JPH0361798B2 - - Google Patents
Info
- Publication number
- JPH0361798B2 JPH0361798B2 JP14345583A JP14345583A JPH0361798B2 JP H0361798 B2 JPH0361798 B2 JP H0361798B2 JP 14345583 A JP14345583 A JP 14345583A JP 14345583 A JP14345583 A JP 14345583A JP H0361798 B2 JPH0361798 B2 JP H0361798B2
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- slip resistance
- weight
- parts
- cork powder
- 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
- 239000007799 cork Substances 0.000 claims description 22
- 239000000463 material Substances 0.000 claims description 22
- 239000000843 powder Substances 0.000 claims description 21
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 20
- 238000009408 flooring Methods 0.000 claims description 14
- 229920001971 elastomer Polymers 0.000 claims description 12
- 239000005060 rubber Substances 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 9
- 229920002367 Polyisobutene Polymers 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 claims description 4
- 229920002725 thermoplastic elastomer Polymers 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 description 14
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 13
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 10
- 230000000694 effects Effects 0.000 description 8
- 238000005336 cracking Methods 0.000 description 6
- 244000043261 Hevea brasiliensis Species 0.000 description 5
- 239000005062 Polybutadiene Substances 0.000 description 5
- 229920003052 natural elastomer Polymers 0.000 description 5
- 229920001194 natural rubber Polymers 0.000 description 5
- 229920002857 polybutadiene Polymers 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 229920005549 butyl rubber Polymers 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 229920003051 synthetic elastomer Polymers 0.000 description 4
- 238000004073 vulcanization Methods 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 229920001084 poly(chloroprene) Polymers 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229920006030 multiblock copolymer Polymers 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
Landscapes
- Floor Finish (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は、耐スリツプ性を高めた床材に関する
ものである。
一般に、車両や建築物などのフロアには、その
保護あるいは外観向上、保温性向上、歩行感、歩
行音の低減などという観点からゴム製の床材を設
けることが多いが、この床材に要求される特性と
して耐スリツプ性があり、この耐スリツプ性は歩
行者の安全上、床材にとつて最も重要な特性の一
つであるということができる。
従来、上記床材としては、天然ゴムまたは合成
ゴムに、充填剤として炭酸カルシウム、クレー、
顔料などを加えて圧延したものや、塩化ビニル製
のゴム状弾性を有するものなどがあるが、いずれ
も平滑な表面を有するものは耐スリツプ性が低
く、特に床面が濡れた状態にあるときにはスリツ
プし易くなるという不具合がある。因に、床材表
面に凹凸を与えて耐スリツプ性の向上を図ること
も一般には行なわれているが、凹凸が歩行に際し
て違和感を与えたり、凹部に埃等が堆積して外観
を損い易いという不具合が生じ、あまり好ましい
ものではない。
本発明は、かかる点に鑑み、ゴム状物質を主成
分とする床材において、添加材に工夫を加えるこ
とにより、床材が乾燥時および浸潤時のいずれに
おいても優れた耐スリツプ性を呈するようにな
し、歩行の安全性を確保することを目的とするも
のである。
本発明にかかる床材は、ゴム状物質、すなわ
ち、架橋可能なゴムあるいは熱可塑性のゴム状ポ
リマーあるいは上記ゴムとゴム状ポリマーとの混
合物100重量部に対し、平均粒子径が0.1〜2.0mm
のコルク粉が1〜10重量部、ポリイソブチレンあ
るいはイソブチレンを主成分とする共重合体をイ
ソブチレン量にして1〜15重量部添加したことを
特徴とするものである。
架橋可能なゴムとしては、NR(天然ゴム)、
SBR(スチレン・ブタジエンゴム)、BR(ブタジ
エンゴム)、NBR(ニトリル・ブタジエンゴム)、
CR(クロロプレンゴム)、EPR(エチレン・プロ
ピレンゴム)など硫黄、金属酸化物、過酸化物、
樹脂等の架橋剤により三次元網目鎖が形成される
ものが適用される。
熱可塑性のゴム状ポリマーとしては、スチレン
(S)とブタジエン(B)とによるSBS型テレブロツ
ク、マルチブロツク共重合体、ハイスチレンゴ
ム、1,2−ポリブタジエンなど一般に熱可塑性
エラストマーと呼ばれるものが適用される。
コルク粉としては、天然物を機械的に粉砕した
ものが適用される。しかして、このコルク粉の平
均粒子径は0.1〜2.0mmの範囲に設定されるが、そ
の理由は、平均粒子径が0.1mm未満では耐スリツ
プ性の向上が十分に図れず、また、平均粒子径が
2.0mmを越えると床材表面の平滑性が損われ、使
用中に床材表面に露出しているコルク粒子が脱離
してしまう不具合があるためである。
一方、上記平均粒子径0.1〜2.0mmのコルク粉は
ゴム状物質100重量部に対して1〜10重量部添加
されるが、その理由は、1重量部未満では耐スリ
ツプ性の向上が十分に図れず、また、10重量部を
越えると、機械的特性が低下し、歩行による表面
の荒れが生じて耐久性が低下することになるため
である。特に、10重量部を越えると耐オゾンクラ
ツク性の顕著な低下が認められる。
イソブチレン系重合体としては、ポリイソブチ
レンあるいはイソブチレンを主成分とする共重合
体、例えばイソブチレンとイソプレンとの共重合
体であるブチルゴムが適用される。
イソブチレン系重合体のイソブチレン量は、ゴ
ム状物質100重量部に対して1〜15重量部に設定
されるが、その理由は、1重量部未満では耐スリ
ツプ性の向上が充分に図れず、また、15重量部を
越えると、残留へこみ量の増大、耐スクラツチ
(引掻傷のつき難さ)および耐摩耗性の低下、表
面の汚れ易さなどを招き、耐スリツプ性以外の特
性での問題が生じて好ましくないためである。特
に、15重量部を越えた場合、残留へこみ量の顕著
な増加が認められる。上記イソブチレン量のゴム
状物質100重量部に対する望しい値は3〜10重量
部である。
もちろん、本発明にかかる床材は、上記コルク
粉およびイソブチレン系重合体以外に、補強剤、
充填剤、軟化剤、加硫剤、加硫促進剤、加硫促進
助剤など他の添加剤を必要に応じて適宜選択して
添加し得るものである。
以下、本発明の実施例を説明する。
実施例1〜5、比較例1〜9
本実施例および比較例の共通配合は第1表に示
されている。
The present invention relates to a flooring material with improved slip resistance. In general, rubber flooring is often installed on the floors of vehicles, buildings, etc. from the viewpoints of protecting the floor, improving the appearance, improving heat retention, feeling of walking, and reducing walking noise. One of the most important properties is slip resistance, and this slip resistance can be said to be one of the most important properties for flooring materials in terms of pedestrian safety. Conventionally, the above-mentioned flooring materials have been made of natural rubber or synthetic rubber with fillers such as calcium carbonate, clay, etc.
There are those that are rolled with added pigments, and those that have rubber-like elasticity made of vinyl chloride, but all of them have a smooth surface and have low slip resistance, especially when the floor is wet. There is a problem that it becomes easy to slip. Incidentally, it is common practice to improve slip resistance by adding unevenness to the surface of the flooring material, but unevenness can make it uncomfortable to walk on, and dust can accumulate in the recesses, damaging the appearance. This problem occurs and is not very desirable. In view of this, the present invention has been developed to improve the additives of flooring materials mainly composed of rubber-like substances so that the flooring materials exhibit excellent slip resistance both when dry and when soaked. The purpose is to ensure walking safety. The flooring material according to the present invention has an average particle diameter of 0.1 to 2.0 mm based on 100 parts by weight of a rubbery substance, that is, a crosslinkable rubber or a thermoplastic rubbery polymer, or a mixture of the above-mentioned rubber and rubbery polymer.
It is characterized in that 1 to 10 parts by weight of cork powder and 1 to 15 parts by weight of polyisobutylene or a copolymer containing isobutylene as a main component are added. Crosslinkable rubbers include NR (natural rubber),
SBR (styrene/butadiene rubber), BR (butadiene rubber), NBR (nitrile/butadiene rubber),
CR (chloroprene rubber), EPR (ethylene propylene rubber), etc. Sulfur, metal oxides, peroxides,
A material in which a three-dimensional network chain is formed by a crosslinking agent such as a resin is applied. As the thermoplastic rubbery polymer, what is generally called a thermoplastic elastomer is used, such as SBS type teleblock made of styrene (S) and butadiene (B), multiblock copolymer, high styrene rubber, and 1,2-polybutadiene. Ru. As the cork powder, a mechanically pulverized natural product is used. However, the average particle size of this cork powder is set in the range of 0.1 to 2.0 mm.The reason is that if the average particle size is less than 0.1 mm, the slip resistance cannot be sufficiently improved; The diameter is
This is because if it exceeds 2.0 mm, the smoothness of the flooring material surface will be impaired, and cork particles exposed on the flooring material surface will come off during use. On the other hand, cork powder with an average particle size of 0.1 to 2.0 mm is added in an amount of 1 to 10 parts by weight per 100 parts by weight of the rubbery substance.The reason is that less than 1 part by weight does not sufficiently improve slip resistance. Moreover, if the amount exceeds 10 parts by weight, the mechanical properties will deteriorate and the surface will become rough due to walking, resulting in a decrease in durability. In particular, when the amount exceeds 10 parts by weight, a remarkable decrease in ozone crack resistance is observed. As the isobutylene polymer, polyisobutylene or a copolymer containing isobutylene as a main component, such as butyl rubber, which is a copolymer of isobutylene and isoprene, is used. The amount of isobutylene in the isobutylene polymer is set at 1 to 15 parts by weight per 100 parts by weight of the rubber-like material, because if it is less than 1 part by weight, the slip resistance cannot be sufficiently improved. If the amount exceeds 15 parts by weight, the amount of residual dents will increase, the scratch resistance and abrasion resistance will decrease, and the surface will become easily stained, leading to problems with properties other than slip resistance. This is because this is not desirable. In particular, when the amount exceeds 15 parts by weight, a significant increase in the amount of residual dents is observed. The desired amount of isobutylene is 3 to 10 parts by weight based on 100 parts by weight of the rubbery material. Of course, the flooring material according to the present invention includes, in addition to the cork powder and isobutylene polymer, reinforcing agents,
Other additives such as fillers, softeners, vulcanizing agents, vulcanization accelerators, and vulcanization accelerators may be appropriately selected and added as necessary. Examples of the present invention will be described below. Examples 1 to 5, Comparative Examples 1 to 9 The common formulations of the Examples and Comparative Examples are shown in Table 1.
【表】
上表中、ハイスチレンゴムは日本合成ゴム社製
のHSR0061である。
実施例1〜5および比較例1〜9は、第1表の
配合をベースとし、コルク粉とイソブチレン系重
合体の添加量を第2表および第3表に示す如く設
定したものであり、この実施例および比較例につ
いて、耐スリツプ性、オゾン亀裂発生の有無、残
留へこみに関する試験を行なつた。試験結果は第
2表および第3表に示されている。[Table] In the above table, the high styrene rubber is HSR0061 manufactured by Japan Synthetic Rubber Co., Ltd. Examples 1 to 5 and Comparative Examples 1 to 9 were based on the formulations in Table 1, and the amounts of cork powder and isobutylene polymer added were set as shown in Tables 2 and 3. The Examples and Comparative Examples were tested for slip resistance, presence or absence of ozone cracking, and residual dents. The test results are shown in Tables 2 and 3.
【表】【table】
【表】
なお、コルク粉の平均粒子径はいずれの例も
0.9mmである。供試材の作成にあたつて、イソブ
チレン系重合体はゴム状物質と同時に、また、コ
ルク粉は他の添加物とともに密閉式混合機に投入
して混練し、この混練物を3.0mm厚のシートにし
てプレスにて加圧、加熱成形した。加硫にあたつ
ては、温度160℃で、〔レオメータ曲線の90%加硫
時間+5分〕のプレスを行なつた。すべり抵抗係
数Dの測定はJISA1407振子形すべり抵抗試験機
により、また、オゾン亀裂発生試験はオゾン濃度
50pphm、1%伸長、試験時間24時間という条件
で、さらに、残留へこみの測定はJISA−1407に
基いてそれぞれ行なつた。第2表中、ビスタネツ
クMML−80はエクソン化学社製のポリイソブチ
レンであり、また、第3表中、ブチルゴムは日本
合成ゴム社製のブチル268である。
上記第2表から、コルク粉の添加およびイソブ
チレン系重合体の添加のいずれも各々単独で耐ス
リツプ性向上に寄与するということがわかる。コ
ルク粉を添加した場合、床材はコルク粉が存在す
る部分とそうでないゴム質部分とでモジユラスが
異るため、履物底部から力を受けた際に応力が不
均一となり、履物底部の凹凸と相俟つて見かけの
摩擦係数が高められる。つまり、コルク粉は、床
材が履物底部で力を受けた際に床材表面に凹凸模
様が存在するのと同様の効果を生み出す作用を呈
するものと認められる。一方、イソブチレン系重
合体は、床材が履物底部から受ける衝撃的エネル
ギーを吸収緩和し、反撥エネルギーによるスリツ
プ現象を抑える作用を呈するものと認められる。
しかして、コルク粉のみを添加した場合は、比
較例5、7、9で認められる如く、オゾン亀裂の
発生がみられ、このオゾン亀裂発生までの時間は
コルク粉の添加量が多くなるにつれて短くなる傾
向にあつた。一方、イソブチレン系重合体のみを
添加した場合は、比較例4、6、8で認められる
如く、その添加量の増大に伴つて残留へこみが大
きくなる傾向にある。
これに対し、実施例においては、耐スリツプ性
の向上と合わせてオゾン亀裂発生の防止と残留へ
こみの低減が図れた。これは、例えば、実施例3
と比較例4のデータを比較してわかるように、コ
ルク粉の添加が耐スリツプ性向上のみならず、残
留へこみの低減にも寄与し、また、実施例4と比
較例7のデータを比較してわかるように、イソブ
チレン系重合体の添加がオゾン亀裂発生の防止に
寄与しているためである。
すなわち、実施例においては、コルク粉の有す
る耐スリツプ性向上作用および残留へこみ低減作
用と、イソブチレン系重合体の有する耐スリツプ
性向上作用およびオゾン亀裂防止作用とが相俟つ
て、耐スリツプ性の機械的特性の双方を満足し得
る特性を呈しているものと認められる。
また、実施例5はイソブチレン系重合体として
ポリイソブチレンに代えてブチルゴムを適用した
ものであるが、実施例3のデータと比較してわか
るように、ブチルゴムの方がポリイソブチレンに
比べて耐スリツプ性向上への寄与は若干低いもの
の、残留へこみについては良好な値を有する。
実施例6〜9、比較例10〜17
本例は、ゴム状物質に先の実施例のものと異な
るものを適用して耐スリツプ性、オゾン亀裂発生
の有無、残留へこみを調べてみたものである。実
施例の配合は第4表に、比較例の配合は第5表に
それぞれ記載され、実施例の試験結果は第6表
に、比較例の試験結果は第7表にそれぞれ記載さ
れている。[Table] In addition, the average particle size of cork powder is
It is 0.9mm. To prepare the test materials, the isobutylene polymer was mixed with the rubber-like substance, and the cork powder was mixed with other additives in an internal mixer. It was made into a sheet and was pressurized and heated using a press. For vulcanization, pressing was carried out at a temperature of 160°C for [vulcanization time of 90% of the rheometer curve + 5 minutes]. The slip resistance coefficient D was measured using a JISA1407 pendulum slip resistance tester, and the ozone crack generation test was performed using an ozone concentration test.
Further, residual dents were measured based on JISA-1407 under the conditions of 50 pphm, 1% elongation, and 24 hours test time. In Table 2, Vistanec MML-80 is polyisobutylene manufactured by Exxon Chemical Co., Ltd., and in Table 3, butyl rubber is Butyl 268 manufactured by Japan Synthetic Rubber Company. From Table 2 above, it can be seen that both the addition of cork powder and the addition of isobutylene polymer independently contribute to improving the slip resistance. When cork powder is added, the modulus of the floor material differs between the part where cork powder is present and the rubbery part where it is not, so when force is applied from the sole of the footwear, the stress becomes uneven, causing unevenness on the sole of the footwear. Combined with this, the apparent coefficient of friction is increased. In other words, cork powder is recognized to have the effect of producing an effect similar to the presence of an uneven pattern on the surface of a flooring material when the flooring material receives force from the sole of footwear. On the other hand, isobutylene-based polymers are recognized to have the effect of absorbing and alleviating the impact energy that the floor material receives from the sole of the footwear, and suppressing the slip phenomenon caused by the repulsive energy. However, when only cork powder is added, ozone cracks occur as seen in Comparative Examples 5, 7, and 9, and the time until the ozone cracks occur becomes shorter as the amount of cork powder added increases. There was a tendency to On the other hand, when only the isobutylene polymer is added, as seen in Comparative Examples 4, 6, and 8, the residual dents tend to become larger as the amount added increases. On the other hand, in the examples, it was possible to prevent ozone cracking and reduce residual dents, as well as improve slip resistance. This is, for example, Example 3
As can be seen by comparing the data of Example 4 and Comparative Example 4, the addition of cork powder not only improves slip resistance but also contributes to reducing residual dents. As can be seen, this is because the addition of isobutylene-based polymers contributes to the prevention of ozone cracking. In other words, in the examples, the slip resistance improving effect and residual dent reduction effect of the cork powder, and the slip resistance improving effect and ozone crack prevention effect of the isobutylene polymer combine to create a slip resistant machine. It is recognized that the product exhibits characteristics that can satisfy both of the above-mentioned characteristics. In addition, in Example 5, butyl rubber was used instead of polyisobutylene as the isobutylene-based polymer, but as can be seen by comparing the data with Example 3, butyl rubber has better slip resistance than polyisobutylene. Although the contribution to improvement is somewhat low, it has a good value for residual dents. Examples 6 to 9, Comparative Examples 10 to 17 In this example, slip resistance, occurrence of ozone cracking, and residual denting were investigated using rubber-like materials different from those of the previous examples. be. The formulations of Examples are listed in Table 4, the formulations of Comparative Examples are listed in Table 5, the test results of Examples are listed in Table 6, and the test results of Comparative Examples are listed in Table 7.
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】
上記第4表および第5表において、NBR
N230S、BR01、RB820、HSR0061はいずれも日
本合成ゴム社製のものである。また、コルク粉の
平均粒子径はいずれも0.9mmである。
第4表と第6表から、いずれのゴム状物質を用
いた場合でもコルク粉とイソブチレン系重合体の
添加により、オゾン亀裂発生や残留へこみの問題
を生じることなく、耐スリツプ性の向上が図れ、
また、実施例6、8のように天然ゴムとハイスチ
レンゴムとの組合せ、あるいは、天然ゴム、ハイ
スチレンゴムおよびブタジエンゴムの組合せにお
いて比較的良好な耐スリツプ性が得られることが
わかる。
また、第5表と第7表から、イソブチレン系重
合体と残留へこみとの関係およびコルク粉とオゾ
ン亀裂との関係がそれぞれ明確に認識でき、かか
る関係はいずれのゴム状物質においてもみられる
ことがわかる。
以上のように、本発明によれば、ゴム状物質に
対し、平均粒子径0.1〜2.0mmのコルク粉とイソブ
チレン系重合体とをそれぞれ適量添加する構成と
したから、オゾン亀裂発生および残留へこみの増
大を招くことなく、つまり、耐候性および機械的
特性を犠牲にすることなく、耐スリツプ性の向上
が図れるという優れた効果が得られる。[Table] In Tables 4 and 5 above, NBR
N230S, BR01, RB820, and HSR0061 are all manufactured by Japan Synthetic Rubber Co., Ltd. Furthermore, the average particle diameter of the cork powder was 0.9 mm. Tables 4 and 6 show that no matter which rubbery material is used, the addition of cork powder and isobutylene polymer can improve slip resistance without causing ozone cracking or residual denting problems. ,
It is also seen that relatively good slip resistance can be obtained in the combination of natural rubber and high styrene rubber, or in the combination of natural rubber, high styrene rubber and butadiene rubber, as in Examples 6 and 8. Furthermore, from Tables 5 and 7, the relationship between isobutylene-based polymers and residual dents and the relationship between cork powder and ozone cracks can be clearly recognized, respectively, and such relationships can be seen in any rubbery substance. Recognize. As described above, according to the present invention, cork powder with an average particle size of 0.1 to 2.0 mm and isobutylene polymer are added in appropriate amounts to the rubber-like material, thereby preventing ozone cracking and residual dents. An excellent effect can be obtained in that slip resistance can be improved without increasing the slip resistance, that is, without sacrificing weather resistance and mechanical properties.
Claims (1)
リマーあるいは上記ゴムとゴム状ポリマーとの混
合物100重量部に対し、平均粒子径が0.1〜2.0mm
のコルク粉が1〜10重量部、ポリイソブチレンあ
るいはイソブチレンを主成分とする共重合体がイ
ソブチレン量にして1〜15重量部添加されている
ことを特徴とする床材。1. Average particle size is 0.1 to 2.0 mm based on 100 parts by weight of crosslinkable rubber, thermoplastic rubbery polymer, or mixture of the above rubber and rubbery polymer.
1. A flooring material containing 1 to 10 parts by weight of cork powder and 1 to 15 parts by weight of polyisobutylene or a copolymer containing isobutylene as a main component.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14345583A JPS6034681A (en) | 1983-08-04 | 1983-08-04 | flooring |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14345583A JPS6034681A (en) | 1983-08-04 | 1983-08-04 | flooring |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6034681A JPS6034681A (en) | 1985-02-22 |
| JPH0361798B2 true JPH0361798B2 (en) | 1991-09-20 |
Family
ID=15339099
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14345583A Granted JPS6034681A (en) | 1983-08-04 | 1983-08-04 | flooring |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6034681A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2514967Y2 (en) * | 1990-06-11 | 1996-10-23 | 株式会社田島製作所 | Long, small tape measure case |
| GB9123107D0 (en) * | 1991-10-31 | 1991-12-18 | The Technology Partnership Ltd | Conformable underfoot pad |
| GB2268872A (en) * | 1991-10-31 | 1994-01-26 | The Technology Partnership Ltd | Deformable materials and structures comprising the same |
-
1983
- 1983-08-04 JP JP14345583A patent/JPS6034681A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6034681A (en) | 1985-02-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2019089911A (en) | Rubber composition for tire and tire | |
| EP0819731B1 (en) | Diene rubber composition | |
| JPH1160810A (en) | Heavy duty pneumatic tires | |
| JPWO1996030444A1 (en) | Diene-based rubber composition | |
| JP7566782B2 (en) | Rubber composition and tire | |
| JP4275388B2 (en) | Tread rubber composition and tire | |
| JP7348840B2 (en) | Rubber composition for prosthetic soles and prosthetic soles | |
| JP4280804B2 (en) | Filled halobutyl elastomer composition | |
| JPS586738B2 (en) | High hardness rubber composition | |
| JPS62112640A (en) | Rubber composition for tire tread | |
| JP2008524342A (en) | Elastomer composition with silica filler | |
| JPH0361798B2 (en) | ||
| JP6329003B2 (en) | Rubber composition and tire using the same | |
| JP6862894B2 (en) | Rubber composition for tires | |
| JP5479015B2 (en) | Rubber composition for tire tread and pneumatic tire | |
| JP4336096B2 (en) | Filled butyl elastomer composition having improved scorch safety and method for producing the same | |
| KR101156575B1 (en) | Composition for outsole and outsole manufactured by using the same | |
| JPH0361797B2 (en) | ||
| JP2016030789A (en) | Pneumatic tire | |
| JPH0361799B2 (en) | ||
| JP2957480B2 (en) | Shoe outsole | |
| JP3646956B2 (en) | Industrial filling tire | |
| US6852785B1 (en) | Vulcanizable elastomeric compositions for use as tire treads | |
| KR102308108B1 (en) | Wood-plastic composite | |
| JPS60197751A (en) | Rubber composition for tire tread |