JP2022146475A - Tire rubber composition and tire - Google Patents

Tire rubber composition and tire Download PDF

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Publication number
JP2022146475A
JP2022146475A JP2021047455A JP2021047455A JP2022146475A JP 2022146475 A JP2022146475 A JP 2022146475A JP 2021047455 A JP2021047455 A JP 2021047455A JP 2021047455 A JP2021047455 A JP 2021047455A JP 2022146475 A JP2022146475 A JP 2022146475A
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Prior art keywords
carbon black
recycled
mass
tire
rubber composition
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智洋 柏野
Tomohiro Kayano
学 加藤
Manabu Kato
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Yokohama Rubber Co Ltd
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Yokohama Rubber Co Ltd
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Priority to JP2021047455A priority Critical patent/JP2022146475A/en
Priority to PCT/JP2022/012779 priority patent/WO2022202698A1/en
Publication of JP2022146475A publication Critical patent/JP2022146475A/en
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B60VEHICLES IN GENERAL
    • B60CVEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
    • B60C1/00Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B60VEHICLES IN GENERAL
    • B60CVEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
    • B60C15/00Tyre beads, e.g. ply turn-up or overlap
    • B60C15/06Flipper strips, fillers, or chafing strips and reinforcing layers for the construction of the bead
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/04Carbon
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L7/00Compositions of natural rubber
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons

Abstract

To provide a tire rubber composition that solves the problem that the tire strength and heat build-up or the like are greatly reduced when recycled carbon black (recycled CB) is blended into a rubber composition for tire recycling.SOLUTION: The problem is solved by a tire rubber composition that contains diene-based rubber, carbon black (CB) and recycled CB, and in which N2SA of CB is 30 to 90 m2/g and DBP oil absorption is 70 to 140 ml/100 g, N2SA of recycled CB is 65 to 95 m2/g and DBP oil absorption is 75 to 105 ml/100 g, the carbon black total amount in the sum of CB and recycled CB is 30 to 130 pts.mass for 100 pts.mass of diene-based rubber, and the ratio of recycled CB in the total amount of carbon black is 3 to 30 mass%.SELECTED DRAWING: None

Description

本発明は、タイヤ用ゴム組成物およびタイヤに関するものであり、詳しくはカーボンブラック総量の一部を再生カーボンブラックに置換しても、破断強度を維持しつつ、低発熱性を達成し得るタイヤ用ゴム組成物およびそれを用いたタイヤに関するものである。 TECHNICAL FIELD The present invention relates to a rubber composition for a tire and a tire, and more particularly, for a tire capable of maintaining breaking strength and achieving low heat build-up even when part of the total amount of carbon black is replaced with recycled carbon black. The present invention relates to rubber compositions and tires using the same.

近年、資源の保全や環境保護が注目される中、タイヤにおいてもリサイクル率の向上が求められている。そこで廃タイヤなど使用済みのゴム製品を熱分解して得られる再生カーボンブラックの使用が検討されている(例えば下記特許文献1参照)。
しかし再生カーボンブラックにはタイヤの原材料である補強材、タイヤコード等由来の不純物が含まれているため、タイヤの強度や発熱性等が大幅に低下するという問題点がある。
In recent years, as conservation of resources and protection of the environment have attracted attention, improvement in the recycling rate of tires has also been demanded. Therefore, the use of recycled carbon black obtained by pyrolyzing used rubber products such as waste tires has been studied (see, for example, Patent Document 1 below).
However, since recycled carbon black contains impurities derived from reinforcing materials, tire cords, etc., which are raw materials of tires, there is a problem that the strength and heat build-up properties of tires are greatly reduced.

特許6553959号公報Japanese Patent No. 6553959

したがって本発明の目的は、カーボンブラック総量の一部を再生カーボンブラックに置換しても、破断強度を維持しつつ、低発熱性を達成し得るタイヤ用ゴム組成物およびそれを用いたタイヤを提供することにある。 Accordingly, an object of the present invention is to provide a rubber composition for a tire and a tire using the same, which can achieve low heat build-up while maintaining breaking strength even when part of the total amount of carbon black is replaced with recycled carbon black. to do.

本発明者らは鋭意研究を重ねた結果、少なくともジエン系ゴム、カーボンブラックおよび再生カーボンブラックを含むタイヤ用ゴム組成物において、カーボンブラックおよび再生カーボンブラックの窒素吸着比表面積NSAおよびDBP吸油量を特定の範囲に定め、かつ再生カーボンブラックの配合量を適切な範囲に定めることにより、上記課題を解決できることを見出し、本発明を完成することができた。 As a result of extensive studies, the inventors of the present invention have found that in a rubber composition for tires containing at least a diene rubber, carbon black and recycled carbon black, the nitrogen adsorption specific surface area N 2 SA and DBP oil absorption of carbon black and recycled carbon black is set within a specific range and the content of the recycled carbon black is set within an appropriate range.

すなわち本発明は、少なくともジエン系ゴム、カーボンブラックおよび再生カーボンブラックを含むタイヤ用ゴム組成物であって、
前記カーボンブラックの窒素吸着比表面積NSAが30~90m/gであり、かつDBP吸油量が70~140ml/100gであり、
前記再生カーボンブラックの窒素吸着比表面積NSAが65~95m/gであり、かつDBP吸油量が75~105ml/100gであり、
前記カーボンブラックおよび前記再生カーボンブラックの合計のカーボンブラック総量(但し前記再生カーボンブラックに含まれる灰分を除く)が、前記ジエン系ゴム100質量部に対して30~130質量部であり、
前記カーボンブラック総量のうち、前記再生カーボンブラックの割合(但し前記再生カーボンブラックに含まれる灰分を除く)が、3~30質量%である
ことを特徴とするタイヤ用ゴム組成物を提供するものである。
That is, the present invention provides a rubber composition for tires containing at least a diene rubber, carbon black and recycled carbon black,
The carbon black has a nitrogen adsorption specific surface area N 2 SA of 30 to 90 m 2 /g and a DBP oil absorption of 70 to 140 ml/100 g,
The regenerated carbon black has a nitrogen adsorption specific surface area N 2 SA of 65 to 95 m 2 /g and a DBP oil absorption of 75 to 105 ml/100 g,
The total carbon black amount of the carbon black and the recycled carbon black (excluding the ash contained in the recycled carbon black) is 30 to 130 parts by mass with respect to 100 parts by mass of the diene rubber,
A rubber composition for a tire is provided, wherein the ratio of the recycled carbon black (excluding ash contained in the recycled carbon black) in the total amount of carbon black is 3 to 30% by mass. be.

本発明のタイヤ用ゴム組成物は、少なくともジエン系ゴム、カーボンブラックおよび再生カーボンブラックを含むタイヤ用ゴム組成物において、カーボンブラックおよび再生カーボンブラックの窒素吸着比表面積NSAおよびDBP吸油量を特定の範囲に定め、かつ再生カーボンブラックの配合量を適切な範囲に定めているので、カーボンブラック総量の一部を再生カーボンブラックに置換しても、破断強度を維持しつつ、低発熱性を達成し得るタイヤ用ゴム組成物およびそれを用いたタイヤを提供することができる。 The rubber composition for tires of the present invention is a rubber composition for tires containing at least a diene rubber, carbon black and recycled carbon black, wherein the nitrogen adsorption specific surface area N 2 SA and DBP oil absorption of carbon black and recycled carbon black are specified. and the blending amount of recycled carbon black is set within an appropriate range, so even if part of the total amount of carbon black is replaced with recycled carbon black, low heat build-up is achieved while maintaining breaking strength. It is possible to provide a rubber composition for tires that can be used and a tire using the same.

以下、本発明をさらに詳細に説明する。 The present invention will now be described in more detail.

(ジエン系ゴム)
本発明で使用されるジエン系ゴムは、とくに制限されないが、例えば天然ゴム(NR)、イソプレンゴム(IR)、ブタジエンゴム(BR)、スチレン-ブタジエン共重合体ゴム(SBR)、アクリロニトリル-ブタジエン共重合体ゴム(NBR)、エチレン-プロピレン-ジエンターポリマー(EPDM)等が挙げられる。これらは、単独で用いてもよく、2種以上を併用してもよい。また、その分子量やミクロ構造はとくに制限されず、アミン、アミド、シリル、アルコキシシリル、カルボキシル、ヒドロキシル基等で末端変性されていても、エポキシ化されていてもよい。
なお、本発明の前記効果が向上するという観点から、本発明で使用されるジエン系ゴム全体を100質量部としたときに、NRの配合量が30質量部以上、好ましくは30~50質量部であるのがよい。
(Diene rubber)
The diene rubber used in the present invention is not particularly limited, but for example natural rubber (NR), isoprene rubber (IR), butadiene rubber (BR), styrene-butadiene copolymer rubber (SBR), acrylonitrile-butadiene copolymer polymer rubber (NBR), ethylene-propylene-diene terpolymer (EPDM), and the like. These may be used alone or in combination of two or more. Further, its molecular weight and microstructure are not particularly limited, and it may be terminally modified with an amine, amide, silyl, alkoxysilyl, carboxyl, hydroxyl group or the like, or epoxidized.
From the viewpoint of improving the effects of the present invention, the amount of NR compounded is 30 parts by mass or more, preferably 30 to 50 parts by mass, when the entire diene rubber used in the present invention is 100 parts by mass. should be

(カーボンブラック)
本発明で使用するカーボンブラック(CB)は、窒素吸着比表面積NSAが30~90m/gであり、かつDBP吸油量が70~140ml/100gである。
CBのNSAが30m/g未満であると破断強度が低下し、90m/gを超えると低発熱性が得られない。
CBのDBP吸油量が70ml/100g未満であると破断強度が低下し、140ml/100gを超えると低発熱性が悪化する。
本発明において、CBのNSAは30~70m/gが好ましく、DBP吸油量は80~120ml/100gが好ましい。
(Carbon black)
The carbon black (CB) used in the present invention has a nitrogen adsorption specific surface area N 2 SA of 30-90 m 2 /g and a DBP oil absorption of 70-140 ml/100 g.
When the N 2 SA of the CB is less than 30 m 2 /g, the breaking strength is lowered, and when it exceeds 90 m 2 /g, low heat build-up cannot be obtained.
When the DBP oil absorption of CB is less than 70 ml/100 g, the breaking strength is lowered, and when it exceeds 140 ml/100 g, the low heat build-up deteriorates.
In the present invention, the N 2 SA of CB is preferably 30-70 m 2 /g, and the DBP oil absorption is preferably 80-120 ml/100 g.

(再生カーボンブラック)
本発明で使用する再生カーボンブラック(再生CB)は、例えば廃タイヤの熱分解を経て生成される再生CBであることができる。廃タイヤの熱分解は公知の方法にしたがって行うことができる。例えば、650℃以上の温度の熱分解法が挙げられる。
本発明で使用する再生CBは、窒素吸着比表面積NSAが65~95m/gであり、かつDBP吸油量が75~105ml/100gである。再生CBのNSAおよびDBP吸油が前記範囲を外れると、本発明の効果を奏することができない。
なお、本発明における再生CBは市販されているものを利用することができ、例えばEnrestec社製商品名PB365が挙げられる。PB365は、廃タイヤの熱分解を経て生成される再生CBであり、NSAが76m/gであり、DBP吸油量が88ml/100gである。また、PB365は灰分を17質量%程度含んでいる。前記灰分に含まれる代表的な元素組成は、以下の通りである。
(recycled carbon black)
Recycled carbon black (recycled CB) used in the present invention can be, for example, recycled CB produced through thermal decomposition of waste tires. Pyrolysis of waste tires can be carried out according to known methods. For example, a pyrolysis method at a temperature of 650° C. or higher can be mentioned.
The regenerated CB used in the present invention has a nitrogen adsorption specific surface area N 2 SA of 65-95 m 2 /g and a DBP oil absorption of 75-105 ml/100 g. If the N 2 SA and DBP oil absorption of the recycled CB are outside the above ranges, the effect of the present invention cannot be obtained.
As the regenerated CB in the present invention, a commercially available one can be used, for example PB365 (trade name) manufactured by Enrestec. PB365 is recycled CB produced through thermal decomposition of waste tires, and has an N 2 SA of 76 m 2 /g and a DBP oil absorption of 88 ml/100 g. Moreover, PB365 contains about 17% by mass of ash. A typical elemental composition contained in the ash is as follows.

Figure 2022146475000001
Figure 2022146475000001

なお本発明において、NSAは、JIS K6217-2に準拠し、DBP吸油量はASTM D2414に準拠し、灰分は、公知のICP法により測定される。 In the present invention, N 2 SA conforms to JIS K6217-2, DBP oil absorption conforms to ASTM D2414, and ash content is measured by a known ICP method.

(ゴム組成物の配合割合)
本発明のゴム組成物は、少なくとも前記ジエン系ゴム、前記CBおよび前記再生CBを含み、前記CBおよび前記再生CBの合計のカーボンブラック総量(但し前記再生CBに含まれる灰分を除く)が、前記ジエン系ゴム100質量部に対して30~130質量部(好ましくは60~100質量部)であり、前記カーボンブラック総量のうち、前記再生CBの割合(但し前記再生CBに含まれる灰分を除く)が、3~30質量%(好ましくは5~15質量%)であることを特徴とする。
前記カーボンブラック総量が、前記ジエン系ゴム100質量部に対し30質量部未満であると、破断強度が低下し、逆に130質量部を超えると低発熱性が悪化する。
前記カーボンブラック総量のうち、前記再生CBの割合が3質量%未満であると、低発熱性が悪化し、逆に30質量%を超えると破断強度が悪化する。
(Mixing ratio of rubber composition)
The rubber composition of the present invention contains at least the diene rubber, the CB and the recycled CB, and the total carbon black amount of the CB and the recycled CB (excluding ash contained in the recycled CB) is 30 to 130 parts by mass (preferably 60 to 100 parts by mass) with respect to 100 parts by mass of diene rubber, and the ratio of the recycled CB to the total amount of carbon black (excluding ash contained in the recycled CB) is 3 to 30% by mass (preferably 5 to 15% by mass).
When the total amount of carbon black is less than 30 parts by mass with respect to 100 parts by mass of the diene rubber, the breaking strength is lowered, and when it exceeds 130 parts by mass, the low heat build-up deteriorates.
When the proportion of the recycled CB in the total amount of carbon black is less than 3% by mass, low heat build-up deteriorates, and when it exceeds 30% by weight, the strength at break deteriorates.

(その他成分)
本発明におけるゴム組成物には、前記した成分に加えて、加硫又は架橋剤;加硫又は架橋促進剤;シリカ、クレー、タルク、炭酸カルシウムのような各種充填剤;老化防止剤;可塑剤;樹脂;硬化剤などのゴム組成物に一般的に配合されている各種添加剤を配合することができ、かかる添加剤は一般的な方法で混練して組成物とし、加硫又は架橋するのに使用することができる。これらの添加剤の配合量も、本発明の目的に反しない限り、従来の一般的な配合量とすることができる。
(Other ingredients)
In addition to the above components, the rubber composition of the present invention includes vulcanizing or cross-linking agents; vulcanizing or cross-linking accelerators; various fillers such as silica, clay, talc and calcium carbonate; anti-aging agents; ; Resin; Various additives generally blended in rubber compositions such as curing agents can be blended. can be used for The blending amount of these additives can also be a conventional general blending amount as long as it does not contradict the object of the present invention.

本発明のゴム組成物は、カーボンブラック総量の一部を再生カーボンブラックに置換しても、破断強度を維持しつつ、低発熱性を達成し得ることから、タイヤのケーシング部材(アンダートレッド、サイドトレッド、リムクッション等)に好適に用いられ得る。また本発明のタイヤは、空気入りタイヤであることが好ましく、空気、窒素等の不活性ガス及びその他の気体を充填することができる。 The rubber composition of the present invention can achieve low heat build-up while maintaining breaking strength even when part of the total amount of carbon black is replaced with recycled carbon black. tread, rim cushion, etc.). Moreover, the tire of the present invention is preferably a pneumatic tire, and can be filled with air, an inert gas such as nitrogen, or other gases.

以下、本発明を実施例および比較例によりさらに説明するが、本発明は下記例に制限されるものではない。 The present invention will be further described below with reference to examples and comparative examples, but the present invention is not limited to the following examples.

標準例1~2、実施例1~6および比較例1~8
サンプルの調製
表2に示す配合(質量部)において、加硫系(加硫促進剤、硫黄)を除く成分を1.7リットルの密閉式バンバリーミキサーで5分間混練した後、ミキサー外に放出させて室温冷却した。続いて、該組成物を同バンバリーミキサーに再度入れ、加硫系を加えて混練し、ゴム組成物を得た。次に得られたゴム組成物を所定の金型中で150℃で30分間プレス加硫して加硫ゴム試験片を調製した。得られた加硫ゴム試験片について以下に示す試験法で物性を測定した。
Standard Examples 1-2, Examples 1-6 and Comparative Examples 1-8
Sample preparation In the formulation (parts by mass) shown in Table 2, the components except for the vulcanization system (vulcanization accelerator, sulfur) were kneaded in a 1.7-liter closed Banbury mixer for 5 minutes, and then discharged out of the mixer. and cooled to room temperature. Subsequently, the composition was placed in the same Banbury mixer again, and the vulcanizing system was added and kneaded to obtain a rubber composition. Next, the obtained rubber composition was press-vulcanized in a predetermined mold at 150° C. for 30 minutes to prepare a vulcanized rubber test piece. The physical properties of the obtained vulcanized rubber test pieces were measured by the following test methods.

破断強度(TB):JIS K 6251に従い、室温で試験した。結果は標準例1または2の値を100として指数表示した。指数が大きいほど、破断強度に優れることを示す。
tanδ(60℃):JIS K6394:2007に準じて、粘弾性スペクトロメーター(東洋精機製作所製)を用い、伸張変形歪率10±2%、振動数20Hz、温度60℃の条件で、tanδ(60℃)を測定した。結果は、標準例1または2の値を100として指数表示した。指数が小さいほど、低発熱性であることを示す。
なお、比較例1~4および実施例1~3は標準例1と比較され、比較例5~8および実施例4~6は標準例2と比較される。
Breaking strength (TB): Tested at room temperature according to JIS K 6251. The results were indexed with the value of Standard Example 1 or 2 as 100. A larger index indicates better breaking strength.
tan δ (60 ° C.): According to JIS K6394: 2007, using a viscoelastic spectrometer (manufactured by Toyo Seiki Seisakusho), under conditions of extension deformation strain rate 10 ± 2%, frequency 20 Hz, temperature 60 ° C., tan δ (60 °C) was measured. The results were indexed with the value of Standard Example 1 or 2 as 100. A smaller index indicates a lower heat build-up.
Comparative Examples 1-4 and Examples 1-3 are compared with Standard Example 1, and Comparative Examples 5-8 and Examples 4-6 are compared with Standard Example 2.

結果を表2に示す。 Table 2 shows the results.

Figure 2022146475000002
Figure 2022146475000002

*1:NR(PT.KIRANA SAPTA製SIR20)
*2:SBR(ZSエラストマー株式会社製 Nipol 1502)
*3:BR(ZSエラストマー株式会社製 Nipol BR1220)
*4:GPFカーボンブラック1(日鉄カーボン株式会社製ニテロン#GN、窒素吸着比表面積(NSA)=32m/g、DBP吸油量=82ml/100g)
*5:FEFカーボンブラック2(日鉄カーボン株式会社製ニテロン#10N、窒素吸着比表面積(NSA)=40m/g、DBP吸油量=120ml/100g)
*6:SAFカーボンブラック3(東海カーボン株式会社製シースト9M、窒素吸着比表面積(NSA)=150m/g、DBP吸油量=113ml/100g)
*7:SRFカーボンブラック4(東海カーボン株式会社製シーストG-FY、窒素吸着比表面積(NSA)=27m/g、DBP吸油量=65ml/100g)
*8:再生カーボンブラック(Enrestec社製商品名PB365、窒素吸着比表面積(NSA)=76m/g、DBP吸油量=88ml/100g)
*9:酸化亜鉛(正同化学工業株式会社製酸化亜鉛3種)
*10:ステアリン酸(日油株式会社製ビーズステアリン酸YR)
*11:老化防止剤(EASTMAN社製6PPD)
*12:オイル(昭和シェル石油株式会社製エキストラクト4号S)
*13:硫黄(四国化成工業株式会社製ミュークロンOT-20)
*14:加硫促進剤TBBS(三新化学工業株式会社製サンセラーNS-G)
*1: NR (SIR20 made by PT.KIRANA SAPTA)
*2: SBR (Nipol 1502 manufactured by ZS Elastomer Co., Ltd.)
*3: BR (Nipol BR1220 manufactured by ZS Elastomer Co., Ltd.)
*4: GPF carbon black 1 (Niteron #GN manufactured by Nippon Steel Carbon Co., Ltd., nitrogen adsorption specific surface area (N 2 SA) = 32 m 2 /g, DBP oil absorption = 82 ml/100 g)
*5: FEF carbon black 2 (Niteron #10N manufactured by Nippon Steel Carbon Co., Ltd., nitrogen adsorption specific surface area (N 2 SA) = 40 m 2 /g, DBP oil absorption = 120 ml/100 g)
*6: SAF carbon black 3 (SEAST 9M manufactured by Tokai Carbon Co., Ltd., nitrogen adsorption specific surface area (N 2 SA) = 150 m 2 /g, DBP oil absorption = 113 ml/100 g)
*7: SRF carbon black 4 (SEAST G-FY manufactured by Tokai Carbon Co., Ltd., nitrogen adsorption specific surface area (N 2 SA) = 27 m 2 /g, DBP oil absorption = 65 ml/100 g)
*8: Recycled carbon black (manufactured by Enrestec, trade name PB365, nitrogen adsorption specific surface area (N 2 SA) = 76 m 2 /g, DBP oil absorption = 88 ml/100 g)
*9: Zinc oxide (Type 3 zinc oxide manufactured by Seido Chemical Industry Co., Ltd.)
* 10: Stearic acid (bead stearic acid YR manufactured by NOF Corporation)
* 11: Anti-aging agent (6PPD manufactured by EASTMAN)
*12: Oil (Extract No. 4S manufactured by Showa Shell Sekiyu K.K.)
*13: Sulfur (Mucron OT-20 manufactured by Shikoku Kasei Co., Ltd.)
*14: Vulcanization accelerator TBBS (Suncellar NS-G manufactured by Sanshin Chemical Industry Co., Ltd.)

表2の結果から、実施例1~6のゴム組成物は、少なくともジエン系ゴム、カーボンブラックおよび再生カーボンブラックを含むタイヤ用ゴム組成物において、カーボンブラックおよび再生カーボンブラックの窒素吸着比表面積NSAおよびDBP吸油量を特定の範囲に定め、かつ再生カーボンブラックの配合量を適切な範囲に定めているので、標準例1または2のゴム組成物に比べ、カーボンブラック総量の一部を再生カーボンブラックに置換しても、破断強度を維持しつつ、低発熱性を達成し得ることが分かる。
一方、比較例1、5は、カーボンブラック総量のうち、再生カーボンブラックの割合(但し前記再生カーボンブラックに含まれる灰分を除く)が約37.2質量%であるので(PB365の配合量25質量部のうち、灰分が17質量%であるので、カーボンブラック総量は、CB35質量部+(再生CB25質量部-再生CB灰分4.25質量部)=55.75質量部であり、再生CBの割合は、20.75質量部/55.75質量部 × 100=37.2質量%となる)、破断強度が悪化した。
比較例2、6は、配合したカーボンブラックの全てが再生カーボンブラックであるので、破断強度が悪化した。
比較例3、7は、配合したカーボンブラックの窒素吸着比表面積NSAが本発明で規定する上限を超えているので、発熱性が悪化した。
比較例4、8は、配合したカーボンブラックの窒素吸着比表面積NSAが本発明で規定する下限未満であるので、破断強度が悪化した。
From the results in Table 2, the rubber compositions of Examples 1 to 6 are tire rubber compositions containing at least a diene rubber, carbon black and recycled carbon black, and the nitrogen adsorption specific surface area of carbon black and recycled carbon black is N 2 Since the SA and DBP oil absorptions are set within specific ranges, and the blending amount of recycled carbon black is set within an appropriate range, compared to the rubber composition of Standard Example 1 or 2, part of the total amount of carbon black is recycled carbon It can be seen that even when replaced with black, low heat build-up can be achieved while maintaining breaking strength.
On the other hand, in Comparative Examples 1 and 5, the proportion of recycled carbon black in the total amount of carbon black (excluding the ash contained in the recycled carbon black) was about 37.2% by mass (the amount of PB365 blended was 25 mass Of the parts, the ash content is 17% by mass, so the total amount of carbon black is 35 parts by mass of CB + (25 parts by mass of recycled CB - 4.25 parts by mass of recycled CB ash) = 55.75 parts by mass, and the ratio of recycled CB is 20.75 mass parts/55.75 mass parts x 100 = 37.2 mass%), and the breaking strength deteriorated.
In Comparative Examples 2 and 6, all of the carbon black blended was recycled carbon black, so the breaking strength was deteriorated.
In Comparative Examples 3 and 7, the nitrogen adsorption specific surface area N 2 SA of the blended carbon black exceeded the upper limit specified in the present invention, so the heat build-up deteriorated.
Comparative Examples 4 and 8 deteriorated in breaking strength because the nitrogen adsorption specific surface area N 2 SA of the blended carbon black was less than the lower limit specified in the present invention.

Claims (3)

少なくともジエン系ゴム、カーボンブラックおよび再生カーボンブラックを含むタイヤ用ゴム組成物であって、
前記カーボンブラックの窒素吸着比表面積NSAが30~90m/gであり、かつDBP吸油量が70~140ml/100gであり、
前記再生カーボンブラックの窒素吸着比表面積NSAが65~95m/gであり、かつDBP吸油量が75~105ml/100gであり、
前記カーボンブラックおよび前記再生カーボンブラックの合計のカーボンブラック総量(但し前記再生カーボンブラックに含まれる灰分を除く)が、前記ジエン系ゴム100質量部に対して30~130質量部であり、
前記カーボンブラック総量のうち、前記再生カーボンブラックの割合(但し前記再生カーボンブラックに含まれる灰分を除く)が、3~30質量%である
ことを特徴とするタイヤ用ゴム組成物。
A tire rubber composition comprising at least a diene rubber, carbon black and recycled carbon black,
The carbon black has a nitrogen adsorption specific surface area N 2 SA of 30 to 90 m 2 /g and a DBP oil absorption of 70 to 140 ml/100 g,
The regenerated carbon black has a nitrogen adsorption specific surface area N 2 SA of 65 to 95 m 2 /g and a DBP oil absorption of 75 to 105 ml/100 g,
The total carbon black amount of the carbon black and the recycled carbon black (excluding the ash contained in the recycled carbon black) is 30 to 130 parts by mass with respect to 100 parts by mass of the diene rubber,
A rubber composition for a tire, wherein the ratio of the recycled carbon black (excluding ash contained in the recycled carbon black) to the total amount of the carbon black is 3 to 30% by mass.
前記ジエン系ゴム100質量部中、天然ゴムの割合が30質量部以上であることを特徴とする請求項1に記載のタイヤ用ゴム組成物。 2. The rubber composition for a tire according to claim 1, wherein the proportion of natural rubber in 100 parts by mass of said diene rubber is 30 parts by mass or more. 請求項1または2に記載のタイヤ用ゴム組成物を用いたタイヤ。 A tire using the rubber composition for tires according to claim 1 or 2.
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Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55500113A (en) * 1978-02-15 1980-02-28
JP2011046299A (en) * 2009-08-27 2011-03-10 Yokohama Rubber Co Ltd:The Pneumatic tire
JP2012001682A (en) * 2010-06-21 2012-01-05 Bridgestone Corp Rubber composition and tire using the same
CN102634075A (en) * 2012-04-25 2012-08-15 杭州电子科技大学 Rubber reinforcing method
JP2012521443A (en) * 2009-03-24 2012-09-13 リッペ リソース リカバリー コーポレイション Method for recycling carbonaceous material from waste tire and product derived from waste tire
JP2013151584A (en) * 2012-01-24 2013-08-08 Toyo Tire & Rubber Co Ltd Rubber composition for rubber vibration isolator
JP2014031425A (en) * 2012-08-02 2014-02-20 Yokohama Rubber Co Ltd:The Rubber composition for tire rim cushion or gum finishing and pneumatic tire using the same
CN104479722A (en) * 2014-05-12 2015-04-01 中机国宏(北京)高分子裂解技术研究院 Continuous segmented cracking equipment and technology used for waste and old tyres and capable of preventing generation of dioxin
EP3173251A1 (en) * 2015-11-27 2017-05-31 Bridgestone Corporation Rubber compound for tyres comprising recycled carbon black
JP2020523456A (en) * 2017-06-29 2020-08-06 株式会社ブリヂストン Rubber compound for pneumatic tires containing recycled carbon black

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111455183B (en) * 2020-05-14 2022-03-01 沈阳鑫迪环境技术有限公司 Method for purifying and recovering lead and zinc by waste tire cracking carbon black

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55500113A (en) * 1978-02-15 1980-02-28
JP2012521443A (en) * 2009-03-24 2012-09-13 リッペ リソース リカバリー コーポレイション Method for recycling carbonaceous material from waste tire and product derived from waste tire
JP2011046299A (en) * 2009-08-27 2011-03-10 Yokohama Rubber Co Ltd:The Pneumatic tire
JP2012001682A (en) * 2010-06-21 2012-01-05 Bridgestone Corp Rubber composition and tire using the same
JP2013151584A (en) * 2012-01-24 2013-08-08 Toyo Tire & Rubber Co Ltd Rubber composition for rubber vibration isolator
CN102634075A (en) * 2012-04-25 2012-08-15 杭州电子科技大学 Rubber reinforcing method
JP2014031425A (en) * 2012-08-02 2014-02-20 Yokohama Rubber Co Ltd:The Rubber composition for tire rim cushion or gum finishing and pneumatic tire using the same
CN104479722A (en) * 2014-05-12 2015-04-01 中机国宏(北京)高分子裂解技术研究院 Continuous segmented cracking equipment and technology used for waste and old tyres and capable of preventing generation of dioxin
EP3173251A1 (en) * 2015-11-27 2017-05-31 Bridgestone Corporation Rubber compound for tyres comprising recycled carbon black
JP2020523456A (en) * 2017-06-29 2020-08-06 株式会社ブリヂストン Rubber compound for pneumatic tires containing recycled carbon black

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