DE1081659B - Thermoplastic masses - Google Patents
Thermoplastic massesInfo
- Publication number
- DE1081659B DE1081659B DEB45397A DEB0045397A DE1081659B DE 1081659 B DE1081659 B DE 1081659B DE B45397 A DEB45397 A DE B45397A DE B0045397 A DEB0045397 A DE B0045397A DE 1081659 B DE1081659 B DE 1081659B
- Authority
- DE
- Germany
- Prior art keywords
- parts
- vinyl
- polymer
- mixed
- copolymers
- 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
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/08—Homopolymers or copolymers of vinylidene chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/003—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
Description
Viele Kunststoffe müssen vor dem Verarbeiten oder zur Erzielung bestimmter Materialeigenschaften weichgemacht werden. Ein Nachteil der üblichen niedrigmolekularen Weichmacher ist einmal deren Flüchtigkeit, so daß die weichgemachten Kunststoffe daher leicht verspröden, außerdem sind sie häufig in organischen Lösungsmitteln löslich. Verwendet man weichgemachte Folien als Verpackungsmaterial, so kann der Weichmacher auch in das Füllgut abwandern; dies ist aus hygienischen Gründen aber unerwünscht.Many plastics have to be plasticized before processing or in order to achieve certain material properties will. One disadvantage of the usual low molecular weight plasticizers is their volatility, so that the plasticized plastics therefore easily become brittle, and they are often organic Solvents soluble. If plasticized films are used as packaging material, the plasticizer can also migrate into the contents; however, this is undesirable for hygienic reasons.
Es ist bekannt, daß man die Polymerisate der höheren Acrylester als Weichmacher verwenden kann. Diese haben jedoch den Nachteil, daß sie nur beschränkt mit Kunststoffen verträglich sind und deshalb nur in geringer Menge zugesetzt werden können. Sollen die mit Acrylestern weichgemachten Kunststoffe als Lackrohstoffe verwendet werden, so haben sie ferner den Nachteil, daß sie in den üblichen Lacklösungsmitteln nicht einwandfrei löslich sind.It is known that the polymers of the higher acrylic esters can be used as plasticizers. Have this however, the disadvantage that they are only limited with plastics are compatible and can therefore only be added in small amounts. Should those with acrylic esters Plasticized plastics are used as paint raw materials, they also have the disadvantage that they are in the common paint solvents are not perfectly soluble.
Es wurde nun gefunden, daß thermoplastische Massen besonders wertvolle mechanische Eigenschaften und gute Löslichkeit haben, wenn man sie mit einem Mischpolymerisat aus 80 bis 99% eines polymerisierbaren Esters mit einer Kohlenstoffdoppelbindung und 20 bis 1 % eines N-Vinyllactams mischt.It has now been found that thermoplastic compositions have particularly valuable and good mechanical properties Have solubility if you have them with a copolymer of 80 to 99% of a polymerizable Mixes esters with a carbon double bond and 20 to 1% of an N-vinyl lactam.
Als hochmolekulare Weichmacher für spröde Kunststoffe sind besonders die Mischpolymerisate solcher Acryl- oder Methacrylsäureester und Vinylester geeignet, die für sich allein weiche Polymerisate liefern, also z. B. die Methyl-, Äthyl-, Butyl- oder Dodecylester der Acrylsäure, die Äthyl- und Butylester der Methacrylsäure oder Vinylpropionat, Vinylbutyrat. Geeignete Vinyllactame sind z. B. N-Vinylpyrrolidon, N-Vinyl-e-caprolactam und N-Vinyl-co-capryllactam. Aber auch andere Vinylverbindungen,wie Styrol, Vinyläther, Vinylchlorid, Vinylmethylketon, können in gewissem Umfang zusätzlich einpolymerisiert werden.As high molecular weight plasticizers for brittle plastics, the copolymers of such acrylic or methacrylic acid esters and vinyl esters suitable, which provide soft polymers on their own, so z. B. the Methyl, ethyl, butyl or dodecyl esters of acrylic acid, the ethyl and butyl esters of methacrylic acid or vinyl propionate, Vinyl butyrate. Suitable vinyl lactams are e.g. B. N-vinylpyrrolidone, N-vinyl-e-caprolactam and N-vinyl-co-capryllactam. But also other vinyl compounds, such as Styrene, vinyl ether, vinyl chloride, vinyl methyl ketone, can be added to some extent are polymerized.
Die Menge des Vinyllactams in den Mischpolymerisaten soll 1 bis 20 °/0, vorzugsweise S bis 10 °/0, bezogen auf das Gemisch des Ansatzes des Mischpolymerisates, betragen.The amount of vinyl lactam in the copolymers should be 1 to 20 ° / 0 , preferably 5 to 10 ° / 0 , based on the mixture of the batch of the copolymer.
Der Polymerisationsgrad der Mischpolymerisate kann entsprechend dem Verwendungszweck eingestellt werden. Kommt es nur auf die Verbesserung der Verarbeitbarkeit oder auf die weichmachende Wirkung an, so verwendet man verhältnismäßig niedermolekulare Polymerisate mit einem K-Wert (nach Fikentscher) von 20 bis 30. SoE das Mischpolymerisat dem Endprodukt auch eine zusätzliche Festigkeit verleihen, so sind höherrnolekulare Produkte mit K-Werten zwischen 60 und 80 oder höher von Vorteil. Die Einstellung des günstigsten Molekulargewichtes kann in bekannter Weise durch Variation der Polymerisationsbedingungen vorgenommen werden.The degree of polymerization of the copolymers can be adjusted according to the intended use. If it is only a matter of improving the processability or the softening effect, use it relatively low molecular weight polymers with a K value (according to Fikentscher) of 20 to 30. SoE If the copolymer also gives the end product additional strength, higher molecular weight Products with K values between 60 and 80 or higher are an advantage. The setting of the most favorable molecular weight can be carried out in a known manner by varying the polymerization conditions.
Die genannten Mischpolymerisate können nach den üblichen Polymerisationsmethoden durch Polymerisation Thermoplastische MassenThe copolymers mentioned can be polymerized by customary polymerization methods Thermoplastic masses
Anmelder:Applicant:
Badische Anilin- & Soda-FabrikAniline & Soda Factory in Baden
Aktiengesellschaft,Corporation,
Ludwigshafen/RheinLudwigshafen / Rhine
Dr. Hans Fikentscher, Bad Dürkheim,Dr. Hans Fikentscher, Bad Dürkheim,
und Dr. Karl Herrle, Ludwigshafen/Rhein,and Dr. Karl Herrle, Ludwigshafen / Rhine,
sind als Erfinder genannt wordenhave been named as inventors
im Block, in Lösung, in Emulsion oder in Suspension hergestellt werden. Bei der Polymerisation im Block setzt man geeignete Regler zu, um die stürmische Reaktion zu bremsen. Dabeiist es möglich, Polymerisate mit K-Werten unter 15 herzustellen.can be produced in block, in solution, in emulsion or in suspension. When polymerizing in the block sets one suitable regulator to slow down the stormy reaction. It is possible to use polymers with K values under 15 to manufacture.
Die genannten Mischpolymerisate besitzen eine ausgezeichnete Löslichkeit. Außer in Aromaten, Estern oder Ketonen sind sie auch in einfachen Alkoholen und je nach Zusammensetzung auch in Benzinkohlenwasserstoffen löslich. Mit zahlreichen Kunststoffen und Bindemitteln sind sie verträglich, z. B. mit Polyvinylchlorid und Vinylchlorid-Mischpolymerisaten, Vinylidenchlorid-Mischpolymerisaten, Celluloseestern, Alkydharzen, Harnstoffharzen. In Lacken verbessern sie wesentlich die Haftfestigkeit. Die Einarbeitung der Mischpolymerisate in andere Polymerisate kann auf verschiedene Arten erfolgen. Bei der Herstellung von Lacken werden die Komponenten gemeinsam in einem geeigneten Lösungsmittel gelöst. Zu Massen, die auf der Walze verarbeitet werden sollen, können die Mischpolymerisate direkt auf der Walze zugegeben werden. Vielfach ist es jedoch wünschenswert, die Mischung bereits vor der Verarbeitung, z. B. in den üblichen Mischern oder Knetern, vorzunehmen.The copolymers mentioned have excellent solubility. Except in aromatics, esters or They are also found in simple alcohols and depending on ketones Composition also soluble in petrol hydrocarbons. With numerous plastics and binders are they compatible, e.g. B. with polyvinyl chloride and vinyl chloride copolymers, Vinylidene chloride copolymers, cellulose esters, alkyd resins, urea resins. In paints, they significantly improve the adhesive strength. The incorporation of the copolymers into others Polymers can be made in various ways. In the manufacture of paints, the components are dissolved together in a suitable solvent. For masses that are to be processed on the roller, the copolymers can be added directly to the roller. In many cases, however, it is desirable the mixture before processing, e.g. B. in the usual mixers or kneaders.
Die Mischung kann auch bereits bei der Aufarbeitung oder Herstellung der Polymerisate erfolgen. So kann man das Mischpolymerisat zu dem Mohomerenansatz des weichzumachenden Polymerisats zugeben und polymerisiert dann, oder man mischt die Emulsion der Mischpolymerisate mit einer Polyvinylchloridemulsion, und arbeitet die Mischung nach den üblichen Methoden, z. B. durch Fällen, Trocknen oder Zerstäuben auf.Mixing can also take place during the work-up or production of the polymers. So you can add the mixed polymer to the Mohomere approach of the polymer to be plasticized and polymerize then, or the emulsion of the copolymers is mixed with a polyvinyl chloride emulsion, and the mixture works according to the usual methods, for. B. by felling, drying or atomizing.
Die Menge, in der die Mischpolymerisate anderen Polymerisaten zugesetzt werden, kann in weiten Grenzen schwanken. Bereits ein Zusatz von 1 bis 5 % verbessert die Verarbeitbarkeit von Polyvinylchlorid erheblich. Durch Einarbeiten von 10 bis 20 % eines N-Vinyllactam-The amount in which the copolymers are added to other polymers can be within wide limits vary. Even an addition of 1 to 5% improves the processability of polyvinyl chloride considerably. By incorporating 10 to 20% of an N-vinyl lactam
009 509/436009 509/436
Claims (1)
mit einem K-Wert 70 gemischt und die Mischung im80 parts of a 40% emulsion of polyvinyl chloride Patent claim
mixed with a K value of 70 and the mixture in
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEB45397A DE1081659B (en) | 1957-07-20 | 1957-07-20 | Thermoplastic masses |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEB45397A DE1081659B (en) | 1957-07-20 | 1957-07-20 | Thermoplastic masses |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1081659B true DE1081659B (en) | 1960-05-12 |
Family
ID=6967601
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEB45397A Pending DE1081659B (en) | 1957-07-20 | 1957-07-20 | Thermoplastic masses |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE1081659B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4746705A (en) * | 1985-03-15 | 1988-05-24 | Imperial Chemical Industries Plc | Vinyl chloride polymer composition containing (meth)acrylate-alpha methyl styrene copolymer |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE757355C (en) * | 1939-08-02 | 1953-11-02 | Ig Farbenindustrie Ag | Process for the preparation of polymerization products |
-
1957
- 1957-07-20 DE DEB45397A patent/DE1081659B/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE757355C (en) * | 1939-08-02 | 1953-11-02 | Ig Farbenindustrie Ag | Process for the preparation of polymerization products |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4746705A (en) * | 1985-03-15 | 1988-05-24 | Imperial Chemical Industries Plc | Vinyl chloride polymer composition containing (meth)acrylate-alpha methyl styrene copolymer |
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