Plated steel plate for hot pressing and hot pressing method of plated steel plate

Abstract

The present invention provides plated steel sheet for hot press use which is excellent in hot lubricity, coating adhesion, spot weldability, and coated corrosion resistance and a method of hot pressing plated steel sheet. The present invention is Plated steel sheet for hot press use and a method of hot pressing plated steel sheet characterized by being plated steel sheet for hot press use which contains an Al plating layer which is formed on one surface or both surfaces of said steel sheet, and a surface coating layer which is formed on said Al plating layer, said surface coating layer containing at least one Zn compound which is selected from a group comprised of Zn hydroxide, Zn phosphate, and a Zn organic acid.

Claims

1. A plated steel sheet for hot press use characterized by being a plated steel sheet for hot press use which contains a steel sheet, an Al plating layer which is formed on one surface or both surfaces of said steel sheet, and a surface coating layer which is formed on said Al plating layer, said surface coating layer consisting of one or more Zn compounds selected from the group consisting of Zn hydroxide and a Zn organic acid and optionally one or both of Zn sulfate and Zn nitrate, and one or more of a resin ingredient, silane coupling agent, or silica in a total ratio of 5 to 30% by mass with respect to a total amount of said one or more Zn compounds, wherein the optional one or both of Zn sulfate and Zn nitrate, as a content of said one or more Zn compounds, are contained in respectively 10 mass % or less, and an amount of deposition of the one or more Zn compounds in said surface coating layer is 0.5 to 7 g/m.sup.2 per surface as Zn.

2. The plated steel sheet for hot press use according to claim 1 characterized in that said Al plating layer contains Si: 3 to 15%.

3. The plated steel sheet for hot press use according to claim 1, wherein the one or more Zn compounds comprise 10% or less, per mass %, of one or both of Zn sulfate and Zn nitrate.

4. The plated steel sheet for hot press use according to claim 2, wherein the one or more Zn compounds comprise 10% or less, per mass %, of one or both of Zn sulfate and Zn nitrate.

5. A method of hot pressing the plated steel sheet of claim 1, comprising: blanking said plated steel sheet; heating the plated steel sheet; and pressing said heated plated steel sheet.

6. The method of hot pressing according to claim 5 characterized in that in the heating before pressing, an average temperature elevation rate is 10 to 300 C./sec at a time when said plated steel sheet is heated by ohmic heating or induction heating from 50 C. to a temperature 10 C. lower than a maximum peak temperature.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is an explanatory view which explains an apparatus for evaluating the hot lubricity of the steel sheet for hot press use of the present invention.

(2) FIG. 2 is an explanatory view which explains the hot lubricity of the steel sheet for hot press use of the present invention.

DESCRIPTION OF EMBODIMENTS

(3) Next, the present invention will be explained in detail.

(4) Plated Steel Sheet for Hot Press Use

(5) First, the plated steel sheet for hot press use of the present invention will be explained. The steel sheet for hot press use of the present invention is comprised of steel sheet on one or both surfaces of which an Al plating layer is formed and on the surface of which Al plating layer a surface coating layer which contains a compound of Zn is further formed.

(6) Steel Sheet Before Plating

(7) As the steel sheet before plating, steel sheet which has a high mechanical strength (meaning tensile strength, yield point, elongation, drawability, hardness, impact value, fatigue strength, creep strength, and other properties relating to mechanical deformation and fracture) is desirably used. One example of the steel sheet before plating which is used for the steel sheet for hot press use of the present invention is shown next.

(8) First, the chemical composition will be explained. Note that, the symbols % mean mass % unless otherwise indicated. The chemical composition of the steel sheet before plating preferably contains, by mass %, C: 0.1 to 0.4%, Si: 0.01 to 0.6%, and Mn: 0.5 to 3%. Furthermore, it preferably contains at least one of Cr: 0.05 to 3.0, V: 0.01 to 1.0%, Mo: 0.01 to 0.3%, Ti: 0.01 to 0.1%, and B: 0.0001 to 0.1%. Further, the balance is comprised of Fe and unavoidable impurities.

(9) C is included to secure the desired mechanical strength. If C is less than 0.1%, a sufficient mechanical strength cannot be obtained. On the other hand, if C exceeds 0.4%, the steel sheet can be hardened, but melt fracture easily occurs. Therefore, the content of C is preferably 0.1 to 0.4%.

(10) Si is an element which improves the mechanical strength. Like C, it is included to secure the desired mechanical strength. If Si is less than 0.01%, the effect of improvement of strength is difficult to secure and a sufficient improvement in mechanical strength cannot be obtained. On the other hand, Si is an easily oxidizable element. Accordingly, if Si exceeds 0.6%, when performing hot dip Al coating, the wettability falls and nonplated parts are liable to be formed. Therefore, the content of Si is preferably made 0.01 to 0.6%.

(11) Mn is an element which improves the mechanical strength and is also an element which improves the hardenability. Furthermore, Mn is effective for preventing hot embrittlement due to the unavoidable impurity S. If Mn is less than 0.5%, these effects cannot be obtained. On the other hand, if Mn exceeds 3%, the residual -phases become too great and the strength is liable to fall. Therefore, the content of Mn is preferably 0.5 to 3%.

(12) Cr, V, and Mo are elements which improve the mechanical properties and are also elements which suppress the formation of pearlite at the time of cooling from the annealing temperature. These effects cannot be obtained if Cr is less than 0.05%, V is less than 0.01%, or Mo is less than 0.01%. On the other hand, if exceeding Cr: 3.0%, V: 1.0%, or Mo: 0.3%, the surface area rate of the hard phases becomes excessive and the shapeability deteriorates.

(13) Ti is an element which improves the mechanical strength and is an element which improves the heat resistance of the Al plating layer. When Ti is less than 0.01%, the effect of improvement of the mechanical strength and oxidation resistance cannot be obtained. On the other hand, if excessively including Ti, carbides and nitrides are formed and the steel is liable to be softened. In particular, when Ti exceeds 0.1%, the desired mechanical strength cannot be obtained. Therefore, the content of Ti is preferably made 0.01 to 0.1%.

(14) B is an element which acts to improve the strength at the time of hardening. If B is less than 0.0001%, such an effect of improvement of strength cannot be obtained. On the other hand, if B exceeds 0.1%, inclusions are formed in the steel sheet causing embrittlement and the fatigue strength is liable to be lowered. Therefore, the content of B is preferably made 0.0001 to 0.1%.

(15) Note that, the above-mentioned chemical composition of the steel sheet before plating is an example. Other chemical compositions are also possible. For example, as a deoxidizing element, Al: 0.001 to 0.08% may also be contained. Further, impurities which end up unavoidably entering in the manufacturing process etc. may also be included.

(16) The steel sheet before plating which has such a chemical composition may be hardened by heating by the hot press method etc. even after plating so as to be given an approximately 1500 MPa or more tensile strength. Even steel sheet which has such a high tensile strength can be easily shaped by the hot press method in the state softened by heating. Further, the shaped product can realize high mechanical strength and, even when made thin for lightening the weight, can be maintained or be improved in mechanical strength.

(17) Al Plating Layer

(18) An Al plating layer is formed on one or both surfaces of the steel sheet before plating. The Al plating layer is, for example, formed on one or both surfaces of the steel sheet by the hot dip method, but the invention is not limited to this.

(19) Further, the chemical composition of the Al plating layer should contain Al: 50% or more. The elements other than Al are not particularly limited, but Si may be proactively included for the following reasons.

(20) If Si is included, an AlFeSi alloy layer is formed at the interface between the plating and the base iron and therefore it is possible to suppress the formation of the brittle AlFe alloy layer which is formed at the time of hot dip coating. If Si is less than 3%, the AlFe alloy layer will grow thick at the stage of performing Al plating, cracking of the plating layer will be assisted at the time of working, and the corrosion resistance may be detrimentally affected. On the other hand, if Si exceeds 15%, conversely the volume rate of the layer which contains Si will increase and the workability of the plating layer or corrosion resistance is liable to fall. Therefore, the Si content in the Al plating layer is preferably made 3 to 15%.

(21) The Al plating layer prevents corrosion of the steel sheet for hot press use of the present invention. Further, when working the steel sheet for hot press use of the present invention by the hot press method, even if heated to a high temperature, the surface will never oxidize and scale (oxides of iron) will never be formed. By using the Al plating layer to prevent the formation of scale, it is possible to eliminate the step of removal of scale, the step of cleaning the surface, the step of treating the surface, etc. and possible to improve the productivity of the shaped product. Further, the Al plating layer is higher in boiling point and melting point than a plating covering comprised of an organic material or a plating covering comprised of another metal-based material (for example, Zn-based material). Therefore, when using the hot press method to shape it, the covering will not evaporate, so shaping at a high temperature becomes possible, the shapeability in hot press forming is further raised, and easy shaping becomes possible.

(22) The heating at the time of hot dip coating and hot pressing can cause the Al plating layer to alloy with the Fe in the steel sheet. Accordingly, the Al plating layer is not necessarily formed in a single layer with a constant chemical composition and will include partially alloyed layers (alloy layers).

(23) Surface Coating Layer

(24) The surface coating layer is formed on the surface of the Al plating layer. The surface coating layer includes one or more Zn compounds which are selected from the group comprised of Zn hydroxide, Zn phosphate, and Zn organic acid. As the Zn compound, Zn hydroxide and Zn phosphate are particularly preferred. As the Zn organic acid, Zn acetate, Zn citrate, Zn oxalate, Zn oleate, and other such Zn salts of carboxylic acids and Zn salts of hydroxyl acids, zinc gluconate, etc. may be mentioned. These compounds have the effect of improving the lubricity at the hot press or reactivity with the chemical conversion solution. Zn hydroxide and Zn phosphate have a small solubility in water, so are used as suspensions, while Zn acetate, which has a large solubility in water, is preferably used as an aqueous solution. Note that, these Zn compounds may contain one or both of Zn sulfate and Zn nitrate, but if exceeding a mass % of 10%, as explained above, the coated corrosion resistance and the weldability are degraded. Therefore, the allowable values of the contents of Zn sulfate and Zn nitrate are preferably 10% or less.

(25) Next, the case where Zn hydroxide is contained in the surface coating layer will be used as an example for the explanation. Zn hydroxide breaks down upon heating to form a smooth coating and results in a better coated corrosion resistance than even with the case of use of ZnO. Note that, even when using a Zn compound other than Zn hydroxide, a surface coating layer is formed in the same way as the case of Zn hydroxide and a similar effect can be obtained.

(26) The surface coating layer which contains Zn hydroxide can be formed, for example, by applying a coating which contains Zn hydroxide and by baking and drying it to harden it after application so as to thereby form a coating film on the Al plating layer. As the method of applying the Zn hydroxide, for example, the method of mixing a suspension which contains Zn hydroxide and a predetermined organic binder and applying it to the surface of the Al plating layer and the method of coating by powder coating etc. may be mentioned. As the predetermined organic binder, for example, a polyurethane-based resin, polyester-based resin, acryl-based resin, silane coupling agent, silica, etc. may be mentioned. These organic binders are made water soluble so as to enable mixing with the suspension of Zn hydroxide. The thus obtained treatment solution is coated on the surface of the Al plated steel sheet.

(27) The Zn hydroxide is not particularly limited in particle size, but is desirably a size of 50 to 1000 nm or so. The particle size of the Zn hydroxide is made the particle size after heat treatment. That is, the particle size after holding at 900 C. in the furnace for 5 to 6 minutes, then rapid cooling in the die is made the one determined by observation by a scan type electron microscope (SEM) etc.

(28) The contents of the resin ingredient, silane coupling agent, silica, and other binder ingredients in the surface coating are preferably, by mass ratio to the Zn hydroxide, together 5 to 30% or so. If the contents of the binder ingredients is less than 5%, the deposition effect is not sufficiently obtained and the coating easily peels off. To stably obtain the deposition effect, the binder ingredient is more preferably made, by mass ratio, 10% or more. On the other hand, even if the content of the binder ingredient exceeds 30%, the effect of deposition becomes saturated and the odor which is produced at the time of heating becomes remarkable, so this is not preferable. The upper limit of the content of the binder ingredient is more preferably made 16%.

(29) The surface coating layer which contains the Zn compound of the present invention is confirmed to have a higher lubricity compared with even the inorganic compound coating, organic compound coating, or composite compound coating which contain at least one of Si, Zr, Ti, and P which are described in PLT 2. For this reason, the shapeability is further improved.

(30) The amount of deposition of Zn hydroxide at the surface coating layer which is formed on the Al plated steel sheet is preferably 0.5 to 7 g/m.sup.2 per surface converted to amount of Zn. If the amount of deposition of Zn hydroxide is 0.5 g/m.sup.2 or more as Zn, as shown in FIG. 2, the lubricity is improved. 1.5 g/m.sup.2 or more is more preferable. On the other hand, if the amount of deposition of Zn hydroxide is over 7 g/m.sup.2 as Zn, the Al plating layer and surface coating layer become too thick and the weldability and paint adhesion fall. Therefore, Zn hydroxide is preferably deposited at the surface coating layer in an amount of 0.5 to 7 g/m.sup.2 as Zn per surface. Furthermore, if considering also the weldability and paint adhesion, the amount of deposition of Zn hydroxide is particularly preferably 0.5 to 2 g/m.sup.2.

(31) Note that, as the method of measurement of the amount of deposition of Zn hydroxide, for example, the fluorescent X-ray method can be utilized. The fluorescent X-ray method uses several types of standard samples with known amounts of deposition of Zn hydroxide so as to prepare a calibration line and converts the Zn intensity of the sample being measured to the amount of deposition of Zn hydroxide.

(32) As the method of baking and drying after applying the treatment solution, for example, the method of using a using a hot air furnace, induction heating furnace, infrared ray furnace, etc. is possible. Further, a method using a combination of these is also possible. At this time, depending on the type of the binder which is included in the treatment solution, instead of baking and drying after application, for example, curing by ultraviolet rays, electron beams, etc. is also possible. As the organic binder, polyurethane or polyester or else acryl or a silane coupling agent etc. may be mentioned. However, the method of forming the surface coating layer of Zn hydroxide is not limited to these examples. Various methods may be used to form the layer.

(33) Note that, when not using a binder, after the treatment solution is applied to the Al plating layer, the surface coating layer is somewhat low in adhesion before curing treatment. If rubbed by a strong force, it may partially peel off.

(34) If the surface coating layer is heated once at the time of hot press forming, it exhibits extremely strong adhesion. PLT 4 discloses to improve the adhesion before hot press forming, but the present invention improves the adhesion after hot press forming. Improvement of adhesion after hot press forming cannot be obtained if including the wurtzite type compound which is disclosed in PLT 4 in the surface coating and is an important characteristic of the present invention. Due to the Zn hydroxide being heated, it is expected that it will be dehydrogenated and partially become Zn oxide etc. and the crystal structure will change. At this time, it is believed that fine particles easily proceed to sinter. In the same way, Zn phosphate and Zn organic acid also are believed to break down upon being heated. A compound with a low solubility in water such as Zn hydroxide and Zn phosphate can be applied to an Al plated steel sheet in a solution state. Further, Zn hydroxide, Zn phosphate, and Zn organic acid are believed to precipitate as compounds in the baking step after application or the heating step at the time of hot stamping, but compared with a solution dispersed in water, there is no secondary aggregation in water and precipitation occurs in a finer form. Therefore, it is believed that the precipitated particles sinter and therefore the strength as a coating can be easily maintained.

(35) The surface coating layer improves the lubricity, so even with an Al plated steel sheet which is inferior in shapeability, the shapeability at the time of hot press forming can be improved. Further, it is possible to enjoy the excellent corrosion resistance of the Al plated steel sheet. Further, the excellent lubricity of the surface coating layer suppresses the adhesion of the AlFe intermetallic compounds on the die. Even if the Al plating layer powderizes, the surface coating layer which contains the Zn compound can prevent the powder (powder of AlFe intermetallic compound) from adhering to the die which is used for the later hot press forming. Accordingly, a step of removing the powder of the AlFe intermetallic compound which adheres to the die etc. become unnecessary, so the productivity of the shaped product can be further improved.

(36) Further, the surface coating layer can play the role of a protective layer which protects damage to the Al plating layer which can occur at the time of hot press forming and can improve the shapeability. Furthermore, the surface coating layer does not lower the spot weldability and coating adhesion or other aspects of performance either. If the treatment solution when forming the surface coating layer in high in water solubility, the spot weldability and coating adhesion deteriorate. If the treatment solution is high in water solubility, the applied treatment solution easily runs off from the steel sheet and the deposition ability deteriorates.

(37) Furthermore, the surface coating layer can greatly improve the coated corrosion resistance and can reduce the amount of deposition of Al of the Al plating layer compared with the past. As a result, even when rapidly performing hot press forming, adhesion can be reduced and the productivity of the shaped product is further raised.

(38) Hot Press Method

(39) Next, the method of hot pressing the steel sheet for hot press use of the present invention will be explained.

(40) In the hot press method of the present invention, first, the plated steel sheet for hot press use is blanked as required, then heated to a high temperature to make the plated steel sheet for hot press use soften. Further, the softened plated steel sheet for hot press use is press formed to shape it, then is cooled. By softening the plated steel sheet for hot press use once in this way, it is possible to easily perform the subsequent press forming. Further, the plated steel sheet for hot press use of the present invention can be hardened by heating and cooling and realize an approximately 1500 MPa or more high tensile strength.

(41) As the heating method, in addition to the usual electrical furnace, a radiant tube furnace, infrared furnace, etc. may be employed.

(42) The Al plated steel sheet melts if heated to the melting point or more and simultaneously diffuses with Fe whereby the Al phase changes to the AlFe alloy phase and AlFeSi alloy phase. The AlFe alloy phase and AlFeSi alloy phase have high melting points of 1150 C. or so. The AlFe phase and AlFeSi phase come in a plurality of types and if heated at a high temperature or heated for a long time, change to the higher Fe concentration alloy phase.

(43) The surface state which is desirable for the final shaped product is a state alloyed up to the surface and a state where the concentration of Fe in the alloy phase is not that high. If unalloyed Al remains, only this portion rapidly corrodes, the coated corrosion resistance deteriorates, and blisters occur extremely easily, so this is not desirable. On the other hand, if the concentration of Fe in the alloy phase becomes too high, the alloy phase itself falls in corrosion resistance, the coated corrosion resistance deteriorates, and blisters easily occur. That is, the corrosion resistance of the alloy phase depends on the concentration of Al in the alloy phase. Therefore, to improve the coated corrosion resistance, the state of alloying is controlled by the amount of deposition of Al and the heating conditions.

(44) In the present invention, the average temperature elevation rate in the temperature region from 50 C. to a temperature 10 C. lower than the maximum peak temperature is preferably made 10 to 300 C./sec. The average temperature elevation rate governs the productivity in press forming plated steel sheet for hot press use. If the average temperature elevation rate is less than 10 C./sec, softening of the steel sheet for hot press use requires time. On the other hand, if over 300 C., the softening is rapid, but the alloying of the plating layer becomes remarkable and causes powdering. The general average temperature elevation rate is, in the case of heating in the atmosphere, about 5 C./sec. An average temperature elevation rate of 100 C./sec or more can be achieved by ohmic heating or high frequency induction heating.

(45) The plated steel sheet for hot press use of the present invention can realize a high average temperature elevation rate, so the productivity of the shaped product can be improved. Further, the average temperature elevation rate has an effect on the chemical composition and thickness of the AlFe alloy phase, so is one of the important factors in control of the quality in plated steel sheet for hot press use. In the case of the plated steel sheet for hot press use of the present invention, the temperature elevation rate can be raised to 300 C./sec, so a broader range of control of quality becomes possible.

(46) Regarding the maximum peak temperature, due to the principle of the hot press method, heating is necessary in the austenite region, so usually a temperature of 900 to 950 C. or so is employed. In the hot press method of the present invention, the maximum peak temperature is not particularly limited, but if less than 850 C., sufficient quenching hardness is not obtained, so this is not preferable. Further, the Al plating layer has to be made an AlFe alloy phase. From this viewpoint, it is not preferable to make the maximum peak temperature less than 850 C. On the other hand, if the maximum peak temperature exceeds 1000 C., the alloying will proceed too far, the concentration of Fe in the AlFe alloy phases will rise, and a drop in the coated corrosion resistance will be invited. The upper limit of the maximum peak temperature cannot be defined across the board since it depends also on the temperature elevation rate and amount of deposition of Al, but even if considering economy, it is not preferable to make the maximum peak temperature is 1100 C. or more.

(47) Advantageous Effects of Plated Steel Sheet for Hot Press Use and Hot Press Method of Present Invention

(48) The plated steel sheet for hot press use of the present invention has a surface coating layer which contains a compound which contains Zn, in particular which contains Zn hydroxide, so a high lubricity is realized and the chemical convertability is improved. Further, the plated steel sheet for hot press use of the present invention is resistant to peeling of the coating after shaping. As a result, adhesion of the AlFe intermetallic compounds to the die is prevented, the shapeability and productivity at the time of hot press forming are improved, and the chemical convertability after hot press forming is also improved. Furthermore, the steel sheet for hot press use of the present invention is excellent in adhesion of the Al plating layer and surface coating layer after shaping and also excellent in corrosion resistance of the shaped product, that is, the coated corrosion resistance.

(49) The reason the chemically converted coating forms due to a Zn compound such as Zn hydroxide is unclear at the present stage, but the chemical conversion reaction proceeds while triggering an etching reaction by acid of the material. The surface of the AlFe intermetallic compound is extremely inert to acid, so it is guessed that the reaction has difficulty proceeding. A Zn compound is an amphoteric compound and dissolves in an acid, so is believed to react with a chemical conversion solution.

EXAMPLES

(50) Next, examples will be shown while further explaining the present invention. Note that, the present invention is not limited to the examples which are shown below.

Example 1

(51) A cold rolled steel sheet of the chemical composition which is shown in Table 1 (sheet thickness 1.4 mm) was used. This cold rolled steel sheet was plated with Al by the Sendzimir process. The annealing temperature was made about 800 C., the Al plating bath contained Si: 9%, and Fe which was eluted from the cold rolled steel sheet was contained. The amount of deposition of Al after plating was adjusted by the gas wiping method to 160 g/m.sup.2 at both surfaces. After cooling, a suspension or aqueous solution which was shown in Table 2 was coated by a roll coater and was baked on at about 80 C. to produce a test material. Note that, each solution which is shown in Table 2 was obtained by using reagents and mixing them with distilled water to form a suspension or aqueous solution.

(52) The characteristics of the thus produced test material were evaluated by the following methods. Note that, the average temperature elevation rate when heating to 900 C. was made 5 C./sec.

(53) (1) Hot Lubricity

(54) The apparatus which is shown in FIG. 1 was used to evaluate the hot lubricity. A 150200 mm test material was heated to 900 C., then a steel ball was pushed against it from the top at 700 C. to measure the push-in load and pull-out load. The (pull-out load)/(push-in load) was made the dynamic coefficient of friction.

(55) (2) Coating Adhesion

(56) The test material was inserted into an atmosphere furnace, heated at 900 C. for 6 minutes, taken out, then immediately clamped in a stainless steel die and rapidly cooled. The cooling rate at this time was made 150 C./sec. Next, the test material was cut to 5050 mm and used for a wrapping test. The method was to run gauze to which 2.0 kgf (1 kgf is 9.8N) of load was applied back and forth 10 times over a 30 mm length, measure the amount of deposition of Zn before and after the test, and calculate the amount of reduction %.

(57) (3) Spot Weldability

(58) The test material was inserted into an atmosphere furnace, heated at 900 C. for 6 minutes, taken out, then immediately clamped in a stainless steel die and rapidly cooled. The cooling rate at this time was made 150 C./sec. Next, the test material was cut to 3050 mm and the range of suitable current for spot welding (difference of upper limit current and lower limit current) was measured. The measurement conditions were as follows: The lower limit current was made the current value when the nugget size 4t.sup.1/2 (t: sheet thickness) was 4.4 mm, while the upper limit current was made the dust generating current.
Electrode: made of chromium copper, DR type (tip size 6 mm, 40R radius shape)
Applied voltage: 400 kgf (1 kgf is 9.8N)
Electrification time: 12 cycles (60 Hz)

(59) (4) Coated Corrosion Resistance

(60) The test material was inserted into an atmosphere furnace, heated at 900 C. for 6 minutes, taken out, then immediately clamped in a stainless steel die and rapidly cooled. The cooling rate at this time was made 150 C./sec. Next, the test material was cut to 70 150 mm and was chemically converted using a chemical conversion solution (PB-SX35) made by Japan Parkerizing, then was given an electrodeposition coating (Powernix 110) made by Nippon Paint and was baked at 170 C. to form a 20 m coating.

(61) The coated corrosion resistance was evaluated based on the JASO M609 of the Society of Automotive Engineers of Japan. The coating was cross-cut by a cutter in advance and the width of blisters from the cross-cuts after an 180 cycle (60 day) corrosion test (maximum value of one side) were measured. The reference material was a general corrosion-proof steel sheet comprised of hot dip galvannealed steel sheet with zinc deposited to 45 g/m.sup.2 per surface. If the coated corrosion resistance is better than the reference material, use as corrosion-proof steel sheet is possible. Note that the width of the blisters of the reference material was 7 mm.

(62) TABLE-US-00001 TABLE 1 Chemical Composition of Test Material (mass %) C Si Mn P S Ti B Al 0.22 0.12 1.25 0.01 0.005 0.02 0.003 0.04

(63) TABLE-US-00002 TABLE 2 Compound A B C D E F G H Coating Zn(OH).sub.2 Zn.sub.3(PO.sub.4).sub.2 Zn(C.sub.17H.sub.33COO).sub.2 Zn(CH.sub.3COO).sub.2 C.sub.12H.sub.220.sub.14Zn3H.sub.2O ZnO ZnSO.sub.4 Zn(NO.sub.3).sub.2 treatment Suspension Suspension Suspension Aqueous Suspension Suspension Aqueous Aqueous solution solution solution solution Concentration 200 200 200 200 200 200 200 200 (g/l) *1 Zn deposition 1 g/m.sup.2 1 g/m.sup.2 1 g/m.sup.2 1 g/m.sup.2 1 g/m.sup.2 1 g/m.sup.2 1 g/m.sup.2 1 g/m.sup.2 am't *2 *1 Inclusion, by mass %, of 20% of urethane resin with respect to Zn compounds in addition to Zn compounds. *2 Amount when all Zn.

(64) TABLE-US-00003 TABLE 3 Hot Coating Spot Coated lubric- ad- weld- corrosion No. Compound ity hesion ability resistance Remarks 1 A 0.74 8% 2.1 kA 1.8 mm Inv. ex. 2 B 0.74 9% 2.2 kA 2.2 mm Inv. ex. 3 C 0.75 7% 2.0 kA 2.3 mm Inv. ex. 4 D 0.76 5% 2.2 kA 2.1 mm Inv. ex. 5 E 0.79 9% 2.0 kA 2.4 mm Inv. ex. 6 F 0.75 25% 2.0 kA 2.0 mm Comp. ex. 7 Untreated 0.95 2.1 kA 6.0 mm Conv. ex. 8 A + 5% G 0.76 9% 2.0 kA 2.2 mm Inv. ex. 9 A + D 0.73 10% 2.2 kA 2.1 mm Inv. ex. 10 A + 5% H 0.77 10% 2.0 kA 2.5 mm Inv. ex. 11 G 0.92 20% 1.4 kA 4.5 mm Comp. ex. 12 H 0.77 23% 1.5 kA 5.2 mm Comp. ex. 13 A + 10% G 0.77 11% 1.9 kA 2.4 mm Inv. ex. 14 A + 10% G 0.78 11% 1.8 kA 2.7 mm Inv. ex. 15 A + 15% G 0.81 14% 0.9 kA 3.5 mm Comp. ex. 16 A + 15% H 0.82 14% 0.8 kA 4.1 mm Comp. ex. Note 1) A + D indicates inclusion of A and D in equal amounts. The amount of deposition of the surface coating was made 1 g/m.sup.2 by total amount of Zn. Note 2) A + 5 to 15% G indicates inclusion of G in 5 to 15% by mass % with respect to A. The amount of deposition of the surface coating was made 1 g/m.sup.2 by total amount of Zn. Note 3) A + 5 to 15% H indicates inclusion of H in 5 to 15% by mass % with respect to A. The amount of deposition of the surface coating was made 1 g/m.sup.2 by total amount of Zn.

(65) The results of evaluation are shown in Table 3. The hot lubricity is shown by the measured dynamic coefficient of friction, the coating adhesion is shown by the amount of reduction of Zn % before and after heating, the spot weldability is shown by the suitable range of current, and the coated corrosion resistance is shown by the width of blisters. Note that, No. 7 was Al plated steel sheet as is without formation of a surface coating layer.

(66) From Table 3, it was confirmed that by forming surface coating layers which contain Zn compounds of A to E, it is possible to improve the hot lubricity, coating adhesion, and coated corrosion resistance without causing the deterioration of the spot weldability.

(67) Here, No. 6 is a comparative example where a treatment solution comprising a suspension of ZnO and a urethane-based binder mixed together is coated. While the hot lubricity and coated corrosion resistance were excellent, the coating adhesion was 25% or remarkably inferior compared with the invention examples.

(68) Further, the comparative examples where surface coating layers which contain Zn compounds of G and H are formed (Nos. 11 and 12) were inferior in coating adhesion and spot weldability. This is because the treatment solutions which contain the compounds G and H are high in water solubility, easily run off when coated on Al plated steel sheet, and are inferior in deposition ability. However, as shown in Nos. 8 and 10, if the contents in the surface coating layers of G and H are, by mass %, 10% or less, it was confirmed that the effect on deterioration of the coating adhesion and spot weldability was small.

(69) Next, to what extent a surface coating which contains a Zn compound should be formed was determined by changing the amount of deposition of surface coating layer and evaluating the hot lubricity. The amount of deposition of the surface coating was evaluated by the amount of deposition of Zn in the surface coating. The treatment solution used was one which contained the Zn compound of A of Table 2. The results are shown in FIG. 2.

(70) As clear from FIG. 2, it was confirmed that by an amount of deposition of Zn of 0.5 g/m.sup.2 or more, more preferably 1 g/m.sup.2 or more, the hot lubricity can be improved. The various values in FIG. 2 are shown in Table 4. As clear from Table 4, it was confirmed that by an amount of deposition of Zn of 2 g/m.sup.2, the value of the coefficient of hot friction became saturated.

(71) TABLE-US-00004 TABLE 4 Coefficient of Hot Friction Am't of 0 0.4 0.7 1.1 1.5 2 2.4 2.9 5 7 deposition (g/m.sup.2) Coefficient of 0.95 0.84 0.76 0.71 0.65 0.65 0.66 0.64 0.61 0.6 hot friction

Example 2

(72) A treatment solution was prepared by changing the ratio of addition (%) of a urethane resin to a suspension which contains the Zn compound of A of Table 2 with respect to the Zn(OH).sub.2. This was applied to the Al plated steel sheet of Example 1 to form a surface coating layer and prepare a test material. The baking conditions were the same as in Example 1. Further, the adhesion of this test material was evaluated. The methods of evaluation were the same as Example 1 except for the evaluations being performed before the heating. That is, the test material was cut to 5050 mm and subjected to a wrapping test. The method was to run gauze to which 1.5 kgf (1 kgf is 9.8N) of load was applied back and forth 10 times over a 30 mm length, measure the amount of deposition of Zn before and after the test, and calculate the amount of reduction %.

(73) TABLE-US-00005 TABLE 5 Table 5. Coating Adhesion Before Heating Resin ratio 0% 5% 9% 16% 28% 50% Adhesion before 20% 5% 1% 0.2% 0.2% 0.2% heating

(74) The results are shown in Table 5. It could be confirmed that the adhesion before heating was improved by the addition of urethane resin. Further, it could be confirmed that even if adding urethane resin in 16% or more, the effect became saturated.

Example 3

(75) A steel sheet for hot press use of the present invention which was formed using a treatment solution which contains the Zn compound of No. 1 in Example 1 was used. An infrared ray furnace was used to heat the steel sheet by an average heating rate of 30 C./second to evaluate the characteristics of the test material. The methods of evaluation were similar to the methods which were shown in Example 1 except for the heating method. The results of evaluation are shown in Table 6. The coated corrosion resistance was superior to the case of No. 1 as a result. It could be confirmed that the rapid heating method was effective.

(76) TABLE-US-00006 TABLE 6 Results of Evaluation at Time of Application of Rapid Heating Hot Coating Spot Coated corrosion Compound lubricity adhesion weldability resistance A 0.75 7% 2.0 kA 0.9 mm

Example 4

(77) A cold rolled steel sheet of the chemical composition which is shown in Table 1 (sheet thickness 1.4 mm) was used. This cold rolled steel sheet was plated with Al by the Sendzimir process. The Al plating bath was changed in Si concentration to 3, 6, 9, 13, 15, 18, and 21%. In addition, it contained Fe which was eluted from the cold rolled steel sheet. The amount of deposition of Al after plating was adjusted by the gas wiping method to 160 g/m.sup.2 at both surfaces. After cooling, a treatment solution which contained the Zn compound which was shown by A in Table 2 was coated by a roll coater and was baked on at about 80 C. to produce test materials. These test materials were evaluated for characteristics by methods similar to Example 1. Note that, the amount of deposition of Zn was in each case about 1 g/m.sup.2. The results of evaluation are shown in Table 7. As clear from Table 7, it could be considered that when the Si concentration is 3 to 15%, the coated corrosion resistance is particularly excellent.

(78) TABLE-US-00007 TABLE 7 Si Coated concentration Hot Coating Spot corrosion (mass %) lubricity adhesion weldability resistance 3 0.74 13% 2.2 kA 2.2 mm 6 0.73 10% 2.1 kA 1.9 mm 9 0.74 9% 2.1 kA 1.8 mm 13 0.73 9% 2.1 kA 1.8 mm 15 0.74 9% 2.0 kA 1.7 mm 18 0.73 12% 2.0 kA 2.3 mm 21 0.74 13% 1.9 kA 2.3 mm

(79) As explained above, while preferred embodiments of the present invention were explained in detail, the present invention is not limited to these embodiments. Any embodiments which are within the scope described in the claims shall be considered to be included in the present invention.

INDUSTRIAL APPLICABILITY

(80) According to the present invention, when hot pressing the Al plated steel sheet, since the lubricity is good and the workability is improved, a more complicated shape of shaped product than the past can be press formed. Furthermore, labor can be saved in the maintenance and inspection of the hot press die and the productivity of the shaped product can be improved. The shaped product after hot press forming as well is good in chemical convertability, so the painting ability and corrosion resistance of the final shaped product can be improved as well. In this way, the present invention enables hot pressing of Al plated steel sheet to be expanded to the automobile industry etc. Therefore, the present invention is high in value of application in industry.