WO2019180852A1 - ホットスタンプ成形体 - Google Patents
ホットスタンプ成形体 Download PDFInfo
- Publication number
- WO2019180852A1 WO2019180852A1 PCT/JP2018/011206 JP2018011206W WO2019180852A1 WO 2019180852 A1 WO2019180852 A1 WO 2019180852A1 JP 2018011206 W JP2018011206 W JP 2018011206W WO 2019180852 A1 WO2019180852 A1 WO 2019180852A1
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Classifications
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- C—CHEMISTRY; METALLURGY
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Definitions
- the present invention relates to a hot stamping molded body.
- Structural members used in automobiles and the like are sometimes manufactured by hot stamping (hot pressing) in order to increase both strength and dimensional accuracy.
- hot stamping hot pressing
- the steel sheet is heated to Ac 3 points or more and rapidly cooled while being pressed with a mold. That is, in the manufacturing, pressing and quenching are performed simultaneously. According to the hot stamp, it is possible to produce a molded article with high dimensional accuracy and high strength.
- Patent Documents 1 to 5 propose techniques for suppressing the formation of scale and improving the corrosion resistance by using a plated steel sheet as a hot stamping steel sheet.
- JP 2000-38640 A discloses a steel sheet for hot pressing using Al plating.
- Patent Document 2 discloses a high-strength aluminum-plated steel sheet for automobile members on which an Al plating layer is formed.
- Patent Document 3 discloses a steel sheet for hot pressing in which a Zn plating layer is formed.
- Patent Document 4 discloses a Zn-based plated steel material for hot pressing in which various elements such as Mn are added to the plated layer of the Zn-plated steel sheet.
- Japanese Unexamined Patent Publication No. 2012-112010 discloses a plated steel material using Al—Zn alloy plating.
- JP 2000-38640 A JP 2003-49256 A JP 2003-73774 A JP 2005-113233 A JP 2012-112010 A
- Patent Document 1 scale generation and decarburization during hot stamping are suppressed.
- a hot stamped molded body is mainly composed of Al plating
- the sacrificial corrosion resistance tends to be inferior to a plated steel sheet mainly composed of Zn, and is insufficient from the viewpoint of rust prevention.
- Patent Document 2 relating to a plated steel sheet mainly composed of Al plating has the same problem as described above.
- liquid phase Zn is generated even in an Al—Zn alloy-plated steel sheet to generate LME. Further, in the Al—Zn alloy-plated steel sheet, the plating layer is alloyed, and a large amount of Fe element diffuses from the ground iron in the plating layer, so that red rust may be generated.
- the hot stamping molded body is mainly used as an automobile structural member, spot welding is performed after molding.
- it is effective to set the plating thickness to be thick, but Al and Zn contained in the plating layer react with Cu of the spot electrode and the plating layer is thick.
- the continuous spot spot property of spot welding is significantly lowered. For this reason, it has been difficult to achieve both sufficient corrosion resistance and spot weldability in a hot stamped body of a plated steel sheet.
- the present invention has been made in view of the above problems, and an object thereof is to provide a new and improved molded body having improved fatigue characteristics, corrosion resistance, and spot weldability.
- the present inventors have conducted intensive research on a plated steel sheet having a Zn—Al—Mg based coating layer. As a result, the present inventors obtained the following knowledge.
- FIG. 1 shows a plated steel sheet 10a manufactured under normal conditions.
- the steel material 10a has a plating layer 13a on the surface of the base material 11a. Between the base material 11a and the plating layer 13a, there is a diffusion layer 12a in which Fe of ground iron diffuses into the plating layer.
- FIG. 2 shows a normal hot stamping body 20a.
- the hot stamp molded body 20a has a surface layer portion 2a having a certain thickness on the surface of the base material 1a.
- the surface layer portion 2a has a layered structure including an interface layer 21a and a metal layer 21b in order from the base material 1a, and an oxide layer 4a as the outermost layer.
- the interface layer 21a of the hot stamp formed body 20a is a portion derived from the diffusion layer 12a of the plated steel sheet 10a manufactured under normal conditions.
- the interface layer 21a includes a portion where Fe of the ground iron diffuses into the plating layer 13a during hot stamping.
- the chemical composition of the interface layer 21a differs depending on the chemical composition of the base material 11a and the plating layer 13a.
- the plating layer 13a mainly containing Zn containing Al, Mg, etc. Fe 2 (Al, Zn) 5 , Fe (Al, Zn) 3 Fe -Al phase, such as, further if the plating layer 13a containing a large amount of Si, Fe 3 (Al, Si ), is composed of a Fe-Al-Si phase such as Fe (Al, Si) Layer.
- the oxide layer 4a is an oxide layer mainly composed of Zn.
- the diffusion layer 12a of the plated layer of the plated steel sheet 10a manufactured under normal conditions is thick, it causes various problems during hot stamping. Specifically, Zn in the plating layer 13a is in a liquid phase state when the hot stamp is heated, and is evaporated to decrease the amount of Zn in the metal layer 21b. Moreover, since Zn in the plating layer 13a reacts with the interface layer 21a during hot stamping, the amount of Zn in the metal layer 21b decreases.
- the present inventors have studied the relationship between the plated steel sheet 10a manufactured under normal conditions and the hot stamped molded body 20a, and as a result, determined the thickness of the diffusion layer 12a of the plated steel sheet 10a. The manufacturing conditions for thinning were found.
- the plating bath temperature is set in the range of the melting temperature of plating + 50 ° C. to 100 ° C. in order to form a homogeneous plating layer 13a. This is because, when the temperature of the plating bath approaches the melting temperature, a part of the plating bath is solidified and becomes dross at the time of manufacturing, and the surface cleaning of the plating layer is easily deteriorated.
- the immersion time in the plating bath is usually set to 5 seconds or more.
- the temperature of the steel sheet before entering the plating bath (intrusion plate temperature) is normally maintained at a temperature of the plating bath temperature +0 to ⁇ 15 ° C. The reason is that although it is easy to raise the temperature of the plating bath, it is difficult to lower the temperature of the plating bath, and when the penetration plate temperature is high, it is necessary to cool the plating bath.
- the penetration plate temperature is set to a temperature between the plating bath temperature (° C.) and the plating bath temperature ⁇ 10 (° C.) in all the examples.
- plating bath temperature was about 50 to 100 ° C. of plating temperature
- immersion time was 5 seconds or more
- the intruding plate temperature of the steel plate was plating bath temperature +0 to ⁇ 15 ° C.
- the plated steel sheet 10a is dominant in the plating bath temperature and the immersion time, so that the Fe diffusion to the plating side is easy. Then, the plated steel sheet 10a produced in normal conditions, with reference to FIG.
- the surface layer of the base material (the base steel), Fe 2 (Al, Zn ) 5, Fe (Al, Zn) 3, plating Si
- the diffusion layer 12a made of Fe 3 (Al, Si), Fe (Al, Si), or the like grows thick (1 ⁇ m or more) between the ground iron and the plating layer.
- the present inventors manufactured the plated steel sheet under the conditions of the plating bath temperature different from the normal plating conditions, the immersion time, and the invasion plate temperature of the steel sheet, thereby reducing the thickness of the diffusion layer 12a as compared with the conventional case. I succeeded in making it thinner.
- the first is the temperature and immersion time of the plating bath.
- the diffusion layer 12a such as Fe 2 (Al, Zn) 5 in the plated steel sheet grows to 1 ⁇ m or more, and a thick interface layer is formed on the hot stamped molded body. Formation cannot be avoided.
- the plating bath temperature is lowered as much as possible, specifically, the plating melting temperature +5 to 20 ° C., and the immersion time is limited to 1 to 3 seconds.
- the diffusion layer 12 that grows between the base material (base metal) 11 and the plating layer 13 is a thin layer mainly composed of Fe 2 (Al, Zn) with reference to FIG.
- the plated steel sheet 10 having such a diffusion layer 12 does not grow an interface layer made of Fe 2 (Al, Zn) 5 or the like even if hot stamping is performed thereafter.
- the penetration temperature of the steel sheet into the plating bath was examined.
- the temperature of the plating bath is lowered and the immersion time is shortened, the growth of the diffusion layer 12 such as Fe 2 (Al, Zn) 5 that becomes a thick interface layer in the future can be suppressed.
- the penetration plate temperature is lower than the plating bath temperature, there is a concern that the plating bath is solidified and the cleaning of the plating layer 13 is impaired.
- the penetration temperature was set to the plating bath temperature +5 to 20 ° C.
- Mg combines with Zn in the plating layer 13 to form an MgZn 2 phase 32a. For this reason, molten Zn penetrates during hot stamping, and prevents LME and molten Zn from causing spot weldability deterioration due to cracks inside the steel material. And by making Mg contained in the plating layer 13, it can suppress that Fe of a base material penetrates the diffusion layer 12 which became thin at the time of hot stamping, and is spread
- Mg combines with Zn in the plating layer 13 to form an MgZn 2 phase 32a. For this reason, molten Zn penetrates during hot stamping, and prevents LME and molten Zn from causing spot weldability deterioration due to cracks inside the steel material. And by making Mg contained in the plating layer 13, it can suppress that Fe of a base material penetrates the diffusion layer 12 which became thin at the time of hot stamping, and is spread
- the FeAl 2 phase 32b of the hot stamp molded body is island-shaped. Since this island-shaped FeAl 2 phase 32b is an intermetallic compound having a high melting point, it is considered that it has the effect of improving the continuous spotting property during spot welding and suppressing LME.
- FIG. 3 is a schematic view of a plated steel sheet manufactured under the conditions found by the present inventors as described above.
- FIG. 4 is a schematic view of a hot stamping molded body manufactured by hot stamping a plated steel sheet manufactured under the conditions found by the present inventors as described above.
- the hot stamping molded body 20 manufactured under the conditions found by the present inventors has a thin interface layer 31 and a main layer 32 in a state where the MgZn 2 phase 32a and the island-like FeAl 2 phase 32b are mixed. Is provided. Since the island-shaped FeAl 2 phase 32b is an intermetallic compound having a high melting point, it has the effect of improving the continuous spotting property during spot welding and suppressing LME.
- a hot stamping body comprising a metal layer formed on the surface of the steel base material,
- the metal layer includes, by mass%, Al: 30.0 to 36.0%, a thickness of 100 nm to 5 ⁇ m, an interface layer located at the interface with the steel base material, an MgZn 2 phase, and an island shape FeAl 2 phase is mixed, the thickness is 3 ⁇ m to 40 ⁇ m, and includes a main layer located on the interface layer,
- the average composition of the metal layer is mass%, Al: 20.0-45.0%, Fe: 10.0-45.0%, Mg: 2.0-10.0%, Sb: 0 to 0.5%, Pb: 0 to 0.5%, Cu: 0 to 1.0%, Sn: 0 to 1.0%, Ti: 0 to 1.0%, Ca: 0 to 3.0%, Sr: 0 to 0.5% Cr: 0 to 1.0%, Ni: 0 to 1.0%, Mn: 0 to
- the volume fraction of the FeAl 2 phase is 50.0-80.0%
- the volume fraction of the MgZn 2 phase is 20.0-50.0%.
- the volume fraction of the FeAl 2 phase is 60.0-75.0%, The volume fraction of the MgZn 2 phase is 25.0-45.0%, The hot stamping molded product according to the above (1) or (2).
- FIG. 1 is a schematic view showing a plated steel sheet produced by a normal plating process.
- FIG. 2 is a schematic view showing a hot stamped molded body obtained from a plated steel sheet produced by a normal plating process.
- FIG. 3 is a schematic view showing a plated steel sheet manufactured under the conditions found by the present inventors.
- FIG. 4 is a schematic view showing a hot stamping molded body obtained from a plated steel sheet manufactured under the conditions found by the present inventors.
- FIG. 5 is a reflected electron image of the cross section of the metal layer of the hot stamped article according to one embodiment of the present invention.
- FIG. 6 is a schematic diagram showing the definition of the island-like FeAl 2 phase of the hot stamped article according to one embodiment of the present invention.
- a hot stamp molded body a plated steel sheet for obtaining a hot stamp molded body, and a method for manufacturing the hot stamp molded body according to an embodiment of the present invention will be described.
- “%” about content shall mean “mass%” unless there is particular notice.
- hot stamped molded body 20 includes a steel base material (hereinafter also simply referred to as “base material”) 1 and metal layer 3, and metal layer 3. Is provided with an interface layer 31 and a main layer 32 at the interface with the base material 1, and the main layer 32 is in a state where the MgZn 2 phase 32a and the island-like FeAl 2 phase 32b are mixed. In some cases, the outer surface of the metal layer 3 has an oxide layer 4.
- the chemical composition of the plating layer 13 in particular, the relationship between Zn and Mg components, it is difficult for a layered oxide to be formed in the plating cross section over the entire surface of the plated steel sheet. Therefore, even if the oxide layer 4 is observed, oxides such as Zn, Mg, and Ca components are only partially attached. In addition, the oxide layer 4 may be removed by alkali treatment in a process such as chemical conversion treatment and may not remain on the surface of the final product.
- the base material 1 has the characteristic according to the use of the hot stamping molded object 20 which concerns on this embodiment, there will be no restriction
- steel having the following chemical composition can be used for the base material 1.
- Carbon (C) is an element effective for increasing the strength of the hot stamped molded article, but if the C content is too large, the toughness of the hot stamped molded article is lowered. Therefore, the C content is 0.05% to 0.40%.
- a preferable lower limit of the C content is 0.10%, and a more preferable lower limit of the C content is 0.13%.
- a preferable upper limit of the C content is 0.35%.
- Si 0.5% or less
- Si is an element effective for deoxidizing steel.
- Si in the steel diffuses during heating of the hot stamp to form an oxide on the surface of the steel sheet, resulting in a decrease in the efficiency of the phosphate treatment.
- Si is an element that raises the Ac 3 point of steel. For this reason, excessive inclusion of Si raises the Ac 3 point of the steel sheet and raises the heating temperature of the hot stamp, and thus evaporation of Zn in the plating layer is unavoidable. Therefore, the Si content is 0.5% or less.
- a preferable upper limit value of the Si content is 0.3%, and a more preferable upper limit value of the Si content is 0.2%.
- the preferable lower limit of the Si content varies depending on the required deoxidation level, but is usually 0.05%.
- Mn 0.5% to 2.5%
- Mn Manganese
- a preferable lower limit value of the Mn content is 0.6%, and a more preferable lower limit value of the Mn content is 0.7%.
- the upper limit of preferable Mn content is 2.4%, and the lower limit of more preferable Mn content is 2.3%.
- Phosphorus (P) is an impurity contained in steel. P segregates at the grain boundaries to lower the toughness of the steel and to reduce the delayed fracture resistance. Therefore, the P content is 0.03% or less.
- the P content is preferably as small as possible, and is preferably 0.02% or less. Since excessive reduction of the P content causes an increase in cost, a preferable lower limit is 0.01%.
- S 0.01% or less Sulfur (S) is an impurity contained in steel. S forms sulfides, lowers the toughness of the steel, and lowers the delayed fracture resistance. Therefore, the S content is 0.01% or less.
- the S content is preferably as low as possible, and is preferably 0.005% or less. Since excessive reduction of the S content causes an increase in cost, the preferable lower limit is 0.0001%.
- Al 0.1% or less
- Aluminum (Al) is effective in deoxidizing steel.
- Al is effective in deoxidizing steel.
- excessive inclusion of Al raises the Ac 3 point of the steel sheet and raises the heating temperature of the hot stamp, and thus evaporation of Zn in the plating layer is unavoidable.
- the Al content is 0.1% or less.
- a preferable upper limit value of the Al content is 0.05%, and a more preferable lower limit value of the Al content is 0.01%.
- the Al content is sol. It means the content of Al (acid-soluble Al).
- N 0.01% or less Nitrogen (N) is an impurity inevitably contained in steel. N forms nitrides and lowers the toughness of the steel. When boron (B) is further contained in the steel, N is combined with B to reduce the amount of solute B and lower the hardenability. Therefore, the N content is 0.01% or less.
- the N content is preferably as small as possible, and is preferably 0.005% or less. Since excessive reduction of the N content causes an increase in cost, the preferable lower limit is 0.0001%.
- B 0 to 0.005% Boron (B) increases the hardenability of the steel and increases the strength of the steel sheet after hot stamping, so it may be contained in the base material. However, the effect is saturated even if it contains B excessively. Therefore, the B content is 0 to 0.005%. A preferable lower limit of the B content is 0.0001%.
- Titanium (Ti) can combine with nitrogen (N) to form a nitride, and suppress the decrease in hardenability due to BN formation. Ti can also reduce the austenite grain size during heating of the hot stamp and enhance the toughness of the steel sheet due to the pinning effect. Therefore, Ti may be contained in the base material. However, even if Ti is excessively contained, the above effect is saturated, and when Ti nitride is excessively precipitated, the toughness of the steel is lowered. Therefore, the Ti content is 0 to 0.1%. A preferable lower limit of the Ti content is 0.01%.
- Chromium 0 to 0.5% Chromium (Cr) is effective in enhancing the hardenability of the steel and increasing the strength of the hot stamped product, and therefore may be contained in the base material. However, if the Cr content is excessive and a large amount of Cr carbide that is difficult to dissolve during heating of the hot stamp is formed, the austenitization of the steel is difficult to proceed, and conversely the hardenability is lowered. Therefore, the Cr content is 0 to 0.5%. Moreover, the lower limit of the preferable Cr content is 0.1%.
- Mo 0 to 0.5% Molybdenum (Mo) may be included in the base material because it enhances the hardenability of the steel. However, even if Mo is excessively contained, the above effect is saturated. Therefore, the Mo content is 0 to 0.5%. Moreover, the lower limit of preferable Mo content is 0.05%.
- Niobium (Nb) is an element that forms carbides, refines the crystal grains at the time of hot stamping, and increases the toughness of the steel. Therefore, niobium (Nb) may be contained in the base material. However, when Nb is contained excessively, the above effect is saturated and the hardenability is further lowered. Therefore, the Nb content is 0 to 0.1%. The lower limit of the preferable Nb content is 0.02%.
- Nickel (Ni) may be contained in the base material because it can suppress embrittlement caused by molten Zn during heating of the hot stamp. However, the above effect is saturated even if Ni is contained excessively. Therefore, the Ni content is 0 to 1.0%. A preferable lower limit of the Ni content is 0.1%.
- the balance of the chemical composition of the base material constituting the hot stamping molded body according to the present embodiment is Fe and impurities.
- an impurity is a component that can be contained in ore or scrap as a raw material or a component that can be mixed due to a manufacturing environment or the like when industrially manufacturing steel materials. It is a component that is allowed as long as the effect is not hindered.
- the interface layer 31 is a layer in which the Al component in the plating layer is diffused into the base material (base metal) by heating of the hot stamp and is combined with Fe. It is composed of an Al-based intermetallic compound (hereinafter also simply referred to as “Fe—Al”).
- Fe—Al is an intermetallic compound with a fixed atomic ratio.
- the elemental composition ratio (% by mass) of Fe—Al is Al: about 33% and Fe: about 67%.
- TEM Transmission Electron Microscope
- an Al 3 Fe phase having a high Al concentration is formed on the extreme surface layer of the interface layer 31 as a fine precipitate that does not form a layer, and an Fe 3 Al phase or the like is formed in the vicinity of the base material.
- the Al content of the interface layer is set in the range of 30.0 to 36.0%.
- the Fe-Al-based intermetallic compound may contain a small amount of Zn, Mn, Ni, or the like as a solid solution in Fe-Al, depending on the base metal of the plated steel sheet and the chemical composition of the plating layer. Therefore, it can be said that the Fe—Al-based intermetallic compound includes Al: 30.0 to 36.0%, and the balance is substantially Fe.
- substantially means that the content of other components (for example, Zn, Mn, Si, and Ni) of less than 3% is allowed.
- the interface layer becomes a barrier coating of the base material and has a certain corrosion resistance. Therefore, the interfacial layer prevents elution of the base iron during under-coating corrosion, and flow red rust generated from cut flaws in corrosion tests, etc. (specifically, red rust that forms streaks from cut flaws) ) Can be suppressed.
- the thickness of the interface layer is set to 100 nm or more. However, if the interface layer is too thick, red rust formed from Fe—Al itself flows and becomes red rust, so the thickness of the interface layer is set to 5 ⁇ m or less. Therefore, the thickness of the interface layer is 100 nm or more and 5 ⁇ m or less.
- the lower limit of the thickness of the interface layer is preferably 500 nm and the upper limit is preferably 2 ⁇ m in order to confirm a clear rust inhibitory effect. The upper limit is more preferably 1 ⁇ m.
- main layer 32 is a layer in which MgZn 2 phase 32 a and island-like FeAl 2 phase 32 b are mixed.
- the main layer 32 has an effect of suppressing scale generation at the time of hot stamping, and bears the corrosion resistance of the hot stamping molded body 20.
- the corrosion resistance of the hot stamped molded product 20 is that the main layer 32 is sacrificed to prevent red rust from being generated by the sacrificial corrosion protection, and the main layer 32 is in close contact with the upper layer coating film (not shown). It is exhibited by the action that ensures the property and does not extend the rust range.
- the state where the MgZn 2 phase 32a and the island-like FeAl 2 phase 32b coexist means that the island-like FeAl 2 phase 32b is dispersed (spotted) throughout the main layer 32.
- a specific state of the island-like FeAl 2 phase 32b is shown in FIG.
- the island FeAl 2-phase 32b, in addition to those present in a island FeAl 2 phase 32b alone, also includes a plurality of islands FeAl 2 phase 32b adjacent are aggregated.
- the FeAl 2 phase 32b of the present invention is characterized by an island shape.
- the projected length of the FeAl 2 phase 32b on the interface between the metal layer 3 and the base material 1 is 2d (see 2d 1 , 2d 2 , 2d 3 , 2d 4 in FIG. 6), and the perimeter of the FeAl 2 phase 32b And L was calculated from the measured 2d and L using the following formula, and an FeAl 2 phase having R of 2 or more was assumed to be island-shaped.
- R L / 2d ⁇ 2
- the island-like FeAl 2 phase 32b does not grow in the form of a layer from the ground iron side into the plating layer at the interface between the plating layer and the ground iron, but grows by spherical nucleation in the plating layer. When the actual cross-sectional structure is observed, the spherical phases are in contact and fixed. Since the island-like FeAl 2 phase 32b grows spherically three-dimensionally, compared to the layered FeAl 2 phase at the plating layer / ground iron interface formed by a normal manufacturing method, MgZn 2 in the main layer is formed. Large contact area with phase.
- the diffusion layer 12 (Fe 2 (Al, Zn) 5 etc.) of the plated steel sheet 10 before hot stamping of the present invention has a thin thickness of less than 1 ⁇ m and a small amount of Si solid solution in the diffusion layer 12. Therefore, the chemical bond is not so strong. Therefore, a trace amount of Fe is dispersed in the plating layer 13 through the diffusion layer 12 when the plated steel sheet 10 is manufactured. Further, even during the heating of the hot stamp, Fe in the base material diffuses through the diffusion layer 12 and into the plating layer 13 in a molten state. It is inferred that the microdispersed Fe in the plating layer is bonded to Al atoms and Zn atoms as nucleation sites during hot stamping and grows in an island shape.
- the island-like FeAl 2 phase When the island-like FeAl 2 phase is formed, 0.05 to 0.5% Fe is detected by analyzing a solution dissolved with fuming nitric acid with respect to the plating layer 13 before heating.
- the interface layer 21a such as Fe 2 (Al, Zn) 5 or the like. It is considered that the hot stamping molded product 20a obtained by growing the layer has a layered structure.
- the component concentration is almost constant from the atomic ratio, the Mg concentration is about 16.0%, and the Zn concentration is about 84.0%.
- Al may be dissolved in the range of 0 to 8.0% and Fe may be dissolved in the range of 0 to 5.0%, so the Mg concentration is 13.0 to
- the Zn concentration is defined in the range of 20.0%, and the Zn concentration is defined in the range of 70.0-87.0%.
- the balance other than these components is impurities. Examples of the impurities include 0 to 0.01% Ni, 0 to 0.01% Si, and the like.
- the component concentration is almost constant from the atomic ratio, and both the Al concentration and the Fe concentration are about 50.0%.
- Zn may be dissolved in the range of 0 to 15.0%, so the Al concentration is defined in the range of 40.0 to 55.0%, and the Fe concentration is It is defined in the range of 40.0 to 55.0%.
- the balance other than these components is impurities. Examples of the impurities include 0 to 0.01% Ni, 0 to 0.01% Si, and the like.
- the FeAl 2 phase 32b Since the FeAl 2 phase 32b is changed from a layered state to an island shape, the Al component in the MgZn 2 phase 32a in the metal layer is reduced, so that the continuous spotting property at the time of spot welding is improved. This is because the Al component present in the MgZn 2 phase 32a reacts with the spot-welded Cu electrode to significantly reduce the continuous spotting property.
- the FeAl 2 phase since the FeAl 2 phase is not in a layer form but in an island form, penetration of molten Zn generated during hot stamping into the base material is suppressed, and LME is suppressed. However, simply increasing the amount of the FeAl 2 phase 32b may deteriorate the corrosion resistance, so the balance between the amount and form of the FeAl 2 phase is important.
- the size of the island-shaped FeAl 2 phase 32b is not particularly limited, but if it is too large, it may be unevenly distributed in the main layer 32. If the island-like FeAl 2 phase 32b is unevenly distributed, the corrosion resistance and chipping resistance may be adversely affected. For this reason, the size of the island-like FeAl 2 phase 32b is preferably as small as possible and preferably not unevenly distributed.
- the corrosion resistance improves as the amount of MgZn 2 phase increases.
- the MgZn 2 phase 32a prevents solid solution of Zn in the main phase layer, and suppresses generation of liquid phase Zn during heating of the hot stamp. Liquid phase Zn is also generated at the time of spot welding and reacts with the Cu electrode to lower the continuous spot property.
- the MgZn 2 phase 32a By causing the MgZn 2 phase 32a to be present in the main layer 32, the generation of the liquid phase Zn can be suppressed, and the decrease in continuous spotting property can also be suppressed.
- the amount of MgZn 2 phase is too large, at the time of hot stamping, or plating layer is deposited on the mold, possibly LME by region Zn concentration is high in MgZn 2 Aiuchi is generated or generated is there.
- the volume fraction of the FeAl 2 phase 32b is preferably 50.0 to 80.0%, and the volume fraction of the MgZn 2 phase 32a is preferably 20.0 to 50.0%. Within this range, excellent corrosion resistance, spot weldability, LME property, and mold weldability are easily obtained.
- the volume fraction of the FeAl 2 phase 32b is preferably 60.0-75.0%, and the volume fraction of the MgZn 2 phase 32a is preferably 25.0-40.0%.
- the thickness of the main layer 32 is set to 3 ⁇ m or more.
- the thickness of the main layer 32 is set to 40 ⁇ m or less.
- the lower limit of the thickness of the main layer 32 is preferably 6 ⁇ m, and more preferably 10 ⁇ m.
- the upper limit of the thickness of the main layer 32 is preferably 30 ⁇ m, and more preferably 25 ⁇ m.
- Metal layer 3 has the following average composition.
- Al 20.0-45.0%
- Al forms an interface layer 31 in the vicinity of the interface between the base material 1 and the metal layer 3 by heating at the time of hot stamping, and generates FeAl 2 phase 32b in the main layer 32. It is an essential element for suppressing excessive diffusion in the layer 32. If the Al content in the metal layer 3 is too small, the thickness of the interface layer 31 is reduced, Fe is likely to diffuse from the base material 1 to the main layer 32, and the Fe content that dissolves in the MgZn 2 phase 32a is reduced. Get higher. Further, the FeAl 2 phase 32b in the main layer 32 is reduced. As a result, it leads to a decrease in spot weldability, the occurrence of LME, and the occurrence of welding during hot stamping. Therefore, the lower limit of the Al content in the metal layer 3 is 20.0%.
- the upper limit of the Al content in the metal layer 3 is 45.0%.
- the preferable lower limit of the Al content is 25.0%, and the more preferable lower limit is 29.0%.
- the upper limit with preferable Al content is 44.0%, and a more preferable upper limit is 38.0%.
- Fe 10.0-45.0%
- Fe diffuses from the base material 1 to the metal layer 3, so that the metal layer 3 of the hot stamp formed body 20 always contains Fe.
- Fe combines with Al in the metal layer 3 to form the FeAl 2 phase 32 b in the interface layer 31 and the main layer 32.
- the Fe concentration in the metal layer 3 increases as the thickness of the interface layer 31 increases and the amount of the FeAl 2 phase 32b in the main layer 32 increases.
- the Fe concentration is low, the amount of the FeAl 2 phase 32b is also reduced, so that the structure of the main layer 32 is easily broken.
- the upper limit of the Fe content of the metal layer 3 is 45.0%.
- the lower limit of the Fe content of the metal layer 3 is preferably 20.0%, more preferably 27.0%, and even more preferably 32.5%.
- the upper limit of the Fe content of the metal layer 3 is preferably 42.0%, and more preferably 36.5%.
- Mg 2.0-10.0%
- Mg is an element effective for improving the corrosion resistance of the metal layer 3 and improving the swollen width under the coating film in the corrosion test.
- Mg combines with the Zn component in the metal layer 3 to prevent the generation of liquid phase Zn during heating of the hot stamp, and thus has an effect of suppressing LME cracking.
- the Mg content is set to 2.0% or more.
- the upper limit of the Mg content is 10.0%.
- the Mg content is preferably 3.0% or more, and more preferably 3.5% or more.
- Sb 0 to 0.5%
- Pb 0 to 0.5%
- Cu 0 to 1.0%
- Sn 0 to 1.0%
- Ti 0 to 1.0%
- Sb, Pb, Cu, Sn, and Ti are substituted with Zn in the metal layer 3 to form a solid solution in the MgZn 2 phase, but if it is within a predetermined content range, the hot stamped molded body 20 is adversely affected. Does not affect. Therefore, these elements may be included in the metal layer 3. However, if the content of each element is excessive, oxides of these elements are precipitated during heating of the hot stamp, and the surface properties of the hot stamp molded body 20 are deteriorated, resulting in poor phosphorylation treatment. Corrosion resistance after painting tends to deteriorate.
- the Sb and Pb contents are 0.5% or less, and the Cu, Sn and Ti contents are 1.0% or less.
- the content of Sb and Pb is preferably 0.2% or less, and the content of Cu, Sn and Ti is preferably 0.8% or less, and more preferably 0.5% or less.
- Ca and Sr can suppress the formation of top dross formed on the plating bath during production. Moreover, since Ca and Sr tend to suppress atmospheric oxidation during the heat treatment of the hot stamp, the color change of the plated steel sheet after the heat treatment can be suppressed. Since these effects are stronger in Sr than Ca, Sr is more effective in a small amount. Moreover, when content of these elements is excessive, it has a bad influence on a coating film swelling width and flow rust in a corrosion test. Therefore, one or more selected from Ca and Sr may be contained in the metal layer 3 in a range where the Ca content is 3.0% or less and the Sr content is 0.5% or less.
- the Ca content is preferably 2.0% or less, and more preferably 1.5% or less.
- the Sr content is preferably 0.3% or less, and more preferably 0.1% or less.
- the Ca content is preferably 0.1% or more, and the Sr content is preferably 0.05% or more.
- Mn: 0 to 1.0% Cr, Ni, and Mn are concentrated in the vicinity of the interface between the plating layer and the base material in the plated steel sheet and have the effect of eliminating spangles on the surface of the plating layer.
- These elements are substituted with Fe in the metal layer 3 of the hot stamping molded body 20 and are contained in the interface layer 31 or form a solid solution in the FeAl 2 phase 32 b in the main layer 32. Therefore, one or more selected from Cr, Ni and Mn may be included in the metal layer 3.
- the contents of Cr, Ni and Mn are each set to 1.0% or less.
- the content of Cr, Ni and Mn is preferably 0.5%, more preferably 0.1% or less.
- the lower limit for the content of Cr, Ni and Mn is preferably 0.01%.
- Si 0 to 1.0% Si is an element that greatly reduces the activity of Zn and Al in the molten state and greatly affects the diffusion of Fe and the elements constituting the metal layer 3 during hot stamping. Therefore, since Si may greatly collapse the dispersion structure of the FeAl 2 phase 32b, it is necessary to limit the content to an appropriate content.
- the Si content in the metal layer 3 is excessive, the MgZn 2 phase 32a in the metal layer 3 decreases, and an Mg 2 Si phase is formed starting from the interface between the base material and the metal layer, resulting in a significant deterioration in corrosion resistance. To do. Further, due to the decrease in the MgZn 2 phase, the free Zn forms the Zn phase, and thus LME may be generated.
- Si suppresses the diffusion of Fe into the metal layer 3 and inhibits the growth of the interface layer 31 and the growth of the FeAl 2 phase 32b. For this reason, it is preferable to reduce Si content as much as possible, and set it as 1.0% or less.
- the Si content is preferably 0.2% or less, and more preferably 0%.
- Remainder 12.0 to 45.0% of Zn and impurities
- Zn and impurities In the metal layer 3, it is essential to contain Zn from the viewpoint of rust prevention. Most of the Zn component contained in the metal layer 3 exists as the MgZn 2 phase 32a. On the other hand, since Zn atoms can be substituted with Al atoms, Zn can be dissolved in the FeAl 2 phase 32b even though the amount is small. Therefore, when the amount of the MgZn 2 phase 32a contained in the metal layer increases, the Zn concentration in the metal layer 3 also increases.
- the hot stamped molded body 20 when the hot stamped molded body 20 is subjected to a corrosion test, the MgZn 2 phase 32a is eluted and white rust is generated. appear.
- the Zn content in the metal layer 3 is low and there is almost no intermetallic compound containing no Fe such as MgZn 2 phase, the hot stamped molded product contains Fe in the metal layer when subjected to a corrosion test. Intermetallic compounds corrode and red rust is generated. That is, whether white rust or red rust is generated during corrosion is closely related to the Zn content in the metal layer 3 and the presence of the MgZn 2 phase 32a in the main layer 32.
- the Zn content in the metal layer 3 is 12.0% or more, white rust is generated in the corrosion test from the coating cross-cut flaw, but the Zn content in the metal layer 3 is 12 If it is less than 0%, red rust is generated immediately. For this reason, Zn content in the metal layer 3 shall be 12.0% or more.
- the Zn phase which does not react with Mg in the metal layer 3 will precipitate. The precipitation of the Zn phase may generate LME, and as a result, may deteriorate the fatigue strength of the hot stamped article. Therefore, the Zn content is 45.0% or less.
- the minimum with preferable Zn content is 16.5%, and a more preferable minimum is 18.5%.
- the upper limit with preferable Zn content is 40.0%, and a more preferable upper limit is 32.0%.
- the remainder of the metal layer 3 is 12.0 to 45.0% Zn and impurities.
- Arbitrary elements other than those described above may be included as impurities in a range that does not interfere with the effects of the present invention.
- the oxide layer 4 may be formed in the outermost layer of the hot stamp molded body 20 according to the present embodiment by oxidation of a plating component. Since the oxide layer 4 may deteriorate the phosphorylation property and electrodeposition coating property provided after hot stamping, the oxide layer 4 is preferably thin. When the thickness is 1.0 ⁇ m or less, the main performance of the metal layer 3 is not affected.
- the plated steel sheet 10 used for obtaining the hot stamping molded body 20 according to the present embodiment includes a diffusion layer 12 between a base material (base metal) 11 and a plating layer 13. Since the chemical composition of the base material 11 is the same as the chemical composition of the base material 1 of the hot stamp molded body 20 according to the present embodiment, the description thereof is omitted.
- the diffusion layer 12 is a thin layer mainly composed of Fe 2 (Al, Zn).
- the plating layer 13 is a Zn—Al—Mg-based plating layer, and is not particularly limited as long as it forms the metal layer 3 having the above-described chemical composition after hot stamping.
- a layer having the following chemical composition can be used as the plating layer 13, for example.
- Zn 17.0% or more Zn is an essential element for forming the MgZn 2 phase 32a in the main layer 32 of the hot stamping body 20 according to the present embodiment, and its content is 17.0% or more. It is recommended that
- Al 10.0-70.0%
- Al is an essential element for forming the island-shaped FeAl 2 phase 32b in the main layer 32 of the hot stamping body 20 according to the present embodiment, and its content is 10.0 to 70.0%. It is recommended to do.
- Mg 7.0-20.0%
- Mg is an essential element for forming the MgZn 2 phase 32a in the main layer 32 of the hot stamping molded body 20 according to the present embodiment, and its content should be 7.0 to 20.0%.
- Recommended. Mg in this range suppresses excessive reaction between Zn, Al in a molten state, or a mixture of Zn and Al and the ground iron.
- Fe 0.05 to 2.0% Fe is recommended to have a content of 0.05% or more in order to precipitate an island-like FeAl 2 phase during hot stamping heating. On the other hand, in order to suppress an excessive alloying reaction during hot stamping, the Fe content is preferably 2.0% or less.
- Fe in the plating layer includes not only those contained in the plating bath but also those derived from the base material.
- Si 0 to 1.0% If the content of Si is too large, it reacts with Mg during hot stamping to form a Mg 2 Si phase, and the corrosion resistance is greatly deteriorated. Therefore, the content is preferably 1.0% or less.
- the plating layer 13 may further contain the following elements.
- the content of these elements hardly changes before and after hot stamping. Further, the range of the content of each element is the same as the description in the metal layer 3, and therefore will be omitted.
- Mn 0 to 1.0%
- the plating layer 13 may contain any element other than the above as an impurity as long as the effect of the present invention is not hindered.
- the thickness of the plating layer 13 may be 3 to 50 ⁇ m, for example. Moreover, the plating layer 13 may be provided on both surfaces of the steel plate, or may be provided only on one surface of the steel plate.
- the method for manufacturing a hot stamped article according to the present embodiment includes a step of preparing a base material (base material preparation step) and a step of forming a Zn—Al—Mg plating layer on the base material to prepare a plated steel sheet (plating) Processing step) and a step of performing hot stamping on the plated steel sheet (hot pressing step), and if necessary, a rust preventive oil film forming step and a blanking step.
- base material preparation step base material preparation step
- a step of forming a Zn—Al—Mg plating layer on the base material to prepare a plated steel sheet (plating) Processing step
- a step of performing hot stamping on the plated steel sheet hot pressing step
- This step is a step of preparing a base material.
- molten steel having the above-described chemical composition is manufactured, and a slab is manufactured by a casting method using the manufactured molten steel. Or you may manufacture an ingot by the ingot-making method using the manufactured molten steel.
- a base material is manufactured by hot rolling the manufactured slab or ingot.
- This step is a step of forming a Zn—Al—Mg plating layer on the base material.
- the Zn—Al—Mg plating layer having the above-described composition is formed on both surfaces of the base material.
- the adhesion amount of the plating layer is preferably 170.0 g / m 2 or less per side.
- various types of pre-plating such as Ni pre-plating and Sn pre-plating can be applied as an auxiliary to plating adhesion. However, since various types of pre-plating change the alloying reaction,
- the adhesion amount is preferably 2.0 g / m 2 or less per side.
- the diffusion layer 12a such as Fe 2 (Al, Zn) 5 in the plated steel sheet grows to 1 ⁇ m or more, and a thick interface layer is formed on the hot stamped molded body. Formation cannot be avoided. Moreover, even if the temperature of the plating bath is reduced, the same problem occurs when the immersion time is too long. For this reason, it is preferable to reduce the plating bath temperature as much as possible, specifically, to limit the melting temperature of the plating +5 to 20 ° C., and to limit the immersion time to 1 to 3 seconds.
- the diffusion layer 12 that grows between the base material (base metal) 11 and the plating layer 13 is a thin layer mainly composed of Fe 2 (Al, Zn) with reference to FIG.
- the plated steel sheet 10 having such a diffusion layer 12 does not grow an interface layer made of Fe 2 (Al, Zn) 5 or the like even if hot stamping is performed thereafter.
- the penetration plate temperature is preferably set to the plating bath temperature +5 to + 20 ° C.
- This step is a step of performing hot stamping on the above-described plated steel sheet after mild heating.
- the plated steel sheet is heated mainly using energization heating (Joule heat) or radiant heat.
- the plated steel sheet is inserted into a heating furnace, and the plated steel sheet is soaked at 900 ° C., which is a temperature of three or more points of the steel sheet. It is cooled at the same time as pressing by sandwiching it with a flat plate mold. In addition, it takes about 5 seconds to take out the heated plated steel sheet from the furnace and start cooling, and the cooling is started when the temperature of the plated steel sheet is about 800 ° C. In addition, cooling is performed so that the cooling rate to the martensitic transformation start point (410 ° C.) is 50 ° C./second or more even in a portion where the cooling rate of the plated steel sheet is low.
- 900 ° C. is a temperature of three or more points of the steel sheet. It is cooled at the same time as pressing by sandwiching it with a flat plate mold. In addition, it takes about 5 seconds to take out the heated plated steel sheet from the furnace and start cooling, and the cooling is started when the temperature of the plated steel sheet is about 800 °
- the heating rate in the heating process is preferably 10 ° C./second or more, more preferably 30 ° C./second or more.
- the holding time for soaking is preferably 900 ° C. for 60 seconds or shorter, and more preferably 30 seconds or shorter.
- the hot stamping body can be obtained from the plated steel sheet by the above hot stamping process.
- the plated steel sheet is exposed to a high temperature, but since the plating layer suppresses oxidation of the base iron, scale formation can be suppressed.
- the manufacturing method of the hot stamping body which concerns on this embodiment from the preparation of the base material of a plated steel plate was demonstrated, it is not limited to the said description.
- the hot stamping molded body according to the present embodiment can be manufactured by hot stamping a plated steel sheet having a desired plating layer purchased from the market.
- the process which can be selected arbitrarily in the said manufacturing method is written together.
- This step is a step of forming a rust-preventing oil film by applying a rust-preventing oil to the surface of the hot stamped plated steel sheet after the plating treatment step and before the hot stamping step. If a long period of time has elapsed from the production of a hot stamped plated steel plate to the hot stamping, the surface of the plated steel plate may be oxidized. However, the surface of the plated steel sheet on which the rust-preventing oil film is formed by this step is not easily oxidized, thereby suppressing the formation of scale. In addition, a well-known technique can be used suitably for the formation method of a rust prevention oil film.
- the plated steel plate is processed into a specific shape by performing at least one of shearing or punching on the hot stamped plated steel plate. It is a process.
- the sheared surface of the plated steel sheet after blanking is easy to oxidize.
- the sheared surface of the plated steel sheet is also rust-prevented. By spreading the oil to some extent, oxidation of the plated steel sheet after blanking can be suppressed.
- the thickness of each of the metal layer 3, the interface layer 31, and the main layer 32 of the hot stamp molded body 20 according to the present embodiment is cut out from the hot stamp molded body 20, embedded in a resin, etc., and then cross-section polished. This can be determined by measuring the SEM observation image. Further, when observation is performed with a reflected electron image in the SEM, the contrast at the time of observation differs depending on the metal component, so that each layer can be identified and the thickness of each layer can be confirmed.
- line analysis is performed, and the position where the Al concentration is 30.0 to 36.0% is determined. What is necessary is just to specify the interface of the layer 31 and the main layer 32. In three or more different visual fields, the same tissue structure is observed, and the average thickness in each visual field is calculated, and this is set as the thickness of each of the metal layer 3, the interface layer 31, and the main layer 32.
- the thickness of each layer can be accurately grasped by using a mapping image or the like by EPMA (Electron Probe MicroAnalyzer).
- EPMA Electro Probe MicroAnalyzer
- using a pre-determined alloy create a calibration curve for quantitative analysis using a high-frequency glow discharge emission spectrometer (GDS) to understand the element strength distribution in the depth direction of the target layer.
- GDS glow discharge emission spectrometer
- the thickness of each layer can also be determined. For example, in the GDS analysis of ⁇ 5 mm, the component of the place where the component strength in the depth direction becomes almost flat may be grasped, and the average value may be adopted from the measurement results of five or more locations to determine the thickness of each layer. .
- the chemical composition of the entire metal layer 3 is such that the metal layer 3 is dissolved in an acid solution to which an inhibitor that suppresses corrosion of the ground iron is added, and the peeling solution of the metal layer 3 is obtained by ICP (high frequency inductively coupled plasma) emission spectroscopy. It can be confirmed by measuring. In this case, what is measured is the total average component value of the interface layer 31 and the main layer 32.
- the average composition of the plating layer before heating can be confirmed by dissolving the plating layer using fuming nitric acid and measuring the stripping solution by ICP emission spectroscopy.
- fuming nitric acid is used, and if fuming nitric acid is used, the influence of the Fe-Al intermetallic compound can be left without being dissolved, and the concentration of Fe contained only in the plating layer can be measured. Because.
- the component values of the MgZn 2 phase 32a and the FeAl 2 phase 32b in the main layer 32 are preferably subjected to quantitative analysis by SEM-EDX, EPMA observation or the like. In this case, it is preferable that quantitative analysis is performed at a plurality of locations having the same tissue structure, and an average value of these is adopted as a component value. In determining the components of each phase, it is preferable to employ an average value of at least 10 locations.
- the volume fraction of the MgZn 2 phase 32a and the FeAl 2 phase 32b in the main layer 32 can be calculated by performing computer image processing from the SEM reflected electron image of the main layer 32 in an arbitrary cross section.
- the area ratio of each phase may be simply measured by binarization.
- the volume fraction of the MgZn 2 phase 32a and FeAl 2 phases 32b measures at least 5 cross-section (5 fields) more than the area ratio of MgZn 2 phase 32a and FeAl 2 phases 32b from the reflected electron image of SEM
- the average of the measured area ratio is defined as the volume fraction of each phase in the main layer 32 as it is.
- the corrosion resistance of the metal layer 3 is most preferably evaluated by using an exposure test that can provide data that matches the actual environment.
- the corrosion resistance test is performed in a corrosion acceleration test. May be.
- the corrosion resistance can be evaluated by performing a salt spray test or a combined cycle corrosion test and judging the occurrence of white rust or red rust.
- Hot stamped moldings are often used after being painted, so the hot stamped moldings may be pre-painted for automobiles, and if necessary, the surface of the hot stamped moldings may be cut. Also good.
- Spot weldability is evaluated by using a spot welder, performing a weld lobe test on a plated steel sheet that has been heat-treated equivalent to a hot stamp, measuring the appropriate current value, and then performing a continuous spot test.
- spot weldability can be evaluated by setting the nugget diameter at the start to 6 mm and measuring the number of hit points until the nugget diameter falls below 4 ⁇ t (t is the thickness of the steel sheet).
- the occurrence of LME can be confirmed by observing a cracked portion from the metal layer 3 with a test piece subjected to a bending test after hot stamping. Specifically, the hot stamped molded body is immediately subjected to a V-bending test or the like, and a test piece subjected to the V-bending test is embedded in a resin or the like, surface-polished, and confirmed by observing a cracked portion from the metal layer 3. I can. At the same time, it is possible to determine whether or not the plating layer is welded during hot stamping by observing the mold used for the bending test.
- the FeAl 2 phase 32b when the FeAl 2 phase 32b is less than 2.0, the FeAl 2 phase 32b is assumed to be layered.
- the FeAl 2 phase 32b was less than 2.0, the FeAl 2 phase 32b was almost in the same state as a conventional hot stamped product, and there were very few FeAl 2 phases 32b that could be used for measuring the R value.
- a base material constituting a hot stamping molded body was prepared. That is, a slab was manufactured by a continuous casting method using molten steel containing the chemical composition shown in Table 1 and the balance being Fe and impurities. Subsequently, the slab was hot-rolled to produce a hot-rolled steel sheet, and the hot-rolled steel sheet was further pickled, and then cold-rolled to produce a cold-rolled steel sheet. The manufactured cold-rolled steel sheet was used as a base material (plate thickness was 1.4 mm or 0.8 mm) for a plated steel sheet used for hot stamping.
- the comparative examples 45 and 46 are respectively an Al alloy-plated steel sheet and an galvannealed steel sheet that have been conventionally used as plated steel sheets for hot stamping. Specifically, no.
- the comparative example No. 45 is an Al-10% Si alloy plated steel sheet.
- a comparative example of 46 is a Zn-11% Fe alloyed galvanized steel sheet.
- Hot stamping is a mold equipped with a water-cooled jacket after setting the furnace temperature of the heating furnace to 900 ° C, which is the temperature of Ac 3 points or more of the steel sheet, charging the plated steel sheet into the heating furnace and heating it at 900 ° C. It was carried out by pressing with. Two types of hot stamping were performed by changing the heat treatment conditions.
- the heating method of the hot stamp is energization heating, the both ends of the steel plate are sandwiched between electrodes, the temperature is raised from room temperature to 900 ° C. at 50 ° C./second, and held for 30 seconds.
- the hot stamping body was manufactured by taking out and immediately hot-stamping by inserting a steel plate into a flat plate mold equipped with a water-cooling jacket. At this time, in the heating furnace, the oxygen concentration in the furnace was controlled to be less than 18% by performing a nitrogen flow.
- the heating method of the hot stamp is radiant heat heating in an open air furnace, the temperature is raised from room temperature to 900 ° C. at 120 ° C. at 5 to 10 ° C./s for 120 seconds, and then held for 60 seconds.
- the steel sheet was taken out and immediately subjected to hot stamping by inserting the steel sheet into a flat plate mold equipped with a water cooling jacket to produce a hot stamping body.
- the cooling conditions are the same for both heat treatments A and B, and quenching is controlled so that the cooling rate is 50 ° C./second or higher up to the martensite transformation start point (410 ° C.) even at a low cooling rate. did. Moreover, the sample was cut out from the hot stamping molded object as needed.
- a cut plate sample was cut out from the manufactured hot stamping molded body, plated and peeled off, and the chemical composition of the metal layer of the hot stamping molded body was measured. Also, the thickness of the interface layer and main layer is measured by embedding the cut plate with resin and quantitative analysis is performed by SEM-EDX or EPMA analysis, and the components of Al 2 Fe phase and MgZn 2 phase are quantitatively determined. analyzed. The results are shown in Tables 6-9.
- Table 10 and Table 11 show the performance of the hot stamping compacts.
- the test method of each performance is as follows.
- the steel plate was taken out from the heating furnace and immediately subjected to hot V bending using a large press.
- the time from the start of taking out the steel plate from the heating furnace to the start of the processing of the steel plate was set to 5 seconds.
- the steel was quenched to a martensite transformation start point (410 ° C.) at a cooling rate of 50 ° C./second or more.
- the shape of the mold was such that the outer part of the bending radius by the V bending process was extended by about 15% at the end of the bending process.
- the cross section in the thickness direction of the steel sheet at the V-bending site was observed using an SEM and a backscattered electron detector, and the presence or absence of liquid metal embrittlement cracking (LME) was confirmed by confirming the backscattered electron image.
- LME liquid metal embrittlement cracking
- a cationic electrodeposition paint manufactured by Nippon Paint Co., Ltd. was applied by electrodeposition with a slope of 160 V on the plate-shaped hot stamped molded body of each test number, Furthermore, baking painting was performed at a baking temperature of 170 ° C. for 20 minutes. The average film thickness of the paint after electrodeposition coating was 15 ⁇ m for all samples.
- red rust resistance was evaluated by putting a cross-cut into the hot stamped molded body after the coating until reaching the steel material and conducting a combined cycle corrosion test (JASO M609-91). As a specific evaluation method, the time until red rust occurred was evaluated. Those with red rust occurring at 30 cycles of the above combined cycle corrosion test are evaluated as “B” (bad), those with red rust occurring at 60 cycles are evaluated as “A” (slightly good), and 90 cycles Those in which red rust occurred at the time were evaluated as “AA” (good), and those in which red rust did not occur even after 150 cycles or more were evaluated as “AAA” (best). And evaluation "A” or more was made into the pass. The results are also shown in Table 10 and Table 11.
- the maximum swollen width of the coating film from the cut flaw was calculated as an average of 8 points around the cross cut, and the coating film swelling property was evaluated. Films with a swollen width of 3 mm or more at 120 cycles are evaluated as “B” (defect), and those with a swollen film width of 2 to 3 mm are evaluated as “A” (good). Of less than 2 mm was evaluated as “AAA” (best). And evaluation "A” or more was made into the pass. The results are also shown in Table 10 and Table 11.
- the flow rust (rust sagging width) from the tip of the swelled portion of the coating to the tip of the rust-attached portion is calculated as an average of 8 points around the crosscut, and the flow rust width is measured did.
- the flow rust width at 120 cycles is 5 mm or more, it is evaluated as “B” (defect), and when the flow rust width is 3 mm to 5 mm, it is evaluated as “A” (good), and the flow rust width is less than 3 mm.
- the welding conditions were a pressure of 1860 N, a squeeze time of 30 cycles, an upslope of 3 cycles, an energization time of 7 cycles, a hold time of 25 cycles, an electrode used: Obara DHOM type, and 20 points of preliminary hits.
- the nugget diameter was measured by peel peeling, and the button diameter was evaluated as the nugget diameter. In the case of different diameters, the average value of the long and short diameters was taken as the nugget diameter.
- As the current value of the continuous spot a weld lobe test was performed in advance under the same welding conditions, and a current value at which the nugget diameter was 6 mm was adopted. Under the above conditions, continuous hitting was performed up to the hitting point where the average nugget diameter was 3.8 mm or less.
- the hot stamped articles of the inventive examples are excellent in fatigue characteristics, spot weldability, and corrosion resistance.
- the hot stamped molded body of the comparative example includes “B” (defect) evaluation in evaluation items of fatigue characteristics, spot weldability, and corrosion resistance, and any of fatigue characteristics, spot weldability, and corrosion resistance is included. One or more were unsatisfactory.
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Abstract
Description
(1)鋼母材と、
前記鋼母材の表面に形成された金属層とを備えるホットスタンプ成形体であって、
前記金属層は、質量%で、Al:30.0~36.0%を含み、厚みが100nm~5μmであり、前記鋼母材との界面に位置する界面層と、MgZn2相と島状のFeAl2相が混在し、厚みが3μm~40μmであり、前記界面層の上に位置する主層とを備え、
前記金属層の平均組成が、質量%で、
Al:20.0~45.0%、
Fe:10.0~45.0%、
Mg:2.0~10.0%、
Sb:0~0.5%、
Pb:0~0.5%、
Cu:0~1.0%、
Sn:0~1.0%、
Ti:0~1.0%、
Ca:0~3.0%、
Sr:0~0.5%、
Cr:0~1.0%、
Ni:0~1.0%、
Mn:0~1.0%、
Si:0~1.0%、
残部:12.0~45.0%のZnおよび不純物であり、
前記主層において、前記MgZn2相が、質量%で、
Mg:13.0~20.0%、
Zn:70.0~87.0%、
Al:0~8.0%、
Fe:0~5.0%を含有し、
前記主層において、前記FeAl2相が、質量%で、
Al:40.0~55.0%、
Fe:40.0~55.0%、
Zn:0~15.0%を含有する、
ホットスタンプ成形体。
前記FeAl2相の体積分率が50.0~80.0%であり、
前記MgZn2相の体積分率が20.0~50.0%である、
上記(1)のホットスタンプ成形体。
前記FeAl2相の体積分率が60.0~75.0%であり、
前記MgZn2相の体積分率が25.0~45.0%である、
上記(1)または(2)のホットスタンプ成形体。
図4および図5を参照して、本実施形態に係るホットスタンプ成形体20の概要を説明する。図4および図5を参照して、本実施形態に係るホットスタンプ成形体20は、鋼母材(以下、単に「母材」ともいう。)1と、金属層3とを備え、金属層3は、母材1との界面に界面層31と、主層32とを備え、主層32は、MgZn2相32aと島状のFeAl2相32bが混在した状態のものとなる。金属層3の外面は、場合によって、酸化物層4が存在する。ただし、めっき層13の化学組成、特に、Zn、Mg成分の関係から、めっき鋼板表面全体にわたって、めっき断面において層状の酸化物は形成されにくい。よって、酸化物層4は、観察されても部分的にZn、Mg、Ca成分等の酸化物が微量に付着する程度である。また、この酸化物層4は、化成処理等の工程中のアルカリ処理によって取り除かれ、最終製品の表面には残存しない場合がある。
母材1は、本実施形態に係るホットスタンプ成形体20の用途に応じた特性を有しておれば、特に制約はない。母材1には、例えば、下記の化学組成を有する鋼を用いることができる。
炭素(C)は、ホットスタンプ成形体の強度を高めるのに有効な元素であるが、C含有量が多すぎると、ホットスタンプ成形体の靭性を低下させる。従って、C含有量は、0.05%~0.40%とする。好ましいC含有量の下限値は、0.10%であり、より好ましいC含有量の下限値は、0.13%である。好ましいC含有量の上限値は、0.35%である。
シリコン(Si)は、鋼を脱酸するのに有効な元素である。しかし、Si含有量が多すぎると、ホットスタンプの加熱中に鋼中のSiが拡散して、鋼板表面に酸化物を形成し、その結果、りん酸塩処理の効率を低下させる。また、Siは、鋼のAc3点を上昇させる元素である。このため、Siの過剰な含有は、鋼板のAc3点が上昇させて、ホットスタンプの加熱温度を上昇させるので、めっき層中のZnの蒸発が避けられなくなる。従って、Si含有量は、0.5%以下とする。好ましいSi含有量の上限値は、0.3%であり、より好ましいSi含有量の上限値は、0.2%である。好ましいSi含有量の下限値は、求められる脱酸レベルによって異なるが、通常、0.05%である。
マンガン(Mn)は、焼入れ性を高め、ホットスタンプ成形体の強度を高める。一方、Mnを過剰に含有させても、その効果は飽和する。従って、Mn含有量は、0.5%~2.5%とする。好ましいMn含有量の下限値は、0.6%であり、より好ましいMn含有量の下限値は、0.7%である。また、好ましいMn含有量の上限値は、2.4%であり、より好ましいMn含有量の下限値は、2.3%である。
りん(P)は、鋼中に含まれる不純物である。Pは結晶粒界に偏析して鋼の靭性を低下させ、耐遅れ破壊性を低下させる。従って、P含有量は、0.03%以下とする。P含有量は、できる限り少なくすることが好ましく、0.02%以下とするのが好ましい。P含有量の過剰な低減はコスト上昇を招くので、好ましい下限は0.01%である。
硫黄(S)は、鋼中に含まれる不純物である。Sは硫化物を形成して鋼の靭性を低下させ、耐遅れ破壊性を低下させる。従って、S含有量は0.01%以下とする。S含有量はできる限り少なくすることが好ましく、0.005%以下とするのが好ましい。S含有量の過剰な低減はコスト上昇を招くので、好ましい下限は0.0001%である。
アルミニウム(Al)は、鋼の脱酸に有効である。しかし、Alの過剰な含有は、鋼板のAc3点が上昇させて、ホットスタンプの加熱温度を上昇させるので、めっき層中のZnの蒸発が避けられなくなる。鋼のAc3点が上昇してホットスタンプ時の加熱温度がめっき層中のZnの蒸発温度を超えるおそれがある。従って、Al含有量は、0.1%以下とする。好ましいAl含有量の上限値は、0.05%であり、より好ましいAl含有量の下限値は、0.01%である。なお、本明細書において、Al含有量は、sol.Al(酸可溶Al)の含有量を意味する。
窒素(N)は、鋼中に不可避的に含まれる不純物である。Nは窒化物を形成して鋼の靭性を低下させる。Nは、鋼中にボロン(B)がさらに含有される場合、Bと結合することで固溶B量を減少させ、焼入れ性を低下させる。従って、N含有量は0.01%以下とする。N含有量はできる限り少なくすることが好ましく、0.005%以下とするのが好ましい。N含有量の過剰な低減はコスト上昇を招くので、好ましい下限は0.0001%である。
ボロン(B)は、鋼の焼入れ性を高め、ホットスタンプ後の鋼板の強度を高めるので、母材に含有させてもよい。しかし、Bを過剰に含有させても、その効果は飽和する。従って、B含有量は、0~0.005%とする。好ましいB含有量の下限値は0.0001%である。
チタン(Ti)は、窒素(N)と結合して窒化物を形成して、BN形成による焼入れ性の低下を抑制することができる。また、Tiは、ピン止め効果により、ホットスタンプの加熱時にオーステナイト粒径を微細化し、鋼板の靱性等を高めることができる。よって、Tiを母材に含有させてもよい。しかし、Tiを過剰に含有させても、上記効果は飽和し、しかも、Ti窒化物が過剰に析出すると、鋼の靭性を低下させる。従って、Ti含有量は、0~0.1%とする。好ましいTi含有量の下限値は、0.01%である。
クロム(Cr)は、鋼の焼入れ性を高めて、ホットスタンプ成形品の強度を高めるのに有効であるので、母材に含有させてもよい。しかし、Cr含有量が過剰であり、ホットスタンプの加熱時に溶解し難いCr炭化物が多量に形成されると、鋼のオーステナイト化が進行し難くなり、逆に焼き入れ性が低下する。従って、Cr含有量は、0~0.5%とする。また、好ましいCr含有量の下限値は0.1%である。
モリブデン(Mo)は、鋼の焼入れ性を高めので、母材に含有させてもよい。しかし、Moを過剰に含有させても、上記効果は飽和する。従って、Mo含有量は、0~0.5%とする。また、好ましいMo含有量の下限値は0.05%である。
ニオブ(Nb)は、炭化物を形成して、ホットスタンプ時に結晶粒を微細化し、鋼の靭性を高める元素であるので、母材に含有させてもよい。しかし、Nbを過剰に含有させると、上記効果は飽和し、さらに、焼入れ性を低下させる。従って、Nb含有量は、0~0.1%とする。好ましいNb含有量の下限値は0.02%である。
ニッケル(Ni)は、ホットスタンプの加熱時に、溶融Znに起因した脆化を抑制することができるので、母材に含有させてもよい。しかし、Niを過剰に含有させても、上記効果は飽和する。従って、Ni含有量は、0~1.0%とする。好ましいNi含有量の下限値は0.1%である。
(a)界面層31について
界面層31は、ホットスタンプの加熱によってめっき層中のAl成分が母材(地鉄)に拡散して、Feと結合した層のことであり、Fe-Al主体の金属間化合物(以下、単に「Fe-Al」ともいう。)で構成される。
図4および図5を参照して、主層32は、MgZn2相32aと島状のFeAl2相32bが混在した状態の層である。主層32は、ホットスタンプ時のスケール発生を抑制する効果を有し、かつ、ホットスタンプ成形体20の耐食性を担う。ホットスタンプ成形体20の耐食性は、主層32の犠牲防食により母材(地鉄)に赤錆を発生させないようにする作用と、主層32と、さらに上層の塗膜(図示省略)との密着性を確保し、錆範囲を拡張させない作用によって発揮される。
R=L/2d≧2
金属層3は、下記の平均組成を有する。
Alは、ホットスタンプ時の加熱によって、母材1および金属層3の界面付近では界面層31を形成して、主層32においてFeAl2相32bを生成することにより、Feが母材1から主層32中に過度に拡散するのを抑制するために必須の元素である。金属層3中のAl含有量が少なすぎると、界面層31の厚さが薄くなり、Feが母材1から主層32に拡散しやすくなり、MgZn2相32aに固溶するFe含有量が高くなる。また、主層32中のFeAl2相32bを減少させる。その結果、スポット溶接性の低下、LMEの発生、およびホットスタンプ時の溶着の発生につながる。よって、金属層3中のAl含有量の下限値は20.0%とする。
ホットスタンプ時に、めっき鋼板を加熱すると、Feが母材1から金属層3に拡散するため、ホットスタンプ成形体20の金属層3には必ずFeが含まれる。Feは、金属層3中のAlと結合して、界面層31および主層32中のFeAl2相32bを形成する。金属層3中のFe濃度は、界面層31の厚みが増大し、主層32中のFeAl2相32bの量が増大するほど上昇する。Fe濃度が低い場合、FeAl2相32bの量も減少するため、主層32の構造が崩れやすくなる。具体的には、Fe濃度が10.0%未満である場合、主層32中のMgZn2相32aの量が相対的に増加し、スポット溶接性、および溶着性が悪化する傾向にあるため、金属層3のFe含有量の下限は、10.0%とする。一方、Fe濃度が高すぎる場合、FeAl2相32bの量が多くなり、主層32中のMgZn2相32bが相対的に減少することで、主層32の構造が崩れて耐食性が悪化する傾向にあるため、金属層3のFe含有量の上限は、45.0%とする。金属層3のFe含有量の下限は、20.0%とするのが好ましく、27.0%とするのがより好ましく、32.5%とするのがさらに好ましい。金属層3のFe含有量の上限は、42.0%とするのが好ましく、36.5%とするのが好ましい。
Mgは、金属層3の耐食性を向上し、腐食試験における塗膜下の膨れ幅を改善するのに有効な元素である。また、Mgは、ホットスタンプの加熱時に、金属層3中のZn成分と結合して液相Znの発生を防止するので、LME割れを抑制する効果も有する。金属層3中のMg濃度が過度に低い場合、MgZn2相が形成されず、主層32中に固溶Znが残存するので、LMEが発生する可能性が増大する。そのため、Mg含有量は、2.0%以上とする。一方、金属層3中のMg含有量が多すぎると、過度に犠牲防食が働き、腐食試験において、塗膜膨れ幅、および流れ錆が急激に大きくなる傾向がある。よって、Mg含有量の上限は、10.0%とする。Mg含有量は、3.0%以上とするのが好ましく、3.5%以上とするのがより好ましい。
Pb:0~0.5%
Cu:0~1.0%
Sn:0~1.0%
Ti:0~1.0%
Sb、Pb、Cu、SnおよびTiは、金属層3中でZnと置換され、MgZn2相内で固溶体を形成するが、所定の含有量の範囲内であれば、ホットスタンプ成形体20に悪影響を及ぼさない。よって、これらの元素が金属層3に含まれていてもよい。しかし、それぞれの元素の含有量が過剰な場合、ホットスタンプの加熱時に、これらの元素の酸化物が析出し、ホットスタンプ成形体20の表面性状を悪化させ、りん酸化成処理が不良となって塗装後耐食性が悪化する傾向にある。また、腐食試験での赤錆発生までの時間も早くなる。また、Pb、Snの含有量が過剰な場合には、溶着性およびLME性を劣化させる。SbおよびPbの含有量は、0.5%以下、Cu、SnおよびTiの含有量は1.0%以下とする。SbおよびPbの含有量は0.2%以下とするのが好ましく、Cu、SnおよびTiの含有量は、0.8%以下が好ましく、0.5%以下がより好ましい。
Sr:0~0.5%
CaおよびSrは、製造時にめっき浴上に形成されるトップドロスの生成を抑制することができる。また、CaおよびSrは、ホットスタンプの熱処理時に、大気酸化を抑制する傾向があるため、熱処理後のめっき鋼板の色変化を抑制することができる。これらの効果は、CaよりもSrの方が強いため、Srのほうが少量で効果を発揮する。また、これらの元素の含有量が過剰な場合、腐食試験において塗膜膨れ幅および流れ錆に悪影響を与える。よって、CaおよびSrから選択される一種以上を、Ca含有量は3.0%以下、Sr含有量は0.5%以下の範囲で、金属層3に含有させてもよい。Ca含有量は、2.0%以下とするのが好ましく、1.5%以下とするのがより好ましい。Sr含有量は、0.3%以下とするのが好ましく、0.1%以下とするのがより好ましい。上記の効果を得るためには、Ca含有量は0.1%以上とするのが好ましく、Sr含有量は0.05%以上とするのが好ましい。
Ni:0~1.0%
Mn:0~1.0%
Cr、NiおよびMnは、めっき鋼板においては、めっき層と母材との界面付近に濃化し、めっき層表面のスパングルを消失させるなどの効果を有する。これらの元素は、ホットスタンプ成形体20の金属層3中では、Feと置換され、界面層31中に含まれるか、主層32中のFeAl2相32b中で固溶体を形成する。よって、Cr、NiおよびMnから選択される一種以上が、金属層3中に含まれていてもよい。しかし、これらの元素の含有量が過剰な場合には、塗膜膨れ幅および流れ錆が大きくなり、耐食性が悪化する傾向にある。よって、Cr、NiおよびMnの含有量は、それぞれ1.0%以下とする。Cr、NiおよびMnの含有量は、0.5%とするのが好ましく、0.1%以下とするのがより好ましい。Cr、NiおよびMnの含有量の下限は、0.01%とするのが好ましい。
Siは、溶融状態のZnおよびAlの活量を大きく下げ、ホットスタンプ時におけるFeおよび金属層3を構成する元素の拡散に大きく影響を与える元素である。したがって、Siは、FeAl2相32bの分散構造を大きく崩しかねないため、適切な含有量に制限する必要がある。金属層3中のSi含有量が過剰な場合、金属層3中のMgZn2相32aが減少して、母材と金属層との界面を起点にMg2Si相が形成され、耐食性が大きく悪化する。また、MgZn2相の減少によって、フリーとなったZnがZn相を形成するため、LMEが発生することがある。さらに、Siは、金属層3内部へのFeの拡散を抑制し、界面層31の成長およびFeAl2相32bの成長を阻害する。このため、Si含有量は、極力低減するのが好ましく、1.0%以下とする。Si含有量は、0.2%以下とするのが好ましく、より好ましいのは0%である。
金属層3中において、防錆の観点からZnの含有は必須である。金属層3中に含まれるZn成分のほとんどは、MgZn2相32aとして存在している。一方、Zn原子はAl原子と置換することが可能であるから、Znは、少量ではあるが、FeAl2相32bにも固溶することが可能である。従って、金属層中に含まれるMgZn2相32aの量が増大した場合、金属層3中のZn濃度も増大する。
本実施形態に係るホットスタンプ成形体20の最表層には、めっき成分の酸化によって酸化物層4が形成される場合がある。酸化物層4は、ホットスタンプ後に供されるりん酸化成処理性および電着塗装性を悪化させる恐れがあるので、薄い方がよい。1.0μm以下の厚みであれば、金属層3の主たる性能に影響を与えない。
本実施形態に係るホットスタンプ成形体20を得るために用いるめっき鋼板10について説明する。図3を参照して、本実施形態に係るホットスタンプ成形体20を得るために用いるめっき鋼板10は、母材(地鉄)11とめっき層13との間に拡散層12を備える。母材11の化学組成は、本実施形態に係るホットスタンプ成形体20の母材1の化学組成と共通するので、説明を省略する。拡散層12は、Fe2(Al,Zn)を主体とする薄い層である。めっき層13は、Zn-Al-Mg系めっき層であり、ホットスタンプ後に上述した化学組成を有する金属層3を形成するものであれば特に制約がない。めっき層13としては、例えば、下記の化学組成を有するものを用いることができる。
Znは、本実施形態に係るホットスタンプ成形体20の主層32にMgZn2相32aを形成するために必須の元素であり、その含有量は、17.0%以上とすることが推奨される。
Alは、本実施形態に係るホットスタンプ成形体20の主層32に島状のFeAl2相32bを形成するために必須の元素であり、その含有量は、10.0~70.0%とすることが推奨される。
Mgは、本実施形態に係るホットスタンプ成形体20の主層32にMgZn2相32aを形成するために必須の元素であり、その含有量は、7.0~20.0%とすることが推奨される。この範囲のMgは、溶融状態にあるZn、Al、または、ZnおよびAlの混合物と、地鉄との過度の反応を抑制する。
Feは、ホットスタンプの加熱中に島状のFeAl2相を析出するために、その含有量は0.05%以上とすることが推奨される。一方、ホットスタンプ時の過度な合金化反応を抑制するために、Feの含有量は、2.0%以下が好ましい。めっき層中のFeは、めっき浴中に含まれていたものだけでなく、母材由来のものも含まれる。
Siは、その含有量が多すぎると、ホットスタンプ時にMgと反応してMg2Si相を形成し、耐食性が大きく悪化する。よって、その含有量は1.0%以下が好ましい。
Sb:0~0.5%
Pb:0~0.5%
Cu:0~1.0%
Sn:0~1.0%
Ti:0~1.0%
Ca:0~3.0%
Sr:0~0.5%
Cr:0~1.0%
Ni:0~1.0%
Mn:0~1.0%
次に、本実施形態に係るホットスタンプ成形体20の製造方法について説明する。本実施形態に係るホットスタンプ成形体の製造方法は、母材を準備する工程(母材準備工程)と、母材にZn-Al-Mgめっき層を形成してめっき鋼板を準備する工程(めっき処理工程)と、めっき鋼板に対してホットスタンプを行う工程(熱間プレス工程)と、を含み、必要に応じて防錆油膜形成工程、及びブランキング加工工程を含む。以下、各工程を詳述する。
本工程は、母材を準備する工程である。例えば、上述した化学組成を有する溶鋼を製造し、製造された溶鋼を用いて、鋳造法によりスラブを製造する。または、製造された溶鋼を用いて、造塊法によりインゴットを製造してもよい。さらに、製造されたスラブ又はインゴットを熱間圧延することで母材(熱延板)を製造する。なお、必要に応じて、上記熱延板に対して酸洗処理を行った後、熱延板に対して冷間圧延を行い、冷延板を母材として用いてもよい。
本工程は、母材にZn-Al-Mgめっき層を形成する工程である。本工程では、前述した組成のZn-Al-Mgめっき層を母材の両面に形成する。めっき層の付着量は、片面当たり170.0g/m2以下とすることが好ましい。なお、本工程では、めっき付着の補助として、Niプレめっき、Snプレめっき等の各種プレめっきを施すことも可能であるが、各種プレめっきは、合金化反応に変化を及ぼすため、プレめっきの付着量は、片面当たり2.0g/m2以下とすることが好ましい。
本工程は、上述のめっき鋼板に対して、緩加熱した後、ホットスタンプを行う工程である。本工程では、主に通電加熱(ジュール熱)、または輻射熱を利用してめっき鋼板を加熱する。
本工程は、めっき処理工程後、かつ、ホットスタンプ工程前に、ホットスタンプ用のめっき鋼板の表面に防錆油を塗布して防錆油膜を形成する工程である。ホットスタンプ用のめっき鋼板が製造されてからホットスタンプが行われるまでに、長期間が経過している場合、めっき鋼板の表面が酸化するおそれがある。しかし、本工程により防錆油膜が形成されためっき鋼板の表面は酸化し難く、これにより、スケールの形成が抑制される。なお、防錆油膜の形成方法は、公知の技術を適宜用いることができる。
本工程は、防錆油膜形成工程後、かつ、ホットスタンプ工程前に、ホットスタンプ用のめっき鋼板に対して剪断加工または打ち抜き加工の少なくともいずれかを行って、めっき鋼板を特定の形状に加工する工程である。ブランキング加工後のめっき鋼板の剪断面は酸化し易いが、上述した防錆油膜形成工程によって、めっき鋼板表面に事前に防錆油膜が形成されていれば、めっき鋼板の剪断面にも防錆油がある程度広がることにより、ブランキング加工後のめっき鋼板の酸化を抑制することができる。
次に、本実施形態に係るホットスタンプ成形体における金属層の解析方法について説明する。
(1)上記のとおり、FeAl2相の面積率の測定と同様にして、主層32中において全輪郭線が認識できるFeAl2相32bをSEMの反射電子像から認識した。このとき、FeAl2相の面積から算出した円相当径が100nm以上のものを測定対象とした。100nm未満のFeAl2相は、性能に実質的な影響を与えないので無視した。
(2)FeAl2相32bを金属層と母材との界面に投影した長さ2d、FeAl2相の輪郭線(周囲長さ)Lを測定した。なお、隣接する複数の島状FeAl2相が凝集している場合には、凝集体を構成する、それぞれのFeAl2相の2dおよびLを測定した。
(3)そして、測定した2dとLを式R=L/2dに当てはめてR値を算出した。
(4)上記のとおり、FeAl2相32の面積率の測定と同様に、少なくとも5断面(5視野)以上のSEMの反射電子像から、1断面につき5個以上で合計50個以上のFeAl2相32bのR値を測定した。そして、測定したR値の平均を主層32中に占めるFeAl2相32のR値とした。
(5)R=2.0以上のとき、FeAl2相32bは島状であるとした。一方で、FeAl2相32bが2.0未満のとき、FeAl2相32bは層状であるとした。FeAl2相32bが2.0未満のとき、FeAl2相32bは従来のホットスタンプ成形体とほぼ同じ状態であり、R値の測定に使用できるFeAl2相32bは非常に少なかった。
LME性を調べるため、ホットスタンプ前のめっき鋼板(50mm×50mm×1.4mm)を加熱炉に装入して900℃に加熱した。なお、加熱炉の炉温は、鋼板のAc3点以上の温度である900℃に設定した。
次いで、ホットスタンプ成形体(板状100×50mm)に対して、日本パーカライジング株式会社製の表面調整処理剤(商品名:プレパレンX)を用いて、表面調整を室温で20秒間行った。次いで、表面調整後のホットスタンプ成形体に対して、日本パーカライジング株式会社製のりん酸亜鉛処理液(商品名:パルボンド3020)を用いて、りん酸塩処理を行った。具体的には、処理液の温度を43℃とし、ホットスタンプ成形体を処理液に120秒間浸漬した。これにより、ホットスタンプ成形体の鋼板表面にりん酸塩被膜を形成した。
次いで、ホットスタンプ成形体の連続打点性を確認するため、ホットスタンプ成形体において主層厚みが25μmとなるサンプル(0.8mm板)を準備した。
11 母材
12a 拡散層
13aめっき層
20 本実施形態に係るホットスタンプ成形体
1 鋼母材(母材)
3 金属層
31 界面層
32 主層
32a MgZn2相
32b FeAl2相
4 酸化物層
10a 通常の条件で製造しためっき鋼板
11a 母材
12a 拡散層
13aめっき層
20a 通常のホットスタンプ成形体
1a 母材
2a 表層部
21a 界面層
21b 金属層
4a 酸化物層
Claims (3)
- 鋼母材と、
前記鋼母材の表面に形成された金属層とを備えるホットスタンプ成形体であって、
前記金属層は、質量%で、Al:30.0~36.0%を含み、厚みが100nm~5μmであり、前記鋼母材との界面に位置する界面層と、MgZn2相と島状のFeAl2相が混在し、厚みが3μm~40μmであり、前記界面層の上に位置する主層とを備え、
前記金属層の平均組成が、質量%で、
Al:20.0~45.0%、
Fe:10.0~45.0%、
Mg:2.0~10.0%、
Sb:0~0.5%、
Pb:0~0.5%、
Cu:0~1.0%、
Sn:0~1.0%、
Ti:0~1.0%、
Ca:0~3.0%、
Sr:0~0.5%、
Cr:0~1.0%、
Ni:0~1.0%、
Mn:0~1.0%、
Si:0~1.0%、
残部:12.0~45.0%のZnおよび不純物であり、
前記主層において、前記MgZn2相が、質量%で、
Mg:13.0~20.0%、
Zn:70.0~87.0%、
Al:0~8.0%、
Fe:0~5.0%を含有し、
前記主層において、前記FeAl2相が、質量%で、
Al:40.0~55.0%、
Fe:40.0~55.0%、
Zn:0~15.0%を含有する、
ホットスタンプ成形体。 - 前記主層において、
前記FeAl2相の体積分率が50.0~80.0%であり、
前記MgZn2相の体積分率が20.0~50.0%である、
請求項1に記載のホットスタンプ成形体。 - 前記主層において、
前記FeAl2相の体積分率が60.0~75.0%であり、
前記MgZn2相の体積分率が25.0~45.0%である、
請求項1または2に記載のホットスタンプ成形体。
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US (1) | US11338550B2 (ja) |
EP (1) | EP3770297B1 (ja) |
JP (1) | JP6443596B1 (ja) |
KR (1) | KR102425232B1 (ja) |
CN (1) | CN111868290B (ja) |
MX (1) | MX2020009684A (ja) |
WO (1) | WO2019180852A1 (ja) |
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JPWO2021171514A1 (ja) * | 2020-02-27 | 2021-09-02 | ||
JPWO2021171519A1 (ja) * | 2020-02-27 | 2021-09-02 | ||
WO2021171515A1 (ja) * | 2020-02-27 | 2021-09-02 | 日本製鉄株式会社 | ホットスタンプ成形体 |
KR20210135578A (ko) * | 2019-04-19 | 2021-11-15 | 닛폰세이테츠 가부시키가이샤 | 도금 강판 |
JPWO2020213680A1 (ja) * | 2019-04-19 | 2021-12-23 | 日本製鉄株式会社 | めっき鋼材 |
EP3957765A4 (en) * | 2019-04-19 | 2022-08-24 | Nippon Steel Corporation | PLATED STEEL SHEET |
JP7243949B1 (ja) * | 2021-10-29 | 2023-03-22 | Jfeスチール株式会社 | 熱間プレス部材 |
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WO2023163075A1 (ja) * | 2022-02-22 | 2023-08-31 | 日本製鉄株式会社 | めっき鋼材 |
JP7440771B2 (ja) | 2020-08-31 | 2024-02-29 | 日本製鉄株式会社 | ホットスタンプ成形体 |
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CN112143949B (zh) * | 2019-06-27 | 2021-12-07 | 比亚迪股份有限公司 | 一种压铸铝合金及其制备方法和应用 |
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WO2021039973A1 (ja) * | 2019-08-29 | 2021-03-04 | 日本製鉄株式会社 | ホットスタンプ成形体 |
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Also Published As
Publication number | Publication date |
---|---|
MX2020009684A (es) | 2020-10-12 |
CN111868290A (zh) | 2020-10-30 |
JP6443596B1 (ja) | 2018-12-26 |
JPWO2019180852A1 (ja) | 2020-04-23 |
US11338550B2 (en) | 2022-05-24 |
EP3770297A1 (en) | 2021-01-27 |
EP3770297B1 (en) | 2022-06-01 |
KR20200135437A (ko) | 2020-12-02 |
CN111868290B (zh) | 2022-05-31 |
US20210039354A1 (en) | 2021-02-11 |
EP3770297A4 (en) | 2021-08-25 |
KR102425232B1 (ko) | 2022-07-27 |
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