TWI441858B - 橡膠組成物,彼之製法及由彼製得之物件 - Google Patents
橡膠組成物,彼之製法及由彼製得之物件 Download PDFInfo
- Publication number
- TWI441858B TWI441858B TW097104334A TW97104334A TWI441858B TW I441858 B TWI441858 B TW I441858B TW 097104334 A TW097104334 A TW 097104334A TW 97104334 A TW97104334 A TW 97104334A TW I441858 B TWI441858 B TW I441858B
- Authority
- TW
- Taiwan
- Prior art keywords
- decane
- group
- rubber
- triethoxydecane
- rubber composition
- Prior art date
Links
- 229920001971 elastomer Polymers 0.000 title claims abstract description 184
- 239000005060 rubber Substances 0.000 title claims abstract description 171
- 239000000203 mixture Substances 0.000 title claims abstract description 132
- 238000000034 method Methods 0.000 title claims abstract description 33
- 230000008569 process Effects 0.000 title abstract description 8
- 239000000945 filler Substances 0.000 claims abstract description 85
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 43
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 38
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 37
- 239000011593 sulfur Chemical group 0.000 claims abstract description 37
- 238000002156 mixing Methods 0.000 claims abstract description 32
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 30
- 239000001257 hydrogen Substances 0.000 claims abstract description 28
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 28
- 125000003118 aryl group Chemical group 0.000 claims abstract description 27
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 25
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 18
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000001301 oxygen Substances 0.000 claims abstract description 14
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 14
- 125000005843 halogen group Chemical group 0.000 claims abstract description 9
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 8
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 126
- -1 vinyl aromatic compound Chemical class 0.000 claims description 67
- 229910000420 cerium oxide Inorganic materials 0.000 claims description 37
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 claims description 36
- 239000006229 carbon black Substances 0.000 claims description 22
- 150000001993 dienes Chemical class 0.000 claims description 16
- 244000043261 Hevea brasiliensis Species 0.000 claims description 15
- 229920003052 natural elastomer Polymers 0.000 claims description 15
- 229920001194 natural rubber Polymers 0.000 claims description 15
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
- 239000000806 elastomer Substances 0.000 claims description 13
- 150000002431 hydrogen Chemical class 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 13
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 12
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 12
- 229920001577 copolymer Polymers 0.000 claims description 11
- 229920002554 vinyl polymer Polymers 0.000 claims description 11
- 239000012190 activator Substances 0.000 claims description 10
- 229920002857 polybutadiene Polymers 0.000 claims description 10
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 9
- 229920000620 organic polymer Polymers 0.000 claims description 9
- NIJWQIMKUKWGEN-UHFFFAOYSA-N 1,1,1-tributoxydecane Chemical compound C(CCC)OC(CCCCCCCCC)(OCCCC)OCCCC NIJWQIMKUKWGEN-UHFFFAOYSA-N 0.000 claims description 8
- 239000005062 Polybutadiene Substances 0.000 claims description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 7
- 125000004122 cyclic group Chemical group 0.000 claims description 7
- 125000000524 functional group Chemical group 0.000 claims description 7
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 7
- 229920001897 terpolymer Polymers 0.000 claims description 6
- AGGJWJFEEKIYOF-UHFFFAOYSA-N 1,1,1-triethoxydecane Chemical compound CCCCCCCCCC(OCC)(OCC)OCC AGGJWJFEEKIYOF-UHFFFAOYSA-N 0.000 claims description 5
- 229910052684 Cerium Inorganic materials 0.000 claims description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 5
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 5
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims description 5
- 229910044991 metal oxide Inorganic materials 0.000 claims description 5
- 150000004706 metal oxides Chemical class 0.000 claims description 5
- 229910052698 phosphorus Inorganic materials 0.000 claims description 5
- 239000011574 phosphorus Substances 0.000 claims description 5
- RLRLMTBPHXOLEH-UHFFFAOYSA-N ClCC1=CC=C(C=C1)CCC(C(OCC)(OCC)OCC)CCCCCCCC Chemical compound ClCC1=CC=C(C=C1)CCC(C(OCC)(OCC)OCC)CCCCCCCC RLRLMTBPHXOLEH-UHFFFAOYSA-N 0.000 claims description 4
- 229920000459 Nitrile rubber Polymers 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 239000000178 monomer Substances 0.000 claims description 4
- 229920003051 synthetic elastomer Polymers 0.000 claims description 4
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims description 3
- CTBFXAXARKCWEI-UHFFFAOYSA-N CCCCCCCC(CCC1=CC(=CC=C1)CBr)C(OC)(OC)OC Chemical compound CCCCCCCC(CCC1=CC(=CC=C1)CBr)C(OC)(OC)OC CTBFXAXARKCWEI-UHFFFAOYSA-N 0.000 claims description 3
- YSLFSOLHUCNMID-UHFFFAOYSA-N CCCCCCCC(CCC1=CC=C(C=C1)C(C)Br)C(OC)(OC)OC Chemical compound CCCCCCCC(CCC1=CC=C(C=C1)C(C)Br)C(OC)(OC)OC YSLFSOLHUCNMID-UHFFFAOYSA-N 0.000 claims description 3
- HXJPYVGLNDNWAZ-UHFFFAOYSA-N CCCCCCCC(CCC1=CC=C(C=C1)C(C)I)C(OC)(OC)OC Chemical compound CCCCCCCC(CCC1=CC=C(C=C1)C(C)I)C(OC)(OC)OC HXJPYVGLNDNWAZ-UHFFFAOYSA-N 0.000 claims description 3
- OBLCSDVKQWVFIT-UHFFFAOYSA-N CCCCCCCCC(C#CCCl)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(C#CCCl)C(OCC)(OCC)OCC OBLCSDVKQWVFIT-UHFFFAOYSA-N 0.000 claims description 3
- FVWPDCZRJUOCGP-UHFFFAOYSA-N CCCCCCCCC(C=CCBr)C(OC)(OC)OC Chemical compound CCCCCCCCC(C=CCBr)C(OC)(OC)OC FVWPDCZRJUOCGP-UHFFFAOYSA-N 0.000 claims description 3
- HYQXXRJBVBRKCY-UHFFFAOYSA-N CCCCCCCCC(C=CCBr)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(C=CCBr)C(OCC)(OCC)OCC HYQXXRJBVBRKCY-UHFFFAOYSA-N 0.000 claims description 3
- VLTZXSSMYOLEGG-UHFFFAOYSA-N CCCCCCCCC(C=CCCl)C(C)(OCC)OCC Chemical compound CCCCCCCCC(C=CCCl)C(C)(OCC)OCC VLTZXSSMYOLEGG-UHFFFAOYSA-N 0.000 claims description 3
- NDZLWHYGEILNPM-UHFFFAOYSA-N CCCCCCCCC(C=CCCl)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(C=CCCl)C(OCCCC)(OCCCC)OCCCC NDZLWHYGEILNPM-UHFFFAOYSA-N 0.000 claims description 3
- VCMBPZLBYRIUHN-UHFFFAOYSA-N CCCCCCCCC(C=CCI)C(OC)(OC)OC Chemical compound CCCCCCCCC(C=CCI)C(OC)(OC)OC VCMBPZLBYRIUHN-UHFFFAOYSA-N 0.000 claims description 3
- QYEPBPBNNGECML-UHFFFAOYSA-N CCCCCCCCC(C=CCI)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(C=CCI)C(OCC)(OCC)OCC QYEPBPBNNGECML-UHFFFAOYSA-N 0.000 claims description 3
- PZFKYEHUTWKFFP-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)C(C)Br)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)C(C)Br)C(OCC)(OCC)OCC PZFKYEHUTWKFFP-UHFFFAOYSA-N 0.000 claims description 3
- VXYDGVDINWFHHL-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)C(C)I)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)C(C)I)C(OCCCC)(OCCCC)OCCCC VXYDGVDINWFHHL-UHFFFAOYSA-N 0.000 claims description 3
- NXWXJQRMBACKDV-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)C(CC)Cl)C(OC)(OC)OC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)C(CC)Cl)C(OC)(OC)OC NXWXJQRMBACKDV-UHFFFAOYSA-N 0.000 claims description 3
- QRQHMWKADOMTAT-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)C(CC)I)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)C(CC)I)C(OCCCC)(OCCCC)OCCCC QRQHMWKADOMTAT-UHFFFAOYSA-N 0.000 claims description 3
- CZMUMPVOYJNNJT-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)CCl)C(OC)(OC)OC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)CCl)C(OC)(OC)OC CZMUMPVOYJNNJT-UHFFFAOYSA-N 0.000 claims description 3
- JFZWZBRKQFERPJ-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)CCl)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)CCl)C(OCCCC)(OCCCC)OCCCC JFZWZBRKQFERPJ-UHFFFAOYSA-N 0.000 claims description 3
- ILYNQZRFFNWMTG-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)CI)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)CI)C(OCC)(OCC)OCC ILYNQZRFFNWMTG-UHFFFAOYSA-N 0.000 claims description 3
- GDYVTGWMUMPKSR-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(C)Br)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(C)Br)C(OCC)(OCC)OCC GDYVTGWMUMPKSR-UHFFFAOYSA-N 0.000 claims description 3
- PPMIKICCHZPQHT-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(C)Br)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(C)Br)C(OCCCC)(OCCCC)OCCCC PPMIKICCHZPQHT-UHFFFAOYSA-N 0.000 claims description 3
- HGEWRWMJJXUZAT-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(C)Cl)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(C)Cl)C(OCC)(OCC)OCC HGEWRWMJJXUZAT-UHFFFAOYSA-N 0.000 claims description 3
- MUUKZJPGGDGKNY-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(C)I)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(C)I)C(OCC)(OCC)OCC MUUKZJPGGDGKNY-UHFFFAOYSA-N 0.000 claims description 3
- SQUDZWRHBXIELP-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(C)I)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(C)I)C(OCCCC)(OCCCC)OCCCC SQUDZWRHBXIELP-UHFFFAOYSA-N 0.000 claims description 3
- PTFLRZYIRAIRIJ-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)Br)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)Br)C(OCC)(OCC)OCC PTFLRZYIRAIRIJ-UHFFFAOYSA-N 0.000 claims description 3
- FKVKHGUIEONYLP-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)Br)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)Br)C(OCCCC)(OCCCC)OCCCC FKVKHGUIEONYLP-UHFFFAOYSA-N 0.000 claims description 3
- JMEZTAYPILZRSF-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)Cl)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)Cl)C(OCC)(OCC)OCC JMEZTAYPILZRSF-UHFFFAOYSA-N 0.000 claims description 3
- XCKFKPNXPWKGPH-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)I)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)I)C(OCC)(OCC)OCC XCKFKPNXPWKGPH-UHFFFAOYSA-N 0.000 claims description 3
- JLUIDZGIKBGVKL-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)I)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)I)C(OCCCC)(OCCCC)OCCCC JLUIDZGIKBGVKL-UHFFFAOYSA-N 0.000 claims description 3
- SBPCIGCWHSMODN-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(Cl)Cl)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(Cl)Cl)C(OCC)(OCC)OCC SBPCIGCWHSMODN-UHFFFAOYSA-N 0.000 claims description 3
- FBBABBJAGNBFEF-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)CBr)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)CBr)C(OCC)(OCC)OCC FBBABBJAGNBFEF-UHFFFAOYSA-N 0.000 claims description 3
- YRYXHOZYTPSUFY-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)CBr)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)CBr)C(OCCCC)(OCCCC)OCCCC YRYXHOZYTPSUFY-UHFFFAOYSA-N 0.000 claims description 3
- DLGBIXIRYMPTDH-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)CCl)C(C)(C)OCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)CCl)C(C)(C)OCC DLGBIXIRYMPTDH-UHFFFAOYSA-N 0.000 claims description 3
- RZARCVVAEKJADS-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)CCl)C(C)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)CCl)C(C)(OCC)OCC RZARCVVAEKJADS-UHFFFAOYSA-N 0.000 claims description 3
- YWVBZDBBVTVXOQ-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)CCl)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)CCl)C(OCCCC)(OCCCC)OCCCC YWVBZDBBVTVXOQ-UHFFFAOYSA-N 0.000 claims description 3
- WZOBZFDZCQRVRR-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)CI)C(OC)(OC)OC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)CI)C(OC)(OC)OC WZOBZFDZCQRVRR-UHFFFAOYSA-N 0.000 claims description 3
- JWXUOBVPXXQGGA-UHFFFAOYSA-N CCOC(CCCCCCCCCCC(CCCCCCCCCC(OCC)(OCC)OCC)CC1=CC=C(C=C1)CCl)(OCC)OCC Chemical compound CCOC(CCCCCCCCCCC(CCCCCCCCCC(OCC)(OCC)OCC)CC1=CC=C(C=C1)CCl)(OCC)OCC JWXUOBVPXXQGGA-UHFFFAOYSA-N 0.000 claims description 3
- 101150065749 Churc1 gene Proteins 0.000 claims description 3
- 102100038239 Protein Churchill Human genes 0.000 claims description 3
- 229910052787 antimony Inorganic materials 0.000 claims description 3
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 3
- 239000000839 emulsion Substances 0.000 claims description 3
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 3
- GFSIDUBQBTXKSX-UHFFFAOYSA-N CCCCCCCC(CCC1=CC(=CC=C1)C(C)I)C(OC)(OC)OC Chemical compound CCCCCCCC(CCC1=CC(=CC=C1)C(C)I)C(OC)(OC)OC GFSIDUBQBTXKSX-UHFFFAOYSA-N 0.000 claims description 2
- YWABENXXJSTWTI-UHFFFAOYSA-N CCCCCCCC(CCC1=CC=C(C=C1)C(CC)Cl)C(OC)(OC)OC Chemical compound CCCCCCCC(CCC1=CC=C(C=C1)C(CC)Cl)C(OC)(OC)OC YWABENXXJSTWTI-UHFFFAOYSA-N 0.000 claims description 2
- ANJUVRUDCNQYMI-UHFFFAOYSA-N CCCCCCCC(CCC1=CC=C(C=C1)C(CC)I)C(OC)(OC)OC Chemical compound CCCCCCCC(CCC1=CC=C(C=C1)C(CC)I)C(OC)(OC)OC ANJUVRUDCNQYMI-UHFFFAOYSA-N 0.000 claims description 2
- IUZOGNDVDNSHTG-UHFFFAOYSA-N CCCCCCCCC(C=CCI)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(C=CCI)C(OCCCC)(OCCCC)OCCCC IUZOGNDVDNSHTG-UHFFFAOYSA-N 0.000 claims description 2
- JNBONWGEOGBLDN-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)C(CC)Cl)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)C(CC)Cl)C(OCC)(OCC)OCC JNBONWGEOGBLDN-UHFFFAOYSA-N 0.000 claims description 2
- UJTHEBBCMMCVLI-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)CBr)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)CBr)C(OCCCC)(OCCCC)OCCCC UJTHEBBCMMCVLI-UHFFFAOYSA-N 0.000 claims description 2
- BSCGYVGLRMKHGR-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)CI)C(OC)(OC)OC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)CI)C(OC)(OC)OC BSCGYVGLRMKHGR-UHFFFAOYSA-N 0.000 claims description 2
- YMBRCJFAUCANBZ-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(C)Cl)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(C)Cl)C(OCCCC)(OCCCC)OCCCC YMBRCJFAUCANBZ-UHFFFAOYSA-N 0.000 claims description 2
- SJWJPLPJYSKVLN-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)Cl)C(OC)(OC)OC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)Cl)C(OC)(OC)OC SJWJPLPJYSKVLN-UHFFFAOYSA-N 0.000 claims description 2
- WDWSZXIMMVTUKR-UHFFFAOYSA-N CCOC(CCCCCCCCCC(CCCCCCCCCC(OCC)(OCC)OCC)CC1=CC=C(C=C1)CCl)(OCC)OCC Chemical compound CCOC(CCCCCCCCCC(CCCCCCCCCC(OCC)(OCC)OCC)CC1=CC=C(C=C1)CCl)(OCC)OCC WDWSZXIMMVTUKR-UHFFFAOYSA-N 0.000 claims description 2
- VCYOVOKJTMESHA-UHFFFAOYSA-N ClCC=CC(C(OC)(OC)OC)CCCCCCCC Chemical compound ClCC=CC(C(OC)(OC)OC)CCCCCCCC VCYOVOKJTMESHA-UHFFFAOYSA-N 0.000 claims description 2
- 150000001336 alkenes Chemical group 0.000 claims description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N chloroform Substances ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 2
- 239000011630 iodine Substances 0.000 claims description 2
- 229910052740 iodine Inorganic materials 0.000 claims description 2
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 239000004408 titanium dioxide Substances 0.000 claims description 2
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 claims 3
- DUWVNJYFICISSW-UHFFFAOYSA-N CCCCCCCC(CCC1=CC=C(C=C1)C(CC)Br)C(OC)(OC)OC Chemical compound CCCCCCCC(CCC1=CC=C(C=C1)C(CC)Br)C(OC)(OC)OC DUWVNJYFICISSW-UHFFFAOYSA-N 0.000 claims 2
- XMVHEPSJRVODFQ-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)C(C)Cl)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)C(C)Cl)C(OCC)(OCC)OCC XMVHEPSJRVODFQ-UHFFFAOYSA-N 0.000 claims 2
- OZHUJNZVFIEXAF-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)C(C)Cl)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)C(C)Cl)C(OCCCC)(OCCCC)OCCCC OZHUJNZVFIEXAF-UHFFFAOYSA-N 0.000 claims 2
- DVUBTYRHJPQFND-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)C(C)I)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)C(C)I)C(OCC)(OCC)OCC DVUBTYRHJPQFND-UHFFFAOYSA-N 0.000 claims 2
- ZVTLGPXTCCWVKM-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)CBr)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)CBr)C(OCC)(OCC)OCC ZVTLGPXTCCWVKM-UHFFFAOYSA-N 0.000 claims 2
- PUSHCJJGJCJBGM-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)CI)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)CI)C(OCCCC)(OCCCC)OCCCC PUSHCJJGJCJBGM-UHFFFAOYSA-N 0.000 claims 2
- MSWUBXCMCDUZOT-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)Cl)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)Cl)C(OCCCC)(OCCCC)OCCCC MSWUBXCMCDUZOT-UHFFFAOYSA-N 0.000 claims 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 2
- 239000007795 chemical reaction product Substances 0.000 claims 2
- 230000001698 pyrogenic effect Effects 0.000 claims 2
- CWZQYRJRRHYJOI-UHFFFAOYSA-N 1,1,1-trimethoxydecane Chemical compound CCCCCCCCCC(OC)(OC)OC CWZQYRJRRHYJOI-UHFFFAOYSA-N 0.000 claims 1
- MZMVVHAHSRJOEO-UHFFFAOYSA-N 1-chloropropylbenzene Chemical compound CCC(Cl)C1=CC=CC=C1 MZMVVHAHSRJOEO-UHFFFAOYSA-N 0.000 claims 1
- IIEWMRPKJCXTAD-UHFFFAOYSA-N 3-(trimethoxymethyl)undecane Chemical compound C(C)C(C(OC)(OC)OC)CCCCCCCC IIEWMRPKJCXTAD-UHFFFAOYSA-N 0.000 claims 1
- SVHATDHCGHFRHG-UHFFFAOYSA-N CCCCCCCC(CCC1=CC(=CC=C1)C(C)Br)C(OC)(OC)OC Chemical compound CCCCCCCC(CCC1=CC(=CC=C1)C(C)Br)C(OC)(OC)OC SVHATDHCGHFRHG-UHFFFAOYSA-N 0.000 claims 1
- WDBACIVPJYMDLJ-UHFFFAOYSA-N CCCCCCCC(CCC1=CC(=CC=C1)C(C)Cl)C(OC)(OC)OC Chemical compound CCCCCCCC(CCC1=CC(=CC=C1)C(C)Cl)C(OC)(OC)OC WDBACIVPJYMDLJ-UHFFFAOYSA-N 0.000 claims 1
- APTRCXZYEFGFTP-UHFFFAOYSA-N CCCCCCCC(CCC1=CC(=CC=C1)CI)C(OC)(OC)OC Chemical compound CCCCCCCC(CCC1=CC(=CC=C1)CI)C(OC)(OC)OC APTRCXZYEFGFTP-UHFFFAOYSA-N 0.000 claims 1
- UOGAUENFOMISOE-UHFFFAOYSA-N CCCCCCCCC(C=CCBr)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(C=CCBr)C(OCCCC)(OCCCC)OCCCC UOGAUENFOMISOE-UHFFFAOYSA-N 0.000 claims 1
- AYFXPSNKWKPVJY-UHFFFAOYSA-N CCCCCCCCC(C=CCCl)C(C)(C)OCC Chemical compound CCCCCCCCC(C=CCCl)C(C)(C)OCC AYFXPSNKWKPVJY-UHFFFAOYSA-N 0.000 claims 1
- LVIDKOPBHZVLPM-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)C(C)I)C(OC)(OC)OC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)C(C)I)C(OC)(OC)OC LVIDKOPBHZVLPM-UHFFFAOYSA-N 0.000 claims 1
- PSDRAUCDMLPJKY-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)C(CC)Cl)C(OCCCC)(OCCCC)OCCCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)C(CC)Cl)C(OCCCC)(OCCCC)OCCCC PSDRAUCDMLPJKY-UHFFFAOYSA-N 0.000 claims 1
- DHXJMDLWGHXPGI-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)C(CC)I)C(OC)(OC)OC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)C(CC)I)C(OC)(OC)OC DHXJMDLWGHXPGI-UHFFFAOYSA-N 0.000 claims 1
- PUVKMIZEOUZMTF-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)I)C(OC)(OC)OC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C(CC)I)C(OC)(OC)OC PUVKMIZEOUZMTF-UHFFFAOYSA-N 0.000 claims 1
- NPGGNLNWNLRIST-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)CBr)C(OC)(OC)OC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)CBr)C(OC)(OC)OC NPGGNLNWNLRIST-UHFFFAOYSA-N 0.000 claims 1
- AYPYHMYEGYFBPE-UHFFFAOYSA-N ClCC1=CC=C(C=C1)CCC(C(OC)(OC)OC)CCCCCCCC Chemical compound ClCC1=CC=C(C=C1)CCC(C(OC)(OC)OC)CCCCCCCC AYPYHMYEGYFBPE-UHFFFAOYSA-N 0.000 claims 1
- HIPVTVNIGFETDW-UHFFFAOYSA-N aluminum cerium Chemical compound [Al].[Ce] HIPVTVNIGFETDW-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 abstract description 7
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract description 5
- 229930195733 hydrocarbon Natural products 0.000 abstract description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract 1
- 230000003213 activating effect Effects 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- 229910000077 silane Inorganic materials 0.000 abstract 1
- 229910052710 silicon Inorganic materials 0.000 abstract 1
- 239000010703 silicon Substances 0.000 abstract 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 21
- 238000001723 curing Methods 0.000 description 16
- 230000000052 comparative effect Effects 0.000 description 14
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 12
- 229910052799 carbon Inorganic materials 0.000 description 10
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 description 10
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 description 10
- 239000000047 product Substances 0.000 description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 8
- 239000005977 Ethylene Substances 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 238000012360 testing method Methods 0.000 description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 7
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 229910000323 aluminium silicate Inorganic materials 0.000 description 6
- 150000001721 carbon Chemical group 0.000 description 6
- 239000007822 coupling agent Substances 0.000 description 6
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000011159 matrix material Substances 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000012763 reinforcing filler Substances 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- 238000005859 coupling reaction Methods 0.000 description 5
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 5
- 229910052753 mercury Inorganic materials 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 238000010058 rubber compounding Methods 0.000 description 5
- 238000006467 substitution reaction Methods 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 4
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 4
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 4
- 238000004939 coking Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000010168 coupling process Methods 0.000 description 4
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
- 238000007720 emulsion polymerization reaction Methods 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000004848 polyfunctional curative Substances 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 238000005096 rolling process Methods 0.000 description 4
- 229910052707 ruthenium Inorganic materials 0.000 description 4
- 229960002447 thiram Drugs 0.000 description 4
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 230000008878 coupling Effects 0.000 description 3
- BFMKFCLXZSUVPI-UHFFFAOYSA-N ethyl but-3-enoate Chemical compound CCOC(=O)CC=C BFMKFCLXZSUVPI-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 125000005394 methallyl group Chemical group 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 230000002787 reinforcement Effects 0.000 description 3
- 238000005728 strengthening Methods 0.000 description 3
- 230000000930 thermomechanical effect Effects 0.000 description 3
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 3
- 125000003944 tolyl group Chemical group 0.000 description 3
- 229910052723 transition metal Inorganic materials 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CENHJCFYWRFZFC-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)C)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)C)C(OCC)(OCC)OCC CENHJCFYWRFZFC-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- FKBYELFMJHYOFH-UHFFFAOYSA-N ClCC1=CC=C(C=C1)CCC(C(OC)(OC)OC)CCCCCCC Chemical compound ClCC1=CC=C(C=C1)CCC(C(OC)(OC)OC)CCCCCCC FKBYELFMJHYOFH-UHFFFAOYSA-N 0.000 description 2
- UBVRPDPANQXXPM-UHFFFAOYSA-N ClCC=CC(C(OCC)(OCC)OCC)CCCCCCCC Chemical compound ClCC=CC(C(OCC)(OCC)OCC)CCCCCCCC UBVRPDPANQXXPM-UHFFFAOYSA-N 0.000 description 2
- 206010011416 Croup infectious Diseases 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 125000000304 alkynyl group Chemical group 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 125000006165 cyclic alkyl group Chemical group 0.000 description 2
- 150000001934 cyclohexanes Chemical group 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000012990 dithiocarbamate Substances 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- 229910001507 metal halide Inorganic materials 0.000 description 2
- 150000005309 metal halides Chemical class 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920001195 polyisoprene Polymers 0.000 description 2
- 239000005077 polysulfide Substances 0.000 description 2
- 229920001021 polysulfide Polymers 0.000 description 2
- 150000008117 polysulfides Polymers 0.000 description 2
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000001010 sulfinic acid amide group Chemical group 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 239000003039 volatile agent Substances 0.000 description 2
- VNDYJBBGRKZCSX-UHFFFAOYSA-L zinc bromide Chemical compound Br[Zn]Br VNDYJBBGRKZCSX-UHFFFAOYSA-L 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- UAYWVJHJZHQCIE-UHFFFAOYSA-L zinc iodide Chemical compound I[Zn]I UAYWVJHJZHQCIE-UHFFFAOYSA-L 0.000 description 2
- JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 description 1
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- VHSBTBDMKDUVKG-UHFFFAOYSA-N (dimethylcarbamothioyltrisulfanyl) n,n-dimethylcarbamodithioate Chemical compound CN(C)C(=S)SSSSC(=S)N(C)C VHSBTBDMKDUVKG-UHFFFAOYSA-N 0.000 description 1
- NWRZGFYWENINNX-UHFFFAOYSA-N 1,1,2-tris(ethenyl)cyclohexane Chemical compound C=CC1CCCCC1(C=C)C=C NWRZGFYWENINNX-UHFFFAOYSA-N 0.000 description 1
- GCYUJISWSVALJD-UHFFFAOYSA-N 1,1-diethylcyclohexane Chemical compound CCC1(CC)CCCCC1 GCYUJISWSVALJD-UHFFFAOYSA-N 0.000 description 1
- FPZXQVCYHDMIIA-UHFFFAOYSA-N 1,1-diphenylthiourea Chemical compound C=1C=CC=CC=1N(C(=S)N)C1=CC=CC=C1 FPZXQVCYHDMIIA-UHFFFAOYSA-N 0.000 description 1
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 1
- GMJYXQZCAGQXHT-UHFFFAOYSA-N 1,3-benzothiazole-2-sulfinamide Chemical compound C1=CC=C2SC(S(=O)N)=NC2=C1 GMJYXQZCAGQXHT-UHFFFAOYSA-N 0.000 description 1
- PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 description 1
- SLBOQBILGNEPEB-UHFFFAOYSA-N 1-chloroprop-2-enylbenzene Chemical compound C=CC(Cl)C1=CC=CC=C1 SLBOQBILGNEPEB-UHFFFAOYSA-N 0.000 description 1
- ASZMYJSJEOGSBR-UHFFFAOYSA-N 1-chlorotridecane Chemical compound CCCCCCCCCCCCCCl ASZMYJSJEOGSBR-UHFFFAOYSA-N 0.000 description 1
- LLMLGZUZTFMXSA-UHFFFAOYSA-N 2,3,4,5,6-pentachlorobenzenethiol Chemical compound SC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LLMLGZUZTFMXSA-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- WFCSWCVEJLETKA-UHFFFAOYSA-N 2-piperazin-1-ylethanol Chemical compound OCCN1CCNCC1 WFCSWCVEJLETKA-UHFFFAOYSA-N 0.000 description 1
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
- HLBZWYXLQJQBKU-UHFFFAOYSA-N 4-(morpholin-4-yldisulfanyl)morpholine Chemical compound C1COCCN1SSN1CCOCC1 HLBZWYXLQJQBKU-UHFFFAOYSA-N 0.000 description 1
- YBYVZXAEQRHBPY-UHFFFAOYSA-N 4-(morpholin-4-yltetrasulfanyl)morpholine Chemical compound C1COCCN1SSSSN1CCOCC1 YBYVZXAEQRHBPY-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- HUARFLJIYHQMBH-UHFFFAOYSA-N C(C)OC(CCCCCCCCCC(CC)SSSSC(CC)CCCCCCCCCC(OCC)(OCC)OCC)(OCC)OCC Chemical compound C(C)OC(CCCCCCCCCC(CC)SSSSC(CC)CCCCCCCCCC(OCC)(OCC)OCC)(OCC)OCC HUARFLJIYHQMBH-UHFFFAOYSA-N 0.000 description 1
- RBFOPHOQKKKNFG-UHFFFAOYSA-N CCCCCCCC(CCC1=CC=C(C=C1)C(C)Cl)C(OC)(OC)OC Chemical compound CCCCCCCC(CCC1=CC=C(C=C1)C(C)Cl)C(OC)(OC)OC RBFOPHOQKKKNFG-UHFFFAOYSA-N 0.000 description 1
- RSZWOPHGVSPPNG-UHFFFAOYSA-N CCCCCCCC(CCC1=CC=C(C=C1)CBr)C(OC)(OC)OC Chemical compound CCCCCCCC(CCC1=CC=C(C=C1)CBr)C(OC)(OC)OC RSZWOPHGVSPPNG-UHFFFAOYSA-N 0.000 description 1
- XEHDLKHVXLTDOM-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)C(CC)Br)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)C(CC)Br)C(OCC)(OCC)OCC XEHDLKHVXLTDOM-UHFFFAOYSA-N 0.000 description 1
- SEKSDZYGPNIJEZ-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC(=CC=C1)CCl)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC(=CC=C1)CCl)C(OCC)(OCC)OCC SEKSDZYGPNIJEZ-UHFFFAOYSA-N 0.000 description 1
- KZDLDQTVKAGEIE-UHFFFAOYSA-N CCCCCCCCC(CCC1=CC=C(C=C1)CI)C(OCC)(OCC)OCC Chemical compound CCCCCCCCC(CCC1=CC=C(C=C1)CI)C(OCC)(OCC)OCC KZDLDQTVKAGEIE-UHFFFAOYSA-N 0.000 description 1
- LIMQAQBQERSKBC-UHFFFAOYSA-N CCCCCCCCCC(CCC1=CC(CCl)=CC=C1)OCC Chemical compound CCCCCCCCCC(CCC1=CC(CCl)=CC=C1)OCC LIMQAQBQERSKBC-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- BWLUMTFWVZZZND-UHFFFAOYSA-N Dibenzylamine Chemical compound C=1C=CC=CC=1CNCC1=CC=CC=C1 BWLUMTFWVZZZND-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 241001441571 Hiodontidae Species 0.000 description 1
- UTGQNNCQYDRXCH-UHFFFAOYSA-N N,N'-diphenyl-1,4-phenylenediamine Chemical compound C=1C=C(NC=2C=CC=CC=2)C=CC=1NC1=CC=CC=C1 UTGQNNCQYDRXCH-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- AKSPFWBNMBOOHI-UHFFFAOYSA-N SCC=1NC=CN1.[Zn] Chemical compound SCC=1NC=CN1.[Zn] AKSPFWBNMBOOHI-UHFFFAOYSA-N 0.000 description 1
- 241000872198 Serjania polyphylla Species 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 125000004450 alkenylene group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000746 allylic group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001454 anthracenes Chemical class 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 1
- 238000009530 blood pressure measurement Methods 0.000 description 1
- 230000031709 bromination Effects 0.000 description 1
- 238000005893 bromination reaction Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- RTACIUYXLGWTAE-UHFFFAOYSA-N buta-1,3-diene;2-methylbuta-1,3-diene;styrene Chemical compound C=CC=C.CC(=C)C=C.C=CC1=CC=CC=C1 RTACIUYXLGWTAE-UHFFFAOYSA-N 0.000 description 1
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- DRVWBEJJZZTIGJ-UHFFFAOYSA-N cerium(3+);oxygen(2-) Chemical class [O-2].[O-2].[O-2].[Ce+3].[Ce+3] DRVWBEJJZZTIGJ-UHFFFAOYSA-N 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229960001701 chloroform Drugs 0.000 description 1
- 229920003211 cis-1,4-polyisoprene Polymers 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 230000001808 coupling effect Effects 0.000 description 1
- ZOLLIQAKMYWTBR-RYMQXAEESA-N cyclododecatriene Chemical compound C/1C\C=C\CC\C=C/CC\C=C\1 ZOLLIQAKMYWTBR-RYMQXAEESA-N 0.000 description 1
- HYPABJGVBDSCIT-UPHRSURJSA-N cyclododecene Chemical compound C1CCCCC\C=C/CCCC1 HYPABJGVBDSCIT-UPHRSURJSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000006612 decyloxy group Chemical group 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- AFZSMODLJJCVPP-UHFFFAOYSA-N dibenzothiazol-2-yl disulfide Chemical compound C1=CC=C2SC(SSC=3SC4=CC=CC=C4N=3)=NC2=C1 AFZSMODLJJCVPP-UHFFFAOYSA-N 0.000 description 1
- 229920003244 diene elastomer Polymers 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- GPAYUJZHTULNBE-UHFFFAOYSA-O diphenylphosphanium Chemical compound C=1C=CC=CC=1[PH2+]C1=CC=CC=C1 GPAYUJZHTULNBE-UHFFFAOYSA-O 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001493 electron microscopy Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical group [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 150000002780 morpholines Chemical class 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- IUJLOAKJZQBENM-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)-2-methylpropan-2-amine Chemical compound C1=CC=C2SC(SNC(C)(C)C)=NC2=C1 IUJLOAKJZQBENM-UHFFFAOYSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- WGARMULIELDQEH-UHFFFAOYSA-N n-cyclohexyl-1,3-benzothiazole-2-sulfinamide Chemical compound N=1C2=CC=CC=C2SC=1S(=O)NC1CCCCC1 WGARMULIELDQEH-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- 239000013500 performance material Substances 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000002459 porosimetry Methods 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- LJZPPWWHKPGCHS-UHFFFAOYSA-N propargyl chloride Chemical compound ClCC#C LJZPPWWHKPGCHS-UHFFFAOYSA-N 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- LZOZLBFZGFLFBV-UHFFFAOYSA-N sulfene Chemical compound C=S(=O)=O LZOZLBFZGFLFBV-UHFFFAOYSA-N 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- WNDHBMUTTTWRJA-UHFFFAOYSA-N tetrahydridosulfur Chemical compound [SH4] WNDHBMUTTTWRJA-UHFFFAOYSA-N 0.000 description 1
- LPSXSORODABQKT-UHFFFAOYSA-N tetrahydrodicyclopentadiene Chemical compound C1C2CCC1C1C2CCC1 LPSXSORODABQKT-UHFFFAOYSA-N 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 150000003585 thioureas Chemical class 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
- UBZYKBZMAMTNKW-UHFFFAOYSA-J titanium tetrabromide Chemical compound Br[Ti](Br)(Br)Br UBZYKBZMAMTNKW-UHFFFAOYSA-J 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
- 229940102001 zinc bromide Drugs 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- NEYNBSGIXOOZGZ-UHFFFAOYSA-L zinc;butoxymethanedithioate Chemical compound [Zn+2].CCCCOC([S-])=S.CCCCOC([S-])=S NEYNBSGIXOOZGZ-UHFFFAOYSA-L 0.000 description 1
- MBBWTVUFIXOUBE-UHFFFAOYSA-L zinc;dicarbamodithioate Chemical compound [Zn+2].NC([S-])=S.NC([S-])=S MBBWTVUFIXOUBE-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- 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
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/5406—Silicon-containing compounds containing elements other than oxygen or nitrogen
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/548—Silicon-containing compounds containing sulfur
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/703,969 US7625965B2 (en) | 2007-02-08 | 2007-02-08 | Rubber composition, process of preparing same and articles made therefrom |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW200904875A TW200904875A (en) | 2009-02-01 |
| TWI441858B true TWI441858B (zh) | 2014-06-21 |
Family
ID=39563341
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW097104334A TWI441858B (zh) | 2007-02-08 | 2008-02-04 | 橡膠組成物,彼之製法及由彼製得之物件 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7625965B2 (enExample) |
| EP (1) | EP2121349B1 (enExample) |
| JP (1) | JP5593073B2 (enExample) |
| CN (2) | CN102432924B (enExample) |
| AT (1) | ATE488381T1 (enExample) |
| DE (1) | DE602008003526D1 (enExample) |
| PL (1) | PL2121349T3 (enExample) |
| TW (1) | TWI441858B (enExample) |
| WO (1) | WO2008097587A1 (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7816435B2 (en) * | 2007-10-31 | 2010-10-19 | Momentive Performance Materials Inc. | Halo-functional silane, process for its preparation, rubber composition containing same and articles manufactured therefrom |
| US8143336B2 (en) * | 2008-08-07 | 2012-03-27 | Momentive Performance Materials Inc. | Activated halo-containing aralkylsilane composition, process of preparing same and rubber compositions made therefrom |
| ATE536388T1 (de) * | 2009-08-07 | 2011-12-15 | Rhein Chemie Rheinau Gmbh | Vulkanisationsbeschleunigende mischung |
| US8846806B2 (en) * | 2011-09-23 | 2014-09-30 | Ppg Industries Ohio, Inc. | Treated fillers, compositions containing same, and articles prepared therefrom |
| ITTO20111208A1 (it) * | 2011-12-23 | 2013-06-24 | Bridgestone Corp | Mescola di gomma per pneumatici |
| RU2487893C1 (ru) * | 2011-12-26 | 2013-07-20 | Виктор Александрович Стариков | Резиновая смесь для изготовления пористых изделий |
| CN102675697B (zh) * | 2012-06-21 | 2014-03-12 | 三角轮胎股份有限公司 | 抗硫化返原的胎肩垫胶橡胶组合物 |
| FR3038902B1 (fr) * | 2015-07-15 | 2022-03-11 | Cabot Corp | Composite en elastomere renforce avec de la silice et produits en contenant |
| BR112018000833B1 (pt) | 2015-07-15 | 2022-12-13 | Cabot Corporation | Métodos de produção de compósito de elastômero reforçado com sílica e artigo contendo o mesmo |
| CN105131380A (zh) * | 2015-08-18 | 2015-12-09 | 合肥市再德高分子材料有限公司 | 一种高性能改性羧基丁腈橡胶复合材料 |
| DE102015223246A1 (de) * | 2015-11-24 | 2017-05-24 | Wacker Chemie Ag | Organocopolymer-Dispersionen |
| WO2018128141A1 (ja) * | 2017-01-06 | 2018-07-12 | 住友ゴム工業株式会社 | 加硫後ゴム組成物及び空気入りタイヤ |
| DE102017221232A1 (de) * | 2017-11-28 | 2019-05-29 | Continental Reifen Deutschland Gmbh | Schwefelvernetzbare Kautschukmischung, Vulkanisat der Kautschukmischung und Fahrzeugreifen |
| EP3650246B1 (de) | 2018-11-12 | 2025-01-08 | Continental Reifen Deutschland GmbH | Schwefelvernetzbare kautschukmischung, vulkanisat und fahrzeugreifen |
| EP3650245B1 (de) | 2018-11-12 | 2023-08-30 | Continental Reifen Deutschland GmbH | Schwefelvernetzbare kautschukmischung, vulkanisat und fahrzeugreifen |
| KR102767054B1 (ko) | 2019-06-05 | 2025-02-14 | 비욘드 로투스 엘엘씨 | 타이어 트레드 |
| JP7331566B2 (ja) * | 2019-09-06 | 2023-08-23 | 住友ゴム工業株式会社 | タイヤ部材の物性予測方法 |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3692812A (en) * | 1971-04-21 | 1972-09-19 | Gen Electric | Method of producing alkoxy-substituted mercaptoalkyl silanes |
| GB1435894A (en) * | 1972-07-21 | 1976-05-19 | Ici Ltd | Production of isocyanates |
| DE2819638C3 (de) * | 1978-05-05 | 1986-11-13 | Degussa Ag, 6000 Frankfurt | Vulkanisierbare Halogenkautschuk-Mischungen |
| DE2933346C2 (de) * | 1979-08-17 | 1982-07-01 | Degussa Ag, 6000 Frankfurt | Silan/Füllstoff-Präparationen, Verfahren zu deren Herstellung und Anwendung derselben |
| JP2630596B2 (ja) | 1987-07-27 | 1997-07-16 | 株式会社ブリヂストン | シランカップリング剤 |
| DE4004781A1 (de) * | 1990-02-16 | 1991-08-22 | Degussa | Verfahren zur herstellung von mit organosiliciumverbindungen modifizierten fuellstoffen, die so hergestellten fuellstoffe und deren verwendung |
| US5268439A (en) * | 1991-01-02 | 1993-12-07 | Bridgestone/Firestone, Inc. | Tin containing elastomers and products having reduced hysteresis properties |
| CA2105719A1 (en) | 1993-06-28 | 1994-12-29 | Rene Jean Zimmer | Silica based aggregates, elastomers reinforced therewith and tire with tread thereof |
| JP3382322B2 (ja) * | 1993-11-09 | 2003-03-04 | 住友ゴム工業株式会社 | 車両用タイヤ |
| IT1274257B (it) * | 1995-02-24 | 1997-07-15 | Pirelli | Procedimento per la produzione di una mescola di gomma vulcanizzabile con carica rinforzante a base di silice |
| DE69632862T2 (de) * | 1995-08-16 | 2005-07-14 | General Electric Co. | Stabile Silanzusammensetzungen auf Silikatträger |
| EP0767206B1 (fr) * | 1995-10-04 | 2002-07-10 | Compagnie Generale Des Etablissements Michelin-Michelin & Cie | Composition de caoutchouc à base d'un polymère diénique comprenant un dérivé organosilane, utilisable pour la fabrication de bandes de roulement de pneumatiques |
| WO1999031178A1 (en) * | 1997-12-15 | 1999-06-24 | Exxon Chemical Patents Inc. | Transparent and colorable elastomeric compositions |
| JP4861587B2 (ja) | 1999-12-30 | 2012-01-25 | ソシエテ ド テクノロジー ミシュラン | 熱誘発性ラジカル開始剤によって活性化されるカップリング剤(白色充填剤/ジエンエラストマー)を含むタイヤ用ゴム組成物 |
| HUP0302341A2 (hu) * | 2000-06-13 | 2003-10-28 | Exxonmobil Chemical Patents Inc. | Eljárás szilícium-dioxiddal töltött elasztomer-készítmények előállítására |
| DE60127980T2 (de) | 2000-09-15 | 2008-01-17 | Société de Technologie Michelin | Kautschukzusammensetzung für reifen die als kupplungsmittel ein citraconimidoalkoxysilan enthält |
| US20040014869A1 (en) * | 2001-05-09 | 2004-01-22 | Wong Wai Keung | Method for preparing silica filled elastomeric compositions |
| WO2004024813A1 (fr) | 2002-09-10 | 2004-03-25 | Societe De Technologie Michelin | Composition de caoutchouc pour bande de roulement de pneumatique |
| US6706398B1 (en) * | 2002-09-13 | 2004-03-16 | Dow Corning Corporation | Organosilicon compounds and blends for treating silica |
| US6811823B2 (en) * | 2002-09-13 | 2004-11-02 | Dow Corning Corporation | Hydrophobing silica with organosilicon compounds and blends thereof |
| KR100629684B1 (ko) | 2003-01-23 | 2006-09-29 | 전남대학교산학협력단 | 둥지 실리카를 포함하는 고무조성물 |
| JP2005232445A (ja) | 2004-01-23 | 2005-09-02 | Daiso Co Ltd | ゴム用添加剤およびそれを用いたゴム組成物 |
| US20060025506A1 (en) * | 2004-07-30 | 2006-02-02 | Weller Keith J | Silane compositions, processes for their preparation and rubber compositions containing same |
-
2007
- 2007-02-08 US US11/703,969 patent/US7625965B2/en active Active
-
2008
- 2008-02-04 TW TW097104334A patent/TWI441858B/zh not_active IP Right Cessation
- 2008-02-06 DE DE602008003526T patent/DE602008003526D1/de active Active
- 2008-02-06 PL PL08725244T patent/PL2121349T3/pl unknown
- 2008-02-06 CN CN201110259015.6A patent/CN102432924B/zh not_active Expired - Fee Related
- 2008-02-06 WO PCT/US2008/001587 patent/WO2008097587A1/en not_active Ceased
- 2008-02-06 AT AT08725244T patent/ATE488381T1/de not_active IP Right Cessation
- 2008-02-06 CN CN200880009764XA patent/CN101641226B/zh not_active Expired - Fee Related
- 2008-02-06 EP EP08725244A patent/EP2121349B1/en not_active Not-in-force
- 2008-02-06 JP JP2009549096A patent/JP5593073B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| TW200904875A (en) | 2009-02-01 |
| CN101641226A (zh) | 2010-02-03 |
| US7625965B2 (en) | 2009-12-01 |
| CN102432924B (zh) | 2014-04-09 |
| CN101641226B (zh) | 2013-02-13 |
| ATE488381T1 (de) | 2010-12-15 |
| JP5593073B2 (ja) | 2014-09-17 |
| HK1140729A1 (en) | 2010-10-22 |
| US20080194746A1 (en) | 2008-08-14 |
| EP2121349B1 (en) | 2010-11-17 |
| PL2121349T3 (pl) | 2011-06-30 |
| CN102432924A (zh) | 2012-05-02 |
| JP2010518229A (ja) | 2010-05-27 |
| EP2121349A1 (en) | 2009-11-25 |
| DE602008003526D1 (de) | 2010-12-30 |
| WO2008097587A1 (en) | 2008-08-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TWI441858B (zh) | 橡膠組成物,彼之製法及由彼製得之物件 | |
| JP5450093B2 (ja) | シリル化コアポリスルフィドを含有するタイヤ組成物および部品 | |
| JP5603771B2 (ja) | ゴム組成物の調製プロセスならびにそれらから作製される製品 | |
| KR101659967B1 (ko) | 황-함유 고리형 지방족 화합물, 황-함유 고리형 지방족 화합물을 포함하는 충전 황-가황성 엘라스토머 조성물 및 그로부터 제조된 물품들 | |
| EP2099857B1 (en) | Tire compositions and components containing free-flowing filler compositions | |
| CA2430251C (en) | Mineral-filled elastomer compositions | |
| JP6018358B2 (ja) | 自由流動性充填剤組成物およびそれを含有するラバー組成物 | |
| JP5514546B2 (ja) | メルカプト官能性シランおよびその調製のプロセス | |
| US7169872B2 (en) | Hybrid silicon-containing coupling agents for filled elastomer compositions | |
| JP5940765B2 (ja) | ハロ官能性シラン、その調製プロセス、それを含むゴム組成物およびそれらから製造される製品 | |
| BRPI0720723B1 (pt) | polissulfeto de núcleo silado, composição de borracha e processo para fabricar um polissulfeto de núcleo silado | |
| JP5649821B2 (ja) | メルカプト官能性シランを含む弾性体組成物およびその作製のプロセス | |
| JP5735421B2 (ja) | 活性化ハロ含有アラルキルシラン | |
| HK1140729B (en) | Rubber composition, process of preparing same and articles made therefrom |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Annulment or lapse of patent due to non-payment of fees |