CH142749A - Process for the production of a new cellulose derivative. - Google Patents
Process for the production of a new cellulose derivative.Info
- Publication number
- CH142749A CH142749A CH142749DA CH142749A CH 142749 A CH142749 A CH 142749A CH 142749D A CH142749D A CH 142749DA CH 142749 A CH142749 A CH 142749A
- Authority
- CH
- Switzerland
- Prior art keywords
- cellulose derivative
- cellulose
- new
- production
- dyes
- 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
- C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
- C08B15/05—Derivatives containing elements other than carbon, hydrogen, oxygen, halogens or sulfur
- C08B15/06—Derivatives containing elements other than carbon, hydrogen, oxygen, halogens or sulfur containing nitrogen, e.g. carbamates
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)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Description
Verfahren zur Herstellung eines neuen Zellulosederivates. Es wurde befunden, dass man ein neues Zellulosederivat erhält, wenn man auf Zellu lose unter Beibehaltung der äussern Struktur Phenylisocyanat einwirken lässt.
Die Zellulose ist äusserlich unverändert. hat an Gewicht zugenommen und ist stick stoffhaltig. Das neue Zellulosedc rivat wird von basischen Farbstoffen ohne Beizmittel kräftig angefärbt. hat auch zu Acetatseide farbstoffen Verwandtschaft, währenddem Direktfarbstoffe kaum aufgenommen werden. Das neue Produkt kann als Rohstoff zur Herstellung von Textilfasern verwendet werden. Indesson wird der Schutz für das angegebene Verfahren nur soweit bean sprucht als es sich nicht um eine für die Textilindustrie in Betracht kommende Be handlung von Textilfasern zum Zwecke de ren Veredlung handelt.
Beispiel 1: Man legt im Vakuum getrocknete Zellu lose (Zellstoff. Baumwolle, Linters. Viskose) in Phenvlisocyanat ein und erwärmt unter Zuhabe einer beringen Menge troelieinen Py- en ridins s auf 80 . Nach vier Stundun wird da- überschüssige Isocyanat im Vakuum all destilliert und das neue Zellulosederivat durch Waschen mit heissem Alkohol von den verbleibenden Resten Pyridin und von etwa gebildetem Diphenylharmstoff befreit. Beispiel 2: Man legt Zellulose in eine Mischung von 90 Teilen Phenylisocyanat und I0 Teilen Pyridin ein. Maii buh ässt vier Tage iii der Mischung und entfernt den Übcrschuss voll Phenylisocyant und Pyridin durch Ab destillieren im Vakuum oder durch Ab schleudern.
Man wäscht schliesslich mit heissem Alkohol.
Ein Produkt mit gleichen Eigenschaften wird erhalten. wenn die ssehandlung der Zellulose mit Phenvlisocyant in Abwesen heit von Pyridin, in Gegenwart von Kataly - satoren. wie Chlorzink. oder von Verdün- nungsnmitteln durchgeführt wird.
Process for the production of a new cellulose derivative. It was found that a new cellulose derivative is obtained if phenyl isocyanate is allowed to act on cellulose while retaining the external structure.
The cellulose is externally unchanged. has gained weight and contains nitrogen. The new cellulose derivative is strongly colored by basic dyes without a mordant. is also related to acetate silk dyes, whereas direct dyes are hardly absorbed. The new product can be used as a raw material for the manufacture of textile fibers. However, protection for the specified process is only claimed insofar as it does not involve a treatment of textile fibers for the purpose of their refinement that is suitable for the textile industry.
Example 1: Cellulose (cellulose, cotton, linters, viscose) which has been dried in a vacuum is placed in phenyl isocyanate and heated to 80 with the addition of a ring-shaped amount of troeline pyridine. After four hours, the excess isocyanate is all distilled off in vacuo and the new cellulose derivative is freed from the remaining pyridine and any diphenylharm that has formed by washing with hot alcohol. Example 2: Cellulose is placed in a mixture of 90 parts of phenyl isocyanate and 10 parts of pyridine. Maii buh soaks the mixture for four days and removes the excess phenyl isocyanate and pyridine by distilling off in vacuo or by centrifuging.
Finally, wash with hot alcohol.
A product with the same properties is obtained. if the cellulose is treated with phenolic isocyanate in the absence of pyridine, in the presence of catalysts. like zinc chloride. or by diluents.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH142749T | 1928-08-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH142749A true CH142749A (en) | 1930-10-15 |
Family
ID=4399466
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH142749D CH142749A (en) | 1928-08-08 | 1928-08-08 | Process for the production of a new cellulose derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH142749A (en) |
-
1928
- 1928-08-08 CH CH142749D patent/CH142749A/en unknown
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