DE1219222B - Formmassen aus kristallinen Polyolefinen - Google Patents
Formmassen aus kristallinen PolyolefinenInfo
- Publication number
- DE1219222B DE1219222B DEM55046A DEM0055046A DE1219222B DE 1219222 B DE1219222 B DE 1219222B DE M55046 A DEM55046 A DE M55046A DE M0055046 A DEM0055046 A DE M0055046A DE 1219222 B DE1219222 B DE 1219222B
- Authority
- DE
- Germany
- Prior art keywords
- thio
- bis
- crystalline polyolefins
- molding compounds
- hours
- 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.)
- Pending
Links
- 229920000098 polyolefin Polymers 0.000 title claims description 11
- 150000001875 compounds Chemical class 0.000 title claims description 6
- 238000000465 moulding Methods 0.000 title claims description 5
- 239000000203 mixture Substances 0.000 claims description 21
- 239000003381 stabilizer Substances 0.000 claims description 13
- 150000007970 thio esters Chemical class 0.000 claims description 6
- 235000021355 Stearic acid Nutrition 0.000 claims description 4
- 229910017053 inorganic salt Inorganic materials 0.000 claims description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 4
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 4
- 239000008117 stearic acid Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- -1 Polypropylene Polymers 0.000 description 7
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 6
- 229920001155 polypropylene Polymers 0.000 description 6
- HXIQYSLFEXIOAV-UHFFFAOYSA-N 2-tert-butyl-4-(5-tert-butyl-4-hydroxy-2-methylphenyl)sulfanyl-5-methylphenol Chemical compound CC1=CC(O)=C(C(C)(C)C)C=C1SC1=CC(C(C)(C)C)=C(O)C=C1C HXIQYSLFEXIOAV-UHFFFAOYSA-N 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 4
- 239000008116 calcium stearate Substances 0.000 description 4
- 235000013539 calcium stearate Nutrition 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 238000009987 spinning Methods 0.000 description 4
- 230000000087 stabilizing effect Effects 0.000 description 4
- 238000003878 thermal aging Methods 0.000 description 4
- 238000000605 extraction Methods 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- 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 description 1
- ODJQKYXPKWQWNK-UHFFFAOYSA-N 3,3'-Thiobispropanoic acid Chemical class OC(=O)CCSCCC(O)=O ODJQKYXPKWQWNK-UHFFFAOYSA-N 0.000 description 1
- ZVZCJDNOAPBPMI-UHFFFAOYSA-N CCCCCCCCCCCCOC(=S)COCC(O)=O Chemical compound CCCCCCCCCCCCOC(=S)COCC(O)=O ZVZCJDNOAPBPMI-UHFFFAOYSA-N 0.000 description 1
- GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 description 1
- 239000003508 Dilauryl thiodipropionate Substances 0.000 description 1
- 206010068188 Heat illness Diseases 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 235000019304 dilauryl thiodipropionate Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- GSVIFLAGXMBTDQ-UHFFFAOYSA-N dodecyl 2-(2-dodecoxy-2-sulfanylideneethoxy)acetate Chemical compound CCCCCCCCCCCCOC(=O)COCC(=S)OCCCCCCCCCCCC GSVIFLAGXMBTDQ-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals 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'
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)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT2228361 | 1961-12-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1219222B true DE1219222B (de) | 1966-06-16 |
Family
ID=11194133
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEM55046A Pending DE1219222B (de) | 1961-12-11 | 1962-12-07 | Formmassen aus kristallinen Polyolefinen |
Country Status (12)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1544768B2 (de) * | 1964-12-02 | 1970-09-10 | Deutsche Advance Produktion GmbH, 6141 Lautern | Stabilisieren von Vinylchloridpolymerxsaten |
| GB1547331A (en) * | 1976-04-06 | 1979-06-13 | Mitsubishi Petrochemical Co | Method of stabilizing an olefin polymer |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE582162A (US08063081-20111122-C00044.png) * | 1958-09-18 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2965060A (en) * | 1956-07-20 | 1960-12-20 | Asano Uichiro | Structure of submarine boats |
| US3069369A (en) * | 1957-11-14 | 1962-12-18 | Monsanto Chemicals | Color stabilized polyethylene compounds |
| US3222318A (en) * | 1962-09-11 | 1965-12-07 | Nat Distillers Chem Corp | Polypropylene stabilized with dithiotriglycol dilaurate |
| US3226357A (en) * | 1962-09-11 | 1965-12-28 | Nat Distillers Chem Corp | Polyolefins stabilized with derivatives of xylylene thioethers |
-
0
- BE BE625896D patent/BE625896A/xx unknown
- FR FR1342478D patent/FR1342478A/fr not_active Expired
- NL NL286451D patent/NL286451A/xx unknown
-
1962
- 1962-12-07 DE DEM55046A patent/DE1219222B/de active Pending
- 1962-12-07 AT AT960362A patent/AT238449B/de active
- 1962-12-07 US US243708A patent/US3280058A/en not_active Expired - Lifetime
- 1962-12-08 CH CH1441362A patent/CH427254A/de unknown
- 1962-12-08 CA CA864,094A patent/CA944886A/en not_active Expired
- 1962-12-10 GB GB46536/62A patent/GB957395A/en not_active Expired
- 1962-12-10 ES ES283244A patent/ES283244A1/es not_active Expired
- 1962-12-10 NO NO146753A patent/NO122806B/no unknown
- 1962-12-10 FI FI2214/62A patent/FI40228B/fi active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE582162A (US08063081-20111122-C00044.png) * | 1958-09-18 |
Also Published As
| Publication number | Publication date |
|---|---|
| ES283244A1 (es) | 1963-07-01 |
| CH427254A (de) | 1966-12-31 |
| GB957395A (en) | 1964-05-06 |
| NO122806B (US08063081-20111122-C00044.png) | 1971-08-16 |
| US3280058A (en) | 1966-10-18 |
| BE625896A (US08063081-20111122-C00044.png) | |
| AT238449B (de) | 1965-02-10 |
| NL286451A (US08063081-20111122-C00044.png) | |
| CA944886A (en) | 1974-04-02 |
| FR1342478A (US08063081-20111122-C00044.png) | 1964-02-07 |
| FI40228B (US08063081-20111122-C00044.png) | 1968-07-31 |
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