Patent Application
20060128868
This invention relates to tires wherein at least a portion of its tire tread containing a running surface is of a rubber composition comprised of a functionalized elastomer, silica reinforcement, particularly precipitated silica aggregates which contain hydroxyl groups (e.g. silanol groups) and a blocked alkoxyorganomercaptosilane coupling agent. The rubber composition may constitute the entire, or major portion of, the running surface of the tread or may be limited to only a longitudinal circumferential strip, or portion, of the running surface of the tread. Such functionalized elastomer is an elastomer which contains functional groups distributed along the polymer chain and/or at its terminal end. Such functional groups may be divided into two categories, namely, a first category which promotes adsorptive interactions with the precipitated silica and a second category which chemically bonds to the precipitated silica. Such functionalized elastomer may contain functional group(s) from either of both of said first and second categories. In addition, said functionalized elastomer may be tin coupled.
Tire treads are sometimes composed of a rubber composition comprised of conjugated diene-based elastomers which contain particulate synthetic amorphous silica reinforcement, particularly precipitated silica aggregates which contain hydroxyl groups (e.g. silanol groups) on their surface.
The hydroxyl groups (e.g. silanol groups) on the silica aggregates may be in a form of, for example, isolated and geminal hydroxyl groups. When blended with elastomers (e.g. conjugated diene-based elastomers) the silanol groups tend to promote an undesirable aggregation (agglomeration) of the silica aggregates generally thought to be caused by hydrogen bond formation between hydroxyl groups (e.g. silanol groups) of neighboring silica aggregates.
Such agglomeration of the silica aggregates may be attenuated, for example, by utilization of functionalized elastomers which contain functional groups which can interact with the hydroxyl groups (silanol, or SiOH, groups) to reduce their capacity to agglomerate.
Such functional groups, in general and depending somewhat upon the functional group and conjugated diene-based elastomer, may be positioned anywhere along the elastomer chain, in a form of, for example, a random distribution of the functional groups, small blocks of the functional group and/or said functional groups may be positioned on a terminal end of the elastomer chain. In general, for most functional groups, it is believed to be well known to those having skill in such art that elastomers which contain such a functional group on its terminal end are particularly beneficial to impart various desirable physical characteristics to the resulting silica reinforced rubber composition for use, for example, as a pneumatic tire tread.
However, use of such functionalized conjugated diene-based elastomers typically renders an increased processing difficulty in a form of significantly increased viscosity of the associated rubber composition (e.g. significantly higher Mooney ML viscosity) when used in combination with a reinforcing filler of precipitated silica aggregates which may particularly be evident when a sulfur liberating silica coupling agent is present. As a result, the rubber composition with its included ingredients typically becomes progressively more difficult to mix in an internal rubber mixer. In addition, the shaping of the resulting unvulcanized rubber composition, such as by for example extrusion and calendering, also becomes more difficult in a sense of obtaining a smooth surfaced product.
Such processing difficulty is typically amplified when the precipitated silica aggregates are blended with the functional elastomer in combination with a silica coupling agent which contains a first moiety which reacts with the hydroxyl groups (e.g. silanol groups) of the precipitated silica aggregates and a second moiety which interacts with the diene-based elastomer during one or more mixing phases, or steps, of the rubber composition, particularly in an internal rubber mixer.
For example, such first moiety may, for example, be an alkoxysilane which typically relatively quickly reacts with the hydroxyl groups of the silica aggregates. Such second moiety may, for example, be a polysulfide or mercapto group which provides liberated sulfur groups which, in turn, interact with the diene-derived portion of the elastomer(s) which may significantly increase the viscosity of the uncured rubber composition to thereby adversely affect its processability as it is being mixed and/or extruded to form a shaped unvulcanized rubber article such as, for example, tire tread strip.
It is a significant aspect of the present invention to utilize such functionalized elastomers in combination with precipitated silica aggregates together with a silica coupling agent in a manner which promotes a more processable unvulcanized rubber composition.
Historically, a prospect of using a silica coupling agent in a form of a blocked alkoxyorganomercaptosilane which has been chemically blocked to delay the interaction of such second moiety of the coupling agent with a diene-based elastomer is suggested in PCT/US98/17391 and U.S. Pat. No. 3,692,812. However, the prospect is not contemplated therein of preparing a precipitated silica aggregate reinforced rubber composition comprised of one or more of the aforesaid functionalized elastomers.
The blocked mercaptoalkoxysilane coupling agent for this invention is composed of an alkoxyorganomercaptosilane where the hydrogen moiety of the mercaptan moiety is substituted with a blocking moiety which allows the alkoxy groups of the mercaptoalkoxyosilane to proceed to react with the precipitated silica having hydroxyl groups (e.g. silanol groups) on its surface yet renders the mercapto portion of the mercaptoalkoxysilane relative inert, insofar as interaction with the diene-based elastomer(s) is concerned, until the blocked mercapto portion of the alkoxyorganomercaptosilane becomes unblocked.
Therefore the coupling action of the alkoxyorganomercaptosilane is interrupted by disconnecting the initial reaction of its alkoxysilane portion with the silica from the interaction of the mercapto portion with the diene-based elastomer(s) and particularly with the aforementioned specialized elastomer(s). Upon subsequent unblocking of the blocked mercapto moiety of the alkoxyorganomercaptosilane within the rubber composition during the subsequent vulcanization of the rubber composition at an elevated temperature, the silica becomes coupled via the mercapto group of the mercaptoalkoxysilane to one or more elastomers of the rubber composition.
In the description of this invention, the term “phr” relates to parts by weight for a material or ingredient per 100 parts by weight elastomer(s)”. The terms “rubber” and “elastomer” may be used interchangeably unless otherwise indicated. The terms “cure” and “vulcanize” may be used interchangeably unless otherwise indicated.
In accordance with this invention, a tire is provided having a circumferential tread wherein a running surface of the tread is of a rubber composition comprised of, based upon parts by weight per 100 parts by weight of elastomers (phr):
(A) about 10 to about 100, alternatively from about 50 to about 80, phr of at least one functionalized elastomer comprised of a conjugated diene-based elastomer functionalized with at least one functional group,
wherein said diene-based elastomer is selected from at least one polymer of at least one of isoprene and 1,3-butadiene and copolymers of styrene with at least one of isoprene and 1,3-butadiene,
wherein said functional group(s) are positioned on said diene-based elastomer (e.g. along the length of the elastomer chain) and/or positioned on a terminal end of said diene-based elastomer,
wherein said functional groups are comprised of a first category, second category or combination thereof,
wherein said categories of said functional groups are composed of:
(B) from zero to about 90, alternately from about 20 to about 50, phr of at least one additional conjugated diene-based elastomer (other than and in addition to said functionalized diene-based elastomers) selected from at least one polymer of at least one of isoprene and 1,3-butadiene and copolymers of styrene with at least one of isoprene and 1,3-butadiene;
(C) from about 30 to about 110, alternately from about 30 to about 80, phr of reinforcing filler as:
(D) a silica coupling agent as a blocked alkoxyorganomercaptosilane:
In further accordance with this invention, said functionalized conjugated diene-based elastomer may be tin coupled, and therefore contain a tin group, which may promote an improvement in the interaction between the functionalized elastomer and rubber reinforcing carbon black fillers. Such tin coupling may, for example, be accomplished by terminating the polymerization of the monomers for the said functionalized conjugated diene-based elastomer in an organic solvent polymerization system with a tin compound such as for example tin tetrachloride (SnCl4), a procedure well known to those having skill in such art. For example, said functionalized elastomer may be tin coupled to significantly increase its molecular weight wherein the tin coupled elastomer can then decouple at the tin functional group position during the processing of the rubber composition (e.g. high shear mixing in an internal rubber mixer), which results in a reduction of the tin coupled functionalized elastomer's molecular weight and viscosity (e.g. Mooney viscosity). Representative of additional tin compounds which may be considered for such tin coupling are, for example, RSnCl3, (R)2SnCl2, (R)3Sn Cl, R2Sn(OR)3 and Sn(OR)4 wherein R is an aliphatic, cycloaliphatic, or aromatic hydrocarbon group, although SnCl4 (tin tetrachloride) is usually preferred.
For said functionalized conjugated diene-based elastomer, said functional groups may be positioned as individual groups (e.g. pendent groups) along the elastomer chain in a randomly spaced manner and/or in blocks of a plurality of said functional groups which may be generally exclusive of the terminal ends of the elastomer. Alternatively, at least one of said functional groups may be positioned at a terminal end of the elastomer.
The said first category of functional groups for said functionalized conjugated diene-based elastomer is intended to include groups which provide an adsorptive interaction with the precipitated silica aggregates. In particular, said first category of functional groups are considered herein as being significant in a sense of providing a degree of basicity and/or polarity to the conjugated diene-based elastomer to, in general, promote an adsorptive interaction with the typically relatively acidic and polar nature of the said precipitated silica aggregates to, in turn promote a separation of said precipitated silica aggregates and thereby retard their agglomeration within the elastomer host.
The said second category of functional groups for said functionalized conjugated diene-based elastomer is intended to include groups which form chemical bonds to the hydroxyl groups (e.g. silanol groups) of the precipitated silica aggregates. In particular, said second category of functional groups are considered herein as being significant by providing covalent bonding to the hydroxyl groups (e.g. silanol groups) on the surface of the said precipitated silica aggregates (particles), serving to both retard their agglomeration within the elastomer host and, in addition, to promote an improvement in various physical properties of the resulting vulcanized rubber composition.
For said first category of said functional groups, an example of an amine functionalized conjugated diene-based elastomer may be, for example, an amine functionalized styrene/conjugated diene copolymer such as, for example, a styrene/butadiene copolymer which contains from about 5 to about 40 weight percent bound styrene based upon the styrene/butadiene copolymer.
In practice, such amine functionalized styrene/conjugated diene copolymer may alternatively be, for example, an amine functionalized styrene/isoprene/butadiene terpolymer which contains from about 10 to about 30 weight percent (units derived from) styrene, about 10 to about 70 weight percent (units derived from) isoprene and about 10 to about 70 weight percent (units derived from) butadiene based upon the styrene/isoprene/butadiene terpolymer.
In practice, such amine functionalized styrene/conjugated diene copolymer elastomer and/or said additional conjugated diene-based elastomer may be tin coupled to provide an elastomer of significantly increased molecular weight and correspondingly increased Mooney (ML 1+4) viscosity.
Such amine functionalized styrene/conjugated diene copolymer elastomer may be provided as having at least one terminal amine group and/or as having pendant amine groups which are distributed along the copolymer itself.
For example, the amine groups might be introduced (positioned) along the copolymer chain by first introducing an amine group onto a monomer used in the formation of the copolymer. For example, the styrene monomer might be modified with an amine group. Further, and for example, divinylbenzene might be modified with an amine group and a very small amount of the modified divinylbenzene introduced into the styrene/conjugated diene copolymerization reaction.
For example, the amine groups might be introduced (positioned) as one or more terminal amine groups at an end of the copolymer chain by using an amine-modified polymerization initiator for the styrene/conjugated diene copolymerization reaction or by adding a chain terminating agent to the copolymerization reaction after a suitable copolymer has been formed. A chain terminating agent may be, for example, a pyrrolidine based material.
The following exemplary general formulas are provided as examples of various amine group substituents on the copolymer and are not intended to be limiting for this invention. In general, it is envisioned that the diene-based elastomer is attached to the amine group by one of the carbon atoms (a carbon atom included in an “R” group of the amine group). Alternatively, the elastomer (e.g. a butadiene moiety of the copolymer) can be attached directly to the nitrogen of the amine group.
For example, the functionalized conjugated diene-based elastomer may be a conjugated diene-based elastomer functionalized with at least one amine group of the general formula (II):
wherein x is a value of from 0 through 2, and R is selected from saturated straight chain alkyl radicals and saturated branched alkyl radicals which contain from 1 through 20 carbon atoms, alternately from 1 through 12 carbon atoms, where preferably at least one saturated alkyl radical contains from 1 through 6 carbon atoms; and from aryl radicals and substituted aryl radicals which contain from 6 to 30, alternately from 6 to 18, carbon atoms.
Such aryl amine groups (including alkaryl and aralkyl amine groups), may be, for example, of the general formulas (III-A and III-B), although such general formulas are not intended to be limiting:
wherein x is a value of from 0 to 2, R is selected from said saturated straight chain and said saturated branched alkyl radicals having from 1 through 20 carbon atoms, alternately from 1 through 6 carbon atoms, wherein at least one R preferably contains from 1 through 6 carbon atoms. For Formula (III-B), the nitrogen atom of the amine can be positioned on either the meta or para positions of the aromatic ring relative to the position of the R radical.
For the above general formulas (II), (III-A) and (III-B), representative of said saturated straight chain alkyl radicals are, for example, methyl, ethyl, n-propyl, n-butyl, n-pentyl and n-hexyl radicals. Representative of said saturated branched alkyl radicals are, for example isobutyl, isopropyl, isopentyl and isohexyl radicals.
In practice, said amine groups for said first category of functional groups may also be heterocyclic amine groups, for example, selected from pyridine, pyrrolidine, piperidine, hexamethyleneimine and indole based groups. Such heterocyclic amine groups may be, for example, of the general formulas IV-A (pyridines), IV-B (pyrrolidines), IV-C (piperidines), IV-D (hexamethyleneimines) and IV-E (indoles) although such general formulas are not intended to be limiting:
wherein, for said general formulas (IV-A), (IV-B), (IV-C), (IV-D) and (IV-E), x is a value of from zero through 2, alternately and preferably 1, and wherein R2 is a saturated alkyl radical containing from 1 through 6, alternately and usually preferably from 1 through 3, carbon atoms. The R2 radicals are appropriately positioned on the associated ring. For example, for formula IV-A, a single R2 radical may be positioned in an ortho position to the nitrogen atom. For example, for formula IV-B, a single R2 radical may be positioned in a meta position to the nitrogen atom. For example, for formula IV-C, a single R2 radical may be positioned on the six member ring two carbon atoms away from the five member ring.
Representative of said saturated alkyl radicals for R2 are, for example, methyl, ethyl and n-propyl radicals.
For example, an amine functionalized styrene/conjugated diene copolymer elastomer having at least one terminal amine group may be provided by copolymerizing styrene and at least one of 1,3-butadiene and isoprene monomers in an organic solvent solution with a non-cyclic amine initiator such as 3-(N,N-dimethylamine)-1-propyl lithium as Al-200™ from the FMC company. It is contemplated that such initiator may be represented by the general formula (V) to impart at least one terminal tertiary amine group, as a tertiary amine group of the aforesaid general formula (II) in that two of the R substituents are methyl groups and one of the R substituents is an n-propyl group with the copolymer being attached to the carbon atom of the n-propyl group occupied by the lithium of the initiator, namely
In one aspect, the above amine based initiator may also be provided as being “chain extended” by containing a minor amount of an isoprene moiety in its chain which apparently may provide the resultant terminal amine functionalized styrene/conjugated diene copolymer elastomer of improved processability by exhibiting a reduced Mooney viscosity of the unvulcanized elastomer. Exemplary of such initiator is understood to be Al-200 CE™ from the FMC Company.
Alternately, an amine functionalized styrene/conjugated diene copolymer elastomer having at least one terminal amine group may be provided by copolymerizing styrene with 1,3-butadiene and/or isoprene monomers in an organic solvent solution with a pyrrolidine (cyclic amine) based initiator such as 3-pyrrolidino-1-propyl lithium from the FMC Company.
In a further aspect, the amine groups may be formed as pendent and/or terminal groups along the elastomer chain by, for example, pre-reacting divinyl benzene with a suitable amine to form a modified divinyl benzene which contains the amine substituent. A small amount (e.g. one to two percent of the total styrene and 1,3-butadiene monomers) of the modified divinyl benzene is introduced into the polymerization of the monomers (e.g. styrene with at least one of 1,3-butadiene and isoprene monomers) at a desirable stage of the copolymerization process in an organic solvent solution.
Alternatively, for preparation of an amine functionalized styrene/butadiene elastomer, the styrene monomer itself may be modified with, for example, a pyrrolidone and the modified styrene is copolymerized with at least one of 1,3-butadiene and isoprene monomer(s) in an organic solvent solution. It is envisioned that pendant amine groups are thereby provided on the resulting styrene/conjugated diene copolymer elastomer.
Alternatively, a vinyl pyrrolidone may be introduced during the copolymerization of the styrene with at least one of 1,3-butadiene and isoprene monomers to effect pendant amine groups from the resultant styrene/butadiene copolymer elastomer.
For said second category of functional groups for said functional diene-based elastomer which are capable of forming covalent bonds to precipitated silica, examples include silanol, alkoxysilane, hydrogenated benzene, ketone, alcohol, aldehyde, ester and epoxy groups.
For example, second category functional group may be an alcohol group derived from 4,4′-bis(dimethylamino)-benzophenone, 4,4′ bis(ethylamino)-benzophenone, 4,4′bis(dibutylamine)-benzophenone, 4,4′diaminobenzophenone or 4-dimethylaminobenzophenone
Said functionalized diene-based elastomer may also include multiple categories and/or types of said first category and said second category functional groups in the same elastomer. Representative examples include polymers containing both epoxy and amine functional groups (for example see patent publication US2003/0199669 A1), containing both amine and alkoxysilane functional groups (for example see patent publication WO/03029299) and containing both alcohol groups derived from diethylamino benzophone and tin functional groups (for example see patent publication U.S. Pat. No. 4,550,142).
In further accordance with the invention, a tire is provided with a rubber tread wherein the running surface of said tread is configured with a plurality of longitudinal, circumferential rubber zones wherein the running surface of at least one of said tread zones is a circumferential longitudinal specialized tread strip wherein said specialized tread strip is comprised of the silica reinforced tread rubber composition of this invention which contains a combination of at least one of said functionalized conjugated diene-based elastomers and said blocked alkoxyorganomercaptosilane coupling agent for said silica.
For example, a tire is provided wherein the said tread running surface is a circumferential longitudinal tread zone (e.g. tread strip) in combination with at least one additional circumferential longitudinal tread zone (e.g. tread strip), wherein:
(A) said additional circumferential longitudinal tread zone is a rubber composition comprised of a non-functionalized rubber selected from at least one of polymers of at least one of isoprene and 1,3-butadiene and copolymers of styrene and at least one of isoprene and 1,3-butadiene at least, or
(B) said additional circumferential longitudinal tread zone is a rubber composition comprised of at least one of said functionalized elastomers of this invention.
Therefore, in one aspect of this invention, said running surface of said tire is comprised of a plurality of parallelly aligned longitudinal, circumferential rubber tread zones wherein at least one of said tread rubber zones is comprised of the functionalized conjugated diene-based elastomer composition of this invention and at least one of said tread rubber zones is exclusive of (does not contain) said functionalized conjugated diene-based elastomer composition of this invention.
Said tread zone of functionalized conjugated diene-based elastomer rubber composition of this invention may be positioned on the centerline of the tread running surface of may be spaced apart from the centerline of the tread running surface.
It is considered herein that such tire with a running surface comprised of said plurality of circumferential tread zones is significant in that such combination of varied rubber compositions presented in plurality of tread zones enables a simultaneous optimization across the tread running surface of desirable tire tread properties including, for example, acceptable road traction in wet, dry and snow conditions, acceptable resistance to tread wear and promotion of acceptable reduced tire rolling resistance, depending somewhat upon the desired tire tread properties and vehicular demands.
It is to be appreciated that the tire of this invention may be prepared by a process which comprises the steps of:
(A) mixing a mixture comprised of at least one of said functionalized elastomers, optionally including at least one of said additional diene-based elastomers, and said reinforcing filler in at least one sequential mixing step in an internal rubber mixer to a temperature in a range of from about 140° C. to about 175° C. in the absence of free addition of sulfur and organic sulfur vulcanization accelerator;
(B) thereafter, (which may be included in the above or subsequent mixing step), mixing therewith said blocked alkoxyorganomercaptosilane, which contains said blocking agent for the mercapto group thereof, to a temperature in a range of from about 140° C. to about 175° C.;
(C) thereafter, in a subsequent mixing step, mixing therewith free sulfur, at least one organic sulfur vulcanization accelerator and at least one unblocking agent to a temperature in a range of from about 95° C. to about 120° C.;
wherein said rubber mixtures are allowed to cool to a temperature below 40° C. between said mixing steps;
(D) shaping the resulting mixture of step (C) to form a shaped unvulcanized rubber tire tread strip and building a tire which contains said unvulcanized tread strip to form a tire assembly thereof followed by sulfur vulcanizing said tire assembly in a in a suitable mold at an elevated temperature in a range of from 125° C. to about 180° C. to form the tire of this invention;
wherein the chemical activity of the mercapto group of said blocked alkoxyorganomercaptosilane is substantially blocked from interacting with said diene-based elastomer until said unblocking agent is mixed therewith and allowed to subsequently unblock said blocked mercapto group of said blocked alkoxyorganomercaptosilane substantially at said elevated vulcanization temperature and thereby enable the unblocked mercapto group to interact with said diene-based elastomer) substantially subsequent to said mixing thereof.
As hereinbefore discussed if an unblocking agent should be desired, exemplary thereof is, for example, N,N′-diphenylguanidine and N,N′-di-ortho-tolylguanidine.
It is to be appreciated that the said unblocking agent is a material capable of unblocking the blocked alkoxyorganomercaptosilane to enable the mercapto group, or moiety, of the alkoxyorganomercaptosilane to interact with the diene based elastomer(s). It is to be appreciated that choice of the unblocking agent will depend upon the blocking group, or moiety, used to block the chemical activity of the alkoxyorganomercaptosilane itself insofar as interacting with a diene-based elastomer is concerned, which would be readily understood by one having skill in such art.
For a further discussion relating to said blocked alkoxyorganomercaptosilane coupling agent, representative of usually preferred blocked alkoxyorganomercaptosilanes are those where R1 has a primary carbon attached to the carbonyl as an alkyl group which contains from 2 to 12, preferably from 6 through 8, carbon atoms; and where G is a divalent hydrocarbon radical.
Representative examples of G are, for example, —(CH2)n— radicals where n is a value of from 1 to 12, diethylene cyclohexane, 1,2,4-triethylene cyclohexane, and diethylene benzene radicals. In practice, it is preferred that the sum of the carbon atoms within the G and Y groups is from 4 to 24, more preferably from 6 to 18. It is considered herein that such amount of carbon atoms in the blocked mercaptoalkoxysilane may aid in facilitating the dispersion of the composite of pre-reacted silica into the diene-based elastomer(s), whereby it is envisioned that a balance of physical of properties in the cured reinforced elastomer(s) is improved.
In practice, the R group of the blocked alkoxyorganomercaptosilane is preferably selected from hydrogen atom and saturated alkyl groups having from 1 through 18 carbon atoms wherein, alternately said R groups are methyl groups or wherein, alternately one or two of said R groups is a methyl group and the remainder of said R groups are saturated alkyl groups having from 3 through 18 carbon atoms.
Representative examples of X are, for example, methoxy, ethoxy, isobutoxy, propoxy, isopropoxy, acetoxy and oximato groups. Preferably, X is selected from methoxy, acetoxy and ethoxy groups. In practice, at least one X must be reactive (i.e., hydrolyzable).
In practice, for a usually preferred blocked mercaptoalkoxysilanes, Y is phenyl, cyclohexyl, or straight chain or substituted straight chain alkyl radical having from 3 to 18 carbon atoms. For a more preferred blocked alkoxyorganomercaptosilane, Y is a straight chain or substituted strait chain alkyl radical having from 6 to 18 carbon atoms.
An exemplary amount of the unblocking agent may be, for example, about 0.1 to about 5 phr; alternately in a range of from 0.5 to 3 phr, depending somewhat upon the nature of the blocked alkoxyorganomercaptosilane, the unblocking agent and the mercapto coupling activity desired with the respective specialized elastomer.
An unblocking agent, if used, is typically mixed with the rubber mixture subsequent to the preparation of the composite of amorphous precipitated silica and may be added together with the sulfur curative in the final curative addition mixing stage.
As hereinbefore mentioned, examples of unblocking agents include, for example, the hereinbefore referenced N,N′-diphenylguanidine, N,N′-di-ortho-tolylguanidine as well as, for example, hexamethylenetetramine and 4,4′-diaminodiphenylmethane.
Thus, when it is desired to unblock the blocked mercaptoalkoxysilane to enable the mercapto group (moiety) to interact with the specialized elastomer(s) to thereby couple the amorphous precipitated silica to the elastomer(s) it is seen that various unblocking agents may optionally be used, depending somewhat upon the blocking moiety, or agent, used to block the chemical activity of the mercapto group of the blocked mercaptoalkoxysilane.
Representative examples of various alkoxyorganomercaptosilanes prior to the blocking thereof are, for example, triethoxy mercaptopropyl silane, trimethoxy mercaptopropyl silane, methyl dimethoxy mercaptopropyl silane, methyl diethoxy mercaptopropyl silane, dimethyl methoxy mercaptopropyl silane, triethoxy mercaptoethyl silane, and tripropoxy mercaptopropyl silane.
Representative examples of various blocked alkoxyorganomercaptosilanes may be, for example, 2-triethoxysilyl-1-ethyl thioacetate; 2-trimethoxysilyl-1-ethyl thioacetate; 2-(methyldimethoxysilyl)-1-ethyl thioacetate; 3-trimethoxysilyl-1-propyl thioacetate; triethoxysilylmethyl thioacetate; trimethoxysilylmethyl thioacetate; triisopropoxysilylmethyl thioacetate; methyldiethoxysilylmethyl thioacetate; methyldimethoxysilylmethyl thioacetate; methyldiisopropoxysilylmethyl thioacetate; dimethylethoxysilylmethyl thioacetate; dimethylmethoxysilylmethyl thioacetate; dimethylisopropoxysilylmethyl thioacetate; 2-triisopropoxysilyl-1-ethyl thioacetate; 2-(methyldiethoxysilyl)-1-ethyl thioacetate; 2-(methyldiisopropoxysilyl)-1-ethyl thioacetate; 2-(dimethylethoxysilyl)-1-ethyl thioacetate; 2-(dimethylmethoxysilyl)-1-ethyl thioacetate; 2-(dimethylisopropoxysilyl)-1-ethyl thioacetate; 3-triethoxysilyl-1-propyl thioacetate; 3-triisopropoxysilyl-1-propyl thioacetate; 3-methyldiethoxysilyl-1-propyl thioacetate; 3-methyldimethoxysilyl-1-propyl thioacetate; 3-methyldi isopropoxysilyl-1-propyl thioacetate; 1-(2-triethoxysilyl-1-ethyl)-4-thioacetylcyclohexane; 1-(2-triethoxysilyl-1-ethyl)-3-thioacetylcyclohexane; 2-triethoxysilyl-5-thioacetylnorbornene; 2-triethoxysilyl-4-thioacetyinorbornene; 2-(2-triethoxysilyl-1-ethyl)-5-thioacetyinorbornene; 2-(2-triethoxysilyl-1-ethyl)-4-thioacetylnorbornene; 1-(1-oxo-2-thia-5-triethoxysilylpenyl)benzoic acid; 6-triethoxysilyl-1-hexyl thioacetate; 1-triethoxysilyl-5-hexyl thioacetate; 8-triethoxysilyl-1-octyl thioacetate; 1-triethoxysilyl-7-octyl thioacetate; 6-triethoxysilyl-1-hexyl thioacetate; 1-triethoxysilyl-5-octyl thioacetate; 8-triniethoxysilyl-1-octyl thioacetate; 1-trimethoxysilyl-7-octyl thioacetate; 10-triethoxysilyl-1-decyl thioacetate; 1-triethoxysilyl-9-decyl thioacetate; 1-triethoxysilyl-2-butyl thioacetate; 1-triethoxysilyl-3-butyl thioacetate; 1-triethoxysilyl-3-methyl-2-butyl thioacetate; 1-triethoxysilyl-3-methyl-3-butyl thioacetate; 3-trimethoxysilyl-1-propyl thiooctoate; 3-triethoxysilyl-1-propyl thiopalmitate; 3-triethoxysilyl-1-propyl thiooctoate; 3-triethoxysilyl-1-propyl thiobenzoate; 3-triethoxysilyl-1-propyl thio-2-ethylhexanoate; 3-methyldiacetoxysilyl-1-propyl thioacetate; 3-triacetoxysilyl-1-propyl thioacetate; 2-methyldiacetoxysilyl-1-ethyl thioacetate; 2-triacetoxysilyl-1-ethyl thioacetate; 1-methyldiacetoxysilyl-1-ethyl thioacetate; 1-triacetoxysilyl-1-ethyl thioacetate; 3-ethoxydidodecyloxy-1-propyl thioacetate; 3-ethoxyditetradecyloxy-1-propyl thioacetate; 3-ethoxydidodecyloxy-1-propyl-thiooctoate and 3-ethoxyditetradecyloxy-1-propyl-thiooctoate.
Various methods of preparation of various blocked alkoxyorganomercaptosilanes may be found, for example, in the aforesaid PCT/US98/17391 and U.S. Pat. No. 3,692,812 patent publications as well as in various literature publications such as, for example, in Gornowicz, G., “Preparation of Silylalkanethiols”, J. Org. Chem., Volume 33, No. 7, July, 1968; Vorkonov, M. G., et al., Trialkoxysilylalkanethiols and Bis(trialkoxysilylakyl)sulfides, Izvestiya Akademii Nauk SSSR and Seriya Khimicheskeya, No. 8, Pages 1849 through 1851, August 1977.
Various commercially available synthetic amorphous silica rubber reinforcement fillers, particularly precipitated silicas, may be used in the practice of this invention. Such silicas, typically in a form of aggregates thereof, are sometimes referred to in a sense of their BET (nitrogen surface area) and CTAB or DBP values as is well known to those having skill in such art. Representative of such silicas, for example, only and without limitation, are silicas available from PPG Industries under the Hi-Sil trademark with designations 210, 243, etc; silicas available from Rhodia, with designations of Zeosil 1165 MP and Zeosil 165GR, silicas available from Degussa AG with designations, for example, VN2 and VN3, and silicas available from Huber such as, for example, Zeopol 8745 and Zeopol 8715.
It is readily understood by those having skill in the art that the rubber composition of the tread rubber would be compounded by methods generally known in the rubber compounding art, such as mixing the various sulfur-vulcanizable constituent rubbers with various commonly used additive materials such as, for example, curing aids, such as sulfur, activators, retarders and accelerators, processing additives, such as oils, resins including tackifying resins and plasticizers, fillers, pigments, fatty acid, zinc oxide, waxes, antioxidants and antiozonants, peptizing agents and reinforcing materials as the hereinbefore referred to synthetic silica aggregates and rubber reinforcing carbon black.
The presence and relative amounts of the additives are not considered to be an aspect of the present invention, unless otherwise indicated.
The tires can be built, shaped, molded and cured by various methods which will be readily apparent to those having skill in such art.
While certain representative embodiments and details have been shown for the purpose of illustrating the invention, it will be apparent to those skilled in this art that various changes and modifications may be made therein without departing from the spirit or scope of the invention.
