JPH04122762A - Composition for rubberlike film - Google Patents
Composition for rubberlike filmInfo
- Publication number
- JPH04122762A JPH04122762A JP24339990A JP24339990A JPH04122762A JP H04122762 A JPH04122762 A JP H04122762A JP 24339990 A JP24339990 A JP 24339990A JP 24339990 A JP24339990 A JP 24339990A JP H04122762 A JPH04122762 A JP H04122762A
- Authority
- JP
- Japan
- Prior art keywords
- film
- resin
- styrene
- rubber
- composition
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims description 14
- -1 polyoctenylene Polymers 0.000 claims abstract description 23
- 229920005989 resin Polymers 0.000 claims abstract description 23
- 239000011347 resin Substances 0.000 claims abstract description 23
- 229920003048 styrene butadiene rubber Polymers 0.000 claims abstract description 12
- 238000002156 mixing Methods 0.000 claims description 6
- 239000011342 resin composition Substances 0.000 claims description 2
- 239000002985 plastic film Substances 0.000 abstract description 4
- 229920006255 plastic film Polymers 0.000 abstract description 4
- 229920001577 copolymer Polymers 0.000 abstract description 3
- 238000013329 compounding Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 description 11
- 229920001971 elastomer Polymers 0.000 description 8
- 239000005060 rubber Substances 0.000 description 8
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 238000004898 kneading Methods 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 238000004073 vulcanization Methods 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- URYYVOIYTNXXBN-UPHRSURJSA-N cyclooctene Chemical compound C1CCC\C=C/CC1 URYYVOIYTNXXBN-UPHRSURJSA-N 0.000 description 2
- 239000004913 cyclooctene Substances 0.000 description 2
- 239000012943 hotmelt Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004636 vulcanized rubber Substances 0.000 description 2
- ZBSGNEYIENETRW-UHFFFAOYSA-N 2,3-bis(hydroxymethyl)phenol Chemical compound OCC1=CC=CC(O)=C1CO ZBSGNEYIENETRW-UHFFFAOYSA-N 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- 229920002633 Kraton (polymer) Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000012770 industrial material Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、比較的安価でしかも非常に柔軟で風合の良い
ゴム状フィルムおよびその製造に適した樹脂組成物に関
する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a rubber-like film that is relatively inexpensive, extremely flexible and has a good texture, and a resin composition suitable for producing the same.
(従来技術および課題)
従来、ゴム状物質はその柔軟性、強靭性、風合の良さな
とが好まれて、各種工業材料部品、生活用品など非常に
広範囲に用いられている。しかし、その機械的強度を保
持するため、加硫という工程を採らねばならず、そのた
め加工方法が非常に限定されてしまい、フィルム化がで
きていない。たたし、ゴムの持つ独特の風合いを持つフ
ィルムへの要求は多く、そのためゴムラテックスのキャ
スティングフィルムなとが作り出されているが、加硫工
程を通っていないため機械的強度、残留歪みなとまた改
善すべき点が多く、更にキャスティング法のため、成形
性が悪く比較的高価なことも欠点であった。(Prior Art and Problems) Conventionally, rubber-like substances have been favored for their flexibility, toughness, and good texture, and have been used in a very wide range of products such as various industrial material parts and household goods. However, in order to maintain its mechanical strength, it must undergo a vulcanization process, which limits processing methods and prevents it from being made into a film. However, there are many demands for films with the unique texture of rubber, and for this reason, rubber latex casting films are produced, but because they have not gone through a vulcanization process, they have poor mechanical strength and residual distortion. In addition, there are many points that need to be improved, and since it is a casting method, it has poor moldability and is relatively expensive.
一方、ゴム工業ではカレンダー法により加硫ゴムシート
を製造しており、このものの風合い、機械的強度などは
満足するべきものであるが、このシートの厚みはせいぜ
い11程度で、より薄いフィルム状のものが望まれてい
た。On the other hand, in the rubber industry, vulcanized rubber sheets are manufactured by the calendar method, and although the texture and mechanical strength of these sheets are satisfactory, the thickness of these sheets is at most about 11 mm, and thinner film-like sheets are being produced. Something was desired.
本発明者らは、ゴムラテックスフィルムと同様の厚みを
持ちながら、ゴムシートと同様の風合い及び機械的強度
を持つゴム状フィルムを安価に大量生産すべく鋭意検討
した結果本発明に到達した。The present inventors have arrived at the present invention as a result of intensive studies aimed at inexpensively mass-producing a rubber-like film that has the same thickness as a rubber latex film and has the same feel and mechanical strength as a rubber sheet.
(課題を解決するための手段)
即ち本発明は、ポリオクテニレン樹脂にスチレン−ブタ
ジエン共重合体を配合してなるゴム状フィルム組成物お
よびこの組成物からなるゴム状フィルムである。(Means for Solving the Problems) That is, the present invention provides a rubbery film composition formed by blending a styrene-butadiene copolymer with a polyoctenylene resin, and a rubbery film formed from this composition.
本発明で使用されるポリオクテニレン樹脂は、シクロオ
クテンを重合してなり、炭素原子8個当たり1個の二重
結合を持ち、かつ分子量が一万以上であることか必要で
、トランス含量が50%以上、好ましくは60%以上で
、結晶化度か10%以上の範囲にあるのが好ましい。ま
たこのポリオクテニレン樹脂は、融点が通常40℃以上
、好ましくは50℃ないし60℃の範囲にあり、ガラス
転移点は一75℃ないし一30℃の範囲にあるのが好ま
しい。The polyoctenylene resin used in the present invention is made by polymerizing cyclooctene, has one double bond per 8 carbon atoms, has a molecular weight of 10,000 or more, and has a trans content of 50%. Above, it is preferably 60% or more, and the crystallinity is preferably in the range of 10% or more. Further, this polyoctenylene resin usually has a melting point of 40°C or higher, preferably in the range of 50°C to 60°C, and a glass transition point of preferably in the range of -75°C to -30°C.
このポリオクテニレン樹脂を構成する基材である、シク
ロオクテンの合成法としては、種々の方法が採用できる
が、例えばブタジェンを三量化した後、残った2個の二
重結合のうち1個を水素添加することにより得られる。Various methods can be adopted to synthesize cyclooctene, which is the base material constituting this polyoctenylene resin, but for example, after trimerizing butadiene, one of the remaining two double bonds is hydrogenated. It can be obtained by
本発明で使用されるポリオクテニレン樹脂は、そのまま
でも充分に良好な物性を有するが、過酸化物、フェノー
ル樹脂、イオウ系化合物など加硫剤、加硫促進剤として
知られる物質や、カルホシ酸またはその酸無水物を溶融
混合あるいは添加混合するのがより好ましい。Although the polyoctenylene resin used in the present invention has sufficiently good physical properties as it is, it may contain substances known as vulcanizing agents and vulcanization accelerators such as peroxides, phenolic resins, and sulfur compounds, as well as carbosic acid and its like. It is more preferable to melt mix or add and mix the acid anhydride.
本発明におけるスチレン−ブタジエン共重合体は、スチ
レンモノマーとブタジェンモノマーを所定量配合して後
重合することにより得られる。これらモノマーの重合方
法はラジカル重合、リビングアニオン重合なと種々の重
合法が利用でき、これら重合法の違いにより得られた共
重合体もランダム共重合体、ブロック共重合体なと構造
か異るが、これらは全て本発明のゴム状フィルム組成物
の成分として利用可能である。更に得られたスチレン−
ブタジエン共重合体のブタジェンセグメントの中の炭素
−炭素二重結合の一部または全部を水素添加したものも
好ましく使用可能である。The styrene-butadiene copolymer in the present invention is obtained by blending a styrene monomer and a butadiene monomer in predetermined amounts and post-polymerizing the mixture. Various polymerization methods can be used to polymerize these monomers, such as radical polymerization and living anion polymerization, and the copolymers obtained by these polymerization methods also have different structures, such as random copolymers and block copolymers. However, all of these can be used as components of the rubbery film composition of the present invention. Furthermore, the obtained styrene-
A butadiene copolymer obtained by hydrogenating some or all of the carbon-carbon double bonds in the butadiene segment can also be preferably used.
本発明におけるゴム状フィルム組成物には、染顔料、各
種安定剤、充填剤、可塑剤、酸化防止剤、紫外線吸収剤
、造核剤、帯電防止剤、難燃剤、増粘剤などを必要に応
じて添加することもてきる。The rubbery film composition of the present invention requires dyes and pigments, various stabilizers, fillers, plasticizers, antioxidants, ultraviolet absorbers, nucleating agents, antistatic agents, flame retardants, thickeners, etc. You can also add it depending on your needs.
本発明におけるポリオクテニレン樹脂とスチレン−ブタ
ジエン共重合体の混線方法としては、従来から公知の種
々の混練機が利用できる。例えばゴム用ロールを使って
もよいし、ゴム用加圧ニダーにポリオクテニレン樹脂、
スチレン−ブタジエン共重合体、加硫剤、各種添加剤な
どを、−度に仕込んで溶融混練してもよい。またこれら
原料を、あらかじめトライブレンドしておき、次いてプ
ラスチックス用押出機で溶融混練することもできる。As a method for mixing the polyoctenylene resin and styrene-butadiene copolymer in the present invention, various conventionally known kneading machines can be used. For example, you can use a rubber roll, or use a pressure kneader for rubber with polyoctenylene resin.
A styrene-butadiene copolymer, a vulcanizing agent, various additives, and the like may be charged at the same time and melt-kneaded. Alternatively, these raw materials may be triblended in advance and then melt-kneaded using an extruder for plastics.
本発明のゴム状フィルム組成物は、次いてプラスチック
ス工業において従来から公知の種々の方法により、フィ
ルム状に成形される。例えばT−ダイ法、インフレーシ
ョン法などが挙げられる。The rubbery film composition of the present invention is then formed into a film by various methods conventionally known in the plastics industry. Examples include the T-die method and the inflation method.
また本発明のゴム状フィルム組成物の各種物性を改良す
る目的で、種々のゴムあるいはプラスチックスを添加す
ることもできる。これらの添加方法としては、あらかじ
めポリオクテニレン樹脂にブレンドしておいてもよいし
、ポリオクテニレン樹脂、スチレン−ブタジエン共重合
体、加硫剤、各種添加剤などのなかにトライブレンドし
て、度に溶融混練してもよい。Furthermore, various rubbers or plastics may be added for the purpose of improving various physical properties of the rubbery film composition of the present invention. These can be added by blending them into the polyoctenylene resin in advance, or by tri-blending them into the polyoctenylene resin, styrene-butadiene copolymer, vulcanizing agent, various additives, etc., and then melt-kneading them at the same time. You may.
(発明の効果)
本発明のゴム状フィルム組成物から得られるゴム状フィ
ルムは、ゴム本来の特性である柔軟さ、強靭さ、風合い
を持ち、しかも通常のプラスチックスフィルムと同様の
厚みを持っている。しかも、このゴム状フィルム組成物
は通常のプラスチックスフィルム用成形機で簡単にフィ
ルム化可能であるため、安価で大量に製造可能である。(Effects of the Invention) The rubbery film obtained from the rubbery film composition of the present invention has the flexibility, toughness, and texture that are inherent to rubber, and has the same thickness as ordinary plastic films. There is. Furthermore, since this rubbery film composition can be easily formed into a film using a common plastic film molding machine, it can be manufactured in large quantities at low cost.
更に、このゴム状フィルムは加硫ゴムに近い低残留歪み
特性、及びポリオクテニレン樹脂に寄因するホットメル
ト接着性等をも有するため、通常のプラスチックスフィ
ルムに比べ、性能的にも価格的にも充分対抗可能なもの
である。Furthermore, this rubber-like film has low residual strain characteristics similar to those of vulcanized rubber, and hot-melt adhesive properties derived from polyoctenylene resin, so it is superior in terms of performance and price compared to ordinary plastic films. It is fully counterable.
(実施例) 次に本発明を実施例により具体的に説明する。(Example) Next, the present invention will be specifically explained using examples.
実施例1
ポリオクテニレン樹脂(Hils社製VESTENAM
ER8012)と、スチレン−ブタジエンブロック共重
合体(シェル化学社製カリフレックスTR1102)を
表1に示すたけ配合し、通常の押出機で溶融混練後ベレ
ット化した。このペレットを使い、通常のT−ダイ押出
機て厚み100μmのフィルムを成形した。このフィル
ムは柔軟で風合の良好なものであった。なお、このフィ
ルムの残留歪みをJISK6301に従って測定した結
果を表1に示す。Example 1 Polyoctenylene resin (VESTENAM manufactured by Hils)
ER8012) and a styrene-butadiene block copolymer (Califlex TR1102 manufactured by Shell Chemical Co., Ltd.) in the amounts shown in Table 1 were blended, and after melt-kneading in a conventional extruder, they were pelletized. Using this pellet, a film with a thickness of 100 μm was molded using a conventional T-die extruder. This film was flexible and had a good texture. Note that Table 1 shows the results of measuring the residual strain of this film in accordance with JIS K6301.
実施例2
ポリオクテニレン樹脂(Hiils社製VESTENA
MER8012)と、スチレン−ブタジエン共重合体(
シェル化学社製クレイトンG1652 )を表1に示す
たけ配合し、通常の押出機で溶融混練後ペレット化した
。このペレットを使い、インフレーション法で厚さ50
μmのフィルムを成形した。このフィルムは柔軟で風合
の良好なものであった。このフィルムをホットメルトシ
ーラーで接着し、J l5K6850に従い接着強度を
測定した結果を表1に示す。Example 2 Polyoctenylene resin (VESTENA manufactured by Hils)
MER8012) and styrene-butadiene copolymer (
Clayton G1652 (manufactured by Shell Chemical Co., Ltd.) was blended in the amounts shown in Table 1, and the mixture was melt-kneaded using a conventional extruder and then pelletized. Using this pellet, the thickness was 50 mm using the inflation method.
A μm film was molded. This film was flexible and had a good texture. This film was adhered with a hot melt sealer, and the adhesive strength was measured according to J15K6850. The results are shown in Table 1.
実施例3
実施例2において、ポリオクテニレン樹脂、クレイトン
01652の他に、ポリプロピレン樹脂(住友化学製H
3O1)を表1に示すたけ加えること以外は、実施例2
と全く同様にしてフィルム成形し、その接着強度を測定
した。結果を表1に示す。Example 3 In Example 2, in addition to polyoctenylene resin, Kraton 01652, polypropylene resin (H
Example 2 except that 3O1) was added in the amount shown in Table 1.
A film was formed in exactly the same manner as above, and its adhesive strength was measured. The results are shown in Table 1.
実施例4
ポリオクテニレン樹脂(Hiils社製VESTENA
MER8012)と、スチレン−ブタジエン共重合体(
アロン化成製AR750)を表1に示すだけ配合し、通
常の押出機で溶融混練後ペレット化した。このペレット
を使い、インフレーション法で厚さ50μ蒙のフィルム
を成形した。このフィルムは柔軟で風合の良好なもので
あった。このフィルムをホットメルトシーラーで接着し
、JIS K6850に従い接着強度を測定した結果を
表1に示す。Example 4 Polyoctenylene resin (VESTENA manufactured by Hils)
MER8012) and styrene-butadiene copolymer (
Aron Kasei Co., Ltd. AR750) was blended in the amount shown in Table 1, and after melt-kneading with a normal extruder, it was pelletized. Using this pellet, a film with a thickness of 50 μm was formed by an inflation method. This film was flexible and had a good texture. This film was adhered with a hot melt sealer, and the adhesive strength was measured according to JIS K6850. Table 1 shows the results.
実施例5
実施例4において、ポリオクテニレン樹脂1、スチレン
−ブタジエン共重合体(アロン化成製AR750)の他
に、ジメチロールフェノール樹脂(5P1045)を表
1に示すだけ加えること以外は実施例4と全く同様にし
てフィルムを成形し、その接着強度を測定した。−結果
を表1に示す。Example 5 Example 4 was completely the same as Example 4 except that in addition to polyoctenylene resin 1 and styrene-butadiene copolymer (AR750 manufactured by Aron Kasei Co., Ltd.), dimethylolphenol resin (5P1045) was added as shown in Table 1. A film was formed in the same manner and its adhesive strength was measured. -The results are shown in Table 1.
比較例1
実施例1において、ポリオクテニレン樹脂を配合しない
こと以外は実施例1と全く同様にしてフィルム成形を試
みた。このものはT−ダイがらの吐出ムラかひとく、安
定して良好なフィルムを得ることかできなかった。Comparative Example 1 Film molding was attempted in exactly the same manner as in Example 1 except that polyoctenylene resin was not blended. With this product, it was not possible to obtain a stable and good film due to uneven discharge due to the T-die.
比較例2
実施例2において、スチレン−ブタジエン共重合体(ク
レイトンG1652 )を配合しないこと以外は実施例
2と全く同様にしてフィルム成形した。Comparative Example 2 A film was formed in exactly the same manner as in Example 2, except that the styrene-butadiene copolymer (Krayton G1652) was not blended.
このフィルムは、感触はゴムというよりプラスチックス
に近いものであった。このフィルムの残留歪みと接着強
度を測定した結果を表1に示す。This film felt more like plastic than rubber. Table 1 shows the results of measuring the residual strain and adhesive strength of this film.
比較例3
実施例2において、ポリオクテニレン樹脂を配合しない
こと以外は実施例2と全く同様にしてフィルム成形を行
なったところ、インフレーションダイからの吐出か不安
定で、良好なフィルムが得られなかった。Comparative Example 3 In Example 2, film molding was carried out in exactly the same manner as in Example 2 except that the polyoctenylene resin was not blended, but the discharge from the inflation die was unstable and a good film could not be obtained.
比較例4
実施例4において、ポリオクテニレン樹脂を配合しない
こと以外は実施例4と全く同様にしてフィルム成形を行
なったところ、インフレーションダイからの吐出が不安
定で、良好なフィルムが得られなかった。Comparative Example 4 In Example 4, a film was formed in exactly the same manner as in Example 4 except that no polyoctenylene resin was blended. However, the discharge from the inflation die was unstable and a good film could not be obtained.
(以下余白)(Margin below)
Claims (2)
重合体を配合してなるゴム状フィルム組成物。(1) A rubbery film composition formed by blending a styrene-butadiene copolymer with a polyoctenylene resin.
ム。(2) A rubber-like film comprising the resin composition according to claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24339990A JPH04122762A (en) | 1990-09-13 | 1990-09-13 | Composition for rubberlike film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24339990A JPH04122762A (en) | 1990-09-13 | 1990-09-13 | Composition for rubberlike film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04122762A true JPH04122762A (en) | 1992-04-23 |
Family
ID=17103291
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24339990A Pending JPH04122762A (en) | 1990-09-13 | 1990-09-13 | Composition for rubberlike film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04122762A (en) |
-
1990
- 1990-09-13 JP JP24339990A patent/JPH04122762A/en active Pending
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