JP5438169B2 - Rubber composition and tire using the same - Google Patents

Description

  The present invention relates to a rubber composition and a tire using the rubber composition.

  In recent years, while the performance of automobiles has increased and the horsepower has increased, awareness of safety has increased, and the demand for grip performance on tires has increased. For example, various performances during high-speed traveling are listed as one of them. In particular, the tire tread has a problem that heat is generated as the vehicle travels, and grip performance deteriorates due to high temperatures.

  Conventionally, as a technique for improving grip performance, for example, a technique of increasing the glass transition point (Tg) by increasing the amount of bound styrene and the amount of vinyl bond of styrene-butadiene rubber is known. However, there is a risk that the wear resistance is lowered, or the grip performance at a low temperature is lowered and brittle fracture is caused. As a technique for improving grip performance, a technique of blending a large amount of oil is also known. In this case, however, the wear resistance is lowered. In addition, a method of blending a resin having a high Tg with a rubber composition for a tire tread is also known. However, the grip performance under high temperature conditions could not be sufficiently improved.

  In order to solve these problems, for example, a method of blending a piperidine compound with a protonic acid or a phenol derivative (see Patent Document 1) is known. However, the rubber strength is not sufficient, and there is still room for improvement in grip performance under high temperature conditions.

JP-A-2005-112922

  An object of this invention is to provide the rubber composition which can improve abrasion resistance and the grip performance in a wide temperature range, and a tire using the same.

  The present invention comprises (A) a rubber component, (B) a nitrogen compound, (C) an organometallic compound, and (D) a phenolic compound, an aromatic carboxylic acid, and an aliphatic carboxylic acid having 15 or less carbon atoms. The present invention relates to a rubber composition containing at least one selected proton acid.

The nitrogen compound (B) has the chemical formula (1):

(In the formula, R ¹ is a monovalent chain hydrocarbon group, —OH, —NH ₂ or —SH, a is an integer of 0 to 4, and a R ¹ may be the same or different. Well, the total carbon number of R ¹ is 10 or less)
It is preferable that it is imidazole (I) represented by these.

The nitrogen compound (B)
Chemical formula (2):

(Wherein R ² and R ³ are monovalent chain hydrocarbon groups, —OH, —NH ₂ or —SH, R ⁴ is a divalent chain hydrocarbon group, and X is a nitrogen atom. a cyclic structure including d, X may include a double bond, b is an integer of 0 to 3, c is an integer of 0 to 5, d is an integer of 1 to 6, and b R ² and c R ^{3 s} may be the same or different, and d N may be adjacent or non-adjacent), or chemical formula (3):

(In the formula, R ⁵ is a monovalent chain hydrocarbon group, —OH, —NH ₂ or —SH, e is an integer of 0 to 4, and e R ⁵ may be the same or different. Well, the total carbon number of R ⁵ is 11-15)
It is preferable that they are imidazoles (II) represented by these, or the mixture of imidazoles (I) and imidazoles (II).

Protic acid (D) is R ⁶ —COOH (R ⁶ is a monovalent chain hydrocarbon group having 1 to 10 carbon atoms), or chemical formula (4):

(Wherein R ⁷ is a monovalent chain hydrocarbon group, —OH, —NH ₂ or —SH, f is an integer of 0 to 5, and f R ^{7 s} may be the same or different. Well, the total carbon number of R ⁷ is 10 or less)
Or a chemical formula (5):

Wherein R ⁸ is a monovalent chain hydrocarbon group, —OH, —NH ₂ or —SH, g is an integer of 0 to 5, and g R ⁸ may be the same or different. Well, the total carbon number of R ⁸ is 10 or less)
It is preferable that it is a phenol type compound represented by these.

  The present invention also relates to a tire using the rubber composition.

  According to the present invention, by containing a rubber component, a nitrogen compound, an organometallic compound, and a proton acid, a rubber composition that can improve wear resistance and grip performance in a wide temperature range, and a tire using the rubber composition Can be provided.

  The rubber composition of the present invention contains a rubber component (A), a nitrogen compound (B), an organometallic compound (C) and a protonic acid (D).

  Examples of the rubber component (A) include natural rubber (NR), isoprene rubber (IR), styrene butadiene rubber (SBR), butadiene rubber (BR), butyl rubber (IIR), halogenated butyl rubber (X-IIR), and acrylonitrile. Examples include butadiene rubber (NBR), ethylene propylene diene rubber (EPDM), chloroprene rubber (CR), and halides of copolymers of isomonoolefin and paraalkylstyrene, which are usually used in the rubber industry. There is no restriction | limiting in particular, You may use individually or in combination of 2 or more types. Among them, NR, SBR or BR is preferable, and SBR is more preferable because it has sufficient strength and exhibits excellent wear resistance.

  The amount of bound styrene of SBR is preferably 10% by weight or more, more preferably 20% by weight or more, further preferably 30% by weight or more, and particularly preferably 35% by weight or more. When the amount of bound styrene of SBR is less than 10% by weight, there is a tendency that a sufficient improvement effect of grip performance cannot be obtained under medium temperature and high temperature conditions. The amount of bound styrene in SBR is preferably 60% by weight or less, more preferably 50% by weight or less, and further preferably 45% by weight or less. When the amount of bound styrene in SBR exceeds 60% by weight, the rubber becomes hard, the contact area with the road surface decreases, and high grip performance tends to be not obtained.

  The nitrogen compound (B) preferably contains hydrogen bonds, and by adding such a nitrogen compound to the rubber composition, the grip performance under intermediate temperature conditions (30 to 50 ° C.) is improved. be able to.

  The nitrogen compound (B) preferably has one or more cyclic structures containing nitrogen. If no annular structure containing nitrogen is included, the high temperature grip performance tends not to be improved.

  Examples of such a nitrogen compound (B) include piperidine derivatives, imidazoles, caprolactams and the like. Among these, imidazoles are preferable because they are general-purpose products and easily available.

When imidazoles are used as the nitrogen compound (B), the nitrogen compound (B) has the chemical formula (1):

(In the formula, R ¹ is a monovalent chain hydrocarbon group, —OH, —NH ₂ or —SH, a is an integer of 0 to 4, and a R ¹ may be the same or different. The total number of carbon atoms of R ¹ is preferably 10 or less), but the imidazoles (I) represented by formula (2):

(Wherein R ² and R ³ are monovalent chain hydrocarbon groups, —OH, —NH ₂ or —SH, R ⁴ is a divalent chain hydrocarbon group, and X is a nitrogen atom. a cyclic structure including d, X may include a double bond, b is an integer of 0 to 3, c is an integer of 0 to 5, d is an integer of 1 to 6, and b R ² and c R ^{3 s} may be the same or different, and d N may be adjacent or non-adjacent), or chemical formula (3):

(In the formula, R ⁵ is a monovalent chain hydrocarbon group, —OH, —NH ₂ or —SH, e is an integer of 0 to 4, and e R ⁵ may be the same or different. Well, the total carbon number of R ⁵ is 11 to 15), or a mixture of imidazoles (I) and imidazoles (II) may be used.

In the chemical formula (1), R ¹ is preferably a monovalent chain hydrocarbon group, —OH, —NH ₂ and —SH. Among them, a monovalent chain hydrocarbon group is more preferable, an alkyl group is more preferable, and —CH ₃ is particularly preferable because there is little steric hindrance and the reaction with the protonic acid (D) easily occurs effectively. preferable.

The number a of the substituents R ¹ is preferably an integer of 0 to 4, for the reason that can be a number of substituents R ¹ is large, the steric hindrance, 0 or 1 are more preferable.

Further, the total carbon number of R ¹ is preferably 10 or less, and more preferably 5 or less. When the total carbon number of R ¹ is 11 or more, the steric hindrance is large, hydrogen bonds cannot be formed effectively, and a sufficient improvement effect of grip performance tends not to be obtained.

などがあげられる。なかでも、 As imidazoles satisfying the chemical formula (1), for example,

Etc. Above all,

が好ましい。

Is preferred.

In the chemical formula (2), R ² and R ³ are preferably a monovalent chain hydrocarbon group, —OH, —NH ₂ and —SH. Among these, as R ² , a monovalent chain hydrocarbon group is preferable, an alkyl group is more preferable, because there is little steric hindrance and reaction with a protonic acid (D) is likely to occur effectively. CH ₃ or —C ₂ H ₅ is more preferred. R ³ is preferably —NH ₂ . Note that b R ² and c R ³ may be the same or different. In addition, the number b of the substituent R ² is preferably an integer of 0 to 3, and the number of substituents should not be too large, but a substituent having a small number of carbon atoms is used rather than adding one substituent having a large number of carbon atoms. It is more preferable to use 2 for the reason that the number of steric hindrances is smaller.

The number c of the substituent R ³ is preferably an integer of 0 to 5, and more preferably 2.

  X is a cyclic structure containing d nitrogen atoms, and X may contain a double bond.

  The number d of N in X is preferably an integer of 1 to 6, and more preferably 3. Note that d Ns may or may not be adjacent.

などがあげられる。なかでも、 As such a cyclic structure X, for example,

Etc. Above all,

が好ましい。

Is preferred.

R ⁴ is preferably a divalent chain hydrocarbon group, more preferably an alkylene group, and further preferably —C ₂ H ₄ —.

などがあげられる。なかでも、汎用品で入手しやすいという理由から、 As imidazoles satisfying the chemical formula (2), for example,

Etc. Above all, because it is easy to obtain with general-purpose products,

が好ましい。

Is preferred.

In chemical formula (3), R ⁵ is preferably a monovalent chain hydrocarbon group, —OH, —NH ₂ and —SH.

The number e of the substituent R ⁵ is an integer of 0 to 4, and 0 or 1 is preferable because the steric hindrance is small.

The total carbon number of R ⁵ is preferably an integer of 11 to 15. When the total carbon number of R ⁵ is 16 or more, there is a tendency that it does not easily react with the protonic acid due to steric hindrance.

などがあげられる。 As imidazoles satisfying the chemical formula (3), for example,

Etc.

  The nitrogen compound (B) may be used alone or in combination of two or more. However, combining two or more of the nitrogen compounds (B) is less effective and further reduces the rubber strength. Is preferably used. However, the combination of imidazole (I) and imidazole (II) is preferable because the low-temperature characteristics can be improved while maintaining high-temperature grip performance.

  The compounding amount of the nitrogen compound (B) is preferably 0.1 parts by weight or more and more preferably 2 parts by weight or more with respect to 100 parts by weight of the rubber component (A). When the compounding amount of the nitrogen compound (B) is less than 0.1 part by weight, the grip performance improving effect due to the nitrogen compound (B) tends to be difficult to obtain. Further, the compounding amount of the nitrogen compound (B) is preferably 30 parts by weight or less, and more preferably 20 parts by weight or less. When the compounding amount of the nitrogen compound (B) exceeds 30 parts by weight, the effect of adding the compound (B) becomes difficult to obtain, and the cost tends to increase.

  The organometallic compound (C) preferably contains an ionic bond. By blending such an organometallic compound in the rubber composition, the grip performance under high temperature conditions (around 100 ° C.) is improved. be able to.

  Examples of the organic metal compound (C) include organic carboxylic acid metal salts and thiocarboxylic acid salts, but organic carboxylic acid metal salts are preferred because they are easily available.

  Examples of organic carboxylic acid metal salts include aromatic carboxylic acid metal salts such as benzoic acid metal salts and naphthoic acid metal salts, acetic acid metal salts, propionic acid metal salts, acrylic acid metal salts, methacrylic acid metal salts, and oxalic acid metal salts. The carboxylic acid metal salt which does not contain an aromatic ring is mentioned, and the carboxylic acid metal salt which does not contain an aromatic ring is preferred.

  Carboxylic acid metal salts that do not contain aromatic rings include carboxylic acid metal salts that do not contain multiple bonds such as metal acetates, metal propionates, metal oxalates, metal bonds such as metal acrylates and metal methacrylates. The carboxylic acid metal salt containing a carboxylic acid metal salt containing no multiple bond is more preferable because it can suppress variation in crosslinking and improve the crosslinking density.

  Examples of carboxylic acid metal salts that do not contain multiple bonds include organic monocarboxylic acid metal salts such as acetic acid metal salts and propionic acid metal salts, and organic dicarboxylic acid metal salts such as oxalic acid metal salts. More preferred are monocarboxylic acid metal salts.

  Examples of the organic carboxylic acid metal salt satisfying the above conditions include magnesium acetate, calcium propionate, calcium acetate, magnesium propionate and the like, but since they are generally commercially available and easy to obtain, magnesium acetate or calcium propionate is used. preferable.

  Examples of the thiocarboxylate include thioacetate and thiopropionate.

  The organometallic compound (C) may be used alone or in combination of two or more, but when two or more are used in combination, two or more compounds having an ionic bond may be used in combination. It is difficult to obtain the effect of the combination, and the rubber strength is lowered, which is not preferable.

  The content of the organometallic salt compound (C) is preferably 0.1 parts by weight or more and more preferably 1 part by weight or more with respect to 100 parts by weight of the rubber component (A). When the content of the organometallic salt compound (C) is less than 0.1 parts by weight, the grip performance improving effect due to the inclusion of the organometallic compound (C) tends to be difficult to obtain. Moreover, 30 weight part or less is preferable and, as for content of an organometallic compound (C), 20 weight part or less is more preferable. When the content of the organometallic compound (C) exceeds 30 parts by weight, the tackiness tends to increase.

  Examples of the protonic acid (D) include carboxylic acids and phenolic compounds, and phenolic compounds are preferred because they have little crosslinking inhibition.

As the carboxylic acid, R ⁶ —COOH (R ⁶ is a monovalent chain hydrocarbon group having 1 to 10 carbon atoms) or chemical formula (4):

(Wherein R ⁷ is a monovalent chain hydrocarbon group, —OH, —NH ₂ or —SH, f is an integer of 0 to 5, and f R ^{7 s} may be the same or different. The total carbon number of R ⁷ is preferably 10 or less).

R ⁶ is preferably a monovalent chain hydrocarbon group having 10 or less carbon atoms, and a methyl group is more preferable because it is easily available.

Acetic acid, propionic acid, etc. can be used as the carboxylic acid represented by R ⁶ —COOH.

In the chemical formula (4), R ⁷ is preferably a monovalent chain hydrocarbon group, —OH, —NH ₂ and —SH.

The number f of the substituent R ⁷ is an integer of 0 to 4, and 0 is preferable because it is easily available.

Further, the total carbon number of R ⁷ is preferably 10 or less, and more preferably 5 or less. When the total carbon number of R ⁷ is 11 or more, the steric hindrance is large, and it tends to be difficult to react with the protonic acid.

などがあげられる。 As the carboxylic acid satisfying the chemical formula (4), for example,

Etc.

As a phenolic compound, chemical formula (5):

Wherein R ⁸ is a monovalent chain hydrocarbon group, —OH, —NH ₂ or —SH, g is an integer of 0 to 5, and g R ⁸ may be the same or different. The total number of carbon atoms of R ⁸ is preferably 10 or less).

In the chemical formula (5), R ⁸ is preferably a monovalent chain hydrocarbon group, —OH, —NH ₂ and —SH. Among these, a monovalent chain hydrocarbon group, —OH is more preferable, an alkyl group or —OH is more preferable, and —C ₂ H ₅ , —C (CH ₃ ), — OH is particularly preferred.

The number g of the substituent R ⁸ is preferably an integer of 0 to 5, and more preferably 0 to 3 because the steric hindrance is small.

Further, the total carbon number of R ⁸ is preferably 10 or less. When the total carbon number of R ⁸ is 11 or more, the steric hindrance is large, and it tends to be difficult to react with the protonic acid.

などがあげられる。 Examples of the phenolic compound satisfying the chemical formula (5) include:

Etc.

Hereinafter, R ⁶ —COOH, a proton acid satisfying the chemical formula (4) or the chemical formula (5) is referred to as a proton acid (small), and other proton acids are referred to as proton acids (large).

  The blending amount of the protonic acid (D) is preferably 1 part by weight or more and more preferably 5 parts by weight or more with respect to 100 parts by weight of the rubber component (A). If the amount of the protonic acid (D) is less than 1 part by weight, there is a tendency that it is not sufficient to react with the nitrogen compound (B). Further, the blending amount of the protonic acid (D) is preferably 20 parts by weight or less, and more preferably 10 parts by weight or less. When the blending amount of the protonic acid (D) exceeds 20 parts by weight, crosslinking tends to be inhibited.

  As a combination of imidazoles and protonic acid (D), a combination of imidazoles (II) and protonic acid (large) is not preferable because steric hindrance is large and hydrogen bonds cannot be obtained effectively. Any combination of imidazoles (I) and proton acids (small), imidazoles (II) and proton acids (small), imidazoles (I) and proton acids (large) is preferred. In consideration of steric hindrance, the combination of imidazoles (I) and protonic acids (small) is most preferable.

  In addition, the rubber composition of the present invention preferably contains a reinforcing filler.

  Examples of reinforcing fillers include carbon black, silica, calcium carbonate, magnesium carbonate, calcium hydroxide, magnesium hydroxide, aluminum hydroxide, talc, and clay. Black is preferred.

The nitrogen adsorption specific surface area (N ₂ SA) of carbon black is preferably 80 m ² / g or more, and more preferably 100 m ² / g or more. When N ₂ SA of carbon black is less than 80 m ² / g, grip performance and wear resistance tend to decrease. Further, N ₂ SA of carbon black is preferably 280 m ² / g or less, and more preferably 200 m ² / g or less. When N ₂ SA of carbon black exceeds 280 m ² / g, workability tends to be lowered.

  When carbon black is contained as a reinforcing filler, the content of carbon black is preferably 10 parts by weight or more, more preferably 20 parts by weight or more with respect to 100 parts by weight of the rubber component (A). When the content of carbon black is less than 10 parts by weight, the wear resistance tends to decrease. The carbon black content is preferably 200 parts by weight or less, and more preferably 150 parts by weight or less. When the content of carbon black exceeds 200 parts by weight, processability tends to be lowered.

  The rubber composition for tires of the present invention preferably further contains oil.

  Examples of the oil include process oils such as aroma oil, naphthenic oil, and paraffin oil, and oils derived from natural resources such as vegetable oils.

  When oil is contained, the oil content is preferably 10 to 200 parts by weight, more preferably 20 to 150 parts by weight, including the oil-extended oil, with respect to 100 parts by weight of the rubber component (A). If the oil content is less than 10 parts by weight, the wet grip performance tends to be insufficient, and if it exceeds 150 parts by weight, the wear resistance tends to be remarkably reduced.

  The rubber composition for tires of the present invention preferably further contains a tackifying resin.

  Examples of the tackifying resin include coumarone resin, phenolic resin, terpene resin, and xylene resin.

  The softening point of the tackifying resin is preferably 40 to 200 ° C, more preferably 60 to 180 ° C. When the softening point of the tackifying resin is less than 40 ° C., the grip performance under a high temperature condition tends to decrease, and when it exceeds 200 ° C., the dispersibility during kneading tends to decrease.

  When the tackifying resin is contained, the content of the tackifying resin is preferably 1 to 50 parts by weight and more preferably 5 to 30 parts by weight with respect to 100 parts by weight of the rubber component (A). If the content of the tackifying resin is less than 1 part by weight, there is a tendency that sufficient grip performance cannot be obtained, and if it exceeds 50 parts by weight, excessive tackiness is exhibited and processing tends to be difficult.

  In addition to the rubber component (A), nitrogen compound (B), organometallic compound (C), protonic acid (D), reinforcing filler, oil, and tackifying resin, Compounding agents used in the rubber industry, for example, various anti-aging agents, vulcanizing agents such as stearic acid, zinc oxide and sulfur, various vulcanization accelerators and the like can be appropriately mixed.

  The rubber composition of the present invention is used for tires, and particularly excellent in both low temperature grip performance and high temperature grip performance, and therefore is suitably used as a tread among tire members.

  The tire of the present invention is produced by a usual method using the rubber composition of the present invention as a tread. That is, the rubber composition is extruded into a tread shape at an unvulcanized stage and bonded together with other tire members on a tire molding machine by an ordinary method to form an unvulcanized tire. The unvulcanized tire can be heated and pressurized in a vulcanizer to obtain the tire of the present invention.

  Examples of tires include passenger car tires and competition tires, but competition tires are preferred because particularly excellent grip performance can be obtained.

  The present invention will be specifically described based on examples, but the present invention is not limited to these examples.

Hereinafter, various chemicals used in Examples , Reference Examples and Comparative Examples will be described together.
Styrene butadiene rubber (SBR): Toughden 4350 manufactured by Asahi Kasei Co., Ltd. (amount of bound styrene: 39% by weight, containing 50 parts by weight of oil with respect to 100 parts by weight of rubber solids)
Carbon black: Dia Black A (N110, N ₂ SA: 130 m ² / g) manufactured by Mitsubishi Chemical Corporation
Nitrogen compound (small): 2-methylimidazole manufactured by Nippon Synthetic Chemical Co., Ltd. (see imidazoles (I), chemical formula (6))

Nitrogen compound (large): Curesol C2E4MZ-A (2,4-diamino-6- (2-ethyl-4-methyl-1-imidazolylethyl) -1,3,5-triazine manufactured by Shikoku Kasei Kogyo Co., Ltd. Imidazoles (II), see chemical formula (7))

Organometallic compound: Magnesium acetate protonic acid (large) manufactured by Kishida Chemical Co., Ltd .: 4,4′-butylidenebis- (3-methyl-6-tert-butylphenol) (see chemical formula (8))

Protic acid (small): 2,6-di-tert-butyl-4-ethylphenol (see chemical formula (9))

Anti-aging agent 6C: Santoflex 13 (N-phenyl-N ′-(1,3-dimethylbutyl) -p-phenylenediamine) manufactured by Flexis
Anti-aging agent 224: Nocrack 224 (2,2,4-trimethyl-1,2-dihydroquinoline polymer) manufactured by Flexis
Stearic acid: Nippon Oil & Fats Co., Ltd. Zinc Oxide: Mitsui Metal Mining Co., Ltd. Zinc Oxide Type 2 Aroma Oil: Japan Energy Co., Ltd. Process X-260
Tackifying resin: Neopolymer 140 manufactured by Nippon Petrochemical Co., Ltd. (softening point: 140 ° C.)
Sulfur: Powdered sulfur vulcanization accelerator manufactured by Tsurumi Chemical Industry Co., Ltd .: Noxeller NS (N-tert-butyl-2-benzothiazolylsulfenamide) manufactured by Ouchi Shinsei Chemical Industry Co., Ltd.

Example 2, Reference Examples 1 and 3-8 and Comparative Examples 1-3
According to the formulation shown in Table 1 and Table 2, using a BP Banbury mixer, the mixture was kneaded for 3 minutes at 150 ° C. to obtain a kneaded product. Next, sulfur and a vulcanization accelerator were added to the obtained kneaded material, and kneaded for 5 minutes under the condition of 50 ° C. using an open roll to obtain an unvulcanized rubber sheet. Furthermore, the obtained unvulcanized rubber sheet was press-vulcanized for 12 minutes at 170 ° C., and vulcanized rubber sheets of Example 2, Reference Examples 1 and 3 to 8 and Comparative Examples 1 to 3 were produced. In the following evaluation results, Comparative Example 1 was used as the reference composition in Table 1, and Comparative Example 2 was used as the reference composition in Table 2.

(Degree of crosslinking (SWELL))
The obtained vulcanized rubber sheet was extracted with toluene, and the volume change rate (SWELL) before and after extraction was measured. In addition, it shows that the dispersion | variation in bridge | crosslinking can be suppressed and it is so preferable that SWELL is small.

(Viscoelasticity test)
Using a viscoelastic spectrometer manufactured by Iwamoto Seisakusho Co., Ltd., viscoelasticity (complex elastic modulus) of a vulcanized rubber sheet at 40 ° C. and 100 ° C. under conditions of initial strain of 10%, dynamic strain of 2%, and vibration frequency of 10 Hz. E ′ and loss tangent tanD) were measured. In both the viscoelasticity test at 40 ° C. and the viscoelasticity test at 100 ° C., the larger E ′, the higher the rigidity and the better, and the larger tan δ, the higher the grip force and the better the grip performance. It shows that.

(Tensile test)
In accordance with JIS K 6251 “Vulcanized Rubber and Thermoplastic Rubber-Determination of Tensile Properties”, a tensile test was conducted using a No. 3 dumbbell-shaped rubber test piece made of the vulcanized rubber sheet, and the stress at 300% elongation ( M300) was measured. Then, the tensile strength index of the reference blend was set to 100, and M300 of each blend was displayed as an index by the following formula. In addition, it shows that it is excellent in abrasion abrasion resistance, so that a tensile strength index | exponent is large.
(Tensile strength index) = (M300 of each formulation) / (M300 of standard formulation) × 100

(Actual vehicle evaluation)
The unvulcanized rubber sheet is formed into a tread shape, bonded to another tire member, and press vulcanized at 170 ° C. for 12 minutes to obtain a test cart tire (size: 11 × 7.10− 5) was produced.

  The manufactured cart tire was mounted on a test cart, and the test course of 2 km per lap was run for 8 weeks. The grip performance of the reference blended tire was 3 points, and the test driver made a sensory evaluation with a maximum score of 5 points. The initial grip performance indicates the grip performance of the first to fourth laps, and the second half grip performance indicates the grip performance of the fifth to eighth laps. Furthermore, the tire appearance of the reference blend after running was given 3 points, and the wear appearance of each blend was evaluated relative to a maximum of 5 points.

  The evaluation results of the test are shown in Tables 1 and 2.

Claims (4)

(A) Group consisting of 0.1 to 30 parts by weight of a nitrogen compound, (C) 0.1 to 30 parts by weight of an organometallic compound, and (D) a phenolic compound with respect to 100 parts by weight of the rubber component A rubber composition containing 1 to 20 parts by weight of at least one protonic acid selected from
The nitrogen compound (B) has the chemical formula (2):

( Wherein R ² is a monovalent chain hydrocarbon group, R ³ is —NH ₂ , R ⁴ is a divalent chain hydrocarbon group, and X is a cyclic structure containing d nitrogen atoms) X may include a double bond, b is an integer of 0 to 3, c is an integer of 0 to 5, d is an integer of 1 to 6, b R ² , c R ³ in each may be the same or different, and d N may be adjacent or not adjacent )
In represented imidazoles one or more der Louis imidazole compound is selected from the group consisting of (II) and (II), formula (1):

(In the formula, R ¹ is a monovalent chain hydrocarbon group, a is an integer of 0 to 4, a R ^{1 s} may be the same or different, and the total carbon number of R ¹ is 10 Is the following)
A mixture with one or more imidazoles (I) selected from the group consisting of imidazoles (I) represented by:
Phenolic compounds

A rubber composition. The rubber composition according to claim 1, further comprising 10 to 200 parts by weight of carbon black. The rubber composition according to claim 1 or 2, further comprising 1 to 50 parts by weight of a tackifying resin having a softening point of 40 to 200 ° C. A tire using the rubber composition according to claim 1, 2 or 3.