ES2626363T3 - Película con bajo índice de gel OCS - Google Patents
Película con bajo índice de gel OCS Download PDFInfo
- Publication number
- ES2626363T3 ES2626363T3 ES13739223.9T ES13739223T ES2626363T3 ES 2626363 T3 ES2626363 T3 ES 2626363T3 ES 13739223 T ES13739223 T ES 13739223T ES 2626363 T3 ES2626363 T3 ES 2626363T3
- Authority
- ES
- Spain
- Prior art keywords
- polypropylene
- agents
- melt
- molten state
- extensibility
- 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.)
- Active
Links
- 239000004743 Polypropylene Substances 0.000 claims abstract description 531
- 229920001155 polypropylene Polymers 0.000 claims abstract description 493
- -1 polypropylene Polymers 0.000 claims abstract description 429
- 239000000155 melt Substances 0.000 claims abstract description 123
- 239000000203 mixture Substances 0.000 claims abstract description 120
- 239000000654 additive Substances 0.000 claims abstract description 66
- 101100023124 Schizosaccharomyces pombe (strain 972 / ATCC 24843) mfr2 gene Proteins 0.000 claims abstract description 57
- 229920000642 polymer Polymers 0.000 claims abstract description 56
- 239000000178 monomer Substances 0.000 claims abstract description 54
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 44
- 238000000034 method Methods 0.000 claims abstract description 44
- 150000003254 radicals Chemical class 0.000 claims abstract description 26
- 230000000996 additive effect Effects 0.000 claims abstract description 19
- 239000002245 particle Substances 0.000 claims abstract description 19
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 13
- 238000009826 distribution Methods 0.000 claims abstract description 13
- 239000002253 acid Substances 0.000 claims abstract description 10
- 239000004604 Blowing Agent Substances 0.000 claims abstract description 9
- 239000012963 UV stabilizer Substances 0.000 claims abstract description 9
- 239000002981 blocking agent Substances 0.000 claims abstract description 9
- 239000000314 lubricant Substances 0.000 claims abstract description 9
- 239000006078 metal deactivator Substances 0.000 claims abstract description 9
- 239000002216 antistatic agent Substances 0.000 claims abstract description 7
- 239000002667 nucleating agent Substances 0.000 claims abstract description 7
- 230000001464 adherent effect Effects 0.000 claims abstract description 6
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 42
- 238000002156 mixing Methods 0.000 claims description 27
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 26
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 19
- 238000005979 thermal decomposition reaction Methods 0.000 claims description 16
- 150000002978 peroxides Chemical group 0.000 claims description 15
- 238000005482 strain hardening Methods 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 239000012748 slip agent Substances 0.000 claims description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
- 239000007767 bonding agent Substances 0.000 claims description 3
- 150000001993 dienes Chemical class 0.000 claims description 3
- 229920001519 homopolymer Polymers 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 description 23
- 238000004519 manufacturing process Methods 0.000 description 14
- 229920001384 propylene homopolymer Polymers 0.000 description 12
- 238000002844 melting Methods 0.000 description 11
- 230000008018 melting Effects 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 8
- 239000005977 Ethylene Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 238000005259 measurement Methods 0.000 description 8
- 239000001993 wax Substances 0.000 description 8
- 239000000843 powder Substances 0.000 description 7
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 7
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 6
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 238000001228 spectrum Methods 0.000 description 6
- 238000007385 chemical modification Methods 0.000 description 5
- 238000002425 crystallisation Methods 0.000 description 5
- 230000008025 crystallization Effects 0.000 description 5
- 230000007547 defect Effects 0.000 description 5
- 238000001125 extrusion Methods 0.000 description 5
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 206010065042 Immune reconstitution inflammatory syndrome Diseases 0.000 description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- 229920005601 base polymer Polymers 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 4
- 230000004927 fusion Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229920002857 polybutadiene Polymers 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- SDJHPPZKZZWAKF-UHFFFAOYSA-N 2,3-dimethylbuta-1,3-diene Chemical compound CC(=C)C(C)=C SDJHPPZKZZWAKF-UHFFFAOYSA-N 0.000 description 3
- 239000005062 Polybutadiene Substances 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 230000001133 acceleration Effects 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 229920001038 ethylene copolymer Polymers 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- KDGNCLDCOVTOCS-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy propan-2-yl carbonate Chemical compound CC(C)OC(=O)OOC(C)(C)C KDGNCLDCOVTOCS-UHFFFAOYSA-N 0.000 description 2
- HCILJBJJZALOAL-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)-n'-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyl]propanehydrazide Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)NNC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 HCILJBJJZALOAL-UHFFFAOYSA-N 0.000 description 2
- UAUDZVJPLUQNMU-UHFFFAOYSA-N Erucasaeureamid Natural products CCCCCCCCC=CCCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000011954 Ziegler–Natta catalyst Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 229920000554 ionomer Polymers 0.000 description 2
- 239000004611 light stabiliser Substances 0.000 description 2
- JGMMIGGLIIRHFV-UHFFFAOYSA-N nonane-1,2,3,4,5,6,7,8,9-nonol Chemical compound OCC(O)C(O)C(O)C(O)C(O)C(O)C(O)CO JGMMIGGLIIRHFV-UHFFFAOYSA-N 0.000 description 2
- 230000006911 nucleation Effects 0.000 description 2
- 238000010899 nucleation Methods 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 2
- FATBGEAMYMYZAF-UHFFFAOYSA-N oleicacidamide-heptaglycolether Natural products CCCCCCCCC=CCCCCCCCC(N)=O FATBGEAMYMYZAF-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 235000019809 paraffin wax Nutrition 0.000 description 2
- 150000002976 peresters Chemical class 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 2
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000002516 radical scavenger Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 238000000518 rheometry Methods 0.000 description 2
- 235000010356 sorbitol Nutrition 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- OTNBTDJNEBMLOV-UHFFFAOYSA-N (1-tert-butylcyclohexyl)oxy formate Chemical compound O=COOC1(C(C)(C)C)CCCCC1 OTNBTDJNEBMLOV-UHFFFAOYSA-N 0.000 description 1
- MYOQALXKVOJACM-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy pentaneperoxoate Chemical compound CCCCC(=O)OOOC(C)(C)C MYOQALXKVOJACM-UHFFFAOYSA-N 0.000 description 1
- FHPGGLFJNIYWLK-UHFFFAOYSA-N (3-tert-butyl-2-nitrophenyl) carbamoperoxoate Chemical compound CC(C)(C)C1=CC=CC(OOC(N)=O)=C1[N+]([O-])=O FHPGGLFJNIYWLK-UHFFFAOYSA-N 0.000 description 1
- OGQVROWWFUXRST-FNORWQNLSA-N (3e)-hepta-1,3-diene Chemical compound CCC\C=C\C=C OGQVROWWFUXRST-FNORWQNLSA-N 0.000 description 1
- IMYCVFRTNVMHAD-UHFFFAOYSA-N 1,1-bis(2-methylbutan-2-ylperoxy)cyclohexane Chemical compound CCC(C)(C)OOC1(OOC(C)(C)CC)CCCCC1 IMYCVFRTNVMHAD-UHFFFAOYSA-N 0.000 description 1
- NALFRYPTRXKZPN-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane Chemical compound CC1CC(C)(C)CC(OOC(C)(C)C)(OOC(C)(C)C)C1 NALFRYPTRXKZPN-UHFFFAOYSA-N 0.000 description 1
- PRJNEUBECVAVAG-UHFFFAOYSA-N 1,3-bis(ethenyl)benzene Chemical compound C=CC1=CC=CC(C=C)=C1 PRJNEUBECVAVAG-UHFFFAOYSA-N 0.000 description 1
- WEERVPDNCOGWJF-UHFFFAOYSA-N 1,4-bis(ethenyl)benzene Chemical compound C=CC1=CC=C(C=C)C=C1 WEERVPDNCOGWJF-UHFFFAOYSA-N 0.000 description 1
- 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 1
- NPRFVBVVQXZPOO-UHFFFAOYSA-N 1-tert-butylcyclohexane-1-carboxylic acid Chemical compound CC(C)(C)C1(C(O)=O)CCCCC1 NPRFVBVVQXZPOO-UHFFFAOYSA-N 0.000 description 1
- WMEKVVUBQYGKMS-UHFFFAOYSA-N 1-tert-butylperoxy-n,n-dimethylmethanamine Chemical compound CN(C)COOC(C)(C)C WMEKVVUBQYGKMS-UHFFFAOYSA-N 0.000 description 1
- GOAHRBQLKIZLKG-UHFFFAOYSA-N 1-tert-butylperoxybutane Chemical compound CCCCOOC(C)(C)C GOAHRBQLKIZLKG-UHFFFAOYSA-N 0.000 description 1
- GGHLNAHECMSTCO-UHFFFAOYSA-N 2,2-diphenylethenyl benzenecarboperoxoate Chemical compound C=1C=CC=CC=1C(=O)OOC=C(C=1C=CC=CC=1)C1=CC=CC=C1 GGHLNAHECMSTCO-UHFFFAOYSA-N 0.000 description 1
- LQAWFRMAGBHXKF-UHFFFAOYSA-N 2,4-dimethylpentan-2-ylperoxy hydrogen carbonate Chemical compound CC(C)CC(C)(C)OOOC(O)=O LQAWFRMAGBHXKF-UHFFFAOYSA-N 0.000 description 1
- JJRDRFZYKKFYMO-UHFFFAOYSA-N 2-methyl-2-(2-methylbutan-2-ylperoxy)butane Chemical compound CCC(C)(C)OOC(C)(C)CC JJRDRFZYKKFYMO-UHFFFAOYSA-N 0.000 description 1
- RQQWRNIJMXXFMI-UHFFFAOYSA-N 2-methyl-2-prop-2-enylperoxypropane Chemical compound CC(C)(C)OOCC=C RQQWRNIJMXXFMI-UHFFFAOYSA-N 0.000 description 1
- GAMCAFSVFAIDDB-UHFFFAOYSA-N 2-phenylethyl 2-nitrobenzenecarboperoxoate Chemical compound [O-][N+](=O)C1=CC=CC=C1C(=O)OOCCC1=CC=CC=C1 GAMCAFSVFAIDDB-UHFFFAOYSA-N 0.000 description 1
- BIISIZOQPWZPPS-UHFFFAOYSA-N 2-tert-butylperoxypropan-2-ylbenzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC=C1 BIISIZOQPWZPPS-UHFFFAOYSA-N 0.000 description 1
- XAXYTHWQHBSHRO-UHFFFAOYSA-N 3,3-diethylpenta-1,4-diene Chemical compound CCC(CC)(C=C)C=C XAXYTHWQHBSHRO-UHFFFAOYSA-N 0.000 description 1
- BHZUNHXTRRNKST-UHFFFAOYSA-N 3,3-dimethylpenta-1,4-diene Chemical compound C=CC(C)(C)C=C BHZUNHXTRRNKST-UHFFFAOYSA-N 0.000 description 1
- DPVURGVGKNKMOH-UHFFFAOYSA-N 3-[3-(aminomethyl)-3-ethyl-2-methylpentan-2-yl]peroxy-2,2-diethyl-3-methylbutan-1-amine Chemical compound CCC(CC)(CN)C(C)(C)OOC(C)(C)C(CC)(CC)CN DPVURGVGKNKMOH-UHFFFAOYSA-N 0.000 description 1
- ZXABMDQSAABDMG-UHFFFAOYSA-N 3-ethenoxyprop-1-ene Chemical compound C=CCOC=C ZXABMDQSAABDMG-UHFFFAOYSA-N 0.000 description 1
- HLNLZCCXNOLUIS-UHFFFAOYSA-N 4-butylperoxybutan-1-ol Chemical compound CCCCOOCCCCO HLNLZCCXNOLUIS-UHFFFAOYSA-N 0.000 description 1
- KKAPQNYTVKOCIP-UHFFFAOYSA-N 4-tert-butylbicyclo[2.2.1]heptane Chemical compound C1CC2CCC1(C(C)(C)C)C2 KKAPQNYTVKOCIP-UHFFFAOYSA-N 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 101100533229 Galleria mellonella SER1 gene Proteins 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- 241001122767 Theaceae Species 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 1
- CJSBUWDGPXGFGA-UHFFFAOYSA-N dimethyl-butadiene Natural products CC(C)=CC=C CJSBUWDGPXGFGA-UHFFFAOYSA-N 0.000 description 1
- 229920006379 extruded polypropylene Polymers 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- AHAREKHAZNPPMI-UHFFFAOYSA-N hexa-1,3-diene Chemical compound CCC=CC=C AHAREKHAZNPPMI-UHFFFAOYSA-N 0.000 description 1
- 229960001545 hydrotalcite Drugs 0.000 description 1
- 229910001701 hydrotalcite Inorganic materials 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 238000006011 modification reaction Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- NZPFUDSAKCRWLC-UHFFFAOYSA-N n,n-dimethyl-1-(2-methylbutan-2-ylperoxy)methanamine Chemical compound CCC(C)(C)OOCN(C)C NZPFUDSAKCRWLC-UHFFFAOYSA-N 0.000 description 1
- HZSIAIOCKWAYMD-UHFFFAOYSA-N n-(2-methylbutan-2-ylperoxymethyl)-n-propan-2-ylpropan-2-amine Chemical compound CCC(C)(C)OOCN(C(C)C)C(C)C HZSIAIOCKWAYMD-UHFFFAOYSA-N 0.000 description 1
- MMCOUVMKNAHQOY-UHFFFAOYSA-L oxido carbonate Chemical compound [O-]OC([O-])=O MMCOUVMKNAHQOY-UHFFFAOYSA-L 0.000 description 1
- QYZLKGVUSQXAMU-UHFFFAOYSA-N penta-1,4-diene Chemical compound C=CCC=C QYZLKGVUSQXAMU-UHFFFAOYSA-N 0.000 description 1
- 150000004978 peroxycarbonates Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920005629 polypropylene homopolymer Polymers 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000005029 sieve analysis Methods 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- PFBLRDXPNUJYJM-UHFFFAOYSA-N tert-butyl 2-methylpropaneperoxoate Chemical compound CC(C)C(=O)OOC(C)(C)C PFBLRDXPNUJYJM-UHFFFAOYSA-N 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- BONXXHJNJLHEDZ-UHFFFAOYSA-N tert-butylcyclobutane Chemical compound CC(C)(C)C1CCC1 BONXXHJNJLHEDZ-UHFFFAOYSA-N 0.000 description 1
- CJKIVLPJDVFXJP-UHFFFAOYSA-N tert-butylcyclopropane Chemical compound CC(C)(C)C1CC1 CJKIVLPJDVFXJP-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/14—Copolymers of propene
- C08L23/142—Copolymers of propene at least partially crystalline copolymers of propene with other olefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/06—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- 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
- C08F10/04—Monomers containing three or four carbon atoms
- C08F10/06—Propene
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/52—Polymerisation initiated by wave energy or particle radiation by electric discharge, e.g. voltolisation
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/54—Polymerisation initiated by wave energy or particle radiation by X-rays or electrons
-
- 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
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/04—Monomers containing three or four carbon atoms
- C08F210/06—Propene
-
- 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
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
-
- 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
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
-
- 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
- C08K5/10—Esters; Ether-esters
- C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/12—Polypropene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2351/00—Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
- C08J2351/06—Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/26—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
- C08L2023/40—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment by reaction with compounds changing molecular weight
- C08L2023/42—Depolymerisation, vis-breaking or degradation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/16—Applications used for films
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2207/00—Properties characterising the ingredient of the composition
- C08L2207/06—Properties of polyethylene
- C08L2207/07—Long chain branching
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Crystallography & Structural Chemistry (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12177878 | 2012-07-25 | ||
| EP12177878 | 2012-07-25 | ||
| PCT/EP2013/065263 WO2014016206A1 (en) | 2012-07-25 | 2013-07-19 | Film with low ocs gel index |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2626363T3 true ES2626363T3 (es) | 2017-07-24 |
Family
ID=48803558
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES13739223.9T Active ES2626363T3 (es) | 2012-07-25 | 2013-07-19 | Película con bajo índice de gel OCS |
Country Status (11)
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR112015000935A2 (pt) * | 2012-07-25 | 2017-06-27 | Borealis Ag | espuma produzida a partir de polipropileno com baixo conteúdo de gel |
| ES2574437T3 (es) | 2013-06-05 | 2016-06-17 | Borealis Ag | Producción en una etapa de una composición de polipropileno |
| ES2724243T3 (es) | 2014-11-05 | 2019-09-09 | Borealis Ag | Polipropileno ramificado de cadena larga para aplicación de espuma |
| EP3018156B1 (en) * | 2014-11-05 | 2023-03-22 | Borealis AG | Branched polypropylene for foam applications |
| ES2717433T3 (es) * | 2014-11-05 | 2019-06-21 | Borealis Ag | Polipropileno ramificado de cadena larga para la aplicación en películas |
| CN107848222B (zh) * | 2015-02-04 | 2019-08-27 | 博里利斯股份公司 | 在挤出机中制备改性烯烃聚合物的方法 |
| EP3280748B1 (en) * | 2015-04-10 | 2021-07-14 | Borealis AG | Process for mixing olefin polymer with reactants |
| CN107709008A (zh) | 2015-08-13 | 2018-02-16 | 埃克森美孚化学专利公司 | 含高熔体强度聚丙烯的多层片材 |
| BR112018006475B1 (pt) * | 2015-10-21 | 2022-03-15 | Borealis Ag | Composição de polipropileno ramificado de cadeia longa, processos para produzir uma composição de polipropileno ramificado de cadeia longa, para produzir um artigo e uma espuma, artigo, espuma ou um artigo espumado, e, uso de uma composição de polipropileno ramificado de cadeia longa |
| EP3450489B1 (en) * | 2016-08-18 | 2024-10-09 | Japan Polypropylene Corporation | Microporous film comprising a polypropylene resin composition |
| ES2873506T3 (es) | 2016-12-09 | 2021-11-03 | Borealis Ag | Composición de polipropileno para aplicaciones de espuma |
| TWI659824B (zh) * | 2016-12-30 | 2019-05-21 | 奧地利商柏列利斯股份公司 | 低排放聚丙烯發泡片材 |
| KR102257918B1 (ko) * | 2017-02-07 | 2021-05-27 | 엑손모빌 케미칼 패턴츠 인코포레이티드 | 개선된 가공성을 갖는 고 용융 강도 폴리프로필렌 |
| WO2018147944A1 (en) * | 2017-02-07 | 2018-08-16 | Exxonmobil Chemical Patents Inc. | High melt strength polypropylenes with improved processability |
| KR102420733B1 (ko) | 2017-07-13 | 2022-07-15 | 엑손모빌 케미칼 패턴츠 인코포레이티드 | 변형률 경화된 폴리프로필렌의 제조 방법 |
| WO2019059222A1 (ja) * | 2017-09-21 | 2019-03-28 | 株式会社Ｔｂｍ | 熱可塑性樹脂組成物およびこれを用いてなる成形品 |
| ES2974283T3 (es) * | 2017-10-25 | 2024-06-26 | Borealis Ag | Composición de polipropileno cargado con propiedades termo-mecánicas mejoradas |
| WO2020231526A1 (en) | 2019-05-15 | 2020-11-19 | Exxonmobil Chemical Patents Inc. | Polypropylene-based compositions |
| EP3994186A1 (en) * | 2019-07-04 | 2022-05-11 | Borealis AG | Long-chain branched propylene polymer composition |
| EP4172253A1 (en) * | 2020-06-26 | 2023-05-03 | Borealis AG | Polypropylene composition for hms pp foam sheet with balanced bending resistance |
| HUE065425T2 (hu) | 2021-04-01 | 2024-05-28 | Borealis Ag | Filmek készítésére alkalmas polimer összetétel |
| CN114058115B (zh) * | 2021-08-31 | 2023-06-06 | 成都金发科技新材料有限公司 | 一种抗菌抗病毒高冲击聚丙烯组合物及其制备方法和应用 |
| WO2024038070A1 (en) * | 2022-08-19 | 2024-02-22 | Borealis Ag | Process for preparing a long chain branched polypropylene composition |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4957968A (en) * | 1988-08-09 | 1990-09-18 | Monsanto Company | Adhesive thermoplastic elastomer blends |
| EP0787750B1 (de) | 1996-02-01 | 2003-05-14 | Borealis GmbH | Strukturisomere Poly(alkylethylene) |
| JPH09309966A (ja) | 1996-05-23 | 1997-12-02 | Kanegafuchi Chem Ind Co Ltd | 改質ポリプロピレン系樹脂組成物からなる発泡体 |
| US6087431A (en) | 1997-04-14 | 2000-07-11 | Asahi Kasei Kagyo Kabushiki Kaisha | Olefinic thermoplastic elastomer composition |
| US6204348B1 (en) | 1997-05-20 | 2001-03-20 | Borealis Gmbh | Modified polypropylenes of improved processability |
| US6077907A (en) | 1997-07-09 | 2000-06-20 | Borealis Ag | Molded polyolefin parts of improved dimensional stability at elevated temperatures and improved stiffness |
| JPH11302425A (ja) | 1998-04-21 | 1999-11-02 | Sekisui Chem Co Ltd | 流動性を有する発泡性ポリオレフィン系樹脂組成物 |
| JP2002173564A (ja) | 2000-12-06 | 2002-06-21 | Grand Polymer Co Ltd | 改質ポリプロピレン樹脂組成物、その製法、およびそれから得られる発泡体 |
| US6646056B2 (en) | 2001-10-16 | 2003-11-11 | Solvay Engineered Polymers | Thermoplastic elastomer compositions |
| JP4010141B2 (ja) | 2001-12-06 | 2007-11-21 | 住友化学株式会社 | 改質ポリプロピレン樹脂とその製造方法 |
| US20070004861A1 (en) | 2005-07-01 | 2007-01-04 | Kevin Cai | High melt strength polypropylene resins and method for making same |
| EP1892264A1 (en) | 2006-08-25 | 2008-02-27 | Borealis Technology Oy | Extrusion coated substrate |
| ES2331091T3 (es) | 2006-08-25 | 2009-12-21 | Borealis Technology Oy | Pelicula soplada de polipropileno. |
| DE502006007538D1 (de) | 2006-08-31 | 2010-09-09 | Treofan Germany Gmbh & Co Kg | Biaxial orientierte Elektroisolierfolie |
| ATE465859T1 (de) | 2007-01-31 | 2010-05-15 | Borealis Tech Oy | Einsatz eines langkettenverzweigten polypropylens zur verbreiterung des verarbeitungsfensters beim spritzstreckblasformen |
| EP2000504A1 (en) * | 2007-06-08 | 2008-12-10 | Borealis Technology Oy | Polymer composition with high impact resistance and high melt strength |
| EP2072546B2 (en) | 2007-12-18 | 2012-12-26 | Borealis Technology Oy | Heterophasic polypropylene with high impact properties |
| EP2113541A1 (en) * | 2008-04-28 | 2009-11-04 | Borealis AG | Adhesive propylene polymer composition suitable for extrusion coating of paper substrates |
| EP2338931A1 (en) | 2009-12-23 | 2011-06-29 | Borealis AG | Blown grade showing superior stiffness, transparency and processing behaviour |
| EP2386584A1 (en) * | 2010-05-11 | 2011-11-16 | Borealis AG | Polypropylene composition suitable for extrusion coating |
| EP2492293B1 (en) | 2011-02-28 | 2017-09-20 | Borealis AG | Polypropylene composition suitable for extrusion coating |
| EP2679630B1 (en) | 2012-06-28 | 2016-08-10 | Borealis AG | High melt strength polypropylene of improved quality |
| BR112015000935A2 (pt) | 2012-07-25 | 2017-06-27 | Borealis Ag | espuma produzida a partir de polipropileno com baixo conteúdo de gel |
-
2013
- 2013-07-19 CN CN201380037223.9A patent/CN104718249B/zh active Active
- 2013-07-19 JP JP2015523504A patent/JP5986314B2/ja active Active
- 2013-07-19 MX MX2015000615A patent/MX366376B/es active IP Right Grant
- 2013-07-19 WO PCT/EP2013/065263 patent/WO2014016206A1/en active Application Filing
- 2013-07-19 IN IN10848DEN2014 patent/IN2014DN10848A/en unknown
- 2013-07-19 BR BR112015000853A patent/BR112015000853A2/pt not_active Application Discontinuation
- 2013-07-19 US US14/414,825 patent/US9376549B2/en active Active
- 2013-07-19 CA CA2878305A patent/CA2878305C/en active Active
- 2013-07-19 EP EP13739223.9A patent/EP2877535B1/en active Active
- 2013-07-19 ES ES13739223.9T patent/ES2626363T3/es active Active
- 2013-07-19 KR KR1020157003771A patent/KR101531814B1/ko active Active
Also Published As
| Publication number | Publication date |
|---|---|
| CA2878305A1 (en) | 2014-01-30 |
| KR20150030767A (ko) | 2015-03-20 |
| JP5986314B2 (ja) | 2016-09-06 |
| BR112015000853A2 (pt) | 2017-06-27 |
| WO2014016206A1 (en) | 2014-01-30 |
| CN104718249A (zh) | 2015-06-17 |
| JP2015522701A (ja) | 2015-08-06 |
| MX2015000615A (es) | 2015-04-14 |
| EP2877535B1 (en) | 2017-03-15 |
| US20150133590A1 (en) | 2015-05-14 |
| KR101531814B1 (ko) | 2015-06-25 |
| EP2877535A1 (en) | 2015-06-03 |
| CN104718249B (zh) | 2017-03-29 |
| CA2878305C (en) | 2017-07-04 |
| US9376549B2 (en) | 2016-06-28 |
| MX366376B (es) | 2019-07-05 |
| IN2014DN10848A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2015-09-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2626363T3 (es) | Película con bajo índice de gel OCS | |
| ES2599456T3 (es) | Polipropileno de resistencia elevada a la fusión de calidad mejorada | |
| ES2634996T3 (es) | Espuma producida a partir de polipropileno con bajo contenido de gel | |
| ES2574437T3 (es) | Producción en una etapa de una composición de polipropileno |