US3420814A - Process for producing artificial staple fibers - Google Patents

Process for producing artificial staple fibers Download PDF

Info

Publication number
US3420814A
US3420814A US473847A US3420814DA US3420814A US 3420814 A US3420814 A US 3420814A US 473847 A US473847 A US 473847A US 3420814D A US3420814D A US 3420814DA US 3420814 A US3420814 A US 3420814A
Authority
US
United States
Prior art keywords
fibers
bath
staple
viscose
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
US473847A
Other languages
English (en)
Inventor
Otto Reichert
Kurt Heuer
Heinz Grotjahn
Hans George Wendlandt
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.)
Akzona Inc
Original Assignee
American Enka Corp
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 American Enka Corp filed Critical American Enka Corp
Application granted granted Critical
Publication of US3420814A publication Critical patent/US3420814A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • D01F11/00Chemical after-treatment of artificial filaments or the like during manufacture
    • D01F11/02Chemical after-treatment of artificial filaments or the like during manufacture of cellulose, cellulose derivatives, or proteins

Definitions

  • a high strength, easy separable and processible rayon staple fiber is produced by spinning continuous filaments into a coagulating bath containing a small amount of formaldehyde and no heavy metal salts, by subsequently stretching the filaments in a second bath at a controlled temperature, by cutting the filaments into staple fiber while still in an incompletely regenerated state, i.e., at a gamma number of 35 to 47, and by depositing the cut fibers into an acid floating bath maintained at a tem* perature above 90 C.
  • This invention relates to a process for the manufacture of regenerated cellulose structures from viscose spinning solutions. More particularly, it relates to a process for producing regenerated cellulosic staple fibers which renders them more suitable for subsequent textile processing and blending with other type fibers.
  • viscose is normally extruded in continuous filament form through a spinnerette orifice into an acid coagulating bath.
  • the bath is composed of an equeous solution containing amounts of sulfuric acid, sodium sulfate, and heavy metal salts such as zinc sulfate.
  • Various viscose modifiers may be added either directly to the viscose or to the coagulating bath to produce desired effects in the final product.
  • the continuous filaments After being stretched and regenerated in the acid bath, are cut into the desired staple length by subjecting the continuous filaments to cutting or breaking devices.
  • the bundles of staple fibers are then washed and tumbled to open the bundles into discret, individual fibers.
  • Rayon fibers which have an appearance similar to those natural fibers of cotton and wool, are then transformed by standard carding operations into yarns which are subsequently woven or knitted into textile articles. Quite often, rayon fibers are blended with dissimilar fibers such as wool and cotton to produce novel textile effects.
  • a high strength rayon staple fiber can be cut from continuous filament to produce easily separable and processible staple fiber components if the filaments are spun into a coagulating bath containing a small amount of formaldehyde and no heavy metal salts, are subsequently stretched in a second bath at a controlled temperature and are cut into staple fibers while still in an incompletely regenerated state, i.e., at a gamma number of 3547.
  • the non-decomposed xanthate in the fibers is evolved as a gas when the fibers are subsequently washed in an acid floating bath.
  • This gaseous release creates a somewhat explosive action to loosen the bunches of fibers so that the individual fibers are separated and may freely shrink and crimp;
  • the present process utilizes the gas evolved during final decomposition, after cutting, to explode the bundles of cut fibers into a highly separated and easily processible staple product.
  • the present process is carried out on a composition of viscose having a high gamma number i.e., about 80, which is spun :at low temperature into a precipitation bath.
  • the bath contains, in addition to the normal amounts of sulfuric acid and sodium sulfate, a low percentage of formaldehyde. For optimum results, the bath should not contain heavy metal salts.
  • the formaldehyde reacts in a normal way to slow down the speed of decomposition of the cellulose xanthate. This enables the threads to be more highly stretched and strengthened in the second bath.
  • the spun threads which may be partially stretched in air, are finally stretched to about 280300% in a second, weakly acid bath having a sulfuric acid content of about 20 g./kg.
  • the second bath must be maintained at a temperature of between 78 and 85 C.
  • After stretching the filaments are cut into staple length while they are still in the partially regenerated state.
  • the staple fibers upon leaving the cutter, have a gamma number between 35 and 47, and preferably higher than 40.
  • the staple fibers leaving the cutter drop into an acid floating bath maintained at a temperature above 90 C. Because of the non-decomposed xanthate remaining in the fibers, :an amount of gas is evolved as the fiber bundles float on the bath.
  • This gaseous liberation explosively separates the bunches of fibers and enables the individual fibers to freely shrink and crimp in the floating bath. It has been found through experimentation that, if the upper gamma number limit of the cut fibers is exceeded, the fibers tend to stick to one another. Thus, by keeping the gamma number below 47 at the cutter, the fibers do not stick in the washing bath.
  • the viscose solution should have a very high gamma number at initial spinning, i.e., about 80. It is well known that the presence of formaldehyde in the spinning bath slows the decomposition rate of the cellulose xanthate so that it becomes, to a great extent, independent of the sulfuric acid and sodium sulfate content of the spinning bath. As a result of the use of formaldehyde, the spinning bath composition can be varied within broad ranges, making it possible to adapt the content of the bath to a given alkali content of the viscose or to particular conditions of the spinning apparatus.
  • the caustic soda treatment of staple fibers is Well known and is used to produce higher elongation. Such treatment is most desirable when the staple fibers are to be blended, during further processing, with fibers of different origin. When the caustic is used, it replaces the usual desultfurizing treatment.
  • the treatment consists of subjecting the fibers to a aqueous sodium hydroxide bath maintained at a temperature of about 25 C. and a concentration of -55 g./kg. These limits can be varied depending on the degree of elongation required. The treatment lasts about 30 to 60 seconds.
  • the strength and swelling value of the fibers of the present invention are not appreciably affected.
  • Spun yarns and fabrics produced from the rayon staple fibers of the present invention compare quite favorably with and are, in most instances, superior to corresponding spun yarns and fabrics of combed American cotton.
  • the following chart shows the comparative data between the staple fiber of the present invention and that of cotton.
  • Example I Beech-wood cellulose was processed in the usual manner to produce a viscose containing 6.2% cellulose and 8.0% NaO-H. The amount of CS added was calculated on the cellulose. The ripening time was chosen to produce a viscose gamma number of 80 at spinning. The viscosity during spinning was 280 seconds (ball fall method) at 20 C. The viscose was spun through a spinnerette having 16,000 orifices 60 microns in diameter into a spinning bath containing g./kg. sulfuric acid, 108 g./ kg. sodium sulfate, and 8.3 g./kg. formaldehyde. The temperature of the bath was maintained at 31 C.
  • the tow leaving the primary coagulation bath was stretched in the air and further stretched in a second bath having an acid content of about 20 g./kg.
  • the tow was stretched a total of 283%.
  • the temperature of the second bath was maintained at 79 C.
  • the tow was cut into staple fibers 40 mm. in length and floated in a hot acid regenerating bath.
  • the gamma number of the staple fibers leaving the cutter was 42.
  • the temperature of the regenerating bath was maintained at C. and the residence time of the fibers in the bath was 60 seconds.
  • the fibers were Washed on a screen belt, desulfurized in a 2.0 g./ kg. caustic soda bath maintained at 65 C., further washed, bleached and lubricated.
  • the staple fibers produced had a 1.25 filament denier, a conditioned strength of 5.7 g./ den. at an elongation of 7%, a wet strength of 3.9 g./ den. at an elongation 7%, and a swelling value of 58%.
  • Example II Viscose prepared as in Example I was spun through a spinnerette having 3,600 orifices of 60 micron diameter into a spinning bath containing 70 g./ kg. sulfuric acid, 80 g./kg. sodium sulfate, and 7.8 g./kg. formaldehyde. Subsequent conditions were the same as in Example I with the exception that the thread was stretched to a total of 364%.
  • the staple fiber produced had a filament denier of 1.38, a conditioned strength of 6.9 g./ den. at an elongation of 6.9%, and a wet strength of 5.1 g./ den. at an elongation of 7.6%.
  • Example III Staple fiber was produced as indicated in Example I. Instead of the desulfurizing treatment, the fiber bunches were subjected to a bath containing 45.0 g./ kg. NaOH at 25 C. for 30 seconds. The fibers were washed, bleached and lubricated in the usual manner. The fibers had a 1.27 filament denier, a conditioned strength of 5.1 g./ den. at 9.3% elongation, a wet strength of 3.5 g./den. at an elongation of 8.9%, and a swelling value of 65%.
  • Example IV A staple fiber was prepared as indicated in Example I. Instead of the desulfurizing treatment, the fiber bunches were subjected to a bath containing 56.8 g./ kg. NaOH at 25 C. for 30 seconds. The fibers were then washed, bleached and lubricated in the usual manner. The fibers produced had a 1.35 filament denier, a conditioned strength of 4.7 g./ den. at 12.9% elongation, a wet strength of 3.4 g./den. at an elongation of 12.3%, and a swelling value of 75%.
  • Example V Viscose was prepared and spun and the tow obtained stretched in the air as indicated in Example I. The tow was then stretched in a tempered acid bath at a temperature of 74 C. The acid content of the bath was g./kg. The tow was stretched to a total of 283%, out into staple fibers, and the fibers were floated in a bath having an acid content of 20 g./kg. and a temperature of 95 C. The fibers leaving the cutter had a gamma number of 50. The fibers were washed, treated with caustic soda as described in Example III, bleached, and lubricated in the usual manner.
  • Example VI Viscose manufactured and spun as in Example I was stretched in air and in a 20' g./ kg. acid bath at 92 C. The tow was cut into staple fibers and float regenerated in a bath at 95 C. having an acid content of 20 g./kg. The gamma number of the fibers at the cutter was 18. After washing, the fibers were treated with caustic soda as in Example III, bleached and lubricated in the usual manner. The resulting staple fiber had a filament denier of 1.28, a conditioned strength of 5.0 g./den. at an elongation of 9.1%, a wet strength of 3.5 g./den. at an elongation of 6 18.9%, and a swelling value of The fibers obtained could not be processed into a yarn because the absence of crimp in the individual fibers prevented the formation of a web on a carding machine.
  • a method of producing a high strength viscose rayon staple fiber having improved separability after cutting and ease of processing into textile yarns and fabrics which comprises the steps of extruding 'a plurality of viscose filaments having a gamma number of about into a first acid coagulating bath free of heavy metal salts and containing a small amount of formaldehyde, pasing the thus coagulated filaments into a second bath having a lower acid content that said first coagulating bath where they are stretched and partially regenerated, cutting the stretched filaments into staple length fibers, and subjecting the cut fibers to a weak acid solution to bring about complete regeneration thereof and to loosen bundles of fibers so that the individual fibers are separated in order to freely shrink and crimp by maintaining the said second bath at a temperature between about 78 C. and C., maintaining the gamma number of the cut fibers between 35 and 47 at the beginning of their regeneration in the weak acid solution, and maintaining the temperature of the weak acid solution above C.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Artificial Filaments (AREA)
US473847A 1964-07-31 1965-07-21 Process for producing artificial staple fibers Expired - Lifetime US3420814A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEV26491A DE1259499B (de) 1964-07-31 1964-07-31 Verfahren zur Herstellung von Regeneratcellulose-Stapelfasern

Publications (1)

Publication Number Publication Date
US3420814A true US3420814A (en) 1969-01-07

Family

ID=7582694

Family Applications (1)

Application Number Title Priority Date Filing Date
US473847A Expired - Lifetime US3420814A (en) 1964-07-31 1965-07-21 Process for producing artificial staple fibers

Country Status (7)

Country Link
US (1) US3420814A (de)
AT (1) AT256326B (de)
BE (1) BE665052A (de)
CH (1) CH443556A (de)
DE (1) DE1259499B (de)
GB (1) GB1121074A (de)
NL (1) NL6509534A (de)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3077374A (en) * 1960-06-06 1963-02-12 American Viscose Corp Method for producing crimped regenerated cellulosic fibers
US3109698A (en) * 1962-04-02 1963-11-05 Courtaulds North America Inc Method for making high tenacity regenerated cellulose staple fiber
US3324216A (en) * 1962-05-16 1967-06-06 Toyo Spinning Co Ltd Viscose spinning process
US3352957A (en) * 1962-11-06 1967-11-14 Chimiotex Process for spinning cellulosic fibers

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT232638B (de) * 1960-04-22 1964-03-25 Chimiotex Verfahren zur Herstellung von aus regenerierter Cellulose bestehenden Gebilden, wie Fäden, Fasern, Schnüren, Folien od. dgl.

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3077374A (en) * 1960-06-06 1963-02-12 American Viscose Corp Method for producing crimped regenerated cellulosic fibers
US3109698A (en) * 1962-04-02 1963-11-05 Courtaulds North America Inc Method for making high tenacity regenerated cellulose staple fiber
US3324216A (en) * 1962-05-16 1967-06-06 Toyo Spinning Co Ltd Viscose spinning process
US3352957A (en) * 1962-11-06 1967-11-14 Chimiotex Process for spinning cellulosic fibers

Also Published As

Publication number Publication date
AT256326B (de) 1967-08-10
DE1259499B (de) 1968-01-25
NL6509534A (de) 1966-02-01
CH443556A (de) 1967-09-15
GB1121074A (en) 1968-07-24
BE665052A (de) 1965-10-01

Similar Documents

Publication Publication Date Title
US2607955A (en) Spinning of viscose
US1989099A (en) Process of improving artificial threads
US5403530A (en) Elongate member production method
US2696423A (en) Viscose modifiers
US5358679A (en) Manufacture of regenerated cellulosic fiber by zinc free viscose process
US2515834A (en) Cellulose filaments and method of producing same
US2284028A (en) Dry spinning process
US4242405A (en) Viscose rayon and method of making same
US3337671A (en) Method of making regenerated cellulose filaments
US3084021A (en) Process for producing regenerated cellulose filaments
US3494995A (en) Method for spinning viscose
US3420814A (en) Process for producing artificial staple fibers
US2098981A (en) Yarn manufacture
US3146116A (en) Cyanoethylation and xanthation of alkali cellulose
US2114915A (en) Process of spinning rayon and the bath used
US3018158A (en) Viscose process
US2315560A (en) Method for producing high strength and crimped staple fibers from viscose
US2792281A (en) Viscose composition and method of spinning
US2287839A (en) Process of spinning
US2339408A (en) Manufacture of artificial materials
US2339316A (en) Wet spinning of cellulose acetate
US2792279A (en) Viscose composition and method of spinning
US3077374A (en) Method for producing crimped regenerated cellulosic fibers
US2347883A (en) Production of cellulosic structures
US2792280A (en) Viscose composition and method of spinning