Functionalized hydrogenated interpolymer with non-hydrogenated segment
US-2024279401-A1 · Aug 22, 2024 · US
US2016376394A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016376394-A1 |
| Application number | US-201615203874-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 7, 2016 |
| Priority date | Aug 20, 2014 |
| Publication date | Dec 29, 2016 |
| Grant date | — |
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The present invention is directed to a functionalized elastomer having the formula (P-B n ) q -X where P is a polydiene segment, B is a styrenic monomer residue, n is the number of styrenic monomer residues, and B n is a polystyrenic segment; X is a multifunctional terminator residue, and q is the number of (P-B n ) chains coupled to X; wherein for q=1, the weight percent of the functionalized elastomer is at least 90 percent by weight.
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1 - 11 . (canceled) 12 . A method of making a functionalized elastomer, comprising the steps of polymerizing a diene based monomer in the presence of an anionic polymerization initiator to produce a polydiene anionic living polymer; further polymerizing the polydiene anionic living polymer with from 1 to 10 equivalents of a styrenic monomer per equivalent of initiator to produce a polydiene-polystyrenic anionic living polymer; and terminating the polydiene-polystyrenic anionic living polymer with a terminator to form the functionalized elastomer, wherein the terminator is of formula I wherein R 1 is C1 to C4 linear alkyl, or C1 to C4 branched alkanediyl; in formula I X 1 , X 2 , X 3 are independently S, a group of formula II, or a group of formula III; where R 2 is C1 to C18 linear or branched alkyl; Z is R 3 , —OR 4 , or —R 5 —X 4 ; R 3 , R 4 are independently C1 to C18 linear or branched alkyl; R 5 is C1 to C18 alkanediyl or dialkyl ether diyl, with the proviso when R 5 is C1 to C18 dialkyl ether diyl, X 1 , X 2 , X 3 may be independently O, S, a group of formula II, or a group of formula III; X 4 is halogen or a group of structure IV, V, VI, VII or VIII wherein R 6 , R 7 , R 8 , R 9 , and R 16 are independently H or C1 to C8 alkyl; R 11 is C2 to C8 alkanediyl; R 12 and R 13 are independently H, aryl or C1 to C8 alkyl; X 5 , X 6 , X 7 are independently O, S, or a group of formula II or III where R 2 is C1 to C18 linear or branched alkyl; Q is N or a group of structure IX wherein R 14 is C1 to C8 alkyl. 13 . The method of claim 12 , wherein the diene based monomer is selected from the group consisting of 1,3-butadiene, isoprene, 1,3-pentadiene, 2,3-dimethyl-1,3-butadiene, 2-methyl-1,3-pentadiene, 2,3-dimethyl-1,3-pentadiene, 2-phenyl-1,3-butadiene, and 4,5-diethyl-1,3-octadiene. 14 . The method of claim 12 , wherein the styrenic monomer is selected from the group consisting of styrene, 3-methylstyrene, 3,5-diethylstyrene, 4-propylstyrene, 2,4,6-trimethylstyrene, 4-dodecylstyrene, 3-methyl-5-normal-hexylstyrene, 4-phenylstyrene, 2-ethyl-4-benzylstyrene, 3,5-diphenylstyrene, 2,3,4,5-tetraethylstyrene, and α-methylstyrene. 15 . The method of claim 12 , wherein the diene based monomer is selected from the group consisting of 1,3-butadiene and isoprene, and the styrenic monomer is styrene. 16 . The method of claim 12 , wherein n ranges from 5 to 10. 17 . The method of claim 12 , wherein the polydiene has a molecular weight Mn ranging from 50K to 500K. 18 . (canceled) 19 . (canceled)
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