NO121470B - - Google Patents
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- Publication number
- NO121470B NO121470B NO165995A NO16599566A NO121470B NO 121470 B NO121470 B NO 121470B NO 165995 A NO165995 A NO 165995A NO 16599566 A NO16599566 A NO 16599566A NO 121470 B NO121470 B NO 121470B
- Authority
- NO
- Norway
- Prior art keywords
- hydroxy
- carbon atoms
- group
- benzo
- stabilizer
- Prior art date
Links
- 239000003381 stabilizer Substances 0.000 claims description 18
- 229920000098 polyolefin Polymers 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 150000002736 metal compounds Chemical class 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 150000002902 organometallic compounds Chemical class 0.000 claims 1
- 230000002195 synergetic effect Effects 0.000 claims 1
- -1 phenols Chemical class 0.000 description 11
- 150000001463 antimony compounds Chemical class 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 5
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229920001155 polypropylene Polymers 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- 235000013824 polyphenols Nutrition 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000005083 Zinc sulfide Substances 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 150000008442 polyphenolic compounds Chemical class 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 2
- MQQKTNDBASEZSD-UHFFFAOYSA-N 1-(octadecyldisulfanyl)octadecane Chemical compound CCCCCCCCCCCCCCCCCCSSCCCCCCCCCCCCCCCCCC MQQKTNDBASEZSD-UHFFFAOYSA-N 0.000 description 1
- PBCMRNUMIAQRBZ-UHFFFAOYSA-N 1-(octadecyltetrasulfanyl)octadecane Chemical compound CCCCCCCCCCCCCCCCCCSSSSCCCCCCCCCCCCCCCCCC PBCMRNUMIAQRBZ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- VZWGRQBCURJOMT-UHFFFAOYSA-N acetic acid n-dodecyl ester Natural products CCCCCCCCCCCCOC(C)=O VZWGRQBCURJOMT-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- LNTHITQWFMADLM-UHFFFAOYSA-N anhydrous gallic acid Natural products OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- WBTCZEPSIIFINA-MSFWTACDSA-J dipotassium;antimony(3+);(2r,3r)-2,3-dioxidobutanedioate;trihydrate Chemical compound O.O.O.[K+].[K+].[Sb+3].[Sb+3].[O-]C(=O)[C@H]([O-])[C@@H]([O-])C([O-])=O.[O-]C(=O)[C@H]([O-])[C@@H]([O-])C([O-])=O WBTCZEPSIIFINA-MSFWTACDSA-J 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052976 metal sulfide Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- YTXCAJNHPVBVDJ-UHFFFAOYSA-N octadecyl propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CC YTXCAJNHPVBVDJ-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 150000003464 sulfur compounds Chemical class 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
- C08K5/372—Sulfides, e.g. R-(S)x-R'
-
- 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
- C08K5/59—Arsenic- or antimony-containing compounds
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF47977A DE1265986B (de) | 1965-12-21 | 1965-12-21 | Verfahren zum Stabilisieren von Polymerisaten von Olefinen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO121470B true NO121470B (enExample) | 1971-03-01 |
Family
ID=7101952
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO165995A NO121470B (enExample) | 1965-12-21 | 1966-12-14 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US3459705A (enExample) |
| AT (1) | AT266438B (enExample) |
| BE (1) | BE691547A (enExample) |
| CH (1) | CH479643A (enExample) |
| DE (1) | DE1265986B (enExample) |
| DK (1) | DK114795B (enExample) |
| ES (1) | ES334706A1 (enExample) |
| FR (1) | FR1505926A (enExample) |
| GB (1) | GB1162259A (enExample) |
| NL (1) | NL6616510A (enExample) |
| NO (1) | NO121470B (enExample) |
| SE (1) | SE309674B (enExample) |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2488975A (en) * | 1947-01-16 | 1949-11-22 | Us Rubber Co | Antimonyl derivatives of polyhydric phenols as antioxidants |
| US2581909A (en) * | 1949-03-30 | 1952-01-08 | Firestone Tire & Rubber Co | Stabilization of acrylonitrile-butadiene-1, 3 copolymers |
| US2581910A (en) * | 1949-03-30 | 1952-01-08 | Firestone Tire & Rubber Co | Acrylonitrile-butadiene-1, 3 copolymers stabilized by antimonyl p-phenyl catecholate |
| US2581911A (en) * | 1949-03-30 | 1952-01-08 | Firestone Tire & Rubber Co | Acrylonitrile-butadiene-1, 3 copolymers stabilized by antimonyl pyrogallolate |
| US2686167A (en) * | 1952-09-10 | 1954-08-10 | Firestone Tire & Rubber Co | Stabilization of synthetic rubbers with a sulfite and an antimonyl compound |
| US3255136A (en) * | 1960-05-27 | 1966-06-07 | Argus Chem | Stabilization of polypropylene with mixtures comprising organic-phosphite phenol transesterification products and esters of thiodipropionic acid |
-
1965
- 1965-12-21 DE DEF47977A patent/DE1265986B/de active Pending
-
1966
- 1966-11-23 NL NL6616510A patent/NL6616510A/xx unknown
- 1966-12-08 DK DK637566AA patent/DK114795B/da unknown
- 1966-12-13 GB GB55829/66A patent/GB1162259A/en not_active Expired
- 1966-12-14 AT AT1151466A patent/AT266438B/de active
- 1966-12-14 NO NO165995A patent/NO121470B/no unknown
- 1966-12-16 CH CH1800466A patent/CH479643A/de not_active IP Right Cessation
- 1966-12-16 US US602169A patent/US3459705A/en not_active Expired - Lifetime
- 1966-12-20 SE SE17451/66A patent/SE309674B/xx unknown
- 1966-12-20 ES ES334706A patent/ES334706A1/es not_active Expired
- 1966-12-21 FR FR88367A patent/FR1505926A/fr not_active Expired
- 1966-12-21 BE BE691547D patent/BE691547A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL6616510A (enExample) | 1967-06-22 |
| BE691547A (enExample) | 1967-06-21 |
| AT266438B (de) | 1968-11-11 |
| GB1162259A (en) | 1969-08-20 |
| DK114795B (da) | 1969-08-04 |
| CH479643A (de) | 1969-10-15 |
| SE309674B (enExample) | 1969-03-31 |
| US3459705A (en) | 1969-08-05 |
| FR1505926A (fr) | 1967-12-15 |
| DE1265986B (de) | 1968-04-11 |
| ES334706A1 (es) | 1968-06-01 |
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