JP2003019768A - Coating-type steel sheet reinforcing material - Google Patents
Coating-type steel sheet reinforcing materialInfo
- Publication number
- JP2003019768A JP2003019768A JP2001209604A JP2001209604A JP2003019768A JP 2003019768 A JP2003019768 A JP 2003019768A JP 2001209604 A JP2001209604 A JP 2001209604A JP 2001209604 A JP2001209604 A JP 2001209604A JP 2003019768 A JP2003019768 A JP 2003019768A
- Authority
- JP
- Japan
- Prior art keywords
- reinforcing material
- coating
- steel sheet
- epoxy resin
- reinforcing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000012779 reinforcing material Substances 0.000 title claims abstract description 67
- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 34
- 239000010959 steel Substances 0.000 title claims abstract description 34
- 239000011248 coating agent Substances 0.000 claims description 38
- 238000000576 coating method Methods 0.000 claims description 38
- 239000004593 Epoxy Substances 0.000 claims description 15
- 239000003973 paint Substances 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 abstract description 20
- 239000000463 material Substances 0.000 abstract description 12
- 238000000034 method Methods 0.000 abstract description 12
- 230000003014 reinforcing effect Effects 0.000 abstract description 9
- 239000000945 filler Substances 0.000 abstract description 7
- 238000003825 pressing Methods 0.000 abstract description 5
- 239000000049 pigment Substances 0.000 abstract description 4
- 239000004606 Fillers/Extenders Substances 0.000 abstract description 3
- 229920006334 epoxy coating Polymers 0.000 abstract description 2
- 239000000155 melt Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 description 34
- 238000001723 curing Methods 0.000 description 30
- 239000003822 epoxy resin Substances 0.000 description 23
- 229920000647 polyepoxide Polymers 0.000 description 23
- 239000000654 additive Substances 0.000 description 12
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 8
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 8
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 8
- 239000003085 diluting agent Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000003921 oil Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 230000000996 additive effect Effects 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 238000005406 washing Methods 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 description 4
- 238000013007 heat curing Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 230000002787 reinforcement Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000010422 painting Methods 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 2
- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 2
- 239000002253 acid Substances 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
- 230000007547 defect Effects 0.000 description 2
- 238000005238 degreasing Methods 0.000 description 2
- 239000000539 dimer Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- -1 Aliphatic amines Chemical class 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 208000005189 Embolism Diseases 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000004040 coloring Methods 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
- 238000010276 construction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 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
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003230 hygroscopic agent Substances 0.000 description 1
- 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 1
- 150000003951 lactams Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000013001 point bending Methods 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、主として自動車用
鋼板に使用される塗布型補強材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a coating type reinforcing material mainly used for automobile steel sheets.
【0002】[0002]
【従来の技術】自動車工業における車両重量の軽減化は
常に重要課題となっており、自動車に使用される鋼板も
安全上、構造上の要求を満たす限界まで薄くされてき
た。このため、特に自動車の外側を形成する鋼板には、
鋼板補強材、通常デント材と呼ばれる材料が自動車の内
側部分に貼着され、あるいは熱融着されて、鋼板の剛性
の向上に寄与している。2. Description of the Related Art Reducing vehicle weight in the automobile industry has always been an important issue, and steel sheets used in automobiles have been thinned to the limit of safety and structural requirements. For this reason, especially for the steel plate forming the outside of the automobile,
A steel plate reinforcing material, which is usually called a dent material, is attached to an inner portion of an automobile or heat-sealed to contribute to improvement of rigidity of the steel sheet.
【0003】これらの補強材は、ゴム系、瀝青系、アル
キド樹脂、エポキシ樹脂、ウレタン樹脂、ユリア樹脂等
の合成樹脂系材料に、適宜充填材、添加剤を配合して混
合、混練りし、従来公知の加工方法によって所望の大き
さ、形状に加工し、鋼板の必要部位に貼着されている。These reinforcing materials are rubber-based, bituminous-based, synthetic resin-based materials such as alkyd resin, epoxy resin, urethane resin, urea resin, etc., which are appropriately mixed with fillers and additives, and mixed and kneaded. It is processed into a desired size and shape by a conventionally known processing method and is attached to a necessary portion of a steel plate.
【0004】その中で、成形物の補強材では貼着が困難
な箇所への補強材の施工、あるいは、より軽量な補強材
の開発等、需要者の要求に応えて、本出願人から、塗布
型鋼板補強組成物に関する発明を特願平5−11524
3号として出願している。[0004] Among them, the applicant of the present invention has responded to the demands of the customers, such as the construction of a reinforcing material in a place where it is difficult to attach the molded material by a reinforcing material, or the development of a lighter reinforcing material. An invention relating to a coating type steel plate reinforcing composition is disclosed in Japanese Patent Application No. 11524/1993.
I am applying for No. 3.
【0005】[0005]
【発明が解決しようとする課題】上記発明では、塗布型
にすることにより、必要な部位へ必要量のみの補強材の
施工を可能にしたことで施工に無駄がなくなり、また、
補強材の施工を塗装ロボットや自動塗装機で行なうこと
で、施工の省人化を実現している。In the above-mentioned invention, since the application type is adopted, it is possible to apply only the required amount of the reinforcing material to the required site, and thus the waste is eliminated in the operation, and
Labor saving has been achieved by using a painting robot or automatic painting machine to apply the reinforcing material.
【0006】しかしながら、上記発明になる塗布型補強
材は、加熱硬化型樹脂を使用しているため、自動車のプ
レス工程において塗布されてから、化成処理工程に至る
過程においては未だ加熱を受けておらず、未硬化状態で
ある。このため、補強材が塗布された自動車ボディが化
成処理液に浸漬されると、未硬化の補強材から無機軽量
充填材や体質顔料などが溶け出し、化成処理液を汚染す
るという問題を起こす可能性があった。そこで本発明に
おいては、上記発明の問題点を解決し、更なる鋼板補強
効果、また軽量な補強材の開発を目的とする。However, since the coating type reinforcing material according to the present invention uses the thermosetting resin, it is still heated in the process from the coating in the pressing process of the automobile to the chemical conversion treatment process. No, it is in an uncured state. For this reason, when an automobile body coated with a reinforcing material is dipped in a chemical conversion treatment solution, inorganic lightweight fillers and extender pigments may dissolve from the uncured reinforcement material, which may cause a problem of contaminating the chemical conversion treatment solution. There was a nature. Therefore, the present invention aims to solve the above-mentioned problems of the invention and to develop a steel plate reinforcing effect and a lightweight reinforcing material.
【0007】[0007]
【課題を解決するための手段】かかる課題を解決せんと
して、本発明者は鋭意研究の結果、次のような塗布型補
強材及び該補強材の施工方法を開発したものであり、そ
の要旨は以下の通りである。常温硬化二液型エポキシ塗
料であることを特徴とする、塗布型鋼板補強材。上記に
記載の塗布型鋼板補強材であって、二液型エポキシ塗料
は硬化後に可撓性を有することを特徴とする塗布型鋼板
補強材。以下に詳細に説明する。[Means for Solving the Problems] In order to solve the above problems, the present inventor has, as a result of diligent research, developed the following coating-type reinforcing material and a method of constructing the reinforcing material, the gist of which is It is as follows. A coated steel plate reinforcing material characterized by being a room temperature curing two-component epoxy paint. The coated steel sheet reinforcing material as described above, wherein the two-pack type epoxy coating has flexibility after curing. The details will be described below.
【0008】本発明に使用される鋼板補強材は、1層の
塗布材からなる、主成分はエポキシ樹脂による常温硬化
二液型塗料からなる。The steel plate reinforcing material used in the present invention is composed of a single-layer coating material, the main component of which is a room temperature curing two-component type coating material made of epoxy resin.
【0009】エポキシ樹脂は、加熱硬化後に可撓性を有
する事が必要な条件であり、これを満たすエポキシ樹
脂、硬化剤、その他の配合物を選択することが必要とな
る。加熱硬化後に可撓性を有するか否かは、複数の評価
方法が存在するが、本発明においては、JIS B 7
729に規定されたエリクセン試験機を用いてJIS
B 7777に規定されたエリクセン試験方法により測
定されるエリクセン値によって評価を行うこととした。
即ち、主剤と硬化剤その他を混合し、ドクターブレード
など適当な方法で厚さ100μmのシート状物を作成
し、180℃で30分の加熱を行った後常温迄冷却し、
上記試験方法によりエリクセン値を測定し、可撓性評価
とした。エリクセン値としては5mm以上で可撓性有
り、7mm以上で可撓性非常に有りとの評価とした。ま
ずエポキシ樹脂主剤の配合としては、ビスフェノールA
型、ビスフェノールF型等の基本的なエポキシ樹脂系
に、可撓性(付与)タイプのエポキシ樹脂を添加混合す
る、若しくは可撓性(付与)タイプのエポキシ樹脂のみを
使用するという方法が挙げられる。可撓性(付与)タイプ
のエポキシ樹脂とは、エポキシ樹脂メーカー各社から様
々なグレードで供給されているが、ダイマー酸エポキシ
樹脂、ダイマー酸変性エポキシ樹脂、ゴム変性エポキシ
樹脂、(多価)アルコールエーテル型エポキシ樹脂、ポリ
グリコール型エポキシ樹脂、ウレタン変性エポキシ樹脂
等を例示することができる。The epoxy resin is required to have flexibility after being cured by heating, and it is necessary to select an epoxy resin, a curing agent, and other compounds which satisfy the requirement. There are a plurality of evaluation methods for determining whether or not the material has flexibility after heat curing, but in the present invention, JIS B 7
JIS using the Erichsen tester specified in 729
It was decided to evaluate by the Erichsen value measured by the Erichsen test method specified in B 7777.
That is, a main agent, a curing agent, and the like are mixed, a sheet-like material having a thickness of 100 μm is prepared by an appropriate method such as a doctor blade, heated at 180 ° C. for 30 minutes, and then cooled to room temperature.
The Erichsen value was measured by the above-mentioned test method and evaluated as flexibility. The Erichsen value was evaluated to be 5 mm or more and to be flexible, and 7 mm or more to be extremely flexible. First, bisphenol A was used as the main component of the epoxy resin.
A method of adding and mixing a flexible (providing) type epoxy resin to a basic epoxy resin system such as a mold or bisphenol F type, or using only a flexible (providing) type epoxy resin. . Flexible (giving) type epoxy resin is supplied in various grades from various epoxy resin manufacturers, but dimer acid epoxy resin, dimer acid modified epoxy resin, rubber modified epoxy resin, (polyvalent) alcohol ether Type epoxy resin, polyglycol type epoxy resin, urethane modified epoxy resin and the like.
【0010】硬化剤の配合にあたっても、加熱硬化後に
可撓性を有する様に配合することが必要であるが、基本
的には従来公知のエポキシ樹脂硬化剤から選択して配合
が可能である。即ち、脂肪族アミン、芳香族アミン、酸
無水物、ユリア樹脂、メラミン樹脂、フェノール樹脂が
例示できる。脂肪族アミンとしては、ジエチレントリア
ミン(DTA)、トリエチレンテトラミン(TETA)
などや、これらの末端にアミノ基をもつ付加物が、芳香
族アミンとしては、メタフェニレンジアミン(MP
D)、ジアミノジフェニルメタン(DDM)、ジアミノ
ジフェニルスルホン(DDS)が使用できる。When the curing agent is compounded, it is necessary to compound it so that it has flexibility after heat curing, but basically it is possible to select it from conventionally known epoxy resin curing agents. That is, aliphatic amine, aromatic amine, acid anhydride, urea resin, melamine resin, and phenol resin can be exemplified. Aliphatic amines include diethylenetriamine (DTA), triethylenetetramine (TETA)
Etc., and an adduct having an amino group at these terminals is used as meta-phenylene diamine (MP
D), diaminodiphenylmethane (DDM) and diaminodiphenylsulfone (DDS) can be used.
【0011】なお、本発明になる塗布型鋼板補強材は、
塗布後、1〜2時間を経過した後、エポキシ樹脂と硬化
剤による硬化反応の進行により、塗布型鋼鈑補強材自身
が形状保持力を有することが望ましい。これは以下の理
由による。自動車製造ラインにおいて、本発明になる塗
布型補強材がプレス工程において塗布された場合、続い
て溶接工程にて鋼板が溶接され、鋼板に付着している防
錆油を取り除く湯洗工程、脱脂工程に移行するが、これ
らの工程において、湯洗に必要な水流、シャワー等が、
直接若しくは間接的に塗布された補強材にかかる場合が
ある。この時に、補強材が十分に硬化していない場合に
は、湯洗による水流やシャワーの影響で補強材が鋼板か
ら脱落したり、仮に脱落を免れても、片側の塗膜が厚く
なるなどの変形をきたす虞れがある。脱落は明らかに不
具合であるが、変形した場合にも、加熱硬化時に補強材
の塗膜が厚くなった側に大きな応力が発生し、鋼板に歪
みが生じるという不具合が発生する可能性がある。これ
らの不具合を防止するため塗布された塗布型鋼鈑補強材
自身が、加熱硬化前であっても、塗布後1〜2時間後
に、十分な形状保持力を有することにより、湯洗工程に
おける水流やシャワーに耐えうるものとなる。The coated steel plate reinforcing material according to the present invention is
It is desirable that the coating type steel plate reinforcing material itself has a shape-retaining force due to the progress of the curing reaction between the epoxy resin and the curing agent after 1 to 2 hours have passed after the coating. This is for the following reason. In an automobile manufacturing line, when the coating-type reinforcing material according to the present invention is applied in a pressing step, a steel sheet is subsequently welded in a welding step to remove rust-preventing oil adhering to the steel sheet, a dewatering step, a degreasing step However, in these steps, the water flow necessary for washing with hot water, shower, etc.
In some cases, the reinforcing material may be applied directly or indirectly. At this time, if the reinforcing material is not sufficiently hardened, the reinforcing material may fall off from the steel sheet due to the effect of water flow or shower due to hot water washing, or even if it is escaped, the coating film on one side becomes thicker. There is a risk of deformation. Although the falling-off is obviously a defect, even when it is deformed, a large stress may be generated on the side where the coating film of the reinforcing material is thickened during heat curing, and a defect may occur that the steel sheet is distorted. The coating type steel plate reinforcing material applied to prevent these problems has sufficient shape-retaining power after 1 to 2 hours after application even before heat curing, so that water flow in the hot water washing step and Can withstand a shower.
【0012】この他の配合物としては、エポキシ反応性
希釈剤がある。鋼板補強材の塗装作業性を向上させるた
めには、エポキシ樹脂塗料の粘度を低くする必要があ
り、このためにはエポキシ反応性希釈剤の配合が望まし
い。本希釈剤も各種のものが公知であり、特に限定無く
使用できる。Another formulation is an epoxy reactive diluent. In order to improve the coating workability of the steel plate reinforcing material, it is necessary to reduce the viscosity of the epoxy resin coating material, and for this purpose, the blending of an epoxy reactive diluent is desirable. Various diluents are known as the present diluent and can be used without particular limitation.
【0013】その他の配合物として、充填材、添加剤が
挙げられる。充填材としては、炭酸カルシウム、硫酸バ
リウム、タルク、クレー、カオリン、亜鉛華、酸化チタ
ン、シリカ、アルミナ等の各種の体質顔料及び着色顔料
が、又、プラスチックバルーン、ガラスバルーン、セラ
ミックバルーン、シリカバルーン、シラスバルーン等の
各種の軽量低比重充填材等が例示できる。その他添加剤
としては、脱水剤、吸湿剤、タレ防止剤、チクソトロピ
ー添加剤、分散剤、紫外線吸収剤、塗装作業性向上のた
めの高沸点溶剤、エポキシ反応性希釈剤、可塑剤、油面
接着効果増大のためのパウダーゴム、鋼板補強効果増大
のためのアクリル樹脂等が例示できる。これらの添加剤
の添加量としては、0〜10質量%が適当である。Other compounds include fillers and additives. As the filler, various extender pigments and coloring pigments such as calcium carbonate, barium sulfate, talc, clay, kaolin, zinc white, titanium oxide, silica and alumina, plastic balloons, glass balloons, ceramic balloons, silica balloons are also used. Examples include various lightweight low specific gravity fillers such as Shirasu balloon. Other additives include dehydrating agents, hygroscopic agents, anti-sagging agents, thixotropic additives, dispersants, UV absorbers, high boiling point solvents for improving coating workability, epoxy reactive diluents, plasticizers, oil surface adhesion Examples thereof include powder rubber for increasing the effect and acrylic resin for increasing the steel plate reinforcing effect. The addition amount of these additives is appropriately 0 to 10% by mass.
【0014】本発明になる塗布型補強材は、従来公知の
塗料用分散機を使用して製造することができる。即ち、
ディゾルバー、プラネタリーミキサー、オープンニーダ
ー、真空ニーダー、ロールミル、ボールミル、グレンミ
ル等の分散機である。The coating-type reinforcing material according to the present invention can be produced by using a conventionally known coating disperser. That is,
It is a disperser such as a dissolver, a planetary mixer, an open kneader, a vacuum kneader, a roll mill, a ball mill, and a Glen mill.
【0015】本発明になる補強材を必要な箇所へ塗布し
ようとすれば、エアレスポンプ等の加圧機により補強材
を圧送し、必要なサイズのノズルを使用して、従来公知
の各種塗装機により、自動車のドアパネル、クォーター
パネル、リアゲートパネル等、任意の所望箇所へ塗布さ
れる。If the reinforcing material according to the present invention is to be applied to a necessary place, the reinforcing material is pressure-fed by a pressurizing machine such as an airless pump, a nozzle of a required size is used, and various conventionally known coating machines are used. It is applied to any desired place such as a car door panel, quarter panel, rear gate panel, etc.
【0016】主剤と硬化剤との混合方法として、ますこ
の2つを予め当量比にて混合し、これを圧送し塗装機に
て塗布する方法が考えられるが、この場合には塗布作業
が連続して行われている場合には問題はないが、昼休み
や、その他何らかの理由でのラインストップがあった場
合には、配管中で硬化反応が進行し、配管を塞栓させて
しまう虞れがある。その他、主剤と硬化剤とを別々の配
管により圧送し、塗装機の直前に衝突型混合機などの従
来公知の二液混合機を配置して、当量比にて混合された
補強材を塗布する方法が例示できる。この場合には混合
機から先の部分のみの洗浄を行うことで、配管や塗装機
内の塞栓を予防できる。基本的には霧化によるスプレー
塗装ではなく、押し出し塗装の形態が望ましい。スリッ
トノズル、旋回式ノズル等の塗装装置により塗装するこ
とにより、1回の塗布により鋼板補強に必要な膜厚の補
強材が塗装できる。As a method of mixing the main agent and the curing agent, it is conceivable that the two are mixed in an equivalent ratio in advance, and the mixture is pressure-fed and applied by a coating machine. In this case, the coating operation is continuous. However, if there is a line break for lunch break or for some other reason, the curing reaction may proceed in the pipe and plug the pipe. . In addition, the main agent and the curing agent are pressure-fed by separate pipes, and a conventionally known two-liquid mixer such as a collision type mixer is arranged immediately before the coating machine to apply the reinforcing material mixed at an equivalence ratio. The method can be illustrated. In this case, it is possible to prevent embolism in the piping and the coating machine by washing only the portion ahead of the mixer. Basically, it is desirable to use extrusion coating instead of spray coating by atomization. By coating with a coating device such as a slit nozzle or a swirl type nozzle, a reinforcing material having a film thickness necessary for reinforcing a steel plate can be coated with one application.
【0017】また、配管及び塗布ノズルを30〜70℃
に加温して塗装することにより、補強材の粘性・粘度を
下げることができ、より均一かつ平滑な補強材の塗布面
を形成し、安定した品質、補強効果を得ることができ
る。30℃未満の加温であると粘性・粘度低下が十分で
はなく、70℃を超えて加温すると補強材が塗装前にゲ
ル化する虞れがある。Further, the piping and the coating nozzle are set at 30 to 70 ° C.
By heating and painting the reinforcing material, it is possible to reduce the viscosity of the reinforcing material, form a more uniform and smooth coated surface of the reinforcing material, and obtain stable quality and reinforcing effect. If the heating temperature is lower than 30 ° C, the viscosity and the viscosity are not sufficiently reduced, and if the heating temperature is higher than 70 ° C, the reinforcing material may gel before coating.
【0018】[0018]
【発明の実施の形態】本発明の理解に供するため、以下
に実施例を記載する。いうまでもなく、本発明は以下の
実施例に限定されるものではない。BEST MODE FOR CARRYING OUT THE INVENTION In order to provide an understanding of the present invention, examples will be described below. Needless to say, the present invention is not limited to the examples below.
【0019】[0019]
【実施例1】主剤として、エポキシ当量が約350のビ
スフェノールF型エポキシ樹脂100質量部、エポキシ
当量が約200のエポキシ反応性希釈剤50質量部、硬
化剤として、ジエチレントリアミン(DTA)のアミン
付加物による硬化剤50質量部、炭酸カルシウム300
質量部、添加剤30質量部をプラネタリーミキサーによ
り混合分散し、エアレスポンプにより上記主剤及び硬化
剤各々を加圧圧送し、ノズル直前に配置された混合器に
より主剤硬化剤を反応当量比にて混合し、配管及びノズ
ルを約50℃に加熱したスリットノズルにより、防錆油
の付着している0.8mm厚の自動車用鋼板に塗布膜厚
1.0mmにて塗布し、常温での硬化反応により補強材
1を得た。なお、別途測定した補強材1のエリクセン値
は7mmであり、可撓性は非常に有るとの評価であっ
た。Example 1 100 parts by mass of a bisphenol F type epoxy resin having an epoxy equivalent of about 350, 50 parts by mass of an epoxy reactive diluent having an epoxy equivalent of about 200 as a main agent, and an amine adduct of diethylenetriamine (DTA) as a curing agent. 50 parts by mass of curing agent, calcium carbonate 300
30 parts by weight of the additive and 30 parts by weight of the additive are mixed and dispersed by a planetary mixer, and the main agent and the curing agent are pressurized and pressure-fed by an airless pump, and the curing agent of the main agent is reacted at a reaction equivalent ratio by a mixer arranged immediately before the nozzle. By mixing and applying the pipe and nozzle to a slit nozzle heated to about 50 ° C to a 0.8 mm thick steel plate for automobiles with anti-rust oil applied, with a coating thickness of 1.0 mm, curing reaction at room temperature Thus, the reinforcing material 1 was obtained. The Erichsen value of the reinforcing material 1 measured separately was 7 mm, and it was evaluated that the reinforcing material 1 was extremely flexible.
【0020】[0020]
【実施例2】主剤として、エポキシ当量が約300のビ
スフェノールF型エポキシ樹脂100質量部、エポキシ
当量が約250のエポキシ反応性希釈剤50質量部、硬
化剤として、ジエチレントリアミン(DTA)のアミン
付加物による硬化剤50質量部、炭酸カルシウム300
質量部、添加剤30質量部をプラネタリーミキサーによ
り混合分散し、エアレスポンプにより上記主剤及び硬化
剤各々を加圧圧送し、ノズル直前に配置された混合器に
より主剤硬化剤を反応当量比にて混合し、配管及びノズ
ルを約50℃に加熱した旋回回転型ノズルにより、防錆
油の付着している0.8mm厚の自動車用鋼板に塗布膜
厚1.0mmにて塗布し、常温での硬化反応により補強
材2を得た。なお、別途測定した補強材2のエリクセン
値は8mmであり、可撓性は非常に有るとの評価であっ
た。Example 2 100 parts by mass of a bisphenol F type epoxy resin having an epoxy equivalent of about 300, 50 parts by mass of an epoxy reactive diluent having an epoxy equivalent of about 250 as a main agent, and an amine adduct of diethylenetriamine (DTA) as a curing agent. 50 parts by mass of curing agent, calcium carbonate 300
30 parts by weight of the additive and 30 parts by weight of the additive are mixed and dispersed by a planetary mixer, and the main agent and the curing agent are pressurized and pressure-fed by an airless pump, and the curing agent of the main agent is reacted at a reaction equivalent ratio by a mixer arranged immediately before the nozzle. By mixing and applying the pipe and nozzle to a rotating rotary nozzle heated to about 50 ° C., it is applied at a coating thickness of 1.0 mm on a 0.8 mm thick steel plate for automobiles on which rust-preventing oil is adhered, and at room temperature. The reinforcing material 2 was obtained by the curing reaction. The Erichsen value of the reinforcing material 2 measured separately was 8 mm, and it was evaluated that the reinforcing material 2 was very flexible.
【0021】[0021]
【実施例3】主剤として、エポキシ当量が約250のビ
スフェノールF型エポキシ樹脂100質量部、エポキシ
当量が約250のエポキシ反応性希釈剤50質量部、硬
化剤として、ジエチレントリアミン(DTA)のアミン
付加物による硬化剤50質量部、炭酸カルシウム300
質量部、添加剤30質量部をプラネタリーミキサーによ
り混合分散し、エアレスポンプにより上記主剤及び硬化
剤各々を加圧圧送し、ノズル直前に配置された混合器に
より主剤硬化剤を反応当量比にて混合し、配管及びノズ
ルを約50℃に加熱したスリットノズルにより、防錆油
の付着している0.8mm厚の自動車用鋼板に塗布膜厚
1.0mmにて塗布し、常温での硬化反応により補強材
3を得た。なお、別途測定した補強材3のエリクセン値
は8mmであり、可撓性は非常に有るとの評価であっ
た。Example 3 100 parts by mass of a bisphenol F type epoxy resin having an epoxy equivalent of about 250 as a main agent, 50 parts by mass of an epoxy reactive diluent having an epoxy equivalent of about 250, and an amine adduct of diethylenetriamine (DTA) as a curing agent. 50 parts by mass of curing agent, calcium carbonate 300
30 parts by weight of the additive and 30 parts by weight of the additive are mixed and dispersed by a planetary mixer, and the main agent and the curing agent are pressurized and pressure-fed by an airless pump, and the curing agent of the main agent is reacted at a reaction equivalent ratio by a mixer arranged immediately before the nozzle. By mixing and applying the pipe and nozzle to a slit nozzle heated to about 50 ° C to a 0.8 mm thick steel plate for automobiles with anti-rust oil applied, with a coating thickness of 1.0 mm, curing reaction at room temperature Thus, the reinforcing material 3 was obtained. The Erichsen value of the reinforcing material 3 measured separately was 8 mm, and it was evaluated that the reinforcing material 3 was very flexible.
【0022】[0022]
【比較例】ラクタムブロックのTDIウレタンプレポリ
マー250質量部、ポリエステルポリオールを反応当量
含有するポリウレタン樹脂100質量部、ビスフェノー
ルA型エポキシ樹脂及びジシアンジアミド潜在型硬化剤
300質量部、ガラスバルーン30質量部、炭酸カルシ
ウム200質量部、添加剤30質量部をプラネタリーミ
キサーにより混合分散し、塗布型補強材4を得た。エア
レスポンプにより塗布型補強材4を加圧圧送し、同時に
配管及びノズルを約50℃に加熱したスリットノズルに
より、防錆油の付着している0.8mm厚の自動車用鋼
板に塗布膜厚1.5mmにて塗布し補強材4を得た。な
お、別途測定した補強材4のエリクセン値は3mmであ
り、可撓性は無いとの評価であった。Comparative Example 250 parts by mass of TDI urethane prepolymer of lactam block, 100 parts by mass of polyurethane resin containing reaction equivalent of polyester polyol, 300 parts by mass of bisphenol A type epoxy resin and dicyandiamide latent curing agent, 30 parts by mass of glass balloon, carbonic acid 200 parts by mass of calcium and 30 parts by mass of additives were mixed and dispersed by a planetary mixer to obtain a coating type reinforcing material 4. The coating type reinforcing material 4 is pressure-fed by an airless pump, and at the same time, a coating thickness of 1 is applied to a 0.8 mm thick steel plate for automobiles on which rust-preventing oil is adhered by a slit nozzle in which the pipe and the nozzle are heated to about 50 ° C. It was applied at 0.5 mm to obtain a reinforcing material 4. The Erichsen value of the reinforcing material 4 measured separately was 3 mm, and it was evaluated that the reinforcing material 4 had no flexibility.
【0023】[0023]
【試験方法】(1)補強材が塗布硬化後の鋼板の外観を
観察し、歪み等の異常が無いかどうかを調べた。
(2)各試験片を、1m2あたりの質量を測定の上、補
強性を測定した。補強性は引張試験機にて測定を行っ
た。各試験片を、スパンが100mmの3点曲げタイプ
の変形測定ジグに載置し、圧縮速度5mm/分で試験片
を圧縮し、試験片が1mm変形した時の荷重を測定し、
これに重力加速度を乗じて補強性とする。[Test Method] (1) The appearance of the steel sheet after the coating and hardening of the reinforcing material was observed and examined for any abnormalities such as distortion. (2) Reinforcing properties of each test piece were measured after measuring the mass per 1 m 2 . The reinforcing property was measured by a tensile tester. Each test piece was placed on a 3-point bending type deformation measuring jig having a span of 100 mm, the test piece was compressed at a compression rate of 5 mm / min, and the load when the test piece was deformed by 1 mm was measured.
This is multiplied by the gravitational acceleration to provide reinforcement.
【0024】[0024]
【結果】(1)外観
補強材1〜補強材4とも鋼板外観に異常は見られなかっ
た。
(2)補強性(単位はNである)
[Results] (1) No abnormalities were found in the appearance of the steel sheets for the exterior reinforcement materials 1 to 4. (2) Reinforcing property (unit is N)
【0025】[0025]
【発明の効果】本発明の補強材は塗布型であるため、従
来成形物の補強材を貼着作業するために必要な条件は大
幅に緩和され、塗布ノズルを工夫することにより従来は
補強材貼着が困難若しくは不可能であった箇所にも、補
強材を塗布できるようになるため、鋼板補強の適用箇所
が大幅に増える。また、塗布作業となるため、塗布機を
自動塗装機やロボット塗装機とすることにより作業の自
動化が可能となる。また、本発明になる補強材は塗布後
1〜2時間で常温硬化するため、プレス工程にて塗布
し、化成処理工程に移行する時には塗膜が硬化している
ため、化成処理液を汚染する虞れがなく、補強材に軽量
中空充填材等を配合できるため、必要に応じて補強材の
低比重軽量化を図ることが自在に可能である。また、本
発明になる補強材の付着力は極めて強力であるため、化
成処理前の表面に防錆油が存在する自動車用鋼板にも、
容易に付着して補強材を形成することができる。また常
温での硬化反応により1〜2時間の経過時間で必要充分
な硬化による形状保持ができるため、プレス工程にて補
強材塗布後に、後工程である湯洗・脱脂工程における激
しい水流、化成処理工程を経ても補強材が形状変化、脱
落、ズレ、剥がれ等を起こす虞れはないものである。EFFECTS OF THE INVENTION Since the reinforcing material of the present invention is a coating type, the conditions required for attaching a reinforcing material of a conventional molded product can be relieved significantly. Since it becomes possible to apply the reinforcing material to the places where the attachment is difficult or impossible, the places where the steel plate reinforcement is applied are significantly increased. Further, since it is a coating work, the work can be automated by using an automatic coating machine or a robot coating machine as the coating machine. Further, since the reinforcing material according to the present invention cures at room temperature within 1 to 2 hours after application, it is applied in the pressing step, and the coating film is hardened when shifting to the chemical conversion treatment step, thus contaminating the chemical conversion treatment solution. Since there is no fear and a lightweight hollow filler or the like can be mixed with the reinforcing material, it is possible to freely reduce the specific gravity and weight of the reinforcing material as needed. Further, since the adhesive force of the reinforcing material according to the present invention is extremely strong, even for a steel sheet for automobiles in which rust preventive oil is present on the surface before chemical conversion treatment,
It can be easily attached to form a reinforcing material. In addition, since the curing reaction at room temperature can maintain the shape by necessary and sufficient curing in 1 to 2 hours elapsed time, after applying the reinforcing material in the pressing process, a strong water flow in the post-process of hot water washing / degreasing process, chemical conversion treatment. Even after the steps, the reinforcing material is not likely to change its shape, fall off, shift, peel off or the like.
───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4F100 AA08H AB03B AH03H AK53A BA02 CA02 CA23 GB32 JB13A JK06 JK17A JL00 JL02 ─────────────────────────────────────────────────── ─── Continued front page F term (reference) 4F100 AA08H AB03B AH03H AK53A BA02 CA02 CA23 GB32 JB13A JK06 JK17A JL00 JL02
Claims (2)
特徴とする、塗布型鋼板補強材1. A coating type steel plate reinforcing material, which is a room temperature curing two-component epoxy paint.
て、二液型エポキシ塗料は硬化後に可撓性を有すること
を特徴とする塗布型鋼板補強材2. The coated steel sheet reinforcing material according to claim 1, wherein the two-pack type epoxy paint has flexibility after curing.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001209604A JP2003019768A (en) | 2001-07-10 | 2001-07-10 | Coating-type steel sheet reinforcing material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001209604A JP2003019768A (en) | 2001-07-10 | 2001-07-10 | Coating-type steel sheet reinforcing material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2003019768A true JP2003019768A (en) | 2003-01-21 |
Family
ID=19045231
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001209604A Pending JP2003019768A (en) | 2001-07-10 | 2001-07-10 | Coating-type steel sheet reinforcing material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2003019768A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008081680A1 (en) | 2007-01-05 | 2008-07-10 | Nihon Tokushu Toryo Co., Ltd. | Two-package type, air-drying, vibration-damping coating composition |
| JP2009099743A (en) * | 2007-10-16 | 2009-05-07 | Kyocera Corp | Wiring board and manufacturing method thereof |
-
2001
- 2001-07-10 JP JP2001209604A patent/JP2003019768A/en active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008081680A1 (en) | 2007-01-05 | 2008-07-10 | Nihon Tokushu Toryo Co., Ltd. | Two-package type, air-drying, vibration-damping coating composition |
| JP2008163277A (en) * | 2007-01-05 | 2008-07-17 | Nippon Tokushu Toryo Co Ltd | Two-component room-temperature curing coating type vibration-damping coating composition |
| JP2009099743A (en) * | 2007-10-16 | 2009-05-07 | Kyocera Corp | Wiring board and manufacturing method thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69826017T2 (en) | FLEXIBLE MUFFLING COATING OF EPOXY RESIN | |
| US5194502A (en) | Epoxy resin, urethane-modified epoxy resin and carboxylated polyester | |
| US11820922B2 (en) | Adhesive composition | |
| JP2010139973A (en) | Method for manufacturing design model, solvent-free two-liquid quick curable urethane resin liquid for spray coating material, and solvent-free two-liquid reaction curable urethane resin putty material for mounding process | |
| TW202106506A (en) | Composite multilayer body and metal-polyolefin bonded body | |
| CA2451857C (en) | Method for coating a substrate with a sealant, sealant before and after hardening, and use of the non-hardened sealant | |
| JP5981773B2 (en) | Structural adhesive composition | |
| JP2003019768A (en) | Coating-type steel sheet reinforcing material | |
| AU750635B2 (en) | Curable sealant composition | |
| JP4004198B2 (en) | Application method of coated steel plate reinforcement | |
| CN116601256A (en) | Method for seam bonding of hem | |
| JP2003020448A (en) | Rapid curing application type reinforcing material for steel sheet and steel sheet reinforcing method | |
| JP2022095441A (en) | Pillar for vehicle body of automobile and method for manufacturing the same | |
| JPH0288684A (en) | Bonding and liquid adhesive used therefor | |
| JP2004250632A (en) | Coating-type steel sheet reinforcing material | |
| JP3849784B2 (en) | Construction method of composite steel plate reinforcement for automobiles | |
| JPH04142382A (en) | Adhesive composition | |
| JP3871576B2 (en) | Adhesive composition for automobile interior | |
| JPH01240579A (en) | Coating compound for elastomer/metal complex member, coating of said member and elastomer/metal complex member coated with said coating compound | |
| EP1186642A1 (en) | Adhesives for car bodywork construction | |
| JPH0338328A (en) | Honeycomb panel for construction | |
| JPH06299049A (en) | Coating composition for reinforcing steel sheet | |
| CN112831307B (en) | Single-component solvent-free hot melt adhesive for automobile roof, and preparation method and use method thereof | |
| KR100802812B1 (en) | High Rigidity Sheet Composition | |
| JPH02233745A (en) | Adhesive composition for hemming part of automotive body |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20050217 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20070412 |
|
| A131 | Notification of reasons for refusal |
Effective date: 20070417 Free format text: JAPANESE INTERMEDIATE CODE: A131 |
|
| A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20070606 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20070801 |