JPS62289274A - Rust prevented steel sheet having excellent workability - Google Patents
Rust prevented steel sheet having excellent workabilityInfo
- Publication number
- JPS62289274A JPS62289274A JP23534386A JP23534386A JPS62289274A JP S62289274 A JPS62289274 A JP S62289274A JP 23534386 A JP23534386 A JP 23534386A JP 23534386 A JP23534386 A JP 23534386A JP S62289274 A JPS62289274 A JP S62289274A
- Authority
- JP
- Japan
- Prior art keywords
- steel sheet
- film
- rust
- excellent workability
- steel plate
- 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
- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 42
- 239000010959 steel Substances 0.000 title claims abstract description 42
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 title abstract description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 21
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000011701 zinc Substances 0.000 claims abstract description 15
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 14
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims abstract description 13
- 239000002131 composite material Substances 0.000 claims abstract description 12
- 238000007747 plating Methods 0.000 claims abstract description 10
- 239000000463 material Substances 0.000 claims abstract description 8
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 8
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 8
- 239000010410 layer Substances 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 12
- 239000011347 resin Substances 0.000 claims description 12
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 10
- 239000011247 coating layer Substances 0.000 claims description 6
- 230000001681 protective effect Effects 0.000 claims 1
- 229920001228 polyisocyanate Polymers 0.000 abstract description 6
- 239000005056 polyisocyanate Substances 0.000 abstract description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract description 4
- 239000007795 chemical reaction product Substances 0.000 abstract description 2
- LHFDSCKKVIUJJV-UHFFFAOYSA-N n-(2-chlorophenyl)methanimine Chemical compound ClC1=CC=CC=C1N=C LHFDSCKKVIUJJV-UHFFFAOYSA-N 0.000 abstract description 2
- 229920001515 polyalkylene glycol Polymers 0.000 abstract description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 abstract description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 26
- 238000012545 processing Methods 0.000 description 19
- 238000005260 corrosion Methods 0.000 description 16
- 230000007797 corrosion Effects 0.000 description 14
- 229920005749 polyurethane resin Polymers 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 150000002440 hydroxy compounds Chemical class 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- -1 amine compound Chemical class 0.000 description 7
- 229920005862 polyol Polymers 0.000 description 7
- 239000000243 solution Substances 0.000 description 6
- 238000004070 electrodeposition Methods 0.000 description 5
- 150000003077 polyols Chemical class 0.000 description 5
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000002390 adhesive tape Substances 0.000 description 3
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 3
- 125000005442 diisocyanate group Chemical group 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000008119 colloidal silica Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000005829 trimerization reaction Methods 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001845 chromium compounds Chemical class 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000001723 curing Methods 0.000 description 1
- UYFMQPGSLRHGFE-UHFFFAOYSA-N cyclohexylmethylcyclohexane;isocyanic acid Chemical class N=C=O.N=C=O.C1CCCCC1CC1CCCCC1 UYFMQPGSLRHGFE-UHFFFAOYSA-N 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000013008 moisture curing Methods 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 229920003226 polyurethane urea Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Electroplating Methods And Accessories (AREA)
Abstract
Description
【発明の詳細な説明】
3、発明の詳細な説明
[産業上の利用分野]
本発明は加工性に優れた防錆鋼板に関し、さらに詳しく
は、自動車用車体、家庭用電化製品、建造物用壁体等に
用いられる加工性に優れた防錆鋼板に関する。[Detailed Description of the Invention] 3. Detailed Description of the Invention [Field of Industrial Application] The present invention relates to a rust-proof steel plate with excellent workability, and more specifically, to a rust-proof steel plate for use in automobile bodies, household appliances, and buildings. This invention relates to a rust-proof steel plate with excellent workability for use in walls, etc.
「伜廿り虹トクr]
従来より防錆鋼板として種々の構成のものが提案され使
用されている。例えば、自動車用の車体に用いる場合に
、通称、シンクロメタルと呼ばれている防錆鋼板が使用
されているが、これは鋼板上にクロム化合物を含む第1
層と亜鉛粉末および樹脂を含むノンフリッチペイントの
塗装の第2層からなるもので(以下ジンクリッチ防錆鋼
板という。)、耐蝕性が良好で、自動車用鋼板としての
条件である電着塗装およびスポット溶接を行なうことが
できろ。``Rainbow Toku R'' Various configurations have been proposed and used as rust-proof steel sheets.For example, when used for automobile bodies, rust-proof steel sheets commonly known as synchro metal are used. is used, but this is the first material containing chromium compounds on the steel plate.
The steel sheet consists of a second layer of non-frich paint containing zinc powder and resin (hereinafter referred to as zinc-rich anti-corrosion steel sheet), and has good corrosion resistance and is coated with electro-deposition and a second layer of non-fitch paint containing zinc powder and resin. Be able to do spot welding.
しかしながら、このジンクリッチ防錆調板は、以下説明
するような問題点がある。However, this zinc-rich rustproofing plate has problems as described below.
(1)耐蝕性と電着塗装性を保障するためには上記第2
層に亜鉛粉末が80wt%以上含ま以上−るため、プレ
ス加工等の際皮膜が粉末状に剥離し、加工傷の原因とな
る。(1) In order to ensure corrosion resistance and electrodeposition coating properties, the above-mentioned second
Since the layer contains 80 wt % or more of zinc powder, the film peels off in powder form during press working, etc., causing processing scratches.
(2)ジンクリッチ皮膜が、例えば10μm以上と厚く
塗装されている場合には、亜鉛粉末および樹脂が多量に
存在するため、連続スポット溶接による亜鉛および樹脂
の燃焼残渣によって電極チップが汚染され、チップドレ
ッシング頻度が増大し、作業性の劣化を招来する。(2) If the zinc-rich film is applied thickly, for example 10 μm or more, large amounts of zinc powder and resin will be present, and the electrode tip will be contaminated by the combustion residue of zinc and resin from continuous spot welding. Dressing frequency increases, leading to deterioration of workability.
しかし、このような上記のジンクリッチ防錆鋼板の問題
点を考慮した防錆鋼板についつ、特開昭58−0981
72号公報および特開昭57−108292号公報には
、1μm程度の有機複合シリケート皮膜を形成した防錆
鋼板が提案されているが、これら公報に示されている防
錆鋼板は、複合ソリケートを主成分とする皮膜中にMO
lW、■、Sn、B5Siの酸素酸またはアルコキシド
キレート化合物を含むことを必須としており、また、ウ
レタン系rf機複合シリケートは含まれていない。However, regarding a rust-proof steel plate that takes into consideration the above-mentioned problems of the zinc-rich rust-proof steel plate, Japanese Patent Application Laid-Open No. 58-0981
No. 72 and Japanese Unexamined Patent Publication No. 108292/1987 propose rust-preventing steel sheets with an organic composite silicate film of about 1 μm. MO in the film that is the main component
It is essential to contain oxyacid or alkoxide chelate compounds of lW, ■, Sn, and B5Si, and does not contain urethane-based RF machine composite silicate.
そして、このような防錆鋼板は厳しい加工条件、例えば
、ドロービードテストおよび例えば、電着塗装+中塗り
士」二塗り等の塗装後の各種密着性テスト等においては
、皮膜密着性が充分でないという問題がある。In addition, such rust-proof steel sheets do not have sufficient film adhesion under severe processing conditions, such as drawbead tests and various adhesion tests after painting, such as two coats of electrodeposition and intermediate coating. There is a problem.
[発明′)<解決しようとずろ問題点]本発明は上記に
説明したような従来における防錆鋼板における種々の問
題点に鑑みなされたものであり、本発明者が鋭意研究を
行なった結果、優れた皮膜密着性を有する加工性に優れ
た防錆鋼板を開発したのである。[Invention') <Problems to be solved] The present invention was made in view of the various problems in conventional rust-proof steel plates as explained above, and as a result of intensive research by the present inventor, We have developed a rust-proof steel sheet with excellent film adhesion and excellent workability.
[問題点を解決するための手段]
本発明に係る加工性に優れた防p!鋼板は、(1)!i
板上に設けられた亜鉛系めっき層の上に、ウレタン系樹
脂および二酸化珪素の複合物質または混合物質を主成分
とする皮膜層を設けたことを特徴とする加工性に優れた
防錆鋼板を第1の発明とし、
(2)jI!i板上に設けられた亜鉛系めっき層の上に
、ウレタン系樹脂および二酸化珪素の複合物質または混
合物質に亜鉛粉末を含有させた物質を主成分とする皮膜
層を設けたことを特徴とする加工性に優れた防錆鋼板を
第2の発明とする2つの発明よりなるものである。[Means for solving the problems] The p-proof film with excellent workability according to the present invention! Steel plate is (1)! i
A rust-proof steel sheet with excellent workability, which is characterized by having a coating layer mainly composed of a composite material or a mixture of urethane resin and silicon dioxide on the zinc-based plating layer provided on the sheet. As the first invention, (2) jI! A film layer whose main component is a composite material or mixed material of urethane resin and silicon dioxide containing zinc powder is provided on the zinc plating layer provided on the i-board. This invention consists of two inventions, with the second invention being a rust-proof steel plate with excellent workability.
なお、必要に応じて亜鉛系めっき層とウレタン樹脂およ
び二酸化珪素の複合物質または混合物質を主成分とする
皮膜層との間にクロメート層を形成してもよい。Note that, if necessary, a chromate layer may be formed between the zinc-based plating layer and the coating layer whose main component is a composite material or mixed material of urethane resin and silicon dioxide.
また、種々の防錆顔料を上記皮膜層中に共存さUて耐蝕
性をより向上させることができ、さらに、Zn粉末を添
加して皮膜層に導電性を付与し、かつ、耐蝕性を向上さ
せることができる。In addition, various anti-corrosion pigments can be coexisted in the coating layer to further improve corrosion resistance, and Zn powder can be added to impart conductivity to the coating layer and improve corrosion resistance. can be done.
本発明に係る加工性に優れた防錆鋼板に使用される亜鉛
系めっき層を設けた鋼板としては、亜鉛単層めっき綱板
、亜鉛合金めっき鋼板およびこれらの多層めっき鋼板を
挙げることができる。Examples of the steel sheet provided with a zinc-based plating layer used in the rust-proof steel sheet with excellent workability according to the present invention include a single-layer zinc-plated steel sheet, a zinc alloy-plated steel sheet, and a multilayer-plated steel sheet thereof.
皮膜層には、樹脂成分としてウレタン系樹脂或いはウレ
タン系樹脂と曲の樹脂、例えば、エボキン、アクリル、
フェノール等の各樹脂との混合物を乎げることかできる
。The film layer contains urethane resin or urethane resin and resin such as evokin, acrylic, etc. as resin components.
It is also possible to prepare a mixture with various resins such as phenol.
このウレタン系樹脂と二酸化珪素はシリコンカップリン
グ剤により複合物質としてもよく、また、混合物質とし
てもよい。This urethane resin and silicon dioxide may be made into a composite material using a silicon coupling agent, or may be made into a mixed material.
ここにいうボウレタン樹脂とは、有機ポリカーボネート
と多価ヒドロキシ化合物および多価アミン化合物との反
応物である。The bouletane resin referred to herein is a reaction product of an organic polycarbonate, a polyvalent hydroxy compound, and a polyvalent amine compound.
T子機ポリイソノアネートとしては、
トリレンジイソシアネート、ノフェニルメタンジイソン
アネート、ポリメチレンポリフェニルイソシアネート、
ヘキサメチレンジイソンアネート、キンリレンジイソシ
アネート、ナフタリンジイソシアネート、トリジンジイ
ソシアネート、イソホロンジイソシアネート、水添キン
リレンジイソシアネート、水添ジシクロヘキシルメタン
ジイソシアネート等の脂肪族、芳香族、指環族イソシア
ネートおよびこれらの三量化、三量化物がある。T child unit polyisonoanate includes tolylene diisocyanate, nophenylmethane diisonanate, polymethylene polyphenylisocyanate,
Aliphatic, aromatic, ring group isocyanates such as hexamethylene diisonanate, quinlylene diisocyanate, naphthalene diisocyanate, toridine diisocyanate, isophorone diisocyanate, hydrogenated quinlylene diisocyanate, hydrogenated dicyclohexylmethane diisocyanate, and their trimerization and trimerization products There is.
多価ヒドロキシ化合物としては、
ポリアルキレングリコール、ポリアミンポリオール、ポ
リマーポリオール、ポリテトラメチレングリコール等の
ポリエーテル系ポリオール、アジペート系ポリオール、
フタル酸系ポリオール、ポリカプロラクトン系ポリオー
ル、ポリカーボネート系ポリオール等のポリエステル系
ポリオール、トリメチロールプロパン、ブタンジオール
等の多価アルコール化合物等がある。Examples of polyhydric hydroxy compounds include polyalkylene glycols, polyamine polyols, polymer polyols, polyether polyols such as polytetramethylene glycol, adipate polyols,
Examples include polyester polyols such as phthalic acid polyols, polycaprolactone polyols, and polycarbonate polyols, and polyhydric alcohol compounds such as trimethylolpropane and butanediol.
多価アミノ化合物としては、
メチレンオルソクロロアニリン、ジアミノジフェニルメ
タン、エチレンノアミン、ジエチレントリアミン、ヒド
ラジン、イソホロンジアミン、トリエチレンテトラミン
等がある。Examples of polyvalent amino compounds include methylene orthochloroaniline, diaminodiphenylmethane, ethylenenoamine, diethylenetriamine, hydrazine, isophoronediamine, and triethylenetetramine.
ポリウレタン樹脂を加工法的に大別すると、(1)各種
有機ポリイソシアネート、多価ヒドロキシ化合物の重合
反応により、ウレタンプレポリマーを合成し、加工時に
多価アミノ化合物、多価ヒドロキシ化合物、湿気等で樹
脂化する熱硬化(常温硬化)性ポリウレタン樹脂。Polyurethane resins can be broadly categorized based on processing methods: (1) Urethane prepolymers are synthesized through polymerization reactions of various organic polyisocyanates and polyvalent hydroxy compounds, and during processing, polyurethane prepolymers are synthesized using polyvalent amino compounds, polyvalent hydroxy compounds, moisture, etc. A thermosetting (room temperature curing) polyurethane resin that turns into a resin.
(2)各種有機ポリイソシアネート、多価ヒドロキシ化
合物、多価アミノ化合物等を加工時に混合樹脂化するワ
ンシ式ットボリウレタン樹脂。(2) One-piece polyurethane resin that converts various organic polyisocyanates, polyvalent hydroxy compounds, polyvalent amino compounds, etc. into a mixed resin during processing.
(3)各種有機ポリイソシアネート、多価ヒドロキシ化
合物の重合反応によりウレタンプレポリマーあるいは、
ポリウレタン樹脂を各種溶媒中に溶解希釈した溶媒揮散
型(一部湿気硬化型を含む)ポリウレタン樹脂。(3) Urethane prepolymer or
Solvent volatilization type (including some moisture curing type) polyurethane resins made by dissolving and diluting polyurethane resins in various solvents.
(4)各種有機ポリイソシアネート、多価ヒドロキシ化
合物の重合反応により得られたポリウレタン樹脂を加工
時に熱溶融する熱可塑型ポリウレタン樹脂。(4) Thermoplastic polyurethane resin that is obtained by thermally melting polyurethane resin obtained by polymerization reaction of various organic polyisocyanates and polyhydric hydroxy compounds during processing.
(5)各種有機ポリイソシアネート、多価ヒドロキシ化
合物の重合反応の際、親水性基を導入して得られるポリ
ウレタン樹脂、あるいは、ウレタンプレポリマーを水中
に乳化するか、または、各種有機ポリイソシアネート、
多価ヒドロキシ化合物の重合反応により得られたポリウ
レタン樹脂、あるいは、ウレタンプレポリマーを界面活
性剤かコロイド剤を用いて、強制的に乳化する水添系ポ
リウレタン樹脂。(5) Various organic polyisocyanates, polyurethane resins obtained by introducing hydrophilic groups during the polymerization reaction of polyhydric hydroxy compounds, or urethane prepolymers are emulsified in water, or various organic polyisocyanates,
A hydrogenated polyurethane resin obtained by forcibly emulsifying a polyurethane resin obtained by the polymerization reaction of a polyhydric hydroxy compound or a urethane prepolymer using a surfactant or colloid agent.
等がある。etc.
[実施例] 本発明に係る加工性に優れた防錆の実施例を説明する。[Example] An example of rust prevention with excellent workability according to the present invention will be described.
実施例1
減圧脱水したポリテトラメチレンエーテルグリコール(
OH,V、55J)202部に101部のメチルエチル
ケトンを加えて均一に混合した後、2゜4−および2,
6トリレンジイソシアネート80:20の混合物34.
8部を加えて、80℃の温度で2時間反応させ、2.4
8%のイソシアネート基を含有するウレタンプレポリマ
ー溶液を得た。Example 1 Polytetramethylene ether glycol dehydrated under reduced pressure (
After adding 101 parts of methyl ethyl ketone to 202 parts of OH, V, 55J) and mixing uniformly, 2°4- and 2,
6 tolylene diisocyanate 80:20 mixture 34.
Add 8 parts and react at a temperature of 80°C for 2 hours to obtain 2.4
A urethane prepolymer solution containing 8% isocyanate groups was obtained.
別の反応器に600部のメチルエチルケトンと10.7
部のジエチレントリアミンを入れて均一に混合し、この
溶液のなかに、上記のウレタンプレポリマー溶液300
部をlO〜20℃温度で徐々に滴下して加え、ついで5
0℃の温度で30分間反応して、ポリウレタン尿素ポリ
アミン溶液を得た。In a separate reactor, 600 parts of methyl ethyl ketone and 10.7
300% of the above urethane prepolymer solution is added to this solution and mixed uniformly.
10 parts dropwise at a temperature of 10 to 20°C, then 5 parts
A polyurethaneurea polyamine solution was obtained by reacting at a temperature of 0° C. for 30 minutes.
ついで、この溶液にトリメット酸無水物25.8部を加
え、均一に溶解させた後、50℃の温度に昇温しで30
分間反応させた。Next, 25.8 parts of trimet acid anhydride was added to this solution, and after uniformly dissolving it, the temperature was raised to 50°C and the temperature was increased to 30°C.
Allowed to react for minutes.
続いて、水650部にl008部の水酸化ナトリウムを
溶解した水溶液を加えて、減圧下にメチルエチルケトン
を留去し、水を加えて樹脂分を調整し、濃度30%のエ
マルジョンを得た。Subsequently, an aqueous solution of 1,008 parts of sodium hydroxide dissolved in 650 parts of water was added, methyl ethyl ketone was distilled off under reduced pressure, and water was added to adjust the resin content to obtain an emulsion with a concentration of 30%.
この水溶性ウレタンエマルジョン(固形成分30%)
: 100重量部コロイグルシリ力
(Sing 40wt%、): 50重量部
を混合して塗液を作成した。This water-soluble urethane emulsion (30% solids)
: 100 parts by weight Coroiglue strength (Sing 40 wt%): 50 parts by weight were mixed to prepare a coating liquid.
次いで、この塗液を、脱脂処理およびクロメート処理(
無水クロム酸水溶液塗布、195℃/30秒乾燥、全ク
ロム150mg/mつを施したZn−12%Niめっき
鋼板(めっき厚20g/曽2)に、バーコーターで塗布
し、炉温200℃で1分間焼付けることにより、5iO
y/ウレタン樹脂=0.40、平均膜厚1.5μmの皮
膜層か形成された防錆鋼板を製造した。Next, this coating liquid is subjected to degreasing treatment and chromate treatment (
Chromic anhydride aqueous solution applied, dried at 195°C for 30 seconds, coated with a bar coater on a Zn-12%Ni plated steel plate (plating thickness 20g/so2) with a total chromium content of 150mg/m2, and heated at a furnace temperature of 200°C. By baking for 1 minute, 5iO
A rust-preventive steel plate was produced in which a coating layer was formed with y/urethane resin=0.40 and an average thickness of 1.5 μm.
このようにして製造された防錆鋼板について、(1)3
コート後の皮膜密着性試験
(2)加工時の皮膜剥離性および加工後の耐蝕性試験
を行なった。Regarding the rust-proof steel plate manufactured in this way, (1) 3
Film adhesion test after coating (2) Film peelability during processing and corrosion resistance test after processing were conducted.
(I)3コート後の皮膜密着性試験
本発明に係る加工性に優れた防錆鋼板にカチオン電着塗
料15μm、自動車用中塗り35μm、自動車用上塗り
35μmの合計85μmの塗装を行ない、50℃温水に
240時間浸漬後2闘基盤目粘着テープ端豹ル丘r?う
ト一
その結果、皮膜剥離は認められなかった。(I) Film adhesion test after 3 coats The rust-preventive steel sheet with excellent workability according to the present invention was coated with a total of 85 μm of cationic electrodeposition paint of 15 μm, an automotive intermediate coat of 35 μm, and an automotive top coat of 35 μm at 50°C. After soaking in hot water for 240 hours, the adhesive tape ends on the second base. As a result, no peeling of the film was observed.
(2)加工時の皮膜剥離性および加工後の耐蝕性試験
第1図に示すドロービード試験装置を用いて加工時の皮
膜剥離性を調査した。(2) Film removability during processing and corrosion resistance test after processing The film removability during processing was investigated using the drawbead test device shown in FIG.
引張速度300 mm/min、伸びを20%とした。The tensile speed was 300 mm/min, and the elongation was 20%.
テスト後の摺動部の粘着テープ剥離試験による皮膜剥型
は0 、1 g/m″以下であった。After the test, the adhesive tape peeling test of the sliding part showed that the film peeled off was less than 0.1 g/m''.
このドロービード試験後の耐蝕性を以下に示すサイクル
試験により調査した。The corrosion resistance after this drawbead test was investigated by the cycle test shown below.
塩水噴霧試験(35℃×4時間)−乾燥(60℃×2時
間)−湿潤(50℃×2時間)−塩水噴霧試験というサ
イクルを8時間/1サイクルで行なった。A cycle of salt water spray test (35° C. x 4 hours) - drying (60° C. x 2 hours) - wet (50° C. x 2 hours) - salt water spray test was carried out for 8 hours/1 cycle.
200サイクル後の摺動部210cm’当りの最大腐蝕
深さは75μmであった。The maximum corrosion depth per 210 cm' of sliding portion after 200 cycles was 75 μm.
2比較例I
水性アクリルエマルジョン(固形成分30%)を使用し
、実施例1と同じ方法により処理し、平均膜厚1.5μ
mの有機複合シリケート(Sift/アクリル樹[1−
0,40)皮膜を形成した。2 Comparative Example I Using an aqueous acrylic emulsion (solid content 30%), treated by the same method as Example 1, average film thickness 1.5μ
m organic composite silicate (Sift/acrylic tree [1-
0,40) A film was formed.
実施例1と同じ方法で性能試験を行なった。A performance test was conducted in the same manner as in Example 1.
(1)3コート後の皮膜密着性試験 皮膜の75%が剥離した。(1) Film adhesion test after 3 coats 75% of the film was peeled off.
(2)加工時の皮膜剥離性および加工後の耐蝕性皮膜剥
離性 3.5g/m’最大腐蝕深さ
560μm
実施例2
水性ウレタンエマルジョン(固形成分30%)、 10
0重量部
コロイダルシリカ(SiOt 40%); 50重量
部
亜鉛粉末 = 60重量部γ−アミノプロ
ピルトリエトキシシラン: 9重量部
蒸留水 : 300重量部を混合してチ
液を作製した。(2) Film removability during processing and corrosion-resistant film removability after processing 3.5 g/m' maximum corrosion depth
560 μm Example 2 Aqueous urethane emulsion (solid content 30%), 10
0 parts by weight colloidal silica (SiOt 40%); 50 parts by weight zinc powder = 60 parts by weight γ-aminopropyltriethoxysilane: 9 parts by weight Distilled water: 300 parts by weight were mixed to prepare a broth.
実施例1と同様にクロメート処理を行ない、バーコータ
ー塗装により亜鉛粉を50wt%含有するa機複合ンリ
ケート皮膜(平均膜厚3.5μm)を得た。Chromate treatment was carried out in the same manner as in Example 1, and a composite phosphoric acid film containing 50 wt % zinc powder (average film thickness 3.5 μm) was obtained by coating with a bar coater.
こうして製造された防錆鋼板について実施例1と同様な
方法で性能試験を行なった。A performance test was conducted using the same method as in Example 1 for the rust-proof steel sheet manufactured in this way.
(1) 3コート後の皮膜密着性試験 皮膜の剥離は認められなかった。(1) Film adhesion test after 3 coats No peeling of the film was observed.
(2)加工時の皮膜剥離性および加工後の耐蝕性試験
皮膜剥離’j1 0.Ig/m’以下
最大腐蝕深さ 20μm実施例3
溶剤系ポリウレタン樹脂(固形成分IO%): 10
0重量部
微粉末5iO2(平均粒径0.5μm) : 5ff
iff1部ンメヂルスルフ十アミド : 100重量
部を混合して塗液を作成した。(2) Film peelability during processing and corrosion resistance test after processing Film peeling 'j1 0. Ig/m' or less Maximum corrosion depth 20 μm Example 3 Solvent-based polyurethane resin (solid content IO%): 10
0 parts by weight Fine powder 5iO2 (average particle size 0.5 μm): 5ff
A coating liquid was prepared by mixing 1 part of IF and 100 parts by weight of medyl sulfur amide.
次いで、このQ液を脱酸処理およびクロメート処理(無
水クロム酸とコロイダルシリカ混合液塗布、200℃X
30 sec乾燥、全クロム量50mg/mりを施し
たZn−12%Niめっき鋼板(めっき厚20g/mつ
にバーコーターで塗布し、炉温200℃で1分間焼付け
ることにより5iOy/ウレタン樹脂−0,5、平均膜
厚=0.8μmの皮膜層を育する防錆鋼板を製造した。Next, this Q solution was deoxidized and chromated (chromic anhydride and colloidal silica mixed solution applied, 200°C
Zn-12%Ni plated steel plate with a total chromium content of 50 mg/m after drying for 30 seconds (coated with a bar coater to a plating thickness of 20 g/m and baked at a furnace temperature of 200°C for 1 minute to form 5iOy/urethane resin) -0.5, a rust-preventive steel plate with a film layer of average film thickness = 0.8 μm was manufactured.
このようにして製造された防錆鋼板について以下説明ず
ろ試験を行った。The rust-proof steel sheet manufactured in this way was subjected to a shear test as described below.
(I)3コート後の皮膜密着性試験
本発明に係る加工生に優れた防錆鋼板に、カチオン電着
塗料15μm、自動車中塗り塗料35μm、同上塗り塗
料35μmの合計85μmの塗装を行い、50℃の温水
に240時間浸漬後2mmゴバン目枯着テープ試験を行
った。(I) Film adhesion test after 3 coats The anticorrosive steel sheet according to the present invention, which has excellent processing properties, was coated with a total of 85 μm of cationic electrodeposition paint of 15 μm, automotive intermediate coating of 35 μm, and the same top coat of 35 μm. After immersion in warm water at ℃ for 240 hours, a 2 mm thick drying tape test was conducted.
この結果、皮膜剥離は認められなかった。As a result, no peeling of the film was observed.
(2)加工時の皮膜剥離性および加工後の耐蝕性試験
第1図に示すドロービード試験装置を用いて加工時の皮
膜剥離性を調査した。(2) Film removability during processing and corrosion resistance test after processing The film removability during processing was investigated using the drawbead test device shown in FIG.
引張速度 300 mm/ ff1in、伸びを20%
とした。Tensile speed 300 mm/ff1in, elongation 20%
And so.
試験後の摺動部の粘着テープ剥離試験による皮膜剥離量
は0.1g/m″以下であった。After the test, the amount of film peeled off from the adhesive tape peeling test of the sliding part was 0.1 g/m'' or less.
このドロービード試験後の耐蝕性を実施例!で実施した
のと同じサイクルテストにより評価した。An example of corrosion resistance after this drawbead test! The evaluation was carried out using the same cycle test as that carried out in .
200サイクル後の摺動部210cm当たりの最大浸蝕
深さは85μmであった。The maximum erosion depth per 210 cm of sliding portion after 200 cycles was 85 μm.
[発明の効果]
以上説明したように、本発明に係る加工性に優れた防錆
鋼板は上記の構成であるから、加工に際しての皮膜密着
性に優れた防錆鋼板である。[Effects of the Invention] As explained above, since the rust-proof steel plate with excellent workability according to the present invention has the above-mentioned configuration, it is a rust-proof steel plate with excellent film adhesion during processing.
第1図はドロービード試験装置の説明図である。 之1 力 300丁僑 FIG. 1 is an explanatory diagram of a drawbead test device. No.1 Power 300 people
Claims (2)
タン系樹脂および二酸化珪素の複合物質または混合物質
を主成分とする皮膜層を設けたことを特徴とする加工性
に優れた防錆鋼板。(1) A protective film with excellent workability characterized by having a coating layer mainly composed of a composite material or mixed material of urethane resin and silicon dioxide on the zinc-based plating layer provided on the steel sheet. Rusty steel plate.
タン系樹脂および二酸化珪素の複合物質または混合物質
に亜鉛粉末を含有させた物質を主成分とする皮膜層を設
けたことを特徴とする加工性に優れた防錆綱板。(2) On top of the zinc-based plating layer provided on the steel plate, a film layer whose main component is a composite material or mixed material of urethane-based resin and silicon dioxide containing zinc powder is provided. Rust-proof steel plate with excellent workability.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61-27477 | 1986-02-10 | ||
JP2747786 | 1986-02-10 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62289274A true JPS62289274A (en) | 1987-12-16 |
JPH067950B2 JPH067950B2 (en) | 1994-02-02 |
Family
ID=12222196
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61235343A Expired - Fee Related JPH067950B2 (en) | 1986-02-10 | 1986-10-02 | Anti-corrosion steel plate for electrodeposition coating that has excellent film adhesion during processing and corrosion resistance after processing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH067950B2 (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01219193A (en) * | 1988-02-25 | 1989-09-01 | Nippon Steel Corp | Production of white chemical conversion-treated galvanized steel sheet |
JPH02124997A (en) * | 1988-07-29 | 1990-05-14 | Kobe Steel Ltd | Surface treating agent and surface-treated steel sheet |
US4959277A (en) * | 1988-12-07 | 1990-09-25 | Nihon Parkerizing Co., Ltd. | Process for treating plated steel sheet |
US5147729A (en) * | 1989-03-31 | 1992-09-15 | Kawasaki Steel Corporation | Steel plate with organic coating having improved corrosion resistance in as-worked state |
US5514483A (en) * | 1992-08-17 | 1996-05-07 | Kawasaki Steel Corporation | Organic composite coated steel plates having improved corrosion resistance in as-worked state |
EP0745434A1 (en) | 1995-05-30 | 1996-12-04 | Kawasaki Steel Corporation | Organic composite coated steel sheet and method |
US6770373B1 (en) | 1998-12-25 | 2004-08-03 | Henkel Corporation | Water-based metal surface treatment composition for forming lubricating film with excellent marring resistance |
JP2010525094A (en) * | 2007-04-19 | 2010-07-22 | アクゾ ノーベル コーティングス インターナショナル ビー ヴィ | Coating composition for metal substrates |
JP2013072560A (en) * | 2011-09-26 | 2013-04-22 | Daikin Industries Ltd | Outer wall panel of air conditioning outdoor unit |
CN109134815A (en) * | 2018-08-14 | 2019-01-04 | 陕西科技大学 | A kind of hard section contains two kinds of heteroatomic polyurethane elastomers, modified polyurethane anticorrosion peelable film and its preparation method and application |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5546097B2 (en) | 2006-06-23 | 2014-07-09 | 新日鐵住金株式会社 | Surface treatment metal material and metal surface treatment agent |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50157426A (en) * | 1973-12-21 | 1975-12-19 | ||
JPS5562973A (en) * | 1978-10-31 | 1980-05-12 | Kansai Paint Co Ltd | Aqueous curable coating composition |
JPS5599976A (en) * | 1979-01-25 | 1980-07-30 | Kansai Paint Co Ltd | Hydrophilic treatment of metal surface |
JPS57105344A (en) * | 1980-12-24 | 1982-06-30 | Nippon Kokan Kk | Surface treating steel plate for painting foundation |
JPS57127479A (en) * | 1981-01-30 | 1982-08-07 | Nisshin Steel Co Ltd | Production of blister resistant painted steel plate |
JPS58147351A (en) * | 1982-02-26 | 1983-09-02 | 新日本製鐵株式会社 | Single side pre-painted steel plate |
JPS58224174A (en) * | 1982-06-23 | 1983-12-26 | Nippon Kokan Kk <Nkk> | Production of coated steel plate having high resistance to corrosion and rust |
JPS6160886A (en) * | 1984-08-31 | 1986-03-28 | Nippon Kokan Kk <Nkk> | Rustproof lubricated steel sheet |
-
1986
- 1986-10-02 JP JP61235343A patent/JPH067950B2/en not_active Expired - Fee Related
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50157426A (en) * | 1973-12-21 | 1975-12-19 | ||
JPS5562973A (en) * | 1978-10-31 | 1980-05-12 | Kansai Paint Co Ltd | Aqueous curable coating composition |
JPS5599976A (en) * | 1979-01-25 | 1980-07-30 | Kansai Paint Co Ltd | Hydrophilic treatment of metal surface |
JPS57105344A (en) * | 1980-12-24 | 1982-06-30 | Nippon Kokan Kk | Surface treating steel plate for painting foundation |
JPS57127479A (en) * | 1981-01-30 | 1982-08-07 | Nisshin Steel Co Ltd | Production of blister resistant painted steel plate |
JPS58147351A (en) * | 1982-02-26 | 1983-09-02 | 新日本製鐵株式会社 | Single side pre-painted steel plate |
JPS58224174A (en) * | 1982-06-23 | 1983-12-26 | Nippon Kokan Kk <Nkk> | Production of coated steel plate having high resistance to corrosion and rust |
JPS6160886A (en) * | 1984-08-31 | 1986-03-28 | Nippon Kokan Kk <Nkk> | Rustproof lubricated steel sheet |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01219193A (en) * | 1988-02-25 | 1989-09-01 | Nippon Steel Corp | Production of white chemical conversion-treated galvanized steel sheet |
JPH02124997A (en) * | 1988-07-29 | 1990-05-14 | Kobe Steel Ltd | Surface treating agent and surface-treated steel sheet |
US4959277A (en) * | 1988-12-07 | 1990-09-25 | Nihon Parkerizing Co., Ltd. | Process for treating plated steel sheet |
US5147729A (en) * | 1989-03-31 | 1992-09-15 | Kawasaki Steel Corporation | Steel plate with organic coating having improved corrosion resistance in as-worked state |
US5514483A (en) * | 1992-08-17 | 1996-05-07 | Kawasaki Steel Corporation | Organic composite coated steel plates having improved corrosion resistance in as-worked state |
EP0745434A1 (en) | 1995-05-30 | 1996-12-04 | Kawasaki Steel Corporation | Organic composite coated steel sheet and method |
US6770373B1 (en) | 1998-12-25 | 2004-08-03 | Henkel Corporation | Water-based metal surface treatment composition for forming lubricating film with excellent marring resistance |
JP2010525094A (en) * | 2007-04-19 | 2010-07-22 | アクゾ ノーベル コーティングス インターナショナル ビー ヴィ | Coating composition for metal substrates |
JP2013072560A (en) * | 2011-09-26 | 2013-04-22 | Daikin Industries Ltd | Outer wall panel of air conditioning outdoor unit |
CN109134815A (en) * | 2018-08-14 | 2019-01-04 | 陕西科技大学 | A kind of hard section contains two kinds of heteroatomic polyurethane elastomers, modified polyurethane anticorrosion peelable film and its preparation method and application |
CN109134815B (en) * | 2018-08-14 | 2020-12-04 | 陕西科技大学 | A kind of polyurethane elastomer containing two kinds of heteroatoms in hard segment, modified polyurethane anti-corrosion peelable film and preparation method and application thereof |
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