US2416890A - Manufacture of fibers and foils - Google Patents

Manufacture of fibers and foils Download PDF

Info

Publication number
US2416890A
US2416890A US328374A US32837440A US2416890A US 2416890 A US2416890 A US 2416890A US 328374 A US328374 A US 328374A US 32837440 A US32837440 A US 32837440A US 2416890 A US2416890 A US 2416890A
Authority
US
United States
Prior art keywords
solution
viscose
foils
fibers
filaments
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
US328374A
Other languages
English (en)
Inventor
Amende Joachim
Ender Willbald
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
Application granted granted Critical
Publication of US2416890A publication Critical patent/US2416890A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/52General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
    • D06P1/5264Macromolecular compounds obtained otherwise than by reactions involving only unsaturated carbon-to-carbon bonds
    • D06P1/5278Polyamides; Polyimides; Polylactames; Polyalkyleneimines
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L1/00Compositions of cellulose, modified cellulose or cellulose derivatives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L1/00Compositions of cellulose, modified cellulose or cellulose derivatives
    • C08L1/08Cellulose derivatives
    • C08L1/22Cellulose xanthate
    • C08L1/24Viscose
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F2/00Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
    • D01F2/06Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from viscose
    • D01F2/08Composition of the spinning solution or the bath
    • D01F2/10Addition to the spinning solution or spinning bath of substances which exert their effect equally well in either
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/58Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
    • D01F6/60Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides

Definitions

  • This invention relates to the manufacture of fibers and foils.
  • a further object is to produce these fibers and foils from viscose solutions treated with superpolyamides.
  • a still further object is the provision of fibers and foils from ammoniacal copper oxyde solutions treated with superpolyamides.
  • the superpolyamides obtained are practically colorless, resin-free substances which can be HOOC.
  • the superpolyamides obtained are soluble. in aqueous alkalies in contrast to the obtained are better than those of fibers and known superpolyamides which do not contain their color.
  • the fabrics or fib 2- sulfamide groups Due to this property they are suited especially for the refining of textile fibers, particularly as sizing agents.
  • solutions of viscose or of cellulose in ammoniacal copper oxyde are preferably mixed with alkaline solutions of these superpolyamides and then spun in a known man: ner or worked up into foils.
  • the usual coagulation agents like salt solutions or acids may be employed.
  • the quantity of the superpolyamides, to be given to the spinning solution may vary within wide limits. Preferably there are added not less than 5 per cent superpolyas otherwise the admixture of superpolyamides is of no practical value. On the other hand a multiple of superpolyamide compared with cellulose may be employed.
  • the fibers obtained are faster to possess a far higher Bauschelastizitat" (bolsterelasticity) and a more elastic grip than viscosefibers.
  • the grip moreover, on account of the good Bauschelastizitat resembles wool.
  • the dyeing properties of the fibers and foils thus foils from .pure viscose or pure ammoniacal copper oxyde cellulose. They absorb dyestuffs for instance much easier and Carl be dyed in darker shades than pure viscose or pure ammoniacal copper oxyde cellulose. Contrary to these they may be dyed with acid dyestuffs, for instance with wool dyestuffs and also with acetate silk dyestufl's. On account of the excellent dyeing properties the fibers are very much adapted for the manufacture of mixed fabrics.
  • Example I parts by weight of N.N-di-propanecarboxacid-p-sulfo-benzoic-acid-amide Wrinkling and lowish color and is over, possess contrary to page 131) by adding product consisting of soluble in a concentrated aqueous alkali solution. It can be drawn into filaments in the molten state.
  • Example III An alkaline solution of a s'uperpolyamideconsisting of 1 mol N.N-dipropanecarboxylic-acidp-sulfobenzoic-acid-diamide, 1 mol adipic acid and 2 mols hexamethylenediamine is added to a viscose solution capable of being spun in such a quantity, that the finished filaments contain about 20 per cent superpolyamide.
  • the filaments are dyed by boiling one hour with 2 per cent Sirius Fast Blue (Schultz dyestufi tables, year 1934, supplementary volume I, page 131) ratio of the weights of filaments and water Glauber salt. Far darker shades than on filaments consisting of superpolyamide-free viscose are thus obtained.
  • a process for the foils from a mixture of an superpolyamide containing sulfamide groups and a cellulosic solution selected from the group'con- 'sisting of viscose and ammoniacal copper oxide cellulose which comprises adding to the cellulosic solution an alkaline solution of thesuperpolyamide, the amount of superpolyamide added to the cellulosic solution being at least 5%, based on no0o.cHi.0H,.onmnsofiogsomn.among.ontooon and 6 parts by weight of hexamethylenediamine I are condensed as described in Example I.
  • the process for the foils from a mixture of an superpolyamide containing sulfamide groups and a cellulosic solution selected from the group'con- 'sisting of viscose and ammoniacal copper oxide cellulose which comprises adding to the cellulosic solution an alkaline solution of thesuperpolyamide, the amount of superpolyamide added to
  • a new filament as in claim 11 in which the based on the weight, of the cellulose, of an alkali-soluble linear superviscose solution.
  • a new filament comprising regenerated viscose cellulose containing at least five percent, based on the cellulose, and dissolved in the viscose solution from which the filament is formed, of an alkali-soluble linear superpolyamide containing sulfamide groups, said filament being resistan't to wrinkling, wool-like in character and readily dyed by acid and acetate silk dyes.
  • Filaments and foils comprising essentially a mixture of regenerated cellulose derived from a cellulosic solution selected from the group consisting of viscose and ammoniacal copper oxide cellulose. and at least five percent, based on the weight of the cellulose, of an alkali-soluble linear superpolyamide containing sulfamide groups. the superpolyamide being dissolved in the cellulosic solution, said filaments and foils being resistant to wrinkling, readily dyed by acid and acetate silk dyes and having been obtained by the process of claim 1.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Artificial Filaments (AREA)
US328374A 1939-03-29 1940-04-06 Manufacture of fibers and foils Expired - Lifetime US2416890A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE218047X 1939-03-29

Publications (1)

Publication Number Publication Date
US2416890A true US2416890A (en) 1947-03-04

Family

ID=5831074

Family Applications (1)

Application Number Title Priority Date Filing Date
US328374A Expired - Lifetime US2416890A (en) 1939-03-29 1940-04-06 Manufacture of fibers and foils

Country Status (5)

Country Link
US (1) US2416890A (enrdf_load_stackoverflow)
BE (1) BE438483A (enrdf_load_stackoverflow)
CH (1) CH218047A (enrdf_load_stackoverflow)
FR (1) FR873775A (enrdf_load_stackoverflow)
NL (1) NL54509C (enrdf_load_stackoverflow)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2571995A (en) * 1948-02-24 1951-10-23 Gen Mills Inc N, n'-diacyl aryl disulfonamides
US2901813A (en) * 1953-10-20 1959-09-01 American Viscose Corp Textile material of regenerated cellulose containing a polyacrylamide

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1203419B (de) * 1957-05-09 1965-10-21 Schwarza Chemiefaser Verfahren zum Herstellen von mattierten Fasern oder Faeden aus Hydratcellulose
FR2478116B1 (fr) * 1980-03-14 1985-06-14 Rhone Poulenc Textile Solutions conformables a partir de melanges de cellulose et polyamide-imide et articles en forme obtenus

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US950435A (en) * 1908-12-22 1910-02-22 Henri Louis Joseph Chavassieu Process of obtaining proteo-cellulosic products.
US1864426A (en) * 1929-10-25 1932-06-21 Henry A Gardner Delustered regenerated cellulose
US2071251A (en) * 1931-07-03 1937-02-16 Du Pont Fiber and method of producing it
US2130948A (en) * 1937-04-09 1938-09-20 Du Pont Synthetic fiber
US2136928A (en) * 1934-12-10 1938-11-15 Ig Farbenindustrie Ag Manufacture of amines of high molecular weight, which are rich in nitrogen
US2149273A (en) * 1937-01-13 1939-03-07 Du Pont Polyamides
US2155067A (en) * 1934-06-01 1939-04-18 Ubbelohde Leo Manufacture of improved products of cellulose and cellulose derivatives
US2191556A (en) * 1936-07-01 1940-02-27 Du Pont Polyamides
US2224693A (en) * 1937-07-28 1940-12-10 Du Pont Formation of threads and the like
US2265559A (en) * 1939-03-09 1941-12-09 Du Pont Dyed regenerated cellulose containing a polyamide

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US950435A (en) * 1908-12-22 1910-02-22 Henri Louis Joseph Chavassieu Process of obtaining proteo-cellulosic products.
US1864426A (en) * 1929-10-25 1932-06-21 Henry A Gardner Delustered regenerated cellulose
US2071251A (en) * 1931-07-03 1937-02-16 Du Pont Fiber and method of producing it
US2155067A (en) * 1934-06-01 1939-04-18 Ubbelohde Leo Manufacture of improved products of cellulose and cellulose derivatives
US2136928A (en) * 1934-12-10 1938-11-15 Ig Farbenindustrie Ag Manufacture of amines of high molecular weight, which are rich in nitrogen
US2191556A (en) * 1936-07-01 1940-02-27 Du Pont Polyamides
US2223916A (en) * 1936-07-01 1940-12-03 Du Pont Polymeric sulphonamide, a process for prepaing it, and a filament made therefrom
US2149273A (en) * 1937-01-13 1939-03-07 Du Pont Polyamides
US2130948A (en) * 1937-04-09 1938-09-20 Du Pont Synthetic fiber
US2224693A (en) * 1937-07-28 1940-12-10 Du Pont Formation of threads and the like
US2265559A (en) * 1939-03-09 1941-12-09 Du Pont Dyed regenerated cellulose containing a polyamide

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2571995A (en) * 1948-02-24 1951-10-23 Gen Mills Inc N, n'-diacyl aryl disulfonamides
US2901813A (en) * 1953-10-20 1959-09-01 American Viscose Corp Textile material of regenerated cellulose containing a polyacrylamide

Also Published As

Publication number Publication date
NL54509C (enrdf_load_stackoverflow)
CH218047A (de) 1941-11-30
BE438483A (enrdf_load_stackoverflow)
FR873775A (fr) 1942-07-20

Similar Documents

Publication Publication Date Title
US2130948A (en) Synthetic fiber
US2339237A (en) Blended polyamides
US3630662A (en) Process of dyeing shaped condensation polymer material in heated two-phase dye liquid
US2265559A (en) Dyed regenerated cellulose containing a polyamide
WO2019237466A1 (zh) 一种天然染料可染的再生纤维素纤维的制备方法
US2416890A (en) Manufacture of fibers and foils
TWI238205B (en) Easy dyeable polyester fiber
US2201741A (en) Polymeric materials
US3104933A (en) Method of dyeing with polyvinyl alcohol ester and quaternary ammonium compounds
US2772943A (en) Process of dyeing wool-polyacrylo-
US3621089A (en) Process for spinning dye-resistant copolyamide filaments
US3635653A (en) Polyester polyamide blend fiber dyed with azo disperse dye
US2206278A (en) Textile and other materials
US2952506A (en) Process for even and level dyeing of filament nylon fabrics
US2253457A (en) Improving the dyeing of textiles
US3492368A (en) Fiber forming linear polyesters with improved dyeability
US3493316A (en) Dyed fiber products
DE1769613A1 (de) Mittel zur Verbesserung der Nassechtheiten von mit kationischen Farbstoffen auf synthetischen Polyamiden erzeugten Faerbungen
US2168335A (en) Cellulosic material and method for preparing same
GB719489A (en) Improvements in the manufacture of articles from superpolyamides
US3738804A (en) Dyeability of melt blend fibers with high electron affinity dyes
US3573244A (en) Method for obtaining acid dye uniformity in polyamides
US3993442A (en) Anionic dyeing of novoloid fibers
US3124412A (en) Continuous- dyeing method for fibrous
US2307973A (en) Dyeings