Reinforcement materials, elastomeric compositions and tyres for vehicles wheels comprising the same

US11091607B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11091607-B2
Application numberUS-201716343638-A
CountryUS
Kind codeB2
Filing dateOct 13, 2017
Priority dateOct 26, 2016
Publication dateAug 17, 2021
Grant dateAug 17, 2021

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  5. First independent claim

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Abstract

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The present invention relates to new elastomeric materials for the production of tyres for vehicle wheels with good mechanical properties, in particular high moduli associated with low hysteresis values, including new reinforcement materials. Said reinforcement materials are obtainable by derivatising silica—in-situ during the mixing of the elastomeric composition, or previously—with special silanising agents (A) and silsesquioxanes (B), both substituted with reactive alkenyl functionalities.

First claim

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The invention claimed is: 1. A process for preparing derivatised silica (SIL-A-B) comprising: providing silanised silica (SIL-A), wherein the silanised silica (SIL-A) is made by a process comprising: providing silica (C), providing at least one silanising agent of formula (A), (R1) 3 Si—X  (A) wherein R1, the same or different from each other, are chosen from R2, OR2, OSi(OR2) 3 , OH, halogen, and group X, provided that at least one R1 is equal to OR2, OSi(OR2) 3 , OH, or halogen; R2, the same or different from each other, are chosen from linear and branched alkyl groups with 1 to 20 carbon atoms, cycloalkyl groups with 3 to 20 carbon atoms, alkylaryl groups with 7 to 20 carbon atoms, and aryl groups with 6 to 20 carbon atoms; group X is a reactive alkenyl group chosen from X1, X2, and X3, wherein X1 is a group —R3-C(Wa)═C(R4)R4, X2 is a group —R3-C(R4)=C(Wa)R4, and X3 is a group —R3-Wb-C(R4)=C(R4)R4, wherein  R3 is absent or is chosen from linear and branched alkylene groups with 1 to 10 carbon atoms,  Wa is H or an electron-attractor group chosen from COOR4, CONR4R4, NO 2 , CN, COR4, SO 3 R4, NR4R4, and halogen,  Wb is a group chosen from —O—CO—, —COO—, —NR4-CO—, —CO—NR4-, —SO—, —SO 2 —, and —CO—, and  R4, the same or different from each other, are H or are chosen from the groups R2 defined above, placing the silica (C) and the silanising agent (A) in contact in a first reaction medium, allowing the silica (C) and the silanising agent (A) to react until the silanised silica (SIL-A) is obtained, and separating the silanised silica (SIL-A) from the first reaction medium; placing the silanised silica (SIL-A) in contact, in a second reaction medium, with at least one compound of formula (B) chosen from the silsesquioxanes of formula (B1), (B2), the compounds of formula (B3), and mixtures thereof, wherein n is an even number ranging from 4 to 24, x is an integer ranging from 3 to 23, y is an integer ranging from 1 to 6, and x+y≤24, and groups R, the same or different from each other, are chosen from R2 and X, provided that at least one of groups R is a group X, wherein R2, R4 and X are as defined above; adding at least one radical initiator (D) to the second reaction medium; and allowing the silanised silica (SIL-A), the at least one compound of (B), and the at least one radical initiator (D) to react until a derivatised silica (SIL-A-B) is obtained. 2. The process according to claim 1 , wherein the R3 of group X is chosen from unsaturated alkylene groups. 3. The process according to claim 1 , wherein an acid catalyst is placed in the first reaction medium in contact with the silica (C) and the silanising agent (A). 4. The process according to claim 1 , wherein the at least one silanising agent is a compound of formula (A), (R1) 3 Si—X  (A) wherein R1, the same or different from each other, are chosen from R2 and OR2, and R2 is chosen from linear and branched alkyl groups with 1 to 3 carbon atoms; group X is a reactive alkenyl group X3 as defined above, wherein R3 is an alkylene group with 2 to 5 carbon atoms, Wb is a group —O—CO— and R4, the same or different from each other, are chosen from H and alkyl groups with 1 to 3 carbon atoms. 5. The process according to claim 1 , wherein the compound of formula (B) is a closed cage silsesquioxane of formula (B1) (RSiO 1,5 ) n   (B1) wherein n is an even number ranging from 6 to 12, and all groups R are reactive groups X3 as defined above, wherein R3 is an alkylene group with 2 to 5 carbon atoms, Wb is a group —O—CO— and R4, the same or different from each other, are chosen from H and alkyl groups with 1 to 3 carbon atoms, or all groups R are reactive groups X1 as defined above, wherein R3 is absent, and Wa and R4 are all H. 6. The process according to claim 1 , wherein the silica (C) is an amorphous precipitated silica. 7. The process according to claim 1 , wherein the silanising agent (A) is used in a weight ratio, with respect to silica (C), ranging from 0.05:1 to 1:1. 8. The process according to claim 1 , wherein when preparing the silanised silica (SIL-A), an acid catalyst is used. 9. The process according to claim 1 , wherein the at least one compound of formula (B) is used in a weight ratio, with respect to the silanised silica (SIL-A), ranging from 0.03:1 to 1:1. 10. The process according to claim 1 , wherein the radical initiator (D) is chosen from the class of organic peroxide initiators or from the class of azo compounds. 11. The process according to claim 1 , wherein the first and the second reaction mediums comprise an organic solvent chosen from toluene and one or more alcohols. 12. The process according to claim 11 , wherein the organic solvent is mixed with water. 13. A derivatised silica (SIL-A-B) made by a process comprising: providing silanised silica (SIL-A), wherein the silanised silica (SIL-A) is made by a process comprising: providing silica (C), providing at least one silanising agent of formula (A), (R1) 3 Si—X  (A) wherein R1, the same or different from each other, are chosen from R2, OR2, OSi(OR2) 3 , OH, halogen, and group X, provided that at least one R1 is equal to OR2, OSi(OR2) 3 , OH, or halogen; R2, the same or different from each other, are chosen from linear and branched alkyl groups with 1 to 20 carbon atoms, cycloalkyl groups with 3 to 20 carbon atoms, alkylaryl groups with 7 to 20 carbon atoms, and aryl groups with 6 to 20 carbon atoms; group X is a reactive alkenyl group chosen from X1, X2, and X3, wherein X1 is a group —R3-C(Wa)═C(R4)R4, X2 is a group —R3-C(R4)=C(Wa)R4, and X3 is a group —R3-Wb-C(R4)=C(R4)R4, wherein  R3 is absent or is chosen from linear and branched alkylene groups with 1 to 10 carbon atoms,  Wa is H or an electron-attractor group chosen from COOR4, CONR4R4, NO 2 , CN, COR4, SO 3 R4, NR4R4, and halogen,  Wb is a group chosen from —O—CO—, —COO—, —NR4-CO—, —CO—NR4-, —SO—, —SO 2 —, and —CO—, and  R4, the same or different from each other, are H or are chosen from the groups R2 defined above; placing the silica (C) and the silanising agent (A) in contact in a first reaction medium, allowing the silica (C) and the silanising agent (A) to react until the silanised silica (SIL-A) is obtained, and separating the silanised silica (SIL-A) from the first reaction medium; placing the silanised silica (SIL-A) in contact, in a second reaction medium, with at least one compound of formula (B) chosen from the silsesquioxanes of formula (B1), (B2), the compounds of formula (B3), and mixtures thereof, wherein n is an even number ranging from 4 to 24, x is an integer ranging from 3 to 23, y is an integer ranging from 1 to 6, and x+y≤24, and groups R, the same or different from each other, are chosen from R2 and X, provided that at least one of groups R is a group X, wherein R2, R4 and X are as defined above; adding at least one radical initiator (D) to the second reaction medium; and allowing the silanised silica (SIL-A), the at least one compound of (B), and the at least one radical initiator (D) to react until a derivatised silica (SIL-A-B) is obtained. 14. The derivatised silica (SIL-A-B) according to claim 13 , wherein the at least one compound of formula (B) is present in an amount, expressed as a percentage by weight with respect to the starting silica weight (C), equal to at

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Classifications

  • Silicon-containing compounds · CPC title

  • with silicon-containing compounds · CPC title

  • Silica · CPC title

  • Tread composition · CPC title

  • Oxygen-containing compounds {(C08K5/0091 takes precedence)} · CPC title

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What does patent US11091607B2 cover?
The present invention relates to new elastomeric materials for the production of tyres for vehicle wheels with good mechanical properties, in particular high moduli associated with low hysteresis values, including new reinforcement materials. Said reinforcement materials are obtainable by derivatising silica—in-situ during the mixing of the elastomeric composition, or previously—with special si…
Who is the assignee on this patent?
Pirelli
What technology area does this patent fall under?
Primary CPC classification C08L7/00. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Aug 17 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).