GB1345542A - Stabilisation of polyolefine products - Google Patents
Stabilisation of polyolefine productsInfo
- Publication number
- GB1345542A GB1345542A GB1282371*[A GB1282371A GB1345542A GB 1345542 A GB1345542 A GB 1345542A GB 1282371 A GB1282371 A GB 1282371A GB 1345542 A GB1345542 A GB 1345542A
- Authority
- GB
- United Kingdom
- Prior art keywords
- nickel
- hydroxy
- tetraethyl
- diethylphosphonobenzyl
- bis
- 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.)
- Expired
Links
- 229920000098 polyolefin Polymers 0.000 title abstract 3
- 230000006641 stabilisation Effects 0.000 title 1
- CJOBVZJTOIVNNF-UHFFFAOYSA-N cadmium sulfide Chemical compound [Cd]=S CJOBVZJTOIVNNF-UHFFFAOYSA-N 0.000 abstract 5
- 229910052980 cadmium sulfide Inorganic materials 0.000 abstract 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 4
- -1 phosphorus compound Chemical class 0.000 abstract 4
- PWBRLMKOCGLZAH-UHFFFAOYSA-N 2-(4-ethylphenyl)acetaldehyde Chemical compound CCC1=CC=C(CC=O)C=C1 PWBRLMKOCGLZAH-UHFFFAOYSA-N 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 abstract 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 239000005864 Sulphur Substances 0.000 abstract 2
- 239000000654 additive Substances 0.000 abstract 2
- 230000000996 additive effect Effects 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- AIPRAPZUGUTQKX-UHFFFAOYSA-N diethoxyphosphorylmethylbenzene Chemical compound CCOP(=O)(OCC)CC1=CC=CC=C1 AIPRAPZUGUTQKX-UHFFFAOYSA-N 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 229910052759 nickel Inorganic materials 0.000 abstract 2
- CLQUXJZJDVHHMG-UHFFFAOYSA-N nickel;phenol Chemical compound [Ni].OC1=CC=CC=C1.OC1=CC=CC=C1 CLQUXJZJDVHHMG-UHFFFAOYSA-N 0.000 abstract 2
- 229910052698 phosphorus Inorganic materials 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- 125000001174 sulfone group Chemical group 0.000 abstract 2
- AUUYGJICJNWARU-UHFFFAOYSA-N tris[diethoxyphosphoryl(phenyl)methyl] phosphite Chemical compound P(OC(C1=CC=CC=C1)P(=O)(OCC)OCC)(OC(C1=CC=CC=C1)P(=O)(OCC)OCC)OC(C1=CC=CC=C1)P(=O)(OCC)OCC AUUYGJICJNWARU-UHFFFAOYSA-N 0.000 abstract 2
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical class OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 abstract 1
- QUHCTSBIJDBBAC-UHFFFAOYSA-N 1,4-bis(diethoxyphosphorylmethyl)-2,5-dimethylbenzene Chemical compound CCOP(=O)(OCC)CC1=CC(C)=C(CP(=O)(OCC)OCC)C=C1C QUHCTSBIJDBBAC-UHFFFAOYSA-N 0.000 abstract 1
- WQYFETFRIRDUPJ-UHFFFAOYSA-N 2-[2-hydroxy-5-(2,4,4-trimethylpentan-2-yl)phenyl]sulfanyl-4-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(O)C(SC=2C(=CC=C(C=2)C(C)(C)CC(C)(C)C)O)=C1 WQYFETFRIRDUPJ-UHFFFAOYSA-N 0.000 abstract 1
- ODJQKYXPKWQWNK-UHFFFAOYSA-L 3-(2-carboxylatoethylsulfanyl)propanoate Chemical compound [O-]C(=O)CCSCCC([O-])=O ODJQKYXPKWQWNK-UHFFFAOYSA-L 0.000 abstract 1
- VWGKEVWFBOUAND-UHFFFAOYSA-N 4,4'-thiodiphenol Chemical compound C1=CC(O)=CC=C1SC1=CC=C(O)C=C1 VWGKEVWFBOUAND-UHFFFAOYSA-N 0.000 abstract 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 abstract 1
- ZCILGMFPJBRCNO-UHFFFAOYSA-N 4-phenyl-2H-benzotriazol-5-ol Chemical class OC1=CC=C2NN=NC2=C1C1=CC=CC=C1 ZCILGMFPJBRCNO-UHFFFAOYSA-N 0.000 abstract 1
- GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000003508 Dilauryl thiodipropionate Substances 0.000 abstract 1
- 239000004743 Polypropylene Substances 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 235000001014 amino acid Nutrition 0.000 abstract 1
- 150000001413 amino acids Chemical class 0.000 abstract 1
- 150000001491 aromatic compounds Chemical class 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- OGBVRMYSNSKIEF-UHFFFAOYSA-L benzyl-dioxido-oxo-$l^{5}-phosphane Chemical compound [O-]P([O-])(=O)CC1=CC=CC=C1 OGBVRMYSNSKIEF-UHFFFAOYSA-L 0.000 abstract 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 235000019304 dilauryl thiodipropionate Nutrition 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 150000002815 nickel Chemical class 0.000 abstract 1
- 150000002816 nickel compounds Chemical class 0.000 abstract 1
- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 150000003009 phosphonic acids Chemical class 0.000 abstract 1
- 239000011574 phosphorus Substances 0.000 abstract 1
- 150000003018 phosphorus compounds Chemical class 0.000 abstract 1
- 229920001155 polypropylene Polymers 0.000 abstract 1
- 229920006216 polyvinyl aromatic Polymers 0.000 abstract 1
- 239000003381 stabilizer Substances 0.000 abstract 1
- 230000000087 stabilizing effect Effects 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 150000003568 thioethers Chemical class 0.000 abstract 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
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)
- Artificial Filaments (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT2414870 | 1970-05-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1345542A true GB1345542A (en) | 1974-01-30 |
Family
ID=11212228
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1282371*[A Expired GB1345542A (en) | 1970-05-04 | 1971-05-03 | Stabilisation of polyolefine products |
Country Status (9)
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3893970A (en) * | 1971-10-01 | 1975-07-08 | Cities Service Co | Fire retardant polypropylene compositions containing a halogenated flame retardant and a phosphite adjuvant |
| US3975358A (en) * | 1972-04-26 | 1976-08-17 | American Cyanamid Company | Polymers stabilized with an organo-nickel compound and a dialkyl pentaerythritol diphosphite |
| US4199494A (en) * | 1973-09-13 | 1980-04-22 | Ciba-Geigy Corporation | Metal complexes of α-aminophosphonic acid half-esters and of α-a |
| US4148747A (en) * | 1973-10-11 | 1979-04-10 | Raychem Corporation | Antioxidant comprising a hydroxy aromatic compound containing sulfur and an organic phosphonate |
| NL7510243A (nl) * | 1974-09-04 | 1976-03-08 | Hoechst Ag | Gestabiliseerde polyalkeenvormmassa. |
| JPS5379935A (en) * | 1976-12-24 | 1978-07-14 | Adeka Argus Chem Co Ltd | Stabilized synthetic resin composition |
| US4144029A (en) * | 1977-07-29 | 1979-03-13 | American Cyanamid Company | Nickel stabilizers and dye enhancers for polyolefins |
-
1971
- 1971-04-29 NL NL7105909A patent/NL7105909A/xx not_active Application Discontinuation
- 1971-05-03 FR FR7115830A patent/FR2091104A5/fr not_active Expired
- 1971-05-03 BE BE766607A patent/BE766607A/xx unknown
- 1971-05-03 AT AT379671A patent/AT312299B/de not_active IP Right Cessation
- 1971-05-03 ES ES390825A patent/ES390825A1/es not_active Expired
- 1971-05-03 CA CA111,988A patent/CA961592A/en not_active Expired
- 1971-05-03 US US00139919A patent/US3749694A/en not_active Expired - Lifetime
- 1971-05-03 GB GB1282371*[A patent/GB1345542A/en not_active Expired
- 1971-05-04 DE DE19712122069 patent/DE2122069A1/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CA961592A (en) | 1975-01-21 |
| NL7105909A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1971-11-08 |
| DE2122069A1 (de) | 1971-11-18 |
| FR2091104A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1972-01-14 |
| ES390825A1 (es) | 1974-10-01 |
| US3749694A (en) | 1973-07-31 |
| AT312299B (de) | 1973-12-27 |
| BE766607A (fr) | 1971-11-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |