JPS6115946B2 - - Google Patents
Info
- Publication number
- JPS6115946B2 JPS6115946B2 JP55119815A JP11981580A JPS6115946B2 JP S6115946 B2 JPS6115946 B2 JP S6115946B2 JP 55119815 A JP55119815 A JP 55119815A JP 11981580 A JP11981580 A JP 11981580A JP S6115946 B2 JPS6115946 B2 JP S6115946B2
- Authority
- JP
- Japan
- Prior art keywords
- plating
- steel strip
- molten metal
- film
- solution
- 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.)
- Expired
Links
- 238000007747 plating Methods 0.000 claims description 74
- 229910000831 Steel Inorganic materials 0.000 claims description 66
- 239000010959 steel Substances 0.000 claims description 66
- 238000000034 method Methods 0.000 claims description 31
- 239000002184 metal Substances 0.000 claims description 23
- 229910052751 metal Inorganic materials 0.000 claims description 23
- 238000000576 coating method Methods 0.000 claims description 18
- 239000000243 solution Substances 0.000 claims description 18
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 17
- 239000011248 coating agent Substances 0.000 claims description 17
- 239000007787 solid Substances 0.000 claims description 17
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 238000002485 combustion reaction Methods 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 6
- 150000002430 hydrocarbons Chemical class 0.000 claims description 6
- 235000019353 potassium silicate Nutrition 0.000 claims description 6
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 6
- 239000007864 aqueous solution Substances 0.000 claims description 5
- 229920003002 synthetic resin Polymers 0.000 claims description 4
- 239000000057 synthetic resin Substances 0.000 claims description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 3
- 229910021538 borax Inorganic materials 0.000 claims description 3
- 229920002050 silicone resin Polymers 0.000 claims description 3
- 239000004328 sodium tetraborate Substances 0.000 claims description 3
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 3
- 230000002265 prevention Effects 0.000 claims description 2
- 229920002379 silicone rubber Polymers 0.000 claims description 2
- 239000004945 silicone rubber Substances 0.000 claims description 2
- 229920005992 thermoplastic resin Polymers 0.000 claims 1
- 239000011247 coating layer Substances 0.000 description 16
- 230000003647 oxidation Effects 0.000 description 14
- 238000007254 oxidation reaction Methods 0.000 description 14
- 239000004071 soot Substances 0.000 description 14
- 238000005275 alloying Methods 0.000 description 9
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 7
- 238000001035 drying Methods 0.000 description 7
- 230000004907 flux Effects 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- 229910052725 zinc Inorganic materials 0.000 description 7
- 239000011701 zinc Substances 0.000 description 7
- 238000005260 corrosion Methods 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 5
- 230000000873 masking effect Effects 0.000 description 5
- 229910001335 Galvanized steel Inorganic materials 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000008397 galvanized steel Substances 0.000 description 4
- 230000001680 brushing effect Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000005246 galvanizing Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000002966 varnish Substances 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 238000005554 pickling Methods 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 239000007790 solid phase Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- 239000004265 EU approved glazing agent Substances 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- -1 etc. Chemical compound 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 230000008674 spewing Effects 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 238000004017 vitrification Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 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
- C23C2/003—Apparatus
- C23C2/0034—Details related to elements immersed in bath
- C23C2/00342—Moving elements, e.g. pumps or mixers
- C23C2/00344—Means for moving substrates, e.g. immersed rollers or immersed bearings
-
- 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
- C23C2/003—Apparatus
- C23C2/0038—Apparatus characterised by the pre-treatment chambers located immediately upstream of the bath or occurring locally before the dipping process
-
- 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
- C23C2/003—Apparatus
- C23C2/0038—Apparatus characterised by the pre-treatment chambers located immediately upstream of the bath or occurring locally before the dipping process
- C23C2/004—Snouts
-
- 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
- C23C2/022—Pretreatment of the material to be coated, e.g. for coating on selected surface areas by heating
- C23C2/0224—Two or more thermal pretreatments
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Coating With Molten Metal (AREA)
- Chemical Vapour Deposition (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Description
〔産業上の利用分野〕
本発明は、予め、鋼帯のめつき不要面にめつき
防止膜を形成させた後、鋼帯を溶融金属めつき浴
に浸漬するめつき方法に係り、特に鋼帯の一部分
にのみ例えば片面にのみめつきを施すような鋼帯
の部分溶融金属めつき方法に関する。
〔従来の技術〕
鋼板に耐食性を付与するため、種々の耐食性皮
膜を鋼板表面に形成することが多い。この場合、
鋼板の両面に耐食性皮膜を形成するのが一般的で
ある。しかし自動車用鋼板の如くめつき後に塗装
するものについては、めつき面に塗装を施すと鮮
映性に劣り、商品価値を著しく減じる。また、例
えば、亜鉛めつき鋼板の溶接性は、亜鉛の融点と
沸点との差が小さくかつ熱伝導性が大きいこと、
また、電極を汚染しやすいことなどの理由から好
ましくない。このように鋼板表面に耐食性を付与
することと、溶接性及び塗装後鮮映性とは、相反
する性質をもつている。このため自動車用鋼板等
では、鋼板の片面のみをめつきして、耐食性を付
与し、他面に対しては塗装性と溶接性をもたせた
いわゆる片面めつき鋼板が使用されつつある。
〔発明が解決しようとする問題点〕
溶融金属めつき例えば溶融亜鉛めつきで片面亜
鉛めつき鋼板を製造する方法には、鋼板のめつき
不要面にめつき防止膜を形成する方法、超音波あ
るいはロール等により機械的に溶融亜鉛を鋼板の
片面のみに接触させる方法、あるいは両面めつき
後に片面の亜鉛を研削除去する方法などがある。
このうち機械的な方法は技術的に困難なため実用
的でなく、さらに片面の亜鉛を研削除去する方法
はコストが高い欠点がある。
これらのことから、めつき不要面にめつき防止
膜を形成する方法が種々提案され、めつき防止剤
としては水ガラス、シリコーン樹脂、酸化膜、ア
ルミナ、カーボン等が知られている。これらめつ
き防止剤の中で、炭化水素燃料の不完全燃焼によ
り発生させたカーボン、いわゆるすすは、溶融亜
鉛と反応せず、また濡れ性が非常に小さいため、
めつき防止性能が非常に高い。またすすは自己潤
滑性があり、すす面の摩擦係数が小さいので、鋼
帯がめつき浴から高速で引き上げられる時に、溶
融亜鉛を引き上げる量が極めて少ない。しかしす
すは多孔質であるから、鋼帯面にすすのめつき防
止膜を形成しても、この膜を通して大気中の酸素
が鋼帯面に侵入する。このため、溶融めつき後、
非めつき面が酸化される欠点があり、特にめつき
後に合金化処理する場合、500℃程度に加熱され
るので、酸化の進行が一層激しくなる。
一方、すす以外のめつき防止材は、鋼帯がめつ
き浴から高速で引き上げられる時に、同時に溶融
亜鉛を引き上げる欠点があつた。
〔発明の目的〕
本発明の目的は、前述した従来技術の欠点を解
消し、高品質の部分溶融めつき鋼帯を高速に製造
するめつき方法を提供することである。
〔問題点を解決するための手段〕
本発明は、鋼帯のめつき不要面にカーボン粉末
を含むめつき防止膜を形成し、その後鋼帯を溶融
金属めつき浴に浸漬する鋼帯の部分溶融金属めつ
き方法において、めつき不要面に、予め固形成分
を溶解した溶液の塗膜を形成し、次にこの塗膜を
乾燥させ酸素の侵入を抑制または実質的に阻止す
る層とした後、塗膜上にカーボンを含むめつき防
止膜を形成することを特徴とする。
〔作用〕
本発明による複合(2層)めつき防止膜につい
てさらに詳述する。
鋼板のめつき不要面に形成する第1の被覆層
は、固形成分を溶解した溶液を鋼板のめつき不要
面にロールコートあるいはスプレーなどの方法で
塗布する。固形成分を溶解した溶液としては、無
機質溶液あるいは合成樹脂溶液などを用いる。特
に耐熱性のすぐれたものが望ましく、例えば水ガ
ラス、アルミナ、ホウ砂水溶液、シリコーン樹脂
ワニス、あるいはシリコーンゴムワニスが最も有
用である。水ガラスは、通常、原液と称するケイ
酸アルカリ塩の濃厚水溶液を水で稀釈したものが
特に望ましく、その濃度は塗布作業に支障なく、
良好な密着性が得られ、しかも乾燥後もしくは加
熱処理によりガラス化した後は緻密な皮膜を形成
できるような濃度に適宜選択する。一般的な目安
としては0.1〜30重量%好ましくは0.5〜20重量%
である。合成樹脂ワニスあるいはホウ砂水溶液の
場合も、樹脂の種類によりその濃度を選択する
が、水ガラスの場合と同様に、作業性がよくしか
も緻密な皮膜が形成できるように適宜選択すべき
である。固形成分を溶解した溶液の塗膜に大切な
ことは、鋼帯のめつき不要面への酸素侵入を極力
阻止できるように、その皮膜が十分厚くあるいは
緻密であることである。酸素の侵入を阻止する
と、めつき終了後の加熱合金化処理の際、めつき
不要面の酸化を防止でき、極めて好都合である。
固形成分を溶解した溶液の塗膜(第1被覆層)
が実質的に乾燥した後、その上にカーボン粉末を
含むめつき防止膜を形成する。固形成分を溶解し
た溶液の塗膜の乾燥は、この塗膜乾燥用に特別の
乾燥炉を設けて行う必要はなく、酸化炉または鋼
帯に塗布されるフラツクスを乾燥させるための乾
燥炉などで行なえばよい。
カーボン粉末は定形と無定形のいずれでも使用
できる。カーボン粉末の粒径は大きすぎると、第
1被覆層との接触面積が減り、密着性が低下する
ため、可能なかぎり小さい方が好ましい。実用的
には数μm以下であれば十分である。第2皮膜層
であるカーボン粉末のめつき防止膜は、スプレー
あるいはロールコートなどで形成される。最も望
ましくは炭化水素を不完全燃焼させ、この燃焼炎
を第1被覆層に直接吹き付け、発生するすすを付
着させる方法が、密着性、粉末の粒径、第1被覆
層の固相への変換の促進などの点で有利である。
このように高密着性を有し、固相へ変換後緻密
な第1被覆層を形成し、酸素の侵入を抑制ないし
阻止すると、合金化熱処理等によつてもめつき不
要面が酸化されることがなく、高品質の片面めつ
き鋼板が得られる。
本発明方法を実施するに当つては、次のような
めつき装置が使用される。すなわち本発明方法を
実施するための鋼帯の部分溶融金属めつき装置
は、鋼帯のめつき不要面に固形成分を溶解した溶
液の塗膜を形成する装置、塗膜が実質的に乾燥し
た後、塗膜上にカーボン粉末を含むめつき防止膜
を形成する装置、溶融金属めつき浴および鋼帯の
めつき不要面上の固形成分およびカーボン粉末を
除去する装置を備えている。
〔実施例〕
次の本発明のめつき方法を図面によつてさらに
具体的に説明する。第1図〜第3図は本発明方法
を実施するためのめつき装置を示す概略図であ
る。
先ず、第1図において、鋼帯1には、そのめつ
き不要面に固形成分を溶解した溶液2例えば水ガ
ラスなどをリバースコータ3により塗工し、第1
の被覆層を形成する。次にこの第1被覆層が実質
的に湿潤状態のうち、鋼帯1は酸化炉4に入る。
酸化炉4では、鋼帯のめつき面に付着したいた油
などが燃焼させられるとともに第1被着層が乾燥
する。酸化炉4を経た鋼帯1はスロート5を通つ
た後、還元炉6に入る。還元炉6では鋼帯のめつ
き面の酸化物が還元され清浄にされる。次に鋼帯
1は、デフレクタローラ7により進行方向を変え
られた後、還元雰囲気中に配置されたプレコート
ローラ8によつてめつき面側にめつき金属9がプ
レコートされる。このプレコートは、鋼帯のめつ
き面を大気中に噴出させないための工程である。
一方非めつき面側、すなわち第1被覆層上にマス
キングバーナ10によりすすが被覆される。マス
キングバーナ10には炭化水素、例えばプロパ
ン、ブタン、アセチレン、天然ガス等と酸素ある
いは空気とを供給し、その比率を適当にすると、
燃焼炎から効率的にすすが発生する。炭化水素と
しては炭素元子含有率の高いものが特に望まし
く、アセチレンガスは効果的である。一方プロパ
ンガスあるいはブタンガスは粒子の細い炭素粉末
が得られ緻密な皮膜を形成できる利点がある。こ
の燃焼炎を第1被覆層上に吹き付けてすす皮膜を
形成し、めつき防止膜とする。
その後、鋼帯1はターンローラ11により進行
方向を変えられ、めつき浴12内の溶融金属9中
に浸漬され、シンクローラ13を経て大気中に引
き出される。この際、鋼帯1の非めつき面には酸
素の侵入を実質的に阻止する第1被覆層とすすが
被覆されているので、大気中の酸素による非めつ
き面の酸化が進行することがないか軽微であり、
また溶融金属9を同時に引き上げることが防止さ
れる。
次に鋼帯1は合金化処理炉14に入り、再び高
温例えば亜鉛めつきでは約500℃に10〜60秒保持
され、その材質が改善される。このような高温に
おいても前記2層被覆のため、めつき不要面の酸
化は防止される。合金化処理はめつき鋼帯の用途
により施す場合と必要がない場合とがある。鋼帯
1は冷却装置15により常温程度まで冷却された
後、ブラツシングロール16によりめつき不要面
の2層被覆すなわちカーボン粉末およびその他の
固形成分が研削削除され、片面めつき鋼帯が得ら
れる。
第2図は、本発明方法を実施するための他のめ
つき装置の一例を示す図である。本例は基本的に
は第1図に示す装置と同様であるが、マスキング
バーナ21が酸化炉19と還元炉22との間に設
けられたスロート20に設置され、デフレクタロ
ーラ7、プリコートローラ8、およびターンロー
ラ11が省略されている点が異なつている。鋼帯
1はリバースローラ17によつて固形成分を溶解
した溶液18が塗布された後、酸化炉19を経て
スロート20に導かれ、マスキングバーナ21に
よつて非めつき側、すなわち乾燥状態の第1被覆
層上にすすが被覆される。次いで鋼帯1は還元炉
22、めつき浴24、合金化処理装置26、冷却
装置27、およびブラツシングローラ28に順次
導入される。本例では還元炉22の一端部がめつ
き浴24内の溶融金属中に浸漬されているので、
鋼帯1のめつき面が溶融金属中に浸漬される直前
で大気中に露出されないから酸化防止に効果があ
る。
第3図は、本発明方法を実施するための更に他
のめつき装置を示す図である。既に脱脂、酸洗に
よりその表面を清浄にされた鋼帯1は、めつき面
にフラツクス29をフラツクスコータ30により
塗布される。フラツクスは鋼帯の表面の不純物お
よび酸洗後に発生する極く軽微な酸化膜を除去す
るためのもので、例えば塩化亜鉛と塩化アンモニ
ウムの混合水溶液を用いる。一方、鋼帯1のめつ
き不要面にはリバースコータ32により、固形成
分を溶解した溶液31が塗布され第1被覆層が形
成される。乾燥炉33において、鋼帯1面上のフ
ラツクス塗布層と第1被覆層がともに乾燥させら
れる。乾燥した第1の被覆層にマスキングバーナ
34から炭化水素の不完全燃焼炎を当てすすを被
覆する。次いで鋼帯1はデフレクタローラ35を
経てシンクローラ36によりめつき浴37中に導
かれる。めつき浴37を通過した後、鋼帯1は大
気中に引き上げられ、合金化処理装置38により
合金化処理される。
第1図に示した方法により亜鉛めつきを施した
結果を従来方法の例と比較して第1表に示す。
本発明を適用すると、めつき浴から鋼板が引き
上げられる時に溶融金属の引き上げを阻止できる
ため、めつき速度限界が200m/min以上と、従
来法に比べて大幅に向上する。また、2層めつき
防止膜のため合金化処理を行つてもめつき不要面
は全く酸化しないか、極めてわずかの酸化に抑え
られる。更に、鋼帯1の非めつき面に形成される
すすの被膜は、酸化炉を通過した鋼帯1に対して
形成できる。したがつて、すすの被膜が酸化炉で
その着火点以上の温度に達し、燃焼する事態が避
けられるので、酸化炉の温度条件等の制約が少な
く、高速化が可能となる。
[Industrial Application Field] The present invention relates to a plating method in which a steel strip is immersed in a molten metal plating bath after an anti-plating film is formed in advance on the non-plating surface of a steel strip. The present invention relates to a method for partially molten metal plating of a steel strip, in which only a portion of the steel strip is glazed, for example, on one side. [Prior Art] In order to impart corrosion resistance to a steel plate, various corrosion-resistant coatings are often formed on the surface of the steel plate. in this case,
It is common to form a corrosion-resistant film on both sides of a steel plate. However, in the case of steel plates for automobiles that are painted after plating, if the plated surface is painted, the sharpness of the image will be poor and the product value will be significantly reduced. In addition, for example, the weldability of galvanized steel sheets is determined by the fact that the difference between the melting point and boiling point of zinc is small and the thermal conductivity is large;
Further, it is not preferable because it tends to contaminate the electrode. As described above, imparting corrosion resistance to the surface of a steel plate and weldability and sharpness after painting have contradictory properties. For this reason, so-called single-sided plated steel plates are being used for automobile steel plates and the like, in which only one side of the steel plate is plated to provide corrosion resistance, and the other side has paintability and weldability. [Problems to be Solved by the Invention] Methods for producing single-sided galvanized steel sheets by molten metal plating, such as hot-dip galvanizing, include a method of forming an anti-plating film on the non-plating surface of the steel sheet, and a method of forming an anti-plating film on the surface of the steel sheet that does not require plating, Alternatively, there is a method in which molten zinc is mechanically brought into contact with only one side of the steel plate using a roll or the like, or a method in which zinc on one side is removed by grinding after both sides are plated.
Among these methods, the mechanical method is technically difficult and therefore impractical, and the method of removing zinc on one side by grinding has the drawback of high cost. For these reasons, various methods have been proposed for forming an anti-plating film on surfaces that do not require plating, and known anti-plating agents include water glass, silicone resin, oxide film, alumina, and carbon. Among these anti-glazing agents, carbon generated by incomplete combustion of hydrocarbon fuel, so-called soot, does not react with molten zinc and has very low wettability.
Very high anti-stick performance. Also, soot is self-lubricating and the coefficient of friction of the soot surface is small, so when the steel strip is pulled out of the plating bath at high speed, the amount of molten zinc lifted up is extremely small. However, since soot is porous, even if a soot-preventing film is formed on the surface of the steel strip, oxygen from the atmosphere will enter the surface of the steel strip through this film. For this reason, after melt plating,
There is a drawback that the non-plated surface is oxidized, and in particular, when alloying is performed after plating, the oxidation progresses more rapidly since it is heated to about 500°C. On the other hand, anti-glazing materials other than soot have the drawback of simultaneously pulling up molten zinc when the steel strip is pulled out of the plating bath at high speed. [Object of the Invention] An object of the present invention is to eliminate the drawbacks of the prior art described above and to provide a plating method for producing high-quality partially hot-dip galvanized steel strip at high speed. [Means for Solving the Problems] The present invention provides a method for forming a plating prevention film containing carbon powder on the non-plating surface of a steel strip, and then immersing the steel strip in a molten metal plating bath. In the molten metal plating method, a coating film of a solution in which solid components are dissolved in advance is formed on the surface that does not require plating, and then this coating film is dried to form a layer that suppresses or substantially prevents the intrusion of oxygen. , is characterized by forming an anti-plating film containing carbon on the coating film. [Function] The composite (two-layer) anti-plating film according to the present invention will be described in further detail. The first coating layer is formed on the non-plating surface of the steel plate by applying a solution containing dissolved solid components to the non-plating surface of the steel plate by a method such as roll coating or spraying. As the solution in which the solid component is dissolved, an inorganic solution or a synthetic resin solution is used. In particular, materials with excellent heat resistance are desirable; for example, water glass, alumina, borax aqueous solution, silicone resin varnish, or silicone rubber varnish are most useful. It is especially desirable that the water glass is made by diluting a concentrated aqueous solution of alkali silicate salts with water, which is usually called a stock solution, and its concentration is such that it does not interfere with the application work.
The concentration is appropriately selected so that good adhesion can be obtained and a dense film can be formed after drying or vitrification by heat treatment. A general guideline is 0.1 to 30% by weight, preferably 0.5 to 20% by weight.
It is. In the case of synthetic resin varnish or borax aqueous solution, the concentration is selected depending on the type of resin, but as in the case of water glass, it should be selected appropriately so that a dense film can be formed with good workability. What is important for a coating film made of a solution containing dissolved solid components is that the film be sufficiently thick or dense so as to prevent oxygen from penetrating the surfaces of the steel strip that do not require plating as much as possible. Preventing the intrusion of oxygen can prevent oxidation of surfaces not to be plated during the heat alloying treatment after completion of plating, which is extremely convenient. Coating film of solution in which solid components are dissolved (first coating layer)
After substantially drying, an anti-plating film containing carbon powder is formed thereon. There is no need to install a special drying oven for drying the coating film made from a solution containing dissolved solid components, but it can be carried out using an oxidation oven or a drying oven for drying the flux applied to the steel strip. Just do it. Carbon powder can be used in either fixed or amorphous form. If the particle size of the carbon powder is too large, the contact area with the first coating layer will decrease and the adhesion will deteriorate, so it is preferable that the particle size is as small as possible. For practical purposes, a thickness of several μm or less is sufficient. The second film layer, the anti-plating film of carbon powder, is formed by spraying or roll coating. The most desirable method is to incompletely combust the hydrocarbons, blow the combustion flame directly onto the first coating layer, and attach the generated soot, which will improve adhesion, particle size of the powder, and conversion of the first coating layer into a solid phase. This is advantageous in terms of promoting If a dense first coating layer with high adhesion is formed after conversion to a solid phase and the intrusion of oxygen is suppressed or prevented, surfaces not to be plated will be oxidized even through alloying heat treatment, etc. High quality single-sided plated steel sheet can be obtained. In carrying out the method of the present invention, the following plating apparatus is used. That is, the apparatus for partially molten metal plating of a steel strip for carrying out the method of the present invention is an apparatus for forming a coating film of a solution containing solid components on the surface of the steel strip that does not require plating, and an apparatus for partially molten metal plating of a steel strip, which is an apparatus for forming a coating film of a solution containing solid components on the surface of the steel strip that does not need to be plated, and an apparatus for partially molten metal plating of a steel strip. After that, it is equipped with a device for forming an anti-plating film containing carbon powder on the coating film, a molten metal plating bath, and a device for removing solid components and carbon powder on the non-plated surface of the steel strip. [Example] The following plating method of the present invention will be explained in more detail with reference to the drawings. 1 to 3 are schematic diagrams showing a plating apparatus for carrying out the method of the present invention. First, in FIG. 1, a solution 2 in which a solid component is dissolved, such as water glass, is coated on the non-plating surface of a steel strip 1 using a reverse coater 3.
form a coating layer. The steel strip 1 then enters an oxidation furnace 4 while this first coating layer is substantially wet.
In the oxidation furnace 4, oil and the like adhering to the plated surface of the steel strip are burned and the first adhered layer is dried. The steel strip 1 that has passed through the oxidation furnace 4 passes through the throat 5 and then enters the reduction furnace 6. In the reduction furnace 6, oxides on the plated surface of the steel strip are reduced and cleaned. Next, the direction of movement of the steel strip 1 is changed by a deflector roller 7, and then a plating metal 9 is precoated on the plating surface side by a precoat roller 8 placed in a reducing atmosphere. This pre-coating is a process to prevent the plated surface of the steel strip from spewing out into the atmosphere.
On the other hand, the masking burner 10 coats soot on the non-plated side, that is, on the first coating layer. Hydrocarbons such as propane, butane, acetylene, natural gas, etc., and oxygen or air are supplied to the masking burner 10, and when the ratio thereof is adjusted appropriately,
Soot is generated efficiently from the combustion flame. Hydrocarbons with a high carbon element content are particularly desirable, and acetylene gas is effective. On the other hand, propane gas or butane gas has the advantage that carbon powder with fine particles can be obtained and a dense film can be formed. This combustion flame is blown onto the first coating layer to form a soot film, which serves as an anti-plating film. Thereafter, the steel strip 1 is changed in its traveling direction by a turn roller 11, immersed in molten metal 9 in a plating bath 12, and drawn out into the atmosphere via a sink roller 13. At this time, since the non-plated surface of the steel strip 1 is coated with soot and a first coating layer that substantially prevents oxygen from entering, oxidation of the non-plated surface by oxygen in the atmosphere will proceed. There is no or only slight
Further, the molten metal 9 is prevented from being pulled up at the same time. Next, the steel strip 1 enters the alloying furnace 14 and is again held at a high temperature, for example, about 500° C. for galvanizing, for 10 to 60 seconds to improve its material quality. Even at such high temperatures, the two-layer coating prevents oxidation of surfaces that do not require plating. Alloying treatment may or may not be necessary depending on the use of the plated steel strip. After the steel strip 1 is cooled to about room temperature by a cooling device 15, the two-layer coating on the non-plated surface, that is, the carbon powder and other solid components, is ground away by a brushing roll 16, and a single-sided plated steel strip is obtained. It will be done. FIG. 2 is a diagram showing an example of another plating apparatus for carrying out the method of the present invention. This example is basically the same as the apparatus shown in FIG. , and that the turn roller 11 is omitted. After the steel strip 1 is coated with a solution 18 in which solid components are dissolved by a reverse roller 17, it is guided through an oxidation furnace 19 to a throat 20, and is heated to the non-plated side, that is, the dry side, by a masking burner 21. Soot is coated onto one coating layer. Next, the steel strip 1 is sequentially introduced into a reduction furnace 22, a plating bath 24, an alloying treatment device 26, a cooling device 27, and a brushing roller 28. In this example, one end of the reduction furnace 22 is immersed in the molten metal in the plating bath 24.
Since the plated surface of the steel strip 1 is not exposed to the atmosphere immediately before being immersed in the molten metal, it is effective in preventing oxidation. FIG. 3 is a diagram showing still another plating apparatus for carrying out the method of the present invention. The surface of the steel strip 1, whose surface has already been cleaned by degreasing and pickling, is coated with flux 29 by a flux coater 30 on the plating surface. Flux is used to remove impurities on the surface of the steel strip and a very slight oxide film generated after pickling. For example, a mixed aqueous solution of zinc chloride and ammonium chloride is used. On the other hand, a solution 31 in which solid components are dissolved is applied by a reverse coater 32 to the surface of the steel strip 1 that does not require plating, thereby forming a first coating layer. In the drying oven 33, both the flux coating layer and the first coating layer on the surface of the steel strip are dried. The dry first coating layer is exposed to an incomplete combustion flame of hydrocarbon from a masking burner 34 to coat the soot. The steel strip 1 is then led via a deflector roller 35 into a plating bath 37 by a sink roller 36. After passing through the plating bath 37, the steel strip 1 is taken up into the atmosphere and alloyed by an alloying treatment device 38. The results of galvanizing using the method shown in FIG. 1 are shown in Table 1 in comparison with the conventional method. When the present invention is applied, it is possible to prevent the molten metal from being pulled up when the steel plate is pulled up from the plating bath, so the plating speed limit is 200 m/min or more, which is significantly improved compared to the conventional method. In addition, since it is a two-layer anti-plating film, even if alloying treatment is performed, the surfaces that do not require plating will not be oxidized at all or will only be oxidized to a very small extent. Furthermore, the soot film formed on the non-plated surface of the steel strip 1 can be formed on the steel strip 1 that has passed through the oxidation furnace. Therefore, it is possible to avoid a situation in which the soot film reaches a temperature higher than its ignition point in the oxidation furnace and burns, so there are fewer restrictions on the temperature conditions of the oxidation furnace, and higher speeds are possible.
本発明によれば、高品質の部分溶融めつき鋼帯
を高速に製造するめつき方法が得られる。
According to the present invention, a plating method for manufacturing high-quality partially hot-dip galvanized steel strip at high speed is provided.
第1図〜第3図は本発明の方法を適用すべくめ
つき装置の概略を示す図である。
1…鋼帯、2,18,31…固形成分を溶解し
た溶液、3,17,30,31…リバースコー
タ、4,19…酸化炉、5,20…スロート、
6,22…還元炉、7,23,35…デフレクタ
ーローラ、8…プリコートローラ、9…溶融金
属、10,21,34…マスキングバーナ、11
…ターンローラ、12,24,37…めつき浴、
13,25,36…シンクローラ、14,26,
38…合金化処理装置、15,27…冷却装置、
16,28…ブラツシングローラ、29…フラツ
クス、30…フラツクスコータ。
1 to 3 are diagrams schematically showing a plating apparatus to which the method of the present invention is applied. 1... Steel strip, 2, 18, 31... Solution in which solid components are dissolved, 3, 17, 30, 31... Reverse coater, 4, 19... Oxidation furnace, 5, 20... Throat,
6, 22... Reduction furnace, 7, 23, 35... Deflector roller, 8... Precoat roller, 9... Molten metal, 10, 21, 34... Masking burner, 11
...Turn roller, 12, 24, 37...Plating bath,
13, 25, 36...Sync roller, 14, 26,
38... Alloying treatment device, 15, 27... Cooling device,
16, 28...Brushing roller, 29...Flux, 30...Flux coater.
Claims (1)
つき防止膜を形成し、その後鋼帯を溶融金属めつ
き浴に浸漬する鋼帯の部分溶融金属めつき方法に
おいて、めつき不要面に、予め固形成分を溶解し
た溶液の塗膜を形成し、次にこの塗膜を乾燥させ
酸素の侵入を抑制または実質的に阻止する層とし
た後、塗膜上にカーボンを含むめつき防止膜を形
成することを特徴とする鋼帯の部分溶融金属めつ
き方法。 2 特許請求の範囲第1項において、固形成分を
溶解した溶液が、水ガラス、アルミナ、およびホ
ウ砂水溶液の少なくとも1種であることを特徴と
する鋼帯の部分溶融金属めつき方法。 3 特許請求の範囲第1項または第2項におい
て、固形成分を溶解した溶液が、合成樹脂の溶液
であることを特徴とする鋼帯の部分溶融金属めつ
き方法。 4 特許請求の範囲第3項において、合成樹脂が
シリコーン樹脂、シリコーンゴム、および熱可塑
性樹脂から選ばれるものであることを特徴とする
鋼帯の部分溶融金属めつき方法。 5 上記特許請求の範囲第1項から第4項のいず
れか一項において、カーボン粉末を含むめつき防
止膜を炭化水素の不完全燃焼により生じたカーボ
ンで形成することを特徴とする鋼帯の部分溶融金
属めつき方法。[Scope of Claims] 1. A method for partially molten metal plating of a steel strip, in which a plating prevention film containing carbon powder is formed on the non-plating surface of the steel strip, and then the steel strip is immersed in a molten metal plating bath, A coating film of a solution in which solid components are dissolved in advance is formed on the surface that does not need plating, and then this coating film is dried to form a layer that suppresses or substantially prevents the intrusion of oxygen, and then carbon is applied on the coating film. 1. A method for partially molten metal plating of a steel strip, the method comprising forming an anti-plating film comprising: 2. The method for partially molten metal plating of a steel strip according to claim 1, wherein the solution in which the solid component is dissolved is at least one of water glass, alumina, and a borax aqueous solution. 3. The method for partially molten metal plating of a steel strip according to claim 1 or 2, wherein the solution in which the solid component is dissolved is a solution of a synthetic resin. 4. The method for partially molten metal plating of a steel strip according to claim 3, wherein the synthetic resin is selected from silicone resin, silicone rubber, and thermoplastic resin. 5. The steel strip according to any one of claims 1 to 4 above, characterized in that the anti-plating film containing carbon powder is formed of carbon produced by incomplete combustion of hydrocarbons. Partially molten metal plating method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55119815A JPS5747855A (en) | 1980-09-01 | 1980-09-01 | Method and device for partial metal hot dipping of steel strip |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55119815A JPS5747855A (en) | 1980-09-01 | 1980-09-01 | Method and device for partial metal hot dipping of steel strip |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5747855A JPS5747855A (en) | 1982-03-18 |
| JPS6115946B2 true JPS6115946B2 (en) | 1986-04-26 |
Family
ID=14770916
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55119815A Granted JPS5747855A (en) | 1980-09-01 | 1980-09-01 | Method and device for partial metal hot dipping of steel strip |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5747855A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04178010A (en) * | 1990-11-13 | 1992-06-25 | Nec Eng Ltd | Clock generating circuit |
-
1980
- 1980-09-01 JP JP55119815A patent/JPS5747855A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5747855A (en) | 1982-03-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP4137793B2 (en) | Method for coating a metal surface | |
| FI90668B (en) | Method of coating a steel sheet with aluminum | |
| JP5600868B2 (en) | Method for producing molten Al-Zn plated steel sheet | |
| JPS62274060A (en) | Molten aluminum coated chromium alloy steel | |
| US4584211A (en) | Continuous hot dip aluminum coating method | |
| JP2768871B2 (en) | Melt coating method for chromium-containing steel | |
| JPS5915980B2 (en) | Method for producing thick pure aluminum coating on small diameter pipe material | |
| CA1069390A (en) | Method for effecting one side molten metal coating | |
| JPS6115946B2 (en) | ||
| JPS6115945B2 (en) | ||
| JPS58110664A (en) | Partial metal hot dipping method for steel strip | |
| JPS6115947B2 (en) | ||
| US3089780A (en) | Method and composition for shielding steel from molten coating metal | |
| KR100928805B1 (en) | Manufacturing method of alloyed hot-dip galvanized steel sheet with beautiful surface | |
| US3177053A (en) | Differentially coated galvanized strip | |
| JP2011177621A (en) | Method of manufacturing surface-treated coated steel sheet | |
| KR840001260B1 (en) | Hot dip metal plating method | |
| JPS6135266B2 (en) | ||
| JPS61243162A (en) | Production of al series hot dipped steel plate excellent in heat resistance | |
| KR100338351B1 (en) | Manufacturing method of zinc-titanium colored hot dip galvanized steel sheet | |
| JPS6049713B2 (en) | Single-sided melt plating method for steel plate | |
| CA1137361A (en) | Molten metal plating method and apparatus and plating preventing agent therefor | |
| JP2000054096A (en) | Roll member for hot-dip metal coating bath, and its production | |
| JPS5837163A (en) | Alloying treatment method of galvanized steel plate | |
| JP4517683B2 (en) | Method for producing hot-dip plated plate |