• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The present invention relates to a resin composition for rubber compounding and a rubber composition containing the same, and more particularly, a phenol resin, an epoxy resin having at least two or more epoxy groups in one molecule, and a butadiene-acrylonitrile polymer having a functional group in a sock end. It relates to a rubber composition and a rubber composition containing the same, characterized in that it is included. The resin composition for rubber compounding according to the present invention is not only excellent in reinforcing effect by the epoxy resin cured with phenolic resin but also epoxy resin cured with phenolic resin by adding butadiene-acrylonitrile polymer having a functional group to the sock end. The problem of brittleness was solved, and in addition, the elongation at break and the strength at break were further improved.
    公开号:KR20020092507A
    申请号:KR1020010031155
    申请日:2001-06-04
    公开日:2002-12-12
    发明作者:김현용
    申请人:한국타이어 주식회사；
    IPC主号:
    专利说明:

    Resin Composition for Mixing with Rubber and Rubber Composition Containing the Same}
    [1] The present invention relates to a resin composition for rubber compounding and a rubber composition containing the same, and more particularly, a phenol resin, an epoxy resin having at least two or more epoxy groups in one molecule, and a butadiene-acrylonitrile polymer having a functional group in a sock end. It relates to a rubber composition and a rubber composition containing the same, characterized in that it is included.
    [2] In general, in order to improve reinforcement properties such as hardness and modulus of rubber for tires, high-filling carbon black, a reinforcing filler, or sulfenamide- or thiuram-based compounds, which are sulfur vulcanizing agents and vulcanization accelerators, may be used. A method of increasing or adding a phenol resin which is a reinforcing resin for rubber compounding has been applied.
    [3] The phenolic resin used as the reinforcing resin is divided into two types, a novolak type and a resol type. The novolak type phenol resin is generally used together with a hexamethylene tetramine which is a curing agent.
    [4] However, when phenolic resin is added as a reinforcing resin for rubber compounding, it exhibits high reinforcement, but tends to reduce elongation at break of rubber, thereby deteriorating toughness of rubber. .
    [5] On the other hand, a number of techniques for applying an epoxy resin having excellent mechanical properties as a new reinforcing resin for rubber compounding have been introduced. Such epoxy resins are generally used together with phenolic curing agents.
    [6] Epoxy resin has excellent mechanical properties among thermosetting resins, but shows brittle characteristics, so it was difficult to be used as a reinforcing resin for rubber compounding. Thus, by adjusting and mixing the equivalent ratio of epoxy resin and phenolic resin, An epoxy resin cured with a phenol resin was used as a resin composition for rubber compounding (Japanese Patent Laid-Open No. 2000-154302).
    [7] However, although epoxy resins cured with phenolic resins could further improve the reinforcement of the rubber and also improve the toughness of the rubber by improving the elongation at break, the epoxy resins cured with phenolic resins were also broken. Still had the easy problem.
    [8] In order to solve the fragile problem of the epoxy resin cured with phenolic resin, the present invention provides a rubber compound and a rubber composition containing a rubber compound containing butadiene-acrylonitrile as a rubber component. It is an object to provide a composition.
    [9] In order to achieve the above object, the present invention provides a rubber composition containing a phenol resin, an epoxy resin, and a rubber component butadiene-acrylonitrile polymer, and a rubber composition containing the same.
    [10] Hereinafter, the present invention will be described in detail.
    [11] First, the resin composition for rubber compounding which concerns on this invention is demonstrated.
    [12] The resin composition for rubber compounding according to the present invention contains a phenol resin, an epoxy resin having at least two or more epoxy groups in one molecule, and a butadiene-acrylonitrile polymer having a functional group at the sock end.
    [13] As the phenol resin, a novolak phenol resin or a resol type phenol resin is used. Preferably, the novolak phenol resin is used together with hexamethylene tetramin which is a curing agent.
    [14] Epoxy resins having at least two or more epoxy groups in one molecule include biphenyl epoxy resins, bisphenol epoxy resins, phenol novolak epoxy resins, and cresol novolaks. One or a combination of two or more selected from the group consisting of epoxy resins is used.
    [15] The amount of these phenol resins and epoxy resins can be adjusted according to the required properties, which is such that the ratio of equivalents of hydroxyl groups of phenol resins and equivalents of epoxy groups of epoxy resins has a value between 1: 0.2 and 1: 5.0, preferably It has a value between 1: 0.5 and 1: 2.0.
    [16] If the ratio of the equivalents of hydroxyl groups of the phenol resin and the equivalents of epoxy groups of the epoxy resin is 1: 0.2 or less or 1: 5.0 or more, the ratio difference between the epoxy group of the epoxy resin and the hydroxyl group of the phenol resin is so large that the curing reaction of the epoxy resin and the phenol resin is difficult. It cannot occur efficiently and cannot act as a reinforcing resin.
    [17] In addition, the butadiene-acrylonitrile polymer having a functional group in the sock end may be a butadiene-acrylonitrile having a carboxyl end group (hereinafter, referred to as “carboxyl-terminated-butadiene-acrylonitrile”), a phenol end group Phenol-Terminated Butadiene-Acrylonitrile polymer having, butadiene-acrylonitrile polymer having hydroxyl end groups or butadiene-acrylonitrile having mercaptan end groups -Terminated Butadiene-Acrylonitrile) polymer and the like can be used.
    [18] Butadiene-acrylonitrile polymer improves the toughness of the rubber by introducing functional groups into the sock end as described above. Among the functional groups, the carboxyl group and the phenol group show the most excellent effect on improving the toughness of the rubber. Shows an excellent effect in improving the toughness of the rubber in order of hydroxyl group, mercaptan.
    [19] When the butadiene-acrylonitrile polymer is added to the phenol resin and the epoxy resin, a rubber chain is introduced into the epoxy resin cured with the phenol resin having brittle characteristics, thereby incorporating the rubber according to the present invention. In addition to increasing the flexibility of the resin composition, the compatibility with rubber also increases, so that it is easy to disperse in the rubber matrix when blended with rubber, and is cured with a phenolic resin having excellent mechanical properties and elasticity. The epoxy resin coexists with the sulfur crosslinked structure of the rubber, thereby further improving the reinforcing effect of the rubber.
    [20] This butadiene-acrylonitrile polymer is used in an amount of 2 to 20 parts by weight based on 100 parts by weight of the epoxy resin in the resin composition for rubber compounding according to the present invention.
    [21] A catalyst may be added when preparing the resin composition for rubber compounding according to the present invention, and as the catalyst, triphenylphosphine is preferably used.
    [22] The manufacturing method of the resin composition for rubber compounding containing the phenol resin, an epoxy resin, and butadiene- acrylonitrile polymer demonstrated above is as follows.
    [23] The hydroxyl group of the phenol resin and the epoxy group of the epoxy resin are mixed so as to have an equivalent ratio of 1: 0.2 to 1: 5.0, and the butadiene-acrylonitrile polymer having a functional group at the sock end is 2 to 100 parts by weight of the epoxy resin. 20 parts by weight was added and mixed until a homogeneous solution was obtained at a temperature of about 120 ° C., then the solution was cooled to about 80 ° C., a catalyst was added, and then mixed for about 10 seconds to melt master batch. To manufacture.
    [24] The reason for adding catalyst after cooling to 80 ℃ is that the curing reaction between epoxy resin and phenolic resin requires high temperature, but when the catalyst is added, curing reaction occurs even below 100 ℃. It should be lowered to ℃ and mixed.
    [25] The master batch means that the compounding agent is mixed and kneaded at a higher concentration than the prescription in the process of mixing the compounding agent with the raw material rubber. The melt master batch prepared as described above is mixed with the raw material rubber to form the rubber composition of the present invention. do.
    [26] Next, a rubber composition containing the resin composition for rubber compounding according to the present invention will be described.
    [27] The rubber composition according to the present invention is mixed with 2 to 10 parts by weight of the resin composition for rubber compounding in 100 parts by weight of the raw material rubber, and other reinforcing agents such as carbon black or silica, sulfur as a vulcanizing agent, zinc as a vulcanizing agent and stearic acid and sulfene as a vulcanization accelerator. Conventional additives such as amide accelerators are mixed in the appropriate amounts.
    [28] On the other hand, the raw material rubber is selected from the group consisting of natural rubber, a mixture of natural rubber and diene rubber, and a mixture of natural rubber and diene copolymer rubber.
    [29] Hereinafter, the present invention will be described in more detail based on Examples. However, this invention is not limited by the following Example.
    [30] Example 1 Preparation of Melt Master Batch (I) Containing Epoxy Resin, Phenolic Resin, and Butadiene-Acrylonitrile Polymer
    [31] 10 parts by weight of the CTBN of Formula 3, based on 100 parts by weight of the epoxy resin of the biphenyl-based epoxy resin of Formula 1, and a hydroxyl group of the novolak-type phenol resin of Formula 2, of 1: 1 After mixing until a homogeneous solution was obtained at 120 ° C., the solution was cooled to 80 ° C., and then 1.5 parts by weight of triphenylphosphine of formula 4 as a catalyst was added to 100 parts by weight of an epoxy resin, and then Melt master batch (I) was prepared by mixing for 10 seconds.
    [32] [Formula 1]
    [33]
    [34] [Formula 2]
    [35]
    [36] Wherein n is an integer between 2 and 5.
    [37] [Formula 3]
    [38]
    [39] The CTBN is a compound having a number average molecular weight of 3400 to 4000 and a functionality of 1.8 to 2.3.
    [40] [Formula 4]
    [41]
    [42] Comparative Example 1 Manufacture of Melt Master Batch (II) Containing Epoxy Resin and Phenolic Resin
    [43] Melt master batch (II) was prepared in the same manner as in Example 1 except that CTBN was not used.
    [44] Example 2 Preparation of Rubber Specimens Using a Rubber Composition Containing Melt Master Batch (I)
    [45] Dark brown to yellow ribbed smoke sheet, carbon black, zincated, stearic acid, melt master batch (I) prepared in Example 1, sulfur and A rubber sheet was prepared by kneading a sulfenamide-based accelerator in a half-barrier mixer and then using a two roll mill.
    [46] Then, a tensile test specimen of JIS B-Type was made by cutting a smooth vulcanization test piece of about 2-3 mm with a knife, and a smooth vulcanization test piece of about 2-3 mm was cut into 5 cm x 2 cm using a knife. Cut and chip test specimens were made by cutting and viscoelastic (tanδ) test specimens, and vulcanized in a mold of diameter 5.00 cm, thickness 1.25 cm, and center hole diameter 1.27 cm to make cut and chip test specimens, diameter 6.35 cm, thickness 0.5 cm, and hole diameter 3.0. It was vulcanized in a mold of cm to create a test specimen of rambone wear.
    [47] Comparative Example 2 Preparation of Rubber Specimens Using Rubber Compositions That Do Not Contain Rubber Compositions
    [48] Rubber specimens were prepared in the same manner as in Example 2 except that no melt master batch (I) was used.
    [49] Comparative Example 3 Preparation of Rubber Specimen Using Rubber Composition Containing Only Phenol Resin
    [50] A rubber specimen was prepared in the same manner as in Example 2, except that 3 parts by weight of novolak-type phenol resin and 3 parts by weight of hexamethylene tetramin were used instead of the melt master batch (I).
    [51] Comparative Example 4 Preparation of Rubber Specimen Using Rubber Composition Containing Melt Master Batch (II)
    [52] A rubber specimen was prepared in the same manner as in Example 2 except for using 6 parts by weight of the melt master batch (II) instead of the melt master batch (I).
    [53] TABLE 1
    [54] Comparative Example 2Comparative Example 3Comparative Example 4Example 2 Natural rubber100100100100 Carbon black (ISAF)50505050 Zincification3333 Stearic acid2222 Hexamethylene tetramine-3-- Novolac Type Phenolic Resin-3-- MMB I---6 MMB II--6- brimstone2222 Sulfenamide type acceleratorOneOneOneOne 1) Unit: parts by weight 2) Carbon Black (ISAF: Intermediate Super Abrasion Furnace): Semi-ultra wear-resistant carbon black
    [55] Experimental Example
    [56] In the experimental example, some physical properties of the rubber specimens prepared in Example 2 and Comparative Examples 2 to 4 were measured, and the results are shown in Table 2.
    [57] TABLE 2
    [58] Comparative Example 2Comparative Example 3Comparative Example 4Example 2 Hardness65687270 300% modulus (㎏ / ㎠)110130140130 Elongation at Break (%)520480470 525 Breaking Strength (㎏ / ㎠)250255250260 Rambon wear (cc)0.410.350.340.32 Cut & Chip (cc)0.980.900.890.85 Tanδ (60 ° C)0.1180.1150.1000.112
    [59] At this time, hardness was measured by ASTM Shore A method, and tensile test, 300% modulus, elongation at break and breaking strength, were used by Universal Tester made by Instron using JIS B-Type tensile test specimen and the moving speed of clamp was 500mm / min. It was measured by.
    [60] The 300% modulus value was derived by Equation 1 below.
    [61] [Equation 1]
    [62] 300% modulus = Fn / A
    [63] In this case, Fn represents the load (kg) at 300% elongation and A represents the cross-sectional area (cm 2) of the specimen.
    [64] Elongation at break was derived by Equation 2 below.
    [65] [Equation 2]
    [66] Elongation at Break = (L 1 -L 0 ) / L 0 × 100
    [67] At this time, L 0 represents the initial length (mm) of the specimen, L 1 represents the length (mm) at the time of fracture of the specimen.
    [68] Breaking strength was derived by Equation 3 below.
    [69] [Equation 3]
    [70] Breaking Strength = F / A
    [71] In this case, F represents the load (kg) at break with the maximum load of the specimen, and A represents the cross-sectional area (cm 2) of the specimen.
    [72] In addition, the rambon wear was measured under a condition of 25% slip using a rambon abrasion tester, tanδ was measured at a strain rate of 0.5% and a frequency of 10Hz while raising the temperature using a twist type tester, and the cut & chip was a BF Goodrich tester. The rotational speed of the test piece was measured at 750 rpm and the speed of the cutting knife was measured at 10 rpm for 10 minutes.
    [73] As can be seen in Table 2, the rubber specimen of Example 2 made of a rubber composition containing the resin composition of the present invention was improved in elongation and fracture strength at break when compared with the rubber specimens of Comparative Examples 2 to 4 , Cut & Chip value is lowered.
    [74] As described above, the resin composition for rubber compounding according to the present invention is not only excellent in reinforcing effect by the epoxy resin cured with phenol resin, but also the addition of butadiene-acrylonitrile polymer having a functional group to the sock end of the rubber component. The fragile problem of the epoxy resin cured with phenolic resin has been solved, and the elongation at break and the strength at break can be further improved.
    权利要求:
    Claims (5)
    [1" claim-type="Currently amended] A resin composition for rubber blending, comprising a phenol resin, an epoxy resin having at least two or more epoxy groups in one molecule, and a butadiene-acrylonitrile polymer having a functional group at the sock end.
    [2" claim-type="Currently amended] The method of claim 1,
    The butadiene-acrylonitrile polymer having a functional group at the sock end is a carboxyl-terminated butadiene-acrylonitrile polymer having a carboxyl end group and a phenol end group butadiene-acrylonitrile having a phenol end group. Acrylonitrile) polymer, Hydroxyl-Terminated Butadiene-Acrylonitrile polymer with hydroxyl end groups, and butadiene-acrylonitrile (Mercaptan-Terminated Butadiene-Acrylonitrile) polymer with mercaptan end groups A resin composition for rubber compounding, characterized in that one or two or more combined.
    [3" claim-type="Currently amended] The method of claim 1,
    Butadiene-acrylonitrile polymer having a functional group in the sock end is a resin composition for rubber compounding, characterized in that contained 2 to 20 parts by weight based on 100 parts by weight of the epoxy resin.
    [4" claim-type="Currently amended] The method of claim 1,
    Equivalent ratio of the hydroxyl group of the phenol resin and the epoxy group of the epoxy resin is a value between 1: 0.2 to 1: 5.0, the resin composition for rubber compounding.
    [5" claim-type="Currently amended] Raw rubber selected from the group consisting of natural rubber, a mixture of natural rubber and diene rubber, and a mixture of natural rubber and diene copolymer rubber; 2 to 10 parts by weight of the resin composition for rubber compounding according to claim 1, based on 100 parts by weight of the raw material rubber; And at least one additive selected from the group consisting of reinforcing agents, vulcanizing agents, vulcanizing agents and vulcanizing accelerators.
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    同族专利:
    公开号 | 公开日
    KR100437322B1|2004-06-25|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2001-06-04|Application filed by 한국타이어 주식회사
    2001-06-04|Priority to KR10-2001-0031155A
    2002-12-12|Publication of KR20020092507A
    2004-06-25|Application granted
    2004-06-25|Publication of KR100437322B1
    优先权:
    申请号 | 申请日 | 专利标题
    KR10-2001-0031155A|KR100437322B1|2001-06-04|2001-06-04|Resin Composition for Mixing with Rubber and Rubber Composition Containing the Same|
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