JPS581141B2 - Chlorosulfonated polyethylene rubber composition - Google Patents
Chlorosulfonated polyethylene rubber compositionInfo
- Publication number
- JPS581141B2 JPS581141B2 JP6367380A JP6367380A JPS581141B2 JP S581141 B2 JPS581141 B2 JP S581141B2 JP 6367380 A JP6367380 A JP 6367380A JP 6367380 A JP6367380 A JP 6367380A JP S581141 B2 JPS581141 B2 JP S581141B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- rubber
- rubber composition
- softener
- gloss
- 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
- 229920001971 elastomer Polymers 0.000 title claims description 36
- 239000005060 rubber Substances 0.000 title claims description 36
- 239000000203 mixture Substances 0.000 title claims description 16
- 229920002681 hypalon Polymers 0.000 title claims description 12
- 239000004927 clay Substances 0.000 claims description 8
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 claims description 6
- 239000001095 magnesium carbonate Substances 0.000 claims description 6
- 229910000021 magnesium carbonate Inorganic materials 0.000 claims description 6
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 6
- 229920001223 polyethylene glycol Polymers 0.000 claims description 6
- 239000002202 Polyethylene glycol Substances 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 3
- 230000008878 coupling Effects 0.000 claims description 3
- 238000010168 coupling process Methods 0.000 claims description 3
- 238000005859 coupling reaction Methods 0.000 claims description 3
- 239000003431 cross linking reagent Substances 0.000 claims description 3
- 229910000077 silane Inorganic materials 0.000 claims description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 238000004073 vulcanization Methods 0.000 description 7
- 238000000465 moulding Methods 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 239000004709 Chlorinated polyethylene Substances 0.000 description 3
- 239000006087 Silane Coupling Agent Substances 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 description 1
- OSNILPMOSNGHLC-UHFFFAOYSA-N 1-[4-methoxy-3-(piperidin-1-ylmethyl)phenyl]ethanone Chemical compound COC1=CC=C(C(C)=O)C=C1CN1CCCCC1 OSNILPMOSNGHLC-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 241000156978 Erebia Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229920006235 chlorinated polyethylene elastomer Polymers 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000005439 maleimidyl group Chemical class C1(C=CC(N1*)=O)=O 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- -1 watching red Chemical compound 0.000 description 1
Landscapes
- Escalators And Moving Walkways (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】
本発明は、加流又は架橋後の表面光沢が良好で、しかも
耐久性に優れたクロロスルホン化ポリエチレンゴム組成
物に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a chlorosulfonated polyethylene rubber composition that has good surface gloss after hot-flowing or crosslinking and has excellent durability.
一般にエスカレーターハンドレールは、第1図に示すよ
うに鋼線1を埋設した断面C型の帆布心2上に化粧ゴム
層3を加流又は架橋接着させて構成されている。Generally, an escalator handrail is constructed by bonding or cross-linking a decorative rubber layer 3 onto a canvas core 2 having a C-shaped cross section in which a steel wire 1 is embedded, as shown in FIG.
而してエスカレーターハンドレールは、デパート、スー
パーマーケット、空港その他多くの人が集まる場所に布
設されるため上記化粧ゴム層3には次のような特性が要
求されている。Since escalator handrails are installed in department stores, supermarkets, airports, and other places where many people gather, the decorative rubber layer 3 is required to have the following characteristics.
(1) 表面の光沢が良好なこと
(2) 長期にわたって使用しても光沢が損なわれない
こと
(3) 長期にわたって使用してもゴムに亀裂やへたり
が生じないこと
従来エスカレーターハンドレールの化粧ゴムとしては、
クロロスルホン化ポリエチレンゴムあるいは塩素化ポリ
エチレンゴムが使用されでいるが上記の各特性において
充分満足できるものではなかった。(1) The surface has good gloss (2) The gloss does not deteriorate even after long-term use (3) The rubber does not crack or wear out even after long-term use Cosmetics of conventional escalator handrails As rubber,
Chlorosulfonated polyethylene rubber or chlorinated polyethylene rubber has been used, but these have not been fully satisfactory in terms of the above properties.
一方、成型後化粧ゴム層表面にシリコーンオイルあるい
はポリウレタン等をコーティングし光沢を出そうとする
試みもなされているが、シリコーンオイルの場合は塗布
後すぐに光沢がなくなり、またポリウレタンの場合には
数ケ月後にひび割れが入り、かえって美感を損ねてしま
うという問題があった。On the other hand, attempts have been made to coat the surface of the decorative rubber layer with silicone oil or polyurethane after molding to make it glossy, but in the case of silicone oil, the gloss disappears immediately after application, and in the case of polyurethane, there are several There was a problem in that after a few months, cracks appeared, which actually spoiled the aesthetic appearance.
また配合面では、クロロスルホン化ポリエチレンゴムに
クレー、タルク、炭酸カルシウム等の充填剤を配合した
場合光沢が増すことが知られているが、これらのゴムで
は初期の光沢はあっても耐久性が不充分であって長期に
わたって使用した場合光沢が失なわれるという難点があ
った。In terms of formulation, it is known that when fillers such as clay, talc, and calcium carbonate are added to chlorosulfonated polyethylene rubber, the gloss increases, but even though these rubbers have initial gloss, they lack durability. There was a problem that the gloss was insufficient and the gloss was lost when used for a long period of time.
また成型時の金型表面の平滑性を向上させて光沢を増す
方法も考えられるが、このような方法で得られる光沢は
使用により短時日で失なわれてしまう。Another possible method is to improve the smoothness of the mold surface during molding to increase gloss, but the gloss obtained by such a method will be lost within a short period of time after use.
したがって表面光沢の根本的解決には、ゴム配合組成の
改善改質が必要である。Therefore, to fundamentally solve the problem of surface gloss, it is necessary to improve and modify the rubber composition.
本発明は、かかる点に対処してなされたもので、クロロ
スルホン化ポリエチレンゴム100部、シランカツプリ
ング処理ハードクレー30〜70部、炭酸マグネシウム
5〜45部、軟化剤3〜30部、ポリエチレングリコー
ル2〜10部および有効量の加流又は架橋剤から成るク
ロロスルホン化ポリエチレンゴム組成物を提供しようと
するものである。The present invention has been made to address these issues, and consists of 100 parts of chlorosulfonated polyethylene rubber, 30 to 70 parts of silane coupling-treated hard clay, 5 to 45 parts of magnesium carbonate, 3 to 30 parts of a softener, and polyethylene glycol. It is an object of the present invention to provide a chlorosulfonated polyethylene rubber composition comprising 2 to 10 parts and an effective amount of a copolymerizing or crosslinking agent.
本発明に使用されるクロロスルホン化ポリエチレンゴム
としては一般に市販されているものを使用することがで
き、例えばハイパロン#40、ハイパロン#40S(い
ずれも米国 イー・アイ・デュポン社商品名)等がある
。As the chlorosulfonated polyethylene rubber used in the present invention, commercially available ones can be used, such as Hypalon #40 and Hypalon #40S (both trade names of EI DuPont, USA). .
上記ゴムには必要に応じて塩素化ポリエチレンをブレン
ドすることも可能であるが、この場合クロロスルホン化
ポリエチレンと塩素化ポリエチレンとの比率は100:
0〜70:30の範囲で行なう必要がある。It is also possible to blend chlorinated polyethylene into the above rubber if necessary, but in this case the ratio of chlorosulfonated polyethylene to chlorinated polyethylene is 100:
It is necessary to do this in the range of 0 to 70:30.
使用可能な塩素化ポリエチレンとしては、例えばエラス
レン#301、エラスレン#401(いずれも昭和電工
株式会社商品名)等がある。Examples of usable chlorinated polyethylene include ELATHLEN #301 and ELATHLEN #401 (both trade names of Showa Denko KK).
本発明においては、充填剤としてシランカツプリング剤
処理ハードクレーと炭酸マグネシウムとを併用する。In the present invention, hard clay treated with a silane coupling agent and magnesium carbonate are used together as fillers.
シランカツプリング剤処理ハードクレーは、メルカプト
シランあるいはアミノシラン処理ハードクレーが適して
いる。As the silane coupling agent-treated hard clay, mercaptosilane- or aminosilane-treated hard clay is suitable.
シランカツプリング剤処理ハードクレーの配合量はゴム
分100部に対して30〜70部が適している。The suitable amount of the silane coupling agent-treated hard clay is 30 to 70 parts per 100 parts of rubber.
ゴム分100部に対して30部未満では表面光沢の付与
が不充分であり、70部を越えるとゴムの加工性が低下
するようになるのでいずれも不適当である。If the amount is less than 30 parts per 100 parts of rubber, the imparting of surface gloss will be insufficient, and if it exceeds 70 parts, the processability of the rubber will deteriorate, so both are unsuitable.
炭酸マグネシウムは、通常の市販品を使用可能であるが
、白度94以上、吸油量130〜180のものが好適し
ている。As magnesium carbonate, ordinary commercially available products can be used, but those with a whiteness of 94 or more and an oil absorption of 130 to 180 are suitable.
炭酸マグネシウムの配合量は、ゴム分100部に対して
5〜45部の範囲が適している。The suitable amount of magnesium carbonate is in the range of 5 to 45 parts per 100 parts of rubber.
ゴム分100部に対して5部未満では表面光沢の付与が
不充分であり、逆に45部を越えると耐久性に劣るよう
になるのでいずれも不適当である。If it is less than 5 parts per 100 parts of rubber, it will not give sufficient surface gloss, and if it exceeds 45 parts, durability will be poor, so both are unsuitable.
また本発明に使用される軟化剤としては、透明もしくは
淡黄色のものが適しており、フタル酸系軟化剤、セバシ
ン酸系軟化剤、アゼライン酸系軟化剤、エポキシ系軟化
剤、リン酸系軟化剤等を使用することができる。Transparent or pale yellow softeners are suitable for use in the present invention, including phthalic acid softeners, sebacic acid softeners, azelaic acid softeners, epoxy softeners, and phosphoric acid softeners. Agents etc. can be used.
このうち特にフタル酸系軟化剤およびエポキシ系軟化剤
が本発明に好適している。Among these, phthalic acid softeners and epoxy softeners are particularly suitable for the present invention.
軟化剤の配合量は、ゴム分100部に対して3〜30部
の範囲が適している。A suitable blending amount of the softener is 3 to 30 parts per 100 parts of rubber.
ゴム分100部に対して3部未満では加工性が悪くなり
、逆に30部を越えるとゴム表面が曇りを帯びるように
なり、かつ物性が低下するようになるのでいずれも好ま
しくない。If it is less than 3 parts per 100 parts of rubber, processability will be poor, and if it exceeds 30 parts, the rubber surface will become cloudy and the physical properties will deteriorate, so both are not preferred.
本発明に使用されるポリエチレングリコールとしては、
分子量が3000以上のものが適しており、特に分子量
10000前後のものが好適している。The polyethylene glycol used in the present invention includes:
Those with a molecular weight of 3,000 or more are suitable, and those with a molecular weight of around 10,000 are particularly suitable.
ポリエチレングリコールの配合量は、ゴム分100部に
対して2〜10部の範囲が適している。The appropriate amount of polyethylene glycol is in the range of 2 to 10 parts per 100 parts of rubber.
ゴム分100部に対して2部未満では表面光沢の付与が
不充分であり、10部を越えると成型性が低下するよう
になるのでいずれも好ましくない。If the amount is less than 2 parts per 100 parts of rubber, the imparting of surface gloss will be insufficient, and if it exceeds 10 parts, the moldability will deteriorate, so both are not preferred.
また上記組成物には、含イオウ加硫促進剤、マレイミド
化合物、有機過酸化物のような公知の加硫あるいは架橋
剤の有効量が適宜配合される。Further, effective amounts of known vulcanizing or crosslinking agents such as sulfur-containing vulcanization accelerators, maleimide compounds, and organic peroxides are appropriately blended into the above composition.
なお、これらの配合成分以外に、マグネシアなどの加硫
助剤、アンテージDAH(川口化学株式会社商品名)、
ノクラツクNS#5、ノクラツクNS#6(いずれも大
内新興化学株式会社商品名)のような非汚染性の老化防
止剤、チタン白、ウオッチングレッド、ベンジジンイエ
ロー、フタロシアニングリーン、フタロシアニンブルー
、カーボンブラック、弁柄等の顔料等を必要に応じて適
宜配合することができる。In addition to these ingredients, vulcanization aids such as magnesia, Antige DAH (trade name of Kawaguchi Chemical Co., Ltd.),
Non-staining anti-aging agents such as NOKRATSUK NS#5 and NOKRATSUK NS#6 (both trade names of Ouchi Shinko Kagaku Co., Ltd.), titanium white, watching red, benzidine yellow, phthalocyanine green, phthalocyanine blue, and carbon black. , Bengara, and other pigments may be appropriately blended as required.
本発明のゴム組成物は、ミキシングロールあるいはバン
バリーミキサーを用いて常法により混合される。The rubber composition of the present invention is mixed in a conventional manner using a mixing roll or a Banbury mixer.
このようにして得られる本発明のゴム組成物は、金型に
充填し加硫又は架橋成型することにより表面光沢の優れ
た成型品を得ることができる。The rubber composition of the present invention thus obtained can be filled into a mold and vulcanized or crosslinked to give a molded product with excellent surface gloss.
更に加硫又は架橋成型後の表面光沢は下塗り成型のゴム
のハダに大きく影響を受けるが、本発明のゴム組成物は
ロール分出しおよび押出しの際の下造りハダも極めて平
滑である。Furthermore, the surface gloss after vulcanization or crosslinking molding is greatly affected by the roughness of the rubber in the undercoat molding, but the rubber composition of the present invention has extremely smooth undercoating during roll separation and extrusion.
なお、加硫又は架橋成型時の金型は、表面クロムメッキ
を施し、鏡面に仕上げることが望ましい。Note that it is desirable that the surface of the mold used for vulcanization or crosslinking molding be chromium plated to give it a mirror finish.
以下本発明の実施例について説明する。Examples of the present invention will be described below.
実施例 1〜3
第1表の配合の組成物をバンバリーミキサーを用いて1
50℃で6分間混練し、得られたゴム組成物を用いて圧
力100kg/cm2、温度150℃、加熱時間20分
間の条件で厚さ2mmの試験シートを製造した。Examples 1 to 3 The compositions shown in Table 1 were mixed using a Banbury mixer.
The rubber composition was kneaded at 50° C. for 6 minutes, and a test sheet with a thickness of 2 mm was produced using the rubber composition obtained under the conditions of a pressure of 100 kg/cm 2 , a temperature of 150° C., and a heating time of 20 minutes.
(数字は重量部を表わす)
なお、表中の配合成分はそれぞれ以下に示すものである
。(The numbers represent parts by weight) The ingredients in the table are as shown below.
マグネシア:神島化学社製
炭酸カルシウム:白石カルシウム社製
Nu Lock 321L:米国ヒューバー・コーポレ
ーション(Huber Corporat io )社
製、シランカップリング処理ハードクレー炭酸マグネシ
ウム:神島化学社製
PEG 10000:三洋化成社製、ポリエチレングリ
コール(MW=10000)促進剤22:川口化学社製
、加硫促進剤
促進剤TRA:大内新興化学社製、加硫促進剤促進剤D
M : 同 上
HVA#2:米国イー・アイ・デュポン(E.I.Du
pont)社製、加硫促進剤DOP :大八化学社製、
ジオクチルフタレートアデカサイザーO−180A:ア
デカアーガス化学社製、可塑剤得られたシートの特性は
第2表の通りであった。Magnesia: Manufactured by Kamishima Chemical Co., Ltd. Calcium carbonate: Manufactured by Shiraishi Calcium Co., Ltd. Nu Lock 321L: Manufactured by Huber Corporation, USA, hard clay treated with silane coupling Magnesium carbonate: Manufactured by Kamishima Chemical Co., Ltd. PEG 10000: Manufactured by Sanyo Chemical Co., Ltd. Polyethylene glycol (MW=10000) Accelerator 22: Kawaguchi Chemical Co., Ltd., vulcanization accelerator Accelerator TRA: Ouchi Shinko Kagaku Co., Ltd., vulcanization accelerator Accelerator D
M: Same as above HVA #2: E.I.DuPont, USA
Vulcanization accelerator DOP: manufactured by Daihachi Chemical Co., Ltd.
Dioctyl phthalate Adekasizer O-180A: manufactured by Adeka Argus Chemical Co., Ltd., plasticizer The properties of the obtained sheet were as shown in Table 2.
一方、実施例1および比較例2の組成物を用いて第1図
に示した構造のハンドレール(長さ10m)を製造し、
光沢度の経時変化を測定した。On the other hand, a handrail (length 10 m) having the structure shown in FIG. 1 was manufactured using the compositions of Example 1 and Comparative Example 2,
Changes in gloss over time were measured.
測定結果を第2図に示す。The measurement results are shown in Figure 2.
なお、光沢度はグロスメーターを用いてハンドレールの
垂直上方から測定した値である(目視観察ではほぼ60
以上で光沢があると感じられる)。The gloss level is the value measured from vertically above the handrail using a gloss meter (visual observation shows approximately 60% gloss).
This gives the impression that it is shiny).
以上の実施例からも明らかなように、本発明によれば耐
久性に優れた表面光沢を有し、しかも機械的特性におい
て従来品とそん色のない成型品を得ることができる。As is clear from the above examples, according to the present invention, it is possible to obtain a molded product that has excellent durability and surface gloss, and has mechanical properties similar to those of conventional products.
第1図はハンドレールの断面図、第2図は本発明の組成
物で化粧ゴム層を形成したハンドレールの表面光沢の経
時変化を示すグラフである。
1・・・・・・鋼線、2・・・・・・帆布心、3・・・
・・・化粧ゴム層。FIG. 1 is a cross-sectional view of a handrail, and FIG. 2 is a graph showing changes over time in surface gloss of a handrail in which a decorative rubber layer is formed using the composition of the present invention. 1... Steel wire, 2... Canvas core, 3...
...Cosmetic rubber layer.
Claims (1)
ンカツプリング処理ハードクレー30〜70部、炭酸マ
グネシウム5〜45部、軟化剤3〜30部、ポリエチレ
ングリコール2〜10部および有効量の加硫又は架橋剤
から成るクロロスルホン化ポリエチレンゴム組成物。 2 軟化剤は、フタル酸系軟化剤、セバシン酸系軟化剤
、エポキシ系軟化剤もしくはリン酸系軟化剤から成る特
許請求の範囲第1項記載のクロロスルホン化ゴム組成物
。[Claims] 1. 100 parts of chlorosulfonated polyethylene rubber, 30 to 70 parts of silane coupling treated hard clay, 5 to 45 parts of magnesium carbonate, 3 to 30 parts of a softener, 2 to 10 parts of polyethylene glycol, and an effective amount of A chlorosulfonated polyethylene rubber composition comprising a vulcanizing or crosslinking agent. 2. The chlorosulfonated rubber composition according to claim 1, wherein the softener comprises a phthalic acid softener, a sebacic acid softener, an epoxy softener, or a phosphoric acid softener.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6367380A JPS581141B2 (en) | 1980-05-14 | 1980-05-14 | Chlorosulfonated polyethylene rubber composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6367380A JPS581141B2 (en) | 1980-05-14 | 1980-05-14 | Chlorosulfonated polyethylene rubber composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56159240A JPS56159240A (en) | 1981-12-08 |
| JPS581141B2 true JPS581141B2 (en) | 1983-01-10 |
Family
ID=13236103
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6367380A Expired JPS581141B2 (en) | 1980-05-14 | 1980-05-14 | Chlorosulfonated polyethylene rubber composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS581141B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0660301B2 (en) * | 1989-05-08 | 1994-08-10 | 横浜ゴム株式会社 | Adhesive composition |
| CN104312028B (en) * | 2014-11-12 | 2016-08-17 | 天津昕中和胶业有限公司 | A kind of oil resistant chlorosulfonated polyethylene sebific duct |
| CN104877243A (en) * | 2015-05-25 | 2015-09-02 | 南洋电缆(天津)有限公司 | Low-toxicity, high-fire-retardant, and uvioresistant cable sheath and preparation method thereof |
-
1980
- 1980-05-14 JP JP6367380A patent/JPS581141B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56159240A (en) | 1981-12-08 |
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