COLD-ROLLED STEEL SHEET, METHOD OF MANUFACTURING COLD-ROLLED STEEL SHEET, AUTOMOBILE MEMBER AND FACILITY FOR MANUFACTURING COLD-ROLLED STEEL SHEET

A cold-rolled steel sheet has excellent chemical convertibility and excellent corrosion resistance after coating. A method of manufacturing a cold-rolled steel sheet includes first pickling applied to a steel sheet which is continuously annealed after cold rolling, second pickling applied to the steel sheet subsequently and, thereafter, neutralizing treatment applied to the steel sheet using an alkaline solution.

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Description
TECHNICAL FIELD

This disclosure relates to a cold-rolled steel sheet, and a method of manufacturing a cold-rolled steel sheet. The disclosure also relates to a facility for manufacturing the cold-rolled steel sheet. Particularly, the disclosure relates to a cold-rolled steel sheet having excellent chemical convertibility and, at the same time, corrosion resistance after coating which is evaluated by a hot brine dipping test and a composite cycle corrosion test, a method of manufacturing the cold-rolled steel sheet, and an automobile member. The cold-rolled steel sheet can be preferably used as a high-strength cold-rolled steel sheet containing Si and having a tensile strength TS of 590 MPa or more.

BACKGROUND

Recently, from a viewpoint of protecting a global environment, there has been a strong demand for improving fuel economy of automobiles. Further, from a viewpoint of securing safety of an occupant at the time of collision, there has been also a strong demand for the acquisition of high strength in a vehicle body of an automobile. To meet these demands, efforts have been positively made to impart high strength to a cold-rolled steel sheet which becomes a raw material for an automobile member and to reduce a thickness of the cold-rolled steel sheet thus achieving simultaneously the reduction in weight and the acquisition of a high strength in a vehicle body of an automobile. Also, many automobile members are manufactured by applying forming to a steel sheet and hence, the steel sheet which becomes a raw material in such forming is required to possess excellent formability in addition to a high strength.

There have been proposed various methods of increasing a strength of a cold-rolled steel sheet. As an effective means for acquiring high strength without largely impairing formability, a solid solution strengthening method with addition of Si is named. However, it is known that when a large amount of Si, particularly 0.5 mass % or more Si is added to a cold-rolled steel sheet, a large amount of Si containing oxide such as SiO2 or an Si—Mn based compound oxide is formed on an interface between a surface of the steel sheet and an oxide scale at the time of heating a slab, at the time of hot rolling or during annealing afterward. This Si containing oxide remarkably lowers chemical convertibility. Further, when the cold-rolled steel sheet is exposed to a severe corrosion environment such as a salt water spraying test or a composite cycle corrosion test where moistening and drying are repeated after electrodeposition coating, peeling of a coated film is liable to occur thus giving a rise to a drawback that a cold-rolled steel sheet exhibits inferior corrosion resistance after coating.

To cope with the drawback that the Si containing steel sheet has, for example, Japanese Unexamined Patent Application Publication No. 2004-204350 proposes a high strength cold-rolled steel sheet where a slab is heated at a temperature of 1200° c. or above at the time of hot rolling, descaling is performed at a high pressure, a surface of the hot-rolled steel sheet is ground by nylon brush containing abrasive grains before pickling, the sheet is dipped into a 9% hydrochloric acid tank twice to perform pickling to lower Si concentration on a surface of the steel sheet.

Japanese Unexamined Patent Application Publication No. 2004-244698 proposes a high strength cold-rolled steel sheet where corrosion resistance is enhanced by setting a line width of a filamentous oxide containing Si which is observed at a depth of 1 to 10 μm from a surface of the steel sheet to 300 nm or less.

Japanese Unexamined Patent Application Publication No. 64-62485 proposes a technique for enhancing an oxide removing ability of a steel sheet by setting an iron ion concentration (divalent) in a hydrochloric acid to 0.5 to 18%.

However, in the high strength cold-rolled steel sheet described in Japanese Unexamined Patent Application Publication No. 2004-204350, even when Si concentration in the surface of the steel sheet is lowered before cold rolling, an Si containing oxide is formed in the surface of the steel sheet by annealing performed after cold rolling and hence, the improvement of corrosion resistance after coating cannot be expected.

In the high strength cold-rolled steel sheet described in Japanese Unexamined Patent Application Publication No. 2004-244698, no problem arises with respect to corrosion resistance in a corrosion environment such as a salt water spraying test stipulated in JIS Z2371. However, the cold-rolled steel sheet cannot acquire sufficient corrosion resistance after coating in a severe corrosion environment such as a hot brine dipping test and a composite cycle corrosion test.

That is, with the mere lowering of Si concentration in a surface of a steel sheet after hot rolling or the mere reduction of an amount of filamentous oxide containing Si, a high strength cold-rolled steel sheet having excellent corrosion resistance after coating cannot be acquired.

In the technique described in Japanese Unexamined Patent Application Publication No. 64-62485, SiO2 is insoluble in a hydrochloric acid and hence, even when iron ion concentration is set to 0.5 to 18%, SiO2 cannot be removed.

In view of the above, as a technique which overcomes the above-mentioned drawbacks, Japanese Unexamined Patent Application Publication No. 2007-217743 discloses a technique which can enhance chemical convertibility by increasing reactivity of a steel sheet with a chemical conversion treatment solution by removing an Si containing oxide concentrated on a surface of the steel sheet in an annealing step or the like by pickling and by further imparting an S-based compound to such a surface.

Japanese Unexamined Patent Application Publication No. 2007-246951 discloses a technique where a P-based compound is imparted in place of an S-based compound described in Japanese Unexamined Patent Application Publication No. 2007-217743.

Japanese Unexamined Patent Application Publication No. 2012-132092 discloses, as a technique which can overcome the above-mentioned drawbacks, a technique which enhances chemical convertibility by increasing reactivity with chemical conversion treatment solution. In this technique, SiO2 is removed by performing pickling using an oxidizing acid in a first stage and a Fe-based oxide formed in the first-stage pickling is removed by performing pickling using a non-oxidizing acid in a subsequent second stage.

Recently, with the aim of lowering of industrial waste (suppression of generation of sludge) and the reduction in running cost, lowering of a temperature of chemical conversion treatment solution has been in progress. As a result, compared to a conventional chemical conversion treatment condition, reactivity of the steel sheet with a chemical conversion treatment solution with applied to a steel sheet has been largely lowered. Lowering of a temperature of a chemical conversion treatment solution does not cause any problem because of the improvement in a surface adjusting technique performed before chemical conversion treatment with respect to an ordinary steel sheet which has been conventionally used and contains a small amount of alloy. However, with respect to a high-strength cold-rolled steel sheet to which a large amount of Si is added, reactivity of the steel sheet with a chemical conversion treatment solution is remarkably lowered due to the influence of Si containing oxide formed on a surface layer of the steel sheet during an annealing step and hence, it is necessary to increase reactivity from a steel sheet side using any means. However, with the techniques disclosed in Japanese Unexamined Patent Application Publication No. 2007-217743 and Japanese Unexamined Patent Application Publication No. 2007-246951, even when a chemical conversion treatment solution is effective with respect to a conventional ordinary steel sheet, a sufficient improvement effect capable of coping with lowering of a temperature of a chemical conversion treatment solution cannot be expected with respect to a high-strength cold-rolled steel sheet containing a large amount of Si. On the other hand, it is known that with the use of the technique disclosed in Japanese Unexamined Patent Application Publication No. 2012-132092, the technique can cope with lowering of a temperature of a chemical conversion treatment solution even with respect to a high-strength cold-rolled steel sheet containing a large amount of Si. However, with the technique disclosed in Japanese Unexamined Patent Application Publication No. 2012-132092, when the concentration of Fe is low, a pickling speed is slow so that an ability of removing an Si containing oxide becomes insufficient, and when the concentration of Fe is high, an iron based oxide is formed so that chemical convertibility and eventually corrosion resistance after coating are also deteriorated. Further, with the technique disclosed in Japanese Unexamined Patent Application Publication No. 2012-132092, reactivity between a chemical conversion treatment solution and a surface of a steel sheet is high so that it is considered that a rate of occurrence of spot rust is increased during storage of a cold-rolled steel sheet for a long period.

It could therefore be helpful to provide a cold-rolled steel sheet which is excellent in not only chemical convertibility but also in corrosion resistance after coating, a method of manufacturing the cold-rolled steel sheet, and an automobile member as well as to provide a facility for manufacturing such a cold-rolled steel sheet.

SUMMARY

We carried out a detailed analysis of a steel sheet surface characteristic after annealing and extensive studies with respect to a method of increasing reactivity between a surface of a steel sheet and a chemical conversion treatment solution. As a result, we found that it is extremely important to apply strong pickling to a surface of a steel sheet which is continuously annealed after cold-rolling, to remove an Si containing oxide layer formed on a surface layer of the steel sheet during annealing, to reduce a steel sheet surface coverage of an iron-based oxide formed on the surface of the steel sheet by the above-mentioned strong pickling and to subsequently neutralize a residue of an acidic solution by an alkaline solution after strong pickling to enhance corrosion resistance after coating by preventing the occurrence of point rust during storage of a cold-rolled steel sheet.

We thus provide:

[1] A method of manufacturing a cold-rolled steel sheet where first pickling is applied to a steel sheet which is continuously annealed after cold rolling, second pickling is applied to the steel sheet subsequently and, thereafter, neutralizing treatment is applied to the steel sheet using an alkaline solution.
[2] The method of manufacturing a cold-rolled steel sheet described in [1] where the alkaline solution has pH of 9.5 or more, and one or two or more selected from a group consisting of sodium hydroxide, sodium carbonate, sodium hydrogen carbonate, orthophosphate and condensed phosphate are mixed into the alkaline solution.
[3] The method of manufacturing a cold-rolled steel sheet described in [1] or [2] where the neutralizing treatment is performed in a state that a temperature of the alkaline solution is set to a value which falls within a range of 20 to 70° C., and a treatment time is set to a value which falls within a range of 1 to 30 seconds.
[4] The method of manufacturing a cold-rolled steel sheet described in any one of [1] to [3] where the first pickling is performed using any one of a nitric acid, a hydrochloric acid, a hydrofluoric acid, a sulfuric acid and a mixture of two or more of these acids.
[5] The method of manufacturing a cold-rolled steel sheet described in any one of [1] to [4] where the first pickling is performed using either one of the following acidic solutions (a) and (b).
(a) The acidic solution containing a nitric acid and a hydrochloric acid, wherein concentration of nitric acid is more than 50 g/L and 200 g/L or less, a ratio R1 of the concentration of hydrochloric acid to the concentration of nitric acid (hydrochloric acid/nitric acid) is set to a value which falls within a range of 0.01 to 0.25, and the concentration of Fe ion is set to a value which falls within a range of 3 to 50 g/L.
(b) The acidic solution containing a nitric acid and hydrofluoric acid, wherein concentration of nitric acid is more than 50 g/L and 200 g/L or less, a ratio R2 of the concentration of hydrofluoric acid to the concentration of nitric acid (hydrofluoric acid/nitric acid) is set to a value which falls within a range of 0.01 to 0.25, and the concentration of Fe ion is set to a value which falls within a range of 3 to 50 g/L.
[6] The method of manufacturing a cold-rolled steel sheet described in any one of [1] to [5] where a non-oxidizing acid is used in the second pickling.
[7] The method of manufacturing a cold-rolled steel sheet described in [6] where the non-oxidizing acid is any one of a hydrochloric acid, a sulfuric acid, a phosphoric acid, a pyrophosphoric acid, a formic acid, an acetic acid, a citric acid, a hydrofluoric acid, an oxalic acid, and an acid which is a mixture of two or more of these acids.
[8] The method of manufacturing a cold-rolled steel sheet described in [6] or [7] where the non-oxidizing acid is any one of hydrochloric acid having the concentration of 0.1 to 50 g/L, a sulfuric acid having the concentration of 0.1 to 150 g/L and an acid which is a mixture of a hydrochloric acid having the concentration of 0.1 to 20 g/L and a sulfuric acid having the concentration of 0.1 to 60 g/L.
[9] The method of manufacturing a cold-rolled steel sheet described in any one of [1] to [8] where the second pickling is performed in a state that a temperature of the acidic solution is set to a value which falls within a range of 20° C. to 70° C., and a pickling time is set to a value which falls within a range of 1 to 30 seconds.
[10] The method of manufacturing a cold-rolled steel sheet described in any one of [1] to [9] where the steel sheet contains, as a component of the composition thereof, 0.5 to 3.0 mass % Si.
[11] The method of manufacturing a cold-rolled steel sheet described in [10] where the steel sheet further contains, as components of the composition thereof: 0.01 to 0.30 mass % C, 1.0 to 7.5 mass % Mn, 0.05 mass % or less P, 0.01 mass % or less S, 0.06 mass % or less Al, and Fe and unavoidable impurities as a balance.
[12] The method of manufacturing a cold-rolled steel sheet described in [11] where the steel sheet further contains, as components of the composition thereof, one or two or more of elements selected from a group consisting of 0.3 mass % or less Nb, 0.3 mass % or less Ti, 0.3 mass % or less V, 1.0 mass % or less Mo, 1.0 mass % or less Cr, 0.006 mass % or less B and 0.008 mass % or less N.
[13] The method of manufacturing a cold-rolled steel sheet described in [11] or [12] where the steel sheet further contains, as the components of the composition, one or two or more of elements selected from a group consisting of 2.0 mass % or less Ni, 2.0 mass % or less Cu, 0.1 mass % or less Ca, and 0.1 mass % or less REM.
[14] A cold-rolled steel sheet manufactured by the method of manufacturing a cold-rolled steel sheet described in any one of [1] to [13] where an Si containing oxide layer formed on a surface layer of the steel sheet is removed, and a surface coverage of an iron-based oxide existing on a surface of the steel sheet is 40% or less.
[15] The cold-rolled steel sheet described in [14] where a maximum thickness of the iron-based oxide existing on the surface of the steel sheet is 150 nm or less.
[16] An automobile member formed by using the cold-rolled steel sheet described in [14] or [15].
[17] A facility for manufacturing a cold-rolled steel sheet where a first pickling device, a second pickling device, an acid neutralizing treatment device, and a drying device are arranged in this order on a rear stage of a continuous annealing device.
[18] The facility for manufacturing a cold-rolled steel sheet described in [17] where a water cleaning device is arranged on a rear stage of the first pickling device, the second pickling device, and the acid neutralizing treatment device.
[19] The facility for manufacturing a cold-rolled steel sheet described in [17] or [18] where a water cleaning spray device is arranged on an inlet side and/or an outlet side of one or more devices selected from a group consisting of the first pickling device, the second pickling device, the acid neutralizing treatment device and the water cleaning device.

It is possible to obtain a cold-rolled steel sheet being excellent in chemical convertibility as well as corrosion resistance after coating. Further, according to the manufacturing method, a cold-rolled steel sheet having favorable chemical convertibility and favorable corrosion resistance after coating can be manufactured easily and in a stable manner through usual cold-rolling step and pickling step by merely adjusting a pickling condition.

It is possible to provide a cold-rolled steel sheet being excellent in chemical convertibility even when chemical conversion treatment solution having a low temperature is used and also being excellent in corrosion resistance after coating even in a severe corrosion environment such as a hot brine dipping test or a composite cycle corrosion test even when the cold-rolled steel sheet contains 0.5 to 3.0 mass % Si. In this manner, chemical convertibility and corrosion resistance after coating of a high strength cold-rolled steel sheet containing a large amount of Si thus having a tensile strength TS of 590 MPa or more can be largely improved and hence, the high strength cold-rolled steel sheet can be preferably used as a reinforcing member of a vehicle body of an automobile or the like.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A and 1B are views showing reflection electron images of surfaces of steel sheets which are cold-rolled steel sheet standard samples No. a and No. b prepared to obtain a surface coverage of an iron-based oxide.

FIG. 2 is a histogram of the number of pixels with respect to gray values of reflection electron image photographs of the cold-rolled steel sheet standard samples No. a and No. b.

FIG. 3 is a view showing a result of observation of a cross section of a steel sheet surface covering material after a surface of a steel sheet is pickled using a non-oxidizing acid by a transmission-type electron microscope.

FIG. 4 is a graph showing a result of an energy distribution type X-ray (EDX) analysis of an iron-based oxide observed in FIG. 3.

FIGS. 5A and 5B are graphs showing results obtained by measuring the distribution of O, Si, Mn and Fe in the depth direction on a surface of specimens shown in Table 2 by GDS.

 DETAILED DESCRIPTION

Details of our steel sheets and methods are described hereinafter. In the description made hereinafter, a unit of contents of the respective elements of the composition of steel is set to “mass %”, and “mass %” is expressed simply as “%” unless otherwise specified.

In an annealing step using a continuous annealing furnace which is performed to impart the desired structure, desired strength and desired formability to the cold-rolled steel sheet obtained through cold rolling by recrystallizing the cold-rolled steel sheet, a non-oxidizing gas or a reducing gas is usually used as an atmospheric gas, and a dew point is strictly controlled. Accordingly, in an ordinary general-use cold-rolled steel sheet having a low alloy content, oxidation of a surface of the steel sheet is suppressed. However, in a steel sheet containing 0.5% or more Si or Mn, even when the component or a dew point of an atmospheric gas is strictly controlled during annealing, Si, Mn or the like which is easily oxidized compared to Fe is oxidized so that the formation of an Si containing oxide such as an Si oxide (SiO2) or an Si—Mn based composite oxide on a surface of a steel sheet cannot be avoided. Although the structures of these oxides change depending on components of a steel sheet, an annealing atmosphere or the like, in general, the structures of these oxides often change depending on a mixture of components of a steel sheet and an annealing atmosphere. Further, it is known that the Si containing oxide is formed not only on a surface of a steel sheet but also in the inside of a base steel. Hence, an etching property of the surface of the steel sheet in chemical conversion treatment (zinc phosphate treatment) which is performed as a surface treatment for electrodeposition coating is impaired thus adversely affecting the formation of a sound chemical conversion treatment film.

On the other hand, recently, with the aim of reducing an amount of sludge generated at the time of chemical conversion treatment and a running cost, lowering of a temperature of a chemical conversion treatment solution has been in progress. As a result, compared to a conventional art, chemical conversion treatment can be performed in a state where reactivity of a chemical conversion treatment solution with a steel sheet is extremely low. Such a change in chemical conversion treatment condition does not cause any particular problem due to the improvement of a surface adjustment technique or the like with respect to an ordinary steel sheet which has been used conventionally and contains a small amount of alloy. However, with respect to a steel sheet which contains a large amount of alloy component, particularly with respect to a high strength cold rolled steel sheet which aims at a higher strength by containing a large amount of Si, the influence exerted by the above-mentioned change in chemical conversion treatment condition, that is, lowering of a temperature of a chemical conversion treatment solution is extremely large. To cope with this situation, with respect to a cold rolled steel sheet containing a large amount of Si, it is considered necessary to increase reactivity of the steel sheet with a chemical conversion treatment solution by activating a surface of the steel sheet per se corresponding to worsening of a chemical conversion treatment condition.

To cope with the above-mentioned worsening of the chemical conversion treatment condition, we studied a method of enhancing chemical convertibility of a steel sheet. As a result, we found that a method is effective where a surface of a cold-rolled steel sheet after continuous annealing is subjected to strong pickling using a nitric acid or the like as a pickling solution thus removing an Si containing oxide layer on a surface layer of the steel sheet formed by continuous annealing or the like after cold rolling. “Si containing oxide” means SiO2 or an Si—Mn based composite oxide formed along a surface of the steel sheet or a grain boundary in the inside of the steel sheet at heating of a slab, after hot rolling or at annealing after cold rolling. Although a thickness of a layer where the Si containing oxide is present changes depending on the composition of the steel sheet or an annealing condition (temperature, time, atmosphere), the thickness is usually approximately 1 μm from a surface of the steel sheet. Further, “removing an Si containing oxide layer” means that the Si containing oxide layer is removed by pickling to a level that a peak of Si and a peak of O do not appear when the surface of the steel sheet is analyzed in a depth direction by GDS (glow discharge atomic emission spectrochemical analysis).

The reason a strong acid such as a nitric acid is used as an above-mentioned pickling solution is that although an Si—Mn based composite oxide is easily dissolved by an acid among Si containing oxides, SiO2 exhibits insolubility and hence, to remove SiO2, it is necessary to remove an Si containing oxide formed on a surface of a steel sheet together with a base steel.

However, although chemical convertibility is largely improved by removing an Si containing oxide layer present on a surface of a steel sheet by performing strong pickling using a nitric acid or the like after continuous annealing, we found that there are some cases where a steel sheet exhibits inferior chemical convertibility. When we investigated the cause of the occurrence of such cases, we found that although an Si-based oxide layer is removed by the above-mentioned strong pickling using a nitric acid or the like, Fe which is dissolved from a surface of a steel sheet by pickling forms an iron-based oxide, and this iron-based oxide is deposited and precipitates on the surface of the steel sheet and covers the surface of the steel sheet thus lowering chemical convertibility, and when a residue of a pickling solution remains, a spot rust occurrence ratio during storage of a cold-rolled steel sheet is increased so that the cold-rolled steel sheet exhibits inferior corrosion resistance after coating.

We further found that, to reduce an adverse effect which affects chemical convertibility, it is important to suppress the formation of an iron-based oxide on a surface of a steel sheet to set a surface coverage of the iron-based oxide present on the surface of the steel sheet to 40% or less. We also found that an iron-based oxide present on the surface of the steel sheet can be dissolved and removed by performing pickling using a non-oxidizing acid after performing strong pickling. We also found that it is important to remove a residue of an acidic solution which remains after pickling performed two times by performing neutralizing treatment using an alkaline solution after performing pickling using a non-oxidizing acid.

Based on such findings, strong pickling is performed as first pickling to suppress the formation of an iron-based oxide on a surface of a steel sheet and to remove an Si containing oxide layer present on a surface of the steel sheet. Next, pickling is performed using a non-oxidizing acid as second pickling to set a surface coverage of the iron-based oxide present on the surface of the steel sheet to 40% or less. Subsequently, neutralizing treatment is applied to the steel sheet using an alkaline solution.

We also found that when a coverage of an iron-based oxide formed on a surface of a steel sheet by pickling is set to 40% or less and, further, a maximum thickness of the iron-based oxide is set to 150 nm or less, chemical convertibility is further improved and corrosion resistance is also improved and, as a means to achieve such effects, it is effective to properly set a pickling condition (concentration, temperature, time) and a non-oxidizing pickling condition (acid concentration, temperature, time).

“Iron-based oxide” means an oxide which contains iron as a main component where an atomic percentage of iron among elements other than oxygen which constitute oxides is set to 30% or more. The iron-based oxide is an oxide which is present on a surface of a steel sheet with a non-uniform thickness and differs from a natural oxide film having a uniform thickness of several nm and being present as a layer. Further, an iron-based oxide formed on a surface of a cold-rolled steel sheet is amorphous based on the observation using a transmission type electron microscope (TEM) or a result of analysis of a diffraction pattern obtained by an electron beam diffraction.

Next, our method of manufacturing a cold-rolled steel sheet is described.

First, pickling is applied to a steel sheet which is produced by applying heating, hot rolling, cold rolling and continuous annealing to a steel material (slab) containing 0.5 to 3.0% Si, for example, and second pickling is applied to the steel sheet subsequently and, thereafter, neutralizing treatment is applied to the steel sheet using an alkaline solution. By performing such pickling and neutralizing treatment, chemical convertibility and corrosion resistance after coating can be remarkably enhanced.

First Pickling Condition

After continuous annealing, a large amount of an Si containing oxide such as SiO2 or an Si—Mn based composite oxide is formed on a surface layer of a steel sheet. If this state is maintained as it is, chemical convertibility and corrosion resistance after coating are extremely lowered. In view of the above, according to the manufacturing method, it is preferable to apply, as the first pickling, strong pickling to a cold-rolled steel sheet after annealing using an acidic solution containing a nitric acid and a hydrochloric acid or an acidic solution containing a nitric acid and a hydrofluoric acid. By performing first pickling, an Si containing oxide layer formed on a surface of the steel sheet is removed together with a base steel.

Although an Si—Mn based composite oxide is easily dissolved by an acid among Si containing oxides, SiO2 exhibits insolubility against an acid. Accordingly, to remove an Si containing oxide including SiO2, it is necessary to remove an oxide layer together with a base steel of a steel sheet by strong pickling. Accordingly, as an acid which can be used as an acidic solution, a nitric acid which is a strong oxidizing acid can be favorably used. Further, provided that an acid can remove an Si containing oxide layer, the acid may be a hydrofluoric acid, a hydrochloric acid, a sulfuric acid or the like. That is, a kind of acid is not particularly specified. Further, an acid prepared by mixing these two or more of acids may be used. It is also effective to accelerate dissolving of a base steel by adding a pickling accelerating agent to an acidic solution or by using electrolytic treatment in combination with the use of an acid.

Further, as described previously, Fe which is dissolved from a surface of a steel sheet by pickling forms an iron-based oxide, and this iron-based oxide is deposited and precipitates on the surface of the steel sheet and covers the surface of the steel sheet thus giving rise to a possibility that chemical convertibility is lowered. To reduce a load of second pickling by avoiding such lowering of chemical convertibility, it is preferable to suppress an amount of iron-based oxide formed on a surface of a steel sheet. Due to the reasons described above, it is preferable to set the following pickling condition.

To remove an Si containing oxide efficiently, when an acidic solution containing a nitric acid and a hydrochloric acid is used, it is preferable that the acidic solution contain the nitric acid and the hydrochloric acid such that the concentration of nitric acid be set to a value which is more than 50 g/L to 200 g/L or less, and a ratio R1 (hydrochloric acid/nitric acid) of the concentration of hydrochloric acid having an oxide film breaking effect to the concentration of nitric acid be set to 0.01 to 0.25, and the concentration of Fe ion (sum of bivalence and trivalence) be set to 3 to 50 g/L. It is more preferable that the concentration of nitric acid be set to 100 g/L to 200 g/L. It is more preferable that the above-mentioned R1 be set to 0.02 to 0.15. It is more preferable that the concentration of Fe ion be set to 3 to 25 g/L. When an acidic solution containing a nitric acid and a hydrofluoric acid is used, it is preferable that the acidic solution contains the nitric acid and the hydrofluoric acid such that the concentration of nitric acid be set to more than 50 g/L to 200 g/L or less, and a ratio R2 (hydrofluoric acid/nitric acid) of the concentration of hydrofluoric acid having an oxide film breaking effect to the concentration of nitric acid be set to 0.01 to 0.25, and the concentration of Fe ion (sum of bivalence and trivalence) be set to 3 to 50 g/L. It is more preferable that the concentration of nitric acid be set to 100 g/L to 200 g/L. It is more preferable that the above-mentioned R2 be set to 0.02 to 0.15. It is more preferable that the concentration of Fe ion be set to 3 to 25 g/L. When R1 and R2 are larger than 0.25 or when the concentration of Fe ion (the sum of bivalence and trivalance) is less than 3 g/L, a desired pickling speed cannot be acquired and hence, an Si containing oxide cannot be efficiently removed. On the other hand, when R1 and R2 are smaller than 0.01 or when the concentration of Fe ion is larger than 50 g/L, although a desired pickling speed can be acquired, an amount of Fe ion in an acidic solution is large and hence, a large amount of Fe-based oxide is formed on a surface of the steel sheet whereby an Fe-based oxide cannot be completely removed by the second pickling. Accordingly, chemical convertibility and corrosion resistance cannot be improved.

Further, as a method of maintaining the concentration of Fe ion (the sum of bivalence and trivalence) at a value of 3 to 50 g/L, methods are considered including a method where when the concentration of Fe ion exceeds 50 g/L, an acidic solution is diluted, a method where a nitric acid or a hydrochloric acid is additionally charged, and a method where an iron component in an acid is lowered by an iron removing device.

Further, a maximum thickness of an iron-based oxide can be set to 150 nm or less by properly setting a pickling condition (concentration, temperature, time). By performing the first pickling in a state where a temperature of an acidic solution is set to 20 to 70° C. and a pickling time is 3 to 30 seconds, the maximum thickness of the iron based oxide becomes 150 nm or less and hence, chemical convertibility is further improved and the corrosion resistance is also further improved.

Second Pickling Condition

With mere strong pickling which is performed as the first pickling, it is difficult to control a surface coverage of an iron-based oxide formed on a surface of a steel sheet to 40% or less in a stable manner. In view of the above, to more surely reduce an amount of iron based oxide formed on a surface of a steel sheet by the above-mentioned first pickling, second pickling is performed. The second pickling is preferably performed using an acidic solution made of a non-oxidizing acid, and an iron-based oxide is removed by dissolving by second pickling.

As a non-oxidizing acid, one kind or two or more kinds selected from a group consisting of a hydrochloric acid, a sulfuric acid, a phosphoric acid, a pyrophosphoric acid, a formic acid, an acetic acid, a citric acid, a hydrofluoric acid, and an oxalic acid are preferably used. Although any acid may be used, a hydrochloric acid and a sulfuric acid which are used commonly in a steel making industry may be preferably used. Among these acids, a hydrochloric acid can be preferably used since a hydrochloric acid is a volatile acid so that a residue such as a sulfate group minimally remains on a surface of a steel sheet after water cleaning unlike a sulfuric acid, and an oxide breaking effect by chloride ion is large and the like. Further, a mixed acid prepared by mixing a hydrochloride acid and a sulfuric acid may be used.

Among these acids, from a viewpoint of preventing an insufficient removal of an iron-based oxide and the degradation of a surface property of a steel sheet due to an excessive pickling, it is preferable to use any one of a hydrochloric acid having the concentration of 0.1 to 50 g/L, a sulfuric acid having the concentration of 0.1 to 150 g/L, and a mixed acid prepared by mixing a hydrochloric acid having the concentration of 0.1 to 20 g/L and a sulfuric acid having the concentration of 0.1 to 60 g/L.

It is preferable that the second pickling be performed in a state where a temperature of an acidic solution is set to 20 to 70° C. and a pickling time is 1 to 30 seconds. When a temperature of an acidic solution is set to 20° C. or above and a treatment time is 1 second or more, it is sufficient to remove an iron-based oxide remaining on a surface of a steel sheet. On the other hand, when the temperature of an acidic solution is set to 70° C. or below and a treatment time is 30 seconds or less, a surface of a steel sheet is not excessively dissolved so that there is no possibility that a new surface oxide film will be formed. It is more preferable to set a temperature of an acidic solution of 30 to 50° C. Further, it is more preferable to set a pickling time to 2 to 20 seconds.

Further, to acquire a steel sheet which is more excellent in chemical convertibility and corrosion resistance, it is preferable to surely decrease a maximum thickness of an iron-based oxide present on a surface of a steel sheet after the above-mentioned pickling to 150 nm or less. To this end, it is preferable to properly increase the concentration of an acidic solution consisting of a non-oxidizing acid. For example, when a hydrochloric acid is used, the concentration of hydrochloric acid is preferably set to 3 to 50 g/L. When a sulfuric acid is used, the concentration of sulfuric acid is preferably set to 8 to 150 g/L. Further, when a pickling solution prepared by mixing a hydrochloric acid and a sulfuric acid is used, it is preferable to use an acid prepared by mixing a hydrochloric acid having the concentration of 3 to 20 g/L and a sulfuric acid having the concentration of 8 to 60 g/L. Provided that the concentration of a pickling solution falls within the above-mentioned concentration range, a thickness of an iron-based oxide can be surely decreased to 150 nm or below and, hence, chemical convertibility and corrosion resistance after coating can be enhanced. Further, provided that the concentration of a pickling solution falls within the above-mentioned concentration range, a surface of a steel sheet is not excessively resolved so that there is no possibility that a new surface oxide film is formed.

Neutralizing Treatment Condition

Our method is characterized in that neutralizing treatment is further performed using an alkaline solution after second pickling is performed.

When reactivity of a surface of a steel sheet is increased by removing an oxide formed during annealing by pickling, a residue of a pickling solution remains and hence, there is a possibility that point rust occurs during storage of a cold-rolled steel sheet. To suppress the occurrence of such spot rust, in the neutralizing treatment performed after pickling and re-pickling, it is preferable to perform neutralizing treatment using an alkaline solution having pH of 9.5 or more in which one kind or two or more kinds selected from a group consisting of sodium hydroxide, sodium carbonate, sodium hydrogen carbonate, orthophosphate and condensed phosphate are mixed. Such an alkaline solution is used to remove a residue of the pickling solution by neutralization. Also, when pH is less than 9.5, a residue of a pickling solution cannot be completely neutralized. As the condensed phosphate, for example, sodium pyrophosphate, sodium polyphosphate and the like are named. The above-mentioned pH is more preferably set to 10.0 to 12.0.

In performing neutralizing treatment using the above-mentioned alkaline solution, it is preferable that a temperature of the alkaline solution be set to 20 to 70° C., and a treatment time be set to 1 to 30 seconds. When a solution temperature of the alkaline solution is set to 20° C. or above and the treatment time is set to 1 second or more, a residue of a pickling solution is sufficiently neutralized. On the other hand, when a temperature of a pickling solution exceeds 70° C., an alkaline fume is generated. Further, when a treatment time exceeds 30 seconds, a length of a facility is elongated so that a huge facility cost becomes necessary. A temperature of the alkaline solution is more preferably set to 30 to 50° C. It is more preferable to set a treatment time of 2 to 20 seconds.

As described above, after continuous annealing, a steel sheet is subjected to first pickling and second pickling and, then, the steel sheet is subjected to neutralizing treatment using an alkaline solution. Thereafter, the steel sheet is formed into a product sheet (cold-rolled steel sheet) through usual treatment steps such as temper rolling.

A pickling method, that is, a method of bringing a steel sheet into contact with an acidic solution is not particularly limited. As such a method, a method in which an acidic solution is sprayed to a steel sheet, a method in which a steel sheet is dipped into an acidic solution and the like are named.

Further, it is preferable that first pickling and second pickling are continuously performed. By performing the first pickling and the second pickling continuously, it is possible to prevent natural oxidation of a steel sheet after the first pickling and hence, the steel sheet can be formed into a final product at a stroke whereby the product can be manufactured at a low cost.

Also, water cleaning treatment may be performed after first pickling, after second pickling and after neutralizing treatment respectively. Further, in performing first pickling, second pickling, neutralizing treatment and water cleaning treatment respectively, additional water cleaning may be further performed on an inlet side and/or on an outlet side of the respective treatments using a water cleaning spray. It is preferable that drying treatment is performed using a dryer or the like after water cleaning treatment.

Next, the composition of the cold-rolled steel sheet is described.

It is preferable that the steel sheet has the composition which allows the steel sheet to have a high strength such that the steel sheet can be used for forming a suspension member of an automobile and also has favorable chemical convertibility.

In the composition of the cold-rolled steel sheet, the content of Si is preferably set to 0.5 to 3.0%. Si is an element highly effective in increasing strength of steel (solid solution strengthening ability) without largely deteriorating workability of steel and hence, Si is an effective element in achieving high strengthening of steel. However, Si is also an element which adversely affects chemical convertibility and corrosion resistance after coating. Due to such reasons, while it is preferable to add 0.5% or more of Si, when the content of Si exceeds 3.0%, hot rolling property and cold rolling property are largely lowered thus giving rise to a possibility that productivity is adversely affected or ductility of a steel sheet per se is lowered. Accordingly, when Si is added as a component of the composition, the content of Si is preferably set to 0.5 to 3.0%. The content of Si is more preferably set to 0.8 to 2.5%.

It is permissible that the cold-rolled steel sheet contains components other than the above-mentioned components within the component range of the ordinary cold-rolled steel sheet. However, in applying the cold-rolled steel sheet to a high strength cold-rolled steel sheet having a tensile strength TS of 590 MPa or more which is used to form a vehicle body of an automobile or the like, it is preferable to set the contents of desired components other than the above-mentioned components as follows.

C: 0.01 to 0.30%

C is an element effective in increasing strength of steel. C is also an element effective in forming residual austenite having TRIP (Transformation Induced Plasticity) effect, bainite or martensite. When the content of C is set to 0.01% or more, the above-mentioned effects can be obtained. On the other hand, when the content of C is 0.30% or less, lowering of weldability does not occur. Accordingly, the content of C to be added is preferably set to 0.01 to 0.30%, and the content of C is more preferably set to 0.10 to 0.20%.

Mn: 1.0 to 7.5%

Mn is an element having a function of increasing strength of steel by solid solution strengthening of steel, a function of enhancing hardenability and a function of accelerating formation of residual austenite, bainite or martensite. Such an effect can be realized by adding 1.0% or more Mn. On the other hand, when the content of Mn is 7.5% or less, the above-mentioned advantageous effect can be obtained without the increase of cost. Accordingly, the content of Mn to be added is preferably set to 1.0 to 7.5%, and the content of Mn is more preferably set to 2.0 to 5.0%.

P: 0.05% or Less

P is an element which does not deteriorate a drawability although P has a large solid solution strengthening ability and is also an element effective for acquiring a high strength. Accordingly, the content of P is preferably set to 0.005% or more. Although P is an element which deteriorates a spot weldability, there arises no problem provided that the content of P is set to 0.05% or less. Accordingly, the content of P is preferably set to 0.05% or less, and the content of P is more preferably set to 0.02% or less.

S: 0.01% or Less

S is an impurity element which is unavoidably mixed into steel. S is a harmful component which precipitates as MnS in steel and lowers the stretch-flangeability of the steel sheet. To prevent the stretch-flangeability from being lowered, the content of S is preferably set to 0.01% or less. The content of S is more preferably set to 0.005% or less, and the content of S is still further preferably set to 0.003% or less.

Al: 0.06% or Less

Al is an element to be added as a deoxidizing agent in a steel making step. Further, Al is an element effective in separating non-metallic inclusion which lowers the stretch-flangeability as a slag. Accordingly, the content of Al is preferably set to 0.01% or more. When the content of Al is 0.06% or less, the above-mentioned effects can be obtained without increasing a cost of raw material. Accordingly, the content of Al is preferably set to 0.06% or less. The content of Al is more preferably set to 0.02 to 0.06%.

The cold-rolled steel sheet may contain one or two or more of elements selected from a group consisting of 0.3% or less Nb, 0.3% or less Ti, 0.3% or less V, 1.0% or less Mo, 1.0% or less Cr, 0.006% or less B and 0.008% or less N in addition to the above-mentioned components.

Nb, Ti and V are elements which form carbide and nitride, make the microstructure fine by suppressing the growth of ferrite in a heating step during annealing, and enhance formability, particularly the stretch-flangeability. Further, Mo, Cr and B are elements which enhance hardenability of steel and accelerate formation of bainite or martensite. Accordingly, Nb, Ti, V, Mo, Cr, and B may be added to the steel within the above-mentioned ranges. Further, N is an element which forms nitride with Nb, Ti and V or is dissolved in steel in a solid solution state and hence, N contributes to increasing of strength of steel. When the content of N is set to 0.008 mass % or less, a large amount of nitride is not formed and hence, breakage due to the formation of void at press forming is suppressed whereby the above-mentioned effects can be obtained.

The cold-rolled steel sheet may also contain one or two or more selected from a group consisting of 2.0% or less Ni, 2.0% or less Cu, 0.1% or less Ca and 0.1% or less REM in addition to the above-mentioned composition of components.

Ni and Cu are elements effective in accelerating formation of a low temperature transformation phase and increasing a strength of steel. Accordingly, Ni and Cu which fall within the above-mentioned ranges may be added to the steel sheet. Also, Ca and REM are elements which control a morphology of sulfide-based inclusion and enhance the stretch-flangeability of the steel sheet. Accordingly, Ca and REM which fall within the above-mentioned ranges may be added to the steel sheet.

In the cold-rolled steel sheet, a balance other than the above-mentioned components is Fe and unavoidable impurities. However, the cold-rolled steel sheet may contain other components unless such components impair the desired effects.

Next, a surface characteristic of a cold-rolled steel sheet is described. As described previously, a cold-rolled steel sheet has a steel sheet surface from which an Si containing oxide layer such as SiO2 and an Si—Mn based composite oxide formed on a surface layer of the steel sheet during annealing is removed. To acquire such a cold-rolled steel sheet, it is necessary to perform neutralizing treatment using an alkaline solution after the first pickling and the second pickling.

Further, in acquiring the cold-rolled steel sheet, it is necessary to decrease a surface coverage of an iron-based oxide present on a surface of a steel sheet to 40% or less besides the removal of the Si containing oxide layer. This is because when the surface coverage exceeds 40%, an iron dissolving reaction generated by chemical conversion treatment is obstructed so that a growth of chemical conversion crystals such as zinc phosphate or the like is suppressed. However, when a chemical conversion treatment solution having a low temperature is used, particularly with respect to a cold-rolled steel sheet used in an application where extremely severe corrosion resistance after coating is required as in the case of a suspension member of a vehicle which is exposed to severe corrosion, a coverage of 40% or less is insufficient, and it is necessary to further decrease the coverage to 35% or less. It is preferable to set the coverage to 35% or less.

The above-mentioned surface coverage of an iron-based oxide is obtained as follows. A surface of a steel sheet after pickling is observed using a scanning electron microscope (ULV-SEM) of an extremely low acceleration voltage which can detect extreme surface layer information at approximately five fields of view with an acceleration voltage of 2 kV, a working distance of 3.0 mm and a magnification of approximately 1000 times, and a spectroscopic analysis is performed using an energy dispersion type X-ray spectrometer (EDX) thus obtaining a reflection electron image. A binary coded processing is applied to the reflected electron image using an image analysis software, for example, Image J thus measuring an area ratio of a black-colored portion, and a surface coverage of an iron-based oxide can be obtained by averaging measured values of the respective fields of view. In addition, as the above-mentioned scanning electron microscope (ULV-SEM) of an extremely low acceleration voltage, for example, ULTRA55 made by SEISS Inc. may be named. Further, as the energy dispersion type X-ray spectrometer (EDX), for example, NSS312E made by Thermo Fisher Inc. may be named.

A threshold value used in the above-mentioned binary coded processing is described. A steel slab having a steel symbol G shown in Table 3 of an example described later was subjected to hot rolling, cold rolling and continuous annealing under a condition indicated at No. 93 of Table 4 in the example described later in the same manner so that the steel slab was formed into a cold-rolled steel sheet having a sheet thickness of 1.8 mm. Next, the cold-rolled steel sheet after continuous annealing was subjected to pickling, water cleaning and drying under a condition shown in Table 1 and, thereafter, the cold-rolled steel sheet was subjected to temper rolling with elongation of 0.7% thus manufacturing two kinds of cold-rolled steel sheets No. a and No. b which differ from each other in an amount of an iron-based oxide on a surface of the steel sheet. Then, while using the cold-rolled steel sheet No. a as a standard sample having a large amount of iron-based oxide and the cold-rolled steel sheet No. b as a standard sample having a small amount of iron-based oxide, a reflection electron image was obtained with respect to the respective steel sheets under the above-mentioned conditions using a scanning electron microscope. FIGS. 1A and 1B show reflection electron image photographs of the steel sheets No. a and No. b, and FIG. 2 shows a histogram of the number of pixels with respect to gray values of the reflection electron image photographs of the steel sheets No. a and No. b. A gray value (Y point) corresponding to an intersection (X point) of the histograms of No. a and No. b shown in FIG. 2 was set as a threshold value. When surface coverage of an iron-based oxide was obtained with respect to the steel sheets No. a and No. b using the above-mentioned threshold value, the surface coverage of the steel sheet No. a was 85.3% and the surface coverage of the steel sheet No. b was 25.8%.

TABLE 1 First pickling condition Second pickling condition Acid Treatment Acid Treatment Surface coverage Steel concentration Temperature time concentration Temperature time of iron-based sheet (g/l) (° C.) (sec.) (g/l) (° C.) (sec.) oxide (%) a nitric acid: 250 + 40 10 — — — 85.3 hydrochloric acid: 25 b nitric acid: 150 + 40 10 hydrochloric 40 30 25.8 hydrochloric acid: 15 acid: 10

To further enhance chemical convertibility and eventually corrosion resistance after coating, it is preferable that, in addition to the condition that a surface coverage of an iron oxide on a surface of a steel sheet after second pickling is 40% or below, a maximum thickness of the iron-based oxide be 150 nm or less. This is because when the maximum thickness of the iron-based oxide is 150 nm or less, there is no possibility that a dissolving reaction of iron by chemical conversion treatment is locally impaired, so that the precipitation of chemically converted crystals such as zinc phosphate cannot be locally suppressed. The maximum thickness of an iron-based oxide may preferably set to 130 nm or less.

The maximum thickness of an iron-based oxide is obtained as follows.

First, 10 pieces of extraction replicas by which a cross section of a steel sheet having a length of approximately 8 μm with respect to a width direction of the steel sheet can be observed were prepared by focused ion beam (FIB) working from a surface of the steel sheet after pickling. Next, using a transmission electron microscope (TEM) equipped with an energy dispersion type X-ray spectrometer (EDX) capable of investigating local information of the cross section, the cross sections of 8 μm of the respective replicas were continuously photographed with an acceleration voltage of 200 kV and at a magnification of 100,000. As one example, FIG. 3 shows a photograph obtained by observing a cross section of a coating layer formed by first pickling present on a surface of a steel sheet by a transmission electron microscope (TEM), and FIG. 4 shows a result of an EDX analysis of the coating layer. It is understood from FIG. 4 that the coating layer is formed of an iron-based oxide and hence, a distance between a line A indicating a base steel of the steel sheet and a line B indicating the most largest portion of the iron-based oxide layer shown in the photograph of the cross section in FIG. 3 was measured with respect to all of ten replicas, and the maximum thickness among the measured maximum thicknesses is assumed as the maximum thickness of the iron-based oxide. Further, it is needless to say that the sizes and the number of the above-mentioned replicas, measurement conditions by the TEM and the like are provided as only one example, and may be changed as desired.

The cold-rolled steel sheet obtained by the above-mentioned method exhibits excellent chemical convertibility and also exhibits excellent corrosion resistance after coating which is evaluated by a hot brine dipping test and a composite cycle corrosion test and, hence, the cold-rolled steel sheet can be preferably used to produce automobile members.

Example 1

Our steel sheets and methods are described in more detail by reference to examples.

Steel having the composition containing 0.125% C, 1.5% Si, 2.6% Mn, 0.019% P, 0.008% S and 0.040% Al and comprising Fe and unavoidable impurities as a balance was manufactured such that molten steel was produced by an ordinary refining process including a converter treatment, a degassing treatment and the like and molten steel was formed into steel materials (slabs) by continuous casting. Next, the slabs were reheated to a temperature of 1150 to 1170° C. and, thereafter, were subjected to hot rolling where a finish rolling completion temperature is set to 850 to 880° C., and were wound up into coils at a temperature of 500 to 550° C. thus forming hot-rolled steel sheets having a thickness of 3 to 4 mm. Next, scales were removed from the steel sheets by applying pickling to these hot-rolled steel sheets and, thereafter, cold rolling was applied to the steel sheets thus obtaining cold-rolled steel sheets having a thickness of 1.8 mm. Next, continuous annealing was performed where these cold-rolled steel sheets were heated to a soaking temperature of 750 to 780° C. and were held for 40 to 50 seconds and, thereafter, these steel sheets were cooled to a cooling stop temperature of 350 to 400° C. from the soaking temperature at a cooling rate of 20 to 30° C./second and were held for 100 to 120 seconds at a cooling stop temperature range. Thereafter, pickling, water cleaning and drying were applied to surfaces of the steel sheets under conditions shown in Table 2-1 to Table 2-2 (hereinafter, Table 2-1 and Table 2-2 being also collectively referred to as Table 2). Thereafter, temper rolling was applied to the steel sheets at a rate of elongation of 0.7% thus obtaining cold-rolled steel sheets No. 1 to No. 82 shown in Table 2.

Specimens were sampled from the above-mentioned respective cold-rolled steel sheets. Surfaces of the steel sheets were observed using a scanning electron microscope (ULV-SEM; made by SEISS Inc.; ULTRA55) at an extremely low acceleration voltage at five fields of view with an acceleration voltage of 2 kV, a working distance of 3.0 mm and a magnification of 1000 times, and spectroscopic analysis was performed using an energy dispersion type X-ray spectrometer (EDX; made by Thermo Fisher Inc.; NSS312E) thus obtaining reflected electron images. A binary coded processing was applied to the reflected electron images using an image analysis software (Image J) while setting gray values (Y points) corresponding to intersection points (X points) of histogram of the above-mentioned standard samples No. a and No. b as threshold values thus measuring area ratios of black-colored portions, and an average value of the area ratios at five fields of view was obtained and the average value was set as a surface coverage of an iron-based oxide.

Further, specimens were sampled from the above-mentioned respective cold-rolled steel sheets, and spot rust generation evaluation of the cold-rolled steel sheets was carried out under the following conditions. After a chemical conversion treatment and a coating treatment were applied to the specimens under the following conditions, specimens were subjected to three kinds of corrosion tests consisting of a hot brine dipping test, a salt water spraying test and a composite cycle corrosion test and, then, the corrosion resistance after coating was evaluated. Further, the distribution of O, Si, Mn and Fe in the depth direction on surfaces of the specimens sampled from the respective cold-rolled steel sheets was measured using a GDS.

(1) Spot Rust Generation Evaluation During Storage of Cold-Rolled Steel Sheets

After anti-rust oil was applied to the above-mentioned respective cold-rolled steel sheets, the cold-rolled steel sheets were left outdoors while preventing influences from external factors such as dusts. Presence or non-presence of generation of spot rust on the cold-rolled steel sheets was checked after approximately one month elapsed from starting the test. The evaluation “0” is given to cases where the specimens had no spot rust, and the evaluation “X” is given to cases where the specimens had spot rust.

(2) Chemical Conversion Treatment Condition

A chemical conversion treatment was applied to specimens sampled from the above-mentioned respective cold-rolled steel sheets using a degreasing agent: FC-E2011, a surface conditioner: PL-X and a chemical conversion treatment agent: palbond PB-L3065 made by Nihon Parkerizing Co., Ltd. such that a coating weight of chemical conversion treatment coating was set to 1.7 to 3.0 g/m2 under two conditions, that is, the standard condition and the comparison condition under a low temperature by lowering a temperature of a chemical conversion treatment solution.

Standard Condition

Degreasing step: treatment temperature 40° C., treatment time 120 seconds Spray degreasing and surface adjustment steps: pH 9.5, treatment temperature room temperature, treatment time 20 seconds
Chemical conversion treatment step: temperature of chemical conversion treatment solution 35° C., treatment time 120 seconds

Temperature Lowering Condition

Condition where a temperature of chemical conversion treatment solution in the above-mentioned standard condition was lowered to 33° C.

(3) Corrosion Test

Electrodeposition coating was applied to surfaces of the specimens to which the above-mentioned chemical conversion treatment had been applied by electrodeposition paint: V-50 made by NIPPONPAINT Co., Ltd. such that a film thickness of electrodeposition coating is set to 25 μm, and the specimens were subjected to the following three kinds of corrosion tests. Hot brine dipping test

A crosscut flaw having a length of 45 mm is formed by a cutter on a surface of the above-mentioned specimen (n=1, “n=1” meaning that the number of specimens is 1) to which chemical conversion treatment and electrodeposition coating were applied and thereafter, the specimen was dipped into 5 mass % NaCl aqueous solution (60° C.) for 360 hours. Then, the specimen was cleaned with water, was dried, and an adhesive tape was adhered to the cut flaw portion. Thereafter, a tape peeling test in which the adhesive tape is peeled was performed, and a maximum total width of peeling including left and right sides of the cut flaw portion was measured. When the maximum peeling total width is 6.0 mm or less, it is determined that the specimen is not defective. When the maximum total width of peeling is 5.0 mm or less, it can be evaluated that corrosion resistance of the specimen in the hot brine dipping test is favorable. Salt water spraying test (SST)

A crosscut flaw having a length of 45 mm is formed by a cutter on a surface of the above-mentioned specimen (n=1) to which chemical conversion treatment and electrodeposition coating were applied and, thereafter, the specimen was subjected to a salt water spraying test for 1200 hours in accordance with a neutral salt water spraying test stipulated in JIS Z2371:2000 using 5 mass % NaCl aqueous solution. Thereafter, a tape peeling test was carried out with respect to the crosscut flaw portion, and a maximum total width of peeling including left and right sides of the cut flaw portion was measured. When the maximum total width of peeling is 5.2 mm or less, it is determined that the specimen is not defective. When the maximum total width of peeling is 4.0 mm or less, it can be evaluated that corrosion resistance of the specimen in the salt water spraying test is favorable.

Composite Cycle Corrosion Test (CCT)

A crosscut flaw having a length of 45 mm is formed by a cutter on a surface of the above-mentioned specimen (n=1) to which chemical conversion treatment and electrodeposition coating were applied and, thereafter, the specimen was subjected to a corrosion test where one cycle formed of salt water spraying (5 mass % NaCl aqueous solution: 35° C., relative humidity: 98%)×2 hours→drying (60° C., relative humidity: 30%)×2 hours→wetting (50° C., relative humidity: 95%)×2 hours was repeated 120 times, was cleaned with water and, thereafter, was dried. Then, a tape peeling test was carried out with respect to the cut flaw portion, and a maximum total width of peeling including left and right sides of the cut flaw portion was measured. When the maximum total width of peeling is 7.8 mm or less, it is determined that the specimen is not defective. When the maximum total width of peeling is 6.0 mm or less, it can be evaluated that the corrosion resistance of the specimen in the composite cycle corrosion test is favorable.

The result of the above-mentioned test is shown in Table 2 together with the condition for the test.

TABLE 2 First pickling condition Fe ion Second pickling condition Neutralization condition Acid concen- Temper- Treatment Acid Temper- Treatment Temper- Treatment concentration tration ature time concentration ature time ature time No (g/l) (g/l) (° C.) (sec.) (g/l) (° C.) (sec.) Alkali pH (° C.) (sec.) 1 nitric acid: 150 + 5.5 40 10 — — — — — — 2 hydrochloric acid: 15 hydrochloric acid: 0.1 40 1 sodium 30 20 3 10 polyphosphate 30 20 4 30 pH 9.7 30 20 5 hydrochloric acid: 10 20 1 trisodium 40 10 6 10 phosphate 40 10 7 30 pH 11.5 40 10 8 hydrochloric acid: 10 40 1 sodium 50 5 pyrophosphate pH 11.0 9 10 — — — 10 30 sodium 50 5 pyrophosphate pH 11.0 11 hydrochloric acid: 10 70 1 sodium 40 5 12 10 hydroxide 40 5 13 30 pH 12.1 40 5 14 hydrochloric acid: 50 40 1 sodium 50 20 15 10 carbonate 50 20 16 30 pH 10.3 50 20 17 hydrochloric acid: 100 40 1 sodium 60 30 18 10 hydrogen 60 30 19 30 carbonate 60 30 pH 9.6 20 nitric acid: 50 + 7.3 40 10 hydrochloric acid: 0.1 40 1 sodium 30 20 21 hydrofluoric acid: 50 10 polyphosphate 30 20 22 30 pH 9.7 30 20 23 hydrochloric acid: 10 20 1 trisodium 40 10 24 10 phosphate 40 10 25 30 pH 11.5 40 10 26 hydrochloric acid: 10 40 1 sodium 50 5 27 10 pyrophosphate 50 5 28 30 pH 11.0 50 5 29 hydrochloric acid: 10 70 1 sodium 40 5 30 10 hydroxide 40 5 31 30 pH 12.1 40 5 32 hydrochloric acid: 50 40 1 sodium 50 20 33 10 carbonate 50 20 34 30 pH 10.3 50 20 35 hydrochloric acid: 100 40 1 sodium 60 30 36 10 hydrogen 60 30 37 30 carbonate 60 30 pH 9.6 Total width of peeling after corrosion test (mm) Surface characteristic Temperature of chemical conversion treatment solution Surface coverage of Generation of spot rust 35° C. 33° C. iron-based oxide not present: ∘ Hot brine Salt water Compound cycle No (%) present: x dipping test spraying test corrosion test Remarks 1 72.6 x 6.3 5.5 7.9 8.3 comparison example 2 39.4 ∘ 4.9 3.9 5.7 5.9 our example 3 35.1 ∘ 4.7 3.9 5.6 5.7 our example 4 30.2 ∘ 4.5 3.6 5.1 5.2 our example 5 39.2 ∘ 4.8 4.0 5.9 5.6 our example 6 35.9 ∘ 4.8 3.8 5.3 5.4 our example 7 31.1 ∘ 4.7 3.7 5.2 5.2 our example 8 35.4 ∘ 4.6 3.7 5.2 5.5 our example 9 30.3 x 4.5 3.6 4.8 5.0 comparison example 10 25.7 ∘ 4.1 3.3 4.5 4.6 our example 11 31.1 ∘ 4.3 3.5 4.7 5.0 our example 12 25.2 ∘ 4.2 3.1 4.2 4.9 our example 13 22.4 ∘ 3.8 3.0 4.1 4.3 our example 14 30.0 ∘ 4.2 3.2 4.7 4.7 our example 15 25.9 ∘ 4.1 3.1 4.4 4.6 our example 16 21.3 ∘ 3.6 3.0 3.9 4.2 our example 17 49.9 ∘ 5.4 4.3 6.6 6.6 our example 18 54.7 ∘ 5.7 4.8 7.1 7.3 our example 19 59.9 ∘ 5.9 5.2 7.4 7.5 our example 20 39.6 ∘ 4.8 3.9 5.8 5.9 our example 21 35.9 ∘ 4.7 3.7 5.3 5.5 our example 22 32.1 ∘ 4.1 3.6 5.2 5.1 our example 23 39.4 ∘ 4.9 3.9 5.5 5.6 our example 24 36.9 ∘ 4.8 3.9 5.6 5.7 our example 25 33.5 ∘ 4.6 3.5 5.4 5.2 our example 26 35.9 ∘ 4.7 3.8 5.4 5.9 our example 27 32.3 ∘ 4.5 3.6 5.2 5.4 our example 28 28.4 ∘ 4.3 3.6 4.9 4.9 our example 29 31.9 ∘ 4.5 3.6 5.1 5.4 our example 30 26.9 ∘ 4.2 3.1 4.6 4.8 our example 31 24.0 ∘ 3.9 3.2 4.3 4.5 our example 32 31.1 ∘ 4.2 3.4 4.5 5.2 our example 33 25.5 ∘ 4.1 3.3 4.2 4.8 our example 34 22.1 ∘ 3.8 3.2 3.8 4.1 our example 35 45.8 ∘ 5.2 4.1 6.1 6.3 our example 36 55.2 ∘ 5.7 4.8 7.1 7.3 our example 37 62.0 ∘ 6.0 5.1 7.2 7.8 our example First pickling condition Fe ion Second pickling condition Neutralization condition Acid concen- Temper- Treatment Acid Temper- Treatment Temper- Treatment concentration tration ature time concentration ature time ature time No (g/l) (g/l) (° C.) (sec.) (g/l) (° C.) (sec.) Alkali pH (° C.) (sec.) 38 nitric acid: 150 + 4.9 40 10 sulfuric acid: 0.1 40 1 sodium 30 20 39 hydrochloric 10 polyphosphate 30 20 40 acid: 15 30 pH 9.7 30 20 41 sulfuric acid: 75 20 1 trisodium 40 10 42 10 phosphate 40 10 43 30 pH 11.5 40 10 44 sulfuric acid: 75 40 1 sodium 50 5 45 10 pyrophosphate 50 5 46 30 pH 11.0 50 5 47 sulfuric acid: 75 70 1 sodium 40 5 48 10 hydroxide 40 5 49 30 pH 12.1 40 5 50 sulfuric acid: 150 40 1 sodium 50 20 51 10 carbonate 50 20 52 30 pH 10.3 50 20 53 sulfuric acid: 200 40 1 sodium 60 30 54 10 hydrogen 60 30 55 30 carbonate 60 30 pH 9.6 56 nitric acid: 50 + 8.1 40 10 sulfuric acid: 0.1 40 1 sodium 30 20 57 hydrofluoric 10 polyphosphate 30 20 58 acid: 50 30 pH 9.7 30 20 59 sulfuric acid: 75 20 1 trisodium 40 10 60 10 phosphate 40 10 61 30 pH 11.5 40 10 62 sulfuric acid: 75 40 1 sodium 50 5 63 10 pyrophosphate 50 5 64 30 pH 11.0 50 5 65 sulfuric acid: 75 70 1 sodium 40 5 66 10 hydroxide 40 5 67 30 pH 12.1 40 5 68 sulfuric acid: 150 40 1 sodium 50 20 69 10 carbonate 50 20 70 30 pH 10.3 50 20 71 sulfuric acid: 200 40 1 sodium 60 30 72 10 hydrogen 60 30 73 30 carbonate 60 30 pH 9.6 74 nitric acid: 150 + 8.2 40 10 hydrochloric acid: 5 + 40 1 sodium 40 10 75 hydrochloric sulfuric acid: 5 10 hydrogen 40 10 76 acid: 15 30 carbonate 40 10 pH 9.6 77 nitric acid: 150 + 7.3 40 10 hydrochloric acid: 10 + 40 1 sodium 40 10 78 hydrochloric sulfuric acid: 50 10 hydrogen 40 10 79 acid: 15 30 carbonate 40 10 pH 9.6 80 nitric acid: 50 + 10.1 40 10 hydrochloric acid: 5 + 40 1 sodium 40 10 81 hydrofluoric sulfuric acid: 5 10 hydrogen 40 10 82 acid: 50 30 carbonate 40 10 pH 9.6 Total width of peeling after corrosion test (mm) Surface characteristic Temperature of chemical conversion treatment solution Surface coverage of Generation of spot rust 35° C. 33° C. iron-based oxide not present: ∘ Hot brine Salt water Compound cycle No (%) present: x dipping test spraying test corrosion test Remarks 38 39.4 ∘ 4.9 4.1 5.8 5.8 our example 39 35.2 ∘ 4.8 4.0 5.5 5.7 our example 40 30.3 ∘ 4.6 3.8 5.2 5.3 our example 41 38.9 ∘ 4.7 4.1 5.8 5.9 our example 42 35.9 ∘ 4.6 3.9 5.5 5.7 our example 43 31.2 ∘ 4.4 3.6 5.4 5.3 our example 44 34.9 ∘ 4.7 3.7 5.5 5.7 our example 45 30.2 ∘ 4.6 3.8 5.3 5.3 our example 46 25.8 ∘ 4.2 3.5 4.9 4.9 our example 47 30.8 ∘ 4.5 3.6 5.3 5.5 our example 48 25.0 ∘ 4.2 3.4 4.6 4.9 our example 49 22.6 ∘ 4.0 3.2 4.4 4.7 our example 50 30.3 ∘ 4.5 3.4 5.3 5.5 our example 51 25.9 ∘ 4.3 3.1 4.5 4.9 our example 52 21.0 ∘ 4.1 3.1 4.1 4.6 our example 53 49.9 ∘ 5.3 4.3 6.5 6.8 our example 54 55.1 ∘ 5.7 4.7 7.2 7.3 our example 55 62.3 ∘ 5.9 5.1 7.5 7.6 our example 56 39.6 ∘ 5.1 3.9 5.8 6.2 our example 57 36.2 ∘ 4.8 3.7 5.6 5.9 our example 58 32.5 ∘ 4.7 3.5 5.5 5.7 our example 59 39.1 ∘ 4.8 4.1 5.9 6.2 our example 60 37.0 ∘ 4.7 4.0 5.7 5.9 our example 61 33.7 ∘ 4.6 3.8 5.5 5.7 our example 62 36.1 ∘ 4.8 3.9 5.6 5.8 our example 63 32.5 ∘ 4.7 3.5 5.4 5.6 our example 64 28.4 ∘ 4.5 3.5 4.9 5.3 our example 65 32.3 ∘ 4.6 3.6 5.4 5.6 our example 66 26.7 ∘ 4.3 3.4 4.6 5.0 our example 67 24.5 ∘ 4.3 3.1 4.5 4.9 our example 68 31.2 ∘ 4.6 3.5 5.1 5.2 our example 69 25.5 ∘ 4.3 3.5 4.9 5.1 our example 70 22.1 ∘ 4.1 3.6 4.4 4.8 our example 71 50.3 ∘ 5.3 4.5 6.5 6.7 our example 72 55.7 ∘ 5.7 4.7 7.3 7.5 our example 73 61.3 ∘ 5.8 5.1 7.5 7.5 our example 74 35.4 ∘ 4.6 3.8 5.5 5.9 our example 75 30.5 ∘ 4.3 3.9 4.9 5.0 our example 76 26.1 ∘ 3.9 3.3 4.5 4.7 our example 77 33.1 ∘ 4.3 3.5 5.2 5.7 our example 78 31.1 ∘ 4.1 3.5 4.8 5.2 our example 79 25.7 ∘ 3.9 3.4 4.7 4.8 our example 80 35.5 ∘ 4.5 3.7 5.3 5.5 our example 81 30.8 ∘ 4.5 3.5 4.8 5.2 our example 82 26.9 ∘ 4.2 3.3 4.6 4.9 our example

From Table 2, it is understood that our steel sheets where pickling was performed under the conditions which conform to our method after continuous annealing exhibit favorable chemical convertibility and favorable corrosion resistance after coating such that the generation of spot rust is suppressed, and the maximum total width of peeling is small in all of the hot brine dipping test, the salt water spraying test and the composite cycle corrosion test. Particularly, it is understood that all cold-rolled steel sheets where a surface coverage of an iron-based oxide is 40% or less exhibit excellent corrosion resistance after coating in a severe corrosion environment. It is ascertained from the result obtained by measuring the distribution of O, Si, Mn and Fe in the depth direction in surfaces of the respective steel sheets in Table 2 by a GDS that a peak of Si and a peak of O did not appear in the steel sheets which were subjected to pickling under the conditions which conform to our method so that an Si containing oxide layer was sufficiently removed. As references, profiles of O, Si, Mn and Fe in the depth direction when a surface analysis was performed by the GDS with respect to our specimens of example Nos. 2 and 7 in Table 2 are shown in FIGS. 5A and 5B.

Example 2

Steels A to O containing compositions shown in Table 3 were manufactured such that molten steel was produced by an ordinary refining process including a converter treatment, a degassing treatment and the like, and molten steel was formed into steel slabs by continuous casting. Hot rolling was applied to these steel slabs under hot rolling conditions shown in Table 4, and the steel slabs are formed into hot-rolled steel sheets having a thickness of 3 to 4 mm, scales were removed from surfaces of the steel sheets by applying pickling to these hot-rolled steel sheets and, thereafter, cold rolling was applied to the steel sheets thus obtaining cold-rolled steel sheets having a thickness of 1.8 mm. Next, after first pickling and second pickling were applied to the cold-rolled steel sheet under conditions shown in Table 5 after continuous annealing performed under conditions shown in Table 4 in the same manner, the steel sheet was cleaned with water, and neutralizing treatment was applied to the steel sheet, water cleaning and drying were applied to the steel sheet. Temper rolling with elongation of 0.7% was applied to the steel sheet thus obtaining cold-rolled steel sheets No. 84 to No. 107.

Specimens were sampled from the above-mentioned respective cold rolled steel sheets obtained in the same manner as the example 1, and, after surface coverage of the iron-based oxide on the surface of the steel sheet after pickling was measured, the specimen is subjected to the following tensile test and the corrosion resistance test after coating. Further, the distribution of O, Si, Mn and Fe in the depth direction on surfaces of the specimens sampled from the respective cold-rolled steel sheets was measured using a GDS.

(1) Mechanical Characteristic

A tensile test is performed in accordance with the stipulation of JIS Z 2241: 1998 using a JIS No. 5 tensile test specimen (n=1) stipulated in JIS Z 2201: 1998 sampled from a direction orthogonal to the rolling direction (C direction) thus measuring a tensile strength TS.

(2) Spot Rust Generation Evaluation During Storage of Cold-Rolled Steel Sheets

After anti-rust oil was applied to the above-mentioned respective cold-rolled steel sheets, the cold-rolled steel sheets were left outdoors while preventing influences from external factors such as dusts. Presence or non-presence of generation of spot rust on the cold-rolled steel sheets after approximately one month was checked. The evaluation “0” is given to cases where the specimens had no spot rust, and the evaluation “X” is given to cases where the specimens had spot rust.

(3) Corrosion Resistance after Coating

Specimens were prepared by applying chemical conversion treatment and electrodeposition coating to specimens sampled from the respective cold-rolled steel sheet under the same condition as the example 1. In the same manner as the example 1, the specimens were subjected to three kinds of corrosion tests consisting of a hot brine dipping test, a salt water spraying test (SST) and a composite cycle corrosion test (CCT) and, then, the corrosion resistance after coating was evaluated.

The result of the above-mentioned test is shown in Table 5.

TABLE 3 Steel Steel component (mass. %) symbol C Si Mn P S Al Si/Mn Remarks A 0.11 1.25 1.55 0.018 0.001 0.032 0.81 our steel B 0.15 1.30 1.80 0.019 0.002 0.033 0.72 our steel C 0.15 1.20 1.95 0.017 0.001 0.033 0.62 our steel D 0.09 1.45 1.40 0.017 0.002 0.028 1.04 our steel E 0.18 1.11 1.36 0.018 0.001 0.032 0.82 our steel F 0.16 1.41 1.23 0.017 0.001 0.041 1.15 our steel G 0.14 1.65 1.33 0.018 0.002 0.035 1.24 our steel H 0.12 1.45 2.10 0.017 0.001 0.042 0.69 our steel I 0.17 0.90 1.40 0.017 0.002 0.044 0.64 our steel J 0.13 1.20 1.89 0.018 0.001 0.041 0.63 our steel K 0.15 1.20 1.85 0.017 0.001 0.034 0.65 our steel L 0.03 1.25 3.25 0.018 0.001 0.005 0.38 our steel M 0.22 3.30 1.15 0.018 0.001 0.027 2.87 our steel Steel Steel component (mass. %) symbol C Si Mn P S Al Nb Ti V Mo N 0.13 1.13 1.25 0.023 0.006 0.052 0.11 0.05 0.04 0.05 O 0.11 1.12 1.26 0.031 0.004 0.026 0.01 0.01 0.01 0.01 Steel Steel component (mass. %) symbol Cr B N Ni Cu Ca Si/Mn Remarks N 0.06 0.007 0.007 0.01 0.01 0.01 0.90 our steel O 0.01 0.01 0.01 0.21 0.25 0.018 0.89 our steel

TABLE 4 Hot rolling condition Continuous annealing condition Heating Finish Cooling Winding Cold Heating Hold- Cooling Cooling stop Hold- Cooling temper- temper- rate temper- rolling temper- ing rate temper- ing rate Strength Steel ature ature (° C./ ature reduction ature time (° C./ ature time (° C./ TS No symbol (° C.) (° C.) sec.) (° C.) (%) (° C.) (sec.) sec.) (° C.) (sec.) sec.) (MPa) Remarks 86 A 1150 850 25 620 60 780 45 20 350 100 40 625 our example 87 B 1150 820 31 400 60 780 40 20 400 100 50 821 our example 88 B 1150 820 31 400 60 780 40 20 400 100 50 819 our example 89 C 1140 850 26 600 60 760 50 20 350 100 45 814 our example 90 D 1150 840 33 530 60 730 40 20 350 110 40 623 our example 91 E 1150 850 30 580 55 750 35 20 400 110 50 836 our example 92 F 1150 850 25 620 60 750 50 20 350 120 50 634 our example 93 G 1150 850 33 550 60 750 30 20 400 100 50 632 comparison example 94 G 1150 850 33 550 60 750 30 20 400 100 50 635 our example 95 G 1150 850 33 550 60 750 30 20 400 100 50 631 our example 96 G 1150 850 33 550 60 750 30 20 400 100 50 633 our example 97 G 1150 850 33 550 60 750 30 20 400 100 50 634 comparison example 98 H 1130 820 28 570 60 780 50 15 370 150 50 840 our example 99 I 1150 840 34 530 55 780 50 15 350 120 55 812 our example 100 J 1140 850 28 600 60 770 60 20 300 100 45 836 our example 101 K 1150 850 25 620 60 780 45 20 350 100 40 650 our example 102 L 1100 850 33 550 60 750 50 20 450 150 50 960 comparison example 103 L 1100 850 33 550 60 750 50 20 450 150 50 959 our example 104 L 1100 850 33 550 60 750 50 20 450 150 50 963 our example 105 L 1100 850 33 550 60 750 50 20 450 150 50 962 our example 106 L 1100 850 33 550 60 750 50 20 450 150 50 961 comparison example 107 M 1120 830 31 550 55 720 50 15 410 190 50 1124 comparison example 84 N 1150 850 30 580 55 750 35 20 400 110 50 828 our example 85 O 1150 850 30 580 55 750 35 20 400 110 50 828 our example

TABLE 5 First pickling condition Second pickling condition Neutralization condition Fe ion Treat- Treat- Treat- Acid concen- Temper- ment Acid Temper- ment Temper- ment Steel concentration tration ature time concentration ature time ature time No symbol (g/l) (g/l) (° C.) (sec.) (g/l) (° C.) (sec.) Alkali pH (° C.) (sec.) 86 A nitric acid: 150 + 12.1 40 10 hydrochloric acid: 10 40 10 sodium 40 10 87 B hydrochloric 40 10 hydrochloric acid: 10 40 10 pyrophosphate 40 10 acid: 15 pH 11.0 88 B nitric acid: 50 + 7.8 40 10 hydrochloric acid: 10 40 10 40 10 hydrofluoric acid: 50 89 C nitric acid: 150 + 8.3 40 10 hydrochloric acid: 10 40 10 40 10 90 D hydrochloric 40 10 hydrochloric acid: 10 40 10 40 10 91 E acid: 15 40 10 hydrochloric acid: 10 40 10 40 10 92 F 40 10 hydrochloric acid: 10 40 10 40 10 93 G 40 10 hydrochloric acid: 10 10 1 — — — 94 G 40 10 hydrochloric acid: 10 40 1 sodium 40 10 95 G 40 10 hydrochloric acid: 10 40 30 polyphosphate 40 10 96 G 40 10 sulfuric acid: 75 40 30 pH 9.7 40 10 97 G 40 10 hydrochloric acid: 100 40 10 — — — 98 H 40 10 hydrochloric acid: 10 40 10 sodium 40 10 99 I 40 10 hydrochloric acid: 10 40 10 carbonate 40 10 100 J 40 10 hydrochloric acid: 10 40 10 pH 10.3 40 10 101 K 40 10 hydrochloric acid: 10 40 10 40 10 102 L 40 10 sulfuric acid: 75 10 1 — — — 103 L 40 10 sulfuric acid: 75 40 1 sodium 40 10 104 L 40 10 sulfuric acid: 75 40 30 hydrogen 40 10 105 L 40 10 hydrochloric acid: 10 40 30 carbonate 40 10 pH 9.6 106 L 40 10 sulfuric acid: 200 40 10 — — — 107 M 40 10 hydrochloric acid: 10 40 10 — — — 84 N Nitric acid: 150 + 8.2 40 10 hydrochloric acid: 10 40 10 sodium 40 40 85 O hydrochloric 10 10 hydrochloric acid: 10 40 10 pyrophosphate 10 10 acid: 15 pH 9.9 Total width of peeling after corrosion test (mm) Surface characteristic Temperature of chemical conversion Surface coverage of Generation of spot rust treatment solution: 35° C. 33° C. iron-based oxide not present: ∘ Hot brine Salt water Compound cycle No (%) present: x dipping test spraying test corrosion test Remarks 86 29.9 ∘ 4.5 3.8 4.7 5.0 our example 87 30.4 ∘ 4.4 3.8 4.5 5.1 our example 88 30.1 ∘ 4.4 3.7 4.9 5.2 our example 89 29.7 ∘ 4.4 3.6 4.6 5.1 our example 90 30.5 ∘ 4.5 3.8 4.7 5.2 our example 91 30.3 ∘ 4.4 3.9 4.7 5.2 our example 92 30.2 ∘ 4.3 3.6 4.8 5.1 our example 93 74.3 x 6.5 5.3 7.7 8.0 comparison example 94 35.4 ∘ 4.4 3.8 5.1 5.4 our example 95 25.9 ∘ 4.2 3.5 4.6 4.7 our example 96 26.3 ∘ 4.1 3.2 4.7 4.8 our example 97 54.5 x 5.7 4.7 7.1 7.4 comparison example 98 30.3 ∘ 4.3 3.8 4.9 5.1 our example 99 30.9 ∘ 4.3 3.7 4.9 5.1 our example 100 30.1 ∘ 4.3 3.8 4.9 5.1 our example 101 29.7 ∘ 4.2 3.8 4.6 5.0 our example 102 75.2 x 6.4 5.5 7.8 8.2 comparison example 103 34.9 ∘ 4.5 3.8 5.2 5.3 our example 104 25.3 ∘ 4.4 3.5 4.9 5.2 our example 105 25.4 ∘ 4.2 3.1 5.1 5.1 our example 106 55.0 x 5.7 4.7 7.1 7.4 comparison example 107 41.2 x 5.2 4.1 6.3 6.5 comparison example 84 27.3 ∘ 4.3 3.8 4.7 5.2 our example 85 26.2 ∘ 4.4 3.9 4.6 5.3 our example

It is understood from Table 5 that the high strength cold-rolled steel sheet of our example where the steel sheet contains 0.5% or more Si, and a surface coverage of iron-based oxide on the surface of the steel sheet to which neutralizing treatment is performed by applying pickling twice under the condition which conforms to our method is set to 40% or less not only is excellent in chemical convertibility and corrosion resistance after coating but also has a high strength of 590 MPa or more of tensile strength TS. It is ascertained from the result obtained by measuring the distribution of O, Si, Mn and Fe in the depth direction by a GDS that a peak of Si and a peak of O did not appear in any steel sheets which were subjected to pickling under the conditions which conform to our method so that an Si containing oxide layer was sufficiently removed.

Example 3

Steel having the composition containing 0.125% C, 1.5% Si, 2.6% Mn, 0.019% P, 0.008% S and 0.040% Al and comprising Fe and unavoidable impurities as a balance was manufactured such that molten steel was formed into steel materials (slabs) by continuous casting. The slabs were reheated to a temperature of 1150 to 1170° C. and, thereafter, were subjected to hot rolling where a finish rolling completion temperature is set to 850 to 880° C., and were wound up at a temperature of 500 to 550° C. thus forming hot-rolled steel sheets having a thickness of 3 to 4 mm. Scales were removed from the steel sheets by applying pickling to these hot-rolled steel sheets and, thereafter, cold rolling was applied to the steel sheets thus obtaining cold-rolled steel sheets having a thickness of 1.8 mm. Next, continuous annealing was performed where these cold-rolled steel sheets were heated to a soaking temperature of 750 to 780° C. and were held for 40 to 50 seconds and, thereafter, these steel sheets were cooled to a cooling stop temperature of 350 to 400° C. from the above-mentioned soaking temperature at a cooling rate of 20 to 30° C./second and were held for 100 to 120 seconds at a cooling stop temperature range. Thereafter, first pickling and second pickling were applied to surfaces of the steel sheets under conditions shown in Table 6-1 to Table 6-2 (hereinafter, Table 6-1 and Table 6-2 being also collectively referred to as Table 6) and, then, the steel sheets were washed with water, neutralizing treatment was applied to the steel sheets, and the steel sheets were washed with water and were dried. Thereafter, temper rolling was applied to the steel sheets at a rate of elongation of 0.7% thus obtaining cold-rolled steel sheets No. 108 to No. 162 shown in Table 6.

Specimens were sampled from the above-mentioned respective cold-rolled steel sheets and, using the above-mentioned method, a surface coverage of iron-based oxide generated on the surface of the steel sheets by pickling and a maximum thickness were measured.

Further, specimens were sampled from the above-mentioned respective cold-rolled steel sheets, and spot rust generation evaluation during storage of the cold-rolled steel sheets was carried out under the following conditions and, after a chemical conversion treatment and a coating treatment were applied to the specimens under the following conditions, specimens were subjected to three kinds of corrosion tests consisting of a hot brine dipping test, a salt water spraying test and a composite cycle corrosion test, and then, the corrosion resistance after coating was evaluated. Further, the distribution of O, Si, Mn and Fe in the depth direction on surfaces of the specimens sampled from the respective cold-rolled steel sheets was measured using a GDS.

(1) Spot Rust Generation Evaluation During Storage of Cold-Rolled Steel Sheets

After anti-rust oil was applied to the above-mentioned respective cold-rolled steel sheets, the cold-rolled steel sheets were left outdoors while preventing influences from external factors such as dusts. Presence or non-presence of generation of spot rust on the cold-rolled steel sheets after approximately one month was checked. The evaluation “0” is given to cases where the specimens had no spot rust, and the evaluation “X” is given to cases where the specimens had spot rust.

(2) Chemical Conversion Treatment Condition

A chemical conversion treatment was applied to specimens sampled from the above-mentioned respective cold-rolled steel sheets using a degreasing agent FC-E2011, a surface conditioner: PL-X and a chemical conversion treatment agent: palbond PB-L3065 made by Nihon Parkerizing Co., Ltd. such that a coating weight of chemical conversion treatment film was set to 1.7 to 3.0 g/m2 under two conditions, that is, the standard condition and the comparison condition under a low temperature by lowering a temperature of a chemical conversion treatment solution.

Standard Condition

Degreasing step: treatment temperature 40° C., treatment time 120 seconds Spray degreasing and surface adjustment steps: pH 9.5, treatment temperature room temperature, treatment time 20 seconds
Chemical conversion treatment step: temperature of chemical conversion treatment solution 35° C., treatment time 120 seconds

Temperature Lowering Condition

Condition where a temperature of chemical conversion treatment solution in the above-mentioned standard condition was lowered to 33° C.

(3) Corrosion Test

Electrodeposition coating was applied to surfaces of the specimens to which the above-mentioned chemical conversion treatment had been applied by electrodeposition paint: V-50 made by NIPPONPAINT Co., Ltd. such that a film thickness of electrodeposition coating is set to 25 μm, and the specimens were subjected to the following three kinds of corrosion tests under more severe condition than the example 1.

Hot Brine Dipping Test

A crosscut flaw having a length of 45 mm is formed by a cutter on a surface of the above-mentioned specimen (n=1) to which chemical conversion treatment and electrodeposition coating were applied and thereafter, the specimen was dipped into 5 mass % NaCl aqueous solution (60° C.) for 480 hours. Then, the specimen was cleaned with water, was dried, and an adhesive tape was adhered to the cut flaw portion. Thereafter, a tape peeling test in which the adhesive tape is peeled was performed, and a maximum total width of peeling including left and right sides of the cut flaw portion was measured. When the maximum peeling total width is 6.0 mm or less, it is determined that the specimen is not defective. When the maximum peeling total width is 5.0 mm or less, it can be evaluated that corrosion resistance of the specimen in the hot brine dipping test is favorable.

Salt Water Spraying Test (SST)

A crosscut flaw having a length of 45 mm is formed by a cutter on a surface of the above-mentioned specimen (n=1) to which chemical conversion treatment and electrodeposition coating were applied and, thereafter, the specimen was subjected to a salt water spraying test for 1400 hours in accordance with a neutral salt water spraying test stipulated in JIS Z2371:2000 using 5 mass % NaCl aqueous solution. Thereafter, a tape peeling test was carried out with respect to the crosscut flaw portion, and a maximum total width of peeling including left and right sides of the cut flaw portion was measured. When the maximum total width of peeling is 5.2 mm or less, it is determined that the specimen is not defective. When the maximum total width of peeling is 4.0 mm or less, it can be evaluated that corrosion resistance of the specimen in the salt water spraying test is favorable.

Composite Cycle Corrosion Test (CCT)

A crosscut flaw having a length of 45 mm is formed by a cutter on a surface of the above-mentioned specimen (n=1) to which chemical conversion treatment and electrodeposition coating were applied and, thereafter, the specimen was subjected to a corrosion test where one cycle formed of salt water spraying (5 mass % NaCl aqueous solution: 35° C., relative humidity: 98%)×2 hours→drying (60° C., relative humidity: 30%)×2 hours→wetting (50° C., relative humidity: 95%)×2 hours was repeated 150 times, was cleaned with water and, thereafter, was dried. Then, a tape peeling test was carried out with respect to the cut flaw portion, and a maximum total width of peeling including left and right sides of the cut flaw portion was measured. When the maximum total width of peeling is 7.8 mm or less, it is determined that specimen is not defective. When the maximum total width of peeling is 6.0 mm or less, it can be evaluated that the corrosion resistance of the specimen in the composite cycle corrosion test is favorable.

The result of the above-mentioned test is shown in Table 6.

TABLE 6 First pickling condition Fe ion Second pickling condition Neutralization condition Acid concen- Temper- Treatment Acid Temper- Treatment Temper- Treatment concentration tration ature time concentration ature time ature time No (g/l) (g/l) (° C.) (sec.) (g/l) (° C.) (sec.) Alkali pH (° C.) (sec.) 108 nitric acid: 150 + 12.9 40 10 — — — — — — 109 hydrochloric 40 10 hydrochloric 40 1 sodium 30 20 110 acid: 15 acid: 0.1 10 polyphosphate 30 20 111 30 pH 9.7 30 20 112 40 10 hydrochloric 40 1 sodium 50 5 113 acid: 3 10 carbonate 50 5 114 30 pH 10.3 50 5 115 40 10 hydrochloric 40 1 sodium 40 10 116 acid: 10 10 pyrophosphate 40 10 117 30 pH 11.0 40 10 118 40 10 hydrochloric 40 1 sodium hydrogen 60 10 119 acid: 50 10 carbonate 60 10 120 30 pH 9.6 60 10 121 nitric acid: 50 + 8.3 40 10 hydrochloric 40 1 sodium 30 20 122 hydrofluoric acid: 0.1 10 polyphosphate 30 20 123 acid: 50 30 pH 9.7 30 20 124 40 10 hydrochloric 40 1 sodium 50 5 125 acid: 3 10 carbonate 50 5 126 30 pH 10.3 50 5 127 40 10 hydrochloric 40 1 sodium 40 10 128 acid: 10 10 pyrophosphate 40 10 129 30 pH 11.0 40 10 130 40 10 hydrochloric 40 1 sodium hydrogen 60 10 131 acid: 50 10 carbonate 60 10 132 30 pH 9.6 60 10 Total width of peeling after corrosion test (mm) Surface characteristic Temperature of chemical conversion Surface coverage of Maximum thickness of Generation of spot rust treatment solution: 35° C. 33° C. iron-based oxide iron-based oxide not present: ∘ Hot brine Salt water Compound cycle No (%) (nm) present: x dipping test spraying test corrosion test Remarks 108 72.6 214 x 6.5 5.8 8.2 8.4 comparison example 109 39.3 156 ∘ 4.8 4.2 5.9 5.9 our example 110 35.2 156 ∘ 4.9 4.1 5.8 5.8 our example 111 30.1 161 ∘ 4.8 4.1 5.8 5.9 our example 112 38.1 148 ∘ 4.8 4.2 5.8 5.7 our example 113 33.2 147 ∘ 4.8 4.1 5.9 5.8 our example 114 27.6 143 ∘ 4.9 4.2 5.7 5.9 our example 115 35.1 119 ∘ 4.7 4.1 5.3 5.8 our example 116 30.1 113 ∘ 4.6 3.9 5.6 5.6 our example 117 26.2 123 ∘ 4.9 4.1 5.5 5.5 our example 118 30.3  92 ∘ 4.5 3.7 5.3 5.4 our example 119 26.3  86 ∘ 4.3 3.5 4.8 5.3 our example 120 21.5  85 ∘ 4.4 3.4 4.7 4.6 our example 121 39.5 163 ∘ 5.4 4.3 6.2 6.1 our example 122 36.3 165 ∘ 5.5 4.5 6.3 6.3 our example 123 32.7 158 ∘ 5.3 4.3 6.3 6.3 our example 124 37.9 147 ∘ 5.1 4.2 5.8 6.2 our example 125 34.3 146 ∘ 4.7 4.2 5.7 6.0 our example 126 28.3 147 ∘ 4.9 4.1 5.9 5.9 our example 127 35.9 145 ∘ 4.8 4.0 5.8 6.0 our example 128 33.1 143 ∘ 4.7 4.2 5.7 5.9 our example 129 28.1 147 ∘ 4.8 4.2 5.8 6.1 our example 130 32.1 116 ∘ 4.7 4.1 5.6 5.6 our example 131 26.1 119 ∘ 4.5 3.9 5.5 5.6 our example 132 22.5 117 ∘ 4.4 3.9 5.5 5.4 our example First pickling condition Fe ion Second pickling condition Neutralization condition Acid concen- Temper- Treatment Acid Temper- Treatment Temper- Treatment concentration tration ature time concentration ature time ature time No (g/l) (g/l) (° C.) (sec.) (g/l) (° C.) (sec.) Alkali pH (° C.) (sec.) 133 nitric acid: 150 + 7.9 40 10 sulfuric acid: 0.1 40 1 sodium 30 20 134 hydrochloric 10 polyphosphate 30 20 135 acid: 15 30 pH 9.7 30 20 136 sulfuric acid: 8 40 1 sodium carbonate 50 5 137 10 pH 10.3 50 5 138 30 50 5 139 sulfuric acid: 75 40 1 sodium 40 10 140 10 pyrophosphate 40 10 141 30 pH 11.0 40 10 142 sulfuric acid: 150 40 1 sodium hydrogen 60 10 143 10 carbonate 60 10 144 30 pH 9.6 60 10 145 nitric acid: 50 + 6.6 40 10 sulfuric acid: 0.1 40 1 sodium 30 20 146 hydrofluoric 10 polyphosphate 30 20 147 acid: 50 30 pH 9.7 30 20 148 sulfuric acid: 8 40 1 sodium carbonate 50 5 149 10 pH 10.3 50 5 150 30 50 5 151 sulfuric acid: 75 40 1 sodium 40 10 152 10 pyrophosphate 40 10 153 30 pH 11.0 40 10 154 sulfuric acid: 150 40 1 sodium hydrogen 60 10 155 10 carbonate 60 10 156 30 pH 9.6 60 10 157 nitric acid: 150 + 7.9 40 10 hydrochloric acid: 5 + 40 1 sodium hydrogen 40 10 158 hydrochloric sulfuric acid: 5 10 carbonate 40 10 159 acid: 15 30 pH 9.6 40 10 160 nitric acid: 50 + 5.9 40 10 hydrochloric acid: 5 + 40 1 sodium hydrogen 40 10 161 hydrofluoric sulfuric acid: 10 10 carbonate 40 10 162 acid: 50 30 pH 9.6 40 10 Total width of peeling after corrosion test (mm) Surface characteristic Temperature of chemical conversion Surface coverage of Maximum thickness of Generation of spot rust treatment solution: 35° C. iron-based oxide iron-based oxide not present: ∘ Hot brine Salt water Compound cycle No (%) (nm) present: x dipping test spraying test corrosion test Remarks 133 39.4 158 ∘ 4.8 4.2 5.7 5.8 our example 134 35.1 155 ∘ 4.8 4.1 5.7 5.6 our example 135 30.1 161 ∘ 4.7 4.0 5.6 5.8 our example 136 37.9 149 ∘ 4.7 4.1 5.4 5.9 our example 137 33.3 145 ∘ 4.6 3.9 5.9 5.8 our example 138 28.1 148 ∘ 4.8 3.9 5.6 5.8 our example 139 35.1 121 ∘ 4.7 4.2 5.7 5.6 our example 140 30.7 117 ∘ 4.6 3.9 5.4 5.5 our example 141 25.6 115 ∘ 4.5 3.7 5.5 5.7 our example 142 30.3 89 ∘ 4.6 3.8 5.3 5.3 our example 143 26.5 83 ∘ 4.5 3.7 5.0 5.3 our example 144 21.5 85 ∘ 4.4 3.5 5.1 5.2 our example 145 39.4 166 ∘ 5.3 4.4 6.3 6.1 our example 146 36.3 163 ∘ 5.5 4.1 6.2 6.4 our example 147 32.7 162 ∘ 5.4 4.2 6.2 6.2 our example 148 37.7 148 ∘ 4.9 4.2 5.8 6.1 our example 149 33.6 146 ∘ 4.8 3.9 5.7 5.9 our example 150 27.5 147 ∘ 5.1 3.9 5.7 5.8 our example 151 35.9 143 ∘ 4.8 4.1 5.9 5.9 our example 152 32.6 145 ∘ 4.7 3.8 5.8 6.1 our example 153 28.6 146 ∘ 4.8 3.7 5.8 6.2 our example 154 31.3 116 ∘ 4.7 3.6 5.6 5.7 our example 155 25.7 112 ∘ 4.6 3.9 5.5 5.8 our example 156 22.6 115 ∘ 4.6 3.6 5.4 5.6 our example 157 35.3 153 ∘ 4.7 3.7 5.7 5.9 our example 158 30.7 154 ∘ 4.6 3.6 5.8 6.0 our example 159 26.5 154 ∘ 4.8 3.6 5.5 5.8 our example 160 35.4 138 ∘ 4.7 3.6 5.7 5.8 our example 161 30.5 142 ∘ 4.7 3.8 5.7 5.6 our example 162 27.3 135 ∘ 4.6 3.6 5.8 5.7 our example

It is understood from Table 6 that the steel sheet of our example where pickling is applied to the surface of the steel sheet after annealing under a condition that a surface coverage of iron-based oxide on the surface of the steel plate after re-pickling is set to 40% or less, and a maximum thickness of the iron-based oxide is 150 nm or less had a small maximum total width of peeling in any of the hot brine dipping test, the salt water spraying test and the composite cycle corrosion test which were performed under the conditions where the test times were long and the test environments were severe compared to the example 1 and, hence, the steel sheets exhibit extremely favorable corrosion resistance after coating. Further, it is ascertained from the result obtained by measuring the distribution of O, Si, Mn and Fe in the depth direction by a GDS that a peak of Si and a peak of O did not appear in the steel sheets which were subjected to pickling under the conditions which conform to our method so that an Si containing oxide layer was sufficiently removed.

INDUSTRIAL APPLICABILITY

Our cold-rolled steel sheet can possess not only excellent chemical convertibility and corrosion resistance after coating but also a high strength and hence, the cold-rolled steel sheet can be preferably used as a raw material for forming automobile members and also as a raw material for forming members which are required to possess the substantially similar property as the automobile member in other fields such as household electric appliances and architecture.

Claims

1.-19. (canceled)

20. A method of manufacturing a cold-rolled steel sheet, wherein first pickling is applied to a steel sheet which is continuously annealed after cold rolling, second pickling is applied to the steel sheet subsequently and, thereafter, neutralizing treatment is applied to the steel sheet using an alkaline solution.

21. The method according to claim 20, wherein the alkaline solution has pH of 9.5 or more, and one or two or more selected from a group consisting of sodium hydroxide, sodium carbonate, sodium hydrogen carbonate, orthophosphate and condensed phosphate are mixed into the alkaline solution.

22. The method according to claim 20, wherein the neutralizing treatment is performed in a state that a temperature of the alkaline solution is set to 20 to 70° C., and a treatment time is set to 1 to 30 seconds.

23. The method according to claim 20, wherein the first pickling is performed using any one of a nitric acid, a hydrochloric acid, a hydrofluoric acid, a sulfuric acid and a mixture of two or more thereof.

24. The method according to claim 20, wherein the first pickling is performed using either one of the following acidic solutions (a) and (b):

(a) the acidic solution containing a nitric acid and a hydrochloric acid, wherein concentration of the nitric acid is more than 50 g/L and 200 g/L or less, a ratio R1 of the concentration of the hydrochloric acid to a concentration of the nitric acid (hydrochloric acid/nitric acid) is set to 0.01 to 0.25, and a concentration of Fe ion is set to 3 to 50 g/L.
(b) the acidic solution containing a nitric acid and hydrofluoric acid, wherein concentration of the nitric acid is more than 50 g/L and 200 g/L or less, a ratio R2 of the concentration of the hydrofluoric acid to a concentration of the nitric acid (hydrofluoric acid/nitric acid) is set to 0.01 to 0.25, and a concentration of Fe ion is set to 3 to 50 g/L.

25. The method according to claim 20, wherein a non-oxidizing acid is used in the second pickling.

26. The method according to claim 25, wherein the non-oxidizing acid is any one of a hydrochloric acid, a sulfuric acid, a phosphoric acid, a pyrophosphoric acid, a formic acid, an acetic acid, a citric acid, a hydrofluoric acid, an oxalic acid, and an acid which is a mixture of two or more of the acids.

27. The method according to claim 25, wherein the non-oxidizing acid is any one of hydrochloric acid having a concentration of 0.1 to 50 g/L, a sulfuric acid having a concentration of 0.1 to 150 g/L and an acid which is a mixture of a hydrochloric acid having a concentration of 0.1 to 20 g/L and a sulfuric acid having a concentration of 0.1 to 60 g/L.

28. The method according to claim 20, wherein the second pickling is performed in a state that a temperature of the acidic solution is set to 20° C. to 70° C., and a pickling time is set to 1 to 30 seconds.

29. The method according to claim 20, wherein the steel sheet contains, as a component of the composition thereof, 0.5 to 3.0 mass % Si.

30. The method according to claim 29, wherein the steel sheet further contains, as components of the composition thereof: 0.01 to 0.30 mass % C, 1.0 to 7.5 mass % Mn, 0.05 mass % or less P, 0.01 mass % or less S, 0.06 mass % or less Al, and Fe and unavoidable impurities as a balance.

31. The method according to claim 30, wherein the steel sheet further contains, as components of the composition thereof, one or two or more of elements selected from a group consisting of 0.3 mass % or less Nb, 0.3 mass % or less Ti, 0.3 mass % or less V, 1.0 mass % or less Mo, 1.0 mass % or less Cr, 0.006 mass % or less B and 0.008 mass % or less N.

32. The method according to claim 30, wherein the steel sheet further contains, as components of the composition thereof, one or two or more of elements selected from a group consisting of 2.0 mass % or less Ni, 2.0 mass % or less Cu, 0.1 mass % or less Ca, and 0.1 mass % or less REM.

33. A cold-rolled steel sheet manufactured by the method of manufacturing a cold-rolled steel sheet described in claim 20, wherein an Si containing oxide layer formed on a surface layer of the steel sheet is removed, and a surface coverage of an iron-based oxide existing on a surface of the steel sheet is 40% or less.

34. The cold-rolled steel sheet according to claim 33, wherein a maximum thickness of the iron-based oxide existing on the surface of the steel sheet is 150 nm or less.

35. An automobile member formed by using the cold-rolled steel sheet described in claim 33.

36. A facility for manufacturing a cold-rolled steel sheet, wherein a first pickling device, a second pickling device, an acid neutralizing treatment device, and a drying device are arranged in this order on a rear stage of a continuous annealing device.

37. The facility according to claim 36, further comprising a water cleaning device arranged on a rear stage of the first pickling device, the second pickling device, and the acid neutralizing treatment device.

38. The facility according to claim 36, further comprising a water cleaning spray device arranged on an inlet side and/or an outlet side of one or more devices selected from a group consisting of the first pickling device, the second pickling device, the acid neutralizing treatment device and the water cleaning device.

Patent History
Publication number: 20170306507
Type: Application
Filed: Aug 12, 2015
Publication Date: Oct 26, 2017
Inventors: Hiroyuki Masuoka (Fukuyama), Shoichiro Taira (Tokyo), Shinichi Furuya (Fukuyama)
Application Number: 15/507,601
Classifications
International Classification: C23G 1/00 (20060101); C23G 1/08 (20060101); C23G 1/08 (20060101); C23G 1/08 (20060101); C22C 38/32 (20060101); C22C 38/16 (20060101); C21D 9/46 (20060101); C22C 38/12 (20060101); C22C 38/08 (20060101); C22C 38/06 (20060101); C22C 38/04 (20060101); C22C 38/02 (20060101); C22C 38/00 (20060101); C22C 38/14 (20060101); C23G 1/19 (20060101);