CH141556A - Process for the production of a new cellulose derivative. - Google Patents
Process for the production of a new cellulose derivative.Info
- Publication number
- CH141556A CH141556A CH141556DA CH141556A CH 141556 A CH141556 A CH 141556A CH 141556D A CH141556D A CH 141556DA CH 141556 A CH141556 A CH 141556A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- cellulose derivative
- cellulose
- new
- new cellulose
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B11/00—Preparation of cellulose ethers
- C08B11/02—Alkyl or cycloalkyl ethers
- C08B11/04—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals
- C08B11/14—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals with nitrogen-containing groups
- C08B11/145—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals with nitrogen-containing groups with basic nitrogen, e.g. aminoalkyl ethers
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Description
Verfahren zur Herstellung eines neuen Zellnlosederivates. Es wurde gefunden, dass man ein neues Zellulosederivat erhält, wenn man auf Al kalizellulose eine Verbindung der Formel-
EMI0001.0003
einwirken lässt.
Das neue Zellulosederivat ist durch seine basischen Eigenschaften ausgezeichnet und hat Affinität zu den meisten sauren Farb stoffen. Es ist in den üblichen Lösungs mitteln für Zellulose löslich und lässt sich daraus in beliebiger Form wiedergewinnen. Das Produkt kann als Rohstoff zur Her stellung von Textilfasern verwendet werden. Indessen wird der Schutz für das angege bene Verfahren nur soweit beansprucht, als es sich nicht um eine für die Textilindu strie in Betracht kommende Behandlung von Textilfasern zum Zwecke von deren Ver edlung handelt.
Beispiel <I>1:</I> 16 Teile Zellulose (Zellstoff, Baumwolle, Linters, regenerierte Zellulose etc.) werden in 160 Teile 18%ige Natronlauge eingelegt. Nach 3 Stunden zentrifugiert man die über schüssige Lauge ab und ,geht mit der Zel lulose in eine Lösung von 7 Teilen Chlor- äthyldiäthylamin in Aceton. Man lässt unter häufigem Durchrühren 3 Stunden in der Lö sung und wäscht hernach mit Wasser und schliesslich mit verdünnter Essigsäure, wo rauf man die Zellulose trocknet.
Man erhält eine hellgefärbte Masse, die mit sauren Farb stoffen färbbar ist.
Das Verfahren lässt sich auch auf gelöste Alkalizellulose anwenden. Dran kann auch das neue Erzeugnis in weitere Zellulose derivate umwandeln - zum Beispiel durch Xanthogenieren, Acetylieren usw. - und hierauf weiter verarbeiten.
<I>Beispiel 2</I> Man führt 15 Teile lose Baumwolle in N atronzellulose über und fügt nach dem Ab pressen 18 Teile Chloräthyldiäthylaminchlor- hydrat zu. Durch das überschüssige Alkali wird die organische Base in Freiheit gesetzt. Man knetet 8 Stunden lang durch, worauf man auswäscht. Das erhaltene neue Zellu- losederivat kann als solches verwendet wer den, oder zur Herstellung weiterer Zellulose derivate.
Process for the production of a new cellless derivative. It has been found that a new cellulose derivative is obtained if a compound of the formula
EMI0001.0003
can act.
The new cellulose derivative is characterized by its basic properties and has an affinity for most acidic dyes. It is soluble in the usual solvents for cellulose and can be recovered from it in any form. The product can be used as a raw material for the manufacture of textile fibers. In the meantime, protection for the specified process is only claimed insofar as it does not involve a treatment of textile fibers for the purpose of refining them that is suitable for the textile industry.
Example <I> 1 </I> 16 parts of cellulose (cellulose, cotton, linters, regenerated cellulose, etc.) are placed in 160 parts of 18% sodium hydroxide solution. After 3 hours, the excess liquor is centrifuged off and the cellulose is dissolved in a solution of 7 parts of chloroethyl diethylamine in acetone. It is left in the solution for 3 hours with frequent stirring and then washed with water and finally with dilute acetic acid, whereupon the cellulose is dried.
A light-colored mass is obtained which can be colored with acidic dyes.
The process can also be applied to dissolved alkali cellulose. On it, the new product can also be converted into further cellulose derivatives - for example by xanthating, acetylating, etc. - and then processed further.
<I> Example 2 </I> 15 parts of loose cotton are transferred into nitrocellulose and, after pressing, 18 parts of chloroethyl diethylamine chlorohydrate are added. The organic base is set free by the excess alkali. You knead for 8 hours, after which you wash out. The new cellulose derivative obtained can be used as such or for the production of further cellulose derivatives.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH141556T | 1928-08-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH141556A true CH141556A (en) | 1930-08-15 |
Family
ID=4398437
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH141556D CH141556A (en) | 1928-08-31 | 1928-08-31 | Process for the production of a new cellulose derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH141556A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2459222A (en) * | 1947-06-13 | 1949-01-18 | John D Guthrie | Introduction of amino groups into cellulose |
DE4417211A1 (en) * | 1994-05-17 | 1995-11-23 | Hoechst Ag | Modified cellulose@ synthetic fibres with affinity for reactive dyes |
US5565007A (en) * | 1994-05-17 | 1996-10-15 | Hoechst Aktiengesellschaft | Amination of rayon |
-
1928
- 1928-08-31 CH CH141556D patent/CH141556A/en unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2459222A (en) * | 1947-06-13 | 1949-01-18 | John D Guthrie | Introduction of amino groups into cellulose |
DE4417211A1 (en) * | 1994-05-17 | 1995-11-23 | Hoechst Ag | Modified cellulose@ synthetic fibres with affinity for reactive dyes |
US5565007A (en) * | 1994-05-17 | 1996-10-15 | Hoechst Aktiengesellschaft | Amination of rayon |
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