DE1237313B - Vernetzen von amorphen Epihalogenhydrinpolymeren oder -mischpolymeren - Google Patents
Vernetzen von amorphen Epihalogenhydrinpolymeren oder -mischpolymerenInfo
- Publication number
- DE1237313B DE1237313B DEH42496A DEH0042496A DE1237313B DE 1237313 B DE1237313 B DE 1237313B DE H42496 A DEH42496 A DE H42496A DE H0042496 A DEH0042496 A DE H0042496A DE 1237313 B DE1237313 B DE 1237313B
- Authority
- DE
- Germany
- Prior art keywords
- crosslinking
- amorphous
- copolymers
- polymer
- epihalohydrin polymers
- 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.)
- Pending
Links
- 229920000642 polymer Polymers 0.000 title claims description 21
- 238000004132 cross linking Methods 0.000 title claims description 12
- 229920001577 copolymer Polymers 0.000 title description 3
- 229920000768 polyamine Polymers 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims description 3
- 239000002738 chelating agent Substances 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 150000001412 amines Chemical class 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000004073 vulcanization Methods 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 125000003700 epoxy group Chemical group 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- XSQHUYDRSDBCHN-UHFFFAOYSA-N 2,3-dimethyl-2-propan-2-ylbutanenitrile Chemical compound CC(C)C(C)(C#N)C(C)C XSQHUYDRSDBCHN-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- -1 aliphatic Amines Chemical class 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 125000004970 halomethyl group Chemical group 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- VJOWMORERYNYON-UHFFFAOYSA-N 5-ethenyl-2-methylpyridine Chemical compound CC1=CC=C(C=C)C=N1 VJOWMORERYNYON-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 241000779819 Syncarpia glomulifera Species 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000005263 alkylenediamine group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- YXIWHUQXZSMYRE-UHFFFAOYSA-N benzothiazolyl mercaptan Natural products C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- LZDHIQDKAYUDND-UHFFFAOYSA-N biphenylene-1,2-diamine Chemical compound C1=CC=C2C3=C(N)C(N)=CC=C3C2=C1 LZDHIQDKAYUDND-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 238000005097 cold rolling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- NTNWKDHZTDQSST-UHFFFAOYSA-N naphthalene-1,2-diamine Chemical compound C1=CC=CC2=C(N)C(N)=CC=C21 NTNWKDHZTDQSST-UHFFFAOYSA-N 0.000 description 1
- 230000006855 networking Effects 0.000 description 1
- 230000001537 neural effect Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000001739 pinus spp. Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002755 poly(epichlorohydrin) Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 239000007965 rubber solvent Substances 0.000 description 1
- 238000013040 rubber vulcanization Methods 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 229940036248 turpentine Drugs 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc oxide Inorganic materials [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
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
- C08K5/205—Compounds containing groups, e.g. carbamates
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/06—Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
- C08G65/08—Saturated oxiranes
- C08G65/10—Saturated oxiranes characterised by the catalysts used
- C08G65/12—Saturated oxiranes characterised by the catalysts used containing organo-metallic compounds or metal hydrides
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/22—Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
- C08G65/24—Epihalohydrins
-
- 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
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/02—Organic and inorganic ingredients
-
- 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
-
- 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
- C08K5/39—Thiocarbamic acids; Derivatives thereof, e.g. dithiocarbamates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
- C08L71/03—Polyepihalohydrins
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Sealing Material Composition (AREA)
- Polyethers (AREA)
- Polymerization Catalysts (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Epoxy Resins (AREA)
Applications Claiming Priority (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73863258A | 1958-05-29 | 1958-05-29 | |
| US73865158A | 1958-05-29 | 1958-05-29 | |
| US73862758A | 1958-05-29 | 1958-05-29 | |
| US73865058A | 1958-05-29 | 1958-05-29 | |
| US73863358A | 1958-05-29 | 1958-05-29 | |
| US73862658A | 1958-05-29 | 1958-05-29 | |
| US73862558A | 1958-05-29 | 1958-05-29 | |
| US738629A US3026270A (en) | 1958-05-29 | 1958-05-29 | Cross-linking of polymeric epoxides |
| US812080A US3135706A (en) | 1959-05-11 | 1959-05-11 | Polymeric epoxides |
| US812079A US3135705A (en) | 1959-05-11 | 1959-05-11 | Polymeric epoxides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1237313B true DE1237313B (de) | 1967-03-23 |
Family
ID=27581317
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEH42496A Pending DE1237313B (de) | 1958-05-29 | 1959-05-29 | Vernetzen von amorphen Epihalogenhydrinpolymeren oder -mischpolymeren |
| DE1959H0036503 Pending DE1130599B (de) | 1958-05-29 | 1959-05-29 | Verfahren zur Homo- oder Mischpolymerisation von monomeren Epoxydverbindungen |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1959H0036503 Pending DE1130599B (de) | 1958-05-29 | 1959-05-29 | Verfahren zur Homo- oder Mischpolymerisation von monomeren Epoxydverbindungen |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE579074A (en, 2012) |
| DE (2) | DE1237313B (en, 2012) |
| FR (1) | FR1229090A (en, 2012) |
| GB (1) | GB898306A (en, 2012) |
| LU (1) | LU37244A1 (en, 2012) |
| NL (5) | NL125852C (en, 2012) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1249247B (de) * | 1961-04-25 | 1967-09-07 | E. I. Du Pont De Nemours And Company, Wilmington, Del. (V. St. A.) | Verfahren zur Herstellung von Perfluorolefinpolyäthern |
| US4233425A (en) | 1978-11-15 | 1980-11-11 | The Dow Chemical Company | Addition polymerizable polyethers having pendant ethylenically unsaturated urethane groups |
| FR2570224B1 (fr) * | 1984-09-11 | 1987-03-20 | Elf Aquitaine | Electrolyte solide polymere constitue par un copolymere reticule |
| US4686273A (en) * | 1985-07-01 | 1987-08-11 | The Dow Chemical Company | Process for preparing modified poly(alkylene carbonate) polyahls |
| US4668710A (en) * | 1985-12-23 | 1987-05-26 | The Dow Chemical Company | Trihalovinyl polyol ethers |
| US4734443A (en) * | 1986-04-21 | 1988-03-29 | The Dow Chemical Company | Polyurethanes with mono-ol/diol haloneocarbyl polyethers and their esters |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2801229A (en) * | 1953-07-29 | 1957-07-30 | Shell Dev | Curing glycidyl polyethers |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE544935A (en, 2012) * | 1955-02-04 | 1900-01-01 | ||
| GB793065A (en) * | 1955-08-22 | 1958-04-09 | Petrochemicals Ltd | Improvements in or relating to the production of alkylene oxide co-polymers |
| BE566483A (en, 2012) * | 1957-04-05 |
-
0
- NL NL239640D patent/NL239640A/xx unknown
-
1959
- 1959-05-27 LU LU37244D patent/LU37244A1/xx unknown
- 1959-05-27 BE BE579074D patent/BE579074A/xx unknown
- 1959-05-28 NL NL239640A patent/NL125852C/xx active
- 1959-05-29 GB GB1842559A patent/GB898306A/en not_active Expired
- 1959-05-29 FR FR69039463A patent/FR1229090A/fr not_active Expired
- 1959-05-29 DE DEH42496A patent/DE1237313B/de active Pending
- 1959-05-29 DE DE1959H0036503 patent/DE1130599B/de active Pending
-
1967
- 1967-01-30 NL NL6701446A patent/NL132495C/xx active
- 1967-01-30 NL NL6701445A patent/NL130566C/xx active
-
1968
- 1968-11-08 NL NL6815971A patent/NL6815971A/xx unknown
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2801229A (en) * | 1953-07-29 | 1957-07-30 | Shell Dev | Curing glycidyl polyethers |
Also Published As
| Publication number | Publication date |
|---|---|
| LU37244A1 (en, 2012) | 1959-07-27 |
| NL130566C (en, 2012) | 1971-01-15 |
| NL125852C (en, 2012) | 1969-01-15 |
| BE579074A (en, 2012) | 1959-06-15 |
| GB898306A (en) | 1962-06-06 |
| NL132495C (en, 2012) | 1971-10-15 |
| NL6815971A (en, 2012) | 1969-01-27 |
| NL6701446A (en, 2012) | 1967-04-25 |
| DE1130599B (de) | 1962-05-30 |
| NL239640A (en, 2012) | |
| FR1229090A (fr) | 1960-09-02 |
| NL6701445A (en, 2012) | 1967-04-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2541234C3 (de) | Kationische elektrophoretische Beschichtungsmassen | |
| DE3855056T2 (de) | Verfahren zur Herstellung reiner primärer Diamine | |
| DE2019758C3 (de) | Verfahren zur Herstellung von Epoxypolyaddukten | |
| DE2141807C2 (de) | Selbstemulgierter wäßriger Polyurethanharnstoff- oder Polyharnstoff-Latex und dessen Verwendung zur Herstellung von Filmen | |
| DE2321827A1 (de) | Haerten von polymeren oder vorpolymeren mit komplexen aus ausgewaehlten diaminen und alkalisalzen | |
| DE1814832A1 (de) | Hydroxylmethylgruppen aufweisende Aldimine bzw. Ketimine und ein Verfahren zu ihrer Herstellung | |
| DE1164088B (de) | Verfahren zum Vernetzen polymerer Verbindungen | |
| DE2448682A1 (de) | Vernetzte quaternisierte epihalogenhydrinpolymerisate | |
| DE1237313B (de) | Vernetzen von amorphen Epihalogenhydrinpolymeren oder -mischpolymeren | |
| EP0000561B1 (de) | Wasserlösliche, vernetzte stickstoffhaltige Kondensationsprodukte und deren Verwendung | |
| DE2003016A1 (de) | Neue Diglydicylderivate von zwei N-heterocyclische Ringe enthaltenden Verbindungen,Verfahren zu ihrer Herstellung und Anwendung | |
| DE1569073A1 (de) | Verfahren zum Vernetzen eines linearen gesaettigten Polymerisats | |
| DE1244410B (de) | Verfahren zur Herstellung von vernetzbaren hochmolekularen Polymerisations-, Polykondensations- und Polyadditionsprodukten | |
| EP0496218A2 (de) | Pigmentdruck auf Faserstoffen | |
| DE847347C (de) | Verfahren zur Herstellung von Polymerisaten | |
| DE1242871B (de) | Verfahren zur Herstellung von stickstoffhaltigen Copolymerisaten | |
| EP0560190B1 (de) | Bindemittel für die Elektrotauchlackierung | |
| DE2262157C2 (de) | Niedrigviskose, halogenhaltige selbstverlöschende Epoxidharze, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| DE2339237A1 (de) | 4,4'-diaminodiphenylmethane, verfahren zu ihrer herstellung und ihre verwendung als haerter fuer epoxyharze | |
| EP0579081B1 (de) | Bindemittelsystem | |
| DE1420796A1 (de) | Verfahren zur Herstellung synthetischer Harze | |
| DE1199498C2 (de) | Verfahren zum Herstellen basischer Polyamide | |
| DE2719718A1 (de) | Verfahren zur herstellung niedermolekularer c tief 2 -c tief 3 -alkylen- bzw. poly-c tief 2 -c tief 3-alkylen- polyamine | |
| EP0029094B1 (de) | In der Wärme einzubrennende wässrige Überzugsmittel für die anodische Elektrotauchlackierung | |
| DE1570853C (de) | Verfahren zur Herstellung von Amino gruppen aufweisenden Oxymethylencopolymen säten |