DE1235586B - Hardeners in polyester molding compounds - Google Patents
Hardeners in polyester molding compoundsInfo
- Publication number
- DE1235586B DE1235586B DE1963G0037586 DEG0037586A DE1235586B DE 1235586 B DE1235586 B DE 1235586B DE 1963G0037586 DE1963G0037586 DE 1963G0037586 DE G0037586 A DEG0037586 A DE G0037586A DE 1235586 B DE1235586 B DE 1235586B
- Authority
- DE
- Germany
- Prior art keywords
- polyester
- hardeners
- polyester molding
- molding compounds
- hydroquinone
- 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
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
- 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
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/20—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
-
- 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
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/42—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes polyesters; polyethers; polyacetals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Polymers & Plastics (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Polyesters Or Polycarbonates (AREA)
- Furan Compounds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyamides (AREA)
Description
Härter in Polyester-Formmassen Polyester-Formmassen sind Stoffgemische, die einen ungesättigten Polyester, daran anpolymerisierbare monomere Verbindungen und einen Katalysator, gegebenenfalls auch einen Beschleuniger enthalten. Erhitzt man solche Massen, dann härten sie aus.Hardeners in polyester molding compounds Polyester molding compounds are mixtures of substances the one unsaturated polyester, monomeric compounds that can be polymerized onto it and a catalyst, optionally also an accelerator. Heated you get such masses, then they harden.
Ein typischer Vertreter eines Polyesters kann bei der praktischen Durchführung der Erfindung aus den folgenden Stoffen wie üblich hergestellt werden: Dimethylterephthalat 46 Prozentäquivalente (3 Mol) Äthylenglycol ...... 31 Prozentäquivalente (2 Mol) Glycerin (95 °/o) .... 23 Prozentäquivalente (1 Mol) Die vorgenannten Verbindungen wurden zusammen mit Xylol oder einem ähnlichen Lösungsmittel, das ein Verdampfen der niederen Dialkylester der Säuren verhindert, in einen Dreihalskolben eingegeben, welcher einen Thermometer, einen Rührer und eine Vigreux-Kolonne mit einer Dean- und Stark-Vorlage und einen zusätzlichen Trichter auf der Kolonne aufwies, eingegeben. Ferner wurde bei diesem System eine Stickstoffschutzatmosphäre hergestellt. Das System wurde etwa 30 Minuten lang erhitzt, innerhalb welcher Zeitspanne die Gefäßtemperatur auf 130°C anstieg und das Wasser und das Xylol azeotropisch abdestillierten. Sodann wurden 0,03 Gewichtsprozent, bezogen auf das Gewicht des Dimethylterephthalats, an Bleiacetat als Alkoholysekatalysator zugegeben und die Erhitzung etwa weitere 31/z Stunden fortgeführt, unter Erreichung einer Endtemperatur von 240'C. Anschließend wurde der Polyester abgekühlt und zerkleinert.A typical representative of a polyester can be prepared in the practice of the invention from the following materials as usual: Dimethyl terephthalate 46 percent equivalents (3 moles) ethylene glycol ...... 31 percent equivalents (2 moles) glycerol (95%) .. .. 23 percent equivalents (1 mol) The aforementioned compounds were placed together with xylene or a similar solvent, which prevents evaporation of the lower dialkyl esters of the acids, in a three-necked flask, which has a thermometer, a stirrer and a Vigreux column with a Dean and Stark template and an additional funnel on the column. In addition, a protective nitrogen atmosphere was created in this system. The system was heated for about 30 minutes, during which time the vessel temperature rose to 130 ° C and the water and xylene distilled off azeotropically. Then 0.03 percent by weight, based on the weight of the dimethyl terephthalate, of lead acetate was added as alcoholysis catalyst and heating was continued for about a further 31/2 hours, reaching a final temperature of 240.degree. The polyester was then cooled and comminuted.
Es soll weiter betont werden, daß natürlich - wenn dies gewünscht ist - viele Variationen bei dem vorgenannten Polyester gemacht werden können. Beispielsweise können die Polyester des vorbeschriebenen Typs mit den Kondensationsprodukten oder Reaktionsprodukten anderer Polyolmaterialien oder mit anderen oder ähnlichen polybasischen Säuren oder Säurederivaten umgesetzt werden.It should also be emphasized that of course - if so desired is - many variations can be made in the aforementioned polyester. For example can the polyesters of the type described above with the condensation products or Reaction products of other polyol materials or with other or similar polybasic ones Acids or acid derivatives are implemented.
Erfindungsgegenstand ist die Verwendung von Hydrochinon-bis-trimellithsäureanhydrid als Härter in wie üblich aufgebauten Polyester-Formmassen oder -Überzugsmassen.The subject of the invention is the use of hydroquinone-bis-trimellitic anhydride as a hardener in customary polyester molding compositions or coating compositions.
In den Polyester-Formmassen gemäß dieser Erfindung wird das Hydrochinon-bis-trimellithsäureanhydrid mit dem Polyester in stöchiometrischen Mengen kombiniert.In the polyester molding compositions according to this invention, the hydroquinone-bis-trimellitic anhydride is used combined with the polyester in stoichiometric amounts.
Monomere und andere Katalysatoren sind in den Massen nicht nötig.Monomers and other catalysts are not needed in the bulk.
Eine pulverisierte Polyester-Formmasse wurde dadurch hergestellt, daß 100 Teile des oben beschriebenen bevorzugten Polyesterharzes zusammen mit 3 Teilen Titandioxyd als Pigment und 2,5 Gewichtsteilen eines thixotropen, aus der Gasphase hergestellten Silicamaterials verwendet wurden.A powdered polyester molding compound was produced by that 100 parts of the above-described preferred polyester resin together with 3 Parts of titanium dioxide as a pigment and 2.5 parts by weight of a thixotropic, from the Gas phase produced silica were used.
Beispiel Zu der vorgenannten Formmasse wurden pro 100 g Polyesterharz 21 g Hydrochinon-bis-trimellithsäureanhydrid zugegeben, welches dadurch hergestellt wurde, daß äquivalente Teile von Trimellithsäureanhydrid und Hydrochinondiacetat umgesetzt wurden, wobei diese Umsetzung hier nicht geschützt werden soll. Eine 3-g-Probe aus feingepulvertem Material der so hergestellten Masse wurde auf eine Temperatur von 197'C erhitzt, wobei festgestellt wurde, daß die benötigte Zeit zur Gelbbildung etwa 6 Minuten betrug; dieser Test wurde auf einem Sunshine-Gelatinierungsmesser durchgeführt. Wenn das gepulverte Material mit Hilfe eines Flüssigbettprozesses auf Draht aufgegeben wurde und splintartige Teilchen von derart überzogenem Draht zusammengesetzt und 10 Minuten bei 220'C gehärtet wurden, war eine Kraft von 3,5 englischen Pfund notwendig, um die splintartigen Teilchen bei 200'C auseinanderzuziehen. Die Rockwell-Härte eines Überzugs, der 1 Stunde lang bei 220°C gehärtet wurde, wurde zu 43 ermittelt. Der Rockwell-Härte-Test ist ein Maß für die Durchschneidefestigkeit bzw. für die Widerstandsfähigkeit der Überzüge gegenüber Beeinträchtigungen unter hohem Druck.EXAMPLE 100 g of polyester resin were added to the aforementioned molding material 21 g of hydroquinone-bis-trimellitic anhydride were added, which was thereby produced was that equivalent parts of trimellitic anhydride and hydroquinone diacetate were implemented, although this implementation is not to be protected here. One 3 g sample from finely powdered material of the mass produced in this way was heated to a temperature heated from 197'C, where it was found that the time required for yellowing was about 6 minutes; this test was on a Sunshine Gelatinizer carried out. When the powdered material using a fluidized bed process on wire and splint-like particles of wire coated in this way were assembled and cured for 10 minutes at 220 ° C, a force of 3.5 English pounds are necessary to pull the sapwood-like particles apart at 200'C. The Rockwell hardness of a coating that is at Hardened at 220 ° C was determined to be 43. The Rockwell Hardness Test is a measure of cut through resistance or for the resistance of the coatings to impairments high pressure.
Motorständer, die mit den Formmassen überzogen waren, besaßen dielektrische Konstanten von mehr als 2400 Volt pro Mil und zeigten auch sonst gute elektrische Überzugs- und physikalische Charakteristika.Motor stands that were coated with the molding compounds had dielectric ones Constants greater than 2400 volts per mil and also showed good electrical otherwise Coating and physical characteristics.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US19080662A | 1962-04-27 | 1962-04-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1235586B true DE1235586B (en) | 1967-03-02 |
Family
ID=22702863
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE1963G0045811 Pending DE1243387B (en) | 1962-04-27 | 1963-04-25 | Certain hardeners in polyester molding compounds |
DE1963G0037586 Pending DE1235586B (en) | 1962-04-27 | 1963-04-25 | Hardeners in polyester molding compounds |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE1963G0045811 Pending DE1243387B (en) | 1962-04-27 | 1963-04-25 | Certain hardeners in polyester molding compounds |
Country Status (4)
Country | Link |
---|---|
BE (1) | BE631375A (en) |
DE (2) | DE1243387B (en) |
FR (1) | FR1356006A (en) |
GB (1) | GB1032372A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1287309B (en) * | 1966-06-07 | 1969-01-16 | Huels Chemische Werke Ag | Manufacture of polyester molding compounds |
FR2295990A1 (en) * | 1974-12-24 | 1976-07-23 | Rhone Poulenc Ind | CROSS-LINKABLE COMPOSITIONS BASED ON SATURATED POLYESTERS |
-
0
- BE BE631375D patent/BE631375A/xx unknown
-
1963
- 1963-04-25 DE DE1963G0045811 patent/DE1243387B/en active Pending
- 1963-04-25 GB GB1638863A patent/GB1032372A/en not_active Expired
- 1963-04-25 DE DE1963G0037586 patent/DE1235586B/en active Pending
- 1963-04-26 FR FR932820A patent/FR1356006A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR1356006A (en) | 1964-03-20 |
BE631375A (en) | |
DE1243387B (en) | 1967-06-29 |
GB1032372A (en) | 1966-06-08 |
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