US2097120A - Manufacture of nitrogenous cellulose derivatives - Google Patents

Manufacture of nitrogenous cellulose derivatives Download PDF

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Publication number
US2097120A
US2097120A US35402A US3540235A US2097120A US 2097120 A US2097120 A US 2097120A US 35402 A US35402 A US 35402A US 3540235 A US3540235 A US 3540235A US 2097120 A US2097120 A US 2097120A
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Prior art keywords
imine
ethylene
nitrogen
cellulose
cellulose derivatives
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US35402A
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Fink Heinrich
Bitterfeld Wolfen Kries
Stahn Richard
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IG Farbenindustrie AG
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IG Farbenindustrie AG
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P5/00Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
    • D06P5/22Effecting variation of dye affinity on textile material by chemical means that react with the fibre
    • D06P5/225Aminalization of cellulose; introducing aminogroups into cellulose

Definitions

  • One of its objects is to provide a process of manufacturing nitrogenous cellulose derivatives.
  • imine may be brought to reaction'on cellulose at a raised temperature in gaseous form; this may be easily realized in view of the low boiling point of 4 the ethylene-imine.
  • the ethyleneimine may also be brought intci reaction with the I cellulosic material while dissolved in a suitable solvent which does not react with the-ethyleneimine.
  • suitable solvents are, for instance, water, or organic solvents, for instance, toluene, xylene, benzene or highly boiling benzene, that is to say aromatic and aliphatic hydrocarbons.
  • the process according to this invention is of particular importance for the treatment of cellulosic fibers which are intended to be dyed by acid wool dyes, because the treated fibers must not be pretreated with a lye or the like before dyeing. If the treatment of the cellulosic material is not performed in an aqueous solution the cellulosic material is preferably used in air dry condition.
  • the cellulosic material may also be used while having a lesser content of moisture, however, in this case the speed of the reaction is decreased.
  • the interaction occurs at temperatures from room temperature up to 120 C., the range from 80 to 100 C. being preferred.
  • the fibers are washed with an acid solution and then with water. At a higher .temperature a greater amount of nitrogen is introduced into the cellulosic material, 0 and the remaining conditions being the same a higher content of nitrogen is taken up by the fibers if the cellulosic material contains more moisture.
  • the treatment with imine is repeated several times, whereupon the fibers are thoroughly washed with hot water. In this manner there may be reached a content of n1.- trogen of 10% and more.
  • Example 1 Example 1.-55 grams of air-dry viscose staple fiber whichhave been subjected to avacuum in an autoclave are heated at 100 C in the latter 5 with 10 cc. of ethylene-imine vapour for 4' hours. After this time has elapsed the ethylene-imine has completely disappeared. The fiber is washed with water, with'dilute sulfuric acid and again with'water. It is feebly yellow, contains 2.45 10 percent. of nitrogen and is dyed very strongly by acid wool-dyestuffs.
  • Example 2 55 grams of dry viscose staple amiple 1, "with 10 cc. or ethylene-imine for 5 /21 hours.
  • the product, treated as described in Example 1, contains 1.63 percent. of nitrogen.
  • Example 5250 gramsof artificial silk cut into staples are introduced into a solution of 50 cc. of ethylene-imine in 5 liters of toluene and heated to C. while repeatedly shaking. Hereafter the toluene is removed by suction and the fibers washed with methanol and water and dried. The fibers contain 2.07% ofnitrogen.
  • Example 6 In a cylindrical vessel of 10liters capacity there are introduced 5 kilos of artificial silk from viscose tightly packed between two sieves. The lids of the 'vessel infront of the sieves are provided with an inlet and an out- 40 let tube. After thefibers have been introduced the vessel is closed and the inlet and outlet. tube are'connected with a pump for the production of a gas circulation of about liters per minute. The whole apparatus is then heated to 45 80 C., and then there are introduced into the gas circulation 1200 cc. of ethylene-imine in the 1 course of half an hour. The ethylene-imine befrom linters are pressed into a solution of cc. of ethylene-irnine dissolved in cc.
  • the fibers have the following content of nitrogen after the single operations:
  • a process of producing cellulose derivatives containing nitrogen which comprises introducing artificial silkfrom viscose cut in staples tightly packed into a vessel, heating said vessel to 80C. and circulating a current of gaseous ethyleneimine at a temperature ofa0 C. through said fibers.
  • a process of producing cellulose derivatives containing nitrogen which comprises introducing artificialsilk from viscose cut in staples tightly packed into a vessel, heating said vessel to 80 C. andcirculating a current of gaseous ethyleneimine at a temperature of 80 0. through said fibers while changing the direct-ion of the current of gasperiodically.
  • a process of producing cellulose derivatives containing nitrogen which comprises heating artificial silk made fromlinters with a solution of 20 cc. of ethylene-imine in 80cc. of water in a sealed vessel,,t o 100 C., washing the resulting product, and-repeating this operation Several times.
  • a process of producing celllllose derivatives containing nitrogen which comprises heating artificial .silk from viscose cut in staples with ethylene- -irnine to 100 C. in apressure vessel,

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Artificial Filaments (AREA)

Description

Patented Oct. 26, 1937 MANUFACTURE OF NITROGENOUS CELLU- LOSE DERIVATIVES- Heinrich Fink. Wolfen Kries Bitterfeld, and Richard Stahn, Dessau. Germany, assignors to I. G. Farbenindustrie Aktiengcsellschaft,
Frankfort-on-the-Main, Germany No Drawing.
Application August 8, 1935, Serial No. 35,402. In Germany August .14, 1934 8 Claims. I (01. 260-152) Our present inventionrelates to the manufacture of cellulose. e I
One of its objects is to provide a process of manufacturing nitrogenous cellulose derivatives.
imine may be brought to reaction'on cellulose at a raised temperature in gaseous form; this may be easily realized in view of the low boiling point of 4 the ethylene-imine. The ethyleneimine may also be brought intci reaction with the I cellulosic material while dissolved in a suitable solvent which does not react with the-ethyleneimine. Such solvents are, for instance, water, or organic solvents, for instance, toluene, xylene, benzene or highly boiling benzene, that is to say aromatic and aliphatic hydrocarbons. The process according to this invention is of particular importance for the treatment of cellulosic fibers which are intended to be dyed by acid wool dyes, because the treated fibers must not be pretreated with a lye or the like before dyeing. If the treatment of the cellulosic material is not performed in an aqueous solution the cellulosic material is preferably used in air dry condition.
The cellulosic material may also be used while having a lesser content of moisture, however, in this case the speed of the reaction is decreased. The interaction occurs at temperatures from room temperature up to 120 C., the range from 80 to 100 C. being preferred. After the treatment with ethylene-imine the fibers are washed with an acid solution and then with water. At a higher .temperature a greater amount of nitrogen is introduced into the cellulosic material, 0 and the remaining conditions being the same a higher content of nitrogen is taken up by the fibers if the cellulosic material contains more moisture. V
When treating the cellulosic material with gaseous ethylene-imine there is obtained a more uniform product when circulating the current of gas and changing periodically the direction of the current.
If thecellulosic material is to receive a higher content of nitrogen the treatment with imine is repeated several times, whereupon the fibers are thoroughly washed with hot water. In this manner there may be reached a content of n1.- trogen of 10% and more.
' fiber are heated at 100 C; as d'escribedin Ex:-
ethylene-imine in 90 cc. of water and heated The following examples illustrate the invention: I Example 1.-55 grams of air-dry viscose staple fiber whichhave been subjected to avacuum in an autoclave are heated at 100 C in the latter 5 with 10 cc. of ethylene-imine vapour for 4' hours. After this time has elapsed the ethylene-imine has completely disappeared. The fiber is washed with water, with'dilute sulfuric acid and again with'water. It is feebly yellow, contains 2.45 10 percent. of nitrogen and is dyed very strongly by acid wool-dyestuffs.
Example 2.55 grams of dry viscose staple amiple 1, "with 10 cc. or ethylene-imine for 5 /21 hours. The product, treated as described in Example 1, contains 1.63 percent. of nitrogen.
Example 3.55 grams of air-dry viscose staple fiber (8 per cent H2O) are in a vacuum treated for 23 hours as described in the preceding examples, with 10 cc of ethylene-imine, at C. The product contains 1.73 per cent of nitrogen. Example 4.100 grams of artificial silk cut into. staples are pressed into a solution of 10 cc. of 25 while sealed for about 2 hours to 100 C. The washed product contains 1.44% of nitrogen.
Example 5.250 gramsof artificial silk cut into staples are introduced into a solution of 50 cc. of ethylene-imine in 5 liters of toluene and heated to C. while repeatedly shaking. Hereafter the toluene is removed by suction and the fibers washed with methanol and water and dried. The fibers contain 2.07% ofnitrogen.
. Example 6.-In a cylindrical vessel of 10liters capacity there are introduced 5 kilos of artificial silk from viscose tightly packed between two sieves. The lids of the 'vessel infront of the sieves are provided with an inlet and an out- 40 let tube. After thefibers have been introduced the vessel is closed and the inlet and outlet. tube are'connected with a pump for the production of a gas circulation of about liters per minute. The whole apparatus is then heated to 45 80 C., and then there are introduced into the gas circulation 1200 cc. of ethylene-imine in the 1 course of half an hour. The ethylene-imine befrom linters are pressed into a solution of cc. of ethylene-irnine dissolved in cc. of water in a pressure vessel and heated to C. for 2 hours. The fibers are washed and a-new treated with imine in the same manner. This operation is performed 7 times with thedifi'erence that the last two times there are applied only 10 cc. of imine. The fibers have the following content of nitrogen after the single operations:
Percent N 1. Treatment 0.84 2. Treatment 1.97 3. Treatment 3.57 4. Treatment 5.34 5. Treatment 8.11. 6. Treatment 8.83; 7. Treatment 9.48
When heating a cellulosic material treated according to this invention and containingat least 1% of nitrogen with a 2 per cent solution of furfurol'to 100 -C. the material assumes a dark brown color. Nitrogen containing cellulosic materials made according to other processes re! mai'n-uncolored or assume only a yellow color when treated in the manner.
Whatwe claim is: v
1. A process of introducing nitrogen into cellulose" according to which cellulose is subjected to the action of ethylene-imine. 4
2. A process of introducing nitrogen into cellulose according to which cellulose is subjected to the action of ethylene-iminejn gaseous con dition. V
3. A process of introducing nitrogen into cellulose according to which cellulose isfsubjected to the action of ethylene-imine dissolved in a solvent which does not react with ethylene-imine.
4. A process of introducing nitrogen into cellulose according to which cellulose is subjected to the action of ethylene-imine at a temperature between 80 to 100 C.
5. A process of producing cellulose derivatives containing nitrogen which comprises introducing artificial silkfrom viscose cut in staples tightly packed into a vessel, heating said vessel to 80C. and circulating a current of gaseous ethyleneimine at a temperature ofa0 C. through said fibers.
6. A process of producing cellulose derivatives containing nitrogen which comprises introducing artificialsilk from viscose cut in staples tightly packed into a vessel, heating said vessel to 80 C. andcirculating a current of gaseous ethyleneimine at a temperature of 80 0. through said fibers while changing the direct-ion of the current of gasperiodically.
7. A process of producing cellulose derivatives containing nitrogen which comprises heating artificial silk made fromlinters with a solution of 20 cc. of ethylene-imine in 80cc. of water in a sealed vessel,,t o 100 C., washing the resulting product, and-repeating this operation Several times.
. 8. A process of producing celllllose derivatives containing nitrogen which comprises heating artificial .silk from viscose cut in staples with ethylene- -irnine to 100 C. in apressure vessel,
with dilute sulfuric acid, and again with water. HEINRICH FINK.
I RICHARD STAHN.
-washing. the resultingproduct with water, then
US35402A 1934-08-14 1935-08-08 Manufacture of nitrogenous cellulose derivatives Expired - Lifetime US2097120A (en)

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2518676A (en) * 1946-05-15 1950-08-15 Eastman Kodak Co Animalizing of cellulose acetate
US2538903A (en) * 1947-05-09 1951-01-23 Keever Starch Company Uniformly substituted esters of glucopyranose polymers
US2621174A (en) * 1947-05-09 1952-12-09 Keever Starch Company Amino derivatives of glucopyranose polymers
US2656241A (en) * 1951-05-11 1953-10-20 Jr George L Drake Further aminized aminoalkylated celluloses by reacting with ethylenimine
US2972606A (en) * 1956-05-31 1961-02-21 Wyandotte Chemicals Corp Catalytic aminoethylation of cellulose, cellulose derivatives or polyvinyl alcohol
US4343646A (en) * 1979-12-10 1982-08-10 Calspan Corporation Method for producing fertilizer from waste paper

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2518676A (en) * 1946-05-15 1950-08-15 Eastman Kodak Co Animalizing of cellulose acetate
US2538903A (en) * 1947-05-09 1951-01-23 Keever Starch Company Uniformly substituted esters of glucopyranose polymers
US2621174A (en) * 1947-05-09 1952-12-09 Keever Starch Company Amino derivatives of glucopyranose polymers
US2656241A (en) * 1951-05-11 1953-10-20 Jr George L Drake Further aminized aminoalkylated celluloses by reacting with ethylenimine
US2972606A (en) * 1956-05-31 1961-02-21 Wyandotte Chemicals Corp Catalytic aminoethylation of cellulose, cellulose derivatives or polyvinyl alcohol
US4343646A (en) * 1979-12-10 1982-08-10 Calspan Corporation Method for producing fertilizer from waste paper

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