JPH0262142B2 - - Google Patents

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Publication number
JPH0262142B2
JPH0262142B2 JP58139263A JP13926383A JPH0262142B2 JP H0262142 B2 JPH0262142 B2 JP H0262142B2 JP 58139263 A JP58139263 A JP 58139263A JP 13926383 A JP13926383 A JP 13926383A JP H0262142 B2 JPH0262142 B2 JP H0262142B2
Authority
JP
Japan
Prior art keywords
rubber
pigment
present
rubber composition
vulcanization
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 - Lifetime
Application number
JP58139263A
Other languages
Japanese (ja)
Other versions
JPS6031542A (en
Inventor
Hachiro Hisada
Katsuya Kawakami
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.)
TOA GOMU KOGYO KK
Original Assignee
TOA GOMU KOGYO KK
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 TOA GOMU KOGYO KK filed Critical TOA GOMU KOGYO KK
Priority to JP13926383A priority Critical patent/JPS6031542A/en
Publication of JPS6031542A publication Critical patent/JPS6031542A/en
Publication of JPH0262142B2 publication Critical patent/JPH0262142B2/ja
Granted legal-status Critical Current

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  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はイオウ加硫により着色ゴム組成物を形
成するための未加硫ゴム組成物に関する。 従来黒以外の赤色、青色等に着色したゴムは、
未加硫ゴムに単に顔料等を混合して、その後加硫
して製造されている。この場合、加硫ゴム中にお
いて、顔料とゴム分子とが混合物の形をなしてい
る。しかしこのような顔料とゴム成分との混合物
が外的条件にさらされた時、水分で顔料が流れ出
たり、日光等の直射によつて顔料自体が分解した
り、ゴム分子自体の崩壊により、顔料自体の流出
が生じた。このような顔料の流出は、ゴム製品の
退色を意味する。したがつて従来において、黒以
外の着色ゴムの用途は主として室内に限られてい
た。又そのような着色ゴムは屋外に使用されたり
しても、1〜2月で交換しなければならないか、
又は退色したまま放置して使用しているのが現状
であつた。 本発明者は、ゴム分子中の二重結合または、活
性点に着目し、退色又は変色しないゴムについて
幅広い研究を行なつた結果、顔料又は染料分子を
ゴム分子に結合させたと考えられる方法によつて
退色又は変色しないゴムの開発に成功し本発明に
至つた。 本発明は、1種又はそれ以上の求電子試薬、前
記求電子試薬の作用により変性され得る基を有す
る有機顔料又は染料および無機顔料からなる群か
ら選ばれた着色剤を混入したことを特徴とする、
加硫により着色ゴム組成物を形成するための未加
硫ゴム組成物に関する。 本発明組成物を加熱した時、加硫が行なわれる
と同時に有機顔料あるいは染料に存在している極
性基又は無機顔料の金属原子がゴム分子中に存在
する活性点に結合して、退色又は変色しない着色
ゴム組成物が形成されると考えられる。 本発明において使用されるべきゴムとしては天
然ゴム(NR)および合成ゴムのようなすべての
ゴムが使用可能である。例えばスチレンブタジエ
ンゴム(SBR)、アクリロニトリルブタジエンゴ
ム(NBR)、クロロプレンゴム(CR)、ブチルゴ
ム(IIR)、ポリイソプレンゴム(IR)、ポリブタ
ジエンゴム(BR)、エチレンプロピレンゴム
(EPR)、およびエチレン−プロピレン−ジエン
三元重合体ゴム(EPDM)、クロロスルホン化ポ
リエチレン(CMS)、エチレン酢酸ビニル共重合
体(EVA)、等の合成ゴムが使用できる。 ゴム成分としては二重結合または、活性点を持
つていることが要件である。 求電子試薬は有機顔料又は染料の末端の極性基
又は無機顔料の金属原子から電子を取つて、これ
らをに荷電させる役割を果す。キノン類、四塩
化スズ、塩化アルミニウム、およびZnO、PbO等
の両性金属酸化物とそれらの金属の弱酸塩との混
合物である。特に四塩化スズ、ZnOとZnCO3との
混合物、キノン類、AlCl3が好ましい。この求電
子試薬は未加硫ゴム組成物100部に対し、0.2−20
重量部、好ましくは1−12重量部である。加硫ゴ
ム組成物の性質を害せず又は加硫中に分解するも
のであればこれらの求電子試薬をもつて多く使用
できる。 有機顔料又は染料としては求電子試薬によつて
変性され得る基を有する公知のものがすべて使用
できる。特にベンゼン核上にNH2、NO2
OCH3、OCH5、CONH2、Cl、CF3等が存在する
顔料又は染料が好ましい。 又は無機顔料はほとんどすべて金属原子を有す
るので、本発明において使用できる。例えば、亜
鉛華、アルミナ白、酸化チタン、ベンガラ、リサ
ージ、鉛丹、黄鉛、鉛白、亜鉛黄、モリブデン
赤、カドミウム黄等である。 顔料又は染料の使用量は本発明のゴム組成物か
ら形成される加硫ゴム組成物の用途による。 その他未加硫ゴム組成物には通常のゴム成分に
添加される公知の含硫黄加合物、樹脂加硫促進
剤、補強剤、軟化剤、着色剤、増量剤、老化防止
剤および、紫外線吸収剤等が添加されていても良
い。 本発明では加硫前に求電子試薬および特定な顔
料又は染料をゴム組成物に加えるので、通常条件
の加硫工程中にその顔料又は染料がゴム分子に結
合すると考えられる。 本発明の組成物を使用した場合、その顔料又は
染料分子が一部分又は全部がゴム成分に結合する
ので、従来のものより、退色又は変色が起りにく
い。又そのような顔料の作用によつて加硫ゴムの
強度がさらに増加したという特徴と有する。 以下に本発明の実施例を示す。単位は重量によ
る。 実施例 1 EPDM 100部 ステアリン酸 1〃 プロセスオイル 10〃 ケイ酸 30〃 メタアクリル酸エステル 3〃 ベンジジンエロー 1〃 ZnO 5〃 ZnCO3 5〃 イオウ 2〃 ジフエニルグアニジン 2〃 からなる未加硫ゴム組成物を175℃、10分間150
Kg/cm2の圧力で加硫した。その性質は第1表に示
す。 比較例 1 求電子試薬ZnCO3を添加せずに実施例1の操作
を繰返した。その結果を第1表に示す。 比較例 2 ベンジジンエローの代わりにカーボンブラツク
41部を使用して実施例1の操作を繰返した。その
結果は第1表に示す。 実施例 2−10 第1表に記載の成分を使用して実施例1の操作
を繰返した。その結果を第1表に示す。
The present invention relates to unvulcanized rubber compositions for forming colored rubber compositions by sulfur vulcanization. Traditionally, rubber colored in colors other than black, such as red or blue,
It is manufactured by simply mixing pigments etc. with unvulcanized rubber and then vulcanizing it. In this case, the pigment and rubber molecules are in the form of a mixture in the vulcanized rubber. However, when such a mixture of pigment and rubber components is exposed to external conditions, the pigment may flow out due to moisture, the pigment itself may decompose due to direct sunlight, or the rubber molecules themselves may disintegrate. A leak of its own occurred. Such pigment outflow means fading of the rubber product. Therefore, in the past, the use of colored rubber other than black was mainly limited to indoor use. Also, even if such colored rubber is used outdoors, it must be replaced every January or February.
Or, the current situation is that the color is left as it is and used. The present inventor focused on double bonds or active sites in rubber molecules, and as a result of extensive research on rubber that does not fade or discolor, the inventors discovered a method that is believed to have involved bonding pigment or dye molecules to rubber molecules. As a result, they succeeded in developing a rubber that does not fade or change color, leading to the present invention. The present invention is characterized in that it incorporates one or more electrophilic reagents, a coloring agent selected from the group consisting of organic pigments or dyes having groups that can be modified by the action of said electrophilic reagents, and inorganic pigments. do,
The present invention relates to an unvulcanized rubber composition for forming a colored rubber composition by vulcanization. When the composition of the present invention is heated, at the same time as vulcanization occurs, the polar group present in the organic pigment or dye or the metal atom of the inorganic pigment bonds to the active site present in the rubber molecule, resulting in fading or discoloration. It is believed that a colored rubber composition is formed that does not. As the rubber to be used in the present invention, all rubbers can be used, such as natural rubber (NR) and synthetic rubber. For example, styrene-butadiene rubber (SBR), acrylonitrile-butadiene rubber (NBR), chloroprene rubber (CR), butyl rubber (IIR), polyisoprene rubber (IR), polybutadiene rubber (BR), ethylene-propylene rubber (EPR), and ethylene-propylene. - Synthetic rubbers such as diene terpolymer rubber (EPDM), chlorosulfonated polyethylene (CMS), and ethylene vinyl acetate copolymer (EVA) can be used. The rubber component is required to have double bonds or active sites. The electrophilic reagent plays the role of taking electrons from the terminal polar groups of organic pigments or dyes or the metal atoms of inorganic pigments and charging them. It is a mixture of quinones, tin tetrachloride, aluminum chloride, amphoteric metal oxides such as ZnO and PbO, and weak acid salts of these metals. In particular, tin tetrachloride, a mixture of ZnO and ZnCO 3 , quinones, and AlCl 3 are preferred. This electrophile is added in an amount of 0.2-20 parts per 100 parts of the unvulcanized rubber composition.
parts by weight, preferably 1-12 parts by weight. Many of these electrophilic reagents can be used as long as they do not impair the properties of the vulcanized rubber composition or are decomposed during vulcanization. As the organic pigment or dye, all known organic pigments or dyes having a group that can be modified with an electrophilic reagent can be used. Especially on the benzene nucleus, NH 2 , NO 2 ,
Pigments or dyes in which OCH 3 , OCH 5 , CONH 2 , Cl, CF 3 and the like are present are preferred. Alternatively, almost all inorganic pigments have metal atoms and can therefore be used in the present invention. Examples include zinc white, alumina white, titanium oxide, red iron oxide, litharge, red lead, yellow lead, white lead, zinc yellow, molybdenum red, and cadmium yellow. The amount of pigment or dye used depends on the intended use of the vulcanized rubber composition formed from the rubber composition of the present invention. Other unvulcanized rubber compositions include known sulfur-containing compounds, resin vulcanization accelerators, reinforcing agents, softeners, colorants, extenders, anti-aging agents, and ultraviolet absorbers that are added to ordinary rubber components. Agents etc. may be added. Since the present invention adds an electrophile and a specific pigment or dye to the rubber composition prior to vulcanization, it is believed that the pigment or dye becomes attached to the rubber molecules during the vulcanization process under normal conditions. When using the composition of the present invention, fading or discoloration is less likely to occur than with conventional compositions because the pigment or dye molecules are partially or fully bound to the rubber component. Furthermore, the strength of the vulcanized rubber is further increased by the action of such pigments. Examples of the present invention are shown below. Units are based on weight. Example 1 EPDM 100 parts Stearic acid 1 Process oil 10 Silicic acid 30 Methacrylic acid ester 3 Benzidine Yellow 1 ZnO 5 ZnCO 3 5 Sulfur 2 Diphenylguanidine 2 Unvulcanized rubber composition 175℃, 150℃ for 10 minutes
Vulcanization was carried out at a pressure of Kg/cm 2 . Its properties are shown in Table 1. Comparative Example 1 The procedure of Example 1 was repeated without adding the electrophile ZnCO 3 . The results are shown in Table 1. Comparative example 2 Carbon black instead of benzidine yellow
The procedure of Example 1 was repeated using 41 parts. The results are shown in Table 1. Examples 2-10 The procedure of Example 1 was repeated using the ingredients listed in Table 1. The results are shown in Table 1.

【表】【table】

【表】【table】

【表】【table】

【表】 実施例 11〜14 表2に示された未加硫ゴム組成物を表2に示さ
れたように加硫したその結果を表2に示す。
[Table] Examples 11 to 14 The unvulcanized rubber compositions shown in Table 2 were vulcanized as shown in Table 2. The results are shown in Table 2.

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 硫黄加硫剤、1種又はそれ以上の求電子試
薬、求電子試薬の作用により変性され得る基を有
する有機顔料又は染料および無機顔料からなる群
から選ばれた着色剤を混入したことを特徴とする
硫黄加硫により着色ゴム組成物を形成するための
未加硫ゴム組成物。
1. A coloring agent selected from the group consisting of a sulfur vulcanizing agent, one or more electrophilic reagents, an organic pigment or dye having a group that can be modified by the action of the electrophilic reagent, and an inorganic pigment is mixed therein. An unvulcanized rubber composition for forming a colored rubber composition by sulfur vulcanization.
JP13926383A 1983-07-29 1983-07-29 Unvulcanized rubber composition which forms colored rubber composition by vulcanization Granted JPS6031542A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13926383A JPS6031542A (en) 1983-07-29 1983-07-29 Unvulcanized rubber composition which forms colored rubber composition by vulcanization

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13926383A JPS6031542A (en) 1983-07-29 1983-07-29 Unvulcanized rubber composition which forms colored rubber composition by vulcanization

Publications (2)

Publication Number Publication Date
JPS6031542A JPS6031542A (en) 1985-02-18
JPH0262142B2 true JPH0262142B2 (en) 1990-12-25

Family

ID=15241209

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13926383A Granted JPS6031542A (en) 1983-07-29 1983-07-29 Unvulcanized rubber composition which forms colored rubber composition by vulcanization

Country Status (1)

Country Link
JP (1) JPS6031542A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6047042A (en) * 1983-08-25 1985-03-14 Toa Gomme Kogyo Kk Colored rubber composition
CN108373578A (en) * 2018-04-04 2018-08-07 沈阳体育学院 A kind of preparation method of high resilience Antiskid basketball material for sole of shoe

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5212254A (en) * 1975-07-21 1977-01-29 Dainichi Seika Kogyo Kk Colorants for rubber

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5212254A (en) * 1975-07-21 1977-01-29 Dainichi Seika Kogyo Kk Colorants for rubber

Also Published As

Publication number Publication date
JPS6031542A (en) 1985-02-18

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