JPH0688380B2 - Ethylene / propylene rubber composite and method for producing the same - Google Patents
Ethylene / propylene rubber composite and method for producing the sameInfo
- Publication number
- JPH0688380B2 JPH0688380B2 JP25616489A JP25616489A JPH0688380B2 JP H0688380 B2 JPH0688380 B2 JP H0688380B2 JP 25616489 A JP25616489 A JP 25616489A JP 25616489 A JP25616489 A JP 25616489A JP H0688380 B2 JPH0688380 B2 JP H0688380B2
- Authority
- JP
- Japan
- Prior art keywords
- adhesive
- ethylene
- rubber
- heat
- rubber composite
- 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 - Lifetime
Links
- 229920001971 elastomer Polymers 0.000 title claims description 54
- 239000005060 rubber Substances 0.000 title claims description 53
- 239000002131 composite material Substances 0.000 title claims description 14
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 title claims 2
- 239000000853 adhesive Substances 0.000 claims description 50
- 230000001070 adhesive effect Effects 0.000 claims description 50
- 239000000463 material Substances 0.000 claims description 41
- 229920001577 copolymer Polymers 0.000 claims description 8
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 8
- -1 acid-modified ethylene compound Chemical class 0.000 claims description 7
- 239000012790 adhesive layer Substances 0.000 claims description 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical class C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 4
- 239000004743 Polypropylene Substances 0.000 claims description 4
- 229920006226 ethylene-acrylic acid Polymers 0.000 claims description 4
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 claims description 4
- 239000005042 ethylene-ethyl acrylate Substances 0.000 claims description 4
- 229920000098 polyolefin Polymers 0.000 claims description 4
- 229920003051 synthetic elastomer Polymers 0.000 claims description 4
- 239000005061 synthetic rubber Substances 0.000 claims description 4
- 239000004925 Acrylic resin Substances 0.000 claims description 3
- 229920000178 Acrylic resin Polymers 0.000 claims description 3
- QLZJUIZVJLSNDD-UHFFFAOYSA-N 2-(2-methylidenebutanoyloxy)ethyl 2-methylidenebutanoate Chemical compound CCC(=C)C(=O)OCCOC(=O)C(=C)CC QLZJUIZVJLSNDD-UHFFFAOYSA-N 0.000 claims description 2
- QHZOMAXECYYXGP-UHFFFAOYSA-N ethene;prop-2-enoic acid Chemical compound C=C.OC(=O)C=C QHZOMAXECYYXGP-UHFFFAOYSA-N 0.000 claims description 2
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 claims description 2
- 229920000573 polyethylene Polymers 0.000 claims description 2
- 229920001155 polypropylene Polymers 0.000 claims description 2
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000004636 vulcanized rubber Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical group C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- 229920002943 EPDM rubber Polymers 0.000 description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- 239000006244 Medium Thermal Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920006225 ethylene-methyl acrylate Polymers 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 2
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000004716 Ethylene/acrylic acid copolymer Substances 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 239000006242 Semi-Reinforcing Furnace Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 230000036772 blood pressure Effects 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- LUZSPGQEISANPO-UHFFFAOYSA-N butyltin Chemical compound CCCC[Sn] LUZSPGQEISANPO-UHFFFAOYSA-N 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000013016 damping Methods 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 229920003244 diene elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- ZMHZSHHZIKJFIR-UHFFFAOYSA-N octyltin Chemical compound CCCCCCCC[Sn] ZMHZSHHZIKJFIR-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、耐候性の優れたEP系ゴム成形品の片面又は両
面に粘着材を接着してなる簡易取り付け可能なEP系ゴム
複合体及びその製造方法に関し、該EP系ゴム複合体は緩
衝材,防振材,防音材等として電機製品等の分野に広く
利用することができる。DETAILED DESCRIPTION OF THE INVENTION [Industrial field of application] The present invention relates to a EP rubber composite that is easily attachable and is formed by adhering an adhesive on one or both sides of an EP rubber molded article having excellent weather resistance. Regarding the manufacturing method, the EP rubber composite can be widely used as a cushioning material, a vibration-proof material, a sound-proof material, etc. in the field of electrical products and the like.
ラジオ,ステレオ,パーソナルコンピュータ等の電気機
器や高精度測定を要する計測機器には、これらの機器を
振動や衝撃から保護する目的でその所要箇所に緩衝材や
防振材さらには防音材が取付けられている。こうした緩
衝材等としては従来天然ゴムや合成ゴムからなる成形品
が使用されており、該緩衝材は、上記機器等の底面に凹
みを設けてその凹みに嵌め込んだりあるいはこれら緩衝
材シートの片面に離形紙付き粘着材を接着することによ
って取付けられる。又電卓や血圧計等の機器には、すべ
り止めや衝突のショックを和らげる目的で防音・防振材
が取付けられており、その適用形態は上記とほぼ同じで
ある。For electrical equipment such as radios, stereos, personal computers, and other measurement equipment that requires high-accuracy measurement, cushioning materials, vibration-proof materials, and sound-proof materials are installed at the required locations in order to protect these equipment from vibration and shock. ing. As such a cushioning material or the like, a molded product made of natural rubber or synthetic rubber has been conventionally used, and the cushioning material is provided with a recess on the bottom surface of the above-mentioned equipment and fitted into the recess, or one side of these cushioning material sheets. It is attached by adhering an adhesive material with release paper to. Further, a device such as a calculator or a blood pressure monitor is provided with a soundproofing / vibrating material for the purpose of preventing slippage and shock of a collision, and its application form is almost the same as the above.
ところで緩衝材として従来から使用されてきた天然ゴム
や殆んどの合成ゴムは、耐候性に問題があり、長期間、
空気中に放置しておくと表面にクラックが生じたり、硬
度が高くなって可撓性を失うという事態が発生する。こ
れに対し合成ゴムのなかでもEP系ゴムは例外的に耐候性
が優れ、その意味では緩衝材としての長期使用に耐え得
るものである。しかしながらEP系ゴムは耐候性が良好で
ある反面、他のゴム系材料と比べて接着性が悪く、離形
紙付き粘着材を該EP系ゴム成形品に接着しようとしても
充分に接着することができないという問題点があった。
即ちEP系ゴム製の緩衝材においては、簡易取付け可能な
離形紙付き粘着材を有する緩衝材や防振材の製造が困難
であり、耐候性の優れたEP系ゴム成形品の適用を阻害す
る要因となっていた。By the way, natural rubber and most synthetic rubbers that have been conventionally used as cushioning materials have a problem in weather resistance,
If left in the air, cracks may occur on the surface, or the hardness may increase and the flexibility may be lost. On the other hand, among synthetic rubbers, EP rubber is exceptionally excellent in weather resistance, and in that sense, it can withstand long-term use as a cushioning material. However, while EP rubber has good weather resistance, it has poor adhesion compared to other rubber materials, and even if an adhesive material with release paper is attempted to adhere to the EP rubber molded product, it can be sufficiently adhered. There was a problem that it could not be done.
In other words, in the case of EP-based rubber cushioning materials, it is difficult to manufacture cushioning materials and vibration-proof materials that have an adhesive material with release paper that can be easily attached, and this hinders the application of EP-based rubber molded products with excellent weather resistance. Had become a factor to.
本発明は、こうした事情に着目してなされたものであっ
て、EP系ゴムの難接着性を克服することによりEP系ゴム
の長所を生かそうとするものであって、(離形紙付き)
粘着材を強固に接着した、簡易取付け可能なEP系ゴム複
合体(緩衝材、防振材又は防音材)を提供しようとする
ものである。The present invention has been made in view of these circumstances, and aims to utilize the advantages of EP rubber by overcoming the poor adhesion of EP rubber (with release paper).
It is intended to provide an EP-based rubber composite (a cushioning material, a vibration-proof material or a sound-proof material) in which an adhesive material is firmly adhered and which can be easily attached.
上記目的を達成した本発明のEP系ゴム複合体は、EP系ゴ
ム成形品の少なくとも一面に熱活性形接着剤層を解して
粘着材を接着してなる点に要旨を有するものであり、又
上記EP系ゴム複合体を得る本発明方法は、熱活性形接着
剤を、EP系ゴム成形品と粘着材の間に介装し、加熱圧締
して接合一体化する点に要旨が存在する。The EP-based rubber composite of the present invention which has achieved the above-mentioned object has a gist in that the heat-activatable adhesive layer is unwound on at least one surface of the EP-based rubber molded article to bond an adhesive material, Further, the method of the present invention for obtaining the above EP rubber composite has a gist in that a heat-activatable adhesive is interposed between an EP rubber molded article and an adhesive material and heat-pressed to integrally bond them. To do.
本発明においてEP系ゴムとしては、EPM(エチレン・プ
ロピレンゴム(Ethylene Propylene Rubber))、EPDM
(エチレン・プロピレン・ジエンゴム(Ethylene Propy
lene Diene Rubber)等を挙げることができ、これらは
加硫剤を加えて熱架橋させるのが一般的であり、本発明
におけるEP系ゴムは加硫ゴムに限定される。これらEP系
ゴムは、前記した通り耐候性に優れているものの接着性
殊に粘着剤との接着性が悪いという問題点がある。In the present invention, EP rubbers include EPM (Ethylene Propylene Rubber), EPDM
(Ethylene Propylene Diene Rubber
Lene Diene Rubber) and the like, which are generally added with a vulcanizing agent and thermally crosslinked, and the EP rubber in the present invention is limited to vulcanized rubber. Although these EP rubbers have excellent weather resistance as described above, they have a problem in that they have poor adhesiveness, particularly adhesiveness with a pressure-sensitive adhesive.
本発明は、こうしたEP系ゴムの欠点を解消すべく、EP系
ゴムと粘着剤を接着剤層を介して強固に接合しようと考
え種々検討を重ねた結果、完成されたものである。The present invention has been completed as a result of various studies in order to firmly bond the EP rubber and the pressure-sensitive adhesive via the adhesive layer in order to eliminate the drawbacks of the EP rubber.
即ち本発明における接着剤は、EP系ゴムと粘着剤の双方
に類似した分子構造を有する化合物を主成分とする組成
物であり、該接着剤はその分子構造に起因してEP系ゴム
と粘着剤の双方に対して親和性を示すので表面の微細な
空隙までよく浸透して投錨効果を発揮し、優れた接着性
を発現する。特に難接着性であるEP系ゴムに対して効果
的に作用し、その欠点を克服するものであり、EP系ゴム
と粘着材を強固に一体化することができる。That is, the adhesive in the present invention is a composition whose main component is a compound having a molecular structure similar to both the EP rubber and the pressure-sensitive adhesive, and the adhesive adheres to the EP rubber due to its molecular structure. Since it has an affinity for both agents, it penetrates well even into minute voids on the surface and exerts an anchoring effect, and exhibits excellent adhesiveness. In particular, it works effectively against EP rubber that is difficult to adhere to and overcomes its drawbacks, and it is possible to firmly integrate the EP rubber and the adhesive material.
このような接着剤の好ましいものとしては、エチレンを
主鎖に含むエチレンビニルアセテート共重合体(Ethyle
n vinyl acetate copolymer:以下、EVAと表記する)、
メチルメタクリレート(Ethyl methacrylate:以下、EMA
と表記する)、エチレンエチルアクリレート(Ethylen
ethyl acrylate:以下、EEAと表記する)、エチレンアク
リリックアシッド(Ethylen acrylic acid:以下、EAAと
表記する)等の共重合体や有機酸グラフトEVA(以下、
酸グラフトEVAと表記する)、有機酸グラフトポリエチ
レン(以下、酸グラフトPEと表記する)、有機酸グラフ
トポリプロピレン(以下、酸グラフトPPと表記する)等
の酸グラフト共重合体を主成分とするポリオレフィン系
共重合体組成物を例示することができる。これらの主成
分を構成する共重合体は、その側鎖部分やグラフト重合
された酸部分に強い極性基を持っているので、これらの
極性基がEP系ゴムや粘着材に対して強い化学的親和性を
示し、良好な浸透性,結合性ひいては接着性を示すもの
と考えられる。A preferable example of such an adhesive is an ethylene vinyl acetate copolymer (Ethyle) containing ethylene in the main chain.
n vinyl acetate copolymer: hereafter referred to as EVA),
Methyl methacrylate (Ethyl methacrylate: Below, EMA
Notated), ethylene ethyl acrylate (Ethylen
Copolymers such as ethyl acrylate: hereinafter referred to as EEA) and ethylene acrylic acid (hereinafter referred to as EAA) and organic acid-grafted EVA (hereinafter referred to as
Polyolefins containing acid graft copolymers such as acid graft EVA), organic acid graft polyethylene (hereinafter referred to as acid graft PE), organic acid graft polypropylene (hereinafter referred to as acid graft PP), etc. Examples of the system copolymer composition include: The copolymers that make up these main components have strong polar groups in their side chains and in the acid moieties that have been graft-polymerized, so these polar groups are chemically resistant to EP rubber and adhesives. It is considered to exhibit affinity, good penetrability, bondability, and adhesiveness.
尚上記ポリオレフィン系共重合体(主成分)は、粘着材
の種類に応じて選択使用することが望ましく、例えばポ
リアクリル酸,ポリアクリル酸ブチル,ポリアクリル酸
2−エチルヘキシル等のアクリル樹脂系粘着材に対して
はEVA,EMA,EEA,EAA等の主鎖にエチレンを含む共重合体
を主成分とする接着剤組成物がより強い親和性を示し、
ポリイソプレン,SBゴム,ブチルゴム,ポリイソブチレ
ン等のゴム系粘着材に対しては、酸グラフトEVA,酸グラ
フトPE,酸グラフトPP等を主成分とする接着剤組成物が
高い親和性を示す。尚上記接着剤組成物においては、他
の配合成分としてロジン,クマロンインデン,フェノー
ル樹脂等の粘着付与剤、フタル酸エステル,リン酸エス
テル,塩化パラフィン等の可塑剤,ブチル錫系,オクチ
ル錫系等の安定剤等を添加することができる。The polyolefin-based copolymer (main component) is preferably selected and used according to the type of the adhesive material. For example, an acrylic resin-based adhesive material such as polyacrylic acid, polybutyl acrylate, poly (2-ethylhexyl acrylate), etc. In contrast, EVA, EMA, EEA, EAA, adhesive composition containing a copolymer containing ethylene in the main chain as a main component shows a stronger affinity,
For rubber-based adhesives such as polyisoprene, SB rubber, butyl rubber, and polyisobutylene, the adhesive composition containing acid-grafted EVA, acid-grafted PE, acid-grafted PP, etc. as a main component shows high affinity. In the above-mentioned adhesive composition, other compounding ingredients such as rosin, coumarone indene, tackifier such as phenol resin, phthalate ester, phosphate ester, plasticizer such as paraffin chloride, butyltin system, octyltin system, etc. It is possible to add stabilizers and the like.
又本発明における上記接着剤は熱活性型の接着剤であ
り、50℃以下では固体であって接着性を保有せず、80乃
至150℃に加熱することによって溶融し、流動し易くな
って接着性を発揮するようになるものであり、接着後、
再び50℃以下に冷却することにより、接着状態のまま固
化して元の固体状態に戻るのである。従って後述の如く
粘着剤層とEP系ゴムシートの間に介在させて、好ましく
は80乃至150℃で加熱圧締することにより接着剤として
の機能を如何なく発揮させることができる。Further, the adhesive in the present invention is a heat-activatable adhesive, which is solid at 50 ° C. or lower and does not have adhesiveness, and is melted by heating at 80 to 150 ° C. It will become effective, and after adhesion,
By cooling it to 50 ° C or lower again, it solidifies in the adhesive state and returns to the original solid state. Therefore, by interposing between the pressure-sensitive adhesive layer and the EP-based rubber sheet as described later and heating and pressing preferably at 80 to 150 ° C., the function as an adhesive can be fully exerted.
本発明に係るEP系ゴム複合体は、このような接着剤層を
介してEP系ゴム成形品と粘着材を接着してなるもので、
該EP系ゴム複合体を製造するに当たっては、例えばシー
ト状粘着材に上記接着剤を塗布あるいはフィルム状にし
て積層し、さらにその上からEP系ゴムシートを積層して
熱ロールにより加熱圧縮して一体化する方法を採用すれ
ばよいが、積層の順序は上記に限定されず、まず始めに
EP系ゴムシートに接着材層を重ね合わせ、次いで粘着材
シートを積層することも可能であり、あるいはEP系ゴム
シート,接着剤層,粘着材シートの三者を同時に積層し
て熱ロール等により一体化してもよい。The EP-based rubber composite according to the present invention is formed by adhering an EP-based rubber molded article and a pressure-sensitive adhesive through such an adhesive layer,
In producing the EP rubber composite, for example, the adhesive is applied to a sheet-like pressure-sensitive adhesive or laminated in the form of a film, and then an EP rubber sheet is laminated thereon and heated and compressed by a heat roll. The method of integration may be adopted, but the order of stacking is not limited to the above, and first,
It is also possible to stack the adhesive layer on the EP rubber sheet and then laminate the adhesive sheet, or to laminate the EP rubber sheet, adhesive layer and adhesive sheet at the same time by using a heat roll or the like. You may integrate.
尚粘着材シートには使用時まで粘着面を保護する目的で
離形紙を接着しておくことが望まれる。It is desirable that a release paper be adhered to the adhesive sheet for the purpose of protecting the adhesive surface before use.
実施例1 第1表に示す組成のゴム材料をゴム用ロールで混練して
均一に分散させ、EPゴムの未加硫ゴムを調製した。但
し、第1表中、FEFブラックはFast Extrusion Furnace
Black、SRFブラックはSemi Rein−forcing Furnace Bla
ck、MTブラックはMedium Thermal Blackの略である。ま
た、アクセルM、アクセルTMTD、アクセルPZはそれぞれ
川口化学工業(株)の商品の商品名であって、アクセル
Mは2−Mercaptobenzothiazole、アクセルTMTDはTetra
methyl Tiuram Disulfide、アクセルPZはZinc Dimethyl
Dithiocarbamateである。1.0mmのゴム板作製用金型に
未加硫ゴムを仕込み170℃に加熱した平盤熱プレスで10
分間圧締し、240×240×1.0mmのEP加硫ゴムシートを作
製した。このゴムシートの表面をトルエンを含ませたウ
エスで拭いて脱脂した。熱活性形フィルム状接着剤1
(例えばクリアタイトSA01、厚さ30μm、積水化学工業
(株)製)と、離型紙3付きアクリル樹脂系粘着材2
(例えばニット−No.500、日東電工(株)製)を第1図
のようにロール4で圧締して予備接着する。Example 1 A rubber material having the composition shown in Table 1 was kneaded with a rubber roll and uniformly dispersed to prepare an EP rubber unvulcanized rubber. However, in Table 1, FEF Black is Fast Extrusion Furnace
Black, SRF Black is Semi Rein-forcing Furnace Bla
ck and MT black are short for Medium Thermal Black. Axel M, Axel TMTD, and Axel PZ are trade names of Kawaguchi Chemical Industry Co., Ltd., where Axel M is 2-Mercaptobenzothiazole and Axel TMTD is Tetra.
methyl Tiuram Disulfide, Accel PZ is Zinc Dimethyl
Dithiocarbamate. The unvulcanized rubber was charged into a die for making a 1.0 mm rubber plate, and the flat plate heat press heated to 170 ° C
It was pressed for a minute to prepare an EP vulcanized rubber sheet of 240 × 240 × 1.0 mm. The surface of this rubber sheet was wiped with a waste cloth containing toluene for degreasing. Heat activated film adhesive 1
(For example, CLEARITE SA01, thickness 30 μm, manufactured by Sekisui Chemical Co., Ltd.) and acrylic resin adhesive 2 with release paper 3
(For example, Knit-No. 500, manufactured by Nitto Denko Co., Ltd.) is pre-bonded by pressing with a roll 4 as shown in FIG.
次いで予備接着した熱着材付き接着剤層と脱脂済みEP加
硫ゴムシート3を貼り合わせ、120℃に加熱した平盤熱
プレスで30秒間圧締して一体化した。除圧後、室温で冷
却し、切断機で例えば10mm角にカットし(第2,3図参
照)、緩衝材として使用した。従来品との接着強度の違
いを第2表に示した。Next, the pre-bonded adhesive layer with a heat-bonding material and the degreased EP vulcanized rubber sheet 3 were bonded together, and pressed by a flat plate heat press heated to 120 ° C. for 30 seconds to be integrated. After depressurization, it was cooled at room temperature, cut into a 10 mm square by a cutting machine (see FIGS. 2 and 3), and used as a cushioning material. Table 2 shows the difference in adhesive strength from the conventional product.
実施例2 長尺物の製造方法を第4図に示す。 Example 2 A method for manufacturing a long product is shown in FIG.
離形紙付き粘着材11(例えばニット−No.500、日東電工
(株)製)と熱活性形フィルム状接着剤12(例えばクリ
アタイトSB−01、厚さ100μm−積水化学工業(株)
製)をロールプレス21で圧締し、空気を除去しながら貼
合わせて仮止め状態13とし、一方カレンダーロールで成
形した長尺EP加硫ゴムシート14(例えばEPTW−160、厚
さ0.3mm、亀戸ゴム(株)製)を100℃の加熱炉22中で予
熱しつつ接着剤側と貼合わせ、120℃に加熱した加熱ロ
ールプレス23で圧締しながら30cm/分のスピードで移動
させ、離形紙付き粘着材とEP加硫ゴムシートを接合一体
化した。これを一旦ロール状に巻取った。このシートを
次工程で切断機により所定の寸法形状に離型紙の手前ま
でハーフカットし、防振材として使用した。Adhesive material 11 with release paper (for example, Knit-No.500, manufactured by Nitto Denko Corporation) and heat-activatable film adhesive 12 (for example, Cleartite SB-01, thickness 100 μm-Sekisui Chemical Co., Ltd.)
(Made) is pressed with a roll press 21 and is temporarily bonded by adhering while removing air, while a long EP vulcanized rubber sheet 14 (e.g. EPTW-160, thickness 0.3 mm) formed by a calender roll is used. Kameido Rubber Co., Ltd. is preheated in a heating furnace 22 at 100 ° C. while being bonded to the adhesive side, and is moved at a speed of 30 cm / min while being pressed with a heating roll press 23 heated to 120 ° C. An adhesive material with a pattern paper and an EP vulcanized rubber sheet are joined and integrated. This was once wound into a roll. In the next step, this sheet was half-cut to a predetermined size and shape by a cutting machine up to the front of the release paper and used as a vibration isolator.
本発明は以上のように構成されており、EP系ゴム成形品
に対し粘着材を強固に接着一体化することができるよう
になり、耐候性の優れ、しかも簡易取付けできるEP系ゴ
ム複合体(緩衝材、防振材または防音材)を提供するこ
とができた。INDUSTRIAL APPLICABILITY The present invention is configured as described above, and an adhesive material can be firmly bonded and integrated to an EP rubber molded product, which has excellent weather resistance and can be easily attached to an EP rubber composite ( Cushioning material, vibration damping material or sound insulating material).
また接着剤として熱活性形フィルム状接着剤を使用して
いるので、貼合わせ作業が非常に容易となると共に接着
強度のばらつきが少なくなり、長尺品の連続貼合わせが
可能となった。Further, since the heat-activatable film adhesive is used as the adhesive, the laminating work is very easy and the variation of the adhesive strength is reduced, and the continuous laminating of long products becomes possible.
第1図は離形紙付き粘着材と接着剤との接着状態を示す
説明図、第2,3図は緩衝材の形状を示す斜視説明図、第
4図は長尺物の製造方法を示す概略説明図である。 1……フィルム状接着剤 2,11……粘着材 3……離形紙 4,21……ロール 14……ゴムシート 22……加熱炉 23……加熱ロールプレスFIG. 1 is an explanatory view showing a bonding state of a pressure-sensitive adhesive material with release paper and an adhesive, FIGS. 2 and 3 are perspective explanatory views showing a shape of a cushioning material, and FIG. 4 shows a method for manufacturing a long product. It is a schematic explanatory drawing. 1 …… Film adhesive 2,11 …… Adhesive material 3 …… Release paper 4,21 …… Roll 14 …… Rubber sheet 22 …… Heating furnace 23 …… Heating roll press
Claims (5)
る)系ゴム成形品の少なくとも一面に熱活性形接着剤層
を介して粘着材を接着してなることを特徴とするEP系ゴ
ム複合体。1. An EP-based rubber composite comprising an ethylene / propylene (hereinafter referred to as EP) -based rubber molded article and an adhesive material bonded to at least one surface of the molded article via a heat-activatable adhesive layer. .
ビニルアセテート共重合体、エチルメタクリレート、エ
チレンエチルアクリレート、エチレンアクリリックアシ
ッド等のエチレン化合物を主成分としたポリオレフィン
系共重合体組成物である請求項(1)に記載のEP系ゴム
複合体。2. A heat-activatable adhesive is a polyolefin-based copolymer composition containing ethylene compounds such as ethylene-vinyl acetate copolymer containing ethylene, ethyl methacrylate, ethylene ethyl acrylate and ethylene acrylic acid as a main component. The EP rubber composite according to item (1).
ラフトエチレンビニルアセテート共重合体、有機酸グラ
フトポリエチレン、有機酸グラフトポリプロピレン等の
酸変成エチレン化合物を主成分としたポリオレフィン系
共重合体組成物である請求項(1)に記載のEP系ゴム複
合体。3. A polyolefin-based copolymer composition containing an acid-modified ethylene compound such as an organic acid-grafted ethylene vinyl acetate copolymer, an organic acid-grafted polyethylene, or an organic acid-grafted polypropylene as a main component, in which the heat-activatable adhesive contains ethylene. The EP rubber composite according to claim 1, which is a product.
ム系粘着材である請求項(1)乃至(3)のいずれかに
記載のEP系ゴム複合体。4. The EP rubber composite according to claim 1, wherein the adhesive is an acrylic resin adhesive or a synthetic rubber adhesive.
材の間に介装し、加熱圧締して接合一体化することを特
徴とするEP系ゴム複合体の製造方法。5. A method for producing an EP-based rubber composite, characterized in that a heat-activatable adhesive is interposed between an EP-based rubber molded article and an adhesive material, and heat-pressed to bond and integrate them.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25616489A JPH0688380B2 (en) | 1989-09-29 | 1989-09-29 | Ethylene / propylene rubber composite and method for producing the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25616489A JPH0688380B2 (en) | 1989-09-29 | 1989-09-29 | Ethylene / propylene rubber composite and method for producing the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03114828A JPH03114828A (en) | 1991-05-16 |
| JPH0688380B2 true JPH0688380B2 (en) | 1994-11-09 |
Family
ID=17288794
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP25616489A Expired - Lifetime JPH0688380B2 (en) | 1989-09-29 | 1989-09-29 | Ethylene / propylene rubber composite and method for producing the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0688380B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5411783A (en) * | 1993-03-08 | 1995-05-02 | Specialty Adhesive Film Co. | Heat activated applique with upper thermoplastic elastomer layer |
| JP3789760B2 (en) * | 2001-03-02 | 2006-06-28 | ソニーケミカル株式会社 | Hard disk drive |
| CN102286257B (en) * | 2011-06-16 | 2013-01-09 | 上海邦中高分子材料有限公司 | Special high temperature resistant adhesive resins for steel-plastic composite pipe and preparation method thereof |
-
1989
- 1989-09-29 JP JP25616489A patent/JPH0688380B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH03114828A (en) | 1991-05-16 |
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