JPH0364595A - Coating blade and its production - Google Patents
Coating blade and its productionInfo
- Publication number
- JPH0364595A JPH0364595A JP19959789A JP19959789A JPH0364595A JP H0364595 A JPH0364595 A JP H0364595A JP 19959789 A JP19959789 A JP 19959789A JP 19959789 A JP19959789 A JP 19959789A JP H0364595 A JPH0364595 A JP H0364595A
- Authority
- JP
- Japan
- Prior art keywords
- coating
- chromium
- blade
- coated
- nickel
- 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.)
- Granted
Links
- 238000000576 coating method Methods 0.000 title claims abstract description 133
- 239000011248 coating agent Substances 0.000 title claims abstract description 126
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract description 108
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 96
- 239000011651 chromium Substances 0.000 claims abstract description 96
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 45
- 239000010959 steel Substances 0.000 claims abstract description 45
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 34
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 claims abstract description 32
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 24
- 238000009713 electroplating Methods 0.000 claims abstract description 21
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 20
- 239000001257 hydrogen Substances 0.000 claims abstract description 20
- 229910052751 metal Inorganic materials 0.000 claims abstract description 17
- 239000002184 metal Substances 0.000 claims abstract description 17
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 17
- 239000000463 material Substances 0.000 claims description 42
- 238000007747 plating Methods 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 21
- 229910001096 P alloy Inorganic materials 0.000 claims description 13
- OFNHPGDEEMZPFG-UHFFFAOYSA-N phosphanylidynenickel Chemical compound [P].[Ni] OFNHPGDEEMZPFG-UHFFFAOYSA-N 0.000 claims description 13
- 238000005498 polishing Methods 0.000 claims description 12
- 238000010521 absorption reaction Methods 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 9
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 8
- 239000004327 boric acid Substances 0.000 claims description 8
- 238000005260 corrosion Methods 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 7
- 239000010949 copper Substances 0.000 claims description 7
- 229910052802 copper Inorganic materials 0.000 claims description 7
- -1 alkyl sulfonic acid Chemical compound 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 229910000521 B alloy Inorganic materials 0.000 claims description 4
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 claims description 4
- 238000001556 precipitation Methods 0.000 claims description 4
- QDWJUBJKEHXSMT-UHFFFAOYSA-N boranylidynenickel Chemical compound [Ni]#B QDWJUBJKEHXSMT-UHFFFAOYSA-N 0.000 claims description 3
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 238000003860 storage Methods 0.000 claims description 2
- 230000000694 effects Effects 0.000 abstract description 7
- 238000007639 printing Methods 0.000 abstract description 4
- 239000011247 coating layer Substances 0.000 abstract 1
- 230000008021 deposition Effects 0.000 abstract 1
- 239000010410 layer Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 24
- 238000000137 annealing Methods 0.000 description 15
- 230000003746 surface roughness Effects 0.000 description 10
- 239000003973 paint Substances 0.000 description 8
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 5
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 description 4
- 229910010293 ceramic material Inorganic materials 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 238000007751 thermal spraying Methods 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- 235000014692 zinc oxide Nutrition 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- GVEHJMMRQRRJPM-UHFFFAOYSA-N chromium(2+);methanidylidynechromium Chemical compound [Cr+2].[Cr]#[C-].[Cr]#[C-] GVEHJMMRQRRJPM-UHFFFAOYSA-N 0.000 description 2
- PYRZPBDTPRQYKG-UHFFFAOYSA-N cyclopentene-1-carboxylic acid Chemical compound OC(=O)C1=CCCC1 PYRZPBDTPRQYKG-UHFFFAOYSA-N 0.000 description 2
- 238000004070 electrodeposition Methods 0.000 description 2
- 238000007772 electroless plating Methods 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
- 239000001095 magnesium carbonate Substances 0.000 description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 2
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 2
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 2
- 238000007517 polishing process Methods 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 229910010271 silicon carbide Inorganic materials 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 229910003470 tongbaite Inorganic materials 0.000 description 2
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241001391944 Commicarpus scandens Species 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 241001422033 Thestylus Species 0.000 description 1
- 229910001315 Tool steel Inorganic materials 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical class C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- KERTUBUCQCSNJU-UHFFFAOYSA-L nickel(2+);disulfamate Chemical compound [Ni+2].NS([O-])(=O)=O.NS([O-])(=O)=O KERTUBUCQCSNJU-UHFFFAOYSA-L 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- XTUPUYCJWKHGSW-UHFFFAOYSA-L zinc;2-carboxy-4,6-bis(1-phenylethyl)phenolate Chemical compound [Zn+2].C=1C(C(C)C=2C=CC=CC=2)=C(O)C(C([O-])=O)=CC=1C(C)C1=CC=CC=C1.C=1C(C(C)C=2C=CC=CC=2)=C(O)C(C([O-])=O)=CC=1C(C)C1=CC=CC=C1 XTUPUYCJWKHGSW-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05C—APPARATUS FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05C11/00—Component parts, details or accessories not specifically provided for in groups B05C1/00 - B05C9/00
- B05C11/02—Apparatus for spreading or distributing liquids or other fluent materials already applied to a surface ; Controlling means therefor; Control of the thickness of a coating by spreading or distributing liquids or other fluent materials already applied to the coated surface
- B05C11/04—Apparatus for spreading or distributing liquids or other fluent materials already applied to a surface ; Controlling means therefor; Control of the thickness of a coating by spreading or distributing liquids or other fluent materials already applied to the coated surface with blades
- B05C11/045—Apparatus for spreading or distributing liquids or other fluent materials already applied to a surface ; Controlling means therefor; Control of the thickness of a coating by spreading or distributing liquids or other fluent materials already applied to the coated surface with blades characterised by the blades themselves
Landscapes
- Coating Apparatus (AREA)
- Electroplating Methods And Accessories (AREA)
- Paper (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は塗工用ブレードに関するものであり、印刷用塗
被紙、感圧複写紙、或いは感熱記録紙等の塗被紙製造工
程において原紙に顔料及び接着剤を主成分とする水性塗
料などを塗布するいわゆる塗工工程で利用されるもので
ある。Detailed Description of the Invention [Industrial Application Field] The present invention relates to a coating blade, which is used to coat base paper in the manufacturing process of coated paper such as printing coated paper, pressure-sensitive copying paper, or heat-sensitive recording paper. It is used in the so-called coating process, in which water-based paints containing pigments and adhesives as main components are applied to surfaces.
[従来の技術]
従来、原紙への塗工に利用される塗工用ブレード(コー
ターブレード)は、厚みが約0.2〜0.8mmで板幅
が約50〜150mm、長さが約1500〜7000m
mに及ぶ可撓性を有する鋼材、例えばJ I 5−G−
4401に制定される炭素工具鋼鋼材(SK材)や5U
S410などで構成されている。[Prior Art] Conventionally, a coating blade (coater blade) used for coating base paper has a thickness of about 0.2 to 0.8 mm, a plate width of about 50 to 150 mm, and a length of about 150 mm. ~7000m
Steel materials having flexibility up to m, such as J I 5-G-
Carbon tool steel (SK material) and 5U specified in 4401
It is composed of S410 and the like.
塗工用ブレードは塗布する塗料の塗布量に応じてブレー
ド先端を利用するヘヘルブレードと、ブレードの側面を
利用するベントブレードとに大別されるが、いずれにし
ても原紙とこれに塗布される塗料とで連続的に擦すられ
ているために、ブレード鋼材が比較的短時間て摩耗によ
る損傷を受けているのが実状である。Coating blades are roughly divided into two types, depending on the amount of paint to be applied: heher blades that use the tip of the blade, and bent blades that use the side of the blade. The reality is that the blade steel is damaged by wear in a relatively short period of time due to continuous rubbing.
塗工用ブレードの摩耗による損傷を極力防止し、耐久性
を増す試みとして、例えば、特開昭5988995号公
報が挙げられる。これは、ブレード用の鋼材に対してセ
ラミック材料、特にアルミナ、アルミナ−チタニア、酸
化クロムなどを溶射法によって被覆したものである。For example, Japanese Patent Application Laid-Open No. 5988995 is an attempt to prevent damage caused by abrasion of coating blades as much as possible and increase durability. This is a blade steel material coated with a ceramic material, particularly alumina, alumina-titania, chromium oxide, etc., by a thermal spraying method.
ところが、上記公報によるブレードは、従来からのブレ
ードと比べると耐摩耗性が改良されてはいるが、原紙と
の接触面近傍が全てセラミックで被覆されていないため
に発錆したり、セラミック材特有の脆さと多孔性のため
に欠落したり多孔性に起因する接触面上てのボイドの発
生があって、必ずしも満足できるものではない。さらに
、セラミック材料を溶射するためには、セラミック材料
が高融点であるところから少なくとも数千度〜数万度の
プラズマ炎もしくはカス火炎で材料を溶融・吹き付けし
なければならないといった制約があった。そのため、ブ
レード材の変形をもたらすなどの問題があるだ(うてな
く、ブレードとしての接触部の平坦性や平滑性を保持す
るために溶射後の研摩を必須とするなどの難点があった
。However, although the blade according to the above-mentioned publication has improved wear resistance compared to conventional blades, the area near the contact surface with the base paper is not entirely coated with ceramic, so it may rust or cause problems peculiar to ceramic materials. This is not always satisfactory because of the brittleness and porosity of the material, which results in chipping and the formation of voids on the contact surface due to the porosity. Furthermore, in order to thermally spray ceramic materials, there is a restriction that the material must be melted and sprayed using a plasma flame or dregs flame at a temperature of at least several thousand to tens of thousands of degrees, since ceramic materials have a high melting point. As a result, there are problems such as deformation of the blade material (not to mention problems such as the need for polishing after thermal spraying in order to maintain the flatness and smoothness of the contact area of the blade).
[発明が解決しようとする課題]
本発明は被覆の脆さによる欠落や被覆の不完全さによる
発錆を防止できる塗工用ブレードを提供すると共に、併
せて変形のない塗工用ブレードを経済的に製造する方法
を提供することを目的とするものである。[Problems to be Solved by the Invention] The present invention provides a coating blade that can prevent rusting due to breakage due to brittle coating and incomplete coating, and also provides an economical coating blade that does not deform. The purpose of this invention is to provide a method for manufacturing the same.
[課題を解決するための手段]
本発明にあっては、」1記の課題を解決するために、可
撓性の鋼からなる塗工用ブレードにおいて、塗工用原紙
との接触部近傍に、水素吸蔵を妨げるクロム以外の金属
を被覆し、該被覆上にクロムを5μm以上て且つ鋼材の
厚みよりも薄く被覆したことを特徴とするものである。[Means for Solving the Problems] In the present invention, in order to solve the problem described in item 1, in the coating blade made of flexible steel, a coating blade is provided near the contact portion with the base paper for coating. It is characterized in that it is coated with a metal other than chromium that prevents hydrogen absorption, and that chromium is coated on the coating to a thickness of 5 μm or more and thinner than the thickness of the steel material.
別の手段として、鋼に対する防食性を有し水素吸蔵を妨
げるクロム以外の金属をブレードの全面に被覆して、該
被覆の塗工用原紙との接触部近傍に、クロムを5μIn
以上で且つ鋼材の厚みよりも薄く被覆しても良い。Another method is to coat the entire surface of the blade with a metal other than chromium, which has anti-corrosion properties against steel and prevents hydrogen absorption, and injects 5μIn of chromium into the vicinity of the contact area of the coating with the base paper for coating.
The coating may be made thinner than the thickness of the steel material.
また、クロム以外の金属を被覆する代わりに、クロム被
覆を施した後、1.10℃〜145℃でアニールしても
良い。さらに、クロム被覆は電気めっき法により形成し
、電気めっき液の組成は無水クロム酸が100〜,10
0g/N、硫酸が無水り177ノ\酸濃度の1/70〜
1/120量で、液温か35〜65°Cでクロム析出に
よる応力が±1.5 K g/ mm2以下とすること
を特徴とするものである。Further, instead of coating with a metal other than chromium, it may be coated with chromium and then annealed at 1.10°C to 145°C. Furthermore, the chromium coating is formed by electroplating, and the composition of the electroplating solution is chromic anhydride ranging from 100 to 10.
0g/N, sulfuric acid is 1/70 of the anhydrous 177n acid concentration
It is characterized in that the amount is 1/120 and the stress due to chromium precipitation is less than ±1.5 K g/mm2 at a liquid temperature of 35 to 65°C.
[作用]
本発明者らは、上記の課題を解決する/こめに、被覆材
料の選定、摩耗試験、被覆の欠けの原因解析、研摩工程
の省略、耐食性の付与等について詳細な検討を行った。[Function] In order to solve the above problems, the present inventors conducted detailed studies on the selection of coating materials, wear tests, analysis of the causes of coating chipping, omission of the polishing process, provision of corrosion resistance, etc. .
喪艷辻牝へl攬
まず、本発明者らはブレード鋼材の被覆材料を決定する
べく、各種の被覆の摩耗減量をテーバー式摩耗試験機に
より測定することで適切な被覆を検討した。その結果を
第1表に示す。表中、摩耗減量の単位は〔mFi/ 1
000rev、)である。また、第1表には各被覆硬度
[11V )の測定値を併記した。Firstly, in order to determine the coating material for the blade steel, the present inventors investigated appropriate coatings by measuring the wear loss of various coatings using a Taber type abrasion tester. The results are shown in Table 1. In the table, the unit of wear loss is [mFi/1
000rev, ). Table 1 also lists the measured values of each coating hardness [11V].
第1表
第1表において、被覆形成後の処置Aは研摩のままとし
、処置Bは研摩f!t200℃で1時間アニールした。Table 1 In Table 1, treatment A after coating formation is left as polishing, and treatment B is polishing f! Annealing was performed at t200°C for 1 hour.
被覆と擦り合わせる相手材はシリコンカーバイト(H−
1,0)とした。シリコンカーバイトには荷重IKgを
付加しである。S K −5の化学組成は、C:0.8
0〜0.90、Si:<0.35、Mn:<0.50.
P:<0.03、S:<0.03である。アルミナ−チ
タニアの組成は、A12033%Ti○2とした。被覆
の厚みはいずれも0.15mmである。The material to be rubbed against the coating is silicon carbide (H-
1,0). A load of Ikg is added to silicon carbide. The chemical composition of S K-5 is C: 0.8
0-0.90, Si:<0.35, Mn:<0.50.
P:<0.03, S:<0.03. The composition of alumina-titania was A12033%Ti○2. The thickness of each coating is 0.15 mm.
第1表から明らかなように、比較した被覆の中では、ク
ロムめっきの摩耗特性が最も良好で、5K−5に対して
は約10倍、アルミナーヂタニアに対しては約4倍の耐
摩耗性を示し、ブレードへの被覆に適したものであるこ
とが判明した。As is clear from Table 1, among the compared coatings, chrome plating has the best wear properties, about 10 times as resistant to 5K-5 and about 4 times as resistant to alumina ditania. It was found to be abrasive and suitable for coating blades.
艷1絞1
次に、上記被覆を実際にブレードに適用して、テストコ
ーターによる摩耗試験を試みた。S K −5#I材か
ら第4図に示すように幅u+−55mm、長さN=50
0mm、厚みd=0.5+nmのブレードを作製した。1 draw 1 Next, the above coating was actually applied to a blade, and an abrasion test using a test coater was attempted. Width u+-55mm, length N=50 as shown in Figure 4 from S K-5#I material
A blade having a thickness of 0 mm and a thickness of d=0.5+nm was produced.
図中、d、−0、1man、θ−30°である。In the figure, d is −0, 1 man, and θ−30°.
このブレードに対して、溶射法によりアルミナ−チタニ
ア、クロムカーバイト、めっき法によりクロム、ニッケ
ル−リン合金の被覆を形成した。被覆範囲は第5図のよ
うに設定し、被覆幅l111−10+nmとした。被覆
の厚みは100 μm(0、1mm)を目標厚みとした
が、ニッケル−リン合金を除いて、いずれもブレード鋼
に変形(曲がり)を生した。溶射法による被覆、つまり
アルミナ−チタニアについては変形が僅かであったのて
、そのまま利用することにしたが、クロムカーバイトに
ついては変形が著しいので、試験を中断した。This blade was coated with alumina-titania and chromium carbide by thermal spraying, and chromium and nickel-phosphorus alloy by plating. The coverage range was set as shown in FIG. 5, and the coverage width was 111-10+ nm. Although the target thickness of the coating was 100 μm (0.1 mm), deformation (bending) occurred in the blade steel in all cases except for the nickel-phosphorus alloy. The thermal spray coating, that is, alumina-titania, showed only slight deformation, so it was decided to use it as is, but the chromium carbide coating had significant deformation, so the test was discontinued.
また、めっき法によるクロム被覆については、種々検討
した結果、クロムめっきを析出させることによって生ず
るクロムめっきの内部応力が引張側の応力にしろ圧縮側
の応力にしろ、被覆厚みが5μmを越える場合において
1.5Kg7mm2を越える場合に変形をもたらすこと
が判明した。そして、応力を上記範囲内とするには、ク
ロムめっき液中の成分である無水クロム酸を1. OO
〜400g/l、好ましくは250〜350g#とじ、
硫酸を無水クロム酸の]/70〜1/120量、好まし
くは1770〜1/90量とした組成て液温が35〜6
5℃、好ましくは40〜48℃とした条件で電流密度を
選ぶことにより殆ど変形のない状態でクロムを被覆でき
ることを発見した。In addition, as a result of various studies regarding chromium coating by plating, we have found that when the coating thickness exceeds 5 μm, whether the internal stress of the chromium plating caused by depositing the chromium plating is tensile stress or compressive stress, It was found that deformation occurs when the weight exceeds 1.5 kg and 7 mm2. In order to keep the stress within the above range, chromic anhydride, which is a component in the chromium plating solution, should be added to OO
~400g/l, preferably 250-350g# binding,
The composition contains sulfuric acid in an amount of 1/70 to 1/120 of chromic anhydride, preferably 1/770 to 1/90, and the liquid temperature is 35 to 6.
It has been discovered that by selecting the current density at 5°C, preferably 40 to 48°C, chromium can be coated with almost no deformation.
ところで、塗被紙を製造する塗工工程で利用される塗料
は、印刷用塗被紙の場合は、水、分散剤、接着剤、顔料
及び助剤などから成り、感圧複写紙の場合は、顕色剤、
接着剤、マイクロカプセル等から戒り、感熱記録紙の場
合は顕色剤、染料、接着剤等から戒り立っているが、ブ
レードの摩耗は原紙と連続的に接触し、且つ擦ずれるだ
けでなく、塗料に含まれる成分、特に顔料に使用される
無機質材料によりブレード鋼の摩耗が促進され、比較的
短時間での交換を余儀なくされている。そして、顔料と
して利用される無機質成分としては、フレ、焼成カオリ
ン、炭酸カルシウム、タルク、シリカサチン白、チタン
白、水酸化アルミニウム、活性白土、微粒シリカ、酸化
亜鉛、有機顔料などが代表的であるが、これらを総括す
ると、カルシウムの炭酸塩や硫酸塩、マグネシウムの炭
酸塩、チタンの酸化物、バリウムの硫酸塩、アルミニウ
ムの水和物、亜鉛華、カルシウム・マグネシウム炭酸塩
、ケイ酸及びそのケイ酸塩などであり、印刷用塗被紙、
感圧複写紙、感熱記録紙、インクジェット記録紙等の塗
被紙に要求される性状に応じて、これらを適宜選択し、
混合して利用しているのが実状である。By the way, the paint used in the coating process for manufacturing coated paper consists of water, dispersant, adhesive, pigment, auxiliary agent, etc. in the case of coated paper for printing, and in the case of pressure-sensitive copying paper. , developer,
In the case of heat-sensitive recording paper, there are precautions against adhesives, microcapsules, etc., and in the case of thermal recording paper, there are precautions against color developers, dyes, adhesives, etc., but the wear of the blade is caused by continuous contact with the base paper and only by rubbing However, the components contained in the paint, especially the inorganic materials used in the pigments, accelerate the wear of the blade steel, making it necessary to replace it within a relatively short period of time. Typical inorganic components used as pigments include fluoride, calcined kaolin, calcium carbonate, talc, silica satin white, titanium white, aluminum hydroxide, activated clay, fine silica, zinc oxide, and organic pigments. To summarize these, calcium carbonate and sulfate, magnesium carbonate, titanium oxide, barium sulfate, aluminum hydrate, zinc white, calcium/magnesium carbonate, silicic acid and its silicic acid. Salt, etc., coated paper for printing,
These are selected as appropriate depending on the properties required for coated paper such as pressure-sensitive copying paper, thermal recording paper, inkjet recording paper, etc.
The reality is that they are used in combination.
テストコーターでは、塗料の配合を次のように行い、水
により固形分濃度を60%としたものを試験に利用した
。In the test coater, the paint was formulated as follows, and the solid content concentration was adjusted to 60% with water and used in the test.
カオリン 80重量部炭酸カルシウ
ム 20重量部ピロリン酸ナトリウム
0.1重量部スチレン・フ゛タシ゛エンラテックス
12重i部澱粉
5重量部また、テストコーターの運転条
件は次のように設定し、被覆されたブレードの原紙との
接触面の変化を逐次調査した。Kaolin 80 parts by weight Calcium carbonate 20 parts by weight Sodium pyrophosphate
0.1 parts by weight styrene/phthalene latex 12 parts by weight starch
Further, the operating conditions of the test coater were set as follows, and changes in the contact surface of the coated blade with the base paper were successively investigated.
速度: 1. OOOm/minブレード線
圧+ 0.8Kg/cn+原紙 60g
/m2
塗被量 ]、Og/m2
ブレードのベベル面の被覆後の表面粗さは第2表の通り
であり、程度の差はあれ、元のブレード鋼よりも粗化さ
れている。そこて、被覆を設けない5K−5材を除いて
全て0.6〜0.8 μRmaxの表面粗さに研摩して
試験に供した。運転時間は2.0時間としたが、0.5
時間毎に摩耗量を調査し、結果を第2表に示した。また
、2時間運転後のベベル面の表面粗さを併記した。表面
粗さの単位は〔μRmax)である。Speed: 1. OOOm/min blade linear pressure + 0.8Kg/cn + base paper 60g
/m2 Coating amount], Og/m2 The surface roughness of the beveled surface of the blade after coating is as shown in Table 2, and although there are differences in degree, it is rougher than the original blade steel. Therefore, except for the 5K-5 material which was not provided with a coating, all the materials were polished to a surface roughness of 0.6 to 0.8 μRmax and subjected to the test. The driving time was 2.0 hours, but 0.5
The amount of wear was investigated every hour, and the results are shown in Table 2. In addition, the surface roughness of the beveled surface after 2 hours of operation is also shown. The unit of surface roughness is [μRmax].
第2表
第2表において、ブレード■は5K−5プレー11
ド、ブレード■はアルミナ−チタニア被覆を施した5K
−5ブレード、ブレード■はクロムめっき被覆を施した
5K−5ブレード、ブレード■はニッケル−リン合金被
覆を施した5K−5ブレードである。摩耗量のは0.5
時間後、摩耗量■は1.0時間後、摩耗量■は1.5時
間後、摩耗量■は20時間後の測定値である。また、表
には記載していないが、ブレード■とブレード■では、
試験後、ブレードの刃先の所々に被覆の欠けが見られた
。Table 2 In Table 2, blade ■ is 5K-5 play 11 de, blade ■ is 5K with alumina-titania coating.
-5 blade, blade (2) is a 5K-5 blade coated with chrome plating, and blade (2) is a 5K-5 blade coated with nickel-phosphorous alloy. The amount of wear is 0.5
The wear amount (■) was measured after 1.0 hours, the wear amount (■) was measured after 1.5 hours, and the wear amount (■) was measured after 20 hours. Also, although not listed in the table, Blade ■ and Blade ■
After the test, the coating was found to be chipped in some places on the cutting edge of the blade.
第2表から、クロムめっき被覆を施したブレード■は、
刃先に部分的な欠けが見られるものの、SK −5鋼材
と比べると約4倍の耐久性を示し、被覆選定試験の結果
が裏付けられた。From Table 2, the blade ■ with chrome plating coating is:
Although some chipping was observed on the cutting edge, the durability was approximately four times greater than that of SK-5 steel, confirming the results of the coating selection test.
のハ(の原
上述のように、クロム被覆を施したブレードは局部的な
がら刃先に欠けが見られ、均一な塗工という観点からは
欠けの発生した時点がブレードとしての寿命ということ
になって、クロムの耐摩耗性を発揮できない場合も起こ
り得る。そこで、被覆の欠けの発生原因を解明するため
に種々の検討2
を加えた。(Original) As mentioned above, chrome-coated blades show chipping at the cutting edge, albeit locally, and from the perspective of uniform coating, the point at which chipping occurs is the end of the blade's lifespan. There may also be cases where the wear resistance of chromium cannot be demonstrated.Therefore, various studies were conducted to clarify the cause of coating chipping.
本発明者らは、長さ100mm、幅10mm、厚み0.
5mmの5K−5材を用意し、これにクロムを5μm、
TOμm、50μm、100μm、300 μm全面に
被覆したものと、予めニッケルを3μIl+。The inventors have a length of 100 mm, a width of 10 mm, and a thickness of 0.
Prepare 5mm 5K-5 material, add 5μm of chromium to it,
TOμm, 50μm, 100μm, 300μm whole surface coating and 3μIl+ of nickel in advance.
5μm、50μm全面に被覆した後、クロムを3μm0
.5μm、100μm被覆したものと、無電解ニッケル
めっきによりニッケル−リン合金を予め5μIn被覆し
てクロムを100μm被覆したものと、シアン化銅浴を
利用して銅を5μm被覆し、次いでクロムを100μm
被覆したものなどを用意し、これらの被覆を施したこと
により、素材が欠は易くなっているのか否かを確認した
。その結果を第3表に示す。具体的には素材を90度折
り曲げて脆化の程度を確認する方法を採った。After coating the entire surface with 5 μm and 50 μm, 3 μm of chromium was applied.
.. One coated with 5μm and 100μm of nickel, one coated with 5μIn of nickel-phosphorous alloy by electroless nickel plating and coated with 100μm of chromium, and the other coated with 5μm of copper using a copper cyanide bath and then coated with 100μm of chromium.
We prepared coated materials and confirmed whether the coating made the materials more prone to chipping. The results are shown in Table 3. Specifically, a method was used to check the degree of embrittlement by bending the material 90 degrees.
(以下余白)
第3表
表中、○は折り曲げても破損しない、△は折り曲げると
破損する場合と破損しない場合がある、×は折り曲げる
と完全に破損することを示す。第3表によれば、クロム
だけを被覆した5K−5材において、被覆の厚みが5μ
mを越えると、破損しやすくなっていることが認められ
、これがテストコーターでのブレード刃先の部分的欠け
の原因と考えられる。(Margin below) In Table 3, ◯ indicates that the product will not be damaged even if it is bent, △ indicates that it may or may not be damaged when it is bent, and × indicates that it will be completely damaged when it is bent. According to Table 3, for 5K-5 material coated only with chromium, the thickness of the coating is 5μ.
It was found that when the thickness exceeds m, it becomes easy to break, and this is thought to be the cause of partial chipping of the blade edge in the test coater.
本発明者らはクロムとS K −5材との中間層にニッ
ケルやニッケル−リン合金、銅などを被覆しておくと、
中間層の厚みが僅か5μmから素材の脆化を防止できる
ことを発見した。また、テストコーターで利用したクロ
ム被覆ブレードのクロム被覆部と未被覆部とから長さ1
00mmの折り曲げ試験片を切り出し、同じように折り
曲げて見るとクロム被覆部にのみ脆化が見られた。した
がって、脱化はクロムを被覆することによりクロム被覆
部にのみ生ずる現象と考えられ、これはクロムめっき時
に発生する水素ガス吸蔵の結果としての水素脆性である
と推定された。そして、脆化が水素脆性であればクロム
被覆後、アニールすると脱水素され、脆性除去できるは
ずで、事実、水素脆性除去温度として一般的な150〜
250℃の範囲で5
アニールすると、脆化そのものは除去することが可能で
あった。ところが、上記の一般的なアニール温度では弊
害としてブレード鋼材として必要なバネ性が変化するな
どの問題を呈した。そこで、バネ性(可撓性)を変化さ
せずに脆化を除去できるか否かを詳細に検討したところ
、1.10〜145°C1望ましくは130〜145℃
でアニールすると、可視性の変化なしに脆性を除去でき
ることを発見した。The present inventors discovered that by coating the intermediate layer between chromium and S K-5 material with nickel, nickel-phosphorus alloy, copper, etc.
It has been discovered that embrittlement of the material can be prevented when the thickness of the intermediate layer is only 5 μm. Also, the length 1 from the chrome coated part and uncoated part of the chrome coated blade used in the test coater.
When a 00 mm bending test piece was cut out and bent in the same manner, embrittlement was observed only in the chromium coated portion. Therefore, deoxidization was considered to be a phenomenon that occurs only in the chromium-coated area due to chromium coating, and this was presumed to be hydrogen embrittlement as a result of hydrogen gas absorption that occurs during chromium plating. If the embrittlement is hydrogen embrittlement, it should be possible to dehydrogenate and remove the embrittlement by annealing after coating with chromium.
It was possible to remove the embrittlement itself by annealing in the range of 250°C for 5 days. However, the above-mentioned general annealing temperature presents problems such as changes in the springiness required for the blade steel material. Therefore, we investigated in detail whether embrittlement could be removed without changing the springiness (flexibility), and found that
We found that annealing with 200°C can remove the brittleness without any change in visibility.
第1図(、)〜(d)はアニールにより脆性を除去した
ベントタイプのブレードの断面図、同図(e)、(f)
はアニールにより脆性を除去したベベルタイプのブレー
ドの断面図である。図中、1はブレード鋼材、2はクロ
ムめっき被覆である。第2図(、)、(b)はアニール
せずに中間層3の存在により脆性を除去したベントタイ
プのブレードの断面図、第2図(c)はアニールせずに
中間層3の存在により脆性を除去したベベルタイプのブ
レードの断面図である。この場合の中間層3は、ニッケ
ル、ニッケルリン合金、ニッケル−ホウ素合金、又は銅
より6
なり、その厚みは3〜50μmとする。Figures 1 (,) to (d) are cross-sectional views of bent-type blades whose brittleness has been removed by annealing, and Figures (e) and (f).
is a cross-sectional view of a bevel type blade whose brittleness has been removed by annealing. In the figure, 1 is a blade steel material, and 2 is a chrome plating coating. Figures 2(,) and (b) are cross-sectional views of a bent type blade in which brittleness has been removed by the presence of the intermediate layer 3 without annealing, and Figure 2(c) is a cross-sectional view of a bent type blade in which brittleness has been removed by the presence of the intermediate layer 3 without annealing. FIG. 3 is a cross-sectional view of a bevel type blade from which brittleness has been removed. In this case, the intermediate layer 3 is made of nickel, nickel phosphorus alloy, nickel-boron alloy, or copper, and has a thickness of 3 to 50 μm.
輯4LE糧!ど邑壓□
本発明者らは、ブレード鋼材にクロムを被覆するにあた
って、クロムめっき液の組成を選ぶと、変形のないクロ
ム被覆ブレードを得ることができるだけでなく、クロム
被覆後の研摩工程を省略できると考えた。このような目
的でクロムめっき液の組成について種々検討を加えた結
果、無水クロム酸100〜400g//!に硫酸を無水
クロム酸濃度の1/70〜1/1.20量加えた液に、
ケイフッ酸、ケイフッ酸塩(例えばケイフッ化ナトリウ
ム)、ホウ酸、ホウ酸塩(例えばホウ砂)、スルファミ
ン酸、アルキルスルホン酸などを1〜25g/lの割合
で加えると、平滑で事実上クロム被覆後の仕上げ研摩を
不要にできるだけでなく、応力による変形のないブレー
ドが得られることを発見した。4LE food! The present inventors found that when coating blade steel with chromium, by selecting the composition of the chromium plating solution, it was possible not only to obtain a chromium-coated blade without deformation, but also to omit the polishing process after coating with chromium. I thought it could be done. As a result of various studies on the composition of the chromium plating solution for this purpose, we found that the composition of the chromium plating solution was 100 to 400 g//! To a solution in which sulfuric acid was added in an amount of 1/70 to 1/1.20 of the concentration of chromic anhydride,
Addition of fluorosilicic acid, fluorosilicic acid salts (e.g. sodium fluorosilicic acid), boric acid, borates (e.g. borax), sulfamic acid, alkyl sulfonic acids, etc. at a rate of 1 to 25 g/l results in a smooth and virtually chromium-coated surface. We discovered that not only can we eliminate the need for subsequent final polishing, but we can also obtain blades that do not deform due to stress.
第4表は研摩された5K−4鋼材上に各種クロム被覆を
施したブレードの被覆完了後の表面粗さ〔μRmax)
を触針法で測定したデータ、及び被覆硬度CHV (1
00/30))、さらにスパイラルコントラクトメータ
ーにより計測した電着応力CKg/mm2:]のデータ
などを示した。Table 4 shows the surface roughness [μRmax] of blades made of polished 5K-4 steel with various chromium coatings after the coating is completed.
The data measured by the stylus method and the coating hardness CHV (1
00/30)), and data of electrodeposition stress CKg/mm2:] measured by a spiral contractometer.
第4表
第4表において、No、1のクロム液の組成は、無水ク
ロム酸300g/l、硫酸4g/L No、2のクロム
液の組成は、無水クロム酸300g/l、硫酸4g/l
、ホウ酸5g/l、No、3のクロム液の組成は無水ク
ロム酸300g/fl、硫酸2.5g/R、ケイフッ化
ナトリウム1.5g/lである。また、応力の一符号は
圧縮側応力を示す。なお、未被覆のS K −4材の表
面粗さは0.90〜○ 95μRmax、硬度は583
f−i V (100730)てあった。Table 4 In Table 4, the composition of the chromium solution No. 1 is chromic anhydride 300g/l and sulfuric acid 4g/L The composition of the chromium solution No. 2 is chromic anhydride 300g/l and sulfuric acid 4g/l
, boric acid 5 g/l, No. 3, the composition of the chromium solution is chromic anhydride 300 g/fl, sulfuric acid 2.5 g/R, and sodium silicofluoride 1.5 g/l. Moreover, one sign of stress indicates compression side stress. The surface roughness of the uncoated S K-4 material is 0.90~○95μRmax, and the hardness is 583.
fi V (100730).
第4表から明らかなように、No、1のクロム液を除い
て、ボウ酸やケイフッ化ナトリウムなどを添加すると、
元々の素材粗さよりも平滑化され、なお且つ低応力とな
っていることか分かる。また、付随効果として硬度の増
加が認められた。なお、これらのクロム被覆されたS
K −4材を90度に折り曲げてみると、No4,2.
3の各クロム液によるクロム被覆はいずれも素材から簡
単に破損することか分かった。また、アニールもしくは
ニッケル、ニッケル−リン合金、銅などを5μm以」二
車前に被覆しておくと、N o 、 2及びNo、3の
クロム液についても脱化防止に効果を発揮することを認
めた。以上のように、無水クロム酸と硫酸を含む液にケ
イフッ酸及びその塩、ホウ酸及びその塩、スルファミン
酸、アルキルスルホン酸などを適量添加すると、変形の
全く無い、しかもクロム被覆後の研摩を不要としたブレ
ードを作製できた。As is clear from Table 4, when boric acid, sodium silicofluoride, etc. are added except for No. 1 chromium solution,
It can be seen that the roughness of the material is smoother than the original roughness, and the stress is low. Additionally, an increase in hardness was observed as an accompanying effect. In addition, these chromium-coated S
When the K-4 material was bent at 90 degrees, No. 4, 2.
It was found that the chrome coatings made with each of the chromium solutions in No. 3 were easily damaged from the material. In addition, it has been found that annealing or coating nickel, nickel-phosphorus alloy, copper, etc. with a thickness of 5 μm or more in front of the vehicle is effective in preventing deoxidization of chromium solutions No. 2 and No. 3. Admitted. As mentioned above, when appropriate amounts of fluorosilicic acid and its salts, boric acid and its salts, sulfamic acid, alkylsulfonic acids, etc. are added to a solution containing chromic anhydride and sulfuric acid, there is no deformation at all, and polishing after chromium coating is possible. I was able to create a blade that was no longer needed.
9
紅慮1ノ■EL
クロム被覆ブレードは従来のクロムを被覆していないブ
レードに比べて著しく寿命延長効果が見られたが、従来
のブレードでは短寿命の故に問題とするに足らなかった
鋼材の発錆が耐久性(寿命)の延長に伴って新たな問題
を提起するに至った。9 Red Plan 1 ■ EL The chromium-coated blade had a significant life extension effect compared to conventional blades that were not coated with chromium. Rust has come to pose a new problem with the extension of durability (life).
そこで、その解決策としてクロム被覆ブレードで生ずる
素材鋼材の脆化(水素脆性)の防止に利用できるニッケ
ルやニッケル−リン合金被覆をブレードの特定部分だけ
でなく全面に被覆すればクロム未被覆部の発錆を防止で
き、同一被覆で脆化防止と発錆防止とを同時に行えるこ
とになるので、頗る経済的である。Therefore, as a solution to this problem, coating not only specific parts of the blade but also the entire blade with nickel or nickel-phosphorus alloy coating, which can be used to prevent the embrittlement (hydrogen embrittlement) of the steel material that occurs with chromium-coated blades, will remove the chromium-uncoated parts. Rust can be prevented, and the same coating can simultaneously prevent embrittlement and rust, which is extremely economical.
第3図(a)、(b)は中間層3をブレード鋼材]の全
面に被覆して、防錆と脆化防止を兼ねたベントタイプ及
びベベルタイプのブレードの断面図である。この場合の
中間層3は、ニッケル、ニッケルリン合金、ニッケル−
ホウ素合金の少なくとも1種類の金属よりなる。FIGS. 3(a) and 3(b) are cross-sectional views of bent type and bevel type blades in which the intermediate layer 3 is coated over the entire surface of the blade steel material to prevent rust and embrittlement. In this case, the intermediate layer 3 is made of nickel, nickel phosphorus alloy, nickel-
It is made of at least one metal of boron alloy.
なお、クロム被覆ブレードの水素脆化防止に有0
効な銅については、元々銅という金属の耐食性の欠如か
ら上記目的には合致しない。ニッケルやニッケル−リン
合金の被覆法としては、ニッケルは電気めっき法が、ま
た、ニッケル−リン合金の場合には電気めっき法と無電
解めっき法のいずれをも利用できるが、脆化防止のため
には無電解めっき法の方がやや優れている。さらに、耐
食性を与えるのに必要な厚みは3μIn以上てあり、こ
の厚みは脆化防止に必要な厚みにほぼ一致する。厚みを
増加させても脆化防止機能に変化を与えず耐食性を一層
改善できるが、厚くても不経済であるばかりか、肝心の
ブレードに必要なバネ性の変化を伴うので、50)tm
以下とするの力呻了ましい。また、クロム被覆範囲も塗
工用原紙との接触部方向の先端から]、5mmまでがブ
レード用鋼材のバネ性から考えて好都合で好ましくは1
0mm以下とするのが良い。Note that copper, which is effective in preventing hydrogen embrittlement of chromium-coated blades, does not meet the above objective due to the lack of corrosion resistance of copper as a metal. For coating nickel and nickel-phosphorus alloys, electroplating can be used for nickel, and both electroplating and electroless plating can be used for nickel-phosphorus alloys, but to prevent embrittlement, Electroless plating is slightly better. Further, the thickness required to provide corrosion resistance is 3 μIn or more, and this thickness almost corresponds to the thickness required to prevent embrittlement. Even if the thickness is increased, the corrosion resistance can be further improved without changing the embrittlement prevention function.
The power of doing the following is amazing. In addition, the chromium coating range is preferably 5 mm from the tip in the direction of contact with the coating base paper, as it is convenient in view of the springiness of the steel material for the blade.
It is preferable to set it to 0 mm or less.
以上の検討結果から明らかなように、可視性の鋼からな
る塗工用ブレードにおいて、塗工用原紙との接触部近傍
に、水素吸蔵を妨げるクロム以外の金属を被覆し、該被
覆上にクロムを5μm0以上でHlつ鋼材の厚みよりも
薄く被覆することにより、本来ならばクロムが脆化され
るところを、水素吸蔵を妨げるクロム以外の金属の存在
によりクロムの水素脆性が防止され、ブレードの欠けを
防止できる。また、鋼に対する防食性を有し水素吸蔵を
妨げるクロム以外の金属をブレードの全面に被覆するこ
とにより、ブレードの発錆をも同時に防止することが可
能となる。As is clear from the above study results, in a coating blade made of visible steel, a metal other than chromium that prevents hydrogen absorption is coated near the contact area with the base paper for coating, and a metal other than chromium is coated on the coating. By coating the blade with a thickness of 5 μm or more thinner than the thickness of the steel material, the hydrogen embrittlement of chromium is prevented due to the presence of metals other than chromium that prevent hydrogen absorption, which would normally cause chromium to become embrittled. Can prevent chipping. Further, by coating the entire surface of the blade with a metal other than chromium, which has anti-corrosion properties against steel and prevents hydrogen storage, it is possible to prevent rusting of the blade at the same time.
一方、ブレード鋼材とクロムとの間に上記のような中間
層を設けなくても、可視性の鋼からなる塗工用ブレード
の塗工用原紙との接触部近傍に5μm以上てあって且つ
鋼材の厚みよりも薄くクロムを被覆し、次いで110°
C〜145℃でアニルすることにより、水素脆性を除去
することができる。この際、アニール温度を上記のよう
に選ぶことにより、鋼材の可撓性を変化させることを防
止できる。On the other hand, even if the above-mentioned intermediate layer is not provided between the blade steel material and the chromium, if the coating blade made of visible steel has a coating thickness of 5 μm or more near the contact area with the coating base paper, and the steel material coated with chromium thinner than the thickness of
Hydrogen embrittlement can be removed by annealing at C to 145°C. At this time, by selecting the annealing temperature as described above, it is possible to prevent changes in the flexibility of the steel material.
また、可撓性の鋼からなる塗工用ブレードにおける少な
くとも塗工用原紙との接触部近傍に電気めっきによりク
ロムを被覆し、電気めっき液の組成は無水クロム酸が1
00〜400g/f、硫酸が無水クロム酸濃度の]/7
0〜1/120で、液温が35〜65℃でクロム析出に
よる応力が±15Kg/+nm2以下となるようなめっ
き条件とすれば、クロムめっきの電着応力を低減し、ブ
レードの変形を防止できる。In addition, at least the vicinity of the contact area with the coating base paper of the coating blade made of flexible steel is coated with chromium by electroplating, and the composition of the electroplating solution is chromic anhydride and chromium.
00-400g/f, sulfuric acid has chromic anhydride concentration]/7
0 to 1/120, the liquid temperature is 35 to 65℃, and the plating conditions are such that the stress due to chromium precipitation is ±15Kg/+nm2 or less, the electrodeposition stress of chrome plating is reduced and blade deformation is prevented. can.
さらに、電気めっき液にケイフッ酸、ケイフッ酸塩、ホ
ウ酸、ホウ酸塩、スルファミン酸、アルキルスルポン酸
のうちの少なくとも1つの化合物を加え、その添加量は
クロムめっき後の研摩を不要とする程度にクロムの平滑
性が得られる範囲とすれば、研摩工程の省略により、経
済的にブレードを作製できる。Furthermore, at least one compound selected from fluorosilicic acid, fluorosilicic acid, boric acid, borate, sulfamic acid, and alkyl sulfonic acid is added to the electroplating solution, and the amount of addition is such that polishing is not required after chromium plating. If the range is such that a certain level of chromium smoothness can be obtained, the blade can be manufactured economically by omitting the polishing step.
[実施例]
本発明者らは、5K−51材からなるベントタイプのブ
レード(幅]−00mm、長さ2220mm、厚み0.
381 mm)に対してクロム被覆範囲を先端部から1
0mmとし、4種類のクロム被覆ブレードを作製し、塗
料及びブレードコーターの操業条件3
は前記の条件と同様にして実施した。[Example] The present inventors created a bent type blade made of 5K-51 material (width) -00 mm, length 2220 mm, thickness 0.
381 mm), the chrome coating range is 1 from the tip.
0 mm, four types of chromium-coated blades were prepared, and the operating conditions of the paint and blade coater were the same as those described above.
実−旌−昨L
ブレードにクロムを40μm被覆した後、140℃で1
0時間アニールし、その後、クロム未被覆部分を防錆塗
料てコーティングした。クロム被覆に用いた電気めっき
液の組成は、無水クロム酸が300g/l、硫酸が4g
/lとした。ブレードの表面粗さは0.93〜1.0
(μRmax)、クロム被覆後では1.7〜1.8(μ
Rmay)、研摩後では0゜81〜0.85 (μRm
ax)であった。After coating the blade with 40μm of chromium, it was heated at 140℃ for 1
After annealing for 0 hours, the chromium-uncoated portions were coated with antirust paint. The composition of the electroplating solution used for chromium coating was 300g/l of chromic anhydride and 4g/l of sulfuric acid.
/l. The surface roughness of the blade is 0.93 to 1.0
(μRmax), 1.7 to 1.8 (μRmax) after chromium coating
Rmay), after polishing 0°81~0.85 (μRm
ax).
幻む組L
ブレードにニッケルを5μm全面被覆した後、クロムを
40μm被覆した。ニッケル被覆に用いた電気めっき液
の組成は、スルファミン酸ニッケルが350g//−1
塩化ニツケルが10g/f、ホウ酸が35g/βとした
。また、クロム被覆に用いた電気めっき液の組成は実施
例1と同じとした。ブレードの表面粗さは0.90〜0
.95(μRmax)、クロム被覆後では19〜22(
μRmnx)、研摩後では0.95〜1.O(μRma
x)であった。The entire blade was coated with nickel to a thickness of 5 μm, and then coated with chromium to a thickness of 40 μm. The composition of the electroplating solution used for nickel coating was 350g//-1 of nickel sulfamate.
The amount of nickel chloride was 10 g/f, and the amount of boric acid was 35 g/β. Furthermore, the composition of the electroplating solution used for chromium coating was the same as in Example 1. The surface roughness of the blade is 0.90~0
.. 95 (μRmax), 19-22 (after chromium coating)
μRmnx), 0.95 to 1. O(μRma
x).
4
塞−電電しと
ブレードにニッケルを5μmo全面被覆した後、クロム
を40材m被覆した。ニッケル被覆に用いた電気めっき
液の組成は、硫酸ニッケルが240g/l、塩化ニッケ
ルが20g/l、ホウ酸が45g/lとした。また、ク
ロム被覆に用いた電気めっき液の組成は、無水クロム酸
が300g/l、硫酸が2.5g//!、ケイフッ化す
l〜ゾリウム1.’3g/lとした。ブレードの表面粗
さは094〜0.98(μRmax)、クロム被覆後で
は0.30〜0.45(μRmax)であった。クロム
被覆後の研摩工程は省略した。4. After coating the entire surface of the blade with 5 μm of nickel, it was coated with 40 μm of chromium. The composition of the electroplating solution used for nickel coating was 240 g/l of nickel sulfate, 20 g/l of nickel chloride, and 45 g/l of boric acid. Also, the composition of the electroplating solution used for chromium coating was 300 g/l of chromic anhydride and 2.5 g/l of sulfuric acid! , silicofluoride l ~ zolium 1. '3g/l. The surface roughness of the blade was 094-0.98 (μRmax), and after chromium coating was 0.30-0.45 (μRmax). The polishing step after chromium coating was omitted.
天上IPJ4
ブレードにニッケル−リン合金を10μIn全面被覆し
た後、クロムを40μII+被覆した。ニッケル−リン
合金被覆に用いた電気めっき液の組成は、硫酸ニッケル
が30g/l、次亜リン酸ナトリウムが’J−Og/l
、クエン酸ナトリウムが1.Og#とじた。また、クロ
ム被覆に用いた電気めっき液の即成は、実施例3と同じ
とした。ブレードの表面粗さは0.9C)〜0.92(
μRmax)、クロム被覆後では0.25〜0.30(
μRmax)であった。クロム被覆後の研摩工程は省略
した。Tenjo IPJ4 The entire blade was coated with nickel-phosphorus alloy to a thickness of 10μIn, and then coated with 40μII+ of chromium. The composition of the electroplating solution used for coating the nickel-phosphorus alloy was 30 g/l of nickel sulfate and 'J-Og/l of sodium hypophosphite.
, sodium citrate is 1. Og# closed. Further, the instant preparation of the electroplating solution used for chromium coating was the same as in Example 3. The surface roughness of the blade is 0.9C) to 0.92(
μRmax), 0.25 to 0.30 (after chromium coating)
μRmax). The polishing step after chromium coating was omitted.
彪煕鮭り 未被覆の5K−5鋼材からなるブレードを用いた。Biao Hee Salmon Ri A blade made of uncoated 5K-5 steel was used.
実機操業条件において、比較用の5K−5鋼材からなる
ブレードを含め、順次使用し比較したところ、比較例1
のクロム未被覆ブレードでは、7時間操業で使用不能に
なったのに対して実施例1では28時間、実施例2では
36時間、実施例3では48時間、実施例4では52時
間の使用に耐えた。Comparative Example 1 was used and compared under actual machine operating conditions, including a blade made of 5K-5 steel material for comparison.
The chromium-uncoated blades of 2000 were unusable after 7 hours of operation, whereas in Example 1, they were unusable after 28 hours, in Example 2, 36 hours, in Example 3, 48 hours, and in Example 4, 52 hours. I endured.
大魂北」−
塗料配合として、水酸化アルミニウム65部、酸化亜鉛
20部、3,5−ジ(α−メチルベンジル)サリチル酸
亜鉛とα−メチルスチレン・スチレン共重合体との混融
物(混融比80/20)15部、ポリビニルアルコール
水溶液5部(固形分)及び水300部をボールミルで2
4時間粉砕して得た分散液に、カルボキシ変性スチレン
・ブタジェン共重合体ラテックス20部(固形分)を加
えて調製した感圧複写紙用水性塗被液を用い、ブレード
コーター条件として、スピード800+n/分、塗被固
形M5g/m2(固形分)、原紙/IOg/Io2とし
た以外は実施例1〜4と同様にして、ブレード刃の摩耗
試験をした結果、30時間使用可能であった。``Otama Kita'' - As a paint formulation, 65 parts of aluminum hydroxide, 20 parts of zinc oxide, a mixture (mixture) of zinc 3,5-di(α-methylbenzyl)salicylate and α-methylstyrene/styrene copolymer were used. 15 parts of melting ratio 80/20), 5 parts of polyvinyl alcohol aqueous solution (solid content) and 300 parts of water were mixed in a ball mill.
Using an aqueous coating liquid for pressure-sensitive copying paper prepared by adding 20 parts (solid content) of carboxy-modified styrene-butadiene copolymer latex to a dispersion obtained by grinding for 4 hours, the blade coater conditions were: speed 800+n; The blade blade was subjected to a wear test in the same manner as in Examples 1 to 4, except that the coating solids M5g/m2 (solid content) and the base paper/IOg/Io2 were used.As a result, the blade blade could be used for 30 hours.
比敦北−21
未被覆の5K−5鋼材からなるブレードを用いた以外は
実施例5と同様にして実施した。ブレードの使用可能時
間は6時間であった。Hitsukita-21 The test was carried out in the same manner as in Example 5 except that a blade made of uncoated 5K-5 steel was used. The usable time of the blade was 6 hours.
[発明の効果]
以上述べたところから明らかなように、請求項1又は2
に記載の発明によれば、クロムめっきによる耐摩耗性の
良好な被覆を備えた塗工用ブレードにおいて、クロムめ
っきの下層に水素吸蔵を防止する金属被覆を設けたこと
により水素脆性を防止でき、被覆の脆さによる欠落を防
止できるという効果がある。また、請求項3又は4に記
載の発明によれば、クロムめっきの下層の金属被覆をブ
7
レード全面に広げることにより、ブレードの発錆をも防
止できるという効果がある。[Effect of the invention] As is clear from the above description, claim 1 or 2
According to the invention described in , hydrogen embrittlement can be prevented by providing a metal coating that prevents hydrogen absorption in the lower layer of the chromium plating in a coating blade equipped with a chrome plating coating with good wear resistance. This has the effect of preventing chipping due to brittleness of the coating. Further, according to the third or fourth aspect of the present invention, by spreading the metal coating under the chromium plating over the entire surface of the blade, rusting of the blade can also be prevented.
一方、請求項5記載の発明によれば、クロムめっきの下
層に金属被覆を設けなくても、クロムめっき形成後のア
ニールにより水素脆性を防止でき、被覆の脆さによる欠
落を防止できる。しかも、アニール温度を110〜14
5℃としたことにより、ブレード鋼材の可視性が損なわ
れることを防止できるという効果がある。On the other hand, according to the invention as set forth in claim 5, hydrogen embrittlement can be prevented by annealing after forming the chromium plating, and chipping due to brittleness of the coating can be prevented even without providing a metal coating under the chromium plating. Moreover, the annealing temperature is 110-14
Setting the temperature to 5° C. has the effect of preventing the visibility of the blade steel from being impaired.
請求項6記載の発明によれば、クロム析出による応力を
小さくすることができるので、ブレードの変形を防止で
きるという効果がある。According to the invention as set forth in claim 6, the stress caused by chromium precipitation can be reduced, so there is an effect that deformation of the blade can be prevented.
請求項7記載の発明によれば、電気めっき液への添加物
によりクロムめっきの平滑性を高め、被覆後の研摩工程
を省略でき、塗工用ブレードを安価に製造できるという
効果がある。According to the seventh aspect of the invention, the smoothness of chromium plating can be improved by adding additives to the electroplating solution, the polishing step after coating can be omitted, and a coating blade can be manufactured at low cost.
第1図(a)乃至(f)、第2図(、)乃至(c)、第
3図(a) 、 (b)は本発明の塗工用ブレードのそ
れぞれ異なる断面構造を示す断面図、第4図は本発明の
塗8
工用ブレードの摩耗試験に用いたブレード鋼材の断面図
、第5図は同上のブレード鋼材に被覆を施した状態の要
部断面図である。
1はブレード鋼材、2はクロムめっき被覆、3は中間層
である。FIGS. 1(a) to (f), FIGS. 2(a) to (c), and FIGS. 3(a) and (b) are sectional views showing different sectional structures of the coating blade of the present invention, respectively, FIG. 4 is a cross-sectional view of a blade steel material used in the wear test of a coating blade of the present invention, and FIG. 5 is a cross-sectional view of a main part of the same blade steel material with a coating applied thereto. 1 is a blade steel material, 2 is a chrome plating coating, and 3 is an intermediate layer.
Claims (7)
工用原紙との接触部近傍に、水素吸蔵を妨げるクロム以
外の金属を被覆し、該被覆上にクロムを5μm以上で且
つ鋼材の厚みよりも薄く被覆したことを特徴とする塗工
用ブレード。(1) In a coating blade made of flexible steel, a metal other than chromium that prevents hydrogen absorption is coated near the contact part with the base paper for coating, and the coating is coated with chromium with a thickness of 5 μm or more and the steel material A coating blade characterized by being coated thinner than the thickness of the coating blade.
、ニッケル−リン合金、ニッケル−ホウ素合金、又は銅
であり、3乃至50μmの厚みに被覆したことを特徴と
する請求項1記載の塗工用ブレード。(2) The coating according to claim 1, wherein the metal other than chromium that prevents hydrogen storage is nickel, nickel-phosphorus alloy, nickel-boron alloy, or copper, and is coated to a thickness of 3 to 50 μm. blade.
に対する防食性を有し水素吸蔵を妨げるクロム以外の金
属をブレードの全面に被覆し、該被覆の塗工用原紙との
接触部近傍に、クロムを5μm以上で且つ鋼材の厚みよ
りも薄く被覆したことを特徴とする塗工用ブレード。(3) In a coating blade made of flexible steel, the entire surface of the blade is coated with a metal other than chromium that has anti-corrosion properties against steel and prevents hydrogen absorption, and the contact portion of the coating with the base paper for coating A coating blade characterized in that the vicinity thereof is coated with chromium to a thickness of 5 μm or more and thinner than the thickness of the steel material.
以外の金属は、ニッケル、ニッケル−リン合金、又はニ
ッケル−ホウ素合金のうち少なくとも1つであることを
特徴とする請求項3記載の塗工用ブレード。(4) The coating according to claim 3, wherein the metal other than chromium, which has anti-corrosion properties against steel and prevents hydrogen absorption, is at least one of nickel, nickel-phosphorus alloy, or nickel-boron alloy. Industrial blade.
との接触部近傍に5μm以上であって且つ鋼材の厚みよ
りも薄くクロムを被覆し、次いで110℃〜145℃で
アニールすることを特徴とする塗工用ブレードの製造方
法。(5) The coating blade made of flexible steel is coated with chromium in a thickness of 5 μm or more and thinner than the steel material near the contact area with the coating base paper, and then annealed at 110°C to 145°C. A method for manufacturing a coating blade, characterized by:
くとも塗工用原紙との接触部近傍に電気めっきによりク
ロムを被覆し、電気めっき液の組成は無水クロム酸が1
00〜400g/l、硫酸が無水クロム酸濃度の1/7
0〜1/120量で、液温が35〜65℃でクロム析出
による応力が±15Kg/mm^2以下となるようなめ
っき条件としたことを特徴とする塗工用ブレードの製造
方法。(6) The coating blade made of flexible steel is coated with chromium by electroplating at least the vicinity of the contact area with the coating base paper, and the composition of the electroplating solution is 1 part chromic acid anhydride.
00-400g/l, sulfuric acid is 1/7 of chromic anhydride concentration
A method for manufacturing a coating blade, characterized in that the plating conditions are such that the plating amount is 0 to 1/120, the liquid temperature is 35 to 65°C, and the stress due to chromium precipitation is ±15 Kg/mm^2 or less.
酸、ホウ酸塩、スルファミン酸、アルキルスルホン酸の
うちの少なくとも1つの化合物を加え、その添加量はク
ロムめっき後の研摩を不要とする程度にクロムの平滑性
が得られる範囲としたことを特徴とする請求項6記載の
塗工用ブレードの製造方法。(7) At least one compound selected from fluorosilicic acid, fluorosilicic acid, boric acid, borate, sulfamic acid, and alkyl sulfonic acid is added to the electroplating solution, and the amount of addition is such that polishing is not required after chromium plating. 7. The method for manufacturing a coating blade according to claim 6, wherein the range is such that a certain degree of smoothness of chromium can be obtained.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1199597A JP2583611B2 (en) | 1989-07-31 | 1989-07-31 | Manufacturing method of coating blade |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1199597A JP2583611B2 (en) | 1989-07-31 | 1989-07-31 | Manufacturing method of coating blade |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0364595A true JPH0364595A (en) | 1991-03-19 |
| JP2583611B2 JP2583611B2 (en) | 1997-02-19 |
Family
ID=16410502
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1199597A Expired - Lifetime JP2583611B2 (en) | 1989-07-31 | 1989-07-31 | Manufacturing method of coating blade |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2583611B2 (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1197584A1 (en) * | 2000-10-10 | 2002-04-17 | BTG Eclépens S.A. | Coating blade and process for manufacturing the same |
| WO2002046526A1 (en) * | 2000-12-07 | 2002-06-13 | Swedev Aktiebolag | Doctor or coater blade and method in connection with its manufacturing |
| WO2003064157A1 (en) | 2002-01-29 | 2003-08-07 | Nihon New Chrome Co., Ltd. | Surface treated doctor blade |
| CN100387775C (en) * | 2006-04-13 | 2008-05-14 | 山东科技大学 | Wear-resistant paper coating scraper |
| CN100432333C (en) * | 2006-05-12 | 2008-11-12 | 戴亚洲 | Ceramic coating scraper and its machining process |
| CN101781786A (en) * | 2010-02-24 | 2010-07-21 | 戴亚洲 | Ceramic composite alloy coat ink scraping knife and manufacturing method thereof |
| JP2013019024A (en) * | 2011-07-11 | 2013-01-31 | Hyogo Prefecture | Plated product and plating method |
| JP2014051686A (en) * | 2012-09-04 | 2014-03-20 | Daisho:Kk | Electrogalvanizing processing method and electrogalvanizing processing apparatus |
| KR20180128903A (en) * | 2016-03-31 | 2018-12-04 | 비티지 에클레펜 엣스.에이. | Masked coated blade |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013133762A1 (en) * | 2012-03-08 | 2013-09-12 | Swedev Ab | Electrolytically puls-plated doctor blade with a multiple layer coating |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS498946U (en) * | 1972-04-28 | 1974-01-25 | ||
| JPS5988995A (en) * | 1982-10-13 | 1984-05-23 | インベンテイング・ソシエテ・アノニム | Scraper or blade for controllably applying and leveling coating agent to continuous paper web |
-
1989
- 1989-07-31 JP JP1199597A patent/JP2583611B2/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS498946U (en) * | 1972-04-28 | 1974-01-25 | ||
| JPS5988995A (en) * | 1982-10-13 | 1984-05-23 | インベンテイング・ソシエテ・アノニム | Scraper or blade for controllably applying and leveling coating agent to continuous paper web |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1197584A1 (en) * | 2000-10-10 | 2002-04-17 | BTG Eclépens S.A. | Coating blade and process for manufacturing the same |
| WO2002031220A1 (en) * | 2000-10-10 | 2002-04-18 | BTG Eclépens S.A. | Coating blade and method for making same |
| WO2002046526A1 (en) * | 2000-12-07 | 2002-06-13 | Swedev Aktiebolag | Doctor or coater blade and method in connection with its manufacturing |
| US6841264B2 (en) | 2000-12-07 | 2005-01-11 | Swedev Aktiebolag | Doctor or coater blade and method in connection with its manufacturing |
| WO2003064157A1 (en) | 2002-01-29 | 2003-08-07 | Nihon New Chrome Co., Ltd. | Surface treated doctor blade |
| US7152526B2 (en) | 2002-01-29 | 2006-12-26 | Nihon New Chrome Co., Ltd. | Surface treated doctor blade |
| CN100387775C (en) * | 2006-04-13 | 2008-05-14 | 山东科技大学 | Wear-resistant paper coating scraper |
| CN100432333C (en) * | 2006-05-12 | 2008-11-12 | 戴亚洲 | Ceramic coating scraper and its machining process |
| CN101781786A (en) * | 2010-02-24 | 2010-07-21 | 戴亚洲 | Ceramic composite alloy coat ink scraping knife and manufacturing method thereof |
| JP2013019024A (en) * | 2011-07-11 | 2013-01-31 | Hyogo Prefecture | Plated product and plating method |
| JP2014051686A (en) * | 2012-09-04 | 2014-03-20 | Daisho:Kk | Electrogalvanizing processing method and electrogalvanizing processing apparatus |
| KR20180128903A (en) * | 2016-03-31 | 2018-12-04 | 비티지 에클레펜 엣스.에이. | Masked coated blade |
| JP2019510143A (en) * | 2016-03-31 | 2019-04-11 | ビーティジー・エクレパン・エス.エー.Btg Eclepens S.A. | Masked coating blade |
| US11466407B2 (en) | 2016-03-31 | 2022-10-11 | Btg Eclepens S.A. | Masked coating blade |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2583611B2 (en) | 1997-02-19 |
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