JPH0116873B2 - - Google Patents
Info
- Publication number
- JPH0116873B2 JPH0116873B2 JP6575980A JP6575980A JPH0116873B2 JP H0116873 B2 JPH0116873 B2 JP H0116873B2 JP 6575980 A JP6575980 A JP 6575980A JP 6575980 A JP6575980 A JP 6575980A JP H0116873 B2 JPH0116873 B2 JP H0116873B2
- Authority
- JP
- Japan
- Prior art keywords
- adhesive
- parts
- synthetic resin
- contact cement
- resin foams
- 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.)
- Expired
Links
- 239000006260 foam Substances 0.000 claims description 27
- 230000001070 adhesive effect Effects 0.000 claims description 24
- 239000000853 adhesive Substances 0.000 claims description 23
- 239000004568 cement Substances 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 239000012790 adhesive layer Substances 0.000 claims description 9
- 229920000103 Expandable microsphere Polymers 0.000 claims description 7
- 229920003002 synthetic resin Polymers 0.000 claims description 7
- 239000000057 synthetic resin Substances 0.000 claims description 7
- 238000005187 foaming Methods 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims 1
- 239000004005 microsphere Substances 0.000 description 7
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 6
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- 239000003094 microcapsule Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
ウレタン樹脂発泡体、スチレン樹脂発泡体、塩
化ビニル樹脂発泡体、ポリプロピレン樹脂発泡
体、ポリビニルアセタール発泡体などの合成樹脂
発泡体同士、またはこのような発泡体と他の柔軟
な素材とを貼合わせて椅子、ソフア、ベツド、マ
ツトその他の柔軟性蘂地材として用いる場合、従
来有機溶剤型コンタクトセメントが用いられて来
た。しかるに近年大気汚染、労働環境衛生、火災
などの面から有機溶剤型コンタクトセメントに代
つて、無害で安全な水性コンタクトセメントが普
及しつつある。しかるに前述のような発泡体の接
着に水性コンタクトセメントを使用すると、接着
剤液が発泡体の孔内へ浸入して固化するため、接
着層付近を中心として発泡体の柔軟性が失われて
しまうという重大な欠点があつた。
本発明は上記のような欠点を有しない発泡体用
接着剤組成物および該接着剤組成物を使用する発
泡体の接着方法に関する。
本発明組成物は、水性コンタクトセメント100
部に対し、発泡性マイクロスフエアー2ないし10
部を混合してなるものである。この接着剤組成物
を、接着しようとする発泡体同士、または発泡体
と他の柔軟な素材の両方の接着面に塗布し、接着
剤層を加熱して水分を乾燥させると同時に発泡さ
せ、その後両方をコンタクトして着すれば、接着
層付近の柔軟性を失うことなく強力に接着するこ
とができる。
本発明で使用する水性コンタクトセメントと
は、クロロプレンゴム、アクリロニトリル・ブタ
ジエンゴム、スチレン・ブタジエンゴム、アクリ
ルゴムなどの自着性ある樹脂の水性ラテツクスを
意味し、また発泡性マイクロスフエアーとは、例
えば特許第518820号に記載の塩化ビニリデン共重
合樹脂などの熱可塑性合成樹脂のマイクロカプセ
ル中に、低沸点ガス状物を含んだもので、加熱す
ると包含されているガス状物が気化膨張し、樹脂
マイクロカプセルを膨張させて著しく体積が増大
する性質を持つたものを指す。
本発明において、水性コンタクトセメントと発
泡性マイクロスフエアーの混合比は、水性コンタ
クトセメント100部に対し、マイクロスフエアー
2ないし10部であることが必要である。マイクロ
スフエアーの混合比が前記範囲未満であると、接
着層の発泡性にむらを生じ、満足な柔軟性が得ら
れない。またマイクロスフエアーの混合比が前記
範囲をこえると、接着剤のコンタクト性が失わ
れ、接着力が著しく低下する。
以下実施例により、本発明をさらに詳細に説明
する。実施例中部とあるは、重量による。
実施例 1
水性コンタクトセメント(パネルマスター140
〜8003,カネボウエヌエスシー社製)100部に対
し、発泡性マイクロスフエアー2ないし10部を表
―1に示すように混入し、接着剤組成物を作つ
た。
厚み3mmの発泡ウレタンシートと、70μ軟質塩
ビレザーのそれぞれの接着すべき面に、上記接着
剤組成物をスプレーガンで塗布量100g/m2の割
合で塗布し、80℃で2分間乾燥したところ、接着
剤層の水分が飛び、発泡した。次に3mm発泡ウレ
タンシートと塩ビシートとを互いに定位置に持ち
来たり、貼合わせ、ハンドロールで圧締して接着
を完了した。この接着物について柔軟性及び80℃
ピール性を測定した。比較のため、水性コンタク
トセメントのみを用いたもの、水性コンタクトセ
メント100部に対し、マイクロスフエアー1部、
15部および20部を混合したものを用いて同様に試
験した。
By laminating synthetic resin foams such as urethane resin foam, styrene resin foam, vinyl chloride resin foam, polypropylene resin foam, and polyvinyl acetal foam, or by laminating such foams with other flexible materials. Conventionally, organic solvent-based contact cement has been used as flexible foot material for chairs, sofas, beds, mats, and other items. However, in recent years, water-based contact cement, which is harmless and safe, has become popular in place of organic solvent-based contact cement due to concerns about air pollution, occupational health, and fire. However, when water-based contact cement is used to bond foams as described above, the adhesive liquid penetrates into the pores of the foam and solidifies, causing the foam to lose its flexibility mainly near the adhesive layer. There was a serious drawback. The present invention relates to an adhesive composition for foams that does not have the above-mentioned drawbacks and a method for bonding foams using the adhesive composition. The composition of the present invention contains water-based contact cement 100%
2 to 10 foamed microspheres per part
It is made by mixing parts. This adhesive composition is applied to the bonding surfaces of the foams to be bonded together or to both the foam and other flexible materials, and the adhesive layer is heated to dry moisture and foam at the same time, and then If both are attached in contact with each other, strong adhesion can be achieved without losing flexibility near the adhesive layer. The aqueous contact cement used in the present invention refers to an aqueous latex of self-adhesive resin such as chloroprene rubber, acrylonitrile-butadiene rubber, styrene-butadiene rubber, and acrylic rubber, and the term "expandable microspheres" refers to, for example, Microcapsules of thermoplastic synthetic resin such as vinylidene chloride copolymer resin described in Patent No. 518820 contain low-boiling gaseous substances. When heated, the contained gaseous substances vaporize and expand, causing the resin to evaporate and expand. Refers to microcapsules that have the property of expanding significantly to increase their volume. In the present invention, the mixing ratio of aqueous contact cement and expandable microspheres is required to be 2 to 10 parts of microspheres to 100 parts of aqueous contact cement. If the mixing ratio of the microspheres is less than the above range, the foamability of the adhesive layer will be uneven and satisfactory flexibility will not be obtained. Furthermore, if the mixing ratio of the microspheres exceeds the above range, the contact properties of the adhesive will be lost and the adhesive strength will be significantly reduced. The present invention will be explained in more detail with reference to Examples below. "Middle part" in the example is based on weight. Example 1 Water-based contact cement (Panel Master 140
~8003, manufactured by Kanebo NSC) and 2 to 10 parts of expandable microspheres were mixed as shown in Table 1 to prepare an adhesive composition. The above adhesive composition was applied with a spray gun at a coating amount of 100 g/m 2 to the surfaces to be bonded of a 3 mm thick urethane foam sheet and 70 μ soft PVC leather, and dried at 80°C for 2 minutes. , moisture in the adhesive layer evaporated and foaming occurred. Next, the 3 mm foamed urethane sheet and the PVC sheet were brought into position and pasted together, and the adhesive was completed by pressing with a hand roll. Flexibility and 80℃ for this adhesive
Peelability was measured. For comparison, one using only water-based contact cement, 1 part of microsphere for 100 parts of water-based contact cement,
A similar test was conducted using a mixture of 15 parts and 20 parts.
【表】【table】
【表】
表1からわかるように、発泡性マイクロスフエ
アーの添加量が少なすぎると発泡性にむらを生
じ、発泡しなかつたところは接着剤のために硬く
なり、柔軟性が損われた。発泡性マイクロスフエ
アーが過剰になると、発泡が著しく、接着剤自身
の強度がなくなつてしまうことが比較例―3でわ
かる。発泡性マイクロスフエアーが水性コンタク
トセメント100部に対し10部以上になると、接着
性そのものが失われ、塩ビレザーへの接着が著し
く低くなることが比較例―4からわかる。
実施例 2
水性コンタクトセメント(パネルマスター140
―8000、カネボウエヌエスシー社製)100部に対
し、発泡性マイクロスフエアー3部を入れた接着
剤組成物を作つた。
厚み3mmの発泡ウレタンシートと厚み10mmの発
泡ウレタンシートのそれぞれ接着すべき面に、上
記接着剤組成物をスプレーガンで表―2に示すご
とき20―100g/m2の割合で塗布し、100℃で2分
乾燥して水分を飛ばし接着層を発泡させた。次い
で3mm発泡ウレタンシートと10mm発泡ウレタンシ
ートを貼合わせ、ハンドロールで強く押え圧着し
接着を完了した。この接着物の接着強度と柔軟性
を観測した。比較のため水性コンタクトセメント
のみを用いた時の同性能を示した。[Table] As can be seen from Table 1, when the amount of foamable microspheres added was too small, the foaming property became uneven, and the areas where foaming did not occur became hard due to the adhesive and the flexibility was impaired. Comparative Example 3 shows that when the amount of foamable microspheres becomes excessive, foaming occurs significantly and the adhesive itself loses its strength. Comparative Example 4 shows that when the amount of expandable microspheres is 10 parts or more per 100 parts of water-based contact cement, the adhesive property itself is lost and the adhesion to PVC leather becomes significantly lower. Example 2 Water-based contact cement (Panel Master 140
An adhesive composition was prepared by adding 3 parts of expandable microspheres to 100 parts of 8000 (manufactured by Kanebo NSC). The above adhesive composition was applied with a spray gun at a rate of 20 to 100 g/m 2 as shown in Table 2 to the surfaces to be bonded of a 3 mm thick urethane foam sheet and a 10 mm thick urethane foam sheet, respectively, and heated at 100°C. The adhesive layer was dried for 2 minutes to remove moisture and foam the adhesive layer. Next, the 3 mm foamed urethane sheet and the 10mm foamed urethane sheet were pasted together, and the adhesive was completed by pressing firmly with a hand roll. The adhesive strength and flexibility of this adhesive were observed. For comparison, the same performance was shown when only water-based contact cement was used.
【表】【table】
【表】
表―2で判るように、本発明例では少量の塗布
量でも、接着剤が発泡し、発泡体の孔から突出す
るため十分な接着を得ることが出来るが、水性コ
ンタクトセメントのみでは少量塗布では接着剤が
発泡体の孔に流れ込んで均一な接着層を形成しな
いため接着力は低下する。塗布量を多くすると接
着性は加善されるが柔軟性が失われてしまう。[Table] As can be seen from Table 2, in the example of the present invention, even with a small amount of application, sufficient adhesion can be obtained because the adhesive foams and protrudes from the pores of the foam, but with only aqueous contact cement. If a small amount is applied, the adhesive will flow into the pores of the foam and will not form a uniform adhesive layer, resulting in a decrease in adhesive strength. If the coating amount is increased, adhesion will be improved, but flexibility will be lost.
Claims (1)
泡の発泡性マイクロスフエアー2ないし10部を混
合してなる合成樹脂発泡体同士または合成樹脂発
泡体と他の柔軟な被着材とを接着するために使用
する接着剤組成物。 2 合成樹脂発泡体同士または合成樹脂発泡体と
他の柔軟な被着材とを接着するに際し、水性コン
タクトセメント100部に対し、未発泡の発泡性マ
イクロスフエアー2ないし10部を混合してなる接
着剤組成物を両方の接着面に塗布し、接着剤層を
加熱して水分を乾燥させると同時に発泡させ、そ
の後両者をコンタクトして接着することを特徴と
する合成樹脂発泡体の接着方法。[Claims] 1. Synthetic resin foams made by mixing 2 to 10 parts of unfoamed expandable microspheres to 100 parts of aqueous contact cement, or synthetic resin foams and other flexible adherends. Adhesive composition used for bonding. 2. When adhering synthetic resin foams to each other or synthetic resin foams to other flexible adherends, it is made by mixing 2 to 10 parts of unfoamed expandable microspheres to 100 parts of water-based contact cement. A method for adhering synthetic resin foams, which comprises applying an adhesive composition to both adhesive surfaces, heating the adhesive layer to dry water and foaming at the same time, and then contacting and adhering the two.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6575980A JPS56161483A (en) | 1980-05-16 | 1980-05-16 | Adhesive composition for foam and bonding method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6575980A JPS56161483A (en) | 1980-05-16 | 1980-05-16 | Adhesive composition for foam and bonding method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56161483A JPS56161483A (en) | 1981-12-11 |
| JPH0116873B2 true JPH0116873B2 (en) | 1989-03-28 |
Family
ID=13296271
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6575980A Granted JPS56161483A (en) | 1980-05-16 | 1980-05-16 | Adhesive composition for foam and bonding method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS56161483A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003011994A1 (en) * | 2001-07-27 | 2003-02-13 | National Starch And Chemical Investment Holding Coporation | Foamed emulsion adhesive |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19607387A1 (en) * | 1996-02-28 | 1997-01-02 | Henkel Kgaa | Aq. filled adhesive based on rubbery polymer with low emission and shrinkage |
| JP4886259B2 (en) * | 2005-09-27 | 2012-02-29 | 積水化学工業株式会社 | Water-based adhesive |
-
1980
- 1980-05-16 JP JP6575980A patent/JPS56161483A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003011994A1 (en) * | 2001-07-27 | 2003-02-13 | National Starch And Chemical Investment Holding Coporation | Foamed emulsion adhesive |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56161483A (en) | 1981-12-11 |
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