GB877670A - Process for the production of modified melamine resins - Google Patents
Process for the production of modified melamine resinsInfo
- Publication number
- GB877670A GB877670A GB25419/59A GB2541959A GB877670A GB 877670 A GB877670 A GB 877670A GB 25419/59 A GB25419/59 A GB 25419/59A GB 2541959 A GB2541959 A GB 2541959A GB 877670 A GB877670 A GB 877670A
- Authority
- GB
- United Kingdom
- Prior art keywords
- urea
- polyamide
- melamine
- amino groups
- formaldehyde
- 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
- 229920000877 Melamine resin Polymers 0.000 title abstract 6
- 150000007974 melamines Chemical class 0.000 title 1
- 239000004952 Polyamide Substances 0.000 abstract 8
- 229920002647 polyamide Polymers 0.000 abstract 8
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 7
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 abstract 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 6
- 239000004202 carbamide Substances 0.000 abstract 6
- 229920000768 polyamine Polymers 0.000 abstract 6
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 abstract 5
- 125000003277 amino group Chemical group 0.000 abstract 5
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 abstract 5
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 abstract 3
- 229960004279 formaldehyde Drugs 0.000 abstract 3
- VIZORQUEIQEFRT-UHFFFAOYSA-N Diethyl adipate Chemical compound CCOC(=O)CCCCC(=O)OCC VIZORQUEIQEFRT-UHFFFAOYSA-N 0.000 abstract 2
- 235000011037 adipic acid Nutrition 0.000 abstract 2
- 239000001361 adipic acid Substances 0.000 abstract 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 abstract 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 abstract 2
- GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 abstract 2
- 239000000843 powder Substances 0.000 abstract 2
- NIDNOXCRFUCAKQ-UMRXKNAASA-N (1s,2r,3s,4r)-bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid Chemical compound C1[C@H]2C=C[C@@H]1[C@H](C(=O)O)[C@@H]2C(O)=O NIDNOXCRFUCAKQ-UMRXKNAASA-N 0.000 abstract 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 1
- 229930040373 Paraformaldehyde Natural products 0.000 abstract 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 abstract 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 229910021538 borax Inorganic materials 0.000 abstract 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 abstract 1
- -1 caprolactam Chemical class 0.000 abstract 1
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 239000007859 condensation product Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 abstract 1
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 150000003951 lactams Chemical class 0.000 abstract 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000003607 modifier Substances 0.000 abstract 1
- 238000000465 moulding Methods 0.000 abstract 1
- KSCKTBJJRVPGKM-UHFFFAOYSA-N octan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-].CCCCCCCC[O-] KSCKTBJJRVPGKM-UHFFFAOYSA-N 0.000 abstract 1
- 229920002866 paraformaldehyde Polymers 0.000 abstract 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 239000004328 sodium tetraborate Substances 0.000 abstract 1
- 235000010339 sodium tetraborate Nutrition 0.000 abstract 1
- 239000003381 stabilizer Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 239000004552 water soluble powder Substances 0.000 abstract 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 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
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/46—Block or graft polymers prepared by polycondensation of aldehydes or ketones on to macromolecular compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEH33890A DE1167022B (de) | 1958-07-25 | 1958-07-25 | Verfahren zur Herstellung modifizierter Melaminharz-Vorkondensate |
| DEH35663A DE1292395B (de) | 1958-07-25 | 1959-02-19 | Verfahren zur Herstellung modifizierter Melaminharz-Vorkondensate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB877670A true GB877670A (en) | 1961-09-20 |
Family
ID=25979498
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB25419/59A Expired GB877670A (en) | 1958-07-25 | 1959-07-24 | Process for the production of modified melamine resins |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3130178A (en, 2012) |
| BE (1) | BE580481A (en, 2012) |
| CH (1) | CH414163A (en, 2012) |
| DE (2) | DE1167022B (en, 2012) |
| FR (1) | FR1230883A (en, 2012) |
| GB (1) | GB877670A (en, 2012) |
| LU (1) | LU37318A1 (en, 2012) |
| NL (1) | NL241524A (en, 2012) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3261883A (en) * | 1963-01-02 | 1966-07-19 | Du Pont | Adhesives from polyisophthalamides and phenoplast or aminoplast syrups |
| DE2851760A1 (de) * | 1978-11-30 | 1980-06-12 | Cassella Ag | Melaminharz, verfahren zu seiner herstellung und seine verwendung zur herstellung von beschichteten holzwerkstoffen und schichtpresstoffen |
| USRE31366E (en) * | 1978-11-30 | 1983-08-30 | Cassella Aktiengesellschaft | Melamine resin, process for its manufacture and its use for the manufacture of coated wood-based materials and laminates |
| DE4434605A1 (de) * | 1994-09-28 | 1996-04-04 | Basf Ag | Mit alkoxylierten Polyamiden modifizierte Tränkharze |
| CN112175156A (zh) * | 2020-09-28 | 2021-01-05 | 安徽弘源化工科技有限公司 | 一种水基三聚氰胺树脂及其制备方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB506393A (en) * | 1937-11-25 | 1939-05-25 | Wilfred William Groves | Manufacture of resinous condensation products |
| US2317181A (en) * | 1939-08-09 | 1943-04-20 | Gen Electric | Urea-formaldehyde-triethanolamine hydrochloride condensation product |
| US2377866A (en) * | 1940-08-02 | 1945-06-12 | Gen Electric | Aminoplasts having intercondensed therein a partial amide of a polycarboxylic acid |
| DE927174C (de) * | 1941-08-03 | 1955-05-02 | Aeg | Verfahren zur Herstellung harzartiger, haertbarer Kondensationsprodukte |
| US2340046A (en) * | 1941-08-30 | 1944-01-25 | Gen Electric | Condensation product and process of making the same |
| US2340045A (en) * | 1941-08-30 | 1944-01-25 | Gen Electric | Condensation product and process of making the same |
| GB572245A (en) * | 1942-10-21 | 1945-09-28 | Du Pont | Improvements in or relating to the production of moulding powders |
| US2584177A (en) * | 1948-04-19 | 1952-02-05 | American Cyanamid Co | Modified aminoplasts and products prepared therefrom |
| AT172666B (de) * | 1948-04-19 | 1952-10-10 | American Cyanamid Co | Verfahren zur Herstellung von modifizierten synthetischen Harzen, insbesondere Aminoplasten |
| US2589567A (en) * | 1948-09-10 | 1952-03-18 | Bell & Richardson Inc De | Melamine formaldehyde scratch resistant coating composition, method of applying, and article produced thereby |
| DE1034857B (de) * | 1952-11-28 | 1958-07-24 | Rohm & Haas | Verfahren zur Herstellung methylolierter Derivate von Polyureidopolyamiden |
-
0
- NL NL241524D patent/NL241524A/xx unknown
- BE BE580481D patent/BE580481A/xx unknown
- LU LU37318D patent/LU37318A1/xx unknown
-
1958
- 1958-07-25 DE DEH33890A patent/DE1167022B/de active Pending
-
1959
- 1959-02-19 DE DEH35663A patent/DE1292395B/de active Pending
- 1959-05-26 CH CH7361059A patent/CH414163A/de unknown
- 1959-07-21 US US828458A patent/US3130178A/en not_active Expired - Lifetime
- 1959-07-21 FR FR800677A patent/FR1230883A/fr not_active Expired
- 1959-07-24 GB GB25419/59A patent/GB877670A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR1230883A (fr) | 1960-09-20 |
| NL241524A (en, 2012) | |
| LU37318A1 (en, 2012) | |
| CH414163A (de) | 1966-05-31 |
| DE1167022B (de) | 1964-04-02 |
| BE580481A (en, 2012) | |
| DE1292395B (de) | 1969-04-10 |
| US3130178A (en) | 1964-04-21 |
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