DE2142918A1 - Stabilisatoren für Vinylchlorid ent haltende Polymere - Google Patents

Stabilisatoren für Vinylchlorid ent haltende Polymere

Info

Publication number: DE2142918A1
Authority: DE; Germany
Prior art keywords: lead; basic lead; composition according; polyhydric alcohol; carboxylate
Prior art date: 1970-08-29
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

Application number

DE19712142918

Other languages

German (de)

English (en)

Inventor

Vincent St Helens Hutton Ronald Eric Southport Lancashire lies Brian Rodney Allerton Liverpool Oakes, (Großbritannien)

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Interstab Ltd

Original Assignee

Interstab Ltd

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.)

1970-08-29

Filing date

1971-08-27

Publication date

1972-03-02

1971-08-27 Application filed by Interstab Ltd filed Critical Interstab Ltd

1972-03-02 Publication of DE2142918A1 publication Critical patent/DE2142918A1/de

Status Pending legal-status Critical Current

Links

BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims description 7
239000003381 stabilizer Substances 0.000 title description 27
229920000642 polymer Polymers 0.000 title description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 47
239000000203 mixture Substances 0.000 claims description 29
239000011347 resin Substances 0.000 claims description 23
229920005989 resin Polymers 0.000 claims description 23
150000005846 sugar alcohols Polymers 0.000 claims description 22
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 17
150000007942 carboxylates Chemical class 0.000 claims description 15
239000007795 chemical reaction product Substances 0.000 claims description 12
230000000087 stabilizing effect Effects 0.000 claims description 10
-1 alkylene glycol Chemical compound 0.000 claims description 9
150000001875 compounds Chemical class 0.000 claims description 9
238000000034 method Methods 0.000 claims description 9
229940031826 phenolate Drugs 0.000 claims description 7
150000003839 salts Chemical class 0.000 claims description 6
UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 claims description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
UEQDDJASYZLJFL-UHFFFAOYSA-L diphenoxylead Chemical compound [Pb+2].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 UEQDDJASYZLJFL-UHFFFAOYSA-L 0.000 claims description 4
VLOJXAQYHIVPFI-UHFFFAOYSA-H lead(2+);diacetate;tetrahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[Pb+2].[Pb+2].[Pb+2].CC([O-])=O.CC([O-])=O VLOJXAQYHIVPFI-UHFFFAOYSA-H 0.000 claims description 3
YJOMWQQKPKLUBO-UHFFFAOYSA-L lead(2+);phthalate Chemical compound [Pb+2].[O-]C(=O)C1=CC=CC=C1C([O-])=O YJOMWQQKPKLUBO-UHFFFAOYSA-L 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims description 2
239000000470 constituent Substances 0.000 claims description 2
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 claims 4
KRJUSWXDFZSJQD-UHFFFAOYSA-N benzoic acid;lead Chemical compound [Pb].OC(=O)C1=CC=CC=C1 KRJUSWXDFZSJQD-UHFFFAOYSA-N 0.000 claims 1
239000000047 product Substances 0.000 description 17
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 12
229940046892 lead acetate Drugs 0.000 description 12
239000003086 colorant Substances 0.000 description 9
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 9
PNZVFASWDSMJER-UHFFFAOYSA-N acetic acid;lead Chemical compound [Pb].CC(O)=O PNZVFASWDSMJER-UHFFFAOYSA-N 0.000 description 8
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 8
HEYYNPBHZQPMJJ-UHFFFAOYSA-L dibenzoyloxylead Chemical compound C=1C=CC=CC=1C(=O)O[Pb]OC(=O)C1=CC=CC=C1 HEYYNPBHZQPMJJ-UHFFFAOYSA-L 0.000 description 7
150000003077 polyols Chemical class 0.000 description 7
150000002009 diols Chemical class 0.000 description 6
229920005862 polyol Polymers 0.000 description 6
239000007787 solid Substances 0.000 description 6
150000001298 alcohols Chemical class 0.000 description 5
239000000126 substance Substances 0.000 description 5
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 4
OCWMFVJKFWXKNZ-UHFFFAOYSA-L lead(2+);oxygen(2-);sulfate Chemical compound [O-2].[O-2].[O-2].[Pb+2].[Pb+2].[Pb+2].[Pb+2].[O-]S([O-])(=O)=O OCWMFVJKFWXKNZ-UHFFFAOYSA-L 0.000 description 4
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 4
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 4
YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 3
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 3
150000002611 lead compounds Chemical class 0.000 description 3
PIJPYDMVFNTHIP-UHFFFAOYSA-L lead sulfate Chemical compound [PbH4+2].[O-]S([O-])(=O)=O PIJPYDMVFNTHIP-UHFFFAOYSA-L 0.000 description 3
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 3
230000006641 stabilisation Effects 0.000 description 3
238000011105 stabilization Methods 0.000 description 3
TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
HDIFHQMREAYYJW-XGXNLDPDSA-N Glyceryl Ricinoleate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(=O)OCC(O)CO HDIFHQMREAYYJW-XGXNLDPDSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
229960000583 acetic acid Drugs 0.000 description 2
BGYBTGDDOPTJSB-UHFFFAOYSA-N acetic acid;ethane-1,2-diol Chemical compound CC(O)=O.OCCO BGYBTGDDOPTJSB-UHFFFAOYSA-N 0.000 description 2
ACOGMWBDRJJKNB-UHFFFAOYSA-N acetic acid;ethene Chemical group C=C.CC(O)=O ACOGMWBDRJJKNB-UHFFFAOYSA-N 0.000 description 2
KQNKJJBFUFKYFX-UHFFFAOYSA-N acetic acid;trihydrate Chemical compound O.O.O.CC(O)=O KQNKJJBFUFKYFX-UHFFFAOYSA-N 0.000 description 2
150000004703 alkoxides Chemical class 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
230000018109 developmental process Effects 0.000 description 2
VSFQMZYFJAOOOG-UHFFFAOYSA-N di(propan-2-yloxy)lead Chemical compound CC(C)O[Pb]OC(C)C VSFQMZYFJAOOOG-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
230000002349 favourable effect Effects 0.000 description 2
239000012362 glacial acetic acid Substances 0.000 description 2
229940116338 glyceryl ricinoleate Drugs 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
150000002440 hydroxy compounds Chemical class 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
239000000314 lubricant Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000003756 stirring Methods 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
TUIKVTLNQXJRFO-BTJKTKAUSA-N (z)-but-2-enedioic acid;2-ethyl-2-(hydroxymethyl)propane-1,3-diol Chemical compound OC(=O)\C=C/C(O)=O.CCC(CO)(CO)CO TUIKVTLNQXJRFO-BTJKTKAUSA-N 0.000 description 1
KEQXNNJHMWSZHK-UHFFFAOYSA-L 1,3,2,4$l^{2}-dioxathiaplumbetane 2,2-dioxide Chemical compound [Pb+2].[O-]S([O-])(=O)=O KEQXNNJHMWSZHK-UHFFFAOYSA-L 0.000 description 1
WZUNUACWCJJERC-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CC)(CO)CO WZUNUACWCJJERC-UHFFFAOYSA-N 0.000 description 1
DZCGZGSJEWBGRY-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)CO.OCC(CO)(CO)CO.OCC(CO)(CO)CO DZCGZGSJEWBGRY-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
239000004135 Bone phosphate Substances 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000004606 Fillers/Extenders Substances 0.000 description 1
HSRJKNPTNIJEKV-UHFFFAOYSA-N Guaifenesin Chemical compound COC1=CC=CC=C1OCC(O)CO HSRJKNPTNIJEKV-UHFFFAOYSA-N 0.000 description 1
YBJVKNAWIXTJIO-UHFFFAOYSA-N acetic acid;2-ethyl-2-(hydroxymethyl)propane-1,3-diol Chemical compound CC(O)=O.CCC(CO)(CO)CO YBJVKNAWIXTJIO-UHFFFAOYSA-N 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000032683 aging Effects 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
241001233037 catfish Species 0.000 description 1
238000004040 coloring Methods 0.000 description 1
229940125904 compound 1 Drugs 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000003111 delayed effect Effects 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
230000037213 diet Effects 0.000 description 1
235000005911 diet Nutrition 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000945 filler Substances 0.000 description 1
238000002309 gasification Methods 0.000 description 1
238000000265 homogenisation Methods 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
229910000464 lead oxide Inorganic materials 0.000 description 1
230000007774 longterm Effects 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
235000019645 odor Nutrition 0.000 description 1
YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
150000004707 phenolate Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229920000166 polytrimethylene carbonate Polymers 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000006077 pvc stabilizer Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
238000010792 warming Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/003—Compounds containing elements of Groups 4 or 14 of the Periodic Table without C-Metal linkages
- 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
- C08K5/05—Alcohols; Metal alcoholates
- C08K5/053—Polyhydroxylic alcohols
- 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
- C08K5/13—Phenols; Phenolates
- C08K5/138—Phenolates

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Compositions Of Macromolecular Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DE19712142918 1970-08-29 1971-08-27 Stabilisatoren für Vinylchlorid ent haltende Polymere Pending DE2142918A1 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB4170070A GB1359296A (en)	1970-08-29	1970-08-29	Stabilisers for polymers containing vinyl chloride

Publications (1)

Publication Number	Publication Date
DE2142918A1 true DE2142918A1 (de)	1972-03-02

Family

ID=10420954

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE19712142918 Pending DE2142918A1 (de)	1970-08-29	1971-08-27	Stabilisatoren für Vinylchlorid ent haltende Polymere

Country Status (10)

Country	Link
AT (1)	AT320288B (xx)
AU (1)	AU3263771A (xx)
BE (1)	BE771812A (xx)
CA (1)	CA966143A (xx)
DE (1)	DE2142918A1 (xx)
ES (1)	ES394551A1 (xx)
FR (1)	FR2106130A5 (xx)
GB (1)	GB1359296A (xx)
NL (1)	NL7111602A (xx)
ZA (1)	ZA715483B (xx)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3735863A1 (de) *	1987-10-23	1989-05-03	Metallgesellschaft Ag	3-basisches bleidimethylolpropionat und dieses enthaltende stabilisatorzusammensetzung fuer halogenhaltige vinylpolymerisate
WO1989009758A1 (en) *	1988-04-15	1989-10-19	Ernest Gordon Hallsworth	Formation of complex compounds and polymers between metals and polyhydroxy organic compounds and additions

1970
- 1970-08-29 GB GB4170070A patent/GB1359296A/en not_active Expired
1971
- 1971-08-17 ZA ZA715483A patent/ZA715483B/xx unknown
- 1971-08-23 AU AU32637/71A patent/AU3263771A/en not_active Expired
- 1971-08-24 NL NL7111602A patent/NL7111602A/xx unknown
- 1971-08-24 CA CA121,212A patent/CA966143A/en not_active Expired
- 1971-08-26 BE BE771812A patent/BE771812A/nl unknown
- 1971-08-26 ES ES394551A patent/ES394551A1/es not_active Expired
- 1971-08-27 AT AT752171A patent/AT320288B/de active
- 1971-08-27 FR FR7131131A patent/FR2106130A5/fr not_active Expired
- 1971-08-27 DE DE19712142918 patent/DE2142918A1/de active Pending

Also Published As

Publication number	Publication date
AT320288B (de)	1975-02-10
FR2106130A5 (xx)	1972-04-28
BE771812A (nl)	1971-12-31
ES394551A1 (es)	1974-11-16
GB1359296A (en)	1974-07-10
CA966143A (en)	1975-04-15
ZA715483B (en)	1972-06-28
NL7111602A (xx)	1972-03-02
AU3263771A (en)	1973-03-01

Legal Events

Date	Code	Title	Description
1978-12-07	OHA	Expiration of time for request for examination

Publication	Publication Date	Title
DE2233743A1 (de)	1973-01-25	Stabilisiertes polyvinylchlorid und stabilisierungsmischungen hierfuer
DE2166076A1 (de)	1973-07-19	Dihydroxyspirochromanverbindungen, sowie diese dihydroxyspirochromanverbindungen enthaltende polyesterzusammensetzungen
DE1234023B (de)	1967-02-09	Verfahren zum Stabilisieren von isotaktischem Polypropylen
DE1770823A1 (de)	1972-10-19	Thermoplastische Formmassen aus Blockcopolyestern
DE2022011C3 (de)	1985-01-03	Glycerintrimontanate, Verfahren zu ihrer Herstellung und deren Verwendung
DE2525513A1 (de)	1976-01-02	Stabilisierte polyalkylenharz- gemische
DE1569374A1 (de)	1970-04-09	Polyvinylharz-Stabilisatorsysteme und mit diesen stabilisierte Harzmassen
DE2623985A1 (de)	1977-12-08	Neue organische phosphite und ihre verwendung als stabilisatoren
DE1669841C3 (de)	1974-01-03	Verfahren zur Herstellung von Mercaptogruppen enthaltenden Organozinnverbindungen
DE2532066C2 (de)	1986-12-04	Polyester-Formmasse und ihre Verwendung
DE2509552C2 (de)	1984-08-09	Terephthalat von 2,2'-Methylen-bis(4-methyl-6-tert.-butylphenol) sowie dessen Verwendung
DE2305270C3 (de)	1980-10-30	Verfahren zum Herstellen von PoIysiloxanelastomeren bei Raumtemperatur
DE1958744B2 (de)	1978-02-09	Dialkylzinndimercaptoverbindungen deren herstellung und verwendung
DE2142918A1 (de)	1972-03-02	Stabilisatoren für Vinylchlorid ent haltende Polymere
DE2523909A1 (de)	1976-12-09	Physiologisch unbedenkliche stabilisatorkombinationen fuer halogenierte polyolefine
DE2719526A1 (de)	1977-12-15	Organo-zinn-verbindungen und deren verwendung
DE1569009A1 (de)	1970-09-10	Stabilisierungsmittel fuer Vinylhalogenidharzmassen
DE1219223C2 (de)	1973-11-15	Stabilisierung von Vinylhalogenidpolymerisaten und -mischpolymerisaten
DE2521937A1 (de)	1976-01-02	Antistrukturmittel
DE1569011B2 (de)	1976-10-07	Stabilisierungsmittel fuer vinylhalogenidpolymerisate
DE2523910C3 (de)	1981-04-16	Neue organische Phosphite und ihre Verwendung als Stabilisatoren
DE2456278C3 (de)	1979-08-30	Thermoplastische transparente und schlagfeste Masse auf der Grundlage von Vinylchlorid-Polymerisaten
DE2015273B2 (de)	1974-04-11	Weichgemachte Präparate
DE1694560A1 (de)	1971-08-12	Verfahren zur Herstellung von flammwidrigen,insbesondere unbrennbaren Polyurethan-Schaumstoffen
DE1141785B (de)	1962-12-27	Stabilisierte Formmassen auf Basis von Polyaethylen