DE281262C - - Google Patents

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Publication number
DE281262C
DE281262C DENDAT281262D DE281262DA DE281262C DE 281262 C DE281262 C DE 281262C DE NDAT281262 D DENDAT281262 D DE NDAT281262D DE 281262D A DE281262D A DE 281262DA DE 281262 C DE281262 C DE 281262C
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DE
Germany
Prior art keywords
naphthalene
depending
added
intended
camphor
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.)
Expired
Application number
DENDAT281262D
Other languages
German (de)
Publication date
Application granted granted Critical
Publication of DE281262C publication Critical patent/DE281262C/de
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L5/00Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
    • C08L5/12Agar or agar-agar, i.e. mixture of agarose and agaropectin; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/01Hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/05Alcohols; Metal alcoholates
    • C08K5/053Polyhydroxylic alcohols
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L89/00Compositions of proteins; Compositions of derivatives thereof
    • C08L89/04Products derived from waste materials, e.g. horn, hoof or hair
    • C08L89/06Products derived from waste materials, e.g. horn, hoof or hair derived from leather or skin, e.g. gelatin
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L93/00Compositions of natural resins; Compositions of derivatives thereof

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Dermatology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

KAISERLICHESIMPERIAL

PATENTAMT.PATENT OFFICE.

PATENTSCHRIFTPATENT LETTERING

KLASSE 39 b. GRUPPECLASS 39 b. GROUP

JULIUS STOCKHAUSEN in CREFELD.JULIUS STOCKHAUSEN in CREFELD.

Zusatz zum Patent 277653. Addendum to patent 277653.

Patentiert im Deutschen Reiche vom 23. Dezember 1910 ab. Längste Dauer: 16. April 1925.Patented in the German Empire on December 23, 1910. Longest duration: April 16, 1925.

Das im Patent 277653 beschriebene Verfahren läßt sich auch in der Weise ausführen, daß der Kampfer ersetzt wird durch Naphtalin oder sonstige zyklische Kohlenwasserstoffe (z. B. Kumol, Mesitylen und höhere Homologe), soweit dieselben als Kampferersatzmittel in der Zelluloidindustrie in Betracht kommen. Es ist bereits bekannt, Kasein und vegetabilischen Eiweißstoffen Naphtol zuzusetzen und so einen Zelluloidersatz herzustellen. Die mit Naphtalin hergestellte Masse weist jedoch eine erheblich größere Zug- und Druckelastizität auf, als die mit Naphtol hergestellte. The method described in patent 277653 can also be carried out in such a way that the camphor is replaced by naphthalene or other cyclic hydrocarbons (e.g. cumene, mesitylene and higher homologues), insofar as they are used as camphor substitutes in the celluloid industry. It is already known to casein and add naphtol to vegetable proteins and thus produce a celluloid substitute. The mass produced with naphthalene, however, has a considerably greater tensile and tensile strength Compressive elasticity than that made with naphthol.

Im folgenden ist ein Aüsführungsbeispiel zur praktischen Durchführung des Verfahrens angeführt. Die angegebenen Zahlen sollen keine Grenzwerte bedeuten, vielmehr können die Ansätze je nach der beabsichtigten Qualität der herzustellenden Waren auch noch entsprechend abgeändert werden. Auch ist es keineswegs nötig, stets die genannten Härtungsmittel anzuwenden, es können auch andere Härtungsmittel und Gemische von solchen benutzt werden. Auch die Menge des zuzusetzenden Härtungsmittels kann je nach Auswahl der sonstigen Zusätze und je nach der beabsichtigten Konsistenz des herzustellenden Produkts verringert oder auch noch wesentlich vermehrt werden. ■The following is an exemplary embodiment for practicing the method cited. The numbers given are not intended to mean limit values, but rather can the approaches depending on the intended quality of the goods to be manufactured also accordingly be modified. It is also by no means necessary to always use the hardening agents mentioned other hardeners and mixtures of these can also be used. Also the amount of to be added hardening agent can depending on the selection of other additives and depending on the intended consistency of the product to be manufactured or even reduced be increased significantly. ■

125 g Gelatine oder Agar-Agar, gepulvert·, werden in 125 g Glyzerin, 280 Be, roh, bei einer 750 nicht übersteigenden Temperatur gelöst, dann mit 15 g Holzteer usw. versetzt. Darauf wird 25 g Naphtalin oder besser eine dieser Naphtaiinmenge entsprechende Naphta- . linlösung von zweckmäßig 250 und endlich 20 g Formaldehyd in vierprozentiger Lösung zugefügt. Die erhaltene Mischung kann in beliebige Formen gegossen werden.125 g gelatine or agar-agar, powdered, are dissolved in 125 g glycerine, 28 0 Be, raw, at a temperature not exceeding 75 0 , then mixed with 15 g wood tar etc. Then 25 g of naphthalene or, better, a naphthalene corresponding to this amount of naphthalene is added. lin solution of expediently 25 0 and finally 20 g of formaldehyde in four percent solution added. The mixture obtained can be poured into any shape.

Claims (1)

Patent-An Spruch:Patent-An saying: Eine weitere Ausbildung des Verfahrens nach Patent 277653, darin bestehend, daß der dort als Zusatz zu den Kolloidstoffen verwendete Kampfer hier durch Naphtalin oder andere zyklische Kohlenwasserstoffe ersetzt wird.Another embodiment of the method according to patent 277653, consisting in that the camphor used there as an additive to the colloidal substances here through naphthalene or other cyclic hydrocarbons is replaced.
DENDAT281262D Expired DE281262C (en)

Publications (1)

Publication Number Publication Date
DE281262C true DE281262C (en) 1900-01-01

Family

ID=537019

Family Applications (1)

Application Number Title Priority Date Filing Date
DENDAT281262D Expired DE281262C (en)

Country Status (1)

Country Link
DE (1) DE281262C (en)

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