JPH024892A - Adherent material to be bonded and bonding - Google Patents
Adherent material to be bonded and bondingInfo
- Publication number
- JPH024892A JPH024892A JP15216188A JP15216188A JPH024892A JP H024892 A JPH024892 A JP H024892A JP 15216188 A JP15216188 A JP 15216188A JP 15216188 A JP15216188 A JP 15216188A JP H024892 A JPH024892 A JP H024892A
- Authority
- JP
- Japan
- Prior art keywords
- bonded
- resin
- electrophoresis
- substrate
- solution
- 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
- 239000000463 material Substances 0.000 title abstract description 10
- 230000001464 adherent effect Effects 0.000 title abstract 2
- 239000000758 substrate Substances 0.000 claims abstract description 13
- 238000001962 electrophoresis Methods 0.000 claims abstract description 12
- 239000000853 adhesive Substances 0.000 claims description 15
- 230000001070 adhesive effect Effects 0.000 claims description 15
- 239000012790 adhesive layer Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 4
- 239000004840 adhesive resin Substances 0.000 claims description 3
- 229920006223 adhesive resin Polymers 0.000 claims description 3
- 229920005989 resin Polymers 0.000 abstract description 12
- 239000011347 resin Substances 0.000 abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 7
- 125000000129 anionic group Chemical group 0.000 abstract description 3
- 125000002091 cationic group Chemical group 0.000 abstract description 3
- 229920002125 Sokalan® Polymers 0.000 abstract description 2
- 239000004584 polyacrylic acid Substances 0.000 abstract description 2
- 238000005406 washing Methods 0.000 abstract description 2
- 239000004593 Epoxy Substances 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- 239000004698 Polyethylene Substances 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 239000004814 polyurethane Substances 0.000 abstract 1
- 229920002635 polyurethane Polymers 0.000 abstract 1
- 238000000576 coating method Methods 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 2
- 229910001369 Brass Inorganic materials 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000010951 brass Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 238000005238 degreasing Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[、竜業上の利用分野]
本発明は塗装等で用いられる電気泳動膜形成法、特に微
細箇所の接着に適した接着層の形成法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for forming an electrophoretic film used in painting, etc., and particularly to a method for forming an adhesive layer suitable for adhesion in minute areas.
またこの接着層を有する接着剤およびこれを利用した接
着工法に関する。The present invention also relates to an adhesive having this adhesive layer and an adhesive method using the same.
〔従来の技術1
従来、接着層を形成する方法としては、有機溶剤系ある
いは水溶性系接着剤を吹付工法、刷毛塗り工法、ヘラ塗
り法、スプレー法、浸漬法、スピンコード法、バーコー
ド法、ロールコート法等があり又ホットメルト接着剤等
の固形接着では溶融塗工法(アプリケーター)等がある
。[Conventional technology 1] Conventionally, methods for forming adhesive layers include spraying, brush coating, spatula coating, spraying, dipping, spin-coding, and bar-coding methods using organic solvent-based or water-soluble adhesives. For solid adhesives such as hot melt adhesives, there are melt coating methods (applicator) and the like.
ところが、従来の工法では接着層が厚く、かつ均一性に
欠けるため、接着精度が悪く品質上問題があった。However, in the conventional method, the adhesive layer is thick and lacks uniformity, resulting in poor adhesion accuracy and quality problems.
特に微細箇所への接着層形成においては、接着剤のはみ
出しや塗布むら等が生じるため、微細箇所の接着に適し
た工法はなかった。In particular, when forming an adhesive layer on minute spots, there is no method suitable for adhesion on minute spots because adhesive extrusion and uneven coating occur.
本発明は上記課題を解決し、微細箇所の接着に適した工
法および接着性被着材を提供しようとするものである。The present invention aims to solve the above-mentioned problems and provide a construction method and an adhesive adherend material suitable for bonding small areas.
すなわち、本発明によれば、電着可能な接着性樹脂を含
む液中で、電気泳動法によって導電性基板上に接着層を
設けることにより接着性被着材を得、これを他の被着材
と貼り合わせる。このようにすることにより、接着剤の
はみ出しのない、均一かつ薄い接着層が得られ、高精度
かつ高品質な接着工法が実現できる。That is, according to the present invention, an adhesive adherend is obtained by providing an adhesive layer on a conductive substrate by electrophoresis in a liquid containing an adhesive resin that can be electrodeposited, and this is applied to other adherends. Attach to the material. By doing so, a uniform and thin adhesive layer without adhesive extrusion can be obtained, and a highly accurate and high quality adhesive method can be realized.
本発明において好ましく採用される電着可能な樹脂とし
て代表的なものを挙げれば、アクリル系樹脂、エポキシ
系樹脂、ポリエステル系樹脂、ポリアミド系樹脂、ポリ
ウレタン系樹脂、ポリエチレン系樹脂、ポリアクリル酸
系樹脂等で一般的に用いられる樹脂をベースとしたもの
である。Representative examples of electrodepositable resins preferably employed in the present invention include acrylic resins, epoxy resins, polyester resins, polyamide resins, polyurethane resins, polyethylene resins, and polyacrylic acid resins. It is based on a resin commonly used in, etc.
電気泳動法としては、前記樹脂を脱塩水で1〜50%に
希釈したものを電気泳動液とし、この液中で基板を対極
にたいしてアニオン系では正極に、カチオン系では負極
におき、直流電源を用いて印加電圧と時間を調節するこ
とにより所望の接着M厚を設ける。In the electrophoresis method, the above-mentioned resin is diluted to 1 to 50% with demineralized water as an electrophoresis solution, and the substrate is placed in this solution as the positive electrode for anionic systems and the negative electrode for cationic systems, and a DC power source is turned on. A desired adhesive M thickness is provided by adjusting the applied voltage and time.
通常は印加電圧20〜200V、電流密度05〜3A/
dm” 、処理時間10〜1808eCで、1〜30μ
mの好ましい厚さの接着層が得られる。Usually applied voltage is 20-200V, current density is 05-3A/
dm”, processing time 10-1808eC, 1-30μ
An adhesive layer of a preferred thickness of m is obtained.
電気泳動液のpHは、アニオン系では80〜10、 O
,カチオン系では4〜7、浴温は15〜30℃が適当で
ある。The pH of the electrophoresis solution is 80-10 for anionic systems, O
, 4 to 7 for cationic systems, and a suitable bath temperature of 15 to 30°C.
次いで水洗後約50〜60℃で5分程度予備乾燥し、そ
の後別の被着材を所定の位置に貼り合せ再度80〜20
0℃の乾燥炉にて10〜30分程度加程度、完全接着し
完成する。Next, after washing with water, pre-dry it at about 50-60°C for about 5 minutes, then paste another adherend in place and dry it again at 80-20°C.
Complete adhesion is completed in a drying oven at 0°C for about 10 to 30 minutes.
以上により高信頼性、高品質の接着工法が可能である。As a result of the above, a highly reliable and high quality adhesive method is possible.
〔実施例]
以下に実施例を示し、本発明をさらに詳しく説明するが
、本発明は本実施例のみに限定されるものではない。[Example] The present invention will be explained in more detail with reference to Examples below, but the present invention is not limited to these Examples.
実施例1
電気泳動液として、ポリエステル系樹脂(大日本インキ
化学社製) FINETEX ES−525: 60部
FrNETEX525 : 40部を混合し、次いで架
橋剤/触媒(大日本インキ化学社製) PERMAST
AT CR−5/ CatPA−20を5:2.5の割
合で前記樹脂中に添加し、マグネチックスターラにて7
時間分散し、脱塩水を用いて樹脂分として15%に希釈
したものを用いた。Example 1 As an electrophoresis liquid, 60 parts of polyester resin (manufactured by Dainippon Ink Chemical Co., Ltd.) FINETEX ES-525 and 40 parts of FrNETEX525 were mixed, and then crosslinking agent/catalyst (manufactured by Dainippon Ink Chemical Co., Ltd.) PERMAST
AT CR-5/CatPA-20 was added to the resin at a ratio of 5:2.5 and stirred with a magnetic stirrer for 7
The resin was dispersed over time and diluted to 15% as a resin content using demineralized water.
基板としては、黄銅材+00x 50X O,ltmm
の大きさのものを用い、トリエタン脱脂、アルカリクリ
ーナ脱脂等通常の前処理を行った。The board is brass material +00x 50X O, ltmm
A sample of this size was used and subjected to conventional pretreatments such as triethane degreasing and alkali cleaner degreasing.
この基板を正極に、対橋にステンレス板を用い、浴温2
0〜25℃、電圧50vにて1分間電気泳動処理をし、
2μmの接着層を基板上に形成した。This substrate was used as the positive electrode, a stainless steel plate was used as the opposite bridge, and the bath temperature was 2.
Electrophoresis was performed for 1 minute at 0 to 25°C and a voltage of 50 V.
A 2 μm adhesive layer was formed on the substrate.
これをオーブンにて50℃5分間予備加熱し、次いでこ
の基板と、接着層が形成されていない別の基板とを貼り
合わせ、 150℃lO分間加熱して接着を完了した。This was preheated in an oven at 50° C. for 5 minutes, and then this substrate and another substrate on which no adhesive layer was formed were bonded together, and the bonding was completed by heating at 150° C. for 10 minutes.
この例の剥離強度は、3〜5 kg/Cmであり、良好
な接着が実現できた。The peel strength of this example was 3 to 5 kg/Cm, and good adhesion was achieved.
実施例2
電気泳動液として、ポリエステル系樹脂(犬日本インキ
化学社製) FINETEX ES−525+ 70部
。Example 2 As an electrophoresis liquid, 70 parts of polyester resin (manufactured by Inu Nippon Ink Chemical Co., Ltd.) FINETEX ES-525+ was used.
FINETEX ES−675: 30部を混合し、次
イテ架橋剤/触媒(大日本インキ化学社製) BECK
AMINE PM−N/Cat ES−2を6=3の割
合で前記樹脂中に添加し、マグネチックスターにて7時
間分散し、脱塩水を用い樹脂分として20%に希釈した
ものを用いた。FINETEX ES-675: Mix 30 parts and add the following crosslinking agent/catalyst (manufactured by Dainippon Ink Chemical Co., Ltd.) BECK
AMINE PM-N/Cat ES-2 was added to the resin at a ratio of 6=3, dispersed for 7 hours using a magnetic star, and diluted to 20% resin content using demineralized water.
基板としては、黄銅材100x 50x O,ltmm
の大きさのものにトリエタン脱脂、アルカリクリーナ脱
脂、次いでアルカリ電解脱脂し、水洗後、ニッケルメッ
キ5μmを施したものを用いた。As a board, brass material 100x 50x O, ltmm
The size of the sample was degreased with triethane, degreased with alkali cleaner, then alkaline electrolytically degreased, washed with water, and then plated with 5 μm of nickel.
この基板を正極に、対極にステンレス板を用い、浴温2
0〜25℃、電圧120■にて1分間電気泳動処理をし
、10μmの接着層を基板上に形成した。Using this substrate as the positive electrode and a stainless steel plate as the counter electrode, the bath temperature was 2.
Electrophoresis was performed for 1 minute at 0 to 25° C. and a voltage of 120 μm to form a 10 μm adhesive layer on the substrate.
これを50℃で5分間予備加熱し、次いでこの基板と、
接着層が形成されていない別の基板とを貼り合わせ、
100℃で20分間加熱して接着を完了した。This was preheated at 50°C for 5 minutes, and then this substrate and
Attach it to another substrate that does not have an adhesive layer,
Adhesion was completed by heating at 100° C. for 20 minutes.
この例の剥離強度は、4〜6 kg/cmであり、良好
な接着が実現できた。The peel strength of this example was 4 to 6 kg/cm, and good adhesion was achieved.
[発明の効果]
以上説明したように、本発明によって、均一かつ薄い接
着層を有する接着性被着材が得られ、高精度かつ高品質
の接着工法が実現できた。[Effects of the Invention] As explained above, according to the present invention, an adhesive adherend having a uniform and thin adhesive layer can be obtained, and a highly accurate and high quality adhesive method can be realized.
特許出願人 キャノン株式会社 代 理 人 弁理士 苦杯 忠Patent applicant: Canon Co., Ltd. Representative Patent Attorney Tadashi Kukai
Claims (1)
接着層を有することを特徴とする接着性被着材。 2)導電性基板上に電着可能な接着性樹脂を含む液中で
、電気泳動を行うことを特徴とする接着工法。[Scope of Claims] 1) An adhesive adherend comprising an adhesive layer made of an adhesive resin and formed by electrophoresis. 2) An adhesive method characterized by performing electrophoresis in a liquid containing an adhesive resin that can be electrodeposited onto a conductive substrate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15216188A JPH024892A (en) | 1988-06-22 | 1988-06-22 | Adherent material to be bonded and bonding |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15216188A JPH024892A (en) | 1988-06-22 | 1988-06-22 | Adherent material to be bonded and bonding |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH024892A true JPH024892A (en) | 1990-01-09 |
Family
ID=15534357
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15216188A Pending JPH024892A (en) | 1988-06-22 | 1988-06-22 | Adherent material to be bonded and bonding |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH024892A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6588095B2 (en) * | 2001-04-27 | 2003-07-08 | Hewlett-Packard Development Company, Lp. | Method of processing a device by electrophoresis coating |
-
1988
- 1988-06-22 JP JP15216188A patent/JPH024892A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6588095B2 (en) * | 2001-04-27 | 2003-07-08 | Hewlett-Packard Development Company, Lp. | Method of processing a device by electrophoresis coating |
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