Rubber composition for tire

BACKGROUND OF THE INVENTION
The present invention relates to a rubber composition, for a tire, which can improve tire durability.
Blending of polybutadiene rubber, use of carbon black having a small particle diameter, EV (effective vulcanization), use of a semi-EV type vulcanization accelerator and the like have hitherto been attempted to enhance the abrasion resistance of a rubber composition for a tire tread and thereby improve the durability of the tire. These means, however, generally deteriorate the wet performance, heat build-up, fracture properties and other properties, and it has been difficult to significantly improve the abrasion resistance while minimizing the influence on such other properties.
Further, good crack resistance is required of rubber compositions for a side wall, a rim cushion, or an inner liner of a tire, and there is a demand for use of a rubber composition having excellent fatigue resistance in a belt layer, a carcass layer, or a bead filler. Up to now, however, no rubber composition having satisfactory crack resistance and fatigue resistance has been proposed in the art.
SUMMARY OF THE INVENTION
An object of the present invention is to provide a rubber composition, for a tire, which can improve the abrasion resistance without sacrificing the wet performance (wet road grip force), fracture properties, and heat build-up and, at the same time, has enhanced crack resistance and fatigue resistance and, hence, can improve the tire durability.
According to the present invention, the above object can be attained by a rubber composition for a tire, comprising at least one compound selected from the group consisting of ascorbic acid and derivatives thereof, tocopherols, and citric acid and derivatives thereof.
The use of this rubber composition in a tire tread results in improved abrasion resistance of the tread without substantially sacrificing wet performance, fracture properties, and heat-build up, enhancing the tire durability.
Further, the use of the above rubber composition in a side wall, a rim cushion, and/or an inner liner results in improved crack resistance of these sections of the tire, enhancing the tire durability.
Furthermore, the use of above rubber composition in a belt layer, a carcass layer, and/or a bead filler of the tire results in improved fatigue resistance of these sections of the tire, enhancing the tire durability.

BRIEF DESCRIPTION OF THE DRAWING
FIG. 1 is a meridian half cross-sectional view of one embodiment of each section constituting a tire using the rubber composition for a tire according to the present invention.

DESCRIPTION OF THE PREFERRED EMBODIMENTS
One embodiment of each section constituting a tire using the rubber composition for a tire according to the present invention is shown in FIG. 1. In FIG. 1, a tire T comprises a pair of right and left bead sections 1, a pair of right and left side walls 2, and a tread 3 extending to both the side walls. A carcass layer 4 is provided between the bead sections 1,1, and the end portion of the carcass layer 4 is folded back and wound up around a bead core 5 and a bead filler 6 from the inner side of the tire towards the outer side of the tire. In the tread 3, a belt layer 7 is disposed on the outer side of the carcass layer 4 over one round of the tire. An inner liner 8 is provided over the surface of inside of the tire T to prevent air filled in the interior of the tire from being leaked out. A rim cushion 9 comprising a rubber composition having relatively high hardness is disposed in the bead section 1 in its portion in contact with the rim.
The rubber composition for a tire according to the present invention may be used to constitute the tread 3, the side wall 2, the rim cushion 9, the inner liner 8, the belt layer 7, the carcass layer 4, and/or the bead filler 6.
The ascorbic acid and its derivatives according to the present invention are compounds represented by the following formula (1). Examples thereof include ascorbic acid (vitamin C) represented by the following formula and an ester of ascorbic acid with a carboxylic acid, that is, ascorbyl stearate or ascorbyl palmitate. A salt of ascorbic acid with an alkali metal or an alkaline earth metal (for example, magnesium ascorbate represented by the following formula) may also be used. In the rubber composition, the metal salt reacts with an acid, such as stearic acid, to return to ascorbic acid. ##STR1##
(R represents any group) ##STR2##
Tocopherols include, for example, .alpha.-tocopherol (vitamin E) represented by the following formula (2), .beta.-tocopherol, .gamma.-tocopherol, .delta.-tocopherol, .xi..sub.2 -tocopherol, and .eta.-tocopherol represented by the following formulae, .epsilon.-tocopherol represented by the following formula (3), and .xi..sub.1 -tocopherol represented by the following formula. ##STR3## (wherein R.sub.1 represents a part of skeleton) ##STR4## wherein R.sub.1 represents a part of skeleton) ##STR5##
Citric acid and its derivatives are represented by the following formula (4), and examples thereof include citric acid represented by the following formula and an ester of citric acid with an alcohol, such as triallyl citrate. A salt of citric acid with an alkali metal or an alkaline earth metal (for example, magnesium citrate represented by the following formula) may also be used. In the rubber composition, the metal salt can react with an acid, such as stearic acid, to return to citric acid. ##STR6## (wherein R.sub.2, R.sub.3 , and R.sub.4 which may be the same or different represent any group and has a bond between these groups) ##STR7##
The rubber composition for a tire according to the present invention comprises at least one compound selected from the group consisting of the above ascorbic acid and derivatives thereof, tocopherols, and citric acid and derivatives thereof. The at least one compound may be selected independently of the optical activity, and any of d form, L form, and dL form may be used. The content of the at least one compound may be 0.05 to 5 parts by weight, preferably 0.5 to 4 parts by weight, based on 100 parts by weight of a diene rubber or a halogenated butyl rubber. When the content is less than 0.05 part by weight, the abrasion resistance, crack resistance, and fatigue resistance cannot be improved, while when it exceeds 5 parts by weight, vulcanization is unfavorably delayed.
The rubber composition used in the tire tread comprises, for example, 100 parts by weight of a diene rubber, 40 to 150 parts by weight of a carbon black, 0 to 150 parts by weight of a process oil, and 0.05 to 5 parts by weight of the above at least one compound.
The rubber composition used in the side wall, rim cushion, and/or inner liner comprises, for example, 100 parts by weight of a diene rubber or a halogenated butyl rubber, 20 to 130 parts by weight of a carbon black, 0.5 to 5 parts by weight of sulfur, and 0.05 to 5 parts by weight of the above at least one compound (particularly, vitamin C). In the case of the inner liner, the use of the halogenated butyl rubber is preferred from the viewpoint of preventing air within the tire from being leaked out.
The rubber composition used in the belt layer, carcass layer, and/or bead filler of the tire comprises, for example, 100 parts by weight of a diene rubber, 20 to 80 parts by weight of a carbon black, 1 to 10 parts by weight of sulfur, and 0.05 to 5 parts by weight of the above at least one compound (particularly, vitamin C).
The diene rubber is not particularly limited, and examples thereof include natural rubber (NR), styrene/butadiene copolymer (SBR), and polybutadiene (BR).
The halogenated butyl rubber also is not particularly limited, and examples thereof include brominated butyl rubber and chlorinated butyl rubber.
Preferably, the rubber composition for a tire according to the present invention further comprises a filler for rubber attached with at least one compound selected from particularly the above described ascorbic acid and its derivatives, tocopherols, and citric acid and its derivatives, when dispersion of the incorporated at least one compound can be facilitated and it is possible to attain the desired result with use of a relatively limited amount of such compound. In this connection, the solubility in rubber of for example the ascorbic acid is so low that if this acid is added directly in rubber, there tends to occur the problem of an insufficient or uneven dispersion, but normally it is that the desired result can be attained without a difficulty if the ascorbic acid is mixed in rubber at a high temperature in the vicinity of the melting point of the acid of 180.degree. to 190.degree. C. However, to add the ascorbic acid directly in rubber, itself, tends to affect the scorch acceleration, and it is not much advisable to mix the ascorbic acid with rubber at such a high temperature as above. In contrast to the above, if the ascorbic acid is added to rubber in the form of the acid being attached to a rubber-use filler as proposed above, it is possible even without raising the mixing temperature to realize a desirable dispersion of the ascorbic acid in rubber and obviate the need for worrying about deterioration of the scorch prevention.
The rubber filler may be any one commonly used for rubber and is not particularly limited. Examples thereof include carbon black, silica, and calcium carbonate.
The adhesion of the at least one compound to the filler for rubber may be performed, for example, by immersing a filler for rubber in a solution containing a dissolved ascorbic acid to coat the surface of the filler with the ascorbic acid. Preferably, the percentage adhesion of the at least one compound to the filler for rubber is 0.01 to 30% by weight based on the weight of the filler for rubber. When the percentage adhesion is less than 0.01% by weight, the effect of improving the abrasion resistance cannot be attained. On the other hand, when it exceeds 30% by weight, some of the at least one compound is present without being adhered to the filler, often posing problems associated with the scorch prevention, the dispersibility and/or the vulcanization rate or progress.
The filler for rubber incorporated may be 40 to 150 parts by weight, based on 100 parts by weight of a diene rubber, in total of the filler for rubber with the at least one compound adhered to thereto and a filler for rubber with the at least one compound not adhered thereto.
The content of the at least one compound (for example, an ascorbic acid compound, that is, ascorbic acid or its derivative) adhered to a filler for rubber is preferably 0.1 to 5 parts by weight based on 100 parts by weight of the diene rubber. When it is less than 0.1 part by weight, the abrasion resistance can not be improved, while when it exceeds 5 parts by weight, the vulcanization is unfavorably delayed.
For example, in the case of a tread for a pneumatic tire for running on a general road, at least one compound adhered to a filler for rubber may be incorporated in an amount of 0.1 to 1 part by weight based on 100 parts by weight of the diene rubber.
On the other hand, in the case of a tread for a pneumatic tire for running on an expressway, the ascorbic acid compound adhered to a filler for rubber may be incorporated in an amount of 0.1 to 5 parts by weight based on 100 parts by weight of the diene rubber.
The present invention will be described with reference to the following examples comparatively with comparative examples, though the invention is not limited to these examples only.
EXAMPLES AND COMPARATIVE EXAMPLES
(1) Formulation ingredients (in parts by weight) specified in Table 1 were mixed and kneaded together by means of a Banbury mixer and a mixing roll according to a conventional method to prepare various rubber compositions (Examples 1 to 9 and Comparative Example 1). These rubber compositions were press-vulcanized at 160.degree. C. for 20 to 50 min, thereby preparing test pieces for a tread which were then evaluated for wet performance, fuel economy, fracture properties, and abrasion resistance by the following methods. The results are given in Table 1.
Wet Performance:
A viscoelastic spectrometer manufactured by Toyo Seiki Seisaku Sho, Ltd. was used to measure tan .delta. at 0.degree. C. under conditions of distortion factor 10.+-.2% in stretch deformation and frequency 20 Hz. The larger the numerical value, the better the wet performance.
Fuel Economy:
A viscoelastic spectrometer manufactured by Toyo Seiki Seisaku Sho, Ltd. was used to measure tan .delta. at 60.degree. C. under conditions of distortion factor 10.+-.2% in stretch deformation and frequency 20 Hz. The smaller the numerical value, the better the fuel economy (the lower the rolling resistance).
Fracture properties:
The fracture properties were evaluated by measuring the tensile strength and the elongation at break. The larger the numerical value, the better the fracture properties (which means that fracture does not occur even upon larger deformation).
Method for measuring tensile strength:
The tensile strength was measured in accordance with the procedure set forth in JIS K6301 (tensile speed 500.+-.25 mm/min, testing temperature 23.+-.2.degree. C., load cell capacity such that the tensile strength falls within 15 to 85% of the capacity, JIS No. 3, and n=3).
Method for measuring elongation at break:
As with the tensile strength, the elongation at break was measured in accordance with the procedure set forth in JIS K6301.
Method for measuring abrasion resistance:
The abrasion resistance was determined by measuring Lambourn resistance under conditions of slip 25% and load 5 kg in accordance with the procedure set forth in JIS K6264. The results were expressed in terms of an index by taking the abrasion value in Comparative Example 1 as 100. The larger the numeral value, the better the abrasion resistance.
TABLE 1__________________________________________________________________________ Comp. Ex. 1 Ex. 2 Ex. 3 Ex. 4 Ex. 5 Ex. 6 Ex. 7 Ex. 8 Ex. 9 Ex. 1__________________________________________________________________________SBR 100 100 100 100 100 100 100 100 100 100Carbon black (SAF) 90 90 90 90 90 90 90 90 90 90Aromatic oil 53.0 53.0 53.0 52.6 52.6 52.6 52.8 52.8 52.8 55.0L-Ascorbic acid 1.0 2.0 4.0dl-.alpha.-Tocopherol 1.2 2.4 4.8Citric acid 1.1 2.2 4.4Zinc flower 3 3 3 3 3 3 3 3 3 3Stearic acid 2 2 2 2 2 2 2 2 2 2Vulcanization accelerator* 1.7 1.7 1.7 1.7 1.7 1.7 1.7 1.7 1.7 1.7Sulfur 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4Tensile strength, room temp./MPa 21.0 20.1 21.9 21.8 21.1 21.2 21.1 21.5 21.8 21.2Elongation at break, room temp./% 557 510 507 487 490 499 510 520 456 457Lambourn abrasion, 25% slipAbrasion resistance index (%) 107 112 137 102 104 106 103 102 113 100Load 5 kgStretch viscoelasticity 0.786 0.790 0.770 0.789 0.787 0.772 0.782 0.763 0.770 0.769tan .delta., 0.degree. C.Stretch viscoelasticity 0.409 0.394 0.402 0.397 0.385 0.399 0.409 0.399 0.402 0.400tan .delta., 60.degree. C.JIS hardness 67.4 68.8 67.4 70.6 70.0 68.8 69.4 70.2 68.4 71.2__________________________________________________________________________ Note) *: A mixture of Ncyclohexyl-2-benzothiazylsulfenamide with diphenylguanidine
As is apparent from Table 1, the rubber compositions of the present invention (Examples 1 to 9) are superior in abrasion resistance without sacrificing wet performance, fuel economy, and fracture properties to the rubber composition not containing the above at least one compound (Comparative Example 1). Among all the compounds used, the ascorbic acid is seen to be most effective.
In connection with representative rubber compositions for tires provided with use of the ascorbic acid, their physical properties were examined, and results of the examinations are shown in the following:
(2) Formulation ingredients (in parts by weight) specified in Table 2 were mixed and kneaded together by means of a Banbury mixer and a mixing roll according to a conventional method to prepare various rubber compositions (Examples 10 to 12 and Comparative Example 2). These rubber compositions were press-vulcanized at 160.degree. C. for 20 to 50 min, thereby preparing test pieces for a side wall which were then evaluated for crack resistance and processability by the following methods and, in addition, evaluated for fracture properties in the same manner as described in the above item (1). The results are given in Table 2.
Crack resistance:
(1) Before heat aging (flex cracking test)
The crack resistance before heat aging was determined by determining the crack growth upon repeated flexing with a de Mattia flexing tester in accordance with the procedure set forth in JIS K6301. The crack growth under conditions of stroke 57 mm, speed 300.+-.10 rpm, and 100,000 flexing cycles by taking the crack growth in Comparative Example 2 as 100. The larger the numerical value, the better the crack resistance.
(2) After heat aging (flex cracking test)
Heat aging was conducted in a gear oven at 80.degree. C. for 144 hr followed by determination of the crack growth in the same manner as described above in connection with the crack resistance before heat aging.
Processability:
The processability was evaluated by measuring the time taken for the viscosity to be increased by 5 Mooney at 125.degree. C. in accordance with the procedure set forth in JIS K6300. The smaller the numerical value, the better the processability.
TABLE 2______________________________________ Comp. Ex. 2 Ex. 10 Ex. 11 Ex. 12______________________________________NR 40 40 40 40BR 60 60 60 60Carbon black 50 50 50 50L-Ascorbic acid 0.5 1.0 2.0Aromatic oil 15.0 15.0 15.0 15.0Zinc flower 3.0 3.0 3.0 3.0Stearic acid 2.0 2.0 2.0 2.0Antioxidant-1 3.0 3.0 3.0 3.0Antioxidant-2 2.0 2.0 2.0 2.0Wax 1.5 1.5 1.5 1.5Sulfur 1.5 1.5 1.5 1.5Vulcanization accelerator 1.0 1.0 1.0 1.0Cracking resistanceFlex cracking testBefore heat aging 100 106 108 112After heat aging 75 86 88 91Processability 25 20 19 16Scorching time (min)Breaking propertiesTensile strength 8.0 7.8 7.6 7.3@ Room temp/MPaElongation at break 560 570 580 600@ Room temp./%______________________________________ Note) NR: SIR20 BR: Nipol 1220, manufactured by Nippon Zeon Co., Ltd. Carbon black: SEAST N (N.sub.2 SA = 74 m.sup.2 /g), manufactured by Tokai Carbon Co., Ltd. Aromatic oil: Process oil X140, manufactured by Kyodo Oil Co., Ltd. Zinc flower: Zinc flower No. 3, manufactured by Seido Chemical Industry Co., Ltd. Stearic acid: Lunac YA, manufactured by Kao Corp. Antioxidant1: NPhenyl-N(1,3-dimethyl)-p-phenylenediamine (Antigene 6C, manufactured by Sumitomo Chemical Co., Ltd.) Antioxidant2: Poly(2,2,4-trimethyl-1,2-dihydroquinoline) (Antigene RD, manufactured by Sumitomo Chemical Co., Ltd.) Wax: Sunnoc, manufactured by Ohuchi Shinko Chemical Industrial Co., Ltd. Sulfur: Oiltreated sulfur Vulcanization accelerator: NCyclohexyl-2-benzothiazolesulfenamide (Nocceler CZ, manufactured by Ohuchi Shinko Chemical Industrial Co., Ltd.
As is apparent from Table 2, the rubber compositions of the present invention (Examples 10 to 12) were superior in crack resistance to the rubber composition not containing ascorbic acid (Comparative Example 2).
(3) Formulation ingredients (in parts by weight) specified in Table 3 were mixed and kneaded together by means of a Banbury mixer and a mixing roll according to a conventional method to prepare various rubber compositions (Examples 13 to 15 and Comparative Example 3). These rubber compositions were press-vulcanized at 160.degree. C. for 20 to 50 min, thereby preparing test pieces for an inner liner which were then evaluated for crack resistance, processability, and fracture properties in the same manner as described in the above item (2). The results are given in Table 3.
TABLE 3______________________________________ Comp. Ex. 3 Ex. 13 Ex. 14 Ex. 15______________________________________IIR 75 75 75 75NR 25 25 25 25Carbon black 60 60 60 60L-Ascorbic acid 0.5 1.0 2.0Aromatic oil 4.0 4.0 4.0 4.0Zinc flower 3.0 3.0 3.0 3.0Stearic acid 1.0 1.0 1.0 1.0Sulfur 0.8 0.8 0.8 0.8Vulcanization accelerator 1.0 1.0 1.0 1.0Cracking resistanceFlex cracking testBefore heat aging 100 110 109 111After heat aging 57 77 80 84Processability 19 18 17 14Scorching time (min)Breaking propertiesTensile strength 8.0 7.8 7.6 7.4@ Room temp./MPaElongation at break 720 700 730 740@ Room temp./%______________________________________ Note) NR: SIR20 IIR: Brominated isobutylene isoprene rubber Carbon black: SEAST V (N.sub.2 SA = 27 m.sup.2 /g), manufactured by Tokai Carbon Co., Ltd. Aromatic oil: Process oil X140, manufactured by Kyodo Oil Co., Ltd. Zinc flower: Zinc flower No. 3, manufactured by Seido Chemical Industry Co., Ltd. Stearic acid: Lunac YA, manufactured by Kao Corp. Sulfur: Oiltreated sulfur Vulcanization accelerator: Dibenzothiazyl disulfide (Sanceler DM, manufactured by Sanshin Chemical Industry Co., Ltd.)
As is apparent from Table 3, the rubber compositions of the present invention (Examples 13 to 15) were superior in crack resistance to the rubber composition not containing ascorbic acid (Comparative Example 3).
(4) Formulation ingredients (in parts by weight) specified in Table 4 were mixed and kneaded together by means of a Banbury mixer and a mixing roll according to a conventional method to prepare various rubber compositions (Examples 16 to 18 and Comparative Example 4). These rubber compositions were press-vulcanized at 160.degree. C. for 20 to 50 min, thereby preparing test pieces for a belt layer which were then evaluated for fatigue resistance, initial adhesion, and adhesion after immersion in warm water by the following methods and, in addition, evaluated for processability and fracture properties in the same manner as described in the above item (2). The results are given in Table 4. For the evaluation of the initial adhesion and the adhesion after immersion in warm water, another test sample was provided.
Fatigue resistance:
(1) Strain-controlled fatigue life (before heat aging)
The strain-controlled fatigue life before heat aging was measured in accordance with the procedure set forth in JIS K6301, that is, by repeatedly applying a constant strain of 100% to a No. 3 dumbbell for 15 min at 160.degree. C. to measure the number of cycles required to cause fracture. The number of cycles required to cause fracture was measured for six dumbbells, i.e., n=6, and the probability of 50% survival was determined by normal probability distribution based on the number of cycles required to cause fracture, and the fatigue life was expressed in terms of an index by taking the probability of 50% survival in Comparative Example 4 as 100. The larger the numerical value, the longer the fatigue life.
(2) Strain-controlled fatigue life (after heat aging)
Heat aging was conducted in a gear oven at 80.degree. C. for 96 hr followed by measurement of the number of cycles required to cause fracture in the same manner as described above in connection with the strain-controlled fatigue life before heat aging.
Initial adhesion:
A plurality of brass-plated steel cords (cord structure: 1.times.5) were placed parallel to each other at intervals of 12.5 mm to form a long material both sides of which were then coated with the rubber composition to embed the long material in the rubber composition. The rubber composition with the long material embedded therein was brought to a fabric having a width of 25 mm which was then vulcanized for 20 min at 170.degree. C. to prepare a test sample. The steel cord was pulled out from the test sample in accordance with ASTM-D-2 to evaluate the coverage (%) of the coating rubber coating the surface of the pulled-out cord. The larger the numerical value, the better the initial adhesion.
Adhesion after immersion in warm water:
The test sample prepared for the evaluation of the initial adhesion was used as a sample for pulling out the cord by hand. The lower end cord of this sample was cut, followed by immersion and standing in warm water of 70.degree. C. for 4 weeks. Thereafter, the cord was pulled out to evaluate the degree of deterioration in adhesion caused by penetration of water due to an external damage in the same manner as described above in connection with the evaluation of the initial adhesion.
TABLE 4______________________________________ Comp. Ex. 4 Ex. 16 Ex. 17 Ex. 18______________________________________NR 100 100 100 100Carbon black 63 63 63 63L-Ascorbic acid 0.5 1.0 2.0Aromatic oil 4.0 4.0 4.0 4.0Zinc flower 10.0 10.0 10.0 10.0Cobalt naphthenate 3.0 3.0 3.0 3.0Antioxidant 1.0 1.0 1.0 1.0Sulfur 8.0 8.0 8.0 8.0Vulcanization accelerator 0.5 0.5 0.5 0.5Cresol resin 1.0 1.0 1.0 1.0Partial condensate ofhexamethylolmelamine 5.0 5.0 5.0 5.0pentamethyl etherFatigue resistanceStrain-controlled fatigue life 100 108 107 111(before heat aging)(Strain = 100%)Strain-controlled fatigue life 55 73 82 84(after heat aging)(Strain = 100%)Processability 28 27 25 22Scorching time (min)Breaking propertiesTensile strength 22.0 20.0 20.5 19.6@ Room temp./MPaElongation at break 380 370 380 390@ Room temp./%Initial adhesion 95 95 95 95Adhesion after immersion in 60 65 60 60warm water(hot water resistance)______________________________________ Note) NR: RSS #1 Carbon black: SEAST 300, manufactured by Tokai Carbon Co., Ltd. Aromatic oil: Process oil X140, manufactured by Kyodo Oil Co., Ltd. Zinc flower: Zinc flower R, manufactured by Toho Zinc Co., Ltd. Antioxidant: NPhenyl-N(1,3-dimethyl)-p-phenylenediamine (Antigene 6C, manufactured by Sumitomo Chemical Co. Ltd.) Sulfur: Insoluble sulfur (20% oiltreated) Vulcanization accelerator: N,NDicyclohexyl-2-dithiazolesulfenamide (Accel DZG, manufactured by Kawaguchi Chemical Industry Co., Ltd.) Cresol resin: SUMIKANOL 610, manufactured by Sumitomo Chemical Co., Ltd, Partial condensate of hexamethylolmelamine pentamethyl ether: SUMIKANOL 507 (content of partial condensate: 50%), manufactured by Sumitomo Chemical Co., Ltd.
As is apparent from Table 4, the rubber compositions of the present invention (Examples 16 to 18) were superior in fatigue resistance to the rubber composition not containing ascorbic acid (Comparative Example 4).
(5) Formulation ingredients (in parts by weight) specified in Table 5 were mixed and kneaded together by means of a Banbury mixer and a mixing roll according to a conventional method to prepare various rubber compositions (Examples 19 to 21 and Comparative Example 5). These rubber compositions were press-vulcanized at 160.degree. C. for 20 to 50 min, thereby preparing test pieces for a bead filler which were then evaluated for fatigue resistance, processability, and fracture properties in the same manner as described in the above item (4). The results are given in Table 5.
TABLE 5______________________________________ Comp. Ex. 5 Ex. 19 Ex. 20 Ex. 21______________________________________NR 80 80 80 80SBR 20 20 20 20Carbon black 70 70 70 70L-Ascorbic acid 0.5 1.0 2.0Aromatic oil 8.0 8.0 8.0 8.0Zinc flower 5.0 5.0 5.0 5.0Stearic acid 2.0 2.0 2.0 2.0Antioxidant 1.0 1.0 1.0 1.0Sulfur 3.5 35 3.5 35Vulcanization accelerator 1.0 1.0 1.0 1.0Fatigue resistanceStrain-controlled fatigue life 100 108 108 111(before heat aging)(Strain = 100%)Strain-controlled fatigue life 67 88 89 86(after heat aging)(Strain = 100%)Processability 22 20 18 15Scorching time (min)Breaking propertiesTensile strength 18.3 18.0 17.4 17.2@ Room temp./MPaElongation at break 260 250 240 280@ Room temp./%______________________________________ Note) NR: SIR20 BR: Nipol 1502, manufactured by Nippon Zeon Co. Ltd. Carbon black: SEAST N (N.sub.2 SA = 74 m.sup.2 /g), manufactured by Tokai Carbon Co., Ltd. Aromatic oil: Process oil X140, manufactured by Kyodo Oil Co., Ltd. Zinc flower: Zinc flower No. 3, manufactured by Seido Chemical Industry Co., Ltd. Stearic acid: Lunac YA, manufactured by Kao Corp. Antioxidant: NPhenyl-N(1,3-dimethyl)-p-phenylenediamine (Antigene 6C, manufactured by Sumitomo Chemical Co., Ltd.) Sulfur: Insoluble sulfur (20% oiltreated) Vulcanization accelerator: NTert-butyl-2-benzothiazolylsulfenamide (Nocceler NSF, manufactured by Ohuchi Shinko Chemical Industrial Co., Ltd.)
As is apparent from Table 5, the rubber compositions of the present invention (Examples 19 to 21) were superior in fatigue resistance to the rubber composition not containing ascorbic acid (Comparative Example 5).
(6) Then, using an ascorbic acid compound preparatively attached to silica or carbon black (these are each a filler for rubber), formulation ingredients (in parts by weight) specified in Table 6 were mixed and kneaded together by means of a Banbury mixer and a mixing roll according to a conventional method to prepare various rubber compositions (Examples 22 to 33 and Comparative Example). These rubber compositions were used to constitute treads of pneumatic tires for running on a general road which were then evaluated for abrasion resistance (Lambourn abrasion), processability (scorching time and dispersibility), and fracture properties (tensile strength and elongation at break) by the following methods. The results are given in Table 6.
Abrasion resistance:
Abrasion quantity was measured by a Lambourn abrasion test specified in JIS K6264 and expressed in terms of an index by taking the abrasion quantity in Comparative Example 6 as 100. The larger the numerical value, the better the abrasion resistance.
Processability:
The scorching time was evaluated by measuring the time taken for the torque to be increased by 5 points at 125.degree. C. in accordance with the procedure set forth in JIS K6300. The larger the numerical value, the better the processability.
The dispersibility was evaluated by cutting the vulcanized rubber with a sharp cutter, and the cut surface was inspected visually and under an optical microscope. "O" represents that no mass derived from poor dispersion was observed and homogeneous dispersion was attained; ".DELTA." represents that dispersion to some extent was attained although masses derived from poor dispersion were observed here and there; and "X" represents that a large number of masses derived from poor dispersion were observed.
Fracture properties:
The fracture properties were evaluated by measuring the tensile strength and the elongation at break. The larger the numerical value, the better the fracture properties (which means that fracture does not occur even upon larger deformation).
Method for measuring tensile strength:
The tensile strength was measured in accordance with the procedure set forth in JIS K6301 (tensile speed 500.+-.25 mm/min, testing temperature 23.degree..+-.2.degree. C., load cell capacity such that the tensile strength falls within 15 to 85% of the capacity, JIS No. 3, and n=3).
Method for measuring elongation at break:
As with the tensile strength, the elongation at break was measured in accordance with the procedure set forth in JIS K6301.
TABLE 6__________________________________________________________________________ Comp. Ex. 6 L- Ascorbic Ex. 22 Ex. 23 Ex. 24 Ex. 25 Ex. 26 Ex. 27 Ex. 28 Ex. 29 Ex. 30 Ex. 31 Ex. 32 Ex. acid not Coating carbon black Coating silica Directly introduced added__________________________________________________________________________SBR*.sup.1 100 100 100 100 100 100 100 100 100 100 100 100 100Carbon black (SAF) 40(45) 40(45) 40(45) 40(45) 45 45 45 45 45 45 45 45 45Silica 5 5 5 5 (5) (5) (5) (5) 5 5 5 5 5Surface-treated CB1*.sup.2 5.1Surface-treated CB2*.sup.2 5.3Surface-treated CB3*.sup.2 5.6Surface-treated CB4*.sup.2 6Surface-treated 6.1silica 1*.sup.3Surface-treated 6.3silica 2*.sup.3Surface-treated 6.6silica 3*.sup.3Surface-treated 7silica 4*.sup.3L-Ascorbic acid (0.1) (0.3) (0.6) (1) (0.1) (0.3) (0.6) (1) 0.1 0.3 0.6 1 0Dispersant*.sup.4 1 1 1 1 (1) (1) (1) (1) 1 1 1 1 1Aromatic oil 8 8 8 8 8 8 8 8 8 8 8 8 8Zinc flower 3 3 3 3 3 3 3 3 3 3 3 3 3Stearic acid 2 2 2 2 2 2 2 2 2 2 2 2 2Vulcanization 1.6 1.6 1.6 1.6 1.6 1.6 1.6 1.6 1.6 1.6 1.6 1.6 1.6accelerator*.sup.5Sulfur 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4Abrasion resistance 103 113 112 108 104 115 114 110 102 105 109 117 100Lambourn abrasionAbrasion index (%)ProcessabilityScorching time (min) 34.0 30.5 20.5 16.4 34.3 31.8 22.5 22.2 33.7 28.6 16.4 21.8 37.1Dispersibility .smallcircle. .smallcircle. .smallcircle. .smallcircle. .smallcircle. .smallcircle. .smallcircle. .smallcircle. .DELTA. x x x .smallcircle.Fracture propertiesTensile strength 22.1 24.1 23.0 21.8 23.0 22.6 22.8 22.2 22.5 22.3 23.5 21.8 23.1@ Room temp./MPaElongation at break 438 448 452 447 435 440 450 447 433 435 434 419 430@ Room temp./%__________________________________________________________________________Note)*Numerical value within the parentheses indicates a total value includingthe amount of L-ascorbic acid contained in the filler having a surfacetreatedwith L-ascorbic acid. The surface treatment of the filler (carbon blackor silica) with vitamin C was conducted by the following steps (a) to(d).(a) Prepare a solution of a necessary amount of L-ascorbic acid dissolvedin methanol in an amount of at least twice the weight of the filler tobesurface-treated.(b) In the case of silica, add 20% by weight, based on the silica, ofdiethylene glycol to the methanol solution.(c) Immerse the filler in this solution for 24 hr.(d) Dry at room temperature.*.sup.1 : SBR 1502*.sup.2 : Details of carbon blacks (CB) the surface of which was coatedwith L-ascorbic acid L-Ascorbic acid CBSurface-treated CB1 0.1 phr 5 phrSurface-treated CB2 0.3 phr 5 phrSurface-treated CB3 0.6 phr 5 phrSurface-treated CB4 1 phr 5 phr*.sup.3 : Details of silicas the surface of which was coated withL-ascorbic acid L-Ascorbic acid Silica Dispersant*4Surface-treated 0.1 phr 5 phr 1 phrsilica 1Surface-treated 0.3 phr 5 phr 1 phrsilica 2Surface-treated 0.6 phr 5 phr 1 phrsilica 3Surface-treated 1 phr 5 phr 1 phrsilica 4*4: Diethylene glycol (coated on the surface of silica for the purpose ofimproving the dispersibility of silica)*5: A mixture of N-cyclohexyl-2-benzothiazyl-sulfenamide withdiphenylguanidine
In Table 6, for Examples 22 to 25, carbon black (CB) having a surface coated with ascorbic acid was used; for Examples 26 to 29, silica having a surface coated with ascorbic acid was used; for Examples 30 to 33, carbon black, silica, and ascorbic acid were directly introduced in a separate manner; and for Comparative Example 6, ascorbic acid was not used.
As is apparent from Table 6, the rubber compositions of the present invention using carbon black or silica having a surface coated with ascorbic acid in an amount of 0.1 to 1 phr (part by weight based on 100 parts by weight of the rubber) (Examples 22 to 29) had better abrasion resistance than that of Comparative Example 6 and an improved dispersibility, and even although the use amount of the ascorbic acid was relatively limited, attained a higher effect of improvement relating to the abrasion resistance when compared with the compositions of Examples 30 to 33.
(7) Also, similar to the above, formulation ingredients (in parts by weight) specified in Table 7 were mixed and kneaded together by means of a Banbury mixer and a mixing roll according to a conventional method to prepare various rubber compositions (Examples 34 to 45 and Comparative Example 7). These rubber compositions were used to constitute treads of pneumatic tires for running on an expressway which were then evaluated for abrasion resistance (Lambourn abrasion), processability (scorching time and dispersibility), and fracture properties (tensile strength and elongation at break) in the same manner as described in the above item (6). The results are given in Table 7.
TABLE 7__________________________________________________________________________ Comp. Ex. 7 L- Ascorbic Ex. 34 Ex. 35 Ex. 36 Ex. 37 Ex. 38 Ex. 39 Ex. 40 Ex. 41 Ex. 42 Ex. 43 Ex. 44 Ex. acid not Coating carbon black Coating silica Directly introduced added__________________________________________________________________________Nipol 9502*.sup.1 137.5 137.5 137.5 137.5 137.5 137.5 137.5 137.5 137.5 137.5 137.5 137.5 137.5Carbon black (SAF) 60(80) 60(80) 60(80) 60(80) 80 80 80 80 80 80 80 80 80Silica 20 20 20 20 (20) (20) (20) (20) 20 20 20 20 20Surface-treated CB1*.sup.2 20.1Surface-treated CB2*.sup.2 22Surface-treated CB3*.sup.2 24Surface-treated CB4*.sup.2 26Surface-treated 21.1silica 1*.sup.3Surface-treated 23silica 2*.sup.3Surface-treated 25silica 3*.sup.3Surface-treated 27silica 4*.sup.3L-Ascorbic acid (0.1) (2) (4) (5) (0.1) (2) (4) (5) 0.1 2 4 5 0Dispersant*.sup.4 1 1 1 1 (1) (1) (1) (1) 1 1 1 1 1Aromatic oil 25 25 25 25 25 25 25 25 25 25 25 25 25Zinc flower 3 3 3 3 3 3 3 3 3 3 3 3 3Stearic acid 2 2 2 2 2 2 2 2 2 2 2 2 2Vulcanization 1.6 1.6 1.6 1.6 1.6 1.6 1.6 1.6 1.6 1.6 1.6 1.6 1.6accelerator*.sup.5Sulfur 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4 2.4Abrasion resistance 104 113 112 105 103 111 114 107 102 107 112 110 100Lambourn abrasionAbrasion index (%)ProcessabilityScorching time (min) 25.0 22.1 20.4 15.7 25.3 21.7 20.1 20.1 25.0 13.2 8.3 7.5 26.2Dispersibility .smallcircle. .smallcircle. .smallcircle. .smallcircle. .smallcircle. .smallcircle. .smallcircle. .smallcircle. .DELTA. x x x .smallcircle.Fracture propertiesTensile strength 20.1 20.0 20.4 21.0 21.0 20.1 20.4 21.9 20.9 21.6 20.2 21.3 20.8@ Room temp./MPaElongation at break 472 594 570 579 483 560 569 580 470 557 510 508 461@ Room temp./%__________________________________________________________________________Note)*Numerical value within the parentheses indicates a total value includingthe amount of L-ascorbic acid contained in the filler having a surfacetreated with L-ascorbic acid. The surface treatment of the filler (carbonblack or silica) with L-ascorbic acid was conducted by the followingsteps (a) to (d).(a) Prepare a solution of a necessary amount of L-ascorbic acid dissolvedin methanol in an amount of twice the weight of the filler to besurface-treated.(b) In the case of silica, add 5% by weight, based on the silica, ofdiethylene glycol to the methanol solution.(c) Immerse the filler in this solution for 24 hr.(d) Dry at room temperature.*.sup.1 : Oil extended SBR (amount of oil: 37.5 phr)*.sup.2 : Details of carbon blacks (CB) the surface of which was coatedwith L-ascorbic acid L-Ascorbic acid CBSurface-treated CB1 0.1 phr 20 phrSurface-treated CB2 2 phr 20 phrSurface-treated CB3 4 phr 20 phrSurface-treated CB4 5 phr 20 phr*.sup.3 : Details of silicas the surface of which was coated withL-ascorbic acid L-Ascorbic acid Silica Dispersant*4Surface-treated 0.1 phr 20 phr 1 phrsilica 1Surface-treated 2 phr 20 phr 1 phrsilica 2Surface-treated 4 phr 20 phr 1 phrsilica 3Surface-treated 5 phr 20 phr 1 phrsilica 4*4: Diethylene glycol (coated on the surface of silica for the purpose ofimproving the dispersibility of silica)*5: A mixture of N-cyclohexyl-2-benzothiazyl-sulfenamide withdiphenylguanidine
In Table 7, for Examples 34 to 37, carbon black (CB) having a surface coated with ascorbic acid was used; for Examples 38 to 41, silica having a surface coated with ascorbic acid was used; for Examples 42 to 45, carbon black, silica and ascorbic acid were directly introduced in a separate manner; and for Comparative Example 7, ascorbic acid was not used.
As is apparent from Table 7, the rubber compositions of the present invention using carbon black or silica having a surface coated with ascorbic acid in an amount of 0.1 to 5 phr (Examples 34 to 39) had a better abrasion resistance than that of Comparative Example 7, were improved in or relating to the dispersibity and the scorch prevention and not degraded with respect to the fracture properties when compared with the compositions of Examples 42 to 45.
As described above, according to the present invention, by virtue of the incorporation of at least one compound selected from the group consisting of ascorbic acid and derivatives thereof, tocopherols, and citric acid and derivatives thereof, it is possible to provide a rubber composition for a tire which can improve the abrasion resistance without sacrificing wet performance, fracture properties, and heat build-up and, at the same time, has enhanced crack resistance and fatigue resistance and, hence, can improve tire durability.

Number	Date	Country
8-046390	Mar 1996	JPX
8-321887	Dec 1996	JPX
9-014077	Jan 1997	JPX

Number	Name	Date
3929804	Cook	Dec 1975
4143423	Sternlieb	Mar 1979
4304707	Kuehn	Dec 1981
4859744	Lindner	Aug 1989
5073366	Moltrasio	Dec 1991
5270060	Foster	Dec 1993
5384349	Trepka	Jan 1995
5457216	Kleinknecht	Oct 1995
5525646	Lundgren	Jun 1996
5629363	Abber	May 1997

Rubber composition for tire

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