GB488866A - The manufacture of stable synthetic rubber - Google Patents
The manufacture of stable synthetic rubberInfo
- Publication number
- GB488866A GB488866A GB1147/37A GB114737A GB488866A GB 488866 A GB488866 A GB 488866A GB 1147/37 A GB1147/37 A GB 1147/37A GB 114737 A GB114737 A GB 114737A GB 488866 A GB488866 A GB 488866A
- Authority
- GB
- United Kingdom
- Prior art keywords
- parts
- butadiene
- stabilizer
- sulphur
- latex
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
- C08K5/375—Thiols containing six-membered aromatic rings
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)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Synthetic rubber-like materials such as polymers of butadiene, isoprene, dimethyl butadiene, 2-chlorbutadiene, and joint polymers of these substances with other polymerizable substances, such as styrene and acrylic nitrile, are stabilized by adding sulphides or polysulphides of alkylated phenols such as may be prepared by reacting an alkylated phenol with sulphur chloride or monochloride or by melting the alkylated phenol with sulphur. The stabilizer may be added to the solid polymer on the roller or to the synthetic latex where emulsion polymerization is employed. Examples describe (1) and (2) the addition of di(tertiary amyl phenol) disulphide to a synthetic latex prepared by emulsion polymerization of butadiene with acrylic nitrile and styrene respectively; (4) the addition of cresol sulphide to a latex from butadiene and acrylic nitrile; (5) the addition of diisobutyl sulphide to a latex from 2-chlorbutadiene. Particulars are given of the properties of the various polymers: (1) without stabilizer, (2) with a sulphide of alkylated phenol as stabilizer, and (3) with phenyl - b - naphthylamine as stabilizer. The following compositions are mentioned: (1) 100 parts of the polymer of example 1, 40 parts carbon black, 10 parts of a tar residue sold under the Registered Trade Mark "Caoutchol," 5 parts zinc oxide, and 1 part each of sulphur and benzthiazyl - 2 - sulphene - diethyl - amide, vulcanization being effected for 40 minutes at 2,1 atmospheres pressure; and (2) 100 parts of the polymer of example 2, 10 parts zinc oxide, 10 parts titanium oxide, 1,5 parts each of sulphur and benzthiazyl - 2 - sulphene - diethylamide, and 2 parts stearic acid, vulcanization being effected for 60 minutes at 2,5 atmospheres pressure. The Provisional Specification refers to Specification 452,044, example 5, for the preparation of benzthiazyl-2-sulphene-diethylamide.ALSO:Synthetic rubber-like materials such as polymers of butadiene, isoprene, dimethyl butadiene, 2-chlor butadiene, and joint polymers of these substances with other polymerizable substances, such as styrene and acrylic nitrile, are stabilized by adding sulphides or polysulphides of alkylated phenols such as may be prepared by reacting an alkylated phenol with sulphur chloride or monochloride or by melting the alkylated phenol with sulphur. The stabilizer may be added to the solid polymer on the roller or to the synthetic latex where emulsion polymerization is employed. Examples described (1) and (2) the addition of di (tertiary and amyl phenol) disulphide to a synthetic latex prepared by emulsion polymerization of butadiene with acrylic nitrile and styrene respectively; (4) the addition of cresol sulphide to a latex from butadiene and acrylic nitrile; (5) the addition if diisobutyl sulphide to a latex from 2-chlorbutadiene. Particulars are given of the properties of the various polymers (1) without stabilizer, (2) with a sulphide of alkylated phenol as stabilizer, and (3) with phenyl-b -naphthylamine as stabilizer. The following compositions are mentioned, (1) 100 parts of the polymer of example 1, 40 parts carbon black, 10 parts a tar residue sold under the Registered Trade Mark "Caoutchol," 5 parts zinc oxide, and 1 part each of sulphur and benzthiazyl-2-sulphene-diethyl-amide, vulcanization being effected for 40 minutes at 2,1 atmospheres pressure; and (2) 100 parts of the polymer of example 2, 10 parts zinc oxide, 10 parts titanium oxide, 1,5 parts each of sulphur and benzthiazyl-2-sulphene-diethylamide, and 2 parts stearic acid, vulcanization being effected for 60 minutes at 2,5 atmospheres pressure. The Provisional Specification refers to Specification 452,044, [Group IV], example 5 for the preparation of benzthiazyl-2-sulphene-diethylamide.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1936I0056710 DE702210C (en) | 1936-12-25 | 1936-12-25 | rubber |
GB1147/37A GB488866A (en) | 1936-12-25 | 1937-01-14 | The manufacture of stable synthetic rubber |
FR831232D FR831232A (en) | 1936-12-25 | 1937-12-24 | Process for the stabilization of synthetic rubber-like products |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1936I0056710 DE702210C (en) | 1936-12-25 | 1936-12-25 | rubber |
GB1147/37A GB488866A (en) | 1936-12-25 | 1937-01-14 | The manufacture of stable synthetic rubber |
Publications (1)
Publication Number | Publication Date |
---|---|
GB488866A true GB488866A (en) | 1938-07-14 |
Family
ID=25981974
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1147/37A Expired GB488866A (en) | 1936-12-25 | 1937-01-14 | The manufacture of stable synthetic rubber |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE702210C (en) |
FR (1) | FR831232A (en) |
GB (1) | GB488866A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE900388C (en) * | 1941-05-27 | 1953-12-28 | Monsanto Chemicals | Process for the preservation of rubber |
DE952938C (en) * | 1943-02-28 | 1956-12-27 | Bayer Ag | Process for stabilizing synthetic rubber obtained by emulsion polymerization |
-
1936
- 1936-12-25 DE DE1936I0056710 patent/DE702210C/en not_active Expired
-
1937
- 1937-01-14 GB GB1147/37A patent/GB488866A/en not_active Expired
- 1937-12-24 FR FR831232D patent/FR831232A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE702210C (en) | 1941-02-01 |
FR831232A (en) | 1938-08-26 |
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