JPS6126948B2 - - Google Patents
Info
- Publication number
- JPS6126948B2 JPS6126948B2 JP58184089A JP18408983A JPS6126948B2 JP S6126948 B2 JPS6126948 B2 JP S6126948B2 JP 58184089 A JP58184089 A JP 58184089A JP 18408983 A JP18408983 A JP 18408983A JP S6126948 B2 JPS6126948 B2 JP S6126948B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- examples
- resin composition
- glass
- 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
- 239000011342 resin composition Substances 0.000 claims description 16
- 238000002844 melting Methods 0.000 claims description 6
- 230000008018 melting Effects 0.000 claims description 5
- 229920000098 polyolefin Polymers 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- 229920002545 silicone oil Polymers 0.000 claims description 4
- 229920002725 thermoplastic elastomer Polymers 0.000 claims description 4
- 229920001971 elastomer Polymers 0.000 description 15
- 239000011521 glass Substances 0.000 description 15
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 14
- 238000012360 testing method Methods 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 12
- 238000000576 coating method Methods 0.000 description 12
- 238000005299 abrasion Methods 0.000 description 11
- 239000005060 rubber Substances 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 7
- 229910052742 iron Inorganic materials 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 239000000806 elastomer Substances 0.000 description 5
- 229920002943 EPDM rubber Polymers 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 2
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 229920001634 Copolyester Polymers 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000002221 fluorine Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000007779 soft material Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
Description
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
の自動車用ウエザーストリツプは、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、ウレタン系塗料やシリコ
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、
従つ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なかつた。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テイングすることによつ
て、処理工程が簡略化されたが、いずれの場合に
も前述した摩擦係数、耐摩耗性及び固着力の全て
を満足するに至らなかつた。
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
のであつて、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。
発明の構成
本発明は上記目的を達成するため、100重量部
の熱可塑性エラストマーと、5〜20重量部のシリ
コーンオイルと、10〜50重量部のふつ素樹脂パウ
ダーと、融点150℃以下の10〜100重量部の低融点
ポリオレフインとにより樹脂組成物を構成してい
る。
そこで、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。
本発明の樹脂組成物の主成分である熱可塑性エ
ラストマーには、スチレン系、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。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きく耐摩耗性
の低下を防ぐ。
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5重量部以下では潤滑性か悪く、
20重量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。
同様に、ふつ素樹脂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、100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、このふつ素樹脂パウダーはゴ
ム、樹脂あるいは金属等の異種物質にコーテイン
グ又はインサート成型する際、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(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)を向上する作用がある。
さらに、低融点ポリオレフインにはポリエチレ
ン、ポリプロピレン、それらの共重合体及びワツ
クス類等があり、樹脂組成物の潤滑性を増し、分
散加工性、耐摩耗性、ゴムに対する密着力並びに
強度を増加させる作用がある。この低融点ポリオ
レフインは融点が150℃以下のものを10〜100重量
部使用する。
発明の効果
以上4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1〜8)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。従つて、例えばグラスラン、グラスア
ウター等の自動車用ウエザーストリツプに好適で
ある。
実施例
次に、本発明の実施例を説明するが、その前に
摩擦係数、耐摩耗性、固着力及びゴムに塗布した
場合の剥離力(密着力)の測定方法について説明
する。
まず、摩擦係数の測定は、厚さ2mmのEPDMゴ
ム基材2aの表面に対し樹脂組成物をコーテイン
グして厚さ0.3mmの塗膜2bを形成したシートか
ら一辺が50mmの正方形をなす試験片2を用意す
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によつて鉄板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
100mmの速度で引張つて測定される。このとき、
重り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。
樹脂組成物の耐摩耗性は、振子型摩耗試験機
(図示略)によつて行なわれ、この摩耗子として
第2図に示すように幅20mm、厚さ5mm、先端の半
径が10mm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イング
して厚さ0.3mmの塗膜を形成したシートから縦150
mm、幅10mmの試験片を用意し、この試験片の塗膜
側へガラス摩耗子6を押圧し荷重3Kgにて往復摺
動(ストローク100mm、速度1回/sec)させ、
EPDMゴム基材が露出するまでの往復摺動回数に
よつて測定される。
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60mm、横60mm、厚さ2mm)
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12とにより構成されている。
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
より鉄板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
接触させ、鉄板10上に3Kgの重り(図示略)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空温中に
30分放置した後、前記重りを取り去り、テンシロ
ン(図示略)によりワイヤー11を介して引張用
治具12を引張る。このときの最大荷重(Kg)を
固着力とする。
次に、EPDMゴム基材9aに樹脂組成物をコー
テイングして塗膜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は縦50mm、横5mmに形成され、ゴム基
材9aから塗膜9bを剥離するときの剥離強度
(Kg/cm)を測定する。なお、前記塗膜9bが破断
するときは、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。
さて、表1は比較例1〜4と熱可塑性ウレタン
エラストマーをベースとする実施例1〜2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1〜4及び実施例1、2の評価結果を示
す。
表2から明らかなように、比較例1〜4はとも
に摩擦係数、耐摩耗性、固着力及び剥離力の4つ
の性質のいずれかを満足しないが、実施例1、2
はともに前記4つの性質を全て満足する。
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. Prior Art In general, automotive weather strips such as glass run or glass outer are made of rubber or soft material.
The material is PVC etc. 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,
Surface treatments such as flocking with short nylon fibers and painting with urethane paint, silicone paint, etc. are performed.
However, these have complicated treatment processes and high equipment costs.
Therefore, manufacturing costs are high, and sufficient product performance cannot always be obtained. Therefore, instead of flocking or painting, the treatment process has been simplified by coating with a resin composition such as polyethylene or thermoplastic urethane. The adhesion force was not completely satisfied. Purpose of the Invention The present invention has been made to eliminate the above-mentioned defects, and its purpose is to provide a resin composition that has a small coefficient of friction, excellent wear resistance, and has a small adhesion force to other members. It is in. Composition of the Invention In order to achieve the above object, the present invention comprises 100 parts by weight of a thermoplastic elastomer, 5 to 20 parts by weight of silicone oil, 10 to 50 parts by weight of fluororesin powder, and ~100 parts by weight of low melting point polyolefin constitutes the resin composition. Therefore, the characteristics, blending amount, etc. of each of the above-mentioned components will be explained. The thermoplastic elastomer 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. The elastomer provides good sealing properties with the mating member due to its appropriate flexibility, and is highly effective as a binder for each component to prevent deterioration in wear resistance. Furthermore, silicone oil has the effect of increasing the lubricity of the resin composition and lowering the coefficient of friction. This silicone oil has poor lubricity when it is less than 5 parts by weight.
If it exceeds 20 parts by weight, workability will decrease, so 5 to 20 parts by weight
Parts by weight are preferred. Similarly, fluorine resin powder also improves lubricity,
Reduces the coefficient of friction. If the amount is less than 5 parts by weight, the effect will be small, and if it is more than 100 parts by weight, the mechanical strength will be significantly lowered, resulting in a problem, so 10 to 50 parts by weight is desirable. Furthermore, when this fluorine resin powder is coated or insert molded onto a different material such as rubber, resin, or metal, it reduces the surface free energy of the resin composition (reduces the surface tension) in the molten state. It has the effect of biting into the surface better and improving adhesion (adhesion). Furthermore, low-melting point polyolefins include polyethylene, polypropylene, copolymers thereof, waxes, etc., and they have the effect of increasing the lubricity of the resin composition, dispersion processability, abrasion resistance, adhesion to rubber, and strength. There is. 10 to 100 parts by weight of this low melting point polyolefin having a melting point of 150° C. or lower is used. Effects of the Invention As is clear from the evaluation results of Examples described below, the resin composition of the present invention, which is composed of the above four components, has a lower friction coefficient and wear resistance compared to the conventional ones (Comparative Examples 1 to 8). It has excellent properties, 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 automotive weather strips such as glass runs and glass outerwear. Examples Next, examples of the present invention will be described, but before that, methods for measuring friction coefficient, abrasion resistance, adhesion force, and peeling force (adhesion force) when applied to rubber will be explained. First, the coefficient of friction was measured using a test piece with a square shape of 50 mm on one side, which was prepared by coating the surface of an EPDM rubber base material 2a with a thickness of 2 mm with a resin composition to form a coating film 2b with a thickness of 0.3 mm. Prepare 2. Then, as shown in FIG. 1, the rubber base material 2a side of the test piece 2 is adhered to the bottom surface of the iron plate 1 with double-sided tape, and the coating film 2b side of the test piece 2 is placed on the top surface of the glass plate 3. A load is applied onto the iron plate 1 using the weight 4. Then, the wire 5 fixed to the iron plate 1 is tested every minute by a Tensilon type tensile tester (not shown).
Measured by pulling at a speed of 100 mm. At this time,
The weight is set so that the sum of the weight W1 of the weight 4, the weight W2 of the iron plate 1, and the weight W3 of the double-sided tape is 1 kg. Note that the upper surface of the glass plate 3 is degreased and cleaned using trichlorethylene every time a measurement is performed. The abrasion resistance of the resin composition was tested using a pendulum type abrasion tester (not shown), and the abrasion element was a glass abrasion element with a width of 20 mm, a thickness of 5 mm, and a tip radius of 10 mm, as shown in Figure 2. Child 6 is used. To perform 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 0.3 mm thick coating film. Height 150
Prepare a test piece with a width of 10 mm and a glass abrasion element 6 pressed against the coating side of this test piece and slide it back and forth with a load of 3 kg (stroke 100 mm, speed 1 time/sec).
It is measured by the number of times the EPDM rubber substrate is slid back and forth until it is exposed. As shown in FIGS. 3 and 4, the device for measuring the adhesion force between the resin composition and other members includes a glass fixing jig 7, a glass plate 8 fitted to the jig 7, and an upper surface of the glass plate 8. Test piece 9 (the test piece 2
A steel plate 10 (60 mm long, 60 mm wide, 2 mm thick) is attached to the rubber base material 9a side of the rubber base material 9a (same as ) with double-sided tape.
and a tensioning jig 12 placed on the upper surface of the iron plate 10 and connected to a tensilon (not shown) via a wire 11. To measure the adhesion force using the above measuring device,
First, the rubber base material 9a side of the test piece 9 is adhered to the iron plate 10 using double-sided tape. And this test piece 9
The coating film 9b side was brought into contact with the top surface of the glass plate 8 on which water droplets were dripped, and a 3 kg weight (not shown) was placed on the iron plate 10. Leave this state in a constant temperature bath at 80°C for 1 hour. Furthermore, take it out of the thermostatic chamber and let it cool in the air.
After leaving it for 30 minutes, the weight was removed and the tensioning jig 12 was pulled through the wire 11 using a tensilon (not shown). The maximum load (Kg) at this time is taken as the fixing force. Next, a tensile tester is used to measure the peeling force when coating the resin composition on the EPDM rubber base material 9a to form the coating film 9b. In this case, the test piece 9 is formed to have a length of 50 mm and a width of 5 mm, and the peel strength (Kg/cm) when the coating film 9b is peeled off from the rubber base material 9a is measured. In addition, when the coating film 9b breaks, 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. Now, Table 1 shows the component formulations of Comparative Examples 1 to 4 and Examples 1 to 2 based on thermoplastic urethane elastomers, and blank columns indicate no addition. Table 2 shows the evaluation results of Comparative Examples 1 to 4 and Examples 1 and 2. As is clear from Table 2, Comparative Examples 1 to 4 do not satisfy any of the four properties of friction coefficient, wear resistance, adhesion force, and peeling force, but Examples 1 and 2
Both satisfy all of the above four properties.
【表】【table】
【表】
表3はポリアミドエラストマーをベースとする
比較例5〜8と実施例3、4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3、4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5〜8はこれらの性質のいずれ
かを満足しない。[Table] Table 3 shows the component formulations of Comparative Examples 5 to 8 and Examples 3 and 4 based on polyamide elastomer,
Table 4 shows the evaluation results. As is clear from Table 4, Examples 3 and 4 satisfy all four properties of friction coefficient, wear resistance, adhesion force, and peeling force, but Comparative Examples 5 to 8 satisfy any of these properties. Not satisfied.
【表】【table】
【表】
次に、表5に示した実施例5〜8について述べ
ると、実施例5、6は熱可塑性ウレタンエラスト
マーをベースとし、実施例7、8はナイロンエラ
ストマーをベースとしたものである。又、実施例
5〜8は本発明の必須要件ではないが、二硫化モ
リブデンを添加している。この二硫化モリブデン
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重量部にするのが望ましい。これ
らの実施例5〜8の評価結果は表6に示され、前
述した実施例1、3と比較して摩擦係数、固着力
がさらに向上することがわかる。
最後に、前述した各実施例1〜8に使用された
各成分の具体例を表7に示す。[Table] Next, Examples 5 to 8 shown in Table 5 will be described. Examples 5 and 6 are based on thermoplastic urethane elastomer, and Examples 7 and 8 are based on nylon elastomer. Further, in Examples 5 to 8, molybdenum disulfide was added, although it is not an essential requirement of the present invention. This molybdenum disulfide has the effect of increasing the lubricity of the resin composition, but
It is desirable that the amount added be 1 to 50 parts by weight. The evaluation results of these Examples 5 to 8 are shown in Table 6, and it can be seen that the friction coefficient and adhesion force are further improved compared to Examples 1 and 3 described above. Finally, Table 7 shows specific examples of each component used in each of Examples 1 to 8 described above.
【表】【table】
【表】【table】
【表】【table】
第1図は摩擦係数の測定装置を示す正面図、第
2図は振子型摩耗試験機に用いられるガラス摩耗
子の斜視図、第3図は固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。
Fig. 1 is a front view showing the friction coefficient measuring device, Fig. 2 is a perspective view of a glass abrasion element used in a pendulum type abrasion tester, Fig. 3 is a front view showing the adhesion force measuring device, Fig. 4 is also a plan view.
Claims (1)
20重量部のシリコーンオイルと、10〜50重量部の
ふつ素樹脂パウダーと、融点150℃以下の10〜100
重量部の低融点ポリオレフインとにより構成した
ことを特徴とする樹脂組成物。1 100 parts by weight of thermoplastic elastomer, and 5 to 100 parts by weight of thermoplastic elastomer
20 parts by weight of silicone oil, 10 to 50 parts by weight of fluororesin powder, and 10 to 100 parts by weight of melting point 150℃ or less
1. A resin composition comprising: parts by weight of a low melting point polyolefin.
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 JPS6076561A (en) | 1985-05-01 |
JPS6126948B2 true 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) |
Families Citing this family (5)
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 |
TWI774642B (en) * | 2015-05-18 | 2022-08-21 | 美商阿爾巴尼國際公司 | Use of silicone content and fluoropolymer additives to improve properties of polymeric compositions |
PL3359597T3 (en) | 2015-10-05 | 2020-07-27 | Albany International Corp. | Compositions and methods for improved abrasion resistance of polymeric components |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5120208A (en) * | 1974-08-12 | 1976-02-18 | Tatsuo Ikeno | Anshodehatsukosuru tojishitsutairu oyobi sonotairuomochiita mozaikuban |
-
1983
- 1983-09-30 JP JP58184089A patent/JPS6076561A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5120208A (en) * | 1974-08-12 | 1976-02-18 | Tatsuo Ikeno | Anshodehatsukosuru tojishitsutairu oyobi sonotairuomochiita mozaikuban |
Also Published As
Publication number | Publication date |
---|---|
JPS6076561A (en) | 1985-05-01 |
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