NO753010L - - Google Patents

Info

Publication number: NO753010L
Authority: NO; Norway
Prior art keywords: polyolefin; carbon atoms; acid; compounds; polyolefins
Prior art date: 1974-09-04

Application number

NO753010A

Other languages

English (en)

Norwegian (no)

Inventor

R Heinrich

H-J Kleiner

Original Assignee

Hoechst Ag

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.)

1974-09-04

Filing date

1975-09-02

Publication date

1976-03-05

1974-09-04 Priority claimed from DE19742442390 external-priority patent/DE2442390C3/de

1975-09-02 Application filed by Hoechst Ag filed Critical Hoechst Ag

1976-03-05 Publication of NO753010L publication Critical patent/NO753010L/no

Links

229920000098 polyolefin Polymers 0.000 claims description 22
-1 diphosphonic acid compound Chemical class 0.000 claims description 10
239000003381 stabilizer Substances 0.000 claims description 9
239000002253 acid Substances 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 4
125000002877 alkyl aryl group Chemical group 0.000 claims description 2
125000002947 alkylene group Chemical group 0.000 claims description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
229910052751 metal Inorganic materials 0.000 claims description 2
239000002184 metal Substances 0.000 claims description 2
125000000732 arylene group Chemical group 0.000 claims 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
150000001875 compounds Chemical class 0.000 description 16
238000000465 moulding Methods 0.000 description 11
XQRLCLUYWUNEEH-UHFFFAOYSA-N diphosphonic acid Chemical class OP(=O)OP(O)=O XQRLCLUYWUNEEH-UHFFFAOYSA-N 0.000 description 5
239000004698 Polyethylene Substances 0.000 description 4
239000000203 mixture Substances 0.000 description 4
239000002530 phenolic antioxidant Substances 0.000 description 4
229920000573 polyethylene Polymers 0.000 description 4
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 3
239000008116 calcium stearate Substances 0.000 description 3
235000013539 calcium stearate Nutrition 0.000 description 3
230000000694 effects Effects 0.000 description 3
230000000087 stabilizing effect Effects 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 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
239000000654 additive Substances 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
230000008033 biological extinction Effects 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
229910000041 hydrogen chloride Inorganic materials 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
238000002156 mixing Methods 0.000 description 2
150000002816 nickel compounds Chemical class 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
238000003756 stirring Methods 0.000 description 2
WWNBZGLDODTKEM-UHFFFAOYSA-N sulfanylidenenickel Chemical compound [Ni]=S WWNBZGLDODTKEM-UHFFFAOYSA-N 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
229910052724 xenon Inorganic materials 0.000 description 2
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 2
GAYUSSOCODCSNF-UHFFFAOYSA-N 1-(dodecyldisulfanyl)dodecane Chemical compound CCCCCCCCCCCCSSCCCCCCCCCCCC GAYUSSOCODCSNF-UHFFFAOYSA-N 0.000 description 1
MQQKTNDBASEZSD-UHFFFAOYSA-N 1-(octadecyldisulfanyl)octadecane Chemical compound CCCCCCCCCCCCCCCCCCSSCCCCCCCCCCCCCCCCCC MQQKTNDBASEZSD-UHFFFAOYSA-N 0.000 description 1
AROCLDYPZXMJPW-UHFFFAOYSA-N 1-(octyldisulfanyl)octane Chemical compound CCCCCCCCSSCCCCCCCC AROCLDYPZXMJPW-UHFFFAOYSA-N 0.000 description 1
IHWDIGHWDQPQMQ-UHFFFAOYSA-N 1-octadecylsulfanyloctadecane Chemical compound CCCCCCCCCCCCCCCCCCSCCCCCCCCCCCCCCCCCC IHWDIGHWDQPQMQ-UHFFFAOYSA-N 0.000 description 1
GEHIXSKXGCIKJJ-UHFFFAOYSA-N 2-(chloromethyl)-5-(4-methoxyphenyl)-1,3,4-oxadiazole Chemical compound C1=CC(OC)=CC=C1C1=NN=C(CCl)O1 GEHIXSKXGCIKJJ-UHFFFAOYSA-N 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
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical class [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
239000003490 Thiodipropionic acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
239000012965 benzophenone Substances 0.000 description 1
150000008366 benzophenones Chemical class 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
UOQACRNTVQWTFF-UHFFFAOYSA-N decane-1,10-dithiol Chemical compound SCCCCCCCCCCS UOQACRNTVQWTFF-UHFFFAOYSA-N 0.000 description 1
LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical class C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
239000003365 glass fiber Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
238000005469 granulation Methods 0.000 description 1
230000003179 granulation Effects 0.000 description 1
239000012760 heat stabilizer Substances 0.000 description 1
238000005286 illumination Methods 0.000 description 1
238000001746 injection moulding Methods 0.000 description 1
QTBFPMKWQKYFLR-UHFFFAOYSA-N isobutyl chloride Chemical compound CC(C)CCl QTBFPMKWQKYFLR-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
238000004519 manufacturing process Methods 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
238000000034 method Methods 0.000 description 1
ZNGLGLXWTVMUCL-UHFFFAOYSA-N methyl(2-methylpropoxy)phosphinic acid Chemical compound CC(C)COP(C)(O)=O ZNGLGLXWTVMUCL-UHFFFAOYSA-N 0.000 description 1
239000000178 monomer Substances 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
150000002898 organic sulfur compounds Chemical class 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical class O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
150000003009 phosphonic acids Chemical class 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920001748 polybutylene Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002243 precursor Substances 0.000 description 1
238000003825 pressing Methods 0.000 description 1
238000003672 processing method Methods 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
238000007711 solidification Methods 0.000 description 1
230000008023 solidification Effects 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
235000019303 thiodipropionic acid Nutrition 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
238000004383 yellowing Methods 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
239000004711 α-olefin Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5313—Phosphinic compounds, e.g. R2=P(:O)OR'
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5317—Phosphonic compounds, e.g. R—P(:O)(OR')2
- C08K5/5333—Esters of phosphonic acids

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)
Anti-Oxidant Or Stabilizer Compositions (AREA)

NO753010A 1974-09-04 1975-09-02 NO753010L (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19742442390 DE2442390C3 (de)		1974-09-04	Stabilisierte Polyolefinformmassen

Publications (1)

Publication Number	Publication Date
NO753010L true NO753010L (fr)	1976-03-05

Family

ID=5924873

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO753010A NO753010L (fr)	1974-09-04	1975-09-02

Country Status (13)

Country	Link
US (1)	US4024103A (fr)
JP (1)	JPS5152450A (fr)
AU (1)	AU8448875A (fr)
BE (1)	BE833068A (fr)
CS (1)	CS180045B2 (fr)
DD (1)	DD120205A5 (fr)
DK (1)	DK395075A (fr)
FI (1)	FI752468A7 (fr)
FR (1)	FR2283925A1 (fr)
NL (1)	NL7510243A (fr)
NO (1)	NO753010L (fr)
SE (1)	SE7509783L (fr)
ZA (1)	ZA755573B (fr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5379935A (en) *	1976-12-24	1978-07-14	Adeka Argus Chem Co Ltd	Stabilized synthetic resin composition
IT1067350B (it) *	1976-12-31	1985-03-16	Mntefibre Spa	Composizioni polimeriche a base di polimeri olefinici
US4111899A (en) *	1977-07-20	1978-09-05	The Dow Chemical Company	Heat stabilized thermoplastic resins containing compounds with phosphorus to phosphorus bonds
EP0003058B1 (fr) *	1978-01-09	1983-02-16	Ciba-Geigy Ag	Polypropylène stabilisé
FR2512039B1 (fr) *	1981-08-26	1985-10-11	Ato Chimie	Composition de resine synthetique ayant une bonne resistance au feu renfermant un polycarbonate, un additif ignifugeant phosphore, et eventuellement d'autres additifs et/ou des charges et objets conformes
US4747966A (en) *	1984-03-30	1988-05-31	Lion Corporation	Electrically conductive thermoplastic resin and coating compositions
US6299983B1 (en)	1997-06-27	2001-10-09	E. I. Du Pont De Nemours And Company	Derivatized metallic surfaces, composites of functionalized polymers with such metallic surfaces and processes for formation thereof
CA2348544A1 (fr) *	1998-11-16	2000-05-25	E.I. Du Pont De Nemours And Company	Surfaces metalliques derivatisees, composites de polymeres fonctionnalises dotes desdites surfaces metalliques et procede de formation desdites surfaces
US7579396B2 (en) *	2007-01-31	2009-08-25	Eastman Kodak Company	Polymer composite
CN103122062A (zh) *	2008-04-03	2013-05-29	巴斯夫欧洲公司	用于聚酯的固相聚合方法的次膦酸化合物

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2230371A (en) *	1939-11-04	1941-02-04	Du Pont	Stabilization of organic substances
US2635112A (en) *	1949-07-28	1953-04-14	Research Corp	Process for producing aminomethylphosphonic acid compounds
US3471552A (en) *	1965-08-24	1969-10-07	Plains Chem Dev Co	Aliphatic polyphosphonic acids and derivatives thereof
US3493538A (en) *	1966-11-30	1970-02-03	Monsanto Co	Discoloration inhibitors for polyethylene
NL7105909A (fr) *	1970-05-04	1971-11-08
US3954847A (en) *	1970-10-22	1976-05-04	Sandoz Ltd.	New benzene phosphonous acid compounds, their production and use as stabilizers for organic materials
DE2252210A1 (de) *	1972-10-25	1974-05-09	Hoechst Ag	Schwerentflammbare thermoplastische polyester

1975
- 1975-08-29 NL NL7510243A patent/NL7510243A/xx unknown
- 1975-09-02 CS CS7500005958A patent/CS180045B2/cs unknown
- 1975-09-02 ZA ZA00755573A patent/ZA755573B/xx unknown
- 1975-09-02 NO NO753010A patent/NO753010L/no unknown
- 1975-09-02 FI FI752468A patent/FI752468A7/fi not_active Application Discontinuation
- 1975-09-02 US US05/609,675 patent/US4024103A/en not_active Expired - Lifetime
- 1975-09-02 DD DD188136A patent/DD120205A5/xx unknown
- 1975-09-03 JP JP50106095A patent/JPS5152450A/ja active Pending
- 1975-09-03 AU AU84488/75A patent/AU8448875A/en not_active Expired
- 1975-09-03 DK DK395075A patent/DK395075A/da unknown
- 1975-09-03 SE SE7509783A patent/SE7509783L/xx unknown
- 1975-09-04 FR FR7527086A patent/FR2283925A1/fr not_active Withdrawn
- 1975-09-04 BE BE159739A patent/BE833068A/fr unknown

Also Published As

Publication number	Publication date
DD120205A5 (fr)	1976-06-05
FI752468A7 (fr)	1976-03-05
DK395075A (da)	1976-03-05
ZA755573B (en)	1976-08-25
FR2283925A1 (fr)	1976-04-02
DE2442390B2 (de)	1977-06-16
BE833068A (fr)	1976-03-04
JPS5152450A (fr)	1976-05-10
NL7510243A (nl)	1976-03-08
US4024103A (en)	1977-05-17
SE7509783L (sv)	1976-03-05
CS180045B2 (en)	1977-12-30
AU8448875A (en)	1977-03-10
DE2442390A1 (de)	1976-04-01

Publication	Publication Date	Title
EP0315162B1 (fr)	1993-04-07	Compositions d'oléfine de grande transparence et résistantes à l'oxydation
US3734885A (en)	1973-05-22	Stabilising homo-or copolymeric polyolefins with diacyl dihydrazides
EP0181023B1 (fr)	1990-03-14	Composés stabilisants pour polymères et compositions polymères stabilisées les contenant
AU732467B2 (en)	2001-04-26	Combination of an organothio compound and a zinc mercapto ester as heat stabilizer in PVC processing
US4024103A (en)	1977-05-17	Stabilized polyolefin molding composition
GB2042512A (en)	1980-09-24	Monoester, compound of 2,2'-alkylidene bis (4,6-di-substituted phenol)
US3772354A (en)	1973-11-13	Stabilizers and polyolefin compositions containing same
NO772119L (no)	1978-01-17	Pigmentert polymersammensetning.
US4952624A (en)	1990-08-28	Polyarylene sulfide mixtures with reduced radical formation under highly accelerated weathering
JP2009522252A (ja)	2009-06-11	カルボキシエチルホスフィネートエステルの塩、及びこれを含む難燃性熱可塑性樹脂組成物
US3479408A (en)	1969-11-18	Beta,beta'-thiodiethyl sulfones
US3676449A (en)	1972-07-11	1,3,4-thiadiazole-bridged thiomethylenephenol antioxidants
US4005094A (en)	1977-01-25	Piperidine-spiro-hydantoin derivatives
US4772651A (en)	1988-09-20	Polyol carboxyalkylthioalkanoesterphenol compounds and organic materials stabilized therewith
US3887516A (en)	1975-06-03	Hindered tris (meta-hydroxybenzylthio)-s-triazine antioxidants
US3296193A (en)	1967-01-03	Stabilized polyolefin compositions containing tin phosphinates
US3637863A (en)	1972-01-25	3 5-di-t-butyl-4-hydroxybenzyl phenyl sulfides
US3644279A (en)	1972-02-22	Polymers of mono-1-olefins stabilized against degradation by ultraviolet light
DE2442390C3 (de)	1978-02-02	Stabilisierte Polyolefinformmassen
US4892930A (en)	1990-01-09	Method for lowering the melt crystallization temperature of an arylene sulfide polymer with organic phosphite composition
JPS6138214B2 (fr)	1986-08-28
US4448915A (en)	1984-05-15	Acetylene carbamide derivatives, processes for their production, and antioxidants for organic substances which comprise such derivatives as active ingredients
US3784510A (en)	1974-01-08	Nickel pyrolyzate stabilizers for olefin polymers
US4220572A (en)	1980-09-02	Polyvinylidene fluoride compositions of improved thermal stability
US3884912A (en)	1975-05-20	4-Piperidone derivatives, their preparation and their use as stabilizers