GB376752A - Improvements in or relating to anti-oxidants for the treatment of rubber - Google Patents
Improvements in or relating to anti-oxidants for the treatment of rubberInfo
- Publication number
- GB376752A GB376752A GB10884/31A GB1088431A GB376752A GB 376752 A GB376752 A GB 376752A GB 10884/31 A GB10884/31 A GB 10884/31A GB 1088431 A GB1088431 A GB 1088431A GB 376752 A GB376752 A GB 376752A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aminodiphenyl
- naphthol
- rubber
- reaction products
- hydroxy compound
- 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)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Antioxidants for rubber are manufactured by condensing together an aminodiphenyl with an aromatic hydroxy compound, preferably a mono-hydroxy compound, with elimination of water. In an example, equimolecular proportions of p-aminodiphenyl and b -naphthol are heated together for 3 to 5 hours at 180-200 DEG C. In another example, p-aminodiphenyl and a slight excess over one molecular proportion of a -naphthol are heated for 3 to 4 hours at 200-240 DEG C. Tables show the antioxidant action of the products on rubber stocks vulcanized with the aid of diphenylguanidine as accelerator. Also specified are the reaction products of p-aminodiphenyl with phenol and with b -b -dioxydinaphthylmethane, and of o-amino-diphenyl with a -naphthol. Reference has been directed by the Comptroller to Specification 352,781.ALSO:As antioxidants for rubber are employed the products obtained by condensing an aminodiphenyl with an aromatic hydroxy compound, perferably a monohydroxy compound, with elimination of water. Tables show the action, on rubber stocks vulcanized with the aid of diphenylguanidine as accelerator, of the reaction products of p-aminodiphenyl with substantially one molecular proportion of b -naphthol and with a slight excess over one molecular proportion of a -naphthol. Also specified are the reaction products of p-aminodiphenyl with phenol and with b -b -dioxydinaphthylmethane, and of o-aminodiphenyl with a -naphthol. Reference has been directed by the Comptroller to Specification 352,781.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US376752XA | 1930-04-15 | 1930-04-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB376752A true GB376752A (en) | 1932-07-13 |
Family
ID=21895670
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB10884/31A Expired GB376752A (en) | 1930-04-15 | 1931-04-13 | Improvements in or relating to anti-oxidants for the treatment of rubber |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB376752A (en) |
-
1931
- 1931-04-13 GB GB10884/31A patent/GB376752A/en not_active Expired
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