Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – At least one aryl ring which is part of a fused or bridged...
Reexamination Certificate
2000-06-08
2004-06-22
Toomer, Cephia D. (Department: 1714)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
At least one aryl ring which is part of a fused or bridged...
C524S392000, C524S201000, C523S152000, C152S209100
Reexamination Certificate
active
06753374
ABSTRACT:
BACKGROUND OF THE INVENTION
This invention relates generally to rubber compositions and a method for increasing the Mooney Scorch value of a rubber composition. More particularly, the rubber composition described herein contains at least (a) a rubber component; (b) a silica filler, and, (c) at least one thiuram disulfide accelerator which increases the silica associated properties. The rubber compositions are particularly useful for tire tread applications in vehicles, e.g., passenger automobiles and trucks.
The tire treads of modern tires must meet performance standards which require a broad range of desirable properties. Thus, rubber compositions suitable for, e.g., tire treads, should exhibit not only desirable strength and elongation, particularly at high temperatures, but also good cracking resistance, good abrasion resistance, desirable skid resistance and low tan delta values at low frequencies for desirable rolling resistance. Additionally, a high complex dynamic modulus is necessary for maneuverability and steering control.
Major tire manufacturers have developed tire tread compounds which provide lower rolling resistance for improved fuel economy and better skid/traction for a safer ride. Three types of performance are important in tread compounds. They include good wear resistance, good traction and low rolling resistance.
Presently, silica has been added to rubber compositions as a filler to replace some or substantially all of the carbon black filler to improve these properties, e.g., lower rolling resistance. Although more costly than carbon black, the advantages of silica include, for example, improved wet traction, low rolling resistance, etc., with reduced fuel consumption. Problems associated with the use of silica include processing difficulties and reduced wear. The wear reduction is believed to be associated with the less uniform silica dispersion properties and decreased reinforcement characteristics of silica as compared with carbon black.
The difficulties in dispersing silica are believed to be associated with the polar nature of silica and non-polar nature of rubber. Regardless, the silica has been found to form localized clumps or aggregations in the rubber which detract from both tire wear and fuel consumption. As compared with carbon black, silica does not react as strongly with the rubber and thereby tends to give less strength to the rubber.
It is known to use coupling agents to enhance the rubber reinforcement characteristics of silica A coupling agent is a bi-functional molecule that will react with the silica at one end thereof and cross-link with the rubber at the other end thereof. In this manner, the reinforcement and strength of the rubber are improved, e.g. the toughness, strength, modulus, tensile and abrasion resistance are particularly improved. The coupling agent is believed to cover the surface of the silica particle which then hinders the silica from agglomerating with other silica particles. By interfering with the agglomeration process, the dispersion is improved and therefore the wear and fuel consumption are improved.
The use of silica in relatively large proportions for improving various tire properties has been found to undesirably slow the cure rate of the rubber. This has led to the use of secondary accelerators such as diphenyl guanidine (DPG) in amounts which increase the cure rate. These accelerators are typically used in combination with other accelerators such as sulfenamides.
However, the use of these secondary accelerators, and particularly DPG, typically result in the rubber composition possessing a lower Mooney scorch value during its manufacture thereby resulting in decreased processing time. Problems associated with a decreased processing time include, for example, precured compounds and rough surfaces on extruded parts. Additionally, diphenyl guanidine is typically employed in high amounts which result in the rubber compositions being more expensive to manufacture since more material must be used.
SUMMARY OF THE INVENTION
In accordance with the present invention a rubber composition is provided which comprises (a) a rubber component; (b) a silica filler; and, (c) at least one thiuram disulfide accelerator, it being provided that diphenyl guanidine is substantially absent in the rubber composition.
By employing a thiuram disulfide in place of diphenyl guanidine in a rubber composition, the rubber compositions disclosed herein advantageously possess a higher Mooney Scorch value relative to a rubber composition containing diphenyl guanidine. This allows for a longer processing time of the rubber which, in turn, provides for further manufacturing of the rubber. Additionally, significantly lower amounts of the thiuram disulfides can be employed in the rubber compositions described herein relative to the amounts of which diphenyl guanidine has been used in rubber compositions thereby providing an economical advantage by using less materials.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The rubber compositions of this invention contains at least (a) a rubber component; (b) a silica filler, and, (c) at least one thiuram disulfide accelerator, it being provided that diphenyl guanidine is substantially absent in the rubber composition.
The rubber components for use herein are based on highly unsaturated rubbers such as, for example, natural or synthetic rubbers. Representative of the highly unsaturated polymers that can be employed in the practice of this invention are diene rubbers. Such rubbers will ordinarily possess an iodine number of between about 100 to about 250, although highly unsaturated rubbers having a higher or a lower (e.g., of 50-100) iodine number can also be employed. Illustrative of the diene rubbers that can be utilized are polymers based on conjugated dienes such as, for example, 1,3-butadiene; 2-methyl-1,3-butadiene; 1,3-pentadiene; 2,3-dimethyl-1,3-butadiene; and the like, as well as copolymers of such conjugated dienes with monomers such as, for example, styrene, alpha-methylstyrene, acetylene, e.g., vinyl acetylene, acrylonitrile, methacrylonitrile, methyl acrylate, ethyl acrylate, methyl methacrylate, ethyl methacrylate, vinyl acetate, and the like. Preferred highly unsaturated rubbers include natural rubber, cis-polyisoprene, polybutadiene, poly(styrene-butadiene), styrene-isoprene copolymers, isoprene-butadiene copolymers, styrene-isoprene-butadiene tripolymers, polychloroprene, chloro-isobutene-isoprene, nitrile-chloroprene, styrene-chloroprene, and poly (acrylonitrile-butadiene). Moreover, mixtures of two or more highly unsaturated rubbers with elastomers having lesser unsaturation such as EPDM, EPR, butyl or halogenated butyl rubbers are also within the contemplation of the invention.
Suitable silica fillers include silica, precipitated silica, amorphous silica, vitreous silica, fumed silica, fused silica, synthetic silicates such as aluminum silicates, alkaline earth metal silicates such as magnesium silicate, calcium silicate and the like with BET surfaces of 20 to 400 m
2
/g and primary particle diameters of 10 to 400 nm, natural silicates such as kaolin and other naturally occurring silicas and the like. Also useful are highly dispersed silicas prepared, for example, by precipitation of solutions of silicates or by flame hydrolysis of silicon halides with specific surfaces of 5 to 1000 m
2
/g and preferably 20 to 400 m
2
/g (BET surface) with primary particle sizes of 100 to 400 nm. The silicas can also be present in the form of mixed oxides with other metal oxides such as Al, Mg, Ca, Ba, Zn, Zr, Ti oxides and the like. Silicas are commercially available from such sources as Cabot Corporation under the Cab-O-Sil® tradename; PPG Industries under the Hi-Sil and Ceptane tradenames; Rhodia under the Zeosil tradename and Degussa AG under the Ultrasil and Coupsil tradenames. Mixtures of two or more silica fillers can be used in preparing the rubber composition of this invention. A preferred silica for use herein is Zeosil 1165MP manufactured by Rhodia.
Generally, the silica filler is incorporated i
Cornell Robert J.
Hannon Martin J.
Hong Sung W.
Reitenbach Daniel
Toomer Cephia D.
Uniroyal Chemical Company, Inc.
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