US2324437A - Yarn production - Google Patents

Yarn production Download PDF

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Publication number
US2324437A
US2324437A US446529A US44652942A US2324437A US 2324437 A US2324437 A US 2324437A US 446529 A US446529 A US 446529A US 44652942 A US44652942 A US 44652942A US 2324437 A US2324437 A US 2324437A
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United States
Prior art keywords
bath
spinning
viscose
zinc sulfate
coagulating
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US446529A
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Soukup Roy
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EIDP Inc
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EI Du Pont de Nemours and Co
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    • 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

Definitions

  • This invention relates to the production of regenerated cellulose yarn from viscose compositions. v More particularly, it relates to an im-- proved process for the spinning of viscose rayon yarn in a coagulating and regenerating bath con-' taining a high concentration (from 8% to 18%) of zinc sulfate.
  • a coagulating and regenerating bath con-' taining a high concentration (from 8% to 18%) of zinc sulfate.
  • spinneret cratering is a term commonly applied to the formation of incrustations and depositions which accumulate on the sp'inneret face and in the spinneret orifices during the production of regenerated cellulose yarn from viscose by the wet spinning process. Under some conditions, especially with spinning baths containing high percentages'offzinc sulfate, these incrustations are apparently caused, to a large extent, by the deposition of acid soluble zinc sulfide at the face of the spinneret. I
  • the sulfuric acid content of the coagulating bath be held within certain limits correlated with the "caustic content of the viscose and-the zinc sulfate content of the coagulating bath.
  • Thesulfuric acid content of the coagulating bath should thereforegbe within plusor' minus 0.6% of that determined by the following equation:
  • A is the percentage concentration by weight of :the'sulfuric acid
  • C is the percentage concentration by weight of the NaOH content ofthe viscose
  • S is thepercentage concentration by weight of the zinc sulfate in the coagulating bath.
  • the spinning of the viscose yarn may beQcarried out with excellent spinning continuity and the resulting yarn will have excellentphysicaicharacteristics.
  • the spinning may be carried out for long periods of time without encountering excessive cratering of thespinnerets.
  • ThefoL lowing table illustratesa number of viscose compositions containing varying percentages of caustic and. coagulating baths containing varying percentagesbfZnSOi, together with the corr'ei lated H2804 concentration to be used in accordance with the present invention. All figures in the table are percentages by weight.
  • the temperature of the coagulating and regenerating bathl is been found to influence spinneret cratering to a certain extent. spinneret cratering is most effectively reduced when the temperature of the bath is maintained substantially above 40 C., for example. if the bath is maintained at about 60 0., or higher. Although lower bath temperatures, such as 4040 C., may be employed satisfactorily when the concentration of the zinc sulfate is in the neighborhood of at high concentrations of zinc sulfate such as 18%, it is generally advisable to use a bath temperature of 60 C. or even as much as 75 C.
  • Example I A viscose composition comprising 7% cellulose and 4% NaOI-I is spun into a coagulating-regenerating bath having the following composition: 6% sulfuric acid, 11% sodium sulfate and 10% zinc sulfate. The bath is maintained at a temperature of 60 C. The yarn is spun at a conventional spinning speed of 3500 inches per minute. The spinning may be carried out for extended periods of time without objectionable spinneret cratering. The resulting yarn has very desirable physical characteristics.
  • Example II A viscose similar to that described in Example I is spun into a coagulating-regenerating bath having the same composition as that described in Example I.
  • the yarn is spun at a spinning speed of 7000 inches per minute. Such speed of spinning is not feasible in a bath containing no zinc sulfate or relatively low percentages of zinc sulfate.
  • the spinning conditions are substantially as good as those set forth in Example I, and the resulting yarns have excellent physical characteristics.
  • viscose containing 7% cellulose and 4% caustic is used for the proweight.
  • the caustic content of the understood that the details set forth in these exduction of viscose rayon in a spinning bath having a high zinc concentration the cellulose content of the viscose may vary between 5%-12% by weight, preferably between 6%-8%, and the alkali content may vary between 3% y (me.
  • the sulfuric acid content of the spinning bath is preferably adjusted to the zinc sulfate content of the bath and the alkali content of the viscose in accordance with the above formula,
  • the zinc sulfate in the coagulating bath may vary between 8% and 18% by weight; however, the greatest advantages of the invention are forthcoming in spinning baths containingrover 10% zinc sulfate. Spinning baths containing over 10% zinc sulfate are useful in the production of yarn having exceptionally desirable physical properties; however, heretofore, spinning baths containing such high concentrations of zinc sulfate could not be readily used due to the tendency of spinneret cratering.
  • the coagulating bath may contain other agents tending to inhibit cratering, for example polymerized ethylene oxide (Carbowax 4000) which may be used in amounts from 0.001% to 1% based on the total weight of the bath. Such additional crater inhibiting materials are not necessary in a bath to attain the objects of the present invention.
  • the present invention provides a process for the production of regenerated cellulose yarn with spinningbaths containing high concentrations of I tions of zinc sulfate. This reduction in spinneret cratering is accomplished in a simple economical manner with a minimum of operational dimculty.

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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

Patent ed July 13, 1943 manmonuo'rlon Roy Soukup, Richmond, Va., assignor to E I. do
Pont de Nemours & Company, Wilmington, DeL, a corporation of Delaware No Drawing. Application June 10, 1942,
This invention relates to the production of regenerated cellulose yarn from viscose compositions. v More particularly, it relates to an im-- proved process for the spinning of viscose rayon yarn in a coagulating and regenerating bath con-' taining a high concentration (from 8% to 18%) of zinc sulfate. [j i The art has long recognized the virtue of coagulating-regenerating baths containing a high concentration of zinc sulfate for use in the spinning of viscose rayon yarn. Yarn produced by the use of such spinning baths hasvery desirable physical characteristics. However, the
extrusion, or spinning, of viscose, of thetype unii versally used in the production of viscose rayon and containing 6% to 8% caustic (calculated as NaOH into an acid spinning bath, containing an appreciable quantity of zinc sulfate, is accom-' panied by the very objectionable phenomenon of spinneret cratering. As the concentration Serial No. 445,529 ZClaims. (c1. lac- It is therefore an object of this invention'to provide an improved process for the spinning of viscose rayoriwith a coagulating-regenerating bath containing a highconcentration ofzinc sulfate (8% to 18% by weight).
It is a further object of this invention to provide a processfor the spinning of viscoserayon with a coagulating-regenerating bath containing a high concentration of zinc sulfate (8% to 18% by weight)whichjprocess will not be subject to excessive spinneret cratering. Other objects of the invention will appear hereinafter. I i
of zinc in the coagulating bath increases, so also i does spinneret cratering increase. Forexample,
when viscose containing 6% alkali and 7 cellulose is spun into a bath containing 8% sulfuric acid, 11% sodium sulfate, 4% glucose, and 15% zinc sulfate at 60 0,, about24% of the orifice area of the spinneret is clogged, incrustated or cratered in four hours. It can readily be seen that under such conditions, sustained spinning of a uniform denier yarn is impossible.
' "Spinneret cratering is a term commonly applied to the formation of incrustations and depositions which accumulate on the sp'inneret face and in the spinneret orifices during the production of regenerated cellulose yarn from viscose by the wet spinning process. Under some conditions, especially with spinning baths containing high percentages'offzinc sulfate, these incrustations are apparently caused, to a large extent, by the deposition of acid soluble zinc sulfide at the face of the spinneret. I
The art has long been faced with the problem of effectively reducing the craters or depositions in the minute orifices of the spinneret; Suclrde posits disrupt the flow of viscose thus causing broken filaments or filaments of uneven v denier to be formed." Numerous additions to the coagulating bath and to-the viscose have been proposed to reduce spinneret cratering and thereby permit uninterrupted and uniform spinning. In most cases, the proposed addenda are expensive. Moreover, the addition of such cratering inhibitors to the viscose or to the coagulating and regenerating bath usually involves additional labor and control difliculties.
'll'lie object's of this invention may be accomplis hed, in general, by spinning alow caustic viscase (3% to 5.5% caustic calculated as NaOH) ,into acoagulating and regenerating bath containing a high concentration of zinc sulfate (8% to,
18% by weightof zinc sulfate).
It is also essential, for the purpose of obtaining good spinning conditions and optimum physical characteristics, of the resulting yarn, that the sulfuric acid content of the coagulating bath be held within certain limits correlated with the "caustic content of the viscose and-the zinc sulfate content of the coagulating bath. Thesulfuric acid content of the coagulating bath should thereforegbe within plusor' minus 0.6% of that determined by the following equation:
A=o.'z5c o.1s+3.a
where A is the percentage concentration by weight of :the'sulfuric acid, C is the percentage concentration by weight of the NaOH content ofthe viscose, and S is thepercentage concentration by weight of the zinc sulfate in the coagulating bath.- For example, if a 7% cellulose, 4% NaOH viscose is to be spun into a bath comprised of 10% zinc sulfate, by the use of the above equation the acid concentration will be found to be 5.8% H2804. The sulfuric acid concentration in the coagulating bath may then vary between 5.8% minus 0.6% i. e.,5.2%, or 5.8% plus 0.6%
i. e., 6.4%. Under such conditions, the spinning of the viscose yarn may beQcarried out with excellent spinning continuity and the resulting yarn will have excellentphysicaicharacteristics.
Furthermore, the spinning may be carried out for long periods of time without encountering excessive cratering of thespinnerets. ThefoL lowing table illustratesa number of viscose compositions containing varying percentages of caustic and. coagulating baths containing varying percentagesbfZnSOi, together with the corr'ei lated H2804 concentration to be used in accordance with the present invention. All figures in the table are percentages by weight.
The temperature of the coagulating and regenerating bathlis been found to influence spinneret cratering to a certain extent. spinneret cratering is most effectively reduced when the temperature of the bath is maintained substantially above 40 C., for example. if the bath is maintained at about 60 0., or higher. Although lower bath temperatures, such as 4040 C., may be employed satisfactorily when the concentration of the zinc sulfate is in the neighborhood of at high concentrations of zinc sulfate such as 18%, it is generally advisable to use a bath temperature of 60 C. or even as much as 75 C.
This effect of temperature on coagulating baths containing a high concentration of zinc sulfate is quite surprising in view of the previously known fact that low temperatures were found to decrease spinneret cratering in processes involvin coagulating baths having low percentages of zinc sulfate. It has been known heretofore that coagulating baths containing, for example, 0.7% zinc sulfate are subject to serious spinneret cratering when the bath temperature is maintained at 55 C., and the lowering, in such instances, of the bath temperature will reduce the spinneret cratering.
The following examples illustrate preferred embodiments of the present invention, it being amples are merely illustrative and not limitative of the invention.
Example I A viscose composition comprising 7% cellulose and 4% NaOI-I is spun into a coagulating-regenerating bath having the following composition: 6% sulfuric acid, 11% sodium sulfate and 10% zinc sulfate. The bath is maintained at a temperature of 60 C. The yarn is spun at a conventional spinning speed of 3500 inches per minute. The spinning may be carried out for extended periods of time without objectionable spinneret cratering. The resulting yarn has very desirable physical characteristics.
Example II A viscose similar to that described in Example I is spun into a coagulating-regenerating bath having the same composition as that described in Example I. The yarn is spun at a spinning speed of 7000 inches per minute. Such speed of spinning is not feasible in a bath containing no zinc sulfate or relatively low percentages of zinc sulfate. The spinning conditions are substantially as good as those set forth in Example I, and the resulting yarns have excellent physical characteristics.
Although, in accordance with the preferred embodiments of the invention, viscose containing 7% cellulose and 4% caustic is used for the proweight. Preferably, the caustic content of the understood that the details set forth in these exduction of viscose rayon in a spinning bath having a high zinc concentration, the cellulose content of the viscose may vary between 5%-12% by weight, preferably between 6%-8%, and the alkali content may vary between 3% y (me. The sulfuric acid content of the spinning bath is preferably adjusted to the zinc sulfate content of the bath and the alkali content of the viscose in accordance with the above formula,
The zinc sulfate in the coagulating bath may vary between 8% and 18% by weight; however, the greatest advantages of the invention are forthcoming in spinning baths containingrover 10% zinc sulfate. Spinning baths containing over 10% zinc sulfate are useful in the production of yarn having exceptionally desirable physical properties; however, heretofore, spinning baths containing such high concentrations of zinc sulfate could not be readily used due to the tendency of spinneret cratering. If desired, the coagulating bath may contain other agents tending to inhibit cratering, for example polymerized ethylene oxide (Carbowax 4000) which may be used in amounts from 0.001% to 1% based on the total weight of the bath. Such additional crater inhibiting materials are not necessary in a bath to attain the objects of the present invention.
The present invention provides a process for the production of regenerated cellulose yarn with spinningbaths containing high concentrations of I tions of zinc sulfate. This reduction in spinneret cratering is accomplished in a simple economical manner with a minimum of operational dimculty.
in a saving in the operating expenses over previously known spinning processes. 1
Since it is obvious that many changes and modifications can be made in the above described details without departing from the nature and spirit of the invention, it is to be understood that the invention is not limited to the above details except as set forth inthe appended claims.
I claim:
1. The process of spinning regenerated cellulose filaments from viscose which comprises extruding viscose containing 3% to 5.5% caustic (calculated as NaOH) into a sulfuric acid coagulating and regenerating bath containing from 8% to 18% zinc sulfate, the sulfuric acid con- V the percentage concentration of the caustic (caltent of the bath being within plus or minus 0.6% culated as NaOH) in the viscose and S repreof that determined bythe equation: 'sents thgu laercentage concentration by weight of the zinc fate. 4-0350 2. The process as defined in claim '1 in which w erei A rep e e percentage eoncentre- 5 the coagulating and regenerating bath is maint on y weight or the sulfuric acid, 6 represents tained at a temperatl'lre of at least 60 0.
- ROY SOUKUP.
US446529A 1942-06-10 1942-06-10 Yarn production Expired - Lifetime US2324437A (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2479218A (en) * 1944-12-12 1949-08-16 Int Paper Canada Process for making rayon filaments
US2581835A (en) * 1946-03-22 1952-01-08 Du Pont Method of spinning viscose
DE946387C (en) * 1943-07-16 1956-08-02 Shozo Tachikawa Process for the production of rayon by spinning viscose
US3116354A (en) * 1957-05-02 1963-12-31 Beaunit Corp Viscose spinning process
US3116352A (en) * 1957-05-02 1963-12-31 Beaunit Corp Viscose spinning

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE946387C (en) * 1943-07-16 1956-08-02 Shozo Tachikawa Process for the production of rayon by spinning viscose
US2479218A (en) * 1944-12-12 1949-08-16 Int Paper Canada Process for making rayon filaments
US2581835A (en) * 1946-03-22 1952-01-08 Du Pont Method of spinning viscose
US3116354A (en) * 1957-05-02 1963-12-31 Beaunit Corp Viscose spinning process
US3116352A (en) * 1957-05-02 1963-12-31 Beaunit Corp Viscose spinning

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