JP3311405B2 - 安定化したポリオレフィンの製造方法およびそれにより得られる生成物 - Google Patents
安定化したポリオレフィンの製造方法およびそれにより得られる生成物Info
- Publication number
- JP3311405B2 JP3311405B2 JP35348092A JP35348092A JP3311405B2 JP 3311405 B2 JP3311405 B2 JP 3311405B2 JP 35348092 A JP35348092 A JP 35348092A JP 35348092 A JP35348092 A JP 35348092A JP 3311405 B2 JP3311405 B2 JP 3311405B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- butyl
- compound
- dimethoxypropane
- formula
- 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.)
- Expired - Fee Related
Links
- 238000000034 method Methods 0.000 title claims abstract description 52
- 229920000098 polyolefin Polymers 0.000 title claims abstract description 16
- 230000008569 process Effects 0.000 title claims abstract description 13
- 239000003381 stabilizer Substances 0.000 claims abstract description 56
- 239000003054 catalyst Substances 0.000 claims abstract description 44
- 150000001875 compounds Chemical class 0.000 claims abstract description 36
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 36
- -1 aluminum alkyl compound Chemical class 0.000 claims abstract description 30
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims abstract description 29
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000011949 solid catalyst Substances 0.000 claims abstract description 19
- 230000003647 oxidation Effects 0.000 claims abstract description 13
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 13
- 229910001629 magnesium chloride Inorganic materials 0.000 claims abstract description 12
- 239000007787 solid Substances 0.000 claims abstract description 10
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 7
- 239000000178 monomer Substances 0.000 claims abstract description 7
- 229920000642 polymer Polymers 0.000 claims description 46
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 15
- 125000003118 aryl group Chemical group 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 13
- 239000002245 particle Substances 0.000 claims description 10
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 9
- 238000012360 testing method Methods 0.000 claims description 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 8
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 6
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 6
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims description 6
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 5
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 4
- 125000000524 functional group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 229930195733 hydrocarbon Natural products 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 230000006698 induction Effects 0.000 claims description 3
- 239000004611 light stabiliser Substances 0.000 claims description 3
- 230000000379 polymerizing effect Effects 0.000 claims description 3
- 125000000923 (C1-C30) alkyl group Chemical group 0.000 claims description 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 150000003857 carboxamides Chemical class 0.000 claims description 2
- 230000009918 complex formation Effects 0.000 claims description 2
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000001033 ether group Chemical group 0.000 claims description 2
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 238000006467 substitution reaction Methods 0.000 claims description 2
- 150000002431 hydrogen Chemical group 0.000 claims 2
- 229920001384 propylene homopolymer Polymers 0.000 claims 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 238000002955 isolation Methods 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 abstract description 10
- IMNFDUFMRHMDMM-UHFFFAOYSA-N anhydrous n-heptane Natural products CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 9
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical group CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 7
- 150000001336 alkenes Chemical class 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000011777 magnesium Substances 0.000 description 6
- 230000000087 stabilizing effect Effects 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- BHPDSAAGSUWVMP-UHFFFAOYSA-N 3,3-bis(methoxymethyl)-2,6-dimethylheptane Chemical compound COCC(C(C)C)(COC)CCC(C)C BHPDSAAGSUWVMP-UHFFFAOYSA-N 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 4
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- PVWCLOAAEFMTLH-UHFFFAOYSA-N 4,4-bis(methoxymethyl)-2,6-dimethylheptane Chemical compound COCC(COC)(CC(C)C)CC(C)C PVWCLOAAEFMTLH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 150000002430 hydrocarbons Chemical group 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 239000002530 phenolic antioxidant Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 125000003386 piperidinyl group Chemical group 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000012798 spherical particle Substances 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 150000003609 titanium compounds Chemical class 0.000 description 3
- 238000004383 yellowing Methods 0.000 description 3
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- NGMVWDKVVMVTTM-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-3-methylbutane Chemical compound COCC(C(C)C)COC NGMVWDKVVMVTTM-UHFFFAOYSA-N 0.000 description 2
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 2
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 2
- SKWKIEFIPVHTHJ-UHFFFAOYSA-N 3,3-bis(methoxymethyl)pentane Chemical compound COCC(CC)(CC)COC SKWKIEFIPVHTHJ-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- ZVGIBQMBZHWERX-UHFFFAOYSA-N [2-(cyclohexylmethyl)-3-methoxy-2-(methoxymethyl)propyl]cyclohexane Chemical compound C1CCCCC1CC(COC)(COC)CC1CCCCC1 ZVGIBQMBZHWERX-UHFFFAOYSA-N 0.000 description 2
- HZDHNJUNAXAQNN-UHFFFAOYSA-N [C].N1CCCCC1 Chemical group [C].N1CCCCC1 HZDHNJUNAXAQNN-UHFFFAOYSA-N 0.000 description 2
- 125000003158 alcohol group Chemical group 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- AHUXYBVKTIBBJW-UHFFFAOYSA-N dimethoxy(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](OC)(OC)C1=CC=CC=C1 AHUXYBVKTIBBJW-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 150000003377 silicon compounds Chemical class 0.000 description 2
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- 238000001228 spectrum Methods 0.000 description 2
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- NOAIBMQZUGBONL-UHFFFAOYSA-N (1,3-dimethoxy-2-methylpropan-2-yl)benzene Chemical compound COCC(C)(COC)C1=CC=CC=C1 NOAIBMQZUGBONL-UHFFFAOYSA-N 0.000 description 1
- HPOWOWTVWZELDK-UHFFFAOYSA-N (1,3-dimethoxy-2-methylpropan-2-yl)cyclohexane Chemical compound COCC(C)(COC)C1CCCCC1 HPOWOWTVWZELDK-UHFFFAOYSA-N 0.000 description 1
- HBMODDNTUPGVFW-UHFFFAOYSA-N (1,3-dimethoxy-2-phenylpropan-2-yl)benzene Chemical compound C=1C=CC=CC=1C(COC)(COC)C1=CC=CC=C1 HBMODDNTUPGVFW-UHFFFAOYSA-N 0.000 description 1
- VAGULGJFHUPCET-UHFFFAOYSA-N (1,4-diethoxy-3-phenylbutan-2-yl)benzene Chemical compound C=1C=CC=CC=1C(COCC)C(COCC)C1=CC=CC=C1 VAGULGJFHUPCET-UHFFFAOYSA-N 0.000 description 1
- KGWNCXDKGBGRNE-UHFFFAOYSA-N (1,5-dimethoxy-4-phenylpentan-2-yl)benzene Chemical compound C=1C=CC=CC=1C(COC)CC(COC)C1=CC=CC=C1 KGWNCXDKGBGRNE-UHFFFAOYSA-N 0.000 description 1
- RUOIPKQBJXRXLF-UHFFFAOYSA-N (1,5-dimethoxy-5-phenylpentan-2-yl)benzene Chemical compound C=1C=CC=CC=1C(COC)CCC(OC)C1=CC=CC=C1 RUOIPKQBJXRXLF-UHFFFAOYSA-N 0.000 description 1
- NXDUWPUPBXRKTJ-UHFFFAOYSA-N (2-benzyl-1,3-dimethoxypropan-2-yl)benzene Chemical compound C=1C=CC=CC=1C(COC)(COC)CC1=CC=CC=C1 NXDUWPUPBXRKTJ-UHFFFAOYSA-N 0.000 description 1
- MEPSBRTXOHFWCF-UHFFFAOYSA-N (2-cyclohexyl-1,3-dimethoxypropan-2-yl)cyclohexane Chemical compound C1CCCCC1C(COC)(COC)C1CCCCC1 MEPSBRTXOHFWCF-UHFFFAOYSA-N 0.000 description 1
- USWVUBUQOUONFU-UHFFFAOYSA-N (3-cyclohexyl-1,4-diethoxybutan-2-yl)cyclohexane Chemical compound C1CCCCC1C(COCC)C(COCC)C1CCCCC1 USWVUBUQOUONFU-UHFFFAOYSA-N 0.000 description 1
- DCWBYZWJXUQBHC-UHFFFAOYSA-N (3-cyclohexyl-1,4-dimethoxybutan-2-yl)cyclohexane Chemical compound C1CCCCC1C(COC)C(COC)C1CCCCC1 DCWBYZWJXUQBHC-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
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- WJLFNLNAXRVNGL-UHFFFAOYSA-N 1,1-bis(methoxymethyl)cyclohexane Chemical compound COCC1(COC)CCCCC1 WJLFNLNAXRVNGL-UHFFFAOYSA-N 0.000 description 1
- JSBYVJZYWNPFLQ-UHFFFAOYSA-N 1,1-bis(methoxymethyl)cyclopentane Chemical compound COCC1(COC)CCCC1 JSBYVJZYWNPFLQ-UHFFFAOYSA-N 0.000 description 1
- NQPBSRVXHWBUAO-UHFFFAOYSA-N 1,1-bis(methoxymethyl)cyclopropane Chemical compound COCC1(COC)CC1 NQPBSRVXHWBUAO-UHFFFAOYSA-N 0.000 description 1
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- KMHHDYHFTHLDOP-UHFFFAOYSA-N 1,2-bis(methoxymethyl)-4-methyl-1-propan-2-ylcyclohexane Chemical compound COCC1CC(C)CCC1(COC)C(C)C KMHHDYHFTHLDOP-UHFFFAOYSA-N 0.000 description 1
- GYQJEHJHOZYHIM-UHFFFAOYSA-N 1,2-bis(methoxymethyl)cyclohexane Chemical compound COCC1CCCCC1COC GYQJEHJHOZYHIM-UHFFFAOYSA-N 0.000 description 1
- HYKQSAMEQTXOBX-UHFFFAOYSA-N 1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan Chemical compound C1OCC2COCC21 HYKQSAMEQTXOBX-UHFFFAOYSA-N 0.000 description 1
- PTOOVEFBMMTMJP-UHFFFAOYSA-N 1,3-dimethoxy-2-(methoxymethyl)-2-methylpropane Chemical compound COCC(C)(COC)COC PTOOVEFBMMTMJP-UHFFFAOYSA-N 0.000 description 1
- CELOJHLXFPSJPH-UHFFFAOYSA-N 1,3-dimethoxypropan-2-ylbenzene Chemical compound COCC(COC)C1=CC=CC=C1 CELOJHLXFPSJPH-UHFFFAOYSA-N 0.000 description 1
- NOWCPSTWMDNKTI-UHFFFAOYSA-N 1,3-dimethoxypropan-2-ylcyclohexane Chemical compound COCC(COC)C1CCCCC1 NOWCPSTWMDNKTI-UHFFFAOYSA-N 0.000 description 1
- UUAMLBIYJDPGFU-UHFFFAOYSA-N 1,3-dimethoxypropane Chemical compound COCCCOC UUAMLBIYJDPGFU-UHFFFAOYSA-N 0.000 description 1
- PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 1
- YDGNDCHPLHXQMK-UHFFFAOYSA-N 1-(1,3-dimethoxypropan-2-yl)-1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalene Chemical compound C1CCCC2C(C(COC)COC)CCCC21 YDGNDCHPLHXQMK-UHFFFAOYSA-N 0.000 description 1
- ZTVGJMMXVMDFCX-UHFFFAOYSA-N 1-[1,3-dimethoxy-2-(4-methylphenyl)propan-2-yl]-4-methylbenzene Chemical compound C=1C=C(C)C=CC=1C(COC)(COC)C1=CC=C(C)C=C1 ZTVGJMMXVMDFCX-UHFFFAOYSA-N 0.000 description 1
- AXRFHUBGMFVHNO-UHFFFAOYSA-N 1-[1,4-dimethoxy-2-(4-methylphenyl)butan-2-yl]-4-methylbenzene Chemical compound C=1C=C(C)C=CC=1C(COC)(CCOC)C1=CC=C(C)C=C1 AXRFHUBGMFVHNO-UHFFFAOYSA-N 0.000 description 1
- HZCHNISPTTWXMO-UHFFFAOYSA-N 1-[2-(2,2-dimethylpropoxy)ethoxy]-2,2-dimethylpropane Chemical compound CC(C)(C)COCCOCC(C)(C)C HZCHNISPTTWXMO-UHFFFAOYSA-N 0.000 description 1
- KDFJWFAVQBAPSO-UHFFFAOYSA-N 1-[3-(2,2-dimethylpropoxy)propoxy]-2,2-dimethylpropane Chemical compound CC(C)(C)COCCCOCC(C)(C)C KDFJWFAVQBAPSO-UHFFFAOYSA-N 0.000 description 1
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
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- 239000011261 inert gas Substances 0.000 description 1
- 238000010813 internal standard method Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- YTXCAJNHPVBVDJ-UHFFFAOYSA-N octadecyl propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CC YTXCAJNHPVBVDJ-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 238000012667 polymer degradation Methods 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 125000006839 xylylene group Chemical group 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerisation Methods In General (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Laminated Bodies (AREA)
- Fluid-Damping Devices (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT191A003346 | 1991-12-13 | ||
| ITMI913346A IT1252205B (it) | 1991-12-13 | 1991-12-13 | Processo per la preparazione di poliolefine stabilizzate e prodotti cosi` ottenuti. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05271335A JPH05271335A (ja) | 1993-10-19 |
| JP3311405B2 true JP3311405B2 (ja) | 2002-08-05 |
Family
ID=11361329
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP35348092A Expired - Fee Related JP3311405B2 (ja) | 1991-12-13 | 1992-12-14 | 安定化したポリオレフィンの製造方法およびそれにより得られる生成物 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US5278210A (en:Method) |
| EP (1) | EP0546573B1 (en:Method) |
| JP (1) | JP3311405B2 (en:Method) |
| KR (1) | KR100258489B1 (en:Method) |
| CN (1) | CN1035385C (en:Method) |
| AT (1) | ATE163944T1 (en:Method) |
| AU (1) | AU657379B2 (en:Method) |
| BR (1) | BR9204981A (en:Method) |
| CA (1) | CA2085194A1 (en:Method) |
| DE (1) | DE69224711T2 (en:Method) |
| ES (1) | ES2114905T3 (en:Method) |
| FI (1) | FI105819B (en:Method) |
| IT (1) | IT1252205B (en:Method) |
| NO (1) | NO301123B1 (en:Method) |
| RU (1) | RU2070206C1 (en:Method) |
| TW (1) | TW239151B (en:Method) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1255233B (it) * | 1992-07-17 | 1995-10-20 | Himont Inc | Procedimento per la stabilizzazione di polimeri olefinici |
| IT1264679B1 (it) * | 1993-07-07 | 1996-10-04 | Spherilene Srl | Catalizzatori per la (co)polimerizzazione di etilene |
| US5646207A (en) * | 1994-03-14 | 1997-07-08 | Ppg Industries, Inc. | Aqueous sizing compositions for glass fibers providing improved whiteness in glass fiber reinforced plastics |
| CN1068338C (zh) * | 1994-08-29 | 2001-07-11 | 中国石化扬子石油化工公司 | 一种α-烯烃的聚合方法 |
| CN1232472A (zh) * | 1996-09-04 | 1999-10-20 | 陶氏化学公司 | 在聚烯烃中加入自由基抑制剂 |
| US5948720A (en) * | 1997-01-07 | 1999-09-07 | Huntsman Polymers Corporation | Catalyst for the production of flexible polyolefin compositions, methods for making and using same, and products thereof |
| RU2196782C2 (ru) * | 2001-03-15 | 2003-01-20 | Институт нефтехимического синтеза им. А.В.Топчиева РАН | Способ получения синтетической гуттаперчи (варианты) |
| US6777470B2 (en) * | 2001-05-29 | 2004-08-17 | Sunoco, Inc. (R&M) | Polyolefin additive packages for producing articles with enhanced stain resistance |
| ES2289295T3 (es) * | 2002-06-13 | 2008-02-01 | Basell Poliolefine Italia S.R.L. | Componentes cataliticos ziegler natta para la polimerizacion de olefinas. |
| JP4969070B2 (ja) | 2005-03-11 | 2012-07-04 | 株式会社Ａｄｅｋａ | 安定化されたポリマーの製造方法 |
| PL2225288T3 (pl) * | 2007-12-21 | 2019-01-31 | W.R. Grace & Co. - Conn. | Samograniczajca się kompozycja katalizatora z wewnętrznym donorem dwufunkcyjnym |
| EP2281825A4 (en) * | 2008-06-05 | 2012-02-22 | Adeka Corp | ALUMINUM OXIDE AND METHOD FOR PRODUCING STABILIZED POLYMERS USING ALUMINUM OXIDE |
| CN102131766B (zh) * | 2008-08-25 | 2013-12-11 | 杜邦电子聚合物公司 | 丙酸酯和其制备方法 |
| DE102009023651B4 (de) * | 2009-05-26 | 2021-07-01 | Aesculap Ag | Verfahren zur Herstellung eines mit einem Stabilisator dotierten Polyethylens und Verwendung eines nach diesem Verfahren hergestellten Polyethylens |
| KR101739306B1 (ko) | 2009-09-04 | 2017-05-24 | 가부시키가이샤 아데카 | 페놀계 산화 방지제의 재생 방법, 올레핀 중합체의 제조 방법, 폴리올레핀 파우더, 및 섬유 |
| JP5710186B2 (ja) | 2010-09-10 | 2015-04-30 | 株式会社Adeka | 安定化ポリマーの製造方法 |
| KR102115865B1 (ko) | 2010-11-16 | 2020-05-27 | 가부시키가이샤 아데카 | 폴리머의 장기 안정화 방법 및 부직포, 일래스터머 조성물의 제조 방법 |
| BR112016008951B1 (pt) | 2013-10-21 | 2021-11-03 | Adeka Corporation | Método para produção de polímero estabilizado |
| JP6909594B2 (ja) | 2017-03-03 | 2021-07-28 | 株式会社Adeka | 安定化されたオレフィン系樹脂組成物の製造方法 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3477991A (en) * | 1968-06-05 | 1969-11-11 | Exxon Research Engineering Co | Alkenyl hindered phenol and a copolymer of an alkenyl phenol and a monoolefin |
| IT1096661B (it) * | 1978-06-13 | 1985-08-26 | Montedison Spa | Procedimento per la preparazione di prodotti in forma sferoidale solidi a temperatura ambiente |
| DE2841645A1 (de) * | 1978-09-25 | 1980-04-03 | Basf Ag | Verfahren zum herstellen von homo- und copolymerisaten von alpha -monoolefinen |
| IT1207491B (it) * | 1985-01-30 | 1989-05-25 | Himont Inc | Procedimento per preparare polimeri olefinici, termicamente stabili. |
| US4960593A (en) * | 1985-01-30 | 1990-10-02 | Hilmont Incorporated | Process for preparing thermally stable olefinic polymers |
| GB2183244B (en) * | 1985-11-26 | 1989-11-15 | Toho Titanium Co Ltd | Olefin-polymerization catalysts and component therefor |
| IT1213312B (it) * | 1986-07-30 | 1989-12-20 | Enichem Sintesi | Procedimento di (co)polimerizzazioni di alfa olefine in presenta di stabilizzanti. |
| IT1196980B (it) * | 1986-07-23 | 1988-11-25 | Enichem Sintesi | Procedimento di (co)polimerizzazione di alfa-olefine in presenza di antiossidanti |
| IT1197320B (it) * | 1986-10-02 | 1988-11-30 | Ausimont Spa | Catalizzatori per la preparazione di copolimeri olefinici elastomerici,saturi ed insaturi,e vopolimeri con essi ottenuti |
| US4818799A (en) * | 1987-11-13 | 1989-04-04 | Shell Oil Company | Process for the in-reactor stabilization of polyolefins |
| US4879141A (en) * | 1988-01-25 | 1989-11-07 | Shell Oil Company | In-reactor stabilization of polyolefins via coated stabilizers |
| US5045577A (en) * | 1988-06-30 | 1991-09-03 | Ciba-Geigy Corporation | Process for the preparation of heat-stable olefin polymers |
| EP0350444A1 (de) * | 1988-06-30 | 1990-01-10 | Ciba-Geigy Ag | Verfahren zum Stabilisieren von Polyolefinen |
| IT1227258B (it) * | 1988-09-30 | 1991-03-28 | Himont Inc | Componenti e catalizzatori per la polimerizzazione di olefine |
| US5064878A (en) * | 1989-07-05 | 1991-11-12 | Shell Oil Company | In-reactor stabilization of polymers via coated stabilizers |
| EP0439622A4 (en) * | 1989-08-18 | 1993-05-26 | Tonen Corporation | Catalytic component for alpha-olefin polymerization |
| IT1241062B (it) * | 1990-01-10 | 1993-12-29 | Himont Inc | Componenti e catalizzatori per la polimerizzazione di olefine |
-
1991
- 1991-12-13 IT ITMI913346A patent/IT1252205B/it active IP Right Grant
-
1992
- 1992-12-09 AU AU30013/92A patent/AU657379B2/en not_active Ceased
- 1992-12-10 BR BR9204981A patent/BR9204981A/pt not_active Application Discontinuation
- 1992-12-10 US US07/988,646 patent/US5278210A/en not_active Expired - Lifetime
- 1992-12-10 TW TW081109885A patent/TW239151B/zh active
- 1992-12-11 DE DE69224711T patent/DE69224711T2/de not_active Expired - Fee Related
- 1992-12-11 NO NO924795A patent/NO301123B1/no not_active IP Right Cessation
- 1992-12-11 CA CA002085194A patent/CA2085194A1/en not_active Abandoned
- 1992-12-11 FI FI925637A patent/FI105819B/fi active
- 1992-12-11 EP EP92121170A patent/EP0546573B1/en not_active Expired - Lifetime
- 1992-12-11 AT AT92121170T patent/ATE163944T1/de not_active IP Right Cessation
- 1992-12-11 ES ES92121170T patent/ES2114905T3/es not_active Expired - Lifetime
- 1992-12-11 RU RU9292004528A patent/RU2070206C1/ru active
- 1992-12-12 CN CN92115246.9A patent/CN1035385C/zh not_active Expired - Fee Related
- 1992-12-12 KR KR1019920024092A patent/KR100258489B1/ko not_active Expired - Fee Related
- 1992-12-14 JP JP35348092A patent/JP3311405B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CN1035385C (zh) | 1997-07-09 |
| DE69224711T2 (de) | 1998-09-24 |
| IT1252205B (it) | 1995-06-05 |
| ITMI913346A0 (it) | 1991-12-13 |
| NO924795L (no) | 1993-06-14 |
| ATE163944T1 (de) | 1998-03-15 |
| JPH05271335A (ja) | 1993-10-19 |
| AU3001392A (en) | 1993-06-17 |
| BR9204981A (pt) | 1993-06-15 |
| ES2114905T3 (es) | 1998-06-16 |
| FI925637L (fi) | 1993-06-14 |
| EP0546573A1 (en) | 1993-06-16 |
| US5278210A (en) | 1994-01-11 |
| NO924795D0 (no) | 1992-12-11 |
| CA2085194A1 (en) | 1993-06-14 |
| ITMI913346A1 (it) | 1993-06-13 |
| CN1074222A (zh) | 1993-07-14 |
| DE69224711D1 (de) | 1998-04-16 |
| AU657379B2 (en) | 1995-03-09 |
| RU2070206C1 (ru) | 1996-12-10 |
| EP0546573B1 (en) | 1998-03-11 |
| FI105819B (fi) | 2000-10-13 |
| KR100258489B1 (ko) | 2000-06-15 |
| TW239151B (en:Method) | 1995-01-21 |
| NO301123B1 (no) | 1997-09-15 |
| FI925637A0 (fi) | 1992-12-11 |
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