GB1001364A - Process of manufacturing epoxide resins - Google Patents
Process of manufacturing epoxide resinsInfo
- Publication number
- GB1001364A GB1001364A GB14269/62A GB1426962A GB1001364A GB 1001364 A GB1001364 A GB 1001364A GB 14269/62 A GB14269/62 A GB 14269/62A GB 1426962 A GB1426962 A GB 1426962A GB 1001364 A GB1001364 A GB 1001364A
- Authority
- GB
- United Kingdom
- Prior art keywords
- water
- polar
- resin
- alkali
- xylene
- 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
- 229920000647 polyepoxide Polymers 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 229920005989 resin Polymers 0.000 abstract 6
- 239000011347 resin Substances 0.000 abstract 6
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 239000003513 alkali Substances 0.000 abstract 3
- 239000002798 polar solvent Substances 0.000 abstract 3
- 239000002904 solvent Substances 0.000 abstract 3
- 229920003169 water-soluble polymer Polymers 0.000 abstract 3
- 239000008096 xylene Substances 0.000 abstract 3
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 2
- 239000011324 bead Substances 0.000 abstract 2
- 239000000084 colloidal system Substances 0.000 abstract 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 abstract 2
- 239000012535 impurity Substances 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 239000012454 non-polar solvent Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 abstract 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 abstract 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000004372 Polyvinyl alcohol Substances 0.000 abstract 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 239000001768 carboxy methyl cellulose Substances 0.000 abstract 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 abstract 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 238000001704 evaporation Methods 0.000 abstract 1
- 238000001914 filtration Methods 0.000 abstract 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 abstract 1
- 229920002451 polyvinyl alcohol Polymers 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- 230000001681 protective effect Effects 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 238000003756 stirring Methods 0.000 abstract 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
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/04—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
- C08G59/06—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
- C08G59/063—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols with epihalohydrins
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL9624361 | 1961-04-13 | ||
| PL9796961 | 1961-12-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1001364A true GB1001364A (en) | 1965-08-18 |
Family
ID=26652438
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB14269/62A Expired GB1001364A (en) | 1961-04-13 | 1962-04-12 | Process of manufacturing epoxide resins |
Country Status (6)
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006111810A2 (en) | 2005-04-18 | 2006-10-26 | Aser S.R.L. | Process for the production of alpha, gamma-dichlorohydrin from glycerin and hydrochloric acid |
| CN101003614B (zh) * | 2003-11-20 | 2010-10-27 | 索尔维公司 | 用于生产环氧树脂的方法 |
| WO2015033365A1 (en) | 2013-09-03 | 2015-03-12 | Eurochem Engineering Srl | Process for the production of dichlorohydrons |
| WO2016009344A1 (en) | 2014-07-17 | 2016-01-21 | Conser Spa | Process for the production of chlorohydrins from glycerol and acyl chlorides |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4122067A (en) * | 1977-10-07 | 1978-10-24 | Celanese Polymer Specialties Company | Process of reacting a polyepoxide compound with a phenol in aqueous medium |
| US4696982A (en) * | 1986-09-17 | 1987-09-29 | The Dow Chemical Company | Process for removing residual salts from epoxy novolacs |
| EP2470582B1 (en) | 2009-08-24 | 2015-05-27 | Dow Global Technologies LLC | Method of making a particulate epoxy resin |
| JP2015500394A (ja) * | 2011-12-19 | 2015-01-05 | ダウ グローバル テクノロジーズ エルエルシー | エポキシ樹脂生成 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2686771A (en) * | 1950-12-23 | 1954-08-17 | Sherwin Williams Co | Acid-modified ether resins |
| US2694694A (en) * | 1952-10-17 | 1954-11-16 | Devoe & Raynolds Co | Manufacture of epoxide resins |
| NL103227C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1953-04-06 | |||
| DE1016273B (de) * | 1953-10-19 | 1957-09-26 | Bataafsche Petroleum | Verfahren zur Herstellung von Glycidylaethern mehrwertiger Phenole |
| US2824855A (en) * | 1954-12-20 | 1958-02-25 | Freeman Chemical Corp | Preparation of epoxide resins |
| GB785415A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1955-01-31 | |||
| US2886472A (en) * | 1956-04-27 | 1959-05-12 | Shell Dev | Treatment of textile materials |
-
0
- NL NL277243D patent/NL277243A/xx unknown
-
1962
- 1962-04-05 US US185241A patent/US3296157A/en not_active Expired - Lifetime
- 1962-04-10 CH CH435962A patent/CH438745A/de unknown
- 1962-04-12 GB GB14269/62A patent/GB1001364A/en not_active Expired
- 1962-04-13 FR FR894461A patent/FR1319795A/fr not_active Expired
- 1962-04-13 DE DEJ21609A patent/DE1257786B/de active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101003614B (zh) * | 2003-11-20 | 2010-10-27 | 索尔维公司 | 用于生产环氧树脂的方法 |
| WO2006111810A2 (en) | 2005-04-18 | 2006-10-26 | Aser S.R.L. | Process for the production of alpha, gamma-dichlorohydrin from glycerin and hydrochloric acid |
| WO2015033365A1 (en) | 2013-09-03 | 2015-03-12 | Eurochem Engineering Srl | Process for the production of dichlorohydrons |
| WO2016009344A1 (en) | 2014-07-17 | 2016-01-21 | Conser Spa | Process for the production of chlorohydrins from glycerol and acyl chlorides |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1257786B (de) | 1968-01-04 |
| NL277243A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| CH438745A (de) | 1967-06-30 |
| US3296157A (en) | 1967-01-03 |
| FR1319795A (fr) | 1963-03-01 |
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