CH228438A - Method of manufacturing a paint. - Google Patents
Method of manufacturing a paint.Info
- Publication number
- CH228438A CH228438A CH228438DA CH228438A CH 228438 A CH228438 A CH 228438A CH 228438D A CH228438D A CH 228438DA CH 228438 A CH228438 A CH 228438A
- Authority
- CH
- Switzerland
- Prior art keywords
- esterified
- binding agent
- rubber
- binder
- acids
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 239000003973 paint Substances 0.000 title description 8
- 239000011230 binding agent Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 6
- 239000000194 fatty acid Substances 0.000 claims description 6
- 229930195729 fatty acid Natural products 0.000 claims description 6
- 229920000180 alkyd Polymers 0.000 claims description 5
- 150000004665 fatty acids Chemical class 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 4
- 150000007513 acids Chemical class 0.000 claims description 4
- 230000032050 esterification Effects 0.000 claims description 4
- 238000005886 esterification reaction Methods 0.000 claims description 4
- 150000005846 sugar alcohols Polymers 0.000 claims description 4
- 239000003925 fat Substances 0.000 claims description 2
- 229920005989 resin Polymers 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims description 2
- 239000007858 starting material Substances 0.000 claims description 2
- 239000010775 animal oil Substances 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 235000019197 fats Nutrition 0.000 claims 1
- 229920000515 polycarbonate Polymers 0.000 claims 1
- 239000004417 polycarbonate Substances 0.000 claims 1
- 235000015112 vegetable and seed oil Nutrition 0.000 claims 1
- 235000019871 vegetable fat Nutrition 0.000 claims 1
- 239000008158 vegetable oil Substances 0.000 claims 1
- 239000003921 oil Substances 0.000 description 13
- 235000019198 oils Nutrition 0.000 description 13
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- 239000000944 linseed oil Substances 0.000 description 7
- 235000021388 linseed oil Nutrition 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 5
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 3
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000015096 spirit Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 239000004859 Copal Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 241000782205 Guibourtia conjugata Species 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 235000004347 Perilla Nutrition 0.000 description 1
- 244000124853 Perilla frutescens Species 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229940091181 aconitic acid Drugs 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- -1 benzoyl peroside Chemical class 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000001055 chewing effect Effects 0.000 description 1
- GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 150000001869 cobalt compounds Chemical class 0.000 description 1
- IFSWBZCGMGEHLE-UHFFFAOYSA-L cobalt(2+);naphthalene-2-carboxylate Chemical compound [Co+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 IFSWBZCGMGEHLE-UHFFFAOYSA-L 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/30—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
- C08C19/34—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with oxygen or oxygen-containing groups
- C08C19/36—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with oxygen or oxygen-containing groups with carboxy radicals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/46—Polyesters chemically modified by esterification
-
- 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
- C09D115/00—Coating compositions based on rubber derivatives
-
- 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
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
-
- 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
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/08—Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Paints Or Removers (AREA)
Description
Verfahren zur Herstellung eines Anstriehmittels. Gegenstand der Erfirndüng ist ein Ver fahren zur Herstellung eines Anstrichmittels, das als Bindemittel ein aus Kautschuk her- gestelltes Produkt enthält.
Kautschuk wird in der Farben- und Lack industrie in steigendem Masse gebraucht, zwar nicht alls :solcher, doch in modifizierter Form.. Da)s wichtib to Erzeugnis ist der Chlorkautschuk, während ogyd'erter Kmt- schuk weniger Anwendung findet.
Kautschuk ergibt in gelöster Form nach Verdunstung des, Lösemittels einen Film, dem, lacktechnisch betrachtet, wenig Bedeu tung zukommt.
Es wurde nun gefunden" dass ein Reak tionsprodukt: von gegebenenfalls plastifizier- tem, depolymedsierte,m Kautschuk, mit Polyearbonsäuren, die eine aktsvet Doppel- bindung enthalten, wie Maleinsäure oder deren;
AnhydTid, Akonitsäure, Itakonsäure usw., das anschliessend einer Veresterurng mit ,einem Polyalkohol, wie Glycerol, Sorbitol, Mannitol, Pentaerythrit, Polyglycerol oder einem :schon teilweise veresterten Poly- alkoh ol., unterworfen wurde, als:
Binde- mitte#l für Lacke und Farben verwendet wer ,den kann, das diesen ,sehr günstige Eigen schaften erteilt.
Die DepolymeTisierung des Kautschuks kann nach der in der Kautschukindustrie üblichen Weise, durch Walzen bis zur Errei- chung der gewünschten Konsistenz, oder durch .einen Zusatz von geeigneten Stoffen zu einer Kautschuklösung erfolgt sein.
Als s,olehe Stoffe kommen Metallverbindungen, wie die Kobaltverbindungen von Leinölfett- sä.ure, Harzsäure oder Naplhtensäure,,die. ent- sprechenden Blei-, Kupfer- oder Mangan- er -gen und Jergl ichen,
oder auch or- v -bindun ei ganische Peroxyde, wie Benzoylperosyd, in Betracht.
Dis Vere@sterung wird zweckmässig durch geführt in Gegenwart von einem oder mehre ren der nachfolgenden Stoffe: a) Pflanzliche oder tierische Fette oder Öle, insb.eeandere trocknende oder halbtrock nende Ö:le, wie Leinöl, Sojaöl, Holzöl, Oiti- eieaöl, Tran, Perillaöl, Synourynöl (dehydra- tiertes Rizinusöl) oder deren Standöle;
<I>b)</I> Fettsäuren der unter <I>a)</I> genannten Öle, somit Harzsäure (Kolophonium oder ansge:sehmolzenes Kopal) und T'a.llöl; e) Ausgangsstoffe zur Herstellung von Alkydha.rz oder modifizierte Alkydharze, zum Beispiel ein gemischtes Glycerid von Phtalsäure und Leinölfettsäure oder andere Fettsäuren oder Harzsäuren;
d) Kunstharze, die Ester enthalten, zum Beispiel ein, mit Harzester modifiziertes Phenolformnald@e-hydha@rz.
Die gebildeten Erzeugnisse zeigen laek- technise:h überrasehend gute Eigenschaften. Die Trocknung ist schnell, ohne Na.ch- klebung, die Filme sind hart und doch elastisch, und die W asserbeIständigkeit ist gross.
Die naehatehenden Beispiele, erläutern die Herst@e,ll;un,g der .erfindungsgemässe zu ver wendenden Bindlemittel sowie der Anstrich- mittel aus diesen.
Beispiele: 1. PlastifizieTter Kautschuk wird in Lackbenzin gelöst und mit 5 % Benzoyl- peroxyd und 20% Ma.leinsäureanhydrid (be rechnet auf die Kautschukmenge) während 24 Stunden auf 100 C erhitzt.. Danach wird ,die berechnete Menge, Glycerol zugegeben und unter Rühren weiter erhitzt biss das Lackbenzin destilliert.
So viel Lackbenzin wird abdestilliert bis der Rückstand, nach Abkühlung, eine Vislros.ität von 2 Poisen be sitzt. Nun wird' so vie!1, Titanwe:iss zugegeben, da.ss eine atreiehfähige Farbe entstehen kann und die Mischung in einer Kugelmühle ge mahlen.
Das Erzeugnis trocknet in ungefähr 30 Minuten zu einem nicht klebenden Film, .der eine gute Ad@häiion, Elastizität und Wasserbeständigkeit zeigt.
2. Ein Erzeugnis nach Beispiel 1 wird, bevor die Veresterung mit Glycerol : durch geführt wird, gemischt mit Leinöl tandöl in einem Verhältnis von einem Teil Kautäch nk auf 4 Teilen Leinölsta.ndöl. Anstatt Le_nöl- standöl. kann Synouryns:tandöl oder e-n Ge misch von Leinölstandöl mit Holzölata.ndöl gebraucht werden.
Nachdem das 0l zugesetzt ist, wird die Veresterung nach der in Beispiel 1 angegebe nen Weise durchgeführt, das heisst so vi:?l Lackbenzin wird abdestilliert bis der Rück stand nach Abkühlung die Iiou::'stenz eines normalen Lackes zeigt. Der Riickstand wird sikkativiert mit so viel Kobaltnaphtenat, dass, auf -die ni:chtflü;elrtige Substanz berechnet. 0,05 % Kobalimütall vorhanden ist..
Nun würden Pigmente zugegeben und: die Mi- schung gemahlen.
Die Erzeu-nisse trocknen innerhalb 6 Stunden zu einem Film, der nach abermals 6 Stunden klebefrei und hart ist und eine gute @@'aisserbü@tändigkeit zeigt.
3. Kautschuk wird. in Sol.ventnapht:a ge löst und nach @u@,abe von ein wenig Kobalt naphtena.t: während 6 Stunden auf 80 C er hitzt. Sodann -erden<B>30%</B> Akonitsä.uTe (be- m:ehnet auf den Kautschuk) zugesetzt und unter Rühren während 48 Stunden weiter auf 80 C erhitzt.
Danach -ibt man ein mit Leinöl modifizierter Kunstharz zu, das sieh aus i'0'@ö F.ettsäuregly cerid und<B>30%</B> Phtal- säurüglvcerid zusammensetzt. Die, Menge Alkydharz kann wechseln zwischen 2-6 Teilen auf 1 Teil Kautschuk.
Dass. Gemisch wird weiter verarbeitet wie in Beispiel 2 beschrieben.
Das Produkt er-ibt einen Film von hoher Elastizität und Z@Tass rbeständigheit. Die Wasserbeständigkeit und Härte- können noch erhöht werden durch Einbrennen des Filmes auf 11.0 C %vä,hrend einür Stunde. Die Elasti zität leidet nur wenig darunter.
Process for producing a paint. The subject of the invention is a process for the production of a paint containing a product made from rubber as a binder.
Rubber is used to an increasing extent in the paint and varnish industry, not all of it: such, but in a modified form .. The most important product is chlorinated rubber, while conventional rubber is less used.
In dissolved form, after evaporation of the solvent, rubber produces a film that is of little importance from the point of view of paint technology.
It has now been found that a reaction product: of optionally plasticized, depolymerized, m rubber, with polyearboxylic acids which contain an actsvet double bond, such as maleic acid or its;
Anhydride, aconitic acid, itaconic acid, etc., which was then esterified with a polyalcohol such as glycerol, sorbitol, mannitol, pentaerythritol, polyglycerol or an already partially esterified polyalcohol, as:
Binding agent # l is used for lacquers and paints who can give them very favorable properties.
The rubber can be depolymerized in the manner customary in the rubber industry, by rolling until the desired consistency is achieved, or by adding suitable substances to a rubber solution.
Metal compounds, such as the cobalt compounds of linseed oil fatty acid, resin acid or naphthenic acid, are used as oleic substances. Corresponding lead, copper or manganese genes and days,
or or- v -bindun egg ganic peroxides, such as benzoyl peroside, into consideration.
The esterification is best carried out in the presence of one or more of the following substances: a) Vegetable or animal fats or oils, in particular other drying or semi-drying oils, such as linseed oil, soybean oil, wood oil, oitia oil, Tran, perilla oil, synouryn oil (dehydrated castor oil) or their stand oils;
<I> b) </I> fatty acids of the oils mentioned under <I> a) </I>, thus resin acid (rosin or otherwise: molten copal) and t'a.ll oil; e) Starting materials for the production of alkyd resins or modified alkyd resins, for example a mixed glyceride of phthalic acid and linseed oil fatty acid or other fatty acids or resin acids;
d) Synthetic resins containing esters, for example a phenolformnald @ e-hydha @ rz modified with rosin ester.
The products formed show laek- technise: h surprisingly good properties. Drying is fast, without sticking, the films are hard and yet elastic, and the water resistance is high.
The following examples explain the manufacture of the binders to be used according to the invention and the paints made from them.
Examples: 1. Plasticized rubber is dissolved in white spirit and heated to 100 ° C. for 24 hours with 5% benzoyl peroxide and 20% maleic acid anhydride (calculated on the amount of rubber). Then the calculated amount of glycerol is added and below Stirring continued to heat until the mineral spirits distilled.
So much white spirit is distilled off until the residue, after cooling, has a viscosity of 2 poises. Now as much as 1, titanium white is added that a breathable color can arise and the mixture is ground in a ball mill.
The product dries to a non-sticky film in about 30 minutes, which exhibits good adhesion, elasticity and water resistance.
2. Before the esterification with glycerol: is carried out, a product according to Example 1 is mixed with linseed oil in a ratio of one part of chewing oil to 4 parts of linseed oil. Instead of le_nöl stand oil. Synouryns: tandöl or a mixture of linseed oil stand oil with Holzölata.ndöl can be used.
After the oil has been added, the esterification is carried out in the manner indicated in Example 1, that is to say as much as 1 liter of mineral spirits is distilled off until the residue, after cooling, shows the consistency of a normal paint. The residue is siccativated with so much cobalt naphtenate that the non-volatile substance is calculated. 0.05% cobali metal is present.
Pigments would now be added and: the mixture would be ground.
The products dry within 6 hours to form a film which is tack-free and hard again after 6 hours and shows good resistance to scratches.
3. Rubber will. in Sol.ventnapht: a dissolved and after @ u @, but with a little cobalt naphtena.t: it is heated to 80 C for 6 hours. Then <B> 30% </B> Akonitsä.uTe (added to the rubber) are added and the mixture is further heated to 80 C for 48 hours while stirring.
Then a synthetic resin modified with linseed oil is added, which is composed of 10% fatty acid glyceride and <B> 30% </B> phthalic acid glyceride. The amount of alkyd resin can change between 2-6 parts to 1 part rubber.
That. The mixture is processed further as described in Example 2.
The product has a film of high elasticity and resistance to Z @ Tass. The water resistance and hardness can be increased by stoving the film to 11.0 C% for one hour. The elasticity suffers only a little.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL877070X | 1940-11-18 | ||
| NL228438X | 1940-11-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH228438A true CH228438A (en) | 1943-08-31 |
Family
ID=32716485
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH228438D CH228438A (en) | 1940-11-18 | 1941-10-14 | Method of manufacturing a paint. |
Country Status (2)
| Country | Link |
|---|---|
| CH (1) | CH228438A (en) |
| NL (1) | NL52884C (en) |
-
0
- NL NL52884D patent/NL52884C/xx active
-
1941
- 1941-10-14 CH CH228438D patent/CH228438A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL52884C (en) |
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