US1041587A - Process of producing dyed cellulose ester. - Google Patents

Process of producing dyed cellulose ester. Download PDF

Info

Publication number
US1041587A
US1041587A US70298912A US1912702989A US1041587A US 1041587 A US1041587 A US 1041587A US 70298912 A US70298912 A US 70298912A US 1912702989 A US1912702989 A US 1912702989A US 1041587 A US1041587 A US 1041587A
Authority
US
United States
Prior art keywords
dyed
cellulose
cellulose ester
dyed cellulose
producing
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 - Lifetime
Application number
US70298912A
Inventor
Benno Borzykowski
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US70298912A priority Critical patent/US1041587A/en
Application granted granted Critical
Publication of US1041587A publication Critical patent/US1041587A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B3/00Preparation of cellulose esters of organic acids
    • C08B3/22Post-esterification treatments, including purification

Definitions

  • cellulose has first. been dyed and then etherized or prepared acetyl cellulose has been dyed by using swelling means or organic solvents whichareintended to produce receptivenes's of the cellulose esters which are otherwise indifferent to dyes.
  • the present process dyed cellulose esters which are exceedingly fast against light and washing are produced in a single process the dye being dissolved for example directly in the acidylizing mixture or in a portion of the acetic acid and thereafter the cellulose, hydroor oxy-cellulose (hereinafter-referred to as a cellulosic material) isbrought into this coloring solution by heating.
  • a cellulosic material hydroor oxy-cellulose
  • the dyed celluloseproducts pass clearly into the solution and can be further treated without alteration of the tint.
  • acetic acid which contains 2% of concentrated sulfuric acid
  • a solution of a dye such for example as Bismarck brown in 100 parts of acetic acid is added and the whole mass is heated in the water bath until a clear brown solution is produced.
  • a process of producing dyed cellulose esters comprising the simultaneous treatment of a cellulosic material with a suitable dye and an acidylizing agent.
  • a process of producing dyed cellulose acetate comprising the simultaneous treatment of a cellulosic material with a suitable dye and an acetylizing agent.
  • Aprocess of producing dyed cellulose esters comprising the simultaneous treatment of cellulose with a suitable dye and an acidylizing agent.
  • a process of producing dyed cellulose esters comprising the simultaneous treatment of a cellulosic material with a suitable dye and a mixture of acetic acid, acetic anhydrid and sulfuric acid.
  • a process of producing dyed cellulose esters-said process comprising the simulta- I neous treatment of a cellulosicmaterial with an acid-soluble dye and an acidylizing agent.

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)
  • Coloring (AREA)

Description

BEN-NO IBORZYKOWSKI, F CHARLOZITENBUBG, GERMANY.
rnocns s or rnonuctne DYED CELLULOSE ESTER.
1,041,587; No Drawing.
To all whom it m ay concern:
Be it known that I, BENNO BoRzYKow- SKI. a subject of the Emperor of Russia, and
resident of Charlottenburg, Germany, have invented a certain new and useful Improvement in Processes of Producing Dyed Cellulose Ester, of which the following is a specification.
Several processes are already known for dyeing acetyl cellulose or for producing it in a dyed condition. For example cellulose has first. been dyed and then etherized or prepared acetyl cellulose has been dyed by using swelling means or organic solvents whichareintended to produce receptivenes's of the cellulose esters which are otherwise indifferent to dyes.
In accordanceflwith .the present process dyed cellulose esters which are exceedingly fast against light and washing are produced in a single process the dye being dissolved for example directly in the acidylizing mixture or in a portion of the acetic acid and thereafter the cellulose, hydroor oxy-cellulose (hereinafter-referred to as a cellulosic material) isbrought into this coloring solution by heating. As there are now a large number of fastdyes which resist acids. by
the use of such suitable dyes. products brightly dyed and of exceedingly fast properties are produced by this very simple process without special precautionary measures.
introducing such 'a dyed-solution of formyla a'cetylor .propionyl-cellulose, etc., into one of the usual precipitating media such as water, benzol, alcohol and so on abrightand clearly dyed product in the desired form such as yarn, film, etc., which do not bleedin the precipitating bath, do not 7 give up the dye on further treatment, and
possess the same strength as in the uncolored condition. On treatment with the usual solvents such for example as chloroform,-
acetone, dichlor'ethylene, etc., the dyed celluloseproducts pass clearly into the solution and can be further treated without alteration of the tint.
I Example: 100 parts of cleaned and dried cotton is introduced and stirred into a mixture of 450 parts of acetic acid anhydrid and Specification of Letters Patent. Application filed l l'une 11, 1912. Serial No. 702,989.
Patented Oct. 15,1912.
400 parts of acetic acid which contains 2% of concentrated sulfuric acid; at the same time a solution of a dye such for example as Bismarck brown in 100 parts of acetic acid is added and the whole mass is heated in the water bath until a clear brown solution is produced.
Instead of dissolying the dye separately itcan be added directly to the acetylizing mixture and can be stirred in. The same results are obtained when the dye is added before heating or to the-prepared acetylizing mass.
The same process is carried out with other dyes. as, for example, metanile yellow, chrysophenin G, fastscarlet colors, substantive blacks, etc. l
The solutions of' dyed acidylized cellulose thus obtained can be further treated directly. T
1. A process of producing dyed cellulose esters, said process comprising the simultaneous treatment of a cellulosic material with a suitable dye and an acidylizing agent.
2. A process of producing dyed cellulose acetate, said process comprising the simultaneous treatment of a cellulosic material with a suitable dye and an acetylizing agent.
Aprocess of producing dyed cellulose esters. said process comprising the simultaneous treatment of cellulose with a suitable dye and an acidylizing agent.
4. A process of producing dyed cellulose esters, said process comprising the simultaneous treatment of a cellulosic material with a suitable dye and a mixture of acetic acid, acetic anhydrid and sulfuric acid.
5. A process of producing dyed cellulose esters-said process comprising the simulta- I neous treatment of a cellulosicmaterial with an acid-soluble dye and an acidylizing agent.
In testimony whereof I have signed my name to this specification in the prewng of two subscribing witnesses.
, BENNO BORZYKOWSKI.
\ Witnesses: v
' CLARENCE CoRRIoAN,
Martins Hammer.
US70298912A 1912-06-11 1912-06-11 Process of producing dyed cellulose ester. Expired - Lifetime US1041587A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US70298912A US1041587A (en) 1912-06-11 1912-06-11 Process of producing dyed cellulose ester.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US70298912A US1041587A (en) 1912-06-11 1912-06-11 Process of producing dyed cellulose ester.

Publications (1)

Publication Number Publication Date
US1041587A true US1041587A (en) 1912-10-15

Family

ID=3109862

Family Applications (1)

Application Number Title Priority Date Filing Date
US70298912A Expired - Lifetime US1041587A (en) 1912-06-11 1912-06-11 Process of producing dyed cellulose ester.

Country Status (1)

Country Link
US (1) US1041587A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2673202A (en) * 1951-11-14 1954-03-23 Eastman Kodak Co Method for the manufacture of high acetyl cellulose acetate

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2673202A (en) * 1951-11-14 1954-03-23 Eastman Kodak Co Method for the manufacture of high acetyl cellulose acetate

Similar Documents

Publication Publication Date Title
US2274751A (en) Materials
GB673738A (en) Improvements in or relating to methods of treating polymeric compositions and products thereof
US1041587A (en) Process of producing dyed cellulose ester.
US1812790A (en) Wolfgang jaeck
US2880106A (en) Manufacture of textile and other materials having a basis of cellulose triacetate
US1871470A (en) Dyeing of cellulose derivatives
GB353978A (en) Manufacture of cellulose esters
US2055686A (en) Method of removing impurities from dyestuffs
US1440501A (en) esajtce
US2102647A (en) Artificial effect material
US1927161A (en) Coloration of material
US701427A (en) Red dye and process of making same.
US994738A (en) Process of producing dyed-acidylized-cellulose compounds.
US2054913A (en) Manufacture of mixed fabkics com-
US1421290A (en) Method of preparing cellulose-ester products
US979966A (en) Process of dyeing acetyl-cellulose.
US806053A (en) Naphthalene dye and process of making same.
US2170190A (en) Organic materials
US1023890A (en) Process of treating brittle vegetable fibers of kapok and other plants.
GB226309A (en) Improvements in the manufacture of cellulose acetate
US1860473A (en) Compositions consisting of woolen fibers and artificial threads
US1789121A (en) Process for coloring cellulose esters and ethers
US1780836A (en) New vat dyestuffs
GB381943A (en) Improvements in processes for dyeing materials made from cellulose esters or ethers
GB301564A (en) Process for the dyeing of artificial silk comprising acyl derivatives or ethers of cellulose or of its conversion products