CA1259532A - Organic coated steel strip having improved bake hardenability and method for making - Google Patents

Abstract

ABSTRACT OF THE DISCLOSURE
An organic coated steel strip having improved bake hardenability is provided which comprises an extra low carbon steel substrate having bake hardenability, a zinc alloy layer deposited on the substrate in a weight of 10 to 40 g/m2, a chromate layer formed on the zinc alloy layer in a weight of at least 10 mg/m2 of metallic chromium, and an organic coating, optionally containing silica, attached to the chromate layer. The coated strip is prepared by depositing a zinc alloy on an extra low carbon steel substrate, subjecting the substrate to a chromate treatment in an aqueous chromate solution containing a chromate compound, a reducing agent, and an acid residue, resin or silica, and applying an organic coating on the chromate layer and baking the coating at a temperature of up to 150°C.

Description

~2~953~

Kobayashi et al TITLE OF THE INVENTION
Organic Coa~ed Steel Strip Having Improved Bake Hardenability and Method for Making BACKGROUND OF THE INVENTION
This invention relates to corrosion resistant, organic coated steel strips having improved bake hardenability and drawability and finding application in automobiles.
As often encountered in the manufacture of automobiles, strip steel is pressed formed to a desired shape and then coated with a protective coating typically by electrophoretic painting followed by baking at elevated temperatures. The term bake hardenability designates that the strip steel hardens during the baking of such a coating.
Usually, the bake hardenability of strip steel is evaluated in terms of an increase of yield strength by baking a 2%
pre-stressed, steel stxip at 170C for 20 minutes and measuring the yield strength.
In these years, there exists a greater demand for further improving the corrosion resistance of automotive strip steel. A number of rust-preventive steel strips have been proposed to meet such a demand and many of them are successfully used. These rust- or corrosion~preventive steel strips are surface treated steel strips including ~inc and ZillC alloy hot dl~pec1 steal, ZillC ~n~ zine alloy electroplated, and zinc rlch painted, typically organic zinc rich painted steel strips. In addition, composite coated steel strip have also been developed wherein a plated steel strip is covered with an organic coating. These composite coated steel strips are known to be the currently rnost improved corrosion-preventive steel strips.
For energy saving and drivability improvernent, an increasing amo~nt of high tensile strip steel has been used

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in the manufacture of automobiles. To compensate for the loss of dent resistance resulting from thickness reduction, desired is a steel strip which exhibits a low yield strength prior to press forming and increases its yield stren~th during paint baking. Also in common drawing steel strips, bake hardening after press forming is a phenomenon favourable for increasing dent resistance particularly when the strips are used as automobile outer plates.
Steel strips are thus desired to have both deep drawability and bake hardenability.
10Thus, there is a need for corrosion-preventiv~ steel strips capable of satisfying not only corrosion resistance, but also a variety of re~uirements such as light weight, safety and rigidity.
One conventional commercially available steel meeting such consideration is a class of zinc and zinc alloy plated steel strips 15having bake hardenability. An organic coating is applied to a zinc or zinc alloy plated steel strip. The organic coating on the steel must be baked at a temperature of higher than 150C in order to convert it into a hardened one. Thus the organic coated steel strip has been hardened prior to press forming and is thus not 20amenable to drawing.
More particularly, some of conventional automotive organic coated or painted steel strips are known under the trademark of ~incrometal (Diamond Shamrock) as disclosed in Canadian Patents Nos. 863,894, 918,516, 940,427, 9~3,442, 962,923, 970,668, and 25979,337, and some are disclosed in Canadian Patent No. 1,200,723, U.S. Patent No. 4,659,39~, and Japanese Kokai (laid open applications) Nos. 60-86281 and 60-105535. All these coated strips suffer from the above-mentioned problem because they must be baked at a temperature in excess oE 150C in order to convert the organic 30coating into a hardened one. The bake hardenabiLity o~' ~te~l substrates themselve~ could not be b~neelciaLLy utilized.

SUMM~ OF TH~ INV~N~IQ~
An object of the present invention is to provide a novel and improved organic coated steel strip which exhibits bake _ 3 _ 12,S~3~

hardenability and good workabili~y even after baking of the organic coating.
Another object of the present inven~ion is to provide a method for making such an organic coated steel strip.
A further object of the present invention is to provide a method for making an organic coated steel strip having improved bake hardenability and capable of maintaining a high proportion of chromium fixed while preventing chromium from being dissolved out during alkaline degreasing and/or chemical conversion as used in an automotive coating process.
According to a broad aspect of the present invention, there is provided a method for making an organic coated steel strip having improved bake hardenability of 3.5 to 6.1 kgf/mm2, comprising the steps of: depositing a layer of a zinc base alloy on one surface of an extra low carbon steel substrate containing 0.001 to 0.008 weight percent carbon and having bake hardenability in a weight of 10 to 40 g/m2, subjecting said substrate to a chromate treatment to form a chromate layer on the zinc base alloy layer in a weight of at least 10 mg/m2 calculated as metallic chromium, and applying an organic coating on the chromate layer and baking the coating at a tempe:rature of up to 150C.
In a further broad aspect the present invention relates to a method for making an organic coated steel strip having improved bake hardenability of 3.5 to 6.1 kgf/mm2, comprising the steps of:
depositing a layer of a zinc base alloy on one surface of an extra low carbon steel substrate containing 0.001 to 0.008 weight percent carbon and having bake hardenability, subjecting said substrate to a chromate treatment to form a chromate layer on the zi.nc base alloy layer, and applying an organic coating on the chromate layer and baking the coating at a temperature o~ up to 150C, wherein ~aid chromate treatment uses ~n a~ueou~ cllromate ~olution containing a chromate compound, a reducing agent, and at least one member selected from acid residues, resins and silica.

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_RIEF DESCRIPTION OE' THE DRAWINGS
In order that those skilled in the art will readily understand the practice of the present invention, the following description is made with reference to the accompanying drawings, in which:
5FIG. l is a diagram showing a stable chromium fixing region in relation to baking temperature and Cr6+/Cr3~;
FIG. 2 is a diagram showing a chromium fixing proportion as a function of the amount of methanol added to a chromate solution;
FIG. 3 is a diagram showing a chromium fixing proportion as 10a function of the amount of phosphoric acid added to a chromate solution;
FIG. 4 is a diagram showing a chromium fixing proportion as a function of the amount of a resin added to a chromate solution;
FIG. 5 is a diagram showing a chromium fixing proportion as 15a function of the amount of silica added to a chromate solution;
and FIG. 6 is a diagram showing the bake hardenability expressed in BH value of steel strip as a function of the baking temperature of organic coating.

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DE ILED DESCRIPTION OF THE INVENTION
The present invention pro~ides a highly corrosion resistant, organic coated steel strip capable of maintaining improved bake hardenability after press forming, which is prepared by preparing a drawing extra 'ow carbon steel substrate having bake hardenability, depositing a layer of a zinc base alloy on one surface of the substrate, subjecting said substrate to a chromate treatment to form a chromate layer on the zinc base alloy layer, and applying an organic coating on the chromate layer and baking the coating at a temperature of up to 150C.
As previously described, automotive organic coated or painted steel strips must be baked at a temperature in excess of 150C in order to convert the organic coating into hardened one.
The reason is that in case of ZincrometalR with which cold rolled steel is coated, for example, baking must be effected at a sufficiently high temperature to cause the powder zinc-containing chromate to react with the steel substrate. The use of a high-boiling solvent to dissolve a high molecular weight resin also requires a baking treatment at a temperature of higher than 150C.
A si.milar requirement is imposed on plated steel strips, for example, composite zinc rich/organic coated steel strips as disclosed in Canadian Patent No. 1,200,723. That is, baking of the organic coating must be at a high temperature as encountered for the cold rolled steel mentioned above.
Also, steel strips having a thin film organic coating other than the zinc rich paint are baked at a high temperature because a binding agent capable of crosslinking at a high temperature, for example, melamine resin must be added in the state o~` the a~t.
For all these convent:i.ona:l. o~ganic coatLng~, .Lt I.s not contemplated to take a~vclntclge of the bake hardenability of ``~

~25~32 strip steel as done ln the present invention. Therefore, the conventional coated strips have poor workability.
In order to take advantaye of the bake hardenability of strip steel while maintaining the corrosion resistance as available with ~onventional coatings, we have investigated the organic coating which can exhibit sufficient corrosion resistance even when baked at a temperature of 150C or lower. We have discovered that when a cold rolled substrate of extra low carbon steel having bake hardenability by nature is provided with an organic corrosion-preventive coating by a baking treatment at a temperature of up to 150~C so as not to lose the inherent bake hardenability, there is available an optimum range of overall coating consisting of plating plus pre-treatment plus organic coating in which the organic corrosion-preventi~e coating can provide corrosion resistance, workability and weldability equal or superior to those of conventional highly corrosion resistant organic coated or painted steel strips.
Therefore, the present invention provides an organic coated steel strip having improved bake hardenability, comprising an extra low carbon steel substrate having bake hardenability, a layer of a zinc base alloy deposited on one surface of said substrate in a weight of 10 to 40 g/m2, a chromate layer formed on said zinc base alloy layer in a weight of at least 10 mg/m2 calculated as metallic chromium, and an organic coating, optionally containlng silica, attached to said chromate laye~ b~ baking at a tempe~ature of up to 150C.
According to the present invention, the temperature at which the organic coating is baked is limited to 150C or lower in order to maintain the bake hardenability. The reason will become clear from the description of a series of experiments.

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The starting steel was an extra low carbon steel consisting of, in percentage by weight, 0.003% C, 0.01~ Si~
0.16% Mn, 0.04~ Al, 0.070% P, 0.026% Nb and balance essentially ~e. The strip steel was cold rolled at a draft of 80% to a thickness of 0.7 mm, heat treated by soaking at 850C for 30 seconds and cooled to 650C at a rate of ~5C/sec. in a continuous annealing furnace, and then skin pass rolled at a draft of 1.0%. The resulting extra low carbon steel strip having bake hardenability was determined for mechanical properties, exhibiting a yield strength (YS~
of 20 kgf/mm2, a tensile strength (TS~ of 35 kgf/mm2, an elongation (El) of 45~, and a bake hardenability (BH) of 5 kgf/mm2. As previously defined, BH is equal to YS of baked strip minus YS of initial strip.
An organic coating was applied to the steel strip and baked at various temperatures for one minute. The bake hardenability of the baked steel strip is shown in FIG. 6 as a function of the baking temperature. As seen from the curve in FIG. 6, the steel strip experiences a sudden drop in BH value when the baking temperature exceeds 150C, losing the inherent bake hardenability.
The preferred cold rolled steel strips having bake hardenability with which the present invention starts are bake hardenable, cold rolled steel strips comprising, in percentage by weight, 0.001 to 0.008% of C, up to 0.5% of Si, 0.05 to 1.2% of Mn, up to 0.1~ of P, 0~01 to o.oa~ 0f Al, the aluminum b~ing at le~st ~3 tlmes the perce~t N, from

3 times the percant C to ~ tim0s th~ pe.rcent C plus 0.02~ of Nb, up to 0.05~ of Ti, and balance essentially Fe, the strips being continuously annealed to have a BE1 value of 3 to 6 kgf/mm2. The extra low carbon steel materials tlndergo little hardening dl~ring mild baking at temperatures of 150C
or lower so that they maintain their own bake hardenability.
Although the reason is not exactly understood, it is expected that bake hardenable steel strips of extra low ~9~3;2 carbon steel and those of low carbon steel have a different distribution of C in solid solution form within grains even though both have the same apparent sH value.
In the extra low carbon steels previously defined as providing the preferred bake hardenable cold rolled steel strips, the contents of the respective elements are limited to certain ranges.
Carbon, C preferably ranges from 0.001 to 0.008 wt%.
Contents of less than 0.001 wt% lead to the loss of the solid solution carbon contributing to bake hardening.
Steels having more than 0.008 wt% of carbon exhibit too high yield strength and low ductility and r value (Lankford value).
Silicon, Si preferably ranges up to 0.5 wt%. In excess of 0.5 wt%, an oxide film will form to detract from chemical conversion amenability.
Manganese, Mn preferably ranges from 0.05 to 1.2 wt%.
Red shortness diminishes at less than 0.05 wt% whereas r value is reduced in excess of 1.2 wt%.
Phosphorus, ~ preferably ranges up to 0.1 wt%. Steel becomes brittle with P contents in excess of 0.1 wt%.
Aluminum, Al preferably ranges from 0.01 to 0.08 wt%
and at least 8 times the percent N. At least 0.01 wt% of Al is necessary to fix nitrogen. Al contents of more than 0.08 wt% undesirably generate many inclusions. The function of Al to fix nitrogen provides the additional requirement that its content be at least 8 timeC3 the perc0nt N~
Niobium, N~ preferabl~ ranyes ~rom 3 tlmes the percent C to 8 times the percent C plus 0.02~. Below the lower limit of 3 times the percent C, a too lar~er amount of solid solution carbon is left, inhibiting the formation of an aggregate structure contributing to drawability during cold rolling recrystallization. Ductility is impaired in excess of 8 times the percent C plus 0.02%.

~595~2 Titanium, Ti preferably ranges up to 0.05 wt~ because the bake hardenability of steel is lost in excess of this limit.
The steel strips are preferably controlled to a BH
value of 3 to 6 kgf/mm2. A value of less than 3 kgf/mm2 is a substantial loss of bake hardenability. Steels having BH
values in excess of 6 kgf/mm2 undergo severe deterioration upon aging and stretcher strain during working.
The extra low carbon steel strips are plated with zinc based alloys by any known deposition techniques, typical electrodeposition. Some non-limiting examples of the zinc base alloy platings include Zn-Ni alloy platings preferably having a nickel content of 5 to 13 wt~; Zn-Fe alloy plating preferably having an iron content of 8 to 25 wt%; Zn-Co-Al2O3-Cr2O3 alloy platings preferably having a cobalt content of 1 to 5 wt%; Zn-Al alloy platings preferably having an aluminum content of 1 to 15 wt%; Zn-Ni/Fe-P
double-layered alloy platings preferably having a phosphorus content of 0.0003 to 5~ by weight based on the weight of Fe-P; Zn-Fe/Fe-P double-layered alloy platings preferably having a phosphorus content of 0~0003 to 5% by weight based on the weight of Fe-P. These zinc base alloy platings which have corrosion resistance several times higher than the conventional pure zinc plating are effective in achieving the objects of the present inventi~n. The amount of zinc alloy plated, that is, plating weight should range from 10 to 40 gram per square meter (g/m2). Corrosion resistance is insufficient with less than 10 g/m2 whereas plating weights in excess of 40 g/m2 provide no additional benefit in corrosion resistance improvement and are thus uneconomical.
In the above-listed zinc base alloys, the contents of the respective elements are preferably limited to certain ranges.
The Zn-Ni alloys preferably have a nickel content of 5 to 13 wt%. ~ess than 5 wt% of Ni provides insufficient corrosion resistance whereas a plating containing more than 13 wt% of Ni is too hard.
The Zn-Fe alloys preferably have an iron content of 8 to 25 wt%. Less than 8 wt% of Fe provides insufficient corrosion resistance whereas red rust will often generate in excess of 25 wt~ of Fe.
The Zn-Co-A12O3-Cr2O3 alloys preferably have a cobalt content of 1 to 5 wt%. Less than 1 wt% of Co provides insufficient corrosion resistance whereas more than 5 wt% of Co is uneconomical.
The Zn-Al alloys preferably have an aluminum content of 1 to 15 wt%. Less than 1 wt% of Al provides insufficient corrosion resistance whereas sacrificial corrosion prevention is lost in excess of 15 wt% of Al.
The Fe-P alloys for the double-layered Zn-Ni/Fe-P and Zn-Fe/Fe-P platings preferably have a phosphorus content of 0.0003 to 5% by weight based on the weight of Fe-P.
Platings having less than 0.0003 wt% of P are less susceptible to chemical conversion. More than 5 wt% of P is uneconomical because of reduced current efficiency during plating process.
The zinc base alloy platings are subjected to a chromate treatment in order to improve their adherence to subsequently applied organic coatings and hence, the corrosion resistance of the overall structure. The chromate treatment is carried out to produce a chromate film of at least 10 mg/m2 of metallic chromium. Either coating or electrolytic chromate treatment is advantageous in controlling the amount of chromate film to such a level.
Chromate films of less than 10 mg/m2 of metallic chromium have insufficient corrosion resistance and poor adherence to the subsequently applied organic coatings.
On the chromate layer thus formed is applied an organic coating which is baked at a temperature of up to 150C and assists in improving corrosion prevention. The ~59532 organic coating compositions used in the practice of the present invention contain as a main ingredient, a resin selected from the following three groups:
(1) water dispersible resins including acrylic, polyethylene, epoxy, and alkyd resins and modified ones thereof;
(2) solvent type resins including epoxy and polyester resins and modified ones thereof; and (3) UV- or electron radiation-curable resins such as acrylic, epoxy, and polyurethane resins, alone or a mixture thereof.
When resin (1) or (2) listed above is used, there are contemplated some methods for assisting in fully hardening the resin by a heat treatment at a low temperature of up to 150C, for example, the use of low temperature curing agents, for example, metal salt catalysts such as cobalt naphthenate, optionally in combination with amine curing agents such as diethylene triamine. With these curing agents added, the curing process can proceed at room temperature. An organic coating may be more readily formed by using a method adequate for the particular type of organic resin used. Examples of the curing agents which exert their function upon heating include urea resins, melamine resins, benzoguanamine resins, block isocyanate resins, and phenol resins.
Known examples of UV- or electron radiation-curable resins (3) are acrylic resin coatings utilizing a benzoin ether as a photopolymerization initiator and epoxy resin coatings utilizing an aromatic diazonium salt as a photopolymerization initiator. Exemplary of the resins having an electron radiation-curable functional group there may be given acrylic and epoxy resins utilizing epoxy-acid addition reaction and polyurethane resins utilizing isocyanate-hydrogen group addition reaction. These resins (3) can advantageously maintain the bake hardenability of 1259S~2 the steel substrate substantially unchanged because they can be baked at temperatures of several ten degree in Centigrade.
The resinous coating composition of any of resins (1) to (3~ is applied to the chromate layer to a thickness of 0.5 to 3 ~m. Organic coatings of less than 0.5 ~m thick provide insufficient corrosion resistance whereas more than 3 ~m thickness adversely affects weldability.
The resinous coating composition may further contain up to 60% by weight of silica sol for the purpose of improving corrosion resistance. Coating compositions containing more than ~0% by weight of silica sol are too viscous and tend to gel.

The composite coated steel strips mentioned above are improved rust-preventive steel strips. As previously mentioned, a chromate treatment is often employed as a preliminary treatment for the organic coating in order to enhance corrosion resistance. A usual automotive part coating process proceeds according to the scheme of blank (organic coated steel) - assembly - alkaline degreasing -chemical conversion - electrophoretic deposition -intermediate coating - top coating. Since the temperature at which the chromate and resin films are baked is controlled relatively low to maintain bake hardenability according to the present invention, there is the likelihood that when a conventional chromate solution is used in the preliminary treatment, chromium be dissolved out during the alkaline degreasing and chemical conversion, imposing a problem to spent liquid disposal.
We have found that in alkaline degreasing of an automotive steel strip comprising a zinc alloy-plated steel substrate which has been subjected to a chromate treatment and an organic coating treatment, the chromium can be 1'~5!:~S32 dissolved out so that the degreased steel strip has only a markedly reduced amount of chromate attached thereto.
To overcome this drawback, we have studied the addition of reducing agents, acids, resins, and silica to the chromate solution, and arrived at the method of the present invention.
Therefore, the present invention according to the other aspect provides a method for making an organic coated steel strip having improved bake hardenability, comprising the steps of:
preparing an extra low carbon steel substrate having bake hardenability, depositing a layer of a zinc base alloy on one surface of the substratej preferably in a weight of 10 to 40 g/m2, subjecting said substrate to a chromate treatment to form a chromate layer on the zinc base alloy layer, preferably in a weight of at least 10 mg/m2 calculated as metallic chromium, the chromate treatment using an aqueous chromate solution containing a chromate compound, a reducing agent, and at least one member selected from acid residues, resins and silica, and applying an organic coating on the chromate layer and baking the coating at a temperature of up to 150~C.
The organic coated steel strips produced by the method of the present invention experience controlled dissolving out of chromium during alkaline d~greasing and/or chemical conversion in the automotive coating process without a loss of corrosion resistance.
The chromate treatment will be described in more detail. We have made an experiment to examine the proportion of chromium fixed during alkaline degreasing and/or chemical conversion in the automotive coating process. The starting steel strip is an extra low carbon steel consisting of, in percentage by weight, 0.003~ C, 0.01% Si, 0.16% Mn, 0.04% Al, 0.070% P, O.G26% Nb, and 1~59532 balance essentially Fe. A zinc base alloy, typically Zn-Ni alloy was plated on the strip in a plating weight of 10 to 40 g/m2, a chromate solution having a ratio of hexavalent to trivalent chromium (Cr6+/Cr3+) of from 80/20 to 20/80 was applied and baked to the zinc base plating, and then a resin in water or solvent, typically epoxy resin was applied and baked to the chromate film. It is to be noted that the ratio of Cr6+/Cr3+ was measured by the redox titration technique. The maximum temperature to which the strip was heated was from room temperature to 150C for both the chromate and resin film baking steps.
When a conventional chromate solution, that is, free of any additives as defined in the present invention, is used, higher temperatures at which the applied chromate and resin films are baked cause more hexavalent chromium to be reduced to trivalent chromium, resulting in an increased chromium fixing proportion. For example, when the films were baked at temperatures of higher than 150C, the percent of chromium remaining fixed after alkaline degreasing was at least 80%, which level is acceptable in the automotive coating process. With attention paid to the steel substrate, however, yield strains are induced therein during the process. There arise some problems including removal of such yield strain as well as increased yield stress and deteriorated press formability.
Therefore, it is intended in the present invention to improve the percent chromium fixed, provided that the maximum baking temperature is limited to the range between room temperature and 150C.
According to one embodiment of the present invention, chromate solutions having added thereto methanol as a reducing agent and phosphoric acid as an acid residue was applied and baked to plated steel strips at temperatures of from room temperature to 150C and then a resin was applied and baked to the chromate film at a temperature of from room ~259S32 temperature to 150C. The chromium fixing proportion, that is, percent chromium fixed of the strips was plotted in FIG.
1 as a function of the Cr6+/Cr3+ ratio of the chromate solution and the maximum baking temperature. The range of Cr6+/Cr3+ ratio within which the percent chromium fixed is 80~ or higher is depicted hatched as a favorable region in FIG. 1. Although the reducing agent used is methanol and the additive used is phosphoric acid, similar results are obtained when other reducing agents are used and/or other additives such as acids other than phosphoric acid, resins and silica are used.
To achieve a favorable percent chromium fixed of 80%
or higher with the maximum baking temperature ranging from room temperature to 150~C as shown in FIG. 1, we have found that favorable results are obtained by adding a reducing agent and at least one additive selected from acid residues, resins, and silica to the chromate solution.
Examples of the reducing agents added to the chromate solution include methanol, aqueous hydrogen peroxide, ethylene glycol, succinic acid, succinimide, but are not limited thereto. The reducing agent is added in an amount sufficient to provide a RAH of 0.2 to 1.9 per gram molecule of CxO3. The term RAH is the gram atoms of hydrogen contained in the reducing agent. With RAH of less than 0.2, the percent chromium fixed is reduced to an unacceptable level even when the additive as defined below is additionally used. The chromate solution becomes gel if RAH
is above 1.9.
The additive which is used in the chromate solution in combination with the reducing agent are selected from acid residues, resins, and silica. They are described in more detail.
(1) Acid residues Preferred acid residuex are provided by such acids as phosphoric acid and boric acid. They are added in an amount . ~

~5953~

to give a A X/CrO3 ratio of from 0.05 to 0.3 by weight wherein A x represents an acid residue. Ratios of less than 0.05 will result in a percent chromium fixed of less than 80% whereas ratios of more than 0.3 will result in poor corrosion resistance.
(2) Resins Preferred examples of the resins added to the chromate solution include acrylic resins having an acid value of at least 250 and acrylic resins having acrylic acid monomer 1G and/or methacrylic acid monomer added to stabilize them.
They are added in an amount to give a resin/CrO3 ratio of from 0.1 to 20 by weight. Ratios of less than 0.1 will result in a percent chromium fixed of less than 80% whereas ratios of more than 20 will deteriorate the adherence of the chromate film to the underlying substrate.
~3) Silica Silica added to the chromate solution is preferably colloidal silica. Silica is added in an amount to give a SiO2/CrO3 ratio of from 0.3 to 3.0 by weight. Ratios of less than 0.3 will result in a percent chromium fixed of less than 80% whereas ratios of more than 3.0 will deteriorate the adherence of the chromate film to the underlying substrate.
When a steel strip carries a chromate film resulting from the chromate solution having added the reducing agent and the additive as defined above, the steel can maintain a significantly high percent chromium fixed at the end of alkaline degreasing and chemical conversion in the automotive coating process. To demonstrate the maintenance of high percent chromium fixed, an experiment was made us-ng an immersion type alkaline degreasing solution commonly used in the automotive coating process.
FIG. 2 graphically shows the percent chromium fixed as a function of the amount of methanol added as the reducing agent. It is seen that only the addition of methanol, that ~Z59532 is, reducing agent mostly results in a percent chromium fixed of less than 80~. However, the RAH/CrO3 ratio range from 0.2 to 1.9 gives a ratio of Cr6+/Cr3+ in the range of from 80/20 to 20/80. Then, the percent chromium fixed can be 80% or higher as seen from FIG. 1 by adding at least one additive selected from (1) acid residues, (2) resins, and (3) silica to the chromate solution while keeping the maximum baking temperature within the range of from room temperature to 150C.
FIG. 3 graphically shows the percent chromium fixed as a function of the amount of phosphoric acid added as producing an acid residue to the chromate solution having methanol added as the reducing agent (RAH/CrO3=1.0). It is seen that when the amount of phosphoric acid added is at least 0.1 calculated as PO43 /CrO3, a percent chromium fixed of 100% is advantageously achieved even at a ratio of Cr6+/Cr3+ of 80/20. It is also seen that when the ratio of Cr6+/Cr3+ is 20/80, a percent chromium fixed of 100% is advantageously achieved even at a ratio of PO43 /CrO3 of 0.01. When phosphoric acid is added in an amount to give a PO43 /CrO3 ratio of 0.3 or higher, the phosphoric acid due to its non-volatile nature adversely affects the subsequently applied and baked resin and hence, the corrosion resistance of the product.
FIG. 4 graphically shows the percent chromium fixed as a function of the amount of a resin added to the chromate solution having methanol added as the reducing agent (RAH/CrO3=1.0~. The resin used is an acidic acrylic resin.
The amount of resin added is expressed as a weight ratio of resin solids/CrO3. It is seen that a resin solids/CrO3 ratio in the range beween 0.1 and 20.0 is effective in improving the percent chromium fixed. Such a ratio of more than 20.0 adversely affects the adherence of chromate film to the underlying substrate, and hence, the workability and weldability of the product.
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FIG. 5 graphically shows the percent chromium fixed as a function of the amount of silica added to the chromate solution having methanol added as the reducing agent (~AH/CrO3=1.0). The silica used is ultrafine particulate silica anhydride.
The amount of silica added is expressed as a weight ratio of SiO2/CrO3. It is seen that a SiO2/CrO3 ratio of at least 0.3 is effective in achieving a percent chromium fixed of 80~ or higher. Such a ratio of more than 3.0 adversely affects the adherence of chromate film to the underlying substrate, and hence, the weldability of the product.
The foregoing experimental results indicate that the addition of a reducing agent in combination with (1) an acid residue, (2) a resin or (3) silica to the chromate solution is effective in increasing the percent chromium fixed at the end of alkaline degreasing in the automotive coating process. The additive effects of these agents are estimated as follows.
The reducing agent such as methanol, aqueous hydrogen peroxide and ethylene glycol is added to the chromate solution. The reducing agent reduces chromic acid to lower the Cr6+/Cr3+ ratio. The percent chromium fixed is then increased because the proportion of hexavalent chromium which is more liable to dissolve away is decreased.
The additives, (1) acid residue, (2) resin, and (3) silica added to the chromate solution have the following functions.
(1) Addition of acid residue to chromate solution Two sets of samples were prepared by applying a chromate solution having phosphoric acid residue added and an acid residue-free chromate solution followed by baking.
Analysis of the samples from the acid residue-containing chromate solution indicates peaks probably attributable to the hydrate or hydroxide of trivalent chromium in addition to the peaks of trivalent and hexavalent chromium. No 1~59~

substantial difference is observed in the proportion of he~avalent chromium between the acid residue-introduced and free solutions. When the chromate films are evaluated as applied, the percent chromium fixed does not depend on the introduction of acid residue. However, when a resin is subsequently applied and baked to the chromate films, the hydrate or hydroxide of trivalent chromium is firmly attached to the resin, eventually preventing hexavalent chromium from dissolving out. It has also been observed that hexavalent chromium itself reacts with the resin to reduce its quantity. These two mechanisms decrease the dissolving out of hexavalent chromium.
(2) Addition of resin to chromate solution When the chromate solution contains an acrylic resin or a similar resin which is of acidic type and stable in the chromate solution, the Cr6+/Cr3+ ratio of the solution remains unchanged, but a bond is created between hexavelent chromium and the resin at the end of baking to prevent the hexavalent chromium from dissolving out.
(3) Addition of silica to chromate solution When a chromate film is used alone without subsequent resin coating, the percent chromium fixed decreases with the increasing amount of silica added to the chromate solution.
Analysis of silica-containing chromate films indicates more OH groups than in silica-free chromate films. The distribution of silicon in the chromate film is also determined to find that Si is concentrated in a surface layer.
These indicate that silica forms a rigid film at the surface layer of the chromate film in which the chromate itself is present as the hydrate and hydroxide of trivalent chromium. When a resin is subsequently applied and baked to such a chromate film, the resin is firmly attached to the O~
group of the chromate film so that the resulting resin-~2sss3~

coated steel strip is characte~ized by the controlled dissolving-out of chromium.

EXAMPLES
Examples of the present invention are given below by way of illustration and not by way of limitation.
Example 1 The composition of cold rolled steel strips having bake hardenability used in a series of runs is shown in Table 1 together with their mechanical properties.
Using bake hardenable steel strips, blank Nos. 1-6 as shown in Table 1, test specimens were prepared by depositing a zinc base alloy plating on the blank, subjecting the plating to a chromate treatment, and then applying an organic coating followed by baking. The treating procedure is shown in Table 2.
The test specimens were determined for corrosion resistance, weldability, workability, and bake hardenability, with the results shown in Table 3.
The tests are conducted by the following procedures.
1. Corrosion Resistance 1-a) Salt spray test (SST) A salt spray test was carried out by crosshatching the organic coating on each specimen, and spraying a 5% NaCl solution at 35C to the coating. The time was observed until red rust generated.
1-b) Cycle corrosion test (CCT) A cycle corrosion test was carried out by subjecting each specimen to corrosion cycles each consistiny of spraying of 5% NaCl at 35C for 4 hours, drying at 60C for 2 hours, and allowing to stand in wet conditions at 50C, RH
95% for 2 hours. The number of cycles was counted until red rust generated.
2. Weldability 125953~

Two pieces of each specimen were partially overlapped and subjected to continuous spot we]ding using an R type electrode (40R) each under a compresslon force of 170 kg for a welding period of 10 cycles (50Hz, 1/5 sec). The number of permissible continuous welding spots was determined.
3. Workability Each specimen in a disk form having a diameter of 90 mm was subjected to a cupping test by drawing to a cup shape having a diameter of 50 mm and a depth of 25 mm (Blank Hold 1Q Force 1 Ton). An adhesive tape was applied to and removed from the worked area to determine the removal of coating as expressed in mg/circumference.

4. Bake Hardenability Each specimen was pre-stressed 2% and then subjected to a baking treatment at 170C for 20 minutes. The yield strength (YS) of the specimen was measured to determine an increase of YS in kgf¦mm2.
The data in Table 3 demonstrate that the organic coated steel strips obtained according to the present invention have high corrosion resistance, good weldability and workability while maintaining satisfactory bake hardenability.

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Table 3 (cont'd) Corrosion resistance Weld- Workability BH
Blank SST CCT ability ~mg/circum- (kYf2 No. (hour) (cycle) (spots) ference) /mm ) Invention F-l ~ >2500 >200 >1000 <1 5.0 F-2 6>2500>200 >1000 <1 5.0 F-3 >2500 >200 >1000 <1 5.0 Comparative G-l 1000 100 >1000 <1 4.5 runs G-2 1500 100 >1000 <1 4.5 G-3 1>2000>150 700 1-2 4.5 G-4 >2000 >150 500 1-2 4.5 G-5 >2000 >150 300 1-2 4.5 H 1>2000>150 500 60 0 I 1>2000>150 >1000 10 0 J 1>2000>150 >1000 5 0 ~259~:i3':' Example 2 The cold rolled steel strips having bake hardenability used were the same as used in Example 1. Their compositions are shown in Table 1 together with their mechanical properties.
Using bake hardenable steel strips, blank ~os. 1-6 as shown in Table 1, test specimens were prepared by depositing a zinc base alloy plating on the blank, subjecting the plating to a chromate treatment, and then applying an organic coating followed by baking. The treating procedure is shown in Table 4.
The test specimens were determined for corrosion resistance, weldability, workability, bake hardenability, and percent chromium fixed, with the results shown in Table

5.
The procedures for measuring the former four properties are the same as in Example 1.
Percent chromium fixed was determined by degreasing a specimen with a commonly used immersing alkaline degreasing solution. Using fluorescent X-ray analysis, the number of chromium counts was determined before and after the alkaline degreasing.
The data in Table 5 demonstrate that the organic coated steel strips produced according to the method of the G5 present invention have high corrosion resistance, good weldability and workability while maintaining satisfactory bake hardenability and high percent chromium fixed.

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Blank SST CCT ability (mg/circum- (kgf2 Cr No. (hour) (cycle) (spots) ference) /mm ) fixed Invention A-l >2500 >200 >lO00 <l 4.6 >90 A-2 >2500 >200 >lO00 <l 4.7 >90 A-3 >2500 >200 >lO00 <l 4.3 >90 A-4 >2500 >200 >lO00 <l 4.4 >90 A-5 l >2500 >200 >lO00 <l 4.4 >90 A-6 >2500 >200 >lO00 <l 4.4 >90 A-7 >2500 >200 >lO00 <l 4.4 >90 A-8 >2500 >200 >lO00 <l 4.4 >90 A-9 , >2500 >200 >lO00 <l 4.4 >90 B-l ~ >2500 >200 >lO00 <l 4.7 >90 B-2 ¦ >2500 >200 >lO00 <l 4.5 >90 B-3 ~2 >2500 >200 >lO00 <l 4.7 >90 B-4 J >2500 >200 >lO00 <l 4.5 >90 C-l ~ I >2500 >200 >lO00 <l 4.5 >90 C-2 >2500 >200 >lO00 <l 4.5 >90 C-3 >2500 >200 >lO00 <l 4.5 >90 C-4 3 >2500 >200 >lO00 <l 4.3 >90 C-5 1 >2500 >200 >lO00 <l 4.5 >90 C-6 ~ >2500 >200 >lO00 <l 4.5 >90 D-l >2500 >200 >lO00 <l 4.5 >90 D-2 4 >2500 >200 >lO00 <l 4.5 >90 D-3 >2500 >200 >lO00 <l 4.5 >90 E-l 1 >2500 >200 >lO00 <l 4.7 >90 E-2 >2500 >200 >lO00 <l 4.7 >90 E-3 5 >2500 >200 >lO00 <l 4.7 >90 E-4 >2500 >200 >lO00 <l 4.5 >90 F-l 1 >2500 >200 >lO00 <l 4.5 >90 F-2 >2500 >200 >lO00 <l 4.5 >90 F-3 6 >2500 >200 >lO00 <l 4.7 >90 F-4 ~ >2500 >200 >lO00 <l 4.7 >90 ~ ~5~'3S3~

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Claims (14)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE PROPERTY OR
PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:

1. An organic coated steel strip having improved bake hardenability of 3.5 to 6.1 kgf/mm2, comprising an extra low carbon steel substrate containing 0.001 to 0.008 weight percent carbon and having bake hardenability, a layer of a zinc base alloy deposited on one surface of said substrate in a weight of 10 to 40 g/m2, a chromate layer formed on said zinc base alloy layer in a weight of at least 10 mg/m2 calculated as metallic chromium, and an organic coating attached to said chromate layer by baking at a temperature of up to 150°C.

2. The organic coated steel strip of claim 1 wherein said organic coating contains silica.

3. The organic coated steel strip of claim 1 wherein said organic coating has a thickness of 0.5 to 3 µm.

4. A method for making an organic coated steel strip having improved bake hardenability of 3.5 to 6.1 kgf/mm2, comprising the steps of:
depositing a layer of a zinc base alloy on one surface of an extra low carbon steel substrate containing 0.001 to 0.008 weight percent carbon and having bake hardenability in a weight of 10 to 40 g/m2, subjecting said substrate to a chromate treatment to form a chromate layer on the zinc base alloy layer in a weight of at least 10 mg/m2 calculated as metallic chromium, and applying an organic coating on the chromate layer and baking the coating at a temperature of up to 150°C.

5. The method of claim 4 wherein said chromate treatment uses an aqueous chromate solution containing a chromate compound, a reducing agent, and at least one member selected from acid residues, resins and silica.

6. A method for making an organic coated steel strip having improved bake hardenability of 3.5 to 6.1 kgf/mm2, comprising the steps of:
depositing a layer of a zinc base alloy on one surface of an extra low carbon steel substrate containing 0.001 to 0.008 weight percent carbon and having bake hardenability, subjecting said substrate to a chromate treatment to form a chromate layer on the zinc base alloy layer, and applying an organic coating on the chromate layer and baking the coating at a temperature of up to 150°C, wherein said chromate treatment uses an aqueous chromate solution containing a chromate compound, a reducing agent, and at least one member selected from acid residues, resins and silica.

7. The method of claim 6 wherein said reducing agent is selected from the group consisting of methanol, hydrogen peroxide, ethylene glycol, succinic acid, and succinimide.

8. The method of claim 7 wherein said reducing agent added is added in a sufficient amount of provide 0.2 to 1.9 gram atoms of hydrogen per gram molecule of CrO3.

9. The method of claim 6 wherein said acid residue is comprised of the residue of phosphoric or boric acid.

10. The method of claim 9 wherein said acid residue is added in an amount to give an acid residue to CrO3 ratio of from 0.05 to 0.3 by weight.

11. The method of claim 6 wherein said resin is comprised of an acrylic resin.

12. The method of claim 11 wherein said resin is added in an amount to give a resin to CrO3 ratio of from 0.1 to 20 by weight.

13. The method of claim 6 wherein said silica is comprised of colloidal silica.

14. The method of claim 13 wherein said silica is added in an amount to give a SiO2/CrO3 ratio of from 0.3 to 3.0 by weight.