DE84146C - - Google Patents

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Publication number
DE84146C
DE84146C DENDAT84146D DE84146DA DE84146C DE 84146 C DE84146 C DE 84146C DE NDAT84146 D DENDAT84146 D DE NDAT84146D DE 84146D A DE84146D A DE 84146DA DE 84146 C DE84146 C DE 84146C
Authority
DE
Germany
Prior art keywords
dichlorohydrin
epichlorohydrin
chlorohydrins
amber
gives
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.)
Active
Application number
DENDAT84146D
Other languages
German (de)
Publication of DE84146C publication Critical patent/DE84146C/de
Active legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D193/00Coating compositions based on natural resins; Coating compositions based on derivatives thereof

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Chemical And Physical Treatments For Wood And The Like (AREA)
  • Paints Or Removers (AREA)

Description

KAISERLICHESIMPERIAL

PATENTAMT.PATENT OFFICE.

Bisher mufste man Bernstein und Copale zur Verwendung in der Lackfabrikation schmelzen, ehe dieselben in Leinöl und Terpentin gelöst werden konnten. Nach vorliegender Erfindung wird die Lösung der genannten Harze ohne vorgängiges Schmelzen durch die Einwirkung von Chlorhydrinen des Glycerins, insbesondere von Dichlorhydrin C3H5CL2(HOJ und Epichlorhydrin C3H5 O Cl herbeigeführt. > Up until now, amber and copale had to be melted for use in lacquer manufacture before they could be dissolved in linseed oil and turpentine. According to the present invention, the solution of the resins mentioned is brought about without prior melting by the action of chlorohydrins of glycerol, in particular dichlorohydrin C 3 H 5 CL 2 (HOJ and epichlorohydrin C 3 H 5 O Cl . >

Zu diesem Zwecke werden die zerkleinerten Harze mittelst Chlorhydrinen des Glycerins, insbesondere Dichlorhydrin und Epichlorhydrin, unter Erwärmung bezw. Kochen behandelt. Die Lösung kann auch unter Druck oder im luftleeren Räume bewirkt werden. Epichlorhydrin giebt hellere Lösungen als Dichlorhydrin. For this purpose the comminuted resins are mixed with the chlorohydrins of glycerine, in particular dichlorohydrin and epichlorohydrin, respectively with heating. Cooking treats. The solution can also be effected under pressure or in a vacuum. Epichlorohydrin gives lighter solutions than dichlorohydrin.

Der bedeutende, beim Schmelzen der Harze entstehende und durch das Entweichen flüchtiger OeIe begründete Gewichtsverlust wird durch das Löseverfahren vermieden. Den mit den beschriebenen Lösungen hergestellten Lackschichten bleibt der ursprüngliche Glanz, die Härte und Polirbarkeit des Rohmaterials erhalten. Die Harzsplitter, Bernstein-Drehspäne und ähnliche Abfälle, welche für die bisherige Art der Lackbereitung weit geringeren Werth hatten als die grofsen Stücke, sind für die vorliegende Erfindung mit jenen gleichwerthig. Die Chlorhydrine können zum Zwecke der Lösung mit dem in der Lackfabrikation gebräuchlichen Alkohol vermischt werden.The major one, which is produced when the resins melt and is more volatile as it escapes OeIe justified weight loss is avoided by the dissolution process. The one with the The solutions described above retain their original gloss Preserved the hardness and polishability of the raw material. The resin splinters, amber turnings and similar waste, which is of far less value for the previous type of paint preparation had as the larger pieces, are equivalent to those for the present invention. The chlorohydrins can be used to dissolve them with those commonly used in paint production Mixed with alcohol.

Beispiel:Example:

Man übergiefst 1 Theil zerkleinerten Kauri mit ι Theil Dichlorhydrin oder Epichlorhydrin, lä'fst das Gemisch einige Zeit stehen, fügt ι Theil Alkohol zu und erwärmt bis zur völligen Lösung. Nach Zusatz von ι ο bis 15 pCt. Leinölsäure oder Ricinusöl wird ein Lack erhalten, welcher heller ist als die bis jetzt bekannten fetten Lacke. Derselbe giebt, auf Naturholz gestrichen, ohne Anwendung von Porenfüllern oder dergleichen einen rasch trocknenden Ueberzug, welcher geschliffen und mit Leinöl polirt werden kann.1 part of crushed cowrie is poured over it with part dichlorohydrin or epichlorohydrin, the mixture is allowed to stand for some time, adds ι Add alcohol and heat until it is completely dissolved. After adding ι ο to 15 pct. Linseed oleic acid or castor oil gives a varnish which is lighter than the bis now known fat paints. The same gives, painted on natural wood, without application of pore fillers or the like a quick-drying coating, which is sanded and can be polished with linseed oil.

Claims (1)

Patent-Anspruch:Patent claim: Anwendung von Chlorhydrinen des Glycerins, insbesondere Dichlorhydrin und Epichlorhydrin, zum Auflösen von Bernstein und Copalen bei der Herstellung von Lacken.Use of glycerol chlorohydrins, especially dichlorohydrin and epichlorohydrin, for dissolving amber and copalene in the manufacture of lacquers. BERLIN. GEDRUCKT IN DER REICHSDRUCKEREI.BERLIN. PRINTED IN THE REICHSDRUCKEREI.
DENDAT84146D Active DE84146C (en)

Publications (1)

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Family

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Country Status (1)

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