JPS627779A - Corrosion-resistant photosetting adhesive composition - Google Patents
Corrosion-resistant photosetting adhesive compositionInfo
- Publication number
- JPS627779A JPS627779A JP60147549A JP14754985A JPS627779A JP S627779 A JPS627779 A JP S627779A JP 60147549 A JP60147549 A JP 60147549A JP 14754985 A JP14754985 A JP 14754985A JP S627779 A JPS627779 A JP S627779A
- Authority
- JP
- Japan
- Prior art keywords
- adhesive composition
- acrylic
- adhesive
- corrosion
- varnish
- 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
Landscapes
- Epoxy Resins (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Optical Record Carriers And Manufacture Thereof (AREA)
Abstract
Description
【発明の詳細な説明】 産業上の利用分野 本発明は紫外線硬化性接着剤に関する。[Detailed description of the invention] Industrial applications The present invention relates to ultraviolet curable adhesives.
従来の技術
ガラスやプラスチックなどのような透明な材料を被着体
の少くとも一方に有する場合には紫外線の照射によシ硬
化する接着剤を用いることが能率的であり、このような
接着剤はよく知られている。Conventional Technology When at least one of the adherends has a transparent material such as glass or plastic, it is efficient to use an adhesive that hardens when irradiated with ultraviolet rays. is well known.
(例えば“UV、KB硬化技術n@総合技術センター発
行、557)
発明が解決しようとする問題点
このような従来の接着剤を用いた問題点として、少くと
も被着物の一部に金属が用いられている場合、特に、そ
れが蒸着によって形成されたような薄い金属層であるよ
うな場合には、接着されたものが高温多湿の条件に曝さ
れると、接着剤が腐食を促進することが多く報告されて
いる。この重大な問題に対する有効な方策はなかった。(For example, “UV, KB Curing Technology n @ Published by Sogo Technological Center, 557) Problems to be Solved by the Invention One of the problems with using such conventional adhesives is that at least part of the adherend is made of metal. If the bonded material is exposed to hot and humid conditions, the adhesive may accelerate corrosion, especially if it is a thin metal layer such as one formed by vapor deposition. There have been many reports of this, and there have been no effective measures to deal with this serious problem.
問題点を解決するだめの手段
本発明の防食性光硬化性接着剤組成物は、アクリル系光
ラジカル重合性ワニスに対し、これに溶解できるエポキ
シプレポリマーを混合したものである。Means for Solving the Problems The anticorrosive photocurable adhesive composition of the present invention is a mixture of an acrylic photoradically polymerizable varnish and an epoxy prepolymer that can be dissolved therein.
作用
すなわち、腐食性の金属、もしくは金属層を有する基材
と、透明基板との接着において、紫外線を用いて急速か
つ強固に接着させることが可能で、かつ高温多湿下でも
金属腐食が促進されない接着剤を提供することができる
。In other words, when bonding a corrosive metal or a base material with a metal layer to a transparent substrate, it is possible to bond rapidly and firmly using ultraviolet rays, and the bond does not accelerate metal corrosion even under high temperature and humidity. can provide the agent.
実施例 以下、本発明を実施例により具体的に説明する。Example Hereinafter, the present invention will be specifically explained with reference to Examples.
第1図には、表面に金属層2を有する基材1と透明基板
4とを接着剤3により接着した状態を断面図によシ説明
している。この場合、紫外線は透明基板4を透過して接
着剤3に達する。金属層2の腐食の進行形態は、透明基
板4と基材1の材質とにより異シ、これらが湿気を透過
させるような物質の場合には、全面腐食となシやすく、
水分を透過せぬ場合には端部からの水分侵入による腐食
が生じる。FIG. 1 illustrates a state in which a base material 1 having a metal layer 2 on its surface and a transparent substrate 4 are bonded together with an adhesive 3 using a cross-sectional view. In this case, the ultraviolet rays pass through the transparent substrate 4 and reach the adhesive 3. The manner in which corrosion of the metal layer 2 progresses varies depending on the materials of the transparent substrate 4 and the base material 1. If these are materials that allow moisture to pass through, full-scale corrosion is likely to occur.
If moisture is not permeable, corrosion will occur due to moisture intrusion from the edges.
実施例1
ポリエステル型多官能アクリレート(商品名:KAYA
RAD HX−820,日本化薬■製)100gに対
し、ベンジルジメチルケタールを1g溶解したアクリル
系光ラジカル重合性ワニスに対し、エポキシ当量180
〜2o○のビスフェノールA型エポキシ樹脂を5 gr
溶解させて接着剤組成物とした。該接着剤の性能を評価
するため、図に示すように金属テルル2を0.1μm厚
に蒸着した厚さ1flのメタクリル樹脂基材1と、1顧
厚の透明なメタクリル樹脂基板4とを本実施例の接着剤
組成物によシ接着させた。接着条件は、透明板4の表面
での紫外線エネルギー300mJ/fflであり接着剤
3の厚みは0.1mである。こうして作製した接着サン
プルを70°C−90%RH中に100時間放置し、変
化を観察した。結果を表に示す。Example 1 Polyester type polyfunctional acrylate (product name: KAYA
RAD HX-820, manufactured by Nippon Kayaku ■) 100g of acrylic photo-radically polymerizable varnish in which 1g of benzyl dimethyl ketal was dissolved, the epoxy equivalent was 180.
5 gr of ~2o○ bisphenol A epoxy resin
It was dissolved to form an adhesive composition. In order to evaluate the performance of the adhesive, as shown in the figure, a methacrylic resin base material 1 with a thickness of 1fl on which metallic tellurium 2 was vapor-deposited to a thickness of 0.1 μm, and a transparent methacrylic resin substrate 4 with a thickness of 1fl were prepared. Adhesion was made using the adhesive composition of the example. The bonding conditions were that the ultraviolet energy on the surface of the transparent plate 4 was 300 mJ/ffl, and the thickness of the adhesive 3 was 0.1 m. The thus prepared adhesive sample was left at 70° C. and 90% RH for 100 hours, and changes were observed. The results are shown in the table.
実施例2
ポリエステル型多官能アクリレート(商品名:KAYA
RAD HX−220,日本化薬■製)100grに
対し、塗料用アクリル樹脂(商品名:ダイヤナール B
R−64,三菱レーヨン■製)を10gr溶解し、これ
にベンジルジメチルケタールを1gr溶解した。このア
クリル系光ラジカル重合性ワニスに対し、エポキシ当量
450〜500のビスフェノールA型エポキシ樹脂を1
gr溶解して接着剤組成物とした。該接着剤組成物の
性能を評価するだめ実施例1と同一の構成・条件下で接
着サンプルを作製し、70 ’C−90%un、1o。Example 2 Polyester type polyfunctional acrylate (product name: KAYA
RAD HX-220, manufactured by Nippon Kayaku ■) 100 gr, acrylic resin for paint (product name: Dianaru B)
10g of R-64 (manufactured by Mitsubishi Rayon ■) was dissolved, and 1g of benzyl dimethyl ketal was dissolved therein. To this acrylic photoradically polymerizable varnish, 1 portion of bisphenol A epoxy resin having an epoxy equivalent of 450 to 500 was added.
gr was dissolved to obtain an adhesive composition. To evaluate the performance of the adhesive composition, an adhesive sample was prepared under the same configuration and conditions as in Example 1, and was prepared at 70'C-90% un, 1o.
時間後の変化を観察口だ。結果を表に示す。Observe the changes over time. The results are shown in the table.
実施例3
テトラヒドロフルフリルアクリレ−) 50 grとポ
リエステル型多官能アクリレート(商品名二MAID人
9日本化薬■製)sogrおよび、塗料用アクリル樹脂
ダイヤナールBR−5410grとベンジルジメチルケ
タール1grからなるアクリル系光ラジカル重合性ワニ
スに対し、側鎖型の可撓性エポキシ樹脂(商品名:’H
P−4000.旭電化工業■製)を5 gr溶解して接
着剤組成物となした。該接着剤組成物の性能を評価する
ため実施例1と同一の構成・条件で接着サンプルを作製
し、70℃−90%RH,100時間後の変化を観察し
た。結果を表に示す。Example 3 Consisting of 50 gr of tetrahydrofurfuryl acrylate), polyester type polyfunctional acrylate (trade name NiMAID Jin9 manufactured by Nippon Kayaku) sogr, acrylic resin for paint DIANAL BR-5410 gr, and benzyl dimethyl ketal 1 gr. Side chain type flexible epoxy resin (product name: 'H
P-4000. (manufactured by Asahi Denka Kogyo ■) was dissolved in an amount of 5 gr to prepare an adhesive composition. In order to evaluate the performance of the adhesive composition, adhesive samples were prepared with the same configuration and conditions as in Example 1, and changes were observed after 100 hours at 70° C. and 90% RH. The results are shown in the table.
実施例4
テトラヒドロフルフリルアクリレート50g「とポリエ
ステル型多官能アクリレ−)、(MANDA)50 g
r 、さらにジアリルフタレートプレポリマー15gr
とベンジルジメチルケタール1grからなるアクリル系
光ラジカル重合性ワニスに対し、エポキシ当量180〜
200のビスフェノールA型エポキシ樹脂5 grを溶
解して接着剤組成物とした。Example 4 50 g of tetrahydrofurfuryl acrylate (and polyester type polyfunctional acrylate), (MANDA) 50 g
r, plus 15 gr of diallyl phthalate prepolymer
For an acrylic photoradical polymerizable varnish consisting of 1gr of benzyl dimethyl ketal and
200 bisphenol A type epoxy resin was dissolved to form an adhesive composition.
接着剤接着評価のため、該接着剤を用いて、実施例1と
同一構成・条件で接着サンプルを作製し、70°C−9
0チRH,100時間後の変化を観察した。結果を表に
示す。For evaluation of adhesive adhesion, adhesive samples were prepared using the adhesive under the same configuration and conditions as in Example 1, and heated at 70°C-9.
Changes were observed after 0 hours RH and 100 hours. The results are shown in the table.
比較例1
ポリエステル多官能アクリレート(HX−220)10
0grに対し、ベンジルジメチルケタール1grを溶解
したアクリル系光ラジカル重合性ワニスを接着剤として
用い、実施例1と同一の構成・条件で接着サンプルを作
製し、これを70 ’C−90%RH中に100時間放
置して変化を観察した。結果を表に示す。Comparative Example 1 Polyester polyfunctional acrylate (HX-220) 10
Using an acrylic photoradically polymerizable varnish in which 1 gr of benzyl dimethyl ketal was dissolved in 0 gr as an adhesive, an adhesive sample was prepared with the same configuration and conditions as in Example 1, and this was heated at 70'C and 90% RH. It was left to stand for 100 hours and changes were observed. The results are shown in the table.
比較例2
金属テルルを0.1μm厚に蒸着したメタクリル樹脂基
板を70°C−90チRH中100時間放置した後の観
察結果を表に示す。Comparative Example 2 The table shows the observation results after a methacrylic resin substrate on which metallic tellurium was deposited to a thickness of 0.1 μm was left at 70° C. and 90° RH for 100 hours.
(表)70’C−90%RH,100Hr後の観察結果
発明の効果
本発明による防食性光硬化性接着剤は、高温多湿雰囲気
での金属の腐食を抑制する効果を有しており、かつ短時
間に所期の接着強度を得られるという優れた効果を有す
る。(Table) Observation results after 100 hours at 70'C - 90% RH Effects of the invention The anticorrosive photocurable adhesive according to the invention has the effect of suppressing metal corrosion in a high temperature and humid atmosphere, and It has the excellent effect of achieving the desired adhesive strength in a short period of time.
図は、金属膜を形成した基材と透明基板とを接着した状
態を説明する断面図である。
1 ・・・基材、2 ・金属層、3 接着剤、4・・
・・・・透明基板。The figure is a cross-sectional view illustrating a state in which a base material on which a metal film is formed and a transparent substrate are bonded together. 1... Base material, 2 - Metal layer, 3 Adhesive, 4...
...Transparent substrate.
Claims (3)
に可溶なエポキシプレポリマーを混合してなる防食性光
硬化性接着剤組成物。(1) An anticorrosive photocurable adhesive composition prepared by mixing an acrylic radical photopolymerizable varnish with a soluble epoxy prepolymer.
モノマーと紫外線開始触媒からなることを特徴とする特
許請求の範囲第1項記載の防食性光硬化性接着剤組成物
。(2) The anticorrosive photocurable adhesive composition according to claim 1, wherein the acrylic radical photopolymerizable varnish comprises an acrylic monomer and an ultraviolet initiation catalyst.
モノマーと高分子増粘剤および紫外線開始触媒からなる
ことを特徴とする特許請求の範囲第1項記載の防食性光
硬化性接着剤組成物。(3) The anticorrosive photocurable adhesive composition according to claim 1, wherein the acrylic radical photopolymerizable varnish comprises an acrylic monomer, a polymer thickener, and an ultraviolet initiation catalyst.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60147549A JPS627779A (en) | 1985-07-04 | 1985-07-04 | Corrosion-resistant photosetting adhesive composition |
DE8686305118T DE3669800D1 (en) | 1985-07-04 | 1986-07-01 | SIGNAL RECORDING PLATE. |
EP86305118A EP0208503B1 (en) | 1985-07-04 | 1986-07-01 | Signal recording disc |
KR1019860005380A KR900004756B1 (en) | 1985-07-04 | 1986-07-03 | Information@ recording carrier |
US07/091,349 US4760012A (en) | 1985-07-04 | 1987-08-28 | Signal recording disk |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60147549A JPS627779A (en) | 1985-07-04 | 1985-07-04 | Corrosion-resistant photosetting adhesive composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS627779A true JPS627779A (en) | 1987-01-14 |
Family
ID=15432834
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60147549A Pending JPS627779A (en) | 1985-07-04 | 1985-07-04 | Corrosion-resistant photosetting adhesive composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS627779A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5879897U (en) * | 1981-11-19 | 1983-05-30 | オリンパス光学工業株式会社 | Strobe power supply |
DE112017003978T5 (en) | 2016-08-09 | 2019-05-02 | Nidec Corporation | MOTOR UNIT |
Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5329388A (en) * | 1976-09-01 | 1978-03-18 | Showa Denko Kk | Polymerizable polymer composition |
JPS54160455A (en) * | 1978-06-08 | 1979-12-19 | Semedain Kk | Heat-curing epoxy resin composition partly curable with radiation |
JPS59159820A (en) * | 1983-03-02 | 1984-09-10 | Mitsui Toatsu Chem Inc | Ultraviolet ray-curable composition |
JPS60127321A (en) * | 1983-12-14 | 1985-07-08 | Toyobo Co Ltd | Curable resin composition of low-shrinkage potential |
JPS60243114A (en) * | 1984-05-16 | 1985-12-03 | Toyobo Co Ltd | Curable resin composition |
JPS61171721A (en) * | 1985-01-23 | 1986-08-02 | Toyobo Co Ltd | Laminate |
JPS61192724A (en) * | 1985-02-21 | 1986-08-27 | Nippon Soda Co Ltd | Photocurable composition |
JPS62516A (en) * | 1985-06-26 | 1987-01-06 | Canon Inc | Actinic energy ray-curable resin composition |
JPS624719A (en) * | 1985-07-02 | 1987-01-10 | Canon Inc | Actinic energy ray-curable resin composition |
JPS624715A (en) * | 1985-07-02 | 1987-01-10 | Canon Inc | Actinic energy ray-curable resin composition |
-
1985
- 1985-07-04 JP JP60147549A patent/JPS627779A/en active Pending
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5329388A (en) * | 1976-09-01 | 1978-03-18 | Showa Denko Kk | Polymerizable polymer composition |
JPS54160455A (en) * | 1978-06-08 | 1979-12-19 | Semedain Kk | Heat-curing epoxy resin composition partly curable with radiation |
JPS59159820A (en) * | 1983-03-02 | 1984-09-10 | Mitsui Toatsu Chem Inc | Ultraviolet ray-curable composition |
JPS60127321A (en) * | 1983-12-14 | 1985-07-08 | Toyobo Co Ltd | Curable resin composition of low-shrinkage potential |
JPS60243114A (en) * | 1984-05-16 | 1985-12-03 | Toyobo Co Ltd | Curable resin composition |
JPS61171721A (en) * | 1985-01-23 | 1986-08-02 | Toyobo Co Ltd | Laminate |
JPS61192724A (en) * | 1985-02-21 | 1986-08-27 | Nippon Soda Co Ltd | Photocurable composition |
JPS62516A (en) * | 1985-06-26 | 1987-01-06 | Canon Inc | Actinic energy ray-curable resin composition |
JPS624719A (en) * | 1985-07-02 | 1987-01-10 | Canon Inc | Actinic energy ray-curable resin composition |
JPS624715A (en) * | 1985-07-02 | 1987-01-10 | Canon Inc | Actinic energy ray-curable resin composition |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5879897U (en) * | 1981-11-19 | 1983-05-30 | オリンパス光学工業株式会社 | Strobe power supply |
DE112017003978T5 (en) | 2016-08-09 | 2019-05-02 | Nidec Corporation | MOTOR UNIT |
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