Resin composition for tires and pneumatic tire
US-2024140139-A1 · May 2, 2024 · US
US9475902B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9475902-B2 |
| Application number | US-201113885220-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 11, 2011 |
| Priority date | Nov 16, 2010 |
| Publication date | Oct 25, 2016 |
| Grant date | Oct 25, 2016 |
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The present invention relates to polymers functionalized by terminal groups, where the polymers have a trialkylsilyloxy group of the formula (I) at the end of the chain, where R 1 , R 2 , and R 3 can be identical or different and are alkyl, cycloalkyl, and aralkyl moieties which can comprise heteroatoms such as O, N, S, and Si.
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The invention claimed is: 1. A process for producing polymers functionalized by terminal groups, the process comprising contacting polymers having reactive chain ends with functionalization reagent comprising one or more bis(trialkylsilyl) peroxides to produce polymers comprising terminal trialkylsilyloxy groups. 2. The process according to claim 1 , further comprising contacting the polymers having reactive chain ends with the functionalization reagent after conclusion of polymerization of the polymers. 3. The process according to claim 1 , further comprising contacting the polymers having reactive chain ends with an excess amount of functionalization reagent. 4. The process according to claim 1 , further comprising contacting the polymers having reactive chain ends with a stoichiometric amount or a sub-stoichiometric amount of functionalization reagent. 5. The process to claim 2 , 3 or 4 , wherein the amount of functionalization reagents is 0.005-2% by weight based on the amount of polymer having reactive polymer than ends. 6. The process according to claim 5 , further comprising contacting the polymers having reactive chain ends with functionalization reagent in the presence of coupling reagents. 7. The process according to claim 1 , wherein the process comprises contacting the polymers having reactive chain ends with bis(trialkylsilyl) peroxide of the formula (II) to produce polymers comprising terminal trialkylsilyloxy groups of the formula (I) where R 1 , R 2 , and R 3 are identical or different and are alkyl, cycloalkyl, and aralkyl moieties which can comprise heteroatoms such as O, N, S, and Si. 8. The process according to claim 7 , wherein: R 1 , R 2 and R 3 are identical and are methyl; the polymer is a polybutadiene, a polyisoprene, a butadiene-isoprene copolymer, a butadiene-styrene copolymer, an isoprene-styrene copolymer, or a butadiene-isoprene-styrene terpolymer; and the process further comprises polymerization of the polymers, and after conclusion of polymerization, contacting of the polymers having reactive chain ends with the functionalization reagent in the presence of a coupling agent; and an amount of functionalization reagent is 0.01-1% by weight, based on the amount of polymer having reactive polymer chain ends, the coupling agent is added prior to the functionalization reagent, at the same time as the functionalization reagent, or after the functionalization reagent; and the coupling agent comprises at least one of: silicon tetrachloride, methyltrichlorosilane, dimethyldichlorosilane, tin tetrachloride, dibutyltin dichloride, tetraalkoxysilanes, ethylene glycol diglycidyl ether, and 1,2,4-tris(chloromethyl)benzene.
Compositions of rubber derivatives (C08L11/00, C08L13/00 take precedence) · CPC title
Compositions of the tread · CPC title
Natural or synthetic rubber or rubber-like compound containing · CPC title
of polymers containing metal atoms exclusively at one or both ends of the skeleton · CPC title
containing hydrolysable silane groups · CPC title
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