WIRE COAT RUBBER COMPOSITION FOR A TIRE AND A TIRE COMPRISING A WIRE COAT RUBBER COMPOSITION
20200399448 ยท 2020-12-24
Inventors
- Julia Martine Francoise Claudine Tahon (Reckange, LU)
- Robert Anthony Bethea (Cincinnati, OH, US)
- James Joseph Golden (North Canton, OH, US)
- Carolin Anna WELTER (Schleich, DE)
- Christian Jean-Marie Kaes (Schrondweiler, LU)
Cpc classification
C08L9/00
CHEMISTRY; METALLURGY
C09D107/00
CHEMISTRY; METALLURGY
B60C2009/0021
PERFORMING OPERATIONS; TRANSPORTING
B60C1/00
PERFORMING OPERATIONS; TRANSPORTING
C08L2205/03
CHEMISTRY; METALLURGY
B29D2030/383
PERFORMING OPERATIONS; TRANSPORTING
B29D30/38
PERFORMING OPERATIONS; TRANSPORTING
B60C2001/0066
PERFORMING OPERATIONS; TRANSPORTING
B29D2030/381
PERFORMING OPERATIONS; TRANSPORTING
C08L9/00
CHEMISTRY; METALLURGY
International classification
Abstract
In accordance with the invention a wire coat rubber composition for a tire comprises from 70 phr to 100 phr of cis 1,4-polyisoprene rubber, from 0 phr to 30 phr of solution styrene butadiene rubber, from 65 phr to 95 phr pre-silanized precipitated silica, from 0.1 phr to 5 phr of a cobalt salt, up to 15 phr carbon black, up to 10 phr of a resin, and up to 10 phr oil. Further the present invention is directed to a tire comprising such a wire coat composition.
Claims
1. A wire coat rubber composition comprising: 70 phr to 100 phr of cis 1,4-polyisoprene rubber, up to 30 phr of solution styrene-butadiene rubber, 65 phr to 95 phr pre-silanized precipitated silica, 0.1 phr to 5 phr of a cobalt salt, up to 15 phr carbon black, up to 10 phr of a resin, and up to 10 phr oil.
2. The wire coat rubber composition of claim 1, wherein the cobalt salt is present at a level which is within the range of 0.2 phr to 2 phr.
3. The wire coat rubber composition of claim 1, further comprising from 1 to 20 phr zinc oxide.
4. The wire coat rubber composition of claim 1 further comprising from 1 to 15 phr sulfur.
5. The wire coat rubber composition of claim 1, wherein the level of resin in the composition is less than 5 phr.
6. The wire coat rubber composition of claim 1, wherein the pre-silanized precipitated silica has a CTAB adsorption surface area which is within the range of 130 m.sup.2/g to 210 m.sup.2/g.
7. The wire coat rubber composition of claim 1, wherein said pre-silanized precipitated silica is precipitated silica pre-reacted with a silica coupler comprised of bis(3-triethoxysilylpropyl)polysulfide containing an average of from 1 to 5 connecting sulfur atoms in its polysulfidic bridge or an alkoxyorganomercaptosilane.
8. The wire coat rubber composition of claim 1, wherein said pre-silanized precipitated silica is pre-hydrophobated with a hydrocarbon chain material with at least 4 carbon atoms along its chain length.
9. The wire coat rubber composition of claim 1, wherein the wire coat rubber composition contains less than 5 phr oil.
10. The wire coat rubber composition of claim 1, wherein the solution styrene-butadiene rubber is present at a level which is within the range of 10 phr to 25 phr; and wherein the solution styrene-butadiene rubber has a glass transition temperature which is within the range of 30 C. and 90 C.
11. The wire coat rubber composition of claim 10, wherein the solution styrene butadiene rubber has a glass transition temperature which is within the range of 50 C. and 70 C. and wherein the solution styrene-butadiene rubber is tin-coupled.
12. The wire coat rubber composition of claim 10, wherein the solution styrene-butadiene rubber is thio-functionalized.
13. The wire coat rubber composition of claim 10, wherein the solution styrene-butadiene rubber has a bound styrene content which is within the range of 10% to 20%, and a vinyl content which is within the range of 20% to 40%.
14. The wire coat rubber composition of claim 1 wherein the cis 1,4-polyisoprene rubber is present at a level which is within the range of 75 phr to 90 phr, wherein the solution styrene-butadiene rubber is present at a level which is within the range of 10 phr to 25 phr, and wherein the pre-silanized precipitated silica is present at a level which within the range of from 70 phr to 90 phr.
15. The wire coat rubber composition of claim 1 wherein the cis 1,4-polyisoprene rubber is present at a level which is within the range of 90 phr to 100 phr, wherein the pre-silanized precipitated silica is present at a level which is within the range of 70 phr to 90 phr, wherein the carbon black is present at a maximum level of 10 phr, and wherein the resin is present at a maximum level of 5 phr.
16. A pneumatic tire which is comprised of a generally toroidal-shaped carcass with an outer circumferential tread, two spaced beads, at least one reinforced ply extending from bead to bead, and sidewalls extending radially from and connecting said tread to said beads, wherein said tread is adapted to be ground-contacting, and wherein the tire further includes metal reinforcing wires which are embedded in the wire coat rubber composition of claim 1.
17. The pneumatic tire as specified in claim 16 wherein metal reinforcing wires are embedded in the reinforced ply which is comprised of a plurality of essentially metal wires which are spaced apart from one another and extend essentially in parallel to each other.
18. The pneumatic tire as specified in claim 17 wherein metal wires are calendared on both sides with the rubber composition.
19. The pneumatic tire of claim 16 wherein the metal reinforcing wires are embedded in ply strips.
20. The pneumatic tire of claim 17 wherein the wherein the pre-silanized precipitated silica has a CTAB adsorption surface area which is within the range of 130 m.sup.2/g to 210 m.sup.2/g; wherein said pre-silanized precipitated silica is precipitated silica pre-reacted with a silica coupler comprised of bis(3-triethoxysilylpropyl)polysulfide containing an average of from 1 to 5 connecting sulfur atoms in its polysulfidic bridge or an alkoxyorganomercaptosilane; wherein said pre-silanized precipitated silica is pre-hydrophobated with a hydrocarbon chain material with at least 4 carbon atoms along its chain length; and wherein the wire coat rubber composition contains less than 5 phr oil.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0066] The structure, operation, and advantages of the invention will become more apparent upon contemplation of the following description taken in conjunction with the accompanying drawings, wherein:
[0067]
[0068]
DETAILED DESCRIPTION OF THE EMBODIMENTS
[0069]
[0070] While the embodiment of
[0071] The schematic cross-section of
[0072] Metal wires 15 may be coated with brass for better adhesion properties with regards to connection of the wires 15 to the cured rubber composition 20. The wires 15 may also be dipped in dipping solutions or emulsions for better adhesion properties as known in the art. Neither a dip nor a metal coating is shown here in
[0073] While the schematic drawing of
[0074] Preferred examples of the rubber composition are shown in Table 1 in comparison with a Control sample. The control sample comprises carbon black as a filler material whereas the compounds according to the invention comprise pre-silanized precipitated silica. Moreover, the first example comprises a significant amount of an SSBR whereas the control and the second example each comprise 100 phr natural rubber. Moreover, the first and second examples comprise also a resin system of reactive resins and higher amounts of accelerators and antidegradants than the control sample.
TABLE-US-00001 TABLE 1 Parts by weight (phr) Inventive Inventive Material Control Example 1 Example 2 Natural rubber 100 83 100 Carbon Black 60 0 0 SSBR.sup.1 0 17 0 Pre-silanized Precipitated Silica.sup.2 0 80 80 Zinc Oxide 10 8 8 Resin.sup.3 0 2.5 2.5 0i1.sup.4 1 1 1 Antidegradants 2 3 3 Stearic Acid 0 1 1 Cobalt Salt 0.5 0.5 0.5 Accelerator.sup.5 1 1.5 1.5 Sulfur 5 5 5 .sup.1SSBR as Sprintan SLR 3402 of the company Trinseo having a T.sub.g of about 62 C. .sup.2Pre-silanized (pre-hydrophobated) precipitated silica as Agilon 400 from PPG Industries as precipitated silica chemically treated with an alkoxyorganomercaptosilane .sup.3Resin system comprising a phenol formaldehyde reactive type resin and a hexamethoxymethylmelamine .sup.4Naphthenic oil .sup.5Sulfur cure accelerators as sulfenamide
[0075] Table 2 discloses mechanical test results for the control composition and the example compositions disclosed in Table 1. Shore A hardness of both inventive examples has increased over the control sample. Rebound values have also increased significantly by more than 5% over the control sample. Rebound can be a good indicator for stiffness/hysteresis ratio. G at 1% and G at 15% have also increased significantly in the order of 50% for both inventive examples. While tangent delta values have increased for Example 1, it remains flat for example 2 in comparison with the control sample. Modulus values at 100% and 200% keep roughly the level of the control. Elongation at break values have increased. Tensile strength has also increased when comparing the inventive examples with the control sample. The improvement in the rebound test values as well as the improvement in the G and shore A hardness values, indicating a high compound stiffness, predict together also an improvement of the component's hysteresis behavior which has also a positive influence on rolling resistance.
TABLE-US-00002 TABLE 2 Inventive Inventive Test/Property Units Control Example 1 Example 2 Shore A hardness(23 C.) .sup.a 70.1 72.6 71.5 Rebound(23 C.) .sup.b % 48.38 52.1 50.27 G (1%) .sup.c MPa 2.78 4.41 4.6 G (15%) .sup.c MPa 1.48 2.25 2.08 Tan delta (10%) .sup.c 0.15 1.3 0.15 Modulus (100%) .sup.d MPa 3.7 3.1 3.7 Modulus (200%) .sup.d MPa 9.6 9.4 7.7 Elongation at break .sup.d % 316 365 490 Tensile strength .sup.d MPa 16.0 17.0 20.0 .sup.a Shore A hardness measured according to ASTM D2240. .sup.b Rebound measured on a Zwick Roell 5109 rebound resilience tester according to DIN 53512/ASTM D1054 at given temperature. .sup.c Data obtained with an RPA 2000 Rubber Process Analyzer of Alpha Technologies based on ASTM D5289. .sup.d Ring sample test based on ASTM D412 and DIN 53504, percentages are percentages of elongation, respectively strain; tensile strength is stress at break; elongation is elongation at break in %.
[0076] The amounts of materials are usually expressed in parts of material per 100 parts of rubber by weight (phr).
[0077] If an amount of ingredient is mentioned with up to herein, this shall include also the option of 0 (zero) phr of that ingredient or from 0 to.
[0078] Variations in the present invention are possible in light of the provided description. While certain representative embodiments, examples and details have been shown for the purpose of illustrating the subject invention, it will be apparent to those skilled in this art that various changes and modifications can be made therein without departing from the scope of the invention. It is, therefore, to be understood that changes may be made in the particular example embodiments described which will be within scope of the invention as defined by the following appended claims.
[0079] In any case the above described embodiments and examples shall not be understood in a limiting sense. In particular, the features of the above embodiments may also be replaced or combined with one another.