DE2303179A1 - Waermestabilisiertes polymeres - Google Patents
Waermestabilisiertes polymeresInfo
- Publication number
- DE2303179A1 DE2303179A1 DE2303179A DE2303179A DE2303179A1 DE 2303179 A1 DE2303179 A1 DE 2303179A1 DE 2303179 A DE2303179 A DE 2303179A DE 2303179 A DE2303179 A DE 2303179A DE 2303179 A1 DE2303179 A1 DE 2303179A1
- Authority
- DE
- Germany
- Prior art keywords
- acid
- polymer
- thioglycolate
- moles
- component
- 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.)
- Pending
Links
- 239000003381 stabilizer Substances 0.000 claims description 50
- 229920000642 polymer Polymers 0.000 claims description 26
- 238000011065 in-situ storage Methods 0.000 claims description 15
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 claims description 13
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 12
- 230000006641 stabilisation Effects 0.000 claims description 12
- 238000011105 stabilization Methods 0.000 claims description 12
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 11
- IUNVCWLKOOCPIT-UHFFFAOYSA-N 6-methylheptylsulfanyl 2-hydroxyacetate Chemical compound CC(C)CCCCCSOC(=O)CO IUNVCWLKOOCPIT-UHFFFAOYSA-N 0.000 claims description 10
- 230000015556 catabolic process Effects 0.000 claims description 9
- 238000006731 degradation reaction Methods 0.000 claims description 9
- PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 claims description 8
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 8
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 8
- 239000011976 maleic acid Substances 0.000 claims description 8
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 claims description 8
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- 239000005639 Lauric acid Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 claims description 6
- IIPCXIGUIPAGQB-OUKQBFOZSA-N (e)-4-dodecoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCCCCCOC(=O)\C=C\C(O)=O IIPCXIGUIPAGQB-OUKQBFOZSA-N 0.000 claims description 5
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 4
- YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 claims description 4
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 4
- ZHUWXKIPGGZNJW-UHFFFAOYSA-N 6-methylheptyl 3-sulfanylpropanoate Chemical compound CC(C)CCCCCOC(=O)CCS ZHUWXKIPGGZNJW-UHFFFAOYSA-N 0.000 claims description 4
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 4
- 239000005642 Oleic acid Substances 0.000 claims description 4
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 4
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 4
- JQTFPHLEQLLQOT-UHFFFAOYSA-N octadecyl 2-sulfanylacetate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CS JQTFPHLEQLLQOT-UHFFFAOYSA-N 0.000 claims description 4
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 4
- NBOMNTLFRHMDEZ-UHFFFAOYSA-N thiosalicylic acid Chemical compound OC(=O)C1=CC=CC=C1S NBOMNTLFRHMDEZ-UHFFFAOYSA-N 0.000 claims description 4
- BANFORNDDZWGFX-UHFFFAOYSA-N tridecyl 2-sulfanylacetate Chemical compound CCCCCCCCCCCCCOC(=O)CS BANFORNDDZWGFX-UHFFFAOYSA-N 0.000 claims description 4
- MJNLAPRQQJZBQN-UHFFFAOYSA-N tridecyl 3-sulfanylpropanoate Chemical compound CCCCCCCCCCCCCOC(=O)CCS MJNLAPRQQJZBQN-UHFFFAOYSA-N 0.000 claims description 4
- PSYGHMBJXWRQFD-UHFFFAOYSA-N 2-(2-sulfanylacetyl)oxyethyl 2-sulfanylacetate Chemical compound SCC(=O)OCCOC(=O)CS PSYGHMBJXWRQFD-UHFFFAOYSA-N 0.000 claims description 3
- 229920006237 degradable polymer Polymers 0.000 claims description 3
- NKHAVTQWNUWKEO-UHFFFAOYSA-N fumaric acid monomethyl ester Natural products COC(=O)C=CC(O)=O NKHAVTQWNUWKEO-UHFFFAOYSA-N 0.000 claims description 3
- 150000002334 glycols Chemical class 0.000 claims description 3
- NKHAVTQWNUWKEO-IHWYPQMZSA-N methyl hydrogen fumarate Chemical compound COC(=O)\C=C/C(O)=O NKHAVTQWNUWKEO-IHWYPQMZSA-N 0.000 claims description 3
- RJGHQTVXGKYATR-UHFFFAOYSA-L dibutyl(dichloro)stannane Chemical compound CCCC[Sn](Cl)(Cl)CCCC RJGHQTVXGKYATR-UHFFFAOYSA-L 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 claims 6
- UBUWMRSBMYUJAP-UHFFFAOYSA-N s-dodecanoyl dodecanethioate Chemical compound CCCCCCCCCCCC(=O)SC(=O)CCCCCCCCCCC UBUWMRSBMYUJAP-UHFFFAOYSA-N 0.000 claims 3
- NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 0.000 claims 3
- 229910000765 intermetallic Inorganic materials 0.000 claims 2
- 150000002902 organometallic compounds Chemical class 0.000 claims 2
- 239000000178 monomer Substances 0.000 claims 1
- 239000004800 polyvinyl chloride Substances 0.000 description 55
- 229920000915 polyvinyl chloride Polymers 0.000 description 54
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 32
- 229920002554 vinyl polymer Polymers 0.000 description 14
- 239000000203 mixture Substances 0.000 description 11
- -1 dibutyltin glycol dimer Chemical class 0.000 description 10
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 7
- 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 7
- 230000000087 stabilizing effect Effects 0.000 description 6
- ZBBLRPRYYSJUCZ-GRHBHMESSA-L (z)-but-2-enedioate;dibutyltin(2+) Chemical compound [O-]C(=O)\C=C/C([O-])=O.CCCC[Sn+2]CCCC ZBBLRPRYYSJUCZ-GRHBHMESSA-L 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 5
- 229920001155 polypropylene Polymers 0.000 description 5
- 239000012429 reaction media Substances 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 4
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 4
- LQRUPWUPINJLMU-UHFFFAOYSA-N dioctyl(oxo)tin Chemical compound CCCCCCCC[Sn](=O)CCCCCCCC LQRUPWUPINJLMU-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- VNPRJHMMOKDEDZ-UHFFFAOYSA-L 6-methylheptyl 2-[dibutyl-[2-(6-methylheptoxy)-2-oxoethyl]sulfanylstannyl]sulfanylacetate Chemical compound CC(C)CCCCCOC(=O)CS[Sn](CCCC)(CCCC)SCC(=O)OCCCCCC(C)C VNPRJHMMOKDEDZ-UHFFFAOYSA-L 0.000 description 3
- YLFRJROMPGNJRP-UHFFFAOYSA-L [dibutyl(3-sulfanylpropanoyloxy)stannyl] 3-sulfanylpropanoate Chemical compound [O-]C(=O)CCS.[O-]C(=O)CCS.CCCC[Sn+2]CCCC YLFRJROMPGNJRP-UHFFFAOYSA-L 0.000 description 3
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000012975 dibutyltin dilaurate Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- KELBPZSRZMWPAU-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;dibutyltin Chemical compound CCCC[Sn]CCCC.OCC(CO)(CO)CO KELBPZSRZMWPAU-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 230000001588 bifunctional effect Effects 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000013585 weight reducing agent Substances 0.000 description 2
- UKDKWYQGLUUPBF-UHFFFAOYSA-N 1-ethenoxyhexadecane Chemical compound CCCCCCCCCCCCCCCCOC=C UKDKWYQGLUUPBF-UHFFFAOYSA-N 0.000 description 1
- IRIAEMUUDSWZOX-UHFFFAOYSA-L 2,2-dibutyl-1,3,2-oxathiastanninan-6-one Chemical compound CCCC[Sn]1(CCCC)OC(=O)CCS1 IRIAEMUUDSWZOX-UHFFFAOYSA-L 0.000 description 1
- LVYHWZLVISKZHG-UHFFFAOYSA-L 2-(2,2-dibutyl-5-oxo-1,3,2-oxathiastannolan-4-yl)acetic acid Chemical compound CCCC[Sn]1(CCCC)OC(=O)CC(C(O)=O)S1 LVYHWZLVISKZHG-UHFFFAOYSA-L 0.000 description 1
- 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 1
- ISPPPVFAJYEEGT-UHFFFAOYSA-L 2-carboxybenzenethiolate dioctyltin(2+) Chemical compound [O-]C(=O)c1ccccc1S.[O-]C(=O)c1ccccc1S.CCCCCCCC[Sn++]CCCCCCCC ISPPPVFAJYEEGT-UHFFFAOYSA-L 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- 241000252505 Characidae Species 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241001293250 Lagascea decipiens Species 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- PZGVVCOOWYSSGB-UHFFFAOYSA-L but-2-enedioate;dioctyltin(2+) Chemical compound CCCCCCCC[Sn]1(CCCCCCCC)OC(=O)C=CC(=O)O1 PZGVVCOOWYSSGB-UHFFFAOYSA-L 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- VVKVIDFEFWYOLN-UHFFFAOYSA-L dibutyltin(2+);2-sulfanylpropanoate Chemical compound CC(S)C([O-])=O.CC(S)C([O-])=O.CCCC[Sn+2]CCCC VVKVIDFEFWYOLN-UHFFFAOYSA-L 0.000 description 1
- IESWIBSMHJCJAG-UHFFFAOYSA-L dibutyltin(2+);8-methyl-2-(6-methylheptyl)-2-sulfanylnonanoate Chemical compound CCCC[Sn+2]CCCC.CC(C)CCCCCC(S)(C([O-])=O)CCCCCC(C)C.CC(C)CCCCCC(S)(C([O-])=O)CCCCCC(C)C IESWIBSMHJCJAG-UHFFFAOYSA-L 0.000 description 1
- ZXDVQYBUEVYUCG-UHFFFAOYSA-N dibutyltin(2+);methanolate Chemical compound CCCC[Sn](OC)(OC)CCCC ZXDVQYBUEVYUCG-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- BLCTWBJQROOONQ-UHFFFAOYSA-N ethenyl prop-2-enoate Chemical compound C=COC(=O)C=C BLCTWBJQROOONQ-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000010952 in-situ formation Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- SJOCPYUKFOTDAN-ZSOIEALJSA-N methyl (4z)-4-hydroxyimino-6,6-dimethyl-3-methylsulfanyl-5,7-dihydro-2-benzothiophene-1-carboxylate Chemical compound C1C(C)(C)C\C(=N\O)C=2C1=C(C(=O)OC)SC=2SC SJOCPYUKFOTDAN-ZSOIEALJSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000013872 montan acid ester Nutrition 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000012747 synergistic agent Substances 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
-
- 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
- C08J3/20—Compounding polymers with additives, e.g. colouring
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyethers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22624572A | 1972-02-14 | 1972-02-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2303179A1 true DE2303179A1 (de) | 1973-08-23 |
Family
ID=22848137
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2303179A Pending DE2303179A1 (de) | 1972-02-14 | 1973-01-23 | Waermestabilisiertes polymeres |
Country Status (10)
| Country | Link |
|---|---|
| JP (1) | JPS4893638A (enExample) |
| AR (1) | AR193333A1 (enExample) |
| AU (1) | AU5123073A (enExample) |
| BE (1) | BE794869A (enExample) |
| BR (1) | BR7300873D0 (enExample) |
| DE (1) | DE2303179A1 (enExample) |
| FR (1) | FR2177727A1 (enExample) |
| IT (1) | IT977053B (enExample) |
| NL (1) | NL7302075A (enExample) |
| ZA (1) | ZA73381B (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0577554A1 (de) * | 1992-06-30 | 1994-01-05 | Ciba-Geigy Ag | Verfahren zur Herstellung von Diorganozinndicarboxylaten |
| DE4420916C1 (de) * | 1994-06-16 | 1995-07-27 | Metallgesellschaft Ag | Diorganylzinnoxid-Phtalsäurediester-Komplexe sowie Verfahren zu ihrer Herstellung und Verwendung der hergestellten Erzeugnisse |
| FR2815632A1 (fr) * | 2000-10-24 | 2002-04-26 | Atofina | Composition a base de maleates d'organoetain, son procede d'obtention et son utilisation pour stabiliser des polymeres thermoplastiques |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS52115849A (en) * | 1976-03-25 | 1977-09-28 | Chugoku Marine Paints | Method of preventing rubber oxidation |
| US4228066A (en) * | 1979-04-12 | 1980-10-14 | Exxon Research & Engineering Co. | Stabilized polymer compositions |
| JPS5915444A (ja) * | 1982-07-20 | 1984-01-26 | Mitsubishi Rayon Co Ltd | 熱安定性メタクリル樹脂組成物 |
| JPS6013849A (ja) * | 1983-07-01 | 1985-01-24 | Katsuta Kako Kk | 含ハロゲン樹脂用安定剤組成物 |
| EP0446174B1 (de) * | 1990-03-09 | 1998-04-22 | Ciba SC Holding AG | Verfahren zur Herstellung eines Stabilisators für halogenhaltige Polymere |
-
0
- BE BE794869D patent/BE794869A/xx unknown
-
1973
- 1973-01-18 ZA ZA730381A patent/ZA73381B/xx unknown
- 1973-01-18 AU AU51230/73A patent/AU5123073A/en not_active Expired
- 1973-01-23 DE DE2303179A patent/DE2303179A1/de active Pending
- 1973-01-25 IT IT47894/73A patent/IT977053B/it active
- 1973-01-29 FR FR7303022A patent/FR2177727A1/fr active Granted
- 1973-01-31 AR AR246361A patent/AR193333A1/es active
- 1973-02-06 BR BR73873A patent/BR7300873D0/pt unknown
- 1973-02-13 JP JP48017840A patent/JPS4893638A/ja active Pending
- 1973-02-14 NL NL7302075A patent/NL7302075A/xx unknown
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0577554A1 (de) * | 1992-06-30 | 1994-01-05 | Ciba-Geigy Ag | Verfahren zur Herstellung von Diorganozinndicarboxylaten |
| US5364954A (en) * | 1992-06-30 | 1994-11-15 | Ciba-Geigy Corporation | Process for the preparation of diorganotin dicarboxylates |
| DE4420916C1 (de) * | 1994-06-16 | 1995-07-27 | Metallgesellschaft Ag | Diorganylzinnoxid-Phtalsäurediester-Komplexe sowie Verfahren zu ihrer Herstellung und Verwendung der hergestellten Erzeugnisse |
| FR2815632A1 (fr) * | 2000-10-24 | 2002-04-26 | Atofina | Composition a base de maleates d'organoetain, son procede d'obtention et son utilisation pour stabiliser des polymeres thermoplastiques |
| EP1201707A1 (fr) * | 2000-10-24 | 2002-05-02 | Atofina | Composition à base de maléates d'organoétain, son procédé d'obtention et son utilisation pour stabiliser des polymeres thermoplastiques |
Also Published As
| Publication number | Publication date |
|---|---|
| BE794869A (fr) | 1973-05-29 |
| NL7302075A (enExample) | 1973-08-16 |
| ZA73381B (en) | 1973-10-31 |
| JPS4893638A (enExample) | 1973-12-04 |
| FR2177727A1 (en) | 1973-11-09 |
| FR2177727B1 (enExample) | 1976-09-10 |
| AR193333A1 (es) | 1973-04-11 |
| BR7300873D0 (pt) | 1973-09-27 |
| IT977053B (it) | 1974-09-10 |
| AU5123073A (en) | 1974-07-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2233743A1 (de) | Stabilisiertes polyvinylchlorid und stabilisierungsmischungen hierfuer | |
| DE2356625C2 (de) | Stabilisierungsmittel | |
| DE2540066B2 (de) | Synergistische Stabilisatorkombination und diese enthaltende Polymerisatmassen auf Vinylhalogenidbasis | |
| DE69624478T2 (de) | Thermisch stabile antistatische agenzien | |
| DE2303179A1 (de) | Waermestabilisiertes polymeres | |
| DE2802531C2 (enExample) | ||
| DE2501331B2 (de) | Verpackungsmaterial aus Vinylchloridpolymeren oder -copolymeren | |
| DE1694981B2 (de) | Verwendung eines festen stabilisators zum stabilisieren von formmassen auf der basis von vinylhalogenidpolymerisaten gegen waerme und licht | |
| DE3125376A1 (de) | Thermoplastische formmassen auf der basis von vinylchloridpolymerisaten und schlagzaehmodifizierungspolymeren | |
| DE2703904C3 (de) | Synergistische Stabilisatorkombination und diese enthaltende Polymermaterialien auf Vinylhalogenidbasis | |
| DE1958744A1 (de) | Stabilisierung von Vinylpolymeren | |
| DE1083541B (de) | Verfahren zum Stabilisieren von Polyvinylchlorid enthaltenden Kunstharzmassen | |
| DE2455614A1 (de) | Stabilisierung von halogen-enthaltenden polymeren | |
| DE1219223C2 (de) | Stabilisierung von Vinylhalogenidpolymerisaten und -mischpolymerisaten | |
| DE1668701B2 (de) | Waermestabile halogenhaltige polymerisatmassen | |
| DE2456278C3 (de) | Thermoplastische transparente und schlagfeste Masse auf der Grundlage von Vinylchlorid-Polymerisaten | |
| DE1544960B2 (de) | Stabilisierte halogenhaltige vinylpolymensate | |
| DE1768208B2 (de) | Hochmolekulare, feste organische Zinnverbindungen | |
| DE1806494C2 (de) | Stabilisatormischung für Halogen enthaltende Polymere | |
| DE1668701C3 (de) | Wärmestabile halogenhaltige Polymerisatmassen | |
| DE940065C (de) | Verfahren zur Stabilisierung von Vinylharz- und von Kautschukerzeugnissen | |
| DE1494171C (de) | Stabilisieren von chlorhaltigen Polymerisaten | |
| DE1194575B (de) | Flammfeste, transparente Formkoerper liefernde Kunststofformmassen | |
| DE4221285C2 (de) | Flammschutzmittel und deren Verwendung | |
| DE1296799B (de) | Weichmacher fuer Vinylchloridpolymerisate |