JPH0572409B2 - - Google Patents

Description

[Detailed description of the invention]

The present invention relates to a method for producing a rubber composition for a tire tread, and in particular a method for producing a rubber composition suitable for a tread for a racing tire. More specifically, the present invention relates to a method for producing a rubber composition suitable for treads for racing tires, which has excellent durability and is obtained by using a wet process carbon black masterbatch. When obtaining a rubber composition, carbon black (hereinafter simply referred to as CB) is often added and kneaded in order to increase the hardness, tensile strength, and tear or peel strength of the final product. . When adding CB to rubber substances,
Fine particles of CB must be uniformly dispersed and mixed into the rubber material. To perform such mixing,
Conventionally, CB is mixed with rubber and other ingredients in a Banbury mixer, or CB is added and kneaded with other ingredients to rubber that is being kneaded on a roll mill. These mixing methods are usually called dry mix methods, and are currently the most widely used method for blending and dispersing CB in the rubber industry. By using this dry mix method, ordinary
CB is well dispersed at a practical level and is widely used as a rubber composition for general purposes. However, when changing the CB to be added from the commonly used particle size range to a significantly smaller particle size, especially CB called ultrafine particle CB,
(In other words, the value of the specific surface area indicated by the amount of nitrogen adsorption has increased), specifically, the grade of CB is N-110 (N-110 is the name called ASTM, -110 has a specific surface area of 135 m ² /g) or more, and when it comes to CB with a fine particle size,
CB at a practical level in the normal dry mix method
Dispersion is not easily reached. That is, in general,
As the nitrogen adsorption specific surface area (SN ₂ , hereinafter referred to as SN ₂ ) increases, the tensile strength (TB, hereinafter referred to as TB) increases.
increases, but the degree of dispersion of CB begins to decrease rapidly. The increase in TB stops around SN ₂ = 120, and when SN ₂ exceeds 120, TB tends to decrease. In this case, it is necessary to input energy that exceeds the kneading energy normally considered.
To avoid this, some improvement can be made by increasing the kneading process into multiple stages, but this is not a fundamental solution. Furthermore, in the case of racing tire treads, due to their special performance requirements, a rubber composition that combines so-called high styrene styrene-butadiene rubber (SBR) with a bound styrene content of 30% or more and CB with a small particle size is used. Often used. Normally, as the kneading of SBR progresses, the viscosity of SBR decreases due to temperature rise or molecular cleavage. High styrene SBR
Compared to standard SBR (approximately 23.5% bound styrene content), the viscosity decreases more rapidly during kneading. Therefore, when using a CB whose dispersion progresses in the presence of shear stress, the dispersibility of the CB is significantly reduced. In addition to the above-mentioned problems with treaded racing tires, in order to improve the limit performance,
This requires CB with a particle size that is unimaginable for ordinary tire treads, which creates even more adverse conditions for CB dispersion. Particularly in certain types of racing tires, _SN2
Ultrafine particle CB of 150m ² /g or more, about 200m ² /g
is often used, and in this case the kneading is done by CB
Requires careful attention and extensive kneading for dispersion. As mentioned above, the dry mix method, which is economically disadvantageous due to the difficult problems described above, has a CB dispersion level that is considered to be possible with ordinary tire tread rubber compositions even if it is kept in the best possible state. A dispersion degree of only a few percent to several tens of percent was achieved, which shows how CB dispersion was a limiting factor in improving the performance of rubber compositions. Additionally, one of the basic physical properties required of racing tires is energy loss or hysteresis loss between the tire tread and the road surface, and the larger this is, the better the maneuverability and stability of a car equipped with the tire will be. . For a given rubber type, carbon black type, amount of carbon black added, and amount of oil (aromatic process oil) added, in order to maximize the above energy loss, the interaction between CB and rubber must be maximized. However, in the conventional dry mix method, when blending CB with SN ₂ = 120 m ² /g or more,
Poor dispersion of CBs, that is, agglomeration of CBs tends to occur,
As mentioned above, a CB with a high SN _binary value cannot be used effectively. Against this background, the inventors of the present invention have developed a method that is reasonable in place of the dry mix method using high styrene SBR and ultrafine particle CB, which has many disadvantages as mentioned above and is also economically disadvantageous. We have completed various studies to find a suitable CB dispersion method, and have completed the present invention. That is, the present invention uses ultrafine particle CB as a filler that satisfies the physical properties required for tire treads, especially racing tire treads, and disperses it well in a rubber material to maintain good strength and wear resistance. The purpose of the present invention is to provide a method for producing a rubber composition that is particularly effective for use in racing tire treads, and which has improved energy loss between contact with the road surface when used as a tire. (a) Rubber latex containing 70% by weight or more of a diene rubber component with a solid content of 100%
parts by weight, (b) an amount of carbon black slurry obtained by dispersing carbon black with a nitrogen adsorption specific surface area of 120 to 200 m ² /g in water, in a solid content of more than 150 parts by weight, and (c) aromatic process oil. A coagulant is added to the mixture obtained by mixing and/or a high viscosity oil in an amount of more than 110 parts by weight, and the coagulant is coagulated, and the dried coagulate is added to the mixture in a proportion of more than 110 parts by weight of the rubber component. A method for producing a rubber composition for tire treads, which comprises blending 5 to 30 parts by weight of carbon black and 0 to 30 parts by weight of an aromatic process oil and/or a high viscosity oil. The present invention will be explained in detail below. The diene rubber latex in the method of the present invention is prepared by emulsifying and dispersing 1,3-butadiene monomer or 1,3-butadiene monomer and styrene monomer in an aqueous medium using an emulsifier, and then adding a polymerization initiator. It is produced by a conventionally known method of causing a polymerization reaction. As the emulsifier used, anionic surfactants such as fatty acid soap, rosin acid soap, sodium naphthalene sulfonate formalin condensate, and sodium alkylbenzesulfonate are usually used. As a polymerization initiator, a persulfate such as potassium persulfate is used in a so-called hot rubber formulation in which polymerization is carried out at a high temperature of 30 to 60°C, and a redox initiator is used in a cold rubber formulation in which polymerization is carried out at a temperature of 0 to 20°C. As a redox initiator, a combination of an organic peroxide such as cumene hydroperoxide, diisopropylbenzene hydroperoxide, or para-menthane hydroperoxide and ferrous sulfate is generally used, and as a reducing agent, sulfoxylate, etc. are used together. Furthermore, when an emulsion polymerized polybutadiene (EBR) latex is obtained using only 1,3-butadiene, nitrobenzene may be added to the polymerization system to improve linearity. When polybutadiene rubber or styrene-butadiene rubber is obtained by ordinary emulsion polymerization, when the polymerization reaction rate reaches 55 to 65% [polymerization reaction rate 65%
If the concentration is above, branching occurs in the main chain of the polymer (becoming a high molecular weight component), and roll processability (wrapability) is significantly reduced. Stop the reaction. A polybutadiene rubber latex can be obtained by stripping unreacted monomers using steam or the like. The rubber latex used in the method of the present invention contains a diene rubber component of 70% by weight or more (percentage as solid content), and if the amount is less than this, the dispersibility of CB will be poor and the abrasion resistance will decrease. do.
Other than diene rubber components, natural rubber, ethylene-
It may also contain propylene rubber. In addition, as a rubber latex containing a diene rubber component, use a combination of SBR, especially high styrene SBR latex, and polybutadiene rubber (EBR) latex [SBR/EBR = 80/20 to 20/80 (solid content weight ratio)]
By doing so, wear resistance can be improved. The rubber latex obtained as described above contains the ultrafine CB particles, that is, CB with an SN ₂ of 120 to 200 m ² /g.
[Ratio of more than 150 parts by weight and less than 250 parts by weight (solid content) of the latter for 100 parts by weight of the former] and aromatic processing oil and/or high Make a CB rubber latex masterbatch by mixing viscosity oil (more than 100 parts by weight and less than 200 parts by weight per 100 parts by weight of rubber latex solid content). In this case, the CB to be mixed is added to the rubber latex in the form of an aqueous dispersion (slurry). As the aqueous dispersion of CB, it is preferable to use a so-called dispersion method in which CB is added to water and stirred at high speed to form a CB slurry. In other words, if the agitation is weak, the water may be difficult to absorb into the CB. For example, U.S. Patent No.
It is preferable to carry out the method described in No. 2769795. The CB-rubber latex masterbatch obtained by mixing the rubber latex, CB slurry, aromatic process oil and/or high viscosity oil as described above is coagulated with an acid such as sulfuric acid, and then washed with water, filtered and dried. A carbon black masterbatch (hereinafter abbreviated as W-CBMB) is obtained by the wet method. For the W-CBMB obtained in this way,
For 100 parts by weight of the rubber component of this product, CB5 to 30
parts by weight (the CB used in this case is not particularly limited, but it is better to use a CB with a nitrogen adsorption specific surface area of 120 to 200 m ² /g) and 0 to 30 parts by weight of aromatic process oil and/or high viscosity oil If necessary, compounding agents commonly used in this field are added, kneaded in a Banbury mixer, and vulcanized in a conventional manner. In the composition of the present invention, the blending ratios of the rubber component, CB component, and oil components such as process oil when preparing W-CBMB and preparing the final composition from this were determined for the following reasons. be. In other words, automobile tires must have a good balance of functions such as running performance, ride comfort, and stability, and each rubber composition for tires has a role to play, and the amount of each added must be adjusted accordingly. By changing the tire performance, a subtle difference is created in the balance of the tire performance. For example, as the amount of CB increases, the tire becomes harder and the ride quality of the car becomes worse. Also, adding more oil will make the tires softer and make the ride more comfortable. However, if the oil is added too much, the wear resistance will be drastically reduced. Furthermore, as the amount of sulfur increases, the tires become harder and ride comfort decreases. Taking these various factors into consideration, in the present invention, the proportions of each compounded component were determined so as to obtain a tire tread rubber composition suitable for racing use. As described above, according to the present invention, ultrafine particles, that is, CB with a large specific surface area are used, and by a wet method,
By mixing with rubber components and other compounding components to create a masterbatch, we can achieve good CB dispersion with fewer steps and less kneading energy than conventional dry mix methods, and improve wear resistance, blowout properties, etc. with excellent properties in
It is possible to obtain a rubber composition suitable for a racing tire tread, which, when made into a tire, has a large energy loss with respect to the road surface and provides stable maneuverability. Next, Examples and Comparative Examples of the present invention will be shown. Various physical properties of the rubber compositions obtained in these Examples and Comparative Examples were measured and shown in Table 1 below. Each item in this table was measured by the following method. The degree of dispersion of CB was measured using a Leitz microtome (Leitz).
(manufactured by). Tanδ, which indicates viscoelastic properties, was measured using a viscoelastic spectrometer (manufactured by Iwamoto Seisakusho) at a temperature of 23
The mechanical loss tangent (tan δ) was determined at °C, frequency 10 Hz, and strain 5%. Repulsion elasticity is measured according to JIS K-6301 using the Ryupke method (pendulum impact method). Abrasion resistance is Akron abrasion (BS standard 903Part
A9C) and pico wear (ASTM D2228) were both measured. The former was measured using an Akron abrasion tester (manufactured by Ueshima Seisakusho), and the latter was measured using a Pico abrasion tester (manufactured by Ferry Machine). The wet skid resistance value (index) is measured using a portable wet skid tester (UK).
Measured using Safety Walk Type B manufactured by Stanley, road surface: Safety Walk Type B manufactured by Sumitomo 3M, water temperature 20°C). The blowout characteristics were measured using a Gutsudoritsu flexometer (manufactured by Ueshima Seisakusho), and the conditions were a temperature of 100°C.
°C, stroke 5.72mm, load 62 lbs (28.1Kg),
The test was carried out for 7 minutes, and the cross section of the cut was evaluated as follows. That is, a five-level evaluation was performed, with cracks occurring as 1, small holes occurring as 3, no holes occurring as 5, and 2.
and 4 are evaluated as intermediate values. Power consumption indicates the amount of power consumed by OOC type Banbury mixer operation, the first stage power consumption is the power consumption for kneading a compound system that does not contain a vulcanizing agent, and the second stage power consumption is for kneading a compound system that contains a vulcanizing agent. Indicates power consumption. Example 1 Styrene monomer as the 1,3-butadiene monomer was emulsified and dispersed in an aqueous medium using a mixed emulsifier of fatty acid soap and rosin acid soap, and the polymerization initiator was para-menthane hydroperoxide and primary sulfuric acid. Polymerization was carried out below 10°C using a combination of iron and sodium formaldehyde sulfoxylate as a reducing agent. In this way, the amount of bound styrene
Got an SBR of 40%. This styrene-butadiene rubber latex 100
Aromatic process oil by weight (as solids)
190 parts by weight and carbon black N110 [SN ₂ is
135 m ² /g, dibutyl phthalate (hereinafter abbreviated as DBP) oil absorption 116 ml/100 g] 180 parts by weight was dispersed in water using the ultra-dispersion method (according to the method described in US Patent No. 2,769,795) to form a CB slurry. Add to the mixture, mix well at 50-70℃, coagulate with sulfuric acid, wash with water, filter, and heat to 100~70℃.
Dry at 120℃. 10 parts by weight of CB (N110), 1.0 parts by weight of stearic acid, and 3.0 parts by weight of zinc oxide were added to the W-CBMB thus obtained in proportion to 100 parts by weight of the rubber component in this W-CBMB, and OOC Type Banbury mixer [circulating water temperature 70℃, rotor rotation speed
54.5 (front)/62.5 (rear) rpm], the kneaded mixture was cooled with a 10 inch (25.4 cm) roll,
It was made into a sheet. Sulfur 1.75 in the rubber sheet thus obtained
Parts by weight and vulcanization accelerator (Sanshin Kagaku Co., Ltd. Sunceller NOB, active ingredient N-oxydiethylene-2-
2.0 parts by weight of benzothiazyl sulfenamide) was added and kneaded using the same OOC type Banbury mixer as above, and then the kneaded product was cooled with a 10-inch roll and formed into a sheet. Form this rubber sheet,
Vulcanization was performed at 155°C for 30 minutes using a super press. The physical properties of this product are shown in Table 1 below. Example 2 SN ₂ as CB is 187m ² /g, DBP oil absorption is 122
A rubber composition was obtained in the same manner as in Example 1 except that ultrafine particles CB of ml/100g were used. The physical properties of this product are shown in Table 1. Comparative Example 1 These conventional dry mix methods were used. A high styrene SBR latex was obtained from 1,3-butadiene and styrene in the same manner as in Example 1, and 37.5 parts by weight of aromatic process oil was added to this SBR latex based on 100 parts by weight of the solid content. Mix at 50-70°C, coagulate with sulfuric acid, wash with water, filter, and dry at 100-120°C. Process oil-containing SBR obtained in this way
Based on 100 parts by weight of the rubber component of this product,
CB (N339) (SN ₂ is 88m ² /g, DBP oil absorption 123
ml/100g) 190 parts by weight and aromatic process oil
142.5 parts by weight are blended in the following proportions. In other words, the final total blending amount is 190 parts by weight of CB, 180 parts by weight of process oil.
Make sure it is by weight. First, the rubber component 100% is added to SBR containing process oil.
1/2 of the total blended amount of CB and process oil, 1.0 parts by weight of stearic acid and 3.0 parts by weight of zinc oxide are mixed in an OOC type Banbury mixer in proportion to parts by weight, and the mixture is cooled with a 10-inch roll to form a sheet. become The remaining CB is added to the rubber sheet obtained in this process.
and process oil are similarly kneaded using an OOC type Banbury mixer, and this mixture is cooled and formed into a sheet using a 10-inch roll. This sheet was similarly OOCed with 1.75 parts by weight of sulfur and 2.0 parts by weight of a vulcanization accelerator (Suncera NOB).
Knead with a type Banbury mixer and mix this kneaded material with 10
Cool with inch rolls and form into sheets. Next, this rubber sheet was molded and vulcanized using a hot press at 155°C for 20 minutes. The physical properties of this product are shown in Table 1. Comparative Example 2 Similar to Example 1, this example uses the wet mix method to produce W-CBMB, but the CB used in Comparative Example 1 is a CB with the same SN ₂ of 88 m ² /g.
(N339), and everything else was carried out in the same manner as in Example 1. Table 1 shows the physical properties of the obtained rubber composition. Comparative Example 3 In this example, like Comparative Example 1, CB is mixed by the dry mix method, but CB (N220)
(SN ₂ is 104m ² /g, DBP oil absorption is 115ml / 100g)
The same procedure as in Comparative Example 1 was carried out in all other respects. Table 1 shows the physical properties of the obtained rubber composition. Comparative Example 4 Similar to Example 1, this example uses the wet mix method to produce W-CBMB, but the CB used in Comparative Example 3 is CB with an SN ₂ of 104 m ² /g.
(N220), and everything else was carried out in the same manner as in Example 1. Table 1 shows the physical properties of the obtained rubber composition. Comparative Example 5 In this example, like Comparative Example 1, CB is mixed by the dry milk method, except that Example 1 is used as CB.
CB (N110) with SN ₂ of 135 m ² /g, same as used in
The same procedure as in Comparative Example 1 was carried out in all other respects.
Table 1 shows the physical properties of the obtained rubber composition. Comparative Example 6 This example was carried out in the same manner as Comparative Example 1, but with CB
, the same SN ₂ used in Example 2 is 187
Ultrafine CB particles of m ² /g were used. Table 1 shows the physical properties of the obtained rubber composition.

[Table] In Tables 1 and 2 above, in the mixing method column, dry means dry mix method, and wet means CB as in the method of the present invention.
A method in which rubber latex is mixed with rubber latex in the form of an aqueous slurry. From the above table, it is clear that the method of the present invention is superior in all aspects, including the physical properties of the resulting composition and the power consumption during production. What has been explained above and mentioned in the examples is related to typical illustrations to help the understanding of the present invention, and the present invention is not limited by these illustrations, and other examples may be used within the gist of the invention. Modifications can be made.

Claims (1)

[Claims] 1. (a) 100 parts by weight of rubber latex containing a diene rubber component of 70% by weight or more, (b) Carbon black with a nitrogen adsorption specific surface area of 120 to 200 m ² /g in water. In a mixture obtained by mixing the carbon black slurry obtained by dispersion in an amount of more than 150 parts by weight in terms of solid content, and (c) an aromatic process oil and/or a high viscosity oil in an amount of more than 110 parts by weight. A coagulant is added and coagulated, and the coagulated product is dried, and 5 to 30 parts by weight of carbon black and 0 to 30 parts by weight of aromatic process oil and/or high viscosity oil are added to this product in proportion to 100 parts by weight of the rubber component. A method for producing a rubber composition for tire tread, which comprises blending the following. 2. The method for producing a rubber composition for tire treads according to claim 1, wherein the diene rubber component of the rubber latex is styrene-butadiene rubber containing 15 to 50% by weight of bound styrene. 3. Rubber latex contains 15-50% by weight of bound styrene.
Claim 1 contains a styrene-butadiene rubber latex and a polybutadiene rubber latex obtained by an emulsion polymerization method.
A method for producing a rubber composition for tire leads as described in 2.