NO764340L - Fremgangsm}te for stabilisering av sammensetninger p} basis av vinylkloridpolymerer - Google Patents

Fremgangsm}te for stabilisering av sammensetninger p} basis av vinylkloridpolymerer

Info

Publication number: NO764340L
Authority: NO; Norway
Prior art keywords: carbon atoms; vinyl chloride; group containing; compositions; copolymer
Prior art date: 1976-05-10

Application number

NO764340A

Other languages

English (en)

Norwegian (no)

Inventor

Michel Crochemore

Michel Gay

Original Assignee

Rhone Poulenc Ind

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.)

1976-05-10

Filing date

1976-12-22

Publication date

1977-11-11

1976-12-22 Application filed by Rhone Poulenc Ind filed Critical Rhone Poulenc Ind

1977-11-11 Publication of NO764340L publication Critical patent/NO764340L/no

Links

239000000203 mixture Substances 0.000 title claims description 35
229920000642 polymer Polymers 0.000 title claims description 18
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims description 17
238000000034 method Methods 0.000 title claims description 9
230000006641 stabilisation Effects 0.000 title description 3
238000011105 stabilization Methods 0.000 title description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 17
229920001577 copolymer Polymers 0.000 claims description 12
125000000217 alkyl group Chemical group 0.000 claims description 10
150000003839 salts Chemical class 0.000 claims description 10
125000003342 alkenyl group Chemical group 0.000 claims description 6
125000003118 aryl group Chemical group 0.000 claims description 6
150000002894 organic compounds Chemical class 0.000 claims description 5
230000000087 stabilizing effect Effects 0.000 claims description 5
239000003795 chemical substances by application Substances 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
229910052751 metal Inorganic materials 0.000 claims description 4
239000002184 metal Substances 0.000 claims description 4
239000000178 monomer Substances 0.000 claims description 3
125000003710 aryl alkyl group Chemical group 0.000 claims description 2
150000001661 cadmium Chemical class 0.000 claims description 2
159000000007 calcium salts Chemical class 0.000 claims description 2
239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 2
150000007524 organic acids Chemical class 0.000 claims description 2
235000005985 organic acids Nutrition 0.000 claims description 2
150000003751 zinc Chemical class 0.000 claims description 2
MJDMFCNBBJYPMH-UHFFFAOYSA-N 1-phenyltriacontane-1,3-dione Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)CC(=O)C1=CC=CC=C1 MJDMFCNBBJYPMH-UHFFFAOYSA-N 0.000 claims 1
159000000009 barium salts Chemical class 0.000 claims 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
239000003381 stabilizer Substances 0.000 description 11
238000002156 mixing Methods 0.000 description 7
-1 diacetates Chemical class 0.000 description 6
150000001875 compounds Chemical class 0.000 description 5
229920000915 polyvinyl chloride Polymers 0.000 description 5
239000004800 polyvinyl chloride Substances 0.000 description 5
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
229920001519 homopolymer Polymers 0.000 description 4
239000000314 lubricant Substances 0.000 description 4
238000004383 yellowing Methods 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
239000000654 additive Substances 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
238000005096 rolling process Methods 0.000 description 3
238000010557 suspension polymerization reaction Methods 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 3
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
ZKHOYAKAFALNQD-UHFFFAOYSA-N Octacosanoic acid methyl ester Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC ZKHOYAKAFALNQD-UHFFFAOYSA-N 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
238000007664 blowing Methods 0.000 description 2
239000008116 calcium stearate Substances 0.000 description 2
235000013539 calcium stearate Nutrition 0.000 description 2
238000003490 calendering Methods 0.000 description 2
239000000945 filler Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000004570 mortar (masonry) Substances 0.000 description 2
239000000049 pigment Substances 0.000 description 2
229910052573 porcelain Inorganic materials 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000011347 resin Substances 0.000 description 2
229920005989 resin Polymers 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
239000000126 substance Substances 0.000 description 2
KIHBGTRZFAVZRV-UHFFFAOYSA-N 2-hydroxyoctadecanoic acid Chemical class CCCCCCCCCCCCCCCCC(O)C(O)=O KIHBGTRZFAVZRV-UHFFFAOYSA-N 0.000 description 1
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical class [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
241001131688 Coracias garrulus Species 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
229910052788 barium Inorganic materials 0.000 description 1
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical class [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 1
150000001558 benzoic acid derivatives Chemical class 0.000 description 1
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 1
238000012662 bulk polymerization Methods 0.000 description 1
229910052793 cadmium Inorganic materials 0.000 description 1
BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
238000007720 emulsion polymerization reaction Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
SHZIWNPUGXLXDT-UHFFFAOYSA-N ethyl hexanoate Chemical class CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
229920005570 flexible polymer Polymers 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
238000001746 injection moulding Methods 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
150000002689 maleic acids Chemical class 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
239000000155 melt Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000004452 microanalysis Methods 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
238000006053 organic reaction Methods 0.000 description 1
150000002942 palmitic acid derivatives Chemical class 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
229910000104 sodium hydride Inorganic materials 0.000 description 1
239000012312 sodium hydride Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000035900 sweating Effects 0.000 description 1
238000001308 synthesis method Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
238000005979 thermal decomposition reaction Methods 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
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
- C07C45/455—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation with carboxylic acids or their derivatives
- 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
- C08K5/07—Aldehydes; Ketones
- 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

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)
Laminated Bodies (AREA)

NO764340A 1976-05-10 1976-12-22 Fremgangsm}te for stabilisering av sammensetninger p} basis av vinylkloridpolymerer NO764340L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR7614863A FR2351149A2 (fr)	1976-05-10	1976-05-10	Compositions stabilisees a base de chlorure de polyvinyle

Publications (1)

Publication Number	Publication Date
NO764340L true NO764340L (no)	1977-11-11

Family

ID=9173240

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO764340A NO764340L (no)	1976-05-10	1976-12-22	Fremgangsm}te for stabilisering av sammensetninger p} basis av vinylkloridpolymerer

Country Status (18)

Country	Link
JP (1)	JPS52136248A (de)
AT (1)	AT346076B (de)
AU (1)	AU2016776A (de)
BE (1)	BE848449R (de)
CH (1)	CH609078A5 (de)
DD (1)	DD127312A6 (de)
DE (1)	DE2652408C3 (de)
DK (1)	DK574876A (de)
FI (1)	FI763315A (de)
FR (1)	FR2351149A2 (de)
GB (1)	GB1532319A (de)
IT (1)	IT1123634B (de)
LU (1)	LU76199A1 (de)
NL (1)	NL167452C (de)
NO (1)	NO764340L (de)
NZ (1)	NZ182753A (de)
SE (1)	SE415569B (de)
ZA (1)	ZA767150B (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS559664A (en) *	1978-07-07	1980-01-23	Adeka Argus Chem Co Ltd	Stabilized halogen-containing resin composition
FR2456132A2 (fr) *	1979-05-10	1980-12-05	Rhone Poulenc Ind	Compositions stabilisees a base de chlorure de polyvinyle
JP2623271B2 (ja) *	1987-12-20	1997-06-25	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

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2307075A (en) *	1940-08-02	1943-01-05	Carbide And Carbon Chemicais C	Vinyl resin composition
US2669548A (en) *	1951-01-02	1954-02-16	Monsanto Chemicals	Stabilized halogen-containing resins
GB1054585A (de) *	1963-07-02
NL131106C (de) *	1964-01-22
FR1480549A (fr) *	1965-05-21	1967-05-12	Carlisle Chemical Works	Compositions résineuses stabilisées contenant des composés métalliques
CH464521A (de) *	1965-05-21	1968-10-31	Carlisle Chemical Works	Verfahren zur Aufhebung der Lichtempfindlichkeit von plastischen Massen, die Antimon- oder Wismutverbindungen enthalten
US3492267A (en) *	1966-12-02	1970-01-27	Grace W R & Co	Stabilizing poly(vinyl chloride)
CS196295B2 (en) *	1975-01-10	1980-03-31	Rhone Poulenc Ind	Stabilized materials based on polymers or copolymers vinylchloride
FR2324681A2 (fr) *	1975-09-22	1977-04-15	Rhone Poulenc Ind	Compositions stabilisees a base de chlorure de polyvinyle
FR2297227A1 (fr) *	1975-01-10	1976-08-06	Rhone Poulenc Ind	Compositions stabilisees a base de chlorure de polyvinyle

1976
- 1976-05-10 FR FR7614863A patent/FR2351149A2/fr active Granted
- 1976-11-15 LU LU76199A patent/LU76199A1/xx unknown
- 1976-11-17 BE BE172456A patent/BE848449R/xx not_active IP Right Cessation
- 1976-11-17 DE DE2652408A patent/DE2652408C3/de not_active Expired
- 1976-11-18 FI FI763315A patent/FI763315A/fi not_active Application Discontinuation
- 1976-11-19 CH CH1459076A patent/CH609078A5/xx not_active IP Right Cessation
- 1976-11-23 NL NL7613051.A patent/NL167452C/xx not_active IP Right Cessation
- 1976-11-24 GB GB49009/76A patent/GB1532319A/en not_active Expired
- 1976-11-25 DD DD195965A patent/DD127312A6/xx unknown
- 1976-11-29 NZ NZ182753A patent/NZ182753A/xx unknown
- 1976-11-29 IT IT29903/76A patent/IT1123634B/it active
- 1976-11-30 ZA ZA00767150A patent/ZA767150B/xx unknown
- 1976-12-01 AU AU20167/76A patent/AU2016776A/en not_active Expired
- 1976-12-01 AT AT891376A patent/AT346076B/de active
- 1976-12-15 SE SE7614121A patent/SE415569B/xx unknown
- 1976-12-21 DK DK574876A patent/DK574876A/da unknown
- 1976-12-22 NO NO764340A patent/NO764340L/no unknown
1977
- 1977-01-31 JP JP962077A patent/JPS52136248A/ja active Pending

Also Published As

Publication number	Publication date
NL7613051A (nl)	1977-11-14
DE2652408A1 (de)	1977-11-17
LU76199A1 (de)	1977-12-13
ATA891376A (de)	1978-02-15
AT346076B (de)	1978-10-25
NL167452C (nl)	1981-12-16
ZA767150B (en)	1978-08-30
FR2351149A2 (fr)	1977-12-09
BE848449R (fr)	1977-05-17
NL167452B (nl)	1981-07-16
DK574876A (da)	1977-11-11
FR2351149B2 (de)	1980-09-19
SE7614121L (sv)	1977-11-11
AU2016776A (en)	1978-06-08
NZ182753A (en)	1979-12-11
GB1532319A (en)	1978-11-15
SE415569B (sv)	1980-10-13
DE2652408B2 (de)	1978-09-14
IT1123634B (it)	1986-04-30
DD127312A6 (de)	1977-09-14
FI763315A (de)	1977-11-11
DE2652408C3 (de)	1986-03-27
JPS52136248A (en)	1977-11-14
CH609078A5 (en)	1979-02-15

Publication	Publication Date	Title
US4123400A (en)	1978-10-31	Heat-stabilized PVC compositions
NO152094B (no)	1985-04-22	Varmestabilisert vinylkloridplast
DE3784566T2 (de)	1993-07-15	Bisphenolverbindungen enthaltende zusammensetzungen.
NO772264L (no)	1977-12-29	Mykgjorte og stabiliserte sammensetninger p} basis av polyvinylklorid
NO146712B (no)	1982-08-16	Varmestabilisert vinylkloridplast
US4267083A (en)	1981-05-12	Heat-stabilized vinyl chloride polymers
US2972595A (en)	1961-02-21	Dialkyl tin epoxy-succinate stabilizers for polymers of polyvinyl chloride
NO764340L (no)	1977-11-11	Fremgangsm}te for stabilisering av sammensetninger p} basis av vinylkloridpolymerer
US4035559A (en)	1977-07-12	Novel aromatic polyvinyl compounds
US2770611A (en)	1956-11-13	Halogenated polymers stabilized with a hexaorganodistannoxane
EP0113042B1 (de)	1989-08-30	3,4-Dihydro-2H-benzopyran-Derivate, Verfahren zu deren Herstellung, Verfahren zu deren Verwendung als Stabilisator für organische Stoffe und diese Stabilisatoren enthaltende organische Zusammensetzungen
US2628211A (en)	1953-02-10	Polyvinyl chloride resins stabilized with polystannoxanediol esters
US2532018A (en)	1950-11-28	Plasticized resin compositions
US3544502A (en)	1970-12-01	Latex stabilized with salts of polymethylated muconic acids
US4346188A (en)	1982-08-24	Polyolefin compositions stabilized against UV-radiations by pyrrolidine derivatives
US3047611A (en)	1962-07-31	Vinyl 2,2-dihalocyclopropyl carboxylates
US2894022A (en)	1959-07-07	Diesters of aliphatic dicarboxylic acids and hydroxy benzophenones
US3265736A (en)	1966-08-09	4, 4-diamino-nu-methyldiphenylamines
US4405758A (en)	1983-09-20	Vulcanizable acrylate rubber compositions
US3050783A (en)	1962-08-28	Process for stabilizing vinyl chloride polymers
NO144971B (no)	1981-09-07	Varmestabilisert vinylkloridplast inneholdende laktonforbindelser som stabiliseringsmiddel
US2667504A (en)	1954-01-26	Trialkyl-1-benzoylpropane-1,2,3-tricarboxylates and process of preparing same
US2617778A (en)	1952-11-11	Plasticized polymers
US2943076A (en)	1960-06-28	Haloethylene polymers stabilized with diesters of aliphatic dicarboxylic acids and hydroxy benzophenones
GB1582280A (en)	1981-01-07	Process for stabilizing impact-resistant plastics