PL80608B1 - - Google Patents
Download PDFInfo
- Publication number
- PL80608B1 PL80608B1 PL13892170A PL13892170A PL80608B1 PL 80608 B1 PL80608 B1 PL 80608B1 PL 13892170 A PL13892170 A PL 13892170A PL 13892170 A PL13892170 A PL 13892170A PL 80608 B1 PL80608 B1 PL 80608B1
- Authority
- PL
- Poland
- Prior art keywords
- melamine
- urea
- resins
- formaldehyde
- glycol
- Prior art date
Links
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 50
- 229920000877 Melamine resin Polymers 0.000 claims description 25
- 239000003607 modifier Substances 0.000 claims description 24
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 19
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 16
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 239000004202 carbamide Substances 0.000 claims description 9
- -1 amino, imino Chemical group 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 7
- 150000005846 sugar alcohols Polymers 0.000 claims description 7
- 229930040373 Paraformaldehyde Natural products 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 125000003368 amide group Chemical group 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 229920002866 paraformaldehyde Polymers 0.000 claims description 6
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 6
- 150000002466 imines Chemical class 0.000 claims description 5
- 150000007513 acids Chemical class 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 4
- 239000007859 condensation product Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 claims description 3
- 150000001299 aldehydes Chemical class 0.000 claims description 3
- 150000001414 amino alcohols Chemical class 0.000 claims description 3
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims description 2
- 239000011356 non-aqueous organic solvent Substances 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 230000001476 alcoholic effect Effects 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 38
- 229920005989 resin Polymers 0.000 description 25
- 239000011347 resin Substances 0.000 description 25
- 239000000243 solution Substances 0.000 description 24
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 19
- 235000019256 formaldehyde Nutrition 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 8
- 238000003825 pressing Methods 0.000 description 8
- 239000000047 product Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- 239000004640 Melamine resin Substances 0.000 description 4
- 235000011037 adipic acid Nutrition 0.000 description 4
- 239000001361 adipic acid Substances 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229920003180 amino resin Polymers 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000011093 chipboard Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 125000001841 imino group Chemical group [H]N=* 0.000 description 2
- 239000002648 laminated material Substances 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical class Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical compound NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 description 1
- NJYZCEFQAIUHSD-UHFFFAOYSA-N acetoguanamine Chemical compound CC1=NC(N)=NC(N)=N1 NJYZCEFQAIUHSD-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- QWJNFFYFEKXZBF-UHFFFAOYSA-N cyanocyanamide Chemical compound N#CNC#N QWJNFFYFEKXZBF-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000003827 glycol group Chemical group 0.000 description 1
- 150000002402 hexoses Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000002972 pentoses Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 230000003678 scratch resistant effect Effects 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000008096 xylene Substances 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
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
-
- 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
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
- C08G12/04—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
- C08G12/10—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with acyclic compounds having the moiety X=C(—N<)2 in which X is O, S or —N
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 (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT189869A AT295142B (de) | 1969-02-25 | 1969-02-25 | Verfahren zur Herstellung von Modifikatoren für Carbamidharze |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL80608B1 true PL80608B1 (en, 2012) | 1975-08-30 |
Family
ID=3523398
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL13892170A PL80608B1 (en, 2012) | 1969-02-25 | 1970-02-20 |
Country Status (7)
| Country | Link |
|---|---|
| AT (1) | AT295142B (en, 2012) |
| CH (1) | CH537431A (en, 2012) |
| DE (1) | DE1932523A1 (en, 2012) |
| FR (1) | FR2032379A1 (en, 2012) |
| GB (1) | GB1284280A (en, 2012) |
| PL (1) | PL80608B1 (en, 2012) |
| RO (1) | RO56457A (en, 2012) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3959201A (en) | 1972-10-26 | 1976-05-25 | Ppg Industries, Inc. | High solids, water thinnable compositions |
| GB1603431A (en) * | 1977-05-24 | 1981-11-25 | British Industrial Plastics | Resin manufacture |
| DE2824473A1 (de) * | 1978-06-03 | 1979-12-06 | Cassella Ag | Melaminharze und verfahren zu ihrer herstellung |
| DE3043616A1 (de) * | 1980-11-19 | 1982-07-01 | Basf Ag, 6700 Ludwigshafen | Mittel zur modifizierung von aminoplastharzen und verfahren zu seiner herstellung |
| DE3044151A1 (de) | 1980-11-24 | 1982-06-24 | Lentia GmbH Chem. u. pharm. Erzeugnisse - Industriebedarf, 8000 München | Modifizierte aminoplaste |
| DE3735956A1 (de) * | 1987-10-23 | 1989-05-03 | Kopp Gmbh & Co Kg Heinrich | Optisches richtmittel fuer infrarot-bewegungsmelder, punktleuchten u. dgl. |
| DE19800553C2 (de) * | 1997-01-18 | 2003-07-31 | Leuze Electronic Gmbh & Co | Optoelektronische Vorrichtung |
-
1969
- 1969-02-25 AT AT189869A patent/AT295142B/de not_active IP Right Cessation
- 1969-06-26 DE DE19691932523 patent/DE1932523A1/de active Pending
- 1969-07-17 FR FR6924433A patent/FR2032379A1/fr not_active Withdrawn
- 1969-08-28 GB GB4298269A patent/GB1284280A/en not_active Expired
-
1970
- 1970-02-13 CH CH208970A patent/CH537431A/de not_active IP Right Cessation
- 1970-02-20 PL PL13892170A patent/PL80608B1/pl unknown
- 1970-02-24 RO RO6254770A patent/RO56457A/ro unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB1284280A (en) | 1972-08-02 |
| CH537431A (de) | 1973-05-31 |
| RO56457A (en, 2012) | 1974-09-01 |
| FR2032379A1 (en, 2012) | 1970-11-27 |
| AT295142B (de) | 1971-12-27 |
| DE1932523A1 (de) | 1970-09-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0530783B1 (en) | Latent catalysts | |
| US2528359A (en) | Polyepoxide-containing compositions and reaction products | |
| US8460758B2 (en) | Process for the preparation of a crosslinker composition | |
| US9039927B2 (en) | Etherified melamine/formaldehyde condensates having a high solid content and low viscosity | |
| US3293324A (en) | 2-dimethylamino-2-methyl-1-propanol-p-toluene sulfonate with urea-formal-dehyde resin and alkyd resin | |
| US2524727A (en) | Reaction products of an aldehyde and a triazine derivative | |
| PL80608B1 (en, 2012) | ||
| US4081426A (en) | Preparation of aminoplasts | |
| EP2621975B1 (en) | Process for the preparation of a reaction product of a cyclic urea and a multifunctional aldehyde | |
| JP6531136B2 (ja) | 修飾アミノ樹脂 | |
| US3654229A (en) | Baking enamel vehicle comprising the reaction product of an oxazoline with melamine and formaldehyde | |
| US2481155A (en) | Resinous compositions | |
| TWI516514B (zh) | 環狀脲與多官能性醛之未醚化的反應產物 | |
| US2218077A (en) | Resinous condensation products and process of making same | |
| US2508875A (en) | Modified melamine resins | |
| US2851429A (en) | Combination of aminoplast resins and certain alkyd resins | |
| US3130178A (en) | Process for the preparation of modified melamine resins | |
| US2665260A (en) | Preparation of infusible resins of superior toughness and flexibility from a ketodiguanamine and formaldehyde | |
| US3371067A (en) | Melamine-formaldehyde-acrylonitrile condensation product and process of making same | |
| US6355794B1 (en) | Lactam derivatives for melamine impregnating resins, and resin mixtures containing them | |
| EP0391665A1 (en) | Amino compounds, amino resins obtained therefrom, production of amino resins and resin compositions for water-borne coatings | |
| RU2026309C1 (ru) | Способ получения модифицированных аминоформальдегидных смол | |
| US3152095A (en) | Mixed normal salts of maleic acid and their catalystic use in aminoplast resin compositions | |
| US2640043A (en) | Phenol-aldehyde-ketone resins | |
| GB608186A (en) | Method of preparing guanamine-aldehyde condensation products |