CH198970A - Process for the production of paints. - Google Patents
Process for the production of paints.Info
- Publication number
- CH198970A CH198970A CH198970DA CH198970A CH 198970 A CH198970 A CH 198970A CH 198970D A CH198970D A CH 198970DA CH 198970 A CH198970 A CH 198970A
- Authority
- CH
- Switzerland
- Prior art keywords
- parts
- volume
- weight
- paints
- production
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 238000000034 method Methods 0.000 title claims description 4
- 239000003973 paint Substances 0.000 title description 7
- QQOWHRYOXYEMTL-UHFFFAOYSA-N triazin-4-amine Chemical class N=C1C=CN=NN1 QQOWHRYOXYEMTL-UHFFFAOYSA-N 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 239000002966 varnish Substances 0.000 claims description 3
- 238000006356 dehydrogenation reaction Methods 0.000 claims 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 19
- 239000000243 solution Substances 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 239000007859 condensation product Substances 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 229920000877 Melamine resin Polymers 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 5
- 239000004922 lacquer Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000000020 Nitrocellulose Substances 0.000 description 3
- 230000001476 alcoholic effect Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920001220 nitrocellulos Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- -1 methylol compounds Chemical class 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 1
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D161/00—Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
- C09D161/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C09D161/26—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Description
Verfahren zur Rerstellung von Laeken. Gegenstand vorliegender Erfindung ist ein Verfahren zur Herstellung von Lack-en, .dadurch gekennzeichnet, dass man als lack bildende Substanz Formal!d.ehydkon#densa.- tionsprodukte von Aminotriazinen verwendet.
Dieerhaltenen Lacke besitzen die Eigen schaft, Überzüge zu liefern, die einerseits, in ,der Hitze, hart und unlöslich werden und<B>an-</B> derseits lichtbestänci-ig und frei von Eigen- farbe,sind.
Die Reaktion zwischen Forma-Idehyd und Aminotriazinen, insbesondere Melamin, er- lolgt in mehreren Stufen. Zunächst werden Methylolverbindungen gebildet,die in Wasser und Alkohol beliebig löslich, sind. Bei Weiter- f Ührung der Kondensation bilden sieh zu- näch-st hyd#ropllile, dann hydrophobe, Harze.
D#uroli Hitzebehandlung gehendie Kondensa tionsprodukte schliesslich in harte, unlösliche und unsellmelzbare Massen über.
Als besonders geeignet haben sieh ,clie Formaldehydkondensationsprodukte des 2.4.6-Tri,am#ino-I.'3.,5-tria,zins erwiesen. Doch können auch- Formald#ehydkonden(sa- tionspTodukte von andern Aininotriazinen mit Vorteil für den vorliegenden Zweck Ver wendung finden, z. B. 2. 4-Amino-l. <B>3.</B> 5- triazin (Formoguanamin) und Jergl.
Zur Überführung in Lacke werden die Kondensationsprodukte vorzugsweise, in orga- nisellen Lösungsmitteln, wie z. B. Ilhyl- alkoliol, ButylaJkoliol oder Glyzeriden der Leinölsäure, gelöst. Man kann auch die Kon- densationsprodukte in Gegenwart organischer Lösungsmittel herstellen. Ineliesem Falle ent stehen direkt Lösungen, die zux Herstellung von Lacken, z.
B. Nitrozelluloselacken,dienen können. Doch können auch wässerige, Lösun gen der Kondensationsprodukte, zur Herstel- lun#g der Lacke dienen. Die Fo#rmal#dellycl-- kondensationsprodukte der Aminotriazine können auch im Gemisch mit andern lack bildenden, Substanzen oder mit üblichen Zu sätzen verwendet werden.
<I>Beispiel<B>1:</B></I> <B>12,6</B> Gewichtsteile<B>(0,1</B> Moi) Melamin werden in<B>75</B> Volumteilen. <B>(0,8</B> Mol) 32 volum- prozentigem neutralem Formaldehyd im sie denden Wasserbad gelöst und<B>10</B> Minuten dort belassen. Hierauf wird gekühlt, wobei .sich schon beim Abkühlen Flocken aus scheiden. Nach zwei Tagen wird der Kristall brei abgenutscht, mit Alkohol gründlich ge waschen und fünf Stunden bei<B>60' C</B> getrocknet.
<B>50</B> Gewichtsteile der so erhaltenen Me- thylolverbindung des Melarnins werden zu<B>80</B> Volumteilen Butylalkohol und<B>0,5</B> Volum- teilen konzentrierter Salzsäure gegeben und '/4 Stund-e zum Sieden erhitzt. Fs entsteht eine fast klare Lösung, die einen gebrauchs fertigen Lack darstellt und in dünner Schicht in der Hitze rasch zu einem harten Lackfilin trocknet und erhärtet.
Solche Lösungen in Butylalkohol können zum Beispiel Nitro- zelluloselacken zugesetzt werden. um ihnen Härte und Füllkraft zu verleihen.
<I>Beispiel 2:</I> <B>50</B> Gewichtsteile, Nitrozellulose ("1/2"Se- kunden-Wolle") werden in einem Gemisch aus<B>10</B> Gewichtsteilen Trikre.sylphosphat, <B>10</B> Gewichtsteilen Butylalkoho#ll 50 Gewichts teilen Fssigester und 40 Gewichtsteilen Toluol gelöst.
In die erhaltene sehr dicke, pasten- förmige Lösung werden<B>100</B> Gewichtsteile, einer alkohol:ischen Melaminharzlösung ein gerührt, die durch Erhitzen von<B>126</B> Ge- wielitsteilen Melamin <B>(1</B> Mol) mit<B>360</B> Vo- lumteilen einer 41,8prozentigen alkoholischen Formaldehydlösung <B>(5</B> Mol),
<B>300</B> Volum- teilen Alkohol und<B>1</B> Volumteil konzentrierter Salzsäure, (0,01 Mol) unter Rückfluss während 45 Minuten und naellheriges Abkühlen der Lösung hergestellt worden ist. Die e#rhaJtene waisserklare Lösung wird zum Gebrauch mit einem Gemisch von gleichen Teilen Tolue,1, absolutem Alkohol und Essigester verdünnt.
Der so erhaltene Lack trocknet, auf Glas oder Metall ausgegossen, wasserhell und spiegel glatt und liefert, bei langsam steigender Temperatur gehärtet, wobei schliesslich die Temperatur zirka Y2 Stunde bei 120'<B>C</B> o-e- halten wird, Lackfilme von sehr guter Wasserbestäadigkeit und Härte.
<I>Beispiel<B>3:</B></I> Man stellt zunächst eine Harzlösung wie folgt dar:<B>6,3</B> Gewichtsteile- Melamin ('l. Mol), <B>15</B> Volumteile 41,8prozentiger al koholischer Formaldehy#d ('/. Mol), <B>15</B> Vo- lumteile absoluter Alkohol,<B>0,1</B> Volumteil konzentrierter Salzsäure ('/1"" Mol)
und<B>6</B> Ge- wieUtsteile des Monoglyzerids der Linolen- säure werden zusammen 31/2 Stunden auf ,dem gsiedenden Waisserbad am Rückfluss reagieren gelassen.
Die entstehende etwas trübe, schwach gelbliche, ölige Flüssigkeit wird vor dem Erstarren mit etwas Benzol verdünnt und zweckmässig mit einem Sikkativ versetzt. Der so erhaltene Lack trocknet, auf eine Unterlage aufgebracht, an der Luft nach einiger Zeit zu klar duxelisichtigen, harten, mit dem Nagel nicht mehr ritzbaren Über zügen auf.
Procedure for the creation of Laeken. The present invention relates to a process for producing paints, characterized in that formaldehyde condensation products of aminotriazines are used as the paint-forming substance.
The varnishes obtained have the property of providing coatings which, on the one hand, become hard and insoluble in the heat and, on the other hand, are lightfast and free of their own color.
The reaction between formaldehyde and aminotriazines, especially melamine, takes place in several stages. First, methylol compounds are formed, which are arbitrarily soluble in water and alcohol. If the condensation is continued, the next hydropillic, then hydrophobic, resins form.
D # uroli heat treatment, the condensation products finally turn into hard, insoluble and non-meltable masses.
The formaldehyde condensation products of 2.4.6-tri, am # ino-I.'3., 5-tria, zins have proven particularly suitable. However, formaldehyde condensate products of other amino triazines can also be used with advantage for the present purpose, e.g. 2,4-amino-1. 3-5-triazine (formoguanamine ) and Jergl.
For conversion into paints, the condensation products are preferably in organic solvents such as. B. Ilhylalkoliol, ButylaJkoliol or glycerides of linoleic acid, dissolved. The condensation products can also be prepared in the presence of organic solvents. Ineliesem case arise directly solutions that zux manufacture of paints, z.
B. nitrocellulose lacquers, can serve. However, aqueous solutions of the condensation products can also be used to manufacture the paints. The fo # rmal # dellycl-- condensation products of the aminotriazines can also be used in a mixture with other lacquer-forming substances or with conventional additives.
<I>Example<B>1:</B> </I> <B> 12.6 </B> parts by weight <B> (0.1 </B> Moi) melamine are in <B> 75 </ B> Volume divide. <B> (0.8 </B> Mol) 32 percent by volume neutral formaldehyde dissolved in the water bath and leave for <B> 10 </B> minutes. This is followed by cooling, with flakes separating out as soon as they cool down. After two days, the crystal pulp is sucked off, washed thoroughly with alcohol and dried for five hours at <B> 60 ° C </B>.
<B> 50 </B> parts by weight of the methylol compound of melamine thus obtained are added to <B> 80 </B> parts by volume of butyl alcohol and <B> 0.5 </B> parts by volume of concentrated hydrochloric acid and 1/4 Hour-e heated to the boil. The result is an almost clear solution, which is a ready-to-use lacquer and quickly dries in a thin layer in the heat to form a hard lacquer film and hardens.
Such solutions in butyl alcohol can be added to nitrocellulose lacquers, for example. to give them hardness and fullness.
<I> Example 2: </I> <B> 50 </B> parts by weight of nitrocellulose ("1/2" second wool ") are triked in a mixture of <B> 10 </B> parts by weight. syl phosphate, <B> 10 </B> parts by weight of butyl alcohol, 50 parts by weight of liquid ester and 40 parts by weight of toluene dissolved.
<B> 100 </B> parts by weight of an alcoholic melamine resin solution are stirred into the very thick, paste-like solution obtained, which is obtained by heating <B> 126 </B> parts by weight of melamine <B> (1 </B> Mol) with <B> 360 </B> parts by volume of a 41.8 percent alcoholic formaldehyde solution <B> (5 </B> Mol),
<B> 300 </B> parts by volume of alcohol and <B> 1 </B> part by volume of concentrated hydrochloric acid (0.01 mol) under reflux for 45 minutes and subsequent cooling of the solution. The aged white solution is diluted for use with a mixture of equal parts of toluene, 1, absolute alcohol and ethyl acetate.
The paint obtained in this way dries, poured onto glass or metal, water-white and mirror-smooth and, cured at a slowly increasing temperature, the temperature finally being kept at 120 ° C for about 2 hours, paint films of very good water resistance and hardness.
<I>Example<B>3:</B> </I> First, a resin solution is prepared as follows: <B> 6.3 </B> parts by weight melamine (1 mole), <B> 15 </B> Part by volume 41.8 percent alcoholic formaldehyde # d ('/. Mol), <B> 15 </B> part by volume absolute alcohol, <B> 0.1 </B> part by volume concentrated hydrochloric acid (' / 1 "" mole)
and <B> 6 </B> Parts of the monoglyceride of linolenic acid are allowed to react together for 31/2 hours on the refluxing Waisserbath.
The resulting somewhat cloudy, pale yellowish, oily liquid is diluted with a little benzene before it solidifies and a siccative is added to it. The varnish obtained in this way, when applied to a base, dries in the air after some time to form clear, double-sided, hard coatings that can no longer be scratched with the nail.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH198970X | 1935-09-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH198970A true CH198970A (en) | 1938-07-31 |
Family
ID=35517532
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH198970D CH198970A (en) | 1935-09-28 | 1935-09-28 | Process for the production of paints. |
Country Status (2)
| Country | Link |
|---|---|
| CH (1) | CH198970A (en) |
| NL (1) | NL45877C (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE748829C (en) * | 1939-10-17 | 1952-11-10 | Ig Farbenindustrie Ag | Stoving enamels |
-
0
- NL NL45877D patent/NL45877C/xx active
-
1935
- 1935-09-28 CH CH198970D patent/CH198970A/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE748829C (en) * | 1939-10-17 | 1952-11-10 | Ig Farbenindustrie Ag | Stoving enamels |
Also Published As
| Publication number | Publication date |
|---|---|
| NL45877C (en) | 1939-06-15 |
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