AU732888B2 - Stabilizer combination for the rotomolding process - Google Patents
Stabilizer combination for the rotomolding process Download PDFInfo
- Publication number
- AU732888B2 AU732888B2 AU42792/97A AU4279297A AU732888B2 AU 732888 B2 AU732888 B2 AU 732888B2 AU 42792/97 A AU42792/97 A AU 42792/97A AU 4279297 A AU4279297 A AU 4279297A AU 732888 B2 AU732888 B2 AU 732888B2
- Authority
- AU
- Australia
- Prior art keywords
- alkyl
- hydrogen
- substituted
- oxygen
- unsubstituted
- 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.)
- Ceased
Links
- 238000000034 method Methods 0.000 title claims description 49
- 239000003381 stabilizer Substances 0.000 title claims description 25
- 238000001175 rotational moulding Methods 0.000 title claims description 15
- -1 2,4-di-tert-butylphenyl Chemical group 0.000 claims description 309
- 239000001257 hydrogen Substances 0.000 claims description 75
- 229910052739 hydrogen Inorganic materials 0.000 claims description 75
- 125000000217 alkyl group Chemical group 0.000 claims description 59
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 51
- 229910052760 oxygen Inorganic materials 0.000 claims description 51
- 239000001301 oxygen Substances 0.000 claims description 51
- 150000001875 compounds Chemical class 0.000 claims description 47
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 45
- 125000004432 carbon atom Chemical group C* 0.000 claims description 45
- 229910052717 sulfur Inorganic materials 0.000 claims description 45
- 239000011593 sulfur Substances 0.000 claims description 45
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 38
- 150000002431 hydrogen Chemical class 0.000 claims description 37
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 36
- 229920000098 polyolefin Polymers 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 31
- 125000003545 alkoxy group Chemical group 0.000 claims description 22
- 125000001589 carboacyl group Chemical group 0.000 claims description 20
- NPDLYUOYAGBHFB-WDSKDSINSA-N Asn-Arg Chemical compound NC(=O)C[C@H](N)C(=O)N[C@H](C(O)=O)CCCN=C(N)N NPDLYUOYAGBHFB-WDSKDSINSA-N 0.000 claims description 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 19
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
- 125000004423 acyloxy group Chemical group 0.000 claims description 14
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
- 125000004414 alkyl thio group Chemical group 0.000 claims description 12
- 125000002947 alkylene group Chemical group 0.000 claims description 12
- 125000001231 benzoyloxy group Chemical class C(C1=CC=CC=C1)(=O)O* 0.000 claims description 12
- 229910052751 metal Inorganic materials 0.000 claims description 12
- 239000002184 metal Substances 0.000 claims description 12
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 11
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 11
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 claims description 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 150000002367 halogens Chemical class 0.000 claims description 9
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 9
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims description 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 9
- 125000001544 thienyl group Chemical group 0.000 claims description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 7
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 7
- 125000005236 alkanoylamino group Chemical group 0.000 claims description 7
- 125000005605 benzo group Chemical group 0.000 claims description 7
- 239000000460 chlorine Substances 0.000 claims description 7
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 7
- 125000005561 phenanthryl group Chemical group 0.000 claims description 7
- 229920003023 plastic Polymers 0.000 claims description 7
- 239000004033 plastic Substances 0.000 claims description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 6
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 6
- 235000010290 biphenyl Nutrition 0.000 claims description 6
- 239000004305 biphenyl Substances 0.000 claims description 6
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 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
- 125000004987 dibenzofuryl group Chemical group C1(=CC=CC=2OC3=C(C21)C=CC=C3)* 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 125000005133 alkynyloxy group Chemical group 0.000 claims description 5
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 5
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 5
- 125000001624 naphthyl group Chemical group 0.000 claims description 5
- 125000004957 naphthylene group Chemical group 0.000 claims description 5
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 5
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 5
- 239000007983 Tris buffer Substances 0.000 claims description 4
- 125000004450 alkenylene group Chemical group 0.000 claims description 4
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- 125000004230 chromenyl group Chemical group O1C(C=CC2=CC=CC=C12)* 0.000 claims description 4
- 125000001041 indolyl group Chemical group 0.000 claims description 4
- 125000005956 isoquinolyl group Chemical group 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 claims description 4
- 125000001644 phenoxazinyl group Chemical group C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 claims description 4
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical group [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims description 4
- 125000004627 thianthrenyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3SC12)* 0.000 claims description 4
- 125000001834 xanthenyl group Chemical group C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 claims description 4
- 125000000641 acridinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 claims description 3
- 125000001118 alkylidene group Chemical group 0.000 claims description 3
- 150000001768 cations Chemical class 0.000 claims description 3
- 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 claims description 3
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 3
- FNIATMYXUPOJRW-UHFFFAOYSA-N cyclohexylidene Chemical group [C]1CCCCC1 FNIATMYXUPOJRW-UHFFFAOYSA-N 0.000 claims description 3
- 125000003838 furazanyl group Chemical group 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims description 3
- 125000001786 isothiazolyl group Chemical group 0.000 claims description 3
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 3
- 125000005327 perimidinyl group Chemical group N1C(=NC2=CC=CC3=CC=CC1=C23)* 0.000 claims description 3
- 125000004934 phenanthridinyl group Chemical group C1(=CC=CC2=NC=C3C=CC=CC3=C12)* 0.000 claims description 3
- 125000004625 phenanthrolinyl group Chemical group N1=C(C=CC2=CC=C3C=CC=NC3=C12)* 0.000 claims description 3
- 125000001791 phenazinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 claims description 3
- 125000000951 phenoxy group Chemical class [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 claims description 3
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 claims description 3
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 claims description 3
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 3
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 3
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 3
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims description 3
- 125000005493 quinolyl group Chemical group 0.000 claims description 3
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims description 3
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 claims description 3
- 238000011049 filling Methods 0.000 claims description 2
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims description 2
- 125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 0.000 claims description 2
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 125000004437 phosphorous atom Chemical group 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 238000003892 spreading Methods 0.000 claims description 2
- 101001053263 Homo sapiens Insulin gene enhancer protein ISL-1 Proteins 0.000 claims 3
- 102100024392 Insulin gene enhancer protein ISL-1 Human genes 0.000 claims 3
- 125000005201 cycloalkylcarbonyloxy group Chemical group 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 125000002098 pyridazinyl group Chemical group 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 description 49
- 229910052757 nitrogen Inorganic materials 0.000 description 23
- 229920001577 copolymer Polymers 0.000 description 20
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 17
- 239000000654 additive Substances 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 229920000642 polymer Polymers 0.000 description 11
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 10
- 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 10
- 150000001412 amines Chemical class 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 10
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 9
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 9
- 229920001684 low density polyethylene Polymers 0.000 description 9
- 239000004702 low-density polyethylene Substances 0.000 description 9
- 239000005977 Ethylene Substances 0.000 description 8
- 239000004743 Polypropylene Substances 0.000 description 8
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 8
- KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 8
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 8
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 8
- 239000004698 Polyethylene Substances 0.000 description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 125000004956 cyclohexylene group Chemical group 0.000 description 6
- 239000004700 high-density polyethylene Substances 0.000 description 6
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 6
- 229920000573 polyethylene Polymers 0.000 description 6
- 229920001155 polypropylene Polymers 0.000 description 6
- 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 5
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 5
- 239000012964 benzotriazole Substances 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 229920001903 high density polyethylene Polymers 0.000 description 5
- KXPXKNBDCUOENF-UHFFFAOYSA-N 2-(Octylthio)ethanol Chemical compound CCCCCCCCSCCO KXPXKNBDCUOENF-UHFFFAOYSA-N 0.000 description 4
- ZPIRWAHWDCHWLM-UHFFFAOYSA-N 2-dodecylsulfanylethanol Chemical compound CCCCCCCCCCCCSCCO ZPIRWAHWDCHWLM-UHFFFAOYSA-N 0.000 description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 150000001993 dienes Chemical class 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 150000005673 monoalkenes Chemical class 0.000 description 4
- UKJARPDLRWBRAX-UHFFFAOYSA-N n,n'-bis(2,2,6,6-tetramethylpiperidin-4-yl)hexane-1,6-diamine Chemical compound C1C(C)(C)NC(C)(C)CC1NCCCCCCNC1CC(C)(C)NC(C)(C)C1 UKJARPDLRWBRAX-UHFFFAOYSA-N 0.000 description 4
- FPQJEXTVQZHURJ-UHFFFAOYSA-N n,n'-bis(2-hydroxyethyl)oxamide Chemical compound OCCNC(=O)C(=O)NCCO FPQJEXTVQZHURJ-UHFFFAOYSA-N 0.000 description 4
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 4
- 150000002815 nickel Chemical class 0.000 description 4
- 239000001294 propane Substances 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 239000012744 reinforcing agent Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 4
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 4
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 3
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 3
- BPXVHIRIPLPOPT-UHFFFAOYSA-N 1,3,5-tris(2-hydroxyethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound OCCN1C(=O)N(CCO)C(=O)N(CCO)C1=O BPXVHIRIPLPOPT-UHFFFAOYSA-N 0.000 description 3
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 3
- ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical compound C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 description 3
- CKPKHTKLLYPGFM-UHFFFAOYSA-N 6,6-dimethylheptane-1,1-diol Chemical compound CC(CCCCC(O)O)(C)C CKPKHTKLLYPGFM-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 125000006639 cyclohexyl carbonyl group Chemical group 0.000 description 3
- 238000002845 discoloration Methods 0.000 description 3
- 239000003365 glass fiber Substances 0.000 description 3
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 3
- 239000003446 ligand Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 3
- 239000002530 phenolic antioxidant Substances 0.000 description 3
- 125000005954 phenoxathiinyl group Chemical group 0.000 description 3
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 3
- 229960004063 propylene glycol Drugs 0.000 description 3
- 235000013772 propylene glycol Nutrition 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 235000012222 talc Nutrition 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- 239000011732 tocopherol Substances 0.000 description 3
- 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 2
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 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
- ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 2
- MNCMBBIFTVWHIP-UHFFFAOYSA-N 1-anthracen-9-yl-2,2,2-trifluoroethanone Chemical group C1=CC=C2C(C(=O)C(F)(F)F)=C(C=CC=C3)C3=CC2=C1 MNCMBBIFTVWHIP-UHFFFAOYSA-N 0.000 description 2
- YEWBOZCFGXOUQW-UHFFFAOYSA-N 2,6,7-trioxa-1-phosphabicyclo[2.2.2]octan-4-ylmethanol Chemical compound C1OP2OCC1(CO)CO2 YEWBOZCFGXOUQW-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 2
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000000389 2-pyrrolyl group Chemical group [H]N1C([*])=C([H])C([H])=C1[H] 0.000 description 2
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- 239000004814 polyurethane Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 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
- 125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- TURAMGVWNUTQKH-UHFFFAOYSA-N propa-1,2-dien-1-one Chemical group C=C=C=O TURAMGVWNUTQKH-UHFFFAOYSA-N 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 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
- 238000000518 rheometry Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000010106 rotational casting Methods 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- IJRHDFLHUATAOS-DPMBMXLASA-M sodium ricinoleate Chemical compound [Na+].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O IJRHDFLHUATAOS-DPMBMXLASA-M 0.000 description 1
- 229940074404 sodium succinate Drugs 0.000 description 1
- ZDQYSKICYIVCPN-UHFFFAOYSA-L sodium succinate (anhydrous) Chemical compound [Na+].[Na+].[O-]C(=O)CCC([O-])=O ZDQYSKICYIVCPN-UHFFFAOYSA-L 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 125000003696 stearoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 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
- 125000006318 tert-butyl amino group Chemical group [H]N(*)C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- NZNAAUDJKMURFU-UHFFFAOYSA-N tetrakis(2,2,6,6-tetramethylpiperidin-4-yl) butane-1,2,3,4-tetracarboxylate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CC(C(=O)OC1CC(C)(C)NC(C)(C)C1)C(C(=O)OC1CC(C)(C)NC(C)(C)C1)CC(=O)OC1CC(C)(C)NC(C)(C)C1 NZNAAUDJKMURFU-UHFFFAOYSA-N 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 235000019149 tocopherols Nutrition 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
- 238000005809 transesterification reaction Methods 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 1
- 229920001862 ultra low molecular weight polyethylene Polymers 0.000 description 1
- 125000000297 undecanoyl group Chemical group O=C([*])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
- 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
- 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920001866 very low density polyethylene Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 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
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C41/00—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
- B29C41/003—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor characterised by the choice of material
-
- 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
- C08K5/1535—Five-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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/527—Cyclic esters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C41/00—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
- B29C41/02—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of definite length, i.e. discrete articles
- B29C41/04—Rotational or centrifugal casting, i.e. coating the inside of a mould by rotating the mould
- B29C41/06—Rotational or centrifugal casting, i.e. coating the inside of a mould by rotating the mould about two or more axes
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Moulding By Coating Moulds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH268096 | 1996-10-30 | ||
| CH2680/96 | 1996-10-30 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU4279297A AU4279297A (en) | 1998-05-07 |
| AU732888B2 true AU732888B2 (en) | 2001-05-03 |
Family
ID=4239168
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU42792/97A Ceased AU732888B2 (en) | 1996-10-30 | 1997-10-22 | Stabilizer combination for the rotomolding process |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US5883165A (enExample) |
| EP (1) | EP0839623B1 (enExample) |
| JP (1) | JPH10128773A (enExample) |
| AU (1) | AU732888B2 (enExample) |
| CA (1) | CA2219687C (enExample) |
| DE (1) | DE59702969D1 (enExample) |
Families Citing this family (158)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6521681B1 (en) * | 1996-07-05 | 2003-02-18 | Ciba Specialty Chemicals Corporation | Phenol-free stabilization of polyolefin fibres |
| AU8399398A (en) * | 1997-07-14 | 1999-02-10 | Dover Chemical Corporation | Lactone/phosphite blends |
| WO1999048997A1 (en) * | 1998-03-24 | 1999-09-30 | Ciba Specialty Chemicals Holding Inc. | Stabilisation of organic materials |
| US6770693B2 (en) | 1998-07-13 | 2004-08-03 | Dove Chemical Corporation | Blends of phosphites and antioxidants |
| US6214915B1 (en) * | 1998-12-10 | 2001-04-10 | General Electric Company | Stabilized thermoplastic compositions |
| US6444733B1 (en) * | 1999-03-01 | 2002-09-03 | Ciba Specialty Chemicals Corporation | Stabilizer combination for the rotomolding process |
| NL1014465C2 (nl) * | 1999-03-01 | 2002-01-29 | Ciba Sc Holding Ag | Stabilisatorcombinatie voor het rotomoldingproces. |
| DE19925125A1 (de) * | 1999-06-01 | 2000-12-07 | Bayer Ag | Polycarbonatformmassen zur Herstellung von Artikeln mit verminderter Staubanlagerung |
| DE10006208A1 (de) | 2000-02-11 | 2001-08-16 | Bayer Ag | IR-absorbierende Zusammensetzungen |
| GB0004043D0 (en) * | 2000-02-21 | 2000-04-12 | Borealis Polymers Oy | Polymer |
| AU722572B3 (en) * | 2000-03-01 | 2000-08-03 | Buckley, David Leonard | Golf club carrier |
| DE10022037A1 (de) * | 2000-05-05 | 2001-11-08 | Bayer Ag | IR-absorbierende Zusammensetzungen |
| EP1290106B1 (de) * | 2000-05-12 | 2009-08-12 | Bayer MaterialScience AG | Antistatikum |
| CN1282695C (zh) * | 2001-03-20 | 2006-11-01 | 西巴特殊化学品控股有限公司 | 阻燃剂组合物 |
| US20040048958A1 (en) * | 2002-09-06 | 2004-03-11 | Didier David A. | High temperature ultra high molecular weight polyethylene |
| US20040183053A1 (en) * | 2003-03-20 | 2004-09-23 | Pearson Jason Clay | Process for the preparation of a hindered amine light stabilizer salt |
| DE10360367A1 (de) * | 2003-12-22 | 2005-07-21 | Bayer Materialscience Ag | Stabilisierte thermoplastische Zusammensetzungen |
| US7611829B2 (en) | 2004-01-30 | 2009-11-03 | Fujifilm Corporation | Silver halide color photographic light-sensitive material and color image-forming method |
| US20080110377A1 (en) * | 2004-03-19 | 2008-05-15 | Henry Stevens | Load-Carrying Apparatus and Methods of Manufacture |
| CA2464551C (en) * | 2004-05-18 | 2012-01-03 | Nova Chemicals Corporation | Phenol free stabilization of polyethylene film |
| EP1600477A1 (en) * | 2004-05-28 | 2005-11-30 | Total Petrochemicals Research Feluy | Use of thermoplastic composition comprising polyethylene glycol as additive |
| EP1600474A1 (en) * | 2004-05-28 | 2005-11-30 | Total Petrochemicals Research Feluy | Use of fluoropolymers for rotomolding |
| US7390912B2 (en) * | 2004-12-17 | 2008-06-24 | Milliken & Company | Lactone stabilizing compositions |
| GB2425506B (en) * | 2005-04-26 | 2010-11-10 | Pvaxx Res & Dev Ltd | Load carrying apparatus and method of manufacture |
| US8399536B2 (en) | 2007-06-29 | 2013-03-19 | Basell Poliolefine Italia, s.r.l. | Irradiated polyolefin composition comprising a non-phenolic stabilizer |
| US8791189B2 (en) * | 2008-01-15 | 2014-07-29 | Sabic Innovative Plastics Ip B.V. | Moldable polyester compositions, processes of manufacture, and articles thereof |
| US8168707B2 (en) * | 2008-01-15 | 2012-05-01 | Sabic Innovative Plastics Ip B.V. | Moldable polyester compositions, processes of manufacture, and articles thereof |
| JP2010013659A (ja) * | 2009-09-11 | 2010-01-21 | Jsr Corp | 樹脂組成物および樹脂成形品 |
| DE102009058200A1 (de) | 2009-12-15 | 2011-06-16 | Bayer Materialscience Ag | Polymer-Zusammensetzung mit Wärme-absorbierenden Eigenschaften und hoher Stabilität |
| DE102009058462A1 (de) | 2009-12-16 | 2011-06-22 | Bayer MaterialScience AG, 51373 | Polycarbonat mit erhöhter Transmission und bakterizider Wirksamkeit |
| ITRM20100228A1 (it) | 2010-05-10 | 2011-11-10 | Bayer Materialscience Ag | Composizione polimerica con caratteristiche di assorbimento del calore e migliorate caratteristiche di colore. |
| ITRM20100225A1 (it) | 2010-05-10 | 2011-11-10 | Bayer Materialscience Ag | Composizione di polimeri con caratteristiche di assorbimento del calore e migliorate caratteristiche di colore. |
| ITRM20100227A1 (it) | 2010-05-10 | 2011-11-10 | Bayer Materialscience Ag | Composizione polimerica con caratteristiche di assorbimento di calore ad alta stabilità. |
| ITRM20100226A1 (it) | 2010-05-10 | 2011-11-10 | Bayer Materialscience Ag | Composizioni stabilizzanti. |
| ES2498928T3 (es) | 2010-10-25 | 2014-09-26 | Bayer Intellectual Property Gmbh | Estructura multicapa de plástico con baja transmisión de energía |
| DE102010042939A1 (de) | 2010-10-26 | 2012-04-26 | Bayer Materialscience Aktiengesellschaft | Fugenlose Heckklappe |
| EP3786216A1 (en) | 2010-12-13 | 2021-03-03 | Cytec Technology Corp. | Processing additives and uses of same in rotational molding |
| US11267951B2 (en) | 2010-12-13 | 2022-03-08 | Cytec Technology Corp. | Stabilizer compositions containing substituted chroman compounds and methods of use |
| IT1403380B1 (it) | 2010-12-17 | 2013-10-17 | Bayer Materialscience Ag | Composizione di polimeri con caratteristiche di assorbimento di calore ad alta stabilità agli agenti atmosferici. |
| ITRM20100670A1 (it) | 2010-12-17 | 2012-06-18 | Bayer Materialscience Ag | Colorante organico e composizioni polimeriche colorate ad alta stabilità agli agenti atmosferici. |
| ITRM20100668A1 (it) | 2010-12-17 | 2012-06-18 | Bayer Materialscience Ag | Substrato-led a colorazione stabile. |
| ITRM20100667A1 (it) | 2010-12-17 | 2012-06-18 | Bayer Materialscience Ag | Composizione di polimeri con caratteristiche di assorbimento di calore ad alta stabilità agli agenti atmosferici. |
| EP2468820A1 (en) | 2010-12-23 | 2012-06-27 | Bayer MaterialScience AG | Polycarbonate compositions with improved flame resistance |
| MX360808B (es) * | 2011-05-02 | 2018-11-16 | Basf Se | Derivados de 5h - furan - 2 - ona para la estabilización de material orgánico. |
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| AU2012324995C1 (en) | 2011-10-18 | 2016-12-15 | Covestro Deutschland Ag | Polymer composition with heat-absorbing properties |
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| WO2013079599A1 (de) | 2011-11-30 | 2013-06-06 | Bayer Intellectual Property Gmbh | Polycarbonatzusammensetzungen mit verbesserter oberfläche |
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| JP6605456B2 (ja) | 2013-10-08 | 2019-11-13 | コベストロ、ドイチュラント、アクチエンゲゼルシャフト | ポリシロキサン−ポリカーボネートブロック共縮合物 |
| ES2655496T3 (es) | 2014-01-30 | 2018-02-20 | Covestro Deutschland Ag | Co-condensados de bloque de polisiloxano-policarbonato con propiedades reológicas mejoradas |
| EP2955201A1 (de) | 2014-06-11 | 2015-12-16 | Covestro Deutschland AG | Glasfaserverstärkte Polycarbonat-Zusammensetzungen |
| KR102377818B1 (ko) * | 2014-08-05 | 2022-03-24 | 바스프 에스이 | 안정화제로서의 3-페닐-벤조푸란-2-온 디포스파이트 유도체 |
| KR102391932B1 (ko) | 2014-09-11 | 2022-04-28 | 코베스트로 도이칠란트 아게 | 자동차 글레이징 시스템용 트림 |
| JP6804446B2 (ja) | 2014-12-01 | 2020-12-23 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトＣｏｖｅｓｔｒｏ Ｄｅｕｔｓｃｈｌａｎｄ Ａｇ | 改善した流動性および高剛性を有する充填ポリカーボネート組成物 |
| US10119009B2 (en) | 2014-12-01 | 2018-11-06 | Covestro Deutschland Ag | Flowability of polycarbonate compositions |
| TWI687485B (zh) | 2015-01-20 | 2020-03-11 | 德商科思創德意志股份有限公司 | 包含玻璃纖維與含矽氧烷之聚碳酸酯嵌段共聚物的阻燃模塑組成物 |
| WO2016116395A1 (de) | 2015-01-20 | 2016-07-28 | Covestro Deutschland Ag | Flammgeschützte formmassen enthaltend siloxan-haltiges polycarbonat-blockcokondensat |
| JP2018510953A (ja) | 2015-04-07 | 2018-04-19 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトＣｏｖｅｓｔｒｏ Ｄｅｕｔｓｃｈｌａｎｄ Ａｇ | ポリシロキサンおよびジヒドロキシジフェニルシクロアルカン（コ）ポリカーボネートのブロック共縮合物 |
| ES2667345T3 (es) | 2015-07-08 | 2018-05-10 | Covestro Deutschland Ag | Mejora de la capacidad de flujo de composiciones de policarbonato térmicamente conductoras |
| EP3115417A1 (de) | 2015-07-08 | 2017-01-11 | Covestro Deutschland AG | Schlagzähmodifizierte polycarbonatzusammensetzungen mit verbesserter fliessfähigkeit und hoher wärmeformbeständigkeit |
| EP3115405B1 (de) | 2015-07-08 | 2017-12-27 | Covestro Deutschland AG | Bornitrid-haltige thermoplastische zusammensetzung |
| EP3115404B1 (de) | 2015-07-08 | 2018-01-31 | Covestro Deutschland AG | Bornitrid-hybridmaterial-haltige thermoplastische zusammensetzung |
| EP3368296B1 (de) | 2015-10-26 | 2020-08-19 | Covestro Deutschland AG | Mehrschichtiger faserverbundwerkstoff |
| CN108136717A (zh) | 2015-10-26 | 2018-06-08 | 科思创德国股份有限公司 | 多层纤维复合材料 |
| CA2913280C (en) | 2015-11-25 | 2022-07-26 | Nova Chemicals Corporation | Phenol free stabilization of polyethylene |
| US10669418B2 (en) | 2015-12-11 | 2020-06-02 | Covestro Deutschland Ag | Polycarbonate compositions containing polyglycidyl ether |
| JP2019500244A (ja) | 2015-12-17 | 2019-01-10 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトＣｏｖｅｓｔｒｏ Ｄｅｕｔｓｃｈｌａｎｄ Ａｇ | 半製品ウェブを製造する機器および方法 |
| US10676613B2 (en) | 2016-04-14 | 2020-06-09 | Covestro Deutschland Ag | Poycarbonate compositions containing isosorbide diesters |
| KR102351908B1 (ko) | 2016-05-04 | 2022-01-18 | 코베스트로 도이칠란트 아게 | 3-d 프린팅에서의 지지 물질로서의 코폴리카르보네이트 |
| TW201809099A (zh) | 2016-05-19 | 2018-03-16 | 科思創德意志股份有限公司 | 含有羧酸及其甘油或二甘油酯之聚碳酸酯組成物 |
| JP6972026B2 (ja) | 2016-05-24 | 2021-11-24 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトCovestro Deutschland Ag | 充填剤、カルボン酸およびそのグリセロールまたはジグリセロールエステルを含んでなるポリカーボネート組成物 |
| US11130321B2 (en) | 2016-06-03 | 2021-09-28 | Covestro Deutschland Ag | Multi-layer composite material containing special copolycarbonates as a matrix material |
| KR20190042578A (ko) | 2016-08-24 | 2019-04-24 | 코베스트로 도이칠란트 아게 | 활석을 포함하는 폴리카르보네이트 조성물 |
| EP3519217B1 (de) | 2016-09-27 | 2021-06-30 | Covestro Intellectual Property GmbH & Co. KG | Kraftfahrzeug, aufweisend zwei a-säulen und eine frontscheibe |
| US11273419B2 (en) | 2016-10-05 | 2022-03-15 | Covestro Deutschland Ag | Mixing elements with a reduced structural depth for static mixers |
| EP3541624B1 (de) | 2016-11-17 | 2020-09-09 | Covestro Deutschland AG | Opaker mehrschichtkörper aus polycarbonat zum wärmemanagement |
| WO2018091556A1 (de) | 2016-11-17 | 2018-05-24 | Covestro Deutschland Ag | Transparenter mehrschichtkörper zum wärmemanagement |
| EP3555179B1 (en) | 2016-12-19 | 2021-07-07 | Covestro Intellectual Property GmbH & Co. KG | Production of siloxane-containing block copolycarbonates by means of compatibilizers |
| CA2953610A1 (en) | 2017-01-05 | 2018-07-05 | Nova Chemicals Corporation | Mixed phosphite stabilization of polyethylene film |
| CN110177831B (zh) | 2017-01-23 | 2022-04-29 | 科思创德国股份有限公司 | 含有流动助剂的含石墨的聚碳酸酯组合物 |
| EP3354433A1 (de) | 2017-01-31 | 2018-08-01 | Covestro Deutschland AG | Vorrichtung mit freilaufenden kühlwalzen zur herstellung eines faserverbundwerkstoffs in form eines mit polymer imprägnierten faserbands, verfahren zur herstellung dieses faserbands, ein imprägniertes faserband und ein aus dem imprägnierten faserband hergestellter mehrschichtverbund |
| US11472099B2 (en) | 2017-02-14 | 2022-10-18 | Covestro Deutschland Ag | Method for producing an object by means of an additive manufacturing process using a polycarbonate building material with improved flowability |
| EP3381636A1 (de) | 2017-03-28 | 2018-10-03 | Covestro Deutschland AG | Benetzungsdüse mit benetzungstaschen zur herstellung eines mit polymer benetzten faserbands, verfahren zur herstellung dieses faserbands und ein benetztes faserband |
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| EP3395898B1 (de) | 2017-04-28 | 2020-02-05 | Covestro Deutschland AG | Polycarbonatzusammensetzung mit perlglanzpigment und/oder interferenzpigment |
| EP3658613A1 (de) | 2017-07-24 | 2020-06-03 | Covestro Deutschland AG | Led-beleuchtungselemente mit formteilen aus transluzenten polycarbonat-zusammensetzungen mit tiefenglanzeffekt |
| EP3502306B1 (de) | 2017-12-19 | 2022-03-02 | Covestro Deutschland AG | Mehrschichtkörper, umfassend eine substratschicht enthaltend polycarbonat, talk und wachs |
| EP3502183B1 (de) | 2017-12-20 | 2020-10-21 | Covestro Deutschland AG | Talk-gefüllte polycarbonat-zusammensetzungen |
| EP3502182B1 (de) | 2017-12-20 | 2020-10-21 | Covestro Deutschland AG | Stabilisierte, gefüllte polycarbonat-zusammensetzungen |
| KR102744687B1 (ko) | 2017-12-21 | 2024-12-23 | 코베스트로 도이칠란트 아게 | 다층체 및 LiDAR 센서를 포함하는 장치 |
| US12024628B2 (en) | 2018-04-16 | 2024-07-02 | Covestro Intellectual Property Gmbh & Co. Kg | By means of ionizing radiation sterilizable moulded parts made from polycarbonate |
| EP3781630B1 (en) | 2018-04-16 | 2022-10-12 | Covestro Intellectual Property GmbH & Co. KG | By means of ionizing radiation sterilizable moulded parts made from polycarbonate |
| EP3564577A1 (de) | 2018-05-03 | 2019-11-06 | Katholieke Universiteit Leuven K.U. Leuven R&D | Optische lichtleitplatte |
| WO2019219615A1 (de) | 2018-05-17 | 2019-11-21 | Covestro Deutschland Ag | Gefüllte polycarbonat-zusammensetzungen mit guter kratzfestigkeit und reduzierter vergilbung |
| EP3572469A1 (de) | 2018-05-25 | 2019-11-27 | Covestro Deutschland AG | Polycarbonatzusammensetzung mit perlglanzpigment und/oder interferenzpigment |
| EP3575362A1 (de) | 2018-05-29 | 2019-12-04 | Covestro Deutschland AG | Abdeckungen für led-lichtquellen |
| JP2021531995A (ja) | 2018-05-29 | 2021-11-25 | コベストロ・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング・アンド・コー・カーゲー | 高い耐候安定性を有する、ポリカーボネート製の不透明多層体 |
| EP3581605A1 (de) | 2018-06-14 | 2019-12-18 | Covestro Deutschland AG | Schmelzeumesterungsverfahren zur gleichzeitigen herstellung mindestens zweier verschiedenartiger polycarbonate in einer produktionsanlage |
| MX2020007184A (es) † | 2018-07-12 | 2020-09-09 | Lg Chemical Ltd | Composicion plastificante que comprende una sustancia a base de ciclohexano poliester y composicion de resina que la comprende. |
| EP3841166B2 (en) | 2018-08-22 | 2025-05-07 | Basf Se | Stabilized rotomolded polyolefin |
| WO2020083800A1 (de) | 2018-10-26 | 2020-04-30 | Covestro Deutschland Ag | Additives fertigungsverfahren mit einem aufbaumaterial enthaltend metalloxid-beschichteten glimmer |
| ES2933516T3 (es) | 2019-04-02 | 2023-02-09 | Covestro Deutschland Ag | Co-policarbonatos en bloque que contienen siloxano con un tamaño de dominio pequeño |
| EP4010401A1 (en) | 2019-08-08 | 2022-06-15 | Covestro Intellectual Property GmbH & Co. KG | Process for the preparation of a polycarbonate |
| DE202020101944U1 (de) | 2019-09-30 | 2021-01-15 | Covestro Deutschland Ag | LED-Beleuchtungselemente auf Basis von Mehrschichtkörpern mit Steinoptik |
| DE202020101945U1 (de) | 2019-09-30 | 2021-01-15 | Covestro Deutschland Ag | LED-Beleuchtungselemente auf Basis von Mehrschichtkörpern mit Massivsteinoptik |
| EP3804938A1 (de) | 2019-10-07 | 2021-04-14 | Covestro Deutschland AG | Fahrzeugsitz enthaltend faserverbundwerkstoff und expandierte thermoplastische kunststoffe |
| EP3808544A1 (de) | 2019-10-14 | 2021-04-21 | Covestro Deutschland AG | Direkt-imprägnierungs prozess |
| EP3815898A1 (de) | 2019-10-28 | 2021-05-05 | Covestro Deutschland AG | Schichtenverbund aus polycarbonat und polycarbonatblend zur verbesserten lackierbarkeit |
| EP3838979B1 (de) | 2019-12-17 | 2024-06-26 | Covestro Deutschland AG | Schmelzepolycarbonat mit verbesserten optischen eigenschaften |
| EP3916055A1 (de) | 2020-05-26 | 2021-12-01 | Covestro Deutschland AG | Polycarbonat-zusammensetzungen enthaltend polyethercarbonatpolyole |
| DE202020005721U1 (de) | 2020-06-08 | 2022-03-08 | Lanxess Deutschland Gmbh | Mehrschichtverbundwerkstoff |
| EP3922452A1 (de) | 2020-06-08 | 2021-12-15 | LANXESS Deutschland GmbH | Mehrschichtverbundwerkstoff |
| EP3985047A1 (de) | 2020-10-13 | 2022-04-20 | Covestro Deutschland AG | Verfahren zur herstellung eines polycarbonats nach dem phasengrenzflächenverfahren unter lösungsmittelaustausch |
| US20230407044A1 (en) | 2020-11-23 | 2023-12-21 | Covestro Deutschland Ag | Polycarbonate Compositions Containing Titanium Dioxide and Metal Oxide-Coated Mica Particles |
| EP4247888A1 (de) | 2020-11-23 | 2023-09-27 | Covestro Deutschland AG | Verbesserung der reflexion und des yellowness-index bei thermoplastischen reflective white-zusammensetzungen |
| CN116457405A (zh) | 2020-11-23 | 2023-07-18 | 科思创德国股份有限公司 | 阻燃的含二氧化钛的聚碳酸酯组合物 |
| EP4247886A1 (de) | 2020-11-23 | 2023-09-27 | Covestro Deutschland AG | Polycarbonat-zusammensetzungen enthaltend titandioxid und epoxy-gruppen enthaltendes triacylglycerol |
| US12313866B2 (en) | 2020-11-30 | 2025-05-27 | Covestro Deutschland Ag | Multi-layer structure suitable for use as a reflector |
| EP4251688B1 (de) | 2020-11-30 | 2024-09-25 | Covestro Deutschland AG | Polycarbonat-zusammensetzungen enthaltend titandioxid und eine titandioxid-beschichtung umfassende glas-plättchen |
| EP4083136A1 (de) | 2021-04-30 | 2022-11-02 | Covestro Deutschland AG | Polycarbonat-zusammensetzungen mit zinksulfid als weisspigment |
| EP4092070A1 (de) | 2021-05-17 | 2022-11-23 | Covestro Deutschland AG | Reduzierung des gehalts spezieller salze von sulfonsäure-, sulfonamiden- oder sulfonimidderivaten im abwasser |
| EP4092075A1 (de) | 2021-05-17 | 2022-11-23 | Covestro Deutschland AG | Flammwidrige zusammensetzung umfassend 0,040 bis 0,095 gew.-% eines flammschutzmittels |
| EP4098690A1 (de) | 2021-06-01 | 2022-12-07 | Covestro Deutschland AG | Thermoplastische zusammensetzung mit hoher wärmeformbeständigkeit und reflexion |
| CN117500859A (zh) | 2021-06-15 | 2024-02-02 | 科思创德国股份有限公司 | 包含间苯二酚和间苯二甲酸和/或对苯二甲酸的低聚酯、相应的聚酯碳酸酯及其制备 |
| EP4355827A1 (de) | 2021-06-18 | 2024-04-24 | Covestro Deutschland AG | Flammgeschützte polycarbonat-zusammensetzungen mit hohem cti |
| WO2023012085A1 (de) | 2021-08-04 | 2023-02-09 | Covestro Deutschland Ag | Polycarbonat-zusammensetzungen mit hohem cti |
| EP4194479A1 (de) | 2021-12-07 | 2023-06-14 | Covestro Deutschland AG | Gute schlagzähigkeit bei mechanisch recyceltem polycarbonat |
| EP4194478A1 (de) | 2021-12-07 | 2023-06-14 | Covestro Deutschland AG | Verbesserte hydrolysestabilität bei polycarbonat-zusammensetzungen |
| KR20240164521A (ko) | 2022-03-25 | 2024-11-19 | 코베스트로 도이칠란트 아게 | 높은 cti를 갖는 폴리카르보네이트 조성물 |
| KR20240168324A (ko) | 2022-03-25 | 2024-11-29 | 코베스트로 도이칠란트 아게 | 높은 cti를 갖는 복합 폴리카르보네이트 요소를 포함하는 ee 부품 |
| JP2025510107A (ja) | 2022-03-25 | 2025-04-14 | コベストロ、ドイチュラント、アクチエンゲゼルシャフト | 高ｃｔｉを有するポリカーボネート組成物 |
| JP2025512094A (ja) | 2022-04-14 | 2025-04-16 | コベストロ、ドイチュラント、アクチエンゲゼルシャフト | 高い比較トラッキング指数を有する熱伝導性防炎性ポリカーボネート組成物 |
| CN119032135A (zh) | 2022-04-14 | 2024-11-26 | 科思创德国股份有限公司 | 具有高相比漏电起痕指数的阻燃导热聚碳酸酯组合物 |
| EP4286452A1 (en) | 2022-05-30 | 2023-12-06 | Covestro LLC | Polycarbonate diagnostic components with reduced fluorescence |
| CN120418753A (zh) | 2022-10-28 | 2025-08-01 | 科思创有限公司 | 用于人机接口（hmi）的蛤壳式外壳 |
| CN120569691A (zh) | 2022-10-28 | 2025-08-29 | 科思创有限公司 | 可再循环塑料组装件 |
| WO2024091777A1 (en) | 2022-10-28 | 2024-05-02 | Covestro Llc | Consolidated human-machine interface (hmi) chassis |
| EP4378492A1 (de) | 2022-12-01 | 2024-06-05 | Covestro Deutschland AG | Medizinprodukt mit hoher intralipidbeständigkeit aus polycarbonatmaterial |
| DE102023000052A1 (de) | 2023-01-12 | 2024-07-18 | Covestro Deutschland Ag | Herstellung eines zumindest teilweise beschichteten Formkörpers ohne Reinraum unter Verwendung einer PC-Zusammensetzung mit verbesserten Antistatikeigenschaften |
| EP4450545A1 (de) | 2023-04-19 | 2024-10-23 | Covestro Deutschland AG | Verfahren zur herstellung von nachexpandierbaren polycarbonat-beads und entsprechende polycarbonat-beads |
| EP4450544B1 (de) | 2023-04-19 | 2025-12-10 | Covestro Deutschland AG | Verfahren zur herstellung von polycarbonat-beads |
| EP4552819A1 (en) | 2023-11-10 | 2025-05-14 | Covestro LLC | Plate metal insert molding with polycarbonate and polycarbonate blends |
| EP4600008A1 (en) | 2024-02-08 | 2025-08-13 | Covestro LLC | Sacrificial section for more sustainable plastic parts |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2042562B (en) * | 1979-02-05 | 1983-05-11 | Sandoz Ltd | Stabilising polymers |
| US4388244A (en) | 1981-06-09 | 1983-06-14 | Ashland Oil, Inc. | Petrolatum or hydrocarbon wax oxidate composition |
| CA1230271A (en) * | 1983-12-12 | 1987-12-15 | Ahmed A. Alim | Rotational molding grade lldpe resin |
| EP0415887B1 (de) * | 1989-08-31 | 1994-10-05 | Ciba-Geigy Ag | 3-Phenylbenzofuran-2-one |
| US5175312A (en) | 1989-08-31 | 1992-12-29 | Ciba-Geigy Corporation | 3-phenylbenzofuran-2-ones |
| GB2252325A (en) * | 1991-01-31 | 1992-08-05 | Ciba Geigy Ag | Stabilised polyolefin |
| TW206220B (enExample) | 1991-07-01 | 1993-05-21 | Ciba Geigy Ag | |
| US5252643A (en) | 1991-07-01 | 1993-10-12 | Ciba-Geigy Corporation | Thiomethylated benzofuran-2-ones |
| TW260686B (enExample) | 1992-05-22 | 1995-10-21 | Ciba Geigy | |
| NL9300801A (nl) | 1992-05-22 | 1993-12-16 | Ciba Geigy | 3-(acyloxyfenyl)benzofuran-2-on als stabilisatoren. |
| GB2267490B (en) | 1992-05-22 | 1995-08-09 | Ciba Geigy Ag | 3-(Carboxymethoxyphenyl)benzofuran-2-one stabilisers |
| MX9305489A (es) * | 1992-09-23 | 1994-03-31 | Ciba Geigy Ag | 3-(dihidrobenzofuran-5-il)benzofuran-2-onas, estabilizadores. |
| TW255902B (enExample) | 1992-09-23 | 1995-09-01 | Ciba Geigy | |
| DE4237637A1 (de) * | 1992-11-07 | 1994-05-11 | Basf Ag | Verfahren zur Herstellung von Polypropylenhäuten |
| TW270133B (enExample) * | 1993-09-17 | 1996-02-11 | Ciba Geigy | |
| CH686306A5 (de) | 1993-09-17 | 1996-02-29 | Ciba Geigy Ag | 3-Aryl-benzofuranone als Stabilisatoren. |
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- 1997-10-21 DE DE59702969T patent/DE59702969D1/de not_active Expired - Fee Related
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- 1997-10-27 US US08/958,679 patent/US5883165A/en not_active Expired - Lifetime
- 1997-10-28 CA CA002219687A patent/CA2219687C/en not_active Expired - Fee Related
- 1997-10-29 JP JP9312630A patent/JPH10128773A/ja not_active Ceased
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| AU4279297A (en) | 1998-05-07 |
| US5883165A (en) | 1999-03-16 |
| EP0839623B1 (de) | 2001-01-31 |
| EP0839623A1 (de) | 1998-05-06 |
| CA2219687C (en) | 2005-06-14 |
| CA2219687A1 (en) | 1998-04-30 |
| JPH10128773A (ja) | 1998-05-19 |
| DE59702969D1 (de) | 2001-03-08 |
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