dispersing Al and Zn and for giving a stable texture.
Prepainted steel sheets are those previously painted with a paint. They are produced continuously on a large scale by painting galvanised steel sheets or zinc alloy coated steel sheets with a roll coater usually after chemical conversion treatment. The demand for prepainted steel sheets as starting materials for construction materials, household electric appliances, business *6A machines, etc. is now increasing, since they have excellent, uniform qualities, they can be supplied in large amounts and no painting is necessary after application.
The properties required of the prepainted steel sheets are mainly adhesion, corrosion resistance, workability, weather resistance and scratch resistance.
However, it is quite difficult to satisfy all of the required properties with only one paint.
Thus, it was a usual practice to classify paints into two groups in the prior art, i.e. those for under-painting which could impart adhesion and corrosion resistance and paints for toppainting which could impart workability, weather resistance and scratch resistance to further improve the qualities and properties of the :prepainted steel sheets. These paints are applied by the so-called two-coat two-bake process wherein the sheets were baked after application of the under-painting paint and *baked again after application of the toppainting paint in e00V order to improve the qualities of the prepainted steel "sheets.
However, recently, durability over a period of as long as, for example, 10 or 20 years is demanded of the construction materials such as roof and wall materials in various cases.
The term "durability" as used herein means weather resistance and corrosion resistance. Namely, an excellent durability means that the color tone and gloss are /q pre.
"lr 6 substantially unchanged and no rust is formed in 10 or years.
The excellent weather resistance can be given by using a paint having excellent properties against chalking and fading.
However, it is difficult to inhibit the rust formation over a long period of time.
The formation of red rust is often observed in a portion of roof or wall material worked by roll forming machine only several years after the construction, though the timing of the rust formation varies depending on the environmental conditions.
Such rust formation occurs even when the material is exposed to the outdoor for only a short period of timne, since cracks are formed in the worked part already prior to the use and in an extreme case, the steel texture is exposed through the cracks formed in the coating layer.
To solve this problem, it is necessary to cover the coating layer with a painting film having such an excellent elongation that it can withstand the deformation in the i course of working and to use a steel sheet having a coating layer having such an excellent workability that it is not cracked in the course of working.
DISCLOSURE OF THE INVENTION After intensive investigations, the inventors have succeeded in the production of Zn-Al alloy coated steel sheets having excellent properties. After further investigations of prepainted steel sheets, the inventors have found that two-coat steel sheets having a performance equivalent to that of three-coat steel sheets can be produced when the Zn-Al alloy coated steel sheets prepared by the present invention are used.
Thus the invention relates to a process for the preparation of a hot-dip zinc-aluminum alloy coated steel sheet suitable for a prepainted steel sheet, comprising coating a steel sheet in a hot dipping bath comprising 0.3 to 3.5 wt.% of Al, 100ppm or less of Pb and the balance of Zn and incidental impurities, wherein the temperature of *the steel sheet dipped in the hot dipping bath is lower than that of the hot dipping bath, and taking the steel sheet out of the hot dipping bath, wherein the amount of the molten zinc-aluminum alloy deposited on the steel sheet is controlled with a gas wiping type of equipment for controlling the amount of molten zinc-aluminum alloy deposit under conditions comprising a slit clearance of 0.6 to 2.4 mm, a distance between front and back nozzles of g.i to 40 mm and an ejecting pressure of gas of 0.1 to kg/cm 2 The invention also relates to a process for the preparation of a hot-dip zinc-aluminum alloy coated steel sheet suitable for a prepainted steel sheet, comprising coating a steel sheet in a hot dipping bath comprising 0.3 to 3.5 wt.% of Al, i00ppm or less of Pb and the balance of 8 Zn and incidental impurities, wherein the temperature of the steel sheet dipped in the hot dipping bath is lower than that of the hot dipping bath, reheating the hot-dip zinc-aluminum alloy coated steel sheet to a temperature above the melting temperature of the coating layer and cooling the hot-dip zinc-aluminum alloy coated steel sheet to the solidifying point thereof at a rate of at least 100C/sec.
BRIEF DESCRIPTION OF THE DRAWINGS .Figs. l(a) to are microphotographs of the metal textures on the surfaces of the coating layers formed in Example 5. They are X-ray images of Al on the surface obtained with EPMA. Figs. 1(b) and 1(c) are microphotographs of the metal textures of the coating layer surfaces obtained when (steel sheet temperature at dipping time) (bath temperature) was 20°C, -20 0 °C and -80 0
C,
respectively.
Figs. 2(a) and show the concentration distribution of Fe, Zn and Al in the thickness direction of the hot-dip zinc-aluminum alloy coated steel sheets produced in Example 5. They show the concentration distributions obtained when (steel sheet temperature at dipping time) (bath temperature) was 20 0 C and -80 0
C,
respectively.
Fig. 3 is a schematic drawing of the hot dipping S equipment used in Example 6.
.4 9 Figs. 4(a) to are microphotographs of the appearances of the metal textures of the coating layer surfaced formed in Example 7. Fig. 4(a) is a microphotograph of the metal texture of the coating layer surface formed under conditions comprising (steel sheet temperature at dipping time) (bath temperature) of -60 0
C,
a nozzle slit clearance of 0.8mm, an ejecting pressure of gas of 1.0 kg/cm 2 and a distance between front and back nozzles of 50 mm. Fig. 4(b) is one formed under conditions comprising (steel sheet temperature at dipping time) (bath temperature) of -20°C, a nozzle slit clearance of 0.6 mm, an ejecting pressure of gas of 1.5 kg/cm 2 and a distance between front and back nozzles of 20 mm. Fig.
4(c) is one formed under conditions comprising (temperature i" of steel sheet at dipping time) (bath temperature) of -80 0 C, a nozzle slit clearance of 1.2 mm, an ejecting pressure of gas of 0.1 kg/cm 2 and a distance between front and back nozzles of 20 mm.
Figs. 5(a) and show the thickness distributions *of the coating layers, wherein Fig. 5(a) shows that of the Example) and Fig. 5(b) shows that of the deposit coating layer having a surface reheated at 460 0 C (Example 8).
Figs. 6(a) to are microphotographs of the metal textures of the coating layer surfaces obtained in Example 9. They are X-ray images of Al on the surface obtained with EPMA. Figs. 6(b) and 6(c) are microphotographs i of the metal textures of the coating layer surfaces obtained when the cooling speed was 2 0 C/sec, 170C/sec and 47 0 C/sec, respectively.
BEST MODE FOR CARRYING OUT THE INVENTION The invention relates to a hot-dip zinc-aluminum alloy coated steel sheet for a prepainted steel sheet, which is produced by coating in a hot dipping bath comprising 0.3 to 3.5 wt.% of Al, 100ppm or less of Pb and the balance of Zn and incidental impurities.
The Al concentration is thus limited because when it exceeds 3.5 the self-sacrifying anticorrosive effect of Zn on iron is reduced while when it is t e insufficient, the effect of improving the corrosion resistance at the surface of the coating layer is unsatisfactory. With at least 0.3 wt.% Al concentration, b WO 89/09844 PCT/JP89/00291
I
the workability is also improved and this effect is remarkable when the Al concentration is 0.5 wt.% or higher.
The Pb concentration is limited because when it exceeds 100 ppm, the adhesion is reduced with time due to intercrystalline corrosion and consequently the corrosion resistance which is particularly important for the prepainted steel sheet is damaged. With 100 ppm or less of Pb, stable adhesion which is not reduced with time can be obtained. With an Al concentration of 0.3 to 3.5 wt.% and a Pb concentration of 100 ppm or less, a zinc-aluminum alloy coated steel sheet which does not cause reduction in adhesion with time, has an excellent workability and is quite suitable for use as the sheet for a prepainted steel sheet can be obtained.
The temperature of the hot dipping bath may be one at which Zn and Al are molten to form a homogeneous melt, such as about 430 to 480 0
C.
e n co po S -s The invention ac sot forth in Claim 2 rlatc a hot-dip zinc-aluminum alloy coated steel sheet for a prepainted steel sheet, which is produced by coating in a hot dipping bath comprising 0.3 to 3.5 wt.% of Al, 1/100 to 1 part, per part of Al, of Si, 100 ppm or less in e no\ of Pb and the balance of Zn and unaveidablieimpurities.
Although a hot-dip zinc-aluminum alloy coated steel sheet having excellent workability and adhesion after aging can be obtained when the Al concentration S is in the range of 0.3 to 3.5 wt.% and the Pb r WO 89/09844 PCT/JP89/00291 concentration is 100 ppm or less as stated in C-laim 1, it is further preferred to add 1/100 to 1 part, per part of Al, of Si. The addition of Si serves to inhibit the formation of the alloy layer at the interface between the steel sheet and the coating layer to thereby make the formation of a thin alloy layer possible. Thus, a zinc-aluminum alloy coated steel sheet having further improved workability and adhesion after aging can be obtained.
The Si concentration is limited because when it is as low as about 1/200 of the Al concentration, no improvement in the workability or adhesion can be obtained. Another reason is that the control of the addition of Si in an amount of as small as 1/200 of Al is difficult, since the Al concentration is as low as 0.3 wt.% or less. The lower limit of the Si concentration is thus 1/100 of the Al concentration.
The Al concentration is limited for the same reasons a: those of Claim 1.
C0Aso encompc.SSeS The inventionj iCatda inClaim r 3 elates- to a hot-dip zinc-aluminum alloy coated steel sheet for a prepainted steel sheet, which is produced by coating cescried- cbovein the same hot dipping bath as that of Claim 1 or 2, which further contains 0.01 to 1.5 wt.% of one or more metals selected from the group consisting of Mg, Mn and Cu.
When metallic elements effective in improving the corrosion resistance of the galvanized steel sheet, YWO 89/09844 PCT/JP89/00291 123 such as Mg, Mn or Cu, are added to the bath, the effects of the present invention, i.e. satisfactory workability, corrosion resistance and adhesion after aging are further improved. With 0.01 wt.% or more of the metallic elements, the effects can be obtained. The addition of the metallic elements in an amount larger than 1.5 wt.% is not preferred from the viewpoint of the cost or efficiency of working. Mg, Mn and Cu may be used alone or in combination of them. By adjusting the amount of Pb to 100 ppm or less, a stable adhesion after aging can be attained.
c*Xso e.nc-omQpcsses The invention stated in Claim 4 relatoe to a process for producing a hot-dip zinc-aluminum alloy coated steel sheet for a prepainted steel sheet, wherein the temperature of the starting steel sheet dipped in the hot dipping bath is lower than that of the bath in the step of coating in the hot dipping bath ie G One, 1\ to claim 1, 2 3. Th'-feature of the invention -ta-tedin Claim 4 resides in that the temperature of the steel sheet dipped in the hot dipping bath at the dipping time is adjusted to a temperature lower than that of the bath.
Preferably, the temperature of the steel sheet to be dipped in the hot-dip Zn-Al alloy coating bath is adjusted to a temperature lower than the bath temperature by at most 80 0 C, particularly by 10 to 60*C. By this process, a hot-dip zinc-aluminum alloy coated steel sheet having an excellent surface corrosion resistance and a high power of protecting the edge of the steel from rust is
L-
i WO 89/09844 PCT/JP89/0291 obtained. Also the corrosion resistance in a bent part is improved.
Usually in the production of a hot-dip coated steel sheet in hot dipping equipment provided with a continuous annealing furnace, the temperature of the steel sheet to be dipped in a hot dipping bath is kept higher than a temperature of the bath from the viewpoints of the adhesion and the heating effect of the bath.
Since the steel sheet is thicker than the coating layer and the temperature of the steel sheet is high, the cooling of the coating layer starts with its surface and the interface of the coating layer with the steel sheet is solidified layer. Consequently, the Al concentration is high in the interface and the thickness of the alloy layer is increased to thereby reduce the workability and the self-sacrificing anticorrosive effect on the steel, while the Al concentration on the coating layer surface is low to reduce the corrosion resistance.
In the invention stated in Claim, 4, the temperature of the steel sheet dipped in the hot dipping bath is kept below the bath temperature contrary to the conventional processes in order to initiate the cooling of the coating metal on the side facing to the steel sheet. By this process, the inventors have succeeded in reducing the Al concentration on the interface side and reducing the amount of the alloy layer formed. In 4 this process, the self-sacrificing anticorrosive power S(resistance to the initial red rust formation) of Zn WO 89/09844 PCT/JP89/00291 is retained. Further, since the alloy layer formed is thin, no crack is formed in the bent part.
On the other hand, the Al concentration in the surface region of the coating layer is increased and, therefore, the corrosion resistance of the surface is improved (namely, the weight loss due to corrosion is reduced).
The feature of the present invention thus resides in that the temperature of the steel sheet to be dipped in the hot-dip Zn-Al alloy coating bath is kept below the temperature of the bath and the temperature of the steel sheet to be pulled out of the bath is kept below the bath temperature as far as possible in order that the solidification of the coating layer be started with the part in contact with the steel sheet and is completed as soon as possible. Such a process has never been known as yet.
The hot dipping bath temperature is such that Zn and Al are molten to form a homogeneous melt, for example, about 430 to 480°C.
The temperature of the steel sheet to be dipped in the hot dipping bath is preferably kept below the bath temperature by 10 to 80'C. For example, when the bath temperature is 480 0 C, the temperature of the steel sheet to be dipped in the hot dipping bath is kept in the range of 400 to 470 0 C. This is because when the temperature of the steel sheet to be dipped in the hot dipping bath is equal to or lower than the bath WO 89/09844 pCr/jP89/0029.1' temperature and also that of the steel sheet to be pulled out of the bath is lower than the bath temperature, the steel sheet will have a thickness larger than that of the coating layer and, since the temperature of the sheet pulled out is lower than the bath temperature, the cooling of the coating layer is started with the inner face and the Al concentration is high in the surface layer, since Al tends to concentrate in a part which is solidified later. However, when the temperature of the steel sheet is lower by more than 80*C, the adhesion of the coating layer is reduced and the lowering in the bath temperature is serious to thereby increase the operation cost.
The Al concentration in the grain boundaries where solidification occurs later is higher than that in the grain centers where crystallization occurs in an initial stage. In practice, the Al concentration in the surface layer is uneven and it forms a honey-comb pattern in which parts of a relatively low Al concentration are surrounded by parts of a high Al concentration. However, the area of the parts of the high Al concentration is large enough for improving the corrosion resistance of the whole surface.
Although the Al-Zn crystals are formed also in the surface layer upon cooling of the surface layer, also the homogeneous dispersion of Al in the surface layer is accelerated, since the cooling velocity of the whole coating layer is increased by dipping the steel sheet kept at a low temperature. Further the bath is
I
preferably a low temperature bath.
The invention also encompasses a process for producing a hot-dip zinc-aluminum alloy coated steel sheet for a prepainted steel sheet, wherein the steel sheet is taken out of the hot dipping bath and then the amount of the molten zinc-aluminum alloy deposited on the steel sheet is controlled with a gas wiping type of equipment for controlling the amount of the molten zinc-aluminum alloy deposit under conditions comprising a slit clearance of 0.6 to 2.4 mm, a distance between front and back nozzles of to 40 mm and an ejecting pressure of gas of 0.1 to kg/cm 2 in the step of coating in the hot dipping bath.
As described above, the Pb concentration in the hot "dipping bath must be controlled to 100 ppm or g
S
•••oo j WO 89/09844 PCT/JP89/0029 1 less in order to obtain an excellent adhesion after aging.
However, when the Pb concentration is 500 ppm or less, the surface of the coating layer has a ripping pattern to impair the appearance thereof unfavorably. After intensive investigations made for the purpose of eliminating such a pattern from the surface, the inventors have succeeded in obtaining an excellent appearance by controlling the amount of the molten zinc-aluminum alloy deposit with a gas wiping type of equipment under conditions comprising a nozzle slit clearance of 0.6 to 2.4 mm, a distance between front and back nozzles of 10 to 40 mm and an ejecting pressure of gas of 0.1 2 to 2.0 kg/cm These values are limited for the following reasons: 1. Nozzle slit clearance: When the lower limit is less than 0.6 mm, the secondary pressure variation of the gas is too much to obtain a consistent appearance.
When the upper limit exceeds 2.4 mm, the amount of the gas is too much and the energy loss is serious.
2. Distance between front and back nozzles: The lower limit is 10 mm, because when it is less than 10 mm, the vibrating strip is apt to be brought into contact with the nozzle to cause troubles.
The upper limit is 40 mm, because a shorter distance gives a better result and the appearance is S impaired when it exceeds 40 mm.
1 NF -4- WO 89/09844 PCT/JP89/00291 3. Ejecting pressure of gas: 2 The lower limit is 0.1 kg/cm because when it is below 0.1 kg/cm 2 the amount of the deposition cannot be controlled.
2 The upper limit is 2.0 kg/cm because when 2 it exceeds 2.0 kg/cm 2 the energy loss is large and a more consistent appearance can be obtained with a lower pressure.
The control of the amount of the deposition is necessary in order to conform to Z 27 specified in JIS G 3302 or G 90 specified in ASTM A 525.
The invention stated in Clam elates to a process for producing a hot-dip zinc-aluminum alloy coated steel sheet for a prepainted steel sheet .ccording tc Claim 5 Cr 6, wherein the hot-dip zinc-aluminum alloy coated steel sheet is reheated to a temperature above melting temperature of the coating layer.
The reheating temperature is preferably 420°C or higher, because the appearance of the sheet can be improved at such a high temperature.
Although the reheating temperature is preferably 420 0 C or above, a high temperature is not preferred from the viewpoints of both energy and equipment cost. Thus, a temperature in the range of 420 0 C to 560°C is more preferred.
In this invention, the effect similar to that Po bove of -laim 4 can be obtained even when the temperature j of the steel sheet dipped in the hot dipping bath is t ifrh I r higher than that of the hot dipping bath, because the temperature of the steel sheet is lower than that of the coating layer in the step of melting the coating layer surface again and, therefore, the recrystallization of the molten coating metal starts with the side in contact with the steel sheet. The alloy layer formed between the steel sheet and the coating layer is not molten again, because it has a high melting point and, therefore, the Al distribution in the alloy layer is kept unchanged and the adhesion of the coating layer is kept high.
The invention preferably relates to a process for producing a hot-dip zinc-aluminum alloy coated steel sheet f!or a prepainted steel sheet, wherein the hot-dip S zinc-aluminum alloy coated steel sheet is cooled to the solidifying point thereof at a rate of at least 10 0 C/sec.
S
The lower limit of the cooling rate is because stable corrosion resistance can be obtained at a cooling rate of at least 10 0 C/sec. Although the higher limit thereof is not limited, a cooling rate of 150 0 C/sec or less is desirable from the viewpoints of the energy cost and equipment.
The invention suitably relates to a prepainted steel sheet having excellent workability and corrosion resistance which comprises the hot-dip zinc-aluminum alloy coated steel sheet produced according to the process of the present invention, a layer formed thereon by chemical /XiV\ conversion treatment and further a surface painting film 21 layer formed thereon.
The surface painting film layer comprises those of one-coat, two-coat, three-coat, four-coat type, etc.
Usually, a two-coat layer is used.
The present invention will be described in detail withreference to a two-coat surface painting film layer.
First, an under-painting paint is applied to the sheet and baked.
The sheet used is the hot-dip zinc-aluminum alloy coated steel sheet. The sheet may have a layer formed by chemical conversion treatment having a thickness of about 0.1 to 5 The chemical conversion treatment is conducted in S"order to improve the corrosion resistance of the sheet and coo• the adhesion of the paint to the steel sheet. The chemical conversion treatments include, for example, a treatment e with a phosphate such as zinc phosphate, iron phosphate, manganese phosphate or cobalt phosphate, and a treatment oe with a chromate such as electrolytic chromate treatment and S. applied chromate treatment.
As the under-painting paints, those ordinarily used for the production of prepainted steel sheets can be used.
They include, for example, paints prepared by mixing coloring pigment, rustproof pigment, body, IrC- Mil PC/JP89/00291 WO 89/09844 etc. in a resin solution mainly comprising a resin such as epoxy, oil-free polyester, acrylic or urethane resin.
Among them, an under-painting paint mainly comprising the epoxy resin which has excellent adhesion and corrosi in resistance or the oil-free polyester resin which has also a good workability is preferred. The thickness of the under-paint is 1 to 15 p, preferably 2 to 12 p, because the corrosion resistance and scratch resistance are further improved with a thickness of at least 2 p and the workability is further improved with that of 12 p or less. When the thickness exceeds 12 p, the cost is increased, The rustproof pigment may contain 5 to of at least one of strontium chromate, zinc chromate, red lead, zinc plumbate, calcium plumbate, lead cyanamide, basic lead chromate, basic lead silicochromate, basic zinc molybdate and calcium zinc molybdate depending on the use and environments. With at least 5% of this pigment, the rust formation in an early stage can be completely inhibited and no blister is formed with or less thereof.
After formation of the under-paint, a top-paint paint is applied thereto and baked to form a topcoat.
The top-painting paint comprises preferably acrylic resin, oil-free polyester resin, silicone polyester resin, silicone acrylic resin, alkyd resin, polyurethane resin, polyimide resin, polyamide resin, fluororesin or the like. The thickness of the top-paint is 8 to 50 p, -8 I EWA&-ia WO 89/09844 PCT/JP89/00291 preferably 10 to 45 p, because the scratch resistance, workability and weather resistance are improved with the thickness of at least 10 p but the cost is increased when the thickness is beyond 45 p.
When the Pb concentration exceeds 100 ppm, the adhesion after aging is reduced due to intercrystalline corrosion and, as a result, the corrosion resistance of a worked part which is important particularly in the prepainted steel sheet is also reduced. The concentrations of Al and Pb must be thus limited in order to produce the prepainted steel sheet having excellent properties.
p rereb V-I The invention stated in Glaim 10relates to a prepainted steel sheet a eording to Cl-ai 9, wherein the chemical conversion layer is one formed by treating the sheet with a chromic acid solution containing silica having an average particle diameter of 50 mp and specific surface area of 200 m /g in such a manner that the amount of the coating film after drying will be 50 to 250 mg/m 2 to impart an excellent scratch resistance.
In the invention -ctatd in Claim 10, the chromic acid solution containing silica having an average particle diameter of 50 mp is used. The smaller the average particle diameter of silica, the better the workability and adhesion, though the scratch resistance is not improved when the average particle diameter is too small.
When the average particle diameter is too large, the particles are liable to be precipitated disadvantageously.
I-.l WO 89/09844 PCT/JP89/00291 In this invention, the specific surface area of silica in the chromic acid solution is 200 m /g.
Although it varies depending on the average particle diameter, no scratch resistance can be obtained when the specific surface area is excessively small.
The chemically converted layer is formed with the above-described chromic acid solution in such a manner that the amount of the coating film after drying will be 50 to 250 mg/m 2 With at least 50 mg/m 2 of the film after drying, both the scratch and corrosion resistances are improved and with 250 mg/m 2 or less thereof, the workability, adhesion and scratch resistance are improved.
(Examples) The following Examples will further illustrate the present invention.
The materials to be coated were low-carbon aluminum killed steel sheets (0.8 mm x 914 mm x coil) in all the cases. The sheets were hot-dip coated with Zn-Al alloy with Sendzimir continuous zinc coating equipment.
The invention s-tated in Claim I rf -i-h pre-sen aplication will be described with reference to Examples.
Example 1 Hot-dip zinc-aluminum alloy coated steel sheets were produced with hot dipping baths having various Al concentrations and the workability thereof was examined in order to confirm the effects obtained by the addition /I l of Al according to the present invention.
WO 89/09844 PCT/JP89/00291 The conditions were as follows: sheet thickness: 0.8 mm bath temperature: 460°C dipping time in the bath: 4 sec amount of deposition: 120 to 260 g/m 2 Pb concentration: 50 ppm Test method: The OT and 2T bending test methods according to JIS G 3312 were employed. The term "OT bend" and "2T bend" refer to the bends realized when a steel sheet having a thickness of the base metal of T is bend with a hand vise or other suitable means to give an inner diameter of the bend of OT and 2T, respectively. The cracks of the coating layer in the bend part were examined and the results were classified inio five groups. The standard is shown in Table 1 and the results are shown in Table 2.
Table 1 (Standard of evaluating degree of cracking) Standard No crack formed.
4 Extremely slight crack formation observed.
3 Slight crack formation observed.
2 Crack formation distinct.
1 Crack formation remarkable.
e WO 89/0984 4 PCT/J P89/0029,1 Table 2 Workability Al. Wt% 0OT 2 T 0 arative 0 1, 12 0 .2 23 0 .3 3 4 0 .5 1 .0 4.5 1.54.5 ,ent__ .ntion 2 .0 4 3 .055 3 .555 .0 parative, .0 34 .0 2 3 The numerals in-.Table 2 are the -averages of the results.
L
i I WO 89/09844 PC/JP89/00291 Example 2 Hot-dip zinc-aluminum alloy coated steel sheets were produced with hot dipping baths having various Pb concentrations and the prolonged adhesion thereof was examined in order to confirm the effects of Pb added according to the present invention.
The conditions were as follows: sheet thickness: 0.8 mm bath temperature: 460 0
C
dipping time in the bath: 4 sec amount of deposition: 120 to 260 g/m 2 Test method (adhesion after aging or adhesion after working: A paint was applied to the test pieces in a thickness of about 5 p and then baked in order to prevent formation of white rust. The test pieces were immersed in hot water kept at 80 0 C for 3 days and taken out.
The painting film was removed with a stripping agent.
A semi-spherical steel mass weighing 5 kg and having a radius of 3/4 inch was dropped from a height of 500 mm.
An adhesive tape was applied to the projecting coated surface to forcedly strip it to thus determine the adhesion of the coating layer. The standard is shown in Table 3 and the results are shown in Table 4.
WO 89/09844 PCT/JP89/00291 Table 3 (Standard of adhesion after aging or adhesion after, working) Standard No peeling observed.
4 Extremely slight peeling observed.
3 Slight peeling observed.
2 Peeling distinct.
1 Peeling remarkable.
W/O 89/09844 89/09844PCT/J P89/00291 Table 4 Adhesion after aging P b p pm) Al2 wt% 0 50 100 200 300 500 1000 0 5 5 5 5 5 5 0.1 5 5 5 4 4 4 4 0.2 5 5 5 3 2 1 1 0.3 15 5 5 3 2 1 1 5 5 5 2 1 1 1 5 5 5 1 1 1 1 1 .5 5 5 5 1 1 1 1 2 .0 5 5 5 1 1 1 1 2 .5 5 5 5 1 1 1 1 5 5 5 1 1 1 1 3 .5 5 5 5 1 1 1 1 5 5 5 1 1 1 1 5 5 5 1 1 1 1 .The hot balance dipping of Zn.
bath comprised Al, Pb and the The numerals in Table 4 are the averages of the re~ults.
I .r WO 89/09844 PCT/JP89/00291 .Th f 1- .wing FYm-Uu...pl.. the- 3 F invention stated in Claim 2 of the present appiciation.
Example 3 Hot-dip zinc-aluminum alloy coated steel sheets were produced with hot dipping baths containing various amounts of Si and the workability and adhesion thereof were examined in order to confirm the effects obtained by the addition of Si according to the present invention.
(Test method) A semi-spherical steel mass weighing 5 kg and having a radius of 3/4 inch was dropped from a height of 500 mm and an adhesive tape was applied to the projecting coated surface to forcedly strip it to thus determine the adhesion of the coating layer. The results are shown in Table 5. The standard is the same as that shown in Table 3.
The conditions were as follows: sheet thickness: 0.8 mm bath temperature: 460°C dipping time in the bath: 4 sec amount of deposition: 120 to 260 g/m 2 Pb concentration: 50 ppm In Table 5, the results of OT crack formation according to the bending test are shown in the upper row and those of OT tape tests on adhesion after working are shown in the lower row.
When the Al concentration is in the range of 0.3 to 3.5 wt.% and the Pb concentration is not higher WO 89/09844 PCT/J P89/00291 r 3" than 100 ppm, hot-dip zinc-aluminum alloy coated steel sheets having excellent workability and adhesion after aging can be obtained. It is preferred, however, to add 1/100 to 1 part of Si per part of Al to control the formation of the alloy layer and, therefore, to form only a thin alloy layer. By this process, a hot-dip zinc-aluminum coated steel sheet further improved in adhesion after aging can be obtained. When only 1/200 part cf Si is added per part of Al, no improvement is observed.
It was thus confirmed that when the Al concentration was 0.3 to 3.5 Pb concentration was 100 ppm or less and Si concentration was 1/100 to 1 part per part of Al, an intended hot-dip zinc-aluminum alloy coated steel sheet which has excellent workability and adhesion can be obtained.
Table 0 A0 Bathraiv 0o.oito Alti of Si X o Al3 S X 0. Al X 4 3 4 3 3 -7 X- Copraie0.3 A2 r X X 4 4 5 5 5 5 5 4 X5 4 5 5 5 5 Al 5 Present
Z
invention X 5X 5X X Al! 5X 5X 5IX X 2 .0 Al!. 3. 25 5 5 5 5 5 Comparative 5.0 A! 00 The numerals of the evaluation results in Table 5 are the averages of the results. (Z
W
~II_ i ':WO 89/09844 PC~/JP9/00291 S,33 .Th fnllnwing yamp-P d jI4 wll ill 'strat th---e invention stated i.n Claim I of thc prcnt applicaftion.
Example 4 Hot-dip zinc-aluminum alloy coated steel sheets were produced with hot dipping baths containing various amounts of Mg, Mn or Cu and the corrosion resistance and adhesion after aging thereof were examined in order to confirm the effects obtained by the addition of it.
The conditions were as follows: sheet thickness: 0.8 mm bath temperature: 460°C dipping time in the bath: 4 sec amount of deposition: 120 to 260 g/m 2 Pb concentration: 50 ppm (Test method) Test pieces prepared under the conditions shown in Table 7 were subjected to the chromate treatment.
An epoxy resin under-paint having a thickness of 5 P and then a silicone polyester resin top-paint having a thickness of 15 p were formed. After baking, they were subjected to a salt spray test according to JIS Z 2371 and the corrosion resistance in the OT part of each of the prepainted steel sheets was examined. The results are shown in Table 7. The standard is shown in Table 6.
PAT
1( ^7~L~ i I i I 1 WO 89/09844 PCT/JP89/00291 Table 6 (Standard of evaluation of corrosion resistance) Standard No white rust formed.
4 Extremely slight white rust formation observed.
3 Slight white rust formation observed.
2 White rust formation distinct.
1 White rust formation remarkable.
The adhesion after aging was tested in the same manner as that of Example 2 and the results were evaluated according to the standard shown in Table 3.
When a metallic element such as Mg, Mn or Cu capable of improving the corrosion resistance of the galvanized steel sheet was added to the hot dipping bath, the effect of the present invention could be further improved. The effective concentration of the metallic element was 0.01 wt.% or higher. A combination of Si with Mg, Mn or Cu is also usable. By controlling the Pb concentration below 100 ppm, a stable adhesion after aging could be obtained.
I U I Table 7 Corrosion resistance OT part Adhesion Composition of deposit SST (1000 Hr) after aging Si 0 Si 1/1* Comparative 0.3 Al-0.02 Pb-balance Zn 3 4 3 0.3 Al-0.005 Pb-balance Zn 3 4 0.3 Al-O.005 Pb-0.0l Mg-balance Zn 5 5 0.3 Al-0.005 Pb-0.03 Mg-balance Zn 5 5 0.3 Al-0.005 Pb-l.0 Mg-balance Zn 5 5 0.3 A1-0.005 Pb-1.5 Mg-balance Zn 5 5 Peet 0.3 Al-0.005 Pb-0.0l Mn-balance Zn 4 5 Preentio 0.3 Ai-O.005 Pb-0.02 Mn-balance Zn 5 5 ivnin 0.3 Al-O.005 Pb-l.2 Mn-balance Zn 5 5 0.3 Al-0.,005 Pb-l.5 Mn-balance Zn 5 5 0.3 Al-0.005 Pb-0.0l Cu-balance Zn 4 4 0.3 Al-0.005 Pb-0.04 Cu-balance Zn 4 5 0.3 Al-0.005 Pb-0.08 Cu-balance Zn 4 5 0.3 Al-0.00S Pb-1.5 Cu-balance Zn 5 5 Comparative 0.5 Al-0.03 Pb-balance Zn 3 4 1 Al-0.005 Pb-balance Zn 3 4 5 Al-0.005 Pb-0.0l Mg-balance Zn 5 5 Al-0.005 Pb-0.02 Mg-balance Zn 5 5 Al-O.005 Pb-0.09 Mg-balance Zn 5 5 1.1-0.005 Pb-l.5 Mg-balance Zn 5 5 Peet 0.5 1.1-0.005 Pb-0.0l Mn-balance Zn 5 5 Preento 0.5 1.1-0.005 Pb-0.03 Mn-balance Zn 5 5 ivnin 0.5 1.1-0.005 Pb-1.l Mn-balance Zn5 1.1-0.005 Pb-l.5 Mn-balance Zn 5 5 AL-0.005 Pb-0.0l Cu-balance Zn 5 1.1-0.005 Pb-0.03 Cu-balance Zn 5 1 0.51-0.005 Pb-0.09 Cu-balance Zn 5 I 5 0.51-0.005 Pb-l.5 Cu-balance Zn 5 j 5 Amount of Si was I part per part of Al, The numerals of the evaluation results in Table 7 are the averages of the results.
0 Ge '0 '0 00 WO 89/09844 PCT/JP89/00291 The following Example 5 will illustrate the .invCntion ctated in Claim 4 of the prcccnt applicatien.
Example Hot-dip zinc-aluminum alloy coated steel sheets were produced at various steel sheet temperatures and hot dipping bath temperatures as shown in Table 10 and the workability and corrosion resistance thereof were examined in order to confirm the effects of the present invention.
The results are shown in Table In this example, the temperature difference between the steel sheet and the bath was controlled to be 0 to 80 0 C to reduce the energy required to maintain the bath temperature.
(Test methods) Surface corrosion resistance test The four edges of each of the test pieces having a size of 60 mm x 60 mm were sealed by coating. Further the whole surface of the test piece other than the surface to be tested was also sealed by painting and then dried.
The painting was conducted in such a manner that the area of the exposed surface of the test piece would be mm x 50 mm. Then the test piece was thrown into a salt spray testing instrument and tested according to JIS Z 2371. After the completion of the test conducted for 100 Hr., the test piece was taken out, corrosion w products were removed from the exposed surface thereof and the test piece was weighed. The loss due to corrosion
J
i.nh v/ WO 89/09844 PCT/JP89/00291 (g/m 2 was determined by dividing the difference in weight between that before the test and that after the test with the area of the test surface. Th standard is shown in Table 8.
-7 Table 8 (Standard of evaluation of surface corrosion resistance) Standard Loss due to corrosion 50 g/m 2 or less 4 Loss due to corrosion 50 g 75 g/m 2 3 Loss due to corrosion 76 100 g/m 2 2 Loss due to corrosion 101 125 g/m 2 1 Loss due to corrosion 126 g/m 2 or above Initial red rust test on edge The test piece was placed in a salt spray testing instrument for 160 Hr. and red rust formed on the edges thereof was examined. The salt spray test was conducted according to JIS Z 2371. The standard of the examination of the red rust is shown in Table 9.
.I.
WO 89/09844 PCT/JP89/00291 Table 9 (Standard of examination of initial red rust formed'on edge) Standard No red rust formed.
4 Extremely slight red rust formation observed.
3 Slight red rust formation observed.
2 Red rust formation distinct.
1 Red rust formation remarkable.
The lower is the temperature of the steel sheet at the time of dipping into the bath, as compared with the bath temperature, the better is the corrosion resistance. The temperature difference between the sheet and the bath is preferably within 80°C to reduce the energy require, to maintain the bath temperature.
The Al distribution on the coating layer surface -K-rn P e-4r- Z 0 C-Q_ at various steel sheet tetmperatus at dipping time is shown in Figs. 1. The samples used for the determination of this distribution were prepared under the following conditions: bath composition: 1 wt.% of Al, 0.005 wt.% of Pb, 0.02 wt.% of Si and the balance of Zn sheet thickness: 0.8 mm bath temperature: 460°C dipping time in the bath: 4 sec Figs. 1(b) and l(c) are microphotographs WO 89/09844 PCT/JP89/00291 of the metal textures obtained when (steel plate temperature at dipping time) (bath temperature) was -20°C and -80°C, respectively.
The Al distribution was determined with EPMA (EMX-SM 7; a product of Shimadzu Seisakusho Ltd.).
Fig. 2(b) shows the distributions of Fe, Zn and Al in the cross section of the hot-dip Zn-Al alloy coated steel sheet. This figure substantiates the fact that Al in the coating layer was distributed on the surface layer thereof to improve the corrosion resistance.
Fig. 2(a} shows a cross section of the coating layer of a hot-dip Zn-Al alloy coated steel sheet proiuced by a conventional process. It is apparent that Al is distributed densely in the alloy layer.
It is thus apparent from the above figures that Al is distributed mostly in the surface layer of the coating layer in the products of the present invention unlike the products produced by a conventional process.
As described above, the present invention provides a hot-dip Zn-Al alloy coated steel sheet which has an excellent corrosion resistance of the coating layer, which is prevented from the initial red rust formation on the edges of the sheet and which has an excellent workability of the coating layer.
j 4Y 00 Table Steel (Steel 2Hot dipping bath composition sheet sheet Amsount Corrosion Corrosion Cwt.1) Bath temp. temp. at ot Workability resistance resistance temp. at d ipping deposi- (2T bending (SST 100 Hir) (SST 160 Hir) dipping time) tion with vise) l b S ntime (Bath (gin 2 Surface Initial red Pb S temp,)(OC) .rust on edge 0.56 0.005 0 balance 480 420 -40 112 5 4 0. 005 0. 1 balance 460o 420 -40 108 5 5 0.005 0 balance 480 400 -80 113 5 5 invention. 1.0 0*.005 0 balance 480 440 -40 115 5 2 .0 0. 005 0 balance 460 440 -20 107 5 5 2 .0 0. 005 0 balance 460 420 -40. 116 5 0. 005 0.1 balance 460 4 20 -40 110 5 5 Comparative 0.2 0.005 0 balance 460 480 +20 110' 3 2 Present 0.5 0. 005 0 balance 460 465 5 109 invention.34 fresen 1.0 0.005 0 balance 480 485 5 108 5 3 4 Comparative 50 0Ob 0 balanc 6 47.0 +10 11'0 E; 5 3 L The numerals of the evaluation results in Table 10 are the averages of the results.
"V
00
I
WO89/09844 PCT/JP89/00291
A.
'Thc following Ecample 6 w-ill illustrate the 'invention statd- in Claim 5 of the preent ftliYcP itrL.
Example 6 The steel sheet was pulled out of the hot dipping bath and the surface smoothness of the sheet was improved by means of a gas wiping type of equipment for controlling the amount of zinc deposit under conditions comprising a slit clearance of 0.6 to 2.4 mm, a distance between front and back nozzles of 10 to 40 mm and an ejecting of 0.1 to 2.0 kg/cm The appearance (smoothness of the coating layer surface) of the produced hot-dip zinc-aluminum alloy coated steel sheet was examined.
The conditions were as follows: line speed: 100 m/min sheet thickness: 0.8 mm bath composition: 1 wt.% of Al, 0.005 wt.% of Pb, 0.02 wt.% of Si and the balance of Zn bath temperature: 460 0
C
dipping time in the bath: 4 sec Fig. 3 is a schematic drawing of the hot dipping equipment having a gas wiping type of means for controlling the amount of zinc deposit used in this, Example.
(Test method) The appearance (smoothness) of the coating layer surface was evaluated on the basis of the standard WO 89/09844 PCT/JP89/00291
-S
4shown in Table 11. The results are shown ir Tables 12(1) and 12(2).
Table 11 (Standard of evaluation of appearance smoothness of coating layer surface) Standard No ripple observed.
4 Extremely slight ripples observed.
3 Slight ripples observed.
2 Ripples distinct.
1 Ripples remarkable.
Although the Pb concentration in the bath must be controlled to be 100 ppm or less to obtain an excellent adhesion after aging as described above, a Pb concentration of 500 ppm or less is not preferred for obtaining a good appearance, because a rough ripply pattern is formed on the surface with a Pb concentration of 500 ppm or less.
It is apparent from Tables 12(1) and 12(2) that a good appearance (smoothness) can be obtained by the invention stated in Claim 5 of the present application.
The control of the amount of the deposition is necessary in order to conform to Z 27 of JIS G 3302 or G90 of ASTM.A525. The control thereof in the range f 50 t 400 /m 2 is easy in of 50 to 400 g/m is easy in Example 6.
4k' t WO 89/09844 Upper row: Lower row: PCT/JP89/00291 Table 12(1) appearance (smoothness of the coating layer surface) Possibility of control of the amount of deposition The numerals of -the evaluation results in Table 12(1) are the averages of the results.
WO 89/09844 PCT/J P89/002? 1 Table 12(2) The numerals of the -evaluationx results in Table 12 (2) are the averages--of the results.
C~
WO -89/09844 PCT/JP89/00291 -4- IrV,_ F- I I L" nm I 7 1 1 4 1 1 CL- 1- .nir c r4-+lA 4. C ZUL~LLULZ LII~ t-.
.ZX~FrJ~ LfrJfrJ 4.A4 S* Example 7 ~I~IU- .Y -F~I~PI~~ZIIZ Urr-I ~~LL CIVII The steel sheet was pulled out of the hot dipping bath and treated with a gas wiping type of equipment for controlling the amount of zinc deposit under conditions comprising a slit clearance of 0.6 to 2.4 mm, a distance between front and back nozzles of to 40 mm and a gas ejecting pressure of 0.1 to kg/cm 2 to give a hot-dip zinc-aluminum alloy coated steel sheet. The appearance (surface smoothness) of the sheet was examined.
The conditions were as follows: sheet thickness: 0.8 mm bath temperature: 460°C dipping time in the bath: 4 sec amount of deposition: 250 g/m 2 bath composition: 0.5 wt.% of Al, 0.005 wt.% of Pb, 0.01 wt.% of Si and the balance of Zn (Test method) The appearance (smoothness) of the coating layer surface was evaluated on the basis of the standard shown in Table 11. The results are shown in Table 13.
WO 89/09844 WO 8909844PCT/J P89/00291 Table 13 (Bath temp. Distance (Steel. Slit Gas between Surface. Control of sheet clear- ejecting front smoh amuto temp. at, ance pressure and back' ness deposition dipping (mm) (kg/cm 2 nozzle time)(*C) (mm) Comparative 1-20 0.4 1.0 20 2 possib'le 0.6 1.5 20 3 possible 1.2 2.0 40 4.5 possible 2.0 1.5 10 4.5 possible Presento ivnin -60 2.4 0.1 30 5 possible 1.2 0.1 20 5 possible 2.4 2.0 10 5 possible mparative -60 0.8 1.0 50 1 impossible The numerals of the -smoothness in Table 13 are the averages of the results.
A.
WO 89/09844 PCT/JP89/00291 1+-7 Figs. 4(a) to show the appearances of the sheets produced in this Example and Comparative Example.
Fig. 4(a)-is microphotograph of a sheet produced under conditions comprising (steel sheet temperature at dipping time) (bath temperature) of -60°C, a nozzle slit clearance of 0.8 mm, a gas ejecting pressure of 2 kg/cm and a distance between front and back nozzles of 50 mm (the result of the evaluation of the appearance: Fig. 4(b) is that produced under conditions comprising (steel sheet temperature at dipping time) (bath temperature) of -20 0 C, a nozzle slit clearance of 0.6 mm, a gas ejecting pressure of 1.5 kg/cm 2 and distance between front and back nozzles of 20 mm (the result of the evaluation of the appearance: 3).
Fig. 4(c) is that produced under conditions comprising (steel sheet temperature at dipping time) (bath temperature) of -80 0 C, a nozzle slit clearance of 1.2 mm, 2 a gas ejecting pressure of 0.1 kg/cm 2 and a distance between front and back nozzles of 20 mm (the result of the evaluation of the appearance: By the process statod in Claim 6. a hot-dip zinc-aluminum alloy coated steel sheet having excellent appearance and corrosion resistance and being suitable for use as a material for prepainted steel sheet could be obtained.
The following XFvAmpIp will iLj.1ls-rat-p the -nvFnte+, gqtrtad A S1 an~ he l u tn r.
WO 89/09844 PCr/JP89/00291 Example 8 The hot-dip zinc-aluminum alloy coated steel ervCl% I or 7 sheet produced by the process of Slaim as reheated to various temperatures shown in Table 14 which were above the melting temperature of the coating layer in order to make its surface smooth. The appearance (smoothness), thickness of the coating layer and Al distribution in the obtained hot-dip zinc-aluminum alloy coated steel sheet suitable for use as a material for a prepainted steel sheet were examined.
The conditions were as follows: sheet thickness: 0.8 mm bath temperature: 460°C dipping time in the bath: 4 sec amount of deposition: 250 g/m 2 bath composition: 0.5 wt.% of Al, 0.005 wt.% of Pb, -0.01 wt.% of Si and the balance of Zn The standard of the evaluation of the appearance (smoothness) of the coating layer surface is shown in Table 11 and the results thereof are shown in Table 14.
I
SWO 89/09844 PCr/JP89/00291 Table 14 Reheating temp. Smoothness of 0 C) coating layer surface not reheated 3 Comparative 380 3 400 3 420 4 Present 460 invention 500 560 The numerals of the evaluation results are the averages of the results.
The surface smoothness was remarkably improved at a reheating temperature of 420'C or above.
The results of the determination of the thicknesses of the coating layers obtained without any reheating and with the reheating at 460°C are shown in Figs. It is apparent from Figs. 5 that the scattering in the thickness of the coating layer was narrow when the reheating was conducted according to the present invention. The scattering of the thickness of the coating layer was closely related to the appearance. Namely, the narrower the scattering, the less the formation of the ripples.
The thickness of the coating layer was determined with a micro-fluorescence X-ray device
-I
I
WO 89/09844 PCT/JP89/00291 (SPT-157 SLS; a product of Seiko Denshi Co., Ltd.) with a beam diameter of 0.1 mm.
The distribution of Al atoms, etc. was examined with ESCA. The distribution of Fe, Zn and Al in the cross section of the coating layer on the hot-dip An-Al alloy coated steel sheet is shown in Table 15. The results support the fact that Al is distributed in the surface layer of the coating layer and the coated steel sheet of the present invention has an excellent corrosion resistance.
The conditions were as follows: sheet thickness: 0.8 mm bath temperature: 460°C dipping time in the bath: 4 sec amount of deposition: 250 g/m 2 bath composition: 1 wt.% of Al, 0.003 wt.% of Pb, 0.01 wt.% of Si and the balance of Zn The ESCA instrument used was JPS-90 SX of JEOL, Ltd. The acceleration voltage was 500 and the etching rate was 250 A/min (in terms of SiO 2 (the etching rate of Zn is about 4 times as high as that of SiO2).
i WO 89/09844 1 PCT/JP89/00291 Table 15 (Atomic distribution change with depth from surface layer) (Atomic (Atomic (Atomic (Atomic 1 Depth D Zn 0- C A 0 3.21 40.58 38.95 17.25 33A 5.62 57.94 8,17 28.25 200A 13.62 53.27 7.76 25.33 Surface layer layer 1200A 95.11 1.97 0.86 2.04 6200 A 98.18 1.13 0.30 0.37 11200A 97.85 0.70 0.99 0.44 *The following Example 9 will illustrate tho invention ctated in Claim 0 of the preseint pliUcLtiuii.
Example 9 Hot-dip zinc-aluminum alloy coated steel sheets were produced at various cooling speeds as shown in Table 16 in order to obtain a stable corrosion resistance.
The workability and corrosion resistance of the sheets were examined.
The conditions were as follows: sheet thickness: 0.8 mm bath temperature: 460°C dipping time in the bath: 4 sec amount of deposition: 120 to 260 g/m A CIr il ux;; WO 89/09844 PCT/JP89/00291 bath composition: 1 wt.% of Al, 0.005 wt.% of Pb, 0.01 wt.% of Si and the balance of Zn The workability test was conducted in the same manner as that of Example 1 and the results were evaluated on the basis of the standard shown in Table 1.
In the corrosion resistance test, the initial red rust formation in the edges was examined in the same manner as that of Example 5 and the results were evaluated on the basis of the standard shown in Table 9.
Table 16 Corrosion Cooling speed Workability' resistance C/sec) 2T (red rust on edge) SST 160 Hr Comparative 5 5 3 5 4 Present 20 5 4 invention 5 5 The numerals of the evaluation results are the averages of the results.
C\
WO 89/09844 i'CT/JP89/00291 It is apparent that the corrosion resistance was improved when the cooling was conducted at a speed of at least 10°C/sec after the hot dipping.
Figs. 6(a) to are microphotographs showing the metal textures of the coating layer surfaces. They are X-ray images of Al on the surfaces formed with EPMA.
Figs. 6(b) and 6(c) are microphotographs of the metal textures of the coating layer surfaces obtained when the cooling speed was 2 0 C/sec, 17°C/sec and 47°C/sec, respectively.
It is apparent from Figs. 6(a) to that as the cooling speed was increased, the Al distribution on the coating layer surface became homogeneous and Al concentrated in the surface layer.
The fo!!owing ExaU-l ii to 19 will iiiu±ctit"e the invention in Claim 9 of the present Example 11 Hot-dip zinc-aluminum alloy coated steel sheets were produced with baths containing various amounts of Al and Pb in order to confirm the effects of Al and Pb added to the bath according to the present invention (Example Each of them was used as the material sheet.
It was treated with a chromate. An epoxy resin paint containing 15% of a rustproof pigment was applied thereto.
After baking at 210 0 C for 35 sec, an under-paint having a dry thickness of 3 p was given. Then an oil-free polyester resin paint as the top-painting paint was II:" 'I i i WO 89/09844 PCT/JP89/0O021 applied thereto and baked at 220 0 C for 45 sec to form a top-paint having a dry thickness of 11 i.
The properties of the prepainted steel sheets thus prepared were examined. The results are shown in Table 17.
The workability was determined by the same 2T bending test method as that of Example 1 and the results were evaluated on the basis of the standard shown in Table 1.
The adhesion was determined also in the same manner as that of Example 1. Namely, after the 2T bending test, an adhesive tape was applied to the 2T part of the prepainted steel sheet and the forced stripping test was ccnducted. The results were evaluated on the basis of the standard shown in Table 3.
The corrosion resistance test was conducted according to JIS Z 2371 in the same manner as that of Example 4. The flat part and 2T part were subjected to the salt spray test (SST, 1000 The results were evaluated on the basis of the standard shown in TabLe 6.
The workability, adhesion and corrosion resistance were determined immediately after the preparation of the prepainted steel sheets and after six months.
When the Al concentration was in the range of 0.3 to 3.5 the prepainted steel sheets having excellent properties could be obtained.
L
WO 89/09844 PCT/JP89/00291 When the Pb concentration exceeded 100 ppm, the workability, adhesion and corrosion resistance were reduced with the elapse of time.
Table 17 Corrosion resistance Bath composition Workability Adhesion SST 1000 Hr 2Tfltpr2Tat imznedi- immnedi- ___Iimied iately after atelY af ter a e afte a fe atr 6 after 6 V a aeryafe 6. Pb Zi_ 6rdc months tion mots tion months t on~ months tion -months Comparative 0.1 0.01 balance 3 3 5 5 5 5 3 3 0.3 0.005 balance 4.5 4.5 5 5 5 5 4.5 invention 100 0.005 balance 5 5 5 5 5 0.01 balance 55 5 5 5 5 0.005 balance 5 5 5 5 5 55 0.1 0.02 balance 3 2.5 5 4 5 4 3 0.3 0.03 balance 4.5 2 5 2 5 2 1 4.5 2 Comparative 1 0 0 0 a a c 0.03 balance 5 1 5 1 5 1 5 1 .02 alace 5 1 5 1 5 0'.02 balance 5 1 5 1 5 1 5 1
XT\
The numerals of the evaludtion results are the averages of the results.
WO 89/09844 PCT/JP89/00291 Example 12 Hot-dip zinc-aluminum alloy coated steel sheets were prepared with hot dipping baths containing various amounts of Si in order to confirm the effect of Si added to the bath according to the present invention (Example Each of them was used as the material sheet.
It was treated with a chromate in the same manner as that of Example 11. An under-paint and then a top-paint were formed thereon to prepare a prepainted steel sheet in the same manner as that of Example 11. The workability, adhesion and corrosion resistance of the prepainted steel sheet were determined in the same manner as that of Example 11. The conditions and the results are shown in Table 18.
i PCr/JP89/00291 WO 89/09844 Table 18 Corrosion Bath composition resistance Work- Adhe- SST 1000 Hr ability sion i2T 2T Al Si/Al Pb Zn flat. Tpr part2Tpr 0 1.5 5 5 Comparative 0.1 1 /10 2.5 5 5 1 /1 3.5 5 5 Present 1/ 100 4.5. 5 5 invention 0.3 1 /5 4.5 5 5 Comparative 2 /1 0.005 balance 4.5 5 5 1/ 200 5 5 5 Presen .t 1.0 1/50 5 5 5 invention 1/ 5_ 5 5 Comparative 0 5 5 5 Present 3.5 1 10 5 5 5 invention1/55 5 1100 5 5 5 Comparative 5.0 1/5 5 1 1 2 /i1 5 51 The numerals of the averages of the results.
evaluation results are the WO 89/09844 PC/JP89/00291 Example 13 Hot-dip zinc-aluminum alloy coated steel sheets were prepared with hot dipping baths containing various amounts of Mg, Mn or Cu in order to confirm the effect of them added to the bath according to the present invention (Example Each of them was used as the material sheet. It was treated with a chromate. An epoxy resin paint containing 15% of a rustproof pigment was applied thereto. After baking at 210'C for 35 sec, an under-paint having a dry thickness of 3 p was given.
Then an oil-free polyester resin paint as the top-painting paint was applied thereto and taked at 220°C for 45 sec to form a top-paint having a dry thickness of 11 1.
The workability, adhesion and corrosion resistance of the prepainted steel sheets were determined.
The conditions and the results are shown in Table 19.
The workability was determined by the 2T bending test in the same manner as that of Example 1 and the results were evaluated on the basis of the standard shown in Table 1.
The adhesion in the 2T part of the prepainted steel sheet was determined also in the same manner as that of Example 11 and the results were evaluated on the basis of the standard shown in Table 3.
The corrosion resistance test was conducted according to JIS Z 2371 in the same manner as that of Example 4. The flat part and 2T part were subjected to the salt spray test (SST, 1000 The results "-ki"rlV a ''j ihY d r 8 ~--r~rbc WO 89/09844 PCT/JP89/00291 Ko were evaluated on the basis of the standard shown in Table 6.
It is apparent from Table 19 that when 0.01 to 1.5 wt.% of one or more of Mg, Mn and Cu was(were) added to the bath, the workability, adhesion and corrosion resistance of the prepainted steel sheet were further improved.
tij 1W i 4? 'WO 89/09844 WO 8909844PCT/JP89/00291 Table 19 Corrosion Bath composition resistance Work- Adhe- SST 1000 Hr abilit sion 2T 2T Pb Si Mg, Mn flat ar and Cu npat ZTpr Comparative 0 4*.5 5 5 0.0199 5 .5 0.034g 5 5 5 S Z 5 0.011(n 5 5 Present invention 0.3 0.005 0.3 0.029n balance 5 5 5 1.2 Un 5 5 0.0lCU 5 5 0.04CU 5 5 5 0.08CU 5 5 5 5 Coparative 0 4.5 5 5 0.01Mg 5 5 5 0.02Mg 5 5 5 Yg 5 5 5 0.019n 5* 5 5 Presenit ivnin 0.5 0.005 0.5 0.031(n balance 5 5 5 1.1'Mn 5 5 5 1. 5 n 5 5 5 0.0ICu 5 15 5 0.03CU 5 5 5 0OCu 5 5 5 Cu 5 S S The numerals of the evaluation results are the averages of the results.
WO 89/09844 PCT/JP89/00291
G
Example 14 Hot-dip zinc-aluminum alloy coated steel sheets were prepared by the process stated in Claim 51in which the slit clearance and the distance between front and back nozzles of the gas wiping type of deposit control equipment were varied. The sheets were painted and baked in the same manner as that of Example 12 to form prepainted steel sheets. The surface smoothness of these sheets was determined on the basis of the standard shown in Table 11 in the same manner as that of Example 6.
The conditions and the results are shown in Table The conditions were as follows: bath composition: Al concentration 1.0 wt.% Pb concentration 0.005 wt.% Si concentration 0.02 wt.% Zn concentration the balance According to the present invention, the prepainted steel sheet having a good surface smoothness could be obtained.
t W O 89/09844 PCT/JP89/00291 Table Table Smoothness after coating Slit Gas clear- ejecting ance pressure (mm) (kg/cm 2 Distance between front and back nozzles (mm) 40 Comparative 0. 4 2 2 1 0. 6 4 4 1 1. 2 5 4. 5 3 Present 1. 0 invention 2. 0 5 4. 5 4 2. 4 5 4. 5 4 Comparative 3. 0 5 4. 5 4. The numerals of the smoothness test results are the averages.
WO 89/09844 PCT/JP89/00291 JF6 Example Hot-dip zinc-aluminum alloy coated steel sheets were prepared by varying the bath temperature and the temperature of the steel sheet in order to confirm the effect of the temperature of the steel sheets to be dipped in the hot dipping bath according to the present invention (Example Each of the sheets was used as the material sheet. It was treated with a chromate. An epoxy resin paint containing 15% of a rustproof paint was applied thereto. After baking at 210°C for 35 sec, an under-paint having a dry thickness of 3 p was given. Then an oil-free polyester resin paint as the top-painting paint was applied thereto and baked at 220 0 C for 45 sec to form a top-paint having a dry thickness of 11 i.
The workability, adhesion and corrosion resistance of the prepainted steel sheets were determined.
The conditions and the results are shown in Table 21.
The workability was determined by the 2T bending test in the same manner as that of Example 1 and the results were evaluated on the basis of the standard shown in Table i.
The adhesion in the 2T part of the prepainted steel sheet was determined also in the same manner as that of Example 11 and the results were evaluated on the basis of the standard shown in Table 3.
The corrosion resistance test was conducted according to JIS Z 2371 in the same manner as that of Example 4. The flat part and 2T part were subjected 1 :1 WO 89/ is
I
*I
09844 PCT/JP89/00291 to the salt spray test (SST, 1000 The results were evaluated on the basis of the standard shown in Table 6.
It is apparent from Table 21 that when the temperature of the steel sheet to be dipped in the hot dipping bath is lower than the temperature of the bath, well-balanced, quite excellent workability, adhesion and corrosion resistance were obtained.
j Table 21 stee) Corrosion Bath composition J aheet resistance Bath temp. Work- Adhe- SST 1000 Hr temp. at dip- ability sion Al Si Pb Zn tC ingme1' fa 2T part part 0 40 420 5 5 5 0.1 460 420 5 5 5 0 480 400 5 5 5 0 480 440 5 5 5 5 Present' 2.0 0 460 440 5 5 5 invention 20 0 0. 005 balance 4040 0. 460 420 5 5 5 0.2 0 480 480 3 5 5 3 Cmaaie 0.5 0 400 465 5 5 5 0 480 485 5 5 5 5.0 0 460 470 5 5 5 The numerals o f the evaluation results are the ave~rages of the results.
~N
I
WO, 89/09844 PCT/JP89/00291 Example 16 Hot-dip zinc-aluminum alloy coated steel sheets 06 Exc'fneie were prepared by the process tated in Claim in which the temperatures of the bath and the sheet to be dipped in the bath, and the slit clearance, gas ejecting pressure and the distance between front and back nozzles of the gas wiping type of deposit control equipment were varied.
The sheets were treated with a chromate and then painted and baked by the two-coat/two-bake process in the same manner as that of Example 11 to form prepainted steel sheets. The surface smoothness of each of the prepainted steel sheets was determined on the basis of the standard shown in Table 11 in the same manner as that of Example 6.
The conditions and the results are shown in Table 22.
The bath composition was as follows: Al concentration 0.5 wt.% Pb concentration 0.005 wt.% Si concentration 0.01 wt.% Zn concentration the balance It is apparent from Table 22 that the surface smoothness of the prepainted steel sheets could be remarkably improved according to the present invention.
WO 8909844PC/JP89/00291 WO 89/09844 Table 22 (Bath D s a c m o h temp.) -Gas Dsac moh (Steel Slit eject- between ness sheet clear- ing front after temp. at ance pres- and back paint-' dipping (mm) sure nozzles ing timeW(C) I(kg/cm 2 (mm) Comparative -2 0 0.4 1.0 2 0 2 -2 0 0.6 1.5 2 03 -2 0 12 2.0 4 0 4 2.0 1.5 10 4. invention -6 0 2.4 0 .1 305 -8 0 1.2 0 .1 2 0 -8 0 2.4 2 .0 10 comparative -6 0 0 .8 1 .0 50 1 The numerals of the smoothness test results are the averages of the results.
r i I wo ps pg 8s 89/09844 PCT/JP89/00291
GRI
Example 17 Hot-dip zinc-aluminum alloy coated steel sheets O-F Ex ovipIle were prepared by the process -tated in Claim 7 in which the reheating temperature was varied. The sheets were treated with a chromate and then painted and baked by the two-coat/two-bake process in the same manner as that of Example 11 to form prepainted steel sheets. The surface smoothness of the prepainted steel sheets was determined on the basis of the standard shown in Table 11 in the same manner as that of Example 6.
The smoothness test results and the reheating temperatures are shown in Table 23.
The bath composition was as follows: Al concentration 0.5 wt.% Pb concentration 0.005 wt.% Si concentration 0.01 wt.% Zn concentration the balance The prepainted steel sheets having excellent smoothness could be thus prepared by the present invention.
WO 89/09844 PCT/JP89/00291 Table 23 Reheating temp. Smoothness after painting not.reheated 3 Comparative 380 3 400 3 420 4 Present 460 Present invention 500 560 The numerals of the smoothness test results are the averages of the results.
Example 18 The hot-dip zinc-aluminum alloy coated steel sheets prepared at various cooling speeds by the process 04: E C'M p I e- 9 stated in Claim 8were used. Each of the sheets was treated with a chromate and then painted and baked by the two-coat/two-bake process in the same manner as that of Example 11 to form prepainted steel sheets. The workability, adhesion and corrosion resistance of the prepainted steel sheets were determined. The results are shown in Table 24 together with the cooling speeds.
The workability was determined by the 2T bending test in the same manner as that of Example 1 and the results were evaluated on the basis of the standard shown in Table 1.
The adhesion in the 2T part of the prepainted II r WO 89/09844 PCT/JP89/00291 7( steel sheet was determined also in the same manner as that of Example 11 and the results were evaluated on the basis of the standard shown in Table 3.
The corrosion resistance test was conducted according to JIS Z 2371 in the same manner as that of Example 4. The flat part and 2T part were subjected to the salt spray test (SST, 1000 The results were evaluated on the basis of the standard shown in Table 6.
The bath composition was as follows: Al concentration 1.0 wt.% Pb concentration 0.005 wt.% Si concentration 0.01 wt.% Zn concentration the balance The prepainted steel plates having excellent workability, adhesion and corrosion resistance could be prepared by the present invention.
Table 24 Corrosion Cooling resistance Coolg Workability Adhesion resi speed 2T 2T SST 1000 Hr (°C/sec) flat part 2T part Comparative 5 5 5 5 5 5 5 20 5 5 Present invention 30 5 5 5 5 5 5 5 5 5 The numerals of the of the results.
evaluation results are the averages 2 WO 89/09844 PCT/JP89/00291' 7- Ii. .L J4LJ4Ut L %J 4- -1 R _R- Example Prepainted steel sheets of the present invention were prepared and the properties of them were determined as follows to confirm the effect of the present invention.
Hot-dip zinc-aluminum alloy coated steel sheets were prepared in a hot dipping bath having the following composition (Example 1) and they were used as the materials: The bath composition: Al concentration Pb concentration Si concentration 1.0 wt.% 0.005 wt.% 0.01 wt.% Zn concentration the balance Then the sheets were subjected to chemical conversion treatment to form a coating film in various amounts on the materials (hot-dip zinc-aluminum alloy coated steel sheets) with a chromate solution (type A) having a Cr to Si ratio of 55:45 which comprised a mixture of a solution containing silica having an average particle diameter of 10 mi (specific surface area: 200 m 2 and a solution containing silica having an average particle diameter of 50 my (specific surface area: 50 m in a ratio of 1:1; a chromate solution (type B) having a Cr to Si ratio of 55:45 comprising only the solution containing silica having an average particle diameter of 50 my (specific surface areai 200 m or a phosphate N;Pc e
C)
'am -Tr I r WO 89/09844 PCT/JP89/00291 r 13 solution.
Then an epoxy resin paint containing 15% of a rustproof pigment was applied to each of the treated zinc-aluminum alloy coated steel sheet. After baking at 210 0 C for 35 sec, an under-paint having a dry thickness of 3 p was given. Then an oil-free polyester resin paint as the top-painting paint was applied thereto and baked at 220 0 C for 45 sec to form a top-paint having a dry thickness of 11 i.
The scratch resistance, workability, adhesion and corrosion resistance of the prepared prepainted steel sheets were determined. The results are shown in Table 27 together with the conditions.
The scratch resistance was determined by applying a copper coin to the painted surface at an angle of 450 and moved under a load of 3 kg. The results were evaluated on the basis of the standard shown in Table 26.
The workability was determined by the 2T bend test in the same manner as that of Example 1 and the results were evaluated on the basis of the standard shown in Table 1.
The adhesion in the 2T part of the prepainted steel sheet was determined also in the same manner as that of Example 11 and the results were evaluated on the basis of the standard shown in Table 3.
The corrosion resistance test was conducted according to JIS Z 2371 in the same manner as that of Example 4. The flat part and 2T part of the prepainted t 1 ii WO 89/09844 PCT/JP89/00291 steel sheet were subjected to the salt spray test (SST, 1000 The results were evaluated on the basis of the standard shown in Table 6.
The prepainted steel sheets having not only excellent workability, adhesion and corrosion resistance but also an excellent scratch resistance could be prepared by the present invention.
Table 26 (Standard of evaluation of scratch resistance) Standard The area of the exposed under-paint was less than 10% and no sheet was exposed.
4 The area of the exposed under-paint was 10 to and no starting sheet was exposed.
3 The area of the exposed under-paint was more than 70% and that of the starting sheet was less than 2 The area of the exposed under-paint was 30 to 1 The area of the exposed under-paint was more than :3 fl)~u Bty i i I-i' I
I.
WO 89/09844 PCT/JP89/00291
X
Table 27 I Corrosion resistance Pretreatment Amount SST 1000 Hr (chemical of Scratch Work- Adheconversion coating resist-ability sion treatment film ance 2T 2T solution) (mg/m 2 flat part 2T part part 2 5 5 5 100 3 5 5 5 Chromate Comparative (type A) 150 3 5 5 5 200 3 5 5 5 300 2 5 5 5 3 5 5 5 Present 100 4 5- 5 5 invention- Chromate 150 4.5 5 5 5 1 5 0 4.5 5 5 5 (type B) 200 4.5 5 5 5 300 2 5 4 5 Comparative Phosphate 1000 5 4 3.5 4 4 The chromate solution of type A had a Cr to Si ratio of 55:45 and comprised a mixture of a solution containing silica having an average particle diameter of 10 my (specific surface area: 200 m and that having an average particle diameter of 50 mp (specific surface area: 50 m in a ratio of 1:1.
The chromate solution of type B had a Cr to Si ratio of 55:45 and comprised only a solution containing silica having an average particle diameter of mp (specific surface area: 200 m The numerals of the evaluation results in the above Table are the averages of the results.

Claims (8)

1. A process for the preparation of a hot-dip zinc-aluminum alloy coated steel sheet suitable for a prepainted steel sheet, comprising coating a steel sheet in a hot dipping bath compr'ising 0.3 to 3.5 wt.% of Al, 100ppm or less of Pb and the balance of Zn and incidental impurities, wherein the temperature of the steel sheet dipped in the hot dipping bath is lower than that of the hot dipping bath, and taking the steel sheet out of the hot dipping bath, wherein the amount of the molten zinc-aluminum alloy deposited on the steel sheet is controll.d with a gas wiping type of equipment for controlling the amount of molten zinc-aluminum alloy deposit under conditions comprising a slit clearance of 0.6 t 2.4 mm, a distance between front and back nozzles of *to 40 mm and an ejecting pressure of gas of 0.1 to kg/cm 2 S 2. A process according to Claim 1 wherein the hot S: dipping bath contains 1/100 to 1 part, per part of Al, of Si.
3. A process according to Claim 1 or 2 wherein the hot dipping bath contains 0.01 to 15 wt.% of Mg, Mn or Cu. A process according to any one of claims 1 to 3 i i '"yr 77 wherein the hot-dip zinc-aluminum alloy coated steel sheet is reheated to a temperature above the melting temperature of the coating layer. A process according to any one of Claims 1 to 4, wherein the hot-dip zinc-aluminum alloy coated steel sheet is cooled to the solidifying point thereof at a rate of at least
6. A process for the preparation of a prepainted steel sheet having an excellent workability and corrosion resistance comprising foLming a layer by chemical conversion treatment and further a surface painting film "layer on the hot-dip zinc-aluminum alloy coated steel sheet as prepared in any one of Claims 1 to
7. A process according to Claim 6, wherein the chemical conversion layer is formed by treating the sheet with a chromic acid solution containing silica having an average particle diameter of 50 um and a specific surface area of 200 m 2 /g in such a manner that the amount of the coating film after drying will be 50 to 250 mg/m 2 to impart an excellent scratch resistance.
8. A hot-dip zinc-aluminum alloy coated steel sheet as prepared in any one of Claims 1 to 5 and/or a prepainted steel sheet as prepared in Claim 6 or 7. 78
9. A process for the preparation of a hot-dip zinc-aluminum alloy coated steel sheet suitable for a prepainted steel sheet, comprising coating a steel sheet in a hot dipping bath comprising 0.3 to 3.5 wt.% of Al, 100ppm or less of Pb and the balance of Zn and incidental impurities, wherein the temperature of the steel sheet dipped in the hot dipping bath is lower than that of the hot dipping bath, reheating the hot-dip zinc-aluminum alloy coated steel sheet to a temperature above the melting temperature of the coating layer and cooling the hot-dip zinc-aluminum alloy coated steel sheet to the solidifying point thereof at a rate of at least 10 0 C/sec.
10. A process as claimed in Claim 9 wherein the hot e dipping bath contains 1/100 to 1 part, per part of Al, of Si. 0
11. A process as claimed in Claim 9 or 10 wherein the hot dipping bath contains 0.01 to 1.5 wt.% of Mg, Mn or Cu. *DATED THIS 11TH DAY OF MAY 1992 TAIYO STEEL CO., LTD. By Their Patent Attorneys GRIFFITH HACK CO. Fellows Institute of Patent Attorneys of Australia. ,L y
AU32886/89A 1988-04-12 1989-03-17 Hot-dip zinc-aluminum alloy coated steel sheet for prepainted steel sheet, process for producing the same and prepainted steel sheet Ceased AU628042B2 (en)

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JP63089998A JP2755387B2 (en) 1988-04-12 1988-04-12 Manufacturing method of hot-dip zinc-alloy-plated steel sheet for pre-coated steel sheet and pre-coated steel sheet
JP63-89998 1988-04-12

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AU3288689A (en) 1989-11-03
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ES2018368A6 (en) 1991-04-01
DE68923674T2 (en) 1996-04-04
FI895869A0 (en) 1989-12-08
DE68923674D1 (en) 1995-09-07
WO1989009844A1 (en) 1989-10-19
JPH01263252A (en) 1989-10-19
JP2755387B2 (en) 1998-05-20
EP0365682A1 (en) 1990-05-02
EP0365682B1 (en) 1995-08-02

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