CA2242310A1

CA2242310A1 - Diene polymers and copolymers incorporating partial coupling and terminals formed from hydrocarboxysilane compounds

Info

Publication number: CA2242310A1
Application number: CA002242310A
Authority: CA
Inventors: Daniel F. Graves; Sunil B. Sarkar; David F. Lawson; Hideo Takeichi
Original assignee: Bridgestone Corp
Current assignee: Bridgestone Corp
Priority date: 1997-07-11
Filing date: 1998-07-06
Publication date: 1999-01-11
Also published as: DE69818158T2; DE69818158D1; US6008295A; ES2205335T3; EP0890580B1; JPH11228647A; EP0890580A1

Abstract

Diene polymers or copolymers having improved balance between raw polymer viscosity and mixed compound viscosity, useful in tire tread compositions having highly balanced wet traction, rolling resistance, and traction in ice and snow, and fracture properties in the cured and white carbon reinforced states are provided. These diene polymers or copolymers comprise a mixture of diene polymer or copolymer chains containing carbon-tin bonds in the main polymer or copolymer chains and diene polymer or copolymer chains containing terminals derived from hydrocarboxysilane compounds.
The diene polymer or copolymers are prepared by first coupling a portion of the living diene polymer or copolymer chains obtained by anionic polymerization using a tin polyhalide coupling agent and then terminating the remaining living diene polymer or copolymer chains using hydrocarboxysilane compounds. The resultant diene polymers or copolymers have improved balance between raw polymer viscosity and mixed compound viscosity when compounded with silica and/or carbon black and cured compositions are useful in tire tread having highly balanced wet traction, rolling resistance, and traction in ice and snow. The polymers can be utilized to form elastomer compositions for tire treads having balanced properties of reduced rolling resistance and wet traction and handling or balanced properties of wet traction and handling and traction in snow and ice.

Description

FIELD OF THE INVENTION

2 The present invention relates to a polymer and a composition using said polymer.

3 More particularly, the present invention relates to a novel functionalized polymer having 4 excellent fracture properties, good abrasion resistance, excellent processability and a novel elastomeric composition for a tire tread using the functionalized polymer wherein the tire 6 tread formed from the composition displays an highly balanced wet traction, rolling 7 resistance ice and snow traction, and fracture property like wear performance.

9 As tires for higher performance are being developed, a rubber having superior fracture properties, good abrasion resistance and low hysteresis loss (low rolling resistance) is desired 11 as the rubber for the tire tread for such tires.
12 For decreasing the hysteresis loss, cis-1,4-polybutadiene rubber and the like are used.
13 However, the polybutadiene rubber and the like do not have good fracture properties even 14 though they have good abrasion resistance. As a rubber having a remarkably lower hysteresis loss, a solution polymerized butadiene-styrene rubber having the tin-carbon bond in the 16 molecular chain has been developed. However, this rubber does not always have a good 17 balance between wet grip and low rolling resistance.
18 An elastomeric composition for a tread in which carbon black alone is used as the 19 filler for the rubber described above can realize the desired balance between various properties and performances to some degree. However, simultaneous improvement of wet 21 grip and low rolling resistance to a higher degree has come to be required more urgently in 22 recent years and it is difficult for the rubber described above to satisfy this requirement. In 23 order to solve this problem, there have been disclosed elastomeric compositions in which white carbon such as silica is used alone or in combination with carbon black as the filler.
2 The use of silica in tire tread compositions sometimes improves the balance between wet 3 traction and traction in ice and snow. However, it has been known that diene polymers have 4 low affinity with white carbon such as silica and it is difficult to obtain a homogeneously 5 dispersed rubber composition by milling. To improve this drawback, a large amount of an 6 expensive silane coupling agent is mixed together in many cases. However, since the use of 7 these silane coupling agents in a rubber formulation generates a substantial amount of ethanol 8 in a Banbury mixer, the coupled rubbery mixture may contain undesirable large bubbles that 9 may form blisters or surface defects in the resultant formed articles. Silane coupling agent 10 which is widely used in the rubber industry for this purpose contains free sulfur groups which 11 are undesirable if present in a rubber formulation processed at high mixing temperatures 12 because "scorching" of the rubber may occur. Scorching reduces the processability of the 13 rubber or renders the rubber unusable.

14 In order to overcome many of these deficiencies the use of an elastomer having a 15 functionality that interacts with silica was proposed. An example of such elastomeric 16 composition is an elastomeric composition cont~ining a polymer modified with an 17 alkoxysilane compound at the end and a silica filler, as displayed in Japanese Patent 18 Publication Showa 52(1977)-5071, Japanese Patent Application Laid-Open Nos. Showa 19 56(1981)-104906, Showa 62(1987)-50346 and Showa 62(1987)-227908. With these 20 technologies, the physical properties of tires cont~ining the silane modified rubbers, silica and 21 other ingredients could be improved while reducing the necessary amount of the expensive 22 additive Si-69. However, due to the reaction occurring between the silica filler and the 23 hydrocarboxysilanes functionality of the polymers, Mooney viscosities of the resultant compounds were usually too high, thereby creating problems in mixing, in roll milling and in 2 extruding processes. A countermeasure to the high Mooney viscosity was to reduce the 3 molecular weight of the base diene polymer, however this solution created additional 4 problems at the synthetic rubber plant where polymers are made on an industrial scale. These polymers could not be processed by drying to a final rubber bale because of the low 6 molecular weight (Gum Mooney) of the hydrocarboxysilane terrnin~ted polymers. Also the 7 raw, low molecular weight diene polymers were susceptible to "cold flow"during storage.

Thus, the object of the current invention is to provide a polymer composition having a 11 workable molecular weight at synthesis in the polymer plant (e.g. no "hot flow" and "cold 12 flow"), good processability during mixing and the extrusion (tubing) process at the tire plant, 13 satisfying various required properties with a good balance and which is advantageous for 14 practical use.
The present invention displays diene polymers or copolymers formed from a lllixl~e 16 of:
17 (a) from about 10 to about 70 percent by weight of a diene polymer or copolymer of a diene 18 monomer and a vinyl aromatic hydrocarbon monomer cont~ining carbon-tin bonds in the 19 main polymer or copolymer chain, and (b) from about 90 to about 30 percent by weight of a diene polymer or copolymer of a diene 21 monomer and a vinyl aromatic hydrocarbon monomer cont~ining termin~l~, formed by 22 reacting living diene polymer or copolymer chains having organoalkali or organoalkaline 23 earth metal terminals with a hydrocarboxysilane compound, such as an alkoxysilane compound, aryloxysilane compound and aralkyloxysilane compound or mixtures thereof.
2 The diene polymers or copolymers are prepared by a method referred to as primary 3 partial coupling which involves first coupling a portion of the living diene polymer or 4 copolymer chains obtained by anionic polymerization with a tin halide coupling agent and then tennin:~ting the rem~ining living polymer or copolymer chains with a 6 hydrocarboxysilane compound, such as a alkoxysilane compound, aryloxysilane compound 7 and/or aralkyloxysilane compound.
8 Elastomer compositions of the invention may contain: (a) from 20 to 100 percent by 9 weight of said diene polymers or copolymers and (b) from 0 to 80 percent by weight of a rubber selected from the group consisting of natural rubber, polybutadiene rubber, 11 styrene-butadiene rubber and mixtures thereof.
12 Accordingly, an object of the present invention is to provide a novel functionalized 13 polymer having improved balance between raw polymer viscosity and mixed compound 14 viscosity, useful in tire tread compositions having highly balanced wet traction, rolling resistance, traction in ice and snow, and fracture properties in the cured and white carbon 16 reinforced states. To this end, the functionalized polymer of the present invention comprises a 17 diene-type polymer having a portion of the diene-type polymer tin-coupled and having a 18 portion of the diene-type polymer having terminal hydrocarboxysilane groups.19 The elastomeric composition of the present invention comprises a rubber material cont~ining a functionalized polymer in an amount of 10 or more parts by weight in 100 parts 21 by weight of the rubber material, and a filler of 10 to 100 parts by weight based on 100 parts 22 by weight of the rubber material, wherein the filler contains a white carbon, and the 23 functionalized polymer comprises a diene-type polymer having a portion of the diene-type polymer tin-coupled and having a portion of the diene-type polymer having a 2 hydrocarboxysilane group, such as an alkoxysilane group, an aryloxysilane group, or an 3 aralkyloxysilane group.

FIG. 1 is a graph showing the GPC curve which illustrates the molecular weight 6 distribution of the polymer of Example 1 before coupling or adding silane functionality.
7 FIG. 2 is a graph showing the GPC curve which illustrates the molecular weight 8 distribution of the polymer of Example 1 after SnCl4 coupling.
9 FIG. 3 is a graph showing the GPC curve which illustrates the molecular weight distribution of the polymer of Example 1 after sequentially coupling with SnCl4 and then 11 adding silane functionality by reaction with tetraethoxysilane(TEOS).
12 FIG. 4 is a graph showing the GPC curve which illustrates the molecular weight 13 distribution of the polymer of Example 5 after contemporaneous coupling with SnCl4 and 14 adding silane functionality by reaction with tetraethoxysilane(TEOS).
FIG. 5 is a graph showing the GPC curve which illustrates the molecular weight 16 distribution of the polymer of Example 4 after sequentially coupling with SnCl4 and then 17 adding silane functionality by reaction with tetraethoxysilane(TEOS).
18 FIG. 6 is a graph showing the GPC curve which illustrates the molecular weight 19 distribution of the SnCl4 coupled and silane functionalized polymer of Example 4 after treatment with HCl to breakdown the Sn-C coupling bonds.

DETAILED DESCRIPTION OF THE INVENTION
2 The term "living polymer" as employed throughout the specification and claims refers 3 to polymers which are prepared by anionic polymerization of a diene monomer or mixture of 4 a diene monomer and a vinyl aromatic hydrocarbon monomer using an initiator such as an organolithium compound. The resultant polymer contains active terminals (e.g. lithium 6 terminals) which can be subjected to coupling and/or lermin~ting reactions.
7 The term "hysteresis" as employed throughout the specification refers to the heat generating 8 properties of a vulcanized elastomer or rubber composition. An art recognized measurement 9 of the hysteresis of an elastomer composition is the tan delta value of the vulcanized composition. Low tan delta values at 50~ to 65~C. are indicative of low hysteresis and, 11 consequently, tires formed from such elastomer compositions have lower rolling resistance.
12 The diene polymers or copolymers of the invention are prepared by a process which 13 involves first preparing a living diene polymer or copolymer cont~inin~ active organoalkali or 14 organoalkaline earth metal termin~l~ by anionic polymerization of a conjugated diene monomer or mixture of a conjugated diene monomer and a vinyl aromatic hydrocarbon 16 monomer, coupling a portion of the living diene polymer or copolymer chains by reacting the 17 active terminals thereof with a tin polyhalide and then termin~ting the rem~inin~ portion of 18 the living diene polymer or copolymer chains by reacting the active terminals thereof with a 19 hydrocarboxysilane compound such as an alkoxysilane compound, aryloxysilane compound and/or aralkyloxysilane compound. It is preferable that greater than 50%, most preferably 80 21 to 100%, of the living ends of the rem~ining portion of the living diene polymer or copolymer 22 chains be terminated by reacting the active terminals thereof with a hydrocarboxysilane 23 compound. The rem~ining living ends may be termin~ted by methods well known to those skilled in the art such as with other known coupling agents, terminators, modifiers and 2 quenching techniques.
3 The living diene polymer is a polymer of a conjugated diene and the living diene 4 copolymer is a copolymer of a conjugated diene and a vinyl aromatic hydrocarbon. As the conjugated diene polymer, polybutadiene having excellent abrasion resistance is preferable.
6 As the conjugated diene/vinyl aromatic hydrocarbon copolymer, butadiene/styrene 7 copolymers having excellent abrasion resistance and aging resistance are preferable. The 8 microstructure of the butadiene part (cis-1,4, trans-1,4, and vinyl) in the diene-type polymer, 9 such as polybutadiene and butadiene/styrene copolymer, is not particularly limited, but can be in a range generally obtained by using an organolithium initiator. Composition of the 11 conjugated diene/vinyl aromatic hydrocarbon copolymer, such as butadiene/styrene 12 copolymer, is not particularly limited, but the ratio by weight ofthe conjugate diene unit to 13 the vinyl aromatic hydrocarbon unit is generally 99/1 to 20/80. The distribution of the units in 14 the copolymer may be a random distribution, a block distribution, or an intermediate distribution of these distributions. A random distribution and an intermediate distribution are 16 generally preferable.
17 Conjugated dienes which may be utilized in preparing the living polymers and 18 copolymers include 1, 3-butadiene, 2-methyl-1, 3-butadiene (isoprene), 2,3-dimethyl-1, 19 3-butadiene, 1,3 -pentadiene, 1 ,3-hexadiene and the like as well as mixtures thereof. The 20 preferred diene is 1,3-butadiene.
21 Vinyl aromatic hydrocarbons which may be utilized in plepa~ g the living 22 copolymers include styrene, vinyl toluene, alpha-methyl styrene, vinyl naphthalene, divinyl 23 benzene, vinyl pyridine and the like. The preferred vinyl aromatic hydrocarbon is styrene.

The living polymer can be prepared in a well known manner by polymerizing the 2 monomer or monomers in a hydrocarbon solvent in the presence of an anionic initiator. The 3 process of the present invention may be conducted in "batch", "semi-batch", "continuous" or 4 "dispersion" polymerization processes. The examples in this application were conducted in a 5 "batch" process, that is, with essentially one charge into a reactor until the reaction is 6 completed. In a "semi-batch" process, new monomer charges are periodically added by a 7 metering method into the polymerization reaction as the polymerization proceeds. In a 8 "continuous" process, initiator and monomer are continuously charged into a reactor. In a 9 "dispersion" process, polymerization is conducted in a state of suspension as described in U.S. Patent Nos. 5,331,035; 5,395,902; and 5,614,579.
11 In instances where it is desired to control the 1,2-microstructure of the diene polymer 12 or copolymer and to effect randomization of the copolymer, this can readily be accomplished 13 by including an applopl;ate polar modifier such as an ether or a tertiary amine in the 14 polymerization mixture.
Anionic initiators which may be utilized in the pl~pala~ion of the living polymers and 16 copolymers may be any of the organoalkali metal initiators known in the art to be useful for 17 the preparation of diene polymers and copolymers. The pl~fell~d initiators are organolithium 18 initiators, especially the alkyllithium initiators. Examples of the lithium compound used 19 include alkyllithiums, such as ethyllithium, propyl lithium, n-butyl lithium, sec-butyl lithium, 20 tert-butyl lithium, hexyl lithium, and the like; alkylene dilithium, such as 1,4-dilithiobutane, 21 and the like; phenyl lithium; stilbene dilithium; other hydrocarbon lithiums, such as reaction 22 products of butyl lithium and divinylbenzene, and the like; organometallic lithiums, such as 23 tributyltin lithium, and the like; and lithium amides, such as lithium diethylamide, lithium diisopropylamide, lithium piperidide, and the like. Among these lithium compounds, n-butyl 2 lithium and sec-butyl lithium are preferable. The lithium compound may be used singly or as 3 a mixture of two or more types. The lithium compound can be used in an amount in the range 4 of 0.2 to 30 mmol per 100 g of the monomer. The molecular weight of the polymer can easily be controlled by adjusting the concentration of the lithium compound.
6 It is also possible to employ as the anionic initiator an initiator formed by reacting a 7 function~li7ing agent with the above-described organolithium initiators. Thus, such initiators 8 can be formed by reacting a function~li7ing agent selected from the group con~i~ting of 9 substituted al~limines, ketimines and secondary amines with the organolithium compound.
For example, an anionic initiator of this type can be formed by reacting a substituted aldimine 11 such as dimethylamino benzylidene methylamine with n-butyl lithium. A number of initiators 12 of this type are described in our U.S. Pat. No. 5,066,729, the disclosure of which is 13 incorporated herein by reference.
14 Hydrocarbon solvents which may be employed in the preparation of the living polymers and copolymers include aromatic and aliphatic hydrocarbons in which the16 monomers, initiator and modifier are soluble. Suitable hydrocarbon solvents include hexane, 17 heptane, pentane, octane, cyclohexane, cycloheptane, cyclopentane, methyl cyclohexane, 18 benzene and toluene. The preferred hydrocarbon solvents are hexane and cyclohexane.
19 Polar modifiers which may be utilized to control the 1,2-microstructure content of the living diene polymers or copolymers and to effect randomization of the copolymers may be 21 any of those heretofore known in the diene polymer or copolymer art to be useful for that 22 purpose. Suitable polar modifiers include ethers such as tetrahydrofuran (THF), 23 tetrahydropyran, 1,4-dioxane, monoglycol methyl ether (monoglyme), diglycol methyl ether (diglyme), triglycol methyl ether (triglyme) and the oligomeric oxolanyl alkane compounds 2 described in U.S. Pat. No. 4,429,091 such as bis (2-oxolanyl) methane; 2,2-bis (2-oxolanyl) 3 propane; l,1-bis (2-oxolanyl) ethane; 2,2-bis (5-methyl-2-oxolanyl) propane and the like and 4 tertiary amine compounds such as triethyl amine, tripropyl amine, tributyl amine, N,N,N',N'-tetramethylethylene diamine (TMEDA), dipiperidino ethane, and the like. The 6 preferred polar modifiers are TMEDA and the oligomeric oxolanyl propanes.
7 The living copolymers of conjugated dienes and vinyl aromatic hydrocarbons utilized 8 to prepare copolymers of the present invention may have diene contents of from about 99 to 9 20 percent by weight and vinyl aromatic hydrocarbon contents of from about 1 to about 80 percent by weight with the plefc,l~ed copolymers having diene contents of from 95 to 50 11 percent by weight and vinyl aromatic hydrocarbon contents of from 5 to S0 percent by 12 weight.
13 The living polymers of conjugated dienes and copolymers of conjugated dienes and 14 vinyl aromatic hydrocarbons employed to prepare the polymers and copolymers ofthe l S invention may have 1,2-microstructure contents ranging from about 6 to about 80 percent 16 with the pler~lled polymers or copolymers having 1,2-microstructure contents of from l S to 17 65 percent. The preparation of diene polymers or copolymers having a particular 18 1,2-microstructure content is dependent on a number of factors including the specific 19 initiator, the type polar modifier, the modifier to initiator ratio and the polymerization temperature.
21 Illustrative methods of preparing diene polymers and copolymers having 22 l ,2-microstructure contents ranging from l S to 90 percent or more are described in numerous 23 patents and publications including U.S. Pat. Nos. 3,451,988 and 4,264,753; and the publication "Temperature and Concentration Effects on Polar-Modifier Alkyllithium 2 Polymerizations and Copolymeri_ation", Journal of Polymer Science, Part A-1, Vol. 10, 3 pages 1319-1334 (1972); the disclosures of which are incorporated herein by reference.
4 One of ordinary skill in the polymerization arts can, by utili7.ing the disclosures of the incorporated patents and publication, readily determine the type initiator, the type polar 6 modifier, the necessary modifier-initiator ratio and polymeri_ation conditions necessary to 7 obtain a living diene polymer or copolymer having the desired 1,2-microstructure content.
8 Aftter the conversion of charged mononmers to polymers reaches over 80 to 90%, a small 9 amount of a diene monomer, such as butadiene or isoprene, may be added to the polymerization system to convert the living polymer end into butadienyl-lithium (with the use 11 of butadiene) to facilitate the following reaction with a tin polyhalide while improving the 12 physical properties of the final product. This technique is described in U.S. Patent Nos.
13 4,383,085; 4,519,431; 4,526,934; and 4,603,722. The diene polymers or copolymers 14 cont~ining carbon-tin bonds in the main polymer or copolymer chains are prepared by coupling the desired amount of living diene polymer or copolymer chains by reacting the 16 alkali or ~ line earth metal t~rrnin~l~ thereof with a tin polyhalide having the formula 17 RaSnXb, wherein R is selected from the group consisting of alkyl, alkenyl, cyloalkyl and aryl 18 groups, X is a halogen atom, a is an integer of 0-2 and b is an integer of 2-4.
19 Illustrative examples of tin polyhalides which may be employed include methyltrichlorotin, dimethyldichlorotin, ethyltrichlorotin, diethyldichlorotin, 21 butyltrichlorotin, dibutyldichlorotin, octyltrichlorotin, dioctyldichlorotin, methyltribromotin, 22 dimethyldibromotin, octyltribromotin, tin tetrachloride, tin tetrabromide, tin tetraiodide, 23 cyclohexyltrichlorotin, phenyl trichlorotin, 1,2-bis (trichlorostannyl) ethane, 1,2-bis (methyldichlorostannyl) ethane, 1,4-bis (trichlorostannyl) butane, 1,4-bis 2 (methyldichlorostannyl) butane and the like. The preferred tin polyhalides are tin 3 tetrachloride and dibutyldichlorotin.
4 The coupling reaction is conducted by reacting the living polymers, preferably in solution in the hydrocarbon solvent in which they were prepared, with the tin polyhalide 6 coupling agent. The reaction can be carried out if desired by simply adding the coupling agent 7 per se to the polymer solution. However, it is generally preferred to add the coupling agent in 8 the form of a solution thereof in an applopliate solvent for ease of handling.
9 The amounts of coupling agent added to the living polymer are dependent upon the amounts of live organoalkali metal end groups (e.g. live lithium end groups) present in the 11 living polymer and the amount of coupled polymer desired in the finished polymer 12 composition. It should be noted that the number of moles of live alkali metal end groups in 13 the living polymer is presumed to be equivalent to the number of moles of alkali metal groups 14 present in the organoalkali metal initiator utilized to effect polymerization. In general, the amount of tin polyhalide coupling agent employed to react with the live alkali metal end 16 groups of the living polymer chains may range from about 0.1 to about 0.8 equivalents of tin 17 polyhalide, based on the number of halogen atoms in said tin polyhalide, per mole of living 18 polymer chains. However, preferred amounts of tin polyhalide range from 0.1- to 0.6 19 equivalents with 0.15 to 0.50 equivalents being especially preferred.
Temperatures employed in coupling the living polymer chains with the coupling agent 21 may vary considerably and are selected with the basic criteria of preserving the live alkali 22 metal end groups of the living polymer chains for reaction with the coupling agent and, 23 subsequently, the terrnin:~ting agent. Thus, the reaction temperatures may range from about 0~ C. to about 100~ C. with preferred temperatures ranging from 30~ C. to 100~ C. and 2 especially preferred temperatures ranging from 50~ C. to 80~ C. The reaction times may also 3 vary somewhat and are, in general, dependent upon reaction temperatures. Hence, the reaction 4 times may range from about 0.5 minutes to about 60 minutes with preferred reaction times ranging from 1 to 30 minutes.
6 The diene polymers or copolymers cont~inin~ terminals derived from a 7 hydrocarbyloxysilane compounds are prepared by reacting the r~m~inin~ living polymer or 8 copolymer chains, preferably in solution, with a tennin~ting agent such as a9 hydrocarbyloxysilane compound. Hydrocarboxysilane compounds which may be employed include alkoxysilane compound, aryloxysilane compound and/or aralkyloxysilane compound 11 used in the pl~l)al~lion of the functionalized polymer represented by the formula (1):
12 Si(R4)(4 y)(0R3)(y) (1) 13 wherein R3 and R4 in formula (1) represent a group selected from an aliphatic hydrocarbon 14 group, an alicyclic hydrocarbon group, or an aromatic hydrocarbon group, each having 20 or less, preferably 10 or less, carbon atoms, and y represents an integer of 1 to 4, and R4 may be 16 a halo group including chloro. Examples of the aliphatic hydrocarbon group include methyl 17 group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, octyl group, and the 18 like. Examples of the alicyclic hydrocarbon group include cyclopentyl group, cyclohexyl 19 group, cycloheptyl group, and the like. Examples of the aromatic hydrocarbon group include phenyl group, naphthyl group, biphenyl group, anthryl group, phenanthryl group, and the 21 like. R3 is preferably an aliphatic hydrocarbon group or an aromatic hydrocarbon group, each 22 having l O or less carbon atoms. R3 and R4 are each most preferably methyl group, ethyl 23 group, propyl group, or phenyl group. R4 is not present in the functionalized polymer when the number of oR3 bonded to silicon have some specified values [i.e., when y=4 in formula 2 (1)].
3 In formula (1), y represents an integer of 1 to 4. The functionalized polymer may be a 4 single compound having fixed values of y in formula (1 ) or a mixture of compounds having various values of y in formula (1).
6 The alkoxysilane compound, aryloxysilane compound and/or aralkyloxysilane 7 compound are not particularly limited and a substituted or unsubstituted tetraalkoxysilane 8 compound, an alkylalkoxysilane compound, an arylalkoxysilane compound, an 9 alkenylalkoxysilane compound, a halogenoalkoxysilane compound, or the like can be used. In the present description an alkoxy group, an aryloxy group, and an aralkyloxy group are those 11 in which the hydrocarbon group replacing the hydrogen atom of the hydroxyl group is an 12 aliphatic hydrocarbon group, an aromatic hydrocarbon group, and an aralkyl hydrocarbon 13 group, respectively.
14 Examples of the tetraalkoxysilane compound described above include tetramethoxysilane, tetraethoxysilane, tetra-n-propoxysilane, tetra-n-butoxysilane, 16 tetra(2-ethylhexanoxy)silane, tetraphenoxysilane, tetratoluyloxysilane, and the like.
17 Examples of the alkylalkoxysilane compound described above include 18 methyltrimethoxysilane, methyltriethoxysilane, methyltri-n-propoxysilane, 19 methyltri-n-butoxysilane, methyltriphenoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, ethyltri-n-propoxysilane, ethyltri-n-butoxysilane, ethyltriphenoxysilane, 21 dimethyldimethoxysilane, dimethyldiethoxysilane, dimethyldi-n-propoxysilane, 22 dimethyldi-n-butoxysilane, dimethyldiphenoxysilane, diethyldimethoxysilane,23 diphenyldimethoxysilane, 3-glycidoxypropyltrimethoxysilane (GPMOS), ~-methacryloxy propyl trimethoxysilane and the like.
2 Examples of the arylalkoxysilane compound described above include 3 phenyltrimethoxysilane, phenyltriethoxysilane, phenyltri-n-propoxysilane, 4 phenyltri-n-butoxysilane, phenyltriphenoxysilane, and the like.
Examples of the alkenylalkoxysilane compound described above include 6 vinyltrimethoxysilane, vinyltriethoxysilane, vinyltri-n-propoxysilane, vinyltri-n-butoxysilane, 7 vinyltriphenoxysilane, allyltrimethoxysilane, octenyltrimethoxysilane, 8 divinyldimethoxysilane, ~lylylllilllethoxysilane, and the like.
9 Examples of the halogenoalkoxysilane compound described above include trimethoxychlorosilane, triethoxychlorosilane, tri-n-propoxychlorosilane, 11 tri-n-butoxychlorosilane, triphenoxychlorosilane, dimethoxydichlorosilane, 12 diethoxydichlorosilane, di-n-propoxydichlorosilane, diphenoxydichlorosilane,13 methoxytrichlorosilane, ethoxytrichlorosilane, n-propoxytrichlorosilane, 14 phenoxytrichlorosilane, trimethoxyblolllosilane, triethoxybromosilane, tri-n-propoxybromosilane, triphenoxybromosilane, dimethoxydibromosilane, 16 diethoxydibromosilane, di-n-propoxydibromosilane, diphenoxydibromosilane, 17 methoxytribromosilane, ethoxytribromosilane, n-propoxytribromosilane, 18 phenoxytribromosilane, trimethoxyiodosilane, triethoxyiodosilane, tri-n-propoxyiodosilane 19 triphenoxyiodosilane, dimethoxydiiodosilane, di-n-propoxydiiodosilane, diphenoxydiiodosilane, methoxytriiodosilane, ethoxytriiodosilane, n-propoxytriiodosilane, 21 phenoxytriiodosilane, and the like.
22 Other useful silanes include bis(trimethoxysilane)-ether, Si-69 (Bis-( 3-23 {triethoxysilyl}- propyl)-tetrasulfide) and the like.

The reaction of the living polymer in solution with the terrnin:~ting agent can be 2 conducted if desired by simply adding the terrnin~ting agent per se to the polymer solution.
3 However, it is generally preferred to add the terrnin~ting agent in the form of a solution 4 thereof in an appropriate solvent for ease of handling. The terrnin~ting agent may be added simultaneously with the tin polyhalide coupling agent or after the tin polyhalide coupling 6 agent. The tçrrnin~ting agent should not be added prior to the addition of the Sn coupling 7 agent.
8 The amounts of tçnnin~ting agent added to the living polymer are dependent upon the 9 amounts of live organoalkali metal end groups (e.g. live lithium end groups) present in the living polymer and the amounts oftçrrnin~te~l polymer desired in the finished polymer 11 composition. It will be noted that the number of moles of live alkali metal end groups in the 12 living polymer is presumed to be equivalent to the number of moles of alkali metal groups 13 present in the organoalkali metal initiator utilized to effect polymerization assuming that the 14 hlll~ul;Lies in the system is low enough. In general, the amount of termin~tinp agent employed to react with the live alkali metal groups of the living polymer chains may range from about 16 0.3 to about 100 moles of said terrnin~ting agent per mole of living polymer chains. However, 17 the plefelled amounts range from 0.4 to 2.0 moles of such tçrrnin~ting agent per mole of 18 living polymer chains.
19 Temperatures employed in reacting the living polymer with the terrnin~ting agent may vary considerably and are selected with the basic criteria of preserving the live alkali metal 21 end groups ofthe living polymer for reaction with the terrnin~ting agents. Thus, the reaction 22 temperatures may range from about 0~ C. to about 100 ~ C. with the preferred temperatures 23 ranging from 30~C. to 100~C. and especially preferred temperatures ranging from 50~C. to 80'' C. The reaction times may also vary considerably and are, in general, dependent upon 2 reaction temperatures. Hence, the reaction times may range from about 15 minutes to about 3 24 hours.
4 After the terrnin~ting reaction is complete, it is desirable to neutralize the polymer cement to prevent the reaction between two or more functional ends of the polymer during 6 work-up. Neutralizing agents include acids such as 2-ethylhexanoic acid or benzoic chloride.
7 The resultant diene polymer or copolymer which contains a mixture of polymer 8 cont~ining carbon-tin bonds and polymer cont~qinin~ terminals derived from 9 hydrocarboxylsilane compounds may be recovered from the polymer solution and dried using conventional procedures. Thus, for example, the polymer mixture can be recovered from 11 solution by direct drum drying, extruder drying, air drying or by coagulation either by adding 12 a sufficient volume of a non-solvent liquid (e.g. an alcohol) for the polymer to the solution or, 13 alternatively, by adding the polymer solution to a sufficient volume of the non-solvent. It is 14 usually desirable in carrying out the coagulation procedure to include an a~ opliate antioxidant for the polymer in the non-solvent. The recovered polymer can then be dried 16 using a conventional polymer drying procedure such as drum drying, vacuum drying, 17 extruder drying, tunnel drying, oven drying and the like.
18 The diene polymers or copolymers of the invention may contain from about 10 to 19 about 80 percent by weight of polymer or copolymer containing carbon-tin bonds and correspondingly from about 90 to about 20 percent by weight of polymer or copolymer 21 containing terminals derived from hydrocarbonyloxylsilane compounds. However, the 22 preferred compositions are those containing from about 15 to about 50 percent by weight of 23 polymer or copolymer containing carbon-tin bonds and from about 50 to about 85 percent by weight of polymer or copolymer cont~ining terminals derived from hydrocarbonyloxylsilane 2 compounds.
3 It should be noted here that during the polymerization of the monomer(s) to prepare the living 4 diene polymer or copolymers a minor proportion of living ends may be terrnin~te~l with S hydrogen or by loss of lithium hydride particularly in instances where the polymerization is 6 conducted at high temperatures. Hence, the polymer compositions may contain minor 7 proportions of such terminated polymers in addition to the diene polymers or copolymers of 8 the invention.
9 As indicated, the elastomer compositions of the invention may contain (A) from 20 to 100 percent by weight of diene polymer or copolymer mixture consisting of diene polymer or 11 copolymer cont~ining carbon-tin bonds and diene polymer or copolymer cont~ining terminals 12 derived from hydrocarbonyloxylsilane compounds and (B) from 0 to 80 percent by weight of 13 a rubber selected from the group consisting of natural rubber, polyisoprene, polybutadiene 14 rubber, styrene-butadiene rubber or mixtures thereof. Such compositions can be prepared by compounding or mixing said diene polymer of copolymer composition component optionally 16 with the other rubber component along with white carbon like silica, carbon black and other 17 conventional rubber additives such as fillers, plasticizers, antioxidants, curing agents and the 18 like using standard rubber mixing equipment and procedures. Such elastomer compositions 19 when vulcanized using conventional rubber vulcanization conditions have highly balanced wet traction, rolling resistance, ice and snow traction, and fracture property like wear 2 1 performance.
22 Fillers are used in the elastomeric compositions of the present invention. White 23 carbon is the essential component of the filler. Examples of the white carbon used in the elastomeric composition of the present invention include wet silica (hydrated silicic acid), dry 2 silica (anhydrous silicic acid), calcium silicate, aluminum silicate, clay, talc, calcium 3 carbonate, basic magnesium carbonate, hydrated alumina, diatomaceous earth, barium sulfate, 4 mica, aluminum sulfate, titanium oxide, aluminum hydroxide, aluminum oxide and the like.
Among these white carbons, wet silica is preferable because it can highly balance wet 6 traction, rolling resistance, ice and snow traction, and fracture properties.
7 The content of the filler in the elastomeric composition is 10 to 150 parts by weight, 8 preferably 20 to 90 parts by weight, based on 100 parts by weight of the total elastomeric 9 rubbery material, that is the combination of the functionalized polymer and additional rubber if present. When the content is less than 10 parts by weight, the fracture properties are 11 insufficient. When the content is more than 150 parts by weight, processability is inferior.
12 The filler of the present invention may contain the white carbon alone. In this case, 13 the content of the white carbon in the elastomeric composltion is 10 to 150 parts by weight, 14 preferably 20 to 90 parts by weight, based on 100 parts by weight of the rubber material.
When the content is less than 10 parts by weight, the fracture properties are insufficient.
16 When the content is more than 150 parts by weight, processability is inferior.
17 The filler of the present invention may contain the white carbon and carbon black in 18 combination. The effect of the filler on the improvement of the physical properties is 19 remarkably enhanced by this combination. As the carbon black, FEF, SRF, HAF, ISAF, SAF, and the like, are used. Carbon blacks having an iodine adsorption number (IA) of 60 mg or 21 more per g, and a dibutyl phth~ te absorption number (DBP) of 80 ml or more per 100 g, are 22 preferably used. HAF, ISAF and SAF having superior abrasion resistance are particularly 23 preferable. The amount of the carbon black used is not particularly limited as long as it is within such a range that the effect of the white carbon is not adversely affected. From the 2 standpoints of the reinforcing property and processability, it is preferred that 0 to 100 parts by 3 weight of the carbon black and 0 to 150 parts by weight of the white carbon, each based on 4 100 parts by weight of the rubber material, are used as long as the content of the filler is within the range described above.
6 In the elastomeric composition of the present invention, the hydrocaboxysilane 7 tennin~1ing agent, such as Si-69, is used in the preparation of the elastomeric composition for 8 the purpose of further enhancing the reinforcement with the white carbon.
9 Examples of the vulc~ni7.ing agent include sulfur and the like. The amount of the vulç~ni7.ing agent used is 0.1 to 5 parts by weight, preferably 1 to 3 parts by weight, based on 1 1 100 parts by weight of the rubber material. When the amount is less than 0.1 parts by weight, 12 the fracture properties, abrasion resistance, and low hysteresis loss of the vulcanized rubber 13 are inferior. When the amount is more than 5 parts by weight, the rubber elasticity is lost.
14 Examples of the process oil which can be used in the elastomeric composition of the present invention include paraffinic process oils, naphthenic process oils, and aromatic 16 process oils. For applications in which tensile strength and abrasion resistance are important, 17 aromatic process oils are used. For applications in which hysteresis loss and low temperature 18 properties are important, naphthenic process oils and paraffinic process oils are used. The 19 amount of the process oil used is 0 to lO0 parts by weight based on 100 parts by weight of the rubber material. When the amount is more than 100 parts by weight, tensile strength and low 21 hysteresis loss of the vulcanized rubber deteriorate significantly.
22 Vulcanization accelerators used in the present invention are not particularly limited.
23 Examples of the vulcanization accelerator include thiazol vulcanization accelerators, such as M (2-mercaptobenzothiazol), DM (dibenzothiazyl disulfide), CZ
2 (N-cyclohexyl-2-benzothiazyl- sulfenamide) and the like; and guanidine vulcanization 3 accelerators, such as DPG (diphenylguanidine) and the like. The amount of the vulcanization 4 accelerator used is 0.1 to 5 parts by weight, preferably 0.2 to 3 parts by weight, based on 100 parts by weight of the rubber material.
6 In the elastomeric composition of the present invention, additives, such as 7 antioxidants, zinc oxide, stearic acid, antiozonants, and the like which are conventionally 8 used in the rubber industry may be l~tili7Pfl 9 The elastomeric composition of the present invention can be obtained by milling the components by using a milling apl)aldl~ls, such as a mill, an internal mixer, and the like. In 11 the mixing of the hydrocarboxysilane terminated polymer and the silica filler, it is important 12 to conduct the mixing for a sufficient time and at a high enough temperature to ensure the 13 compounding reaction of the silane functional end of the polymer with the silica. Actual 14 compounding tempeld~ules should be in the range of 140~to 190~C. After being molded and vulc~ni7P~ the elastomeric composition may be applied to tires, such as tire treads, 16 undertreads, carcasses, side walls, beads, and the like, as well as to other industrial rubbers, 17 such as antivibration rubbers, belts, hoses, Rubber Crawlers, shoes and the like. The 18 elastomeric composition is particularly preferably used as a rubber for tire treads.
19 To summarize the advantages of the present invention, the functionalized polymers and the compounded elastomeric compositions of the present invention exhibit good work-up 2 l processability at the synthetic rubber plant; low compound viscosity and good mixing, roll 22 mill, and extrusion processabilities at the tire plant; excellent fracture properties; abrasion 23 resistance; and low hysteresis loss (low rolling resistance and low fuel consumption) properties as a cured tire because the functionalized polymer and the elastomeric composition 2 have the structure and the composition described above.
3 In the following examples, part and % mean part by weight and % by weight, 4 respectively, unless otherwise mentioned. The Mooney viscosity (ML1+4 (~130~ C) ofthe elastomeric composition was measured in accordance with the method of Japanese Industrial 6 Standard K6300 at 130~ C. As the index for hysteresis loss and rolling resistance of a 7 vulc~ni7~te of the elastomeric composition, tan delta (50 ~ C.) was used. An elastomeric 8 composition having a smaller tan delta was evaluated as having a lower hysteresis loss and a 9 lower rolling resistance. Measurement of tan delta (50 ~ C.) was conducted by using a viscoelasticity measurement apparatus (Dynastat) at a temperature of 50~ C. and a frequency 11 of 1 Hz. Measurement of tan delta (0~ C.) as the index for the wet grip was conducted by 12 using the same apparatus at a temperature of 0~ C. and a frequency of 1 Hz.
13 Fracture properties and 300% modulus (M300) were measured in accordance with the 14 method of Japanese Industrial Standard K6301. Abrasion resistance was measured by using a Lambourn abrasion tester at room temperature with a slip rate of 65%. The rolling resistance, 16 wet traction, dry traction and wear of the tires formed in the following examples were 17 measured by standard techniques versus a standard tire filled with Si-69 (Comparative 18 Example 8).
19 The following examples are submitted for the purpose of further illustrating the nature of the present invention and should not be regarded as a limitation on the scope thereof.
21 Preparation of N-Lithiohexamethyleneimine Initiator Solution in Cyclohexane 22 Hexamethyleneimine was distilled from calcium hydride and transferred under 23 nitrogen to a dried, nitrogen-purged bottle. The N-lithio salt of hexamethylene imine was prepared by treating 30 mequiv. of a 2.24 M solution of the cyclic amine in 85: 15 2 cyclohexane:hexane with 30 mequiv. of a 1.67 M solution of n-butyllithium, swirling the 3 mixture at room temperature overnight. The resulting solution was a clear, pale yellow. The 4 solution was stable for several days at room temperature. Samples were drawn from it by syringe for use in initiating polymerization.
6 The following examples display the preparation of polymers from amino-cont~inin~
7 initiators under various conditions.
8 Polymerization Procc~ ,s Conducted in Bottles 9 An initiator mixture made in the above manner was transferred by syringe to a 28-oz.
bottle, containing a blend of butadiene/styrene at 10-25% (w/w) in hexane, at a level of 0.5-11 1.2 meq Li/100 g monomer, and also in the presence of an effective amount of polar modifier 12 (for example, 0.6 mol of N,N,N',N'-tetramethylethylene diamine (TMEDA) per mol of 13 lithium). Optionally, a small amount of an alkoxide salt of Na or K was also added, to 14 modify the sequence distribution of the styrene (for example, 0.05 mol of potassium t-amylate (as a solution in cyclohexane) per mol of lithium). In such a case, a reduced amount 16 of polar modifier was used (for example, 0.15 moles of TMEDA, or 0.06 moles of an 17 oligomeric oxolanyl propane, per mole of lithium). The initiator mixture may optionally be 18 prepared in situ in the presence of the monomers by adding an equivalent or slightly deficient 19 amount of purified secondary amine (e.g, about 0.4-1 mole of amine per mole of alkyllithium). The mixture was agitated at room temperature to 80~C for 15 min to 16 hr, 21 with the polymerization proceeding at a conversion rate of greater than 90% of monomer to 22 polymer. The contents of the bottle containing living polymer cement was then treated with a 23 hexane solution of SnCI4 for an additional 0 - 30 min at 30-80 ~C at a total level of 0.15 to 0.35 moles of Cl per mole of Li. The polymer cement which includes Sn coupled polymer 2 and living cement was treated with a hexane solution of tetraethoxysilane (TEOS) for an 3 additional 20-90 min at 30-80~ C at a level of 0.5-0.7 moles of Si per mole of Li. The cement 4 was then quenched with 2-ethylhexanoic acid(EHA) at a level of 0.5-2.0 moles per mole of Li and a small amount of antioxidant, for example, with 3 ml of a mixture cont~ining 7.0 wt %
6 DBPC, coagulated in i-PrOH, then drum-dried.
7 Procedure for the Preparation of Polymers A to E and Comparative Polymers F to I
8 Used in Examples 1 to 8 and Comparative Examples 1 to 9 9 The same general polymerization procedure was followed to prepare nine polymers (A to I) except where noted below. In each of nine runs, a dried, stainless-steel, 100 gallon 11 reactor, under a nitrogen atmosphere, was charged with 285 lbs. of hexane, 215 lbs. of a blend 12 of 33% by weight styrene in hexane, and 84 lbs. of a blend of 31 % by weight butadiene in 13 hexane. Butyl lithium was charged at a level of 0.947 mmol/100 g of monomer in the 14 preparation of polymer cements A, B, C, D, E, F, G and I and in a slightly lower amount in the prep~ion of polymer cement H, followed by a charge of 0.85 mmol of 16 hexamethyleneimine, and 0.19 mmol of 2,2-bis(2-oxolanyl)propaneas a polar modifier. The 17 polymerization mixture was agitated and heated from 30~C to about 80 ~ 10~C for a period 18 of from 0.4 to 2 hr, depending on temperature, with the polymerization proceeding at a 19 conversion rate of greater than 90% conversion of monomer to polymer. Polymerization at temperatures above 90 ~C should be avoided. After an additional 9.1 lbs of the 31 %
21 butadiene/hexane blend was added to the reactors containing polymer cements A, B, C and D, 22 these mixtures were treated with a hexane solution of SnCl4 for 15 minutes then with a 23 hexane solution of alkoxysilane (TEOS) for an additional 15-120 minutes. Polymer cement E

was simultaneously treated with a hexane solution of SnCl4 and a hexane solution of 2 alkoxysilane(TEOS) for 90 minutes. Comparative polymer cement F was not treated with a 3 hexane solution of SnCl4 but was terminated only with a hexane solution of alkoxysilane 4 (TEOS) for 90 minutes. Comparative polymer cements G and H were treated after the 9.1 Ib addition of 31% butadiene/hexane blend with a hexane solution of SnCI4 for 15-90 minutes 6 but were not treated with a hexane solution of alkoxysilane (TEOS). Comparative polymer 7 cement I was terrnin~ted with a hexane solution of alkoxysilane(TEOS) for 30 minutes at 8 50-80~C prior to treatment with a hexane solution of SnCl4. After production all cements A-I
9 were then transferred and treated with 2-ethylhexanoic acid (EHA) (except for polymer cements G and H), and an antioxidant, and coagulated in i-PrOH, then drum-dried. Polymers l l A to I were formed from cements A to I, respectively. Polymer J, used in Comparative 12 Example No. 8 was a butyl lithium initiated, SnCI4 termin~ted SBR (20% styrene, 60% vinyl 13 and 90 Gum Mooney control polymer). Polymers A to E represent polymers formed 14 according to the process of the present invention and Polymers F to J were prepared for comparative evaluation.
16 Ratios of these SnCl4 and alkoxysilane(TEOS) reactants used in modifying the 17 polymers produced by this process are displayed in Tables 2A, 2B and 3. Table 1 18 summarizes compounding formulations AA and BB used for tire compositions in which the 19 SBR is the tin-coupled and /or siloxane functionalized polymer produced in the cements A-I.
Formulations AA and BB employ either a silica filler having a small portion of carbon 21 black(HAF) or a mixture of carbon black and silica at a weight ratio of 54/46. Examples 1 22 to 5 in Table 2A display the use of Polymers A to E, respectively, in formulation BB having a 23 mixture of carbon black and silica at a weight ratio of 54/46. Comparative Examples 1 to 4 in Table 2B displays the use of comparative Polymers F to I in formulation BB having a 2 mixture of carbon black and silica at a weight ratio of 54/46. Suitable characterizations and 3 evaluations including compound properties of the resultant formulations were then performed 4 and are also displayed in Tables 2A and 2B. Examples 6 and 7 in Table 3 display the use of 5 Polymers A and D, respectively, in formulation AA, having a mixture of a lower amount of 6 carbon black, with silica and Si-69. Comparative Examples 5, 6 and 7 in Table 3 7 likewisedisplay the use of comparative Polymers F, G and H, respectively, in formulation 8 AA. Suitable characterizations and evaluations including compound properties of the 9 resultant formulations were then performed and are also displayed in Table 3.
Table 4 displays examples of tire test data using tread compound having a carbon 11 black to silica ratio of 54 to 46 using formulation BB from Table 1. Example 8 in Table 4 12 displays the use of Polymer D in formulation BB having a mixture of carbon black and 13 silica at a weight ratio of 54/46 and its use in a tire tread. Comparative Examples 8 and 9 in 14 Table 4 displays the use of comparative Polymers J and F in formulation BB having a 15 mixture of carbon black and silica at a weight ratio of 54/46 and compare their use in a tire 16 tread. Suitable characterizations and evaluations of their use in tire treads as shown in Table 17 4.

19 Formulation AA BB
pbw pbw 22 Natural Rubber 25 25 23 Silica 60 30 24 Carbon Black* 6 35 Oil 1 9 22.5 26 Anti-oxidant 0.95 0.95 27 Stearic Acid 1-5 1.5 28 Si-69 2 0 Cure Package 5.25 5.25 Sulfur 3.0~3.6 2.5~3.0 3 *HAF

2 Carbon Black/Silica = 54/46 in Formulation BB
3 Example No. 1 2 3 4 5 4 Polymer Used A B C D E
S CouplerSnCl4~ SnCl4~ SnCl4~ SnCl4~ SnCl 6 Tçrmin~tor TEOS TEOS TEOS TEOS TEOS
7 Sn/Si 30/70 15/85 25/75 5/65 30/70 8 Cl ***/Li 0.3 0.15 0.25 0.35 0.3 9 Si****/Li 0.5 0.68 0.6 0.61 0.5 EHA/Li Ratio 11 GumMLl+4 100~C 61 62 63 53 48 12 Compound Properties 13 Compound MLl+4 a 68 68 67 58 72 14 50~C tan delta 0.121 0.121 0.108 0.1090.098 O~C tan delta 0.227 0.215 0.212 0.1850.224 17 Tb (psi) 2430 3090 2540 2900 3010 18 Eb (%) 392 433 422 426 388 19 Lambourn 65% slip 101 107 104 104 103 20 * Addedbefore TEOS
21 * ~ Added simultanuously 22 ***0f SnCl4 23 ****Of TEOS
24 a atl30~C

2 Carbon Black/Silica = 54/46 in Formulation BB

4 Comparative Example No. 1 2 3 4 Polymer Used F G H
6 Coupler None SnC14 SnC14 TEOSa/SnCl4 7 Terminator TEOS None None TEOS
8 Sn/Si 0/100 100/0 100/030/70 9 Cl ***/Li ---- 0.8 0.8 0.3 Si****/Li 0.6 -- -- 0.5 11 EHA/Li (Mole) 12 Gum MLl+4(~loooc 52 59 86 57 13 Compound Properties 14 Compound ML1+4~ 130~C 83 56 78 86 50~C tan delta 0.118 0.134 0.1260.108 16 O~C tan delta 0.200 0.230 0.2360.223 18 Tb (psi) 2830 2410 2530 2960 19 Eb (%) 389 378 364 401 Lambourn Wear Index (65% slip) 100 88 94 103 21 ***0f SnC14 22 ****Of TEOS
23 a Added before SnCl4 2Lab Physical Properties in Silica-filled Blended Rubber Formulation AA from Table 1 A
3 Example No. 6 7 4 Comparative Example No. 5 6 7 Polymer Used F A D G H
6 Sn/Si Modification Ratio 0/100 30/70 35/65100/0 100/0 7 Cl (of SnCL4) / Li Ratio 0 0.3 0.35 0.8 0.8 8 Si (of TEOS) / Li Ratio 0.6 0.5 0.61 0 0 9 EHA / Li Ratio 1 1 1 0 0 Gum MLl+4 52 58 53 59 86 11 Compound Property 12 130~C MLl+4 58 46 47 43 59 13 50~C tan delta 0.090 0.085 0.0850.097 0.086 Tb (psi) 2450 2260 2140 2080 2350 16 Eb (%) 1399 370 351 1367 390 17 Larnbourn 65% slip 100 98 98 87 95 2Examples of Tire Test Data Using Carbon Black/Silica = 54/46 Tread Compound 3and Formulation BB from Table lA

effects on wet grip (tan delta at 0~ C.).
2 Fig. 1 displays the base polymer GPC data of the polymer of Example 1 before SnCl4 3 coupling had occurred. The area (%) under P, is 91% with a peak molecular weight (Mp) of 4 107,000. The area (%) under P2 is 9% with a peak molecular weight (Mp) of 235,000.
Fig. 2 displays the polymer GPC data of the polymer of Example 1 after SnCl4 coupling 6 had occurred. The area (%) under Pl is 56% with a peak molecular weight (Mp) of 111,000. The 7 area (%) under P2 is 12% with a peak molecular weight (Mp) of 240,000. The area (%) under P3 8 is 32% with a peak molecular weight (Mp) of 399,000.
9 Fig. 3 displays the polymer GPC data of the polymer of Example 1 after both SnCl4 and TEOS coupling had occurred sequentially. The area (%) under P, is 47% with a peak molecular 11 weight (Mp) of 113,000. The area (%) under P2 is 13% with a peak molecular weight (Mp) of 12 248,000. The area (%) under P3 iS 40% with a peak molecular weight (Mp) of 408,000.
13 Fig.4 displays the polymer GPC data of the polymer of Example 5 after both SnCI4 and 14 TEOS coupling had occurred simultaneously. The area (%) under P, iS 31 % with a peak molecular weight (Mp) of 141,000. The area (%) under P2 is 32%with a peak molecular weight 16 (Mp) of 329,000. The area (%) under P3 iS 29% with a peak molecular weight (Mp) of 643,000.
17 The area (%) under P4 is 8% with a peak molecular weight (Mp) of 1,402,000.
18 Fig. 5 displays the polymer GPC data of the polymer of Example 4 after both SnCl4 and 19 TEOS coupling had occurred sequentially. The area (%) under P~ is 34% with a peak molecular weight (Mp) of 93,000. The area (%) under P2 is 66% with a peak molecular weight (Mp) of 21 260,000.
22 Fig. 6 displays the polymer GPC data of the polymer of Example 4 after both SnCI4 and 23 TEOS coupling had occurred sequentially and the coupled polymer had been treated with HCI to break down the Sn-C bonding in the Sn coupled portion of the polymer. The area (%) under P
2 is 59% with a peak molecular weight (Mp) of 104,000. The area (%) under P2 is 41% with a 3 peak molecular weight (Mp) of 214,000.
4 The effects of the elastomeric composition comprising the functionalized polymer can be more clearly seen by comparing the Compound ML 1+4 (with lower numbers being better) and 6 other physical properties or tire properties of the examples and the comparative examples. The 7 differences are a~palell~ from: ( 1 ) the effect of the presence/absence of the functional group 8 cont~ining tin in the functionalized polymer (functional groups are present in the polymers of 9 Examples 1 to 5 as compared with functional groups are absent in the polymer of Cvnlpaldlive Example 1) where the presence of the functional group cont~ining tin in the functionalized 11 polymer offers equivalent physical properties with reduced Compound ML 1+4 which 12 exemplifies improved processability; (2) the effect of the presence/absence of the alkoxysilane 13 group in the functionalized polymer (present in Examples 1 to 5 as compared with absent in 14 Comparative Examples 2 to 3) where the presence of the alkoxysilane group in the functionalized polymer offers improved tan delta at 50~C meaning lower rolling resistance, 16 higher tensile strength (Tb) and improved Lambourn Wear Index; the combined effect of the 17 presence/absence ofthe sequentially or simultaneously added functional groups cont~ining tin 18 and the alkoxysilane group in the functionalized polymer (present in Examples 1 to 5 as 19 compared with alkoxysilane groups added prior to the tin coupling agent in Comparative Example 4) where the sequential or simultaneous addition of Sn and TEOS offers lower 21 Compound ML 1+4, exemplifying improved processability, at the equivalent physical property 22 level.

Claims

1. A method for preparing a diene polymer or copolymer having improved balance in raw polymer viscosity and mixed compound viscosity and adapted to form elastomer compositions useful in tire tread compositions which contains a white carbon as one of the filler comprising the steps in sequence of:
(a) preparing a living diene polymer or copolymer containing active organoalkali or organoalkaline earth metal terminals by anionically polymerizing a conjugated diene monomer or mixture of a conjugated diene monomer and vinyl aromatic hydrocarbon monomer in a hydrocarbon solvent using an organoalkali metal or organoalkaline earth metal initiator;
(b) coupling from about 10 to about 70 percent by weight of the living diene polymer or copolymer chains by reacting the organoalkali or organoalkaline earth metal terminals thereof with from about 0.1 to about 0.7 equivalents of a tin polyhalide, based on the number of halogen atoms in said tin polyhalide, per mole of said living diene polymer or copolymer chains, said tin polyhalide having the general formula Ra SnX b, wherein R is selected from the group consisting of alkyl, alkenyl, cycloalkyl and aryl groups, X is a halogen atom, a is an integer of 0-2 and b is an integer of 2-4; and (c) terminating the remaining living diene polymer or copolymer chains by reacting the organoalkali or organoalkaline earth metal terminals thereof with from about 0.3 to about 2 moles of a hydrocarboxysilane compound.

2. The method of claim 1 wherein said living diene polymer or copolymer is a living polymer of butadiene or a copolymer of butadiene and styrene.

3. The method of claim 1 wherein said tin polyhalide is selected from the group consisting of methyltrichlorotin, dimethyldichlorotin, ethyltrichlorotin, diethyldichlorotin, butyltrichlorotin, dibutyldichlorotin, octyltrichlorotin, dioctyldichlorotin, methyltribromotin, dimethyldibromotin, octyltribromotin, tin tetrachloride, tin tetrabromide, tin tetraiodide, cyclohexyl trichlorotin, phenyl trichlorotin, 1,2-bis (trichlorostannyl) ethane, 1,2-bis (methyldichlorostannyl) ethane, 1,4-bis (trichlorostannyl) butane and 1,4-bis (methyldichlorostannyl) butane.

4. The method of claim 1 wherein said tin polyhalide is tin tetrachloride.

5. The method of claim 1 wherein said tin polyhalide is dibutyldichlorotin.

6. The method of claim 1 wherein said hydrocarboxysilane compound is selected from the group consisting of substituted or unsubstituted tetraalkoxysilane compounds, alkylalkoxysilane compounds, arylalkoxysilane compounds, an alkenylalkoxysilane compounds, and halogenoalkoxysilane compounds.

7. The method of claim 1 wherein said hydrocarboxysilane compound is represented by the formula:

wherein R3 and R4 represent a group selected from an substituted or unsubstituted aliphatic hydrocarbon group, an alicyclic hydrocarbon group, and an aromatic hydrocarbon group, each group having 20 or less carbon atoms, and R4 may be a halo group and y represents an integer of 1 to 4.

8. A diene polymer or copolymer composition comprising a mixture of:
(a) from about 10 to about 70 percent by weight of a diene polymer or copolymer of a diene monomer and a vinyl aromatic hydrocarbon monomer containing carbon-tin bonds in the main polymer or copolymer chain; and (b) from about 90 to about 30 percent by weight of a diene polymer or copolymer of a diene monomer and a vinyl aromatic hydrocarbon monomer containing terminals formed by reacting living diene polymer or copolymer chains having organoalkali or organoalkaline earth metal terminals with a hydrocarboxysilane compound.

9. The composition of claim 8 wherein said diene polymer is polybutadiene.

10. The composition of claim 8 wherein said copolymer is a copolymer of butadiene and styrene.

11. The composition of claim 8 wherein said diene polymer or copolymer containing carbon-tin bonds is formed by coupling living diene polymer or copolymer chains by reacting the organoalkali or organoalkaline earth metal terminals thereof with a tin polyhalide having the general formula Ra SnXb, wherein R is selected from the group consisting of alkyl, alkenyl, cycloalkyl and aryl groups, X is a halogen atom, a is an integer of 0-2 and b is an integer of 2-4.

12. The composition of claim 11 wherein said tin polyhalide is selected from the group consisting of methyltrichlorotin, dimethyldichlorotin, ethyltrichlorotin, diethyldichlorotin, butyltrichlorotin, dibutyldichlorotin, octyltrichlorotin, dioctyldichlorotin, methyltribromotin, dimethyldibromotin, octyltribromotin, tin tetrachloride, tin tetrabromide, tin tetraiodide, cyclohexyl trichlorotin, phenyl trichlorotin, 1,2-bis (trichlorostannyl) ethane, 1,2-bis (methyldichlorostannyl) ethane, 1 ,4-bis (trichlorostannyl) butane and 1,4-bis (methyldichlorostannyl) butane.

13. The composition of claim 11 wherein said tin polyhalide is tin tetrachloride.

14. The composition of claim 11 wherein said tin polyhalide is dibutyldichlorotin.

15. The composition of claim 8 wherein said hydrocarboxysilane compound is selected from the group consisting of substituted or unsubstituted tetraalkoxysilane compounds, alkylalkoxysilane compounds, arylalkoxysilane compounds, an alkenylalkoxysilane compounds, and halogenoalkoxysilane compounds.

16. The compositions of claim 8 wherein said hydrocarboxysilane compound is represented by the formula:

wherein R3 and R4 represent a group selected from an substituted or unsubstituted aliphatic hydrocarbon group, an alicyclic hydrocarbon group, and an aromatic hydrocarbon group, each group having 20 or less carbon atoms, and R4 may be a halo group and y represents an integer of 1 to 4.

17. An elastomer composition adapted for use in forming the treads of tires having highly balanced wet traction, rolling resistance, ice and snow traction, and fracture property comprising:
(a) from 20-100 percent by weight of a diene polymer or copolymer composition which comprises a mixture of:
(i) from about 10 to about 80 percent by weight of a diene polymer or copolymer of a diene monomer and a vinyl aromatic hydrocarbon monomer containing carbon-tin bonds in the main polymer or copolymer chain; and (ii) from about 90 to about 20 percent by weight of a diene polymer or copolymer of a diene monomer and a vinyl aromatic hydrocarbon monomer containing terminals formed by reacting living diene polymer or copolymer chains having organoalkali or organoalkaline earth metal terminals with an hydrocarboxysilane compound selected from the group consisting of unsubstituted and substituted tetraalkoxysilane compounds, alkylalkoxysilane compounds, arylalkoxysilane compounds, an alkenylalkoxysilane compounds, and halogenoalkoxysilane compounds; and (b) from 0-80 percent by weight of a rubber selected from the group consisting of natural rubber, polybutadiene rubber, styrene-butadiene rubber and mixtures thereof.

18. The elastomer composition of claim 17 wherein the diene polymer of component (a) is polybutadiene.

19. The elastomer composition of claim 17 wherein the diene copolymer of component (a) is a copolymer of butadiene and styrene.

20. The elastomer composition of claim 17 wherein said diene polymer or copolymer containing carbon-tin bonds is formed by coupling living diene polymer or copolymer chains by reacting the organoalkali or organoalkaline earth metal terminals thereof with a tin polyhalide having the general formula Ra SnXb, wherein R is selected from the group consisting of alkyl, alkenyl, cycloalkyl and aryl groups, X is a halogen atom, a is an integer of 0-2 and b is an integer of 2-4.

21. The elastomer composition of claim 20 wherein said tin polyhalide is selected from the group consisting of methyltrichlorotin, dimethyldichlorotin, ethyltrichlorotin, diethyldichlorotin, butyltrichlorotin, dibutyldichlorotin, octyltrichlorotin, dioctyldichlorotin, methyltribromotin, dimethyldibromotin, octyltribromotin, tin tetrachloride, tin tetrabromide, tin tetraiodide, cyclohexyl trichlorotin, phenyl trichlorotin, 1,2-bis (trichlorostannyl) ethane, 1,2-bis (methyldichlorostannyl) ethane, 1,4-bis (trichlorostannyl) butane and 1,4-bis (methyldichlorostannyl) butane.

22. The elastomer composition of claim 20 wherein said tin polyhalide is tin tetrachloride.

23. The elastomer composition of claim 20 wherein said tin polyhalide is dibutyldichlorotin.

24. The elastomer composition of claim 17 wherein said said hydrocarboxysilane compound is represented by the formula:

Si(R4)(4-y)(OR3)(y) wherein R3 and R4 represent a group selected from an substituted or unsubstituted aliphatic hydrocarbon group, an alicyclic hydrocarbon group, and an aromatic hydrocarbon group, each group having 20 or less carbon atoms, and R4 may be a halo group and y represents an integer of 1 to4.

25. The elastomer composition of claim 17 wherein said hydrocarboxysilane compound is selected from the group consisting of substituted or unsubstituted tetraalkoxysilane compounds, alkylalkoxysilane compounds, arylalkoxysilane compounds, an alkenylalkoxysilane compounds, and halogenoalkoxysilane compounds.

26. The elastomer composition of claim 17 wherein said hydrocarboxysilane compound is selected from the group consisting of: tetramethoxysilane, tetraethoxysilane, tetra-n-propoxysilane, tetra-n-butoxysilane, tetra(2-ethylhexanoxy)silane, tetraphenoxysilane, tetratoluyloxysilane, methyltrimethoxysilane, methyltriethoxysilane, methyltri-n-propoxysilane, methyltri-n-butoxysilane, methyltriphenoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, ethyltri-n-propoxysilane, ethyltri-n-butoxysilane, ethyltriphenoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, dimethyldi-n-propoxysilane, dimethyldi-n-butoxysilane, dimethyldiphenoxysilane, diethyldimethoxysilane, diphenyldimethoxysilane, 3-glycidoxypropyltrimethoxysilane (GPMOS), .gamma.-methacryloxy propyl trimethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, phenyltri-n-propoxysilane, phenyltri-n-butoxysilane, phenyltriphenoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, vinyltri-n-propoxysilane, vinyltri-n-butoxysilane, vinyltriphenoxysilane, allyltrimethoxysilane, octenyltrimethoxysilane, divinyldimethoxysilane, styryltrimethoxysilane, trimethoxychlorosilane, triethoxychlorosilane, tri-n-propoxychlorosilane, tri-n-butoxychlorosilane, triphenoxychlorosilane, dimethoxydichlorosilane, diethoxydichlorosilane, di-n-propoxydichlorosilane, diphenoxydichlorosilane, methoxytrichlorosilane, ethoxytrichlorosilane, n-propoxytrichlorosilane, phenoxytrichlorosilane, trimethoxybromosilane, triethoxybromosilane, tri-n-propoxybromosilane, triphenoxybromosilane, dimethoxydibromosilane, diethoxydibromosilane, di-n-propoxydibromosilane, diphenoxydibromosilane, methoxytribromosilane, ethoxytribromosilane, n-propoxytribromosilane, phenoxytribromosilane, trimethoxyiodosilane, triethoxyiodosilane, tri-n-propoxyiodosilane, triphenoxyiodosilane, dimethoxydiiodosilane, di-n-propoxydiiodosilane, diphenoxydiiodosilane, methoxytriiodosilane, ethoxytriiodosilane, n-propoxytriiodosilane, phenoxytriiodosilane, bis(trimethoxysilane)-ether, and (bis-( 3-{triethoxysilyl}- propyl)-tetrasulfide).

27. An elastomer composition adapted for use in forming the treads of tires having highly balanced wet traction, rolling resistance, ice and snow traction, and fracture property comprising a rubber material containing a functionalized copolymer in an amount of 10 or more parts by weight in 100 parts by weight of the rubber material, and a filler in an amount of 10 to 150 parts by weight based on 100 parts by weight of the rubber material comprising:
(a) from 20-100 percent by weight of a diene polymer or copolymer composition which comprises a mixture of:
(i) from about 10 to about 80 percent by weight of a diene polymer or copolymer of a diene monomer and a vinyl aromatic hydrocarbon monomer containing carbon-tin bonds in the main polymer or copolymer chain; and (ii) from about 90 to about 20 percent by weight of a diene polymer or copolymer of a diene monomer and a vinyl aromatic hydrocarbon monomer containing terminals formed by reacting living diene polymer or copolymer chains having organoalkali or organoalkaline earth metal terminals with an hydrocarboxysilane compound selected from the group consisting of unsubstituted and substituted tetraalkoxysilane compounds, alkylalkoxysilane compounds, arylalkoxysilane compounds, an alkenylalkoxysilane compounds, and halogenoalkoxysilane compounds; and (b) from 0-80 percent by weight of a rubber selected from the group consisting of natural rubber, polybutadiene rubber, styrene-butadiene rubber and mixtures thereof, and (c) a filler in an amount of 10 to 150 parts by weight based on 100 parts by weight of the rubber material, wherein the filler contains a white carbon.

28. The elastomeric composition according to claim 27, wherein the filler is a white carbon and is present in the composition in an amount of 20 to 90 parts by weight based on 100 parts by weight of the rubber material.

29. The elastomeric composition according to claim 27, wherein the white carbon is silica.

30. The elastomer composition of claim 27 wherein the diene polymer of component (a) is polybutadiene.

31. The elastomer composition of claim 27 wherein the diene copolymer of component (a) is a copolymer of butadiene and styrene.

32. The elastomer composition of claim 27 wherein said diene polymer or copolymer containing carbon-tin bonds is formed by coupling living diene polymer or copolymer chains by reacting the organoalkali or organoalkaline earth metal terminals thereof with a tin polyhalide having the general formula Ra SnXb, wherein R is selected from the group consisting of alkyl, alkenyl, cycloalkyl and aryl groups, X is a halogen atom, a is an integer of 0-2 and b is an integer of 2-4.

33. The elastomer composition of claim 32 wherein said tin polyhalide is selected from the group consisting of methyltrichlorotin, dimethyldichlorotin, ethyltrichlorotin, diethyldichlorotin, butyltrichlorotin, dibutyldichlorotin, octyltrichlorotin, dioctyldichlorotin, methyltribromotin, dimethyldibromotin, octyltribromotin, tin tetrachloride, tin tetrabromide, tin tetraiodide, cyclohexyl trichlorotin, phenyl trichlorotin, 1,2-bis (trichlorostannyl) ethane, 1,2-bis (methyldichlorostannyl) ethane, 1,4-bis (trichlorostannyl) butane and 1,4-bis (methyldichlorostannyl) butane.

34. The elastomer composition of claim 32 wherein said tin polyhalide is tin tetrachloride.

35. The elastomer composition of claim 32 wherein said tin polyhalide is dibutyldichlorotin.

36. The elastomer composition of claim 27 wherein said said hydrocarboxysilane compound is represented by the formula:

Si(R4)(4-y)(OR3)(y) wherein R3 and R4 represent a group selected from an substituted or unsubstituted aliphatic hydrocarbon group, an alicyclic hydrocarbon group, and an aromatic hydrocarbon group, each group having 20 or less carbon atoms, and R4 may be a halo group and y represents an integer of 1 to 4.

37. The elastomer composition of claim 27 wherein said hydrocarboxysilane compound is selected from the group consisting of substituted or unsubstituted tetraalkoxysilane compounds, alkylalkoxysilane compounds, arylalkoxysilane compounds, an alkenylalkoxysilane compounds, and halogenoalkoxysilane compounds.

38. The elastomer composition of claim 27 wherein said hydrocarboxysilane compound is selected from the group consisting of: tetramethoxysilane, tetraethoxysilane, tetra-n-propoxysilane, tetra-n-butoxysilane, tetra(2-ethylhexanoxy)silane, tetraphenoxysilane, tetratoluyloxysilane, methyltrimethoxysilane, methyltriethoxysilane, methyltri-n-propoxysilane, methyltri-n-butoxysilane, methyltriphenoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, ethyltri-n-propoxysilane, ethyltri-n-butoxysilane, ethyltriphenoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, dimethyldi-n-propoxysilane, dimethyldi-n-butoxysilane, dimethyldiphenoxysilane, diethyldimethoxysilane, diphenyldimethoxysilane, 3-glycidoxypropyltrimethoxysilane (GPMOS), .gamma.-methacryloxy propyl trimethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, phenyltri-n-propoxysilane, phenyltri-n-butoxysilane, phenyltriphenoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, vinyltri-n-propoxysilane, vinyltri-n-butoxysilane, vinyltriphenoxysilane, allyltrimethoxysilane, octenyltrimethoxysilane, divinyldimethoxysilane, styryltrimethoxysilane, trimethoxychlorosilane, triethoxychlorosilane, tri-n-propoxychlorosilane, tri-n-butoxychlorosilane, triphenoxychlorosilane, dimethoxydichlorosilane, diethoxydichlorosilane, di-n-propoxydichlorosilane, diphenoxydichlorosilane, methoxytrichlorosilane, ethoxytrichlorosilane, n-propoxytrichlorosilane, phenoxytrichlorosilane, trimethoxybromosilane, triethoxybromosilane, tri-n-propoxybromosilane, triphenoxybromosilane, dimethoxydibromosilane, diethoxydibromosilane, di-n-propoxydibromosilane, diphenoxydibromosilane, methoxytribromosilane, ethoxytribromosilane, n-propoxytribromosilane, phenoxytribromosilane, trimethoxyiodosilane, triethoxyiodosilane, tri-n-propoxyiodosilane, triphenoxyiodosilane, dimethoxydiiodosilane, di-n-propoxydiiodosilane, diphenoxydiiodosilane, methoxytriiodosilane, ethoxytriiodosilane, n-propoxytriiodosilane, phenoxytriiodosilane, bis(trimethoxysilane)-ether, and (bis-(3-{triethoxysilyl}- propyl)-tetrasulfide).