GB570232A - Improvements in anti-oxidants - Google Patents
Improvements in anti-oxidantsInfo
- Publication number
- GB570232A GB570232A GB434/42A GB43442A GB570232A GB 570232 A GB570232 A GB 570232A GB 434/42 A GB434/42 A GB 434/42A GB 43442 A GB43442 A GB 43442A GB 570232 A GB570232 A GB 570232A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxide
- diphenyl
- amine
- diamine
- rubber
- 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
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
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C08K5/18—Amines; Quaternary ammonium compounds with aromatically bound amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Antioxidants for rubber, balata, guttapercha, &c. or synthetic rubber, unsaturated vegetable or other fatty oils, essential oils, petroleum oils and their derivatives, gasoline, soaps, aldehydes, synthetic resins, turpentine or paints, &c., comprise the reaction products of an olefine oxide with an aromatic di-secondary amine. The oxide may be ethylene-, propylene-, butylene-, amylene- or tri-, tetra- or pentamethylene oxide, and the amine may have the formula R1-NH-Ar-NH-R2, where Ar is an arylene group, and R1 and R2 are each aromatic groups such as phenyl, naphthyl, &c. which may include further substituents, e.g. diphenyl, ditolyl-, dianisyl-, dinapthyl, dihydro-phenyl-, or dixylyl phenylene diamine, diphenyl p-tolylene diamine, diphenyl naphthalene diamine diamino-diphenyl. The oxide or vapour may be passed through the amine, or a solution of the reactants in dioxane or benzene may be refluxed, or the reactants may be heated in a sealed tube. A halogen or halogen acid &c. catalyst may be used. If acid, the products may be neutralized with alkali. In an example, 6 c.c. of ethylene oxide were reacted with 26 gms. of N,N1-diphenyl p-phenylene diamine by heating overnight at 175 DEG C. and 1 per cent of the purified product, a thick oil, added to smoked sheet rubber in a mix including carbon black, zinc soap, pine tar, zinc oxide, sulphur and an accelerator.ALSO:Antioxidants for rubber, balata, guttapercha, &c. or synthetic rubber, unsaturated vegetable or other fatty oils, essential oils, petroleum oils and their derivatives gasoline, soaps, aldehydes, synthetic resins, turpentine or paints, &c., comprise the reaction products of an olefine oxide with an aromatic di-secondary amine. The oxide may be ethylene-, propylene-, butylene-, amylene- or tri-, tetra- or pentamethylene oxide, and the amine may have the formula R1-NH-Ar-NH-R2, where Ar is an arylene group, and R1 and R2 are each aromatic groups such as phenyl, naphthyl, &c. which may include further substituents, e.g. diphenyl, ditolyl-, dianisyl-, dinaphthyl-dihydroxy phenyl-, or dixenyl phenylene diamine, diphenyl p-tolylene diamine, diphenyl naphthalene diamine, or dianilino diphenyl. The oxide or vapour may be passed through the amine, or a solution of the reactants in dioxane or benzene may be refluxed, or the reactants may be heated in a sealed tube. A halogen or halogen acid &c. catalyst may be used. If acid, the products may be neutralized with alkali. In an example, 6 c.c. of ethylene oxide were reacted with 26 gms. of N,N1 - diphenyl p-phenylene diamine by heating overnight at 175 DEG C. and 1 per cent of the purified product, a thick oil, added to smoked sheet rubber in a mix including carbon black, zinc soap, pine tar, zinc oxide, sulphur and an accelerator.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US570232XA | 1941-01-15 | 1941-01-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB570232A true GB570232A (en) | 1945-06-28 |
Family
ID=22008016
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB434/42A Expired GB570232A (en) | 1941-01-15 | 1942-01-12 | Improvements in anti-oxidants |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB570232A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1068411B (en) * | 1955-04-14 | 1959-11-05 | Olin Mathieson Chemical Corporation, Baltimore, Md. (V. St. A.) | Stabilized soap |
DE1137731B (en) * | 1958-08-05 | 1962-10-11 | Hoechst Ag | Process for obtaining pure and at the same time stabilized sorbic acid |
WO2010060818A1 (en) * | 2008-11-25 | 2010-06-03 | Basf Se | Alkoxylated oligoamines or polyamines as oxidation stabilizers |
CN115536913A (en) * | 2022-10-12 | 2022-12-30 | 科迈特新材料有限公司 | Heat-resistant and aging-resistant modifier for rubber and preparation method thereof |
-
1942
- 1942-01-12 GB GB434/42A patent/GB570232A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1068411B (en) * | 1955-04-14 | 1959-11-05 | Olin Mathieson Chemical Corporation, Baltimore, Md. (V. St. A.) | Stabilized soap |
DE1137731B (en) * | 1958-08-05 | 1962-10-11 | Hoechst Ag | Process for obtaining pure and at the same time stabilized sorbic acid |
WO2010060818A1 (en) * | 2008-11-25 | 2010-06-03 | Basf Se | Alkoxylated oligoamines or polyamines as oxidation stabilizers |
CN115536913A (en) * | 2022-10-12 | 2022-12-30 | 科迈特新材料有限公司 | Heat-resistant and aging-resistant modifier for rubber and preparation method thereof |
CN115536913B (en) * | 2022-10-12 | 2024-04-16 | 科迈特新材料有限公司 | Heat-resistant and aging-resistant modifier for rubber and preparation method thereof |
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