DE2331289C3 - Epoxidverbindungen - Google Patents
EpoxidverbindungenInfo
- Publication number
- DE2331289C3 DE2331289C3 DE2331289A DE2331289A DE2331289C3 DE 2331289 C3 DE2331289 C3 DE 2331289C3 DE 2331289 A DE2331289 A DE 2331289A DE 2331289 A DE2331289 A DE 2331289A DE 2331289 C3 DE2331289 C3 DE 2331289C3
- Authority
- DE
- Germany
- Prior art keywords
- epoxy
- epoxy compounds
- mixture
- temperature
- weight
- 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
- 239000004593 Epoxy Substances 0.000 title claims description 31
- 150000001875 compounds Chemical class 0.000 title claims description 18
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 12
- 239000004800 polyvinyl chloride Substances 0.000 claims description 11
- 229920000642 polymer Polymers 0.000 claims description 7
- 229920002396 Polyurea Polymers 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 3
- 229920002635 polyurethane Polymers 0.000 claims description 3
- 239000004814 polyurethane Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 description 26
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- 229920000647 polyepoxide Polymers 0.000 description 14
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 11
- 238000009472 formulation Methods 0.000 description 10
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 10
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 9
- 150000002118 epoxides Chemical class 0.000 description 9
- 239000000047 product Substances 0.000 description 8
- 150000001336 alkenes Chemical class 0.000 description 7
- 125000003700 epoxy group Chemical group 0.000 description 7
- 239000003822 epoxy resin Substances 0.000 description 7
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- -1 vinylidene olefins Chemical class 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 230000009102 absorption Effects 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 239000004711 α-olefin Substances 0.000 description 6
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 235000019253 formic acid Nutrition 0.000 description 5
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- 230000008014 freezing Effects 0.000 description 4
- 238000007710 freezing Methods 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000006735 epoxidation reaction Methods 0.000 description 3
- 238000004817 gas chromatography Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 238000002329 infrared spectrum Methods 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 3
- BHFSSZVURVDPON-UHFFFAOYSA-N 2-butyl-2-hexyloxirane Chemical compound CCCCCCC1(CCCC)CO1 BHFSSZVURVDPON-UHFFFAOYSA-N 0.000 description 2
- FYVVJJSVACJWEP-UHFFFAOYSA-N 2-dodecyl-2-octyloxirane Chemical compound CCCCCCCCCCCCC1(CCCCCCCC)CO1 FYVVJJSVACJWEP-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 1
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
- KQIMLRIWIRBYGZ-UHFFFAOYSA-N 2,2-didecyloxirane Chemical compound CCCCCCCCCCC1(CCCCCCCCCC)CO1 KQIMLRIWIRBYGZ-UHFFFAOYSA-N 0.000 description 1
- ACQWWHURYSEHBH-UHFFFAOYSA-N 2-decyl-2-octyloxirane Chemical compound CCCCCCCCCCC1(CCCCCCCC)CO1 ACQWWHURYSEHBH-UHFFFAOYSA-N 0.000 description 1
- UXBBGMSRUZZQEA-UHFFFAOYSA-N 2-hexyloxiran-2-ol Chemical compound OC1(CO1)CCCCCC UXBBGMSRUZZQEA-UHFFFAOYSA-N 0.000 description 1
- NJWSNNWLBMSXQR-UHFFFAOYSA-N 2-hexyloxirane Chemical compound CCCCCCC1CO1 NJWSNNWLBMSXQR-UHFFFAOYSA-N 0.000 description 1
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 230000000447 dimerizing effect Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1433—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
- C08G59/1438—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing oxygen
- C08G59/145—Compounds containing one epoxy group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/04—Compounds containing oxirane rings containing only hydrogen and carbon atoms in addition to the ring oxygen atoms
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1515—Three-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Emergency Medicine (AREA)
- Epoxy Compounds (AREA)
- Epoxy Resins (AREA)
- Polyurethanes Or Polyureas (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Photoreceptors In Electrophotography (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US00263678A US3835166A (en) | 1972-06-16 | 1972-06-16 | 2,2-dialkylepoxides |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2331289A1 DE2331289A1 (de) | 1974-01-10 |
| DE2331289B2 DE2331289B2 (enExample) | 1974-08-29 |
| DE2331289C3 true DE2331289C3 (de) | 1978-11-30 |
Family
ID=23002799
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2331289A Expired DE2331289C3 (de) | 1972-06-16 | 1973-06-15 | Epoxidverbindungen |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3835166A (enExample) |
| JP (1) | JPS5427321B2 (enExample) |
| BE (1) | BE800945A (enExample) |
| CA (1) | CA1080873A (enExample) |
| DE (1) | DE2331289C3 (enExample) |
| FR (1) | FR2189396B1 (enExample) |
| GB (1) | GB1430955A (enExample) |
| NL (1) | NL153192B (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4127542A (en) * | 1975-12-15 | 1978-11-28 | American Cyanamid Company | Stabilization of polyester urethanes using organic epoxides |
| US4243598A (en) * | 1977-05-17 | 1981-01-06 | Hoffmann-La Roche Inc. | Synthesis of vitamin E |
| EP0052424B2 (en) * | 1980-11-19 | 1990-02-28 | Imperial Chemical Industries Plc | Triazole compounds, a process for preparing them, their use as plant fungicides and fungicidal compositions containing them |
| US8318648B2 (en) * | 2009-12-15 | 2012-11-27 | Exxonmobil Research And Engineering Company | Polyether-containing lubricant base stocks and process for making |
| CN116355169B (zh) * | 2023-03-09 | 2025-01-03 | 亚培烯科技(上海)有限公司 | 聚合物及其制备方法和用途 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5239065A (en) * | 1975-09-20 | 1977-03-26 | Fuji Electric Co Ltd | Reciprocating rectlinear motion mechanism |
-
1972
- 1972-06-16 US US00263678A patent/US3835166A/en not_active Expired - Lifetime
-
1973
- 1973-04-26 CA CA169,614A patent/CA1080873A/en not_active Expired
- 1973-06-12 GB GB2794873A patent/GB1430955A/en not_active Expired
- 1973-06-15 DE DE2331289A patent/DE2331289C3/de not_active Expired
- 1973-06-15 FR FR7321939A patent/FR2189396B1/fr not_active Expired
- 1973-06-15 BE BE1005158A patent/BE800945A/xx unknown
- 1973-06-15 NL NL737308404A patent/NL153192B/xx not_active IP Right Cessation
- 1973-06-16 JP JP6823973A patent/JPS5427321B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| US3835166A (en) | 1974-09-10 |
| DE2331289B2 (enExample) | 1974-08-29 |
| CA1080873A (en) | 1980-07-01 |
| JPS5427321B2 (enExample) | 1979-09-10 |
| JPS4961106A (enExample) | 1974-06-13 |
| GB1430955A (en) | 1976-04-07 |
| BE800945A (fr) | 1973-12-17 |
| FR2189396B1 (enExample) | 1976-07-23 |
| FR2189396A1 (enExample) | 1974-01-25 |
| DE2331289A1 (de) | 1974-01-10 |
| NL7308404A (enExample) | 1973-12-18 |
| NL153192B (nl) | 1977-05-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) | ||
| 8339 | Ceased/non-payment of the annual fee |