JPS6076561A - Resin composition - Google Patents

Resin composition

Info

Publication number
JPS6076561A
JPS6076561A JP58184089A JP18408983A JPS6076561A JP S6076561 A JPS6076561 A JP S6076561A JP 58184089 A JP58184089 A JP 58184089A JP 18408983 A JP18408983 A JP 18408983A JP S6076561 A JPS6076561 A JP S6076561A
Authority
JP
Japan
Prior art keywords
resin composition
examples
weight
glass
silicone oil
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.)
Granted
Application number
JP58184089A
Other languages
Japanese (ja)
Other versions
JPS6126948B2 (en
Inventor
Yukio Kawakita
川北 幸男
Masayuki Goto
正行 後藤
Hitoshi Hasegawa
均 長谷川
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toyoda Gosei Co Ltd
Original Assignee
Toyoda Gosei Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Toyoda Gosei Co Ltd filed Critical Toyoda Gosei Co Ltd
Priority to JP58184089A priority Critical patent/JPS6076561A/en
Publication of JPS6076561A publication Critical patent/JPS6076561A/en
Publication of JPS6126948B2 publication Critical patent/JPS6126948B2/ja
Granted legal-status Critical Current

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  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:A resin composition, obtained by incorporating a thermoplastic elastomer with a silicone oil and ''Teflon'' powder inspecific amounts, having flexibility, low frictional resistance and improved abrasion resistance. CONSTITUTION:A resin composition obtained by incorporating (A) 100pts.wt. thermoplastic elastomer, e.g. styrene, urethane or copolyester, with (B) 1-50pts. wt., preferably 5-20pts.wt. silicone oil and (C) 5-200pts.wt., preferably 10- 30pts.wt. ''Teflon'' powder. The incorporation of the components (B) and (C) enhances the lubricity and reduces the coefficient of friction. USE:Automotive weather strips such as glass runs, glass outers, etc.

Description

【発明の詳細な説明】 技術分野 本発明は柔軟性を有し摩擦抵抗が小さく、耐摩耗性に優
れ、ガラスや塗装板金等の他部材と固着しにくい樹脂組
成物に関するものである、従来技術 一般に、グラスランあるいはグラスアウター等の自動車
用ウェザ−ストリップは、ゴムや軟質PVC等を素材と
している。この場合他部材とのシール性を損わず、摺動
抵抗(摩擦係数)の低下、耐摩耗性の向上及び固着防止
の目的として、ナイロン短繊維の植毛、ウレタン系塗r
1やシリコーン系塗料等の塗装などの表面処理が行われ
る。しかしこれらは処理工程が複雑で設備費が高く、従
って製造コストが高くなるうえ、必ずしも充分な製品性
能は得られ<Zかった。そこで、植毛や塗装のかわりに
、ポリエチレン、熱可塑性ウレタン等の樹脂組成物をコ
ーディングすることによって、処理工程が簡略化された
が、いずれの場合にも前)ホした摩擦係数、耐摩耗性及
び固着力の全てを満足するに至らなかった。
Detailed Description of the Invention Technical Field The present invention relates to a resin composition that is flexible, has low frictional resistance, has excellent abrasion resistance, and is difficult to adhere to other members such as glass or painted sheet metal. Generally, automotive weather strips such as glass runs or glass outerwear are made of rubber, soft PVC, or the like. In this case, for the purpose of reducing sliding resistance (friction coefficient), improving wear resistance, and preventing sticking without impairing sealing performance with other parts, nylon short fiber flocking, urethane coating, etc.
Surface treatment such as coating with 1 or silicone paint is performed. However, these methods have complicated processing steps and high equipment costs, resulting in high manufacturing costs, and they do not always provide sufficient product performance. Therefore, instead of flocking or painting, the treatment process was simplified by coating with a resin composition such as polyethylene or thermoplastic urethane, but in either case, the friction coefficient, wear resistance, etc. The adhesion force was not completely satisfied.

発明の目的 本発明は上記欠陥を解消するために成されたものであっ
て、その目的は摩擦係数が小さく、耐摩耗性に優れ、し
かも他部材に対する固着力が小さい樹脂組成物を提供す
ることにある。
Purpose of the Invention The present invention was accomplished in order to eliminate the above-mentioned defects, and its purpose is to provide a resin composition that has a low coefficient of friction, excellent wear resistance, and has low adhesion to other members. It is in.

発明の構成 本発明は」:開目的を達成するため、100重吊部の熱
可塑性エラグ]へマーと、1〜50重量部のシリコーン
オイルと、5〜200重量部のテフロンパウダーとによ
り樹脂組成物を構成している。
Structure of the Invention The present invention has been developed by: In order to achieve the object, a resin composition is made of a thermoplastic elastomer with a 100-layer suspension, a hemmer, 1 to 50 parts by weight of silicone oil, and 5 to 200 parts by weight of Teflon powder. constitutes things.

ぞこで、前述した各成分の特性あるいは配合量等につい
て説明する。
Now, the characteristics, blending amount, etc. of each of the above-mentioned components will be explained.

本発明の樹脂組成物の主成分である熱可塑性ニラストン
−には、スヂレン系、ウレタン系、コポリエステル系あ
るいはナイロン系等があり、特に種類は限定されない。
The thermoplastic Nilastone which is the main component of the resin composition of the present invention includes styrene type, urethane type, copolyester type, nylon type, etc., and the type thereof is not particularly limited.

該エラストマーは適度な柔軟性により相手部材とのシー
ル性を良好にし、各成分のバインダーとしての効果が大
ぎく耐摩耗性の低下を防ぐ。
The elastomer provides good sealing properties with the mating member due to its appropriate flexibility, and the effectiveness of each component as a binder prevents a decrease in wear resistance.

又、シリコーンオイルは樹脂組成物の潤滑性を高め摩擦
係数を低下させる作用がある。このシリコーンオイルは
1重量部以下では潤滑性か悪く、50ffili部以上
では加工性が低下するので、5〜20重量部が望ましい
Furthermore, silicone oil has the effect of increasing the lubricity of the resin composition and lowering the coefficient of friction. If the silicone oil is less than 1 part by weight, the lubricity will be poor, and if it is more than 50 parts by weight, the processability will deteriorate, so it is preferably from 5 to 20 parts by weight.

同様に、テフロンパウダーも潤滑性を高め、摩擦係数を
低下させる。これは5重量部以下では効果が小さく、1
00重量部以上では機械的強度が著しく低下するので問
題があり、10〜50重量部が望ましい。さらに、この
テフロンパウダーはゴム、樹脂あるいは金属等の5”4
種物質にコーティング又はインリート成ハリする際、溶
融された状態で樹脂組成物の表面自由エネルギーを減少
しく表面張力の低下)相手側物質の表面への喰い込みを
良くし密着力(接着性)を向」−する作用がある。
Similarly, Teflon powder also increases lubricity and reduces the coefficient of friction. This effect is small below 5 parts by weight;
If the amount exceeds 0.00 parts by weight, the mechanical strength will be significantly lowered, causing a problem, and 10 to 50 parts by weight is desirable. In addition, this Teflon powder can be used on rubber, resin, metal, etc.
When forming a coating or infiltration on a seed material, it reduces the surface free energy of the resin composition in the molten state (reduces surface tension), improves the biting into the surface of the other material, and improves adhesion (adhesion). It has the effect of "directing".

発明の効果 − 以上3つの成分から構成された本発明の樹脂組成物は、
後述する実施例の評価結果から明らかなように、従来(
比較例1〜3)と対比して摩擦係数が低く耐摩耗性に優
れかつガラス等の他部材に対する固着力を低下させるこ
とができ、さらにゴム等に対する密着力を向上すること
ができる効果を奏する。従って、例えばクラスラン、グ
ラスアウター等の自動車用ウェザ−ストリップに好適で
ある。
Effect of the invention - The resin composition of the present invention composed of the above three components,
As is clear from the evaluation results of the examples described later, conventional (
Compared to Comparative Examples 1 to 3), it has a low coefficient of friction, excellent wear resistance, can reduce the adhesion force to other members such as glass, and has the effect of improving the adhesion force to rubber etc. . Therefore, it is suitable for automobile weather strips such as classlan and glass outerwear.

実施例 次に、本発明の詳細な説明するが、その前に摩擦係数、
耐摩耗性、固着力及びゴムに塗布した場合の剥H1力(
密着力)の測定方法について説明する。
EXAMPLE Next, the present invention will be explained in detail, but before that, the friction coefficient,
Abrasion resistance, adhesion strength, and peeling force when applied to rubber (
The method for measuring adhesion strength will be explained below.

j、ず、摩擦係数の測定は、厚さ21+10のEPDM
ゴム基々イ2aの表面に対し樹脂組成物をコーティング
して厚さ0.3IIIIlの塗膜2bを形成したシー1
−から−辺が50a+mの正方形をなす試験片2を用意
でる。そして、第1図に示すように鉄板1の下面に対し
両面テープにより試験片2のゴム基材2a側を接着し、
試験片2の塗膜2b側をガラス板3の上面に載置して重
り4によって鉄板1上に荷重を加える。そして、鉄板1
に止着したワイヤー5を図示しないテンシロン型引張試
験機により毎分1001IIIIlの速度で引張って測
定される。このどき、小り4の重量W1と鉄板1の重量
W2と両面テープの重量W3とを加算したものが1kg
になるように設定される。なお、ガラス板3の上面は測
定の都度トリクロールエチレンを用いて脱脂洗浄される
j, zu, The friction coefficient was measured using EPDM with a thickness of 21+10.
Seat 1 in which a coating film 2b having a thickness of 0.3IIIl was formed by coating the surface of the rubber base 2a with a resin composition.
A test piece 2 having a square shape with sides 50a+m from - to - is prepared. Then, as shown in FIG. 1, the rubber base material 2a side of the test piece 2 is adhered to the lower surface of the iron plate 1 with double-sided tape.
The coated film 2b side of the test piece 2 is placed on the upper surface of the glass plate 3, and a load is applied onto the iron plate 1 using the weight 4. And iron plate 1
The wire 5 fixed to the wire 5 is pulled at a speed of 1001 III/min using a Tensilon type tensile tester (not shown). At this time, the sum of the weight W1 of the small size 4, the weight W2 of the iron plate 1, and the weight W3 of the double-sided tape is 1 kg.
is set to be. Note that the upper surface of the glass plate 3 is degreased and cleaned using trichlorethylene every time a measurement is performed.

樹脂組成物の耐摩耗性は、振子型摩耗試験機(図示略)
によって行なわれ、この摩耗子として第2図に示すよう
に幅201+1、厚さ5Il1111先端の半径が10
ma+のガラス摩耗子6が使用される。上記試験機によ
り耐摩耗性試験を行なうには、まず架橋したEPDMゴ
ムシート表面を脱脂洗浄後プライマー塗布し、その上面
に樹脂組成物をコーティングして厚さ0,31IIlの
塗膜を形成したシー1−から縦150m1ll、幅10
IllIIlの試験片を用意し、この試験片の塗膜側へ
ガラスIf 社子6を押圧し荷重3kgにて往復摺動(
ストローク100mm、速度1回/5ec)させ、EP
DMゴム基材が露出するまでの11復摺動回数によって
測定される。
The abrasion resistance of the resin composition was measured using a pendulum type abrasion tester (not shown).
As shown in FIG.
A ma+ glass abrasion element 6 is used. To conduct an abrasion resistance test using the above testing machine, first, the surface of a crosslinked EPDM rubber sheet is degreased and cleaned, then a primer is applied, and then a resin composition is coated on the top surface to form a coating film with a thickness of 0.31IIl. From 1-150m1ll in length, 10 in width
Prepare a test piece of IllIIl, press the glass plate 6 against the coating side of this test piece, and slide it back and forth with a load of 3 kg (
Stroke 100mm, speed 1 time/5ec), EP
It is measured by 11 times of backward sliding until the DM rubber base material is exposed.

樹脂組成物と他部材との固着力を測定する装置は、第3
図及び第4図に示すようにガラス固定治具7と、これに
嵌合されたガラス板8と、該ガラス板8上面に載置され
る試験片9(前記試験片2と同じ)のゴム基材9a側に
両面テープにより接着される鉄板10(縦60IllI
11、横60IIllI11厚さ2IIIIll)と、
さらに前記鉄板10上面に載置されかつワイヤー11を
介して図示しないテンシロンに接続された引張用治具1
2とにJ:り構成されている。
The device for measuring the adhesion force between the resin composition and other members is the third one.
As shown in FIG. 4, the glass fixing jig 7, the glass plate 8 fitted thereto, and the rubber of the test piece 9 (same as the test piece 2) placed on the top surface of the glass plate 8. Iron plate 10 (vertical 60IllI) adhered to the base material 9a side with double-sided tape
11, width 60IIIllI11 thickness 2IIIll),
Furthermore, a tensioning jig 1 is placed on the upper surface of the iron plate 10 and connected to a tensilon (not shown) via a wire 11.
It is composed of 2 and J:ri.

上記測定装置を用いて固着力を測定するには、まず、試
験片9のゴム基材9a側を両面テープにより鉄1fii
10に接着する。そして、この試験片9の塗膜9b側を
水滴をたらしたガラス板8上面に接触さゼ、鉄板10上
に3k(lの重り(図示路)を載せる。この状態のまま
80℃の恒温槽中に1時間放置する。さらに、恒温槽か
ら取り出し室温中に30分放置した後、前記重りを取り
去り、テンシロン(図示路)によりワイヤー11を介し
て引張用活貝12を引張る。このときの最大荷重(kQ
)を固着力とする。
To measure the adhesion force using the above measuring device, first, attach the rubber base material 9a side of the test piece 9 to the iron 1fi with double-sided tape.
Glue to 10. Then, the coating film 9b side of this test piece 9 is brought into contact with the top surface of the glass plate 8 on which water droplets have been dropped, and a 3k (l weight (as shown) is placed on the iron plate 10. In this state, a constant temperature bath at 80° C. Further, after taking it out of the thermostatic chamber and leaving it at room temperature for 30 minutes, the weight is removed and the tension live shellfish 12 is pulled through the wire 11 using Tensilon (the path shown in the figure).At this time, the maximum Load (kQ
) is the adhesion force.

次に、EPDMゴム基材9aに樹脂組成物をコーティン
グして塗膜9bを形成した場合の剥離力を測定するには
、引張試験機が用いられる。この場合試験片9は#25
0IIII111横5IIImに形成され、ゴム基材9
aから塗g19bを剥離するときの剥離強度(k!I/
c+ll)を測定する。なお、前記塗膜9hが破断づる
とぎは、試験片9の塗膜9b表面に伸縮性の小さい布を
接着剤で接着し補強する。
Next, a tensile tester is used to measure the peeling force when the EPDM rubber base material 9a is coated with the resin composition to form the coating film 9b. In this case, test piece 9 is #25
0III111 horizontally 5IIIm, rubber base material 9
Peeling strength (k!I/
c+ll). In addition, when the coating film 9h is broken, a cloth with low elasticity is bonded to the surface of the coating film 9b of the test piece 9 with an adhesive to reinforce it.

さて、表1は比較例1〜3と熱可塑性ウレタンエクスト
マーをベースとする実施例1〜3の成分配合を示し、空
欄は無添加を示す。又、表2は前記比較例1〜3及び実
施例1〜3の評価結果を示す。
Now, Table 1 shows the component formulations of Comparative Examples 1 to 3 and Examples 1 to 3 based on thermoplastic urethane extomers, and blank columns indicate no addition. Moreover, Table 2 shows the evaluation results of Comparative Examples 1 to 3 and Examples 1 to 3.

表2から明らかなように、比較例1〜3はそれぞれ摩擦
係数、耐摩耗性、固着力及び剥離力の4つの性質を全て
満足しないが、実施例1〜3はそれぞれ前記4つの性質
を全て満足する。
As is clear from Table 2, Comparative Examples 1 to 3 each do not satisfy all of the four properties of friction coefficient, wear resistance, adhesion force, and peeling force, but Examples 1 to 3 each do not satisfy all of the four properties. be satisfied.

夷1 (u1位重団部) 表2 表3はポリアミドエラストマーをベースとする比93例
4〜6と実施例4〜6の成分配合を示し、又、表4はそ
れらの評価結果を示す。この表4から明らかなように、
実施例4〜6は摩擦係数、耐摩耗性、固着力及び剥離力
の4つの性質全てを満足するが、比較例4〜6はいずれ
も4つの性質全てを満足しない。
夷1 (U1-position polymer moiety) Table 2 Table 3 shows the component formulations of 93 Examples 4 to 6 and Examples 4 to 6 based on polyamide elastomer, and Table 4 shows their evaluation results. As is clear from Table 4,
Examples 4 to 6 satisfy all four properties of friction coefficient, abrasion resistance, adhesion force, and peeling force, but Comparative Examples 4 to 6 do not satisfy all four properties.

(以下余白) 表3 (11位重量部) 表4 次に、表5に示した実施例7〜10について述べると、
実施例7.8は熱可塑性ウレタンエラストマーをベース
とし、実施例9.10はナイロンエラストマーをベース
どしたbのである。又、実施例7〜10は本発明の必須
要件ではないが融点150℃以下のポリオレフィン又は
二&llI化モリブデンを添加している。前記ポリオレ
フィンに(Jポリエチレン、ポリプロピレン、それらの
共重合体及びワックス類等があり、樹脂組成物の潤δ(
性を増し、分散加工性、耐摩耗M il【びに強但を増
加させる作用がある。又、二硫化モリブデンは樹脂組成
物の潤滑性を増加する作用があるが、添加量を1〜50
重ω部にするのが望ましい。これらの実施例7〜10の
評価結果は表6に示され、前述した実施例1〜3と比較
して実施例7〜10の摩擦係数等の4つの性質が優れて
いることがわかる。
(Margins below) Table 3 (11th part by weight) Table 4 Next, Examples 7 to 10 shown in Table 5 will be described.
Examples 7.8 are based on thermoplastic urethane elastomers and Examples 9.10 are based on nylon elastomers. Further, in Examples 7 to 10, polyolefin having a melting point of 150° C. or lower or molybdenum di-II compound was added, although this was not an essential requirement of the present invention. The polyolefins include (J polyethylene, polypropylene, copolymers thereof, waxes, etc.), and the moisture content of the resin composition δ(
It has the effect of increasing dispersion processability, wear resistance, and strength. In addition, molybdenum disulfide has the effect of increasing the lubricity of the resin composition, but the amount added is 1 to 50%.
It is desirable to make it a heavy ω part. The evaluation results of Examples 7 to 10 are shown in Table 6, and it can be seen that Examples 7 to 10 are superior in four properties such as the coefficient of friction compared to Examples 1 to 3 described above.

R後に前述した各実施例1〜10に使用された各成分の
貝体例を表7に示す。
Table 7 shows shell examples of each component used in each of Examples 1 to 10 described above after R.

表5 (単位重量部) 表6 表7Table 5 (unit weight parts) Table 6 Table 7

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は摩擦係数の測定装置を示す正面図、第2図は振
子IJX!摩耗試験機に用いられるガラス摩耗子の斜視
図、第3図はv:J着力の測定装置を示す正面図、第4
図は同じく平面図である。
Figure 1 is a front view showing the friction coefficient measuring device, and Figure 2 is the pendulum IJX! FIG. 3 is a perspective view of a glass abrasion element used in an abrasion tester; FIG.
The figure is also a plan view.

Claims (1)

【特許請求の範囲】 i、1ooita部の熱可塑性エラストマーと、1〜5
0ffiia部のシリコーンオイルと、5〜200 f
fi fi1部のテフロンパウダーとにより構成したこ
とを特徴とする樹脂組成物。 2、シリコーンオイルは5〜20!ll’fi1部、テ
フロンパウダーは10〜30重量部である特許請求の範
囲第1項記載の樹脂組成物。
[Scope of Claims] i, 1 ooita part of a thermoplastic elastomer, and 1 to 5
0ffia part silicone oil and 5 to 200 f.
1 part of Teflon powder; and 1 part of Teflon powder. 2. Silicone oil is 5-20! The resin composition according to claim 1, wherein the amount of ll'fi is 1 part and the amount of Teflon powder is 10 to 30 parts by weight.
JP58184089A 1983-09-30 1983-09-30 Resin composition Granted JPS6076561A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58184089A JPS6076561A (en) 1983-09-30 1983-09-30 Resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58184089A JPS6076561A (en) 1983-09-30 1983-09-30 Resin composition

Publications (2)

Publication Number Publication Date
JPS6076561A true JPS6076561A (en) 1985-05-01
JPS6126948B2 JPS6126948B2 (en) 1986-06-23

Family

ID=16147201

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58184089A Granted JPS6076561A (en) 1983-09-30 1983-09-30 Resin composition

Country Status (1)

Country Link
JP (1) JPS6076561A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63210146A (en) * 1987-02-26 1988-08-31 Kinugawa Rubber Ind Co Ltd Surface-treating agent
JPH01197533A (en) * 1988-02-02 1989-08-09 Kinugawa Rubber Ind Co Ltd Coating composition for surface treatment of polymeric elastomer
KR100493231B1 (en) * 2002-07-23 2005-06-03 현대모비스 주식회사 The composition for improving the anti-scratching property tpu for instrument of panel
CN107636073A (en) * 2015-05-18 2018-01-26 奥伯尼国际有限责任公司 Silicone composition and fluoropolymer additive are to improving the purposes of the property of polymer composition
US10759923B2 (en) 2015-10-05 2020-09-01 Albany International Corp. Compositions and methods for improved abrasion resistance of polymeric components

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5120208A (en) * 1974-08-12 1976-02-18 Tatsuo Ikeno Anshodehatsukosuru tojishitsutairu oyobi sonotairuomochiita mozaikuban

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5120208A (en) * 1974-08-12 1976-02-18 Tatsuo Ikeno Anshodehatsukosuru tojishitsutairu oyobi sonotairuomochiita mozaikuban

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63210146A (en) * 1987-02-26 1988-08-31 Kinugawa Rubber Ind Co Ltd Surface-treating agent
JPH01197533A (en) * 1988-02-02 1989-08-09 Kinugawa Rubber Ind Co Ltd Coating composition for surface treatment of polymeric elastomer
KR100493231B1 (en) * 2002-07-23 2005-06-03 현대모비스 주식회사 The composition for improving the anti-scratching property tpu for instrument of panel
CN107636073A (en) * 2015-05-18 2018-01-26 奥伯尼国际有限责任公司 Silicone composition and fluoropolymer additive are to improving the purposes of the property of polymer composition
JP2018517030A (en) * 2015-05-18 2018-06-28 オルバニー インターナショナル コーポレイション Use of silicone-containing additives and fluoropolymer additives to improve the properties of polymer compositions
JP2021193181A (en) * 2015-05-18 2021-12-23 オルバニー インターナショナル コーポレイション Use of silicone-containing additive and fluoropolymer additive to improve properties of polymeric compositions
US10759923B2 (en) 2015-10-05 2020-09-01 Albany International Corp. Compositions and methods for improved abrasion resistance of polymeric components
US11485836B2 (en) 2015-10-05 2022-11-01 Albany International Corp. Compositions and methods for improved abrasion resistance of polymeric components

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