AU595701B2 - An improved method and coating - Google Patents

Description

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P 146785 JGS:GS 2067T/15 595701

AUSTRALIA

PATENTS ACT 1952 COMPLETE SPECIFICATION

(ORIGINAL)

FOR OFFICE USE Application Number: Lodged: Complete Specification Lodged: Accepted: S* Published: 100.1-100 sl 6 U01R-! ;LL 11C.00 JU3W-,- :)Cp sTT Priority: .Related Art: RltdAt TO BE COMPLETED BY APPLICANT Name of Applicant: 9* .Address of Applicant: Actual Inventor: ,,Address for Service: Complete Specification METHOD AND COATING.

NIPPON MINING CO., LTD. and NIKKO AEN KABUSHISKI KAISHA 12-32, Akasaka 1-chome, Minato-ku, Tokyo, Japan and 8 Tenjinshin, Kurobe-shi, Toyama-ken, Japan Masatoshi Tomita Susumu Yamamoto Chikara Tominaga ARTHUR S. CAVE CO.

Patent Trade Mark Attorneys Level Barrack Street SYDNEY N.S.W. 2000

AUSTRALIA

for the invention entitled AN IMPROVED The following st-tement is a full description of this invention including the best method of performing it known to me:- 1 ASC 49 PATENT AND TRADE MARK ATTORNEYS

SYDNEY

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Field of the invention This invention relates to a colored zinc coating technique applied onto the surface of an iron or steel material, and particularly to a colored zinc coating method with the use of Ti-Zn or Ti-Mn-Zn system alloys by which the development of new colors not obtained by conventional techniques and clearer color developments compared to conventional ones are permitted. According to this invention, the developments of gold and dark red colors which could not have yet obtained are permitted and simultaneously yellow color, green color, blue color, purple color etc. may be more clearly developed. Thus, this invention provides colored zinc coated materials which are applicable to wider variety of fields and have coloring more suitable to the environment where they are placed.

Background of the invention Hot-dip galvanized iron and steel materials, coated by dipping in molten zinc, are used for corrosion protection purposes in a wide range of application, forming parts and facilities in the fields of building and construction, civil ergineering, agriculture, fisheries, chemical plants, electric power supply and communications, and so forth.

For pylons and other towers, lighting poles, guardrails, temporary stands and frames for various operations laiI 0 go 0 0 a

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1 and displays, shells and planks, and the like, there has been growing demand in recent years for colored hot-dip galvanized materials that present attractive appearances matching the environments involved, in preference to the classic hot-dip galvanized steels with metallic lusters.

With the spread of the aethetic sense the colored hot-dip galvanized articles show promise, with extensive potential demand in architecture, civil engineering, industrial plants, electric power supply and communications, transportations, agriculture, marine products and other industries.

Coloration of hot-dip galvanized steels has usually been by the application of paints. The method has the disadvantage of the paint film eventually coming off the coated surface. This results from the activity of Zn in the coating of the hot-dip galvanized steel that causes gradual alkali decomposition of the fatty acid constituting the oily matter in the paint, leading to the formation of zinc soap that hampers the adhesion of the paint film to the underlying surface.

In an effort to eliminate the disadvantage, a complex procedure has had to be followed. A steel article is first galvanized by dipping in a molten zinc bath. The coated steel is exposed to the air for one to three weeks so that corrosion products such as Zn(OH), ZnO, ZnCO 3 ZnCl 2 and the like deposit on the coated steel surface. The surface is then cleaned and colored.

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*055 0 0 *0*S Aside from the coating method described above, another approach that depends on the color-developing action of the oxide film in the hot-dip galvanizing is known in the art. For example, Australian Patent Application No. 24292/67 discloses a coloring treatment that uses a coating bath prepared by adding at least one element selected from titanium, manganese, vanadium and the like to a hot-dip galvanizing bath. However, the hot-dip galvanized coatings obtained by the disclosed technique use only up to 0.15 wt Ti and have been found to be generally very thin and light, with tendencies of rapid color fading and film separation with time. The desired color development is difficult to control precisely, often bringing out dim, indefinite hues.

For such reasons, even though many years have lapsed since its development, hot-dip galvanized coloring technique has not been put into practical use.

Under such circumstance, we succeeded in developing an excellent colored zinc coating technique and accomplished a remarkable advance in the art by using a galvanizing zinc alloy containing 0.2-0.7 wt Ti which may or may not further comprise one or more of the following: 1.0-5.9 wt Pb, 0.05-0.2 wt Cd, 0.05-0.15 wt Mn, 0.01-0.05 wt Cu 0.01-0.05 wt Sn, 0.01-0.05 wt Bi, 0.01-0.05 wt Sb, or d VA 0185o 3

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i IC.i~*~II i 0.01-0.05 wt In in said alloy, hot-dipping a base metal of iron or steel into the bath of said alloy, at a bath temperature of 450-620°C, and allowing the plated material produced to cool in air or heating the plated material to 450-620 0 C followed by the cooling, and thereafter cooled with cold or warm water or with a coolant gas. According to the above proposed method, it was possible to form on said base metal a clear, uniform, brightly coloured coating selected from; yellow, purple or blue color using 0.5 Ti-Zn alloy, for example, by controlling its oxidization conditions. Further it became possible to develop a dark-blue, blue or light green colored coating, using 0.5 Ti 0.1 Mn-Zn alloy by controlling its oxidization conditions, wherein said colored coating adheres well to said base metal.

4 Therefore the present invention discloses a zinc alloy 0 with the above compositions together with a method of forming said zinc alloy.

However, there is still a steady demand in the art for many improvements such as: the development of new colorings which have not yet been obtained in past, (b the obtainance of the color developments which are more beautiful and clearer than ones previously obtained, the enhanced stability of color development, that the inherent corrosion resistance of galvanized zinc coating is not sacrificed, Z< SR4/4 less change with the lapse of time, and l to provide easy and stable operation.

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Obect of the invention The object of this invention is to establish colored zinc coating technique by which the above mentioned improvements may be attained using Ti-Zn or Ti-Mn-Zn zinc alloys.

Summaryof the invention Toward the above object, we have made many efforts. In the colored hot-dip galvanizing, the composition of the plating bath and the conditions of producing an oxidized

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a'oe -iv T O 4a 0185o .i i; i- 1 1 r film delicately combine to present coloring effects by light interference. By ingeniously controlling these factors, in Ti-Zn alloys, we successfully attained the development of golden color which had been thought that such trial is beyond the range of possibilities, and suceeded in developing dark-red color which has strongly desired. In addition, it became possible to stably attain the development of clearer yellow, purple, green -r other roln...compared to ones previously obtained. Further, in Ti-Mn-Zn alloys, we were successful in developing a strongly needed dark-red color, and in stably obtaining yellow, green and blue color clearer than previous ones.

This invention also found that colored zing coating may be applied by spraying method.

The change of the colored zinc coating with the lapse e* 00 of time may be suppressed by painting thereon.

Detailed explanation of the invention Zinc alloy hot dipping is carried out by melting a zinc alloy in a coating bath and immersing a member to be coated 0 thereinto.

A-l) The development of golden color with Ti-Zn alloy It is possible to form a colored coating with a golden hue on an iron or steel surface by plating the base metal using a bath of a zinc alloy for hot dipping of a composition comprising 0.1 0.5 wt Ti bal. Zn at a bath temperature of 450 470°C, allowing the plated work to stand in air for 5 20 seconds, and thereafter cooling it with cold or warm water.

The metallic zinc bullion to be used in forming the zinc alloy for hot dipping is typically one of the grades conforming to JIS H2107,' for example, distilled zinc ist grade (at least 98.5 pure), purest zinc (at least 99.99 pure), and special zinc grades. The impurities inevitably contained in these zinc materials are,.for example, in the distilled zinc 1st grade, ip to 1.2 wt Pb, 0.1 wt Cd, and 0.020 wt Fe. For the purposes of the invention a metallic zinc with a total impurity content of less than wt is desirable. Particularly, distilled zinc is 0@*OS@ preferred because it permits to effect plating with the use of ordinary flux and color strength produced becomes higher.

e* In the embodiment, the plating is carried out using a molten zinc alloy bath of the composition 0.1 0.5 wt Ti bal. Zn, obtained by adding 0.1 0.5 wt Ti to the above-mentioned zinc. A bath of a molten zinc alloy containing 0.3 wt Ti is particularly desirable.

In order to produce the golden colored coating from the hot-dip zinc alloy bath of the above composition, a base metal of iron or steel is immersed in the plating bath at 450 470 0 C for at least one minute, the base metal is pulled out of the bath and allowed to cool in air for about 20 seconds, and then is immediately cooled with cold or warm water to form thereon an oxide film with a golden hue.

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Thus, in producing a golden colored coating, it is essential to immerse the iron or steel base metal in the bath of molten zinc alloy of the composition 0.1 0,5 wt Ti bal. Zn at a bath temperature of 450 470 0 C and then allow it to cool in air for a very short period of about 5 seconds, preferably for 10 20 seconds. If the conditions are outside the ranges specified above, the desired golden hue will not result. For example, if the heating temperature is above 470 0 C and the period of time for which the plated works in allowed to cool in air exceeds seconds, the hue of the coating will turn purplish.

As stated hereinbefore, a colored coating with a uniform, stable golden hue can be formed on a base metal of iron or steel by plating it under specific conditions using a molten zinc alloy of the specific composition. It thus provides a corrosion-resistant material for the components and facilities for uses where they are required to be golden in color from the aethetic viewpoint. The iron or steel products with colored coatings of the invention are highly corrosion-resistant and are of value in a wide range of use.

A-2) The development of clear purple color with Ti-Zn alloy It is possible to form a colored coating with a purple hue on an iron or steel surface by plating the base metal using a bath of a zinc alloy for hot diiping of a composition comprising 0.1 0.5 wt Ti bal. Zn at a bath temperature of 500 550 0 C, either allowing the plated work 7 p .0 to cool in air for 10 50 seconds or heating it in an atmosphere at 500 520°C for 10 20 seconds, and thereafter coolig it with cold or warm water. With regard to a zincli±3=e±±B, the same explanation as in A-l) is applied hereto.

The plating is carried out using a molten zinc alloy bath of the composition 0.1 0.5 wt Ti bal. Zn, obtained by adding 0.1 0.5 wt preferably 0.3 wt Ti to the above-mentioned zinc.

:0 In order to produce the purple colored coating from the hot-dip zinc alloy bath of the above composition, a base metal of iron or steel is immersed in the plating bath at 500 5500°C, preferably at 500 5200°C, for at least one minute, the base metal is pulled out of the bath and allowed to cool in air for about 10 50 seconds, preferably for 50 seconds, and then is immediately cooled with cold or warm water to form thereon an oxide film with a purple hue.

Alternatively, the work taken out of the bath is heated in an atmosphere at 500 520°C for 10 20 seconds and then is cooled with cold or warm water to form a purple colored oxide film thereon.

95 Thus, in producing a purple colored coating, it is essential to immerse the iron or steel base metal in the bath of molten zinc alloy of the composition 0.1 0.5 wt Ti- Bal. Zn at a bath temperature of 500 5500°C, preferably of 500 5200°C, and then either allow it to cool in air for a very short period off 10 50 seconds, preferably of 40 -8- I seconds or heat it in an atmosphere at 500 520 0 C for 20 seconds and then cool it with cold or warm water. If the conditions are outside the ranges specified above, the desired purple hue will not result.

As stated hereinbefore, a colored coating with a uniform, stable purple hue can be formed on a base metal of iron or steel by plating it under specific conditions using a molten zinc alloy of the specific compostion. It thus provides a corrosion-resistant material for the components c and facilities for uses where they are required to be purple in color from the aethetic viewpoint.

The iron or steel products with colored coatings of the invention are highly corrosion-resistant and are of value in a wide range of use.

A-3) Selective development of yellow-dark red-green vaE 0 A with Ti-Zn alloy There is provided a zinc alloy for colored hot-dip galvanizing capable of developing yellow, dark red, aFF green colors selectively as desired, composed of 0.2 0.7 wt Ti and the balance zinc and inevitable impurities.

*0 It has further been found that the following alloys, made by adding the ingredients as follows to the above Ti-Zn alloy, are useful in uniform coloring in yellow, dark red, and green: A zinc alloy for colored ho-dip galvanizing capable of developing yellow, dark red, an greenicolors 1_7 ^riA ;r selectively as desired, composed of 0.2 0.7 wt Ti, 1.3 5.9 wt Pb, and the balance zinc and inevitable impurities.

A zinc alloy for colored hot-dip galvanizing capable of developing yellow, dark red, aal green colors selectively as desired, composed of 0.2 0.7 wt Ti, 1.2 1.3 wt Pb, 0.1 0.2 wt Cd, and the balance zinc and inevitable impurities.

A zinc alloy for colored hot-dip galvanizing capable of developing yellow, dark red, a d green)colors and desired, composed of 0.2 0.7 wt Ti, 1.0 1.2 wt Pb, 0.05 0.2 wt Cd, 0.01 0.05 wt of at least one element S selected from the group consisting of Cu, Sn, Bi, Sb, and In, and the balance zinc and inevitable impurities.

*A base material of iron or steel is galvanized by immersion in a molten zinc bath of such an alloy, and the coated metal is allowed to cool in the air or is heated at a *specidic temperature. Through proper control of the conditions, it is possible to bring out yellow, dark red, and green colors selectively at will. Even with an alloy based on a purest metallic zinc (at least 99.995% pure) or special zinc (at least 99.99 pure), galvanizing with good wettability and uniformity in hue i .'r.lved, Zinc alloy hot di;r ,w -lried out by melting a zinc alloy in a coating b" i.rmersing a work to be galvanized in the bath. The zinc alloy is prepared by adding a specific alloying additive to a metallic zinc. In the practice of the invention, a metallinc zinc bullion with

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R,44/ 10 a high purity of at least 99.9 typified by a purest zinc (99.995 pure) and special zinc (at leat 99.99 pure) as defined in JIS H2107, in used. This prevents any adverse effects the variable introduction of impurities (Pb, Cd, Fe, etc.) can have upon the controllability of color development. Nevertheless, the use of such a high purity zinc brings shortcomings while it eliminates variations in the coating conditions due to the presence of impurities. For example, when an iron or steel material is galvanized by immersion in a coating bath (Fe saturated) containing .predetermined amounts of Ti and Mn, the formation of an Soxide film on the bath surface is rapid and large in amount.

So." These and other factors tend to produce color shading, such 0@000

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as partial two-color mixing of the colored oxide film of the coating layer.

Under the circumstances the present inventors have 0 0 found that the addition of 0.2 0.7 wt Ti is effective in

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giving a yellow, dark red, or green color clearly and brightly without partial lackness of plating or unevenness in color.

o If the Ti content in the coating bath is less than 0.2 o wt the formation of a colored oxide film in the coating layer of the galvanized metal is inadequate, and the hue is low and ununiform, thus reducing the marketable value of the colored galvanized product. If the Ti content is above 0.7 wt the oxide film forms too rapid and the change in hue oo the colored oxide film becomes too fast to control.

11 I A Moreover, too much oxide formation on the coating bath reduces the wettability of the bath with respect to the base metal to be galvanized.

For the further improvement in the coating wettability, variou alloys, prepared by adding Pb, Cd, Sn, Bi, Sb, In, and/or the like to the 0.2-0.7 wt Ti bal. Zn alloy, were investigated. As a result, the zinc alloys and referred to above have now been found particularly useful.

These three alloys will be described below.

Alloy containing 1.3-5.9 wt Pb in addition to Ti:- If the Pb content is less than 1.3 the wettabilityimproving effect is limited. In colored coating at a bath temperature of 470-500°C partial uncoating will result.

Especially in the bath temperature range of 470-490°C dross deposition on the coating film will frequently occur. In the fee 500-600 0 C range unplanted portions where coating to be plated does not adhere onto the surface of a material to be plated leaving the surface of the material partially uncaoted and color shading in the colored oxide film will result. The Pb see* addition proves increasingly effective up to the limit of its solubility. Since the Pb solubility in molten zinc at a bath temperature of 600 0 C is 5.9 wt the value is taken as the upper limit.

Alloy containing 1.2-1.3 wt Pb and 0.1-0.2 wt Cd in addition to Ti:- Where Pb and Cd are combinedly used, small additions can prove effective. If the Pb content is less than 1.2 wt 12 0147o ~xri*mjuY-~pl~.vi, partial uncoating occurs in the coloured coating at a bath temperature of 470-600'C, even in the present of Cd. In 0 V a I 0* *12a 0147o the temperature range of 470 490 0 C the possibility of dross deposition on the coating film will be greater. Even when the Pb content is within the specified range, similar troubles will take place if the Cd content is less than 0.1 wt If the Pb content exceeds 1.3 wt or the Cd content is more than 0.2 wt the oxide formation on the coating bath becomes so much that the rate of uncoating rises.

c) Alloy containing, besides Ti, 1.0 1.2 wt Pb, 0.05 0.2 wt Cd, and 0.01 0.05 wt of at least one or more element selected from Cu, Sn, Bi, Sb, and In:se* The addition of at least one element selected from Cu, Sn, Bi, Sb, and In promotes the wettability-improving effect of Pb and Cd. If the Pb content is less than 1.0 wt and the Cd content below 0.05 wt partial uncoating results from colored galvanizing at a bath temperature of 470 600 C. Especially in the bath temperature range of 470 S' 490 0 C the dross deposit on the coating film will increase.

On the other hand, if the Pb content is more than 1.2 wt and the Cd exceeds 0.2 wt much oxide formation on the coating bath surface is observed. The addition of 0.01 0.05 wt of at least one of Cu, Sn, Bi Sb, and In retards the rate of oxide film formation on the bath surface and i improves the wettability for the work to be galvanized.

The addition elements thus prevent uncoating, color shading, dross deposition, and other troubles, render it easy to control the hue of the colored oxide film, and 13

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In the hot dip galvanizing with such a zinc alloy, the work to be galvanized is degreased, for example by the use of an alkaline bath, descaled by pickling or the like, and then treated with a flux to be ready for galvanizing. The flux treatment is effected, for example, by a dip for a short time in a ZnCl 2 -KF solution, ZnCl 2

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4 Cl solution, or other known flux solution.

After the pretreatment, the works is immersed in a oS Soo-t 6 i o 0 ccoating bath at a ap 1eific contr-e!e temperature for 1 to 3 minutes. The coated metal is pulled out of the bath and, through proper control of the degree of oxidation, a yellow, dark red, or green color is selectively obtained at will.

For instance, after the coated work has been pulled out of the bath, it is cooled under control by natural cooling in the air, cooling with cold or warm water, slow cooling in an oven, or by other means.

Alternatively, the coated metal from the bath is held in an atmosphere at 450 550 0 C for a predetermined period of time, so that the degree of its oxidation can be controlled. The holding temperature, holding time, and subsequent cooling method are chosen as desired.

As the degree of oxidation is increased, yellow, dark red, and green colors are developed successively in the order of mention.

An example of the oxidation degree control is as follows: 14 -d _i iA' jC o ~:C ~o$ i Yellow: After the work has been pulled out of the coating bath at a bath temperature of 590 0

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it is held in an atmosphere at 500 0 C for 15 seconds and then is cooled with warm water.

Dark red: The bath temperature is increased by 0 C, and either is atmosphere temperature is raised or the holding time is prolonged by seconds.

a a a *a 0 a a O e Green: The bath temperature is made even higher by 10 0 C, and either the atmosphere temperature is further increased or the holding time is extended by a further period of 5 second.

With the alloys of the invention, the Ti 1.3 5.9 wt Pb bal. Zn alloy, Ti 1.2 1.3- wt Pb 0.1 0.2 wt Cd bal. Zn alloy, and Ti 1.0 1.2 wt Pb 0.05 0.2 wt Cd 0.01 0.05 wt (Cu, Sn, Bi, Sb, and/or In) bal. Zn alloy, the color development is controllable in the order of golden, purple, and blue hues.

In the order of increasing degrees of oxidation, gold, purple, blue, yellow, dark red, and green colors are brought out.

B-l) The development of dark-red color with Ti-Mn-Zn alloy It is possible to form a colored coating with a dark red hue on a base metal of iron or steel by plating the base 15 r coating is not sacrificed, less change with the lapse of time, and to provide easy and stable operation.

-4- 0185o I 0 0 50 00 0 0000.0 0 0 *860*0 00 0 metal using a bath of a molten zinc allay of a composition comprising 0.2 0.5 wt Ti 0.05 0.15 sat Mn bal. Zn at a bath temperature of 580 600 0 C, heating the plated work in an atmosphere at 500 520 0 C for 30 70 seconds, and thereafter cooling it with cold or warm water.

The metallic zinc to be used in forming the zinc alloy for hot dipping is typically one of the grades conforming to JIS 112107, for example, distilled zinc 1st grade (at least 98.5 pure), purest zinc (at least 99.99 pure), and special zinc grades. The impurities inevitably contained in these zinc materials are, for example in the distilled zinc 1st grade, Ja1iP1.2 wt Pb, 0.1 wt Cd, and 0.020 wt Fe. For the purposes of the invention a metallic zinc with a total impurity content of less 'than 1.5 wt is desirable.

Among these zinc varieties, distilled zinc is preferred practically because it can be plated with ordinary flux and the concentration is high.

Under this embodiment the plating is carried out using a bath of molten zinc alloy made by adding 0.2 0.5 wt preferably 0.3 wt Ti and 0.05 0.15 wt perferably 0.1 wt Mn to the above-mentioned zinc.

In order to produce the dark red colored coating from the hot-dip zinc alloy bath of the above composition, a base metal of iron or steel is immersed in the plating bath at 580 600 0 C for at least one minute, the base metal is pulled out of the bath and held in an atmosphere at 500 520 0 C (for example in an oven) for 30 70 seconds, and then 16 T 0 4a 0185o I e is immediately cooled with cold or warm water to form thereon an oxide film with a dark red hue.

Thus, in producing a colored coating with a specific dark red hue, it is important to plate the iron or steel base metal using the bath of the molten zinc alloy of the specific composition at the specific bath temperature, heat it under specific temperature conditions, and then cool it with cold or warm water. If the conditions are outside the ranges specified above, no coating with the desired dark red hue be obtained.

0:06 B-2) The development of green color with Ti-Mn-Zn alloy Using a zinc alloy for hot dipping to form on a base surface a green colored coating containing 0.2 0.5 wt Ti and 0.05 0.15 wt Mn, it is possible to produce a green colored coating on an iron or steel surface by coating the base metal with the zinc alloy for hot dipping at a bath temperature of 600 620 0 heating the coated work in an atmosphere at 500 520 0 C for 50 60 seconds, and thereafter cooling it with cold or warm water or with a coolant gas.

The zinc to be used is in accordance with B-l).

The coating is carried out using a molten zinc alloy bath of the above-mentioned zinc with the addition of 0.2 0.5 wt Ti and 0.05 0.15 wt Mn. The use of a hot-dip bath of a zinc alloy containing 0.3 wt Ti and 0.1 wt Mn is particularly desirable for forming a green coloted -17 coating.

In order to produce the green colored coating from the hot-dip bath of the zinc alloy containing the abovespecified percentages of Ti andi Mn, a base metal of iron or steel is immersed in the molten zinc alloy bath at 600 620 0 C for at least one minute, the base metal is then pulled out of the bath and heated in an atmosphere (for example, in an oven) at 500 520 0 C for 50 60 seconds. After the heating, the work is cooled with cold or warm water or with coolant gas to form thereon a colored coating of an oxide with a green hue.

As described above, a colored coating with a uniform, g* stable green hue can be obtained by conducting the plating by the use of a hot-dip bath of molten zinc alloy containing e~g..0.2 0.5 wt Ti and 0.05 0.15 wt Mn under the specifi- Ce. *ed condition. If the Ti and Mn contents in the zinc alloy are outside the ranges specified, the green hue of the S resulting colored coating will be uneven and the oxide film will show poor wettability with respect to the coated base metal.

Also if the bath temperature and subsequent heating temperature and time as hot-dip conditions are not within the specific ranges, other hues can mix in, rendering it impossible to give a coating with a uniform green hue.

Thus,. in producing a green colored coating uniform in hue, important roles are played by the Ti and Mn contents in the molten zinc alloy for the hot-dip bath, the hot-dip 18 6 conditions, and the subsequent heating conditions. It is only by the combination of such specific conditions that the objective green colored coating is obtained.

The colored coating formed excellently resists corrosive attacks with the so-called corrosion weight loss by far the less than that of coatings using ordinary molten zinc alloys.

B-3) The development of yellow color with Ti-Mn-Zn alloy S*"It is possible to form a colored coating with a yellow i hue on an iron or steel surface by plating the base metal with a zinc alloy for hot dipping containing 0.2 0.5 wt sees Ti and 0.05 0.15 wt Mn at a bath temperature of 580 600 0 C, heating the plated work in an atmosphere at 500 520 °C for 20 30 seconds, and thereafter cooling it with cold *or warm water or with coolant gas.

The zinc to be used is according to B-1).

S* 'The plating is carried out using a molten zinc alloy bath of the above-mentioned zinc with the addition of 0.2 0.5 wt Ti and 0.05 0.15 wt Mn. A bath of a molten

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zinc alloy containing 0.3 wt Ti and 0.1 wt Mn is particularly desirable.

In order to produce the yellow colored coating from the hot-dip bath of the zinc alloy containing the abovespecified amounts of Ti and Mn, a base metal of iron or steel is immersed in the plating bath at 580 600 0 C for at least one minute, the base metal is then pulled out of the 19 7 bath and heated in an atmosphere (for example, in an oven) at 500 520 0 C for 20 30 seconds. After the heating, the work is water-cooled for about 10 seconds to form thereon a colored coating of an oxide with a yellow hue.

Thus, in producing a yellow colored coating, it is especially important to perform the plating by the use of the bath of molten zinc alloy of the specific composition under the specific conditions and then heat the plated work in an atmosphere at 500 520 0 C for 20 30 seconds. If the o.

S"heating after the plating is done under conditions outside *eoee S" the ranges specified above, no uniform yellow hue will be oooo attained. For example, if the heating time exceeds o seconds the color hue will be mixed with green, and the 0 desired yellow colored coating will no longer be obtained.

The colored coating obtained is excellent in its corrosion resistance.

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B-4) The development of blue color with Ti-Mn-Zn alloy It is possible to form a colored coating with a blue hue on an iron or steel surface by plating the base metal using a bath of a zinc alloy for hot dipping of a composition comprising 0.1 0.5 wt Ti 0.05 0.15 wt Mn bal. Zn at a bath temperature of 530 550 0 C, allowing the plated work to cool in air for 15 25 seconds, and thereafter cooling it with cold or warm water.

The zinc to be used is in accordance with B-l).

The plating is carried out using a bath of molten zinc 20 8 i alloy made by adding 0.1 0.5 wt preferably 0.3 wt titanium (Ti) and 0.05 0.15 wt preferably 0.1 wt manganese (Mn) to the above-mentioned zinc.

In order to produce the blue colored coating from the hot-dip zinc alloy bath of the above composition, a base metal of iron or steel is immersed in the plating bath at 530 550 0 C, for at least one minute, the base metal is pulled out of the bath and allowed to cool in air for about *15 25 seconds, and then is immediately cooled with cold or p.

warm water to form threon an oxide film with a blue hue.

Thus, in producing a blue colored coating, it is essential to plate the iron or steel base metal using the bath of molten zinc alloy of the composition comprising 0.1 0.5 wt Ti 0.05 0.15 wt Mn bal. Zn at a bath temperature of 530 550 0 C, and then allow it to cool in air for a short period of 15 25 seconds. If the conditions 0@ are outside the ranges specified above, no coating with the desired blue hue will result.

The colored coating obtained in excellent is its corrosion resistance.

It was found to be effective to further include Ce in the alloys used in said A) and B).

C) After-treatment The colored oxide film formed on the colored, hot-dip galvanized material tends to discolor or fade with time, with changes in hue due to the progress of deterioration, 21-

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*s -I~__lr depending on the environmental conditions including the sunlight, temperaiure, and humidity. Although the deterioration of the colored oxide film, of course, does not adversely affect the corrosion resistance of the hot-dip galvanized steel itself, the original beautiful appearance is unavoidably marred.

As a simple measure for protecting the colored oxide film on the colored hot-dip galvanized material to suppress the discolor or fade with time, surprisingly, painting has been found appropriate for realizing the object. As noted already, painting of the coated surface of ordinary (uncolored) hot-dip galvanized steel poses the problems of inadequate adhesion or separation of the paint film on short-period exposure. Partly responsible for them is the deposits on the galvanized steel surface of oxides (zinc white rust) and flux such as ammonium chloride used for the galvanizing. Presumably responsible too is the basic zinc dissolution product formed between zinc and the water that has permeated through the paint film. It is presumed that this product acts to decompose the resinous content (oily fatty acid) of an oily paint or long oil alkyd resin paint, causing the decomposition product to react with the zinc to produce zinc soap along the interface between the zinc surface and the paint film, thereby substantially reducing the adhesion of the paint.

A common belief has been that the colored oxide film layer formed on the surface of the colored hot-dip <1 22 w i galvanized steel does not provide an adequate barrier between the zinc surface and the surrounding air. The pessimistic view that painting over the oxide film would, after all, be the same as direct paint application to the galvanized surface has been predominant. Contrary to these predictions, it has now been found that the colored oxide film has good affinity for and adhesion to paints, allowing the applied paint to permeate through the film to show high separation resistance, and is sufficiently capable of *9 *S 06 S° preventing water permeation to inhibit the reaction of the zinc layer with water and therefore the formation of zinc eowu• S, 0 soap.

690V In accordance with the invention, the hot-dip galvanized materials thus colored may be coated with a paint S ,having excellent adhesion, weather resistance, durability, and environmental barrier properties.

For the painting of ordinary hot-dip galvanized steels, pretreatment is essential and the types of paints that may be employed are limited. With colored, hot-dip galvanized 5.5.5.

S* steels, by contrast, there is no need of pretreatment and various paints may be used. Since the heating for oxidation that follows the galvanized step produces a film of oxide such as TiO 2 or MnO on the galvanized surface, the coating on the galvanized steel is so clean that there is no necessity of treating the surface before painting.

The paint to be used may be any type which does not unfavorably affect, but protect, the colored oxide film 23 i_

I

*r 0 0 a.

0

U

.9, a OS layer to be painted. Typically a synthetic resin paint is used. Among synthetic resin paints, those superior in protective effects are polyurethane resin, acrylic resin, epoxy resin, and chlorinated rubber paints. The paint is properly chosen in consideration of the price, environments to be encountered, ease of application, and other factors.

Where the color of the colored oxide film is to be showr. as it is, a clear paint is the best choice, and where the color tone is to be modified, an aqueous paint is the easiest to handle. In any case, the paint can be applied by brushing, spraying, or dipping.

In certain situations multicoating is not impractical.

For instance, where the environments are very severe or adverse, multiple painting may be taken into account. An example is the application of an aqueous paint as the base coat and a clear paint as the intermediate and top coats.

Alternatively, an epoxy resin paint durable against the alkali attacks that result from zinc elution may form the undercoat and a chlorinated rubber or polyurethane paint excellently resistant to water, chemicals, and weather may form the intermediate and surface coats.

Even if the paint degrades with time, leading to chipping or flaking of the coat, the beautiful appearance of the galvanized steel will remain unaffected thanks to the colored oxide film on the steel surface. Under the invention, such chipping or flaking seldom takes place because the paint pe):meated through and binds solidly with 2 nt a 24 ii the colored oxide film. The paint that had permeated the oxide film keeps off water and the like by its waterrepelling action and thereby protects the film.

D) Spraying For the colored hot-dip galvanizing it is prerequisite that the work to be coated be dipped in a molten zinc alloy bath. In the practice, therefore, there are sometimes met the following limitations: The process is difficult-to apply to shapes too :''"large to be dipped in the bath.

The coating of assembly parts and structures is ooeo sees sometimes difficult.

ooooo Localized coloring is cumbersome. Although masking and other techniques may be resorted to, they sinvolve much complexities and difficulties. The techniques are difficult to cope with the trend toward more frequent situations requiring pattern drawing for decorative purposes.

For repairs of installations and the like the *.*process is difficult to practice at sites.

There are tendencies that the larger the content of such an alloying element as Ti and Mn, the worse the wettability of the bath and the more the number of holidays 2W" and other coating defects. Although an increase in the content of the additive element improves the durability of the resulting coating accordingly, such addition is sometimes difficult from the standpoint of the coating technology.

25 l II Ill I.t I

S

0S*S

S

0@

S@

*5 S *5 S.

S

S

S

95 5 0 9 The process sometimes brings failure of coating and other coating defects.

The colored zinc coating by metal spraying basically involves spraying a zinc alloy, which is otherwise used for a coating bath, in the form of wire, rod, or powder, over the object. Surprisingly, the oxidation reaction of the additional element had been found to proceed more favorably than expected during the spraying process, achieving at least as satisfactory effects as the colored hot-dip galvanizing.

Thus, in the present invention, a colored zinc coating may be attained by spraying a coloring, oxidizing zinc alloy over a base surface by a metal spraying process, whereby a colored oxide film is formed on the base surface. After the spraying, the color development of the colored oxide film may be controlled by cooling and/or heating.

Metal spraying comprises heating a sprayable material to a half-molten state and spraying it over a base surface to form a coating tightly bonded to the surface. The sprayable material takes the form of a wire, rod, or powder, any of which may be employed under the invention.

The sprayable material may be any of the zinc alloys in common use for colored hot-dip galvanizing. It may, for example, be a Ti-Zn, or Ti-Mn-Zn alloy with or without the further addition of Cu, Ni and/or Cr. In the case of hot dipping, a work high in Ti, Mn or the like is not readily wetted when dipped in the bath, leaving holidays on the 26 13 U III J11 a a a.

a a. a surface. The possibility of uncoating puts limitations to the amounts of the additive ingredients. Metal spraying is free from the wettability problem, and larger proportions of the additional elements can be used. Accordingly, the range of uolor development is wider and the hues have longer life.

An example of desirable sprayable material is a zinc alloy containing 0.1 2,0 wt Ti and optionally 0.01 4.0 wt of at least one selected from Mn, Cu, Cr, and Ni. With good workability the zinc alloy can be easily made into a wire or rod or powdered by crushing or melt dropping.

The sprayer that may usually be used is of the type known as a gas flame spray gun. An arc type spray gun may be employed as well.

The sprayable material is melted by the sprayer and sprayed over the base surface to be coated. The corners and intricate portions of the work difficult to coat by hot dipping can be completely coated by aiming the spray gua- to those portions. Localized coatability permits figures and other patterns to be made easily. Another major advantage of metal spraying is the ability of coating iron and steel structures or the like at the sites.

After the spraying, the degree of surface oxidation is controlled so as to develop a desired color. A variety of colores, yellow, dark red, green, golden, purple, and blue colors, can be selectively developed as desired, depending on the degree of oxidation. For the oxidation control, the cooling rate of the sprayed coat can be 27 i 0 /CD -14adjusted by the use of natural cooling in the air or forced cooling with water or air. Also, the spray coat may be heated for a variable period with flame, infrared lamp, oven (where usable) or the like, and the subsequent cooling may be controlled. Proper combination of the sprayable material composition and su'face oxidation conditions renders it possible to bring out a desired hue.

In this way a zinc sprayed coating with both corrosion resistance and colorability is produced.

The painting described above may be applied onto the sprayed coating.

The functional effects of the spraying are summerized as follows: Applicable to large components that cannot be hot-dipped.

0* 2. Capable of easily coating the portions of assembly parts and structures difficlut to hot-dip.

3. Permits localized color development and display of a desired figure or other pattern thus enhancing the decorative value of the coating.

Possibility of coating at the site.

Ability to use high-melting alloys.

6. Ease of forming a thick coat suited for providing long-term corrosion protection.

7. A high Ti content in the alloy enhances the corrosion resistance and enriches the color hue.

8. The coating film, with a rough and porous surface, -28 15 is suited as a base to be painted, and painting with a clear paint or various colored dyes can improve the durability of the colored oxide film of the coating.

other than spraying process, vapor deposition process, sputtering process, ion plating process or other surface coating process may be applied in this invention.

The Examples will be described below: The Examples A to D correspond to the items A to D described in the detailed explanation.

Example A 1 (development of golden color with Ti-Zn alloy) see 09490:A test piece of steel sheet, SS4l, 50 mm wide, 100 mm long, and 3.2 mm thick, was degreased by immersion in an 0 00 alkaline bath at 80 0 C for 30 minutes. It was washed with warm water, and then derusted by immersion in a 10 hydrochloric acid bath at ordinary temperature for minutes.

Next, the steel sheet was washed with warm water and was fluxed by a dip in a solution containing 35 ZnCl 2

-NH

4 Cl at 60 0 C for 30 seconds.

The steel sheet thus pretreated was plated by immersion in a plating bath of the composition comprising 0.3 wt Ti -bal. Zn at 450 4700~C for one minute. It was pulled out of the bath, allowed to cool in air for 10 20 seconds, and was immediately cooled with water at ordinary temperature.

The steel surface so obtained had a coating of oxide with a 29 16 i;i-

LI

C

C. CC

C

C

C

*5 lustrous, uniform golden hue.

The test piece of steel sheet with color coating thus obtained was subjected to a salt spray corrosion test for 240 hours. The corrosion weight loss was 72 g/m 2 By way of comparison, ordinary plated steel sheets hot-dip galvanized with distilled zinc were likewise tested.

The corrosion weight loss amounted to as much as 120 150 2 g/m 2 Example A 2 (development of purple color with Ti-Zn alloy) The steel sheet pretreated in the same manner as the previous example was plated by immersion in a plating bath of the composition comprising 0.3 wt Ti bal. Zn at 500 520 C for one minute. It was pulled out of the bath, allowed to cool in air for 40 50 seconds, and was immediately cooled with water at ordinary temperature.

The steel surface so obtained had a coating of oxide with a uniform purple hue.

The test piece of steel sheet with color coating thus obtained was subjected to a salt spray corrosion test for 240 hours. The corrosion weight loss was 63 g/m 2 By way of comparison, ordinary plated steel sheets hot-dip galvanized with distilled zinc were likewise tested.

The corrosion weight loss amounted to as much as 120 150 g/m 2 g/m

OOSSCC

C C C. Ce

C

J

30 17 Example A 3 (development of yellow dark red green color and additional development of gold purple blue color) The individual pieces pretreated as described previously were immersed in coating baths of the compositions given in Table 1 for one minute and ihen were pulled out at a rate of about 6 meters per minute. The steel pieces thus taken out of the baths were heated in an atmosphere at 500 0

C

for given periods of time, and cooled with warm water to *form the following colored oxide films.

The treating conditions were as follows:

S

Yellow Bath temperature 590 0

C

4 Holding at 500 0 C for 15 20 seconds Dark red: Bath temperature 600 0

C

Holding at 500 0 C for 25 30 seconds Green Bath temperature 610 0

C

4- Holding at 500 0 C for 35 40 seconds *SS31 31 1 L 31- 000 es 0 0 9 9** .99 0 6 S S *0 5 0 0* S 0 SO 0* 0 S S S. S OS 0* es. S S 0

*@S

555 *55

S

0 9

SO*

S

Table 1 Zincalloy inqredient (wt Holi -Color Dross Rating Alloy No. Ti I Pb I Cd ICU, Sn, Bi, Sb, In da shd- epsi Holiday Color shadincr Dross deposition Rating Th is invent ion 1 0.25 0 0 0 Acceptable 2 0.25 1.5 o o o Good 3 0.50 1.2 0.1 o o o Good 4 0.30 1.2 0.1 Cu 0.01 o o o Very good 0 .45 CU In Sn 0.02 0.05 0.04 Very good Corn- 6 0.17 1.3 o x 1 0 Unacceptpara- able tive Example 7 0.35 1.1 0.05 x x x Unacceptable o No x Yes U 19 I c-; Using alloys Nos. 2 to 5 of Examples, golden, purple, and blue colors were successfully developed under the following conditions: Golden: Bath temperature 490 0 C (1 min) 4- Holding at 500 0 C for 1 2 seconds Purple: Bath temperature 500 0 C (1 min) 4- Holding at 500 0 C for 10 15 seconds Blue Bath temperature 520 0 C (1 min) Holding at 500 0 C for 15 20 seconds Thus, in the same,manner as in Examples, the oxidation t conditions were gradually intensified to provide a wide variety of colors, as many as six, golden purple too: feI*: blue yellow dark red green, in succession in a controllable way. No holiday or color shading took place.

e0 g* *o Example B 1 (development of dark red color with Tie Mn-Zn alloy) A test piece of steel sheet, SS41, 50 mm wide, 100 mm long, and 3.2 mm thick, was degreased by immersion in an alkaline bath at 80 0 C for 30 minutes. It was washed with so warm water, and then derusted by immersion in a 10 hydrochloric acid bath at ordinary temperature for minutes. Next, the steel sheet was washed with warm water and was fluxed by a dip in a solution containing 35 ZnCl 2

-NH

4 Cl at 60 0 C for 30 seconds.

The steel sheet thus pretreated was plated by immersion in a plating bath of the composition comprising 0.3 wt% Ti 33 20 11 l i 0.1 wt Mn bal. Zn at 580 600°C for one minute. It was pulled out of the bath, held in an oven at 500 520 0 C for 70 seconds, taken out of the oven, and was immediately cooled with warm water at 40 60 0

C.

The steel surface so obtained had a coating of oxide film with a dark red hue.

The test piece of steel sheet with color coating thus obtained was subjected to a salt spray corrosion test for 240 hours. The corrosion weight loss was 60 g/m 2 By way of comparison, ordinary plated steel sheets

S

hot-dip galvanized with distilled zinc were likewise tested.

*e The corrosion weight loss amounted to as much as 120 150 g/m 2 Example B 2 (development of green color with Ti-Mn-Zn alloy) The steel sheet thus pretreated as described was plated by immersion in a plating bath of the composition given below at 600 620°C for one minute. It was pulled out of the bath, held in an oven at 500 5200C for 50 seconds, taken out of the oven, and cooled with warm water by a dip in the bath for 10 seconds.

Composition of the bath: 0.3 wt Ti 0.1 wt Mn bal. Zn.

Zinc used was distilled zinc 1st grade.

The sequential steps of plating, heating, and cooling with warm water gave a uniformly colored coating layer with S- 34 i a bright green hue on the steel sheet.

The test piece of steel sheet with color coating thus obtained was subjected to a salt spray corrosion test for 2 240 hours. The corrosion weight loss was 61 g/m By way of comparison, ordinary steel sheets hot-dip galvanized with distilled zinc were likewise tested. The corrosion weight loss amounted to as much as 120 150 g/m 2 Example B 3 (development of yellow color with Ti-Mn-Zn alloy) Cg The steel sheet pretreated as previously described was plated by immersion in a plating bath of the composition comprising 0.3 wt Ti 0.1 wt Mn bal. Zn at 580 600 C for one minute. It was pulled out of the bath, held

C

•in an oven at 500 520 0 C for 20 30 seconds, taken out of oo the oven, and was immediately cooled by dipping in warm S* owater at 40 600C for 10 seconds.

The steel surface so obtained had a coating of oxide with a bright yellow hue.

The test piece of steel sheet with color coating thus obtained was subjected to a salt spray corrosion test for 240 hours. The corrosion weight loss was 48 g/m 2 By way of comparison, ordinary steel sheets hot-dip galvanized with distilled zinc were likewise tested. The corrosion weight loss amounted to as much as 120 150 g/m 2 Example B 4 (development of blue color with Ti-Mn-Zn I alloy) The steel sheet pretreated as previously described was plated by immersion in a plating bath of the composition comprising 0.3 wt Ti 0.1 wt Mn bal. Zn at 530 550 0 C for one minute. It was pulled out of the bath, allowed to cool in air for 15 25 seconds, and was immediately cooled with water at ordinary temperature.

The steel surface so obtained had a coating of oxide *Oe* film with a uniform blue hue.

"The test piece of steel sheet with color coating thus obtained was subjected to a salt spray corrosion test for Sg/m 2 240 hours. The corrosion weight loss was 70 g/m By way of comparison, ordinary plated steel sheets hot-dip galvanized with distilled zinc were likewise tested.

S.

*The corrosion weight loss amounted to as much as 120 150 g/m 2 Example C (After-treatment) Test pieces of steel sheet, measuring 50 mm wide, 100

S

mm long, and 3.2 mm thick, were either conventionally hotdip galvanized or colored, hot-dip galvanized (with a Zn-Ti alloy). The galvanized pieces were coated with a clear polyurethane resin (resin hardener 5 1) or a colored, aqueous acrylic resin paint by brushing or dipping. The coated pieces, together with uncoated ones, were subjected to outdoor weathering tests. The tests were conducted within a plant under the possession of the present 36 applicant. The degrees of degradation after test periods of three months, six months, and one year were visually inspected. The results are tabulated below in Table 2.

Conventionally hot-dip galvanized pieces became defective in only three months after the painting. Among the colored, hot-dip galvanized pieces, the golden-colored piece had a thinner oxide film than the rest because of the immature oxidation. Without a paint coat, therefore, the golden-colored piece degraded in three months and the blue-colored in one year. Painting could retard the degradation. Needless to say, an increase in the thickness o of the paint coat, multicoating, or other similar step would prove effective in-further retarding the degradation.

o•o 0 37 Table 2 a

S

S. Se 0

S

0 d00~CS

S

S

S

055050 0 5v S 0

S.

S.

6 0 5* S. Sb b 5

S

**SB*S

S

SO OS 5 0 Outdoor weatheriny test Test piece condition 3 months 6 months 1 year Hot-dip Aqueous galvanized x x x acrylic res in Colored Blue o o o galvanized Yellow 0 o o Green C o o Clear Coired Golden o0 x poly- galvanized Blue o 0 0 urethane Yellow o o 0 resin Green 0 0 0 olive o o o Not Colored Golden x x x painted galvanized Blue o 0 A Yellow 0 0 0 Green o o o olive o o o o: Good A: Rather poor X: Poor 38 technology.

25 i f Example D 1 (Spraying) A rod of zinc alloy containing 1.9 wt Ti and 0.3 wt Mn was used as a sprayable material. It was sprayed over a steel material by means of an oxy-acetylene gas flame type spray gun. The sprayed surface was allowed to cool, heated to 500 0 C for 30 seconds, and again allowed to cool in the air.

A green colored coating was obtained.

Example D 2 (Spraying) SUnder the same conditions as in Exarmple 1 but by the 0 use of a zinc alloy rod containing 1.0 wt Ti, spraying and afterheat treatment were carried out.

B

A blue colored coating resulted.

0* 0 *3 3 39 A _L

Claims (8)

1. A zinc alloy for coloured hot-dip galvanising which comprises 0.2-0.7 wt Ti and may or may not further comprise one or more of the following: 1.0-5.9 wt Pb, 0.05-0.2 wt Cd, 0.05-0.15 wt Mn, 0.01-0.05 wt Cu, 0.01-0.05 wt Sn, 0.01-0.05 wt Bi, 0.01-0.05 wt Sb, or 0.01-0.05 wt In, oo. with the balance being Zn and inevitable impurities, wherein said zinc alloy is made from metallic zinc bullion and forms on .0000; a base surface a clear, uniform, brightly coloured coating which adhere well to said base surface.

2. A zinc alloy for coloured hot-dip galvanising which comprises: 0.2-0.7 wt Ti with the balance being Zn and inevitable impurities, wherein said zinc alloy is made from metallic zinc bullion and forms on a base surface a clear, uniform, brightly coloured coating selected from: gold, purple, yellow, dark red and green, which adhere well to said base surface.

3. A zinc alloy for coloured hot-dip galvanising which comprises; 0.2-0.7 wt Ti and 1.3-5.9 wt Pb with the balance being Zn and inevitable impurities, wherein said zinc alloy is TR~1 made from metallic zinc bullion and forms on a base surface a .7 clear, uniform, brightly coloured coating selected from: 40 0185o i i 28 yellow, dark red, green, gold, purple and blue, which adheres well to said base surface.

4. A zinc alloy for coloured hot-dip galvanising which comprises; 0.2-0.7 wt Ti, 1.2-1.3 wt Pb and 0.1-0.2 wt Cd with the balance being Zn and inevitable impurities, wherein said zinc alloy is made from metallic zinc bullion and forms on a base surface a clear, uniform, brightly coloured coating selected from: yellow, dark red, green, gold, purple and blue, whic'. adhere well to said base surface. A zinc alloy for coloured hot-dip galvanising which comprises; 0.2-0.7 wt Ti, 1.0-1.2 wt Pb, 0.05-0.2 wt Cd and 0.01-0.05 wt of at least one element selected from the Sgroup consisting of Cu, Sn, Bi, Sb and In, with the balanc being Zn and inevitable impurities, wherein said zinc alloy is *o* made from metallic zinc bullion and forms on a base surface a clear, uniform, brightly coloured coating selected f-om: yellow, dark red, green, gold, purple and blue, which adhere well to said base surface. **ee

6. A method of forming a coloured zinc coating on an iron or steel surface which comprises the steps of hot-dipping a base metal of iron or steel into a hot-dipping bath of zinc alloy comprising 0.2-0.7 wt Ti, which may or may not further comprise one or more of the following: 1.2-5.9 wt Pb, 0.05-0.2 wt Cd, S0.05-0.15 wt Mn, TR 0.01-0.05 wt Cu, 0.01-0.05 wt Sn, AT O 41 0185o 0.01-0.05 wt Bi, 0.01-0.05 wt Sb, or 0.01-0.05 wt In, with the balance being Zn and inevitable impurities wherein said zinc alloy is made from metallic zinc bullion, at a bath temperature of 450-620 0 C, the coated surface being allowed to cool in air or cooled after heating to a temperature of 450-620 0 C, and thereafter cooled with cold or warm water or with a coolant gas to form on said base metal a clear, uniform, brightly coloured coating which adheres well to said base metal. S., 0 a

7. A method of forming a coloured zinc coating on an iron or :steel surface which comprises the steps of hot-dipping a base Smetal of iron or steel into a hot-dipping bath of zinc alloy comprising; 0.2-0.5 wt Ti, with the balance being Zn and inevitable impurities S wherein said zinc alloy is made from metallic zinc bullion, at a bath temperature of 450-470 0 C, the coated surface being allowed to cool in the air for 5-20 seconds, and thereafter '2 cooled with cold or warm water to form on said base metal a clear, uniform golden coloured coating, which adhere well to said base metal.

8. A method of forming a coloured zinc coating on an iron or steel surface which comprises the steps of hot'-dipping a base metal of iron or steel into a hot-dipping bath of zinc alloy comprising; NT -42 0185o t -i -lr VLY -llilli--____ -X 1_1 0.2-0.5 wt Ti with the balance being Zn and inevitable impurities wherein said zinc alloy is made from metallic zinc bullion, at a bath temperature of 500-550 0 C, either allowing the coated surface to cool in the air for 10-50 seconds or heating it to

500-520 0 C for 10-20 seconds, and thereafter cooling it with cold or warm water to form on said base metal a clear, uniform, purple coloured coating which adhere well to said base metal. 9. A method of forming a coloured zinc coating on an iron or steel surface which comprises the steps of hot-dipping a base g metal of iron or steel into a hot-dipping bath of zinc alloy comprising; S 0.2-0.7 wt Ti, with the balance being Zn and inevitable impurities wherein said zinc alloy is made from metallic zinc bullion, at a bath temperature of 500-620 0 C and the coated surface obtained is cooled or is cooled after heating to a temperature of 450-550 0 C, to form on said base metal a clear, uniform, birghtly coloured coating having a colour selected from: i yellow, dark red and green which is selectively formed on said base metal by controlling the extent of the oxidation of the coating, which adhere well to said base metal. A method of forming a coloured zinc coating on an iron or steel surface which comprises the steps of hot-dipping a base metal of iron or steel into a hot-dipping bath of zinc alloy omprising: 43 0185o L~ mUrCY;l~fP-~;-~Y~ 0.2-0.7 wt Ti, and 1.3-5.9 wt Pb with the balance being Zn and inevitable impurities wherein said zinc alloy is made from metallic zinc bullion, at a bath temperature of 500-620 0 C and the coated surface obtained is cooled after heating to a temperature of 450-550 0 C, to form on said base metal a clear, uniform, brightly coloured coating having a colour selected from: yellow, dark red, gold, purple, blue and green i -lectively formed on said base metal by controlling the extent of the oxidation of the coating, V ,0 which adhere well to said base metal. 0 S11. A method of forming a coloured zinc coating on an iron or 0 steel surface which comprises the steps of hot-dipping a base metal of iron or steel into a hot-dipping bath of zinc alloy comprising; 0.2-0.7 wt Ti, 1.2-1.3 wt Pb and 00.1-0.2 wt Cd with the balance being Zn and inevitable impurities wherein said zinc alloy is made from metallic zinc bullion, at a bath temperature of 500-620 0 C and the coated surface obtained is cooled after heating to a temperature of 450-550 0 C, to form on said base metal a clear uniform, brightly coloured coating having a colour selected from: yellow, dark red, gold, purple, blue and green is selectively formed on said base metal Scontrolling the extent of the oxidation of the coating, 01844 0185o which adhere well to said base metal. 12. A method of forming a coloured zinc coating on an iron or steel surface which comprises the steps of hot-dipping a base metal of iron or steel into a hot-dipping bath of zinc alloy comprising: 0.2-0.7 wt Ti, 1.0-1.2 wt Pb, 0.5-0.2 wt Cd and 0.01-0.05 wt of at least one element selected from the group consisting of Al, Sn, Bl, Sb, and In, with the balance being Zn and inevitable impurities wherein said zinc alloy is made from metallic zinc bullion, at a bath temperature of 500-620 0 C and the coated surface obtained is cooled after heating to a temperature of 450-550 0 C, to form on said base metal a clear, uniform, brightly col, ired coating having a colour selected from: yellow, dark red and green which is selectively formed on said base metal by controlling the extent of the oxidation of the coating, which adhere well to said base metal. 13. A meth-, of forming a coloured zinc coating on an iron or Ssteel surface which comprises the steps of hot-dipping a base metal of iron or steel into a hot-dipping bath of zinc alloy comprising; 0.2-0.5 wt Ti and 0.05-0.15 wt Mn Swith the balance being Zn and inevitable impurities wherein said zinc alloy is made from metallic zinc 0185o I WV"~~~iiv y- Al -i i. I- i i bullion, at a bath temperature of 580-600 0 C, heating the coated work at 500-520 0 C for 30-70 seconds, and thereafter cooling it with water to form on said base metal a clear, uniform a dark red coloured coating, which adheres well to said base metal. 14. A method of forming a coloured zinc coating on an iron or steel surface which comprises the steps of hot-dipping a base metal of iron or steel into a hot-dipping bath of zinc alloy comprising; 0.2-0.5 wt Ti and 0.05-0.15 wt Mn with the balance being Zn and inevitable impurities wherein said zinc alloy is made from metallic zinc bullion, at a bath temperature between 600 and 620 0 C, heating the coated work at 500to 520 0 C for 50 to 60 seconds, and thereafter cooling the same with cold or warm water or with a coolant gas a, to form on said base metal a clear, uniform, green coloured coating, which adheres well to said base metal. 15. A method of forming a coloured zinc coating on an iron or steel surface which comprises the steps of hot-dipping a base metal of iron or steel into a hot-dipping bath of zinc alloy comprising; 0.2-0.5 wt Ti, and 0.05-0.15 wt Mn with the balance being Zn and inevitable impurities Swherein said zinc alloy is made from metallic zinc bullion, r- 46 0185o at a bath temperature between 580-600 0 C, heating the coated work at 500-520 0 C for 20-30 seconds, and thereafter cooling it with cold or warm water or with a coolant gas to form on said base metal a clear uniform, yellow coloured coating, which adhere well to said base metal. 16. A method of forming a coloured zinc coating on an iron or steel surface which comprises the steps of hot-dipping a base metal of iron or steel into a hot-dipping bath of zinc alloy comprising; 0.2-0.5 wt Ti and •l 0.05-0.15 wt Mn with the balance being Zn and inevitable impurities wherein said zinc alloy is made from metallic zinc eo bullion, at a bath temperature of 530-550 0 C, allowing the coated surface to cool in the air for 15-25 seconds, and thereafter cooling it 0 0 with cold or warm water to form on said base metal a clear, uniform blue coloured coating, which adhere well to said base m.tal. 17. A method of forriing a colored zinc coating on an iron or steel surface characterised in spraying a zinc alloy according to any one of claims 1-5, wherein said alloy is in the form of a half-molten sprayabie wire or rod. 18. A method according to any one of the claims 6-17, wherein the colored zinc coating is coated with a paint. 19. A method according to claim 18 wherein the paint is C selected from among synthetic resin paints. A method according to claim 19 wherein the synthetic 47 01850o resin paint is selected from among polyurethane resin, acrylic resin, epoxy resin, and chlorinated rubber paints. 21. A zinc alloy substantially as herein described with reference to any one of Examples A-l to A-3 and B-l to B-4. 22. A method forming a coloured zinc coating substantially as herein described with reference to any one of Examples Al-l to SA-3, B-1 to B-4 and C. 23. Coating iron or steel, whenever coated by the method defined in any one of claims 2 to 16. 0000 DATED this 18th day of December, 1989. °NIPPON MINING CO., LTD NIKKO AEN KABUSHIKI KAISHA By Their Patent Attorneys ARTHUR S. CAVE CO. 48 0185o