DE1142439B - Ungiftige, gegen thermische Oxydation bestaendige Polyaethylenformmassen - Google Patents
Ungiftige, gegen thermische Oxydation bestaendige PolyaethylenformmassenInfo
- Publication number
- DE1142439B DE1142439B DED23639A DED0023639A DE1142439B DE 1142439 B DE1142439 B DE 1142439B DE D23639 A DED23639 A DE D23639A DE D0023639 A DED0023639 A DE D0023639A DE 1142439 B DE1142439 B DE 1142439B
- Authority
- DE
- Germany
- Prior art keywords
- polyethylene
- bis
- thermal oxidation
- toxic
- molding compounds
- 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
- 239000004698 Polyethylene Substances 0.000 title claims description 28
- -1 polyethylene Polymers 0.000 title claims description 28
- 229920000573 polyethylene Polymers 0.000 title claims description 28
- 231100000252 nontoxic Toxicity 0.000 title claims description 9
- 230000003000 nontoxic effect Effects 0.000 title claims description 9
- 230000003647 oxidation Effects 0.000 title claims description 9
- 238000007254 oxidation reaction Methods 0.000 title claims description 9
- 150000001875 compounds Chemical class 0.000 title claims description 8
- 238000000465 moulding Methods 0.000 title claims description 6
- 239000000203 mixture Substances 0.000 claims description 13
- HCZKYJDFEPMADG-UHFFFAOYSA-N nordihydroguaiaretic acid Chemical compound C=1C=C(O)C(O)=CC=1CC(C)C(C)CC1=CC=C(O)C(O)=C1 HCZKYJDFEPMADG-UHFFFAOYSA-N 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 16
- 239000003963 antioxidant agent Substances 0.000 description 10
- 230000006641 stabilisation Effects 0.000 description 9
- 238000011105 stabilization Methods 0.000 description 9
- 239000000473 propyl gallate Substances 0.000 description 8
- 229940075579 propyl gallate Drugs 0.000 description 8
- 235000010388 propyl gallate Nutrition 0.000 description 8
- YMTYZTXUZLQUSF-UHFFFAOYSA-N 3,3'-Dimethylbisphenol A Chemical compound C1=C(O)C(C)=CC(C(C)(C)C=2C=C(C)C(O)=CC=2)=C1 YMTYZTXUZLQUSF-UHFFFAOYSA-N 0.000 description 6
- IJWIRZQYWANBMP-UHFFFAOYSA-N 4-[2-(4-hydroxy-3-propan-2-ylphenyl)propan-2-yl]-2-propan-2-ylphenol Chemical compound C1=C(O)C(C(C)C)=CC(C(C)(C)C=2C=C(C(O)=CC=2)C(C)C)=C1 IJWIRZQYWANBMP-UHFFFAOYSA-N 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 5
- 230000003078 antioxidant effect Effects 0.000 description 4
- 235000013305 food Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- ZDRSNHRWLQQICP-UHFFFAOYSA-N 2-tert-butyl-4-[2-(3-tert-butyl-4-hydroxyphenyl)propan-2-yl]phenol Chemical compound C1=C(O)C(C(C)(C)C)=CC(C(C)(C)C=2C=C(C(O)=CC=2)C(C)(C)C)=C1 ZDRSNHRWLQQICP-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 230000036284 oxygen consumption Effects 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 239000003440 toxic substance Substances 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- ZROJGLDKQRJURL-UHFFFAOYSA-N 1-methyl-2-[2-(2-methylphenyl)propan-2-yl]benzene Chemical compound CC1=CC=CC=C1C(C)(C)C1=CC=CC=C1C ZROJGLDKQRJURL-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- XCUMMFDPFFDQEX-UHFFFAOYSA-N 2-butan-2-yl-4-[2-(3-butan-2-yl-4-hydroxyphenyl)propan-2-yl]phenol Chemical compound C1=C(O)C(C(C)CC)=CC(C(C)(C)C=2C=C(C(O)=CC=2)C(C)CC)=C1 XCUMMFDPFFDQEX-UHFFFAOYSA-N 0.000 description 1
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 1
- SVOBELCYOCEECO-UHFFFAOYSA-N 4-[1-(4-hydroxy-3-methylphenyl)cyclohexyl]-2-methylphenol Chemical compound C1=C(O)C(C)=CC(C2(CCCCC2)C=2C=C(C)C(O)=CC=2)=C1 SVOBELCYOCEECO-UHFFFAOYSA-N 0.000 description 1
- OBTLOFBIJUUMGC-UHFFFAOYSA-N 4-[1-(4-hydroxy-3-propan-2-ylphenyl)butyl]-2-propan-2-ylphenol Chemical compound C=1C=C(O)C(C(C)C)=CC=1C(CCC)C1=CC=C(O)C(C(C)C)=C1 OBTLOFBIJUUMGC-UHFFFAOYSA-N 0.000 description 1
- CSNLMVVOOYVWSX-UHFFFAOYSA-N 4-[1-(4-hydroxy-3-propan-2-ylphenyl)cyclohexyl]-2-propan-2-ylphenol Chemical compound C1=C(O)C(C(C)C)=CC(C2(CCCCC2)C=2C=C(C(O)=CC=2)C(C)C)=C1 CSNLMVVOOYVWSX-UHFFFAOYSA-N 0.000 description 1
- OTMOITAVSCHTET-UHFFFAOYSA-N 4-[1-(4-hydroxy-3-propan-2-ylphenyl)propyl]-2-propan-2-ylphenol Chemical compound C=1C=C(O)C(C(C)C)=CC=1C(CC)C1=CC=C(O)C(C(C)C)=C1 OTMOITAVSCHTET-UHFFFAOYSA-N 0.000 description 1
- WXAWSIXTNRKGGJ-UHFFFAOYSA-N 4-[2-(4-hydroxy-3-propan-2-ylphenyl)butan-2-yl]-2-propan-2-ylphenol Chemical compound C=1C=C(O)C(C(C)C)=CC=1C(C)(CC)C1=CC=C(O)C(C(C)C)=C1 WXAWSIXTNRKGGJ-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 229940078552 o-xylene Drugs 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000010186 staining Methods 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
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
-
- 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
- C08K5/13—Phenols; Phenolates
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 |
|---|---|---|---|
| US356276XA | 1955-09-22 | 1955-09-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1142439B true DE1142439B (de) | 1963-01-17 |
Family
ID=21883836
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DED23639A Pending DE1142439B (de) | 1955-09-22 | 1956-08-21 | Ungiftige, gegen thermische Oxydation bestaendige Polyaethylenformmassen |
Country Status (6)
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE571035A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1957-09-07 | |||
| DE1191567B (de) * | 1958-09-18 | 1965-04-22 | Du Pont | Formmassen aus Propylenpolymerisaten und einer Stabilisatorkombination |
| DE1171607B (de) * | 1960-01-04 | 1964-06-04 | Eastman Kodak Co | Formmassen aus Polyolefinen |
| NL126688C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1960-08-29 |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB585504A (en) * | 1944-02-05 | 1947-02-07 | Du Pont | Improvements in or relating to polythene compositions |
| US2434662A (en) * | 1944-02-03 | 1948-01-20 | Du Pont | Polyethylene stabilized with bis-(hydroxyphenyl) propanes |
| US2435245A (en) * | 1944-02-05 | 1948-02-03 | Du Pont | Stabilized polymers of ethylene |
| US2448799A (en) * | 1945-11-03 | 1948-09-07 | Du Pont | Ethylene polymer compositions |
| GB618839A (en) * | 1945-11-15 | 1949-02-28 | Du Pont | Improvements in or relating to polymers of ethylene |
| US2591651A (en) * | 1949-11-21 | 1952-04-01 | Standard Oil Dev Co | Stabilized organic compositions containing bis (hydroxy alkoxy phenyl) alkanes |
| GB722873A (en) * | 1951-12-17 | 1955-02-02 | Bataafsche Petroleum | Oleaginous compositions |
-
0
- NL NL98793D patent/NL98793C/xx active
- BE BE550337D patent/BE550337A/xx unknown
- NL NL209512D patent/NL209512A/xx unknown
-
1956
- 1956-07-30 GB GB23505/56A patent/GB793430A/en not_active Expired
- 1956-08-07 FR FR1155679D patent/FR1155679A/fr not_active Expired
- 1956-08-21 DE DED23639A patent/DE1142439B/de active Pending
- 1956-09-11 CH CH356276D patent/CH356276A/de unknown
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2434662A (en) * | 1944-02-03 | 1948-01-20 | Du Pont | Polyethylene stabilized with bis-(hydroxyphenyl) propanes |
| GB585504A (en) * | 1944-02-05 | 1947-02-07 | Du Pont | Improvements in or relating to polythene compositions |
| US2435245A (en) * | 1944-02-05 | 1948-02-03 | Du Pont | Stabilized polymers of ethylene |
| US2448799A (en) * | 1945-11-03 | 1948-09-07 | Du Pont | Ethylene polymer compositions |
| GB618839A (en) * | 1945-11-15 | 1949-02-28 | Du Pont | Improvements in or relating to polymers of ethylene |
| US2591651A (en) * | 1949-11-21 | 1952-04-01 | Standard Oil Dev Co | Stabilized organic compositions containing bis (hydroxy alkoxy phenyl) alkanes |
| GB722873A (en) * | 1951-12-17 | 1955-02-02 | Bataafsche Petroleum | Oleaginous compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| GB793430A (en) | 1958-04-16 |
| BE550337A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| NL209512A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| CH356276A (de) | 1961-08-15 |
| NL98793C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| FR1155679A (fr) | 1958-05-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1271389B (de) | Stabilisieren halogenhaltiger Polymerisate | |
| DE1142439B (de) | Ungiftige, gegen thermische Oxydation bestaendige Polyaethylenformmassen | |
| AT389816B (de) | Verfahren zur herstellung eines elixiers auf basis von wachteleiern | |
| DE1542730A1 (de) | Schaedlingsbekaempfungsmittel mit verlaengerter Wirksamkeit | |
| DE1519103A1 (de) | N,N-dialkylierte Hydroxylamine als Hautverhuetungsmittel | |
| EP0076471B1 (de) | Stabilisieren von Polyether- oder Polyester-Formmassen gegen vorzeitige Reaktion | |
| DE2308225A1 (de) | Pvc-mischung | |
| EP0194466A2 (de) | Kombination zur antimikrobiellen und antioxidativen Stabilisierung von Externa und Körperpflegemitteln | |
| DE1232742B (de) | Formmassen aus Olefinpolymerisaten | |
| DE1262512B (de) | Stabilisierte germicide Massen auf der Basis von Halogensalicylaniliden | |
| DE2420968A1 (de) | Mit alkylierten phenolen stabilisierte acrylsaeure | |
| DE812248C (de) | Verfahren zur Herstellung von stabilem Perborat | |
| DE1062857B (de) | Verfahren zum Stabilisieren von Fetten, OElen, Wachsen und Kohlenwasserstoffen gegen Oxydation | |
| DE1172042B (de) | Verfahren zum Stabilisieren von Homo- oder Mischpolymerisaten von ª-Mono-olefinen | |
| DE1206150B (de) | Ozonschutzmittel fuer Kautschuk | |
| DE828842C (de) | Verfahren zur Verhinderung bzw. Verzoegerung der Autoxydation cyclischer AEther | |
| AT248108B (de) | Stabilisierte Polymere oder Copolymere von äthylenisch ungesättigten Kohlenwasserstoffen | |
| AT334884B (de) | Verfahren zur herstellung von neuen phenyl-benzyl-ketonen | |
| DE1275327B (de) | Stabilisiertes insektizides und akarizides Mittel | |
| DE1719245C3 (de) | Ozonschutzmittelgemische für natürliche und synthetische vulkanisierbare Kautschuke | |
| AT134262B (de) | Natriumhydrosulfit-Präparate. | |
| DE1941691B2 (de) | Ozonschutzmittel für Kautschuk | |
| DE1126134B (de) | Verfahren zum Stabilisieren von Polyaethern durch Phenole gegen Oxydation | |
| DE368490C (de) | Verfahren zum Impraegnieren von Holz | |
| DE1053734B (de) | Verfahren zur Loeslichmachung und Stabilisierung der Tetracyclinantibiotika |