CN109384964B - Rubber composition for tire side wall of tire, vulcanized rubber, and preparation method and application thereof - Google Patents
Rubber composition for tire side wall of tire, vulcanized rubber, and preparation method and application thereof Download PDFInfo
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Abstract
The invention relates to the field of rubber, and discloses a rubber composition and vulcanized rubber for a tire side wall of a tire, and a preparation method and application thereof. The rubber composition has the advantages of high strength, low rolling resistance and good dynamic bending flexibility, and the vulcanized rubber formed by the composition can be used for the tire side wall.
Description
Technical Field
The invention relates to the field of rubber, in particular to a rubber composition for a tire side wall, a method for preparing vulcanized rubber, the vulcanized rubber prepared by the method and application of the vulcanized rubber in the tire side wall.
Background
In recent years, in order to adapt to the development trend of safety, environmental protection and green of automobile tires, non-petroleum resources such as white carbon black are more and more emphasized in the field of tires due to the characteristics of reducing the rolling resistance of tires, saving the fuel consumption of automobiles and the like, but the dispersion of white carbon black in a rubber matrix becomes extremely difficult due to the strong surface polarity of white carbon black, so that the application of white carbon black is limited to a certain extent.
CN104530501A discloses a rubber composition for color tire sidewall discoloration resistance, which has bright colors and better discoloration resistance, wherein a dark color sidewall tire does not have discoloration phenomenon within one year under the environment of strong illumination and damp heat, and the formula has higher tearing resistance and excellent discoloration resistance under the severe use conditions of strong illumination and damp heat. CN104311918A discloses a rubber composition for the sidewall of a run-flat tire for a passenger car, which can improve the safety performance of the vehicle during running and reduce or eliminate traffic accidents caused by puncture and explosion of the tire.
However, in the above prior art, it is disclosed that the silica white is added with silane coupling agent Si75, etc. to improve the dispersibility, while Si75, etc. is a sulfur-containing compound, and during the high-temperature mixing process, the requirement for process control is high, and improper control thereof may cause scorching, which may further affect the overall performance of the composite material. Si75 and the like are easy to generate ethanol in the processing process, and the existence of the ethanol brings hidden danger to the safety of the tire.
Therefore, the above prior art cannot fully satisfy the requirements of high strength, low rolling resistance, and good dynamic bending flexibility required for the tire sidewall rubber containing the white carbon black formulation, and there is a need for providing a rubber composition with improved properties.
Disclosure of Invention
The invention aims to solve the problems of improving the strength, reducing the rolling resistance and dynamic bending flexibility of rubber used for a tire side wall containing white carbon black formula, and provides a rubber composition with the advantages of high strength, low rolling resistance and good dynamic bending flexibility and vulcanized rubber formed by the composition and capable of being used for the tire side wall.
In order to achieve the above object, the present invention provides a rubber composition for a sidewall of a tire, the composition comprising a rubber matrix, a rubber modifier, white carbon black, an activator, an antioxidant, a softener, an accelerator and a vulcanizing agent, wherein the rubber modifier is a maleic acid-based monomer, and the rubber matrix is a mixture of butadiene rubber and natural rubber.
In a second aspect, the present invention provides a process for preparing a vulcanizate, the process comprising:
(1) carrying out first mixing on a component A containing a rubber matrix and a rubber modifier to obtain a section of master batch;
(2) carrying out second mixing on the first-stage masterbatch and a component B containing white carbon black, an activating agent, an anti-aging agent and a softening agent to obtain a second-stage masterbatch;
(3) performing third mixing on the second-stage masterbatch and a component C containing an accelerator and a vulcanizing agent to obtain a final rubber compound;
(4) vulcanizing the final rubber;
the rubber modifier is maleic acid monomer, and the rubber matrix is a mixture of butadiene rubber and natural rubber.
The vulcanized rubber is obtained by a novel mixing method, wherein a rubber matrix and a rubber modifier are mixed to prepare a matrix master batch; then adding the white carbon black, the activator, the anti-aging agent, the softener and other components into the matrix masterbatch to mix to prepare second-stage masterbatch; and then adding a vulcanizing agent and an accelerator into the secondary masterbatch to prepare final rubber, and finally vulcanizing the final rubber to prepare the vulcanized rubber. In the processing technology, the bridge function of the rubber modifier in the rubber matrix and the white carbon black can be better exerted, the dispersion of the white carbon black in the rubber matrix is facilitated, the strength of vulcanized rubber prepared by further vulcanization can be better improved, the rolling resistance of the vulcanized rubber is reduced, and the bending resistance and flexibility of the vulcanized rubber material are improved.
In a third aspect, the present invention provides a vulcanizate prepared by the method of the second aspect described above.
In a fourth aspect, the present invention provides the use of the vulcanizate of the third aspect described above in a tire sidewall.
The rubber composition has the advantages of high strength, low rolling resistance and good dynamic bending flexibility, and the vulcanized rubber formed by the composition can be used for the tire side wall.
Detailed Description
The endpoints of the ranges and any values disclosed herein are not limited to the precise range or value, and such ranges or values should be understood to encompass values close to those ranges or values. For ranges of values, between the endpoints of each of the ranges and the individual points, and between the individual points may be combined with each other to give one or more new ranges of values, and these ranges of values should be considered as specifically disclosed herein.
As described above, the first aspect of the present invention provides a rubber composition for a sidewall of a tire, which contains a rubber matrix, a rubber modifier, white carbon black, an activator, an anti-aging agent, a softener, an accelerator and a vulcanizing agent, wherein the rubber modifier is a maleic acid-based monomer, and the rubber matrix is a mixture of butadiene rubber and natural rubber.
The maleic acid monomer can modify a rubber matrix, is beneficial to interaction between the rubber matrix and white carbon black, is beneficial to dispersion of the white carbon black in the rubber matrix, can better improve the strength of vulcanized rubber prepared by further vulcanization, reduces the rolling resistance of the vulcanized rubber, and improves the bending resistance and flexibility of a vulcanized rubber material.
Preferably, the maleic acid-based monomer is at least one selected from the group consisting of maleic acid, maleic anhydride and dialkyl maleate.
Preferably, the natural rubber is contained in the rubber matrix in an amount of 40 to 60 parts by weight and the butadiene rubber is contained in an amount of 40 to 60 parts by weight, relative to 100 parts by weight of the rubber matrix.
Preferably, the natural rubber is SMR-20.
Preferably, the cis content in the butadiene rubber is 90 to 99 wt%.
Preferably, the rubber modifier is 5 to 12 parts by weight, the white carbon black is 20 to 50 parts by weight, the carbon black is 30 to 50 parts by weight, the activator is 5 to 10 parts by weight, the antioxidant is 1 to 3 parts by weight, the softener is 5 to 15 parts by weight, the accelerator is 1 to 5 parts by weight, and the vulcanizing agent is 0.5 to 4 parts by weight, based on 100 parts by weight of the rubber matrix.
According to the present invention, preferably, the white carbon black is silica; more preferably, the nitrogen adsorption specific surface area of the white carbon black is 10-200m2(ii) in terms of/g. For example, the white carbon black is 115GR (Rodiya, France) and/or 165GR (Rodiya, France).
Preferably, the carbon black has a CTAB adsorption specific surface area of 10 to 600m2(ii) in terms of/g. For example, the carbon black is N330 (Zideli chemical technologies, Inc. of Dongguan) and/or N550 (Zideli chemical technologies, Inc. of Dongguan).
Preferably, the activator is a mixture of a metal oxide and a fatty acid or a fatty acid metal soap salt. The metal oxide is preferably zinc oxide and/or magnesium oxide; the fatty acid is preferably stearic acid; the fatty acid metal soap salt is zinc stearate and/or zinc borate.
Preferably, the antioxidant is at least one of an amine antioxidant, a quinoline antioxidant and a benzimidazole antioxidant. For example, the antioxidant is antioxidant 4020.
Preferably, the softening agent is at least one of aromatic oil, paraffin oil, naphthenic oil, petroleum resin, and polyethylene glycol. The aromatic oil may be, for example, aromatic oil TDAE V500.
Preferably, the accelerator is at least one of a sulfenamide accelerator, a thiazole accelerator, a thiuram accelerator and a guanidine accelerator. Preferably, the accelerator is N-tert-butyl-2-benzothiazolesulfenamide (TBBS) and/or diphenylguanidine (accelerator D).
Preferably, the vulcanizing agent is a sulfur donor. The sulfur donor is a substance capable of providing sulfur. The sulfur comprises at least one of insoluble sulfur, soluble sulfur and oil-extended sulfur. For example, the vulcanizing agent IS ordinary sulfur S, oil-extended insoluble sulfur IS, or the like.
As previously mentioned, a second aspect of the present invention provides a process for preparing a vulcanized rubber, the process comprising:
(1) carrying out first mixing on a component A containing a rubber matrix and a rubber modifier to obtain a section of master batch;
(2) carrying out second mixing on the first-stage masterbatch and a component B containing white carbon black, an activating agent, an anti-aging agent and a softening agent to obtain a second-stage masterbatch;
(3) performing third mixing on the second-stage masterbatch and a component C containing an accelerator and a vulcanizing agent to obtain a final rubber compound;
(4) vulcanizing the final rubber;
the rubber modifier is maleic acid monomer, and the rubber matrix is a mixture of butadiene rubber and natural rubber.
The component a, the component B and the component C referred to in the second aspect of the present invention together form the rubber composition for a tire side wall described in the first aspect of the present invention, and therefore, each of the substances referred to in the second aspect of the present invention has the corresponding same properties as the same substances in the first aspect of the present invention, and in order to avoid repetition, the present invention does not repeat certain features of the substances (such as optional kinds of substances, etc.) in the second aspect, and those skilled in the art should not be construed as limiting the second aspect of the present invention.
The component A containing the rubber matrix and the rubber modifier is firstly mixed to obtain a section of masterbatch, and then the subsequent process steps are carried out, so that the obtained vulcanized rubber has more excellent properties such as strength, rolling resistance and the like.
Preferably, in the second aspect, the maleic acid-based monomer is selected from at least one of maleic acid, maleic anhydride, and dialkyl maleate.
Preferably, in the second aspect, the natural rubber is used in an amount of 40 to 60 parts by weight and the butadiene rubber is used in an amount of 40 to 60 parts by weight, relative to 100 parts by weight of the rubber matrix.
Preferably, in the second aspect, the natural rubber is SMR-20.
Preferably, in the second aspect, the cis content in the cis-butadiene rubber is 90 to 99% by weight.
Preferably, in the second aspect, the rubber modifier is used in an amount of 5 to 12 parts by weight, the white carbon black is used in an amount of 20 to 50 parts by weight, the carbon black is used in an amount of 30 to 50 parts by weight, the activator is used in an amount of 5 to 10 parts by weight, the antioxidant is used in an amount of 1 to 3 parts by weight, the softener is used in an amount of 5 to 15 parts by weight, the accelerator is used in an amount of 1 to 5 parts by weight, and the vulcanizing agent is used in an amount of 0.5 to 4 parts by weight, relative to 100 parts by weight of the rubber base.
Preferably, in the second aspect, the conditions for the first mixing include: the temperature is 130-170 ℃ and the time is 3-10 min. More preferably, the conditions of the first mixing include: the temperature is 140 ℃ and 150 ℃, and the time is 5-8 min.
Preferably, in the second aspect, the conditions for the second mixing include: the temperature is 100 ℃ and 150 ℃, and the time is 3-10 min. More preferably, the conditions of the second mixing include: the temperature is 110-120 ℃, and the time is 5-7 min.
Preferably, in the second aspect, the third mixing conditions include: the temperature is not more than 130 deg.C, and the time is 5-7 min.
Preferably, in the second aspect, the vulcanization conditions include: the temperature is 150 ℃ and 170 ℃, the pressure is 10-20MPa, and the time is 30-50 min.
In a second aspect of the present invention, according to a preferred embodiment, the conditions of the first mixing include: the temperature is 140 ℃ and 150 ℃, and the time is 5-8 min; the conditions of the second mixing include: the temperature is 110-120 ℃, and the time is 5-7 min; the conditions of the third mixing include: the temperature is not more than 130 ℃, and the time is 5-7 min; and the conditions of the vulcanization include: the temperature is 150 ℃ and 170 ℃, the pressure is 10-20MPa, and the time is 30-50 min. The vulcanized rubber prepared by the preferred embodiment has better mechanical properties (improved strength and reduced heat generation), and the vulcanized rubber has longer service life (excellent heat generation reduction).
To specifically illustrate the process of the present invention for preparing a vulcanizate, a preferred embodiment is provided below for illustration:
(1) placing the rubber matrix in an internal mixer, plasticating at the rotation speed of 50-120 rpm, the initial mixing temperature of 70-90 ℃ and the raw rubber plasticating time of 0.1-1 min; then introducing the component A containing the rubber modifier into the internal mixer for first mixing to obtain a section of master batch;
(2) adding the first-stage masterbatch and a component B containing white carbon black, an activating agent, an anti-aging agent and a softening agent into an internal mixer for second mixing, discharging and standing for 3-5 hours to obtain second-stage masterbatch;
(3) setting the rotation speed of an internal mixer to be 50-100 rpm, setting the initial mixing temperature to be 25-50 ℃, plasticating the two-stage masterbatch for 0.5-1.5 min, and adding a component C containing an accelerator and a vulcanizing agent to carry out third mixing to obtain final rubber;
(4) putting the final rubber compound into a vulcanizing press for vulcanization;
the rubber modifier is maleic acid monomer, and the rubber matrix is a mixture of butadiene rubber and natural rubber.
The pressures used in the present invention are gage pressures.
As previously mentioned, a third aspect of the present invention provides a vulcanizate prepared by the method of the second aspect described above.
As previously mentioned, a fourth aspect of the present invention provides the use of the vulcanizate of the third aspect described above in a sidewall for a tire.
The present invention will be described in detail below by way of examples.
Unless otherwise specified, various commercial products used below are commercially available.
The following examples and comparative examples the equipment for the preparation of vulcanizates are shown in Table 1.
The apparatus for testing the vulcanized rubbers obtained in the examples and comparative examples is shown in Table 2, and the test conditions are shown in Table 3.
The chemicals used in the examples and comparative examples are commercially available and are specified below:
natural rubber: SMR-20, Qingdao Seritet International Logistics, Inc.;
butadiene rubber: BR9000, a yanshan petrochemical (wherein, the cis content is 97.8 mass%);
white carbon black: 165GR, Rodiya, France, nitrogen adsorption specific surface area 170m2/g；
Carbon black: n330, CTAB adsorption specific surface area of 75m2Per kg; n550, CTAB adsorption specific surface area of 103m2Kg, Zideli chemical technology Co., Ltd, Dongguan;
rubber modifier: maleic anhydride (Jessie Ka chemical Co., Ltd., Hangzhou), diethyl maleate (Jinnan Zi Anhua chemical Co., Ltd.), maleic acid (Bailingwei science and technology Co., Ltd.), diisopropyl maleate (Shaanxi Baoyu Jade chemical Co., Ltd.);
softening agent: environmental aromatic oil TDAE V500 (TDAE for short), xindayang (ningbo) limited;
activating agent: zinc oxide, stearic acid, Weifang Heng Feng chemical Limited;
an anti-aging agent: n- (1, 3-dimethylbutyl) -N' -phenyl-p-phenylenediamine (antioxidant 4020) Jiangsu san ao chemical technology, Inc.;
vulcanizing agent: sulfur, Heicheng Hechenghuai chemical Limited;
accelerator (b): n-tert-butyl-2-benzothiazolesulfenamide (TBBS), diphenylguanidine (accelerator D), tetramethylthiuram disulfide (TMTD), Shanghai Yongyan chemical science and technology Co., Ltd.
The components in the following examples and comparative examples were used in parts by weight, each representing 1 g.
The examples are intended to illustrate the rubber compositions, vulcanizates, and methods of making the same of the present invention.
TABLE 1
| Serial number | Device name | Model number | Manufacturer of the product |
| 1 | Internal mixer | BR1600 | Farrel America Ltd |
| 2 | Flat vulcanizing machine | XLB-D400*400*2 | Shanghai first rubber machinery plant |
TABLE 2
TABLE 3
Example 1
The rubber composition formula comprises: 60 parts of natural rubber, 40 parts of butadiene rubber, 5 parts of maleic anhydride (rubber modifier), 20 parts of white carbon black, 20 parts of carbon black N55020 parts of carbon black N33030 parts of carbon black, 15 parts of TDAE (softening agent), 4 parts of zinc oxide (activating agent), 1 part of stearic acid (activating agent), 0.5 part of sulfur (vulcanizing agent), 5 parts of TBBS (accelerator) and 1 part of anti-aging agent 4020 (anti-aging agent).
The preparation process of the vulcanized rubber comprises the following steps:
(1) carrying out first mixing on a rubber matrix and a rubber modifier to obtain a section of master batch; concretely, adding natural rubber and butadiene rubber into an internal mixer, setting the rotating speed to be 80rpm, setting the initial mixing temperature to be 80 ℃, and setting the raw rubber plasticating time to be 0.5 min; adding a rubber modifier into the internal mixer for mixing at the mixing temperature of 140 ℃ for 8min to obtain a section of master batch;
(2) carrying out second mixing on the first-stage masterbatch, the white carbon black, the activating agent, the anti-aging agent, the softening agent and the carbon black to obtain second-stage masterbatch; specifically, adding white carbon black, TDAE, zinc oxide, stearic acid and an anti-aging agent 4020 into an internal mixer, carrying out second mixing with the first-stage masterbatch, wherein the mixing time is 7min, the rubber discharge temperature is 110 ℃, discharging and standing for 4 hours to obtain a second-stage masterbatch;
(3) carrying out third mixing on the second-stage masterbatch, an accelerant and a vulcanizing agent to obtain final rubber; specifically, setting the rotation speed of an internal mixer to be 80rpm, setting the initial mixing temperature to be 40 ℃, plasticating the two-stage masterbatch for 1min, adding a vulcanizing agent and an accelerator to perform third mixing, setting the mixing temperature to be 105 ℃, mixing for 7min, and discharging to obtain final mixed rubber;
(4) and (3) putting the final rubber compound into a flat vulcanizing machine for vulcanization, wherein the vulcanization temperature is 150 ℃, the vulcanization pressure is 20MPa, and the vulcanization time is 50min, so that a vulcanized rubber sample S1 is obtained.
The cured rubber sample S1 was subjected to the performance test, and the results are shown in Table 4.
Example 2
The rubber composition formula comprises: 40 parts of natural rubber, 60 parts of butadiene rubber, 12 parts of diethyl maleate (rubber modifier), 50 parts of white carbon black, N55030 parts of carbon black, 5 parts of TDAE (softening agent), 4 parts of zinc oxide (activating agent), 3 parts of stearic acid (activating agent), 4 parts of sulfur (vulcanizing agent), 1 part of TMTD (accelerator) and 2 parts of anti-aging agent 4020 (anti-aging agent).
The preparation process of the vulcanized rubber comprises the following steps:
(1) carrying out first mixing on a rubber matrix and a rubber modifier to obtain a section of master batch; concretely, adding natural rubber and butadiene rubber into an internal mixer, setting the rotating speed to be 80rpm, setting the initial mixing temperature to be 80 ℃, and setting the raw rubber plasticating time to be 0.5 min; adding a rubber modifier into the internal mixer for mixing at 145 ℃ for 6min to obtain a section of master batch;
(2) carrying out second mixing on the first-stage masterbatch, the white carbon black, the activating agent, the anti-aging agent, the softening agent and the carbon black to obtain second-stage masterbatch; specifically, adding white carbon black, TDAE, zinc oxide, stearic acid and an anti-aging agent 4020 into an internal mixer, carrying out second mixing with the first-stage masterbatch, wherein the mixing time is 6min, the rubber discharge temperature is 115 ℃, discharging and standing for 5 hours to obtain a second-stage masterbatch;
(3) carrying out third mixing on the second-stage masterbatch, an accelerant and a vulcanizing agent to obtain final rubber; specifically, setting the rotation speed of an internal mixer to be 80rpm, setting the initial mixing temperature to be 40 ℃, plasticating the two-stage masterbatch for 1min, adding a vulcanizing agent and an accelerator to perform third mixing, setting the mixing temperature to be 110 ℃, mixing for 6min, and discharging to obtain final mixed rubber;
(4) and (3) putting the final rubber compound into a flat vulcanizing machine for vulcanization, wherein the vulcanization temperature is 170 ℃, the vulcanization pressure is 10MPa, and the vulcanization time is 30min, so that a vulcanized rubber sample S2 is obtained.
The cured rubber sample S2 was subjected to the performance test, and the results are shown in Table 4.
Example 3
The rubber composition formula comprises: 50 parts of natural rubber, 50 parts of butadiene rubber, 8 parts of maleic acid (rubber modifier), 35 parts of white carbon black, 40 parts of carbon black N330, 10 parts of TDAE (softening agent), 3 parts of zinc oxide (activating agent), 7 parts of stearic acid (activating agent), 2 parts of sulfur (vulcanizing agent), 1 part of TBBS (accelerating agent), 2 parts of accelerating agent D (accelerating agent) and 3 parts of anti-aging agent 4020 (anti-aging agent).
The preparation process of the vulcanized rubber comprises the following steps:
(1) carrying out first mixing on a rubber matrix and a rubber modifier to obtain a section of master batch; concretely, adding natural rubber and butadiene rubber into an internal mixer, setting the rotating speed to be 80rpm, setting the initial mixing temperature to be 80 ℃, and setting the raw rubber plasticating time to be 0.5 min; adding a rubber modifier into the internal mixer for mixing at the mixing temperature of 150 ℃ for 5min to obtain a section of master batch;
(2) carrying out second mixing on the first-stage masterbatch, the white carbon black, the activating agent, the anti-aging agent, the softening agent and the carbon black to obtain second-stage masterbatch; specifically, adding white carbon black, TDAE, zinc oxide, stearic acid and an anti-aging agent 4020 into an internal mixer, carrying out second mixing with the first-stage masterbatch, wherein the mixing time is 5min, the rubber discharge temperature is 120 ℃, discharging and standing for 4 hours to obtain a second-stage masterbatch;
(3) carrying out third mixing on the second-stage masterbatch, an accelerant and a vulcanizing agent to obtain final rubber; specifically, setting the rotation speed of an internal mixer to be 80rpm, setting the initial mixing temperature to be 40 ℃, plasticating the two-stage master batch for 1min, adding a vulcanizing agent and an accelerator to perform third mixing, setting the mixing temperature to be 120 ℃, mixing for 5min, and discharging to obtain final mixed rubber;
(4) and (3) putting the final rubber compound into a flat vulcanizing machine for vulcanization, wherein the vulcanization temperature is 160 ℃, the vulcanization pressure is 15MPa, and the vulcanization time is 40min, so that a vulcanized rubber sample S3 is prepared.
The cured rubber sample S3 was subjected to the performance test, and the results are shown in Table 4.
Example 4
The rubber composition formula comprises: 50 parts of natural rubber, 50 parts of butadiene rubber, 8 parts of diisopropyl maleate (rubber modifier), 35 parts of white carbon black, 40 parts of carbon black N33040, 10 parts of TDAE (softening agent), 3 parts of zinc oxide (activating agent), 7 parts of stearic acid (activating agent), 2 parts of sulfur (vulcanizing agent), 1 part of TBBS (accelerating agent), 2 parts of accelerating agent D (accelerating agent) and 3 parts of anti-aging agent 4020 (anti-aging agent).
The procedure for the preparation of the vulcanizates was the same as in example 3. A vulcanized rubber sample S4 was obtained.
The cured rubber sample S4 was subjected to the performance test, and the results are shown in Table 4.
Example 5
The rubber composition formulation of this example was the same as in example 3, and a vulcanized rubber was prepared in a similar manner to example 3, except that:
the procedure for the preparation of the vulcanizates was similar to that in example 3, except that:
in the process of preparing the first-stage masterbatch, the temperature of first mixing is 130 ℃, and the time is 4 min;
in the process of preparing the second-stage masterbatch, the temperature of second mixing is 130 ℃, and the time is 6 min;
in the process of preparing the final rubber compound, the time of the third mixing is 6min, and the rubber discharging temperature is 130 ℃.
A vulcanized rubber sample S5 was obtained.
The cured rubber sample S5 was subjected to the performance test, and the results are shown in Table 4.
Comparative example 1
The rubber composition formula comprises: 50 parts of natural rubber, 50 parts of butadiene rubber, 698 parts of Si, 35 parts of white carbon black, 33040 parts of carbon black N, 10 parts of TDAE (softening agent), 3 parts of zinc oxide (activating agent), 7 parts of stearic acid (activating agent), 2 parts of sulfur (vulcanizing agent), 1 part of TBBS (accelerating agent), 2 parts of accelerating agent D (accelerating agent) and 3 parts of anti-aging agent 4020 (anti-aging agent).
The procedure for the preparation of the vulcanizates was the same as in example 3. A vulcanizate sample DS1 was prepared.
The cured rubber sample DS1 was subjected to performance testing and the results are shown in Table 4.
TABLE 4
| Sample numbering | S1 | S2 | S3 | S4 | S5 | DS1 |
| Tear Strength (MPa) | 19.3 | 19.2 | 19.5 | 18.9 | 18.0 | 16.8 |
| Compression temperature rise (. degree.C.) | 28.3 | 28.6 | 28.3 | 28.8 | 30.0 | 32.0 |
| Fatigue life (times) | 18203 | 17900 | 17994 | 17850 | 16002 | 15478 |
As can be seen from the results in Table 4, the rubber composition of the present invention can achieve better dispersibility of the components of the rubber composition in the rubber matrix, so that the further prepared vulcanized rubber can have excellent comprehensive properties such as improved strength, reduced heat generation, improved dynamic fatigue property, etc.
The preferred embodiments of the present invention have been described above in detail, but the present invention is not limited thereto. Within the scope of the technical idea of the invention, many simple modifications can be made to the technical solution of the invention, including combinations of various technical features in any other suitable way, and these simple modifications and combinations should also be regarded as the disclosure of the invention, and all fall within the scope of the invention.
Claims (15)
1. A rubber composition for a tire side wall of a vehicle comprises a rubber matrix, a rubber modifier, white carbon black, an activator, an anti-aging agent, a softener, an accelerator and a vulcanizing agent, wherein the rubber modifier is a maleic acid monomer, the rubber matrix is a mixture of butadiene rubber and natural rubber, and the maleic acid monomer is at least one selected from maleic acid, maleic anhydride and dialkyl maleate;
the content of the natural rubber in the rubber matrix is 40-60 parts by weight and the content of the butadiene rubber is 40-60 parts by weight relative to 100 parts by weight of the rubber matrix; wherein the natural rubber is SMR-20; the cis content in the butadiene rubber is 90-99 wt%;
relative to 100 parts by weight of the rubber matrix, the rubber modifier is 5-12 parts by weight, the white carbon black is 20-50 parts by weight, the carbon black is 30-50 parts by weight, the activator is 5-10 parts by weight, the anti-aging agent is 1-3 parts by weight, the softener is 5-15 parts by weight, the accelerator is 1-5 parts by weight, and the vulcanizing agent is 0.5-4 parts by weight.
2. The composition according to claim 1, wherein the silica has a nitrogen adsorption specific surface area of 10 to 200m2/g。
3. The composition according to claim 1 or 2, wherein the carbon black has a CTAB adsorption specific surface area of 10 to 600m2/g。
4. A composition according to claim 1 or 2, wherein the activator is a mixture of a metal oxide and a fatty acid or a fatty acid metal soap salt.
5. The composition according to claim 1 or 2, wherein the antioxidant is at least one of an amine antioxidant, a quinoline antioxidant, and a benzimidazole antioxidant.
6. The composition according to claim 1 or 2, wherein the softening agent is at least one of aromatic oil, paraffin oil, naphthenic oil, petroleum resin, and polyethylene glycol.
7. The composition of claim 1 or 2, wherein the accelerator is at least one of a sulfenamide accelerator, a thiazole accelerator, a thiuram accelerator, and a guanidine accelerator.
8. The composition according to claim 1 or 2, wherein the vulcanizing agent is a sulfur donor.
9. A method of preparing a vulcanized rubber, the method comprising:
(1) carrying out first mixing on a component A containing a rubber matrix and a rubber modifier to obtain a section of master batch;
(2) carrying out second mixing on the first-stage masterbatch and a component B containing white carbon black, an activating agent, an anti-aging agent and a softening agent to obtain a second-stage masterbatch;
(3) performing third mixing on the second-stage masterbatch and a component C containing an accelerator and a vulcanizing agent to obtain a final rubber compound;
(4) vulcanizing the final rubber;
the rubber modifier is maleic acid monomer, the rubber matrix is a mixture of butadiene rubber and natural rubber, and the maleic acid monomer is at least one selected from maleic acid, maleic anhydride and maleic acid dialkyl ester;
the content of the natural rubber in the rubber matrix is 40-60 parts by weight and the content of the butadiene rubber is 40-60 parts by weight relative to 100 parts by weight of the rubber matrix; wherein the natural rubber is SMR-20; the cis content in the butadiene rubber is 90-99 wt%;
relative to 100 parts by weight of the rubber matrix, the rubber modifier is 0.5-4 parts by weight, the white carbon black is 20-50 parts by weight, the carbon black is 30-50 parts by weight, the activator is 5-10 parts by weight, the anti-aging agent is 1-3 parts by weight, the softener is 5-15 parts by weight, the accelerator is 1-5 parts by weight, and the vulcanizing agent is 0.5-4 parts by weight.
10. The method of claim 9, wherein the conditions of the first mixing comprise: the temperature is 130-170 ℃ and the time is 3-10 min.
11. The method of claim 9, wherein the conditions of the second mixing comprise: the temperature is 100 ℃ and 150 ℃, and the time is 3-10 min.
12. The method of claim 9, wherein the conditions of the third mixing comprise: the temperature is not more than 130 deg.C, and the time is 5-7 min.
13. The method of claim 9, wherein the conditions of the sulfiding comprise: the temperature is 150 ℃ and 170 ℃, the pressure is 10-20MPa, and the time is 30-50 min.
14. A vulcanized rubber produced by the process of any one of claims 9 to 13.
15. Use of the vulcanizate of claim 14 in a tire sidewall.
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| CN114149624B (en) * | 2020-09-07 | 2023-08-15 | 中国石油化工股份有限公司 | Rubber composition for light tire sidewall and application thereof, vulcanized rubber and preparation method and application thereof |
| CN115716940B (en) * | 2021-08-24 | 2024-05-07 | 中国石油化工股份有限公司 | Rubber composition, vulcanized rubber, preparation method and application thereof |
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