GB815939A - Vulcanizing compositions comprising chlorinated butyl rubber - Google Patents
Vulcanizing compositions comprising chlorinated butyl rubberInfo
- Publication number
- GB815939A GB815939A GB1793/57A GB179357A GB815939A GB 815939 A GB815939 A GB 815939A GB 1793/57 A GB1793/57 A GB 1793/57A GB 179357 A GB179357 A GB 179357A GB 815939 A GB815939 A GB 815939A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- amino
- methylamino
- phenyl
- nitro
- 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
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)
- Processes Of Treating Macromolecular Substances (AREA)
Abstract
Chlorinated butyl rubber is vulcanized by compounding with an organic nitrogen-containing compound having (1) at least one -NH2 group, (2) at least one -NH2 group and at least one -NH- group, (3) at least two -NH-groups, or (4) a compound which under vulcanizing conditions, forms the nitrogen groups in situ; or mixtures thereof, and curing in the absence of sulphur. The butyl rubber contains a major proportion of iso-olefines, e.g. isobutylene, 2-methyl butene-1, and a minor proportion of diolefines, e.g. isoprene, dimethyl butadiene, piperylene, cyclopentadiene, myrcene, 1-vinylcyclohexene-1,3, and dimethyl fulvene, chlorinated to contain at least 0.5 wt. per cent of combined chlorine but not more than one combined atom of chlorine per double bond in the copolymer. The nitrogen-containing organic compounds may be present in an amount of from 0.1 to 20 weight per cent based on the weight of the chlorinated rubber, and examples are monofunctional primary amines, such as hexyl-, octyl-, decyl-, hexadecyl-, dodecyl-, dimethyl pentyl-, pentamethyl hexyl-, methyl octyl-, diethyl heptyl-, 9-hexadecyl-, a - or b -phenyl ethyl-amines; and naphthyl- and hydrogenated naphthylamines; phenyl-, ethyl-, t-butyl and 2,4,6-trimethyl anilines; toluidines; formaldehyde-p-toluidine reaction products; 2-amino- and 2-methylamino-4-chlorotoluene, 5-amino-1- and 5-methylamino-1-naphthols; o-m- and p-amino-, 2-amino-4-nitro, 2-amino-4-phenyl-, and 2-methylamino-4-phenyl phenols; p-methyl, p-amino and p-methylamino phenyl-acetic acids; p-methyl and p-methylaminophenylacetonitriles; p-amino and p-isopropylamino propriophenones; 4-chloro-, 4-nitro-, 4-chloro-N-methyl-, and 4-nitro-N-methyl anilines, 2-amino-, 2-amino-3-methyl-, 2-amino-4-methyl-, 2-amino-5-methyl-, 2-amino-6-methyl-, 2 - methylamino - 3 - methyl -, 2 - ethylamino - 4 - methyl -, 2 - hexylamino - 5 - methyl -, 2 - methylamino - 6 - methyl -, and 2 - methylamino - pyridines; 3-amino-, 8-amino-, 3-methylamino-, 8-heptylamino-quinolines; ethanolamine and N-methyl ethanolamine; glycine and N-methyl glycine; b -alanine and N-methyl b -alanine; 4-nitro- and N-methyl-4-nitrobenzylamine; b -aminoproprionitrile; a -aminoacetamide; m-(p-anilinophenylazo)- and p-amino-benzene sulphonic acid; b -chloroethylamine; and N-methyl anthranilic and sulphanilic acids. Optional ingredients may be zinc, magnesium, calcium and lead oxides or basic metallo-organic lead stearate or mixtures thereof; pigments and fillers such as titanium dioxide, clays, ultramarine blue, carbon black, silica, calcium carbonate, ferric hydroxide, chrome yellow, and Prussion blue; tackifiers such as phenol or p-toluidine formaldehyde resins; accelerators and calcium silicate and the composition may be vulcanized at from 270-400 DEG F. The vulcanized composition may be used in tyres, electrical insulation, tyre curing bags, car window channels and tie-ply compositions, and proofed goods.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US840005XA | 1956-08-01 | 1956-08-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB815939A true GB815939A (en) | 1959-07-01 |
Family
ID=22182005
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1793/57A Expired GB815939A (en) | 1956-08-01 | 1957-01-17 | Vulcanizing compositions comprising chlorinated butyl rubber |
GB22150/57A Expired GB840005A (en) | 1956-08-01 | 1957-07-12 | Vulcanizing brominated polymers |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB22150/57A Expired GB840005A (en) | 1956-08-01 | 1957-07-12 | Vulcanizing brominated polymers |
Country Status (3)
Country | Link |
---|---|
FR (1) | FR1172154A (en) |
GB (2) | GB815939A (en) |
NL (3) | NL106519C (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3397174A (en) * | 1964-09-10 | 1968-08-13 | Exxon Research Engineering Co | Stabilizing halogenated copolymers |
CN110577709A (en) * | 2019-09-09 | 2019-12-17 | 四川大学 | High-mechanical-property self-repairing halogenated butyl rubber material and preparation method thereof |
CN110628143A (en) * | 2019-09-09 | 2019-12-31 | 四川大学 | Fluorine-chlorine elastomer material with various excellent performances and preparation method thereof |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1482839A (en) * | 1974-10-29 | 1977-08-17 | Sanyo Trading Co | Vulcanisable rubber compositions and vulcanised rubber prepared therefrom |
US4325865A (en) * | 1977-11-02 | 1982-04-20 | Monsanto Company | Flame retardant resin compositions |
-
0
- NL NL104398D patent/NL104398C/xx active
- NL NL214400D patent/NL214400A/xx unknown
- NL NL106519D patent/NL106519C/xx active
-
1957
- 1957-01-17 GB GB1793/57A patent/GB815939A/en not_active Expired
- 1957-01-30 FR FR1172154D patent/FR1172154A/en not_active Expired
- 1957-07-12 GB GB22150/57A patent/GB840005A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3397174A (en) * | 1964-09-10 | 1968-08-13 | Exxon Research Engineering Co | Stabilizing halogenated copolymers |
CN110577709A (en) * | 2019-09-09 | 2019-12-17 | 四川大学 | High-mechanical-property self-repairing halogenated butyl rubber material and preparation method thereof |
CN110628143A (en) * | 2019-09-09 | 2019-12-31 | 四川大学 | Fluorine-chlorine elastomer material with various excellent performances and preparation method thereof |
CN110577709B (en) * | 2019-09-09 | 2021-01-05 | 四川大学 | High-mechanical-property self-repairing halogenated butyl rubber material and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
NL104398C (en) | |
NL214400A (en) | |
GB840005A (en) | 1960-07-06 |
FR1172154A (en) | 1959-02-06 |
NL106519C (en) |
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