GB611919A - A process for the manufacture of valuable reaction products of high-molecular unsaturated substances containing more than one unsaturated grouping in the molecule with inorganic acids or acid anhydrides - Google Patents
A process for the manufacture of valuable reaction products of high-molecular unsaturated substances containing more than one unsaturated grouping in the molecule with inorganic acids or acid anhydridesInfo
- Publication number
- GB611919A GB611919A GB32455/45A GB3245545A GB611919A GB 611919 A GB611919 A GB 611919A GB 32455/45 A GB32455/45 A GB 32455/45A GB 3245545 A GB3245545 A GB 3245545A GB 611919 A GB611919 A GB 611919A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ether
- unsaturated
- copolymers
- acids
- oxygen
- 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
- 239000000126 substance Substances 0.000 title abstract 11
- 150000007522 mineralic acids Chemical class 0.000 title abstract 4
- 150000008065 acid anhydrides Chemical class 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title abstract 3
- 239000007795 chemical reaction product Substances 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 18
- 239000000203 mixture Substances 0.000 abstract 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 6
- 229920001577 copolymer Polymers 0.000 abstract 6
- 230000003647 oxidation Effects 0.000 abstract 6
- 238000007254 oxidation reaction Methods 0.000 abstract 6
- 229920000642 polymer Polymers 0.000 abstract 6
- 239000002253 acid Substances 0.000 abstract 5
- ZGHFDIIVVIFNPS-UHFFFAOYSA-N 3-Methyl-3-buten-2-one Chemical compound CC(=C)C(C)=O ZGHFDIIVVIFNPS-UHFFFAOYSA-N 0.000 abstract 4
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 abstract 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 4
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 4
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 abstract 4
- 238000006243 chemical reaction Methods 0.000 abstract 4
- 150000001993 dienes Chemical class 0.000 abstract 4
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 abstract 4
- 125000002534 ethynyl group Chemical class [H]C#C* 0.000 abstract 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- 244000043261 Hevea brasiliensis Species 0.000 abstract 3
- 150000007513 acids Chemical class 0.000 abstract 3
- 150000008064 anhydrides Chemical class 0.000 abstract 3
- 229920003052 natural elastomer Polymers 0.000 abstract 3
- 229920001194 natural rubber Polymers 0.000 abstract 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 2
- XDJWZONZDVNKDU-UHFFFAOYSA-N 1314-24-5 Chemical compound O=POP=O XDJWZONZDVNKDU-UHFFFAOYSA-N 0.000 abstract 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 abstract 2
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 abstract 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical class Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 abstract 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 abstract 2
- 239000005062 Polybutadiene Substances 0.000 abstract 2
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 abstract 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 abstract 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 239000007864 aqueous solution Substances 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 2
- 238000004040 coloring Methods 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 238000000354 decomposition reaction Methods 0.000 abstract 2
- LZDSILRDTDCIQT-UHFFFAOYSA-N dinitrogen trioxide Chemical compound [O-][N+](=O)N=O LZDSILRDTDCIQT-UHFFFAOYSA-N 0.000 abstract 2
- 150000002170 ethers Chemical class 0.000 abstract 2
- 239000000945 filler Substances 0.000 abstract 2
- 239000011888 foil Substances 0.000 abstract 2
- 125000005395 methacrylic acid group Chemical class 0.000 abstract 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 230000001590 oxidative effect Effects 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 abstract 2
- 239000004014 plasticizer Substances 0.000 abstract 2
- 229920002857 polybutadiene Polymers 0.000 abstract 2
- 239000000243 solution Substances 0.000 abstract 2
- 239000003381 stabilizer Substances 0.000 abstract 2
- 239000004291 sulphur dioxide Substances 0.000 abstract 2
- 235000010269 sulphur dioxide Nutrition 0.000 abstract 2
- -1 tetrahydronaphthalene peroxides Chemical class 0.000 abstract 2
- 229920001567 vinyl ester resin Polymers 0.000 abstract 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 2
- 241001323490 Colias gigantea Species 0.000 abstract 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 abstract 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene group Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 1
- WFYPICNXBKQZGB-UHFFFAOYSA-N butenyne Chemical group C=CC#C WFYPICNXBKQZGB-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 235000019441 ethanol Nutrition 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- VSAISIQCTGDGPU-UHFFFAOYSA-N phosphorus trioxide Inorganic materials O1P(O2)OP3OP1OP2O3 VSAISIQCTGDGPU-UHFFFAOYSA-N 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/24—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of aliphatic compounds with more than one carbon-to-carbon double bond
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (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)
- Laminated Bodies (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL611919X | 1941-12-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB611919A true GB611919A (en) | 1948-11-05 |
Family
ID=19788128
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB32455/45A Expired GB611919A (en) | 1941-12-23 | 1945-11-30 | A process for the manufacture of valuable reaction products of high-molecular unsaturated substances containing more than one unsaturated grouping in the molecule with inorganic acids or acid anhydrides |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE478000A (enrdf_load_stackoverflow) |
| DE (1) | DE896107C (enrdf_load_stackoverflow) |
| FR (1) | FR888998A (enrdf_load_stackoverflow) |
| GB (1) | GB611919A (enrdf_load_stackoverflow) |
| NL (1) | NL59013C (enrdf_load_stackoverflow) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2988531A (en) * | 1958-11-19 | 1961-06-13 | Exxon Research Engineering Co | Vulcanization of butyl rubber with a 2, 6-dimethylol-4-hydrocarbon substituted phenol and phosphorus pentoxide |
| US3036978A (en) * | 1958-07-08 | 1962-05-29 | Degussa | Dissolved copolymers of aqueous solutions of so containing acrolein and a member from the group consisting of acrylonitrile, methyl methacrylate, and vinyl acetate |
-
0
- BE BE478000D patent/BE478000A/xx unknown
- NL NL59013D patent/NL59013C/xx active
-
1942
- 1942-11-25 DE DEN1552D patent/DE896107C/de not_active Expired
- 1942-12-10 FR FR888998D patent/FR888998A/fr not_active Expired
-
1945
- 1945-11-30 GB GB32455/45A patent/GB611919A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3036978A (en) * | 1958-07-08 | 1962-05-29 | Degussa | Dissolved copolymers of aqueous solutions of so containing acrolein and a member from the group consisting of acrylonitrile, methyl methacrylate, and vinyl acetate |
| US2988531A (en) * | 1958-11-19 | 1961-06-13 | Exxon Research Engineering Co | Vulcanization of butyl rubber with a 2, 6-dimethylol-4-hydrocarbon substituted phenol and phosphorus pentoxide |
Also Published As
| Publication number | Publication date |
|---|---|
| FR888998A (fr) | 1943-12-28 |
| DE896107C (de) | 1953-11-09 |
| NL59013C (enrdf_load_stackoverflow) | |
| BE478000A (enrdf_load_stackoverflow) |
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