JPH01116085A - Formation of insulating coat having superior suitability to blanking and welding on electrical steel sheet - Google Patents
Formation of insulating coat having superior suitability to blanking and welding on electrical steel sheetInfo
- Publication number
- JPH01116085A JPH01116085A JP27040887A JP27040887A JPH01116085A JP H01116085 A JPH01116085 A JP H01116085A JP 27040887 A JP27040887 A JP 27040887A JP 27040887 A JP27040887 A JP 27040887A JP H01116085 A JPH01116085 A JP H01116085A
- Authority
- JP
- Japan
- Prior art keywords
- steel sheet
- resin
- welding
- roll
- electrical steel
- 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
- 229910000976 Electrical steel Inorganic materials 0.000 title claims abstract description 10
- 238000003466 welding Methods 0.000 title abstract description 16
- 230000015572 biosynthetic process Effects 0.000 title description 2
- 229920005989 resin Polymers 0.000 claims abstract description 35
- 239000011347 resin Substances 0.000 claims abstract description 35
- 230000003746 surface roughness Effects 0.000 claims abstract description 16
- 239000000839 emulsion Substances 0.000 claims abstract description 10
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 8
- 239000007788 liquid Substances 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 23
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 5
- 239000010452 phosphate Substances 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 claims 1
- 229920003002 synthetic resin Polymers 0.000 claims 1
- 239000000057 synthetic resin Substances 0.000 claims 1
- 229910000831 Steel Inorganic materials 0.000 abstract description 29
- 239000010959 steel Substances 0.000 abstract description 29
- 235000021317 phosphate Nutrition 0.000 abstract description 7
- 239000004925 Acrylic resin Substances 0.000 abstract description 3
- 229920000178 Acrylic resin Polymers 0.000 abstract description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 abstract description 3
- 150000003839 salts Chemical class 0.000 abstract description 3
- 229910052782 aluminium Inorganic materials 0.000 abstract description 2
- 229910052791 calcium Inorganic materials 0.000 abstract description 2
- 229910052725 zinc Inorganic materials 0.000 abstract description 2
- 230000001105 regulatory effect Effects 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 238000000576 coating method Methods 0.000 description 14
- 239000000463 material Substances 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 7
- 239000011146 organic particle Substances 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 238000004080 punching Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 229920000180 alkyd Polymers 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 3
- 239000011324 bead Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 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
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 229920003090 carboxymethyl hydroxyethyl cellulose Polymers 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- GIOZLVMCHDGNNZ-UHFFFAOYSA-N magnesium;oxido-(oxido(dioxo)chromio)oxy-dioxochromium Chemical compound [Mg+2].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O GIOZLVMCHDGNNZ-UHFFFAOYSA-N 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000011163 secondary particle Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000004846 water-soluble epoxy resin Substances 0.000 description 1
- 239000011701 zinc 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
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/73—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals characterised by the process
- C23C22/74—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals characterised by the process for obtaining burned-in conversion coatings
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Treatment Of Metals (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は、電磁鋼板の表面に打抜性、溶接性および電気
絶縁性の優れた絶縁皮膜を形成する方法に関するもので
ある。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a method for forming an insulating film with excellent punchability, weldability and electrical insulation properties on the surface of an electrical steel sheet.
〈従来の技術〉
家電用のモーターやトランスの鉄心は、電磁鋼板を所定
の形状に連続打抜し、ついでそれらを多数積層してその
側面をTIG溶接し組立てられる。<Prior Art> Iron cores for motors and transformers for home appliances are assembled by continuously punching electromagnetic steel plates into a predetermined shape, then stacking a large number of them and TIG welding the sides.
従って、電磁調板には打抜性と溶接性が優れていること
が同時に要求される。Therefore, electromagnetic control plates are required to have excellent punchability and weldability at the same time.
電磁鋼板の打抜性および溶接性は鋼板自体の材質もさる
ことながら、その表面に処理した絶縁皮膜の組成や膜厚
に大きく左右されることが知られている。It is known that the punchability and weldability of electromagnetic steel sheets depend not only on the material of the steel sheet itself, but also on the composition and thickness of the insulating film treated on its surface.
現在実用化されている絶縁皮膜を組成的に大別すると、
(A)無機質系(リン酸塩、クロム酸塩、重クロム酸塩
等)
(B)半有機賞系(クロム酸塩、樹脂系等)および
(C)有機質系(樹脂、フェス等)の3種類になる。The insulating films currently in practical use can be roughly classified based on their composition: (A) Inorganic (phosphate, chromate, dichromate, etc.) (B) Semi-organic (chromate, resin, etc.) etc.) and (C) organic type (resin, festival, etc.).
ところで無機質系(A)の皮膜を施した電磁鋼板はTI
G溶接溶接ロブローホール生がなく、溶接性がすぐれて
いるが、打抜金型の1回研磨当りの打抜回数は約10万
回程度で、打抜性が悪い。By the way, the electrical steel sheet coated with an inorganic (A) film is TI.
G welding There is no welding lobe hole formation, and the weldability is excellent, but the number of punches per polishing of the punching die is about 100,000, and the punching performance is poor.
一方、半有機賞系(B)および有機質系(C)の皮膜の
場合は、約150万回ものすぐれた打抜が得られる反面
、溶接時に樹脂等の分解によりガスを発生し、ブローホ
ールを生じ易く溶接性が劣る。On the other hand, in the case of semi-organic type (B) and organic type (C) coatings, excellent punching performance of about 1.5 million times can be obtained, but on the other hand, gas is generated due to decomposition of resin etc. during welding, and blowholes occur. This occurs easily and the weldability is poor.
このような半有機賞系および有機質系皮膜の溶接性を向
上させるため、皮膜表面に粗度を与える技術思想が特公
昭49−19078号に提示されている。In order to improve the weldability of such semi-organic and organic coatings, a technical concept for imparting roughness to the coating surface was proposed in Japanese Patent Publication No. 49-19078.
その粗度の与え方として、有機皮膜を均一に塗布し、焼
付中の未硬化皮膜にあらさを有するロールで処理する方
法、ミゾ切り塗布ロールで鋼板表面に縦ミゾ皮膜を形成
し、次いでは焼付中の未硬化皮膜にミゾ切りスチールロ
ールで横ミゾを入れる方法、処理液中に約2μm以上の
有機物粒子を添加して塗布焼付る方法などが開示されて
いる。The roughness can be achieved by applying an organic film uniformly and treating the uncured film during baking with a roll that has roughness, or by forming a vertically grooved film on the surface of the steel plate with a grooved coating roll, and then baking. A method is disclosed in which horizontal grooves are formed in the uncured film inside using a grooved steel roll, and a method in which organic particles of approximately 2 μm or more are added to the treatment solution and applied and baked.
この中で、最も工業的に有効な方法は最後の有機物粒子
を処理液中に添加し、塗布焼付る方法であるが、有機物
粒子を添加するのみでは分散性や鋼板への付着性(密着
性)に問題があった。Among these methods, the most industrially effective method is to add the last organic particles to the treatment solution and apply and bake. ) had a problem.
この有機物粒子の処理液中での分散に問題があると、長
時間安定して所定の表面粗さを有する絶縁皮膜が形成さ
れず、また有機物粒子が凝集した2次粒子状となって有
機物粒子の鋼板への付着性(密着性)が悪くなり、絶縁
皮膜を有する!磁鋼板をスリットするさい、テンツシ町
ンバット等での鋼板の締付けによって有機物粒子が剥離
する欠点を有していた。If there is a problem with the dispersion of these organic particles in the processing solution, an insulating film that is stable for a long time and has a specified surface roughness will not be formed, and the organic particles will aggregate into secondary particles. The adhesion (adhesion) to the steel plate becomes poor and there is an insulating film! When slitting a magnetic steel sheet, it has the disadvantage that organic particles come off due to the tightening of the steel sheet with a mechanical batt or the like.
この欠点を解決し、有機物粒子の分散性および鋼板への
付着性向上を図る技術が特公昭55−21111号公報
で提案された。A technique for solving this drawback and improving the dispersibility of organic particles and their adhesion to steel sheets was proposed in Japanese Patent Publication No. 55-21111.
これは有機樹脂粒子を予めエマルジ四ン樹脂溶液に添加
し、均一分散させた後に塗布液へ混合する方法であるが
、未だ有機樹脂粒子の処理液中での分散状態が完全でな
いことから、その改善法が特公昭61−183479号
で提案されている。This is a method in which organic resin particles are added to the emulsion resin solution in advance, uniformly dispersed, and then mixed into the coating solution. However, since the organic resin particles are not yet completely dispersed in the processing solution, An improvement method is proposed in Japanese Patent Publication No. 183479/1983.
これは、有機樹脂粒子をエマルジョン樹脂溶液へ添加す
る前に分散性向上剤で表面処理することを特徴としてい
るが、未だ処理液中での有機樹脂の分散性は不十分なも
のであった。This method is characterized by surface treating the organic resin particles with a dispersibility improver before adding them to the emulsion resin solution, but the dispersibility of the organic resin in the treatment liquid is still insufficient.
この分散性が悪いと、前記した如く、有機樹脂粒子が2
次粒子状となり有機物粒子の鋼板への付着性(密着性)
を劣化させる。さらに、有機樹脂粒子と処理液は異質の
ものであ°す、処理液中へ充分に分散しても、鋼板への
塗布作業中は浮上あるいは沈降を防止するため常に撹拌
が必要となる。If this dispersibility is poor, as mentioned above, the organic resin particles
Adhesion of organic particles to the steel plate (adhesion)
deteriorate. Furthermore, the organic resin particles and the treatment liquid are different, so even if they are sufficiently dispersed in the treatment liquid, constant stirring is required to prevent floating or sedimentation during application to a steel plate.
また、有機樹脂粒子混合処理液を配管輸送すると、有機
樹脂粒子の浮上あるいは沈降により配管づまりを起こし
、作業上大きな問題となっている。Furthermore, when a treatment liquid mixed with organic resin particles is transported through a pipe, the floating or settling of the organic resin particles causes the pipe to become clogged, which poses a major operational problem.
〈発明が解決しようとする問題点〉
本発明は有機樹脂の分散性を改善し、打抜性および溶接
性の優れた半有機賞系ないし有機質系の電磁鋼板の絶縁
皮膜の形成方法を提供するのである。<Problems to be Solved by the Invention> The present invention provides a method for forming an insulating film on a semi-organic or organic electromagnetic steel sheet that improves the dispersibility of an organic resin and has excellent punchability and weldability. It is.
〈問題解決のための手段〉
本発明は、電磁鋼板の表面に夫々の粘度を300゜〜5
000cpに調整した、リン酸塩系、クロム酸塩系、お
よび重クロム酸塩系の一種以上の処理液と有機樹脂とを
混合した処理液、あるいは水溶性樹脂、あるいはエマル
ジ四ン樹脂のいずれかの皮膜処理液をグラビアロールを
ピックアップロールとしたナチュラル・リバース方式で
塗布し、次いで焼付は処理を行ない表面粗さをRaで0
.5〜1.5μmとすることを特徴とする打抜性および
溶接性の優れた電磁鋼板の絶縁皮膜の形成方法である。<Means for solving the problem> The present invention provides a method of applying a viscosity of 300 to 5 on the surface of an electrical steel sheet.
A treatment solution that is a mixture of one or more phosphate-based, chromate-based, and dichromate-based processing solutions and an organic resin adjusted to 0.000 cp, a water-soluble resin, or an emulsion resin. The film treatment solution was applied using a natural reverse method using a gravure roll as a pick-up roll, and then baking was performed to reduce the surface roughness to 0 in Ra.
.. This is a method for forming an insulating film on an electrical steel sheet with excellent punchability and weldability, characterized by having a thickness of 5 to 1.5 μm.
〈作 用〉
本発明において用いる皮膜処理液は、リン酸塩系、クロ
ム酸塩系、重クロム酸塩系の1種以上の処理液と有機樹
脂とを混合した処理液、あるいは水溶性樹脂、あるいは
エマルジョン樹脂の処理液である。<Function> The coating treatment liquid used in the present invention is a treatment liquid that is a mixture of one or more phosphate-based, chromate-based, or dichromate-based treatment liquids and an organic resin, or a water-soluble resin, Alternatively, it is a treatment liquid for emulsion resin.
リン酸塩系、クロム酸塩系あるいは重クロム酸塩系の塩
としては、亜鉛、アルミニウム、カルシウム、マグネシ
ウムのリン酸塩、クロム酸塩、重クロム酸塩、または亜
鉛、アルミニウム、カルシウム、マグネシウムの酸化物
、水酸化物、炭酸塩をリン酸、無水クロム酸に溶解した
ものなどがあり、これらの2種以上を混合したものであ
ってもよい、この液に配合する有機樹脂としては、水溶
性またはエマルジョンタイプのアクリル樹脂およびその
共重合物、酢酸ビニル樹脂およびその共重合物、ブダジ
エンースチレン共重合物、アルキッド樹脂、エポキシ樹
脂またはその変性物等の1種または2種以上を用いる。Phosphate, chromate, or dichromate salts include phosphates, chromates, and dichromates of zinc, aluminum, calcium, and magnesium; These include oxides, hydroxides, and carbonates dissolved in phosphoric acid and chromic anhydride, and may also be a mixture of two or more of these. One or more of aqueous or emulsion type acrylic resins and their copolymers, vinyl acetate resins and their copolymers, butadiene-styrene copolymers, alkyd resins, epoxy resins, or modified products thereof are used.
還元剤として、エチレングリコールや、グリセリンなど
の多価アルコールを添加し、さらにコロイド状シリカ、
コロイド状アルミナ、硼酸等、耐熱性向上剤を添加して
も良い。As a reducing agent, polyhydric alcohol such as ethylene glycol or glycerin is added, and colloidal silica,
Heat resistance improvers such as colloidal alumina and boric acid may be added.
これら成分の添加量としては、リン酸塩、クロム酸塩等
の無機成分100111部に対して有a樹脂成分は5重
量部以上が好ましい、5重量部より少ないと充分な打抜
性が得られない。The amount of these components to be added is preferably 5 parts by weight or more for the aliphatic resin component per 100,111 parts of inorganic components such as phosphates and chromates; sufficient punchability is obtained when it is less than 5 parts by weight. do not have.
次にエチレングリコール等の還元剤は0.5〜30重量
部、硼酸等の耐熱性向上剤は0.5〜30重量部が適当
である。Next, it is appropriate to use a reducing agent such as ethylene glycol in an amount of 0.5 to 30 parts by weight, and a heat resistance improver such as boric acid in an amount of 0.5 to 30 parts by weight.
上記水溶性混合物の粘度は1.2〜3cpであり、塗布
方法としてピックアップロールにグラビアロールを用い
たナチュラルリバース方式を採用しても鋼板表面には、
均一に塗布され表面粗度Raはせいぜい0.15μm程
度までであり、本発明の目的である溶接性向上は認めら
れない。The viscosity of the above-mentioned water-soluble mixture is 1.2 to 3 cp, and even if the natural reverse method using a gravure roll as a pick-up roll is adopted as the application method, no coating will be applied to the steel plate surface.
It is applied uniformly, and the surface roughness Ra is at most about 0.15 μm, and the improvement in weldability, which is the objective of the present invention, is not observed.
溶接性向上には表面粗度Raは0.5〜1.5 μmで
なくてはならない、0.5Brn未満では溶接性が劣り
、また1、5μm以上ではスリット時のテンションパッ
トの接触で皮膜剥離が起こりやすく、さらに占積率が劣
化するため好ましくない0表面粗度Raを0.5μm以
上とするためには、上記処理液の粘度を上げる必要があ
る。To improve weldability, the surface roughness Ra must be between 0.5 and 1.5 μm. If it is less than 0.5 Br, weldability will be poor, and if it is more than 1.5 μm, the film will peel off due to contact with the tension pad during slitting. In order to increase the zero surface roughness Ra to 0.5 μm or more, it is necessary to increase the viscosity of the treatment liquid.
この粘度上昇のためには、カルボキシルメチルセルロー
スや、ヒドロキシエチルセルロースを配合すれば良い、
この配合量は、先の無機成分100部に対して、1〜3
0部が良い、1部より少ないと増粘硬化がなく30部よ
り多(配合すると、皮膜の密着性が劣化するためである
−
この増粘剤を配合することにより処理液粘度を300〜
5000cpに調整する。粘度が300cpより小さい
と所期の目的である表面粗度RaO,5,gmを確保す
ることが困難である。また、5000cp以上ではナチ
ュラルリバース方式の塗布方法では作業性が劣り経済的
でない。To increase this viscosity, carboxymethyl cellulose or hydroxyethyl cellulose can be added.
This blending amount is 1 to 3 parts per 100 parts of the above inorganic component.
0 parts is good; less than 1 part will not thicken and harden, and more than 30 parts (this is because the adhesion of the film will deteriorate if it is added.) By adding this thickener, the viscosity of the processing liquid can be increased from 300 to 300 parts.
Adjust to 5000cp. If the viscosity is less than 300 cp, it is difficult to secure the desired surface roughness RaO, 5, gm. Further, when the pressure is 5000 cp or more, the natural reverse coating method has poor workability and is not economical.
一方、分散系皮膜を処理液として用いる水溶性有機樹脂
としては、エポキシエステル、ポリエステル、メラミン
、ポリエチレン、ポリアクリル、アルキッド等の1種以
上が好適に使用でき、またエマルジョン樹脂としては、
アクリル樹脂およびその共電化合物、酢酸ビニルおよび
その共電化合物、ブタジェン−スチレン共重合物アルキ
ッド、エポキシまたはその変性物等の1種以上が好適に
使用できる。これらの水溶性有機樹脂、エマルジテン樹
脂は、増粘剤や界面活性剤などで粘度を300〜500
0cpに調整したものを用いる。On the other hand, as the water-soluble organic resin for which the dispersion film is used as a treatment liquid, one or more of epoxy ester, polyester, melamine, polyethylene, polyacrylic, alkyd, etc. can be suitably used, and as the emulsion resin,
One or more of acrylic resins and coelectric compounds thereof, vinyl acetate and coelectric compounds thereof, butadiene-styrene copolymer alkyds, epoxies, or modified products thereof can be suitably used. These water-soluble organic resins and emulditene resins have a viscosity of 300 to 500 using thickeners and surfactants.
Use one adjusted to 0 cp.
他方、塗布方法は、グラビアロールをピックアップロー
ルとしたナチュラル・リバースロール方式とする。On the other hand, the coating method is a natural reverse roll method using a gravure roll as a pickup roll.
グラビアロールとしては、そのグラビアの形状はピラミ
ッド型、格子型、斜線型など、いずれでも良い、これら
の線数や深度は処理液の濃度・粘度により選定される。As for the gravure roll, the shape of the gravure may be pyramid-shaped, lattice-shaped, oblique line-shaped, etc., and the number of lines and depth of these are selected depending on the concentration and viscosity of the processing liquid.
ナチュラルallをグラビアロールとゴムロールで行な
い、グラビアロールの形状およびサイズで塗布量が制限
される。このグラビアの凹部に入っている処理液の約半
分がゴムロール上に点状に転写される。ナチュラル・リ
バースクール方式とするためには、このゴムロール、す
なわちアプリケ−クロールを鋼板の進行方向とは逆回転
として、鋼板表面に点状処理液を転写すれば良い。Natural all is performed using a gravure roll and a rubber roll, and the amount of coating is limited by the shape and size of the gravure roll. Approximately half of the processing liquid contained in the gravure recesses is transferred onto the rubber roll in a dotted manner. In order to use the natural reverse cooling method, the rubber roll, that is, the applicator roll, may be rotated in the opposite direction to the advancing direction of the steel plate to transfer dots of the treatment liquid onto the surface of the steel plate.
この状態をもって、通常の乾燥、焼付を施すことにより
、鋼板表面にRaが0.5〜1.5 μmの絶縁皮膜を
得ることができる。By performing normal drying and baking in this state, an insulating film having an Ra of 0.5 to 1.5 μm can be obtained on the surface of the steel plate.
〈実 施 例〉
実施例 1
電磁調板(Sf j 0.35%、板厚0.5mm、板
幅1G25am、表面粗さRaO,18μm)の表面に
後記の処理液A(粘度320cρ)をピックアップロー
ルに格子型のグラビアロール(I35メツシュ、線数3
5、深度0.22m−)を用いナチユラル・リバース方
式にて塗布し、500℃で60秒間焼付けた。得られた
皮膜の目付量は6.5g/rdで皮膜の表面粗度Raは
0.62mmであった。<Example> Example 1 The treatment liquid A (viscosity 320cρ) described below was picked up on the surface of an electromagnetic control plate (Sf j 0.35%, plate thickness 0.5mm, plate width 1G25am, surface roughness RaO, 18μm). Grid type gravure roll (I35 mesh, number of lines 3)
5, depth of 0.22 m-) using the natural reverse method and baked at 500°C for 60 seconds. The area weight of the obtained film was 6.5 g/rd, and the surface roughness Ra of the film was 0.62 mm.
本皮膜を有する鋼板を積層し、TIG溶接したところ、
電流120Aで100cm/分の溶接速度でもブローホ
ールの発生はなく、美麗なビードが得られた0本材料を
20−l−のスチールダイス(クリアランス6%)で打
抜いたところ、カエリ高さ50μmまでに180万回打
抜けた。When steel plates with this film were laminated and TIG welded,
Even at a current of 120 A and a welding speed of 100 cm/min, there were no blowholes and a beautiful bead was obtained. When the material was punched with a 20-l steel die (clearance 6%), the burr height was 50 μm. To date, he has hit the ball 1.8 million times.
比較例 l
比較材として、実施例1と同一材種の綱板に処理液Aを
ピックアップロールにフラットロールを用いナチュラル
・リバース方式にて塗布し、500℃で60秒間焼付け
た。得られた皮膜の目付量は、6.2g/ldで皮膜の
表面粗度Raは0.211℃mであった。Comparative Example 1 As a comparative material, treatment liquid A was applied to a steel plate of the same material type as in Example 1 using a natural reverse method using a flat roll as a pick-up roll, and baked at 500° C. for 60 seconds. The area weight of the obtained film was 6.2 g/ld, and the surface roughness Ra of the film was 0.211° C.m.
この皮膜を有する鋼板の打抜きは、上記同様の条件で実
施したところ、カエリ高さ50μmまでに210万回打
抜けた。しかし、実施例1と同様の条件でTIG溶接し
たところ、ブローホールがビード全体に多数発生した。When the steel plate having this film was punched under the same conditions as above, it was punched 2.1 million times until the burr height was 50 μm. However, when TIG welding was performed under the same conditions as in Example 1, many blowholes were generated throughout the bead.
比較例 2
さらに比較材として処理液B(粘度1.8cp)を実施
例1と同様にピックアップロールに格子型グラビアロー
ル(I35メッシェ、線数35、深度0.22■)を用
いナチュラル・リバース方式にて塗布し、500℃で6
0秒間焼付けた。得られた皮膜の目付量は6.6g/M
で皮膜の表面粗度Raは0.24μmであった。Comparative Example 2 Further, as a comparison material, processing liquid B (viscosity 1.8 cp) was used in the same manner as in Example 1 using a lattice type gravure roll (I35 mesh, number of lines 35, depth 0.22 ■) as a pick-up roll and a natural reverse method. 6 at 500℃.
Baked for 0 seconds. The area weight of the obtained film was 6.6g/M
The surface roughness Ra of the film was 0.24 μm.
この皮膜を有する鋼板を積層し、TIG溶接したところ
、電流120Aで20C11/分の溶接速度でブローホ
ールの発生は認められなかったが、それ以上の溶接速度
ではブーローホールの発生がある。When steel plates having this coating were laminated and TIG welded, no blowholes were observed at a welding speed of 20C11/min at a current of 120A, but at higher welding speeds, blowholes occurred.
・30%重クロム酸マグネシウム溶液 130部(無
機成分 41部)
・アクリル−酢酸ビニル樹脂エマルジョン(樹脂固形分
50%)30部
・エチレングリコール 10部・カル
ボキシルメチルセルロース 10部〔処理液B〕
処理[Aのカルボキシルメチルセルロースを除いたもの
(従来のクロム酸塩−有機樹脂系処理液)他の皮膜緒特
性は表1に示す。・30% magnesium dichromate solution 130 parts (inorganic component 41 parts) ・Acrylic-vinyl acetate resin emulsion (resin solid content 50%) 30 parts ・Ethylene glycol 10 parts ・Carboxyl methyl cellulose 10 parts [Treatment liquid B] Treatment [A] Table 1 shows the properties of other films excluding the carboxymethylcellulose (conventional chromate-organic resin treatment solution).
実施例2
電磁鋼板(St:3.1%、板厚0.5m+e、板幅9
401、表面粗さRa O,23μm)の表面に処理液
C(粘度1800cp )をピックアップロールにピラ
ミッド型のグラビアロール(#32メッシェ、線数32
、深度0.26m5+)を用いナチュラル・リバース方
式にて塗布し、450℃で60秒間焼付けた。得られた
皮膜の目付量は7.2g/n(で皮膜の表面粗度Raは
0.76μmであった。Example 2 Electromagnetic steel plate (St: 3.1%, plate thickness 0.5m+e, plate width 9
401, surface roughness Ra O, 23 μm), treatment liquid C (viscosity 1800 cp) was applied to a pyramid-shaped gravure roll (#32 mesh, number of lines 32) using a pickup roll.
, depth 0.26m5+) using the natural reverse method and baked at 450°C for 60 seconds. The area weight of the obtained film was 7.2 g/n (and the surface roughness Ra of the film was 0.76 μm).
本皮膜を有する鋼板を積層し、TIG溶接したところ、
電流12OAで120CI/分の溶接速度でもブローホ
ールの発生はなく美しいビード得られた。When steel plates with this film were laminated and TIG welded,
Even at a current of 12 OA and a welding speed of 120 CI/min, a beautiful bead was obtained with no blowholes.
この材料の打抜性(2〇−霞φのスチールダイス、クリ
アランス6%)は、カエリ高さ50μまでの打抜数で7
2%回であった。The punching performance of this material (20 - Kasumi φ steel die, clearance 6%) is 7 in the number of punches up to a burr height of 50μ.
It was 2% of the time.
比較例3
比較材として、実施例2と同一材種の鋼板に処理液D(
粘度160cp )を実施例2と同一条件で塗布したと
ころ、得られた皮膜の目付量は6.8 g/イであり、
表面粗度Raは0.38μmであった。Comparative Example 3 As a comparative material, treatment liquid D (
When a film with a viscosity of 160 cp) was applied under the same conditions as in Example 2, the area weight of the obtained film was 6.8 g/I,
The surface roughness Ra was 0.38 μm.
この材料を710℃接したところ、ブローホールの発生
しない溶接速度は30C11/分であり、205mφの
スチールダイスでの打抜性(カエリ高さ50部mまでの
打抜数)は65万回であった。When this material was welded at 710°C, the welding speed without blowholes was 30C11/min, and the punching performance with a 205mφ steel die (number of punches up to a burr height of 50m) was 650,000 times. there were.
比較例4
比較材として、実施例2と同一材種の鋼板に処理液E(
粘度8200cp )を実施例2と同一条件で塗布した
ところ、得られた皮膜の目付量は6.3 g/ポであり
、表面粗度Raは0.81μmであった。Comparative Example 4 As a comparative material, treatment liquid E (
When a film with a viscosity of 8200 cp) was applied under the same conditions as in Example 2, the coating weight of the obtained film was 6.3 g/po, and the surface roughness Ra was 0.81 μm.
この材料をTIG溶接による、ブローホールの発生しな
い溶接速度は120cm/分であり、20■φのスチー
ルダイスでの打抜性(カエリ高さ50μmまでの打抜数
)は70%回であり、良好な結果を得た。When this material is TIG welded, the welding speed without blowholes is 120 cm/min, and the punching performance (number of punches up to a burr height of 50 μm) with a 20 φ steel die is 70%. Good results were obtained.
しかし、塗布作業時にロール周辺に処理液が付着し、ロ
ールの清掃に長時間を要し、作業性が非常に悪かった。However, during the coating operation, the processing liquid adhered to the periphery of the roll, and it took a long time to clean the roll, resulting in very poor workability.
水溶性アルキッド/メラミン系樹脂
(混合比 70 : 30) (不揮発分50%)
表 1
(ml)JIS第2法
(傘2)屈曲して皮膜のmしない直径
(4)塩水噴霧試験7時間後
(祠)TIG溶接、加圧100kg/ca 120A
でプローホールの発生しない最大溶接速度
(心加閤φスチールダイス、クリアランス6%でカエリ
高さ団μmまでの打抜数
(s6)塗布ロールの清掃に要する時間〔処理液D〕
水分散エマルジョン樹脂
アクリル−酢酸ビニル系
(混合比 80 j 20) (不揮発分50%)
〔処理液E]
水溶性エポキシ/メラミン系樹脂
(混合比 70:30) (不揮発分50%)なお
、他の皮膜緒特性は表1に示す。Water-soluble alkyd/melamine resin (mixing ratio 70:30) (non-volatile content 50%)
Table 1 (ml) JIS Method 2 (Umbrella 2) Diameter of the film when bent (4) After 7 hours of salt spray test (shrine) TIG welding, pressure 100 kg/ca 120 A
Maximum welding speed at which no plow holes occur (Shinkako φ steel die, number of punches up to a burr height of μm with a clearance of 6% (s6)) Time required to clean the application roll [Treatment liquid D] Water-dispersed emulsion resin Acrylic-vinyl acetate type (mixing ratio 80 j 20) (non-volatile content 50%)
[Treatment liquid E] Water-soluble epoxy/melamine resin (mixing ratio 70:30) (non-volatile content 50%) Other film characteristics are shown in Table 1.
〈発明の効果〉
かくして、本発明によれば、電磁鋼板の表面に絶縁皮膜
を形成する際に、粘度が300〜5000cpの分散系
処理後を用いて、塗布方法にグラビアロールを用いたピ
ックアップロールを用いナチュラルリバース方式を採用
することに゛より表面粗さがRaで0.5〜1.5μm
の絶縁皮膜が得られ、従来相反する性質とされていた打
抜性と溶接性を同時に満足する絶縁皮膜を得ることがで
きた。<Effects of the Invention> Thus, according to the present invention, when forming an insulating film on the surface of an electrical steel sheet, a pick-up roll using a gravure roll for the coating method is used after dispersion treatment with a viscosity of 300 to 5000 cp. By adopting the natural reverse method using
It was possible to obtain an insulating film that simultaneously satisfies punchability and weldability, which were conventionally considered to be contradictory properties.
特許出願人 川崎製鉄株式会社Patent applicant: Kawasaki Steel Corporation
Claims (1)
調整した、リン酸塩系、クロム酸塩系、および重クロム
酸塩系の一種以上の処理液と有機樹脂とを混合した処理
液、あるいは水溶性樹脂、あるいはエマルジョン樹脂の
いずれかの皮膜処理液をグラビアロールをピックアップ
ロールとしたナチュラル・リバース方式で塗布し、次い
で焼付け処理を行ない表面粗さをRaで0.5〜1.5
μmとすることを特徴とする打抜性および溶接性の優れ
た電磁鋼板の絶縁皮膜の形成方法。A treatment liquid containing an organic resin and one or more of phosphate-based, chromate-based, and dichromate-based treatment liquids, each with a viscosity adjusted to 300 to 5000 cp, or an aqueous solution is applied to the surface of the electrical steel sheet. A film treatment solution of either a synthetic resin or an emulsion resin is applied using a natural reverse method using a gravure roll as a pick-up roll, and then baked to achieve a surface roughness of Ra of 0.5 to 1.5.
A method for forming an insulating film on an electrical steel sheet with excellent punchability and weldability, characterized by having a thickness of .mu.m.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27040887A JPH01116085A (en) | 1987-10-28 | 1987-10-28 | Formation of insulating coat having superior suitability to blanking and welding on electrical steel sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27040887A JPH01116085A (en) | 1987-10-28 | 1987-10-28 | Formation of insulating coat having superior suitability to blanking and welding on electrical steel sheet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01116085A true JPH01116085A (en) | 1989-05-09 |
Family
ID=17485846
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27040887A Pending JPH01116085A (en) | 1987-10-28 | 1987-10-28 | Formation of insulating coat having superior suitability to blanking and welding on electrical steel sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01116085A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996034995A1 (en) * | 1995-05-06 | 1996-11-07 | Henkel Kommanditgesellschaft Auf Aktien | Chromium- and fluoride-free treatment of metallic surfaces |
JP2003526727A (en) * | 2000-03-16 | 2003-09-09 | ポーハング アイアン アンド スティール シーオー.,エルティディ. | Coating composition for forming insulating film, non-oriented electrical steel sheet coated with the coating composition, and method for forming insulating film on the steel sheet |
WO2012042865A1 (en) * | 2010-09-30 | 2012-04-05 | Jfeスチール株式会社 | Oriented electromagnetic steel plate |
-
1987
- 1987-10-28 JP JP27040887A patent/JPH01116085A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996034995A1 (en) * | 1995-05-06 | 1996-11-07 | Henkel Kommanditgesellschaft Auf Aktien | Chromium- and fluoride-free treatment of metallic surfaces |
JP2003526727A (en) * | 2000-03-16 | 2003-09-09 | ポーハング アイアン アンド スティール シーオー.,エルティディ. | Coating composition for forming insulating film, non-oriented electrical steel sheet coated with the coating composition, and method for forming insulating film on the steel sheet |
WO2012042865A1 (en) * | 2010-09-30 | 2012-04-05 | Jfeスチール株式会社 | Oriented electromagnetic steel plate |
JP2012077347A (en) * | 2010-09-30 | 2012-04-19 | Jfe Steel Corp | Oriented electromagnetic steel plate |
CN103140604A (en) * | 2010-09-30 | 2013-06-05 | 杰富意钢铁株式会社 | Grain oriented electrical steel sheet |
US10020103B2 (en) | 2010-09-30 | 2018-07-10 | Jfe Steel Corporation | Grain oriented electrical steel sheet |
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