JPH01319661A - Alloying hot dip galvanized steel sheet excellent in press formability - Google Patents
Alloying hot dip galvanized steel sheet excellent in press formabilityInfo
- Publication number
- JPH01319661A JPH01319661A JP63152685A JP15268588A JPH01319661A JP H01319661 A JPH01319661 A JP H01319661A JP 63152685 A JP63152685 A JP 63152685A JP 15268588 A JP15268588 A JP 15268588A JP H01319661 A JPH01319661 A JP H01319661A
- Authority
- JP
- Japan
- Prior art keywords
- steel sheet
- layer
- phase
- dip galvanized
- press formability
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229910001335 Galvanized steel Inorganic materials 0.000 title claims description 11
- 239000008397 galvanized steel Substances 0.000 title claims description 11
- 238000005275 alloying Methods 0.000 title abstract description 8
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 44
- 239000010959 steel Substances 0.000 claims abstract description 44
- 238000007747 plating Methods 0.000 claims abstract description 31
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 22
- 239000000956 alloy Substances 0.000 claims abstract description 22
- 229910001297 Zn alloy Inorganic materials 0.000 claims abstract description 3
- 229910052742 iron Inorganic materials 0.000 claims description 18
- 229910052725 zinc Inorganic materials 0.000 claims description 6
- 229910052745 lead Inorganic materials 0.000 claims description 4
- 229910052796 boron Inorganic materials 0.000 claims description 3
- 229910052750 molybdenum Inorganic materials 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 229910052702 rhenium Inorganic materials 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 229910052718 tin Inorganic materials 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 229910052721 tungsten Inorganic materials 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 229910052748 manganese Inorganic materials 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- 239000000463 material Substances 0.000 abstract description 12
- 238000000227 grinding Methods 0.000 abstract description 11
- 239000011248 coating agent Substances 0.000 abstract description 4
- 238000000576 coating method Methods 0.000 abstract description 4
- 238000005246 galvanizing Methods 0.000 abstract description 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 abstract 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 30
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 11
- 239000011701 zinc Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 5
- 238000005096 rolling process Methods 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000009864 tensile test Methods 0.000 description 4
- 239000010960 cold rolled steel Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000004070 electrodeposition Methods 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 230000003746 surface roughness Effects 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000009713 electroplating Methods 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 229920000298 Cellophane Polymers 0.000 description 1
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 1
- 229910001096 P alloy Inorganic materials 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 238000001479 atomic absorption spectroscopy Methods 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/26—After-treatment
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Coating With Molten Metal (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、自動車、建材等にプレス成形および塗装を行
って用いられる合金化溶融亜鉛めっき鋼板に関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to an alloyed hot-dip galvanized steel sheet used for press forming and painting for automobiles, building materials, etc.
(従来の技術)
合金化溶融亜鉛めっき鋼板(以下、GA錆鋼板記す。)
は、そのBEれたi1食・1生のため、自動車外板等の
高い防錆性を要求される用途に用いられている。(Prior art) Alloyed hot-dip galvanized steel sheet (hereinafter referred to as GA rust steel sheet)
Because it has a BE of 1 serving and 1 serving, it is used in applications that require high rust prevention properties such as automobile exterior panels.
従来のG A i[板は、GA鋼板プレス時の圧縮変形
によって生じるパウタリングと呼はれるめっき層の粉化
fll 1811を避けるために、溶融亜鉛めっぎ後の
加熱による合金化工程での条件をコントロールして、合
金化溶融亜鉛めっき層(以下、GA層と記す。)中のF
e 9Q度を低くしている。Conventional G A i [sheets are made using the conditions in the alloying process by heating after hot-dip galvanizing to avoid powdering of the plating layer called powdering caused by compressive deformation during pressing of GA steel sheets. F in the alloyed hot-dip galvanized layer (hereinafter referred to as GA layer)
e 9Q degree is lowered.
一方、GA層表面の合金組成、組織に基つく別の問題、
taであるGA錆鋼板電着塗装する際に発生するクレー
タ−の低減と塗装後の二次密着・[1の改善のために、
合金化後のGA層表面に純Zn相(η相)か残存しない
ように合金化する方法や、特公昭58 15554号公
報に開示されたF e−Z n 系合金めっき、特開昭
61−253397号公報に開示さねたFe−P系合金
めっき等か知られている。 しかし、このような処理
のプレス成形性への影響やその改善に好適な条件を開示
したものはなく、依然としてGA錆鋼板プレス成形性の
向上は図らねでいない。On the other hand, another problem is based on the alloy composition and structure of the GA layer surface.
To reduce craters that occur when electrocoating GA rust steel sheets and improve secondary adhesion after painting, [1]
A method of alloying so that no pure Zn phase (η phase) remains on the surface of the GA layer after alloying, Fe-Zn alloy plating disclosed in Japanese Patent Publication No. 58-15554, Japanese Patent Application Laid-open No. 1983-15554, Fe--P alloy plating disclosed in Japanese Patent No. 253397 is known. However, nothing has disclosed the influence of such treatment on press formability or the conditions suitable for its improvement, and no attempt has yet been made to improve the press formability of GA rusted steel sheets.
(発明か解決しようとする;I!I!題)プレス成形に
用いられるGA錆鋼板は、GA層の過度の合金化によっ
てF e / G A層界面に生しる硬くて脆い「相(
Fe32n+o相)の形成を抑制し、削パウタリング・
袖を付与するために、GA層中のFeン農度を低くして
いる。 しかし、このようなGA錆鋼板実際に自動車
外板用にプレスするに至り、プレス成形性か問題となっ
た。 即ち、耐バウタリング性改善のためにGA層のF
e濃度を低くしたところ、GA層表面にはζ相(reZ
n+3相)あるいはη相(Zn相)か残存した。 これ
らの相は柔かいため、GA錆鋼板プレス成形時おいて、
ヒート部のめつぎ表面の変形か大きくなり、その結果、
摺動抵抗か高くなり、鋼板の流入か困知となり、母オΔ
鋼板は十分な落首を備えているにもかかわらず、板厚の
極端に薄いくびれ部の出来るネッキング現象や割れか発
生しやすくなった。(Invention or attempt to solve; I!I! Problem) GA rusted steel sheets used for press forming have a hard and brittle "phase" produced at the Fe/GA layer interface due to excessive alloying of the GA layer.
Suppresses the formation of Fe32n+o phase) and reduces powdering and
In order to provide sleeves, the Fe content in the GA layer is lowered. However, when such GA rusted steel sheets were actually pressed into automobile exterior panels, the press formability became a problem. That is, in order to improve the buttering resistance, F of the GA layer is
When the e concentration was lowered, the ζ phase (reZ
n+3 phase) or η phase (Zn phase) remained. Since these phases are soft, during press forming of GA rust steel sheet,
The deformation of the matte surface of the heated part becomes large, and as a result,
The sliding resistance becomes high, and it becomes difficult to know whether the steel plate will flow in, and the mother plate ∆
Although steel plates have a sufficient neck drop, they are prone to necking and cracking due to the extremely thin constrictions of the plate.
上記事実に鑑み、本発明は、通常GA鋼板の耐クレータ
一対策として行われているFe系合金めつきのプレス成
形性への影響の検討から、従来技術ては達成し得ながっ
た耐バツクリング性か高いにもかかわらずプレス成形(
深絞り加工)時にネッキング現象や割れか発生せず、G
A錆鋼板母材の材料特性とおりにプレス加工可能なGA
錆鋼板見出し、その提供を目的とするものである。In view of the above facts, the present invention has been developed based on a study of the effect of Fe-based alloy plating, which is usually carried out as a measure against cratering in GA steel sheets, on press formability, and has been developed to provide buckling resistance that has not been achieved with conventional techniques. Despite its high durability, press molding (
G
A: GA that can be pressed according to the material properties of the rusted steel plate base material
The purpose of this article is to provide information on rusted steel plates.
(課題を解決するだめの手段)
GA層の表面は、特に表面かζ相あるいはη相である場
合には、これらの相か柔らかいために、プレス時に型に
押し付けられて変形し、その摺動面積か増加し、時には
ゴーリングか起こるために摺動抵抗か高くなる。 GA
錆鋼板プレス成形性を母材の材料特性とおりの十分なも
のにするには、GA層表面の摺動性を向上させ、プレス
時の鋼板流人を阻害させないことか重要である。(Means to Solve the Problem) The surface of the GA layer, especially when the surface is in the ζ phase or η phase, is soft and deforms when pressed against the mold during pressing, causing its sliding. The sliding resistance increases as the area increases and sometimes galling occurs. G.A.
In order to achieve sufficient press formability of a rusted steel sheet in accordance with the material properties of the base material, it is important to improve the sliding properties of the GA layer surface so as not to impede the flow of the steel sheet during pressing.
この解決手段として、GA層表面に薄く硬い層を形成し
、ζ相の変形による摺動面積の増加やゴーリングの発生
を抑制すねはよいと考え、電解鉄およびその合金の硬度
か高いことに着目し、ζ相上に適量のFe系電気めっき
を行うことに思い至り、本発明に至った。As a means of solving this problem, we thought it would be a good idea to form a thin, hard layer on the surface of the GA layer to suppress the increase in sliding area and the occurrence of galling due to the deformation of the ζ phase, and focused on the high hardness of electrolytic iron and its alloys. However, we came up with the idea of performing an appropriate amount of Fe-based electroplating on the ζ phase, leading to the present invention.
本発明は、鋼板の少なくとも一方の面上に、Fe−Zn
合金より成る合金化溶融亜鉛めっき層を有し、該合金化
溶融亜鉛めっき層上に、ビッカース硬度400以上のF
eまたはFe系合金めっき層を有することを特徴とする
プレス成形性に優れる合金化溶融亜鉛めっき鋼板を提供
するものである。The present invention provides Fe-Zn on at least one surface of a steel plate.
It has an alloyed hot-dip galvanized layer made of an alloy, and on the alloyed hot-dip galvanized layer is an F having a Vickers hardness of 400 or more.
The present invention provides an alloyed hot-dip galvanized steel sheet having excellent press formability and having an e- or Fe-based alloy plating layer.
FeまたはFe系の合金めっき層の付着量は、2 g
/ m’以上10 g/ m”以下であることか好まし
い。The amount of deposited Fe or Fe-based alloy plating layer is 2 g.
/m' or more and 10 g/m'' or less.
合金化溶融亜鉛めっき層は、好ましくは、δx相、ζ相
およびη相の混相、さらに好ましくはδx相およびζ相
の混相であるのがよい。The alloyed hot-dip galvanized layer is preferably a mixed phase of a δx phase, a ζ phase and a η phase, more preferably a mixed phase of a δx phase and a ζ phase.
Fe系合金めつキ層は、B、P、S、、Ti、■、Cr
、Mn、Co、Ni、Zn、Mo。The Fe-based alloy plating layer is made of B, P, S, Ti, ■, Cr.
, Mn, Co, Ni, Zn, Mo.
S n、W、Re、、Pdのうぢより選はれた1種また
は2種以上の元素を含有して成る層であることか好まし
い。Preferably, the layer contains one or more elements selected from Sn, W, Re, and Pd.
以下に、本発明のプレス成形性に(量れる合金化溶融亜
鉛めっき鋼板について、詳細に説明する。Below, the alloyed hot-dip galvanized steel sheet that can be evaluated for press formability according to the present invention will be described in detail.
本発明のプレス成形性に(f]する合金化溶融亜鉛めっ
き鋼板(す、鋼板の少なくとも一方の面十に、Fe−Z
n合金より成る合金化溶融亜鉛めっき層を有し、その層
」−には、FeまたはFe系合金めっき層を有するか、
FeまたはFe系合金めっき層の硬度は、Fe単相と同
等あるいはそれ以上のものであること、ビッカース硬度
で表現すると、ζ相150〜200に対して400以上
であることか重要である。Alloyed hot-dip galvanized steel sheet (f) that improves the press formability of the present invention (Fe-Z
It has an alloyed hot-dip galvanized layer made of an n-alloy, and that layer has an Fe or Fe-based alloy plating layer, or
It is important that the hardness of the Fe or Fe-based alloy plating layer be equal to or higher than that of single phase Fe, and expressed in terms of Vickers hardness, be 400 or more for the ζ phase of 150 to 200.
その理由は、FeまたはFe系合金めっき層か柔らかい
と、GA錆鋼板プレス成形時おりるネッキング現象や割
れの発生を防止てきないからである。The reason for this is that if the Fe or Fe-based alloy plating layer is soft, it will not be possible to prevent the occurrence of necking or cracking that occurs during press forming of GA rusted steel sheets.
また、この「eまたはFe系合金めっき層のGA錆鋼板
のイ=J着量は、少くとも一方のGA層表面に2 g
/ m’以上10 g/ m’以下であることか好まし
い。In addition, the amount of deposit of GA rust steel plate with ``e'' or Fe-based alloy plating layer is 2 g on at least one GA layer surface.
/m' or more and 10 g/m' or less.
GA層表面は微細な凹凸に富むため、付着量か2 g/
m’未満であると、FeあるいはFe系の合金めっき
でGA錆鋼板表面を十分に覆うことかできない。 また
、10 g/ m’超であると、高硬度なFeあるいは
f’e系の合金めつぎ層の膜か形成され、この膜かGA
錆鋼板プレス成形時変形に追従てきないためにフレーク
状にヱリ離してしまい、好ましくない。Since the surface of the GA layer is rich in fine irregularities, the amount of adhesion is approximately 2 g/
If it is less than m', the surface of the GA rusted steel sheet cannot be sufficiently covered with Fe or Fe-based alloy plating. Moreover, if it exceeds 10 g/m', a film of a high hardness Fe or f'e alloy patch layer is formed, and this film is
Since the rusted steel plate cannot follow the deformation during press forming, it flakes off, which is undesirable.
GA層の形成、即ち素地鋼板から亜鉛めっき層内へFe
を拡散させて合金化させる際は、GA層は、好ましくは
δx相、ζ相およびη相の混相、さらに好ましくはδx
相およびζ相の混相となるよう制御する。Formation of GA layer, i.e. Fe from the base steel sheet into the galvanized layer.
When alloying by diffusion, the GA layer is preferably a mixed phase of δx phase, ζ phase and η phase, more preferably δx phase.
Control is performed to create a mixed phase of phase and ζ phase.
GA層をこのように規定する理由は、プレス成形時にめ
っき層の剥離(すなわちパウダリング)を発生させない
ためである。 また、塗装後の二次密着性を良好とす
るためである。The reason why the GA layer is defined in this manner is to prevent peeling of the plating layer (ie, powdering) during press molding. This is also to improve secondary adhesion after coating.
さらに、Fe系合金めっき層は、B、P、S 、
Ti 、 V 、 Cr、 Mn V
Co、 Ni。Furthermore, the Fe-based alloy plating layer contains B, P, S,
Ti, V, Cr, MnV
Co, Ni.
Zn、Mo、Sn、W、Re、Pbのうちより選はれた
1種または2種以上の元素を含有するものであることか
好ましい。Preferably, it contains one or more elements selected from Zn, Mo, Sn, W, Re, and Pb.
その理由は、このような元素は、耐クレーター性に好ま
しい効果を発揮するものであると共に、ビッカース硬度
400以上のめつき層を、安定に電析せしめる働ぎをも
つためである。This is because such elements have a favorable effect on crater resistance and also have the function of stably depositing a plating layer having a Vickers hardness of 400 or more.
また、Fe系合金めっき層は、これらの元素の他にシリ
カ、アルミナ等を分散させた分散めっきとすると、塗料
密着性等か向上するのでり了ましい。Further, it is preferable to use dispersion plating in which silica, alumina, etc. are dispersed in addition to these elements for the Fe-based alloy plating layer, since this improves paint adhesion.
以下に、本発明のプレス成形性に優れる合金化溶融亜鉛
めっぎ鋼板の好適製造方法を示す。Below, a preferred method for manufacturing the alloyed hot-dip galvanized steel sheet of the present invention having excellent press formability will be described.
冷延鋼板は、再結晶か十分に起こり、良好なプレス成形
性を得るのに必要な温度、具体的には700〜880℃
の範囲の温度で焼鈍された後、冷却過程て430〜50
0℃程度の温度に保持された溶融亜鉛浴に浸漬され、め
っきされ、ガスワイピングにより所定の亜鉛付着屋とさ
れた後、450〜600℃の温度に加熱保持される。
この操作により素地鋼板から亜鉛めっき層内へFeか拡
散し、合金化する。 続いて、めっき処理を施された冷
延鋼板は冷却され、02〜2%の圧下率て調質圧延され
る。Cold-rolled steel sheets must be heated at a temperature required to sufficiently undergo recrystallization and obtain good press formability, specifically 700 to 880°C.
After being annealed at a temperature in the range of 430-50
After being immersed in a molten zinc bath maintained at a temperature of about 0°C, plated, and made into a predetermined zinc adhesion chamber by gas wiping, it is heated and maintained at a temperature of 450 to 600°C.
Through this operation, Fe is diffused from the base steel sheet into the galvanized layer and alloyed. Subsequently, the plated cold-rolled steel sheet is cooled and temper-rolled at a rolling reduction of 0.2 to 2%.
この調質圧延により、表面粗さは5Ra−13〜2.2
μm程度(圧延前)から07〜14μm (圧延後)ま
で小さくなる。Through this temper rolling, the surface roughness is 5Ra-13 to 2.2
It becomes smaller from about μm (before rolling) to 07 to 14 μm (after rolling).
調質圧延後のGA層板は、最後に、電気めっき法により
FeまたはFe系合金めっきか施される。The GA laminate after temper rolling is finally plated with Fe or Fe-based alloy by electroplating.
(実施例) 次に、本発明を実施例に基いて説明する。(Example) Next, the present invention will be explained based on examples.
本発明のGA錆鋼板よび従来のGA錆鋼板作り、めっき
性状を評価し、オΔ料特性を試験・評価した。The GA rusted steel sheet of the present invention and the conventional GA rusted steel sheet were manufactured, the plating properties were evaluated, and the properties of the Δ material were tested and evaluated.
母材鋼板は、いずれも板厚0 7mmの超低炭素鋼(C
: 0.002〜0.004重量%)を使用し、〒(ラ
ンクフォート)値を増減させるために、焼鈍条件、母材
鋼板への添加成分とその含イj量を若干変化させた。
表2には、母材鋼板へ添加した成分とその含有量の範囲
を示し、表3には、各鋼板の第1料特性値の範囲を示し
た。The base steel plates are all ultra-low carbon steel (C
: 0.002 to 0.004% by weight), and in order to increase or decrease the (Lankfort) value, the annealing conditions, the components added to the base steel sheet, and their content were slightly changed.
Table 2 shows the components added to the base steel sheet and the range of their content, and Table 3 shows the range of the first material characteristic values of each steel sheet.
表4には、下記の方法で試験・評価した各鋼板のめフき
性状とオオ料特性の試験結果を示した。 また、第1図
には、引張試験におりる〒(ランクフォーF )値と平
底円筒絞り試験におりる限界絞り比(L、D、R)との
関係を示した。Table 4 shows the test results for the polishing properties and coating properties of each steel plate tested and evaluated by the following methods. Further, FIG. 1 shows the relationship between the 〒 (Rank Four F) value obtained in the tensile test and the critical drawing ratio (L, D, R) obtained in the flat bottom cylindrical drawing test.
めっき性状は、GA層目付量、GA層Fe濃度、GA層
の相構成、上層めっきの成分組成、上層めっき目付量、
表面粗さについて記した。The plating properties include the GA layer basis weight, GA layer Fe concentration, GA layer phase composition, upper layer plating component composition, upper layer plating basis weight,
The surface roughness was described.
評価条件は、以下の通りである。The evaluation conditions are as follows.
GA層層目骨量およびGA層Fe濃度は、上層めっきを
行う前の時点て、Feの電位まてめつきを電気熔解し、
溶出したZn、Fe量を、原子吸光分析法により測定し
て得た。The bone mass of the GA layer and the Fe concentration of the GA layer are determined by electrolyzing the Fe potential and plating before performing the upper layer plating.
The amounts of eluted Zn and Fe were measured by atomic absorption spectrometry.
GA層の相構成は、定電流でGA層を溶解した時の電位
変化より求めた。The phase structure of the GA layer was determined from the potential change when the GA layer was dissolved with a constant current.
−F層めっき目イ]量は、上層めっき前後の重量差より
求め、成分組成は、エネルギー分散型X線分析装置(E
DX)で分析した。- The amount of F layer plating is determined from the difference in weight before and after the upper layer plating, and the component composition is determined using an energy dispersive X-ray analyzer (E
DX).
表面粗さは、5X5mmの試験片を用い、三次元粗度計
で測定した平均粗さ(SRa)で示した。The surface roughness was expressed as an average roughness (SRa) measured with a three-dimensional roughness meter using a 5×5 mm test piece.
材料特性は、引張試験(〒値)、平底円筒絞り試験(L
、D、R,) 、ビッカース硬度、耐パウダリング性、
耐クレーター性について試験・評価した。 試験・評価
条件は以下の通りである。Material properties were determined by tensile test (〒 value), flat bottom cylindrical drawing test (L
, D, R,), Vickers hardness, powdering resistance,
Crater resistance was tested and evaluated. The test/evaluation conditions are as follows.
引張試験は、JISS号試験片を引張速度10mm/m
in で引っ張り、降伏点(ys)、引張強度(TS
)および伸び(Eu)を求めた。 また、与ひずの15
%での板厚、板幅を測定し、〒値を求めた。In the tensile test, the JISS No. test piece was pulled at a speed of 10 mm/m.
In tensile strength, yield point (ys), tensile strength (TS
) and elongation (Eu) were determined. Also, 15 of the applied strain
The plate thickness and plate width in % were measured and the 〒 value was determined.
平底円筒絞り試験は、ポンチ径33mm、絞り速度0.
5mm/see、、 しわ押え圧300 kgf とし
、憫滑油としてタフ二オイルコート Z5(出光)を用
い、通常の方法て行った。 ビッカース硬度は、マイク
ロビッカース硬度側を用い、η相を除<GA層(比較例
Q−V)については各相を断面から、η相(比較例S)
および上層めっき(本発明例)については、20〜30
g / m 2の目イ寸量になるように冷延鋼板にめ
っきした別サンプルを用い、表面から、05〜5gの荷
重で圧子を押し込み、顕微鏡で圧痕を測定して求めた。The flat bottom cylindrical drawing test was performed using a punch diameter of 33 mm and a drawing speed of 0.
5 mm/see, wrinkle press pressure was set to 300 kgf, Toughuni Oil Coat Z5 (Idemitsu) was used as a lubricating oil, and the usual method was used. For Vickers hardness, use the micro Vickers hardness side, excluding the η phase.
and for upper layer plating (example of the present invention), 20 to 30
Using another sample plated on a cold-rolled steel plate to a rough size of g/m2, an indenter was pressed into the surface with a load of 0.5 to 5 g, and the indentation was measured using a microscope.
耐パウダリング性は、鋼板(40mm幅)を】Rて90
°内曲げ戻しし、その際に剥離するめっきを、あらかし
めす占りイ寸けておいたセロテープて採取し、Znの螢
光X線(照射X線発生電流 1.6mA)をカラン1−
(cps)して評価した。Powdering resistance is determined by using a steel plate (40mm width) with R = 90.
The plating that peels off during bending back is collected with cellophane tape that has been roughly measured, and the fluorescent X-rays of Zn (irradiated X-ray generation current 1.6 mA) are
(cps) and evaluated.
耐クレーター性は、鋼板に浸漬法でリン酸塩系の化成処
理を行った後に、カチオン電着塗装を行い、クレータ−
の発生ずる電圧を測定し、その電圧(V)で評価した。Crater resistance is determined by applying cationic electrodeposition coating to the steel plate after applying phosphate-based chemical conversion treatment using a dipping method.
The voltage generated was measured, and evaluation was made based on the voltage (V).
電着条件は、極比(対極/サンプル)2、極間40
mm、電着膜厚20±5μmとした。Electrodeposition conditions were: electrode ratio (counter electrode/sample) 2, electrode spacing 40.
mm, and the electrodeposited film thickness was 20±5 μm.
耐パウダリング性および耐クレーター性の評価基準は、
表1に示した。The evaluation criteria for powdering resistance and cratering resistance are as follows:
It is shown in Table 1.
表 1
第1図から明らかなように、本発明のGA錆鋼板白ぬき
)はり、D、Rか高く、プレス成形性、深絞り性か良い
。 また、L、D、Rは〒値とよい正の相関を示す。Table 1 As is clear from FIG. 1, the GA rust steel sheet of the present invention has high strength, D, and R, and good press formability and deep drawability. Furthermore, L, D, and R show a good positive correlation with the 〒 value.
これに刻し、従来のGA錆鋼板黒丸)tfL、D、
Rか低くプレス成形+4か悪い。 また、L、D、R
は材質(〒値)に依存しない。Engraved on this, conventional GA rust steel plate black circle) tfL, D,
R is low and press molding +4 is bad. Also, L, D, R
does not depend on the material (〒 value).
さらに、表4から明らかなように、本発明のGA錆鋼板
いずれもビッカース硬度か高く、耐バウタリング性およ
び耐クレーター性か良好であるか、従来のGA錆鋼板、
耐パウタリング性は良好であるものの、ビッカース硬度
か低く、耐クレーター性に問題かある。Furthermore, as is clear from Table 4, the GA rust steel sheets of the present invention all have high Vickers hardness, good bowering resistance and cratering resistance, and the conventional GA rust steel sheets,
Although the powdering resistance is good, the Vickers hardness is low and there are problems with crater resistance.
(発明の効果)
本発明は、GA wI板のプレス加工に際して、プレス
成形性かよく、母材鋼板の材料特性とおりの十分な深絞
り性を発揮し、がつ、十分な耐パウタリング性を有する
GA錆鋼板提供てきるという効果かある。(Effects of the Invention) The present invention has good press formability, sufficient deep drawability according to the material properties of the base steel plate, and has sufficient powdering resistance when press working a GA wI plate. It has the effect of being able to provide GA rusted steel plates.
第1図は、未発明のGA錆鋼板よび従来のGA錆鋼板、
引張試験におりるT値と、平底円筒絞り試験における限
界絞り比
(L、D、R,) との関係を示したグラフである。Figure 1 shows an uninvented GA rust steel plate, a conventional GA rust steel plate,
It is a graph showing the relationship between the T value in the tensile test and the critical drawing ratio (L, D, R,) in the flat bottom cylindrical drawing test.
Claims (4)
より成る合金化溶融亜鉛めっき層を有し、該合金化溶融
亜鉛めっき層上に、ビッカース硬度400以上のFeま
たはFe系合金めっき層を有することを特徴とするプレ
ス成形性に優れる合金化溶融亜鉛めっき鋼板。(1) On at least one surface of the steel sheet, there is an alloyed hot-dip galvanized layer made of an Fe-Zn alloy, and on the alloyed hot-dip galvanized layer, there is a Fe or Fe-based alloy plated layer with a Vickers hardness of 400 or more. An alloyed hot-dip galvanized steel sheet having excellent press formability.
m^2以上10g/m^2以下である請求項1に記載の
プレス成形性に優れる合金化溶融亜鉛めっき鋼板。(2) The amount of deposited Fe or Fe-based alloy plating layer is 2g/
The alloyed hot-dip galvanized steel sheet with excellent press formability according to claim 1, which has a tensile strength of not less than m^2 and not more than 10 g/m^2.
相、またはδx相、ζ相およびη相の混相より成る請求
項1または2に記載のプレス成形性に優れる合金化溶融
亜鉛めっき鋼板。(3) The alloyed hot-dip galvanized steel sheet with excellent press formability according to claim 1 or 2, wherein the alloyed hot-dip galvanized layer consists of a mixed phase of δx phase and ζ phase, or a mixed phase of δx phase, ζ phase, and η phase. .
Cr、Mn、Co、Ni、Zn、Mo、Sn、W、Re
、Pbのうちより選ばれた1種または2種以上の元素を
含有して成る請求項1〜3のいずれかに記載のプレス成
形性に優れる合金化溶融亜鉛めっき鋼板。(4) Fe-based alloy plating layer includes B, P, S, Ti, V,
Cr, Mn, Co, Ni, Zn, Mo, Sn, W, Re
4. The alloyed hot-dip galvanized steel sheet having excellent press formability according to any one of claims 1 to 3, which contains one or more elements selected from Pb, Pb, and Pb.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63152685A JPH01319661A (en) | 1988-06-21 | 1988-06-21 | Alloying hot dip galvanized steel sheet excellent in press formability |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63152685A JPH01319661A (en) | 1988-06-21 | 1988-06-21 | Alloying hot dip galvanized steel sheet excellent in press formability |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH01319661A true JPH01319661A (en) | 1989-12-25 |
Family
ID=15545884
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63152685A Pending JPH01319661A (en) | 1988-06-21 | 1988-06-21 | Alloying hot dip galvanized steel sheet excellent in press formability |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH01319661A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5629099A (en) * | 1993-06-30 | 1997-05-13 | Nkk Corporation | Alloying-treated iron-zinc alloy dip-plated steel sheet excellent in press-formability and method for manufacturing same |
| US6699592B2 (en) | 2000-04-24 | 2004-03-02 | Nkk Corporation | Galvannealed steel sheet and method for manufacturing the same |
| WO2007129678A1 (en) | 2006-05-02 | 2007-11-15 | Jfe Steel Corporation | Process for producing alloyed hot-dip zinc-plated steel sheet and alloyed hot-dip zinc-plated steel sheet |
| WO2009031699A1 (en) | 2007-09-04 | 2009-03-12 | Jfe Steel Corporation | Galvanized steel sheet |
| JP2009235431A (en) * | 2008-03-26 | 2009-10-15 | Jfe Steel Corp | Galvanized steel sheet and manufacturing method therefor |
| US8025980B2 (en) | 2003-08-29 | 2011-09-27 | Jfe Steel Corporation | Hot dip galvanized steel sheet and method for manufacturing same |
| WO2014002428A1 (en) | 2012-06-25 | 2014-01-03 | Jfeスチール株式会社 | Alloyed zinc-plated steel sheet having excellent anti-powdering properties |
-
1988
- 1988-06-21 JP JP63152685A patent/JPH01319661A/en active Pending
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5629099A (en) * | 1993-06-30 | 1997-05-13 | Nkk Corporation | Alloying-treated iron-zinc alloy dip-plated steel sheet excellent in press-formability and method for manufacturing same |
| US6699592B2 (en) | 2000-04-24 | 2004-03-02 | Nkk Corporation | Galvannealed steel sheet and method for manufacturing the same |
| US8815349B2 (en) | 2003-08-29 | 2014-08-26 | Jfe Steel Corporation | Hot dip galvanized steel sheet and method for manufacturing same |
| US8025980B2 (en) | 2003-08-29 | 2011-09-27 | Jfe Steel Corporation | Hot dip galvanized steel sheet and method for manufacturing same |
| WO2007129678A1 (en) | 2006-05-02 | 2007-11-15 | Jfe Steel Corporation | Process for producing alloyed hot-dip zinc-plated steel sheet and alloyed hot-dip zinc-plated steel sheet |
| US8268095B2 (en) | 2006-05-02 | 2012-09-18 | Jfe Steel Corporation | Method of manufacturing hot dip galvannealed steel sheet and hot dip galvannealed steel sheet |
| US8221900B2 (en) | 2007-09-04 | 2012-07-17 | Jfe Steel Corporation | Zinc-based metal plated steel sheet |
| US8623514B2 (en) | 2007-09-04 | 2014-01-07 | Jfe Steel Corporation | Zinc-based metal plated steel sheet |
| WO2009031699A1 (en) | 2007-09-04 | 2009-03-12 | Jfe Steel Corporation | Galvanized steel sheet |
| USRE45821E1 (en) | 2007-09-04 | 2015-12-22 | Jfe Steel Corporation | Zinc-based metal plated steel sheet |
| JP2009235431A (en) * | 2008-03-26 | 2009-10-15 | Jfe Steel Corp | Galvanized steel sheet and manufacturing method therefor |
| WO2014002428A1 (en) | 2012-06-25 | 2014-01-03 | Jfeスチール株式会社 | Alloyed zinc-plated steel sheet having excellent anti-powdering properties |
| US9828663B2 (en) | 2012-06-25 | 2017-11-28 | Jfe Steel Corporation | Galvannealed steel sheet with excellent anti-powdering property |
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