Patent Application
20130331523
The present invention relates to a tread compound comprising trialkoxymercaptoalkyl-silanes.
In certain compounds, such as tread compounds, silica has long been substituted for conventional carbon black as a reinforcing filler, because of its advantages in terms of rolling resistance and wet road-holding performance.
Silica is used in combination with silane coupling agents, which bond with silanol groups to prevent the formation of hydrogen bonds between silica particles, and at the same time bond the silica chemically to the polymer base.
As silane coupling agents, mercaptoalkyl-silanes have recently been found to further improve compounds in terms of both rolling resistance and hydrocarbon emissions.
The following, in particular, has proved highly effective:
SH(CH2)3Si(OCH2CH3)(O(CH2CH2O)5(CH2)13CH3)2
Alongside the above advantages, however, trialkoxymercaptoalkyl-silanes have the drawbacks of increasing the viscosity of the compound, and so making it harder to process, impairing wet road-holding performance, and reducing abrasion resistance. One attempt to solve these problems has been to use large-area (170-230 m2/g) silica. This, however, while improving wet road-holding performance and abrasion resistance, has been found to increase viscosity and so further compound viscosity-related problems.
It is an object of the present invention to provide a compound enabling silane coupling agents in the trialkoxymercaptoalkyl-silane class to be used in conjunction with large-area silica, without incurring processing problems, and without compromising other significant characteristics of the compound.
According to the present invention, there is provided a method of producing a rubber compound, comprising a first mixing step of mixing at least one cross-linkable unsaturated-chain polymer base, silica, and a silane coupling agent in the mercaptoalkyl-silane class; and a final mixing step, in which a curing system is added to the mix; said method being characterised in that said silane coupling agent is used in adsorbed form on dibenzothiazyl disulphide.
Preferably, at said first mixing step, the mix comprises 10 to 100 phr of silica with a superficial area of 170 to 230 m2/g.
Preferably, at said first mixing step, the mix comprises 1 to 20 phr of a silane coupling agent in the trialkoxymercaptoalkyl-silane class.
Preferably, said silane coupling agent is used in adsorbed form on 0.5 to 6 phr of said dibenzothiazyl disulphide.
Preferably, said silane coupling agent is also used in adsorbed form on 5 to 10 phr of carbon black.
Preferably, said silane coupling agent has the formula (I)
R1R22Si—R3—SH (I)
where:
R1 represents a linear, cyclic or branched alkoxyl group with 1 to 8 carbon atoms; R2 represents a linear, cyclic or branched alkoxyl group with 1 to 8 carbon atoms, or —O—(Y—O)m4-X (where Y represents a linear, cyclic or branched saturated or unsaturated divalent hydrocarbon group with 1 to 20 carbon atoms, X represents a linear, cyclic or branched alkyl group with 1 to 9 carbon atoms, and m4 represents a number of 1 to 40); and R3 represents a linear, cyclic or branched saturated or unsaturated alkylene group with 1 to 12 carbon atoms.
Preferably, said silane coupling agent is in the trialkoxymercaptopropyl-silane class.
Preferably, said silane coupling agent has the formula (II)
SH(CH2)3SiR4R52 (II)
where:
R4 is —OCH2CH3, and
R5 is —O(CH2CH2O)5(CH2)13CH3
The following are non-limiting examples for a clearer understanding of the invention.
Three control compounds (A-C) and one compound (D) in accordance with the teachings of the present invention were produced. More specifically, a first control compound (A) is one in accordance with the known art, employing a silane coupling agent not in the trialkoxymercaptoalkyl-silane class; a second control compound (B) is the same as the first, but employing a silane coupling agent in the trialkoxymercaptoalkyl-silane class; and the third control compound (C) is the same as the second, but employing large-area silica.
The compounds were produced as follows:
First Mixing Step—
Before commencing the mixing operation, a 230-270-litre tangential-rotor mixer was loaded with the cross-linkable unsaturated-chain polymer base, the silica, the carbon black, and the silane coupling agent to a fill factor of 66-72%.
In compound D according to the invention, the silane coupling agent was added in adsorbed form on all the carbon black and on dibenzothiazyl disulphide (MBTS).
The mixer was operated at a speed of 40-60 rpm, and the resulting mix was unloaded on reaching a temperature of 140-160° C.
Second Mixing Step—
The mix from the first step was mixed again in a mixer operated at 40-60 rpm, and was unloaded on reaching a temperature of 130-150° C.
Third Mixing Step—
The curing system and zinc oxide were added to the mix from the second step to a fill factor of 63-67%.
The mixer was operated at a speed of 20-40 rpm, and the resulting mix was unloaded on reaching a temperature of 100-110° C.
Compound Compositions—
Table I shows the compound compositions in parts by weight per hundred parts of total polymer base.
Silica1 is marketed by EVONIK as VN3, and has a surface area of 170 m2/g.
Silica2 is marketed by RHODIA as MP200, and has a surface area of 210 m2/g and 55 nm particle size.
Silane coupling agent1 is marketed by DEGUSSA as S175.
Silane coupling agent2 is the mercaptosilane of formula I indicated above.
Laboratory Test Results—
The above compounds were tested to determine a number of particularly significant parameters.
Table II shows the test results of each parameter for each compound.
The parameters tested were:
Mooney Scorch at 130° C. as per ASTM Standard D1646;
elasticity modulus (E′) and Tanδ as per ASTM Standard D5992, from which wet road-holding and rolling resistance were extrapolated and indexed with respect to compound A;
abrasion resistance as per DIN Standard 53516, and indexed with respect to compound A;
viscosity (ML1′+4′ at 130° C.) as per ASTM Standard D1646, and indexed with respect to compound A.
The values in Table II are indexed with respect to a value of 100 for compound A.
As shown in Table II, the method according to the invention (compound D) enables silane coupling agents in the trialkoxymercaptoalkyl-silane class to be used in conjunction with large-area silica, without high viscosity compromising the workability of the compound.
As the scorch values show, though MBTS is normally used as an accelerant and so added at the third mixing step, using it at the first mixing step as an adsorbed silane coupling agent support in no way affects curing speed.
| Number | Date | Country | Kind |
|---|---|---|---|
| TO2010A001056 | Dec 2010 | IT | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/IB2011/055953 | 12/23/2011 | WO | 00 | 8/13/2013 |
