ZA200405251B - Prestabilization of hologen-containing polymers. - Google Patents

Prestabilization of hologen-containing polymers. Download PDF

Info

Publication number: ZA200405251B
Authority: ZA; South Africa
Prior art keywords: polymer; process according; pvc; weight; hydroxy
Prior art date: 2001-12-04

Application number

ZA200405251A

Other languages

English (en)

Inventor

Karl-Josef Kuhn

Hans-Helmut Friedrich

Original Assignee

Crompton Vinyl Additives Gmbh

Priority date (The priority date 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 date listed.)

2001-12-04

Filing date

2004-07-01

Publication date

2005-06-21

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=7707879&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ZA200405251(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2004-07-01 Application filed by Crompton Vinyl Additives Gmbh filed Critical Crompton Vinyl Additives Gmbh

2005-06-21 Publication of ZA200405251B publication Critical patent/ZA200405251B/en

Links

229920000642 polymer Polymers 0.000 title claims description 66
239000000203 mixture Substances 0.000 claims description 61
238000006116 polymerization reaction Methods 0.000 claims description 49
239000003381 stabilizer Substances 0.000 claims description 49
-1 dicyclohexylmethanylene Chemical group 0.000 claims description 40
238000000034 method Methods 0.000 claims description 35
150000001875 compounds Chemical class 0.000 claims description 31
239000000654 additive Substances 0.000 claims description 21
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 19
229910052736 halogen Inorganic materials 0.000 claims description 18
150000002367 halogens Chemical class 0.000 claims description 18
239000000725 suspension Substances 0.000 claims description 13
239000000178 monomer Substances 0.000 claims description 12
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 9
150000001412 amines Chemical class 0.000 claims description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
150000003839 salts Chemical class 0.000 claims description 9
239000011734 sodium Substances 0.000 claims description 9
229910052725 zinc Inorganic materials 0.000 claims description 9
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical group NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 8
229910052739 hydrogen Inorganic materials 0.000 claims description 8
238000004519 manufacturing process Methods 0.000 claims description 8
229910052791 calcium Inorganic materials 0.000 claims description 7
229910052749 magnesium Inorganic materials 0.000 claims description 7
229910052799 carbon Inorganic materials 0.000 claims description 6
LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 claims description 6
229940043276 diisopropanolamine Drugs 0.000 claims description 6
229910052712 strontium Inorganic materials 0.000 claims description 6
SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 claims description 5
239000007983 Tris buffer Substances 0.000 claims description 5
229910052788 barium Inorganic materials 0.000 claims description 5
229910052700 potassium Inorganic materials 0.000 claims description 5
229910052782 aluminium Inorganic materials 0.000 claims description 4
229910021529 ammonia Inorganic materials 0.000 claims description 4
239000007795 chemical reaction product Substances 0.000 claims description 4
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 4
229910052744 lithium Inorganic materials 0.000 claims description 4
VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 4
229910052708 sodium Inorganic materials 0.000 claims description 4
238000006467 substitution reaction Methods 0.000 claims description 4
101100097467 Arabidopsis thaliana SYD gene Proteins 0.000 claims description 3
229910052684 Cerium Inorganic materials 0.000 claims description 3
239000004908 Emulsion polymer Substances 0.000 claims description 3
101100495925 Schizosaccharomyces pombe (strain 972 / ATCC 24843) chr3 gene Proteins 0.000 claims description 3
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical group OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 3
238000002955 isolation Methods 0.000 claims description 3
229910052746 lanthanum Inorganic materials 0.000 claims description 3
229910001488 sodium perchlorate Inorganic materials 0.000 claims description 3
COMSLVZXDHSHPO-UHFFFAOYSA-N 1-[bis(2-hydroxyethyl)amino]-3-decoxypropan-2-ol Chemical compound CCCCCCCCCCOCC(O)CN(CCO)CCO COMSLVZXDHSHPO-UHFFFAOYSA-N 0.000 claims description 2
GGHQVHKMWVITSI-UHFFFAOYSA-N 1-[bis(2-hydroxyethyl)amino]hexadecan-2-ol Chemical compound CCCCCCCCCCCCCCC(O)CN(CCO)CCO GGHQVHKMWVITSI-UHFFFAOYSA-N 0.000 claims description 2
ZFECCYLNALETDE-UHFFFAOYSA-N 1-[bis(2-hydroxyethyl)amino]propan-2-ol Chemical compound CC(O)CN(CCO)CCO ZFECCYLNALETDE-UHFFFAOYSA-N 0.000 claims description 2
OECTYKWYRCHAKR-UHFFFAOYSA-N 4-vinylcyclohexene dioxide Chemical compound C1OC1C1CC2OC2CC1 OECTYKWYRCHAKR-UHFFFAOYSA-N 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
125000005265 dialkylamine group Chemical group 0.000 claims description 2
125000005842 heteroatom Chemical group 0.000 claims description 2
229910052760 oxygen Inorganic materials 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
BAZAXWOYCMUHIX-UHFFFAOYSA-M sodium perchlorate Chemical compound [Na+].[O-]Cl(=O)(=O)=O BAZAXWOYCMUHIX-UHFFFAOYSA-M 0.000 claims description 2
239000003017 thermal stabilizer Substances 0.000 claims 5
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims 4
150000002924 oxiranes Chemical class 0.000 claims 2
HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 claims 1
229910013711 M(ClO4)n Inorganic materials 0.000 claims 1
125000005741 alkyl alkenyl group Chemical group 0.000 claims 1
BQQUFAMSJAKLNB-UHFFFAOYSA-N dicyclopentadiene diepoxide Chemical group C12C(C3OC33)CC3C2CC2C1O2 BQQUFAMSJAKLNB-UHFFFAOYSA-N 0.000 claims 1
POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 claims 1
229910052717 sulfur Inorganic materials 0.000 claims 1
239000004800 polyvinyl chloride Substances 0.000 description 65
229920000915 polyvinyl chloride Polymers 0.000 description 65
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 39
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 37
239000000843 powder Substances 0.000 description 21
239000002609 medium Substances 0.000 description 20
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 16
229920001577 copolymer Polymers 0.000 description 15
150000002148 esters Chemical class 0.000 description 14
238000011105 stabilization Methods 0.000 description 14
238000012360 testing method Methods 0.000 description 13
238000007792 addition Methods 0.000 description 11
239000011575 calcium Substances 0.000 description 11
239000004014 plasticizer Substances 0.000 description 11
239000011701 zinc Substances 0.000 description 11
239000004305 biphenyl Substances 0.000 description 10
235000010290 biphenyl Nutrition 0.000 description 10
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 10
239000000049 pigment Substances 0.000 description 10
229920003023 plastic Polymers 0.000 description 10
239000004033 plastic Substances 0.000 description 10
230000006641 stabilisation Effects 0.000 description 10
239000010457 zeolite Substances 0.000 description 10
229910052751 metal Inorganic materials 0.000 description 9
239000002184 metal Substances 0.000 description 9
239000000243 solution Substances 0.000 description 9
XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 8
239000006185 dispersion Substances 0.000 description 8
238000009472 formulation Methods 0.000 description 8
239000003999 initiator Substances 0.000 description 8
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 7
239000004676 acrylonitrile butadiene styrene Substances 0.000 description 7
239000000839 emulsion Substances 0.000 description 7
239000011777 magnesium Substances 0.000 description 7
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 7
239000000344 soap Substances 0.000 description 7
239000007787 solid Substances 0.000 description 7
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 6
125000004429 atom Chemical group 0.000 description 6
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
238000007033 dehydrochlorination reaction Methods 0.000 description 6
239000005038 ethylene vinyl acetate Substances 0.000 description 6
239000000314 lubricant Substances 0.000 description 6
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 6
229920005862 polyol Polymers 0.000 description 6
150000003077 polyols Chemical class 0.000 description 6
BIHLHMHULOMJLI-UHFFFAOYSA-N 3-[bis(2-hydroxyethyl)amino]propan-1-ol Chemical compound OCCCN(CCO)CCO BIHLHMHULOMJLI-UHFFFAOYSA-N 0.000 description 5
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 5
239000004593 Epoxy Chemical class 0.000 description 5
229910021536 Zeolite Inorganic materials 0.000 description 5
229910052783 alkali metal Inorganic materials 0.000 description 5
229910052784 alkaline earth metal Inorganic materials 0.000 description 5
239000003795 chemical substances by application Substances 0.000 description 5
235000014113 dietary fatty acids Nutrition 0.000 description 5
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 5
238000001035 drying Methods 0.000 description 5
239000000194 fatty acid Substances 0.000 description 5
229930195729 fatty acid Natural products 0.000 description 5
239000000945 filler Substances 0.000 description 5
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 5
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 5
239000000463 material Substances 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
229920002959 polymer blend Polymers 0.000 description 5
239000000047 product Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
229920002554 vinyl polymer Polymers 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
229920000459 Nitrile rubber Polymers 0.000 description 4
BDJRBEYXGGNYIS-UHFFFAOYSA-N Nonanedioid acid Natural products OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 4
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 4
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
150000001340 alkali metals Chemical class 0.000 description 4
150000001342 alkaline earth metals Chemical class 0.000 description 4
239000003963 antioxidant agent Substances 0.000 description 4
235000006708 antioxidants Nutrition 0.000 description 4
125000006267 biphenyl group Chemical group 0.000 description 4
230000015556 catabolic process Effects 0.000 description 4
230000000694 effects Effects 0.000 description 4
229920001519 homopolymer Polymers 0.000 description 4
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
230000008646 thermal stress Effects 0.000 description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
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 3
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 3
BITAPBDLHJQAID-KTKRTIGZSA-N 2-[2-hydroxyethyl-[(z)-octadec-9-enyl]amino]ethanol Chemical compound CCCCCCCC\C=C/CCCCCCCCN(CCO)CCO BITAPBDLHJQAID-KTKRTIGZSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
239000004604 Blowing Agent Substances 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
239000004609 Impact Modifier Substances 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
229910019142 PO4 Inorganic materials 0.000 description 3
229920002319 Poly(methyl acrylate) Polymers 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 3
230000002411 adverse Effects 0.000 description 3
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 3
150000007942 carboxylates Chemical class 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
238000000576 coating method Methods 0.000 description 3
238000006731 degradation reaction Methods 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
ZJIPHXXDPROMEF-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O ZJIPHXXDPROMEF-UHFFFAOYSA-N 0.000 description 3
HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 3
UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
238000002845 discoloration Methods 0.000 description 3
239000004815 dispersion polymer Substances 0.000 description 3
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
239000006260 foam Substances 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
238000010348 incorporation Methods 0.000 description 3
230000006698 induction Effects 0.000 description 3
239000004611 light stabiliser Substances 0.000 description 3
239000000395 magnesium oxide Substances 0.000 description 3
230000003287 optical effect Effects 0.000 description 3
239000010452 phosphate Substances 0.000 description 3
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
239000004926 polymethyl methacrylate Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
238000010526 radical polymerization reaction Methods 0.000 description 3
IXGNPUSUVRTQGW-UHFFFAOYSA-M sodium;perchlorate;hydrate Chemical compound O.[Na+].[O-]Cl(=O)(=O)=O IXGNPUSUVRTQGW-UHFFFAOYSA-M 0.000 description 3
229920000638 styrene acrylonitrile Polymers 0.000 description 3
125000005591 trimellitate group Chemical group 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
GWEHVDNNLFDJLR-UHFFFAOYSA-N 1,3-diphenylurea Chemical compound C=1C=CC=CC=1NC(=O)NC1=CC=CC=C1 GWEHVDNNLFDJLR-UHFFFAOYSA-N 0.000 description 2
SPURMHFLEKVAAS-UHFFFAOYSA-N 1-docosene Chemical compound CCCCCCCCCCCCCCCCCCCCC=C SPURMHFLEKVAAS-UHFFFAOYSA-N 0.000 description 2
HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
NDLNTMNRNCENRZ-UHFFFAOYSA-N 2-[2-hydroxyethyl(octadecyl)amino]ethanol Chemical compound CCCCCCCCCCCCCCCCCCN(CCO)CCO NDLNTMNRNCENRZ-UHFFFAOYSA-N 0.000 description 2
WPMYUUITDBHVQZ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoic acid Chemical compound CC(C)(C)C1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-N 0.000 description 2
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
102100035474 DNA polymerase kappa Human genes 0.000 description 2
101710108091 DNA polymerase kappa Proteins 0.000 description 2
BWLUMTFWVZZZND-UHFFFAOYSA-N Dibenzylamine Chemical group C=1C=CC=CC=1CNCC1=CC=CC=C1 BWLUMTFWVZZZND-UHFFFAOYSA-N 0.000 description 2
ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 2
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
229920009204 Methacrylate-butadiene-styrene Polymers 0.000 description 2
239000006057 Non-nutritive feed additive Substances 0.000 description 2
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
229920001944 Plastisol Polymers 0.000 description 2
239000004372 Polyvinyl alcohol Substances 0.000 description 2
KRADHMIOFJQKEZ-UHFFFAOYSA-N Tri-2-ethylhexyl trimellitate Chemical compound CCCCC(CC)COC(=O)C1=CC=C(C(=O)OCC(CC)CCCC)C(C(=O)OCC(CC)CCCC)=C1 KRADHMIOFJQKEZ-UHFFFAOYSA-N 0.000 description 2
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
239000006096 absorbing agent Substances 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
229910000323 aluminium silicate Inorganic materials 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
UJMDYLWCYJJYMO-UHFFFAOYSA-N benzene-1,2,3-tricarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1C(O)=O UJMDYLWCYJJYMO-UHFFFAOYSA-N 0.000 description 2
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WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
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229910052566 spinel group Inorganic materials 0.000 description 1
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150000003918 triazines Chemical class 0.000 description 1
STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
229960001147 triclofos Drugs 0.000 description 1
FICPQAZLPKLOLH-UHFFFAOYSA-N tricyclohexyl phosphite Chemical compound C1CCCCC1OP(OC1CCCCC1)OC1CCCCC1 FICPQAZLPKLOLH-UHFFFAOYSA-N 0.000 description 1
ABVVEAHYODGCLZ-UHFFFAOYSA-N tridecan-1-amine Chemical group CCCCCCCCCCCCCN ABVVEAHYODGCLZ-UHFFFAOYSA-N 0.000 description 1
125000002889 tridecyl 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])[H] 0.000 description 1
JNXDCMUUZNIWPQ-UHFFFAOYSA-N trioctyl benzene-1,2,4-tricarboxylate Chemical compound CCCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCC)C(C(=O)OCCCCCCCC)=C1 JNXDCMUUZNIWPQ-UHFFFAOYSA-N 0.000 description 1
HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 1
IGQFKXMQIMEIJV-UHFFFAOYSA-N tris(11-methyldodecyl) benzene-1,2,4-tricarboxylate Chemical compound CC(C)CCCCCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCCCCC(C)C)C(C(=O)OCCCCCCCCCCC(C)C)=C1 IGQFKXMQIMEIJV-UHFFFAOYSA-N 0.000 description 1
KOWVWXQNQNCRRS-UHFFFAOYSA-N tris(2,4-dimethylphenyl) phosphate Chemical compound CC1=CC(C)=CC=C1OP(=O)(OC=1C(=CC(C)=CC=1)C)OC1=CC=C(C)C=C1C KOWVWXQNQNCRRS-UHFFFAOYSA-N 0.000 description 1
WDRCVXGINNJWPH-UHFFFAOYSA-N tris(6-methylheptyl) benzene-1,2,4-tricarboxylate Chemical compound CC(C)CCCCCOC(=O)C1=CC=C(C(=O)OCCCCCC(C)C)C(C(=O)OCCCCCC(C)C)=C1 WDRCVXGINNJWPH-UHFFFAOYSA-N 0.000 description 1
FJFYFBRNDHRTHL-UHFFFAOYSA-N tris(8-methylnonyl) benzene-1,2,4-tricarboxylate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCC(C)C)C(C(=O)OCCCCCCCC(C)C)=C1 FJFYFBRNDHRTHL-UHFFFAOYSA-N 0.000 description 1
235000013799 ultramarine blue Nutrition 0.000 description 1
QFKMMXYLAPZKIB-UHFFFAOYSA-N undecan-1-amine Chemical group CCCCCCCCCCCN QFKMMXYLAPZKIB-UHFFFAOYSA-N 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
229940005605 valeric acid Drugs 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
FUSUHKVFWTUUBE-UHFFFAOYSA-N vinyl methyl ketone Natural products CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 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
239000000080 wetting agent Substances 0.000 description 1
239000010456 wollastonite Substances 0.000 description 1
229910052882 wollastonite Inorganic materials 0.000 description 1
239000002023 wood Substances 0.000 description 1
DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
229910001928 zirconium oxide Inorganic materials 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

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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- 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
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
- 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
- C08J3/00—Processes of treating or compounding macromolecular substances
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms

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Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Polymerisation Methods In General (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

ZA200405251A 2001-12-04 2004-07-01 Prestabilization of hologen-containing polymers. ZA200405251B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE10159344A DE10159344A1 (de)	2001-12-04	2001-12-04	Prestabilisierung von halogenhaltigen Polymeren

Publications (1)

Publication Number	Publication Date
ZA200405251B true ZA200405251B (en)	2005-06-21

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ZA200405251A ZA200405251B (en)	2001-12-04	2004-07-01	Prestabilization of hologen-containing polymers.

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US (2)	US20040259988A1 (hu)
EP (1)	EP1461375B1 (hu)
KR (1)	KR100896259B1 (hu)
CN (1)	CN1282691C (hu)
AR (1)	AR037616A1 (hu)
AT (1)	ATE456606T1 (hu)
AU (1)	AU2002364387B2 (hu)
BR (1)	BR0214647A (hu)
CA (1)	CA2463471C (hu)
DE (2)	DE10159344A1 (hu)
DK (1)	DK1461375T3 (hu)
ES (1)	ES2340150T3 (hu)
GT (1)	GT200200255A (hu)
HU (1)	HUP0402190A2 (hu)
MX (1)	MXPA04005411A (hu)
NO (1)	NO20042736L (hu)
PL (1)	PL205121B1 (hu)
TW (1)	TWI229088B (hu)
WO (1)	WO2003048232A1 (hu)
ZA (1)	ZA200405251B (hu)

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Publication number	Priority date	Publication date	Assignee	Title
DE10159344A1 (de) *	2001-12-04	2003-06-12	Crompton Vinyl Additives Gmbh	Prestabilisierung von halogenhaltigen Polymeren
DE10356670A1 (de) *	2003-12-04	2005-06-30	Artemis Research Gmbh & Co. Kg	Stabilisatorsystem für halogenhaltige Polymere
US20070254987A1 (en) *	2006-04-26	2007-11-01	Associated Materials, Inc.	Siding panel formed of polymer and wood flour
US20080306187A1 (en) *	2007-06-11	2008-12-11	Festa Daniel E	Siding panel formed of polymer and wood floor
DE102009023651B4 (de) *	2009-05-26	2021-07-01	Aesculap Ag	Verfahren zur Herstellung eines mit einem Stabilisator dotierten Polyethylens und Verwendung eines nach diesem Verfahren hergestellten Polyethylens
EP2357276B2 (de) *	2010-02-01	2016-01-27	Benecke-Kaliko AG	Mehrschichtiges Flächengebilde und Verfahren zu seiner Herstellung
FR2986003B1 (fr) *	2012-01-24	2015-01-16	Arkema France	Procede de preparation de polymeres halogenes
CN104877056B (zh) *	2015-07-02	2017-05-10	杭州电化集团有限公司	一种减少颗粒表面皮膜、提高孔隙率的聚氯乙烯树脂制备方法

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2972617A (en) *	1959-06-10	1961-02-21	Reilly Tar & Chem Corp	N-di-(alkanol-pipecolyl)-alkanol amines
DE1269350B (de)	1963-08-30	1968-05-30	Huels Chemische Werke Ag	Verfahren zur Herstellung von rieselfaehigen, fuer die Hartverarbeitung geeigneten Vinylchloridpolymerisaten durch Suspensionspolymerisation
US3657183A (en) *	1969-04-24	1972-04-18	American Cyanamid Co	Stabilization of poly(vinyl chloride)
US3862066A (en) *	1971-05-26	1975-01-21	Universal Pvc Resins	Method for making rigid vinyl chloride polymer compounds
US4000100A (en) *	1971-06-04	1976-12-28	W. R. Grace & Co.	Thermal and light stabilized polyvinyl chloride resins
US4189550A (en) *	1975-01-31	1980-02-19	Deutsche Gold- Und Silber-Scheindeanstalt Vormals Roessler	Antistatic agents for thermoplastic synthetic resins
US4252705A (en) *	1978-12-26	1981-02-24	Argus Chemical Corporation	Resistance of polyvinyl chloride resins to discoloration during drying with N,N'-diphenyl urea
DE3113442A1 (de) *	1981-04-03	1982-10-21	Henkel KGaA, 4000 Düsseldorf	"stabilisierte polyvinylchlorid-formmassen"
US4624980A (en) *	1984-08-31	1986-11-25	Milliken Research Corporation	N-t-alkyl-N-sec-alkyl secondary amine compounds
JPH0621211B2 (ja) *	1985-08-13	1994-03-23	旭電化工業株式会社	塩化ビニル樹脂組成物
DE3630783A1 (de) *	1986-09-10	1988-03-24	Neynaber Chemie Gmbh	Gleitmittel fuer thermoplastische kunststoffe
US4861816A (en) *	1986-12-29	1989-08-29	Sumitomo Chemical Company	Polyvinyl chloride resin composition for powder molding
JPH0788401B2 (ja)	1987-03-06	1995-09-27	信越化学工業株式会社	塩化ビニル系重合体の製造方法
JP2551802B2 (ja) *	1987-12-29	1996-11-06	日本合成化学工業株式会社	含ハロゲン熱可塑性樹脂組成物
US5034443A (en) *	1990-05-18	1991-07-23	Witco Corporation	Polymer stabilizer and polymer composition stabilized therewith
WO1994024200A1 (en) *	1993-04-16	1994-10-27	Akzo Nobel N.V.	Liquid stabilizer comprising metal soap and solubilized metal perchlorate
MY114466A (en)	1996-09-25	2002-10-31	Crompton Vinyl Additives Gmbh	Rigid pvc stabilised with n, n-dimethyl-6-aminouracils
EP1510545A3 (de) *	1998-06-26	2005-06-15	Wolfgang Dr. Wehner	Oxaalkyl-6-Aminouracile zum Stabilisieren von halogenhaltigen Polymeren
CN1221602C (zh) *	2000-12-13	2005-10-05	克罗姆普顿乙烯添加剂有限公司	用于稳定含卤素聚合物的稳定剂系统
DE10159344A1 (de) *	2001-12-04	2003-06-12	Crompton Vinyl Additives Gmbh	Prestabilisierung von halogenhaltigen Polymeren
DE10301675A1 (de) *	2003-01-17	2004-07-29	Crompton Vinyl Additives Gmbh	Stabilisatorsystem zur PVC-Stabilisierung

2001
- 2001-12-04 DE DE10159344A patent/DE10159344A1/de not_active Ceased
2002
- 2002-11-29 TW TW091134858A patent/TWI229088B/zh not_active IP Right Cessation
- 2002-12-02 ES ES02799735T patent/ES2340150T3/es not_active Expired - Lifetime
- 2002-12-02 PL PL370566A patent/PL205121B1/pl not_active IP Right Cessation
- 2002-12-02 CA CA2463471A patent/CA2463471C/en not_active Expired - Fee Related
- 2002-12-02 CN CNB028243579A patent/CN1282691C/zh not_active Expired - Fee Related
- 2002-12-02 HU HU0402190A patent/HUP0402190A2/hu unknown
- 2002-12-02 AT AT02799735T patent/ATE456606T1/de not_active IP Right Cessation
- 2002-12-02 DE DE60235262T patent/DE60235262D1/de not_active Expired - Lifetime
- 2002-12-02 KR KR1020047007210A patent/KR100896259B1/ko not_active IP Right Cessation
- 2002-12-02 WO PCT/EP2002/013628 patent/WO2003048232A1/en not_active Application Discontinuation
- 2002-12-02 DK DK02799735.2T patent/DK1461375T3/da active
- 2002-12-02 US US10/494,408 patent/US20040259988A1/en not_active Abandoned
- 2002-12-02 AU AU2002364387A patent/AU2002364387B2/en not_active Ceased
- 2002-12-02 EP EP02799735A patent/EP1461375B1/en not_active Revoked
- 2002-12-02 MX MXPA04005411A patent/MXPA04005411A/es active IP Right Grant
- 2002-12-02 BR BR0214647-9A patent/BR0214647A/pt not_active Application Discontinuation
- 2002-12-03 GT GT200200255A patent/GT200200255A/es unknown
- 2002-12-03 AR ARP020104663A patent/AR037616A1/es active IP Right Grant
2004
- 2004-06-29 NO NO20042736A patent/NO20042736L/no not_active Application Discontinuation
- 2004-07-01 ZA ZA200405251A patent/ZA200405251B/en unknown
2007
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Also Published As

Publication number	Publication date
MXPA04005411A (es)	2004-10-11
US20040259988A1 (en)	2004-12-23
EP1461375B1 (en)	2010-01-27
KR20050044428A (ko)	2005-05-12
TWI229088B (en)	2005-03-11
DE10159344A1 (de)	2003-06-12
CA2463471A1 (en)	2003-06-12
US20070299175A1 (en)	2007-12-27
CN1599768A (zh)	2005-03-23
HUP0402190A2 (hu)	2005-01-28
NO20042736L (no)	2004-06-29
AU2002364387B2 (en)	2008-01-03
BR0214647A (pt)	2004-11-03
WO2003048232A1 (en)	2003-06-12
DK1461375T3 (da)	2010-05-10
GT200200255A (es)	2004-01-15
AU2002364387A1 (en)	2003-06-17
TW200300767A (en)	2003-06-16
CA2463471C (en)	2010-04-27
ATE456606T1 (de)	2010-02-15
AR037616A1 (es)	2004-11-17
ES2340150T3 (es)	2010-05-31
KR100896259B1 (ko)	2009-05-08
DE60235262D1 (de)	2010-03-18
PL205121B1 (pl)	2010-03-31
EP1461375A1 (en)	2004-09-29
CN1282691C (zh)	2006-11-01
US7612133B2 (en)	2009-11-03
PL370566A1 (en)	2005-05-30

Publication	Publication Date	Title
CA2429498C (en)	2009-09-08	Stabilizer system for stabilizing halogen-containing polymers
AU2003292262B2 (en)	2009-04-02	Stabilizer system for stabilizing PVC
US7671118B2 (en)	2010-03-02	Stabilizer system for stabilizing halogen-containing polymers
US7612133B2 (en)	2009-11-03	Prestabilization of halogen-containing polymers
US7393887B2 (en)	2008-07-01	Stabilizer system for stabilizing halogen-containing polymers
US20090170988A1 (en)	2009-07-02	Stabilizing system for halogenous polymers
CA2523538C (en)	2012-05-29	Stabiliser system for the stabilisation of halogenated polymers
WO2003048233A1 (en)	2003-06-12	Stabilization of dispersions of halogen-containing polymers