This disclosure relates to a hot press forming part and a method of manufacturing the same. The disclosure particularly relates to a method for manufacturing a hot press forming part from a coated steel sheet wherein, while press forming the coated steel sheet heated beforehand into a predetermined shape, the steel sheet is simultaneously quenched to attain a predetermined strength (such that the tensile strength is at least 1180 MPa grade), and a hot press forming part manufactured by the same.
In recent years, strengthening and sheet metal thinning of automotive parts have been required. As the thin steel sheets (hereinafter referred to as “steel sheets”) used have higher strength, press formability is deteriorated, and forming the steel sheets into the desired part shape is more difficult.
The following technique is known to solve this problem: while hot press forming a blank sheet heated to high temperature into a desired shape using a tool of press forming, the steel sheet is quenched in the die by heat extraction, thus enhancing the hardness of the hot press formed part.
For example, GB1490535A (PTL 1) proposes a technique in which, when manufacturing a part of a predetermined shape by hot pressing a blank sheet (steel sheet) heated to an austenite single phase region of about 900° C., the blank sheet is quenched in a tool of press forming simultaneously with the hot press forming, thus enhancing the strength of the part.
However, the technique proposed in PTL 1 has a problem in that, when heating the steel sheet to high temperature of about 900° C. before the pressing, oxide scale (iron oxide) forms on the surface of the steel sheet, and the oxide scale peels during the hot press forming and damages the die or the surface of the hot press formed part. Besides, the oxide scale remaining on the surface of the part causes poor appearance and lower coating adhesion. Accordingly, the oxide scale on the surface of the part is typically removed by a process such as pickling or shot blasting. Such a process, however, causes lower productivity. Furthermore, while suspension parts of vehicles, automotive body parts, and the like are also required to have excellent corrosion resistance, the corrosion resistance of the hot press formed part by the technique proposed in PTL 1 is insufficient because a rust preventive film such as a coating layer is not provided on the blank sheet.
For these reasons, there is demand for hot press forming techniques that can suppress the generation of oxide scale during heating before hot press forming and also improve the corrosion resistance of the hot press formed part. To meet this demand, coated steel sheets having films such as coating layers on their surfaces, hot press forming methods using coated steel sheets, etc. are proposed.
For example, JP2001353548A (PTL 2) proposes a technique in which a steel sheet coated with Zn or a zinc-based alloy is heated to 700° C. to 1200° C. and then hot press formed to obtain a hot press formed part having a Zn—Fe-based compound or a Zn—Fe—Al-based compound on its surface. PTL 2 describes that the use of the steel sheet coated with Zn or a Zn-based alloy suppresses the oxidation of the surface of the steel sheet during heating before hot press forming, and also enables a hot press formed part having excellent corrosion resistance to be obtained.
With the technique proposed in PTL 2, the generation of oxide scale on the surface of the hot press formed part is suppressed to some extent. However. Zn in the coating layer may cause liquid metal embrittlement cracking, resulting in cracks of about 100 μm in depth in the surface layer part of the hot press formed part. Such cracks pose various problems such as a decrease in fatigue characteristics of the hot press formed part.
In view of this problem, JP201391099A (PTL 3) proposes a method in which a coated steel sheet obtained by providing a Zn—Fe-based coating layer on a surface of a steel sheet is heated to a temperature not less than Ac1 transformation temperature of the steel sheet and not more than 950° C. and then cooled to a temperature not more than the freezing point of the coating layer, before starting the forming. PTL 3 describes that liquid metal embrittlement cracking can be suppressed by starting the forming after the coated steel sheet is cooled to the temperature not more than the freezing point of the coating layer.
It is believed that the technique proposed in PTL 3 can suppress liquid metal embrittlement cracking, i.e., cracks in the surface of the hot press formed part, which are about 100 μm in depth from the interface between the coating layer and the steel toward the inside of the steel and in which Zn is detected from its interface (such cracks referred to hereinafter as “macro-cracks”). For suppressing such macro-cracks, we studied the use of Zn—Ni alloy coating obtained by blending Zn with about 9% to 25% of Ni as a coating layer with high fusing point. The γ-phase in the phase equilibrium diagram of Zn—Ni alloy has a fusing point of 860° C. or higher, which is very high as compared to that a normal Zn or Zn alloy coated layer, making it possible to suppress macro-cracks under normal press conditions.
However, in addition to the macro-cracks, minute cracking which is about 30 μm or less in depth from the interface between the coating layer and the steel toward the inside of the steel and in which Zn is not detected from its interface may also occur in the surface of the hot press formed part. Such minute cracking is called “micro-cracks”. Micro-cracks pass through the interface between the coating layer and the steel and reach the inside of the steel (steel sheet), adversely affecting the characteristics (fatigue characteristics, etc.) of the hot press formed part.
Macro-cracks also occur in, for example, a shoulder area of die R on the punch-contacting side which is subjected to only tensile strain while press forming of a hat-shaped section part (also referred to hereinafter as a “hat-shaped part”). On the other hand, micro-cracks do not occur in such area, but on the die-contacting side of side wall portions, which are subjected to compression (due to bending) followed by tensile strain (due to bend restoration). It is thus estimated that macro-cracks and micro-cracks are produced by different mechanism.
PTL 3 may suppress the occurrence of macro-cracks in a coated steel sheet having a Zn—Fe-based coating layer formed thereon, but is not necessarily effective for suppressing the occurrence of micro-cracks, because it does not consider potential micro-cracks occurring in a coated steel sheet having a Zn—Ni coating layer formed thereon.
Additionally, PTL 3 teaches that the coated steel sheet is press formed as a whole while being cooled to a temperature at or below the freezing point of the coating layer, without specifying the lowest temperature at which the press forming is started, leading to the problem of lower forming temperature resulting in higher strength of the steel sheet during press forming, and deteriorating the shape fixability (which is a characteristic that maintains the shape at press bottom dead center even after die release, because of little springback and the like).
It could thus be helpful to provide a method for, when manufacturing a hot press formed part by hot pressing a coated steel sheet having a Zn—Ni-based coating layer formed thereon, manufacturing a hot press forming part while preventing a reduction in the shape fixability during hot press forming and suppressing the occurrence of micro-cracks, and a hot press forming part manufactured by the same.
We studied means for suppressing micro-cracks (minute cracking) caused when hot press forming a Zn-based coated steel sheet.
Although the micro-crack occurrence mechanism is still unclear, press forming the Zn-based coated steel sheet at high temperature may induce minute cracking in the surface of the coated steel sheet, and such minute cracking also occurs in Zn—Ni coating. The minute cracking has a depth of about 30 μm from the interface between the coating layer and the steel (steel sheet), and passes through the interface between the coating layer and the steel (steel sheet) and reaches the inside of the steel sheet. As a result of making various research on this problem, we discovered that micro-cracks are suppressed by performing hot press forming at low temperature. Further, the effect of significantly reducing the amount of coating attached to the tool of press forming, which would be quite large to cause problems with conventional coated steel sheets for hot press forming, was obtained by setting a low temperature for press forming as mentioned above.
However, when the press forming temperature is lower, the strength of the steel sheet is higher, and accordingly the shape fixability is lower. Thus, the advantages of the hot press forming cannot be exploited.
We then conceived cooling, before performing hot press forming, only those portions of the steel sheet that are processed such that micro-cracks would occur during the press process. Then we made further research on the influence of strain during forming on the occurrence of micro-cracks, and discovered that micro-cracks are not caused by compressive deformation or bending deformation alone, but are caused at those portions when being subjected to bending-bend restoration deformation resulting from the portions being bent and stretched afterwards.
A portion of the formed part, called a side wall portion, principally undergoes such bending-bend restoration deformation.
In draw forming, side wall portions are formed by those portions squeezed between the die and the blank holder prior to press forming. We further investigated the way of effectively cooling only such portions. As a result, it was discovered that it is possible to suppress defects in shape accuracy and to suppress the occurrence of micro-cracks in the side wall portions by, prior to press forming, squeezing the steel sheet between the die and the blank holder and, through heat extraction at the tool of press forming, cooling the steel sheet continuously (for 0.5 seconds to 3 seconds) until the temperature of the portions at which the steel sheet is squeezed between the die and the blank holder reaches 550° C. or lower and 400° C. or higher.
The exact mechanism behind this phenomenon in which cooling in the die and blank the holder prevented lowering shape accuracy is unclear, yet the reason may be as stated below.
For hat-shaped parts, typical defects in shape accuracy include angle change such that the angle formed by two faces across the bending ridgeline becomes large relative to the die angle, and wall camber such that the planes of the side wall portions have curvature. Both of these defects occur due to the difference of any stress distribution in the sheet thickness direction, and the higher the flow stress of the steel sheet during forming, the shape accuracy decreases. In other words, in hot pressing, as the forming temperature becomes lower, the flow stress increases during forming of the steel sheet, and the shape accuracy decreases. In this respect, by performing cooling in the tool of press forming as described above, the aforementioned angle change becomes small, because the portion of the steel sheet in contact with the punch shoulder portion at the time of press forming is not cooled during the cooling process in the die and the blank holder, and this portion is processed under high-temperature conditions. It is also believed that the side wall portions are reduced in shape accuracy since the temperature of the steel sheet during processing is decreased by cooling in the die and the blank holder. However, almost no deterioration of shape accuracy was observed over a holding time (within three seconds) when the temperature of the steel sheet is 400° C. or higher. The reason may be that at a steel plate temperature of 400° C. or higher (over a holding time of 3 seconds or less), the metallographic structure during the press forming was still austenite, and the stress that had been introduced during the press forming was eased by martensitic transformation after the forming process, causing no deterioration of shape accuracy. By contrast, it is considered that if the holding time exceeds 3 seconds, the metallographic structure will have already been transformed to martensite at the time of press forming, and wall camber will be caused by the stress introduced during the press forming.
The disclosure is based on the aforementioned discoveries. We thus provide the following.
[1] A method for manufacturing a hot press forming part by hot pressing, using a tool of press forming, a coated steel sheet that is obtained by forming a Zn—Ni coating layer on a surface of a steel sheet, the tool of press forming having a die, a blank holder, and a punch, the method comprising:
cooling edges of the coated steel sheet heated to a temperature range of Ac3 transformation temperature to 1000° C., with the edges squeezed between the die and the blank holder, to a temperature of 550° C. or lower and 400° C. or higher at a cooling rate of 100° C./s or higher;
performing press forming so that the press forming is started when the edges reach a temperature of 550° C. or lower and 400° C. or higher; and
after the press forming, quenching a formed body with the formed body held at the press bottom dead center while being squeezed by the tool of press forming.
[2] The method for manufacturing a hot press forming part according to [1] above, wherein the cooling and the press forming are performed while slidably moving the die with the coated steel sheet so that slidable movement is temporarily stopped before the coated steel sheet is brought into contact with the punch, or so that slidable movement before the coated steel sheet coming into contact with the punch is slower than slidable movement during press forming after the coated steel sheet coming into contact with the punch.
[3] The method for manufacturing a hot press forming part according to [1] or [2], wherein in the press forming, the blank holder is detached from the coated steel sheet to perform crush forming without using the blank holder.
[4] The method for manufacturing a hot press forming part according to [1] or [2], wherein in the press forming, draw forming is performed with the coated steel sheet squeezed between the die and the blank holder.
[5] The method for manufacturing a hot press forming part according to any one of [1] to [4], wherein the Zn—Ni coating layer contains Ni in an amount of 9 mass % or more and 25 mass % or less.
A hot press forming part manufactured by the method as recited in any one of [1] to [5].
According to this disclosure, micro-cracks do not occur, and it is possible to manufacture a hot press forming part with sufficient strength and hardness as well as satisfactory shape fixability, without causing a significant increase in load of press forming.
In the accompanying drawings:
The method for manufacturing a hot press forming part according to one of the disclosed embodiments manufactures a hot press forming part by hot pressing, using a tool of press forming, a coated steel sheet that is obtained by forming a Zn—Ni coating layer on a surface of a steel sheet, the tool of press forming having a die, a blank holder, and a punch, the method comprising, as illustrated in
The following describes the details of the blank material of the hot press formed part, the cooling (S1), the press forming (S2), and the quenching (S3).
<Blank Material of Hot Press Formed Part>
A coated steel sheet obtained by providing a Zn—Ni coating layer on a surface of the steel sheet is used as the blank material of a hot press formed part. The provision of the Zn—Ni coating layer on the surface of the steel sheet ensures the corrosion resistance of the hot press formed part.
The method of forming the Zn—Ni coating layer on the surface of the steel sheet is not particularly limited, and may be any of the methods such as hot-dip galvanizing and electro-galvanizing. The coating weight per side is preferably 10 g/m2 or more and 90 g/m2 or less.
The Ni content in the coating layer is preferably 9 mass % or more and 25 mass % or less. In the case of forming the Zn—Ni coating layer on the surface of the steel sheet by electro-galvanizing, a γ phase having any of the crystal structures of Ni2Zn11, NiZn3, and Ni5Zn21 is formed when the Ni content in the coating layer is 9 mass % or more and 25 mass % or less. The γ phase has a high fusing point, and thus is advantageous in preventing the coating layer from evaporating when heating the coated steel sheet before hot press forming. The γ phase is also advantageous in suppressing liquid metal embrittlement cracking during high-temperature hot press forming.
The coated steel sheet 1 is heated to a temperature range of Ac3 transformation temperature to 1000° C. If the heating temperature of the coated steel sheet 1 is below Ac3 transformation temperature, a sufficient amount of austenite cannot be obtained during heating, leading to the presence of ferrite during press forming. As a result, sufficient strength and good shape fixability are difficult to achieve through hot press forming. When the heating temperature of the coated steel sheet 1 exceeds 1000° C., on the other hand, the coating layer evaporates or excessive oxide generation occurs in the surface layer part, as a result of which the resistance to oxidation declines or the corrosion resistance of the hot press formed part declines. Therefore, the heating temperature is from Ac3 transformation temperature to 1000° C. Preferably, the heating temperature is from Ac3 transformation temperature+30° C. to 950° C. The method of heating the coated steel sheet 1 is not particularly limited, and may be any of the methods such as heating in an electric furnace, an induction heating furnace, and a direct current furnace. Although not particularly limited, the thickness of the steel sheet is preferably 0.8 mm to 4.0 mm from the perspective of guaranteeing the rigidity of the press formed part and ensuring the cooling rate during cooling in the tool of press forming. More preferably, the thickness is 1.0 mm 3.0 mm.
<Cooling (S1) and Press Forming (S2)>
In the cooling (S1), edges of the coated steel sheet thus heated are cooled, with the edges being squeezed between the die and the blank holder, to a temperature of 550° C. or lower and 400° C. or higher at a cooling rate of 100° C./s or higher.
Additionally, in the press forming (S2), press forming is performed so that the press forming is started when the edges of the coated steel sheet reach a temperature of 550° C. or lower and 400° C. or higher.
It is noted here that in the cooling (S1), the temperature at start of cooling, with the edges of the heated coated steel sheet 1 squeezed between the die and the blank holder, is preferably 800° C. or lower from the perspective of preventing the risk of the Zn—Ni coating layer being adhered to the tool of press forming, and preferably 670° C. or higher from the perspective of guaranteeing the strength after hot press forming.
As used herein, the edges refer to those portions of the coated steel sheet that form, after subjection to the press forming, flange portions with at least the lower portions (on the flange side) of the side wall portions of a formed body. For example, when a hat-shaped section part as illustrated in
In addition, cooling in the tool of press forming using the die and the blank holder is adopted because, for example, when a hat-shaped section part is formed, the edges of the steel sheet that are squeezed between the die and the blank holder will be rapidly cooled, while other portions of the steel sheet that are in contact with the shoulder areas of the punch during the press forming will hardly be cooled, and thus can be press formed while being kept at high temperature.
Moreover, the cooling rate for cooling in the tool of press forming is set to 100° C./s or higher because, when a forming part is press formed into a hat-shaped part, for example, this cooling rate enables the side wall portions (portions squeezed by the tool of press forming) of the press formed body to have a martensite single phase structure, and thus allows for strengthening, without increasing cost, of the side wall portions.
In the following, this will be described in detail.
On the other hand, if the press forming start temperature is low as shown in graph (b) of
Thus, simply lowering of the press forming start temperature results in graph (b) of
Normally, the upper limit of the cooling rate for cooling in the tool of press forming is about 500° C./s.
In the cooling step, the edges are cooled to 550° C. or lower because, above 550° C., cooling becomes insufficient, causing micro-cracks after subjection to the hot press forming. In addition, the lower limit of the cooling temperature is 400° C. because, if the edges are cooled below 400° C., the coated steel sheet 1 will be excessively cooled before subjection to the press forming, leading to deterioration in shape fixability.
We conducted experiments to examine the relationship between cooling temperature, occurrence of micro-cracks, and shape fixability in the cooling step, and the results thereof will be described below.
As the blank material, a Zn—Ni coated steel sheet having a sheet thickness of 1.6 mm that was prepared by applying Zn-12% Ni coating to both surfaces thereof with a coating weight per side of 60 g/m2 was used. The heating temperature was 900° C., the temperature at start of cooling in the tool of press forming was about 700° C., the blank holding force (BHF) was 98 kN, and the bottom dead center holding time was 15 s.
In the cooling step, cooling in the tool of press forming was controlled by the time for which the blank material was held by the die 3 and the blank holder 5 before the start of press forming. Specifically, in conventional press forming as illustrated in
For the change in temperature of a steel sheet, as indicated by steel sheet 9 in
The change in temperature of the edge of the steel sheet caused by cooling in the tool of press forming is, as illustrated in
For evaluation, observations were made to: (i) determine the presence of micro-cracks by observing the cross sections of the side wall portions of the press forming part; (ii) determine the hardness of the press forming part; (iii) determine the load of press forming; and (iv) determine the shape fixability by measuring the amount of mouth opening deformation of the hat-like opening of the press forming part (the difference between the width dimension of the opening after die release following the press forming and the width of the press forming part conformed to the tool of press forming).
As described above, in the cooling step, by cooling the edges of the heated coated steel sheet, with the edges squeezed between the die and the blank holder, to a temperature of 550° C. or lower to 400° C. or higher at a cooling rate of 100° C./s or higher before the start of press forming, it becomes possible for the press forming part to have a sufficient strength, and it becomes possible to prevent the occurrence of micro-cracks, prevent an increase in the load of press forming, and achieve satisfactory shape fixability.
While the method for cooling the coated steel sheet 1 in the tool of press forming prior to press forming is not particularly limited, as mentioned above, cooling with the blank holder 5 is preferable because it facilitates controlling surface temperature.
In
Further, the press forming start temperature at which the press forming is started is normally controlled by the cooling time. For example, the relation between the time of cooling in the tool of press forming and the decrease in blank temperature is measured beforehand, and based on this relation, the press forming start temperature is controlled. It is also possible to dispose temperature measuring elements such as a thermocouple on the surface of the tool of press forming to directly measure the temperature of the coated steel sheet 1 and control the press forming start temperature.
Further, in order to suppress the rise in temperature of the tool of press forming during continuous press forming and reduce the variation in the cooling rate, it is also possible to perform cooling of the tool of press forming by disposing water cooling piping in the die 3 or the blank holder 5, or to use material with high thermal conductivity for the surface of the die 3 or the blank holder 5.
As shown in
Further, as shown in
While
Although the press forming machine to be used is not particularly limited, when the slidable movement speed is changed in
Further, the press forming method is not particularly limited either. Possible methods include draw forming where forming is performed with the coated steel sheet 1 squeezed between the die 3 and the blank holder 5 as shown in
<Quenching (S3)>
In the quenching (S3), a formed body 1′ after the press forming is quenched with the formed body 1′ held at the press bottom dead center while being squeezed by the tool of press forming. In order to quench the formed body after press forming, the slidable movement is stopped at the press bottom dead center after press forming. Although the stop time i.e. the holding time at the press bottom dead center differs depending on the amount of heat extraction by the tool of press forming, it is preferably 3 seconds or more. Further, although the upper limit is not particularly limited, it is preferably 20 seconds or less from the perspective of productivity.
In order to hold the formed body in the tool of press forming for a certain period of time to obtain a quenched structure, for example, a hot rolled steel sheet or cold rolled steel sheet having a chemical composition that includes (consists of), in mass %, C: 0.15% or more and 0.50% or less, Si: 0.05% or more and 2.00% or less, Mn: 0.50% or more and 3.00% or less, P: 0.10% or less, S: 0.050% or less, Al: 0.10% or less and N: 0.010% or less, with the balance including Fe and inevitable impurities is preferably used as the steel sheet. The reasons of limitation of each component are given below. Here, “%” indicating the content of each component is “mass %”, unless otherwise stated.
C: 0.15% or More and 0.50% or Less
C is an element that improves the strength of steel. To enhance the strength of the hot pressed part, the C content is preferably 0.15% or more. When the C content exceeds 0.50%, on the other hand, the weldability of the hot press formed part and the blanking workability of the raw material (steel sheet) decrease significantly. Accordingly, the C content is preferably 0.15% or more and 0.50% or less, and more preferably 0.20% or more and 0.40% or less.
Si: 0.05% or More and 2.00% or Less
Si is an element that improves the strength of steel, as with C. To enhance the strength of the hot pressed part, the Si content is preferably 0.05% or more. When the Si content exceeds 2.00%, on the other hand, a surface defect called red scale increases significantly during hot rolling when manufacturing the steel sheet. Accordingly, the Si content is preferably 0.05% or more and 2.00% or less, and more preferably 0.10% or more and 1.50% or less.
Mn: 0.50% or More and 3.00% or Less
Mn is an element that enhances the quench hardenability of steel, and is effective in suppressing the ferrite transformation of the steel sheet and improving quench hardenability in the cooling process after the hot press forming. Mn also has a function of decreasing the Ac3 transformation temperature, and so is an element effective in lowering the heating temperature of the coated steel sheet 1 before the hot pressing. To achieve these effects, the Mn content is preferably 0.50% or more. When the Mn content exceeds 3.00%, on the other hand, Mn segregates and the uniformity of the characteristics of the steel sheet and hot press formed part declines. Accordingly, the Mn content is preferably 0.50% or more and 3.00% or less, and more preferably 0.75% or more and 2.50% or less.
P: 0.10% or Less
When the P content exceeds 0.10%, P segregates to grain boundaries, and the low temperature toughness of the steel sheet and hot press formed part decreases. Accordingly, the P content is preferably 0.10% or less, and more preferably 0.01% or less. Excessively reducing P, however, leads to longer refining time and higher cost, and accordingly, P content is preferably 0.003% or more.
S: 0.050% or Less
S is an element that forms a coarse sulfide by combining with Mn and causes a decrease in ductility of steel. The S content is preferably reduced as much as possible, though up to 0.050% is allowable. Accordingly, the S content is preferably 0.050% or less, and more preferably 0.010% or less. Excessively reducing S, however, leads to longer refining time and higher cost, and accordingly, S content is preferably 0.001% or more.
Al: 0.10% or Less
When the Al content exceeds 0.10%, oxide inclusions in steel increase, and the ductility of steel declines. Accordingly, the Al content is preferably 0.10% or less, and more preferably 0.07% or less. Meanwhile, Al functions as a deoxidizer, and so the Al content is preferably 0.01% or more to improve the cleanliness of steel.
N: 0.010% or Less
When the N content exceeds 0.010%, nitrides such as AlN form in the steel sheet, which causes lower formability during hot pressing. Accordingly, the N content is preferably 0.010% or less, and more preferably 0.005% or less. Excessively reducing N, however, leads to longer refining time and higher cost, and accordingly, N content is preferably 0.001% or more.
These are the preferable basic components of the steel sheet. The steel sheet may further include the following elements when necessary.
At least one type selected from the group consisting of Cr: 0.01% or more and 0.50% or less, V: 0.01% or more and 0.50% or less, Mo: 0.01% or more and 0.50% or less, and Ni: 0.01% or more and 0.50% or less Cr, V, Mo, and Ni are each an element effective in enhancing the quench hardenability of steel. This effect is achieved when the content is 0.01% or more for each of the elements. When the content exceeds 0.50% for each of Cr, V, Mo, and Ni, however, the effect saturates and the cost increases. Accordingly, in the case where at least one type of Cr, V, Mo, and Ni is included, the content is preferably 0.01% or more and 0.50% or less, and more preferably 0.10% or more and 0.40% or less.
Ti: 0.01% or More and 0.20% or Less
Ti is effective for strengthening steel. The strengthening effect of Ti is achieved when the content is 0.01% or more. Ti within the specified range can be used to strengthen steel without any problem. When the Ti content exceeds 0.20%, however, the effect saturates and the cost increases. Accordingly, in the case where Ti is included, the content is preferably 0.01% or more and 0.20% or less, and more preferably 0.01% or more and 0.05% or less.
Nb: 0.01% or More and 0.10% or Less
Nb is also effective for strengthening steel. The strengthening effect of Nb is achieved when the content is 0.01% or more. Nb within the specified range can be used to strengthen steel without any problem. When the Nb content exceeds 0.10%, however, the effect saturates and the cost increases. Accordingly, in the case where Nb is included, the content is preferably 0.01% or more and 0.10% or less, and more preferably 0.01% or more and 0.05% or less.
B: 0.0002% or More and 0.0050% or Less
B is an element that enhances the quench hardenability of steel, and is effective in suppressing the generation of ferrite from austenite grain boundaries and obtaining a quenched structure when cooling the steel sheet after the hot press forming. This effect is achieved when the B content is 0.0002% or more. When the B content exceeds 0.0050%, however, the effect saturates and the cost increases. Accordingly, in the case where B is included, the content is preferably 0.0002% or more and 0.0050% or less, and more preferably 0.0005% or more and 0.0030% or less.
Sb: 0.003% or More and 0.030% or Less
Sb has an effect of suppressing a decarburized layer generated in the surface layer part of the steel sheet from when a steel sheet is heated before the hot press forming to when the steel sheet is cooled by the process of hot press forming. To achieve this effect, the Sb content is preferably 0.003% or more. When the Sb content exceeds 0.030%, however, the rolling load increases during steel sheet manufacture, which may cause lower productivity. Accordingly, in the case where Sb is included, the content is preferably 0.003% or more and 0.030% or less, and more preferably 0.005% or more and 0.010% or less.
The components (balance) other than the above components are Fe and inevitable impurities.
The manufacturing condition of the coated steel sheet 1 used as the raw material of the hot press formed part is not particularly limited. The manufacturing condition of the steel sheet is not particularly limited. For example, a hot rolled steel sheet (pickled steel sheet) having a predetermined chemical composition or a cold rolled steel sheet obtained by subjecting the hot rolled sheet to cold rolling may be used as the steel sheet.
The condition when forming the Zn—Ni coating layer on the surface of the steel sheet to obtain the coated steel sheet 1 is not particularly limited. In the case where a hot rolled steel sheet (pickled steel sheet) is used as the steel sheet, the coated steel sheet 1 may be obtained by subjecting the hot rolled steel sheet (pickled steel sheet) to Zn—Ni coating treatment.
In the case where a cold rolled steel sheet is used as the steel sheet, the coated steel sheet 1 may be obtained by subjecting the cold rolled steel sheet to Zn—Ni coating treatment after cold rolling.
In the case of forming a Zn—Ni coating layer on the surface of the steel sheet, for example, the Zn—Ni coating layer may be formed by cleaning and pickling the steel sheet, and then subjecting the steel sheet to electroplating treatment with a current density of 10 A/dm2 or more and 150 A/dm2 or less in a plating bath having a pH of 1.0 or more and 3.0 or less and a bath temperature of 30° C. or more and 70° C. or less and containing: 100 g/L or more and 400 g/L or less nickel sulfate hexahydrate; and 10 g/L or more and 400 g/L or less zinc sulfate heptahydrate. In the case where a cold rolled steel sheet is used as the steel sheet, the cold rolled steel sheet may be subjected to annealing treatment before the cleaning and pickling. The Ni content in the coating layer may be set to a desired Ni content (for example, 9 mass % or more and 25 mass % or less) by appropriately adjusting the concentration of the zinc sulfate heptahydrate or the current density within the above-mentioned range. The coating weight of the Zn—Ni coating layer may be set to a desired coating weight (for example, 10 g/m2 or more and 90 g/m2 or less per side) by adjusting the current passage time.
Experiments were performed to confirm the effect of the method for manufacturing a hot press forming part described herein. These experiments will be described below.
Steels having the compositions shown in Table 1 were each smelted into a casting slab, and the casting slab was heated to 1200° C., hot rolled at a finisher delivery temperature of 870° C., and coiled at 600° C. to obtain a hot rolled steel sheet.
The hot rolled steel sheet was then pickled and cold rolled with a rolling reduction of 50%, to obtain a cold rolled steel sheet with a thickness of 1.6 mm. The Ac3 transformation temperature in Table 1 was calculated according to the following Formula (1) (see William C. Leslie, The Physical Metallurgy of Steels, translation supervised by Nariyasu Kouda, translated by Hiroshi Kumai and Tatsuhiko Noda. Maruzen Co., Ltd., 1985, p. 273).
Ac3(° C.)=910-203√[C]+44.7×[Si]−30×[Mn]+700×[P]÷400×[Al] (1)
where [C], [Si], [Mn], [P], and [Al] are the contents (mass %) in steel of the respective elements (C, Si, Mn, P, and Al).
Using the cold rolled steel sheet obtained as described above as a steel sheet, each of a pure Zn coating layer, a Zn—Fe coating layer, and a Zn—Ni coating layer was formed on the surface of the steel sheet to obtain a coated steel sheet 1. Each coating layer was formed under the following condition.
<Pure Zn Coating Layer>
The cold rolled steel sheet was passed through a continuous galvanizing line, heated to a temperature range of 800° C. or more and 900° C. or less at a heating rate of 10° C./s, and held in the temperature range for 10 s or more and 120 s or less. After this, the cold rolled steel sheet was cooled to a temperature range of 460° C. or more and 500° C. or less at a cooling rate of 15° C./s, and immersed into a galvanizing bath of 450° C. to form a Zn coating layer. The coating weight of the Zn coating layer was adjusted to a predetermined coating weight by the gas wiping method.
<Zn-Fe Coating Layer>
The cold rolled steel sheet was passed through a continuous galvanizing line, heated to a temperature range of 800° C. or more and 900° C. or less at a heating rate of 10° C./s, and held in the temperature range for 10 s or more and 120 s or less. After this, the cold rolled steel sheet was cooled to a temperature range of 460° C. or more and 500° C. or less at a cooling rate of 15° C./s, and immersed into a galvanizing bath of 450° C. to form a Zn coating layer. The coating weight of the Zn coating layer was adjusted to a predetermined coating weight by the gas wiping method. Immediately after adjusting the Zn coating layer to the predetermined coating weight by the gas wiping method, the cold rolled steel sheet was heated to 500° C. to 550° C. in an alloying furnace and held for 5 s to 60 s, to form a Zn—Fe coating layer. The Fe content in the coating layer was set to a predetermined content by changing the heating temperature in the alloying furnace or the holding time at the heating temperature within the above-mentioned range.
<Zn-Ni Coating Layer>
The cold rolled steel sheet was passed through a continuous annealing line, heated to a temperature range of 800° C. or more and 900° C. or less at a heating rate of 10° C./s, and held in the temperature range for 10 s or more and 120 s or less. After this, the cold rolled steel sheet was cooled to a temperature range of 500° C. or less at a cooling rate of 15° C./s. The cold rolled steel sheet was then cleaned and pickled, and subjected to electroplating treatment of applying current for 10 s to 100 s with a current density of 30 A/dm2 to 100 A/dm2 in a plating bath having a pH of 1.3 and a bath temperature of 50° C. and containing: 200 g/L nickel sulfate hexahydrate; and 10 g/L to 300 g/L zinc sulfate heptahydrate, thus forming a Zn—Ni coating layer. The Ni content in the coating layer was set to a predetermined content by appropriately adjusting the concentration of the zinc sulfate heptahydrate or the current density within the above-mentioned range. The coating weight of the Zn—Ni coating layer was set to a predetermined coating weight by appropriately adjusting the current passage time in the above-mentioned range.
A blank sheet of 200 mm r 400 mm was punched from each coated steel sheet 1 obtained as described above, and heated in an electric furnace having an air atmosphere. The blank sheet was set on a tool of press forming (material: SKD61), and then cooling and press forming was performed using the tool of press forming. After this, the blank sheet was quenched in the tool of press forming and released from the tool of press forming, thus manufacturing a press formed part with a hat-shaped cross section illustrated in
The type of coating layer, heating condition, cooling condition and press forming condition are shown in Table 2.
A sample was collected from the side wall portion of each obtained press formed part with a hat-shaped cross section, and the section of its surface was observed using a scanning electron microscope (SEM) with 1000 magnification for 10 fields per sample, to examine the presence or absence of micro-cracks (minute cracking in the surface of the sample, which passes through the interface between the coating layer and the steel sheet and reaches the inside of the steel sheet) and the average depth of micro-cracks. The average depth of micro-cracks was calculated by averaging the micro-crack depths of any 20 micro-cracks. The micro-crack depth mentioned here means the length (length h in
Regarding the shape accuracy of the obtained press formed part, the difference between the width W of the press forming part after die release and the width W0 of the press forming part conformed to the tool of press forming of the hat-shaped section part shown in
Furthermore, a sample for hardness measurement was collected from the side wall portion of each obtained press formed part. The hardness of the cross section of the sample was measured using a micro-Vickers hardness meter. A test was conducted with a test load of 9.8 N at 5 points in the center position in the thickness direction, and the average value thereof was used as the hardness of the samples. Here, the target hardness is 380 Hv or more.
In addition, a JIS No. 13 B tensile test piece was collected from the side wall portion of each obtained press formed part. A tensile test was conducted using the collected test piece according to JIS G 0567 (1998), to measure the tensile strength at room temperature (22±5° C.). The tensile test was conducted at a crosshead speed of 10 mm/min.
These results are also shown in Table 2.
In examples 1 to 12, the type of coating layer (Zn—Ni coating layer), cooling method (cooling in tool of press forming), cooling rate (appropriate range: 100° C./s or more), and press forming start temperature (appropriate range: 400° C. to 550° C.) are all within the range of the disclosure.
In each of the samples after pressing of examples 1 to 12, micro-cracks were not generated and the amount of mouth opening deformation was 0 mm. From these results, it can be seen that, with the press forming method described herein, it is possible to suppress the occurrence of micro-cracks while ensuring good shape fixability. Further, in all of examples 1 to 12, the hardness was 380 Hv or more, and tensile strength was 1180 MPa or more.
In comparative example 1, the type of coating layer is a Zn—Ni coating layer. However, forming was performed without performing cooling in the tool of press forming. Further, in comparative examples 2 to 4, the type of coating layer is a Zn—Ni coating layer. However, the press forming start temperatures for each of comparative examples 2 to 4 were out of the appropriate range. The press forming start temperature for comparative example 2 was 610° C. which is higher than the appropriate range, and the press forming start temperatures for comparative examples 3 and 4 were 350° C. and 230° C. which are lower than the appropriate range.
As for the samples after pressing of comparative examples 1 and 2, the amount of mouth opening deformation is 0 mm. However, micro-cracks are generated. From these results, it can be seen that, when the press forming start temperature of the steel sheet is higher than 550° C., micro-cracks are generated.
In comparative examples 3 and 4, micro-cracks are not generated. However, the amount of mouth opening deformation is 8 mm to 10 mm. From these results, it can be seen that when the cooling time is too long and the forming start temperature of the steel sheet becomes lower than 400° C., the strength of the steel sheet increases, and thus the shape fixability decreases.
In comparative examples 5 to 7, the type of coating layer is a Zn—Ni coating layer. However, the cooling method is gas cooling and the cooling rate is not 100° C./s or more. Therefore, in comparative examples 5 and 6, the press forming start temperatures of the steel sheet are out of the appropriate range (over 550° C.), and micro-cracks are generated. Further, in comparative example 7, the press forming start temperature of the steel sheet was 530° C. which is within the appropriate range. However, the amount of mouth opening deformation was 3 mm, and shape fixability was decreased. This is because, since the cooling method was gas cooling, the cooling rate was slow and the metallographic structure during the press forming was ferrite or bainite instead of an austenite single phase, and therefore the martensitic transformation after forming was decreased, and the stress introduced during the forming was hardly eased. As a result, it is believed that, angle change such that the angle formed by two faces across the bending ridgeline becomes large relative to the die angle occurred.
Further, in comparative examples 6 and 7, quenching was performed after mild cooling to a certain degree by gas cooling and pressing. Therefore, the hardness of the samples after pressing was decreased.
In comparative examples 8 and 9, the cooling method (cooling in tool of press forming), cooling rate (167° C./s, 170° C./s), and press forming start temperature (530° C. to 540° C.) are appropriate. However, the type of coating layer is different. Specifically, comparative example 8 is a coating layer of only Zn, and comparative example 9 is a coating layer of Zn—Fe, and therefore micro-cracks are generated in the samples after pressing.
Number | Date | Country | Kind |
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2014-088848 | Apr 2014 | JP | national |
2014-179073 | Sep 2014 | JP | national |
Filing Document | Filing Date | Country | Kind |
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PCT/JP2015/056439 | 2/26/2015 | WO | 00 |