CN1073460A - 稳定剂混合物 - Google Patents
稳定剂混合物 Download PDFInfo
- Publication number
- CN1073460A CN1073460A CN92114141A CN92114141A CN1073460A CN 1073460 A CN1073460 A CN 1073460A CN 92114141 A CN92114141 A CN 92114141A CN 92114141 A CN92114141 A CN 92114141A CN 1073460 A CN1073460 A CN 1073460A
- Authority
- CN
- China
- Prior art keywords
- alkyl
- carbon atom
- butyl
- hydrogen
- stabilizer blend
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 66
- 239000003381 stabilizer Substances 0.000 title claims abstract description 33
- -1 fatty acid ester epoxide Chemical class 0.000 claims abstract description 62
- 229920005989 resin Polymers 0.000 claims abstract description 36
- 239000011347 resin Substances 0.000 claims abstract description 36
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 35
- 239000002253 acid Substances 0.000 claims abstract description 7
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 5
- 239000000194 fatty acid Substances 0.000 claims abstract description 5
- 229930195729 fatty acid Natural products 0.000 claims abstract description 5
- 150000002632 lipids Chemical class 0.000 claims abstract description 5
- 102000004377 Thiopurine S-methyltransferases Human genes 0.000 claims abstract description 4
- 108090000958 Thiopurine S-methyltransferases Proteins 0.000 claims abstract description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- 125000004432 carbon atom Chemical group C* 0.000 claims description 20
- 239000001257 hydrogen Substances 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 229910052799 carbon Inorganic materials 0.000 claims description 18
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 9
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 9
- 229920001577 copolymer Polymers 0.000 claims description 7
- VSKJLJHPAFKHBX-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 VSKJLJHPAFKHBX-UHFFFAOYSA-N 0.000 claims description 6
- 239000013032 Hydrocarbon resin Substances 0.000 claims description 6
- 229920006270 hydrocarbon resin Polymers 0.000 claims description 6
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 5
- 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 claims description 5
- 235000012424 soybean oil Nutrition 0.000 claims description 5
- 239000003549 soybean oil Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 125000005907 alkyl ester group Chemical group 0.000 claims description 2
- 150000002118 epoxides Chemical class 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 description 25
- 229960003742 phenol Drugs 0.000 description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 17
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 13
- 150000002148 esters Chemical class 0.000 description 13
- 239000002585 base Substances 0.000 description 11
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 9
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 8
- IYXGSMUGOJNHAZ-UHFFFAOYSA-N Ethyl malonate Chemical compound CCOC(=O)CC(=O)OCC IYXGSMUGOJNHAZ-UHFFFAOYSA-N 0.000 description 7
- 229940059574 pentaerithrityl Drugs 0.000 description 7
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- 150000001721 carbon Chemical group 0.000 description 6
- FTWUXYZHDFCGSV-UHFFFAOYSA-N n,n'-diphenyloxamide Chemical compound C=1C=CC=CC=1NC(=O)C(=O)NC1=CC=CC=C1 FTWUXYZHDFCGSV-UHFFFAOYSA-N 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 235000019198 oils Nutrition 0.000 description 6
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 6
- 239000007859 condensation product Substances 0.000 description 5
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 5
- 150000002924 oxiranes Chemical class 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 230000006641 stabilisation Effects 0.000 description 5
- 238000011105 stabilization Methods 0.000 description 5
- 229920002554 vinyl polymer Polymers 0.000 description 5
- PMNGNPRHPYYVNM-UHFFFAOYSA-N 1-hydroxyundecane-3-sulfonic acid Chemical compound CCCCCCCCC(CCO)S(O)(=O)=O PMNGNPRHPYYVNM-UHFFFAOYSA-N 0.000 description 4
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 4
- GLDQAMYCGOIJDV-UHFFFAOYSA-N 2,3-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=CC(O)=C1O GLDQAMYCGOIJDV-UHFFFAOYSA-N 0.000 description 4
- IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- ICHKVCYUNCKCGL-UHFFFAOYSA-N CN(C)C.OCCCCCCO Chemical compound CN(C)C.OCCCCCCO ICHKVCYUNCKCGL-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- YZZRPVXYOXHDNH-UHFFFAOYSA-N NN.OCCOC(C(=O)O)=O Chemical compound NN.OCCOC(C(=O)O)=O YZZRPVXYOXHDNH-UHFFFAOYSA-N 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 4
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical group CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 4
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- GXURZKWLMYOCDX-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;dihydroxyphosphanyl dihydrogen phosphite Chemical class OP(O)OP(O)O.OCC(CO)(CO)CO GXURZKWLMYOCDX-UHFFFAOYSA-N 0.000 description 3
- LCANECIWPMDASZ-UHFFFAOYSA-N 2-isocyanatoethanol Chemical compound OCCN=C=O LCANECIWPMDASZ-UHFFFAOYSA-N 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000004831 Hot glue Substances 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000005660 chlorination reaction Methods 0.000 description 3
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 3
- 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 3
- 230000032050 esterification Effects 0.000 description 3
- 238000005886 esterification reaction Methods 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 150000000182 1,3,5-triazines Chemical class 0.000 description 2
- YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical compound C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- ZEMPKEQAKRGZGQ-AAKVHIHISA-N 2,3-bis[[(z)-12-hydroxyoctadec-9-enoyl]oxy]propyl (z)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCCC(O)C\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CC(O)CCCCCC)COC(=O)CCCCCCC\C=C/CC(O)CCCCCC ZEMPKEQAKRGZGQ-AAKVHIHISA-N 0.000 description 2
- SLUKQUGVTITNSY-UHFFFAOYSA-N 2,6-di-tert-butyl-4-methoxyphenol Chemical compound COC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SLUKQUGVTITNSY-UHFFFAOYSA-N 0.000 description 2
- IKEHOXWJQXIQAG-UHFFFAOYSA-N 2-tert-butyl-4-methylphenol Chemical compound CC1=CC=C(O)C(C(C)(C)C)=C1 IKEHOXWJQXIQAG-UHFFFAOYSA-N 0.000 description 2
- BKZXZGWHTRCFPX-UHFFFAOYSA-N 2-tert-butyl-6-methylphenol Chemical compound CC1=CC=CC(C(C)(C)C)=C1O BKZXZGWHTRCFPX-UHFFFAOYSA-N 0.000 description 2
- KMWIPXLIKIAZMT-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanehydrazide Chemical compound CC(C)(C)C1=CC(CCC(=O)NN)=CC(C(C)(C)C)=C1O KMWIPXLIKIAZMT-UHFFFAOYSA-N 0.000 description 2
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 2
- MSGFMKMFGGXSTO-UHFFFAOYSA-N C(C)(C)(C)C=1C=C(C(=CC1O)CN)CCCC Chemical compound C(C)(C)(C)C=1C=C(C(=CC1O)CN)CCCC MSGFMKMFGGXSTO-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 239000004902 Softening Agent Substances 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- OUUQCZGPVNCOIJ-UHFFFAOYSA-M Superoxide Chemical compound [O-][O] OUUQCZGPVNCOIJ-UHFFFAOYSA-M 0.000 description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 230000002152 alkylating effect Effects 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- CCRCUPLGCSFEDV-UHFFFAOYSA-N cinnamic acid methyl ester Natural products COC(=O)C=CC1=CC=CC=C1 CCRCUPLGCSFEDV-UHFFFAOYSA-N 0.000 description 2
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 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 2
- LOEUCBBZEHMJQN-UHFFFAOYSA-N hydrazine;oxalic acid Chemical compound NN.OC(=O)C(O)=O LOEUCBBZEHMJQN-UHFFFAOYSA-N 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000006078 metal deactivator Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 125000001421 myristyl 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])[H] 0.000 description 2
- ODGYWRBCQWKSSH-UHFFFAOYSA-N n'-ethylpropane-1,3-diamine Chemical compound CCNCCCN ODGYWRBCQWKSSH-UHFFFAOYSA-N 0.000 description 2
- 235000006408 oxalic acid Nutrition 0.000 description 2
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
- 229920001197 polyacetylene Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 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 2
- 238000003756 stirring Methods 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- BJGZXKKYBXZLAM-UHFFFAOYSA-N (2,4-ditert-butyl-6-methylphenyl) 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CC1=CC(C(C)(C)C)=CC(C(C)(C)C)=C1OC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 BJGZXKKYBXZLAM-UHFFFAOYSA-N 0.000 description 1
- HQEPZWYPQQKFLU-UHFFFAOYSA-N (2,6-dihydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC(O)=C1C(=O)C1=CC=CC=C1 HQEPZWYPQQKFLU-UHFFFAOYSA-N 0.000 description 1
- FKFOHTUAFNQANW-UHFFFAOYSA-N (3,5-ditert-butyl-4-hydroxyphenyl) octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 FKFOHTUAFNQANW-UHFFFAOYSA-N 0.000 description 1
- ZEBMSMUPGIOANU-UHFFFAOYSA-N (3,5-ditert-butyl-4-hydroxyphenyl)methylphosphonic acid Chemical compound CC(C)(C)C1=CC(CP(O)(O)=O)=CC(C(C)(C)C)=C1O ZEBMSMUPGIOANU-UHFFFAOYSA-N 0.000 description 1
- ZIJHTQPOUJBOHK-UHFFFAOYSA-N (3-tert-butyl-4-hydroxy-5-methylphenyl)methylphosphonic acid Chemical class CC1=CC(CP(O)(O)=O)=CC(C(C)(C)C)=C1O ZIJHTQPOUJBOHK-UHFFFAOYSA-N 0.000 description 1
- GOZHNJTXLALKRL-UHFFFAOYSA-N (5-benzoyl-2,4-dihydroxyphenyl)-phenylmethanone Chemical compound OC1=CC(O)=C(C(=O)C=2C=CC=CC=2)C=C1C(=O)C1=CC=CC=C1 GOZHNJTXLALKRL-UHFFFAOYSA-N 0.000 description 1
- OJOWICOBYCXEKR-KRXBUXKQSA-N (5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C/C)/CC1C=C2 OJOWICOBYCXEKR-KRXBUXKQSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- JEFSTMHERNSDBC-UHFFFAOYSA-N 1,2-dimethylcyclohexa-2,4-dien-1-ol Chemical compound CC1=CC=CCC1(C)O JEFSTMHERNSDBC-UHFFFAOYSA-N 0.000 description 1
- ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 1
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
- LRTOHSLOFCWHRF-UHFFFAOYSA-N 1-methyl-1h-indene Chemical compound C1=CC=C2C(C)C=CC2=C1 LRTOHSLOFCWHRF-UHFFFAOYSA-N 0.000 description 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 1
- STHGLRYNMROMHZ-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)-11-methyl-3-(8-methylnonyl)dodecane-1,3-diol Chemical compound C(CCCCCCC(C)C)C(O)(C(CO)(CO)CO)CCCCCCCC(C)C STHGLRYNMROMHZ-UHFFFAOYSA-N 0.000 description 1
- OCSIKZYSDOXRPA-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)-3-octadecylhenicosane-1,3-diol dihydroxyphosphanyl dihydrogen phosphite Chemical class OP(O)OP(O)O.C(CCCCCCCCCCCCCCCCC)C(O)(C(CO)(CO)CO)CCCCCCCCCCCCCCCCCC OCSIKZYSDOXRPA-UHFFFAOYSA-N 0.000 description 1
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 1
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
- OPLCSTZDXXUYDU-UHFFFAOYSA-N 2,4-dimethyl-6-tert-butylphenol Chemical compound CC1=CC(C)=C(O)C(C(C)(C)C)=C1 OPLCSTZDXXUYDU-UHFFFAOYSA-N 0.000 description 1
- FLLRQABPKFCXSO-UHFFFAOYSA-N 2,5-ditert-butyl-4-methoxyphenol Chemical compound COC1=CC(C(C)(C)C)=C(O)C=C1C(C)(C)C FLLRQABPKFCXSO-UHFFFAOYSA-N 0.000 description 1
- BVUXDWXKPROUDO-UHFFFAOYSA-N 2,6-di-tert-butyl-4-ethylphenol Chemical compound CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 BVUXDWXKPROUDO-UHFFFAOYSA-N 0.000 description 1
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
- JBYWTKPHBLYYFJ-UHFFFAOYSA-N 2,6-ditert-butyl-4-(2-methylpropyl)phenol Chemical compound CC(C)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 JBYWTKPHBLYYFJ-UHFFFAOYSA-N 0.000 description 1
- SCXYLTWTWUGEAA-UHFFFAOYSA-N 2,6-ditert-butyl-4-(methoxymethyl)phenol Chemical compound COCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SCXYLTWTWUGEAA-UHFFFAOYSA-N 0.000 description 1
- STHGHFNAPPFPQV-UHFFFAOYSA-N 2,6-ditert-butyl-4-propylphenol Chemical compound CCCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 STHGHFNAPPFPQV-UHFFFAOYSA-N 0.000 description 1
- HHPDFYDITNAMAM-UHFFFAOYSA-N 2-[cyclohexyl(2-hydroxyethyl)amino]ethanol Chemical compound OCCN(CCO)C1CCCCC1 HHPDFYDITNAMAM-UHFFFAOYSA-N 0.000 description 1
- UIXRDRQSWYSVNK-UHFFFAOYSA-N 2-butyl-4,6-dimethylphenol Chemical compound CCCCC1=CC(C)=CC(C)=C1O UIXRDRQSWYSVNK-UHFFFAOYSA-N 0.000 description 1
- GTLMTHAWEBRMGI-UHFFFAOYSA-N 2-cyclohexyl-4-methylphenol Chemical compound CC1=CC=C(O)C(C2CCCCC2)=C1 GTLMTHAWEBRMGI-UHFFFAOYSA-N 0.000 description 1
- XSXYESVZDBAKKT-UHFFFAOYSA-N 2-hydroxybenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1O XSXYESVZDBAKKT-UHFFFAOYSA-N 0.000 description 1
- WBJWXIQDBDZMAW-UHFFFAOYSA-N 2-hydroxynaphthalene-1-carbonyl chloride Chemical compound C1=CC=CC2=C(C(Cl)=O)C(O)=CC=C21 WBJWXIQDBDZMAW-UHFFFAOYSA-N 0.000 description 1
- DHKGWJHJJZJZGD-UHFFFAOYSA-N 2-tert-butyl-4-(2-methylpropyl)phenol Chemical compound CC(C)CC1=CC=C(O)C(C(C)(C)C)=C1 DHKGWJHJJZJZGD-UHFFFAOYSA-N 0.000 description 1
- LZHCVNIARUXHAL-UHFFFAOYSA-N 2-tert-butyl-4-ethylphenol Chemical compound CCC1=CC=C(O)C(C(C)(C)C)=C1 LZHCVNIARUXHAL-UHFFFAOYSA-N 0.000 description 1
- XOUQAVYLRNOXDO-UHFFFAOYSA-N 2-tert-butyl-5-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- ODJQKYXPKWQWNK-UHFFFAOYSA-L 3-(2-carboxylatoethylsulfanyl)propanoate Chemical compound [O-]C(=O)CCSCCC([O-])=O ODJQKYXPKWQWNK-UHFFFAOYSA-L 0.000 description 1
- DBHUTHZPCWZNRW-UHFFFAOYSA-N 3-(3,5-dicyclohexyl-4-hydroxyphenyl)propanoic acid Chemical compound OC=1C(C2CCCCC2)=CC(CCC(=O)O)=CC=1C1CCCCC1 DBHUTHZPCWZNRW-UHFFFAOYSA-N 0.000 description 1
- IXJBDUOQGVACEL-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)-1-(1,3,5-triazinan-1-yl)propan-1-one Chemical class CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)N2CNCNC2)=C1 IXJBDUOQGVACEL-UHFFFAOYSA-N 0.000 description 1
- WPMYUUITDBHVQZ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoic acid Chemical compound CC(C)(C)C1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-N 0.000 description 1
- BCZQMWDTKGBZFG-UHFFFAOYSA-N 4-[(4-hydroxy-2,6-dimethylphenyl)disulfanyl]-3,5-dimethylphenol Chemical compound CC1=CC(O)=CC(C)=C1SSC1=C(C)C=C(O)C=C1C BCZQMWDTKGBZFG-UHFFFAOYSA-N 0.000 description 1
- WTWGHNZAQVTLSQ-UHFFFAOYSA-N 4-butyl-2,6-ditert-butylphenol Chemical compound CCCCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 WTWGHNZAQVTLSQ-UHFFFAOYSA-N 0.000 description 1
- UZNDHCZORMBARB-UHFFFAOYSA-N 4-hydroxylauric acid Chemical compound CCCCCCCCC(O)CCC(O)=O UZNDHCZORMBARB-UHFFFAOYSA-N 0.000 description 1
- UXMKUNDWNZNECH-UHFFFAOYSA-N 4-methyl-2,6-di(nonyl)phenol Chemical compound CCCCCCCCCC1=CC(C)=CC(CCCCCCCCC)=C1O UXMKUNDWNZNECH-UHFFFAOYSA-N 0.000 description 1
- OILMLWAZYNVPMG-UHFFFAOYSA-N 4-methyl-2-nonylphenol Chemical compound CCCCCCCCCC1=CC(C)=CC=C1O OILMLWAZYNVPMG-UHFFFAOYSA-N 0.000 description 1
- NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 1
- MYPXYQMABPTFFN-UHFFFAOYSA-N 4-phenoxybenzenesulfonic acid Chemical compound C1=CC(S(=O)(=O)O)=CC=C1OC1=CC=CC=C1 MYPXYQMABPTFFN-UHFFFAOYSA-N 0.000 description 1
- PTGSBGNWKPICPM-UHFFFAOYSA-N 5-octoxy-2-(1,3,5-triazin-2-yl)phenol Chemical class OC1=CC(OCCCCCCCC)=CC=C1C1=NC=NC=N1 PTGSBGNWKPICPM-UHFFFAOYSA-N 0.000 description 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- HMLGJOYZDNVPID-UHFFFAOYSA-N C(C)(C)(C)C1=C(C(=CC(=C1)CN)C(C)(C)C)C(O)C(CO)(CO)CO Chemical compound C(C)(C)(C)C1=C(C(=CC(=C1)CN)C(C)(C)C)C(O)C(CO)(CO)CO HMLGJOYZDNVPID-UHFFFAOYSA-N 0.000 description 1
- KYGSBSWBGHALLC-UHFFFAOYSA-N C(C)(C)(C)C=1C(=CC(=C(C1)C(CC(C)CCCCCCCCCCCC)S)CN)O Chemical compound C(C)(C)(C)C=1C(=CC(=C(C1)C(CC(C)CCCCCCCCCCCC)S)CN)O KYGSBSWBGHALLC-UHFFFAOYSA-N 0.000 description 1
- IPNDBXDADRHKEB-UHFFFAOYSA-N C(C)(C)(C)C=1C(=CC(=C(C1)C(CCCCCCCCCCCCCCC)S)CN)O Chemical compound C(C)(C)(C)C=1C(=CC(=C(C1)C(CCCCCCCCCCCCCCC)S)CN)O IPNDBXDADRHKEB-UHFFFAOYSA-N 0.000 description 1
- CPUMIQKFVWMTKY-UHFFFAOYSA-N C(C)(C)(C)C=1C(=CC(=C(C1)CCCCC)CN)O Chemical compound C(C)(C)(C)C=1C(=CC(=C(C1)CCCCC)CN)O CPUMIQKFVWMTKY-UHFFFAOYSA-N 0.000 description 1
- RTJUWEUCUSQYAV-UHFFFAOYSA-N C(C)(C)(C)C=1C=C(C=C(C1O)CN)CCC(=O)O Chemical compound C(C)(C)(C)C=1C=C(C=C(C1O)CN)CCC(=O)O RTJUWEUCUSQYAV-UHFFFAOYSA-N 0.000 description 1
- PPHYOXAZBPERTE-UHFFFAOYSA-N C(CCCCCCC)C1=C(C(=CC(=C1CS(=O)(=O)O)CCCCCCCC)CC)O Chemical compound C(CCCCCCC)C1=C(C(=CC(=C1CS(=O)(=O)O)CCCCCCCC)CC)O PPHYOXAZBPERTE-UHFFFAOYSA-N 0.000 description 1
- IQFIXQDCEUPUKR-UHFFFAOYSA-N C(CCCCCCC)C1=C(C(=CC(=C1O)C)CCCCCCCC)CS(=O)(=O)O Chemical compound C(CCCCCCC)C1=C(C(=CC(=C1O)C)CCCCCCCC)CS(=O)(=O)O IQFIXQDCEUPUKR-UHFFFAOYSA-N 0.000 description 1
- YHOKOCFZNYBCKX-UHFFFAOYSA-N C(CCCCCCCCCCC)P(O)(O)O Chemical class C(CCCCCCCCCCC)P(O)(O)O YHOKOCFZNYBCKX-UHFFFAOYSA-N 0.000 description 1
- DJRCMVCFUPOPKC-UHFFFAOYSA-N CCCCCCCCCCCC(=NO)C1=CC=C(C)C=C1O Chemical compound CCCCCCCCCCCC(=NO)C1=CC=C(C)C=C1O DJRCMVCFUPOPKC-UHFFFAOYSA-N 0.000 description 1
- FPVPDSGTVXBUBG-UHFFFAOYSA-N CCCCCCCCCC[O] Chemical compound CCCCCCCCCC[O] FPVPDSGTVXBUBG-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920004939 Cariflex™ Polymers 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- VSRRGPPFTIJBJG-UHFFFAOYSA-N DL-4-hydroxy stearic acid Chemical compound CCCCCCCCCCCCCCC(O)CCC(O)=O VSRRGPPFTIJBJG-UHFFFAOYSA-N 0.000 description 1
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- WZKXGVXFYDVCQP-UHFFFAOYSA-N NC(S)=S.CCCC[Ni]CCCC Chemical compound NC(S)=S.CCCC[Ni]CCCC WZKXGVXFYDVCQP-UHFFFAOYSA-N 0.000 description 1
- IWGBGUINMSOOKP-UHFFFAOYSA-N OC1=C(C(=O)CCCCCCCCCCC)C=NN1C1=CC=CC=C1 Chemical class OC1=C(C(=O)CCCCCCCCCCC)C=NN1C1=CC=CC=C1 IWGBGUINMSOOKP-UHFFFAOYSA-N 0.000 description 1
- PLYGVHXICXLDQL-UHFFFAOYSA-N OP(O)OP(O)O.C(C)(C)(C)C1=C(C(=CC(=C1)C(C)(C)C)CN)C(O)C(CO)(CO)CO Chemical class OP(O)OP(O)O.C(C)(C)(C)C1=C(C(=CC(=C1)C(C)(C)C)CN)C(O)C(CO)(CO)CO PLYGVHXICXLDQL-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- QSBINWBNXWAVAK-PSXMRANNSA-N PE-NMe(16:0/16:0) Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OCCNC)OC(=O)CCCCCCCCCCCCCCC QSBINWBNXWAVAK-PSXMRANNSA-N 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- IBVAQQYNSHJXBV-UHFFFAOYSA-N adipic acid dihydrazide Chemical compound NNC(=O)CCCCC(=O)NN IBVAQQYNSHJXBV-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 125000001118 alkylidene group Chemical group 0.000 description 1
- AFVLVVWMAFSXCK-VMPITWQZSA-N alpha-cyano-4-hydroxycinnamic acid Chemical group OC(=O)C(\C#N)=C\C1=CC=C(O)C=C1 AFVLVVWMAFSXCK-VMPITWQZSA-N 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- PYHXGXCGESYPCW-UHFFFAOYSA-N alpha-phenylbenzeneacetic acid Natural products C=1C=CC=CC=1C(C(=O)O)C1=CC=CC=C1 PYHXGXCGESYPCW-UHFFFAOYSA-N 0.000 description 1
- 239000005030 aluminium foil Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000002648 azanetriyl group Chemical group *N(*)* 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- CUBCNYWQJHBXIY-UHFFFAOYSA-N benzoic acid;2-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=CC=C1.OC(=O)C1=CC=CC=C1O CUBCNYWQJHBXIY-UHFFFAOYSA-N 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 230000021523 carboxylation Effects 0.000 description 1
- 238000006473 carboxylation reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000002704 decyl 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])* 0.000 description 1
- LXCYSACZTOKNNS-UHFFFAOYSA-N diethoxy(oxo)phosphanium Chemical compound CCO[P+](=O)OCC LXCYSACZTOKNNS-UHFFFAOYSA-N 0.000 description 1
- 125000001891 dimethoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- YLFBFPXKTIQSSY-UHFFFAOYSA-N dimethoxy(oxo)phosphanium Chemical compound CO[P+](=O)OC YLFBFPXKTIQSSY-UHFFFAOYSA-N 0.000 description 1
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229920005561 epichlorohydrin homopolymer Polymers 0.000 description 1
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 235000019439 ethyl acetate Nutrition 0.000 description 1
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical class CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 1
- OBNCKNCVKJNDBV-UHFFFAOYSA-N ethyl butyrate Chemical compound CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- AHAREKHAZNPPMI-UHFFFAOYSA-N hexa-1,3-diene Chemical compound CCC=CC=C AHAREKHAZNPPMI-UHFFFAOYSA-N 0.000 description 1
- NZYMWGXNIUZYRC-UHFFFAOYSA-N hexadecyl 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NZYMWGXNIUZYRC-UHFFFAOYSA-N 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical group I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 230000033444 hydroxylation Effects 0.000 description 1
- 238000005805 hydroxylation reaction Methods 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 229920002681 hypalon Polymers 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 235000012204 lemonade/lime carbonate Nutrition 0.000 description 1
- 229960004232 linoleic acid Drugs 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229960003511 macrogol Drugs 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 150000002696 manganese Chemical class 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- WGGBUPQMVJZVIO-XFXZXTDPSA-N methyl (z)-2-cyano-3-(4-methoxyphenyl)but-2-enoate Chemical group COC(=O)C(\C#N)=C(\C)C1=CC=C(OC)C=C1 WGGBUPQMVJZVIO-XFXZXTDPSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- YVYHWOZEQUFKOB-UHFFFAOYSA-N n'-[3-(dimethylamino)propyl]oxamide Chemical compound CN(C)CCCNC(=O)C(N)=O YVYHWOZEQUFKOB-UHFFFAOYSA-N 0.000 description 1
- ZZAMUZWGTXZGKY-UHFFFAOYSA-N n-(6-aminohexyl)-3-(3,5-ditert-butyl-4-hydroxyphenyl)propanamide Chemical compound CC(C)(C)C1=CC(CCC(=O)NCCCCCCN)=CC(C(C)(C)C)=C1O ZZAMUZWGTXZGKY-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229920006173 natural rubber latex Polymers 0.000 description 1
- 150000002815 nickel Chemical class 0.000 description 1
- 150000002816 nickel compounds Chemical class 0.000 description 1
- 125000001400 nonyl 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])[H] 0.000 description 1
- 229940038384 octadecane Drugs 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 229960002969 oleic acid Drugs 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 description 1
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- MQOCIYICOGDBSG-UHFFFAOYSA-M potassium;hexadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCC([O-])=O MQOCIYICOGDBSG-UHFFFAOYSA-M 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- KOODSCBKXPPKHE-UHFFFAOYSA-N propanethioic s-acid Chemical compound CCC(S)=O KOODSCBKXPPKHE-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- WBHHMMIMDMUBKC-QJWNTBNXSA-N ricinoleic acid Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(O)=O WBHHMMIMDMUBKC-QJWNTBNXSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- IJRHDFLHUATAOS-DPMBMXLASA-N sodium;(z,12r)-12-hydroxyoctadec-9-enoic acid Chemical compound [Na+].CCCCCC[C@@H](O)C\C=C/CCCCCCCC(O)=O IJRHDFLHUATAOS-DPMBMXLASA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 230000009967 tasteless effect Effects 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- CWERGRDVMFNCDR-UHFFFAOYSA-M thioglycolate(1-) Chemical compound [O-]C(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-M 0.000 description 1
- 239000012745 toughening agent Substances 0.000 description 1
- DPUOLQHDNGRHBS-MDZDMXLPSA-N trans-Brassidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-MDZDMXLPSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 125000002948 undecyl 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])[H] 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1515—Three-membered rings
-
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
- C08K5/375—Thiols containing six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Epoxy Resins (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
含有式(1)的巯甲基苯酚及脂肪酸或脂肪酸酯环
氧化物的稳定剂混合物,尤其适用于稳定含有高弹体
或增粘树脂或即含高弹体又含增粘树脂的组合物。
式I中n及R1到R4的定义见权利要求1。
Description
本发明涉及新的稳定剂混合物,该稳定剂混合物尤其适于含有高弹体或增粘树脂或即含有高弹体又含有增粘树脂的组合物中。
在制备,贮存,加工和最终使用期间,这类组合物常处于改变其性质的多种因素的作用下。温度,大气中的氧,光和剪切力产生的机械应力在此起主要作用。
人们试图通过使用某些稳定剂如抗氧化剂,加工稳定剂,金属减活化剂如光稳定剂来抑制这些影响。例如,从US-A-5,008,459,US-A-4,857,572,US-A-4,820,756,US-A-4,741,864和US-A-4,759,862中可知用双(烷基巯甲基)苯酚来稳定高弹体组合物。按照US-A-3,658,743,稳定剂混合物是由一种苯酚、一种有机硫化合物或硫酯以及一种环氧化物或一种亚磷酸盐所组成,该混合物常用于以硫进行硫化的不饱和高单体。按照GB-A-917,100,热塑性聚烯烃可用由一种环氧化物和如一种苯酚或一种硫代二丙酸酯的抗氧化剂组成的混合物来稳定化。
现已发现一种含有特定的巯甲基苯酚和环氧化物的新的稳定剂混合物,它尤其适于含有高弹体或增粘树脂或即含有高弹性又含有增粘树脂的组合物的稳定化。
因此,本发明提供了一种稳定剂混合物,它包括
(a)式(1)的一种巯甲基苯酚
其中n是0或1,R1和R2彼此独立地为具有1到12个碳原子的烷基或式-CH2SR3的基团,其中R3是具有8到18个碳原子的烷基,苯基或苄基,R4基团彼此独立地为氢或甲基,连接在同一环上的R4基不能同时为甲基,和
(b)一种具有3到22个碳原子的脂肪酸或具有1到18个碳原子的烷基酯的环氧化物,
(a)与(b)的重量比为99∶1到1∶10;尤其是10∶1到1∶10。
本发明还提供了一种含有一种高弹体或一种增粘树脂或即含有一种高弹性又含有一种增粘树脂的组合物,以及如上定义的稳定剂混合物,该混合物适用于稳定含有高弹体或增粘树脂或即含有高弹体又含有增粘树脂的组合物,本发明还提供了使用稳定剂混合物稳定这种组合物的方法。
在组分(a)中,即在式(Ⅰ)化合物中,R1和R2可彼此独立地为具有1到12个碳原子的烷基,例如,甲基,乙基,丙基,丁基,己基,辛基,十一烷基和十二烷基及其相应的支化异构体,也可以是式-CH2SR的基团,其中R3除了是苯基或苄基外也可以是具有6到18个碳原子的烷基,如己基,辛基,壬基,癸基,十二烷基,十四烷基和十八烷基或这类基团的支化异构体。
式(1)的化合物及它们的制备在已被提到的如US-A-4,857,572中已有介绍。
用作组分(b)的脂肪酸和脂肪酸烷基酯的环氧化物包括,例如,环氧化的油酸,亚油酸,亚麻酸,芥酸,蓖麻油酸和巴西烯酸,它们可以是游离的或是与单羟基或多羟基醇酯化的,这些醇如甲醇,丁醇,月桂醇,辛醇以及季戊四醇,丙三醇,乙二醇,丙二醇,丁二醇,新戊二醇,甘露糖醇和山梨糖醇。所述的多羟基醇可被完全酯化或部分酯化。组分(b)还包括环氧化的高级脂肪酸酯的混合物,例如,环氧化的棉子油,蓖麻油或橄榄油,环氧化的动物脂或特别是环氧化的大豆油或亚麻子油。
组分(a)较好地包括式(1)的那些组合物,其中n是0或1,R1和R2是彼此独立地具有1到4个碳原子的烷基或式-CH2SR3的基团,R3是具有6到12个碳原子的烷基及R4基彼此独立地为氢或甲基,连接在同一环上的R4基不同时为甲基。
在式(1)的这些化合物中,其中以n是0,R1是-CH2SC8H17,R2是甲基,R3是辛基和R4基是氢的那些化合物尤其重要。
进一步优选的式(1)化合物是其中n是0,R1是式-CH2SR3的基团,R3是具有6到18个碳原子的烷基、苯基或苄基,R2是氢或具有1到12碳原子的烷基及R4是氢的那些化合物,以及其中n是0,R1是氢或具有1到12个碳原子的烷基,R2是如式-CH2SR3的基团,R3是具有6到18碳原子的烷基,苯基或苄基及R4是氢的那些化合物。
特别优选的式(1)化合物是n为0,R1为式-CH2SR3的基团,R3是具有6到18个碳原子的烷基,苯基或苄基,R2是氢或甲基以及R4是氢的那些化合物。
组分(b)最好是环氧化的脂肪酸酯的混合物,例如,环氧化的蓖麻油或葵花油尤其是环氧化的大豆油或亚麻子油。
按照本发明的组合物中稳定剂混合物的优选量相对于高弹体或增粘树脂或高弹体与增粘树脂为0.01-10%(重量)。
按照本发明的化合物可包括的高弹体是,例如:
1.聚二烯,例如,聚丁二烯,聚异戊二烯,聚氯丁二烯,嵌段共聚物,例如,苯乙烯/丁二烯/苯乙烯或苯乙烯/异戊二烯/苯乙烯;以及如丙烯腈/丁二烯和苯乙烯/丁二烯这样的共聚物。
2.单烯和二烯互相之间的共聚物或与其它乙烯基单体的共聚物,例如乙烯-烷基丙烯酸酯共聚物,乙烯-烷基甲基丙烯酸酯共聚物,乙烯-醋酸乙烯酯共聚物以及乙烯与丙烯和一种二烯的三元共聚物;如己二烯,二环戊二烯或亚乙基降冰片烯。
3.含卤素聚合物,例如,氯丁橡胶,氯化橡胶,氯化或氯磺化聚乙烯,3-氯-1,2-环氧丙烷均聚物和共聚物,一氯三氟化乙烯共聚物,含卤素的乙烯基化合物的聚合物,例如,聚亚乙烯基氯化物和聚亚乙烯基氟化物;以及它们的共聚物,如乙烯基氯化物-亚乙烯基氯化物,乙烯基氯化物-蜡酸乙烯酯或亚乙烯基氯化物-蜡酸乙烯酯。
4.从聚醚,聚酯和聚丁二烯衍生物得到的聚氨基甲酸酯,象它们的前体一样一端具有端羟基,另一端具有脂肪的或芳香的聚异氰酸酯。
5.天然橡胶。
6.上面所得到的聚合物混合物(掺聚料)。
7.天然或合成橡胶的水分散体,例如,天然橡胶胶乳或羧化的苯乙烯-丁二烯共聚物胶乳。
如果需要,这些处于胶乳形态的高弹体也可被稳定化。
聚二烯如聚丁二烯橡胶,它的共聚物,如苯乙烯/丁二烯橡胶或直链或支化的苯乙烯/丁二烯/苯乙烯、苯乙烯/异戊二烯/苯乙烯嵌段共聚物,乙烯/醋酸乙烯酯共聚物或聚氨基甲酸酯可以较好地加以使用。
按照本发明的组合物可包括的增粘树脂是,例如:
天然松香树脂如脂松香,木蒸松香或浮油松香。
松香树脂的衍生物,如丙三醇酯和季戊四醇酯,在每种情况下是氢化或非氢化,歧此或非歧化的。
合成的烃类树脂,特别是具有5或9个碳原子。
聚茚树脂,甲基茚树脂和苯并呋喃-茚树脂。
萜烯树脂。
甲基苯乙烯树脂。
酚醛树脂。
其它增粘剂如石油沥清或沥青。
上面所述树脂的混合物。
上面所述树脂的水乳液。
一种合成烃类树脂,特别是具有5或9个碳原子的烃类树脂,松香树脂或松香树脂的衍生物是可以优先采用的。
按照本发明的稳定剂混合物在高弹体中或在增粘树脂中或在高弹体和增粘树脂中的混合可如下进行。例如在沉淀之前向聚合物溶液或胶乳中添加相应的稳定剂溶液或乳液/分散液,或在成型过程之中或之前按本领域中惯用的方法将它们混合,如果适当地随后进行溶剂的蒸发也可向聚合物中加入溶解的或分散的化合物。稳定剂混合物也可以含有该混合物的母炼胶的形式被加入到聚合物中,例如重量浓度为2.5-25%。
因为增粘树脂是粘合剂的起始物料,所以在稳定化的粘合剂的制备过程中本发明提供的稳定剂混合物能成功地用作增粘树脂的稳定剂这一事实是极重要的。因此可能在原在原料步骤就已将它们稳定,从加工工艺观点来看这是很重要的。
粘合剂通常是含有高弹体,增粘树脂及其它成分蜡或油的组合物。适于粘合剂的蜡是,例如,石蜡或微蜡或费-托合成过程中得到的蜡;它们可以是天然的或是合成的。油的实例是芳香油,脂环烃或石蜡油,它们的选择尤其是基于使用时的溶解性和分子量。
与本发明有关,能用作热熔胶的组合物是特别感兴趣的,这些包括,作为高弹体和增粘树脂上面所列的物质是优选的,尤其是直链或支化的苯乙烯/丁二烯/苯乙烯或苯乙烯/异戊二烯/苯乙烯嵌段共聚物以及松香树脂或合成的烃类树脂。通过使用本发明提供的稳定剂混合物可以有效地保护这种类型的热熔胶免受开始所提到的不利影响,因此粘合剂可以在更长的时间里保持它们起始的粘合性和透明性或浅的本色。
可以用在本发明组合物中的其它添加剂是,例如:
1.抗氧化剂
1.1和1.2.烷基化的单酚,例如2,6-二叔丁基-4-甲基苯酚,2-叔丁基-4,6-二甲基苯酚,2,6-二叔丁基-4-乙基苯酚,2,6-二叔丁基-4-正丁基苯酚,2,6-二叔丁基-4-异丁基苯酚,2,6-二-环戊基-4-甲基苯酚,2-(α-甲基环己基)-4,6-二甲基苯酚,2,6-二-十八烷基-4-甲基苯酚,2,4,6-三环己基苯酚,2,6-二叔丁基-4-甲氧基甲基苯酚,2,6-二壬基-4-甲基苯酚,2,4-二甲基-6-(1′-甲基-十一烷-1′-基)苯酚,2,4-二甲基-6-(1′-甲基-十七烷-1′-基)苯酚,2,4-二甲基-6-(1′-甲基-十三烷-1′-基)苯酚和它们的混合物。
1.2.烷基硫代甲基苯酚,例如2,4-二辛基硫代甲基-6-叔丁基苯酚,2,4-二辛基硫代甲基-6-甲基苯酚,2,4-二辛基硫代甲基-6-乙基苯酚,2,6-二-十二烷基硫代甲基-4-壬基苯酚。
1.3.氢醌和烷基化的氢醌,例如2,6-二叔丁基-4-甲氧基苯酚,2,5-二叔丁基-氢醌,2,5-二叔戊基-氢醌,2,6-二苯基-4-十八烷氧基苯酚,2,6-二叔丁基-氢醌,2,5-二叔丁基-4-羟基苯甲醚,3,5-二叔丁基-4-羟基苯甲醚,3,5-二叔丁基-4-羟苯基硬脂酸酯,和二(3,5-二叔丁基-4-羟苯基)己二酸酯。
1.4.羟基化硫代二苯基醚,例如2,2′-硫代-二(6-叔丁基-4-甲基苯酚),2,2′-硫代-二(4-辛基苯酚),4,4′-硫代-二(6-叔丁基-3-甲基苯酚),4,4′-硫代-二(6-叔丁基-2-甲基苯酚),4,4′-硫代-二(3,6-仲戊基苯酚),和4,4′-二(2,6-二甲基-4-羟苯基)二硫化物。
1.5.亚烷基化-二苯酚,例如2,2′-亚甲基-二(6-叔丁基-4-甲基苯酚),2,2′-亚甲基-二(6-叔丁基-4-乙基苯酚),2,2′-亚甲基-二[4-甲基-6-(α-甲基环己基)苯酚),2,2′-亚甲基-二(4-甲基-6-环己基苯酚),2,2′-亚甲基-二(6-壬基-4-甲基苯酚),2,2′-亚甲基-二[4,6-二叔丁基苯酚],2,2′-亚甲基-二(4,6-二叔丁基苯酚),2,2′-亚乙基-二(6-叔丁基-4-异丁基苯酚),2,2′-亚甲基-二[6-(α-甲基苄基)-4-壬基苯酚],2,2′-亚甲基-二[6-(α,α-二甲基苄基)-4-壬基苯酚],4,4′-亚甲基-二(2,6-二叔丁基苯酚),4,4′-亚甲基-二(6-叔丁基-2-甲基苯酚),1,1-二(5-叔丁基-4-羟基-2-甲基苯基)-丁烷,2,6-二(3-叔丁基-5-甲基-2-羟苄基)-4-甲基苯酚,1,1,3-三(5-叔丁基-4-羟基-2-甲基苯基)丁烷,1,1-二(5-叔丁基-4-羟基-2-甲基苯基)-3-正十二烷基巯基丁烷,乙二醇-二[3,3-二(3′-叔丁基-4-′羟苯基)丁酸酯],二(3-叔丁基-4-羟基-5-甲基苯基)二环戊二烯,二[2-(3′-叔丁基-2′-羟基-5′-甲基苄基)-6-叔丁基-4-甲基苯基]对苯二甲酸酯,1,1-二(3,5-二甲基-2-羟苯基)丁烷,2,2-二(3,5-二叔丁基-4-羟苯基)丙烷,2,2-二(5-叔丁基-4-羟基-2-甲基苯基)-4-正十二烷基巯基丁烷和1,1,5,5-四(5-叔丁基-4-羟基-2-甲基苯基)戊烷。
1.6.O-,N-和S-苄基化合物,例如3,5,3′,5′-四叔丁基-4,4′-二羟基二苄基醚,十八烷基-4-羟基-3,5-二甲基苄基巯基乙酸酯,三(3,5-二叔丁基-4-羟苄基)胺,二(4-叔丁基-3-羟基-2,6-二甲基苄基)二硫代对苯二甲酸酯,二(3,5-二叔丁基-4-羟苄基)硫化物,和异辛基-3,5-二叔丁基-4-羟苄基巯基乙酸酯。
1.7.羟苄化的丙二酸酯,例如二-十八烷基-2,2-二(3,5-二叔丁基-2-羟苄基)丙二酸酯,二-十八烷基-2-(3-叔丁基-4-羟基-5-甲基苄基)丙二酸酯,二-十二烷基巯乙基-2,2-二(3,5-二叔丁基-4-羟苄基)丙二酸酯,二-[4-(1,1,3,3-四甲基丁基)苯基]-2,2-二(3,5-二叔丁基-4-羟苄基)丙二酸酯。
1.8.羟苄基-芳香化合物,例如1,3,5-三(3,5-二叔丁基-4-羟苄基)-2,4,6-三甲基苯,1,4-二(3,5-二叔丁基-4-羟苄基)2,3,5,6-四甲基苯,2,4,6-三(3,5-二叔丁基-4-羟苄基)苯酚。
1.9.三嗪化合物,例如,2,4-二辛基巯基-6-(3,5-二叔丁基-4-羟基苯胺基)-1,3,5-三嗪,2,-辛基巯基-4,6-二(3,5-二叔丁基-4-羟基苯胺基)-1,3,5-三嗪,2-辛基巯基-4,6-二(3,5-二叔丁基-4-羟基苯氧基)-1,3,5-三嗪,2,4,6-三(3,5-二叔丁基-4-羟基苯氧基)-1,2,3-三嗪,1,3,5-三(3,5-二叔丁基-4-羟苄基)异氰酸酯,1,3,5-三(4-叔丁基-3-羟基-2,6-二甲基苄基)异氰酸酯,2,4,6-三(3,5-二叔丁基-4-羟苯基乙基)-1,3,5-三嗪,1,3,5-三(3,5-二叔丁基-4-羟苯基丙酰基)六氢化1,3,5-三嗪和1,3,5-三(3,5-二环己基-4-羟苄基)异氰酸酯。
1.10.苄基膦酸酯,例如,2,5-二叔丁基-4-羟苄基膦酸二甲酯,3,5-二叔丁基-4-羟苄基膦酸二乙酯,5-叔丁基-4-羟基-3-甲基苄基膦酸二-十八烷基酯和单乙基3,5-二叔丁基-4-羟基苄基膦酸二-十八烷基酯的钙盐。
1.11.酰氨基酚,例如,4-羟基月桂酸N-酰苯胺,4-羟基硬脂酸N-酰苯胺和N-(3,5-二叔丁基-4-羟苯基)氨基甲酸辛基酯。
1.12.β-(3,5-二叔丁基-4-羟苯基)丙酸与单羟基或多羟基醇形成的酯,例如与甲醇、乙醇、十八醇,1,6-己二醇,1,9-壬二醇,乙二醇,1,2-丙二醇,新戊二醇,硫代二甘醇,二甘醇,三甘醇,季戊四醇,三(羟乙基)异氰酸酯,N,N′-二(羟乙基)草酸肼,3-硫代十一烷醇,3-硫代十五烷醇,三甲基己二醇,三羟甲基丙烷和4-羟甲基-1-磷杂-2,6,7-三氧杂双环[2,2,2]辛烷形成的酯。
1.13.β-(5-叔丁基-4-羟基-3-甲基苯基)丙酸与单羟基或多羟基醇形成的酯,例如与甲醇,乙醇,十八烷醇,1,6-己二醇,1,9-壬二醇,乙二醇,1,2-丙二醇,新戊二醇,硫代二甘醇,二甘醇,三甘醇,季戊四醇,三(羟基)乙基异氰酸酯,N,N′-二(羟乙基)草酸肼,3-硫代十一烷醇,3-硫代十五烷醇,三甲基己二醇,三羟甲基丙烷和4-羟基甲基-1-磷杂-2,6,7-三氧杂双环[2,2,2]辛烷形成的酯。
1.14.β-(3,5-二环己基-4-羟苯基)丙酸与单羟基或多羟基醇形成的酯,例如,与甲醇,乙醇,十八烷醇,1,6-己二醇,1,9-壬二醇,乙二醇,1,2-丙二醇,新戊二醇,硫代二甘醇,二甘醇,三甘醇,季戊四醇,三(羟基)乙基异氰酸酯,N,N′-二(羟乙基)草酸肼,3-硫代十一烷醇,3-硫代十五烷醇,三甲基己二醇,三羟甲基丙烷和4-羟甲基-1-磷杂-2,6,7-三氧杂双环[2,2,2]辛烷形成的酯。
1.15.3,5-二叔丁基-4-羟苯基乙酸与单羟基或多羟基醇形成的酯,例如,与甲醇,乙醇,十八烷醇,1,6-己二醇,1,9-壬二醇,乙二醇,1,2-丙二醇,新戊二醇,硫代二甘醇,二甘醇,三甘醇,季戊四醇,三(羟基)乙基异氰酸酯,N,N′-二(羟乙基)草酸肼,3-硫代十一烷醇,3-硫代十五烷醇,三甲基己二醇,三羟甲基丙烷和4-羟基甲基-1-磷杂-2,6,7-三氧杂双环[2,2,2]辛烷形成的酯。
1.16.β-(3,5-二叔丁基-4-羟苯基)丙酸的酰胺,例如N,N′-二(3,5-二叔丁基-4-羟苯基丙酰基)六亚甲基二胺,N,N′-二(3,5-二叔丁基-4-羟苯基丙酰基)三亚甲基二胺和N,N′-二(3,5-二叔丁基-4-羟苯基丙酰基)肼。
2.UV-吸收剂和光稳定剂
2.1.2-(2′-羟苯基)苯并三唑化合物,例如5′-甲基-,3′,5′-二叔丁基-,5′-叔丁基-,5′-(1,1,3,3-四甲基丁基)-,5-氯-3′,5′-二叔丁基-,5-氯-3′-叔丁基-5′-甲基-,3′-仲丁基-5′-叔丁基-,4′-辛氧基-,3′,5′-二叔戊基-,3′,5′-二(α,α-二甲基苄基)-,5-氯-3′-叔丁基-5′-(2-辛氧基羰基乙基)-和5-氯-3′-叔丁基-5′-[2-(2-乙基己氧基)羰基乙基]-的混合物,5-氯-3′-叔丁基-5′-(2-辛氧基羰基乙基)-,3′-叔丁基-5′-(2-甲氧基羰基乙基)-,3′-叔丁基-5′-(2-辛氧基羰基乙基)-,3′-叔丁基-5′-[2-(2-乙基己氧基)羰基乙基]-,3′-十二烷基-5′-甲基-和3′-叔丁基-5′-(2-异辛氧基羰基乙基)-2′-羟苯基-2H-苯并三唑(2),2,2′-亚甲基-二[4-(1,1,3,3-四甲基丁基)-6-苯并三唑-2-基苯酚];2-[3′-叔丁基-5′-(2-甲氧基羰基乙基)-2-羟苯基]-2H-苯并三唑与聚乙二醇300的酯基转移产物;[R-CH2CH2-COO(CH2)3 ,其中R=3′-叔丁基-4′-羟基-5′-2H-苯并三唑-2-基苯基。
2.2.2-羟基二苯甲酮,例如4-羟基,4-甲氧基,4-辛氧基,4-癸氧基,4-十二烷氧基,4-苄氧基,4,2′,4′-三羟基和2′-羟基-4,4′-二甲氧基的衍生物。
2.3取代的或未取代的苯甲酸酯,例如水杨酸4-叔丁基-苯基酯,水杨酸苯酯,水杨酸辛基苯基酯,二苯甲酰间苯二酚,二(4-叔丁基-苯甲酰基)间苯二酚,苯甲酰基间苯二酚,3,5-二叔丁基-4-羟基苯甲酸2,4-二叔丁基苯酯,3,5-二叔丁基-4-羟基苯甲酸十六烷基酯,3,5-二叔丁基-4-羟基苯甲酸十八烷基酯和3,5-二叔丁基-4-羟基苯甲酸2-甲基-4,6-二叔丁基苯基酯。
2.4.丙烯酸酯,例如α-氰基β,β-二苯基丙烯酸乙基和异辛基酯,α-甲酯基肉桂酸甲基酯,α-氰基-β-甲基-对甲氧基肉桂酸甲基和丁基酯,α-甲酯基-对-甲氧基肉桂酸甲基酯和N-(β-甲酯基-β-氰基乙烯基)-2-甲基二氢吲哚。
2.5.镍化合物,例如2,2′-硫代-二[1,1,3,3-四甲基苯基)苯酚]的镍配合物,如以1∶1或1∶2配合,如果需要可用其它配位体,如正丁基胺,三乙醇胺或N-环己基二乙醇胺,二丁基硫代氨基甲酸镍,4-羟基-3,5-二叔丁基苄基膦酸单烷酯,如甲基或乙基酯的镍盐,酮肟的镍配合物,如2-羟基-4-甲基苯基十一烷基酮肟的镍配合物,以及1-苯基-4-月桂酰基-5-羟基吡唑的镍配合物,需要时可用其它配位体。
2.6.具有空间位阻的胺,例如二(2,2,6,6-四甲基哌啶基)癸二酸酯,二(2,2,6,6-四甲基哌啶基)琥珀酸酯,二(1,2,2,6,6-五甲基哌啶基)癸二酸酯,二(1,2,2,6,6-五甲基哌啶基)正丁基-3,5-二叔丁基-4-羟苄基丙二酸酯,1-羟基乙基-2,2,6,6-四甲基-4-羟基哌啶和琥珀酸的缩合产物,N,N′-二(2,2,6,6-四甲基-4-哌啶基)-六亚甲基二胺和4-叔辛烷基氨基-2,6-二氯-1,3,5-S-三嗪的缩合产物,三(2,2,6,6-四甲基-4-哌啶基)次氮基乙酸酯,四(2,2,6,6-四甲基-4-哌啶基)1,2,3,4-丁烷四酸酯(butanetetraoate),1,1′-(1,2-乙二基)二(3,3,5,5-四甲基哌嗪酮),4-苯甲酰基-2,2,6,6-四甲基哌啶,4-硬脂酰氧基-2,2,6,6-四甲基哌啶,二(1,2,2,6,6-五甲基哌啶基)2-正丁基-2-(2-羟基-3,5-二叔丁基苄基)丙二酸酯,3-正辛基-7,7,9,9-四甲基-1,3,8-三氮杂螺[4,5]正癸烷-2,4-二酮,二(1-辛氧基-2,2,6,6-四甲基哌啶基)癸二酸酯,二(1-辛氧基-2,2,6,6-四甲基哌啶基)琥珀酸酯,N,N′-二(2,2,6,6-四甲基-4-哌啶基)六亚甲基二胺与4-吗啉代-2,6-二氯-1,3,5-三嗪的缩合产物,2-氯-4,6-二(4-正丁氨基-2,2,6,6-四甲基哌啶基)-1,3,5-三嗪与1,2-三(3-氨基丙基氨基)乙烷的缩合产物,2-氯-4,6-二(4-正丁基氨基-1,2,2,6,6-五甲基哌啶基)-1,3,5-三嗪和1,2-二(3-氨基丙基氨基)乙烷的缩合产物,8-乙酰基-3-十二烷基-7,7,9,9-四甲基-1,3,8-三氮杂螺[4,5]正癸烷-2,4-二酮,3-十二烷基-1-(2,2,6,6-四甲基-4-哌啶基)吡咯烷-2,5-二酮。
2.7.草酸肼,例如4,4′-二辛基氧基N,N′-草酰二苯胺,2,2′-二辛基氧基-5,5′-二叔丁基N,N′-草酰二苯胺,2,2′-二-十二烷氧基-5,5′-二叔丁基N,N′-草酰二苯胺,2-乙氧基-2′-乙基-N,N′-草酰二苯胺,N,N′-二(3-二甲基氨基丙基)草酰胺,2-乙氧基-5-叔丁基-2′-乙基N,N′-草酰二苯胺及其与2-乙氧基-2′-乙基-5,4′-二叔丁基N,N′-草酰二苯胺的混合物,以及邻和对位甲氧基二取代的N,N′-草酰二苯胺的混合物和邻-和对-乙氧基二取代的N,N′-草酰二苯胺的混合物。
2.8.2-(2-羟苯基)1,3,5-三嗪,例如2,4,6-三(2-羟基-4-辛氧基苯基)-1,3,5-三嗪,2-(2-羟基-4-辛氧基苯基)-4,6-二(2,4-二甲基苯基)-1,3,5-三嗪,2-(2,4-二羟苯基)-4,6-二(2,4-二甲基苯基)-1,3,5-三嗪,2,4-二(2-羟基-4-丙氧基苯基)-6-(2,4-二甲基苯基)-1,3,5-三嗪,2-(2-羟基-4-十二烷氧基苯基)-4,6-二(2,4-二甲基苯基)-1,3,5-三嗪,2-[2-羟基-4-(2-羟基-3-丁氧基丙氧基)苯基]-4,6-二(2,4-二甲基苯基)-1,3,5-三嗪,2-[2-羟基-4-(2-羟基-3-辛基-3-辛氧基丙氧基)苯基]-4,6-二(2,4-二甲基苯基)-1,3,5-三嗪。
3.金属减活化剂,例如N,N′-二苯基草酸肼,N-水杨醛-N′-水杨酰肼,N,N′-二(水杨酰基)肼,N,N′-二(3,5-二叔丁基-4-羟苯基丙酰基)肼,3-水杨酰氨基-1,2,4-三唑,二(亚苄基)草酸二酰肼,N,N′-草酰二苯胺,间苯二甲酸二酰肼,脂肪酸二苯基酰肼,N,N′-二乙缩醛己二酸二酰肼,N,N′-二水杨酰基草酸二酰肼,及N,N′-二-水杨酰基硫代丙酸二酰肼。
4.亚磷酸酯和亚膦酸酯(phosphonites),例如三苯基亚磷酸酯,二苯基烷基亚磷酸酯,苯基二烷基亚磷酸酯,三(壬基苯基)亚磷酸酯,三月桂基亚磷酸酯,三-十八烷基亚磷酸酯,二硬脂酰季戊四醇二亚磷酸酯,三(2,4-二叔丁基苯基)亚磷酸酯,二异癸基季戊四醇二亚磷酸酯,二(2,4-二叔丁基苯基)季戊四醇二亚磷酸酯,(2,6-二叔丁基-4-甲基苯基)季戊四醇二亚膦酸酯,二异癸基氧基季戊四醇二亚磷酸酯,二(2,4-二叔丁基-6-甲基苯基)季戊四醇二亚磷酸酯,二(2,4,6-三叔丁基苯基)季戊四醇二亚磷酸酯,三硬脂酰山梨糖醇三亚磷酸酯,四(2,4-二叔丁基苯基)-4,4′-二亚苯基二亚膦酸酯,6-异辛氧基-2,4,8,10-四叔丁基-12H-二苯并[d,g]-1,3,2-dioxaphosphocine和6-氟-2,4,8,10-四叔丁基-12-甲基二苯并[d,g]-1,3,2-dioxaphosphocine。
5.过氧化物消除剂,例如β-硫代二丙酸酯,如月桂基,十八烷基,十四烷基或十三烷基酯,巯基苯并咪唑,2-巯基苯并咪唑锌盐,二丁基二硫代氨基甲酸锌,二-十八烷基二硫化物,以及季戊四醇四(β-十二烷基巯基)丙酸酯。
6.聚酰胺稳定剂,例如与碘化物和/或磷化合物结合的铜盐以及二价的锰盐。
7.碱性协同稳定剂,例如蜜胺,聚乙烯吡咯烷酮,双氰胺,三烯丙基氰尿酸酯,脲衍生物,肼衍生物,胺,聚酰胺,聚尿烷,高级脂肪酸的碱金属盐和碱土金属盐,例如硬脂酸钙,硬脂酸锌,山萮酸镁,硬脂酸镁,蓖麻醇酸钠,棕榈酸钾,焦儿茶酸锑或焦儿茶酸锡。
8.成核剂,例如4-叔丁基苯甲酸,己二酸和二苯基乙酸。
9.填充剂和增强剂,例如碳酸钙,硅酸盐,玻璃纤维,滑石粉,高岭土,云母,硫酸钡,金属氧化物和金属氢氧化物,碳黑和石墨。
10.其它添加剂,例如,增塑剂,润滑剂,乳化剂,颜料,荧光增白剂,阻燃剂,抗静电剂和促进剂。
11.交联剂,如有机过氧化物,硫,氧化锌,硬脂酸和硫化促进剂。
下列实施例详细地说明了本发明,分数和百分率按重量计。
实施例1:稳定剂混合物的制备:
以任意可能的组分(a)和(b)重量比通过简单地混合即可制得稳定剂混合物。详细地说,方法是混合物被加热到大约120℃,同时进行搅拌,在此温度保持2小时,然后冷却,这样制得的稳定剂混合物是无味的。
实施例2:热熔胶的制备及熟化
a)100份的ESCOREZ
5380(作为增粘树脂的一种合成的氢化的烃类树脂),50份的SHELLFLEX
451(作为增塑剂的一种环烷基矿物油)以及在适当时,于175℃混入如下所示量的稳定剂混合物,在实验室混合器中经搅拌得到均匀的熔化物,向该熔化物中逐份加入50份的CARIFLEX
107(用作高弹体的一种直链苯乙烯/异戊二烯/苯乙烯嵌段共聚物)。在2小时后混合操作完成。包括20份的样品放入玻璃盘中并用铝箔覆盖,在170℃的循环空气炉中熟化样品3天,结果如表1。
A是式(1)的化合物,其中n是,R1是-CH2SC8H17,R2是甲基,R3是辛基及R4是氢,B是环氧化的大豆油(ReoplastR392)。
b)重复a)中所述的步骤,但高弹体是用50份的FINAPRENERF424(一种支化的苯乙烯/异戊二烯/苯乙烯嵌段共聚物)。结果如表2。
从表中可以看出组分A和组分B的混合物的稳定化能力超过组分A和组分B各自的稳定化能力。
Claims (12)
2、根据权利要求1的稳定剂混合物,其中(a)和(b)的重量比为10∶1到1∶10。
3、根据权利要求1或权利要求2任一项的稳定剂混合物,其中n是0或1,R1和R2彼此独立地是具有1到4个碳原子的烷基或式-CH2SR3的基团,R3是具有6-12个碳原子的烷基,R4基彼此独立地是氢或甲基,连接在同一环上的R4基不同时是甲基。
4、根据权利要求1或权利要求2中任一个的稳定剂混合物,其中n是0或1,R1是-CH2SC8H17,R2是甲基,R3是辛基以及R4是氢。
5、根据权利要求1或权利要求2任一项的稳定剂混合物,其中n是0,R1是式-CH2SR3的基团,其中R3是具有6-18个碳原子的烷基,苯基或苄基,R2是氢或具有1-12个碳原子的烷基及R4是氢。
6、根据权利要求1或权利要求2任一项的稳定剂混合物,其中n是0,R1是氢或具有1-12个碳原子的烷基,R2是式-CH2SR3的基团,其中R3是具有6-18个碳原子的烷基,苯基或苄基及R4是氢。
7、根据权利要求1或权利要求2任一项的稳定剂混合物,其中n是0,R1是氢或具有1-12个碳原子的烷基,R2是-CH2SR3基团,其中R3是具有6-18个碳原子的烷基,苯基或苄基,R2是氢或甲基及R4是氢。
8、根据权利要求1或权利要求2任一项的稳定剂混合物,其中(b)是脂肪酸酯环氧化物的混合物,特别是环氧化的大豆油或亚麻子油。
9、一种包括一种高弹体或一种增粘树脂或者是高弹体和增粘树脂以及权利要求1的稳定剂混合物的组合物。
10、根据权利要求8的组合物,该组合物含有,作为高弹体的直链或支化的苯乙烯/丁二烯/苯乙烯或苯乙烯/异戊二烯/苯乙烯嵌段共聚物和作为增粘树脂的松香树脂或合成的烃类树脂。
11、利用根据权利要求1到8任一项的稳定剂混合物稳定含有高弹体或增粘树脂或即含有高弹体又含有增粘树脂的组合物。
12、一种通过使用权利要求1到8任一项的稳定剂混合物稳定含有高弹体或增粘树脂或即含高弹体又含增粘树脂的组合物的方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH359291 | 1991-12-06 | ||
CH3592/91-3 | 1991-12-06 | ||
CH3592/913 | 1991-12-06 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1073460A true CN1073460A (zh) | 1993-06-23 |
CN1040007C CN1040007C (zh) | 1998-09-30 |
Family
ID=4259315
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN92114141A Expired - Lifetime CN1040007C (zh) | 1991-12-06 | 1992-12-05 | 稳定剂混合物 |
Country Status (16)
Country | Link |
---|---|
US (1) | US5276258A (zh) |
EP (1) | EP0545865B1 (zh) |
JP (1) | JP3113958B2 (zh) |
KR (1) | KR100259023B1 (zh) |
CN (1) | CN1040007C (zh) |
AU (1) | AU660203B2 (zh) |
BR (1) | BR9204852A (zh) |
CA (1) | CA2084588C (zh) |
CZ (1) | CZ357292A3 (zh) |
DE (1) | DE59205477D1 (zh) |
ES (1) | ES2084328T3 (zh) |
HK (1) | HK1004754A1 (zh) |
MX (1) | MX9206996A (zh) |
RU (1) | RU2109027C1 (zh) |
TW (1) | TW222293B (zh) |
ZA (1) | ZA929420B (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1117771C (zh) * | 1997-04-29 | 2003-08-13 | 美国3M公司 | 键合的紫外光吸收剂 |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE190295T1 (de) * | 1991-07-23 | 2000-03-15 | Tri Tex Australia Pty Ltd | Nicht-bituminöses schalldämpfendes material |
AU682287B2 (en) | 1995-05-10 | 1997-09-25 | Morton International, Inc. | Latent mercaptans as multi-functional additives for halogen-containing polymer compositions |
US5852086A (en) * | 1996-09-30 | 1998-12-22 | The Goodyear Tire & Rubber Company | Polyamide-acrylonitrile butadiene blends with reduced gel and antigel agent |
CA2194210A1 (en) * | 1996-12-31 | 1998-06-30 | Bayer Inc. | Process for making stabilised non-coloured rubber |
DE19700967C2 (de) * | 1997-01-14 | 2000-04-27 | Continental Ag | Verwendung einer Kautschukmischung zur Herstellung von Fahrzeugreifen |
TW491833B (en) | 2000-01-10 | 2002-06-21 | Ciba Sc Holding Ag | Improved process for the preparation of mercaptomethylphenols |
US20060014862A1 (en) * | 2004-07-15 | 2006-01-19 | Dzikowicz Robert T | Vulcanizing latex compounds without the use of metal oxide activators or a zinc based accelerator |
KR20090006194A (ko) * | 2006-04-13 | 2009-01-14 | 사이텍 테크놀러지 코포레이션 | 안정화된 스판덱스 조성물 |
US8101679B2 (en) * | 2007-03-21 | 2012-01-24 | Basf Se | Processing stabilizers for rubber compounding |
RU2464291C1 (ru) * | 2011-02-28 | 2012-10-20 | Общество с ограниченной ответственностью "Эластохим" | Смола для повышения клейкости резиновых смесей |
WO2017223173A1 (en) | 2016-06-21 | 2017-12-28 | Bridgestone Americas Tire Operations, Llc | Methods for treating inner liner surface, inner liners resulting therefrom and tires containing such inner liners |
US11697260B2 (en) | 2016-06-30 | 2023-07-11 | Bridgestone Americas Tire Operations, Llc | Methods for treating inner liners, inner liners resulting therefrom and tires containing such inner liners |
WO2018112125A1 (en) | 2016-12-15 | 2018-06-21 | Bridgestone Americas Tire Operations, Llc | Sealant-containing tire and related processes |
JP6848062B2 (ja) | 2016-12-15 | 2021-03-24 | ブリヂストン アメリカズ タイヤ オペレーションズ、 エルエルシー | 硬化したインナーライナー上にポリマー含有コーティングを生成する方法、かかるインナーライナーを含むタイヤを製造する方法、及びかかるインナーライナーを含むタイヤ |
US12103338B2 (en) | 2016-12-15 | 2024-10-01 | Bridgestone Americas Tire Operations, Llc | Sealant layer with barrier, tire containing same, and related processes |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH257412A (de) * | 1944-12-30 | 1948-10-15 | Firestone Tire & Rubber Co | Verfahren zur Herstellung von gummiähnlichen Materialien mit erhöhtem Haftvermögen und nach diesem Verfahren erhaltenes Material. |
DE1218724B (de) * | 1960-03-28 | 1966-06-08 | Du Pont | Verfahren zum Stabilisieren von Homo- oder Mischpolymerisaten von Propylen |
NL129756C (zh) * | 1965-04-21 | 1900-01-01 | ||
US3903173A (en) * | 1967-03-17 | 1975-09-02 | Ciba Geigy Ag | Lower alkylthiomethylene containing phenols |
US3658743A (en) * | 1970-04-30 | 1972-04-25 | Uniroyal Inc | Stabilization of unsaturated hydrocarbon elastomers by synergistic combination of a phenolic compound an organic sulfide or thioester and an epoxide or phosphite ester |
DE3342307A1 (de) * | 1983-11-23 | 1985-05-30 | Bayer Ag, 5090 Leverkusen | Haftschmelzklebstoffe, ihre herstellung und verwendung |
EP0165209B1 (de) * | 1984-06-12 | 1989-07-19 | Ciba-Geigy Ag | o,p-Bifunktionalisierte, o'-substituierte Phenole |
US4741864A (en) * | 1985-10-07 | 1988-05-03 | General Electric Company | Ultraviolet light stable flame retarded polycarbonate blends |
EP0224442B1 (de) * | 1985-11-13 | 1990-05-16 | Ciba-Geigy Ag | Substituierte Phenole als Stabilisatoren |
EP0252006B1 (de) * | 1986-06-26 | 1990-02-28 | Ciba-Geigy Ag | Neue substituierte Phenole und deren Verwendung als Stabilisatoren |
US4835200A (en) * | 1986-12-19 | 1989-05-30 | Shell Oil Company | Color stable hot melt adhesive |
EP0273013B2 (de) * | 1986-12-24 | 1996-07-24 | Ciba-Geigy Ag | Substituierte Phenole als Stabilisatoren |
CA1324857C (en) * | 1987-01-12 | 1993-11-30 | Gary M. Carlson | Stabilized moisture curable polyurethane coatings |
US4707300A (en) * | 1987-03-09 | 1987-11-17 | The Goodyear Tire & Rubber Company | Autosynergistic phenolic antioxidant reaction product |
DE59003449D1 (de) * | 1989-08-30 | 1993-12-16 | Ciba Geigy | Phenolische Verbindungen als Kettenabbrecher für die anionische Lösungspolymerisation von Dienen. |
KR0168058B1 (ko) * | 1990-05-22 | 1999-03-20 | 윌터 클리웨인,한스-피터 위트린 | 탄성중합체용 안정화제 혼합물 |
US5128397A (en) * | 1991-05-09 | 1992-07-07 | Ciba-Geigy Corporation | Stabilized ethylene-vinyl acetate copolymer hot melt adhesive systems |
-
1992
- 1992-11-25 TW TW081109449A patent/TW222293B/zh not_active IP Right Cessation
- 1992-11-27 ES ES92810922T patent/ES2084328T3/es not_active Expired - Lifetime
- 1992-11-27 EP EP92810922A patent/EP0545865B1/de not_active Expired - Lifetime
- 1992-11-27 DE DE59205477T patent/DE59205477D1/de not_active Expired - Lifetime
- 1992-12-02 US US07/984,600 patent/US5276258A/en not_active Expired - Lifetime
- 1992-12-03 AU AU29882/92A patent/AU660203B2/en not_active Expired
- 1992-12-03 RU RU92004595A patent/RU2109027C1/ru active
- 1992-12-04 ZA ZA929420A patent/ZA929420B/xx unknown
- 1992-12-04 MX MX9206996A patent/MX9206996A/es unknown
- 1992-12-04 CZ CS923572A patent/CZ357292A3/cs unknown
- 1992-12-04 CA CA002084588A patent/CA2084588C/en not_active Expired - Lifetime
- 1992-12-04 BR BR9204852A patent/BR9204852A/pt not_active IP Right Cessation
- 1992-12-05 CN CN92114141A patent/CN1040007C/zh not_active Expired - Lifetime
- 1992-12-05 KR KR1019920023445A patent/KR100259023B1/ko not_active IP Right Cessation
- 1992-12-07 JP JP04351256A patent/JP3113958B2/ja not_active Expired - Lifetime
-
1998
- 1998-05-06 HK HK98103897A patent/HK1004754A1/xx not_active IP Right Cessation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1117771C (zh) * | 1997-04-29 | 2003-08-13 | 美国3M公司 | 键合的紫外光吸收剂 |
Also Published As
Publication number | Publication date |
---|---|
MX9206996A (es) | 1993-06-01 |
HK1004754A1 (en) | 1998-12-04 |
TW222293B (zh) | 1994-04-11 |
EP0545865A3 (en) | 1993-11-18 |
JP3113958B2 (ja) | 2000-12-04 |
KR930012927A (ko) | 1993-07-21 |
CA2084588C (en) | 2004-02-24 |
AU660203B2 (en) | 1995-06-15 |
ZA929420B (en) | 1993-06-07 |
CN1040007C (zh) | 1998-09-30 |
KR100259023B1 (ko) | 2000-06-15 |
AU2988292A (en) | 1993-06-10 |
CA2084588A1 (en) | 1993-06-07 |
JPH05320641A (ja) | 1993-12-03 |
CZ357292A3 (en) | 1993-09-15 |
RU2109027C1 (ru) | 1998-04-20 |
DE59205477D1 (de) | 1996-04-04 |
EP0545865A2 (de) | 1993-06-09 |
US5276258A (en) | 1994-01-04 |
BR9204852A (pt) | 1993-06-08 |
ES2084328T3 (es) | 1996-05-01 |
EP0545865B1 (de) | 1996-02-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1040007C (zh) | 稳定剂混合物 | |
DE69629971T2 (de) | Hammhemmende thermoplastische Harzzusammensetzung | |
CN1229427C (zh) | 含有氧化胺稳定剂组合物的聚合物组合物 | |
BE1011371A3 (fr) | Utilisation d'amino-uraciles substitues procede pour stabiliser du pvc rigide, composition ainsi obtenue et son utilisation. | |
CN1057545C (zh) | 回收的塑料混合物的稳定方法及其稳定剂混合物 | |
CN1057544C (zh) | 稳定单-材料的回收塑料的方法和该塑料的稳定剂混合物 | |
CN1214076C (zh) | 冲击强度改性剂、制造方法以及使用该改性剂的树脂组合物 | |
EP1960467A1 (de) | Polycarbonat-formmassen | |
EP1487914B1 (de) | Stabilisator-kombinationen für polymersysteme | |
EP2399959A1 (en) | Flame-retardant resin composition and molded article thereof | |
EP2556114B1 (de) | Flammgeschützte polycarbonat-zusammensetzungen | |
DE2418390A1 (de) | Phosphonat | |
CN1036275C (zh) | 3,9-双(1,2,2,6,6-五甲基-4-哌啶氧基)-2,4,8,10-四氧杂-3,0-,二磷杂螺环(5,5)十一烷在聚烯烃中作为稳定剂 | |
EP1846504A1 (de) | Polycarbonatformmassen mit verbesserter hydrolysebestaendigkeit | |
CN1425040A (zh) | 冲击强度改性剂及其制造方法和含该改性剂的热塑性树脂组合物 | |
CN1235974C (zh) | 阻燃聚碳酸酯树脂/abs接枝共聚物的共混物 | |
AU698316B2 (en) | Process for stabilising styrene-containing recycled plastic materials and stabiliser mixtures therefor | |
US3709884A (en) | 3,5-dialkyl-4-hydroxyphenyl alkanoic acid esters of 2,4,6-tris-(alkanolamino)derivatives of triazine | |
CN1663995A (zh) | 热塑性树脂组合物 | |
EP1214379B1 (de) | Flammwidrige polycarbonat-blends | |
JP3390101B2 (ja) | 滞留熱安定性に優れる熱可塑性樹脂組成物およびその製造方法 | |
EP1699859B1 (de) | Stabilisierte thermoplastische zusammensetzungen | |
DE2021088A1 (de) | Hydroxyalkylalkanoate und Hydroxyalkylbenzoate | |
JP2003020396A (ja) | 着色ポリカーボネート系難燃樹脂組成物及びその製造方法 | |
JPS61148287A (ja) | 抗酸化剤 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C15 | Extension of patent right duration from 15 to 20 years for appl. with date before 31.12.1992 and still valid on 11.12.2001 (patent law change 1993) | ||
OR01 | Other related matters | ||
C17 | Cessation of patent right | ||
CX01 | Expiry of patent term |
Expiration termination date: 20121205 Granted publication date: 19980930 |