RU2471637C2 - Пневматическая шина - Google Patents
Пневматическая шина Download PDFInfo
- Publication number
- RU2471637C2 RU2471637C2 RU2010108474/11A RU2010108474A RU2471637C2 RU 2471637 C2 RU2471637 C2 RU 2471637C2 RU 2010108474/11 A RU2010108474/11 A RU 2010108474/11A RU 2010108474 A RU2010108474 A RU 2010108474A RU 2471637 C2 RU2471637 C2 RU 2471637C2
- Authority
- RU
- Russia
- Prior art keywords
- group
- rubber
- compound
- carbon atoms
- pneumatic tire
- Prior art date
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- 150000001875 compounds Chemical class 0.000 claims description 110
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- 239000005060 rubber Substances 0.000 claims description 101
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 73
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 70
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 63
- 150000001993 dienes Chemical class 0.000 claims description 47
- 238000000034 method Methods 0.000 claims description 43
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- 238000009833 condensation Methods 0.000 claims description 39
- 230000005494 condensation Effects 0.000 claims description 39
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- 125000004122 cyclic group Chemical group 0.000 claims description 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
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- DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 claims description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 5
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- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 4
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- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 125000003172 aldehyde group Chemical group 0.000 claims description 3
- 125000003368 amide group Chemical group 0.000 claims description 3
- 125000005587 carbonate group Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
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- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 3
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 3
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- 125000005323 thioketone group Chemical group 0.000 claims description 3
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 3
- 150000003606 tin compounds Chemical class 0.000 claims description 3
- NONOKGVFTBWRLD-UHFFFAOYSA-N thioisocyanate group Chemical group S(N=C=O)N=C=O NONOKGVFTBWRLD-UHFFFAOYSA-N 0.000 claims description 2
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- 239000012948 isocyanate Substances 0.000 claims 1
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- 239000003054 catalyst Substances 0.000 description 23
- 238000005299 abrasion Methods 0.000 description 17
- 125000001183 hydrocarbyl group Chemical group 0.000 description 17
- 150000002148 esters Chemical class 0.000 description 15
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- 230000003746 surface roughness Effects 0.000 description 10
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 9
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- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 description 8
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- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 6
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- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Chemical class CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 5
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- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Chemical class CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 5
- 239000005642 Oleic acid Chemical class 0.000 description 5
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Chemical class CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 5
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- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- PUDIUYLPXJFUGB-UHFFFAOYSA-N praseodymium atom Chemical compound [Pr] PUDIUYLPXJFUGB-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- ZILUASOLDUBEBG-UHFFFAOYSA-N propanenitrile;propan-2-one Chemical class CCC#N.CC(C)=O ZILUASOLDUBEBG-UHFFFAOYSA-N 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- OBRKWFIGZSMARO-UHFFFAOYSA-N propylalumane Chemical class [AlH2]CCC OBRKWFIGZSMARO-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 239000002683 reaction inhibitor Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000004439 roughness measurement Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- 229940045105 silver iodide Drugs 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000003746 solid phase reaction Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- FKHIFSZMMVMEQY-UHFFFAOYSA-N talc Chemical compound [Mg+2].[O-][Si]([O-])=O FKHIFSZMMVMEQY-UHFFFAOYSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical class C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- KXLQKNLVPVYVKX-UHFFFAOYSA-J tetrabromorhenium Chemical compound Br[Re](Br)(Br)Br KXLQKNLVPVYVKX-UHFFFAOYSA-J 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- UXMRNSHDSCDMLG-UHFFFAOYSA-J tetrachlororhenium Chemical compound Cl[Re](Cl)(Cl)Cl UXMRNSHDSCDMLG-UHFFFAOYSA-J 0.000 description 1
- KGKLLWHEYDUTBF-UHFFFAOYSA-J tetraiodorhenium Chemical compound I[Re](I)(I)I KGKLLWHEYDUTBF-UHFFFAOYSA-J 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- SQBBHCOIQXKPHL-UHFFFAOYSA-N tributylalumane Chemical compound CCCC[Al](CCCC)CCCC SQBBHCOIQXKPHL-UHFFFAOYSA-N 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- ZIYNWDQDHKSRCE-UHFFFAOYSA-N tricyclohexylalumane Chemical compound C1CCCCC1[Al](C1CCCCC1)C1CCCCC1 ZIYNWDQDHKSRCE-UHFFFAOYSA-N 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- KMLVDTJUQJXRRH-UHFFFAOYSA-N triethoxy(2-pyridin-2-ylethyl)silane Chemical compound CCO[Si](OCC)(OCC)CCC1=CC=CC=N1 KMLVDTJUQJXRRH-UHFFFAOYSA-N 0.000 description 1
- LENYMJLFWIMHEP-UHFFFAOYSA-N triethoxy(3-pyrrolidin-1-ylpropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN1CCCC1 LENYMJLFWIMHEP-UHFFFAOYSA-N 0.000 description 1
- YAFSZVPWWKWGLT-UHFFFAOYSA-N triethoxy(sulfinylmethyl)silane Chemical compound CCO[Si](OCC)(OCC)C=S=O YAFSZVPWWKWGLT-UHFFFAOYSA-N 0.000 description 1
- NDMBIXHWJKTSRM-UHFFFAOYSA-N triethoxy-[1-(2-triethoxysilylpropyltetrasulfanyl)propan-2-yl]silane Chemical compound CCO[Si](OCC)(OCC)C(C)CSSSSCC(C)[Si](OCC)(OCC)OCC NDMBIXHWJKTSRM-UHFFFAOYSA-N 0.000 description 1
- SCONUHVNGPLTMV-UHFFFAOYSA-N triethoxy-[10-(2h-1,3-oxazol-3-yl)decyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCCCCCCCCN1COC=C1 SCONUHVNGPLTMV-UHFFFAOYSA-N 0.000 description 1
- UDUKMRHNZZLJRB-UHFFFAOYSA-N triethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OCC)(OCC)OCC)CCC2OC21 UDUKMRHNZZLJRB-UHFFFAOYSA-N 0.000 description 1
- RWJUTPORTOUFDY-UHFFFAOYSA-N triethoxy-[2-(oxiran-2-ylmethoxy)ethyl]silane Chemical compound CCO[Si](OCC)(OCC)CCOCC1CO1 RWJUTPORTOUFDY-UHFFFAOYSA-N 0.000 description 1
- FBBATURSCRIBHN-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyldisulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSCCC[Si](OCC)(OCC)OCC FBBATURSCRIBHN-UHFFFAOYSA-N 0.000 description 1
- KLFNHRIZTXWZHT-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyltrisulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSSCCC[Si](OCC)(OCC)OCC KLFNHRIZTXWZHT-UHFFFAOYSA-N 0.000 description 1
- HPEPIADELDNCED-UHFFFAOYSA-N triethoxysilylmethanol Chemical compound CCO[Si](CO)(OCC)OCC HPEPIADELDNCED-UHFFFAOYSA-N 0.000 description 1
- ORYGRKHDLWYTKX-UHFFFAOYSA-N trihexylalumane Chemical compound CCCCCC[Al](CCCCCC)CCCCCC ORYGRKHDLWYTKX-UHFFFAOYSA-N 0.000 description 1
- GCZKMPJFYKFENV-UHFFFAOYSA-K triiodogold Chemical compound I[Au](I)I GCZKMPJFYKFENV-UHFFFAOYSA-K 0.000 description 1
- XVZMLSWFBPLMEA-UHFFFAOYSA-N trimethoxy(2-pyridin-2-ylethyl)silane Chemical compound CO[Si](OC)(OC)CCC1=CC=CC=N1 XVZMLSWFBPLMEA-UHFFFAOYSA-N 0.000 description 1
- NGLLPRYTJGRGEU-UHFFFAOYSA-N trimethoxy(3-pyrrolidin-1-ylpropyl)silane Chemical compound CO[Si](OC)(OC)CCCN1CCCC1 NGLLPRYTJGRGEU-UHFFFAOYSA-N 0.000 description 1
- DOJMNEJANGDGGG-UHFFFAOYSA-N trimethoxy(sulfinylmethyl)silane Chemical compound CO[Si](OC)(OC)C=S=O DOJMNEJANGDGGG-UHFFFAOYSA-N 0.000 description 1
- SQSDQKFNZWSCJT-UHFFFAOYSA-N trimethoxy(sulfonylmethyl)silane Chemical compound CO[Si](OC)(OC)C=S(=O)=O SQSDQKFNZWSCJT-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- ZNXDCSVNCSSUNB-UHFFFAOYSA-N trimethoxy-[2-(oxiran-2-ylmethoxy)ethyl]silane Chemical compound CO[Si](OC)(OC)CCOCC1CO1 ZNXDCSVNCSSUNB-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- QJOOZNCPHALTKK-UHFFFAOYSA-N trimethoxysilylmethanethiol Chemical compound CO[Si](CS)(OC)OC QJOOZNCPHALTKK-UHFFFAOYSA-N 0.000 description 1
- SPHALHRGAQVBKI-UHFFFAOYSA-N trimethoxysilylmethanol Chemical compound CO[Si](CO)(OC)OC SPHALHRGAQVBKI-UHFFFAOYSA-N 0.000 description 1
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 1
- JOJQVUCWSDRWJE-UHFFFAOYSA-N tripentylalumane Chemical compound CCCCC[Al](CCCCC)CCCCC JOJQVUCWSDRWJE-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- CNWZYDSEVLFSMS-UHFFFAOYSA-N tripropylalumane Chemical compound CCC[Al](CCC)CCC CNWZYDSEVLFSMS-UHFFFAOYSA-N 0.000 description 1
- RTAKQLTYPVIOBZ-UHFFFAOYSA-N tritert-butylalumane Chemical compound CC(C)(C)[Al](C(C)(C)C)C(C)(C)C RTAKQLTYPVIOBZ-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229940102001 zinc bromide Drugs 0.000 description 1
- 229960001939 zinc chloride Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L15/00—Compositions of rubber derivatives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
- B60C1/00—Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
- B60C1/0016—Compositions of the tread
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
- B60C11/00—Tyre tread bands; Tread patterns; Anti-skid inserts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
- B60C11/00—Tyre tread bands; Tread patterns; Anti-skid inserts
- B60C11/14—Anti-skid inserts, e.g. vulcanised into the tread band
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L21/00—Compositions of unspecified rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/26—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
- C08L23/28—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment by reaction with halogens or compounds containing halogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L7/00—Compositions of natural rubber
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
- B60C11/00—Tyre tread bands; Tread patterns; Anti-skid inserts
- B60C11/0008—Tyre tread bands; Tread patterns; Anti-skid inserts characterised by the tread rubber
- B60C2011/0016—Physical properties or dimensions
- B60C2011/0025—Modulus or tan delta
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
- B60C11/00—Tyre tread bands; Tread patterns; Anti-skid inserts
- B60C11/03—Tread patterns
- B60C11/12—Tread patterns characterised by the use of narrow slits or incisions, e.g. sipes
- B60C2011/129—Sipe density, i.e. the distance between the sipes within the pattern
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/30—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
- C08C19/42—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with metals or metal-containing groups
- C08C19/44—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with metals or metal-containing groups of polymers containing metal atoms exclusively at one or both ends of the skeleton
Abstract
Description
Таблица 1-2-2 | |||
Примеры | |||
15 | 16 | 17 | |
Натуральный каучук | 50 | 50 | 50 |
Цис-1,4-полибутадиеновый каучук*1 | 50 | 50 | 50 |
Модифицированный полибутадиеновый каучук*2 | - | - | - |
Бромированный бутилкаучук | - | - | - |
Углеродная сажа*3 | - | - | - |
Углеродная сажа*4 | - | - | - |
Углеродная сажа*5 | 30 | 30 | 30 |
Кремнезем*6 | 30 | 30 | 30 |
Силановый агент сочетания*7 | 3,0 | 3,0 | 3,0 |
Гигилит*8 | 30,0 | - | - |
Веретенное масло | 20,0 | 20,0 | 20,0 |
Стеариновая кислота | 1,0 | 1,0 | 1,0 |
Антиоксидант (TPPD)*3 | 1,0 | 1,0 | 1,0 |
Оксид цинка | 3,0 | 3,0 | 3,0 |
Ускоритель вулканизации (MBTS)*10 | 0,5 | 0,5 | 0,5 |
Ускоритель вулканизации (CBS)*11 | 1,6 | 1,6 | 1,6 |
Сера | 1,5 | 1,5 | 1,5 |
Вспенивающий агент*12 | - | - | - |
Мочевина | - | - | - |
Органическое волокно, содержащее тонкие частицы*13 | - | - | - |
Длина совокупности прорезей (см/см2) | 2,7 | 3,2 | 1,6 |
Е' (-20°С) | 26 | 26 | 26 |
Ходовые свойства на льду | 178 | 172 | 121 |
«Сухие» ходовые свойства | 98 | 100 | 110 |
Стойкость к истиранию | 96 | 95 | 125 |
Шероховатость поверхности (Ra 75) | 27 | 29 | 27 |
Таблица 1-3 | ||||
Пример 18 | Сравнительный пример | |||
2 | 3 | 4 | ||
Натуральный каучук | 50 | 50 | 50 | 50 |
Цис-1,4- полибутадиеновый каучук*1 | - | 50 | 50 | - |
Модифицированный полибутадиеновый каучук*2 | 50 | - | - | 50 |
Бромированный бутилкаучук | - | - | - | - |
Углеродная сажа*3 | - | - | - | - |
Углеродная сажа*4 | 30 | 30 | 30 | 30 |
Углеродная сажа*5 | - | - | - | - |
Кремнезем*6 | 30 | 30 | 30 | 30 |
Силановый агент сочетания*7 | 3,0 | 3,0 | 3,0 | 3,0 |
Гигилит*8 | 40,0 | 15,0 | 0 | 60,0 |
Веретенное масло | 20,0 | 20,0 | 20,0 | 20,0 |
Стеариновая кислота | 1,0 | 1,0 | 1,0 | 1,0 |
Оксид цинка | 3,0 | 3,0 | 3,0 | 3,0 |
Ускоритель вулканизации (MBTS)*10 | 0,5 | 0,5 | 0,5 | 0,5 |
Ускоритель вулканизации (CBS)*11 | 1,6 | 1,6 | 1,6 | 1,6 |
Сера | 1,5 | 1,5 | 1,5 | 1,5 |
Вспенивающий агент*12 | 2,5 | - | - | 2,5 |
Мочевина | 2,5 | - | - | 2,5 |
Органическое волокно, содержащее тонкие частицы*13 | 2 | - | - | 2 |
Длина совокупности прорезей (см/см2) | 2,7 | 4,5 | 2,7 | 2,7 |
Е' (-20°С) | 24 | 24 | 24 | 18 |
Ходовые свойства на льду | 160 | 105 | 90 | 170 |
«Сухие» ходовые свойства | 100 | 90 | 100 | 99 |
Стойкость к истиранию | 90 | 95 | 100 | 80 |
Шероховатость поверхности (Ra 75) | 60 | 13 | 8 | 110 |
Claims (21)
в которой М обозначает оксид или гидроксид по меньшей мере одного металла, выбранного из Al, Mg, Ti и Ca, а x и y оба представляют собой целые числа от 0 до 10 и имеют средний диаметр частиц равный 100 µм или меньше.
где А1 обозначает одновалентную группу, содержащую по меньшей мере одну функциональную группу, выбранную из эпоксигруппы, тиоэпоксигруппы, изоцианатной группы, тиоизоцианатной группы, кетогруппы, тиокетогруппы, альдегидной группы, тиоальдегидной группы, иминогруппы, амидной группы, тригидрокарбил-изоциануратного остатка, остатка эфира карбоновой кислоты, остатка эфира тиокарбоновой кислоты, остатка ангидрида карбоновой кислоты, остатка галогенангидрида карбоновой кислоты и остатка дигидрокарбилкарбоната; R1 обозначает простую связь или двухвалентную неактивную углеводородную группу; R2 и R3 независимо обозначают одновалентную алифатическую углеводородную группу, имеющую от 1 до 20 атомов углерода, или одновалентную ароматическую группу, имеющую от 6 до 18 атомов углерода; n представляет собой целое число от 0 до 2; в случае присутствия нескольких групп OR3 эти группы могут быть одинаковыми или разными; и при этом в молекуле отсутствуют активный протон и ониевая соль.
где А2 обозначает одновалентную группу, содержащую по меньшей мере одну функциональную группу, выбранную из циклической третичной аминогруппы, нециклической третичной аминогруппы, пиридинового остатка, сульфидной группы, полисульфидной группы, нитрильной группы, остатка ониевой соли циклического третичного амина, остатка ониевой соли нециклического третичного амина, группы, содержащей связь аллил-Sn или бензил-Sn, сульфонильной группы, сульфинильной группы; R4 обозначает простую связь или двухвалентную неактивную углеводородную группу; R5 и R6 независимо обозначают одновалентную алифатическую углеводородную группу, имеющую от 1 до 20 атомов углерода, или одновалентную ароматическую группу, имеющую от 6 до 18 атомов углерода; m представляет собой целое число от 0 до 2; и в случае присутствия нескольких групп OR6 эти группы могут быть одинаковыми или разными;
где А3 обозначает одновалентную группу, содержащую по меньшей мере одну функциональную группу, выбранную из гидроксильной группы, тиоловой группы, первичной аминогруппы, остатка ониевой соли первичного амина, циклической вторичной аминогруппы, остатка ониевой соли циклического вторичного амина, нециклической вторичной аминогруппы и остатка ониевой соли нециклического вторичного амина; R7 обозначает простую связь или двухвалентную неактивную углеводородную группу; R8 и R9 независимо обозначают одновалентную алифатическую углеводородную группу, имеющую от 1 до 20 атомов углерода, или одновалентную ароматическую группу, имеющую от 6 до 18 атомов углерода; q представляет собой целое число от 0 до 2; и в случае присутствия нескольких групп OR9 эти группы могут быть одинаковыми или разными.
(1) соль карбоновой кислоты, имеющей от 3 до 30 атомов углерода с оловом в состоянии окисления +2:
Sn(OCOR10)2,
где R10 обозначает органическую группу, имеющую от 2 до 29 атомов углерода, причем в случае присутствия нескольких таких групп они могут быть одинаковыми или разными;
(2) соединение олова со степенью окисления +4, которое отвечает следующей формуле:
R11 rSnA4 tB1 (4-t-r),
где r представляет собой целое число от 1 до 3; t представляет собой целое число, равное 1 или 2; (t+r) представляет собой целое число, равное 3 или 4; R11 обозначает алифатическую углеводородную группу, имеющую от 1 до 30 атомов углерода; В1 обозначает гидроксильную группу или галоген; А4 обозначает группу, выбранную из (а) карбоксильной группы, имеющей от 2 до 30 атомов углерода, (b) 1,3-дикарбонил-содержащей группы, имеющей от 5 до 30 атомов углерода, (с) гидрокарбилоксигруппы, имеющей от 3 до 30 атомов углерода, и (d) силоксигруппы, которая является полностью трехзамещенной (заместители могут быть одинаковыми или разными) углеводородными группами, имеющими от 1 до 20 атомов углерода, и/или гидрокарбилоксигруппами, имеющими от 1 до 20 атомов углерода; причем в случае присутствия нескольких А4 они могут быть одинаковыми или разными; и
(3) соединение титана со степенью окисления +4, которое отвечает следующей формуле:
A5 xTiB2 (4-x),
где x - целое число, равное 2 или 4; А5 обозначает (е) гидроксикарбилоксигруппу или (f) силоксигруппу, которая является полностью трехзамещенной алкильными группами, имеющими от 1 до 30 атомов углерода, и/или гидрокарбилоксигруппами, имеющими от 1 до 20 атомов углерода, причем в случае присутствия нескольких А5 они могут быть одинаковыми или разными; и В2 обозначает 1,3-дикарбонил-содержащую группу, имеющую от 5 до 30 атомов углерода.
компонент (i): соединение, содержащее редкоземельный элемент, соответствующий атомному номеру от 57 до 71 в Периодической таблице элементов, или продукт реакции этого соединения с основанием Льюиса;
компонент (ii): алюмоксан и/или алюминийорганическое соединение формулы AlR12R13R14 (где R12 и R13, одинаковые или разные, обозначают углеводородную группу, имеющую от 1 до 10 атомов углерода, или атом водорода и R14 обозначает углеводородную группу, имеющую от 1 до 10 атомов углерода, при условии, что R14 может быть таким же или отличным от R12 и R13) и
компонент (iii): по меньшей мере одно галогенсодержащее соединение, выбранное из группы, состоящей из кислоты Льюиса, комплексного соединения галогенида металла и основания Льюиса, и органического соединения, содержащего активный галоген.
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