CH148481A - Process for the production of a new cellulose derivative. - Google Patents
Process for the production of a new cellulose derivative.Info
- Publication number
- CH148481A CH148481A CH148481DA CH148481A CH 148481 A CH148481 A CH 148481A CH 148481D A CH148481D A CH 148481DA CH 148481 A CH148481 A CH 148481A
- Authority
- CH
- Switzerland
- Prior art keywords
- cellulose derivative
- production
- epichlorohydrin
- new cellulose
- new
- 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
- C08B11/08—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals with hydroxylated hydrocarbon radicals; Esters, ethers, or acetals thereof
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 Zellalosedei:ivates. Es wurde gefunden, dass ein neuer Zellu- loseabkömmling entsteht, wenn man Zellulose mit Epichlorhydrin behandelt. Die Reaktion, die darin besteht, dass die Zellulose unter Aufspaltung des Oxydringes in einen Oxy- alkyläther verwandelt wird, wird zweckmässig durch die Gegenwart eines geeigneten Kata- lysators, wie zum Beispiel Schwefelsäure oder Borsäure beziehungsweise die entsprechenden Chlorhydrinester, beschleunigt.
Der neue Zelluloseabkömmling kann als Ausgangsstoff zur Herstellung von Textilien verwendet werden. Indessen wird der Schutz für das angegebene Verfahren nur soweit beansprucht, als es sich nicht um eine für die Textilindu strie in Betracht kommende Behandlung von Textilfasern zum Zwecke von deren Vered lung handelt.
Beispiel 20 gr gebleichte Linters werden mit einer 10 o/oigen wässerigen Borsäurelösung bei 60-70<B>0</B> imprägniert, gut abgepresst und dann getrocknet. Das so vorbehandelte Ma terial wird in einem geeigneten Apparat während 50 Stunden bei einer Temperatur von 120-130 o Epichlorhydrindämpfen ausgesetzt. <I>Beispiel 2:</I> 100 gr Epichlorhydrin werden unter guter Kühlung allmählich mit 3 gr konzentrierter Schwefelsäure versetzt.
Die so erhaltene Lösung des Chlorhydrinschwefelsäureesters in Epichlorhydrin wird in einem Druckgefäss mit 10 gr Linters während 35 Stunden auf 130-140 o erhitzt. Nach beendigter Reak tion werden die Linters abgepresst und sorg fältig ausgewaschen.
Der neue Zelluloseabkömmling ist rein weiss und enthält eine
EMI0001.0033
in welcher das Halogenatom beweglich ist.
Process for the production of a new cell alose dei: ivates. It has been found that a new derivative of cellulose arises when cellulose is treated with epichlorohydrin. The reaction, which consists in the cellulose being converted into an oxyalkyl ether with splitting of the oxide ring, is expediently accelerated by the presence of a suitable catalyst, such as sulfuric acid or boric acid or the corresponding chlorohydrin ester.
The new cellulose derivative can be used as a raw material for the manufacture of textiles. 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 their refinement that is suitable for the textile industry.
Example 20 g of bleached linters are impregnated with a 10% strength aqueous boric acid solution at 60-70%, pressed well and then dried. The material pretreated in this way is exposed to epichlorohydrin vapors in a suitable apparatus for 50 hours at a temperature of 120-130 o. <I> Example 2: </I> 100 grams of epichlorohydrin are gradually mixed with 3 grams of concentrated sulfuric acid while being well cooled.
The resulting solution of the chlorohydrin-sulfuric acid ester in epichlorohydrin is heated to 130-140 ° for 35 hours in a pressure vessel with 10 g linters. When the reaction is complete, the linters are pressed out and carefully washed out.
The new cellulose derivative is pure white and contains one
EMI0001.0033
in which the halogen atom is mobile.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH148481T | 1930-01-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH148481A true CH148481A (en) | 1931-07-31 |
Family
ID=4404294
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH148481D CH148481A (en) | 1930-01-11 | 1930-01-11 | Process for the production of a new cellulose derivative. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH148481A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE34904E (en) * | 1989-10-30 | 1995-04-11 | Hercules Incorporated | Alkylaryl hydrophobically modified cellulose ethers |
-
1930
- 1930-01-11 CH CH148481D patent/CH148481A/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE34904E (en) * | 1989-10-30 | 1995-04-11 | Hercules Incorporated | Alkylaryl hydrophobically modified cellulose ethers |
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