JP2010024820A - Gasket - Google Patents

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JP2010024820A
JP2010024820A JP2009123780A JP2009123780A JP2010024820A JP 2010024820 A JP2010024820 A JP 2010024820A JP 2009123780 A JP2009123780 A JP 2009123780A JP 2009123780 A JP2009123780 A JP 2009123780A JP 2010024820 A JP2010024820 A JP 2010024820A
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layer
gasket
gasket body
base material
skin layer
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JP5610705B2 (en
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Koichi Terasaki
浩一 寺崎
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Nishikawa Rubber Co Ltd
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Nishikawa Rubber Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To prevent yellowing due to penetration of sulfur components to a surface skin layer from a gasket body, in gaskets comprising the gasket body formed of a valcanized rubber material and a resin surface skin layer formed integrally with the surface layer part of the gasket body, and being fitted into joints between outer wall panels of a building. <P>SOLUTION: In the gasket 11 comprising the gasket body 4 and the surface skin layer 5 formed in the surface layer part 3 of the gasket body 4 through an adhesive layer 12, the adhesive layer 12 includes an intermediate base material layer formed of a metal foil for blocking the penetration of sulfur components from the gasket body 4 to the surface skin layer 5 and an outer layer comprising polyethylene to be applied to both sides of the intermediate base material layer, and at the same time as when it is valcanized by heating after extrusion molding, the polyethylene melts and adheres the intermediate base material layer, the gasket body 4 and the outer layer. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

本発明は、建物の外壁パネル間の目地に装着されるガスケットに関する。   The present invention relates to a gasket attached to a joint between outer wall panels of a building.

図1は、従来のガスケットの一例を示すもので、柱部1と、該柱部1の両側より斜め上向きに突出形成されるリップ2と、柱部1の上端から両側方に突出形成され、目地装着時に目地の屋外側を向く表層部3からなり、シール(防水)を目的としたガスケット本体4と、表層部3の表面に一体形成され、耐候性及び意匠性を備えた表皮層5からなり、ガスケット本体4は多くがEPM、EPDM等の加硫ゴム材料から、表皮層5はオレフィン系又はスチレン系熱可塑性樹脂(TPE)、塩素系ポリエチレン(CPE)、EPDM等のゴム材料からなっている。またアクリル樹脂、ABS樹脂、AES樹脂等よりなる表皮材と、EPDMよりなるガスケット本体との接着性を向上させるために両者間にポリエチレン層を介在させたものも知られる(特許文献1)。   FIG. 1 shows an example of a conventional gasket, which is formed with a column 1, a lip 2 that is formed to project obliquely upward from both sides of the column 1, and a projection that protrudes on both sides from the upper end of the column 1. It consists of a surface layer 3 that faces the outside of the joint when the joint is mounted, a gasket body 4 for sealing (waterproofing), and a skin layer 5 that is integrally formed on the surface of the surface layer 3 and has weather resistance and design. The gasket body 4 is mostly made of a vulcanized rubber material such as EPM and EPDM, and the skin layer 5 is made of a rubber material such as olefin-based or styrene-based thermoplastic resin (TPE), chlorinated polyethylene (CPE), EPDM, etc. Yes. Moreover, in order to improve the adhesiveness of the skin material which consists of acrylic resin, ABS resin, AES resin, etc., and the gasket main body which consists of EPDM, what interposed the polyethylene layer between both is also known (patent document 1).

特開2005−90178号JP-A-2005-90178

図1に示す従来のガスケットは、ガスケット本体と表皮層とによりシール性と共に耐候性及び意匠性に優れるが、経年により加硫ゴム材料からなるガスケット本体から表皮層に硫黄分等が浸透し、表皮層を黄変させる懸念がある。この対策として架橋剤に硫黄や硫黄化合物に代えて有機過酸化物を用いることも行われているが、この場合、臭気が発生したり、加熱による架橋時において、介在する酸素により架橋阻害を来たして表面がネチャネチャとした状態の表面タックを来たすようになり、表面タックを回避するには架橋時に酸素を除去することができる専用の架橋炉が必要となる。   The conventional gasket shown in FIG. 1 has excellent sealing properties as well as weather resistance and design properties due to the gasket main body and the skin layer, but the sulfur content penetrates into the skin layer from the gasket main body made of vulcanized rubber material over time, and the skin There is a concern of yellowing the layer. As countermeasures, it is also possible to use organic peroxides instead of sulfur or sulfur compounds as cross-linking agents. In this case, odor is generated, or cross-linking is inhibited by intervening oxygen during cross-linking by heating. As a result, a surface tack with the surface becoming sticky is brought about, and in order to avoid the surface tack, a dedicated crosslinking furnace capable of removing oxygen at the time of crosslinking is required.

ガスケット本体を硫黄を含まない熱可塑性樹脂材料で形成したものもあり、この場合、上述するような硫黄分による黄変の問題は生じないが、樹脂材料に含まれる可塑材(オイル)が表皮層に浸透し、外観劣化の懸念がある。   Some gasket bodies are made of a thermoplastic resin material that does not contain sulfur. In this case, the problem of yellowing due to sulfur as described above does not occur, but the plastic material (oil) contained in the resin material is the skin layer. There is concern about deterioration of appearance.

本発明の目的は、ガスケット本体と、該本体の表層部に一体形成される表皮層からなるガスケットにおいて、ガスケット本体から表皮層へ架橋剤、架橋促進剤又は可塑材等の汚染懸念物質が浸透することによる外観品質の低下を防止しようとするものである。   An object of the present invention is a gasket comprising a gasket main body and a skin layer integrally formed on the surface layer portion of the main body, and a contamination concern substance such as a crosslinking agent, a crosslinking accelerator or a plastic material penetrates from the gasket main body to the skin layer. It is intended to prevent the deterioration of the appearance quality due to the above.

請求項1に係る発明は、架橋した熱硬化性材料からなるか、或いは熱可塑性樹脂材料からなり、目地装着時に目地の屋外側を向く表層部を備えたガスケット本体と、該ガスケット本体の表層部に接着材層を介して形成される表皮層からなるガスケットにおいて、前記接着材層がガスケット本体から表皮層への架橋剤、架橋促進剤又は可塑材等の汚染懸念物質の浸透を阻害する中間基材層と、その両側に被覆され、ガスケット本体及び表皮層との接着性を有する外層よりなることを特徴とする。
ここで熱硬化性材料とは、熱により硬化反応が促進される材料であり、熱可塑性樹脂とは、熱により可塑化される材料をいう。
The invention according to claim 1 is a gasket body made of a cross-linked thermosetting material or a thermoplastic resin material, and having a surface layer portion facing the outdoor side of the joint when the joint is mounted, and a surface layer portion of the gasket body In the gasket comprising the skin layer formed through the adhesive layer, the adhesive layer inhibits the penetration of the contaminants such as the crosslinking agent, crosslinking accelerator or plasticizer from the gasket body to the skin layer. It is characterized by comprising a material layer and an outer layer coated on both sides thereof and having adhesion to the gasket body and the skin layer.
Here, the thermosetting material is a material whose curing reaction is accelerated by heat, and the thermoplastic resin is a material that is plasticized by heat.

請求項2に係る発明は、請求項1に係る発明のガスケット本体が硫黄により架橋した熱硬化性材料からなることを特徴とし、
請求項3に係わる発明は、請求項1又は2に係わる発明の中間基材層13は酸素透過度が120cc/m2・24hr・atm以下の材質であることを特徴とする。
請求項4に係る発明は、請求項1ないし3に係る発明の接着材層の外層がポリエチレンであることを特徴とする。
The invention according to claim 2 is characterized in that the gasket body of the invention according to claim 1 is made of a thermosetting material crosslinked with sulfur,
The invention according to claim 3 is characterized in that the intermediate base material layer 13 of the invention according to claim 1 or 2 is made of a material having an oxygen permeability of 120 cc / m 2 · 24 hr · atm or less.
The invention according to claim 4 is characterized in that the outer layer of the adhesive layer of the invention according to claims 1 to 3 is polyethylene.

請求項1に係る発明のガスケットによると、シール性と共に耐候性及び意匠性を持たせることができること、ガスケット本体から表皮層への汚染懸念物質、例えば硫黄分や可塑材の浸透が中間基材層により阻害され、表皮層の黄変や変色等を防止できることなどの効果を有する。また中間基材層がアルミ等の金属箔よりなる場合、表皮層への汚染懸念物質の浸透を阻害する効果が大である反面、単層ではガスケット本体や表皮層との接着が困難であるが、接着性を有する外層で被覆することによりガスケット本体や表皮層との接着が容易となる。   According to the gasket of the first aspect of the present invention, the intermediate base material layer can be provided with weatherability and designability as well as sealing properties, and contamination of the gasket body from the gasket body to the skin layer, such as sulfur and plastic material. And has the effect of preventing yellowing or discoloration of the skin layer. In addition, when the intermediate base layer is made of a metal foil such as aluminum, the effect of inhibiting the penetration of substances of concern to the skin layer is great, but with a single layer, it is difficult to adhere to the gasket body or the skin layer. By coating with an outer layer having adhesiveness, adhesion to the gasket body or the skin layer is facilitated.

請求項2に係る発明のガスケットによると、押出成形後、加熱することにより加硫される。
請求項3に係わる発明のガスケットのように、中間基材層に120cc/m2・24hr・atm以下のフィルムを用いると、汚染懸念物質の浸透による色素の変化(移行汚染)を少なくすることができる。ここでcc/m2・24hr・atmとは、大気圧で24時間経過したときの1平方メートル当たりの浸透量(cc)を示す。
According to the gasket of the invention according to claim 2, it is vulcanized by heating after extrusion.
If a film of 120 cc / m 2 · 24 hr · atm or less is used for the intermediate base material layer as in the gasket of the invention according to claim 3, the change of dye (migration contamination) due to the penetration of the contaminants of concern can be reduced. it can. Here, cc / m 2 · 24 hr · atm indicates the permeation amount (cc) per square meter when 24 hours have passed at atmospheric pressure.

請求項4に係る発明のガスケットによると、加熱することによりポリエチレンが熱融解して中間基材層とガスケット本体及び表皮層との接着が行われる。   According to the gasket of the invention of claim 4, when heated, the polyethylene is thermally melted, and the intermediate base material layer, the gasket main body and the skin layer are bonded.

従来のガスケットの断面図。Sectional drawing of the conventional gasket. 本発明に係るガスケットの断面図。Sectional drawing of the gasket which concerns on this invention. 図2に示すガスケットの中間基材層の断面図。Sectional drawing of the intermediate | middle base material layer of the gasket shown in FIG. 試験片の断面図。Sectional drawing of a test piece. フィルムの断面図。Sectional drawing of a film.

以下、本発明の実施形態のガスケットについて図面により説明する。図中、図1に示すガスケットと同一構造部分には同一符号を付してその説明を省略する。   Hereinafter, a gasket according to an embodiment of the present invention will be described with reference to the drawings. In the figure, the same structural parts as those of the gasket shown in FIG.

図2に示すガスケット11は、図1に示すガスケットにおいて、ガスケット本体4と表層部3との間に接着材層12を介在させたもので、ガスケット本体4は、例えば硫黄、硫黄化合物、有機過酸化物等を架橋剤として架橋したEPDM,EPM,ウレタンゴム、シリコーンゴム、天然ゴム等の熱硬化性材料により形成され、表皮層5は、例えばオレフィン系、スチレン系、ウレタン系、エステル系等の熱可塑性樹脂材料により形成される。また接着材層12は図3に示すように、汚染懸念物質である硫黄分や可塑材等の浸透を阻害する中間基材層13と、その両側に被覆され、中間基材層13とガスケット本体4及び表皮層5との接着性を有する外層14よりなり、中間基材層13は例えばアルミ箔等の金属箔、ナイロン、エチレンビニルアルコール共重合体(EVOH)、ポリエチレンテレフタレート(PET)等により形成され、外層14は例えば直鎖状低密度ポリエチレン(LLDPE)により形成される。中間基材層13は、上述する材料に限定されるものではなく、硫黄分や可塑材の浸透を阻害するものであれば、どのような材料を用いてもよい。また外層14もガスケット本体、表層部、中間基材層を形成する材料と接着性を有すれば、直鎖状低密度ポリエチレン(LLPDE)に限定されることなく、どのような材料を用いてもよい。例えば中間基材層に塗布されるプライマー及び接着剤を用いることもできる。   A gasket 11 shown in FIG. 2 is obtained by interposing an adhesive layer 12 between the gasket body 4 and the surface layer portion 3 in the gasket shown in FIG. The outer skin layer 5 is formed of a thermosetting material such as EPDM, EPM, urethane rubber, silicone rubber, natural rubber or the like crosslinked with an oxide or the like as a crosslinking agent. The skin layer 5 is made of, for example, olefin, styrene, urethane, ester, or the like. It is formed of a thermoplastic resin material. Further, as shown in FIG. 3, the adhesive layer 12 is coated on both sides of the intermediate base material layer 13 that inhibits the penetration of sulfur and plastic materials, which are contaminants, and the intermediate base material layer 13 and the gasket body. 4 and an outer layer 14 having adhesiveness with the skin layer 5, and the intermediate base layer 13 is formed of, for example, metal foil such as aluminum foil, nylon, ethylene vinyl alcohol copolymer (EVOH), polyethylene terephthalate (PET), or the like. The outer layer 14 is made of, for example, linear low density polyethylene (LLDPE). The intermediate base material layer 13 is not limited to the materials described above, and any material may be used as long as it inhibits the sulfur content and the penetration of the plastic material. The outer layer 14 is not limited to linear low-density polyethylene (LLPDE) as long as it has adhesiveness with the material forming the gasket body, surface layer portion, and intermediate base material layer, and any material can be used. Good. For example, a primer and an adhesive applied to the intermediate base material layer can also be used.

実験例1
図4に示すように、JIS A硬度70の硫黄を加硫剤として用いたEPDMよりなる厚さ2mmの下地材16上にフィルム層17を介してオレフィン系熱可塑性エラストマー(TPO)よりなる厚さ1mmのカラー材18を重ね、プレス機で圧着して幅20mm、長さ50mmの試験片19を作成した。フィルム層17は厚み40μmのナイロンの両面にLLPDEを積層してなるものである。
Experimental example 1
As shown in FIG. 4, a thickness made of olefin-based thermoplastic elastomer (TPO) through a film layer 17 on a base material 16 made of EPDM using JIS A hardness 70 sulfur as a vulcanizing agent. A test piece 19 having a width of 20 mm and a length of 50 mm was prepared by stacking 1 mm of color material 18 and pressing with a press. The film layer 17 is formed by laminating LLPDE on both sides of nylon having a thickness of 40 μm.

次に上記試験片19に対し、ダイプラウインテス社製の耐候促進試験機(メタルウェザーKU−R5CI−A)を用いて耐候試験を行った。
試験は試験片19に対し、下記表1に示す条件にて(1)紫外線の照射、(2)紫外線の照射を停止した暗闇の暗黒状態、(3)結露を各4時間ずつ(1)、(2)、(3)の順に繰返し計100〜500hr行った。
Next, the test piece 19 was subjected to a weather resistance test using a weather resistance accelerated tester (Metal Weather KU-R5CI-A) manufactured by Daipla Intes.
The test was performed on the test piece 19 under the conditions shown in Table 1 below: (1) UV irradiation, (2) darkness in the dark when UV irradiation was stopped, (3) condensation for 4 hours each (1), A total of 100 to 500 hours was repeated in the order of (2) and (3).


なお、上記(1)と(3)の処理では処理開始前の10秒間、ph6〜8、10Ω・cm以上の脱イオン水を散水した。

In the treatments (1) and (3), deionized water of ph 6-8, 10 5 Ω · cm or more was sprinkled for 10 seconds before the treatment was started.

上述の耐候試験後の試験片19について、カラーコンピュータを用いてJIS Z8729に規定されるL*、a*、b*を測定し、試験前と試験後の差ΔL* 、Δ*a 、Δ*bを求めて下記数1式により試験前と試験後の色差ΔE*abを求めた。その結果を以下の表2に示す。表中、100hrは上述の試験(1)、(2)、(3)を繰返し行った合計時間を示す。200〜500hrについても同様の合計時間を示す。   About the test piece 19 after the above-mentioned weather resistance test, L *, a *, b * defined in JIS Z8729 are measured using a color computer, and the difference ΔL *, Δ * a, Δ * before and after the test is measured. b was determined, and the color difference ΔE * ab before and after the test was determined by the following equation (1). The results are shown in Table 2 below. In the table, 100 hr indicates the total time in which the above tests (1), (2), and (3) were repeated. The same total time is shown for 200 to 500 hours.

実験例2
実験例1の試験片19において、フィルム層17を構成するナイロンを厚さ50μmのエチレンビニルアルコール共重合体EVOHとした以外は、実験例1と同じ材質の試験片を作成し、実験例1と同じく表1に示す条件にて耐候試験を行った。次に実験例1と同様の方法により100〜500hrでの色差ΔE*abを求めた。結果を以下の表2に示す。
Experimental example 2
In the test piece 19 of Experimental Example 1, a test piece made of the same material as that of Experimental Example 1 was prepared except that the nylon constituting the film layer 17 was an ethylene vinyl alcohol copolymer EVOH having a thickness of 50 μm. Similarly, a weather resistance test was performed under the conditions shown in Table 1. Next, the color difference ΔE * ab at 100 to 500 hr was determined by the same method as in Experimental Example 1. The results are shown in Table 2 below.

実験例3
実験例1の試験片19において、フィルム層17を図5に示すように、ポリエチレンテレフタレートフィルム(PET)22の表面にアルミ23を蒸着(PETとの合計厚み12μm)して、その両面にLLDPEを積層したフィルム21層とした以外は、実験例1の試験片と同様の試験片を作成し、実験例1と同じく表1に示す条件にて耐候試験を行った。次に実験例1と同様の方法により100〜200hrでの色差ΔE*abを求めた。結果を以下の表2に示す。
Experimental example 3
In the test piece 19 of Experimental Example 1, the film layer 17 was vapor-deposited on the surface of a polyethylene terephthalate film (PET) 22 (total thickness of 12 μm with PET) as shown in FIG. Except for the laminated film 21 layer, a test piece similar to the test piece of Experimental Example 1 was prepared, and the weather resistance test was performed under the conditions shown in Table 1 as in Experimental Example 1. Next, the color difference ΔE * ab at 100 to 200 hours was determined by the same method as in Experimental Example 1. The results are shown in Table 2 below.

比較例1
実験例1の試験片19において、フィルム層17を除いた試験片、すなわち下地材16上にカラー材18を積層した試験片を作成し、実験例1と同じく表1に示す条件にて耐候試験を行った。次に実験例1と同様の方法により100〜500hrでの色差ΔE*abを求めた。結果を以下の表2に示す。
Comparative Example 1
In the test piece 19 of Experimental Example 1, a test piece excluding the film layer 17, that is, a test piece in which the color material 18 is laminated on the base material 16, was prepared, and the weather resistance test was performed under the conditions shown in Table 1 as in Experimental Example 1. Went. Next, the color difference ΔE * ab at 100 to 500 hr was determined by the same method as in Experimental Example 1. The results are shown in Table 2 below.

比較例2
実験例1の試験片19において、フィルム層17を厚さ30μmのポリエチレン(PE)フィルムの単層とした以外は実験例1と同じ材質の試験片を用い、実験例1と同じく表1に示す条件にて耐候試験を行った。次に実験例1と同様の方法により100〜200hrでの色差ΔE*abを求めた。結果を以下の表2に示す。
Comparative Example 2
In the test piece 19 of Experimental Example 1, a test piece made of the same material as that of Experimental Example 1 is used except that the film layer 17 is a single layer of a polyethylene (PE) film having a thickness of 30 μm. A weather resistance test was performed under the conditions. Next, the color difference ΔE * ab at 100 to 200 hours was determined by the same method as in Experimental Example 1. The results are shown in Table 2 below.

参考例
実験例1の試験片19のカラー材単体(全体をオレフィン系熱可塑性エラストマー(TPO)で形成した試験片)に対し、実験例1と同じく表1に示す条件にて耐候試験を行った。次に実験例1と同様の方法により100〜500hrでの色差ΔE*abを求めた。結果を以下の表2に示す。
Reference Example A weather resistance test was performed on the color material alone of the test piece 19 of Test Example 1 (a test piece formed entirely of an olefin-based thermoplastic elastomer (TPO)) under the conditions shown in Table 1 as in Test Example 1. . Next, the color difference ΔE * ab at 100 to 500 hr was determined by the same method as in Experimental Example 1. The results are shown in Table 2 below.

表2に示されるように、TPOのみで作成される参考例の試験片は表面の変色が小であるのに対し、比較例1の試験片は耐候試験の結果、EPDMの硫黄分による汚染がTPOに浸透し、表面に析出して黄変する変色が大であった。また比較例1に示されるように下地材16とカラー材18との間にポリエチレンフィルムを介在させても汚染物質の移行防止効果はなく、表面の黄変が大となった。これに対し、実験例1〜3は、比較例1及び2に比べ、下地材16からカラー材18への汚染物質の移行防止効果が良好で、カラー材表面の変色が大幅に減少した。なお、実験例3はフィルムをアルミ蒸着PETとし、アルミ層とPET層の2層構造とするものであるが、アルミ単体又はPET単体でも充分な効果を達成することができる。   As shown in Table 2, the test piece of the reference example made only with TPO has a small surface discoloration, whereas the test piece of Comparative Example 1 shows the contamination by the sulfur content of EPDM as a result of the weather resistance test. The discoloration that penetrated TPO, deposited on the surface and yellowed was large. Further, as shown in Comparative Example 1, even if a polyethylene film was interposed between the base material 16 and the color material 18, there was no effect of preventing the migration of contaminants, and the surface yellowed greatly. On the other hand, Experimental Examples 1 to 3 were more effective in preventing the migration of contaminants from the base material 16 to the color material 18 than in Comparative Examples 1 and 2, and the discoloration of the color material surface was greatly reduced. In Experimental Example 3, the film is made of aluminum vapor-deposited PET and has a two-layer structure of an aluminum layer and a PET layer. However, sufficient effects can be achieved with aluminum alone or PET alone.

表3は、株式会社日報により1999年4月1日に発行された「新・食品包装用フィルム」187頁・表8−1に記載され、JIS K 7126に基づいて求められた「各種プラスチックフィルムの酸素・水蒸気透過度」より抜粋された各種プラスチックフィルムの酸素透過度を示すものである。   Table 3 is described in “New Food Packaging Film” on page 187 and Table 8-1 issued by Nikkan Co., Ltd. on April 1, 1999, and “various plastic films” obtained based on JIS K 7126. The oxygen permeability of various plastic films extracted from “Oxygen / Water Vapor Permeability”.

中間基材層にナイロン、エチレンビニルアルコール共重合体EVOH、アルミ蒸着ポリエチレンテレフタレートPETを用いた場合、表2に示すように色差ΔE*abが小さくなるが、これらのフィルムは表3に示されるように、エチレン・酢酸ビニル共重合体、低密度ポリエチレンに比べ、酸素透過度が大幅に低下しており、このことより酸素透過度の小さいフィルムは色差ΔE*abも小さくなる傾向となることが分かる。とくに酸素透過度が120cc/m2・24hr・atm以下の材質である、表中のポリエチレンテレフタレート、延伸ナイロン、エチレンビニルアルコール共重合体、アルミ箔積層フィルムは、他のエチレン酢酸ビニル共重合体・低密度ポリエチレンに比べ酸素透過度が際立って小さく、色差も格段に小さくなっている。 When nylon, ethylene vinyl alcohol copolymer EVOH, and aluminum-deposited polyethylene terephthalate PET are used for the intermediate base material layer, the color difference ΔE * ab is small as shown in Table 2, but these films are shown in Table 3. In addition, compared with ethylene / vinyl acetate copolymer and low-density polyethylene, the oxygen permeability is greatly reduced. From this, it is understood that a film having a low oxygen permeability tends to have a small color difference ΔE * ab. . In particular, polyethylene terephthalate, stretched nylon, ethylene vinyl alcohol copolymer, aluminum foil laminated film in the table, whose oxygen permeability is 120cc / m 2 · 24hr · atm or less, are other ethylene vinyl acetate copolymers, Compared to low-density polyethylene, the oxygen permeability is remarkably small, and the color difference is remarkably small.

なお、各種フィルムの酸素透過度は厚みによって多少変化する可能性はあるが、変化するにしても、エチレン酢酸ビニル共重合体やポリエチレンほど飛躍的に上がることはない、と考えられる。   In addition, although the oxygen permeability of various films may change a little with thickness, even if it changes, it is thought that it does not rise as much as ethylene vinyl acetate copolymer and polyethylene.

1・・柱部
2・・リップ
3・・表層部
4・・ガスケット本体
5・・表皮層
11・・ガスケット
12・・接着材層
13・・中間基材層
14・・外層
16・・下地材
17、21・・フィルム層
18・・カラー材
19・・試験片
22・・PET
23・・アルミ
24・・LLDPE
1 .. Column part 2 .. Lip 3 .. Surface layer part 4 .. Gasket body 5 .. Skin layer 11 .. Gasket 12 .. Adhesive layer 13 .. Intermediate base material layer 14 .. Outer layer 16. 17, 21 ... Film layer 18 Color material 19 Test piece 22 PET
23 .. Aluminum 24 .. LLDPE

Claims (4)

架橋した熱硬化性材料からなるか、或いは熱可塑性樹脂材料からなり、目地装着時に目地の屋外側を向く表層部3を備えたガスケット本体4と、該ガスケット本体4の表層部に接着材層12を介して形成される表皮層5からなるガスケット11において、前記接着材層12がガスケット本体4から表皮層5への架橋剤、架橋促進剤又は可塑材等の汚染懸念物質の浸透を阻害する中間基材層13と、その両側に被覆され、ガスケット本体4及び表皮層5との接着性を有する外層14よりなることを特徴とするガスケット。   A gasket body 4 made of a cross-linked thermosetting material or a thermoplastic resin material and having a surface layer portion 3 facing the outdoor side of the joint when the joint is mounted, and an adhesive layer 12 on the surface layer portion of the gasket body 4 In the gasket 11 composed of the skin layer 5 formed through the intermediate layer, the adhesive layer 12 inhibits the penetration of the contaminants such as a crosslinking agent, a crosslinking accelerator or a plastic material from the gasket body 4 to the skin layer 5. A gasket comprising a base material layer 13 and an outer layer 14 which is coated on both sides thereof and has adhesiveness to the gasket body 4 and the skin layer 5. 前記ガスケット本体4が硫黄により架橋した熱硬化性材料からなることを特徴とする請求項1記載のガスケット。   The gasket according to claim 1, wherein the gasket body (4) is made of a thermosetting material crosslinked with sulfur. 前記中間基材層13は、酸素透過度が120cc/m2・24hr・atm以下の材質であることを特徴とする請求項1又は2記載のガスケット。 The gasket according to claim 1, wherein the intermediate base material layer 13 is made of a material having an oxygen permeability of 120 cc / m 2 · 24 hr · atm or less. 接着材層12の外層14がポリエチレンであることを特徴とする請求項1ないし3記載のガスケット。   4. The gasket according to claim 1, wherein the outer layer 14 of the adhesive layer 12 is polyethylene.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013001696A1 (en) * 2011-06-30 2013-01-03 三洋電機株式会社 Solar cell module
JP2015212509A (en) * 2014-04-17 2015-11-26 東海興業株式会社 Molding
JP2016014119A (en) * 2014-07-03 2016-01-28 住友ゴム工業株式会社 Paramagnetic radical-doped polymer material storage method

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03240530A (en) * 1990-02-19 1991-10-25 Toyoda Gosei Co Ltd Rubber laminate with finished film layer
JPH08135034A (en) * 1994-11-05 1996-05-28 Inoac Corp Dwelling house gasket
JPH10266369A (en) * 1997-03-21 1998-10-06 Shin Etsu Polymer Co Ltd Silicone joint member with metal foil and silicone joint structure employing this
JP2005090178A (en) * 2003-09-19 2005-04-07 Nishikawa Rubber Co Ltd Gasket for joint

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03240530A (en) * 1990-02-19 1991-10-25 Toyoda Gosei Co Ltd Rubber laminate with finished film layer
JPH08135034A (en) * 1994-11-05 1996-05-28 Inoac Corp Dwelling house gasket
JPH10266369A (en) * 1997-03-21 1998-10-06 Shin Etsu Polymer Co Ltd Silicone joint member with metal foil and silicone joint structure employing this
JP2005090178A (en) * 2003-09-19 2005-04-07 Nishikawa Rubber Co Ltd Gasket for joint

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013001696A1 (en) * 2011-06-30 2013-01-03 三洋電機株式会社 Solar cell module
JP2015212509A (en) * 2014-04-17 2015-11-26 東海興業株式会社 Molding
JP2016014119A (en) * 2014-07-03 2016-01-28 住友ゴム工業株式会社 Paramagnetic radical-doped polymer material storage method

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