JPS5864367A - Production of zinc hot dipped steel plate - Google Patents
Production of zinc hot dipped steel plateInfo
- Publication number
- JPS5864367A JPS5864367A JP56163071A JP16307181A JPS5864367A JP S5864367 A JPS5864367 A JP S5864367A JP 56163071 A JP56163071 A JP 56163071A JP 16307181 A JP16307181 A JP 16307181A JP S5864367 A JPS5864367 A JP S5864367A
- Authority
- JP
- Japan
- Prior art keywords
- steel plate
- hot
- steel
- temperature
- rimmed
- 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
- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 32
- 239000010959 steel Substances 0.000 title claims abstract description 32
- 239000011701 zinc Substances 0.000 title claims abstract description 13
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 title claims abstract description 12
- 229910052725 zinc Inorganic materials 0.000 title claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910001327 Rimmed steel Inorganic materials 0.000 claims abstract description 10
- 238000007747 plating Methods 0.000 claims description 12
- 229910001335 Galvanized steel Inorganic materials 0.000 claims description 9
- 239000008397 galvanized steel Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 abstract description 22
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 11
- 239000001257 hydrogen Substances 0.000 abstract description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract description 10
- 238000010438 heat treatment Methods 0.000 abstract description 10
- 238000005098 hot rolling Methods 0.000 abstract description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 6
- 229910052799 carbon Inorganic materials 0.000 abstract description 6
- 229910052757 nitrogen Inorganic materials 0.000 abstract description 5
- 238000005554 pickling Methods 0.000 abstract description 3
- 230000003247 decreasing effect Effects 0.000 abstract 4
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 208000002352 blister Diseases 0.000 abstract 1
- 238000007598 dipping method Methods 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 238000004804 winding Methods 0.000 description 16
- 238000001556 precipitation Methods 0.000 description 14
- 239000006104 solid solution Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229910000655 Killed steel Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000011946 reduction process Methods 0.000 description 2
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005246 galvanizing Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000001000 micrograph Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C23C2/34—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the shape of the material to be treated
- C23C2/36—Elongated material
- C23C2/40—Plates; Strips
- C23C2/405—Plates of specific length
-
- 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
- C23C2/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
- C23C2/022—Pretreatment of the material to be coated, e.g. for coating on selected surface areas by heating
- C23C2/0222—Pretreatment of the material to be coated, e.g. for coating on selected surface areas by heating in a reactive atmosphere, e.g. oxidising or reducing atmosphere
-
- 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
- C23C2/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
- C23C2/024—Pretreatment of the material to be coated, e.g. for coating on selected surface areas by cleaning or etching
Abstract
Description
【発明の詳細な説明】
、本発明は、めっき後、めっき層に発生するブリスター
の防止をはかった熱延溶融亜鉛めっき鋼板の製造方法に
関するものであ、る。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a hot-rolled hot-dip galvanized steel sheet that prevents blisters from occurring in the plating layer after plating.
従来より、厚手溶融亜鉛めっき鋼板の原板としては熱延
鋼板が使用されている。この熱延鋼板を原板とする溶融
亜鉛めっき鋼板は、必要に応じて酸洗することによりス
ケールを除去し、ついでシーラス法、ゼンジマー法等に
より水素ガスを含有する雰囲気ガス(多くの場合、H2
10〜75%、Nwg6〜25%)で加熱還元し、その
後溶融亜鉛に浸漬することにより行なわれているのが一
般的である。Conventionally, hot-rolled steel sheets have been used as base sheets for thick hot-dip galvanized steel sheets. Hot-dip galvanized steel sheets using this hot-rolled steel sheet as the base sheet are subjected to pickling as necessary to remove scale, and then processed using an atmospheric gas containing hydrogen gas (in most cases, H2
It is generally carried out by heating reduction with 10 to 75% Nwg and 6 to 25% Nwg, and then immersing it in molten zinc.
しかし、原板として熱延鋼板を用いた場合、加熱還元工
程において水素を吸蔵し、それがめつき後に放出される
ために、η−亜鉛めっき層を押上げ、めっき鋼板表面に
多数のブリスター(ふくれ)を発生させるという問題が
ある。この問題はシーラス法、ゼンジマー法、USスチ
ール法等、一般に鋼板表面を水素を含む雰囲気ガス中で
加熱還元するめつき方法においては、程度の差はあれ発
生しており、このため、従来より種々の解決策が提案さ
れている。However, when a hot-rolled steel sheet is used as the original sheet, hydrogen is absorbed during the heating reduction process and released after plating, which pushes up the η-galvanized layer and causes numerous blisters on the surface of the plated steel sheet. There is a problem in that it causes This problem occurs to varying degrees in plating methods such as the Cirrus method, Sendzimer method, and US Steel method, in which the surface of a steel sheet is heated and reduced in an atmospheric gas containing hydrogen. A solution is proposed.
たとえば、その解決策として従来より提案されている方
法に、亜鉛浴組成の改善がある。この方法には、亜鉛浴
中にブリスター発生防止剤として、S、 Se、 P、
As、 Te、 Sb、 Bi、の5ちの1種または
2種以上を添加する方法(特開昭49−14325号)
、鋼板を750〜Acs点の範囲の温度で還元し、それ
をAIo、22〜0.35重量係含有する亜°鉛浴でめ
っきする方法(@開昭54−26928号)等が。知ら
れているが、前者の方法はブリスター発生防止剤を均一
に分散させるため、添加の際に亜鉛合金の状態で添加し
なければならず、このためその合金の製造に多くの費用
がかかるという欠点がある。また、後者の方法にしても
亜鉛浴中のAI濃度が高くなるため、作業性と品質が損
なわれたり、製造コストが上昇するという問題がある。For example, one method that has been proposed in the past as a solution to this problem is to improve the composition of the zinc bath. In this method, S, Se, P,
A method of adding one or more of As, Te, Sb, and Bi (Japanese Unexamined Patent Publication No. 14325/1983)
, a method in which a steel plate is reduced at a temperature in the range of 750 to Acs point, and then plated in a zinc bath containing 22 to 0.35% AIo (by weight) (@Kaisei No. 54-26928). However, in the former method, in order to uniformly disperse the blister-preventing agent, it must be added in the form of a zinc alloy, which increases the cost of manufacturing the alloy. There are drawbacks. Furthermore, even if the latter method is used, the concentration of AI in the zinc bath increases, resulting in problems such as deterioration of workability and quality, and increase in manufacturing costs.
また、他の解決策として加熱還元温度を低下させる方法
がある。この方法は、従来、加熱還元を800〜850
t:’で実施していたのを600〜720t:”で実施
しようとするものである。(特開昭、52−95543
号)、シかし、このように加熱還元温度を低下させた場
合には、めっき速度をいる。Further, as another solution, there is a method of lowering the heating reduction temperature. This method conventionally involves thermal reduction of 800 to 850
This is an attempt to implement the method that was used for 600 to 720 t:'' instead of 600 to 720 t:''.
However, if the heating reduction temperature is lowered in this way, the plating rate will be lowered.
その他の解決策としては、加熱還元工程において吸蔵し
た水素を後工程で脱水素処理し、その後で溶融亜鉛めっ
きする方法がある。この方法は、1−(28−20%、
N292−80%の雰囲気中に、450〜550Cの温
度の鋼板を導いて脱水素しようとするもの(特開昭54
°−130443号)であるが、実際のめつきラインに
おいてこのような脱水゛素処理工程を設けるには多額の
費用を要し、設備的に、また製造技術の面でも極めて困
難である。さらに、従来のめつきラインには、このよう
な工程を設ける場所的余裕がないのが実状である。Another solution is to dehydrogenate the hydrogen occluded in the thermal reduction process in a subsequent process, and then hot-dip galvanize. This method uses 1-(28-20%,
A method in which a steel plate at a temperature of 450 to 550C is introduced into an atmosphere of 80% N292 to dehydrogenate it (Japanese Patent Laid-Open No. 1983-1999)
However, providing such a dehydration process in an actual plating line requires a large amount of cost and is extremely difficult in terms of equipment and manufacturing technology. Furthermore, the reality is that conventional plating lines do not have space for such a process.
X発明は、前述のような亜鉛浴組成や加熱還元温度−の
変更、または脱水素処理工程の付加等によらず、熱延鋼
板そのものの改善によりブリスター発生を防止した溶融
亜鉛めっき鋼板の製造方法を提供しようとするものであ
る。Invention X is a method for producing a hot-dip galvanized steel sheet that prevents blistering by improving the hot-rolled steel sheet itself, without changing the zinc bath composition or heating reduction temperature or adding a dehydrogenation process as described above. This is what we are trying to provide.
水素ガスによる加熱還元方式の溶融亜鉛めっきにおいて
、熱延亜鉛めっき鋼ゝ板にブリスターを発生させないよ
うKするためには、加熱還元の際に鋼板が吸蔵する水素
量を少なくするのが理想的である。このためには加熱還
元時の鋼板温度、雰囲気圧力、さらには水素濃度を出来
るだけ低くすれば良い。しかし、これらの要因を低く保
持することは、生産性を低下させ、極端な場合には不め
っき欠陥につながるので最終的には製品コストを上昇さ
せることになる。In hot-dip galvanizing using a heating reduction method using hydrogen gas, in order to prevent blisters from forming on hot-rolled galvanized steel sheets, it is ideal to reduce the amount of hydrogen absorbed by the steel sheet during heating reduction. be. For this purpose, the steel plate temperature, atmospheric pressure, and hydrogen concentration during thermal reduction should be made as low as possible. However, keeping these factors low reduces productivity and, in extreme cases, leads to unplated defects, ultimately increasing product costs.
そこで本発明者らは、生産性の低下をもたらせないで、
ブリスターの発生を減少させる方法として、鋼中の炭素
、窒素等、熱間圧延時の巻取後に析出する元素が微細に
析出するのを抑制し、その結果として鋼中の炭素、窒素
等の固溶量を増大させて水素の吸蔵量を減少させる方法
に着目して研究した。そして、その具体的手段として、
リムド鋼の場合、熱間圧延における巻取を高温巻取にす
れば良いことを知見した。Therefore, the inventors of the present invention solved the problem without causing a decrease in productivity.
One way to reduce the occurrence of blisters is to suppress the fine precipitation of elements such as carbon and nitrogen in steel that precipitate after coiling during hot rolling. The research focused on a method of increasing the amount of dissolved hydrogen and reducing the amount of hydrogen absorbed. And as a concrete means,
In the case of rimmed steel, it has been found that it is sufficient to use high-temperature coiling for hot rolling.
たとえば炭素の場合、熱間圧延における仕上温度が同一
であれば、巻取後冷却の際に発生する炭化物の析出は粗
く、かつ大きくなる。第1区内、β)はリムド鋼のこの
両巻取における炭化物析出状態を示すもので、(8)は
通常巻取(5ssc)、(B)は高温巻取(730C)
の場合で、高温巻取の場合、炭化物析出は粗く、かつ大
きくなっている。For example, in the case of carbon, if the finishing temperature during hot rolling is the same, carbide precipitation that occurs during cooling after coiling will be coarser and larger. In the first section, β) shows the carbide precipitation state in both windings of the rimmed steel, (8) is the normal winding (5ssc), and (B) is the high temperature winding (730C).
In the case of high-temperature winding, the carbide precipitation is coarse and large.
しかして、本発明者らは、この両状態における鋼中の炭
素や窒素の固溶量と析出量との関係について種々、調査
した結果、高温巻取の方が固溶量が多ぐ、通常巻取の方
が少いことを見出した。As a result of various investigations into the relationship between the amount of solid solution and the amount of precipitation of carbon and nitrogen in steel in both these conditions, the inventors found that the amount of solid solution is greater in high temperature coiling, and that It was found that the amount of winding was smaller.
このように、巻取温度により炭素や窒素の固溶量が異な
るのは、冷却の際に発生する析出核密度に起因するもの
y考えられる。すなわち、炭素や窒素などの析出元素は
冷却の際に過飽和の状態で徐々に冷されるが、熱延コイ
ルのよう・・に析出時間がかなりある場合には、その析
出速度は、析出核が密に外布していて、その核と核との
距離が短い場合に速くなる。このため、析出核密度の高
い通常巻取の場合容易に析出し、析出物周囲の固溶量が
減少して、鋼全体としての平均固溶量は低くなる。これ
に対して、高温巻取の場合には析出核が粗いため、析出
核より離れた部分の元素は容易に析出できず、固溶され
たま〜になっているものと考えられる。The reason why the amount of solid solution of carbon and nitrogen differs depending on the coiling temperature is considered to be due to the density of precipitation nuclei generated during cooling. In other words, precipitated elements such as carbon and nitrogen are gradually cooled in a supersaturated state during cooling, but in cases where there is a considerable amount of precipitation time, such as in hot-rolled coils, the precipitation rate is determined by the amount of precipitation nuclei. It becomes faster when the cores are densely distributed and the distance between the cores is short. Therefore, in the case of normal winding where the density of precipitation nuclei is high, precipitation occurs easily, the amount of solid solution around the precipitates decreases, and the average amount of solid solution for the steel as a whole becomes low. On the other hand, in the case of high-temperature winding, since the precipitation nuclei are rough, it is thought that the elements in the portions away from the precipitation nuclei cannot be easily precipitated and remain in solid solution.
そして、本発明者らの調査によれば、リムド鋼の場合に
は、上記輝温巻取の温度を650t:’以上にすればブ
リスター防止に効果があるが、キルド鋼に関しては、は
とんど効果がないことが判明している。従って、本発明
はリムド熱延鋼板を原板とする溶融亜鉛めっき鋼板の製
造方法を対象とするものである。According to the research conducted by the present inventors, in the case of rimmed steel, setting the bright temperature winding temperature to 650 t:' or higher is effective in preventing blisters, but in the case of killed steel, it is extremely effective. It has been proven to be ineffective. Therefore, the present invention is directed to a method of manufacturing a hot-dip galvanized steel sheet using a rimmed hot-rolled steel sheet as an original sheet.
以下、実施例により本発明を説明する。The present invention will be explained below with reference to Examples.
第1表に示すリムド鋼を仕上温度を900 C一定のも
とに熱間圧延して、それを585C(通常巻取)、65
0Cおよび730C(高温巻取)°で巻取った熱延鋼帯
(板厚2.3■、巾920■)の中央部より150 X
250III+の試料を採取し、これを硫酸、塩酸の
混酸で酸洗してスケールを除去し、さらに8275%、
N225%、温度650Cの雰囲気(露6点−400)
中に15仲間保持して鋼板の表面を還元し、活性化した
。The rimmed steel shown in Table 1 was hot rolled at a constant finishing temperature of 900C, then rolled at 585C (normal winding) and 65C.
150X from the center of a hot rolled steel strip (thickness 2.3cm, width 920cm) wound at 0C and 730C (high temperature winding)°
A sample of 250III+ was taken, and it was pickled with a mixed acid of sulfuric acid and hydrochloric acid to remove scale, and further reduced to 8275%.
N225%, temperature 650C atmosphere (dew 6 points - 400)
The surface of the steel plate was reduced and activated by holding 15 members inside.
第 1 表
になったときに、Aso、xsmの亜鉛浴(450c)
に2秒間浸漬して亜鉛めっきを行ない、鋼板中の吸蔵水
素量およびめっき表面のブリスター発生数を調査した。When Table 1 is reached, Aso, xsm zinc bath (450c)
Zinc plating was performed by immersing the steel sheet in water for 2 seconds, and the amount of absorbed hydrogen in the steel sheet and the number of blisters generated on the plating surface were investigated.
第2表はこの結果を示すもので、ブリスター発生数の少
ないものは水素吸蔵量が少なく、かつ巻取温度を650
C以上にするとブリスター発生数が少ないことがわかる
。Table 2 shows the results, and shows that those with a small number of blisters have a small amount of hydrogen storage, and the winding temperature is 650.
It can be seen that when the temperature is C or higher, the number of blisters generated is small.
第 2 表
(注1)ブリスター数はめっき鋼板を1週間・室温で放
置した後、η−Znめっき層の
(0001)結晶面について、1cd当りの数を30倍
や拡大鏡により観察して数えた。Table 2 (Note 1) The number of blisters is determined by leaving the plated steel plate at room temperature for one week, and then observing the number per 1 cd of the (0001) crystal plane of the η-Zn plating layer using a 30x magnifying glass or counting. Ta.
(注2)水素量(量は、真空加熱式ガス質量分析装置に
試料を一定量装入し、500 c。(Note 2) Amount of hydrogen (amount is 500 c when a certain amount of sample is charged into a vacuum heating gas mass spectrometer.
(2〜5)X10Torr下において検出されるH2ピ
ークの積分値によった。(2-5) Based on the integral value of the H2 peak detected under X10 Torr.
また、第2図は巻取温度585c、650rおよび73
0Cのもののブリスター発生状況を板巾方向について調
査したもので、巻取温度を高くすると、板巾全体にわた
りブリスター発生数は少なくなる。さらに、第3図は第
3表に示す化学成分のアルミキルド鋼を910cの一定
仕上温度で熱間圧延後、585cおよび730rで巻取
った熱延鋼帯を前記同様にしてめっきした場合のブリス
ター発生数を示したもので、アルミキルド鋼ヲ原板とす
る場合はリムド鋼(so 1.AI ; t r、)の
場合と異なり12巻取温度を高くしても、?°リスター
発生の低減効果はあまり認められない−
第 3 表
以上の如(、本発明によれば、リムド熱延鋼板を原板と
する場合に限り、めっき後に発生するブリスター数を大
巾に減少させることが出来る。しかも、本発明の場合、
熱間圧延における巻取温度を変更することにより、ブリ
スター発生数を減少させるのであるから、特別な設備を
必要とせず、生産性も従来と同一の水準に維持する・こ
とが出来る。In addition, Fig. 2 shows winding temperatures of 585c, 650r and 73
This study investigated the occurrence of blisters in the width direction of the board at 0C, and as the winding temperature is increased, the number of blisters generated across the board width decreases. Furthermore, Figure 3 shows the occurrence of blisters when a hot-rolled steel strip having the chemical composition shown in Table 3 was hot-rolled at a constant finishing temperature of 910c and then coiled at 585c and 730r and plated in the same manner as above. The numbers show that when aluminum killed steel is used as the original plate, unlike the case of rimmed steel (so 1.AI; tr,), even if the coiling temperature is raised, ? ° The effect of reducing the occurrence of listers is not so recognized - As shown in Table 3 (according to the present invention, the number of blisters that occur after plating can be greatly reduced only when a rimmed hot rolled steel sheet is used as the base plate) Furthermore, in the case of the present invention,
By changing the winding temperature during hot rolling, the number of blisters generated is reduced, so no special equipment is required and productivity can be maintained at the same level as before.
第1図は熱間圧延後の巻取温度の相異によるリムド鋼板
の炭化物析出状態を示した顕微鏡写真で。
(A)は巻取温度585iCS(B)は730Cの場合
を示している。
ミキルド鋼の溶融亜鉛めっき鋼板の5olAIとプリス
、ター発生数との関係に及ぼす熱延巻取温度の影響を示
すものである。
第2 図
オフ乏巾 (920綽O−ン
第3図
5etf1.Nl (X/−%)Figure 1 is a micrograph showing the state of carbide precipitation in a rimmed steel sheet due to differences in coiling temperature after hot rolling. (A) shows the case where the winding temperature is 585iCS (B) is 730C. This figure shows the influence of the hot rolling winding temperature on the relationship between 5olAI and the number of splinters and tars generated in a hot-dip galvanized steel sheet made of MIKILD steel. Fig. 2 Off width (920 tangle O-on Fig. 3 5etf1.Nl (X/-%)
Claims (1)
還元し、その後溶融亜鉛に浸漬してめっきする溶融亜鉛
めっき鋼板の製造方法において、前記熱延鋼板として、
熱間圧延後650C以上の温度で巻取ったリムド鋼板を
用いる。ことを特徴とする溶融亜鉛めっき鋼板の製造方
法。In a method for producing a hot-dip galvanized steel sheet in which a hot-rolled steel sheet is pickled, then heated and reduced in an atmosphere containing hydrogen gas, and then immersed in hot-dip zinc for plating, the hot-rolled steel sheet includes:
A rimmed steel plate that is hot-rolled and then rolled up at a temperature of 650C or higher is used. A method for producing a hot-dip galvanized steel sheet.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56163071A JPS5864367A (en) | 1981-10-13 | 1981-10-13 | Production of zinc hot dipped steel plate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56163071A JPS5864367A (en) | 1981-10-13 | 1981-10-13 | Production of zinc hot dipped steel plate |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5864367A true JPS5864367A (en) | 1983-04-16 |
Family
ID=15766622
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56163071A Pending JPS5864367A (en) | 1981-10-13 | 1981-10-13 | Production of zinc hot dipped steel plate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5864367A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03232952A (en) * | 1990-02-07 | 1991-10-16 | Kawasaki Steel Corp | Manufacture of hot-dip galvanized steel sheet having good adhesion of galvanizing layer |
-
1981
- 1981-10-13 JP JP56163071A patent/JPS5864367A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03232952A (en) * | 1990-02-07 | 1991-10-16 | Kawasaki Steel Corp | Manufacture of hot-dip galvanized steel sheet having good adhesion of galvanizing layer |
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